SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs744699 | snp | A/C | 0.438246 | 0.16451 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429046 | TTTGGCAACTCTGCA[A/C]CTCTGCCATTATAGC | 5522 |
rs755403 | snp | C/T | 0.493477 | 0.0567349 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387915 | ACCAATTATCATTCC[C/T]TACTTAGAGACAAGG | 5522 |
rs768636 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556082 | AGCCTCCTGCGTGAA[A/G]GATGCCTCTGGGGAG | 5522 |
rs872858 | snp | C/T | 0.25801 | 0.249872 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389318 | GGGGGACTTGCTCCC[C/T]TCGTCCATCACCATA | 5522 |
rs872881 | snp | C/T | 0.243633 | 0.249919 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463074 | TCAAAAAAGTTTTGA[C/T]GCAAACTTTCAAATT | 5522 |
rs872882 | snp | G/T | 0.407158 | 0.194426 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463001 | TTCCCCCCTCCCTCT[G/T]TCCCAGAGAAGGGAG | 5522 |
rs872883 | snp | A/C | 0.473461 | 0.122236 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462820 | CTCCCCTGCTTTTGG[A/C]TGAAGAATTTTTAGG | 5522 |
rs875579 | snp | A/G | 0.424503 | 0.179021 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6561216 | GGAAATGCCTGACTC[A/G]ACACTCAACTTCCCT | 5522 |
rs875864 | snp | G/T | 0.492287 | 0.0616198 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384955 | TTTCATTATCTGTAG[G/T]GTGCTTATGGTGGAG | 5522 |
rs878281 | snp | G/T | 0.462034 | 0.132445 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6420749 | GGCTCCATTGTCTCA[G/T]GTTTAACCAGTCCTC | 5522 |
rs878282 | snp | C/T | 0.189261 | 0.242509 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6420730 | TAACCAGTCCTCTTA[C/T]TGGGCATCAGCTTTT | 5522 |
rs878283 | snp | A/T | 0.470521 | 0.117772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6419942 | TCCAATATGACCTCA[A/T]CTTAACTAGTGACAT | 5522 |
rs1000647 | snp | C/T | 0.265453 | 0.249522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444862 | CCATGGATGTGAAGG[C/T]GAACACATGGAAACG | 5522 |
rs1985413 | snp | C/T | 0.410061 | 0.192043 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6448235 | AGGGATCAAACAGTT[C/T]TTAAATCCTGCAGCG | 5522 |
rs2019126 | snp | C/T | 0.151668 | 0.229849 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428867 | CAGGAAGTGGCAGAG[C/T]GGGTTTCGAACCCAG | 5522 |
rs2240264 | snp | A/G | 0.409721 | 0.192325 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6391152 | CCTGGGTTCCTGGGT[A/G]TCCAGGTTACGTGGG | 5522 |
rs2240265 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390993 | TGGCCACACTGTCCC[C/T]ACTCTCCCCACCCAA | 5522 |
rs2240266 | snp | G/T | 0.368938 | 0.219895 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390916 | GCTGCAGGAGGAAAC[G/T]TCTCACCAGGCCCGC | 5522 |
rs2240267 | snp | C/T | 0.371987 | 0.218218 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390910 | GGAGGAAACGTCTCA[C/T]CAGGCCCGCTGGAAG | 5522 |
rs2240268 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390615 | CGTCACTCACTCAGT[A/G]CTGATGTCCAGTCCC | 5522 |
rs2269920 | snp | A/C | 0.434109 | 0.169127 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321727 | CTGAATCAAAATGCC[A/C]AACTACGTGGCTCTG | 5522 |
rs3138737 | microsatellite | (TG)21/22/23/24/25/26/27/28/29/33 | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414071 | AACATAAGTTTTGCC[lengthTooLong]TACAGGTAAATAAAC | 5522 |
rs3220841 | microsatellite | (CA)20/21/22/23/24/25/26/27/28/32 | 0.830862 | 0.0643495 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414073 | TTATTTACCTGTATA[lengthTooLong]AGGCAAAACTTATGT | 5522 |
rs3222647 | microsatellite | (CA)14/18/19/20/21/22 | 0.627222 | 0.137262 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6559391 | agttCTGAAAAAATA[(CA)14/18/19/20/21/22]CAGNACAGAGGCAAA | 5522 |
rs3796398 | snp | C/T | 0.481473 | 0.0944461 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323058 | CCATTTTATGATTTG[C/T]GGCGGTGAACGCTTC | 5522 |
rs3796399 | snp | A/G | 0.00993419 | 0.0697739 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323062 | TTTATGATTTGTGGC[A/G]GTGAACGCTTCCTTT | 5522 |
rs3796400 | snp | C/T | 0.437683 | 0.165152 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323076 | CGGTGAACGCTTCCT[C/T]TCCTTTTTATTTTTT | 5522 |
rs3796401 | snp | A/G | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323151 | TGGGGCAGGGAGGGG[A/G]CCCAAACTTCCTGTG | 5522 |
rs3796402 | snp | A/T | 0.460902 | 0.134239 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323291 | TGGCAGGGGCCGGGA[A/T]CTGCACATACCTAGT | 5522 |
rs3796403 | snp | A/G | 0.465209 | 0.127221 | synonymous-codon | PPP2R2C | GRCh38.p7 | 4:6323359 | GTTGTTGGTGGCGGC[A/G]ATGGCAATGATGTTC | 5522 |
rs3924326 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495353 | GGGTGCTGGTCTGCA[C/T]GGGCCCCAGGCCTGC | 5522 |
rs3934547 | snp | G/T | 0.380529 | 0.213219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6516319 | GTCATCATCCTCTTT[G/T]CAGGCTGCAATGCCA | 5522 |
rs3934625 | snp | C/T | 0.318656 | 0.240388 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530338 | TTTCCATGCACGCGA[C/T]GTATGTAGAAGCGTG | 5522 |
rs3934626 | snp | A/G | 0.319136 | 0.24025 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530339 | TTCCATGCACGCGAC[A/G]TATGTAGAAGCGTGA | 5522 |
rs4074039 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477231 | ctccagcctgggcca[C/T]acagcaagattctct | 5522 |
rs4075006 | snp | G/T | 0.34101 | 0.232846 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6521549 | CACCCATTCAGTGTG[G/T]CTTCATCTCCCTGCG | 5522 |
rs4075007 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6521668 | TCATACGTAGGAGGC[A/G]CTTACACAGGAGCTG | 5522 |
rs4076080 | snp | A/T | 0.463451 | 0.130149 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6522041 | GTTTGGAAACAACAC[A/T]TCTCTGTTCCCAGAG | 5522 |
rs4076293 | snp | C/T | 0.203267 | 0.245593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506706 | tcagctaagcccagt[C/T]agtctgcccaaccac | 5522 |
rs4076353 | snp | A/C | 0.280785 | 0.248097 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6473086 | CCCGTTGGGAGCATT[A/C]AGTACATGTGAAGAA | 5522 |
rs4077345 | snp | C/T | 0.210605 | 0.246877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6471797 | TTTAAACCATTAAAT[C/T]TCCCCGAGATTTCTT | 5522 |
rs4234734 | snp | C/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6331403 | ATGAGGCAAAGCATA[C/T]TATGGACTTACCTCA | 5522 |
rs4234735 | snp | C/T | 0.188946 | 0.24243 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360456 | TTTCACCGAGCACAG[C/T]GAGGCTCATCCAGAT | 5522 |
rs4234736 | snp | A/C | 0.0872718 | 0.189788 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363122 | CAGCACCATGGACAG[A/C]GCCATGGCACGCAGG | 5522 |
rs4234737 | snp | G/T | 0.160609 | 0.233472 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363153 | AAGCCCTCAGTCATG[G/T]TGGAGGCTGACTGAC | 5522 |
rs4234738 | snp | C/G | 0.140919 | 0.224948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375986 | AGCAGCCGGATGGAA[C/G]AGAAGATCCACTTTA | 5522 |
rs4234739 | snp | C/T | 0.114036 | 0.209795 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6386026 | TAAGTGATTACTGTC[C/T]GCCAGGCCCTGCTCT | 5522 |
rs4234740 | snp | G/T | 0.0770498 | 0.180522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428100 | GCATCCCTAAGAGCC[G/T]CATGTCACAATCCAT | 5522 |
rs4234742 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462785 | GATGGAACGGGGAAA[C/T]GACAGGAGTCTTGGA | 5522 |
rs4234743 | snp | A/G | 0.089084 | 0.191327 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6474078 | GTAAATGCAAGGGCC[A/G]GAAGGATGTGCTTGT | 5522 |
rs4234744 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477895 | AGCCCTTCCCCTCCT[C/T]GAGCCAGCCTCCTCA | 5522 |
rs4234745 | snp | C/T | 0.436265 | 0.166749 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477966 | CCGTGTTCCCCTTCC[C/T]GGTTCAGATGTTTCC | 5522 |
rs4234748 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494514 | GAAGCACTGGTCTCC[A/G]AGACGGAGGGCCACC | 5522 |
rs4234749 | snp | A/G | 0.173643 | 0.238054 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494752 | TGCATGGGAAGGGAG[A/G]AGGCCATACTTGGCC | 5522 |
rs4234750 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495129 | TGCCAAGGGGCTACG[C/T]GGCCTCCACAGCCAG | 5522 |
rs4234751 | snp | A/G | 0.259397 | 0.249823 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6496929 | CACAGGGAGTGTGAC[A/G]ATGCCATACGTATGG | 5522 |
rs4234752 | snp | C/T | 0.144969 | 0.226867 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497160 | CAGCACCATGAGCAC[C/T]GGCAGGACACCCAGC | 5522 |
rs4234753 | snp | C/T | 0.483541 | 0.0916089 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497484 | GAAAAGAAAAAAAAA[C/T]TAAAATCCCTACCTC | 5522 |
rs4234754 | snp | C/T | 0.120674 | 0.21395 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515559 | CTCATTTAGTCTGCA[C/T]GACAGCTCTTTGAGG | 5522 |
rs4234755 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515866 | ggaagctgggagagg[C/T]gaggaagaatcctcc | 5522 |
rs4234756 | snp | A/G | 0.159292 | 0.232964 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530610 | CCAGCCCAGCAGTCC[A/G]GCTCAGAGTCACACC | 5522 |
rs4234757 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530795 | TAGTTGGGATGGCCA[C/T]TTACAGTGGTCGCAG | 5522 |
rs4234758 | snp | C/T | 0.488606 | 0.0746142 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6540088 | ATAAGCCATATACCA[C/T]ACACTTTACTTTTAT | 5522 |
rs4234759 | snp | C/T | 0.107694 | 0.205546 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6546963 | AAGAGCAACAGCTAA[C/T]GGCCCCCAAGCACAG | 5522 |
rs4247203 | snp | C/T | 0.434253 | 0.168969 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6349765 | TAGTAGTGGCGTATG[C/T]CTGTAGTCCCAGCTA | 5522 |
rs4247204 | snp | A/C | 0.0984431 | 0.198823 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6349781 | CTGTAGTCCCAGCTA[A/C]TCAGGAGGCTGAGGC | 5522 |
rs4263452 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468072 | TCTTACTAGGAACCA[C/T]ATGTGTTCTCCTTGG | 5522 |
rs4270639 | snp | A/G | 0.394171 | 0.204242 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390008 | GCCCCACCCACGTCT[A/G]TGAAAGAGACCCTCA | 5522 |
rs4272077 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6449097 | AAACACATAGCCCCA[C/T]GCAGGCATCACACAC | 5522 |
rs4272078 | snp | C/T | 0.164546 | 0.234942 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367657 | GGCTGCTATCAGTCC[C/T]CATCGCAGCACCTGC | 5522 |
rs4277850 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456946 | GGTGCGGTGGCTTGC[A/G]CCTATAATTCCAGCA | 5522 |
rs4282260 | snp | C/T | 0.406814 | 0.194704 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409866 | TGCCCAGACTTTCCC[C/T]TCTGCCTGGAACACC | 5522 |
rs4282261 | snp | C/T | 0.141258 | 0.225111 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358184 | AGAAATAACACCACA[C/T]ATCTACAACCATCTG | 5522 |
rs4293851 | snp | G/T | 0.130008 | 0.219321 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375124 | AAACTTTCTTGGGAC[G/T]GGGGGTGGGGCAGGG | 5522 |
rs4302525 | snp | C/T | 0.25634 | 0.24992 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6550474 | CCTACAACGCCAACC[C/T]GAAACACGTGCTGTT | 5522 |
rs4312829 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6443209 | AGCCTTCCAGGCAGG[A/T]GCCCGGCCGCCGCCT | 5522 |
rs4312830 | snp | A/G | 0.140919 | 0.224948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358094 | CAAACTATGCTACAA[A/G]GCTACAGTAACCAAA | 5522 |
rs4321706 | snp | A/C | 0.495368 | 0.0478996 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463793 | TGGACCACGTGTCCA[A/C]TTGTGGCCTCTGCCA | 5522 |
rs4323180 | snp | G/T | 0.404035 | 0.196909 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390092 | AAAAGGGTCTGGAGT[G/T]TGGGGTCTGATTCTG | 5522 |
rs4324617 | snp | A/G | 0.347032 | 0.230401 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425220 | ACCCTATAATTCCCT[A/G]TCCACCTGTCGGCCC | 5522 |
rs4327561 | snp | A/G | 0.408871 | 0.193029 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6379596 | CGCATCAACCAATCC[A/G]ATCTCTTTCTGCAGC | 5522 |
rs4331842 | snp | C/T | 0.499642 | 0.0133738 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6480054 | GAGACCACAGAGATA[C/T]GGCTGAAGTTCCTTT | 5522 |
rs4334819 | snp | A/G | 0.356169 | 0.226336 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429689 | AAAAGCCAATTTTAT[A/G]ACCGTCTCAGAGTGT | 5522 |
rs4336297 | snp | A/G | 0.473909 | 0.111197 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458635 | AGGCAGCACAACTAC[A/G]TGCTTTGCTGTCTGT | 5522 |
rs4342255 | snp | G/T | 0.232943 | 0.249417 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532417 | GGGGTGCCCCAGTCT[G/T]GTCTGGGATGGGCAG | 5522 |
rs4342256 | snp | A/G | 0.387642 | 0.208697 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532218 | ATGACCAAGGCAGTC[A/G]TGAGGACCATAGATC | 5522 |
rs4345249 | snp | A/G | 0.447809 | 0.152878 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425343 | TGCACCTCACCTGCT[A/G]TGTGTCCTGGGCACC | 5522 |
rs4346716 | snp | C/T | 0.499703 | 0.0121769 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6561722 | AGATACATACATGGA[C/T]ACATACACACACTGG | 5522 |
rs4352545 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506730 | tagctgagctgttcc[C/T]tcttggtgttcctca | 5522 |
rs4356980 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384016 | CAGATGCACATGTCA[C/T]TGAACTTAAAAAGAC | 5522 |
rs4358467 | snp | A/C | 0.320335 | 0.239902 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6549122 | AGCCACTGGTCTAAG[A/C]CACCATCATTGCTCA | 5522 |
rs4370214 | snp | A/C | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6524096 | tgtctctactaaaaa[A/C]aaaaaaaatacaaaa | 5522 |
rs4374689 | snp | C/G | 0.499971 | 0.00379382 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6469302 | GGTGGGTATTCCAGG[C/G]AACAGCCATTGCAAA | 5522 |
rs4374690 | snp | C/G | 0.49645 | 0.0419827 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356862 | TCACAGCTGCAGCCA[C/G]CGGCATGAGACAGGG | 5522 |
rs4379121 | snp | C/G | 0.482905 | 0.0908579 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6418235 | GCTCAACCATTCAGA[C/G]CCACCTACCCACAGG | 5522 |
rs4379122 | snp | A/G | 0.345037 | 0.231231 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6526573 | CCCTCAACATGGAGC[A/G]TTCACGACCACCCCC | 5522 |
rs4380587 | snp | C/T | 0.266 | 0.249487 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556702 | TTGCCAACCCATGCA[C/T]TAGTGTAGATCCCTA | 5522 |
rs4382106 | snp | A/G | 0.0569829 | 0.158885 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383725 | GCTTTTATCATCTGT[A/G]GGCTCTCTTCCTGGC | 5522 |
rs4386674 | snp | C/T | 0.484138 | 0.0876334 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463928 | GTTCAAATCCCAAAA[C/T]CTCCTAAGTGTGGTG | 5522 |
rs4386675 | snp | A/G | 0.494315 | 0.0530107 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6350231 | GCTGATTTCTCCAGC[A/G]TCCACCTGGCAGCCC | 5522 |
rs4388152 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6472474 | gccggggcccaggcg[A/C]gcATCCCGGCCGGCC | 5522 |
rs4391116 | snp | C/T | 0.396546 | 0.202545 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389946 | TTATGGGGTCAGAGA[C/T]GGGAGGCTGAGGAGT | 5522 |
rs4397075 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6427633 | TTTCCAGACACCTCA[C/T]TTGTGGCCATGCTTG | 5522 |
rs4404623 | snp | A/G | 0.441568 | 0.160629 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458427 | TCGCTGCGTCCTCAC[A/G]TGACAGAAGGGCAAG | 5522 |
rs4404624 | snp | A/G | 0.401747 | 0.198678 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458812 | TTCAGAAAGGCCTGG[A/G]TTCCTGTCCTGTCTC | 5522 |
rs4419546 | snp | C/T | 0.401037 | 0.199218 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6543436 | AAAAACAACAACAAA[C/T]ACCAGGCCAGGCGTG | 5522 |
rs4431291 | snp | A/C | 0.497749 | 0.0334707 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463853 | CTCTCCTCCTGCTGA[A/C]CCCTCTCGATTGCCT | 5522 |
rs4431292 | snp | C/T | 0.0912534 | 0.193131 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383806 | CAAATGGTGCCTGTA[C/T]GCAGTAGCCAGGCCA | 5522 |
rs4432825 | snp | C/T | 0.403684 | 0.197183 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6499701 | TTCTGTATATAAAAA[C/T]TTGTAATATTTAAGG | 5522 |
rs4440300 | snp | C/T | 0.346811 | 0.230494 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6370731 | TGAAGCCACCTGGCC[C/T]GCAGCTCTCTTACAG | 5522 |
rs4441821 | snp | C/T | 0.446902 | 0.154045 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6472644 | cgccgccgccgccgc[C/T]gtcgcAGGCCCCTCC | 5522 |
rs4444913 | snp | C/G | 0.030665 | 0.119967 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463441 | TCCCATCCCTGCTTG[C/G]GGCAGCCCACACCCC | 5522 |
rs4469149 | snp | C/T | 0.347253 | 0.230308 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6426030 | GGCCTGCTTCCCTCA[C/T]GGCTCTGATCCCCCA | 5522 |
rs4484373 | snp | C/T | 0.206642 | 0.246211 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334239 | TGGCTGAGCCCTACT[C/T]ATAGGTGGGTTTTGT | 5522 |
rs4490526 | snp | A/G | 0.111224 | 0.207945 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6386247 | gctttcacagcctga[A/G]gacaagtcccagcct | 5522 |
rs4495116 | snp | C/T | 0.22263 | 0.248497 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360920 | GTGTCCTCACATTCT[C/T]ATTCCTGCATCTTAA | 5522 |
rs4505896 | snp | G/T | 0.446249 | 0.154875 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497389 | TATCAGGAAATGGCA[G/T]AGTACAGAGAGGATG | 5522 |
rs4507442 | snp | A/G | 0.353154 | 0.227726 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389875 | AGATTGGATTCCAGC[A/G]GTCTGCCTCCTGAGT | 5522 |
rs4522940 | snp | C/G | 0.409552 | 0.192466 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436933 | CTAACTTGGTTCACA[C/G]ATGGGCTTTGACCCA | 5522 |
rs4524456 | snp | A/G | 0.464096 | 0.129085 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6491012 | ACCTCTCCTGAACGC[A/G]GGGCACCACCCCACG | 5522 |
rs4526050 | snp | A/T | 0.449853 | 0.150196 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447152 | GCCTGGCTCTCACTC[A/T]CACCAAGGAGCCCCG | 5522 |
rs4538552 | snp | C/T | 0.311859 | 0.242226 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6529439 | GTTCCATGGGGCCCA[C/T]GCAGCTTGGCTCATG | 5522 |
rs4540117 | snp | A/G | 0.4944 | 0.0526182 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6500960 | GGAGAGGCAGGGAGC[A/G]GGAAGCCTCTCTGGG | 5522 |
rs4540118 | snp | C/T | 0.498009 | 0.0314867 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463647 | CTCAAGCAGAGGAGC[C/T]GGACACTGTCAGGGG | 5522 |
rs4543208 | snp | A/G | 0.344815 | 0.231323 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6327738 | TGCCAGCCCAGCCCC[A/G]GGTCGGGCCTCCATC | 5522 |
rs4543209 | snp | C/T | 0.297128 | 0.245518 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6328923 | ATGATGGTGACCGGG[C/T]GCTGGGCTATAGCCC | 5522 |
rs4547869 | snp | G/T | 0.370365 | 0.219117 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6330623 | ACCAGCCTGCCCGCC[G/T]GCTCTGCAGATTTAG | 5522 |
rs4554149 | snp | A/G | 0.135825 | 0.222405 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493858 | TAGCTTTAAAATCAC[A/G]CAGCCTCGGTGTATT | 5522 |
rs4554150 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6418867 | GCCCTGTACTAAGTG[C/T]CATGCCTGGTTCTGG | 5522 |
rs4561985 | snp | C/T | 0.0543475 | 0.155628 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421825 | GGTAACAGAATGAAA[C/T]AAGATGTAAAAAGGG | 5522 |
rs4561986 | snp | C/G | 0.0729998 | 0.176553 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6472890 | GAGAAGGCCAAGAGC[C/G]GGGGTGCTGGGAAGG | 5522 |
rs4563558 | snp | A/C | 0.327211 | 0.237778 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6547567 | GCTCAATCTAATAAA[A/C]GCTCTGCGGATTTCT | 5522 |
rs4565150 | snp | A/G | 0.49263 | 0.0602539 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515339 | AAATGCTCACCATCC[A/G]GTACTTGTTGAATGC | 5522 |
rs4565152 | snp | G/T | 0.159951 | 0.233219 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6351035 | GGAGGCCAGGCACCA[G/T]AGCTCACACCTGTAA | 5522 |
rs4566726 | snp | C/T | 0.496905 | 0.0392151 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6479962 | GCAATCCTCTCACCT[C/T]AGCCACTGAAGTAGC | 5522 |
rs4569820 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6448615 | TTTCCTCACTCCCAC[C/T]GCTGCCACACCCTGG | 5522 |
rs4571410 | snp | A/G | 0.110519 | 0.207473 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515278 | TCTATGAGAGTGTTC[A/G]GTTGTCAAACAAGAG | 5522 |
rs4580720 | snp | C/G | 0.356597 | 0.226135 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389763 | CAACTCCAAGATGTT[C/G]TTGTGTGCTGTTATC | 5522 |
rs4585379 | snp | C/T | 0.35809 | 0.225425 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374259 | CCGGCAACATTGCTT[C/T]CTGTTTTCTCCAGGC | 5522 |
rs4593210 | snp | A/G | 0.331411 | 0.236373 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388476 | AGTTAAGGTGCGGTC[A/G]TACTGGATTATGGTG | 5522 |
rs4594799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6467714 | ATGGGCTGCAAGTAA[C/T]GGAGACTTGAAAGTG | 5522 |
rs4596320 | snp | C/T | 0.339203 | 0.233544 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368004 | TTATGTTTTGATGAA[C/T]TAATAATCATTTTCA | 5522 |
rs4597907 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6557516 | GGACATGGAAGCTGC[G/T]ACCTGAAGGATGAGT | 5522 |
rs4604129 | snp | A/T | 0.477684 | 0.103247 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458397 | ccaacttcctgactc[A/T]caaacagtgccttct | 5522 |
rs4610412 | snp | C/T | 0.301177 | 0.244706 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6540674 | CCAAAGTGGCTACAC[C/T]ATTTCACGTTCCCAC | 5522 |
rs4616830 | snp | C/T | 0.469247 | 0.120128 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462443 | AAGATCACGCCATTG[C/T]ACTCCAGCCTGGGCG | 5522 |
rs4618386 | snp | G/T | 0.157311 | 0.232183 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387412 | tcagagactgctgac[G/T]tgtcagcagaaataa | 5522 |
rs4623093 | snp | A/G | 0.213333 | 0.247296 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6513340 | CACTGCTCCTTGAAA[A/G]GAAAACAGCATCTCT | 5522 |
rs4624724 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495651 | CCTGGAAATGGAGAT[A/G]GTAGGTCACTGAGCC | 5522 |
rs4631123 | snp | C/T | 0.499598 | 0.0141716 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6469318 | AACAGCCATTGCAAA[C/T]GCCCTGAAGCAAGAA | 5522 |
rs4688994 | snp | C/T | 0.352504 | 0.228019 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334400 | GGTCCCTAAAGGCAA[C/T]GGTTTGCTGCCCACC | 5522 |
rs4688995 | snp | A/G | 0.139564 | 0.224285 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6359200 | gtcctttgtagggac[A/G]tggatgaagctggaa | 5522 |
rs4688996 | snp | C/G | 0.497613 | 0.0344622 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6359440 | CATGGCACATGTATA[C/G]CTATGTAACAAACAT | 5522 |
rs4688997 | snp | C/G | 0.380179 | 0.213454 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375803 | GTGTGCCTGCTTCCC[C/G]CTCACCGGAGCTCAC | 5522 |
rs4688998 | snp | A/G | 0.0971971 | 0.197867 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375807 | GCCTGCTTCCCCCTC[A/G]CCGGAGCTCACCTGC | 5522 |
rs4688999 | snp | A/C | 0.489083 | 0.0730708 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382065 | GGCCTGCTCCACCAA[A/C]AAGTTTTACTGCAGC | 5522 |
rs4689000 | snp | A/G | 0.389887 | 0.207199 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413891 | TCATGATGCCCCACA[A/G]CCCCTGCTCACCCGT | 5522 |
rs4689001 | snp | A/G | 0.463989 | 0.129263 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414301 | CCTACATGTACGAAA[A/G]GAACCAGTTCCACTG | 5522 |
rs4689002 | snp | C/G | 0.372189 | 0.218105 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6426245 | TACTCATCACCCTAG[C/G]CAGCTGGGCAGTGAG | 5522 |
rs4689003 | snp | A/G | 0.483126 | 0.0902898 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6426569 | GCAATTGTGGTCCTT[A/G]TATTTCAGACACAAG | 5522 |
rs4689004 | snp | C/G | 0.300421 | 0.244863 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433368 | CCATTTCCAGTGGTG[C/G]CATGAGTTTCCATTT | 5522 |
rs4689005 | snp | C/T | 0.302184 | 0.244493 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433768 | ATGAAACAGGCACCA[C/T]TGTTACATCCATCTG | 5522 |
rs4689006 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434562 | tggggtttcgtgatg[C/T]tggccagtctggtgt | 5522 |
rs4689007 | snp | A/G | 0.485596 | 0.0836329 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444976 | GATCCCTTCAGCCTA[A/G]GGGTTCCAGATCAGT | 5522 |
rs4689008 | snp | A/G | 0.336474 | 0.234568 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6459248 | GTGGTGCTGGATATT[A/G]GGCAGGCAGCTCAAC | 5522 |
rs4689009 | snp | C/T | 0.428635 | 0.174898 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6465678 | AAAAGCTTAAACTCT[C/T]AGCGTGCATTTTATC | 5522 |
rs4689010 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6475023 | AGCATCTACTATGTG[C/T]AGGCATGTTCCCAGC | 5522 |
rs4689011 | snp | A/G | 0.376592 | 0.215579 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6486978 | caattattccattct[A/G]tctactttctggctt | 5522 |
rs4689012 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493109 | ATACCTGCAAGCCTC[A/G]GCCCCTCACTTTGCA | 5522 |
rs4689017 | snp | A/G | 0.336702 | 0.234484 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6539815 | TACAGGAGTCTCCCC[A/G]TACGACAAGTGAGGC | 5522 |
rs4689018 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6544739 | CTTCCTCTTGAAATA[A/G]AAACTGCTGGCCAGC | 5522 |
rs4689019 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6554934 | gaaggaaggaaggaa[A/G]gaaagaaagaaagaa | 5522 |
rs4689402 | snp | A/C | 0.314057 | 0.241654 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6325942 | CTACTTGGGAGGCTG[A/C]GGCAGGAGAAGTGTT | 5522 |
rs4689403 | snp | C/T | 0.313082 | 0.241911 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6326044 | ATCACAGTGCTCTCC[C/T]CGCCCCTTGGCCTGG | 5522 |
rs4689404 | snp | C/T | 0.483345 | 0.0897213 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6331399 | TTAGATGAGGCAAAG[C/T]ATATTATGGACTTAC | 5522 |
rs4689405 | snp | C/T | 0.356811 | 0.226034 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6333459 | TCTTCACCTACATAC[C/T]GGGCATATGAAAGCC | 5522 |
rs4689406 | snp | C/T | 0.293037 | 0.246268 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6336524 | GGCAGGAGGAGGGGG[C/T]TGCAGCCAGGCCTGG | 5522 |
rs4689407 | snp | G/T | 0.452597 | 0.146474 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6340013 | GGAGGGGCCTCCTGT[G/T]CGGCCTCTTTCCCTA | 5522 |
rs4689408 | snp | C/T | 0.311614 | 0.242289 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6340486 | AAAGCTCCACACAGA[C/T]GGGAGCCTGGTCTCT | 5522 |
rs4689409 | snp | C/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6340883 | cctctctccagcctc[C/T]gtatccagccacagg | 5522 |
rs4689410 | snp | A/G | 0.480461 | 0.0968913 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6342477 | CATGTGTTTGCACTA[A/G]GTGTGCAAAGAATGA | 5522 |
rs4689411 | snp | A/G | 0.460925 | 0.134204 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6342510 | TGCGGTTATTATTTC[A/G]CCCAACACCGGGCCA | 5522 |
rs4689413 | snp | C/T | 0.454302 | 0.144085 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6343256 | ACTCGCCCCAATGTG[C/T]GGCAAATTAAATGAG | 5522 |
rs4689415 | snp | C/T | 0.419456 | 0.183806 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6359905 | AAGAAGCATCACTGG[C/T]TGGTTCTGGCAAGGA | 5522 |
rs4689419 | snp | C/G | 0.498774 | 0.02473 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362209 | GGAGAGGAGTTCTAA[C/G]AGGGAGGGAGAGGCT | 5522 |
rs4689420 | snp | A/C | 0.17178 | 0.237664 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362491 | GACAGCCATGCTCAT[A/C]GCAAAACAACCTCCC | 5522 |
rs4689421 | snp | G/T | 0.188 | 0.24219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6364483 | gacatgatcttgtcg[G/T]ttttttttttctcat | 5522 |
rs4689422 | snp | A/G | 0.127254 | 0.217792 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6369623 | CTGCCTGCACCATCC[A/G]CAGTGCCACAGCTCC | 5522 |
rs4689424 | snp | C/T | 0.404209 | 0.196773 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375582 | GTGAAAAGCACTTTA[C/T]AGCCATACACCACCC | 5522 |
rs4689425 | snp | A/G | 0.477515 | 0.103619 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6376326 | TGAAAGGTACCCAAG[A/G]CCCTGCCATTAGGAA | 5522 |
rs4689427 | snp | G/T | 0.111576 | 0.20818 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6386409 | caagacagatcccca[G/T]agggggcaaataaac | 5522 |
rs4689428 | snp | C/G | 0.498832 | 0.0241331 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6386464 | CAAACCACACACACA[C/G]AGGACAGACTTCCAG | 5522 |
rs4689429 | snp | C/T | 0.314057 | 0.241654 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6393167 | CCAGAACATTCCCAC[C/T]GCCCCAAAAAGAAAC | 5522 |
rs4689430 | snp | A/T | 0.201418 | 0.245234 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6397858 | ACTTTGCAATAAATA[A/T]ATAAATAAAGGAACA | 5522 |
rs4689431 | snp | C/T | 0.164873 | 0.23506 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6398051 | attccacgaggaaag[C/T]acagtctttccaata | 5522 |
rs4689432 | snp | C/T | 0.334412 | 0.235318 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6398630 | aggtggagcaaacag[C/T]ccctcacacactgct | 5522 |
rs4689433 | snp | G/T | 0.425277 | 0.178263 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6398780 | tcacaaactcacaaa[G/T]gtgcatacgtacgtg | 5522 |
rs4689434 | snp | C/G | 0.499368 | 0.0177603 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404074 | CCCATCTCATGCTGA[C/G]GTGCTCAGCATTTGT | 5522 |
rs4689435 | snp | A/C | 0.362104 | 0.223456 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409978 | AGGAAGTAGAGTTTA[A/C]AGTGAGGAGCCAGTC | 5522 |
rs4689436 | snp | A/G | 0.29789 | 0.24537 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410614 | GTGCCATGCTGGCTG[A/G]TCTGCAGGTGTGTGA | 5522 |
rs4689437 | snp | A/C | 0.396364 | 0.202676 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413831 | GACTGTGCCGGGGCT[A/C]CCACTCAGGGCTGGC | 5522 |
rs4689438 | snp | C/G | 0.396364 | 0.202676 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413832 | ACTGTGCCGGGGCTC[C/G]CACTCAGGGCTGGCC | 5522 |
rs4689439 | snp | C/T | 0.117188 | 0.211804 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415331 | CATTTGGCAGACATT[C/T]AGCCTCTTATTTCAA | 5522 |
rs4689440 | snp | A/G | 0.361263 | 0.223876 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6419679 | tacacacagacagct[A/G]gaaaacaatcgaact | 5522 |
rs4689441 | snp | C/T | 0.422 | 0.181428 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6421007 | TCTCCTCGATGTGCC[C/T]GAGGAGGGCTTCGTG | 5522 |
rs4689442 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6427360 | AACTAACTCAACAAC[C/G]ACCTCCTTGGTCCTG | 5522 |
rs4689443 | snp | A/G | 0.429238 | 0.174281 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428265 | TGCCTCCAGGTTCCC[A/G]TCAACATGGCTGTGT | 5522 |
rs4689444 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433759 | CAACAACTTATGAAA[C/T]AGGCACCATTGTTAC | 5522 |
rs4689445 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454953 | AATAGTTATGCCTGC[A/G]GAGATAGGTGGTGCA | 5522 |
rs4689446 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455027 | CAGACACCTATCAAG[A/G]GATAATGAACACAGC | 5522 |
rs4689447 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455271 | AAAACACCTATAGCC[C/T]TACATCAAGAAATTG | 5522 |
rs4689448 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455394 | GTTCAGCAGTGGGAG[A/C]AGCTCTCTCTGTCCT | 5522 |
rs4689449 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455404 | GGGAGAAGCTCTCTC[C/T]GTCCTCCACCTGCCA | 5522 |
rs4689450 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455405 | GGAGAAGCTCTCTCT[A/G]TCCTCCACCTGCCAC | 5522 |
rs4689451 | snp | C/T | 0.468349 | 0.121752 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456825 | AACATCACTGTGGCC[C/T]GGCCACGTGGAGGGC | 5522 |
rs4689452 | snp | G/T | 0.254664 | 0.249956 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6459024 | ACCAGGAATTCAATG[G/T]CAGGAATCCATGACT | 5522 |
rs4689453 | snp | C/G | 0.38555 | 0.210062 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6459764 | TGCACTCCAGCCTGA[C/G]CAACAGAGCAAGCCT | 5522 |
rs4689454 | snp | A/C | 0.480461 | 0.0968913 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6459794 | TCTGTCACACACACA[A/C]AAAAAAACAGCAATT | 5522 |
rs4689455 | snp | C/T | 0.401924 | 0.198543 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464597 | AGACGTGAATTACAA[C/T]AAATATTTTTCATCT | 5522 |
rs4689456 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464782 | TCTGAAGAGCATCAT[C/T]CCAAGGTTAAGGGGG | 5522 |
rs4689458 | snp | A/G | 0.107694 | 0.205546 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6465485 | CCCAGAGTTCCAGCA[A/G]AGcagggccaaccct | 5522 |
rs4689459 | snp | A/G | 0.281841 | 0.247964 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6474991 | ACTTTCATTCATTCA[A/G]TGAGGAATGTTTATT | 5522 |
rs4689461 | snp | A/G | 0.106987 | 0.205054 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6475918 | GGCCATGAGGGTGGG[A/G]TCTTCATGGAGAGAT | 5522 |
rs4689462 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6481517 | ttccattggtctttc[C/T]gtctggcccatgtgg | 5522 |
rs4689464 | snp | A/G | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6481808 | acatgatgagacccc[A/G]tctctactaaaaata | 5522 |
rs4689465 | snp | C/T | 0.482905 | 0.0908579 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6489062 | agtctgcctgtgaaa[C/T]ccagccactttgatc | 5522 |
rs4689466 | snp | A/G | 0.494568 | 0.0518327 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6490104 | AGCCCCCAGGCATCC[A/G]TCCCTCCCACCAGCT | 5522 |
rs4689467 | snp | C/T | 0.493837 | 0.055168 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6501893 | TCTTTGTCTTTTTGG[C/T]CCCAGAGCTCAGCAG | 5522 |
rs4689468 | snp | A/G | 0.483708 | 0.088773 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6505827 | AAAAATTAGCTGGGC[A/G]TGGTGGTACACGCTT | 5522 |
rs4689469 | snp | A/C | 0.494526 | 0.0520291 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506114 | TCCTACTCACATGAC[A/C]TTCTAAAATAATGTG | 5522 |
rs4689470 | snp | G/T | 0.200182 | 0.244986 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515736 | ACTGCATGCCAGCAC[G/T]AAGTTAGGTGCTTGT | 5522 |
rs4689471 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530965 | TGTTAAGTGCAGCTG[C/T]GGCATCACTGTGCTC | 5522 |
rs4689472 | snp | A/G | 0.288127 | 0.247076 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531334 | CACAGAGGAAAGGAC[A/G]TCAGAGCCAACCCGT | 5522 |
rs4689473 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531444 | CGTCCAGGAGAGGGC[A/G]GCTACAACCGCCAGG | 5522 |
rs4689474 | snp | C/T | 0.157972 | 0.232445 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6533521 | CCAGCCATCCAGGGC[C/T]CAGCACCCCATGGCC | 5522 |
rs4689475 | snp | C/G | 0.103203 | 0.205261 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534648 | atatcaacacacaca[C/G]ccccaaagagataca | 5522 |
rs4689476 | snp | A/G | 0.0973687 | 0.197999 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534857 | TCAGTGTGAGCCTCA[A/G]GAGTCACTGTCCGCT | 5522 |
rs4689477 | snp | A/C | 0.44768 | 0.153045 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6540022 | GCTCCAATGACACCA[A/C]GCTTCTCACTTTAAA | 5522 |
rs4689478 | snp | A/G | 0.243347 | 0.249911 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6549413 | CCGGGGAGGCCTCCC[A/G]GAGGAGGTGACTTTT | 5522 |
rs4689479 | snp | A/G | 0.152001 | 0.229992 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6550060 | AGCTGAGGTCACAGC[A/G]GGGTAGGGGGACAGC | 5522 |
rs4689480 | snp | C/T | 0.499087 | 0.0213463 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6550232 | CCTCCAAGCTTCCTG[C/T]TCCCCTCCTCACAGC | 5522 |
rs4689481 | snp | A/G | 0.375 | 0.216506 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6554938 | gaaggaaggaaagaa[A/G]gaaagaaagaaagaa | 5522 |
rs4689482 | snp | A/G | 0.0364509 | 0.129988 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6557648 | tgctgtgTAGTGAGC[A/G]CTGTGGAGATGGGCA | 5522 |
rs4997044 | snp | A/G | 0.393619 | 0.204631 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389948 | ATGGGGTCAGAGATG[A/G]GAGGCTGAGGAGTTG | 5522 |
rs4997045 | snp | C/G | 0.172674 | 0.237741 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6389690 | TACACCTTCTGGGCA[C/G]TTCCTGGGAGCCAGG | 5522 |
rs5019274 | snp | C/T | 0.471578 | 0.115772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399133 | acaggaaacgttttg[C/T]gggtgaaggccatgc | 5522 |
rs5022597 | snp | A/T | 0.482083 | 0.0929373 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6483157 | GATTGATTGATTGAT[A/T]GATAGACGATAGATA | 5522 |
rs5022598 | snp | A/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6483145 | gatagatagatagat[A/T]gattgattgatagat | 5522 |
rs5027682 | snp | G/T | 0.270621 | 0.249148 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6514044 | CATGGTTCTGCTTTT[G/T]TATTCTTCAGCTTCC | 5522 |
rs5855908 | in-del | -/G | 0.15665 | 0.231917 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329608 | CCTGCTCATCTTATC[-/G]GGGGGCCCACGACCA | 5522 |
rs5855909 | in-del | -/GTCTG/TCTGG | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374034 | GTTGGTGTTAGTGTG[-/GTCTG/TCTGG]ACTCCTCCAAGGCAT | 5522 |
rs5855910 | in-del | -/T | 0.362104 | 0.223456 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6379032 | GCCTGACGCCAAGGC[-/T]TGAGGCTCTGGCCAC | 5522 |
rs5855911 | in-del | -/CTT | 0.466618 | 0.124806 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402498 | TTTTCCTTCTCCTTC[-/CTT]CTTTCCTTCTTGCCT | 5522 |
rs5855912 | in-del | -/A | 0.0737376 | 0.17729 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436905 | GAGGTCCAAATGCCC[-/A]AGTTGTCTTTGACTA | 5522 |
rs5855913 | in-del | -/A | 0.424037 | 0.179474 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6446879 | AAAGTGTCTGCTTGT[-/A]AAAAAAAAAAAAACA | 5522 |
rs5855914 | in-del | -/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6450228 | TCTATGGGGTGGAGT[-/G]GGGGGGTTCAGCACC | 5522 |
rs5855915 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456308 | TGAAGGATGTTATTT[-/C]CCCCCCCCCCCTTTA | 5522 |
rs5855916 | in-del | -/GGT | 0.475259 | 0.108435 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458716 | GCAGGTGCTGAGCTG[-/GGT]GCAGGGTGCAGCGGA | 5522 |
rs5855917 | in-del | -/GGT/GTG | 0.5 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458717 | CAGGTGCTGAGCTGG[-/GGT/GTG]CAGGGTGCAGCGGAA | 5522 |
rs5855918 | in-del | -/AA | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477752 | AAAAAAAAAAAAAAA[-/AA]CTGGAACTGGACCTC | 5522 |
rs5855919 | in-del | -/AT/TA | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6482993 | TATCTATTAATAAGA[-/AT/TA]ATATGACTTTAGCCT | 5522 |
rs5855920 | in-del | -/TT | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6483148 | AGATAGATAGATTGA[-/TT]GATTGATAGATAGAC | 5522 |
rs5855922 | in-del | -/G | 0.499673 | 0.0127754 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6519913 | GCAGTCAGGTAACCA[-/G]GAAGTCCTGGCTTGC | 5522 |
rs6148287 | in-del | -/ATGTGTAGATACATGCC | 0.0584853 | 0.160693 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429081 | AGGCATCCACAGACA[-/ATGTGTAGATACATGCC]ATGTGTAGATACATG | 5522 |
rs6148288 | in-del | -/CCATGTGTAGATACATG | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429096 | ATGTGTAGATACATG[-/CCATGTGTAGATACATG]GGCATGACTCTGTTC | 5522 |
rs6414629 | snp | C/T | 0.319856 | 0.240042 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403371 | TTCCTCCTCGCTTCC[C/T]GCCCCCTAGGTGTTT | 5522 |
rs6446489 | snp | C/T | 0.418169 | 0.184985 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321738 | TGCCAAACTACGTGG[C/T]TCTGCTGCAAGTCCA | 5522 |
rs6446490 | snp | A/G | 0.492137 | 0.0622048 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322920 | TCCCTGCAACAGGAC[A/G]CACTGGAGTGAAAAA | 5522 |
rs6446491 | snp | C/G | 0.474544 | 0.10991 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6326627 | AAGGCATCACACATG[C/G]TCTCATCCCCAAAGC | 5522 |
rs6446492 | snp | A/G | 0.316243 | 0.241064 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6326780 | CTGCCTCTCCACAGC[A/G]CGCTGCCCATCTGCG | 5522 |
rs6446493 | snp | C/G | 0.178144 | 0.239451 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6364192 | AGACTGGTCAAGGAA[C/G]GCCTCTTTAAGAAGG | 5522 |
rs6446494 | snp | A/G | 0.314301 | 0.241589 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374341 | AAACCAGAGCTCAAA[A/G]CCAGTTTTTTAGTAA | 5522 |
rs6446495 | snp | C/T | 0.313326 | 0.241847 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374546 | TTGTCATCTGGCCTG[C/T]GCAGAAAGGCTTTAC | 5522 |
rs6446496 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6377909 | ATTAAGAGGCCGGCC[A/G]GGGTCCTAAACCAAG | 5522 |
rs6446497 | snp | A/T | | | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382675 | ctctctctctctctc[A/T]cacacacacacacac | 5522 |
rs6446498 | snp | C/T | 0.449473 | 0.150701 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6398953 | gcaaccagggggaag[C/T]tcaaaatacccacac | 5522 |
rs6446499 | snp | C/T | 0.432063 | 0.171327 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6400590 | ATTGGGTGATTTGGG[C/T]GTTTGATCTACTAAG | 5522 |
rs6446500 | snp | A/G | 0.368733 | 0.220005 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402430 | TCAGTGTTCTCACCT[A/G]CAAAATGGGCATGGT | 5522 |
rs6446501 | snp | A/C | 0.324855 | 0.23853 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403047 | AGGCGGCAGGAGGGC[A/C]GTAATTTCCACTGAG | 5522 |
rs6446502 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6431560 | GGCTAAGTCCAAAGC[C/T]GTGGAGGGGACATGG | 5522 |
rs6446503 | snp | C/G | 0.0829062 | 0.185956 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432387 | GCCCCAGGGATGAAA[C/G]AAGTGTTGTACCCAC | 5522 |
rs6446504 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433614 | CCCATTGGGCCAATA[A/G]GCATACGGGTTCCAA | 5522 |
rs6446505 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6435470 | ATTATGTACAGTTGA[C/T]ATTTTCATCTGATTT | 5522 |
rs6446506 | snp | C/T | 0.175254 | 0.238565 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437498 | AGAGGAAGTTAGGGA[C/T]AGAGCTCTTATCAAA | 5522 |
rs6446507 | snp | A/G | 0.103438 | 0.202533 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6465592 | gtgctaagatacaaa[A/G]ccttttcatgccttc | 5522 |
rs6446511 | snp | C/T | 0.477853 | 0.102875 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534749 | GCAGTGACAACCCCG[C/T]CTCCGCATGGCTGCC | 5522 |
rs6811173 | snp | A/C | 0.409041 | 0.192888 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422977 | ATTCTACATGCACCA[A/C]CCCAATCCAGGGTAC | 5522 |
rs6811801 | snp | C/T | 0.0792906 | 0.182643 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329220 | GCAGGGCAGAAACCC[C/T]CCCTACGGTGAGGTG | 5522 |
rs6811846 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432071 | CCTCTTAACGCATCA[C/T]CTTAAGGCTTAATTT | 5522 |
rs6812254 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372115 | GGCCCCAGTGCTGGT[C/T]CTCCTATGCTAACAC | 5522 |
rs6812256 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372118 | CCCAGTGCTGGTCCT[C/T]CTATGCTAACACAGC | 5522 |
rs6812869 | snp | G/T | 0.435407 | 0.167703 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6440449 | TCACAGGGCAGGTGT[G/T]GGGGGCTCTTAGCAA | 5522 |
rs6813305 | snp | A/G | 0.253544 | 0.249975 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455144 | TGACTCCAGAGCTGC[A/G]TTGCATTCGTGGACT | 5522 |
rs6813643 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387892 | TTCATCTCAGAACAA[G/T]CCCATCGACCAATTA | 5522 |
rs6813669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520803 | CAGTCTTCCCTGCAT[C/T]GGGTCACAGATTCTT | 5522 |
rs6813943 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360418 | TCCATGAGAAAGAGG[A/G]CTGCAGCCTTGGGCT | 5522 |
rs6813956 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6441204 | GGAAAAAAGCACCTC[A/G]GGGCCCTCATGCATG | 5522 |
rs6814782 | snp | G/T | 0.43309 | 0.17023 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455885 | GCTGCCCACAGCCTT[G/T]CATCTCTGACCACCT | 5522 |
rs6815530 | snp | A/G | 0.451359 | 0.148171 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411820 | GCCTCCCAAAGTGCT[A/G]GGATTATAGGCATGA | 5522 |
rs6817302 | snp | A/G | 0.195526 | 0.243993 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6345300 | CCTGAGTGAATGGGC[A/G]GGAGGCGTAGGTGGG | 5522 |
rs6817323 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520951 | TTGTCCATTGTTCTT[A/G]TTAATTATCACCATG | 5522 |
rs6817472 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6345336 | AGTGTCCtgtagtag[A/G]cggtggaacggcccc | 5522 |
rs6817820 | snp | A/T | 0.444444 | 0.157135 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6518923 | gcaagactctgtctt[A/T]aaaaaaaaaaaaaaa | 5522 |
rs6818027 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6488750 | tttgctaaggatgct[C/T]gcagaaattatcaat | 5522 |
rs6819692 | snp | G/T | 0.480382 | 0.097079 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455993 | CCAGAAATCCTGGGG[G/T]GGGGGAGCTGCGCCC | 5522 |
rs6820050 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373579 | tctccatctctctag[C/T]gctcagtccaaggcc | 5522 |
rs6820874 | snp | A/G | 0.277334 | 0.248501 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6516726 | TCTACATGCTTTGGC[A/G]TTAACACATTTCATA | 5522 |
rs6821118 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6516847 | GTGGGAGATGTCACT[C/G]GTTCATGAAACCCCG | 5522 |
rs6821739 | snp | A/C/G | 0.0055829 | 0.0525657 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456317 | TTATTTCCCCCCCCC[A/C/G]CCTTTATTCTACTGT | 5522 |
rs6822123 | snp | A/G | 0.427423 | 0.176128 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6349099 | CATGCAAGGACTGGC[A/G]CCCCCGAGCTTCTCT | 5522 |
rs6823629 | snp | A/C | 0.114738 | 0.210248 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6377460 | CAGGAGTTCGAGATC[A/C]ACCTGGCCAACATGT | 5522 |
rs6824477 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374154 | TCCCTGGACTCTCAG[G/T]AGAGAGAGGGAGCCC | 5522 |
rs6825304 | snp | A/G | 0.369142 | 0.219784 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404695 | CAGATTCCAAGGGGG[A/G]TTCTAAGGAGGCAGG | 5522 |
rs6825398 | snp | A/C | 0.111224 | 0.207945 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6543227 | CAGCCACAGCTGTCA[A/C]TGGACTACAACTCGG | 5522 |
rs6826043 | snp | C/T | 0.312348 | 0.242101 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374245 | CCTCCTGCTTCCTTC[C/T]GGCAACATTGCTTTC | 5522 |
rs6826490 | snp | A/G | 0.105569 | 0.204058 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429386 | CAGGCCCTCGTACCT[A/G]GTAGGAAGACAGTAA | 5522 |
rs6826531 | snp | C/G | 0.496874 | 0.0394129 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404540 | CCAGGTAGCACGCTT[C/G]TCACTCTAAAGGTTT | 5522 |
rs6826908 | snp | A/G | 0.184203 | 0.241186 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429536 | CAACAGTATGGGTTG[A/G]GGATGATCTCAGAGA | 5522 |
rs6827050 | snp | G/T | 0.16911 | 0.236552 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6348983 | GTGGCCCAGGTGTGA[G/T]TGGTAAGGCTGGATT | 5522 |
rs6828090 | snp | C/G | 0.429538 | 0.173972 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6457755 | acattgagatgtcaa[C/G]tgctttatttctttg | 5522 |
rs6828471 | snp | A/G | 0.00417917 | 0.0455205 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329227 | AGAAACCCTCCCTAC[A/G]GTGAGGTGAGGTGCG | 5522 |
rs6828643 | snp | C/T | 0.396182 | 0.202807 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407487 | tgcaacctcgcctgc[C/T]gggttcaagcgattc | 5522 |
rs6828983 | snp | A/C | 0.499859 | 0.0083854 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334735 | TGGAAATACCTAAAC[A/C]TATGACAACCTGTCC | 5522 |
rs6829169 | snp | A/G | 0.480144 | 0.097642 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6440240 | ATACATGTTGGATGC[A/G]TGCGCAGATGGACAG | 5522 |
rs6829192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6440273 | GAGTACATGTTGCAT[A/G]AATTCATTTTCTATT | 5522 |
rs6829585 | snp | C/T | 0.480853 | 0.0959518 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6457735 | tgtaatttaaagcat[C/T]agaaacattgagatg | 5522 |
rs6829610 | snp | C/T | 0.207253 | 0.246318 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329079 | GAATTTCATGTCCTG[C/T]CCCTTGAATCTGAGC | 5522 |
rs6829828 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6440563 | GCTGGCTCCGTAAAC[C/G]CCAGCAGGCTGGTCT | 5522 |
rs6829844 | snp | C/G | 0.14926 | 0.228804 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329211 | CAGACCCCTGCAGGG[C/G]AGAAACCCTCCCTAC | 5522 |
rs6829846 | snp | C/T | 0.0594255 | 0.161807 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6329217 | CCTGCAGGGCAGAAA[C/T]CCTCCCTACGGTGAG | 5522 |
rs6830207 | snp | G/T | 0.356811 | 0.226034 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410621 | GCTGGCTGGTCTGCA[G/T]GTGTGTGAGGGGGTG | 5522 |
rs6830667 | snp | C/T | 0.496616 | 0.0409947 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6337467 | GAACTAGGCTTTCTG[C/T]CACTTGGAGGTGAGG | 5522 |
rs6831294 | snp | C/T | 0.472803 | 0.113397 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6440556 | GTAACATGCTGGCTC[C/T]GTAAACGCCAGCAGG | 5522 |
rs6831971 | snp | C/T | 0.383246 | 0.211531 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6365740 | CCCCTCCAGCCCACC[C/T]GGCCGTGCGGACCTG | 5522 |
rs6831981 | snp | A/G | 0.414741 | 0.188044 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6396042 | CTGGGTCACCGGGGA[A/G]CTCACACAGGAGCAT | 5522 |
rs6831994 | snp | C/T | 0.411914 | 0.190483 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6395856 | CAGCTGCAGGCCTTG[C/T]TCCCCAGCTGGTGTG | 5522 |
rs6832910 | snp | G/T | 0.330016 | 0.236849 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6538372 | GCCCATCTGCCAAGT[G/T]CCACCGACACACAGG | 5522 |
rs6833187 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463861 | CTGCTGAACCCTCTC[A/G]ATTGCCTTTCATCGC | 5522 |
rs6835336 | snp | C/T | 0.405255 | 0.195948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6378265 | CACTCATGGGATTTA[C/T]ATGCTGCTCAAAAAG | 5522 |
rs6836145 | snp | A/C | 0.434109 | 0.169127 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6451335 | GTAGCCCAGGCTTCT[A/C]GGCACGGCCCACAGC | 5522 |
rs6836154 | snp | C/G | 0.364193 | 0.222396 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6451340 | CCAGGCTTCTCGGCA[C/G]GGCCCACAGCTTGCA | 5522 |
rs6836802 | snp | A/G | 0.126219 | 0.217206 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388624 | AATGAAGGGCAggac[A/G]ggcatggtggctcac | 5522 |
rs6837213 | snp | G/T | 0.487432 | 0.0782705 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6331051 | AGGGTACTGGCTCAG[G/T]ATGTGTAACAACTAA | 5522 |
rs6837903 | snp | A/G | 0.119281 | 0.213102 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372462 | AATCAAACCAAACCC[A/G]CCACCCAACGGAAGC | 5522 |
rs6838132 | snp | A/G | 0.3742 | 0.216966 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402699 | GCGATGGAGGGAGAC[A/G]TGGGGATTCTGAGGG | 5522 |
rs6838955 | snp | C/T | 0.310632 | 0.242536 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411843 | AGGCATGAGCCACCG[C/T]GCCCGGCCTCCACCC | 5522 |
rs6839124 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406706 | aggctgcagtgagcc[A/G]agatcgcaccactgc | 5522 |
rs6839498 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6341208 | gtcgggtgtggtggc[C/G]ggcacctgcaatccc | 5522 |
rs6842035 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432122 | AACCAGACCTTCAGA[C/T]GACAGCAGTAGGCTT | 5522 |
rs6844822 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437148 | ACTCTCAGCGTCATG[A/G]TGCACTGTGTCTTGC | 5522 |
rs6845693 | snp | C/G | | | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382642 | TCTCTCTCTCTCTCT[C/G]TCTCTCTCTCTCTCT | 5522 |
rs6845713 | snp | A/G | 0.208474 | 0.246527 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373901 | CGTGTATGTGCATGC[A/G]TGTGTGTGTGTGTGT | 5522 |
rs6845887 | snp | C/T | 0.0441095 | 0.141807 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382756 | gccttcacagcatat[C/T]gggatgccagccact | 5522 |
rs6846152 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6349261 | TCAGGTGCATGTGAG[A/C]Cctggagttggaagg | 5522 |
rs6847241 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437656 | ACTCACGAATATGCT[C/G]AGGGACTCAGTGCAC | 5522 |
rs6847568 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6327787 | TTTAGTGGCCCCCTG[C/T]GATCACCATGCCAGC | 5522 |
rs6848000 | snp | G/T | 0.481009 | 0.0955756 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6337655 | GCCAGAATCACAGGG[G/T]GCACCGGTGCTGGGT | 5522 |
rs6849513 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461096 | TGATCCACCTGGGCA[C/T]CACCTATTTGGCTTT | 5522 |
rs6849568 | snp | A/G | 0.481932 | 0.0933148 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382947 | ACAGAGTGTTCTAAA[A/G]GCAGCCCCCACCTGC | 5522 |
rs6849702 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6543547 | ccaacctggccaaac[C/T]ccgtctctactaaaa | 5522 |
rs6849998 | snp | C/T | 0.102726 | 0.202016 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6395659 | GTGGTATGCCAAGGG[C/T]GCAGACCCGCCAGTC | 5522 |
rs6850064 | snp | A/G | 0.411746 | 0.190626 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6538426 | CCCAGCGACGCAAGC[A/G]TTTCAGAGCAAAACG | 5522 |
rs6850236 | snp | C/T | 0.40386 | 0.197046 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6498730 | ACCCACTGAGCCCAG[C/T]GAGCTCCCGGGCTGT | 5522 |
rs6851179 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6346570 | GGGCCTCTGCTGCAC[A/G]CCCATGCCAGGAATA | 5522 |
rs6851340 | snp | C/T | 0.421526 | 0.181876 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383096 | TGCAGAACGGCAATT[C/T]GACAAGCCGCAAACA | 5522 |
rs6851735 | snp | C/T | 0.140919 | 0.224948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361027 | TTATTTTAACTTAAT[C/T]ACCCCTTTAAGGCCC | 5522 |
rs6852624 | snp | C/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6443850 | GTGCATCTTTTCTGG[C/G]TGTCTCAGCCCACAC | 5522 |
rs6852862 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421812 | CAGTTACCCTGTTGG[C/T]AACAGAATGAAATAA | 5522 |
rs6853134 | snp | A/G | 0.358515 | 0.225221 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408722 | TCCCTGAGCACTTGG[A/G]CCACAGGTGATCTGC | 5522 |
rs6853144 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6377948 | CACTGCCCCGCAAGG[C/T]CGCGGTGACAGCCCC | 5522 |
rs6853582 | snp | C/T | 0.391024 | 0.206427 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408227 | GTGCCAACAAAATGG[C/T]AGAAGAGACCTAGAC | 5522 |
rs6853747 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334557 | CTCATTTCTGCTGGT[A/G]TCTGTCTCACTGGTA | 5522 |
rs6854172 | snp | C/T | 0.375 | 0.216506 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408561 | GTAAACTGAGGCCAC[C/T]CTGGAGCACAGATAA | 5522 |
rs6855700 | snp | C/T | 0.27008 | 0.249192 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6366024 | GGTTGCTTAAACAGA[C/T]GTTGAAACTGCACCG | 5522 |
rs6856061 | snp | C/T | 0.317933 | 0.240593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6346464 | CTGTACCTGACTTTG[C/T]GGGTGTTGGTGCCAT | 5522 |
rs6856207 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434363 | ttttttcttttcttt[C/T]ttttttttttttgga | 5522 |
rs6856476 | snp | A/G | 0.18325 | 0.240924 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444196 | CCTAACATGGCTAGA[A/G]GCAGTGGCCCCGAAA | 5522 |
rs6857081 | snp | C/T | 0.430583 | 0.172886 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404684 | GCTGTAGTTAACAGA[C/T]TCCAAGGGGGGTTCT | 5522 |
rs6857676 | snp | A/C | 0.0622301 | 0.165053 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375021 | AGGGACATAAACAGG[A/C]TTTTTATGAAGGCCA | 5522 |
rs6858145 | snp | A/T | 0.481473 | 0.0944461 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6435464 | CAAGGCATTATGTAC[A/T]GTTGATATTTTCATC | 5522 |
rs6858396 | snp | A/C | 0.250732 | 0.249999 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384193 | GCCAGAACCACCCAG[A/C]CCAGCTGTGCTAGGG | 5522 |
rs6858815 | snp | A/G | 0.040671 | 0.13668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432065 | GCCCCACCTCTTAAC[A/G]CATCACCTTAAGGCT | 5522 |
rs7340834 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6438552 | AGATAAGATTGTATA[A/G]TGGTTGGAATGTTTC | 5522 |
rs7340835 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6438634 | CTTAATATTTTTATG[A/G]GTGTCTGGTGACACA | 5522 |
rs7375187 | snp | A/T | 0.481627 | 0.0940692 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6457369 | ccatagggaatgcac[A/T]gggaatttttttttc | 5522 |
rs7375807 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512485 | gtggtagtggtggtg[A/G]tggtgatggtggtgg | 5522 |
rs7375817 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512530 | gtggtggtggtggtg[A/G]tggtgatggtggtga | 5522 |
rs7375819 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512536 | gtggtggtgatggtg[A/G]tggtggtgatggtgg | 5522 |
rs7376591 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6466240 | acagactcgcctgcc[A/G]cacgtacccctctgc | 5522 |
rs7376777 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454485 | GAGACTGCACGCTGG[A/G]GAGGGGAGCCCCGCC | 5522 |
rs7377185 | snp | C/T | 0.458775 | 0.137524 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406074 | AGCATTTATTAAGTG[C/T]TCATGTTGAGCCTCA | 5522 |
rs7377342 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512521 | gtgatgttggtggtg[A/G]tggtggtgatggtga | 5522 |
rs7377343 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512539 | gtggtgatggtgatg[A/G]tggtgatggtggtga | 5522 |
rs7378300 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454451 | AAGCCAGCTGCCATC[A/G]AAGGAGTCCAACTGC | 5522 |
rs7378410 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454554 | GACCATCTCAGTCCC[C/T]CCAGATCAGTCCACC | 5522 |
rs7434469 | snp | C/T | 0.489083 | 0.0730708 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409019 | GGAGATGTAGGCAAA[C/T]AGCTAGAGTGAAAGC | 5522 |
rs7434644 | snp | A/G | 0.266819 | 0.249434 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363376 | gaggtcaggagatcg[A/G]gaccatcctggctaa | 5522 |
rs7434646 | snp | C/T | 0.367913 | 0.220446 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402243 | TACACAGGAAGGCTG[C/T]GCACCCACACCCATC | 5522 |
rs7435050 | snp | A/C | 0.224412 | 0.248687 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358585 | ggagaaaatttttgc[A/C]atctactcatctgag | 5522 |
rs7435090 | snp | A/G | 0.157972 | 0.232445 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358665 | aaaaaatcaaacaac[A/G]ccatcaaaaagtggg | 5522 |
rs7435598 | snp | C/T | 0.198944 | 0.244731 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6533818 | ACAGGCCCGTCGACC[C/T]GGGTGGCCGTTACAT | 5522 |
rs7435711 | snp | C/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403623 | AAAAATACAACCtgg[C/G]aggacgaggcagggg | 5522 |
rs7437390 | snp | A/G/T | 0.0240944 | 0.107291 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407280 | CAAGTGTGAGGCAAG[A/G/T]GGGGGAAGTCAACAA | 5522 |
rs7437424 | snp | C/G/T | 0.0170452 | 0.0908952 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407394 | AGAAACCCAACTGGt[C/G/T]tttttgtttgtttgt | 5522 |
rs7437478 | snp | C/T | 0.431769 | 0.17164 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6400283 | CATCATCTATTAAGC[C/T]AGAGATTAAAGAGAT | 5522 |
rs7437711 | snp | A/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6438429 | CTTAGCTCAGTTTGG[A/T]AGAGTTTGGTGGACG | 5522 |
rs7437830 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408743 | GGTGATCTGCGGGGC[A/G]CCCTGAGAAACTCCA | 5522 |
rs7438559 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6401005 | CGTTCCCACACACGT[C/T]GGTCAAGTGGCACGT | 5522 |
rs7439007 | snp | A/G | 0.474272 | 0.110462 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409692 | CTGCCACCCCCCCAT[A/G]TCCCAGCCCTGGAGA | 5522 |
rs7439469 | snp | A/G | 0.309154 | 0.242901 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367517 | TGACAGCCAGAATCC[A/G]CCCCACTGAGACTTG | 5522 |
rs7440484 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407097 | aggctacagagggaa[C/T]gtaggcctacggaca | 5522 |
rs7440689 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6483113 | gactgatagataaat[A/G]gatagatagatagat | 5522 |
rs7441490 | snp | A/G | 0.499997 | 0.00119808 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6343311 | GCTAAAAACTGCTGC[A/G]CAATCTTTTTGCTGG | 5522 |
rs7441503 | snp | A/G | 0.431029 | 0.17242 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6401021 | GGTCAAGTGGCACGT[A/G]GCAGGACATGGAAAC | 5522 |
rs7441682 | snp | G/T | 0.450231 | 0.149691 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361769 | GACAGAGCTGGGATG[G/T]GCACCCAGGCAGCTG | 5522 |
rs7653967 | snp | C/T | 0.431769 | 0.17164 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399602 | TCACTCTCCCAGGTG[C/T]ACACAGCTTCCAGGG | 5522 |
rs7654138 | snp | A/C/T | 0.030665 | 0.119967 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6326794 | CACGCTGCCCATCTG[A/C/T]GTTCTGCCGGTGCTA | 5522 |
rs7654321 | snp | A/G | 0.336245 | 0.234652 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6497310 | ACAATACTTAAGGCC[A/G]TGTGATATTGGTGCA | 5522 |
rs7655230 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6527164 | TGAAATATTTCCATT[C/T]CTGCCTAGAATTCCA | 5522 |
rs7655407 | snp | A/G | 0.379158 | 0.214052 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402804 | ACACTGCTAGTGGGA[A/G]GCATTCAGGTGAGAG | 5522 |
rs7657189 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388207 | GGAGAGGCACACAGG[A/G]GCCACTGAACAAGGA | 5522 |
rs7657197 | snp | A/G | 0.284209 | 0.247648 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388215 | ACACAGGAGCCACTG[A/G]ACAAGGAGGCCTCAG | 5522 |
rs7657246 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6347126 | TCTGCCACGATTGAA[G/T]TTGGGTGACCTTGGG | 5522 |
rs7657377 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6435022 | cagccactcactgta[C/T]ttcctttcagtccat | 5522 |
rs7657577 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388377 | CGtgggttgaactgc[A/G]tcccacaaaaagatg | 5522 |
rs7658189 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415026 | AAGGGATGGTGTCAG[G/T]AACAGGTGCGGATAT | 5522 |
rs7658616 | snp | A/G | 0.44768 | 0.153045 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415301 | GTCAGACCACCGGCC[A/G]TTTCAATCCATTTGC | 5522 |
rs7660104 | snp | G/T | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6511090 | tagctgtccctgaat[G/T]tgtccttctcttaat | 5522 |
rs7661778 | snp | C/T | 0.417196 | 0.185864 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402987 | GTGCTAGGCTCTGCA[C/T]GTCTCCCGGCTCACT | 5522 |
rs7662145 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403820 | gtgtgcagagattgc[A/G]ccgctgcactccagc | 5522 |
rs7663148 | snp | A/T | 0.430434 | 0.173042 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6351331 | AATAAATAAATAAAT[A/T]AATTAATTAATTAAT | 5522 |
rs7663181 | snp | C/T | 0.120326 | 0.21374 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6351381 | TTAGGTCTGTAGCCC[C/T]GTGGCAAACACACCC | 5522 |
rs7664616 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406287 | GACCAGCACCTTCCA[C/T]GGGGAAGTTGGTCTT | 5522 |
rs7664714 | snp | C/T | 0.495483 | 0.0473088 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464064 | CTGTCCCTTACAAAC[C/T]ATGTGACATTGAACA | 5522 |
rs7664936 | snp | A/T | 0.499121 | 0.020948 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464151 | CAGGTCTGGGGCATC[A/T]CCAATGAGATGCACG | 5522 |
rs7664961 | snp | C/T | 0.429837 | 0.173662 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464201 | TAGTATTATAGTACA[C/T]AGCCAATAAATGGTG | 5522 |
rs7665893 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6328727 | GACGGCTGGACTTGT[A/G]GATTGTGACAAGCCC | 5522 |
rs7668629 | snp | A/C | 0.465578 | 0.126594 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6562869 | GCATAAAAGCCAACC[A/C]GGGTCACTTCCCAGG | 5522 |
rs7669196 | snp | A/G | 0.421684 | 0.181726 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399061 | cctacagtgaccaaa[A/G]gcaaatcactggcta | 5522 |
rs7671158 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6510744 | gcactttgggaggcc[A/G]aggtgggcggacccc | 5522 |
rs7671165 | snp | C/T | 0.431916 | 0.171483 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399375 | ATTTAATCCCCTCAA[C/T]GTAATCGAGTCCACC | 5522 |
rs7671264 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508538 | agcttgcagtgagcc[A/G]agatcgtgccactgc | 5522 |
rs7671369 | snp | C/T | 0.431769 | 0.17164 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399471 | CAATCCACAAGTTCA[C/T]CCATCCAGATTTGTC | 5522 |
rs7673505 | snp | A/T | 0.0970103 | 0.197722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6401345 | CGAGTATTGTCAGGA[A/T]CCGTCTTTGGACTGC | 5522 |
rs7675249 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6435163 | cttatctgtcctctg[C/T]atcatgttctaatat | 5522 |
rs7675289 | snp | C/T | 0.386504 | 0.209444 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6443089 | TCCACCCCAGGAACC[C/T]GGGAGAACCAAGCTC | 5522 |
rs7675723 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454234 | GGAGGGCCAGAGCAC[A/G]GTCTCCTATCCCATC | 5522 |
rs7675854 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375315 | ACTGGATGCTGGGCA[C/T]GTGTGTGTCTGTTTC | 5522 |
rs7675952 | snp | C/T | 0.380919 | 0.21298 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493242 | ACACACGCACGCGCG[C/T]GCACATACACACACC | 5522 |
rs7676183 | snp | C/T | 0.496416 | 0.0421803 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6523436 | ggcagtggccttgga[C/T]acatacatttcaccg | 5522 |
rs7676217 | snp | A/G | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6510953 | ctgcactccagcctc[A/G]gcaacagagtgagac | 5522 |
rs7676409 | snp | A/C | 0.497473 | 0.0354532 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6340632 | cggccactcactctg[A/C]gcaccagcgtctctc | 5522 |
rs7676415 | snp | C/T | 0.285519 | 0.247464 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6523605 | gacgcgggacctgca[C/T]acactgctgggggca | 5522 |
rs7676737 | snp | C/T | 0.496483 | 0.0417852 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6523764 | atgaacactggaacg[C/T]gaatgttcccagcag | 5522 |
rs7676746 | snp | C/G | 0.138886 | 0.22395 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6511243 | ttagtcgttCCGCtg[C/G]tgatgctgatgctga | 5522 |
rs7677883 | snp | A/C | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6511120 | tttcttcatctgtaa[A/C]atggagataataatc | 5522 |
rs7678084 | snp | C/T | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6511233 | tcagtacatgttagt[C/T]gttCCGCtggtgatg | 5522 |
rs7678282 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323149 | GCTGGGGCAGGGAGG[C/G]GGCCCAAACTTCCTG | 5522 |
rs7678340 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388190 | TAGGGCAACCCCCAA[A/G]TGGAGAGGCACACAG | 5522 |
rs7678531 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388260 | CTGGGCACAGCACAG[A/G]CCTACCAATGGGTGC | 5522 |
rs7679988 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6351665 | ATCACCCTGCAGAAG[A/G]AGAAAAATCACTGTC | 5522 |
rs7680478 | snp | A/G | 0.451608 | 0.147832 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6558959 | ACCACCCAGCCCTGC[A/G]GCTCTGATGGGACAC | 5522 |
rs7680695 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6388656 | cctgtaatcccagca[C/T]tttggggggccgagc | 5522 |
rs7682727 | snp | A/G | 0.268452 | 0.249318 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332772 | AGCACGTGGCACCCC[A/G]TGTGTGAGGAGTGAC | 5522 |
rs7686677 | snp | G/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6485036 | catttagcctgtagg[G/T]ttttctcatagatgc | 5522 |
rs7688267 | snp | A/G | 0.487809 | 0.0771174 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6525635 | cctttcgaaagcctt[A/G]ccctactgctgattc | 5522 |
rs7691387 | snp | A/G | 0.308166 | 0.243139 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6453822 | AAGCACAGCCCCACC[A/G]AGGGCCACGTTGGCT | 5522 |
rs7691957 | snp | A/C | 0.40157 | 0.198813 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6528945 | CTCAGCCGGCCTGCA[A/C]CCAGGTGATTAAAAG | 5522 |
rs7692151 | snp | C/G | 0.209997 | 0.246779 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6478334 | tcccttttaatatta[C/G]gtgtagtcatgagac | 5522 |
rs7692662 | snp | C/T | 0.48435 | 0.0870631 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6491784 | CTCTCCTGCTGGCCA[C/T]GTGAATATGTGCCTA | 5522 |
rs7693590 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508481 | gtaatcccagctact[C/T]gggaggctgaggcaa | 5522 |
rs7694129 | snp | C/T | 0.243347 | 0.249911 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383585 | AATTCTGCCCCACTG[C/T]TGCCTTCCCGTGAGC | 5522 |
rs7696308 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6454103 | GTTCTTCCTGTGACT[A/G]TTCAGGGGGACAAGA | 5522 |
rs7696443 | snp | C/G | 0.137867 | 0.223442 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6371601 | GGTTAGAAGCGGGGA[C/G]TCTGGGGCCTGAGGG | 5522 |
rs7696558 | snp | A/G | 0.421684 | 0.181726 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322014 | GTCCTGGGGAGGGCC[A/G]CACTCCTGAAGCCAC | 5522 |
rs7696589 | snp | A/G | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6510909 | tggaacccgggaggc[A/G]aaggttgcagtgagc | 5522 |
rs7696856 | snp | G/T | 0.0614824 | 0.164198 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6529013 | CACACGGACGCGCAC[G/T]AAACTTACTTTATTT | 5522 |
rs7697730 | snp | A/G | 0.434831 | 0.168337 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322519 | CAGGGAGGGCTGCAG[A/G]GGGTAAGTCAACTGC | 5522 |
rs7699546 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375273 | TCAGGAAGAGCACTG[A/G]CTACTGCTTTATATT | 5522 |
rs7699696 | snp | C/T | 0.431769 | 0.17164 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399316 | AGAGGGGAGAGGAAG[C/T]GCCAGCAGCCACCTG | 5522 |
rs9291114 | snp | A/G | 0.447162 | 0.153712 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6405738 | CATCACGAAAACCTC[A/G]TTTGCAAACCCAAAT | 5522 |
rs9291115 | snp | C/T | 0.425123 | 0.178415 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411697 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACACC | 5522 |
rs9291116 | snp | A/G | 0.414576 | 0.188188 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411844 | GGCATGAGCCACCGC[A/G]CCCGGCCTCCACCCT | 5522 |
rs9291117 | snp | A/G | 0.202343 | 0.245416 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6445880 | TCTGCCCACAGTGTC[A/G]CAGAACATAACACAG | 5522 |
rs9654056 | snp | A/G | 0.291493 | 0.246533 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6544706 | TCGGGCAGAAAAGGA[A/G]GAAGCATAAGCAAGA | 5522 |
rs9654057 | snp | C/G | 0.20511 | 0.245937 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6544886 | GTGAGGTTGATTCCA[C/G]GTTTATTTTGTGTTG | 5522 |
rs9968250 | snp | A/G | 0.188 | 0.24219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6445529 | AGACAGACAGATGAG[A/G]TTGCAAAGTTGAAGC | 5522 |
rs9968308 | snp | A/T | 0.232651 | 0.249397 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6448027 | GCAGAGGCTCCTGGT[A/T]CACCCCCGTGGGAGC | 5522 |
rs9985765 | snp | C/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6495008 | CACGCAGCGAGGTTG[C/G]TGGAGGAAGAGCAAC | 5522 |
rs9991896 | snp | G/T | 0.420574 | 0.182769 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6442455 | TGGGGCCACCAAGCC[G/T]TGACTGTGGTGGTCG | 5522 |
rs9992005 | snp | C/G | 0.403684 | 0.197183 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412495 | AGATGCCAGCTGTGT[C/G]CTTGAATAAAAAATG | 5522 |
rs9992071 | snp | A/G | 0.337841 | 0.23406 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6500563 | ATTTGGAAGGGGCCC[A/G]TCACAGGGGACCCCC | 5522 |
rs9992280 | snp | A/G | 0.444666 | 0.15686 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412734 | CAAATTCATATGTTG[A/G]AACCCTAACCCCAAG | 5522 |
rs9992880 | snp | A/T | 0.110872 | 0.20771 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6515640 | AAATTTTAACTATCA[A/T]CTAATCCCTTTGCCT | 5522 |
rs9993862 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367625 | TGTCAGAAATGAAAC[A/G]CCTCCTCTCATTACT | 5522 |
rs9995060 | snp | A/C | 0.0966517 | 0.197444 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354830 | GCCCACAGCCCCCCA[A/C]AGCCAGGCCCCATTG | 5522 |
rs9995412 | snp | C/T | 0.201727 | 0.245295 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6400432 | aaatctttttaactg[C/T]ctgagttttaatttc | 5522 |
rs9996640 | snp | C/T | 0.249038 | 0.249998 | downstream-variant-500B | PPP2R2C | GRCh38.p7 | 4:6320457 | TAGAGGGAGCAAACC[C/T]TTGACGTGAACCCAG | 5522 |
rs9997690 | snp | C/G/T | 0.170408 | 0.236992 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6426304 | TCCAGCTCCCTTCTA[C/G/T]GATCAGCTGCTGAAA | 5522 |
rs9998544 | snp | C/T | 0.304937 | 0.243889 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6516924 | TCTTGGCGAGTGGCA[C/T]GTAGGCAGGGCACTG | 5522 |
rs9999781 | snp | A/G | 0.4661 | 0.125701 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423308 | tcccggattcaagca[A/G]ttctcctgcctcagc | 5522 |
rs10000024 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423539 | AACCAAGAAACACAC[A/G]TGCACCCTGCCCTTA | 5522 |
rs10001231 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332552 | TCCCAGCGAGGCCTG[C/T]GCCACCCAGGACGCT | 5522 |
rs10001583 | snp | A/C/G/T | 0.117537 | 0.212022 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6523803 | ataatggccaaacaa[A/C/G/T]ggaaacaccctaagt | 5522 |
rs10002158 | snp | C/G | 0.499502 | 0.0157669 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520911 | GGCTGGGAAGTGGCC[C/G]AATGGAGACTGATTT | 5522 |
rs10003308 | snp | A/C | 0.303938 | 0.244112 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6478995 | GCAGGGAGGGCACTG[A/C]GGGTCACATGGCCAC | 5522 |
rs10003601 | snp | C/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362894 | TGCACCCCCTTTCCC[C/G]TTTGACTTTGGGTAG | 5522 |
rs10004283 | snp | C/T | 0.438526 | 0.164189 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428530 | TTGCACAGAGTCACC[C/T]GTGACTTAAGCATTA | 5522 |
rs10006700 | snp | A/G | 0.111576 | 0.20818 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422168 | ACCCAAGACTTGGGA[A/G]GTTGATGAGGCTCCA | 5522 |
rs10006805 | snp | A/G | 0.412082 | 0.190341 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6355073 | CTTTTTGCAAGCATT[A/G]ATCACTGCTTATTAC | 5522 |
rs10006854 | snp | A/G | 0.433382 | 0.169915 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422363 | CCAGCAAGCCCTGTG[A/G]CTCCGGCAAACGAGT | 5522 |
rs10007480 | snp | A/G | 0.106278 | 0.204558 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322006 | GAAGTGGAGTCCTGG[A/G]GAGGGCCACACTCCT | 5522 |
rs10007735 | snp | A/G | 0.499265 | 0.0191552 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410252 | GAGCAGGCTGGGCGC[A/G]CTTGTTCACACAGAG | 5522 |
rs10008136 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410674 | ATACACCTGCCTAAT[A/G]TCACAGGGGAGACGT | 5522 |
rs10009382 | snp | G/T | 0.266273 | 0.24947 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530893 | TCCACCAGGCTGCTG[G/T]GCACCTGTCACAGTG | 5522 |
rs10010551 | snp | C/G | 0.136166 | 0.22258 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447959 | TCTGGGATTCACTCA[C/G]TTATTCCTGATGGAA | 5522 |
rs10010682 | snp | C/T | 0.250732 | 0.249999 | downstream-variant-500B | PPP2R2C | GRCh38.p7 | 4:6320492 | CCAGTGCAAAGCCCA[C/T]GGGCATCCCCACCCA | 5522 |
rs10010715 | snp | C/T | 0.472147 | 0.114677 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430538 | TCAGAGGAGAGTGCA[C/T]GCCTCCTCGGTGCAC | 5522 |
rs10010817 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430706 | aaggcgggtggatca[C/T]atgaggtcaggagtt | 5522 |
rs10011754 | snp | C/T | 0.223225 | 0.248562 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6536378 | AGATGAAAAGCTCTG[C/T]AGAAAAGTGAGAAAA | 5522 |
rs10011998 | snp | A/C | 0.38934 | 0.207568 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6391859 | AAAGACCTGCGTTTG[A/C]ATCCCACCCTGACCA | 5522 |
rs10012796 | snp | C/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436364 | CTTTGTTTGCTCTGT[C/T]TGAGCTTTACAGCCA | 5522 |
rs10013142 | snp | C/T | 0.194902 | 0.243853 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6395841 | ATCCTGGTAGCCCCC[C/T]AGCTGCAGGCCTTGT | 5522 |
rs10013856 | snp | A/G | 0.492087 | 0.0623997 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6479142 | CTCCCAAGTTACTCA[A/G]CTCCTAAGTGGCAAT | 5522 |
rs10014119 | snp | C/G | 0.379746 | 0.213696 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6449341 | CTGCAGAGAACAGGC[C/G]CGTCTCTAAGTGCCC | 5522 |
rs10014123 | snp | A/G | 0.176219 | 0.238865 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6449353 | GGCGCGTCTCTAAGT[A/G]CCCATTCCGAGAGAA | 5522 |
rs10014493 | snp | A/G | 0.209693 | 0.246729 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354638 | AGAAACTCTGTTCAC[A/G]GTCATTTGCCCCCCA | 5522 |
rs10014501 | snp | C/G/T | 0.0688439 | 0.173476 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354678 | CAACACACACTAACA[C/G/T]GGTGCAGAAGGCAGC | 5522 |
rs10014591 | snp | A/C | 0.405603 | 0.195673 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6528221 | CTTCCCGGCCTGCAA[A/C]GCCCGCCCTGGCTCT | 5522 |
rs10015220 | snp | C/T | 0.403509 | 0.197319 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412485 | GCAGGCATGTAGATG[C/T]CAGCTGTGTGCTTGA | 5522 |
rs10015352 | snp | A/G | 0.35894 | 0.225016 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6409750 | CACCCCAAGTCATGG[A/G]TGGAGCTGGGGATAG | 5522 |
rs10015919 | snp | A/C | 0.171132 | 0.237449 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6363535 | AGTGAGCCGAGATTG[A/C]GCCACTGCACTTCAG | 5522 |
rs10017523 | snp | A/G | 0.288127 | 0.247076 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6529015 | CACGGACGCGCACTA[A/G]ACTTACTTTATTTCT | 5522 |
rs10017606 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6325552 | TTTCACACAATGCTG[G/T]TTCTTCTGATCCATT | 5522 |
rs10017768 | snp | C/G | 0.393434 | 0.20476 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6379944 | CCTCTCTTCACCCCC[C/G]GCTTCCTCCCCTCCC | 5522 |
rs10017776 | snp | C/G | 0.460702 | 0.134554 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412914 | TGTGAACCAGGCATA[C/G]GGCCTTCAACAGACA | 5522 |
rs10017964 | snp | C/G | 0.487495 | 0.0780784 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410233 | GAGTCTGCTGGAGTA[C/G]TGGGAGCAGGCTGGG | 5522 |
rs10018163 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413280 | acacattgtcatgta[C/T]ttacacatatgcatg | 5522 |
rs10018178 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430869 | ggcggaggttgcagt[A/G]agccaagatcgcacc | 5522 |
rs10018350 | snp | A/G | 0.26078 | 0.249767 | downstream-variant-500B | PPP2R2C | GRCh38.p7 | 4:6320374 | cctacaagataggtc[A/G]tcttattagctccat | 5522 |
rs10018437 | snp | A/G | 0.249038 | 0.249998 | downstream-variant-500B | PPP2R2C | GRCh38.p7 | 4:6320463 | gagcaaacccttgac[A/G]tgaacccagCTTCCC | 5522 |
rs10018521 | snp | A/G | 0.249038 | 0.249998 | downstream-variant-500B | PPP2R2C | GRCh38.p7 | 4:6320566 | CACTAAAAACAAACA[A/G]CATTCTGGACCTCGT | 5522 |
rs10021738 | snp | C/G | 0.146314 | 0.227484 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404005 | CCAACCTGCCACCAC[C/G]TAGCTGTGTGACCTT | 5522 |
rs10023932 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6563522 | gcgcgaggcggctcc[A/G]gagcggcggggccgg | 5522 |
rs10024848 | snp | A/G | 0.427423 | 0.176128 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6528354 | AGGGCCTGTGCTCAG[A/G]CCCAGGCAAGGTGGG | 5522 |
rs10025517 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362968 | ggggatattaataac[A/G]cctaccacatagtgt | 5522 |
rs10026033 | snp | A/G | 0.104859 | 0.203554 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428504 | GGGACAGGAGACAGG[A/G]AAGAAACCAATTGCA | 5522 |
rs10026710 | snp | C/G | 0.0448719 | 0.142907 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421310 | GCTGGCCTGGCCTGC[C/G]AAAGACAAGCTTGTG | 5522 |
rs10027223 | snp | A/G | 0.116838 | 0.211584 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437192 | ACTTTGCTCACTGAT[A/G]TGACCTTCCTGGTTT | 5522 |
rs10027973 | snp | G/T | 0.497329 | 0.0364438 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464360 | CCCAGGGTGCTGAGG[G/T]ATGTACAGACTCCTC | 5522 |
rs10029948 | snp | C/T | 0.423726 | 0.179776 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6452608 | CCCTAGGCTTTCAGC[C/T]GCTGCCCCAAATTAT | 5522 |
rs10030047 | snp | C/T | 0.103438 | 0.202533 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6517638 | ACAGAAGAAATTACC[C/T]TGCGGCTCTTTGGGA | 5522 |
rs10030485 | snp | G/T | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6542879 | ACAACCTTAGATATT[G/T]ACAACCCATTTGAAC | 5522 |
rs10030974 | snp | C/G | 0.0919752 | 0.193722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6477805 | GCACTGGAGTCATCC[C/G]GACTCCCACGCCTTC | 5522 |
rs10031167 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6560550 | tcaccaggttgtggc[A/G]gaaggaaagcagctc | 5522 |
rs10031697 | snp | C/T | 0.179105 | 0.239737 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6473222 | ACCTCTCCTGACGAG[C/T]GAGAAAGTTAAAGAA | 5522 |
rs10032087 | snp | C/G | 0.407674 | 0.194008 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6523429 | CAAAATGGGCAGTGG[C/G]CTTGGACACATACAT | 5522 |
rs10033049 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423526 | GGGATATTTTGGAAA[C/G]CAAGAAACACACATG | 5522 |
rs10035042 | snp | C/T | 0.0333695 | 0.124785 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6348713 | AGAAAGAAGGAGCTT[C/T]TATCTGCTGCCAGGA | 5522 |
rs10212731 | snp | A/G | 0.414741 | 0.188044 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413350 | CACACTCTCATACTC[A/G]TGCATGTGTGCACAC | 5522 |
rs10212978 | snp | A/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6559408 | cagcacacacacaca[A/C]acacacacacacaca | 5522 |
rs10213100 | snp | A/G | 0.348794 | 0.229651 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6348331 | ACATAGCACTGACCT[A/G]TGGAGCCCCTCTCCT | 5522 |
rs10213247 | snp | C/T | 0.412416 | 0.190055 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413602 | TATCAGAGCAAGACC[C/T]GACCCTGCTGTGAGA | 5522 |
rs10213410 | snp | C/T | 0.416382 | 0.186593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360087 | AACCCCAGAGAGCCA[C/T]GCCTAGCACAGACCA | 5522 |
rs10213596 | snp | C/T | 0.416545 | 0.186448 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413481 | ATCACTTATGGAGCA[C/T]ACTTAGTGAGCCCAA | 5522 |
rs10213597 | snp | G/T | 0.416382 | 0.186593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413613 | GACCCGACCCTGCTG[G/T]GAGAGAACACCCTGC | 5522 |
rs10213600 | snp | G/T | 0.416545 | 0.186448 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413654 | CCTGCACCACAGCAC[G/T]CACCTGTTCCATTCA | 5522 |
rs10213664 | snp | C/T | 0.414353 | 0.188383 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413858 | TGGCCAGCTCCACGA[C/T]GGGGACCCTCCCAAC | 5522 |
rs10446500 | snp | A/G | 0.34101 | 0.232846 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6360839 | GAAGTCCAATAACAC[A/G]GTGTTAGCAGGGCTG | 5522 |
rs10461054 | snp | A/G | 0.414245 | 0.188477 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6502990 | GCACATTCCAGAAGC[A/G]TCTTCACTGGCTCCC | 5522 |
rs10516180 | snp | C/G | 0.279726 | 0.248226 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429692 | AGCCAATTTTATGAC[C/G]GTCTCAGAGTGTTTC | 5522 |
rs10543061 | in-del | -/TG | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373902 | GTGTATGTGCATGCA[-/TG]TGTGTGTGTGTGTGT | 5522 |
rs10581214 | in-del | -/ATGT | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414076 | AAGTTTTGCCTGTGT[-/ATGT]GTGTGTGTGTGTGTG | 5522 |
rs10601452 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456307 | ATGAAGGATGTTATT[C/T]CCCCCCCCCCCCTTT | 5522 |
rs10604483 | in-del | -/AA | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6341357 | AAAAAAAAAAAAAAA[-/AA]CCCAGCTCACCCACA | 5522 |
rs10606346 | in-del | -/AA | 0 | 0 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321676 | ACAAAACCAAAAAAA[-/AA]GTTTGGATTTGGCTG | 5522 |
rs10623195 | in-del | -/AA | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387808 | CGACAACAGTGAAGA[-/AA]AAAAAAAAAAAGAGT | 5522 |
rs10641215 | in-del | -/ACCT | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455050 | AGCACAAGTCACCTA[-/ACCT]GTGCTGGAGCTGAAA | 5522 |
rs10660004 | in-del | -/GTCTG | 0.136166 | 0.22258 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374033 | AGTTGGTGTTAGTGT[-/GTCTG]TGACTCCTCCAAGGC | 5522 |
rs10691194 | in-del | -/AAAAA | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6542703 | CAAGACTCTGTCTCA[-/AAAAA]AAAAAAAAAAAGAAA | 5522 |
rs10694649 | in-del | -/AA/AAA | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387819 | AAGAAAAAAAAAAAA[-/AA/AAA]GAGTGAAGGGCAAAA | 5522 |
rs10755149 | snp | A/C | 0.496649 | 0.0407971 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6507936 | CTGAAAATCCTTAGA[A/C]GACAAATCAAATTTA | 5522 |
rs10755150 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508082 | CCTAGGCTACATAGT[A/G]AGACCCCAGTCTCTA | 5522 |
rs10755151 | snp | G/T | 0.497151 | 0.037632 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508228 | AGGCGGTTATTAAAC[G/T]GTCTCTCTAAAATAA | 5522 |
rs10804977 | snp | A/G | 0.323197 | 0.239044 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6366293 | GCCCAGGCCCGCCAG[A/G]GCCCAAAGCCCGGGC | 5522 |
rs10804978 | snp | A/G | 0.413416 | 0.189196 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6366399 | TAAGACCACATGGAA[A/G]TGGTGAACTTCCAGC | 5522 |
rs10804979 | snp | G/T | 0.459914 | 0.13578 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6396786 | TGGGGCTGGGAGGGG[G/T]TAGAGAGAAGGCCCT | 5522 |
rs10804980 | snp | C/T | 0.479984 | 0.0980171 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411125 | ATCTACCCACCTCAG[C/T]CTCCCAAAGGGCTTG | 5522 |
rs10804981 | snp | G/T | 0.356811 | 0.226034 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411135 | CTCAGCCTCCCAAAG[G/T]GCTTGGATTACAGGT | 5522 |
rs10937722 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6333476 | GGCATATGAAAGCCA[C/T]GCCTGGCTAGGAAGG | 5522 |
rs10937723 | snp | A/G | 0.142609 | 0.225759 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356243 | CCCAGCCAAGCACCT[A/G]GTACCTGTCGCAGCT | 5522 |
rs10937725 | snp | G/T | 0.491368 | 0.0651254 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411041 | ACACCTGGCTAATTT[G/T]TGTATTTTTTGTAGA | 5522 |
rs10937726 | snp | C/T | 0.435837 | 0.167226 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411044 | CCTGGCTAATTTGTG[C/T]ATTTTTTGTAGAGAT | 5522 |
rs10937728 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6441671 | CGAGGCCTCTGCTCC[C/T]CTCATGACTGCCCCA | 5522 |
rs10937729 | snp | G/T | 0.425586 | 0.17796 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6450913 | CACACCTCCATCGGC[G/T]GACACTTCAGCCCCA | 5522 |
rs10937730 | snp | C/T | 0.347473 | 0.230215 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456690 | AGCTCTGGGTGCCCC[C/T]CACGGTGAACCACGG | 5522 |
rs10937731 | snp | C/T | 0.33875 | 0.233717 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456941 | AGCCAGGTGCGGTGG[C/T]TTGCGCCTATAATTC | 5522 |
rs10937732 | snp | C/T | 0.472522 | 0.113946 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468334 | AGCAATTCCCAAGCA[C/T]CCTTCACTTCCTCAA | 5522 |
rs10937733 | snp | C/T | 0.34303 | 0.232046 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468921 | GTCCAGGGCCCAGGG[C/T]CCAGTGCCCTATCAG | 5522 |
rs10937734 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6469444 | GCACCTGGTTCTTCC[A/G]CAAACTGAATTTTAG | 5522 |
rs10937735 | snp | A/G | 0.49995 | 0.00499176 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6469519 | AATAATAACAATGCC[A/G]TGTGTTCAATGCCTC | 5522 |
rs10937736 | snp | A/G | 0.439363 | 0.163222 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6484106 | TTCACCTCCtcttct[A/G]gaagttttatagatt | 5522 |
rs10937738 | snp | A/C | 0.494013 | 0.0543839 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493795 | CACGCCCAGCCCCCA[A/C]CCTGATTAATGGTTT | 5522 |
rs10937739 | snp | C/T | 0.497881 | 0.0324789 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6507685 | ccagatcacaaactc[C/T]tgagcaaatcaatgg | 5522 |
rs10937740 | snp | A/G | 0.309894 | 0.242719 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531084 | ACCCCTCCTGGGGCC[A/G]GGAGCTGTGCCTGGT | 5522 |
rs10937741 | snp | A/G | 0.387263 | 0.208947 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6536929 | GATATCAGGTCAGGT[A/G]AGGTGGCTCACACCT | 5522 |
rs10937742 | snp | C/T | 0.489837 | 0.0705577 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6550443 | AACTTCACCCTTCAC[C/T]AACAAGCCATGCACT | 5522 |
rs11271562 | in-del | -/TGTCGTCGCCAAGTCTGCCA | 0.4444 | 0.15719 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322099 | GTTCTCCTGGACCCT[-/TGTCGTCGCCAAGTCTGCCA]TGTCCTACTTCACAA | 5522 |
rs11286848 | in-del | -/A | 0.449979 | 0.150028 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403865 | GAAACTCCGCCTCAG[-/A]AAAAAAAAAAAAAAA | 5522 |
rs11303171 | in-del | -/C | 0.187685 | 0.242109 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444382 | TTCTTATTCAGTCTT[-/C]CTGACAACCCCAAAG | 5522 |
rs11306059 | in-del | -/C | 0.347473 | 0.230215 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6530544 | GTCGCTGGACTGTCA[-/C]CCACCACGCAACTGA | 5522 |
rs11317671 | in-del | -/A | 0.498082 | 0.0309114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406599 | ACTAAAGAAAAAGCC[-/A]AAAAAAAAATAGCTG | 5522 |
rs11322332 | in-del | -/A | 0.0479149 | 0.147179 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434793 | GCCTATACGATAGAT[-/A]AAAAAACAGTATCTT | 5522 |
rs11323274 | in-del | -/A | 0.253824 | 0.249971 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406591 | CTGTCTCTACTAAAG[-/A]AAAAGCCAAAAAAAA | 5522 |
rs11327901 | in-del | -/T | 0.375 | 0.216506 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531562 | TCTTTCCCGTTTTCC[-/T]TTTTTTTTTTTTTGG | 5522 |
rs11330202 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430954 | AACAACAAAAAAAAA[-/A]CTTTGCAGATCCCTG | 5522 |
rs11358702 | in-del | -/A | 0 | 0 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321669 | AAACAAAACAAAACC[-/A]AAAAAAAAGTTTGGA | 5522 |
rs11421592 | in-del | -/C | 0.0387552 | 0.1337 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455915 | CTCCCAGGCTGCAAC[-/C]GGGCCCACTGCATCC | 5522 |
rs11428044 | in-del | -/A | 0.0733688 | 0.176922 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6321491 | TCATTCACGTTGATT[-/A]AAAAAAAAATCAATG | 5522 |
rs11430012 | in-del | -/C | 0.124144 | 0.21601 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6478525 | GTACAAATAACAGGG[-/C]CCCTGTTCGATGTGC | 5522 |
rs11430416 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6465661 | TCAAATTTAAAAAAA[-/A]AAAAAGCTTAAACTC | 5522 |
rs11433028 | in-del | -/A | 0.4973 | 0.0366419 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6503795 | TTAAAAAAAAAAAAA[-/A]CAAAAACTGAGAATT | 5522 |
rs11461620 | in-del | -/G | 0.496279 | 0.0429702 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404657 | GAGGGATGCTGGTGT[-/G]GGGCCCAGGAAGCTG | 5522 |
rs11545013 | snp | A/C | | | synonymous-codon | PPP2R2C | GRCh38.p7 | 4:6323353 | CATTGCCATTGCCGC[A/C]ACCAACAACCTGTAC | 5522 |
rs11554991 | snp | A/C | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322316 | GGAACCCTTAGGATC[A/C]CCTCTGTCCACGAGA | 5522 |
rs11554992 | snp | A/G | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322536 | GGTGCTCAGCCCTAG[A/G]GGCAGTTGACTTACC | 5522 |
rs11721516 | snp | A/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374009 | TTTGCTTCTAGGTTG[A/T]GTGCCTGGGAGTTGG | 5522 |
rs11721574 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415219 | CTGGCCAGCGCCAGC[A/G]TGTCCACTGTTACAG | 5522 |
rs11721690 | snp | A/G | 0.497907 | 0.0322805 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6505764 | tgaggtcaggagttc[A/G]agaccagcctggcca | 5522 |
rs11722046 | snp | G/T | 0.413416 | 0.189196 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412802 | GAGGTCATGAGGGTG[G/T]AGCCCCCATGAATGG | 5522 |
rs11722260 | snp | A/G | 0.408188 | 0.193589 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402552 | ACGCCCTCCATTTCC[A/G]TAGACATGTCCTATG | 5522 |
rs11722264 | snp | A/G | 0.412249 | 0.190198 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402573 | ATGTCCTATGGGACC[A/G]CGCTAGGCCAGGAGT | 5522 |
rs11722385 | snp | G/T | 0.444931 | 0.15653 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414978 | CCATAGGAACCCAGG[G/T]TCCACAGAAGAGCAT | 5522 |
rs11722804 | snp | C/T | 0.136166 | 0.22258 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520157 | GTGGATGAAGGGGTA[C/T]GCTGGGGAGTTGAGA | 5522 |
rs11722835 | snp | C/T | 0.341685 | 0.232581 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520247 | AGGAGGAGGGAGGCA[C/T]GGAGTGGACACTCAG | 5522 |
rs11723119 | snp | C/T | 0.363776 | 0.222609 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6419992 | AAATAAGGTCACATT[C/T]TGAGGTTCCAAGTGG | 5522 |
rs11724327 | snp | A/G | 0.416382 | 0.186593 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414679 | AAGGGAGAAGGGAGG[A/G]GAACTCTTGTTGGGC | 5522 |
rs11724328 | snp | A/G | 0.414245 | 0.188477 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414710 | TCCTAATGTATCCAC[A/G]AGGCCCTGGGCTGGA | 5522 |
rs11724341 | snp | A/G | 0.499722 | 0.0117779 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468939 | AGTGCCCTATCAGCT[A/G]CACTGCTCTCCCCAC | 5522 |
rs11724359 | snp | A/G | 0.414245 | 0.188477 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414791 | CACTCCTTCCTGGCT[A/G]TGCAACCTCAGGCCA | 5522 |
rs11724710 | snp | G/T | 0.406641 | 0.194842 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368978 | ATATAGATGCAGACG[G/T]GGAGACAGGATTCAA | 5522 |
rs11724762 | snp | C/T | 0.396727 | 0.202413 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432178 | GTCCCTCCCCATCCT[C/T]ATGGCTATGGTCTTT | 5522 |
rs11725306 | snp | C/G | 0.215446 | 0.2476 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6392715 | CGGGAGAGGCCTGAG[C/G]ATTTTATTCTGCATG | 5522 |
rs11725341 | snp | A/G | 0.39325 | 0.204889 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415134 | GCATGCGCCTCGTCC[A/G]CATGCTGGAGGACCT | 5522 |
rs11726287 | snp | A/G | 0.485392 | 0.0842056 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421471 | CTAAGTGTTTGATAA[A/G]TGTTTGTGGATTACC | 5522 |
rs11726572 | snp | A/G | 0.0930568 | 0.194599 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416377 | CCAGGTCTGACTCAA[A/G]GCCTCTTTCCACCAT | 5522 |
rs11726600 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6554979 | aaagagaaagaaaga[A/G]aagagaagagaagag | 5522 |
rs11727636 | snp | C/T | 0.499961 | 0.0043928 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6555544 | CCCACCTGCTGTGTG[C/T]TGTCTGGAGGCCGGT | 5522 |
rs11727760 | snp | A/G | 0.49306 | 0.0584955 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6350333 | TTACTGAACTTCACT[A/G]AAGTGGGATCCAGAG | 5522 |
rs11727834 | snp | A/G | 0.477768 | 0.103061 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6350547 | TTGCGTCATCAGGAC[A/G]CTCATTCTCGTTGTA | 5522 |
rs11729808 | snp | A/G | 0.283684 | 0.24772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6327380 | GGAGAGCCCAGGCCT[A/G]GACACCACTGTCAGC | 5522 |
rs11730007 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6492640 | AGTAGACTGGAGCCC[C/T]CATCCCTACAGCAGG | 5522 |
rs11730177 | snp | A/G | 0.497211 | 0.037236 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354786 | CCTGAGCCCGGGTGC[A/G]TGATTGCGAATCCAG | 5522 |
rs11730405 | snp | C/T | 0.341909 | 0.232492 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6392673 | CTCAGAGAGGTGGGC[C/T]GGGCCGGGGTCCTGC | 5522 |
rs11731070 | snp | C/T | 0.272511 | 0.248984 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367441 | TCCCCTGGCTCTGCG[C/T]GGACACAGGCCTCCT | 5522 |
rs11731075 | snp | A/G | 0.428786 | 0.174744 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534366 | CACATCAATACGTAC[A/G]CTAacacacaccaac | 5522 |
rs11731119 | snp | C/G | 0.496034 | 0.0443518 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6355123 | CTATCTGTCCCCAGC[C/G]AGGGCAGGGACCTGC | 5522 |
rs11731255 | snp | A/G | 0.497271 | 0.0368399 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493971 | TTTTTTAATCCAAAC[A/G]TGCTCATTTGCCCCA | 5522 |
rs11731327 | snp | A/G | 0.499354 | 0.0179596 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6559204 | TCAGATCCATCTCTC[A/G]CTGCTAAGCAGCCTG | 5522 |
rs11731355 | snp | A/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6503069 | gcaactctccttaaa[A/C]taatgtccaaatctt | 5522 |
rs11731380 | snp | A/C | 0.41441 | 0.188333 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412905 | GTCGCCACCTGTGAA[A/C]CAGGCATACGGCCTT | 5522 |
rs11731465 | snp | C/G | 0.41441 | 0.188333 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413174 | ATGAAATCACACGCT[C/G]TCACACTCACATTCA | 5522 |
rs11732607 | snp | A/C | 0.235564 | 0.249583 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6539304 | gagaagaggctggga[A/C]agattccccccataa | 5522 |
rs11732749 | snp | C/G | 0.49334 | 0.057322 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6527167 | AATATTTCCATTCCT[C/G]CCTAGAATTCCAAAC | 5522 |
rs11732798 | snp | C/T | 0.499722 | 0.0117779 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468914 | CTCCAGGGTCCAGGG[C/T]CCAGGGCCCAGTGCC | 5522 |
rs11733043 | snp | A/G | 0.243061 | 0.249904 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6541314 | aCTGTCCTATCCTCC[A/G]TTCTCCAAAATAGCT | 5522 |
rs11733217 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390148 | GTACTTCCAGGGGAC[A/G]GGGGAGAGCTGCTTA | 5522 |
rs11733237 | snp | A/C | 0.0923359 | 0.194016 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6541758 | tggtctcaaactcct[A/C]gcctcaagtgatcca | 5522 |
rs11733363 | snp | C/G | 0.209084 | 0.246629 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6392809 | GGACGAGCACTTTCA[C/G]GGGTGGGCGTGGACC | 5522 |
rs11733876 | snp | A/G | 0.41275 | 0.189769 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436644 | TGCTCCATATGAGTC[A/G]TTGACATGAACCAAG | 5522 |
rs11733883 | snp | C/G | 0.497907 | 0.0322805 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6505690 | CAAGAATAAggccag[C/G]tgtggtggctcacgc | 5522 |
rs11733886 | snp | A/C | 0.498084 | 0.0308911 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6505710 | gtggctcacgcctgt[A/C]atcccaccactttgg | 5522 |
rs11734044 | snp | A/G | 0.343254 | 0.231956 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6336102 | GTTTATCCACTAATA[A/G]GTGGTGTCATATTTT | 5522 |
rs11734695 | snp | A/C | 0.48155 | 0.0942576 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421333 | AGCTTGTGCTTCCTA[A/C]TTCTGGGATTCCCAG | 5522 |
rs11735266 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494693 | CACAGGGAGGCATCA[A/G]CTGGGAGCAGGGCAG | 5522 |
rs11735902 | snp | C/T | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437439 | GTTTCATTTTAAAGA[C/T]GGGGGAACTACAGCC | 5522 |
rs11736148 | snp | C/T | 0.417845 | 0.185278 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447222 | GGAGCCAGCCACTCT[C/T]GGGTCGGTGCCTCCC | 5522 |
rs11736449 | snp | C/T | 0.497959 | 0.0318836 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6513750 | CCCATGAAAAGGGCG[C/T]GCACTGGGCCACACC | 5522 |
rs11736549 | snp | C/T | 0.415235 | 0.18761 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413003 | TCTGTTGTTTATGAA[C/T]CACCCAGTCTATGGT | 5522 |
rs11736839 | snp | A/G | 0.48679 | 0.0801892 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6335670 | GAAGTTCCAGCACCC[A/G]GTGGGCCAGGGCTGC | 5522 |
rs11737367 | snp | C/T | 0.449345 | 0.150869 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508567 | gcactccagccctgg[C/T]gacggagtgagactc | 5522 |
rs11737674 | snp | C/T | 0.440057 | 0.162414 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408336 | CCTCCCCTTCCCTGG[C/T]GCCTAACTACCCCCG | 5522 |
rs11737849 | snp | A/G | 0.332337 | 0.236052 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6545590 | CCTGGTTCCCATCCC[A/G]GCTCAGACATGAATG | 5522 |
rs11930441 | snp | A/G | 0.337841 | 0.23406 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6500682 | GGGTTCATTTGAGCC[A/G]AGTCCTGGGGTGCAT | 5522 |
rs11930718 | snp | A/G | 0.171704 | 0.237423 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402701 | GATGGAGGGAGACAT[A/G]GGGATTCTGAGGGCC | 5522 |
rs11932296 | snp | A/T | 0.44333 | 0.158505 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422584 | CAAGGTGTCAGCAGG[A/T]TGGTTTCTTCTGAAG | 5522 |
rs11932964 | snp | C/T | 0.20111 | 0.245173 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356039 | GTGGTCTGGGAAGCA[C/T]GTCACACGTGCTGCG | 5522 |
rs11933328 | snp | A/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6482732 | ttaacccacttgctg[A/T]ctagtcgttagttcc | 5522 |
rs11933395 | snp | C/T | 0.104859 | 0.203554 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6517820 | GGGTTCCAATACCAG[C/T]TCCCCTACCTACAAA | 5522 |
rs11935416 | snp | C/T | 0.275464 | 0.2487 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6393671 | ACAAGGGACAGGGAT[C/T]GGGGAGGCCAGGGGC | 5522 |
rs11935460 | snp | A/C | 0.0444908 | 0.142359 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428677 | ATAAGCCAGACATCA[A/C]TGACACTGCAAATGC | 5522 |
rs11936718 | snp | G/T | 0.338296 | 0.233889 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6382238 | GCTAGTAGGAGCCCG[G/T]GATGGCCCGCTGCTG | 5522 |
rs11938118 | snp | A/G | 0.308414 | 0.24308 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6478742 | TAGAAGACCACAGCC[A/G]TGAATGACCCTCCAA | 5522 |
rs11938125 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6478783 | CTTCAAGGCTATTTC[G/T]CACTCCTGCTGCGTG | 5522 |
rs11938694 | snp | C/T | 0.455024 | 0.143057 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356283 | GGCCGGCTGGCTGGG[C/T]GGGACTAGCTTCGCA | 5522 |
rs11939028 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6424590 | TCGCCAGGCAGTGTC[A/G]ATACATTGACACAGG | 5522 |
rs11939569 | snp | C/G | 0.442385 | 0.15965 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6349081 | GATCAGAATCTCTTG[C/G]AGCATGCAAGGACTG | 5522 |
rs11940264 | snp | A/C | 0.207559 | 0.246371 | upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6564115 | CCCACCCACCGGTCC[A/C]GCGGCAGCCGCCTCC | 5522 |
rs11940918 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430904 | cactccagcctgggc[A/G]acagagcaagactct | 5522 |
rs11941149 | snp | A/G | 0.264358 | 0.249587 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6526543 | AATGGTTAAATTGGT[A/G]AAAAGAAAAGAAGAG | 5522 |
rs11941241 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6394589 | CAAAATGGCAATAAG[A/G]GTCACCCCTGCCGCA | 5522 |
rs11941709 | snp | A/G | 0.127254 | 0.217792 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356047 | GGAAGCACGTCACAC[A/G]TGCTGCGGGTCCAGT | 5522 |
rs11942129 | snp | C/T | 0.496746 | 0.040204 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334241 | GCTGAGCCCTACTTA[C/T]AGGTGGGTTTTGTTT | 5522 |
rs11942139 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429357 | ATAATCAATAATCAA[C/T]TAACAGTGACTTTCA | 5522 |
rs11942931 | snp | C/G | 0.389715 | 0.207315 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332720 | GGATGATGGCTCCTT[C/G]TCACCGGACAGTAAA | 5522 |
rs11943607 | snp | G/T | 0.097727 | 0.198275 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433150 | ttaagtttttgggga[G/T]tcaaaagttgtatgt | 5522 |
rs11945944 | snp | C/T | 0.437118 | 0.165792 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416831 | AAGCCTGCTGGGCTC[C/T]CTGTGTGTGCCCCAG | 5522 |
rs11946327 | snp | C/T | 0.472147 | 0.114677 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407107 | gggaacgtaggccta[C/T]ggacaccatgatttt | 5522 |
rs11946417 | snp | A/G/T | 0.0592355 | 0.161582 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6489860 | GCATCCACTATTTTC[A/G/T]AACTTAATACCAAAG | 5522 |
rs11947214 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6518756 | ggtgaaaccccatct[C/T]tactaaaaatacaaa | 5522 |
rs12163752 | snp | A/G | 0.25801 | 0.249872 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447807 | TCTCCGTTTTCTCCC[A/G]TGCCTCAGCTACGGC | 5522 |
rs12498383 | snp | C/T | 0.336245 | 0.234652 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6424113 | CCTCACAGGGAAAGC[C/T]GGATTAGGAGGAAGG | 5522 |
rs12498555 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6344875 | TATTCTAGTACATGG[A/T]TGTCATCACTGTCGA | 5522 |
rs12499788 | snp | A/C | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6324974 | AGGAAATCCTGTTTC[A/C]TTTTGGAAGCTGAGC | 5522 |
rs12500662 | snp | A/G | 0.137527 | 0.223271 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6352741 | ATTTTTCTCCACTGC[A/G]GTGGGTTGAATAATG | 5522 |
rs12500979 | snp | C/T | 0.42666 | 0.176893 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6452285 | CAGATCCTGTGAACA[C/T]TGGCAGTGGAGTCTA | 5522 |
rs12501097 | snp | C/G | 0.169435 | 0.236663 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404653 | TTGCAGAGGGATGCT[C/G]GTGTGGGCCCAGGAA | 5522 |
rs12501177 | snp | A/T | 0.380529 | 0.213219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416863 | GGAAGGCTCCTGGCC[A/T]CTCTCCCTTCCCCCT | 5522 |
rs12501278 | snp | C/T | 0.444931 | 0.15653 | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322091 | GCGTCTCAGTTCTCC[C/T]GGACCCTTGTCGTCG | 5522 |
rs12502427 | snp | A/G | 0 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6545988 | GGGTTGCGTGGGGCA[A/G]TTTCCAGAGAAGCAT | 5522 |
rs12503917 | snp | A/C | 0.453818 | 0.144769 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531400 | AGGTGCAGGAAGACC[A/C]CCAAGTGTGCCCAAA | 5522 |
rs12504065 | snp | A/G | 0.222333 | 0.248464 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6352488 | GTCCCCTTTCCCCTG[A/G]CAAAGCTGCTTGAAT | 5522 |
rs12505438 | snp | A/G | 0.158632 | 0.232706 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6554267 | acacagagacagaca[A/G]gcacagggagaaagg | 5522 |
rs12505462 | snp | C/G | 0.192715 | 0.243348 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6536744 | GTAAATCTCACTCTT[C/G]TGTCAAGAACAATCA | 5522 |
rs12505766 | snp | C/T | 0.433673 | 0.1696 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6401776 | AAGTCACAAGTGACA[C/T]TGGAGAACAGCGCTA | 5522 |
rs12507333 | snp | C/T | 0.345925 | 0.230864 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433652 | CCCTGGGTTCAACTA[C/T]ACATGCAGTCACTAT | 5522 |
rs12508505 | snp | G/T | 0.16028 | 0.233346 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6562475 | AACGGAGTCGGGGGG[G/T]GGGGTTGGATATTTG | 5522 |
rs12509025 | snp | G/T | 0.48679 | 0.0801892 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6331832 | TCCAGACTCCCTGTT[G/T]TGGGAGAAAAATAGC | 5522 |
rs12509174 | snp | A/G | 0.336017 | 0.234736 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6457466 | agcctcaacctcctg[A/G]gttcaagtgatcctc | 5522 |
rs12510309 | snp | C/T | 0.431769 | 0.17164 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6400201 | TTGAGGATAGATGTT[C/T]GACAATACCTCAACC | 5522 |
rs12510934 | snp | A/G | 0.480618 | 0.0965156 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434199 | ACCCTGAGCTGTCAC[A/G]TTCTTTTCATTGCTA | 5522 |
rs12511002 | snp | C/T | 0.0085257 | 0.0647315 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6375956 | CAGAACAAAATAAAG[C/T]GAGTCACATAATTAA | 5522 |
rs12511611 | snp | C/T | 0.373196 | 0.217538 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6452333 | GGATTTTCCTCACTT[C/T]CCAGCTCCTGGGGCC | 5522 |
rs12511721 | snp | C/T | 0.435915 | 0.167139 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372741 | GAGGTGAAGGCCAGG[C/T]GGTGGCATCAGGACA | 5522 |
rs12511794 | snp | C/T | 0.380529 | 0.213219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416864 | GAAGGCTCCTGGCCT[C/T]TCTCCCTTCCCCCTG | 5522 |
rs12511900 | snp | C/G | 0.145642 | 0.227177 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6352233 | GTCTTGGCTGTCACT[C/G]GGGGCCCCCGGCTGG | 5522 |
rs12512657 | snp | A/G | 0.416055 | 0.186885 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6539748 | GCAGGCGGAAGCTGC[A/G]CTAGGCATTCCCGAT | 5522 |
rs12640531 | snp | C/T | 0.343477 | 0.231866 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6445773 | CTTCACTAATGCAAG[C/T]GACCCAAGAGGTGCT | 5522 |
rs12641138 | snp | A/G | 0.427271 | 0.176281 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468663 | TGGCTGAGCTCCTGT[A/G]TCTTGGTCATCACTG | 5522 |
rs12642135 | snp | C/T | 0.15665 | 0.231917 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6352071 | ATGCCCAAACTCAGC[C/T]ACCGTGAACACAGCT | 5522 |
rs12642310 | snp | G/T | 0.453453 | 0.145282 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6406996 | gaggaggaggtgatg[G/T]aaaaaccgaagcaga | 5522 |
rs12642889 | snp | C/G | 0.435122 | 0.175825 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6533638 | TGCAGTTGACATTGC[C/G]GTCCAAATGCAGGAT | 5522 |
rs12643897 | snp | C/T | 0.451234 | 0.14834 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494600 | CCCCTAACTCAGACA[C/T]TCACAGCCCAGGTGG | 5522 |
rs12644059 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6459043 | GAATCCATGACTCTT[C/T]CAGTTACCCACTGCt | 5522 |
rs12644113 | snp | A/G | 0.499683 | 0.0125759 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6476842 | atttttcattgttgt[A/G]taatattctatggca | 5522 |
rs12645711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436740 | TCACAACTACTCAAC[C/T]CTGCTGTTGTAGTGT | 5522 |
rs12647372 | snp | C/T | 0.426966 | 0.176587 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468638 | CTGGTCAGCCTGAAC[C/T]ACCTCCCCTTGGCTG | 5522 |
rs12647442 | snp | C/G | 0.486133 | 0.082104 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6391422 | GAATCCTCTGCACAC[C/G]CGCTGGGCCTCGCCA | 5522 |
rs12647559 | snp | C/G | 0.49607 | 0.0441545 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361686 | GTCACCCCCTGGGAG[C/G]ACTAGGAGGGTCTGT | 5522 |
rs12651082 | snp | A/T | 0.416218 | 0.186739 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414437 | GGGGCGAGGGAAGTC[A/T]CGCAGAAAGCAGGAG | 5522 |
rs12651287 | snp | A/G | 0.355311 | 0.226737 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374339 | CCAAACCAGAGCTCA[A/G]AACCAGTTTTTTAGT | 5522 |
rs13103536 | snp | C/G | 0.480064 | 0.0978296 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6424424 | TGCAGAGAGAGGACA[C/G]TTTGTGGTCCTCCAT | 5522 |
rs13104457 | snp | C/T | 0.201418 | 0.245234 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368994 | GGAGACAGGATTCAA[C/T]CCTTCTGATGAATGA | 5522 |
rs13105372 | snp | A/T | 0.3752 | 0.216391 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6528339 | TGAACAGGGGCTTCC[A/T]GGGCCTGTGCTCAGG | 5522 |
rs13105375 | snp | C/G | 0.491368 | 0.0651254 | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6348966 | TGAGCAACTCGTCCG[C/G]GGTGGCCCAGGTGTG | 5522 |
rs13105491 | snp | C/T | 0.252983 | 0.249982 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6479433 | ACCCACAACCCAGGT[C/T]GCCATGCCTCTGGAC | 5522 |
rs13106868 | snp | G/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6342368 | ccacatcattccagg[G/T]tcaagtgTATTCAAC | 5522 |
rs13108451 | snp | A/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6342370 | acatcattccagggt[A/C]aagtgTATtcaactt | 5522 |
rs13109641 | snp | C/T | 0.453087 | 0.145793 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415758 | GAAGGTCATCCAGTC[C/T]AACCCTCTCTGGTGT | 5522 |
rs13109678 | snp | C/T | 0.359575 | 0.224707 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6484947 | ttgcactagctataa[C/T]gtcgagaagaatgtg | 5522 |
rs13109953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6337797 | GCGCTGGCCCTTGTC[A/G]CCCCACTGCTGGCTG | 5522 |
rs13111231 | snp | C/T | 0.153665 | 0.230694 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6485716 | aatatatactaatgt[C/T]accttctcattcttg | 5522 |
rs13112194 | snp | A/G | 0.119281 | 0.213102 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6325583 | TAGTGGAAGGAGAGC[A/G]ACATAATTAAAGTCA | 5522 |
rs13112391 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413514 | CAACCCATCTCAGCC[A/G]GTAATTAAACCTGCC | 5522 |
rs13113183 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403099 | CTAATTAGAACCACT[A/G]AGCAGTCTGAAGACT | 5522 |
rs13113366 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6428330 | GTTAGAGCAACTCCA[C/T]AAGACCTGCTCACCG | 5522 |
rs13114034 | snp | A/G | 0.131038 | 0.219882 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6522707 | GCACCAGTTTCTGAT[A/G]CCACAGGATGCTGAG | 5522 |
rs13114468 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402994 | GCTCTGCATGTCTCC[C/T]GGCTCACTCACACCT | 5522 |
rs13115077 | snp | G/T | 0.401747 | 0.198678 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461725 | CTGGTATTAATCAGA[G/T]TAACAAACTGTCTTC | 5522 |
rs13115486 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410640 | TGTGAGGGGGTGTGG[C/T]TGGACGTGAAGCAAC | 5522 |
rs13115734 | snp | C/G | 0.34101 | 0.232846 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368162 | GGCTCAGATTCTTTG[C/G]TCAATAATCATTATT | 5522 |
rs13116164 | snp | A/G | 0.444267 | 0.157354 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422598 | GATGGTTTCTTCTGA[A/G]GCCTCTCTCCTGGCT | 5522 |
rs13116228 | snp | C/T | | | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556588 | agggcacaaatacct[C/T]atgctctgcagtcat | 5522 |
rs13117055 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6485999 | attgattaggaactt[C/T]cttctattccaatat | 5522 |
rs13117823 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6398524 | catcatcagtcatca[A/C]aagacgcagatgcaa | 5522 |
rs13120438 | snp | C/T | 0.100231 | 0.200173 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334202 | CAGTAGTTATCTCTG[C/T]TCATGGTGTCCTGGG | 5522 |
rs13120740 | snp | C/T | 0.373196 | 0.217538 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6452258 | GGTGACACCGCAGGT[C/T]CCCATCAGCTCCAGA | 5522 |
rs13121398 | snp | C/T | 0.405776 | 0.195535 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6539738 | GAGTGTCCCTGCAGG[C/T]GGAAGCTGCACTAGG | 5522 |
rs13122678 | snp | G/T | 0.117188 | 0.211804 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6535021 | CAAGGAGGTGGCGCA[G/T]GAAGGGGGCCTCACC | 5522 |
rs13122929 | snp | A/G | 0.324855 | 0.23853 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361881 | GCTCCATGATCGATC[A/G]ATGGCCTAAGAGAGA | 5522 |
rs13124487 | snp | A/G | 0.499693 | 0.0123764 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362584 | TGTCTCAACAAAGCT[A/G]GGCAGGCCATCAGAA | 5522 |
rs13124495 | snp | A/G | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6323025 | AGAACCCTGAACTGT[A/G]AGACTCCACAGTCAT | 5522 |
rs13127385 | snp | C/T | 0.384401 | 0.210799 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532900 | AGGGAGGCTGGGAGA[C/T]GCATCCCCAGCATTG | 5522 |
rs13128187 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432897 | ctgcaagaccaaccc[A/G]tcctcttccttctcc | 5522 |
rs13129045 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6415699 | TGCAGAAGCGGGCAG[C/T]AGTGAGGGGCTTTGA | 5522 |
rs13129773 | snp | A/G | 0.119978 | 0.213528 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463711 | TCCTGCCCAGAATGC[A/G]CTAGAATACCATGTC | 5522 |
rs13130362 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6424352 | CCAGGTGAAAACAGA[A/G]TGGTCTTTAAATCTT | 5522 |
rs13130860 | snp | C/G | 0.343254 | 0.231956 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6528466 | TGAATCATCAGAGAG[C/G]GTTCCTCCACTCGAC | 5522 |
rs13135169 | snp | A/G | 0.450105 | 0.149859 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534734 | TGCACCCTGTACTTC[A/G]CAGTGACAACCCCGC | 5522 |
rs13135461 | snp | C/T | 0.452227 | 0.146984 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416255 | TTAGGTGCACACAAC[C/T]GCCCCCACGATGTGT | 5522 |
rs13135605 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534278 | CCACATAGCAAGaca[C/T]acacatatcccaaca | 5522 |
rs13136126 | snp | G/T | 0.153665 | 0.230694 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6484647 | cactcatttaggtct[G/T]ctttaatttctatca | 5522 |
rs13136605 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6424921 | CCCAGCTGTGTGGCC[A/G]CAGAACAGCAGGCAG | 5522 |
rs13138424 | snp | C/T | 0.474813 | 0.109357 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354614 | CCCTGGGAACAGCCC[C/T]TCCAATTTAGAAACT | 5522 |
rs13140794 | snp | A/G | 0.308908 | 0.242961 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6535123 | GGGTCGGGGGCCCAG[A/G]GGCCAGAGCAGGGGA | 5522 |
rs13141184 | snp | A/G | 0.44547 | 0.155857 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6535252 | CGCTGCTGCCCGGCT[A/G]TGAGAACGGGCTTCT | 5522 |
rs13142248 | snp | C/T | 0.312837 | 0.241974 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6535112 | GGCAGGAGCCAGGGT[C/T]GGGGGCCCAGGGGCC | 5522 |
rs13143101 | snp | A/G | 0.402277 | 0.198272 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461698 | CCCTGGAATGTGGGG[A/G]TTTCTTTGTAACTGG | 5522 |
rs13143875 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6529851 | CTCTGCTTGGGAAGG[C/T]CTCCCATGACAAGGA | 5522 |
rs13144738 | snp | C/T | 0.383632 | 0.211288 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407543 | gggacaacaggcacc[C/T]gccaccacacccggc | 5522 |
rs13145709 | snp | A/C/G | 0.00755907 | 0.0610114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6544811 | AAGAAGCAAATTAGC[A/C/G]CAAACTCCCAGAAGC | 5522 |
rs13146368 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6402935 | CCCTCTGCAAAGCCA[C/T]GAAGGCCTGCCAAGA | 5522 |
rs13147522 | snp | G/T | | | utr-variant-3-prime | PPP2R2C | GRCh38.p7 | 4:6322898 | AAGCAGCTCCCATCA[G/T]CTCCGGTCCCTGCAA | 5522 |
rs13148109 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6410932 | GAAGTGCGGTGGTGC[A/G]ATCTCTGCTCACTGC | 5522 |
rs13148161 | snp | A/T | | | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6556530 | tgcgcacacgtgcag[A/T]gatcctattggccct | 5522 |
rs13149248 | snp | C/G | 0.122411 | 0.214991 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6470970 | GCCCGCGCCCGCGCT[C/G]GCGCTGCGCTCCCCG | 5522 |
rs13149260 | snp | G/T | 0.341909 | 0.232492 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368183 | AATCATTATTTTCAC[G/T]CTCTTGCACACACCA | 5522 |
rs13149326 | snp | C/T | 0.392881 | 0.205147 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6536014 | TCACAGTGTTAGTCC[C/T]GCACCACCCCCACCC | 5522 |
rs13149858 | snp | C/T | 0.494896 | 0.0502606 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456306 | AATGAAGGATGTTAT[C/T]TCCCCCCCCCCCCTT | 5522 |
rs13150377 | snp | A/C | 0.486067 | 0.0822953 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6441415 | AGCCCGCCCCATGAG[A/C]CCCATGGGGCCTCCA | 5522 |
rs13150637 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6401348 | GTATTGTCAGGAACC[A/G]TCTTTGGACTGCCTC | 5522 |
rs13152451 | snp | A/G | 0.463774 | 0.129618 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423897 | TCAAATGTTTTGAGA[A/G]TGTGTTAGGGTTAGG | 5522 |
rs13434456 | snp | A/G | 0.394171 | 0.204242 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6412671 | TTTGCAGCCCTGCAG[A/G]GAGAAGGCTGATTGA | 5522 |
rs16835101 | snp | C/G | 0.482234 | 0.0925596 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6441318 | ACCACAGTGACCCTT[C/G]TAAACCCAACTCTGG | 5522 |
rs16838576 | snp | C/T | 0.0587695 | 0.161031 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6334012 | AGAAGGTGGTAGAGT[C/T]GGGATTTGAAGCCAA | 5522 |
rs16838603 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362797 | ATCATGACTGAGAGG[C/T]GGTGTAGCATGACAG | 5522 |
rs16838608 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6364896 | TGGGATCACAGGACT[C/T]ATCGAGGCTTGAGCA | 5522 |
rs16838612 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6365442 | CTTGTCTACACGGCA[C/T]CAGGCCCCATACTCA | 5522 |
rs16838645 | snp | C/T | 0.106278 | 0.204558 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6368628 | TTACAGCCAACCTGT[C/T]TGAATGTCTTGTGGC | 5522 |
rs16838648 | snp | A/G | 0.147656 | 0.228091 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6370837 | GCCCGATGTCCTTTC[A/G]GCTTCAGTGGAGGGT | 5522 |
rs16838651 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372826 | TCCATCCTGATCCTC[C/T]GTGGTCTGAAATAGG | 5522 |
rs16838654 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373395 | ACGAACTTTCATCTC[A/G]GACAGTTGGTGCGAG | 5522 |
rs16838658 | snp | A/G | 0.415727 | 0.187175 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373542 | ATCAGCTACGGGAGC[A/G]AGGCGTCACCTCTTG | 5522 |
rs16838673 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6374999 | GAGAAAAATCTCCAA[C/T]GCTGGGAGGGACATA | 5522 |
rs16838684 | snp | C/T | 0.00507753 | 0.0501297 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6378623 | TGACCTGCAGGGCGA[C/T]GGCTAGGACCTCCGG | 5522 |
rs16838698 | snp | A/C | 0.495135 | 0.0490805 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6384312 | GTAATGATCTACATC[A/C]GTGATTATAGCCATG | 5522 |
rs16838703 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6385309 | CTAGTGGATGTTTAA[C/T]GTCTACTCATTTTTA | 5522 |
rs16838704 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6385373 | AGTTGCCTCTCTTGA[A/G]TGCCAGAAATTCTCA | 5522 |
rs16838707 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6385905 | TGTGTGCTCTTCACT[A/G]GGTACTGACACTTCC | 5522 |
rs16838718 | snp | A/G | 0.153997 | 0.230832 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6395509 | GAGGCTCCGTGTCTC[A/G]GTCTCTGGAGGACAG | 5522 |
rs16838719 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6397162 | ACCCCTGTAAGAGAA[A/G]CGTGGCCCTTCCAAA | 5522 |
rs16838721 | snp | A/C | 0.169435 | 0.236663 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399824 | TGGGCAGCCGACAGA[A/C]AGTCAAATGCAGAAC | 5522 |
rs16838722 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6400662 | GTAACTAAGGCGTCT[A/G]TTGATGTAAGCAACA | 5522 |
rs16838740 | snp | A/G | 0.455977 | 0.141681 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407821 | AGGATACAAAGTAAA[A/G]CCATCATTTAGTGCT | 5522 |
rs16838760 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411519 | CCTCTTAAGTTCTCT[A/G]ATTTGTGTCTGTACT | 5522 |
rs16838780 | snp | C/T | 0.453209 | 0.145623 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6416058 | TGCTGTCACCCTGGG[C/T]CTTTCTATTTGGATT | 5522 |
rs16838785 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6420795 | AGACCTCGACGATGA[C/T]GGCACAGATAAGTAT | 5522 |
rs16838796 | snp | C/T | 0.0433465 | 0.140692 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421970 | AGGAAAGAAATCCCA[C/T]AATGTTTCAAGAAGA | 5522 |
rs16838803 | snp | A/C | 0.0648419 | 0.167978 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423603 | AAACAGGTAAACAGA[A/C]CCAAAAAATAATCAT | 5522 |
rs16838806 | snp | G/T | 0.0607341 | 0.163335 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425444 | CTCCTCATGAGTCAT[G/T]TGAGGATCCAGGGAC | 5522 |
rs16838833 | snp | A/G | 0.119281 | 0.213102 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6429801 | AAACAAATGCCCATC[A/G]TTGCCAGAAAGAACG | 5522 |
rs16838840 | snp | A/C | 0.110872 | 0.20771 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437416 | TTTTGTAGTTGTCTG[A/C]TTCAACTGTTTCATT | 5522 |
rs16838844 | snp | G/T | 0.493247 | 0.0577133 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6438893 | AGTGGTATCCAGGTG[G/T]TCCCTGACACAGTGC | 5522 |
rs16838845 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6439795 | TGGACATGACACTCT[C/G]AGGAGTCCTTACCAA | 5522 |
rs16838849 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6446784 | GCAGGCATGGCAGGC[A/G]CTGCTGTTACCATTC | 5522 |
rs16838853 | snp | A/G | 0.388587 | 0.208071 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6449223 | TTCGCAGCACCGTGC[A/G]AAACGGGAAAAAAAC | 5522 |
rs16838880 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6460587 | TTACAAAATAGGATA[C/T]GCACACAGTAGATGC | 5522 |
rs16838885 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461628 | AGACTCCTGGGCCAA[C/T]TGGGATCATCCACAA | 5522 |
rs16838891 | snp | A/G | 0.254105 | 0.249966 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6462676 | TCATAAAATGGACCA[A/G]AATTTAGGTAACAAA | 5522 |
rs16838965 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6549748 | AGCCCACGGATGAGC[C/T]TTAAGGTATGAGCTA | 5522 |
rs17721365 | snp | G/T | 0.084364 | 0.187256 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6383339 | ATCGCAGATGCAAGA[G/T]GATGAAAACATTTAC | 5522 |
rs17721635 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6391567 | GTATTGATTTGTGTT[A/G]AAGGCCATGGAAAAA | 5522 |
rs17721784 | snp | C/G | 0.43221 | 0.171171 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6399732 | TCGGATGCTGAGAAA[C/G]GCAGAGTGAGGACCG | 5522 |
rs17722523 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6425942 | TGTGTGTTGCGGGGA[A/G]AGGCACTCTATGGCT | 5522 |
rs17722973 | snp | A/G | 0.479904 | 0.0982045 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6439688 | ACCATGAACAGAGAG[A/G]TCTTCCTAAACTAAA | 5522 |
rs17723995 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6463874 | TCGATTGCCTTTCAT[C/T]GCAACACAGATAGCA | 5522 |
rs17778826 | snp | A/G | 0.363359 | 0.222822 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423581 | TACCACTGGGGAGGC[A/G]AAGCCCAAACAGGTA | 5522 |
rs17779293 | snp | C/T | 0.32768 | 0.237625 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6438777 | GAGCAGAAACACCTG[C/T]GCTTGTCTTTGGTTA | 5522 |
rs17779465 | snp | A/G | 0.133093 | 0.220981 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6444643 | CAGGTCCTAAGCGGG[A/G]GCCCAGTTTCTTAAT | 5522 |
rs17779675 | snp | C/T | 0.366885 | 0.220993 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447787 | AGCCTCTGAACTTCT[C/T]GGGGTCTCCGTTTTC | 5522 |
rs28392508 | snp | A/G | 0.3752 | 0.216391 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534032 | CCCCAACACACACAT[A/G]TCAACAAGCACACAC | 5522 |
rs28392771 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6494583 | GAGTGACACAAACCC[A/C]GCCCCTAACTCAGAC | 5522 |
rs28396928 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332863 | AGATCTTACCCATCC[C/T]TCAAGGCCCAGCACA | 5522 |
rs28403035 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361409 | AAAACCCAGAGCTTG[A/T]AAGTCCAGCCCCACT | 5522 |
rs28414604 | snp | A/C | 0.142947 | 0.22592 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6345649 | GAAGAGGCAGGGAAA[A/C]CGGTGCTCCCCAGAG | 5522 |
rs28417776 | snp | A/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387799 | CCAGCCTGGGCGACA[A/T]CAGTGAAGAAAAAAA | 5522 |
rs28418897 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6436219 | CTTACAAGCCACCCA[A/G]TCTATGGTATTCTGC | 5522 |
rs28419045 | snp | A/G | 0.381113 | 0.21286 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407488 | GCAACCTCGCCTGCT[A/G]GGTTCAAGCGATTCT | 5522 |
rs28427021 | snp | C/T | 0.242201 | 0.249878 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6545416 | CCATGAGGGACCAGG[C/T]ATGCCAGAAGACTAA | 5522 |
rs28430849 | snp | A/G | 0.039522 | 0.134904 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6407498 | CTGCTGGGTTCAAGC[A/G]ATTCTCCAGCTTCAG | 5522 |
rs28442878 | snp | A/G | 0.130008 | 0.219321 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6509420 | GGGGGAAAAAAAGTC[A/G]AAATGTTATTCAGAA | 5522 |
rs28445758 | snp | A/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6503809 | TTAAAAAAAAAAAAA[A/C]AAAAACTGAGAATTC | 5522 |
rs28452787 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332569 | CCACCCAGGACGCTT[C/T]CCTACTAGGTCTTCG | 5522 |
rs28459760 | snp | C/T | 0.117886 | 0.21224 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6532579 | CCCTTAAATGCACAT[C/T]CCACTCTGCGTTTTT | 5522 |
rs28479689 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6330846 | AGGCTACCTGACTCC[C/T]GCCTGGGGCCCTGCT | 5522 |
rs28489627 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512475 | GGTGATTATGGTGGT[A/G]GTGGTGGTGATGGTG | 5522 |
rs28491260 | snp | A/G | 0.411578 | 0.190768 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6339263 | AGCTCCCTTGGGCCA[A/G]GGGTCCTGCCTTGGT | 5522 |
rs28498274 | snp | C/G | 0.0197687 | 0.0974348 | upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6565464 | GGAGACAGGCATGCA[C/G]GTAATAATACATTCA | 5522 |
rs28499281 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6352079 | ACTCAGCTACCGTGA[A/G]CACAGCTTTCTGCCC | 5522 |
rs28510277 | snp | C/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6451573 | TGGGTTATAAATCCA[C/T]CCAGCCTGTGTTATG | 5522 |
rs28519448 | snp | G/T | 0.0729998 | 0.176553 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6527084 | TGAATCTCAGCTCCA[G/T]TGTAAATCGCTTGAT | 5522 |
rs28521834 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6518855 | TTGAACCCGAGAGGT[A/G]GAGGTTGCAGTGAGA | 5522 |
rs28526512 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6332857 | ACGGCCAGATCTTAC[C/T]CATCCTTCAAGGCCC | 5522 |
rs28527220 | snp | C/T | 0.431325 | 0.172108 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414605 | TGTCAAAGAGCCCTA[C/T]GAGATGGGCAGGGGG | 5522 |
rs28538353 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434340 | GTCATTTCTCACCTG[C/T]GTATTTCTTTTTTCT | 5522 |
rs28548874 | snp | C/T | 0.488545 | 0.074807 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6533586 | CGTTAATGCCTATGA[C/T]GCACAGCTGCTTAAG | 5522 |
rs28550773 | snp | C/T | 0.485255 | 0.0845871 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408868 | GCCTCTCAAGGATCC[C/T]GTGGCTTTTTTTTTT | 5522 |
rs28552815 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6361091 | GGAGTTAGGGTTTCA[A/C]CATATGAATGGGGAT | 5522 |
rs28554153 | snp | A/G | 0.166506 | 0.235645 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403181 | TTACTGCCGCTGGCC[A/G]GGCTGTCGCTCTCAT | 5522 |
rs28555191 | snp | C/T | 0.322483 | 0.239262 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6547193 | TTGCCTATTTTTTCT[C/T]CACTGGAGATTTTAA | 5522 |
rs28555652 | snp | C/T | 0.232359 | 0.249377 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6545338 | ATAAGTTAATTTACC[C/T]CCACTAACAAGGTGC | 5522 |
rs28559735 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6446794 | CAGGCGCTGCTGTTA[C/T]CATTCAGCAGATGAC | 5522 |
rs28571819 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6379469 | GCTTAGAAGTTCTCC[A/G]ATATTTTTGCCTCTA | 5522 |
rs28574983 | snp | C/G | 0.465473 | 0.126772 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6534362 | GCCACACATCAATAC[C/G]TACACTAACACACAC | 5522 |
rs28575591 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6339141 | CTGTGCATATTGTTC[A/G]CATGCTCTCTAAAGA | 5522 |
rs28589582 | snp | A/G | 0.439918 | 0.162576 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422451 | TAGAGAGAGCTTGAA[A/G]AATTAAATTTGGTAA | 5522 |
rs28599721 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6392684 | GGGCTGGGCCGGGGT[C/G]CTGCACCCAGCAGGC | 5522 |
rs28607039 | snp | A/G | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6557505 | CTCTGGAGAGAGGAC[A/G]TGGAAGCTGCGACCT | 5522 |
rs28609566 | snp | C/G | 0.212728 | 0.247206 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531873 | GCCGGTGGCCCAGGT[C/G]CGGAGCAGGTGGCAG | 5522 |
rs28610561 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458780 | GACACGTTGTGGGAT[C/G]GGACCCTGGGCTATG | 5522 |
rs28615984 | snp | C/T | 0.234982 | 0.249549 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6545682 | CTGAGCAACCCTCTT[C/T]TTCTAAGAATCCCCA | 5522 |
rs28622408 | snp | C/T | 0.470618 | 0.117591 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6356484 | TCCAGAGTGCAATCC[C/T]TGCCCCCTGACCATC | 5522 |
rs28637289 | snp | A/G | 0.263535 | 0.249633 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6527225 | ACCAACTCGCTGAGC[A/G]ACCTTGGCCAGGGAG | 5522 |
rs28654333 | snp | C/G | 0.030665 | 0.119967 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6418882 | TCATGCCTGGTTCTG[C/G]GGAGTAAAGTGTGAA | 5522 |
rs28668758 | snp | A/G | 0.0197687 | 0.0974348 | upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6565465 | GAGACAGGCATGCAG[A/G]TAATAATACATTCAT | 5522 |
rs28689807 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6506207 | AACTGATTGAAAGAG[A/G]AGCAAGGGATTTTTT | 5522 |
rs28735473 | snp | C/T | 0.436976 | 0.165952 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6455044 | ATAATGAACACAGCA[C/T]AAGTCACCTAGTGCT | 5522 |
rs28736564 | snp | C/T | 0.134802 | 0.221877 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6510693 | TTAGAAAATGTTTGT[C/T]GAGGCCGGGCACGGT | 5522 |
rs28767570 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6504788 | AGTTAAAATAATAAC[C/T]CAGCCTCAGGAACCT | 5522 |
rs28778583 | snp | C/T | 0.49706 | 0.0382258 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6504537 | TATTTGTACTATGCT[C/T]AAGAATGTAAAGGAA | 5522 |
rs28785197 | snp | A/G | 0.384401 | 0.210799 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387231 | TGGTAAAAGACATCA[A/G]TTTACAAATTTAAGA | 5522 |
rs33935112 | in-del | -/T | 0.110167 | 0.207236 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434926 | CATTCTTCTATTGAA[-/T]TTTTTTGGGGGTTCT | 5522 |
rs33943020 | in-del | -/TT | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531575 | CCTTTTTTTTTTTTT[-/TT]GGCTAACACTTATGG | 5522 |
rs33943664 | in-del | -/A | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6350671 | TCCAGGTTCTCTCCC[-/A]AGGGGAGACCTCTCC | 5522 |
rs33951633 | in-del | -/C | 0.167809 | 0.236103 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430944 | AAACAACAACAACAA[-/C]AAAAAAAAAACTTTG | 5522 |
rs33964031 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362895 | CACCCCCTTTCCCCT[-/G]TTGACTTTGGGTAGA | 5522 |
rs33996768 | in-del | -/T/TT | 0.656622 | 0.0532959 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6422053 | GGCACATTGGTGCAA[-/T/TT]TTTTTTTTTTTTTTA | 5522 |
rs33999687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423704 | GATAAGCTGAGGAGG[A/G]TCTCAGGGTGAGGAG | 5522 |
rs34004229 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6437632 | TTGACTAGAATGTAC[-/T]TTTTAAAGACTCACG | 5522 |
rs34006454 | snp | A/G | 0.191775 | 0.243125 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6405724 | TGCTGACATGACAAC[A/G]TCACGAAAACCTCAT | 5522 |
rs34007201 | multinucleotide-polymorphism | CA/TG | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6353488 | ACAGCCCCCCCACAC[CA/TG]ACAACCCCCCACACC | 5522 |
rs34056063 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6487466 | TTGAAAGATTATTTT[-/T]CTGGGTATGAACTCT | 5522 |
rs34075489 | snp | C/G | 0.154993 | 0.231244 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6508379 | ATCACGAGGTCAGGA[C/G]TTTGAGACCAGACTG | 5522 |
rs34077531 | snp | C/G | 0.366885 | 0.220993 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6448777 | GCTGTCCTCCTCCCC[C/G]CAGTGAGCAAAGGAA | 5522 |
rs34083488 | snp | A/G | 0.225005 | 0.248747 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461937 | AGGCCCACGGAGCAC[A/G]TGGCATGCACCATCT | 5522 |
rs34084084 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6522781 | GTTCTTGGCTAATAT[-/A]CTGCTGAGCCAGACA | 5522 |
rs34119137 | snp | A/C | 0.26271 | 0.249677 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6354044 | CTTCCTCATTCTAAG[A/C]CCTTCCCTTGTCCAG | 5522 |
rs34129740 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6501927 | GCCCAGCACATAGCA[A/G]GTGCTTAGAAAGCAT | 5522 |
rs34133176 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520177 | GGAGTTGAGAGGGGT[-/G]CCTAAGAACCTCAAG | 5522 |
rs34145628 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6457227 | GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 5522 |
rs34155275 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6336420 | GTCTCAATCCCCGAG[-/C]CCCTCGTGTGGCCTT | 5522 |
rs34156385 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6417846 | AGCCATCAGGAAAGC[C/T]TCAGAGAAGTCGCCG | 5522 |
rs34156583 | snp | C/T | 0.400504 | 0.199621 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6458292 | ATATCATAGACCGGG[C/T]GGCTTATAAACAACA | 5522 |
rs34164549 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6493837 | GACTCTTTAGTCGGG[-/G]AGCCGTAGCTTTAAA | 5522 |
rs34165459 | snp | A/G/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512512 | GTGGTGGTGGTGATG[A/G/T]TGGTGGTGGTGGTGG | 5522 |
rs34167130 | in-del | -/AC/C | 0.5 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6430943 | AAAACAACAACAACA[-/AC/C]AAAAAAAAAAACTTT | 5522 |
rs34183926 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404980 | GCAAAATAAGAACCA[-/T]TGGACGTGACCTCCT | 5522 |
rs34195451 | snp | C/T | 0.434109 | 0.169127 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6380662 | ATGCAGGCAGCTCTC[C/T]GCAAACATCGGCTGA | 5522 |
rs34209889 | in-del | -/T | | | intron-variant, utr-variant-5-prime | PPP2R2C | GRCh38.p7 | 4:6413970 | GCTCCCTGGTGGCTC[-/T]TGCAGTTGGCTACTG | 5522 |
rs34210845 | in-del | -/T | 0.454784 | 0.1434 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6411555 | CTGACTTTTCATTTC[-/T]TTTTTTTTTTTTTTT | 5522 |
rs34213120 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6423977 | CGTCCATTCACTGCC[C/T]ACCTGGCTGTCCTGG | 5522 |
rs34213661 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6452242 | CCATCTGTCCCTTCA[-/G]GGTGACACCGCAGGT | 5522 |
rs34225532 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6378275 | ATTTACATGCTGCTC[-/A]AAAAGGATATTATTT | 5522 |
rs34231840 | snp | A/G | 0.106633 | 0.204807 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372766 | AGGACATAGCATGCC[A/G]TGAGCATGTGATCCC | 5522 |
rs34239735 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6370421 | CTGGAGCTCCTGCTA[-/G]GGAGACCGCCCCTCC | 5522 |
rs34249624 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6442962 | CAGCTAAGGAGACTG[-/A]AAGCTTGGAGATCTT | 5522 |
rs34286120 | snp | A/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512500 | ATGGTGATGGTGGTG[A/G]TGGTGCTGATGTTGG | 5522 |
rs34292067 | in-del | -/TTT | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6434360 | TCTTTTTTCTTTTCT[-/TTT]TTTTTTTTTTTTTTT | 5522 |
rs34299480 | snp | A/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6355550 | AAAGCCACAGAAAGC[A/C]CAAAAAAAAAAAAAA | 5522 |
rs34330982 | snp | C/T | 0.089084 | 0.191327 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6467108 | GAAATGGAGCCCACA[C/T]TCGCTGTGAAGCCCA | 5522 |
rs34332993 | in-del | -/C | 0.084728 | 0.187577 | intron-variant, upstream-variant-2KB | PPP2R2C | GRCh38.p7 | 4:6421726 | ACTGGCACTCGGAGG[-/C]CCAGCCTCCCTGGGG | 5522 |
rs34341188 | snp | C/T | 0.385359 | 0.210185 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6540380 | TGTGTTCAAGGTTCA[C/T]TGATGTTGTAGCGTG | 5522 |
rs34346847 | snp | C/T | 0.120326 | 0.21374 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6325249 | GGGACATAGGCTGAA[C/T]ACCCCGCACAGTGCT | 5522 |
rs34356207 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6439442 | GAAATCTAACTTTAG[C/G]GTGATTCAAAATAGC | 5522 |
rs34373521 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6414359 | ATCATGTGCACGGTG[A/G]GCATTCTGTGGAAAC | 5522 |
rs34377646 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6365680 | TCTTCAGGCAGGCAT[-/G]GGGCTGATGAAGGTT | 5522 |
rs34392038 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6483788 | AATTTTGATGAGGCC[-/A]AATTTATTAATTTTT | 5522 |
rs34392821 | snp | G/T | 0.119978 | 0.213528 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6461985 | ATCCCAGAGAGGATG[G/T]TGCAGCCACGCTCAC | 5522 |
rs34395449 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6371402 | CCTGCCTCCCCTGCT[-/C]CCCCACAGCTATCCC | 5522 |
rs34400800 | snp | C/T | 0.443195 | 0.158668 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6432803 | TCTTGGATTTTAGAA[C/T]ACAGTTGACCCTCAA | 5522 |
rs34407208 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6344991 | TTCCTAATACTTCAA[-/G]GGAGCAGATATATTA | 5522 |
rs34409647 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6390262 | CCTGGGGGATTGAGC[-/A]AAGCCACAGGATGCT | 5522 |
rs34448087 | in-del | -/A | 0.160938 | 0.233598 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6358646 | CTTAAACAAATTTAC[-/A]AAAAAAAAATCAAAC | 5522 |
rs34454284 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6367836 | TGAATAGATCCAATC[-/G]GGGGAGGTTTCCATG | 5522 |
rs34455575 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6396997 | GCTCAAAAAATTCCT[-/A]AAAAATGTAACTATT | 5522 |
rs34487196 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6479443 | AGGTTGCCATGCCTC[-/C]TGGACGGAGAGAAAA | 5522 |
rs34507047 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6468799 | GCTAAGTACTGAGGC[-/G]CTGCCGCAAAAAGAG | 5522 |
rs34511807 | snp | A/G | 0.5 | 0 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6345310 | TGGGCGGGAGGCGTA[A/G]GTGGGGGGGCAGTGT | 5522 |
rs34522611 | snp | C/G | 0.375 | 0.216506 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6326538 | GGTAACCTGGGGAAG[C/G]GCAGGCCTGCCAATA | 5522 |
rs34529396 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6447673 | TCTGTAACAACATCC[-/T]TTCCGTCGCCCTTTT | 5522 |
rs34529519 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6393308 | GATTTTGCCTACTCT[-/G]GGATATTTTGCATAA | 5522 |
rs34537057 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6413630 | AGAGAACACCCTGCC[A/G]CCTCTCAGCCTGCAC | 5522 |
rs34538495 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6408410 | ACTGATTGGATCAAG[-/A]AGGTAGCCACACCCT | 5522 |
rs34541141 | in-del | -/A | 0.41441 | 0.188333 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6465655 | TGTCAATTCAAATTT[-/A]AAAAAAAAAAAGCTT | 5522 |
rs34546579 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6482707 | AATTTTGGCTTTTCC[-/T]TTGCTGTCCTTAACC | 5522 |
rs34549432 | in-del | -/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6520059 | TGTTATTCCCCAGGG[-/T]AGCCCCCAAGGCGCT | 5522 |
rs34554720 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6492414 | TTGATGGGGTAGGGG[-/G]ATGCTATAAGAGCCT | 5522 |
rs34558361 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6372824 | GTCCATCCTGATCCT[-/C]CCGTGGTCTGAAATA | 5522 |
rs34560015 | snp | A/G | 0.380529 | 0.213219 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6531097 | CCAGGAGCTGTGCCT[A/G]GTGGCACCAAAGGCA | 5522 |
rs34567708 | snp | A/G | 0.322721 | 0.23919 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6464660 | ACCTAATGTTGATCA[A/G]CATGTGGTTAAAGAG | 5522 |
rs34580019 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6433878 | GAACAGCTGACTCTA[-/G]GAGCTTATGGTCACA | 5522 |
rs34580020 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6404220 | AAGGTCCTTAGAGGT[-/C]CCCCCCCTCCCATAC | 5522 |
rs34580487 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6348553 | TTCTGACCACAGTAT[-/G]GGAGATTCTCCTTTG | 5522 |
rs34585147 | in-del | -/A/AAAAAA | 0.484632 | 0.086302 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6359624 | TAAAAAAAAAAAAAA[-/A/AAAAAA]GAAACTCCTTCATCT | 5522 |
rs34589910 | in-del | -/G | 0.131723 | 0.220251 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6362894 | GCACCCCCTTTCCCC[-/G]TTTGACTTTGGGTAG | 5522 |
rs34596014 | snp | C/T | 0.25634 | 0.24992 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6542228 | GCACTAAACAAGGCA[C/T]GCCGCAGACAGAGGC | 5522 |
rs34606814 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6333166 | TTACGGATGCACCCT[-/G]GGGAGGGCAACGCTT | 5522 |
rs34610960 | snp | G/T | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6456938 | ATGAGCCAGGTGCGG[G/T]GGCTTGCGCCTATAA | 5522 |
rs34618602 | snp | G/T | 0.497907 | 0.0322805 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6466094 | TGCCTTGGAGCATTA[G/T]TTGAAAGCATGGCCC | 5522 |
rs34650552 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6341509 | GCAAATGTCTTAATC[C/T]CTCTGTGCTTCAATG | 5522 |
rs34683289 | snp | C/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6512506 | ATGGTGGTGGTGGTG[C/G]TGATGTTGGTGGTGG | 5522 |
rs34701749 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6365905 | AGGTCCATCCGCTGA[-/G]GACCTCCTGTGCAAT | 5522 |
rs34709133 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6387679 | TTATCCGGGCATGGT[-/G]GCGGGCGCCTGTAAT | 5522 |
rs34734222 | snp | A/C | 0.154661 | 0.231107 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6496058 | TGTATCTCCCTAACC[A/C]CCCTCTCTTTTCTCT | 5522 |
rs34735512 | in-del | -/A | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6373807 | GCCTGTGTGTGTGGG[-/A]AGTGTGCATGGCTGA | 5522 |
rs34761114 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6453497 | CCCCACCCCACCCCA[-/G]GGGCAGACACATGGT | 5522 |
rs34785431 | in-del | -/G | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6403380 | GCTTCCTGCCCCCTA[-/G]GTGTTTTTATTTGAT | 5522 |
rs34817087 | in-del | -/C | | | intron-variant | PPP2R2C | GRCh38.p7 | 4:6330128 | GGAGAGAGGGTGACA[-/C]CCCCAGGACCTGCAT | 5522 |
rs34820531 | snp | A/G | 0.149999 | 0.229128 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6500798 | ACACCCTGAAGCTGG[A/G]GACAAATTGCTCTAA | 5522 |
rs34821140 | in-del | -/G | 0.0543475 | 0.155628 | intron-variant | PPP2R2C | GRCh38.p7 | 4:6380529 | CCCGCTCCCCAGTCT[-/G]GCCAGGACAACGCAG | 5522 |