| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs582142 | snp | A/G | 0.219049 | 0.248077 | intron-variant | RNF212 | GRCh38.p7 | 4:1095185 | TGATGAGCCAGGTGC[A/G]CTATCCCGAGACCAT | 285498 |
| rs582202 | snp | C/T | 0.334642 | 0.235236 | intron-variant | RNF212 | GRCh38.p7 | 4:1095155 | TGGAGCTGTGGGGGG[C/T]GTGCTTGGTTCTGTG | 285498 |
| rs583100 | snp | A/G | 0.290977 | 0.246619 | intron-variant | RNF212 | GRCh38.p7 | 4:1088398 | gccaggtcacatctt[A/G]aacgctttgctgctt | 285498 |
| rs584472 | snp | C/G | 0.285257 | 0.247501 | intron-variant | RNF212 | GRCh38.p7 | 4:1094686 | CAGGGCCTTCTGCCT[C/G]CCAGGCCTCCAATCC | 285498 |
| rs585735 | snp | C/G | 0.350546 | 0.22889 | intron-variant | RNF212 | GRCh38.p7 | 4:1086603 | CTCACCCCCACCCCT[C/G]TCCTGCCACCCTCAT | 285498 |
| rs588824 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1099171 | ACATTGCAGAGGGCC[A/G]GCGATAAGCCAGGTG | 285498 |
| rs589660 | snp | G/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1099312 | CTAACAGCCCAGCAC[G/T]AAAATAAATAATAAA | 285498 |
| rs590118 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | RNF212 | GRCh38.p7 | 4:1099437 | TCTAAGTGAGTATTA[A/G]CTGTCCATGGCAGCA | 285498 |
| rs604526 | snp | C/T | 0.281841 | 0.247964 | intron-variant | RNF212 | GRCh38.p7 | 4:1092499 | GCCTCATGCCGCCTC[C/T]GTGGTTTGTCTGGCC | 285498 |
| rs604597 | snp | A/G | 0.348134 | 0.229934 | intron-variant | RNF212 | GRCh38.p7 | 4:1100363 | ACTTCCGAGCTACTG[A/G]TGCACCTGTTACATT | 285498 |
| rs606293 | snp | A/G | 0.291493 | 0.246533 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092880 | GAGGCCAGGAGAGGC[A/G]GCTGCCTGGTCCGGA | 285498 |
| rs606327 | snp | A/G | 0.292266 | 0.246401 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092914 | CACTTCTCACTCTTC[A/G]GTTCAATACCAGTTC | 285498 |
| rs608066 | snp | A/G | 0.29175 | 0.246489 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093278 | gggttttatctgttg[A/G]tatttaccctattag | 285498 |
| rs610218 | snp | C/G | 0.346811 | 0.230494 | intron-variant | RNF212 | GRCh38.p7 | 4:1086295 | TGTGCCGTGGGATGA[C/G]CTGGCAGTGGCCGTG | 285498 |
| rs614945 | snp | G/T | 0.17481 | 0.238425 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093829 | CCAGCCAGAGGCCCA[G/T]GGAAACACCATCCAG | 285498 |
| rs615381 | snp | A/G | 0.176993 | 0.239102 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093743 | AGTCCCCTTGGGGCC[A/G]GAAGTTGCTTGAGTT | 285498 |
| rs616196 | snp | A/C | 0.170523 | 0.23703 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093605 | AGCAGACCCGGCCAG[A/C]CCCTCCAGCCACCTG | 285498 |
| rs616569 | snp | C/T | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1100126 | AAAAGAAGATGAAAT[C/T]AGTGTTGACAGCCGA | 285498 |
| rs617633 | snp | C/T | 0.274393 | 0.248807 | intron-variant | RNF212 | GRCh38.p7 | 4:1084092 | ATGTGTTGGTGCACA[C/T]CTGTAATCCCAGCTA | 285498 |
| rs619407 | snp | C/G | 0.290718 | 0.246662 | intron-variant | RNF212 | GRCh38.p7 | 4:1099470 | CTGGCTCTCACTGCA[C/G]GAGGCCCCACCATAC | 285498 |
| rs620398 | snp | A/G | 0.291493 | 0.246533 | intron-variant | RNF212 | GRCh38.p7 | 4:1099232 | TTCACAGACTTCAGA[A/G]TTCTTTGTTGAAAGT | 285498 |
| rs629260 | snp | C/T | 0.347914 | 0.230028 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092976 | TGGTCCTGGCGTAGT[C/T]TGGAGCTCATGTGGA | 285498 |
| rs629261 | snp | G/T | 0.347914 | 0.230028 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092975 | GGTCCTGGCGTAGTT[G/T]GGAGCTCATGTGGAC | 285498 |
| rs629638 | snp | C/G | 0.292266 | 0.246401 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092926 | CTCCATGGAGGAGAA[C/G]TGGTATTGAACCGAA | 285498 |
| rs630549 | snp | A/G | 0.292266 | 0.246401 | intron-variant | RNF212 | GRCh38.p7 | 4:1092715 | CTGACCTGGCCCAGC[A/G]CAGCCTCTGTGACCA | 285498 |
| rs632319 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098839 | ACAGTGACAGTTCCC[A/G]CTCCCTGCGCACTCA | 285498 |
| rs633087 | snp | A/G | 0.291493 | 0.246533 | intron-variant | RNF212 | GRCh38.p7 | 4:1098720 | TTCTGTTTTATACGT[A/G]GGGAGACCGAGGCAT | 285498 |
| rs633141 | snp | A/G | 0.291493 | 0.246533 | intron-variant | RNF212 | GRCh38.p7 | 4:1098690 | TGGTGGAGTTAGGTG[A/G]AGAACCAGGGTTGCA | 285498 |
| rs633556 | snp | C/T | 0.398534 | 0.201091 | intron-variant | RNF212 | GRCh38.p7 | 4:1098617 | TCCTGATGCCTGTGG[C/T]GTTGGACATACTGCT | 285498 |
| rs633599 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098576 | CAGTTTGGTGTGTAT[A/G]GGAGGGTGTTACACG | 285498 |
| rs633954 | snp | C/T | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1094484 | AGAGAATGGACAAGC[C/T]GCAACTGAGAGGACT | 285498 |
| rs636976 | snp | A/G | 0.291493 | 0.246533 | intron-variant | RNF212 | GRCh38.p7 | 4:1095127 | TGGTCTCAGGATAGC[A/G]CACCTGGCTCATCAC | 285498 |
| rs641987 | snp | A/G | 0.350327 | 0.228986 | intron-variant | RNF212 | GRCh38.p7 | 4:1083754 | GCTGTGATCTCCGTC[A/G]TCTTAGGCCACCTGG | 285498 |
| rs643043 | snp | A/G | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1092146 | ACATGTGAAGCTGAG[A/G]AGCAGAGGCGCTTGC | 285498 |
| rs643484 | snp | C/T | 0.347032 | 0.230401 | intron-variant | RNF212 | GRCh38.p7 | 4:1092038 | GGCGTGTGCAGGTGT[C/T]CCCGACAGGCAGCAG | 285498 |
| rs646117 | snp | C/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098041 | GTCTTGCTCTGTTGC[C/G]CAGGCTGGAGTGCAG | 285498 |
| rs647828 | snp | C/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1097702 | CTAATGTGGTCCTGG[C/G]TGGGGAAAGTGAGGG | 285498 |
| rs648640 | snp | A/G | 0.0208471 | 0.0999448 | intron-variant | RNF212 | GRCh38.p7 | 4:1096714 | GCTCCATGGTCTCGG[A/G]ATAGTGCACCTGGCT | 285498 |
| rs649243 | snp | A/G | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1090977 | GCACTGGCCATGGGC[A/G]TCTGTGGGGGCAGGA | 285498 |
| rs649258 | snp | A/G | 0.295599 | 0.245806 | intron-variant | RNF212 | GRCh38.p7 | 4:1097375 | ccttgtgatccgccc[A/G]cctcggcctcccaaa | 285498 |
| rs649616 | snp | A/G | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1097319 | ccgctcccgaccTAC[A/G]AGACGCTGTTTCTTA | 285498 |
| rs649950 | snp | A/G | 0.278399 | 0.248382 | intron-variant | RNF212 | GRCh38.p7 | 4:1096998 | GCCAGGGACAGCCTC[A/G]ATCAACAGGACAGCC | 285498 |
| rs651017 | snp | A/G | 0.401037 | 0.199218 | intron-variant | RNF212 | GRCh38.p7 | 4:1097274 | TTATTTAAAAAGCAA[A/G]TGTAAGGACCTTAAG | 285498 |
| rs651135 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1090543 | GCATGGGCCTCCCTG[C/T]CTGGCCACACTTATC | 285498 |
| rs651509 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1090515 | ATCCCCTCAGCCACC[C/T]GGGGCAACACTGGGG | 285498 |
| rs652063 | snp | A/G | 0.347253 | 0.230308 | intron-variant | RNF212 | GRCh38.p7 | 4:1090349 | TGGGGCCGCTTCCCC[A/G]AGTCTGGAAGCCAGC | 285498 |
| rs658320 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1091059 | GAATGGAGCAGGTTG[C/T]TGGGGAGACTTTCCT | 285498 |
| rs658846 | snp | C/G | 0.27223 | 0.24966 | intron-variant | RNF212 | GRCh38.p7 | 4:1090935 | CAAGCACTGTGAGCT[C/G]TCCTGAGAGTCCCTC | 285498 |
| rs661364 | snp | G/T | 0.292951 | 0.250548 | intron-variant | RNF212 | GRCh38.p7 | 4:1096974 | CCCTGGCAGGGCCCC[G/T]GAGAGGCCATTCACA | 285498 |
| rs662667 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096697 | CGAGACCATGGAGCT[A/G]TGAGGGGTGTGCTTG | 285498 |
| rs662731 | snp | A/G | 0.208353 | 0.246507 | intron-variant | RNF212 | GRCh38.p7 | 4:1096635 | GACCATGGAGCTGTG[A/G]GGGGTGTGCTTGGTT | 285498 |
| rs662732 | snp | A/G | 0.208353 | 0.246507 | intron-variant | RNF212 | GRCh38.p7 | 4:1096633 | CCATGGAGCTGTGAG[A/G]GGTGTGCTTGGTTCT | 285498 |
| rs671790 | snp | C/G | 0.268724 | 0.249298 | intron-variant | RNF212 | GRCh38.p7 | 4:1083097 | CTCTCTACATACCTG[C/G]TATCGCCTGCATTTT | 285498 |
| rs674347 | snp | A/G | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1089797 | TAACAGCAGGAGAGA[A/G]GGCAGGGGGAACTGC | 285498 |
| rs676561 | snp | A/G | 0.347694 | 0.230122 | intron-variant | RNF212 | GRCh38.p7 | 4:1089324 | ccccatgcaagtcca[A/G]aacccagcagggcag | 285498 |
| rs681857 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098137 | AATGACAAGATGTAG[A/G]AAGAACCTCATGCCT | 285498 |
| rs682243 | snp | A/G | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098198 | GCATAGAGTCAAGAC[A/G]GTCATCTAAGCCCAT | 285498 |
| rs682787 | snp | C/T | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1098370 | TGGCTTGGATCAGGA[C/T]TAAGGCACCAGCTCC | 285498 |
| rs687939 | snp | G/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1089087 | ggcgtctggaggaca[G/T]tggccctcttctcat | 285498 |
| rs688008 | snp | A/G | 0.347694 | 0.230122 | intron-variant | RNF212 | GRCh38.p7 | 4:1089041 | caccccagttgggac[A/G]ctgtgtgggaacaac | 285498 |
| rs688785 | snp | C/G | 0.347473 | 0.230215 | intron-variant | RNF212 | GRCh38.p7 | 4:1088919 | ttccatacatcttct[C/G]aaatctaggtggagg | 285498 |
| rs689216 | snp | A/T | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1088825 | atgcttggggtttgc[A/T]ccctctgaagcagca | 285498 |
| rs935968 | snp | A/C | 0.405603 | 0.195673 | intron-variant | RNF212 | GRCh38.p7 | 4:1069399 | TACCTTTTGCCTCAT[A/C]CGGCCTCACCCCCCA | 285498 |
| rs935969 | snp | C/T | 0.366473 | 0.221211 | intron-variant | RNF212 | GRCh38.p7 | 4:1068800 | ccaatgaaattaaca[C/T]tttaaaatgaagact | 285498 |
| rs1010342 | snp | A/G | 0.367091 | 0.220884 | intron-variant | RNF212 | GRCh38.p7 | 4:1075031 | AAATCTCCGCAGAGC[A/G]TTCAAGTGCTGGTGT | 285498 |
| rs1383660 | snp | C/T | 0.293294 | 0.246223 | intron-variant | RNF212 | GRCh38.p7 | 4:1107428 | TCCTGGTCACTGTCA[C/T]CTCTGGGAAACAGGA | 285498 |
| rs1453605 | snp | A/G | 0.499575 | 0.0145705 | intron-variant | RNF212 | GRCh38.p7 | 4:1081983 | GATGATGGACATGAG[A/G]CACCATGGCTGGCCT | 285498 |
| rs1466214 | snp | A/G | 0.481242 | 0.0950111 | intron-variant | RNF212 | GRCh38.p7 | 4:1079972 | AGGGAGAAGCTGAGT[A/G]TGCAGAGGTGCAAGA | 285498 |
| rs1466215 | snp | A/G | 0.49889 | 0.0235361 | intron-variant | RNF212 | GRCh38.p7 | 4:1078432 | CCGTCGTCTGTCCTG[A/G]TGGGCAGAACTCAGC | 285498 |
| rs1466216 | snp | C/T | 0.440609 | 0.161766 | intron-variant | RNF212 | GRCh38.p7 | 4:1078119 | AGCCCTTTATAGATA[C/T]GAACTCAGTCGTGTA | 285498 |
| rs1670533 | snp | C/T | 0.350546 | 0.22889 | RNF212 | 4 | allele_origin=T(germline)/C(germline) | 4:1084399 | ATGGCTTTTACATTT[C/T]TAGAAGATTGTAAAC | 285498 |
| rs1670534 | snp | A/G | 0.375258 | 0.216357 | intron-variant, missense | RNF212 | GRCh38.p7 | 4:1093477 | ACTGTGGAGGTGAGC[A/G]TCACAAACGCAGGGT | 285498 |
| rs1680026 | snp | A/G | 0.292523 | 0.246357 | intron-variant | RNF212 | GRCh38.p7 | 4:1092801 | GCGAACTGGGAGGCC[A/G]AGAAGGCCTGAGAGT | 285498 |
| rs1680027 | snp | A/C | 0.292523 | 0.246357 | intron-variant | RNF212 | GRCh38.p7 | 4:1092802 | CGAACTGGGAGGCCG[A/C]GAAGGCCTGAGAGTC | 285498 |
| rs1825092 | snp | A/G | 0.292523 | 0.246357 | intron-variant | RNF212 | GRCh38.p7 | 4:1107121 | cagtggtgtgatctc[A/G]gctcaccacagcctc | 285498 |
| rs1825093 | snp | A/G | 0.49614 | 0.0437598 | intron-variant | RNF212 | GRCh38.p7 | 4:1107294 | ctgacctcatgatcc[A/G]cctgcctcagcctcc | 285498 |
| rs2014318 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1074990 | GTCCCTTCGAACTAC[A/G]TTCCATTTGCTGCTC | 285498 |
| rs2045065 | snp | C/T | 0.347032 | 0.230401 | intron-variant | RNF212 | GRCh38.p7 | 4:1058700 | TTGCTATCCAGCTGC[C/T]GATGATTCAGATGGC | 285498 |
| rs2045066 | snp | A/G | 0.361894 | 0.223562 | intron-variant | RNF212 | GRCh38.p7 | 4:1058613 | TATTTACGCCCTCAT[A/G]TGGAAGACCCAGGGC | 285498 |
| rs2045067 | snp | A/G | 0.350327 | 0.228986 | intron-variant | RNF212 | GRCh38.p7 | 4:1058567 | GTTGGCACCAGGGCT[A/G]CCCGCAACCTAAGAG | 285498 |
| rs2045068 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1058424 | ATGTGTTAACATGAA[C/T]GACTCATGTTTTATT | 285498 |
| rs2045069 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1058418 | TAACATGAACGACTC[A/G]TGTTTTATTCTTGTT | 285498 |
| rs2100411 | snp | A/G | 0.350109 | 0.229081 | intron-variant | RNF212 | GRCh38.p7 | 4:1080624 | ggcaggtttcccgtg[A/G]ggagttttaattggt | 285498 |
| rs2248083 | snp | G/T | 0.346811 | 0.230494 | missense, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1058378 | GCAGCGTCTCCTCCC[G/T]GGGCCCCGAGCATCC | 285498 |
| rs2290407 | snp | A/G | 0.254498 | 0.24996 | intron-variant | RNF212 | GRCh38.p7 | 4:1081483 | GACGCTGGCATTTTC[A/G]TCATCACTCTTCCAG | 285498 |
| rs2290408 | snp | A/C | 0.347473 | 0.230215 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073479 | TGCTGTCCTTCCACC[A/C]GGTGCATGGGAGGCT | 285498 |
| rs2290409 | snp | A/G | 0.498813 | 0.0243321 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073461 | TGCATGGGAGGCTAC[A/G]TATTCACCAAAATGG | 285498 |
| rs2290410 | snp | A/T | 0.363776 | 0.222609 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058290 | AAGCACCTTCTTCAC[A/T]GCGTTCTAACCCCCG | 285498 |
| rs2290411 | snp | A/G | 0.350982 | 0.228698 | intron-variant | RNF212 | GRCh38.p7 | 4:1057289 | GCTTTTGATGCCTGC[A/G]GTCCAGTCCACCCCT | 285498 |
| rs2924495 | snp | C/T | 0.291235 | 0.246576 | intron-variant | RNF212 | GRCh38.p7 | 4:1097713 | AGTGTTTTGTGCTAA[C/T]GTGGTCCTGGCTGGG | 285498 |
| rs2932768 | snp | A/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067806 | ccaggagtcggaggt[A/T]gcagtgagccgagat | 285498 |
| rs3199881 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1101018 | GAAATTACAGACAGG[A/G]GTTTTAACATTGTGG | 285498 |
| rs3221827 | microsatellite | (CA)11/12/17/18/19/20/21/22 | 0.786708 | 0.124735 | intron-variant | RNF212 | GRCh38.p7 | 4:1106251 | AAACAATTTTACTTA[(CA)11/12/17/18/19/20/21/22]AGTCACTCAGACACA | 285498 |
| rs3796619 | snp | C/T | 0.498982 | 0.0225409 | RNF212 | 4 | allele_origin=T(germline)/C(germline) | 4:1101493 | CAGGTGGCAGAGTCA[C/T]AATCCTTCAACAGGA | 285498 |
| rs3796620 | snp | C/T | 0.350546 | 0.22889 | intron-variant | RNF212 | GRCh38.p7 | 4:1101291 | AAAACAATACAATTA[C/T]GGAAAATCAGTGAAA | 285498 |
| rs3816474 | snp | C/T | 0.275197 | 0.248727 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056865 | CCGCCCATCAGCATC[C/T]CCAGCCTGCTGCAGA | 285498 |
| rs4045481 | snp | A/G | 0.46341 | 0.130216 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1096837 | CTGGATATCTGCGTC[A/G]GTCTGAAAGAGAAAG | 285498 |
| rs4045482 | in-del | -/GA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1098189 | CAGTGAGCGCATAGA[-/GA]GTCAAGACGGTCATC | 285498 |
| rs4246683 | snp | A/G | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1110215 | CTCACTAGTCAATTA[A/G]AAAGAAACACCTCAA | 285498 |
| rs4246684 | snp | A/G | 0.293294 | 0.246223 | intron-variant | RNF212 | GRCh38.p7 | 4:1110416 | GGTCGCATTTGGGTC[A/G]GTTTTCATGTGCACA | 285498 |
| rs4690209 | snp | C/T | 0.498206 | 0.0298983 | intron-variant | RNF212 | GRCh38.p7 | 4:1083787 | ACCTGCAGCTCCCCA[C/T]CCTCGACGTCAGCCT | 285498 |
| rs4690210 | snp | A/G | 0.428937 | 0.17459 | intron-variant | RNF212 | GRCh38.p7 | 4:1070567 | ACAGCACAGTCCTAC[A/G]AAACCACCTGTAACT | 285498 |
| rs4690211 | snp | C/T | 0.375 | 0.216506 | intron-variant | RNF212 | GRCh38.p7 | 4:1070558 | TCCTACAAAACCACC[C/T]GTAACTCAGGCCAGG | 285498 |
| rs4690212 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1061110 | GTCCCGCTCCTCCCA[A/G]AGCTGCAACGGGATT | 285498 |
| rs4690213 | snp | A/G | 0.368119 | 0.220336 | intron-variant | RNF212 | GRCh38.p7 | 4:1061080 | TTCAGGAGTCAGTGT[A/G]TTCTGATTTCAGGAG | 285498 |
| rs4690214 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1060848 | AGTGGCAGGCGGGCC[A/G]TCTGTGCGTTGTCTG | 285498 |
| rs4690215 | snp | C/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1060831 | CTGTGCGTTGTCTGC[C/G]CTGCAGACTCACTGA | 285498 |
| rs4690343 | snp | A/G | 0.35445 | 0.227135 | intron-variant | RNF212 | GRCh38.p7 | 4:1063788 | ctcctgggctcaatc[A/G]atcctcccacctcag | 285498 |
| rs4690344 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1063671 | gtctcactctgttgc[C/T]caagctggagtgcaa | 285498 |
| rs4690345 | snp | C/G | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1063591 | gcctcagcctcctga[C/G]gagctgggattacag | 285498 |
| rs4690346 | snp | A/G | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1063569 | ggattacaggtgcgc[A/G]ccaccacacctggct | 285498 |
| rs4690347 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1063540 | ctagttttgtagaga[C/T]ggggtttcaccatgt | 285498 |
| rs4974561 | snp | A/C | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1103545 | tacaagctaccttgt[A/C]tcactacaaagttga | 285498 |
| rs4974569 | snp | C/T | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1109573 | CAGACTTGAGGATTC[C/T]AACGCTGCTGAGTCA | 285498 |
| rs4974571 | snp | A/C | 0.293294 | 0.246223 | intron-variant | RNF212 | GRCh38.p7 | 4:1109686 | TCATCTACTCAGAAG[A/C]AGCCCTGGCTCATGA | 285498 |
| rs4974573 | snp | C/T | 0.283158 | 0.247791 | intron-variant | RNF212 | GRCh38.p7 | 4:1110809 | CACCCCTTTTCACCA[C/T]TTTTTTGTGTGTCTT | 285498 |
| rs4974601 | snp | A/G | 0.499 | 0.0223418 | intron-variant | RNF212 | GRCh38.p7 | 4:1101622 | AATTCCACACCACTC[A/G]TGACATCATCTGCTA | 285498 |
| rs4974628 | snp | A/G | 0.290718 | 0.246662 | intron-variant | RNF212 | GRCh38.p7 | 4:1103432 | ccaaaatgtggaaag[A/G]gcattacaagaaaaa | 285498 |
| rs4974637 | snp | C/T | 0.293807 | 0.246132 | intron-variant | RNF212 | GRCh38.p7 | 4:1105407 | CGGTGGTGCCCTATT[C/T]TGTGCGTTCAATCGT | 285498 |
| rs4974638 | snp | A/G | 0.497151 | 0.037632 | intron-variant | RNF212 | GRCh38.p7 | 4:1105413 | TGCCCTATTCTGTGC[A/G]TTCAATCGTAATGGA | 285498 |
| rs4974639 | snp | C/T | 0.29278 | 0.246313 | intron-variant | RNF212 | GRCh38.p7 | 4:1105579 | CTGGGGAAGTCCACT[C/T]ACAATGTGTTTTGTT | 285498 |
| rs4974642 | snp | C/G | 0.283158 | 0.247791 | intron-variant | RNF212 | GRCh38.p7 | 4:1107824 | TTATGTTTGTAATCA[C/G]AAAAAAACAACTATT | 285498 |
| rs4974643 | snp | G/T | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1107969 | CATTGTTTTAAGCCT[G/T]CAGCAGTAATTGATT | 285498 |
| rs4974644 | snp | C/T | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1108262 | AAATTTTAGACACCA[C/T]AAATGACTAAAAATT | 285498 |
| rs5855685 | in-del | -/G | 0.350327 | 0.228986 | intron-variant | RNF212 | GRCh38.p7 | 4:1074916 | CATCCTAGCGGATGG[-/G]AAGGATCCAGAAATG | 285498 |
| rs6599276 | snp | C/T | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1063039 | aactgcaaaataccg[C/T]tgaaagaaatcaaag | 285498 |
| rs6599278 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1065010 | tcatagcccactgta[C/T]ggagacacacattgt | 285498 |
| rs6599279 | snp | A/G | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1065045 | atccattcatctgat[A/G]gatacttagatggct | 285498 |
| rs6599280 | snp | A/G | 0.348134 | 0.229934 | intron-variant | RNF212 | GRCh38.p7 | 4:1070030 | CCTGGCCTGAGTTAC[A/G]GGTGGTTTCGTAGGA | 285498 |
| rs6599282 | snp | A/G | 0.222928 | 0.24853 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114619 | TTCAATGTGGAGACT[A/G]GAAAACTTAGAATTA | 285498 |
| rs6599283 | snp | C/T | 0.223522 | 0.248594 | upstream-variant-2KB, intron-variant | RNF212, TMED11P, LOC105374344 | GRCh38.p7 | 4:1115148 | ATAATGATATAACGT[C/T]AATCTCAATCTCTGG | 285498 |
| rs6812586 | snp | A/G | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1076063 | CCTGGTCAATTTTAC[A/G]TAATAGAAAATGCCA | 285498 |
| rs6812596 | snp | A/G | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1076078 | ATAATAGAAAATGCC[A/G]TGCTCATTTAAGGTT | 285498 |
| rs6814094 | snp | C/T | 0.290977 | 0.246619 | intron-variant | RNF212 | GRCh38.p7 | 4:1102477 | acacacagttaaaac[C/T]tgtgttgttcaagag | 285498 |
| rs6814276 | snp | A/G | 0.272241 | 0.249009 | intron-variant | RNF212 | GRCh38.p7 | 4:1063665 | acaccattgcactcc[A/G]gcttgggcaacagag | 285498 |
| rs6814833 | snp | A/C | 0.350109 | 0.229081 | intron-variant | RNF212 | GRCh38.p7 | 4:1063891 | aaaaaaatgaaaaaa[A/C]CCAATATTAATAATA | 285498 |
| rs6817989 | snp | A/C | 0.27278 | 0.24896 | intron-variant | RNF212 | GRCh38.p7 | 4:1061019 | AAACAACCATTCAGG[A/C]CTCTGGAAATCAATT | 285498 |
| rs6820779 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | RNF212 | GRCh38.p7 | 4:1104127 | gcagtccaaatcatt[A/G]aatacctaACAGAGA | 285498 |
| rs6821725 | snp | C/G | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1066572 | ctgagctcaagcgat[C/G]cttttgccttggtct | 285498 |
| rs6822863 | snp | A/G | 0.367913 | 0.220446 | intron-variant | RNF212 | GRCh38.p7 | 4:1061818 | caatcaaacaacctt[A/G]gataaaaatacaaga | 285498 |
| rs6827206 | snp | A/T | 0.347473 | 0.230215 | downstream-variant-500B, intron-variant | RNF212 | GRCh38.p7 | 4:1071283 | aCTAACTTGGTTTTT[A/T]AAATACTATTCTTAC | 285498 |
| rs6827357 | snp | A/C | 0.366885 | 0.220993 | intron-variant | RNF212 | GRCh38.p7 | 4:1065414 | AAAATACTTTGAGGA[A/C]AGCTGCATCCACAGA | 285498 |
| rs6827376 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1065435 | CATCCACAGACTTCA[A/G]CTATGTGATTACTTC | 285498 |
| rs6831018 | snp | A/G | 0.331642 | 0.236293 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114172 | GCTGCACGCTTTGGG[A/G]CTAGTGTCCAGGTGG | 285498 |
| rs6833432 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | RNF212 | GRCh38.p7 | 4:1075527 | aactcacccaccatg[C/G]caaagacagcaccag | 285498 |
| rs6835141 | snp | G/T | 0.367503 | 0.220665 | intron-variant | RNF212 | GRCh38.p7 | 4:1076352 | CGCTGTCATGGGATG[G/T]CGCTGGCTTTGCTTC | 285498 |
| rs6835418 | snp | C/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1069204 | caacagagcaagatt[C/G]tgtctcaaaaaaaaa | 285498 |
| rs6836350 | snp | C/T | 0.367297 | 0.220775 | intron-variant | RNF212 | GRCh38.p7 | 4:1076185 | TCTCCCTTGCCTTCC[C/T]GGGCACCTTGTCCAG | 285498 |
| rs6837145 | snp | C/T | 0.365232 | 0.22186 | intron-variant | RNF212 | GRCh38.p7 | 4:1077279 | gacagaaaaTGCCCA[C/T]GTCTGGTCTTTGCCC | 285498 |
| rs6839147 | snp | A/G | 0.29432 | 0.24604 | intron-variant | RNF212 | GRCh38.p7 | 4:1102579 | acaaaaaTACAAAAA[A/G]AAAACACAAAAAAAC | 285498 |
| rs6839291 | snp | A/C | 0.294064 | 0.246086 | intron-variant | RNF212 | GRCh38.p7 | 4:1102583 | aaaTACAAAAAAAAA[A/C]CACAAAAAAACAAAA | 285498 |
| rs6839768 | snp | C/G | 0.29175 | 0.246489 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111676 | ATCTACTTTTCACCT[C/G]GCTGCCCGAGACACT | 285498 |
| rs6839931 | snp | C/T | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1059384 | CTGCCTTCACTTCTG[C/T]CTTGTATCACGGTTT | 285498 |
| rs6840162 | snp | A/G | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1103066 | CCACTGTTaaacaag[A/G]ggcatcattatggaa | 285498 |
| rs6840347 | snp | C/T | 0.280256 | 0.248162 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111892 | atccatacaatggaa[C/T]accacacaacaatga | 285498 |
| rs6845252 | snp | G/T | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1102899 | gtaatcccagcactt[G/T]gggaggccgaggcgg | 285498 |
| rs6845701 | snp | A/G | 0.488545 | 0.074807 | intron-variant | RNF212 | GRCh38.p7 | 4:1079211 | ATGGGACCAACATAG[A/G]GTCAACACAGGACCA | 285498 |
| rs6850784 | snp | A/G | 0.368119 | 0.220336 | intron-variant | RNF212 | GRCh38.p7 | 4:1066021 | taggactacaggtgc[A/G]attttttaaatatat | 285498 |
| rs6850869 | snp | C/T | 0.488545 | 0.074807 | intron-variant | RNF212 | GRCh38.p7 | 4:1079208 | AACATGGGACCAACA[C/T]AGAGTCAACACAGGA | 285498 |
| rs6851243 | snp | A/C | 0.375 | 0.216506 | intron-variant | RNF212 | GRCh38.p7 | 4:1065539 | gtggtatgatcactg[A/C]tcactgcagccttga | 285498 |
| rs6852155 | snp | G/T | 0.35445 | 0.227135 | intron-variant | RNF212 | GRCh38.p7 | 4:1073850 | TGCTGGTGGTAGAGG[G/T]GGTGTGGGTGGGTAT | 285498 |
| rs6852246 | snp | A/C | 0.271432 | 0.24908 | intron-variant | RNF212 | GRCh38.p7 | 4:1058768 | AGCCTCACTGAGGGG[A/C]CCTCGGCCCGTGGGC | 285498 |
| rs6852558 | snp | C/T | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1066156 | tccatctccttggct[C/T]gagcaatcctcccac | 285498 |
| rs6852850 | snp | C/G | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1059069 | CCCCAGGATGGGAAA[C/G]CCACCCAGTGAGGGA | 285498 |
| rs6852968 | snp | C/T | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1066371 | tctcacactgtcacc[C/T]aggctggagtgcagt | 285498 |
| rs6853838 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083663 | aaacaaacaaacaaa[C/T]aaacaaacaaacTCA | 285498 |
| rs6854793 | snp | C/T | 0.368119 | 0.220336 | intron-variant | RNF212 | GRCh38.p7 | 4:1061980 | ggcccagatcgcatt[C/T]cctaaggactccaga | 285498 |
| rs6857085 | snp | A/C | 0.345704 | 0.230956 | intron-variant | RNF212 | GRCh38.p7 | 4:1102132 | AGGTTGAAAATTAAT[A/C]CTAAGCACCCATCTT | 285498 |
| rs6858612 | snp | C/T | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1059565 | GTTCCACTCACCCTG[C/T]CTGATCCTCCCATGA | 285498 |
| rs7660109 | snp | A/G | 0.0930568 | 0.194599 | upstream-variant-2KB, intron-variant | RNF212, TMED11P, LOC105374344 | GRCh38.p7 | 4:1115425 | CTATGCGGAAAAGAA[A/G]TAGGTTTAGTGTCAT | 285498 |
| rs7660779 | snp | A/G | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1082152 | GAAGGGGAAAGGGAA[A/G]GGAAAGAAAAGAGAA | 285498 |
| rs7669399 | snp | G/T | 0.367913 | 0.220446 | intron-variant | RNF212 | GRCh38.p7 | 4:1064690 | ttttcagtgtacagt[G/T]cactggtattaaata | 285498 |
| rs7669622 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1064871 | tacgatcttgactac[C/T]tcacacacatggact | 285498 |
| rs7670185 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1095216 | CAGAACCAAGCACAC[C/T]CCCCACAGCTCCATG | 285498 |
| rs7673898 | snp | A/C | 0.34989 | 0.229177 | intron-variant | RNF212 | GRCh38.p7 | 4:1062781 | acaacctccacttgc[A/C]gatgacatgatttgc | 285498 |
| rs7679432 | snp | A/G | 0.350546 | 0.22889 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056733 | ACAACTCTTGAGAAC[A/G]TTTAGAGCTCCATGG | 285498 |
| rs7680608 | snp | C/G | 0.0513262 | 0.151752 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056649 | TTAAGTCATAATTTT[C/G]GAAATTCACAATGAA | 285498 |
| rs7685541 | snp | A/G | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1064713 | attaaatacattcct[A/G]atgctgtgcaaccat | 285498 |
| rs7685842 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1100237 | TCTTGTTTTGTGTTC[C/T]TGTCAAACATTCTGA | 285498 |
| rs7686048 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1100335 | ATGGTCCTTTTCACA[C/T]AGTGCACAGCTTACT | 285498 |
| rs7686397 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095237 | CAGCTCCATGGTCTC[A/G]GGATAGCGCACCTGG | 285498 |
| rs7686839 | snp | A/C | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1108787 | cactgcagccttgac[A/C]cccccgggctcaaca | 285498 |
| rs7687763 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1095217 | AGAACCAAGCACACT[C/T]CCCACAGCTCCATGG | 285498 |
| rs7691553 | snp | C/T | 0.293037 | 0.246268 | intron-variant | RNF212 | GRCh38.p7 | 4:1108730 | tgagacaaggtcttg[C/T]tctgttgcccaggct | 285498 |
| rs9762205 | snp | A/G | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1102628 | gaggctgaggcaggc[A/G]gatcacgaggtcagg | 285498 |
| rs9992322 | snp | A/G | 0.273587 | 0.248885 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073244 | TGGCCTGTGTGGGCT[A/G]AGGTGGATGTGTGCT | 285498 |
| rs9992925 | snp | A/T | 0.350546 | 0.22889 | intron-variant | RNF212 | GRCh38.p7 | 4:1057121 | AAAGGCATCTCTGAG[A/T]ACCTCGGAGCAGCAC | 285498 |
| rs9995279 | snp | C/T | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1057062 | TCTCTGGTGACACGG[C/T]AGTTACAGCACTGGC | 285498 |
| rs10003009 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1057061 | ATCTCTGGTGACACG[A/G]TAGTTACAGCACTGG | 285498 |
| rs10007978 | snp | A/T | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1067196 | gaggttagggcttca[A/T]catatgaattttggg | 285498 |
| rs10017931 | snp | A/G | 0.398174 | 0.201356 | intron-variant | RNF212 | GRCh38.p7 | 4:1066959 | gatccattttgaatt[A/G]acttttctacatagt | 285498 |
| rs10020875 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1067737 | ggtgaggtgctgcac[A/G/T]cctgtaattaatccc | 285498 |
| rs10026482 | snp | C/G | 0.350764 | 0.228794 | intron-variant | RNF212 | GRCh38.p7 | 4:1057340 | CTGACATGGGAGGGT[C/G]TGCCTTTTAGCGAGA | 285498 |
| rs10031302 | snp | A/G | 0.369346 | 0.219673 | intron-variant | RNF212 | GRCh38.p7 | 4:1065876 | cagacatccgtgccc[A/G]gccTGtttttgtttt | 285498 |
| rs10032349 | snp | A/G | 0.29278 | 0.246313 | intron-variant | RNF212 | GRCh38.p7 | 4:1104434 | TCTGCCCTGTTCTCC[A/G]GGGCTTCTGTGGTGA | 285498 |
| rs10032470 | snp | C/T | 0.292008 | 0.246445 | intron-variant | RNF212 | GRCh38.p7 | 4:1104381 | GTGGGTGGCCTTCCA[C/T]ACAGGCCCTGGGCTC | 285498 |
| rs10033163 | snp | A/G | 0.14665 | 0.227637 | intron-variant | RNF212 | GRCh38.p7 | 4:1101634 | CTCGTGACATCATCT[A/G]CTACATCGTCATCTA | 285498 |
| rs10049610 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112824 | TCCCCCTTCCCCCCC[A/C]AGCCTTGACCCCCCA | 285498 |
| rs10050240 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112827 | cccttcccccccaag[C/T]cttgaccccccacat | 285498 |
| rs10050241 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112837 | ccaagccttgacccc[C/T]cacatcccccacctt | 285498 |
| rs10084837 | snp | A/C | 0.494976 | 0.0498674 | intron-variant | RNF212 | GRCh38.p7 | 4:1060089 | GGGCAACAAGAGCGA[A/C]ACTCCATCAAAAAAA | 285498 |
| rs10084849 | snp | C/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1059798 | CTCAATACTATATGG[C/T]CAGTTGAAATTGTAG | 285498 |
| rs10084887 | snp | A/G | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1059866 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 285498 |
| rs10084888 | snp | G/T | 0.349013 | 0.229557 | intron-variant | RNF212 | GRCh38.p7 | 4:1060026 | TTGAACCTGGGAGGC[G/T]GAGGTTAGGTTGCAG | 285498 |
| rs10084889 | snp | A/G | 0.349013 | 0.229557 | intron-variant | RNF212 | GRCh38.p7 | 4:1060027 | TGAACCTGGGAGGCG[A/G]AGGTTAGGTTGCAGT | 285498 |
| rs10084890 | snp | C/G | 0.368938 | 0.219895 | intron-variant | RNF212 | GRCh38.p7 | 4:1060146 | CCTATTTACTCAATG[C/G]AAATTTTTCAAGATA | 285498 |
| rs10902752 | snp | C/T | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1062411 | gtaacagaacaaaac[C/T]caataatcatctcaa | 285498 |
| rs10902753 | snp | A/G | 0.368119 | 0.220336 | intron-variant | RNF212 | GRCh38.p7 | 4:1062435 | atctcaaaagagaaa[A/G]agaaagcacttgaaa | 285498 |
| rs11247971 | snp | A/G | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1059792 | CTTATGCTCAATACT[A/G]TATGGTCAGTTGAAA | 285498 |
| rs11247972 | snp | A/G | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1066762 | ttgcctttttactct[A/G]ttgatagtatctttt | 285498 |
| rs11247973 | snp | A/G | 0.495291 | 0.0482933 | intron-variant | RNF212 | GRCh38.p7 | 4:1100526 | GATTCTCTAGCCTCA[A/G]GCTCCCAAGTAATTG | 285498 |
| rs11510471 | snp | C/G | 0.484066 | 0.0878235 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113988 | GGGGCCCTGGGGGCC[C/G]GGGGAGCGGGATAGG | 285498 |
| rs11552885 | snp | A/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1101322 | TGCTGCTCAGTTTTT[A/T]TTGTCTACCAATGAT | 285498 |
| rs11723740 | snp | C/T | 0.00995 | 0.0698283 | intron-variant | RNF212 | GRCh38.p7 | 4:1091903 | TCCTGGGTGCCACCC[C/T]GTGGGCTATGAAGAG | 285498 |
| rs11724371 | snp | C/T | 0.341909 | 0.232492 | missense, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058337 | TGAGAGGCTTTCCCA[C/T]GCTCCTCTGACTCGT | 285498 |
| rs11724989 | snp | A/G | 0.290977 | 0.246619 | intron-variant | RNF212 | GRCh38.p7 | 4:1080648 | acctgcctggatgac[A/G]ccctgagccccaata | 285498 |
| rs11725984 | snp | C/T | 0.339145 | 0.233566 | intron-variant, synonymous-codon, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093550 | CTGTGACCTCCACGG[C/T]CCATGCCGGAAGCCT | 285498 |
| rs11726968 | snp | C/T | 0.279195 | 0.248289 | intron-variant | RNF212 | GRCh38.p7 | 4:1070039 | AGTTACAGGTGGTTT[C/T]GTAGGACTATGCTGT | 285498 |
| rs11727135 | snp | C/G | 0.350764 | 0.228794 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058015 | GCGGTGAGCCAAGAT[C/G]GTGCTACTGCACTCC | 285498 |
| rs11727136 | snp | A/G | 0.350764 | 0.228794 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058016 | CGGTGAGCCAAGATG[A/G]TGCTACTGCACTCCA | 285498 |
| rs11728360 | snp | A/G | 0.180666 | 0.240193 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113490 | CGACCGCAGCGGCGA[A/G]GCCGGGCCCACGCGA | 285498 |
| rs11731238 | snp | A/G | 0.275197 | 0.248727 | intron-variant | RNF212 | GRCh38.p7 | 4:1070045 | AGGTGGTTTCGTAGG[A/G]CTATGCTGTCAGCGT | 285498 |
| rs11731239 | snp | A/G | 0.279991 | 0.248195 | intron-variant | RNF212 | GRCh38.p7 | 4:1070048 | TGGTTTCGTAGGACT[A/G]TGCTGTCAGCGTGGA | 285498 |
| rs11731289 | snp | G/T | 0.349671 | 0.229272 | intron-variant | RNF212 | GRCh38.p7 | 4:1063985 | gtatcttcagtgaaa[G/T]tatccttcaaaatga | 285498 |
| rs11731320 | snp | A/T | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1064128 | AGATTTTTTTCCTCT[A/T]AAGGTCTTTAAGAAA | 285498 |
| rs11732259 | snp | A/G | 0.276534 | 0.248588 | intron-variant | RNF212 | GRCh38.p7 | 4:1070769 | atgctagggcaccac[A/G]tcggtaacatgctca | 285498 |
| rs11732520 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | RNF212 | GRCh38.p7 | 4:1080221 | GCCATCCTTATGGCT[C/T]GTGATCTCTGCGGAA | 285498 |
| rs11735663 | snp | C/T | 0.349671 | 0.229272 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058057 | CAAAGAGTGAGACTC[C/T]GGCTAAAAAAAAAAA | 285498 |
| rs11736950 | snp | C/T | 0.19646 | 0.2442 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113588 | AAAGTCGACGGCAGC[C/T]CTGCGCCCGCGCACT | 285498 |
| rs11938124 | snp | C/T | 0.380919 | 0.21298 | intron-variant | RNF212 | GRCh38.p7 | 4:1077064 | GAAACCAGGTCTCTA[C/T]TAAAAATACAAAAAT | 285498 |
| rs11939380 | snp | C/T | 0.49533 | 0.0480965 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093083 | CTGGGAAGAGGAAGA[C/T]GTTTAATTGTTACCA | 285498 |
| rs11940288 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1086040 | TTAAACCTTGAATCA[A/G]AATGTGGGTTACTCT | 285498 |
| rs11940546 | snp | C/T | 0.498871 | 0.0237351 | intron-variant | RNF212 | GRCh38.p7 | 4:1078697 | TGACACCAACAGAGA[C/T]TGACAGGGACCAGCA | 285498 |
| rs11940962 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | RNF212 | GRCh38.p7 | 4:1073834 | ACCTCCCGACTCTGC[C/G]TGCTGGTGGTAGAGG | 285498 |
| rs11947019 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1083592 | gaggtgagctgagat[C/T]gtgccactgtactcc | 285498 |
| rs11947960 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | RNF212 | GRCh38.p7 | 4:1059609 | GGTGCTAGGTCTCCC[C/T]TCACTCCCTCCCTGG | 285498 |
| rs12233733 | snp | C/T | 0.389715 | 0.207315 | intron-variant | RNF212 | GRCh38.p7 | 4:1064488 | cagaagtttatttct[C/T]gcagttctggagact | 285498 |
| rs12642550 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF212 | GRCh38.p7 | 4:1075497 | atgtacttttaacca[C/G]ccagatctcgtgaga | 285498 |
| rs12644468 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070541 | CTGTGTCAGCGTGGA[C/T]GCCTGGCCTGAGTTA | 285498 |
| rs12644767 | snp | A/C | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1065724 | cccaagtagctggga[A/C]tacaggtgtgtgcca | 285498 |
| rs12644880 | snp | C/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096331 | TCATCACGGAACCAA[C/G]CACACCCCCCACAGC | 285498 |
| rs12645289 | snp | C/T | 0 | 0 | downstream-variant-500B, intron-variant | RNF212 | GRCh38.p7 | 4:1071422 | Aaaactagaagaatt[C/T]tgttctgtgaaagat | 285498 |
| rs12645644 | snp | A/G | 0.368733 | 0.220005 | intron-variant | RNF212 | GRCh38.p7 | 4:1060371 | CAAGTCACACCAGGC[A/G]TCATCCTGAAGAGCA | 285498 |
| rs12646847 | snp | C/G | 0.375 | 0.216506 | intron-variant | RNF212 | GRCh38.p7 | 4:1096390 | TCATCACGGAACCAA[C/G]CACACCCCCCACAGC | 285498 |
| rs12647129 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095733 | CACCTGGCTCATCAC[A/G]GAACCAAGCACACCT | 285498 |
| rs12647792 | snp | A/C | 0.450357 | 0.149522 | intron-variant | RNF212 | GRCh38.p7 | 4:1095392 | ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAT | 285498 |
| rs12647929 | snp | G/T | 0.495708 | 0.0461266 | intron-variant | RNF212 | GRCh38.p7 | 4:1098231 | ACCTACCTACCAGTG[G/T]CTCCCCAAATCCCAC | 285498 |
| rs12650326 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070487 | GCTGTGTCAGCGTGG[A/G]TGCCTGGCCTGAGTT | 285498 |
| rs12650328 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070520 | GGGTGGTTTTGTAGG[A/G]CTGTGCTGTGTCAGC | 285498 |
| rs13106356 | snp | A/G | 0.437118 | 0.165792 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1094113 | GGCACAAGCCCATGA[A/G]GGAGAGTGCCATGCA | 285498 |
| rs13106586 | snp | A/G | 0.347914 | 0.230028 | intron-variant | RNF212 | GRCh38.p7 | 4:1060394 | GAAGAGCAGTAACTC[A/G]GAGAAAGGGGCCGCC | 285498 |
| rs13107058 | snp | A/G | 0.348794 | 0.229651 | intron-variant | RNF212 | GRCh38.p7 | 4:1060591 | AGCGCAGCGGTCTCC[A/G]TTCAGGGGAGTAATG | 285498 |
| rs13108207 | snp | C/T | 0.366679 | 0.221102 | intron-variant | RNF212 | GRCh38.p7 | 4:1060430 | TGCTAGAGGAAGGCC[C/T]GAAAGCCACCCAGAG | 285498 |
| rs13108222 | snp | A/C | 0.349013 | 0.229557 | intron-variant | RNF212 | GRCh38.p7 | 4:1060468 | AGCTCTCGAGAGCAC[A/C]GCAGCCCTGAGGTGG | 285498 |
| rs13108425 | snp | G/T | 0.00491398 | 0.0493238 | intron-variant | RNF212 | GRCh38.p7 | 4:1068418 | TTGATTTTTCAGCTG[G/T]GTTTTTAGAGTTATG | 285498 |
| rs13111842 | snp | C/T | | | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056087 | CGGCGCCGACCCACG[C/T]TGCGTGCGCACCCCA | 285498 |
| rs13114658 | snp | A/G | 0.444267 | 0.157354 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058221 | GACAATTTCCTTTAA[A/G]ACGCTGTGAAGAAGG | 285498 |
| rs13118024 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070593 | GCTGTGTCAGCGTGG[A/G]TGCCTGGCCTGAGTT | 285498 |
| rs13119276 | snp | C/T | 0.350546 | 0.22889 | intron-variant | RNF212 | GRCh38.p7 | 4:1057786 | AAGCAAACTCCTggc[C/T]gggcatggtggctca | 285498 |
| rs13119696 | snp | C/G | 0.295343 | 0.245854 | intron-variant | RNF212 | GRCh38.p7 | 4:1105009 | GCTCTCTTGTCTGCT[C/G]TCTCCAGGCCCTGGT | 285498 |
| rs13123326 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070524 | GGTTTTGTAGGGCTG[C/T]GCTGTGTCAGCGTGG | 285498 |
| rs13123543 | snp | A/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070603 | CGTGGATGCCTGGCC[A/T]GAGTTGTGGGTGGTT | 285498 |
| rs13134921 | snp | A/G | 0.347914 | 0.230028 | intron-variant | RNF212 | GRCh38.p7 | 4:1060389 | ATCCTGAAGAGCAGT[A/G]ACTCGGAGAAAGGGG | 285498 |
| rs13135215 | snp | A/G | 0.348354 | 0.22984 | intron-variant | RNF212 | GRCh38.p7 | 4:1060576 | CCCACAACATCTTCC[A/G]GCGCAGCGGTCTCCG | 285498 |
| rs13136494 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087519 | GGGGGGTGACAGGAT[A/G]AGGTGGGGGGGTGAC | 285498 |
| rs13137782 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | RNF212 | GRCh38.p7 | 4:1064570 | gccttctcactctgt[C/T]ttcatacggcctctt | 285498 |
| rs13140341 | snp | C/T | 0.348354 | 0.22984 | intron-variant | RNF212 | GRCh38.p7 | 4:1060447 | AAAGCCACCCAGAGC[C/T]AGGCCAGCTCTCGAG | 285498 |
| rs13140571 | snp | C/T | 0.346368 | 0.23068 | intron-variant | RNF212 | GRCh38.p7 | 4:1060570 | ACCATTCCCACAACA[C/T]CTTCCAGCGCAGCGG | 285498 |
| rs13141372 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070587 | GACTGTGCTGTGTCA[A/G]CGTGGATGCCTGGCC | 285498 |
| rs13141386 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070624 | GTGGGTGGTTTTGTA[A/G]GACTGCGCTGTGTCA | 285498 |
| rs13142697 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070548 | AGCGTGGACGCCTGG[C/T]CTGAGTTACAGGTGG | 285498 |
| rs13144566 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1089008 | tgctagggcagtgca[A/G]aagggaaatgtgcgg | 285498 |
| rs13146371 | snp | C/T | 0.480461 | 0.0968913 | intron-variant | RNF212 | GRCh38.p7 | 4:1089099 | ccactgtcctccaga[C/T]gccagaatggtagac | 285498 |
| rs13147452 | snp | A/G | 0.437542 | 0.165312 | intron-variant | RNF212 | GRCh38.p7 | 4:1084336 | gcaaagggctagcta[A/G]taaatgtaggaggct | 285498 |
| rs13435314 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | RNF212 | GRCh38.p7 | 4:1064346 | gttcaagatgcatgt[C/T]gtaatctctagagga | 285498 |
| rs17131824 | snp | C/G | 0.198324 | 0.244601 | intron-variant | RNF212 | GRCh38.p7 | 4:1057724 | CGTGGTACTTTTGAA[C/G]TTTTTAGCAACAGGG | 285498 |
| rs17164229 | snp | C/T | 0.278664 | 0.248351 | intron-variant | RNF212 | GRCh38.p7 | 4:1084808 | TTGGCCTGGAGTTTG[C/T]TTGCTGATGCCTGGA | 285498 |
| rs17164235 | snp | C/T | 0.279195 | 0.248289 | intron-variant | RNF212 | GRCh38.p7 | 4:1090273 | CAAGGGTGATCTGTC[C/T]GCTCCAGGTTTGGGT | 285498 |
| rs17164326 | snp | C/T | 0.285257 | 0.247501 | intron-variant | RNF212 | GRCh38.p7 | 4:1105749 | TATAAAGCGTCCTTC[C/T]ACCGCAGGTCAGGGT | 285498 |
| rs17728127 | snp | C/T | 0.0255323 | 0.11009 | missense, utr-variant-3-prime, intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1072981 | GGAACGGAAACAAGA[C/T]GGCCCTTTGTACCTC | 285498 |
| rs17729286 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | RNF212 | GRCh38.p7 | 4:1107360 | CTGGCCGAGAAGACA[A/C]CATTTTTATGAAAAG | 285498 |
| rs17795477 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1074043 | ACCTTGAAATCCAGA[A/T]GCTGATGGACAGGTT | 285498 |
| rs28374671 | snp | C/T | 0.295343 | 0.245854 | intron-variant | RNF212 | GRCh38.p7 | 4:1068240 | AAGTAACCAAGATAT[C/T]GTGGTATTTCTGAAA | 285498 |
| rs28478922 | snp | C/T | 0.217551 | 0.247885 | upstream-variant-2KB, intron-variant | RNF212, TMED11P, LOC105374344 | GRCh38.p7 | 4:1115523 | ATTAATATCTTACAC[C/T]AACGTATCCGTGCAG | 285498 |
| rs28481697 | snp | A/G | 0.210605 | 0.246877 | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056239 | GCAAACATATCACAT[A/G]TATGCTCGTCCTGAT | 285498 |
| rs28489841 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | RNF212 | GRCh38.p7 | 4:1099788 | TGGAGGAAATCAACC[C/T]TGGTGCAGAGCAATC | 285498 |
| rs28498761 | snp | A/G | 0.199254 | 0.244796 | intron-variant | RNF212 | GRCh38.p7 | 4:1060773 | TACTGAAGAGTGAGC[A/G]CCCTGCGCCCCTGCT | 285498 |
| rs28510738 | snp | C/G | 0.290977 | 0.246619 | intron-variant | RNF212 | GRCh38.p7 | 4:1091183 | AGGTGTGGACCAATG[C/G]CTGGGGCAAGTGGAA | 285498 |
| rs28514301 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1091096 | CGAGTGGTGCTCTAC[C/T]GCTGGGCCAATCACA | 285498 |
| rs28515819 | snp | A/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1099586 | TTTTGTTAGACTTTT[A/T]AAAGTCAAGATTGCT | 285498 |
| rs28537704 | snp | C/T | 0.426354 | 0.177198 | intron-variant | RNF212 | GRCh38.p7 | 4:1095394 | AGAACCAAGCACACC[C/T]CCCACAGCTCCATGG | 285498 |
| rs28562028 | snp | A/G | 0.350109 | 0.229081 | intron-variant | RNF212 | GRCh38.p7 | 4:1061327 | AGGTGGGAGGGGAAC[A/G]CTTTCATCAGCCACG | 285498 |
| rs28566546 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1100382 | ACCTGTTACATTTCC[A/C]CAGGCATTTTCCATA | 285498 |
| rs28579427 | snp | A/G | 0.270351 | 0.24917 | intron-variant | RNF212 | GRCh38.p7 | 4:1068493 | TTGCTCCATCTCCTC[A/G]CTCTTCCTTTGTGCT | 285498 |
| rs28588234 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1091132 | CTGTCCCTCTGATAA[C/T]GGCTACTGGTTTGAG | 285498 |
| rs28620427 | snp | G/T | 0.499053 | 0.0217445 | intron-variant | RNF212 | GRCh38.p7 | 4:1092459 | GCCTCCAGGACTCCA[G/T]TAGGGGGAGCCACAC | 285498 |
| rs28717061 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RNF212 | GRCh38.p7 | 4:1084384 | TCTCCGTTGCAATGC[A/G]TTTACAATCTTCTAG | 285498 |
| rs28720785 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056597 | TTTTAAAAAATTCAG[A/T]TGTCATCTTAGTATT | 285498 |
| rs28721561 | snp | A/C | 0.210605 | 0.246877 | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056246 | TATCACATGTATGCT[A/C]GTCCTGATAATCAGA | 285498 |
| rs33925889 | in-del | -/GA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1060114 | AAAAAAAAAAAAAAA[-/GA]AAAAAGAAATTGTTT | 285498 |
| rs33961572 | in-del | -/A | 0.387453 | 0.208822 | intron-variant | RNF212 | GRCh38.p7 | 4:1069210 | TCTCAAAAAAAAAAA[-/A]GAAATCTATGAATCC | 285498 |
| rs33984933 | in-del | -/C | 0.497907 | 0.0322805 | intron-variant | RNF212 | GRCh38.p7 | 4:1109750 | TGACCCACCACAGAA[-/C]AACCCACTTCACGCT | 285498 |
| rs33987054 | in-del | -/T | 0.296873 | 0.245566 | intron-variant | RNF212 | GRCh38.p7 | 4:1105301 | CCGCGCTCACCGGAG[-/T]CTCCCTTCCTGGCGG | 285498 |
| rs33995364 | in-del | -/G | 0.368324 | 0.220226 | intron-variant | RNF212 | GRCh38.p7 | 4:1059541 | GCCAACCCCAAGCCT[-/G]GGCGGCCTGTTCCAC | 285498 |
| rs33995683 | in-del | -/C | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1060555 | TGACCAGAGGGATAA[-/C]CCATTCCCACAACAT | 285498 |
| rs34094318 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083963 | TTTTTTTTTTTTTTT[-/T]GAGAGACGGAGTTTT | 285498 |
| rs34115363 | in-del | -/A | | | intron-variant | RNF212 | GRCh38.p7 | 4:1094801 | ACCTGAGATTCTAAC[-/A]GTGTGAATATGGGGA | 285498 |
| rs34169869 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112606 | GCCGCCTGCCCGCTT[-/T]CTCCCCCAGGTCCTC | 285498 |
| rs34243562 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070693 | GACTGTGCTGTGTCA[A/G]CGTGGGTGCCTGGCC | 285498 |
| rs34264311 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070461 | AGTTACGGGTGGTTT[C/T]GTAGGGCTGTGCTGT | 285498 |
| rs34341493 | in-del | -/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1069260 | TAAATTAGTGAATAC[-/C]ATAGATACCTGAATT | 285498 |
| rs34427379 | in-del | -/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1077796 | GCAGGGCCTGAGGGG[-/G]CAGGTGGGGTCCTCG | 285498 |
| rs34470931 | in-del | -/A | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1084750 | AAAAAAAAAAAAAAA[-/A]GCGAAGGAAAGGAAG | 285498 |
| rs34558698 | snp | A/G | 0.486332 | 0.08153 | intron-variant | RNF212 | GRCh38.p7 | 4:1079000 | ACACAGGACCAACAT[A/G]GGACCAACACAGGGT | 285498 |
| rs34559848 | in-del | -/T | | | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072402 | ATGTAAACCATGGAC[-/T]GTTGGGTGATAATGA | 285498 |
| rs34615470 | multinucleotide-polymorphism | GG/TA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1060026 | TTGAACCTGGGAGGC[GG/TA]AGGTTAGGTTGCAGT | 285498 |
| rs34624517 | in-del | -/A | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1102595 | AAAACACAAAAAAAC[-/A]AAAAAAAAACACTTT | 285498 |
| rs34688717 | snp | A/C | 0.0766824 | 0.180169 | intron-variant | RNF212 | GRCh38.p7 | 4:1067047 | CATTTCTCAAAAAAA[A/C]TGTCCTTTCCCCCAC | 285498 |
| rs34747195 | in-del | -/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1102184 | AAAAAGGAAATGATA[-/G]AAGAGAATTAACAAA | 285498 |
| rs34776143 | in-del | -/T | 0.28578 | 0.247426 | intron-variant | RNF212 | GRCh38.p7 | 4:1105745 | ATATAAAGCGTCCTT[-/T]CCACCGCAGGTCAGG | 285498 |
| rs34881651 | in-del | -/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1058814 | GCCCGTCACGGGGGC[-/C]AGCTGTGGGCATGCG | 285498 |
| rs35109101 | in-del | -/GT | | | intron-variant | RNF212 | GRCh38.p7 | 4:1106291 | ACACACACACACACA[-/GT]CACTCAGACACAGAG | 285498 |
| rs35166968 | in-del | -/CACACACACACACACA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1106275 | ACACACACACACACA[-/CACACACACACACACA]GTCACTCAGACACAG | 285498 |
| rs35223150 | snp | A/G | 0.469544 | 0.119585 | intron-variant | RNF212 | GRCh38.p7 | 4:1078956 | ACACAGGACCAACAC[A/G]GGACCAACATAGGAC | 285498 |
| rs35223974 | in-del | -/GA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1082149 | AGGAAGGGGAAAGGG[-/GA]AAGGGAAAGAAAAGA | 285498 |
| rs35299666 | in-del | -/CACA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1106287 | ACACACACACACACA[-/CACA]GTCACTCAGACACAG | 285498 |
| rs35322395 | in-del | -/A | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1103002 | CTACTAAAAAAATAC[-/A]AAAAAAAAAAAAATC | 285498 |
| rs35366709 | snp | C/T | 0.401215 | 0.199083 | intron-variant | RNF212 | GRCh38.p7 | 4:1107180 | CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG | 285498 |
| rs35409473 | in-del | -/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1100601 | TCAGTAGAGATGGGG[-/G]TTTCTCCTTGTTAGC | 285498 |
| rs35444175 | in-del | -/A | | | intron-variant | RNF212 | GRCh38.p7 | 4:1061914 | AGCAAAGAAACAGAA[-/A]GCGTGACCACACTCA | 285498 |
| rs35452482 | in-del | -/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1079288 | CAGGGTCAACACAAG[-/G]ACCAACATGGGACCA | 285498 |
| rs35484312 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1079369 | GAACAACACAGAACC[G/T]GCATGGGACCCTGCC | 285498 |
| rs35524911 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1097822 | TCATCCCAGCACTTT[-/T]GGGAGGCCAAGGTGG | 285498 |
| rs35538273 | in-del | -/T | 0.368119 | 0.220336 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072285 | GTGGCGCACAGAGGA[-/T]TTTTAGGGTGTGGCA | 285498 |
| rs35542476 | in-del | -/A | | | intron-variant | RNF212 | GRCh38.p7 | 4:1091363 | GCTTGAACTGGGTTT[-/A]CTGAGAGTACCAACA | 285498 |
| rs35564691 | in-del | -/A | 0.292266 | 0.246401 | intron-variant | RNF212 | GRCh38.p7 | 4:1092517 | GTTTGTCTGGCCTGG[-/A]CTCTGACCAATGTTG | 285498 |
| rs35755486 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070467 | GGGTGGTTTTGTAGG[A/G]CTGTGCTGTGTCAGC | 285498 |
| rs35807432 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1079879 | AGGGCCACCCGCCGT[-/T]CTGTACTGGGATGTA | 285498 |
| rs35917288 | in-del | -/A | | | intron-variant | RNF212 | GRCh38.p7 | 4:1088621 | GGACGGTGGAGAAAA[-/A]TGTCTCCAGGGCATG | 285498 |
| rs35950344 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1108881 | ATTTTTAAATTTTTT[-/T]GTAGAGACAGGGTCT | 285498 |
| rs36064454 | in-del | -/TT | 0.354881 | 0.226936 | intron-variant | RNF212 | GRCh38.p7 | 4:1064584 | TCTTCATACGGCCTC[-/TT]TTGTGTGTGTGCAGA | 285498 |
| rs55644007 | snp | A/C/G | 0.0948958 | 0.196212 | intron-variant | RNF212 | GRCh38.p7 | 4:1069657 | TCACCTCTGTGCTCC[A/C/G]ATGTGATGTGCTAAG | 285498 |
| rs55648209 | snp | C/T | 0.000379673 | 0.0137729 | intron-variant | RNF212 | GRCh38.p7 | 4:1081491 | GTGATGACGAAAATG[C/T]CAGCGTCAGTGCACA | 285498 |
| rs55649159 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070277 | TGTGTCAGCGTGGAC[A/G]CCTGGCCTGAGTTAC | 285498 |
| rs55676333 | snp | C/T | 0.093777 | 0.195178 | intron-variant | RNF212 | GRCh38.p7 | 4:1104765 | CCTTCCCTCGGGTCC[C/T]GATTTGGCCTGCAAT | 285498 |
| rs55741287 | snp | C/T | 0.480775 | 0.0961398 | intron-variant | RNF212 | GRCh38.p7 | 4:1100882 | AGAGGGCAGACGCTC[C/T]CATGTCACATGAGCA | 285498 |
| rs55741543 | snp | A/C | 0.00611615 | 0.0549606 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113601 | GCCCTGCGCCCGCGC[A/C]CTGGAGCTCGCGCCC | 285498 |
| rs55813847 | snp | C/T | 0.00167901 | 0.0289255 | synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073030 | TTTAGAGTTGGTGAG[C/T]TCCCCGTGCCTTCCA | 285498 |
| rs55829005 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095407 | ACTCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs55852307 | snp | C/G | 0.368119 | 0.220336 | intron-variant | RNF212 | GRCh38.p7 | 4:1066079 | CATCCTAATGAGATA[C/G]TATCTTGCTGTTTTT | 285498 |
| rs55943351 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1058789 | GCCCGTGGGCTCTGC[A/G]AGGGGAGCCTGCCCG | 285498 |
| rs56004360 | snp | A/G | 0.0622585 | 0.165085 | intron-variant | RNF212 | GRCh38.p7 | 4:1096559 | CACCTGGCTCATCAC[A/G]GAACCAAGCACAACT | 285498 |
| rs56019586 | snp | C/G | 0.349233 | 0.229462 | intron-variant | RNF212 | GRCh38.p7 | 4:1066054 | TAGCCATCCTAATGG[C/G]TGTTTATCTCATCCT | 285498 |
| rs56073221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1110154 | CAGAGAGGAAATCAC[A/G]TGCGGCCAAAAGACA | 285498 |
| rs56095683 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF212 | GRCh38.p7 | 4:1070382 | CTGTGTCAGCGTGGG[C/T]GCCTGGCCTGAGTTG | 285498 |
| rs56173468 | snp | C/T | 0.095934 | 0.196885 | intron-variant | RNF212 | GRCh38.p7 | 4:1111128 | TCCTCACTGGTCCAA[C/T]GGACACTTTCAAACA | 285498 |
| rs56213440 | snp | C/T | 0.357664 | 0.225629 | intron-variant | RNF212 | GRCh38.p7 | 4:1095453 | AGAACCAAGCACAAC[C/T]CCCACAGCTCCACGG | 285498 |
| rs56265368 | snp | A/G | 0.101658 | 0.201233 | intron-variant | RNF212 | GRCh38.p7 | 4:1089968 | GTATGAAGACAGACT[A/G]ATACAGGGTGACAGG | 285498 |
| rs56287616 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | RNF212 | GRCh38.p7 | 4:1108217 | ATTTTGATTACTCAG[A/G]TATCTTTGTTAACGG | 285498 |
| rs56294238 | snp | A/C | 0.354665 | 0.227036 | intron-variant | RNF212 | GRCh38.p7 | 4:1095451 | ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAC | 285498 |
| rs56311530 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096123 | AGCTCCACGGTCTCG[A/G]GATAGCGCACCTGGC | 285498 |
| rs56337816 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096351 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs56379835 | snp | A/G | 0.222616 | 0.248496 | intron-variant | RNF212 | GRCh38.p7 | 4:1096476 | CAGCTCCACGGTCTC[A/G]GGATAGTGCACCTGG | 285498 |
| rs56808305 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096410 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs56849878 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RNF212 | GRCh38.p7 | 4:1068473 | TCTCATCTTCTGCTC[C/T]ACTGTTGCTCCATCT | 285498 |
| rs56871016 | in-del | -/TTATCTCATCCTAAT | | | intron-variant | RNF212 | GRCh38.p7 | 4:1066058 | CATCCTAATGGCTGT[-/TTATCTCATCCTAAT]GAGATACTATCTTGC | 285498 |
| rs56889100 | snp | A/G | 0.108718 | 0.206251 | intron-variant, synonymous-codon, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093613 | TGGAGGGGCTGGCCG[A/G]GTCTGCTGGGTCTTC | 285498 |
| rs57094933 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1089282 | ATGTGAGACATTGGG[C/T]AAAAGGATAAATTTA | 285498 |
| rs57096673 | snp | C/T | 0.437259 | 0.165632 | intron-variant | RNF212 | GRCh38.p7 | 4:1095952 | ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs57186616 | snp | A/G | 0.240765 | 0.249829 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058312 | AAGGTGCTTGCGGGG[A/G]GGCACTACCTGAGAG | 285498 |
| rs57265466 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1105647 | GGGTACTGCACTAAG[C/T]GAGGATAAGAACTGC | 285498 |
| rs57280685 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | RNF212 | GRCh38.p7 | 4:1104818 | ACGTGTCTGCATCCT[C/T]GCCATGACCTGACAT | 285498 |
| rs57452522 | snp | C/G | | | synonymous-codon, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1058371 | CAGGCCGGGATGCTC[C/G]GGGCCCAGGGAGGAG | 285498 |
| rs57526991 | snp | A/C | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095687 | ACAGAACCAAGCACA[A/C]CTCCCACAGCTCCAT | 285498 |
| rs57677641 | snp | C/T | 0.0524618 | 0.153228 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093525 | GGGCCACGAGGTCAC[C/T]GGGCAGAGCCTGTGA | 285498 |
| rs57717353 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070398 | GCCTGGCCTGAGTTG[C/T]GGGTGGTTTTGTAGG | 285498 |
| rs57770549 | snp | A/G | 0.0217236 | 0.101931 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072602 | CCCAGTTAGAAAAAA[A/G]TGATTTAAGTATGTG | 285498 |
| rs57992451 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF212 | GRCh38.p7 | 4:1068455 | GTGGTTGCTTTAAAC[A/G]AGTCTCATCTTCTGC | 285498 |
| rs58088919 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1100425 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTAC | 285498 |
| rs58199323 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1111572 | TCATGTCTGCTGAAT[C/T]TACCTAACTTCTCCT | 285498 |
| rs58598469 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070434 | GCTGTGTCAGCGTGG[A/G]CGCCTGGCCTGAGTT | 285498 |
| rs58756267 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF212 | GRCh38.p7 | 4:1067854 | GCCTGGGCGACACAG[C/T]GAGACTCTGTCTCAA | 285498 |
| rs59057706 | snp | C/T | 0.197276 | 0.244377 | intron-variant, synonymous-codon, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093574 | GAAGCCTGAGAGGCA[C/T]GAGAGGCAGAGCAGA | 285498 |
| rs59378824 | in-del | -/AA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1084749 | AAAAAAAAAAAAAAA[-/AA]GCGAAGGAAAGGAAG | 285498 |
| rs59388255 | snp | A/G | 0.270351 | 0.24917 | intron-variant | RNF212 | GRCh38.p7 | 4:1096500 | CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC | 285498 |
| rs59400847 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056340 | GCTGTCTAACGTACA[C/T]ATGCTGGTGGGCACG | 285498 |
| rs59471070 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096292 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs59750515 | snp | A/T | 0.0053333 | 0.0513634 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1071723 | AATAAAACAGCAAGA[A/T]ACCACTACATACCTA | 285498 |
| rs59790367 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070435 | CTGTGTCAGCGTGGA[C/T]GCCTGGCCTGAGTTA | 285498 |
| rs59830952 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | RNF212 | GRCh38.p7 | 4:1078561 | TGGCTTTTCTGACCC[A/G]TTTCTTTTCCTGGGC | 285498 |
| rs59945268 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070450 | CGCCTGGCCTGAGTT[A/G]CGGGTGGTTTCGTAG | 285498 |
| rs59985183 | snp | G/T | 0.397994 | 0.201489 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1093383 | CATATTGTAACAAAT[G/T]CCAATATTTATGTTA | 285498 |
| rs60035268 | snp | A/G | 0.144841 | 0.226808 | intron-variant, stop-gained, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093699 | ACGGCCTGTGGCTCT[A/G]ATGTCTGTGATAACA | 285498 |
| rs60085185 | snp | C/T | 0.319136 | 0.24025 | synonymous-codon, intron-variant, downstream-variant-500B, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056848 | CTTGCCTAAACACTG[C/T]CTCTGCAGCAGGCTG | 285498 |
| rs60276048 | snp | C/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056375 | CTGGAGGACTGGAAG[C/G]GGGCAGAGCGGGTGG | 285498 |
| rs60315584 | snp | C/T | 0.324855 | 0.23853 | intron-variant | RNF212 | GRCh38.p7 | 4:1057698 | TGTGGTAGAACAGCA[C/T]GCAGTCACCACGTGG | 285498 |
| rs60424574 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1103182 | GAAAAACACAATTTA[C/T]TTAAATTGACTCAAG | 285498 |
| rs60495884 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070397 | TGCCTGGCCTGAGTT[A/G]TGGGTGGTTTTGTAG | 285498 |
| rs60513579 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1075359 | CATGCTTCTGAGGGC[A/C]GTACAGGAAGCATGG | 285498 |
| rs60877270 | in-del | -/ATCACTG | | | intron-variant | RNF212 | GRCh38.p7 | 4:1065538 | GTGGTATGATCACTG[-/ATCACTG]CTCACTGCAGCCTTG | 285498 |
| rs60952893 | in-del | -/GA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1098733 | CCTACGTATAAAACA[-/GA]AGCAGAAACAGCACC | 285498 |
| rs61018678 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1074119 | GCCCACCCTTCACTC[C/T]ATCCAGCAACCACGA | 285498 |
| rs61111892 | in-del | -/CAGGGTCTGCGTGCTCAGTGCTGACGCAGCCTGTGGTAGGGCAGAGGCTG | 0.495855 | 0.045338 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092990 | AAACTACGCCAGGAC[lengthTooLong]GGTGGATGGAACGGA | 285498 |
| rs61295899 | in-del | -/AAAA | 0.349452 | 0.229367 | intron-variant | RNF212 | GRCh38.p7 | 4:1063695 | GTGAGACTCAGTCTC[-/AAAA]AAAAAAAAAAAAAGA | 285498 |
| rs61394227 | in-del | -/CAAAA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1103624 | AACTCACCACATTAA[-/CAAAA]TAAATGAGAATAATT | 285498 |
| rs61401138 | snp | A/G | 0.0106949 | 0.0723399 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072408 | AACCATGGACGTTGG[A/G]TGATAATGATGTATT | 285498 |
| rs61464812 | in-del | -/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070889 | TTTTGTTTTTTTTTT[-/T]AATACTGTTCTTACA | 285498 |
| rs61648964 | in-del | -/AT | 0.397994 | 0.201489 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1093380 | CATATTGTAACAAAT[-/AT]GCCAATATTTATGTT | 285498 |
| rs61735730 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1057240 | GGGGACGGGAGGTGG[C/G]GGCGTGAGAGAACGC | 285498 |
| rs61741410 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, nc-transcript-variant, intron-variant | RNF212, TMED11P, LOC105374344 | GRCh38.p7 | 4:1115390 | TCTTCACTGGTCGTT[C/T]GAAAATTTTCTTCAC | 285498 |
| rs61742501 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1057040 | AACATCATGAATGCT[C/T]GGAGCATCTCTGGTG | 285498 |
| rs61745881 | snp | C/G/T | 3.31539e-05 | 0.00407137 | synonymous-codon, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1081574 | TTACTTACTTGAAAC[C/G/T]GAACTTTTTATTGTG | 285498 |
| rs61746178 | snp | A/C/G/T | 0.000798403 | 0.0199641 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056885 | CTGATGGGCGGCCGG[A/C/G/T]GGGGCAGCCTGGCCT | 285498 |
| rs62294712 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1060287 | CCGAAAGACCCCTGC[C/T]GATCAGCCCGCTGTG | 285498 |
| rs62294713 | snp | G/T | 0.17654 | 0.238964 | intron-variant | RNF212 | GRCh38.p7 | 4:1063477 | GCACTTTGGGAGGCC[G/T]AGGTGGGCAGATCAC | 285498 |
| rs62294714 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | RNF212 | GRCh38.p7 | 4:1064586 | TTCATACGGCCTCTT[G/T]TGTGTGTGTGCAGAG | 285498 |
| rs62294715 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1065688 | ACTCCTAGGCTCAGC[C/T]CCACCTCGGCCTCTC | 285498 |
| rs62294717 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | RNF212 | GRCh38.p7 | 4:1068285 | CATCGACAGGGTCCG[C/G]AAGAAAGCCCTCACT | 285498 |
| rs62294718 | snp | A/C/T | 0.00124019 | 0.0248711 | intron-variant | RNF212 | GRCh38.p7 | 4:1073706 | AAAATTCCAATATTG[A/C/T]GGCTTACGAGATTCG | 285498 |
| rs62294719 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1076375 | TTTGCTTCTCCGAGT[C/T]CACCCAATGAGAGAC | 285498 |
| rs62294746 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | RNF212 | GRCh38.p7 | 4:1082709 | CCCACACAGAAGCTC[C/G]CAGAGGACGGGCACT | 285498 |
| rs62294747 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RNF212 | GRCh38.p7 | 4:1087695 | AAGTCTCATCTCAAA[C/T]TGTAATCCCATGTGT | 285498 |
| rs62294748 | snp | A/G | 0.498908 | 0.0233371 | intron-variant | RNF212 | GRCh38.p7 | 4:1089211 | CTACAGAGCCACAGG[A/G]GTGGAGTTGCCCAAG | 285498 |
| rs62294749 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF212 | GRCh38.p7 | 4:1090358 | CAGACTTGGGGAAGC[A/G]GCCCCAGGTTCCCTT | 285498 |
| rs62294750 | snp | C/G | 0.0456336 | 0.143994 | intron-variant | RNF212 | GRCh38.p7 | 4:1090547 | AGTGTGGCCAGGCAG[C/G]GAGGCCCATGCGGTG | 285498 |
| rs62294752 | snp | C/G | 0.0402882 | 0.136092 | intron-variant | RNF212 | GRCh38.p7 | 4:1095055 | CACAGAAAACACATG[C/G]TCTCAGGATAGCGCA | 285498 |
| rs62294753 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RNF212 | GRCh38.p7 | 4:1097473 | AGCCGGGCGTGGTGA[C/T]GGGCACCTGTAGTCC | 285498 |
| rs62294755 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | RNF212 | GRCh38.p7 | 4:1101587 | GAAATAGTTATGGTC[A/C]ATAGTTATAGAAAAA | 285498 |
| rs62294756 | snp | A/G | 0.348354 | 0.22984 | intron-variant | RNF212 | GRCh38.p7 | 4:1103888 | GTCCCAGCCAATGCT[A/G]TAAAAAAAAGGAAGC | 285498 |
| rs62296477 | snp | C/T | 0.484279 | 0.0872533 | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | RNF212, LOC105374344 | GRCh38.p7 | 4:1113690 | CCAGGTCGTTTGGGC[C/T]GGAGTAGGCGGAGGA | 285498 |
| rs66476034 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1105748 | ATATAAAGCGTCCTT[C/T]CACCGCAGGTCAGGG | 285498 |
| rs66732071 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095938 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs67189766 | snp | A/G | 0.345482 | 0.231048 | intron-variant | RNF212 | GRCh38.p7 | 4:1060114 | AAAAAAAAAAAAAAA[A/G]AAAAAAGAAATTGTT | 285498 |
| rs67353138 | in-del | ACCTCCACGGC/CTGCCCAGGCTGGAGCCAGCCATCTCCACGGT | 0.5 | 0 | intron-variant, frameshift-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093550 | TGGGCAGAGCCTGTG[lengthTooLong]CCATGCCGGAAGCCT | 285498 |
| rs67389082 | in-del | -/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1105749 | ATAAAGCGTCCTTCC[-/T]ACCGCAGGTCAGGGT | 285498 |
| rs67568327 | in-del | ATT/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1093383 | CATATTGTAACAAAT[ATT/G]CCAATATTTATGTTA | 285498 |
| rs71168806 | in-del | -/A | 0.283158 | 0.247791 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058062 | AGTGAGACTCCGGCT[-/A]AAAAAAAAAAAAGCA | 285498 |
| rs71168810 | in-del | -/T/TTT | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1109025 | TTTTTTTTTTTTTTT[-/T/TTT]GAGACAGAGTTTCAC | 285498 |
| rs71299247 | in-del | -/TGATCAC | 0.438386 | 0.164349 | intron-variant | RNF212 | GRCh38.p7 | 4:1065529 | TGGGGTGCAGTGGTA[-/TGATCAC]ATGATCACTGCTCAC | 285498 |
| rs71602717 | in-del | CTGTCTCA/GTGTCTC | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1069204 | CAACAGAGCAAGATT[CTGTCTCA/GTGTCTC]AAAAAAAAAAAGAAA | 285498 |
| rs71602718 | in-del | AAACTACGCCAGGACCAGGGTCTGCGTGCTCAGTGCTGACGCAGCCTGTGGTAGGGCAGAGGCTG/CGACTACGCCAGGAC | 0.5 | 0 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092975 | GTCCACATGAGCTCC[lengthTooLong]GGTGGATGGAACGGA | 285498 |
| rs71602719 | multinucleotide-polymorphism | ACT/CTC | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095215 | ACAGAACCAAGCACA[ACT/CTC]CCCACAGCTCCATGG | 285498 |
| rs71602720 | multinucleotide-polymorphism | AGC/GGG | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095355 | CAGCTCCATGGTCTC[AGC/GGG]ATAGCGCACCTGGCT | 285498 |
| rs71602721 | multinucleotide-polymorphism | AGC/GGG | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095414 | CAGCTCCATGGTCTC[AGC/GGG]ATAGCGCACCTGGCT | 285498 |
| rs71602722 | multinucleotide-polymorphism | ACT/CCC | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095864 | ACAGAACCAAGCACA[ACT/CCC]CCCACAGCTCCATGG | 285498 |
| rs71602724 | multinucleotide-polymorphism | AGCATAGC/GGGATAGT | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095768 | CAGCTCCATGGTCTC[AGCATAGC/GGGATAGT]GCACCTGGCTCATCA | 285498 |
| rs71602725 | multinucleotide-polymorphism | ACT/CCC | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095805 | ACAGAACCAAGCACA[ACT/CCC]CCCACAGCTCCATGG | 285498 |
| rs71604346 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1057233 | GGCCAGCGGGGACGG[A/G]AGGTGGGGGCGTGAG | 285498 |
| rs71604347 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079219 | AACATAGAGTCAACA[C/T]AGGACCAACATGGGA | 285498 |
| rs71604349 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095716 | ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs71604351 | snp | C/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095859 | TCATCACAGAACCAA[C/G]CACACCCCCCACAGC | 285498 |
| rs71604352 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1096028 | CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC | 285498 |
| rs71604353 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095497 | CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC | 285498 |
| rs71604354 | snp | C/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095505 | TCATCACGGAACCAA[C/G]CACACCCCCCACAGC | 285498 |
| rs71604355 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095532 | CAGCTCCATGGTCTC[A/G]GGATAGCGCACCTGG | 285498 |
| rs71604356 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095792 | CACCTGGCTCATCAC[A/G]GAACCAAGCACACCC | 285498 |
| rs71604357 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095866 | AGAACCAAGCACACC[C/T]CCCACAGCTCCATGG | 285498 |
| rs71604358 | snp | A/C | 0.431621 | 0.171796 | intron-variant | RNF212 | GRCh38.p7 | 4:1105326 | TGGCGGCCCAGCCAC[A/C]CACCACATCCCCAGG | 285498 |
| rs71634674 | multinucleotide-polymorphism | CA/GG | 0 | 0 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058015 | GCGGTGAGCCAAGAT[CA/GG]TGCTACTGCACTCCA | 285498 |
| rs71640378 | in-del | -/AACAA | 0.495708 | 0.0461266 | intron-variant | RNF212 | GRCh38.p7 | 4:1103622 | GCAACTCACCACATT[-/AACAA]AATAAATGAGAATAA | 285498 |
| rs71640379 | in-del | -/T/TT/TTT | 0.489722 | 0.0709447 | intron-variant | RNF212 | GRCh38.p7 | 4:1109010 | TGGCCATAATTAGCC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 285498 |
| rs72479341 | snp | A/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067713 | CTACTAAAGTACAAA[A/T]ATTAGCCAGGTGAGG | 285498 |
| rs73061793 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | RNF212 | GRCh38.p7 | 4:1100111 | TTCCTTGCTAGAGTC[C/T]CGGCTGTCAACACTA | 285498 |
| rs73061799 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1102458 | TCTCTATGTATACAT[A/G]GACACACACAGTTAA | 285498 |
| rs73063716 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1106564 | GAAATCAGAGAAAAG[C/T]GGTACTCAAAATGAT | 285498 |
| rs73063723 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | RNF212 | GRCh38.p7 | 4:1108577 | TTGGAAGGATTTATA[C/G]AACTAACATTCTTTT | 285498 |
| rs73063735 | snp | C/G | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111985 | GAGGCCAAGGCCGGT[C/G]ATTGTTAGAGGACAG | 285498 |
| rs73072277 | snp | C/T | 0.0930568 | 0.194599 | intron-variant | RNF212 | GRCh38.p7 | 4:1067308 | CTAAAAATCCTGTCA[C/T]ATATAAAACAAAAAA | 285498 |
| rs73074159 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | RNF212 | GRCh38.p7 | 4:1089671 | GAATTGCAGTCCCCA[C/T]GTGTCAAGGGAGGGA | 285498 |
| rs73074161 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | RNF212 | GRCh38.p7 | 4:1090110 | AGGGTGACAGGATGG[A/G]GTTGGGGTGACAGGA | 285498 |
| rs73074169 | snp | C/T | 0.29175 | 0.246489 | intron-variant | RNF212 | GRCh38.p7 | 4:1091377 | TTCTGAGAGTACCAA[C/T]ATAAGGAGGAAAGAG | 285498 |
| rs73188348 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF212 | GRCh38.p7 | 4:1100957 | TCAGATGGAATTCTG[C/T]GGCTGAAATCACCTG | 285498 |
| rs73792252 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1068515 | CTTTGTGCTTATTAT[C/T]CTCTATGTTACATCT | 285498 |
| rs73792255 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073387 | AAGGAGCCAGTTATC[G/T]CCTGTGACTTGTTAC | 285498 |
| rs73792258 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RNF212 | GRCh38.p7 | 4:1081069 | ATTCCATATAAGGCA[A/C]ACCAGGTCAGCCCCT | 285498 |
| rs73792259 | snp | A/G | 0.00262222 | 0.0361142 | intron-variant | RNF212 | GRCh38.p7 | 4:1081374 | GGCAGGTGCAGAATC[A/G]GAAAGACCTGCAGGT | 285498 |
| rs73792260 | snp | C/G | 0.0452528 | 0.143452 | intron-variant | RNF212 | GRCh38.p7 | 4:1082672 | CGGCCCGACATACAA[C/G]TTCACTTTCTGCCTC | 285498 |
| rs73792261 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1083219 | GAGGATATCAGGTAA[A/G]GAAAATAAAAAGGCT | 285498 |
| rs73792264 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1091431 | AGAAAAGAGCTATTT[C/T]GTATGAGTTGAGTGT | 285498 |
| rs73792265 | snp | C/G | 0.0138723 | 0.0821202 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093581 | GAGAGGCACGAGAGG[C/G]AGAGCAGACAGGTGG | 285498 |
| rs73792266 | snp | C/T | 0.00185443 | 0.0303937 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093878 | CCTGGTCTGGGTGCC[C/T]GTGTTGTGCTGACCC | 285498 |
| rs73792268 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1094141 | GCAGGGGTCCATCCT[C/T]AGTCTCCTGCCTCAG | 285498 |
| rs73792270 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | RNF212 | GRCh38.p7 | 4:1098542 | GACCTGGCTCTGGCT[C/T]GGATGGGGTAGGAGC | 285498 |
| rs73792272 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1101049 | CAGATGCCAAAGACT[A/T]GATTTTGATCTGCAA | 285498 |
| rs73792273 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF212 | GRCh38.p7 | 4:1101178 | CGACCCCTAGACCCA[C/T]GGGCCTAACGACTGG | 285498 |
| rs73793929 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1059743 | CACACAGAACCACAA[A/G]TAATAACGATGGCAG | 285498 |
| rs73793931 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF212 | GRCh38.p7 | 4:1065030 | ACACACATTGTGCCT[A/G]TCCATTCATCTGATG | 285498 |
| rs73793932 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1065277 | CTTCCAATTCCTCCG[C/T]GTCCTTAACAACACT | 285498 |
| rs74331143 | snp | G/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1089004 | CCTCTGCTAGGGCAG[G/T]GCAGAAGGGAAATGT | 285498 |
| rs74384021 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | RNF212 | GRCh38.p7 | 4:1065278 | TTCCAATTCCTCCGC[A/G]TCCTTAACAACACTT | 285498 |
| rs74397095 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1110273 | GCATAGGAAAAAATG[A/C]AAACAGCCAATAAAC | 285498 |
| rs74490855 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1109750 | TGACCCACCACAGAA[A/C]AACCCACTTCACGCT | 285498 |
| rs74506216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056790 | GAGCTTCTTTACACA[C/T]GCACTTTCCCAAGAG | 285498 |
| rs74578663 | snp | C/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095156 | ACAGAACCAAGCACG[C/G]CCCCCACAGCTCCAT | 285498 |
| rs74629913 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1082721 | CTCCCAGAGGACGGG[C/T]ACTGGGCGTGTTTGG | 285498 |
| rs74701499 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1110255 | ATGAGGAGACCTGAA[C/T]AGGCATAGGAAAAAA | 285498 |
| rs74781535 | snp | G/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1091145 | AATGGCTACTGGTTT[G/T]AGGAATGGCCTCCTG | 285498 |
| rs74783365 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF212 | GRCh38.p7 | 4:1090350 | CTGGCTTCCAGACTT[A/G]GGGAAGCGGCCCCAG | 285498 |
| rs74783744 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1069222 | TCTCAAAAAAAAAAA[A/G]AAATCTATGAATCCA | 285498 |
| rs74789044 | snp | C/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1067751 | CGCACGCCTGTAATC[C/G]CAGCTACTCAGGAGG | 285498 |
| rs74811778 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1063300 | CACTTCATAATTTCA[A/G]AAGTTACTATAAAGC | 285498 |
| rs74880304 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF212 | GRCh38.p7 | 4:1110159 | AGGAAATCACGTGCG[A/G]CCAAAAGACAAAGGG | 285498 |
| rs75000940 | snp | A/T | | | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072289 | CGCACAGAGGATTTT[A/T]AGGGTGTGGCACTAT | 285498 |
| rs75149107 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1079496 | CACAGCCCACCCCTC[A/T]CACCCACGGGACCAG | 285498 |
| rs75150296 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1082090 | TACTGTACTACTGCA[C/G]TCCTGCTTGGGTGAC | 285498 |
| rs75170483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1069714 | CCCACCAATAGAGGA[C/T]GGTCTGGTCTCCGGA | 285498 |
| rs75180289 | snp | A/G | 0.375 | 0.216506 | intron-variant | RNF212 | GRCh38.p7 | 4:1095379 | CACCTGGCTCATCAC[A/G]GAACCAAGCACAACT | 285498 |
| rs75239517 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1074796 | AGCTTTTGTCTCTGT[A/C]CCTTCAGCCTCTGCC | 285498 |
| rs75250153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1104252 | CTCCAAAATTTATGC[A/G]GACATGCGAAGATGA | 285498 |
| rs75252437 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1076917 | GACTGTCTGGTCTGC[A/G]AAGTCCAAATGTTTT | 285498 |
| rs75281182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1098610 | AGGCACAAGCAGTAT[A/G]TCCAACACCACAGGC | 285498 |
| rs75316958 | snp | A/C | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1082905 | CTCCTGATTCCAGAC[A/C]ACTCTAAAATGCACT | 285498 |
| rs75320593 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1076841 | GTCATGGTCATGCCT[A/G]TTAGCTTCCATACTT | 285498 |
| rs75398934 | snp | A/T | 0.0298908 | 0.118541 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073451 | AAAAGCTGCACCATT[A/T]TGGTGAATATGTAGC | 285498 |
| rs75436204 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1107967 | GGCATTGTTTTAAGC[C/T]TGCAGCAGTAATTGA | 285498 |
| rs75477718 | snp | A/G | 0.000363907 | 0.0134841 | intron-variant | RNF212 | GRCh38.p7 | 4:1079602 | TGGGAAATGCCACAC[A/G]TCTGGTATACAGAGG | 285498 |
| rs75494992 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1102448 | ACTGGAAAAATCTCT[A/G]TGTATACATGGACAC | 285498 |
| rs75675349 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF212 | GRCh38.p7 | 4:1066331 | TCATTTGCTGCCCTC[C/T]GCTTTTCTTTTTTCT | 285498 |
| rs75724850 | snp | C/T | 0.031825 | 0.122064 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072125 | GAAGAGATGGGGGAA[C/T]CATAAGTGTGTATTG | 285498 |
| rs75745573 | snp | C/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083679 | AGCCAGTGAACCCCA[C/G]TGAGTTTGTTTGTTT | 285498 |
| rs75811516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1090126 | GTTGGGGTGACAGGA[C/T]AGGGATGGGGTACCA | 285498 |
| rs75844542 | snp | A/C | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1063869 | GCAGAGACCCAGTCT[A/C]AAAAAAAAAAAAATG | 285498 |
| rs75865688 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1060993 | AAGTGCGAAACTGGA[A/C]AAAATGGTAGAAACA | 285498 |
| rs75881267 | snp | C/G | 0.0410537 | 0.137264 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112544 | TTGACACCAGGGCCC[C/G]GCGCTGCCCATGGAA | 285498 |
| rs75885405 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083814 | AGGTTGTGGCTGGGG[A/G]TGCAGAGGGTACTAC | 285498 |
| rs75938345 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF212 | GRCh38.p7 | 4:1090323 | ACAGACAGGAGGCAG[A/C]AGGGTCACAAGCTGG | 285498 |
| rs76009948 | snp | A/C | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1102991 | ACTAAAAAAATACAA[A/C]AAAAAAAAAAATCAC | 285498 |
| rs76018863 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1067698 | TTTTGTATTTTTAGT[A/G]GAGACGGGGTTTCCC | 285498 |
| rs76056108 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | RNF212 | GRCh38.p7 | 4:1106009 | ATGCATGGGGGACTT[A/T]GGCGCTTACTCCTGG | 285498 |
| rs76082306 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096115 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs76115034 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF212 | GRCh38.p7 | 4:1085167 | TATTCAACGCGTCTC[A/G]TAGAATCTAAGGCAT | 285498 |
| rs76172097 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | RNF212 | GRCh38.p7 | 4:1061313 | AGGGGGTGGGCTCAA[C/G]GTGGGAGGGGAACGC | 285498 |
| rs76192970 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | RNF212 | GRCh38.p7 | 4:1061443 | GGGAAATGCTGAGAA[A/C]AAGAGAGCCAGACAG | 285498 |
| rs76213161 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1082639 | ACCCAGAGTCACTTA[C/T]CCTGACAGCCTGTGT | 285498 |
| rs76276522 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1067644 | CTGAGGTGGATGGAT[C/G]GCTTGAGGCCAGGGG | 285498 |
| rs76277570 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | RNF212 | GRCh38.p7 | 4:1074660 | CCCTGCTTGGCATGG[C/T]CCTCTGAGCTGCCTG | 285498 |
| rs76319257 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | RNF212 | GRCh38.p7 | 4:1059207 | AAGGCAGCCTCCGTG[C/T]CCCCGACAGGGGTCT | 285498 |
| rs76327831 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1067685 | TAGAGACAGGGTGTC[A/G]CCATGTTGACGAGGC | 285498 |
| rs76337818 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNF212 | GRCh38.p7 | 4:1062417 | GAACAAAACCCAATA[A/G]TCATCTCAAAAGAGA | 285498 |
| rs76356548 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1109752 | ACCCACCACAGAACA[A/C]CCCACTTCACGCTAC | 285498 |
| rs76360801 | snp | A/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067890 | AAAAAAAAAAAGAAA[A/T]ACCTAAAGTGTAAGT | 285498 |
| rs76423765 | in-del | -/CCAGGGTCTGCGTGCTCAGTGCTGACGCAGCCTGTGGTAGGGCAGAGGCTG | | | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092989 | CAAACTACGCCAGGA[lengthTooLong]GGTGGATGGAACGGA | 285498 |
| rs76432402 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1066866 | CATATCCAGGAAATC[A/C]CTGCCACATCCAACA | 285498 |
| rs76554135 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1081893 | TCAGCACATGGCCAC[C/T]GCGGGTGTTAAAGGT | 285498 |
| rs76622058 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF212 | GRCh38.p7 | 4:1068590 | ATGTTATGTTTTGTA[A/G]GGTAATGAGAAGATA | 285498 |
| rs76667607 | snp | C/G/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1088998 | GGAGAACCTCTGCTA[C/G/T]GGCAGTGCAGAAGGG | 285498 |
| rs76700648 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070419 | GTTTTGTAGGACTGT[A/G]CTGTGTCAGCGTGGA | 285498 |
| rs76876257 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1069109 | CCAGCTACTTGGGAG[A/G]CTGAGGCACAAGAAT | 285498 |
| rs76934875 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072290 | GCACAGAGGATTTTT[A/G]GGGTGTGGCACTATT | 285498 |
| rs76992730 | in-del | -/AAAC | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083640 | GAGACTCTGTCTCAA[-/AAAC]AAACAAACAAACAAA | 285498 |
| rs77018707 | snp | C/T | 0.0183706 | 0.094063 | intron-variant, utr-variant-5-prime | RNF212 | GRCh38.p7 | 4:1099766 | TCATGGCAGAGGGCG[C/T]AAGGAATGGAGGAAA | 285498 |
| rs77029034 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | RNF212 | GRCh38.p7 | 4:1089558 | ACTGCTGGGAAGGTA[C/T]GATTGTGTTTTGAAA | 285498 |
| rs77036576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1067686 | CCTCGTCAACATGGT[A/G]ACACCCTGTCTCTAC | 285498 |
| rs77048510 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1059704 | CCTCACACCAGTGAT[C/T]AAAACAAAACCCTGT | 285498 |
| rs77077625 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF212 | GRCh38.p7 | 4:1080047 | CTGCTGGACTAGGAC[A/G]TTCTGAGAGTGGGAT | 285498 |
| rs77129670 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | RNF212 | GRCh38.p7 | 4:1081312 | AGTCAACTGTATGGA[A/T]TAGCAAAATCTGGGG | 285498 |
| rs77131413 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083934 | AATGAAAGTAATTCC[A/C]CATTTTGTGCATTTT | 285498 |
| rs77260074 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF212 | GRCh38.p7 | 4:1109900 | GTGGGGTGAGGGGGT[C/T]CCCTTCTAACAGCCT | 285498 |
| rs77269282 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | RNF212 | GRCh38.p7 | 4:1067209 | CAACATATGAATTTT[G/T]GGGGGACTCAAATCA | 285498 |
| rs77401800 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | RNF212 | GRCh38.p7 | 4:1061791 | AGGTAAAATACCCAA[A/G]CAAACAAAAACCAAT | 285498 |
| rs77408406 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1065508 | GGTCTCACTCTGTCA[A/G]CCAGTCTGGGGTGCA | 285498 |
| rs77448219 | snp | G/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1059169 | GGGGGTTGCCGGCTT[G/T]TGGGGCAGGAGGCCC | 285498 |
| rs77511517 | snp | A/G | 0.116488 | 0.211364 | intron-variant | RNF212 | GRCh38.p7 | 4:1068557 | CTCCAACAATACAGT[A/G]TTATCATTGTTGCTT | 285498 |
| rs77521705 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1069727 | GATGGTCTGGTCTCC[A/G]GAGGAAATACCAGAC | 285498 |
| rs77642982 | snp | A/T | | | utr-variant-3-prime, intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1072701 | AAAAATATTGTCTCT[A/T]AAATTCAAAGGTCAA | 285498 |
| rs77685524 | snp | A/C | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1063696 | TGAGACTCAGTCTCA[A/C]AAAAAAAAAAAAAAA | 285498 |
| rs77794150 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1099044 | ATGAGCCTAGAGCCA[A/G]AACAGCCAAGAAGTC | 285498 |
| rs77835163 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1067573 | CCGTAAAAAATAATG[A/G]AATACCTAGGGCCGG | 285498 |
| rs77843211 | snp | C/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1067766 | CCAGTTACTCAGAAG[C/G]CTGAAGCATGAGAAT | 285498 |
| rs77924371 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | RNF212 | GRCh38.p7 | 4:1058442 | CATGTTAACACATCA[C/T]GGTGCTTTGAGGACG | 285498 |
| rs77969740 | snp | G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1066089 | AGATACTATCTTGCT[G/T]TTTTTTTTTTTTCTC | 285498 |
| rs78003862 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1081942 | AACAGGAGCCACTAA[C/T]GCACCAGCTTTGAAA | 285498 |
| rs78029756 | snp | C/G | 0.00111441 | 0.0235789 | intron-variant, utr-variant-5-prime | RNF212 | GRCh38.p7 | 4:1099859 | CCTGTGCGGGATCCA[C/G]GGGGCTCTCCTCACG | 285498 |
| rs78045754 | snp | C/T | 0.101301 | 0.200969 | intron-variant | RNF212 | GRCh38.p7 | 4:1095083 | GCACCTGGCTCATCA[C/T]GGAACCAAGCACACT | 285498 |
| rs78092679 | snp | G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1066090 | GATACTATCTTGCTG[G/T]TTTTTTTTTTTCTCT | 285498 |
| rs78238785 | snp | A/G | 0.0933755 | 0.194856 | intron-variant | RNF212 | GRCh38.p7 | 4:1108407 | TCATTCTTTTTACCT[A/G]TAAAATAAAAATAGG | 285498 |
| rs78248026 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1106661 | AGTAAATGACCTGAA[C/T]ATTCCACTCAAGCTA | 285498 |
| rs78300451 | snp | A/C | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1102603 | AAAAAACAAAAAAAA[A/C]ACACTTTGGGAGGCT | 285498 |
| rs78372091 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RNF212 | GRCh38.p7 | 4:1081896 | GCACATGGCCACTGC[A/G]GGTGTTAAAGGTGTG | 285498 |
| rs78388282 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF212 | GRCh38.p7 | 4:1075474 | GCAAGAGACTGGGGG[A/G]TGGTGCCATGTACTT | 285498 |
| rs78457483 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095473 | CAGCTCCACGGTCTC[A/G]GGATAGCGCACCTGG | 285498 |
| rs78461909 | snp | C/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096036 | TCATCACGGAACCAA[C/G]CACACCCCCCACAGC | 285498 |
| rs78497787 | snp | C/T | 0.0766824 | 0.180169 | intron-variant | RNF212 | GRCh38.p7 | 4:1066838 | TTTTTTTTTGTTGCC[C/T]GTGCTTTGGTATCAT | 285498 |
| rs78498193 | snp | A/T | | | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1071625 | ATGGGCCAAATACCT[A/T]AACAGACACTTCAGC | 285498 |
| rs78510634 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1082629 | CAACATCCTCACCCA[C/G]AGTCACTTATCCTGA | 285498 |
| rs78569536 | snp | G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1066831 | TTTAATTTTTTTTTT[G/T]GTTGCCTGTGCTTTG | 285498 |
| rs78572547 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1065243 | ACACCATTTCACATT[C/G]TCACCAACAGTGCAC | 285498 |
| rs78585429 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1106394 | CCTGATAATTAAAAA[A/C]CCCACATAGCCATAT | 285498 |
| rs78597275 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF212 | GRCh38.p7 | 4:1099189 | GATAAGCCAGGTGCC[A/G]GAATTTTCAAAGTGC | 285498 |
| rs78619937 | snp | G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1066832 | TTAATTTTTTTTTTT[G/T]TTGCCTGTGCTTTGG | 285498 |
| rs78622782 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | RNF212 | GRCh38.p7 | 4:1060502 | GAGCTCCTCAGGGTG[C/T]CAAGGGGGCGCCATG | 285498 |
| rs78629599 | snp | A/C | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1078057 | TTCTGACTCCGGGTC[A/C]CTCCATCATCCGGCT | 285498 |
| rs78890071 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1056323 | AAAGTACAGTCGCAC[G/T]GGCTGTCTAACGTAC | 285498 |
| rs78930395 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF212 | GRCh38.p7 | 4:1079743 | ACTTACCTCTAACAA[C/T]GTCAGTTGAAATACA | 285498 |
| rs78958397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1074351 | GGCATCTCCTGTTCC[C/T]AGGCTCCTTGCCTCA | 285498 |
| rs78978823 | snp | C/T | 0.0112596 | 0.0741822 | missense, upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113457 | TTACAGAACACCCAG[C/T]TGGCCATGCCAGGCG | 285498 |
| rs79053889 | snp | A/G | 0.261884 | 0.249717 | intron-variant | RNF212 | GRCh38.p7 | 4:1089519 | CTTCTGAGTTTATGC[A/G]GGAATGAGTTAAAAC | 285498 |
| rs79059075 | snp | A/C | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1060099 | AGCGAAACTCCATCA[A/C]AAAAAAAAAAAAAAG | 285498 |
| rs79067760 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1058883 | GGAGCACGAGCTTCC[C/T]CCCCCGCCTCTCCCA | 285498 |
| rs79149095 | snp | A/G | 0.308414 | 0.24308 | intron-variant | RNF212 | GRCh38.p7 | 4:1095438 | CACCTGGCTCATCAC[A/G]GAACCAAGCACAACT | 285498 |
| rs79226746 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF212 | GRCh38.p7 | 4:1086370 | CCAGACCCCAAGAGA[C/G]TGACTAGAGTCTAGG | 285498 |
| rs79249955 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1061264 | CACAGCTGCACCAGG[G/T]TGGGTAGCTGAGGAC | 285498 |
| rs79277426 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1088039 | TAGAGTGGGGCACTG[C/T]TATAAATGTAACTAA | 285498 |
| rs79329953 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | RNF212 | GRCh38.p7 | 4:1087631 | GAATGGGGTTGAGAG[A/G]TGACAGAATGTGGTG | 285498 |
| rs79366377 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058073 | GGCTAAAAAAAAAAA[A/G]AGCAAACTCTAAAGT | 285498 |
| rs79373704 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF212 | GRCh38.p7 | 4:1069513 | GCCTGTGTGGTCAGG[C/T]GACCAAGGTGAACAT | 285498 |
| rs79401639 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067886 | AAAAAAAAAAAAAAA[A/G]AAATACCTAAAGTGT | 285498 |
| rs79404168 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1088273 | GGAGCAAAGGTCACT[C/T]TTGCTGTGCTTTAGC | 285498 |
| rs79435154 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | RNF212 | GRCh38.p7 | 4:1074989 | CGTCCCTTCGAACTA[C/T]ATTCCATTTGCTGCT | 285498 |
| rs79521655 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1074916 | TCATTTCTGGATCCT[C/T]CCATCCGCTAGGATG | 285498 |
| rs79560074 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1083001 | CCACCACAGTGAGGC[C/T]GGGCAAGACGGGGTC | 285498 |
| rs79620907 | snp | C/T | 0.375 | 0.216506 | intron-variant | RNF212 | GRCh38.p7 | 4:1079010 | AACATAGGACCAACA[C/T]AGGGTCAACACAGGA | 285498 |
| rs79621814 | snp | C/T | 0.469642 | 0.119404 | intron-variant | RNF212 | GRCh38.p7 | 4:1095480 | ACGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs79787903 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1065269 | TGCACATGCTTCCAA[C/T]TCCTCCGCGTCCTTA | 285498 |
| rs79830754 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1107544 | CAGGCTCCGCCTCCC[A/G]GGTTCACGCATTCTC | 285498 |
| rs79913309 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067773 | TCAGGCAATTCTCCT[A/G]CCTCAGCTTTCCTAG | 285498 |
| rs79971155 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF212 | GRCh38.p7 | 4:1100043 | CTTGAAACACACAGA[C/T]TGTACTGGCTACAGC | 285498 |
| rs79998857 | snp | C/T | 0.031825 | 0.122064 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1071698 | GTCATATGTTATCAA[C/T]GAAATGCAAAATAAA | 285498 |
| rs80031357 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF212 | GRCh38.p7 | 4:1102476 | CACACACAGTTAAAA[C/T]CTGTGTTGTTCAAGA | 285498 |
| rs80130161 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1069033 | GGCAACATGGCGAAA[C/G/T]TCCATCTCTACTAAA | 285498 |
| rs80144051 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1067729 | ATTAGCCAGGTGCAG[C/T]GGTGCACGCCTGTAA | 285498 |
| rs80179646 | snp | G/T | | | intron-variant, utr-variant-5-prime | RNF212 | GRCh38.p7 | 4:1099832 | CCGACGGCGCAAGCG[G/T]ACACGGGTACCCCTG | 285498 |
| rs80257060 | snp | G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1074692 | AGGCCAGCTTTCTCA[G/T]GGAGCTGTCCACTAA | 285498 |
| rs111155337 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1113106 | GCCGTTTCTCCCCCT[C/T]GGCCCCCCACGCGCC | 285498 |
| rs111216168 | snp | C/G | 0.44768 | 0.153045 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112987 | GTCCCCCTCTCCCCA[C/G]GGGCCCCTCATCACG | 285498 |
| rs111216208 | snp | C/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087010 | GTGAGAAGATGGGGT[C/G]GGGGAGAGAGGATGG | 285498 |
| rs111216249 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087136 | GTGGGGGAGAGAGGA[C/T]GGGGTGGGGGTGAGA | 285498 |
| rs111216444 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087165 | GAGGATGGGTGGGGG[A/G]GAGAGGATGGCATTG | 285498 |
| rs111233579 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1081910 | CGGGTGTTAAAGGTG[C/T]GAAATTAAGACCTGA | 285498 |
| rs111234626 | in-del | -/A | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1083117 | TATGTAGAGAGTGGG[-/A]TTGGCCTGTGCAACC | 285498 |
| rs111240158 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079043 | AACATGGGACCAACA[C/T]AGAGTCAACACAGGA | 285498 |
| rs111241058 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095925 | AGAACCAAGCACACC[C/T]CCCACAGCTCCATGG | 285498 |
| rs111266324 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096064 | AGCTCCACGGTCTCG[A/G]GATAGCGCACCTGGC | 285498 |
| rs111322195 | snp | A/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1073940 | AAGGGCTCTACTAGG[A/T]ATTTTAGGTGAAAAA | 285498 |
| rs111373612 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079252 | AACACAGGGTCAACA[C/T]AGGACCAACATGGGA | 285498 |
| rs111384741 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079120 | AACACAGGGTCAACA[C/T]AGGACCAACATAGGA | 285498 |
| rs111419884 | snp | C/G/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1078999 | AACACAGGACCAACA[C/G/T]AGGACCAACACAGGG | 285498 |
| rs111436949 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087582 | GTGTGACAGGAGCAG[A/G]GAGTGGGTAATAGGA | 285498 |
| rs111481773 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1074067 | ACAGGTTGGAGCTAA[C/T]GCTGCTCAGAGCTGT | 285498 |
| rs111484186 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095868 | AACCAACCACACCCC[C/T]CACAGCTCCATGGTC | 285498 |
| rs111491041 | snp | A/C/T | 0.0198134 | 0.0978804 | intron-variant | RNF212 | GRCh38.p7 | 4:1105314 | AGTCTCCCTTCCTGG[A/C/T]GGCCCAGCCACCCAC | 285498 |
| rs111509271 | snp | A/G | 0.5 | 0 | downstream-variant-500B, intron-variant | RNF212 | GRCh38.p7 | 4:1071212 | GGTTTTTTAAATACT[A/G]TTCTTACAATTTTTT | 285498 |
| rs111533894 | snp | A/G | 0.267908 | 0.249358 | intron-variant | RNF212 | GRCh38.p7 | 4:1077177 | AGGTTGCAGTGAGCC[A/G]AGATCTCGCCACTGC | 285498 |
| rs111537736 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1101199 | TAACGACTGGCACTC[A/G]CAGTGCAGTAGCCGT | 285498 |
| rs111543294 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF212 | GRCh38.p7 | 4:1078852 | GACCAACACAGGACC[A/G]ACATAGGACCAACAC | 285498 |
| rs111563147 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1078989 | ACACAGGGTCAACAC[A/G]GGACCAACATAGGAC | 285498 |
| rs111572776 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1058974 | TTCAGTGCCCCACCC[A/G]TGTTTGCTTTCTCCA | 285498 |
| rs111609415 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096279 | GGAACCAAGCACACC[C/T]CCCACAGCTCCACGG | 285498 |
| rs111625655 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1082089 | CTACTGTACTACTGC[A/G]CTCCTGCTTGGGTGA | 285498 |
| rs111628797 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096340 | AACCAACCACACCCC[C/T]CACAGCTCCACGGTC | 285498 |
| rs111661076 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1098974 | TTCCATGGCCTTCTG[C/G]GTGAGGGGGACTGAG | 285498 |
| rs111702053 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1078846 | ACACGGGACCAACAC[A/G]GGACCAACATAGGAC | 285498 |
| rs111722177 | snp | C/G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114071 | ATGTGGGAGTTGGGG[C/G/T]GGGTGTGGGGGCGTG | 285498 |
| rs111747006 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | RNF212 | GRCh38.p7 | 4:1083629 | GGTGACAGAGTGAGA[C/T]TCTGTCTCAAAAACA | 285498 |
| rs111757425 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF212 | GRCh38.p7 | 4:1094530 | AAAAGCTGCCAGGGG[A/G]GGGGACCATGGAGCC | 285498 |
| rs111893367 | snp | A/G | 1.72347e-05 | 0.00293548 | intron-variant | RNF212 | GRCh38.p7 | 4:1073714 | AATATTGCGGCTTAC[A/G]AGATTCGGACTCCCA | 285498 |
| rs111916592 | in-del | -/T | 0.102014 | 0.201495 | intron-variant | RNF212 | GRCh38.p7 | 4:1080687 | GGCCCACGAGACCCC[-/T]CTCTGCCTGAGCCTT | 285498 |
| rs112014944 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | RNF212 | GRCh38.p7 | 4:1103624 | AACTCACCACATTAA[C/T]AAAATAAATGAGAAT | 285498 |
| rs112078081 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1084020 | ATGGCATGATCTTGG[C/T]TCACCGCAACCTCTG | 285498 |
| rs112095307 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1104778 | CCCGATTTGGCCTGC[A/C]ATCTATGAGCTAGAA | 285498 |
| rs112107564 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096493 | GATAGCGCACCTGGC[C/T]CATCACGGAACCAAG | 285498 |
| rs112116120 | snp | A/C/T | 0.00716266 | 0.059414 | intron-variant, missense | RNF212 | GRCh38.p7 | 4:1094232 | GAGCTGCACTCTTCA[A/C/T]GGAAGAGGGAAAGGA | 285498 |
| rs112182981 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1080134 | GCTCGGTACGCACTA[G/T]TTCCTTCATTTGCCA | 285498 |
| rs112213665 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1062196 | AAAGAAGTGTGCTGA[C/T]CAGTATCTCTTATGA | 285498 |
| rs112262072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1108521 | GTATCACTTACAGGT[G/T]TTCATGTTCTGACAG | 285498 |
| rs112262402 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1069972 | GGACGCCTAGCCTGA[A/G]TTACGGGTGGTTTTG | 285498 |
| rs112264228 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079088 | ACACAGGGTCAACAC[A/G]GGACCAACATAGGAC | 285498 |
| rs112278468 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1076259 | CAGCAGCCTGAGGTC[C/T]CCAGGCCTGGAGCAG | 285498 |
| rs112353217 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF212 | GRCh38.p7 | 4:1097327 | AGCGTCTCGTAGGTC[A/G]GGAGCGGTGGCTCAA | 285498 |
| rs112390261 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095809 | AACCAAGCACACCCC[C/T]CACAGCTCCATGGTC | 285498 |
| rs112406116 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | RNF212 | GRCh38.p7 | 4:1069514 | CCTGTGTGGTCAGGC[G/T]ACCAAGGTGAACATC | 285498 |
| rs112424657 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079099 | ACACAGGACCAACAT[A/G]GGACCAACACAGGGT | 285498 |
| rs112521862 | snp | A/G | 0.5 | 0 | synonymous-codon, stop-lost, intron-variant, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073018 | TATTGGAAGTGTTTT[A/G]GAGTTGGTGAGTTCC | 285498 |
| rs112532891 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1060908 | TTCAACAACTCATTC[A/G]ATGAGTGCTTGTTGA | 285498 |
| rs112533783 | in-del | -/TC | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079494 | GCCACAGCCCACCCC[-/TC]TCACCCACGGGACCA | 285498 |
| rs112573123 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095945 | CAGCTCCATGGTCTC[A/G]GGATAGCGCACCTGG | 285498 |
| rs112575714 | snp | C/T | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096233 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs112586714 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096396 | CGGAACCAAGCACAC[C/T]CCCCACAGCTCCACG | 285498 |
| rs112611497 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112772 | CTCCCCCACGCCCTC[C/T]TCCCCTGGCGTCTCC | 285498 |
| rs112630923 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079046 | ATGGGACCAACATAG[A/G]GTCAACACAGGACCA | 285498 |
| rs112654968 | in-del | -/C | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1110809 | CACCCCTTTTCACCA[-/C]TTTTTTGTGTGTCTT | 285498 |
| rs112655611 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1070381 | GCTGTGTCAGCGTGG[A/G]TGCCTGGCCTGAGTT | 285498 |
| rs112697221 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1070630 | GGTTTTGTAGGACTG[C/T]GCTGTGTCAGCGTGG | 285498 |
| rs112698965 | snp | C/T | 4.97146e-05 | 0.00498546 | intron-variant | RNF212 | GRCh38.p7 | 4:1079723 | AGGCTTTGAGTGAGC[C/T]CAGGACTTACCTCTA | 285498 |
| rs112740909 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095362 | ATGGTCTCAGCATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs112742902 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096011 | ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs112758484 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1104153 | AGAGATACTAACACT[A/G]TTGCACAAAGCCTCC | 285498 |
| rs112759663 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1090674 | ACAGAGAAACAGATA[C/T]TGCATCTAGCAGCCA | 285498 |
| rs112830653 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1083523 | TGGGGCTGTAATCCC[A/C]GCTACTCAGGAGGCT | 285498 |
| rs112857408 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1085983 | CACAACCTCTTGTTA[C/T]CAGACAGGCTATGCT | 285498 |
| rs112883152 | snp | C/T | 0.132751 | 0.2208 | intron-variant | RNF212 | GRCh38.p7 | 4:1087967 | TATAAATCACCCAGT[C/T]TCAGGTAGTTCTTTA | 285498 |
| rs113014651 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1095474 | AGCTCCACGGTCTCG[A/G]GATAGCGCACCTGGC | 285498 |
| rs113015962 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1080058 | GGACGTTCTGAGAGT[A/G]GGATCCCGAATTGAC | 285498 |
| rs113017127 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096323 | CACCTGGCTCATCAC[A/G]GAACCAACCACACCC | 285498 |
| rs113027782 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096425 | CGGTCTCGGGATAGC[A/G]CACCTGGCTCATCAC | 285498 |
| rs113028087 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1078922 | AACACAGGACCAACA[C/T]GGGACCAACACAGGG | 285498 |
| rs113029661 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1066969 | GAATTGACTTTTCTA[C/T]ATAGTGTTAGGAAGG | 285498 |
| rs113061374 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF212 | GRCh38.p7 | 4:1058874 | TGAGCATCTGGAGCA[C/T]GAGCTTCCTCCCCCG | 285498 |
| rs113099775 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095421 | ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs113101346 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1096417 | CAGCTCCACGGTCTC[A/G]GGATAGCGCACCTGG | 285498 |
| rs113107949 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095775 | ATGGTCTCAGCATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs113125575 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079132 | ACACAGGACCAACAT[A/G]GGACCAACACAGGGT | 285498 |
| rs113274096 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114633 | TAGAAAACTTAGAAT[G/T]ACGTATGGGCTGGGT | 285498 |
| rs113329622 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1103956 | TTCAAAGATAACATG[C/T]TGGCGTATGTAAATG | 285498 |
| rs113359730 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095834 | ATGGTCTCGGGATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs113361461 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1088813 | TACAATTTGGGCTGC[C/T]GCTTCAGAGGGAGCA | 285498 |
| rs113396403 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079165 | ACACAGGACCAACAT[A/G]GGACCAACACAGGGT | 285498 |
| rs113406672 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1094631 | TCAGCTGCCAGAAGG[A/G]GGGCCCACGGAGCCA | 285498 |
| rs113410081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1104910 | AGAACACAGGTGCAC[A/G]TCATGAGGCATTTGA | 285498 |
| rs113463570 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096056 | CCCCCCACAGCTCCA[C/T]GGTCTCGGGATAGCG | 285498 |
| rs113476791 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095598 | ATGGTCTCAGCATAG[C/T]GCACCTGGCTCATCA | 285498 |
| rs113521083 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1099575 | GAAAACTGAATTTTT[A/G]TTAGACTTTTAAAAG | 285498 |
| rs113553785 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RNF212 | GRCh38.p7 | 4:1080131 | CACGCTCGGTACGCA[C/G]TAGTTCCTTCATTTG | 285498 |
| rs113555082 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079254 | CACAGGGTCAACACA[A/G]GACCAACATGGGACC | 285498 |
| rs113594203 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | RNF212 | GRCh38.p7 | 4:1089689 | GTCAAGGGAGGGATC[C/T]GGTGGGAAGTGATTG | 285498 |
| rs113600875 | snp | C/G | 0.5 | 0 | intron-variant, missense | RNF212 | GRCh38.p7 | 4:1099730 | CAGCGTGACTGAAGG[C/G]CTTTGCTGCGTCTGA | 285498 |
| rs113643775 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1069986 | AATTACGGGTGGTTT[C/G/T]GTAGGATTGCGCTGT | 285498 |
| rs113683134 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1109022 | AGCCTTTTTTTTTTT[C/T]TTTGAGACAGAGTTT | 285498 |
| rs113708827 | snp | A/G | 0.00016818 | 0.00916853 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1113312 | TTCCCTGACCCCCTT[A/G]CCGCTCCCCTCCCCT | 285498 |
| rs113782802 | snp | C/T | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095632 | AACCAAGCACACCCC[C/T]CACAGCTCCATGGTC | 285498 |
| rs113867503 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1079089 | CACAGGGTCAACACA[A/G]GACCAACATAGGACC | 285498 |
| rs113881125 | snp | A/G | 0 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1082010 | CATCCCAACACTTTG[A/G]GAGGCAGGGGCGGGA | 285498 |
| rs113958078 | snp | A/G | 0.5 | 0 | intron-variant | RNF212 | GRCh38.p7 | 4:1095851 | CACCTGGCTCATCAC[A/G]GAACCAACCACACCC | 285498 |
| rs114038957 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF212 | GRCh38.p7 | 4:1057579 | ACACACTGCCTGCCC[C/T]GGCCTTCTCAATACA | 285498 |
| rs114112762 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114317 | TTTTATAAAATTGTC[C/T]TCTGCGTGGTTTTGA | 285498 |
| rs114160701 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1077902 | CCGGTGGGTGTGGGC[A/G]TGGCCATGAGGATGG | 285498 |
| rs114174358 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF212 | GRCh38.p7 | 4:1097772 | GCCGTGAGCTAGAAT[C/T]GCTTGAGCAGTCCAA | 285498 |
| rs114395790 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1076675 | TCCAAAGGAACTGCT[A/C]CACACATCCACTCCA | 285498 |
| rs114478989 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1079749 | CTCTAACAACGTCAG[C/T]TGAAATACACACATG | 285498 |
| rs115015945 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1109711 | TCATGACCTACCTCA[A/G]TTTCTCTGCCCTCTC | 285498 |
| rs115072543 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | RNF212 | GRCh38.p7 | 4:1081997 | GCCTCATGTCCATCA[A/T]CCCAACACTTTGGGA | 285498 |
| rs115140555 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114353 | TCCACCCGCTGGGAC[A/G]CTGCAAAGCTCGGAT | 285498 |
| rs115191370 | snp | C/G | | | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1094050 | TTCAGAAGCAAGGAA[C/G]CTCCCAGAGGAGGAC | 285498 |
| rs115207016 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1110090 | ATTAACAGAGCCGAC[C/T]CATAAAAATCGAAAA | 285498 |
| rs115219588 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | RNF212 | GRCh38.p7 | 4:1094630 | CTCAGCTGCCAGAAG[C/G]GGGGCCCACGGAGCC | 285498 |
| rs115510208 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | RNF212 | GRCh38.p7 | 4:1066261 | TTCTCTAACGATGAA[C/T]GATGAGTATCTTTTC | 285498 |
| rs115523265 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF212 | GRCh38.p7 | 4:1098760 | GCACCCCCTCAGCCC[C/T]GGCCATGGCAAGTAG | 285498 |
| rs115529949 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF212 | GRCh38.p7 | 4:1061547 | AGTGATGCCACAGGG[A/G]ACCAGGAACTGACTG | 285498 |
| rs115539413 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1074096 | GTGTGTGCTGGGCCC[C/T]GCTCTGTGCCCACCC | 285498 |
| rs115610563 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF212 | GRCh38.p7 | 4:1059033 | TGACGACTGAGTTCT[A/C]AAGCAACACCTGCTC | 285498 |
| rs115722303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1107386 | AAAAGGTAAATCACA[A/G]TAACACACATAGAAT | 285498 |
| rs115756303 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1057509 | GGCTGAGTCCAGCCT[C/G]CCACCTGTTTTTGTA | 285498 |
| rs115764266 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1084960 | TGTGACTGGCGTCAC[A/C]AGCTTCCCACAGGCC | 285498 |
| rs115862321 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF212 | GRCh38.p7 | 4:1110731 | GCTAAACAAGGGCTT[C/T]CCTCTGAGTGACACA | 285498 |
| rs115940263 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | RNF212 | GRCh38.p7 | 4:1060635 | TTCACAAAGATGTCC[A/C]TTTGAAAAATTTAAC | 285498 |
| rs115953578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1077962 | GTGTGCTTGACCCAA[C/G]TGCCAAGGAACTGGC | 285498 |
| rs115976848 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1064816 | CTTCCCACCCCTCCA[C/T]CCCACAGCCGCTGGC | 285498 |
| rs116148541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1084989 | CCCCACGGCCCCAGT[A/G]AGGCCATGCCATGCT | 285498 |
| rs116149773 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | RNF212 | GRCh38.p7 | 4:1080777 | GTCCAGGACCTGTAA[A/G]TAATAAATCTGAATG | 285498 |
| rs116254720 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | RNF212 | GRCh38.p7 | 4:1066157 | CCATCTCCTTGGCTC[A/G]AGCAATCCTCCCACC | 285498 |
| rs116273003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056596 | ATTTTAAAAAATTCA[A/G]ATGTCATCTTAGTAT | 285498 |
| rs116307182 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | RNF212 | GRCh38.p7 | 4:1104934 | CATTTGAGGATGGGT[G/T]CTGGGGGCTCCTCCC | 285498 |
| rs116355641 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | RNF212, LOC105374344 | GRCh38.p7 | 4:1113752 | TCTTGGCGGTCCTCA[A/G]GTGTTTTGTGGAAGC | 285498 |
| rs116365416 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1103327 | AAACATTTAAAGAAA[C/T]AACCCCCATCTTACA | 285498 |
| rs116446706 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF212 | GRCh38.p7 | 4:1074639 | TAACCTTGGAAGGAC[A/G]GACCCCCCTGCTTGG | 285498 |
| rs116456117 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF212 | GRCh38.p7 | 4:1059152 | CCTGCTGCGGCACGT[C/T]GGGGGGTTGCCGGCT | 285498 |
| rs116472927 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF212 | GRCh38.p7 | 4:1090026 | TGGGATGAGGGGTGA[C/T]GGGATGGGATGGGGT | 285498 |
| rs116547856 | snp | C/T | 0.0267878 | 0.112589 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058301 | ACGCAGTGAAGAAGG[C/T]GCTTGCGGGGGGGCA | 285498 |
| rs116596158 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | RNF212 | GRCh38.p7 | 4:1062857 | CTCATAAACTCAGTA[C/G]ATTGCAGGATACAAG | 285498 |
| rs116675283 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF212 | GRCh38.p7 | 4:1077657 | TGGAGGCTGTGAGTT[C/G]ATCCGTGAAACAAGG | 285498 |
| rs116676505 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058117 | AAACCTGACTCAAAG[C/T]GTGTAAAAACAGGGA | 285498 |
| rs116731314 | snp | A/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1064820 | CCACCCCTCCATCCC[A/C]CAGCCGCTGGCAGCC | 285498 |
| rs116765926 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | RNF212 | GRCh38.p7 | 4:1079498 | CAGCCCACCCCTCTC[A/C]CCCACGGGACCAGCA | 285498 |
| rs116787348 | snp | A/C/G/T | 0.0123139 | 0.0775937 | intron-variant | RNF212 | GRCh38.p7 | 4:1092010 | TCCCACCTTTGCCGA[A/C/G/T]GCTTCTCAAGTCCTG | 285498 |
| rs116845605 | snp | C/T | 9.88435e-05 | 0.00702937 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1073128 | AAATGACACACTCTC[C/T]GGGCACAGGGGGCTT | 285498 |
| rs117041041 | snp | A/G | 0.00404039 | 0.0447646 | intron-variant, synonymous-codon | RNF212 | GRCh38.p7 | 4:1093451 | ACGTCACACAGCTGC[A/G]GGAAAACTCCACCCT | 285498 |
| rs117097045 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF212 | GRCh38.p7 | 4:1101621 | AAATTCCACACCACT[C/T]GTGACATCATCTGCT | 285498 |
| rs117192583 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF212 | GRCh38.p7 | 4:1099117 | TCAGTGAGGCCTGAG[C/T]GGGAGAACACAGGCA | 285498 |
| rs117675054 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1071976 | GCACATGGACATCTA[C/T]AGCAGCTTAATTCAT | 285498 |
| rs117783335 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1060746 | CTGTGCTGTGTTCTG[A/G]AGGGGACCGCGTACT | 285498 |
| rs117856705 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF212 | GRCh38.p7 | 4:1101213 | CACAGTGCAGTAGCC[A/G]TGGTGGCATCTCTAC | 285498 |
| rs118112880 | snp | C/T | 0.342793 | 0.232141 | intron-variant, synonymous-codon, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093541 | GGGCAGAGCCTGTGA[C/T]CTCCACGGCCCATGC | 285498 |
| rs137960323 | snp | C/T | 6.62306e-05 | 0.00575421 | missense, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1079668 | GGAGAAGGAGAGAGA[C/T]CAACTTCCATCGACT | 285498 |
| rs137978316 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1092164 | CAGCTTCACATGTTC[A/G]TGGAGGAACCTACCA | 285498 |
| rs138087667 | snp | C/G | 0.0554779 | 0.157039 | intron-variant, upstream-variant-2KB | TMED11P, LOC105374344, RNF212 | GRCh38.p7 | 4:1115652 | GAATTTGACCTATTC[C/G]TATATTTTATTTGCT | 285498 |
| rs138146107 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF212 | GRCh38.p7 | 4:1075762 | CTCACTGCAGCCTCA[A/G]CCTCCTGGTGGTGAT | 285498 |
| rs138241686 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1114340 | GGTTTTGAGAGTTTC[C/T]ACCCGCTGGGACGCT | 285498 |
| rs138292229 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF212 | GRCh38.p7 | 4:1064756 | CTCTATAACTGTTTT[C/T]ATTTTGTGAAACTGA | 285498 |
| rs138354733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1100757 | AACAAATGGTCTCTA[A/T]CATCATATTTGACCA | 285498 |
| rs138488801 | in-del | -/CTGCCCAGGCTGGAGCCAGCC | 0.350109 | 0.229081 | intron-variant, cds-indel, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093539 | TGGGCAGAGCCTGTG[-/CTGCCCAGGCTGGAGCCAGCC]ACCTCCACGGCCCAT | 285498 |
| rs138490360 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056209 | TTAAGGAAGTTCCAA[A/G]TTAAGAGTAAAGTTG | 285498 |
| rs138539593 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1068492 | GTTGCTCCATCTCCT[C/T]GCTCTTCCTTTGTGC | 285498 |
| rs138699291 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1083504 | AAAAATCAGCCAGGC[A/G]TGGTGGGGCTGTAAT | 285498 |
| rs138737687 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1104987 | TGCAGCTCTGCCTTC[C/T]GGAGGAGCTCTCTTG | 285498 |
| rs138766682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1108258 | CTGAAAATTTTAGAC[A/G]CCACAAATGACTAAA | 285498 |
| rs138831120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1078653 | GGCAGTTAAAGCCCA[C/G]GGCCACCAACTTTGC | 285498 |
| rs138906288 | snp | A/C/T | 0.0740172 | 0.177567 | intron-variant, utr-variant-5-prime | RNF212 | GRCh38.p7 | 4:1099821 | GTCCACAAGGTCCGA[A/C/T]GGCGCAAGCGGACAC | 285498 |
| rs138937836 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1060932 | TTGTTGAGGAGGACT[G/T]CTGGCTACAGTGGAG | 285498 |
| rs139028047 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | RNF212 | GRCh38.p7 | 4:1092725 | GGCTGCGCTGGGCCA[C/G]GTCAGCCCAGGGCCC | 285498 |
| rs139283815 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF212 | GRCh38.p7 | 4:1057431 | GCAGCAGACGGAGTG[A/G]GAGGCCACCCAGAGG | 285498 |
| rs139285565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1105710 | CACGGATGCACCCAC[A/G]TGCAAGTGCACATGC | 285498 |
| rs139291604 | snp | A/C | 0.00029969 | 0.0122375 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1108385 | AGGAGCTTTACAAAT[A/C]AAGCATTCATTCTTT | 285498 |
| rs139353698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1109658 | TGGGGCTGCTCAAAC[C/T]AGGGCCCTCATATCA | 285498 |
| rs139353780 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF212 | GRCh38.p7 | 4:1066622 | AAGTGTGCACCACTG[C/T]GCCCAGGCTTTGCCC | 285498 |
| rs139484315 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1106744 | TGCGAGGGTACCGTG[A/C]GAGGAGCAGAAGCAG | 285498 |
| rs139595779 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1101872 | TATGATTCTGAAAAA[C/T]TGACTGAGGTATACA | 285498 |
| rs139634820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1090274 | AAGGGTGATCTGTCC[A/G]CTCCAGGTTTGGGTG | 285498 |
| rs139725124 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant, missense | RNF212 | GRCh38.p7 | 4:1094212 | GGTGGGGTGGCCAAC[A/G]GTGGGAGCTGCACTC | 285498 |
| rs139785280 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RNF212 | GRCh38.p7 | 4:1057835 | CTTGGGAGGCCGAGG[A/C]AGGCAGATCACCTGA | 285498 |
| rs139872801 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072055 | GATGAACTATGATAC[A/C]TCCAGATAATGGAAT | 285498 |
| rs139919196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1097163 | AGGCCTCCAGCCCAG[C/T]CTCCTCCTTTAGTAT | 285498 |
| rs139934742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1076472 | AATGCTCTTTCCCAT[G/T]CAGCCCTGAACAGTG | 285498 |
| rs140128337 | snp | A/G | 0.000131776 | 0.00811608 | missense, utr-variant-5-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1096832 | AATGCCTGGATATCT[A/G]CGTCGGTCTGAAAGA | 285498 |
| rs140154714 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF212 | GRCh38.p7 | 4:1083868 | TTTACAGAACTGATG[C/T]AAAACACGAATCCAC | 285498 |
| rs140161476 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1089636 | GGTTTGGCTCTGTGT[C/T]CCCACCCAAATCTCA | 285498 |
| rs140257626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1098813 | GTGCCCCCAGCAGAG[C/T]GTGGCCCATGTGAGT | 285498 |
| rs140263650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1059246 | CCCCGGGGCTGTGCA[C/G]ACCTTGTGAGGATGC | 285498 |
| rs140326541 | in-del | -/CTTGCTGCAGTGGGATAAC | 0.244987 | 0.24995 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1094050 | TCAGAAGCAAGGAAG[-/CTTGCTGCAGTGGGATAAC]CTCCCAGAGGAGGAC | 285498 |
| rs140555209 | snp | A/G | 0.000136505 | 0.00826037 | intron-variant | RNF212 | GRCh38.p7 | 4:1081627 | ATCTCATACTAAATA[A/G]ATGGAGAAAAGGTAT | 285498 |
| rs140567472 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF212 | GRCh38.p7 | 4:1084205 | ATCTGCCCACCTTGG[C/T]CTCCCAAAGTGCTGG | 285498 |
| rs140571523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1077720 | TGTCTGGCCTTGGGG[G/T]AGCCAAAGCAGGTGG | 285498 |
| rs140575820 | in-del | -/T | 0.269267 | 0.249256 | intron-variant | RNF212 | GRCh38.p7 | 4:1089706 | TGGGAAGTGATTGGA[-/T]TCATGGGGGCAGTTT | 285498 |
| rs140588441 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF212 | GRCh38.p7 | 4:1064319 | CACCTCAGTGAGTGT[C/T]CACTGTGGTGAGTTC | 285498 |
| rs140745306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1062692 | AAAGTCCTGCAGTGG[A/G]ACGGGAAGTGAAAAG | 285498 |
| rs140852359 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF212 | GRCh38.p7 | 4:1067720 | ATTACAAAAATTAGC[C/T]GGGTGAGGTGCTGCA | 285498 |
| rs140928446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1085536 | GAAAGCAGGCAGCCA[A/G]GCTGCAGGTGGAGTC | 285498 |
| rs141035079 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | RNF212 | GRCh38.p7 | 4:1081193 | CAAACCAATCACTGT[C/T]GCTGCAGGATGGAGT | 285498 |
| rs141310035 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | RNF212 | GRCh38.p7 | 4:1091953 | GCAGGTTGCCCTGAC[A/C]CCAGCTCTTGTGCAC | 285498 |
| rs141381105 | snp | C/T | 0.000593893 | 0.0172219 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1073639 | AATCATGGAGATTCT[C/T]GCAGGGCCGGCTGCT | 285498 |
| rs141420667 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF212 | GRCh38.p7 | 4:1107862 | AATCATCAGACCAAA[C/T]GCACATTTTGGAGAT | 285498 |
| rs141626885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1089021 | CAGAAGGGAAATGTG[C/T]GGTGGTTGTTCCCAC | 285498 |
| rs141736607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMED11P, LOC105374344, RNF212 | GRCh38.p7 | 4:1115680 | GCTACCATCAGGCAA[A/G]GCGAATATTACCCAA | 285498 |
| rs141760100 | snp | G/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1104095 | CTTGAGAAAAATTGT[G/T]TAAAACTACAATAGT | 285498 |
| rs141767469 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF212 | GRCh38.p7 | 4:1105575 | AGGTCTGGGGAAGTC[C/T]ACTTACAATGTGTTT | 285498 |
| rs141837552 | in-del | -/G | 0.144969 | 0.226867 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1058307 | GAAGAAGGTGCTTGC[-/G]GGGGGGGCACTACCT | 285498 |
| rs141935801 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF212 | GRCh38.p7 | 4:1078729 | GGGACCAACATGGGA[C/T]CAGCAGAGGATCAAC | 285498 |
| rs141944410 | snp | C/T | 0.000153834 | 0.00876889 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093726 | AACAGACATGTTTTA[C/T]GAACTCAAGCAACTT | 285498 |
| rs142050215 | in-del | -/TG | | | intron-variant | RNF212 | GRCh38.p7 | 4:1070368 | TTTGTAGGGCTGTGC[-/TG]TGTCAGCGTGGGTGC | 285498 |
| rs142073400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1110250 | AGGCTATGAGGAGAC[C/G]TGAATAGGCATAGGA | 285498 |
| rs142132776 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072154 | TGCTAAGTGAAAGGA[A/G]TCAATCTGAGAAGCC | 285498 |
| rs142148366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1089834 | GACGTGCCTTGCTTC[C/T]CCTTTGCCTTCTGCC | 285498 |
| rs142176103 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1086105 | TCTGCCTGGAGTTCC[A/G]CCCATCAGACACTTA | 285498 |
| rs142187515 | snp | C/T | 0.00914975 | 0.0670161 | missense, utr-variant-5-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1096836 | CCTGGATATCTGCGT[C/T]GGTCTGAAAGAGAAA | 285498 |
| rs142214972 | snp | C/G/T | 0.00637319 | 0.05614 | intron-variant | RNF212 | GRCh38.p7 | 4:1092756 | CAAGGAAGAGCTGCC[C/G/T]GGTGCTCACGCGTGC | 285498 |
| rs142228667 | snp | A/G/T | 0.000148335 | 0.00861078 | RNF212 | 4 | allele_origin=G(germline)/A(somatic) | 4:1072982 | GAACGGAAACAAGAC[A/G/T]GCCCTTTGTACCTCA | 285498 |
| rs142232513 | snp | C/G | | | intron-variant, stop-gained, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093539 | CTGGGCAGAGCCTGT[C/G]ACCTCCACGGCCCAT | 285498 |
| rs142237919 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1066388 | GGCTGGAGTGCAGTG[C/G]CACAATCTCGACTTA | 285498 |
| rs142241392 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF212 | GRCh38.p7 | 4:1091582 | TCCACCTTGCCATCT[A/G]CGATGATAACACAAG | 285498 |
| rs142250296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1091218 | AGCCGGCACACAGAA[C/T]GAGGCTAAGCGAGAC | 285498 |
| rs142327619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1060273 | ATGGGATCTCAGACC[C/T]GAAAGACCCCTGCCG | 285498 |
| rs142496855 | in-del | -/ATTACCTG | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1073872 | GGTGGGTATTACCTG[-/ATTACCTG]TTTGATTCCCTCTGT | 285498 |
| rs142516789 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1107498 | TCTCGCTCAGTCACC[C/T]AGGCTGGAGTGCAGT | 285498 |
| rs142551226 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF212 | GRCh38.p7 | 4:1109720 | ACCTCAATTTCTCTG[C/T]CCTCTCCTCTAGACT | 285498 |
| rs142580978 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111987 | GGCCAAGGCCGGTGA[C/T]TGTTAGAGGACAGGA | 285498 |
| rs142582825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1068498 | CCATCTCCTCGCTCT[C/T]CCTTTGTGCTTATTA | 285498 |
| rs142594077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1073798 | CTCTGACAAGTTCCT[C/G]TCTAACTTGATTCTG | 285498 |
| rs142629458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1076025 | TGAGTCATGATTTTA[C/T]CTTTTCAAAAAGATA | 285498 |
| rs142685900 | in-del | -/C | 0.0441095 | 0.141807 | intron-variant | RNF212 | GRCh38.p7 | 4:1068047 | GCAATTCTCCCCACA[-/C]CCGATGTAGAGATTC | 285498 |
| rs142698097 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | RNF212 | GRCh38.p7 | 4:1083511 | AGCCAGGCGTGGTGG[G/T]GCTGTAATCCCAGCT | 285498 |
| rs142729351 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1101473 | ATGGGATTTTGTTCA[A/T]CTGCTCCTGTTGAAG | 285498 |
| rs142733201 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1087818 | TTTAAAAGTGTTTGG[C/T]AGTTCCCCTCCACCC | 285498 |
| rs142878453 | in-del | -/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096989 | GGGGCCCTGCCAGGG[-/C]ACAGCCTCGATCAAC | 285498 |
| rs142934796 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RNF212 | GRCh38.p7 | 4:1080950 | CCTGGAGATGGGGCA[A/G]ACACAAGCCACAGGA | 285498 |
| rs142952416 | in-del | -/AG | 0.290977 | 0.246619 | intron-variant | RNF212 | GRCh38.p7 | 4:1098186 | GGACAGTGAGCGCAT[-/AG]AGAGTCAAGACAGTC | 285498 |
| rs143003795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1092238 | GTTCTTAGAGAAAGG[C/T]CTTGGGGAGACGAGG | 285498 |
| rs143004542 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1064076 | CCCTGCAAGAAAAAA[C/T]TGGAAATGGTTAATA | 285498 |
| rs143009328 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1065587 | ATTCTCCCACCTCAG[C/T]ATCCTGAGAAGCTGG | 285498 |
| rs143046808 | snp | A/C | 0.00829582 | 0.0638678 | missense, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1081619 | TTGTGATGATCTCAT[A/C]CTAAATAGATGGAGA | 285498 |
| rs143127061 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1058827 | GGCAGCTGTGGGCAT[A/G]CGGACTGTGCCTGGC | 285498 |
| rs143367453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1102057 | TCAAATACATATACT[A/G]CAGGCAAAAATGAAC | 285498 |
| rs143417573 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1103106 | ATGAAAAATATGAGT[G/T]GATAACAAGCATATT | 285498 |
| rs143430357 | in-del | -/GAA | | | intron-variant | RNF212 | GRCh38.p7 | 4:1060114 | AAAAAAAAAAAAAAA[-/GAA]AAAAGAAATTGTTTC | 285498 |
| rs143462127 | in-del | -/TGC | | | intron-variant | RNF212 | GRCh38.p7 | 4:1110271 | AGGCATAGGAAAAAA[-/TGC]AAACAGCCAATAAAC | 285498 |
| rs143488908 | snp | C/G/T | 0.0256316 | 0.110334 | intron-variant | RNF212 | GRCh38.p7 | 4:1079514 | CCCACGGGACCAGCA[C/G/T]ACGAAGCAGCAGCAC | 285498 |
| rs143489494 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF212 | GRCh38.p7 | 4:1088584 | AGCTGGCTGCAGAAA[C/T]GTGCATAAGTAACCA | 285498 |
| rs143560516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1082392 | GGGGAGCGTGTCTGT[C/T]TCTGTGGACACACTG | 285498 |
| rs143624209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1082718 | AAGCTCCCAGAGGAC[A/G]GGCACTGGGCGTGTT | 285498 |
| rs143700023 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime, splice-donor-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113647 | GGGTTCTCCCGCAGC[A/G]CCTGGGAGGGCGCGT | 285498 |
| rs143723235 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF212 | GRCh38.p7 | 4:1081221 | AGTGCTCTGATTGGC[C/T]ACCTGGATCACACAC | 285498 |
| rs143734193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1075292 | GCCATTCTTGCACTG[C/T]GATAAATACCAGAGA | 285498 |
| rs143788959 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF212 | GRCh38.p7 | 4:1084053 | TCCCAAGTTCAAGAG[A/G]TTCTCCTGCCTCAGC | 285498 |
| rs143834997 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1068384 | ACACATGCTTTACAA[C/T]GTCATGTAAAAATCC | 285498 |
| rs143895688 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF212 | GRCh38.p7 | 4:1104879 | AAACACTCCCCACCA[C/T]ACCAAGGGAGGAGGA | 285498 |
| rs143896663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1061872 | CAGTACCCAGGTTGT[C/T]CAGATTGCAGCCCCA | 285498 |
| rs143956184 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1109852 | ACTCGCCTCAGTGTC[C/T]GCAGCTCCCAGCACA | 285498 |
| rs143972784 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF212 | GRCh38.p7 | 4:1065078 | CATGTTTTAGACACT[A/G]TGAATAATACTGCTA | 285498 |
| rs144058059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1106169 | TTCGGAAGACACTGC[A/G]GAAGAAAGAGCCCAC | 285498 |
| rs144092139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1066634 | CTGCGCCCAGGCTTT[A/G]CCCATTTTTGAATCA | 285498 |
| rs144107912 | in-del | -/CT | 0.0123036 | 0.0774623 | intron-variant | RNF212 | GRCh38.p7 | 4:1074247 | CTGAGCCCCTCCTGC[-/CT]CTCAGTGCGACCTGG | 285498 |
| rs144160971 | in-del | -/CAG | | | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1092990 | AAACTACGCCAGGAC[-/CAG]GGTCTGCGTGCTCAG | 285498 |
| rs144215622 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1084596 | TTAGCTGTGTGTGGT[G/T]GTGCGTGCCTGTGGT | 285498 |
| rs144377673 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF212 | GRCh38.p7 | 4:1083688 | AACTCAGTGGGGTTC[A/G]CTGGCTTAACCTGAA | 285498 |
| rs144399534 | in-del | -/TGATCAC | | | intron-variant | RNF212 | GRCh38.p7 | 4:1065530 | GGGGTGCAGTGGTAT[-/TGATCAC]GATCACTGCTCACTG | 285498 |
| rs144516527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1076596 | ACCTCTGCTCAGGCT[A/G]AGGGTTACCAGGAGC | 285498 |
| rs144615831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1063219 | TGATCCTAAAATTCA[C/T]ATGGAAATGCAAGGA | 285498 |
| rs144654020 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF212 | GRCh38.p7 | 4:1065916 | GGATCTTACTCTGTC[A/G]TCCAGGCTGGAGTGC | 285498 |
| rs144680141 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1094739 | TGTCAAGAAGCAACC[-/T]GCTGCCCTGAACCCA | 285498 |
| rs144741839 | in-del | -/AT | | | intron-variant | RNF212 | GRCh38.p7 | 4:1064815 | GCTTCCCACCCCTCC[-/AT]CCCACAGCCGCTGGC | 285498 |
| rs144952826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1077280 | ACAGAAAATGCCCAT[A/G]TCTGGTCTTTGCCCC | 285498 |
| rs144983110 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1097760 | AGGCATGGAGCTGCC[A/G]TGAGCTAGAATCGCT | 285498 |
| rs145003816 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF212 | GRCh38.p7 | 4:1078403 | TGGTGTGTGGCCGAT[A/G]TGGTACATCTGGCGC | 285498 |
| rs145079835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1085835 | CTTGGAGAGCCAGAC[A/G]ACCAATGCACATGGC | 285498 |
| rs145201140 | snp | C/T | 0.0337553 | 0.125452 | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1055856 | GGCTCTGAGACTCTC[C/T]GGGAGCCACGTGCAC | 285498 |
| rs145237365 | snp | A/G | 5.01132e-05 | 0.0050054 | intron-variant | RNF212 | GRCh38.p7 | 4:1090886 | AGATCCACGGTCTCT[A/G]TGGCTGGAGTTTTGT | 285498 |
| rs145249080 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | RNF212 | GRCh38.p7 | 4:1077948 | CAGGGAGAGGATGCG[A/T]GTGCTTGACCCAACT | 285498 |
| rs145316354 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF212 | GRCh38.p7 | 4:1057855 | AGATCACCTGAGGTC[A/G]GGAGTTCGAGACCAG | 285498 |
| rs145351016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1057472 | GCAGGGGGAGGTGAA[C/T]TGTGGTCTGTTCCGG | 285498 |
| rs145441558 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1068300 | GAAGAAAGCCCTCAC[A/T]GGCCGTTCTGCTATT | 285498 |
| rs145516890 | in-del | -/TTTATCTCATCCTAA | 0.349233 | 0.229462 | intron-variant | RNF212 | GRCh38.p7 | 4:1066057 | CCATCCTAATGGCTG[-/TTTATCTCATCCTAA]TGAGATACTATCTTG | 285498 |
| rs145602858 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF212, TMED11P, LOC105374344 | GRCh38.p7 | 4:1115113 | CAGAAGCTGCATTAT[A/G]AAAGCATTCTCTCAA | 285498 |
| rs145617430 | snp | A/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1081702 | TGAAAGTGTAAGAAG[A/G]CTCTGAATCAGTGAA | 285498 |
| rs145692089 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111968 | CTAATCCCACATTTC[A/G]GGAGGCCAAGGCCGG | 285498 |
| rs145764708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112471 | CTTGCATAAACATCA[A/G]TTCAACACAAAATTT | 285498 |
| rs145863700 | in-del | -/AGG | 0.0174175 | 0.0916809 | intron-variant | RNF212 | GRCh38.p7 | 4:1074778 | GAATCTTGTGAAATC[-/AGG]AGCTTTTGTCTCTGT | 285498 |
| rs145908659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1086204 | GCACCCCACACAAGC[C/T]GGCAGGATGCAAATT | 285498 |
| rs145921632 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096528 | CCCCCCACAGCTCCA[C/T]GGTCTCAGGATAGTG | 285498 |
| rs145986957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1091722 | CCCAACCTCCTCCAT[A/G]AGAGGCCATCTCCAG | 285498 |
| rs145990706 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1071692 | CTCCTAGTCATATGT[C/T]ATCAATGAAATGCAA | 285498 |
| rs146025515 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1076451 | CCCACCAAGAGCACC[A/C]CCGATAATGCTCTTT | 285498 |
| rs146148253 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1056685 | AAGTGAACATTACTG[C/T]GTTTCTGAACAACTA | 285498 |
| rs146161994 | snp | C/T | 0.000131781 | 0.00811621 | missense, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1096804 | CTTACACAGACTGTC[C/T]ATGCTCATGAAGAAT | 285498 |
| rs146228753 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073054 | CCTTCCAGAACTGAA[C/T]GCTAGGAGGAGCAGC | 285498 |
| rs146232342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1105686 | ACTGATTTCACCGAA[A/G]TGCTCACACACGGAT | 285498 |
| rs146265365 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF212 | GRCh38.p7 | 4:1109345 | ATCTTAATCTAAAAT[A/T]TTTAACTATTCAAAA | 285498 |
| rs146390047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RNF212 | GRCh38.p7 | 4:1093394 | AAATGCCAATATTTA[C/T]GTTACGTTGATATTA | 285498 |
| rs146455535 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1066657 | TTGAATCAGGTTGTT[C/T]GTTGTTAAGTTTTAG | 285498 |
| rs146522961 | in-del | -/CC | 0.0341408 | 0.126114 | intron-variant | RNF212 | GRCh38.p7 | 4:1061682 | AAAGACAGGCGGACA[-/CC]CCCCGGGACATCTCA | 285498 |
| rs146635352 | in-del | -/C | | | intron-variant | RNF212 | GRCh38.p7 | 4:1096990 | GGGCCCTGCCAGGGA[-/C]CAGCCTCGATCAACA | 285498 |
| rs146684160 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | RNF212 | GRCh38.p7 | 4:1069044 | GAAACTCCATCTCTA[C/G]TAAAAATACAAAAAC | 285498 |
| rs146698366 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | RNF212 | GRCh38.p7 | 4:1102352 | ACAGTTGGCCTTGTA[G/T]AACCTGCATACAGGA | 285498 |
| rs146814980 | snp | A/C/G | 0.000280375 | 0.0118369 | missense, synonymous-codon, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1081457 | TGGCAGCAGGCATCC[A/C/G]TGTGGTTTTGCTGGA | 285498 |
| rs146818304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1073980 | TTGCAGCTGATGTTA[A/G]AGAATGTGAAATTCT | 285498 |
| rs146994272 | snp | A/T | | | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093536 | TCACTGGGCAGAGCC[A/T]GTGACCTCCACGGCC | 285498 |
| rs147076385 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF212 | GRCh38.p7 | 4:1104407 | GGCTCAGGTCACCCC[A/G]CCCCCAGCAGCTCTG | 285498 |
| rs147162763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1079566 | TGCACGAGAGGTTAC[A/G]TTTTTCACTACTGAG | 285498 |
| rs147176544 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF212 | GRCh38.p7 | 4:1083494 | CTAAAAATACAAAAA[C/T]CAGCCAGGCGTGGTG | 285498 |
| rs147238314 | snp | C/T | | | intron-variant | RNF212 | GRCh38.p7 | 4:1101203 | GACTGGCACTCACAG[C/T]GCAGTAGCCGTGGTG | 285498 |
| rs147268978 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1062662 | GAGAGGGCGGTTAGG[C/T]GAGAAAAACAAATGA | 285498 |
| rs147285678 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF212 | GRCh38.p7 | 4:1065471 | CCATTCTCCTCTCTC[A/G]TTTTCTTTTTTCTTG | 285498 |
| rs147477708 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF212 | GRCh38.p7 | 4:1097049 | TCTGAGGGCTGTGCC[A/G]GACAGTGGTGAGGGC | 285498 |
| rs147493640 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF212 | GRCh38.p7 | 4:1100660 | GTGATCTGCCCGCCT[C/T]GGCTTTGCAAAGTGC | 285498 |
| rs147538043 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF212 | GRCh38.p7 | 4:1080611 | CTGCTCTAAACCCAC[C/T]AATTAAAACTCCTCA | 285498 |
| rs147555569 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF212 | GRCh38.p7 | 4:1077176 | GAGGTTGCAGTGAGC[C/T]GAGATCTCGCCACTG | 285498 |
| rs147660635 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1057595 | GGCCTTCTCAATACA[A/G]AGGTGGAGCTGAGCA | 285498 |
| rs147728427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1107378 | TTTTTATGAAAAGGT[A/G]AATCACAATAACACA | 285498 |
| rs147745139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1111981 | TCGGGAGGCCAAGGC[C/T]GGTGATTGTTAGAGG | 285498 |
| rs147747822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF212 | GRCh38.p7 | 4:1073749 | CTGTTAGGAACACAT[A/T]TCCCAGAACCCCATC | 285498 |
| rs147818050 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073084 | CCAGTGAGGACAGAC[A/G]TCTATGCAGAAACAT | 285498 |
| rs147832922 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1091950 | TCCGCAGGTTGCCCT[C/G]ACCCCAGCTCTTGTG | 285498 |
| rs147849078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1094903 | AACAATAAAACAGAC[C/G]AAATGAACATTGTCA | 285498 |
| rs147955506 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF212 | GRCh38.p7 | 4:1077661 | GGCTGTGAGTTCATC[C/T]GTGAAACAAGGCCCT | 285498 |
| rs148043584 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF212 | GRCh38.p7 | 4:1082492 | TTTGAGATACGAACA[A/G]TCTGCCCTCAGCAGT | 285498 |
| rs148110414 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1075306 | GCGATAAATACCAGA[C/G]ACTGTGTAATTCATA | 285498 |
| rs148172320 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF212 | GRCh38.p7 | 4:1099337 | AATAAAGGAATTCCC[C/T]GTAGGTAAGAAAAAT | 285498 |
| rs148209783 | snp | C/T | | | intron-variant, synonymous-codon, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093538 | ACTGGGCAGAGCCTG[C/T]GACCTCCACGGCCCA | 285498 |
| rs148323317 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1107853 | TTATATTTAAATCAT[C/G]AGACCAAATGCACAT | 285498 |
| rs148376946 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF212 | GRCh38.p7 | 4:1064172 | CAGGAAATAATGACA[A/C]CACCATATTGTTAGA | 285498 |
| rs148418544 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | RNF212 | GRCh38.p7 | 4:1076703 | CCAGGGTGACAAGGC[A/G]TTTCGGGAGGTGAAA | 285498 |
| rs148485974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1101430 | GTTCTGAAAGGTCCT[A/G]TAAACATGGTATTCC | 285498 |
| rs148539340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1061723 | AAAAGAGCAGAAACC[A/G]TGAGCGGACACATCT | 285498 |
| rs148573001 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1080733 | CTACCTGTGGACAGA[A/G]CACTGTCCTCCCCAC | 285498 |
| rs148625459 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF212 | GRCh38.p7 | 4:1109989 | CTTGACAGTAGGTCC[C/T]CTCCCTTCTAGCTCT | 285498 |
| rs148680470 | snp | C/G | | | intron-variant | RNF212 | GRCh38.p7 | 4:1105516 | CCAGGTCAAGGAACA[C/G]AGCGTCAGAGGGTCA | 285498 |
| rs148727567 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | RNF212 | GRCh38.p7 | 4:1090951 | AGCTCACAGTGCTTG[A/T]CTTACGTGTGTCCTG | 285498 |
| rs148820241 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF212 | GRCh38.p7 | 4:1068304 | AAAGCCCTCACTGGC[C/T]GTTCTGCTATTTATT | 285498 |
| rs148945469 | snp | A/G | 0.0325976 | 0.123435 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | RNF212, LOC105374344 | GRCh38.p7 | 4:1113528 | GCAAGGTTGGGACCA[A/G]CCTCCCCGCGCAGGG | 285498 |
| rs148974956 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1074390 | GTCCTCAGGCTCTGC[C/T]GCCATCAACTGTGCC | 285498 |
| rs149082351 | snp | G/T | 0.0748431 | 0.178382 | intron-variant | RNF212 | GRCh38.p7 | 4:1098009 | GGTGGAGGTTGCAGT[G/T]AGCCGAGATCATGCC | 285498 |
| rs149097918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1058721 | TGGATAGCAAGACCT[A/G]GAAACGAACTGGCCA | 285498 |
| rs149157258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1078327 | TCCCTCCTATGGGGT[A/G]CAGCTCACTCTGCCC | 285498 |
| rs149255928 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1055768 | TTTAGGTAAATGCAA[A/T]CTAAAAGATTAGAAC | 285498 |
| rs149297104 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1076576 | GCAACAGGTGGTGTC[A/C]CAGAACCTCTGCTCA | 285498 |
| rs149350433 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF212 | GRCh38.p7 | 4:1105267 | GCAGATGCAGGGGGA[A/G]CACAGCTGCTGCTCT | 285498 |
| rs149460349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1092188 | CCTACCAGCAGACGC[A/G]CCTCATCCCGGCTGT | 285498 |
| rs149485506 | snp | C/G/T | 0.00655876 | 0.0568912 | missense, intron-variant, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1081428 | ACACACCTGTCGGGG[C/G/T]CTGATGAGTGAGGTG | 285498 |
| rs149561628 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF212 | GRCh38.p7 | 4:1070182 | GGACGCCTGGCCTGA[A/G]TTGTGGGTGGTTTTG | 285498 |
| rs149655587 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF212 | GRCh38.p7 | 4:1106802 | ATGTGTGGAGGAAAA[C/G]AAAGTATTTTCTGTT | 285498 |
| rs149671814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1067969 | TGAGAGAAACTAAAG[A/C]AGCTCTAATCAATGG | 285498 |
| rs149815059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF212, LOC105374344 | GRCh38.p7 | 4:1112170 | CGAGATCCCGCCACC[A/G]AACTCCAGCCTGGGC | 285498 |
| rs149876577 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073404 | CTGTGACTTGTTACA[C/T]GGTCATCAGGAGCTT | 285498 |
| rs149936894 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | RNF212 | GRCh38.p7 | 4:1097663 | TCAGGATGCCCTGCC[A/T]CACCTCCCTGCACCT | 285498 |
| rs150070315 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | RNF212 | GRCh38.p7 | 4:1083672 | AACAAACAAACAAAC[A/T]AACTCAGTGGGGTTC | 285498 |
| rs150266301 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1099696 | TGGTACAGTAACGAG[A/G]ATACATAGTTAAATC | 285498 |
| rs150320559 | snp | A/G | 3.30071e-05 | 0.00406232 | missense, utr-variant-3-prime, nc-transcript-variant | RNF212 | GRCh38.p7 | 4:1073640 | ATCATGGAGATTCTC[A/G]CAGGGCCGGCTGCTA | 285498 |
| rs150335639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1092136 | CACCCTGCAGGCAAG[C/T]GCCTCTGCTTCTCAG | 285498 |
| rs150340270 | in-del | -/TTTTT | | | intron-variant | RNF212 | GRCh38.p7 | 4:1100421 | TTTTTTTTTTTTTTT[-/TTTTT]GAGATGGAGTCTTAC | 285498 |
| rs150384251 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1085773 | AAAGTTTCTGGTAAA[C/T]GAACGAGCTCTTCCC | 285498 |
| rs150390954 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF212 | GRCh38.p7 | 4:1108212 | ACTGCATTTTGATTA[C/G]TCAGATATCTTTGTT | 285498 |
| rs150414849 | in-del | -/AG | 0.0205511 | 0.0992634 | intron-variant | RNF212 | GRCh38.p7 | 4:1064970 | GGTAGCGTGTGCCAG[-/AG]TTTCCTTCCATTTTA | 285498 |
| rs150417048 | in-del | -/AG | 0.0170251 | 0.090679 | intron-variant | RNF212 | GRCh38.p7 | 4:1098732 | CCCTACGTATAAAAC[-/AG]AAGCAGAAACAGCAC | 285498 |
| rs150444411 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1077804 | TGAGGGGGCAGGTGG[C/G]GTCCTCGATGTGGGC | 285498 |
| rs150460737 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF212 | GRCh38.p7 | 4:1064320 | ACCTCAGTGAGTGTT[C/T]ACTGTGGTGAGTTCA | 285498 |
| rs150473607 | in-del | -/ACACACACACACACAC | | | intron-variant | RNF212 | GRCh38.p7 | 4:1106250 | TAAACAATTTTACTT[-/ACACACACACACACAC]ACACACACACACACA | 285498 |
| rs150570527 | in-del | -/AGGACCAACAC | 0.268724 | 0.249298 | intron-variant | RNF212 | GRCh38.p7 | 4:1079000 | ACACAGGACCAACAT[-/AGGACCAACAC]AGGGTCAACACAGGA | 285498 |
| rs150583906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1101563 | CTACTGGGGAAGAAA[A/T]AAGCTAATGAAATAG | 285498 |
| rs150599718 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1063355 | AAAATACTTAAAGCA[A/G]CAAGAGAAGAGCAAC | 285498 |
| rs150642883 | snp | A/G | 0.0153776 | 0.0863269 | intron-variant, missense, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1093984 | CTGGGCATAACTTGA[A/G]ACGGCAACAGCCTCG | 285498 |
| rs150703751 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | RNF212 | GRCh38.p7 | 4:1089443 | ATTAACTTGTTTTTG[A/C]TTCTACAGGCTCATA | 285498 |
| rs150710233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF212 | GRCh38.p7 | 4:1110424 | TTGGGTCAGTTTTCA[C/T]GTGCACATCCGCAGC | 285498 |
| rs150792078 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | RNF212 | GRCh38.p7 | 4:1066562 | TCTCGAACTCCTGAG[C/T]TCAAGCGATCCTTTT | 285498 |
| rs150846610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF212 | GRCh38.p7 | 4:1069595 | GTGACCAAAGTGAAG[A/C]GGAATCAATCAGGTG | 285498 |
| rs150861394 | snp | C/G | 0.021333 | 0.101051 | intron-variant | RNF212 | GRCh38.p7 | 4:1057396 | TCGGTTGACAGAGAC[C/G]TCGGTGTGTGCTTAA | 285498 |
| rs150873976 | in-del | -/A | 0.19646 | 0.2442 | intron-variant | RNF212 | GRCh38.p7 | 4:1064022 | TATGGAAAAAAAAAA[-/A]TGAAGAGAACTGACT | 285498 |
| rs150956544 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF212 | GRCh38.p7 | 4:1106178 | CACTGCGGAAGAAAG[A/G]GCCCACACGGTCTGT | 285498 |
| rs151010222 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF212 | GRCh38.p7 | 4:1091228 | CAGAATGAGGCTAAG[C/T]GAGACCCACAGAGCT | 285498 |
| rs151042310 | snp | C/T | 0.00108672 | 0.0232848 | missense, intron-variant, nc-transcript-variant, downstream-variant-500B | RNF212 | GRCh38.p7 | 4:1073026 | GTGTTTTAGAGTTGG[C/T]GAGTTCCCCGTGCCT | 285498 |
| rs151080487 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF212 | GRCh38.p7 | 4:1081169 | AACACTGGGTCACAT[C/G]ATCATTCCCAAACCA | 285498 |
| rs151164243 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF212 | GRCh38.p7 | 4:1072209 | GGAGAGTCTGAAAAA[C/G]GGACCGTAAAAAGAT | 285498 |
| rs151172066 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF212 | GRCh38.p7 | 4:1059211 | CAGCCTCCGTGCCCC[C/T]GACAGGGGTCTTGTC | 285498 |
| rs151308849 | in-del | -/G | 0.0399052 | 0.1355 | intron-variant | RNF212 | GRCh38.p7 | 4:1087523 | GTGACAGGATGAGGT[-/G]GGGGGGGTGACAGGA | 285498 |