SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11302010 | in-del | -/T | 0.0629771 | 0.165899 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062001 | GCCATGGAAACATGA[-/T]TTGATTTTAATAGAT | 5521 |
rs11315873 | in-del | -/A | 0.434109 | 0.169127 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846678 | GAGAGACTCTGTCTC[-/A]AAAAAAAAAATTAAT | 5521 |
rs11320746 | in-del | -/T | 0.443866 | 0.157848 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857690 | ACATAACTGTACTAA[-/T]TTTTTTTTTTTTTTG | 5521 |
rs11327150 | in-del | -/T | 0.422 | 0.181428 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680405 | TGTTGTGGGGTGGGG[-/T]GGGGAGGGAGGGATA | 5521 |
rs11335578 | in-del | -/A | 0.286042 | 0.247388 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746384 | TTGGACTGGGAGTTT[-/A]AAAAAAAAAAGTCAT | 5521 |
rs11341457 | in-del | -/A | 0.497359 | 0.0362457 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893883 | CTTAAAGTAAAATTG[-/A]AAAAAAAAAAAAAAA | 5521 |
rs11372355 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649415 | GCATTTTTTTTTTTT[-/T]ACCTTTCTATATATT | 5521 |
rs11375375 | in-del | -/T | 0.498346 | 0.0287064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956235 | CAAATTTCCATTCAA[-/T]TTTTTTTCATATTAA | 5521 |
rs11388336 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699684 | TTTTTTTTTTTTTTT[-/T]AAGAAAAAGCTGGAA | 5521 |
rs11413858 | in-del | -/A | 0.110519 | 0.207473 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659041 | GTCATAGAAATGATC[-/A]AAAAACCTTTTAACA | 5521 |
rs11423195 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074050 | AAAAAAAAAAAAAAA[-/A]GAATTATTTGGAATG | 5521 |
rs11434413 | in-del | -/A | 0.496649 | 0.0407971 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041610 | TGAAGTATTACACTT[-/A]AGAGTTTTTTCCTTA | 5521 |
rs11436255 | in-del | -/T | 0.0770498 | 0.180522 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851823 | TCAAGAGAGTCTTCA[-/T]TTTTTTTTTTAGTGA | 5521 |
rs11448746 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037159 | TTCAGGGAAAAAAAA[-/A]TTATTTTTGCCTAAG | 5521 |
rs11463492 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964442 | TTTAACCTTAGGATA[-/T]TTTTTTTTATCTTGC | 5521 |
rs11464005 | in-del | -/T | 0.396182 | 0.202807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727303 | AGGTGTTTTTTTTTT[-/T]ACTTATTTAAAAATT | 5521 |
rs11464078 | in-del | -/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913553 | CAATGTTTTTTTTTT[-/T]CAAACATCACATTAA | 5521 |
rs11547494 | snp | G/T | 0.00975586 | 0.0691575 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146701106 | AATTCAACCACACGG[G/T]AGAATTACTAGCGAC | 5521 |
rs11738219 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934487 | aatgtcttcttttga[A/G]aagtgtctgttcatg | 5521 |
rs11741457 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845315 | cttttcttttttttg[G/T]ttttttttgagatgg | 5521 |
rs11741933 | snp | C/T | 0 | 0 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055807 | CCATAAGGATTCTCT[C/T]GGCCTTTTAAGCTGG | 5521 |
rs11741940 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813482 | TCAAGTGGAAGCAAC[A/G]CTTAGAGGTATGAAT | 5521 |
rs11742013 | snp | C/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870737 | TTCATAAGGGCCCCT[C/G]TAGATTCCTAAACTC | 5521 |
rs11742231 | snp | C/G | 0.490943 | 0.0666801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984364 | gtgcctgccttattt[C/G]acttagcataatgtt | 5521 |
rs11742465 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786737 | CCCAAACTGGTAGGG[A/T]AAAAAATGAAGACAC | 5521 |
rs11742650 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971891 | ttccttactcagttt[A/C]ccctcttggcaacat | 5521 |
rs11743315 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698317 | AAAAAAAAAAAAAAa[A/T]atatatatatatata | 5521 |
rs11743368 | snp | C/T | 0.495068 | 0.0934692 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053410 | ATTGTTTGGGCTATT[C/T]GTATTTATTTGACTT | 5521 |
rs11744036 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698319 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 5521 |
rs11744339 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598518 | tatatccagactcac[A/G]ttgaagtgtctacct | 5521 |
rs11744888 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934321 | aaagtgttcctattt[C/T]tccacatcctctcca | 5521 |
rs11745921 | snp | C/T | 0.435004 | 0.168147 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971252 | AAAGATCTCTTTCCC[C/T]CTCGGCATATTCCAG | 5521 |
rs11746185 | snp | A/C | 0.439537 | 0.163021 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056741 | TTTAAGGACATGACC[A/C]ACCACAAGATATAAG | 5521 |
rs11747894 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837555 | gagacacatatgtgg[G/T]ttaaaattttctagc | 5521 |
rs11748210 | snp | A/C | 0.499502 | 0.0157669 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808852 | TTGGAGTTTGCAATC[A/C]ACATTTATCTCTATA | 5521 |
rs11748264 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934267 | gccacactgacttcc[A/C]caatggttgaactag | 5521 |
rs11748312 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038920 | TGCTTCTTTAAAAAG[C/T]ATAATGAAGTAGGAG | 5521 |
rs11748900 | snp | A/G | 0.460925 | 0.134204 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795768 | AAAACGTCAGGTTGT[A/G]CAACTTAAATACAAA | 5521 |
rs11749302 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789400 | GTATTAATAATATAG[C/T]TATCACACATGCTTA | 5521 |
rs11750417 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845300 | ATTTCTTTTCttttc[C/T]ttttcttttttttgt | 5521 |
rs11750446 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845305 | ttttcttttcctttt[C/T]ttttttttgtttttt | 5521 |
rs11750453 | snp | C/T | 0.476227 | 0.106402 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990905 | aggattaaaaatagg[C/T]aaaaaacatgaatag | 5521 |
rs11948136 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845532 | tgttgggattacagg[C/T]gtgagccaccacacc | 5521 |
rs11948170 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776656 | ataaaattggacttc[A/G]ccgaaataaaaattt | 5521 |
rs11949219 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014234 | tagaaagtcaggaaa[A/C]aacaggtgctggaga | 5521 |
rs11949312 | snp | C/T | 0.166506 | 0.235645 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746640 | GAATTTTCTTCCTTG[C/T]GCTACCCCTGCTATC | 5521 |
rs11949763 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727781 | AAGTTGTGCAGATCT[C/T]TAAAACTTCTTCTTC | 5521 |
rs11951894 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599614 | AGCACCCTGAACACA[C/T]CTCATTTCTCTTGAC | 5521 |
rs11952122 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996494 | ACCACACTGAGAAGA[C/T]GGGATTGTTACCCTG | 5521 |
rs11952352 | snp | C/T | 0.161267 | 0.233723 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655499 | GTTTTTTAAACACTT[C/T]AGCAGTTCCTCAGTG | 5521 |
rs11952689 | snp | A/C | 0.0955749 | 0.196603 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868024 | CAGATCATGTCATTG[A/C]GAGCTTAACCTCATT | 5521 |
rs11952831 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862339 | CTACTGTCCTTTGTA[C/T]GGTAAACTAGAGGGA | 5521 |
rs11952955 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696076 | ATTTTTTCCCATCCC[C/T]CCGCCAACAAAGTAG | 5521 |
rs11953078 | snp | C/T | 0.401037 | 0.199218 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967889 | CAGAAATATCCTCAC[C/T]GCAGCAAACAAGCTA | 5521 |
rs11953229 | snp | C/T | 0.358728 | 0.225118 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661653 | ATGCTCTTTGTGTCA[C/T]TGACTTCTTTTGGCC | 5521 |
rs11953321 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722189 | CCAGATACTatttac[C/T]gaagacctgctatat | 5521 |
rs11953683 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973170 | GATTTGATTCTTTTT[C/T]TTTTTCTTGTGGTTA | 5521 |
rs11954559 | snp | A/C | 0.277334 | 0.248501 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608238 | CTAGGACTGGTAGCA[A/C]CATGAGATCATGTAG | 5521 |
rs11955902 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730841 | ggactaatacaGGGA[A/G]ATTAAACTTATATCA | 5521 |
rs11956043 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727670 | cccgtaagtcaaaaa[A/G]aaattttaaaaaaaT | 5521 |
rs11957208 | snp | A/G | 0.236724 | 0.249647 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669185 | TTGCCTCTAATCTAG[A/G]AATACAATTATGTAC | 5521 |
rs11957376 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706367 | CCAGAGCCTGTGAGG[C/T]CCCCATAGGCCAAGC | 5521 |
rs11957997 | snp | C/T | 0.352938 | 0.227824 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838183 | AGTCTCTAATACTTA[C/T]ATTGTGACAAACTTT | 5521 |
rs11958150 | snp | A/T | 0.361474 | 0.223771 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657013 | AATGTTGCTGTCATT[A/T]GGCTTATTTGGTGAC | 5521 |
rs11958151 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730456 | ttgaaatgtggagac[A/G]tgaaatttggagggg | 5521 |
rs11958158 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832761 | aaatgcttaccattg[G/T]gttatgattgcctac | 5521 |
rs11958187 | snp | A/G | 0.498652 | 0.0259235 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055600 | GCATCAGCAGAACCC[A/G]TGGGAAGTCAGACAC | 5521 |
rs11958823 | snp | G/T | 0.0615197 | 0.164406 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730609 | gtctttcccgtgcta[G/T]tctcataatagtgaa | 5521 |
rs11958882 | snp | A/G | 0.339656 | 0.233371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670686 | tttttagtggagacg[A/G]ggtttcatcatgtca | 5521 |
rs11958907 | snp | C/G | 0.357664 | 0.225629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670716 | agccaggctggtctc[C/G]aactcctgacttcaa | 5521 |
rs11959699 | snp | C/T | 0.476227 | 0.106402 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014666 | ccgcatattctcact[C/T]ataggtgggaattga | 5521 |
rs11960073 | snp | A/C | 0.166506 | 0.235645 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644396 | AACTGTGATGCGAAT[A/C]CAATGTATAGACAGC | 5521 |
rs11960236 | snp | A/G | 0.358303 | 0.225323 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667324 | ACAGCAGGAATAGGC[A/G]TGCGCGCGCACACAC | 5521 |
rs12055312 | snp | C/T | 0.345925 | 0.230864 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834795 | TTCCCCTTCAAGCAG[C/T]CCTCAGTGTCTATTT | 5521 |
rs12109778 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032245 | ggctaaggacatgaa[C/T]agacaattctcaaaa | 5521 |
rs12110022 | snp | A/G | 0.108755 | 0.206276 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770854 | TCAAGCAGTTGCAGA[A/G]GGGATTTGCAGCTCT | 5521 |
rs12152738 | snp | A/G | 0.49621 | 0.0433651 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079964 | TAAATATGTGCAATC[A/G]TATCAATTTCTTTTA | 5521 |
rs12186575 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782819 | AGGGAGAGGAAACAG[A/G]AGAAAGAAGGAAAAA | 5521 |
rs12187728 | snp | A/G | 0.477345 | 0.103991 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993724 | CTCCTAGCTCACAAC[A/G]GGGGCTCAATAAATG | 5521 |
rs12188535 | snp | C/T | 0.456685 | 0.140646 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981603 | cttgtatccttttcc[C/T]aacttatctcaatag | 5521 |
rs12513869 | snp | A/G | 0.390651 | 0.206682 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817818 | GACCAACGGTCAAAT[A/G]TTTCTGCCACCCATT | 5521 |
rs12514241 | snp | A/T | 0.478603 | 0.101197 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019394 | AAGAAAGTTAATAAG[A/T]TCATCCTTGCAATTT | 5521 |
rs12514995 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823430 | tcttgatctcctgac[A/C]tcgtgatctgccctc | 5521 |
rs12515810 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017987 | GTAGTTTTGCATGTA[A/G]GAAATCTTCCAGGCC | 5521 |
rs12515824 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018041 | CACACATGCATGCGC[A/G]CGCACACACACACAC | 5521 |
rs12515825 | snp | A/G | 0.375 | 0.216506 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018043 | CACATGCATGCGCGC[A/G]CACACACACACACAC | 5521 |
rs12515940 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958375 | ATCACTAGTAGATCT[A/G]CCTCCATGAGCACTT | 5521 |
rs12516151 | snp | A/G | 0.369142 | 0.219784 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817517 | CAAATTGATATTTCC[A/G]TCATCTCACACAATT | 5521 |
rs12516445 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812781 | ttaatgtgtgtgtgt[A/G]tgtatatgtgtgtat | 5521 |
rs12519188 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646233 | TCTTTATTTTTACTC[A/G]ATATGGGCCTATTTA | 5521 |
rs12519616 | snp | A/G | 0.384785 | 0.210554 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831281 | acaggtggattacct[A/G]aggtaagaagtttga | 5521 |
rs12520019 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064110 | TCTGTTTGGCCTGCA[A/G]AGTATTGTATTTTCT | 5521 |
rs12520459 | snp | A/C | | | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766733 | GAATGCTACCACAAC[A/C]CCGTGGGCCCTACGG | 5521 |
rs12521366 | snp | A/G | 0.206336 | 0.246157 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065793 | TTTGGGAGGGCTTTC[A/G]GAGGAAGAAACTGGA | 5521 |
rs12523317 | snp | A/G | 0.429987 | 0.173507 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036682 | ACCAGAATCTCTTGT[A/G]TTTTTGACTTTTTAA | 5521 |
rs12652549 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053183 | tgacatgtaacagag[C/T]taagattcaaaacct | 5521 |
rs12653494 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676500 | caccgcctctgccta[A/G]aacattctttctgct | 5521 |
rs12654507 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044361 | TTGTGAGGGGGTTCA[G/T]GGCACCTGTGAAGGG | 5521 |
rs12655613 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951181 | ATCTCTTTTTTGTTT[G/T]TTtttttttaatatc | 5521 |
rs12656540 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734219 | caccaccatacctgg[A/C]taatgtttttatttt | 5521 |
rs12659113 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989849 | tatacatagaaaatc[C/T]taaagactccactaa | 5521 |
rs12659576 | snp | C/G | 0.416055 | 0.186885 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915408 | ATACATCATCTTCCC[C/G]TCCTACTCAATAAAT | 5521 |
rs12659673 | snp | A/T | 0.28052 | 0.24813 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704855 | ATGTGAGGCTAATGA[A/T]TGTGAGGCTTACGGA | 5521 |
rs12659795 | snp | C/T | 0.236434 | 0.249632 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684585 | AGAAATGGCAATGCA[C/T]ATCCTGTATGCCTCA | 5521 |
rs12659797 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708107 | acgcctataatctca[C/G]cactttgggaggctg | 5521 |
rs12717949 | snp | C/G | 0.395818 | 0.203069 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873733 | ttcctgcctcagcct[C/G]ctgagtagctgggat | 5521 |
rs13158245 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762332 | cagcattctctgaag[C/G]catcagtttccccat | 5521 |
rs13158389 | snp | C/T | 0.47517 | 0.10862 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974781 | TGCAAGCTCCGCCTA[C/T]GGGTTCACGCCATTC | 5521 |
rs13159496 | snp | A/T | 0.476487 | 0.105846 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983534 | tctagatattacatt[A/T]tataaacaaaagtta | 5521 |
rs13160576 | snp | A/G | 0.0186899 | 0.0948454 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862575 | GAGGCAGGCCTTGCA[A/G]GTACCAGGGAAGGGG | 5521 |
rs13162831 | snp | A/G | 0.477768 | 0.103061 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998749 | AATTAACCAGAAATA[A/G]ATTAAAATGACTTTA | 5521 |
rs13163144 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768362 | GCCACCATGCAAGTC[C/T]TAAGAACTGGTTGTA | 5521 |
rs13163875 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595043 | GGGTATTTGAAAAGC[C/T]CTGAGTTATTTGGAC | 5521 |
rs13164602 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675421 | AAATACCCTGGTATC[A/C]TGGACTGTGGGATAG | 5521 |
rs13165086 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598227 | actaaatccaagttc[A/G]tagtcttctgtactt | 5521 |
rs13165556 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053915 | CACTATGTCCCAGAG[C/T]CTCCTCCACGATGTT | 5521 |
rs13166047 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898982 | aggaaacaacaggtg[A/C]tggagaggatgtgga | 5521 |
rs13169720 | snp | G/T | 0.451259 | 0.148307 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017508 | AAGGATGAAGTTTAC[G/T]TAGAGAACAGAATTC | 5521 |
rs13170307 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079399 | taaaatgggatatat[A/T]atatATATAATATAC | 5521 |
rs13170431 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079420 | TATAATATACACACA[A/C]ACACACACACATTTt | 5521 |
rs13170894 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929731 | TATAAATAAAATAAG[C/T]AGCAGTTTTGCGTGT | 5521 |
rs13170982 | snp | A/G | 0.498714 | 0.0253268 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958180 | GGCCCCACCCTTTCA[A/G]ATTCCAGGCACCATC | 5521 |
rs13172310 | snp | A/G | 0.477853 | 0.102875 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003743 | gacctgtgttctaga[A/G]ggactaaggagaatt | 5521 |
rs13172448 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983204 | ttttttttttgagac[A/G]gagtcttgctctgtc | 5521 |
rs13174253 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079398 | ATAAAATGGGatata[A/T]aatatatataatata | 5521 |
rs13174342 | snp | A/G | 0.396364 | 0.202676 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934009 | ctacaaaggacatga[A/G]ctcatcgttttttat | 5521 |
rs13174372 | snp | A/G | 0.443714 | 0.200191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934071 | cacattttcttaatc[A/G]agtctatcattcttg | 5521 |
rs13177689 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062240 | aggagcaataggctg[G/T]accatctaggtttgt | 5521 |
rs13178259 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595042 | TGGGTATTTGAAAAG[A/C]TCTGAGTTATTTGGA | 5521 |
rs13178283 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013864 | caaaagcaatggcaa[C/T]gaaagccaaaattga | 5521 |
rs13178911 | snp | C/T | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919177 | gtcaaaacccatgtt[C/T]acaattactctacag | 5521 |
rs13181792 | snp | C/T | 0.485187 | 0.0847778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966716 | CTGGGCCTGGCACAG[C/T]GTAGGAGCACAAAAA | 5521 |
rs13181991 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783907 | GTTATTAACTTATCA[C/T]ATTAGAATATCAAGG | 5521 |
rs13182446 | snp | C/T | 0.324382 | 0.238678 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932227 | GTATTTAAGGTTTAT[C/T]AAGGTATCAGCCTGT | 5521 |
rs13182712 | snp | G/T | 0.483053 | 0.0904792 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967932 | AGGAAAATTTTCCCT[G/T]CAAGGTCTGGACATT | 5521 |
rs13183391 | snp | G/T | 0.464947 | 0.127663 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038239 | ATCCTTGTTCTCATA[G/T]AGCTTACATTCTTAT | 5521 |
rs13183604 | snp | A/G | 0.478437 | 0.10157 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975904 | atatataatttgcaa[A/G]tattttctcccattc | 5521 |
rs13183997 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999038 | aaaaaaaaaaaaaaa[A/G]GAGTCAATCTCTGGT | 5521 |
rs13184277 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962963 | AAGGCACTCAGACTT[C/T]CTTAGTGGAGCTGAA | 5521 |
rs13185031 | snp | C/T | 0.477175 | 0.104362 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008498 | CTGTTTGTCCTAACT[C/T]AATAGGACTTTCCAC | 5521 |
rs13185140 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686762 | GAGAAAAAGAATACC[C/T]CCAGGCTTACCCTGC | 5521 |
rs13185770 | snp | C/G | 0.481319 | 0.0948228 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002971 | ctgaaaaagaggcag[C/G]tcatttttttctgca | 5521 |
rs13187365 | snp | C/T | 0.478437 | 0.10157 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975786 | tttgtatattttatt[C/T]ggcaaaatatctatt | 5521 |
rs13187668 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806467 | TAGAATCTTGCTTGT[A/G]ATATAAAAAAAAGAA | 5521 |
rs13188091 | snp | C/G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675377 | CTTTCATTCAATCTT[C/G/T]GTTTTTATGTTCCCC | 5521 |
rs13188774 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079418 | tATATAATATACACA[A/C]AAACACACACACATT | 5521 |
rs13189293 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993890 | AATAGTTAGTAGCTG[G/T]TCTCTAAGGATCCAG | 5521 |
rs13190051 | snp | C/G | 0.393434 | 0.20476 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886058 | aattagataggggcg[C/G]ccgggcgcggtggct | 5521 |
rs13340393 | snp | G/T | 0.398354 | 0.201224 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724889 | AACTTTTGACCTTAA[G/T]AGGATGATTGACAGT | 5521 |
rs13354546 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028172 | GGCTTTACCTCTTAA[C/T]AGAAGACCTTGGCTC | 5521 |
rs13354638 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712934 | TACGTGTAAAGTACT[A/T]TTCCAGATATTAAAG | 5521 |
rs13356903 | snp | A/T | 0.0670745 | 0.170406 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998326 | TTCAATCGTCTTTGC[A/T]GCTGGGAGACTGAAG | 5521 |
rs13357239 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756433 | GGAAAGAATACACTA[C/T]GGCAGATGTGAGGTT | 5521 |
rs13358456 | snp | A/G | 0.383824 | 0.211166 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829983 | TCAGAGGTAAAATAG[A/G]TATTGTGAGAATACC | 5521 |
rs13359973 | snp | C/T | 0.397271 | 0.202018 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011937 | tgaagcccacttgat[C/T]gtggtggataagctt | 5521 |
rs13361498 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884417 | ACTTGTGAGTAATTG[C/T]TTTTATAGGGCTCCT | 5521 |
rs13362410 | snp | A/G | 0.408188 | 0.193589 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007157 | ctggtcctttcactg[A/G]cctaaagagttccca | 5521 |
rs13435944 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736431 | atctagttgttatta[C/T]taccatcattttaaa | 5521 |
rs13435960 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040402 | AATTTCCAAACAGAA[C/G]ACTAGAAATACTGCA | 5521 |
rs13436115 | snp | A/G | 0.14665 | 0.227637 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736424 | tcttatgatctagtt[A/G]ttattattaccatca | 5521 |
rs17096628 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965041 | GAATTGATGGGGCTA[C/T]ACACCAGAACATCAT | 5521 |
rs17104929 | snp | C/G | 0.0836354 | 0.186609 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625381 | GTCAACTACTCTTTA[C/G]TGTTGGCTTTTACAT | 5521 |
rs17104941 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640042 | TTAGAGTTTAGATGC[A/G]GTACAAGCAAATGCA | 5521 |
rs17104949 | snp | C/T | 0.116838 | 0.211584 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641808 | CAATTCGTGGCTCCA[C/T]GTATAATCTTGAAAA | 5521 |
rs17104961 | snp | A/G | 0.180064 | 0.240019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645652 | CTTAATTAGGGAATC[A/G]ACTCTAACAGGGCTT | 5521 |
rs17105086 | snp | C/T | 0.361894 | 0.223562 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668814 | TTCTGTACTGCTTTC[C/T]GACCTCTTTGCCCCC | 5521 |
rs17105166 | snp | G/T | 0.19334 | 0.243495 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688007 | TCTGATTAATATCAC[G/T]TCAGCTCATTCTCTG | 5521 |
rs17105175 | snp | C/G | 0.376791 | 0.215463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689762 | ATTCAGAGCATCAAG[C/G]CTGGATTTATGCCAA | 5521 |
rs17105189 | snp | A/G | 0.204189 | 0.245767 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697130 | ATGTATATTCCTCAT[A/G]GACTCACATATGAGA | 5521 |
rs17105194 | snp | A/C | 0.371177 | 0.218669 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710058 | CCCACTTGCTTGATT[A/C]CTAGTATTAAGATGA | 5521 |
rs17105201 | snp | C/T | 0.428484 | 0.175052 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711691 | ACTCGATTTAATGAA[C/T]GCCTATTATGTGCAT | 5521 |
rs17105251 | snp | C/T | 0.282895 | 0.247826 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718165 | TAGCCCAATGTTTGA[C/T]ACATAGTAGACATGC | 5521 |
rs17105270 | snp | A/G | 0.229429 | 0.249152 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723328 | TCCCGTCAGTCATTC[A/G]GCTTTCCTTTAAACT | 5521 |
rs17105275 | snp | C/T | 0.3748 | 0.216622 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723721 | CTTTTCTAAAACACA[C/T]GCCCTGATCTTCTAA | 5521 |
rs17105284 | snp | C/G | 0.352504 | 0.228019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724718 | AGCTGGGCTGATCTT[C/G]ACATATTTAATATCT | 5521 |
rs17105298 | snp | A/C | 0.31357 | 0.241783 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726352 | GAGGACAAAGAGTGG[A/C]ACACAGGACTTTTTG | 5521 |
rs17105304 | snp | C/T | 0.193028 | 0.243422 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726975 | AAGGAGGCGTTTCCA[C/T]AAGAAGGGACAACTG | 5521 |
rs17105319 | snp | C/T | 0.146985 | 0.227789 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734719 | TGCTGTCAAATTGGA[C/T]AAAATCAATGTCTAC | 5521 |
rs17105323 | snp | C/T | 0.146985 | 0.227789 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735203 | AAATAACAGGTAAAA[C/T]CAGGCTGCCAAATGA | 5521 |
rs17105326 | snp | C/T | 0.26818 | 0.249338 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738429 | AAAATCTTAGCTTCA[C/T]AGAAAAACTAGTTGG | 5521 |
rs17105328 | snp | A/T | 0.290706 | 0.248569 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738462 | GTGACTTTAAACGTC[A/T]TCTTATTTTATTCAT | 5521 |
rs17105330 | snp | C/T | 0.382085 | 0.212258 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745475 | CTGTTAAGTGAAAGA[C/T]GAATGTTAGTTATTG | 5521 |
rs17105387 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792386 | TTCATGCATTCATCC[A/G]TTCAACATGTAGTTG | 5521 |
rs17105400 | snp | A/G | 0.330016 | 0.236849 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822909 | AACTAAAAGCAATGC[A/G]GTCCCCAAATTTAGA | 5521 |
rs17105402 | snp | C/T | 0.386884 | 0.209196 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825170 | GTTTCACAGAGCCGA[C/T]GTTATCACATAGACA | 5521 |
rs17105409 | snp | A/G | 0.359364 | 0.22481 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827981 | GAAAAAGAATTGGGA[A/G]TCTCCATGGCCTAGT | 5521 |
rs17105517 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860599 | CCTCTCCAGTAGGTC[C/T]GATAGTCACTAATCC | 5521 |
rs17105535 | snp | C/T | 0.3752 | 0.216391 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863084 | GTCCTGGTGGGTGCT[C/T]ACCAAGTTTCTGATC | 5521 |
rs17105550 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866312 | AATTATTGTATTGTA[C/T]GTCAGTTTGCTCTTA | 5521 |
rs17105596 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880415 | GGATGAGCTGTATCT[A/G]TCACCGAGGTTCCAA | 5521 |
rs17105615 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882695 | TGTCAGACACTGGGA[C/T]AGGATTATAGATTCA | 5521 |
rs17105709 | snp | A/C | 0.226484 | 0.248892 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920491 | GTCATTAAATGAGTT[A/C]TTCAGGGAGGGCAGT | 5521 |
rs17105742 | snp | A/G | 0.395635 | 0.2032 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936469 | CCTTGTAAGCAGGAA[A/G]AGAAAAAAAAAAAAA | 5521 |
rs17105766 | snp | A/T | 0.339656 | 0.233371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953081 | AGCTAAATGGCTGAT[A/T]CTCAGTTACATGCCC | 5521 |
rs17105785 | snp | A/C | 0.268452 | 0.249318 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958310 | TCTTGATTTTCACAC[A/C]AAAGCCTTCAATCCC | 5521 |
rs17105787 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962180 | TGAGCCCTAGAAACA[C/T]TTAGGCTGTGAAGCA | 5521 |
rs17105791 | snp | A/C | 0.34659 | 0.230587 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965284 | AGCTATAGAATTCTT[A/C]TACATACACATAATT | 5521 |
rs17105806 | snp | A/C/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994347 | TTCAACCTATATTTC[A/C/G]TGAGTAACAGTTCAG | 5521 |
rs17105814 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995498 | GTTTGAATTCAGGAA[C/T]GATATGGGAATTTCT | 5521 |
rs17105820 | snp | C/T | 0.084364 | 0.187256 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008941 | AAGTGATATTCACAT[C/T]GTCCTTAGATTGCAC | 5521 |
rs17105835 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040953 | CGATTCTTTATAGTG[C/T]ATCCTTGAGGTGTTT | 5521 |
rs17105849 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052607 | GAAAAGAAAAGCAGC[C/G]CAAAAGTCTATGGTG | 5521 |
rs17105854 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053329 | CTAATTAGGATGGTT[C/G]TATCCCCTAAGAAGC | 5521 |
rs17448288 | snp | A/T | 0.0505692 | 0.150756 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625179 | GTTCTAGTTTTCCAA[A/T]TTGTAAAAATATTGC | 5521 |
rs17448496 | snp | A/G | 0.279991 | 0.248195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636052 | CACCATTCTTGATCT[A/G]GGTTCCAAATTATCC | 5521 |
rs17456511 | snp | A/G | 0.32627 | 0.238082 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694259 | GCTCTGAATTGTGCC[A/G]TCACCCTGGCTTGCG | 5521 |
rs17457697 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732608 | ATTTTTACCACAAAC[A/G]ATAACAGCATTAATA | 5521 |
rs17458178 | snp | C/T | 0.102726 | 0.202016 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757620 | CTTGCACAGAGGACA[C/T]AGGGGTCTTCCCTGG | 5521 |
rs17462154 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904671 | TCCTGTAGCCTCAGT[A/G]TAGAATGAAAGAGAC | 5521 |
rs17463413 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965421 | TGGGAAAGTGCAGAG[A/G]GTGGTTCAGGTGAAC | 5521 |
rs17464441 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059266 | TTCTTTGGGATTATA[A/G]AGCCCCAAAAAGTCA | 5521 |
rs17514124 | snp | C/G | 0.0505692 | 0.150756 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621591 | TGATCTCACCAACCA[C/G]AGAGAATTAACCAGA | 5521 |
rs17514534 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642437 | CTTTTTATGAAAACA[A/G]AAGTCCAGCATGATA | 5521 |
rs17516662 | snp | C/T | 0.499994 | 0.00179711 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717691 | TTTGGTAGGTCATCA[C/T]TAAGAACACTTTGTG | 5521 |
rs17524553 | snp | A/T | 0.0830503 | 0.186085 | missense, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081128 | TGTCCTGGGTGAGTG[A/T]CCCAATTCCTGAAAA | 5521 |
rs28364819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056206 | TCTCCAGGGCAGAAC[A/G]CTATGCTGTCTTTGT | 5521 |
rs28384073 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812783 | AATGTGTGTGTGTGT[A/G]TATATGTGTGTATAT | 5521 |
rs28396701 | snp | C/T | 0.333722 | 0.235565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813551 | GGCACTGGCAGCTGT[C/T]CGGGTCCTCAGTGAG | 5521 |
rs28396733 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703430 | TTCTGCTTACATGCA[A/G]TCTATGCCCTTTCAC | 5521 |
rs28404917 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828260 | TTACTTTTACTTTTT[A/T]TAAAAAAAAAAAAGA | 5521 |
rs28413768 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033611 | GATGGAGACAGATGG[G/T]GGGTTGGGAGGTAAT | 5521 |
rs28415145 | snp | C/T | 0.38555 | 0.210062 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830723 | GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC | 5521 |
rs28460525 | snp | A/G | 0.33303 | 0.235809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667330 | GGAATAGGCGTGCGC[A/G]CGCACACACACACAC | 5521 |
rs28463964 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853749 | AAATAAAATATCTAC[C/G]ATAGACTTTTTCCTG | 5521 |
rs28528273 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731493 | TGCATTTCTGTATAT[A/T]CTTCTCCTTTCCCTC | 5521 |
rs28573230 | snp | A/G | 0.0640965 | 0.167152 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765457 | TGCATTTGAAGAACA[A/G]TGCCCAGAACATGGA | 5521 |
rs28582634 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675094 | CAGCCTCCAAGTAGC[G/T]GGGATTACAGGCATG | 5521 |
rs28676990 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697973 | CCAAACAGGAATTCC[A/C]CCTACCATTAGTAGA | 5521 |
rs28686836 | snp | G/T | 0.105924 | 0.204309 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713873 | AATGTGAGAGGTTTA[G/T]AAGTACAGATGTTGA | 5521 |
rs28704742 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698182 | ACAACAGATTAAATC[A/C]CAGTAGCCAACTGTA | 5521 |
rs28719805 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926252 | TTCTGATATTTTTTT[C/T]CCCTTTATGGTGGTT | 5521 |
rs28726196 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661144 | CTGGGCAGTGTCTGG[A/G]GGTATTTTTGGTTGC | 5521 |
rs28763718 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609918 | ACGAGGCTGGGGGAG[A/G]GGCGCCCGCCATTGA | 5521 |
rs28767768 | snp | C/T | 0.234982 | 0.249549 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609731 | CAAAGAAAGGGGTGA[C/T]GGACGCACCTGGAAA | 5521 |
rs28774676 | snp | C/T | 0.0584853 | 0.160693 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863932 | AAGTGGACTAAAAAT[C/T]GCTCACTGAAAATAT | 5521 |
rs28813131 | snp | C/T | 0.373598 | 0.21731 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985577 | ACTTTGAGTCAACAC[C/T]ATAAAGGCCATATAG | 5521 |
rs28884884 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609501 | GGAGCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 5521 |
rs33922020 | in-del | -/ATTTTC | 0.307176 | 0.243374 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638051 | GGTCATGTCTTATTT[-/ATTTTC]ATCTCTGGATGTTTT | 5521 |
rs33961672 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938780 | TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTCC | 5521 |
rs33981708 | in-del | -/TATATATATATATATATATATATATATATA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772403 | ATATATATATATATA[lengthTooLong]CTTATTTCTAAATAC | 5521 |
rs33999433 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922901 | GAGGTTCTCTCTCCC[-/C]TGTTGGAGATTCATG | 5521 |
rs34002772 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744577 | CATGTGTCACCAGGG[-/G]AACCATCCTGTGTGC | 5521 |
rs34005036 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886819 | ATTATCATTTTAAAC[-/T]TTTTTAGTAAAAAAA | 5521 |
rs34005745 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662395 | ACAAATTGACTTAAG[-/G]ATTGACATTTCAGGG | 5521 |
rs34021321 | in-del | -/A | 0.487995 | 0.0765403 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897809 | AACATAGAGAATAAG[-/A]AAAAAAAAACATGGA | 5521 |
rs34028029 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027179 | AGTCAGACAAAAAGG[-/G]AACGCATACAATACA | 5521 |
rs34030045 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036356 | GATCTCATTCCTTTT[-/T]ATGGCTGCACAGTAT | 5521 |
rs34035618 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671314 | AATAGAAAAACACGT[-/G]CTCTGTCCTTAGGTT | 5521 |
rs34040465 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685130 | TACATGGAAAAGTCC[C/T]GTACATCAGATGTTG | 5521 |
rs34050073 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691135 | GCACTCACCCGCAGG[-/G]TTGTGATGGTGGCAG | 5521 |
rs34065011 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698292 | ATGATAGTCACTAGC[A/C]CCTCTGAAAAAAAAA | 5521 |
rs34096568 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620940 | CAGTGCTGAACTCCC[-/C]AAGCTGCCCCGTTTC | 5521 |
rs34097720 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767365 | GGTCAGAAATGCTCC[-/C]TGGTACCATATTCCT | 5521 |
rs34098668 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034285 | GGCCACTCAATCTTT[-/T]CATTATCACACTATC | 5521 |
rs34108712 | in-del | -/GTTTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845320 | TTTTTTTTGTTTTTT[-/GTTTTT]TTTGAGATGGAGTCT | 5521 |
rs34131720 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774030 | AGCAAAACAAGAGAG[-/G]AAAACTGTATATTTT | 5521 |
rs34132600 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938962 | ATTTTTTGTATTTTA[A/G]TAGAGACAGGGTTTC | 5521 |
rs34155726 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074558 | GGCTACAAGTCTTTT[-/T]ACTGCTTTGAGACAA | 5521 |
rs34156552 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692551 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 5521 |
rs34172649 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742817 | CCTTATAAAAAGGGG[-/G]AAACTGAAACACAGA | 5521 |
rs34191998 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806864 | TGAGGAAGTATAAAA[-/A]GTGCCCCCGACAGGG | 5521 |
rs34201981 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864644 | GGGCAACTGAATCCC[-/C]AGGGTACAAACTACT | 5521 |
rs34208864 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799591 | AAAGTGCTGCAACCC[-/C]AAAAGAACAGAGGTG | 5521 |
rs34215904 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763264 | CAGGGCACAGACAGG[A/G]AAATGTGCTATTTGA | 5521 |
rs34231856 | in-del | -/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602004 | AAGTTGGATGTATAG[-/T]AGTATATCTCGATAT | 5521 |
rs34247998 | in-del | -/A | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619647 | GAGCGTGTGATCAAA[-/A]CATACGTCCTCTGTA | 5521 |
rs34260296 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982204 | TAATCTATACATTTA[-/A]GTGCTATAAATTTGC | 5521 |
rs34269274 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832408 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCAC | 5521 |
rs34270221 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722414 | GCTTACTGAGTTATC[-/C]TGCTGATGAATCAGA | 5521 |
rs34277498 | in-del | -/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985036 | TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCAC | 5521 |
rs34287861 | in-del | -/AT | 0.0437281 | 0.141251 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866646 | TATATATACACACAC[-/AT]ATATATGCACACAGA | 5521 |
rs34289574 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741050 | AAAAAAAAAAAAAAA[-/A]TGCAGATTTTTGGGT | 5521 |
rs34297187 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920799 | AGGGGAGTGGGTGGG[-/G]TACGTCTGCAGTATC | 5521 |
rs34317831 | snp | C/G | 0.00473736 | 0.048438 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638345 | AGCCGAGTTCCACCC[C/G]CATCATTGCAACACC | 5521 |
rs34318600 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895640 | TGATTTCTTTCCCCA[-/G]TTTATAAACAGTTGT | 5521 |
rs34324714 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737547 | GAAGAGCTGGGATTT[-/T]GAATCAGGTATGCCT | 5521 |
rs34349443 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948073 | AATTTAAAACTTGCC[-/C]ATGCTGTGTTCATAT | 5521 |
rs34352841 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894614 | CAGCTAATTTTTGTG[-/A]TTTTTAGTAGAAACG | 5521 |
rs34369345 | snp | A/G | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857876 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 5521 |
rs34377541 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785026 | AGAATAAAGTACAAT[C/T]GTAGCACTCCATTTT | 5521 |
rs34379716 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873118 | GTCTGTTTCCGCTTT[-/T]AGTGATGCGCCCCAT | 5521 |
rs34384078 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074360 | CCTGAAATGGGAATT[C/T]TTTTCATTGCCAGCC | 5521 |
rs34384290 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763189 | ATCCAAAGTGCTTTT[-/T]GCTCCACGACCTGCT | 5521 |
rs34390348 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876155 | CACATGCCAGAAATC[-/C]TCATTGCTATAAACT | 5521 |
rs34396932 | in-del | -/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601500 | TGGATGAGCTACTAT[-/T]GGGCCACTGCACCCC | 5521 |
rs34408776 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922326 | AAGCTCACCTTACCT[-/G]TTTTTATATCAGAAA | 5521 |
rs34409992 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590479 | TGGTGAGAACTCTCC[-/C]TTGTAATTTGCTTTT | 5521 |
rs34437765 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754405 | ATGAAGTTGACCCCC[-/C]ATGTATTGTCATGGA | 5521 |
rs34460257 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941731 | AATGAAGAGACTTTT[-/T]ATTGCATCTGTATAG | 5521 |
rs34480164 | in-del | -/TT | 0.375 | 0.216506 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072205 | ATCTAAACTAACTTT[-/TT]GTCTGCAATGTGGGA | 5521 |
rs34492498 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591728 | GAAATTAAACTTCCC[-/C]AGTTGTGATGTTATA | 5521 |
rs34494402 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862764 | AATTTTTTTTTTTTT[-/T]TGCCTTTTCAGCATG | 5521 |
rs34494552 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949569 | ATGCTGTTGGTGGGG[-/G]ATGTAAATTAGTACA | 5521 |
rs34508221 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665559 | TCAAACCTTCTCTAT[-/T]GTCAGCAAGAAGGTT | 5521 |
rs34512431 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863045 | TTGCTTTTTTTTTTT[-/T]CCACAGTGCACAGAG | 5521 |
rs34531502 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028549 | TGTAAGCTGTCCTTT[-/T]GTATAAATATCTCAC | 5521 |
rs34531884 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669355 | TCTTTCTTTAGACCA[A/G]TGGTCTGGGTGGATC | 5521 |
rs34538093 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680583 | GCGTTGCACACACTT[-/A]AAAAAAAAAAGTTCC | 5521 |
rs34538399 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736393 | ATGCATTTGCTCCTT[-/G]CAGTCATCACAGAAA | 5521 |
rs34550089 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999886 | GTAAAGGCCACAGGG[-/G]AAAGTCTTGAAACTT | 5521 |
rs34577647 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688739 | GGATGGAATTCTCCC[-/C]AGGGGTTAAGCACAG | 5521 |
rs34581719 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683192 | TCCTACCCCGCCTTT[-/T]CCCAAAATTAAACAG | 5521 |
rs34591087 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839415 | ATCCCAGCTACTCGG[A/G]AGGCTGGGGCAGGAG | 5521 |
rs34599029 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713588 | AGGGCTGAGGTAGAA[-/A]TTGGGAAGTGTATTG | 5521 |
rs34603081 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689365 | GGTTCCATAAGATTA[C/T]AATACTGTATTTGTA | 5521 |
rs34629120 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005832 | AGAGAGAAAGAGAAA[-/A]TAGTAAATAAAAAAC | 5521 |
rs34632167 | in-del | -/AC/ACACAC | 0.493635 | 0.150318 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915447 | CACACACACACACAC[-/AC/ACACAC]GTACACATGTGTGCA | 5521 |
rs34635154 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775948 | CTTGTACACTGAAAA[-/A]CTACAAAACATTGCT | 5521 |
rs34636688 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794819 | ATCATATTAATATGG[-/G]TGCAGTTTTATTTTA | 5521 |
rs34669885 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035675 | TCTGCCAAGGAGTTT[-/T]AGTTTGAAATAGGAG | 5521 |
rs34671926 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046277 | CCAAAAAGTGACATT[-/T]CTCGTGTATCAACAA | 5521 |
rs34684366 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028849 | ATTGATATTTTTAGT[-/G]CCTTTTAATTCTAGC | 5521 |
rs34693925 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029095 | TTTCTACACTGTGTC[-/C]TTGCCTTTTTAGTCT | 5521 |
rs34694594 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826909 | TTTACCTTGCTATCT[-/T]AACTTATATTAATTG | 5521 |
rs34698553 | in-del | -/TA | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866630 | ACATACATATATATA[-/TA]CACACACATATATAT | 5521 |
rs34704918 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988922 | GAAAAAGATGACATT[-/T]ATAACTGATGCCACA | 5521 |
rs34714820 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685176 | TTTAAATCAAGTGCC[A/G]TGCCATAAATAGTCC | 5521 |
rs34720742 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076585 | TAAACATTATGTTTT[A/T]AAAAATTATTTAAGG | 5521 |
rs34722016 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057409 | TGCAGGAGTGTCTCC[-/C]TAAGAGATACTTCAT | 5521 |
rs34725004 | in-del | -/A/AA | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619322 | AAAAAAAAAAAAAAA[-/A/AA]TACAAACATTAGCTG | 5521 |
rs34726231 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744607 | TCCATCAGCACTGGG[-/G]ATATGAGCCAGGCAA | 5521 |
rs34733993 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839401 | GCATGTGCCTGTAAT[-/A]CCCAGCTACTCGGGA | 5521 |
rs34745136 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903167 | TAATTTTTCATAAAA[A/G]CATGCCATTGATGTT | 5521 |
rs34746460 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951993 | TTTTTTTTTTTTTTT[-/T]AAAGCTCCTCAGTGA | 5521 |
rs34748772 | in-del | -/AT | 0.306431 | 0.243548 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915480 | CACACACACGTACAC[-/AT]GTGTGCAATTTACAT | 5521 |
rs34771839 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681606 | TTTTCACTTCCTTTG[-/G]AAAAGTATACAGAGA | 5521 |
rs34776190 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030678 | AATTGCAACATACAT[-/G]CTATTAATTATTAAA | 5521 |
rs34780019 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864422 | AAAAAAAAAAAAAAA[-/A]GCACAGCTTTCCGAA | 5521 |
rs34787816 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796373 | GTGCAATGCACTTTT[-/T]ACCAAGTGATAAGTT | 5521 |
rs34793084 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021202 | ACTGTAACCACCTAG[-/C]AAAAGGAAAACAAAC | 5521 |
rs34793560 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827675 | AAGGAAATTTCTCCC[-/C]ATTCATTTATATAAT | 5521 |
rs34806760 | in-del | -/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592420 | ATCAGAGAATCATTT[-/T]GTATTTGTCAAACTA | 5521 |
rs34810946 | in-del | -/GTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973077 | ATGATCTTTAAAAAT[-/GTT]CTGTGGTATCCTTTT | 5521 |
rs34829156 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819669 | TGAATTTGCTTTTTT[-/T]AAAGAAATTACAGAG | 5521 |
rs34830622 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022412 | ATAAAAAAAAAAAAA[-/A]TTGTTGGGTGTGGTA | 5521 |
rs34835501 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926915 | GCTGATGGCCCTCCC[-/C]AACTCACTCCCATCC | 5521 |
rs34843734 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039064 | TTCCAGCCTTTGTCC[-/C]AGTCCTCTGTGCTTG | 5521 |
rs34854961 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995459 | TGCCTTATAAGAACT[-/G]ATTCTCTATGGCTGA | 5521 |
rs34857954 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074342 | AAGACAGGATTCCTT[C/T]TGCCTGAAATGGGAA | 5521 |
rs34864782 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979598 | CACACACACACACAC[-/AC]GCTAGTCCCTCTTTA | 5521 |
rs34880093 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798601 | TACCAATGATAAAAT[-/G]CAACACCTAACATAA | 5521 |
rs34883893 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890641 | GGTTGTATATATTTT[-/T]AAAACTCAATAAATA | 5521 |
rs34886911 | in-del | -/A | 0.352504 | 0.228019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821778 | GCCTAGTACTCTGCC[-/A]AAAAAAAAAAAGCTT | 5521 |
rs34887581 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823449 | TGATCTGCCCTCCTC[A/G]GCCTCTCAAATTGCT | 5521 |
rs34890768 | in-del | -/CGCGCA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667329 | AGGAATAGGCGTGCG[-/CGCGCA]CACACACACACACAC | 5521 |
rs34893993 | in-del | -/AC/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050673 | GGGATAAACACACAC[-/AC/CA]ACACACACACGCATC | 5521 |
rs34896382 | in-del | -/A | 0.478437 | 0.10157 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977049 | AATCCCAAACAAAAC[-/A]AAAAAAACAAATCTG | 5521 |
rs34902638 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907479 | GAAAGTGGAATTAAT[A/G]TCCTTACAGAAGGGC | 5521 |
rs34921271 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880164 | GAGCAGAAATGTTCC[-/C]TTGACATAGTTATTT | 5521 |
rs34933173 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843809 | GCTGCATAGTATTCC[-/C]ATGGTGTATATGTGC | 5521 |
rs34954272 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852672 | CTCTCCAAACATTCT[C/G]AACAATTCCCAATGA | 5521 |
rs34956237 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633604 | TAGCAGGCTGGCAGC[-/C]TTGCAATTCAGAACT | 5521 |
rs34960008 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677525 | CTTTTTAAAAAACTC[A/C]TCCCTCCCTCCCTCC | 5521 |
rs34969922 | in-del | -/A/AAA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027651 | AAAAAAAAAAAAAAA[-/A/AAA]TTTAGTGTGGATGGC | 5521 |
rs34971472 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740893 | CACAATCACCAAAGG[-/G]AACACATTAAAAATG | 5521 |
rs34973819 | in-del | -/A | 0.476487 | 0.105846 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991693 | CAACTTGTACTCCCT[-/A]AATATGTACAATTAT | 5521 |
rs34975709 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831499 | AAAAAAAAAAAAAAA[-/A]GCCTCTGGGTTGATA | 5521 |
rs34981622 | snp | A/G | 0.328148 | 0.237472 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703798 | GGAGTATTAGGCATG[A/G]TCCCAGGTAATACAA | 5521 |
rs34985894 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066948 | GCTACTGTCTTTCCT[-/G]CCTTTAATATTTGTG | 5521 |
rs34989073 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810364 | TTTCCCGTTATAAAA[-/A]CCATCAGATTGCGTG | 5521 |
rs35003679 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886825 | ATTTTAAACTTTTTT[A/G]GTAAAAAAAAAAAAT | 5521 |
rs35011506 | in-del | -/A | 0.0370239 | 0.130924 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040809 | AAGATGAGTTTCCTT[-/A]AAAAAAAAAAAAAAA | 5521 |
rs35015788 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859157 | AGGTATGTGATCATA[A/G]ACAAGTTGATTAACT | 5521 |
rs35023590 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808959 | CAGCTGCTAACACTG[-/GT]GTGTGTGTGTGTGTG | 5521 |
rs35030906 | in-del | -/GA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827966 | TGCCTTGCTCAGGGG[-/GA]AAAAAGAATTGGGAG | 5521 |
rs35038153 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707391 | TTCAGGTTAAGGGGG[-/G]TTCAGCAGGCTCTGG | 5521 |
rs35052703 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833540 | TTCAATGTGACAAGG[-/G]CAGTGTCTAACTTCA | 5521 |
rs35054666 | in-del | -/T/TT | 0.495483 | 0.0473088 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768888 | AAGATTTGTTGTTAC[-/T/TT]TTTTTTTTTTTTTTG | 5521 |
rs35055298 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934772 | AACTCTTTTTTTTTT[-/T]GATTGAAAGGTGTTG | 5521 |
rs35059381 | in-del | -/T | | | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081394 | TGAACTGGAGCAATT[-/T]GGAGTTTGTCCCTTC | 5521 |
rs35064496 | snp | G/T | | | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766435 | ATGCCTAAGCCAGGA[G/T]TGAGTGGGGAGTGGG | 5521 |
rs35065666 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950171 | GGAGATGGGCACCCC[-/C]ATTTATCCCGATGTG | 5521 |
rs35072756 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702112 | GGCCTTTGACAGGAA[-/A]CATTCTGAAGATAAT | 5521 |
rs35073767 | snp | C/T | 0.247621 | 0.249989 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685103 | TAGCATAGTAGACAC[C/T]GAGATACAAAATACA | 5521 |
rs35076487 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038967 | ATTATTGATTTTTTT[-/T]AAACACAACTGCAAC | 5521 |
rs35087951 | in-del | -/AGAG | 0.489665 | 0.0711382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828000 | CCATGGCCTAGTTGA[-/AGAG]AGAGAGAGAGAGAGA | 5521 |
rs35102051 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658825 | CGCATAGACGCCCCC[-/C]ATCCCCAGATCATTA | 5521 |
rs35106084 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626639 | CTTTGCTAGTGATAG[-/G]CTTGTTACAGGGCAT | 5521 |
rs35116651 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677260 | ATAGTCAGTGTCCTT[-/T]ATTTAATTGAATGTT | 5521 |
rs35127306 | in-del | -/A/AAAAA | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912261 | AAAAAAAAAAAAAAA[-/A/AAAAA]GTTCCCTAAGAGAGG | 5521 |
rs35128018 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691113 | GTGGTGGCCAGGGCA[C/G]CTGTTTGCACTCACC | 5521 |
rs35131166 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650540 | CTTGATCACAAAGAA[-/A]GGATACTAAAACTTT | 5521 |
rs35134658 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956413 | CCCTGGTCACTCCCC[-/C]AGAAAGCTTGCTCAA | 5521 |
rs35190605 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019946 | TAGCATGGGTACTAG[-/G]ATCTGGCCATTCCTT | 5521 |
rs35203174 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936472 | GAAAAAAAAAAAAAA[-/A]CCCTAGACAGTTATG | 5521 |
rs35204549 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658117 | TCAAACCACCCCTTT[-/T]GGGAAGGCTGTTTGA | 5521 |
rs35208166 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062086 | TATGAAGGTGTCCCC[-/C]GTAAGATTATAATAC | 5521 |
rs35212537 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742086 | ACGTTCTTACAAAGG[-/G]AAAATGTTATGTATG | 5521 |
rs35217325 | in-del | -/ATTT/ATTTATTT | 0.326035 | 0.238157 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906306 | TTTATTTATTTATTT[-/ATTT/ATTTATTT]GGAGACAGAGTTTCA | 5521 |
rs35252210 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905890 | TTTTGGGGATGATGG[-/G]AAATGTTCTCTGTGC | 5521 |
rs35254445 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031087 | AAAAAATGCAAAAAA[-/A]TTAGCTGGGCATGGT | 5521 |
rs35261868 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000337 | ACCCTCTAAGGGCTC[-/C]TTCAAGTTTGAACTT | 5521 |
rs35263636 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080953 | AATGCAATTTTGGGG[-/G]TGTGTGGGGACTTAG | 5521 |
rs35264820 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812911 | GGGAAAACCACCCCC[-/C]ATGATTCAGTTATAT | 5521 |
rs35269606 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987962 | ACCAAAGAGGGCAGG[-/G]AGTAGCTATACTTAT | 5521 |
rs35292569 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075344 | GGCATCCTAACCACC[-/C]AGCATAACAGTGTAA | 5521 |
rs35309411 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780693 | ATCACTAGGAATCCC[-/C]TGTGCTGTTTGCTGT | 5521 |
rs35311964 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941509 | ATGATGCTTCTGTTG[-/T]CTTAGGGGTGTGTTC | 5521 |
rs35321883 | in-del | -/CACA/CACAC/CACATA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009899 | ACACACACACACACA[-/CACA/CACAC/CACATA]TATATATATAGGACC | 5521 |
rs35327338 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941511 | TGATGCTTCTGTTGC[-/T]TAGGGGTGTGTTCAG | 5521 |
rs35327477 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803116 | AAACATGTTTATTCC[-/C]ATAGAGCGCATGCCT | 5521 |
rs35337541 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848579 | CCACAGAGATAAAGT[A/G]CCATTTCCATCCTAT | 5521 |
rs35338102 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863045 | TGCTTTTTTTTTTTT[-/T]CCACAGTGCACAGAG | 5521 |
rs35357763 | in-del | -/A | 0.133777 | 0.221342 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737957 | AAAACAAAACAAAAC[-/A]AAAAAAACGTTGTTA | 5521 |
rs35358102 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847027 | GGGAAAACATCTTCA[C/T]ATAATTTTAGAATCA | 5521 |
rs35362130 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776817 | AAAGACAAACAACCC[-/C]AAATAAAAAATGGGC | 5521 |
rs35372337 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773387 | GCTTGCACAAAGCAG[-/C]AGCCAGGCTTCATGC | 5521 |
rs35373015 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921900 | ATGTGCAAGTCACTT[-/G]GGATGAGTGCTTTAA | 5521 |
rs35379341 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062899 | GAAAGTTTGCTATTC[-/C]TAGGACATGGTGCCA | 5521 |
rs35383221 | in-del | -/T | 0.481703 | 0.0938806 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993808 | AAATATCCAGCACAG[-/T]TTTTTTTTTTAAATA | 5521 |
rs35394182 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770909 | AACCTATTTACTTTC[-/C]TCAAAAGAAAACAAA | 5521 |
rs35394507 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626018 | GGAAACATTCCCCCC[-/C]TAGAGCCTCTAGCAG | 5521 |
rs35400648 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650540 | TTGATCACAAAGAAA[-/A]GGATACTAAAACTTT | 5521 |
rs35421976 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732728 | GAAGAGGAATACTAC[-/C]TAAGTAACAAGTATT | 5521 |
rs35433244 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761552 | AGCACACCAACATGG[-/G]CACATGTATACATAT | 5521 |
rs35441821 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873110 | GTTTTCAGTCTGTTT[-/T]CCGCTTTTAGTGATG | 5521 |
rs35449817 | in-del | -/AA | 0.318896 | 0.240319 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919968 | TGTGTAACTTTTGAT[-/AA]GTTACTTAATATCTT | 5521 |
rs35452445 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982889 | TGTATATCTTTTTCC[-/C]ATCCTTTTACTTTAA | 5521 |
rs35458270 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664705 | TGGTGAGTGCGTCCC[-/C]AGAAGATGTTCAATT | 5521 |
rs35465313 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049879 | TGACAGTGAGTGTGG[-/G]ATGACACTTTCAAGG | 5521 |
rs35472545 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005165 | ATGACTGCCAACAAA[-/A]TTATAGTCCAGACTC | 5521 |
rs35480745 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691112 | TGTGGTGGCCAGGGC[-/A]GCTGTTTGCACTCAC | 5521 |
rs35501029 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772689 | CACCACCATAGAAGG[-/C]ATGAACAATGTGTCC | 5521 |
rs35502873 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995662 | TCTTTTGATGACTTA[A/G]AAGAAAATTCTATGC | 5521 |
rs35505663 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774471 | AAATAAAGTGGGGGG[-/G]TTGTATACTAACATT | 5521 |
rs35515872 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077310 | CACACACACACACAC[-/A]CCACACCCACACCCC | 5521 |
rs35533710 | in-del | -/TA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698351 | ATATATATATATATA[-/TA]CACACACATATAATT | 5521 |
rs35564080 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666824 | TTTCTGTATGTTAAA[-/A]CAGACTTCCCTTTGT | 5521 |
rs35573618 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826148 | TTGGCATTTCTTTTT[-/T]AAAAATGCCCCAGTC | 5521 |
rs35577600 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684336 | GCTGATCCTGACTCA[A/C]CCAATAATTTGCACT | 5521 |
rs35591095 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963689 | AATGTTATTATCCCC[-/C]ATTTTAAGAAGTCTG | 5521 |
rs35601188 | in-del | -/A | 0.499968 | 0.00399348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078827 | AAAAAAAAAAAAAAA[-/A]TTGTATCACCCTGAC | 5521 |
rs35622605 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079445 | CATTTTATATATATA[C/T]ATATATATATATATA | 5521 |
rs35623861 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963462 | CTCCTACCTGAACTT[-/G]CCAGGTTAGTCCTCC | 5521 |
rs35647125 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061548 | GGGTATGTTGTCTTT[-/T]CTCGCTCATTGCATC | 5521 |
rs35660523 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818593 | GCACCTTACCATGTG[-/G]CGGGTTCTATCCCCT | 5521 |
rs35662816 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891749 | AAATGTAGAGGCATC[-/C]TAGTGGAATGAGAAT | 5521 |
rs35664603 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075243 | CCTGCTAAGCAAATC[-/C]AAATACAAGCATTGC | 5521 |
rs35707966 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894619 | AATTTTTGTGATTTT[-/T]AGTAGAAACGGGGTC | 5521 |
rs35718500 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914573 | CTTTTAAAAGCACTT[-/T]AAAATCTGGGAACCA | 5521 |
rs35727657 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926554 | GATTTTATTTTTAAA[-/A]CTTGGCTTGCTAGAG | 5521 |
rs35732225 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626515 | AGGCCAGTGCCCTCC[C/T]TAGGCTCTAACAGGC | 5521 |
rs35734395 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827208 | GCTGAATTGCCAGGG[-/G]AATTAGGAGAAATTT | 5521 |
rs35736976 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641705 | AAACCCAGGCATTTT[-/C]CCCCTGCACAACTCT | 5521 |
rs35741023 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793413 | ATATAGATACTATTT[-/T]CAAGTCACAAGAGTA | 5521 |
rs35752834 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016306 | CACCACTGCACTCCT[G/T]CCTAGGTGACACAGT | 5521 |
rs35755206 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022558 | AGCAAGGCTCCATCC[-/A]AAAAAAAAAATCCAA | 5521 |
rs35783219 | in-del | -/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605676 | AATGTTCCCCAGGGG[-/G]CATGACTGCCCCTGG | 5521 |
rs35792034 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837955 | GGCATGTTTGTTCCC[-/C]TAGCACCATGACCTA | 5521 |
rs35817303 | in-del | -/AC | 0.486266 | 0.0817214 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053226 | CATTAAAAAAAAAAA[-/AC]ACACGCGCACACAAA | 5521 |
rs35829196 | snp | C/T | 0.284733 | 0.247575 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781472 | TGGATATTTAGTTTA[C/T]GTTAACACAAAAATC | 5521 |
rs35834180 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803150 | CCATCCACACCTAAA[-/A]TGCTTTACAGCTACT | 5521 |
rs35851790 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732757 | TTGAGTACTTTGTGT[-/T]CAAGTGCTCAGCTAC | 5521 |
rs35857989 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705301 | GGTTTTGGTAGTTTT[-/T]CGCCTTCAGCTAAGA | 5521 |
rs35859017 | in-del | -/G | 0.416545 | 0.186448 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657684 | TAAACACTTCTGAGA[-/G]GGGACATTTGCATGA | 5521 |
rs35863564 | in-del | -/AAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027635 | CGAGACTCGGTCTCA[-/AAA]AAAAAAAAAAAAAAA | 5521 |
rs35885710 | in-del | -/AC/CA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972210 | ATTAGAATGGGGTTA[-/AC/CA]GTTTTTGGAAGGAAC | 5521 |
rs35885867 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037086 | CAGTAGAGCACAGGG[-/G]AACCCAGGCAGTCTA | 5521 |
rs35891757 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922269 | TTTCTTCCAAGTGTG[-/G]CATGATATCAAGGAT | 5521 |
rs35892639 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850998 | TTGGTCACCCCAAGG[-/G]ATGAGTAAATAAACA | 5521 |
rs35893043 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018018 | CAGATGAATTATAGT[C/G]TACGACACACACATG | 5521 |
rs35893109 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825729 | AAGCCACTAACTTTT[-/T]GGAAGTGCTGTAGTT | 5521 |
rs35926273 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906720 | CTTTCTTCTACTTTT[-/T]GGAAATGTGGCCACT | 5521 |
rs35933293 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755760 | TTGGATTTCTTTTAG[-/G]CTTGTGCTAATTTGT | 5521 |
rs35936080 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675449 | AGCAGGTTAGTTGCA[-/C]ATTGGTCTGTCTCAG | 5521 |
rs35949206 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691578 | TACAATGTAACTAAG[-/C]AATTTTACATGAAAA | 5521 |
rs35959894 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638743 | AATGTACCAAGTTGC[-/C]AAAGATTTTGCTTCT | 5521 |
rs35965732 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772336 | TATGAGCACGTAGAA[-/A]TGTATATTTTAACAT | 5521 |
rs35968138 | in-del | -/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605797 | CAGCTCAGTGTTTTT[-/T]CTAGTACAGGCTTCC | 5521 |
rs35979783 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728871 | AAGTCCAATTAAACC[C/T]CTTTTTATTTCCAGT | 5521 |
rs35993968 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660036 | ATTAACTTTATTGAG[-/G]AATTTAAAAAGCTGA | 5521 |
rs35997649 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909192 | TGAGGAATTAAGAGA[-/A]CTAACTAGGGGTTCC | 5521 |
rs35999961 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807924 | CTGCCTCAGCCTCCC[-/C]AAGTAGGTGAGATTA | 5521 |
rs36002908 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698438 | TTAAAATAGAACAAA[A/T]TTTTAAAATCAATAT | 5521 |
rs36020514 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015528 | CCATCTCCTTCATGG[-/G]AGCCTTCTCTGATTC | 5521 |
rs36025341 | snp | C/T | 0.444444 | 0.157135 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706895 | AGCACCACAGACGTG[C/T]CCGAGATCTGGGACT | 5521 |
rs36060530 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877846 | AGCCCGGATGGATGC[-/T]GAGGTGCACTGGGGC | 5521 |
rs36073833 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809966 | GGAGTACAAAAAAGG[-/C]ACTTGCTAGCCAATC | 5521 |
rs36086598 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029263 | TATGTTATAGTCTAG[-/C]AAAGTTTAGTGTTTT | 5521 |
rs36087089 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027990 | CGGACTTTGTGGCTT[C/T]TGTCTGTACTTCAGG | 5521 |
rs36091709 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843263 | GATTACATCTTTTTT[-/T]CAGTATCTAATGACA | 5521 |
rs36096827 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619491 | AAACAAAACAAAACC[-/C]ATAAAGGGGCAATTT | 5521 |
rs36114538 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917141 | ACAATCTCTTCCTTT[-/T]GAGTCTATTTGCTGA | 5521 |
rs36115009 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076596 | TTTTAAAAATTATTT[-/T]AAGGTTTGTCTTAAA | 5521 |
rs36115021 | snp | C/G | 0.188 | 0.24219 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762185 | AAGAAAAAAGTTACT[C/G]ATATTGGCTAAAACA | 5521 |
rs36147691 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017978 | AGGACCATGTAGTTT[-/G]TGCATGTAGGAAATC | 5521 |
rs36211249 | in-del | -/CACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740618 | ACACACACACACACA[-/CACACA]GATAAAAGTTCTTGA | 5521 |
rs36219835 | in-del | -/ACACACACAC | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865294 | CTCTCTTTGTCTCTG[-/ACACACACAC]ACACACACACACACA | 5521 |
rs41418045 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666491 | CTCTTCTTGGGAAAA[C/T]TTAAGCATCTTTAAT | 5521 |
rs55634661 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743694 | CTTCCTGTCAAGTTT[A/G]TTTTCCCCAAGCTTC | 5521 |
rs55656252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981276 | TCCCTCTTTTAGGGA[A/G]AGTCTTGGGTGGTAA | 5521 |
rs55669605 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818729 | AAGATGATAGAGGAA[A/G]TAATGGTAGGGATTT | 5521 |
rs55675734 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007272 | CAGCAGTTGGGGTGT[C/T]CTGTTTAGAGGGGGG | 5521 |
rs55680436 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668790 | CAAGTTTTCAAGGTT[A/G]TCATCCATTTCTGTA | 5521 |
rs55681529 | in-del | -/A | 0.493401 | 0.0570604 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035800 | ATGAAAACTGAAGGG[-/A]AAAAAAAACAGTTTG | 5521 |
rs55681635 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933565 | CCACCTCACTTTATT[C/T]TGAAATTTCTACTTC | 5521 |
rs55691204 | snp | A/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862245 | TGGCTGCTCTCCTAA[A/C]TACAGAAATGCTGTT | 5521 |
rs55694055 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952396 | AGTGAGGCTGTCAAT[C/T]AGGATGCCTTGAATG | 5521 |
rs55719630 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895929 | GTCACAGACCAGTCC[A/G]TGATTCTTCAATAAG | 5521 |
rs55719903 | in-del | -/AC | | | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767020 | ACCACACCATTGCAC[-/AC]TCCAGCCTGGGCATA | 5521 |
rs55824663 | snp | C/T | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911114 | TTTGAGATGGAGTCT[C/T]GTTTTGTCCCCCAAG | 5521 |
rs55841193 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619588 | AGGCCTAAATTTTTT[A/G]AGGAACTCTAATTTT | 5521 |
rs55860458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618813 | TCAGAGAAACCAGAA[A/C]CCAGCGGCTGCAAAG | 5521 |
rs55877177 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969917 | TCCACGAAGCAGTTG[A/G]ATTTATGTCTGAAGC | 5521 |
rs55879140 | snp | C/G | 0.115438 | 0.210697 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843844 | TTTTCTTAATCCAGT[C/G]TATCATTGTTGGACA | 5521 |
rs55884249 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819688 | GAAATTACAGAGATA[C/T]CCTTAAAAACATGCT | 5521 |
rs55898541 | in-del | -/T | 0.0962929 | 0.197165 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907209 | ATTGGCTAAATTACA[-/T]TTTTTTTTTCCATCA | 5521 |
rs55922905 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693870 | GACAGCTTTAGCTTC[A/C]ACCCTCAATGATGTC | 5521 |
rs55925964 | snp | A/G | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912013 | GAGGCTGAGGCGGGC[A/G]GATTGCCTGAGCTCA | 5521 |
rs55952919 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969916 | ATCCACGAAGCAGTT[G/T]AATTTATGTCTGAAG | 5521 |
rs56007229 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040838 | AACTGTAAAATAATA[A/G]TGCCATTACACATAC | 5521 |
rs56046133 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072056 | AGGGGAAGATGAGCA[C/G]TAAAAAAATTTCTGG | 5521 |
rs56066932 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706058 | GGGCGGGGGTCCCCA[A/G]GCAGTGAACTCCCCC | 5521 |
rs56070805 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877893 | GCCCCCGCCCCAGCC[C/T]TAGGGCCCGGAGGAG | 5521 |
rs56122336 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692124 | CTTGTTTATCACTGT[A/G]CCACCAGCACCCAGA | 5521 |
rs56133580 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912263 | AAAAAAAAAAAAAAG[G/T]TCCCTAAGAGAGGTA | 5521 |
rs56140835 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765248 | ATGATATCTGAATGC[C/T]TTCACATCCCTTAGC | 5521 |
rs56182789 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809644 | TAAGCAAGGAGTGGG[C/T]CACGAGGCTGTGGGC | 5521 |
rs56185110 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995613 | CACAAGTTCAACTCC[A/T]TATTTCCTGCATTGC | 5521 |
rs56191449 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810866 | CTCCTAATGCTATCC[C/G]TCCCCCCTCCCCCCA | 5521 |
rs56236653 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590266 | TGACATATCTTCACT[C/G]TCTTTTCTTTTTGGA | 5521 |
rs56241843 | snp | C/G | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911362 | GCTAGGATTACAGGG[C/G]TAAGCCACGGTGGCC | 5521 |
rs56262787 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707352 | CTTCTCCTGGGTGCA[C/T]ACAGCATGGATGTTG | 5521 |
rs56265054 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819593 | TCTAGCTTTGGAATA[C/G]TTATCGTTTCCTCCA | 5521 |
rs56268466 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740630 | ACACACACAGATAAA[A/T]GTTCTTGATGGATGC | 5521 |
rs56361052 | snp | A/C | 0.391583 | 0.206044 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692888 | TCATGTCTGCTGGCC[A/C]CATGCTTTGGTGGGC | 5521 |
rs56371061 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849105 | ATACTTCCTTTGCTA[C/T]TAGTAGCATCAGACA | 5521 |
rs56376596 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951451 | GCACCTATCAACCCA[C/T]CACCTAAGTATTAAG | 5521 |
rs56403847 | snp | A/T | | | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650584 | AAAGTTCCATAGGTT[A/T]ATCCTCAGGTCATCA | 5521 |
rs56672131 | snp | G/T | 0.33875 | 0.233717 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964998 | TAACTTTCCTTCCAA[G/T]TCTAGCATACCATCA | 5521 |
rs56677078 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925759 | TTCTCTCCTTCCGAC[A/C]TTCCCCTGACATGGT | 5521 |
rs56685778 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697628 | TATGCCAACCTCACA[A/G]AGACAGCATGTTGAG | 5521 |
rs56686117 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830530 | GCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 5521 |
rs56697862 | in-del | -/TATATATATATATATA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781161 | ATATATATATATATA[-/TATATATATATATATA]AAATTATTCTCATGA | 5521 |
rs56705990 | in-del | -/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828262 | CTTTTACTTTTTTTA[-/TT]AAAAAAAAAAAGACA | 5521 |
rs56730491 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015261 | CGTCTCATATCATTG[A/C]CCTGTTTTAAAATTC | 5521 |
rs56752268 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962080 | GTTAATAAACTCTTC[C/G]CAACATCCCTGCCCC | 5521 |
rs56757250 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992506 | AGTGACTCTATGTTG[C/T]GGGGAGGGCTTGTTT | 5521 |
rs56791426 | snp | A/G | 0.2776 | 0.248472 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608012 | CACTATTCTTTTTTG[A/G]TTTCTTCAACTATTT | 5521 |
rs56805672 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050689 | ACACACACACACACA[C/T]GCATCCATACCTACA | 5521 |
rs56866551 | in-del | -/CAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686626 | AATTGTATTCATCAC[-/CAC]ATCACCTTCATTTTG | 5521 |
rs56893200 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745208 | AGAGAGAGAGAGAGA[A/G]AGAGACTATAAGCAT | 5521 |
rs56958399 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716774 | AAACCAAGTAAGGAC[A/T]GTTTACATTTAAAAC | 5521 |
rs56989825 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697724 | ACACCTGCAAATAAT[C/T]TGCAATAGTTGAAAA | 5521 |
rs57014772 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740422 | GCTTTGAAACCACCA[C/T]GGGAAGAGGCTGTTG | 5521 |
rs57076058 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749699 | CGCCTCCCAGGTTCA[C/T]GCCATTGTCCTGCCT | 5521 |
rs57080635 | in-del | -/TATC/TATCTATC | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024203 | ATCTATCTATCTATC[-/TATC/TATCTATC]ACCTACTGGTTCTGT | 5521 |
rs57092441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792529 | CAAACAATAAATAAG[G/T]AAGGTATGTAGTATG | 5521 |
rs57101353 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068682 | GCTTTACATGAATCA[A/T]TGACTGAAGAAAGAA | 5521 |
rs57146550 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724010 | GATGTTATCTTATTT[C/T]CAATTTTTATATTTA | 5521 |
rs57151657 | in-del | -/TGTG | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880222 | GTGTGTGTGTGTGTG[-/TGTG]GTGGGGGGAGTTCAG | 5521 |
rs57183678 | in-del | -/G | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638035 | ACCCTTTTCTGATGA[-/G]GGTCATGTCTTATTT | 5521 |
rs57213493 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779827 | CCTCCCTCCCTTCTG[C/T]TCAGTTTAATGCCTG | 5521 |
rs57228238 | snp | A/T | 0.406296 | 0.19512 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991062 | TATCATTAAAAAGAT[A/T]AAAAAAACACAAATG | 5521 |
rs57285530 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698359 | ATATATATACACACA[-/CA]TATAATTATACACAT | 5521 |
rs57335797 | snp | A/C | 0.361894 | 0.223562 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681263 | AAAAGGGATCTAGGC[A/C]TGTATTTTTGATCTT | 5521 |
rs57339201 | snp | C/T | 0.282632 | 0.247861 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619911 | CCTTCTAATCTTCCT[C/T]CTATTATTTTTAAAT | 5521 |
rs57408722 | in-del | -/TGCTGCTGCTGCTGCTGCTGC | | | intron-variant, utr-variant-5-prime, cds-indel, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878759 | TGCTGCTGCTGCTGC[-/TGCTGCTGCTGCTGCTGCTGC]AGGAGGCTGGAGGCG | 5521 |
rs57417705 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640414 | TGCTGTGGAGCAAGA[A/G]CCTGTGCCCCTCAGG | 5521 |
rs57455873 | in-del | -/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903339 | GTTTAAGAAACACTG[-/T]TTTTTTTGTTTTTGT | 5521 |
rs57518534 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616459 | TAGGATGAGGGAAAA[C/T]ATTTGCAAACTACCC | 5521 |
rs57537297 | in-del | -/AACT | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750092 | AAAAACAAACAAACA[-/AACT]GAGTTGAACATATTT | 5521 |
rs57577845 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681040 | ATTTTTCTCTGGTAA[A/G]GACTGGTATTTAAAA | 5521 |
rs57616192 | snp | A/G | 0.377385 | 0.215112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663768 | GACTCAATGTTGATG[A/G]ATGCTGATTGATCAG | 5521 |
rs57617905 | snp | C/T | 0.103082 | 0.202275 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993400 | GGCTGCTCTACCACA[C/T]CTGACTAATTTTTGT | 5521 |
rs57629536 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936529 | CAAAAAAAAAAAAAA[A/G]AAAAAACAAGACATG | 5521 |
rs57666120 | snp | A/G | 0.0423829 | 0.139266 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777620 | AATGGTAAATTTTAT[A/G]TTATATATATTTTAC | 5521 |
rs57781048 | in-del | -/TGTGTG | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880220 | GTGTGTGTGTGTGTG[-/TGTGTG]GTGGGGGGAGTTCAG | 5521 |
rs57882196 | in-del | -/ACACAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634778 | TACACACACACACAC[-/ACACAC]CCCCTACTGGTTCTG | 5521 |
rs57891364 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870557 | GAGAAAACAAAATTT[C/T]TGTTATTTAGGCAAC | 5521 |
rs57912544 | snp | C/T | 0.32627 | 0.238082 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736486 | GATAACTAACTTGCT[C/T]CAGATCGTGCAGGAA | 5521 |
rs58108762 | snp | A/G | 0.440609 | 0.161766 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708924 | TCCTGATTCAGTAGC[A/G]TTACCTTCTTAACTT | 5521 |
rs58117040 | snp | A/G | 0.209084 | 0.246629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683186 | TACCCTTCCTACCCC[A/G]CCTTTTCCCAAAATT | 5521 |
rs58163975 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677933 | GTATGGAATCCTTTT[G/T]AAATAAGTGGCAGGT | 5521 |
rs58178462 | snp | A/G | 0.0271762 | 0.113356 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621153 | CTTCACTGTCTTCTC[A/G]TGGATCAGGCAGTCT | 5521 |
rs58202603 | snp | A/T | 0.261056 | 0.249755 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687375 | CATGATCTTGGGTAT[A/T]CTACTTAACTGCTTG | 5521 |
rs58227500 | snp | A/G | 0.297382 | 0.245469 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750005 | ATTTTGTGCCTATGG[A/G]AGTTCAATTGCACCA | 5521 |
rs58274851 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835947 | ATTTAAGCTATGGGA[C/T]CAATTATGAAACTTT | 5521 |
rs58353517 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726375 | ACTTTTTGGCTCTAG[C/T]GAGTTTATAGTCTCA | 5521 |
rs58355233 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664662 | TCCTTCCTTAAATCA[A/T]GAATGTTCTTAATGG | 5521 |
rs58393815 | in-del | -/TA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079469 | ATATATATATATATA[-/TA]CATGTGCAATGGAAT | 5521 |
rs58437325 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022003 | CCTAAAGGAACTTCC[A/G]GAGTTAAAAAATACA | 5521 |
rs58453914 | in-del | -/TATAT/TATATATA/TATATATATATA | 0.625 | 0.125 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781176 | ATATATATATATATA[-/TATAT/TATATATA/TATATATATATA]AAATTATTCTCATGA | 5521 |
rs58467095 | snp | C/T | 0.227959 | 0.249026 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844020 | AGATCCCTGAGGAAT[C/T]GCCACACTGACTTCC | 5521 |
rs58474398 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727777 | CACCAAGTTGTGCAG[A/C]TCTCTAAAACTTCTT | 5521 |
rs58481044 | in-del | -/AAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742650 | ATAATAAATGATAAT[-/AAT]TATTATGGGTTGAAT | 5521 |
rs58481127 | in-del | -/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673493 | GAAGATTTTTTTTTT[-/TT]ATTGCTACTAGAAAA | 5521 |
rs58493888 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866448 | GCAAAGTAGAAATCT[A/G]TTTTCTCTTTCACTC | 5521 |
rs58516893 | in-del | -/TATT/TATTTATT | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670513 | ATTTATTTATTTATT[-/TATT/TATTTATT]GAGACAGAATCTTGC | 5521 |
rs58520448 | in-del | -/GTC/GTCTT/GTCTTTT | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911090 | GTTAGACACTTTCTT[-/GTC/GTCTT/GTCTTTT]TTTTTTTTTTTGAGA | 5521 |
rs58520511 | in-del | -/AAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738415 | AAAAAAAAAAAAAAA[-/AAA]TCTTAGCTTCACAGA | 5521 |
rs58563475 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794322 | TAACCTTGAACTTTG[C/G]AGAGCAAATGGTAGG | 5521 |
rs58569193 | in-del | -/G | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880736 | TTGTAACCAATGGGG[-/G]AGAATGTCCCTTCCA | 5521 |
rs58571441 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948583 | GTAGAAAACAAAGGG[-/A]AAAAAAGAAATAACT | 5521 |
rs58583365 | in-del | -/ACAC | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915470 | CACACACACACACAC[-/ACAC]GTACACATGTGTGCA | 5521 |
rs58613574 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030178 | CTTTCTGCTAATAAA[G/T]TTTTTTGGTATTGAT | 5521 |
rs58634387 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644260 | AAAAAAAAAAAAAAA[-/A]AAAGAAGAAGAAAGA | 5521 |
rs58671380 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778541 | TTTTTCATCCTAGGG[A/G]CTGTGTCTTATTCAT | 5521 |
rs58702684 | snp | A/G | 0.141258 | 0.225111 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764052 | TATAATTATTAAAAG[A/G]AATTTCACAGAAAAG | 5521 |
rs58777308 | in-del | -/TTT | 0.491368 | 0.0651254 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903410 | TTTTTTTTTTTTTTT[-/TTT]AGAGACAGAATTTCA | 5521 |
rs58786812 | snp | C/T | 0.175576 | 0.238665 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683564 | CTTGGAACATTAGCA[C/T]AAATGTTAGCTTCTC | 5521 |
rs58843058 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870385 | TGCAAGAAGAAAAAA[A/T]AATGCCAGAGATTGC | 5521 |
rs58871031 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698327 | AAAAAAATATATATA[-/T]ATATATATATATATA | 5521 |
rs58871902 | snp | A/G | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911110 | TTTTTTTGAGATGGA[A/G]TCTTGTTTTGTCCCC | 5521 |
rs58873710 | in-del | -/GTTTCCACATTTTTATAAG | 0.0337948 | 0.12552 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590961 | CCACATTTTTATAAG[-/GTTTCCACATTTTTATAAG]TTATCCCCTCTTAGG | 5521 |
rs58881270 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734106 | GTTGCTGAGGCTGGA[C/G]GGCAGTGGCATGATC | 5521 |
rs58881378 | snp | C/T | 0.0839998 | 0.186933 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912302 | CCTAAAGAGAGTGAC[C/T]TTATCATCTGAGGAA | 5521 |
rs58892818 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659325 | TACCTACTTTAAAAA[-/G]CTCAGGAAAGTACAT | 5521 |
rs58924217 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959040 | CATAGTAGCCTTAAT[C/T]TAACCAAAGCCAATA | 5521 |
rs58940771 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704741 | TTATTATTTTTTTTT[-/T]AAATCAATCTCAGCA | 5521 |
rs58947506 | in-del | -/TT | 0.49168 | 0.063958 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912513 | AACTTTTCTTTTTTC[-/TT]TTTTTTTTTTTGTTT | 5521 |
rs58952719 | snp | A/G | 0.0770498 | 0.180522 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083193 | TGAGATTTCTCCCCA[A/G]TTTTTGTCCTGGCAC | 5521 |
rs58956274 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632072 | TGTGCCCCCCCCCCC[-/C]GCCCATTCATATATT | 5521 |
rs59004522 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740535 | CCTCTTTCTTTTCCA[C/T]AAATTTGGATCTGCC | 5521 |
rs59015699 | in-del | -/AC | 0.405429 | 0.195811 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004270 | GGCAATCACTAGAAG[-/AC]ACACTGCCCCAGAGG | 5521 |
rs59020060 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862654 | ATGCTTTGAAGATCA[A/G]TTAGGAGAGACTTAA | 5521 |
rs59046328 | snp | A/C | 0.179425 | 0.239831 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619941 | TATTATCTGTTCAGG[A/C]TTCACAATGAGTTAA | 5521 |
rs59047673 | in-del | -/GCGCGCACACAC | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018039 | CACACACATGCATGC[-/GCGCGCACACAC]ACACACACACACACA | 5521 |
rs59075430 | in-del | -/CA | 0.334642 | 0.235236 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842376 | ATATTCTAAATCTAC[-/CA]CAGTCAACTTGCTAT | 5521 |
rs59092209 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886375 | AAATAAATAATAAAA[-/G]CTAAAATAAAATAAA | 5521 |
rs59230587 | snp | C/T | 0.401037 | 0.199218 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692586 | TCACCCAGGCTGGAG[C/T]GCAGTGGCACAATCT | 5521 |
rs59243961 | snp | A/G | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911637 | AAGACACTTCTTCAC[A/G]TGGGAGACTATTGCC | 5521 |
rs59289016 | in-del | -/GATCAGTAACTATTAGGTTGGTGCAAAAGTAATTGTGGATTTGCCATTTTTAATGGCAAAAACCACAATTACTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000620 | TGTGAACTCTATTAT[lengthTooLong]TGCACCAACCTAATA | 5521 |
rs59306681 | snp | C/T | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918408 | GAATGATGAAGTTGA[C/T]GATAATGGCAGCTTG | 5521 |
rs59329730 | in-del | -/ATAA/ATAAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886370 | TAAATAAATAAATAA[-/ATAA/ATAAA]TAAAACTAAAATAAA | 5521 |
rs59344782 | snp | C/T | 0.12932 | 0.218944 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688686 | GAGGATCTCTGCTCT[C/T]GTGGAAACTGAATAG | 5521 |
rs59362529 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738768 | GGAGGATATAGGTAG[A/G]GTTCTTTATTCTAGC | 5521 |
rs59371017 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005301 | ATGCCATAGTTAGTG[A/G]TGTAAACATACTTGA | 5521 |
rs59379734 | snp | A/C | 0.0349115 | 0.127424 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917565 | TATGCCCAAGGGCAC[A/C]CAATTAATGGTAGAG | 5521 |
rs59437403 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760578 | CAATTTAAAGCAAAT[A/G]TGCTCTAGATTTAAA | 5521 |
rs59451702 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698321 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 5521 |
rs59483273 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765323 | CACCTTGTACTAGGG[-/G]TAATTTTCAGAGTCA | 5521 |
rs59517598 | in-del | -/AA | 0.0452528 | 0.143452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673545 | GATAGTGGATCCTTT[-/AA]CCTGAGGGGAAATGC | 5521 |
rs59524033 | snp | C/T | 0.170084 | 0.236883 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616365 | GCAAGCACAAGCAAC[C/T]AAAGCAAAAATGAAC | 5521 |
rs59572002 | snp | A/G | 0.409552 | 0.192466 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719913 | ATATGGCCATTCCTG[A/G]CTTGAGTGGGGAAGC | 5521 |
rs59640348 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999478 | TCCCCAGAGATTCTG[A/C]TTTACTTAGTTGGGA | 5521 |
rs59645635 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686695 | TGTAACAGGTAAAAA[C/T]GCCGATTTCAACCTG | 5521 |
rs59693705 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758017 | GAAACCTCTCAGCTA[C/T]TCAGACCTGTCCAGA | 5521 |
rs59713747 | in-del | -/GTTTTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845321 | TTTTTTTGTTTTTTT[-/GTTTTTT]TTGAGATGGAGTCTC | 5521 |
rs59774081 | snp | C/G/T | 0.0391387 | 0.134304 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991308 | TCATAATAGCCAAGA[C/G/T]AGGAAATCAACCTAT | 5521 |
rs59815477 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848858 | ATTTTCTCCTCCTCT[A/C]CTATTTATTCAATTA | 5521 |
rs59819552 | in-del | -/TAATAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886374 | TAAATAAATAATAAA[-/TAATAA]ACTAAAATAAAATAA | 5521 |
rs59828501 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024639 | TCTGGCCACAAAAGA[A/T]TAAATTAGAAATTAA | 5521 |
rs59852193 | snp | G/T | 0.137527 | 0.223271 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738255 | CAAAAAATTAGCCGG[G/T]CGTGATGGCGGGTGC | 5521 |
rs60023359 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980504 | AACAGAGCTGGAAGA[A/G]ACAGCAACAAGGAAA | 5521 |
rs60041254 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726257 | AAGCAGGAAGAAAAC[A/T]AGGATTTTGGCCAAT | 5521 |
rs60056635 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863060 | TCCACAGTGCACAGA[A/G]ATTTGTAGGTCCTGG | 5521 |
rs60057388 | snp | C/T | 0.0581099 | 0.160244 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687052 | GTGTGGCAGGGACAG[C/T]GGTAGCGGGGAGTGG | 5521 |
rs60087042 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704503 | ACTACAAACTTGAGC[A/G]TTTTTCCTCTGTTGT | 5521 |
rs60151742 | in-del | -/A | 0.257454 | 0.249889 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842487 | TCCATGCCCTTTTTT[-/A]TTTTTTTTTTTTAAA | 5521 |
rs60161356 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018079 | CACACACACACACAC[-/AC]TTAGAAGCGTTAAGC | 5521 |
rs60166631 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908540 | TTTTTTTTTTTTTTT[-/T]GGCATAGGGGTGTGT | 5521 |
rs60219345 | in-del | -/T | 0.397271 | 0.202018 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031478 | ATTGCTTTTTTTTTT[-/T]AATTTATCTTGACTG | 5521 |
rs60219413 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029903 | ACCCAGTCTCTGATA[A/T]TCTGTTATGGCAGCC | 5521 |
rs60241637 | snp | C/T | 0.104504 | 0.2033 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080118 | TTAAATAAACTGCCT[C/T]TTTCAAATTCCTCAG | 5521 |
rs60279771 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903994 | TTCTAAACATGCTCC[A/G]GGGTTTCCTGGCTCA | 5521 |
rs60327278 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600151 | ATCCTGTGGCACTTA[C/T]AGCCTGTACCATTTT | 5521 |
rs60345774 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869086 | TTAATTATTAACATT[C/T]AAATCCACAATGGTT | 5521 |
rs60367248 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738814 | ATAAAACTAATTATA[C/T]TGAGGGTTTTTTAAT | 5521 |
rs60395374 | in-del | -/CACACACACACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740610 | ACACACACACACACA[-/CACACACACACACA]GATAAAAGTTCTTGA | 5521 |
rs60404078 | in-del | -/CA/CACACACACA/CACACACACACA/CACACACACACC/CACACACC | 0.625 | 0.125 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053572 | ACACACACACACACA[lengthTooLong]ACCTCAGATGTATAC | 5521 |
rs60459414 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030023 | AGAATTAGCTTTTCA[C/G]TTTCCACAAAAACAA | 5521 |
rs60522229 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051780 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAT | 5521 |
rs60522338 | in-del | -/ACAT/AT/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800945 | CACACACACACACAC[-/ACAT/AT/CA]ATATACACACATGTA | 5521 |
rs60548705 | snp | C/G | 0.136847 | 0.222927 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633784 | TGGGGCTCCCTGGGT[C/G]TGTGGCTTGACCGGC | 5521 |
rs60563072 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062709 | CACCAAGACTGACAC[G/T]AAGATTTTGTATCTG | 5521 |
rs60586896 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698329 | AAAAATATATATATA[-/T]ATATATATATATATA | 5521 |
rs60613272 | in-del | -/CACACACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740614 | ACACACACACACACA[-/CACACACACA]GATAAAAGTTCTTGA | 5521 |
rs60621327 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681191 | AATGCATAATGAGCA[A/G]AGGCCCTAGAAGTCC | 5521 |
rs60690294 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840509 | AGTCAAACTGTGATT[A/T]AAAAGCACAGCCCTA | 5521 |
rs60713115 | snp | A/G | 0.316726 | 0.240931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736183 | CTCCATGTGAAGAAG[A/G]ATGTGTTTGCTTCCC | 5521 |
rs60753702 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999038 | AAAAAAAAAAAAAAA[-/A]GAGTCAATCTCTGGT | 5521 |
rs60754040 | in-del | -/GAAAGAGA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745206 | AGAGAGAGAGAGAGA[-/GAAAGAGA]CTATAAGCATGGAAT | 5521 |
rs60803545 | snp | C/T | 0.222928 | 0.24853 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062305 | AATTGCCTAATATTA[C/T]TCTTCTCAGAATGTT | 5521 |
rs60817911 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071328 | CAATAACCTTTCAAC[C/T]GATTCCTGCTTCTGA | 5521 |
rs60848399 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698325 | AAAAAAAAATATATA[-/T]ATATATATATATATA | 5521 |
rs60850929 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643783 | GCATATGGTATAATC[A/C]CAACTATATACAAAA | 5521 |
rs60877450 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880224 | GTGTGTGTGTGTGTG[-/TG]GTGGGGGGAGTTCAG | 5521 |
rs60946617 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775097 | ACTCTTTCAAAAAAA[-/A]CGAAAACAAAAACAC | 5521 |
rs60956270 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834700 | TTACATGAGTAAATT[C/G]TGTGTGTTGAGACTT | 5521 |
rs61005237 | snp | C/G | 0.247621 | 0.249989 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607540 | GATGAAGAATGAAAA[C/G]TTAATCTAGAAGAAA | 5521 |
rs61024428 | snp | G/T | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021636 | AGCCACAGGGTGATA[G/T]CTAATCTAGATTCAT | 5521 |
rs61056451 | snp | A/G | 0.162253 | 0.234095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633551 | GTTGGTTCTTTGAAG[A/G]AGTCAGGAAAATGAA | 5521 |
rs61061981 | in-del | -/TATATA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772427 | ATATATATATATATA[-/TATATA]CTTATTTCTAAATAC | 5521 |
rs61088380 | snp | A/G | 0.325799 | 0.238232 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980614 | CCTGTGGAACTAGAT[A/G]GGCTGGGAAAGACTT | 5521 |
rs61176886 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827708 | GTATTGATAAAGTAT[C/T]GACTCCATGCACAGC | 5521 |
rs61225211 | snp | A/C/G | 0.0570088 | 0.160747 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001835 | TTCTAACAACCCCCA[A/C/G]CTCTTCGGAGTTGGG | 5521 |
rs61283179 | snp | A/T | 0.285257 | 0.247501 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828262 | ACTTTTACTTTTTTT[A/T]AAAAAAAAAAAGACA | 5521 |
rs61300524 | in-del | -/GTT | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976125 | ATTATTATTATTATT[-/GTT]ATTATTATTATTATT | 5521 |
rs61314158 | snp | C/T | 0.427423 | 0.176128 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701590 | AGGATGCTTGAAGCT[C/T]AGACATGGAAAATGG | 5521 |
rs61326177 | snp | C/T | 0.0509478 | 0.151255 | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878692 | TGCAGCCGGCGCCAG[C/T]GCACTCACCCTCACA | 5521 |
rs61333046 | snp | C/T | 0.411242 | 0.191052 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009898 | ACACACACACACACA[C/T]ATATATATATAGGAC | 5521 |
rs61413711 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780472 | TACTGATTCAGACTT[A/T]AAAGGCTGACTGTCC | 5521 |
rs61418418 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601265 | TAAGTTTTTGTCTGG[C/T]CATATGTTTTCATTT | 5521 |
rs61438640 | snp | A/G | 0.498547 | 0.0269177 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693752 | GTCACAGCATGGAGA[A/G]TGTTTAACACAGTAT | 5521 |
rs61445378 | in-del | -/TTTTTTTTT | 0.0588605 | 0.161139 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641504 | TTATGTGCTCTAAGA[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 5521 |
rs61468966 | in-del | -/TCA | 0.349897 | 0.247154 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686619 | TTCGAAAAATTGTAT[-/TCA]TCATCACATCACCTT | 5521 |
rs61574273 | in-del | -/TACACACAGA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733709 | AAAACCACACACAGA[-/TACACACAGA]CACACACACACACAA | 5521 |
rs61589463 | snp | A/G | 0.116488 | 0.211364 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788890 | CTCTCAGTTTCTTCC[A/G]GAGACCTTAGCATCA | 5521 |
rs61627537 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836212 | GTTGGTATGTCACTG[A/G]TTACGTTTTCCAATG | 5521 |
rs61636626 | snp | C/T | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911240 | AGGTGCACACCACCA[C/T]GTCCGGCTAATTTTT | 5521 |
rs61642938 | in-del | -/T | 0.131038 | 0.219882 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635344 | AACATGTGTCATGGG[-/T]TTTTTTTTTGTGTGT | 5521 |
rs61749639 | snp | A/G/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691134 | TGCACTCACCCGCAG[A/G/T]GTTGTGATGGTGGCA | 5521 |
rs61784966 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977778 | caatccaaatgccca[C/T]caacagtagactgga | 5521 |
rs62373271 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807308 | TCATGGCTAAGGAGG[A/C]ATGGCAGTATGTTTT | 5521 |
rs62373273 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814210 | AAAAAAAAAAAACCC[A/T]CCATATCCTATGGTC | 5521 |
rs62373274 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825161 | TTCCCCTGGGTTTCA[C/T]AGAGCCGACGTTATC | 5521 |
rs62373275 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825348 | ACTTCCATGTTTATT[A/T]GGAAAAAGAAAACAC | 5521 |
rs62373277 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845436 | TTTTTTGCACTTTTA[G/T]TAGAGACGGGGTTTC | 5521 |
rs62373278 | snp | A/G | 0.229723 | 0.249176 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846104 | ATTTTATCTGGCCAG[A/G]TGCAGTGGCTCACGC | 5521 |
rs62373279 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847354 | AGGCTCCTCACACCA[G/T]TCATTCTGAACTCCA | 5521 |
rs62373280 | snp | C/T | 0.23031 | 0.249223 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848554 | TTGATGTTTTTCTCG[C/T]GATTGAAGACCACAG | 5521 |
rs62373281 | snp | G/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861873 | TTTTTTTTTTTTTTG[G/T]CTTGCTGCTTTCATC | 5521 |
rs62373289 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862761 | GGGTCAAAGAAAAGT[A/T]AATTTTTTTTTTTTT | 5521 |
rs62373290 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866693 | TATACATCATATGTA[A/G]TATACCATAGATACA | 5521 |
rs62373291 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871827 | ATGTTTGTAATACAT[A/G]TGTATTTGTTATGCA | 5521 |
rs62373292 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894692 | TGATCCACCTGCCTC[A/G]ATCTCCCAAAATTCT | 5521 |
rs62373293 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896701 | TCCTTTTTTTTTTCG[G/T]TGATTCACTTTCCTG | 5521 |
rs62373294 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899063 | TTGTGGAAGTCAGTA[G/T]GGCGATTCCTCAGGG | 5521 |
rs62373311 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908994 | CTGGGTTTACTTTAA[A/G]ATCCTTCAGATCAGC | 5521 |
rs62373312 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915481 | ACACACACGTACACA[C/T]GTGTGCAATTTACAT | 5521 |
rs62373313 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915922 | TTAAGAAAACTTACT[A/G]CCTCATTACTCTGAA | 5521 |
rs62373314 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922732 | AGTTCTAGAGTAGAA[C/T]TCTGGGTGGTTTAAG | 5521 |
rs62373315 | snp | A/G | 0.403684 | 0.197183 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930215 | TTATACTGAGAGCTG[A/G]TCAGTGAGGATCCAG | 5521 |
rs62373316 | snp | C/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932797 | TGTGATCATGATAAA[C/G]AAGGTCAAAGAGCAG | 5521 |
rs62373339 | snp | A/G | 0.354235 | 0.227234 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951599 | CTCACTTATAAGTGA[A/G]AACCTGAGGTGTTTG | 5521 |
rs62373340 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951993 | TTTTTTTTTTTTTTT[A/T]AAAGCTCCTCAGTGA | 5521 |
rs62373341 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951997 | TTTTTTTTTTTTAAA[G/T]CTCCTCAGTGACTTA | 5521 |
rs62373342 | snp | A/G | 0.323197 | 0.239044 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962476 | AGCCTGACCAACATG[A/G]TGAAACCCCGTCTCT | 5521 |
rs62375668 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678797 | TCCCATTCACAATTG[C/T]TTCAAAGAGAATAAA | 5521 |
rs62375671 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687130 | AGGGAGCGATTGATC[A/G]ATTAATCCCCTCACC | 5521 |
rs62375672 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703372 | GGGAGCCAGGCCTGA[G/T]GTTTACAATGCCTGG | 5521 |
rs62375673 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713425 | TGCCACCAAACTGTA[C/T]ACTGAAAAATAGTTA | 5521 |
rs62375674 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718697 | CACCCTTTCAATTTG[C/T]AGGAAGAAAGGCAAT | 5521 |
rs62375675 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731641 | GGAGAGTCAGTCACC[C/T]TCATTCTCAATTTCC | 5521 |
rs62375676 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743576 | CCTTCTCCATCCCCA[C/T]GTCTAATCCAGTTCA | 5521 |
rs62375678 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747870 | GTGAATTTTTTTTTG[G/T]CCCAAGAACAGCATG | 5521 |
rs62375679 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751050 | AGGGATGGCTCCCCA[A/G]AGAAGTGGATTTACA | 5521 |
rs62375680 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761785 | GTATGAGGAGATGTT[C/T]GTAAAACACCTAGCA | 5521 |
rs62375682 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796695 | TACAAACCTAGGGTA[C/G]AAAAGGAAACTAATC | 5521 |
rs62377576 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967232 | GAGTTTTGGTTAAGC[A/C]TTTGTAAGAAGCCTT | 5521 |
rs62377577 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972690 | GTACTCCAGCCTAGG[A/C]AAGAGAGTAAGACTC | 5521 |
rs62377578 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978217 | TGCCCACTTTTTGAT[G/T]GGTTTTTTTTAATTG | 5521 |
rs62377580 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994059 | CTTAAGGTCAAGGCA[C/G]ACAGTCAAAAAACCT | 5521 |
rs62377581 | snp | C/T | 0.307176 | 0.243374 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997406 | ACAAGGCAGTAAGCC[C/T]TCCAGGTAGACATTC | 5521 |
rs62377583 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014351 | CAGGGATCTAGAACT[A/G]GAAATACCATTTGAC | 5521 |
rs62377584 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018039 | CACACACATGCATGC[A/G]CGCGCACACACACAC | 5521 |
rs62377604 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021272 | CCCTGGGGTAAGAAA[C/G]GGGCACCCAAGGAAA | 5521 |
rs62377605 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030727 | ATCTTACTACTTCCC[C/T]GAAAGTCTAAGAGAG | 5521 |
rs62377606 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046076 | TAGATTAATTTATTT[A/G]CCTTCCATAAGAGCA | 5521 |
rs62377607 | snp | C/G | 0.361474 | 0.223771 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052184 | GTTCCTTAAAGTATG[C/G]TTACAGAAAGCTCCC | 5521 |
rs62377608 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147056058 | TGCCTGTAAACACAC[A/G]CTGAAATGCTCTGCC | 5521 |
rs62377609 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062912 | TCCTAGGACATGGTG[C/T]CAAGGACTGTGAGAT | 5521 |
rs62377610 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063011 | GAGGGGGGAAGAAGG[A/G]AAGGGGGAAGAGAGG | 5521 |
rs62377611 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063023 | AGGGAAGGGGGAAGA[A/G]AGGAAGGAGAAAAGG | 5521 |
rs62377631 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074977 | TATGTTGACAGACAT[C/G]AAAGAACTGCAGAGT | 5521 |
rs62377632 | snp | C/T | 0.122064 | 0.214785 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075832 | CACATTGTCTCTCAT[C/T]AGACTTCCTATAAAG | 5521 |
rs62377633 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077515 | TTATTGACTTTGAGC[A/G]TATAGAAAATTAGGG | 5521 |
rs62377634 | snp | A/G | 0.116488 | 0.211364 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079246 | TAAATAATAAAATCA[A/G]TACATAGAAGAGAAA | 5521 |
rs66470287 | snp | C/T | 0.334412 | 0.235318 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817921 | ATCCTCCCATTTGCT[C/T]ACACTGCTCTGCACC | 5521 |
rs66510326 | in-del | -/TGT | 0.478271 | 0.101943 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973076 | GATGATCTTTAAAAA[-/TGT]TCTGTGGTATCCTTT | 5521 |
rs66565440 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845314 | CATCTCAAAAAAAAA[-/C]AAAAAAAAGAAAAGG | 5521 |
rs66605427 | snp | A/G | 0.2776 | 0.248472 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609296 | AAGATTTGGAACACG[A/G]CAAAGATGCCCACTG | 5521 |
rs66668306 | snp | C/T | 0.447032 | 0.153878 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685759 | ACTGTGAGTGTCCTG[C/T]GCTGACAGGAGGACA | 5521 |
rs66710944 | in-del | -/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936529 | CATGTCTTGTTTTTT[-/C]TTTTTTTTTTTTTTG | 5521 |
rs66769556 | snp | C/T | 0.2462 | 0.249971 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685015 | GTCTCCTCCATGCCC[C/T]CTAAGGACAGAGAGT | 5521 |
rs66933047 | in-del | -/ATTA | 0.416218 | 0.186739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668188 | GTCCTAAAGAAAACG[-/ATTA]ATTCTCTAGCTTCCT | 5521 |
rs66941614 | in-del | -/ACACACAGAT | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733700 | AAGGAAAACAAAACC[-/ACACACAGAT]ACACACAGACACACA | 5521 |
rs67055347 | snp | A/C | 0.277867 | 0.248442 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609026 | TACAAAAATCCTCAA[A/C]AAAATACTAGCAAAC | 5521 |
rs67167992 | snp | C/G | 0.362313 | 0.223351 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682111 | TCTGCTTATATTTAC[C/G]TCTATGTTGGATCTA | 5521 |
rs67308237 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838571 | CAAAAAAAAAAAAAA[-/A]GAAAAAAAAGAAGGA | 5521 |
rs67341491 | in-del | -/TATATATATATATATATATATATATATA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772405 | GTATTTAGAAATAAG[-/TATATATATATATATATATATATATATA]TATATATATATATAT | 5521 |
rs67467435 | in-del | -/ATATATATATATATATATATATATATAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772384 | GTTAATAACTTGTGC[-/ATATATATATATATATATATATATATAT]ATATATATATATATA | 5521 |
rs67481128 | in-del | -/CGCGCGCACACA | 0.159951 | 0.233219 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018038 | ACACACACATGCATG[-/CGCGCGCACACA]CACACACACACACAC | 5521 |
rs67551935 | in-del | -/AGG/GAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782817 | AAGGGAGAGGAAASA[-/AGG/GAG]GRAGAAAGAAGGAAA | 5521 |
rs67810307 | in-del | -/GAGAGAGAGA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764801 | GAACATCTCTATCCC[-/GAGAGAGAGA]GAGAGAGAGAGAGAG | 5521 |
rs67818938 | snp | A/C | 0.375996 | 0.215928 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682680 | TAATACATACTTAAT[A/C]AATGTCTGCAATAGT | 5521 |
rs70998100 | in-del | -/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665014 | CAGCAAAGCCTGAAT[-/G]AGAGCACATCTGTTT | 5521 |
rs70998101 | in-del | -/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702075 | TAATTCCCCTGCCTC[-/T]TTTTTTTTTTTTTTT | 5521 |
rs71001403 | in-del | -/TCTCTT | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745208 | ATTCCATGCTTATAG[-/TCTCTT]TCTCTCTCTCTCTCT | 5521 |
rs71001404 | in-del | -/CTC | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782818 | TTTTCCTTCTTTCTT[-/CTC]CTGTTTCCTCTCCCT | 5521 |
rs71001405 | in-del | -/AAAAAAAAAAAAAAAA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807800 | CAAAACTGTCTTCTC[-/AAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 5521 |
rs71001406 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845322 | TGAGACTCCATCTCA[-/A]AAAAAAACAAAAAAA | 5521 |
rs71001408 | in-del | -/AGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAA | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900587 | GAAGGAAAGAAGGAA[lengthTooLong]GGAAGGAAGGAAGGA | 5521 |
rs71274371 | in-del | -/CCT | 0.245916 | 0.249967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782816 | TTCCTTCTTTCTTCT[-/CCT]GTTTCCTCTCCCTTC | 5521 |
rs71581877 | in-del | -/G | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615370 | GTCGGGGGAGGGGGG[-/G]AGGGATAGCATTGGG | 5521 |
rs71581879 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815070 | CAGTAGAAGGAGACA[CA/TG]GAAGCCATCTATCCT | 5521 |
rs71581881 | in-del | -/TTTT | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861868 | ATTGTTTTTTTTTTT[-/TTTT]GGCTTGCTGCTTTCA | 5521 |
rs71581882 | in-del | -/ACAC | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865294 | CTCTCTTTGTCTCTG[-/ACAC]ACACACACACACACA | 5521 |
rs71581883 | in-del | -/A/G/TA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886825 | CATTTTAAACTTTTT[-/A/G/TA]GTAAAAAAAAAAAAT | 5521 |
rs71586438 | multinucleotide-polymorphism | AG/GA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941510 | CTGAACACACCCCTA[AG/GA]CAACAGAAGCATCAT | 5521 |
rs71586439 | in-del | AAGGAC/GGAT | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907484 | ACTTTGCCCTTCTGT[AAGGAC/GGAT]ATTAATTCCACTTTC | 5521 |
rs71586440 | in-del | CTTCTC/TTTCTCA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811579 | AACAGAGTGAGATTC[CTTCTC/TTTCTCA]AAAAAAAAAAAAAAA | 5521 |
rs71592192 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667336 | AATAGGCGTGTGCAC[A/G]CACACACACACACAC | 5521 |
rs71592193 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679238 | CCTCAGAAATAACGC[C/T]GCATATCTACAACTA | 5521 |
rs71594539 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687088 | GGAGGGAGAGAGAGG[G/T]AGAGGAAGAGAGGGA | 5521 |
rs71594540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706301 | CTGGTGCGGCTGAAG[A/G]AGCTGGAACCTGCGC | 5521 |
rs71594541 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712366 | TGCAATACTGTACAC[A/C]CAGTAGGTAAGAGTA | 5521 |
rs71594543 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812768 | TCACTAGAGTTACTT[A/T]ATGTGTGTGTGTGTG | 5521 |
rs71594544 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832453 | CTGGAGTGCAGTGAA[A/G]CGATGTTGGCTCACC | 5521 |
rs71594545 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832527 | CTCCCAAGTAGCTGA[A/G]ATTACAGGTGCCTGC | 5521 |
rs71594546 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939397 | CGTTCAAGGTCCTGC[A/G]AGTGGGAAAGAGGGT | 5521 |
rs71594547 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989798 | AATTTTAAAAAGTGG[A/G]AGTCATATTGTCCCT | 5521 |
rs71821729 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018044 | ACATGCATGCGCGCG[-/CA]CACACACACACACAC | 5521 |
rs71877850 | in-del | -/A | | | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767072 | AAAAAAAAAAAAAAA[-/A]GGCTCAGCAGAGACA | 5521 |
rs71965794 | in-del | -/TGTC | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911089 | TGTTAGACACTTTCT[-/TGTC]TTTTTTTTTTTTGAG | 5521 |
rs72300042 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822535 | TTTTCTTCATTTTTG[-/GT]TTTTTTTTTTTTTTT | 5521 |
rs72462832 | in-del | -/AT | 0.495407 | 0.0477027 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075944 | GTTATGTTGTTTAAA[-/AT]ATATTTCTAATTATA | 5521 |
rs72464644 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698352 | TATATATATATATAT[-/AC]ACACACATATAATTA | 5521 |
rs72543437 | in-del | -/AC | 0.499942 | 0.00539106 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972209 | GATTAGAATGGGGTT[-/AC]AGTTTTTGGAAGGAA | 5521 |
rs72652834 | snp | C/T | 0.262159 | 0.249704 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606567 | AATCACTTAGCAAAG[C/T]GTCTGTACCCAAAAC | 5521 |
rs72652835 | snp | A/G | 0.223522 | 0.248594 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618087 | AGAACCTGTGACCAC[A/G]TTATGTTACATGACA | 5521 |
rs72652836 | snp | C/T | 0.176219 | 0.238865 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625697 | GCAGAATGATGGCTC[C/T]CCAAGGATGTCAAAA | 5521 |
rs72652837 | snp | A/C | 0.136847 | 0.222927 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633027 | CCACCGATACTCATG[A/C]GTGGAAAGGGGAAAG | 5521 |
rs72652838 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643359 | ATCCATGGAGCCTAT[A/T]TTCTAGTAGGGAACA | 5521 |
rs72652839 | snp | A/C | 0.16976 | 0.236773 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654330 | GCTGGGGGCTAGGAT[A/C]TGAAGCCAGTTAATT | 5521 |
rs72652840 | snp | A/G | 0.357238 | 0.225832 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665285 | TTTAGTGTAGCCACC[A/G]CCACCCATGATCTTA | 5521 |
rs72652841 | snp | C/T | 0.357664 | 0.225629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670774 | TACTGGGATTATAGG[C/T]ATGAGCCACTGCACC | 5521 |
rs72652842 | snp | C/T | 0.17332 | 0.23795 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682150 | ATGGTAAGTGCAGCA[C/T]AACAAAGGTACCTTT | 5521 |
rs72652843 | snp | C/G | 0.175254 | 0.238565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685864 | CCTGTGGCAGAAAAG[C/G]CTCTGCAGCCCTCAC | 5521 |
rs72652844 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694804 | CAAATTTTGTGATTT[C/T]TTTTATATTTATGTA | 5521 |
rs72652845 | snp | A/G | 0.286564 | 0.247312 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695070 | AGGAAATACTATGTG[A/G]TCATTATGATATTTT | 5521 |
rs72652846 | snp | A/C | 0.304937 | 0.243889 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705504 | AGCACAGAGGCTTCT[A/C]GCTAGACTGGCAATG | 5521 |
rs72652847 | snp | A/G | 0.236144 | 0.249616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709661 | ATGTGTTCATAATAC[A/G]TGGGGCTGTGGCAGC | 5521 |
rs72811852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642582 | ATAGTGCACAAAATT[A/C]TAACAACAGTTTGAT | 5521 |
rs72811875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681822 | GGTTAGGGAAAGACA[A/G]TGTGTCAGAGCCTGT | 5521 |
rs72813707 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752083 | CAGAGAACAGATGGT[A/G]GATAGAAATCTGTTA | 5521 |
rs72813708 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757686 | TGTACAAACATGCGA[C/T]ATGGGGGAAGGAAAG | 5521 |
rs72813709 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760335 | CTGCATAGCTAGTAA[A/G]TAGAAAATTAAGCTT | 5521 |
rs72813710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765222 | CATACATTATAAGAT[A/G]TAGTTTTCATATGAT | 5521 |
rs72813712 | snp | A/T | 0.279461 | 0.248258 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769387 | CTTCAGGTGATTCTG[A/T]TACAGGCTAAAGTTT | 5521 |
rs72813713 | snp | C/T | 0.247905 | 0.249991 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769460 | ATCGTAAACTATAAT[C/T]GTTTCTTCTTATTAT | 5521 |
rs72813715 | snp | C/T | 0.29175 | 0.246489 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777155 | TTGAAAACAGTGACT[C/T]AAATAGATACTTATA | 5521 |
rs72813717 | snp | A/G | 0.293551 | 0.246177 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781190 | TAAAATTATTCTCAT[A/G]ATATAAGTGAAGAAA | 5521 |
rs72823280 | snp | A/G/T | 0.0311738 | 0.121636 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809617 | AGCAGCTAGCCTGCA[A/G/T]CCAGAGCTTAGTAAG | 5521 |
rs72823282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810603 | CAGCCAGGATTTGAA[C/T]GCTTGTCTATGAGCA | 5521 |
rs72823289 | snp | C/T | 0.311123 | 0.242413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831888 | GCTCCATGCATCTTA[C/T]TGCCTTTGAAGGCCT | 5521 |
rs72823296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845090 | GATTCTTTGCATATG[C/T]GACAAGCCTCAGGGC | 5521 |
rs72825203 | snp | C/T | 0.366885 | 0.220993 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857185 | ACAACTTCTATGCAA[C/T]AGGAACTATTCAGGA | 5521 |
rs72825208 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877576 | GGGCAGGAAATGAAA[A/C]CTTGCCCTCCCTGCA | 5521 |
rs72825210 | snp | A/G | 0.298651 | 0.24522 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881773 | ATTATATTTGTTGGA[A/G]ACAAACATTTCTTAA | 5521 |
rs72825229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900702 | GGTAAATGTGTGTCA[C/T]GGTGATTTGCTGTGC | 5521 |
rs72825252 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915308 | CTGCCACTTGGATTC[A/G]GAGAAAAATTCAAAT | 5521 |
rs72825256 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931580 | TTTTGAGGCATTTCA[C/T]TATTCCTAGCAACTC | 5521 |
rs72825261 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944431 | CAAGGAAACGCCAAA[C/T]GATTTGAAAGGTTCA | 5521 |
rs72825263 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948918 | GCTGTACATAAGACT[C/T]ATCTAAGGACTTTGC | 5521 |
rs72825264 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952574 | GCTGCCCAGTTCCAA[C/T]CCTTTCTCAGCTAGA | 5521 |
rs72825267 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965764 | TGCACTTATCTTGAT[A/C/G]ATAATTCTTCTTAAA | 5521 |
rs72825286 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997588 | CAGTTGATCTTGATG[A/C]ATGCCAACATGTGAG | 5521 |
rs72825287 | snp | C/T | 0.0257331 | 0.110473 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000078 | TGATGATGGTGACTT[C/T]AACAGACAGAGGGAT | 5521 |
rs72825288 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009745 | CATACAGATATTTGG[C/G]ATACATAGACATGGC | 5521 |
rs72827248 | snp | A/C | 0.241914 | 0.249869 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024262 | AAAGGGTCAGTACAT[A/C]AGAAAGACATTAATA | 5521 |
rs72827249 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025097 | AGAAATGACAGAAGG[G/T]ATCTCATTATAGGTC | 5521 |
rs72827251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033264 | AATAACCACCCATGT[A/G]CATGGCTTTAACTAC | 5521 |
rs72827252 | snp | G/T | 0.289424 | 0.246872 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035624 | TATTCTGTTATCCAA[G/T]AAACAAAATTACATG | 5521 |
rs72827256 | snp | G/T | 0.304438 | 0.244001 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040257 | ATTCAAATAAATAAT[G/T]TTGTATGATACCCTA | 5521 |
rs72827259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053437 | ACTTTCACAGAGATA[G/T]TCACACACTATTCAT | 5521 |
rs72827261 | snp | C/T | 0.300421 | 0.244863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054174 | TGATATAGAATGTTT[C/T]GTTTAATTAATACAC | 5521 |
rs72827264 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056440 | GATAGATTCTGTGCT[C/T]CACTACTGCCTCTTT | 5521 |
rs72827265 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057295 | AGACCCAGGGACTTG[G/T]CAAGGTAGGGCCATC | 5521 |
rs72827272 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066715 | TCTTAATGCCTTTCT[C/T]GGACTGCTAGAAAGC | 5521 |
rs73307037 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834417 | CTCCTTTACACTGCC[C/T]TTCTTGGCAAGTTGA | 5521 |
rs73307071 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855375 | GAGTCTCTATAAATG[C/T]ATAATGCTAACATTG | 5521 |
rs73307078 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923636 | GGAGTGCAAATTAAT[G/T]CAGCCATTATTGAAG | 5521 |
rs73307081 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927512 | TCTCTAAACACCGCT[A/T]GCCATCTATCCTTAG | 5521 |
rs73307084 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942390 | AAATGTTCTTTTCTT[A/T]TACCGTCAGAAATAA | 5521 |
rs73310544 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632255 | AGGCAGTGTAAAGAC[A/C]CAGGGAGAAGACAGC | 5521 |
rs73310555 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635241 | AGAGCTGAGTTCTGA[C/T]TCCAAAGCATCTGCT | 5521 |
rs73310563 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638159 | CTCCTAGTGTGTCTG[C/G]TGTAGAAAGGGAGAT | 5521 |
rs73310568 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641264 | GCAGAGCTGGGATTT[A/G]AACCCAAGCTTGTCT | 5521 |
rs73310578 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646180 | ATTTTCATGCCTGGC[A/G]CAAACTAGGTGCTCA | 5521 |
rs73310616 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063331 | ACAGTAACAGTTTTA[C/T]TAAAACAGCTAAAAT | 5521 |
rs73310622 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063749 | TTAGAGCCTTCCCCA[A/G]GATTAGGCAGCATAT | 5521 |
rs73310627 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066288 | TAACATTAATAATGA[C/T]AGAGCAAGCATTTAT | 5521 |
rs73310630 | snp | C/T | 0.100588 | 0.200439 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068109 | AAAAAAATAATGATC[C/T]GGGTGGTAGAATGAT | 5521 |
rs73310631 | snp | G/T | 0.0792508 | 0.182605 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068410 | TTCTCTTAACTATGG[G/T]AAAGTCTTTCTAATG | 5521 |
rs73310633 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069281 | AGCGAAAACAAAACA[A/G]AAAGAGTTGAGTTTA | 5521 |
rs73310644 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070780 | CCTTGCTGCAAAGCC[A/G]AGATTTTGTTGTGGC | 5521 |
rs73310645 | snp | A/G | 0.046775 | 0.145601 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070935 | GTGGAGATTGCAGTG[A/G]TCCGAGATTATGCCA | 5521 |
rs73310647 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071564 | ACATACCAGATAAGC[C/T]CTTGCCTCAGGGCAA | 5521 |
rs73310648 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072815 | ACCTGAGCAAATAGC[A/G]CAAGAGAATAATTGA | 5521 |
rs73310655 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074992 | CAAAGAACTGCAGAG[C/T]GAGGAACAAACAAAG | 5521 |
rs73310665 | snp | A/T | 0.0944967 | 0.195752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076536 | TTTTCTACACTGAGA[A/T]TATATTGTTTAAGTA | 5521 |
rs73310669 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077339 | CCCTAGCCCTTATAG[C/T]CATAATGGGTAACTA | 5521 |
rs73310672 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077759 | TTTCTGCCTGTATTC[A/G]CTATTTTAAAGTGCA | 5521 |
rs73310677 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078839 | AAAATTGTATCACCC[C/T]GACCCTTGAAACTCT | 5521 |
rs73310845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980244 | TCCCAACTAGATGTT[A/G]GGCATATACTGAAGA | 5521 |
rs73310863 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986955 | AGACTATCTTAAGGC[A/G]TATAATAAACTCTCA | 5521 |
rs73310870 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988570 | TTTCTTGGGGCAAAT[C/G]AAAATGGAAACAAAA | 5521 |
rs73312656 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659411 | GGGTTTTTAGAGTTA[C/T]GTGGACTTGGGCTTG | 5521 |
rs73314891 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011018 | GCTGCCCACGTCACT[G/T]AGGGAAAAAGCCAAA | 5521 |
rs73316507 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020212 | TCAATTCCCTCTTGG[C/T]ATTTGATCCTGGAGA | 5521 |
rs73316575 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025535 | TTCTTAGATATGACA[C/T]CAAAGCATGATCTAT | 5521 |
rs73316577 | snp | A/G | 0.089084 | 0.191327 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027710 | AGTAATCTTTTTGGG[A/G]TGATTGAAATGTTCT | 5521 |
rs73316582 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028879 | CCATTCTGATCAGTA[A/T]GTCGTGGTATTCCAT | 5521 |
rs73317437 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592751 | TAACATTAAGGTGTT[A/G]TCTGTGCCAGTTCAG | 5521 |
rs73317439 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592783 | AACAGGATTCAAAGG[C/T]CTTACTACATCCTTC | 5521 |
rs73317445 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596001 | GTTCTTATATTTCAA[A/G]TGTTGACAAACTTTT | 5521 |
rs73317448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596327 | AAATGTATAATAGTA[A/G]CATTACCTGTCTCCT | 5521 |
rs73317453 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599906 | GTTCATGGCAGTTAA[G/T]ACTCAGTTTAAGGGT | 5521 |
rs73317456 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600126 | CTCTCCACATGTACC[G/T]TTATCTTAAATCCTG | 5521 |
rs73317457 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600910 | ATTTAGAATATGTTC[G/T]TTACCTCCCCCCAAA | 5521 |
rs73317459 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603257 | GAATTTGGGACCAAG[A/G]AGTACAGAACCTGCG | 5521 |
rs73317460 | snp | C/T | 0.121717 | 0.214577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603587 | GATAACATACCAGCA[C/T]AGCACTTTGTAGTTC | 5521 |
rs73317461 | snp | A/C | 0.121717 | 0.214577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603636 | TTCAAGTTTTAATAG[A/C]AGCTCCAGGAATTAT | 5521 |
rs73317463 | snp | A/G | 0.121717 | 0.214577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603703 | TAATTACTTTTGATG[A/G]GAAGCTTATAATACT | 5521 |
rs73317473 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616677 | CAAAACTACAATTAG[A/G]TATCATCTGACCCTA | 5521 |
rs73317479 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624519 | TTAGTCTAAGCCATG[C/T]TCATCTCTTACCTGG | 5521 |
rs73318507 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045775 | TCATCTCCACTGTAC[C/T]CCATCTTGGTCTCTG | 5521 |
rs73318524 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059340 | AATGAAAAGAAACAC[C/T]TCCTGTTAAAAGGCA | 5521 |
rs73320012 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691735 | CACCTTTCTGACCCC[C/G]CTGTCCATCCTCTCC | 5521 |
rs73320028 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699649 | TCTTTATCATCACTG[C/T]GAACTTAATTGGTTT | 5521 |
rs73320030 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700022 | ATTTATATGGAACCC[C/T]GAGGGATTACGATGC | 5521 |
rs73320035 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702327 | GAAAAGGCTCCTTAT[G/T]GTCATTCATTGTGCA | 5521 |
rs73320038 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704411 | GTTCAACATGGCTTT[C/T]ACCTTTAAATTGTAA | 5521 |
rs73320040 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705808 | TACTGGGATTATGCC[A/G]AGATGACCTTGTTGA | 5521 |
rs73320045 | snp | A/G | 0.380919 | 0.21298 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707624 | GGAGTGGAGGCAGGC[A/G]GGCTGAACCAGGCGG | 5521 |
rs73320051 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711816 | GAGGTTGGGATACAA[G/T]TACAATGTTGGGGAA | 5521 |
rs73320055 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712112 | CGATGTCAAACAAAA[G/T]AAATATGTTGCTAAT | 5521 |
rs73320067 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724327 | TAGGTTTTTTTTTTT[A/G]AGGGTTACATGAGAA | 5521 |
rs73320075 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732564 | CCTGGAAGTGAATTC[C/T]AGTTGAAACCATGCT | 5521 |
rs73320076 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732910 | ACAGTTAATGAAGGA[A/G]GCTGATTCTAAAGCC | 5521 |
rs73320081 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735590 | GGGAAAAAAAGAGTC[C/T]CACACTCAGGTATAA | 5521 |
rs73320084 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737490 | AGAGCATGATTCAAC[A/C]AATATCTATGGAATC | 5521 |
rs73320100 | snp | G/T | 0.0267878 | 0.112589 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741883 | TCGATATTAGCCTAG[G/T]ATCCAAATATAAACA | 5521 |
rs73320102 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743610 | TCCTTGAGCACTAAG[C/G]CTCTATATGCTTTAA | 5521 |
rs73322105 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745271 | GGGCCTGAGTTCTTA[C/T]CCTAGTTCTACCACT | 5521 |
rs73322106 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745371 | ATTTTGAGATTTTTG[G/T]CCATAAAAATGGGAT | 5521 |
rs73322109 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745554 | GCACAATTATTAGAG[C/T]CCTCTAGATTGGTAA | 5521 |
rs73322118 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762225 | TTTACTGCAGAATAT[A/G]GAATAATCTTTCATA | 5521 |
rs73322121 | snp | C/T | 0.0422008 | 0.138995 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767781 | TTAGGGTTCACTCTT[C/T]GCATTGCACATTCCA | 5521 |
rs73322122 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768997 | ATTCTCCTGCCTCAG[A/C]CTCCCAAGTAGGTGG | 5521 |
rs73322133 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781388 | CTGTATCCTTGAAGA[A/G]GGCAACTTGAATATT | 5521 |
rs73322136 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785276 | AGCTGGCCAGGCACC[A/G]TGTCTCATGCCTGTA | 5521 |
rs73322143 | snp | G/T | 0.110519 | 0.207473 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787265 | TACATGATCTACAGG[G/T]TGATCACTATTGGCC | 5521 |
rs73322151 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801145 | AAACATAAAAACAGA[A/G]TAGGATAGCAGTTAC | 5521 |
rs73793203 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594852 | TGAAAGCAGAGGGAG[C/G]CTACCAAGGGCATTG | 5521 |
rs73793208 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633844 | TCCCTGGGCTCTCCC[C/T]GTCTGCTTCTCCATC | 5521 |
rs73793209 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634784 | CACACACACACACAC[A/C]CCCTACTGGTTCTGT | 5521 |
rs73793212 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667530 | AGTAATATTCTAGTC[G/T]GGGCTCTTTAGATTT | 5521 |
rs73793214 | snp | A/G | 0.249603 | 0.25 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674554 | TGGGTCTGTTCATAT[A/G]TTTCCCTTCTGGTCC | 5521 |
rs73793215 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677402 | AATGTTAGGCAGGGG[C/T]AAATGAAGTACATGC | 5521 |
rs73793217 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683389 | AGTCATAAAGACGTG[A/C]ACTCAAGTCCAAGCA | 5521 |
rs73793230 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719976 | ATTTACTGCACCTCC[C/T]AACATTTCCTAGTGT | 5521 |
rs73793232 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728390 | TAAGCAGCAAAAACA[C/T]TGAATAGGTGTGTTT | 5521 |
rs73793241 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742431 | TGTTCTGGATCCTTT[C/T]ACCTGAAACATTAAT | 5521 |
rs73793243 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743822 | ATATGGCCACAAAAT[C/T]ATTGAGCAAATATTG | 5521 |
rs73793244 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744095 | ACATACTAACTTACA[A/C]ATATATCTTTAAAGT | 5521 |
rs73793245 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744144 | TCCTCCTTTTCATAA[C/T]ATTTAAAAATCTGAA | 5521 |
rs73793246 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744818 | TCTTATTCTGCCTAG[C/T]CAGCTAAGATATTTA | 5521 |
rs73793251 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748173 | TAACCTGAGGCCCCA[A/T]GAGGCTGCCCATGGT | 5521 |
rs73793254 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753516 | GAACTAGGCCAGTTC[C/T]TTTTGTCAGCTGTCT | 5521 |
rs73793256 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753622 | TGAATGTAAGGAATT[C/T]GGTCTGATGCTCGGT | 5521 |
rs73793257 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754762 | GAACCCTGTGGAGAA[C/G]CCCATGTGGCAGCCT | 5521 |
rs73793259 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755400 | ATTTAATAATAAACA[A/G]GGTTATCAGCGGAGC | 5521 |
rs73793260 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761759 | CAATAAGATGGAAAA[C/T]AATAATTACAGTATG | 5521 |
rs73793263 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766656 | TGAGAAAACAGGCTC[A/C]GAGAGGTTAAGTTCT | 5521 |
rs73793264 | snp | A/G | 0.0850919 | 0.187897 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769593 | ATGAATGAATGACAC[A/G]GAACATATCTTGGAA | 5521 |
rs73793265 | snp | C/G | 0.0850919 | 0.187897 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769605 | CACGGAACATATCTT[C/G]GAAAATACTGCTTTA | 5521 |
rs73793266 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772120 | ATCCATACTAAAAAA[C/T]ATAATGCAACCTTTA | 5521 |
rs73793268 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772935 | TCTTTTGTTACTAAG[A/G]CTCCTCTGCCTGTAA | 5521 |
rs73793269 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773262 | CCATACTGCACAGCC[A/G]TTTGCATTCCAGGAA | 5521 |
rs73793272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777743 | TTTTTCTATGCACAA[C/T]TGAGAAAAGGAAAAG | 5521 |
rs73793273 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779052 | AACAACAACAAAAAT[A/G]CCATTTGATTCGTGG | 5521 |
rs73793274 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781183 | ATATATATAAAATTA[G/T]TCTCATGATATAAGT | 5521 |
rs73793279 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814018 | ACTTGAAGAATATCA[A/G]TAAGGCAGTGGATTG | 5521 |
rs73793280 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814898 | ACTTTCCTTCCTTTC[A/G]CCCCTGCCTTGGTCT | 5521 |
rs73793281 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815554 | ACGCAAGTGAAATAC[G/T]TAAGAGGAAGGGCGT | 5521 |
rs73793283 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817049 | ATGAGCGTTGCTCTT[A/G]AGGGCTACTCCCCTC | 5521 |
rs73793284 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818209 | AAATTTTAAACTCTA[C/T]GAGGGCATGGAAAGC | 5521 |
rs73793285 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818478 | AAGATGTCCCCATCC[C/T]TGCCCCAAGATTTAT | 5521 |
rs73793286 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822462 | CTCTCCACATTCATT[A/T]CTGCTCCAGGGCCTT | 5521 |
rs73793288 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823976 | TCCCTCCTGGATCCC[C/T]GGTAGTAGATGTGCA | 5521 |
rs73793290 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824163 | TCAAATCTGATGGCA[A/G]CATAATTTACTGAAG | 5521 |
rs73793291 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824312 | TCACAGGGAAGATGT[C/T]CACATTGGTAGTGAG | 5521 |
rs73793292 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824587 | AGGGAGTATGCACTA[A/G]AAAAAGTAGACTCAT | 5521 |
rs73793293 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825596 | TAAAGAAATACTTAT[A/G]GATGGATTGAAATAA | 5521 |
rs73793294 | snp | G/T | 0.0528381 | 0.153711 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825918 | AATAATTGAAGTTTT[G/T]GTTGTCTCCTCCAAT | 5521 |
rs73793295 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827824 | TCCTTTAATTCTGTC[A/G]GTAAATACTGGGAAG | 5521 |
rs73793300 | snp | A/G | 0.122758 | 0.215196 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847554 | ATCTCCTGGCCTCCA[A/G]GAACCCACCACAGGG | 5521 |
rs73793305 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911808 | GTCAAGTGCCTAGAA[C/T]GTGTAGCACACTAGG | 5521 |
rs73793312 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958201 | AGGCACCATCTATGA[A/G]GAGAAGTACCTTTTA | 5521 |
rs73793313 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967662 | AACCTCAGGGGCAGC[C/G]CCACTCAGTAAAGCA | 5521 |
rs73793319 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000693 | AAAACCACAATTACT[A/T]TTGCACCAACCTAAT | 5521 |
rs73793320 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023706 | CAGATAGCTGGTGAA[A/T]CATTATTTCTGAGTG | 5521 |
rs73793323 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056679 | AATGAGAGAGAGAGA[A/G]AAAAAGAGAGACAGA | 5521 |
rs73793325 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074396 | CCCTGTATTCAGGAG[C/T]GGGAAGAGCAAGGCA | 5521 |
rs73796003 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852133 | CAGAGAAAGGGGACC[A/G]ATAACAGCATCCTCT | 5521 |
rs73796004 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855434 | ACACATCTTTATCCA[G/T]AGTCTGATGGAGAAT | 5521 |
rs73796005 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858200 | TAGCAAGTGGTGGAG[C/G]CAGGATACAAACCCA | 5521 |
rs73796023 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889528 | ATGCATATTGTCACA[C/T]GGCAGGAGGTTAATG | 5521 |
rs73796024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890029 | TCCCATGATCACATC[C/T]GCACACACACAATGG | 5521 |
rs73796025 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890786 | ACCCAAGTTTATAAA[A/T]TTACAATTGAAAAGT | 5521 |
rs73796027 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890864 | TTTTGAGAATTTAAT[A/G]ATTTCTCTCCCCAGG | 5521 |
rs73796029 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892469 | CATGCACACATGCAC[A/G]TGAGCACCTCTCTGT | 5521 |
rs73796035 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895457 | TTTTTATTCACTATT[A/G]GATTCCCAGTGCCTA | 5521 |
rs73796036 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895757 | TGGCTTCTCTTGAAA[C/T]AAATGTCAAAAGAAT | 5521 |
rs73796037 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897344 | CTTCTCATCACACCC[C/T]GGGTGGATACAATAA | 5521 |
rs73796039 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897565 | ACAGTTCTACTGATT[A/C]ATTCTCACATATGAC | 5521 |
rs73796041 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900364 | TACAATGTAGAAACA[C/G]GGAGAACCATCCACT | 5521 |
rs73796042 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900485 | TTCCAGCTTCCCTTC[C/T]TTTTCTTTCCTTTCT | 5521 |
rs73796092 | snp | A/C/G | 0.0693013 | 0.172766 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909681 | CTGTGTTGCAAGCCC[A/C/G]CATGTCCTCTGTGTC | 5521 |
rs73796093 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909900 | ACAGATTAAGGACTA[C/T]CCCTATGGCTAATTT | 5521 |
rs74293355 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858033 | TAACATTTAGCAATT[A/C]CTACCTACTATTTTC | 5521 |
rs74334957 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681613 | CTTCCTTTGAAAAGT[A/T]TACAGAGAGCCCTTT | 5521 |
rs74335956 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648104 | AGCCAGACTACATTT[C/T]CTAGGCTGCCTTGCA | 5521 |
rs74356729 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597794 | AAAGAAAACACCTAC[A/G]TGTTCCCATCACAAA | 5521 |
rs74357413 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676309 | ATTGCTCATGGGGAA[A/G]AAAGCGAGTTCCTTA | 5521 |
rs74358288 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750520 | TTTAAGAACATGCAG[C/G]CTTCTTGTGATAGTA | 5521 |
rs74358357 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842488 | TCCATGCCCTTTTTT[A/T]TTTTTTTTTTTAAAG | 5521 |
rs74375038 | snp | A/T | 0.47614 | 0.106587 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012279 | ttggtctattcagag[A/T]ttcaacttcttcctg | 5521 |
rs74376483 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812264 | AAAGGTATAAGAACT[A/G]TACACATGGATGGTA | 5521 |
rs74376619 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594915 | TTTTTCCTGCAACTG[C/T]GGCTCTTTCTCTTCC | 5521 |
rs74382744 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752094 | TGGTGGATAGAAATC[G/T]GTTACAAGTTTATTA | 5521 |
rs74387250 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634986 | GTTGGGGTTTCGAAC[A/T]TCTTATGTCTGCAGG | 5521 |
rs74388475 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063902 | AGTAAGTGGTTTTAA[C/T]GTCTTTTCAAGAAAA | 5521 |
rs74388501 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658636 | TAACTTCCATGTTCT[C/T]CTTCCTAAAATCAGA | 5521 |
rs74392648 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707844 | TCTCTATAGACAAAA[A/G/T]TTTATCAGAGAGAAT | 5521 |
rs74410309 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023628 | TGCCAGGGCCAAAAT[A/G]GGACAATTCATACTA | 5521 |
rs74412654 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988019 | AAATAATTTTAAGAG[A/G]CAAAATGCTACTATG | 5521 |
rs74425561 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687794 | GCTGAGTCTCTCAGC[A/G]CTGAAACAGAACAGG | 5521 |
rs74449263 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980506 | CAGAGCTGGAAGAAA[C/G]AGCAACAAGGAAAAG | 5521 |
rs74460028 | snp | A/G | 0.164546 | 0.234942 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756105 | AGGAACAAACCAGAG[A/G]CATTTCCTTCTCTTG | 5521 |
rs74460118 | in-del | -/AA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745973 | AAAGAAAAAAAAAAA[-/AA]GATAAATTGTCCTAG | 5521 |
rs74463018 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870035 | CAATATTCCCTATTA[C/G]AGACATTTACAGCTT | 5521 |
rs74469429 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052055 | GGTCCACAGAGAAGG[A/G]AAGACAGTCCAATCC | 5521 |
rs74472521 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747967 | AAGCATGGTTTAACC[C/T]GAGATGTTCCAGGGC | 5521 |
rs74489779 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652390 | ACAAAGTCCTGGAGT[A/G]TTCAACTGGTAAGCA | 5521 |
rs74491766 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993118 | CAGCTAATTTTTGCA[A/T]TTTTAGTAGAGACAG | 5521 |
rs74500684 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677864 | AAAGATTCCTAGTCA[C/G]TGGATTACAAGCCCC | 5521 |
rs74503244 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954996 | ATGATGAATAACTTA[C/T]CTGCTCGATGGTCCT | 5521 |
rs74514939 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958963 | TAGTAAGTAGTTGGA[A/G]GTGGGATTCAAACAA | 5521 |
rs74516470 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604798 | AGCTAGGCAGTGGTA[A/G]AGATGGGCTCTTGAC | 5521 |
rs74518118 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888954 | TCACTCTCTATCCCT[A/G]TATTGCAACTAGACT | 5521 |
rs74525980 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022400 | TGTCTCTGCTAAAAT[A/T]AAAAAAAAAAAATTG | 5521 |
rs74531731 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847253 | TTGTCCACTAACCCC[A/G]GGATAAAGTTCAAAT | 5521 |
rs74548479 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980450 | CATCCAGAAGGGAAA[C/T]CTGATCACTGACAAC | 5521 |
rs74550911 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808293 | AGGGCTCAACAGTCA[C/T]ATGTGCCTAGCGGCT | 5521 |
rs74552500 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910503 | GTGCCATATGATTGT[C/T]GCTTCCTTTACTCTA | 5521 |
rs74560425 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906991 | TGAGTAACACAGGAA[C/G]GGGGCGCTGCAGGGA | 5521 |
rs74573750 | snp | C/T | 0.0441095 | 0.141807 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866639 | ACATACATATATATA[C/T]ACACACATATATATG | 5521 |
rs74580118 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076814 | TTCTTGAGAGCTTGG[A/G]CTATATTTGATTTAT | 5521 |
rs74584411 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604708 | AAACTTCTAAGGAAG[A/G]TACTATCACTCTTCT | 5521 |
rs74586166 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717217 | AATCTAGTACCAAGG[C/T]CATTTTCAGAAATGC | 5521 |
rs74588621 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673529 | ATAAAGTCTAATATT[C/T]GATAGTGGATCCTTT | 5521 |
rs74598525 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698691 | GATATTAAATGACTT[C/T]CCCTAGGTCTCACAG | 5521 |
rs74617542 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742896 | AGGCAGAGATGGGGT[A/G]ATGCATCTGCAAGCC | 5521 |
rs74620048 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722039 | TGTCATTATTACTAC[C/G]CCCATTTTACAGATG | 5521 |
rs74638964 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884109 | TTTTTTTTTTTTTTT[G/T]TTTGAGAGCCAGTTG | 5521 |
rs74641114 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852186 | GCAGGCTTATGAGGG[A/G]ACAGGAAGCTGGGAG | 5521 |
rs74664312 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673111 | CATCTGTCTGAGTTA[C/T]GGTTTTTTCCTTCTG | 5521 |
rs74666462 | snp | A/C/T | 0.00518141 | 0.0506816 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790113 | TAGTTAATTGCCCTT[A/C/T]GGGACTGCTCTGTGT | 5521 |
rs74670292 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983657 | CTATTTTAAACTTCT[C/T]TTCTACATAAATTTA | 5521 |
rs74675837 | snp | A/T | 0.0944967 | 0.195752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969000 | AAACAATTCAGGACG[A/T]TTAACAAGTGGCGCC | 5521 |
rs74679375 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607214 | GCCAACAATTTTCCC[A/G]CAGAGGGTAAGAACT | 5521 |
rs74679926 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641606 | TTTGGTGAGTTCTAG[A/G]AACATTTGAGAGAAG | 5521 |
rs74686802 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719110 | TGAGAAATAATTCTA[A/G]GAGTTGATCAATAGC | 5521 |
rs74693963 | snp | C/T | 0.079617 | 0.182947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027893 | TGGTGCTTAAGTGTC[C/T]CTTTTGGGCGATGAG | 5521 |
rs74695109 | snp | A/C | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976889 | TTCCTACCCATCACT[A/C]CCATAAAACTAACAA | 5521 |
rs74702040 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851790 | AAGATGCATATCTCA[A/G]CAGAGCAGCTGTTTC | 5521 |
rs74705683 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619619 | TTCATGTTAGCAACT[A/G]ACTAAAGAAACTTGA | 5521 |
rs74707628 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688978 | AATATATTGCCAGTA[C/T]GGTGTTTGCCACTTA | 5521 |
rs74722610 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929171 | TCCACATCCCTCTCA[C/T]TCATTCCCACATTTC | 5521 |
rs74723097 | snp | A/C/G | 0.0376468 | 0.132172 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922815 | ACTCAGTTCAGGCCA[A/C/G]TGAGAAACAAGGAGG | 5521 |
rs74735371 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976042 | TATCCAAGAAATCAT[G/T]GCCAAATTCAATGTC | 5521 |
rs74737268 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813243 | AATCATTAAAAAAAA[A/C]CCCTCTCTTTACACA | 5521 |
rs74739055 | snp | C/G | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676421 | CTCAGCTTCAGCCAC[C/G]TGGGCCCTCCTTCCA | 5521 |
rs74740010 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796264 | ATGCTCCCATACGTC[A/C]AAGTGTATACATATC | 5521 |
rs74750465 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074037 | TGAGGCTCTGTCTCA[A/C]AAAAAAAAAAAAAGA | 5521 |
rs74751699 | snp | A/T | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621383 | GCAGAGCTAGGACGT[A/T]AACCCAACTCTGGCT | 5521 |
rs74755236 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790363 | AAAAAGCCCTTTGCT[C/G]TTGGGACCTTAAGTG | 5521 |
rs74756015 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804799 | ATCAAAGAGGAGCAG[A/G]TCGCCTGAGGAGAAG | 5521 |
rs74769731 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642320 | GAGCCACAAATGGTT[C/T]ATCAGTGTGGGATGA | 5521 |
rs74771279 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701596 | CTTGAAGCTTAGACA[C/T]GGAAAATGGAGGAAC | 5521 |
rs74774435 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059156 | ATACCACCCCTGCTC[C/T]AAAGAAGTGCATATT | 5521 |
rs74793005 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850852 | GTATACAATAAGTGC[C/T]CAATAAACACCTATC | 5521 |
rs74801548 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985038 | TTTTTTTTTTTTTTT[-/TG]AGACGGAGTCTCACT | 5521 |
rs74808740 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005606 | TGTACTGCTGTTCTC[C/T]CTTCTCCTTTCCCTT | 5521 |
rs74812438 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800017 | CACGATAGTTCATTA[C/G]TGGGTGTGGAATCGA | 5521 |
rs74819327 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048435 | AATATTTTTGAGAGA[C/T]AGTAACTGTGAAGTA | 5521 |
rs74819889 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769383 | AGCCCTTCAGGTGAT[C/T]CTGATACAGGCTAAA | 5521 |
rs74869864 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775303 | ACACCCTGAGCAAGT[A/G]AAATTTATCCCAGGA | 5521 |
rs74871617 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071626 | TCCTCCCCAGATATT[C/G]ACAAGACGATATTTT | 5521 |
rs74879916 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008962 | TAGATTGCACCGTTT[C/G]GGCCTCTTTACTGAT | 5521 |
rs74887084 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040334 | TGCCTCACCTATAGG[A/T]TCACTTCCATTTATC | 5521 |
rs74891498 | snp | C/T | 0.221439 | 0.248363 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657159 | CCCCTGAAGCCTCCA[C/T]TTTAAAAAACATATG | 5521 |
rs74892356 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830286 | GTAAACTAAATAATT[A/T]AAGCCACACGTTTAA | 5521 |
rs74893595 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604168 | AATGTGGTTACAGTT[C/G]TGAATAAGTGTGATT | 5521 |
rs74900892 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925285 | ATAGAGTACCATTTC[C/T]GGAAGGCCTTCCTTC | 5521 |
rs74904408 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078809 | CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 5521 |
rs74908975 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652369 | ACAATATTTACTGAG[G/T]GCCACACAAAGTCCT | 5521 |
rs74911745 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746950 | CATTCGGGTCTCTTG[G/T]CTCCAAGGCTTTTCT | 5521 |
rs74912536 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686518 | TATTAAGGATATAAA[A/T]TCTAGTACCTGGCAC | 5521 |
rs74913470 | snp | G/T | 0.078151 | 0.181571 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030081 | TTGCTGTATATCACC[G/T]AGGAAAGAATAAACA | 5521 |
rs74918872 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923139 | CTTTTTTTGTTTAGC[C/T]GGTTTTGAGCCAGAT | 5521 |
rs74940539 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908202 | CACTTCTGTGATACA[C/T]CATGCAAAATATTAG | 5521 |
rs74951391 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680562 | ATAATAATAAAAAAA[A/C]CCACAGCGTTGCACA | 5521 |
rs74955406 | snp | C/G | 0.206111 | 0.246117 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920820 | CTGCAGTATCCCCTA[C/G]GTTTGAAAAACAGGT | 5521 |
rs74986640 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877012 | ATTGTCCTAAAGCAT[C/T]TCCACATACATTTTC | 5521 |
rs74990018 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779985 | CACTAAATTAGGTAG[C/T]TTTTTCTGTATTCCA | 5521 |
rs74993396 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835949 | TTAAGCTATGGGACC[A/G]ATTATGAAACTTTCC | 5521 |
rs74993429 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796260 | ACGTATGCTCCCATA[C/T]GTCCAAGTGTATACA | 5521 |
rs74994441 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811471 | TTGCTATCCTAATGC[A/G]CATTAAACTTTATAG | 5521 |
rs74995456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594148 | TCTACATGTGGAGCT[A/G]TCGAGTAGACTCTGA | 5521 |
rs74999186 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786497 | CTGTACCCACCTGGG[C/G]CTCCTGACAACCACC | 5521 |
rs75010121 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698853 | CCTCTTGGCTTTCCT[C/G]TAGCGCTGATTATGC | 5521 |
rs75014008 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780663 | CTGTTGAATATATAA[A/C]ATAAAAAGAAAACTA | 5521 |
rs75014122 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598789 | TAAGCTACTATTGCC[A/G]CTTGCCAGAATGTTA | 5521 |
rs75019045 | in-del | -/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698746 | AGATATGCCCCTGCT[-/TTT]CCTTTTTTTTTTTTT | 5521 |
rs75032123 | snp | A/G | 0.040671 | 0.13668 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955112 | AGAGTGAAAACCATA[A/G]TTTAAACATAAGCAG | 5521 |
rs75043865 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003001 | ACTACAGCCTGACCC[C/T]AATATTCTCTCTCTG | 5521 |
rs75050220 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978773 | TTTTGGTTACTGCAG[C/G]CTTGTAGTATAGTTT | 5521 |
rs75099369 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908673 | GTGATGACCTAGAGT[A/G]TTGAGAAACTTCCCA | 5521 |
rs75123014 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662390 | TTAGAAACAAATTGA[C/G]TTAAGATTGACATTT | 5521 |
rs75132174 | snp | A/C/G | 0.0260207 | 0.111123 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941227 | CTTTCTTCTCCCCAA[A/C/G]AAATGCCATATGTCT | 5521 |
rs75136342 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740908 | GAACACATTAAAAAT[A/G]CAGATTCCATCCCAG | 5521 |
rs75137671 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794012 | TTCATTTTGACACAT[A/G]TCTCAGGAAATTCTG | 5521 |
rs75160803 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857416 | TAGTCCATTATTGTT[A/C]ATTTTTTAGTATCTT | 5521 |
rs75168890 | snp | C/G | 0.0495547 | 0.149404 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055175 | TCTGTAACCCAAGTA[C/G]AGACTCCAAGTGAAC | 5521 |
rs75175331 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926256 | GATATTTTTTTTCCC[A/T]TTATGGTGGTTGTTG | 5521 |
rs75192875 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792540 | TAAGTAAGGTATGTA[C/G]TATGTTAGAAGGTGA | 5521 |
rs75203908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598116 | GTCCTCATAATGTTC[C/T]CATCTTCAGTTTCTT | 5521 |
rs75208747 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702842 | CTAGTTCATTTTCTC[A/G]AGAAGACTCCAGTGA | 5521 |
rs75227806 | snp | A/C/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676916 | TATCTAATTGGGACT[A/C/G]GTGTGGCGGTCACCT | 5521 |
rs75228899 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966471 | GTATTCTTACACTGC[A/G]GCTATGTGAGCAGAG | 5521 |
rs75232318 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872593 | TTGGAATGGGGGATG[C/G]AGGAGGAATCTTTAC | 5521 |
rs75236264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676881 | CTTAATTGGTTTGAC[C/T]GTCAAGTAGTGCAAC | 5521 |
rs75240479 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591976 | TGTAATTTTTGAATC[A/G]AGGCTAAGATAGAGG | 5521 |
rs75243703 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675440 | ACTGTGGGATAGCAG[A/G]TTAGTTGCAATTGGT | 5521 |
rs75247693 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768903 | CTTTTTTTTTTTTTT[G/T]AGACAGTCTCTCACT | 5521 |
rs75253212 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072112 | GGTCTCTATAAGACA[C/T]TGGACAATTTAAAAC | 5521 |
rs75255627 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984230 | AGACTTTGTATGCTC[G/T]GACTATCATCTTCTC | 5521 |
rs75263747 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629286 | CTTCCCCAGTCTCCT[C/T]GTTTCAGTGTATGGT | 5521 |
rs75286513 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011429 | CTATATATAACTATA[C/T]AACTAACTATATAAC | 5521 |
rs75288922 | snp | C/G | 0.0414363 | 0.137845 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620037 | CCTGCCGGGCACCAT[C/G]TAGGGTAAGAATTAT | 5521 |
rs75299512 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929380 | AAACATCTGTTGAAC[A/G]AACAAGTCAGCAGTG | 5521 |
rs75301940 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051781 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCATT | 5521 |
rs75303385 | snp | C/G | 0.0505692 | 0.150756 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607695 | TTTTCTTTTCCCAGA[C/G]AGGAAAAACAGACCA | 5521 |
rs75321158 | in-del | -/AAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027655 | AAAAAAAAAAATTTA[-/AAA]GTGTGGATGGCTAAG | 5521 |
rs75323848 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800019 | CGATAGTTCATTAGT[A/G]GGTGTGGAATCGATC | 5521 |
rs75335036 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867153 | ACTTGACAAAGCATT[A/G]TCAAATTAAAAGTAG | 5521 |
rs75348091 | in-del | -/AT/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844378 | AAACATTAAAAAAAA[-/AT/T]ATATATACTGAAACA | 5521 |
rs75353257 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733907 | TGGTAGTAATAGTAG[A/G]CAATAATAACGGCAG | 5521 |
rs75353760 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864419 | AAAAAAAAAAAAAAA[A/G]AAAGCACAGCTTTCC | 5521 |
rs75355099 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039575 | ACCAGTAAGCACCCA[A/G]ATTAGCCACAACTGC | 5521 |
rs75361530 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821318 | AAGGCTATTTTTATC[G/T]TCTGAGACCTCCTTT | 5521 |
rs75364147 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680594 | ACTTAAAAAAAAAAA[G/T]TTCCCAGAAATCCTG | 5521 |
rs75372385 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071338 | TCAACCGATTCCTGC[C/T]TCTGACAGTGGTCCC | 5521 |
rs75376175 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915850 | AGACAAAAAAAATCA[A/G]TTTCAACACTGTTAC | 5521 |
rs75377541 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621713 | GACATGCCATTAACA[A/C/T]GTGGGCTATCCTTCC | 5521 |
rs75377909 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936843 | CTTGTTCTGTTGTGG[A/G]AGACAAACCAGTGAG | 5521 |
rs75392963 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077514 | TTTATTGACTTTGAG[C/T]GTATAGAAAATTAGG | 5521 |
rs75399437 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072576 | CTCAATTTCCTCCAC[C/T]GTAAAATGGGCTTAA | 5521 |
rs75403035 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631086 | GAAACAAAACAAAAT[C/T]GTCCTGGGCTGTGCT | 5521 |
rs75419449 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656902 | CTCACCCGCTTTGAG[G/T]CTTCCTCCCTCAGGT | 5521 |
rs75426067 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594601 | TGATGTAGGTACTTT[A/C]ATTCTCTTTACTTTA | 5521 |
rs75437888 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833813 | TTACTGATCCCCTCA[G/T]CCCCTAACAATCAAT | 5521 |
rs75439076 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908049 | AGCCACGTTCTTTAC[A/G]TTAATTCTCACGTTT | 5521 |
rs75439784 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606019 | AAATAAGGTTCCAGA[A/T]TCTGGGGAAAATCTT | 5521 |
rs75446335 | snp | C/G | 0.0182389 | 0.0940315 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875296 | TAAAAGAGGAGGAAA[C/G]GTAGGGGAGGGTGGT | 5521 |
rs75449399 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724217 | TCCCACATGATTTCA[A/G]ATCCAGGTTTTGCAA | 5521 |
rs75450474 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673901 | CACTTGCAGTTTCCC[A/C]TTCTCAGGGGAATTT | 5521 |
rs75451813 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644264 | AAAAAAAAAAAAAAA[A/G]AAGAAGAAAGATTCT | 5521 |
rs75453143 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604050 | GATACGTGCCAGGCC[C/G]TGTACCAAATGCTAA | 5521 |
rs75456591 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060748 | AGCTGCTGTGAGGAT[C/T]AAATGAGGTAATCCA | 5521 |
rs75461620 | snp | C/T | 0.0263992 | 0.111815 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919528 | ATTCTGAGAGAGATG[C/T]TGCCCAGGCAACAAA | 5521 |
rs75481845 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638930 | TGATGATAATAATAA[C/T]AGCTGCCACCAATAA | 5521 |
rs75504659 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071943 | GGAGCTGAAAGCATC[G/T]TGAAAGCATGATGGA | 5521 |
rs75518081 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920515 | GGGCAGTAACAATAT[A/G]CCACCTGATTGCTTT | 5521 |
rs75534213 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807225 | TTCTATAATTATACT[A/G]TAAGTGGTCCAGTGT | 5521 |
rs75562149 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636775 | ATATGAACCATCATT[A/G]CTATTTAACCTCATT | 5521 |
rs75564869 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727421 | GGATTAAATAAAGCT[A/G]ATTAACATAACTATC | 5521 |
rs75565236 | snp | A/C/T | 0.0240643 | 0.107019 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858363 | AACAACCAACTACTC[A/C/T]CTGAATGTTTAATCT | 5521 |
rs75571987 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623789 | GTCTGTGCTTGATAA[C/T]GATGGAAGGCCAGCA | 5521 |
rs75584399 | snp | G/T | 0.079617 | 0.182947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037205 | AATCACAGCAACAGG[G/T]GCTGTGGAACCAATT | 5521 |
rs75592648 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941788 | AATAGCTTTTGTGTT[G/T]GTTTCTTAGGGCTGC | 5521 |
rs75599143 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608984 | ATATATCAAGAGAAC[G/T]ATAAGCCAATATCCC | 5521 |
rs75601738 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644776 | AAACAAGATAATGGA[A/G]AAGATAATTTAAGTG | 5521 |
rs75641010 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593512 | TAAATAAATAAGATG[A/T]TTAGATGGTGATAAA | 5521 |
rs75643681 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745166 | AGAGAAAGACAGAGA[C/G]AGAGAGAGAGAGAGA | 5521 |
rs75645559 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608185 | AGCATGAATAAATGC[A/C]TGGGGTGATCAATGC | 5521 |
rs75646601 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666653 | CTCAACCCATCTCCT[C/T]TCCACTTTCATAGAT | 5521 |
rs75650974 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652145 | AGTGTGTGTGGCAGC[A/G]AATGGGAGACCAGGG | 5521 |
rs75653915 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910774 | TTTAAGAAAATGTAT[A/G]AAATCATATTTTTAA | 5521 |
rs75657735 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689621 | CCATCATTAAGTGAT[A/G]TATGACTGTCATATG | 5521 |
rs75684262 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908040 | CATACCCACAGCCAC[A/G]TTCTTTACATTAATT | 5521 |
rs75717210 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948105 | ATCGTTTCCCTTACC[C/G]TATAAACCCTTAACA | 5521 |
rs75722045 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860189 | ACGTTTTACAGGTCC[A/G]CACAAACAGGTAAAA | 5521 |
rs75799423 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978688 | CCTCAGAAATAACAC[C/T]ACACATCTACAACCA | 5521 |
rs75827361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961805 | CACTGGTCCCCCATG[A/G]AGGAGATTTTTTTTC | 5521 |
rs75828208 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704061 | CTTGTTTTGAACTTT[C/T]ATGTTTCCTGACTCA | 5521 |
rs75834522 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039175 | TGCACCTCTTCAGAG[A/T]TGCCTTCCCTGTCTG | 5521 |
rs75838600 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055450 | GCTTTGAGATTACCT[C/T]TGCAACATTATTCTG | 5521 |
rs75839695 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082800 | GGATACCCATTTGAC[A/G]GTTTGGGCCCTTTAG | 5521 |
rs75855615 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705881 | TAAAACAGTTTATGT[C/T]AAATGATTGCAATTT | 5521 |
rs75888757 | snp | A/G | 0.0310518 | 0.120672 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920268 | ATCATAGTTGCTCCC[A/G]TAATAACTAGTGACA | 5521 |
rs75906333 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901545 | CTCCCCTACATTTCC[A/C]ATGCTATTTCAACCT | 5521 |
rs75959337 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035376 | TCCAATCACCTCCCC[C/G]GAGTTCCCTTCTTCA | 5521 |
rs75968282 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986696 | TTGAAGACAGGCTAT[C/T]TGAAAATACACAGTC | 5521 |
rs75981662 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798834 | TACAGCTAACAAATA[A/G]TAGATCTGGGAATCA | 5521 |
rs75991733 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972418 | CAAGCCCAAACTCAA[C/G]AGGGAGATGTTGGCT | 5521 |
rs75994027 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637165 | TAAGTCTTACCTTTC[C/T]ATTGTACCCCTCAGA | 5521 |
rs76000438 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595098 | AAATTAATTTTCCCC[C/T]ACCTTTACTCTCTCA | 5521 |
rs76001284 | snp | A/G | 0.0414363 | 0.137845 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771741 | TTTCTATTTTTCTTC[A/G]GTATATAGCTAATCT | 5521 |
rs76011640 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687075 | GGGAGTGGTGGGGGG[A/G]GGGAGAGAGAGGGAG | 5521 |
rs76030842 | snp | A/G | 0.000148599 | 0.00861845 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701201 | ACTTTGAAAGGATAG[A/G]TAATAGATATACTTT | 5521 |
rs76034893 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649776 | ATTTTAATTAAACAG[A/G]AGATAATGATACTTA | 5521 |
rs76038095 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602640 | AAAGAACCCAAGTAT[A/G]TAATTAAGTTGCTGA | 5521 |
rs76039069 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615632 | TAATCTCAAGAAATT[A/T]AACCCATTTACAACA | 5521 |
rs76040695 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734924 | TCACTTTTATTACCC[A/G]CCCCTTTCTCTGCCA | 5521 |
rs76050877 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655188 | TGCTTTCAAAGGACG[C/T]ACATCCCAGCACTGT | 5521 |
rs76063740 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951135 | ACTCCAGATTTAAAT[A/G]AAGCATTATTTCTGA | 5521 |
rs76066815 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825336 | GCAGTGGCCCACACT[C/T]CCATGTTTATTTGGA | 5521 |
rs76069075 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957780 | TGGTCTCAGTTTCTA[A/C]GTTGTGCAAAGACCA | 5521 |
rs76070541 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680596 | TTAAAAAAAAAAAGT[A/T]CCCAGAAATCCTGAA | 5521 |
rs76082154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915815 | CCTCCTCCTTGCTAA[C/T]ATTTAAAAATCATTA | 5521 |
rs76090676 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848993 | CTCTTCCAGTTGATT[G/T]CGGTGTCCTTTTGAC | 5521 |
rs76120772 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798172 | TTCTTTTTCATTCAC[C/T]CAGAAGGCAAATTGG | 5521 |
rs76123234 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078255 | GTATTGAGCACTGAC[A/G]CCAATGCTGTATCTG | 5521 |
rs76129136 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895471 | TGGATTCCCAGTGCC[A/T]AAGTACTGACACACA | 5521 |
rs76129666 | snp | C/T | 0.0770498 | 0.180522 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082560 | AAAAAAAAAGAAGAA[C/T]ATTGGCTGAGAAAAT | 5521 |
rs76133379 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870741 | TAAGGGCCCCTCTAG[A/T]TTCCTAAACTCCATA | 5521 |
rs76133928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024571 | ATCATATACTGGGCT[A/G]CAAAGTGAGGCTCAG | 5521 |
rs76134881 | snp | C/T | 0.079617 | 0.182947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040665 | CATGTAACATATACC[C/T]TGGCCCTGAATGACC | 5521 |
rs76171573 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993940 | AGTCATAAACAGGCC[A/C]CAGAGCTGTGTGTGA | 5521 |
rs76191678 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603485 | CACAAGATGGATGTG[A/C]AATGAAAGATGACAA | 5521 |
rs76192236 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602651 | GTATATAATTAAGTT[A/G]CTGAATTAAACCGTG | 5521 |
rs76206792 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705625 | CCTTCTTGGGTCCTG[G/T]ATCACGGTCCAAAGT | 5521 |
rs76209183 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900513 | TCTCCTTTCCTTTCT[C/T]CCTTTCTTTCTCCTT | 5521 |
rs76223143 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777858 | AGTTCTACCTAAACA[C/T]ATTAATCCATGTCTA | 5521 |
rs76225703 | snp | A/C | 0.039522 | 0.134904 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599084 | TTAGTTTATCTCCAG[A/C]ACTTGATCTTTGCTT | 5521 |
rs76264418 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024438 | AATATCAGTAATTAC[A/G]CAGAAGATGCAAACA | 5521 |
rs76275304 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590704 | GCCTCTAAGGCTTCA[C/T]GGCATCAGTGCAGTG | 5521 |
rs76276414 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631152 | GCCTCATCCCAGTAC[C/T]TATGACAGGGGCTGC | 5521 |
rs76280279 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078097 | TAATATTTTTTGTTT[A/G]TTTGCTTGACTTCAA | 5521 |
rs76281801 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791425 | GGTGTGTGCACGTGT[A/G]CGTGTGCGTCTGTAC | 5521 |
rs76284508 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820498 | ACACTCCTTCAGAAA[A/G]CCTCCTGTGTTCAGT | 5521 |
rs76295498 | snp | A/T | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921818 | CATGTCTCACTAGCC[A/T]TTCAAGTATAACAAC | 5521 |
rs76303810 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987728 | GAATAGAGGAGTTAT[A/G]AAACAATCAGAAATC | 5521 |
rs76328257 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937621 | GCTGAGCAGGGGTTG[A/G]CCATGTAAAAGCGTG | 5521 |
rs76331745 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719533 | ATTAAATGAGATAAG[C/G]ATGGGGAGGAGCTTA | 5521 |
rs76334519 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702174 | GAGGTGGAAAACTAA[A/G]GCAATTACCCCTGAG | 5521 |
rs76336632 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730984 | CTCACAGTGGAAAGG[C/G]TTAGAGAGGAAGATT | 5521 |
rs76341467 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699220 | AACTTACTGACCAGT[A/G]AGAGTGCTGAACCCT | 5521 |
rs76347270 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900489 | AGCTTCCCTTCCTTT[C/T]CTTTCCTTTCTCCTT | 5521 |
rs76371672 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080358 | AAGCCCTACTGCATT[A/C]TGCTAGAAGAGCTAA | 5521 |
rs76400336 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643997 | AAGGGTGTGGCTGTG[G/T]TCCAACAAAACTTTA | 5521 |
rs76415477 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943686 | CTCATTTTTTTTTTT[A/T]ATAGCAGAAAGGCAT | 5521 |
rs76419095 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645115 | TAAAGTCTGCCAGTA[C/T]TGAAGGTAGAAAATA | 5521 |
rs76424225 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070244 | TGTTTTCAACACCTA[C/T]TGCCCATATATATTT | 5521 |
rs76428505 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925814 | ACAGGTTTTTGAGGG[C/T]CTGTTAATTTTACTG | 5521 |
rs76433179 | snp | G/T | 0.0633504 | 0.166319 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022008 | AGGAACTTCCGGAGT[G/T]AAAAAATACAGTGTT | 5521 |
rs76442045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056972 | GTCCATAAAAGAAAA[C/G]CAACATTTCCCTGAG | 5521 |
rs76445676 | snp | C/T | 0.117188 | 0.211804 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603363 | GACAACAAAATTGTA[C/T]ATGTTTATGGTGCCT | 5521 |
rs76451926 | snp | C/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920618 | AGTCCCTGCTAGGAA[C/G]TGGCTTTTCATGATG | 5521 |
rs76452609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863924 | TACTTTGAAAGTGGA[C/G]TAAAAATCGCTCACT | 5521 |
rs76453260 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759474 | CATGTTTAGAGTCAG[A/C]CAATCAGCAACAGAA | 5521 |
rs76461274 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639463 | AAATAAACCCCTTCA[C/G]TGGGATGTCTGGCAT | 5521 |
rs76462379 | snp | A/G/T | 0.0528381 | 0.153711 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061552 | TATGTTGTCTTTCTC[A/G/T]CTCATTGCATCCCTT | 5521 |
rs76465341 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686746 | GGCAGCTGATAATAA[C/T]GAGAAAAAGAATACC | 5521 |
rs76476147 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624537 | ATCTCTTACCTGGAG[A/C]ACTTTGATAGCTTTC | 5521 |
rs76504269 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083087 | CAGGTTCTTACCCTA[C/T]CTTGTGAGTTGTCAG | 5521 |
rs76512792 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651032 | TCCATTGTGGAGTCA[C/T]TACCTTCCAGAGACA | 5521 |
rs76515438 | in-del | -/ATG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712969 | TCAATTAAAAATAGA[-/ATG]TAAGATATCTGTCCT | 5521 |
rs76522635 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995236 | TTTCCATAGTAATCA[A/G]TATTCATATTAAGAT | 5521 |
rs76523801 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946590 | AAATTACACTAGAAC[C/T]GTTAGGCCGAAAGAT | 5521 |
rs76526989 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820352 | AAACATTAAAAAATT[A/T]TAAACACACAAAACA | 5521 |
rs76537981 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039576 | CCAGTAAGCACCCAA[A/T]TTAGCCACAACTGCT | 5521 |
rs76546113 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816890 | TAAAAAGACTGTCAG[C/G]TGATTTTGATGAATA | 5521 |
rs76591202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069171 | TAACATTTACAAATT[C/T]CAGTGGTGATCCTGG | 5521 |
rs76599395 | snp | A/C | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017029 | ATTTAAGTTTTGGAT[A/C]GATTGCTCTGGCTGC | 5521 |
rs76620464 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779670 | CTTATAGCTCATAAA[C/T]ATTATAGATGCATGC | 5521 |
rs76630421 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046030 | CATATCCTCTCCACT[A/G]CTGCATTTGTCACAG | 5521 |
rs76632046 | snp | A/G | 0.000557776 | 0.0166906 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054658 | CAGTCTCAGGATTCT[A/G]CCTGGAGGATGAAAA | 5521 |
rs76632388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760017 | CTTAAATAACTTTTG[A/G]GTAACAAGAAAGGTG | 5521 |
rs76633249 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988341 | ACAGCACATGGAACA[C/T]TGTCTAAGATAGAAT | 5521 |
rs76637129 | snp | A/T | 0.0626037 | 0.165477 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022092 | AAAAAAACAATAAAA[A/T]TGAAGATGGGGTATA | 5521 |
rs76638364 | snp | A/G | 0.197393 | 0.244402 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653600 | CCTAAACTCTTCCCC[A/G]GGCCTCCTCAGTTAC | 5521 |
rs76639662 | snp | C/T | 0.14933 | 0.228835 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646780 | TTGTTCTCTCAATAA[C/T]TATCATGATTGTGCT | 5521 |
rs76639694 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925196 | GGAGAAAAAATATAT[G/T]TTATGGAATCTTTTA | 5521 |
rs76641934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958595 | AAAATTTCCATAATG[C/T]AGCCATTATTAAACC | 5521 |
rs76669885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974297 | AGTCCTTTAACATAC[A/G]TTAATTTATATAGCC | 5521 |
rs76675870 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922608 | TAATGGTGGGATAAT[A/G]GGCTTTTGCTAGTTT | 5521 |
rs76677189 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951047 | TCATGATTGAAAGAC[C/T]CAGGCAAATGGCCCT | 5521 |
rs76681182 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802392 | CACTGCCTGGCTTTG[A/G]AAATTTGAGTGCATA | 5521 |
rs76684169 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736872 | TTAGAACCTATAACA[C/T]ACATTTACTCTCTAA | 5521 |
rs76689334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635064 | GTCATTTATTGACTC[C/T]TTTGTGCCTGGCAGA | 5521 |
rs76695007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983593 | CAGTTCTAGTAAACT[A/G]CAGAAATCTTACCTC | 5521 |
rs76708539 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747170 | TCCAGTACCCCATTC[C/T]TAATCATCCTCTGCT | 5521 |
rs76731372 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940286 | CCTGGATGATTGAAG[C/T]GCCACATCTACTTGG | 5521 |
rs76739318 | snp | A/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865361 | TATAGCACATCAAAA[A/T]TGTTTATAATGACTG | 5521 |
rs76748066 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855739 | TCTTAAATCAAAATA[C/T]AGTTCTTTTGTATTA | 5521 |
rs76752255 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755646 | GAAAAAGCCAAGTTA[C/T]ATATTAATGCACTGT | 5521 |
rs76759657 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908476 | ATTTTTTGAACATAC[A/G]TATGTATACAGCTGT | 5521 |
rs76795468 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944949 | TTAACCAAAGATGCC[C/T]TCTTGTAACTTACTG | 5521 |
rs76803542 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979926 | GAGAGCAAAACCATG[A/G]CAGATAAAAGGAGAA | 5521 |
rs76806178 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891695 | TAGTAATTTATGTGC[A/G]AATAAGAGACCAACC | 5521 |
rs76822809 | snp | C/G | 0.0327778 | 0.123752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071157 | ATGACGCCCAGAATT[C/G]TAGCAGTTGTCTTGG | 5521 |
rs76823468 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900539 | TCCTTTCCTTTCCTT[C/T]CTTTTTCCTTCCTTT | 5521 |
rs76832076 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707847 | CTATAGACAAAAGTT[A/T]ATCAGAGAGAATCCA | 5521 |
rs76838537 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602083 | TCTTTGATGCATATA[C/T]CTCATCTACTACATA | 5521 |
rs76874369 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757372 | CATATTTAAAGATAG[C/T]ACTGGCTGCCATGTA | 5521 |
rs76880298 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800030 | TAGTGGGTGTGGAAT[C/T]GATCTGAAAAAAAAC | 5521 |
rs76896552 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982525 | GTTGTTGAGTGTAGG[G/T]TTCTATAAATGTCAA | 5521 |
rs76906150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065743 | TGAGTGTTGAAGGAA[A/G]TTAGGAAGGCAGAGC | 5521 |
rs76934373 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067247 | TTGACTACAGTTACC[A/G]TGTTGTACAGTACAT | 5521 |
rs76936236 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853015 | GTGCTGAGCAGTCGT[C/T]ACAGAGGGGCATGGA | 5521 |
rs76958469 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055946 | TGCCTTACATTTCTG[A/C]ATGCAGCTCAAACTC | 5521 |
rs76962506 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591140 | CATCACACGGTGGTT[C/T]CCCTGGAGTGGGGGG | 5521 |
rs76968235 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705811 | TGGGATTATGCCAAG[A/C]TGACCTTGTTGAAAG | 5521 |
rs76972282 | snp | C/G | 0.0356815 | 0.128715 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916442 | CTTTCCTTCATTCTT[C/G]TTTATCTGTCTTGGT | 5521 |
rs76988578 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765253 | ATCTGAATGCTTTCA[C/G]ATCCCTTAGCTAGAC | 5521 |
rs76989914 | snp | C/G/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925476 | TCTTCTTCCTTCTGG[C/G/T]ATCCATGGTTTTAGA | 5521 |
rs76995085 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732276 | CATTTCTAATGCACA[C/T]ACATTGATAAAAATT | 5521 |
rs77003807 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837144 | AAAGTGATACACATT[C/G]AGTAGAAAATGTACT | 5521 |
rs77012525 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047229 | GGATAAGTTCCAGTG[C/T]TCTATACCACTGTAT | 5521 |
rs77018076 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854285 | GTCAGAAATTCAAGG[A/C]AATTTTTAAAATACA | 5521 |
rs77022175 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768902 | ACTTTTTTTTTTTTT[G/T]GAGACAGTCTCTCAC | 5521 |
rs77031393 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146622234 | GGCCCAATTTTCTCA[A/T]CTGTAACTCCAAGTT | 5521 |
rs77032607 | snp | C/T | 0.000996843 | 0.0223031 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:146856551 | GCTTCATTATTGGGC[C/T]ACTATTCTCTGTCTT | 5521 |
rs77046172 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683054 | TATGGCCGAGAAATA[C/T]GGGTGGGTGTCTTGG | 5521 |
rs77053304 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005587 | TCCTTTCCCTTTTTG[A/G]TGGCTTTGGCAGTGT | 5521 |
rs77053652 | snp | G/T | 0.046775 | 0.145601 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673519 | GAAAATAGACATAAA[G/T]TCTAATATTCGATAG | 5521 |
rs77054758 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947305 | CCTGCATGTGCTTTG[C/T]GCCTACTTCATAATT | 5521 |
rs77062700 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602681 | GAACTAAGCCAAAAC[A/G]TTAATTTTCACAGAA | 5521 |
rs77062986 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682289 | GATGTAATACTACTT[C/T]GAACTTTTCAATATA | 5521 |
rs77065056 | snp | C/G | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823830 | CAAAACATAGCCAAA[C/G]AGAAGTCCCTGTTTG | 5521 |
rs77084424 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601361 | CAGCACTTTGGGAGG[C/T]CTAGGCGGGAAGATC | 5521 |
rs77091403 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737579 | ATTTTAAAGCTTGTA[A/C]TTTTTGATCCATTCC | 5521 |
rs77111274 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050748 | AGCAAATAGTATGCA[A/T]CCTATGTTTTACTTA | 5521 |
rs77116513 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654179 | CCCTGACTCCCTGCC[C/T]CACCCAACTCCAAGG | 5521 |
rs77122994 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686781 | GGCTTACCCTGCAGG[A/G]AGAAGTATGCTAAGT | 5521 |
rs77128556 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712989 | ATATCTGTCCTCATG[C/T]ATCTTACATTCTAGT | 5521 |
rs77129319 | snp | C/G | 0.390277 | 0.206936 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652767 | GAGGCAACACCCCCC[C/G]CCAAAAAGTTTTGCC | 5521 |
rs77144469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989535 | AGATGATAAATTTTA[C/T]TGAATGCTTTTTCAG | 5521 |
rs77148477 | snp | A/G | 0.0388887 | 0.13391 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592933 | AGCCTCTTCAAGACA[A/G]TCTTTGGAAGGTTCT | 5521 |
rs77168793 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849937 | ACTCCAATAGCACAG[A/C]AGAAAAACCAATCTC | 5521 |
rs77180438 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719885 | AGATTGGCAACATCA[A/G]GCTGGCATTCCCATA | 5521 |
rs77184033 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925923 | TGTTGTTGAACTCTC[C/T]AGTGAAAAATTTTAA | 5521 |
rs77200865 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775363 | AATGAGTGTAATATA[C/T]CACATTAATAGAATA | 5521 |
rs77205756 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694781 | ACTAGATAGAGATAC[C/T]TATTATACAAATTTT | 5521 |
rs77225318 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765364 | GGTAAGAAAGTTTCA[C/T]AAGGGCTTTAACAAC | 5521 |
rs77231096 | in-del | -/TC | 0.285519 | 0.247464 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694803 | ACAAATTTTGTGATT[-/TC]TTTTATATTTATGTA | 5521 |
rs77233956 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641589 | TTTTACCTGCTGGAG[A/G]ATTTGGTGAGTTCTA | 5521 |
rs77237335 | snp | A/G | 0.02016 | 0.0983543 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589760 | AAGTGTCCCAAACCT[A/G]TTGGGTTTGACAAAA | 5521 |
rs77249359 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826379 | GATCCCTTATTCTGA[A/T]GTAGAACCTTAGAGA | 5521 |
rs77255134 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058674 | GGCACCTATCTACCC[A/T]CATGCAGAATGGGCA | 5521 |
rs77255155 | snp | C/G | 0.000263912 | 0.0114842 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590248 | GGCAGAGAGCAAAGG[C/G]AATGACATATCTTCA | 5521 |
rs77256260 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949311 | TCAATGGGAAAAAAA[A/T]CTAATAATTTGATTT | 5521 |
rs77266100 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811557 | TAGGATCAACTATGT[A/T]TTTTTTTTTTTTTTT | 5521 |
rs77274811 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075948 | TGTTGTTTAAAATAT[A/T]TTTCTAATTATATTA | 5521 |
rs77277551 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924705 | TTGAATAAGGGACCA[A/T]AACTTTTCATTTTGC | 5521 |
rs77282119 | snp | C/G | 0.330016 | 0.236849 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706358 | TAGCTGAGGCCAGAG[C/G]CTGTGAGGCCCCCAT | 5521 |
rs77296726 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798419 | GATTTTCTCTGTAAT[A/G]CATTCTAAGATGATT | 5521 |
rs77301623 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687402 | CTTGGAGCCTCATTT[A/G]TTAAATGGGCATTTT | 5521 |
rs77306526 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639500 | AGGAGTGGGTTTGTA[C/T]AGATCTCTTCACACC | 5521 |
rs77308282 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591689 | AAAAAAAAAAAAAAA[A/G]AGACTACCAACCTTA | 5521 |
rs77310329 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043248 | ATGGACTAAATTGTG[C/T]CCCCCTGCAAAGTCA | 5521 |
rs77323335 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064686 | AAACAATCTAGCATA[A/T]GAAACAATATTTGTA | 5521 |
rs77333112 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620555 | CTCATATTTGGTCTT[C/T]CACTCTCTGCAAGGT | 5521 |
rs77353780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837213 | ACAGTATTCAATAAG[C/T]TACATGAGCTATTCG | 5521 |
rs77381881 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967527 | TAAACCAGAGCGCTG[C/G]TTTGAACCTAGGCAG | 5521 |
rs77390459 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736354 | TAACTAACAACTGAG[C/T]GTTATGCCCTGCCAC | 5521 |
rs77407323 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606083 | AAAGAATTAAGAAGA[A/G]GACTGCCAACTTTAG | 5521 |
rs77412822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793105 | ATTAGATTCTGGGTA[C/G]ATTTTAAAAATAGAG | 5521 |
rs77414756 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914885 | TTCTCTAGCTCAAAT[A/G]TATCTCCCCTACTAG | 5521 |
rs77416571 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665572 | TATGTCAGCAAGAAG[A/G]TTATTTTGCATTCTT | 5521 |
rs77416864 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808719 | AGAAAGTCCAATCAG[A/G]CAAGTTTTATTTCCT | 5521 |
rs77426210 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913572 | TTTTTTCAAACATCA[C/T]ATTAAAACAGCTCAC | 5521 |
rs77454104 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059149 | ATATGAGATACCACC[A/C]CTGCTCTAAAGAAGT | 5521 |
rs77455402 | in-del | -/GTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983192 | TTTTTTTTTTTTTTT[-/GTTT]TTTTTTGAGACGGAG | 5521 |
rs77458770 | snp | G/T | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923409 | AAGTGTGTTTGACAC[G/T]AGTGAACTGTGTTCG | 5521 |
rs77465118 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663048 | CATAAAGAATTTACT[C/T]TATGCCAGTCACTGT | 5521 |
rs77468404 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618086 | TAGAACCTGTGACCA[A/C]GTTATGTTACATGAC | 5521 |
rs77478847 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913130 | TTCTGAAGGCAAGAA[C/T]GAGTTTATATTCGGC | 5521 |
rs77493205 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024026 | ATTGGCTCCCATCAT[C/T]CTTGGCCTTTGGGCC | 5521 |
rs77549750 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819405 | ACTGGGGTGGGATGG[A/G]AGTATGCAGAGAGAG | 5521 |
rs77553016 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641949 | GCATTGAATTCATGG[C/T]TAATATACAACCCCG | 5521 |
rs77573792 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075419 | ATCTGCATAAGTTAT[A/G]TGATCTCATTCAGTT | 5521 |
rs77579066 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721012 | AATGTTTTAGAGAAA[C/T]AGATAATTTATTTTT | 5521 |
rs77583420 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895928 | TGTCACAGACCAGTC[C/T]GTGATTCTTCAATAA | 5521 |
rs77587078 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685087 | TGCTTAGTACAGTGT[A/G]TAGCATAGTAGACAC | 5521 |
rs77611118 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654867 | ATCCTCCACAGGACC[A/T]GAATGCCCTTTTGCC | 5521 |
rs77612153 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663474 | CCTATAAAAACATCC[A/G]TAAATAACAATATAC | 5521 |
rs77618062 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047348 | TGAGATGATGAATAT[A/G]CTAATTACCCTAATC | 5521 |
rs77618660 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811559 | GGATCAACTATGTAT[A/T]TTTTTTTTTTTTTTT | 5521 |
rs77630919 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838571 | GTGAGCCTCCATCTC[A/C]AAAAAAAAAAAAAGA | 5521 |
rs77648487 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698615 | GCCTTTTAAGATCTC[A/T]CCTGATTCTCATGAA | 5521 |
rs77651511 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826128 | CATTGCCACTTCCTC[A/G]GTACTTGGCATTTCT | 5521 |
rs77652975 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026628 | ACAAATTTAAAAAGT[C/T]ATTTTAAATAGATAA | 5521 |
rs77664831 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742036 | TCTCAGGGGCCAATC[C/T]GTCTGTGTAATGGGC | 5521 |
rs77665418 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683205 | TTTCCCAAAATTAAA[C/T]AGAAAGCCCACCTGT | 5521 |
rs77677854 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768769 | GGCCTCCTCCCAGCT[C/G]TTTCCTGTTCCTGGA | 5521 |
rs77682145 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833702 | AGTGTCAGGCGGGCC[A/G]TGTCTCTTCTTTTTC | 5521 |
rs77686828 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860446 | GACACAGAAAACACA[A/C]CACACTTTCTAAAGC | 5521 |
rs77689741 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635650 | CACTCACTAGAGAGG[C/T]CCTGCCTCCTTAGAC | 5521 |
rs77690228 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599566 | TATCTCCAGGCTCAT[C/T]CTTCTGCCTTTGTGA | 5521 |
rs77694448 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070207 | TTAATACCACAGACC[A/G]TGGCTATTTTGAGGG | 5521 |
rs77696391 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907410 | CCATATGAGCGTTCC[C/T]AAAGTTCAGCTTATA | 5521 |
rs77696842 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924469 | CCCTTCCCAAGTACT[A/G]GAGATTTTAAGTACA | 5521 |
rs77698468 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038960 | ATTTGAGATTATTGA[C/T]TTTTTTTAAACACAA | 5521 |
rs77722012 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643206 | AGAGAGAGAGAGAGA[A/G]GGAGACAGACAAGGG | 5521 |
rs77736908 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073049 | TGTCCTCAGGAAAGT[A/G]TACAGTGCTTAATGG | 5521 |
rs77741221 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635790 | GTCAACCCTTAGGCA[A/C]ACATTTATTAAATAT | 5521 |
rs77782921 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731085 | ACAACACACCAGCTG[A/G]CTCCTTTTCCAATCC | 5521 |
rs77782943 | snp | C/T | 0.107694 | 0.205546 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769760 | CTATAAATACAAACA[C/T]GAGCAAGTCCTTGTT | 5521 |
rs77783934 | snp | C/T | 0.107341 | 0.205301 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780424 | TCCATCCAGGCCCTG[C/T]GGTACGAGGAATACA | 5521 |
rs77785485 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797678 | GGTATTTATTGAACA[G/T]GCAGTAACTGTCTGG | 5521 |
rs77795750 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728949 | ATTGGTACCAGGAGT[A/G]GGGTGTTGCTGAAGA | 5521 |
rs77803965 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835078 | TATGAATAGTCCTGT[A/G]ATGAACAAACAGGTG | 5521 |
rs77806345 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591926 | ATAAAATGATGTGTA[C/T]GAATGTGTTTGGTAT | 5521 |
rs77839193 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066221 | TCCTCTGCCAAAATC[C/T]AGGTATTGGAATATC | 5521 |
rs77840135 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693074 | TCACATGTCCAAGGA[C/T]GGGGATTCCCACTCA | 5521 |
rs77846064 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625620 | GGCATTTAATCCTAT[C/T]TGGGGGTCCAGGAAG | 5521 |
rs77859232 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684406 | TTACGACATAGGTAC[C/T]TCAGAGGGAGCAAGA | 5521 |
rs77861840 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634152 | GAGATTGTACTGCCT[A/G]TTGTCAATGGGCCTC | 5521 |
rs77862502 | snp | C/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921518 | ATCTTTCTCTTACAA[C/G]CTTTTACTGACACTT | 5521 |
rs77862837 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623082 | TGGCCCTTGGAATCT[G/T]CCGGTACTTAATAAC | 5521 |
rs77880940 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811445 | AGATTTGGTTTCTAT[C/T]CTCCTGCCATTTGCT | 5521 |
rs77881554 | snp | A/G | 0.121022 | 0.21416 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000400 | AAGAGAAAAAGCTCC[A/G]GAGCCAAGCTCCCTT | 5521 |
rs77891656 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595536 | AGATAGAAGTTGGGA[A/T]AGATTCAAGGGAAAA | 5521 |
rs77906251 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980995 | AAAAGACTAAATAAA[A/G]AGATATCTACATCTA | 5521 |
rs77913656 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054493 | CAACTGTAAAAAAAA[A/G]GTCCATGAGATATCA | 5521 |
rs77924068 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801602 | GGAAGATACAGGCTG[G/T]GGGGTCAGGCCGCCT | 5521 |
rs77925076 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925681 | ATAGATTAATTTTCT[A/T]AAAAATCAAATTTTG | 5521 |
rs77931113 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783507 | AAGCAATTTAAAATT[C/T]TTCTACTTATGCTTT | 5521 |
rs77941936 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720313 | AAGGGCTGGCCTAAC[C/G]AGTAAGCTGAGCACA | 5521 |
rs77943448 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083478 | GACTTGGTGAATTCA[C/G]TAGGAATAATGTGAC | 5521 |
rs77943633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799977 | CAGGGAAACAGATTA[C/T]GGGAATTGCTCTCCC | 5521 |
rs77947870 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733718 | ACACAGACACACACA[C/G]ACACAAACACACACA | 5521 |
rs77950942 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695747 | AGTTTATCATCGCTT[A/G]TGGCAGCTTTTAAAC | 5521 |
rs77956969 | snp | C/G | 0.0558544 | 0.157504 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690815 | TCATCCCTGTACCTT[C/G]AGTACAGAAGGTGCT | 5521 |
rs77957552 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071837 | AATCTCCAGTGCCTA[G/T]AATGCCAAGCACATA | 5521 |
rs77962672 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671322 | AAACACGTCTCTGTC[C/T]TTAGGTTGTCCAGTG | 5521 |
rs77972848 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861871 | GTTTTTTTTTTTTTT[G/T]GGCTTGCTGCTTTCA | 5521 |
rs77982971 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815997 | ACTCCTCCAACCTAA[A/G]TCTGCTCCAGATTAA | 5521 |
rs78000402 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603292 | ATTTGAAAGACATAA[A/G]GAATGTTTACATTTT | 5521 |
rs78000487 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877184 | AAAAGGCAGAATGAG[A/C]TTCCACCTGCTGACT | 5521 |
rs78005138 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079082 | TCTTTTAGGTGACAT[A/G]AAATGGGATTGATAA | 5521 |
rs78009149 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818347 | TCTATGCTAAAAAAA[A/T]TTCACTGCAAAAAAA | 5521 |
rs78022777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872017 | CCCTCAGCTAAGTGT[C/T]GAAATTGGACCCCTA | 5521 |
rs78031234 | snp | A/T | 0.111576 | 0.20818 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603545 | GTGGAGTGCCGGCTT[A/T]AGGTAGCACACAGAG | 5521 |
rs78036046 | snp | A/G | 0.0325976 | 0.123435 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768660 | GATCTATAAGGTCCC[A/G]TACCATCTGACGCTG | 5521 |
rs78043176 | snp | A/G | 0.476574 | 0.105661 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014431 | gctataaagacacat[A/G]cacacgtatgtttat | 5521 |
rs78074625 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832805 | GTAACATGCTGTACA[A/G]GTTTATAGTCCAGGA | 5521 |
rs78082037 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635623 | GTGGCCCAGAAAGCC[C/T]GGTTCTGCCTTCACT | 5521 |
rs78093813 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629298 | CCTCGTTTCAGTGTA[A/T]GGTACCGTACAGTAA | 5521 |
rs78095545 | snp | A/C/T | 0.0146672 | 0.084371 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620693 | GGCCCACTCCACACA[A/C/T]CACAGGCTAGAGACT | 5521 |
rs78099204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661969 | GGGATTGGGAGAGGC[A/G]GTGGTTTAATTTTTG | 5521 |
rs78101316 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984805 | TTGTGGCTTTAATTT[A/G]CATTTTCCCAGTGAT | 5521 |
rs78109554 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056569 | AGGAACTGACCCTTC[A/G]TCAATCTGTGAACCC | 5521 |
rs78110218 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000755 | ATTGAGATAACACCC[A/G]TAGAGTACATAGTGT | 5521 |
rs78112063 | snp | A/G | 0.0225045 | 0.103662 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621781 | CTGATGCAGAGAGAA[A/G]AAACATTTTATAATC | 5521 |
rs78117711 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649451 | TATATTTTTTATTTT[G/T]ATTATTTTTTTGAGA | 5521 |
rs78118264 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049116 | TGTGTGTGTGTGTGT[G/T]TGTGTGTGAGATATT | 5521 |
rs78125026 | snp | A/C | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903287 | TTTGAGGTTCTCAAT[A/C]ATTTTTAAGGTTATA | 5521 |
rs78128262 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675435 | CCTGGACTGTGGGAT[A/G]GCAGGTTAGTTGCAA | 5521 |
rs78130387 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975480 | ATGGGTATGCAAATA[C/T]GTCTTTGAGATCTTG | 5521 |
rs78135009 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651068 | CTATTTTTTTTTTAA[A/C]CATGAAATCTATTTA | 5521 |
rs78140291 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069022 | CACCCACAGTAAAAA[A/T]TAAAATGAAAAAACA | 5521 |
rs78155988 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779366 | CTTGGATTTCCTATC[A/T]TAAGATCTGAACCCT | 5521 |
rs78166575 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052253 | AGTGAATGCTTTTCA[G/T]AATATTTTTCACATA | 5521 |
rs78210754 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656793 | GATCACCACCTTCAC[C/T]GTGCGGGTGAGGAAA | 5521 |
rs78210775 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979718 | TTACCTCATACATAC[A/G]TACCAATGATAAAGT | 5521 |
rs78212353 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040570 | TAATAAATGACTGTC[A/C]CAAATCCCCCGCCCT | 5521 |
rs78223704 | snp | A/G | 0.0048587 | 0.0490484 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055794 | CAGTCTCCTGAATCC[A/G]TAAGGATTCTCTCGG | 5521 |
rs78224402 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653902 | TCAGTCCCAGGCCTA[C/T]GTCAAGGCTTGTCTG | 5521 |
rs78228781 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973616 | TGTAATTCCTCACGT[A/G]TAACTCAACCCAAAT | 5521 |
rs78247062 | snp | A/C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657717 | CTTTTAATCAAGGCC[A/C/T]CATAGACGACCCCAT | 5521 |
rs78257660 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891760 | GCATCTAGTGGAATG[A/C]GAATAGCTTTGACAG | 5521 |
rs78261180 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966520 | TGACATGACCTAAGG[C/T]CCCTCCCTCAACACT | 5521 |
rs78272885 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072055 | CAGGGGAAGATGAGC[A/C]GTAAAAAAATTTCTG | 5521 |
rs78274660 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966210 | AGGCTCGTTAATGTT[A/G]TCATTGTTTATTATT | 5521 |
rs78275135 | snp | C/T | 0.081446 | 0.184634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980142 | ATGAAAAAAAGAAAT[C/T]CAGAACAGTATGTAG | 5521 |
rs78279630 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680564 | AATAATAAAAAAAAC[A/C]ACAGCGTTGCACACA | 5521 |
rs78280023 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625899 | GGAGAGAGACAGAGA[A/G]ATGTGATATGAGAAG | 5521 |
rs78281416 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798812 | GGAATTAACTTTCTC[C/T]AGGGTATACAGCTAA | 5521 |
rs78288581 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857417 | AGTCCATTATTGTTA[A/T]TTTTTTAGTATCTTA | 5521 |
rs78318624 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745957 | AGAGAGACTTGGTCT[A/C]AAAGAAAAAAAAAAA | 5521 |
rs78319083 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687043 | TGTGTGTGTGTGTGG[C/G]AGGGACAGTGGTAGC | 5521 |
rs78324360 | snp | A/G | 0.0711525 | 0.174681 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621131 | CCCTGGTGTGAGCTG[A/G]TCACTGCTTCACTGT | 5521 |
rs78324391 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863039 | CTGCTTTTGCTTTTT[G/T]TTTTTTCCACAGTGC | 5521 |
rs78329216 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033851 | CCTTTCTTGTCCACT[A/G]TGATAGCCTCTTATT | 5521 |
rs78332175 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838278 | TTCCCAAGGTTACAG[A/C]CTTAGAAGGAAGGAA | 5521 |
rs78332250 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785173 | ACACAATCAACCCTG[A/G]TGATATAAAAGGAGA | 5521 |
rs78336252 | snp | C/G | 0.0970103 | 0.197722 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955017 | CGATGGTCCTCCCAA[C/G]TAGGTATAATTTCCC | 5521 |
rs78363569 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870379 | TGCCCTTGCAAGAAG[A/G]AAAAAAAATGCCAGA | 5521 |
rs78428229 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784793 | AGAAAAGAAGGTTCT[A/C]TTATGTTAACTTTAC | 5521 |
rs78443050 | snp | C/T | 0.095934 | 0.196885 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933653 | ACCTATCGTGACAAA[C/T]GGAAGTTCTTTTTTT | 5521 |
rs78447365 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633432 | TGGAGAAAATCAATA[C/T]GAAATGTCAGGCGAG | 5521 |
rs78459986 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657752 | AGCTCATTATGATAC[A/G]TACAACATAATCAAC | 5521 |
rs78476464 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999885 | ATGTAAAGGCCACAG[A/G]GAAAGTCTTGAAACT | 5521 |
rs78559100 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888738 | CCACCACCACTCCCT[A/G]TAGACATGGAAGGAA | 5521 |
rs78568592 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606669 | GCCTAGTGTTTTTCC[A/G]TTTGAGGCAGATCTT | 5521 |
rs78592301 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803580 | ATTCTAGCTAAGTCA[G/T]GCAGCTTTATTTAAG | 5521 |
rs78599606 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887772 | CCAAAAGGGCACTTT[A/C]ATATCTGGGCATCTG | 5521 |
rs78610694 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745122 | GTGTCAGTTGTCTTG[A/G]CTCATTTTCCCCCAA | 5521 |
rs78612376 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852760 | CCTAAGTTCACAATA[C/T]GATGGCTGATTAGAG | 5521 |
rs78613342 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949544 | GGAAGTAGAGAAAAG[C/G]CAAGCCTCTTATGCT | 5521 |
rs78614284 | in-del | -/TT/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828255 | AAATATTACTTTTAC[-/TT/TTT]TTTTTTTAAAAAAAA | 5521 |
rs78617387 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077787 | GCACTTTCCAAACAA[A/G]ATAGGGATTGTCATT | 5521 |
rs78622389 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822564 | TTTGCTTTTTAGGTT[A/G]TCCTGTCAAGAATAC | 5521 |
rs78652028 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030865 | ACATACAACACTTTT[C/T]ATTATGGTTCACTCA | 5521 |
rs78658159 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053226 | CATTAAAAAAAAAAA[A/C]CACACGCGCACACAA | 5521 |
rs78665906 | snp | A/T | 0.0360663 | 0.129354 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940209 | TGTTGATCTTTCCAC[A/T]CCACTTTGTCTTAAT | 5521 |
rs78672626 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726234 | CAAGCACTTACTGGG[A/C]GTCAAACAAGCAGGA | 5521 |
rs78676518 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631522 | GCCTTTCAAGGTATC[A/G]CTTTTACTATTCCCA | 5521 |
rs78682355 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795794 | ACAAACTGTTTTGTC[A/G]ATTACATCTCAAAGC | 5521 |
rs78685385 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984777 | AATTCTGACAGGTGT[A/G]AGAGGATATTTCTTG | 5521 |
rs78688142 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049669 | GAGGGAAACAGAGAG[A/G]AAGAGTGGGTTTTGA | 5521 |
rs78690977 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650293 | AATTCGTGACATATA[A/G]ATGCCTCTGTATGAA | 5521 |
rs78703444 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606894 | ATGAGGGTCCGCTCA[C/T]GATGAAAAAGGAACG | 5521 |
rs78704395 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990250 | AAATTCATGTGGAAG[G/T]GCAAAAGACCCTGAA | 5521 |
rs78723580 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941067 | AATGAGTTTCCTGGA[A/G]ACTTGTCTTCTTTGT | 5521 |
rs78736990 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958226 | CTTTTATTTTCCCTT[C/G]AGGATGCTCAGCTGC | 5521 |
rs78740685 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027636 | CGAGACTCGGTCTCA[A/C]AAAAAAAAAAAAAAA | 5521 |
rs78744131 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677205 | ACTGGCAAGATAATT[A/G]GACAGAGTTTTCGCT | 5521 |
rs78745287 | snp | A/T | 0.0325976 | 0.123435 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913490 | AACATATAGTTCCAG[A/T]AATGACTGAAATTCT | 5521 |
rs78749196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805442 | CTCTTTGTTGTCTAA[C/T]TGCAACAAAAATCAA | 5521 |
rs78762191 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804819 | CTGAGGAGAAGCATA[C/T]GTTTAATGCTTCACA | 5521 |
rs78763875 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840685 | TTTGACTCCAATTTG[G/T]TTTTATACAAAACAA | 5521 |
rs78778049 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686290 | AGAGGAGGCAGACAG[C/T]GAAGAAAATGCTAGA | 5521 |
rs78802933 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037461 | GTATGTAATTATAAA[C/T]ATATATATGTATCAA | 5521 |
rs78833524 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626708 | AGCCATCTATAACCC[C/T]ATGGCCAATCTTTCC | 5521 |
rs78833738 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838570 | AGTGAGCCTCCATCT[A/C]AAAAAAAAAAAAAAG | 5521 |
rs78837128 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080106 | TATAGCAAGATTTTA[A/T]ATAAACTGCCTCTTT | 5521 |
rs78838754 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060618 | TGGTGACAAAGTAAG[C/T]GAGAGTCTGTCTTAA | 5521 |
rs78839383 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033508 | TTTGTGGAATGAACC[C/T]GAGAAGATACTCATA | 5521 |
rs78840917 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011079 | TCTGGATGCCTTTCC[A/G]ACTACTGCCCCTTCT | 5521 |
rs78841787 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865967 | TAATACTGTTTGGAC[C/T]TCTATTAGGTTCCCG | 5521 |
rs78864746 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995972 | GGCAGAGTTCAAATT[A/T]CAACACTCTAGTCAT | 5521 |
rs78889991 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934988 | ATCAGTTACCATTGA[C/T]TAATTTATGCATTTA | 5521 |
rs78901590 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804512 | ATTGACTATATTTTC[A/G]ATAACAACATAAACA | 5521 |
rs78904967 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961571 | TGAACACCTTTCCAT[A/G]TAACTATCAGGTGTG | 5521 |
rs78905242 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592338 | ATGCTTTCAAACACT[A/G]TTATTGGTGCCACCT | 5521 |
rs78911764 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712922 | GAACACACCAACTAC[A/G]TGTAAAGTACTATTC | 5521 |
rs78913713 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146765979 | TTTTTAGACTCTCCA[C/T]TTATTATCATCTGGT | 5521 |
rs78917117 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925362 | AGTCTCTGTTTATCC[A/G]AAAATGTCCTTATTT | 5521 |
rs78920244 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015527 | AGCCATCTCCTTCAT[A/G]GAGCCTTCTCTGATT | 5521 |
rs78920915 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963261 | GCTGTCTTCATGGAG[C/G]TTTTGTGTAGTGAAA | 5521 |
rs78932356 | snp | C/G | 0.04875 | 0.148319 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920113 | CAGGCCGTACATGAA[C/G]GTTATAGTAATTATT | 5521 |
rs78942869 | snp | C/G | 0.113685 | 0.209567 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712728 | CCACTCTGTGCATCC[C/G]TCCCAGAGCTGCACA | 5521 |
rs78958230 | snp | C/T | 0.101301 | 0.200969 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638676 | TATCCTCTATAAACA[C/T]GTAAAAGACATCCAC | 5521 |
rs78971461 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032486 | CTCTGCACCATATTT[A/G]TAGTATTTTAGCTCT | 5521 |
rs78979234 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626462 | TGAAAAAATGGAAGA[C/T]AATTTTTGGTTTTTG | 5521 |
rs79004358 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885027 | ACTGGAAACAACCCA[A/G]ATGCCCAACAAAATA | 5521 |
rs79005587 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872792 | AGTGTGTGGTTATTT[A/G]TGCTTACCAAGGCCC | 5521 |
rs79014095 | snp | C/T | 0.182706 | 0.240773 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080685 | TCCCTCTGCACTTCA[C/T]GTATTGCCAATGGTC | 5521 |
rs79014757 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620036 | ACCTGCCGGGCACCA[A/T]CTAGGGTAAGAATTA | 5521 |
rs79015313 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595829 | TTCTTCATGTTCCTA[A/G]TATGACTTTTCTATG | 5521 |
rs79019519 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075142 | GTTATCTGATATCGA[G/T]TGGGAAATTTTTACC | 5521 |
rs79020343 | snp | A/G | 0.237014 | 0.249662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673346 | TCTTAATTTGCAAAC[A/G]TTAACTGGGTTAATA | 5521 |
rs79021817 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692203 | TGAACAAATCTCATC[C/T]ACCTGCATAGTACAT | 5521 |
rs79041550 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631470 | CCACTTGCTCCATCT[C/T]TGTGTCCCCAGGTCT | 5521 |
rs79059404 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627910 | ATTGGAACTCGGGCT[A/G]TTTCTCCAATGACTA | 5521 |
rs79064828 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711086 | TATAAGTTATCACCA[C/G]TAATCATTAGCATTT | 5521 |
rs79064907 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778143 | GGCAATTTGGGTTCC[A/G]GCATTCCTGATAAAA | 5521 |
rs79066938 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861593 | CTCCATGAATTGTTT[C/T]TCACCACAATGGCAG | 5521 |
rs79092730 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654868 | TCCTCCACAGGACCA[C/G]AATGCCCTTTTGCCA | 5521 |
rs79103560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052313 | CTTGGTATTTGTCAT[C/T]TTTCATTCAACAAAA | 5521 |
rs79106879 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607419 | AAATAATGAAACCAA[C/G]TTGCTTAACCCTTGC | 5521 |
rs79114407 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902955 | CCATTTTCATAATAC[A/G]AAGATGTTATTTGCT | 5521 |
rs79130125 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742097 | AAAGGAAAATGTTAT[A/G]TATGTGTCAGAAAAA | 5521 |
rs79133865 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883333 | AAAATGACCCTTCTT[C/T]CTCCTGCGGTACTTC | 5521 |
rs79142342 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999306 | GGAAGGTGGTAAAAA[G/T]GATGTCTAGCTTATG | 5521 |
rs79150247 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639054 | CCTTATCCTCATTTT[A/T]TCAGGGGTGGAAACG | 5521 |
rs79163311 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832959 | CCTATCATTAACTGA[C/T]GCATGACTGTGTGTA | 5521 |
rs79168900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724542 | ATATATAGTTGCAGT[A/G]AGAAAAATCTATAAA | 5521 |
rs79220680 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606385 | TGGTGACTAACAGTA[C/T]AGGTGGTTCCAAACA | 5521 |
rs79220749 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758465 | AAATTAATAAAATAC[A/T]AATACGGCACTATCA | 5521 |
rs79238917 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654290 | GGGAGGTGGAGTATC[C/T]AGTCCAATGTCACAC | 5521 |
rs79239834 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798708 | GCTCTAGGCACATAG[C/T]GAGATGCTTTGCTTG | 5521 |
rs79259064 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707846 | TCTATAGACAAAAGT[G/T]TATCAGAGAGAATCC | 5521 |
rs79290112 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978777 | CTTCAAACTACACTA[C/T]AAGGCTACAGTAACC | 5521 |
rs79305368 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739436 | AGGGCAAAGGATGGG[A/G]AGGAAAGAATGCCAG | 5521 |
rs79306093 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726499 | TGAACAACCCATTAG[A/G]CACACTTCTAAGCAC | 5521 |
rs79318326 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847062 | TTACACTACTGTTCA[A/G]ATCCTTTAATTCTAC | 5521 |
rs79321864 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952344 | AGACAACAGCATCCT[G/T]CTGGGGCACCTCTTT | 5521 |
rs79322886 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658290 | GGCACTAGACGGTAA[A/C]TCTCTCAGAGGGGCT | 5521 |
rs79323749 | snp | A/G | 0.123105 | 0.215401 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994317 | AAGTGGCTGAGTCAG[A/G]AGGGGACTCAGTCAT | 5521 |
rs79331363 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981176 | ATAGCAGGCACTCTA[A/C]AAATATTTGCTGAAG | 5521 |
rs79336445 | snp | A/C | 0.11228 | 0.208646 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725043 | ATATATACTTCTATT[A/C]ATGCGATCAATAATT | 5521 |
rs79343193 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877254 | ACAAGCTGGGAGAGA[C/G]GGAGAGACGACAATT | 5521 |
rs79351763 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995974 | CAGAGTTCAAATTTC[A/T]ACACTCTAGTCATGA | 5521 |
rs79355475 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010674 | ACAGATGAAGCTTCA[C/G]TTTGCTTGCCCGCCG | 5521 |
rs79356680 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053227 | ATTAAAAAAAAAAAA[A/C]ACACGCGCACACAAA | 5521 |
rs79358570 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074191 | GCACAATAAGGTTGG[A/G]AAATTATTCAGTATC | 5521 |
rs79362000 | snp | A/G/T | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893665 | CTAAAAATACAAAAT[A/G/T]AGAACACATGGACAC | 5521 |
rs79382956 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924558 | AAATGGGATACAGTA[A/G]CCTCTTGCTTTTTAT | 5521 |
rs79393475 | snp | A/C/G | 0.00875189 | 0.0656212 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799552 | AGCCTGAGACAACAC[A/C/G]TGTCCACTCATGAGT | 5521 |
rs79393855 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015304 | TATGACTGTAAAAGG[A/C]AGTTCACCTTGCTTA | 5521 |
rs79395952 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888718 | AAATTTCACCTCCCC[C/T]CCCACCACCACCACT | 5521 |
rs79404963 | snp | A/G | 0.105569 | 0.204058 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608227 | ACAGTGGGCCCCTAG[A/G]ACTGGTAGCACCATG | 5521 |
rs79445591 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702997 | AGACACCTCAAGTGA[A/G]TTATTTGACCACTTT | 5521 |
rs79450659 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974706 | ATTTTTTTTTTTTTT[G/T]TGAGATGGAGTCTGG | 5521 |
rs79450821 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705820 | GCCAAGATGACCTTG[C/T]TGAAAGATGTTAATA | 5521 |
rs79458952 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949310 | CTCAATGGGAAAAAA[A/T]TCTAATAATTTGATT | 5521 |
rs79478174 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633498 | GCTGGGGCTCGTAGC[C/T]GCAGCAGCTGAACAA | 5521 |
rs79481597 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644091 | TAGCAGAGTAAGAGG[C/T]GAATTGTTTATTGCT | 5521 |
rs79484443 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690256 | GTTCATAACTGAGCT[A/C]ATCATCCAGTCCTAA | 5521 |
rs79499595 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677419 | AATGAAGTACATGCC[A/G]TCACCATTTTTTTTT | 5521 |
rs79510835 | snp | A/C/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646664 | GCAAAGGACACCCAA[A/C/T]TGCAGAACCAAAGGA | 5521 |
rs79526861 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958349 | CTTTCCATTCCATTT[C/T]TGAAGGAAATATCAC | 5521 |
rs79531963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956853 | TCCTTACATCTTTAC[A/T]TGGTGGAAAGAGCAA | 5521 |
rs79539895 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694870 | GGCATACTTAGTTTA[C/T]AGTATGCATTTGCCT | 5521 |
rs79540814 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017209 | GGGCAATAGAATCAG[C/T]AGGATTTGGTGATTG | 5521 |
rs79549380 | snp | A/G | 0.0178098 | 0.0926698 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082224 | TTGAATTCCTATACG[A/G]AAACCTTCATCTGCT | 5521 |
rs79562136 | snp | A/C | 0.0327778 | 0.123752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789911 | TCAGGCAGGCAGGGG[A/C]CAGATCAGGGAGACA | 5521 |
rs79563653 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949415 | AGTGCTCAATGTCAT[C/T]GATCATCTGAGAAAT | 5521 |
rs79564190 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913250 | ATTATTGCCTCTTCA[A/G]GATGGTAGGAGAAGG | 5521 |
rs79564410 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641068 | TGGGATGATGAAGTT[A/G]AGAGGAAGATATGGC | 5521 |
rs79574804 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717333 | CAAATACTGATTCCA[A/C]CAACCTAAGTTATTG | 5521 |
rs79594328 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065658 | AGCGAGGTTGAGGGA[C/T]TGGAGATACTGACCT | 5521 |
rs79595513 | snp | A/G | 0.237882 | 0.249706 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673972 | CATGTTGAGGTCAGT[A/G]TGTCTTAGGCAAATA | 5521 |
rs79657188 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054494 | AACTGTAAAAAAAAA[G/T]TCCATGAGATATCAA | 5521 |
rs79672291 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904223 | AAGAAGGAGAAAAAA[A/T]TTTTTGAAGATCAAA | 5521 |
rs79673749 | snp | C/T | 0.084728 | 0.187577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680569 | TAAAAAAAACCACAG[C/T]GTTGCACACACTTAA | 5521 |
rs79683351 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016335 | GTAAGACTCTGTCTC[A/C]AAAAAAAAAAGATGA | 5521 |
rs79695843 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727793 | TCTCTAAAACTTCTT[C/T]TTCTTGTGTAATTGA | 5521 |
rs79700388 | in-del | -/TCA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686624 | AAAATTGTATTCATC[-/TCA]ACATCACCTTCATTT | 5521 |
rs79701672 | snp | G/T | 0.031825 | 0.122064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760236 | TGTACCCTCTTAATA[G/T]TCCTGGCAACCCTAT | 5521 |
rs79710605 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608898 | CAACTGTTACAAAAA[A/G]ATAGAGGAGGGAATA | 5521 |
rs79733318 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687058 | CAGGGACAGTGGTAG[C/G]GGGGAGTGGTGGGGG | 5521 |
rs79741093 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815132 | CATCCCTGAAGGATG[C/T]GCATGCTGGCACTGC | 5521 |
rs79746207 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048960 | GTGGGAAAGGACAGG[A/C]AAAAAACAAGTAAAT | 5521 |
rs79773558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607629 | TCTTTTACAACATGT[C/T]TTTTAACAACTAATC | 5521 |
rs79773641 | snp | C/T | 0.133777 | 0.221342 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064749 | GTTGCCATTTGGTCT[C/T]ACCTAGCTCTTTAGG | 5521 |
rs79789134 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668865 | CCATAGAATGGAAGG[A/C]AGCAGGGCACGGGTG | 5521 |
rs79791367 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888735 | CCACCACCACCACTC[C/T]CTATAGACATGGAAG | 5521 |
rs79795820 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863079 | TGTAGGTCCTGGTGG[A/G]TGCTTACCAAGTTTC | 5521 |
rs79796434 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681245 | TTGCATAACCTAGTA[C/G]CAAAAAGGGATCTAG | 5521 |
rs79800174 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936245 | TTCAAGAAAGCAAAG[A/T]TTTCCTGCTGTAAGC | 5521 |
rs79800841 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708335 | GCACTCACACCTGGG[C/T]GACAGAGCCAGACTT | 5521 |
rs79801335 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895920 | ATATGTCCTGTCACA[C/G]ACCAGTCCGTGATTC | 5521 |
rs79811240 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064176 | TCATCAGTTCCTCTA[C/T]ATCTGGATTACATCT | 5521 |
rs79819475 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906666 | TGATTATGCATCATC[A/G]TATTTATGGGGCACA | 5521 |
rs79821472 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770330 | AGTGAGATTCCGTCT[A/C]AAAAAAAAAAAAAAA | 5521 |
rs79821623 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872723 | CTGGACTCTTCTTAT[C/T]CTACCACATTGCTGA | 5521 |
rs79827249 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609339 | CTCAACATAGTACTG[A/G]AAGTCCTAGATAGAG | 5521 |
rs79827935 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651069 | TATTTTTTTTTTAAA[C/T]ATGAAATCTATTTAA | 5521 |
rs79829031 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590396 | TTTTGTTTTTTTTTT[G/T]TGTTTTTTTTTTTTT | 5521 |
rs79834748 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788123 | TGTGTGAGCATTTGC[A/G]CAAGTTGCCTCCAGT | 5521 |
rs79844708 | snp | C/T | 0.0799831 | 0.183287 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770069 | TGTAGTGGCTCATGC[C/T]TGTAATCCTAGCATT | 5521 |
rs79848851 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841291 | CTCATCCAAAAGGCA[A/G]CATTAACTACTCTTG | 5521 |
rs79855607 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845629 | GAACAGACACTGTGC[A/G]TGGTCAGCTCATGAT | 5521 |
rs79863274 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795991 | CCTGCATATAGACTA[C/T]CCCTACGTTTTGTCA | 5521 |
rs79869066 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657740 | GACCCCATCCCCAGC[C/T]CATTATGATACGTAC | 5521 |
rs79930577 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792312 | TGTTAAATAGTTCAA[A/G]AGCCCAGCCAAAAAC | 5521 |
rs79930981 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027738 | TCTGTATCTTCACTG[C/T]GGTGATGATCAATGG | 5521 |
rs79940695 | snp | A/G | 0.199254 | 0.244796 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685478 | TAATCAGTTCTCTAG[A/G]AGACAAATCAAGTAA | 5521 |
rs79956066 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675561 | AGGATGAAACATATA[A/G]CAAGTGCAATATTAA | 5521 |
rs79969648 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071493 | TCTCCATCTTTCACA[A/G]CTTCCTCCTTTGCCT | 5521 |
rs79971827 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687307 | GAGGCTGCATCGGAT[C/T]GAAGGGCTCAGGTCC | 5521 |
rs79986461 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595127 | CACTTCCAAACAGTT[C/G]CAGGCCTTGTCAGGG | 5521 |
rs79988490 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621213 | CAGGAAAACACTGCT[C/T]CTAATCCACTGATCC | 5521 |
rs80003520 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908483 | GAACATACATATGTA[C/T]ACAGCTGTTTGGGCC | 5521 |
rs80005726 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593228 | TTTTAGCTGTAGGAC[A/C]TTAGGATGGGTTGAT | 5521 |
rs80015525 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074035 | AGTGAGGCTCTGTCT[A/C]AAAAAAAAAAAAAAA | 5521 |
rs80028791 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808750 | CTCTGAAATAAAACA[G/T]AATTGACTTGCCAAG | 5521 |
rs80032804 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877211 | GACTTTCCCTTCCTG[C/T]CCGCACAGCACTAGT | 5521 |
rs80040773 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634778 | TACACACACACACAC[A/C]CACACCCCCTACTGG | 5521 |
rs80053355 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912512 | CAACTTTTCTTTTTT[C/T]TTTTTTTTTTTTTGT | 5521 |
rs80054962 | snp | A/G | 0.079617 | 0.182947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639298 | AAGTTTTAGGGTCCC[A/G]TGGAAAATATCCTTA | 5521 |
rs80066437 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825532 | TGCTTGCATTTCTAT[C/T]TGTATCATAAGTGTT | 5521 |
rs80075130 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037168 | TTCAGGGAAAAAAAA[A/T]TATTTTTGCCTAAGA | 5521 |
rs80075321 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925326 | TCTTTTAAAACAGGG[A/C]TGCTAGCAATACATT | 5521 |
rs80076459 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650055 | ACTTTTCTATATGCA[C/T]AATATACTTCAATGA | 5521 |
rs80080378 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741592 | TATAATACGAAGGGC[A/G]ACCGCCTCTCGGGAC | 5521 |
rs80085782 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925628 | TGTGGATCTATTTGT[A/G]TTTATCCTGCTTGGG | 5521 |
rs80090785 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035377 | CCAATCACCTCCCCC[A/G]AGTTCCCTTCTTCAA | 5521 |
rs80112816 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886857 | AGTATTTTTAATGCC[A/G]TGAAATACTTTATAG | 5521 |
rs80113420 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823704 | ATATGTTGTTCTTCT[C/T]AAGCAGAAGTATAAA | 5521 |
rs80125615 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776558 | ACTGTTGCAAGAAAA[C/T]ATAATGGCAAATGTG | 5521 |
rs80129359 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780140 | TGGACCTATTATGTG[A/G]CCAACACTTTGTAGA | 5521 |
rs80136409 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077933 | GGCATATGTGTAAAA[C/T]GCACATTCCAGGCCC | 5521 |
rs80145411 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723740 | CTGATCTTCTAACAG[G/T]TCCTGAAACCCTTCT | 5521 |
rs80155239 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687482 | GGTATATGGCAAATG[A/G]TCAATAAGTGCTAGA | 5521 |
rs80159546 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693626 | AAATAATTTAGTATG[A/C]GTATATCCCATATAG | 5521 |
rs80172036 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621605 | ACAGAGAATTAACCA[C/G]AGTGGAGCCATCTCT | 5521 |
rs80172932 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595870 | TTTGTGCATGGGATT[C/T]TGGACGCCAGACTGA | 5521 |
rs80192862 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852132 | ACAGAGAAAGGGGAC[C/G]AATAACAGCATCCTC | 5521 |
rs80193182 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671203 | CTTTGGGAAACACAA[C/T]GATATACACCAAGGT | 5521 |
rs80195078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784267 | AAAATTTAGTCACAA[C/T]TAAAAGTGTGAGAAG | 5521 |
rs80204737 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939009 | TGGTCTCGAACTCCT[A/T]AGCTCAGGCAATCAG | 5521 |
rs80215914 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757492 | GAGTTTAAAGGAAAA[C/T]GGGTGGAAGGCGAGA | 5521 |
rs80237796 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606895 | TGAGGGTCCGCTCAC[A/G]ATGAAAAAGGAACGG | 5521 |
rs80253669 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146765989 | CTCCATTTATTATCA[G/T]CTGGTGATTAAAGAA | 5521 |
rs80275561 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598758 | TCTGGCTACCTTCAT[G/T]GCTAATACACTCATC | 5521 |
rs80283457 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008834 | TTGTTGATTGTCAAA[C/T]TTTAATCACAGCAAA | 5521 |
rs80290347 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023638 | AAAATGGGACAATTC[A/G]TACTAACTGATAGGT | 5521 |
rs80290788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811315 | ATGGCTCCTATCTCT[A/G]TTAGTCTATAGTAAG | 5521 |
rs80307097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949163 | GACATGAGTGGTACT[A/G]TTAAGCTTCAAGAAT | 5521 |
rs80310654 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925270 | TGGATTTGTGCTATC[A/T]TAGAGTACCATTTCC | 5521 |
rs80313965 | snp | C/T | 0.309894 | 0.242719 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687436 | ACCCTTTGAGGTAGC[C/T]AGTGCAGATAGAGAG | 5521 |
rs80320674 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745961 | AGACTTGGTCTCAAA[A/G]AAAAAAAAAAAAAGA | 5521 |
rs80321852 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060263 | ATTATTGAGCATATT[C/T]ATTGAATACTTACTT | 5521 |
rs80326843 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592511 | ATAAATCACTTTGAG[A/G]GAATGTGATAAATGA | 5521 |
rs80355963 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977366 | CCTGTGTAACAGTCT[A/C]TTTTAATATTATTAT | 5521 |
rs111230058 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676085 | ATGCCCTGACATGTA[C/T]TGAAACAATGGCAGC | 5521 |
rs111233290 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956908 | TGAGGGCATTAATCC[C/T]ATTTATTAGGATTCT | 5521 |
rs111249931 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704517 | CATTTTTCCTCTGTT[G/T]TATATAGATGTGGAT | 5521 |
rs111254614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030674 | CCAGAAATTGCAACA[C/T]ACATCTATTAATTAT | 5521 |
rs111255071 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711992 | AGGACAAATTGAACA[C/T]TAAATACAATGCATA | 5521 |
rs111257622 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055170 | ACTGCTCTGTAACCC[A/G]AGTACAGACTCCAAG | 5521 |
rs111261586 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637022 | CGTCTCTGAATGGCC[G/T]AACCCATAATTATCT | 5521 |
rs111263360 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855700 | CAAACTCCACCTCTA[A/G]AGAGAATCTCTGATG | 5521 |
rs111274958 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897166 | AGGTAAGTGGAGGAA[A/T]GATGACAGATTGAGG | 5521 |
rs111275795 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843174 | CCTGGGCAATGAGGG[C/T]GAAACTCTGCCTCAA | 5521 |
rs111278506 | in-del | -/AC | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634764 | TAAATCTCTTAACTT[-/AC]ACACACACACACACA | 5521 |
rs111284010 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652746 | ATGAGGTGACAGGCT[A/T]GGTAGGAGGCAACAC | 5521 |
rs111284293 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080414 | GCTATTCTAGTTCCT[C/T]CCAATTGCCTATCAT | 5521 |
rs111289099 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602380 | CAGATAAATTAACAG[A/G]TTCTTTGCCTTCTGG | 5521 |
rs111289348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728744 | ATCTGATGGGTTTAT[C/T]AGGGGTTTCCACTTT | 5521 |
rs111340013 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948398 | GGGAGGATGAAATGA[C/G]TTAATGCATGTGAAG | 5521 |
rs111346525 | snp | C/T | 0.000527426 | 0.0162307 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600345 | CCAGACTTTGACGGT[C/T]AAGTAGTCCCTGGTC | 5521 |
rs111349413 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634785 | ACACACACACACACC[C/T]CCTACTGGTTCTGTT | 5521 |
rs111354087 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943563 | TTCTTTAAATTGCAA[C/T]CTTGGCACATTTGGG | 5521 |
rs111355832 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593757 | AATCCTGGAGGGAGT[A/G]TGGTGGGAGAGGAGT | 5521 |
rs111365841 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762325 | CTCACTTCAGCATTC[G/T]CTGAAGGCATCAGTT | 5521 |
rs111373602 | in-del | -/GAGA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764801 | GAACATCTCTATCCC[-/GAGA]GAGAGAGAGAGAGAG | 5521 |
rs111379586 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053812 | CAGTTCATCTCAACA[A/T]CCTTGTTATAGATAA | 5521 |
rs111380647 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883727 | TCTAGCAAGTTTGCA[A/G]TTCCTGTTTGTGCAT | 5521 |
rs111404340 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076273 | TAAGTAAAAACATCA[A/G]TTTACAAAATAGTAT | 5521 |
rs111413844 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004406 | GGGTACATTTAACCA[C/T]TGAGGACCAGGAAAT | 5521 |
rs111417333 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762776 | GACAAGTAATTATAA[A/G/T]GCAGTGTAATTGTTG | 5521 |
rs111437635 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599846 | ATGTTCCCCTTCCTG[C/T]GTCCATGTGAACACA | 5521 |
rs111462050 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739592 | ATTAGAGAAGTAAAC[C/T]TGAGGTTCATGAGGA | 5521 |
rs111478764 | snp | A/G | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727102 | AAACTACCCTTCAGG[A/G]AATTCAAAATTGCTC | 5521 |
rs111490947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784695 | ATTTCTTTTTGTGTG[C/G]CTCTCAGCTCTTCAG | 5521 |
rs111496908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906773 | CTGGCTCACCTTATA[C/T]GTCTATTGGGCAGTA | 5521 |
rs111500956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927124 | AGATTCCCAGTGTTC[C/T]TGAGTGATGTCCCAT | 5521 |
rs111531446 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616130 | CAAGAACATACACTG[C/G]GGGAAAAGACAGTCT | 5521 |
rs111541983 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717996 | CTTTTTCTTTAATGC[A/T]TCTACCATAATTCAT | 5521 |
rs111575394 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877138 | TTTTGGCACTGGGGG[A/G]AAAAAATGCCTCTAC | 5521 |
rs111580764 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072803 | ATCACCCAGGGAACC[C/T]GAGCAAATAGCACAA | 5521 |
rs111583514 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869219 | TACACAGAAAACAAA[C/T]AGAAGACCACAGATT | 5521 |
rs111595117 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740033 | TTATCATTTTCATCA[A/G]ATTCTCAAAGGAACC | 5521 |
rs111647074 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677047 | TCCTGAACTCCTATC[C/T]TTGTTGTCTGCTTTG | 5521 |
rs111660230 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706525 | CACGCAGCTGCCGCG[C/T]CATGTCCTACTTGGT | 5521 |
rs111660313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960629 | AATTAGAATGGAAAA[C/T]CATTAGACCTGCATG | 5521 |
rs111665994 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066661 | TTTTCAATAAGTGTC[A/C]GGCACCGTATTAGAC | 5521 |
rs111682271 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737952 | CTCAAAAAACAAAAC[-/A]AAACAAAAAAAACGT | 5521 |
rs111704646 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993055 | TCAAGTGATTCTTGT[C/G]CCTCAGTCTCCTGAG | 5521 |
rs111713382 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723824 | TTTCTCTTCCTCCCA[C/T]CTTACAAAAGCTCCT | 5521 |
rs111718161 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690227 | GTGCCTGCTTTACTG[C/T]TCACATTGAACATGT | 5521 |
rs111726338 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763785 | TGGAATGCACTGGTG[C/T]TATCATGGCTCACTG | 5521 |
rs111727733 | in-del | -/C | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683120 | GATGACTTAGATGTT[-/C]CCAGAGTCTGATGAT | 5521 |
rs111731757 | in-del | -/T | 0.369346 | 0.219673 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876419 | ACATGAAGGCAGCTC[-/T]CTTTCTTTGTGGTTA | 5521 |
rs111733568 | in-del | -/T | 0.0685596 | 0.171987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655434 | CGTGACCATCCCACC[-/T]CAAATCGCACAGCCT | 5521 |
rs111738658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880150 | ATCCCTGGGAGAAAA[A/G]AGCAGAAATGTTCCT | 5521 |
rs111738781 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665236 | GGATCTTCTTCCAAC[A/G]TAAGGCTCTCTTGTC | 5521 |
rs111742196 | in-del | -/A | 0.398174 | 0.201356 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752769 | AACAAAAATGAGCAG[-/A]AAAAAAGCATTGCCT | 5521 |
rs111752688 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846177 | TTGAGCCCAGGAGTT[C/G]GTGACCAGCCTGGGC | 5521 |
rs111753918 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636682 | GGAACCAGACTCTGG[A/G]TATAATATAAGTACT | 5521 |
rs111755988 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803643 | TCAAAGCCCTATGAC[A/G]TGTGCAGCTCCTAAA | 5521 |
rs111765994 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620741 | CTCACGTCTCTCCCC[C/T]TGAGATAGCATGCTC | 5521 |
rs111776962 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783534 | CTTTTTCCATTTTCC[A/G]AAGTCCATACAACTT | 5521 |
rs111778981 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013470 | GGAGGCATCACACTA[C/T]CTGACTTCAAACTAT | 5521 |
rs111779592 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881708 | TGAGCCACCATGCCT[A/G]GCCTCACTAGATCTT | 5521 |
rs111779691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670269 | TCCTAAACTGGCTTT[A/T]AAAAAAATCAGAATC | 5521 |
rs111786719 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629522 | AATGGTCTCTCTGCT[C/T]TCCAGGCCTGGCACC | 5521 |
rs111805330 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958981 | GGGATTCAAACAATT[C/T]AAAAAAGCTGTTGAG | 5521 |
rs111807717 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932998 | AAACTGTTTCTTTAC[C/T]TGTACCAGCACTAAG | 5521 |
rs111808212 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796009 | CTACGTTTTGTCACT[A/G]TTGAACTCAGCTGCC | 5521 |
rs111814042 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771934 | GATCAGAATGTGTGT[A/C]CCTTCAGAGATACAA | 5521 |
rs111816220 | in-del | -/ATCA | 0.106633 | 0.204807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725049 | ACTTCTATTAATGCG[-/ATCA]ATAATTCATAGAAAT | 5521 |
rs111816688 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669144 | CCTGACTTCCACCTA[-/T]TTTTACATTCTATTT | 5521 |
rs111822303 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073016 | CACACTGGATTGTCA[C/T]TAAAAACCATGTGGT | 5521 |
rs111823208 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077507 | AATAATTTTTATTGA[C/T]TTTGAGCGTATAGAA | 5521 |
rs111826674 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624853 | GGTACTGTACACAGC[A/C]CAGCTGGTCATCTTT | 5521 |
rs111829692 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619823 | CTTCAGGGCTCACTG[A/T]CTTTTTCTAGAAAAA | 5521 |
rs111842833 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687686 | GGGGATATAGTTTTC[A/G]TAGACATGCTTCTCA | 5521 |
rs111843874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891925 | GCATTAAACCAAGCA[C/T]AGGACCCTTCTAAGA | 5521 |
rs111852408 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935885 | TGATTCCCAGTTCTC[A/T]TCTTTCCCAGCAACT | 5521 |
rs111861609 | snp | A/G | 0.359152 | 0.224913 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016554 | TCTGAGAAAACATAG[A/G]GGACACAGTCACATA | 5521 |
rs111870052 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704357 | TTTAGAGATAATAAC[A/G]TCATTTGAAATCATG | 5521 |
rs111891679 | in-del | -/T | 0.107643 | 0.20551 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019596 | GTTTTGTTTTTTTTT[-/T]AAAAAGTCTATCTAT | 5521 |
rs111894717 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881061 | CTGTGGAGCTGGGGG[A/G]CGGGGTGGGGGAGAG | 5521 |
rs111900832 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600604 | AGTTGCTAATAGAGA[A/G]CTGTCATCTCTCTGG | 5521 |
rs111901083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078515 | TGTATTGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 5521 |
rs111902332 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013424 | AAGAGCCCGCATCGC[C/T]AAGTCAATCCTAAGC | 5521 |
rs111903173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912096 | ACAAAAAAGTTAGCC[A/G]GGCATGGCGGCATGT | 5521 |
rs111907600 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688096 | CACTGGGATCAAAAA[A/G]AAAAGGAAGCTGGAC | 5521 |
rs111913153 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941829 | TCACAAACTAGGTGT[C/T]TTAAATGACAGGCAT | 5521 |
rs111928450 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627489 | TATGTTCTGTGTAAT[A/G]GCAGAATTAATTCTA | 5521 |
rs111933258 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788328 | TTTTTCTTTAGCACA[A/C]CCTGGTTTAAAGAAA | 5521 |
rs111938339 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008378 | GTTAATTTATTCATA[A/G]AATATTTTAATTCAT | 5521 |
rs111941981 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624417 | TTCACCCTCTACATC[-/T]TTTTTTTTAAAAAAA | 5521 |
rs111954172 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063786 | TTGGACAGATGAGAA[C/T]GTTAGAGGATTTGAA | 5521 |
rs111956372 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970086 | CCATCCACCCTCTTT[A/G]CATCCTCCCACTGTT | 5521 |
rs111959016 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900120 | ATTTATTGAGCCATG[C/T]CCTTCCTTTGCTAGA | 5521 |
rs111960263 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691486 | GCTCTTAAATCTATA[C/G]CTTATACCTTAATTC | 5521 |
rs111969598 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039545 | AGATCTGCAACTGGG[A/G]CCTGAGAAATACTTA | 5521 |
rs111976184 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725802 | AGAATTTATCACATG[C/T]ACTTACTATCCACTA | 5521 |
rs111987540 | in-del | -/ACACAC | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915448 | TCATTCTACCTATGT[-/ACACAC]ACACACACACACACA | 5521 |
rs112010037 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747062 | AGTACCTACAACAGT[G/T]CTTGTCACCTTCTAG | 5521 |
rs112010503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936328 | TGGTCATTCATGCTG[C/T]CTAAGAAGATGCCTA | 5521 |
rs112024166 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037169 | TCAGGGAAAAAAAAT[A/T]ATTTTTGCCTAAGAT | 5521 |
rs112042148 | snp | C/T | 0.292266 | 0.246401 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730126 | CTTACATCAGTGTGA[C/T]CTGGATATGAGACCT | 5521 |
rs112048876 | snp | A/C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623121 | GGGCAAGCAACAGTA[A/C/T]GTTGGATTAACACAA | 5521 |
rs112082877 | in-del | -/C | 0.283158 | 0.247791 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737808 | GGCCAGGTGTGGTGG[-/C]TCACACCTGTAGTCC | 5521 |
rs112088007 | in-del | -/TTCTT | 0.21875 | 0.248039 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681925 | TCTTCTGTAATGTGA[-/TTCTT]TTCTTTTTCTGACAC | 5521 |
rs112091481 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653845 | TTGCTCAGATAAGAC[-/A]GGGGGGATGGAGAGC | 5521 |
rs112106372 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805883 | TAATTATCGGCAGCT[C/T]GATGAGTCTGACTTC | 5521 |
rs112118207 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704305 | AGACAAAATAATTTT[A/G]TGATATGGTAAGAGG | 5521 |
rs112131195 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897852 | GGCAAATTTATTTTT[A/C]AATTATTAGAAGGTT | 5521 |
rs112131786 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626018 | AGGAAACATTCCCCC[C/T]TAGAGCCTCTAGCAG | 5521 |
rs112134373 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050825 | ATGATGTTATTTTTC[A/C]CTCTGTGTGTGTGTG | 5521 |
rs112137526 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910296 | CTATACAGCTATGGA[G/T]GCAAAAGCTAGTTTG | 5521 |
rs112137616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959648 | ATGGAAAGGTTTCTG[A/G]GTCCTTGAAGAGGTG | 5521 |
rs112147131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644438 | TAAGATTTTTGGTCA[C/T]TTTATTTTCCCCAAA | 5521 |
rs112156369 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899698 | TTAGGAAATTATTCT[A/C]TGAAGACTAATATCC | 5521 |
rs112179619 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767198 | GAATACTTGAGAATA[C/T]ATAAAAGTGGCTCAT | 5521 |
rs112195430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803043 | ACAGGGACAAGAGGA[A/G]TGAAATTCAGCTTAT | 5521 |
rs112204686 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602735 | AGCCCTGATCAATCA[A/G]AATTGAAATTGCAAA | 5521 |
rs112204975 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617840 | GCTGGGATTACAGAC[A/G]TGTGCCACCACGCCC | 5521 |
rs112207199 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900984 | TTTTTATGGCTGCAT[A/G]GTATTCCATGGTATA | 5521 |
rs112226906 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902265 | GAGTCCCTATAGTAG[A/T]CAAACAGCAAAATAT | 5521 |
rs112228988 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668389 | CTTTCAATCTTCTTT[A/G]GGCAATGAACCCATT | 5521 |
rs112236387 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068797 | TCAATATTTGGAAAT[C/T]ATTACTGCTTGAATA | 5521 |
rs112239088 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080418 | TTCTAGTTCCTTCCA[A/C]TTGCCTATCATCCAG | 5521 |
rs112240444 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065195 | AAGTGTATGATGGAG[A/G]ACATTCAGGACCTTC | 5521 |
rs112248308 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625819 | TAAGGTGGGGAGAGT[A/G]TCTTGGATTACCCAG | 5521 |
rs112251256 | snp | A/C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752448 | CTCAGAACTTAACAC[A/C/T]TATCTGAAATTATCT | 5521 |
rs112255011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809200 | GCCTTCTATGTGGCC[A/G]TCAGGCTTTCTGCTT | 5521 |
rs112258257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732415 | CAGAGCAAGTGAAAA[C/T]CAATGGGAGGATGGA | 5521 |
rs112266390 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753585 | GAGGGAGATTCTTGC[C/T]AGCCAAGGACACTTG | 5521 |
rs112272121 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737961 | CAAAACAAAACAAAA[A/C]AAACGTTGTTAGAAA | 5521 |
rs112286767 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005995 | CCGAAAACACTGAGG[C/T]CACTGACAACCCATA | 5521 |
rs112287761 | snp | A/T | 0.0626037 | 0.165477 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063101 | GGAAGGGAAGGGAGA[A/T]AGAAAAGAAAGACTA | 5521 |
rs112292020 | snp | C/T | 0.282105 | 0.24793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749877 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 5521 |
rs112294574 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676996 | CCAAGTGTGGCTTTG[C/T]TTTGTCACTTCTATC | 5521 |
rs112296827 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718004 | TTAATGCATCTACCA[G/T]AATTCATCATTATGT | 5521 |
rs112308435 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875103 | AGACAAGGTTTTCCA[C/T]TGAATGTGTGACTTT | 5521 |
rs112312077 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749852 | ATCTGCCTGCCTTGG[A/C]CTCCCAAAGTGTTGG | 5521 |
rs112314106 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679791 | CAAAAAACACATGAA[A/G]AAATGCTCATCATCA | 5521 |
rs112321659 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829377 | ATATGCTTAAGCATA[G/T]AAATATTAATGGGCA | 5521 |
rs112323270 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810787 | GTGTGGGTTTGTTAC[A/G]TATGTATACATGTGC | 5521 |
rs112330766 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759715 | CATATATTAATGAAG[C/T]GTCCATATGGGTGGG | 5521 |
rs112335142 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935839 | TAACTTTTGAGGTCT[A/G]CATATGCTTGGACTC | 5521 |
rs112340674 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000089 | ACTTTAACAGACAGA[A/G]GGATTCCAAGAGGAA | 5521 |
rs112342262 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708357 | CAAAAAAAAAAAAAA[-/A]CACTGTATATCTGTA | 5521 |
rs112363900 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956772 | AAGTCCAAGATCAAG[A/G]GGCCAGCAGATTTGG | 5521 |
rs112378337 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780322 | AAAATGGGCAATGTT[C/T]ATATGGTCAGAAAAG | 5521 |
rs112406705 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618976 | ACTCTGTGTGGCTGA[G/T]AGCCAACAGTCCTAC | 5521 |
rs112412348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844630 | TTTTGAAAACAAATT[C/T]AAGATTCCATGCAGA | 5521 |
rs112426414 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862434 | TCTTTAGATCTAGCT[A/G]TCTGAACTTGGACCT | 5521 |
rs112451133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809869 | GCTCTGTCTGTAGTG[C/T]AGGTGGGAAATGGCA | 5521 |
rs112457307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833424 | CAAACAAAGCTCTTA[A/G]GCTGCCTTGAAACAA | 5521 |
rs112459500 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907706 | GTCAAGGCCCAGCTA[A/C]GTTTTTGTCTTTTCC | 5521 |
rs112470770 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589810 | CTGGGAATGTTGGAC[C/T]CCTTTTAATTCTATT | 5521 |
rs112475080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008402 | AATTCATAAAATATT[C/T]ATGAAACACCTTATG | 5521 |
rs112482796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947294 | TCATTATTCTACCTG[C/T]ATGTGCTTTGCGCCT | 5521 |
rs112496048 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783991 | CACGTAATTCCCAGA[C/T]CTACAAAACTTGGCA | 5521 |
rs112504027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879470 | ATTGCAGCCTCTCCG[C/T]TAGGTTTTGCTTGTG | 5521 |
rs112524835 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639656 | ACTCCCACTTTTCCT[A/T]GATTTTCCTACTCGT | 5521 |
rs112527999 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934583 | GGTAGTTTTTCATAA[A/G]AAAAAAAAAAAAAAA | 5521 |
rs112530787 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049162 | AGGAAAGGATTCTCT[A/G]GTGAAGAAACATTTG | 5521 |
rs112535434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919804 | TATGCCAGAATAGCA[A/G]CTTTACAGGTGAAAA | 5521 |
rs112542388 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689857 | CAGAGGAAACAGAGT[C/T]GCCAATGCTTGTGAG | 5521 |
rs112556623 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707284 | TGCTGCTCCAGGAAC[C/T]GTACCTTGTCGACGA | 5521 |
rs112561064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898088 | TACTCAGGAGGCTGA[A/G]GCAGGAGAGTCTCTT | 5521 |
rs112581066 | snp | A/G | 0.32955 | 0.237006 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843119 | TTGAACCTGGGAGGC[A/G]GAGGTTGCGGTGAGC | 5521 |
rs112582641 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608098 | CAGACTTGGCTGTAT[A/G]CCATAGTTTGCTGAG | 5521 |
rs112604521 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639699 | TGATTTTTGCCCTAT[C/T]TGTGCATCATCAGAT | 5521 |
rs112613179 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822131 | TCCTAAATATGCTTA[C/T]TTTACAAGAAAAGAA | 5521 |
rs112613922 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804005 | ACCCCGTCTCTACTA[A/G]AAATAAAAAAAATTA | 5521 |
rs112645592 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706776 | ACTTGATCTGATACA[C/T]GCTCTCGGCCTCAGC | 5521 |
rs112667932 | snp | A/G | 0.244205 | 0.249933 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617746 | GTCACCGAGGCTGGA[A/G]TGCAGTGGCGCGATC | 5521 |
rs112670376 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777909 | TGCACTGTTACGAGG[G/T]AGTAAAATTCCCAGC | 5521 |
rs112679860 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002046 | TATCCTGACCCTTGC[C/T]TCCTGGGTCCTAATG | 5521 |
rs112685369 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902099 | CTTACCTAAAGACCT[C/T]ACCATGTGCACACTC | 5521 |
rs112688576 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734723 | GTCAAATTGGATAAA[A/T]TCAATGTCTACCTCA | 5521 |
rs112692649 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693004 | TTCCTCTGTCTTGCA[C/T]AAGGTAGGGTTTGGA | 5521 |
rs112692780 | in-del | -/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724316 | GGGGACTGTCATAGG[-/T]TTTTTTTTTTGAGGG | 5521 |
rs112694325 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709027 | TGCCACATGCTTGCT[A/G]TCCTTGACCTACTGT | 5521 |
rs112694688 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728308 | CCACTGTGTGACTCC[C/T]ATAAACAGAATATTT | 5521 |
rs112698243 | snp | C/T | 0.386504 | 0.209444 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003894 | GTCCCCCAACTCACT[C/T]GAGGGTCAATTGATT | 5521 |
rs112708135 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730139 | GACCTGGATATGAGA[A/C]CTGGAGTCAAAGGAG | 5521 |
rs112735259 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912286 | GAGAGGTACAGCATA[A/C]CCTAAAGAGAGTGAC | 5521 |
rs112736939 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602841 | CAGCTTTTGGGCTTC[A/G]GCTGAGTATTAGTGA | 5521 |
rs112741081 | snp | A/T | 0.0475351 | 0.146656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967369 | TTGAAGATTTTATTA[A/T]GTGCCAGGCAGGGTT | 5521 |
rs112742591 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984652 | TAACTTTTAGAGGAA[A/G]CTTCATACTGTTTTC | 5521 |
rs112749607 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082384 | CTCTGACTTGGGACA[A/C]GTTTCTAAGCATAAT | 5521 |
rs112763274 | snp | A/C | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078552 | CAGCACTTTGGGAGG[A/C]CAAGGCAGGCGGATC | 5521 |
rs112779596 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763057 | CTGTTTTGCTAGATT[G/T]CTGCCTGGAGCACTT | 5521 |
rs112782562 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671945 | GGACTAAGAATTAAG[C/T]TAAACGATAAGCAAA | 5521 |
rs112784873 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897874 | TAGAAGGTTAAAATA[C/T]ACTGGTCAAGGAAAT | 5521 |
rs112798895 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913142 | GAATGAGTTTATATT[C/T]GGCGGAAATAGTCTA | 5521 |
rs112806158 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951363 | CTTTTTTTTTTAAAA[-/A]TTAAGTTCCAGTGTA | 5521 |
rs112821509 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645735 | GGTCAAAGTTGAAGT[A/G]TCCCTAGAGTCCAGC | 5521 |
rs112842915 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694281 | TGGCTTGCGCTGGAG[A/C/G/T]GAAAGGAGATCCTGC | 5521 |
rs112845004 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710794 | AAATGAGAAAGTTCT[C/T]ACATCTGTGGGGGAA | 5521 |
rs112847920 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690973 | CTTTCCTGCTTCTCC[A/G]TCTGCCACCAGAGAG | 5521 |
rs112853057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951280 | AATTATTATACCCAT[A/G]TAACCAGTAACCACC | 5521 |
rs112863419 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708698 | CTCAACTTGATTTGG[A/C]ACCAATAATTATTTT | 5521 |
rs112893364 | in-del | -/AC/ACACAC | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767539 | AATACACACATACAT[-/AC/ACACAC]ACACACACACACACA | 5521 |
rs112894460 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711522 | AAAAGCCTTTGCAGC[A/G]CTGTCAGGGATTCAG | 5521 |
rs112916527 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871438 | AGTGACATGGAGAAA[G/T]CTATTCAAAAAACTC | 5521 |
rs112917512 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732597 | TGGTAAAACATATTT[G/T]TACCACAAACAATAA | 5521 |
rs112942402 | snp | A/T | 0.246485 | 0.249975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903543 | CGGGACTATAGGTGC[A/T]TGCCACCACACCTGT | 5521 |
rs112942608 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677046 | CTCCTGAACTCCTAT[C/T]TTTGTTGTCTGCTTT | 5521 |
rs112945943 | snp | C/T | 0.0614824 | 0.164198 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912063 | GGCAACAAGGTGAAA[C/T]CCTGTCTCTACTAAA | 5521 |
rs112961103 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861824 | TTTATCATGGATGAA[A/G]CTACCTTTGACTTTC | 5521 |
rs112972925 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683701 | CCCAAACTCTCATCC[C/T]CCAAAGGCGAAACAT | 5521 |
rs112985608 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038166 | AGAAGTTATTGAGCT[C/G]TATTATTTGAACACT | 5521 |
rs112989178 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609659 | CGCGAGCCGAAGCAG[C/G]GCGAGGCATTGCCTC | 5521 |
rs112998873 | snp | A/G | 0.0652541 | 0.168602 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063274 | AAGAAGAATTTGCAC[A/G]TGTGAAGATATAAGT | 5521 |
rs113001941 | in-del | -/A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991061 | TATCATTAAAAAGAT[-/A/T]AAAAAAAACACAAAT | 5521 |
rs113004867 | in-del | -/AGTG | 0.236434 | 0.249632 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685199 | AATAGTCCTAATAAT[-/AGTG]AGGAACAGGAGCTCT | 5521 |
rs113018230 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978503 | CTTTTATGATTTTAC[A/G/T]TACTACGTTTAAGTC | 5521 |
rs113018648 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680732 | TTAACAGTTTTCTGG[C/T]AAAAAGAAAATAAAC | 5521 |
rs113022747 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918232 | CAGGAGGAAGAATAT[A/G]TATGAAGGGAAACTC | 5521 |
rs113030390 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725472 | CTAGGATATGCATGC[A/G]TGCATCTAAATGTTG | 5521 |
rs113045853 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769448 | TCCTACATGTTTATC[G/T]TAAACTATAATCGTT | 5521 |
rs113062175 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811789 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 5521 |
rs113098407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677612 | GGCCTGATCTCGGCT[C/T]ACTGCACCAGGCTCA | 5521 |
rs113109890 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687122 | GGAGAGAGAGGGAGC[G/T]ATTGATCGATTAATC | 5521 |
rs113112383 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726767 | ACAAAGGATTTCCCA[C/T]AGTCTCTTTTGCTGT | 5521 |
rs113116286 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956907 | TTGAGGGCATTAATC[C/T]CATTTATTAGGATTC | 5521 |
rs113122413 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055108 | CATTAACTTAGGACC[C/T]CCAGAAACCACATTT | 5521 |
rs113124572 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999235 | TTCTACAGTAGAATA[A/T]AGATATTGATTAAAT | 5521 |
rs113126770 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718184 | TAGTAGACATGCAAG[C/T]ATTGTTCAAGGAAAG | 5521 |
rs113130825 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624603 | GCTTCATTCTTAAAT[A/G]GCCACAGAGTGACAT | 5521 |
rs113138538 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817170 | TCTAGAGTGTCAAGA[A/T]CTTTCTTTTCTGCCT | 5521 |
rs113139604 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650811 | TCATTTATTATCACA[C/T]ACAAAATAATAGCCA | 5521 |
rs113149104 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592637 | GGCATTAATCTGAAC[C/T]GTTCAGGCTGGAATT | 5521 |
rs113152487 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834063 | CTATGGATTGTCTAA[C/T]GATTCTTTGGAAAAA | 5521 |
rs113176269 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877217 | CCCTTCCTGCCCGCA[A/C]AGCACTAGTGCTTAT | 5521 |
rs113179865 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903247 | TTTAACTGTCAATAG[A/G]CATTAACCACATTAA | 5521 |
rs113179897 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615675 | AAACCAAGGATTTAA[C/G]TTACTTACCCAGAGA | 5521 |
rs113185754 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628273 | TTTAAGGTCTAAAGT[G/T]CTTATGCCATTTCCC | 5521 |
rs113193245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785651 | CAAAGGCAAGCAACG[A/G]AACTAAAATAATAAC | 5521 |
rs113201475 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635840 | TGTCAGGGGTTCATA[A/T]AATGTGACCAAGTCA | 5521 |
rs113207618 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593247 | GGATGGGTTGATGAG[C/T]TTCTCATGTAGATGA | 5521 |
rs113208019 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661726 | TAAACTCGCTAATTA[C/G]CAACTCATGCAGAAA | 5521 |
rs113208133 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607227 | CCACAGAGGGTAAGA[A/C]CTCCCTCGGACTGAC | 5521 |
rs113215186 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658287 | TGAGGCACTAGACGG[G/T]AAATCTCTCAGAGGG | 5521 |
rs113230546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820058 | AATTGTGGTTACCAG[A/T]AATAGGGGATTGGGA | 5521 |
rs113231233 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768814 | TCTGCCTAGTGTTTC[C/T]GAGACTTTTTACAGC | 5521 |
rs113236954 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623719 | AGAGAAGATAAAGGC[A/C]AGTATCATTATGAGC | 5521 |
rs113241401 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625956 | ACAATGGAAGAAGGG[A/G]CCATTAGCCATGGAA | 5521 |
rs113246089 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018882 | CAAACTCAGAACAGA[A/T]GATGATGGTGGTTAT | 5521 |
rs113254633 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837088 | GACAGTTATGACTTA[A/G]GGTGATTTGATTTAG | 5521 |
rs113271756 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016552 | AGTCTGAGAAAACAT[A/T]GGGGACACAGTCACA | 5521 |
rs113284022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900135 | CCCTTCCTTTGCTAG[A/T]TGCTTTATTGTGATT | 5521 |
rs113284985 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890824 | GCCCTGAGCCATGAC[A/T]TTAACATTTTAGGAT | 5521 |
rs113291911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947743 | CACCACTGTCCTTTC[A/G]CATCTCACCATCTAC | 5521 |
rs113297340 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616041 | GCATAAAAACAGACA[C/T]ATAGATCAATGGAAC | 5521 |
rs113311931 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811717 | AGGCGCCCACCACCA[C/T]GCCCGGCTAATTTTT | 5521 |
rs113329996 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813630 | ATAAAACACCTCCTT[C/T]TTAAGAGCTCCATCT | 5521 |
rs113342083 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689799 | CCAGAATGATAAGGT[A/G]GACTTACATGGAGGT | 5521 |
rs113348020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828479 | TGTACTGCTTTCTTT[A/G]TAATGAGTTTTTATG | 5521 |
rs113351243 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788685 | GCAGTGGTCCGAGAT[C/T]GTGCATCATTGCATT | 5521 |
rs113365956 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615437 | CAGCGCACCAGCATG[G/T]CACATGTATACATAT | 5521 |
rs113369917 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880225 | TGTGTGTGTGTGTGT[A/G]GTGGGGGGAGTTCAG | 5521 |
rs113372374 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898244 | GATATGCAGCATTAT[C/T]TCTGAGGGCTCTGTT | 5521 |
rs113399820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817906 | CTCCCATAAAACACC[A/G]TCCTCCCATTTGCTC | 5521 |
rs113403519 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625498 | ACTGTCCTAAATGCT[A/G]AGGGGGTTTGAGAAA | 5521 |
rs113403921 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814823 | TGGAAAAACCCCAAG[A/T]CAAAAGTCAAACTGC | 5521 |
rs113404347 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787627 | GGCTGGAGTGCAATG[A/G]GGTGATCTCAGCTCA | 5521 |
rs113404594 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785592 | CTTAATAGCTTAAGT[G/T]GGTGAAACAAGAAAT | 5521 |
rs113405259 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878378 | GGTGCCAAGATACGC[A/C]GTGCCCCGAGGGGTC | 5521 |
rs113412098 | in-del | -/AA | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818356 | GCAAAAAAAAAAAAA[-/AA]TCACGAGGATTTTTA | 5521 |
rs113413992 | snp | C/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690147 | TTTAGCAGAGCTGCT[C/G]GTGTCTGAAATCACA | 5521 |
rs113415392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689268 | AGTGACTATCATCAT[C/T]CCCGTTATATAGATG | 5521 |
rs113422020 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067681 | ACTTTCTCTGTCTAT[A/G]AGTGGGCAGATCTTC | 5521 |
rs113428906 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897120 | GGGTCATTAAGTGAA[C/T]GATGCATTTCATGTG | 5521 |
rs113436582 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770003 | ATTATTTATACTAGC[A/C]AAAAAAATCAGAAAT | 5521 |
rs113449122 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975593 | TCATGCTGTTTTCCA[A/T]AGTGGTTTCACCACT | 5521 |
rs113450437 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978596 | TGCATATGGCTAGAC[A/G]GTTTTCCTAACATCA | 5521 |
rs113484818 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005776 | GACAAAGAGGGAGTC[A/T]GAAAGAGAGAAAGAG | 5521 |
rs113489827 | snp | G/T | 0.0535932 | 0.154675 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599770 | CGTCATCTACATTAG[G/T]TATTTCTCCTAATGC | 5521 |
rs113501900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637298 | GTTTTCACCAAGAGG[A/G]TATTTCACAGTGTCT | 5521 |
rs113502573 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906397 | GCGCGATCTCGGCTC[A/C]CCGCAACCTCTGCCT | 5521 |
rs113503010 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726800 | AAATTATCCAAAGTC[G/T]CTTATGTTCATAAAT | 5521 |
rs113505349 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691743 | TGACCCCCCTGTCCA[C/T]CCTCTCCCTGCTCAC | 5521 |
rs113512318 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651180 | GGCTTTGGAAGCTAT[A/G]CCCCTTCCTGGCTTT | 5521 |
rs113519932 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806720 | CTAGCAGTCACCAAC[A/C]AGGATAGTATGAATG | 5521 |
rs113520589 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727874 | CCCCTATCTCAACCC[C/T]CAACTCCGAAAACCA | 5521 |
rs113531536 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865751 | ATCTCTAATCTCCAG[A/C]TCACTTGTTAAAACA | 5521 |
rs113531608 | in-del | -/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711234 | AGATGCTTCTCAATC[-/T]TTTTTTTTTCTATGC | 5521 |
rs113537602 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911693 | TGTCTTCCTCATAGT[A/G]AACCCAAATACCTCT | 5521 |
rs113540351 | snp | A/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065697 | AAAAGAGGGAAAATG[A/T]CATATGACTTAGTGA | 5521 |
rs113555722 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934944 | AGATGGGAAATTATC[A/C/G]CTTTTCTACTGCAAA | 5521 |
rs113565190 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877846 | GAGCCCGGATGGATG[A/C]GAGGTGCACTGGGGC | 5521 |
rs113566075 | snp | G/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861856 | TTAAAATACAGCATT[G/T]TTTTTTTTTTTTTTT | 5521 |
rs113571347 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042734 | ATGTCAAGTAGTAAG[-/A]AAAATCTAGGCAGTG | 5521 |
rs113572042 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681068 | AAATGCTTACATCAA[C/G/T]GCATCAGTCGAAGCC | 5521 |
rs113591361 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648717 | TAATGGGAAAGAGTA[C/T]CTCTGGGGCCTGAAG | 5521 |
rs113597659 | in-del | -/GGTC | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869940 | CACTGTGGTAGGGTC[-/GGTC]CTTCCTGGTGGTATT | 5521 |
rs113611185 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810944 | TGTTCTCATTGTTCA[A/G]TTCCCACCTATGAGT | 5521 |
rs113624276 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642598 | TAACAACAGTTTGAT[A/G]ATGTCATTTAAAACT | 5521 |
rs113628038 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779416 | GCGTGCGATTGGCAT[C/T]TGCAGAAGCCTTGAC | 5521 |
rs113643421 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988673 | AATATTAAAAAGATC[C/T]GAAATAAACAACCTA | 5521 |
rs113645809 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059483 | AGAGGAATGGTGTCA[C/T]TATAAGGAGAAGGGA | 5521 |
rs113645813 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706249 | CAGCTTCCCATCTCG[G/T]GTCTTGATCTTCTTC | 5521 |
rs113664188 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865510 | TCATATTCATATTCA[C/T]GTGTGTTTTTTAACG | 5521 |
rs113679616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944602 | TGTCCCATGATTTAA[A/G]GAGAAAAAAAAAGGA | 5521 |
rs113681816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045554 | ATTTCCATCATTAAG[C/T]GATGCATGACTGAGT | 5521 |
rs113689301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810133 | CTTGTGAAAGTCAGG[A/T]ATTGTTACTAACATC | 5521 |
rs113694541 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931807 | CAGTGAGTTGACTAT[A/C]AATGGAAAACACTTC | 5521 |
rs113703657 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838359 | GGTAGATCTCTTGAG[A/G]TCAGGAGTTCAAGAC | 5521 |
rs113712765 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015584 | GCCTTCTCTGAGTCT[C/T]ACGGTTGGCTGACTC | 5521 |
rs113716354 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724261 | TGATCCAGTGTATTC[A/G]ATGGCCATCCCAAAA | 5521 |
rs113716753 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741036 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT | 5521 |
rs113721402 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757382 | GATAGTACTGGCTGC[C/T]ATGTAGGGTGAGGAT | 5521 |
rs113724945 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005777 | ACAAAGAGGGAGTCA[C/G]AAAGAGAGAAAGAGA | 5521 |
rs113733209 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596030 | TTTCTCCAAAGGGCC[A/G]GATAGTAAATATTTT | 5521 |
rs113738282 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727009 | GATTACTGAATGCTA[C/G]GTTTCATCCTATAGA | 5521 |
rs113740530 | in-del | -/T | 0 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597136 | TCCTTCTTTCAGCCA[-/T]CAAAAGTTCTGAGTC | 5521 |
rs113761022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855677 | CAGGGTTCATACAAA[C/G]TCTGTTACAAACTCC | 5521 |
rs113774119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810901 | ACAACAGGCCCCAGT[A/G]TGTGATGTTCCCCTT | 5521 |
rs113783234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698552 | CGTAAATACTTACAT[C/T]GACCCCTTAAAGAGA | 5521 |
rs113784016 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626851 | ACTACTAATGAATAA[C/T]ACTCACTTCCAAAAT | 5521 |
rs113806287 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737751 | TTATGGTGGGTGTCA[C/T]GGTCTTCTTTGAGTG | 5521 |
rs113825755 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715431 | TTTCTTTGAAACTAC[A/C]ATTTATTGAGTTGGC | 5521 |
rs113842851 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595125 | CTCACTTCCAAACAG[G/T]TCCAGGCCTTGTCAG | 5521 |
rs113847944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858064 | CTGGGACTGTCATGA[A/G]CACATTACAGGCACC | 5521 |
rs113849381 | snp | G/T | 0.396182 | 0.202807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692770 | CGATCTCCTGACCTC[G/T]TGATCCGCCTGCCTC | 5521 |
rs113850632 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978686 | CATGGTTGTAGATGT[G/T]TGGTGTTATTCCTGA | 5521 |
rs113853909 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704323 | ATATGGTAAGAGGAT[A/G]TAGTAATAAGGTAGC | 5521 |
rs113861141 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750845 | CAGTTCAAATACACA[C/T]GTTGGTACGCTGGAT | 5521 |
rs113879396 | snp | A/C | 0.0618563 | 0.164627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755480 | CACCTTAGCATAAGT[A/C]ATATATAATAAATGA | 5521 |
rs113892101 | in-del | -/TTAA | 0.491629 | 0.0641526 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827435 | CCCAGAACACATCGG[-/TTAA]GTTATTTTCAAAATG | 5521 |
rs113894135 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069905 | AAGCAATTCTCTTGC[C/T]TCAGCCTCCTGAGTA | 5521 |
rs113906847 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897380 | TCTTCCTTTTGAAAG[A/C]AAACTAAAATGGTCT | 5521 |
rs113909217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955690 | AGGTGTCCTGATTTA[C/T]TTCTGCATGGAAGAG | 5521 |
rs113917217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730058 | AACCCATGAAAGCAG[A/C]CAGGAGGGAGGCTAT | 5521 |
rs113920751 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629604 | GCACCATCTCATGGT[C/T]TCCCATCTCACTTAG | 5521 |
rs113925240 | in-del | -/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714802 | TAAAAGACCTCTTGA[-/T]TTTTTTTTTTGTTTC | 5521 |
rs113928961 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782163 | AGATGCTAGCATCAC[A/G]CTTCCTGTACAGGCT | 5521 |
rs113935576 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742155 | ATCTCAACAGCCGCC[A/G]GGGGGAACTTTGCTG | 5521 |
rs113940146 | snp | G/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060445 | CAGCCTGGGCAATAG[G/T]GTGAATACCCACCTC | 5521 |
rs113946293 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733159 | GGAGGTGCTGTTCCC[A/G]CAATCTGGTTACTCA | 5521 |
rs113949012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991612 | AAATGAAAAATGTTT[A/G]AAGTAATGGATATAA | 5521 |
rs113955839 | snp | C/T | 0.00414544 | 0.045338 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055646 | ACCCACCCAGACACT[C/T]TCCCTCTCTGGTCTG | 5521 |
rs113978560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648113 | ACATTTCCTAGGCTG[C/T]CTTGCAGTTAAGAGT | 5521 |
rs113979436 | snp | C/T | 0.5 | 0 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691177 | CGGCCCTCCTCATCT[C/T]TCAGATTGTAGCCTT | 5521 |
rs113985427 | snp | C/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847474 | AACTTCTACTCTATT[C/G]TCAGCTTAAGGTTAG | 5521 |
rs113986773 | snp | C/G | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675510 | GGCAACAATAACAAC[C/G]ATGATTGTTATGGCA | 5521 |
rs113994699 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966938 | AGAATTGATCTTTCA[A/G]TTTCAACAAGCATGG | 5521 |
rs114000346 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640693 | ACTGGAAGGGATCTT[C/T]GCTGTGTGGGAGGGG | 5521 |
rs114000925 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946417 | TTCTGGGGTGTAAGT[C/T]AGAGTCTTTCATTGC | 5521 |
rs114001736 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910273 | GCAGATAGAAAAAAA[A/T]TTGAAGGCTATACAG | 5521 |
rs114003542 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881871 | TTCATATTAAAATAA[C/T]CTGTTGTGAGCTGGA | 5521 |
rs114005943 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874513 | GTATTAGGCATATCC[A/C]GAGTGCTTGAGTGCT | 5521 |
rs114008868 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637213 | ATACATTGTAGATAC[A/G]AGAATATCATGCAGT | 5521 |
rs114030740 | snp | C/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082596 | GCACTGTGGTAAGCA[C/T]TTGACTTAGAGTAAC | 5521 |
rs114043211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067911 | CTTCCACTTGCTCTG[A/G]CATCGTGTCTGTAGA | 5521 |
rs114056996 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022455 | GTCCCAGCCATTCGG[A/G]AGGCTGAGGCAGGGG | 5521 |
rs114061965 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792280 | CCAAAAAATTACTGG[C/T]CAATACAGTGACAAA | 5521 |
rs114063718 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724788 | TACAAAAGCAAGTCT[A/G]TCTGGGAGTTACATG | 5521 |
rs114066953 | snp | C/G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889551 | GGTTAATGGCAGGGG[C/G/T]GTAATGCATGAGGTC | 5521 |
rs114077101 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822654 | TCTCCATACCATTTA[A/T]CAACATATAAAATTC | 5521 |
rs114083027 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064058 | GAGGACCTTCCCCTG[C/G]GCGTGTCACACTGCT | 5521 |
rs114086130 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823023 | GGAAAGCTGAGTCTT[C/T]TGGCAAAAGGGACTG | 5521 |
rs114091749 | snp | A/T | 0.0482946 | 0.147699 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766114 | TCTTGAAAAGCCCTC[A/T]TTATACTTTCTGTAA | 5521 |
rs114105967 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791843 | CTTCTGCCAATAATC[C/T]CCTGACTTTCCCTTT | 5521 |
rs114107651 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933432 | AATGATTATTAGGGA[G/T]TTTTTATTCCCATTC | 5521 |
rs114116750 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620552 | GCGCTCATATTTGGT[C/T]TTTCACTCTCTGCAA | 5521 |
rs114119550 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625080 | GCAACAATAAACATT[C/T]GTTGAATAAATAAGT | 5521 |
rs114127817 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641146 | TTCCATGTGTTGTCC[C/T]CCTTGCCCCTCATCT | 5521 |
rs114128160 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954710 | TTTAGAGAAACACAC[A/G]CACCAGTACATATGT | 5521 |
rs114140461 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818663 | ATAGTTTCATTTTTT[C/G]TACTTTACAGATGAG | 5521 |
rs114144469 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757073 | TTCAAAACACATGGG[C/G]AAGAACAGTCCTGGT | 5521 |
rs114159643 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963230 | AATCAGTGCAGACAA[A/T]CATTGCATGAGATTT | 5521 |
rs114164448 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055374 | TGACTTGTTTGCATG[C/T]TAAATGAAACAAGGA | 5521 |
rs114171756 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809645 | AAGCAAGGAGTGGGC[C/T]ACGAGGCTGTGGGCA | 5521 |
rs114184521 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916401 | AATGCTGGGCAGAGA[A/G]TGACAGAGAGAACTA | 5521 |
rs114196162 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924482 | CTGGAGATTTTAAGT[A/G]CAAGGATAAGAAAGG | 5521 |
rs114200239 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835869 | CTAATTCTGCATCAA[A/C]GACATCTTGGACATT | 5521 |
rs114201187 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980097 | AGATTTATATTTATT[G/T]TTATGGAGAGATGCC | 5521 |
rs114212149 | snp | C/T | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146878996 | CTCGCGCCACTCAGC[C/T]AAGGGCCACGTCTAC | 5521 |
rs114215777 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646718 | TCCAGATAATAAAAT[C/T]AGCAGAATAAAAGCT | 5521 |
rs114215987 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990944 | CAAAAGAAGGTATAC[A/G]AATGGCCAACAGGTA | 5521 |
rs114216530 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664280 | AAATTAGAGACAATC[C/T]GCTCAAGCACTGTTG | 5521 |
rs114218768 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727971 | AGTGAGATCATGCAG[C/T]ATTTGTGTGCTTGGA | 5521 |
rs114221907 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719993 | ACATTTCCTAGTGTA[C/T]CCCCAGCCTTAGTGT | 5521 |
rs114223999 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632375 | TTCCAGCCTCCAGAA[A/C]TTTGAAAAAATAGTT | 5521 |
rs114231002 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750742 | GCACAGCATTGCTAT[A/G]GCTTATATATTTTCA | 5521 |
rs114236469 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737151 | AGCCACATTTCAAGG[A/G]TTCAGTAGCTACTGG | 5521 |
rs114236760 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901380 | TGTTGTGACATGCAC[C/T]TATCATCCCAGCTAC | 5521 |
rs114238462 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059040 | GACAAGTTTGGGTAA[C/T]GGAAAGTTTTCCAAA | 5521 |
rs114239630 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794112 | CAAAGACCAATAAAA[C/T]TGGCCTTTATCTTAA | 5521 |
rs114246824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858661 | GTTGGTGATGATCAA[C/T]CCATTGTTTTTCTTA | 5521 |
rs114249040 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061656 | CTCTCTTGGCATGTG[A/G]CTAAAGCAAGAGAGA | 5521 |
rs114256827 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990282 | TACCAAATAAATTTT[A/G]AGCAAAAGCAACAAA | 5521 |
rs114261747 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997766 | AAAGTAGATATTTCC[A/G]CAAAACCTAGCAACA | 5521 |
rs114262212 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847244 | TGCCTGTAGTTGTCC[A/G]CTAACCCCAGGATAA | 5521 |
rs114263530 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937759 | GGTTATCTGCAACAA[C/T]AGAGGGAATGTGTGG | 5521 |
rs114265792 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776658 | AAAATTGGACTTCAC[C/T]GAAATAAAAATTTCT | 5521 |
rs114284946 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851685 | TAGGCAAAACACAAG[G/T]TATACCTTTTCTAAG | 5521 |
rs114286205 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830358 | GTTAGGATTTCAATC[A/G]TAGTCATATCCACTC | 5521 |
rs114287763 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629736 | CCCTCCCTCTCTTCC[C/T]CCCTTCCTCCCTCCC | 5521 |
rs114290362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945508 | ACTGTCCAAGTCCGA[C/T]ATATTGACTACCTTG | 5521 |
rs114293330 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810533 | AACCATACCAGATGC[A/G]GAAACTCAGATAGAG | 5521 |
rs114310193 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972239 | ACACTTCACAGGTAA[A/G]GTTCCCTCCTCATGT | 5521 |
rs114318763 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023681 | CAGTTTGAGTGGGTT[A/G]AGGGATACACAGATA | 5521 |
rs114322584 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926735 | AGCTCCCCTGAGTCT[A/G]ATATCTGCTGGACCT | 5521 |
rs114326457 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827860 | GGGATCATGGAGAAA[C/G]AGGGCCCAGAAATAG | 5521 |
rs114339387 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758618 | CACAAACTTTGTCTG[A/G]TTTTTCCCCATCCTG | 5521 |
rs114339959 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744488 | TGGGACTGAAGAGAG[C/T]TTTCAGAATGAACAA | 5521 |
rs114352803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957737 | GCAATAACGTTCTGA[C/T]CTATGGTAACACTAT | 5521 |
rs114362206 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725325 | ATATAGTTTTATTGC[A/G]AAAATGGAAAGTAAA | 5521 |
rs114370352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884414 | TAGACTTGTGAGTAA[C/T]TGCTTTTATAGGGCT | 5521 |
rs114372593 | snp | A/C | 0.029116 | 0.117091 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717793 | TTTCAGGATCTCATA[A/C]ATTTCCTGCTTTCCC | 5521 |
rs114381165 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777454 | TATAGTAGAGGTTAC[A/C]AGAGACTACGGAAAG | 5521 |
rs114393201 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790125 | CTTCGGGACTGCTCT[A/G]TGTATGAATGTAAAA | 5521 |
rs114393556 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783124 | TAGGTTAAACAAATT[A/G]AGATTAATGTCATGG | 5521 |
rs114395619 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763735 | AGTTAAGACAAGGAC[C/T]CTTCTTTCCAAAGGT | 5521 |
rs114411985 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842036 | TCTGAGACAGGGATT[A/C]ATCCATACTCCCTAG | 5521 |
rs114417860 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708215 | AAAAAAAATTAGCTC[A/G]GCATGGTGGTGTATG | 5521 |
rs114419691 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041409 | GCTATGCTCTCTCCA[A/G]CTGAGACTTAGAGAA | 5521 |
rs114426493 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869382 | ATAAAAGCTGGAAAC[A/G]ATTTTCTATCCACAG | 5521 |
rs114428017 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642334 | TCATCAGTGTGGGAT[A/G]AGGGAATGGAGAGGG | 5521 |
rs114432261 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599629 | CCTCATTTCTCTTGA[A/C]ACCAGGCCTTTGAAC | 5521 |
rs114439857 | snp | A/C/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789252 | AATAGCCAAAAACTT[A/C/G]GGGGGCAAATGGGTA | 5521 |
rs114443054 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974154 | AAAGGTAAATAACAG[A/C]AATAATGCATATTTT | 5521 |
rs114444069 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689332 | CACATGCCACATGAT[A/G]TTTTGGTCAATAACA | 5521 |
rs114446612 | snp | A/G | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007922 | CATTCTTGAAGTCAG[A/G]GAGACCAAGAATCCA | 5521 |
rs114456526 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038807 | GGTAGAAAAATCCAG[A/G]ATTGAACCCAGGTGG | 5521 |
rs114459764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054163 | TTTTTTCTATATGAT[A/G]TAGAATGTTTCGTTT | 5521 |
rs114474955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703667 | TTTCCTTCTTCCTAG[A/G]CTCTGAAAATGTCTT | 5521 |
rs114505790 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733842 | GAAAGTACTGATTTT[A/G]TATTGAATTTGAGTC | 5521 |
rs114506469 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776509 | TTAACTCAAAATAAA[C/T]TACAAACTTCAATTT | 5521 |
rs114518860 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822705 | TCCTCCCACAGATTA[C/G/T]TATTAGAAAAGAGAG | 5521 |
rs114540231 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044131 | AGGGCCCTGCTTGAA[A/G]GAATTTGAAATCTTT | 5521 |
rs114542859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655525 | CAGTGAATTTTCATC[A/G]CTATCCTATGATTAA | 5521 |
rs114545856 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768973 | ACCTCTGCTTCTCAG[A/G]TTCAAGTGATTCTCC | 5521 |
rs114550814 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750201 | TTTCATACTATAGCC[A/G]TATAATAAATCTTAA | 5521 |
rs114555484 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708049 | GCAGCTTTAAAACTT[C/T]TTAAAAATTTAAAAT | 5521 |
rs114558005 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624587 | TACTCTTCCTCCTGA[G/T]GCTTCATTCTTAAAT | 5521 |
rs114558830 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651251 | ACCCAAGACTCTAAT[C/T]GTCCAAATTCAGCCA | 5521 |
rs114567069 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071147 | TTATGTGAGTATGAC[A/G]CCCAGAATTGTAGCA | 5521 |
rs114568497 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602741 | GATCAATCAGAATTG[A/T]AATTGCAAAAATTTT | 5521 |
rs114574522 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975173 | TCTCCATTGCACCGA[A/C]CCCCAGCCCCTGGTG | 5521 |
rs114600489 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741476 | GGAGTGGAGGGTGAA[A/G/T]CACTCCCGGTGTCCT | 5521 |
rs114604922 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819394 | GTAAATAGAACACTG[C/G]GGTGGGATGGGAGTA | 5521 |
rs114610528 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714344 | AGGTTTCAGAGAGAA[C/T]GGGAGGAGAGGAATT | 5521 |
rs114618606 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695895 | TAAAAAAGAAAATTA[C/T]ATAAGAACATGGGAA | 5521 |
rs114620810 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599076 | AAATAGGGTTAGTTT[A/G]TCTCCAGCACTTGAT | 5521 |
rs114636530 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856748 | CAAGGTAACACAATC[A/C]ACACTGTAAAAGCTT | 5521 |
rs114637548 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699345 | CTAGATGATGTCACA[C/T]GGGTTTGTTTCTCGG | 5521 |
rs114637824 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814521 | GATGGGAAAGTCTCC[A/C]AACAGACAGAAACAT | 5521 |
rs114640691 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760774 | CACCCTTGACTCGCA[G/T]AGTTGAAAAATTGCT | 5521 |
rs114646410 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706837 | TACCTTGACCTCAGC[A/G]ATGATGCTGTCCGTG | 5521 |
rs114659770 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751708 | ATCCTGCCTTGTGTG[A/T]TGAGTTCTATGAAGA | 5521 |
rs114659777 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631845 | CTTTAATAAAAGTTA[C/T]GCTCATTGTGTGCTT | 5521 |
rs114660896 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073013 | AATCACACTGGATTG[C/T]CATTAAAAACCATGT | 5521 |
rs114663846 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710675 | AAAGCAGAGGAGTAA[C/T]TAACTGCTCAGGCAA | 5521 |
rs114665632 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686315 | GCTAGACAGTGACAA[G/T]AGCTAAGCAAAAAAG | 5521 |
rs114666598 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597017 | TGTCACTCCACATGC[C/T]AGTGTTGGGTAGCTG | 5521 |
rs114677906 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854844 | CAGTGAAAAGCAGGT[A/G]TTTATCCTGGCTATT | 5521 |
rs114680615 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624839 | CTATTCCTCCTTATG[G/T]TACTGTACACAGCCC | 5521 |
rs114680935 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671313 | AGAATAGAAAAACAC[C/G]TCTCTGTCCTTAGGT | 5521 |
rs114685524 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733416 | CAGAACTACCCTTGG[C/T]CCATATTTTAAATAA | 5521 |
rs114685630 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633008 | GGCCAGTTTCTTCAC[C/T]CAGCCACCGATACTC | 5521 |
rs114691733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835499 | TTTGTCACCTGTCCA[C/T]ACTGAACTTGGGGCG | 5521 |
rs114701880 | snp | A/G | 0.0654984 | 0.168698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714017 | TCTTGGGGAGTGAGT[A/G]CATTAAAATAAATGA | 5521 |
rs114713732 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873469 | AGTCCAAACTCCTTG[G/T]GGTCAACAAGGCTTG | 5521 |
rs114715000 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681511 | ATGTCTTTCCCATTA[C/T]GCTTATAATTCAGAT | 5521 |
rs114735437 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656289 | GAGCCATGCAGCAAT[A/G]TGGGGAGGAGCATTC | 5521 |
rs114754693 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702907 | GGTTACTAAGTTCCA[A/G]ATGTAAGTTTAGAAG | 5521 |
rs114758275 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833606 | CTACTGTGGGAATGA[C/T]ATGTTGAAACAGTTT | 5521 |
rs114765631 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022398 | CCTGTCTCTGCTAAA[A/G]TAAAAAAAAAAAAAT | 5521 |
rs114767374 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961241 | AACAGCAACAAAAAC[A/G]CTTAGGAAGGGGGAA | 5521 |
rs114769349 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981203 | GAAGTAATGGATTCA[C/G]TTCTTCCCCTGCTTC | 5521 |
rs114786412 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838546 | ACTGCACTCCTGCCC[A/G]GAGGACAAAGTGAGC | 5521 |
rs114798516 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054762 | CACAACACCTCAGCA[C/T]CCTCAACCCTTTTCA | 5521 |
rs114799163 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989099 | GAGCAATGAGATAGG[C/T]ACAGTAATAAAAAGT | 5521 |
rs114800109 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047400 | ATCAAAACTTCACTA[C/T]ATACCCCATGAATAT | 5521 |
rs114803237 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744557 | GAAATTCCACTCCTA[C/T]CCTCACATGTGTCAC | 5521 |
rs114805253 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604438 | AAGGTTTCCAATTAG[C/G]TACCAGAAAATAGAG | 5521 |
rs114811004 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932256 | GTCCCTCAGCTTTCT[A/G]TCCTGGTTTGAAAGG | 5521 |
rs114821622 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950442 | TATGTCACATTTTTT[A/T]AAAAAAATTTAAGTT | 5521 |
rs114834128 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668925 | CTGTAGACTCCATTA[A/G]TTCATTTTCTTCCTG | 5521 |
rs114839745 | snp | A/C/G | 0.024468 | 0.107964 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929139 | GTGTCCCCACTGCCC[A/C/G]CCTACCTCTCTCTTC | 5521 |
rs114844101 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668864 | GCCATAGAATGGAAG[A/G]AAGCAGGGCACGGGT | 5521 |
rs114852226 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693835 | TGGGCAACTATTCTG[C/T]CATAATAACATGTTG | 5521 |
rs114855077 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010708 | ACCTACTGCCCTCCT[G/T]CTGTGTGGCCCAGTT | 5521 |
rs114859668 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071478 | GTCTGCCATCATCTG[A/T]CTCCATCTTTCACAA | 5521 |
rs114873113 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664499 | AAGACCCATCTTCAG[G/T]CTCCATTTTTAGTTC | 5521 |
rs114880252 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021377 | ATACTGGAGAGGTGA[A/G]AGTGGAGAAAGAGTT | 5521 |
rs114881776 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605904 | TGTGCCTTGTGTAGA[C/T]GTGTTTTCTGTTATA | 5521 |
rs114889851 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634183 | ATCTCATCAGTTGAA[A/G]GCCTGAAGAGAATAA | 5521 |
rs114891556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982237 | TTCATTTGTTGCCAG[A/G]TCCCACAATTTTTGA | 5521 |
rs114894009 | snp | C/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923453 | TATGGCAGTCCCAAA[C/G]CCTAATTATGAAAAC | 5521 |
rs114901037 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807658 | ACTTGCCCAAATTCC[A/C]AGCCAGAACGTGACA | 5521 |
rs114905314 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047458 | ATTTCTTAAACTCCA[A/C]CCCCCAAAATGTACA | 5521 |
rs114915592 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950982 | TGGTATACTATGATG[A/G]TATACAACCTCAGGT | 5521 |
rs114938265 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769513 | CTAGATTTGCAAGCA[C/G]TGTAAGGATCAGCAA | 5521 |
rs114940173 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689373 | AAGATTATAATACTG[A/T]ATTTGTACTGTGTCT | 5521 |
rs114953893 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631901 | GCCCTGTGTCCATGA[A/C]CTCTTTCCACTCTTA | 5521 |
rs114958557 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018470 | TCATTTTTTATATAT[A/G]TTTTTTAAAAACACT | 5521 |
rs114970301 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053433 | TTTGACTTTCACAGA[G/T]ATATTCACACACTAT | 5521 |
rs114998414 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985464 | TTTTGGGGTCAAATT[A/C]AAAAAATTATTGCCT | 5521 |
rs114999626 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983015 | ATTGGTGTATGTGGA[C/T]TATTTAGATTCAATT | 5521 |
rs115000703 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602840 | TCAGCTTTTGGGCTT[C/T]GGCTGAGTATTAGTG | 5521 |
rs115002645 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640718 | GAGGGGGAGGTGCTA[C/T]AGCTACAGTTATTTT | 5521 |
rs115018751 | snp | G/T | 0.0126979 | 0.078662 | intron-variant, utr-variant-5-prime, missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878608 | GGCCGGAATGAGGGT[G/T]CTGGTCCCACGGGAG | 5521 |
rs115022377 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916051 | ACTAAAAGCTCCTTG[A/G]AGACAATACATTAGT | 5521 |
rs115044665 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962012 | AAAAGCTTATTTAGC[C/T]AGTCTGGGATTAATT | 5521 |
rs115047016 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990505 | TGGTGGTGGAAAAAC[C/T]AGATAGTCACATGAA | 5521 |
rs115047517 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953574 | TCACAAAAAGATATA[A/G]AGTGATACAAAACTG | 5521 |
rs115051171 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604760 | ACCAGGAGGAAAGGT[G/T]CAGTAAGTCACCAGG | 5521 |
rs115068045 | snp | G/T | 0.0325976 | 0.123435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715749 | GAACCTGCCTTTTTG[G/T]GGGCTGCTTCTTTTC | 5521 |
rs115080540 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730123 | ACTCTTACATCAGTG[C/T]GACCTGGATATGAGA | 5521 |
rs115087584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802227 | ATTTCCCAAATTTGC[C/T]TTCCCTGCTCTCTCT | 5521 |
rs115091893 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971527 | CAAAGTTATTTCCAA[C/T]CTTTTTCTATGAGAA | 5521 |
rs115099612 | snp | A/G | 0.02016 | 0.0983543 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913241 | CTTGTTATTATTATT[A/G]CCTCTTCAGGATGGT | 5521 |
rs115102067 | snp | A/G | 0.0588605 | 0.161139 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617091 | TGGATGGAACTGCAG[A/G]TCTTTATGTTAAGTG | 5521 |
rs115109511 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642982 | GGATTGATTGAGCCT[C/G]GGAGGTTGAGGCTGC | 5521 |
rs115116082 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849652 | GTGCACTAACAAAGG[C/T]CTGATTTAAGTGCTT | 5521 |
rs115127454 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793487 | GTACTAATTCATTTA[A/G]GTCACTTATTTAATC | 5521 |
rs115143321 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723345 | CTTTCCTTTAAACTT[C/T]CATAGTGTCATTTTA | 5521 |
rs115148409 | snp | G/T | 0.029116 | 0.117091 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897008 | TCAATGATGAACTGA[G/T]CATATATTTGTCATC | 5521 |
rs115150472 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759225 | CATAAGGCTTAAGAA[C/T]CACCAGACTAATAAT | 5521 |
rs115169556 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642377 | GGTAAGAGGTAGCAT[A/G]GGGGCCATTCAAACA | 5521 |
rs115190716 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758143 | TCTCAACATTAACAT[C/T]AGTGATGTCTGCTTT | 5521 |
rs115191036 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731789 | TAAGTTTTAGGAAAA[C/T]AACAATGTAACACAA | 5521 |
rs115203697 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595714 | GCAAACCAGAGGGAC[C/G]TTTTTCTACTAGAGG | 5521 |
rs115216303 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903171 | TTTTCATAAAAGCAT[A/G]CCATTGATGTTAATA | 5521 |
rs115228419 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886765 | TGTTCATGTTTTCGT[C/T]AAAATATTTTAGAAC | 5521 |
rs115230853 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830296 | TAATTTAAGCCACAC[A/G]TTTAACACAGTATCT | 5521 |
rs115235682 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838740 | AATGATTAATAGGTA[C/T]GAATTTGTCCATCAA | 5521 |
rs115244043 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684993 | ATGTTTCAGCCACTT[A/G]TAACTTGTCTCCTCC | 5521 |
rs115244804 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811249 | GTGATCTGTCCACCT[C/T]GGCCTCTGAAAGTGC | 5521 |
rs115245584 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707212 | ATGTTGTCCATGTTG[C/T]TCCCAGCCGTCTTCT | 5521 |
rs115257721 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699994 | GATGCCTGATTTAAT[A/G]CTGAACACTTGAATT | 5521 |
rs115265844 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636667 | GGACTGGATACTATG[G/T]GAACCAGACTCTGGG | 5521 |
rs115273344 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970234 | GCCCAGATTTGAAAC[C/T]AGTGAGTCTGGCACC | 5521 |
rs115273518 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917075 | TACAAATAATCCCTA[A/T]ATTATAGGAATTATT | 5521 |
rs115284198 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655752 | ATCTTTCAGCGAGGG[C/T]GATCACGCTGCCATG | 5521 |
rs115293701 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978502 | GCTTTTATGATTTTA[C/T]GTACTACGTTTAAGT | 5521 |
rs115301801 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928748 | AGATCATTTTGAAAA[A/G]TGAAGCTGATCATAT | 5521 |
rs115309034 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728501 | TGGGACTGCTGCACT[C/T]CACATCCTGTTGGTT | 5521 |
rs115323330 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781706 | TAGCCCACCACCACA[G/T]TTCACAGAATCATAG | 5521 |
rs115324839 | snp | A/G | 0.096524 | 0.197345 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840083 | AGAGCTAAAATGAAA[A/G]GTTAATTATGTTGAT | 5521 |
rs115326728 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595875 | GCATGGGATTTTGGA[C/T]GCCAGACTGAGTGTC | 5521 |
rs115332690 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651931 | TTTAACTCACCTATG[C/T]GGGAGTTTTTAAATC | 5521 |
rs115333475 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821010 | GCCTTCTAATAGGCC[G/T]CCCTCCTTCCATCAT | 5521 |
rs115347528 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885036 | AACCCAAATGCCCAA[C/T]AAAATAATTTGTTAG | 5521 |
rs115353154 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948771 | AAATTAAGATAATAT[C/G]CTTACTTTCAAGAGG | 5521 |
rs115353523 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843675 | AATGGTTCTACTTGC[G/T]TCTTCTATCTTACAG | 5521 |
rs115361778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651333 | TTTGTCTTAGAGTGC[A/G]AACCAGGTAGTGTCC | 5521 |
rs115373873 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642394 | GGGCCATTCAAACAT[A/C]ATTTCCTAATCCCAA | 5521 |
rs115374341 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813888 | CAAGCAGGAGGAGTC[A/C]TGGCAAGATGGCAAC | 5521 |
rs115381146 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635475 | GTTCATCAAGCTTCC[C/T]AGTCAGTTGATTCCC | 5521 |
rs115381412 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687583 | ACTAGGTGAGAAAAC[A/G]CTTGTAATAGAAATG | 5521 |
rs115395243 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940512 | AACATTTGCTAGGGG[A/G]AAAAAAAAAAAACAT | 5521 |
rs115397459 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687384 | GGGTATTCTACTTAA[C/G]TGCTTGGAGCCTCAT | 5521 |
rs115406188 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893139 | TGATGTGTTTCTCTT[C/T]ACTGAAGACCCAGCT | 5521 |
rs115412028 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966228 | ATTGTTTATTATTGA[A/G]CACTGCCACCTAGTG | 5521 |
rs115414177 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592833 | TTCAAGGGTCACTAG[C/G]GGCCCACATTATGCA | 5521 |
rs115414934 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853148 | TTGCTTCAAAAAAAT[A/G]TCCCCTAGGAAATGC | 5521 |
rs115430417 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798038 | ATAACTACTCCATCC[C/G]AGACAGGCATTTGTC | 5521 |
rs115460114 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958157 | ACATTAATCGCAGAT[C/T]TCCCGAAGGCCCCAC | 5521 |
rs115461814 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626657 | TGTTACAGGGCATGA[C/T]GACAGGTAAGTTGGC | 5521 |
rs115465058 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948429 | TCCTTGATACTGTTC[C/T]TGGAAGATGGTAAAA | 5521 |
rs115478574 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783528 | CTTATGCTTTTTCCA[C/T]TTTCCAAAGTCCATA | 5521 |
rs115484411 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018401 | GGGATAGTTGGACTC[A/G]ATTTGGAAGGGTCAA | 5521 |
rs115486589 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980203 | TGTGTGCATGTATCT[A/T]TGTTTCAGAGTAGAC | 5521 |
rs115491072 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657885 | AATTGAGATTACATT[G/T]AGACTGACAGTATAT | 5521 |
rs115512214 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624320 | CCCTGCAAACTGTTG[C/T]TGTGAACTCGCTCTA | 5521 |
rs115518106 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762591 | CTACATACTCTTTGG[A/G]AACAGATTTCTGGTC | 5521 |
rs115519560 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843698 | TCTTACAGAGTTATC[A/C]TGACCCTGAGATAAT | 5521 |
rs115522706 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677807 | TGCTGGGATTACAGG[C/T]GTGTACCACCACTCC | 5521 |
rs115523827 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827004 | ATAAATATTTGAACT[A/G]AAGTTAGCACTTACA | 5521 |
rs115523837 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693969 | CTTTTGCCCCTTGCT[C/T]CATTCCTCCACTTCT | 5521 |
rs115525692 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796945 | AGAATCAGCTTGATT[C/T]CACCAGCCTGTAACT | 5521 |
rs115535332 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735895 | AAGTATTTATTGAAT[A/G]CCAAATATGTGGTGG | 5521 |
rs115556671 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797359 | GGTATTTACATAGCA[C/T]ATTTGATTATGCAGT | 5521 |
rs115559622 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993695 | TGGCTATAGTAACTA[C/T]CTTAAAGGACTGCCT | 5521 |
rs115563785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762960 | GAGTTCTCTAGTTGA[A/G]CCTCTGTCATTTGGC | 5521 |
rs115563981 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831958 | TGATAATCCTGACCC[C/T]GTGTAGGCCTAAGGT | 5521 |
rs115566780 | snp | C/T | 0.030278 | 0.119257 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965711 | TTATAAGTACAAATA[C/T]AATGCCCTAATATCA | 5521 |
rs115585412 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001570 | AACACTCACTGTGAG[G/T]CTCTGAGGCTTCATT | 5521 |
rs115587308 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980885 | TATCCTTACTAGTTT[C/T]CTGTGTTGTAACCTA | 5521 |
rs115592615 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805426 | ATCCTGCCTGGTCTA[C/G]CTCTTTGTTGTCTAA | 5521 |
rs115594546 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921552 | ATTTCGTTTCTTAGA[C/G]AGACATGAGAAAAGA | 5521 |
rs115623246 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593696 | TGGGGTGAGGGGAAG[G/T]CTCTCCAAGCATAGG | 5521 |
rs115627608 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994753 | GCATGTGAATGGTGA[A/G]GAGTGAGGCTCTGCA | 5521 |
rs115630294 | snp | C/T | 0.00290393 | 0.0379939 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055779 | ATCTAAATAAAAAAA[C/T]AGTCTCCTGAATCCA | 5521 |
rs115647120 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753623 | GAATGTAAGGAATTC[A/G]GTCTGATGCTCGGTT | 5521 |
rs115674616 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606214 | GATTAGGTAACCACA[A/G]GTGCAGGCTGTTGCT | 5521 |
rs115678117 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616783 | GTGGGAATGAAAATT[C/T]GAAAAACCACTATGA | 5521 |
rs115680212 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639871 | TAAAAATTGACATGT[A/G]ATAACTGCAAATGCG | 5521 |
rs115687796 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809814 | GAATGGATTGGAGGT[C/T]ACATGGAGCAGAGAG | 5521 |
rs115699657 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786231 | ATATGTAGAATACTA[C/T]TGAGAAGGACTCATT | 5521 |
rs115703077 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922879 | TGGCTCAGAGAACTA[C/T]GAGGGAAGAGGTTCT | 5521 |
rs115707705 | snp | A/G | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867800 | GAGAACAAGACTATA[A/G]GCTTATACTTCACCA | 5521 |
rs115708676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907048 | AGGCAAGAGGCTCCT[C/T]GGCTGATTGTGGTGA | 5521 |
rs115727135 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833002 | AAGCCCTTTGCAAAC[C/T]AGATAGGGAAGGTAT | 5521 |
rs115727165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060401 | GGAGGCTGCAGTGGG[C/T]AGATCACTTGAACTC | 5521 |
rs115729780 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778531 | ACTTCTTGATTTTTT[C/T]ATCCTAGGGACTGTG | 5521 |
rs115733354 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050163 | ATTGTACATAAAATT[A/C]AAAAAATATGTTTCA | 5521 |
rs115733659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732015 | ACTTTTTCCCGTTTA[C/T]GGTTTAAAAACAACC | 5521 |
rs115755727 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833564 | AACTTCAGGGCATTC[C/T]GTGGTTATGAAATCT | 5521 |
rs115765010 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690878 | CTAAGATTATAGTAA[C/T]GTCTGGCAGTGGCCA | 5521 |
rs115767072 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024040 | TTCTTGGCCTTTGGG[C/T]CCAGACTGAGTTACA | 5521 |
rs115775462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883096 | TGACCTAAGCCAGTC[C/T]GGAGATTCTTAATAG | 5521 |
rs115781532 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599790 | TCTCCTAATGCTAGT[C/T]CTCCCTGAGCCCCCC | 5521 |
rs115794361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764460 | TTGCCTCTTCTGGAT[A/G]GCTCAAGTCAGTAAT | 5521 |
rs115796895 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892404 | CCTTCCCTAGCTTCT[A/G]CAGGCTACAAATAGC | 5521 |
rs115806064 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794498 | ACTTACAATAAACTG[C/T]CACAGCAGAGCTATA | 5521 |
rs115806378 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015612 | CTCTCATAACACAAC[A/C]CAGTATTGCAGAGAG | 5521 |
rs115811227 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067805 | TCATTAACATCATGT[A/G]GGTAAATAATACTTG | 5521 |
rs115835764 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657976 | TTATAACCACACACT[A/G]GCCCCAGATAAGGCC | 5521 |
rs115851630 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023278 | CCAAAACAAAGAGGT[A/G]TAGCAAGGAATTCAG | 5521 |
rs115875332 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737096 | AAGTCTTCAAATCCT[C/G]GTGTGTATTTCATAC | 5521 |
rs115890108 | snp | A/C | 0.00915317 | 0.0671402 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782060 | GTGTAGCACCTCCCC[A/C]ACCCATGCTCCAGCG | 5521 |
rs115894007 | snp | C/T | 0.096524 | 0.197345 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691907 | TTTACTTTCCTCTTG[C/T]GCTTGCATCCCAACC | 5521 |
rs115896992 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806872 | GTATAAAAGTGCCCC[C/T]GACAGGGGAGCAGGC | 5521 |
rs115902820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690762 | GATTATTAAGTTTGT[A/G]TTCTGAATCACAAGA | 5521 |
rs115904355 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681234 | AAATTAGTTCTTTGC[A/T]TAACCTAGTAGCAAA | 5521 |
rs115905669 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625345 | AATGTATTCTTAATG[A/C]TAGAAATGAGCAAAC | 5521 |
rs115916693 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848064 | AGCTGTCCATACTCC[A/G]TCATTTTACCTGCGT | 5521 |
rs115931104 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068919 | TAATTTTGGGAAAGG[C/T]TGCTTTAAATCGTAA | 5521 |
rs115938429 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665943 | GATTTGCTTGTTGCA[A/G]TGTTGCTACAAACCT | 5521 |
rs115941157 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839540 | ATAGTAAAATGTATA[C/T]GCAATTTCCAAAAAA | 5521 |
rs115949419 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758334 | AAACAGCTTTGTGAT[A/C]TGGGGCAAGAACCCT | 5521 |
rs115954584 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712790 | AGGAGGACTGGTCTT[C/T]GGTCAAGGGTATATG | 5521 |
rs115956433 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988856 | CAGACAAAACGAATA[A/G]TCCTTTAGTTAGGCT | 5521 |
rs115957995 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007144 | CTGGACTGACCCGCT[G/T]GTCCTTTCACTGACC | 5521 |
rs115960436 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797813 | GGCTCAGGACTCCAA[A/C/T]GCACAACTGCAATTT | 5521 |
rs115966486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786174 | AATTACTATATATCA[A/G]TAAAACTATAATAAA | 5521 |
rs115975686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659928 | ATGAGGTTTTAGCAT[C/T]TCTTCCATCCACCAA | 5521 |
rs115983376 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722043 | ATTATTACTACCCCC[A/T]TTTTACAGATGAGGA | 5521 |
rs115986832 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728854 | GCCATGTGGAACCAT[A/G]TAAGTCCAATTAAAC | 5521 |
rs115987987 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980262 | CATATACTGAAGATA[A/T]GGTAACAGAAGGAAA | 5521 |
rs116006288 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785309 | CCAAGCACTCTAGGA[A/G]GCCGAGGCAGGCAGA | 5521 |
rs116006835 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707497 | TCAGGAGAAGCTCAA[A/G]GAGCTGATGCAGACA | 5521 |
rs116010640 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744700 | CCTCCTCATTCCTCA[C/T]ATCTGAGAAACAAAG | 5521 |
rs116022861 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928953 | TTCCGGAAAACATGA[C/T]ACTGGCTTTTTGGAG | 5521 |
rs116039532 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027615 | CCCTCCAGCCTGGCA[A/C]CAAAGCGAGACTCGG | 5521 |
rs116054898 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785038 | AATCGTAGCACTCCA[G/T]TTTACTTAGCAATAA | 5521 |
rs116057818 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777895 | TTTAAAAAGATGAAT[A/G]CACTGTTACGAGGGA | 5521 |
rs116062496 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734107 | TTGCTGAGGCTGGAG[C/G]GCAGTGGCATGATCA | 5521 |
rs116063219 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589331 | GCTTACAAAAAAAGA[A/G]CATAGCAGGGTTGAT | 5521 |
rs116063463 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624353 | GCACCTTCATCTAGG[G/T]GTGTGCTCAGGCCAA | 5521 |
rs116082062 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630568 | CTAGTTGCCTCATCT[C/G]TAAGATGTGAATAAT | 5521 |
rs116083419 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849115 | TGCTACTAGTAGCAT[C/T]AGACATTTCTTCAAG | 5521 |
rs116097127 | snp | A/G | 0.0248432 | 0.108648 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589417 | GGCTTAAATGAAATT[A/G]TTCAAAGGAAAATGG | 5521 |
rs116098478 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783932 | TCAAGGAAGATCAGA[A/G]TATGTATATATCTTT | 5521 |
rs116101999 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987375 | CCACCCATATCTTTA[A/G]TGTAAGTACCAAAAG | 5521 |
rs116109390 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888966 | CCTATATTGCAACTA[A/G]ACTGTATATATTTAT | 5521 |
rs116114902 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708564 | TTCCTTCATACTGCT[C/G]TTTTTAGTGGACAAT | 5521 |
rs116117175 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967523 | ATTCTAAACCAGAGC[G/T]CTGGTTTGAACCTAG | 5521 |
rs116117731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677073 | CTTTGTCTGCTTTGA[C/T]GATCTTATGTTTCCC | 5521 |
rs116121065 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596895 | AGCCCTGCTGGAACA[C/T]AGAGTCATCAAAGTC | 5521 |
rs116121729 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057267 | AGTTCTGCAATAATC[A/T]TATTACCTCCTTAGA | 5521 |
rs116123228 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080350 | TTTCAGGCAAGCCCT[A/C]CTGCATTCTGCTAGA | 5521 |
rs116124001 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753590 | AGATTCTTGCCAGCC[A/G]AGGACACTTGGCAGC | 5521 |
rs116126872 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668029 | CCTTTTCCTAGGATA[G/T]TCCTTTGTTCACCTC | 5521 |
rs116139214 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051036 | CTCTGCACTAAACCG[A/G]GATGCCAAGACTGAA | 5521 |
rs116146276 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843324 | ACTATACAAGGTGAA[A/G]TACATAAATCCAGAC | 5521 |
rs116147254 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801939 | GCTGGAATGAAAGGG[A/C]GGAGCAGCTGCATGT | 5521 |
rs116147993 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793456 | AAGGGAGAATTGTAC[A/C]TAACAGTGGATCCAA | 5521 |
rs116152411 | snp | G/T | 0.0232847 | 0.105357 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766287 | TCCAGTATTTTTAGG[G/T]TTAAAAAAGATGTCT | 5521 |
rs116152718 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840270 | ACTCCTCTGTGCCAG[A/G]CACGTTGTCCTTACA | 5521 |
rs116154001 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602947 | AACAGCTATGTCATT[A/G]GTATTGGAGGTTTGG | 5521 |
rs116173340 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076429 | GCATAATCAAGAGGT[C/T]AGAAAAATATAAACT | 5521 |
rs116183401 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676191 | CTATCTAGGCGGCTT[C/T]TCCATGTTGGTGAAC | 5521 |
rs116183442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621121 | CCTGGAGGGACCCTG[A/G]TGTGAGCTGGTCACT | 5521 |
rs116207647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709937 | TTTGCACAGGGCCAG[A/G]TTATTAATGCATGTT | 5521 |
rs116216006 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591338 | CCAGGTAAATTAAGC[A/T]AAGGTTAGATTTTGT | 5521 |
rs116218785 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893012 | TTCACAAACCCTATG[C/T]GCAGAAACAGTGGGC | 5521 |
rs116219599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887816 | CCAATGAAGGTGGAG[A/G]AATTTAAAGGTACAG | 5521 |
rs116222083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637203 | ATTGTAACAAATACA[C/T]TGTAGATACAAGAAT | 5521 |
rs116236091 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603643 | TTTAATAGCAGCTCC[A/G]GGAATTATTTTCCTT | 5521 |
rs116238146 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744214 | CACACCATCCCCTGC[A/C]CCCACCCTTTTAAAT | 5521 |
rs116239157 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642560 | AATTTCCAAGTCTGT[A/G]AAAACCATAGTGCAC | 5521 |
rs116239745 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670993 | CAGAGTGTAAGGTCA[G/T]TTCTCAGTTTAAAAA | 5521 |
rs116240059 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072728 | CTCTACCCTGACCAG[A/G]TATTGTGCAGCACTT | 5521 |
rs116240566 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886022 | TCAGGATTTCTTTTG[C/T]GGGTGTTGAAAATGT | 5521 |
rs116245042 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958151 | GAGCAGACATTAATC[A/G]CAGATCTCCCGAAGG | 5521 |
rs116257118 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719065 | CTATTTACTGAGCAC[C/T]TTCTATGTGCCTGAC | 5521 |
rs116257544 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948092 | CTGTGTTCATATAAT[C/T]GTTTCCCTTACCCTA | 5521 |
rs116258112 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897787 | CGGATGCTATACAAA[A/G]AAGGAAAACATAGAG | 5521 |
rs116261019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053723 | TATCTAAGAAAACAC[A/G]TGGGGCATGGGACTC | 5521 |
rs116269702 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726895 | CAGTTCTGTGGCTAT[A/G]TAAATGTTAGATTTG | 5521 |
rs116291858 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836157 | AGAGTAATTCTGCCT[A/G]CTATGCCCTCCCCAT | 5521 |
rs116293398 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830044 | ATATTCTATGCAAAA[C/T]ATATAGTACAATGGC | 5521 |
rs116298560 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629331 | CAAGCACCAAACCTA[C/T]GAGTTATCTTAGATT | 5521 |
rs116300832 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954186 | CTCTCTCCCTCCTCC[A/G]AACCTCACTCCTGGA | 5521 |
rs116315103 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849355 | TAACTTTAATTCATT[A/C]CCACATGTAGCATTC | 5521 |
rs116320427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754267 | ACATGTGCTGAGGAG[C/T]AAGCAAGTACCCCCA | 5521 |
rs116322281 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700743 | TGACAGATCCCATTG[A/C]AAAAGGAGGAGTTAC | 5521 |
rs116342977 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055200 | GTGAACCAATCCAAC[A/C]ATCAACACTCCACAG | 5521 |
rs116347918 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864986 | TCTAGAAACATAATT[G/T]TTCATACCATTTAAC | 5521 |
rs116352927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920334 | GCTGTGTGCTATAAA[A/G]CCCTTACCAGGCCCA | 5521 |
rs116354658 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049774 | AGGCCTGCAAAGGCA[A/T]GACTGGACTCTGCAA | 5521 |
rs116363433 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921423 | TCTCTCATGTGAGGT[A/G]GGACAGAGCAGTGGA | 5521 |
rs116380826 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896211 | CCTGTTTACCTCATA[A/G]TCAAATCATCCACAA | 5521 |
rs116383608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664701 | ATGAATGGTGAGTGC[A/G]TCCCAGAAGATGTTC | 5521 |
rs116389414 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668112 | AGTTAACAGAGCTCA[C/T]CTCATTCCTCCTTTC | 5521 |
rs116390193 | snp | A/T | 0.077417 | 0.180873 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624426 | CTACATCTTTTTTTT[A/T]AAAAAACAGTTCTAT | 5521 |
rs116403349 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673892 | TCTTATCTGCACTTG[C/G]AGTTTCCCATTCTCA | 5521 |
rs116403959 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646000 | TTCCTCTTTCAGATC[G/T]TAACTAATTCTTCAG | 5521 |
rs116404953 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811047 | GCCCTGTCGCCACCC[A/G]GGCTGGAGTGCAATG | 5521 |
rs116408260 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616744 | ATGAGGATGTGGAGA[A/G]AAGGGAACACTTGTA | 5521 |
rs116410555 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691622 | TCATAACTCTGGAAG[C/T]AGGTGCTATTATCTC | 5521 |
rs116412161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686128 | GGCTACTCTAAAACA[C/T]GGTTTCCATTTCTGT | 5521 |
rs116416803 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639076 | GTGGAAACGGATGCT[C/T]CATGTGCATAAAGAA | 5521 |
rs116429672 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795808 | CAATTACATCTCAAA[A/G]CTGAAAAAGTCAATT | 5521 |
rs116434449 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591991 | AAGGCTAAGATAGAG[A/G]AAAAACTTGAGCAAT | 5521 |
rs116445571 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811878 | AGCCAGAATCAACTA[G/T]GTATTATCTGTCACT | 5521 |
rs116461745 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834794 | CTTCCCCTTCAAGCA[A/G]TCCTCAGTGTCTATT | 5521 |
rs116463004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892336 | GAAATGTAAAATAGC[A/G]TTGAAATAATAATTC | 5521 |
rs116464811 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040468 | GTACAGAAAGCTTAG[C/T]CCAGGTCAGTTAGAC | 5521 |
rs116465156 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665708 | CCTGTGTTGGCTTTC[A/G]ACATGTCTTCCTCAC | 5521 |
rs116473993 | snp | A/G | 0.0654984 | 0.168698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946737 | ACATAAATAAAACAT[A/G]GCTTCACTACTGTAA | 5521 |
rs116487480 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714429 | GATGGTAAGGAAAGT[A/G]GGATCAAGAGAGTAC | 5521 |
rs116495899 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027048 | ATATCTATCATCAAG[C/T]AAAAGAATAAAAAAA | 5521 |
rs116519070 | snp | G/T | 0.0498117 | 0.149749 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593183 | GCTCTTTGAATCAGA[G/T]GGCCTTGGATCTGAA | 5521 |
rs116528133 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849639 | ACAGTACAAGAGGGT[A/G]CACTAACAAAGGTCT | 5521 |
rs116528714 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589118 | GTTGAAGAGAAAAAA[G/T]CCAAGGAACATGTAA | 5521 |
rs116529183 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638632 | AGGCAGCATTAGAAC[A/T]CAGGTCTCTTGACTC | 5521 |
rs116530605 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631131 | TGCTGGGCTCCTCAC[C/T]GCCTTGCCTCATCCC | 5521 |
rs116533611 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985901 | ACAAAAATTGGTATC[A/G]TTTCTATACAAAAAC | 5521 |
rs116553875 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966721 | CCTGGCACAGCGTAG[A/G]AGCACAAAAATATGT | 5521 |
rs116570448 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007141 | CCCCTGGACTGACCC[A/G/T]CTGGTCCTTTCACTG | 5521 |
rs116571697 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941391 | AAATTATGACAAACC[A/G]GCCTGAAATTCTTTA | 5521 |
rs116574675 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923561 | CCCTAGTGGGTTTGT[C/T]GGAAGCCCTTCTTGG | 5521 |
rs116583997 | snp | A/C | 0.030278 | 0.119257 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862871 | TTGGAAAAAAAAAAA[A/C]AAAAAACCCTGGCTT | 5521 |
rs116585821 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966495 | AGCAGAGCCAAAGAT[C/T]GGCCTCCTCTGACAT | 5521 |
rs116587208 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975323 | CATCCATGTTATAGC[A/T]TGAGTAAGAATTTCC | 5521 |
rs116597208 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727849 | TTCCCATACCCAATT[A/G]CTCCCCCTTCCCCTA | 5521 |
rs116601897 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656797 | ACCACCTTCACTGTG[C/T]GGGTGAGGAAAGCTC | 5521 |
rs116610673 | snp | C/G | 0.0168055 | 0.0901129 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591457 | TTGCCTCCATGATCT[C/G]GTTTCAACTTCTATT | 5521 |
rs116619119 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709566 | TGGGAAAGAGTTTTC[A/T]TCCCTGAATAAAAGG | 5521 |
rs116622436 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870071 | CCCTCTACACCCTTG[C/T]GTGTCTGTAGAGGGA | 5521 |
rs116624106 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990230 | TAAATAGAAAAACAA[A/T]CTTAAAATTCATGTG | 5521 |
rs116625316 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937470 | ATGTGTTATTAAGGG[G/T]TTACTTAAATACTAA | 5521 |
rs116627009 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929767 | CTGGAGATAGACTAC[C/T]AGGGTTTATATCTTG | 5521 |
rs116628333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981454 | TGTTTTCGAGAATTC[A/G]GTTGTGAGTCTGATA | 5521 |
rs116630650 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833696 | CATTGGAGTGTCAGG[C/T]GGGCCGTGTCTCTTC | 5521 |
rs116634912 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798913 | TCTGTCTTCTTTTTC[C/T]TTGTGAGCCTGTTTA | 5521 |
rs116639821 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636216 | ACTAGAAACTGTGCT[A/T]CTCCAACCGGGGTAC | 5521 |
rs116642920 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690253 | CATGTTCATAACTGA[A/G]CTCATCATCCAGTCC | 5521 |
rs116652717 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817890 | CAGTTCATGACTCTG[A/G]CTCCCATAAAACACC | 5521 |
rs116662244 | snp | C/G | 0.169061 | 0.236535 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861377 | CCTATATTTTTAGTA[C/G]AGGTGGGGTTTCACC | 5521 |
rs116663330 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871526 | TATATAACAGAAGAA[A/T]TCTACAGGAGTAAGT | 5521 |
rs116674554 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836460 | TGTCCCAAATTGCAA[C/T]GAACTGGACTCCACT | 5521 |
rs116679836 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997765 | TAAAGTAGATATTTC[C/T]ACAAAACCTAGCAAC | 5521 |
rs116693733 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629732 | TTCTCCCTCCCTCTC[C/T]TCCTCCCTTCCTCCC | 5521 |
rs116695989 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004964 | GCTATACAAGGAAAG[A/G]ATCTTACTGTCTGGA | 5521 |
rs116709098 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751268 | GCAGAGCTCTACTTC[C/T]GGGCATCACAGAACA | 5521 |
rs116720678 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742218 | ATATTGCTCCAAAGG[G/T]TATTTCTTTTTTTGT | 5521 |
rs116721515 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828637 | AGATAATACCAGAGA[A/G]TGACTGTATGGACAA | 5521 |
rs116722330 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891373 | CAATAAATGTTTGCT[C/G]TTGGTATTAGGTGTT | 5521 |
rs116724959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618442 | CAGAACTGTAAGGAC[A/G]TTAATCAATTTGTGT | 5521 |
rs116726451 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603272 | GAGTACAGAACCTGC[A/G]GACTATTTGAAAGAC | 5521 |
rs116727786 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606925 | GGCTCGGAATCATGC[A/G]CAGGGCTTTAAATTG | 5521 |
rs116741862 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057815 | ACATTGACTTGCTGT[A/G]TGATCTTGGGCAACT | 5521 |
rs116742982 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064784 | CACTGATACCAGCAC[A/T]TTGAAAAATAGCAGC | 5521 |
rs116747859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774211 | AATACCTAACTCATG[A/G]GGTTAAGAGTTGAGT | 5521 |
rs116754852 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974061 | CTAGAGAGTAAAGAA[A/C]TAAGTAGATTAAGTT | 5521 |
rs116757556 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709066 | CGTTCTGTTTGATCC[A/G]GAATTGTTTCCTCTG | 5521 |
rs116758637 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855365 | CACCTGCATGGAGTC[C/T]CTATAAATGCATAAT | 5521 |
rs116764544 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789297 | AAAAAGATGTTGGGT[A/G]TGTGACATAACCCTT | 5521 |
rs116765984 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782250 | TTTATTTATAGCAAT[A/G]CAGGAACGATCTATT | 5521 |
rs116772430 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006165 | ATTAAGGGAAAAAGA[C/T]GCAATGGGTACTCAA | 5521 |
rs116777398 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631226 | TGGAGGTAAGGCACC[C/T]GGTGGGGCTCTTCAG | 5521 |
rs116782721 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596065 | TCTGTGGGCCGTATG[A/G]TCTCTGTGACAGCTA | 5521 |
rs116808027 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753400 | GCAGGACCTCAATAA[A/G]TTTGTATTGAATAAA | 5521 |
rs116809672 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734533 | AATTCACTTCCAGGA[C/T]TGTTTGATTTCAAAG | 5521 |
rs116824713 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024579 | CTGGGCTACAAAGTG[A/G]GGCTCAGAGAATTTA | 5521 |
rs116828245 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966414 | TGTAGACTCCCCTCT[A/G]TCTTCGCGCAGTTGT | 5521 |
rs116835365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705372 | AAATGATCATAGTTA[A/C]CAGGTTTGTGTTGAG | 5521 |
rs116840514 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627904 | CTTCTCATTGGAACT[C/T]GGGCTGTTTCTCCAA | 5521 |
rs116881943 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742863 | AGGGAGAATAGCACA[C/T]GAAGGCGATGAAGGC | 5521 |
rs116897646 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888608 | AAGGCTTTTATTGGC[C/T]TCCTACACATTCAGA | 5521 |
rs116943431 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068667 | CTGATGAGAAGCTGC[A/G]CTTTACATGAATCAT | 5521 |
rs116952840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599345 | ATCCTTCCATCTGCA[C/T]GCTACCATCACCAGA | 5521 |
rs116956011 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673777 | TAGCTCAGTGAGAAC[C/T]TGAAAGTTTACTGAG | 5521 |
rs116958790 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814162 | AAACACTCCCTCCCC[A/T]AATAAATACTGAAGG | 5521 |
rs116967443 | snp | C/T | 0.00355106 | 0.0419871 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040707 | TCCGTGTGAGGAAGG[C/T]AGCACTTACGAGAAC | 5521 |
rs116994921 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665316 | GCTAGATCTTCTGGA[G/T]AGCTTTCTGCAGCTT | 5521 |
rs117002561 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767414 | GCAGCTGGTTCTTCC[A/G]TGGTATAGAGTGAAT | 5521 |
rs117015008 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696245 | AGTAGCCAGGACTAC[A/G]GGTGCCGGCCACCAC | 5521 |
rs117027484 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709101 | CCAATCAGTGTCTAG[C/T]ATTTGGATACTGAAT | 5521 |
rs117031908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032613 | AACACAGATGTTTGG[C/T]GTTCCATTCTTGAGT | 5521 |
rs117089620 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995619 | TTCAACTCCATATTT[C/T]CTGCATTGCTACTAC | 5521 |
rs117120504 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047264 | ACTATAGTTAACAAT[A/G]ATGTCTTAGTTACAA | 5521 |
rs117151469 | snp | C/T | 0.081446 | 0.184634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036247 | TTGAGCTCCCACTTA[C/T]AAGACATAACATGCA | 5521 |
rs117170550 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723575 | ATTGTGAGTAATTAA[C/T]ACCTCAGAATAAACA | 5521 |
rs117226427 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872159 | GGATCATTGGTACAT[C/T]TCTGACCAGCACTCA | 5521 |
rs117242503 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064950 | TTTTTCTTGCTGATT[A/G]GAAAGCTAGTATTCT | 5521 |
rs117304004 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634694 | TCTTCAGCTTGCTGG[C/T]TGCAGAGCTTGGGAC | 5521 |
rs117317236 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987716 | AGAGGAATAAAGGAA[C/T]AGAGGAGTTATAAAA | 5521 |
rs117331126 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834467 | GTTTTGGTTTAGCTA[C/T]AAATATTTCACTTGT | 5521 |
rs117334103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875752 | CCCACCCAGTAAGAG[A/G]GTATAAGTTAATAAG | 5521 |
rs117335763 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708062 | TTTTTAAAAATTTAA[A/G]ATTTATATATAGGCT | 5521 |
rs117379088 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641102 | TTGCTAATGCTGATC[A/G]GGGGCCAGGCCTGCC | 5521 |
rs117381018 | snp | A/C/T | 0.011919 | 0.0763696 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686209 | GATTGTTCCAGGTGC[A/C/T]GGAGTTGCAGGAGAG | 5521 |
rs117386490 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675938 | TGCCCCAGGACTAAT[C/T]GGAAGCTTATCTTTT | 5521 |
rs117397882 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802531 | GGAGCATAATGAGTT[A/C]TGTGAAAATGAACTT | 5521 |
rs117407890 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697006 | CCAGTCTTTAAAAAT[A/T]TTCATGTATGTTTGA | 5521 |
rs117415186 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642265 | GAAGACACCAGGAGG[A/T]CACTCCTTAAGGGAT | 5521 |
rs117428274 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629737 | CCTCCCTCTCTTCCT[C/T]CCTTCCTCCCTCCCT | 5521 |
rs117440549 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854889 | CTTAAAATTTGGACT[C/T]TGAACTGTCTCTCGC | 5521 |
rs117471635 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653342 | TATAATGGTAGTGGT[A/G]TTCATAGTAGTGTGG | 5521 |
rs117474617 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794172 | GATATCTGTACATGG[C/T]TAATGACTACAGCTT | 5521 |
rs117510817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730992 | GGAAAGGGTTAGAGA[A/G]GAAGATTCAGCCATG | 5521 |
rs117551764 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723013 | GATCCTCAGATTGTC[A/G]TCTCTTCCTCCAGGA | 5521 |
rs117613396 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864720 | CCTCTCAGAAAGGGT[C/T]GAAGTACCTGGAGCT | 5521 |
rs117616369 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983020 | TGTATGTGGACTATT[C/T]AGATTCAATTACATT | 5521 |
rs117641752 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699650 | CTTTATCATCACTGC[A/G]AACTTAATTGGTTTT | 5521 |
rs117655436 | snp | C/G | 0.040671 | 0.13668 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951513 | TCTCCCCCATCTCCC[C/G]ACAGGTCCCTCCCAA | 5521 |
rs117674640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042881 | GAAGAGCATTCCAGA[C/T]GGAGGGAGCCACAAG | 5521 |
rs117692287 | snp | A/T | 0.04875 | 0.148319 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034863 | CTTTCTCAAGTGAAC[A/T]TTAGGAACCAGGTAA | 5521 |
rs117702583 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595744 | GAAAGAATAAAGTGA[G/T]ATGTATACATGAGCA | 5521 |
rs117748543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802751 | CATGGTGGGGATGGG[A/G]TAAGTATATAGTGAG | 5521 |
rs117765084 | snp | A/C | 0.0352966 | 0.128072 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923877 | CATATACACCGTGGA[A/C]TACTATGCAGCCACA | 5521 |
rs117766077 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996743 | GAGAAACAAGTGAAA[A/G]GCAATCCTGAGGTTT | 5521 |
rs117782949 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969240 | AGACCTGAAGGAAAA[C/T]AGATATTAACTATAT | 5521 |
rs117794797 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788795 | ATCCTTTGGGTTACA[C/T]TTAAACACTCTGCAA | 5521 |
rs117813294 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642999 | GAGGTTGAGGCTGCA[A/G]TGAGTGGTAATTGTG | 5521 |
rs117819828 | snp | A/G | 0.0832709 | 0.186283 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002726 | CTTCTGATCACCAGG[A/G]TCCAGGGACCATTGC | 5521 |
rs117829374 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820802 | TTTAAGTTCCTAGGA[C/T]TCCATCCGTCAAATT | 5521 |
rs117857090 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823670 | ATCTTGGAAATGGAT[C/T]CAATCATCCATGACA | 5521 |
rs117858179 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669091 | GAACAAATGTGCAGT[C/T]CATTTAAAATCACTG | 5521 |
rs117871412 | snp | G/T | 0.231111 | 0.249285 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926171 | TTTTTCTTTTCTTGA[G/T]TATGGGTAACACTTT | 5521 |
rs117880177 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966532 | AGGCCCCTCCCTCAA[C/T]ACTCTAATCCATCAT | 5521 |
rs117908345 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593809 | GATGATCAGTTTACA[C/T]AGGCCCTTTATTCTG | 5521 |
rs117933751 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044779 | TGTTTCTATAGGAAT[A/G]TATGCAGCAGAGCAT | 5521 |
rs117940356 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925522 | ATTGCATGGATGCTC[A/G]CCTTTCTATGGTGCG | 5521 |
rs117950227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063912 | TTTAACGTCTTTTCA[A/G]GAAAACACTTTTAAC | 5521 |
rs117959071 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685884 | GCAGCCCTCACCCCC[A/C/T]GCCTTCCACCCCACC | 5521 |
rs117980625 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814286 | GCCATCTTCTTCAAA[C/T]GCTGCTTTCTTCCCT | 5521 |
rs118017261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737946 | CCCTGTCTCAAAAAA[C/T]AAAACAAAACAAAAA | 5521 |
rs118024961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711144 | TGCCTGTTTCAGTCT[C/T]TTCATTGTAAACTTC | 5521 |
rs118033853 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785676 | AATAACTAGCAAAAA[C/T]CAGAATGGAGTAATT | 5521 |
rs118039951 | snp | C/T | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920267 | CATCATAGTTGCTCC[C/T]GTAATAACTAGTGAC | 5521 |
rs118040960 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991139 | GAATGTAAATTAGTA[C/T]AGCCATTATGGAAAG | 5521 |
rs118095882 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068566 | TCATGAATTTGGTTT[A/C]AACTGCTATTAAATA | 5521 |
rs118098866 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892736 | CAGTTTGAAAAAAAG[C/T]GTCATGCTATAGCCC | 5521 |
rs118109024 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818614 | TCTATCCCCTTGCAT[C/T]TTAAGTTATGTAATT | 5521 |
rs118137052 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914270 | GACCTTCTATTATGA[A/G]CAAGATGAAATGCAA | 5521 |
rs118147970 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052736 | AGAATATGCAGGCCC[C/T]GCTTGCCATGGAAAC | 5521 |
rs118154998 | snp | A/C/T | 0.0174303 | 0.0918166 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931172 | GTGATATCTCTGTAA[A/C/T]GCAAGCCAGAACCTT | 5521 |
rs118179421 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691683 | GTCCTTACCATGTCC[C/T]AAAAGGCCCTTCATG | 5521 |
rs118181203 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750051 | AGGCTGTCTTTCCTC[C/T]GTTGAATTGCTTTTG | 5521 |
rs137858291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904499 | AAAGTTGTAGAAAAT[G/T]CCACAGGCAGTATTG | 5521 |
rs137861554 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977206 | TTATCCTTGGATTAT[C/T]GTAATAGCCTTTACT | 5521 |
rs137864799 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928516 | TCTCTCATACCATCA[G/T]GAAATTCTGCTGGTT | 5521 |
rs137871002 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645914 | AACATGTCATACTCT[C/G]TCCTGCCACAGGACC | 5521 |
rs137889057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618180 | GGCTCAGTGTAATGA[C/T]CATGGTCCTTATAAG | 5521 |
rs137904118 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691379 | ACATAAACGTTTGGC[C/G]TGCATAAATCCCATG | 5521 |
rs137906525 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051628 | TTAGGAAAAGAAAGC[A/G]TCCCTACTGATTTCT | 5521 |
rs137908158 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643839 | TATATAAATGGATAG[-/A]AAAAAGTGTGAGTCC | 5521 |
rs137915980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648873 | GTGAATTAGGGAAGC[A/G]TGACAAGACTGGATA | 5521 |
rs137919188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041856 | CCTTGTTTTTACTAA[C/T]GCTATTTTTAGACTC | 5521 |
rs137924879 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019338 | AATAGAAAAGATTCA[G/T]AATAAATTGTTACTT | 5521 |
rs137927582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901187 | ACAGATAGTTAACTT[A/G]TTGGTGCTAACATAA | 5521 |
rs137931028 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971812 | TTAACATACTTTTTT[A/T]ATTTTGGAATAATTC | 5521 |
rs137942278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738878 | TAACTATTAGTCATT[A/T]GTTGGTGTGACTAGA | 5521 |
rs137943377 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768935 | TGCCTCTCACTGAGG[C/T]TGAGGCTGAATTGCT | 5521 |
rs137947794 | in-del | -/G | 0.0718919 | 0.175435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632605 | CCAGTCAGCAAGACA[-/G]AGGCTAAGTAAAGCA | 5521 |
rs137948560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694465 | CATTTGCAAAGTTAA[C/G]ATCGTATATTTTTCT | 5521 |
rs137949819 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962217 | ACTTGTTTTTTTCTT[A/T]GGGTCAGTTCAAATT | 5521 |
rs137954112 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657952 | AATTAGGAAGTGCAC[A/G]TAGGAAGGTTATAAC | 5521 |
rs137960232 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682617 | CACTCCACAGGCTGC[C/T]GTCTGGGCATAGTGA | 5521 |
rs137971721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924310 | TACAAGGACAACTGC[A/G]ACTGAAAAGCACAAA | 5521 |
rs137984593 | in-del | -/T | 0.204611 | 0.251898 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848139 | TTTCTTATTCTTTAG[-/T]TTTTTTTTATCTTAT | 5521 |
rs137987635 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797821 | ACTCCAACGCACAAC[G/T]GCAATTTTCCTTTTG | 5521 |
rs137991723 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726475 | ATTAACAATAGTGAC[C/G/T]ATATTTATTGAACAA | 5521 |
rs137993378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825268 | AAGCAGCTGTTTCTC[C/G]TCTTTGGTTCAGCAG | 5521 |
rs137995008 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871468 | CCAGCTAGTTCTCAC[A/T]TCTTGATTGCTCAAT | 5521 |
rs138010893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757323 | AGTGAAAACTTTATA[C/T]AATGGTATCACATAT | 5521 |
rs138029951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046239 | AGGCAGTTGACAGAA[G/T]ACTGAATTTGCTCCC | 5521 |
rs138031452 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000324 | CACTGAACTAAATGA[A/C]CCTCTAAGGGCTCTT | 5521 |
rs138033649 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083216 | CCTGGCACAGTTCCT[A/G]TATCAATAGTTATGA | 5521 |
rs138038321 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964065 | TTAAGTCAGCTGGAC[A/T]CTGGGGTTCAAAGAT | 5521 |
rs138058490 | snp | A/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865947 | CAGCCACTCACTTAG[A/C]CGATTAATACTGTTT | 5521 |
rs138065023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675862 | CTTGCACAGAAAATT[A/G]AGGTAATGATTTATA | 5521 |
rs138079686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847644 | ACTAAGCACTCTCCA[C/T]AATTCTGCCACTGAA | 5521 |
rs138085061 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751746 | AACAGAGTTAAGTCA[C/T]AGGGAATAATGGTGA | 5521 |
rs138086453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827709 | TATTGATAAAGTATC[A/G]ACTCCATGCACAGCA | 5521 |
rs138089969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860073 | AGTGATTTTACCTTT[A/G]TCTTGGACTATGGTT | 5521 |
rs138092514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640309 | TATTACTTGGGTCTC[C/T]GGGGCATGTGAGTCT | 5521 |
rs138115142 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890340 | TAGAGGTCAGGTTGG[A/C]AGCCTTTATGCTCAG | 5521 |
rs138119886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820810 | CCTAGGACTCCATCC[A/G]TCAAATTGCCAACCT | 5521 |
rs138126036 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673725 | AACTGCAGCTTCTTC[C/T]CTAGAAAGGAGTGAC | 5521 |
rs138132462 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817789 | CTCTCATCTAGGCTC[A/T]GTTTCATTTCTTTGA | 5521 |
rs138143523 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713955 | TGATATAAATTTGGG[A/C]GTTATTAGCATTCAG | 5521 |
rs138145150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760546 | TAAGACTGTATGTGA[C/T]GAATTATCAAACTAA | 5521 |
rs138170016 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927370 | ACTTAAGTCCAACAC[A/T]TGCTAGTGGCTCTAG | 5521 |
rs138170209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725162 | CATGCCTGGAGCCTG[C/G]AGAGCACACAATTTC | 5521 |
rs138174610 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591477 | CAACTTCTATTATCC[C/T]CTAAAAGGGTTTTAC | 5521 |
rs138183539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709114 | AGTATTTGGATACTG[A/G]ATATTCTTCCTTTCA | 5521 |
rs138192991 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625651 | TCTTCCTGGAGGAAT[A/C/G]TGCCTTAACTGAAAC | 5521 |
rs138198289 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881103 | TGGGAGTAGGCTGCA[G/T]AGATCAGTCTTCAAA | 5521 |
rs138212267 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069259 | GTATGAAGAGCTCTA[C/T]GTCAGAAGCGAAAAC | 5521 |
rs138217057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719003 | CAACAACCACACCTG[C/T]AGCACAGAATCCCAA | 5521 |
rs138223984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820578 | TACTGCAATATTATA[C/T]ATAAAAAACGCCATG | 5521 |
rs138225537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037063 | AGTAACTTTGCCCAC[A/G]TTAGCATACAGTAGA | 5521 |
rs138230342 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590395 | TTTTTGTTTTTTTTT[G/T]GTGTTTTTTTTTTTT | 5521 |
rs138232913 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990429 | ATCCATGCACTTTTA[A/C]CCAACTGTTTTTTGC | 5521 |
rs138252023 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839087 | TAGAAGCTTGTTCTA[A/G]TTGTGCCTTCCTAAA | 5521 |
rs138252490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748765 | CGTACCACAGTTTGA[C/T]GTGCTGTTCACACAT | 5521 |
rs138252900 | in-del | -/ATTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670503 | TTATTTATTTATTTA[-/ATTT]TTTATTTATTGAGAC | 5521 |
rs138256631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671536 | ATCATGACACAGTAG[C/T]GCCTAATACTTACTG | 5521 |
rs138257589 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912753 | ACCTTGTGATCCGCT[C/G]GCTTCGGCCTCCCAA | 5521 |
rs138257624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958028 | AGGGAAGTAGGAAAA[C/T]CTGAGTTGGAGGAGG | 5521 |
rs138283720 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036591 | TTGAGGAATTGCCAC[A/G]CTGTCTTCCACAATG | 5521 |
rs138288843 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770894 | TTAGTTTACAGAGAA[C/T]AACCTATTTACTTTC | 5521 |
rs138295211 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666350 | CTGAGATATGGAACC[A/G]TAAATATAGTATTAT | 5521 |
rs138301755 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032353 | CGCAATGTGATACCA[A/C]CTTACTCCTGTAAGA | 5521 |
rs138318279 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952894 | TTCAGACAAAATGTT[A/G]GCAAATGAATAGAAA | 5521 |
rs138335299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751332 | TCCAAGTGTTATGTC[A/G]CCTGTTGGGAATTGC | 5521 |
rs138348770 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990049 | AAATATCTCTACAAT[A/T]AAAACCATAAAACAT | 5521 |
rs138354085 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020068 | TGCTCTTTCTACCCA[A/G]TCTTTCTTCGTCCAC | 5521 |
rs138362529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871861 | TCCTTTGGTTCTCTG[C/T]ACCTTGAAATTTCTT | 5521 |
rs138365537 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800666 | GGTCACATAAAAAGT[C/G]ATAAGCCCATCTATC | 5521 |
rs138370809 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653535 | GAGCTCAAAGCAGGA[A/C]CCCAAGGGTCACAAA | 5521 |
rs138374262 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908374 | GTACTCAACAGGCAC[A/C]CATATTCTACTAGTA | 5521 |
rs138378823 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046325 | TTTCATACATATCTT[C/T]GAAGTCATACATTTC | 5521 |
rs138385741 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808285 | ACATTTCAAGGGCTC[A/T]ACAGTCACATGTGCC | 5521 |
rs138387576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849718 | CATCTAAGCCATGCA[A/G]AAAGGATTCAGGCTT | 5521 |
rs138389627 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739524 | GAGATTTCAATGAGA[C/T]GGAAGCATGGAGTGC | 5521 |
rs138391005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981095 | ATTGTATGTCTCCCA[C/G]TAGAATTTTAAGTCC | 5521 |
rs138400776 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847274 | AAGTTCAAATCTTCA[A/G]TTCAGCCTTTAATTC | 5521 |
rs138406500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981869 | TGAGACAATGAATAT[A/G]CAATAATAATAGAAC | 5521 |
rs138412400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697007 | CAGTCTTTAAAAATA[C/T]TCATGTATGTTTGAT | 5521 |
rs138417072 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023848 | CAGAAAAAAAAAAAG[G/T]AGAGGAAGGACAAAT | 5521 |
rs138432032 | in-del | -/AAAGGGAGTGACCGAGTATTACGGAG | 0.10606 | 0.204515 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590242 | TGCAAGGCAGAGAGC[-/AAAGGGAGTGACCGAGTATTACGGAG]AAAGGCAATGACATA | 5521 |
rs138439194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916957 | TTACTTATACAAATA[C/T]AAGTAATTACCAAAG | 5521 |
rs138462297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621690 | TTGAGCACCTACTAC[C/T]TGCTCCAGACATGCC | 5521 |
rs138466696 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761752 | TTCTGATCAATAAGA[C/T]GGAAAATAATAATTA | 5521 |
rs138470432 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875031 | TTAAAGGAAAATGAA[A/G]TAGTGCAGAATTTCC | 5521 |
rs138482038 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801254 | TGAAGATCTGATGTA[C/T]AGCAATGTGACTATA | 5521 |
rs138493564 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985996 | CCCTCTGACAAGTAT[C/T]CCCCAACAAGAACAT | 5521 |
rs138497843 | snp | A/C/T | 0.0322688 | 0.123198 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810969 | ATGAGTGAGAACATG[A/C/T]GGTGTTTGGTTTTTT | 5521 |
rs138498307 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911986 | CCCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 5521 |
rs138502622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743341 | TGGATTTATATATTC[C/T]CTTCATGTGTGACTT | 5521 |
rs138503030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872146 | ATTATTCACCCCAGG[A/G]TCATTGGTACATTTC | 5521 |
rs138514124 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704249 | TGTGTTTGCAGCATG[C/G]TCTTTGGTAAGGCAG | 5521 |
rs138517857 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602407 | CTGGGTGCTTAGCAT[A/G]TATAGTATTCAGCTG | 5521 |
rs138521282 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624349 | TATGGCACCTTCATC[C/T]AGGTGTGTGCTCAGG | 5521 |
rs138543031 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730223 | TAGGCTCAGTAACCC[C/T]TTTGTTTTGGCCAGT | 5521 |
rs138543840 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924828 | GTTTGCTGAGAATGA[C/T]GGTTTCCAGCTTCAT | 5521 |
rs138545728 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775072 | GAAGAATTAACACCA[A/G]TCCTTCTCAAACTCT | 5521 |
rs138549665 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649146 | AGATAGGGATATATG[C/T]GTTGATTTGACATAT | 5521 |
rs138559716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932549 | CTTCTCCTTTGCCTT[C/G]TGCCATGACTGTGAG | 5521 |
rs138560571 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698537 | TCCCACAGTGGCATT[C/T]GTAAATACTTACATC | 5521 |
rs138575003 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865539 | CGTATATATTCCCAA[A/T]AGAAGGCAAGTTCTG | 5521 |
rs138577271 | in-del | -/TCCCTCCC | 0.469937 | 0.118861 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677518 | TTTTTAAAAAACTCA[-/TCCCTCCC]TCCCTCCCTCCCTCC | 5521 |
rs138579090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648400 | CTATTCTATAAACGA[A/G]CCTTCAGAGCTTTAC | 5521 |
rs138582047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012946 | TGTGGTCTGAGAGAT[A/G]CCTGTTTGCAGACGA | 5521 |
rs138586742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041373 | AGTTCACCTGTAAGA[C/T]CCTTCCTTCAGCATT | 5521 |
rs138600569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897462 | TCTGCATTTTGGAAT[C/T]AGGGACTACAAAATA | 5521 |
rs138615396 | in-del | -/T | 0.0836354 | 0.186609 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987585 | TATTATAGCTATACA[-/T]TTTTTTAAGCCTCAT | 5521 |
rs138615451 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000830 | ATCATCTCCTGAGGG[A/T]TTTCCCTCCTGACTA | 5521 |
rs138617277 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713420 | TTTGATGCCACCAAA[C/T]TGTATACTGAAAAAT | 5521 |
rs138624446 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636757 | TCTTCAAGGATCAAC[C/T]TGATATGAACCATCA | 5521 |
rs138627190 | in-del | -/TGT | 0.0205511 | 0.0992634 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912995 | CTAACTTGCAGAAAA[-/TGT]TGTTAAAAACACTAT | 5521 |
rs138637476 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893765 | AATACCTAATGCATG[C/T]GGGGCTTAAAACTTA | 5521 |
rs138637686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961804 | ACACTGGTCCCCCAT[A/G]GAGGAGATTTTTTTT | 5521 |
rs138651444 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011118 | CTCCAACCACTTGGC[C/T]TCTTTACTGTATTTT | 5521 |
rs138652303 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825013 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCAAAAA | 5521 |
rs138655616 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756466 | TTCATTTTCCCCATG[C/G]TGCAGTGTGTATTCC | 5521 |
rs138663783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008766 | TATTCCCACACATCA[G/T]CTTTGATAAGTTCTT | 5521 |
rs138667991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996025 | TGACAATTTTTGTGA[A/G]TGGTTGGGCAGGAAT | 5521 |
rs138673166 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921913 | CTTGGATGAGTGCTT[C/T]AATTTATTTAACTTT | 5521 |
rs138674956 | in-del | -/C | 0.0770498 | 0.180522 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067413 | ATCATCTGGTATTTG[-/C]CTTTCTGTGCCTGTC | 5521 |
rs138674991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933681 | TTTTTTTTAAGTTTT[G/T]TTTTTCTTTTATTAT | 5521 |
rs138676965 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699835 | CTACCATCCAAATCA[A/G]ACTGTCAAGTGTGTG | 5521 |
rs138678054 | in-del | -/ACACAC | 0.311251 | 0.242381 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634764 | TAAATCTCTTAACTT[-/ACACAC]ACACACACACACACC | 5521 |
rs138690821 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003296 | TAAGCAAAGAAATTT[C/T]CAAAGGACCAAAAAA | 5521 |
rs138715822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793825 | CCCTGTCTCTAGGGT[C/T]ATACTGAGCTGCAAC | 5521 |
rs138717828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832975 | GCATGACTGTGTGTA[G/T]ATTAATATCACAAGC | 5521 |
rs138718253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077780 | TTAAAGTGCACTTTC[C/G]AAACAAAATAGGGAT | 5521 |
rs138720825 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719987 | CTCCTAACATTTCCT[A/C]GTGTACCCCCAGCCT | 5521 |
rs138724990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828486 | CTTTCTTTGTAATGA[G/T]TTTTTATGGTCTTAG | 5521 |
rs138749555 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633320 | CATCTCCAAAAGCCA[A/G]TGTTGCTTTTCATTT | 5521 |
rs138750868 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855257 | TAATTTTTCAATAGC[A/C]AGGGAAGAGCTGAAC | 5521 |
rs138757938 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790685 | AATATCCCTCCCAAG[A/G]ATAAATCCACCTGTG | 5521 |
rs138758730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748207 | TTAGCTAGTAAGTGG[C/T]GTAGCAGGAATTTAA | 5521 |
rs138763274 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900787 | ATGCCCCCCTCTCCC[C/T]GTGCCCCATCCCCAT | 5521 |
rs138764917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786774 | GTATGATGTAATCTA[A/G]CAAGTTCCTTTTTAT | 5521 |
rs138781149 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896942 | GGCTTAGCCTCTTAA[A/G]AAGGTAATGATCCTC | 5521 |
rs138782304 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963561 | GCATTTCTTTGGGGT[C/T]CCAAGTTTTTCCCCA | 5521 |
rs138783974 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850892 | TCTGAAAAATGACCA[C/T]GCAATCTATCCATAC | 5521 |
rs138786752 | snp | A/G | 0.0352966 | 0.128072 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912188 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 5521 |
rs138792517 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817063 | TGAGGGCTACTCCCC[A/T]CCCTGTATGCAGGCA | 5521 |
rs138802699 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073933 | CCCAGCTACTTAGGA[A/G]GCTGAGGCAGGAGAA | 5521 |
rs138807984 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598757 | ATCTGGCTACCTTCA[G/T]TGCTAATACACTCAT | 5521 |
rs138810596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597842 | ATCTATATAAGAAAA[C/T]TACTCTCCTTCCTTT | 5521 |
rs138832542 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710031 | TACTCTACCACACAA[C/G]CAATTTTCCTTCCCA | 5521 |
rs138842955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032179 | ATCCAGAATCTACAA[C/T]GAACTCAAACAAATC | 5521 |
rs138846303 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671243 | GGTGATTCATGTATG[C/T]TGATTTTAAGTATTT | 5521 |
rs138849592 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064703 | AAACAATATTTGTAA[A/G]TGTGTTTTGAAAACT | 5521 |
rs138851207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952725 | GGCAGTAACACCATC[C/T]GTATAGTCTGGAACC | 5521 |
rs138859234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797627 | CTACTGGGCATCTCC[A/G]ACTACCAGCAGCTAA | 5521 |
rs138878197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804395 | GCATCTGGCAGACCC[A/G]GGACTGGAACCCAAG | 5521 |
rs138878724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789937 | AGACAGAGAACATAA[C/G]TAGGTCTGCAAGGAT | 5521 |
rs138888219 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712139 | TAATAGTTCACAAGG[C/T]ATTATTATGTTACGA | 5521 |
rs138888236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666817 | CTTTCTGTTTCTGTA[C/T]GTTAAAACAGACTTC | 5521 |
rs138889578 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685957 | TGAGAGACATCAATC[A/T]ATAATAAAACATTCC | 5521 |
rs138891297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078254 | AGTATTGAGCACTGA[C/T]GCCAATGCTGTATCT | 5521 |
rs138897882 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982139 | GCTCTTCTTTTGCTG[G/T]GTTCTTCAGGTAGGA | 5521 |
rs138898917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601207 | TTTGAGTTGTTTCCA[C/T]TTTTTAGCTGCTAGG | 5521 |
rs138907222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736055 | GAGATAATTGAATCA[C/T]GGGAGCAGTTTCCCC | 5521 |
rs138917345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625066 | CTGGGACATGTGAAG[C/T]AACAATAAACATTCG | 5521 |
rs138926156 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943179 | TGTTTTTAGTACAGG[G/T]TATGGAATTGCAATC | 5521 |
rs138934551 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875292 | ACTTTAAAAGAGGAG[A/G]AAAGGTAGGGGAGGG | 5521 |
rs138936157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907550 | AAGTTGGAGAAAGGG[C/T]TAAGGGCAGGTGTAC | 5521 |
rs138951400 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682035 | AAGAAGCCATGGACA[A/C]CTTCCAAAGGGTTTG | 5521 |
rs138956510 | in-del | -/TCTA | 0.443195 | 0.158668 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024153 | TAATAAATCCCCTCC[-/TCTA]TCTATCTATCTATCT | 5521 |
rs138966454 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068720 | ATACATTCTGAACCA[C/T]GTGTGAATAATAAGC | 5521 |
rs138966591 | in-del | -/C | 0.0626037 | 0.165477 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034040 | TAAGGCCATATATGG[-/C]CTAGCGCCTACCTTC | 5521 |
rs138975210 | in-del | -/CT | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659504 | ATCAGTATTCCCCTC[-/CT]TAACGTTGGGGATAT | 5521 |
rs138975792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986116 | AACAAGAAGAGGCAC[A/G]TTGGAGAGGGGAGGA | 5521 |
rs138978587 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825597 | AAAGAAATACTTATG[A/G]ATGGATTGAAATAAC | 5521 |
rs138986426 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921534 | CTTTTACTGACACTT[A/C]AGATTTCGTTTCTTA | 5521 |
rs138990681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995476 | TTCTCTATGGCTGAA[C/T]GTGCAGGTTTGAATT | 5521 |
rs138990823 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881693 | CTGGGATTACTGGCG[G/T]GAGCCACCATGCCTG | 5521 |
rs138997651 | in-del | -/C | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988185 | TAGGAGAGTTCAACA[-/C]CCAACTTCAGCAATG | 5521 |
rs139005882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838902 | CAGCGTTAGAGGTTT[A/G]GCCCAGTCTTCCTCA | 5521 |
rs139018648 | snp | G/T | 0.003992 | 0.0444979 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835508 | TGTCCATACTGAACT[G/T]GGGGCGGAAAGATCA | 5521 |
rs139037725 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597145 | CAGCCATCAAAAGTT[C/G]TGAGTCCCTAATCCT | 5521 |
rs139039936 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880469 | CATTGCAGCTTCTCT[C/T]GGATATTGGCACAAT | 5521 |
rs139042099 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946139 | TTTAACGCTGTAGCC[A/G]CTTAAGCAACAGCTT | 5521 |
rs139053438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918605 | CTCTGAGATTCCACA[A/G]ACTTTTGCCTCTCTC | 5521 |
rs139059580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040364 | CATCTCAGCTCTAAT[A/T]TATCTGAATCAAAGT | 5521 |
rs139059666 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990980 | AAAAATCTTGAACAT[C/T]GTTAATCATCAAGAG | 5521 |
rs139073299 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598115 | TGTCCTCATAATGTT[C/T]CCATCTTCAGTTTCT | 5521 |
rs139074490 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992636 | GTGGAAACCCAGCAT[A/C]ATCCTCATGTGGTTT | 5521 |
rs139079322 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074501 | AACATCTAAGAAAGC[A/G]TATTTGTCAATCACT | 5521 |
rs139084239 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787848 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGTCC | 5521 |
rs139089955 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699238 | AGTGCTGAACCCTGG[A/G]TGTGTAATGTATTTG | 5521 |
rs139090446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711014 | CTGTGTGACTTCTTT[C/T]AAGCCCAACACAGCT | 5521 |
rs139096891 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956308 | AATCTCATGAATGGA[A/T]AAAACTTTGCCTGAA | 5521 |
rs139115213 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893950 | ACTCGGGAGGCTGAG[G/T]CATGAGAATTGCTTG | 5521 |
rs139116206 | in-del | -/AAA | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745389 | ATAAAAATGGGATCT[-/AAA]GAAGATCTGATTTGC | 5521 |
rs139117454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821465 | CTGGTTGTCACAGCA[A/C]TTTGTGGATGTATAT | 5521 |
rs139127086 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840273 | CCTCTGTGCCAGGCA[C/T]GTTGTCCTTACAGAG | 5521 |
rs139131555 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776093 | CACACAGATTCAATG[C/T]GATCCCTATCAAAAT | 5521 |
rs139136571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034961 | ATGGTGGTAGAAGGA[G/T]GGAGGTGTGGGGTGG | 5521 |
rs139149790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949143 | TTAGGAGTTTGCTAA[C/T]ATTTGACATGAGTGG | 5521 |
rs139174438 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809116 | ATCCAATGTCAGGGG[A/C]TTTGGGGGCAGCTTT | 5521 |
rs139176364 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851311 | GAGCATATTTACTAG[A/G]TTCCAGGCACTGTGT | 5521 |
rs139195679 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781986 | AATGGTTTAACACCA[C/T]TTCCCTTGGTACTGT | 5521 |
rs139221864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052025 | AGGGGAAGGAGTTAT[A/G]TGCTTCCTTAATGAG | 5521 |
rs139226903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873264 | ATCCATCTAATTCTC[C/T]CCATCTCTACTGATG | 5521 |
rs139227449 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919728 | CATCTCCATGGACAG[C/T]CCAAACAATAGCTCC | 5521 |
rs139237589 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777261 | ATAAATAAAATGTGG[C/T]GCATATGTAAATGAA | 5521 |
rs139241211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848535 | CTCCTCCAGTGGAAT[A/T]TATTTGATGTTTTTC | 5521 |
rs139245688 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048703 | CCAGTTGAGTAATGG[A/G]AGGTCATCCAGCAGG | 5521 |
rs139256538 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983455 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 5521 |
rs139264605 | in-del | -/GTCTT/TCTTG | 0.495634 | 0.0465208 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911086 | GTCTGTTAGACACTT[-/GTCTT/TCTTG]TCTTTTTTTTTTTTT | 5521 |
rs139266638 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909347 | CTTGGATTTTTATTC[C/T]AACCCCAATACACTT | 5521 |
rs139267119 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814245 | TTTTTCTCTTTTTTG[A/G]GGAGACAATGTTAGT | 5521 |
rs139271667 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700074 | ATAATGTGCAATTAC[C/T]AAATATATCACCTCT | 5521 |
rs139272243 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780275 | AGTCAATGAATTGAT[C/T]GTGGGATATTTTATA | 5521 |
rs139275263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745764 | GGAGATCAAGAGCAG[C/T]CTGGACAACATGGTG | 5521 |
rs139277487 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626284 | GTGGAGGGGAAAAAC[C/G]GGCTGTTGGAAGATC | 5521 |
rs139312332 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664889 | CTTCTCCATCAGAGC[A/T]CTTGGGTGACTAGGT | 5521 |
rs139317288 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654766 | TAAGCACCTTGTCCA[G/T]GGTCACCCTTCCGGG | 5521 |
rs139317767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922417 | TTGGACACATTTGAT[A/G]GCTTTTCATTTGTAT | 5521 |
rs139320326 | in-del | -/ACTT | 0.0640965 | 0.167152 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043958 | ATGTGACTTTGGGCA[-/ACTT]ACTTATCTTTCTGGG | 5521 |
rs139336561 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934971 | CAAAGCATTCATACT[C/G]CATCAGTTACCATTG | 5521 |
rs139337773 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866749 | ACATCCAGAATACTT[A/C]ACCTGATTCCTGCTA | 5521 |
rs139364230 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627055 | TTGAATGGGATAGAG[C/T]AGCTTCAGACATGGG | 5521 |
rs139369811 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978374 | AAGCTCTTTAGGTTA[A/G]TTAGATCCCATTTGT | 5521 |
rs139389638 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604341 | TCTGGTGCCTGAGTG[A/T]TAGAACTTAGGACAA | 5521 |
rs139390851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997013 | CTTTGACCTTCCATT[C/T]CCACCTTTTAAAATT | 5521 |
rs139408643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705606 | CCATATAAAACTGTG[A/G]TCTCCTTCTTGGGTC | 5521 |
rs139409485 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862045 | AAACACGAGTGAATG[A/G]AAGAATAAATAATCT | 5521 |
rs139418042 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731412 | ATGGAAAATTAAAAT[A/T]ATTTTGCAAGAGACC | 5521 |
rs139418390 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748982 | AATTGCCAAGTTGTT[G/T]TCCAGAATTTTTTCC | 5521 |
rs139420288 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700671 | AAACTATGTTTTTTT[A/C]CTCCTGCATATTCTG | 5521 |
rs139422809 | snp | A/G | 0.0248805 | 0.108725 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650662 | GTGATATGTGTGTGC[A/G]TTGGCAAATACTCTT | 5521 |
rs139422846 | in-del | -/TACGAAGGACTTGCAGTCA | 0.0236746 | 0.106192 | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081438 | GCGTCCTGGAGTGGT[-/TACGAAGGACTTGCAGTCA]TCCCCTGTGTGACTG | 5521 |
rs139426916 | in-del | -/AAT | 0.021354 | 0.101099 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592022 | AATAACAGATATGTA[-/AAT]AATAATATATGAATA | 5521 |
rs139427660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795172 | GTTAAGGAGATTAGA[C/T]AGGCTCCCACTTCTG | 5521 |
rs139429007 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923124 | TGAGAGTCTAAATTT[C/T]TTTTTTTGTTTAGCC | 5521 |
rs139432559 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623736 | GTATCATTATGAGCT[A/T]CGTGGGGATAGCATT | 5521 |
rs139435965 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826234 | GCCCAACATAATAAA[C/G]GGTGGCAGAGACAAA | 5521 |
rs139451726 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080227 | TGTTAGTTTGAGTAT[A/G]GTGTTCAATCCTGTC | 5521 |
rs139475418 | in-del | -/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768080 | TAACAATTGGTTTTC[-/T]TTTTTTTTTTTTGAA | 5521 |
rs139480180 | in-del | -/A | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987121 | TTCAAAATGATTTAG[-/A]AAAGCCCAACAACTG | 5521 |
rs139485879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672872 | TTCTAGATATATTTA[C/T]AGGCATGTACATTTT | 5521 |
rs139494210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641728 | ACAACTCTAAAGGGC[A/G]ATCCATGTTTTCAGC | 5521 |
rs139497495 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034602 | TAAAGTTTAAAATCC[A/G]TAATTTTTTCCCTAT | 5521 |
rs139508201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939495 | AGAGTCACACTGCTA[C/T]AAATTCACAACTTTT | 5521 |
rs139508919 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818257 | TGGCCATAGCACTTA[A/G]TACTGTGTCTGGCAC | 5521 |
rs139520374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935763 | GTAAAGTTTGGAAAA[A/G]GGTAGTAGAAAACAT | 5521 |
rs139523301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010529 | AGATCCTCATAAGGT[A/G]TGTGCAACCTAAATC | 5521 |
rs139527375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065645 | GCAATGGGGTTGGAG[C/T]GAGGTTGAGGGATTG | 5521 |
rs139532621 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022748 | CAGGAATACACATTA[A/G]GAATTACCATTGACG | 5521 |
rs139547520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806293 | TGCATCTCAGGCCTA[C/G]CAAGGAAATGTATTC | 5521 |
rs139558098 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623212 | TGAAAAATGCTACGC[A/G]TCAGAACTTTTGGGT | 5521 |
rs139571515 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752921 | GGGATCTGATCACTT[C/T]GGGGAACACAGGTGA | 5521 |
rs139586199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706558 | GCTGAAGGGCGGCCT[C/T]CAGCTCGGACAGCTT | 5521 |
rs139589702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629390 | AATCTCTCAGCAAGT[C/T]CTCTTAGCCTCACCT | 5521 |
rs139597252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796104 | TGCTGACTCAAACAA[A/T]GGTACACCAACAGAA | 5521 |
rs139606274 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026253 | TCAACAGATAAAGTA[C/T]GGTATATCCATACAA | 5521 |
rs139609271 | in-del | -/TAAG | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594872 | AAGGGCATTGGTGTT[-/TAAG]TAAGTTAAGAGTGAT | 5521 |
rs139612769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813323 | GGAGTTACATTATTT[G/T]GATGCATATTTTTGA | 5521 |
rs139640028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902287 | GCAAAATATTGTCAT[C/G]TCAGCATTGTTTTAT | 5521 |
rs139655628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910374 | TGAGACAAGGATGAG[A/G]CAAGTGTAGTGCCTC | 5521 |
rs139659479 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032575 | TTTGCATCCTCATAG[C/T]TTAGCTCTCACATAT | 5521 |
rs139660073 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798635 | AACAGTGCATTAACA[C/T]TGAGAACAAACAAAA | 5521 |
rs139671100 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836625 | GGTTCTGTGGCTTTG[C/T]CTAATGAATAACCTG | 5521 |
rs139671553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026994 | CTAAAACACAGTTCC[C/T]GGTAGCTTTTTTCAT | 5521 |
rs139703282 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944079 | CTTATCTCTTTAAAG[A/G]AGTAAATGAATACAA | 5521 |
rs139707475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637407 | TACAATGTATAGGAC[A/G]GCCCCTTCCCCGAAA | 5521 |
rs139711036 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660342 | TCCATTTTTTAAAAA[C/T]GTGAAAAGAAGCATT | 5521 |
rs139713441 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905846 | CAGTGGTGGTAGGTT[A/G]GGATTGATTTCAAAA | 5521 |
rs139732448 | snp | C/T | 0.00250347 | 0.0352912 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638204 | CTCTCCCCCAGCACA[C/T]TGGGGCCAGTGGCCA | 5521 |
rs139733715 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080444 | TCCAGTGTTTTGTAA[C/T]GCAGACACCCTTAGG | 5521 |
rs139733719 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687752 | CTATCTTCTATGAAA[G/T]ATATAGTCACATTCT | 5521 |
rs139752156 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806018 | AAGAAAAAGGCCAAC[C/T]CTTTCAGAATTTTCT | 5521 |
rs139767114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684621 | TCCTTGGGAGCATCA[A/G]ATGAGATGCCCAACA | 5521 |
rs139784864 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728694 | GGACTGGTCTTTCCC[A/G]TGCTATTCTCATGAT | 5521 |
rs139790033 | in-del | -/G | 0.0352966 | 0.128072 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924508 | GGACAGGACAACAGG[-/G]AGTCACCAAAGGGGG | 5521 |
rs139797419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913129 | GTTCTGAAGGCAAGA[A/T]TGAGTTTATATTCGG | 5521 |
rs139799575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986902 | ATATAAATAGGTAGG[A/G]GAAGCCCAAAGACCA | 5521 |
rs139800758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620314 | GGTCTGTTTGTCTTT[C/G]TTTTGTGAGGAATAA | 5521 |
rs139801346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873988 | TGGGCTTTTGTACCT[A/G]TTGTCCCTTCTACCT | 5521 |
rs139812356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996660 | AGGGCCTGGACTTCA[A/G]CAGTGGCAGGAGTAA | 5521 |
rs139819328 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993197 | ATCCACCTGCCTCAG[A/C]CTCCCAAAGTGCTGG | 5521 |
rs139824007 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799259 | CCTAATTTAAATTGT[C/T]AACACAGTACAAATT | 5521 |
rs139835040 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598586 | CCAAAACCAAACTTT[C/T]GATTTTCTCATCTAA | 5521 |
rs139837226 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802466 | AGTGCTCCTGAAGCA[C/T]CATCTCATTCCATCT | 5521 |
rs139842249 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901886 | GAAAATGCTTGGAGC[A/G]TTCAGGAACTGAAAC | 5521 |
rs139844362 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733191 | ATTCTTCCCTAAATA[A/T]GCAAGTAACCCACTC | 5521 |
rs139857852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609265 | GAATGGGGAAAAAAC[G/T]GAAAGCCTTTCCTTT | 5521 |
rs139858367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778144 | GCAATTTGGGTTCCG[G/T]CATTCCTGATAAAAA | 5521 |
rs139876069 | in-del | -/ATAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069780 | ACATGAACACATTTT[-/ATAC]TGTTTTTTTTTTTTT | 5521 |
rs139882640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887195 | TGACATATCTAAATT[A/C]TTTTCTTATATCAAA | 5521 |
rs139895692 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848006 | AAGTCACCATATCAG[A/G]ATTTAAAAGACAAGT | 5521 |
rs139903935 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782303 | AACCAGAACTCTCCT[A/G]TAGCTATTGAGGATC | 5521 |
rs139929738 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845008 | CATGAGATCCCACTT[C/T]TGGCCACTTCTTCAT | 5521 |
rs139929926 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958864 | CTCACAACAAACTTA[C/T]GCAATAGGTTCTATT | 5521 |
rs139948034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620637 | ACATTCCTACAGCCA[A/G]TGGGCTCCGGGAACC | 5521 |
rs139956221 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059150 | TATGAGATACCACCC[C/T]TGCTCTAAAGAAGTG | 5521 |
rs139971139 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744113 | ATATCTTTAAAGTAC[A/G/T]TAGATGCTTGCTCCT | 5521 |
rs139976556 | snp | A/G/T | 0.017061 | 0.0910646 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692830 | GGAGCCACCACACCC[A/G/T]GCCTAATTCAATTAT | 5521 |
rs139977013 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741119 | GGGATCTAGGCATCC[A/G]CAATTTGAAAAATTC | 5521 |
rs139978362 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753568 | ATTATTGATATTACA[A/G]GGAGGGAGATTCTTG | 5521 |
rs139981029 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661006 | AAAGAAATAGGGGCT[C/T]TAACTTAGACTGAGG | 5521 |
rs139985338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805115 | ATTTAATTGCAGAGA[A/G]TGATTAGCCAAATGC | 5521 |
rs139989522 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689738 | TTCCAGCCTCCAAAA[C/T]CCCTGCACATTCAGA | 5521 |
rs139990677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795412 | AACCTAATACATTAC[A/G]CCAAATGAAATGAAC | 5521 |
rs139991423 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736625 | CTGCCATCTTCTTCC[C/T]AGCCCCCAGCACCAC | 5521 |
rs140001744 | in-del | -/AG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049059 | GGTGAGAGGAGAGGC[-/AG]AGAGAGAGAGAAATC | 5521 |
rs140003237 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692695 | CCCACCACCACGCCC[A/G]GCTAATTTTTTTGTA | 5521 |
rs140015604 | in-del | -/AT | 0.380724 | 0.213099 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866629 | CACGCAGATACATAC[-/AT]ATATATATACACACA | 5521 |
rs140021674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959927 | GCAGGAGACAGATCA[C/T]ATTTCCCAAGCTAAG | 5521 |
rs140023309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979084 | CATTTCTACTTACTC[C/T]ACTTCAGTAACATTG | 5521 |
rs140030266 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974985 | TGAACCACCGTGCCC[C/T]GCCTATTTTTTAAAT | 5521 |
rs140040468 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895213 | TTCTTCTTCATTCAC[C/G]CACAGTTAATATCTC | 5521 |
rs140046347 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052854 | CATGGAGAACCAAAT[A/C]TCCTCTAATGTATGA | 5521 |
rs140058518 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779611 | ATTTCCTTAGAGGCC[A/G]ACAGTCTATTACAAC | 5521 |
rs140065244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826657 | TGCATTCTGGTGGCG[C/T]TTTCAAAACTCAGCA | 5521 |
rs140066137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872568 | TAAGTTTCCCCTTTC[C/T]TGAGCTTATTTGGAA | 5521 |
rs140067000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702488 | GGGCCACAAAGTAAC[A/G]TAGGTGAACTAGAAG | 5521 |
rs140072293 | in-del | -/TTTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906328 | TATTTATTTATTTAT[-/TTTA]TTATTTATTTGGAGA | 5521 |
rs140073688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940994 | AGGACATTTGTCCAC[C/T]GCTGGTGCATTTAGA | 5521 |
rs140074304 | in-del | -/GG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077705 | TCCATGCCAGTGGCT[-/GG]GTGTGTTTGTGACCA | 5521 |
rs140083090 | snp | C/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009210 | TTCTGTTCTGTTTTC[C/G/T]TCTTTACCCTGGCTT | 5521 |
rs140090438 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874541 | GCTTTCTCTGCATCA[A/G]ATAATTTTTCTTTGG | 5521 |
rs140092859 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004836 | TCCTTACTCAGACTC[A/G]TGGGACAACCCCACA | 5521 |
rs140097321 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935442 | ATTTTATTATAGCTG[A/C]CTGAATGGACTATGA | 5521 |
rs140099470 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867476 | TTGGTCCCAAATGCA[A/T]GGAGTAGAGAGGGAA | 5521 |
rs140100892 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985493 | CTAAACCAATGTCAT[A/G]TAGTTTTTCTCCTAT | 5521 |
rs140107034 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889442 | GTCAATCCATCATGT[A/C]TACATAATTGAGCTC | 5521 |
rs140113014 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830617 | GCAATCCCCGACTCC[C/T]GGGTTCAAACATTCT | 5521 |
rs140113868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762569 | TTAGTAGTTATTTCT[A/T]ACATATCTACATACT | 5521 |
rs140122351 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695196 | ATTAAGAAACAAACA[A/G]ATTTATTTGTATCTT | 5521 |
rs140128783 | snp | A/C/G | 0.0418435 | 0.138591 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619372 | GTAATCCCAGCTCCT[A/C/G]CAGAGGCTGAGGCAG | 5521 |
rs140137943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066845 | AGGGAAGCCAGGCTT[C/T]ATCAAGAGCCAAATA | 5521 |
rs140142391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939248 | TGGAATTTTCCCTTA[A/G]AAGTTGATACCTAAA | 5521 |
rs140143540 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944228 | ACTACATATATTCTT[-/T]GAGAAAAGGTATCCA | 5521 |
rs140158665 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646449 | GTCCTGATGTAGTTA[G/T]CCTATTAAGACGAAA | 5521 |
rs140158800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595470 | GTGCTTTGGAAGTCA[C/T]GCCCATTAGCAGGAA | 5521 |
rs140168436 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038897 | GTTTTCTAACTGCTA[A/C]GATACACTGCTTCTT | 5521 |
rs140170630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857655 | CAACTGTCTTCTAAC[A/G]GTAATATCTTAAGAC | 5521 |
rs140175663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791449 | TCTGTACAGCTTACA[A/G]GTCTGAGCTAATCGG | 5521 |
rs140178257 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727463 | ATCACTTTTTGTGGT[A/G]AGAATATTTTCAAAT | 5521 |
rs140187617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722229 | TATCTTACAGCTTTT[A/G]CAACATTAGATTTTA | 5521 |
rs140190435 | snp | A/C/T | 0.0197981 | 0.0977281 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642780 | AAAATCTTAGGGCCA[A/C/T]GCATGGTGGCTCGCA | 5521 |
rs140205206 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657547 | GAGCATCCACATTCT[C/T]CTTCCTAAAATCAGA | 5521 |
rs140208921 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803618 | TAGCAGGCCTAGCAA[A/G]TTAAATTTTTCAAAG | 5521 |
rs140215462 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734769 | AACCAAATCCTATAA[C/T]GTATAGAGAGGATTT | 5521 |
rs140229132 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915245 | AAAAATTTTTAAAAT[A/G]AATGTGAATCAGATC | 5521 |
rs140237712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853335 | TAGTATAGAGTTCCA[C/T]GTAGTTTAAAAAGTC | 5521 |
rs140238185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897916 | TAGGAAAGGCCAGGC[A/G]CAGTGGCTCACGCCT | 5521 |
rs140241582 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841909 | CACGTTCTGCACATG[C/T]ATCCCAGAATTTAAA | 5521 |
rs140259759 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774170 | TTTGTGTTTTAGTTT[C/T]CTGAAAATTGATAGG | 5521 |
rs140273606 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010797 | GACTCCTCTATGTGT[C/T]TCACACTTACTCCAT | 5521 |
rs140282523 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694222 | GACACACTGGCAAGG[C/G]TGCTAAGTGTATGAT | 5521 |
rs140290549 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738797 | GCTTATACTAGAGAA[A/C]AATAAAACTAATTAT | 5521 |
rs140308315 | snp | C/T | 0.000198069 | 0.00994963 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600310 | TAAGTCTCGATGGGG[C/T]GGTTTTCCATGTTGA | 5521 |
rs140309015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806887 | CGACAGGGGAGCAGG[C/T]AATAGGGGACCTTAG | 5521 |
rs140317070 | in-del | -/TTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976124 | TATTATTATTATTAT[-/TTG]TATTATTATTATTAT | 5521 |
rs140326139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711271 | TCATCAAGCAATCAA[C/T]CTTTTTTCTTTAATG | 5521 |
rs140326834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696530 | AAATCATCAGAAGTC[C/T]CTTTTATTCCAAGTA | 5521 |
rs140328132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964021 | ATACTTGACCTTCTC[C/T]AGGCATGTAGGCCAT | 5521 |
rs140340001 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897038 | CTCCTTTTCCCAAGA[A/T]CTCTTTAAAATGATA | 5521 |
rs140341468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059883 | CTAACTGCCTGTTTT[C/T]ACTGGTTCCAGTCCT | 5521 |
rs140350813 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672645 | GACAGCTAGAGAAAA[G/T]GGACACCATAGTTTG | 5521 |
rs140350844 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066516 | CCTGTGCTCTTCACT[A/G]TGGTGTCATGCAGCC | 5521 |
rs140354022 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000057 | CTGATTTAGACACCA[A/G]GGCTGTGATGATGGT | 5521 |
rs140358531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620807 | ACAGGTAGCTTTGTG[A/C]AGTTACTCCAAGAGA | 5521 |
rs140363054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007687 | AGGTCTGTGGCTTCA[C/T]TCCTGAAGTCAGCAA | 5521 |
rs140375369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968251 | CCAAATAAATAGGCA[A/G]TGATGGTGTTTAGGG | 5521 |
rs140384060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718788 | ATTTCAGTCACATAC[A/G]CAGTTTGAATTGGAT | 5521 |
rs140392507 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607429 | ACCAAGTTGCTTAAC[A/C]CTTGCAGTTTGCTTT | 5521 |
rs140396422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733510 | TGGCTTTCAGTAAGA[A/G]GTATGTGAACTAATA | 5521 |
rs140402021 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791406 | GCTGTGTGTATGTGT[A/G]TGTGGTGTGTGCACG | 5521 |
rs140402361 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046005 | GCCTCGTTAGATCTT[G/T]TCCTAATGTCATATC | 5521 |
rs140409828 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827592 | GGTAGATGTTAGGGA[C/T]AGAGAAGTGAACAAA | 5521 |
rs140411538 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900252 | ATAAGTGCCACAGTC[A/T]GAAAACATACCTGAG | 5521 |
rs140418189 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715943 | ACACACTCCATCAAA[A/G]TTTAACTCCTCAGAC | 5521 |
rs140457350 | snp | C/T | 0.000160489 | 0.0089565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877984 | CCCAACGGCGGAATG[C/T]GGCGGGGCTGGCGTT | 5521 |
rs140468830 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790112 | CTAGTTAATTGCCCT[A/T]CGGGACTGCTCTGTG | 5521 |
rs140470810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826884 | CATCTATTGCCCTGG[A/C]ATATCTGTTTTTTAC | 5521 |
rs140475398 | snp | A/C | 0.0337553 | 0.125452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036579 | GCTTCTAAGACTTTG[A/C]GGAATTGCCACACTG | 5521 |
rs140495319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944561 | TTTGATTGAAATTCA[A/G]TATATCTCCTGAGAA | 5521 |
rs140498151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643773 | AAAGAAAAAGGCATA[C/T]GGTATAATCCCAACT | 5521 |
rs140504746 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825595 | TTAAAGAAATACTTA[A/T]GGATGGATTGAAATA | 5521 |
rs140507975 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987572 | GTTTAAAATAGCTTA[A/T]TATAGCTATACATTT | 5521 |
rs140515936 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859143 | CTCCACCATAAACTA[C/G]GTATGTGATCATAGA | 5521 |
rs140516127 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926845 | ACTGCCCATATGCAC[A/G]GCCTCAGCCAGCAAT | 5521 |
rs140516256 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896318 | CTGAAGGAGGTATTA[A/T]TAACTATCATTGAGG | 5521 |
rs140536239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708760 | TCTTTCTGTCTAGAT[A/G]TTATTACTATTTGGG | 5521 |
rs140536860 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824891 | CCTGGCTAATTTTTT[G/T]TGTGTGTTTTTAGTA | 5521 |
rs140543957 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676980 | GAAGGAATAATGATA[A/C]CCAAGTGTGGCTTTG | 5521 |
rs140546296 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070241 | CTGTGTTTTCAACAC[C/T]TACTGCCCATATATA | 5521 |
rs140554265 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593266 | TCATGTAGATGATAT[A/G]GATTAATCAAGCTTG | 5521 |
rs140556908 | snp | C/T | 0.000955015 | 0.0218311 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146701063 | CTGCTCTCGTTGAAA[C/T]ATTACAACCCGACCC | 5521 |
rs140557082 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916689 | CAGATTCTTGCTATG[C/T]AGTTGAGTGTTTAAT | 5521 |
rs140561893 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820389 | AAACCATGCTAGGTA[A/T]AATGGAGCAGCCAGT | 5521 |
rs140564901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631933 | CTCCTGGAGGAAGGT[A/G]TCAACATCAGCACCT | 5521 |
rs140588248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839727 | ACATTACAAACAAGT[C/G]TGAAAACTGGAATGA | 5521 |
rs140592774 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816337 | CCCAGGAGGCTGAGG[C/T]GGCAGTGAGCCATGA | 5521 |
rs140603337 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674003 | AACTCTGACCATACG[A/T]CCAAGTTAGAAGTCT | 5521 |
rs140610565 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718481 | GTTCTTACACACACA[C/T]GTACATTTGGTTTTC | 5521 |
rs140621670 | in-del | -/A | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059320 | TTAGGCATTATTTAT[-/A]AAAAAATGAAAAGAA | 5521 |
rs140636247 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948159 | CTGTCTGTCTCTCCC[A/C]TGAGGCTTTAAGACT | 5521 |
rs140640188 | in-del | -/GCGC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018037 | GACACACACATGCAT[-/GCGC]GCGCACACACACACA | 5521 |
rs140653040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946314 | TTCCCCCTGTCCCCC[C/T]ACCACTGCTTGGAGT | 5521 |
rs140659444 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838502 | CTTGAACCTGGGAGG[C/T]GGAGATTGCACTGAG | 5521 |
rs140665745 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809846 | GGAAGCAGGGAGACC[C/T]GGTAGGGGCTCTGTC | 5521 |
rs140669568 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742786 | TAGGGTGGGTCCTAA[A/T]TCAATATGACTAGTG | 5521 |
rs140676860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808389 | GTTTTAGAGAATCCA[A/G]TTGCTGAAAATCATC | 5521 |
rs140677548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680916 | ACAGTCTCCTTTAAC[A/T]TGAAACCACCCTTGT | 5521 |
rs140685075 | snp | A/G | | | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767315 | CTGTAAGCAAATTTC[A/G]TTTAATTCATACTTT | 5521 |
rs140689648 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072317 | GTATCTGTAATGAAT[A/T]GTTTTGAATGAACAT | 5521 |
rs140706062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907299 | GATTATTACAACTAC[A/G]TATTTTAAGCCATCT | 5521 |
rs140718340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945798 | AAGGCAATTCGATTT[A/G]AGAAAGAATGTTACT | 5521 |
rs140733378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877088 | GCTAAGGATAAAAGG[C/T]CTACAGGTAGAAAAT | 5521 |
rs140738937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693371 | AGTCACATGCCACCA[C/T]GCCCAGAGAATTTTT | 5521 |
rs140743864 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023227 | TATGCTGCGACAAGT[A/G]TATTATAAATCCTAG | 5521 |
rs140754284 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883127 | AGGCTTTAGGTGTCA[A/G]ACAGTCCTGGTTTGT | 5521 |
rs140759927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769032 | GCAGGTATGTGCCAC[C/T]ATGCCTGGCTAATTT | 5521 |
rs140766810 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651101 | AAAGGGAGTTGTGGG[A/G]AAATTTTAGAAATGT | 5521 |
rs140779539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696891 | TTAATATGAGACTCA[C/T]TGTAAAACTTTACAA | 5521 |
rs140783847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620950 | ACTCCCAAGCTGCCC[C/T]GTTTCCAAGGCTGTC | 5521 |
rs140785388 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045053 | TGGATGTCAAGACAA[C/T]AAACAGGTGTCCATG | 5521 |
rs140798901 | snp | C/G/T | 0.00239393 | 0.0345281 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800258 | GACTTGTACTGATTA[C/G/T]CTATCTATGGATCAA | 5521 |
rs140819688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771220 | TCAGTGGCCAAGAAG[A/G]CTGAATGAGCAGTGA | 5521 |
rs140820304 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879922 | CTCAGTTAAGCTCCA[C/T]AAGTTTAGCTAGATG | 5521 |
rs140822349 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807559 | CTTTCATATAGACCT[A/C]ATTTCATACTTAAAA | 5521 |
rs140822957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903582 | TAAATATTTTTTGTT[C/G]AGATGGGGTTTCGCC | 5521 |
rs140830523 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695258 | GTTCTCTCTGGATGG[C/G]AACACTTTTATTATT | 5521 |
rs140851928 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017395 | CGTCTGTGCTTAGCA[C/T]CTTAACCTTAGGGGA | 5521 |
rs140857987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041028 | AGGTATTCCCAGGAA[C/T]GTCAGAAACAGTCAA | 5521 |
rs140867214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961057 | ATATTATTGTTATTA[C/T]CATTGTTGTTTAAAG | 5521 |
rs140869916 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756341 | CAATCCCAGCATCTG[A/C]AGAGATTACTCTGGT | 5521 |
rs140875221 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681542 | AATTTCATCTGAAAA[A/G]TTCAGAAAATAAAAG | 5521 |
rs140881297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648186 | TTAGGGCATGGCTCA[A/G]AGGAATCTCCCACTT | 5521 |
rs140894573 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653345 | AATGGTAGTGGTATT[C/T]ATAGTAGTGTGGTAG | 5521 |
rs140904194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797460 | CAACTTGCCTGCTTT[A/C]TTTTATTTTTAGCAG | 5521 |
rs140911536 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925809 | GTCCCACAGGTTTTT[C/G]AGGGCCTGTTAATTT | 5521 |
rs140916618 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001523 | TGAACGTCAGAGGAA[C/G]AAACTCTGGACACAC | 5521 |
rs140930758 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048253 | TGTTGTAGGCAGTCT[A/T]GTAGGGCAGCAAAGA | 5521 |
rs140947482 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792980 | ATGGCTACTGTGTGG[A/C]GAAGAGATTTGGGGG | 5521 |
rs140955575 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774569 | TGCCTATAATCCCAG[C/T]ACTTTGGGAGGCCAA | 5521 |
rs140955930 | in-del | -/TATT | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817441 | AAATAAATTTGCATA[-/TATT]TATAGTGTACAGTGT | 5521 |
rs140958636 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654272 | TTTTACAGGGGAGGT[A/G]GGGGGAGGTGGAGTA | 5521 |
rs140965077 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599814 | GCCCCCCACCCTCTG[A/G]CAGGCCCCGGTGTAT | 5521 |
rs140972470 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962982 | AGTGGAGCTGAATAG[A/G]GAACACAGGCCCCTT | 5521 |
rs140977760 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738123 | AGCTTCGGGCTGGGC[A/G]CGGTGGCTCACAACT | 5521 |
rs140980208 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789625 | AGTCACGGGCATGGT[A/C]CCTGCCCTCAAGGAG | 5521 |
rs140987832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685085 | CATGCTTAGTACAGT[A/G]TGTAGCATAGTAGAC | 5521 |
rs140987980 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927796 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTGACTG | 5521 |
rs140989094 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003977 | AGTGAGCCCTGGGCC[C/T]TGAACAAAATCTGGA | 5521 |
rs140993054 | in-del | -/A | 0.0376037 | 0.131863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726280 | TGGCCAATTTAAGCC[-/A]ACTAGGGAGTATTCA | 5521 |
rs141000656 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822221 | GCAGAGCCTTGCAAA[C/T]GAGGATGAACATTTG | 5521 |
rs141020149 | in-del | -/TCCAGTTG | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639273 | ATCAGAAACAAGCCA[-/TCCAGTTG]GAAAGTTTTAGGGTC | 5521 |
rs141026817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747758 | ATAAAATTATTTCTT[C/T]AATTTATGTTACTAT | 5521 |
rs141030236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670839 | TTTTAGTTAACTAAC[C/T]TTATTTTGATAGGGA | 5521 |
rs141041766 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607784 | AATAAGAAGCTGAGC[A/C]TTAAATGATCAAGAA | 5521 |
rs141041864 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656647 | TCCAGTGATCTTCCT[G/T]CCTCAGCCTCCTGAG | 5521 |
rs141048425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885098 | TTATTGATTCATTTA[C/T]ATAGTAATTATAGCT | 5521 |
rs141049802 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929888 | TAGAATTAAGATAAT[A/G]TAAGTAAAGAGGGCC | 5521 |
rs141050687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854371 | TATAATGATCAAGTT[A/G]TGGTATTCGGGTTAT | 5521 |
rs141056203 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892717 | TGTTCTGGGAAAAGA[C/G]GTGCAGTTTGAAAAA | 5521 |
rs141074232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071795 | CCACTTGTTTATTAC[A/G]TCTATTGTCTAGCCC | 5521 |
rs141081215 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932341 | CAAATCTCATCTTGA[A/G]TGGTAGTTCCCATAA | 5521 |
rs141082923 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006832 | TTCTTAGGGGAAGAG[A/T]GTTGTTTTTACACTA | 5521 |
rs141087320 | in-del | -/ACAC/ACACACACACAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053545 | TTGCCAACAATATAA[-/ACAC/ACACACACACAC]ACACACACACACACA | 5521 |
rs141103213 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624823 | CCTGCCTCCTCTCAT[C/G]CTATTCCTCCTTATG | 5521 |
rs141111824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017869 | TCCTGTTGCTTGTCT[A/T]TCCTAACAAAATTAA | 5521 |
rs141130579 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617241 | GGGCAGGGGGAAGTG[G/T]GTTAATGGTTAATGG | 5521 |
rs141143608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971355 | CAAGAAAATATAACA[C/T]GTGTCCCCTTCTCTT | 5521 |
rs141158066 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624124 | AAACCCTGATTTCCT[C/T]AGCTGCAAAAAGGAA | 5521 |
rs141158778 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757932 | CATGCACCTTGAAGG[C/G]TTGGTCGCCTGAAAT | 5521 |
rs141171365 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820614 | TGGGGATATTTTCTT[C/T]CCATTACTATTCCTC | 5521 |
rs141171401 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863858 | AATTGAGATTTCACA[C/T]CGACTCCCAACTGTA | 5521 |
rs141175428 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751481 | CTCTTCTCTCCTTAT[A/T]CCTGTCTTCTTTCTG | 5521 |
rs141189370 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928222 | CTTTGGTGATTTCAT[C/T]GATTTTCATGATTTT | 5521 |
rs141192534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725920 | GAAGCTGAAAATTAT[A/G]ACAAGAAAACTATGA | 5521 |
rs141196787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645341 | AAAGAGGACTCCAAG[A/G]GATATTCCTCTCTTA | 5521 |
rs141197426 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903946 | AGATTCTTCCCATTT[C/T]ATGACTAACATAATG | 5521 |
rs141199085 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037867 | CTGTACTCTCCAGGG[A/G]CTCTGTTTTATTTAC | 5521 |
rs141201955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977164 | CATCATTTTTCACCC[A/C]CCGACAAGGTCCAAG | 5521 |
rs141211761 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051310 | ACATGGAGACAATGG[C/T]GTTTAATAAGACTGT | 5521 |
rs141216745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931300 | GTTATTCTTCTGCTA[C/T]ACAATGGGAAATGGA | 5521 |
rs141218637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927142 | AGTGATGTCCCATGA[C/T]TTTTAAAAAATAAAC | 5521 |
rs141220932 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861221 | CCACCACGCCCGGCT[A/G]ATTTTTTTGTATTTT | 5521 |
rs141225294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764855 | ACACACGCACACGCA[C/G]ACGTACTCTGCCCCA | 5521 |
rs141234395 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860005 | TCTTATTGGAGAGAT[C/T]CAACCAAAAGGTATA | 5521 |
rs141234884 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710494 | ATTTTCCCATAGTTG[C/G]AACAAAACTTGCCTA | 5521 |
rs141246734 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629916 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTACCTCA | 5521 |
rs141267776 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821402 | TAGATCAAGCTCAAA[G/T]CATGAGCCCACCCTC | 5521 |
rs141272706 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597953 | CTTTGCTCCTTCAGC[A/G]GTCTCTCTCTAATGG | 5521 |
rs141274669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991657 | TCAATTATTATACCA[C/T]ATACACAAGCAATGA | 5521 |
rs141284379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919118 | AACTTGCCCAAAGAC[A/T]TAATTAGCATATGGT | 5521 |
rs141291124 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711978 | TTTTATTTCTCTAAA[G/T]GACAAATTGAACACT | 5521 |
rs141293888 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799915 | CCCATGTATACTAAC[G/T]GCTGATGTCTCCATG | 5521 |
rs141309195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923573 | TGTCGGAAGCCCTTC[C/T]TGGGTTTCACAAATA | 5521 |
rs141319263 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824055 | CCACTGTCATCTTCT[C/T]CACTTATAAGCAGCT | 5521 |
rs141321199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755746 | AAGTAAACTTTGTAT[C/T]GGATTTCTTTTAGGC | 5521 |
rs141327822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870681 | GGTACTCTTCGCCAC[A/G]CTCCGTCCAACAGAC | 5521 |
rs141336386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718134 | TTTTTTTTTAACCAA[C/T]GGTATTCCTGGCCCC | 5521 |
rs141340093 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906928 | AATTTAAAGAGACAA[C/T]CTACTTCTAAGAAGA | 5521 |
rs141340366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865625 | CAGTGCCTAATATAT[A/C]ATAAATGTTTTTAAA | 5521 |
rs141341822 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986070 | CTAAAGAAATCAGGT[A/G]AGAGATCATACTACC | 5521 |
rs141365470 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873895 | CAGACTCCATTCTCA[-/T]TTTTTATCACTCTTC | 5521 |
rs141366875 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638785 | AATGATTAAGGTACT[A/G]GTCCTATTATAACCA | 5521 |
rs141374940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031459 | TTTAGCAGTTCTACT[A/G]TGATGTGTCTAGGCA | 5521 |
rs141393891 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744033 | ATTTATTCATACCAT[A/G]CCTGGAAATTATAAA | 5521 |
rs141400658 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989392 | ACACATTAGAAAGAT[C/T]ATTTATTATGATCAA | 5521 |
rs141408821 | in-del | -/AAG | 0.405429 | 0.195811 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005803 | AGAGAGAGACAGACA[-/AAG]AAGAAGTCAAACAGA | 5521 |
rs141418337 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850760 | GCAATTGTACATTTA[C/T]CTTTATTATTCTTTA | 5521 |
rs141419491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921541 | TGACACTTAAGATTT[C/T]GTTTCTTAGAGAGAC | 5521 |
rs141430342 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690046 | TAATTAAGCATACAA[C/T]GACCATCCCATTTTG | 5521 |
rs141430735 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025876 | AATAAGAACATAAAA[A/C]GATACCCTGCTTCCT | 5521 |
rs141444177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686086 | GCTCTTCCGTTTTCT[A/G]GCCATGAGATTTTGG | 5521 |
rs141447016 | snp | C/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589716 | TATGGAAGAATTACT[C/G]TTAGCTGGCAGCTTT | 5521 |
rs141452925 | in-del | -/T | 0.0640965 | 0.167152 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022398 | CTGTCTCTGCTAAAA[-/T]TAAAAAAAAAAAAAT | 5521 |
rs141456452 | in-del | -/T | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687514 | ACCCGCATTTTCACC[-/T]GCTAAATACCTGTCC | 5521 |
rs141470967 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623166 | GGCCCCACAGTGACA[C/T]GAACACAAAAGATTC | 5521 |
rs141491104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687492 | AAATGATCAATAAGT[A/G]CTAGATACCCGCATT | 5521 |
rs141492627 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699431 | GGTTCTTTATCCTCA[C/T]TGACATTTATTTTTT | 5521 |
rs141497813 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808080 | TGCTAGGATTACAGA[C/T]GTGAGCCACCGCACC | 5521 |
rs141502968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603539 | TTATTTGTGGAGTGC[C/T]GGCTTTAGGTAGCAC | 5521 |
rs141503802 | in-del | -/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963393 | GAGGGTGAAGTGAGG[-/T]TTTTTTCTCTCTTTC | 5521 |
rs141513059 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977840 | GCAATAAACATACAC[A/G]TACATGTGTCTTTAT | 5521 |
rs141515158 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880521 | GAAAAGCTAAGTTCA[C/T]CTCTTAGTGAATCAA | 5521 |
rs141529561 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999083 | TGTGCAATTCTTCAG[A/G]CCTATATAATTGTTT | 5521 |
rs141546613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800788 | CTCCAAGGAAGTGAA[A/C]TCAGGATCTCCAAGA | 5521 |
rs141546924 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019883 | GCTATGGGAATACAC[C/T]GCTCAGATCTCGTTT | 5521 |
rs141560613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866388 | GTCTGCTGATTGATA[C/T]TGGGAAAGATGACAC | 5521 |
rs141567663 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649599 | ACAGGCGCCCGCCAC[C/T]ATGCCTGGCTAATTT | 5521 |
rs141569538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043096 | AGTGATAATATATTA[C/T]ACACCTGTTCTTAGT | 5521 |
rs141572124 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077908 | CGTGTATTCATAATG[A/G]TCGTCTAAGGGCATA | 5521 |
rs141580237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600987 | TACTAGGTAAACACC[A/G]TCTACTTTCTGATTC | 5521 |
rs141583594 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003317 | GACCAAAAAAACCCC[C/T]GGGCTATAGGTTATG | 5521 |
rs141585639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958955 | CATCCATTTAGTAAG[C/T]AGTTGGAGGTGGGAT | 5521 |
rs141597780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891427 | CTGTCATTGTCTACA[C/T]GGATGCTAGATTTAT | 5521 |
rs141599094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770746 | TTGGGACTTGAGAAT[A/G]CATGGGAGCTGTTAT | 5521 |
rs141602474 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694980 | TGCATATATGATTTA[C/T]AATAGTGAGAATTTG | 5521 |
rs141639451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795275 | TTCACAATAGATAAG[A/G]TATAGAAACAACTTA | 5521 |
rs141641219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690905 | GCCATGTGGGCAAGT[A/C]TTCTGGGACAAAAGG | 5521 |
rs141649430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608146 | GAGGGGTAGGAGGGG[G/T]CATCCTATCTAGACA | 5521 |
rs141651279 | in-del | -/C | 0.137378 | 0.223195 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011300 | TTAAAATTATAAATG[-/C]CCCCCCCATCCCTAC | 5521 |
rs141651515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000831 | TCATCTCCTGAGGGA[C/T]TTCCCTCCTGACTAG | 5521 |
rs141651691 | in-del | -/TTGCCATTGAGGAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016558 | GAAAACATAGGGGAC[-/TTGCCATTGAGGAG]ACAGTCACATATACA | 5521 |
rs141660474 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081551 | GAGGCAGTTCGTTAA[C/G]GGGTGAGAGGAAAAG | 5521 |
rs141664043 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897339 | TAACTCTTCTCATCA[C/T]ACCCTGGGTGGATAC | 5521 |
rs141664426 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814038 | CAGTGGATTGTGGCA[-/G]GTTAAAGCCATGACT | 5521 |
rs141668595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606513 | TAGTAGTACCTATGT[C/T]CTAGGGCGGTTGTGA | 5521 |
rs141673303 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686734 | TCCCAGGGCACTGGC[A/C]GCTGATAATAATGAG | 5521 |
rs141676115 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890041 | ATCCGCACACACACA[A/G]TGGCTCTTCTTAACT | 5521 |
rs141678464 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602143 | CTCTGAAGCCCTATC[A/G]TGCTTGGTCTGGTCA | 5521 |
rs141678533 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079996 | ATATAATTTTATATG[A/G]ATTTATTTATTAATT | 5521 |
rs141690954 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008644 | TAGCTCAAGAGTCAC[C/T]TCTTCTAAGAGGCCT | 5521 |
rs141697196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787407 | GTTTTTCAAATGTTG[A/G]CAGCTCATTTAAAAT | 5521 |
rs141706391 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784921 | TACAAAGGAATAAAA[C/T]AGATGGAGTATCAAC | 5521 |
rs141709337 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749245 | CCCATTTTCTAATTG[C/T]ATTTTTTTAATGCTG | 5521 |
rs141716970 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672190 | CAAGGAGGCAAGAGG[A/T]GATGTAAATTTCCCA | 5521 |
rs141735311 | snp | A/G/T | 0.00637319 | 0.05614 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850893 | CTGAAAAATGACCAC[A/G/T]CAATCTATCCATACT | 5521 |
rs141740797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856253 | TATCATCCCCATGTA[C/T]ATTTGGTCAAAATAT | 5521 |
rs141742935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791079 | GGAAGGACTCAACTA[C/T]GCCCAGTCACCTATC | 5521 |
rs141746510 | in-del | -/GAGTGACCGAGTATTACGGAGAAAGG | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590247 | GGCAGAGAGCAAAGG[-/GAGTGACCGAGTATTACGGAGAAAGG]CAATGACATATCTTC | 5521 |
rs141759488 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955424 | AGTAAATAGGGCACA[C/G]CATTCAGTTATACAA | 5521 |
rs141764083 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960356 | GTGCAGTGGCACAAT[C/T]TCGGCTCACTGCAAC | 5521 |
rs141768658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893232 | TAACACCTCTAAAGA[A/G]CTTCATATACAAAAA | 5521 |
rs141775292 | in-del | -/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881068 | GCTGGGGGGCGGGGT[-/G]GGGGAGAGAGTGGGG | 5521 |
rs141794206 | in-del | -/AAAT/AAATAAATAAAT/AAATAAATAAATAAATAAAT/AAATAAATAAATAAATAAATAAAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886340 | GAGACTCCGTCTCAA[lengthTooLong]AAATAAATAAATAAA | 5521 |
rs141814533 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781787 | CCAGACTAAATCCAA[C/T]TGAAAGTCAAATAAA | 5521 |
rs141819361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705302 | GGTTTTGGTAGTTTT[C/T]GCCTTCAGCTAAGAT | 5521 |
rs141830838 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876093 | TTTGAGTGTGATTAG[A/T]ATGTGTGTGTGTTTG | 5521 |
rs141831559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943776 | TCCAAATCCAGCTTA[A/C]TGAAACAAGCACTGT | 5521 |
rs141837581 | in-del | -/TTTGGC | 0.467234 | 0.12373 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644307 | GAGTTTTAAATTGTT[-/TTTGGC]TTTGGCTTTTAAAAT | 5521 |
rs141846352 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890257 | CCCTTGCCTCTGCTT[G/T]TAAGCCCTGTGATGG | 5521 |
rs141847573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817633 | AACTAGGGTTTTTAA[C/T]GACTAAAGTAACATA | 5521 |
rs141849148 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670273 | AAACTGGCTTTTAAA[A/G]AAATCAGAATCACCT | 5521 |
rs141854843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069434 | TCCTGAAAGCTTCCC[A/G]TTGTACCCAGAATAA | 5521 |
rs141863713 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986803 | ATGTAAGAGTCATTG[A/C]CCTTAAAGTCGGAGT | 5521 |
rs141867350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665901 | GACATGAAATGAGCA[C/T]ATGCTGCTCGAAAAA | 5521 |
rs141879288 | in-del | -/TT | 0.0441095 | 0.141807 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072202 | AATATCTAAACTAAC[-/TT]TTTGTCTGCAATGTG | 5521 |
rs141880750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855276 | GAAGAGCTGAACTCT[A/T]CCTCACATCACCAAC | 5521 |
rs141896573 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744503 | CTTTCAGAATGAACA[A/G]TGGGTGGAAAACACT | 5521 |
rs141903203 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906003 | GAAATAAAAGTTATA[A/G]TGGAAAGCTTGTAAG | 5521 |
rs141905659 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743123 | AAACTAATATAGTAA[C/T]ACACAAACCAGGTCC | 5521 |
rs141916832 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660153 | AAAGCAACCTGGGGG[G/T]CAGAGTCTGGCATTG | 5521 |
rs141924065 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775898 | ATAAAAAATAATAAA[A/G]TGCTTAGGAATAAAT | 5521 |
rs141924598 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712755 | CACAATGGGTTGAAG[A/T]GCATGATCATCCCCA | 5521 |
rs141924617 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667665 | AATAGAACAGGGACT[C/T]GGCAAGCTGTTAGGA | 5521 |
rs141935209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980782 | ACATGCATAGGAGAA[C/T]TGCTTTCTCTAATGT | 5521 |
rs141938427 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938915 | CCTCCTGAGTAGCTG[A/G]GACTACAGGCGCATG | 5521 |
rs141943513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842954 | AGAACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 5521 |
rs141959872 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063385 | AAGTTAATGGAATTA[A/T]AAAACATATTTTAAA | 5521 |
rs141962233 | snp | A/G | 0.00133348 | 0.0257868 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590061 | AAAGTCCAGACTGTC[A/G]ACACTGATCTCGTCT | 5521 |
rs141979103 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786419 | ATTATGAAGTTGGCA[A/C]CTTCCTGATTATCCC | 5521 |
rs141990632 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901828 | TGTGATGAGTGGTTG[C/T]ATTAGAAGGAAATGG | 5521 |
rs141996428 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939375 | GACCCTGAGCACATG[A/C]AAGTCACGTTCAAGG | 5521 |
rs141999179 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069497 | CACCTGAACCTGCCT[C/T]TGCTTCCCTCCACAA | 5521 |
rs142003164 | snp | G/T | 0.127944 | 0.218179 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608615 | ACCTGGCCAATATGG[G/T]GAAACCCCATCTCTA | 5521 |
rs142009286 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654066 | GGCAGGAAGGAGATC[C/G]GGACACTATTCCCTG | 5521 |
rs142023448 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829913 | GTTTCATGTTTGCCT[C/G]TTACTAGTTGTGTAA | 5521 |
rs142027916 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985043 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGT | 5521 |
rs142032852 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735782 | ACCCACATTCAGAGA[C/T]ATAGCAGCAGGATCC | 5521 |
rs142042792 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637726 | AAGCCACCAGCTCCT[C/T]CCCCCAGCTGCTGTT | 5521 |
rs142045480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671369 | CTCCCCATTAAGAAC[C/T]GCTAAATGGTGGGTT | 5521 |
rs142046982 | in-del | -/G/GAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936468 | CCTTGTAAGCAGGAA[-/G/GAG]AAGAAAAAAAAAAAA | 5521 |
rs142051322 | in-del | -/TTGT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861854 | CTTTAAAATACAGCA[-/TTGT]TTTTTTTTTTTTTTG | 5521 |
rs142057998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815358 | CCTGCACACACTTTC[A/G]TTGTATGCTTATTGA | 5521 |
rs142058250 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746766 | AAAAGCAGCACATCT[A/G]AATGGTGGCTATTCA | 5521 |
rs142059715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982287 | CATTCCATTTCATAT[A/G]TTTATTTTCCTCAAG | 5521 |
rs142063265 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852375 | CAAATCATAGCCTGA[C/T]TACAGGTCATTAGTG | 5521 |
rs142078310 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028883 | TCTGATCAGTATGTC[A/G]TGGTATTCCATTGTG | 5521 |
rs142081241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669821 | TCGGGATCAGCAGAA[C/T]TAGGATTCAAATACC | 5521 |
rs142081326 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062164 | AAATGCTTATCATTG[C/T]GTTACAACTGCCCAG | 5521 |
rs142087016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923020 | GCCAAGAAGAAAAAT[A/G]GAAAAAAGTATTTCA | 5521 |
rs142092546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871770 | TGCCAAGAATCCACA[C/T]AGTCATGAGCTCTAA | 5521 |
rs142121915 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904734 | AGCAGAAACAGTTAA[A/G]AACACAGTGATGAAC | 5521 |
rs142132225 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835756 | GTACTGTACAGATAT[C/T]GGTAAAGGAGTCATC | 5521 |
rs142132797 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701691 | GCTCCAGCTTGGCCC[A/G]TGCCCCTTCTTTTTT | 5521 |
rs142158402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881890 | TTGTGAGCTGGAAAT[G/T]TTCTAGCTCATAAGC | 5521 |
rs142159537 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809000 | GTGTGTGTGTGCGCG[C/T]GCACCCACTTCTCCA | 5521 |
rs142169229 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940804 | TCCACTGAATTCTCT[A/G]TCATATGAGCATCCA | 5521 |
rs142184357 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874104 | TCTAAATTAGATCCA[C/T]CTTTCCACCTTATGA | 5521 |
rs142189262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943485 | TCTCTCCCATTCAGC[C/T]CATGAGGTTGTAAGA | 5521 |
rs142193382 | in-del | -/AAATAAAAGATAAATAT | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800191 | TTTTCTGTAATTTCC[-/AAATAAAAGATAAATAT]AAATAAAAGATAATA | 5521 |
rs142202392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869682 | AGGAAAGTGGGATGG[A/G]CATGGGATGGAGGGT | 5521 |
rs142205607 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763385 | GTTTCTCAACCTCTC[-/T]GAGCCTCTGGTTTCT | 5521 |
rs142208385 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652183 | CAGATTCACCACTAA[C/T]CAATAGGCTATGAGG | 5521 |
rs142212876 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907920 | ATCAAATGTTGGCAG[A/C]ATTGAATTCCCTAGA | 5521 |
rs142221512 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059229 | ATATGGGCTATGACA[C/G]CAGGAAGAGGATACG | 5521 |
rs142222113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730711 | CACCATGTAAGAAGT[A/G]CCTTTCACCTCCTGA | 5521 |
rs142233065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980111 | TGTTATGGAGAGATG[A/C]CAATGATATATTTTT | 5521 |
rs142234014 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773507 | TTGGTTGAAACAGAA[G/T]GCATTCTCCATTGTA | 5521 |
rs142272335 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839016 | TTTGATAGGCTGAAC[A/C]CTAGAAAATTCGTCC | 5521 |
rs142274068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798373 | TGGTAATTTATTTCT[C/G]TAATCCACAGCTTCC | 5521 |
rs142283108 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644847 | ACATATTTCTCCAAG[G/T]ATAGGGTTTATATGC | 5521 |
rs142302356 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898321 | TTTTGGTTACTGTAG[C/G]CTTGCAGTATAGTTT | 5521 |
rs142304297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966154 | AGTTGGTGTTCTTAG[C/T]TAATGGTCCTTTGGC | 5521 |
rs142311167 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837478 | TGGGAGAAGAAAGTG[A/C]TGTGGCTATAAGGTG | 5521 |
rs142314071 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767857 | CATATACAGTAGTTC[C/T]ACCACCCTAAAAATG | 5521 |
rs142314157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725169 | GGAGCCTGGAGAGCA[C/T]ACAATTTCAAGAAAA | 5521 |
rs142317741 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694536 | TCATGGGTATAACAT[A/G]AAGAATAAAAATCAC | 5521 |
rs142317785 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646070 | CATTCATAGAACCAT[A/G]TTCCCTGTCTTCACA | 5521 |
rs142320073 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081324 | AGTCTGCAAGTACCA[C/T]GTCCTGCTGTGAATC | 5521 |
rs142331169 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960450 | GCAGGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 5521 |
rs142333123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039909 | GGACCAACAAATGGC[C/T]CAACACTAAATTTCC | 5521 |
rs142361548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009966 | CCATTCTAACACAGA[A/G]GTGTTGTGACTATTA | 5521 |
rs142364730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801955 | GGAGCAGCTGCATGT[A/G]TCTGTCATTCAAATC | 5521 |
rs142372277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766028 | GTGATACCTAAACAT[A/G]TTCTTTTAAAGGAAA | 5521 |
rs142383244 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642898 | CCTATCTCTACCAAA[C/T]ATACAAAAATTAGCC | 5521 |
rs142386331 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035541 | GACTCTCAAGGCTTT[C/G]GGTTCAGGAAAATCA | 5521 |
rs142397059 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921099 | ATTCTAGAGTGAATA[A/G]CCTCCAAATGTTAAT | 5521 |
rs142402696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750969 | CCACAAAGCAGCACT[A/G]TTCTGCTCTCAACAG | 5521 |
rs142413797 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762571 | AGTAGTTATTTCTTA[C/G]ATATCTACATACTCT | 5521 |
rs142416681 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689465 | AACACAGGAACAGGC[A/G]TACAGGTTTGTAGCC | 5521 |
rs142417263 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046280 | AAAAAGTGACATTCT[C/T]GTGTATCAACAATAA | 5521 |
rs142425394 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922470 | TGTAAGCTAGATGGT[A/G]GGAAGCAGCCTAGTG | 5521 |
rs142427986 | snp | C/T | 0.0170251 | 0.090679 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858529 | TCTTCTTATCAAAGA[C/T]TTCACTGCTTACATA | 5521 |
rs142437131 | snp | G/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962434 | GAGACCAAGGCGGGT[G/T]GATCACGAGGTCAGG | 5521 |
rs142438071 | in-del | -/G | 0.0577344 | 0.159793 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010305 | CCACAGACTGGGGCA[-/G]GGTGGAAGGGGGAAT | 5521 |
rs142449843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647961 | CATTGTCTCCAAATA[C/T]ATCTCATAATTGCCA | 5521 |
rs142450432 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896689 | CCATTTCTTTCTTCC[-/T]TTTTTTTTTCGGTGA | 5521 |
rs142456219 | in-del | -/CTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000691 | CAAAAACCACAATTA[-/CTT]TTGCACCAACCTAAT | 5521 |
rs142458208 | in-del | -/AACA | 0.00886186 | 0.0659727 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000079 | GATGATGGTGACTTT[-/AACA]GACAGAGGGATTCCA | 5521 |
rs142461558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648916 | ACAGGTTCCAGATCA[C/T]GCAGAATCTTATAGG | 5521 |
rs142461655 | in-del | -/GCT | 0.368938 | 0.219895 | intron-variant, utr-variant-5-prime, cds-indel, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878727 | ACGCGCGCACTCGCA[-/GCT]GCTGCTGCTGCTGCT | 5521 |
rs142472590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849963 | ATCTCACACTTCTAG[A/G]AAGGAAAATAAGACC | 5521 |
rs142476946 | in-del | -/TTAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827436 | CCAGAACACATCGGT[-/TTAA]TATTTTCAAAATGTC | 5521 |
rs142481790 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042081 | TCCCAGGAATTCGTC[C/T]GATTGATAACGCCCA | 5521 |
rs142487098 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816787 | GACCCATATGGAGGA[C/G]CTGATTCCAAAATCC | 5521 |
rs142490438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677982 | GACAGAAGGAAACAT[C/T]TGTGAACAGTGATTT | 5521 |
rs142493630 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071425 | CAGGCAGGAGTCCAG[C/G]TATTTATAATGGTTT | 5521 |
rs142494366 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595373 | CTGCTTTGTGATGAA[A/C]CTTTCCTCATCTGTC | 5521 |
rs142502065 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848726 | AACTGTACTCTGCAC[C/T]CTTAGAAAGAAGTCA | 5521 |
rs142505263 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783537 | TTTCCATTTTCCAAA[G/T]TCCATACAACTTTTA | 5521 |
rs142523490 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721672 | GCACTTCCTTCTATG[C/T]GGAAGCTCCCAGTGA | 5521 |
rs142528788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988974 | AACTACTATGAACAA[C/T]TACACGTAAATAAAT | 5521 |
rs142535319 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892419 | GCAGGCTACAAATAG[C/T]TCTTGCTAAGTGTCC | 5521 |
rs142540225 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891019 | GGTACACAGTTGAGT[G/T]CAAGTTTAGAATTAC | 5521 |
rs142541142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923168 | ATTTTCTCTGACTTG[A/G]CACTAAAAGATTCTC | 5521 |
rs142575996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945518 | TCCGATATATTGACT[A/G]CCTTGCTCCCCACTG | 5521 |
rs142583571 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663203 | AGTACACAACTAGTA[C/T]TTGCTGGAGCTGAGA | 5521 |
rs142597798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066018 | ACAGGTTCCTGATTC[A/G]GGCTGGAATCAAACC | 5521 |
rs142606978 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924379 | ACCATCTTCACCAAA[A/G]TATAATGGTAGCTGC | 5521 |
rs142609375 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913682 | TTGAAAAACATAAAC[G/T]GAATTGAGAGATGCA | 5521 |
rs142613006 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000428 | CTTGTTCCTGCTCCT[C/G]TAAATGTGTTCTGCC | 5521 |
rs142617603 | in-del | -/AAATT | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851656 | TATACTCACTTTCTC[-/AAATT]AAATAAGTGTAGGCA | 5521 |
rs142626429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658285 | CTTGAGGCACTAGAC[A/G]GTAAATCTCTCAGAG | 5521 |
rs142628394 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708066 | TAAAAATTTAAAATT[C/T]ATATATAGGCTGGGC | 5521 |
rs142634233 | snp | G/T | 4.948e-05 | 0.00497369 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638284 | ACAGGGCAGATGCCC[G/T]CATGTCACACAGCCG | 5521 |
rs142635447 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893710 | CACATACCAGAGGCT[G/T]TCAGTGGGTGGGAGG | 5521 |
rs142645383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710035 | CTACCACACAACCAA[C/T]TTTCCTTCCCACTTG | 5521 |
rs142656298 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832342 | AAAGCTCCATTCATG[C/G]TAAGTGCCCTACACA | 5521 |
rs142663325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819598 | CTTTGGAATAGTTAT[C/T]GTTTCCTCCATAAGA | 5521 |
rs142664443 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779949 | CGAATTTTGGTTTAT[A/G]TTAGATTTGGAGATT | 5521 |
rs142670521 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616809 | TATGAATAACAGTTT[C/G/T]GAGATTCCTCAAAAA | 5521 |
rs142690193 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699863 | GTGTAGTATGTGCCA[A/G]ACCAATTAGCACTAG | 5521 |
rs142694496 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901034 | ATCCAGTCTGTCATT[A/G]ATGGGCATTTGGGTT | 5521 |
rs142694962 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016774 | TCTATCCAGGCAGAA[A/G]ACATGTCATAATAAA | 5521 |
rs142697000 | in-del | -/TC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675821 | CCAACCTCAGTCACT[-/TC]TCTCTCTCTCTCTCT | 5521 |
rs142697455 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821037 | TCATTCCGCCTCCTT[A/G]ACAGTGGTACATTCA | 5521 |
rs142701257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782123 | CATGACTGCAAGTTT[C/T]CTGAGGCCTCCCCAG | 5521 |
rs142702018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897503 | TCTGTGCCTACTCAC[C/T]GTATAATGAAACCCA | 5521 |
rs142702827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825996 | TCTTATGAGTTATAG[A/T]TATAAGAAGAATTTC | 5521 |
rs142706806 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940102 | GTCAAGAAGAGATGA[A/G]TTAGCATTTGGTGAA | 5521 |
rs142722206 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806123 | GTGTGCCACTGAACA[C/T]ATGAAGAAGCTAGGG | 5521 |
rs142724393 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737279 | TTCTAGTAGTATTTT[C/T]TGGGTGTCTACTTCA | 5521 |
rs142740224 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677572 | GAGACAGGGTCTCAC[C/T]CTGTCACTCAGGCTG | 5521 |
rs142771369 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793964 | ACCATGCCTAGACAT[C/T]GATTCAGTAGATATT | 5521 |
rs142774688 | in-del | -/ATAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886359 | AAATAAATAAATAAA[-/ATAA]TAAATAAATAATAAA | 5521 |
rs142785050 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756563 | GGTAGCCTCTGGGAT[C/G]CCTGGGTTTGAATCC | 5521 |
rs142787326 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682074 | AGACAAAGAGAACTC[A/G]ATCCTAAACCAGGTA | 5521 |
rs142817647 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797659 | CACATTATTGTCATC[A/C]AATGGTATTTATTGA | 5521 |
rs142822986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074207 | AAATTATTCAGTATC[C/T]TGCCTAAGGTCACTA | 5521 |
rs142825661 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025399 | AGAAGAAAGAAACAA[A/T]CCCTAACATGTTATA | 5521 |
rs142831846 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906092 | TCTAAATAAAAATTA[A/G]GTATTTCTAGTAAAG | 5521 |
rs142844578 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931184 | TAACGCAAGCCAGAA[A/C]CTTCCGCAATAATAC | 5521 |
rs142845229 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952910 | GCAAATGAATAGAAA[C/T]AGCAGATAATAAGTG | 5521 |
rs142847118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032458 | TTGGTTCACCTATCA[C/T]CCAAGCAGTACACTC | 5521 |
rs142855014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836461 | GTCCCAAATTGCAAC[A/G]AACTGGACTCCACTT | 5521 |
rs142860069 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646812 | GTCCTGTTTACTGAG[A/C]ATTTGCTTAGCAAGG | 5521 |
rs142860272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633149 | AGTGGTAGAAAAAAA[C/T]AGGCGAGGGAGAAAA | 5521 |
rs142867299 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005073 | CACTACTCCTTGAGG[A/G]ACCAGTGCTTCAAAC | 5521 |
rs142868502 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020321 | ATATTTATATGATTA[C/T]TTAATAAATAATTTT | 5521 |
rs142873962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052353 | GCACCTATAATGTGC[C/T]TGGTATTGTTCTGGT | 5521 |
rs142883727 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639793 | TTAGCTTTATCTAAA[C/T]AGTAACCCAATGTTC | 5521 |
rs142902004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709403 | CTTTCTTCCTTGCCT[G/T]CCTCCTACTGTCCCA | 5521 |
rs142905554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599703 | GTGCAGAACATGCAG[A/G]TTTGTTACATATGTA | 5521 |
rs142918973 | snp | A/C/T | 0.00279242 | 0.0372774 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026296 | CAGCAATAAAAAGAT[A/C/T]GAACTATTGCTACAC | 5521 |
rs142919113 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078493 | GGGTAAACTCATTAA[A/G]ACACATTGTATTGGC | 5521 |
rs142919641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789059 | TCAAATATGTTGGAA[C/T]GAACTCAGGTCCCTA | 5521 |
rs142934009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728654 | TGTTGTGGGAGGGAC[A/C]CAGGGGGAGTTAATT | 5521 |
rs142947746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872251 | TTCAATGCATTCTGG[A/T]TATTATGTTTAGTAG | 5521 |
rs142949894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801331 | TATTAAGTGTTCTTG[A/C]CATATATACACAGAA | 5521 |
rs142954266 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001282 | AATAAATCTTGCTGC[C/T]GCTCACTCTTTGGGT | 5521 |
rs142973526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952827 | AACCTTGGCTGCTAG[A/G]TATGTGAGAGTCATA | 5521 |
rs142995355 | in-del | -/G | 0.0199302 | 0.0978156 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591149 | TGGTTCCCCTGGAGT[-/G]GGGGGGCTCCTACTC | 5521 |
rs143007916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981947 | CCTCTGCAGCAGTTG[G/T]CCCAGGTGGTCAGCA | 5521 |
rs143038021 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618971 | CAGTGACTCTGTGTG[A/G]CTGATAGCCAACAGT | 5521 |
rs143038728 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692073 | CTGTCTCTTTCACTA[A/G]AGTGTAAAATTGTTG | 5521 |
rs143041692 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947987 | AAAGGCATGCACTCA[G/T]GAGACCACAGGGTTG | 5521 |
rs143046069 | in-del | -/ATA | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742645 | ATATAATAATAAATG[-/ATA]ATAATTATTATGGGT | 5521 |
rs143057627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874221 | ATCTCCTTTGCTAGA[C/T]TGAAAGATCCCTGAG | 5521 |
rs143060662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803434 | AACATTAAGTTTAAA[C/T]TCAGAACTGAGAACT | 5521 |
rs143079109 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970795 | TTGAGGAGTTGCCCC[A/G]TAAAACTTACAGTCA | 5521 |
rs143091180 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881307 | TTTTCTGCCTCCACA[-/T]TTTTTTTTTTGTCTT | 5521 |
rs143092753 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875222 | ATATATTGAAATGCT[A/G]TACATAAAGAGCTCA | 5521 |
rs143093711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654595 | GGAGGCCATAGTGTC[C/T]AGGCCTCTCCTCCTT | 5521 |
rs143095076 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762493 | TCTTTCTATTCAAGG[C/T]GCTGTGCTAAGATTT | 5521 |
rs143106850 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644960 | TCCTGTCTAAGCCAA[G/T]GGAGGATAAGAGAGC | 5521 |
rs143114732 | in-del | -/TCAA | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589545 | TTTTGTTGATTTTTT[-/TCAA]TCAATCAAATGGAAT | 5521 |
rs143133271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763940 | CTATATTGCACAGGC[A/T]AGTCTTGAACTTCTG | 5521 |
rs143138464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690328 | CGCTTTGAGAAATCC[A/G]TTTTTAATGCCACTT | 5521 |
rs143139744 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887350 | CCATTTGCAAAAAGA[A/G]TTTTAATGTGTTCTT | 5521 |
rs143141208 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843133 | CGGAGGTTGCGGTGA[A/G]CCCAGATCGTGCCAT | 5521 |
rs143145222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776225 | AATAAAGTTGGAGAA[C/G]TCACATTTCCTAATT | 5521 |
rs143154447 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860224 | AGCCATCATGCTATT[G/T]TAAGTATACATTTTC | 5521 |
rs143169354 | in-del | -/AG | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753354 | TACTCTCCCACACAC[-/AG]AGAATAGACAGTATA | 5521 |
rs143170240 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739491 | ACTCATAGAACATGG[C/T]ACATTTGGGGACCAA | 5521 |
rs143174656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045676 | AATGTACACCCCTCG[A/G]TAATTTACAGTTGCT | 5521 |
rs143178421 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659559 | AGGAGAACTTAGCAT[A/C/G]ACGATTGACACATAC | 5521 |
rs143180295 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963501 | TTGGAATTTCTTATC[C/T]TTTTGCCCTGCAGAA | 5521 |
rs143193314 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996816 | CTCAGGAGGGATCAA[G/T]TCTCCCTCCCACTGT | 5521 |
rs143197322 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950478 | TTGGCAGCACAGTGA[A/G]TCACCTGGAAAGACC | 5521 |
rs143203348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080295 | ACCTGTGTTATACCA[C/T]ATCTGGAATCTAAAC | 5521 |
rs143205537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883186 | TGACCTTTGGTGAGT[A/G]GTTTAACATCTCTGA | 5521 |
rs143207362 | in-del | -/GG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966317 | CACATGGAAGAGGCT[-/GG]GTTGTGTCCATCTTG | 5521 |
rs143212822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681098 | CCGGCTTGCAACGTA[C/T]TAGGATCAAAGTGAT | 5521 |
rs143212961 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073405 | AGAAAAAATGCTTTC[A/G]TCTTGCACAACTTGT | 5521 |
rs143212984 | in-del | -/TTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976123 | TTATTATTATTATTA[-/TTG]TTATTATTATTATTA | 5521 |
rs143216201 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597122 | CTTCCTGCTACCTGT[C/T]CTTCTTTCAGCCATC | 5521 |
rs143231360 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786059 | AACATGAAGGAATAA[C/T]AAAATCTTTGAGGTG | 5521 |
rs143232914 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780306 | CATTAAATTATTTTT[A/T]AAAATGGGCAATGTT | 5521 |
rs143236923 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736492 | TAACTTGCTCCAGAT[C/T]GTGCAGGAAGAAATG | 5521 |
rs143238322 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796309 | TCACAAACAGAAGTC[A/C]TCACAAAGGACAGAG | 5521 |
rs143245680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724907 | GATGATTGACAGTTA[A/G]GAAAGGGAGAACACC | 5521 |
rs143249297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052067 | AGGAAAGACAGTCCA[A/G]TCCTCTTTGCAAAAC | 5521 |
rs143256063 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960694 | CAAATTAGATTCTGA[A/G]CTCTGGTTAATGTGT | 5521 |
rs143276251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743476 | AAGGTGAGGTGGCTG[C/T]TACTCACCTAATGAG | 5521 |
rs143284945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955995 | CGTTGGTCAGGCTGG[C/T]CTCGAACTCCTGAAC | 5521 |
rs143299931 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850447 | TATTTTTGCAAGACT[A/C]TGCAAGATGTGGCTT | 5521 |
rs143310808 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621249 | TTAAAGGTTCCTGGA[A/G]TTTGCAAACATCGAG | 5521 |
rs143311335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025839 | TAATCCATGACAAAA[C/T]GTTAGCATTTAGAAG | 5521 |
rs143318443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673890 | CATCTTATCTGCACT[C/T]GCAGTTTCCCATTCT | 5521 |
rs143327125 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741480 | TGGAGGGTGAAACAC[C/T]CCCGGTGTCCTTGTA | 5521 |
rs143331855 | in-del | -/AAGT | 0.463989 | 0.129263 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673304 | AGGAAAATTTCTGTA[-/AAGT]AAGTACAAATGTCTA | 5521 |
rs143335114 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661094 | AGCATTCAATCCTCT[A/G]AATCAGTGTTTCTCA | 5521 |
rs143340082 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055881 | AAAGCTGGGGTGCCC[A/G]AGGAATAACTGGAGA | 5521 |
rs143340123 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004682 | ACGAGTTACCCATTT[A/G]TTGTCCCCTGCTTGA | 5521 |
rs143355615 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957095 | TGGGAAGACATGAAT[C/T]ACCAAGTCTTTCTCC | 5521 |
rs143367944 | snp | A/C | 1.6696e-05 | 0.00288924 | intron-variant, missense | PPP2R2B | GRCh38.p7 | 5:147055710 | TGTTCGGAGGTCTGA[A/C]GATGTAAGGCAGGTA | 5521 |
rs143377736 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848062 | ATAGCTGTCCATACT[C/T]CGTCATTTTACCTGC | 5521 |
rs143389648 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904537 | GTTCCCCGAGTCCTA[A/C]AGTATAGCCCAGAGA | 5521 |
rs143393520 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782656 | AGTACTCAATAGTTG[C/T]TTTTTTCCTTGCCCA | 5521 |
rs143394529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933074 | TTAAAGCTGGTTGTA[A/T]TCAACCTTGGAATTG | 5521 |
rs143397768 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019600 | GTTTTGTTTTGTTTT[G/T]TTTTAAAAAGTCTAT | 5521 |
rs143400801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916310 | TTTTTTTTTTTTTGA[C/T]GACTCAGAGGAAGTT | 5521 |
rs143406247 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821872 | TGCCACATTGTAAAT[C/T]CCCATTTATGCAAAG | 5521 |
rs143415213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631449 | TTAACATTCATAAAC[A/G]TCTCTCCACTTGCTC | 5521 |
rs143418083 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862185 | TGGCTTTACCTCATT[A/C]AGAGGGACCTGCAAG | 5521 |
rs143434990 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879459 | TTGGACAAATTATTG[A/C]AGCCTCTCCGTTAGG | 5521 |
rs143454998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653769 | GCTGACATATTCCAT[A/G]ATGTACTACTTAATG | 5521 |
rs143458666 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977561 | CCCTGGTGTGTGATG[G/T]TCCCCTCACTGTGTC | 5521 |
rs143459024 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928622 | TCTTTCACAGGACTA[C/T]TGCAACTGGTTTTAC | 5521 |
rs143465870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623606 | TACAGACATTTTCAA[A/G]TGGCACAAAAAATGT | 5521 |
rs143472302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010663 | CAACTGTAAATACAG[A/T]TGAAGCTTCACTTTG | 5521 |
rs143481319 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838313 | GGCCGGGCTCACACC[C/T]GTAATGCCAGCACTT | 5521 |
rs143481489 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768868 | TAACTATCTTATCGT[C/G]AGGCAAAGATTTGTT | 5521 |
rs143485788 | snp | A/C | 0.000697709 | 0.0186646 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650601 | TCCTCAGGTCATCAG[A/C]GGACATGTAGGTTTC | 5521 |
rs143486421 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620843 | GAACTCCCTGGGGAG[A/C]CTCTGCCCAGGTGGA | 5521 |
rs143497424 | in-del | -/T | 0.0818113 | 0.184966 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071637 | ATTCACAAGACGATA[-/T]TTTTTTTTTTGCCTT | 5521 |
rs143499984 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714665 | GCCAAAATCTGGATA[G/T]TAAGAAAAATGCTAT | 5521 |
rs143502592 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055199 | AGTGAACCAATCCAA[A/C]AATCAACACTCCACA | 5521 |
rs143509525 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637419 | GACAGCCCCTTCCCC[A/G]AAACAAAAATCTATG | 5521 |
rs143527214 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601426 | ACATAGGAAGATTCT[A/C]TTGCTATAAAAAGTT | 5521 |
rs143529055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668299 | TCTAACAGTGTCTTG[C/T]ATAAGGAGGGCAAAG | 5521 |
rs143532961 | snp | A/C | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620653 | TGGGCTCCGGGAACC[A/C]AATGGCAGCATCCCC | 5521 |
rs143551695 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825331 | ACAGTGCAGTGGCCC[A/G]CACTTCCATGTTTAT | 5521 |
rs143557376 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729486 | TAATGTTAATCCCCA[A/T]GACCATGGGGAAAAT | 5521 |
rs143561593 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648472 | CTGTCTACTGGATAG[C/T]GCTACTTTGATGACC | 5521 |
rs143565723 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897062 | AATGATAGTAAAGAA[A/G]CAAAGCAGATACAGC | 5521 |
rs143571126 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825171 | TTTCACAGAGCCGAC[A/G]TTATCACATAGACAC | 5521 |
rs143572731 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867748 | ATATTTTGAGAAGGA[C/T]GGAGTGTCACCTGCC | 5521 |
rs143592384 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719317 | ACACACATAAGCACT[A/G]AATGTTAGTATAGTA | 5521 |
rs143617484 | in-del | -/TT | 0.488057 | 0.0763479 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862764 | TCAAAGAAAAGTAAA[-/TT]TTTTTTTTTTTTTGC | 5521 |
rs143619493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979132 | CTAATAGGACATATA[C/T]GCTTCTACCTGAGTG | 5521 |
rs143621361 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931582 | TTGAGGCATTTCATT[A/G]TTCCTAGCAACTCTA | 5521 |
rs143623439 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147058065 | TAATGAAAGTACAAA[C/T]TCTTGAGGGGGAGAT | 5521 |
rs143629264 | in-del | -/AC | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767540 | AATACACACATACAT[-/AC]ACACACACACACACA | 5521 |
rs143639798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863874 | CGACTCCCAACTGTA[A/T]CCCCCAAAGACTGCT | 5521 |
rs143644129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817264 | ATCTCCTCTTTCCCA[A/T]GGTAAACATTCCCAA | 5521 |
rs143652680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718630 | CATGCATTATAAAAT[A/G]CACACACACCCTTCT | 5521 |
rs143656161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033735 | ACTTAAACTTATCCA[A/G]TTTACTAGCAATCCT | 5521 |
rs143661061 | in-del | -/TTTTG/TTTTTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845315 | TTTTCTTTTTTTTGT[-/TTTTG/TTTTTG]TTTTTTTTGAGATGG | 5521 |
rs143662615 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760122 | ACAGCATGTAACACA[C/G]AGTAAACACGAATAA | 5521 |
rs143669339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826750 | CCTCCCCATTCTTAA[A/G]GATCCAGTTGATATT | 5521 |
rs143671187 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923505 | TAGACCATTGCACCA[C/T]TGGCATTCCTAATAA | 5521 |
rs143680626 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827018 | TAAAGTTAGCACTTA[C/T]ATTTTATTGAAACTG | 5521 |
rs143682345 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990992 | CATCGTTAATCATCA[A/G]GAGAATGCAAATCAA | 5521 |
rs143714909 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935675 | AGGATTGAAAGTAAA[A/G]AGGGCAAGAAAAGAG | 5521 |
rs143719970 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073820 | AGGCAGGCAGATCAC[A/G]AGGTCAAGAGTTTGA | 5521 |
rs143726847 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597321 | GAACCTTGTCATTGC[C/T]ATCCCTGTACCTGTC | 5521 |
rs143737953 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592222 | GATTCATTTTGGATC[A/G]GTGGCAAAGAAAGCC | 5521 |
rs143745866 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987001 | GGGAGGATCCTGAAA[A/G]CAGCAAGAGAAAAGA | 5521 |
rs143749236 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722377 | CTTAACTCAGGTCTG[A/C]GGAGCTACAAAGGCC | 5521 |
rs143755724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810525 | CACAGCCAAACCATA[A/C]CAGATGCGGAAACTC | 5521 |
rs143762753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711921 | CCTTATCAGAACTCA[A/G]GGAAACACATCTCAG | 5521 |
rs143780484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920933 | AAACCTCTTTGGAGA[A/G]AATTAAAATGGAAAA | 5521 |
rs143780884 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994287 | AGAGGTAATAACTTG[C/T]GTAACCCAGCAAATA | 5521 |
rs143803794 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775304 | CACCCTGAGCAAGTG[A/G]AATTTATCCCAGGAT | 5521 |
rs143812429 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938840 | GCATGGAGTGCAGTG[C/G]TGTGATCTCAGCTCA | 5521 |
rs143813877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917797 | AGTCTAATGAACTTA[C/G]AAATGATACATTTTG | 5521 |
rs143819611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981683 | GATACAATAAAGACA[A/G]AGAACATTTCCATCC | 5521 |
rs143829676 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884357 | GAGGAAAATTGATGT[C/T]GTTGTCTGATCCTTT | 5521 |
rs143834155 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847304 | CCTGACATAATAGAC[G/T]TACTTCCTCCTCTTG | 5521 |
rs143835053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697634 | AACCTCACAGAGACA[A/G]CATGTTGAGTTTCCT | 5521 |
rs143837171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670461 | TCAGATTTTCTTATC[G/T]GTTTTATGTGTACTA | 5521 |
rs143848056 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667575 | TACTTAAAAAAAAAA[-/A]CCCAAAAGGATTACT | 5521 |
rs143851787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074862 | TCCTTCCCTCTACAT[A/G]AGTGATCTTTTCAGA | 5521 |
rs143853575 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962398 | GTGTGGTGGCTCATG[C/T]CTGTAATCCTAGCAC | 5521 |
rs143868868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683062 | AGAAATACGGGTGGG[C/T]GTCTTGGCCACACTC | 5521 |
rs143876253 | snp | A/C/G | 0.0103333 | 0.0711729 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958162 | AATCGCAGATCTCCC[A/C/G]AAGGCCCCACCCTTT | 5521 |
rs143877110 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683259 | CAATCTCCTTGAAAA[C/G]TTGTTTTCCAGCCCC | 5521 |
rs143879703 | snp | C/T | 0.0539704 | 0.155153 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912758 | GTGATCCGCTCGCTT[C/T]GGCCTCCCAAAGTGC | 5521 |
rs143893257 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865981 | CCTCTATTAGGTTCC[C/T]GGTACTCTTCTAGAA | 5521 |
rs143898263 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075059 | TATGCTGTAGCTGGG[A/T]TAAAAACAGAAACTG | 5521 |
rs143903691 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695250 | TAACAGTGGTTCTCT[A/C]TGGATGGGAACACTT | 5521 |
rs143903803 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743389 | ACTATCATGCGAGGC[G/T]AAAGGAAGGCATCAT | 5521 |
rs143905891 | in-del | -/TTC | 0.21725 | 0.247846 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670453 | GTACCCCTTCAGATT[-/TTC]TTATCTGTTTTATGT | 5521 |
rs143909264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798129 | GGTGAGTCTGGTTTT[A/G]AGCCTCTAATTGGCT | 5521 |
rs143933252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739729 | TTCTCACATTCCATG[A/G]TCACTATTTATCCAT | 5521 |
rs143951903 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595679 | TTATGTTTTGTTGCA[C/T]AGAAAAAAAGTCTTC | 5521 |
rs143953165 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698587 | AAAATTGTAGCATCT[A/G]TGACTTTCATTGGCC | 5521 |
rs143961230 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852060 | AGCATGAGACCAGAG[C/T]GGAGCTGAAAGAAAA | 5521 |
rs143966399 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637430 | CCCCGAAACAAAAAT[C/T]TATGTAGCGCAAGAT | 5521 |
rs143979652 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919736 | TGGACAGCCCAAACA[A/G]TAGCTCCAGATTCTT | 5521 |
rs144001387 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958833 | TAGCTCTTTGTATGT[A/G]TTAACCAATTTAAAC | 5521 |
rs144008050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038656 | GATACTTTCCCTATG[C/G]TGGTCAAAACTTTAT | 5521 |
rs144009447 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037550 | GCTAACATTCATTTT[G/T]AGAATTTTACATTGG | 5521 |
rs144011746 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838274 | GGATTTCCCAAGGTT[A/G]CAGACTTAGAAGGAA | 5521 |
rs144019866 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752010 | CTGCAGGCCTTGGTT[A/G]GCACTGTGGCTTTTA | 5521 |
rs144025255 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882871 | ACATAGAAAAGGCCA[A/G]TTACAAATACACAGC | 5521 |
rs144026368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809599 | CTAAAACTGGAAGGA[C/T]GAAGCAGCTAGCCTG | 5521 |
rs144029648 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943268 | TTTGGGAATGTGAAT[C/G]GGAAATTTAGTGTGT | 5521 |
rs144055104 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051814 | ATCGCCCAGGCTGGA[C/G]TGCAGTAGTGTGATC | 5521 |
rs144073297 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700773 | CGCTCAACAAGCACC[C/T]ATGGAATTTTGCAGG | 5521 |
rs144100246 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886653 | AAAATCATAAACCAG[A/T]ATAAGCCAACTGCTA | 5521 |
rs144101044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774249 | TATAGGAAGCTATTT[C/T]ACATATAATGCCTGG | 5521 |
rs144103186 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814398 | GAGGCCTCCCCTGCA[A/G]CACACACCAGGAATG | 5521 |
rs144105423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696801 | TGTCATTTTTTTAGA[C/T]TTCTATGCTGGCTTT | 5521 |
rs144115174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710152 | GAAAGCAGCTTACTG[A/G]GATAGAATGCCAACC | 5521 |
rs144118146 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047560 | TCTTAATTTGCACTG[A/G]GTAATACACTATATA | 5521 |
rs144126405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979162 | GCCTTTATACTTGCT[A/G]TTTCCTTGGCCTGAA | 5521 |
rs144139806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660397 | CTGATGTTTATTTTC[C/T]ATAGATATATTTCTC | 5521 |
rs144145187 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975592 | GTCATGCTGTTTTCC[A/G]TAGTGGTTTCACCAC | 5521 |
rs144146530 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918736 | TTTAAATATATTCCC[C/T]TGTAACCACATTTCT | 5521 |
rs144149385 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053366 | ATTGTTGAAGCTCTT[A/T]AATTAGTTCTAGAGT | 5521 |
rs144153203 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716025 | ATCTAATATATTCTT[G/T]TCATTAATTGTGCCT | 5521 |
rs144156338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847902 | AGCTCCTGCGGCTTG[A/G]CTTGGCAGCCTATGT | 5521 |
rs144157403 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669838 | AGGATTCAAATACCA[C/T]CTGAACCTTACAGAG | 5521 |
rs144171439 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656094 | CATATTCTAGGGACC[A/G]GTGCCACAACAGTGA | 5521 |
rs144184776 | in-del | -/AG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890964 | CAGATAGGAAGAAAA[-/AG]AGAGAGAGAGAAAAA | 5521 |
rs144193844 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021349 | GTTTCATGCAGCCAT[A/G]ATTTGGAGGCAGATA | 5521 |
rs144194225 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902577 | ATATACAACTACACA[C/T]GGCCTCGTTAAAGTG | 5521 |
rs144208031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788560 | ACAAGACGAAACCCC[A/G]TCGCTACTGAAAATA | 5521 |
rs144215800 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966708 | ACCTAACACTGGGCC[C/T]GGCACAGCGTAGGAG | 5521 |
rs144224696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711421 | ACTTAAGATGTGAAG[C/T]AAGAAAAAGTTCTCA | 5521 |
rs144237605 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899987 | GAAAATTTCTTCAAC[A/G]TTGGTCCCTAAAAAA | 5521 |
rs144257856 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863075 | GATTTGTAGGTCCTG[G/T]TGGGTGCTTACCAAG | 5521 |
rs144259757 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736821 | CCTAGTGGTATACAT[A/T]TCTGGATCACCTTTG | 5521 |
rs144262065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796127 | CAACAGAAAACACCC[A/T]TATAAAAATGTCATT | 5521 |
rs144275871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935167 | GCAAGGTGATGATAT[A/T]ACGAACTGGGGCCTT | 5521 |
rs144279128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009444 | ATTTCTTTGAAAGCA[C/G]ATAATCTAAATCCTC | 5521 |
rs144280757 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908552 | TTTTGGCATAGGGGT[A/G]TGTTAAACAATTACT | 5521 |
rs144287952 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947701 | TAGACTTTCTGTGAG[A/C]GATCTAACGGCCATA | 5521 |
rs144297178 | microsatellite | (CA)12/18/19/20/21 | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667333 | ATAGGCGTGCGCGCG[(CA)12/18/19/20/21]AAGGAGATAAAAAGT | 5521 |
rs144301234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070303 | TATTCTTACCTGCAA[C/G]CAAATTGGTATAAAG | 5521 |
rs144305448 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017455 | GTTATCATTAGAAAA[C/G]AGAGTGGTTCAAACC | 5521 |
rs144310592 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974890 | GACACGGGGTTTCAC[A/C]ATGTTAGCCAGGATG | 5521 |
rs144312027 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056943 | ATTCAGAGGCACAAG[C/G]AAATGATTTAAATGT | 5521 |
rs144313831 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066689 | GACAAATAAGAAAGA[A/T]ATGGCCCCTGTCTTA | 5521 |
rs144321347 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898128 | AAGCGGAGGTTGCAG[C/T]GAACTGAGATTGCAT | 5521 |
rs144332623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689072 | AACTGAATTGTCTCA[C/T]ATATATAGGCCCACT | 5521 |
rs144336456 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604539 | GTCTTGGTGAGAAAC[A/C]TGATAGCCCAGTCCT | 5521 |
rs144339614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731675 | TCTGTAAAACAGTGA[A/G]GAAAATCTTTCCACT | 5521 |
rs144346135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146622546 | CAAATACCTATAACC[A/G]GCCTTTATAATTTAT | 5521 |
rs144350472 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672713 | TCCCTCCCTCTATAA[A/G]TAGTATATGCAGCTG | 5521 |
rs144357790 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684665 | ACCCTCCAGATGCAT[C/T]GTGGAAACTCCTTCC | 5521 |
rs144357921 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801598 | GATGGGAAGATACAG[G/T]CTGTGGGGTCAGGCC | 5521 |
rs144372772 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076617 | TTGTCTTAAAATGGT[C/T]TCTTCCCACAAGTCT | 5521 |
rs144376222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633922 | TCTACTTGTACCAGC[A/G]CATGCCTCTCTTTTA | 5521 |
rs144389408 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906612 | CAGGCGTGAGCCACC[A/G]CACCTGGCCTTTTTC | 5521 |
rs144394093 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837639 | CAAACTCAAGATATC[A/G]AAAATACCATTTCCA | 5521 |
rs144403311 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867004 | TTACTGAGAGTCATT[G/T]GTGTTTGTTTCCAAA | 5521 |
rs144409361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753635 | TTCGGTCTGATGCTC[A/G]GTTTTAAACTAAAGA | 5521 |
rs144409450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799017 | ATACACTGAATACTC[C/T]GAGGTGACTTTTTAA | 5521 |
rs144421121 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034803 | AGTTTTGGAATGTTT[C/T]CATTAGTTTCTCAAG | 5521 |
rs144422404 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681062 | TATTTAAAATGCTTA[C/T]ATCAATGCATCAGTC | 5521 |
rs144424961 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924935 | TTCTTTATCCAGTCT[A/G]TCACTGATGGGCATT | 5521 |
rs144434693 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720486 | CTTGGTTAATCTAAA[A/G]TATATCATATGGACC | 5521 |
rs144438853 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642271 | ACCAGGAGGTCACTC[C/T]TTAAGGGATCCACTT | 5521 |
rs144449790 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022168 | AACAGAACATAAGTG[C/T]TGTGTAGGAAACTAT | 5521 |
rs144459681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944779 | CAACCTTTAAAACAA[C/T]TTATTAAAGGTAAAG | 5521 |
rs144464401 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828947 | TTATTCAAGGAAAAA[G/T]AAACTTTGATACAGG | 5521 |
rs144466416 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762184 | AAAGAAAAAAGTTAC[C/T]GATATTGGCTAAAAC | 5521 |
rs144470213 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910289 | TTGAAGGCTATACAG[C/T]TATGGATGCAAAAGC | 5521 |
rs144487822 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839859 | GTCACCATTTCTACA[A/G]TTTTATTCATCCTTC | 5521 |
rs144488722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642634 | TCTGAAAATGATGAG[C/T]TAAATGGGAAGACAC | 5521 |
rs144489693 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680414 | GTGGGGTGGGGAGGG[A/T]GGGATAGCATTGGGA | 5521 |
rs144489874 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799716 | ATAGCTCTCTGCTAA[C/T]GACTATGATTGTAAT | 5521 |
rs144505210 | snp | C/T | 0.00468089 | 0.0481512 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147035190 | GCATGGCTGGGGAGG[C/T]CTCAGGAAACTTACA | 5521 |
rs144508065 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819490 | GAATGTGGAGATGGC[A/G]AAGTGTCAACTCCTG | 5521 |
rs144509411 | in-del | -/ATATACATAACAAACATTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840227 | ATTGAGTTCCCTTGA[-/ATATACATAACAAACATTT]AATTGAGTGACTCCT | 5521 |
rs144512231 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594819 | AGTGAGGCTGAGAGA[C/G]AAGGAGATAGAACTG | 5521 |
rs144516115 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080763 | TGTCTGGACTCAGAA[C/T]TCTACAGCGCTGACA | 5521 |
rs144533485 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996476 | AAATGGAACAACTTC[A/T]GCACCACACTGAGAA | 5521 |
rs144534027 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948183 | TAAGACTGGGGACTA[C/T]GTTTATTCAACATTC | 5521 |
rs144535633 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790815 | CCACATTCCATTTAG[C/T]ATTGAAGAGAGGAGG | 5521 |
rs144541705 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713462 | TAAAGCTTATGTTAC[A/G]TACATTTTACAACAA | 5521 |
rs144555444 | snp | C/T | 0.000186895 | 0.00966502 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638426 | AATATCTGGCACAGA[C/T]GAGTCAAGGAAGGAA | 5521 |
rs144557260 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689056 | GTATAAAAAGAAAAA[C/T]AACTGAATTGTCTCA | 5521 |
rs144578236 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844580 | AGATAGGGCAGAAGA[C/T]CTGCATGCCCGGATC | 5521 |
rs144578373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777699 | TATTTGTAATGGCAC[C/T]ATACTATGACATATA | 5521 |
rs144578666 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648056 | GACTAGCTAGCTGTG[C/T]ACCAAAACCGGGTCT | 5521 |
rs144590920 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841326 | AAAGGTCATTGGTTT[C/T]TATATCTTTGTAGAG | 5521 |
rs144598670 | in-del | -/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985018 | TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCAC | 5521 |
rs144604744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649128 | ATGCTAGTGTAGGTA[A/G]GTAGATAGGGATATA | 5521 |
rs144607914 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769172 | CCAGGCAAAGCTTTT[A/G]TAACCACCTAAAGCA | 5521 |
rs144615667 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771740 | TTTTCTATTTTTCTT[C/T]GGTATATAGCTAATC | 5521 |
rs144623186 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953637 | CACCAAGTGAAGAAG[A/T]TAATATGGCAAAATG | 5521 |
rs144631150 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838624 | AGAATGGGACAGAGT[A/T]ACATAATGGGAAGGA | 5521 |
rs144634596 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767782 | TAGGGTTCACTCTTC[A/G/T]CATTGCACATTCCAG | 5521 |
rs144635783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671963 | AACGATAAGCAAAAC[A/G]GAGAGAATAAAGGGA | 5521 |
rs144649302 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050866 | CAGCAAACATGCTTC[C/T]GGGTGTCACTGGAAG | 5521 |
rs144650168 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065873 | GTGCCTGCTGGGTGC[A/G]GGTCCGTGAGCTAAA | 5521 |
rs144680052 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695469 | TATTTTTTATTGAAA[C/T]TGTAAGTTTGAAAAT | 5521 |
rs144699291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600098 | GTCCATATCAATTAA[A/G]TTGAATTCTAGCCTC | 5521 |
rs144700434 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734471 | GAGGAAACTGAGGCA[A/C]AGACTGGTTACTTAT | 5521 |
rs144703684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605404 | TTCCATTTCCCTTTC[C/T]TAATCCCCACTACTC | 5521 |
rs144709761 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998756 | CAGAAATAGATTAAA[A/G]TGACTTTATTCCACT | 5521 |
rs144710980 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653529 | GTACCAGAGCTCAAA[C/G]CAGGACCCCAAGGGT | 5521 |
rs144717968 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048360 | TACTCAGCCTTTCTG[C/T]GTCTTATCTGCTCAC | 5521 |
rs144718241 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046311 | GATCCAGAGCAGGCT[C/T]TCATACATATCTTCG | 5521 |
rs144721052 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974113 | GATCTATTTGGAATC[C/T]GGGCAAGAAAGTATC | 5521 |
rs144721119 | snp | C/T | 0.472241 | 0.114494 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013238 | GGAAATAAAAGAGGA[C/T]ACAAACAAATGGAAG | 5521 |
rs144723448 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045206 | TCTCTGTTTTGTGTG[C/T]CCCACCCCTTAAAAT | 5521 |
rs144729348 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875712 | ACAGAAAAGCAAGAT[A/C]TATGGAAGGACTAGA | 5521 |
rs144736637 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617435 | CCAATGTGATTATTA[C/T]TCATTGCATGTGTGA | 5521 |
rs144738574 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986456 | CTGAATAAATTGCAG[A/C/T]GGAAGGCAAATTGGA | 5521 |
rs144747571 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704510 | ACTTGAGCATTTTTC[C/T]TCTGTTGTATATAGA | 5521 |
rs144758034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732927 | CTGATTCTAAAGCCC[A/G]TCTTCTGCTATTGCT | 5521 |
rs144766793 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930426 | TGGGTCTTTATTTGT[A/G]GGATGACTTTTCAAT | 5521 |
rs144768707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651167 | CTTTTCATCTCATGG[C/T]TTTGGAAGCTATACC | 5521 |
rs144781279 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646739 | AATAAAAGCTACCAT[G/T]CTAATGTTCAACTTT | 5521 |
rs144789294 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692812 | GTGCTGGGATTACAG[A/G]CGGGAGCCACCACAC | 5521 |
rs144795367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052111 | CTGCACTATTTGGTT[A/G]CCCTGGCTTCTGTTT | 5521 |
rs144800168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607909 | GCAGCATAGACAATA[C/T]GTAAACAGATGAGCA | 5521 |
rs144803171 | snp | A/C/G | 0.00478244 | 0.0486902 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892737 | AGTTTGAAAAAAAGC[A/C/G]TCATGCTATAGCCCT | 5521 |
rs144806484 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930117 | TTATGAAGAAAATAA[A/G]TCAGGGTTATGTGAT | 5521 |
rs144812057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766739 | TACCACAACACCGTG[A/G]GCCCTACGGCACCAT | 5521 |
rs144814849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872028 | GTGTCGAAATTGGAC[C/T]CCTATTTCTTCTTAA | 5521 |
rs144816647 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927836 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTAC | 5521 |
rs144830349 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046754 | ACTATTTTTACCTGT[A/G]AAATGTGGATAATAC | 5521 |
rs144838740 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842441 | AATTCAAGAAAAAGG[-/A]AAAAAAAAAAGACAT | 5521 |
rs144842938 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896779 | TCCAAGATTTAAAGG[A/C/T]GTTAGTGGGGGTTGT | 5521 |
rs144858663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001680 | GTGGTGAGTACCATC[A/G]GACCCCTTTCGTTTG | 5521 |
rs144871785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926413 | TTTTTTTTTGTTTTC[A/G]AGACGGAGTCTTGCT | 5521 |
rs144883045 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007175 | TAAAGAGTTCCCATC[C/T]GGAGGACACTACAAC | 5521 |
rs144896396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894801 | TTCATTCTCCTCCTC[A/C]CTCTGCTAATTCATG | 5521 |
rs144898161 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822480 | GCTCCAGGGCCTTTG[C/T]ATTTACTATTTTCTC | 5521 |
rs144925031 | in-del | -/TTC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796458 | TACAAATGGCAAACA[-/TTC]TTCTTCTTTTAATTT | 5521 |
rs144932556 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669768 | TTTAAAGAGCTGAGG[C/G]TCAGTGAGGTTAAAT | 5521 |
rs144946436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840808 | CTGCTCATTCTAAAA[C/T]AATCTATTCATTGTC | 5521 |
rs144969721 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949561 | AAGCCTCTTATGCTG[C/T]TGGTGGGGATGTAAA | 5521 |
rs144971382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824531 | AGGGTTGGCCATACA[C/T]AGAATAGTTGAGTTT | 5521 |
rs144971841 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028267 | TTGATCCTGCAGGAC[A/C]AAGGCTAATAATAAT | 5521 |
rs144975394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755779 | GTGCTAATTTGTTTT[C/T]CAACTTCGAGCCTGG | 5521 |
rs144979342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709864 | TAAGTTTTCTGTTAT[A/G]TTCATCTAAATTCAT | 5521 |
rs144980673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753276 | GTGTCTGGTACACAA[A/G]AAGTGCAAAATACTT | 5521 |
rs144986554 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630034 | GGCCAGGCTGGTCTC[A/G]AACCTCCTGGCCTCA | 5521 |
rs144988215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690199 | GCTGTTGGGGCTAGG[A/G]CTATCCCAACATGTG | 5521 |
rs144989656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751578 | TTCAAGAACTGTTGA[C/T]TGAATAGAAATAAAT | 5521 |
rs145004335 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623961 | GCTTGAATTAACCGA[C/T]ATACTTAAACATGAG | 5521 |
rs145013423 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010859 | AACCTACTCTACAGC[G/T]GCCACCCTGGACTGA | 5521 |
rs145017907 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591458 | TGCCTCCATGATCTC[A/G]TTTCAACTTCTATTA | 5521 |
rs145024420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803123 | GTTTATTCCATAGAG[C/T]GCATGCCTAATGCCA | 5521 |
rs145026494 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733969 | GGTAGTAATAACAGC[A/T]AACATTTATTGAGCA | 5521 |
rs145029657 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819557 | AATTCCAGAAAATGT[A/G]CTATTTAAAAACTAG | 5521 |
rs145047764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750548 | GTAGATTGGATACAG[A/G]ATATTTCTGTACTGT | 5521 |
rs145052426 | in-del | -/AA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821788 | GCCTAGTACTCTGCC[-/AA]AAAAAAAAAAAGCTT | 5521 |
rs145058972 | snp | A/G | 0.122064 | 0.214785 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846507 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 5521 |
rs145075065 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635815 | AAATATTTCCTGACC[C/T]CTGCTTATGTGTCAG | 5521 |
rs145085953 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906472 | GGATTACAGGCATGC[A/G]CCACCACGCCCAGCT | 5521 |
rs145090614 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986100 | CTGATTTTACCATAA[A/T]AACAAGAAGAGGCAC | 5521 |
rs145095401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068251 | CTCCTGACAAGCCTA[C/T]GAAGGAGAAACTACT | 5521 |
rs145119525 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980710 | TGTTATATTGATTTA[C/T]AGTATCTTTTGCATG | 5521 |
rs145121899 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639055 | CTTATCCTCATTTTT[C/T]CAGGGGTGGAAACGG | 5521 |
rs145131892 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022766 | ATTACCATTGACGTC[A/G]CATCATAAACAGAGC | 5521 |
rs145157780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946129 | TGTGTTCCCTTTTAA[C/T]GCTGTAGCCGCTTAA | 5521 |
rs145165255 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989443 | GCAAGGATGGTTCAA[C/T]ATATGAAAATCAATA | 5521 |
rs145175275 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875289 | TTAACTTTAAAAGAG[A/G]AGGAAAGGTAGGGGA | 5521 |
rs145181926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644115 | TATTGCTAAAGTAAT[A/T]TACCAAAAAATAACT | 5521 |
rs145196776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655187 | CTGCTTTCAAAGGAC[A/G]CACATCCCAGCACTG | 5521 |
rs145207453 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049442 | CATCTGATTGGAAAG[G/T]TTGGCTAGGAAGTTG | 5521 |
rs145211835 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874048 | ATTCATCCTTTAGTT[C/G]TCAGTTTCAGCTGTC | 5521 |
rs145217449 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762954 | CACTTTGAGTTCTCT[A/T]GTTGAGCCTCTGTCA | 5521 |
rs145220464 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807195 | TGGTCTTCAAGATCT[C/T]TTCCAGATTTTTCAT | 5521 |
rs145226940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803084 | CTTCATATGCTCCAA[A/G]TGCTACTTCTCTCTC | 5521 |
rs145232592 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596510 | CTTTAAATTACTTCA[C/T]GTAAAAGCTAGCTGG | 5521 |
rs145237288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690972 | CCTTTCCTGCTTCTC[C/T]ATCTGCCACCAGAGA | 5521 |
rs145250721 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893405 | TGCCTTTTGAGTGGT[A/G]CCCACCATCGACCTA | 5521 |
rs145251473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734871 | ATTGCAGATTTTGAT[A/G]GCAAAAGCTACAATT | 5521 |
rs145258988 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983624 | CCTTTACACTAGTTT[A/G]TTGTCCCCCATTTAT | 5521 |
rs145268997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146910878 | ATATCTTCTAAAGCT[C/T]TCCCTGAATATCCCA | 5521 |
rs145278050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877187 | AGGCAGAATGAGATT[A/C]CACCTGCTGACTTTC | 5521 |
rs145279503 | snp | G/T | 0.000561454 | 0.0167455 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698019 | TGCATTCTGCTGGGG[G/T]AGCCATCTTATTTTA | 5521 |
rs145284116 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756955 | GTGGAGGAGGCAGAC[-/A]AAATTAAGATTAAGG | 5521 |
rs145292022 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803842 | CAGTGCTTGCTTCAT[A/G]TAGTTGTTGTGAGGA | 5521 |
rs145329010 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718108 | CATAATTCACAGGAA[A/G]CACAGCTGATTTTTT | 5521 |
rs145330345 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606835 | CCTGGCTGTGATGAC[A/G]CGGGCAGATGAGAGT | 5521 |
rs145337450 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080771 | CTCAGAATTCTACAG[C/T]GCTGACAGATCATCC | 5521 |
rs145348770 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805669 | GTAGTACAAATTGCA[A/C]CCTAGGAAAAAAATG | 5521 |
rs145358118 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802817 | ATCAAGCCTTTAACT[G/T]GTGCCCCAAGGCTCA | 5521 |
rs145364109 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733266 | CAAAGTACAGGGCTG[G/T]GTGGTCAAAAAACAG | 5521 |
rs145371750 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826656 | ATGCATTCTGGTGGC[A/G/T]TTTTCAAAACTCAGC | 5521 |
rs145408779 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889547 | AGGAGGTTAATGGCA[C/G]GGGGGTAATGCATGA | 5521 |
rs145420810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791613 | CACTCACTCCTCAAA[A/G]CTCTCCAAACATGTC | 5521 |
rs145427939 | snp | A/C/G/T | 0.004783 | 0.0487016 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067772 | TCTAAGTGTTTAATC[A/C/G/T]CACAGTTACCTATTT | 5521 |
rs145452412 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002056 | CTTGCCTCCTGGGTC[C/T]TAATGCCTGTCAAAC | 5521 |
rs145488586 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964032 | TCTCCAGGCATGTAG[C/G]CCATCCAAATGTAGC | 5521 |
rs145492013 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782851 | AAAGAAGAGAGGAGA[C/G]ACAGAGAGAAACAGA | 5521 |
rs145493197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707518 | GATGCAGACACCAGG[C/T]CCACTCGTGTAGGAG | 5521 |
rs145508342 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879204 | AGCTTCAGAAAAAGA[A/G]GAGAAAGTGGGAAGT | 5521 |
rs145510695 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806706 | TTGCTGCAGCTTAAC[G/T]AGCAGTCACCAACCA | 5521 |
rs145517204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860058 | GAAAACAATTTTTCT[A/C]GTGATTTTACCTTTA | 5521 |
rs145517533 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915178 | CCTCACTGGTTTTCT[C/T]ACATCTAATTTTGCC | 5521 |
rs145538173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988662 | GCCTACATCAAAATA[G/T]TAAAAAGATCTGAAA | 5521 |
rs145540686 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854054 | ACCAGGTCTATATAC[C/T]AAACCTTTGCATCCC | 5521 |
rs145565394 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661473 | AAATATATAAAATAT[C/T]TATGTTTAATATCTA | 5521 |
rs145573029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050484 | CATAAATATGAAAAA[A/G]GTACAAAATATAGTA | 5521 |
rs145574482 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976961 | TGGATATTTCTCTCT[A/C]TATATGTTTCTCCTG | 5521 |
rs145575536 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054506 | AAAGTCCATGAGATA[C/T]CAATGTCTATGAAAA | 5521 |
rs145581075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923841 | CCCATCAGTGATAGA[A/C]TGGATAAAGAAAATA | 5521 |
rs145582559 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768410 | GCTTCCCAAGAAATT[C/T]CTGGGGGTGAAATGG | 5521 |
rs145582932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969035 | AGCGGGTATTTGTCA[A/G]CTCCAGCCTACCACT | 5521 |
rs145585997 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962737 | TTTCAGAATTACAAG[C/T]ATAACCTTATTTGAT | 5521 |
rs145590207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044846 | TATATCTTGCTGAAT[A/G]AACATGATATGAAAA | 5521 |
rs145606297 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939996 | GAATATTTACATAGT[A/G]TCTATCTACCTACAC | 5521 |
rs145612551 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925597 | CATACAACAGTTTGA[A/C]AATGATGTGTTCAAG | 5521 |
rs145613431 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873672 | ACTGGAGTGCGGTGT[C/T]GCGACCTCGGCTCAC | 5521 |
rs145622818 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857929 | CGACCTCAGGTGATC[C/T]GCCTGCCTTTGGCCT | 5521 |
rs145627690 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698010 | AAAGTAAGCTGCATT[C/T]TGCTGGGGGAGCCAT | 5521 |
rs145629654 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792471 | GAACAAAACAAACAA[A/G]TGTCCTTTTGGAACA | 5521 |
rs145633155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816645 | ATGAAGACTGCATTG[C/T]CCAAAAATTACTTCA | 5521 |
rs145633691 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748545 | TCTGTTCTCCATTTC[C/T]ACAACATTCTTGAAA | 5521 |
rs145634604 | in-del | -/TTTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670484 | TGTACTATTATTTAT[-/TTTA]TTATTTATTTATTTA | 5521 |
rs145635767 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671427 | AGCTGGGATTCCTGT[C/G]TGGACACTGAAGGCC | 5521 |
rs145640738 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790260 | CTCATTTCTGTGGAA[A/G]GGAACTGGGAGAGGA | 5521 |
rs145676172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751289 | TCACAGAACATAGCG[A/G]GGAAGAGGTCATAGA | 5521 |
rs145679571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965888 | AGGCAAAGTGTTACT[C/T]GCTGATCCTCAGATC | 5521 |
rs145679608 | snp | A/G | | | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923140 | TTTTTTTGTTTAGCC[A/G]GTTTTGAGCCAGATT | 5521 |
rs145680065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072677 | AAGGAGTCTGATCTC[A/G]TAAAACCTGATTAAA | 5521 |
rs145698583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685564 | ACTTGCCTAATCTCA[C/T]GACCTTTTAGCAATG | 5521 |
rs145714056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620499 | CTCGACAGGAGCCTA[A/G]TGAAGAAATCTGGTA | 5521 |
rs145720042 | in-del | -/TCTC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675821 | CCAACCTCAGTCACT[-/TCTC]TCTCTCTCTCTCTGG | 5521 |
rs145724948 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867821 | TACTTCACCATATGC[C/T]CCAGAACTTCCTACA | 5521 |
rs145726167 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799389 | AGAGTCCAAGGTCAG[G/T]AAAAGAGGTGTGAAA | 5521 |
rs145730245 | in-del | -/GTTTT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861856 | TTAAAATACAGCATT[-/GTTTT]TTTTTTTTTTTGGCT | 5521 |
rs145735824 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069232 | AGACAGCATTTTACT[A/G]TGAGAGGTGAGGTAT | 5521 |
rs145736914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062600 | CAGTACAGGCTTTCC[A/G]CTTATTCCTTCCCTC | 5521 |
rs145744587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639297 | AAAGTTTTAGGGTCC[C/T]GTGGAAAATATCCTT | 5521 |
rs145747835 | in-del | -/CTTC | 0.261332 | 0.249743 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900555 | CTTTTTCCTTCCTTT[-/CTTC]CTTCCTTCCTTCCTT | 5521 |
rs145754015 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635474 | AGTTCATCAAGCTTC[C/G]CAGTCAGTTGATTCC | 5521 |
rs145760232 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023721 | ACATTATTTCTGAGT[A/G]TGTCTGCAAGGGTGT | 5521 |
rs145761992 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854535 | ACCTTTTATCTAACC[A/G]TATATTTGTACCCAT | 5521 |
rs145771285 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759869 | CATTTGTCAACTCCA[C/G]TGCTTTAGTTGTTGT | 5521 |
rs145790049 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664500 | AGACCCATCTTCAGG[C/T]TCCATTTTTAGTTCT | 5521 |
rs145790384 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960339 | CTGTCACCCAGGCTG[A/G]AGTGCAGTGGCACAA | 5521 |
rs145801977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753573 | TGATATTACAGGGAG[A/G]GAGATTCTTGCCAGC | 5521 |
rs145804131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933170 | CTGAGATTTCAAGTA[A/T]CAGGGATTGGAAAAT | 5521 |
rs145818778 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632254 | AAGGCAGTGTAAAGA[C/T]ACAGGGAGAAGACAG | 5521 |
rs145824897 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940868 | TAGTTACTCTAAAGA[C/G]AATATGAGTGATTTC | 5521 |
rs145826697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900779 | TTTTCCTAATGCCCC[C/T]CTCTCCCCGTGCCCC | 5521 |
rs145826912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828175 | CCATCCATAATGCAC[A/G]TTCTCTAGTTGAAGG | 5521 |
rs145831108 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947122 | AGGGAAAAATTCCAT[A/C]ATATGAGGCAGATGC | 5521 |
rs145845142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711427 | GATGTGAAGCAAGAA[A/T]AAGTTCTCATTTGGA | 5521 |
rs145856742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911850 | ATATACAATGAATAA[A/G]GGTACACTTCCTATA | 5521 |
rs145856954 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842126 | TCCCCTTAAAGTACT[A/G]CACATTTATCTTCAG | 5521 |
rs145865733 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810113 | TTGCAAGCCTGACAA[A/T]TAGCCTTGTGAAAGT | 5521 |
rs145873717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823102 | CTCCAGTTTGGAGCT[C/T]AGCCCCCTGTTCTGG | 5521 |
rs145879857 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023490 | ATACTGCCTAAAAAT[A/G]TACACTTTAAATATA | 5521 |
rs145888274 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920467 | AAAGGAAATTGTACC[A/G]TTCTAAGAGTCATTA | 5521 |
rs145892149 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936619 | AGAACCTCTCTGTAC[A/G]GAGAGATAGTAAGAG | 5521 |
rs145900995 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030741 | CCGAAAGTCTAAGAG[A/C]GCTTAATAACTTTAA | 5521 |
rs145905762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839036 | AAAATTCGTCCACAT[A/G]CTGATTTCCAACCTT | 5521 |
rs145906943 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951901 | TTGCTGGGTCAAATG[A/G]TGTTTCTGGTTCTAA | 5521 |
rs145924637 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797488 | CAGGAGGATGATAAC[A/G]CCCATCTTTCTGGCC | 5521 |
rs145925076 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042103 | TAACGCCCAAATCCC[C/T]ACGTCTATCACCTTG | 5521 |
rs145934120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725588 | TATCGATTTTTAGTG[C/T]ACTATCCTCTTCTCA | 5521 |
rs145939787 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598480 | CATACTTGTGAGTGT[C/T]AGATTTATATCTTGA | 5521 |
rs145941384 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727368 | TACATATTTATGGGG[C/T]ACAATGTGATATTTC | 5521 |
rs145944893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038672 | TGGTCAAAACTTTAT[A/G]TTCATTATCCCAGTT | 5521 |
rs145955979 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814411 | CAACACACACCAGGA[A/G]TGTCAGGAGACCATC | 5521 |
rs145965502 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886965 | ACATATAAAAACATA[G/T]ATGTGACCAGAATGT | 5521 |
rs145973433 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922594 | TAGTCAATGTTTCCT[A/T]ATGGTGGGATAATAG | 5521 |
rs145980429 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602304 | TTTGGTCTTATTTTC[A/G]TATTCAGAGTCTTAC | 5521 |
rs145982009 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996583 | TTCTCATGGCTGTAT[A/G]GAAGAATGATTTCAG | 5521 |
rs145994054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782189 | AGGCTGCAGAACTGT[A/G]AGCCAGTTAAACCTC | 5521 |
rs145994151 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821066 | CAGCCACACCCTGGC[G/T]TCTCACCAGGTCACT | 5521 |
rs145995523 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706271 | ATCTTCTTCACAACC[A/G]TGGCCCTGGTGGAGC | 5521 |
rs146007468 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891078 | TCGTAGAGAATAAAA[G/T]TGGCTGTCACAGATA | 5521 |
rs146011979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818182 | ATTTGATCAAAGTAC[A/G]TCTTTCCCGCCAAAT | 5521 |
rs146020054 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786594 | CCCTCTGCTTTCTCC[A/G]AGCTCTTAATTTATA | 5521 |
rs146023347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660786 | TTCAGGTCATTAAAT[A/G]TCTTAGAATTATATT | 5521 |
rs146024041 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812980 | AGCTACAATTCAAGA[A/T]GAGATTTGGGTGGGG | 5521 |
rs146045243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633240 | AATGCAGCTCTGATA[A/G]CACGGTTCTCCTCGG | 5521 |
rs146046188 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020663 | GGTTTTGATAGAGAT[G/T]GACAGAGAAGGTATA | 5521 |
rs146047296 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903595 | TTGAGATGGGGTTTC[A/G]CCATGTTGCCTGGAC | 5521 |
rs146047496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793683 | TCTAGAGTCTGTGTT[C/T]CTGTCACCCAATATT | 5521 |
rs146048973 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014399 | gggtatatacccaaa[G/T]gactataaatcatgc | 5521 |
rs146061258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705548 | TCATTAAACAAACGG[C/G]ATTCTTAGGTGTCCT | 5521 |
rs146064648 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626947 | AACTGGTTAAATTAA[A/T]CAAAAATGGAAATGA | 5521 |
rs146085248 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981955 | GCAGTTGGCCCAGGT[C/G]GTCAGCATTTGGTCA | 5521 |
rs146091001 | snp | C/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867387 | ATCGGGCCTTTCATT[C/G]AAATTAGTAAATTTA | 5521 |
rs146104574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979013 | TCCAATAGTTCTCCA[C/T]TTCACCTGGAGGAAA | 5521 |
rs146105782 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601007 | CTTTCTGATTCTCAT[C/T]CTGGAAATTTCACAT | 5521 |
rs146114415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762494 | CTTTCTATTCAAGGT[A/G]CTGTGCTAAGATTTT | 5521 |
rs146115785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995849 | CCTGACTTCTTAGAG[A/G]TAGCAGGAATAATTT | 5521 |
rs146116498 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078227 | TAGCTTACAAATATC[G/T]AGTACTTACAAAGTA | 5521 |
rs146134401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872503 | CAATGCCTTCCCAGC[A/G]TCTTCATATCAAAAG | 5521 |
rs146141833 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835470 | TGAGTTCTAGCAAAC[A/G]TGTACATCTTTGGTT | 5521 |
rs146142073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766446 | AGGAGTGAGTGGGGA[A/G]TGGGAAAAGGCTCCA | 5521 |
rs146143537 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721842 | TGCAGGATAGGTAGG[C/T]ACTGCTCTCCCATTC | 5521 |
rs146161158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642765 | TATTTCAGGCTGGAA[A/T]AAATCTTAGGGCCAC | 5521 |
rs146169602 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608402 | TGGATTGTCTTTGTC[A/T]GTTTTCCTTATCTTG | 5521 |
rs146185567 | snp | C/G | 0.00954224 | 0.0684493 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687503 | AAGTGCTAGATACCC[C/G]CATTTTCACCTGCTA | 5521 |
rs146187362 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604040 | AAAGTATTTCGATAC[A/G]TGCCAGGCCCTGTAC | 5521 |
rs146212043 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919384 | GCACCCTGGGCCTGA[A/T]GGTTTACCTCCCCAA | 5521 |
rs146212194 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848341 | GTCCATAGTTCATTC[A/C]GATTTGCTTAATTTT | 5521 |
rs146219052 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728885 | CTCTTTTTATTTCCA[G/T]TCTCAGGTATGTCTT | 5521 |
rs146227548 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038512 | AAAGTTCTTGGGAAA[C/T]TATTTTCTACTTTAT | 5521 |
rs146236631 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744556 | TGAAATTCCACTCCT[A/G]CCCTCACATGTGTCA | 5521 |
rs146243138 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597632 | AGAAACATAAAATCA[A/C/T]ACAGGTTAATTTCCC | 5521 |
rs146252478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922354 | AAAATAAACACCTCT[C/G]CAGGACTCTCCCTCC | 5521 |
rs146252607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851142 | CTCATGCAGTAAAGG[C/T]TCACAATGGTGCCAA | 5521 |
rs146260967 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817780 | ACTTTACATCTCTCA[A/T]CTAGGCTCAGTTTCA | 5521 |
rs146262099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748861 | TACAGGTTTGTATAT[A/G]GGTTTTTGTGTGCAC | 5521 |
rs146262404 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700670 | TAAACTATGTTTTTT[A/T]CCTCCTGCATATTCT | 5521 |
rs146267604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015873 | TTTTCTCAATAAATG[A/G]TATCTATTTTCAGTA | 5521 |
rs146272762 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764819 | AGAGAGAGAGAGAGA[G/T]AGAGAGAGATACACG | 5521 |
rs146289361 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064895 | GAAATACCAGTTTGG[G/T]CAGTAGAATGAATTT | 5521 |
rs146302995 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990835 | TTATTATTCAGAATA[C/T]ATAAGAAACTCAATG | 5521 |
rs146305068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040162 | TAAATGAACATTGGG[C/T]ATCACTGGAAGCCTC | 5521 |
rs146305667 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668123 | CTCATCTCATTCCTC[C/T]TTTCTTATATGTACC | 5521 |
rs146306147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058233 | TACTTTTTATGTGGA[C/G]GTGAAGGTCCTTTAC | 5521 |
rs146318955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830980 | GCAGCCATCATAATG[C/T]CAGAGTGCAATGCAT | 5521 |
rs146326071 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019895 | CACCGCTCAGATCTC[A/G]TTTCAAGGAAAACAT | 5521 |
rs146332112 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902260 | TTCCTGAGTCCCTAT[A/G]GTAGTCAAACAGCAA | 5521 |
rs146332113 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943545 | ACTCCATTTTAATGT[G/T]TTTTCTTTAAATTGC | 5521 |
rs146335659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939424 | GGGTGATGAGCAGAA[A/G]TCAAGCTTAGGCTTC | 5521 |
rs146344566 | snp | A/C | 0.0839998 | 0.186933 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014761 | AGGGGGGAGGGATAT[A/C]ATTGGGAGATATACC | 5521 |
rs146359171 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727922 | TTTTACTTTATACTT[C/T]TATGAGTTTGACTTT | 5521 |
rs146374772 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904781 | TCAAAATGAGGGCAC[A/G]GACATGGTACTGGAG | 5521 |
rs146381546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801068 | TATGCAAAGTGAAAT[A/G]AGTCAGATGCAGAAT | 5521 |
rs146384837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684394 | CCAGAATGAGTATTA[C/T]GACATAGGTACCTCA | 5521 |
rs146385089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730959 | GAAGAAACCGATGAG[A/G]CCTTCGAGGCTCACA | 5521 |
rs146405747 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644568 | GAACCTCATCTCGAT[A/G]GGTAAAGTTTGAGAT | 5521 |
rs146411455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919749 | CAATAGCTCCAGATT[C/T]TTGCTATGTAGTTGA | 5521 |
rs146421861 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979559 | TCTTCCCACCTTGAA[-/AC]ACACACACACACACA | 5521 |
rs146428129 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988975 | ACTACTATGAACAAC[C/T]ACACGTAAATAAATT | 5521 |
rs146440696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774333 | CACTATCAGCAATGT[A/G]TTTTTGTCTTAAACT | 5521 |
rs146442539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696889 | GATTAATATGAGACT[C/G]ATTGTAAAACTTTAC | 5521 |
rs146457450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883051 | CTGTCCAATTAGCAC[A/G]TTAAATATCTATAAT | 5521 |
rs146467563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885513 | CAGAACCTTCAAATC[C/G]TACATTGCTTCTGGG | 5521 |
rs146469129 | snp | C/T | 0.0126979 | 0.078662 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923258 | TTCCAGAAAAACAAG[C/T]ATGACAGAGGTCTGA | 5521 |
rs146481812 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656152 | TGTATGTGTACATGA[A/G]GAAAACCTGAGTTGG | 5521 |
rs146484140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050584 | TAACAGCTGTGTGAA[C/T]TTAGACTACTTAACT | 5521 |
rs146500423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652848 | ATATAATCAAATCCA[A/G]GTTTTGACTAGATCA | 5521 |
rs146524607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053749 | GACTCAAAAACAGAC[A/G]GCACCTATCATGTGT | 5521 |
rs146536641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902693 | CTGATCAAGCCAAAA[C/G]CCATCTGTGGTTCCC | 5521 |
rs146538556 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974968 | TGCTGGGACTACAGG[C/T]GTGAACCACCGTGCC | 5521 |
rs146538691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859364 | CTGCTAATGTATCAA[A/C]CTGTTTGGAGAAGTT | 5521 |
rs146554657 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792789 | CAGCAAGAAGGCTAC[A/G]GGACAGGCAGAAAGC | 5521 |
rs146556624 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994729 | GATGTTTGGCAGCCA[G/T]TCAGGCATGCATGTG | 5521 |
rs146562302 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799245 | GTTATTTGCACTAGC[A/C]TAATTTAAATTGTTA | 5521 |
rs146562813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754080 | TCTGAAAGTCCCCAA[C/G]ATATTTTGCCCACCA | 5521 |
rs146567101 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681085 | CATCAGTCGAAGCCC[A/G]GCTTGCAACGTACTA | 5521 |
rs146580240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863410 | CATTGATGAGTTCCA[G/T]TTTGCATGTCCCTAC | 5521 |
rs146581835 | in-del | -/GGG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706866 | GTCCAGGGAGCGGCT[-/GGG]GTTGTCAATGGACAG | 5521 |
rs146582352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796243 | ATCTTCATGATAGGT[C/T]CACGTATGCTCCCAT | 5521 |
rs146596857 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921392 | TTTGCCACATGGACA[C/G]GCAACAACAATTTCA | 5521 |
rs146603819 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638493 | ATTAGCAATGGCACC[A/G]TCTTATATTAGTAAA | 5521 |
rs146604429 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031031 | CACGAGGTCAGGAGA[C/T]CGAGACCATCCTGAC | 5521 |
rs146607243 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635586 | GGCTTCCCGTGCCAT[C/T]CCTGGCCTCCACCCT | 5521 |
rs146628987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915669 | TTAACGACTGACTCA[C/T]AGATTCACTGGCCTT | 5521 |
rs146643995 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035328 | ATGAGAACTCTATCA[C/T]GAGAACAGCAAGGGG | 5521 |
rs146655608 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600224 | GTAAACCTTTGGAAG[C/T]AGGGGCTGACTTAAA | 5521 |
rs146656001 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841503 | TCCCTATGGGCAAGA[C/T]GTAATCACAACCCAG | 5521 |
rs146656359 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049110 | GAGCATGTGTGTGTG[-/GT]TGTGTGTGTGTGTGA | 5521 |
rs146656446 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956079 | ACTGAGCCTGGCCCA[A/G]TAGTCTTCTTTCTAA | 5521 |
rs146682790 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738354 | TGAGCCGAGATCATG[A/C]CACTGCACTCCAGCC | 5521 |
rs146722549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620655 | GGCTCCGGGAACCCA[A/G]TGGCAGCATCCCCAG | 5521 |
rs146726916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617619 | GCAAGAGATATACCA[G/T]GCCTACGCTCCTTCA | 5521 |
rs146732190 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780207 | ATCTCTGGGATTAGT[A/G]CCTCAAAATCAGAGA | 5521 |
rs146735689 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809021 | CACTTCTCCAGTGAT[A/G]AATGTCCTTGGGTCC | 5521 |
rs146740232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693998 | CTCCTCACCTGACTT[G/T]TTGCCACCACCTCCC | 5521 |
rs146742970 | snp | A/G/T | 0.000148896 | 0.00862712 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650632 | ATAGTCGCTGTTGAC[A/G/T]GATATGGAGTTGATG | 5521 |
rs146750073 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900032 | CTTCAAAGTTCCATG[A/C]AAGAACAACTCAAAC | 5521 |
rs146751004 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967677 | CCCACTCAGTAAAGC[A/G]CTTCCCAGAATGTTT | 5521 |
rs146752679 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704343 | AATAAGGTAGCAAGT[C/T]TAGAGATAATAACGT | 5521 |
rs146770657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010742 | AACAGGCCACGGATC[A/G]GTAGTAATCTGTGGC | 5521 |
rs146771591 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010372 | GCACTTTATTTCTAT[C/T]TTTATTGTATTGTAA | 5521 |
rs146779083 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935752 | ATGTCTTCAGTGTAA[A/G]GTTTGGAAAAGGGTA | 5521 |
rs146791074 | snp | A/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006239 | GCCTAATAATTGGTC[A/T]GCTCAAACGTGGGAG | 5521 |
rs146791594 | in-del | -/A | 0.345925 | 0.230864 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835275 | CTTATATTTTGAGGG[-/A]AAATATTAAAATATT | 5521 |
rs146796236 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824618 | GACACACACTGTGGT[A/G]GAGTGGTAATTTTTG | 5521 |
rs146803404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792285 | AAATTACTGGCCAAT[A/G]CAGTGACAAAATGTT | 5521 |
rs146805371 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718403 | AAAAAAAAAAAAGTA[C/T]GGTTTCCTAGAATAT | 5521 |
rs146821815 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826826 | TTTAATCTTTCTCTG[C/T]ATACATATCACTTCT | 5521 |
rs146835551 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989599 | AAAGGAACATACCTC[A/G]ATACAATAAAGGCCT | 5521 |
rs146841643 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680353 | TGGACAATGAGATCA[C/T]GTGGACACAGGAAGG | 5521 |
rs146844909 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595985 | CCAACTCTATTGGTC[C/T]GTTCTTATATTTCAA | 5521 |
rs146851498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889838 | AACTTAGCAGTTGTC[C/T]AACTCCAGGCAATGC | 5521 |
rs146859998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795973 | CAACTGGGTATAAAC[A/G]TGCCTGCATATAGAC | 5521 |
rs146860743 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723419 | TGATAATCTCTGGGC[A/G]AGGGAGAATTAAGTA | 5521 |
rs146861639 | snp | G/T | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817030 | ACCCTGGAGGCTTGT[G/T]GTGATGAGCGTTGCT | 5521 |
rs146862486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673995 | GGCAAATAAACTCTG[A/G]CCATACGACCAAGTT | 5521 |
rs146863151 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775956 | ACTGAAAACTACAAA[A/G]CATTGCTTAAAGAAA | 5521 |
rs146872843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884300 | TAATGTTAAATAACT[C/G]TTAAAATCCTACCTT | 5521 |
rs146873218 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950903 | TATTTAATTCTTAGT[G/T]CCAAAAATTTTCGGC | 5521 |
rs146878580 | in-del | -/TG/TGTGTG/TGTGTGTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049100 | GAAAGGGAATGAGCA[-/TG/TGTGTG/TGTGTGTG]TGTGTGTGTGTGTGT | 5521 |
rs146887037 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075140 | AAGTTATCTGATATC[A/G]AGTGGGAAATTTTTA | 5521 |
rs146891903 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993524 | TGGGATTACAGGTGT[A/G]AGCCACTGCACCCAG | 5521 |
rs146900024 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055504 | CCTTGTACAAGACAG[A/T]CTGATTTCAGAAGCA | 5521 |
rs146902849 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977625 | GTGAGAACATGCAGC[A/G]TTTGGTTTTCTGTCC | 5521 |
rs146922601 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971743 | CAGCATTTCCAACAT[A/G]TTAGGTTATCAAACT | 5521 |
rs146934379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703401 | GGCTCTTGTCTCAGA[G/T]CTACGTTCTAAAGTT | 5521 |
rs146937501 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624172 | CTGGGTTTTCAGGAG[C/G]ATCAATGAAGATAAA | 5521 |
rs146944104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865710 | TGTGAGGACTCTAAT[A/G]AGCTGTCAAACATTC | 5521 |
rs146947198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907074 | GGTGAGGACAGAAGA[C/T]AGCGCAGGATGCCAT | 5521 |
rs146948919 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797723 | ATGGGGGACTCCTGA[G/T]AACCTAATTTTAAAA | 5521 |
rs146952085 | in-del | -/TTGTT | 0.489434 | 0.0719116 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861854 | CTTTAAAATACAGCA[-/TTGTT]TTTTTTTTTTTTTGG | 5521 |
rs146958591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977167 | CATTTTTCACCCCCC[A/G]ACAAGGTCCAAGCTC | 5521 |
rs146981421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760473 | TCTCTGCTCTCCAGC[A/T]ACTCATACTCTTGCT | 5521 |
rs146984556 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800119 | CAATCATGAAAGAAA[G/T]AATATGGATTTTTAT | 5521 |
rs146994014 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871026 | TGACAAAGTTCCTAG[G/T]GGACTTATAAAAATA | 5521 |
rs146996272 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615879 | ACTTTACAGAAATAG[-/A]AAAAAACAATCCTAA | 5521 |
rs147003779 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036981 | CTCATTTAATTCCAC[A/G/T]TTAATCCTATACAGT | 5521 |
rs147017554 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763184 | ACTGGCATCCAAAGT[A/G]CTTTTGCTCCACGAC | 5521 |
rs147019310 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639886 | GATAACTGCAAATGC[A/G]TGTGCCAGGAGTTTA | 5521 |
rs147019707 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690051 | AAGCATACAATGACC[A/G]TCCCATTTTGGCTTT | 5521 |
rs147027598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999249 | AAAGATATTGATTAA[A/G]TGGTCACACAAATAA | 5521 |
rs147027732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952879 | TGGATGGTTATCCAC[C/T]TCAGACAAAATGTTA | 5521 |
rs147029638 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082026 | AGCATGAACATTCCC[C/T]TTCAATTCAACTAGG | 5521 |
rs147040581 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685882 | CTGCAGCCCTCACCC[C/G]CCGCCTTCCACCCCA | 5521 |
rs147051834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847173 | TCTACCTCTATCTCA[C/T]TGTTTTCCAACAATA | 5521 |
rs147063764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957920 | GAAGAAAATACTATA[A/G]TTACAGCCTATGGTG | 5521 |
rs147066498 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945844 | AACCATTGTTTCCAA[-/T]GAATGAGCTGAGACA | 5521 |
rs147068373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890067 | TAACTTTTGTTTTGC[A/G]TCATATGCACCACTT | 5521 |
rs147085175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743164 | ACTTTGCTTATATCA[C/T]TTTACTCTCTTAACA | 5521 |
rs147101179 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849403 | TTATCTGTAAATTCT[C/G]ACTCCACTAGTGAGA | 5521 |
rs147122204 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747221 | GGCTCTTGTCTCCCA[A/G]TGGTAGGCAGTTTAG | 5521 |
rs147123626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621295 | ATCTGCCAGGCACTG[C/T]GCTAAACTCTTTATG | 5521 |
rs147148447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821943 | AATGGCAAAATACAC[A/T]CTGACAACGTAAGTA | 5521 |
rs147152808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753385 | AGAACCTTACACAGA[A/G]CAGGACCTCAATAAG | 5521 |
rs147159003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715793 | TTATTTCTTGTTCCT[A/G]TTCTCTTCTGTATAC | 5521 |
rs147172222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825385 | TCTCCTAGTATTCTG[C/T]TTTCCTAACAAGCTT | 5521 |
rs147181704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070083 | TGTGAGCCACCACAC[C/T]AGGCCCATTTTATAT | 5521 |
rs147190566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676861 | ACCGAGGTGGTGCTT[A/G]TGTTCTTAATTGGTT | 5521 |
rs147220612 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944416 | TTAGATTATGCAACC[C/G]AAGGAAACGCCAAAC | 5521 |
rs147230691 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073884 | TTACTAAAAATACAA[A/G]AAGTAGCCAGGGGTG | 5521 |
rs147239969 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808304 | GTCACATGTGCCTAG[C/T]GGCTACCATGTTGAA | 5521 |
rs147252449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876251 | TAAAAATAAGAACAA[C/T]GGTAATATCCAGGGC | 5521 |
rs147255016 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917871 | CAAGGATGCGAAGTA[C/T]CTGTTTAACAGTAAA | 5521 |
rs147256435 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805835 | TGCTTCACCTGTGAT[C/T]TACACCTGACAAGCA | 5521 |
rs147263032 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771146 | TCTTTATATCTTAGA[C/T]CCAAAGCTCCCAGTG | 5521 |
rs147264023 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695254 | AGTGGTTCTCTCTGG[A/T]TGGGAACACTTTTAT | 5521 |
rs147286460 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047973 | ATTGTTGAGTTCTTA[C/T]CTCTGACTGTACATA | 5521 |
rs147291929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965908 | ATCCTCAGATCCTTC[A/G]TCTATAAAGTGGGAA | 5521 |
rs147297583 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654160 | CAGTCACTGAGTTTA[C/G]AACCCCTGACTCCCT | 5521 |
rs147301303 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651079 | TTAAACATGAAATCT[A/G]TTTAAAAAAGGGAGT | 5521 |
rs147312522 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687651 | GATTATTGCTTTATG[-/T]TAAGTTATGATATTG | 5521 |
rs147324562 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862416 | TGACGTGCAGGATCT[C/G]TGTCTTTAGATCTAG | 5521 |
rs147324689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928981 | GAGCCTTTGCATTGG[C/T]TATTTTCTTTTCCTG | 5521 |
rs147327883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972259 | CCTCCTCATGTCATA[G/T]CAGATGGTAGGTGTT | 5521 |
rs147328655 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925732 | TTCAAATAGGTTTTC[C/T]GTCCCTTTCTCTTCT | 5521 |
rs147336728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051946 | ATGGCTTCTTTACAG[C/T]TATGATTGGAATTTT | 5521 |
rs147347143 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794592 | AGCTTCTCAGAAATG[A/C]GCATATAACTCCAAT | 5521 |
rs147349728 | in-del | -/AACCCCCC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754151 | GATTGGAAATTACAA[-/AACCCCCC]CAGCCGTTCTGGAGG | 5521 |
rs147358922 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901144 | CACACCCAGTTTTGA[A/G]GTTGAATATGACCAA | 5521 |
rs147362132 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857604 | AAGATTAAGGTTAGT[A/G]TATTAACTTATTTGT | 5521 |
rs147362436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791433 | CACGTGTGCGTGTGC[A/G]TCTGTACAGCTTACA | 5521 |
rs147370281 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752174 | TGAGGGTGGGGAGAG[A/G]CTGATCAGCTTGAGA | 5521 |
rs147371388 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677691 | CACCACCATGCCTGG[C/T]TAACTATTGTATTTT | 5521 |
rs147383897 | snp | C/T | 8.3462e-05 | 0.00645941 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600447 | GTTGCTTGGATCTTC[C/T]GGCTCTTCAAAAACT | 5521 |
rs147384928 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861414 | ACCAGGATAGTCTCA[A/G]TCTCCTGACCTCGTG | 5521 |
rs147391731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026568 | AAAACTTATGTACTT[C/G]TGCATTTTATTATGT | 5521 |
rs147398133 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948967 | AGAAAGGGCACCCAT[A/G]GAGCTTCTGAAACAC | 5521 |
rs147404240 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637111 | CCTGGGTGCATCTTG[C/T]CTCATTAGCCAAATT | 5521 |
rs147406083 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756972 | AATTAAGATTAAGGA[A/G]GGTAGACAATGGAGA | 5521 |
rs147407998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682207 | AGTGAATACACTCTG[A/G]ATGCAAGGCAGCGTA | 5521 |
rs147409782 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074216 | AGTATCCTGCCTAAG[C/G]TCACTAAGTGGGTAA | 5521 |
rs147430872 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912879 | TAAGTCTCTTCAATG[C/T]GTCAAGTACTACCGT | 5521 |
rs147441076 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032490 | GCACCATATTTATAG[C/T]ATTTTAGCTCTCACC | 5521 |
rs147451357 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777009 | TAAGTATTGTCAAGG[A/G]TGTGGAAAAATTGGA | 5521 |
rs147466527 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839421 | GCTACTCGGGAGGCT[A/G]GGGCAGGAGAATCGC | 5521 |
rs147466540 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886090 | ACGCCTGTAGCCCCA[A/T]CACTTTGGGAGGCCG | 5521 |
rs147474873 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736611 | TCTTGAGGACATCTC[C/T]GCCATCTTCTTCCCA | 5521 |
rs147489272 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843519 | ATTTGTAACAGATTA[A/C]TGTAGGATTAGAATA | 5521 |
rs147490633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654652 | ATCCTCAATAATATC[A/G]TGCTGAAAGAACTAT | 5521 |
rs147496726 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619300 | CAAAACCCCGTCTCT[A/G]CTAAAAAAAAAAAAA | 5521 |
rs147497293 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004766 | GCCTTAAGCCTTCCC[A/G]CAGGATGAAACTTTT | 5521 |
rs147511678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739508 | CATTTGGGGACCAAC[A/C]GAGATTTCAATGAGA | 5521 |
rs147513568 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616122 | AAAGGTGCCAAGAAC[A/C]TACACTGGGGGAAAA | 5521 |
rs147514054 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659816 | AGCCCCTATGGTAGC[G/T]ATTATTAGCATTCTT | 5521 |
rs147524300 | snp | A/G | 1.65348e-05 | 0.00287526 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600298 | TTCTATACCTGGTAA[A/G]TCTCGATGGGGCGGT | 5521 |
rs147530719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965515 | AGAAAATAATGACAG[C/T]GTGCCCTCCATTCCT | 5521 |
rs147533219 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897727 | AAATCCTAATTTGTA[C/T]GTGCAGAAACATTTA | 5521 |
rs147534232 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037402 | GAGACAGACAAAGGG[-/GT]GTGTGTGTGTGTGTA | 5521 |
rs147547417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008978 | GGCCTCTTTACTGAT[C/G]TATGCTTGAATGGTG | 5521 |
rs147547499 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962440 | AAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTCG | 5521 |
rs147558057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711246 | ATCTTTTTTTTTCTA[G/T]GCTCACAAGTCATCA | 5521 |
rs147560175 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634437 | TATCCCAGGTTCAAG[C/T]GATGCTCCTGCCTCA | 5521 |
rs147563196 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630044 | GTCTCGAACCTCCTG[C/G]CCTCAAGCAACCCAC | 5521 |
rs147584614 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936616 | AACAGAACCTCTCTG[A/T]ACAGAGAGATAGTAA | 5521 |
rs147597651 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061536 | CTACAGGGACACAGG[G/T]TATGTTGTCTTTCTC | 5521 |
rs147600331 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980771 | GAATGTTTTATACAT[A/G]CATAGGAGAATTGCT | 5521 |
rs147607197 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874056 | TTTAGTTCTCAGTTT[C/T]AGCTGTCTGAGAGGC | 5521 |
rs147620551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066374 | TTTAATCCTCACAAG[A/G]GCCCTGGATGTAGCT | 5521 |
rs147628854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767811 | AGGGTTTGGACAAAT[A/G]TAGCATGACACGTAT | 5521 |
rs147640303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837227 | GTTACATGAGCTATT[C/T]GAACTTTAAAAATAG | 5521 |
rs147647307 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763307 | CACCAAGGGACAGCT[G/T]CCTAGCGTATAGGAT | 5521 |
rs147663996 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693102 | TCAGTAGGTACATAA[A/C]CCTTCCTCCCTTCCC | 5521 |
rs147668908 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082280 | CTCATATGCTCTTCT[C/T]AGTGTTGTTGACGGG | 5521 |
rs147680469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689898 | GCTCAACTGAAGACC[A/G]TGTGCCCATTAGGAC | 5521 |
rs147686578 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647243 | TAGAAGCACATTGCT[C/T]ACCATCCCCAGTAGT | 5521 |
rs147689705 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921032 | GGGTGCAGGGTACAG[C/T]ATGTTGTCTCTGGTC | 5521 |
rs147689706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962966 | GCACTCAGACTTTCT[C/T]AGTGGAGCTGAATAG | 5521 |
rs147700309 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039618 | CACGGAGACCATCTA[C/T]GAAGGCTACTTGCAG | 5521 |
rs147705779 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960425 | CTCCTGAGTAGCTGG[A/G]GTTACAGGCGCAGGC | 5521 |
rs147712266 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923158 | TTTGAGCCAGATTTT[C/G]TCTGACTTGACACTA | 5521 |
rs147713257 | in-del | -/TGT | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907911 | AACTGGCTGATCAAA[-/TGT]TGGCAGCATTGAATT | 5521 |
rs147723208 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044860 | TAAACATGATATGAA[A/G]ACATTCTTAGTGGTT | 5521 |
rs147724048 | in-del | -/AGAT | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594001 | GTTTAGGGAAAGAGC[-/AGAT]AGATAGGACTTGGGT | 5521 |
rs147727380 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854220 | GAAAATCAGAGAGAG[C/G]CCTACAAGGCTTCAT | 5521 |
rs147743968 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819579 | AAAAACTAGCTCCAT[C/G]TAGCTTTGGAATAGT | 5521 |
rs147747404 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816679 | ATCAAATAAAAACAC[A/C]GGTTTTTTATTAAAC | 5521 |
rs147751635 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747305 | AACTGGAAAGATCCC[A/G]GTAGAGCAGCTTTGG | 5521 |
rs147767675 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672741 | CTGTTCTATTTGAGT[A/G]TTCATTTAACACTTT | 5521 |
rs147767915 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624072 | GATGTAAGAAAAAAA[A/C/G]CCAATCATTGTCAGT | 5521 |
rs147768502 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066694 | ATAAGAAAGATATGG[C/T]CCCTGTCTTAATGCC | 5521 |
rs147781486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747107 | ATTAAATTTTAAGAG[A/G]AGCTTCCCAAATTGC | 5521 |
rs147784186 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669918 | GTATAAAGAAGATTT[A/G]TGGATTATCTAGATC | 5521 |
rs147784621 | microsatellite | (A)9/10/11 | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667575 | TTCCTAAACTTACTT[(A)9/10/11]CCCAAAAGGATTACT | 5521 |
rs147790931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629687 | CCAGCCTACCTCTCT[A/G]GCTTCACTTTCCTTT | 5521 |
rs147791299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903802 | TGACCCCAGGAAAGT[C/T]AAAGTTGTATCAGAA | 5521 |
rs147794348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944844 | AGGGAAGAAGAAAAC[A/G]AATGTCTGATCTGGT | 5521 |
rs147805782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017765 | AATTAGGTTTAGAGT[A/G]AGAAGGAAAACAAGA | 5521 |
rs147808097 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940912 | TTCCATAAGCCGTAG[A/C]CTTCTCCTGGAAGTA | 5521 |
rs147817196 | in-del | -/TTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976109 | CATTTTTTAAAAAAT[-/TTA]TTATTATTATTATTA | 5521 |
rs147817583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906917 | GCAGCTGATTAAATT[G/T]AAAGAGACAATCTAC | 5521 |
rs147829003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022579 | AAAAATCCAAATTTA[A/T]TAAGAAAATAAAGCC | 5521 |
rs147831539 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838184 | GTCTCTAATACTTAT[A/G]TTGTGACAAACTTTC | 5521 |
rs147838050 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802866 | TTATGCAAGTATTTT[A/G]AACCCACAGGACTTC | 5521 |
rs147855092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799737 | TGATTGTAATTTCTG[C/T]ATATTTTAACAGATG | 5521 |
rs147859251 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925026 | TAACTCCAGAAAATA[A/C]AAGAAGTTTGCTCCA | 5521 |
rs147865896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045230 | TTAAAATACATTCAT[A/G]TACTGCATAATGACA | 5521 |
rs147873893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600901 | ATAATCTAAATTTAG[A/G]ATATGTTCTTTACCT | 5521 |
rs147887795 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728868 | TATAAGTCCAATTAA[A/G]CCTCTTTTTATTTCC | 5521 |
rs147910327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606488 | TCCAAGCTTCATTTA[A/G]TGGAGATAATAGTAG | 5521 |
rs147914163 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923366 | CTGGATTGCATGATG[A/T]ATGGCAGTGATCTTC | 5521 |
rs147915640 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999062 | CTCTGGTTTTGAGAT[A/C]TTTCCTGTGCAATTC | 5521 |
rs147923024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893120 | CCATCCATTTATTCC[C/T]TCGTGATGTGTTTCT | 5521 |
rs147932241 | in-del | -/C | 0.106987 | 0.205054 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762919 | ACATGTGTGGAATAT[-/C]ACCAACATCTGACTA | 5521 |
rs147943756 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743082 | ACACCACCCACTTTG[C/T]GGTACTTTGCTATGG | 5521 |
rs147943879 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788769 | ATGGTGAAGGGTACT[A/C]TTTAAATATAATCCT | 5521 |
rs147956784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852502 | CCGTTATCAGGCCAC[A/G]AGCAGGACTTAAATT | 5521 |
rs147957267 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894896 | TTTCTCTCCTGTAAG[A/C]TCTTTGGGGCCAGGG | 5521 |
rs147959592 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849012 | TGTCCTTTTGACATA[C/T]CTCCATCAGTGCAGG | 5521 |
rs147960424 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784724 | AGAAGGATGACTGCC[A/G]TGTTGATTTTAAAAC | 5521 |
rs147975236 | in-del | -/GGGGGG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630696 | GCTGTGAATACGGCT[-/GGGGGG]GTTGACATTACTACT | 5521 |
rs147978901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055357 | CTTGACACTGGTTCC[A/G]ATGACTTGTTTGCAT | 5521 |
rs147993314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608579 | AGGCAGGTAGATCAC[A/G]AAGTCAGGAGCTCGA | 5521 |
rs147995972 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729984 | CTCTAGACCCCATAA[C/T]GGTAGATCCACTGAC | 5521 |
rs148006907 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800127 | AAAGAAATAATATGG[A/C]TTTTTATAGCTCTAG | 5521 |
rs148014825 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008375 | AATGTTAATTTATTC[A/T]TAAAATATTTTAATT | 5521 |
rs148019802 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933045 | CGTGGGAATTATATC[A/G]TATGCTGTTTTAATT | 5521 |
rs148026680 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790933 | AGAGTAGATACACAA[A/G]TGGAGCAGAAAGGAC | 5521 |
rs148035054 | in-del | -/G | 0.0256215 | 0.110247 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782519 | TTCAGCCTGAGTGAT[-/G]GACTACCTGATTCCT | 5521 |
rs148037269 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079114 | CTTCTAAAGCCCCTA[A/G]GAAGACAGATAGAAA | 5521 |
rs148045378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686718 | TCAACCTGGCCTAGG[G/T]TCCCAGGGCACTGGC | 5521 |
rs148047152 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601962 | GAGCCCATCACAAAC[G/T]GCCTCTAATTCTTTC | 5521 |
rs148054034 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893692 | ACACAGGGAGGGCAA[C/T]ATCACATACCAGAGG | 5521 |
rs148078313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890192 | GTCTTTCAAAACTCA[C/G]CAGGGCCAGCCCTGG | 5521 |
rs148079219 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817549 | TTTTTTATTGTGAGC[A/C]TTTTCCCTTTTAATG | 5521 |
rs148082984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591223 | AGGAACTCTCGTGTA[C/T]TTCTCAAATGATTTG | 5521 |
rs148083985 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986648 | AGGGTCTCAATAGCA[A/G]AACTGATTAAGCAGA | 5521 |
rs148097153 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718736 | AGAGACTGGGTGGGA[A/G]GATCTTTATATGCCA | 5521 |
rs148099442 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639775 | ATTCACTTTTTTCTT[C/T]ACTTAGCTTTATCTA | 5521 |
rs148101506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659863 | TGTAGAAAAATGGTC[C/T]ATTCTGAAAGATTGC | 5521 |
rs148115596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781202 | CATGATATAAGTGAA[G/T]AAACTAAAACAGACA | 5521 |
rs148117840 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705191 | TTCATCTAAGAAACA[A/T]TTGGTAGATAATATC | 5521 |
rs148120763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943723 | AGAGAGAAGTATTCT[C/T]TCCCCAGAGAAAATC | 5521 |
rs148130704 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884693 | TACCTCTTACCATTC[A/G]TTGGTTTTAGAGTTA | 5521 |
rs148137867 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981519 | AATTTTTTTGTTTAA[-/T]TAAATATTTTTTCCT | 5521 |
rs148140397 | in-del | -/GA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986215 | AATCTATCAGTTTGG[-/GA]GAGAGAGAGAAAAGT | 5521 |
rs148148390 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059348 | GAAACACCTCCTGTT[-/A]AAAGGCAATTATCTT | 5521 |
rs148154234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735457 | TATTACATAATAATC[C/T]CAGAGCCTCAGCTTG | 5521 |
rs148155551 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653868 | TGGAGAGCTGAATGC[C/T]GCTCGTGGTATTCCA | 5521 |
rs148162898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829007 | TAACATAGAGAAGAA[C/T]GGGTAAGTGAGCTGA | 5521 |
rs148167752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842171 | TTTGTTCACTCCAAC[A/C]TTTACCTTCTTCCAT | 5521 |
rs148171230 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775729 | ATTTAAAAACCTTAA[A/G]AACACAAACACACAC | 5521 |
rs148209319 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690642 | CTGTGTTCACTGTTT[C/T]GCAGATGGAGAAATT | 5521 |
rs148219078 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764848 | CGCACACACACACGC[A/T]CACGCACACGTACTC | 5521 |
rs148222609 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803505 | AATTTATTTATGTTA[A/C]AAGAAATACTGGGTA | 5521 |
rs148228646 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050890 | CTGGAAGATACTTGC[C/T]TTAAGATATGTCCTC | 5521 |
rs148239759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821167 | ACAATCTCCAACACC[G/T]ATATATATATCCACA | 5521 |
rs148247363 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037591 | TGTGTAAAAGTATGT[A/G]TTGAGTGAGCAAGAA | 5521 |
rs148250962 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927986 | ACCTCGTGATCCACC[C/T]GCCTTGGCCTCCCAA | 5521 |
rs148258231 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645335 | ATCTCCAAAGAGGAC[A/T]CCAAGGGATATTCCT | 5521 |
rs148268228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923553 | AGCACGATCCCTAGT[A/G]GGTTTGTCGGAAGCC | 5521 |
rs148287850 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947892 | TCTTTTCCTCAAGGC[A/G]AAATCCCACTAATCA | 5521 |
rs148289644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850603 | CTTCCCATCTCCTCT[G/T]CAACAGAGCTAACTC | 5521 |
rs148294461 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635891 | GGCATTTACTATCTA[C/T]AGGGGAATGACATTG | 5521 |
rs148298376 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025853 | ATGTTAGCATTTAGA[A/T]GTAAGCAAATAAGAA | 5521 |
rs148303461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960977 | ATTCTTCATCCCACC[A/G]GAGTCAACCAGGCTT | 5521 |
rs148306965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786224 | ACTCAAGATATGTAG[A/G]ATACTATTGAGAAGG | 5521 |
rs148307235 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756170 | TGAATCAGTAGTTTT[A/G]TAACATAAGCCGCTG | 5521 |
rs148310941 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681532 | TAATTCAGATAATTT[C/T]ATCTGAAAAATTCAG | 5521 |
rs148343990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846960 | TCTTATCTCATGCAG[A/T]TCTTAGAACATTGTT | 5521 |
rs148346598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631906 | GTGTCCATGACCTCT[C/T]TCCACTCTTACCTCC | 5521 |
rs148347904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019789 | AGATGTTAAAGCCAT[C/T]ACTTAAAGATGATTT | 5521 |
rs148351763 | snp | A/C/T | 3.36113e-05 | 0.00409936 | intron-variant, synonymous-codon, missense | PPP2R2B | GRCh38.p7 | 5:147055715 | GGAGGTCTGAAGATG[A/C/T]AAGGCAGGTAACGAG | 5521 |
rs148364794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694876 | CTTAGTTTACAGTAT[A/G]CATTTGCCTAATCAT | 5521 |
rs148367153 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619097 | AGGTCTGACCCATCT[A/G]CTACTCATTTGCACC | 5521 |
rs148370782 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866186 | CTGATCCCTGCTCTA[G/T]AACATCGACATAATT | 5521 |
rs148381123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739489 | AGACTCATAGAACAT[A/G]GTACATTTGGGGACC | 5521 |
rs148388927 | in-del | -/GTCTT | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590837 | ATGGATGTCATCATG[-/GTCTT]GTCTTATCTAGGAAA | 5521 |
rs148389108 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904612 | GCTTGAGTAATGGTT[G/T]TAACCACTGATCATA | 5521 |
rs148390292 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891778 | ATAGCTTTGACAGAT[A/G]AAATAGATGATCAGA | 5521 |
rs148394211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819493 | TGTGGAGATGGCAAA[C/G]TGTCAACTCCTGACC | 5521 |
rs148397318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988861 | AAAACGAATAATCCT[C/T]TAGTTAGGCTAATAA | 5521 |
rs148397891 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071310 | TGAAAAACTGGATTA[C/T]TGCAATAACCTTTCA | 5521 |
rs148409045 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925590 | GATTTGGCATACAAC[A/T]GTTTGACAATGATGT | 5521 |
rs148410834 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720866 | ATCTGACTATAGAAT[A/G]CTACTGAAAAATACT | 5521 |
rs148423117 | snp | A/G | 5.01081e-05 | 0.00500515 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600448 | TTGCTTGGATCTTCC[A/G]GCTCTTCAAAAACTG | 5521 |
rs148433998 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677757 | AGTCTTGAACTCCTG[A/T]GCTCAAGCGATCCAC | 5521 |
rs148436264 | in-del | -/TG | 0.0345262 | 0.126772 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920760 | TGTGTCCTTTTATGC[-/TG]TGTGTGTGTGTGTGT | 5521 |
rs148445420 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886288 | AGCTTGCAGTGAGCC[A/G]AGACTGCGCCACAGC | 5521 |
rs148463520 | in-del | -/G | 0.029116 | 0.117091 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059495 | TCATTATAAGGAGAA[-/G]GGAGGATCTAAAGCA | 5521 |
rs148474587 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016771 | CATTCTATCCAGGCA[C/G]AAAACATGTCATAAT | 5521 |
rs148481216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655424 | GGAGGCCTTCCGTGA[C/T]CATCCCACCTCAAAT | 5521 |
rs148487491 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672054 | ATAAGTGGTGAAGAC[A/G]GAAGCCAGGCTGCTG | 5521 |
rs148490493 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940016 | TCTACCTACACCTAT[G/T]TTTTATATAATGTAT | 5521 |
rs148494564 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844591 | AAGACCTGCATGCCC[A/G]GATCCATTCTGTGCA | 5521 |
rs148495798 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667218 | GGCTGAGCTGAATTT[A/G]AATGTAGTGATTCTA | 5521 |
rs148516865 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651440 | AAGTATTTGTTGAAT[A/G]AGTAAGAATACATGA | 5521 |
rs148527704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836014 | GATAACACCACCAAC[C/T]GCATTGGGTTGTTGG | 5521 |
rs148532247 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766818 | TAGCACTTTGGGAGG[A/C]CAAGGCGGGAGAATC | 5521 |
rs148542883 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974374 | ACATTAGAAAATGGA[G/T]GTCCAAGGAGTATGA | 5521 |
rs148543948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875990 | TGGTATTTACATCGT[C/T]TAAGTTCTATTTTCC | 5521 |
rs148549140 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823358 | GCCCACCACAAGGCC[C/T]GCCTAATTTTTTTTA | 5521 |
rs148564633 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800917 | GGGGTATGTGTACAT[-/AC]ACACACACACACACA | 5521 |
rs148564871 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931059 | ATTGTGCCAAAGATA[A/T]TTTTTTTTTTAGTGC | 5521 |
rs148576531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046882 | GCTAAGTTCCTTATG[G/T]ATTATACTAGAAACT | 5521 |
rs148605805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028669 | ATGTCTTTTGGTGAA[C/T]ATATGTATGTGTTTC | 5521 |
rs148613049 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962412 | GCCTGTAATCCTAGC[A/C]CTTTGGGAGACCAAG | 5521 |
rs148615033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043024 | CCTTGTAGCTTGTTT[A/G]CGTTATTTCTAGGCT | 5521 |
rs148619116 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757760 | GACTATCCTGTGGAA[C/G]CAAACTGCAAGAAAG | 5521 |
rs148620174 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683185 | GTACCCTTCCTACCC[C/T]GCCTTTTCCCAAAAT | 5521 |
rs148622752 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074886 | TTTCAGAGGGAGGGA[A/G]GGAAAAAATGTGATG | 5521 |
rs148638399 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746725 | CTCTTGGGCAAAGCT[A/G]CTTGAACTGATAATT | 5521 |
rs148643546 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637558 | TCCTTCTGCCTTCCA[C/T]CTGAACAATTTCCCT | 5521 |
rs148647362 | in-del | -/TGATATACGATCC | 0.0763149 | 0.179815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834714 | GTGTGTGTTGAGACT[-/TGATATACGATCC]TTGTCACCCAAGTAG | 5521 |
rs148653672 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918817 | TTTTTCCTGAAGAGG[C/T]TATCTCCAGTTTTCC | 5521 |
rs148659251 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022101 | ATAAAATTGAAGATG[A/G]GGTATAAAATTATTC | 5521 |
rs148661610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991641 | AATACTTTACACCAA[C/T]TCAATTATTATACCA | 5521 |
rs148671641 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874825 | GGGGTTCCATATCTG[-/A]AAAAAAAAAATCAAA | 5521 |
rs148682297 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979837 | GTGAATGTGATCTCT[A/G]TCTCTCAAAATATCT | 5521 |
rs148686252 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772162 | TATGGGCTATCATGG[A/T]AAGATCTCCAAGACC | 5521 |
rs148689545 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695474 | TTTATTGAAATTGTA[A/T]GTTTGAAAATATATT | 5521 |
rs148695407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710407 | TTTGAATCAACCCAA[A/G]GACATGTGGGTTGAT | 5521 |
rs148697450 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906542 | GGTCAGACTGATCTC[A/G]AACTCCCGATCTCAG | 5521 |
rs148698250 | in-del | -/TGTGTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708408 | GTATGTGTGTGTGTA[-/TGTGTG]TGTGTGTGTGTGTGT | 5521 |
rs148701611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881787 | AGACAAACATTTCTT[A/G]AACAAATGAATAAAT | 5521 |
rs148732983 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623019 | GATCTCATCTCATTC[A/G]CTCATACATTCAATA | 5521 |
rs148734049 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009493 | TACTTAATCTAGAAC[C/T]TGACATGTTGTATAC | 5521 |
rs148739044 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801853 | CAAATTATAATTGCA[A/G/T]TAACAACTTCTCCAG | 5521 |
rs148741400 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732450 | AATAGAAAGGAGGCA[G/T]GATTTGGAATTTCCA | 5521 |
rs148755610 | snp | C/T | 0.00412965 | 0.0452523 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908777 | TTTCTTCCTTTCCCG[C/T]CCTCCCTTCCTCCCT | 5521 |
rs148757478 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858089 | GGCACCGTCACTTTT[A/G]ATACTTACAATAGCC | 5521 |
rs148770975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966052 | TATCTATTTCAGACA[C/T]AAAATGCAAGGAGAT | 5521 |
rs148776971 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898139 | GCAGTGAACTGAGAT[C/T]GCATCACTGCATTCC | 5521 |
rs148780961 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605358 | CCCTCCCAGCTGTTG[A/G]ATTCTAAAATCTATG | 5521 |
rs148783367 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049124 | TGTGTGTGTGTGTGT[G/T]AGATATTTTACATAG | 5521 |
rs148794990 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798226 | CAATTTCTTTCACTC[G/T]GTTGCCTCATTTTGT | 5521 |
rs148837818 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054728 | TTCCAAGAGAGTGTG[A/G]CTAGACATGAGTTGG | 5521 |
rs148841966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944856 | AACGAATGTCTGATC[C/T]GGTCTCTCAGAGGAG | 5521 |
rs148844192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768770 | GCCTCCTCCCAGCTC[C/T]TTCCTGTTCCTGGAG | 5521 |
rs148868213 | snp | A/T | 0.0854556 | 0.188216 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729166 | ATGGAAATGAGGAAC[A/T]TGTTGGGAACTGGAG | 5521 |
rs148879527 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932821 | AGAGCAGTGAGAAAA[C/G]GAAAACTAACCACCT | 5521 |
rs148882657 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838307 | AAGGGAGGCCGGGCT[C/T]ACACCTGTAATGCCA | 5521 |
rs148883656 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648417 | CTTCAGAGCTTTACT[A/G]TAACTCTTAAAATTA | 5521 |
rs148891352 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050172 | AAAATTCAAAAAATA[C/T]GTTTCAGACATAAAG | 5521 |
rs148906324 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601334 | CCAGGTGTGGTGGCT[C/T]ATGCCTGTATTCAGC | 5521 |
rs148920726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759941 | TAGTGTATTACAATA[C/T]CATATTTGTGCCTTC | 5521 |
rs148921786 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685605 | AGTCCTCATTCAGGA[A/G]TCAGAGCTGGTAAAA | 5521 |
rs148927827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923439 | GAGTTGATTCTCCCT[A/G]TGGCAGTCCCAAAGC | 5521 |
rs148928010 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854695 | GTGTATAGACACACA[A/C]TCACCTTGTACCTCA | 5521 |
rs148931318 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963292 | CATTGGGCTGACATC[A/G]CCTAGGGAATTTCAT | 5521 |
rs148935485 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869047 | GGTGCACAGAAAGCC[C/T]TCCATAACTACCAGC | 5521 |
rs148941263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045285 | TACGATGGTGATTCC[A/G]TAAGATTTTCAAATT | 5521 |
rs148946922 | in-del | -/CTC | 0.205723 | 0.246048 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848848 | TGCATGGGAGATTTT[-/CTC]CCTCCTCTCCTATTT | 5521 |
rs148980673 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920651 | TTGCTGGTACGTGTG[G/T]ACATGGAAGGAAGAG | 5521 |
rs148990808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039557 | GGGGCCTGAGAAATA[C/T]TTACCAGTAAGCACC | 5521 |
rs148999589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981254 | CTTACTGAAGTTCAT[A/G]CTTCAATCCCTCTTT | 5521 |
rs149001693 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775073 | AAGAATTAACACCAA[C/T]CCTTCTCAAACTCTT | 5521 |
rs149003803 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697036 | ATCACATTATTGACA[C/T]TGTATTTTTTCACTT | 5521 |
rs149007853 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711804 | GGGAGGTAATGGGAG[A/G]TTGGGATACAAGTAC | 5521 |
rs149010959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635167 | CTACTTTCAAATGAG[A/G]AATCTGGGGCTCAAA | 5521 |
rs149013793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884350 | TCCATCAGAGGAAAA[C/T]TGATGTCGTTGTCTG | 5521 |
rs149032661 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949966 | TGATGGTTACCAGAG[G/T]CTGGGAAGGGTAGTG | 5521 |
rs149046374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623980 | CTTAAACATGAGTCA[A/G]TTACACACACGAGAG | 5521 |
rs149046898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010895 | TTCATGGCCAGACTC[C/T]CACCATTGCTCTCAT | 5521 |
rs149049571 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985017 | AAATATTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 5521 |
rs149057328 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701690 | TGCTCCAGCTTGGCC[C/T]GTGCCCCTTCTTTTT | 5521 |
rs149068624 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911579 | TGTTTAAAGAAGGAT[A/T]TAAAAATAATATTGC | 5521 |
rs149070684 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840967 | AAACAAGACAAATAT[A/G]TATTAAACATTAGTG | 5521 |
rs149086181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900746 | ACCTAGGTATTAAGC[C/T]GGGCATGCATTAGCT | 5521 |
rs149091147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803332 | CAGGGAATGTTCTAA[A/G]AGAGTGCTGGGGATT | 5521 |
rs149096933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970456 | AAAAAATTAGCCATG[C/T]GTGGTGGCGGGCTTC | 5521 |
rs149106589 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799556 | TGAGACAACACATGT[C/G]CACTCATGAGTTTTG | 5521 |
rs149130682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724793 | AAGCAAGTCTATCTG[A/G]GAGTTACATGCAAAC | 5521 |
rs149138293 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893497 | CAGGTGTCATGTCCT[A/G]TAAATCCCAGATTCC | 5521 |
rs149143468 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831782 | AGCTTGGGTGACAGA[A/G]TGAGACTTCGTCTTT | 5521 |
rs149143952 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902729 | CATTGAGAACAACAT[C/T]CAAACTCCTTAAGCT | 5521 |
rs149148272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616703 | CCCTAGTTAAAATGG[C/T]TTTCATCTAAAAGGC | 5521 |
rs149163076 | snp | A/T | 1.67419e-05 | 0.00289321 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878017 | CTTCGGTCGCATAGC[A/T]GTGGTCGCGCAGGAA | 5521 |
rs149167282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681095 | AGCCCGGCTTGCAAC[A/G]TACTAGGATCAAAGT | 5521 |
rs149169131 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596747 | GCAAGTGATGTGGAG[A/C]CAAGCCCTGAAGTCG | 5521 |
rs149170587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073363 | ACAGCAAGCCTCCTC[A/G]TATCAAGACATTCTC | 5521 |
rs149176238 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786053 | CTTCTCAACATGAAG[A/G]AATAATAAAATCTTT | 5521 |
rs149182554 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791927 | TGAGGCCCTAATTGG[C/T]CTAATTCATCAGGTA | 5521 |
rs149190051 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956950 | CTCATCACCTCCCAA[A/G]GGTCCATCTCTTAAT | 5521 |
rs149190728 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889675 | AATCTGTAACCTTTC[C/T]GTATAAGTCATAACC | 5521 |
rs149193991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998283 | TCAGGGAGCACAATT[C/G]AGGTGCACACAGTGA | 5521 |
rs149195910 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663581 | TTTTTTTGGTTTCCC[-/C]AGTGTATATAAAGTT | 5521 |
rs149203642 | snp | A/T | 0.00478085 | 0.0486577 | synonymous-codon, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081126 | TGTGTCCTGGGTGAG[A/T]GTCCCAATTCCTGAA | 5521 |
rs149205090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019541 | GCTACAAAACCTGGT[A/G]AAGTGAGATCTAATG | 5521 |
rs149212712 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739363 | AATTAGGGGAAGCAT[C/G/T]GTGGAGAAAGCATTC | 5521 |
rs149214541 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990048 | GAAATATCTCTACAA[A/T]TAAAACCATAAAACA | 5521 |
rs149217897 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630843 | ATTCTAAGGCTCCAC[A/G/T]GGTGTTATTTAATCC | 5521 |
rs149219613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750905 | GAGACAACAAAGAAG[A/G]TCCCCACCCTCAGGG | 5521 |
rs149221666 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673771 | CTTTCTTAGCTCAGT[A/G]AGAACTTGAAAGTTT | 5521 |
rs149223316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067861 | ATTGTTCATGTTTGT[C/T]GATGATGTAGAGACA | 5521 |
rs149227399 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846592 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 5521 |
rs149232597 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762158 | AGAATTCCTTTAATG[C/G]ACAAAATGTTAAAGA | 5521 |
rs149238191 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653591 | GTGGCTCCTCCTAAA[C/T]TCTTCCCCGGGCCTC | 5521 |
rs149241489 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924900 | CTGCATAGTATTCCA[C/T]GGTGTATATGTGCTA | 5521 |
rs149243055 | snp | C/T | 0.0146672 | 0.084371 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857575 | CACCACCAGCCAGTA[C/T]TGATACTGGATCAAA | 5521 |
rs149244573 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828845 | CAGGTTATAAAACCA[A/T]AAACATCCAGATGAG | 5521 |
rs149247090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937686 | GCAGTTACACCTTCA[C/T]GGAGGCTTAGAGAAC | 5521 |
rs149251710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046626 | CAAAAGAGCACTGAT[C/T]AGTGTATGTTACAGG | 5521 |
rs149258075 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965374 | TGTTCAGAACGTTGA[A/G]GTTTTCTCTGATTAG | 5521 |
rs149268603 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594485 | CTGAACCCACTAGCA[C/T]GGAGTGGCAATAATA | 5521 |
rs149272080 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642036 | GACCTGACTGCTTAC[A/G]GCATTTCTTATTAAT | 5521 |
rs149282375 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720044 | CCCTCCTGAGGTTTT[C/T]CTCTACCTCTCTGCT | 5521 |
rs149291679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922331 | TCACCTTACCTTTTT[C/T]ATATCAGAAAATAAA | 5521 |
rs149296437 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825099 | CATTTAATGCAACTC[C/T]GCTGATATTTTAAAT | 5521 |
rs149305421 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041551 | TACGCAAAGTTCAGT[A/G]GTGCCATTTTTTTTT | 5521 |
rs149318777 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848447 | TTGAGGCTGTGGCAG[-/GT]TTTCTCAGACTTACC | 5521 |
rs149319225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671700 | TGTAAAAGGAGACAT[C/T]ATACATCCCAGAGAG | 5521 |
rs149324519 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962650 | AAAAATAAAAATAAT[-/A]AAAAAAAAAACAACC | 5521 |
rs149328241 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996100 | TCAGGACCAAGGACA[A/G]TAGGATGTGTGTACA | 5521 |
rs149330857 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813518 | TGTCGCTCGGTTCCA[C/T]GGAGACAAATCCAAG | 5521 |
rs149332902 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790740 | TGCCTCAGACACCTA[G/T]ATTTTCTTCTCTGAA | 5521 |
rs149352767 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808438 | TTCTGTGTTTCACTG[A/C]TTCTCAGTATTGAAA | 5521 |
rs149365204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986336 | CAATGTCCACAGAGG[G/T]TGTACTTAGACCTAT | 5521 |
rs149367325 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912298 | ATACCCTAAAGAGAG[A/T]GACCTTATCATCTGA | 5521 |
rs149370877 | in-del | -/TG/TGTGTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954756 | GAATATGTGTATATA[-/TG/TGTGTG]TGTGTGTGTGTGTGT | 5521 |
rs149374928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625108 | AGTAGCAGTTGATTA[C/T]CTTTACTTCATGGAC | 5521 |
rs149386663 | snp | C/G | 0.456685 | 0.140646 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013196 | TGTGAAGGACCTCTT[C/G]AAGGAGAACTACAAA | 5521 |
rs149392130 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766714 | TCTTAGCTTCTGGAA[C/G]AGTGAATGCTACCAC | 5521 |
rs149407209 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875607 | AAGAAAAATTCAGAA[A/C]TACATGTGAAGGAGA | 5521 |
rs149408784 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804486 | CCCTGCTCTGATCCA[C/T]TGCCTTTTAAATTGA | 5521 |
rs149415853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974040 | CGTGTTATTGATTTG[C/T]TTTTTCTAGAGAGTA | 5521 |
rs149430113 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592989 | TCTGACCCATTCCAC[A/G]CACACTCAAATTTAT | 5521 |
rs149435074 | in-del | -/T | 0.108755 | 0.206276 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980934 | TTAAACATTTTTTTT[-/T]AACCTAGATACTCAA | 5521 |
rs149436486 | in-del | -/TTCT | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590514 | ATAGATTCTTTTTGC[-/TTCT]TTCTTTGGCTCAGAA | 5521 |
rs149445262 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797976 | TCAGGTACAGGCTGA[G/T]AAATAGACAAACAAA | 5521 |
rs149447510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726851 | ATGCATAGAGGGCCA[C/T]ATACAGTTCTGGATT | 5521 |
rs149452942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962352 | AGAAAGAGAATGTGT[A/G]TGCATTAAAACCAGA | 5521 |
rs149453581 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893952 | TCGGGAGGCTGAGGC[A/T]TGAGAATTGCTTGAA | 5521 |
rs149460557 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904516 | CACAGGCAGTATTGG[A/G]AGCGTGTTCCCCGAG | 5521 |
rs149462594 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835381 | TTTGATTTCCCAATC[C/T]ACCACTTTATGAGGA | 5521 |
rs149464981 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618669 | AGGGAAGGCAGGCCA[C/G]AGCGGGCTGCTTCTG | 5521 |
rs149469760 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003798 | ATGATGTCCACCATA[A/G]CTCAGGGAAAGGAAG | 5521 |
rs149485447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598277 | CAGTTGATGACTTAT[G/T]TTTCCTTAAGACAGT | 5521 |
rs149496720 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682800 | GCACTAACAGCTCAC[A/G]ATCACAGAATCATCA | 5521 |
rs149497119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793230 | CAACTGAGGAAGGGA[A/C]AGTTGTAGGTGAAAA | 5521 |
rs149506440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958666 | CTTATCCTGAATTAC[A/G]TAGTTAATAAATACT | 5521 |
rs149509567 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860099 | TGGTTTCCTCTCAAG[A/G]TATCTAGCAGATTAA | 5521 |
rs149510524 | in-del | -/TAC | 0.00953873 | 0.0683987 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083368 | ATGTCTAGATATTTG[-/TAC]TACTTCAGAGAATTT | 5521 |
rs149517991 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083242 | TATGATTCTGGATGT[A/G]GATGCTGTTTCTATT | 5521 |
rs149529300 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918694 | TTTGGTTCTTCCTGT[G/T]TTTATACTTTGTCTT | 5521 |
rs149533629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633375 | TCCGATCACACACCT[C/T]GGCTGAACTGCGGTT | 5521 |
rs149537037 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070024 | TCAAACTCCTGACCT[C/T]GTGATCTGCCTGCCT | 5521 |
rs149540288 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037506 | CATTTATGTATTCAG[A/G]TTATTTGTTTCCTAA | 5521 |
rs149546659 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751952 | TGCTAGGGCAGAAGA[A/G]TGGCAGGAAATGGGG | 5521 |
rs149557852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990640 | ATAGGGGAAATGCTT[C/T]ATGAAATTGGAGTAG | 5521 |
rs149566262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777262 | TAAATAAAATGTGGC[A/G]CATATGTAAATGAAA | 5521 |
rs149580903 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881424 | TTATTTTATTTATTT[G/T]ATTTTTCTGAGCCAG | 5521 |
rs149581205 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947401 | AACAGGGACCAGCAC[A/G]TGACTGAAATCTGGT | 5521 |
rs149582325 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590397 | TTTGTTTTTTTTTTG[G/T]GTTTTTTTTTTTTTT | 5521 |
rs149584724 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666374 | GTATTATTTGACTGG[A/C]TGCTATAAACAAGCA | 5521 |
rs149586822 | snp | A/T | 0.0170251 | 0.090679 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056938 | GCTGCATTCAGAGGC[A/T]CAAGGAAATGATTTA | 5521 |
rs149603875 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731578 | TTGAAGTCAGATGGA[A/T]CTGAGGGTCAAAGCA | 5521 |
rs149605305 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651056 | AGAGACATTGTTCTA[A/T]TTTTTTTTTAAACAT | 5521 |
rs149608055 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621956 | GTACTTCCTCCCAGT[A/G]TACTCTAGCACTCCC | 5521 |
rs149616950 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839250 | ATGTGGCCGGGTGCA[A/G]TGGCTCCTACCTGTA | 5521 |
rs149620374 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770895 | TAGTTTACAGAGAAC[A/T]ACCTATTTACTTTCT | 5521 |
rs149622397 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009247 | AGCTTGGAGTGAACA[C/T]TGAATAGAATGTTTT | 5521 |
rs149627345 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935047 | CTTATATTAGTTTCT[A/C]GGCATTGAAGATTCA | 5521 |
rs149680191 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915009 | AAAATCAAGATGTTG[A/T]TTTTTCTCTTTTCTT | 5521 |
rs149681637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987678 | TACTACCAGACAAAA[C/T]AAACCCAAAAGAAGA | 5521 |
rs149690163 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888725 | ACCTCCCCTCCCACC[A/C]CCACCACTCCCTATA | 5521 |
rs149698342 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034781 | TACTTTATAGATAAG[A/T]TGTATGAGTTTTGGA | 5521 |
rs149700883 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818540 | AAGAAACATCACCAA[C/T]ATTCACCCCATTGTT | 5521 |
rs149709630 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053953 | GGCAAATGCCATTTT[C/T]CTTACCCATTGTCTT | 5521 |
rs149716406 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767898 | AACCTATTCACTCCT[C/G]CCTCTCCCCAAACCC | 5521 |
rs149719927 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806434 | CTTTAAGGTATTGCT[C/T]AGCTTGTAAAATGCC | 5521 |
rs149725682 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707405 | GGTTCAGCAGGCTCT[C/G]GTTGACTGGGACGGC | 5521 |
rs149731626 | snp | A/G | | | intron-variant, utr-variant-5-prime, synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878641 | CGGCTCCGGCAGGCG[A/G]GGGTAGGGAAGCTGG | 5521 |
rs149735188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983568 | CACTCTCCTGGGGGC[A/G]TCATTTTCCCAGTTC | 5521 |
rs149739473 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700248 | CTCAGAGGCAGGCAG[C/T]GGCAGATGGGAGAGC | 5521 |
rs149739920 | in-del | -/A | 0.0295035 | 0.117819 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608344 | ATGAACTTAGGAGTC[-/A]AGACATATTGGGGCT | 5521 |
rs149760634 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695398 | ATGAGGTAAAACAAT[A/G]TGTTTTTATGTCATA | 5521 |
rs149762928 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620432 | TCTCCAGCAGGCAGC[C/T]GTAAGGGAGGCGGCT | 5521 |
rs149768861 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799360 | TTTACTTTTGGTTAA[A/G]TGCCAGTGCTGTAAG | 5521 |
rs149771137 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728865 | CCATATAAGTCCAAT[C/T]AAACCTCTTTTTATT | 5521 |
rs149772442 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836994 | GGTGCTACGCCAACA[A/T]CTAGCAGCACCAATA | 5521 |
rs149778289 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740073 | ACAATGATTGCAAAG[C/T]ACAATAAATGGGGAT | 5521 |
rs149781706 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006210 | ACTCTTGTAGAAGCA[C/G]AGTTAGGAAAATTGC | 5521 |
rs149803881 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963109 | GTATAAAGTGAGCTA[C/T]ACCTCAAGCTCTTTG | 5521 |
rs149807872 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685397 | AACTGCGCCCCAAGC[A/C]TGTCACTAAGAAAGG | 5521 |
rs149820551 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863014 | GCTGAAGTACAATAC[A/G]ATAATCAGACTGCTT | 5521 |
rs149824613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795705 | AAGCATGTGAGGTGA[C/T]AGATAATTAGCTTGA | 5521 |
rs149841534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920174 | TGGGTTTCTGAAAAG[A/G]TGGCTGGGCAGAAAA | 5521 |
rs149842595 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848904 | ATGAATTTATGCATA[C/T]TGATTTTATACTTTG | 5521 |
rs149845518 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634706 | TGGCTGCAGAGCTTG[C/G]GACTTGTCAGCCTTC | 5521 |
rs149853292 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039376 | AGAGCCTGATCTCTG[A/C]CTGTACATCACAGAG | 5521 |
rs149858152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960279 | TATCTGGTTACATGT[A/G]TAAAGAAAAGACATA | 5521 |
rs149861157 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753571 | ATTGATATTACAGGG[A/T]GGGAGATTCTTGCCA | 5521 |
rs149865064 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646729 | AAATTAGCAGAATAA[A/G]AGCTACCATTCTAAT | 5521 |
rs149884226 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672941 | CTGAGATATGACACC[A/G]AATATAGGGAGGCAT | 5521 |
rs149894211 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949500 | TTATAATGGTTTTTA[C/T]CCAGACAGGCAATAA | 5521 |
rs149897754 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851513 | GTAAGTGATCCAAAT[A/G]CCTCACTGGGATAAC | 5521 |
rs149899040 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669682 | ACTGTCCCCTGTATG[C/G]TTTACATACGTTACC | 5521 |
rs149904069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060570 | GAGGTTGAGGCTGCC[A/G]TGATCCACGTTCACA | 5521 |
rs149906180 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074830 | TCATTAGAAAGCAGA[A/G]TCGATAGAGTACCTC | 5521 |
rs149910662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992861 | GTAGATAATATTATA[C/T]GTAGGATCAAGAAAA | 5521 |
rs149912206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788115 | CATGCCGTTGTGTGA[A/G]CATTTGCGCAAGTTG | 5521 |
rs149921332 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623903 | CAGTTACTGATGCTA[C/T]CTACTGAGCTGTCAA | 5521 |
rs149932609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840600 | CCAAAGGGGTTTGGA[A/G]GTCCATCAGCTGTGA | 5521 |
rs149939920 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010823 | TCCATATCCAGTTGG[C/T]TCACACATCTGGCCA | 5521 |
rs149944445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944206 | GACGTCTAAATTGCC[A/G]ATTGCCACTACATAT | 5521 |
rs149947027 | in-del | -/TCTTG | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911087 | TCTGTTAGACACTTT[-/TCTTG]CTTTTTTTTTTTTTG | 5521 |
rs149952945 | in-del | -/TATATATATATATACTGTATATATATACAGTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812481 | CTCTAGTGATAGCAG[lengthTooLong]TATATATATATACTG | 5521 |
rs149955363 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021319 | TAGCTGAGGAGACAG[A/G]GATGATTTCAGGCAG | 5521 |
rs149965705 | in-del | -/AT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079446 | ATTTTATATATATAC[-/AT]ATATATATATATATA | 5521 |
rs149974074 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654778 | CCATGGTCACCCTTC[C/T]GGGGTTGCTTGCACA | 5521 |
rs149974844 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049441 | GCATCTGATTGGAAA[G/T]GTTGGCTAGGAAGTT | 5521 |
rs149978859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831572 | GGCACACATTTACCT[A/G]TGTAACAAACCTGCA | 5521 |
rs149983207 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762936 | CCAACATCTGACTAC[A/G]GTCACTTTGAGTTCT | 5521 |
rs149994917 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873481 | TTGTGGTCAACAAGG[C/G]TTGATATGATCTGGT | 5521 |
rs149995987 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939939 | TTTGGCTTGTCATTG[C/T]TTTTTGTCAGCTCTG | 5521 |
rs150013230 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927038 | TACTGGTCATCATGG[C/T]TTGCTGTACCTTGGC | 5521 |
rs150033652 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826467 | GATAAGGGAAAATTT[G/T]CTTTGTGAATCTAAC | 5521 |
rs150062369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604400 | CTTGGCTTGGCATGA[A/C]AGTAGAGAATCTGCT | 5521 |
rs150066687 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997589 | AGTTGATCTTGATGC[A/G]TGCCAACATGTGAGA | 5521 |
rs150069743 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791542 | CAATGAGAGTTAGGT[C/T]CAGATTTTCACTGCT | 5521 |
rs150070863 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717709 | AGAACACTTTGTGAA[C/T]GGGCCCTTTCCTCCC | 5521 |
rs150076354 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621056 | TGCAGAGCAAGGTGA[A/G]CAGTTCACAGCTGAG | 5521 |
rs150080805 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008759 | GGGTTTCTATTCCCA[C/T]ACATCATCTTTGATA | 5521 |
rs150084097 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800511 | ATTACTTCACAGCTC[A/T]GACTTGCTCTCATAG | 5521 |
rs150086106 | in-del | -/GTTT | 0.328148 | 0.237472 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848139 | GTTTCTTATTCTTTA[-/GTTT]TTTTTATCTTATTAA | 5521 |
rs150087552 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696945 | TTGACAAGTTGCCCA[A/T]ACTGCACAAAAATTA | 5521 |
rs150095620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907373 | GAGCTTCTTCAGGAC[A/T]TTGGTTAAAATGAAT | 5521 |
rs150096994 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981068 | TTCTTACTCATTTTT[G/T]TTTGTTTGTTTATTG | 5521 |
rs150107073 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761657 | AGAAAATATTTGAGG[A/G]TTGTAACTGTCTGGA | 5521 |
rs150128042 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693846 | TCTGCCATAATAACA[C/T]GTTGCTCTGACAGCT | 5521 |
rs150135462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864135 | CATGCCATTATTTAT[C/G]TATTTCACAATTATT | 5521 |
rs150150420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976669 | TAGATGTTCTATTCT[A/G]TTCCATTGAGCTATT | 5521 |
rs150158442 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824970 | TCAAGTGATCCACCC[A/G]CCTTAGCCTCCCCAA | 5521 |
rs150160292 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756413 | ATGCTAGCTTCCTCA[A/G]CCTGGGAAAGAATAC | 5521 |
rs150164473 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921663 | CTCAAAATGGAGAAG[A/C]AATTTCATCTTCCTG | 5521 |
rs150167590 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961652 | TGATGCCTTTTATAT[A/G]TTAAGAGTATTAACC | 5521 |
rs150172868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932420 | GTGTGGTTACCCCTA[C/T]ACTGCTGTTCTTGTG | 5521 |
rs150176902 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648276 | GCTGCAAATGAAAGA[A/G]GCCCGAGTTTCTGAA | 5521 |
rs150177740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041134 | ACTAATTCTCTGTGT[C/G]GTTTTGGGAAGCTCA | 5521 |
rs150197216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675563 | GATGAAACATATAGC[A/G]AGTGCAATATTAAGC | 5521 |
rs150207790 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854497 | ACAGTCACTGTACTC[C/T]GCTATCAAACATTAG | 5521 |
rs150212505 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789907 | ATGGTCAGGCAGGCA[A/G]GGGCCAGATCAGGGA | 5521 |
rs150213801 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031702 | TTATACTTAGGCACA[G/T]AGACCAATGGAAAAG | 5521 |
rs150215887 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063776 | ATATTTCTTCTTGGA[A/C]AGATGAGAATGTTAG | 5521 |
rs150216115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952720 | AGAAAGGCAGTAACA[C/T]CATCTGTATAGTCTG | 5521 |
rs150223941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895916 | CAAAATATGTCCTGT[C/T]ACAGACCAGTCCGTG | 5521 |
rs150233233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624950 | TGAAACATTTTCACT[A/G]AATCTCAATCTTATT | 5521 |
rs150241846 | snp | A/C | 0.00126765 | 0.0251439 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590094 | TCTCCGCTTGCCCCC[A/C]ACACACACTTTTCGG | 5521 |
rs150248136 | snp | A/G/T | 0.00239401 | 0.0345304 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747968 | AGCATGGTTTAACCC[A/G/T]AGATGTTCCAGGGCT | 5521 |
rs150249928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670883 | ACACATGGAAAACCA[C/G]TTTTCTATGAATTGT | 5521 |
rs150255514 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842962 | GGGAGGCCGAGGCGG[A/G]TGGATCACCTCAGGT | 5521 |
rs150270047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023322 | ATGCCAAAAATAATT[A/G]ATATGAATGAAGTCA | 5521 |
rs150284358 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657724 | TCAAGGCCCCATAGA[C/T]GACCCCATCCCCAGC | 5521 |
rs150289334 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051311 | CATGGAGACAATGGC[A/G]TTTAATAAGACTGTT | 5521 |
rs150291562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833719 | GTCTCTTCTTTTTCT[A/G]TCTCTCTCCCCCTGC | 5521 |
rs150292515 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765557 | GGTAACATCTAAATT[G/T]CCACTCTAAATTATA | 5521 |
rs150299787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779769 | ATGAAGGTTTTCAGA[A/T]GCTGAAAACATTTAA | 5521 |
rs150316003 | in-del | -/GA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643183 | ATTACACACACACAC[-/GA]GAGAGAGAGAGAGAG | 5521 |
rs150316559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726319 | GCCAAACTAGATATG[A/G]CTGTCCTAGGTGCTG | 5521 |
rs150325960 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003331 | CCGGGCTATAGGTTA[C/T]GTCCCCTTCAAGCTG | 5521 |
rs150334024 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617839 | AGCTGGGATTACAGA[C/T]GTGTGCCACCACGCC | 5521 |
rs150343507 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827643 | ATAGAATCCACATTC[C/T]AACAAAATGAGAAAA | 5521 |
rs150349954 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733910 | TAGTAATAGTAGACA[A/G]TAATAACGGCAGTAG | 5521 |
rs150357041 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936345 | TAAGAAGATGCCTAA[A/G]TGATCATCCCACTCC | 5521 |
rs150364646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890332 | CACGGCTGTAGAGGT[C/T]AGGTTGGAAGCCTTT | 5521 |
rs150367036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793093 | TGATGAAAAAAGATT[A/G]GATTCTGGGTAGATT | 5521 |
rs150368628 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653648 | GATTTCTTGTGGCTG[G/T]GGCGACATGGGAGGG | 5521 |
rs150375639 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958455 | ATTAGTGTTAGTCAT[C/T]TTACCTCTGTAACCT | 5521 |
rs150383354 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718854 | AGTTCATTAGAGGCT[A/G]AGCCAGCTTCTAGGG | 5521 |
rs150387433 | snp | G/T | 0.0115144 | 0.0749975 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083153 | GATCTGAGACACATC[G/T]GTCTTAGGGAACATT | 5521 |
rs150387455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607437 | GCTTAACCCTTGCAG[A/T]TTGCTTTTCATATAG | 5521 |
rs150404543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713121 | TTCAGGGAGGCTGCA[A/G]TTTCAATAGGGTGGT | 5521 |
rs150407376 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636530 | GTTTTGCCTTTGCTG[A/G]TAGGTTGGGCCAACC | 5521 |
rs150418937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893362 | ACAGATTAATAAATG[C/T]ATGGATTAAGAAACC | 5521 |
rs150419715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820541 | TGCAATATAAAAGAG[A/C]AATGTGATCACAAAA | 5521 |
rs150427174 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916793 | TAGTAAGAAAAAAAG[C/T]TGGGCACTGAATTAA | 5521 |
rs150427892 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990134 | ATTGGAAGTATTAAT[A/G]TTGTTAAAATGTCCA | 5521 |
rs150431057 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036581 | TTCTAAGACTTTGAG[A/G]AATTGCCACACTGTC | 5521 |
rs150455589 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666209 | CTGAGTAATATGTCT[A/G]GTGTGATCTCAGTTT | 5521 |
rs150456356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785025 | GAGAATAAAGTACAA[C/T]CGTAGCACTCCATTT | 5521 |
rs150464755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880687 | ATCAGGTAGGCCCAG[A/G]CTCATTGGCCAGGCT | 5521 |
rs150468718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808130 | ATTCTCACTCCACCT[C/T]TGTGTCCTCACATCA | 5521 |
rs150524759 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791110 | TTTTAGGACCTGTTT[C/G]TCTTCTTGTGTCCTT | 5521 |
rs150530607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955848 | CAGTGGCATGATCTC[A/G]TCTCACTGCAGTCTC | 5521 |
rs150539157 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964968 | GTAAAATGAAGATAA[G/T]ATACCATTTGTCTCT | 5521 |
rs150543071 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687106 | AGGAAGAGAGGGAGA[A/G]GGAGAGAGAGGGAGC | 5521 |
rs150548719 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080100 | AGGAATTATAGCAAG[A/G]TTTTAAATAAACTGC | 5521 |
rs150553271 | snp | A/G | 0.0267878 | 0.112589 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914255 | TTTCCCGTTAAAGAA[A/G]ACCTTCTATTATGAG | 5521 |
rs150561118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629192 | GTCTGCCAGACTTCT[C/T]TAATTGGATGAATCA | 5521 |
rs150564659 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672578 | TACCAGATTAAAGTT[A/G]CATTATCTATCCCAA | 5521 |
rs150574354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749568 | AGAACTCTTTGCTTA[G/T]CCTAGATCCTGAAGA | 5521 |
rs150575903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850891 | GTCTGAAAAATGACC[A/C]CGCAATCTATCCATA | 5521 |
rs150585299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026027 | CTTTCATACATTGCT[A/G]GTGAGAATGTAAAAT | 5521 |
rs150605074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052812 | GTGGTAAGATAATCA[C/T]ATTTTTAAAAATTAT | 5521 |
rs150605978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944034 | CTGTCAGTAACTTGC[C/T]ATTTAGCTACAGAGA | 5521 |
rs150611711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739868 | ATTTTAATGAATAAT[A/G]TCTGTGGGAATCCTT | 5521 |
rs150612781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660202 | GGGTAATTCAGTGTA[A/G]CAAACCAAATAGAGT | 5521 |
rs150619034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069725 | ACAGAAAAGCCATCT[A/G]ATAATGTAGCATTCC | 5521 |
rs150626107 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847450 | CCATTACTCTCCTTT[G/T]ATCTGGTCAACTTCT | 5521 |
rs150627852 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781940 | TGGGGCCTGGTGAGA[A/G]GTGATAGGATCATGG | 5521 |
rs150644988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836477 | AACTGGACTCCACTT[A/G]TATTTTGTAAAGTTG | 5521 |
rs150649160 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620239 | GTTTGGCTTAGGGTT[C/T]GCCTGTCAATCTAAA | 5521 |
rs150658936 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938940 | CGCATGCTGCCACAC[C/G]TGGCTAATTTTTTGT | 5521 |
rs150663168 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736044 | GGGACCAGGTGGAGA[C/T]AATTGAATCATGGGA | 5521 |
rs150682544 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795391 | CCATTTGTGACCACA[A/T]GGAAGAACCTAATAC | 5521 |
rs150694283 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901847 | AGAAGGAAATGGAAT[A/T]GTAGTGCAAACACCT | 5521 |
rs150699271 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830367 | TCAATCGTAGTCATA[C/T]CCACTCAATAAGGTT | 5521 |
rs150701659 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608939 | CCTTCTATGAGGCCA[A/G]TATTACCCTGATACC | 5521 |
rs150703007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001513 | TGGACACATCTGAAC[A/G]TCAGAGGAACAAACT | 5521 |
rs150731144 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716454 | GTAAAATCTGAACCT[C/T]TCTCTAATAATACAA | 5521 |
rs150732278 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821442 | AGCTAAGCATGGCTC[A/T]CCCTTCTCTGGTTGT | 5521 |
rs150744140 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893938 | CTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAT | 5521 |
rs150746019 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928411 | GGCCTCTTCCACCTA[C/T]AGGCTTTTTCCATCT | 5521 |
rs150753720 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645564 | AGAATCCCACTGAAT[C/T]AAAAGGAAGCTGCTG | 5521 |
rs150771747 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710572 | TCCAGTGGGAAATTG[A/G]TAGCAGTCCAGACTT | 5521 |
rs150776601 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598034 | CTTCCTTCAGCCAGA[A/G]TCCCATTTCAGCTAC | 5521 |
rs150779336 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881981 | TTACCAAGCAATTAT[A/G]TAAAGAATTATTCTG | 5521 |
rs150782127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787685 | TGATTATCTTGCCTC[A/G]GCCTCCTGAGTACCT | 5521 |
rs150791618 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986814 | ATTGCCCTTAAAGTC[A/G]GAGTAGAAAAAGAGA | 5521 |
rs150817934 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982729 | GTTGTGTGGTACATA[G/T]GCACTTAGGATTGTT | 5521 |
rs150821801 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699797 | GTCCACCTTAACAAT[A/G]CATTTATAAGAGTGT | 5521 |
rs150824089 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623185 | CACAAAAGATTCTCA[A/G]TAAACAGAAACTGAA | 5521 |
rs150832974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909117 | AGGTCACAGAAAGTA[G/T]CAGGGTGAGTGACCT | 5521 |
rs150835365 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813163 | TATATGTATATATGC[C/T]ATATGTAGAGTATGA | 5521 |
rs150856111 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872799 | GGTTATTTATGCTTA[C/T]CAAGGCCCTATTCTA | 5521 |
rs150868635 | snp | A/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978103 | CCTCATTCTGGTTTC[A/G/T]GTTTGCACTTCTCTA | 5521 |
rs150874046 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770815 | CTGAGTGCCTTTGGG[A/G]GCCAAGAAATAGCTC | 5521 |
rs150876269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695161 | GTTACAAAAGAGTTT[G/T]CAGAATATATCATAT | 5521 |
rs150891837 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826226 | AATATCCTGCCCAAC[A/C/G]TAATAAAGGGTGGCA | 5521 |
rs150893733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758183 | TACTCATACAAGCAT[C/T]CTCCTTGGCTTAGAG | 5521 |
rs150900078 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996856 | TCACTCCATGTCCCA[C/T]CAGGCCTCACACTCC | 5521 |
rs150912610 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650075 | TACTTCAATGAGGTA[A/G]AAAATGTAATACTAT | 5521 |
rs150916725 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043399 | TTGCAAGAAGAGAAA[C/T]GCAGAGAAAAGACCA | 5521 |
rs150919750 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945591 | CTATAGCAGCTGCTG[A/C]TGATGTTTTTTAAGG | 5521 |
rs150919922 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023102 | TGCCATATGTACATA[C/T]ATTATATTTAGACAC | 5521 |
rs150926436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663588 | TGGTTTCCCAGTGTA[C/T]ATAAAGTTATGCTTA | 5521 |
rs150932574 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678136 | AACATTGATGCAAAA[A/G]TCCTCAATAAAATAC | 5521 |
rs150937722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071579 | CCTTGCCTCAGGGCA[A/G]TTGTACTGGCTGTTC | 5521 |
rs150938921 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848731 | TACTCTGCACCCTTA[A/G]AAAGAAGTCATGATG | 5521 |
rs150949994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620913 | AAGCTGGTTGCCATG[G/T]CACCGCAGAGGCCAG | 5521 |
rs150963145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742361 | CCAACACTCTGGATG[A/G]CTAGGGTTTAACTAA | 5521 |
rs150968804 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907092 | CGCAGGATGCCATTC[C/T]GACAGGGAAGTAGGA | 5521 |
rs150973674 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016948 | CCTACATGTCATGCT[C/G]TAGAGCTCCATTTTG | 5521 |
rs150977600 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738003 | CTGGGGACTATGTTC[A/G]ACCTTGAAGGTACAA | 5521 |
rs150981315 | snp | C/T | 0.000725032 | 0.019026 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638334 | CTGTACACGAAGGTG[C/T]TGCAATGATGGGGGT | 5521 |
rs150990597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844885 | AGCCTACACAGTGAC[C/T]TGAGGTCAAGGCAGT | 5521 |
rs151002855 | snp | C/T | 0.0283406 | 0.115616 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616951 | CACTGTTCACAATAG[C/T]CAAGATTTGGAAGCA | 5521 |
rs151008537 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797251 | TCTGTGGATTCTTGT[C/G]ATCACATAAAGCAAA | 5521 |
rs151012066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903528 | AGCCTCCTGAGTAGC[A/C]GGGACTATAGGTGCA | 5521 |
rs151013796 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806151 | GGGAGACAGTGTGTG[C/T]GATGCGCACATACAC | 5521 |
rs151017998 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002696 | GTTTCTGCTGCTGCG[C/T]CGGTGGGCGCAACTC | 5521 |
rs151022633 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976294 | AGGCATGCACCACTA[C/T]GCCCAACTAATTTTT | 5521 |
rs151028151 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705631 | TGGGTCCTGGATCAC[A/G]GTCCAAAGTCAGCAT | 5521 |
rs151038359 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606977 | TCTACAGGGAAGCAC[A/G]GCTGGCACGTTCTTC | 5521 |
rs151039728 | in-del | -/AGAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745205 | GAGAGAGAGAGAGAG[-/AGAA]AGAGACTATAAGCAT | 5521 |
rs151053757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728693 | GGGACTGGTCTTTCC[C/T]GTGCTATTCTCATGA | 5521 |
rs151061549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895565 | GTTTGTTTCATCACC[A/G]TGTACATGCATAGTA | 5521 |
rs151062652 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823527 | CGGCACACCACATAA[C/T]GAGCAGAACGTGCAC | 5521 |
rs151065117 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931219 | GCAAGTGGTAATGTG[A/G]TGAAAATGTTTTAGG | 5521 |
rs151090353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684866 | TTAGAGTCCAACTCA[A/C]ACCTTCTAAACCAGC | 5521 |
rs151090569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076869 | GACAGTACCCTGGAT[A/G]TAGTAAGCACTCACT | 5521 |
rs151093387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994322 | GCTGAGTCAGGAGGG[A/G]ACTCAGTCATTCAAC | 5521 |
rs151099474 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789471 | CTCTGGAGCAGTCTC[A/C]GGTGAAACAGCCAAA | 5521 |
rs151100881 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711968 | AATAAATCTCTTTTA[C/T]TTCTCTAAAGGACAA | 5521 |
rs151110059 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959634 | AGACAGAGAGGACAA[C/T]GGAAAGGTTTCTGGG | 5521 |
rs151113987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892649 | TGCCTAGTGTAAAGT[C/T]TCCTAAATCCAATGG | 5521 |
rs151135178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888311 | CTAATTCTGCCCCAC[A/G]ATACCCTGCCCCACC | 5521 |
rs151135634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911716 | ATACCTCTTCCCTCT[A/G]TATGGCCACACCTAG | 5521 |
rs151138147 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701953 | GTAAATTACCTATGA[C/T]TGGATTTATTAGGGC | 5521 |
rs151145590 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638120 | TATAAAATACGGAGC[C/T]GACTCCCACTTGTAG | 5521 |
rs151147283 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030357 | ACCTTGCAAAATCAC[A/C]TGTTGATTCTAATAG | 5521 |
rs151152382 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816177 | TGGATGCTGAGGCAG[A/G]AGGCTCGCTTGAGCC | 5521 |
rs151160886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657537 | GTTATGGAAGGAGCA[G/T]CCACATTCTCCTTCC | 5521 |
rs151170345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874249 | GAGGACAGAGACCAC[A/G]TCTGTATTGGAACAT | 5521 |
rs151175469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779491 | TTAAATGACTGCCGG[C/T]CCGGTGATAAGGCCG | 5521 |
rs151184720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059454 | TCATCACAGATAAGA[A/G]CAGGGTCACCAGGAG | 5521 |
rs151210081 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760128 | TGTAACACACAGTAA[A/G]CACGAATAAATTCAG | 5521 |
rs151211930 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733270 | GTACAGGGCTGGGTG[C/G]TCAAAAAACAGTGGC | 5521 |
rs151214240 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652204 | GGCTATGAGGTCTGG[A/G]CAACTAACCTGCTCC | 5521 |
rs151222231 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869726 | TTTACTTATCATGCT[C/T]GAATCCTTTTAAGTA | 5521 |
rs151226270 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840216 | ATTGCTGCCTGATTG[A/C]GTTCCCTTGAATATA | 5521 |
rs151227263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773993 | TCAGCCACAGAAGGA[A/C]ATAAAATATCTTAGT | 5521 |
rs151231235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045975 | AGCTCTCCTGATCTT[C/T]GTGTGCATAATAAAG | 5521 |
rs151232913 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936296 | TCATTGTGCCCATCC[A/G]TTATTACACTTTGTC | 5521 |
rs151264496 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762638 | TCTCCATATATCCAG[A/G]GTCAGGCACAGAACT | 5521 |
rs151265356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689494 | CCGAGGACCAACAGG[C/T]AATGTAGTCTAGGTA | 5521 |
rs151268298 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926417 | TTTTTGTTTTCGAGA[C/T]GGAGTCTTGCTGTGT | 5521 |
rs151271570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858810 | CCCTAGTGCTTTAAG[A/G]CTTGCACCACTGTCC | 5521 |
rs151275903 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665015 | AACAGATGTGCTCTA[-/C]TTCAGGCTTTGCTGT | 5521 |
rs151282621 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081545 | GAGAATGAGGCAGTT[C/T]GTTAAGGGGTGAGAG | 5521 |
rs151284744 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966180 | TTGGCTGCCTGCGAT[A/G]TTAGTGTTGGCCAGA | 5521 |
rs151285907 | in-del | -/TGTGTGTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049116 | GTGTGTGTGTGTGTG[-/TGTGTGTT]TGTGTGTGAGATATT | 5521 |
rs151294654 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708594 | TTCTTCCAAAAGAAG[A/T]AAAATTATGGGAATA | 5521 |
rs151301746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643473 | AGAAATTATGTCTCT[A/G]TATGTCCTAGATTGA | 5521 |
rs151306651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035884 | ATAAAAATATAATCA[C/T]GCTAAATCACTTCAC | 5521 |
rs151307454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820159 | GTGACTATAGTTAAC[A/G]ATAAGATATTGTAAT | 5521 |
rs151310926 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750998 | AGTAGGAGCTGAAGA[A/G]CATGCAGGGGGATCC | 5521 |
rs151320984 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923067 | AGCCATGTAATCAAG[C/G]CTTGCTCCAAAGCTT | 5521 |
rs180673323 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861347 | AGGTGTGAGCCACCG[C/T]GCCCAGCCTAATTTC | 5521 |
rs180680406 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876028 | TTCATACCTTCTCTA[A/G]GATCAGATTTTAAAA | 5521 |
rs180698049 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891588 | GTATATTCATTCAAC[A/C/G]TCAAATTTTTATTAC | 5521 |
rs180703153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845007 | CCATGAGATCCCACT[C/T]TTGGCCACTTCTTCA | 5521 |
rs180708492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853379 | ATCCTGCTCATCTCT[A/C]TATCAGCTTATGAAA | 5521 |
rs180713276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868325 | CACCAGAACCTTCTT[C/G]CCAGAAGGATGATTT | 5521 |
rs180715479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828811 | ATCACTGTTTCTGAT[A/G]TTCAAATAACTCCTT | 5521 |
rs180717473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808582 | GGGAGTCCTAAAACT[A/T]GACCCTGACTTCAAG | 5521 |
rs180719132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822861 | ATAAGTCTTTCCGTG[A/C]CTTTGTCATCTAGAT | 5521 |
rs180727883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781731 | TCATAGTTGTCCCAA[C/T]GTGATACTTTATGAA | 5521 |
rs180732410 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771965 | ATTCTATTTCAAAAA[A/G]GCCACCTTACTGAAA | 5521 |
rs180739771 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836095 | TAAATATTACTTTAT[C/T]TTATCATTTTGCTAA | 5521 |
rs180741860 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815728 | TCCCCACTTTTCCAC[A/T]CACACACACTTTAGG | 5521 |
rs180744582 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802185 | TAGTCCCAGTTTCAC[A/G]CCCCCTTTTCTCGCA | 5521 |
rs180750399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788907 | AGACCTTAGCATCAG[A/C]AAATCAATCTTGCTC | 5521 |
rs180752652 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738179 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 5521 |
rs180756118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695590 | TTCCCCATGGTTGGG[C/T]TGCCTGGAGTCATTC | 5521 |
rs180758256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713356 | GTCTTGTATAACACA[A/G]CAAGGACTCTCTTAC | 5521 |
rs180763355 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763973 | CTCAAACTATCTTCT[C/T]GCCTTGGCCTCCCAA | 5521 |
rs180763807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755658 | TTATATATTAATGCA[C/G]TGTGGTTTCATCAAA | 5521 |
rs180766572 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731663 | TCAATTTCCTTCTCT[A/G]TAAAACAGTGAAGAA | 5521 |
rs180769349 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722578 | TACAAAGAATAAGAA[A/C]AACAGCTTCATCTAA | 5521 |
rs180774483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660990 | TATTGTTTCATGAGA[A/G]AAAGAAATAGGGGCT | 5521 |
rs180782809 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747899 | TGAAAAAAATTAGGA[C/T]GATACGAAGGGTGAT | 5521 |
rs180800731 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704734 | GCTGAGTTTATTATT[A/T]TTTTTTTAAATCAAT | 5521 |
rs180821816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639033 | ACTCTATATAATTAG[C/T]GTTTTCCTTATCCTC | 5521 |
rs180824717 | snp | A/C | 0.0599851 | 0.162463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077310 | CACACACACACACAC[A/C]CCCACACCCACACCC | 5521 |
rs180825662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686022 | GAGCTGTAGAGAATA[A/G]GATGAAAAACATCAG | 5521 |
rs180833665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013260 | AAATGGAAGAACATT[A/C]CATGCTCATGGGTAG | 5521 |
rs180839268 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602815 | TGACCCAATGTCTTA[A/G]TCTCTGCCCTCAGCT | 5521 |
rs180841962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041767 | TATTCATTTGTTTAA[A/C]CCTTTTCTACCATAG | 5521 |
rs180843779 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051607 | AGTCACAGTACCCTT[C/G]TCCCTTTAGGAAAAG | 5521 |
rs180846163 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653149 | AGGCTAAGTCACTGG[C/T]CCAGGGTTGCCCAGC | 5521 |
rs180855220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057118 | CTGGTCTCCCCAGGA[A/G]GGAAAAAACAAAGTC | 5521 |
rs180856551 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999041 | AAAAAAAAAAAAAGA[A/G]TCAATCTCTGGTTTT | 5521 |
rs180862218 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032716 | GCTGTGTAGTATTCC[A/G]TCTTATGTATATATA | 5521 |
rs180862512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146622756 | CTTCTATAGAGCAAG[G/T]TTCCCAAGTTGTGAT | 5521 |
rs180873162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067908 | TTTCTTCCACTTGCT[C/G]TGACATCGTGTCTGT | 5521 |
rs180883960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984485 | TTATCCATTCATCTG[C/T]TGATGGACACTTAGA | 5521 |
rs180891738 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976413 | AAGTGCTGGGATTGC[A/G]GGCAGAAGCCACCAT | 5521 |
rs180892959 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935896 | TCTCATCTTTCCCAG[A/C]AACTTAGGCAAGTTA | 5521 |
rs180896370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921034 | GTGCAGGGTACAGTA[C/T]GTTGTCTCTGGTCTT | 5521 |
rs180898304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945642 | CCACTGGAGAGGCAA[C/T]AGGAAATAAAAATAG | 5521 |
rs180898941 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954009 | ATCTACCAATTGGTA[A/T]CTGTGAGGTAGACTT | 5521 |
rs180899911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959984 | TGGAGGAGCCATTGA[C/T]AGGTTTTAAGCACGG | 5521 |
rs180907209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021983 | TGAAATCTATGAAAA[A/G]AATACCTAAAGGAAC | 5521 |
rs180915046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990047 | TGAAATATCTCTACA[A/G]TTAAAACCATAAAAC | 5521 |
rs180917962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003862 | CTATGGGAGGCCTTA[A/T]GAAAATATACTCCCC | 5521 |
rs180934750 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820809 | TCCTAGGACTCCATC[C/T]GTCAAATTGCCAACC | 5521 |
rs180939888 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904641 | TACAGACTGGCTGAA[A/G]ACATCTGCTTGAAGT | 5521 |
rs180950743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865227 | AAAGCAAACAAACAA[A/T]CCCTATAGATGATGT | 5521 |
rs180952777 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928280 | TAGGTTTATATATAT[A/T]TTTTTTTAGATCAGA | 5521 |
rs180954444 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967786 | GCAGTCCCAGCCTAC[A/G]GTTACTCTTCAATTA | 5521 |
rs180964791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895387 | TGTCTATGAATGTTT[A/G]TTTAGCAAAAGTTTC | 5521 |
rs180966571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768567 | TTTGCATCCTTTTTC[C/T]TCTTAACACAGAGTG | 5521 |
rs180971003 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805658 | CAGATGAGCCTGTAG[C/T]ACAAATTGCACCCTA | 5521 |
rs180978519 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735388 | ACAGAGAACCCTGAG[A/G]GGATTTGCAGAATGA | 5521 |
rs180986376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832638 | TTAGGAGATCCACCT[A/G]CCTCGGCCTCCCAAA | 5521 |
rs180988899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592660 | CTGGAATTTGCTGGT[A/G]GATAAGTGATCTTCA | 5521 |
rs180992142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880115 | ATGACATCTTCCTCA[C/T]CTCCAGAAATTGACT | 5521 |
rs180993612 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912008 | TTTGGGAGGCTGAGG[C/T]GGGCAGATTGCCTGA | 5521 |
rs180994164 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811286 | TACAGGCGTGAGCCA[C/T]GGCGTCCAGCCATAT | 5521 |
rs181002619 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752301 | GATACATTTATTGAG[A/G]TGAAAAAAAGCAGTG | 5521 |
rs181015623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699495 | TCCCCCATCATTCTA[C/T]GAATGAATCAGGCTT | 5521 |
rs181016458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850688 | TCTAGGTCCAATAAT[C/T]CTCTTATTACACACT | 5521 |
rs181028097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067325 | TCAACCTCCTCTTAC[C/T]CCAACCCCTAGTAAT | 5521 |
rs181044949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775406 | ATGTGATTGTCTCAA[C/T]TGACAAAGAAAAAGC | 5521 |
rs181045854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759606 | CTCTCCTTGCCTCCA[C/T]CTTCCAAGTTGAATT | 5521 |
rs181046580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631408 | CTTGCTGCATTCATG[A/G]TGAGATTATCATTTC | 5521 |
rs181053983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615566 | CTGAAAACAAATTCA[C/G]TAAAACTGCAGGATA | 5521 |
rs181053984 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652094 | GAAAGTCTTTGTGGT[C/T]CCCCATCCCAATTAC | 5521 |
rs181056724 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795509 | GAAACAGAGTAGAAG[C/G]GTGATTACCAGGGGT | 5521 |
rs181056992 | snp | A/G | | | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638260 | ACTCACATTTGGTGT[A/G]CCTGTCACACAGGGC | 5521 |
rs181066470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983824 | AGATTTCTTCTTTTA[C/T]AATTTTTTTTCTCTT | 5521 |
rs181066671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741725 | GGCCAGATTCTGATA[C/T]TGACAGTACACAATT | 5521 |
rs181067197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726461 | CACATACCCTGATTA[C/T]TAACAATAGTGACCA | 5521 |
rs181068062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998405 | CAATCTGGGAAGCCT[A/G]TGAAATTGCCAGCCC | 5521 |
rs181072008 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708328 | TGCCACTGCACTCAC[A/T]CCTGGGCGACAGAGC | 5521 |
rs181073471 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683612 | GTAGTTCCTTTGGCT[A/G]ACATGGAACTCAATT | 5521 |
rs181086277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665555 | ACCACTCAAACCTTC[C/T]CTATGTCAGCAAGAA | 5521 |
rs181090917 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678282 | TATAAACAGAGCCAA[A/T]GACAAAAACCACATG | 5521 |
rs181094048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051202 | AAGAGTACCAATTTC[A/G]GATTCAGAGAGTTTG | 5521 |
rs181096747 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012830 | TTCTGCCTTCATTTC[A/G]TTATGTACCCAGTAG | 5521 |
rs181100227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031759 | TACTTACAGTCAACT[A/G]ATCTTCCACAAAGCA | 5521 |
rs181100741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058287 | CCTATCATAAAGCTG[A/G]AATATATCATTCAAA | 5521 |
rs181101418 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660239 | AATGACTGTCAAATA[A/G]AATAAACCACTAACA | 5521 |
rs181102602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647423 | CCCAGAGGTGGCTAT[A/T]CTTCAGTGATGAGAG | 5521 |
rs181104394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022899 | AGGCAACATAAAGAA[C/G]TTTTCAAAAAAGAAA | 5521 |
rs181112139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042106 | CGCCCAAATCCCCAC[A/G]TCTATCACCTTGTAA | 5521 |
rs181120431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078368 | ATAATTGATGGGAAG[A/C]CAGTCACAACGACAA | 5521 |
rs181140571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621884 | CAGGTTGTACTTGGT[C/T]CTCATTTTGCACTTG | 5521 |
rs181147447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601357 | TATTCAGCACTTTGG[A/G]AGGCCTAGGCGGGAA | 5521 |
rs181154961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967437 | AATAGGTTCCATTGA[C/T]ATTATTCCTATTTTA | 5521 |
rs181170231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004676 | TGGAGAACGAGTTAC[C/T]CATTTGTTGTCCCCT | 5521 |
rs181191337 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911276 | TTTAGTAGAGACGGG[A/G]TTTCGCCATATCGGC | 5521 |
rs181195465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904101 | GTAGGCTAGTATTTG[C/T]AGAATGCAGACATCA | 5521 |
rs181212287 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872052 | TTCTTAAATGCAAAC[A/G]CCAAAGTCTAGGAAT | 5521 |
rs181214987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864797 | TATCTTTAAGAATTT[C/T]TTCTCTGATCTTCAC | 5521 |
rs181218308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826655 | AATGCATTCTGGTGG[C/T]GTTTTCAAAACTCAG | 5521 |
rs181219054 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887950 | GAATTAGGTATTCCA[A/T]TGTCTTTAACTCATA | 5521 |
rs181225899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934556 | GTTCTGAGGTGTCCT[A/G]GAGTTAGAAGAGGTA | 5521 |
rs181226265 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840964 | ATGAAACAAGACAAA[A/T]ATGTATTAAACATTA | 5521 |
rs181229242 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879145 | ACCCTTATATGATGC[A/C]TGTGGTCCCTTGGTG | 5521 |
rs181230952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953568 | TTTAAGTCACAAAAA[C/G]ATATAAAGTGATACA | 5521 |
rs181244381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698918 | GAGAATTAAACACAA[A/G]GGCAAGGGTCTGCAG | 5521 |
rs181244829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920855 | ATCTCATAGAATTCT[C/G]TTAGAAAATCATTCC | 5521 |
rs181245389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063134 | TTAAGTAATAAATAT[A/G]TAAATATTACAGAAG | 5521 |
rs181248211 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717748 | TATCCCCTGACCTCC[C/T]TCCTTACCATTTTCT | 5521 |
rs181248921 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857373 | GAAGCTTCAACATAC[A/C]ACTAATATAGAACAA | 5521 |
rs181254645 | snp | A/C/G | 0.00358891 | 0.0422285 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081797 | AATGTGGCCTATTTT[A/C/G]TTCCAAGGTTATTTT | 5521 |
rs181256759 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796742 | GTCTCTGTTCCCAGT[C/T]ACCACTGCCAAAAAC | 5521 |
rs181257431 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683182 | CATGTACCCTTCCTA[C/T]CCCGCCTTTTCCCAA | 5521 |
rs181259568 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820388 | AAAACCATGCTAGGT[A/T]AAATGGAGCAGCCAG | 5521 |
rs181261366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665287 | TAGTGTAGCCACCGC[C/T]ACCCATGATCTTAGC | 5521 |
rs181262113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895296 | CTGATGCAGACAAGT[C/T]GGCCCCCTGCCATAC | 5521 |
rs181263524 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649630 | CTTTTTTGTATTTTT[A/G]GTAAAGTTGGGGCCT | 5521 |
rs181272714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635375 | TTATTTCATCATCCA[G/T]GTATTAAGCCTAGTA | 5521 |
rs181275998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849856 | TGTATAATATCTTAA[C/T]ACATCCTCGAAGTTC | 5521 |
rs181278490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618377 | AGGAGCACAGCCCTG[A/C]TGACACCTTGACTTT | 5521 |
rs181278693 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812103 | ACTTTGGACTTTTGT[C/T]ACTAACTAGTTCTGT | 5521 |
rs181279237 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784955 | TGGAATATATGATTG[C/T]GAAGAAAAAAGCAAA | 5521 |
rs181281524 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995738 | GAGATAAAACATTCC[A/C]AAGAAGATATGAGTA | 5521 |
rs181290169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776959 | AGATACTACTTCACA[C/T]CTACTAAGATGGCTA | 5521 |
rs181293948 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760705 | TGTGGGTGAGGGATG[C/T]ATTGGAAATACCTGG | 5521 |
rs181294858 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981317 | TCCTCACAACTAGAA[A/G]TTTCTATTTTGTTTT | 5521 |
rs181298917 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027289 | TACTAAATACCACTG[A/C]ATTGTTCATCTGAAA | 5521 |
rs181311330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727506 | GTGAAATAATAAACA[C/T]TGGAGACTTCTAGAA | 5521 |
rs181311402 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045964 | TTCTTTAGGGAAGCT[C/G]TCCTGATCTTCGTGT | 5521 |
rs181311691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007670 | TGTAACACTCACTGC[A/G]AAGGTCTGTGGCTTC | 5521 |
rs181318972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751771 | TGGTGATTGCCCCCA[A/G]AGGGTGGGGGCAGGT | 5521 |
rs181335940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832273 | ACAATAATGTCCTTG[A/G]CCTTCACATTCACTC | 5521 |
rs181362414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851081 | TCGAAATGAATATTA[C/T]TCAATATTACATAGA | 5521 |
rs181369075 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598428 | TACTAATTGTCTAGA[A/T]GATCTCATCCAGTCC | 5521 |
rs181372070 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866063 | AGTTTCACTAGAATA[C/T]AGCCATGTCCACATA | 5521 |
rs181378894 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768187 | CAAGCAATCCTCCCA[C/T]CCCAGCCTCCCGAGT | 5521 |
rs181380998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880562 | AGACATTGTGCCTTC[A/G]GTTGGAATGATCTTA | 5521 |
rs181383104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920084 | GGTAAACTGCATAAT[A/G]TGTGGCACATAATCA | 5521 |
rs181385058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820986 | ATCTCTCACCAAGAT[C/T]AGTGCATCGCCTTCT | 5521 |
rs181389041 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036980 | GCTCATTTAATTCCA[C/G/T]GTTAATCCTATACAG | 5521 |
rs181389159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742532 | TGATTTCTTCACCTC[C/T]CTACTTTTTTCTGTT | 5521 |
rs181392853 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940631 | CCTTTGATTTCCCAA[A/C]AAAATCCCTTTTCCT | 5521 |
rs181393454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805047 | CTCCTCCTCAAGCTG[C/T]GAGGTCAGATTTTAT | 5521 |
rs181393889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903557 | CATGCCACCACACCT[A/G]TCTAACTTTTAAATA | 5521 |
rs181394290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001979 | CCCTGCGGCCATGAG[C/T]GGAACTCTCAAAGTC | 5521 |
rs181395434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709752 | ACAGATGGGAGAATG[G/T]GACAATATCTTTGAT | 5521 |
rs181405746 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833156 | TTCTGAAATTTCCAC[A/C]TTAGCTCATCACTTC | 5521 |
rs181411148 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734312 | TCCTCCTGCCTTGGC[C/T]TCCCAATCTGCTGGG | 5521 |
rs181413596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923914 | AAGAAATGGTAGTTT[G/T]TTCCTTTGCAGGGAC | 5521 |
rs181417925 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908387 | ACACATATTCTACTA[C/G]TAAGTTCTTGGTGTT | 5521 |
rs181421856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070396 | AGGCGTAATCCTTAC[C/T]TGAAACCTTGAGCAA | 5521 |
rs181434558 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956623 | CATAGACTTGAGATT[A/G]TAGCTCTTTCCAGAA | 5521 |
rs181463479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970990 | GCATAGAAAAACAGA[G/T]ATCCCTTCGAAACAT | 5521 |
rs181495570 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018613 | AAATGTTGATGTAAC[A/G]ATGAGAAACCCAGCT | 5521 |
rs181503257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856830 | ACAGACAGAGAGCCA[C/T]GGTCTCAAAGTGTTG | 5521 |
rs181505647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759900 | TAGTAGTTATTGTGA[A/T]GTCTTACAGTTATAT | 5521 |
rs181506449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887383 | AGAAATAAATTTTTA[C/T]CTACTAGAAACTTGA | 5521 |
rs181515675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776465 | TTCAAAAGAATGAAG[C/T]TGGGCCCTACCCAAA | 5521 |
rs181517521 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964172 | AACATGAGATTCCAC[G/T]GCTAAATACGTCAGA | 5521 |
rs181521938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796141 | CATATAAAAATGTCA[C/T]TGCAATGATATGACA | 5521 |
rs181523402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726822 | TTCATAAATGCTCCT[A/G]GGGAATCATCAGGAT | 5521 |
rs181525546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606733 | CTGTCTGGGCTGCGA[A/C]ACAGACACATACTAG | 5521 |
rs181529462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826135 | ACTTCCTCGGTACTT[A/G]GCATTTCTTTTTTAA | 5521 |
rs181530937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054696 | GGGTTTTCAGAACAG[A/G]CTGGTCGCCAGCTCA | 5521 |
rs181531664 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592562 | ATGAACTACCAGGGC[A/C]GTTGGCCAGGTCTCC | 5521 |
rs181532874 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689886 | AGCTCAGAAGCAGCT[C/G]AACTGAAGACCATGT | 5521 |
rs181538750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635274 | AAATCACTCTAGTTT[G/T]TTTTTTTTTTAACTT | 5521 |
rs181539081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709266 | GTTTCCTACTTAACC[A/G]TAAGTGCAGTATTAA | 5521 |
rs181540003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675790 | GCAGCTCTTTTTTAT[G/T]GTTCTGCACTGTTAA | 5521 |
rs181545031 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617954 | CTGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 5521 |
rs181548625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657072 | TGACACCTAAGTGGG[A/G]GTTGGCGGGTCACAG | 5521 |
rs181550173 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597006 | TAGAATTTTGCTGTC[A/C]CTCCACATGCCAGTG | 5521 |
rs181558836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949345 | AAATTGACAAGAGTT[C/T]TGAATAGACATTTCT | 5521 |
rs181560393 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963907 | TAAAAAGAACAATTG[C/T]AACAGCTTGACCTTT | 5521 |
rs181568323 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932084 | TGTTTGAACTGAATC[A/G]TTTAGATTGGCCCAC | 5521 |
rs181569217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995451 | ACAGGCTCTGCCTTA[C/T]AAGAACTGATTCTCT | 5521 |
rs181577251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980743 | ATTTGAGGCTATATG[C/T]TGTCAATTTTTGGAA | 5521 |
rs181591918 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987295 | GACACATGTGCAACA[A/T]GACACATGTGCAACA | 5521 |
rs181592938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072644 | GTGGAATGAGATAAC[A/G]TGTTGAAAGCAGTTA | 5521 |
rs181598723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055429 | ATTTTCTAATTAGCT[A/G]TGTCAGCTTTGAGAT | 5521 |
rs181602481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917185 | GCAAAAGCAAGCTGC[A/T]TCATAGTTGCTCCTG | 5521 |
rs181608603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899932 | TTCCTGGAGGAAAAC[A/C]CAGGCCATATCTATG | 5521 |
rs181622454 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840461 | TAGTTTCTTTTCCTT[A/G]TCTTCAGAATAACCA | 5521 |
rs181641360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871596 | CCTCCCTGTGGGATA[A/C]TGGAAAAGGCCCAGA | 5521 |
rs181649691 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811803 | CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 5521 |
rs181663120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874848 | AATCAAACCATTGTG[C/T]TGACTTTATTTTTGT | 5521 |
rs181682041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697818 | TATTTATTGAGGGCC[G/T]AATCTGTGTGTGCCA | 5521 |
rs181682597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828457 | AATTGCATTAAGTGC[C/T]AAAGAATGTACTGCT | 5521 |
rs181686980 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844395 | TATATACTGAAACAT[C/T]CAAAATGCCAGACAA | 5521 |
rs181694583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664308 | TTGCTGCTTTATTAA[C/G]TTTATTAACACAGCT | 5521 |
rs181695206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861095 | TGAGTCTCCTCTGTC[A/G]CTCGGGCTGGAGTGC | 5521 |
rs181699141 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607484 | CAAACAGTTGTTTGA[C/T]AGTGACACTTTAACA | 5521 |
rs181700706 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045291 | GGTGATTCCATAAGA[A/T]TTTCAAATTGTATTT | 5521 |
rs181701389 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756730 | TGAGAATTAAATGAG[A/T]GAATTCATGTCGTGT | 5521 |
rs181703144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801077 | TGAAATAAGTCAGAT[A/G]CAGAATGACAAATAT | 5521 |
rs181704889 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081483 | ACTGGCCCTTTTCAC[A/G]GGAATACTAATGCTT | 5521 |
rs181707447 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781411 | TGAATATTCCATTTG[C/T]CTGTCTGATGCCAAC | 5521 |
rs181707831 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815363 | ACACACTTTCATTGT[A/T]TGCTTATTGAGAGCA | 5521 |
rs181734661 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763350 | GCTGGTTCAAATGCT[C/G]GTTGAGGATCTTCCG | 5521 |
rs181749676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006878 | TATGAGATGCCGCCC[A/G]GTGTTTACAGGAAAA | 5521 |
rs181770889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717154 | TAATTGTTCATTGCT[A/G]TAGGCTTATAGCCTG | 5521 |
rs181772563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037585 | TATGTGTGTGTAAAA[A/G]TATGTGTTGAGTGAG | 5521 |
rs181776217 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682592 | GCAAAATGGGAATAA[A/C]AGTAGTACCCACTCC | 5521 |
rs181778466 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675176 | CATGTTGGCCAGGAT[A/G]GTTTCAATCTCCTGA | 5521 |
rs181781593 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656791 | CGGATCACCACCTTC[A/G]CTGTGCGGGTGAGGA | 5521 |
rs181783460 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643370 | CTATATTCTAGTAGG[A/G]AACAGTCAATAAACA | 5521 |
rs181787111 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890642 | GGTTGTATATATTTT[A/C]AAACTCAATAAATAT | 5521 |
rs181788134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626471 | GGAAGATAATTTTTG[G/T]TTTTTGCAGGCAAAA | 5521 |
rs181800584 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955493 | TCCCCAGATAAATTG[A/G]AAGCACCTGAAGTAT | 5521 |
rs181801959 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837302 | GTAAGTTGTTCTGAG[A/C]CCATTTAAAGTAAGC | 5521 |
rs181805309 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649530 | GCTTACTGCAACCTC[C/T]GCCTCCTCAGTTCAA | 5521 |
rs181805891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916093 | AAAGAAAATAAAAAA[C/T]TGTATCACTTTGAAG | 5521 |
rs181807700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606908 | ACGATGAAAAAGGAA[C/T]GGGCTCGGAATCATG | 5521 |
rs181810865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971430 | TTTTAAAAACTTACG[C/T]TCTATGTTGGGAGTC | 5521 |
rs181811218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062334 | TTTCCCCATCATCAA[A/G]TGATGCATGACGGTA | 5521 |
rs181814473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869539 | AAGTGCAAATAAAAC[A/G]GGCAGTGTGTACTCA | 5521 |
rs181815442 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026808 | TTGCAAATGTTGGCC[A/G]TTATGTGGAGCAACT | 5521 |
rs181816054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899058 | AACCATTGTGGAAGT[A/C]AGTAGGGCGATTCCT | 5521 |
rs181816369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923529 | CTAATAAACAGATCA[C/G]CTTAGCCCAGCACGA | 5521 |
rs181820822 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957127 | AGTAAAACATATTGT[C/T]CAATATTTTACCACT | 5521 |
rs181825530 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809719 | GCTACTAAGAACAAC[A/G]GGAAATGATTGGAGG | 5521 |
rs181827139 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044953 | AAGAGCAAATTCACT[A/C]CTATGCCTGGAATGT | 5521 |
rs181829333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019073 | GTATTTATGACTACC[C/T]GAAGTGTTTCATTTG | 5521 |
rs181836190 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987779 | TTCTTACTACTATTT[A/G]TAATAACCTTGAATA | 5521 |
rs181836297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061125 | GCTATTAAATGCCAG[G/T]CACTCTTCTAGGTGT | 5521 |
rs181837704 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002380 | ATAAGTGAGGACAAA[A/T]GGCATCACTCTTCCA | 5521 |
rs181841392 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853597 | AACCCTAATTGAGTA[A/G]CTAATGCATGTAAAG | 5521 |
rs181855201 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883023 | TTCCTACACAGGAAA[C/G]TTTTGGGTCACCCTG | 5521 |
rs181863552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809115 | GATCCAATGTCAGGG[G/T]CTTTGGGGGCAGCTT | 5521 |
rs181866168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773185 | GGAATTTTAAATCAG[C/T]GTAAGGGATTAAACA | 5521 |
rs181868071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823197 | CCAGAGTTTACTTCT[C/T]CTTCTTCTTCTTTTT | 5521 |
rs181869627 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836712 | AGAAACAAGTCATTG[C/T]CAAAGTTCAGAGAGA | 5521 |
rs181872495 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746871 | TAAACTCCCATTATG[A/C]AGATACCAAAACTGA | 5521 |
rs181874109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942194 | TGAGTTAGGACTTTA[A/G]CATATTTTGGAGAGA | 5521 |
rs181894487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713034 | AATCATCAATGAACA[C/T]ATTAAATTACATTGT | 5521 |
rs181919053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055062 | GGAAATGGGGAAGGT[A/G]TAGAAGGCTCAGCCT | 5521 |
rs181922849 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035357 | GGGAAGGCCTCCCCC[A/T]TGATCCAATCACCTC | 5521 |
rs181934461 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618967 | TCTACAGTGACTCTG[G/T]GTGGCTGATAGCCAA | 5521 |
rs181947271 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746309 | CTTGACTAAACAACA[C/T]CTATCACTGGCGCAT | 5521 |
rs181958459 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763014 | AGTGACCTGTGACCC[A/G]CCTGGCTCCAAGAGC | 5521 |
rs181965731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077893 | CCTATCTTCAGTTCA[C/T]GTGTATTCATAATGA | 5521 |
rs181965846 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730378 | ACTTTGGACTGTGGA[C/T]TTTTGGGTTAATGCT | 5521 |
rs181970574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693676 | ATGGTGCCTCAGTTT[C/T]TTTATTTGTAAACTG | 5521 |
rs181972966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010495 | GGTGATGGGAGACAG[C/T]GACAGATTTTCAGGC | 5521 |
rs181974039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653343 | ATAATGGTAGTGGTA[C/T]TCATAGTAGTGTGGT | 5521 |
rs181975615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670604 | GAGTTCAAACAATTC[C/T]CTTGTTTTAGCCTTC | 5521 |
rs181976463 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712301 | GTATTTTGAAGAATA[C/T]TATAAAGTATGCTCT | 5521 |
rs181977009 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995218 | TTACTTTCAAGCTAT[A/T]TGTTTCCATAGTAAT | 5521 |
rs181985848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639960 | AACTTGATATAACTG[C/T]CCCATTAGACTGAGA | 5521 |
rs181985886 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678138 | CATTGATGCAAAAAT[C/T]CTCAATAAAATACTG | 5521 |
rs181987924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026302 | TAAAAAGATCGAACT[A/G]TTGCTACACACAGTA | 5521 |
rs181991564 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623073 | TGTCAGGGATGGCCC[C/T]TGGAATCTTCCGGTA | 5521 |
rs181996872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603000 | TCCAGAGGCAGTAAA[A/G]TGGATGGGCTTAGTA | 5521 |
rs181999626 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931189 | CAAGCCAGAACCTTC[C/T]GCAATAATACATTGG | 5521 |
rs182005758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966855 | ATCACCTCATTTAAT[C/T]TCTATAATCAGCCTG | 5521 |
rs182007347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953093 | GATACTCAGTTACAT[A/G]CCCTCCTGCTAATCA | 5521 |
rs182011242 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934440 | ATGGCCAGTGATGAT[A/C]AGCATTTTTTCATGT | 5521 |
rs182015299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897032 | TGTCATCTCCTTTTC[C/G]CAAGATCTCTTTAAA | 5521 |
rs182021959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963362 | TCTTCTTAGCACCAC[C/T]ACGGAGTAGGGATCT | 5521 |
rs182024096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997710 | TCAGTAATATAATGT[A/G]GTAAAATTTTTAGAA | 5521 |
rs182024244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041973 | TTTCACTGGCAGCCC[C/T]TTCCTCAAGGATTTA | 5521 |
rs182028188 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883730 | AGCAAGTTTGCAATT[C/G]CTGTTTGTGCATGCT | 5521 |
rs182033106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876642 | CTCTGTATAGGGGAG[A/G]GATGGGCTGCACATC | 5521 |
rs182034739 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907330 | ATGTGCATTTTCCTG[A/C]AGCTCAGCTCAAGCA | 5521 |
rs182036993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057759 | TGTGCTTAAGAGGAG[C/T]GAGGCTGCAGTTAGA | 5521 |
rs182039716 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909150 | ACTGTTTCTGACCAC[C/G]AGCTATTACCACAAC | 5521 |
rs182040666 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983337 | AGGCGTCCGCCACCA[C/T]GCCCGGCTAATTTTT | 5521 |
rs182061766 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940228 | CTTTGTCTTAATAGA[G/T]CTACAAGTCTCAGAG | 5521 |
rs182065936 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854232 | GAGCCCTACAAGGCT[C/T]CATGTCTTATACTGC | 5521 |
rs182086204 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790879 | AAATGAACTCTTGAG[A/G]AACAGTCAGACCTTC | 5521 |
rs182091937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823520 | ACTTAGACGGCACAC[C/T]ACATAACGAGCAGAA | 5521 |
rs182100311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838067 | TATGCCCCTGTCCTA[C/T]GGCGTTAAAGAAATC | 5521 |
rs182120468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792555 | GTATGTTAGAAGGTG[A/T]CTATGGGAAAGCAGA | 5521 |
rs182122069 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079010 | TTTTTCTTTCTTTTT[A/T]AAAAAAGTTTCTAAT | 5521 |
rs182127056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059332 | TTATAAAAAATGAAA[A/G]GAAACACCTCCTGTT | 5521 |
rs182130787 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823868 | TCAAGTTAATTTGAA[A/G]AAGAAAAGTTGGCTC | 5521 |
rs182134198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756182 | TTTGTAACATAAGCC[A/G]CTGTTCCATAGAGCT | 5521 |
rs182138439 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790208 | GTTTTCCTGAAGACT[C/G]TTCTCACTTGAGATA | 5521 |
rs182145672 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773719 | TTTCTGCATGTTTAA[A/T]TTAAGGCACAACTCA | 5521 |
rs182146458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731538 | CTTCCCGTAGAGTTT[A/G]ACTGACTAATTAAGA | 5521 |
rs182148593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739548 | GGAGTGCCAGGGCTG[C/G]GCAAAGGAAGGACAC | 5521 |
rs182151992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604201 | ACTGTGTTATCAGAC[A/G]GAAATCATGGTGCTA | 5521 |
rs182152412 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647551 | AAGGGTGAATGGCAC[A/G]GTCTCATTTGTATGC | 5521 |
rs182152996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757023 | TCTGAGTGAGAGTGG[G/T]GTTTTCTTGTTTTTA | 5521 |
rs182158425 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632428 | CATGGTACTTTGTTG[C/T]AGCAGCCCTGGTAAA | 5521 |
rs182167854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992603 | GGGGCACCTTATCAC[C/T]GCCAGGGTGTTGGGG | 5521 |
rs182170484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723317 | TTTGTGCTACATCCC[A/G]TCAGTCATTCAGCTT | 5521 |
rs182183486 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978154 | TTTTTTCATATGTTT[G/T]TTGGCCACTTAAATG | 5521 |
rs182195638 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695222 | ATCTTTTTGCTTTTT[A/G]CTTTAAAAGACTTAA | 5521 |
rs182197997 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005553 | ACTCCTTGCAAAAAC[C/T]CAAGGAGGTGGCAGT | 5521 |
rs182200826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042319 | CGTCTCTTGGCTGCC[A/G]GCTAAACAAGCGGAC | 5521 |
rs182202317 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023631 | CAGGGCCAAAATGGG[A/T]CAATTCATACTAACT | 5521 |
rs182207894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689162 | AAGGGAACTAACATC[A/G]TTGAGTGCTTTTTGT | 5521 |
rs182209359 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635712 | GTACTGAGTCCCAAC[A/C]CTTCACTCTCTGGGA | 5521 |
rs182210790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071284 | GGCTCCCTGCCTCAT[A/G]ACTTATTATGTGAAA | 5521 |
rs182213491 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659691 | TAGGTACTAAGATCA[C/T]TGTCATTTTATGGAT | 5521 |
rs182223209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598682 | CTTTCTTTTCCTGTT[A/G]TATCCCGCATCAAAT | 5521 |
rs182223586 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003901 | AACTCACTCGAGGGT[C/T]AATTGATTCTAAAAG | 5521 |
rs182225405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630685 | TCATGGAAGTTAGCT[A/G]TGAATACGGCTGTTG | 5521 |
rs182228885 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961439 | AAAGTGTCTATTTTG[A/C]TCTATCTGTAACAAC | 5521 |
rs182242586 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006606 | TTATCCTACTACCAC[A/T]CTCTCAGAGGATTTC | 5521 |
rs182256148 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980702 | GTGGTCTCTGTTATA[C/T]TGATTTACAGTATCT | 5521 |
rs182285317 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892555 | AACTTCTTAAGATCA[A/T]CAGGCCTTCAGTCTT | 5521 |
rs182296754 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912279 | TCCCTAAGAGAGGTA[C/T]AGCATACCCTAAAGA | 5521 |
rs182315144 | snp | A/C | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861609 | TCACCACAATGGCAG[A/C]CTTACTGTTTTTATT | 5521 |
rs182317222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146924025 | GAGCTAAATGATGAA[A/C]ACATATGGACACATA | 5521 |
rs182324233 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976870 | CAGCCACCCCATCAA[C/T]ACCTTCCTACCCATC | 5521 |
rs182325570 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949011 | ATGTATCTGTACTTG[C/T]AACAGAACTTCATGG | 5521 |
rs182337933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676182 | TGCCAGGAACTATCT[A/T]GGCGGCTTTTCCATG | 5521 |
rs182339531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692141 | CACCAGCACCCAGAA[C/T]AGTGCCTGGCACACA | 5521 |
rs182341607 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834308 | CAATGACATTCTGAT[A/G]GAATGGGTGACTTGA | 5521 |
rs182342701 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945874 | ACGTGTCAGATCTTT[C/G]TAATAGCCAGGTGTT | 5521 |
rs182344629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872342 | CTCGCATTTCAGGTT[C/T]CTCTGAGAACAGCAG | 5521 |
rs182352920 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657894 | TACATTTAGACTGAC[A/C]GTATATATCAAGGTC | 5521 |
rs182355152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804232 | AGCACTACTTCCTAT[A/G]CACTAGGCATTGTTA | 5521 |
rs182358716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644355 | CCCCTGAACCCACAT[G/T]GTTGAATTAGCTAGC | 5521 |
rs182361720 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628659 | AATGGAATTAAGATG[C/T]TACTGCAGAACCTAC | 5521 |
rs182363777 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807392 | GGAAAAGTTTGTCTT[C/G]GTTCTTCCCTATCTT | 5521 |
rs182365518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854379 | TCAAGTTATGGTATT[C/T]GGGTTATTTATCACC | 5521 |
rs182367026 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830415 | TGATAATGTATATAA[A/T]GCCCAACCAACAGTA | 5521 |
rs182368998 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888448 | TACCATGCTCCAACT[A/G]TCATCCTATCTCACC | 5521 |
rs182375291 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765628 | GCTTTGTTTCTTAAC[A/G]TCTACTACACTGGCT | 5521 |
rs182376215 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841105 | TGAGCCTAGACACTT[G/T]AAGCTTATGGAGGAT | 5521 |
rs182380433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822128 | TTTTCCTAAATATGC[C/T]TATTTTACAAGAAAA | 5521 |
rs182380606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858491 | GGGGCAACTGCAGTT[A/G]GAGGATTTAAGTAAT | 5521 |
rs182382241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754116 | CTGCCACAAGCCCCC[A/G]CCACGTGTCAGATGA | 5521 |
rs182399019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772617 | AGTGGAATGCATTCC[A/C]CTAATGCAACCAAAA | 5521 |
rs182401931 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736465 | GAGTAAACTGAGGCC[C/T]GGAGAGATAACTAAC | 5521 |
rs182402364 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770054 | GAGAATTTGGCTGGG[C/T]GTAGTGGCTCATGCC | 5521 |
rs182412935 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960785 | AGTAGTAACTTTTAA[A/T]ATCAAATAAAAAGAC | 5521 |
rs182417611 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946093 | TTCTATAAAATGATT[G/T]ATCTAAAATCTCTTT | 5521 |
rs182419080 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928810 | CCCATTTTGCTTAGG[A/G]AAAAAGCCAAAGGCT | 5521 |
rs182424309 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738474 | GTCATCTTATTTTAT[G/T]CATAATTTGGTACTA | 5521 |
rs182433344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977235 | CTTTAATAACCTCTT[C/T]TTCTTTTTTAGAATT | 5521 |
rs182434187 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705614 | AACTGTGGTCTCCTT[C/T]TTGGGTCCTGGATCA | 5521 |
rs182444121 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881066 | GAGCTGGGGGGCGGG[A/G]TGGGGGAGAGAGTGG | 5521 |
rs182451954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859590 | ACAATCCTACACATG[A/T]ACTTCTAAACCTAAA | 5521 |
rs182456416 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873246 | CTCTATTACGTATCT[G/T]AAATCCATCTAATTC | 5521 |
rs182465343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814056 | TAAAGCCATGACTTC[A/G]GACACATAGAACAGG | 5521 |
rs182465977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706545 | TCCTACTTGGTCTGC[C/T]GAAGGGCGGCCTCCA | 5521 |
rs182473489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912707 | AGAGACGGGGTTTCA[C/T]AATATTGGTCAGGCT | 5521 |
rs182477579 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897167 | GGTAAGTGGAGGAAT[G/T]ATGACAGATTGAGGG | 5521 |
rs182478719 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827945 | CCTTGAGAAAGAGAG[A/C]AATCTCTGCCTTGCT | 5521 |
rs182481470 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646730 | AATTAGCAGAATAAA[A/G]GCTACCATTCTAATG | 5521 |
rs182481906 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842943 | CCTGTAATCCCAGAA[C/T]TTTGGGAGGCCGAGG | 5521 |
rs182485039 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672606 | CAACACAGAAAACTG[C/T]TTGCAGAAACTGAGA | 5521 |
rs182494277 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641011 | TAGTTTGACTCAAAG[A/G]GGTTCCAGGGATAAA | 5521 |
rs182495189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052880 | TATGAAAAAGCAGGC[A/G]TGAGGGCTCAGAGTG | 5521 |
rs182496889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594503 | AGTGGCAATAATAAC[A/G]GGCATACCCAATATG | 5521 |
rs182498906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015602 | GGTTGGCTGACTCTC[A/G]TAACACAACACAGTA | 5521 |
rs182498944 | microsatellite | (T)10/11 | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727304 | GGATTATGAGAGGTG[(T)10/11]ACTTATTTAAAAATT | 5521 |
rs182499241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022845 | AAAACCCAGTCTAGA[C/T]AGAACCAGTGAAAAT | 5521 |
rs182500551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799078 | TCCGGGGCAGCCAGA[A/G]CAAAGCAATGGCCAA | 5521 |
rs182501281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609101 | GGAATTTATCCCAGG[A/G]ATGCAAGACAGTTCA | 5521 |
rs182506466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990471 | AGAATGCACACTGAG[A/G]AAAAACAGTCCCAAT | 5521 |
rs182526677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033834 | TTAATCCAAGCCTCT[A/G]TCCTTTCTTGTCCAC | 5521 |
rs182530124 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068608 | AAAAGACATCTTTGG[A/C]ATGCTGTAAGATACT | 5521 |
rs182538349 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052246 | ATGTAGGAGTGAATG[C/G]TTTTCAGAATATTTT | 5521 |
rs182554493 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928430 | CTTTTTCCATCTTGA[C/T]TGATATTAATTTATC | 5521 |
rs182558221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017629 | GAAAATAAATTTGTT[A/G]AAGCTAAGAGGGTAG | 5521 |
rs182571265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986219 | TATCAGTTTGGGAGA[C/G]AGAGAGAAAAGTGTG | 5521 |
rs182583008 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960109 | TTCAGGACTTAATGA[A/G]TAGAGGTCATCTACC | 5521 |
rs182583899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897663 | AAACAAATATAAAAA[C/T]ATATACTGGAGACAA | 5521 |
rs182608475 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607789 | GAAGCTGAGCCTTAA[A/C]TGATCAAGAAGCACT | 5521 |
rs182613635 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929498 | GAAATGTCAATAGAC[G/T]CCATGAAAAAGAAGA | 5521 |
rs182628548 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817762 | AACTTAGTGGTATGC[A/G]CCACTTTACATCTCT | 5521 |
rs182630747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870017 | CTCAGCAGCATCTTG[C/G]TACAATATTCCCTAT | 5521 |
rs182631855 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958363 | TTTGAAGGAAATATC[A/C]CTAGTAGATCTGCCT | 5521 |
rs182633780 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943208 | TCCAGAGATTCTGAT[C/T]GAACTGAGTTTTATT | 5521 |
rs182642031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866648 | TATATACACACACAT[A/G]TATATGCACACAGAG | 5521 |
rs182643075 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750204 | CATACTATAGCCATA[C/T]AATAAATCTTAAAAT | 5521 |
rs182647176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783841 | TTTTGCTACTGTCTG[A/T]TCGGGGGATAGGAAG | 5521 |
rs182657107 | snp | A/C | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972892 | TTATGAGAAATAAGC[A/C]TTTTCTCTGTAATGC | 5521 |
rs182666270 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753478 | ATTTTCACCAAAGAT[A/G]GACACAGTAAATAAG | 5521 |
rs182675840 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777950 | CTAATAAAAAATTGT[A/G]TGGTAGCCCAGCAGG | 5521 |
rs182680659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719557 | GAGCTTAGCATGATG[C/T]CTTGCACATTGTAGC | 5521 |
rs182683819 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812815 | TATATATATATATAT[A/G]TATATATATATATAC | 5521 |
rs182685855 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082642 | ATCATGGGGAGGGCA[G/T]TATTATCATCCCCAC | 5521 |
rs182688212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736063 | TGAATCATGGGAGCA[A/G]TTTCCCCCATCCTGT | 5521 |
rs182691795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700832 | GTGTAACATCCAGGC[A/G]TAGAAAGATAAGGCC | 5521 |
rs182692413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924885 | CATCCTTTTTTATGG[C/T]TGCATAGTATTCCAC | 5521 |
rs182696003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910116 | TCAGTTTTCATTCTC[C/T]GAATTCATTTCAGGC | 5521 |
rs182698411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723979 | TCCTGAGGACTGTAA[A/G]TTCCTTGAAGGCAGG | 5521 |
rs182699186 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719845 | TTTAAACAATTGAGA[C/T]TTTTCAGTTTCTTTA | 5521 |
rs182704817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687350 | GATCAAAGCTTGGTT[C/T]TCAGCCCTGCATGAT | 5521 |
rs182705045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893549 | CATAGGCCAGGTGCT[A/G]TGGCTCACACCTGTA | 5521 |
rs182709730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684202 | AGCCCCCAGAGCAGC[A/G]ATAAATCACAAAATG | 5521 |
rs182710355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877439 | CCAGAGCACTATTTC[C/T]CCAGCCACCTTTTTA | 5521 |
rs182714342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684868 | AGAGTCCAACTCAAA[C/T]CTTCTAAACCAGCAT | 5521 |
rs182716210 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666947 | GTTTTGAACTTGAAT[A/G]TGATTTCCTAACCTC | 5521 |
rs182718940 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742879 | GAAGGCGATGAAGGC[A/G]AAGGCAGAGATGGGG | 5521 |
rs182719650 | snp | A/G | 0.00133697 | 0.0258205 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650753 | GAAACAAATCACTTC[A/G]GAACCAAAGATCTTC | 5521 |
rs182722399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637104 | AATGCTTCCTGGGTG[C/T]ATCTTGCCTCATTAG | 5521 |
rs182733685 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034154 | TAAGCTCATTATTGC[G/T]TAAGGTCCCTTTTAC | 5521 |
rs182737771 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779443 | TGACATCCCACACTG[C/T]AGTTCATGATTGGTG | 5521 |
rs182740469 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806058 | GCAGATAACATTTTA[C/T]TCATCCTGAAAATAC | 5521 |
rs182742583 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049058 | GGGTGAGAGGAGAGG[C/T]AGAGAGAGAGAGAAA | 5521 |
rs182742747 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761631 | GTAATAATAAAATTT[A/T]AAAAAAAAAAAGAAA | 5521 |
rs182748736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654469 | TGCGGTTTAACCTAA[C/T]ACTTTGGAAAGGCTC | 5521 |
rs182750406 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798237 | ACTCGGTTGCCTCAT[G/T]TTGTTTTTCATCTTC | 5521 |
rs182756523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066109 | ATTATTGATTCCCTT[C/G]AATGTTTACTTTCTG | 5521 |
rs182757227 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744076 | ATTTAACTATACGTA[A/G]TATACATACTAACTT | 5521 |
rs182766300 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068969 | AACAATAGATGATAA[C/T]GACCCTTAAGAAACA | 5521 |
rs182766311 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624008 | GAGATCCCCCCTTCT[C/G]CATCTTACAGGGCCA | 5521 |
rs182771665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728310 | ACTGTGTGACTCCTA[C/T]AAACAGAATATTTTT | 5521 |
rs182778215 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692501 | GGAGCTGGAATGGCG[C/T]GCCCTACATGCAGGC | 5521 |
rs182783138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711250 | TTTTTTTTCTATGCT[C/T]ACAAGTCATCAAGCA | 5521 |
rs182783844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623527 | GTTTGATTTCAGTCT[G/T]TTTCCTAAGCTTGAT | 5521 |
rs182796974 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676489 | TTTGTGCATGTCACC[A/G]CCTCTGCCTAGAACA | 5521 |
rs182831958 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001074 | AAAGGTTTGTAAATT[A/C]TCCAATCAGCACTCT | 5521 |
rs182834452 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906138 | TGAGATATGTTGGAA[A/G]TGTAAAATACACAAT | 5521 |
rs182852957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913151 | TATATTCGGCGGAAA[C/T]AGTCTATTTCCTGTG | 5521 |
rs182853908 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969123 | ATAGTATGAACTGCT[C/T]TGTAAGAAGTAAGAT | 5521 |
rs182868186 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937295 | GACAGAGTGAGACTC[C/G/T]GTCTCAGAAAAAAAA | 5521 |
rs182868206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991119 | TTCTTGTACACTCTT[C/T]GTAGGAATGTAAATT | 5521 |
rs182882781 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881519 | CCAGGTTCAAGTGAG[C/T]CTCATGCGTCAGACT | 5521 |
rs182885994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946456 | TTTTCAAAAGGCAGT[A/G]CAATCAATAGTGTTA | 5521 |
rs182904689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893013 | TCACAAACCCTATGC[A/G]CAGAAACAGTGGGCC | 5521 |
rs182914687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852017 | TTGCTGAAGAAATGG[C/T]GATGCTTTGAGAAAA | 5521 |
rs182919914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851467 | TCCTGTTCCATGTGA[A/G]TGAGATCATGCCCAT | 5521 |
rs182926500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827052 | AAGTTTCTGCTTCTT[C/T]CCCATTCTTTTCCCC | 5521 |
rs182930598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847004 | CTATAATACATCAGA[C/T]TATGGGTGGGAAAAC | 5521 |
rs182936395 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862324 | TGTGTGCCAAGAACC[C/T]TACTGTCCTTTGTAT | 5521 |
rs182944746 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877026 | TTTCCACATACATTT[C/T]CTCGCATGGATATTA | 5521 |
rs182951358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816453 | TATATGACAATAGAA[A/G]TTTAGTAAATTTTGG | 5521 |
rs182954214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803635 | TAAATTTTTCAAAGC[C/T]CTATGACATGTGCAG | 5521 |
rs182958945 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829842 | AAATTTTGATAATCT[A/C]TTTTCATTGCAGGCA | 5521 |
rs182961813 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821615 | TCTCTTACTAGCTTG[A/G]GAAAGTAAATTCCCT | 5521 |
rs182968775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797498 | ATAACACCCATCTTT[C/T]TGGCCTCTGGAGGGA | 5521 |
rs182972382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650122 | GTGCTTGGAACTCAA[C/T]AAATGTCAGTCACTA | 5521 |
rs182975222 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636241 | GGGTACCTGTATATA[C/T]CCTTGGGCGTTAGGA | 5521 |
rs182983402 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619343 | ACATTAGCTGGGTGC[A/C]GTGGTGTGTGCCTGT | 5521 |
rs182988717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783132 | ACAAATTAAGATTAA[C/T]GTCATGGGCTTTATA | 5521 |
rs182989318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787060 | GGCCATGTGGATCTT[C/T]AGTAGCAGATGTGGG | 5521 |
rs182990791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728067 | ATGTATAATTTTAAA[C/T]ACCACAAAGTAACTC | 5521 |
rs182992204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761511 | ACACACTGGGGACTG[C/T]TGTGGGGTGTGGGAA | 5521 |
rs182993778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599086 | AGTTTATCTCCAGCA[C/T]TTGATCTTTGCTTTC | 5521 |
rs182996203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702166 | GAAACAGTGAGGTGG[A/G]AAACTAAGGCAATTA | 5521 |
rs183001043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019629 | ATCTATTACTTTGAA[A/G]GAGGATATGTTAAAA | 5521 |
rs183001629 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075719 | AAAACTATCTTAATT[A/C/T]CTTAGTTTACTTCTC | 5521 |
rs183002717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982196 | TCTTCTTTCTAATCT[A/G]TACATTTAGTGCTAT | 5521 |
rs183014034 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964989 | ATTTGTCTCTAACTT[C/T]CCTTCCAATTCTAGC | 5521 |
rs183016326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951388 | AGTGTATATGTGCAG[C/G]ATGTGCAGGTTTGTT | 5521 |
rs183019599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008756 | TGAGGGTTTCTATTC[A/C]CACACATCATCTTTG | 5521 |
rs183025615 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037730 | TGGGAGCAGCATTTC[C/T]TAACTGCCCACTCAC | 5521 |
rs183033255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997130 | GTTAAACATTCAGAG[C/T]ATCCCCATCTTCTCA | 5521 |
rs183045078 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691227 | GCTGACTTTCCACAG[C/T]TTCACAGTTTTATCT | 5521 |
rs183046902 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589551 | TTGATTTTTTTCAAT[C/T]AAATGGAATTGCTTA | 5521 |
rs183055461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038340 | GAGAACGAGTTTGAT[A/G]GAGGAATACTATATA | 5521 |
rs183058710 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933654 | CCTATCGTGACAAAC[A/G]GAAGTTCTTTTTTTT | 5521 |
rs183065970 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640325 | GGGGCATGTGAGTCT[C/T]CTGGATTCACAAAAT | 5521 |
rs183066193 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988997 | AAATAAATTGGTAAA[C/T]CTAGAAGAGAGTAAT | 5521 |
rs183068116 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608172 | AGACAGGGGAATCAG[C/T]ATGAATAAATGCCTG | 5521 |
rs183068832 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918629 | CTCTCTCTCAACCTC[A/T]TCTAATACCACTCTG | 5521 |
rs183071545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002831 | CATTGCAGGTTTTTG[C/T]GCAGGGGGAGAAACA | 5521 |
rs183074543 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973544 | TGGGTTAGTGGCATT[A/T]CTTTAAATCTACAGT | 5521 |
rs183077123 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599805 | CCTCCCTGAGCCCCC[C/G/T]ACCCTCTGACAGGCC | 5521 |
rs183080808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985750 | AGAGAAACAAGAAAA[A/G]GCATTTAAATAGAAA | 5521 |
rs183083139 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603540 | TATTTGTGGAGTGCC[A/G]GCTTTAGGTAGCACA | 5521 |
rs183085607 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628058 | CAAGTGATTCTCCTG[C/G]CTCAGCCTCCTGAGT | 5521 |
rs183089479 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064542 | AATGGACACATTAAT[A/T]GCATATTAGGCAGCA | 5521 |
rs183094571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073479 | GCAAAGTGAAGTTGC[A/G]TAGGAAATCCCCCTG | 5521 |
rs183095698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055911 | ATGGGTCCCATTTTG[C/T]CATCAGCGCCAGGAA | 5521 |
rs183099579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020273 | CAGAGTTCCTTGTAC[C/T]ATTTATTTAAAGCCC | 5521 |
rs183099822 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039669 | CTTCTGCAGTTAAGT[A/G]TATGCAAGTTCATCA | 5521 |
rs183100889 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081958 | TTTACATATTCAAAA[A/G]AGTCCTTTACAGAAC | 5521 |
rs183127982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922691 | CCATATAGCCCATGT[C/G]CTTGGAGGAAGTACA | 5521 |
rs183130988 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002735 | ACCAGGGTCCAGGGA[C/T]CATTGCGGGTTCTCG | 5521 |
rs183141842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958865 | TCACAACAAACTTAT[A/G]CAATAGGTTCTATTA | 5521 |
rs183146350 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889642 | TTGCCTTATGCATCT[A/C]TTTCTTTGGTTTATT | 5521 |
rs183162687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954998 | GATGAATAACTTATC[G/T]GCTCGATGGTCCTCC | 5521 |
rs183171284 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723907 | CAAATCTCATTAATC[C/T]CTTTTTTCTCTGAAC | 5521 |
rs183176936 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739089 | TAGTGGTGTGATCAC[A/G]GCTCACAGCAGCCTT | 5521 |
rs183185195 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705803 | ACTCCTACTGGGATT[A/T]TGCCAAGATGACCTT | 5521 |
rs183188179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648473 | TGTCTACTGGATAGC[A/G]CTACTTTGATGACCT | 5521 |
rs183192468 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687027 | TAAGTGTGTGTGTAT[A/G]TGTGTGTGTGTGTGG | 5521 |
rs183194755 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633499 | CTGGGGCTCGTAGCC[A/G/T]CAGCAGCTGAACAAA | 5521 |
rs183204306 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617056 | TGAAAAAGAATGAGA[A/T]CCTGTCACTTGCAAC | 5521 |
rs183206485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653577 | CTGCAGGACTTCCTG[G/T]GGCTCCTCCTAAACT | 5521 |
rs183211866 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884336 | GAGGGTTTCCCATAT[A/C]CATCAGAGGAAAATT | 5521 |
rs183214092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950754 | TCTTGCTTGAATAAA[C/T]GTCAAAAGAGGGTGA | 5521 |
rs183215764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863219 | GTCTTGACTTCTAAA[A/C]CATAGTATGTCAGTT | 5521 |
rs183215922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866145 | GCTAAAATACTTATC[A/G]TCTGACCCTCTACAG | 5521 |
rs183217006 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782000 | ATTTCCCTTGGTACT[A/G]TTGTCACGATAATAA | 5521 |
rs183224412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917688 | TTAATATTCTAATAC[C/T]ACAGTGGCTGGCAAA | 5521 |
rs183225327 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764351 | TTGGATATATCACTT[C/T]GGCTTTAGGGTGGAA | 5521 |
rs183225909 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806882 | GCCCCCGACAGGGGA[A/G]CAGGCAATAGGGGAC | 5521 |
rs183228376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802659 | TTATTTAGCCAGATA[A/G]GACATGGGATTTCCT | 5521 |
rs183235781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827378 | ACCATAGATCAAGGC[A/G]TAGAGTAAGGTAAAA | 5521 |
rs183246356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713711 | ATTTGCTGATGGATT[G/T]ATTATAGGGTTTGAA | 5521 |
rs183250182 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833473 | TACTAAATTCCCCCA[G/T]CCTATTTCAACACTG | 5521 |
rs183262199 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933201 | AATCCCATGTGTTTC[A/C]AACCAGATGAATTTT | 5521 |
rs183262436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748418 | TCTGACATTGATACA[A/G]TGGAGATACAGACAA | 5521 |
rs183264402 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732389 | AATACACAGAAACTA[C/T]GGTTTTTCCACAGAG | 5521 |
rs183268398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696077 | TTTTTTCCCATCCCC[C/T]CGCCAACAAAGTAGT | 5521 |
rs183270581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917910 | CAATCTGACATCTCC[A/T]CCTGATTAAAACAGA | 5521 |
rs183271255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673370 | GTTAATAATGAACTT[A/G]TGCTGGAAGAAAAGA | 5521 |
rs183274342 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655273 | GCCCCAAAAGAGCAG[C/G]CTGAATCTAATCTGC | 5521 |
rs183275582 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769903 | CATGTACTTGTCTTT[A/G]ACCTAGTTATTCTAG | 5521 |
rs183277535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641798 | AGAAGATGAGCAATT[C/T]GTGGCTCCACGTATA | 5521 |
rs183290899 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768796 | TGGAGATTTGCTGTC[A/G]CATCTGCCTAGTGTT | 5521 |
rs183295892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870323 | TTAAGGAGATAATTA[A/G]GATTAAATGAGGTCA | 5521 |
rs183301736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885315 | CATGCTCTTAACCAC[C/T]GTGATTTGAGCTATT | 5521 |
rs183304615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593380 | ATCACCATTCATGCA[A/G]TCTTTTATTCAACAA | 5521 |
rs183310989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824193 | GAGCAGAAAGCTTAT[C/T]GAACATGAGGCTATT | 5521 |
rs183311397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900990 | TGGCTGCATAGTATT[C/G]CATGGTATATATGTA | 5521 |
rs183314384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838387 | GACCAGCCTGGCCAA[C/T]ATGGTGGATCCCTGT | 5521 |
rs183314556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735808 | GATCCTACCTGATGA[C/T]ACTGGAATTTCAGGA | 5521 |
rs183322109 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675978 | AATAGGGAGCTGTCA[G/T]GTTCTATGACCCTCC | 5521 |
rs183322186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700445 | GAAATGGGTTTATGA[G/T]AGTTACTGGAAGTTA | 5521 |
rs183322914 | snp | C/G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854627 | AAAGTAACTAAACTT[C/G/T]TGAAAATGACACCTT | 5521 |
rs183332142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644995 | TAGGACGCTTTTCTG[C/T]AGGGCTGAGTATTAT | 5521 |
rs183332161 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048299 | TCAGGCAGTATGGGT[A/G]CATACCCTGATCTAT | 5521 |
rs183333634 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019884 | CTATGGGAATACACC[A/G]CTCAGATCTCGTTTC | 5521 |
rs183335481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620213 | TAAAGAAAGGGGAAG[C/T]GAAAACCTGTGTTTG | 5521 |
rs183335581 | snp | A/G | 3.59176e-05 | 0.00423763 | intron-variant, missense, synonymous-codon | PPP2R2B | GRCh38.p7 | 5:147055735 | CAGGTAACGAGAGAA[A/G]CATTTCATCTTCCAA | 5521 |
rs183340593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666089 | TAGAAACAATGTGAA[C/T]ATCTATCAATGGAGA | 5521 |
rs183341003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594291 | AGAAACAGTGTCAGA[C/T]TTCTGGAAGGCACCA | 5521 |
rs183343721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644167 | TTAAAAATAATATCA[A/G]TAAAAGAATATCGTA | 5521 |
rs183344713 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082210 | GCCATAGATTTTTAT[C/T]GAATTCCTATACGGA | 5521 |
rs183350206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059756 | TGTGCTCTGAACTAG[A/G]CTGCTCTAAGCTTTT | 5521 |
rs183356552 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608663 | AGCTGGGCATAGTGG[C/T]GCATGCCTATAGTCC | 5521 |
rs183365459 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079905 | CATCTTGGTTTGATA[C/T]CATTACACAATATAC | 5521 |
rs183399343 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987962 | AACCAAAGAGGGCAG[A/G]AGTAGCTATACTTAT | 5521 |
rs183415205 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988500 | ATAGAAATTAAACAA[C/G/T]TTGCTCATGAAAAAC | 5521 |
rs183427013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900247 | CAAAAATAAGTGCCA[C/G]AGTCAGAAAACATAC | 5521 |
rs183432545 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924246 | TAAAGAAAATATCAG[A/C]TACTTAGATAATGAT | 5521 |
rs183441772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847222 | CATGCTGCCTTCTTG[C/T]TTGACCTGCCTGTAG | 5521 |
rs183455748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775204 | CAAAGAAAACTATAA[A/G]CTAACACATTTTATG | 5521 |
rs183458333 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932427 | TACCCCTATACTGCT[C/G]TTCTTGTGATAGTGA | 5521 |
rs183462969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957703 | CTCACCATAGTCATC[A/G]TAGTTTTGTACATTT | 5521 |
rs183464544 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759390 | AATTAAGCCAACCTC[A/G]TAACACTCAGGGAAA | 5521 |
rs183466808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795257 | ATATTAATTGCAGCA[C/T]TATTCACAATAGATA | 5521 |
rs183467961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870602 | TTTTAAAAATGCAGT[C/T]TGAGCTGACTAATAC | 5521 |
rs183471957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813094 | CAGGACATATATATA[C/T]CTACATATACATATA | 5521 |
rs183483740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901260 | ATCCCAGCACTTTGG[C/G]AGGCTGATGTGGGAG | 5521 |
rs183484703 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841925 | ATCCCAGAATTTAAA[G/T]TATAATGAAAATATA | 5521 |
rs183496389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968528 | CAAGATTGAAACTAC[A/G]AAGATCTATGTCAGT | 5521 |
rs183498941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985212 | TTTTAGTAGAGACAG[G/T]GTTTCACCATATGGG | 5521 |
rs183499510 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838903 | AGCGTTAGAGGTTTA[A/G]CCCAGTCTTCCTCAC | 5521 |
rs183507992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913595 | CAGCTCACTCGGTCT[C/T]TTGATCTCCACTTTG | 5521 |
rs183511045 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954689 | AATGAAAAGAGAGCC[A/G]AGATCTTTAGAGAAA | 5521 |
rs183514031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014919 | AATAAAAAAAAATGA[A/G]TTTCATAGACTGGGT | 5521 |
rs183522997 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033019 | GTTCACTGCATCCAC[A/G]CCAACATCTACTGTT | 5521 |
rs183527950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999786 | CCCCAAACTCACAGA[C/T]AAATCCTCAGATGTG | 5521 |
rs183537133 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752715 | ATGGATTAAATAGTA[C/T]TGATTATCTGTGGCA | 5521 |
rs183540207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786209 | AGGAAAAAAAGAATC[A/G]CTCAAGATATGTAGA | 5521 |
rs183550631 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936493 | AAAAAAAACCCTAGA[C/G]AGTTATGAAGGATGG | 5521 |
rs183552496 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897915 | GTAGGAAAGGCCAGG[C/T]GCAGTGGCTCACGCC | 5521 |
rs183555721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922365 | CTCTCCAGGACTCTC[C/T]CTCCTAGCTCAGAGA | 5521 |
rs183562749 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719075 | AGCACCTTCTATGTG[C/T]CTGACCTAGGACTTT | 5521 |
rs183570648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683767 | TTAAATTCTCGTGGA[A/G]GGCTTTCTGATCCCA | 5521 |
rs183572094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658157 | GACAAAGATGAGAGC[A/G]GAAGTCCTGGGTGTC | 5521 |
rs183577828 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749436 | TTTAGCATAAGAACT[C/T]TTTGCCTAGCCTAGA | 5521 |
rs183585404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714879 | CTTTTCTGCTTTCCA[C/T]TCATCTCTTCCTCCC | 5521 |
rs183586153 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628809 | CCATAAGCCCACATC[A/C]CATGATCACTTCACC | 5521 |
rs183587666 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064899 | TACCAGTTTGGGCAG[C/T]AGAATGAATTTTCTT | 5521 |
rs183591033 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955119 | AAACCATAATTTAAA[C/T]ATAAGCAGTCTTTAC | 5521 |
rs183591805 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681486 | AGAAATGGGACCTGG[C/T]GTGGGCTGAATGTCT | 5521 |
rs183601262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938832 | GATGGAGTGCATGGA[A/G]TGCAGTGGTGTGATC | 5521 |
rs183613503 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002695 | TGTTTCTGCTGCTGC[A/G]TCGGTGGGCGCAACT | 5521 |
rs183627247 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853576 | TACCTCAAAAGGTGA[A/T]TTCAAAACCCTAATT | 5521 |
rs183639787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922957 | GTGGAAATAATTTTG[A/G]AAGTGTAATGGAATT | 5521 |
rs183645788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823073 | TGTGAACCAAAAGGT[C/T]ACACATGCTTCTTCT | 5521 |
rs183645941 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808699 | CCTCATTTCTATCAG[A/G]GGAAAGAAAGTCCAA | 5521 |
rs183646070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906570 | CAGGTGATCCGCCTG[C/T]CTCGGCCTCCCAAAG | 5521 |
rs183652509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859690 | TGGTATGAAATAGCC[C/T]GAGAAACCTTTCTGT | 5521 |
rs183655298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029298 | TACACATTTTAAACA[C/T]TTCATCTGAAATTGC | 5521 |
rs183655816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889860 | AGGCAATGCTAATCA[A/T]ACATCTGGCAAAGTT | 5521 |
rs183656933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874271 | TTGGAACATCCCGTA[A/T]CACCTCTGCAAAACG | 5521 |
rs183658403 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733593 | AATTCCCATATTAAA[G/T]TTGTTCTAAGCTTGG | 5521 |
rs183658545 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836179 | CCTCCCCATGCAGCT[G/T]CCAACAAATTTATTA | 5521 |
rs183660844 | snp | C/T | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081062 | GATTTCTCCTACCTT[C/T]TGTGGTTCCAATCTC | 5521 |
rs183663457 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146772022 | TTTTCATGGGTGTTC[A/G]TTGCAGCATTGCTTA | 5521 |
rs183665100 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029759 | GCATAAAGGAAAGGC[C/T]ATGTGAGGTCAGAGC | 5521 |
rs183670202 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697218 | CGAATCCTCTTAATT[G/T]TTATGCTATTCAATT | 5521 |
rs183673100 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716378 | TCATTAAAGGCAGAA[A/T]TCCTATTTTACTCAA | 5521 |
rs183679622 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789303 | ATGTTGGGTATGTGA[A/C]ATAACCCTTTCAGTC | 5521 |
rs183683096 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681794 | TCTGAAATTCAGACC[A/T]TTTAACAACCAAGGT | 5521 |
rs183686239 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662957 | TCATTAGTAAAGAGA[C/T]GTAAATTAAGATTTT | 5521 |
rs183687786 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625383 | CAACTACTCTTTACT[G/T]TTGGCTTTTACATAT | 5521 |
rs183690741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649076 | GGAGACCAGATGAGA[A/T]TATTGCAGTCACAGT | 5521 |
rs183692081 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606813 | CTCATTTCAATGTCA[A/C]CCCCACCCTGGCTGT | 5521 |
rs183694101 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006511 | TCCATCAATGCAGGG[A/G]CATACAACGAATACA | 5521 |
rs183695680 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909606 | TGGAAGGCATTCACT[A/G]TCTTAAACTGGAATC | 5521 |
rs183698635 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634532 | TAGAGACGGGGTTTC[A/G]CCATGTTGCCCAGGC | 5521 |
rs183704315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855183 | GAAGGAAAAAAAATC[A/G]TACATTGAAATTACA | 5521 |
rs183704618 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025435 | CAAGCATTACCCCAA[C/T]GCTAAAGTCACGCGA | 5521 |
rs183710373 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972447 | CTGGGCACGGTGGCT[A/C]ATGCCTGTAATCTCA | 5521 |
rs183712742 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994274 | GGTGAAGGCTCAGAG[A/G]GGTAATAACTTGCGT | 5521 |
rs183717769 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885864 | GCTAAATGAAAGACA[C/T]CAGACACAAAAGATG | 5521 |
rs183719663 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044498 | TGCATAATATATTTT[A/C]TTTCTTTCTTTTTTG | 5521 |
rs183723068 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942556 | GAAATACAATGTCTG[C/T]GTAGAAGAAAAATAT | 5521 |
rs183726111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944051 | TTTAGCTACAGAGAC[C/T]AGCCTCCTCATCCTT | 5521 |
rs183729195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590534 | TTGGCTCAGAAAAGG[C/T]GTCCACTGGTTTTAA | 5521 |
rs183730835 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060522 | AGTCCCTGCCACTTG[G/T]GGGGCTGAAGCAGGA | 5521 |
rs183733455 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996745 | GAAACAAGTGAAAGG[A/C]AATCCTGAGGTTTCC | 5521 |
rs183758105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964472 | AGGACCAGCCCGCAA[C/G]AGCCCACTCTAGAAA | 5521 |
rs183771059 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765203 | AATAACTATATTTCA[C/T]ATTCATACATTATAA | 5521 |
rs183793608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732721 | AATCAATAGAAGAGG[A/C]ATACTACTAAGTAAC | 5521 |
rs183816714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696601 | AAAATTAAAAGGAAA[G/T]AAATTGAAACAAATT | 5521 |
rs183819912 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794229 | TTATGAAGGTCTTCA[C/G]TCTTCTTTTGTCAAT | 5521 |
rs183825272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816057 | TTATGAAACCTCCAC[C/T]ATCTTGACCACTCCA | 5521 |
rs183831264 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662480 | TGTTAAAAACTGATG[C/T]CTGCCTCCCCGGGGT | 5521 |
rs183841529 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846372 | CGACAGAGTGAGACT[C/T]CATTTCAAAAAATAA | 5521 |
rs183872177 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757906 | AGCTTTGAGGCCAAG[C/T]GGAACTCTTCCATGC | 5521 |
rs183880480 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007899 | CTCACTGTGAGGGTC[C/T]GCGGCTTCATTCTTG | 5521 |
rs183889919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730072 | GCCAGGAGGGAGGCT[A/G]TACCCTGCAAAGCCA | 5521 |
rs183894818 | snp | A/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047849 | CTTTTCTGCCAGATA[A/G/T]CAGAAGCCTTCACCA | 5521 |
rs183897132 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693618 | TAAGCAAAAAATAAT[G/T]TAGTATGAGTATATC | 5521 |
rs183898851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712152 | GGTATTATTATGTTA[C/T]GATGGTTTTTCAAGG | 5521 |
rs183908941 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950896 | TAAGAAATATTTAAT[G/T]CTTAGTGCCAAAAAT | 5521 |
rs183916197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771368 | ACAATAAATCCCTTG[C/T]GAACAGGTGCTACTA | 5521 |
rs183920823 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659396 | TTGAATGGTATAAGA[A/G]GGTTTTTAGAGTTAT | 5521 |
rs183929268 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662361 | GCAGTAGTAATTACT[A/G]GCAACACTTTGATTT | 5521 |
rs183934204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981792 | AATCTGTTCTCCAAT[A/C]CTATAATTTTGTCTT | 5521 |
rs183936088 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022075 | CAAACACAAAATAAG[C/G/T]TAAAAAAACAATAAA | 5521 |
rs183941581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630396 | CTCCCCACAAGAAAG[G/T]ATGGTCCTTAAAGGC | 5521 |
rs183946927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608909 | AAAAAATAGAGGAGG[A/G]AATACTTCCAAACTC | 5521 |
rs183949371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042877 | GAGGGAAGAGCATTC[C/T]AGACGGAGGGAGCCA | 5521 |
rs183949610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005925 | CTTCTCTGTAACCCT[A/G]TAACACTTCAATACC | 5521 |
rs183950896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633254 | AACACGGTTCTCCTC[A/G]GCATTTTGATTAAAT | 5521 |
rs183956162 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082893 | ATCAAGTAGTAAAGT[A/G]TCAATGTCTCCTTTG | 5521 |
rs183957483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755044 | TGACAACAATACACC[A/G]TTTATATAAACATAA | 5521 |
rs183957741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721808 | ACGCATACCTCTTAA[A/G]TAGCTCTTGCAACAA | 5521 |
rs183958083 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068229 | GTGTCGATTATTTTA[C/T]TTCATCCTCCTGACA | 5521 |
rs183958555 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041794 | ATAGCTTCATGGTGT[C/T]TAACACCTCAGTGAC | 5521 |
rs183966367 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077318 | CACACACACCCACAC[A/C]CACACCCCTAGCCCT | 5521 |
rs183966722 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779625 | CAACAGTCTATTACA[A/G]CTATGTTCCTTGCTG | 5521 |
rs183969220 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737992 | CCTACTCAGACCTGG[G/T]GACTATGTTCGACCT | 5521 |
rs183970562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057192 | CCACCAGTATGCCAC[C/T]TCTCTGGCCCTTGGA | 5521 |
rs183974834 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979359 | CATTTTATAAAATTT[A/C]ACACAATTTTCTTGT | 5521 |
rs183976842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704011 | CTATTGTCTACTTCC[C/T]TTCAGAGAATAAGCC | 5521 |
rs183983521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669609 | CTTGCTTTATGGGGC[A/G]ACTTTGGAACCTAAC | 5521 |
rs183983818 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685779 | ACAGGAGGACAGAAA[C/G]AGCCATTGTGTAAAA | 5521 |
rs183989491 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947811 | TTAGCCATGCAACCC[A/T]GTGTTCTCATGAGTC | 5521 |
rs183991038 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962518 | AAAAAGTAGCTGGGC[A/G]TGGTGGCACACACCT | 5521 |
rs183994609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652998 | AAAAAAGTGACTTTG[C/T]CCTGAGAAACACTAC | 5521 |
rs183997284 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946793 | CGAAGCCATTACAGA[A/G]GGATTGTTTCCATCT | 5521 |
rs184007984 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993367 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5521 |
rs184014148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006360 | CTTATTAATAGCAAA[C/G]AATAATTGGAATCCC | 5521 |
rs184014533 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898041 | AGTACAAAAATTAGC[C/T]GGGTGTGGTGGCAGG | 5521 |
rs184015049 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773969 | TGCAACCCGTCGTAA[C/T]AGGTAATGTCAGCCA | 5521 |
rs184017685 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810377 | AAACCATCAGATTGC[A/G]TGAGACTTACTCACT | 5521 |
rs184021163 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874898 | CAAGGCCCTTCCTCT[A/G]TATAACCCCATACAC | 5521 |
rs184021794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829495 | GTTCTTCTGAAGCCA[A/G]GCACAGCTAAAGGCA | 5521 |
rs184049452 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740436 | ATGGGAAGAGGCTGT[A/T]GTAAATGAAGGGCTC | 5521 |
rs184050005 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891065 | CCAGCAAATTTTTTC[A/G]TAGAGAATAAAAGTG | 5521 |
rs184050231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930357 | TGTGGCTGGTCATGT[A/G]GAGTGCTGGAGAAAA | 5521 |
rs184053088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889477 | AAAAACTCTAAATAC[A/G]AGGTTCAGATAAGTT | 5521 |
rs184053543 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706790 | ATGCTCTCGGCCTCA[G/T]CCCGACTGCGGTTGG | 5521 |
rs184057963 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914781 | ATAATGTAGACAGCA[C/G]ATTTGGTAGCCCAAA | 5521 |
rs184075167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859093 | TCATAGAAAGAGCTC[A/G]GTTTTATGAATCAGT | 5521 |
rs184097727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680885 | CCAGAGAATAAAATA[C/T]ATTTTTCTGTTGAAA | 5521 |
rs184101734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024287 | TTAATATATTAAATG[A/C]AGATTGGCCCTATAA | 5521 |
rs184103189 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051934 | CACCCAGCTTGAATG[G/T]CTTCTTTACAGCTAT | 5521 |
rs184110015 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648047 | CATGGTGGAGACTAG[A/C]TAGCTGTGTACCAAA | 5521 |
rs184121488 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616726 | TAAAAGGCAATAATG[C/G]TGATGAGGATGTGGA | 5521 |
rs184125434 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855605 | CCTTTTTCCCTCTTC[A/G]TTCCTTTTATTAAAG | 5521 |
rs184131575 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871294 | TCCGTCATATTTCTC[C/T]TGCTGTGGCCCAGGC | 5521 |
rs184136396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741442 | AGTGCTGCATATTCA[C/T]AAAAATCCCGCCTTT | 5521 |
rs184144219 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707827 | CATACCCACACACTC[G/T]CTCTCTATAGACAAA | 5521 |
rs184149752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811094 | CTGCAACCTCCGCCT[A/C]CCGGGTTCAAGTAAT | 5521 |
rs184155966 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825415 | TTGATTTGTTTAGGC[G/T]ACCTCAATAAAGTAT | 5521 |
rs184166194 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930122 | AAGAAAATAAATCAG[A/G]GTTATGTGATAGAAA | 5521 |
rs184167011 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839420 | AGCTACTCGGGAGGC[C/T]GGGGCAGGAGAATCG | 5521 |
rs184174464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674758 | TCAAAAGTTCTGGGA[A/G]CTTAGTTTACATCTA | 5521 |
rs184184733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993070 | GCCTCAGTCTCCTGA[A/G]TAGCTGGGACCACAT | 5521 |
rs184186674 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961686 | TGAAAACCCATTTTT[A/G]TAGCCTGAAATTTGG | 5521 |
rs184195856 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643183 | TATTACACACACACA[C/T]GAGAGAGAGAGAGAG | 5521 |
rs184211557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629327 | AACTCAAGCACCAAA[C/T]CTACGAGTTATCTTA | 5521 |
rs184218248 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608699 | ACCTGGGAGAAGAAT[C/T]GCTTGAACCCAGGAG | 5521 |
rs184226718 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976207 | AAGTGGTGCAATCTC[A/G]GCTCACTGCAACTTC | 5521 |
rs184226954 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009211 | TCTGTTCTGTTTTCC[C/T]CTTTACCCTGGCTTG | 5521 |
rs184231211 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668740 | CCAGCACTATGCTCT[A/G]TCCTTTTAGAACTCT | 5521 |
rs184231262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989598 | TAAAGGAACATACCT[C/T]GATACAATAAAGGCC | 5521 |
rs184233521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617726 | TTGAAGCAGAGTCTC[A/G]CTCTGTCACCGAGGC | 5521 |
rs184234645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651936 | CTCACCTATGCGGGA[A/G]TTTTTAAATCAAATC | 5521 |
rs184236275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872996 | CAAATTTATTATCTA[A/G]TCCAGGTCTTTCTCT | 5521 |
rs184238371 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997463 | GCACCCATGGACATG[A/G]CCTTTCAGCTGTGCC | 5521 |
rs184243728 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906048 | TTTGGACATTTGAAC[C/T]TATTTTTTCAGCTGT | 5521 |
rs184246323 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959629 | GAATGAGACAGAGAG[A/G]ACAATGGAAAGGTTT | 5521 |
rs184247419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638115 | TGAAATATAAAATAC[A/G]GAGCTGACTCCCACT | 5521 |
rs184253292 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997926 | TTCTCTTTTTGAAAG[A/C]AATGCAAAGTTTGAT | 5521 |
rs184254789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621551 | GGCAAGGATTAAACC[A/G]CTGGTTTGGGCTTCA | 5521 |
rs184256889 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030595 | GTATTTTTAACTTCT[G/T]AAATTTCCCTCTATT | 5521 |
rs184263934 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040985 | CCCCTCTTCACAGAG[A/T]TACTACTCAGGTCAG | 5521 |
rs184267098 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967161 | AACATACTGCCCTCT[A/G]TTAGATACATGGATA | 5521 |
rs184268550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983472 | GGCGTGAGCCACTGC[A/G]CCCGGCCCAGAGCGT | 5521 |
rs184269641 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895334 | ATAGCACCAAGTGTC[G/T]CCTTCATTACTTTCA | 5521 |
rs184272091 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031445 | ATTTTGGTTTTCTTT[G/T]TAGCAGTTCTACTAT | 5521 |
rs184276556 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056214 | AGCATAGTGTTCTGC[C/T]CTGGAGAGAGATGGC | 5521 |
rs184282076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010611 | TTGCTGATCTGAAAG[A/G]AGGTGGAGCTCAGGC | 5521 |
rs184287758 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945372 | GATAATTATTAACCA[A/G]ATGGATTTTATTTTA | 5521 |
rs184288999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076352 | GTAAACTAACCAATT[A/C]CTTGCACAGTATTTG | 5521 |
rs184290732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927852 | GATTCTCCTGCCTAC[A/T]CTCTCCTGTTCCCTG | 5521 |
rs184296584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930881 | CTAGTCTCTTGGAAA[A/T]AGCTAAACATCCAGG | 5521 |
rs184297996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688719 | CTTCTTTGCTCTTTA[C/T]CATAGGGATGGAATT | 5521 |
rs184301238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911843 | GTTGGGTATATACAA[C/T]GAATAAAGGTACACT | 5521 |
rs184320298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953094 | ATACTCAGTTACATG[C/T]CCTCCTGCTAATCAA | 5521 |
rs184321211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656410 | TAAGTAAGAAATGGG[A/G]TCTTGCTATGTTGCC | 5521 |
rs184321779 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898410 | TGGTGCTGGGAAAAC[G/T]GGCTAGTCACATGTA | 5521 |
rs184324370 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934508 | TCTGTTCATGTCCTT[C/T]GCCCACTTTTTGATG | 5521 |
rs184326389 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070505 | AGGCAGTAAGTAGGA[A/T]GATGCTGAGCCTGCT | 5521 |
rs184327214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962698 | TGGAGCCAATACCAA[C/T]TGATGACCCAATCAG | 5521 |
rs184352446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746577 | ACAGGGCTTCCAGGA[C/T]GACTCTGTCTGCTCC | 5521 |
rs184359843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868541 | TCCCCCATCTTCAAC[C/T]TCATTATAGTAGCTT | 5521 |
rs184360053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780874 | CTCATTTGTATATAT[C/G]TCACACCTCTTTCTA | 5521 |
rs184367243 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763196 | AGTGCTTTTGCTCCA[C/T]GACCTGCTCAGGGTC | 5521 |
rs184370242 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712466 | CAGGATAAAGGCAGT[A/G]TAGTAAATACTTACT | 5521 |
rs184374174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843374 | TTGCTTTACCAATAA[C/T]GTATAATATAAAACA | 5521 |
rs184376951 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730864 | TTATATCATTAAAAA[A/G]AGAGGTGATCAGGGA | 5521 |
rs184394035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595781 | AGAGCTTGGAGCAAG[A/T]GAGAACTTAAAACTC | 5521 |
rs184402131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814665 | GTAAGGGGAAAAGCA[A/C]CTCAAGTGAGCATGT | 5521 |
rs184404231 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774495 | TAACATTATTACTGA[A/G]TTTACAGAAAAAAAA | 5521 |
rs184422774 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740735 | TTTCACAATGAGCAT[A/T]TTTTTTCACAGATGA | 5521 |
rs184428982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969356 | CACAGTATTTCATTA[C/T]GGCTGGAATAAAGTG | 5521 |
rs184431739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915075 | GTTTTATGTACTACA[C/T]TGCTCTCAGATATAT | 5521 |
rs184434871 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744742 | TTACTGCAAGAAATT[A/G]TTTGTGGATCTTATT | 5521 |
rs184438578 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780145 | CTATTATGTGGCCAA[C/T]ACTTTGTAGAGCTGT | 5521 |
rs184438926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758249 | TGCCCCAAAGGCTCA[A/G]TCTGTAGCAGCAAAA | 5521 |
rs184439211 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725527 | TTAATTCTTCTATAA[A/G]TTGAAGGTGTTATAA | 5521 |
rs184447229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664358 | ATTCTAAATCCTTTG[C/T]TGTCATTTCAACAAG | 5521 |
rs184449419 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688364 | CCTTAGGGATGATAG[A/G]GTCCAGTGACCGCAG | 5521 |
rs184453995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980428 | TCCCTCCCCTCCCTG[C/G]TAGTCTCATCCAGAA | 5521 |
rs184458620 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707248 | TGCAGGAGGCTCCAC[C/T]TGGTCTCCAGCATCT | 5521 |
rs184460064 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674582 | TCCTAAGGAATGTAA[C/T]TGACAGCTCATACAT | 5521 |
rs184460994 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649532 | TTACTGCAACCTCTG[C/T]CTCCTCAGTTCAAGC | 5521 |
rs184465584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635345 | AACATGTGTCATGGG[G/T]TTTTTTTTGTGTGTT | 5521 |
rs184475852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948432 | TTGATACTGTTCCTG[C/G]AAGATGGTAAAATTT | 5521 |
rs184483700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036717 | AGCCATTCTGACTGT[A/G]AGATGGTATTTCATT | 5521 |
rs184494064 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070254 | ACCTACTGCCCATAT[A/G]TATTTACTGAATAAA | 5521 |
rs184496803 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882963 | CTTGTCATGGTCCCC[G/T]CCCCCAACACTCACA | 5521 |
rs184500992 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054411 | TAAGTTTTTCTCCAC[A/G]AGGAAGAAAAGATTT | 5521 |
rs184506723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030710 | TCTAATTTATATTAG[C/T]TATCTTACTACTTCC | 5521 |
rs184507841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911030 | TGCCTCATCTTTTAT[A/G]TCATAGTTCAATCAT | 5521 |
rs184513617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651164 | TGTCTTTTCATCTCA[C/T]GGCTTTGGAAGCTAT | 5521 |
rs184515518 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066686 | TTAGACAAATAAGAA[A/C]GATATGGCCCCTGTC | 5521 |
rs184522672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952198 | CTTTCTTGCCCTGTT[G/T]ATTTTTTAAATCCTT | 5521 |
rs184531078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620416 | GCCTCTGAGCACATT[A/C]TCTCCAGCAGGCAGC | 5521 |
rs184531991 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800306 | TTATATAAATTATCT[C/T]ACTTCATCCTCACAA | 5521 |
rs184539569 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934178 | GCAGCATGATTTACA[A/G]TCATTTGGGTATATA | 5521 |
rs184542724 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146878976 | CTCTTCCAACCTCCT[C/T]CCCTCTCGCGCCACT | 5521 |
rs184549583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762654 | GTCAGGCACAGAACT[C/T]GAAGTACAGTCTGTG | 5521 |
rs184559272 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940291 | ATGATTGAAGCGCCA[C/T]ATCTACTTGGCCAGG | 5521 |
rs184564344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894403 | AGCCTATTGTGATTT[A/T]TAGGCCTTGCCAAAC | 5521 |
rs184565124 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887065 | CATTAAAAAGTGAGG[A/C/G]AAAAAAGATGAAATT | 5521 |
rs184568298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831699 | AGGAGGCTGAGGCAG[A/G]AGAATCCTTGAACCT | 5521 |
rs184570099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848973 | TCCACTTTGGCCATT[A/G]GGAGCTCTTCCAGTT | 5521 |
rs184571885 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591218 | AGAGCAGGAACTCTC[A/G]TGTATTTCTCAAATG | 5521 |
rs184579174 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025076 | AGAAAAAAAATTGAC[A/G]ATATCAGAAATGACA | 5521 |
rs184580762 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864773 | GATCAAATTAAAATT[A/C]AATGGCTGTATCTTT | 5521 |
rs184592225 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919490 | CACAGATCAACATGC[A/T]AAAGAGAAAGTGAGT | 5521 |
rs184594793 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970867 | GTTTTTTTTTTCCTG[C/T]AGGAAAATTAGAAAA | 5521 |
rs184598136 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856029 | TTATTCTTCGTTATA[G/T]TCAAAGTAAGATGCC | 5521 |
rs184601256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819564 | GAAAATGTACTATTT[A/G]AAAACTAGCTCCATC | 5521 |
rs184602830 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804833 | ATGTTTAATGCTTCA[C/T]ACTCCATGATGAGTC | 5521 |
rs184606318 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871419 | CTGTCCTACACTGGG[G/T]ATGAGTGACATGGAG | 5521 |
rs184623575 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907643 | GTTTAAGTTCTCTAC[C/T]TGGGAGAAACCCCCT | 5521 |
rs184637968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882339 | AGAATTTCTTTCTTC[A/G]TAGAACTTAAATTCT | 5521 |
rs184642846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667999 | GGACATCCCATATTC[A/G]TAATCACATCCACAC | 5521 |
rs184648230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822685 | TCATTTGCTTTGTGG[G/T]TTCTTCCTCCCACAG | 5521 |
rs184655769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050075 | GGAGTGATGTGCTTG[A/C]GTAAGAGAGAGGGGA | 5521 |
rs184660448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637418 | GGACAGCCCCTTCCC[C/T]GAAACAAAAATCTAT | 5521 |
rs184668270 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853327 | CATAATGATAGTATA[A/G]AGTTCCATGTAGTTT | 5521 |
rs184674115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600529 | TAACATGTTTGGACT[A/G]GCTAGGAAGCTGACA | 5521 |
rs184688267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955925 | CTGGGATTACAGATG[C/T]CCACCACTGTGCCCG | 5521 |
rs184694314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788833 | AACAAAACTCTCTGC[C/T]TTGGGGTTTTGACTC | 5521 |
rs184697104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923722 | TCCCATTACTGGGTA[C/T]ATACCCAAAAGAATA | 5521 |
rs184704947 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761773 | ATAATAATTACAGTA[G/T]GAGGAGATGTTTGTA | 5521 |
rs184709570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986969 | CATATAATAAACTCT[C/T]AAATGTCAAAAACAA | 5521 |
rs184732717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729514 | AATGTCTCCAGGCCA[C/T]GTGAGAGACCTTCAT | 5521 |
rs184753575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624190 | CAATGAAGATAAATC[A/G]ATGAGAAGGGGCTCT | 5521 |
rs184757480 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001283 | ATAAATCTTGCTGCT[A/G]CTCACTCTTTGGGTC | 5521 |
rs184760601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605835 | ACACTTTGGGTTATA[C/T]TGCTATAGTCAAAAC | 5521 |
rs184762477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969896 | GTGAATGTCCAAGTG[A/G]AGATATCCACGAAGC | 5521 |
rs184765725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986681 | AAATAATCAGTGAGC[C/T]TGAAGACAGGCTATT | 5521 |
rs184774848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867944 | GAAAAAATTATGCTC[C/T]CTTGGAGTTTATAAC | 5521 |
rs184778676 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053166 | TCTCAATATCTCTCA[C/T]TTGACATGTAACAGA | 5521 |
rs184779921 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692786 | TGATCCGCCTGCCTC[A/G/T]GTCTCCCAAAGTGCT | 5521 |
rs184781841 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041504 | TCCAGAGTTTCCATA[A/C]CCTGAACTAGACATG | 5521 |
rs184783387 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018007 | TCTTCCAGGCCCAGA[C/T]GAATTATAGTCTACG | 5521 |
rs184787691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638471 | CAGGAACTTGGGGAA[A/G]GGGAGAATTAGCAAT | 5521 |
rs184788841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035932 | GTTGCTTTTTCTCAA[C/T]GGATTTTCTTAGAAT | 5521 |
rs184789756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658660 | AATCAGATCTTCTCA[C/G]GAGTACCCACAGCCT | 5521 |
rs184791621 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076622 | TTAAAATGGTTTCTT[C/T]CCACAAGTCTATTTT | 5521 |
rs184804214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602016 | ATAGAGTATATCTCG[A/T]TATTTCCCACTTCTA | 5521 |
rs184809417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835636 | CTACTGATGAAGAAA[C/G]TGAAGCCAAGAAAGG | 5521 |
rs184811470 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955431 | AGGGCACAGCATTCA[C/G]TTATACAATGTTTTA | 5521 |
rs184823314 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939426 | GTGATGAGCAGAAGT[C/G]AAGCTTAGGCTTCAA | 5521 |
rs184824857 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808380 | CATAGTGTTGTTTTA[A/G]AGAATCCAATTGCTG | 5521 |
rs184840475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982941 | GAAGTGAGTTTCTTA[C/T]AGAGAGCATATTGTT | 5521 |
rs184842066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804401 | GGCAGACCCGGGACT[A/G]GAACCCAAGGCCATC | 5521 |
rs184845384 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784396 | CTACAAAATAGATGT[A/G]ATGAAGAAATATATT | 5521 |
rs184865331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819091 | GGCACAAAATCTCCA[A/G]CTGAAAATCAGCTCT | 5521 |
rs184869452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751149 | CCAGAGAATCCAAAT[C/T]GTGGCATGAGGTACT | 5521 |
rs184869599 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744394 | TTTTTAGATGAAAGG[A/C]ACTTGGCCCTTAGGC | 5521 |
rs184870111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003641 | AGAAAGGGACAAATT[A/C]TCTACCAGTCAGCAA | 5521 |
rs184877871 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711822 | GGGATACAAGTACAA[C/T]GTTGGGGAAAGGTTG | 5521 |
rs184888024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767193 | AACAGGAATACTTGA[A/G]AATATATAAAAGTGG | 5521 |
rs184888981 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918911 | ACTATTTAAATTGCA[A/C]CTTTTCTGCTAGATT | 5521 |
rs184889756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056535 | AAAGCCACAACGCAA[G/T]AATAGAGACTAAACC | 5521 |
rs184894443 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717906 | ATTTCAGCTTGAACA[A/G]CAGCACTTCCTGAGA | 5521 |
rs184897518 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717076 | ATGTAATGCACATGA[C/G]AGCTCTCTGCTTAGC | 5521 |
rs184898398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752144 | TGGTGGCAGCTTGGA[A/C]TAGTGTGGTAGCAGT | 5521 |
rs184901916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733712 | AACCACACACAGACA[C/T]ACACACACACAAACA | 5521 |
rs184903520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734645 | TGGCCATGCTTCTCT[C/T]TCCCACTCTGTCTGT | 5521 |
rs184904503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676889 | GTTTGACCGTCAAGT[A/G]GTGCAACGGCATATC | 5521 |
rs184905185 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865001 | GTTCATACCATTTAA[C/T]CCAGTAAGCTACTTT | 5521 |
rs184907954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698937 | AAGGGTCTGCAGAAA[C/G]AGGAAGAAAAAGAAG | 5521 |
rs184908343 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146622082 | CCCTGGCTACCTCTC[C/G]TACAGGCCTGGGGAG | 5521 |
rs184911890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646022 | ATTCTTCAGCAAAGC[C/T]TTCCCTGGTCTATAG | 5521 |
rs184913831 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951751 | ACATTTTTAAAATCC[A/G]GTCTACCACTGATGG | 5521 |
rs184927958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683324 | ATTCAGATGCATATA[C/T]TAGGCATTCTATTTT | 5521 |
rs184928089 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644295 | TGGGTAAATCAGGAG[C/T]TTTAAATTGTTTTTG | 5521 |
rs184932722 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832551 | TGCCTGCCACCACAC[C/G]CAGCTAGTTTTTTTG | 5521 |
rs184936152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665288 | AGTGTAGCCACCGCC[A/C]CCCATGATCTTAGCT | 5521 |
rs184942128 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649637 | GTATTTTTAGTAAAG[C/T]TGGGGCCTTGCCACG | 5521 |
rs184942273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607900 | AGTGTGAAAGCAGCA[C/T]AGACAATATGTAAAC | 5521 |
rs184946456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046749 | CCCTCACTATTTTTA[C/T]CTGTAAAATGTGGAT | 5521 |
rs184947473 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081357 | TGCTCTGTCTCCTCC[A/G]TTTGACCAGGCCAGG | 5521 |
rs184947827 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886110 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT | 5521 |
rs184950481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007783 | ACTGCGAGGGTCTGC[A/G]GCTTCACTCCTGAAG | 5521 |
rs184954726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028395 | ACCTAGATCAAGAAA[C/T]AGAATGAATACTCAA | 5521 |
rs184963591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021840 | GATTAAGATTAAAAT[C/T]AGTCAATAGAAGCAA | 5521 |
rs184964970 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063339 | AGTTTTACTAAAACA[G/T]CTAAAATTCACTCTT | 5521 |
rs184975567 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081852 | GATGGGGCTAAATGT[C/T]CTGGGTAATAGTGAC | 5521 |
rs184986958 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933755 | GTTACATATGTATAC[A/C]TGTGCCATGCTGGTG | 5521 |
rs184993611 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807876 | ACGATCTCAGCTCAC[C/T]GCAACCTCCGCCTGG | 5521 |
rs185001159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902018 | CAATTCAAAGTGTGA[C/T]GAAAAAATCTCTGAA | 5521 |
rs185011684 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965627 | AAGTGTCGCTGGCCC[C/T]GCTTGCTTTGCGTCA | 5521 |
rs185012736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771006 | CCATGCTCTACCAGG[C/T]GCATTTTGAAAAGCC | 5521 |
rs185018835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736782 | GGATTGCAGCTTTGT[A/G]TTTTCATCCCTGCTC | 5521 |
rs185021540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879777 | AAATCACTAGAAAGC[C/T]AATTTGGAAAAGACA | 5521 |
rs185029477 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703703 | TCACTTTAAGACCCA[C/T]GCAAGTCAAAACAAG | 5521 |
rs185034110 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678193 | AAAAAGCTTATCCAC[A/C]ATGATCAAGTGGGCT | 5521 |
rs185043790 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820526 | AGTGGAATTTTAAAA[C/T]GCAATATAAAAGAGC | 5521 |
rs185058623 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849886 | CCTGACAAACAGGCA[A/C]AAAGCCATGGCAGAT | 5521 |
rs185061768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592721 | TCTTGTGTGAAAAAG[A/T]TAGGACTTTCTTATT | 5521 |
rs185062473 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867018 | TTGTGTTTGTTTCCA[A/C]ATCTCCTGATGCAAG | 5521 |
rs185073020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882088 | CGAGGCCATCCTGGC[C/T]AACATGGTGAAACCC | 5521 |
rs185085836 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788562 | AAGACGAAACCCCGT[C/T]GCTACTGAAAATACA | 5521 |
rs185091067 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800713 | GTACTCCTGCCCTTC[A/G]GTCTAATCAGCTGTG | 5521 |
rs185094914 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822267 | GGAAAGCATAACTCA[A/G]ATTACATCATTTTCT | 5521 |
rs185095827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021372 | GGCAGATACTGGAGA[A/G]GTGAGAGTGGAGAAA | 5521 |
rs185097023 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834567 | AGTGATAATGACTAC[A/C]TTTCCCATATGAAAA | 5521 |
rs185103942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852719 | CAGCAACATGAACCT[C/G]CTTATGTGACAATAG | 5521 |
rs185110527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050647 | GAGGATAACAGTGTT[A/G]ACCTTATAGAATTGT | 5521 |
rs185111705 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814883 | CCCTCTTCCAAGTGC[A/G]CTTTCCTTCCTTTCA | 5521 |
rs185121795 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694898 | CCTAATCATATTTAT[C/T]TATACCAACGTCTAT | 5521 |
rs185127967 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754439 | CTAAGATTGTTAAGC[A/G]AAAAAAGCAAATTTG | 5521 |
rs185136699 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926580 | TAGAGGTTGCTCCTG[A/T]GTCTGTATAGCCTTA | 5521 |
rs185138139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067113 | ATGGTGTTTAAAAAT[A/G]TGTACACATTTTGAA | 5521 |
rs185138914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756111 | AAACCAGAGGCATTT[C/T]CTTCTCTTGACTACT | 5521 |
rs185144567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720728 | GTTCTTTTTGGTGTT[A/G]GAGATTCAGTATTGA | 5521 |
rs185145537 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731703 | ACTTTTCATGAAGGA[A/G]GTGTGCAGATGAAAT | 5521 |
rs185146440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685268 | CTTGGCTTTGCTGTT[C/T]ACTATTTGCAAGGCC | 5521 |
rs185147656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747912 | GACGATACGAAGGGT[A/G]ATATGAACTGAGGTA | 5521 |
rs185150722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660177 | GGCATTGTGTGTACC[A/C]ATTATTGAAGGGTAA | 5521 |
rs185153510 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989211 | CTACTTAAACTCTTC[C/G]AAAAAGCTAAAGTGA | 5521 |
rs185158722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695778 | ACAATCTTATCATCT[A/G]TCTTCATTTTCTCTT | 5521 |
rs185162637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713642 | ATGGTGTAGGCTGTG[A/G]AGGTGAAGAGAACTG | 5521 |
rs185162844 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959047 | GCCTTAATCTAACCA[A/C]AGCCAATATTTTTAA | 5521 |
rs185164056 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680524 | ACAATGTGCACATGT[A/C]CCCTAAAACTTAAAG | 5521 |
rs185176075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661968 | TGGGATTGGGAGAGG[C/T]GGTGGTTTAATTTTT | 5521 |
rs185181513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647959 | CTCATTGTCTCCAAA[C/T]ATATCTCATAATTGC | 5521 |
rs185190835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632601 | TATTCCAGTCAGCAA[C/G]ACAGAGGCTAAGTAA | 5521 |
rs185202250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003094 | TTCTGTACGAGGGAA[A/G]GCAAATGGAGTGAAA | 5521 |
rs185220230 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971143 | ACAAAGAATGCTGCA[A/T]CTTTTCATTGATAGC | 5521 |
rs185222158 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987467 | GTAAACTGAAATATC[C/T]AAAAGACAAAATGTA | 5521 |
rs185230148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784647 | AATATACTATTAAAA[A/G]TGCTAGTTCAAGTTG | 5521 |
rs185237372 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956764 | GAGGCTGGAAGTCCA[A/G]GATCAAGGGGCCAGC | 5521 |
rs185237442 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920645 | GATGGCTTGCTGGTA[C/T]GTGTGTACATGGAAG | 5521 |
rs185245298 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944869 | TCTGGTCTCTCAGAG[C/G]AGTCTAATAGTTTGT | 5521 |
rs185260711 | snp | C/T | 0.029116 | 0.117091 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810865 | TCTCCTAATGCTATC[C/T]GTCCCCCCTCCCCCC | 5521 |
rs185267382 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751300 | AGCGGGGAAGAGGTC[A/G]TAGAGTTCAGTGTTT | 5521 |
rs185267657 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870233 | CAGTGTTATGGACCA[A/C]ATTGTGCCCCCCTCC | 5521 |
rs185268374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917238 | TACACCCTGCCTGCA[C/G]AGGCTGTCTTTGCTG | 5521 |
rs185270492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891753 | TGTAGAGGCATCTAG[A/T]GGAATGAGAATAGCT | 5521 |
rs185276758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717480 | TGCATTGCTTTCTGC[A/G]AAGTTCTTGGGGAAT | 5521 |
rs185282109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975056 | TAGAATGTACCATTT[A/G]AATACAAAGTTCAGT | 5521 |
rs185283652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682622 | CACAGGCTGCCGTCT[G/T]GGCATAGTGAGATGG | 5521 |
rs185289159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940654 | CTTTTCCTTTTCTTC[A/G]TATAAACTTGATAGA | 5521 |
rs185297114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876129 | GAGAAAGAAATCTGA[A/G]AGGTTGATTCTCACA | 5521 |
rs185302352 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963987 | ATTTACCCTTCTCAA[C/G]GCTGAATTTCCTCTG | 5521 |
rs185302556 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950474 | CAAGTTGGCAGCACA[C/G]TGAATCACCTGGAAA | 5521 |
rs185303258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923984 | ACAGGAACAGAAAAC[A/C]AAGTACAGCATGTTC | 5521 |
rs185305003 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854461 | GGCTTCTTTGAAATA[C/T]GCAATACATTGTTGC | 5521 |
rs185307256 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908928 | TGAGTTGCCTCCCGA[C/G]TAGCTGGGATTACAG | 5521 |
rs185308341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932107 | TGGCCCACCCATTCA[C/T]TCAGTAACTATTTAC | 5521 |
rs185319876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060223 | GACTCCCACATACCA[C/T]GTTCCTCTTTTAAAA | 5521 |
rs185321722 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655988 | ACAGCAAAGTATACA[C/T]ATAACGATGGGTAAC | 5521 |
rs185332320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001603 | TGAAGTCAGCGAGAC[C/G]AAGAACCCACCAATT | 5521 |
rs185345307 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824505 | TCATTTGGTTCTTAT[C/T]ATCACAGAAGAGGGT | 5521 |
rs185373859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767780 | ATTAGGGTTCACTCT[C/T]CGCATTGCACATTCC | 5521 |
rs185375911 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734207 | ACTACAGATGCACAC[A/C]ACCATACCTGGCTAA | 5521 |
rs185376769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966440 | GTTGTCAAACTGACA[C/G]AAAGACCTGAGAACT | 5521 |
rs185378243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794619 | CAATAATTCTACAGT[C/T]GAGTAAGCCCAGAAA | 5521 |
rs185392591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997662 | TGCTAAATAATGCAT[A/G]AATATATTCATTATT | 5521 |
rs185406465 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698204 | CCAACTGTAAAACTC[A/G]CCAACTCCCTTTTTT | 5521 |
rs185417034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910333 | TATGAGCTACAATGC[A/C]CAGAATAGGTTACTT | 5521 |
rs185435496 | snp | A/G | 5.61672e-05 | 0.0052991 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878160 | TCACAGGAGAGGGGG[A/G]CAGGGGAGCCAGTGG | 5521 |
rs185448779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043587 | TATGGCAGCCTTAGC[A/G]AACTAATACAGGAGG | 5521 |
rs185453715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642037 | ACCTGACTGCTTACG[A/G]CATTTCTTATTAATG | 5521 |
rs185459276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647439 | CTTCAGTGATGAGAG[A/G]CTCAGTGCTTAGGGC | 5521 |
rs185459970 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018572 | GAATAGGAAATGTTA[A/T]GTATCTAGATTCTAG | 5521 |
rs185462602 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003877 | AGAAAATATACTCCC[C/T]TGTCCCCCAACTCAC | 5521 |
rs185464480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602874 | GCCCCTGGATTCTGA[C/T]TGGTATCTTCATAGT | 5521 |
rs185465111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848383 | TTTCTACTCTAGGAT[C/T]CTACCCAGGATAGTA | 5521 |
rs185465145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795981 | TATAAACATGCCTGC[A/T]TATAGACTATCCCTA | 5521 |
rs185466307 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606503 | ATGGAGATAATAGTA[C/G]TACCTATGTTCTAGG | 5521 |
rs185473200 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632114 | TCCCAGTACTGCAAA[A/C]TATAACTGTATTTGG | 5521 |
rs185474616 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990398 | CAATGGAACAAAATA[C/G]AAAGCCCAGAAAGAA | 5521 |
rs185475213 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991312 | AATAGCCAAGATAGG[A/G]AATCAACCTATGTAC | 5521 |
rs185479225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615611 | AAAAATGATCTCAAC[A/G]GCAAATAATCTCAAG | 5521 |
rs185480881 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954152 | TTTTTTTTCAGTTTG[A/G]GGAGCCATCAGAGCC | 5521 |
rs185481067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968130 | TCTGTTCTGGATCAC[C/T]GACCTGGGCAAAGGG | 5521 |
rs185481541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004812 | AGAGAACAGGAATAG[C/G]TCTTGTGGTCCTTAC | 5521 |
rs185485285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051431 | CTTCTTTCCAGTCTC[A/C]TTGTGGTTTGTGTGA | 5521 |
rs185485507 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977602 | CACTGTTCAACTCCC[A/C]CTTATGAGTGAGAAC | 5521 |
rs185487982 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012900 | CGGTTTTGAGTGAGA[A/C]TCTTAATCCTGAGTT | 5521 |
rs185490217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032505 | TATTTTAGCTCTCAC[C/T]CCCCTCTCCCTCTTT | 5521 |
rs185491070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759740 | GGTGGGTCTGACTGG[A/C]AAATCCATTTCTTCC | 5521 |
rs185492225 | microsatellite | (A)6/7 | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752769 | AACAAAAATGAGCAG[(A)6/7]GCATTGCCTGCAGCC | 5521 |
rs185493267 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067606 | GGAAACATTAAGTGG[A/T]AAAGTGGAAGAGGAA | 5521 |
rs185508361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726479 | ACAATAGTGACCATA[C/T]TTATTGAACAACCCA | 5521 |
rs185523395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010059 | GTACTCATAAATACA[C/T]ACTTTACAAGGGCAT | 5521 |
rs185525694 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912787 | GCTGGGATTACAGAC[A/G]TGAGCCACCGCACCC | 5521 |
rs185527623 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983220 | GAGTCTTGCTCTGTC[C/G]CCCAGGCTGGAGTGC | 5521 |
rs185550118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894044 | GAGTGAGACTCAGTC[C/T]CAAAACAACAACAAT | 5521 |
rs185554226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697530 | GTGCTCCTATCATAG[A/T]AGTTAATTTTTGTCA | 5521 |
rs185554739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946175 | AAAAGGACATACAAT[C/T]AGCTAGTAGCGAGTA | 5521 |
rs185556968 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961020 | CAACTCTTGCCCCAG[A/C]TTTTATCCTCTTATG | 5521 |
rs185564592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663622 | TATACTGTAGTCTAT[C/T]AAGTGTACAATAGCA | 5521 |
rs185564689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069455 | CCCAGAATAAAACAC[A/G]ATTATTTACCATGGC | 5521 |
rs185565212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840320 | GTTAATTACCCCTTG[A/G]AATCTTTTTTTTTAC | 5521 |
rs185571771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929031 | ATCCAAGTGACTAAT[C/T]CTCTCACTTCCTTCA | 5521 |
rs185578952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044980 | ATGTTTACTGCTATT[C/T]CAAACAGAACAGAAT | 5521 |
rs185580925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635073 | TGACTCCTTTGTGCC[C/T]GGCAGAGGGCTAGGA | 5521 |
rs185582360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828614 | AGGCTGTAGAGACAG[C/T]CAGATGGAGATAATA | 5521 |
rs185585321 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925279 | GCTATCATAGAGTAC[A/C]ATTTCCGGAAGGCCT | 5521 |
rs185586888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791152 | ATATATAACACAAAA[A/G]GTAAGGAGTAGAATG | 5521 |
rs185591257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831313 | ACCAGCCTGGGCAAC[A/G]TGGCGAAACCCCATC | 5521 |
rs185597649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844825 | CAATAACCTGTGAGG[C/T]TGCAGAACTTTCTTC | 5521 |
rs185597989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596052 | AAATATTTTAAGCTC[A/T]GTGGGCCGTATGGTC | 5521 |
rs185602277 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589129 | AAAAGCCAAGGAACA[C/T]GTAAGTAGAAGATTA | 5521 |
rs185605597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861211 | CAGGTGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 5521 |
rs185607222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756793 | TCAGTGACTGTTGTT[C/T]GTATGTGCAGTGAGC | 5521 |
rs185610014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864006 | ATTCCTTGGAACAGC[A/G]ATTTTAGAAGGAAAT | 5521 |
rs185610436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801522 | TAAGTGGAGACTGGA[A/G]CACAGAAGATGCCCT | 5521 |
rs185619753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739126 | CTGAGCTCAAGTGAT[C/T]CCCCATCCCCCGAAC | 5521 |
rs185619931 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815375 | TGTATGCTTATTGAG[A/G]GCAGAGAGGCCATCT | 5521 |
rs185622001 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773553 | AATAATGAATTATGG[C/T]CTATCTACAAAAATA | 5521 |
rs185632708 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775746 | ACACAAACACACACA[A/C/T]GCAAATCTGTCATAG | 5521 |
rs185634335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723953 | CTGTTTCATTCATTC[A/G]TGCCAACATTTCCTG | 5521 |
rs185635574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006873 | GATAGTATGAGATGC[C/T]GCCCGGTGTTTACAG | 5521 |
rs185645542 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980714 | ATATTGATTTACAGT[A/G]TCTTTTGCATGTAAT | 5521 |
rs185648453 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687121 | GGGAGAGAGAGGGAG[C/G/T]GATTGATCGATTAAT | 5521 |
rs185649024 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742033 | TTATCTCAGGGGCCA[A/C]TCTGTCTGTGTAATG | 5521 |
rs185654204 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706281 | CAACCATGGCCCTGG[A/T]GGAGCTGGTGCGGCT | 5521 |
rs185658041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671645 | GATACTATAAGTGAC[A/G]GCTGACTTCACTTCT | 5521 |
rs185667829 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890564 | CTGGCCATTACTGTA[C/T]TAGTGTGATAAGTTA | 5521 |
rs185693939 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682369 | GGAAAAAAGAGGAGA[A/C]AGGGATTAACATAAA | 5521 |
rs185697140 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923242 | ATATTTACTCTTCTT[C/T]TTCCAGAAAAACAAG | 5521 |
rs185702349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026451 | AGGGCTAGGGAAAGG[A/G]ATGGATTACAAAGAG | 5521 |
rs185704324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061435 | CAATTTATCCTCACC[A/G]AGATTTCCTCTTCTA | 5521 |
rs185709689 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649474 | TTTTGAGATGGAGTC[G/T]GGCTCTGTCACCCAG | 5521 |
rs185720447 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859872 | TAGATTAGAACATCA[C/G]GGAAAGGAGGTAGTA | 5521 |
rs185723331 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617863 | CCACGCCCAGCTAAT[G/T]TTTGTAGTTTTAGTA | 5521 |
rs185747329 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828407 | ATCAGGGCTGGTGCA[C/T]TGCTTTCAGAATGTT | 5521 |
rs185760383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709824 | GTCTGAAATTGTTAA[A/G]CCCTGTGGTTTAAGC | 5521 |
rs185784815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995225 | CAAGCTATATGTTTC[C/G]ATAGTAATCAGTATT | 5521 |
rs185787300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676017 | CAATCACTCATGGGC[A/G]GATTCACCTTGGAGG | 5521 |
rs185794448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906869 | TGTACATTTAAAACT[A/G]GCACATTTTTTGAAA | 5521 |
rs185802332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872212 | GGGGACCTGGATGCT[A/G]ATAATGAATACTTGC | 5521 |
rs185808062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054776 | ATCCTCAACCCTTTT[C/T]AATCAAATGCCACTA | 5521 |
rs185811457 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874558 | TAATTTTTCTTTGGC[A/G]TAGGTTCTATTGTTA | 5521 |
rs185826536 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826843 | TACATATCACTTCTG[C/T]CTACACCATACATCT | 5521 |
rs185829606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618479 | AAGCCACTAAGTTCA[C/T]TAAGTATGTGATAAT | 5521 |
rs185832241 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840970 | CAAGACAAATATGTA[C/T]TAAACATTAGTGGCC | 5521 |
rs185834626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888236 | CCTCTCCCCAGACCT[C/T]CAGAGCAATATCACC | 5521 |
rs185842369 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857514 | TGTTTCATTTCATAT[C/T]CAGAAAAAGAATCCA | 5521 |
rs185845265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851148 | CAGTAAAGGTTCACA[A/G]TGGTGCCAATCATCT | 5521 |
rs185847310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928703 | TGATCCTTAAACCCT[A/G]GTATACTATACTCAG | 5521 |
rs185850564 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797296 | AAAATCCATGCCACT[A/G]TTGCTAATTTTTTCA | 5521 |
rs185855209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912414 | GGGGAGAGAGTGAGC[A/G]TTCTGAAAGAAAGAA | 5521 |
rs185855551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866098 | AATGGAAGAATTGAG[C/T]AGCTGGGACAAAGGC | 5521 |
rs185856634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776975 | CTACTAAGATGGCTA[C/T]AATTTTTAAAAAGGA | 5521 |
rs185859740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897131 | TGAACGATGCATTTC[A/G]TGTGTTTCTGAGAGA | 5521 |
rs185865740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880571 | GCCTTCGGTTGGAAT[C/G]ATCTTAAAATTGTTT | 5521 |
rs185870385 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932736 | TCTAGTGGCCCAGGT[A/G]GCTGAATCTTCTCCT | 5521 |
rs185871233 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812123 | ACTAGTTCTGTGACG[G/T]GTGGAAGTTTCCATT | 5521 |
rs185880171 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018800 | ATATTTAGTGATGTC[C/G]TCCTGGTGCCAGACC | 5521 |
rs185886683 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996235 | CTAGTTGGCAGACGG[A/G]GAAGCCTTCACAGAA | 5521 |
rs185889376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833164 | TTTCCACATTAGCTC[A/C]TCACTTCAAAATGCC | 5521 |
rs185894778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964182 | TCCACGGCTAAATAC[A/G]TCAGAAAACTGAGAA | 5521 |
rs185897615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727719 | TACCCAAAATCTATT[C/T]TTTTAGCAATGTTGA | 5521 |
rs185907595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691741 | TCTGACCCCCCTGTC[C/T]ATCCTCTCCCTGCTC | 5521 |
rs185918401 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657858 | AGATGCTCCCCATTC[A/C/T]CCTCTCCAAATAATT | 5521 |
rs185930771 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686608 | GAATAAAATCCATTC[A/G]AAAAATTGTATTCAT | 5521 |
rs185936830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900263 | AGTCAGAAAACATAC[C/T]TGAGCCAATCTGCTA | 5521 |
rs185941963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671269 | TATTTATAGAAAATG[C/T]ACTGTGTCAGGCAAA | 5521 |
rs185943716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653370 | TGGTAGTTAAGAAAC[C/T]TCAATTAGGTGTTGT | 5521 |
rs185950113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639990 | ATGGATGAAAGTCTT[A/G]TATGCTTTTCATTAA | 5521 |
rs185950653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635549 | GGCTAGTGTCAGCCA[C/T]ACTGGGCTATGGGGA | 5521 |
rs185951852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015019 | ACACTTCTTGTTCCA[A/T]GGATTTTGGATAAGG | 5521 |
rs185962394 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815743 | ACACACACACTTTAG[A/G]AATCTGAATAGTCTC | 5521 |
rs185963553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057857 | TTTTAGCCTCATTAC[A/G]GGCCTAACAAGGATA | 5521 |
rs185966010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999854 | CATTGGGCCAGACCA[A/G]TGGTTTACATACTGC | 5521 |
rs185969064 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598429 | ACTAATTGTCTAGAA[G/T]ATCTCATCCAGTCCT | 5521 |
rs185969743 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603442 | GAAGCCAGTGCAGCA[A/G]CACTGTAAAGCCTCA | 5521 |
rs185970447 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845505 | TGATCCGCCCGCCTC[A/G]GCCTCCTAAAGTGTT | 5521 |
rs185976052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052114 | CACTATTTGGTTGCC[C/T]TGGCTTCTGTTTGTA | 5521 |
rs185977991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077894 | CTATCTTCAGTTCAC[A/G]TGTATTCATAATGAT | 5521 |
rs185983998 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033115 | TAAATATTAAATACT[C/T]AAATTAAGAATGCAA | 5521 |
rs185984573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950795 | GGTATAATTTCCAAG[A/G]TTTACATGAACAAAT | 5521 |
rs185985369 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781813 | ATAAAGGAAGAAAGA[C/T]GCTAGGAATGAAATA | 5521 |
rs186008476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917753 | TCATAATCTATCTGT[A/G]GCAAGATCTGAGGTG | 5521 |
rs186017937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995486 | CTGAACGTGCAGGTT[C/T]GAATTCAGGAATGAT | 5521 |
rs186023849 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006950 | TCCTCTGGAGTTGGG[A/C]AACATGGCTTCTCCC | 5521 |
rs186024903 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037199 | TAGTTAAATCACAGC[A/C]ACAGGGGCTGTGGAA | 5521 |
rs186026988 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002055 | CCTTGCCTCCTGGGT[A/C]CTAATGCCTGTCAAA | 5521 |
rs186028000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597445 | CCTTTTCCCTACCTT[C/T]GATTCAGCAGTACAT | 5521 |
rs186031047 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981420 | TCTATTACTTAAAGA[A/T]TTTTTTTCTGGCTTT | 5521 |
rs186034342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980752 | TATATGTTGTCAATT[C/T]TTGGAATGTTTTATA | 5521 |
rs186044262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884776 | TATAAGGTGAGAATT[C/T]CCAAAACCAGGTTAG | 5521 |
rs186048246 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722586 | ATAAGAAAAACAGCT[G/T]CATCTAACAGAAGTA | 5521 |
rs186057024 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027182 | TCAGACAAAAAGGAA[C/T]GCATACAATACAAAT | 5521 |
rs186058498 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686051 | AGATTTGGAGTCATG[C/T]GGACTAGGTTTGAAT | 5521 |
rs186059981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861366 | CAGCCTAATTTCCTA[C/T]ATTTTTAGTAGAGGT | 5521 |
rs186073815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068058 | TTTTAAGCTCATTTA[C/G]AGAGAGTTTACTAAA | 5521 |
rs186081801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653169 | GGTTGCCCAGCTACA[A/G]GAAGCATAGCTAGGT | 5521 |
rs186094420 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829008 | AACATAGAGAAGAAC[A/G]GGTAAGTGAGCTGAA | 5521 |
rs186098247 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623014 | TGTTAGATCTCATCT[C/T]ATTCACTCATACATT | 5521 |
rs186113637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850741 | CAGAGTGCTTGTCAC[A/G]GTTGCAATTGTACAT | 5521 |
rs186128120 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796278 | CCAAGTGTATACATA[A/T]CTGTTCCTCGAGTCA | 5521 |
rs186134676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820822 | TCCGTCAAATTGCCA[A/T]CCTAGAGACACAGGA | 5521 |
rs186135310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802186 | AGTCCCAGTTTCACG[C/T]CCCCTTTTCTCGCAT | 5521 |
rs186144271 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032821 | CTGCTATAAACGTGC[A/G]TGTGCAAGTATCTTT | 5521 |
rs186146185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999415 | CCCTGGATGCATATT[A/T]CAATCCACTTTGGAG | 5521 |
rs186148652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832708 | TTTTAATCATTTATA[C/T]CATATTTTTACTATG | 5521 |
rs186149693 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764264 | CAAAAGCCTTGTGGG[C/T]CCACTTTTGAAGGAA | 5521 |
rs186159377 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742161 | ACAGCCGCCGGGGGG[A/C]ACTTTGCTGTGATAC | 5521 |
rs186161530 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776878 | AGATATACAAATGGC[A/C]AATATGTACATGAAA | 5521 |
rs186162885 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768602 | CTTTAGAATATAAAC[C/T]GGCTTTCCACTGCAT | 5521 |
rs186164139 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738224 | ACACAGTGAAACCCC[A/G]TCTCTACTAAATATA | 5521 |
rs186167535 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759949 | TACAATATCATATTT[C/G]TGCCTTCCCATCCTA | 5521 |
rs186175455 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805933 | TAGAATCCAAATCAC[A/T]TGATGGAAAAGACCT | 5521 |
rs186178289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785661 | CAACGGAACTAAAAT[A/G]ATAACTAGCAAAAAT | 5521 |
rs186183306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883951 | AGCTGGTAGGTACTG[C/G]CTATTGAGAGCTGAT | 5521 |
rs186184033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690303 | TCTAGAGACCCTTCC[C/G]TTAAAAGATCGCTTT | 5521 |
rs186186597 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735546 | GAGATTCTAAATCAG[A/G]GCAGGTTTTATATGA | 5521 |
rs186187327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709535 | TACTGGGGAAGCAGG[A/G]GCGGGACAGAGATTC | 5521 |
rs186191742 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051713 | AGTACCAGGCAAGGT[G/T]CCTTATACTTCACTG | 5521 |
rs186193852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704767 | CAGCATCCTACAAAA[G/T]TTCTAGACTGGTAAT | 5521 |
rs186197914 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670536 | AATCTTGCTCTGTGA[C/T]CCAGGTTGCAGTGCA | 5521 |
rs186198826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752421 | ATCCTATCAGTGCTG[C/T]TCATTTTATTTCTCA | 5521 |
rs186208224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055460 | TACCTCTGCAACATT[A/T]TTCTGTTCTTCAGAA | 5521 |
rs186213536 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616349 | TCTTGAGGGATACCC[C/T]GCAAGCACAAGCAAC | 5521 |
rs186214275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593908 | GGCAAAGGGAGGGAG[A/G]CCAGTTATAACCTGA | 5521 |
rs186217621 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639048 | CGTTTTCCTTATCCT[A/C]ATTTTTTCAGGGGTG | 5521 |
rs186218177 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854330 | TTTATGGGGTACATG[A/T]GATATTTTATTACAT | 5521 |
rs186223107 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073301 | TTATGCAAAGAACCC[G/T]CTTCCCTTCCTCCAG | 5521 |
rs186244507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984529 | TTGGCTATTGTGAAT[A/G]GTGTGGTAATAAACA | 5521 |
rs186251393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823658 | TTAAAGTTTAAAATC[C/T]TGGAAATGGATTCAA | 5521 |
rs186288523 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014829 | GCATGGCACATGTAT[A/G]CATATGTAACTAACC | 5521 |
rs186289588 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888483 | TTATATCAATAGATT[C/T]GAACCAGTCTCTGAT | 5521 |
rs186296867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731630 | GCAAAACCTTGGGAG[A/T]GTCAGTCACCCTCAT | 5521 |
rs186299653 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763809 | CTCACTGCAACTTTG[A/T]CTTTATGGACTCAAG | 5521 |
rs186301101 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872656 | GCTAATGTATTTCAC[A/G]AATCACTCAGATCTC | 5521 |
rs186301984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936145 | TAGGCATCAGCAGAG[A/C]CACATATGTTGACAT | 5521 |
rs186302963 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976441 | CATGCCCGGCCAACA[A/G]TTTTATAGTTTTATG | 5521 |
rs186303085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922136 | GGTGCCTAGTTGAGG[A/G]TTAAGTACATAGCAG | 5521 |
rs186309154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078603 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 5521 |
rs186311629 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899996 | TTCAACATTGGTCCC[C/T]AAAAAACAATGAAAT | 5521 |
rs186314113 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904661 | CTGCTTGAAGTCCTG[C/T]AGCCTCAGTATAGAA | 5521 |
rs186322192 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695285 | TATTTTTGTTTTTCT[A/G]TATTTTTTTTTCCAT | 5521 |
rs186335463 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660458 | TAGTGGAGCGTTAAA[C/G]CTCACTTTGGTCAAA | 5521 |
rs186339506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931193 | CCAGAACCTTCCGCA[A/G]TAATACATTGGCAAG | 5521 |
rs186355019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837782 | CAACATTTCACATGC[A/T]CAAGACTCACATATC | 5521 |
rs186368673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883170 | GCATTTATAAATTTC[A/G]TGACCTTTGGTGAGT | 5521 |
rs186375019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869757 | AGAAAGAATATAGTA[A/T]TATTTGACTTATAAA | 5521 |
rs186391546 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042146 | AGCCCCTGCACCTGG[A/G]ACTGTTTACTTTCCT | 5521 |
rs186392134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809830 | ACATGGAGCAGAGAG[C/T]GGAAGCAGGGAGACC | 5521 |
rs186398007 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953924 | AAAAGAGAATTGGTA[G/T]CATCAACTAGTTTGG | 5521 |
rs186402362 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916614 | CCCACAACTAAACTG[A/T]ATTGACTTCCCTCAT | 5521 |
rs186405348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897282 | GGGTGAAAAATGGAG[C/T]GGGTGTGAAAAGGGA | 5521 |
rs186406122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854103 | CAGACACATAGTAAG[C/T]GCACAATAAATACTT | 5521 |
rs186406315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816318 | GCTAGGAGGATGACT[G/T]GAGCCCAGGAGGCTG | 5521 |
rs186410024 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829513 | ACAGCTAAAGGCAAG[A/T]GGCACAGATAAGGTG | 5521 |
rs186411263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899228 | TGGAACCAACCCAAG[C/T]GTCCAAGAATGATAG | 5521 |
rs186411426 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869175 | CATTAGGAAATTCAG[A/G]TTCTTGGTTTAAATG | 5521 |
rs186418357 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708733 | GTACACAGAGTCAAA[G/T]ATTTTTTTTAATCTT | 5521 |
rs186420814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764382 | TGAAAGTTATTATTT[C/T]GCAGGAGTATTTAGG | 5521 |
rs186420895 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781654 | CAAAAAGTATGTATT[A/G]CTTAATCAATACCAG | 5521 |
rs186424494 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675257 | GAGCCACTGCACCCC[A/G]CCGATACTTGGTATT | 5521 |
rs186424943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689221 | TCTTACACAAAATAA[C/T]TTATTGAATCCTCAC | 5521 |
rs186429651 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802823 | CCTTTAACTTGTGCC[C/G]CAAGGCTCAGAAGCC | 5521 |
rs186432689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836969 | AATATGTATTGAACA[C/T]TTGGTTTTAGGTGCT | 5521 |
rs186432980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782074 | CCACCCATGCTCCAG[C/T]GATTTGAATACTGGC | 5521 |
rs186435541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747381 | GTTCAACCTATAATT[C/T]CCAATTTATGCACCA | 5521 |
rs186435849 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920929 | ACCAAAACCTCTTTG[A/G]AGAGAATTAAAATGG | 5521 |
rs186439102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656909 | GCTTTGAGTCTTCCT[C/G]CCTCAGGTTCTTATT | 5521 |
rs186440299 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643768 | TTTAAAAAGAAAAAG[C/G/T]CATATGGTATAATCC | 5521 |
rs186443638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598688 | TTTCCTGTTATATCC[C/T]GCATCAAATTTGTCC | 5521 |
rs186443794 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019590 | TTTGTTTTTTGTTTT[G/T]TTTTGTTTTTTTTTA | 5521 |
rs186446830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626007 | TGAAGAAATTGAGGA[A/G]ACATTCCCCCCTAGA | 5521 |
rs186449003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748754 | CATGGTATGGACGTA[A/C]CACAGTTTGATGTGC | 5521 |
rs186451688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987885 | AAGAAACTCATGTCA[C/T]TTATAAAGACATGCA | 5521 |
rs186453785 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984317 | TTTGATCATCTTAGA[A/T]TCCACATGTAAGTGA | 5521 |
rs186454745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607235 | GGTAAGAACTCCCTC[A/G]GACTGACAATACTGG | 5521 |
rs186455974 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002563 | AAATCCGATTTTTCT[C/T]GGTCTTCTTTGTGGT | 5521 |
rs186457002 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055282 | AAGTTATCAAACAGA[C/G]AGTGACAAAACAGAG | 5521 |
rs186463649 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037637 | GGGATATGTATCTAC[A/G]CCATCTGTAGAATGG | 5521 |
rs186466537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071286 | CTCCCTGCCTCATGA[C/T]TTATTATGTGAAAAA | 5521 |
rs186467797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713127 | GAGGCTGCAATTTCA[A/G]TAGGGTGGTTGTGAC | 5521 |
rs186495044 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653847 | GCTCAGATAAGACAG[A/C/G]GGGGATGGAGAGCTG | 5521 |
rs186497681 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971913 | TGGCAACATCTCATA[C/T]CTCCATGGTACACTC | 5521 |
rs186526913 | snp | G/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768265 | TTTTTGTAGAGACAG[G/T]GTTTCGCTATGTTGC | 5521 |
rs186528295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805484 | ATGGAAAGCAGATAG[A/G]TCATTCCTCATTTAT | 5521 |
rs186533829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742534 | ATTTCTTCACCTCCC[C/T]ACTTTTTTCTGTTTT | 5521 |
rs186536593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002741 | GTCCAGGGACCATTG[C/T]GGGTTCTCGGGCAAG | 5521 |
rs186543559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738701 | TCCTCATGGGCAGAG[A/G]GCACCTTGGTCAGAT | 5521 |
rs186546183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973007 | AAAATGTATTAGTTT[A/C]TCTTATGAGTTATGG | 5521 |
rs186549276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988684 | GATCTGAAATAAACA[A/G]CCTAACATTATACCT | 5521 |
rs186578624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910208 | TCATTTTTCACGAGC[C/T]TAATAACAAGAAGGT | 5521 |
rs186584403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893869 | CATGTATCCCAGAAC[A/T]TAAAGTAAAATTGAA | 5521 |
rs186599310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058377 | TTAAATAAATGGTAG[A/G]CACTTAGCGAATACT | 5521 |
rs186599928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049596 | GATTCCTGGGCTTCA[A/G]TATTTACAGTTTAGG | 5521 |
rs186600570 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022847 | AACCCAGTCTAGATA[A/G]AACCAGTGAAAATAT | 5521 |
rs186602449 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023081 | GAATAACAATGAATT[C/G]TATTATGCCATATGT | 5521 |
rs186606200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684505 | CCTGATTAGATACCT[A/G]GCCCCTCAGAGCCAG | 5521 |
rs186610062 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943627 | AACCATCTTTCAACT[A/C]TTTAGAATGGACTTG | 5521 |
rs186612145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924984 | GCGTTTTAATGTATC[A/G]TGATCTTCTTTTGGT | 5521 |
rs186616489 | snp | A/C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066167 | TAATGATAGTTTTGG[A/C/G]GGAACCATTCAATCA | 5521 |
rs186617300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934984 | CTCCATCAGTTACCA[C/T]TGATTAATTTATGCA | 5521 |
rs186617771 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647222 | TTTTTGACGTTCACT[A/G]TTGCTTAGAAGCACA | 5521 |
rs186633985 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082801 | GATACCCATTTGACA[C/G]TTTGGGCCCTTTAGC | 5521 |
rs186637577 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609143 | TCAATGTGATATGTC[A/C/T]TATCAACAGAATGAA | 5521 |
rs186649802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960162 | CTGACTATAATTCTC[C/T]CTCCTAGGTTCTTAC | 5521 |
rs186650980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998424 | AATTGCCAGCCCAGG[A/G]AGTGGGAGTGACTCA | 5521 |
rs186652819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967464 | TTTATAAATGAGGAC[A/C]CTGAGGGACAGAGAA | 5521 |
rs186698896 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990489 | AAACAGTCCCAATAA[A/T]TGGTGGTGGAAAAAC | 5521 |
rs186701106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904219 | GCCTAAGAAGGAGAA[A/C]AAAATTTTTGAAGAT | 5521 |
rs186711716 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903646 | TAAGTAATCTGCCAC[C/T]CTTGGCTTCCCAAAG | 5521 |
rs186743871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785373 | GCAACATAGTGAAAC[A/G]CTGTCTCTACAAAAA | 5521 |
rs186744550 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624073 | ATGTAAGAAAAAAAA[A/C]CAATCATTGTCAGTG | 5521 |
rs186753553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005557 | CTTGCAAAAACCCAA[C/G]GAGGTGGCAGTCTTA | 5521 |
rs186753587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604725 | ACTATCACTCTTCTC[A/C]TTTGTAGATAAGGAG | 5521 |
rs186757705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969379 | ATAAAGTGCTGAAGG[A/T]AAGGTGGTCACATCA | 5521 |
rs186757919 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042606 | CATTCATCCAACAAA[G/T]ATTTATCATTCACTA | 5521 |
rs186758539 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761144 | AGAAATACCATTTGA[C/T]CCAGCCATCCCATTA | 5521 |
rs186758786 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840573 | CCACACATCTAGACA[C/G]TCCTAAAATACCCAA | 5521 |
rs186763922 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986418 | AACACTTCACCATTG[G/T]CTGACTCAAGTGTCC | 5521 |
rs186767601 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079469 | ATATATATATATATA[C/T]ACATGTGCAATGGAA | 5521 |
rs186769323 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723396 | CACTCACATAAAAGT[C/T]GGAATACTGATAATC | 5521 |
rs186769670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059425 | AGTGGCATTAGTCTC[A/G]GATATACCTAGTGTC | 5521 |
rs186774810 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821241 | CACAAATCCTCAAAT[A/G]CATCAACCCACCTGC | 5521 |
rs186780779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871654 | TAGATCAAGTAAATC[C/T]AGCAGCACCGACCAG | 5521 |
rs186783780 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838248 | GAAATGTGAAATACA[G/T]GGTGGTTAGGGGATT | 5521 |
rs186787056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923045 | ATTTCATTTGATGAC[A/G]TAGGTGAGCCATGTA | 5521 |
rs186792033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753072 | ATTTTGGCAAAAGCA[A/G]AACTAGTACAACCTT | 5521 |
rs186795512 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786243 | CTATTGAGAAGGACT[A/C]ATTTCAAAGGTCATT | 5521 |
rs186796346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793495 | TCATTTAAGTCACTT[A/G]TTTAATCCCTATAAC | 5521 |
rs186796952 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906640 | TTCTTTTATTTTTAA[C/T]TGACACATAATGATT | 5521 |
rs186799383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812066 | CATGCTACAGGGAAC[A/T]GGGCCCAAGAGCTCT | 5521 |
rs186801197 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750298 | CTTTGGTTTTCCATA[C/T]ACATTTTAGAATAAT | 5521 |
rs186803351 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890343 | AGGTCAGGTTGGAAG[A/C]CTTTATGCTCAGTTC | 5521 |
rs186810804 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992791 | ATTTCATTACAGACT[C/T]TTATAGGTGAAAGCA | 5521 |
rs186811293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824117 | AGGAAGCTACACAAA[A/G]TAGGATTTGAAATGT | 5521 |
rs186815940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810314 | GTCTCATATGGTGGC[A/G]GGCAAGAGAAGACAA | 5521 |
rs186816314 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766130 | TTATACTTTCTGTAA[C/T]GTGCTCCTAGCTTAA | 5521 |
rs186817188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955354 | TGGGCCTGAGAATCT[A/G]GATTTCTAACAAGTT | 5521 |
rs186819259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938961 | AATTTTTTGTATTTT[A/T]GTAGAGACAGGGTTT | 5521 |
rs186819531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716505 | AGGAGATCTCGGACA[C/T]CTTTGAGGATCCAAT | 5521 |
rs186822498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733656 | TAGAATTGGCAACCA[G/T]TTTGAGAAGGTCATA | 5521 |
rs186826127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697239 | CTATTCAATTAGCAC[C/T]CTTTAACATGTGACT | 5521 |
rs186826595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773828 | TTGCCATGAGTTTTT[C/T]GTTTAATGTGAATTA | 5521 |
rs186829769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042049 | GATAAGATACTGTGG[C/T]GAGCTATATCCGCAG | 5521 |
rs186841177 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719271 | AGAATTATGTACATA[A/G]ATTTATGCAAAGCAC | 5521 |
rs186850055 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630692 | AGTTAGCTGTGAATA[C/T]GGCTGTTGACATTAC | 5521 |
rs186850531 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681979 | CCACTGCCATTGAGT[A/G]TACATATGGGAGGTG | 5521 |
rs186852757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847109 | ATCATCTAGGCCACC[A/G]TAATCTCTCAACTGA | 5521 |
rs186857822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862663 | AGATCAATTAGGAGA[G/T]ACTTAAAAGATGAGA | 5521 |
rs186858029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909766 | TGTGTTTCAATTAGA[A/G]TAGATTTAAGAGTCC | 5521 |
rs186859519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663353 | ACAAGCATTTACTCA[C/T]GGAAGCATAAACTAC | 5521 |
rs186861185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649129 | TGCTAGTGTAGGTAG[G/T]TAGATAGGGATATAT | 5521 |
rs186863842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068235 | ATTATTTTATTTCAT[C/T]CTCCTGACAAGCCTA | 5521 |
rs186867688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893164 | CCAGCTCACTTGCTC[G/T]GTAAAGACATCTCTG | 5521 |
rs186867865 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877230 | CACAGCACTAGTGCT[C/T]ATGTCAGAACAAGCT | 5521 |
rs186873432 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037803 | TCTTCAGATTCATAA[A/G]AACAGATAATATTAA | 5521 |
rs186874411 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816482 | GGTCATCTTCTATAA[C/T]AGAGTTTATGCGCCT | 5521 |
rs186875700 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774632 | GACCAGCCTGGCCAA[A/C]ACGGCAAAACCCCGT | 5521 |
rs186880359 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946019 | ATTTGTTACATTTGG[C/G]CTATCGATTCTAATT | 5521 |
rs186881782 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062664 | CCTGGTCTGAACATT[A/G]TCTCCCCTACTGTCT | 5521 |
rs186890389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830266 | ATGCCATAGGAATGT[A/G]ATAAGTAAACTAAAT | 5521 |
rs186891968 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004069 | AAGGAAAAGCGAGAT[C/T]GGAGAAAGGCCACAG | 5521 |
rs186892088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794701 | TGATTTCCTTCAATA[C/T]CAAATGCCATTACCA | 5521 |
rs186893028 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657078 | CTAAGTGGGGGTTGG[C/T]GGGTCACAGTGCCTT | 5521 |
rs186895139 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740884 | CCATGAAGCTCACAA[A/T]CACCAAAGGAACACA | 5521 |
rs186903313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758685 | GGAGCTTAATACCTA[C/T]GGGTCAAATGAAAGA | 5521 |
rs186907963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977018 | AACTTCATCTTTCTC[C/T]TTGCTACAGGCCAAC | 5521 |
rs186909809 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627464 | GAGGGTGAAGAATGA[C/G]AGTGGATTTTATGTT | 5521 |
rs186934733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887476 | ATACAAACTGAAGAC[A/G]AAAATATATACAGAC | 5521 |
rs186937535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972537 | ACCAACATGCTGAAA[C/T]CCCGTCTCTACTAAA | 5521 |
rs186955036 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002705 | GCTGCGTCGGTGGGC[A/G]CAACTCTTCTGATCA | 5521 |
rs186980470 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806471 | ATCTTGCTTGTAATA[G/T]AAAAAAAAGAAAAAA | 5521 |
rs186982293 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856988 | GTGATTCTAATGCAC[G/T]TTAAAGTTTGAAAAC | 5521 |
rs186993204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912069 | AAGGTGAAACCCTGT[C/T]TCTACTAAAATACAA | 5521 |
rs187017217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826433 | CCACCCTGAAAATAA[C/G]CTTTTTTAGGAGGAG | 5521 |
rs187025412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945816 | AAAGAATGTTACTGA[C/T]GGTATGCAAGAAGAA | 5521 |
rs187025945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735833 | TCAGGAATAAAGAGT[C/T]ATCTATTGCTTGATT | 5521 |
rs187034055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700489 | GAAATGGTCCTATAT[G/T]TAGCACTCAGCTCCA | 5521 |
rs187044572 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827137 | CCTTGGGACCAAGGA[C/T]ATCATAGGGGCTTAT | 5521 |
rs187057132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880343 | GTAACAGGTGAAGAC[A/G]GGTACAAGTTGATTT | 5521 |
rs187060171 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858867 | ACTTGGCAAGAGTAA[C/G]AATGAGTGACTTTAG | 5521 |
rs187074903 | snp | A/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081578 | AAAGAAAGGCAACAT[A/T]TTTTTTTTAAACTGG | 5521 |
rs187081322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675827 | TCAGTCACTTCTCTC[A/T]CTCTCTCTCTGGCCC | 5521 |
rs187084288 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842963 | GGAGGCCGAGGCGGG[A/T]GGATCACCTCAGGTC | 5521 |
rs187085920 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859606 | ACTTCTAAACCTAAA[A/T]TAAAAGTTTTAAAAA | 5521 |
rs187091503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906265 | AAGTTAAAGAAAATA[C/T]ATTATTAAAATTAAT | 5521 |
rs187094715 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873346 | CTTTTTCATTACATG[C/T]CTGGCTCTCTAACCC | 5521 |
rs187095201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643883 | GGCGAGCTTCCATAA[A/G]GACCATGCAGCAAGT | 5521 |
rs187095880 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681534 | ATTCAGATAATTTCA[A/T]CTGAAAAATTCAGAA | 5521 |
rs187099169 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889746 | AGTGAATTATCAAAA[C/G]TGAGAATAATTTTAG | 5521 |
rs187103142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814307 | TTTCTTCCCTTGTAG[A/C]TCTTCTACATGAAAT | 5521 |
rs187105625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662490 | TGATGCCTGCCTCCC[C/T]GGGGTGCTCTTTTGC | 5521 |
rs187114083 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828019 | AGAGAGAGAGAGAGA[C/G]AGAGACAGAGACAGA | 5521 |
rs187116813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607624 | ATACTTCTTTTACAA[C/T]ATGTCTTTTAACAAC | 5521 |
rs187121299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034085 | CTTCATCATTCTTCC[C/T]CTTGCAAACTAAGCT | 5521 |
rs187122520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025196 | GAGGAAATAGACAAT[G/T]TCTAAGATACAATTT | 5521 |
rs187124204 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633860 | GTCTGCTTCTCCATC[C/T]TTAGGTCTCAGCTCA | 5521 |
rs187127889 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068750 | CTGTAAAAAATTGCC[A/G/T]TCAGTTTTCCTTGGA | 5521 |
rs187128079 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993556 | TGGTGATAGAAAAAT[C/G]TAATAAGGAGTACAC | 5521 |
rs187129387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617498 | ACACCTCTGTACCCA[C/T]AAAAAGACGTCAACA | 5521 |
rs187129942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957723 | TTTGTACATTTGTTG[C/T]AATAACGTTCTGACC | 5521 |
rs187131779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006366 | AATAGCAAAGAATAA[C/T]TGGAATCCCAAACTT | 5521 |
rs187133229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052454 | TCACATTGGTTTGCT[C/T]ATAATGACAAATTAG | 5521 |
rs187135579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594892 | TTAAGAGTGATGATT[C/T]GATCTCTTTTTTCCT | 5521 |
rs187151346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799396 | AAGGTCAGTAAAAGA[G/T]GTGTGAAACCAATTA | 5521 |
rs187151717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048141 | GTTAGAGTTGTGTGC[A/G]TATGCATTTTTCCCT | 5521 |
rs187153252 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699600 | GGCAACATGCTGCCT[C/T]GGGTAATTTATGCTA | 5521 |
rs187155104 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081994 | TGGATAGCAGGGGTG[A/C]CAGTTTTCTTCTCAA | 5521 |
rs187158334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019785 | TAAGAGATGTTAAAG[C/T]CATCACTTAAAGATG | 5521 |
rs187160192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665911 | GAGCACATGCTGCTC[A/G]AAAAATGGTGCTAAT | 5521 |
rs187165971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045514 | CCCAGTGATGAAAGT[A/G]CCTAACATGCATTTC | 5521 |
rs187167685 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988134 | AGCAAATATTAACAG[A/G]CCTAAAGGAAGAAAT | 5521 |
rs187173485 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635852 | ATATAATGTGACCAA[A/G]TCAGATTCAGTTCTT | 5521 |
rs187193729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928354 | GAAATCTAAAGGACA[C/G]CTCTAAGTCACCATA | 5521 |
rs187202782 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979415 | ATATAAACTCTGTAA[C/T]AGCAAAGAAATTTAC | 5521 |
rs187208791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896026 | AATAATATTGTCTGA[A/G]TGGTCGCCTGGCTCT | 5521 |
rs187214174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655683 | GACTCAGGAGTCTAT[A/G]CCCTTAGTCGCTTAA | 5521 |
rs187214330 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641934 | CAAAAGCAAAACAGA[A/G]CATTGAATTCATGGC | 5521 |
rs187224566 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624425 | TCTACATCTTTTTTT[A/T]AAAAAAACAGTTCTA | 5521 |
rs187225476 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959998 | ATAGGTTTTAAGCAC[A/G]GAAATGTCATGATCA | 5521 |
rs187229269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605918 | ACGTGTTTTCTGTTA[C/T]AACATGTACAGATAT | 5521 |
rs187239293 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865513 | TATTCATATTCACGT[A/G]TGTTTTTTAACGTAT | 5521 |
rs187243827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841456 | TTTGCATTTTCTGAT[C/T]GTGAAAATTCCTCAT | 5521 |
rs187265133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812866 | ACCATCAGATTGTGT[A/G]AGACTTACTCACTAC | 5521 |
rs187268715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146924028 | CTAAATGATGAAAAC[A/G]TATGGACACATAGAG | 5521 |
rs187271890 | snp | C/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949066 | ATAATAACTTTTTGC[C/G]TGAATAGGTCAAGGA | 5521 |
rs187306073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957228 | GAGTCTTATTTAAAA[A/G]TGCAGATTTCTAGAT | 5521 |
rs187315258 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753482 | TCACCAAAGATGGAC[A/C]CAGTAAATAAGTAGA | 5521 |
rs187320393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861735 | CAATATATTTTTGTT[A/G]CCATTTTTCCATGGA | 5521 |
rs187324797 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769975 | CAGATTTATCAAAAC[A/G]ATGTTTGTCAGCATT | 5521 |
rs187330595 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719628 | TCACTCATCTGGATC[C/T]CAGATAAGGCAGAGC | 5521 |
rs187331799 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718310 | GGAAGACAGATTGAG[C/T]CCAGGAGGTTGAGGC | 5521 |
rs187332549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892634 | CTTATGGTTCCTCAC[C/T]GCCTAGTGTAAAGTT | 5521 |
rs187338450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736233 | TTTCCTGAGGCCTCC[C/T]CAGCCATACTGAACT | 5521 |
rs187338658 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064603 | TAAAGAAGAACTAAG[A/G]TCTGTGTGTAATTCT | 5521 |
rs187341641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683679 | CCAATGAGCAGAACA[A/G]AAACATCCCAAACTC | 5521 |
rs187345091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700940 | CAGTTTTTAGTTTTC[A/G]AGCAAAGCAGCAAGG | 5521 |
rs187352483 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827694 | CATTTATATAATAAG[C/T]ATTGATAAAGTATCG | 5521 |
rs187354389 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813223 | ATAAATCTTAGCCTT[G/T]TAATAATCATTAAAA | 5521 |
rs187365000 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779494 | AATGACTGCCGGCCC[A/G]GTGATAAGGCCGGTT | 5521 |
rs187365590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649845 | AGAAATTATTAATAT[A/G]AAGAGGCATGATGGG | 5521 |
rs187371242 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761679 | CTGTCTGGATTTTGT[A/G]GTCAGATTGCCTGAG | 5521 |
rs187374167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809199 | AGCCTTCTATGTGGC[C/T]GTCAGGCTTTCTGCT | 5521 |
rs187381728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619238 | CCCTATAAAAGGGGC[A/C]GTTTCCACCTGAGGT | 5521 |
rs187384060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798369 | CAGCTGGTAATTTAT[C/T]TCTCTAATCCACAGC | 5521 |
rs187400429 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744220 | ATCCCCTGCCCCCAC[C/T]CTTTTAAATAAAAGA | 5521 |
rs187411792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711475 | ATTTTAGAATGAGAT[A/G]CATTGCTCAATAAAT | 5521 |
rs187421132 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728532 | AATACTTTGCTCTCC[A/T]GTCTTCGTGTGGAGC | 5521 |
rs187421992 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772904 | CCATATCATTTAAGG[G/T]TTTTGATTGTCTAGC | 5521 |
rs187436012 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897927 | AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5521 |
rs187437238 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076568 | TCAGAAAAATAAAAG[A/C/G]ATAAACATTATGTTT | 5521 |
rs187457725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968771 | AAATAAGACCATCGT[G/T]GCCAATTTCAAGCTA | 5521 |
rs187458931 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620243 | GGCTTAGGGTTCGCC[C/T]GTCAATCTAAAGACT | 5521 |
rs187459329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946980 | AAGGCTCAATCCTGC[A/T]TCTTGTTTTATGTTG | 5521 |
rs187459551 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867055 | TTGTTAGTTAATTAA[A/G]TATCATGAAAGGTAA | 5521 |
rs187462268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930243 | CAGTCAAGCAAGGGT[C/G]TCTCTGGAGGGACAG | 5521 |
rs187463576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985241 | GGCCAGGCTGGTCTC[A/G]AACTCCTGATCTCGT | 5521 |
rs187465227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963442 | CTCTGCCTCACCACT[C/T]ACTGGCTCCTACCTG | 5521 |
rs187465809 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882160 | CACGCGCCTGTAGTC[A/C]CAGCTACTCGGGAGG | 5521 |
rs187467032 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954697 | GAGAGCCGAGATCTT[C/T]AGAGAAACACACGCA | 5521 |
rs187470950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909335 | TTCTGGGATATTCTT[A/G]GATTTTTATTCCAAC | 5521 |
rs187473727 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965794 | AATCCATAGCAGGAA[A/C]GCATGATGGTTAATA | 5521 |
rs187474674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146913718 | TGAGGAACGCTCTCT[A/C]ATACCATAAATATAC | 5521 |
rs187494153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933792 | ACCCACTAACTTGTC[A/G]TCTAGCATTAGGTGT | 5521 |
rs187497135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852724 | ACATGAACCTGCTTA[A/T]GTGACAATAGTATAG | 5521 |
rs187512734 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019885 | TATGGGAATACACCG[C/T]TCAGATCTCGTTTCA | 5521 |
rs187512843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055808 | CATAAGGATTCTCTC[A/G]GCCTTTTAAGCTGGC | 5521 |
rs187519594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997464 | CACCCATGGACATGG[A/C]CTTTCAGCTGTGCCT | 5521 |
rs187540058 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877697 | GCGAACATCTCGGGG[A/G]AGGGGTCATCTGCCT | 5521 |
rs187564850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847520 | CTGGTACATAGGTGC[C/T]TGCCTTGCAAGGGAA | 5521 |
rs187569893 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942394 | GTTCTTTTCTTATAC[C/T]GTCAGAAATAAGTCA | 5521 |
rs187577363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592563 | TGAACTACCAGGGCC[A/G]TTGGCCAGGTCTCCA | 5521 |
rs187583171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684053 | ATCTAATCCAGGAGC[C/T]GTTGGTGCCATTGCA | 5521 |
rs187590141 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876903 | CTCTTTTACTCCCCC[C/T]ATCACATTTCTCTAG | 5521 |
rs187592680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818150 | CTGCTAGGAGTTTAT[A/G]TACTCCTTTTGTGAC | 5521 |
rs187593988 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666745 | CTCCACAAATGCTTT[C/G]CTTCACTGAACACAA | 5521 |
rs187598444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650241 | AACCTGAACTCTAGG[A/G]TCTTATCCTATTGTT | 5521 |
rs187603149 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008942 | AGTGATATTCACATC[A/G]TCCTTAGATTGCACC | 5521 |
rs187608636 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783882 | CTGTGCTTCTGCCTC[A/G]GAGAATGATGTTATT | 5521 |
rs187609955 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636274 | AGGGGAGGATATGGG[A/G]GTATACTAAAAAGTA | 5521 |
rs187612182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029911 | TCTGATATTCTGTTA[C/T]GGCAGCCCCAGCTGA | 5521 |
rs187613579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997204 | ACCCAGCAACAATTG[C/T]GGGGTTTCATGGAGC | 5521 |
rs187615317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619404 | AGAATTGCTTGAACC[C/T]GGTAGGCGGAGATTG | 5521 |
rs187620016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599178 | TCTTCCTCTTTCAAC[A/G]AAACCACCCTATACA | 5521 |
rs187624644 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846549 | TGGGCATGGTGGCAC[A/G]TGCCTGCAACCCCAG | 5521 |
rs187624797 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048540 | CTATCCTTAGTTATT[A/G]CTGTGGTGAATGCAG | 5521 |
rs187636091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757498 | AAAGGAAAATGGGTG[A/G]AAGGCGAGAGATGGA | 5521 |
rs187641936 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933719 | TAAGTTTTAGGGTAC[A/G]TGTGCACATTGTGCA | 5521 |
rs187642669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069141 | AAAATTGCTTTTGGG[C/T]GCTGAACAAAACTGT | 5521 |
rs187648189 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823211 | TTCTTCTTCTTCTTT[A/T]TTTTGAGATGGAGTC | 5521 |
rs187649035 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724802 | TATCTGGGAGTTACA[C/T]GCAAACACATTTTAC | 5521 |
rs187650402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687447 | TAGCTAGTGCAGATA[A/G]AGAGTGCAGCGTGGT | 5521 |
rs187661274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756302 | TCTTAATTATCCTTT[C/T]TGATGAGGGGACAAT | 5521 |
rs187662490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635005 | TATGTCTGCAGGCCT[A/G]GAACCGGAGGAATCC | 5521 |
rs187665474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655066 | CAGTCCTTGGCCTGT[C/T]TGCAGGTGGTTCTGT | 5521 |
rs187669117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790465 | CTGGGGGGTTGGCAC[A/G]GGTGAGGGCAGCTCT | 5521 |
rs187669471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965349 | CCCCAGAATCACACT[A/G]TCATTTACTTGTTCA | 5521 |
rs187669756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982243 | TGTTGCCAGGTCCCA[A/C]AATTTTTGATATGTT | 5521 |
rs187681221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951431 | ATGTGCCATGGTGAT[C/T]TGCTGCACCTATCAA | 5521 |
rs187681855 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001153 | GTAAAATGGACCAAT[A/C/T]ACCAGGGTGGGTGGG | 5521 |
rs187684845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728185 | AATGATTTCCCAGCA[A/G]AAGGAAAGCAAGGAC | 5521 |
rs187690472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074082 | TTGTGAAATACACAG[A/G]TCCTTTGACTCCATC | 5521 |
rs187699395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710972 | CATATTTTGGGACTG[A/G]CTCAGGTATCACTTC | 5521 |
rs187700191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637173 | ACCTTTCCATTGTAC[C/T]CCTCAGAGTTCTTTA | 5521 |
rs187704356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676237 | CAGAACATTTAGCTA[A/T]CTGGGCAAAGTAGGG | 5521 |
rs187704551 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035068 | CAGCTCATTTAACAT[C/T]ATTCCCAGAAGGAAG | 5521 |
rs187709843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692204 | GAACAAATCTCATCT[A/G]CCTGCATAGTACATA | 5521 |
rs187714111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657930 | GTTTGGTGGGTTCTG[C/T]ATCATCAATTAGGAA | 5521 |
rs187720727 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834333 | ACTTGACTAAAGTTA[A/C]AACTAGTTAGTGGCA | 5521 |
rs187724718 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600186 | AATGTATCACCATGC[A/G]TTGCCTTCCATTTTG | 5521 |
rs187725405 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620774 | CCCTCCCTCCTTCCC[G/T]CTCATAATTTGTTCC | 5521 |
rs187729427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002832 | ATTGCAGGTTTTTGC[A/G]CAGGGGGAGAAACAA | 5521 |
rs187730743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852646 | TGTGCCAAAAGATTG[C/T]GTGACCACCTCTCTC | 5521 |
rs187731256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600611 | AATAGAGAACTGTCA[A/T]CTCTCTGGTAGCGGA | 5521 |
rs187731433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644687 | TTTGGGAAAGTCATT[G/T]TATCTCTCTGGGTTT | 5521 |
rs187733662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866858 | TAGCTGACACTCCAA[C/G]AAGAAAAAGTGCCTT | 5521 |
rs187734153 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040442 | AATTTGGAGGAGGCT[C/G]TTCCCAGCAGGTACA | 5521 |
rs187736258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020907 | AGTTCGAGAACTGTA[C/T]AACTAAATTTTCCAG | 5521 |
rs187737292 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628731 | TGTACTGGGAACCTA[A/C]TATGTGTCAGGCAGT | 5521 |
rs187741170 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951817 | ATAGTGTAGCAATGA[A/C]CCTATGCATACATGT | 5521 |
rs187741371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946463 | AAGGCAGTGCAATCA[A/G]TAGTGTTACTTTTCT | 5521 |
rs187743180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075756 | AATCTAGCCTATTGC[C/T]TCCAAAACATGCCTG | 5521 |
rs187746202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055919 | CATTTTGCCATCAGC[A/G]CCAGGAAGCACTGCC | 5521 |
rs187751454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788010 | ACTGTCTTTCTCATG[C/T]CTGCTTTCGGAGGCA | 5521 |
rs187754602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009854 | ATATTTATATATATA[A/C]ACACACACATACACA | 5521 |
rs187762601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807615 | TATGTTCATTTCACA[A/G]ATGAGAAATGTGGAT | 5521 |
rs187763478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983162 | TTTGGTTTATCTATC[A/G]TGTTTTCCAGAGCAT | 5521 |
rs187765751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822151 | CAAGAAAAGAAAGTT[C/T]GTAAAATAACAAATT | 5521 |
rs187768450 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039254 | CTGTTTTTATGTTCC[C/T]AGCCCTTATCACTAT | 5521 |
rs187778575 | snp | G/T | 0.00120943 | 0.0245612 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978219 | CCCACTTTTTGATGG[G/T]TTTTTTTTAATTGTA | 5521 |
rs187781268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989078 | AAAACTGAACAGACC[A/C]ATAATGAGCAATGAG | 5521 |
rs187784669 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855392 | TAATGCTAACATTGC[A/C]TAGTTCCCTTAGGAC | 5521 |
rs187788845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770681 | TGAGGGAGCAAGTAA[A/G]TCTGCTATGTGGGTT | 5521 |
rs187795189 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754133 | CACGTGTCAGATGAA[A/G]GATGATTGGAAATTA | 5521 |
rs187801590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885904 | ATGATTCCATTTATG[C/T]GAAACGTTCAGAATA | 5521 |
rs187816325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824787 | CAGTGGTGCAATCTC[A/G]GCTCACTGTAACCTC | 5521 |
rs187835759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863343 | TCTGATAGTTCAGGG[A/T]TCTAGGGAAGCTCTT | 5521 |
rs187839187 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803890 | ATAGTTAAGCTGGTT[A/G]GGCACGGTGGCTCAT | 5521 |
rs187843907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804323 | TCTCTGTTTTTAAAG[A/G]TGAGAGGAATCCGAT | 5521 |
rs187860886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830845 | CTATCATTTCACAAA[A/G]CGATTGTGGTACAAT | 5521 |
rs187862381 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765466 | AGAACAGTGCCCAGA[A/G]CATGGAAGGAGCAAC | 5521 |
rs187886504 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732875 | GGCTTATAGATGTTA[C/T]ACAACTTGTTCAAGA | 5521 |
rs187902832 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679080 | AAAAAGAGCCCGCAT[C/T]GCCAAGTCAATCCTA | 5521 |
rs187908293 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740233 | CAAGTGAAAGAGGTG[C/T]ACAAGTGATAAAAGA | 5521 |
rs187913245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696615 | AGAAATTGAAACAAA[C/T]TTATGTGGTTTGGCT | 5521 |
rs187917367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725300 | ATTAGATTTGATTTC[C/T]TTTGCAGTGATATAG | 5521 |
rs187918277 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964515 | AAGTTCTCAGCTCCT[A/G]TATTTATTTTTATTT | 5521 |
rs187920701 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706553 | GGTCTGCTGAAGGGC[G/T]GCCTCCAGCTCGGAC | 5521 |
rs187931279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706800 | CCTCAGCCCGACTGC[A/G]GTTGGCGATCTCCTC | 5521 |
rs187943285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901068 | TCCATGTCTTTGCTA[C/T]TGTGAATAGCAGCTA | 5521 |
rs187946637 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674298 | TCATACAAAGACAGA[A/G]CTAGGATATGAACCT | 5521 |
rs187948704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687974 | ATTTCAAGAGGAGAG[C/T]GTGTTAGTAAATTAT | 5521 |
rs187951296 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672917 | TAGAAAATGGGATAA[A/C]CCCAGATCCTGAGAT | 5521 |
rs187952299 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732451 | ATAGAAAGGAGGCAT[G/T]ATTTGGAATTTCCAC | 5521 |
rs187958910 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640436 | CCCCTCAGGAGGAGG[C/G]TCTAGGCTGCAGCTC | 5521 |
rs187964785 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044120 | CCTGAAGTCACAGGG[C/T]CCTGCTTGAAGGAAT | 5521 |
rs187967204 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641695 | GTATCCTCTAGAAAC[A/C]CAGGCATTTTCCCCT | 5521 |
rs187970360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831421 | AGAATCACTTGAACC[C/T]GGAAGACTGAGGTTG | 5521 |
rs187972605 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080454 | TGTAACGCAGACACC[A/C]TTAGGGAGAGTCATG | 5521 |
rs187972695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603727 | TAATACTGCAGGCCC[C/T]GTGCTTTACATGTTT | 5521 |
rs187972999 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870365 | TCTTATGGGGCTGGT[A/G]CCCTTGCAAGAAGAA | 5521 |
rs187974872 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951195 | TGTTTTTTTTTAATA[C/T]CAGCTTTATTGAGGT | 5521 |
rs187979321 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933377 | GAGCAGGTCAAAGCT[A/G]CACCTTAATTATTTC | 5521 |
rs187982707 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885497 | AGGATGTGGCAAAAA[G/T]CAGAACCTTCAAATC | 5521 |
rs187984544 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848718 | CTCCTCCAAACTGTA[A/C]TCTGCACCCTTAGAA | 5521 |
rs187984770 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918417 | AGTTGATGATAATGG[A/C]AGCTTGCATTTATTG | 5521 |
rs187998257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954999 | ATGAATAACTTATCT[G/T]CTCGATGGTCCTCCC | 5521 |
rs188003844 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017969 | TGATAAAGACAGGAC[A/C]ATGTAGTTTTGCATG | 5521 |
rs188007854 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052889 | GCAGGCGTGAGGGCT[C/T]AGAGTGAGGGAGGGG | 5521 |
rs188014288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015917 | CTCTTCCTTGAAATA[C/T]GAGTATATTATTTCC | 5521 |
rs188016404 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854718 | GTACCTCACACTGAT[A/C]GCTAAGCTGTGCACA | 5521 |
rs188019680 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985919 | TCTATACAAAAACAA[A/C]AAACTATACAAAAAA | 5521 |
rs188028259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929558 | ATTGATTGGGAAATG[A/G]TGGATATAATATACT | 5521 |
rs188056544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961514 | AAAAATTAGCACCAC[A/G]TTGTTATTTTAATAT | 5521 |
rs188058108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922796 | GATCAGTTAAAATCA[C/G]AAGACTCAGTTCAGG | 5521 |
rs188074085 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871096 | TTCAGCCTGATTCTA[G/T]AGTTCTATTGGAGTC | 5521 |
rs188085855 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834012 | CTCTAAAATGTCCTT[A/G]GCAAATGTTCTTACT | 5521 |
rs188088659 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924456 | TGTGAAGGATGGGCC[C/T]TTCCCAAGTACTGGA | 5521 |
rs188089264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646134 | GTATTTGATGAACAT[C/T]ACTCTGAAAGCGGCA | 5521 |
rs188089344 | snp | A/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855985 | TAGATCTATTTTCTC[A/G/T]TTGGAAATTACCTGT | 5521 |
rs188095107 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021867 | GCAAACTCTAAAAAT[G/T]ATAAGGATGATGGAT | 5521 |
rs188095916 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871314 | GTGGCCCAGGCAACT[A/G]TATGAGTTGTCATGA | 5521 |
rs188100699 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866313 | ATTATTGTATTGTAC[A/G]TCAGTTTGCTCTTAA | 5521 |
rs188102415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839134 | GATATCATGTGCCTA[C/T]CTAGTCTATTCGATC | 5521 |
rs188103873 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886121 | AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 5521 |
rs188105287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629608 | CATCTCATGGTTTCC[C/T]ATCTCACTTAGAGTG | 5521 |
rs188105504 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989619 | AATAAAGGCCTTACA[A/T]GACAAAACCAGAGCT | 5521 |
rs188106826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807112 | TCCACCCAGACCAAC[G/T]GAATCTGAACTTGCA | 5521 |
rs188107881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785649 | TACAAAGGCAAGCAA[C/T]GGAACTAAAATAATA | 5521 |
rs188111262 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608741 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 5521 |
rs188111860 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768282 | TTTCGCTATGTTGCC[C/G]AGGCTGGTCTTGAAC | 5521 |
rs188113006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003756 | GAAGGACTAAGGAGA[A/G]TTAGGAAAAAGCCCA | 5521 |
rs188115976 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811231 | TCTTGATCTCTTGAC[C/T]TTGTGATCTGTCCAC | 5521 |
rs188120419 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825579 | ACTATAAGTGTAAGG[A/G]TTAAAGAAATACTTA | 5521 |
rs188124065 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839690 | TCCCAAAAAATCATC[A/G]GCAACTTGGAGAGTC | 5521 |
rs188128774 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779934 | GTTACATATAGGGGA[C/T]GAATTTTGGTTTATG | 5521 |
rs188138645 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744523 | TGGAAAACACTGCCC[G/T]TCCAGCAGTGAGAAA | 5521 |
rs188142548 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711826 | TACAAGTACAATGTT[A/G]GGGAAAGGTTGTTCA | 5521 |
rs188145240 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945511 | GTCCAAGTCCGATAT[A/G]TTGACTACCTTGCTC | 5521 |
rs188147123 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752218 | GAGATACTGTAGGGT[A/T]GCCTTGCACTTGCCT | 5521 |
rs188147302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795427 | GCCAAATGAAATGAA[A/C]CACACACAGAAAGAC | 5521 |
rs188150879 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749917 | TCCTTTTTTTTCTAA[G/T]AATTTTATAGCTTCA | 5521 |
rs188151486 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928117 | TCAGTCAAGGCTTGG[C/G]GTTGGTTTCCTGAGG | 5521 |
rs188153973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734697 | CATCTTTCAAACTGA[A/G]ACCCTCTGCTGTCAA | 5521 |
rs188155457 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911872 | CTTCCTATACTTAGG[A/G]TTTTTTCAGCACAGT | 5521 |
rs188156440 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676923 | TTGGGACTGGTGTGG[C/T]GGTCACCTCTGAGTC | 5521 |
rs188161392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783366 | TAAGCCCTGATTTCA[C/T]TTAAAAGATATATGC | 5521 |
rs188162169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976260 | CTCCTGCGTCAGCCT[C/T]CCGGGTAGCTGGGAC | 5521 |
rs188181336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059819 | ACCATTTCTGCCCTG[C/T]CAAGTCCAGCTAGAG | 5521 |
rs188184022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715144 | ACTCTCATCCTTTCC[C/T]TGTGCAAGATTTACA | 5521 |
rs188184687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959938 | ATCATATTTCCCAAG[C/T]TAAGCATTTTGAACC | 5521 |
rs188195978 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681045 | TCTCTGGTAAGGACT[A/G]GTATTTAAAATGCTT | 5521 |
rs188211358 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648066 | CTGTGTACCAAAACC[A/G]GGTCTTTTTATCCTG | 5521 |
rs188225348 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616917 | TGAAGAAGTATTTGC[A/G]CTCCCGTGTTTGTTG | 5521 |
rs188235936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993179 | AACTCGTAATCTCAG[A/G]TGATCCACCTGCCTC | 5521 |
rs188237875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962203 | GTGAAGCACAATACA[C/G]TTGTTTTTTTCTTTG | 5521 |
rs188249459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623633 | ATGTCAGAATATGCT[A/C]TTTGACCCTGGGATT | 5521 |
rs188255484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024722 | TTCTAAATAACCCAG[C/T]GGCTCAAAAATGTCA | 5521 |
rs188262152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060442 | GACCAGCCTGGGCAA[C/T]AGGGTGAATACCCAC | 5521 |
rs188272707 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969316 | GGACTGGAGTGAAAC[C/T]AGATCACAGAAACTT | 5521 |
rs188282368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937806 | TTTATGTCTGTTTGG[C/T]TTCTGTATGTACAAT | 5521 |
rs188283837 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936785 | TTGCCAGGTAACTGG[C/G]GATCATAGAAATAAA | 5521 |
rs188290918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000868 | ACTGATTTCTTCAAC[A/G]CCTAAGGGGAATCTT | 5521 |
rs188297684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906119 | AAAGATATATTGTCT[A/G]AGTTGAGATATGTTG | 5521 |
rs188326356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853594 | CAAAACCCTAATTGA[C/G]TAACTAATGCATGTA | 5521 |
rs188331310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656761 | TGGAGAAGATGTTGG[A/G]TCAGTAGTCAGGGCC | 5521 |
rs188331736 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822410 | TTGTCTGTTTCAGTC[A/T]TCATACTCAGGTTGC | 5521 |
rs188337166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044511 | TTCTTTCTTTCTTTT[C/T]TGTTTAAAAAGTGAA | 5521 |
rs188339123 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881133 | AAGACTCACTGGCCA[C/T]TTCTCTTTTCCTCTA | 5521 |
rs188340356 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146868980 | CAGTATCAGCCTATA[A/C]AAGTAAACTGGATTA | 5521 |
rs188341962 | snp | A/C/G/T | 0.00159649 | 0.0282165 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873126 | CCGCTTTTAGTGATG[A/C/G/T]GCCCCATTATGCATC | 5521 |
rs188343650 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643312 | GGTGCAGGAGATACA[C/G]TAGTGACCAAAGCAG | 5521 |
rs188346303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882983 | CAACACTCACATACC[C/T]ACTCTTCCTTCCTTA | 5521 |
rs188347689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625739 | GGAACCTGGGAATAT[C/T]TTACCTTACATGGCA | 5521 |
rs188355395 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002196 | GACTCTGTTACCTTC[C/T]TTAGGCACCTGGGCT | 5521 |
rs188355413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061076 | TGGTTAGTTCATTTA[C/T]CCATTCATTCATACA | 5521 |
rs188359067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788592 | AAATATTAGCCAGGC[A/G]TGGTGGCACATGCCT | 5521 |
rs188359313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606817 | TTTCAATGTCACCCC[C/T]ACCCTGGCTGTGATG | 5521 |
rs188365616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147081202 | TTCTTAAGAGACCAA[C/T]AAGAAAAGAAATATA | 5521 |
rs188368803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851779 | CCTTGCTCTTTAAGA[C/T]GCATATCTCAACAGA | 5521 |
rs188376432 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842234 | CTTCATGGGAATTCA[C/T]AGTCCAAAATTATAT | 5521 |
rs188394427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761867 | CTGGCTTGATGAGGG[A/G]TAAAAAAAGATGGGA | 5521 |
rs188396891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787488 | GCCACCAGAGCTCTT[C/T]CTTCCTTTCCTCTCT | 5521 |
rs188402555 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821960 | TGACAACGTAAGTAA[C/G]TGTGTTCAGAACACA | 5521 |
rs188409580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006603 | TCATTATCCTACTAC[C/T]ACACTCTCAGAGGAT | 5521 |
rs188409626 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971173 | CATCATAGATTTGGT[A/G]AAATGTGGTAGGACA | 5521 |
rs188415341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987504 | AGATGAGTTAAAGAG[C/T]TTTATTTTTTGTTTC | 5521 |
rs188417357 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729522 | CAGGCCATGTGAGAG[A/C]CCTTCATGACAGCCC | 5521 |
rs188425647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692616 | TCAGCTCACTGCAAG[C/T]TCTGCCTCCTGGGTT | 5521 |
rs188428262 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698495 | TGCATCCTAACAGAT[G/T]CTGCAGTCACCCTTT | 5521 |
rs188436631 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682906 | CTGATCTATACAGAA[A/C]CTTGAGGCAGGAGGA | 5521 |
rs188444808 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725868 | GCCCATGTCTGTCCT[C/G]TTCACTGTTGTACCT | 5521 |
rs188447624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692903 | ACATGCTTTGGTGGG[A/C]TTGCCTTATCAGATC | 5521 |
rs188450498 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665279 | CTGTTGTTTAGTGTA[C/G]CCACCGCCACCCATG | 5521 |
rs188452172 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070385 | TACTAAGAAAAAGGC[A/G]TAATCCTTACTTGAA | 5521 |
rs188455947 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658203 | ATACGGAAACCCTGA[C/T]CCTGGTGCTCTGGGA | 5521 |
rs188456292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054665 | AGGATTCTACCTGGA[A/G]GATGAAAACAAGAGT | 5521 |
rs188456302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707449 | ATGCCACTGGCCCCA[C/T]CATAGGCCACCCCGG | 5521 |
rs188456377 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649533 | TACTGCAACCTCTGC[C/T]TCCTCAGTTCAAGCG | 5521 |
rs188466815 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635352 | GTCATGGGTTTTTTT[G/T]TGTGTGTTTATTTCA | 5521 |
rs188468651 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629230 | CTCAATCTGGACACA[C/T]CCAAAAGAGAATGCT | 5521 |
rs188473442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696325 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 5521 |
rs188475698 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618267 | ACTGGTCACCGCTGT[C/G]TTTGAAGATGGAAAG | 5521 |
rs188483055 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662406 | TTAAGATTGACATTT[C/T]AGGGTTACATTGTCT | 5521 |
rs188484051 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063016 | GGGAAGAAGGGAAGG[A/G]GGAAGAGAGGAAGGA | 5521 |
rs188485074 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079991 | TTTAAATATAATTTT[A/C]TATGGATTTATTTAT | 5521 |
rs188485850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597694 | CCCTGAGCAACCCTA[C/T]CACCCTACAACATTT | 5521 |
rs188490632 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831745 | CAGTGAGCCGAGATT[G/T]TGCCAGCTTGGGTGA | 5521 |
rs188494794 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849262 | GTGCATATAACCCTA[A/T]GTATATCTACATAAA | 5521 |
rs188499608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633404 | TTGACTGCAGGCTGC[C/T]GTTTGAGGAGGATGG | 5521 |
rs188500754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826487 | GTGAATCTAACCCAA[A/G]ATAATCTTCAGTTTC | 5521 |
rs188516066 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041052 | CAGTCAAACCACTTT[G/T]CATGTAAGTACAGAG | 5521 |
rs188517901 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978772 | GTTTTGGTTACTGTA[G/T]CCTTGTAGTATAGTT | 5521 |
rs188520270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065203 | GATGGAGAACATTCA[A/G]GACCTTCTACAAGGG | 5521 |
rs188540474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918742 | TATATTCCCTTGTAA[C/G]CACATTTCTCCCACT | 5521 |
rs188550230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942755 | TCCTATGTGAAATTC[C/T]AAATCATGGCATTTC | 5521 |
rs188551144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043055 | GCAGAATACTATACA[A/G]TCTGGATTGTGGAAC | 5521 |
rs188558583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006127 | CCCTTCAGGATAGGA[C/T]GATGGATGGTTCCTC | 5521 |
rs188572541 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922402 | GGATGATATTCACTA[C/T]TGGACACATTTGATG | 5521 |
rs188584993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881663 | GTGATCTACCTGACT[A/G]GGCCTTCCAAAGTGC | 5521 |
rs188604307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913243 | TGTTATTATTATTGC[C/T]TCTTCAGGATGGTAG | 5521 |
rs188615022 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859153 | AACTAGGTATGTGAT[C/G]ATAGACAAGTTGATT | 5521 |
rs188616825 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835413 | GCATAGAGCCCACTT[C/T]AGCAGGTCAGTTGAC | 5521 |
rs188637518 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889601 | ATCCAACAATTGAAA[A/C/T]GTTGCAATTGGAACT | 5521 |
rs188652424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771369 | CAATAAATCCCTTGC[A/G]AACAGGTGCTACTAA | 5521 |
rs188658466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807990 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 5521 |
rs188661055 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808390 | TTTTAGAGAATCCAA[G/T]TGCTGAAAATCATCA | 5521 |
rs188662972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788836 | AAAACTCTCTGCCTT[A/G]GGGTTTTGACTCACA | 5521 |
rs188667919 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736477 | GCCCGGAGAGATAAC[C/T]AACTTGCTCCAGATC | 5521 |
rs188669106 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738156 | AATCCCAGCACTTTG[A/G]GAGGCTGAGGCGGGC | 5521 |
rs188669783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797858 | AGAAAGCGGCTGCCT[A/G]AAGACAGCTGGCTTA | 5521 |
rs188670433 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589653 | GAACAAAACACTGGA[C/T]CCACCAGAGAAAACT | 5521 |
rs188683882 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755492 | AGTCATATATAATAA[A/G]TGATCATTTTTACTC | 5521 |
rs188685660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722174 | TCAACTTTACTACCT[C/T]CAGATACTATTTACT | 5521 |
rs188686726 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891421 | TGAACACTGTCATTG[C/T]CTACATGGATGCTAG | 5521 |
rs188686965 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930587 | GAACAGGCTTCCCAG[C/G/T]TTAAGGTGGTAATCT | 5521 |
rs188689598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761541 | AGTGGGGGGTGCAGC[A/G]CACCAACATGGCACA | 5521 |
rs188695762 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703258 | TCACTTTTTGTCTTT[G/T]GTCAGGTACAAAGGC | 5521 |
rs188698319 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067829 | ATACTTGGATTAGGT[A/G]TAAGAAGTCCTAATT | 5521 |
rs188701512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668099 | ACCTGACTGCTGCAG[A/T]TAACAGAGCTCATCT | 5521 |
rs188702395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051499 | CATCTTCCTAGAAAG[A/G]CTTGACTCAAGCTGA | 5521 |
rs188704358 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704416 | ACATGGCTTTCACCT[G/T]TAAATTGTAAGTTTA | 5521 |
rs188708753 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875858 | GGTATACTAACACTT[C/T]TTAAGGAATTCATTG | 5521 |
rs188713712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685947 | TAAAACGTTCTGAGA[A/G]ACATCAATCAATAAT | 5521 |
rs188714850 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923771 | AAGACACATGCACAC[A/T]TATGTTTATTGCAGC | 5521 |
rs188716654 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056296 | AGTGCAATGAAATGG[G/T]TCTCTGTCCTTGCTT | 5521 |
rs188720291 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637508 | CTAACCTGTCTCCTT[G/T]TTTCTTTGTTCTCTC | 5521 |
rs188721381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962587 | GCTTGAACCCAGGAG[G/T]CAGAGGTTGCAGTGA | 5521 |
rs188723208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948104 | AATCGTTTCCCTTAC[C/T]CTATAAACCCTTAAC | 5521 |
rs188732068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676603 | AAGATCAAATTCTCC[A/C]CATCATCTGCTCTCC | 5521 |
rs188737469 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828633 | ATGGAGATAATACCA[A/G]AGAGTGACTGTATGG | 5521 |
rs188743786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844918 | TCCTAATCAAGAAGC[C/T]CCTTCCCCTAAAGCT | 5521 |
rs188746018 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645465 | TCATATTAAATATGT[A/G]TTGGGCAGGGTGAAA | 5521 |
rs188747957 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861212 | AGGTGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 5521 |
rs188756959 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608361 | GACATATTGGGGCTA[C/G]AACCTGGGCTTCATC | 5521 |
rs188757549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053202 | GATTCAAAACCTATG[A/G]CCTTCCTGCATTAAA | 5521 |
rs188760711 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608664 | GCTGGGCATAGTGGC[A/G]CATGCCTATAGTCCC | 5521 |
rs188761349 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596877 | GCTCCCAAACCTTTC[G/T]CCAGCCCTGCTGGAA | 5521 |
rs188761701 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018321 | TCATGACATAGCCAC[C/T]ATGAAAGGCAGTATT | 5521 |
rs188765356 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035985 | TTGTGTATAAAGTAC[A/G]GTGATTATTTTTTAA | 5521 |
rs188769604 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069845 | TCCCAGGCTGGAGTA[C/T]AGTGACACAATCTTG | 5521 |
rs188774787 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981830 | ATGTTATATAAATGG[A/T]ATTGAGAGATACAAT | 5521 |
rs188781123 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959015 | TTGTTTATTTCACAT[C/T]TGGTTCTTACATAGT | 5521 |
rs188796747 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916911 | TGATAAGTTACTTAA[C/T]ATCTTAATCATGAAT | 5521 |
rs188799461 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082229 | TTCCTATACGGAAAC[C/T]TTCATCTGCTTAGCC | 5521 |
rs188806678 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899377 | ACTATCGCAAGAACA[A/G]AAAACCAAACACCGC | 5521 |
rs188818583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883188 | ACCTTTGGTGAGTAG[C/T]TTAACATCTCTGAAC | 5521 |
rs188820782 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986764 | AACACTTATGAGCTA[C/T]ATAAGATAGTATCAA | 5521 |
rs188823919 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007965 | AATTCCGGACACAAT[A/T]GTCCATAAGGTTAAT | 5521 |
rs188826840 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963750 | ACACTGCTAACACCT[C/T]GCACAGCCTAAATTC | 5521 |
rs188827028 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001444 | CACTGCAAAGGTCTG[A/T]GGCTTCACTCCTGAA | 5521 |
rs188827566 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901492 | GGTGACAGAGTGAGA[A/C]CCTGCCTCAAACAAA | 5521 |
rs188828979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970141 | TGTAGGTATACTTAT[G/T]ATTCCCATTTTGCAG | 5521 |
rs188833255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949168 | GAGTGGTACTATTAA[A/G]CTTCAAGAATAGTTT | 5521 |
rs188836888 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931704 | GTGGGTGGTAGAAAG[A/G]ACTGAAATTGTCCAA | 5521 |
rs188842817 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591133 | CAAGTGCCATCACAC[A/G]GTGGTTCCCCTGGAG | 5521 |
rs188856708 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869336 | ACAAAAACACATATA[C/T]ACAGATAATCACTGC | 5521 |
rs188863982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894098 | TATCCATTTACGCTG[C/T]TACTAAGTTAGCCTG | 5521 |
rs188870695 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864243 | TACAGTGGTAATTTA[C/T]AAGATTTGTACTTTT | 5521 |
rs188871239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658923 | TGCTGTTTTGATGTA[A/T]TGTGTTCTATTAATA | 5521 |
rs188887975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897679 | ATATACTGGAGACAA[C/T]AGGGATACTTTTAGG | 5521 |
rs188892268 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838530 | GAGCTAAGATTGTGC[A/C]ACTGCACTCCTGCCC | 5521 |
rs188906776 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774087 | ATAAGCCTTGGACTA[A/G]TCCTAATCAAAATTA | 5521 |
rs188917134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810677 | TGTGTTTTCTCATTC[A/G]CTGACTTCCAGTCTC | 5521 |
rs188939834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778120 | TTTTTCCAGAGGCAA[C/T]GGAAAATGGCAATTT | 5521 |
rs188948925 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740457 | TGAAGGGCTCTTGGA[G/T]TCAGAGAACTCAAAG | 5521 |
rs188956324 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743184 | CTCTCTTAACAACAG[C/G]CTTTTGGTCTGAAGA | 5521 |
rs188962440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703786 | ATTCTGCATTATGGA[A/G]TATTAGGCATGGTCC | 5521 |
rs188963923 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720117 | GCAGCTGCTGGTCTT[C/T]ACTGTTGAGTGGTAT | 5521 |
rs188967493 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713889 | AAGTACAGATGTTGA[A/G]GAGATAACTGGAAAT | 5521 |
rs188971916 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684869 | GAGTCCAACTCAAAC[A/C/T]TTCTAAACCAGCATC | 5521 |
rs188986478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685282 | TTACTATTTGCAAGG[C/T]CTTAAGCCAGTACTT | 5521 |
rs188992356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669019 | AAGCTCTGAGGCTAA[C/T]AGAAAGGAAAGGAAA | 5521 |
rs188994710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651976 | GAGGAAACACAGAAT[C/T]CTAGACAGATGTGGT | 5521 |
rs188999657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056622 | AAAACTAAGTTGATA[C/T]AAGGATTACACAACT | 5521 |
rs189002164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010845 | ATCTGGCCACTCCCA[A/G]CCTACTCTACAGCTG | 5521 |
rs189003648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051128 | AAATAGACTGTTTCA[A/G]TGTAATCCAAAGGCT | 5521 |
rs189004569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828436 | TTCCTTATTTATAGA[C/T]AGCTTAATTGCATTA | 5521 |
rs189004747 | snp | A/T | 0.373598 | 0.21731 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844378 | AAAACATTAAAAAAA[A/T]ATATATACTGAAACA | 5521 |
rs189007853 | snp | A/G | 0.000205881 | 0.0101439 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638209 | CCCCAGCACATTGGG[A/G]CCAGTGGCCATGCCC | 5521 |
rs189011662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031545 | AGTTCAATGGTTTTC[A/C]TAAATTTTAGAAAAA | 5521 |
rs189011931 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621613 | TTAACCAGAGTGGAG[C/T]CATCTCTTTACAGAC | 5521 |
rs189019165 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032650 | ACTTAGAATATAGTC[C/T]CCATTCTCATCCAGA | 5521 |
rs189019870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067198 | GAACACTAAAAATCT[A/G]CTCAGCAATTTTCCA | 5521 |
rs189022241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601101 | AAGGTTCATCCATGT[C/T]GTAGCATGTATCAGG | 5521 |
rs189024558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800880 | TAAATGTCTGTCAAC[A/G]GATGAATGGATGAAG | 5521 |
rs189032683 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781257 | ACATCATAACAGTAG[C/T]GTGAGTATATCAACC | 5521 |
rs189046977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815036 | ACGTGACTCAGATAC[A/G]TTCCGCTGCTAACAC | 5521 |
rs189053151 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746843 | TGTGAGATAAAAGTG[C/T]TGTAGGGATATTTAA | 5521 |
rs189063988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944056 | CTACAGAGACCAGCC[G/T]CCTCATCCTTATCTC | 5521 |
rs189066804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998237 | TGAGAGTGAAGAGAA[A/G]TGAGGTAAACCTCAT | 5521 |
rs189069437 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763239 | ATGAAGGAGGAAATG[G/T]AAATAGCTCCAGGGC | 5521 |
rs189074977 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967402 | AATGATCTCATTTAA[A/T]CCTTATAACAGCCCT | 5521 |
rs189081286 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983587 | TTTTCCCAGTTCTAG[C/T]AAACTACAGAAATCT | 5521 |
rs189083033 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730953 | TTCCAAGAAGAAACC[A/G]ATGAGGCCTTCGAGG | 5521 |
rs189094242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996850 | CTCTCCTCACTCCAT[A/G]TCCCACCAGGCCTCA | 5521 |
rs189098439 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029593 | CCCCTGCAAATTTAT[A/G]TATTAAAACCCTAAC | 5521 |
rs189104369 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973852 | CAGTCACTGCATTAG[C/T]GAAGGAAACAATGCA | 5521 |
rs189108999 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820593 | TATAAAAAACGCCAT[A/G]CTGTTTGGGGATATT | 5521 |
rs189110533 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878402 | AGGGGTCTGGTCCCG[C/T]CCGCCCGCCCCGGAG | 5521 |
rs189113241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902552 | CAAAAATCCTGAGGT[C/T]TGGCTCTAGATATAC | 5521 |
rs189117070 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850280 | CGTGTCTCTTTAGAT[A/C]TATTCTAGACCCTTT | 5521 |
rs189131922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910563 | CCTCATCTGCAAAAG[A/G]GTGATGGTAATAGCA | 5521 |
rs189139561 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823144 | AGATTTCATCTGACA[G/T]CCTGCATATCACTAC | 5521 |
rs189155476 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759496 | GCAACAGAATTCTGA[C/T]TGTTCTGTCCCCACC | 5521 |
rs189156202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836439 | AGTCAGATTAAGAGA[C/T]GGCACTGTCCCAAAT | 5521 |
rs189156987 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824288 | TGGAGATTCATGACA[C/T]GGAAAGAATCACAGG | 5521 |
rs189157565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772330 | TAAAACTTATGAGCA[C/T]GTAGAATGTATATTT | 5521 |
rs189171591 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790114 | AGTTAATTGCCCTTC[G/T]GGACTGCTCTGTGTA | 5521 |
rs189196326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726453 | AACACACACACATAC[C/G]CTGATTATTAACAAT | 5521 |
rs189198827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594378 | GAATATTTTTCTCCA[A/G]CTACATTCAGCAACT | 5521 |
rs189207025 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689097 | CCCACTATCAGTAGG[C/G]GGTAATAATAGCCAT | 5521 |
rs189225921 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895030 | AAATGAGTAAATGAA[A/G]GCAAAACTAAAAGGA | 5521 |
rs189226835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757924 | AACTCTTCCATGCAC[C/T]TTGAAGGCTTGGTCG | 5521 |
rs189234383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037433 | ATGTACATATATGTA[C/T]ATGTATATATAGGTA | 5521 |
rs189245325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945044 | CAAACTGACTTCTAG[G/T]ATACGTTAGCCATAG | 5521 |
rs189247339 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864793 | GCTGTATCTTTAAGA[A/T]TTTTTTCTCTGATCT | 5521 |
rs189253690 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879000 | CGCCACTCAGCTAAG[A/G]GCCACGTCTACGCTA | 5521 |
rs189255994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592615 | TTTTGATCTGGAAAG[C/T]CTACTTGGCATTAAT | 5521 |
rs189262165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927188 | ATAGGCCTTTGGCTG[A/G]TTTCCAGAGCACAAA | 5521 |
rs189264874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602716 | TGAAGAGAATAGCAA[C/T]AAAAGCCCTGATCAA | 5521 |
rs189268423 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911244 | GCACACCACCATGTC[C/T]GGCTAATTTTTGTAT | 5521 |
rs189270146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070920 | GGCATCTGCTGTGAA[A/G]TGGAGATTGCAGTGG | 5521 |
rs189270178 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595825 | TTCTTTCTTCATGTT[C/T]CTAGTATGACTTTTC | 5521 |
rs189280306 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980477 | CAACCCACCCCAGAG[A/T]TTAAGATTAGGAACA | 5521 |
rs189286262 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948833 | AATAAGTAACTATAA[C/T]TGAGTGAATGTGCAA | 5521 |
rs189292110 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041518 | ACCCTGAACTAGACA[C/T]GGAAGGAGGGAGGAG | 5521 |
rs189297148 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983249 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAAGCT | 5521 |
rs189303972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012959 | ATACCTGTTTGCAGA[C/T]GACATGATTGTATAT | 5521 |
rs189328994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744863 | GGTCATTCACAGCCA[C/T]CCAGAACTTTCAAAT | 5521 |
rs189329770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919810 | AGAATAGCAACTTTA[C/T]AGGTGAAAAGCTCAG | 5521 |
rs189335731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903556 | GCATGCCACCACACC[C/T]GTCTAACTTTTAAAT | 5521 |
rs189349401 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730200 | TCTCTGGATTTCAGA[A/C/T]ACTTGCATAGGCTCA | 5521 |
rs189352446 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887352 | ATTTGCAAAAAGAGT[A/T]TTAATGTGTTCTTTA | 5521 |
rs189357084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952825 | TTAACCTTGGCTGCT[A/G]GGTATGTGAGAGTCA | 5521 |
rs189357229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966578 | GCAAAAGCATATCGT[C/T]GTCTGAAAACATTAC | 5521 |
rs189360327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915411 | CATCATCTTCCCCTC[C/T]TACTCAATAAATCCA | 5521 |
rs189360966 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865040 | TGTTCTAAAACATAA[A/C]CAAAGACATGATTTA | 5521 |
rs189361828 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693639 | TGAGTATATCCCATA[C/T]AGTTCAATCTTACAA | 5521 |
rs189368404 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712164 | TTACGATGGTTTTTC[A/C]AGGGTCTTAGCAAAT | 5521 |
rs189368646 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678119 | AACATGGTGGTTAAG[A/T]GAACATTGATGCAAA | 5521 |
rs189370154 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934438 | TGATGGCCAGTGATG[A/G]TAAGCATTTTTTCAT | 5521 |
rs189372870 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041824 | CAAAGCTTTGTTGAT[A/G]ACAGTGTAATGCCCA | 5521 |
rs189381510 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895357 | TACTTTCACCACAGT[A/G]TAGCTCTACATCTAT | 5521 |
rs189384725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077452 | GAACTGAAATAGAAA[A/G]AGCCATTAATAGGAA | 5521 |
rs189387090 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057683 | ACTACCAATGTTGCT[A/G]CTGTTAGCCTTCTCT | 5521 |
rs189388947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646489 | CTTATGTGGGAAACT[C/G]TTACACAAGACAAGG | 5521 |
rs189389305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919052 | TATGCAAAACCTATA[C/T]ATGAAAGTTCCCATT | 5521 |
rs189395091 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871497 | ATTCCATAAACATTT[G/T]TTTCTGTTCTTATTA | 5521 |
rs189399562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832566 | CCAGCTAGTTTTTTT[C/G]TATTTTTAGTAGAGA | 5521 |
rs189420252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804876 | TGAGGCTGGGCAGAA[A/G]CAAGGCAGCCTATGT | 5521 |
rs189420876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805622 | GAAGAAATTCATTGA[C/T]AGCAATGGAATATGG | 5521 |
rs189436615 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768132 | AGGTTGGAGTGCAGT[A/G]GCACACTCACAGCTC | 5521 |
rs189440728 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734268 | CCCTACATTGCCCAG[G/T]CTGGTCTTGAACTCC | 5521 |
rs189441335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003898 | CCCAACTCACTCGAG[G/T]GTCAATTGATTCTAA | 5521 |
rs189452466 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022536 | CTGCACTCCAGCCTG[G/T]TGACAGAGCAAGGCT | 5521 |
rs189453279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775211 | AACTATAAACTAACA[C/T]ATTTTATGAATACCG | 5521 |
rs189464335 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741603 | GGGCGACCGCCTCTC[A/G]GGACGTGGGGACAGA | 5521 |
rs189468383 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708214 | TAAAAAAAATTAGCT[C/T]GGCATGGTGGTGTAT | 5521 |
rs189483518 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674682 | CTCCATCATTGGCAG[C/G]AGGAATATCTGGGCT | 5521 |
rs189499658 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081784 | TCAGTTTCTGACAAA[C/T]GTGGCCTATTTTGTT | 5521 |
rs189501579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674995 | TAGAGATGGAGTCTC[A/G]CTCTGTTGCCAGGCT | 5521 |
rs189503905 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642406 | CATCATTTCCTAATC[C/T]CAAGTTTAGAAAAAG | 5521 |
rs189509502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019025 | TTTATTACTGCAAGA[C/T]CATAATTCACAAAGG | 5521 |
rs189522990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987253 | TATAATAAATACTAA[G/T]GTGGGATCTTCAATC | 5521 |
rs189523136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606521 | CCTATGTTCTAGGGC[A/G]GTTGTGAGAATAGAC | 5521 |
rs189528958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961075 | TTGTTGTTTAAAGAA[A/G]TATTACCTTAGTTGT | 5521 |
rs189529052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946451 | TTTCATTTTCAAAAG[A/G]CAGTGCAATCAATAG | 5521 |
rs189529065 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593324 | ACTAAATAAGTGGTA[C/G]ATTCTCATTTTCTAA | 5521 |
rs189536808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055046 | TCCCCAGAAAAAAAC[A/G]GGAAATGGGGAAGGT | 5521 |
rs189541131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956574 | GCTCCATCTCTTTCC[A/G]TAAGTCTCCCCATGC | 5521 |
rs189547222 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617729 | AAGCAGAGTCTCGCT[C/G/T]TGTCACCGAGGCTGG | 5521 |
rs189550895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991396 | TAGAAGTAGAGAGTA[C/G]AATAGTGATTACCAG | 5521 |
rs189554876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005416 | AAGAATAAATGTGTA[C/T]ACAGATAGCAAGTAT | 5521 |
rs189559622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962771 | CATCACCCTCAAGTT[C/T]GCTGCGGAACTTGCC | 5521 |
rs189565698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977845 | AAACATACACGTACA[C/T]GTGTCTTTATAGTAG | 5521 |
rs189566445 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804656 | GAGTCCCTTAGAAAG[C/T]TTAAACTGAAGTGAG | 5521 |
rs189570271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784400 | AAAATAGATGTGATG[A/G]AGAAATATATTGGCA | 5521 |
rs189571366 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018612 | TAAATGTTGATGTAA[C/T]GATGAGAAACCCAGC | 5521 |
rs189577007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742121 | AGAAAAAAATGTTTT[A/G]AAGAATTACTGGCTA | 5521 |
rs189577113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819297 | GTGGGCTACATGGAG[A/G]GTTCTCCTTTTGTCA | 5521 |
rs189590668 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751163 | TCGTGGCATGAGGTA[A/C]TCTTGAGAAGGTTAA | 5521 |
rs189593127 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726686 | TCTAGTCCTTGAGTC[A/C]ATATCTTAACAACAA | 5521 |
rs189600119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994843 | TGGTAGTCAAGACAG[A/G]CATAGTTCTTGCTCT | 5521 |
rs189607852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708747 | AGATTTTTTTTAATC[G/T]TTCTGTCTAGATGTT | 5521 |
rs189616032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675318 | AGTATTGCCCAAACA[A/C]CTTAAGCTTTTGAAT | 5521 |
rs189618294 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689561 | ACTCTATGATGTTTT[C/T]ACAACAATGAAGTCA | 5521 |
rs189620654 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656959 | TTGGGAAATACCAGA[A/T]CATCTTTAACTTCCC | 5521 |
rs189630311 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643775 | AGAAAAAGGCATATG[A/G]TATAATCCCAACTAT | 5521 |
rs189636583 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626351 | TTGTTATGATACTTA[C/T]ATGAATGTTAAAAGA | 5521 |
rs189636911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930897 | AGCTAAACATCCAGG[A/G]GAATGCTTAGCAAAT | 5521 |
rs189637615 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868139 | TTGCTGAGTCCCTGA[C/T]TCACTCCAGCCCAGG | 5521 |
rs189650854 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898501 | AAGACTTGAACATTA[C/G]ACCTAAAACCATAAA | 5521 |
rs189665201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781714 | CACCACATTTCACAG[A/G]ATCATAGTTGTCCCA | 5521 |
rs189671097 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835953 | GCTATGGGACCAATT[A/T]TGAAACTTTCCAAAG | 5521 |
rs189673175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815654 | GATTAGCTGGACAGA[C/T]CCTTTTACTGTTGGG | 5521 |
rs189679986 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784688 | CAATACAATTTCTTT[C/T]TGTGTGGCTCTCAGC | 5521 |
rs189693970 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819639 | TATGTTTTTTTGTAT[A/G]AATGTATATTAAAAT | 5521 |
rs189704330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904294 | GAAAGGTCAGTATTC[C/T]GGGGAAGAAAAAGGA | 5521 |
rs189706257 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676140 | AAACTGACAAAATGT[C/T]ATTTACTTCCTAAAT | 5521 |
rs189711620 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888391 | TGCTCTAACTTTGAA[A/C]TATGTCCAGAATCAA | 5521 |
rs189714703 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699486 | GAAAATGTGTCCCCC[A/G]TCATTCTACGAATGA | 5521 |
rs189716713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063812 | TTGAAAGGAACGCAG[A/C]ACATGAATCCAGGTG | 5521 |
rs189718867 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751637 | ACAAAGTCAACTCAG[C/T]TCTTACCCTCATGGA | 5521 |
rs189726925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644338 | AAAATTTCTTTTATT[A/T]CCCCCTGAACCCACA | 5521 |
rs189731230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872230 | AATGAATACTTGCTA[A/G]TGATTTTCAATGCAT | 5521 |
rs189733402 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717663 | TTGGGGAAGCTTTGG[A/G]GTAATACAACCTTTT | 5521 |
rs189733894 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683408 | CAAGTCCAAGCATTA[C/T]CACTTACTAGCCGTC | 5521 |
rs189737307 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081917 | ATGAATATATCAATA[C/T]ATATATTAAGAGATA | 5521 |
rs189739528 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628619 | GAGGGGCAGGTGAGG[A/G]AGAAGGAAGGTCTGC | 5521 |
rs189740420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920991 | TAAACCATTTCTGCC[C/T]GGGCAGACCAAATTA | 5521 |
rs189748297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607906 | AAAGCAGCATAGACA[A/G]TATGTAAACAGATGA | 5521 |
rs189749708 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826917 | TGCTATCTAACTTAT[A/G]TTAATTGGCTTTTCG | 5521 |
rs189751654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807203 | AAGATCTCTTCCAGA[G/T]TTTTCATTCTATAAT | 5521 |
rs189752728 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688552 | TGTTAGGTTACACAG[C/G]TGGTTAGTAAGAAAG | 5521 |
rs189764099 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841047 | GTAGGGATTCAGGAG[A/C]GGTAACAAAGTCAAG | 5521 |
rs189766305 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857745 | CAGGCTGGAGTGCAA[C/T]GGCACGATCTCGGCT | 5521 |
rs189768658 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653010 | TTGCCCTGAGAAACA[C/G]TACACCAAAATATTT | 5521 |
rs189775544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656072 | TAAATCCCTCCTCAA[C/T]AGCAGACATATTCTA | 5521 |
rs189791881 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624867 | CCCAGCTGGTCATCT[G/T]TCTGCCCTGTGACCT | 5521 |
rs189793011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146622156 | TCAACTTTAGACCTC[A/G]GTTCAAGCCCCCTCT | 5521 |
rs189794825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995294 | AATGTTGTATCCCCA[C/G]TACTTGCCCAGTTTC | 5521 |
rs189800660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047233 | AAGTTCCAGTGTTCT[A/G]TACCACTGTATGATG | 5521 |
rs189802392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617922 | CTGTCTCCAACTCCC[A/G]ACCTCAGGTGATCCA | 5521 |
rs189809065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028542 | TTCATTCTTGTAAGC[C/T]GTCCTTTGTATAAAT | 5521 |
rs189815898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970945 | TTGTGGTAACTATTT[A/G]TTGTATATCCCTTCA | 5521 |
rs189829153 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061549 | GGGTATGTTGTCTTT[C/T]TCGCTCATTGCATCC | 5521 |
rs189833597 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001691 | CATCGGACCCCTTTC[A/G]TTTGCTATTCTGTCC | 5521 |
rs189834904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026604 | TTACTGTAGGCCAAC[A/T]ATACCTCAACAAATT | 5521 |
rs189837641 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036774 | TACGCATTTGGAGGA[G/T]TAACCCTGCCCTTAA | 5521 |
rs189849334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939525 | TGTTTTGTAAGTCAT[G/T]CATAATTCTTCATAA | 5521 |
rs189857483 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914849 | GTGTGGTACAATTTA[A/G]GGCCAGGGTACTTAA | 5521 |
rs189878707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940299 | AGCGCCACATCTACT[C/T]GGCCAGGATAGTTGA | 5521 |
rs189892343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874823 | CTGGGGTTCCATATC[C/T]GAAAAAAAAAATCAA | 5521 |
rs189912153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882427 | CGACAGACTATAGTG[C/T]AATGTTAAGTGCCAA | 5521 |
rs189917221 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907050 | GCAAGAGGCTCCTTG[G/T]CTGATTGTGGTGAGG | 5521 |
rs189930882 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822737 | AATCTTGATCTTGCT[C/T]ACTTCTTTATGACCA | 5521 |
rs189941539 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853369 | TTAATCCATTATCCT[A/G]CTCATCTCTATATCA | 5521 |
rs189941557 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801817 | TATTATCATAATCCC[A/G]TTAATACATTTTATT | 5521 |
rs189952752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941562 | CATCTGTAGAAAAAC[C/T]AAAAAACATTAGGTT | 5521 |
rs189954484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900703 | GTAAATGTGTGTCAC[A/G]GTGATTTGCTGTGCC | 5521 |
rs189956625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146924024 | GGAGCTAAATGATGA[A/G]AACATATGGACACAT | 5521 |
rs189961291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763855 | AGCCTCCCAAGTAGG[C/T]GGGACTACAGGCATG | 5521 |
rs189968608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909060 | CCATGGAGAAGTAAT[A/G]GTGGGAGAAGATTTC | 5521 |
rs189973866 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870237 | GTTATGGACCAAATT[A/G]TGCCCCCCTCCACCC | 5521 |
rs189984102 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885272 | TAGATGAGAGCCTGG[A/C/T]GCCAACCCATGATCT | 5521 |
rs189996572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957010 | TATGAATTTTGGAAT[A/G]CATAAACATTCAGTC | 5521 |
rs190000878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824178 | ACATAATTTACTGAA[A/G]AGCAGAAAGCTTATT | 5521 |
rs190002793 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838302 | GAAGGAAGGGAGGCC[A/G]GGCTCACACCTGTAA | 5521 |
rs190007231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754817 | GAAGACTCCAGGCAA[A/C]AGCTGTGTTGGTGAG | 5521 |
rs190009552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695128 | CCTATTATTAAGTGT[C/T]ATATTAATAAAAACC | 5521 |
rs190016388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669888 | TTTTTTTCTGGTGAC[A/G]TTACTATATTTCCAG | 5521 |
rs190017273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854534 | TACCTTTTATCTAAC[C/T]GTATATTTGTACCCA | 5521 |
rs190021420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660219 | AAACCAAATAGAGTA[C/T]GTACAATGACTGTCA | 5521 |
rs190023437 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720844 | ACTTCACTCTCTTTC[C/T]AAATTTATCTGACTA | 5521 |
rs190024417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007185 | CCATCCGGAGGACAC[G/T]ACAACTGCAGGGCCC | 5521 |
rs190026424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045871 | TTGCAAATGTACTCT[C/T]CTTTGCCTAAAATAT | 5521 |
rs190031319 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027183 | CAGACAAAAAGGAAC[A/G]CATACAATACAAATC | 5521 |
rs190035464 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638730 | TGCAATCAGGCTAAA[A/G]TGTACCAAGTTGCAA | 5521 |
rs190042675 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630775 | TGGTAGGGAAGCAAG[A/C]CACCATCTTCACTCC | 5521 |
rs190045467 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635243 | AGCTGAGTTCTGATT[A/C]CAAAGCATCTGCTCT | 5521 |
rs190046178 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810356 | TGAAAGGAGTTTCCC[A/G]TTATAAAACCATCAG | 5521 |
rs190048773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796315 | ACAGAAGTCATCACA[A/G]AGGACAGAGTGAGCA | 5521 |
rs190051763 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006874 | ATAGTATGAGATGCC[A/G]CCCGGTGTTTACAGG | 5521 |
rs190057154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980716 | ATTGATTTACAGTAT[C/T]TTTTGCATGTAATTT | 5521 |
rs190061171 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924686 | CTGAAATTTGAAATA[A/C]TTTTTGAATAAGGGA | 5521 |
rs190063192 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589369 | TTCCTTGTCATTCTG[C/T]ATCCTCTTCTCAGCT | 5521 |
rs190066678 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812090 | GAGCTCTGAGTTAAC[G/T]TTGGACTTTTGTCAC | 5521 |
rs190066897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950484 | GCACAGTGAATCACC[A/T]GGAAAGACCTTGAAA | 5521 |
rs190068954 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909932 | TTTAGCAGTTTCATA[C/T]CTGATTGACATCCAT | 5521 |
rs190075309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893263 | TGATTCCTGAGCATT[A/G]ATGAATGCTTTCTTT | 5521 |
rs190083194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700664 | GGCAAATAAACTATG[C/T]TTTTTTCCTCCTGCA | 5521 |
rs190084996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776906 | AAAAGATGCTCAACA[G/T]TATTAATTATTAGGA | 5521 |
rs190085543 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995544 | AATAGTAATACTCTG[C/T]CAAAAAATGGAAAAG | 5521 |
rs190088116 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953556 | AAATACTTGTTATTT[A/C/G]AGTCACAAAAAGATA | 5521 |
rs190088953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742176 | AACTTTGCTGTGATA[A/C]TGCAGGAAATTGTTG | 5521 |
rs190090584 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045147 | TAGAGCCATTTACAA[C/T]TCTACATAATGTAAC | 5521 |
rs190092608 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760261 | CCCTATAAGGTATTG[C/T]TTTAATCTCTATTTT | 5521 |
rs190092837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719494 | AGAATAATATTGGTA[C/T]CATTTTGGAGGGGAA | 5521 |
rs190093916 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943169 | CATCCACACATGTTT[A/T]TAGTACAGGGTATGG | 5521 |
rs190097108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955460 | TAAATTGTTCTGTAA[C/T]GAAAACTATAAATTA | 5521 |
rs190098699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964125 | CCATTCCTAAGTATG[C/T]TCCCCAAAACATTTA | 5521 |
rs190103888 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727037 | AGAAGAGAGACACTC[C/T]AGTGTTTTGACACAC | 5521 |
rs190105278 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981162 | ATAGTACCTGGCACA[C/T]AGCAGGCACTCTACA | 5521 |
rs190105683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847166 | CTGGTCTTCTACCTC[C/T]ATCTCATTGTTTTCC | 5521 |
rs190108052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684120 | ACTGCAGTAGCTAAA[C/T]ACGCCATTGTTATAT | 5521 |
rs190108278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975718 | TGTGATTTTGATTTG[C/T]ATCTCCCTGATCATT | 5521 |
rs190110561 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920773 | TGCTGTGTGTGTGTG[C/T]GTTTGTTTTGTAGGG | 5521 |
rs190112271 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666922 | TGAATCTATTCTATA[C/G]TATTTGACTGTTTTG | 5521 |
rs190117237 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923279 | AGAGGTCTGAAGGAC[A/C]AGAGGGGACCACTTA | 5521 |
rs190121597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863201 | CTATTAAGTGACCAG[A/C]AGGTCTTGACTTCTA | 5521 |
rs190127973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877363 | GAATTCATAATGGTG[A/G]TTTTTAAAGGCCCCA | 5521 |
rs190129231 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003269 | CTCTAATCTCCCCCA[C/T]CCAGAAGGAAATAAG | 5521 |
rs190130517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636694 | TGGGTATAATATAAG[C/T]ACTCACTGAATGCAT | 5521 |
rs190135082 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620051 | TCTAGGGTAAGAATT[A/G]TCTCTATATTATGGC | 5521 |
rs190145263 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599721 | TGTTACATATGTATA[C/T]ATGTGCCATGGTGGT | 5521 |
rs190178860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887798 | ATCTGGACACTATTA[C/T]AACCAATGAAGGTGG | 5521 |
rs190180145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890633 | TGTAAGCAAGGTTGT[A/G]TATATTTTAAAACTC | 5521 |
rs190180843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857313 | GATATAAGAAGAAAT[A/G]TTCAAAATAAACGTG | 5521 |
rs190187724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860498 | GGTAGTATTCTCCTA[C/T]GTTTCTCTGACAAAA | 5521 |
rs190201271 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859776 | CAGCTCAACAACATG[C/G]GCTCTTTGGGTTTCT | 5521 |
rs190224116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800342 | TATTGTAAGGATCCC[C/T]GGGTACTGGTACCAG | 5521 |
rs190224703 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771022 | GCATTTTGAAAAGCC[A/G]CAGACAGCTTTCCTG | 5521 |
rs190238101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762953 | TCACTTTGAGTTCTC[C/T]AGTTGAGCCTCTGTC | 5521 |
rs190240799 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712941 | AAAGTACTATTCCAG[A/T]TATTAAAGAAAGATC | 5521 |
rs190242499 | snp | A/C/T | 0.0248432 | 0.108648 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738374 | GCACTCCAGCCTGGG[A/C/T]GACAAAGTGAGACTC | 5521 |
rs190244020 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680434 | TAGCATTGGGAGATA[C/T]ACCTAATGCTAGATG | 5521 |
rs190252783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704868 | GATTGTGAGGCTTAC[A/G]GAAACAGAGGAATCT | 5521 |
rs190254100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660950 | ACATTGTTATAAACT[A/G]TCACTGATGCTACAA | 5521 |
rs190261410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737198 | GAGAGCTTTAGCTGC[A/G]CTGTGAATGTTCATT | 5521 |
rs190272339 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678224 | TCATCCCTGGGATGC[A/C]AGGCTGGCTCAATAT | 5521 |
rs190272795 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647454 | GCTCAGTGCTTAGGG[C/T]GGTCTGGTTGAAAAG | 5521 |
rs190273272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023435 | CACCAATTAAAAAGC[A/G]TAGATTGACAGATTG | 5521 |
rs190275113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042224 | TTGTTTTAACTAGAC[A/C]CCCCCCTCCCCTTTC | 5521 |
rs190275814 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670557 | TTGCAGTGCAGTGGC[G/T]CAATGTCGGCTCACT | 5521 |
rs190276948 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632272 | AGGGAGAAGACAGCC[A/G]TCTACAAGCCAAGGA | 5521 |
rs190285030 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647278 | ACACTATGCTTTGGG[A/G]ATCCCAAATTATTCT | 5521 |
rs190285872 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615656 | TACAACAGCTACAAA[G/T]TAAAAACCAAGGATT | 5521 |
rs190288713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591309 | ATGTGTTTTTGGGCA[C/T]GTTGTCACCTGTACC | 5521 |
rs190299271 | snp | C/G/T | 0.0264882 | 0.11258 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609516 | GAATAGGAACAGCTC[C/G/T]GGTCTACAGCTCCCA | 5521 |
rs190304810 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791340 | CTCTTCAGTGTCGAT[C/G]CCCCCTTTTTCTATT | 5521 |
rs190315213 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810127 | ATTAGCCTTGTGAAA[A/G]TCAGGTATTGTTACT | 5521 |
rs190315680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823667 | AAAATCTTGGAAATG[A/G]ATTCAATCATCCATG | 5521 |
rs190321858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756925 | TGGTTCCTCTCCTTG[C/T]AACACTTACATTCTG | 5521 |
rs190326736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608973 | ACCGGACAAAGATAT[A/G]TCAAGAGAACTATAA | 5521 |
rs190334460 | snp | A/C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739423 | TCAGCCTGGCCAAAG[A/C/G]GCAAAGGATGGGGAG | 5521 |
rs190338264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773698 | AGGGTTTGAGAATTC[C/T]CTTTTTTTCTGCATG | 5521 |
rs190341577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960070 | CCTCTGTAGGGATGG[C/T]TGTGTTAGATAATAC | 5521 |
rs190347827 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010270 | GGCACCAGGGGCCGG[A/T]TTTGTGGAAGACAAT | 5521 |
rs190349071 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989212 | TACTTAAACTCTTCC[A/G]AAAAGCTAAAGTGAA | 5521 |
rs190352463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959258 | CCTTCTAGCATTAAT[A/G]TTTTCATTCAATTGT | 5521 |
rs190352727 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723968 | GTGCCAACATTTCCT[A/G]AGGACTGTAAGTTCC | 5521 |
rs190356367 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934509 | CTGTTCATGTCCTTC[A/G]CCCACTTTTTGATGG | 5521 |
rs190364445 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021453 | TAAGATGCACATGTG[A/C]AGTGTGAGACTCCAC | 5521 |
rs190375209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990415 | AAGCCCAGAAAGAAA[A/T]CCATGCACTTTTAAC | 5521 |
rs190379288 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050560 | GGTTCTAATCCTAGC[A/C]CTTGCATTTAACAGC | 5521 |
rs190384266 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862204 | GGGACCTGCAAGTCT[A/C]AACTCCCAAGAAAAG | 5521 |
rs190389509 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871918 | ATTCTCTCTGGGTTG[A/T]TGATGGAGATTAAAT | 5521 |
rs190399496 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816340 | AGGAGGCTGAGGCGG[C/T]AGTGAGCCATGATTG | 5521 |
rs190412230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928399 | GTTCCCACCTGGGGC[C/G]TCTTCCACCTATAGG | 5521 |
rs190413568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829547 | CTGTGATGGGGAGCA[C/T]TCTGCTGTCATGCTT | 5521 |
rs190418518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903774 | CAAATCCTAGTGATA[C/T]TGATAATTTTTTTGA | 5521 |
rs190420876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846646 | TCTTGCCACTGCACT[C/T]GAGCCTGGGCAACAG | 5521 |
rs190421815 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840888 | CACGTCCTTAATCTG[A/T]TAGAGCTTACTCTGT | 5521 |
rs190432446 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764905 | TCTTCCTAGTTATTG[C/T]CAAAATATTAAGCTA | 5521 |
rs190437522 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843753 | ATGGTTTCCAATTTC[A/T]TCCATGTCCCTACAA | 5521 |
rs190441048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802943 | GATAAATTTTACTCC[G/T]GTCCTCACTATCAAC | 5521 |
rs190442299 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840439 | ATAGTAGTTGCTTAA[C/T]AAATCTTAGTTTCTT | 5521 |
rs190449209 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782550 | CCAGTTATTAGCAAA[A/C/T]TTTTCTGTTTGCTCT | 5521 |
rs190455968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874285 | ATCACCTCTGCAAAA[C/T]GTCAGTATTTGTTGA | 5521 |
rs190463843 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748870 | GTATATAGGTTTTTG[G/T]GTGCACATACATTTT | 5521 |
rs190469834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756136 | ACTACTGAGTAGATT[C/T]AGTACTTCTGAAAGA | 5521 |
rs190473918 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019604 | TGTTTTGTTTTTTTT[A/T]AAAAAGTCTATCTAT | 5521 |
rs190475982 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982080 | ACTTCTAACCAGTTC[C/T]TACTTTCATTATTTT | 5521 |
rs190478188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987891 | CTCATGTCACTTATA[A/G]AGACATGCATAGACT | 5521 |
rs190480359 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814718 | GCACATGTGGTCCCC[C/G/T]CCAAGTGCTGGCAGG | 5521 |
rs190485981 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951360 | TGCCTTTTTTTTTTA[A/T]AAATTAAGTTCCAGT | 5521 |
rs190488036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964914 | TATTTGGGTGACTGT[A/G]AACAAGTCACTCCTC | 5521 |
rs190488270 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002565 | ATCCGATTTTTCTCG[G/T]TCTTCTTTGTGGTCT | 5521 |
rs190502996 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780298 | ATTTTATACATTAAA[A/T]TATTTTTTAAAATGG | 5521 |
rs190506720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776032 | GAAGACTTAATACTG[G/T]TAAGATGATAATGCT | 5521 |
rs190509226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723190 | ATTCCCAGTGTATGG[A/G]TATGGTACATAATAA | 5521 |
rs190513234 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686283 | GGGGTGAAGAGGAGG[A/C]AGACAGCGAAGAAAA | 5521 |
rs190539872 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717084 | CACATGACAGCTCTC[C/T]GCTTAGCTTAAAGTC | 5521 |
rs190545146 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066731 | GGACTGCTAGAAAGC[C/T]ATTTCTAATCATGAT | 5521 |
rs190553857 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682462 | AACCTCTGTAAGAAA[G/T]TATAGTTATTATTCT | 5521 |
rs190569213 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630521 | CATCACTTGCTCTTT[G/T]GTGGCCATAAGTGTA | 5521 |
rs190575245 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649497 | TCACCCAGACTGGAG[G/T]GCAGTGGTACGATCT | 5521 |
rs190586414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997703 | AGTAGACTCAGTAAT[A/G]TAATGTGGTAAAATT | 5521 |
rs190594225 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976822 | ATATTCATTCTTCCT[G/T]AAAATTTTACTATGA | 5521 |
rs190604092 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912552 | AGAGTCTCCCTCTGT[C/T]GCCCAGGCTGGAGTG | 5521 |
rs190609219 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967522 | GATTCTAAACCAGAG[C/G/T]GCTGGTTTGAACCTA | 5521 |
rs190609600 | snp | C/G/T | 0.00597694 | 0.0544006 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945860 | GAATGAGCTGAGACA[C/G/T]GTGTCAGATCTTTCT | 5521 |
rs190612042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897133 | AACGATGCATTTCAT[A/G]TGTTTCTGAGAGAAG | 5521 |
rs190612814 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723896 | CAACAAATCCACAAA[A/T]CTCATTAATCCCTTT | 5521 |
rs190622021 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960667 | ACCAAGCAATGTAGT[A/C]AAAAACCTAACCAAA | 5521 |
rs190625395 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998966 | TTGCAGTGAGCAGAG[A/C]TCAAGCCACTGCACT | 5521 |
rs190627574 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705681 | TTACTTTACCAAAGT[A/G]ACTTACCAAGTTTTG | 5521 |
rs190638368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946064 | TGAGCCAAGCCAGCC[A/G]TTAGTCATGTGGATT | 5521 |
rs190639265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881161 | CTAAAATGTCAAGTT[A/C]TTTCCAAAAGTGGTG | 5521 |
rs190639946 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052131 | GGCTTCTGTTTGTAT[A/C/T]TTCTTATTTCAAGTT | 5521 |
rs190642129 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671495 | CTGGTAAAGGGTAGG[A/T]TTGTCTTTTACATTT | 5521 |
rs190642622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928792 | AAAACATTCTGGTGG[C/T]TTCCCATTTTGCTTA | 5521 |
rs190644252 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686953 | AAGTAAAACTGCATA[C/G]GGACCTCAAGGCCTT | 5521 |
rs190648001 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033394 | TTCTCCCATTAGAAC[A/G]TAAGTTGCATTGGAA | 5521 |
rs190652069 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068352 | AGTGACACAGAAAGT[C/T]GTTTCATTGGGATTC | 5521 |
rs190657166 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851299 | CAAATATTTACTGAG[A/C]ATATTTACTAGATTC | 5521 |
rs190658536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653506 | CCTGGTTCCTCTGCC[A/G]TCAAGAGGTACCAGA | 5521 |
rs190662495 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640256 | CTGAGCTAACAGTAC[A/C]TGTTACTACAATTTC | 5521 |
rs190663941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913089 | GCTGTCCTCTGGAGG[C/T]CCTGTCTGCCCATGC | 5521 |
rs190665241 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866115 | GCTGGGACAAAGGCT[G/T]TATGGTCAGCAAAGG | 5521 |
rs190665910 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935303 | GCTAGAAGGCACTGT[C/G]TATGAGCCAGAACAC | 5521 |
rs190667857 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851943 | TGATAATCATTAAAA[C/T]CCTTGAGGTCTAGGA | 5521 |
rs190671532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146880967 | CACCCAAAACCAAGG[A/G]GAAAAAAGCTGTTGG | 5521 |
rs190677004 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623372 | AATTGAAAATGAACT[G/T]TATATTAGAAACATT | 5521 |
rs190695644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856779 | CCTTGCCTCAGCCCC[A/G]TCGACCTGAAGTGGA | 5521 |
rs190697327 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781919 | TGCAATCCGTAAAGT[G/T]GGAGGTGGGGCCTGG | 5521 |
rs190706023 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821986 | ACACACAGTGAATCC[A/G]TGGCCCAAGTAAGAC | 5521 |
rs190707274 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764267 | AAGCCTTGTGGGCCC[A/C]CTTTTGAAGGAATTT | 5521 |
rs190710063 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797305 | GCCACTATTGCTAAT[G/T]TTTTCATTTCCACAA | 5521 |
rs190715249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015227 | AGACCCTCCTTTCCC[C/T]AATTTTATAGACCAC | 5521 |
rs190717957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796057 | GCATCTCTGTTTCAC[C/T]TCTTCCACTGTAGGC | 5521 |
rs190726284 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985456 | ATCTGTGTTTTTGGG[G/T]TCAAATTCAAAAAAT | 5521 |
rs190734656 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826050 | TAGAAGCTGTAAAAT[C/T]TATATCCGGTAAATA | 5521 |
rs190738811 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759892 | GTTGTTGTTAGTAGT[C/T]ATTGTGATGTCTTAC | 5521 |
rs190742064 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748175 | ACCTGAGGCCCCAAG[A/G]GGCTGCCCATGGTCA | 5521 |
rs190742279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732081 | TATGACTCAGGCCTC[C/T]TGGAAAAGTCCTTGA | 5521 |
rs190746707 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696073 | CTGATTTTTTCCCAT[C/T]CCCCCGCCAACAAAG | 5521 |
rs190749791 | snp | C/G | 0.046775 | 0.145601 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761145 | GAAATACCATTTGAC[C/G]CAGCCATCCCATTAC | 5521 |
rs190752903 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059526 | ATGGCAGAGGTTTCT[G/T]GAGGGAGAGCTCAAG | 5521 |
rs190754897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713676 | ATTTTCTGGATGATA[C/T]TGAAAGTTGACCTGT | 5521 |
rs190765366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079858 | CTCACCACAAATAAA[C/T]GATAAATATATGAGG | 5521 |
rs190769138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680696 | GAGACAGTGTGTGTA[C/T]GCATGTGTGTACCAC | 5521 |
rs190773658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733911 | AGTAATAGTAGACAA[C/T]AATAACGGCAGTAGT | 5521 |
rs190775280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662324 | TCCATAGAATGTCAG[C/T]TCTGCCTCCCACCAA | 5521 |
rs190780491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691819 | ATTAAGCTCACTAAG[C/T]CTCGGGGCCTTTGCA | 5521 |
rs190786260 | snp | G/T | | | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081402 | GAGCAATTGGAGTTT[G/T]TCCCTTCTCAGGCCC | 5521 |
rs190800447 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665498 | CTCTAGGTTAGACTT[C/T]GGCTTAAGGAAATGT | 5521 |
rs190808141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075664 | CCCAGTGTTAGTAAC[A/G]GTGTCCACCAACCAC | 5521 |
rs190809827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697620 | CTATTCAATATGCCA[A/G]CCTCACAGAGACAGC | 5521 |
rs190819094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023820 | GCATCTTCCAATCCA[C/T]TGAGGGCCCAGACAG | 5521 |
rs190821701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664187 | GTTTGCCATATCGAT[C/T]GACTCTTCCTTTCAT | 5521 |
rs190822562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635605 | GGCCTCCACCCTGGG[C/T]TGGTGGCCCAGAAAG | 5521 |
rs190830209 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607379 | TAGATCGTATTAAGA[C/T]TCAGATGAAGGATTC | 5521 |
rs190833860 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042788 | GTGTGCTTTTCAGAC[A/G]AAGTAGGCAGGAAGG | 5521 |
rs190834018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981787 | CTACTAATCTGTTCT[C/T]CAATCCTATAATTTT | 5521 |
rs190838171 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598459 | TATGGCTTTAAATAC[C/G]CTCTACATACTTGTG | 5521 |
rs190838478 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984426 | ACTTTTCTTCTTTTT[A/C]TAGACTAAATAGTAT | 5521 |
rs190857255 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929131 | CCATCTGTGTGTCCC[C/T]ACTGCCCGCCTACCT | 5521 |
rs190874799 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007879 | CATCTTTAAGAACTG[A/T]AACACTCACTGTGAG | 5521 |
rs190905613 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950861 | TAGGTATGCCATTTA[C/T]CAGGTAATTAACAGA | 5521 |
rs190915326 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834279 | TTATTTCTCATGTTT[C/T]ATGTAGAGGAGAACA | 5521 |
rs190915387 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953967 | AAAGAACTGAAGTCT[C/T]CAGTATTTCTAAATT | 5521 |
rs190921067 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850986 | ATAATAAATTTGATT[A/G/T]GTCACCCCAAGGATG | 5521 |
rs190921589 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897320 | GCCCCCCGTTCCCAC[A/T]GTTTAACTCTTCTCA | 5521 |
rs190923905 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917791 | GTGAGCAGTCTAATG[A/C]ACTTAGAAATGATAC | 5521 |
rs190926811 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865607 | TACCTAGGTTTTTTA[A/G]CACAGTGCCTAATAT | 5521 |
rs190937400 | snp | C/G | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861539 | ACTCAGGTGAATATT[C/G]GCTACATTAATTCCC | 5521 |
rs190941582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820977 | GGCCATACCATCTCT[C/T]ACCAAGATTAGTGCA | 5521 |
rs190947305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639733 | ACTTTTTACTTAACA[C/T]TTTTCTTTCAGATCA | 5521 |
rs190947572 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806047 | CTGGGAGGCTTGCAG[A/G]TAACATTTTACTCAT | 5521 |
rs190950185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623041 | CATTCAATAACTACA[A/G]TTTAGTATCCATGAA | 5521 |
rs190950895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999426 | TATTACAATCCACTT[G/T]GGAGTTAAAAAACAA | 5521 |
rs190956449 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833009 | TTGCAAACTAGATAG[G/T]GAAGGTATTTCATTC | 5521 |
rs190958036 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829277 | AAAAAAACCTATTTT[C/T]TAATCTGTGACTCAT | 5521 |
rs190959096 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602979 | AATTCCAAGTAAAAC[A/C]CCTGATCCAGAGGCA | 5521 |
rs190963835 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773837 | GTTTTTTGTTTAATG[C/T]GAATTATTTATATAA | 5521 |
rs190968015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743786 | CTGTTACACCAAGTC[A/G]TAAGCTAAAATGTGC | 5521 |
rs190969278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768668 | AGGTCCCATACCATC[C/T]GACGCTGGGCCCACA | 5521 |
rs190969501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777516 | CAGTTTCTGTTTGGG[A/G]TAATGAGTATTTTTG | 5521 |
rs190978132 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761554 | GCACACCAACATGGC[A/G]CATGTATACATATGT | 5521 |
rs190987397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936265 | CTGCTGTAAGCAGTG[A/G]AGTCATTTGATACAA | 5521 |
rs190988024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786103 | GTTACCCTGATATGA[C/T]GATTACACATTGTAT | 5521 |
rs190991691 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692377 | ACCTGGCATTCTCTA[C/T]AGCATTAAAACAGAG | 5521 |
rs190999434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711044 | TCCCTTTATTATGCA[A/G]CCTCATTGCTCCCCA | 5521 |
rs191002209 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742686 | GCCCTCCCAAAATTT[A/T]TATGAAGTTTTAACC | 5521 |
rs191002506 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922273 | CTTCCAAGTGTGCAT[A/G]ATATCAAGGATTATT | 5521 |
rs191003465 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769816 | ATAAAAACAGGTAAA[C/T]ACACAATTATTTTAT | 5521 |
rs191008372 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709958 | AATGCATGTTGAGTT[A/G]GAAACTCCCTTGCCT | 5521 |
rs191009132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906047 | ATTTGGACATTTGAA[C/T]CTATTTTTTCAGCTG | 5521 |
rs191015371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735987 | TCCCCACCCAAATCT[C/T]ATCTTGAATTGTAGT | 5521 |
rs191025011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985112 | TGCAACCTATGCCTC[C/G]CAGGTTCAAGCAATT | 5521 |
rs191030869 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968344 | GACAAATCTTGTCTT[C/G]AATATACATTTGCTA | 5521 |
rs191032968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954547 | GTAAAAGACTACAAA[A/C]TGGGTGCAGTATTCA | 5521 |
rs191034195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709598 | AGTAAGTGAGGGAAG[G/T]CCTTCTGACCGGACT | 5521 |
rs191041704 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055893 | CCCGAGGAATAACTG[C/G]AGATGGGTCCCATTT | 5521 |
rs191063345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649652 | TTGGGGCCTTGCCAC[A/G]TTGGCTAAGCTGGTC | 5521 |
rs191065857 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675930 | CTTCCTCCTGCCCCA[A/G]GACTAATCGGAAGCT | 5521 |
rs191066469 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889027 | AATTTCCAGGGAGAG[A/G]GAAACGATTTTGTTC | 5521 |
rs191075194 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644009 | GTGTTCCAACAAAAC[G/T]TTACTTACAAAAACA | 5521 |
rs191080866 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618754 | CCACTCTTTCCTCCC[A/G]GCATTCCTGATGCTG | 5521 |
rs191090897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922933 | AGAACAATAAAGATC[C/T]GGAAGATAGTGGAAA | 5521 |
rs191090986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996539 | CTCCTGAAGATCCCT[A/C]AATAGGAGTATGGTT | 5521 |
rs191093141 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964408 | TGCTAAATAGTTTGA[C/G]TTGGTGCTTCGCAGA | 5521 |
rs191095627 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, splice-acceptor-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607693 | CCTTTTCTTTTCCCA[C/G]ACAGGAAAAACAGAC | 5521 |
rs191100802 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906354 | GGAGACAGAGTTTCA[C/G]TCTTGTTGCCCAGGC | 5521 |
rs191103935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988236 | AATCAACAAAGAAAT[A/T]TTGGAATTAAACGAC | 5521 |
rs191108905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889794 | AATTGTTGTCAGAAG[C/T]TAGGGCAGTTTTCGG | 5521 |
rs191118532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019860 | AGATCTGATTCTTCT[C/G]TATGAGAGCTATGGG | 5521 |
rs191125089 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055483 | CTTCAGAAAACACTT[C/T]CCTTTCCTTGTACAA | 5521 |
rs191135794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938305 | GAAAATGCATGGTGA[C/T]GATATTAACTCCCAC | 5521 |
rs191139918 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843128 | GGAGGCGGAGGTTGC[A/G]GTGAGCCCAGATCGT | 5521 |
rs191144733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859647 | CAAGAGCCAGTAAGC[C/G]TGGCAAACCCCCCAG | 5521 |
rs191145717 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932204 | GATTCTTGAATTCAA[A/G]GCCTATTGTATTTAA | 5521 |
rs191151147 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874209 | TTGTCTCATACTATC[A/T]CCTTTGCTAGATTGA | 5521 |
rs191160922 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932890 | AGAAGACTTCCTTGA[A/G]CAAGGGGGCAGAGGA | 5521 |
rs191166297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957935 | ATTACAGCCTATGGT[A/G]TTGGCTGCATGTCAA | 5521 |
rs191170680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828235 | GAATTTTCTATTATA[C/T]CCTAAAATATTACTT | 5521 |
rs191187728 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876526 | AGAGTTAGTCATGTG[C/G]TATCAGGTCACTGAG | 5521 |
rs191192912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037715 | AGGGATGAGTCAGAC[C/T]GGGAGCAGCATTTCC | 5521 |
rs191194911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635934 | CACGTCCATGTATGA[C/T]GAATGCCAACCTTTA | 5521 |
rs191200892 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071406 | AGTGGCTCTCTATTT[C/T]ATTCAGGCAGGAGTC | 5521 |
rs191201473 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793918 | TGGTCCCCACACTTA[G/T]TCAAATTCACTAGAT | 5521 |
rs191202778 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619263 | TGAGGTCAGCAGTTC[A/G]AAGCCAGCCTGGCCA | 5521 |
rs191203907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055365 | TGGTTCCAATGACTT[C/G]TTTGCATGTTAAATG | 5521 |
rs191208219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599078 | ATAGGGTTAGTTTAT[C/T]TCCAGCACTTGATCT | 5521 |
rs191211237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815905 | CCAATTGCTCCTAGT[C/T]GTGCCCTTTGAGGGT | 5521 |
rs191212194 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837884 | GATGAAGGTAGAGAA[G/T]AATGGTATCAGAGAA | 5521 |
rs191225944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846226 | TCTACAAGAAATACA[A/G]AAATTAGCTGGGCAT | 5521 |
rs191232938 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869913 | TTTCACTGAGTTTCC[A/T]GTGTGGCTCTCCCAC | 5521 |
rs191235559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753130 | AGAACCTGGATAAGA[C/T]GAGCAGCTGCTCCAT | 5521 |
rs191245779 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786458 | ATAAGGAAGACAGAT[G/T]CTGCCACTTCCTGAA | 5521 |
rs191281864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073459 | CTGGCAGATTGGAGC[A/G]CCATGCAAAGTGAAG | 5521 |
rs191288523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690431 | CAACACTTTCTCAAT[A/G]CATTTATCTTACTAT | 5521 |
rs191299356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687154 | CCTCACCTGGAATAA[C/T]AATGGCACTAATTAT | 5521 |
rs191299412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020220 | CTCTTGGTATTTGAT[C/T]CTGGAGAATCAAAAC | 5521 |
rs191301826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039561 | CCTGAGAAATACTTA[C/T]CAGTAAGCACCCAAA | 5521 |
rs191309287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747853 | TAGTAAACAGAACAG[C/T]TGTGAATTTTTTTTT | 5521 |
rs191317492 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713176 | TTGAAGGAGTGGAGG[C/T]GTTCACGATGCAGGT | 5521 |
rs191317928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657549 | GCATCCACATTCTCC[G/T]TCCTAAAATCAGATC | 5521 |
rs191323558 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654191 | GCCCCACCCAACTCC[A/C]AGGTGTTATCTCCTC | 5521 |
rs191328107 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627843 | CCTTTGGAGGACAAT[A/G]AAATTTCTGATTTGC | 5521 |
rs191330162 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002721 | CAACTCTTCTGATCA[C/G]CAGGGTCCAGGGACC | 5521 |
rs191331046 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958851 | AACCAATTTAAACCT[C/T]ACAACAAACTTATGC | 5521 |
rs191335486 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787562 | TCTCCCCTCTCCCTT[C/T]TCTCTTGTCTTCTCT | 5521 |
rs191339020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919211 | TGTCTTCTCAAAATT[C/T]CCTCCAGCTATCACA | 5521 |
rs191340142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623798 | TGATAATGATGGAAG[A/G]CCAGCAGGTGCTTTG | 5521 |
rs191343278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903245 | AATTTAACTGTCAAT[A/G]GACATTAACCACATT | 5521 |
rs191349100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925067 | ATTCCCTCTTCCCTC[C/T]TTTGTGCTATTACTG | 5521 |
rs191350836 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038028 | GCCCTCCTGGGTCAC[A/G]GAGAAGCTGGCACTC | 5521 |
rs191355960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754107 | ACCAAAGTTCTGCCA[C/G]AAGCCCCCGCCACGT | 5521 |
rs191359731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988933 | ACATTATAACTGATG[C/T]CACAGAAATACAAAG | 5521 |
rs191362171 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002742 | TCCAGGGACCATTGC[A/G]GGTTCTCGGGCAAGA | 5521 |
rs191367087 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736381 | CCACATATTTTACAT[A/G]CATTTGCTCCTTCAG | 5521 |
rs191367451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058417 | AATAGTAGGCACTCA[A/G]TAATTACTTCCTGAG | 5521 |
rs191370280 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973343 | CAAAACAACATAAAC[C/T]CTCATATTTTACATT | 5521 |
rs191373356 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769982 | ATCAAAACGATGTTT[G/T]TCAGCATTATTTATA | 5521 |
rs191381619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677357 | AGAAAGAACTCAGGC[A/G]GTTTCTAAATACACA | 5521 |
rs191383975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719647 | ATAAGGCAGAGCAAG[C/G]CTCCACAGCTCCACA | 5521 |
rs191387194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856022 | ATACCTTTTATTCTT[C/T]GTTATATTCAAAGTA | 5521 |
rs191387842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693372 | GTCACATGCCACCAC[A/G]CCCAGAGAATTTTTC | 5521 |
rs191389842 | snp | A/G | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082806 | CCATTTGACAGTTTG[A/G]GCCCTTTAGCCCAGT | 5521 |
rs191393615 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972096 | TCTGACAGTCTCTCC[A/G]TCTTCCTTTGCTCTT | 5521 |
rs191399150 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871354 | AGTGGGTGCCTAGAT[A/G]GCCCAGCGGGACCAT | 5521 |
rs191401470 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942496 | TCTTTCTTCTTTCAC[A/T]TTTTAGTTGCACTTG | 5521 |
rs191402352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659055 | TCAAAAACCTTTTAA[C/T]ATGATTTAGGGGAAA | 5521 |
rs191402379 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701371 | AACATCTGGAGAGAA[G/T]AAAAGGGAAAAACAC | 5521 |
rs191404714 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972576 | AATTAGCTGGGCATG[G/T]TGGTGGGTGCCTGTA | 5521 |
rs191407437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646146 | CATTACTCTGAAAGC[A/G]GCAAATTTGTTTTTT | 5521 |
rs191413490 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630062 | TCAAGCAACCCACCT[A/G]CCTCAGCCTCCCAAA | 5521 |
rs191422212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608824 | AGTGCCTGGTACACT[A/G]TCAGAAGTCACCAAG | 5521 |
rs191426680 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840081 | AGAGAGCTAAAATGA[A/G]AAGTTAATTATGTTG | 5521 |
rs191429238 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884155 | CCTACCAGTAGAAAC[A/C]CATTACTTGCTGATG | 5521 |
rs191446905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917449 | CAGCATTATATATGA[C/G]CCTCAGAGCCAAAAA | 5521 |
rs191459608 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854345 | TGATATTTTATTACA[C/T]GCATAGAATGTATAA | 5521 |
rs191465304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066206 | CTTCAAATCTCAATT[C/T]CCTCTGCCAAAATCT | 5521 |
rs191470785 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909469 | CAGTAAAGCTCTTCA[C/T]TTCAAAACCTGATTT | 5521 |
rs191474863 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876962 | GAAATGTTAGCATCC[A/G]AGAATAATAATTTTA | 5521 |
rs191480566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703954 | ACCTTTATTTTAATT[C/T]TACTAGCCAGCTGCT | 5521 |
rs191486513 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744231 | CCACCCTTTTAAATA[A/G]AAGAGGTTATTTGTG | 5521 |
rs191493477 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854161 | CTTCATTCCCAATCT[A/G]CTGACACACATTAAA | 5521 |
rs191498092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669424 | AGGTTTAAGGAAGTA[C/T]ATTTTTCACAAATGG | 5521 |
rs191501212 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685344 | AAATGGGCAGGATGC[C/T]TAAGTCACAGAATGA | 5521 |
rs191518378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823479 | TGGGATTACAGGCGT[A/G]AGCCACTGCACCTGG | 5521 |
rs191530943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732499 | AATCAGGAACAAAGG[G/T]CAATCTTGCAGAGGT | 5521 |
rs191534963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756550 | AGGAAAGTTAAAAGG[C/T]AGCCTCTGGGATGCC | 5521 |
rs191538524 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731642 | GAGAGTCAGTCACCC[G/T]CATTCTCAATTTCCT | 5521 |
rs191541693 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590305 | TACCATGTTATGGCC[A/C]GCTTATGACACCATA | 5521 |
rs191545571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790636 | GTCTTCACCTCTGAG[C/T]ACACCTGCACTGAGC | 5521 |
rs191548447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672449 | TTTCCTAGAGAAAGG[A/G]GTAGAGTCTGGAATT | 5521 |
rs191566564 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696535 | ATCAGAAGTCTCTTT[C/T]ATTCCAAGTAGTGTT | 5521 |
rs191568822 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640437 | CCCTCAGGAGGAGGC[G/T]CTAGGCTGCAGCTCC | 5521 |
rs191568946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146695419 | TTATGTCATAAATAA[C/T]TTGAGAGTCTAGATT | 5521 |
rs191574227 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804393 | TAGCATCTGGCAGAC[C/G]CGGGACTGGAACCCA | 5521 |
rs191576136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662444 | AACCTTGGCTGCACA[G/T]CAGAATCAAATAAGA | 5521 |
rs191589744 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603883 | ATTTTGAACTCACAT[C/T]TATCTGACTTCAAAA | 5521 |
rs191590424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078245 | TACTTACAAAGTATT[A/G]AGCACTGACGCCAAT | 5521 |
rs191599672 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078661 | ATTAAAAAAAAATAA[A/G]CTGGGCATATTTGGT | 5521 |
rs191600076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750749 | ATTGCTATGGCTTAT[A/G]TATTTTCAACATAAG | 5521 |
rs191608762 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784136 | TGAATAATAACATTG[A/G]ATGTTTCAGCCTATT | 5521 |
rs191611836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766219 | CTTAGTAGTCTTTGA[C/T]GTATTTTGCTGATGA | 5521 |
rs191628582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603514 | AATTCTTCAATCAAC[C/T]TACCACCATTTATTT | 5521 |
rs191642299 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004505 | GGTCCATTACCATCC[A/G]AGGAATCCTGGGACA | 5521 |
rs191646589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957325 | CCATGTAGTCTTGCT[A/T]CAGAAGCTCATAGTT | 5521 |
rs191651513 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954799 | GTGTGTTGAGTTGAG[C/G]GTATAGTGGCAATGA | 5521 |
rs191655569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977097 | CTTCATTCTTTCATA[C/T]CCGATGTCTAACACA | 5521 |
rs191656453 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049008 | GGTAAAAATAAGGGC[C/T]GTGAAGGAAAAATAA | 5521 |
rs191663094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042061 | TGGCGAGCTATATCC[A/G]CAGTTCCCAGGAATT | 5521 |
rs191668610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065519 | TGCTACTCTGGATAC[A/G]GTGTGAAGAATAGAC | 5521 |
rs191679040 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082415 | GAGACAGTTTCCTCA[C/T]CTTAAATGGCAATAA | 5521 |
rs191687134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824969 | CTCAAGTGATCCACC[C/T]GCCTTAGCCTCCCCA | 5521 |
rs191689868 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811040 | GAGTCTTGCCCTGTC[A/G]CCACCCAGGCTGGAG | 5521 |
rs191692179 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945270 | GTTCCTTCCTCAAAA[C/T]TTAAGTCCACTTTTC | 5521 |
rs191694060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965619 | ATCAGCAGAAGTGTC[A/G]CTGGCCCCGCTTGCT | 5521 |
rs191701059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982882 | TCAGTGTTTGTATAT[A/C]TTTTTCCATCCTTTT | 5521 |
rs191701138 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927765 | TTTAGATGGAGTCTC[A/T]CTCTGTCACCCAGGC | 5521 |
rs191702052 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839183 | GGCAAACATTACTTA[C/T]GCAATACTCAAGTCA | 5521 |
rs191705871 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775164 | CAGCATTACTTTGAT[A/G]CTAAAGTCAGACAGA | 5521 |
rs191716803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008958 | TCCTTAGATTGCACC[A/G]TTTGGGCCTCTTTAC | 5521 |
rs191719013 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759346 | ACCTCACCTTTTATC[G/T]GAAGATTACTGAAAG | 5521 |
rs191720012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146924123 | AATAACTAATGGGTA[C/T]TAGGCTTAATGCCTG | 5521 |
rs191721833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922683 | ACCTTTACCCATATA[A/G]CCCATGTGCTTGGAG | 5521 |
rs191724533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030380 | TCTAATAGTTTGCCT[A/G]TAAGTACTTTCATAT | 5521 |
rs191727328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959590 | CTGCAGGCAGGGTTG[G/T]GGGGCAGGAGCTAAG | 5521 |
rs191732090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997233 | GCAGCCATGGAGATA[A/G]GTCTGAAAAAGAAGG | 5521 |
rs191732458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794806 | TAGTGATATGACTAA[C/T]CATATTAATATGGTG | 5521 |
rs191734202 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892944 | TGCTTGTTTTATAGA[A/C]CCTCTAGGATCTATT | 5521 |
rs191738732 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741014 | CGCACTCTAGCCAAG[C/T]GACAGAGCAAGACTC | 5521 |
rs191739463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837192 | CATTGTTTTTTCACT[C/T]TCAGTACAGTATTCA | 5521 |
rs191754241 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726288 | TTAAGCCAACTAGGG[A/G]GTATTCAGCATCTAT | 5521 |
rs191764291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809585 | AAATGACGTATCAGC[C/T]AAAACTGGAAGGACG | 5521 |
rs191773604 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806500 | AAAAGAGGTACCTGA[C/T]TCTTTCCATTCCTTC | 5521 |
rs191778810 | snp | C/T | 0.0164022 | 0.089062 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591149 | GTGGTTCCCCTGGAG[C/T]GGGGGGCTCCTACTC | 5521 |
rs191782780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833366 | TCATTGTCATCTTTA[A/G]GCCTTTCACTAGTCA | 5521 |
rs191804622 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714596 | GCCAGGAATGAGGAC[C/T]GGTCGCCACTAACAT | 5521 |
rs191806711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740431 | CCACCATGGGAAGAG[C/G]CTGTTGTAAATGAAG | 5521 |
rs191808856 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802350 | CCCAAGAACTCAACA[G/T]GGGGGTGGCAAATGA | 5521 |
rs191808956 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772947 | AAGGCTCCTCTGCCT[A/G]TAAAGGACAAGACTT | 5521 |
rs191824548 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738753 | GACCATACTTCTCAG[A/G]GAGGATATAGGTAGA | 5521 |
rs191855925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696860 | ATTAAATAACTTTCC[A/G]CTTTTTTCCATAAGA | 5521 |
rs191862910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681711 | AATCAGGTTTGGAAT[A/G]GTGACAAGATCCTTA | 5521 |
rs191863126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648410 | AACGAACCTTCAGAG[C/T]TTTACTATAACTCTT | 5521 |
rs191865391 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648046 | CCATGGTGGAGACTA[A/G]CTAGCTGTGTACCAA | 5521 |
rs191868260 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044239 | AGTAGTTCTAAGAAA[C/T]AGATTTCAGTGCAAT | 5521 |
rs191873511 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662643 | CAGTCTGTGGTATTC[C/T]ATTATACAAACACAA | 5521 |
rs191880925 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014898 | AATAAAAAATAAAAA[A/T]TAAAAAATAAAAAAA | 5521 |
rs191881641 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060486 | ACAGAAAATTATCCA[G/T]GTGTGGTGGTACCCA | 5521 |
rs191883987 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616516 | TATAGAAGGAGCTCA[A/T]ACAATTCTATAGGAA | 5521 |
rs191885341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648763 | CATGTGAATGCTGTG[G/T]GCAAAATATTCTAGA | 5521 |
rs191886883 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634462 | GCCTCAGCCTCCTGA[A/G]TAACTGGGACTACAG | 5521 |
rs191888461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993011 | GCAATGACATGATCT[C/T]GGCTCACTGCAGCCT | 5521 |
rs191896382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617625 | GATATACCATGCCTA[C/T]GCTCCTTCAACAAAG | 5521 |
rs191910573 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051855 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 5521 |
rs191914680 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979998 | TGTTTTATTTTTTAA[C/T]ATGGCTTGGTGGTTT | 5521 |
rs191920681 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962653 | AAATAAAAATAATAA[A/T]AAAAAAACAACCTTA | 5521 |
rs191927516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969062 | CACTGGTTAGACATA[C/G]GCTCCTACTTGAAGA | 5521 |
rs191929451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006405 | TTCAACAAAAGTAAA[G/T]TTTGCTAAAAAAGTT | 5521 |
rs191936801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025233 | ACTGATATGTAAAGA[A/G]TCTGAAAATTCCTAT | 5521 |
rs191943502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068830 | ATTGGTATAGACCTG[A/C]CAACATAAAATTACC | 5521 |
rs191943655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993687 | AAAAATGATGGCTAT[A/G]GTAACTACCTTAAAG | 5521 |
rs191947645 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990607 | AGGCTTAAAACTATG[A/C]AACTATTAGTAGAAA | 5521 |
rs191964400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933574 | TTTATTCTGAAATTT[A/C]TACTTCAGGGAGATT | 5521 |
rs191968206 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594001 | TGTTTAGGGAAAGAG[C/T]AGATAGGACTTGGGT | 5521 |
rs191969572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022886 | CCCTCAAAAATGAAG[A/G]CAACATAAAGAACTT | 5521 |
rs191971689 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147058084 | TGAGGGGGAGATCAA[C/T]GTCTAATTCATCTTT | 5521 |
rs191973272 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918454 | AAATAGGTACTAATA[A/G]TAGGCTAAGCATTTG | 5521 |
rs191974089 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872923 | ATGTTCTTATCTGAG[A/G]CATCTCATCTATTCA | 5521 |
rs191979801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901133 | ACAAATTGAGGCACA[C/T]CCAGTTTTGAAGTTG | 5521 |
rs191988580 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878510 | CTCCTCCCCCTGGGA[A/G]AGCGGGCAGCCGCGA | 5521 |
rs191989630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812882 | AGACTTACTCACTAC[C/T]ATGAGAACAGTATGG | 5521 |
rs191996175 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841679 | TCAGCAAACTAACAC[A/C]AGAACAGAAAACCAA | 5521 |
rs192001314 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896999 | AAATTAAGGTCAATG[A/G]TGAACTGAGCATATA | 5521 |
rs192005917 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831454 | GTGAGCCGAGATTGC[A/G]GCACTGCACTCCAGC | 5521 |
rs192007318 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779313 | AGACTGTCCACATCT[C/T]GTTTCCAGAAAACGG | 5521 |
rs192011932 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937131 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 5521 |
rs192015410 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740537 | TCTTTCTTTTCCACA[A/G]ATTTGGATCTGCCAA | 5521 |
rs192021412 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885559 | AGCCACAAATAGTTT[A/G]CCAGTTCTTCAAAAT | 5521 |
rs192023776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848769 | CACCCTTAAGGCTTA[C/G]GGAGCTATGCCAACT | 5521 |
rs192025025 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906130 | GTCTGAGTTGAGATA[C/T]GTTGGAAGTGTAAAA | 5521 |
rs192030536 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864648 | CAACTGAATCCCAGG[A/G]TACAAACTACTCACC | 5521 |
rs192033316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758118 | TTCTTTGTGACAGGC[C/T]ACCCCTTCCTCTCAA | 5521 |
rs192033578 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725324 | GATATAGTTTTATTG[A/C/T]GAAAATGGAAAGTAA | 5521 |
rs192042509 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070191 | TAGAATGTGAGCTCC[A/G]TTAATACCACAGACC | 5521 |
rs192043594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784485 | ATATTTTTACCCCAC[C/T]ACAATCTTATTTATC | 5521 |
rs192047628 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819500 | ATGGCAAAGTGTCAA[C/T]TCCTGACCTTCCTAA | 5521 |
rs192052595 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804717 | ATATATTAGACATGA[A/T]TCTCTTCAAACTGGA | 5521 |
rs192053047 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752480 | ATTCATTTTATTTGA[C/T]TCATTTATCATCCGG | 5521 |
rs192055374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053393 | GAGTTTCTCTTAAGG[A/C]GATTGTTTGGGCTAT | 5521 |
rs192055387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707168 | GAGTCTCCAGCTGCC[A/G]CCTAAGGCTGTTGAT | 5521 |
rs192060682 | snp | C/G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679124 | AAGCTGGAGGCATCA[C/G/T]GCTACCTGACTTCAA | 5521 |
rs192062369 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674518 | CCTACATCCCTTTGT[A/G]TACTGTCTTGATGCA | 5521 |
rs192065486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683717 | CCAAAGGCGAAACAT[A/G]TCAAAACACAAAGGC | 5521 |
rs192066753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688219 | TACTGGTATTTATAA[A/T]TATATAGCAAATATA | 5521 |
rs192071626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655712 | AAGGCACACTCAGAT[A/G]CTTGGGAGGCAGACA | 5521 |
rs192082995 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821584 | GGCAAACAGAGTTGG[G/T]GTGAAACCTCAGTCA | 5521 |
rs192086230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642035 | TGACCTGACTGCTTA[C/T]GGCATTTCTTATTAA | 5521 |
rs192092517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649882 | AGAATTGTTAGCAAA[A/G]TTCTGTTTCTGGATG | 5521 |
rs192099632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997082 | TCTAGATTTTTTCCA[A/G]TTTACTTCTACCAGT | 5521 |
rs192104347 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029602 | ATTTATATATTAAAA[A/C]CCTAACCTCCCAATG | 5521 |
rs192106053 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001565 | ACTGTAACACTCACT[C/G]TGAGGCTCTGAGGCT | 5521 |
rs192108899 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757888 | AACTTCCATTTTCCA[C/T]AAAGCTTTGAGGCCA | 5521 |
rs192113527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064676 | ATACAAATCAAAACA[A/G]TCTAGCATATGAAAC | 5521 |
rs192140820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036652 | GTAAAAGCATTCCTT[A/G]TTCTCCACAACCTCA | 5521 |
rs192142557 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018458 | CTTTAAAAGATCTCA[C/T]TTTTTATATATATTT | 5521 |
rs192168151 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969320 | TGGAGTGAAACCAGA[A/T]CACAGAAACTTTTGG | 5521 |
rs192172620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914925 | TTCAGTATTCGAATC[A/G]ACAGTGGCTTCCAAA | 5521 |
rs192176492 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632773 | GGCCAGACAGGTAGA[A/G]TGTGTGGGGGGCAGG | 5521 |
rs192177248 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617042 | GTACTATTCAGCCAT[A/G]AAAAAGAATGAGATC | 5521 |
rs192177873 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882778 | TCTAATTTACAGTTT[A/G]TGTAAAAGGGGCCAT | 5521 |
rs192191733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653191 | TAGCTAGGTTTAATT[C/T]GGGGACTGGAAAGTG | 5521 |
rs192199749 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032940 | AATTTCCAAACTCTC[C/T]TTATTGTTTTCCATA | 5521 |
rs192210219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799530 | CACAATGGCATGGTG[C/T]CAATCTAGCCTGAGA | 5521 |
rs192211008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947446 | TCCTGTTTTTTCTGG[A/G]ACTGTTGGAGAAGTG | 5521 |
rs192213139 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930299 | GACAGATGTGTCAAG[A/G]GAGGAATAAGCTTGG | 5521 |
rs192225277 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762276 | AGCAGTTATGAACAA[C/T]GTGGACTCAATGGGA | 5521 |
rs192226870 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914263 | TAAAGAAGACCTTCT[A/G]TTATGAGCAAGATGA | 5521 |
rs192229222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005908 | AATTGATAATTGAGG[G/T]TCTTCTCTGTAACCC | 5521 |
rs192232117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068204 | CACTCTGTGTCAAGC[A/G]CCGTGCTTTGTGTCG | 5521 |
rs192235989 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979053 | ATTTAAGAATGGCTT[C/T]GTTTCTCTCTTTTCC | 5521 |
rs192247959 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729863 | CAGGGCCCTCATGGA[A/G]AACCTCTGCTAGGGC | 5521 |
rs192258937 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962354 | AAAGAGAATGTGTGT[A/G]CATTAAAACCAGACA | 5521 |
rs192259457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813357 | TGTCACTAAGAATAA[A/G]TATTACCTCATGCCC | 5521 |
rs192264811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867645 | GTCTAGAGCCAGGTG[A/G]GCTCTGATTCCACCA | 5521 |
rs192265469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827896 | AAGCCCTTTTTCTGT[C/T]GTCTTCCTACACTTT | 5521 |
rs192267596 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842679 | CCAGTGTGTGTTGTT[C/T]CTCTCTATGTATCCG | 5521 |
rs192273342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882169 | GTAGTCCCAGCTACT[C/G]GGGAGGCTGAGGCAG | 5521 |
rs192277178 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779515 | AAGGCCGGTTATTAC[A/C/T]GAGGTGTAGTTTCCC | 5521 |
rs192282674 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761751 | TTTCTGATCAATAAG[A/T]TGGAAAATAATAATT | 5521 |
rs192286524 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897996 | TTGAGACCAGCCTGG[C/T]CAGCATGGCAAAACC | 5521 |
rs192287035 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799003 | AAAATAGGTGACAGA[C/T]ACACTGAATACTCCG | 5521 |
rs192288876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721795 | CTGGCACTGAGCCAC[A/G]CATACCTCTTAAGTA | 5521 |
rs192295389 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858870 | TGGCAAGAGTAACAA[C/T]GAGTGACTTTAGGAA | 5521 |
rs192297049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737297 | GGTGTCTACTTCATG[C/T]AAAGACCTAGAGTGG | 5521 |
rs192301020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667734 | TGTCTGTCTTGCTTA[C/G]GGGCCACCTGGTCTC | 5521 |
rs192324399 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637379 | GTAAGGCCACAGATG[C/T]TGCTAAACATCCTAC | 5521 |
rs192327383 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827360 | ACAAAAAATGTAGCA[C/T]AGACCATAGATCAAG | 5521 |
rs192338196 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880504 | AGTAGGAGCAGAGTG[G/T]GGAAAAGCTAAGTTC | 5521 |
rs192339270 | snp | C/T | 0.000168745 | 0.0091839 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600244 | GCTGACTTAAAAGCT[C/T]ATGAAGGGAATGTTC | 5521 |
rs192348215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716735 | TTCCCTTCTAACACC[C/G]AGTTGAAAATTATTC | 5521 |
rs192355462 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733676 | AGAAGGTCATAAGTA[C/G]ATCTGGGGCAAGGAA | 5521 |
rs192356595 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655124 | CCCCGATTCAGGTGC[C/T]TCACCCTCCTCTCTG | 5521 |
rs192356897 | snp | C/T | 0.00333951 | 0.0407259 | utr-variant-5-prime, intron-variant | PPP2R2B | GRCh38.p7 | 5:147081294 | GAGACCCTAGTGAGT[C/T]CTGAGAGGACGGTCA | 5521 |
rs192358620 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697399 | CATCCTCTCTCTCTG[A/G]CCTATTTATGTCAAC | 5521 |
rs192364081 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018000 | TAGGAAATCTTCCAG[A/G]CCCAGATGAATTATA | 5521 |
rs192369319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641746 | CCATGTTTTCAGCAT[A/G]TGTAATTTTGCCCTT | 5521 |
rs192369687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049930 | CAGGTGATGGGGCAG[C/T]GGGTGAAGGAAGATA | 5521 |
rs192370801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798225 | CCAATTTCTTTCACT[C/T]GGTTGCCTCATTTTG | 5521 |
rs192377755 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624092 | TCATTGTCAGTGTTT[C/G]AGACTTAATGTTTTC | 5521 |
rs192380740 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682232 | AGCGTAGGAGAGTCA[C/G]TACAAAGGCAGATTC | 5521 |
rs192384528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605685 | CAGGGGGCATGACTG[C/T]CCCTGGTTGAGAATC | 5521 |
rs192405943 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735592 | GAAAAAAAGAGTCTC[A/G]CACTCAGGTATAATG | 5521 |
rs192407940 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955403 | TAGACTACATTTTGA[G/T]TAGCAAGTAAATAGG | 5521 |
rs192411519 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952088 | GTAATGCTAAGATTC[A/T]ACAAATAAAATTCTA | 5521 |
rs192413403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938966 | TTTGTATTTTAGTAG[A/G]GACAGGGTTTCACCA | 5521 |
rs192417780 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923093 | AGCTTTGACAGCTCC[A/T]GGTTTTTCCGCTACA | 5521 |
rs192427524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001251 | GCTGTGGAAGTTTTG[C/T]TCTTTCGCTCTTCAC | 5521 |
rs192435771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969534 | TTATCAGATCATTCC[A/G]CCTGTGGTATAGGAA | 5521 |
rs192436682 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700277 | GCTACTAGAACACAG[A/C]CTGGCCTGCTGGAAG | 5521 |
rs192440163 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986571 | TCAAAGATATTGAAG[C/T]ATTAATAAAAAAACA | 5521 |
rs192449775 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830896 | TTCAGTTTATGATGA[A/G]CCAATGTGTGATGGT | 5521 |
rs192456034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665970 | ACCTTTAACTTGTAA[A/G]AAACATACTATCTGT | 5521 |
rs192460376 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894025 | CACTCCAGCCTGGGC[A/G]ATAGAGTGAGACTCA | 5521 |
rs192462971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863658 | TCCATCCATCCATCC[A/G]TCCATCCATCCATCC | 5521 |
rs192485189 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008056 | GATTCTTCTTATTTA[C/T]TGAACATCAATGAAA | 5521 |
rs192485522 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897875 | AGAAGGTTAAAATAT[A/G]CTGGTCAAGGAAATC | 5521 |
rs192495017 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048291 | CTCTGGAGTCAGGCA[A/G]TATGGGTGCATACCC | 5521 |
rs192495760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594455 | CTGGGTTCTCTGTTT[C/T]GAAGGTAATCCTTCC | 5521 |
rs192501356 | snp | A/G | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082011 | AGTTTTCTTCTCAAC[A/G]GCATGAACATTCCCC | 5521 |
rs192501777 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866970 | GCAAACTTCTGCTCC[G/T]TCAGGTTGAGTTGCA | 5521 |
rs192506624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881757 | ACTTAGTAGATGCTT[A/G]ATTATATTTGTTGGA | 5521 |
rs192525736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834462 | CTTTTGTTTTGGTTT[A/G]GCTATAAATATTTCA | 5521 |
rs192528749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852666 | CCACCTCTCTCCAAA[C/T]ATTCTCAACAATTCC | 5521 |
rs192537654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711680 | GAGATGAAAGGACTC[A/G]ATTTAATGAATGCCT | 5521 |
rs192540954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788086 | GAAATGAGAATCCCT[A/C]CCTCTGCCTCCTCCA | 5521 |
rs192544031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930790 | CTCATTTCTCTTTGT[C/T]GATATTAGAATTTTA | 5521 |
rs192549059 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780749 | TTCCTCAGTTGCTAG[C/T]CCATGAGTCCATGAC | 5521 |
rs192552552 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955074 | AGTCAGGTTGAATTA[G/T]TTGGCCATTAACTCA | 5521 |
rs192553791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822211 | TCAATTTAGAGCAGA[A/G]CCTTGCAAATGAGGA | 5521 |
rs192555003 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807842 | TTTGCTCTTGTTGCC[C/T]AGGCTGGAGTGCAAT | 5521 |
rs192568495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676747 | GAACCATATCTTTCA[G/T]GTTCACTTCTATAAC | 5521 |
rs192569692 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898326 | GTTACTGTAGCCTTG[C/T]AGTATAGTTTGAAGT | 5521 |
rs192572569 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021553 | ACCACCCCAAACTGA[A/G]AGAGCTTCCATGTGA | 5521 |
rs192579883 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645568 | TCCCACTGAATTAAA[A/T]GGAAGCTGCTGTCCA | 5521 |
rs192596675 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608689 | AGTCCCAGCTACCTG[C/G]GAGAAGAATCGCTTG | 5521 |
rs192600920 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056530 | AATAGAAAGCCACAA[C/T]GCAAGAATAGAGACT | 5521 |
rs192607341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814349 | AGGTCCTTATGTTAC[A/C]GTAGGTAGCTATTCA | 5521 |
rs192610284 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076129 | CACTATATCACACTG[C/T]GTTTCCTGGATAAAT | 5521 |
rs192619807 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676331 | AGTTCCTTAACAAGA[C/G]CTATGGTGCCCAGCA | 5521 |
rs192622475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651262 | TAATCGTCCAAATTC[A/G]GCCACTAATATATAG | 5521 |
rs192624563 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637811 | TTTATTGCCAAGATC[A/T]GTGCAGTACTGTGCA | 5521 |
rs192633238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658032 | ACTACATGCTGAGAA[A/G]TTGCCACACAGAGTA | 5521 |
rs192634769 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620778 | CCCTCCTTCCCTCTC[A/C]TAATTTGTTCCCAAC | 5521 |
rs192642832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600836 | ATACAATTCACATAC[C/T]ACAAAATGTAGAGTT | 5521 |
rs192649889 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989542 | AGCCTTCAATAAAAT[G/T]CAACATCTATTCATG | 5521 |
rs192651428 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780133 | TTTATTTTGGACCTA[A/C/T]TATGTGGCCAACACT | 5521 |
rs192666321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744551 | AAATGTGAAATTCCA[C/T]TCCTACCCTCACATG | 5521 |
rs192673567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712025 | TTTGTTAAACTGTAG[A/G]TGGGCCTAAAGAAAT | 5521 |
rs192691192 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003039 | AAAATGGCCACCTGA[A/G]GGAAGTATAAATTAC | 5521 |
rs192691766 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933734 | ATGTGCACATTGTGC[A/G]GGTTCGTTACATATG | 5521 |
rs192695380 | snp | C/T | 0.000188023 | 0.00969413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040694 | CCTTGTTAGGTACTC[C/T]GTGTGAGGAAGGTAG | 5521 |
rs192696348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871102 | CTGATTCTAGAGTTC[C/T]ATTGGAGTCAAAAGA | 5521 |
rs192701412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021304 | CATGACAGTCTTACT[C/T]AGCTGAGGAGACAGA | 5521 |
rs192702869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901549 | CCTACATTTCCAATG[C/T]TATTTCAACCTATCT | 5521 |
rs192705601 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684652 | TGAAAGCCCATCTAC[C/T]CTCCAGATGCATCGT | 5521 |
rs192708912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651130 | GTCTAGTTCAACTTT[A/G]ATCTAAATTTATCTT | 5521 |
rs192719749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620346 | CATTTATTAGCCAAG[C/T]GGGACTGGTGCCTTT | 5521 |
rs192722307 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997586 | TGCAGTTGATCTTGA[C/T]GCATGCCAACATGTG | 5521 |
rs192725306 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030695 | TATTAATTATTAAAG[C/T]CTAATTTATATTAGC | 5521 |
rs192727335 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817476 | ATCTTTTAATATATG[C/T]GTGCATTGTGAAATG | 5521 |
rs192735179 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749957 | TCTAAGTCTGTGATC[A/C]ATTTTGAGTTCATTA | 5521 |
rs192738229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783585 | TGCTATTTTAAAAAA[C/T]AATTAATGTCAGAGG | 5521 |
rs192743111 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688609 | CTCCCAGCCACACCT[A/C]AGGGCCTCCTTCTCT | 5521 |
rs192754476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716170 | TGTTTACTGACTAAA[C/T]AAAAAAGTAAATACA | 5521 |
rs192757727 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656248 | GGAGTGGGGTATGAA[A/C/G]AGAGACCTGAATGAA | 5521 |
rs192758377 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966177 | CCTTTGGCTGCCTGC[G/T]ATATTAGTGTTGGCC | 5521 |
rs192762347 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933927 | ATGAGTGAGAACATG[C/T]GGTGTTTGGTTTTTT | 5521 |
rs192762827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625154 | TTTGCCTGCAAACAC[C/T]AAAACTTATGTTCTA | 5521 |
rs192766545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877880 | CGGGGCCAGCCGAGC[C/T]CCCGCCCCAGCCCTA | 5521 |
rs192779733 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910274 | CAGATAGAAAAAAAT[C/T]TGAAGGCTATACAGC | 5521 |
rs192780076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000874 | TTCTTCAACGCCTAA[A/G]GGGAATCTTTATGTT | 5521 |
rs192780841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847861 | ATGGATTTAGTAAAT[C/T]ACCCAGCCCCATAGC | 5521 |
rs192790539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948272 | TAAACACTGGCTCTG[C/T]TGCTTCCTAGGTGTT | 5521 |
rs192794318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034106 | AAACTAAGCTCTAGC[C/T]ACACTGCTCTGCTTT | 5521 |
rs192801873 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818282 | TGGCACATAAGACAG[C/T]CAAACGATATTTGTT | 5521 |
rs192805642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910797 | ATTTTTAAAAAGAAT[A/G]TAGTATAAAATCATT | 5521 |
rs192826803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729282 | AGAGATGATTTAGGG[C/T]ATCTGGCAGAAGAAA | 5521 |
rs192827884 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692755 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCT | 5521 |
rs192836770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658353 | TTATCACCTTGCCTT[C/T]TCACTGGGCTTCCTT | 5521 |
rs192845380 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041378 | ACCTGTAAGACCCTT[C/G/T]CTTCAGCATTCTGCA | 5521 |
rs192847297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824392 | AAGGGCAGATACTGC[C/T]GGTAGAGCAGCCATG | 5521 |
rs192848349 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629305 | TCAGTGTATGGTACC[A/G]TACAGTAACTCAAGC | 5521 |
rs192848802 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003553 | TTAATGAAAAGAATG[C/T]GGCTTTAGCTGCAGC | 5521 |
rs192853047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855057 | GAAATCCACTCAAAG[C/G]TATTCAGTTTCATCT | 5521 |
rs192861198 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734089 | AGACAGGGTTTTACT[C/T]TGTTGCTGAGGCTGG | 5521 |
rs192863248 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767690 | ATTATCAACAACCTC[A/C]ACCACAGTGGTTCAT | 5521 |
rs192864337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794524 | CTATAAATAAAATGG[G/T]TTGCTATGAATGCCC | 5521 |
rs192875946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951684 | GTCCCTGCAAAGGAC[A/G]TGATCTCATTCCTTT | 5521 |
rs192879170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976002 | ATTTGTCTACTTTTA[C/T]TTTTGTTTCCTGTGC | 5521 |
rs192903632 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855524 | CTGCTTTTTGTTTTC[C/T]TCCCTTTTTGAACTG | 5521 |
rs192905890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918815 | TTTTTTTCCTGAAGA[G/T]GCTATCTCCAGTTTT | 5521 |
rs192906246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986833 | TAGAAAAAGAGAAAT[A/G]GGTGGAAAGCTTATT | 5521 |
rs192907172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606493 | GCTTCATTTAATGGA[C/G]ATAATAGTAGTACCT | 5521 |
rs192910365 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633428 | AGGATGGAGAAAATC[A/G]ATATGAAATGTCAGG | 5521 |
rs192910989 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886070 | GCGGCCGGGCGCGGT[A/G]GCTCACGCCTGTAGC | 5521 |
rs192913232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006301 | TACAGAATCAGGAAG[A/G]AGCCATCTATACCAA | 5521 |
rs192921682 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043538 | GAGAAAATAAACTAC[C/T]GTTGTTTAAGCCACC | 5521 |
rs192922755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080057 | AGAGTATTTGGTTTT[C/T]GGTCACCCACTATTA | 5521 |
rs192931136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804092 | GAATCGCTTGAACCC[A/G]GGAGGTGGAGGTTGC | 5521 |
rs192936348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830336 | TAATGCCTATAAAAA[A/G]CTAGCTGTTAGGATT | 5521 |
rs192937616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765506 | ATATTATGAGAAGTG[A/G]CCAAAACCCTTTGTG | 5521 |
rs192945571 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707463 | ACCATAGGCCACCCC[A/G]GAAGCTGCTGCTGCC | 5521 |
rs192952769 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733099 | TTGGACTTCTAGGTC[A/G]CCATGAACTCTCAGC | 5521 |
rs192953395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889602 | TCCAACAATTGAAAC[A/G]TTGCAATTGGAACTC | 5521 |
rs192961824 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674708 | GGGCTGGACAAACAT[A/G]TGGCTCCCTTTCAAT | 5521 |
rs192965288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642523 | AATTTTTATATATCT[C/G]ATTAAATTGTTTTTG | 5521 |
rs192966758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859333 | TTACATAACTCCTTC[C/T]TTGCCTAATATTTAG | 5521 |
rs192970208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080622 | ATATGCTAAGATTGG[A/G]ATTCAATGTTCTCGT | 5521 |
rs192973685 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835477 | TAGCAAACATGTACA[A/T]CTTTGGTTTGTCACC | 5521 |
rs192983013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771247 | GTGAAATACCTCTTT[A/G]ATGCTTGTTCATCAC | 5521 |
rs192983815 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808121 | CTCTTAAATATTCTC[A/T]CTCCACCTTTGTGTC | 5521 |
rs192991785 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016425 | GTTTTACTTCTAAGA[C/T]GTTGTTAGCATAGAA | 5521 |
rs192994629 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986040 | AATTCATGTAAGACA[A/T]CACCTTCACAAGAAC | 5521 |
rs193009088 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052780 | TAAATGTGAGTGTTT[A/G]TGTTTTAGAGTGTGG | 5521 |
rs193016962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894167 | TCTGGGCAAATATTC[C/T]ACCTCCATGTTACCA | 5521 |
rs193026746 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649471 | TTTTTTTGAGATGGA[A/G]TCTGGCTCTGTCACC | 5521 |
rs193030066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926384 | TGATTTTATTTATTT[A/C]TTTATTTATTTACTT | 5521 |
rs193031407 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673250 | ATCTTACCACAGATG[C/T]TGGCGGGATGATTTT | 5521 |
rs193036502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053020 | CTAAATACAAGTGAA[A/C]GCTGGTTATTACTAT | 5521 |
rs193056138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838715 | TAAGAAAGTGATATG[C/T]TAACACATTAATGAT | 5521 |
rs193060062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751259 | AATAACAGTGCAGAG[C/T]TCTACTTCCGGGCAT | 5521 |
rs193060400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961649 | TGGTGATGCCTTTTA[C/T]ATGTTAAGAGTATTA | 5521 |
rs193063445 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774350 | TTTTGTCTTAAACTG[A/C]CCAAAAAATAATAAA | 5521 |
rs193091973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906794 | TTGGGCAGTACTGTT[C/T]TACCTCATGACTGTG | 5521 |
rs193093009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843893 | CTTTGTTATTGTGAA[C/T]AGTGCCGCAATAAAC | 5521 |
rs193095081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929618 | ATAGTAAAAGTTATG[A/G]GAAGTCCTACAGGAA | 5521 |
rs193096677 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874454 | TATAACCAGGAAGTA[C/T]ATTAAGTAACAATAA | 5521 |
rs193102566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814816 | GACAACATGGAAAAA[C/T]CCCAAGTCAAAAGTC | 5521 |
rs193117058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754225 | AGCAATTCTGCATCA[A/G]TGCATTTTTACTAGA | 5521 |
rs193119874 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720686 | ACAGATATTTATTAA[C/G]GTTTTATTAAGGACT | 5521 |
rs193121808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684979 | ATTGAATTCATTTTA[C/T]GTTTCAGCCACTTGT | 5521 |
rs193125543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031211 | CATGGCACTCCAGCC[C/T]GGGCAACAGCGAGAC | 5521 |
rs193134877 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067087 | AGTTGTCTACATTTA[C/T]GGTGTACAACATGGT | 5521 |
rs193136729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628763 | TGCTAACTGCTTTTA[C/T]TTAAAGTAACTAATT | 5521 |
rs193144954 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974275 | CTGTGTGCTTTATAC[C/T]GTTCTAAGTCCTTTA | 5521 |
rs193154027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624574 | TTCTCCCAGCATCTA[C/T]TCTTCCTCCTGAGGC | 5521 |
rs193155894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024770 | TATTTCAACTAAGCA[A/G]TGATGACAAAACAGT | 5521 |
rs193158430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993353 | GTTTGAGCAATCCTC[C/T]TACCTCAGCCTCCCG | 5521 |
rs193160373 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970205 | TTCCTCAAGGCTGCA[C/G]AGTAAGTGGCAGTGC | 5521 |
rs193160823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059840 | CCAGCTAGAGCCCCT[G/T]CCTTGGGGCCAATAG | 5521 |
rs193186258 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822612 | TTGTTTACCACCCAC[A/T]CTCTATATCCTTAAC | 5521 |
rs193189456 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873167 | GCAAAATTCTGGGAG[C/T]TGTCCTTGACATCAC | 5521 |
rs193191781 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853090 | CTAACATAGCAGTTG[A/C]CATTTAGGAGCAAAC | 5521 |
rs193193052 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788821 | TGCAACAACAGAAAC[A/G]AAACTCTCTGCCTTG | 5521 |
rs193202549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754823 | TCCAGGCAACAGCTG[C/T]GTTGGTGAGCCATGA | 5521 |
rs193211964 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663471 | CATCCTATAAAAACA[A/T]CCGTAAATAACAATA | 5521 |
rs193212798 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725030 | ATAATTCTAATTCAT[A/G]TATACTTCTATTAAT | 5521 |
rs193216237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687462 | GAGAGTGCAGCGTGG[C/T]GCATGGTATATGGCA | 5521 |
rs193216600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035072 | TCATTTAACATCATT[C/T]CCAGAAGGAAGGTGC | 5521 |
rs193217829 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635030 | GAATCCAGGGTGAAT[A/C]ATTGTGATAACTGCT | 5521 |
rs193221846 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596029 | TTTTCTCCAAAGGGC[C/T]GGATAGTAAATATTT | 5521 |
rs193225413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069243 | TACTATGAGAGGTGA[A/G]GTATGAAGAGCTCTA | 5521 |
rs193234063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978510 | GATTTTACGTACTAC[A/G]TTTAAGTCTTTAATA | 5521 |
rs193247512 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946496 | GTCCCAAGTCTGTTG[C/T]TTAGTCTCAGCATCT | 5521 |
rs193251403 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890402 | TCACCTACACCATCA[C/T]GGTTTGCCACACTCT | 5521 |
rs193253296 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913483 | AGAGGCCAACATATA[A/G]TTCCAGTAATGACTG | 5521 |
rs193256205 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800635 | AATTTTTTTTGGGGG[G/T]TGGGGGGGTGGACTA | 5521 |
rs193258732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828385 | TGGGTGAGATCTACA[A/G]ACTAGAATCAGGGCT | 5521 |
rs193268970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770845 | CAATGAGGCTCAAGC[A/T]GTTGCAGAGGGGATT | 5521 |
rs193270104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736725 | CTGACTCCGGTGTAA[A/T]CTGTTAATTACTATT | 5521 |
rs193272796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703701 | TCTCACTTTAAGACC[C/G]ATGCAAGTCAAAACA | 5521 |
rs193278568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668553 | ACTGAAGAAAATTAC[A/G]TAATTACTTCTTCTG | 5521 |
rs193283356 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050588 | AGCTGTGTGAACTTA[C/G]ACTACTTAACTTGTC | 5521 |
rs193286519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644695 | AGTCATTTTATCTCT[C/T]TGGGTTTCCATTTCT | 5521 |
rs193291071 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989162 | CTTCACTGTTGAATT[C/G]TACCAAACATTTAAA | 5521 |
rs193291963 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608550 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 5521 |
rs193295056 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959044 | GTAGCCTTAATCTAA[C/G]CAAAGCCAATATTTT | 5521 |
rs193922942 | microsatellite | (CAG(7_28)) | | | | | GRCh38.p7 | 5:146878729 | AGTGC[(CAG(7_28))] | 5521 |
rs199509852 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940245 | TACAAGTCTCAGAGC[C/T]CTGCCCTCCTGGCTG | 5521 |
rs199510591 | in-del | -/CTG/GCCCTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677059 | TCTTTGTTGTCTGCT[-/CTG/GCCCTG]TTGTCTGCTTTGACG | 5521 |
rs199518697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593071 | CATGAACCTGGAGAG[C/G]AAACATATCGAGAAG | 5521 |
rs199522593 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745962 | GACTTGGTCTCAAAG[A/G]AAAAAAAAAAAAGAT | 5521 |
rs199540016 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734071 | GTTTTTTTTTTTTTT[G/T]TGAGACAGGGTTTTA | 5521 |
rs199549161 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679235 | AGCCCTCAGAAATAA[C/T]GCTGCATATCTACAA | 5521 |
rs199561605 | in-del | -/GTGT | 0.496616 | 0.0409947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808959 | CAGCTGCTAACACTG[-/GTGT]GTGTGTGTGTGTGTG | 5521 |
rs199563242 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643207 | GAGAGAGAGAGAGAG[A/G]GAGACAGACAAGGGC | 5521 |
rs199567203 | in-del | -/TG | 0.214843 | 0.247516 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812769 | ACTAGAGTTACTTAA[-/TG]TGTGTGTGTGTGTGT | 5521 |
rs199602037 | in-del | -/CT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938442 | AAAAGATTCTGCAAA[-/CT]CTCTGACCTAGCAAT | 5521 |
rs199602304 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016551 | AGTCTGAGAAAACAT[-/A]AGGGGACACAGTCAC | 5521 |
rs199612936 | in-del | -/TCT | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052130 | TGGCTTCTGTTTGTA[-/TCT]TCTTATTTCAAGTTA | 5521 |
rs199615922 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908526 | AAAGAAATTGTTAGA[-/T]TTTTTTTTTTTTTTG | 5521 |
rs199626566 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615531 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAACTATT | 5521 |
rs199629439 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647219 | TGTTTTTTGACGTTC[A/T]CTATTGCTTAGAAGC | 5521 |
rs199653364 | in-del | -/ATTC | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912820 | CTCTTTCAACTTTTG[-/ATTC]ATTCATTCATTCATC | 5521 |
rs199664920 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005332 | AAGTAAACCTCTTCC[C/T]CCAGGGACCAGTGCC | 5521 |
rs199681311 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626718 | AACCCTATGGCCAAT[C/G]TTTCCCATTCTGCAT | 5521 |
rs199686863 | snp | A/G | 0.000245373 | 0.0110737 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590250 | CAGAGAGCAAAGGCA[A/G]TGACATATCTTCACT | 5521 |
rs199687353 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737596 | TTTGATCCATTCCGC[-/T]TTTTTTTTGCCACAT | 5521 |
rs199700885 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025880 | AGAACATAAAAAGAT[A/G]CCCTGCTTCCTTAGT | 5521 |
rs199731541 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775090 | TTCTCAAACTCTTTC[-/A]AAAAAAACGAAAACA | 5521 |
rs199758783 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625317 | GGTATTTTATTATAC[-/TG]TGTGTGTGTGTAATG | 5521 |
rs199767151 | in-del | -/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670451 | TAGTACCCCTTCAGA[-/TTT]TCTTATCTGTTTTAT | 5521 |
rs199772019 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737809 | GCCAGGTGTGGTGGC[C/T]CACACCTGTAGTCCC | 5521 |
rs199774873 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883925 | TATGAAAATACACAG[G/T]GGTACACTGAAGCTG | 5521 |
rs199788697 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012160 | AAGGAATGGTACCAG[C/T]TCCTCCTTGTACCTC | 5521 |
rs199801178 | in-del | -/AA | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973751 | CTTATATTTTTAAAA[-/AA]CATCTTTGACAAGGT | 5521 |
rs199805094 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915477 | ACACACACACACGTA[C/T]ACATGTGTGCAATTT | 5521 |
rs199805359 | in-del | -/AA | 0.110494 | 0.207456 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022558 | AGCAAGGCTCCATCC[-/AA]AAAAAAAAATCCAAA | 5521 |
rs199805998 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831245 | CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 5521 |
rs199858377 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764810 | TATCCCGAGAGAGAG[A/C]GAGAGAGAGAGAGAG | 5521 |
rs199874569 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936528 | CAAAAAAAAAAAAAA[-/A]GAAAAAACAAGACAT | 5521 |
rs199878645 | snp | A/G | 0.000562281 | 0.0167578 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638376 | GCTGTGATCACCTCC[A/G]TGAGCTCCTCCATGT | 5521 |
rs199897541 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714813 | CTTGATTTTTTTTTT[A/C]TTTCTTCCTCCTTAT | 5521 |
rs199901617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696162 | AGGGTAGAGTGCGGT[A/G]GAGTGATCTCGGCTT | 5521 |
rs199901782 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659049 | AAATGATCAAAAACC[A/G]TTTAACATGATTTAG | 5521 |
rs199921203 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667331 | GAATAGGCGTGCGCG[C/T]GCACACACACACACA | 5521 |
rs199938289 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975502 | AGATCTTGCTTTTAA[-/T]TTTTTTTTGGCTATA | 5521 |
rs199943453 | in-del | -/CG/CGAGTATT/CGAGTATTACGGAGA/CGAGTATTACGGAGAAAGGCA | 0.000164564 | 0.00906984 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590254 | AGCAAAGGCAATGAC[lengthTooLong]ATATCTTCACTGTCT | 5521 |
rs199946273 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644312 | TTAAATTGTTTTTGG[C/T]TTTGGCTTTTAAAAT | 5521 |
rs199949881 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032189 | TACAACGAACTCAAA[C/T]AAATCAGTAAGAAAA | 5521 |
rs199952399 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838585 | CAAAAAAAAAAAAAA[C/T]AAAAAAAAGAAGGAA | 5521 |
rs199977884 | in-del | -/GA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764828 | AGAGAGAGAGAGAGA[-/GA]TACACGCACACACAC | 5521 |
rs199992384 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993808 | AAATATCCAGCACAG[G/T]TTTTTTTTTTAAATA | 5521 |
rs200019183 | in-del | -/A | 0.157972 | 0.232445 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643359 | ATCCATGGAGCCTAT[-/A]TTCTAGTAGGGAACA | 5521 |
rs200031908 | in-del | -/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985018 | AATATTTTCTTTTTC[-/TTT]TTTTTTTTTTTTTTT | 5521 |
rs200041252 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705753 | GGGGTTGGGGAGGGG[-/A]TAGGAAAAAAGTCTG | 5521 |
rs200044393 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911093 | TAGACACTTTCTTTT[C/T]TTTTTTTTGAGATGG | 5521 |
rs200045048 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752664 | CCCCAGGTTTTTGGG[-/GT]GTGTGTGTGTAGTTC | 5521 |
rs200059385 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014025 | ATCTACAATGAACTC[A/C]AACAAATTTACAAGA | 5521 |
rs200073644 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002953 | CAATTTGACCCACAA[A/G]CCCTGAAAAAGAGGC | 5521 |
rs200098016 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840227 | ATTGAGTTCCCTTGA[A/T]TATACATAACAAACA | 5521 |
rs200111570 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769355 | GGGTGTGGCAAATCC[A/T]TGTGTATTAGCGAGC | 5521 |
rs200116786 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728607 | TCCCCACTGAAATCT[C/T]AACTTGAATTGTATG | 5521 |
rs200121786 | in-del | -/TA | 0.0839998 | 0.186933 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077272 | ATATATGTATGTGTG[-/TA]TATACACACACACAC | 5521 |
rs200126115 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007782 | GACTGCGAGGGTCTG[C/T]GGCTTCACTCCTGAA | 5521 |
rs200135295 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840246 | ACATAACAAACATTT[A/T]ATTGAGTGACTCCTC | 5521 |
rs200143467 | snp | A/G | 9.8925e-05 | 0.00703226 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638348 | GTTGCAATGATGGGG[A/G]TGGAACTCGGCTGCT | 5521 |
rs200145860 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845320 | CTTTTTTTTGTTTTT[G/T]TTTGAGATGGAGTCT | 5521 |
rs200165671 | in-del | -/CTTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681932 | TTCTGTAATGTGATT[-/CTTTT]CTTTTTCTGACACTA | 5521 |
rs200174459 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902833 | CAAAGTTTTGCTACA[A/C]TGGAATCAGTTTATT | 5521 |
rs200175030 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146612985 | AAAGAGGGAATCCTC[C/T]CTAACTCATTTTATG | 5521 |
rs200183251 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812793 | TGTGTGTATATGTGT[A/G]TATATATATATATAT | 5521 |
rs200190167 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056667 | ACTGAGATTTCAAAT[-/GA]GAGAGAGAGAGAAAA | 5521 |
rs200196611 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668430 | TCCCTCATAATTTCC[C/T]CCCACTTCCCTGCCA | 5521 |
rs200201001 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663491 | AAATAACAATATACA[A/G]GCATGTCCCAGAGAT | 5521 |
rs200202899 | in-del | -/TAA | 0.029116 | 0.117091 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031511 | CTTGACTGGAGTTAA[-/TAA]CAGTTCTTAAATCTG | 5521 |
rs200206595 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733724 | ACACACACACACACA[A/C]ACACACACACGTCAT | 5521 |
rs200209710 | snp | A/G | 0.212425 | 0.24716 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678485 | TGGAAACTGGCACAA[A/G]ACAGGGATGCCCTCT | 5521 |
rs200234993 | in-del | -/AC | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005846 | AATAGTAAATAAAAA[-/AC]AGTGTACCCTATTCC | 5521 |
rs200245899 | in-del | -/TC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907480 | AAAGTGGAATTAATG[-/TC]CTTACAGAAGGGCAA | 5521 |
rs200253613 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794488 | AAGTGACTGTACTTA[A/C]AATAAACTGCCACAG | 5521 |
rs200272920 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075960 | TATATTTCTAATTAT[A/G]TTATCATAAGAATTC | 5521 |
rs200282006 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760990 | CACCAGTTAGAATAG[C/T]GATCATTAAAAAGTC | 5521 |
rs200287221 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593488 | CAGGTGACAGATTAT[A/G]TAACCAAGTAAATAA | 5521 |
rs200293913 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042226 | GTTTTAACTAGACCC[C/T]CCCCTCCCCTTTCTA | 5521 |
rs200297388 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951181 | TCTCTTTTTTGTTTG[-/T]TTTTTTTTTAATATC | 5521 |
rs200307570 | in-del | -/TTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795645 | GAGTAGATGTTATTC[-/TTG]TCATCACATATGCAT | 5521 |
rs200311487 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928281 | GGTTTATATATATAT[-/A]TTTTTTAGATCAGAT | 5521 |
rs200317606 | snp | G/T | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857704 | ATTTTTTTTTTTTTT[G/T]GAGATGGAGTTTTGC | 5521 |
rs200323077 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771843 | GGATGAGATACCCAA[C/T]ATCCTGGCCCATAAA | 5521 |
rs200347992 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592872 | AGGTTTTGGGGCCCA[A/G]TTTTGACCTCCCTTT | 5521 |
rs200351286 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003531 | TTGTTAGATCAAACC[A/C]TGGCCTTTAATGAAA | 5521 |
rs200375972 | snp | G/T | 0.1652 | 0.235179 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734061 | AATGAGTTAGGTTTT[G/T]TTTTTTTTTTTGAGA | 5521 |
rs200380168 | in-del | -/CCTCCCTT | 0.0675761 | 0.170943 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908777 | TTCTTCCTTTCCCGC[-/CCTCCCTT]CCTCCCTTCCTCCCT | 5521 |
rs200383673 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815070 | CAGTAGAAGGAGACA[-/TG]GAAGCCATCTATCCT | 5521 |
rs200384803 | in-del | -/AGAGAGAA | 0.499087 | 0.0213463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745201 | GAGAGAGAGAGAGAG[-/AGAGAGAA]AGAGACTATAAGCAT | 5521 |
rs200387646 | in-del | -/C | 0.0205511 | 0.0992634 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823238 | AGTCTTGCTCTGTCG[-/C]CCAGGCTGGAGTGCA | 5521 |
rs200387956 | in-del | -/TGAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013283 | ATGGGTAGGAAGAAT[-/TGAT]ATCGTGAAAATGGCC | 5521 |
rs200396472 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919277 | TTAGAGAAAAATTTA[A/C]TAGAAAAAGCTCCCA | 5521 |
rs200397351 | in-del | -/TC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848847 | CTGCATGGGAGATTT[-/TC]TCCTCCTCTCCTATT | 5521 |
rs200403461 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053230 | AAAAAAAAAAAACAC[A/G]CGCGCACACAAAAAA | 5521 |
rs200413956 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869055 | GAAAGCCCTCCATAA[C/T]TACCAGCAATCATTA | 5521 |
rs200428931 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675044 | CTCAGCTCACTGCAA[C/G]CTCCACCTCCTGGGT | 5521 |
rs200471600 | in-del | -/AAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053225 | GCATTAAAAAAAAAA[-/AAC]ACACGCGCACACAAA | 5521 |
rs200474240 | in-del | -/TC | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754670 | TGGCTTCCTTCTTGA[-/TC]TCTCTCTTTCATTCT | 5521 |
rs200478345 | in-del | -/AAAC | 0.494187 | 0.0535994 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898783 | AAATTTACAAGAAAA[-/AAAC]AAACAACCCCATCAA | 5521 |
rs200492908 | snp | C/T | 4.08422e-05 | 0.00451878 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055744 | AGAGAAGCATTTCAT[C/T]TTCCAAATAAAAAAT | 5521 |
rs200519564 | snp | A/C | 1.71021e-05 | 0.00292416 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146638440 | ACGAGTCAAGGAAGG[A/C]ACCAGGAGAAGGAGG | 5521 |
rs200522090 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772404 | TATATATATATATAT[A/T]TATATATATATATAT | 5521 |
rs200543782 | in-del | -/AAA | 0.0376037 | 0.131863 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881775 | ATATTTGTTGGAGAC[-/AAA]AAACATTTCTTAAAC | 5521 |
rs200547350 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005906 | ATAATTGATAATTGA[A/G]GGTCTTCTCTGTAAC | 5521 |
rs200551352 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038557 | TCAATGAGTGGCTGG[G/T]GCGATAAAAGGATGG | 5521 |
rs200556492 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037159 | TACAGTAGCTTCAGG[A/G]AAAAAAAATTATTTT | 5521 |
rs200557744 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053547 | TGCCAACAATATAAA[A/C]ACACACACACACACA | 5521 |
rs200575290 | in-del | -/GGTTTCCACATTTTTATAA | 0.0618563 | 0.164627 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590941 | ACTTAATGGACAGAT[-/GGTTTCCACATTTTTATAA]GGTTTCCACATTTTT | 5521 |
rs200580002 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940507 | GAAGAACATTTGCTA[-/G]GGGGAAAAAAAAAAA | 5521 |
rs200580497 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668191 | CTAAAGAAAACGATT[C/T]ATTCTCTAGCTTCCT | 5521 |
rs200580726 | in-del | -/TC | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889639 | GCTTTGCCTTATGCA[-/TC]TCTTTCTTTGGTTTA | 5521 |
rs200593451 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079318 | AAATTATGAACTCAA[C/T]CTAAGTGTTCATAAA | 5521 |
rs200619210 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901806 | AATCCAGTTATGTAA[C/T]GGTCGGTGTGATGAG | 5521 |
rs200619306 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827435 | ACCCAGAACACATCG[A/G]TTATTTTCAAAATGT | 5521 |
rs200624031 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641977 | CCGACAGCCAACAGA[A/T]TGCCATTAAATTAAC | 5521 |
rs200624539 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677044 | AACTCCTGAACTCCT[A/G]TCTTTGTTGTCTGCT | 5521 |
rs200625079 | in-del | -/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830462 | TACCTCACTCTTCCT[-/G]CATCTTGGTTAGCCA | 5521 |
rs200633880 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639337 | TCTGGGTTTTTTTTT[-/T]CTCAGTATTTCCCTT | 5521 |
rs200639066 | snp | A/C | 0.176219 | 0.238865 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626139 | TGTTTTAAGCCACTA[A/C]ATTTGTGAGAATTTG | 5521 |
rs200662520 | in-del | -/TATATATACTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812487 | TGATAGCAGTATATA[-/TATATATACTG]TATATATATACAGTA | 5521 |
rs200668612 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006340 | TAATATGGACTGAAC[A/G]AGGTCTTATTAATAG | 5521 |
rs200686296 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649589 | AACTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 5521 |
rs200709925 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680412 | GGGTGGGGTGGGGAG[A/G]GAGGGATAGCATTGG | 5521 |
rs200714678 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824324 | TGTTCACATTGGTAG[A/T]GAGTTTGCCTCAATT | 5521 |
rs200732565 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647220 | GTTTTTTGACGTTCA[C/G]TATTGCTTAGAAGCA | 5521 |
rs200735774 | in-del | -/T | 0.0444908 | 0.142359 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814225 | CCATATCCTATGGTC[-/T]TTTTTTTTTCTCTTT | 5521 |
rs200736277 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983199 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 5521 |
rs200758745 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751960 | CAGAAGAGTGGCAGG[A/G]AATGGGGGTAGGGAG | 5521 |
rs200769283 | in-del | -/A | 0.0232847 | 0.105357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813235 | CTTTTAATAATCATT[-/A]AAAAAAACCCCTCTC | 5521 |
rs200769633 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041171 | GGTTTTGGGTTAACC[A/G]CTCTGCAAGATGGTG | 5521 |
rs200774528 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687025 | GTAAGTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 5521 |
rs200776326 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708407 | TGTATGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 5521 |
rs200782664 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926398 | TATTTATTTATTTAC[-/T]TTTTTTTTGTTTTCG | 5521 |
rs200798572 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147017447 | TAACATTTGTTATCA[C/T]TAGAAAACAGAGTGG | 5521 |
rs200801935 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915475 | ACACACACACACACG[C/T]ACACATGTGTGCAAT | 5521 |
rs200812354 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966335 | TGTGTCCATCTTGTC[C/T]ACACTGATTTCAGCT | 5521 |
rs200814996 | in-del | -/CGCACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018042 | ACACATGCATGCGCG[-/CGCACACA]CACACACACACACAC | 5521 |
rs200820836 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909905 | TTAAGGACTACCCCT[A/G]TGGCTAATTTCTTTA | 5521 |
rs200834308 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689276 | TCATCATCCCCGTTA[C/T]ATAGATGAGACATTG | 5521 |
rs200834987 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868651 | TTCCACATAACTGCT[G/T]ACGATACTGCATTGC | 5521 |
rs200842988 | snp | A/C | 0.403334 | 0.197456 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013356 | ATCAAGCTACCAATG[A/C]CTTTCTTCACAGAAT | 5521 |
rs200846034 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590398 | TTGTTTTTTTTTTGT[G/T]TTTTTTTTTTTTTTT | 5521 |
rs200884068 | snp | C/T | 0.000247205 | 0.0111149 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698061 | TTCTATTTCTAAACT[C/T]TTCAGGTAATCGAAC | 5521 |
rs200885718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942138 | TTTCAGATTACATGC[A/G]CAAAGACTCTTTTCA | 5521 |
rs200888836 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684302 | CATATACCGAAAATT[-/A]AAACCTGGGGCAGTA | 5521 |
rs200902780 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146880968 | CCCAAAACCAAGGGG[-/A]AAAAAAGCTGTTGGC | 5521 |
rs200903778 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032191 | CAACGAACTCAAACA[A/T]ATCAGTAAGAAAAAA | 5521 |
rs200916579 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776724 | AACCCACAGAATAGG[-/A]AAAAAAATTTGCAAA | 5521 |
rs200927142 | in-del | -/AAAA | 0.45235 | 0.146814 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738396 | GTGAGACTCAGTCTC[-/AAAA]AAAAAAAAAAAAAAA | 5521 |
rs200931829 | snp | C/T | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864423 | AAAAAAAAAAAAAAA[C/T]CACAGCTTTCCGAAA | 5521 |
rs200931904 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786196 | ATAATAAATGGAAGG[-/A]AAAAAAAGAATCACT | 5521 |
rs200943583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727768 | AACTATAATCACCAA[A/G]TTGTGCAGATCTCTA | 5521 |
rs200960195 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936865 | ACCAGTGAGCCAGGG[-/T]TTTTTTTTTTTTTTT | 5521 |
rs200972834 | snp | A/G | 8.78789e-05 | 0.0066281 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697939 | GTATATAGTTTGGCC[A/G]ACTGTATCTCTGAAA | 5521 |
rs200974818 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934613 | AAAAAAAAAAAAAAA[C/T]AACGTGTTTGGTGCC | 5521 |
rs200983458 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846689 | TCTCAAAAAAAAAAA[A/T]TAATTTTATCTGTAT | 5521 |
rs200983478 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014221 | gaatggcaatcatta[A/G]aaagtcaggaaaaaa | 5521 |
rs201034186 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073636 | GTTTCCTTTAAATGC[A/C]CTCAAAACACCTTCA | 5521 |
rs201055877 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831186 | GCTTATAAAAAAAAA[-/A]GTTAACCTTTATTAA | 5521 |
rs201057281 | in-del | -/AA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893883 | CTTAAAGTAAAATTG[-/AA]AAAAAAAAAAAAAAA | 5521 |
rs201067055 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840228 | TTGAGTTCCCTTGAA[A/T]ATACATAACAAACAT | 5521 |
rs201071961 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976096 | TACCTAAAAGTTTCA[-/T]TTTTTAAAAAATTTA | 5521 |
rs201095701 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909786 | TTTAAGAGTCCCCAA[G/T]CTCTGGTTTCTAGGT | 5521 |
rs201103388 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781622 | AAGAAAAAAAAAAAA[-/A]GAGACAAAATTTTAG | 5521 |
rs201104147 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828048 | GAGACAGAGACAGAC[A/G]ATCATGTACGCTTTC | 5521 |
rs201108252 | in-del | -/TCC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002565 | TCCGATTTTTCTCGG[-/TCC]TCTTCTTTGTGGTCT | 5521 |
rs201124013 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693264 | CTGTCACCTAGGCTG[-/G]AGTGCATTGGCGAGA | 5521 |
rs201125456 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632073 | TGTGCCCCCCCCCCC[C/G]CCCATTCATATATTG | 5521 |
rs201138386 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733892 | CAGTAGTAGTGGTGG[G/T]GGTAGTAATAGTAGA | 5521 |
rs201139552 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750095 | AACAAACAAACAAAC[A/T]GAGTTGAACATATTT | 5521 |
rs201140438 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756960 | AGGAGGCAGACAAAT[A/G]AAGATTAAGGAGGGT | 5521 |
rs201141603 | in-del | -/ACAT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866644 | CATATATATACACAC[-/ACAT]ATATATGCACACAGA | 5521 |
rs201148779 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735578 | TAAATTGGATGGGGG[-/A]AAAAAAGAGTCTCAC | 5521 |
rs201157623 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679344 | CTGGCTAGCCATATG[C/T]AGAAAGCTGAAACTG | 5521 |
rs201163891 | in-del | -/TGTGTGTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708400 | ATATCTATGTATGTG[-/TGTGTGTA]TGTGTGTGTGTGTGT | 5521 |
rs201190200 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970438 | AACCCCATCTCTACT[-/A]AAAAAAAATTAGCCA | 5521 |
rs201223325 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007889 | AACTGTAACACTCAC[C/T]GTGAGGGTCCGCGGC | 5521 |
rs201225513 | in-del | -/ATATATATATATATATATATATATATATAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772384 | GTTAATAACTTGTGC[lengthTooLong]ATATATATATATATA | 5521 |
rs201276212 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027265 | TGTGGTTATACAACA[A/T]TGCAAATGTACTAAA | 5521 |
rs201287081 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052350 | TAAGCACCTATAATG[G/T]GCCTGGTATTGTTCT | 5521 |
rs201288268 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635972 | TAATGTCACTTATAA[C/T]ACCCATAGTTATTTT | 5521 |
rs201288645 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915847 | CCAAGACAAAAAAAA[-/T]CAATTTCAACACTGT | 5521 |
rs201298747 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003536 | AGATCAAACCCTGGC[A/C]TTTAATGAAAAGAAT | 5521 |
rs201299020 | in-del | -/ACAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009865 | TATACACACACACAT[-/ACAC]ACACACACACACACA | 5521 |
rs201301079 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933395 | CTTAATTATTTCTTT[-/A]AAAAAATCAAAAGAT | 5521 |
rs201325698 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647218 | ATGTTTTTTGACGTT[A/C]ACTATTGCTTAGAAG | 5521 |
rs201352923 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004274 | ATCACTAGAAGACAC[-/A]CTGCCCCAGAGGGCA | 5521 |
rs201356555 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734063 | TGAGTTAGGTTTTTT[G/T]TTTTTTTTTGAGACA | 5521 |
rs201376705 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014419 | ATAAATCATGCTGCT[A/C]TAAAGACACATGCAC | 5521 |
rs201383522 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079471 | ATATATATATATATA[C/T]ATGTGCAATGGAATA | 5521 |
rs201397586 | in-del | -/AGAGAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745203 | GAGAGAGAGAGAGAG[-/AGAGAA]AGAGACTATAAGCAT | 5521 |
rs201401015 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878107 | TGGGAACCAGAAGCC[A/C/G]GCAGACAAGTATCCA | 5521 |
rs201416919 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615513 | ATAATAAAAAAAAAA[A/T]TTAAAAAAAAAAAAA | 5521 |
rs201430774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936971 | TCGAACTAGACAGTA[C/T]AAAATTCCATTTGTG | 5521 |
rs201448902 | in-del | -/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734057 | ATAAAATGAGTTAGG[-/TT]TTTTTTTTTTTTTTG | 5521 |
rs201454891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736591 | ATCATAGCAGCCATC[A/G]TAAGTCTTGAGGACA | 5521 |
rs201455654 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677045 | ACTCCTGAACTCCTA[C/T]CTTTGTTGTCTGCTT | 5521 |
rs201458594 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078746 | CCAGGAGGCAGAGCT[C/T]GCAGTGAGCCGAGAT | 5521 |
rs201461777 | snp | C/T | 1.65337e-05 | 0.00287517 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650661 | TGTGATATGTGTGTG[C/T]GTTGGCAAATACTCT | 5521 |
rs201464410 | snp | A/G | 0.176219 | 0.238865 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626140 | GTTTTAAGCCACTAC[A/G]TTTGTGAGAATTTGT | 5521 |
rs201475672 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077114 | AATATATAATATGTA[-/T]ATATTGTATATTGTA | 5521 |
rs201476258 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981062 | TGTATTTCTTACTCA[-/T]TTTTTTTTTGTTTGT | 5521 |
rs201476830 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016360 | GATGATAGCAGTTTT[-/G]GGGGGGGACAATCAT | 5521 |
rs201486029 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678855 | TGTGAAGGACCTCTT[C/G]AAGGAGAACTACAAA | 5521 |
rs201489833 | in-del | -/CTGT | 0.028044 | 0.115046 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590263 | AATGACATATCTTCA[-/CTGT]CTGTCTTTTCTTTTT | 5521 |
rs201493206 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146613176 | GGGCTTCATCCCTGG[C/G]ATGCAAGGCTGGTTC | 5521 |
rs201515041 | snp | A/G | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918471 | AGGCTAAGCATTTGT[A/G]AATATTATTTTATTC | 5521 |
rs201521141 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948583 | GTAGAAAACAAAGGG[A/G]AAAAAAGAAATAACT | 5521 |
rs201525035 | in-del | -/TA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077136 | ATATTGTATATGTAT[-/TA]TATATGTATAATATT | 5521 |
rs201554442 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856480 | CAAGAAGAGTAGGTA[C/T]AAATAATAATACGAA | 5521 |
rs201580774 | in-del | -/TTTTTATTTTCTT | 0.0142736 | 0.0832652 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881393 | TCACTAGATCTTTTA[-/TTTTTATTTTCTT]TTTTTATTTTATTTA | 5521 |
rs201593853 | snp | A/C | 3.35762e-05 | 0.00409719 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698132 | CACCCCTACGATGAA[A/C]CTGATTTTTACTCTG | 5521 |
rs201604909 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984030 | TGAACACAATATAGA[A/G]CAATTAAATCAAATT | 5521 |
rs201612378 | in-del | -/AATTAAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712860 | TCAAGATTTAGGGTT[-/AATTAAT]TCATTCATTGACCCA | 5521 |
rs201618886 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652769 | GGCAACACCCCCCCC[A/C]AAAAAGTTTTGCCAT | 5521 |
rs201624064 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933928 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTTTG | 5521 |
rs201626725 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626391 | TGGCACCACAAATGG[-/A]AAAATGGTCATAAAA | 5521 |
rs201627842 | in-del | -/GGAAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063076 | AGAAGAGAAGGGAAA[-/GGAAG]GGAAGGGAAGGGAAG | 5521 |
rs201630334 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039969 | AATGAAACATTTATT[A/G]AGTCCCTTCTAAGCC | 5521 |
rs201638638 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863470 | TACCCTTGGCTCCAA[A/G]ACAGAAGAGGAAGAG | 5521 |
rs201639838 | in-del | -/TTG | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918209 | GCAAGGCAGAGAAGC[-/TTG]AAAGAAACAGGAGGA | 5521 |
rs201656527 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908418 | TACTTAAAAATTAAA[-/T]TTTTTTTTCTTTCAA | 5521 |
rs201658038 | in-del | -/T | 0.419936 | 0.183362 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824739 | TGCAAGAATCAATAC[-/T]TTTTTTTTTTTTTTT | 5521 |
rs201660654 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012395 | TATTCTCTGATGGTA[A/G]TTTGTATTTCTGTGG | 5521 |
rs201662558 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862871 | TGGAAAAAAAAAAAA[-/C]AAAAAACCCTGGCTT | 5521 |
rs201664006 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617787 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 5521 |
rs201677143 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724033 | TATATTTAGGACAGT[A/G]CCTGGTACAATGGTA | 5521 |
rs201688271 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911091 | GTTAGACACTTTCTT[G/T]TTTTTTTTTTGAGAT | 5521 |
rs201706230 | snp | C/G/T | 4.95277e-05 | 0.00497612 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589974 | GTCCTGGAATATATA[C/G/T]AGGTTATTTGTAGCC | 5521 |
rs201709204 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708413 | TGTGTGTGTATGTGT[A/G]TGTGTGTGTGTGTGT | 5521 |
rs201722283 | snp | C/T | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590192 | TTCTGTCGAACATCC[C/T]GAAGAAGTTGTTGTA | 5521 |
rs201750288 | in-del | -/TGTATAGG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637397 | CTAAACATCCTACAA[-/TGTATAGG]ACAGCCCCTTCCCCG | 5521 |
rs201769200 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016595 | TTGTGGAATCAATAT[A/G]TGTAGTGAGGAAAAT | 5521 |
rs201780722 | in-del | -/AT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075948 | TGTTGTTTAAAATAT[-/AT]TTCTAATTATATTAT | 5521 |
rs201784412 | in-del | -/GGC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644316 | ATTGTTTTTGGCTTT[-/GGC]TTTTAAAATTTCTTT | 5521 |
rs201836451 | snp | C/T | 0.000115452 | 0.00759687 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589989 | TAGGTTATTTGTAGC[C/T]GCCACTGCTATAATA | 5521 |
rs201848951 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003571 | CTTTAGCTGCAGCCC[A/T]AGAGTTTGGAGATAC | 5521 |
rs201850358 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032187 | TCTACAACGAACTCA[A/G]ACAAATCAGTAAGAA | 5521 |
rs201867657 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927064 | TTGGCAGAACCTATA[-/G]GCTGGGTTGAGGTGG | 5521 |
rs201880757 | snp | C/G | 3.33584e-05 | 0.00408388 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698122 | ACATTGTATTCACCC[C/G]TACGATGAACCTGAT | 5521 |
rs201884670 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680413 | GGTGGGGTGGGGAGG[G/T]AGGGATAGCATTGGG | 5521 |
rs201895729 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978509 | TGATTTTACGTACTA[C/T]GTTTAAGTCTTTAAT | 5521 |
rs201901026 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755771 | TTAGGCTTGTGCTAA[-/T]TTGTTTTTCAACTTC | 5521 |
rs201906490 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898789 | ACAAGAAAAAAACAA[A/C]CAACCCCATCAAAAA | 5521 |
rs201921319 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720488 | TGGTTAATCTAAAAT[A/G]TATCATATGGACCAT | 5521 |
rs201925565 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915476 | CACACACACACACGT[A/G]CACATGTGTGCAATT | 5521 |
rs201942886 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936882 | TTTTTTTTTTTTTTT[A/G]TTCAATGCTGTCTAA | 5521 |
rs201977073 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943675 | TTAGAGAGGCACTCA[-/T]TTTTTTTTTTTATAG | 5521 |
rs201984103 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659047 | AGAAATGATCAAAAA[A/C]CTTTTAACATGATTT | 5521 |
rs202005549 | in-del | -/CGCGCACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667329 | AGGAATAGGCGTGCG[-/CGCGCACA]CACACACACACACAC | 5521 |
rs202021652 | snp | A/C | 0.00199802 | 0.0315439 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590242 | CTGCAAGGCAGAGAG[A/C]AAAGGCAATGACATA | 5521 |
rs202038761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055622 | GTCAGACACCAGCCC[A/G]CTTTTCCCACCCACC | 5521 |
rs202038997 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049125 | GTGTGTGTGTGTGTG[A/T]GATATTTTACATAGG | 5521 |
rs202045492 | in-del | -/C | 0.0178098 | 0.0926698 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814714 | CATTGCACATGTGGT[-/C]CCCCCCAAGTGCTGG | 5521 |
rs202060447 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937303 | GAGACTCCGTCTCAG[-/A]AAAAAAAAAAAAGGG | 5521 |
rs202070784 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589923 | TATTCAGTATGTGAG[A/G]TTATTAAGTAATAAC | 5521 |
rs202071450 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822552 | TTTTTTTTTTTTTTT[A/C]CTTTTTAGGTTGTCC | 5521 |
rs202077198 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708408 | GTATGTGTGTGTGTA[-/TG]TGTGTGTGTGTGTGT | 5521 |
rs202100048 | in-del | -/AATATAAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027288 | TACTAAATACCACTG[-/AATATAAC]CATTGTTCATCTGAA | 5521 |
rs202109053 | in-del | -/ATATATATATATATATATATATAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772384 | GTTAATAACTTGTGC[-/ATATATATATATATATATATATAT]ATATATATATATATA | 5521 |
rs202136792 | in-del | -/CA | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715927 | CTTTTCCATCATTGT[-/CA]CACACTCCATCAAAG | 5521 |
rs202143511 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840244 | ATACATAACAAACAT[G/T]TAATTGAGTGACTCC | 5521 |
rs202154889 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988909 | ATAAAAACAGAAATG[-/A]AAAAGATGACATTAT | 5521 |
rs202165306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828683 | TCCCCCCAACACAAA[A/G]CAGACAACACTAAAA | 5521 |
rs202165505 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146614465 | TCATGTCCAAAACAC[C/T]AAAAGCAATGGCAAC | 5521 |
rs202170847 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146679030 | CCTTTCTTCACAGAA[C/T]TGGAAAAAACTACTT | 5521 |
rs202181881 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077707 | CCATGCCAGTGGCTG[G/T]GTGTTTGTGACCAAC | 5521 |
rs202185784 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950436 | CAAAATTATGTCACA[-/T]TTTTTAAAAAAAATT | 5521 |
rs202214722 | in-del | -/TTAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848136 | TATGTTTCTTATTCT[-/TTAG]TTTTTTTTATCTTAT | 5521 |
rs202230823 | snp | A/G | 0.00299541 | 0.0385841 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589931 | ATGTGAGATTATTAA[A/G]TAATAACTTGTCCAC | 5521 |
rs202232647 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024204 | ATCTATCTATCTATC[A/T]CCTACTGGTTCTGTT | 5521 |
rs202238841 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032207 | ATCAGTAAGAAAAAA[A/G]CAAACAATCCCATCA | 5521 |
rs207466448 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785426 | GGTAGTGCACACCTG[C/T]AATCCCTGGTACTTG | 5521 |
rs267600473 | snp | A/G | | | intron-variant, missense | PPP2R2B | GRCh38.p7 | 5:147055734 | GCAGGTAACGAGAGA[A/G]GCATTTCATCTTCCA | 5521 |
rs367550088 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934016 | GGACATGAACTCATC[A/G]TTTTTTATGGCTGCA | 5521 |
rs367556730 | snp | A/T | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919315 | GGGAGGTGATCTTTT[A/T]CCCAACTAATTTCAG | 5521 |
rs367570704 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728676 | GAGTTAATTGAATCA[C/T]GGGGACTGGTCTTTC | 5521 |
rs367572964 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959413 | ATTGTAGTATAGGTA[-/A]TCAAGTGCTATGATT | 5521 |
rs367576942 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736059 | TAATTGAATCATGGG[A/C]GCAGTTTCCCCCATC | 5521 |
rs367585192 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618147 | CCTTAAGACAGATTA[C/T]GTTAGATTATCTGAG | 5521 |
rs367587994 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797681 | ATTTATTGAACATGC[A/G]GTAACTGTCTGGTGA | 5521 |
rs367590820 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064515 | TACGGCCTCAGAGAC[A/C]TGGGCTGTGATAATG | 5521 |
rs367591435 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598276 | GCAGTTGATGACTTA[C/T]TTTTCCTTAAGACAG | 5521 |
rs367592959 | snp | C/T | 6.98434e-05 | 0.00590904 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697956 | CTGTATCTCTGAAAA[C/T]ACCAAACAGGAATTC | 5521 |
rs367598517 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032525 | TCTCCCTCTTTCCCC[-/C]GAGTCCCCAAAGTCC | 5521 |
rs367602463 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768511 | TCACTGTCCACTGTC[A/T]TGGCCTCCAAATCTG | 5521 |
rs367604524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846358 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 5521 |
rs367609820 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645625 | AAGCCAAGAGTTGAG[A/G]CTACCTGGTCCCTTA | 5521 |
rs367619550 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791624 | CAAAGCTCTCCAAAC[-/A]TGTCAAACATTTTCA | 5521 |
rs367623865 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882046 | ACTTTGGGAGGCTGA[C/G]TCAGGCAGATTATGA | 5521 |
rs367625131 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603763 | ATTTAGTTGTTAAAA[-/C]CAGCCTATGAAGTAG | 5521 |
rs367636310 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810241 | AAAGAGGCTTAATGG[A/G]CTCACAGTTCCATGT | 5521 |
rs367644964 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598292 | TTTTCCTTAAGACAG[C/T]TTCTCTATTTGGCTT | 5521 |
rs367655244 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877523 | TTTTGGGGTTTTGAT[G/T]GTCTAAGCAGGTAAC | 5521 |
rs367669997 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893103 | TCTTTCCTGTCACTC[A/T]TCCATCCATTTATTC | 5521 |
rs367673704 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869113 | GGTTTTGGAAGACAC[A/G]GTACTGGGCACATAT | 5521 |
rs367684210 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965215 | AAAATATATAAGATG[A/G]AAATTTAAGCCATAT | 5521 |
rs367685182 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608716 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 5521 |
rs367697787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885263 | AAAGTCAGATAGATG[A/G]GAGCCTGGCGCCAAC | 5521 |
rs367706024 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974978 | ACAGGCGTGAACCAC[C/T]GTGCCCCGCCTATTT | 5521 |
rs367708610 | snp | C/T | 6.75026e-05 | 0.00580919 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650733 | CAGGCACCTGGGATG[C/T]AAGAGAAACAAATCA | 5521 |
rs367725708 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792623 | GGGACTTCAATTTCA[A/G]ATAGGTACTCAAGAA | 5521 |
rs367730118 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843175 | CTGGGCAATGAGGGC[A/G]AAACTCTGCCTCAAA | 5521 |
rs367746413 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886096 | GTAGCCCCAACACTT[C/T]GGGAGGCCGAGGCGG | 5521 |
rs367760694 | snp | C/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922508 | CATCTCCTCCCAGCT[C/G]TCTTCAACATCCTAG | 5521 |
rs367776274 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663897 | ATCCAGGATGGAGTA[C/T]AGTGGCATGATCTTG | 5521 |
rs367788638 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027462 | ACATGGTGACACCTC[A/G]TCTCTACTAAAAATA | 5521 |
rs367794238 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940272 | GCTGCAGATTCAGGC[C/G]TGGATGATTGAAGCG | 5521 |
rs367797913 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990848 | TATATAAGAAACTCA[A/G]TGATTCAATAGCAAA | 5521 |
rs367798804 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688969 | CTTATTCCCAATATA[C/T]TGCCAGTACGGTGTT | 5521 |
rs367801338 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877941 | CCAGCTGCCCAGGAA[A/G]CACAGTGATCCGCAA | 5521 |
rs367807664 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976123 | TTTATTATTATTATT[A/G]TTATTATTATTATTA | 5521 |
rs367808400 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909958 | TCCATTTATCTAATT[G/T]CAGCTAGAAGATTTA | 5521 |
rs367809667 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986238 | GAGAAAAGTGTGTGT[C/G]AGACTTTGCATTGGA | 5521 |
rs367822326 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656472 | CGATCCCACTACTGA[G/T]CAATACGGGAGTTTT | 5521 |
rs367822857 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708679 | AGTGTCTCTATTGAT[A/G]TGACTCAACTTGATT | 5521 |
rs367823295 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812432 | AGGATAATAGCACTA[C/T]TACTTTCCCAGGCCT | 5521 |
rs367831804 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697764 | ATGGGTCTCACATAA[C/T]TGGGTCATAAATTTA | 5521 |
rs367832882 | snp | A/G | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923898 | TGCAGCCACAGGAAA[A/G]AAGAAATGGTAGTTT | 5521 |
rs367847299 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733007 | ACTGATACACACTCA[C/T]GGCAAAAATTATTTT | 5521 |
rs367870534 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785973 | TTCGATAGCACAGTA[A/G]GGTGACTACAGTTAT | 5521 |
rs367879893 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773377 | CTTTTCAAAAGGCTT[A/G]CACAAAGCAGAGCCA | 5521 |
rs367882183 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804024 | TAAAAAAAATTAGAC[C/G]GGCGTGGTGGCCAGT | 5521 |
rs367891860 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589622 | ACAACCTCATTTTAT[C/T]GCAGCAGACACCTAG | 5521 |
rs367892865 | in-del | -/AAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943106 | CCGGCCCAAATCCAT[-/AAT]TTTAATCTAGTATTT | 5521 |
rs367894876 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782863 | AGAGACAGAGAGAAA[-/CA]GAGGGGGAAGGAAGG | 5521 |
rs367901780 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703509 | GCCTTACAATGAGAA[C/T]TAAAGATGGGCCTTT | 5521 |
rs367903080 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792491 | CTTTTGGAACACAGA[C/T]TCTGGTGGAGGGAGA | 5521 |
rs367928507 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782672 | TTGCCCATTTTTTTT[-/T]AAAGAGTTGATCCAT | 5521 |
rs367933099 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850109 | TTATGTCTGGGTAAG[C/T]GTGTGTGGGTGACAC | 5521 |
rs367950486 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798255 | GTTTTTCATCTTCCA[A/G]GGAGACTTACCCTCT | 5521 |
rs367950756 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900591 | TTCCTTCCTTCCTTC[C/T]TTCTTTCCTTCTTTT | 5521 |
rs367952030 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615294 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGATCA | 5521 |
rs367963080 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977307 | AAGCATAGTTCACTG[C/T]AGTCTTGAACTCCTG | 5521 |
rs367965573 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749710 | TTCACGCCATTGTCC[A/T]GCCTCAGCCTCCCGA | 5521 |
rs367974709 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811722 | CCCACCACCACGCCC[A/G]GCTAATTTTTTTTTT | 5521 |
rs367984750 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680177 | TAGACTGGATTAAGA[A/T]AATGTGGCACATATA | 5521 |
rs367989664 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660094 | ATAGCTCCGTCCTCA[C/T]TGTCATGAAAATCTT | 5521 |
rs367994015 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035128 | GTATAAATAACTGCC[C/T]GAGACTGGGTAAATT | 5521 |
rs368000533 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607934 | TGAGCATGTATCCCA[A/C]ATGAAGGCTTTGCAT | 5521 |
rs368006187 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943076 | TGCTGGGATTACAGG[C/T]GTGAACTACTACGCC | 5521 |
rs368008366 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013874 | GGCAACGAAAGCCAA[A/G]ATTGACAAATGGGAT | 5521 |
rs368017944 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046512 | CAATGATTTCACTGC[C/T]GGTGATTTTTCTATT | 5521 |
rs368020209 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956933 | GATTCTATCTTCATG[A/G]CCTCATCACCTCCCA | 5521 |
rs368021236 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146698039 | ATCTTATTTTATTGA[C/T]TTTTTCTTCTATTTC | 5521 |
rs368021752 | snp | A/C | | | stop-gained, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650616 | CGGACATGTAGGTTT[A/C]ATAGTCGCTGTTGAC | 5521 |
rs368022594 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651172 | CATCTCATGGCTTTG[G/T]AAGCTATACCCCTTC | 5521 |
rs368026214 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640501 | CTTTATGGCCATGAC[A/G]TGGCGTTGGGTAAAC | 5521 |
rs368064153 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651713 | AAATAACCAAAGCTA[C/T]TTTCTTTTCAAGCAA | 5521 |
rs368070692 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925707 | TTTTGGAAGTTTTGG[A/C]CATTATTTTTTCAAA | 5521 |
rs368081191 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822551 | TTTTTTTTTTTTTTT[-/T]GCTTTTTAGGTTGTC | 5521 |
rs368085686 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020622 | AGTGCTTGAAAAGTT[A/G]CTTGACTGTATCTTT | 5521 |
rs368087475 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749302 | TAACTAGTCTTTGTC[C/T]GACATGTGGTTTTCA | 5521 |
rs368105052 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984696 | TTCCACCAGCAGTGT[A/G]CAAGGGTTCCTGTTT | 5521 |
rs368111278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900209 | ACAAGATCCACTAAT[A/G]GGTCGACCCAAGGAA | 5521 |
rs368112602 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896970 | CTCCTTGATTTAGAA[C/T]AAGCAGAAAAAGAAA | 5521 |
rs368119736 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688575 | TAAGAAAGCAAGAAC[A/C]AGAGTTGGAATTTTC | 5521 |
rs368122883 | snp | A/C | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916724 | AATCTGTAGACTATG[A/C]CAGAATAGCAACTCT | 5521 |
rs368127573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728928 | GAAAACAGACTAATA[C/T]AGCAAATTGGTACCA | 5521 |
rs368135841 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082065 | TTCAAGAGAATATTG[C/G]AGAATCAAATTTTGG | 5521 |
rs368140091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058166 | GGTGAGTAAGTGAAT[C/T]GATGAATGGATAAAT | 5521 |
rs368164267 | snp | A/C/T | 6.9029e-05 | 0.00587456 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650758 | AAATCACTTCAGAAC[A/C/T]AAAGATCTTCCATAG | 5521 |
rs368181799 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689831 | CTCCAGAGCTGAAAG[C/T]ATAGGCTGATCAGAG | 5521 |
rs368187039 | in-del | -/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885335 | TTTGAGCTATTGTGA[-/GT]GTGTGTGTGTGTCTA | 5521 |
rs368204750 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615122 | GTCCAACAATGATAG[A/G]CTGGATTAAGAAAAT | 5521 |
rs368205515 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749153 | CATTTCCTTAATGGC[C/T]GATAGTGTTAAACAT | 5521 |
rs368210959 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595397 | ATCTGTCACCATTCA[C/T]CTTCGGCATTTTGTC | 5521 |
rs368211962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726270 | ACTAGGATTTTGGCC[A/G]ATTTAAGCCAACTAG | 5521 |
rs368224837 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673635 | AAGGAAGATTCAAAA[A/C]TAAGACCCTTGACTT | 5521 |
rs368236266 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060640 | CTGTCTTAAAAAAAA[A/G]AAACAACAAAAAAAC | 5521 |
rs368246421 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062345 | TCAAGTGATGCATGA[C/T]GGTAGTAGTAATAAG | 5521 |
rs368248054 | in-del | -/TAAAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851660 | CTCACTTTCTCAAAT[-/TAAAT]AAGTGTAGGCAAAAC | 5521 |
rs368259580 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016752 | AAGAAGGCAAGAGAA[C/T]GGGCATTCTATCCAG | 5521 |
rs368260233 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998113 | TCCCTCTTCACTTTA[C/T]ATACCCCATACAAAG | 5521 |
rs368280685 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739458 | GAATGCCAGGGGTGG[A/G]GGACAACTCATATGA | 5521 |
rs368285537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026143 | ACTCCAGAGGGAAAA[A/T]GGATAGATCTCCATA | 5521 |
rs368288350 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821015 | CTAATAGGCCTCCCT[C/T]CTTCCATCATTCCGC | 5521 |
rs368288770 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769222 | TCTCGATGTTACTCC[C/T]TATCACAGTAGTTTT | 5521 |
rs368297738 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813618 | TTCTTAGCATCAATA[A/C]AACACCTCCTTTTTA | 5521 |
rs368298472 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877832 | GAGCTCGCCTCGCGG[A/T]GCCCGGATGGATGCG | 5521 |
rs368304793 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803275 | CAGTGCTGCCTGAAA[A/C]CCGACATTAGAACTA | 5521 |
rs368305889 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888120 | CACTGCTGTGACCTC[C/T]AAATGTATAACTACC | 5521 |
rs368308111 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848469 | AGACTTACCTTACCT[C/T]TGATGATCTTGACAG | 5521 |
rs368313981 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864811 | TTTTCTCTGATCTTC[A/C]CCCCACATAAGTTTC | 5521 |
rs368317175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915997 | CGGACTTGTAAGACA[C/T]GTGACTTTCACTTTG | 5521 |
rs368352797 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961487 | ATTCTAACTTTTGCC[A/T]ACCTGATAGGTAAAA | 5521 |
rs368355672 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642253 | AAAATAATAATTGAA[C/G]ACACCAGGAGGTCAC | 5521 |
rs368365132 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824774 | TGGGGCTGAAGTGCA[G/T]TGGTGCAATCTCGGC | 5521 |
rs368368289 | snp | C/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866787 | AGCACTCAGTATATA[C/G]TGGCTCTTCCTCATG | 5521 |
rs368371033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907405 | TGTTCCCATATGAGC[A/G]TTCCCAAAGTTCAGC | 5521 |
rs368374553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843199 | CCTCAAAAAAACTTT[A/G]AAATTATCCAGATGC | 5521 |
rs368379969 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899560 | AGCACACCAGCATGG[A/C]ACATGTATACATATG | 5521 |
rs368382561 | in-del | -/AATT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668191 | CTAAAGAAAACGATT[-/AATT]CTCTAGCTTCCTTCT | 5521 |
rs368387300 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830329 | CACAAGCTAATGCCT[A/G]TAAAAAACTAGCTGT | 5521 |
rs368387966 | in-del | -/CT | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921726 | TGTATCAGTTCATCT[-/CT]GTTTCTCTTCTGACA | 5521 |
rs368394110 | in-del | -/TTTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983177 | TGTTTTCCAGAGCAT[-/TTTTT]TTTTTTTTTTTTTTT | 5521 |
rs368399583 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029317 | ATCTGAAATTGCTTT[A/G]TGTGCCTGTGGTAGG | 5521 |
rs368400270 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075536 | ACTCATATATATACA[C/T]ACAACTTCCTTCTTG | 5521 |
rs368416804 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146910901 | ATATCCCACTGGTCT[G/T]CCTTTGGGTTCTTAA | 5521 |
rs368420743 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701962 | CTATGATTGGATTTA[C/T]TAGGGCTATTTTTAG | 5521 |
rs368425718 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725196 | AAAACAGTTTCCATG[A/G]TGATTCTTCTTTTGA | 5521 |
rs368441501 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743272 | CTTCCCTTTTCACCA[C/T]TCAAATAGGATTTTT | 5521 |
rs368442816 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697123 | ATTAAAATGTATATT[-/T]CCTCATAGACTCACA | 5521 |
rs368445996 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822755 | TTCTTTATGACCAAC[A/G]CATGAAACAGTGATT | 5521 |
rs368447238 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711567 | CAGGAAGAGAAAGCA[A/G]ATGGGTTGGGGGAGA | 5521 |
rs368450326 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797015 | AAATCAGCTAAACTC[G/T]TCCAAAAGTTTTGGG | 5521 |
rs368451804 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863133 | CAGAGAACCTACAGA[A/G]AAATACATCTTGTTC | 5521 |
rs368457166 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856309 | AAACTATGCTTCCTA[C/T]GTACAATAACTATTT | 5521 |
rs368457702 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773197 | CAGCGTAAGGGATTA[A/C]ACAGTATTATCCAGC | 5521 |
rs368468958 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833388 | CACTAGTCACAGCAA[A/G]AGTACATGCAAGGAT | 5521 |
rs368471423 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826014 | TAAGAAGAATTTCAC[C/T]TGAAAGAAAGTAGAG | 5521 |
rs368507145 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810523 | GACACAGCCAAACCA[C/T]ACCAGATGCGGAAAC | 5521 |
rs368509769 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788018 | TCTCATGTCTGCTTT[C/T]GGAGGCAAAGTCAAA | 5521 |
rs368510943 | snp | A/G | 4.94344e-05 | 0.00497139 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593065 | GGTAGTCATGAACCT[A/G]GAGAGGAAACATATC | 5521 |
rs368519002 | snp | A/G | 0.000362863 | 0.0134648 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638357 | ATGGGGGTGGAACTC[A/G]GCTGCTGTGATCACC | 5521 |
rs368528915 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917184 | GGCAAAAGCAAGCTG[C/T]ATCATAGTTGCTCCT | 5521 |
rs368551088 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698319 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 5521 |
rs368553019 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829664 | AGCAAAACTGACTTA[C/T]GTAAAAGAGGCGCAG | 5521 |
rs368563037 | in-del | -/GAGA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051321 | TGGCGTTTAATAAGA[-/GAGA]CTGTTGTGAGGAGTG | 5521 |
rs368567829 | snp | C/T | 0.000171101 | 0.00924777 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856613 | GGGTTCAGATCCAGA[C/T]TCCAGGAGGTAGTGA | 5521 |
rs368578559 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034573 | TATTTTTTCTTTACT[C/T]AAAGGGAAATAAGTA | 5521 |
rs368580221 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937677 | GAGTGAGCCGCAGTT[A/C]CACCTTCACGGAGGC | 5521 |
rs368587212 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922655 | AGCATTCTCCCACTA[C/T]CCTGGTAACAGTACC | 5521 |
rs368592151 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909446 | ATGTTACTACCCTCT[A/T]AAGAGGTCAGTAAAG | 5521 |
rs368601208 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041731 | AGATCTTCATTTTCT[C/T]TATTTTTATTATTTG | 5521 |
rs368610872 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928020 | GCTGGGATTACAGGC[C/G]TGAGCCACCACACCT | 5521 |
rs368615300 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972482 | TTTGGGAGGCTGAGG[C/T]GGGTGGATCACCTGA | 5521 |
rs368617332 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671216 | AATGATATACACCAA[G/T]GTAGTATGTTAGGTG | 5521 |
rs368624770 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949595 | GTACAACCACTAGGT[A/G]GAACAGTATGTAGAT | 5521 |
rs368629830 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927837 | CTCCTGGGTTCAAGC[G/T]ATTCTCCTGCCTACT | 5521 |
rs368632254 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746394 | AGTTTAAAAAAAAAA[A/G]GTCATATGTAGCAAT | 5521 |
rs368632718 | in-del | -/AC | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865293 | CTCTCTTTGTCTCTG[-/AC]ACACACACACACACA | 5521 |
rs368635271 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615381 | GGGGGAGGGATAGCA[C/T]TGGGAGATATACCTA | 5521 |
rs368639892 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635861 | GACCAAGTCAGATTC[A/G]GTTCTTATCCTCAAG | 5521 |
rs368647447 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621169 | TGGATCAGGCAGTCT[C/G]CCTCTGTGTTCCCAG | 5521 |
rs368653680 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987224 | TAAAGACCTCATTAC[C/T]ACCAGACCTGACTTA | 5521 |
rs368665194 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009550 | TGAGGTGGAAGGAAA[G/T]ATTAAGTTTGCTGGC | 5521 |
rs368683396 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787064 | ATGTGGATCTTTAGT[A/T]GCAGATGTGGGATTT | 5521 |
rs368688490 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719413 | CATCTCTGTCATTTA[C/T]AAGTGATGTGCCTTT | 5521 |
rs368700846 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014496 | CAACACAAATGTCCA[A/T]CAATGATAGACTGGA | 5521 |
rs368708084 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951793 | GATTCCATGTGTTTG[C/T]TATTGTGAATAGTGT | 5521 |
rs368710241 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723723 | TTTCTAAAACACACG[C/G]CCTGATCTTCTAACA | 5521 |
rs368725040 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813271 | ACACAAACACACATA[A/C]CTCACATACCAATTC | 5521 |
rs368737531 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909292 | ACTTATCAGTAAGTA[C/G]AGCAGTTCTTGAATT | 5521 |
rs368740693 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057930 | AGTTCATATAAAGGG[C/T]TTAGCTCAGTGTCTA | 5521 |
rs368752413 | snp | G/T | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082635 | TACATAAATCATGGG[G/T]AGGGCATTATTATCA | 5521 |
rs368759319 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988205 | CTTCAGCAATGAACA[A/C]ATCATCTAGACCAAA | 5521 |
rs368761556 | in-del | -/ATAGCTAAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901101 | TTTTCTTATGTAAAC[-/ATAGCTAAA]GATATTTTACAAATT | 5521 |
rs368763869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950055 | CAGTATTTGATAGCA[C/T]AACAGAATGATTACT | 5521 |
rs368787138 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600498 | GACAAATTTAGCAAT[C/T]CTTATCAACTGACTC | 5521 |
rs368804349 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662678 | GACTAAGACTATGGG[C/T]TTAAAATGATTTTTA | 5521 |
rs368805657 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847895 | GGATACGAGCTCCTG[A/C]GGCTTGGCTTGGCAG | 5521 |
rs368808686 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639019 | TAATCCTTACAAGAA[C/T]TCTATATAATTAGCG | 5521 |
rs368816711 | in-del | -/C | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861814 | ACATACCCTTTTTAT[-/C]ATGGATGAAGCTACC | 5521 |
rs368838897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057454 | CAGCAGTGAGGGAGT[A/G]GAAGGAGTGTGGGCT | 5521 |
rs368857856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844261 | TAATGCTAGATGACA[C/T]GTTAGTGGGTGCAGC | 5521 |
rs368861823 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936471 | TTGTAAGCAGGAAAA[A/G]AAAAAAAAAAAAAAC | 5521 |
rs368861887 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654450 | TGAAATATCAGCAAT[A/C]TCATGCGGTTTAACC | 5521 |
rs368872043 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969577 | GACAAGGCTATACCC[A/G]GGATGCCACAGCCAT | 5521 |
rs368877822 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880421 | GCTGTATCTATCACC[A/G]AGGTTCCAACATTCA | 5521 |
rs368881641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997729 | AAATTTTTAGAATGG[A/G]TAGAATTTAATTTTT | 5521 |
rs368903122 | in-del | -/A/AA | 0.493969 | 0.05458 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741035 | GCAAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 5521 |
rs368904348 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713461 | GTAAAGCTTATGTTA[C/T]GTACATTTTACAACA | 5521 |
rs368905594 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634981 | AGAGGGTTGGGGTTT[C/T]GAACATCTTATGTCT | 5521 |
rs368909810 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872475 | CATATGACACTACCC[C/T]CTTTTATTTTTTCAA | 5521 |
rs368918751 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619611 | CTAATTTTTTCATGT[C/T]AGCAACTAACTAAAG | 5521 |
rs368926347 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050087 | TTGAGTAAGAGAGAG[A/G]GGAGATGACCCAGCT | 5521 |
rs368926758 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843900 | ATTGTGAATAGTGCC[A/G]CAATAAACATACGTG | 5521 |
rs368932241 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862026 | AGTGAAAGAACACAC[A/G]CATAAACACGAGTGA | 5521 |
rs368933009 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599876 | ACTATTTTAAGAGCA[A/T]GCATTTCCTGACTAG | 5521 |
rs368943787 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753663 | AGATAAGTGAGAAGT[A/G]GGAGGACCCAGAGGA | 5521 |
rs368945265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793149 | CTGATGCATTGCATG[C/T]GGAGTGTGAATAAAG | 5521 |
rs368950904 | in-del | -/AG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828000 | CCATGGCCTAGTTGA[-/AG]AGAGAGAGAGAGAGA | 5521 |
rs368958411 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014142 | ATGAAAAAATGCTCA[C/T]CATCACTGGCCATCA | 5521 |
rs368958541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818389 | AGGATTTTTATAATC[C/T]CTTCAACACAATCTC | 5521 |
rs368966075 | snp | A/G | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864174 | ATTGGAAAGAATCTA[A/G]ACTTCCATCATTAGG | 5521 |
rs368969355 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976567 | CAATTGGCACAACAC[A/G]ATTTACTGAAAAAGA | 5521 |
rs368970947 | in-del | -/T | 0.0130921 | 0.0798413 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030452 | AAGCTTGCTGAGAGA[-/T]TTTTTTTCATGCTTA | 5521 |
rs368975511 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935033 | AATTATGTATTGAAC[C/T]TATATTAGTTTCTAG | 5521 |
rs368976371 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881613 | AGATGGGGTTTTGCC[A/G]TGTTGGCCAGGCTGG | 5521 |
rs368994924 | in-del | -/CTC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903389 | TTTCTTGCTTTCTTT[-/CTC]TTTTTTTTTTTTTTT | 5521 |
rs369002134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147059059 | AAGTTTTCCAAATAC[C/G]CTTGTCCTAAATCAT | 5521 |
rs369007483 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815725 | CTATCCCCACTTTTC[-/CA]CACACACACACTTTA | 5521 |
rs369011346 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800946 | acacacacacacaca[-/CA]tatacacacatgtat | 5521 |
rs369016890 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806418 | ATAGCTTGTGTATAA[C/G]CTTTAAGGTATTGCT | 5521 |
rs369017374 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008255 | TGCTCCCAACTTATG[G/T]ACTTTTTGTCAGGCT | 5521 |
rs369020922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839977 | TGTATCTTTAGCATC[A/G]CCTCTGGGCAAATAG | 5521 |
rs369055047 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690828 | TTCAGTACAGAAGGT[A/G]CTCAAGACATTTTAG | 5521 |
rs369074395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715911 | CTGGGCTCAGTCTTC[A/C]CTTTTCCATCATTGT | 5521 |
rs369075553 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731014 | TCAGCCATGTACGAG[C/G]TGTGAGTTTGGAGAG | 5521 |
rs369079769 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905870 | TTCAAAATAGCAGGA[A/G]TCAGCTTTTGGGGAT | 5521 |
rs369093215 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944344 | GATTTTCAAGCTTTA[G/T]ATCAGAGAGAGAAAG | 5521 |
rs369096122 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971802 | AATTACATCTTTAAC[A/G]TACTTTTTTTATTTT | 5521 |
rs369099939 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992094 | CAAAAAGAACAAAGA[A/G]TTATTAAACCACCTG | 5521 |
rs369106586 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995647 | TACATGCCAGGATTG[C/T]CTTTTGATGACTTAG | 5521 |
rs369109545 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681130 | ATGTCCTCTATTGAG[C/T]TGGATTCCAAATCCA | 5521 |
rs369110472 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706046 | GGCATGGGCAAGGGG[C/G]GGGGGTCCCCAGGCA | 5521 |
rs369110823 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692653 | ATTCTCCTACCTCAG[C/T]CTCCTGAGTAGGTGG | 5521 |
rs369113521 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721177 | ACTGGAGCTGTTTTT[-/C]CTCTGCCTCTAATAT | 5521 |
rs369114995 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763214 | CCTGCTCAGGGTCTA[A/G]TAAGCAAACATGAAG | 5521 |
rs369115188 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765025 | TAGAAAACACATAGA[A/G]GTTTCAGAAGAATAA | 5521 |
rs369119422 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834658 | TTTTCTTTAAGTTTA[A/G]GTTCTGGGAGTACAC | 5521 |
rs369124852 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735333 | CACCAAAACCCCCCC[A/C]ACAATCCTTCTACTC | 5521 |
rs369130973 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957987 | ATAAAGTGAACCTAG[A/G]ACTGACAGAAAAGGG | 5521 |
rs369134388 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770126 | TTGAGGTCAGCAGTT[C/T]GAGACCAGCCTGGCC | 5521 |
rs369141819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626324 | TAAAGATTGTATGAT[A/G]AAATTCCCACCTTGT | 5521 |
rs369148595 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655341 | CCTGGGAAGCTCTTC[C/T]CCCCCAGAGAGTGGC | 5521 |
rs369161902 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623709 | CAGGTTAAAAAGAGA[A/T]GATAAAGGCAAGTAT | 5521 |
rs369162685 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078087 | GCAATGTACTTAATA[A/T]TTTTTGTTTGTTTGC | 5521 |
rs369163140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923267 | AACAAGTATGACAGA[A/G]GTCTGAAGGACCAGA | 5521 |
rs369163241 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706725 | TCAGTCTTTGTAAGA[C/T]GCAGGTCTTCCCAGC | 5521 |
rs369171641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814602 | ATGGGCTCAAGCATG[C/T]GCACTAAGGCAAAAT | 5521 |
rs369173353 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823230 | TGAGATGGAGTCTTG[C/T]TCTGTCGCCCAGGCT | 5521 |
rs369180442 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960358 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 5521 |
rs369192203 | snp | A/T | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857567 | GATAAAATCACCACC[A/T]GCCAGTACTGATACT | 5521 |
rs369201418 | in-del | -/ACTC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791603 | ACTCTCTTCACACTC[-/ACTC]CTCAAAGCTCTCCAA | 5521 |
rs369211957 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070996 | CCGTCTTGAAAAAAA[-/A]TAAAATGAAGTGGGC | 5521 |
rs369216516 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071596 | TGTACTGGCTGTTCC[C/T]TCTATCTGGAACTCT | 5521 |
rs369217423 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800331 | TCACAACTGTGTATT[A/G]TAAGGATCCCCGGGT | 5521 |
rs369224281 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991866 | ATTGATAAAATAAAC[-/T]GTAGAAGACATAAAT | 5521 |
rs369225304 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927761 | TTTTTTTAGATGGAG[A/T]CTCACTCTGTCACCC | 5521 |
rs369226679 | snp | A/G | 0.000214697 | 0.0103587 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691226 | CGCTGACTTTCCACA[A/G]CTTCACAGTTTTATC | 5521 |
rs369232596 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738395 | GTGAGACTCAGTCTC[-/A]AAAAAAAAAAAAAAA | 5521 |
rs369232750 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932885 | GATCAAGAAGACTTC[C/T]TTGAGCAAGGGGGCA | 5521 |
rs369235255 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912404 | GAAGAGTAGTGGGGA[A/G]AGAGTGAGCATTCTG | 5521 |
rs369241841 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916884 | TCTGCCTCTTAATAG[A/C/T]TGTGTAACTTTTGAT | 5521 |
rs369243043 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901442 | AGGTCAAGGCTTCAG[A/T]GAGCTGTGTGATCGT | 5521 |
rs369244924 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934577 | AGAAGAGGTAGTTTT[C/T]CATAAGAAAAAAAAA | 5521 |
rs369255534 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967149 | TGTTTTCACTGCAAC[A/G]TACTGCCCTCTATTA | 5521 |
rs369275837 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696592 | TTAAATAGCAAAATT[A/G]AAAGGAAAGAAATTG | 5521 |
rs369280093 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675998 | TATGACCCTCCAAAC[A/G]ATTCAATCACTCATG | 5521 |
rs369291399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861205 | GGACTACAGGTGCCC[A/G]CCACCACGCCCGGCT | 5521 |
rs369304070 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653167 | AGGGTTGCCCAGCTA[C/T]AGGAAGCATAGCTAG | 5521 |
rs369311558 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852942 | CTTTGGATTATCAGC[A/C]TTAAGAGGCAAGATT | 5521 |
rs369311865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948864 | CAACAGAAGTATGCA[C/T]ACATACCATGAGGGC | 5521 |
rs369323994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827402 | GGTAAAATACAATAC[A/G]AATAAAAGGGAAAGA | 5521 |
rs369325004 | in-del | -/TTTTTTCTTTT | 0.488424 | 0.0751925 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861048 | AGCATTCAAACTGAA[-/TTTTTTCTTTT]TTTTTTTTTTTTTTT | 5521 |
rs369336730 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671545 | CAGTAGTGCCTAATA[C/T]TTACTGTGGGCTTTC | 5521 |
rs369347745 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652774 | CACCCCCCCCCAAAA[A/G]GTTTTGCCATTATTC | 5521 |
rs369347899 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727597 | ATTTAGATAGGTGCA[A/G]TAACAGCCCGGACTT | 5521 |
rs369378009 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893745 | GTGGGGAGAGCATTA[A/G]GACAAATACCTAATG | 5521 |
rs369378462 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843778 | CTACAAAGGACATGA[A/T]CTCATCATTTTTTAT | 5521 |
rs369404808 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693697 | ATTTGTAAACTGGGG[-/A]AACAGTATCTTCCTC | 5521 |
rs369406224 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988090 | TGTAAATATATATGC[A/T]CCCAACACTAGAGTA | 5521 |
rs369434109 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644180 | CAATAAAAGAATATC[A/G]TAATGCAAAAAAAAG | 5521 |
rs369441916 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596198 | TGGTTTGGAACACAC[A/G]TTGCAGTCTGCCAAC | 5521 |
rs369442889 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615939 | ATAGCCAAGGCTATC[G/T]TAAGCAAAAAACAAA | 5521 |
rs369444491 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963918 | ATTGTAACAGCTTGA[A/C]CTTTCAGGTCTCATT | 5521 |
rs369457775 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751110 | CAAGCTGTAAGCACA[C/T]TAGGAAAGAGTAAGG | 5521 |
rs369467670 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966347 | GTCCACACTGATTTC[A/G]GCTTGTTGACTTGCA | 5521 |
rs369473877 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043326 | CATTAAGGAGGTAAT[A/T]ATGGTTAAATGAGGT | 5521 |
rs369475866 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634558 | CAGGCTGTTCTCAGA[C/T]TCCCAGCCTTGGGTG | 5521 |
rs369477149 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994045 | GCAGGTTGTGGCTTC[C/T]TAAGGTCAAGGCAGA | 5521 |
rs369488397 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599653 | TTTGAACACACTGTG[C/T]TTTTAATTATTACAC | 5521 |
rs369488619 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771620 | TACCAATATCAGTCC[G/T]GCCCTTCTTGAACAA | 5521 |
rs369488634 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606472 | AAGCAGCTTGACTCC[C/T]TCCAAGCTTCATTTA | 5521 |
rs369494437 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955930 | ATTACAGATGCCCAC[C/G]ACTGTGCCCGGCTAA | 5521 |
rs369494817 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983327 | CTGGGACTACAGGCG[C/T]CCGCCACCACGCCCG | 5521 |
rs369496152 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639337 | ATCTGGGTTTTTTTT[-/T]CTCAGTATTTCCCTT | 5521 |
rs369502645 | in-del | -/ACCTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655064 | TCAGTCCTTGGCCTG[-/ACCTG]TCTGCAGGTGGTTCT | 5521 |
rs369510399 | in-del | -/CA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890039 | ACATCCGCACACACA[-/CA]ATGGCTCTTCTTAAC | 5521 |
rs369522871 | in-del | -/ACAAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053261 | AGCAAACAAAACAAA[-/ACAAA]CAAACAAAAACAATG | 5521 |
rs369531890 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920761 | TGTGTCCTTTTATGC[-/TG]TGTGTGTGTGTGTTT | 5521 |
rs369532503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730579 | CAGGCAGAGGTAATT[A/G]CATCATGAGGGCCAG | 5521 |
rs369533426 | snp | C/T | 1.68704e-05 | 0.00290429 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589905 | AAAAACTTGTTTGAC[C/T]AGTATTCAGTATGTG | 5521 |
rs369536959 | in-del | -/CTCT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675834 | CTTCTCTCTCTCTCT[-/CTCT]GGCCCACTGCTTGCA | 5521 |
rs369537500 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819366 | TGAGCACATTCTCAA[A/G]AAATCATCTGGAGTA | 5521 |
rs369539990 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781930 | AAGTTGGAGGTGGGG[C/T]CTGGTGAGAGGTGAT | 5521 |
rs369541268 | in-del | -/GAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837466 | GTTGTATGGGGGTGG[-/GAG]AAGAAAGTGATGTGG | 5521 |
rs369546506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913078 | TTTGGAATGCAGCTG[C/T]CCTCTGGAGGCCCTG | 5521 |
rs369555016 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045360 | GGAAATACTTACCAT[-/T]GTGTTACAATTGCCC | 5521 |
rs369559334 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856761 | TCAACACTGTAAAAG[C/T]TTCCTTGCCTCAGCC | 5521 |
rs369561578 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831954 | ACATTGATAATCCTG[A/T]CCCTGTGTAGGCCTA | 5521 |
rs369563287 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952192 | CCCTTTCTTTCTTGC[C/T]CTGTTGATTTTTTAA | 5521 |
rs369563442 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873714 | CCTCCTGGGTTCATG[A/C]GATTTCCTGCCTCAG | 5521 |
rs369566019 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823118 | AGCCCCCTGTTCTGG[C/T]TTCAATCTGGAGATT | 5521 |
rs369583703 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892716 | GTGTTCTGGGAAAAG[A/T]GGTGCAGTTTGAAAA | 5521 |
rs369586286 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774750 | TGAGCCTGGGAGATA[A/G]AGGCTGCAGTGAGCT | 5521 |
rs369596595 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799486 | TTTGTAAGGAGGTAT[A/C]GACAGGCTACAGTCA | 5521 |
rs369601139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835224 | CTTAATAATAATTCA[A/G]TTTAATAATAAACAA | 5521 |
rs369613708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043441 | AGTTGAGAAGACGGT[C/T]GTCAGCAAGCCAAGG | 5521 |
rs369618912 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631437 | TCGCATGCTGCTTTA[A/G]CATTCATAAACATCT | 5521 |
rs369635712 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792558 | TGTTAGAAGGTGACT[A/G]TGGGAAAGCAGAATA | 5521 |
rs369635747 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680759 | AAACTCATCTGATCA[C/G]AACAACAAATTACAA | 5521 |
rs369659820 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975532 | ATATCTGAAGTGGAA[C/T]GGCTGGATCATATGG | 5521 |
rs369663372 | snp | G/T | 8.26426e-05 | 0.00642763 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701207 | AAAGGATAGATAATA[G/T]ATATACTTTTCTGTG | 5521 |
rs369679387 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793881 | CTGAGGTATCTAAAC[A/G]CAGGGAGACCAGTTT | 5521 |
rs369680489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606506 | GAGATAATAGTAGTA[C/T]CTATGTTCTAGGGCG | 5521 |
rs369705250 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637283 | TCAACTGGGAGCAAT[A/G]TTTTCACCAAGAGGG | 5521 |
rs369707932 | in-del | -/C | 0.143959 | 0.226396 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632062 | ATGGGCTGAGTTGTG[-/C]CCCCCCCCCCGCCCA | 5521 |
rs369715096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709949 | CAGGTTATTAATGCA[C/T]GTTGAGTTGGAAACT | 5521 |
rs369716922 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686714 | GATTTCAACCTGGCC[A/T]AGGTTCCCAGGGCAC | 5521 |
rs369726061 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752536 | AGAGAATAAGTGCCA[C/T]GTCTGCTTAGTTTAT | 5521 |
rs369727913 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805478 | TTGAAAATGGAAAGC[A/G]GATAGATCATTCCTC | 5521 |
rs369735278 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022482 | GGGGAATCGCTTGAA[C/T]GTAGGAAGTGGAGGT | 5521 |
rs369739229 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821125 | TCACATACTAAAAAA[-/A]TATCCACAGAGAAAC | 5521 |
rs369740120 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991925 | TTGGAAATATTAATA[G/T]TATTAAAATATTTAT | 5521 |
rs369743673 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705341 | AAAATATATTTCATA[A/G]TGAATGATAATGGTG | 5521 |
rs369754580 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924850 | CAGCTTCATCCATGT[A/C]CCTGCAAAGGACATC | 5521 |
rs369759664 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986505 | TGAAGATGCTCAACA[A/C]ATTTCAGTAAAACAC | 5521 |
rs369760758 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657971 | GAAGGTTATAACCAC[A/T]CACTGGCCCCAGATA | 5521 |
rs369766401 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635378 | TTTCATCATCCAGGT[A/G]TTAAGCCTAGTACCA | 5521 |
rs369772882 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865582 | CTACATTTAATTTTT[A/C]AATATTTTATACCTA | 5521 |
rs369778654 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708969 | CACTCATTTAGTTTG[G/T]TACTAAAGACAGAAG | 5521 |
rs369783893 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750836 | AAAATAAAACAGTTC[A/G]AATACACACGTTGGT | 5521 |
rs369784745 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665013 | TAAACAGATGTGCTC[-/C]TATTCAGGCTTTGCT | 5521 |
rs369790526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730410 | AAATGAGTTAAGACT[C/T]TGGGGGACTACTGGG | 5521 |
rs369799711 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741222 | AGGAAGGTTCTTGTC[C/T]AGCAGGCAACCCCCC | 5521 |
rs369804406 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810505 | AGATGAGATTTGGGT[A/G]GGGACACAGCCAAAC | 5521 |
rs369806438 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779702 | TGGTCATAGTCTCAT[C/T]CCCGGGTTTAATTTA | 5521 |
rs369808593 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721802 | TGAGCCACGCATACC[A/T]CTTAAGTAGCTCTTG | 5521 |
rs369822381 | in-del | -/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699661 | TGCGAACTTAATTGG[-/TT]TTTTTTTTTTTTTTT | 5521 |
rs369826714 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885801 | AGCTGCAGAAAGGAA[C/T]GAAGTATTGAAACAT | 5521 |
rs369829404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593787 | TGAGTAAGCAGCTGG[A/G]GGAGAGGATGATCAG | 5521 |
rs369833055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862473 | ACATTCGTGAAATGG[A/G]GAAAATATCTATAAG | 5521 |
rs369839833 | in-del | -/AG | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758669 | GTACCAGTACCTAGT[-/AG]GAGCTTAATACCTAC | 5521 |
rs369841298 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874010 | CTTCTACCTAAAATG[C/T]TTTCAGGTCTTGTTA | 5521 |
rs369857137 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999380 | AATCCTCCCACATTT[A/G]CCAGCCCCATCATTC | 5521 |
rs369860032 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067398 | TTCCACAGATGTGAG[A/G]TCATCTGGTATTTGC | 5521 |
rs369877585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940543 | AAGGCTACTGCCCAA[A/G]GAGAACATATCTAAA | 5521 |
rs369888043 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910504 | TGCCATATGATTGTT[G/T]CTTCCTTTACTCTAG | 5521 |
rs369895591 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628587 | CTAGACATTACCTCT[C/T]AATAAGATGGAAGCT | 5521 |
rs369900869 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979638 | GATACGTTCCAAGAC[A/C]CCCAGTAAATGCCTG | 5521 |
rs369905068 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016118 | AGGCAGGTACATTGC[C/T]TGGTCCCAGGAGTTC | 5521 |
rs369909904 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953330 | ATGTCTGAAATGTAA[C/T]ACTCCAGTTCATTTG | 5521 |
rs369915420 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692565 | TTGAGACAGAGTCTC[G/T]CATTTTCACCCAGGC | 5521 |
rs369924155 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918057 | CTGGCACTGGCTTTC[C/T]TTGAAAACATATAAT | 5521 |
rs369931023 | snp | C/T | 0.0001154 | 0.00759518 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600341 | GATCCCAGACTTTGA[C/T]GGTCAAGTAGTCCCT | 5521 |
rs369939158 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881932 | TGAAATAATTGGTTC[A/G]ATTTATTCCTGTATG | 5521 |
rs369950676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869441 | CATACTATGGAGCAC[C/T]GTGCAGCCATTAAAA | 5521 |
rs369971270 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911336 | ATCCTCCCACCTCAG[C/T]CTCCCAAAGTGCTAG | 5521 |
rs369975988 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649579 | CCTCCCAAGTAACTG[G/T]GACTACAGGCGCCCG | 5521 |
rs369978119 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660471 | AACCTCACTTTGGTC[A/G]AAAAACCTGTTTCTT | 5521 |
rs369978785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060751 | TGCTGTGAGGATCAA[A/G]TGAGGTAATCCAATA | 5521 |
rs369982306 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014215 | CAGTTAGAATGGCAA[G/T]CATTAGAAAGTCAGG | 5521 |
rs369984355 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616718 | CTTTCATCTAAAAGG[C/T]AATAATGCTGATGAG | 5521 |
rs369993049 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636994 | CTGTGAGGTCTGTTT[C/T]AAATGTCTCAACCGT | 5521 |
rs370025208 | in-del | -/A | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862877 | AAAAAAAAAAAAAAA[-/A]CCCTGGCTTACATAA | 5521 |
rs370034952 | snp | C/T | 0.000199379 | 0.00998246 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:146856545 | ATTCATGCTTCATTA[C/T]TGGGCCACTATTCTC | 5521 |
rs370065252 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788750 | CAACACAACAACAAA[A/T]ATTATGGTGAAGGGT | 5521 |
rs370072633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846784 | TCTTGGAATGATGCT[A/G]GTCTAGAATATTCCT | 5521 |
rs370072849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054687 | AACAAGAGTGGGTTT[C/T]CAGAACAGGCTGGTC | 5521 |
rs370087136 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639260 | GGAGTTTTTAAGTAT[A/C]AGAAACAAGCCATCC | 5521 |
rs370087995 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706526 | ACGCAGCTGCCGCGC[C/G]ATGTCCTACTTGGTC | 5521 |
rs370112528 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748351 | TTCACCCAGTTCCCC[C/G]CATCACAATGGTAAC | 5521 |
rs370139059 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035808 | TGAAGGGAAAAAAAA[A/C]CAGTTTGGATGTCTA | 5521 |
rs370141696 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880882 | TTGGATAGGTCTCCA[C/T]TGTTTAAGTAGATTT | 5521 |
rs370149910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655528 | TGAATTTTCATCGCT[A/G]TCCTATGATTAACTT | 5521 |
rs370157732 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937298 | AGAGTGAGACTCCGT[C/T]TCAGAAAAAAAAAAA | 5521 |
rs370166891 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747204 | CTGAGTCAGAAAAAA[-/A]TGGCTCTTGTCTCCC | 5521 |
rs370169214 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830317 | CACAGTATCTGACAC[A/C]AGCTAATGCCTATAA | 5521 |
rs370172663 | snp | C/T | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860840 | AGTCCCCTTATAAAA[C/T]GATTGGCTGAGATCA | 5521 |
rs370176510 | in-del | -/ACAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077276 | TATGTATGTGTGTAT[-/ACAC]ACACACACACACACA | 5521 |
rs370182963 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694934 | CAAATATATTTATAG[A/G]GATAGAATATATTTG | 5521 |
rs370186954 | in-del | -/CCCTCCCACCACCTCTCTCTGC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892506 | ACCACCTCTCTCTGC[-/CCCTCCCACCACCTCTCTCTGC]TTAGCATATATGATT | 5521 |
rs370193194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689408 | TATGCTTAGATATGT[A/T]TATATACACAAATAC | 5521 |
rs370195005 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590168 | CAAGGGTCACATCAC[A/G]CTTGGTGTTTCTGTC | 5521 |
rs370199631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076118 | ATGCTCTTAATCACT[A/G]TATCACACTGCGTTT | 5521 |
rs370201626 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714112 | ATCCAGGGAAAAAAA[A/C]AAAGAGAATGACCAG | 5521 |
rs370203977 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021265 | TGATGAACCCTGGGG[G/T]AAGAAAGGGGCACCC | 5521 |
rs370219586 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976262 | CCTGCGTCAGCCTCC[C/T]GGGTAGCTGGGACTA | 5521 |
rs370227677 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771732 | CAAACAATTTTTCTA[C/T]TTTTCTTCGGTATAT | 5521 |
rs370242403 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870449 | GGCCATATGAGGACC[C/T]AGCAAGAAGTTGGCT | 5521 |
rs370248063 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022994 | GGAATAAAGGAATGA[-/C]AAAAATTAGAAATGA | 5521 |
rs370269821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913075 | TTTTTTGGAATGCAG[C/G]TGTCCTCTGGAGGCC | 5521 |
rs370270077 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628876 | ATAATTGATCCTAAT[G/T]TATTTCTAAATCACT | 5521 |
rs370285199 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684012 | TGAGAAATTACCCAT[A/G]CTAGAATGACACATT | 5521 |
rs370291939 | in-del | -/TTAT/TTATTTAT | 0.294832 | 0.245947 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670476 | GTTTTATGTGTACTA[-/TTAT/TTATTTAT]TTATTTATTTATTTA | 5521 |
rs370311425 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079505 | CTCAGCCATAAAAAA[G/T]AATAAAATCCTGTCA | 5521 |
rs370311835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031586 | TATCTCCTCAAATAT[C/T]GATATTGCTCATTAC | 5521 |
rs370325573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013013 | CCAAAATCTCCTTAA[A/G]CTGATAAGCAACTTC | 5521 |
rs370332162 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760268 | AGGTATTGCTTTAAT[C/T]TCTATTTTGCAGATG | 5521 |
rs370332986 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958868 | CAACAAACTTATGCA[A/G]TAGGTTCTATTATTT | 5521 |
rs370333390 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993520 | GTGCTGGGATTACAG[G/T]TGTGAGCCACTGCAC | 5521 |
rs370335974 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816026 | AAAGTTCTTTCAGCC[A/G]TTCCTAATATCAAGA | 5521 |
rs370337694 | in-del | -/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590396 | TTTTGTTTTTTTTTT[-/G]TGTTTTTTTTTTTTT | 5521 |
rs370350286 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832468 | GCGATGTTGGCTCAC[C/T]GCAACCTCCGCCTCC | 5521 |
rs370352271 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848586 | GATAAAGTGCCATTT[C/T]CATCCTATCACATCA | 5521 |
rs370365334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838482 | AGGCTGAGGCAGGAG[A/G]ATCACTTGAACCTGG | 5521 |
rs370373217 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882371 | TCATCTAATTTTAAT[A/G]ACGTGAACTTTCTTA | 5521 |
rs370374221 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676640 | CCATTCACCTTTCCT[C/T]TAGAGGCCCCATTAC | 5521 |
rs370374769 | snp | A/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801175 | CCAGGGCCTGAGGGG[A/G/T]TGGGGAAGGAGAACA | 5521 |
rs370378705 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899175 | AAGACACATGCACAC[A/G]TATGTTTATTGCAGC | 5521 |
rs370379469 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718491 | ACACACGTACATTTG[A/G]TTTTCAGTTGAATTG | 5521 |
rs370383934 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767591 | TAGACTTTTTTAGAG[A/C]AGTTTTAAGTTCACA | 5521 |
rs370391398 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633845 | CCCTGGGCTCTCCCC[A/G]TCTGCTTCTCCATCC | 5521 |
rs370408525 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941310 | AATACCAAAACACTT[-/G]GGGACCTAATTTTCC | 5521 |
rs370408747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961946 | TCCCTAGAGAACAGA[A/G]TGAATTAAGGAGTCA | 5521 |
rs370414288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700302 | TGGAAGCTCGAAGAC[C/T]ATGCCAGGGGAGGCC | 5521 |
rs370434594 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606910 | GATGAAAAAGGAACG[C/G]GCTCGGAATCATGCG | 5521 |
rs370441792 | in-del | -/TTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907913 | CTGGCTGATCAAATG[-/TTG]GCAGCATTGAATTCC | 5521 |
rs370454360 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914201 | ATTGACAGTTTGAAT[A/G]TTACAATACTTTTAA | 5521 |
rs370459310 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672605 | CCAACACAGAAAACT[A/G]CTTGCAGAAACTGAG | 5521 |
rs370487845 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038779 | TAAGTTGCTCAACGT[C/T]ACTTAGCTAGTAGGT | 5521 |
rs370505604 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965191 | GAAAATCATCCACCA[A/G]CTCCCTTCAAAATAT | 5521 |
rs370509105 | snp | A/C | | | stop-gained, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650617 | GGACATGTAGGTTTC[A/C]TAGTCGCTGTTGACA | 5521 |
rs370529578 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595176 | GGTGACAAGGGAATA[C/T]CCCTACAGCAGTGCT | 5521 |
rs370539151 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633796 | GGTGTGTGGCTTGAC[C/T]GGCTTCCTGCTTCTG | 5521 |
rs370543753 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620324 | TCTTTCTTTTGTGAG[A/G]AATAATCATTTATTA | 5521 |
rs370568747 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647957 | TTCTCATTGTCTCCA[A/G]ATATATCTCATAATT | 5521 |
rs370578905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867118 | TTTCATATGAAAAGT[C/T]AGTTGAAGAATTTCA | 5521 |
rs370580338 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888174 | ACAGTCCCACAGCTC[A/G]CCACTCACATAACAA | 5521 |
rs370580369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885957 | GTAGATTAGTGGTTG[C/T]CAGGGACTGAGGATA | 5521 |
rs370582466 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996550 | CCCTAAATAGGAGTA[C/T]GGTTTGCCCATAGAG | 5521 |
rs370587677 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014299 | GGTGGGACTGTAAAC[A/T]AGTTCAACCATTGTG | 5521 |
rs370596265 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929350 | AATGTGCCTGGCATG[A/T]AATAGACATTCAAAA | 5521 |
rs370603458 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645310 | GTTGCTTGATGATGA[A/G]ACACTGGAAATCTCC | 5521 |
rs370604729 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686828 | CAACTTCCATTTCAG[A/G]CTGATTAAGTCACTT | 5521 |
rs370606225 | in-del | -/ATTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931751 | TATCTATGTGTTCTA[-/ATTA]GCCCCACCTTAGCTT | 5521 |
rs370607511 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018310 | CTATCATCCAGTCAT[-/G]ACATAGCCACCATGA | 5521 |
rs370607621 | in-del | -/TCAT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912834 | GATTCATTCATTCAT[-/TCAT]CTGCTTATTAATTCA | 5521 |
rs370610472 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819852 | TCACAATAGCCAAGA[A/T]AAGAATTGAATGTAT | 5521 |
rs370611328 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875721 | CAAGATCTATGGAAG[A/G]ACTAGAAGCTAATTC | 5521 |
rs370615054 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885972 | GAGGATAAAAAAAAA[-/A]GGGGTGGGAATGACT | 5521 |
rs370615604 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849633 | GGGCAAACAGTACAA[A/G]AGGGTGCACTAACAA | 5521 |
rs370616218 | in-del | -/TGCCCTGT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677042 | TAACTCCTGAACTCC[-/TGCCCTGT]TATCTTTGTTGTCTG | 5521 |
rs370618623 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892461 | AAAATATACATGCAC[A/T]CATGCACGTGAGCAC | 5521 |
rs370641103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942399 | TTTCTTATACCGTCA[A/G]AAATAAGTCAAGTTC | 5521 |
rs370643846 | in-del | -/CTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670455 | ACCCCTTCAGATTTT[-/CTT]ATCTGTTTTATGTGT | 5521 |
rs370670139 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719741 | TTTATTTTATTTGGA[A/C]TAGTTTATTAACATT | 5521 |
rs370682349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883682 | CTCTAAGGTGGTTTA[C/T]GTGCTGTCTAGAGAA | 5521 |
rs370695245 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954709 | CTTTAGAGAAACACA[A/C/T]GCACCAGTACATATG | 5521 |
rs370713407 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630281 | AATTCAAAGGCTTTG[C/T]CACATACCACTACTT | 5521 |
rs370713730 | snp | A/G | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918505 | ATTCACAACTTCTCT[A/G]TATAGCCCTCTCATT | 5521 |
rs370718914 | snp | C/T | 0.000169986 | 0.00921759 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856478 | ATCAAGAAGAGTAGG[C/T]ATAAATAATAATACG | 5521 |
rs370723346 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743785 | ACTGTTACACCAAGT[C/T]GTAAGCTAAAATGTG | 5521 |
rs370724509 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615151 | ATGTGGCACATATAC[A/G]CCATGGAATACTATG | 5521 |
rs370726521 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888429 | TCACCATCTCCACTG[A/C]TGCTACCATGCTCCA | 5521 |
rs370728130 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012596 | CAGTTCTGCTCTGAT[C/T]TTAGTTATTTCTTGC | 5521 |
rs370734951 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789998 | TTGACTGAAATGCAG[A/T]GGTAAAATGTAATCA | 5521 |
rs370743138 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945110 | GCACTTTAATGACCC[A/G]TGTTAAATCTCTGTA | 5521 |
rs370754913 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811623 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 5521 |
rs370757971 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936776 | ATTTACTCCTTGCCA[G/T]GTAACTGGGGATCAT | 5521 |
rs370769822 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660581 | GTTTCCAGAATGAAA[-/C]CTGCCACTCACCAGC | 5521 |
rs370772278 | in-del | -/TGTG | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880180 | TTGACATAGTTATTT[-/TGTG]TGTGTGTGTGTGTGT | 5521 |
rs370787312 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785515 | ATTGTACCACTGCAC[C/T]CCAGCCTGGGCAACA | 5521 |
rs370790548 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802721 | CAGTTTTTCCTCAGC[C/T]TGGACACTCCATATC | 5521 |
rs370798865 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048107 | TGATTCTCACGCATA[C/G]CCAGGGTTAAAACCT | 5521 |
rs370800412 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824046 | AACAGGTTTCCACTG[G/T]CATCTTCTTCACTTA | 5521 |
rs370803080 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772225 | ATTTATCCCCTAAAA[C/T]AGCAAACATTTATAG | 5521 |
rs370803300 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854634 | CTAAACTTGTGAAAA[C/T]GACACCTTGAAGTGA | 5521 |
rs370806992 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724922 | GGAAAGGGAGAACAC[C/T]GCTCAATAGGGTTTT | 5521 |
rs370812764 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765121 | CCAAATCAGTGAAGA[C/T]TTCTTATATGCTATA | 5521 |
rs370815916 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870817 | ACATTTGTTGTAAGC[A/G]ATCAAGTCATTTACC | 5521 |
rs370819940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885617 | AAATTTCACTTCTAT[A/G]TATATATTGAAGAGA | 5521 |
rs370823280 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811287 | ACAGGCGTGAGCCAC[A/G]GCGTCCAGCCATATG | 5521 |
rs370847953 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760647 | TCAGAAGTTAAGGTG[C/G]ACCTGGAATTATTAG | 5521 |
rs370852988 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791899 | GGTGCTGATTCCTCC[C/T]GCCACATGAGAGTGA | 5521 |
rs370866714 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843195 | TCTGCCTCAAAAAAA[-/C]TTTAAAATTATCCAG | 5521 |
rs370870740 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845392 | CTCACTGCAAGCTCC[A/G]CCTCCCAGGTTCATG | 5521 |
rs370870929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009435 | ATAATTCATATTTCT[C/T]TGAAAGCAGATAATC | 5521 |
rs370875443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828076 | TTCTTTCATGGTGGC[A/G]TCCTGGCTGCTGCAA | 5521 |
rs370881889 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726652 | GTTAGTAGTGGAGCT[A/G]AGATTCAAACCCACA | 5521 |
rs370891716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046832 | GCCTGGTGCTCAGTT[A/G]GTTTTTATTAAACTT | 5521 |
rs370897003 | in-del | -/T | 0.00893928 | 0.066255 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777621 | ATGGTAAATTTTATG[-/T]TATATATATTTTACC | 5521 |
rs370904981 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008271 | ACTTTTTGTCAGGCT[C/T]TAGTTTCTTTAGAAA | 5521 |
rs370909071 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968274 | GTTTAGGGACATTCT[C/G]GGCTTCCTTGTATTC | 5521 |
rs370925731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907203 | AGCATGAATTGGCTA[A/C]ATTACATTTTTTTTT | 5521 |
rs370935979 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648500 | ACCTACTATTATTTC[A/G]AACTTGACAGGTTCA | 5521 |
rs370939048 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680121 | TGTGGCATTATTCAC[A/G]ATAGCAAAGACTTGG | 5521 |
rs370939071 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722699 | AACAATAATGAAAAA[A/G/T]CCTGCAATGCTGAAC | 5521 |
rs370950736 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685006 | TTGTAACTTGTCTCC[A/T]CCATGCCCCCTAAGG | 5521 |
rs370953967 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758478 | ACAAATACGGCACTA[A/T]CATGATGAAATAACA | 5521 |
rs370964606 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816249 | TCTCTACAAAAAAAT[C/T]AAAAAATTGGCTGGG | 5521 |
rs371003761 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928841 | TTTCAGTGACTTACA[A/G]TACTCTTCATAGTCT | 5521 |
rs371011329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066049 | CAACAGACTGACTCC[C/T]GAGTCAGGTTGTTAA | 5521 |
rs371027373 | snp | C/T | 4.94466e-05 | 0.00497201 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638326 | TGCTGCTGCTGTACA[C/T]GAAGGTGTTGCAATG | 5521 |
rs371033768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060106 | TACTTTTAAGTCAAA[C/G]CAAAGCAAATTCCTA | 5521 |
rs371035075 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045608 | AATGTATTCTCCTCA[C/T]AGCAGTCCCAAAAAT | 5521 |
rs371040931 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961542 | TATTTTGTTCCTTTA[A/G]TTACTAGGAAGCTTG | 5521 |
rs371060050 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018467 | ATCTCATTTTTTATA[A/C/T]ATATTTTTTAAAAAC | 5521 |
rs371061517 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633533 | AGATGTGCACTGAAG[A/G]AGGTTGGTTCTTTGA | 5521 |
rs371076765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595352 | TTAAGGTCTAGTTCC[A/G]TATGTCTGCTTTGTG | 5521 |
rs371082117 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897956 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 5521 |
rs371084550 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031153 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 5521 |
rs371088468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993134 | TTTTAGTAGAGACAG[G/T]GTTTCACCATGTTGG | 5521 |
rs371093137 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914924 | TTTCAGTATTCGAAT[C/T]GACAGTGGCTTCCAA | 5521 |
rs371100461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806844 | ATGCAAGACACTGCC[A/G]CCACCTGAGGAAGTA | 5521 |
rs371100687 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147080636 | GGATTCAATGTTCTC[A/G]TAAGTCATATGACTA | 5521 |
rs371108173 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823476 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 5521 |
rs371110855 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670564 | GCAGTGGCGCAATGT[C/T]GGCTCACTGCAACCT | 5521 |
rs371110873 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681684 | TGAGAAAATCCTATC[C/T]GGGTCAGTGTGAATC | 5521 |
rs371113500 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056900 | TTGTATATAATGAAG[A/G]GAAAGAGTCAAATGT | 5521 |
rs371117333 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073083 | GGAGCAACAGGGTTT[C/T]GTCCATGACTGGCCT | 5521 |
rs371118947 | snp | A/G | 0.000122774 | 0.00783401 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697945 | AGTTTGGCCGACTGT[A/G]TCTCTGAAAATACCA | 5521 |
rs371121436 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630045 | TCTCGAACCTCCTGG[C/T]CTCAAGCAACCCACC | 5521 |
rs371134234 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981027 | AAAGGACTCAGTGAA[A/C]CTTCAGAACATTTAA | 5521 |
rs371136255 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026395 | TGAGTTTATATATAT[A/G]AAATTCTAGAAAATG | 5521 |
rs371136387 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997855 | TAATTAAGGCAAATA[C/T]AAGTGCTGGGTTTTG | 5521 |
rs371147548 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772405 | ATATATATATATATA[C/T]ATATATATATATATA | 5521 |
rs371147648 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007445 | AAATGCACCAATCAG[C/T]ACTCTGTAAAATAGA | 5521 |
rs371151852 | in-del | -/GGA | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837465 | AGTTGTATGGGGGTG[-/GGA]GAAGAAAGTGATGTG | 5521 |
rs371156441 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639217 | CTTCTAGTCTCTGTA[A/T]GTTGTGATCTGCTTT | 5521 |
rs371167467 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759765 | TCTTCCCTTTTTTTT[C/T]TTTTCATTTGTGACG | 5521 |
rs371181664 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796418 | ATAGAACACCACTTC[C/T]GTGGCATCTGACTGC | 5521 |
rs371189681 | in-del | -/GTT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912999 | CTTGCAGAAAATGTT[-/GTT]AAAAACACTATGTGT | 5521 |
rs371196271 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065784 | TCTTGGGTGTTTGGG[A/G]GGGCTTTCGGAGGAA | 5521 |
rs371199295 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707887 | TTTTTGGTGTAGAAC[A/G]TACATAATTTATTTT | 5521 |
rs371201406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845227 | CATCTAAAGCCATCT[C/T]ATCATTATCCAGTAT | 5521 |
rs371201466 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832902 | ACTCTGGTGTTCACA[C/T]AAGGATGAAATTGCC | 5521 |
rs371201754 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830979 | TGCAGCCATCATAAT[A/G]CCAGAGTGCAATGCA | 5521 |
rs371203172 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033988 | CAAAGGTTTCCTATT[A/G]CACTGAAAATAAAGC | 5521 |
rs371204215 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846867 | CTTAAACCTGCCTAT[A/G]ATGGTATATATTGAG | 5521 |
rs371209088 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866463 | ATTTTCTCTTTCACT[C/G]CATAAGTGTGTAATG | 5521 |
rs371217502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980815 | AGATACAAGATTTCA[C/T]ATACATACATGTTTG | 5521 |
rs371260472 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944326 | GGGAAGAGATTGAAA[A/G]GAGATTTTCAAGCTT | 5521 |
rs371263287 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915614 | TAAGTTTAGCTGTCA[C/T]ACTCAGGTGCAGAGT | 5521 |
rs371270857 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990064 | TAAAACCATAAAACA[G/T]TAATGAAAGAAGCTG | 5521 |
rs371271781 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794003 | CTCAGAAATTTCATT[C/T]TGACACATATCTCAG | 5521 |
rs371317115 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597384 | TCTTTTTAGTTCACT[C/G]CTTCTAGTATGTTGA | 5521 |
rs371322867 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651929 | ACTTTAACTCACCTA[C/T]GCGGGAGTTTTTAAA | 5521 |
rs371331798 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626733 | CTTTCCCATTCTGCA[G/T]GTCTTGGGGGCTGCA | 5521 |
rs371346109 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914908 | CCTACTAGTCCTCCA[C/T]TTTCAGTATTCGAAT | 5521 |
rs371353389 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651752 | TTGCAACTGAGCCCC[A/G]ACTGATTTGATACCA | 5521 |
rs371360427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616867 | AGCAATCCCACTCCT[C/T]ATGTATATACCCCAA | 5521 |
rs371368268 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062208 | ATGACATTCAGGACT[A/G]TACAGCCTTGTAGCC | 5521 |
rs371372787 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005983 | CAAGGGCATAACCCG[-/A]AAACACTGAGGCCAC | 5521 |
rs371375306 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014564 | TGCAGCCATAAAAAA[G/T]GATGAGTTCATGTCC | 5521 |
rs371380146 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009054 | AAATCCATTGCTGCA[G/T]TACTTTTAGAAAGCT | 5521 |
rs371399081 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988954 | AAATACAAAGGATCA[C/T]AAGAAACTACTATGA | 5521 |
rs371404265 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950635 | AATAAATATACAGCC[A/G]AAGAGTCACTGTTTA | 5521 |
rs371406958 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626999 | ATTCTATTTTTATTC[A/G]ATGGCTTGGGCACTG | 5521 |
rs371408368 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854884 | AAGCTCTTAAAATTT[C/G]GACTCTGAACTGTCT | 5521 |
rs371408485 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001952 | TCAGGGTCCTGACAA[C/T]AAGTTGGTTGACCCT | 5521 |
rs371413801 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666724 | GGTGAGCTCAGGCCA[C/T]TTGGCCTCCACAAAT | 5521 |
rs371419003 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913589 | TTAAAACAGCTCACT[C/T]GGTCTCTTGATCTCC | 5521 |
rs371436084 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057450 | TGGCCAGCAGTGAGG[A/G]AGTAGAAGGAGTGTG | 5521 |
rs371439718 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063521 | TCCAATTATTCAGTG[C/T]ATATAATGCCTCAAA | 5521 |
rs371439988 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685853 | TGTGTACCCACCCTG[C/T]GGCAGAAAAGGCTCT | 5521 |
rs371445624 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015477 | TGCCAATCTGAAGGT[C/G]CAAGTTTTACTCATA | 5521 |
rs371453352 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781267 | AGTAGTGTGAGTATA[A/T]CAACCCAGGTCTAAG | 5521 |
rs371454667 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030752 | AGAGAGCTTAATAAC[-/T]TTAACTCCCTTAATC | 5521 |
rs371466780 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966534 | GCCCCTCCCTCAACA[C/G]TCTAATCCATCATAC | 5521 |
rs371466868 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981981 | GGTCAATGATGGAGT[G/T]TCCTTATTTTTTGTT | 5521 |
rs371474427 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748317 | ATTGTAAGAAATAAT[A/G]GAGAGTTACTATGGA | 5521 |
rs371526147 | snp | A/G | 1.76194e-05 | 0.00296806 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697931 | AGATTGAAGTATATA[A/G]TTTGGCCGACTGTAT | 5521 |
rs371526307 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615298 | ATAGGTGGGAATTGA[A/G]CAATGAGATCACATG | 5521 |
rs371536098 | snp | C/G | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082932 | CAGGGCTAAAACTTC[C/G]TAATAAAATTAGCAC | 5521 |
rs371540157 | snp | A/G | 0.000313219 | 0.0125104 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593081 | GAGAGGAAACATATC[A/G]AGAAGGTCAGTTATT | 5521 |
rs371550575 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971812 | TTAACATACTTTTTT[-/T]ATTTTGGAATAATTC | 5521 |
rs371560791 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637497 | ATAGTGGCTTCCTAA[C/T]CTGTCTCCTTGTTTC | 5521 |
rs371571081 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884994 | ATTTCTAAAGAACAT[G/T]GCTTATAATCATGAA | 5521 |
rs371575129 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607093 | TTCAGAGACATGCAG[A/G]CAACAGTTTTGCCCC | 5521 |
rs371583202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964538 | TTTTATTTTTATTTT[C/T]ATTTTTATACGGAGT | 5521 |
rs371592472 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728297 | TATTATCCATTCCAC[C/T]GTGTGACTCCTATAA | 5521 |
rs371594264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678071 | CCCCCATGGCTCAGA[A/G]GGTTAAAAGCCATTG | 5521 |
rs371598592 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872725 | GGACTCTTCTTATCC[C/T]ACCACATTGCTGAGA | 5521 |
rs371617314 | snp | C/T | 1.70837e-05 | 0.00292259 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650747 | GCAAGAGAAACAAAT[C/T]ACTTCAGAACCAAAG | 5521 |
rs371617923 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044772 | GCCTTGCTGTTTCTA[C/T]AGGAATATATGCAGC | 5521 |
rs371619127 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708154 | TGAGCTCAGGAGTTC[A/G]AGACCAGGCTGGGCA | 5521 |
rs371625026 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882845 | ACTGACCTATTTCAG[G/T]CTTGTGCTTTACATA | 5521 |
rs371629924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895540 | TTTTTAATCTCATCA[A/G]CAGTTTTTTGTTTGT | 5521 |
rs371634985 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708682 | GTCTCTATTGATATG[A/T]CTCAACTTGATTTGG | 5521 |
rs371637328 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750230 | AAAATCAAGGAGACT[C/G]ATTCTTCCCAGTTTA | 5521 |
rs371639158 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027444 | TCGAGACCATCCTGG[C/T]CAACATGGTGACACC | 5521 |
rs371663270 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680247 | CATGTCCTTTGTAGG[G/T]ACATGGATGAAATTG | 5521 |
rs371671208 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937216 | TGAAGCAGGAGAATC[A/G]ATTGAACCAGGGAGG | 5521 |
rs371680750 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022787 | TAAACAGAGCAAACC[A/C]TAAGATAATGGGAGA | 5521 |
rs371684968 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713233 | ATGAAACTGACAATG[A/G]AAAGACCCTAAGAGG | 5521 |
rs371687847 | in-del | -/TACCAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728950 | TGGTACCAGGAGTGG[-/TACCAG]GGTGTTGCTGAAGAG | 5521 |
rs371688949 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631406 | ACCTTGCTGCATTCA[C/T]GGTGAGATTATCATT | 5521 |
rs371689225 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733149 | TAAATCAGTGGGAGG[G/T]GCTGTTCCCGCAATC | 5521 |
rs371703836 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897715 | AAATAAATAAATAAA[C/T]CCTAATTTGTATGTG | 5521 |
rs371726779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739633 | GCATGATAGGAAGAG[G/T]ATGCATCAAAGATTT | 5521 |
rs371730816 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707489 | CTGCCCACTCAGGAG[A/C]AGCTCAAGGAGCTGA | 5521 |
rs371730942 | in-del | -/ACCTGTCATTGCTATCCCTGT | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597330 | CATTGCTATCCCTGT[-/ACCTGTCATTGCTATCCCTGT]TGCTGTTGTTACCTC | 5521 |
rs371734856 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792575 | GGGAAAGCAGAATAG[A/G]TTAATGCAGATCAGA | 5521 |
rs371739360 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749723 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 5521 |
rs371742718 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813763 | CGAATAATCAAAAGA[C/T]GAGGAGACTTGCTTA | 5521 |
rs371745070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812122 | AACTAGTTCTGTGAC[A/G]TGTGGAAGTTTCCAT | 5521 |
rs371749693 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903719 | ACCACTGTTCTAATG[C/T]TTAAGAGTACATGCT | 5521 |
rs371753392 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830559 | AGATGGAGTCTCACT[C/G]TGTCGCCCAGGCTGG | 5521 |
rs371764568 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859897 | GTAGTATGAAGGACA[C/G]TTTTGTGTAGGGAAA | 5521 |
rs371779801 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146701127 | TGGTTGAATTCTACC[A/G]TAGAGATAATGTCAG | 5521 |
rs371782695 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797593 | GTATATTTGTAACCT[A/C]GTGCTTAAAGAGACC | 5521 |
rs371784848 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944185 | CTCCTAAGTGCAATA[C/T]GCTGAGACGTCTAAA | 5521 |
rs371794028 | snp | C/G | 0.0566069 | 0.158427 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022552 | TGACAGAGCAAGGCT[C/G]CATCCAAAAAAAAAA | 5521 |
rs371794130 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749700 | GCCTCCCAGGTTCAC[A/G]CCATTGTCCTGCCTC | 5521 |
rs371795981 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029536 | AATTATTGATGCTTT[A/G]TAAGATATCTTAATA | 5521 |
rs371796228 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991973 | ACAGAGTCCATGGAA[A/T]CCATATCAAAATTCC | 5521 |
rs371798072 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803874 | ATCAGGTAATAATTA[C/T]ATAGTTAAGCTGGTT | 5521 |
rs371831835 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623799 | GATAATGATGGAAGG[C/T]CAGCAGGTGCTTTGA | 5521 |
rs371834279 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075481 | GCCTCCTCAGGTTCT[A/G]TCTCTATCTCTGAGA | 5521 |
rs371835457 | in-del | -/TTCT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955766 | TAACAATAGTCTTCT[-/TTCT]ATTACTTTTTTTTTT | 5521 |
rs371849293 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976295 | GGCATGCACCACTAC[A/G]CCCAACTAATTTTTG | 5521 |
rs371849370 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591654 | CGACTTATTTTTAAA[C/T]AAGTAAGAGATTATT | 5521 |
rs371851617 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986527 | GTAAAACACAGAGAA[A/G]CAATTCAGAAATTTA | 5521 |
rs371851678 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999288 | TAAAGAGGATGATAC[C/T]AAGGAAGGTGGTAAA | 5521 |
rs371853618 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744567 | TCCTACCCTCACATG[C/T]GTCACCAGGGAACCA | 5521 |
rs371859052 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960643 | ACCATTAGACCTGCA[C/T]GAAAATGGACCAAGC | 5521 |
rs371862948 | snp | G/T | 1.74601e-05 | 0.00295461 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650767 | CAGAACCAAAGATCT[G/T]CCATAGGAAAAGAGT | 5521 |
rs371867441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817395 | CACCACCACCATTTT[A/T]AAAACTTTGATGATA | 5521 |
rs371883329 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628007 | TGGAGTGCAGTGGCA[A/C]AATCTCAGCTCACCG | 5521 |
rs371890136 | snp | A/G | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861427 | CAATCTCCTGACCTC[A/G]TGATCCACCCAGCTC | 5521 |
rs371908167 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655345 | GGAAGCTCTTCCCCC[C/G]CAGAGAGTGGCACGG | 5521 |
rs371908970 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715183 | GTAAATGGCCAGACC[C/G]AGGTGATGGTGCCAG | 5521 |
rs371909113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743958 | TATTTCCCACTGAGA[C/G]AGAATCACAGGTTAG | 5521 |
rs371912584 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036196 | AACAGACCCCAGTGT[C/G]TGTTGTTCCCCCAAT | 5521 |
rs371919406 | snp | C/T | 0.180064 | 0.240019 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609735 | GAAAGGGGTGACGGA[C/T]GCACCTGGAAAATCG | 5521 |
rs371928200 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623240 | GGTACACATAGGATA[C/T]GCTGAGGATAAGAAC | 5521 |
rs371929797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651421 | TACATAAATACTTCT[C/T]AGTAAGTATTTGTTG | 5521 |
rs371937303 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747829 | TTAAGTAGTTTGAAC[C/G]TAACTACTTAGTAAA | 5521 |
rs371940465 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631038 | AGTCCCTGAATTCAC[A/T]CACTACTGTCAGTTT | 5521 |
rs371944999 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060647 | AAAAAAAAGAAACAA[A/C]AAAAAAACAAAACAA | 5521 |
rs371953856 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070226 | CTATTTTGAGGGCTT[C/T]TGTGTTTTCAACACC | 5521 |
rs371954169 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022852 | AGTCTAGATAGAACC[A/G]GTGAAAATATTCTTA | 5521 |
rs371955775 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903811 | GAAAGTTAAAGTTGT[A/G]TCAGAATACTCAGTT | 5521 |
rs371958366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703225 | GGTACAGCCTAAAGC[A/G]GGCATGTCTATTGCT | 5521 |
rs371987361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619412 | TTGAACCTGGTAGGC[A/G]GAGATTGCACTCCAG | 5521 |
rs371997913 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590394 | CTTTTTGTTTTTTTT[G/T]TGTGTTTTTTTTTTT | 5521 |
rs371998334 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659288 | TCTGCAATTATTTAA[C/T]ATTACAATGGAAATG | 5521 |
rs372005387 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672414 | TGCTCAGGGAAGGGG[C/T]TCAAAGGGTTTCTGT | 5521 |
rs372013137 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646712 | AGACAATCCAGATAA[C/T]AAAATTAGCAGAATA | 5521 |
rs372016894 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082315 | CTGATGGAAGTAGTA[C/T]AGAGTCATCATTAAA | 5521 |
rs372035007 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768543 | TCTCTCCATTCACCT[C/T]CTGCTTATTTTGCAT | 5521 |
rs372043052 | in-del | -/GAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781022 | TCAGATGATGATGAT[-/GAT]ATTAGTTAATACAGT | 5521 |
rs372048538 | in-del | -/ATAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687022 | TGTGTAAGTGTGTGT[-/ATAT]GTATGTGTGTGTGTG | 5521 |
rs372048942 | in-del | -/AAG | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023064 | TTAATTTTTTTAAAA[-/AAG]AATAACAATGAATTG | 5521 |
rs372048999 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973923 | AAGCCTATAGGGTAA[A/G]GGATCCTTGTTCCCC | 5521 |
rs372050455 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038982 | TAAACACAACTGCAA[A/C]CCCCACCATGAAAAG | 5521 |
rs372056458 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013927 | GCACAGCAAAAGAAA[C/T]TACCATCAGAATGAA | 5521 |
rs372059352 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645975 | CTCTTTGCCAAGTTA[A/G]TTCATAGTCTTCCTC | 5521 |
rs372060576 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813510 | AATCAGTGTGTCGCT[C/T]GGTTCCATGGAGACA | 5521 |
rs372068033 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888559 | CAGAATGGTCCTTTT[A/G]AATGCAAATCACTTC | 5521 |
rs372080666 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710972 | CATATTTTGGGACTG[-/G]CTCAGGTATCACTTC | 5521 |
rs372085168 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068032 | TAGTAAACACATGGA[A/T]CTGATGGCCATTTTA | 5521 |
rs372097265 | snp | C/T | 0.177824 | 0.239355 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615425 | CGTTAGTGGGTGCAG[C/T]GCACCAGCATGGCAC | 5521 |
rs372098445 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829531 | ACAGATAAGGTGGGG[-/G]CTGTGATGGGGAGCA | 5521 |
rs372102299 | in-del | -/CACACACACACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740574 | ATTTTAAAATGAGAT[-/CACACACACACACA]CACACACACACACAC | 5521 |
rs372118507 | snp | C/T | 0.000435635 | 0.0147522 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147055787 | AAAAAAACAGTCTCC[C/T]GAATCCATAAGGATT | 5521 |
rs372121740 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642645 | TGAGCTAAATGGGAA[A/G]ACACTAAAACATTAG | 5521 |
rs372129488 | snp | A/G | 3.34863e-05 | 0.0040917 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600269 | ATGTTCAATATACCT[A/G]TGGGTGCCTGGGGTT | 5521 |
rs372144875 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619211 | GGACTGTGGCAAACT[A/G]GAGTGTCCACACCCT | 5521 |
rs372152202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010044 | CAAAGTGAGGTGTGC[A/G]TACTCATAAATACAC | 5521 |
rs372164556 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969606 | ATCCAGGAGCGAGAT[A/G]CAGGTTGCCTGCCTG | 5521 |
rs372171957 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970978 | CTTTTGATCTATGCA[G/T]AGAAAAACAGAGATC | 5521 |
rs372172277 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998729 | TAAACTCTTCTTTCA[A/G]AAGAAATTAACCAGA | 5521 |
rs372176428 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014691 | AATTGAACAATGAGA[A/T]CACATGGACACAGGA | 5521 |
rs372178938 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930943 | TTTTAACTTGCAAAA[G/T]CTTAATTGCTCACCA | 5521 |
rs372180638 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598862 | TCCTCCCCAGCACAA[-/C]CAGAATGTTCATTTA | 5521 |
rs372182597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932343 | AATCTCATCTTGAAT[G/T]GTAGTTCCCATAATC | 5521 |
rs372187518 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007964 | CAATTCCGGACACAA[C/T]AGTCCATAAGGTTAA | 5521 |
rs372188437 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981560 | TGTGGGTTCATAAGC[A/G]CTTGAAAGAAATAAT | 5521 |
rs372189344 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696256 | CTACAGGTGCCGGCC[A/G]CCACACCCGGCTAAT | 5521 |
rs372191024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904780 | GTCAAAATGAGGGCA[C/T]GGACATGGTACTGGA | 5521 |
rs372191101 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938751 | TGGTTAGATAATAGC[A/C]TTTTTTTTTTTTTTT | 5521 |
rs372191763 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729207 | TCTTGTTATGTTTTA[C/G]CAAAGAGACTGGTGG | 5521 |
rs372192718 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916630 | ATTGACTTCCCTCAT[C/T]CATCTGAGTGAGTCC | 5521 |
rs372198638 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905149 | ACTAACTATGTCAAG[A/T]GTTGGTGAGGACATG | 5521 |
rs372202174 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011045 | CAAAATCCTTGCCAC[A/G]CTCCCTTCCTGTGAC | 5521 |
rs372204083 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042110 | CAAATCCCCACGTCT[A/T]TCACCTTGTAATAGT | 5521 |
rs372207203 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680451 | CCTAATGCTAGATGA[C/T]GAGTTAGTGGGTGCA | 5521 |
rs372219228 | snp | C/T | 1.65007e-05 | 0.00287229 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701021 | AGTGAAGAAAATGGG[C/T]ATTTTGCATTCACCA | 5521 |
rs372230649 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881809 | TGAATAAATTGCTGA[A/C]TATCTTACTTTAATA | 5521 |
rs372236948 | in-del | A/CC | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864816 | TCTGATCTTCACCCC[A/CC]CATAAGTTTCCTAGG | 5521 |
rs372251318 | in-del | -/ATT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854408 | CCTTGAGTATTTATT[-/ATT]TCTATGTGTTGGGGA | 5521 |
rs372257452 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905522 | GACCTCCCAAAATGT[G/T]GGGATTAAAGACATG | 5521 |
rs372268742 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909821 | TTGCACAATATTATT[A/G]ATAATTCAATCATAC | 5521 |
rs372279505 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762375 | GAAGAAAATAGTACC[A/G]AAAGCTGCACAGAAG | 5521 |
rs372289889 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810797 | GTTACATATGTATAC[A/G]TGTGCCATGTTGGTG | 5521 |
rs372300421 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882501 | CAAGTTACAAGATCT[A/C]CCTAAAGCATCATTT | 5521 |
rs372308055 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836987 | GGTTTTAGGTGCTAC[A/G]CCAACAACTAGCAGC | 5521 |
rs372321267 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060600 | ACCACAGCACTCCAG[A/C]CTTGGTGACAAAGTA | 5521 |
rs372322880 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603775 | AAAACAGCCTATGAA[A/G]TAGGAATTATGATTC | 5521 |
rs372323175 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673636 | AGGAAGATTCAAAAC[C/T]AAGACCCTTGACTTT | 5521 |
rs372327262 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867674 | CACTTCGGCCACCTC[A/G]TGATAACAGAGAGAT | 5521 |
rs372336671 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938570 | AAATCAGGTAATAAA[A/G]TATTTGTTATAAAAT | 5521 |
rs372338442 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888285 | TCACAGGGTATAAGG[C/G]ATCTCAATCCCTAAT | 5521 |
rs372342853 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972950 | ATTTCTTATTTTTTC[A/T]GTTGTGTTTTTGCCA | 5521 |
rs372349062 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950368 | AAATGAATAGCTTTG[C/G]TGATATCACTGCCAA | 5521 |
rs372359521 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636249 | GTATATATCCTTGGG[A/C]GTTAGGAAGAGGGGA | 5521 |
rs372370672 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826048 | TGTAGAAGCTGTAAA[A/G]TTTATATCCGGTAAA | 5521 |
rs372383737 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659695 | TACTAAGATCATTGT[C/T]ATTTTATGGATGTAA | 5521 |
rs372394689 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689964 | CACAGAGTCTATATT[C/T]AAAAAGTAACTGCTG | 5521 |
rs372400540 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755722 | AAGGTTATGGAAAAG[A/G]TATTTTAAAAGTAAA | 5521 |
rs372402821 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759929 | ATGATATTGTAATAC[A/C]CTATTGGCACATCAT | 5521 |
rs372403613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761106 | TGGAAGTCAGTGTGG[C/T]GATTCCTCAGGGATC | 5521 |
rs372408691 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731316 | TGCTGGGTACCTGAT[A/G]TTTGCTGCAGCCTCA | 5521 |
rs372413642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784458 | CAACACAACATTCCT[C/T]GGGATTATTAGATAT | 5521 |
rs372416836 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823279 | CTCGACTCACTGCAA[C/T]CTCCACCTCCCAGGT | 5521 |
rs372419333 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799425 | TAGGGTTTCTCAGCT[G/T]CTGGCTGCTGGAAGA | 5521 |
rs372419823 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907997 | GAAAAACTGCCGAGC[A/G]GAACAGCAGCAGCAA | 5521 |
rs372446157 | in-del | -/CTCTCT | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617694 | CATCTCTCTCTCTCT[-/CTCTCT]TTTTTTTTTTTTTGA | 5521 |
rs372447772 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869142 | ATGAATAGGTAGATC[A/G]GGTATTCTCATTCTC | 5521 |
rs372451824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685974 | TAATAAAACATTCCT[G/T]CCCCATGGTCAGGAA | 5521 |
rs372453445 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740991 | GCAGTGAGCTGAGAT[C/T]GTGCCACCGCACTCT | 5521 |
rs372457698 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920612 | ACTGCCAGTCCCTGC[C/T]AGGAAGTGGCTTTTC | 5521 |
rs372463073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781891 | TGTGTCACCACCAAA[C/T]CTCATGTTGAATTGC | 5521 |
rs372465991 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994689 | TCTGCCTCCAAGACC[C/T]GCTCTGCCCAACACT | 5521 |
rs372466920 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678232 | GGGATGCAAGGCTGG[C/T]TCAATATACGCAAAT | 5521 |
rs372467255 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147081425 | TCAGGCCCTGGCAGC[A/G]TCCTGGAGTGGTTAC | 5521 |
rs372471793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043164 | GCTGAACTCCTGAAG[A/G]CAACCTAAAATAGGT | 5521 |
rs372486810 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055184 | CAAGTACAGACTCCA[A/C]GTGAACCAATCCAAC | 5521 |
rs372491520 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005034 | GTTTATGGCTATCAG[A/G]CAGCTGCCTACTTAG | 5521 |
rs372500318 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966199 | GTGTTGGCCAGAGGC[G/T]CGTTAATGTTGTCAT | 5521 |
rs372507515 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951340 | TCCCCGTTTAAAGTT[C/T]CTCATGCCTTTTTTT | 5521 |
rs372510154 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678553 | GCCAGGGCAATTAGG[A/C]AGGAGAAGGAAATAA | 5521 |
rs372515064 | snp | C/T | 4.94645e-05 | 0.00497291 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600371 | TGGTCATGATATACC[C/T]CCCACTGTGGCTGAA | 5521 |
rs372523396 | in-del | -/TA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719218 | TCTCTGCCCCCTACT[-/TA]TTTAATCTGCAAAAT | 5521 |
rs372530454 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146891368 | ACACCCAATAAATGT[C/T]TGCTCTTGGTATTAG | 5521 |
rs372551969 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595273 | CTCTGCTATAAACTA[A/T]CTCATTCACCTTCAC | 5521 |
rs372576953 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764266 | AAAGCCTTGTGGGCC[A/C]ACTTTTGAAGGAATT | 5521 |
rs372581670 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593076 | ACCTGGAGAGGAAAC[A/G]TATCGAGAAGGTCAG | 5521 |
rs372611320 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884090 | TATGTAAATTCAGGG[-/T]TTTTTTTTTTTTTTT | 5521 |
rs372617336 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991475 | TAGGTACAACATTAC[A/C]TTAGGCAGAAATAAT | 5521 |
rs372618405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065601 | CCAATATCCAGAGAA[A/G]AGAAGATGGTGTCCA | 5521 |
rs372621800 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616302 | AGAAAACACTGGGGA[A/G]AGTCTCCAGGACATT | 5521 |
rs372629685 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983469 | ATAGGCGTGAGCCAC[C/T]GCACCCGGCCCAGAG | 5521 |
rs372629698 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008468 | GCTGTCTTTCCTCAT[G/T]CCTGCTACTGATCAC | 5521 |
rs372643676 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644389 | AAGTTAAAACTGTGA[C/T]GCGAATCCAATGTAT | 5521 |
rs372650307 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916199 | AATGCAAAGGGTTAG[A/T]ACTTTTAAAAGGCAT | 5521 |
rs372655758 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838721 | AGTGATATGCTAACA[A/C]ATTAATGATTAATAG | 5521 |
rs372664243 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856348 | TAAATTAACTTGTGT[C/T]CTACGGAACAAATTT | 5521 |
rs372664818 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652775 | ACCCCCCCCCAAAAA[G/T]TTTTGCCATTATTCC | 5521 |
rs372666923 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917387 | CATTATCTATGTTTG[C/T]GCTTTTGTCACCAAG | 5521 |
rs372675663 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873125 | TCCGCTTTTAGTGAT[A/G]CGCCCCATTATGCAT | 5521 |
rs372712525 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669416 | AGTTACTAAGGTTTA[A/C]GGAAGTATATTTTTC | 5521 |
rs372716254 | in-del | -/CATCCCAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909872 | TTTCTACCATCCCAC[-/CATCCCAC]AAAAAAGCCCAAACA | 5521 |
rs372724252 | in-del | -/GA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753357 | TCTCCCACACACAGA[-/GA]ATAGACAGTATAGAA | 5521 |
rs372747470 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772407 | ATATATATATATATA[C/T]ATATATATATATATA | 5521 |
rs372749053 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800813 | CCAAGAGAGATCCAC[A/G]TTCTCATGCTCATTG | 5521 |
rs372757082 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998946 | GGGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 5521 |
rs372770392 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811016 | GCCGAGAATGATGGT[A/T]TTTAGATGGAGTCTT | 5521 |
rs372776903 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826958 | TTATGTTTTCAACCT[C/T]ACTGGAACACTAGCT | 5521 |
rs372785404 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147028973 | TTTTGAAATGCCTGT[C/T]AAGTCTCTTGCCTAT | 5521 |
rs372798271 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775915 | GCTTAGGAATAAATT[G/T]AACTAAGGAGGTACA | 5521 |
rs372799154 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038074 | ATACTTTTAGAACCA[A/C]GGTTCTTTGACCCAT | 5521 |
rs372810731 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014412 | AATGACTATAAATCA[G/T]GCTGCTATAAAGACA | 5521 |
rs372819794 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948711 | TCATTCATTTGGTGC[-/A]AAAAACTTCTATTAA | 5521 |
rs372833433 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853302 | GTGATTCATGCCCCA[A/G]TTTAAAATGCATAAT | 5521 |
rs372837306 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049028 | AGGAAAAATAAATAG[A/G]GTAAAACTAGCTGGG | 5521 |
rs372853359 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686728 | CTAGGTTCCCAGGGC[A/G]CTGGCAGCTGATAAT | 5521 |
rs372857165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005785 | GGAGTCAGAAAGAGA[A/G]AAAGAGAGAGACAGA | 5521 |
rs372868714 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786510 | GGCCTCCTGACAACC[A/T]CCAACTATCACTGAA | 5521 |
rs372874499 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054359 | TCCATGCCATTTTTT[C/T]ATTCCTCTCATCCCC | 5521 |
rs372882373 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734016 | TAAGTGCTTTACATA[C/T]ATTACCTCATAGGGT | 5521 |
rs372887103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810337 | GAAGACAATGAGAGC[C/T]GAGTGAAAGGAGTTT | 5521 |
rs372890754 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721697 | CAGTGATCATTAAGG[A/C/T]GAAACATTTACAGAA | 5521 |
rs372894587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963533 | ACTTAATTGAACATA[C/T]TGTGTTAGTTGAGCA | 5521 |
rs372913966 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825228 | AACCCTTCAGAGGGT[C/T]GCTGAGCTGTCCATG | 5521 |
rs372919692 | in-del | -/AA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040823 | TAAAAAAAAAAAAAA[-/AA]CTGTAAAATAATAGT | 5521 |
rs372920750 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960359 | CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC | 5521 |
rs372924644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934023 | AACTCATCGTTTTTT[A/G]TGGCTGCATAGTATT | 5521 |
rs372926895 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778057 | GAGTTTAAAGTTCTA[C/T]GAGAATTGTGTACAA | 5521 |
rs372947421 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770127 | TGAGGTCAGCAGTTC[A/G]AGACCAGCCTGGCCA | 5521 |
rs372958718 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961653 | GATGCCTTTTATATG[C/T]TAAGAGTATTAACCC | 5521 |
rs372967926 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893112 | TCACTCATCCATCCA[C/T]TTATTCCCTCGTGAT | 5521 |
rs372999066 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060205 | TCAAATCCCCCTCTT[A/T]CAGACTCCCACATAC | 5521 |
rs373007831 | in-del | -/ACAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979559 | TCTTCCCACCTTGAA[-/ACAC]ACACACACACACACA | 5521 |
rs373010727 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683043 | ATGGCCAAGAATATG[-/G]CCGAGAAATACGGGT | 5521 |
rs373014349 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714153 | AGAAAATCAAAGAAA[A/C/T]GTAATGTCCTGGAAA | 5521 |
rs373031245 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848968 | ATTGTTCCACTTTGG[A/C]CATTAGGAGCTCTTC | 5521 |
rs373041531 | in-del | -/G | 0.0039928 | 0.0445023 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838581 | TCTCAAAAAAAAAAA[-/G]AAAGAAAAAAAAGAA | 5521 |
rs373046049 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789768 | GTGGTCAGGGCTGAC[A/C]TCTCTGAGGAGTGAC | 5521 |
rs373048543 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016640 | GGTGCTATGGGAACA[C/G]AAAGGCAGTATATTC | 5521 |
rs373049997 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031270 | TTGCTTTTATCTTAA[A/G]GGTTATTTTATTAGA | 5521 |
rs373053307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828336 | TCCATTTAACATCAT[A/G]AAAGAGAAACTTCTG | 5521 |
rs373056171 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993309 | GTGCAGTGACACCAT[A/G]TTGGCTCACTGCAGC | 5521 |
rs373058227 | in-del | -/CT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788829 | CAGAAACAAAACTCT[-/CT]GCCTTGGGGTTTTGA | 5521 |
rs373076820 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632116 | CCAGTACTGCAAAAT[A/G]TAACTGTATTTGGAG | 5521 |
rs373077541 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596242 | AAAAACTTGAAAATA[C/G]CTAATCATACTTAAG | 5521 |
rs373091238 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960493 | GCGGGTTTCACCATG[C/T]TGGTCAGGCTGGTCT | 5521 |
rs373094486 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001463 | TTCACTCCTGAAGTC[A/G]GCAAGACCACAAACC | 5521 |
rs373098127 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852927 | AAAGTGCAATTAGAG[C/T]TTTGGATTATCAGCA | 5521 |
rs373099782 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807776 | CTCCTGGGGTGCCTT[C/T]TTTTTTTTTTTTTTT | 5521 |
rs373100302 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655440 | CATCCCACCTCAAAT[C/T]GCACAGCCTTCAGTC | 5521 |
rs373101696 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888426 | TACTCACCATCTCCA[C/T]TGCTGCTACCATGCT | 5521 |
rs373112657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050580 | CATTTAACAGCTGTG[C/T]GAACTTAGACTACTT | 5521 |
rs373127628 | snp | A/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589927 | CAGTATGTGAGATTA[A/T]TAAGTAATAACTTGT | 5521 |
rs373139839 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021036 | AACAGAAGTGGAGTT[A/G]AAACAATACTTTTTT | 5521 |
rs373143287 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619989 | ATTGGCCCCACAGAA[A/G]GGCAACACCAGTGAC | 5521 |
rs373148009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639289 | CCAGTTGGAAAGTTT[C/T]AGGGTCCCGTGGAAA | 5521 |
rs373163398 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977655 | CCTGTGTTAGTTTGC[A/C/T]GAGAATGATGGTCTC | 5521 |
rs373164979 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670818 | ATTTTCTTTAAACTG[-/A]TTTGCTTTTAGTTAA | 5521 |
rs373166993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820014 | TATGTGGAATCTAAA[A/C]ATGTTGATCTCAGAG | 5521 |
rs373197900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596761 | GCCAAGCCCTGAAGT[C/T]GAGGTAGGATTCAGG | 5521 |
rs373198023 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646846 | TACCCTAAATGTGTG[C/T]GTGCGTATGTGTGTG | 5521 |
rs373201878 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727576 | CTATCAGGTAGAATG[C/T]ACTCTATTTAGATAG | 5521 |
rs373205379 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858314 | CCAGTGCAAATAATA[C/T]TTATGACCACTTAAG | 5521 |
rs373212667 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912194 | CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA | 5521 |
rs373212675 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691744 | GACCCCCCTGTCCAT[C/T]CTCTCCCTGCTCACT | 5521 |
rs373226291 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906471 | GGGATTACAGGCATG[C/T]GCCACCACGCCCAGC | 5521 |
rs373237904 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078226 | ATAGCTTACAAATAT[C/T]GAGTACTTACAAAGT | 5521 |
rs373239591 | snp | C/G | 3.32055e-05 | 0.00407451 | intron-variant, missense | PPP2R2B | GRCh38.p7 | 5:147055689 | GGCAGCTGGAAGAAA[C/G]GATGGTGTTCGGAGG | 5521 |
rs373264063 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608424 | CTTATCTTGTTAAGA[C/T]GCAACTTATCTTTAA | 5521 |
rs373277435 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594836 | AGGAGATAGAACTGT[A/G]TGAAAGCAGAGGGAG | 5521 |
rs373291805 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940681 | TAGAATTGGGTTTCC[A/G]TCATTTGAAACTGCC | 5521 |
rs373292222 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146800736 | CAGCTGTGCTTGGAT[A/G]GGGTAGGAATGACTA | 5521 |
rs373299569 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708395 | TCTGTATATCTATGT[A/G]TGTGTGTGTGTATGT | 5521 |
rs373301224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910545 | ATCTCTGACCATTAG[C/T]TGCCTCATCTGCAAA | 5521 |
rs373310132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992347 | TCACTGGATATCAGA[C/T]TGTAGTTCTCTTTCA | 5521 |
rs373329397 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953195 | ACTGATTGTGAATAA[A/G]TCTGCAACATGGCTT | 5521 |
rs373330286 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032452 | GAGATTTTGGTTCAC[C/G]TATCACCCAAGCAGT | 5521 |
rs373337193 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910253 | TTAGAATTTCAAAAA[-/A]TTTTGCAGATAGAAA | 5521 |
rs373341259 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687025 | TGTAAGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 5521 |
rs373348657 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050690 | CACACACACACACAC[A/G]CATCCATACCTACAT | 5521 |
rs373350946 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844277 | GTTAGTGGGTGCAGC[A/G]CACCAGCATGGCACA | 5521 |
rs373378552 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807590 | CAGCCCTGGGAGTAG[G/T]TTCTATTGTTATGTT | 5521 |
rs373386906 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055017 | CATGCTAGGTTAGAA[G/T]GCAGCAGAGAAGGTC | 5521 |
rs373393176 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882044 | GCACTTTGGGAGGCT[G/T]AGTCAGGCAGATTAT | 5521 |
rs373401517 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949784 | CCATCAACAGATGAA[G/T]AAAGAAAACATGGTA | 5521 |
rs373420073 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892257 | TAGAACTATGAGCAA[A/G]TTCTCTTAACTTTTC | 5521 |
rs373420137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653777 | ATTCCATGATGTACT[A/T]CTTAATGGGGAAGGG | 5521 |
rs373421681 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999648 | ATAAACAGAAGCAAA[A/C]TGATTCATCTCCCAG | 5521 |
rs373423208 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932794 | ATTTGTGATCATGAT[A/G]AACAAGGTCAAAGAG | 5521 |
rs373434857 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983382 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 5521 |
rs373440818 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843945 | TAGCAGCATGATTTA[C/T]AGTCCTTTGTGTATA | 5521 |
rs373444509 | snp | G/T | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589998 | TGTAGCCGCCACTGC[G/T]ATAATATTTTCTGAA | 5521 |
rs373449908 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870669 | TCCCACAGGTAAGGT[A/T]CTCTTCGCCACGCTC | 5521 |
rs373458169 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885161 | TGGAAAGGGTTTTAC[G/T]TGCATTGTCTCATTT | 5521 |
rs373481273 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823145 | GATTTCATCTGACAG[C/T]CTGCATATCACTACC | 5521 |
rs373496033 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909664 | TCAGCTTGCAGCTGC[C/T]ACTGTGTTGCAAGCC | 5521 |
rs373503818 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995660 | TGTCTTTTGATGACT[G/T]AGAAGAAAATTCTAT | 5521 |
rs373536063 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765094 | TGACAAATGTATCTT[C/G]TTTTTTAAGTTCCAA | 5521 |
rs373558208 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844876 | TTTACCTTTAGCCTA[A/C]ACAGTGACCTGAGGT | 5521 |
rs373562409 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907889 | GCAGTGGTTTGTTAG[C/T]CTTTCAAACTGGCTG | 5521 |
rs373571917 | snp | A/G | 4.98326e-05 | 0.00499138 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650602 | CCTCAGGTCATCAGC[A/G]GACATGTAGGTTTCA | 5521 |
rs373576739 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890956 | CTATTTCACAGATAG[-/G]AAGAAAAAGAGAGAG | 5521 |
rs373583934 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758929 | CTCTTACATGGAATT[A/T]TTTTTTTCCCAAATG | 5521 |
rs373584414 | snp | A/G | 0.000169986 | 0.00921758 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856450 | CTATTTAACACTTCT[A/G]TACTGCTACTTTATC | 5521 |
rs373591436 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684453 | GACAGACAGAACGTG[C/T]TTCATTCCCAGTTCT | 5521 |
rs373595472 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659472 | GGCCTTGGGTTTGCT[C/G]CTTAGTCTTTCTTGA | 5521 |
rs373600568 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615708 | TAAAAGGTCTCTACA[A/G]TGAAAATTAAAAAAC | 5521 |
rs373602934 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038935 | TATAATGAAGTAGGA[G/T]GGCTTAAGTATTTGA | 5521 |
rs373603528 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878923 | CACCTGGGCAGCAAG[C/T]GACTAGCTTGCAGGT | 5521 |
rs373615570 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637362 | TTATTGGCATCTAGT[A/G]GGTAAGGCCACAGAT | 5521 |
rs373620943 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959261 | TCTAGCATTAATGTT[A/T]TCATTCAATTGTTTA | 5521 |
rs373629962 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661088 | GCCATAAGCATTCAA[A/T]CCTCTAAATCAGTGT | 5521 |
rs373632437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009319 | ATTTTCCTAATTTTA[C/T]TTACTTTTTAGTCTC | 5521 |
rs373639616 | snp | A/C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969405 | CATCAGATAAAATTG[A/C/G]GGGGAGGAGAGTACA | 5521 |
rs373644854 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601107 | CATCCATGTCGTAGC[A/C]TGTATCAGGTCTTCA | 5521 |
rs373665353 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606269 | TTACACTGGACCTTC[A/C]TTAATTTCACAGGAA | 5521 |
rs373666695 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635398 | GCCTAGTACCAATTA[A/G]TTATTTACCATTCTA | 5521 |
rs373679856 | snp | A/T | | | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146650615 | GCGGACATGTAGGTT[A/T]CATAGTCGCTGTTGA | 5521 |
rs373680855 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836170 | CTACTATGCCCTCCC[C/T]ATGCAGCTGCCAACA | 5521 |
rs373694037 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927304 | AAGTCCACTCTTTGC[A/C]TTGGGTTTTGACTCG | 5521 |
rs373704447 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956313 | CATGAATGGAAAAAA[C/T]TTTGCCTGAATTCTT | 5521 |
rs373705844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892609 | CACTAAGTCAGTATG[A/G]TCTTTCTAACTTATG | 5521 |
rs373716062 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648213 | ACTTGTGATCTTCCA[C/T]GACCTTCCCCTTTTA | 5521 |
rs373724077 | snp | A/G | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919086 | TAGATGAGGAAACAG[A/G]TTAAGAGGAGTTAAA | 5521 |
rs373740293 | in-del | -/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590386 | ATTATTGGCTTTTTG[-/T]TTTTTTTTTGTGTTT | 5521 |
rs373746389 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927802 | GCAGTGGTGTGATCT[C/T]GGCTGACTGCAACCT | 5521 |
rs373748887 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966496 | GCAGAGCCAAAGATC[A/G]GCCTCCTCTGACATG | 5521 |
rs373765820 | snp | C/T | 1.69905e-05 | 0.00291461 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697976 | AACAGGAATTCCACC[C/T]ACCATTAGTAGACAG | 5521 |
rs373772556 | snp | C/T | 1.65509e-05 | 0.00287666 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878063 | GCGGGTATCAATGTC[C/T]TCCTCCATTGACAGC | 5521 |
rs373774918 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918251 | GAAGGGAAACTCGCC[C/T]TGGGCTCTGCACTAC | 5521 |
rs373783401 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848428 | GTCATGGCTCCTCAG[G/T]CTCCTTGAGGCTGTG | 5521 |
rs373784760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691318 | CCTGGGGGCAATGGG[A/G]AGAGGAAGAGGTAAG | 5521 |
rs373791052 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844210 | GACTGTGGTGGGGTC[A/G]GGGGAGGGGGGCGGG | 5521 |
rs373793295 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865730 | GTCAAACATTCATTC[C/T]ATTACATCTCTAATC | 5521 |
rs373796137 | in-del | -/TG/TGTGCG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808995 | gtgtgtgtgtgtgtg[-/TG/TGTGCG]CGCGCGCACCCACTT | 5521 |
rs373804502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060468 | CCCACCTCTAAAAAA[C/T]ATACAGAAAATTATC | 5521 |
rs373810764 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953285 | TACACATATACTTAC[A/C]CAGACATATTTATAT | 5521 |
rs373814921 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808520 | ACTAAGAGGTAAGAG[-/G]CTGTCTGGAAAGGAA | 5521 |
rs373817744 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021868 | CAAACTCTAAAAATG[A/G]TAAGGATGATGGATG | 5521 |
rs373827416 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005305 | CATAGTTAGTGATGT[-/A]AACATACTTGAAAGT | 5521 |
rs373829916 | snp | A/C/T | 8.92091e-05 | 0.00667814 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590230 | GTCATGATGACACTG[A/C/T]AAGGCAGAGAGCAAA | 5521 |
rs373832384 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908659 | TGTAGTTGAAGAAGG[C/T]GATGACCTAGAGTGT | 5521 |
rs373840145 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794776 | GAAAACAGCCCTTAT[G/T]AATTGTCTCTATTTT | 5521 |
rs373844035 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882148 | CAGGCATGGTGGCAC[A/G]CGCCTGTAGTCCCAG | 5521 |
rs373847206 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897018 | ACTGAGCATATATTT[A/G]TCATCTCCTTTTCCC | 5521 |
rs373853473 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704838 | ACTTAACAATGATAC[A/G]CATGTGAGGCTAATG | 5521 |
rs373858347 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056457 | ACTACTGCCTCTTTC[G/T]TCCCCTGCCAGCCTT | 5521 |
rs373862325 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831642 | TAAAAAAGCATCAGG[A/T]TAGCCAGGCGTGGTG | 5521 |
rs373864080 | in-del | -/ATATACGATCCTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834716 | GTGTGTTGAGACTTG[-/ATATACGATCCTG]TCACCCAAGTAGTGA | 5521 |
rs373869032 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033588 | TGGGAAGGTTTTAGG[C/G]GGTTTGGGATGGAGA | 5521 |
rs373880872 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030402 | CTTTCATATTTTCTA[C/T]GAAAATATCCCATTA | 5521 |
rs373882517 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898677 | GAAACTACCATCAGA[A/G]TGAACAGGCAACCTA | 5521 |
rs373910831 | in-del | -/GGGGG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071590 | GCAATTGTACTGGCT[-/GGGGG]GTTCCCTCTATCTGG | 5521 |
rs373916534 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051627 | TTTAGGAAAAGAAAG[C/T]GTCCCTACTGATTTC | 5521 |
rs373923755 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715287 | TTCCTTTCCTGCAGT[A/G]TGACTACAGGTAGAG | 5521 |
rs373924694 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729264 | TGAAACTTTGAACTT[C/G]AGAGAGATGATTTAG | 5521 |
rs373952760 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886752 | TAGTTTTCTTTTGTG[C/T]TCATGTTTTCGTTAA | 5521 |
rs373960607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795758 | ATAGTATATCAAAAC[A/G]TCAGGTTGTGCAACT | 5521 |
rs373961926 | in-del | -/TTCTTTTTTTTTTTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807774 | ACCTCCTGGGGTGCC[-/TTCTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 5521 |
rs373964720 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771421 | TTGTGCTGTCAGTCA[C/T]TTTCAGATCAACTAC | 5521 |
rs373965135 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990485 | GAAAAAACAGTCCCA[A/G]TAAATGGTGGTGGAA | 5521 |
rs373966061 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821274 | TCCCTTAATACCATA[C/T]TCTTCTCTCCCATTT | 5521 |
rs373971324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814644 | TCCCTCTGGAACACT[A/G]GATTGGTAAGGGGAA | 5521 |
rs373972286 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855626 | TTTATTAAAGGGAGC[G/T]CTTCTCTTCTGAATG | 5521 |
rs373987715 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764448 | TACACAAGTCTATTG[A/C]CTCTTCTGGATGGCT | 5521 |
rs373988234 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843187 | GCGAAACTCTGCCTC[-/A]AAAAAAACTTTAAAA | 5521 |
rs373988506 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808197 | GGTTTGTGCCGTCCA[A/G]TGGGTTAATCAGTAG | 5521 |
rs373989652 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729103 | ATGGCTGTGTCCAAA[-/A]TGCTGATAGCGATAT | 5521 |
rs373992116 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929394 | CGAACAAGTCAGCAG[C/T]GGTTCTATGGTTCTG | 5521 |
rs373998486 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639559 | CAGAGGGGCCGAGGT[A/G]CTGTCTGAGGACCCA | 5521 |
rs373999873 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014166 | GCCATCAGAGAAATG[C/T]AAATCAAAACCACAA | 5521 |
rs374002867 | snp | C/T | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923868 | AATATGGTACATATA[C/T]ACCGTGGACTACTAT | 5521 |
rs374012991 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717169 | ATAGGCTTATAGCCT[G/T]GGACACCTCTGAAAT | 5521 |
rs374014915 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693027 | GGTTTGGAATCAGAC[A/C]ACCTTGGGCCCAATC | 5521 |
rs374022902 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738055 | CACTCTCAGTGTGGT[A/T]TGGAAGATATGCCAT | 5521 |
rs374028515 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773374 | CATCTTTTCAAAAGG[C/T]TTGCACAAAGCAGAG | 5521 |
rs374028922 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693896 | ATGTCAGCACATCCT[A/G]TTTCTTATCTGTAAC | 5521 |
rs374036807 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935277 | TCATTCCTTCCATCA[A/T]GTGAGGTACAGCTAG | 5521 |
rs374039647 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601629 | ACTTGTTGTGTGACC[A/T]TAGGCAAGATACTTC | 5521 |
rs374046567 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737755 | GGTGGGTGTCACGGT[C/T]TTCTTTGAGTGTATT | 5521 |
rs374046956 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833760 | CCCATCCTCCTCCCC[C/G]ACCCCCAGCTGCACA | 5521 |
rs374047241 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849929 | GGAGGATCACTCCAA[C/T]AGCACAGCAGAAAAA | 5521 |
rs374050985 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869773 | TATTTGACTTATAAA[C/T]AAAAACATAAAGGCA | 5521 |
rs374057317 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884002 | CTTTCTAGTTCTGCT[C/T]TGAGTGACATCATTA | 5521 |
rs374065409 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615192 | AAATGATGAGTTCAT[A/G]TCCTTTGTAGGGACA | 5521 |
rs374072624 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973412 | ATTTTCATTTTGAGC[C/T]ACTGTTGGCACATTG | 5521 |
rs374077246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810633 | AAAGTTCATGTATGC[C/T]CTTTCCTTCACCTTC | 5521 |
rs374078236 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933651 | TGACCTATCGTGACA[A/G]ACGGAAGTTCTTTTT | 5521 |
rs374084310 | snp | C/T | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918566 | AGGATAAAGTCCAAA[C/T]GTTTTAACATAGTTT | 5521 |
rs374089217 | snp | A/C/G | 0.00478244 | 0.0486902 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788932 | TTGCTCACTGTTGTA[A/C/G]CCCAGCACCTGGCAC | 5521 |
rs374089764 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078525 | AGGCGCGGTGGCTCA[A/C/T]GCCTGTAATCCCAGC | 5521 |
rs374094903 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624160 | ACTGCAAACTTACTG[C/G]GTTTTCAGGAGGATC | 5521 |
rs374114732 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989611 | CTCGATACAATAAAG[G/T]CCTTACATGACAAAA | 5521 |
rs374115840 | snp | A/G | 0.000414659 | 0.014393 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691246 | ACAGTTTTATCTGTA[A/G]TGGGCAACCAGATTA | 5521 |
rs374123725 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970457 | AAAAATTAGCCATGC[G/T]TGGTGGCGGGCTTCT | 5521 |
rs374157876 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707982 | AATTTTTAACTTGTA[A/C]ACAATTTTAATTTGT | 5521 |
rs374166819 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698155 | TTACTCTGTAGGAAA[C/G]GAAAAAAATACACAA | 5521 |
rs374168629 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658050 | GCCACACAGAGTATC[C/T]TTGAGAAGCTTAGAG | 5521 |
rs374187355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779308 | AAACGAGACTGTCCA[C/T]ATCTTGTTTCCAGAA | 5521 |
rs374188505 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697755 | CTGCAGATAATGGGT[A/C]TCACATAATTGGGTC | 5521 |
rs374191441 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014485 | AGACTTGGAACCAAC[A/C]CAAATGTCCAACAAT | 5521 |
rs374202985 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802969 | TCAACATTAATAAAA[C/T]GTTCAAGGAGCTGGA | 5521 |
rs374203754 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816494 | TAATAGAGTTTATGC[A/G]CCTATTAAACATTAT | 5521 |
rs374208999 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770733 | GGTGTCGTCTGAGTT[G/T]GGACTTGAGAATGCA | 5521 |
rs374211866 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721941 | ATAGATGTAGAGATA[C/T]GCATACCCACACAGC | 5521 |
rs374214183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741232 | TTGTCTAGCAGGCAA[C/T]CCCCCTTTCTCCATG | 5521 |
rs374226903 | snp | A/G | | | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:147035205 | TCTCAGGAAACTTAC[A/G]ATCATGGCAGAAGGC | 5521 |
rs374228118 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634763 | TAAATCTCTTAACTT[-/AC]ACACACACACACACA | 5521 |
rs374251534 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597647 | TACAGGTTAATTTCC[C/T]TTTAAAGCAATTATA | 5521 |
rs374253101 | snp | C/G | 1.65151e-05 | 0.00287355 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592943 | AGACAATCTTTGGAA[C/G]GTTCTTCAGCCACAG | 5521 |
rs374264020 | in-del | -/AAGAG | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795629 | TACTTGAAATTTGCT[-/AAGAG]TAGATGTTATTCTCA | 5521 |
rs374267579 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073482 | AAGTGAAGTTGCATA[A/G]GAAATCCCCCTGTAG | 5521 |
rs374273036 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927764 | TTTTAGATGGAGTCT[C/T]ACTCTGTCACCCAGG | 5521 |
rs374309195 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820271 | CTCATTTGATTATTA[C/T]ACATTGTATACATGT | 5521 |
rs374319097 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665739 | TAAGCTTAATCATTT[A/C]TAGCTTTTGATTTAA | 5521 |
rs374321878 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146622360 | GTGCCATTATTGTCC[C/G]CATTTTATAGAGGTG | 5521 |
rs374343091 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648539 | CTGTATGTCAGAGTG[C/T]TCCACGTACTGGAAT | 5521 |
rs374350257 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830077 | GTATACAGTCAATGC[C/T]CAATAGATGTTTCTT | 5521 |
rs374353105 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632995 | GTCCATTACACCTGG[A/C]CAGTTTCTTCACCCA | 5521 |
rs374354263 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974847 | GTGCCCCCCACCACA[C/T]CTGGCTAATTTTTTT | 5521 |
rs374355923 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955773 | AGTCTTCTTTCTATT[-/AC]TTTTTTTTTTTTTTT | 5521 |
rs374360164 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660694 | ATGTCCCTAATTTCT[C/T]CTTTTACTGGCTTTG | 5521 |
rs374362403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616758 | AAAAGGGAACACTTG[C/T]ACATTGTTGGTGGGA | 5521 |
rs374365018 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863869 | CACACCGACTCCCAA[A/C]TGTAACCCCCAAAGA | 5521 |
rs374365804 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871056 | AATCTGTGCTTTCTG[C/T]GAGATAGTTATGTTG | 5521 |
rs374367607 | in-del | -/CACC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077309 | ACACACACACACACA[-/CACC]CACACCCACACCCCT | 5521 |
rs374371606 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888087 | GTGTACACTCCTCAG[A/G]CTCACTTGGTAGCTC | 5521 |
rs374377794 | snp | C/T | | | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878090 | CAGCAGGCTTACTTG[C/T]GTGGGAACCAGAAGC | 5521 |
rs374397522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634024 | TGTGGTTAATGTTAT[A/G]TATTAGCTTGACTGA | 5521 |
rs374406133 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682161 | AGCATAACAAAGGTA[A/C]CTTTGGGATGAAAGA | 5521 |
rs374416018 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078462 | CCAAAGCCAGTCCAC[A/C]ACATCAGAATTAACT | 5521 |
rs374425121 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618529 | AAACTATCCTCCTCC[A/G]TTTGTCAACAAAGGG | 5521 |
rs374444823 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677766 | CTCCTGAGCTCAAGC[A/G]ATCCACCCACCCCAG | 5521 |
rs374450097 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063312 | GCCTTCTGGTAAGAG[A/G]TTAACAGTAACAGTT | 5521 |
rs374454851 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047418 | ACCCCATGAATATGT[A/G]TAATTATTTGTCAAT | 5521 |
rs374464203 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863291 | ATTAGTCATTGCAGG[A/G]TATGTCAGCTGGAAA | 5521 |
rs374467389 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994894 | GGGAAAGACCAAAAA[C/G]TATATAGGCAATTAC | 5521 |
rs374476952 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656175 | GAGTTGGGTAAGGGG[-/G]CTAGCAAGCGAGAGG | 5521 |
rs374480686 | in-del | -/GCTAGGTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949116 | TACATGTGCTAGGTA[-/GCTAGGTA]CTTACAGATGATTAG | 5521 |
rs374481252 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915388 | TGCCCAGCTCTCTCT[C/T]ATTCATACATCATCT | 5521 |
rs374491707 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047250 | ACCACTGTATGATGA[C/G]TATAGTTAACAATAA | 5521 |
rs374492132 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777486 | GAGAAATGAGAAGTT[A/G]TCACTTAATGGGTGC | 5521 |
rs374503949 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796627 | CTGGCTCATAATTGA[C/T]GATTAATAAGGATTT | 5521 |
rs374506009 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772991 | GTCAAATAGCACTCA[A/G]TAAACATCACAAATG | 5521 |
rs374506606 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746384 | TTGGACTGGGAGTTT[A/T]AAAAAAAAAAGTCAT | 5521 |
rs374509627 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607332 | GGGGCCTAATGACAT[A/T]GTCTCCAGACACAGA | 5521 |
rs374510326 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731518 | TCCCTCTTCATTTTC[C/T]GTGGCTTCCCGTAGA | 5521 |
rs374516641 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885187 | ATTTTATTCTAACAA[-/C]CAGCCTCTATACAGT | 5521 |
rs374522170 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062498 | AACCTAAAATACATA[-/T]CATTATTTTATCTGT | 5521 |
rs374546572 | in-del | -/AA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771327 | CTGGAGACAGATGAT[-/AA]AGTCTCAGCTTCTGA | 5521 |
rs374556240 | in-del | -/ATTTTTTGTTG | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589528 | GAGTAAACGGTGTTT[-/ATTTTTTGTTG]ATTTTTTTCAATCAA | 5521 |
rs374557094 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934077 | TTCTTAATCAAGTCT[A/G]TCATTCTTGGACATT | 5521 |
rs374558581 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946890 | GGGGTAGGGGTGGGG[-/G]TATCCGTTTAGACAG | 5521 |
rs374572157 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655594 | AGCTGAGGCAGAAAG[C/G]TGAAGTTGTCTGAAG | 5521 |
rs374574203 | snp | C/T | 0.000165986 | 0.00910854 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:146856575 | CTGTCTTGGGTTCTC[C/T]CTTGGCTCCTGTGAC | 5521 |
rs374579350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649185 | GGCAGGGCTCATGGA[C/T]AGATGGAGTTAGAGT | 5521 |
rs374584034 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060605 | AGCACTCCAGCCTTG[G/T]TGACAAAGTAAGTGA | 5521 |
rs374584586 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675881 | TAATGATTTATATGT[C/G]GTAAGCAGTTCTGAC | 5521 |
rs374591861 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625870 | AAGGTCCTTAAAAGT[A/G]GAAGAGAGAGGCAGG | 5521 |
rs374598987 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767821 | CAAATGTAGCATGAC[A/T]CGTATCTACCACTAT | 5521 |
rs374601604 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010632 | GAGCTCAGGCAGTAA[C/T]GCAAGTGATGGGGTA | 5521 |
rs374603939 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677466 | TTCAGGATTGCTTTA[C/T]TTTTCACATTAATGG | 5521 |
rs374604408 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704680 | TCCACAAGATGGTGG[C/T]CTGGTAACCCCATTT | 5521 |
rs374605090 | in-del | -/TT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768901 | TACTTTTTTTTTTTT[-/TT]GAGACAGTCTCTCAC | 5521 |
rs374609631 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790960 | GGACAAAAGTCACAA[C/T]GAATGCTGCAAATCG | 5521 |
rs374613299 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618457 | GTTAATCAATTTGTG[A/T]TATTTTAAGCCACTA | 5521 |
rs374625813 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844379 | AACATTAAAAAAAAA[-/A]TATATACTGAAACAT | 5521 |
rs374635216 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904344 | ATAAGAACATTATTA[C/T]AAAAGGAGACCAAAG | 5521 |
rs374638679 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777316 | TGAAGTTCTAATACA[C/T]GGTAAACATGGATGA | 5521 |
rs374670560 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027406 | TTGTGAGGCAGAGGC[C/T]GGCGGATCATGAGGT | 5521 |
rs374671270 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960908 | TTTATAAAACCAATG[C/T]ATGCCTATTGTAAAA | 5521 |
rs374683424 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910353 | ATAGGTTACTTAACT[C/T]AGATTTGAGACAAGG | 5521 |
rs374725300 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713326 | AGGAGAAATGGGAGG[G/T]TCACATGATATAGAG | 5521 |
rs374728319 | snp | C/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838148 | ACAGCTTGGTAGACC[C/G/T]TGTGTTGGTATTTGC | 5521 |
rs374734220 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682279 | CTAGTCTCTAGATGT[A/G]ATACTACTTCGAACT | 5521 |
rs374743637 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719360 | GTAACATAATGAATG[C/G]TTAACAGAATGACTT | 5521 |
rs374753032 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945793 | TGTGTAAGGCAATTC[A/G]ATTTGAGAAAGAATG | 5521 |
rs374753881 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744468 | TCCAGTGACAACACA[C/T]AGGCTGGGACTGAAG | 5521 |
rs374754667 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809650 | AGGAGTGGGCCACGA[A/G]GCTGTGGGCACACAG | 5521 |
rs374763186 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735668 | GGAATGGCTATGGAG[C/T]GGCCTGAGGGTAGAG | 5521 |
rs374767246 | in-del | -/CACACACA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740574 | ATTTTAAAATGAGAT[-/CACACACA]CACACACACACACAC | 5521 |
rs374783257 | snp | C/T | 1.64931e-05 | 0.00287163 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146691207 | TCTGGCCTCTTATCA[C/T]GCTCGCTGACTTTCC | 5521 |
rs374790682 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749606 | TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 5521 |
rs374798202 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788722 | TGGGTGACAGAGAAA[A/G]GCTCTATCTCAACAA | 5521 |
rs374800691 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788686 | CAGTGGTCCGAGATC[A/G]TGCATCATTGCATTT | 5521 |
rs374801929 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764845 | ACACGCACACACACA[C/T]GCACACGCACACGTA | 5521 |
rs374807189 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810057 | TTGAGAAGCTGGTGG[A/G]TAGTGGTGCTGTGTG | 5521 |
rs374809336 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811096 | GCAACCTCCGCCTCC[C/T]GGGTTCAAGTAATTC | 5521 |
rs374813302 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666576 | CTGTTCCCAGAGTGG[-/A]ACAGGGAGTCAGCCC | 5521 |
rs374817486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885100 | ATTGATTCATTTATA[C/T]AGTAATTATAGCTAA | 5521 |
rs374842222 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715903 | TGTATCTTCTGGGCT[C/T]AGTCTTCACTTTTCC | 5521 |
rs374843523 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924464 | ATGGGCCCTTCCCAA[A/G]TACTGGAGATTTTAA | 5521 |
rs374845357 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851143 | TCATGCAGTAAAGGT[C/T]CACAATGGTGCCAAT | 5521 |
rs374846446 | snp | A/T | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864159 | AATTATTACAGCAAT[A/T]TTGGAAAGAATCTAA | 5521 |
rs374851508 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744588 | CAGGGAACCATCCTG[C/T]GTGCTCCATCAGCAC | 5521 |
rs374855516 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985255 | CGAACTCCTGATCTC[A/G]TGATCCACCTGCCTC | 5521 |
rs374856932 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873240 | ATCTTTCTCTATTAC[A/G]TATCTTAAATCCATC | 5521 |
rs374875883 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078908 | TTAAAAAGTTCAAAT[G/T]ATTTTGAATCATGGC | 5521 |
rs374876136 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648065 | GCTGTGTACCAAAAC[C/T]GGGTCTTTTTATCCT | 5521 |
rs374891539 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620487 | GGCAGTGAGCATCTC[C/G]ACAGGAGCCTAATGA | 5521 |
rs374902098 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772408 | TATATATATATATAT[A/T]TATATATATATATAT | 5521 |
rs374910666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731629 | TGCAAAACCTTGGGA[C/G]AGTCAGTCACCCTCA | 5521 |
rs374925523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658322 | GGAAATTCCAGATTC[C/T]GGCCTCGCTTCAAAT | 5521 |
rs374926065 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740046 | CAGATTCTCAAAGGA[A/G]CCTAAGACCTCACAA | 5521 |
rs374930484 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793046 | CAAAGTATGTTAGAT[A/T]CTTGCTTGCATCAGC | 5521 |
rs374944996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920675 | GGAAGAGGCTGGCTA[C/T]GGGGGAGAGAGCCCC | 5521 |
rs374949646 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841353 | AGAGTTTTTAAAGAC[G/T]CTGTTCAGTCCAACT | 5521 |
rs374959691 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692622 | CACTGCAAGCTCTGC[C/G]TCCTGGGTTCATGAC | 5521 |
rs374971864 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788178 | GTGTCTTCTACTGAG[C/T]CTAGCTATATTTTGT | 5521 |
rs374973034 | snp | A/G/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768417 | AAGAAATTCCTGGGG[A/G/T]TGAAATGGTTAACAG | 5521 |
rs374987312 | in-del | -/GGTTCTCTCT | 0.0150606 | 0.0854603 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922889 | AACTACGAGGGAAGA[-/GGTTCTCTCT]CCCTGTTGGAGATTC | 5521 |
rs374991952 | in-del | G/TTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734061 | AATGAGTTAGGTTTT[G/TTT]TTTTTTTTTGAGACA | 5521 |
rs375031966 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070484 | AATTCCATTAACTAA[C/T]AGCATAGGCAGTAAG | 5521 |
rs375033414 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009864 | ATATACACACACACA[C/T]ACACACACACACACA | 5521 |
rs375039304 | in-del | -/TGTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708408 | GTATGTGTGTGTGTA[-/TGTG]TGTGTGTGTGTGTGT | 5521 |
rs375040424 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834171 | ATAGTAACATGTATT[A/G]AGGGCATACACCATA | 5521 |
rs375041990 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020576 | ACCAGGAGGGGTGGA[A/G]AAAGAAAACAAAAAG | 5521 |
rs375042856 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745616 | CACATAAACTGCTTG[C/T]CTTCTGGCATGAAGA | 5521 |
rs375069465 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984622 | GATTGCTGAATCATA[C/T]GGTAGTTCTGTTTTT | 5521 |
rs375077990 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594637 | GCATGAAGCACAGAG[A/T]TATGACATCATTTGT | 5521 |
rs375080630 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945139 | TAACTCCTGATGAAT[A/G]CCTGCTTTGTACTTC | 5521 |
rs375092323 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892561 | TTAAGATCATCAGGC[C/T]TTCAGTCTTTACCCC | 5521 |
rs375099200 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696173 | CGGTGGAGTGATCTC[A/G]GCTTACTCCAAGCCC | 5521 |
rs375099914 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957734 | GTTGCAATAACGTTC[C/T]GACCTATGGTAACAC | 5521 |
rs375127619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043251 | GACTAAATTGTGTCC[C/T]CCTGCAAAGTCATAG | 5521 |
rs375135713 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618694 | CTTCTGGGCAGAGGC[-/C]ATGAGAGGCTCACTG | 5521 |
rs375173241 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738517 | GCAAGATTTCACCTG[A/G]GGAACTCTTGTATTC | 5521 |
rs375181971 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741201 | AAGGATGGAGCACAT[A/G]CAGTAAGGAAGGTTC | 5521 |
rs375189132 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790006 | AATGCAGAGGTAAAA[C/T]GTAATCACAACACAA | 5521 |
rs375196434 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596101 | CTCTGCCATTGTGCA[C/T]GGAAGCAGCCATAGA | 5521 |
rs375199206 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767396 | AAGACTGTCACTGAC[C/T]CTGCAGCTGGTTCTT | 5521 |
rs375218587 | snp | G/T | 0.277867 | 0.248442 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615473 | TAACCTGCACAATGT[G/T]CACATGTACCCTAAA | 5521 |
rs375223499 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919911 | AATTAAACCAGTTTG[C/T]GTATCATGGCAGCCA | 5521 |
rs375234124 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845502 | TCGTGATCCGCCCGC[C/T]TCGGCCTCCTAAAGT | 5521 |
rs375243659 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901614 | TTCATTATACCTGAG[-/G]TCCTAGATGCTGTGT | 5521 |
rs375244736 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042601 | TTATTCATTCATCCA[A/G]CAAAGATTTATCATT | 5521 |
rs375255425 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147076682 | CCTCTTTGGTAGTCT[A/G]AGCATTGTAGTCTTT | 5521 |
rs375255567 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983282 | ACCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 5521 |
rs375260338 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680084 | CATGCTGCTATAAAG[A/C]CACATGCACACTTAT | 5521 |
rs375263844 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961217 | CATAAACACTTAAAT[A/T]GTCCCGATAACAGCA | 5521 |
rs375269322 | snp | A/G | 1.68261e-05 | 0.00290048 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691081 | CATGGCCAACCTTAG[A/G]AGACCTGCCCCTGAC | 5521 |
rs375273794 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725405 | CTGGAAAAAAAATCC[A/G]TTTCAGAAAAAAATA | 5521 |
rs375305542 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958069 | ATCTATTTTTTTTTT[-/T]CTCCAAATGTTGCTG | 5521 |
rs375315736 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846314 | AACCTGGGAGGCAGA[C/G]GTTGCAGTGAGCCAA | 5521 |
rs375318020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943968 | CAGCCTCATTGACAT[A/G]TGTTCAAGGAGAGGC | 5521 |
rs375324860 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146878979 | TTCCAACCTCCTCCC[C/T]TCTCGCGCCACTCAG | 5521 |
rs375331591 | snp | C/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859429 | AGGGGCAATTCTTAA[C/G]AGTTGAAAACTATCA | 5521 |
rs375346207 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590914 | AAAAGATTTTATATG[G/T]TTTTTTTCCCACACT | 5521 |
rs375346612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004395 | TGCTGAGCCCTGGGT[A/G]CATTTAACCATTGAG | 5521 |
rs375355073 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958154 | CAGACATTAATCGCA[A/G]ATCTCCCGAAGGCCC | 5521 |
rs375360620 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888430 | CACCATCTCCACTGC[A/T]GCTACCATGCTCCAA | 5521 |
rs375364229 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935657 | GTGTGAGCCAGGTAA[A/C]GGAGGATTGAAAGTA | 5521 |
rs375366202 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985981 | GATGGCATAATAGAA[C/G]CCTCTGACAAGTATC | 5521 |
rs375372230 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659939 | GCATCTCTTCCATCC[A/T]CCAAGGGAATTCAGT | 5521 |
rs375376283 | snp | C/T | 0.000362905 | 0.0134655 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600314 | TCTCGATGGGGCGGT[C/T]TTCCATGTTGAGATC | 5521 |
rs375382153 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662596 | AGCCTCTAATACTGT[G/T]AGAAATAAATTTCTT | 5521 |
rs375387248 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615805 | ATCAATACTGCTAAA[A/C]TGTCCATGCCACCCA | 5521 |
rs375397198 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690879 | TAAGATTATAGTAAC[A/G]TCTGGCAGTGGCCAT | 5521 |
rs375409964 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048426 | TTATCTCATAATATT[G/T]TTGAGAGATAGTAAC | 5521 |
rs375412148 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692564 | TTTGAGACAGAGTCT[C/T]GCATTTTCACCCAGG | 5521 |
rs375413576 | snp | A/G | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081974 | AGTCCTTTACAGAAC[A/G]CTTCTGGATAGCAGG | 5521 |
rs375413594 | snp | A/G/T | 0.000115628 | 0.00760275 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600303 | TACCTGGTAAGTCTC[A/G/T]ATGGGGCGGTTTTCC | 5521 |
rs375420586 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680141 | CAAAGACTTGGAACC[A/G]ACCCAAATGTCCAAC | 5521 |
rs375433881 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005063 | AGATACCAGGCACTA[C/G]TCCTTGAGGGACCAG | 5521 |
rs375437529 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027634 | AGCGAGACTCGGTCT[A/C]AAAAAAAAAAAAAAA | 5521 |
rs375442716 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678295 | AAAGACAAAAACCAC[A/G]TGCTTATCTCAATAG | 5521 |
rs375464821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034310 | ACTATCCTGTATTAT[C/T]TTCTTCACATTTTTT | 5521 |
rs375464942 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759690 | ATACACACCCTATTC[G/T]TCATAATAACATATA | 5521 |
rs375470692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785549 | TGAGACCCTGTCTCA[A/G]AAACAAACAAACAAA | 5521 |
rs375471972 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742777 | TGAGGTCATTAGGGT[A/G]GGTCCTAATTCAATA | 5521 |
rs375480397 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681992 | GTGTACATATGGGAG[C/G]TGTCCTTTATTAGTT | 5521 |
rs375493152 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915799 | CAAATTCTTGTGCTT[G/T]CCTCCTCCTTGCTAA | 5521 |
rs375496890 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881907 | TCTAGCTCATAAGCT[A/G]TATTCCTATTGAAAT | 5521 |
rs375513011 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866609 | TAAATTATATATATA[A/T]ACACACACGCAGATA | 5521 |
rs375524945 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899359 | AATCATCATTCTCAG[C/T]AAACTATCGCAAGAA | 5521 |
rs375550400 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952132 | ACTGAAAATATTATT[A/T]TCATGATCTTCAATA | 5521 |
rs375600448 | in-del | -/C | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861054 | CAAACTGAATTTTTT[-/C]TTTTTTTTTTTTTTT | 5521 |
rs375619064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784300 | GACAGCCTCAGTCCT[C/T]TAAATGACTGGATTG | 5521 |
rs375630041 | in-del | -/CTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716813 | CTTAGCTGGCATCTT[-/CTT]ATCAGGCATGACTCA | 5521 |
rs375632133 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590112 | ACACACTTTTCGGGG[C/T]TTGAGGATAGCCCGG | 5521 |
rs375637232 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047132 | GGGTTCTTCCTATCA[A/C]CATGTTGTATCAAAA | 5521 |
rs375644893 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650372 | GTAATAACAATATTT[A/C/T]CCTAACTTTATTGTT | 5521 |
rs375651126 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607718 | ACAGACCAAAAATTC[A/C]TAGTGGGGAGAAGTG | 5521 |
rs375653647 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854888 | TCTTAAAATTTGGAC[C/T]CTGAACTGTCTCTCG | 5521 |
rs375660001 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590742 | AGATGCTAGTGGCAT[C/T]GTGCACGAACCCGGG | 5521 |
rs375668454 | in-del | -/AC | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667926 | CAAGCAGGCAGAGAA[-/AC]AAAGTGGGAAGAAGG | 5521 |
rs375669409 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997856 | AATTAAGGCAAATAT[A/G]AGTGCTGGGTTTTGA | 5521 |
rs375673392 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960011 | ACGGAAATGTCATGA[A/T]CACTTTTAGTTGATT | 5521 |
rs375681330 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029250 | TCAATATTTTATCTT[A/G]TGTTATAGTCTAGAA | 5521 |
rs375682722 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943016 | GTTAGCCAGGATGGT[C/T]TCGATCTCCTGAACT | 5521 |
rs375686203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630108 | GCATAAGCCACCATG[A/C]CTGGCTGTGGCCTCA | 5521 |
rs375686569 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939639 | AGGTGAACTGGACCT[C/T]CTGCTTCATAGAGGA | 5521 |
rs375687507 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991559 | TGTATATTTCAAGAT[A/G]GCTAGAAAAGAAGAT | 5521 |
rs375691819 | snp | A/T | | | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923178 | ACTTGACACTAAAAG[A/T]TTCTCAATATATCTA | 5521 |
rs375699828 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595388 | CCTTTCCTCATCTGT[A/C]ACCATTCACCTTCGG | 5521 |
rs375700989 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924750 | TATGTAGGCCATCCT[A/G]CTTGTTATAGATTTT | 5521 |
rs375712572 | snp | C/T | 0.000467977 | 0.0152895 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856492 | GTATAAATAATAATA[C/T]GAATACCTTTATTTC | 5521 |
rs375714083 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667397 | AAAAGTAAACAGGAT[A/G]GGATGAGCAAGAGAA | 5521 |
rs375721276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063523 | CAATTATTCAGTGTA[C/T]ATAATGCCTCAAAGC | 5521 |
rs375726994 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015781 | AAAATAATGTAATAT[A/G]CATTCTTAATATAAG | 5521 |
rs375749867 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680935 | AACCACCCTTGTAAG[C/T]AGTTTTCTCCAACCA | 5521 |
rs375757934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146738161 | CAGCACTTTGGGAGG[C/T]TGAGGCGGGCGGATC | 5521 |
rs375763164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647331 | TCTCCTTTGTGAATA[A/C]GGGGCATTGTGGAAA | 5521 |
rs375778565 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726177 | CCATCCTCTAAAGCC[A/T]CCTTCTCCACCACTG | 5521 |
rs375790267 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977001 | CCATTTCATATAATA[A/G]CAACTTCATCTTTCT | 5521 |
rs375791606 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649716 | AGGCCTCCCAAAGTG[C/T]TGGGATTATAAGCAT | 5521 |
rs375795131 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652073 | TACTAGGAAAGGAAA[A/G]GGAAGGAAAGTCTTT | 5521 |
rs375814541 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734170 | AGCAGATCCTCCCAC[A/C]TTCGCCTCCCAAGTA | 5521 |
rs375832922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074680 | CGAATTTCTTAAACA[C/T]CCATGCAAAAGGAAA | 5521 |
rs375835339 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772406 | TATATATATATATAT[A/T]TATATATATATATAT | 5521 |
rs375839852 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615307 | AATTGAACAATGAGA[A/T]CACATGGACACAGGA | 5521 |
rs375864986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907736 | CCATACCACTTTCAT[C/T]TTCTACTGCTTTGAA | 5521 |
rs375870483 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004959 | CAGAGGCTATACAAG[A/G]AAAGGATCTTACTGT | 5521 |
rs375877731 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014644 | CGCAAGAACAAAAAA[C/T]CAAACACCGCATATT | 5521 |
rs375877869 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034204 | GAAGATCCTCTCCCC[C/T]GGTTTTTGTATGGCT | 5521 |
rs375880724 | in-del | -/A | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591673 | AAGAGATTATTTTCC[-/A]AAAAAAAAAAAAAAA | 5521 |
rs375889454 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770431 | TAAAAAGAATCCTTA[A/G]TGATGTGAAATTGTT | 5521 |
rs375891325 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877630 | TTCGCTCAGGGAGGG[A/G]GGACCAAGGTCCTAC | 5521 |
rs375892368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608099 | AGACTTGGCTGTATG[C/T]CATAGTTTGCTGAGC | 5521 |
rs375896465 | snp | A/T | | | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918841 | GTTTTCCCTGTTGTT[A/T]GCTTCCAAGGTTAAA | 5521 |
rs375897009 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788351 | TAAAGAAAAAAAAAA[-/A]GGGAACAGTAACCTC | 5521 |
rs375901201 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602091 | GCATATACCTCATCT[A/G]CTACATATTATTTCA | 5521 |
rs375901411 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950332 | AAGAAGTACTGTTAG[C/G]TTTTTAAAGCACCAT | 5521 |
rs375908094 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814860 | GATCTCTCAAGTTGT[A/C]TGCTTGGCCCTCTTC | 5521 |
rs375912197 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014213 | ACCAGTTAGAATGGC[A/G]ATCATTAGAAAGTCA | 5521 |
rs375914130 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847107 | CCATCATCTAGGCCA[C/T]CGTAATCTCTCAACT | 5521 |
rs375935676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620851 | TGGGGAGCCTCTGCC[C/T]AGGTGGAAGAGCTCT | 5521 |
rs375935786 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710093 | TGTTTTTCCTCCTTC[C/T]CCTGCTGTGGAGATG | 5521 |
rs375936116 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904329 | ATGCAAGTTTATTAT[A/G]TAAGAACATTATTAT | 5521 |
rs375938496 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011307 | ATAAATGCCCCCCCC[-/C]ATCCCTACATAGGAG | 5521 |
rs375957359 | in-del | -/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146591672 | GTAAGAGATTATTTT[-/C]CAAAAAAAAAAAAAA | 5521 |
rs375962149 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879114 | CAGGAAGTCTACATC[A/C]AGGTCCCTTTTCCTC | 5521 |
rs375963529 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001951 | TTCAGGGTCCTGACA[A/G]CAAGTTGGTTGACCC | 5521 |
rs375964369 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834693 | AGGTTTGTTACATGA[C/G]TAAATTGTGTGTGTT | 5521 |
rs375977295 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060650 | AAAAAGAAACAACAA[A/C]AAAACAAAACAAAAC | 5521 |
rs375983388 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032705 | TCTTATTTATGGCTG[G/T]GTAGTATTCCATCTT | 5521 |
rs375992134 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639082 | ACGGATGCTCCATGT[A/G]CATAAAGAAACTTGC | 5521 |
rs375994796 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031412 | TCATAGTAGTATGTG[C/T]TTCTCTCTATTTTTA | 5521 |
rs375995086 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052141 | TGTATCTTCTTATTT[C/T]AAGTTAAAGAACATT | 5521 |
rs376014475 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065130 | TTCATGCAGAGTATG[A/G]ACTAGTAGAGAAAAC | 5521 |
rs376016221 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999001 | CCTGGGAGACAGAGC[A/G]AGACTCCATATCAAA | 5521 |
rs376016395 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980374 | GGATAAATGCTTCAG[A/C]TTCTTTTTAATACTT | 5521 |
rs376016421 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974175 | TGCATATTTTAAAAG[A/C]ACAAAAAAGTCAAAA | 5521 |
rs376021035 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043511 | TCTGATACTTTCAGC[C/T]TCCAGAACTGTGAGA | 5521 |
rs376022103 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001647 | GGTGACCATGAAGGG[A/G]CCATCGCCTATCGCC | 5521 |
rs376033076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933923 | ACCTATGAGTGAGAA[C/T]ATGCGGTGTTTGGTT | 5521 |
rs376033425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935291 | ATGTGAGGTACAGCT[A/G]GAAGGCACTGTCTAT | 5521 |
rs376041991 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972107 | CTCCGTCTTCCTTTG[C/T]TCTTCATGACCTTAA | 5521 |
rs376045938 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657526 | TAATCAATTATGTTA[C/T]GGAAGGAGCATCCAC | 5521 |
rs376057252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931967 | TTCCCCCAACCTCCA[A/G]CAGCATATCCATGTC | 5521 |
rs376062538 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888428 | CTCACCATCTCCACT[A/G]CTGCTACCATGCTCC | 5521 |
rs376064403 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002080 | GTCAAACTTCCTCTT[G/T]CCTCTCTTCTCCGAG | 5521 |
rs376069763 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606976 | TTCTACAGGGAAGCA[C/T]GGCTGGCACGTTCTT | 5521 |
rs376080229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681396 | TGTACATGCCTGCAC[A/G]CACCCACACATGCAC | 5521 |
rs376088298 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919940 | CACTGATATAGCTCT[G/T]CCTCTTAATAGTTGT | 5521 |
rs376093414 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944610 | GATTTAAAGAGAAAA[A/G]AAAAGGAAGAATACT | 5521 |
rs376097539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637399 | AAACATCCTACAATG[C/T]ATAGGACAGCCCCTT | 5521 |
rs376099885 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875023 | GCTGATGGTTAAAGG[A/T]AAATGAAGTAGTGCA | 5521 |
rs376104422 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625225 | ATTTTGTGCTTTTTT[A/G]TTGCCATTTTCCCAC | 5521 |
rs376119656 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929181 | TCTCACTCATTCCCA[C/T]ATTTCTGTTCTTTTC | 5521 |
rs376121437 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958272 | TTATCTGGGTCCTTG[A/G]AGCCCTTTACTCTAT | 5521 |
rs376130895 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956424 | TCCCCAGAAAGCTTG[C/T]TCAAGATTTTATCCA | 5521 |
rs376131183 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936217 | CTTTTGAGAGTTTAG[A/C]CCTATCCTTTGTTTC | 5521 |
rs376139270 | in-del | CC/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652766 | GGAGGCAACACCCCC[CC/G]CCAAAAAGTTTTGCC | 5521 |
rs376166013 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863097 | CTTACCAAGTTTCTG[A/T]TCTCTGACCCCAGAA | 5521 |
rs376171654 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787360 | CAAGGGAAGATAGAC[A/G]CATAGATTTTTTTAA | 5521 |
rs376177971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077999 | AAAACAATGTTTAAA[A/G]AGCAGGGGCTTTGGA | 5521 |
rs376183139 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896093 | ACATTAAAGAAAGGC[G/T]ATGGTCAGGCTTTTG | 5521 |
rs376197977 | snp | A/G | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861540 | CTCAGGTGAATATTC[A/G]CTACATTAATTCCCA | 5521 |
rs376206427 | in-del | -/T | 0.0287284 | 0.116357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840333 | TTACCCCTTGGAATC[-/T]TTTTTTTTACATCGA | 5521 |
rs376231376 | snp | C/T | 1.6486e-05 | 0.00287102 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593080 | GGAGAGGAAACATAT[C/T]GAGAAGGTCAGTTAT | 5521 |
rs376238319 | snp | A/C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596307 | ATCTGTGAATGCATG[A/C/T]ATGAAAATGTATAAT | 5521 |
rs376247305 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922650 | CACATAGCATTCTCC[C/T]ACTATCCTGGTAACA | 5521 |
rs376269229 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030537 | TCCATTTACAATTAA[C/T]GTAACTACCATAGGT | 5521 |
rs376282867 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747910 | AGGACGATACGAAGG[A/G]TGATATGAACTGAGG | 5521 |
rs376288595 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801165 | ATAGCAGTTACCAGG[G/T]CCTGAGGGGGTGGGG | 5521 |
rs376302217 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958688 | ATAAATACTAGAGCC[A/C]GGATATAAACTCAAG | 5521 |
rs376304933 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941383 | AAACATGAAAATTAT[G/T]ACAAACCGGCCTGAA | 5521 |
rs376313502 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619366 | GTGCCTGTAATCCCA[C/G]CTCCTCCAGAGGCTG | 5521 |
rs376315854 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980663 | TCTCTCTTGTTTTTT[-/T]ATGTATTCTAATTTT | 5521 |
rs376319923 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859307 | CACAAGTATAAGATG[A/G]CATTACTATTTTACA | 5521 |
rs376324508 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906392 | CAATGGCGCGATCTC[A/G]GCTCACCGCAACCTC | 5521 |
rs376325451 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875514 | AAATTGAGTTTAGAG[A/T]CCTTCACACTAACTA | 5521 |
rs376328980 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869732 | TATCATGCTTGAATC[C/T]TTTTAAGTAAGAAAG | 5521 |
rs376331992 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058153 | ATAGTAAATATTAGG[G/T]GAGTAAGTGAATCGA | 5521 |
rs376339796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777923 | GGAGTAAAATTCCCA[G/T]CACTGAAGATACTAA | 5521 |
rs376343045 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843959 | ATAGTCCTTTGTGTA[C/T]ATACCCAGTAATGGG | 5521 |
rs376343248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948286 | GCTGCTTCCTAGGTG[C/T]TTGGCTTAAATATAT | 5521 |
rs376344483 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820393 | CATGCTAGGTAAAAT[A/G]GAGCAGCCAGTTAAA | 5521 |
rs376360359 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894008 | CCAAGATTGCGCTGC[C/T]ACACTCCAGCCTGGG | 5521 |
rs376363237 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624261 | TATCATTTTATGCCT[C/T]TTTAAAAACATAAAT | 5521 |
rs376369667 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831176 | TACTCCTTCTGCTTA[-/T]TAAAAAAAAAGTTAA | 5521 |
rs376378763 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730519 | CCCACCAAATCTCAA[A/C]CTGAATTGTATCTCC | 5521 |
rs376399557 | snp | A/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921001 | CTGCCTGGGCAGACC[A/T]AATTAGTCTTTTCTA | 5521 |
rs376405654 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615394 | CATTGGGAGATATAC[C/G]TAATGCTAGATGACA | 5521 |
rs376406654 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892573 | GGCCTTCAGTCTTTA[C/T]CCCTTCCAAGCCACG | 5521 |
rs376411613 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649513 | GCAGTGGTACGATCT[C/T]GGCTTACTGCAACCT | 5521 |
rs376412859 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069922 | CAGCCTCCTGAGTAG[C/T]TGGGATTACAGACGC | 5521 |
rs376425953 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707822 | CTACACATACCCACA[C/G]ACTCTCTCTCTATAG | 5521 |
rs376428334 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941934 | GTAGAGGAGAACCTT[C/T]TATTGCTTCTTCCAG | 5521 |
rs376430134 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912606 | ACAACCTGGGTTCAA[A/G]CAATTCTCCTGCCTT | 5521 |
rs376433805 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629345 | ACGAGTTATCTTAGA[C/T]TCTCCCTTTTCCATC | 5521 |
rs376434005 | snp | A/G | 1.82394e-05 | 0.00301983 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590252 | GAGAGCAAAGGCAAT[A/G]ACATATCTTCACTGT | 5521 |
rs376436233 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894632 | TTTAGTAGAAACGGG[A/G]TCTTCCCATGTTGCC | 5521 |
rs376451860 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892699 | GAGGCATTTGTTAAT[C/T]AGTGTTCTGGGAAAA | 5521 |
rs376456600 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671481 | TGCAGCTTTCAAACC[C/T]GGTAAAGGGTAGGAT | 5521 |
rs376461681 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758120 | CTTTGTGACAGGCCA[C/T]CCCTTCCTCTCAACA | 5521 |
rs376468496 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784841 | GTGAGTTCAGAATCA[C/G]ACATACTTGACTTGT | 5521 |
rs376475501 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823352 | ACAGGCGCCCACCAC[A/G]AGGCCCGCCTAATTT | 5521 |
rs376478611 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806761 | TCTCTGCCCTTTTTT[A/G]TCCTTGGCTGACAAA | 5521 |
rs376480491 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977799 | ATTTGGATTGGTTCT[A/G]AGTCTTTGATATTGT | 5521 |
rs376488773 | in-del | -/GTTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061974 | TTTGTTTGTTTGTTT[-/GTTT]TTTGGTTCTGAGCCA | 5521 |
rs376502531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742077 | TCAAACCTTCACGTT[C/T]TTACAAAGGAAAATG | 5521 |
rs376503804 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700043 | ATTACGATGCCCTTA[C/T]AGAAATTAATTGCAA | 5521 |
rs376516675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686819 | CTCACCACCCAACTT[C/T]CATTTCAGGCTGATT | 5521 |
rs376530960 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010234 | TTAGAGTCAGCTAGA[A/C]TAGTGATCCCCAACG | 5521 |
rs376545389 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055633 | GCCCACTTTTCCCAC[C/T]CACCCAGACACTCTC | 5521 |
rs376550781 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775268 | GGAAACCAAGCTCAA[A/C]AGCATATTGAAAGGA | 5521 |
rs376557943 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781912 | GTTGAATTGCAATCC[A/G]TAAAGTTGGAGGTGG | 5521 |
rs376563832 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760297 | TGAAGGAACTGAAGT[A/G]TATGGAATTTTTATA | 5521 |
rs376565974 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001175 | GTGGGTGGGGCCAAA[-/T]AAGGGAATAAAAGCT | 5521 |
rs376567992 | in-del | -/TGT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851896 | CATCTGTGGAGAAGT[-/TGT]AAATTTTTCAGATTG | 5521 |
rs376574437 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051600 | CGTGGCAAGTCACAG[A/T]ACCCTTGTCCCTTTA | 5521 |
rs376574662 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983401 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 5521 |
rs376582360 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911263 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 5521 |
rs376601564 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010325 | GAAGGGGGAATGGTT[C/T]GGGGATGGTTCAAGT | 5521 |
rs376603330 | snp | C/T | 1.69407e-05 | 0.00291034 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856453 | TTTAACACTTCTATA[C/T]TGCTACTTTATCAAG | 5521 |
rs376604470 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970184 | AGGCATAGAGAGAAC[A/T]ACTATTTCCTCAAGG | 5521 |
rs376605846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894086 | TCTGTCCATATCTAT[A/C]CATTTACGCTGCTAC | 5521 |
rs376613335 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628064 | ATTCTCCTGCCTCAG[A/C]CTCCTGAGTAGTGGG | 5521 |
rs376622051 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869415 | AACTACTAAATAAAC[C/T]GTGGTACTGTCATAC | 5521 |
rs376637973 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619467 | TCAAAAACAAACCCA[A/G]AATACAAACAAACAA | 5521 |
rs376639305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933459 | ATTCTCTCTCAGATA[A/C]GTATTTTGTCTATGA | 5521 |
rs376653746 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601177 | ACCACATTTTGTTTA[C/T]CCATTTTATGAGCAT | 5521 |
rs376658786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728769 | CACTTTTGCTTCTTC[A/G]TCATTTTCTCTTGCC | 5521 |
rs376660739 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596853 | CTACATATATGGCTG[G/T]GAATTCTGGCTCCCA | 5521 |
rs376661192 | snp | C/T | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082434 | AAATGGCAATAATAA[C/T]GGTACCCATCTCTCA | 5521 |
rs376677970 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993299 | CCAGGCTAGAGTGCA[C/G]TGACACCATGTTGGC | 5521 |
rs376686449 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901200 | TTATTGGTGCTAACA[A/T]AAAATATCTGTACAA | 5521 |
rs376690334 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014122 | TTTATGCAGCCAAAA[A/G]ACACATGAAAAAATG | 5521 |
rs376692735 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660977 | ACAAAGAGATGTATA[C/T]TGTTTCATGAGAGAA | 5521 |
rs376694693 | snp | C/G | 1.68872e-05 | 0.00290574 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600242 | GGGCTGACTTAAAAG[C/G]TCATGAAGGGAATGT | 5521 |
rs376696065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714680 | GTAAGAAAAATGCTA[C/T]TGAAATCTTCTCTTC | 5521 |
rs376696233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844979 | TCCAACTCCATTCCA[C/T]GGCTTACAAAGTCCA | 5521 |
rs376700738 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761688 | TTTTGTAGTCAGATT[G/T]CCTGAGCTGAAATTT | 5521 |
rs376705197 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879846 | TTCCTAGGTTTCATC[C/T]TGTAGAAGGTATTCA | 5521 |
rs376711584 | in-del | C/TACACACAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733710 | AAAACCACACACAGA[C/TACACACAG]ACACACACACACAAA | 5521 |
rs376721317 | in-del | -/GGCCTTGCCATTGA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016554 | CTGAGAAAACATAGG[-/GGCCTTGCCATTGA]GGACACAGTCACATA | 5521 |
rs376726440 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050926 | GAAGGAGCATTGTTG[A/G]TAGAATATGGGTCAG | 5521 |
rs376750307 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773686 | TTCCTGAGCAGCAGG[G/T]TTTGAGAATTCTCTT | 5521 |
rs376761624 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698711 | AGGTCTCACAGCTCA[G/T]AAGGAGCAGATTTGG | 5521 |
rs376766033 | in-del | -/CT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889642 | TTGCCTTATGCATCT[-/CT]TTCTTTGGTTTATTT | 5521 |
rs376773964 | snp | C/T | 4.94238e-05 | 0.00497086 | missense, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146701055 | CTTACCTCCTGCTCT[C/T]GTTGAAATATTACAA | 5521 |
rs376789704 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897409 | CTGGGGTGGACTAAG[G/T]TCACAAGTGTGGGAG | 5521 |
rs376791352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678089 | TTAAAAGCCATTGCT[A/G]TTGGGAGGCCAGGTA | 5521 |
rs376796617 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907219 | ATTACATTTTTTTTT[C/T]CATCAGCAGATGTAG | 5521 |
rs376797635 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931608 | CTCTAGTCGAGGGTA[A/G]ACAAGAGGCACTGGG | 5521 |
rs376801500 | snp | A/C | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916673 | CTCCAAACAGTAGCT[A/C]CAGATTCTTGCTATG | 5521 |
rs376802310 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595615 | CCTATCTGCCTCCAA[C/T]TGACAGCATTTAAAG | 5521 |
rs376804144 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680096 | AAGACACATGCACAC[G/T]TATGTTTATTGTGGC | 5521 |
rs376808896 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078596 | TTCGAGACCATCCTG[C/G]CTAACACGGTGAAAC | 5521 |
rs376814651 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604203 | GTGTTATCAGACGGA[-/C]AATCATGGTGCTATG | 5521 |
rs376816637 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030579 | ATTTTGGGCTAGGAA[C/T]GTATTTTTAACTTCT | 5521 |
rs376820292 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651817 | TTCAACCCAGGTGGC[G/T]AGGAGAAGAAAAACA | 5521 |
rs376825597 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807937 | CCCAAGTAGGTGAGA[C/T]TACATGTGCCTACCA | 5521 |
rs376829120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641630 | AGAGAAGTCTAGTTG[C/T]TAAAAATTAAGTGAC | 5521 |
rs376831970 | in-del | -/TGATTTCATCGATTTTCA | 0.0111196 | 0.0737302 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928213 | CACTTATTCCTTTGG[-/TGATTTCATCGATTTTCA]TGATTTTAAATCCCA | 5521 |
rs376835638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953987 | ATTTCTAAATTGGGA[C/T]ATGAATATCTACCAA | 5521 |
rs376837450 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865219 | CTGGGGCAAAAGCAA[A/G]CAAACAAACCCTATA | 5521 |
rs376840412 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908417 | TTACTTAAAAATTAA[A/T]TTTTTTTTTCTTTCA | 5521 |
rs376854426 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789230 | TGTGGGTGGAAAGGC[A/G]AGAGAAAATAGCCAA | 5521 |
rs376859058 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797771 | TTATCTGTATTTGTT[-/T]GTTTCAGAGCCTGAC | 5521 |
rs376881280 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953319 | CAATTTATAATATGT[C/T]TGAAATGTAATACTC | 5521 |
rs376881377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616511 | CAGAATATAGAAGGA[A/G]CTCAAACAATTCTAT | 5521 |
rs376883050 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823187 | TGCTCTGTGGCCAGA[A/G]TTTACTTCTTCTTCT | 5521 |
rs376884857 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887385 | AAATAAATTTTTACC[A/T]ACTAGAAACTTGAAT | 5521 |
rs376892407 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049480 | AAGTCTGCATTTTAG[A/G]TGAGAGATTGGAGTT | 5521 |
rs376896937 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669931 | TTATGGATTATCTAG[A/C]TCTTTAAACATGAAT | 5521 |
rs376897008 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818287 | CATAAGACAGCCAAA[C/T]GATATTTGTTGAATA | 5521 |
rs376898894 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852799 | AATGCAGGGAGCACA[C/T]TGGGAATTATCAGAA | 5521 |
rs376906022 | in-del | -/GAA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024904 | CTTCTACCACCATAA[-/GAA]TACGGAAAAAGAAGA | 5521 |
rs376909039 | in-del | -/AA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745207 | GAGAGAGAGAGAGAG[-/AA]AGAGACTATAAGCAT | 5521 |
rs376920736 | in-del | -/C | 0.00399041 | 0.0444891 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893011 | TTCACAAACCCTATG[-/C]CGCAGAAACAGTGGG | 5521 |
rs376923460 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632303 | GAGCAGTGTGGAACT[G/T]ATCCTTCTTTCGTAG | 5521 |
rs376924029 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623559 | ATTCTATTTTTCTCA[C/T]ATGTAACTCTTCAAT | 5521 |
rs376929696 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604107 | CAGCACTACTCCTAG[C/T]GAGCTCACAGGATAG | 5521 |
rs376937801 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077618 | TATTAATTCACTCAA[C/T]AAATACTCAACTTCC | 5521 |
rs376959573 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665441 | TTATTCTGCAGCTTC[C/T]TCCCCTCTGTCAGCC | 5521 |
rs376966770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660051 | GAATTTAAAAAGCTG[A/C]AAGCTCTCCTGGTTA | 5521 |
rs376979661 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018272 | AAATTGCAGAAGCAC[A/G]GATTTCCACTGGAAA | 5521 |
rs376980608 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727113 | CAGGGAATTCAAAAT[C/T]GCTCAGCTGTATGCT | 5521 |
rs376986593 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691679 | CATTGTCCTTACCAT[A/G]TCCTAAAAGGCCCTT | 5521 |
rs376987609 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147013576 | AGCCCTCAGAAATAA[C/T]GCCGCATATCTACAA | 5521 |
rs377002490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920845 | ACAGGTCTGAATCTC[A/G]TAGAATTCTGTTAGA | 5521 |
rs377005443 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898243 | AGATATGCAGCATTA[C/T]TTCTGAGGGCTCTGT | 5521 |
rs377011805 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797037 | AGTTTTGGGAGTTGA[C/T]CCTTTGTTAGCTCTC | 5521 |
rs377013149 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753180 | ATTTATCATGACACA[C/T]GTGGGTAAAAAGGGA | 5521 |
rs377028884 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693007 | CTCTGTCTTGCACAA[A/G]GTAGGGTTTGGAATC | 5521 |
rs377054519 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146761868 | GGCTTGATGAGGGAT[-/T]AAAAAAAGATGGGAC | 5521 |
rs377061539 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049197 | ATGGATGTGATAAGA[C/T]GCAATTGGATTCCTG | 5521 |
rs377071107 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776300 | GTACAGGGATAACAA[C/T]GGTTTTATATAACAA | 5521 |
rs377072298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980128 | AATGATATATTTTTA[A/T]GAAAAAAAGAAATTC | 5521 |
rs377074975 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609686 | CCTCACCTGGGAAGC[G/T]CAAGGGGTCAGGGAG | 5521 |
rs377077053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937028 | GTTACTAGGCTAGGT[A/G]TGGTTGCTCACGTCT | 5521 |
rs377083398 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940330 | TTCAAATGTGAACAT[C/T]TATTCCAAATCCAAC | 5521 |
rs377122785 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751785 | AGAGGGTGGGGGCAG[A/G]TCTTCTGGTGAACAT | 5521 |
rs377133436 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839028 | AACACTAGAAAATTC[A/G]TCCACATACTGATTT | 5521 |
rs377134477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823056 | TGGAGACACTCCCTC[C/T]ATGTGAACCAAAAGG | 5521 |
rs377139868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906961 | AGCCGAGTTACACTG[C/T]AGCAGGAGACAGGAT | 5521 |
rs377140312 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856750 | AGGTAACACAATCAA[C/T]ACTGTAAAAGCTTCC | 5521 |
rs377143229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925066 | CATTCCCTCTTCCCT[C/T]CTTTGTGCTATTACT | 5521 |
rs377143525 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873674 | TGGAGTGCGGTGTCG[C/T]GACCTCGGCTCACTG | 5521 |
rs377145150 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609367 | GAGCAATCAGACAAA[G/T]GAAGAAAAGGCATCC | 5521 |
rs377147944 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875198 | CAACATCCATTTAAC[A/T]GGGTTTAGATATATT | 5521 |
rs377160450 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684211 | AGCAGCAATAAATCA[C/G]AAAATGAAGTCTAAA | 5521 |
rs377162439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659192 | TAATGAGGTATTTAA[A/G]TCCCACTGGATGCAA | 5521 |
rs377176736 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656117 | AACAGTGAACTCTCT[G/T]TGGTACATAAGTTCT | 5521 |
rs377193928 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705986 | TTTGGACAGAAAAAC[A/G]AAACAAAACAAAACA | 5521 |
rs377210905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686548 | CATAGTAAGCACTCA[A/G]TAGATGGTTGCTATA | 5521 |
rs377214466 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828357 | GAAACTTCTGTATCA[A/G]TGACCAAATCAGTGG | 5521 |
rs377214473 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146961811 | TCCCCCATGGAGGAG[A/T]TTTTTTTTCAAAGGA | 5521 |
rs377216725 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914633 | ATTGCTGCAAAAAAA[C/T]GTTGTTGGCCAGGTT | 5521 |
rs377236116 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064906 | TTGGGCAGTAGAATG[A/G]ATTTTCTTGGAGTAT | 5521 |
rs377257403 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804505 | CTTTTAAATTGACTA[C/T]ATTTTCAATAACAAC | 5521 |
rs377259787 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045576 | TGACTGAGTGCTAAT[C/G]TGCTCTTAGCTCTTC | 5521 |
rs377263980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950834 | TTAGCACAAAATAGG[A/T]TACAAACAACATAGG | 5521 |
rs377269145 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620274 | GAATTTGGGCTAATA[G/T]GTACAGACAAGTTCA | 5521 |
rs377270841 | in-del | -/TTAAT | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928436 | CCATCTTGATTGATA[-/TTAAT]TTATCTGCTCAGATG | 5521 |
rs377287876 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859380 | CTGTTTGGAGAAGTT[A/G]GTTTATTGAAGAACT | 5521 |
rs377298404 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740616 | ACACACACACACACA[C/G]ACACACAGATAAAAG | 5521 |
rs377303073 | snp | G/T | | | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617395 | TAAAGAGTACATGCT[G/T]GAGGTGATGAATATA | 5521 |
rs377311611 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689169 | CTAACATCATTGAGT[A/G]CTTTTTGTGAGCCAG | 5521 |
rs377317665 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632974 | CCTTTCATTCCCCAG[A/G]TTGGTGTCCATTACA | 5521 |
rs377322934 | snp | C/G | | | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146765963 | TTGTTTTGGACAGAA[C/G]TTTTTAGACTCTCCA | 5521 |
rs377323975 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962413 | CCTGTAATCCTAGCA[C/T]TTTGGGAGACCAAGG | 5521 |
rs377333409 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990385 | TAGAAAAACAGACCA[A/G]TGGAACAAAATAGAA | 5521 |
rs377336472 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146910977 | TAGGCTGTTCCCAGT[A/C]TAAAATTCTTTTCCA | 5521 |
rs377338411 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807863 | GGAGTGCAATGGCAC[C/G]ATCTCAGCTCACTGC | 5521 |
rs377338471 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844220 | GGGTCGGGGGAGGGG[A/G]GCGGGATAGCATTGG | 5521 |
rs377355133 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927351 | TCATTTTCCCCTTTC[A/G]CACACTTAAGTCCAA | 5521 |
rs377376662 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899258 | GACTGGATTAAGAAA[A/G]TGTGGCACATATACA | 5521 |
rs377385157 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055018 | ATGCTAGGTTAGAAG[G/T]CAGCAGAGAAGGTCC | 5521 |
rs377389501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731529 | TTTCCGTGGCTTCCC[A/G]TAGAGTTTAACTGAC | 5521 |
rs377398508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972637 | GAATCACTTGAACAC[A/G]GGAGGCAGAGGTCGA | 5521 |
rs377399816 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589946 | GTAATAACTTGTCCA[C/T]CTAGTTAACCTTGTC | 5521 |
rs377400005 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847582 | GGGCTTGTGCTCTGT[C/T]GGTGGTGGATGTAGA | 5521 |
rs377400906 | in-del | -/CAATATTCCCTA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870020 | AGCAGCATCTTGCTA[-/CAATATTCCCTA]TTAGAGACATTTACA | 5521 |
rs377410804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838465 | AATCCCAGTTACTTC[A/G]GAGGCTGAGGCAGGA | 5521 |
rs377418958 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811273 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACGG | 5521 |
rs377441594 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870697 | CTCCGTCCAACAGAC[C/G]CCATCCTTCTCAGGT | 5521 |
rs377457061 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987970 | AGGGCAGGAGTAGCT[A/G]TACTTATATCAGATA | 5521 |
rs377462455 | snp | C/T | 6.65391e-05 | 0.00576759 | intron-variant, missense, synonymous-codon | PPP2R2B | GRCh38.p7 | 5:147055699 | AGAAAGGATGGTGTT[C/T]GGAGGTCTGAAGATG | 5521 |
rs377464332 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051743 | GACTCTCTCATTTCT[G/T]TTTTGCTTCCTTTTT | 5521 |
rs377464524 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844703 | GCAGCTCAACAAAGC[C/T]AGCTGGGTTTAGCAA | 5521 |
rs377467540 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829373 | GGTTATATGCTTAAG[C/G]ATAGAAATATTAATG | 5521 |
rs377469524 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927930 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 5521 |
rs377471418 | in-del | -/GTGA | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884406 | TGCCATGGTAGACTT[-/GTGA]GTAATTGCTTTTATA | 5521 |
rs377472573 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886669 | ATAAGCCAACTGCTA[A/C/T]AATTTTTTGGTTAAA | 5521 |
rs377479309 | snp | A/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771645 | GAACAATAAGAAAGT[A/T]TTAGCTGGGCACATG | 5521 |
rs377497129 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765120 | TCCAAATCAGTGAAG[A/T]TTTCTTATATGCTAT | 5521 |
rs377499836 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882218 | GGAGGCAGAGGTTGC[A/G]TCGCACCACTGCACT | 5521 |
rs377507819 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677211 | AAGATAATTGGACAG[A/G]GTTTTCGCTTTGTAT | 5521 |
rs377510314 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039126 | GGCTCTTCGCATTGC[G/T]GACCCTTTCCCATCA | 5521 |
rs377515377 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678573 | GAAGGAAATAAAGGG[C/T]ATTCAATTAGGAAAA | 5521 |
rs377518483 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033003 | TGTAGAAGTGTTCCC[C/T]GTTCACTGCATCCAC | 5521 |
rs377533872 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146796261 | CGTATGCTCCCATAC[G/T]TCCAAGTGTATACAT | 5521 |
rs377534220 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955476 | GAAAACTATAAATTA[C/T]GTCCCCAGATAAATT | 5521 |
rs377537216 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775455 | AATATCCTTTCATGA[A/T]AAAACCCTCAATACA | 5521 |
rs377569863 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694311 | CTGCATACCGAACTG[A/C]TTTTTAGGGTGAGAA | 5521 |
rs377570881 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693902 | GCACATCCTATTTCT[C/T]ATCTGTAACACTGTC | 5521 |
rs377571050 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629917 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTACCTCAG | 5521 |
rs377584207 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835738 | TCCTCTCCAGCTTAC[A/G]CTGTACTGTACAGAT | 5521 |
rs377586538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811066 | TGGAGTGCAATGGTG[C/T]GATCTCAGCTCACTG | 5521 |
rs377623553 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878110 | GAACCAGAAGCCGGC[A/G]GACAAGTATCCATGA | 5521 |
rs377623905 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877818 | TGCTGCTGAACGCCG[A/G]GCTCGCCTCGCGGAG | 5521 |
rs377635422 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601969 | TCACAAACTGCCTCT[A/C]ATTCTTTCTACCTTG | 5521 |
rs377653286 | snp | C/T | 0.000263827 | 0.0114823 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697938 | AGTATATAGTTTGGC[C/T]GACTGTATCTCTGAA | 5521 |
rs377671378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722617 | GGTGAAATCTTATTG[C/G]CTGACTGGTTTTTCT | 5521 |
rs377671496 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741428 | AATTATGAACTGACA[C/G]TGCTGCATATTCATA | 5521 |
rs377672309 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795394 | TTTGTGACCACATGG[A/G]AGAACCTAATACATT | 5521 |
rs377676986 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814969 | GAGGAGGCAAGAATT[A/G]AGGTTGCTGTAGACC | 5521 |
rs377689513 | snp | A/C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989375 | GCAAAACTAATTCAA[A/C/T]AACACATTAGAAAGA | 5521 |
rs377690624 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968325 | ATTTATGTACTTGTA[A/G]ATTGACAAATCTTGT | 5521 |
rs377703906 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147065853 | AAAATGAAAGAGTTT[A/G]TGGGGTGCCTGCTGG | 5521 |
rs377733236 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071994 | TGTCCTATGCCCTGC[A/G]TTTTCAAGACAGTCA | 5521 |
rs377737582 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025984 | ACTTTCTCTACCAAA[C/T]GGTAGTGAGAATGCT | 5521 |
rs377738820 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985935 | AAACTATACAAAAAA[C/G]AAATCAAGAGAACAG | 5521 |
rs377740199 | in-del | -/CAAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725051 | TTCTATTAATGCGAT[-/CAAT]AATTCATAGAAATTC | 5521 |
rs377740383 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007263 | AATTCCCAACAGCAG[C/T]TGGGGTGTCCTGTTT | 5521 |
rs377742788 | in-del | -/CT | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865816 | ACATCACACAAGACT[-/CT]GCCTCCAATGAGGAA | 5521 |
rs377743960 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988414 | TTGAAATCATATCAA[C/G]TATCCTTTCTGATCA | 5521 |
rs377752714 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875641 | TTGGAGGAAAAAAAA[-/A]GAACAATCTGACATA | 5521 |
rs377765706 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647031 | ACTCTGAAGCCTGAG[C/T]TCTCAACCGTAATGC | 5521 |
rs377766628 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635332 | TATTACATAGCTAAA[C/T]ATGTGTCATGGGTTT | 5521 |
rs386405234 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146663489 | TAAATAACAATATAC[-/C]AGGCATGTCCCAGAG | 5521 |
rs386405235 | in-del | -/TA | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866637 | TACATACATATATAT[-/TA]ACACACACATATATA | 5521 |
rs386693280 | in-del | CAATGACATATCTTCA/GAGTGACCGAGTATTACGGAGAAAGGCAATGACATATCTTCACTGT | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590248 | GGCAGAGAGCAAAGG[lengthTooLong]CTGTCTTTTCTTTTT | 5521 |
rs386693281 | in-del | CCACTACA/TAAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626133 | TAGTGTTGTTTTAAG[CCACTACA/TAAG]TTTGTGAGAATTTGT | 5521 |
rs386693282 | in-del | ACCC/CT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634782 | CACACACACACACAC[ACCC/CT]CCTACTGGTTCTGTT | 5521 |
rs386693283 | in-del | ATCTTTGTTGTCTGCT/GCCCTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677044 | AACTCCTGAACTCCT[ATCTTTGTTGTCTGCT/GCCCTG]TTGTCTGCTTTGACG | 5521 |
rs386693284 | multinucleotide-polymorphism | ACA/GCC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678342 | TGACAAAATTCAACA[ACA/GCC]CTTCATGCTAAAAAC | 5521 |
rs386693285 | multinucleotide-polymorphism | AAA/CAG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682592 | GCAAAATGGGAATAA[AAA/CAG]TAGTACCCACTCCAC | 5521 |
rs386693286 | multinucleotide-polymorphism | AA/TC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700670 | TAAACTATGTTTTTT[AA/TC]CTCCTGCATATTCTG | 5521 |
rs386693287 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715164 | CAAGATTTACAGACA[CA/TG]TTGTAAATGGCCAGA | 5521 |
rs386693288 | in-del | A/TTG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724325 | CATAGGTTTTTTTTT[A/TTG]AGGGTTACATGAGAA | 5521 |
rs386693289 | in-del | ATC/TT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756959 | GAGGAGGCAGACAAA[ATC/TT]AAGATTAAGGAGGGT | 5521 |
rs386693290 | multinucleotide-polymorphism | GT/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780059 | AAACAATGATGTAAC[GT/TG]GGGGTTAAATTTTTC | 5521 |
rs386693291 | in-del | G/TCCCAT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798019 | TTTCAGAGTCTCCCT[G/TCCCAT]AACTACTCCATCCGA | 5521 |
rs386693293 | multinucleotide-polymorphism | AT/GC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839379 | TACAAAATTAGCCGG[AT/GC]ATGGTGGCATGTGCC | 5521 |
rs386693294 | in-del | ATATACATAACAAACATTTA/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840227 | ATTGAGTTCCCTTGA[ATATACATAACAAACATTTA/T]ATTGAGTGACTCCTC | 5521 |
rs386693295 | in-del | A/CT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902833 | CAAAGTTTTGCTACA[A/CT]GGAATCAGTTTATTT | 5521 |
rs386693296 | multinucleotide-polymorphism | ACG/GCA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909681 | CTGTGTTGCAAGCCC[ACG/GCA]TGTCCTCTGTGTCAC | 5521 |
rs386693297 | multinucleotide-polymorphism | AA/GG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933654 | CCTATCGTGACAAAC[AA/GG]AAGTTCTTTTTTTTT | 5521 |
rs386693299 | in-del | ATAGTTCCATATTCA/GTAAAGTAAAGCC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989232 | GCTAAAGTGAACCGA[ATAGTTCCATATTCA/GTAAAGTAAAGCC]TTCTACAAGGCCAGC | 5521 |
rs386693300 | in-del | AACC/GATTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002554 | AGGGCCACTAAATCC[AACC/GATTT]TTCTCGGTCTTCTTT | 5521 |
rs386693301 | in-del | CTT/TC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002562 | TAAATCCGATTTTTC[CTT/TC]GGTCTTCTTTGTGGT | 5521 |
rs386693302 | in-del | ACGC/GT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053230 | AAAAAAAAAAAACAC[ACGC/GT]GCACACAAAAAAAGC | 5521 |
rs386693303 | in-del | AG/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069908 | CAATTCTCTTGCCTC[AG/T]CCTCCTGAGTAGCTG | 5521 |
rs397700854 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907218 | ATTACATTTTTTTTT[-/T]CCATCAGCAGATGTA | 5521 |
rs397703040 | in-del | -/T | 0 | 0 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914112 | TTTGAAAGTGGACTT[-/T]AGTGCATATGTAAAT | 5521 |
rs397704985 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041611 | GAAGTATTACACTTA[-/A]GAGTTTTTTCCTTAG | 5521 |
rs397708052 | in-del | -/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916307 | GTTTTTTTTTTTTTT[-/T]GACGACTCAGAGGAA | 5521 |
rs397715160 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977056 | AACAAAACAAAAAAA[-/A]CAAATCTGGAGTCAT | 5521 |
rs397722743 | in-del | -/T | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768902 | CTTTTTTTTTTTTTT[-/T]GAGACAGTCTCTCAC | 5521 |
rs397725464 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964448 | TTAGGATATTTTTTT[-/T]TATCTTGCAGGACCA | 5521 |
rs397736764 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991695 | ACTTGTACTCCCTAA[-/A]TATGTACAATTATTG | 5521 |
rs397740775 | in-del | -/A | 0.375 | 0.216506 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146746394 | AGTTTAAAAAAAAAA[-/A]GTCATATGTAGCAAT | 5521 |
rs397749065 | in-del | -/A | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940524 | GGAAAAAAAAAAAAA[-/A]CATAAGGCTACTGCC | 5521 |
rs397755460 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659046 | AGAAATGATCAAAAA[-/A]CCTTTTAACATGATT | 5521 |
rs397780702 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037167 | TTCAGGGAAAAAAAA[-/A]TTATTTTTGCCTAAG | 5521 |
rs397790031 | in-del | -/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914111 | CTTTGAAAGTGGACT[-/T]TAGTGCATATGTAAA | 5521 |
rs397794001 | in-del | -/A | 0.375 | 0.216506 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821789 | TGCCAAAAAAAAAAA[-/A]GCTTAATTACATGAA | 5521 |
rs397800612 | in-del | -/A | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022568 | CATCCAAAAAAAAAA[-/A]TCCAAATTTAATAAG | 5521 |
rs397803932 | in-del | -/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031488 | ATTGCTTTTTTTTTT[-/T]AATTTATCTTGACTG | 5521 |
rs397810071 | in-del | -/AC | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050689 | CACACACACACACAC[-/AC]GCATCCATACCTACA | 5521 |
rs397814677 | in-del | -/TA | 0 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866638 | ACATACATATATATA[-/TA]CACACACATATATAT | 5521 |
rs397825166 | in-del | -/TT | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954143 | CTTTTTTTTTTTTTT[-/TT]CAGTTTGGGGAGCCA | 5521 |
rs397832223 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699662 | TGCGAACTTAATTGG[G/T]ttttttttttttttt | 5521 |
rs397832299 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900558 | aaggaaggaaggaag[A/G]aaggaaggaaaaaga | 5521 |
rs397833106 | in-del | -/A/AG | 0.498833 | 0.024124 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808697 | CTCCTCATTTCTATC[-/A/AG]GGGAAAGAAAGTCCA | 5521 |
rs397837683 | in-del | -/TG | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954787 | gtgtgtgtgtgtgtg[-/TG]TTGAGTTGAGGGTAT | 5521 |
rs397841594 | in-del | -/C | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879298 | TGCAACTGGTTCCCC[-/C]ATTCCTAAGAGTCAA | 5521 |
rs397882297 | in-del | -/AC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053230 | AAAAAAAAAAAACAC[-/AC]GCGCACACAAAAAAA | 5521 |
rs397882538 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877144 | CACTGGGGGAAAAAA[-/A]TGCCTCTACTCTCTA | 5521 |
rs397882774 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936485 | GAAAAAAAAAAAAAA[-/A]CCCTAGACAGTTATG | 5521 |
rs397883054 | in-del | -/AC | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915473 | CACACACACACACAC[-/AC]GTACACATGTGTGCA | 5521 |
rs397883078 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680593 | CACTTAAAAAAAAAA[-/A]GTTCCCAGAAATCCT | 5521 |
rs397883165 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642149 | AGGAGGGGGCATAGC[-/C]AGCTTGGCAGCTGAG | 5521 |
rs397883304 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886824 | CATTTTAAACTTTTT[-/T]AGTAAAAAAAAAAAA | 5521 |
rs397883592 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831523 | AAAAAAAAAAAAAAA[-/A]GCCTCTGGGTTGATA | 5521 |
rs397883786 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993818 | CACAGTTTTTTTTTT[-/T]AAATAAATGTAAGTC | 5521 |
rs397884440 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941512 | GATGCTTCTGTTGCT[-/T]AGGGGTGTGTTCAGA | 5521 |
rs397948355 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956242 | CCATTCAATTTTTTT[-/T]CATATTAATTATTAC | 5521 |
rs397949374 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051780 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAT | 5521 |
rs397957859 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999038 | AAAAAAAAAAAAAAA[-/A]GAGTCAATCTCTGGT | 5521 |
rs397966254 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830542 | GCTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 5521 |
rs397969628 | in-del | -/TCA | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686625 | AAATTGTATTCATCA[-/TCA]CATCACCTTCATTTT | 5521 |
rs397971675 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635353 | CATGGGTTTTTTTTT[-/T]GTGTGTTTATTTCAT | 5521 |
rs397999524 | in-del | -/TGTGTGTG | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740616 | TCAAGAACTTTTATC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 5521 |
rs398050829 | in-del | -/ACAC | 0.5 | 0 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865326 | CACACACACACACAC[-/ACAC]TGAGCCTGGAAGGAA | 5521 |
rs398093796 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673493 | AGAAGATTTTTTTTT[-/T]ATTGCTACTAGAAAA | 5521 |
rs398093797 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897818 | AATAAGAAAAAAAAA[-/A]CATGGAATTAAAAAA | 5521 |
rs398093798 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054493 | CAACTGTAAAAAAAA[-/A]GTCCATGAGATATCA | 5521 |
rs398109518 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667584 | TACTTAAAAAAAAAA[-/A]CCCAAAAGGATTACT | 5521 |
rs527236725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146724924 | AAAGGGAGAACACCG[C/T]TCAATAGGGTTTTGA | 5521 |
rs527238998 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049887 | GAGTGTGGATGACAC[-/T]TTCAAGGCATTTTTC | 5521 |
rs527239355 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645540 | AGTTCCCCTGGAAGC[C/T]TGCCTGGCAGAATCC | 5521 |
rs527242586 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863979 | GAAAAGGGCCATAGC[A/C]ATTACAAAGGTATTC | 5521 |
rs527246114 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786064 | GAAGGAATAATAAAA[C/T]CTTTGAGGTGATGGA | 5521 |
rs527251186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146857102 | TGGACAGGATACTCA[A/G]CGTTTGGGGTAGGGT | 5521 |
rs527264120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772227 | TTATCCCCTAAAACA[A/G]CAAACATTTATAGAT | 5521 |
rs527269839 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994480 | AGAAAGGAACAGAAG[A/G]CCCCCAGTGAATAAT | 5521 |
rs527276496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779573 | CTGAAGCATGCTGGG[C/G]AGAAGATAAAATTTA | 5521 |
rs527288118 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632072 | TTGTGCCCCCCCCCC[C/G]GCCCATTCATATATT | 5521 |
rs527288521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038834 | GTGGTCTGATCTAGG[A/G]CCAAATTATCCCCTT | 5521 |
rs527295968 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848875 | TATTTATTCAATTAT[G/T]TACTTATACCAGTAT | 5521 |
rs527296316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730964 | AACCGATGAGGCCTT[C/T]GAGGCTCACAGTGGA | 5521 |
rs527311232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902031 | GATGAAAAAATCTCT[A/G]AAGAGCTGAAAGCAC | 5521 |
rs527311951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908651 | TTTCAGGTTGTAGTT[A/G]AAGAAGGTGATGACC | 5521 |
rs527327724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146863493 | AGGAAGAGGATGAAA[A/C]GTAGATTTTAATATT | 5521 |
rs527330413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778736 | CAGGGGTAAATGACA[C/G]AGTCATCAGAATACA | 5521 |
rs527332784 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765614 | ATAATCAAGACCATG[A/C]TTTGTTTCTTAACAT | 5521 |
rs527339403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688285 | CAAATATAACATGTC[A/T]CTCCAAAAAATAACA | 5521 |
rs527347016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970695 | AATTTACAAAGGAGA[C/T]GGTAAAGGGAGGTGT | 5521 |
rs527347106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032065 | CTAATTAAACTAAAG[A/G]GCTTTTTGTACAGCA | 5521 |
rs527365973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812923 | CCCCATGATTCAGTT[A/G]TATCCCGCTGGGTCC | 5521 |
rs527367322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644356 | CCCTGAACCCACATT[A/G]TTGAATTAGCTAGCA | 5521 |
rs527369469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990858 | ACTCAATGATTCAAT[A/G]GCAAAAAAAGAAAGA | 5521 |
rs527369581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983932 | GTCTTAATTTTCCCT[A/T]TATTCTTTCTAAACA | 5521 |
rs527376701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075711 | AAAACCTGAAAACTA[A/T]CTTAATTCCTTAGTT | 5521 |
rs527376886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146896957 | GAAGGTAATGATCCT[C/T]CTTGATTTAGAACAA | 5521 |
rs527384865 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937727 | CAAGGAGCTGCAGGT[C/G]GCTCGGTACAGCTCT | 5521 |
rs527402814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857605 | AGATTAAGGTTAGTG[C/T]ATTAACTTATTTGTC | 5521 |
rs527406118 | snp | A/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615620 | CTCAACAGCAAATAA[A/T]CTCAAGAAATTAAAC | 5521 |
rs527407405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595360 | TAGTTCCATATGTCT[A/G]CTTTGTGATGAACCT | 5521 |
rs527412331 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082454 | CCCATCTCTCAGAGT[C/T]GTGGATGTTGAATAT | 5521 |
rs527412582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941390 | AAAATTATGACAAAC[C/T]GGCCTGAAATTCTTT | 5521 |
rs527418339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773100 | CCTGTAATAGTGAAG[A/T]TAAAGTTAATCCAGT | 5521 |
rs527423501 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755903 | AGTGGAATTGGGTCC[A/G]GAGCTTAGCTGCAAA | 5521 |
rs527428138 | snp | A/G/T | 4.95678e-05 | 0.00497814 | synonymous-codon, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146638273 | GTGCCTGTCACACAG[A/G/T]GCAGATGCCCGCATG | 5521 |
rs527452485 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884395 | GGTTATGAAATTGCC[A/G]TGGTAGACTTGTGAG | 5521 |
rs527459616 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725469 | AAGCTAGGATATGCA[C/T]GCATGCATCTAAATG | 5521 |
rs527470503 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775617 | ATAATACTGAAAGAC[C/T]TAGCCAGAGCAATTA | 5521 |
rs527472360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025152 | GTGGGTATTATCAAC[A/C]ATTTTATGCTAATGA | 5521 |
rs527478353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619599 | TTTTGAGGAACTCTA[A/G]TTTTTTCATGTTAGC | 5521 |
rs527478734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702465 | GATAGCAAATACAAA[A/G]GCCTGCAGGGCCACA | 5521 |
rs527480491 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845485 | GTCTTGATCTCCTGA[A/C]CTCGTGATCCGCCCG | 5521 |
rs527481825 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146630188 | CTCTATTCTTTGAAC[A/T]CACAAGTTTCCTCCT | 5521 |
rs527491593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890869 | AGAATTTAATGATTT[A/C]TCTCCCCAGGAAAAC | 5521 |
rs527497047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807325 | TGGCAGTATGTTTTT[A/G]CTTATAGGTGTACTT | 5521 |
rs527507789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984630 | AATCATATGGTAGTT[C/T]TGTTTTTAACTTTTA | 5521 |
rs527512268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942077 | ACAACAGTTATATTG[A/G]ATCAGGGCCCACTCT | 5521 |
rs527516111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664478 | TACCATGAGGCTGCA[A/G]CAATTAAGACCCATC | 5521 |
rs527530118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977582 | TCACTGTGTCCATGT[A/G]TTCTCACTGTTCAAC | 5521 |
rs527531981 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668667 | TTTTTCTGCAACTTT[A/G]CTTTGGCTGTGTTTC | 5521 |
rs527542247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970727 | GTGGTGAGGAACTTG[C/T]GGCTCATAAGAAGGT | 5521 |
rs527548984 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062060 | ACATTTCAGTCAACT[A/G]TGGACTGCAAATATG | 5521 |
rs527556638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717159 | GTTCATTGCTATAGG[C/T]TTATAGCCTGGGACA | 5521 |
rs527557865 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601571 | AGAAATAAAAAAAGT[G/T]GTGCTTTCTTACTGG | 5521 |
rs527558618 | snp | A/C | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911235 | ACAACAGGTGCACAC[A/C]ACCATGTCCGGCTAA | 5521 |
rs527559816 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883831 | TGCCCTCAAAGTGTT[G/T]TATTAATTCTAGACT | 5521 |
rs527563335 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632888 | GTGGCCAGGCTACAG[C/G]GAGCTGAGCCTGGAA | 5521 |
rs527566876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885044 | TGCCCAACAAAATAA[C/T]TTGTTAGGCAAATTA | 5521 |
rs527581792 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994792 | TTACTTTAATGTATC[A/G]TATACTCAGCACTGT | 5521 |
rs527587644 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670540 | TTGCTCTGTGACCCA[A/G]GTTGCAGTGCAGTGG | 5521 |
rs527592674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838891 | GAAATCTGAAGCAGC[A/G]TTAGAGGTTTAGCCC | 5521 |
rs527605046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849710 | CAGTAATACATCTAA[A/G]CCATGCAAAAAGGAT | 5521 |
rs527607615 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978102 | ACCTCATTCTGGTTT[C/T]GGTTTGCACTTCTCT | 5521 |
rs527617171 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778122 | TTCCAGAGGCAATGG[-/A]AAAATGGCAATTTGG | 5521 |
rs527621691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625274 | CGATTTAATTTTAAT[A/G]TTCATGTAAGTTAAA | 5521 |
rs527623328 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884530 | TAGTCTTGCCCTTGA[C/T]TTGCTTCAATACTAA | 5521 |
rs527637620 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024839 | GAAGAAAATTTATAG[A/C]TTTAAATGCTTATGT | 5521 |
rs527640644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010347 | GGTTCAAGTGCATTA[C/T]ATTTATTGTGCACTT | 5521 |
rs527642569 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852371 | CTAACAAATCATAGC[C/T]TGATTACAGGTCATT | 5521 |
rs527650091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786869 | ATTTTCTTTAATTCA[A/G]TCATCTCAGGAAGCT | 5521 |
rs527670345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689272 | ACTATCATCATCCCC[A/G]TTATATAGATGAGAC | 5521 |
rs527673562 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843904 | TGAATAGTGCCGCAA[C/T]AAACATACGTGTGCA | 5521 |
rs527673624 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763499 | GACATACCCAACACA[C/T]GAACTGACTCTTGGC | 5521 |
rs527675173 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670910 | TTGTCAAAAAAGAAG[A/C]AAATTATAAAAATAA | 5521 |
rs527701543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019130 | ACTTAGTTAGAAATG[C/T]AGATCTTCTGGTACA | 5521 |
rs527702469 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037960 | GAGGGAATGAGTAAT[A/C]AAGTTATATAATGTT | 5521 |
rs527704028 | in-del | -/ACAT | 0.0228947 | 0.104514 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077283 | TGTGTATACACACAC[-/ACAT]ACACACACACACACA | 5521 |
rs527710594 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805898 | CGATGAGTCTGACTT[C/T]CTAGTTCTTATTTAT | 5521 |
rs527711944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055366 | GGTTCCAATGACTTG[C/T]TTGCATGTTAAATGA | 5521 |
rs527713316 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648018 | AAAGCCCTTGGAGAC[A/G]GTTGAGTGCTCTCCA | 5521 |
rs527713469 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620285 | AATATGTACAGACAA[A/G]TTCATTAATTGTGGG | 5521 |
rs527713950 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596559 | TTTGTCCTAAATCTA[C/T]TCTTCCTAGTTAAGG | 5521 |
rs527715116 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793686 | AGAGTCTGTGTTCCT[G/T]TCACCCAATATTGCT | 5521 |
rs527722162 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971537 | TCCAATCTTTTTCTA[A/T]GAGAAATAATGCTAT | 5521 |
rs527728369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964042 | TGTAGGCCATCCAAA[G/T]GTAGCCCTTAAGTCA | 5521 |
rs527733418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684516 | ACCTGGCCCCTCAGA[A/G]CCAGTTACCCTCTTT | 5521 |
rs527740036 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002192 | CCAGGACTCTGTTAC[C/T]TTCTTTAGGCACCTG | 5521 |
rs527745951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694662 | GTAATATTGCATATA[C/T]AGATTTTGTATTTTC | 5521 |
rs527746354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146703213 | CTTCCAAATTTGGGT[A/T]CAGCCTAAAGCGGGC | 5521 |
rs527747486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910149 | GCCTAGCTATTTACA[A/G]TTTGAAGTCTAACAT | 5521 |
rs527748788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608438 | ACGCAACTTATCTTT[A/C]AAATGTAGACATCAA | 5521 |
rs527766157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146872412 | TCTGATCTGGCATTT[A/G]CATACAAATACCAAA | 5521 |
rs527770289 | in-del | -/TTATTATTATTA | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976109 | CATTTTTTAAAAAAT[-/TTATTATTATTA]TTATTATTATTATTA | 5521 |
rs527778875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657433 | TGGATGGATTTTAGC[C/T]GTTTAGTAACTCTAG | 5521 |
rs527779699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651621 | CTAATGCCTGAGAGG[C/G]AACAAACTAAAAAAA | 5521 |
rs527785914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780225 | TCAAAATCAGAGAAG[A/T]AGTACATGTTTAATA | 5521 |
rs527791116 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693196 | CTTCCCTTCCTCTCT[C/G]CTTTCTTCCCTTCCT | 5521 |
rs527792242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602017 | TAGAGTATATCTCGA[C/T]ATTTCCCACTTCTAT | 5521 |
rs527795784 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787773 | GGGTTTCACCATGTT[A/G]GTCAGGCTAGTCTCG | 5521 |
rs527797212 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787600 | TGAGATGGAGTCTCA[A/C]TGTGTCACCCAGGCT | 5521 |
rs527826075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834114 | AATGCTAAAAAGGAT[G/T]CTTGTTATTTATGAT | 5521 |
rs527829922 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004249 | CATCCATGTCTGCTA[C/T]GCCGAGGCAATCACT | 5521 |
rs527831907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909350 | GGATTTTTATTCCAA[C/T]CCCAATACACTTCAA | 5521 |
rs527833204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827384 | GATCAAGGCATAGAG[C/T]AAGGTAAAATACAAT | 5521 |
rs527842907 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594358 | AAGGCTCATCAAGCA[C/T]AGTTGAATATTTTTC | 5521 |
rs527846684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590594 | GAATGTGAGACTAGA[A/G]TGAGGTTTGTCGAAG | 5521 |
rs527861330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678125 | GTGGTTAAGAGAACA[C/T]TGATGCAAAAATCCT | 5521 |
rs527871066 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951363 | CTTTTTTTTTTAAAA[A/G]TTAAGTTCCAGTGTA | 5521 |
rs527872035 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975485 | TATGCAAATATGTCT[C/T]TGAGATCTTGCTTTT | 5521 |
rs527887937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033217 | GTTTGGTCCTGGGCC[C/T]CCTTCTATTTTCAAT | 5521 |
rs527889665 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951091 | TCACTTACCACTTGG[A/C]AGTTCTTCAAATTCA | 5521 |
rs527889911 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729542 | CATGACAGCCCCTCC[A/C]ATCACAGGCCCAGAG | 5521 |
rs527894430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732421 | AAGTGAAAACCAATG[A/G]GAGGATGGACAAAAA | 5521 |
rs527906712 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943532 | AGGGTTAATCTTGAC[A/T]CCATTTTAATGTGTT | 5521 |
rs527912576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903905 | AAGCCAGAGTTGGCA[C/T]ACAGTACCAAATGGT | 5521 |
rs527921803 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671784 | TTTCTTCTATTGTAT[A/T]ACCTGCTATTGCTAT | 5521 |
rs527925390 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146865803 | CTTTTGCCTCCTAAC[A/T]TCACACAAGACTCTG | 5521 |
rs527928108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780958 | GCTTTGTAAAGATAC[A/G]GTTTTCAGTGCCAAA | 5521 |
rs527930906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760797 | AAATTGCTGTTGAAG[C/T]TTACCAGGGGTATTG | 5521 |
rs527931047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767965 | TTTCCAGAGCCATAT[A/G]TTTTTTAAAACAATT | 5521 |
rs527946694 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946179 | GGACATACAATTAGC[G/T]AGTAGCGAGTATAGC | 5521 |
rs527950468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034046 | CATATATGGCCTAGC[A/G]CCTACCTTCCATACT | 5521 |
rs527952429 | in-del | -/A | 0.402454 | 0.198136 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708356 | GCCAGACTTGGTCTC[-/A]AAAAAAAAAAAAAAC | 5521 |
rs527963754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078164 | CTGTCATAAGGTTTT[G/T]GTGAACACTAATTTA | 5521 |
rs527966575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639706 | TGCCCTATCTGTGCA[C/T]CATCAGATAGTACTT | 5521 |
rs527967129 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671141 | AATTATGTGATTCAA[C/T]ATTACTTACAGTTGT | 5521 |
rs527967361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815376 | GTATGCTTATTGAGA[A/G]CAGAGAGGCCATCTG | 5521 |
rs527973592 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898497 | ATTAAAGACTTGAAC[A/G]TTAGACCTAAAACCA | 5521 |
rs527980491 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146985471 | GTCAAATTCAAAAAA[G/T]TATTGCCTAAACCAA | 5521 |
rs527996155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677689 | TGCACCACCATGCCT[A/G]GCTAACTATTGTATT | 5521 |
rs528010499 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852836 | AAGTGACAGGAAAAA[G/T]GTCTATTTGACAAAA | 5521 |
rs528020636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898021 | AAAACCCCGTGTCTA[C/G]TAAAAGTACAAAAAT | 5521 |
rs528021922 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640336 | GTCTCCTGGATTCAC[A/G]AAATACTACCCTTCA | 5521 |
rs528025135 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885384 | CACAACAGAATCACC[G/T]GGAGGTCTCTTTCCA | 5521 |
rs528030818 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732155 | ATCACCACTCATTTA[C/T]TCTGCTTCTAACTTA | 5521 |
rs528031389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802760 | GATGGGATAAGTATA[C/T]AGTGAGGTCTTTCCA | 5521 |
rs528068184 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938028 | TAAGCAGTTAGCAAG[A/G]GCAACTGGTCCCAGA | 5521 |
rs528072297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609605 | TCTCACTAGGGAGTG[C/T]CAGACAGTGGGCGCA | 5521 |
rs528072928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847289 | ATTCAGCCTTTAATT[A/C]CTGACATAATAGACT | 5521 |
rs528076108 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146720529 | AGATGCTGTTTCTTG[G/T]GGGGAAGATGTCGAA | 5521 |
rs528081278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892793 | TAAAACTTCTGAGAA[A/G]TCCTGCAATAAAAAA | 5521 |
rs528082658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027752 | GTGGTGATGATCAAT[A/G]GGAGTATATATGTGT | 5521 |
rs528086037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621210 | CTACAGGAAAACACT[A/G]CTCCTAATCCACTGA | 5521 |
rs528090363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027211 | ATCCATTTATATCAA[A/G]TTCTACAAGGATAAG | 5521 |
rs528108129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658775 | ATTCATAAACATTCC[C/T]GAGAGGGACATTTGC | 5521 |
rs528109698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146936567 | AGATTTTTACAGTCG[C/T]TTTGATTGCTTTTCA | 5521 |
rs528111657 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697884 | AAGTTTTTCAACAGC[C/T]CACACAGTTCAAAGG | 5521 |
rs528111727 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809112 | ATGGATCCAATGTCA[C/G]GGGCTTTGGGGGCAG | 5521 |
rs528114428 | snp | G/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916767 | CTCAGTAGTTTCAAT[G/T]TTGTGACTTGTAGTA | 5521 |
rs528114550 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725217 | CTTCTTTTGAGTACC[C/T]GACTGTATTTTGCTC | 5521 |
rs528117135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078516 | GTATTGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 5521 |
rs528135562 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973002 | GTAATAAAATGTATT[A/C]GTTTCTCTTATGAGT | 5521 |
rs528142815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650440 | AAGGGGCAAGTTCTC[C/T]GCAAATGCTAGGTGT | 5521 |
rs528147296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965638 | GCCCCGCTTGCTTTG[C/T]GTCAGCTTCCAGGTG | 5521 |
rs528147669 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692847 | CCTAATTCAATTATT[C/T]AAGGAGACAAGATCA | 5521 |
rs528151357 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660316 | TCATTTTAAAAAATA[C/T]GCATCTTAATTCCAT | 5521 |
rs528153003 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892675 | AATGGCACAGAATCA[A/G]TGTCTTTTGAGGCAT | 5521 |
rs528157628 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880420 | AGCTGTATCTATCAC[C/T]GAGGTTCCAACATTC | 5521 |
rs528163066 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795411 | GAACCTAATACATTA[C/T]GCCAAATGAAATGAA | 5521 |
rs528167364 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729100 | TGAATGGCTGTGTCC[-/A]AAATGCTGATAGCGA | 5521 |
rs528170389 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835035 | CCACCACTGATGGGC[A/C]CCTAGATTGATTCTG | 5521 |
rs528196861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146924005 | CAGCATGTTCTCATA[A/C]GTGGGAGCTAAATGA | 5521 |
rs528202052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753625 | ATGTAAGGAATTCGG[C/T]CTGATGCTCGGTTTT | 5521 |
rs528202223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020896 | GAAAGTATTTTAGTT[C/T]GAGAACTGTATAACT | 5521 |
rs528207314 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075456 | TGCCAAATACCATCT[-/G]CATGCTGAGGCCTCC | 5521 |
rs528211116 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974369 | TTCACACATTAGAAA[A/G]TGGAGGTCCAAGGAG | 5521 |
rs528213363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146972538 | CCAACATGCTGAAAC[C/T]CCGTCTCTACTAAAA | 5521 |
rs528223065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005466 | CCCATGCTGCAATAT[A/G]GAAAGAAAGGGAGTT | 5521 |
rs528228490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873913 | TTTATCACTCTTCTC[A/C]CTGTTCCTAGCCATA | 5521 |
rs528230946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146711607 | CAGGTAGGGTCCTAC[C/T]TGGGAGAGGGCATGG | 5521 |
rs528231952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647149 | CTTTACATACACTTA[C/T]TTTGTAATCTAAATA | 5521 |
rs528236912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931045 | ATATTTTGTTTGCTA[C/T]TGTGCCAAAGATAAT | 5521 |
rs528238499 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146909307 | GAGCAGTTCTTGAAT[C/T]CAGTTCATTTGCTTC | 5521 |
rs528245410 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832820 | GGTTTATAGTCCAGG[A/G]GCAATAGCCTATACC | 5521 |
rs528248782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653716 | AGCTGCCAGCCCACA[C/G]CTTCAGCTTAATGTG | 5521 |
rs528249704 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147046996 | CTTAATCTGACACCA[A/C]CACCACCAAGTTTCA | 5521 |
rs528256592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918547 | AGGACTTCCCATTGC[C/T]TTTAGGATAAAGTCC | 5521 |
rs528267452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874274 | GAACATCCCGTATCA[A/C]CTCTGCAAAACGTCA | 5521 |
rs528275460 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899009 | GGAGAAATAGGAACA[-/C]TTTTACACTGTTGGT | 5521 |
rs528275627 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690958 | TAGAAGGCTTGGCAC[A/C]TTTCCTGCTTCTCCA | 5521 |
rs528275869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828564 | TCAGCTATTAATAGC[C/T]GCTGGTACACACTTA | 5521 |
rs528280414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959674 | AGGTGCTTGAACTGT[A/G]CTGAAACTGAAGAAG | 5521 |
rs528280465 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835514 | TACTGAACTTGGGGC[A/G]GAAAGATCACTGCTT | 5521 |
rs528284714 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057763 | CTTAAGAGGAGTGAG[G/T]CTGCAGTTAGACAGC | 5521 |
rs528285599 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050387 | TGGAGGTGCATTTGA[C/T]GTGGGCTGTGAAGAG | 5521 |
rs528287115 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011482 | TTGAAAGTATTATGT[A/G]AAATTACCTTCAGAC | 5521 |
rs528290331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747239 | GTAGGCAGTTTAGCT[A/G]TGAGACCATCCTGGG | 5521 |
rs528298032 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629868 | GCCTAGGCTAGAGTG[C/T]AGTGGCACAATCTTG | 5521 |
rs528304291 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008047 | CTTTGGATCGATTCT[C/T]CTTATTTATTGAACA | 5521 |
rs528308383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647901 | ATGTGGAGTCTGTTC[C/T]GTGATCAACAAAATA | 5521 |
rs528314385 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880878 | CAGATTGGATAGGTC[C/T]CCATTGTTTAAGTAG | 5521 |
rs528314898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795849 | AAAAACAGAAGATTC[G/T]ATGGAATAACGCACA | 5521 |
rs528316034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686291 | GAGGAGGCAGACAGC[A/G]AAGAAAATGCTAGAC | 5521 |
rs528321546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057034 | CTTGAAAATCTGATG[C/G]AATAATTTTTAAGCC | 5521 |
rs528326108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051386 | GCCAGTGGTCCACAG[A/G]GTTCATGGTGCTGAA | 5521 |
rs528326142 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010766 | CTGTGGCCTGGGAGT[C/T]GGGGACCCTGATCTA | 5521 |
rs528326446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146905690 | CACTCCTATTAAATA[C/T]CCTCTAAATAAATCT | 5521 |
rs528328478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912195 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 5521 |
rs528330957 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873410 | AAAACAAATCTGATC[A/G]TGTTTCCCTTTTCCT | 5521 |
rs528336563 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632315 | ACTGATCCTTCTTTC[A/G]TAGCCTCCAGAAGAA | 5521 |
rs528339071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042515 | TTTATGGTAGCTAAC[A/G]TTTGGAAACTACTGT | 5521 |
rs528340114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146823152 | TCTGACAGCCTGCAT[A/T]TCACTACCTATGGTG | 5521 |
rs528362874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639109 | TTGCTTCAAGTCACA[C/T]GGCTAAGTGACAACA | 5521 |
rs528363010 | in-del | -/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078611 | GCTAACACGGTGAAA[-/C]CCCATCTCTACTAAA | 5521 |
rs528367953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993301 | AGGCTAGAGTGCAGT[A/G]ACACCATGTTGGCTC | 5521 |
rs528368298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952352 | GCATCCTGCTGGGGC[A/G]CCTCTTTTCCATCAC | 5521 |
rs528379136 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604137 | GAGGAGGGGACAAAT[A/G]TTTAGCAATCACACA | 5521 |
rs528382703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835431 | CAGGTCAGTTGACCT[A/G]GGCCCCACCCTCATG | 5521 |
rs528395221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867474 | TATTGGTCCCAAATG[C/T]ATGGAGTAGAGAGGG | 5521 |
rs528399545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690476 | TCATTTGTATATTAG[C/T]CTTACAAATCCTCTT | 5521 |
rs528423213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829012 | TAGAGAAGAACGGGT[A/G]AGTGAGCTGAATAAT | 5521 |
rs528427808 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000441 | CTGTAAATGTGTTCT[G/T]CCATTTACAAGCTAT | 5521 |
rs528429372 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592873 | GGTTTTGGGGCCCAA[G/T]TTTGACCTCCCTTTG | 5521 |
rs528438058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681075 | TACATCAATGCATCA[A/G]TCGAAGCCCGGCTTG | 5521 |
rs528438614 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146740404 | TAGAGGTGTAAATAA[A/G]GAGCTTTGAAACCAC | 5521 |
rs528443375 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994062 | AAGGTCAAGGCAGAC[A/T]GTCAAAAAACCTCTT | 5521 |
rs528443930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035702 | GGAGAGAATGGAAAG[A/T]GAAAAATAGTTAAGA | 5521 |
rs528445396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673373 | AATAATGAACTTGTG[C/T]TGGAAGAAAAGATTA | 5521 |
rs528462359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776360 | TCATCTCTATGGTCA[A/G]ATGATTTTCTACAAG | 5521 |
rs528463145 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768866 | CTTAACTATCTTATC[A/G]TCAGGCAAAGATTTG | 5521 |
rs528471785 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146945789 | TCATTGTGTAAGGCA[A/G]TTCGATTTGAGAAAG | 5521 |
rs528488133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628999 | TACCCCATTGGTAAA[C/T]GTCGGTGTGGCCTTC | 5521 |
rs528491762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043442 | GTTGAGAAGACGGTC[A/G]TCAGCAAGCCAAGGA | 5521 |
rs528506522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635908 | GGGGAATGACATTGA[A/C]CAATTCATATCACGT | 5521 |
rs528515461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775742 | AAGAACACAAACACA[C/T]ACACGCAAATCTGTC | 5521 |
rs528524990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860608 | TAGGTCCGATAGTCA[C/T]TAATCCACTGACTAA | 5521 |
rs528528089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147036509 | ATAATAGAACAATTT[A/C]TATTCATTTGGGTAT | 5521 |
rs528535122 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656742 | AGTAAGGAAGCATGG[C/G]AGTTGGAGAAGATGT | 5521 |
rs528542351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810376 | AAAACCATCAGATTG[C/T]GTGAGACTTACTCAC | 5521 |
rs528558567 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922542 | CCACAGCACATGGGG[C/T]GGGGAGCTCAGGGTC | 5521 |
rs528572772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680572 | AAAAAACCACAGCGT[C/T]GCACACACTTAAAAA | 5521 |
rs528576072 | snp | A/C | | | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589204 | CAGATGGAATTTGGC[A/C]CCGCCTGGCCCTGCC | 5521 |
rs528576979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146721823 | GTAGCTCTTGCAACA[A/G]CCTTGCAGGATAGGT | 5521 |
rs528587901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981418 | AATCTATTACTTAAA[G/T]AATTTTTTTCTGGCT | 5521 |
rs528598670 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925950 | TTAAATTACCATTAT[C/T]GTACCCTTCAGCTAC | 5521 |
rs528600364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029096 | TTTCTACACTGTGTC[C/T]TGCCTTTTTAGTCTT | 5521 |
rs528600767 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854785 | AGGGCACTGTCTTTG[C/T]ACTTTGAAGGGATTT | 5521 |
rs528602448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146817142 | AATTCATGTTGCTAC[A/G]TTTGGCCCATCATCT | 5521 |
rs528603689 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592392 | CTGGTAGCTTGCACT[G/T]AGTTCTCATGGAAAT | 5521 |
rs528604192 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705122 | ATCAATCATAGAGAT[A/G]GAAATGCAAGGGTAA | 5521 |
rs528611192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079594 | TAAGCCAGGCACAGA[C/T]AGACAAATACCACAT | 5521 |
rs528611405 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938185 | CTATCAAAAAAGAAA[A/C]AATCCTGTTCATTAA | 5521 |
rs528615944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953707 | CACTGAGCCCTTCAA[C/T]AAACACAATCTCCAT | 5521 |
rs528618382 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925286 | TAGAGTACCATTTCC[A/G]GAAGGCCTTCCTTCC | 5521 |
rs528643865 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061737 | CTCCATTTAGAGCAG[C/T]TGCTACCATGCAGCA | 5521 |
rs528644519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635489 | CCAGTCAGTTGATTC[C/T]CCAATATCCAGAATG | 5521 |
rs528655459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842373 | CCTATATTCTAAATC[C/T]ACCACAGTCAACTTG | 5521 |
rs528662569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029743 | CACCAAGAGTGGGCA[C/T]GCATAAAGGAAAGGC | 5521 |
rs528667171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146888831 | CTTTCAGACACCAGC[A/G]TAGCTCAGTGCTTTA | 5521 |
rs528667647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022340 | GAGGTGGGTGGATTA[C/T]GAGGTCAGGAGATTG | 5521 |
rs528673720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698954 | GGAAGAAAAAGAAGA[A/T]AGGAAGAGAGGAGAA | 5521 |
rs528678400 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681056 | GACTGGTATTTAAAA[G/T]GCTTACATCAATGCA | 5521 |
rs528680532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931715 | AAAGGACTGAAATTG[C/T]CCAAAGTGAGGTTTG | 5521 |
rs528681246 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849154 | GTTCCTTTTATTAAA[G/T]AATGGTTTTAGAAAT | 5521 |
rs528692144 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804247 | GCACTAGGCATTGTT[A/C]TAGGCATTTTAAGAT | 5521 |
rs528701531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938948 | GCCACACCTGGCTAA[G/T]TTTTTGTATTTTAGT | 5521 |
rs528704558 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748705 | TGTTGATTGTATCAA[C/T]AGCTCATTCCTTTTT | 5521 |
rs528707825 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021872 | CTCTAAAAATGATAA[C/G]GATGATGGATGATAT | 5521 |
rs528713831 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797594 | TATATTTGTAACCTC[G/T]TGCTTAAAGAGACCT | 5521 |
rs528714171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654211 | GTTATCTCCTCCAGC[A/G]CCCTCAGTAACCAAC | 5521 |
rs528717864 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974720 | TTTGAGATGGAGTCT[G/T]GCTGTGTCACCCAGG | 5521 |
rs528724287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982110 | TTTTCTTCCTCCTTG[A/C]TTTGAGCTTATTTGC | 5521 |
rs528733611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836890 | TTGGAAGATTATGTT[C/G]CTCTGAAGTTCCTAA | 5521 |
rs528741123 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967447 | ATTGATATTATTCCT[A/C]TTTTATAAATGAGGA | 5521 |
rs528751683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741216 | GCAGTAAGGAAGGTT[C/T]TTGTCTAGCAGGCAA | 5521 |
rs528756672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629831 | CCTCTCCCTCTCCCT[C/T]GCCCTCTCGTCTTGC | 5521 |
rs528770841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146797579 | TATGATATAACAAGG[C/T]ATATTTGTAACCTCG | 5521 |
rs528776883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667666 | ATAGAACAGGGACTT[C/G]GCAAGCTGTTAGGAA | 5521 |
rs528781041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010473 | AACTAGATGGTCCCA[C/T]GTTGGGGGTGATGGG | 5521 |
rs528788152 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066481 | TGCTGGAATGCAAAC[A/C]TGGGTGAGACTTTCT | 5521 |
rs528792900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706496 | CAGCTTGATGTTCAT[C/T]AGCTTCTGGTAGGCA | 5521 |
rs528798973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836423 | TTTGTTTAAGGTGCT[A/G]AGTCAGATTAAGAGA | 5521 |
rs528803018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925974 | CAGCTACAGAATTTT[C/T]ACCTGGTATTTTTAA | 5521 |
rs528811192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841700 | AGAAAACCAAACACC[A/G]CATGTTCTCACTTAT | 5521 |
rs528816174 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146622675 | TCTGCTCCCTCTCCC[C/G]CTTCCACCACCCCTT | 5521 |
rs528822389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756643 | TTAGATATTTAAAAC[C/T]CTTTAACTTATCAGT | 5521 |
rs528838577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649280 | TGAGTTGTTCAGTGC[C/G]ATTCCTCATAAATCT | 5521 |
rs528843817 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048583 | AAGAAGAATATGATG[A/C]CCCATTCATTGAATA | 5521 |
rs528846008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954237 | TTCTCCAGGACCTCA[A/G]AATATATGAGGATAC | 5521 |
rs528846076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830630 | CCCGGGTTCAAACAT[C/T]CTTGGCTAATTTTTG | 5521 |
rs528847382 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001516 | ACACATCTGAACGTC[A/G]GAGGAACAAACTCTG | 5521 |
rs528853032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876159 | ATGCCAGAAATCTCA[C/T]TGCTATAAACTCATA | 5521 |
rs528859312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784257 | AAACAAAACAAAAAT[G/T]TAGTCACAACTAAAA | 5521 |
rs528870209 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019253 | TAACTGCTGTTCAAC[A/G]AAGTTACTCAAAACA | 5521 |
rs528873146 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146669109 | TTTAAAATCACTGTA[C/G]TTGAACATCAAATTA | 5521 |
rs528873519 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599847 | TGTTCCCCTTCCTGC[A/G]TCCATGTGAACACAC | 5521 |
rs528876397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687237 | ACTCTTGATTTTTAG[A/T]CCCAGTCCTGGAATA | 5521 |
rs528897340 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015194 | AATGTTCATCAGATG[A/C]ATGACTGAACCACTT | 5521 |
rs528904033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642976 | GCAGGAGGATTGATT[A/G]AGCCTGGGAGGTTGA | 5521 |
rs528904735 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951358 | CATGCCTTTTTTTTT[A/T]AAAAATTAAGTTCCA | 5521 |
rs528909222 | snp | C/T | 1.65847e-05 | 0.0028796 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600286 | GGGTGCCTGGGGTTC[C/T]ATACCTGGTAAGTCT | 5521 |
rs528911969 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637110 | TCCTGGGTGCATCTT[C/G]CCTCATTAGCCAAAT | 5521 |
rs528912189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593922 | GACCAGTTATAACCT[A/G]AGTGATAGATTCTGG | 5521 |
rs528912386 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022324 | GCACTTGTGGGAGGT[C/T]GAGGTGGGTGGATTA | 5521 |
rs528912445 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006856 | TACACTAACCATTCA[C/G]GGATAGTATGAGATG | 5521 |
rs528913808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617736 | GTCTCGCTCTGTCAC[C/T]GAGGCTGGAGTGCAG | 5521 |
rs528921546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606049 | TGAATTCAGTTATTC[A/T]AGAATTCAAAAATAA | 5521 |
rs528922806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146790542 | AATTACGCCAGCAAG[A/G]CAACAGAGATCAGTG | 5521 |
rs528927534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146875521 | GTTTAGAGTCCTTCA[C/T]ACTAACTACACAGCA | 5521 |
rs528933259 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989230 | AAGCTAAAGTGAACC[A/G]AATAGTTCCATATTC | 5521 |
rs528936095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729861 | GGCAGGGCCCTCATG[A/G]AGAACCTCTGCTAGG | 5521 |
rs528941275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146681776 | TGTCAACCTTCCCAC[A/G]TCTCTGAAATTCAGA | 5521 |
rs528941348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687547 | CCCTCCTCATTGGCT[A/G]TTCTGAAGATGAATC | 5521 |
rs528944643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146699804 | TTAACAATACATTTA[C/T]AAGAGTGTTGATTTG | 5521 |
rs528945882 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818179 | ACTATTTGATCAAAG[G/T]ACGTCTTTCCCGCCA | 5521 |
rs528954528 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811819 | TGATCTGCCCGCCTC[A/G]GCCACCCAAAGTGCT | 5521 |
rs528956250 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998056 | TCACAAGTGTGCAGA[A/G]GGCTCCAGGCAAGGC | 5521 |
rs528959663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995710 | GCAAGATAGTGAGCT[A/T]AAGAATACATAAGAG | 5521 |
rs528959797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648573 | GCAATAGTTCATACA[A/C]GGCCCTTGCTCTTGT | 5521 |
rs528964215 | snp | G/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606751 | AGACACATACTAGCT[G/T]GTTTCTGAACTATCC | 5521 |
rs528970004 | in-del | -/TAT | 0.0115144 | 0.0749975 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939995 | TGAATATTTACATAG[-/TAT]CTATCTACCTACACC | 5521 |
rs528981668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599560 | TGCCTCTATCTCCAG[A/G]CTCATCCTTCTGCCT | 5521 |
rs528983518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777125 | ATTCCACTCCTAGGC[A/T]TGCACCCCAAATAAT | 5521 |
rs528990027 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964719 | TTTAGTAGAGACAGG[C/G]TTTCACCGTGTTAGC | 5521 |
rs528996433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735577 | TTAAATTGGATGGGG[G/T]AAAAAAAGAGTCTCA | 5521 |
rs529001750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784691 | TACAATTTCTTTTTG[C/T]GTGGCTCTCAGCTCT | 5521 |
rs529009499 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692679 | GGTGGGACTACAGGC[A/C]CCCACCACCACGCCC | 5521 |
rs529019922 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922076 | AAAGCCTTTGCTAAA[C/T]TGTATGCTAAACTGT | 5521 |
rs529028058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913452 | AGTTCTATGCTTAGT[A/G]AAAATTGAAAGAAAT | 5521 |
rs529039011 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146723844 | CAAAAGCTCCTCCCC[C/T]TCTTGGAGGGCCAGG | 5521 |
rs529047473 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988973 | AAACTACTATGAACA[A/G]CTACACGTAAATAAA | 5521 |
rs529050423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146948093 | TGTGTTCATATAATC[A/G]TTTCCCTTACCCTAT | 5521 |
rs529051073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745936 | GCACTCCAGCCTGGG[C/T]GACAGAGAGAGACTT | 5521 |
rs529053616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996426 | TGGAAGAAAGTGTAA[A/G]GAAATAGAAGTGGAA | 5521 |
rs529061657 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038092 | TTCTTTGACCCATTA[A/G]CAAACCCACTTCCTG | 5521 |
rs529067374 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960905 | TGATTTATAAAACCA[A/G]TGTATGCCTATTGTA | 5521 |
rs529071646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939793 | GCTTTATATTTATGT[A/G]TAGCTTGCTTTTAAA | 5521 |
rs529074309 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991384 | AAGTTGATTTCATAG[A/G]AGTAGAGAGTAGAAT | 5521 |
rs529082122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862872 | TGGAAAAAAAAAAAA[A/C]AAAAACCCTGGCTTA | 5521 |
rs529084134 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928282 | GGTTTATATATATAT[A/T]TTTTTAGATCAGATC | 5521 |
rs529086776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818674 | TTTTCTACTTTACAG[A/G]TGAGAAATCTGAGAC | 5521 |
rs529092975 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714984 | GAAGGCTGCTAACTC[A/C]TATACACTTTAAAGT | 5521 |
rs529098165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030816 | CTGTTTTAAACTTTA[C/T]ATGACGTTATTATTT | 5521 |
rs529108726 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146676074 | CGGTGGAGGCCATGC[C/T]CTGACATGTATTGAA | 5521 |
rs529111469 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713866 | CATGTGAAATGTGAG[A/C]GGTTTATAAGTACAG | 5521 |
rs529118360 | in-del | -/AA | 0.0264011 | 0.111819 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680583 | GCGTTGCACACACTT[-/AA]AAAAAAAAAGTTCCC | 5521 |
rs529118687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850600 | CATCTTCCCATCTCC[C/T]CTTCAACAGAGCTAA | 5521 |
rs529120154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931102 | TATAGTTCTATACTC[C/T]ATACTTCTATAGTTG | 5521 |
rs529121682 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901227 | ACAAATAAATTCAAA[C/G/T]AGTGGCTCACTCCTG | 5521 |
rs529124360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770723 | TCACACAGGAGGTGT[C/T]GTCTGAGTTGGGACT | 5521 |
rs529126981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777702 | TTGTAATGGCACCAT[A/G]CTATGACATATACAA | 5521 |
rs529140644 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712195 | AAAATGGAAAGTATT[A/G]GAAACAAGCGTGCCA | 5521 |
rs529153243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074788 | TGAAATACACCTCAC[A/G]TCGACAGTCAAATTG | 5521 |
rs529153859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856796 | CGACCTGAAGTGGAC[G/T]GCCTACTCACTTGAG | 5521 |
rs529155877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983129 | AATGGGTTACTTGAA[A/C]ATTTTTTAGAATTCC | 5521 |
rs529165854 | snp | A/C/T | 0.00159649 | 0.0282165 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081800 | GTGGCCTATTTTGTT[A/C/T]CAAGGTTATTTTTGT | 5521 |
rs529173042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764174 | AGCCAGCCCCATGAC[A/G]GAAAGTGGAAGGGGC | 5521 |
rs529178858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850004 | CTTTGAAGGTGGAGG[A/G]TAAAGTACAAAGGGA | 5521 |
rs529180228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811936 | GACACACTGTTCATT[C/T]ATCACATCTCGATGC | 5521 |
rs529186123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895893 | ATGTGTACATAATTG[A/G]AAGACATCAAAATAT | 5521 |
rs529191987 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690129 | CCCTTCTTACTTTTG[G/T]TCTTTAGCAGAGCTG | 5521 |
rs529192029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989687 | CTCTAAGATCTAGAA[C/T]AACACAAGAATACCC | 5521 |
rs529208835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895262 | GATTAGTCATCTTTT[C/T]AAGAGGAAAGAATTC | 5521 |
rs529210586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682290 | ATGTAATACTACTTC[A/G]AACTTTTCAATATAT | 5521 |
rs529222003 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146940418 | TTTTTTGCTTTCATT[A/T]TGGATTGTGAGCCAT | 5521 |
rs529237750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933344 | TCTGTATCCAGGGAA[C/G]CCAATCCTCTGATTA | 5521 |
rs529241451 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031191 | GCAGTGAGCTGAGAT[A/C]ACGCCATGGCACTCC | 5521 |
rs529248112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758244 | ATGATTGCCCCAAAG[C/G]CTCAATCTGTAGCAG | 5521 |
rs529257600 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957621 | TTAGAGGGCAGTGGG[A/T]GCAGGTAGAGGCACC | 5521 |
rs529267739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656120 | AGTGAACTCTCTGTG[A/G]TACATAAGTTCTTGT | 5521 |
rs529269395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749878 | GTTGGGATTACAGGC[A/G]TGAGCCACTGCGCCT | 5521 |
rs529269419 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618784 | GGTGCTGTACACCCA[A/T]AAGCCGACACAGTTC | 5521 |
rs529273772 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061620 | TTTCTGATTGGCAGT[A/C]TGGACTGATGATTCA | 5521 |
rs529282152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976793 | TTATTTAAAATTTTC[C/T]TGGTGACTTTTGCAT | 5521 |
rs529300244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701333 | AATTTCCTAGATGCC[A/C]ACACTGCACAGTGGT | 5521 |
rs529307952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933701 | TCTTTTATTATTATA[C/T]TTTAAGTTTTAGGGT | 5521 |
rs529308885 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068125 | GGGTGGTAGAATGAT[C/G]AGTCATTTTTATTTT | 5521 |
rs529312927 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874990 | GATAAAACCATTGCA[A/G]TCTTTCCCAGAATAA | 5521 |
rs529322078 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632022 | GGCTTGTGTTCTTGA[A/T]GACTTTTATGTCTTT | 5521 |
rs529333425 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877488 | CAAAAGGAAAGAGGT[G/T]CGCCCGTCTGCAAAG | 5521 |
rs529336763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914405 | TACACAATTGTCCCA[C/G]TGCACTGCATCCTGG | 5521 |
rs529346127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969520 | CCTGATTGGATTTCT[A/T]ATCAGATCATTCCGC | 5521 |
rs529349615 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595517 | TCTGTAAATAATTCT[C/T]GAAAGATAGAAGTTG | 5521 |
rs529360031 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743136 | AATACACAAACCAGG[G/T]CCTATGGTAAGCACT | 5521 |
rs529369020 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061137 | CAGGCACTCTTCTAG[C/G]TGTTGAGGATACAGC | 5521 |
rs529374308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008688 | CCCCCACTCCTATGT[C/G]CCTGTGGTTGTTACA | 5521 |
rs529375080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922551 | ATGGGGCGGGGAGCT[C/T]AGGGTCTGGTGGCCA | 5521 |
rs529375227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707579 | GACACCTTGTAGGAC[A/T]TCTGCACCCTGATGG | 5521 |
rs529381513 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675586 | TATTAAGCATGCTCC[C/G]TGTTAAAGTCTGGGA | 5521 |
rs529389150 | in-del | -/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590394 | TTTTTGTTTTTTTTT[-/G]TGTGTTTTTTTTTTT | 5521 |
rs529389907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968977 | GGCTATGCTTAACAA[C/T]CAGTTCAAAACAATT | 5521 |
rs529403292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846847 | TTTAATGCTTATGAC[C/T]TTTTCTTAAACCTGC | 5521 |
rs529414736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779118 | AGTAGCTGGAAATGA[C/T]ATTTCAGCTCTGATT | 5521 |
rs529414823 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786152 | CATGTACCCCATAAA[A/T]ATGAACAATTACTAT | 5521 |
rs529418961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002987 | TCATTTTTTTCTGCA[C/G]TATGGCCTGGCCCCA | 5521 |
rs529423048 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030834 | GACGTTATTATTTCT[G/T]TTCATTTTTCTATCA | 5521 |
rs529441116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871362 | CCTAGATGGCCCAGC[A/G]GGACCATCTCAGCTC | 5521 |
rs529441920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708118 | CTCAGCACTTTGGGA[C/G]GCTGAGGCAGGTGGA | 5521 |
rs529448499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838286 | GTTACAGACTTAGAA[A/G]GAAGGAAGGGAGGCC | 5521 |
rs529452602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688883 | AGAAGTTCACGGTAT[A/G]AACTCTACGTGGCAC | 5521 |
rs529474461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743815 | GCCTCAAATATGGCC[A/G]CAAAATTATTGAGCA | 5521 |
rs529475698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785489 | GGAGGTGGAGGCTAC[A/G]GTGAGCTTTGATTGT | 5521 |
rs529475840 | snp | C/G | | | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617071 | TCCTGTCACTTGCAA[C/G]AACATGGATGGAACT | 5521 |
rs529476355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826107 | AGTCATCTCTAGGCT[A/C]ATCATCATTGCCACT | 5521 |
rs529479114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595402 | TCACCATTCACCTTC[A/G]GCATTTTGTCTTATT | 5521 |
rs529480660 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702057 | AGTGCAAATGAGTTA[-/A]AAAAAAAAAAAAAAA | 5521 |
rs529491100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877945 | CTGCCCAGGAAGCAC[A/G]GTGATCCGCAACTTG | 5521 |
rs529493173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146683709 | CTCATCCCCCAAAGG[C/T]GAAACATGTCAAAAC | 5521 |
rs529494448 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792569 | GACTATGGGAAAGCA[C/G]AATAGGTTAATGCAG | 5521 |
rs529498942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902660 | TTATTGACAGACTAA[C/T]TGTCCCCACACAAAG | 5521 |
rs529499812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601870 | TGCACTGATATCCAG[G/T]TTCTTATTATCTCTC | 5521 |
rs529502974 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870734 | CTGTTCATAAGGGCC[C/T]CTCTAGATTCCTAAA | 5521 |
rs529511175 | snp | C/G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648280 | CAAATGAAAGAGGCC[C/G/T]GAGTTTCTGAATTAC | 5521 |
rs529520486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736856 | CTCTAGTTGGTTCTT[C/T]TTAGAACCTATAACA | 5521 |
rs529524506 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656788 | GGCCGGATCACCACC[C/T]TCACTGTGCGGGTGA | 5521 |
rs529525097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832729 | TTTTACTATGCTTTT[C/T]CTATGTTGAGATACA | 5521 |
rs529542532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047569 | GCACTGGGTAATACA[C/G]TATATACTTGGTATG | 5521 |
rs529542821 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998909 | CCTTTTCAAAGGTAA[C/G]AGGAGTAGAAAGTGT | 5521 |
rs529549218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693816 | TTTATTAGAATTAGC[A/T]AATTGGGCAACTATT | 5521 |
rs529550980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997368 | CCATGGTATGAATGA[C/G]GGAATCCAACTGGGC | 5521 |
rs529569650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650881 | AACGAATCACACACT[C/G]TTCTTGTTCCATTCT | 5521 |
rs529576758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607791 | AGCTGAGCCTTAAAT[A/G]ATCAAGAAGCACTGG | 5521 |
rs529578417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820420 | TAAAGAATAAAAGCA[A/G]TTGGCATGGATTCTC | 5521 |
rs529583453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003640 | AAGAAAGGGACAAAT[C/T]CTCTACCAGTCAGCA | 5521 |
rs529586958 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949232 | ACATAATGGGAGAAA[A/G]TATTTGCAAACTATC | 5521 |
rs529586963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957562 | AGTTGATGGGATATA[A/G]ACAAATAAATACATC | 5521 |
rs529595111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731569 | GCTTGGGCTTTGAAG[G/T]CAGATGGATCTGAGG | 5521 |
rs529596254 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752662 | GTCCCCAGGTTTTTG[G/T]GGTGTGTGTGTGTAG | 5521 |
rs529602216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651408 | GTCACCTTACTGATA[C/T]ATAAATACTTCTCAG | 5521 |
rs529604994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864050 | CTAGAAACATAATTG[A/T]TCATACCATTTAATC | 5521 |
rs529610129 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786281 | TTTAGGATAACTCTA[A/G]ACACTGTCCCCCACC | 5521 |
rs529613136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677575 | ACAGGGTCTCACTCT[A/G]TCACTCAGGCTGGAG | 5521 |
rs529615606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688371 | GATGATAGAGTCCAG[C/T]GACCGCAGACCCCCT | 5521 |
rs529633149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146644401 | TGATGCGAATCCAAT[A/G]TATAGACAGCAAAAT | 5521 |
rs529647600 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589648 | CCTAGGAACAAAACA[C/T]TGGACCCACCAGAGA | 5521 |
rs529658247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731047 | AAACACAGATTAGAT[A/G]TATCTTCCTGCTGAA | 5521 |
rs529660238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737507 | ATATCTATGGAATCA[A/G]TGGAAGGTTACTTGT | 5521 |
rs529664267 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147083453 | AAAAACCCAAATCAT[A/G]GAAGTTACTGACTTG | 5521 |
rs529664673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941484 | GGAGGAGTCTTTGGG[A/G]CCCTTGAAAAATGAT | 5521 |
rs529668471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726427 | GCAGAAGGGGAGTAT[A/G]GCCAAGTATAAACAC | 5521 |
rs529677901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765743 | TTAATGCATATTTCA[C/T]ACCACAGGAAGTGAT | 5521 |
rs529686978 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864919 | AACGCCTACAGTAAT[C/T]ACAAAGGTATTCCTT | 5521 |
rs529691185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670996 | AGTGTAAGGTCAGTT[C/T]TCAGTTTAAAAAAAT | 5521 |
rs529706737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040110 | GCCTTTCTTCTTCCA[A/T]GCCATAAAATCAGGT | 5521 |
rs529721771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950250 | AATATATATACCTAC[A/T]TTTTACCTGTAAAAA | 5521 |
rs529724233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633414 | GCTGCCGTTTGAGGA[A/G]GATGGAGAAAATCAA | 5521 |
rs529730320 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731943 | CCTTTCTTTTTGACC[A/C]CAAAGTTAGAGCGTA | 5521 |
rs529732545 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884889 | GAAATGTCTTTCAAA[A/C]CTTTAAAAAATATAC | 5521 |
rs529732828 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841795 | TGGGGGTTGGGGAGC[A/T]AGGGGAGGGATAGCA | 5521 |
rs529740816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857654 | ACAACTGTCTTCTAA[C/T]GGTAATATCTTAAGA | 5521 |
rs529743130 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938129 | TCATGGATTCCAACA[A/C]ACTATTGATTATAGG | 5521 |
rs529746771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718030 | TATGTATATTATGTA[G/T]GTTTTTGAGTGTTTA | 5521 |
rs529747941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146684295 | ATCAAAGCATATACC[A/G]AAAATTAAAACCTGG | 5521 |
rs529757975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846144 | CAGCACTTTGGGAGG[C/G]TGAGGTGAGTGGACT | 5521 |
rs529758638 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884564 | AAAATATCTACTGTG[A/C/T]GTGATTTCACTGACA | 5521 |
rs529777915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033054 | GATTTTTTGAAAATT[A/G]TGAGACCATGCTATA | 5521 |
rs529782534 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942261 | ATTGTAAAACTAATA[C/T]AATTAGTGAAAAAGA | 5521 |
rs529789074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077543 | GGGTAGATTATGCCA[A/G]TTAAACCCCTTCACT | 5521 |
rs529789529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813882 | AGAGAGCAAGCAGGA[A/G]GAGTCCTGGCAAGAT | 5521 |
rs529797995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929646 | GAAAAAAATGGGCTT[A/T]ATTTTATTATTTAAA | 5521 |
rs529802668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984748 | TATCTTTGGCTTTTT[G/T]TTTTAATAAAAGTAA | 5521 |
rs529824370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885624 | ACTTCTATGTATATA[C/T]TGAAGAGAATTAAAA | 5521 |
rs529841402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717223 | GTACCAAGGCCATTT[C/T]CAGAAATGCTTTCTC | 5521 |
rs529842872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633081 | TGCTGCCATCAGCAC[C/T]CTATTGTTTCAGACA | 5521 |
rs529856087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019334 | TTAAAATAGAAAAGA[G/T]TCAGAATAAATTGTT | 5521 |
rs529858517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892286 | TCTCATAGTGGGTTT[A/G]CACACATGCCACACA | 5521 |
rs529860822 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146671129 | AATAACTTCCTCAAT[C/T]ATGTGATTCAATATT | 5521 |
rs529860960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929028 | AATATCCAAGTGACT[A/T]ATTCTCTCACTTCCT | 5521 |
rs529863315 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639579 | CTGAGGACCCAGCAA[C/T]ATCCTGCAAAGAACA | 5521 |
rs529871818 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033681 | CAAGTCAAGCCTTCA[-/T]CACAGGGATGCCACT | 5521 |
rs529888266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879034 | CCCAGAGCCCCTAGC[C/T]CCCTGCCTTTCTCCG | 5521 |
rs529891178 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834251 | AGTAAGTCCATGGAG[G/T]TAAGTACCATTATTA | 5521 |
rs529891427 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812121 | TAACTAGTTCTGTGA[C/T]GTGTGGAAGTTTCCA | 5521 |
rs529897787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620735 | TCCTTTCTCACGTCT[C/G]TCCCCCTGAGATAGC | 5521 |
rs529910898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063759 | CCCCAGGATTAGGCA[A/G]CATATTTCTTCTTGG | 5521 |
rs529912421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760550 | ACTGTATGTGATGAA[A/T]TATCAAACTAAACAA | 5521 |
rs529916752 | in-del | -/GAT | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781009 | CTCATCCACATTTCA[-/GAT]GATGATGATGATGAT | 5521 |
rs529921085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745484 | GAAAGACGAATGTTA[A/G]TTATTGTCATAGGGA | 5521 |
rs529924076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069209 | TAGCACAGTGAACTT[C/G]AGACCACAGACAGCA | 5521 |
rs529926632 | in-del | -/ATT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976150 | ATTATTATTATTATT[-/ATT]TCTGAGACACAGTCG | 5521 |
rs529930934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658001 | AAGGCCTTCAACAAA[C/T]ATTTATTGAGCATCT | 5521 |
rs529937722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794427 | CAGATAACTTTACCT[A/G]ATGATAGTTGCAATC | 5521 |
rs529940666 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886631 | GATAGATGTTCATGA[A/T]GTTCAAAAAATCATA | 5521 |
rs529942389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923559 | ATCCCTAGTGGGTTT[G/T]TCGGAAGCCCTTCTT | 5521 |
rs529945634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979083 | CCATTTCTACTTACT[A/C]TACTTCAGTAACATT | 5521 |
rs529956888 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964814 | ACAGGTGTGAGCCAC[C/T]GCACCTGACCGGCAT | 5521 |
rs529956924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648415 | ACCTTCAGAGCTTTA[A/C]TATAACTCTTAAAAT | 5521 |
rs529958129 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825431 | ACCTCAATAAAGTAT[C/G]TCTTTTTACTCTTTT | 5521 |
rs529961031 | snp | C/T | 1.66167e-05 | 0.00288237 | intron-variant, utr-variant-5-prime | PPP2R2B | GRCh38.p7 | 5:146856546 | TTCATGCTTCATTAT[C/T]GGGCCACTATTCTCT | 5521 |
rs529967538 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917052 | TAAGTGAAGGTTATA[A/C/G]CAATTATTACAAATA | 5521 |
rs529978172 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038641 | AGCCAACATATTTTG[G/T]ATACTTTCCCTATGC | 5521 |
rs529980579 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146852695 | CCCAATGACTGCTAA[C/T]GTGTTGGCCAGCAAC | 5521 |
rs529981092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620348 | TTTATTAGCCAAGCG[A/G]GACTGGTGCCTTTTT | 5521 |
rs529995979 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146794574 | CTAAATAGACAAGTA[C/T]AGAGCTTCTCAGAAA | 5521 |
rs529998491 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970610 | TCAAAAAACAAAAAA[-/AAG]AAGAAGAAGAAGGGA | 5521 |
rs530002583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879696 | CCAAATTTCAAACTC[C/T]ACTTTTGAAAGAAAA | 5521 |
rs530003154 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147062862 | CCTACCTATCAATGC[A/C]TCCAGAGATCCAATA | 5521 |
rs530014906 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988712 | CCTCAAGGAACTAGA[A/G]AAATAAGAACAATAT | 5521 |
rs530016597 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037104 | CCCAGGCAGTCTAAC[A/G]AGAGTTTAACCACTC | 5521 |
rs530022564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951154 | CATTATTTCTGAGAA[C/T]GGTACTCTGGAATCT | 5521 |
rs530030525 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049890 | TGTGGATGACACTTT[A/C]AAGGCATTTTTCTGA | 5521 |
rs530031822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597406 | GTATGTTGATTCTAT[C/G]AATTCTTAAAATTCA | 5521 |
rs530035929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971752 | CAACATATTAGGTTA[C/T]CAAACTTTTTATGTT | 5521 |
rs530040220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744614 | AGCACTGGGATATGA[A/G]CCAGGCAATCATTTG | 5521 |
rs530043256 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146640405 | AGCATCACATGCTGT[A/G]GAGCAAGAGCCTGTG | 5521 |
rs530047658 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739031 | AGTGCACCTATTTTT[G/T]TTTTAAGAGACAGGA | 5521 |
rs530049795 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991936 | AATATTATTAAAATA[G/T]TTATTCTTGCCAAAG | 5521 |
rs530053907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752890 | GACACATGGAGGTAT[C/G]AAAGTGTATTATCTG | 5521 |
rs530061455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597881 | AATTATCTTTGCATC[C/T]TACCATCTACAGCCA | 5521 |
rs530065983 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590684 | CAGGGTTCCTGGGCC[A/G]TCTGGCCTCTAAGGC | 5521 |
rs530067162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056248 | TAAAAGGAGCCACCC[A/G]TAATGCCATGGATCT | 5521 |
rs530067390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049095 | TTGAGAGAAAGGGAA[G/T]GAGCATGTGTGTGTG | 5521 |
rs530068410 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873179 | GAGTTGTCCTTGACA[C/T]CACCTTCTCCATCTG | 5521 |
rs530073919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788368 | GGAACAGTAACCTCC[A/G]AAGTAGGGAGGTTTA | 5521 |
rs530084210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910270 | TTTGCAGATAGAAAA[A/G]AATTTGAAGGCTATA | 5521 |
rs530084746 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781127 | ACATACATAATGCCA[A/C]CATGATATATATATA | 5521 |
rs530086957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998913 | TTCAAAGGTAACAGG[A/G]GTAGAAAGTGTCAGA | 5521 |
rs530088244 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838464 | TAATCCCAGTTACTT[C/T]GGAGGCTGAGGCAGG | 5521 |
rs530088272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690309 | GACCCTTCCCTTAAA[A/G]GATCGCTTTGAGAAA | 5521 |
rs530088918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004827 | CTCTTGTGGTCCTTA[C/T]TCAGACTCGTGGGAC | 5521 |
rs530096777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602756 | AAATTGCAAAAATTT[A/T]AAAAAAATCATTGAA | 5521 |
rs530098621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146609459 | AAAACTTAAATATGC[C/T]ACCAAAAAACTATTA | 5521 |
rs530101166 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623223 | ACGCGTCAGAACTTT[C/T]GGGTACACATAGGAT | 5521 |
rs530109382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146646999 | TAGGGCTGGGTGAGA[C/T]CTCTATCACTTGTTG | 5521 |
rs530115138 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990861 | CAATGATTCAATAGC[-/A]AAAAAAGAAAGAACA | 5521 |
rs530116776 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727063 | CACACTCTACAAAGG[G/T]GTTCTTTTGGAACTT | 5521 |
rs530135237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603342 | CTATTTTATAATGTT[C/T]AAATTGACAACAAAA | 5521 |
rs530152805 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958275 | TCTGGGTCCTTGGAG[C/T]CCTTTACTCTATTGA | 5521 |
rs530153315 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004478 | TCTCTTGTCCTGGAT[G/T]ACTGTCCTCAAGGTC | 5521 |
rs530160140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828420 | CATTGCTTTCAGAAT[A/G]TTCCTTATTTATAGA | 5521 |
rs530172087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904529 | GGGAGCGTGTTCCCC[A/G]AGTCCTAAAGTATAG | 5521 |
rs530176608 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762622 | TAATCCATTCTATTC[A/G]TCTCCATATATCCAG | 5521 |
rs530179467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732465 | TGATTTGGAATTTCC[A/C]CAGTGACTATGGCCT | 5521 |
rs530183692 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977403 | TATTATACTTTAAGT[C/T]CCGGGATACATGTGC | 5521 |
rs530192392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146719813 | GTTTCTATCATCTAA[A/G]AAGTATAAAGTTTCA | 5521 |
rs530193349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078234 | CAAATATCGAGTACT[C/T]ACAAAGTATTGAGCA | 5521 |
rs530196896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815034 | CCACGTGACTCAGAT[A/G]CGTTCCGCTGCTAAC | 5521 |
rs530199565 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652768 | AGGCAACACCCCCCC[C/G]CAAAAAGTTTTGCCA | 5521 |
rs530206148 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943821 | AAGACAATATCCCTT[C/T]GTATCTCTTTCCGTG | 5521 |
rs530206568 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768109 | AACAGGGTCTTACTC[C/T]GTCACCCAGGTTGGA | 5521 |
rs530215504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768090 | TTTTCTTTTTTTTTT[C/T]TGAAACAGGGTCTTA | 5521 |
rs530220855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781640 | GACAAAATTTTAGAC[A/G]AAAAGTATGTATTGC | 5521 |
rs530226613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999448 | AAAAAACAAAATATC[A/G]ATACTCAAGGCCTAT | 5521 |
rs530231444 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944766 | CCTTGGTAGTCCTCA[A/T]CCTTTAAAACAATTT | 5521 |
rs530241856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943822 | AGACAATATCCCTTC[A/G]TATCTCTTTCCGTGA | 5521 |
rs530244032 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735066 | AGGAGAGGTGGAATT[A/G]CTTTGAATTTCATTG | 5521 |
rs530244855 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146764623 | CTGCTGCACCTGCAA[C/G]AGTGAGTTCATTACT | 5521 |
rs530247979 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594834 | GAAGGAGATAGAACT[A/G]TGTGAAAGCAGAGGG | 5521 |
rs530249485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727585 | AGAATGTACTCTATT[C/T]AGATAGGTGCAGTAA | 5521 |
rs530256604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859855 | AGAACGTGGCCTATG[C/T]ATAGATTAGAACATC | 5521 |
rs530258338 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730866 | ATATCATTAAAAAGA[C/G]AGGTGATCAGGGAAG | 5521 |
rs530258694 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950473 | TCAAGTTGGCAGCAC[A/G]GTGAATCACCTGGAA | 5521 |
rs530259397 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739416 | ATGAGAGTCAGCCTG[A/G]CCAAAGGGCAAAGGA | 5521 |
rs530259832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146903985 | ATTGTCATCTTCTAA[A/G]CATGCTCCGGGGTTT | 5521 |
rs530261822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146821819 | ATGGATTTAACTTTC[A/T]GCTGGTTCAGTGTCA | 5521 |
rs530266566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665992 | ACTATCTGTGAAGCA[C/T]AATAAAGCGAAATGT | 5521 |
rs530284042 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732697 | ATGTAAAAAGCTTAG[A/G]AATATGCAAATCAAT | 5521 |
rs530295844 | snp | A/T | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917558 | TCAAAGTTATGCCCA[A/T]GGGCACACAATTAAT | 5521 |
rs530304781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860488 | ATGAGTGGATGGTAG[C/T]ATTCTCCTATGTTTC | 5521 |
rs530304957 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753917 | TGTAAACAGCAGTTA[A/C]GCTTCCCTGTCTCCT | 5521 |
rs530313685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027361 | ATTAGTGGGCCGGGC[A/G]CGGTGGTTCACACCT | 5521 |
rs530314477 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071633 | CAGATATTCACAAGA[C/T]GATATTTTTTTTTTG | 5521 |
rs530331286 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893129 | TATTCCCTCGTGATG[A/T]GTTTCTCTTCACTGA | 5521 |
rs530333144 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847310 | ATAATAGACTTACTT[C/T]CTCCTCTTGCCTACT | 5521 |
rs530333491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898598 | AACACCAAAAGCAAT[A/G]GCAACAAAAGCCAAA | 5521 |
rs530341662 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045057 | TGTCAAGACAATAAA[C/T]AGGTGTCCATGTTTA | 5521 |
rs530346520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986753 | AAAGGACAAAGAACA[C/T]TTATGAGCTATATAA | 5521 |
rs530350211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993099 | ATGTGTGCACCACCA[A/T]GCCCAGCTAATTTTT | 5521 |
rs530350879 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078570 | AGGCAGGCGGATCAC[A/G]AGGTCAGGAGTTCGA | 5521 |
rs530351330 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146986128 | CACATTGGAGAGGGG[A/T]GGAAGGACAGTCCCA | 5521 |
rs530354953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634786 | CACACACACACACCC[C/G]CTACTGGTTCTGTTT | 5521 |
rs530360008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775098 | ACTCTTTCAAAAAAA[C/T]GAAAACAAAAACACA | 5521 |
rs530362811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937162 | CAAAATTAGCTGGGC[A/G]TGGTGGCGCCTGCCT | 5521 |
rs530362953 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000480 | GTGGAAGTTGCTAAG[C/T]CTCTCTGGGCCTTTG | 5521 |
rs530377935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762001 | CACTACATTTCCAAT[C/T]TGTCTTGGGACCTAA | 5521 |
rs530386424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840927 | AGATATACATCTACC[C/T]TTAGGGAGGCTAAAC | 5521 |
rs530397082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795942 | ATTTTTATCTATGCA[A/C]ATTTTTATCTATGCT | 5521 |
rs530415100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809718 | TGCTACTAAGAACAA[C/T]GGGAAATGATTGGAG | 5521 |
rs530424185 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748146 | TTTTATGATCCCCAT[G/T]TAACCGATGAGTAAC | 5521 |
rs530426504 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886960 | TGGTCACATATAAAA[A/T]CATATATGTGACCAG | 5521 |
rs530429182 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678384 | ATTAGGTATTGATGG[A/G]ACGTATTTCAAAATA | 5521 |
rs530445429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146899244 | GTCCAAGAATGATAG[A/C]CTGGATTAAGAAAAT | 5521 |
rs530446254 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047682 | CAGGAAATAAAATGA[C/T]TTTCTGTGTATTAGG | 5521 |
rs530451458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892843 | AATCAGAATTTTTCA[C/T]ATTAATTTGTGCATA | 5521 |
rs530455242 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973155 | TATAAAAATGAGTAG[G/T]ATTTGATTCTTTTTC | 5521 |
rs530459988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930489 | CCCTGGAGGGATTGT[A/G]GCAATGGCCCAGTGG | 5521 |
rs530463408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072081 | TTCTGGTGTAGGATT[C/T]AAAACTTTGCTTTCT | 5521 |
rs530487004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011590 | CTCCTGCCTGATTGC[C/T]CTGGCCAGAACTTCC | 5521 |
rs530497212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874003 | ATTGTCCCTTCTACC[C/T]AAAATGCTTTCAGGT | 5521 |
rs530499996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887753 | AAATAGCCAGATGTC[A/C]CTGCCAAAAGGGCAC | 5521 |
rs530509728 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006281 | CAGCCAAATCTTAAA[A/C/G]TACTTACAGAATCAG | 5521 |
rs530513919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789153 | TCTGTAGGGTGGAAT[A/C]CGAGGGCAACAGCTG | 5521 |
rs530515457 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697838 | TGTGTGTGCCAGGCA[A/C]TCTGCTAAGCATCTT | 5521 |
rs530526285 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726203 | CACTGCATCCCCACC[C/T]CTCAGAGCCTGGAGC | 5521 |
rs530536436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975787 | TTGTATATTTTATTT[A/G]GCAAAATATCTATTC | 5521 |
rs530541486 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147020935 | CAGGTCTATTATGAT[A/T]TTCTATATGCTATAT | 5521 |
rs530551647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747301 | TGACAACTGGAAAGA[C/T]CCCAGTAGAGCAGCT | 5521 |
rs530559496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835654 | AAGCCAAGAAAGGTA[G/T]CCACAGTGCCTGGGC | 5521 |
rs530561124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795454 | AGACAATACTGCATG[A/G]TCTCACTTATATGGG | 5521 |
rs530572918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829074 | TAAAAAAACCTGCTT[A/G]ATGTGATTTAGAGTG | 5521 |
rs530585720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146959861 | CTAAGGAAGAACAAG[G/T]GAGACTAGAAGCAGA | 5521 |
rs530586657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146783460 | GCATCTGTCTGGACC[C/T]GTCATTTTCTCTTTA | 5521 |
rs530587065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919412 | CAAAATCTGGTTTCT[G/T]TTTCTCAACTATAGG | 5521 |
rs530587578 | in-del | -/ATAAT | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854300 | CAATTTTTAAAATAC[-/ATAAT]ATGTTACATATTTAT | 5521 |
rs530588778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000998 | CCAAAGAGTTAGTGA[A/G]AGATGAAGCTGGCTG | 5521 |
rs530589053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705181 | TGTTTTATCTTTCAT[C/T]TAAGAAACATTTGGT | 5521 |
rs530607786 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592469 | GTATTATGAAGCACT[C/G]TTCAAATCAAAGGCC | 5521 |
rs530626313 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869686 | AAGTGGGATGGGCAT[C/G]GGATGGAGGGTGATT | 5521 |
rs530626835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918659 | GCCCCTTTCTGGATG[A/G]GTCTGGTCTCATCTA | 5521 |
rs530640813 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687008 | GATCTGGAAAGTCAA[C/T]GTGTAAGTGTGTGTG | 5521 |
rs530653298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705923 | TTTCATTTCAGAATA[C/T]ATCTTTTCTCTTTTT | 5521 |
rs530666837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874371 | CTTGTTCTTCCTTTA[A/T]TATGTATAAACAAGA | 5521 |
rs530669749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842063 | CTAGCCACATCACTG[C/T]GAAGCCAAAACAACC | 5521 |
rs530670158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925137 | TACAGTGTTAAAATT[A/G]TTGTTTCACACAGTC | 5521 |
rs530680161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005560 | GCAAAAACCCAAGGA[A/G]GTGGCAGTCTTATAC | 5521 |
rs530681586 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807877 | CGATCTCAGCTCACT[G/T]CAACCTCCGCCTGGT | 5521 |
rs530709627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994679 | CCTATGACTCTCTGC[C/T]TCCAAGACCCGCTCT | 5521 |
rs530713726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599279 | CTTCTTGATTCCCTC[C/T]CCCTGCACATTTGAT | 5521 |
rs530718055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043535 | TGTGAGAAAATAAAC[C/T]ACTGTTGTTTAAGCC | 5521 |
rs530721366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994161 | CATTTCAACAACTCA[C/G]TGCAGCTCCAGCAGG | 5521 |
rs530724706 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957370 | GCCATGTAAACAAAT[G/T]ACTGCCATCCGATAT | 5521 |
rs530728807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861289 | TGTCGATCTCCTGAC[C/T]TCATGATCCGCCCAG | 5521 |
rs530736779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686452 | TGGCTTCAGATGATC[C/T]GGAGAGAAAAATAGA | 5521 |
rs530738019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642461 | CATGATATTAGAAAA[A/G]GATTGACAACTTAAA | 5521 |
rs530739849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741012 | ACCGCACTCTAGCCA[A/G]GCGACAGAGCAAGAC | 5521 |
rs530740491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829833 | ACAGGCCTAAAATTT[G/T]GATAATCTATTTTCA | 5521 |
rs530755034 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051456 | GTGTGACTCATAATA[A/T]CAACTTCATTTTTGG | 5521 |
rs530756366 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906442 | ATTCTCCTGCCTCAG[A/C]CTCCCTAGTAGCTGG | 5521 |
rs530762877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789760 | TTAAATAGGTGGTCA[G/T]GGCTGACCTCTCTGA | 5521 |
rs530771245 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867493 | GAGTAGAGAGGGAAT[C/G]TTTTGTATTTATTTA | 5521 |
rs530781789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147044656 | TTAAGCATCCTGTCA[C/T]CTGGGTTGTAGGACG | 5521 |
rs530783835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146698676 | GACAAAAGAGGCTCA[G/T]ATATTAAATGACTTT | 5521 |
rs530784298 | in-del | -/A | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146886827 | TTAAACTTTTTTAGT[-/A]AAAAAAAAAAAATAA | 5521 |
rs530786263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667756 | CCTGGTCTCTTAAAC[A/G]CCTTCTCTCTGCATG | 5521 |
rs530788156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604908 | AACCAGGATTCCTCA[A/C]ATTCTAGATATACCT | 5521 |
rs530788856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674799 | TGAACCAGTCTCCCC[A/C]AAAGTGTTATCCACT | 5521 |
rs530789337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906833 | TACAACACTGTATGC[C/G]CTTGTCAAAACATAT | 5521 |
rs530794357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762660 | CACAGAACTTGAAGT[A/G]CAGTCTGTGCTTAAC | 5521 |
rs530806475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147029781 | GGTCAGAGCAAGAAG[A/G]AAGCTGTCTGCAAGC | 5521 |
rs530808173 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146954995 | CATGATGAATAACTT[A/C]TCTGCTCGATGGTCC | 5521 |
rs530811111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146824227 | ATTCCAAAAGCCTAG[A/G]ACATAGAGTCAGTCT | 5521 |
rs530819343 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771280 | AGCACCAGCACAGAA[A/G]TTTCAAAGGCCATGT | 5521 |
rs530827777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146598624 | GGCAACTCTACTTTT[C/G]TAATTGCTCAGGACA | 5521 |
rs530830819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146900646 | TTTATTTTAAGCTCC[A/G]GGCTACAGGATGTGT | 5521 |
rs530834619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810494 | GCTACAATTCAAGAT[A/G]AGATTTGGGTAGGGA | 5521 |
rs530854485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769515 | AGATTTGCAAGCACT[A/G]TAAGGATCAGCAATC | 5521 |
rs530855623 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776932 | TAGGAAAATGCAAAA[A/T]ATACCACACTAAGAT | 5521 |
rs530855732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691866 | TCTGGAAAGTCCTTT[A/G]CCCTCTTTTTCGTAT | 5521 |
rs530874890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146912750 | CTGACCTTGTGATCC[A/G]CTCGCTTCGGCCTCC | 5521 |
rs530876527 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146843142 | CGGTGAGCCCAGATC[A/G]TGCCATTGCACTCCA | 5521 |
rs530885853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722892 | CTTTCTTTGACTTCT[C/G]TCTTGTCTACTGCCA | 5521 |
rs530901447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895147 | CTCCTTTCAACTCCC[C/T]GAAAGCTCCATGTAT | 5521 |
rs530916386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770273 | CAGGCGGAGGTTGCA[A/G]TAAGCCAAGATCACA | 5521 |
rs530917893 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146622860 | TCAGTATACCATTTT[G/T]TACTGGGGTCTATTA | 5521 |
rs530919761 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848828 | GCACAATTTATCTGG[A/T]GTTCTGCATGGGAGA | 5521 |
rs530928909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982197 | CTTCTTTCTAATCTA[C/T]ACATTTAGTGCTATA | 5521 |
rs530938581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146713926 | TTGGAGTTCAGGAGA[A/G]GGGATTGAGCTGGTG | 5521 |
rs530939578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894472 | TGAGACAAGGTCTTG[C/T]TCTCTCACCTAGGCT | 5521 |
rs530942805 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146932381 | GTCGTGGGAGGGTCC[C/T]AGTGGGAGGTAATTA | 5521 |
rs530948501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146722025 | AACCATAAGGTAGAT[A/G]TCATTATTACTACCC | 5521 |
rs530950284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729499 | CAAGACCATGGGGAA[A/C]ATGTCTCCAGGCCAT | 5521 |
rs530960186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146862118 | GAAATCTCAGATCAC[A/T]TCTTTTGACATCTCC | 5521 |
rs530967404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015270 | TCATTGCCCTGTTTT[A/G]AAATTCTCATTGAAT | 5521 |
rs530969971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668221 | TTCTTCAACCTGTCA[C/T]TATTTTGACAACCCT | 5521 |
rs530983144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756722 | GGTTTCCATGAGAAT[G/T]AAATGAGTGAATTCA | 5521 |
rs530992826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146982643 | GTTGTCGAAGTCTCC[A/C]ACTATAATTATAGAT | 5521 |
rs530993710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836986 | TGGTTTTAGGTGCTA[C/T]GCCAACAACTAGCAG | 5521 |
rs530996254 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658161 | AAGATGAGAGCGGAA[C/G]TCCTGGGTGTCCACC | 5521 |
rs530998917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146635941 | ATGTATGACGAATGC[C/T]AACCTTTAATATCAC | 5521 |
rs531000463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700563 | AAGCTTTACTCAGAC[A/G]CTAGTTTGTGGCCTT | 5521 |
rs531002629 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693721 | TCCTCATGGGGCTCT[A/G]ATGAGGATTAAATAA | 5521 |
rs531009796 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897847 | AATATGGCAAATTTA[G/T]TTTTAAATTATTAGA | 5521 |
rs531012338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882114 | AACCCTGTCTCTACT[A/G]AAAATACAAAAAATT | 5521 |
rs531019206 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928013 | CCAAAGTGCTGGGAT[C/T]ACAGGCCTGAGCCAC | 5521 |
rs531019459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066678 | GCACCGTATTAGACA[A/G]ATAAGAAAGATATGG | 5521 |
rs531028141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146849349 | TGTCTCTAACTTTAA[C/T]TCATTACCACATGTA | 5521 |
rs531028966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014790 | CCTAATGCTAGATGA[C/T]GAGTTAGTGGGTGCA | 5521 |
rs531029182 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788106 | TGCCTCCTCCATGCC[A/G]TTGTGTGAGCATTTG | 5521 |
rs531030818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146974986 | GAACCACCGTGCCCC[A/G]CCTATTTTTTAAATT | 5521 |
rs531031146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022779 | TCGCATCATAAACAG[A/G]GCAAACCATAAGATA | 5521 |
rs531048609 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073093 | GGTTTTGTCCATGAC[C/T]GGCCTCATCGTCCAG | 5521 |
rs531048863 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607168 | ACTATACAGAAGACA[C/T]ATCCAATAATTTTGC | 5521 |
rs531052602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629859 | TGCTCTGTTGCCTAG[G/T]CTAGAGTGCAGTGGC | 5521 |
rs531062574 | snp | A/G | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082219 | TTTTATTGAATTCCT[A/G]TACGGAAACCTTCAT | 5521 |
rs531064040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831354 | ATACAAAAATTAGCC[A/G]AGTGTGGTGGCAGGT | 5521 |
rs531064631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939556 | ATGTTTTTTCTAAAA[A/G]ACAAACTTTTTGGTG | 5521 |
rs531071801 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745072 | TCAAAGCTGGGCACT[A/G]TGGCAATAGAAGAAA | 5521 |
rs531079369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654962 | CTTGTCTGAGCCATG[C/T]TGGCAGAGTAATTGA | 5521 |
rs531085315 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000657 | CAAAAGTAATTGTGG[-/T]ATTTGCCATTTTTAA | 5521 |
rs531090807 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995261 | TAAGATTAAATAGGA[A/G]CAGTGCCTGCCTTTT | 5521 |
rs531096945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882840 | GAAAGACTGACCTAT[A/T]TCAGGCTTGTGCTTT | 5521 |
rs531106021 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146842252 | TCCAAAATTATATGG[C/T]CTGCTGTACATTTAC | 5521 |
rs531137824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700019 | TGAATTTATATGGAA[A/C]CCCGAGGGATTACGA | 5521 |
rs531145104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742061 | ATGGGCTCTGGAGGA[A/G]TCAAACCTTCACGTT | 5521 |
rs531153249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007367 | CTAAAGGTTTGTAAA[C/T]GCACCAATCAGCACT | 5521 |
rs531162607 | in-del | -/A | 0.499273 | 0.0190544 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022559 | GCAAGGCTCCATCCA[-/A]AAAAAAAAATCCAAA | 5521 |
rs531168751 | snp | G/T | | | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147081889 | TTTCTACAAATATAT[G/T]TAGCCAATACTAATG | 5521 |
rs531169986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146594700 | AGGGAACTGAGCCCC[A/G]GTATCAGGCTCTGGA | 5521 |
rs531172437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967465 | TTATAAATGAGGACA[C/T]TGAGGGACAGAGAAG | 5521 |
rs531180816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146623585 | TCAATGACAATTTCA[C/T]TGCATTACAGACATT | 5521 |
rs531184442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907500 | ACAGAAGGGCAAAGT[C/T]TACAACAGCATCTCT | 5521 |
rs531185765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914246 | ACATTTTCTTTTCCC[A/G]TTAAAGAAGACCTTC | 5521 |
rs531186360 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688238 | ATAGCAAATATAACA[A/T]GTCCCTCCAAAATAT | 5521 |
rs531188979 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022903 | AACATAAAGAACTTT[C/T]CAAAAAAGAAAAAAA | 5521 |
rs531190700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785304 | GTAACCCAAGCACTC[C/T]AGGAGGCCGAGGCAG | 5521 |
rs531193987 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791913 | CCGCCACATGAGAGT[G/T]AGGCCCTAATTGGCC | 5521 |
rs531195960 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060059 | AAAATTAGCTTATTT[A/G]ATATTAATCAGGATG | 5521 |
rs531197230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146947445 | TTCCTGTTTTTTCTG[A/G]AACTGTTGGAGAAGT | 5521 |
rs531197908 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968414 | ACATCAAAGTGGGTT[A/G]GATACAGTGGGGTGC | 5521 |
rs531199309 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045995 | GCATAATAAAGCCTC[A/G/T]TTAGATCTTGTCCTA | 5521 |
rs531204273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706960 | GAGGAAGTTGATATC[A/G]TCAGCCCTTCCAGGC | 5521 |
rs531206192 | snp | A/G/T | | | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607198 | CCCAGTGAGAGAAAC[A/G/T]GCCAACAATTTTCCC | 5521 |
rs531223622 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146825104 | AATGCAACTCCGCTG[A/G]TATTTTAAATTTACG | 5521 |
rs531224320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831891 | CCATGCATCTTATTG[C/T]CTTTGAAGGCCTTCC | 5521 |
rs531225832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661196 | GGCATCCGTGTGCAG[A/G]AGCTAGGGAGGTAGC | 5521 |
rs531239425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045447 | ATACCATATAGCCTG[A/G]GTATGTAGTAGGCTC | 5521 |
rs531244135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791100 | GTCACCTATCTTTTA[A/G]GACCTGTTTCTCTTC | 5521 |
rs531247048 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682841 | TTCTAAATCAAATCA[C/G]TCTCTTAGTGTAAAG | 5521 |
rs531250239 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617807 | TCAAGCGATTCTTGT[A/G]CCTCAGCCTCCCCAG | 5521 |
rs531250991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619411 | CTTGAACCTGGTAGG[C/T]GGAGATTGCACTCCA | 5521 |
rs531253601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595306 | GGGGGCACAGCAGTA[A/G]AGGTATATAAACTGG | 5521 |
rs531264245 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749626 | TTTTTTTTTTTTTTT[C/T]CGAGATGGAGTCTCA | 5521 |
rs531264962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038193 | CACTATCAGAGGGAA[A/C]TGGGGATGGCTCATT | 5521 |
rs531281073 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964726 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 5521 |
rs531292229 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146730918 | TGACCAGGAAATGTA[A/G]CCAAAAGATATTCTC | 5521 |
rs531293984 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146870515 | ATGCTGGCACCTTGA[G/T]CGTGGACTTCCAGAC | 5521 |
rs531300462 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782671 | TTTTTTCCTTGCCCA[-/T]TTTTTTTTTAAAGAG | 5521 |
rs531306615 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995820 | AGGCACACAGGAGAG[A/C]AAGATTTCCCCTCCC | 5521 |
rs531313275 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146682391 | TAACATAAACTAAGC[A/G]TCTATTGATGGCAAG | 5521 |
rs531328300 | snp | A/G | 0.000148381 | 0.00861212 | synonymous-codon, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146600366 | GTCCCTGGTCATGAT[A/G]TACCTCCCACTGTGG | 5521 |
rs531328537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146955750 | CTTGATAGGTTGTCA[A/T]TAACAATAGTCTTCT | 5521 |
rs531331028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025431 | GAGGCAAGCATTACC[C/T]CAACGCTAAAGTCAC | 5521 |
rs531332788 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639549 | GATCAGGACACAGAG[A/G]GGCCGAGGTACTGTC | 5521 |
rs531338188 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146748394 | TATAGGACTATATCA[C/T]AGCCAGGATCTGACA | 5521 |
rs531341041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146962454 | ACGAGGTCAGGAGTT[C/T]GAGACTAGCCTGACC | 5521 |
rs531352887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818840 | CTTGGGTAACCTTGA[A/G]CCATTACTTTAACCT | 5521 |
rs531363905 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074805 | CGACAGTCAAATTGA[C/T]GTTTTTCTCTCATTA | 5521 |
rs531364961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812860 | TATAAAACCATCAGA[C/T]TGTGTGAGACTTACT | 5521 |
rs531373638 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751519 | AGCATATCATGACTC[A/G]AGGCCTTTGCATTTT | 5521 |
rs531376982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146718434 | TTATTAATATTTGTA[A/G]CCTGATCATTTGGAT | 5521 |
rs531380923 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784728 | GGATGACTGCCGTGT[G/T]GATTTTAAAACATTG | 5521 |
rs531391966 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624643 | ATAATCAATCATCCT[C/G/T]TTTACACCAAGCCCT | 5521 |
rs531392184 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779315 | ACTGTCCACATCTTG[C/T]TTCCAGAAAACGGAT | 5521 |
rs531392882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146901973 | GCCATAATTCACGGG[A/G]CCTGTAGGCTATTGT | 5521 |
rs531397445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882104 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 5521 |
rs531405465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933804 | GTCATCTAGCATTAG[A/G]TGTATCTCCCAATGC | 5521 |
rs531409844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717011 | ACATGACATAAATGG[C/T]TCACAACTGGAGATT | 5521 |
rs531412042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031261 | ATCTTTATTTTGCTT[G/T]TATCTTAAGGGTTAT | 5521 |
rs531412409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146949112 | GGTGATACATGTGCT[A/G]GGTACTTACAGATGA | 5521 |
rs531415894 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146685611 | CATTCAGGAGTCAGA[C/G]CTGGTAAAACTGAAT | 5521 |
rs531424282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146902435 | TAATAATATTGCTAC[C/T]ACCCACAACAATTAT | 5521 |
rs531429352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997049 | ACTCAAACACGGGAT[A/T]GCACCCAACTCTAAA | 5521 |
rs531429377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989704 | ACACAAGAATACCCA[C/T]GTTTACCACTTTATT | 5521 |
rs531439841 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983422 | CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC | 5521 |
rs531441512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146996492 | GCACCACACTGAGAA[A/G]ACGGGATTGTTACCC | 5521 |
rs531453512 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771425 | GCTGTCAGTCATTTT[A/C]AGATCAACTACAAGT | 5521 |
rs531462624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146759262 | TCTTAGAAATGACCT[C/T]TCAGGGAATTTTCCT | 5521 |
rs531467800 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146995127 | CATCTTCATCTGGGC[A/G]TCTAATAACATTCTT | 5521 |
rs531473478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643601 | AGGGGGAAAGGGTGG[G/T]AAGGAGGTGAGGGAT | 5521 |
rs531477109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907876 | ATTTCCATAGTATGC[A/T]GTGGTTTGTTAGTCT | 5521 |
rs531489545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068898 | CATGGACAAACGACT[A/G]TGCCATAATTTTGGG | 5521 |
rs531496494 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806595 | TGGCCATCATCATAT[C/G]CAGCCTGGAGCTTTC | 5521 |
rs531505640 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146851194 | CAGAGATCTGTTTAT[A/C/T]AAGTAATTTTTCTTT | 5521 |
rs531505969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844858 | ACTTTCACTTATTGC[A/G]TTTTTACCTTTAGCC | 5521 |
rs531523185 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879932 | CTCCACAAGTTTAGC[C/T]AGATGGGCCCAGAGG | 5521 |
rs531523338 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147075654 | TTTCAGGTTTCCCAG[C/T]GTTAGTAACGGTGTC | 5521 |
rs531526428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765527 | ACCCTTTGTGTTAGC[A/C]TCTGACTTATTATTG | 5521 |
rs531526724 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146632064 | GGGCTGAGTTGTGCC[A/C]CCCCCCCCGCCCATT | 5521 |
rs531527547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031870 | GAAACTGGATTCTCA[A/T]CTCTCACCTTATTCA | 5521 |
rs531529772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147023560 | GATGTAAACAATAAT[C/T]ATAAGAGGGATATCT | 5521 |
rs531534136 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781960 | TAGGATCATGGGGGC[A/G]GTTTCTGTTGAATGG | 5521 |
rs531549180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895966 | TGAAAATCGCAAAAC[A/G]AACTGTCCAAAGGGG | 5521 |
rs531550963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038704 | ATCATCAAATGATTT[C/T]TGTGCAATAGGATTA | 5521 |
rs531557511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146656894 | TGTCTCTGCTCACCC[A/G]CTTTGAGTCTTCCTC | 5521 |
rs531558950 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662728 | GGTTTATGTTAATTT[A/T]AAAAATTCTGATTAT | 5521 |
rs531560972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856930 | ACCTATTCTAAGCTT[C/G]AGGGGGTGGAGCCTG | 5521 |
rs531561268 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855632 | AAAGGGAGCTCTTCT[C/T]TTCTGAATGTTGTAC | 5521 |
rs531565140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008740 | GCACACCTCAGATGT[C/T]TGAGGGTTTCTATTC | 5521 |
rs531573109 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146884923 | GAAATACCACTTTAC[A/C]GAATTTATTCTAAGA | 5521 |
rs531576091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146970448 | TCTACTAAAAAAAAT[C/T]AGCCATGCGTGGTGG | 5521 |
rs531578130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146963361 | CTCTTCTTAGCACCA[C/T]CACGGAGTAGGGATC | 5521 |
rs531580800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772147 | TTTAAAAAGGTTCTA[C/T]ATGGGCTATCATGGA | 5521 |
rs531588598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977439 | ATGAAGGTTTATTAC[A/G]TAGGTATACACGTGC | 5521 |
rs531606527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608374 | TAGAACCTGGGCTTC[A/C]TCATCTCCAGGTTGG | 5521 |
rs531612163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146651480 | TTCTTTCTGGTGGAT[C/T]AGAGAATCGGCAACT | 5521 |
rs531637612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799350 | GGGAGCTCTATTTAC[A/T]TTTGGTTAAATGCCA | 5521 |
rs531643060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069341 | TATAAGGAAGATTAC[A/G]TTACTGAAAATTCTC | 5521 |
rs531646771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146625195 | TTGTAAAAATATTGC[A/C]ACTTTTAAAATCTTA | 5521 |
rs531650196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146977965 | CACTGTCTTCTACAA[C/T]GTTTGAACTAATTTA | 5521 |
rs531653781 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983749 | AACAGAAAAAAGAAA[A/T]TCTGTTGTATTTACC | 5521 |
rs531653787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146758347 | ATCTGGGGCAAGAAC[A/C]CTCATTCTTTGAATT | 5521 |
rs531658028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061309 | GAGTGACTGCTTTGC[C/T]TGATGGTCAGGGAAG | 5521 |
rs531664297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890286 | GGGCCAGGGAAGTGC[C/T]GCAGGAGGAGCTGTA | 5521 |
rs531667571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024215 | TATCACCTACTGGTT[C/T]TGTTTCTCTGGAGAA | 5521 |
rs531668545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146934256 | CCTGAGGAATCGCCA[C/T]ACTGACTTCCACAAT | 5521 |
rs531673913 | snp | A/G | | | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617355 | CATTTAAAAATAAAG[A/G]AGTATAACCAGATCG | 5521 |
rs531678099 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146708985 | TACTAAAGACAGAAG[A/T]AGTAAATACACAGTT | 5521 |
rs531685207 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988521 | CATGAAAAACTAATG[A/G]GTCAATGAAGAAAGT | 5521 |
rs531687872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878872 | GAGGCTGCGGCTGCT[C/G]TTTGCTGCAGTGGGG | 5521 |
rs531694787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147018323 | ATGACATAGCCACCA[G/T]GAAAGGCAGTATTTT | 5521 |
rs531695576 | snp | C/T | 3.3089e-05 | 0.00406736 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | PPP2R2B | GRCh38.p7 | 5:146878053 | TGTTGATTTTGCGGG[C/T]ATCAATGTCCTCCTC | 5521 |
rs531707446 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792943 | GTGACATGATCTGAC[C/T]TAATTTTTTATAGGA | 5521 |
rs531710776 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707840 | TCTCTCTCTATAGAC[-/A]AAAGTTTATCAGAGA | 5521 |
rs531715925 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658148 | CTAGAAAAGACAAAG[-/T]ATGAGAGCGGAAGTC | 5521 |
rs531719958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054700 | TTTCAGAACAGGCTG[A/G]TCGCCAGCTCAGTTC | 5521 |
rs531724596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743876 | GTGGGTGGTTTACAG[C/T]CAGGGTTACCAAGAT | 5521 |
rs531729758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694511 | ATTGCTATACAGAGA[A/T]ACAGAGAAATCATGG | 5521 |
rs531729805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786840 | GAAAGCAATAAAAAG[G/T]TGAGGCCTGTAAAAT | 5521 |
rs531742231 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956381 | CTATGTGGAACTGTC[A/C]TCACAGAAAAATAAT | 5521 |
rs531746336 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147052139 | TTTGTATCTTCTTAT[C/T]TCAAGTTAAAGAACA | 5521 |
rs531752936 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839299 | GCTGAAGTAGGCAGA[A/T]CACCTGAGGTCAGGA | 5521 |
rs531753172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146864957 | CCATTTTAGAAGGTA[A/G]TTTAGTCCTATCATC | 5521 |
rs531756538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928358 | TCTAAAGGACACCTC[C/T]AAGTCACCATACCCA | 5521 |
rs531759092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147024980 | GAGCCAGAATAAAAA[A/G]TGGAACCACGAATAG | 5521 |
rs531759878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147003060 | TATAAATTACTATAC[A/G]ATCCTGCAGGTTGAC | 5521 |
rs531763832 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643485 | TCTATATGTCCTAGA[C/T]TGAATAGAAGGAAGG | 5521 |
rs531774566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601953 | ATGTTATTGGAGCCC[A/G]TCACAAACTGCCTCT | 5521 |
rs531781403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004215 | AAAAGACTGTCCAAT[G/T]AGAAACAAGCCACCC | 5521 |
rs531782504 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146999111 | TTTATTTGGCTGTGC[A/G]TTCATTGTTTGAGCA | 5521 |
rs531783863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618838 | GCAAAGGCAGAGCAA[A/G]CCAAACTCCTCAGAG | 5521 |
rs531793716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780184 | CAAACAAACAAAAAG[A/C]CTCAATTATCTCTGG | 5521 |
rs531799210 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645531 | AGACCCCACAGTTCC[C/G]CTGGAAGCCTGCCTG | 5521 |
rs531803191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055308 | CAGAGAGCTCGGACA[A/G]ATGTATGTGGCAGCA | 5521 |
rs531804533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915863 | CAATTTCAACACTGT[C/T]ACAACATCTTTGTCT | 5521 |
rs531808199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701502 | CCACGGCCTTTACAC[C/G]AAGAATCTTCCCCAC | 5521 |
rs531819575 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001901 | CTGTACTTCTGGGCT[G/T]AGCCAAGGGTCAACA | 5521 |
rs531819665 | in-del | -/GTT | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971639 | TCAAGTGATAATTCA[-/GTT]GTTATTTTGAAGATA | 5521 |
rs531824632 | in-del | -/AAG | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589495 | GGTTTTTCACAAAAC[-/AAG]AAGAAGAATTTGTCT | 5521 |
rs531825508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677622 | CGGCTCACTGCACCA[A/G]GCTCAAGTAGTTCTC | 5521 |
rs531834375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871869 | TTCTCTGTACCTTGA[A/C]ATTTCTTATTTTAAA | 5521 |
rs531842662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774410 | GGTTCTTGGATCCAG[A/G]TTTTAGTAAAAATCA | 5521 |
rs531843233 | snp | A/T | 0.000882062 | 0.0209822 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147055625 | AGACACCAGCCCACT[A/T]TTCCCACCCACCCAG | 5521 |
rs531843743 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923086 | GCTCCAAAGCTTTGA[C/G]AGCTCCAGGTTTTTC | 5521 |
rs531844069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061922 | CTCTTAATTTATAAA[C/G]AGAAGTCAGAGCAGG | 5521 |
rs531857457 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786821 | GAGAAAGATGAAGTT[G/T]CCTGAAAGCAATAAA | 5521 |
rs531860694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645155 | TTGTGTGAACACAGC[A/G]TATTTGTTTGATGAG | 5521 |
rs531862542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652046 | CTGTAGAAGGGTCAG[C/G]GGTCCTCTGAATACT | 5521 |
rs531872406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702197 | CCCCTGAGTAATTCT[A/G]ATCTCAAATCTTACT | 5521 |
rs531876025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832867 | CAGTAGGCTATACCA[C/T]CCCAGGTTTGTGTAA | 5521 |
rs531877750 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009283 | GCATTTTAATGCTGA[A/T]CCCATTCCTGGCTTC | 5521 |
rs531882439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146991610 | AGAAATGAAAAATGT[C/T]TAAAGTAATGGATAT | 5521 |
rs531900470 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146596408 | CACTGGACCTCACAA[C/T]CTATTAACTAATTTC | 5521 |
rs531902989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773956 | TAAACATTCCCACTG[C/T]AACCCGTCGTAATAG | 5521 |
rs531917671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804110 | AGGTGGAGGTTGCAG[C/T]GAGCAGAGATCATGC | 5521 |
rs531922914 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950296 | TCAGGGAACTTTGAA[C/T]ATGATAGATAATTTA | 5521 |
rs531931122 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146619881 | TCCTTTCTTCCTTAC[C/T]GGTTAATTTGGCCAC | 5521 |
rs531936114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147040187 | AGCCTCAAACTCTAA[A/T]CAGTTTGGTGAGGTC | 5521 |
rs531937585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957718 | ATAGTTTTGTACATT[A/T]GTTGCAATAACGTTC | 5521 |
rs531938202 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048871 | ATATGTGGGAGAAAC[A/T]GTTCTGCCTACTGGA | 5521 |
rs531943619 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731626 | AGCTGCAAAACCTTG[A/G]GAGAGTCAGTCACCC | 5521 |
rs531946483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792533 | CAATAAATAAGTAAG[G/T]TATGTAGTATGTTAG | 5521 |
rs531953610 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726634 | CCTAACATCCTAAAA[C/T]CAGTTAGTAGTGGAG | 5521 |
rs531958722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827306 | ACTTTCAAAGTACCA[C/T]TGGGAGATTTGTGTT | 5521 |
rs531969881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808542 | GGAAAGGAAGAACTG[A/G]CCAATCCTGAATAGC | 5521 |
rs531976912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147047665 | ATGATAAAATTAAAG[A/G]CCAGGAAATAAAATG | 5521 |
rs531982859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688936 | AAGATTGCCATGTCT[C/T]GAGGGGCAAAAGACA | 5521 |
rs531986899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766624 | ATGAGGTGATTTCTA[C/T]TATTTATACTTTCAA | 5521 |
rs532005258 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845624 | CTGAAGAACAGACAC[-/T]GTGCGTGGTCAGCTC | 5521 |
rs532015927 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146814012 | CCTCTCACTTGAAGA[A/G]TATCAGTAAGGCAGT | 5521 |
rs532019971 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731856 | AACTTTTTTTTTGTC[C/T]TTCCTCTATGAGAAG | 5521 |
rs532043604 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942908 | GTTCACACCATTCTA[C/T]TGCCTCAGTCTCCCG | 5521 |
rs532046557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858981 | AAAATGTTAGTGGTC[A/G]GTGTCTTACAGAGAG | 5521 |
rs532047930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146665293 | AGCCACCGCCACCCA[A/T]GATCTTAGCTAGATC | 5521 |
rs532053706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858234 | ATCTCCAGAGTCTGT[G/T]TTCTTGACTACTTTT | 5521 |
rs532058546 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666341 | TTAGTTACCCTGAGA[C/T]ATGGAACCGTAAATA | 5521 |
rs532069860 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980037 | GAGATATCCACAAAA[C/T]TGAATTTAATTTTTA | 5521 |
rs532072705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639068 | TTTCAGGGGTGGAAA[C/T]GGATGCTCCATGTGC | 5521 |
rs532072931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802108 | CCACACAAACACCCA[A/G]TGGTTCTTGGAGCTT | 5521 |
rs532077447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146753033 | CTTCAAATTTTTCAT[A/G]GAGCTTCTTGTGGAA | 5521 |
rs532077739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633485 | CCAGCTGGCAGGAGC[C/T]GGGGCTCGTAGCCGC | 5521 |
rs532090816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146820932 | AAATCTCCTTTTCCA[C/T]GCCATGCCCTCTGCA | 5521 |
rs532095623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146935753 | TGTCTTCAGTGTAAA[G/T]TTTGGAAAAGGGTAG | 5521 |
rs532104175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147077723 | GTGTTTGTGACCAAC[C/T]TAATTCTTCTTTTTA | 5521 |
rs532105798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146892335 | AGAAATGTAAAATAG[C/T]GTTGAAATAATAATT | 5521 |
rs532106794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664755 | AGAGGAACTATTTTT[C/T]GGTAGCGATAGCCTT | 5521 |
rs532111624 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146729058 | AAAGGAAAATGTGGG[A/G]AAGTTTGGAACTTCC | 5521 |
rs532126442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147026173 | ATAAAGAATTGTCCA[A/T]GAATGTTCATAGCAA | 5521 |
rs532126451 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760121 | CACAGCATGTAACAC[A/T]CAGTAAACACGAATA | 5521 |
rs532136852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627165 | TGTGTGTCTGTGTGT[A/G]TGTTTGCAATCCTGC | 5521 |
rs532139456 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070028 | ACTCCTGACCTCGTG[A/G]TCTGCCTGCCTCGGC | 5521 |
rs532139589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027063 | TAAAAGAATAAAAAA[A/T]TTTTGGTATATTCAC | 5521 |
rs532144234 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795279 | CAATAGATAAGATAT[A/T]GAAACAACTTAAGTG | 5521 |
rs532148837 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146692717 | TTTTTTGTATTTCTA[G/T]TAGAGACGGGGTTTC | 5521 |
rs532152875 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147033152 | GACCTAAAAGCTGCT[A/G]TACTATAACAGTAGA | 5521 |
rs532155792 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694351 | GGGCCATATTTATAT[A/G]GTCACGTGATTAGCT | 5521 |
rs532159407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943074 | AGTGCTGGGATTACA[G/T]GCGTGAACTACTACG | 5521 |
rs532162761 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689988 | ACTGCTGAATAAGCA[G/T]ATGTATCAATAAATG | 5521 |
rs532164508 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648713 | GAGTTAATGGGAAAG[A/T]GTACCTCTGGGGCCT | 5521 |
rs532167789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726911 | TAAATGTTAGATTTG[C/T]ATGGCTTTGTAACTA | 5521 |
rs532170345 | in-del | -/A | 0.0475351 | 0.146656 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082542 | AAAGTGTTTCATACT[-/A]AAAAAAAAAAAGAAG | 5521 |
rs532170694 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146811719 | GCGCCCACCACCACG[A/C]CCGGCTAATTTTTTT | 5521 |
rs532172384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880272 | TTCTATTTTATTTTC[A/G]TCTAGTGCTTAAGAC | 5521 |
rs532181645 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146911138 | CCCCAAGTTGGAGTG[C/T]AGTAGTGTGATCTCA | 5521 |
rs532195252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147019880 | AGAGCTATGGGAATA[C/T]ACCGCTCAGATCTCG | 5521 |
rs532202540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603443 | AAGCCAGTGCAGCAA[C/T]ACTGTAAAGCCTCAC | 5521 |
rs532207077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146597498 | AGCATATATATTCAA[A/C]AAGCTTGCCTTTCTT | 5521 |
rs532208926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923583 | CCTTCTTGGGTTTCA[C/T]AAATACTAAACATTT | 5521 |
rs532210778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146802710 | AGGTTGGTAAACAGT[C/T]TTTCCTCAGCTTGGA | 5521 |
rs532225453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885785 | CAATAGAATATTATT[C/T]AGCTGCAGAAAGGAA | 5521 |
rs532231915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071037 | GACTGTGGCAAAGGG[A/G]ACATCAAAAGAAATT | 5521 |
rs532236892 | in-del | -/AA | 0.0158469 | 0.0875917 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652983 | GGCATTGCGATGGAT[-/AA]AAAAGTGACTTTGCC | 5521 |
rs532238950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146918434 | GCTTGCATTTATTGA[A/G]AGGTAAATAGGTACT | 5521 |
rs532254354 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846719 | TTCTTTATTTTTTTT[A/T]AAAGTAGCTACTAAA | 5521 |
rs532256070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979119 | CCTTGCTATTTCTCT[A/G]ATAGGACATATACGC | 5521 |
rs532264840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070330 | AAAGTTATTTATACA[C/T]TCTTTTTTAAAGCTC | 5521 |
rs532266924 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853192 | TAATGTGTTGAGGCC[A/T]TAGAATTAGAGGCAT | 5521 |
rs532272170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929743 | AAGCAGCAGTTTTGC[A/G]TGTGGGCTCTGGAGA | 5521 |
rs532274174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146709893 | ATGCTACTATACATG[C/T]CTTTCCATCTTTGTT | 5521 |
rs532275722 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917889 | GTTTAACAGTAAAGT[G/T]CCAAGCAATCTGACA | 5521 |
rs532276741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056956 | AGGAAATGATTTAAA[C/T]GTCCATAAAAGAAAA | 5521 |
rs532285150 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146658667 | TCTTCTCAGGAGTAC[C/G]CACAGCCTAGGTTCT | 5521 |
rs532288774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005391 | GAGCTTTAGAACTGG[A/G]AAAGGGAAAAAGAAT | 5521 |
rs532302409 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971806 | ACATCTTTAACATAC[-/T]TTTTTTATTTTGGAA | 5521 |
rs532307053 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652925 | ATTTTTAAAGTGAAG[A/T]TCATACACTTTTGGA | 5521 |
rs532308309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787819 | GTGATCCACCCACCT[C/T]GGACTCCCAAAGTGC | 5521 |
rs532312677 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606723 | TCTGGGTTTTCTGTC[G/T]GGGCTGCGACACAGA | 5521 |
rs532317979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147011358 | CTTAACTTTTGTCTG[C/T]AAAAATTATCACCCT | 5521 |
rs532325476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840654 | CTCAGATACTGCCCC[A/T]TTCAAATAGTTCTAT | 5521 |
rs532325587 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146965584 | AACTCTGCTGCTATA[A/T]GCCTGCCCTGTCCTG | 5521 |
rs532328437 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072103 | TTGCTTTCTGGTCTC[C/T]ATAAGACATTGGACA | 5521 |
rs532340018 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146765634 | TTTCTTAACATCTAC[C/T]ACACTGGCTCAAATA | 5521 |
rs532346374 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834895 | GTTTTCTGTTCCTGC[A/T]TTAGTTGGCTTAGGA | 5521 |
rs532351000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745594 | TCTCTTTGAACTTCA[G/T]TTTCCCCACATAAAC | 5521 |
rs532354787 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042973 | TGGCTGGAGTGAGGT[A/G]AGTGAAGAGGAGTTA | 5521 |
rs532368755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147042318 | CCGTCTCTTGGCTGC[C/T]GGCTAAACAAGCGGA | 5521 |
rs532370323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803262 | ATTTTGTATTTCTCA[C/G]TGCTGCCTGAAACCC | 5521 |
rs532371625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146604035 | AGTAAAAAGTATTTC[A/G]ATACGTGCCAGGCCC | 5521 |
rs532376016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147000345 | AAGGGCTCTTCAAGT[C/T]TGAACTTCTTTAAAC | 5521 |
rs532376675 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768232 | GTGCATGCCACCATA[A/C]CCAGCTAATTTTTTT | 5521 |
rs532376772 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146822465 | TCCACATTCATTACT[A/G]CTCCAGGGCCTTTGC | 5521 |
rs532378330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146678521 | CACTCCTATTCAACA[C/T]AGTGTTGGAAGTTCT | 5521 |
rs532394624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952201 | TCTTGCCCTGTTGAT[A/T]TTTTAAATCCTTTTT | 5521 |
rs532396477 | in-del | -/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147007767 | AAGAGCTGTAACACT[-/G]ACTGCGAGGGTCTGC | 5521 |
rs532400756 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146629332 | AAGCACCAAACCTAC[A/G]AGTTATCTTAGATTC | 5521 |
rs532404149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146958856 | ATTTAAACCTCACAA[C/T]AAACTTATGCAATAG | 5521 |
rs532405615 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004721 | TCAACCCTGAAGTCT[A/T]GGCATTGGAAGAAAC | 5521 |
rs532419469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592147 | TGTCCTATACCAACT[G/T]GTCAGTGTGACTTGG | 5521 |
rs532424285 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074657 | CTGAAAAATCATTCT[C/T]ATAATCTCGAATTTC | 5521 |
rs532426270 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025774 | AAATATTTGAACAGA[C/T]ATTTCACCAAAGAAG | 5521 |
rs532426276 | in-del | -/T | 0.0206 | 0.0993762 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980657 | GATTAATCTCTCTTG[-/T]TTTTTTATGTATTCT | 5521 |
rs532427838 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829472 | TGCAACATGAGTAAA[A/G]TCACATTGTTCTTCT | 5521 |
rs532443935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056344 | ATTTTTTAAAATACT[A/G]AAGCCCAAACAATAG | 5521 |
rs532445272 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593379 | GATCACCATTCATGC[A/G]GTCTTTTATTCAACA | 5521 |
rs532451703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816410 | CTCCAAAAACAACAA[C/T]ACTGAAACATTTTGG | 5521 |
rs532461209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147064529 | CCTGGGCTGTGATAA[C/T]GGACACATTAATTGC | 5521 |
rs532467030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704785 | CTAGACTGGTAATTT[C/T]ATACATAAAGTATTA | 5521 |
rs532467063 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799192 | GCAAATCTTGTTTTC[C/T]AGCGATGAACATATT | 5521 |
rs532495713 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146944816 | TGTGATGAAAAAAGG[A/G]CATCTAGATAATAGG | 5521 |
rs532498331 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859929 | AAAAGAAATTCTATC[G/T]GAAGTTTACCTTGGA | 5521 |
rs532502790 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147050563 | TCTAATCCTAGCCCT[G/T]GCATTTAACAGCTGT | 5521 |
rs532509332 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146867326 | AGAAAAATATTACAA[C/T]CCCTAATCAGCAGAT | 5521 |
rs532512179 | in-del | -/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735962 | TGGTGACTGATTTAG[-/T]TTGGCTGTGTCCCCA | 5521 |
rs532512287 | snp | A/G | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770304 | CCACTGCACTCCAGA[A/G]TGGGTGACAGAGTGA | 5521 |
rs532514134 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815727 | ATCCCCACTTTTCCA[A/C]ACACACACACTTTAG | 5521 |
rs532521336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782085 | CCAGCGATTTGAATA[C/T]TGGCTCCCCCTTTGC | 5521 |
rs532522357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938052 | TCCCAGAAGCTTGTG[C/G]GTGGAAAGGAAAAAT | 5521 |
rs532522858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860584 | TGCCCCATATGCAGA[C/T]CTCTCCAGTAGGTCC | 5521 |
rs532523451 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869305 | AGATAATAAAATCAG[A/G]AAGGAGGACATTTAA | 5521 |
rs532534968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775193 | GACAACACAAGCAAA[C/G]AAAACTATAAACTAA | 5521 |
rs532538528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146641205 | GGTCCATTTTACAGC[C/T]GAGGGAACTCAGATA | 5521 |
rs532545912 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978009 | AGTGTAAAAGCATTC[C/G]TATTTCTCCACATTC | 5521 |
rs532546860 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727672 | CGTAAGTCAAAAAGA[A/G]ATTTTAAAAAAATTA | 5521 |
rs532556245 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803726 | GACCAAGTTAGGCAT[C/G]CCTGGGTTAAAGCCT | 5521 |
rs532556483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147079382 | ATATATAATATGTGA[C/T]ATAAAATGGGATATA | 5521 |
rs532560945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621849 | TTTTGCTTAATGACT[C/T]GGTCATGGGGAAGGA | 5521 |
rs532576139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680549 | TTAAAGTATAATAAT[A/G]ATAATAAAAAAAACC | 5521 |
rs532584107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633981 | TTGTTTCTGTTCTCT[A/G]ACTAATGCATCTTCT | 5521 |
rs532587382 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146762109 | AAACATAATGGAATG[A/T]TATGATTTCATACAA | 5521 |
rs532590593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672710 | ACCTCCCTCCCTCTA[G/T]AAGTAGTATATGCAG | 5521 |
rs532596502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, missense | PPP2R2B | GRCh38.p7 | 5:147035176 | TGACTCACAGTTCTG[A/C]ATGGCTGGGGAGGTC | 5521 |
rs532598778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146873749 | CTGAGTAGCTGGGAT[C/T]ACAGGCATACACCAC | 5521 |
rs532604946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146768798 | GAGATTTGCTGTCGC[A/T]TCTGCCTAGTGTTTC | 5521 |
rs532608676 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146950889 | AGATATATAAGAAAT[A/G]TTTAATTCTTAGTGC | 5521 |
rs532613243 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146704124 | AATACTTTACTGCCC[A/C]ATCCATCTCTGCATA | 5521 |
rs532628672 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146647072 | CCAAATGCCAGTCAC[A/T]GGAAGTCATGACTGT | 5521 |
rs532635455 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628363 | AGGAGGGGATTTCTG[C/T]GGCCAATCCTTGGGC | 5521 |
rs532645278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921845 | CAACAAGTACTACTA[C/T]TATTAATTATTTAGA | 5521 |
rs532648615 | snp | A/G | | | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917841 | TTACTGAGTCCTGTT[A/G]TTTTATTTGCTACTC | 5521 |
rs532651219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146993806 | AGAAATATCCAGCAC[A/G]GTTTTTTTTTTTAAA | 5521 |
rs532655631 | in-del | -/AAAGATCTCAGGAATGTTTG | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853047 | TGATTAACAGAGATT[-/AAAGATCTCAGGAATGTTTG]AGAACTTTCTAACAT | 5521 |
rs532659812 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146953760 | AGTAGTTATTATTCC[G/T]ATTTAACTGTTAAAA | 5521 |
rs532670985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925271 | GGATTTGTGCTATCA[C/T]AGAGTACCATTTCCG | 5521 |
rs532681306 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895475 | TTCCCAGTGCCTAAG[A/T]ACTGACACACAAAAG | 5521 |
rs532685622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147072151 | AGCTGCCTTAATCTC[C/T]TCATATCTATGAAGA | 5521 |
rs532696343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810355 | GTGAAAGGAGTTTCC[C/T]GTTATAAAACCATCA | 5521 |
rs532706134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146712403 | AGAATGAATAAACTA[A/G]TGTTGATTTTCATCA | 5521 |
rs532717845 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981310 | TTCTTAGTCCTCACA[A/C]CTAGAAGTTTCTATT | 5521 |
rs532724244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146754882 | GCTTCCAAATGACTG[C/T]AGTCCTGGCTTAGAC | 5521 |
rs532724278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147021790 | TAACAATATTCAGCA[C/T]CATATAAAAATTTCT | 5521 |
rs532726808 | snp | G/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866780 | CATTGCAAGCACTCA[G/T]TATATAGTGGCTCTT | 5521 |
rs532732296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146931647 | TGAAGTCACTTTTAG[A/C]TTCTTATTAGCAGGT | 5521 |
rs532738326 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146854712 | CACCTTGTACCTCAC[A/T]CTGATCGCTAAGCTG | 5521 |
rs532744624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027987 | TCACGGACTTTGTGG[A/C]TTTTGTCTGTACTTC | 5521 |
rs532747859 | in-del | -/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808519 | CACTAAGAGGTAAGA[-/G]GCTGTCTGGAAAGGA | 5521 |
rs532755294 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146675718 | TCGTTCCTCTGGGCA[C/T]GGGGCTCAGTTTTCT | 5521 |
rs532756778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787282 | GATCACTATTGGCCA[A/G]CTCCAGCTAACTGTG | 5521 |
rs532769892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146747991 | CCAGGGCTGAACCTG[C/T]CTCTGGATTCTCTAT | 5521 |
rs532776947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146980770 | GGAATGTTTTATACA[C/T]GCATAGGAGAATTGC | 5521 |
rs532779367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667625 | AAAATATTACAGATC[A/C]TCGAGACTGAAATGG | 5521 |
rs532805546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756095 | GATGATGGGAAGGAA[C/T]AAACCAGAGGCATTT | 5521 |
rs532808363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147066371 | TAATTTAATCCTCAC[A/C]AGAGCCCTGGATGTA | 5521 |
rs532811502 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725465 | CTGGAAGCTAGGATA[C/T]GCATGCATGCATCTA | 5521 |
rs532827177 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146782142 | AGGCCTCCCCAGGAG[C/G]TGAGGAGATGCTAGC | 5521 |
rs532842409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741928 | TGTTTCTATGCCTTT[A/G]GGTAAGAAATTATAT | 5521 |
rs532844031 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616553 | ATCTAATCCATTTAA[A/G]AAAATGAGCAAGTGA | 5521 |
rs532852562 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697937 | AAGTATATAGTTTGG[A/C]CGACTGTATCTCTGA | 5521 |
rs532858025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146673345 | ATCTTAATTTGCAAA[C/T]GTTAACTGGGTTAAT | 5521 |
rs532864261 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146756218 | ATAAGAATAACTAAC[A/G]TTTATAGGGCATTTT | 5521 |
rs532864713 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146734621 | CCATATTCCAGACAC[A/C/T]CCACCCCCTGGCCAT | 5521 |
rs532864740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001489 | AAACCCACCAGAAGG[A/G]AGAAACTCTGGACAC | 5521 |
rs532870036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628903 | CACTGTCTTCTCTCA[A/G]CTTACATGTGTTGGT | 5521 |
rs532885124 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943357 | ACAGAAAAATGCATA[C/G]TCAAAAAGTAATCAG | 5521 |
rs532887089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887173 | ATAATCAATAAAGAA[C/T]TACTAATGACATATC | 5521 |
rs532889029 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078398 | AGATTTAAGTGCAGA[A/G]TAAGAGAATAATGGA | 5521 |
rs532892463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605170 | AATCAGTCAACTCAG[A/G]TACAACTCACAGCTA | 5521 |
rs532897084 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147081210 | AGACCAACAAGAAAA[G/T]AAATATATAGCAGAA | 5521 |
rs532902104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146741102 | CAGATTCTTTAGGAA[A/T]GGGGATCTAGGCATC | 5521 |
rs532903047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146654194 | CCACCCAACTCCAAG[G/T]TGTTATCTCCTCCAG | 5521 |
rs532909351 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882073 | ATGAGGTCAGGAGAT[A/C/T]GAGGCCATCCTGGCT | 5521 |
rs532910314 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147014590 | TGTCCTTTGCAGGGA[C/T]ATGGATGAAATTGGA | 5521 |
rs532912230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914042 | CTATGTATATATGAA[A/G]TCACAACAACTATAA | 5521 |
rs532912626 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810593 | GTGAATCGTCCAGCC[A/G]GGATTTGAACGCTTG | 5521 |
rs532921833 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051994 | ACCACTTTTGTAGAT[A/G]AATCCTCCCCTACCA | 5521 |
rs532931158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789826 | AGAGGCCAGACATAA[G/T]AATGTCTGTGGATAA | 5521 |
rs532938057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605937 | ATGTACAGATATGAA[G/T]AGATCTCCATGGAGC | 5521 |
rs532943819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919459 | GCAACCTATAGCTAC[A/T]GCTGTTAGTCCTTCC | 5521 |
rs532946009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146691948 | TTATGTAATACCTAC[C/T]TAAAAATGCTGTCCT | 5521 |
rs532948727 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773916 | TCTCTTCTCCCAAAT[A/G]CCTCATCCTTGTTTC | 5521 |
rs532951876 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147081139 | AGTGTCCCAATTCCT[A/G]AAAACAACACAAGGA | 5521 |
rs532959903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147022208 | GAACATACTGCAATT[A/G]GAGTTCTAGAAAGAG | 5521 |
rs532971341 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904127 | CATCACTCTCTCTCT[C/G]ACTCCTATAGAACCA | 5521 |
rs532976853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146946354 | CAACAGCAAGAGCTC[A/C]CATGCCAAGTGATGC | 5521 |
rs532978002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146599361 | GCTACCATCACCAGA[C/G]CAAATTGCCATCATC | 5521 |
rs532984201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146975142 | GCAAACTGAAACTCT[A/G]TACTCACTAAACAAC | 5521 |
rs532993660 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146987950 | CAAGCAAGTGGAAAC[A/C]AAAGAGGGCAGGAGT | 5521 |
rs532993954 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146957767 | TATCTTGAATAAATG[A/G]TCTCAGTTTCTAAGT | 5521 |
rs532995385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146728993 | GTGGAAGCAACTTTG[A/G]AACTGGGTAACAGGC | 5521 |
rs533001053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830610 | GCTCACTGCAATCCC[C/T]GACTCCCGGGTTCAA | 5521 |
rs533004485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146906891 | TTTTTGAAATGTCAA[C/T]TGCACTTTATGCAGC | 5521 |
rs533005242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146869128 | AGTACTGGGCACATA[C/T]GAATAGGTAGATCAG | 5521 |
rs533011487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771178 | CAGAATTCTAGAAGC[A/G]GGCCTAATCCCATGG | 5521 |
rs533027980 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146776484 | GCCCTACCCAAATAT[A/G]AACAAGAAATTAACT | 5521 |
rs533035325 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006119 | GAGGAACTCCCTTCA[G/T]GATAGGACGATGGAT | 5521 |
rs533049849 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146716315 | ATGAGATCCATGACA[C/T]TGTCACTTACATGTG | 5521 |
rs533053814 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146894565 | CCACCTCAGCCTCCT[C/G]AGTAGCTGGGACCAC | 5521 |
rs533055908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988889 | TAAAGACAAAACTCA[A/G]ATAAATAAAAACAGA | 5521 |
rs533056386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146810965 | ACCTATGAGTGAGAA[C/T]ATGCGGTGTTTGGTT | 5521 |
rs533059235 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146988217 | ACAAATCATCTAGAC[A/C]AAAAATCAACAAAGA | 5521 |
rs533073393 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146770414 | TAAAAAATTATTGCA[A/T]TTAAAAAGAATCCTT | 5521 |
rs533092664 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836728 | CAAAGTTCAGAGAGA[G/T]AGCTACAGACACAGA | 5521 |
rs533096946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146855582 | TATGATAAAATATTT[A/G]TCTAGAGCCTTTTTC | 5521 |
rs533098521 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920104 | GCACATAATCAGGCC[A/G/T]TACATGAAGGTTATA | 5521 |
rs533100400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147006747 | CCTCACTGCTGAGAA[A/G]AGAGGACTCTGCACC | 5521 |
rs533100850 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887065 | CATTAAAAAGTGAGG[-/A]AAAAAAGATGAAATT | 5521 |
rs533103514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146642924 | TAGCCAGGTGTGGTG[G/T]CATGCACCTGTAGTT | 5521 |
rs533118448 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146593883 | TTGCAATGGATCCTA[A/C]GGGTGCAAAGGCAAA | 5521 |
rs533121156 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636105 | CCTTCTAACTTTCCT[A/C]CCTTTATTCACATGA | 5521 |
rs533122132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147001976 | TGACCCTGCGGCCAT[A/G]AGCGGAACTCTCAAA | 5521 |
rs533127809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661232 | TCATTTTGATGAACA[A/G]GGTAGCTCCTCCTGA | 5521 |
rs533133452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147073874 | AACCCCATCTTTACT[A/G]AAAATACAAAAAGTA | 5521 |
rs533140036 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589558 | TTTTCAATCAAATGG[A/T]ATTGCTTAATTAAAA | 5521 |
rs533147726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146763992 | TTGGCCTCCCAAAGT[A/G]CTGGGATTACAGGTG | 5521 |
rs533155836 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146777576 | TGAATGTAATTAACG[C/T]CACTAAATATGCACT | 5521 |
rs533156489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147045203 | TTATCTCTGTTTTGT[A/G]TGTCCCACCCCTTAA | 5521 |
rs533161802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146636815 | TTCCCCTTTCCCCCA[A/G]GCCTGACACTTTTTA | 5521 |
rs533166125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146735343 | CCCCCCACAATCCTT[C/T]TACTCTCTTCTCCCA | 5521 |
rs533176753 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030732 | ACTACTTCCCCGAAA[A/G]TCTAAGAGAGCTTAA | 5521 |
rs533189502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146661814 | ATATCACTATTTCTC[A/G]AAGTGTGTTTCCCTG | 5521 |
rs533195795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146674961 | GGTGGTATTATATTA[C/T]TATTATTGTTATTAT | 5521 |
rs533201777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784198 | TTTCTGTAAATAGCA[C/T]GCATGATATGCAGAA | 5521 |
rs533216857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146686809 | AGTGTGATTTCTCAC[C/T]ACCCAACTTCCATTT | 5521 |
rs533220858 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146660087 | TTTGCAAATAGCTCC[A/G]TCCTCATTGTCATGA | 5521 |
rs533221492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147037322 | TGATGCAAGAAAAAC[A/G]TAGCTACATGTGAGT | 5521 |
rs533222648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146967934 | GAAAATTTTCCCTTC[A/G]AGGTCTGGACATTTC | 5521 |
rs533231170 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146677816 | TACAGGCGTGTACCA[C/T]CACTCCTGGCCCGCT | 5521 |
rs533233884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664332 | CACAGCTTTATTAAT[A/G]TTGACGTGATATTCT | 5521 |
rs533247109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818551 | CCAACATTCACCCCA[C/T]TGTTCCGAGGGAACT | 5521 |
rs533248966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798198 | ATTGGCCCTTTCCTT[G/T]TCTACTTTATCCCAA | 5521 |
rs533254979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146668336 | TGGTCACTATTCCCT[A/C]GCTAGAAATTTTATT | 5521 |
rs533259353 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850549 | CTACTGCTACTACCA[C/T]AAAGCCCTTGTACAT | 5521 |
rs533260620 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146882942 | ACATTCGTTTTTTTA[A/T]CCACCCTTGTCATGG | 5521 |
rs533271116 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146637333 | ACATTTTTGGTTATA[C/T]AACTGGGCTTGGGTT | 5521 |
rs533274439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983392 | TCACCATGTTAGCCA[A/G]GATGGTCTTGATCTC | 5521 |
rs533278268 | snp | A/T | 0.0418186 | 0.138422 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976108 | TCATTTTTTAAAAAA[A/T]TTATTATTATTATTA | 5521 |
rs533280476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889649 | ATGCATCTCTTTCTT[C/T]GGTTTATTTTAATCT | 5521 |
rs533280641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015362 | AACCTTCTACTGACA[C/T]TTGAATTTTCTTCAT | 5521 |
rs533283290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687158 | ACCTGGAATAATAAT[G/T]GCACTAATTATTAAG | 5521 |
rs533294596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631272 | CTTCAAGTTATAGAA[G/T]TAAAACAACAACCTT | 5521 |
rs533295340 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939124 | GGCTCCTGAATCTTT[A/C]CTGTCTCATCAATGA | 5521 |
rs533301928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707161 | TGGCCCAGAGTCTCC[A/C]GCTGCCGCCTAAGGC | 5521 |
rs533304275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926963 | TGACAACTTTGCTTG[C/G]TGTCTGCACTGCCCA | 5521 |
rs533305435 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907354 | TCAAGCAGCTCTTCT[A/C]CCAGAGCTTCTTCAG | 5521 |
rs533307699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146942480 | ATGATGCTGTGATGT[A/G]TCTTTCTTCTTTCAC | 5521 |
rs533307715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818126 | TGACTCCATTACAGA[C/G]GAGCCATCCTGCTAG | 5521 |
rs533307731 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745853 | GTCCCAGCTACTTGG[C/G]AGGCTGAGGCAGGAG | 5521 |
rs533317273 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805884 | AATTATCGGCAGCTC[A/G]ATGAGTCTGACTTCC | 5521 |
rs533323052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792035 | TGTTTCCTAAGGATT[C/T]AAGGAGATGTGGAAC | 5521 |
rs533328196 | in-del | -/A | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615503 | AACTTAGAGTATAAT[-/A]AAAAAAAAAATTAAA | 5521 |
rs533329208 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061120 | TAGCAGCTATTAAAT[A/G]CCAGGCACTCTTCTA | 5521 |
rs533338674 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784900 | TACGTAAGTTAGATA[A/C]CAATTTACAAAGGAA | 5521 |
rs533341321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146687709 | GCTTCTCATGGGCTC[C/T]TTTGGTAATGAGATT | 5521 |
rs533358756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617854 | CGTGTGCCACCACGC[C/T]CAGCTAATTTTTGTA | 5521 |
rs533362505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707543 | TAGGAGCAGCTGCAG[A/G]AGGCCCGGGTGCCAG | 5521 |
rs533366086 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146750367 | AGCAATCACATTAAA[C/G]CTATATATCAATTTG | 5521 |
rs533367119 | in-del | -/TA | 0.00716266 | 0.059414 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146755852 | ATCCTCGTCTGTGGC[-/TA]GACTGGCTGCAGGCA | 5521 |
rs533383860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791172 | GGAGTAGAATGGTGC[A/G]GGTCTTTTTGAAAAG | 5521 |
rs533392619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146601163 | CATTGTATGAATATA[A/C]CACATTTTGTTTATC | 5521 |
rs533394562 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799065 | CTCTGATTCCCATTC[C/T]GGGGCAGCCAGAACA | 5521 |
rs533399183 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146826336 | CTTCTAGGTATAGGT[A/T]AAATTAGGAGCTGGC | 5521 |
rs533408747 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146907951 | AGGAAAAACCATGTT[G/T]TTCTTCCTTATTAAT | 5521 |
rs533408805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914961 | CATTTTCATAAAGAT[A/G]TTCTGGTTAAAATGC | 5521 |
rs533408954 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643170 | ACCACGTAAAAGATA[C/T]TACACACACACACGA | 5521 |
rs533410800 | snp | A/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608908 | AAAAAAATAGAGGAG[A/G]GAATACTTCCAAACT | 5521 |
rs533412517 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930695 | ATTAAAAATGCAGAA[-/G]GAAAAAGCTTGTACC | 5521 |
rs533413703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992694 | TCATTACAACATAGT[C/T]GGGATAAAGTCCTGG | 5521 |
rs533415212 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976603 | TCTTTCTATCAATTT[G/T]TAACATTATTTTGTT | 5521 |
rs533433470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146749767 | CCATGCCCGGCTAAT[C/T]TTTTGTATTTTTAGT | 5521 |
rs533440154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714047 | AAGAGGACCAAGAGC[C/T]GAACAGTAGGGCACT | 5521 |
rs533447114 | snp | G/T | | | intron-variant, downstream-variant-500B | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146617007 | TGGATAAAGAAAATG[G/T]GGTACTTATATACAA | 5521 |
rs533448247 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068079 | GTTTACTAAACTTAG[A/C/T]AAATATTAAATATTA | 5521 |
rs533452339 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871697 | TATATGTGGAGGGTG[A/G]AGCACAACTTGCATT | 5521 |
rs533473684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693256 | GTCTCACTCTGTCAC[C/T]TAGGCTGGAGTGCAT | 5521 |
rs533483681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701006 | AGGCCTCCTTTAAAA[A/T]GTGAAGAAAATGGGC | 5521 |
rs533486234 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008642 | TCTAGCTCAAGAGTC[A/G]CCTCTTCTAAGAGGC | 5521 |
rs533486521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147074666 | CATTCTTATAATCTC[A/G]AATTTCTTAAACATC | 5521 |
rs533486975 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147067364 | TACTCTCTGGTTCTA[C/T]GTGCTTGACTTTTTT | 5521 |
rs533492182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914353 | GGAGAACATCCATGG[A/G]GTCCTTTGGGAAGCA | 5521 |
rs533494987 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002733 | TCACCAGGGTCCAGG[G/T]ACCATTGCGGGTTCT | 5521 |
rs533496881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757411 | ATTGTGGAACGGAGG[C/G]ACCACAGTAGGAACA | 5521 |
rs533503639 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714918 | TCCTTTTGAAGCTGA[A/G]AGCAGAAAGGACTCT | 5521 |
rs533520951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031355 | TTGTCTTTGGGGTTC[C/T]ATAATTTCATTTAAA | 5521 |
rs533536295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877415 | CGTGTCAGCCTCATT[C/T]GCTGCCCGCCAGAGC | 5521 |
rs533547344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838247 | AGAAATGTGAAATAC[A/G]GGGTGGTTAGGGGAT | 5521 |
rs533553737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146707704 | CTAACAGGTAAAGCA[A/G]TATGTACACTTACAG | 5521 |
rs533555671 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146921700 | TCTATATCAGTTCAT[C/G]TCTGCTTCTCTGTAT | 5521 |
rs533561148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146624342 | CTCGCTCTATGGCAC[C/T]TTCATCTAGGTGTGT | 5521 |
rs533566741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742553 | TTTTTCTGTTTTTGC[A/G]AATTTTTAATTCTCT | 5521 |
rs533579001 | in-del | -/TTTTTTTTTTTTTT | 0.350109 | 0.229081 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146938752 | GGTTAGATAATAGCC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 5521 |
rs533579787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147038253 | AGAGCTTACATTCTT[A/G]TAAGTTAAGCAACAA | 5521 |
rs533586653 | snp | C/T | | | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859171 | AGACAAGTTGATTAA[C/T]TCCACTGGATCTCAG | 5521 |
rs533590691 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030974 | GTGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 5521 |
rs533591604 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643731 | CACCTGTTCCTTAAA[A/G]CCTGTGGAAATAAAA | 5521 |
rs533611871 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968581 | TACTTCTTTGCTGAA[C/T]TGAAGTGTCAATAAT | 5521 |
rs533622605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618315 | AGGCAGGCAGCCTCT[C/T]GAAGCTCAAAAAGGC | 5521 |
rs533627154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146714459 | CTTTCACAGTGTCAT[A/G]GAAATAACAGCATGT | 5521 |
rs533630290 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147030066 | TATTAGAATTGCATG[G/T]TGCTGTATATCACCT | 5521 |
rs533631854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806680 | GGAGAAGAGTCAGCA[C/T]ACTGGAATTTTTGCT | 5521 |
rs533641157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700645 | TGTCCTCTTCACATC[G/T]GTTGGCAAATAAACT | 5521 |
rs533643667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146736775 | AAAAGCAGGATTGCA[A/G]CTTTGTGTTTTCATC | 5521 |
rs533664886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146844120 | AAAAAACCAAACACC[A/G]CATATTCTCACTCAT | 5521 |
rs533671395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850844 | CATAGCTGGTATACA[A/G]TAAGTGCCCAATAAA | 5521 |
rs533672367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146933917 | ATTCCCACCTATGAG[C/T]GAGAACATGCGGTGT | 5521 |
rs533675142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147061039 | GTTAAATTCTGACCT[G/T]AAAGAAAGAGGATCC | 5521 |
rs533681022 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147053649 | TCTGGTGGCAAAGTG[A/G]TGTGTTTGAGGAAAC | 5521 |
rs533681952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146895999 | ATTACTGTTTGACAA[G/T]TCATCGGGCTAAATA | 5521 |
rs533688235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715286 | ATTCCTTTCCTGCAG[C/T]ATGACTACAGGTAGA | 5521 |
rs533688672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785372 | GGCAACATAGTGAAA[C/T]GCTGTCTCTACAAAA | 5521 |
rs533695875 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146631670 | AAAATCAATTAAAGT[C/T]TGCTTTGTTCAGAAA | 5521 |
rs533717607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608007 | TAAAACACTATTCTT[G/T]TTTGATTTCTTCAAC | 5521 |
rs533729875 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146742791 | TGGGTCCTAATTCAA[A/T]ATGACTAGTGTCCTT | 5521 |
rs533731558 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146694356 | ATATTTATATAGTCA[C/T]GTGATTAGCTCTTGA | 5521 |
rs533734484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146989973 | TATCTGAAAAAGAAA[A/T]CAAGAAAGCAATTCT | 5521 |
rs533747180 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693965 | TCCTCTTTTGCCCCT[A/T]GCTCCATTCCTCCAC | 5521 |
rs533750748 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027832 | TAAATTATGTCCCAA[C/T]AAAGTTCATTTAAAA | 5521 |
rs533768210 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146860876 | ATAGTCTTAGCTTTC[C/T]TGTCGCAGCCAAGAC | 5521 |
rs533777051 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146845452 | TAGAGACGGGGTTTC[A/G]CCGTGTTAGCCAGGA | 5521 |
rs533777504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147068947 | TAATCAGAAAAATCA[C/T]TCATGAAACAATAGA | 5521 |
rs533779337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060714 | GTATAATAACCATTC[C/T]CAACATATACAGCTC | 5521 |
rs533784361 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813123 | TACTATGAATGAAGC[A/T]ATATATATAGTGTGT | 5521 |
rs533785092 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146880750 | GGAGAATGTCCCTTC[C/T]ACAGATCGAGTCTCT | 5521 |
rs533797209 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146956075 | AGCCACTGAGCCTGG[C/G]CCAATAGTCTTCTTT | 5521 |
rs533803117 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700620 | CATTTTCTTCTCTGC[A/T]GTCCCAAGTTGTCCT | 5521 |
rs533809817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771672 | CATGATTAGGTAGAA[C/T]ATTTGCTAGCTTCTC | 5521 |
rs533811135 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146847565 | TCCAGGAACCCACCA[C/G]AGGGCTTGTGCTCTG | 5521 |
rs533818574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832913 | CACACAAGGATGAAA[C/T]TGCCTAATGGCACAC | 5521 |
rs533819611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830429 | AAGCCCAACCAACAG[C/T]ACCCGAACCTTAAAT | 5521 |
rs533829908 | snp | A/G/T | 0.000135404 | 0.00822718 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146856452 | ATTTAACACTTCTAT[A/G/T]CTGCTACTTTATCAA | 5521 |
rs533846467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147054264 | GACAGGAGGACCAAT[C/G]AGAAATACAAAAGTC | 5521 |
rs533859132 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146818178 | GACTATTTGATCAAA[A/G]TACGTCTTTCCCGCC | 5521 |
rs533865084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146743464 | CAAAAGAAGGAAAAG[A/G]TGAGGTGGCTGCTAC | 5521 |
rs533866738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146890320 | GTCCTCCTGAGCCAC[A/G]GCTGTAGAGGTCAGG | 5521 |
rs533867940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146969859 | TGATGAGTTCTCTTT[C/T]AGATGGATTACATTT | 5521 |
rs533868883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883035 | AAACTTTTGGGTCAC[A/C]CTGTCCAATTAGCAC | 5521 |
rs533869075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618949 | CCACTTTGTGCTCAG[A/C]CATCTACAGTGACTC | 5521 |
rs533873201 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147002781 | TGCTGCTGCATTGGT[A/G]AGCACAACTCTTCTG | 5521 |
rs533875945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983467 | TTATAGGCGTGAGCC[A/G]CTGCACCCGGCCCAG | 5521 |
rs533879135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146701601 | AGCTTAGACATGGAA[A/T]ATGGAGGAACAGAGC | 5521 |
rs533885374 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146976909 | AAAACTAACAAGCAT[A/G]GAGATTAAAAGAACA | 5521 |
rs533885843 | in-del | -/AAC | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146876246 | TGGAATAAAAATAAG[-/AAC]AACGGTAATATCCAG | 5521 |
rs533886513 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146981215 | TCAGTTCTTCCCCTG[C/T]TTCATTCAGGGTTCA | 5521 |
rs533890347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146645221 | ATCTTTTTCCCTTTC[C/G]ATGGTCTAAATTTAA | 5521 |
rs533904414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779919 | GAAGTCTGCTTTTGA[C/G]TTACATATAGGGGAC | 5521 |
rs533905748 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146889916 | CATTAGGTCTAGCCC[A/G]TCATTTTGCTGATGA | 5521 |
rs533926299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792363 | TCTTCTGAGTCAATG[C/T]CACATTGTTCATGCA | 5521 |
rs533929283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147048032 | GATTCCTGGGGCCCA[C/G]TTCCAGGGGATTTAA | 5521 |
rs533931539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806154 | AGACAGTGTGTGTGA[C/T]GCGCACATACACACA | 5521 |
rs533937525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146737702 | ATCCCAGTGAAAAAA[C/T]TTATAAATGGGAAAC | 5521 |
rs533945745 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146968825 | GAGTTGAGGAGAGAC[A/G]TACAACATGAATGTA | 5521 |
rs533955666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639113 | TTCAAGTCACATGGC[C/T]AAGTGACAACACTAG | 5521 |
rs533959073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146877730 | CTGGGGTCATCTTTC[C/T]GGGCGAGAGCCCCAC | 5521 |
rs533959420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146650411 | AGAGTCTCATAGGTG[C/T]CAGTGTATTTTAAAA | 5521 |
rs533964241 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147008327 | GAGGAAACACAGGCT[A/T]ATGAAGGTCTATGCA | 5521 |
rs533968480 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146726250 | GTCAAACAAGCAGGA[A/C]GAAAACTAGGATTTT | 5521 |
rs533979518 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147063653 | TTTAATTAAATCATG[A/T]ATATTATGAAGAGGA | 5521 |
rs533986152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971978 | ATTACCTAAACTTCA[A/C]ATTTTATTTGGATTT | 5521 |
rs533986714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146883683 | TCTAAGGTGGTTTAC[A/G]TGCTGTCTAGAGAAT | 5521 |
rs533988079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146922225 | CCCTTGGTGGTTAAG[A/G]TTAAACCTTTGCAGT | 5521 |
rs533991018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146791794 | TTTATTATACCAGAC[C/T]ACTGGCTGTCTCCCA | 5521 |
rs533994490 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147016928 | TTGGCCAAGTTACAG[A/G]ATATCCTACATGTCA | 5521 |
rs534033761 | snp | A/C | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146615645 | TTAAACCCATTTACA[A/C]CAGCTACAAATTAAA | 5521 |
rs534036105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773435 | GTTTATTATGATCTA[A/G]ATTTGAATTAAAGCA | 5521 |
rs534045015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146857757 | CAATGGCACGATCTC[A/G]GCTCATTGCAACCTC | 5521 |
rs534054941 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147082860 | TTTGGAAGGCTGAGC[C/T]GGAATACAGTTTCAG | 5521 |
rs534071378 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785650 | ACAAAGGCAAGCAAC[A/G]GAACTAAAATAATAA | 5521 |
rs534073384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146871068 | CTGCGAGATAGTTAT[A/G]TTGGGGCTGACTTTC | 5521 |
rs534076209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998048 | ACTCCTTCTCACAAG[C/T]GTGCAGAGGGCTCCA | 5521 |
rs534087890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146662858 | AGACAAACAGCTCAG[G/T]AAAAATATGGGCAAA | 5521 |
rs534089797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146914586 | CTTAAAATCTGGGAA[C/T]CAATTAGGCATTCAT | 5521 |
rs534093138 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146984995 | CTTTATCAGATGTAT[A/C]GTTTGCAAATATTTT | 5521 |
rs534099885 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146655793 | GGCACTGCCCAGGCC[A/G]TATGAACCAAACGGG | 5521 |
rs534103778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832458 | GTGCAGTGAAGCGAT[A/G]TTGGCTCACCGCAAC | 5521 |
rs534113122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766734 | AATGCTACCACAACA[C/T]CGTGGGCCCTACGGC | 5521 |
rs534117410 | in-del | -/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639329 | GTTTTATCATCTGGG[-/T]TTTTTTTTCTCAGTA | 5521 |
rs534132194 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146887179 | AATAAAGAATTACTA[A/G]TGACATATCTAAATT | 5521 |
rs534132331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146693513 | AGCCACCACACCCGA[C/T]CACAACTAGTATTTC | 5521 |
rs534134646 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147031347 | TGTGACTATTGTCTT[C/T]GGGGTTCCATAATTT | 5521 |
rs534138392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146607523 | CATACAATGCATAGC[A/G]TGATGAAGAATGAAA | 5521 |
rs534151795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997498 | ACATCCCTGACAATT[G/T]CAAGTACCCAACTTG | 5521 |
rs534153297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146858271 | TAATTCTAAACTCTA[A/G]GGTTGGGAGGGTAAA | 5521 |
rs534155266 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146664852 | TGTTGTTAGCAGGCC[A/G]GAAAACATTAATCTC | 5521 |
rs534158089 | in-del | -/AAC | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786903 | CTTTATAACGAAGCT[-/AAC]AACAACTCTTGTTAT | 5521 |
rs534158161 | in-del | -/GTGA | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147058152 | GATAGTAAATATTAG[-/GTGA]GTAAGTGAATCGATG | 5521 |
rs534160166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772750 | TATTTATTTATGCCC[A/G]TAAGTGAGGTTTCTT | 5521 |
rs534166254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146908944 | TAGCTGGGATTACAG[A/G]GGTGGGCCCTGGAGC | 5521 |
rs534172685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146765978 | CTTTTTAGACTCTCC[A/G]TTTATTATCATCTGG | 5521 |
rs534173359 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146997373 | GTATGAATGAGGGAA[G/T]CCAACTGGGCTGCCT | 5521 |
rs534174158 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147039293 | TTACTGATGTTCCCC[A/C]TGGCTATTTTCCCCT | 5521 |
rs534174356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146819843 | CAACTCCATTCACAA[C/T]AGCCAAGATAAGAAT | 5521 |
rs534176245 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146618000 | TGCCAGCCATCTCTT[C/G]CTCAATTCCCCTGTA | 5521 |
rs534179915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146752387 | TTCTCTTTGGAGACA[A/T]CTTCCCTGACCACCC | 5521 |
rs534185237 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147070025 | CAAACTCCTGACCTC[A/G]TGATCTGCCTGCCTC | 5521 |
rs534202712 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146731274 | GCCAGTTACTGGCAC[G/T]TAAAATGGCTGCAAA | 5521 |
rs534207935 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146801258 | GATCTGATGTACAGC[A/G]ATGTGACTATAGTTA | 5521 |
rs534210108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146605457 | TTCAGCAAAATGTTC[A/G]ACCTGTGATATGTCA | 5521 |
rs534212264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146633255 | ACACGGTTCTCCTCG[C/G]CATTTTGATTAAATG | 5521 |
rs534212397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146979231 | ACCTTCTTAATGTTT[C/T]TGTTCATTTACATTT | 5521 |
rs534213471 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688210 | AAATACAGATACTGG[C/T]ATTTATAATTATATA | 5521 |
rs534213759 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589143 | ATGTAAGTAGAAGAT[G/T]ATATGGAGCCATTTA | 5521 |
rs534225317 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147041185 | GCTCTGCAAGATGGT[-/G]GGGCAGGATCTAAAA | 5521 |
rs534231047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978382 | TAGGTTAATTAGATC[C/T]CATTTGTCAATTTTG | 5521 |
rs534236515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147032339 | ATGCAAATCAAGACC[A/G]CAATGTGATACCACC | 5521 |
rs534242919 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146688611 | CCCAGCCACACCTCA[A/G]GGCCTCCTTCTCTGT | 5521 |
rs534243414 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146602589 | TTCTTTCCTGCCTGC[C/T]CAATGCACTCGCATA | 5521 |
rs534244871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146760222 | CCAAGTGCTTTATAT[A/G]TACCCTCTTAATATT | 5521 |
rs534247753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146846415 | TCAGGCACAGTGGCT[C/T]ACGCCTGTAATCCCA | 5521 |
rs534251282 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813242 | TAATCATTAAAAAAA[A/C]CCCCTCTCTTTACAC | 5521 |
rs534269343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146941556 | TTATGTCATCTGTAG[A/G]AAAACTAAAAAACAT | 5521 |
rs534292978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146652401 | GAGTGTTCAACTGGT[A/G]AGCAGAACCAGACAC | 5521 |
rs534309599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147010685 | TTCACTTTGCTTGCC[C/G]GCCGCTCACCTACTG | 5521 |
rs534313544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146744846 | TTATCTCCTACTTTC[A/G]TGGTCATTCACAGCC | 5521 |
rs534317609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923670 | GTGTGGCAATTCCTC[A/C]AAGACCTAAAATCAG | 5521 |
rs534317993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146689480 | GTACAGGTTTGTAGC[C/T]GAGGACCAACAGGCA | 5521 |
rs534327575 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146910552 | ACCATTAGTTGCCTC[A/G]TCTGCAAAAGGGTGA | 5521 |
rs534330443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793984 | CAGTAGATATTGAGT[A/G]GAGCTCAGAAATTTC | 5521 |
rs534340051 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648896 | ACTGGATAACAAAGA[C/T]GGAGACAGGTTCCAG | 5521 |
rs534344794 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146990641 | TAGGGGAAATGCTTC[A/T]TGAAATTGGAGTAGG | 5521 |
rs534344858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146725427 | AAAAAAATAACCAGC[C/T]ATAGGGAAATGGATG | 5521 |
rs534355289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146971974 | TACTATTACCTAAAC[C/T]TCAAATTTTATTTGG | 5521 |
rs534378802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147025449 | ACGCTAAAGTCACGC[A/G]AAGACATTACAAATA | 5521 |
rs534393429 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659680 | CCTTATGAAGTAGGT[-/A]ACTAAGATCATTGTC | 5521 |
rs534394891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828178 | TCCATAATGCACATT[C/T]TCTAGTTGAAGGTTT | 5521 |
rs534404495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146807739 | CACCAGGGATATGCC[C/T]TCTCCAACTCCTTGG | 5521 |
rs534411566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146702841 | TCTAGTTCATTTTCT[C/T]GAGAAGACTCCAGTG | 5521 |
rs534415546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146626396 | CCACAAATGGAAAAA[C/T]GGTCATAAAACACAG | 5521 |
rs534418717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146657652 | CCTGAATCTTACTAA[A/G]GTGTACTATGCAATT | 5521 |
rs534424421 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147060444 | CCAGCCTGGGCAATA[G/T]GGTGAATACCCACCT | 5521 |
rs534426141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917212 | CCTGTAATAACCAGC[A/G]ACATGGGCTCTACAC | 5521 |
rs534435678 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667938 | GAAACAAAGTGGGAA[A/G]AAGGAAGCATCAGAG | 5521 |
rs534438990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147004535 | AGCCTATAACCAGGT[A/T]TTTCTCCCACTTCCT | 5521 |
rs534451258 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147043418 | GAGAAAAGACCACGT[A/G]AGGACTCAGTTGAGA | 5521 |
rs534470249 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146885970 | GCCAGGGACTGAGGA[-/T]TAAAAAAAAAAGGGG | 5521 |
rs534476302 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146798065 | TGTCTTATTTTTAGT[-/CTC]CTCCTCAGGAGCTTT | 5521 |
rs534479776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146717697 | AGGTCATCATTAAGA[A/G]CACTTTGTGAACGGG | 5521 |
rs534480501 | snp | C/T | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146595319 | TAAAGGTATATAAAC[C/T]GGGCAGTGGCAAGGT | 5521 |
rs534483344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774833 | AAAAAAAAAAAAAAA[A/G]AAAAGAGAGAGAATA | 5521 |
rs534495863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005242 | CCTTAACCTATATAC[C/T]GGTGGAAGTTCATTT | 5521 |
rs534502160 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146627137 | GCTTTTGGCTTTTCT[C/T]CAGAGTGGGAAGTGT | 5521 |
rs534502289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590757 | CGTGCACGAACCCGG[A/G]GCGCGACCTCTCCCC | 5521 |
rs534523639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147005097 | TTCAAACATGTATGT[A/G]TGAGGCCCTCAACCC | 5521 |
rs534523790 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799132 | TCTTAGATGGAGTTA[C/T]GATTTCTTCACTAAA | 5521 |
rs534525019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147069935 | AGCTGGGATTACAGA[C/T]GCCTGCCACCATACC | 5521 |
rs534528319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146929192 | CCCACATTTCTGTTC[C/T]TTTCACAGCATATTA | 5521 |
rs534530950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146751713 | GCCTTGTGTGATGAG[C/T]TCTATGAAGAAATAT | 5521 |
rs534531303 | snp | A/C | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146978704 | GTGTTATTCCTGAGG[A/C]CTTTTTTCTGTCCTA | 5521 |
rs534543765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781265 | ACAGTAGTGTGAGTA[C/T]ATCAACCCAGGTCTA | 5521 |
rs534551431 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146670053 | AATTATGACACTTTT[A/G]TATCTTTCAGGTTGT | 5521 |
rs534556777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147034601 | GTAAAGTTTAAAATC[C/T]GTAATTTTTTCCCTA | 5521 |
rs534561733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672193 | GGAGGCAAGAGGAGA[C/T]GTAAATTTCCCAGGG | 5521 |
rs534569440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808875 | TCTCTATAGGACAGA[C/T]CGTCTGCAGGTTTCT | 5521 |
rs534569486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815769 | GTCTCAATTATATTC[G/T]TTACAAATGCTAACT | 5521 |
rs534600008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833748 | GCCCTTCCCCATCCC[A/G]TCCTCCTCCCCCACC | 5521 |
rs534609251 | snp | A/C | 9.88354e-05 | 0.00702908 | missense, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146590096 | TCCGCTTGCCCCCCA[A/C]ACACACTTTTCGGGG | 5521 |
rs534620422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:146879223 | AAAGTGGGAAGTGCC[A/G]CTCAGAGCCTATCTT | 5521 |
rs534628419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146815147 | TGCATGCTGGCACTG[A/C]CTACACTAGTCTGCT | 5521 |
rs534645403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146923350 | CAGAGCCTAAGTAGA[A/G]CTGGATTGCATGATG | 5521 |
rs534646823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146904722 | CCTTGAGAGAAAAGC[A/T]GAAACAGTTAAGAAC | 5521 |
rs534649639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146964419 | TTGACTTGGTGCTTC[A/G]CAGATTTTTTAACCT | 5521 |
rs534654252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146992807 | TTATAGGTGAAAGCA[C/T]AGGCTCTCCACTCAG | 5521 |
rs534654287 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146727165 | AGTGACAAGAACAAG[C/G]TCTCATTGTATTAGC | 5521 |
rs534657370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146608685 | CTATAGTCCCAGCTA[C/T]CTGGGAGAAGAATCG | 5521 |
rs534663809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078662 | TTAAAAAAAAATAAG[C/T]TGGGCATATTTGGTG | 5521 |
rs534669303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147056447 | TCTGTGCTCCACTAC[C/T]GCCTCTTTCTTCCCC | 5521 |
rs534670396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146696115 | TCCTTGAGTTTTTTT[G/T]TTTTTTGAGATGGAG | 5521 |
rs534672737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739137 | TGATCCCCCATCCCC[C/T]GAACCTCTTGAGTAG | 5521 |
rs534678143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147049503 | TTGGAGTTGGATATA[C/G]AAATTAAATCAATGA | 5521 |
rs534678957 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146620435 | CCAGCAGGCAGCCGT[A/T]AGGGAGGCGGCTGCA | 5521 |
rs534691586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146930769 | TCATTCTTGTTGAAG[A/C]CTAAGCTCATTTCTC | 5521 |
rs534693783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827266 | TATGCTCCTAAGTGA[A/C]TTTATTTTATTTCAG | 5521 |
rs534697185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146809568 | GAAGACCCTCTCTGA[A/G]GAAATGACGTATCAG | 5521 |
rs534705465 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146700506 | AGCACTCAGCTCCAG[A/G]GCCCTCTGTGTCACC | 5521 |
rs534705481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146705416 | GTCACTTCTAGGCTG[C/G]GGTGCCATGATTAAT | 5521 |
rs534706194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146780567 | ACAATTATCTTTGGC[A/G]TATTCCCCTTTCCAG | 5521 |
rs534709166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147027548 | TGAGGCAGGAGAATC[A/G]CTTGAACCAGGGAGT | 5521 |
rs534711217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147035298 | AGGTGCCACACTTTT[C/T]AACCATTAGATCTCA | 5521 |
rs534724783 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146672053 | TATAAGTGGTGAAGA[C/T]GGAAGCCAGGCTGCT | 5521 |
rs534743566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146745826 | AGCCAGGCATGGTGG[C/T]GCATGCCTATAGTCC | 5521 |
rs534749366 | in-del | -/GTGGTAGTAATAGTA | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146733937 | GTAGTAGCAGTGGTG[-/GTGGTAGTAATAGTA]GTGGTAGTAATAACA | 5521 |
rs534765550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146859361 | TAGCTGCTAATGTAT[A/C]AACCTGTTTGGAGAA | 5521 |
rs534770431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146866793 | CAGTATATAGTGGCT[C/T]TTCCTCATGATCATA | 5521 |
rs534776345 | snp | C/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146893645 | ACGGTGAAAACCCGT[C/G]TCTACTAAAAATACA | 5521 |
rs534787623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146795748 | TTCACTAGGTATAGT[A/G]TATCAAAACGTCAGG | 5521 |
rs534795580 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628022 | CAATCTCAGCTCACC[A/G]CAACCTCCACCTCCT | 5521 |
rs534797037 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951639 | TCCTGTGTTAGTTTG[C/T]TGAGGATAATGAGTC | 5521 |
rs534798593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146943554 | TAATGTGTTTTCTTT[A/G]AATTGCAATCTTGGC | 5521 |
rs534805199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146973464 | ACTTCAGCAGCAGCC[A/G]AAGGGCAGCGTGGCC | 5521 |
rs534810777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840978 | ATATGTATTAAACAT[C/T]AGTGGCCAATATGCT | 5521 |
rs534811254 | snp | A/G | | | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861487 | TGAGCCACCGCGCCC[A/G]TCGTCAAACTAATGT | 5521 |
rs534814782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146732716 | ATGCAAATCAATAGA[A/G]GAGGAATACTACTAA | 5521 |
rs534821337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071815 | TTGTCTAGCCCCTCC[A/G]CTATTGAATCTCCAG | 5521 |
rs534834156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146634580 | CCTTGGGTGATCTGC[C/T]CGCCTCAGCCTCCTA | 5521 |
rs534835304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146998978 | GAGATCAAGCCACTG[C/T]ACTCCAGCCTGGGAG | 5521 |
rs534861770 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146680275 | TTGGAAATCATCATT[C/G]TCAGTAAACTATCGC | 5521 |
rs534864393 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146835916 | AATGAAGTGGGTTGG[C/T]ATCCCAGTTCCACCG | 5521 |
rs534864482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951221 | GAGGTATAATATACA[A/G]TAGAATGTATGCATT | 5521 |
rs534866891 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710971 | CCATATTTTGGGACT[-/G]GCTCAGGTATCACTT | 5521 |
rs534869808 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146757405 | GTGAGGATTGTGGAA[C/T]GGAGGGACCACAGTA | 5521 |
rs534870831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146874185 | CTATATATTTATTTG[C/T]AAAATTATTTGTCTC | 5521 |
rs534881837 | snp | G/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146710881 | ATCTGGCACATGTTT[G/T]GTCAGAAATTTTGCT | 5521 |
rs534884272 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146739881 | ATGTCTGTGGGAATC[C/T]TTTGTAGATTTGAGG | 5521 |
rs534885261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603488 | AAGATGGATGTGAAA[G/T]GAAAGATGACAATTC | 5521 |
rs534888667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146653924 | GCTTGTCTGCTGCCC[A/G]GTGACTCCCCTCACA | 5521 |
rs534893530 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:147015768 | TATAATATAATATAA[A/T]ATAATGTAATATACA | 5521 |
rs534903231 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146649606 | CCCGCCACCATGCCT[A/G]GCTAATTTCTTTTTT | 5521 |
rs534903987 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925032 | CAGAAAATACAAGAA[C/G]TTTGCTCCAATATAC | 5521 |
rs534907764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147078322 | CCTGCAACTGGTAAG[A/T]CCTATAGTTAGAGCA | 5521 |
rs534913265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146639929 | TGGACAACAATGTAT[G/T]GAATCAACAAGCAAT | 5521 |
rs534918304 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146715077 | TAACTTTCACCAGTA[A/T]CCTTAATATCTTATA | 5521 |
rs534919767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775242 | ATGTAAAAATTCTCA[A/G]CAAAATACTAGGAAA | 5521 |
rs534929702 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PPP2R2B | GRCh38.p7 | 5:147057345 | AACAGTGCCTAAGTG[G/T]TCTGGTTTGTTTTTG | 5521 |
rs534934632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853191 | CTAATGTGTTGAGGC[A/C]ATAGAATTAGAGGCA | 5521 |
rs534938906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146966275 | GCAGGTAAGGAAATC[A/C]CGGAGGTTATGTCAG | 5521 |
rs534943270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146952767 | TCTGGTGATAGATTA[C/T]AGCTAAGGTCAGTGG | 5521 |
rs534947508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146960524 | CAAACTCCTGAACTC[A/G]TGATCCACCCGCCTC | 5521 |
rs534957525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146706117 | CTCAGGTAAGTCTCC[A/T]GTTCCCTGTGCTTCC | 5521 |
rs534959948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146830089 | TGCTCAATAGATGTT[C/T]CTTTTTTATTCTTAT | 5521 |
rs534966203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146898281 | CATTGATCTATATCT[C/T]TGTTTTGGTACCAGT | 5521 |
rs534968249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147071329 | AATAACCTTTCAACC[A/G]ATTCCTGCTTCTGAC | 5521 |
rs534969952 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804707 | TGATATTATTATATA[C/T]TAGACATGAATCTCT | 5521 |
rs534970345 | in-del | -/GAAGT | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146589743 | TTTCAATTCTAAACA[-/GAAGT]GAAGTGTCCCAAACC | 5521 |
rs534971248 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147051670 | AACAGGCCCTCCAGT[A/G]CCTGGTGCCAAATTA | 5521 |
rs534977422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146697295 | ATGGCTTCTTTTAGC[A/G]AGGATTTAAGAACCT | 5521 |
rs534987581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146666198 | TGTGTATATTACTGA[A/G]TAATATGTCTAGTGT | 5521 |
rs535004243 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146951309 | CCAACACAGTTAAGA[C/T]ATAGAACATTTCCAT | 5521 |
rs535008089 | snp | A/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808579 | ACTGGGAGTCCTAAA[A/T]CTTGACCCTGACTTC | 5521 |
rs535013859 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146897678 | CATATACTGGAGACA[A/G]CAGGGATACTTTTAG | 5521 |
rs535014370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937311 | GTCTCAGAAAAAAAA[A/C]AAAAGGGGGGTTACT | 5521 |
rs535020027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146616640 | AGAGCTCAACATCAC[C/T]GATCATTAGAGAACT | 5521 |
rs535028530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146621489 | AGAACAGACACTGGC[A/G]GCCCCACACCTCTGA | 5521 |
rs535038611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146861465 | CAAAGTTCTGGGATT[A/G]CAGGCGTGAGCCACC | 5521 |
rs535039143 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146690808 | TGGATTCTCATCCCT[G/T]TACCTTCAGTACAGA | 5521 |
rs535042442 | in-del | -/AT | 0.0126979 | 0.078662 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147009688 | AAGATATCACTTCAC[-/AT]GTTTTCAATTCATTT | 5521 |
rs535045228 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PPP2R2B | GRCh38.p7 | 5:147012257 | GCCACAATTTCGGAT[C/T]CTGTTATTGGTCTAT | 5521 |
rs535047177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146853924 | CTCTGAGCCCTCTTA[C/T]GTCATTTCACATTCT | 5521 |
rs535048983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146659134 | TTTGACTTAAAAAAA[A/T]TTTGTTCACATATTC | 5521 |
rs535062698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146994288 | GAGGTAATAACTTGC[A/G]TAACCCAGCAAATAA | 5521 |
rs535067277 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146772021 | ATTTTCATGGGTGTT[C/T]GTTGCAGCATTGCTT | 5521 |
rs535067974 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788746 | TCAACAACACAACAA[C/G]AAAAATTATGGTGAA | 5521 |
rs535078083 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146769153 | AAAGTGCTGGGATTA[C/T]AGGCCAGGCAAAGCT | 5521 |
rs535080981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146841603 | GAATACTATGCAACC[A/T]TTAAAAAGGATGAGT | 5521 |
rs535081946 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146983943 | CCCTTTATTCTTTCT[A/G]AACATTTTTATTATA | 5521 |