SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs15509 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146611150 | tgtagggtttctgcc[A/G]agagatccgctgtta | 5521 |
rs48624 | snp | A/G | 0.312837 | 0.241974 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606212 | CAACAGCCTGCACCT[A/G]TGGTTACCTAATCTC | 5521 |
rs48625 | snp | A/G | 0.287867 | 0.247116 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146606307 | CCATGTAGAGGGGTT[A/G]GGAGGGGCCCAAGAC | 5521 |
rs152436 | snp | A/G | 0.249886 | 0.25 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831342 | actcggctaattttt[A/G]tatttttagtagaga | 5521 |
rs160967 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146803933 | agcactttgggaggc[C/T]gaggcaggcagatca | 5521 |
rs160968 | snp | C/T | 0.489492 | 0.0717183 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829614 | GTACCTGCAGTGGCC[C/T]ATTTCATAGAGACAC | 5521 |
rs160969 | snp | C/T | 0.233527 | 0.249457 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837254 | ctactacaaaatcat[C/T]tcatgcaaagcctat | 5521 |
rs160970 | snp | A/G | 0.234692 | 0.249531 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836216 | CAAACATTGGAAAAC[A/G]TAACCAGTGACATAC | 5521 |
rs160971 | snp | A/G | 0.233527 | 0.249457 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146836145 | TATAAGGTCTTCAGA[A/G]TAATTCTGCCTACTA | 5521 |
rs160972 | snp | A/G | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786196 | TATAATAAACGGAAG[A/G]AAAAAAAGAATCACT | 5521 |
rs160973 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788192 | GTCTAGCTATATTTT[A/G]TCTTGGAGGAGGAAG | 5521 |
rs160974 | snp | A/G | 0.483199 | 0.0901004 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146789948 | ATAACTAGGTCTGCA[A/G]GGATAATGGGTAGAG | 5521 |
rs161021 | snp | A/G | 0.17138 | 0.237316 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146829544 | GGGCTGTGATGGGGA[A/G]CACTCTGCTGTCATG | 5521 |
rs161022 | snp | A/G | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837315 | agcccatttaaagta[A/G]gctaggcttagttat | 5521 |
rs161023 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837744 | gtgtattttacactt[G/T]cagcacatctcaaat | 5521 |
rs161024 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146837750 | tttacactttcagca[C/T]atctcaaatgaaata | 5521 |
rs161025 | snp | C/T | 0.492087 | 0.0623997 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146816766 | catatgggtctCTGA[C/T]TTTAAAAACTGACAA | 5521 |
rs161026 | snp | C/T | 0.260504 | 0.249779 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773796 | TAAAATTGGCCTCTA[C/T]GGTAAAAATATTTCA | 5521 |
rs161027 | snp | A/G | 0.25634 | 0.24992 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773937 | TGGGAATGTTTACAG[A/G]TAGGAGAAACAAGGA | 5521 |
rs161028 | snp | A/G | 0.256897 | 0.249905 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774544 | taggcatgagtcacc[A/G]cacccagccttataa | 5521 |
rs161029 | snp | C/T | | | intron-variant | PPP2R2B | GRCh38.p7 | 5:146774659 | cagctaatttttgta[C/T]ttttagtagagacgg | 5521 |
rs161030 | snp | A/T | 0.498525 | 0.0271165 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146778317 | CCTCTATGAAATTGT[A/T]ATATGGAAAATAAAG | 5521 |
rs161031 | snp | A/G | 0.499325 | 0.0183582 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146779340 | ACGGATTACTCTGCT[A/G]GCGGTTGATTCTTGG | 5521 |
rs161032 | snp | C/T | 0.497803 | 0.033074 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146781408 | ACTTGAATATTCCAT[C/T]TGCCTGTCTGATGCC | 5521 |
rs161033 | snp | A/T | 0.459687 | 0.136129 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146785712 | AAAGTCAGATAAGTT[A/T]TGGAAGTAAATCCTT | 5521 |
rs161034 | snp | C/T | 0.499451 | 0.0165644 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786190 | taaaaCTATAATAAA[C/T]GGAAGGAAAAAAAGA | 5521 |
rs161035 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786375 | GGTTGCCAAGTGAAG[C/T]GCTCCTGGAGACAGT | 5521 |
rs161036 | snp | A/G | 0.365024 | 0.221967 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146786815 | TCTTTAGAGAAAGAT[A/G]AAGTTGCCTGAAAGC | 5521 |
rs161037 | snp | C/T | 0.499937 | 0.0055907 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146787512 | cctctcttttctctt[C/T]tctcctctcctctct | 5521 |
rs161038 | snp | C/T | 0.184838 | 0.241358 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146788472 | GGGCACAGTGGCTCA[C/T]GCCTCCCAGCACGTT | 5521 |
rs161039 | snp | A/G | 0.474453 | 0.110094 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146799468 | ACACCCAAAATATAC[A/G]GTTTTGTAAGGAGGT | 5521 |
rs161040 | snp | C/T | 0.187369 | 0.242028 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146804569 | CACTCAATAAATATT[C/T]GCCGGATGGATTACT | 5521 |
rs161041 | snp | C/T | 0.224116 | 0.248656 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146805388 | TGGGATCCTTGAATG[C/T]TGTTTTCAAAAGTAG | 5521 |
rs161042 | snp | C/T | 0.187369 | 0.242028 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146806311 | AGGAAATGTATTCTT[C/T]TCCCTGATAGTTTGA | 5521 |
rs167634 | snp | C/T | 0.395453 | 0.203331 | intron-variant, nc-transcript-variant | PPP2R2B, LOC105378214 | GRCh38.p7 | 5:146913011 | ACAGGGCTGAACACA[C/T]AGTGTTTTTAACAAC | 5521 |
rs167635 | snp | A/G | 0.488241 | 0.0757703 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146881333 | ATTATAAAACGCTGT[A/G]GGACATGAAAAAGAC | 5521 |
rs167723 | snp | A/C | 0.223522 | 0.248594 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146592626 | GAACAGTTCAGATTA[A/C]TGCCAAGTAGGCTTT | 5521 |
rs170333 | snp | G/T | 0.110167 | 0.207236 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850323 | TTTCAAAAATACTAT[G/T]CTGGCTGCAGTGCAA | 5521 |
rs171618 | snp | A/G | 0.256619 | 0.249912 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146839057 | AATTGGAAGTTATAA[A/G]AAGGGAAGGTTGGAA | 5521 |
rs173637 | snp | A/C | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146832379 | tgtgccatttttaat[A/C]ttttttttttttttt | 5521 |
rs173638 | snp | A/C | 0.265727 | 0.249505 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146838663 | TTCTGTCTAGTCTAT[A/C]CTCATTCCTCTTTTT | 5521 |
rs178547 | snp | C/T | 0.399253 | 0.200558 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937315 | tactagtaacccccc[C/T]ttttttttttttctg | 5521 |
rs178549 | snp | A/G | 0.478603 | 0.101197 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146916427 | GAAGAATGAAGGAAA[A/G]TCACCTGCTTTAGTT | 5521 |
rs178594 | snp | C/T | 0.241627 | 0.24986 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146775545 | aacaagacaaagatg[C/T]ctgcttttatcactt | 5521 |
rs178727 | snp | G/T | 0.237593 | 0.249692 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146603656 | CTATTACCCAAGGAA[G/T]GAAAATAATTCCTGG | 5521 |
rs178729 | snp | C/T | 0.36955 | 0.219562 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146643927 | tgcaaagttgaatag[C/T]ggtggcaaaggccca | 5521 |
rs182649 | snp | A/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146792665 | aaaaggcaacactta[A/T]agccttgaagaagta | 5521 |
rs182697 | snp | A/G | 0.45843 | 0.138046 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146667628 | ATATTACAGATCATC[A/G]AGACTGAAATGGAGC | 5521 |
rs183665 | snp | A/G | 0.492823 | 0.0594727 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146784888 | TAGGATTAGACATAC[A/G]TAAGTTAGATACCAA | 5521 |
rs186458 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146793875 | GTCTCCCTGTGTTTA[A/G]ATACCTCAGCCCTTA | 5521 |
rs186459 | snp | C/T | 0.474453 | 0.110094 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986460 | GRCh38.p7 | 5:146868397 | GAGACTGGGAAAACA[C/T]GGCCATAGGCTTTAA | 5521 |
rs186523 | snp | C/T | 0.382473 | 0.212016 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146628517 | TCTTGAGGGCCAGGG[C/T]GAGGAGCCAGGGTTC | 5521 |
rs189785 | snp | G/T | 0 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146648216 | CTGTAAAAGGGGAAG[G/T]TCATGGAAGATCACA | 5521 |
rs193897 | snp | A/G | 0.297636 | 0.24542 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773257 | GGAATGCAAACGGCT[A/G]TGCAGTATGGCCATT | 5521 |
rs193898 | snp | A/G | 0.260504 | 0.249779 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772537 | AAGAATATAGACAAA[A/G]AAGTTGTTATCCCCT | 5521 |
rs223100 | snp | C/G | 0.487933 | 0.0767327 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146850253 | CACGTGATTTACTCA[C/G]ATGAAACTGACACAA | 5521 |
rs225180 | snp | C/G | | | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146610811 | aggctttgctcattt[C/G]tttttattctttttt | 5521 |
rs225181 | snp | C/T | 0 | 0 | intron-variant | PPP2R2B, CTB-99A3.1 | GRCh38.p7 | 5:146614276 | agccagttttcccag[C/T]accatttattaaata | 5521 |
rs249898 | snp | A/G | 0.284733 | 0.247575 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146813073 | ATATGTCCTGGCTGG[A/G]TGATTCACCAGATGT | 5521 |
rs249899 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146812791 | atatatatatataca[C/T]acatatacacacaca | 5521 |
rs249900 | snp | A/T | 0.239614 | 0.249784 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833350 | AGGTTTACTAATAAT[A/T]TCATTGTCATCTTTA | 5521 |
rs249901 | snp | A/G | 0.234692 | 0.249531 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146833664 | AAGCTCTGGTGAATG[A/G]GTATTAATGAGATGG | 5521 |
rs249902 | snp | A/G | 0.233235 | 0.249437 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146834036 | TCTTACTGCTTCTCC[A/G]ATTACATTAAACTAT | 5521 |
rs249903 | snp | C/T | 0.178465 | 0.239547 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808043 | tgatctcaggtgatc[C/T]gcctgcctcagcctc | 5521 |
rs249904 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146773492 | CTCCACTTTTAGTAT[C/T]TGGTTGAAACAGAAT | 5521 |
rs249905 | snp | A/T | 0.257176 | 0.249897 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146772239 | GACATATAAATCATC[A/T]ATAAATGTTTGCTGT | 5521 |
rs249906 | snp | A/T | 0.260504 | 0.249779 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771869 | GCAAGTgaaaagagc[A/T]tggaatactttttat | 5521 |
rs249907 | snp | C/T | 0.425432 | 0.178112 | intron-variant, upstream-variant-2KB | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146771294 | TGTCAAGTCACTTAA[C/T]ATGGCCTTTGAAATT | 5521 |
rs249908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146767531 | tgtgtgtatgtatgt[A/G]tgtatTGGAGTCATA | 5521 |
rs249909 | snp | C/T | 0.295343 | 0.245854 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766907 | GCCACCTCACCTGGC[C/T]AATTTTTGTATTTTT | 5521 |
rs249910 | snp | A/G | 0.260227 | 0.249791 | intron-variant | PPP2R2B, LOC107986461 | GRCh38.p7 | 5:146766534 | ATAATAATGGCTGCT[A/G]TGTTATCAGAAGGAA | 5521 |
rs319137 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146928476 | gaattaagaataact[C/T]gattttttttttggt | 5521 |
rs319138 | snp | C/T | 0.488786 | 0.0740357 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927860 | cggctactcagggaa[C/T]aggagagagtaggca | 5521 |
rs319139 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146927699 | tcatcttctgatcca[C/T]ataatggctgcctgg | 5521 |
rs319140 | snp | C/T | 0.48666 | 0.0805725 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926487 | ggagaatggcataaa[C/T]ccgagaggcggagct | 5521 |
rs319141 | snp | G/T | 0.479258 | 0.0997024 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926179 | aagaaaaaaaagtgt[G/T]acccatactcaagaa | 5521 |
rs319142 | snp | A/G | 0.488118 | 0.0761554 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146926102 | caaaaatttcaaggc[A/G]gctattataaatatt | 5521 |
rs319143 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848984 | acaccgaaatcaact[A/G]gaagagctcctaatg | 5521 |
rs319144 | snp | C/T | 0.206947 | 0.246265 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146848598 | ggtacctttgattga[C/T]gtgataggatggaaa | 5521 |
rs319145 | snp | C/T | 0.5 | 0 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146808994 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCACCCACT | 5521 |
rs319146 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146939452 | TTCAACTTTTGCCAT[C/T]GCTTAAATGGTAAAT | 5521 |
rs319147 | snp | A/G/T | 0.639393 | 0.10073 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146937039 | gctgggattacagac[A/G/T]tgagcaaccacacct | 5521 |
rs319148 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146831667 | agtagctgggattac[A/G]ggcatgtgccaccac | 5521 |
rs319149 | snp | A/G | 0.249886 | 0.25 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828810 | AGGAGTTATTTGAAC[A/G]TCAGAAACAGTGATA | 5521 |
rs319150 | snp | C/T | 0.251014 | 0.249998 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828105 | CTGCTCCTAACCTCC[C/T]TGAGTTGCAACTATT | 5521 |
rs319151 | snp | A/G | 0.490343 | 0.0688145 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146828057 | ACCATGAAAGAAAGC[A/G]TACATGATTGTCTGT | 5521 |
rs319152 | snp | A/G | 0.490287 | 0.0690083 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146827893 | GTGTAGGAAGACGAC[A/G]GAAAAAGGGCTTAAT | 5521 |
rs319153 | snp | A/G | 0.199873 | 0.244923 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840875 | TATCAGATTAAGGAC[A/G]TGTTTGTTTCTTTTA | 5521 |
rs319154 | snp | A/G | 0.493568 | 0.0563433 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840194 | GGCAGCAATTGACAA[A/G]CCTGCATTTGAACCC | 5521 |
rs319155 | snp | A/T | 0.181659 | 0.240478 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146840041 | GCTCAGCTACACAAG[A/T]CTCAAGTTTTCAACA | 5521 |
rs319156 | snp | A/G | 0.493107 | 0.0583 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146925383 | tatccttcaaaaatg[A/G]gggcaaaataaggac | 5521 |
rs319157 | snp | A/T | 0.0425829 | 0.139564 | intron-variant | PPP2R2B | GRCh38.p7 | 5:146924658 | caggatggtgaaagc[A/T]gatcataaacctaaa | 5521 |
rs319158 | snp | C/T | 0.0433465 | 0.140692 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921188 | TATTAATTAGCACTT[C/T]ATGGGGTTTTTCAAA | 5521 |
rs319159 | snp | A/G | 0.386313 | 0.209568 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921043 | TGAAGAACAAAGACC[A/G]GAGACAACATACTGT | 5521 |
rs319160 | snp | A/G | 0.481703 | 0.0938806 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146921008 | TGCACCCTAGAAAAG[A/G]CTAATTTGGTCTGCC | 5521 |
rs319161 | snp | A/G | 0.485664 | 0.0834419 | intron-variant, upstream-variant-2KB | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146920591 | GACTGGCAGTCATGA[A/G]GTTATGTAGCAAAGA | 5521 |
rs319162 | snp | G/T | 0.402454 | 0.198136 | intron-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146919058 | ctaggaaatgggaaC[G/T]TTCATATATAGGTTT | 5521 |
rs319163 | snp | A/G | 0.0566069 | 0.158427 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146917478 | GATAGACACCAATGA[A/G]CAGAATAAACATTTT | 5521 |
rs319164 | snp | C/T | 0.0429648 | 0.14013 | intron-variant, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146915646 | GTCGTTAAGGAAATA[C/T]TATGTTTCTTTCTCT | 5521 |
rs319165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B, nc-transcript-variant | PPP2R2B, PPP2R2B-IT1, LOC105378214 | GRCh38.p7 | 5:146913711 | TATGGTATTAGAGAG[C/T]GTTCCTCAAATTTTG | 5521 |