| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs535486359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118003 | TTCAGGCTGTTCTTA[C/G]TAATCTTGACTCTGT | 51444 |
| rs535632333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32107277 | AGGTGCACGCTGCCA[C/T]GCCCAGCTAATTTTT | 51444 |
| rs535716137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105904 | ATCAACAAATGGTAG[C/T]TGAAGCAAAGCACAT | 51444 |
| rs535728131 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32120549 | AAATCATAAGTTTTT[A/T]AAAAAATAATAATTT | 51444 |
| rs535814114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112996 | TGACAGGGCAATGAC[A/G]TGAAGCTGGAAAACA | 51444 |
| rs535864738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119837 | TAAAAATGAGCCCCC[C/T]TTTTTTCCTGTTTGA | 51444 |
| rs535883480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122468 | TACAATTTTTCTTAG[C/T]CACTACTTATCTTAT | 51444 |
| rs535889343 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101426 | AAATTAGAGTCAGGG[A/T]TTCACCATGTTGGCC | 51444 |
| rs536019000 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32109879 | CGACAGAGCGAGGCT[C/G]TGTCTCAAAAAAATA | 51444 |
| rs536040080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117128 | GATGGTCTCGAACTC[C/T]TGACCTCAGGTGATC | 51444 |
| rs536111015 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106055 | TCTCCTTTCCCTTGT[A/G]CATTTTAAATTTATT | 51444 |
| rs536266441 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131542 | TGCTTTATTTTTCAA[G/T]TAAAAGTGGTTTTCT | 51444 |
| rs536302436 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094232 | TTGAGGTGAGGTTCT[A/G]TAATTTTGTAAAGGA | 51444 |
| rs536313874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103702 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 51444 |
| rs536348574 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32104267 | ATCCCCCCACTTCGG[C/T]GTCCCAAAGGGCTGA | 51444 |
| rs536378623 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129985 | GAAACTCTTATTAGA[A/C]ACTTTCAGTTGGTGA | 51444 |
| rs536503146 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121477 | TCCAGCCGGGGCAAT[A/G]AGAGCGAAACTCCAT | 51444 |
| rs536578617 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092135 | CGGCTGCGAAGATAG[C/T]GGCGGCCGGACAGGA | 51444 |
| rs536639932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098175 | GTATTTTTAGTAGAG[A/C]CAGGGTTTTACCATG | 51444 |
| rs536671704 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091847 | ACCGCGGGCGCCCAG[A/C]TGCTTACGTCACAAC | 51444 |
| rs536712920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112872 | CTATAGATTTATCAC[C/T]GACATTTTTTCTAAT | 51444 |
| rs536866767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128170 | GCATAAAATTGATAG[A/C]AAATATAATTTTTTA | 51444 |
| rs536962231 | in-del | -/AAAT | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131241 | GCTTTTTCATAAGGA[-/AAAT]AAATACTTTATTTGC | 51444 |
| rs537069622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094648 | TAGGGCACAATATAG[A/G]TCTTCCACCTTTAAT | 51444 |
| rs537086118 | in-del | -/AAT | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32114124 | TTTTTTTGAGTAAAA[-/AAT]AAGTTGGAGATTTTT | 51444 |
| rs537115069 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32106620 | CACAGGCTTGAGTGC[A/G]GTTGTGCGATCTCGG | 51444 |
| rs537148984 | in-del | -/G | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32112026 | TTTGAAAAGATGAAA[-/G]GTATTTAGACTGGGA | 51444 |
| rs537237733 | snp | A/C | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32096109 | CGTTATTGGCAGGAA[A/C]TTACTGTGTAAGCTA | 51444 |
| rs537508472 | snp | A/C | 0.00127119 | 0.0251789 | intron-variant | RNF138 | GRCh38.p7 | 18:32128885 | CTGTGATGATCCTCT[A/C]TGTTTGTTTGTTATT | 51444 |
| rs537580552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114521 | AACTTCAGGATCTCT[A/G]TGTGAGCTCCTGCCC | 51444 |
| rs537630064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105831 | TTGCTGCAACAGATT[A/G]TATCAGAACAGATAG | 51444 |
| rs537642736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102740 | CAGGTTCAAGTGATT[C/T]TCCTGCCTCAGCCTC | 51444 |
| rs537741888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32109133 | TTGGTATTTCCCACC[A/G]TTTTCATTTTTGTCT | 51444 |
| rs537832289 | in-del | -/A | 0.0414363 | 0.137845 | intron-variant | RNF138 | GRCh38.p7 | 18:32112117 | TGAGAAATGAGACTG[-/A]AAAAAAAATCACTGA | 51444 |
| rs537848253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093562 | CGGGCATTGAAATGA[A/G]CGTTCCCCTTTGTTT | 51444 |
| rs537894595 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105645 | CTTAAACTTTAGAAG[A/G]AAATGTGGGGGAATA | 51444 |
| rs537926549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099580 | GCTAATTTTTTTGTA[C/T]TTTTAGTAGAGATGG | 51444 |
| rs537961328 | snp | C/G | 0.000271592 | 0.01165 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092860 | GGTGCTCAAAACGCC[C/G]GTGCGGACCACGGCC | 51444 |
| rs537980028 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32117292 | CTCTAATTATGCGAT[C/T]TGAGGAGAATTTAGT | 51444 |
| rs538189731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119644 | GGCCAAGCTGGTCTC[A/G]GCCTCCTGGCCTCAG | 51444 |
| rs538238961 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123801 | GGTATTACAGGTGCC[C/T]GCCACCACGCCCGGC | 51444 |
| rs538243078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096459 | TAGATCTGGAATACA[C/T]GGAGCTAAAGCTGTG | 51444 |
| rs538272154 | snp | C/G | 1.65081e-05 | 0.00287293 | intron-variant | RNF138 | GRCh38.p7 | 18:32129101 | TTTTCCTGTTGACAT[C/G]AATGTTATTGTTTTT | 51444 |
| rs538413182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120414 | GATCCTATTGAATGC[A/G]GTAAACCAAGTGTGA | 51444 |
| rs538460367 | in-del | -/GTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105650 | ACTTTAGAAGGAAAT[-/GTG]GGGGAATATCTCTGA | 51444 |
| rs538700336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102225 | TTTTTTTTTTGAGAC[C/G]GAGTCTTGTTCTGTC | 51444 |
| rs538860705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105691 | TGGGGAATTCTTAAG[A/C]CTGCAAAAGCATAAA | 51444 |
| rs538920066 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129853 | AAATTTCTTTCTTTC[A/G]TGGGCATTTGATAAT | 51444 |
| rs538936587 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32104252 | TCCTGAGGTCAAATG[A/T]TCCCCCCACTTCGGC | 51444 |
| rs539010090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103592 | AATCAATAAACAGCA[A/G]TTTTCCACAAAATAT | 51444 |
| rs539109017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119456 | TTGAGACAGAGTCTA[A/T]CTCTGTCTCTCAGGC | 51444 |
| rs539170035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109838 | TTGCAGTGAGCCAAG[A/T]TCGCACCAGTGTACT | 51444 |
| rs539203376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112382 | CTTATGTATTTATGT[A/G]TGTATTTAAGAAATC | 51444 |
| rs539233080 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114382 | TCTCAGATTCATGTA[C/T]ATTAAACATTTTTAT | 51444 |
| rs539350932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098101 | AAGCGATTCTACTCC[C/G]TCAGCCTCCCAAGTA | 51444 |
| rs539379397 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091128 | TCCCACCACCATGTC[C/T]GGTTAATTTTTGTAT | 51444 |
| rs539688216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107086 | TCTTGTGTGTTAACT[C/G]TCTCTGGTTAAATTC | 51444 |
| rs539715514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32100588 | TTAAGCGATTTTCCT[A/G]CCTCAGCCTCCCAAG | 51444 |
| rs539753748 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32093770 | AAATTTTATGGACAG[C/T]TAGGGTGTGAGTAAG | 51444 |
| rs539753827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100977 | AGGTTTCGAGAGAGT[A/T]TAAGAGAGGGATCAG | 51444 |
| rs539860894 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32121095 | AGCCGCGATCGCGCC[A/G]CTGCACTCCAGCCTG | 51444 |
| rs539897617 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117596 | ACACACTCCACGTTA[C/T]GAATATACGGGAATT | 51444 |
| rs539954112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32128074 | GACAGTGCGAGACTC[C/T]GTCTCAAAAAAGAAA | 51444 |
| rs539971773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120698 | AGTAATAGTGGAAAA[C/T]TGAGAGTTATAATGG | 51444 |
| rs540009473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108541 | ATTTTCATTTTGTGA[A/C]TATACCATAATTAGT | 51444 |
| rs540022378 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110476 | TTATTATTTCGTGAG[G/T]GAGGAAACTGATATT | 51444 |
| rs540023177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32097752 | GGTCTCGAACCCCTG[C/T]GCTCAAGTGATCTGC | 51444 |
| rs540095201 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32102986 | TGATTTTTTGCTTTT[C/G]TATATTTTTATGCCT | 51444 |
| rs540182125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32103737 | GGGAGGCCGAGGCGG[A/G]TGGATCACGAGGTCA | 51444 |
| rs540182230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096915 | AAAAAAATTTTTTTG[G/T]AGAGATGGGTCTTGC | 51444 |
| rs540246598 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32109446 | CATTGTTTTATTATT[A/G]CTATTTTTTTAGAGA | 51444 |
| rs540300319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098231 | GGCTGGTTTTGAACT[C/T]CTGACCTCAAGTGAT | 51444 |
| rs540312623 | snp | A/T | 0.00159617 | 0.0282053 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32132004 | CTTAACAGCTGCTAC[A/T]CAAACCCCTTGTAGA | 51444 |
| rs540413495 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091896 | GCCGGTTGCTATACA[G/T]GCCGCACTTCACACC | 51444 |
| rs540556787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118261 | TTTGTTATGGCTGGG[C/T]GCAGTGGCTCACGCC | 51444 |
| rs540593662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126594 | GCTTCTCACGTAGAT[A/G]TTTTTGGTAACATAT | 51444 |
| rs540636776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127832 | ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 51444 |
| rs540737773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094211 | CGACTTTTTTTTCTT[C/T]TTTTTTTGAGGTGAG | 51444 |
| rs540851121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104658 | TTAATAGAAGAAAAA[C/T]GTCACTTACAATAGC | 51444 |
| rs540918123 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108060 | GAGTTTTGCCATGTT[A/G]GCCAGGCTGGTCTTG | 51444 |
| rs540958000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110804 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 51444 |
| rs540964254 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115267 | TTCTTAGATCCACTT[C/G]GTCATAGACACTTGA | 51444 |
| rs540999144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113338 | GCTGGGATTACAAGC[A/G]CGAGCCACTGCACCC | 51444 |
| rs541050271 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095742 | TAACATTACTAAAAT[A/T]TAAACTCCCGTTTAA | 51444 |
| rs541247430 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32107719 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTAG | 51444 |
| rs541493947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108192 | AAATGCATACAGAAA[C/T]GTGTCCCTATCACAG | 51444 |
| rs541585655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101804 | TATTTTAATACAGTT[C/T]ATAGTGGTGTCTAGA | 51444 |
| rs541650790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122162 | GTGAGCCACTGTGCC[C/T]GGCCTGGGTTATGTA | 51444 |
| rs541664300 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121646 | AAAACCCAGTGATTA[A/T]ATTAATTTGGAAGAT | 51444 |
| rs541698715 | in-del | -/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090980 | CTTTTTTTGTTCTTC[-/T]TTTTTTTTTGAGAGT | 51444 |
| rs541803550 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092536 | CCAAGCACCGTCCCC[C/T]ATCCAGCCCCCTGTG | 51444 |
| rs541825427 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32105531 | AGGTGGCTTTGATCA[A/G]TAAGATAGTATTTGG | 51444 |
| rs541879012 | snp | A/C/T | 5.71046e-05 | 0.00534318 | intron-variant | RNF138 | GRCh38.p7 | 18:32111749 | TGTCACAATGTTTGG[A/C/T]TTAGTTTCTGTAGAA | 51444 |
| rs542076466 | in-del | -/AAA | 0.0182019 | 0.0936463 | intron-variant | RNF138 | GRCh38.p7 | 18:32112682 | AGCGAAACGCTGTCT[-/AAA]AAAAAAGAAGAAGAA | 51444 |
| rs542088868 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091932 | CCTCCCCGCCTCTCC[G/T]GGCTCCTCCGCCCAG | 51444 |
| rs542336455 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096762 | TTTGAAATAGGGTCT[C/T]GCTCTGTTGCGAGGA | 51444 |
| rs542351767 | snp | C/T | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091471 | CTTGGTGAAAAGCCA[C/T]GTCCATGCTTCTACG | 51444 |
| rs542410265 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122362 | GTAGATGATATAGTA[C/G]TCCTTGTCTTTTTAT | 51444 |
| rs542467310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108883 | AGCAAAGTCTCACTA[A/T]GTTGTCCAGGCTGGC | 51444 |
| rs542467887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112488 | GTCAGGAGTTCGAGA[C/T]CAGCCTGACCAACAT | 51444 |
| rs542472982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32099424 | TTATTTTATTTTTAG[A/G]CAAAATCTCGCTCTG | 51444 |
| rs542555478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109407 | CAAAGTGCAGGATTA[C/T]AGGTGTGAGCCACTG | 51444 |
| rs542558171 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101573 | AAGAAAAATTTATTT[A/T]TTTTTAAGAATTCAA | 51444 |
| rs542584389 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130641 | AAGGTATATTTTGGT[C/T]TTGTTAAAACCCTTG | 51444 |
| rs542614175 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091351 | TATAGATTATCAATT[G/T]TACAGATAATTGCAC | 51444 |
| rs542623090 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131919 | CAAATACAATGTCAT[A/G]TACCTTGTATGGGTT | 51444 |
| rs542697278 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129335 | AAATAAAGGTAGGGC[C/T]TCTAAAAACTTCATC | 51444 |
| rs542734037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122069 | AGACGGGGTTTCACC[A/G]TGTTGGCTAGGCTGA | 51444 |
| rs542758971 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32097734 | CACTATATTGGCCAG[C/G]CTGGTCTCGAACCCC | 51444 |
| rs542781678 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32129057 | GATGTCTAATGTTTT[A/G]GGCAAAGTATTAGAG | 51444 |
| rs542785426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102864 | TTGAACTCCTGACCT[C/T]AGGTGATCCACCTGC | 51444 |
| rs543005802 | in-del | -/ATAA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123271 | TTAATTTTAAAGAAC[-/ATAA]ATAAGAATCTAGTAA | 51444 |
| rs543075293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096872 | GCTAGCTGGGACTAC[A/C]GGCACTCACCACCAT | 51444 |
| rs543265290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32110215 | CCAGGCTGGTCTTCA[A/G]CTCCTTGCCTCAAGC | 51444 |
| rs543303746 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123398 | GGAAAAAGGTGTATT[G/T]AAGTTCAGACTTTTA | 51444 |
| rs543340397 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32116938 | GACAGAGTTTTGCTC[A/G]TCTCCCAGGCTGGAG | 51444 |
| rs543431609 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32101323 | TCCTAGGTTCAAGCC[A/G]TTCTTCTACCTCAGT | 51444 |
| rs543504400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100663 | TATTTTTAATAGAGA[C/T]GGGGGTTTCACCATG | 51444 |
| rs543544229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093209 | GCGTCTTCAGGCCCC[G/T]GAGGCCCCTGTCGTC | 51444 |
| rs543616576 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32120829 | TGAGTATGTACCCCC[A/G]GTGTTTGTGTTTATT | 51444 |
| rs543659840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112611 | TGTTTGAACCTGGGC[A/G]GCAGAGGTTGCGGTG | 51444 |
| rs543675068 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130055 | ATCTCAGTTTAGAAA[-/T]TTATTCAAAGCTAAA | 51444 |
| rs543723395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094955 | TTTATAATTTGATTT[A/G]ACCTCAAGACTGTGG | 51444 |
| rs543725634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127639 | AATTTAGGTGCGCTT[C/T]ATTGCTTTAGCAATT | 51444 |
| rs543964710 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091914 | CGCACTTCACACCCC[C/G]TGCCTCCCCGCCTCT | 51444 |
| rs543977225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107479 | GCAGTTTTTTTTTAA[A/C]GGCCAGTTAGAAGAT | 51444 |
| rs544058309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101664 | TAAGTGTTAACTGCT[A/G]TTTTCATAAATGTCA | 51444 |
| rs544065591 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32097815 | GGCATGAGCCACTAT[C/T]CTCGGCCTAATTAAT | 51444 |
| rs544090631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116240 | TGCCAGCTGATTGAC[C/T]TTTTTCTTCTCCTTG | 51444 |
| rs544098581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095465 | GCGTGAGGCATGGCA[C/T]CTGACCTGTTTTTTA | 51444 |
| rs544142239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104348 | TCCTCATTAAGGGTG[C/G]CTTCCCTAAAATCTA | 51444 |
| rs544170906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103826 | AAAAAATTAGCCGGG[C/T]GCGGTGGCGGGCACC | 51444 |
| rs544204144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110550 | AACTCAGGTTATGTG[A/G]TCTGTTACTGCACCA | 51444 |
| rs544217208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32118418 | ACACACCTGTAGTCC[C/T]AGCTACTCAGGAGGC | 51444 |
| rs544274798 | snp | C/G | 0.0193772 | 0.0965046 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092417 | GGCGCGAGCCCGCGC[C/G]TGGAGCCCGGTGAGG | 51444 |
| rs544363097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110167 | ATTTTTTTTATTTTT[A/G]ATTTTTGTAGAGACA | 51444 |
| rs544404327 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102025 | GGGACTACAGGCGTG[C/T]ACCACCATGCCTGGC | 51444 |
| rs544409970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125016 | AAGCAAAATGAGATA[C/T]TTAAAATTGCAGTAA | 51444 |
| rs544453305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111304 | TGTGGAACAACATGT[C/T]GATATACATCAGTTT | 51444 |
| rs544459142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118825 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAGA | 51444 |
| rs544477240 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128861 | GCATTATAACACTCA[A/C]ATTTTGTTCTGTGAT | 51444 |
| rs544543086 | snp | A/G/T | 5.5021e-05 | 0.00524481 | intron-variant | RNF138 | GRCh38.p7 | 18:32111712 | ATAGAGATGAAGAGA[A/G/T]TAATTTTTTTTGTAA | 51444 |
| rs544661783 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119342 | GGGGATCAAACAGTC[C/T]TCCCGCCTTGGCCTC | 51444 |
| rs544670384 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093725 | AACGCATGCGTTTGA[C/T]TGGCAGGCATATTTA | 51444 |
| rs544677751 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32095373 | GACAGGGCCTCACTA[C/T]GTTGCCCAGTCAGAT | 51444 |
| rs544848797 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32121877 | ATTTAGGTTATGTAC[-/T]TTTTTTTTCAGACTG | 51444 |
| rs544936947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115423 | TGTTTTACATTCTAT[C/T]GCCAAAGTAATATTA | 51444 |
| rs545013802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108305 | TAGCATCCCAGAAAC[G/T]CCCCTAATGTTCCCT | 51444 |
| rs545245304 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32114639 | GCATGTATCCCTAAA[C/G]AATGCATTGTTAATT | 51444 |
| rs545358163 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094098 | GCCCCGCCCGGAAAT[C/G]TTTATTTTTAAAAAA | 51444 |
| rs545408306 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131784 | TATGAAGTGTCTGCG[C/G]AGCAAGATTTTCAAG | 51444 |
| rs545445074 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32102403 | AGATGGGGTTTCACC[A/G]TGTTAGCTGGGATGG | 51444 |
| rs545638678 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096527 | AAAGATTGAAGAGCA[C/T]CTAGATAGAGCCAAG | 51444 |
| rs545677273 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130463 | AGAATCACAAAGTAT[G/T]TTGTAGAAGGCCCAA | 51444 |
| rs545746371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122653 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 51444 |
| rs545801458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32099801 | TAGGCTGCAAGCTTT[A/G]TAAAGAAAGCATCCA | 51444 |
| rs545932731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106014 | GTTTGGCTATGAGTT[C/T]TCTCTTGGAATACCT | 51444 |
| rs545968847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099398 | AGATAAGAGACCTGA[A/G]TATCTCTATTTTATT | 51444 |
| rs545991371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125999 | CATTTCTGCATAATA[C/T]TCGATATATCATAAA | 51444 |
| rs546017100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32112553 | AGCCAGGTGTGGTGG[C/T]GCATGCCTATAATCC | 51444 |
| rs546028185 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32126436 | TATTAAAAGCTAGAT[A/G]TGGTTTTTCTGTTGA | 51444 |
| rs546030061 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32119233 | TAGGAGGTGATCCAT[G/T]GTTCATTCCTCTAGA | 51444 |
| rs546074866 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32115312 | ATTCCTCATCTGTAC[-/TT]TTATTTTATCTTGTC | 51444 |
| rs546092662 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32093053 | AGAGTCCCGGGGCGG[C/G]CTTTTCCTCAGCCTC | 51444 |
| rs546135846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101282 | TGCAGTGGCACACGC[A/C]GTCTTGGCTCACTGT | 51444 |
| rs546324746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102099 | TGTTACCCAGAATGG[C/T]CTCAAACTCCTGGAC | 51444 |
| rs546355774 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129812 | AGATATTTTCTTTTT[C/G]TTATTAGAAGGAAAT | 51444 |
| rs546413929 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32108976 | CATGGTTTTATGTAT[A/T]TAGGTTTGATGGGTA | 51444 |
| rs546435273 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131200 | TGAGTTAAATATCAT[C/T]GATAGTCTTGTGTGT | 51444 |
| rs546444315 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090453 | GCTGCTAAGGAGGAA[A/C]AGCAACAAAAATACA | 51444 |
| rs546449412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096437 | AGTTAAGTGTGTATA[C/T]CATATGTAGATCTGG | 51444 |
| rs546504471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113187 | TAAGCAATCCTCCTG[C/T]CTCAGCCCCACAGGT | 51444 |
| rs546673961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32108416 | CTAAAAAATAGAATC[A/G]TGCAGTTTGTACTCT | 51444 |
| rs546810168 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103393 | TGGGGAAATCTCACT[A/G]TGTTGCCCAGGCTGG | 51444 |
| rs546944956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116613 | CTGGAGTGCAATGGC[A/G]TGAACATGGCTCACT | 51444 |
| rs546983569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32109746 | ACAAAAATTAGCCGT[C/T]GCAGTGGTGCATGCC | 51444 |
| rs547020734 | snp | C/T | 0.00319098 | 0.0398384 | intron-variant | RNF138 | GRCh38.p7 | 18:32126587 | TAAAAATGCTTCTCA[C/T]GTAGATATTTTTGGT | 51444 |
| rs547090183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112226 | CTGGCATTTAGCTCA[C/T]TTAAACCCCATTCTG | 51444 |
| rs547174848 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129569 | GTAGCAAATTTTGAA[C/T]GATGTGATTGATATA | 51444 |
| rs547238746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32098008 | GTTTGTTTGTTTTGA[A/G]ACAGTCTCACTGTGT | 51444 |
| rs547308758 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102828 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGC | 51444 |
| rs547354121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104133 | ATTCTAGTGACTTAG[C/T]CTCCCAAATAGTTGG | 51444 |
| rs547653186 | in-del | -/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100221 | ATATATATATATATA[-/TA]AAATCTTTGGTTGTA | 51444 |
| rs547664220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112663 | CTCCAAACTGGGCAA[C/T]AAGAGCGAAACGCTG | 51444 |
| rs547815994 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32102944 | CCAATTTGGGATTTT[C/G]TAACAAAATAGTTTT | 51444 |
| rs547846090 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112056 | AATTGGATAGAAAAG[G/T]CCAAAAAAAGCTGTG | 51444 |
| rs547979648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121686 | TGGTTAGAAACATCT[A/G]CCAATTTTAAATGTA | 51444 |
| rs548091050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128482 | GGTGGAGGTTGCAGT[C/G]AGCCAAGATTGTGCC | 51444 |
| rs548093093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121086 | TTTGCAATTAGCCGC[A/G]ATCGCGCCGCTGCAC | 51444 |
| rs548094550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117689 | TCTAAAATAATCTGT[G/T]TCACTTTCATTCATA | 51444 |
| rs548264362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103986 | AAAAAAGAAAACTTC[A/G]TAGCAAATTAGGAAT | 51444 |
| rs548271573 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32111015 | TTGATCTCCTGACCA[C/G]GTGATCCGCCTGCTT | 51444 |
| rs548309664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105137 | CCCTCTGTCCCCCAG[C/G]CTGGAGTGCAGTGGC | 51444 |
| rs548335045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32117154 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGAT | 51444 |
| rs548417637 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125572 | AATAGGAAGGAAAAT[G/T]TTATCAATAAGAACT | 51444 |
| rs548437608 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104660 | AATAGAAGAAAAACG[G/T]CACTTACAATAGCAA | 51444 |
| rs548451339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32123787 | CCTCCCAAGTATCTG[A/G]TATTACAGGTGCCTG | 51444 |
| rs548556032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099517 | AAGAGATTCTCCTGC[C/T]CCAATCTCCCGTGTA | 51444 |
| rs548581231 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125113 | AATGAAAGATGAACC[A/G]GGAACTCATTCCTGC | 51444 |
| rs548584562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098858 | ACTCCGTTTCAAAAA[A/C]AAAAAAAAAAAGATT | 51444 |
| rs548647175 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092718 | GTCGGGCCCCGGGCC[A/G]CCACCGTCACCTCGG | 51444 |
| rs548659230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113933 | GGGAACTATATGATA[A/C]GGTATTTGGGGGGAT | 51444 |
| rs548697883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32114776 | TTATTTTAGTAGCCT[C/T]TCATTTTACATATTG | 51444 |
| rs548698044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107811 | TGTGAGCCACTGTGC[C/T]GGCCTTATTTAATTA | 51444 |
| rs548814939 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32128894 | TCCTCTCTGTTTGTT[A/T]GTTATTCTTGAACAG | 51444 |
| rs548901445 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120315 | ATATATACATCTGGC[C/T]AGAGTTCCAGATATT | 51444 |
| rs549120398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122741 | AGGCAGAAAAATTGC[G/T]CGAACCCAGGAGGCA | 51444 |
| rs549215168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102003 | CACCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA | 51444 |
| rs549271507 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119379 | TGTTGGGATCACAGG[C/T]ATGAGCCTCTGTGGT | 51444 |
| rs549301137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32095858 | ATAGTCCGCTGGAGA[A/G]ACCTATAAATGAGTG | 51444 |
| rs549314602 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123423 | CTTTTAAAACAAATT[A/C]AGACTAGTCTTCTTC | 51444 |
| rs549331667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122285 | GTGCCTTTTCACTGT[A/G]TACACATTGTTGTAT | 51444 |
| rs549366434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115797 | CACACACTTCCTTAT[G/T]CCAAAGCCCTTTCTG | 51444 |
| rs549408537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116349 | TTTATGCTATTAGAT[A/C]TCTAAACTTTATTGT | 51444 |
| rs549475787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125395 | CTTTTTGATAATGAG[A/G]GAGATAGAGCAGAAT | 51444 |
| rs549694906 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32109161 | TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTAAAC | 51444 |
| rs549705189 | in-del | -/TAA | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32104354 | TAAGGGTGGCTTCCC[-/TAA]TAAAATCTATAGCAA | 51444 |
| rs549752724 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126092 | GTTTTTAAGATGTAC[A/T]TCATTTAAACGTAAG | 51444 |
| rs549795144 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099809 | AAGCTTTATAAAGAA[A/G]GCATCCAAGATCTCC | 51444 |
| rs549802201 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113487 | ACTGCTGGTAGTGTC[C/T]TTTCAAGTGTGAAGT | 51444 |
| rs549804486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118694 | ATTAGCTGGGCGTGG[G/T]GGTGCGCGCCTGTAA | 51444 |
| rs549939273 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110419 | TTTTATACTTGTTAT[C/T]TATTTTAATCCTCTG | 51444 |
| rs549960775 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32100462 | GCCACCACCACACCC[A/G]ACTAACTTTTTTTTT | 51444 |
| rs550037984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119313 | CTATGTTTCCCAGGC[A/C]CGTCTCAAACTCTGG | 51444 |
| rs550079167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120455 | TAAATTAAAAAGCAA[A/G]ACATAACTATGGGAA | 51444 |
| rs550113581 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | RNF138 | GRCh38.p7 | 18:32119192 | TACACATCTCTGCAT[A/C]CTGATTTTTTCTGGG | 51444 |
| rs550127825 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32094475 | ATTTTGTGCAACAAA[C/T]GCAGATTCTTAGGGA | 51444 |
| rs550254819 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32106855 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGCTGAAAA | 51444 |
| rs550269950 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121042 | CGGGAGGCTGAGGCA[A/C]GAGAATCACTTGAAC | 51444 |
| rs550290364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100872 | GGCCTCCCAGAGTGC[G/T]GGGATCACAGGCCTG | 51444 |
| rs550301114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096485 | CTGTGGGTGTCGAAG[G/T]GGTCACCGAGTGAGG | 51444 |
| rs550322782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32127957 | TGTTGGCAGGTGCCT[A/G]TAGTCCCAGCTACTC | 51444 |
| rs550336487 | in-del | -/CC | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32105241 | GATTACATGCACCTG[-/CC]CCACCATACATGGCT | 51444 |
| rs550355210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109473 | GAGACAGGGTCATGC[C/T]GTGTTACCCAGGCGG | 51444 |
| rs550359647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121031 | ACCCAGCTACTCGGG[A/G]GGCTGAGGCACGAGA | 51444 |
| rs550378502 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32127274 | GTTACAAAGAGACTA[-/AG]AGTGTAAGAGAAGTT | 51444 |
| rs550443220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103224 | AATTTAACTCTGTTG[A/C]CCAGGCTGGAGTACA | 51444 |
| rs550504145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123715 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 51444 |
| rs550579387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110931 | AACTACAGGCGCCTG[A/T]CACCACGCCCGGCTA | 51444 |
| rs550603321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102669 | AAATAGTCTCCTTCC[A/G]TTGCCCAGGCTGGAG | 51444 |
| rs550653194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117068 | CACCACGCCCAACTA[A/T]TTTTTGTATTTTTTG | 51444 |
| rs550692696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117565 | ATACTGTTTATTATA[C/T]GTTCTGAAGTGCTGG | 51444 |
| rs550726563 | in-del | -/GGCGCTCCCGCGTTCGGTGACGGCCGGGTAGGCT | 0.0126979 | 0.078662 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091954 | TCCGCCCAGATCCCC[lengthTooLong]GTAGGCAGCGCAATG | 51444 |
| rs550761185 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104116 | CCTTCTGGGTTCAAG[C/G]AATTCTAGTGACTTA | 51444 |
| rs550829938 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131432 | GAGGGAATTGTATTG[A/G]TACTCCAATACCTAA | 51444 |
| rs550836831 | in-del | -/AAAAG | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130569 | TAACTAGAAGAACAT[-/AAAAG]AAAGAGAATCTCAGA | 51444 |
| rs550977798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113578 | AATGAACAGAAATGT[A/G]TTATCTATTCTTAAC | 51444 |
| rs551053785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120296 | CATGTATGAAATTAA[A/G]AACATATATACATCT | 51444 |
| rs551090617 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120981 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGC | 51444 |
| rs551102396 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32107151 | TTGGAGACGGAATCT[C/T]GCTCTGTCACCCAGG | 51444 |
| rs551157952 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116964 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTA | 51444 |
| rs551263708 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101980 | CTCCTAGGCTTAAGC[A/G]ATCCTCCCACCTCAG | 51444 |
| rs551293511 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114385 | CAGATTCATGTACAT[G/T]AAACATTTTTATGAA | 51444 |
| rs551480491 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095229 | GGGTGGAGTGCAGTG[A/G]TGTGATCATGTTTCA | 51444 |
| rs551490368 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129457 | GTTGTACTTTATCTT[C/T]TTGTAATATTATTTT | 51444 |
| rs551559183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128140 | AGGCCTTGATTTTAA[A/C]GCGAAATGCATAGGG | 51444 |
| rs551604513 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107764 | CCTTGTTATCCACCC[G/T]CCTCAGCCTCCCAAA | 51444 |
| rs551655065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100988 | GAGTATAAGAGAGGG[A/T]TCAGATCTAGTGGGT | 51444 |
| rs551714071 | in-del | -/T/TTTTTTTT | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32102043 | ACCATGCCTGGCTGA[-/T/TTTTTTTT]TTTTTTTTTTTTTTT | 51444 |
| rs551800186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121740 | ATTGGTGACACATGC[A/T]GTTTTTGGTAACAAA | 51444 |
| rs551861645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095750 | CTAAAATATAAACTC[C/G]CGTTTAATCCCCATT | 51444 |
| rs551937682 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123144 | GTAAAAAAGTTCACA[A/G]ATTCTTGAGTCTACC | 51444 |
| rs551965312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108993 | AGGTTTGATGGGTAT[A/G]TACTTCAGAGTGGAA | 51444 |
| rs552101838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111456 | TTTTCCTTTGTACCA[G/T]GCTTCCTCTAGTAAT | 51444 |
| rs552128671 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092789 | GCCATGGCCGAGGAC[C/T]TCTCTGCGGCCACGT | 51444 |
| rs552145820 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107171 | TGTCACCCAGGCTGG[A/C]GTGCAGTGGCGCGAT | 51444 |
| rs552177777 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32100264 | ACAGTAAAATTGGAC[A/G]TAAGAGACCTGAATA | 51444 |
| rs552205496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32124586 | ATGCATCATTTCCTG[A/G]ATACATATGTTCAAA | 51444 |
| rs552262687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098619 | GCACTTTGGGAGGCC[C/G]AGGCAGGCGGATCAC | 51444 |
| rs552320890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126213 | CCAGCCTGGACAACA[A/G]TGAGACTGTGTCTCT | 51444 |
| rs552340979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105800 | CAAATGATGGACTGA[A/C]TGTCGTCTGTTCTAC | 51444 |
| rs552361617 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121296 | AGGTTGGGAGTTTGA[C/G]ACCAGCCTGACCAAC | 51444 |
| rs552471292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111060 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 51444 |
| rs552492038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117757 | TATTGGAGGATGTTT[C/T]AGCAAAATTATTGCA | 51444 |
| rs552501194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094339 | TCCCCAATCTTAACT[A/G]CACTGTCTACTTTAT | 51444 |
| rs552561955 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109380 | TTAAGCCATTTGCCC[C/T]GCTCAGCCTCTCAAA | 51444 |
| rs552649263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101523 | TTATTTTTTTAAGCC[C/T]TAGTTTCCTCATCTG | 51444 |
| rs552716515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121993 | CATGCCTCAGCCTCC[C/T]GAGTAGTTGGGATTA | 51444 |
| rs552784301 | in-del | -/TTTTT | 0.00398564 | 0.0444627 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090981 | CTTTTTTTGTTCTTC[-/TTTTT]TTTTGAGAGTCTCAC | 51444 |
| rs552792475 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32094788 | CTGCTAACTATATAT[A/G]TATATATAAAGCAGG | 51444 |
| rs552828207 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121301 | GGGAGTTTGAGACCA[C/G]CCTGACCAACATGGA | 51444 |
| rs553069312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095346 | GACTAATTTTGTTTT[A/C]TTTTTTATAGAGACA | 51444 |
| rs553217924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109251 | CTCTGCCTCACAGGC[C/T]CAAGTGATCCTCTCA | 51444 |
| rs553315995 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091012 | TCACTCTGTCGCCAG[A/G]GCTGGAGTGCAGCGG | 51444 |
| rs553421211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108819 | GACTACAGGCATGCA[C/T]CACCGTGCCCAGCTA | 51444 |
| rs553530387 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32102362 | GCCCGCCGCCACGCC[C/T]GGCTAATTTTTTGTA | 51444 |
| rs553571853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111159 | CCTACTTCCGGACCA[A/C]ATAACCAAATATCTG | 51444 |
| rs553601167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32123694 | TCTCACTTTGTTTTC[C/T]CAGGCTGGAGTGCAG | 51444 |
| rs553641517 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090218 | TCCACTGCACCCCAG[C/G]CTGGGTGACAGAGTG | 51444 |
| rs553671808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095912 | TGTGAGCATCTAGAG[C/G]AGGTATCTAAATTAG | 51444 |
| rs553702711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111603 | TCTGATAAATACATA[C/T]ACAGTTACTAAACTT | 51444 |
| rs553703025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096740 | TTTTGTTTTTGTTTT[C/T]GTTTTTTTTGAAATA | 51444 |
| rs553739994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32097559 | TGGGATCTTGGTTTA[C/T]TGTAACCTCCACCTC | 51444 |
| rs553772419 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32108134 | TGCTGGGATTACAGG[A/C/T]GTAAGCCACCATGCC | 51444 |
| rs553774776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105533 | GTGGCTTTGATCAGT[A/C]AGATAGTATTTGGGC | 51444 |
| rs553816262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32092904 | GAGTAGACGCCCCCT[A/C]CCCCTCGCGGAGCCG | 51444 |
| rs553824288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107633 | TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCCAAG | 51444 |
| rs553920465 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32107284 | CGCTGCCACGCCCAG[A/C]TAATTTTTTTTTGTA | 51444 |
| rs553925488 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112519 | GGTGAAACCCCGTCT[C/G]TACTAAAAATAAAAA | 51444 |
| rs553957499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101163 | GGAACATGCAGGGCT[C/T]TGTATTTGAATGACA | 51444 |
| rs554081411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107917 | GCCCAGATTGGGGCG[C/T]GATCTCGGCTCACTG | 51444 |
| rs554199058 | in-del | -/AAA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118840 | GTCTCAAAAAAAAAG[-/AAA]ATAATAATAATAATA | 51444 |
| rs554282697 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117418 | AAGCAGGAGAGAGGA[A/G]GAAATAGATAACAGA | 51444 |
| rs554286331 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099072 | CAGTGTTGTTGATTA[C/G]CCTTTTGTTGGGAGA | 51444 |
| rs554287362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32126372 | TGAGATAATATATTG[A/G]ATATGTTGCAGGCAG | 51444 |
| rs554353842 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103722 | TAATCCCAGCACTTT[G/T]GGAGGCCGAGGCGGG | 51444 |
| rs554431801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113028 | ACTCGAGAGATTCTG[A/G]CTATTCCTCTCAGTG | 51444 |
| rs554507536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122514 | TCTACTATTGAAAGA[C/T]GTTGCTTTTATAAAA | 51444 |
| rs554563007 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131627 | ATTCACACTGAAAGA[C/T]GTAGGAGATAACCCA | 51444 |
| rs554574354 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123966 | CATAAATTAAACTTA[-/A]AAAAAAAAAAAAAAA | 51444 |
| rs554694145 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091849 | CGCGGGCGCCCAGCT[A/G]CTTACGTCACAACCC | 51444 |
| rs554701391 | snp | A/G | 0.000165003 | 0.00908153 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124796 | ATTTTACCAGACAGC[A/G]TTTACTGGATCACTG | 51444 |
| rs554723653 | in-del | -/AGAT | 0.00716266 | 0.059414 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131853 | AACACTTTTATATGG[-/AGAT]AGATAGATAGTACTT | 51444 |
| rs554725032 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130076 | CAAAGCTAAAGATGT[A/G]TATATACATATACTT | 51444 |
| rs555040146 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32107232 | TTTAAGCAGTTCTCC[C/T]GCCTCAGCCTCCTGA | 51444 |
| rs555045380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097742 | TGGCCAGGCTGGTCT[C/T]GAACCCCTGCGCTCA | 51444 |
| rs555360864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094653 | CACAATATAGATCTT[C/T]CACCTTTAATCTAGC | 51444 |
| rs555566132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121944 | CATGATCTTAGCTCA[C/G]TGCAACCTCCGCCTT | 51444 |
| rs555764485 | in-del | -/AAACCCCTTAACAGCTGCTACTC | 0.00199481 | 0.0315187 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131983 | TCATAACTTCTACAG[-/AAACCCCTTAACAGCTGCTACTC]AAACCCCTTGTAGAA | 51444 |
| rs555805762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32108655 | ATTTTTTCTGATTAT[A/G]TATGTAATTTTTGTT | 51444 |
| rs555860974 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095451 | TGCTGGGATGACAGG[C/T]GTGAGGCATGGCACC | 51444 |
| rs555972254 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111116 | ATTTCTCAAATTATG[C/T]TCCATTGCATACTGT | 51444 |
| rs555972821 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092427 | CGCGCCTGGAGCCCG[G/T]TGAGGGCGTGGCCTA | 51444 |
| rs556021771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32102350 | GGGACTACAGGCGCC[C/T]GCCGCCACGCCCGGC | 51444 |
| rs556049640 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093678 | GAGATGCTACCCAGG[A/G]TGGGGGAGAACACAA | 51444 |
| rs556058908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32096138 | TAATTTGAGTGTTTT[C/T]CTGAAAACCTATTAA | 51444 |
| rs556063119 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121371 | GTGGTGGTACATGCC[A/G]GTAATCCTAGCTTCT | 51444 |
| rs556071850 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118417 | CACACACCTGTAGTC[C/T]CAGCTACTCAGGAGG | 51444 |
| rs556198496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111085 | GTGCCCGGCAAAGCC[A/G]GAAGTATTCTTAAGT | 51444 |
| rs556201847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124679 | CAAAAAATAGGAGAG[C/T]GTTATTTTTGTGTTA | 51444 |
| rs556215331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099088 | CCTTTTGTTGGGAGA[A/G]TGCGTAATGGAAATT | 51444 |
| rs556246041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32125801 | AAAGAATATGCTTCA[A/G]TAACCATTGAGGATG | 51444 |
| rs556267227 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107278 | GGTGCACGCTGCCAC[A/G]CCCAGCTAATTTTTT | 51444 |
| rs556277677 | snp | C/T | 0 | 0 | intron-variant | RNF138 | GRCh38.p7 | 18:32117293 | TCTAATTATGCGATT[C/T]GAGGAGAATTTAGTA | 51444 |
| rs556297149 | in-del | -/TTTA | 0.245274 | 0.249955 | intron-variant | RNF138 | GRCh38.p7 | 18:32106552 | TTTTATTTTATTTTA[-/TTTA]TTTATTTATTTATTT | 51444 |
| rs556331747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118836 | CTCCGTCTCAAAAAA[A/G]AAGAAAATAATAATA | 51444 |
| rs556348515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32112902 | TAGCTAATGAATTCA[G/T]TGAGCAAAGCTGGTT | 51444 |
| rs556511736 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32089999 | GCCTGTAATTCCAGC[A/C]CTTTGGGAGGCCAAG | 51444 |
| rs556512061 | in-del | -/GA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103874 | GGGAGGCTGAGGCAG[-/GA]GATGGTGTGAACCCT | 51444 |
| rs556550700 | snp | A/C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096600 | AGCCAGACAAGGAAC[A/C/G]AACAGAAGGATAGGA | 51444 |
| rs556684591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32123985 | AAAAAAAAAAAATCA[A/G]TTACATCATTAGGCA | 51444 |
| rs556704722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116078 | TGATGATGATAGGTC[C/T]TCATTGAGTTGAAGT | 51444 |
| rs556722598 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129855 | ATTTCTTTCTTTCAT[A/G]GGCATTTGATAATTT | 51444 |
| rs556731099 | in-del | -/A | 0.141596 | 0.225274 | intron-variant | RNF138 | GRCh38.p7 | 18:32098853 | GTGAGACTCCGTTTC[-/A]AAAAAAAAAAAAAAA | 51444 |
| rs556741436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32109365 | GCTGGTCTTGTGAGC[C/T]TAAGCCATTTGCCCC | 51444 |
| rs556801623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32119804 | TTTTCTAGTAAAACC[C/T]TATAGTTTTTGTTGC | 51444 |
| rs556909732 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32102853 | CAGGCTGGTCTTGAA[-/C]CTCCTGACCTTAGGT | 51444 |
| rs557027919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32109840 | GCAGTGAGCCAAGAT[C/T]GCACCAGTGTACTCC | 51444 |
| rs557202518 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32103637 | TTTATCATTAAAAAA[A/T]TTTTTTTAGACAAGA | 51444 |
| rs557203724 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098684 | AGTGAAACCCTGTCT[C/G]TACTAAAAATACAAA | 51444 |
| rs557421504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102856 | GGCTGGTCTTGAACT[A/C]CTGACCTTAGGTGAT | 51444 |
| rs557440429 | in-del | -/GCCCGGGACCCCGGGCTGCC | 0.0287284 | 0.116357 | intron-variant | RNF138 | GRCh38.p7 | 18:32092945 | TAGGCCCGGCCTCCG[-/GCCCGGGACCCCGGGCTGCC]GCCTGGCGGGAACCG | 51444 |
| rs557802094 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32100601 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAA | 51444 |
| rs557821523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32112395 | GTATGTATTTAAGAA[A/G]TCACAAGGGCCGGGC | 51444 |
| rs557943586 | in-del | -/C | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090178 | TCAACCTGGAAGGCG[-/C]CAGGTTGAAGTGAGC | 51444 |
| rs558083331 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF138 | GRCh38.p7 | 18:32102226 | TTTTTTTTTGAGACG[A/G]AGTCTTGTTCTGTCA | 51444 |
| rs558147652 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32121125 | GGGAGACAAGAGTGA[G/T]ACTGTCTCAAAAAAA | 51444 |
| rs558188885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114505 | AAAGAACATTTTTCA[A/G]AACTTCAGGATCTCT | 51444 |
| rs558197824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108576 | CATTCTTCTGTTGGC[A/G]GACCTATGTATAGTT | 51444 |
| rs558253941 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120997 | AAAAATTAGCCAGGC[A/C]TGGTGGCATGGCCGA | 51444 |
| rs558344445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32098267 | TGCCTTGGCCTCCCA[A/G]AGTGCTAGGATTACA | 51444 |
| rs558394778 | in-del | -/AG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117620 | GGGAATTGGTAAAAC[-/AG]ACATTATTTTTTCCA | 51444 |
| rs558419954 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32107953 | TCCACCTCCCAGGTA[C/T]GAGTGATTCTCCTGC | 51444 |
| rs558440569 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF138 | GRCh38.p7 | 18:32125630 | GTATGCTAGGAAAAG[C/T]TGTGAAAGAATGTGC | 51444 |
| rs558524359 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF138 | GRCh38.p7 | 18:32110120 | CCTCCTGAGTAGCTG[A/G]GACTGGACGTGCATG | 51444 |
| rs558551932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116877 | GGTGTGAGCCACCAC[A/G]CCTGGCCAGAAATGT | 51444 |
| rs558556116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123824 | CGCCCGGCTAATTTT[C/T]GTATTTTTAGTAGAA | 51444 |
| rs558578801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099027 | CTGAAATTGGGAGCA[C/T]GATGAGTGGGAATAT | 51444 |
| rs558587950 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117285 | CAGTGGGCTCTAATT[A/T]TGCGATTTGAGGAGA | 51444 |
| rs558624763 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091899 | GGTTGCTATACAGGC[A/C]GCACTTCACACCCCG | 51444 |
| rs558638746 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092288 | GTGCCGGGAAGCGGG[A/G]CGGGGAGGAAGCCGC | 51444 |
| rs558695385 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32106716 | ACTACAGGCGCCCGT[C/T]ACCATGCCTAGCTAA | 51444 |
| rs558794275 | in-del | -/CT | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131604 | GAGGCAAACATTTAA[-/CT]CTCATAATTCACACT | 51444 |
| rs558800881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118311 | GGCCAAGGTGGGCAG[A/G]TCACCTGAAGTCAGG | 51444 |
| rs558879111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120259 | AAGGTTTCCCCATTA[A/G]TAGTTTTACTCAAAT | 51444 |
| rs558879206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127833 | CACCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 51444 |
| rs559040117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126630 | TGTTATTTTAATACT[A/G]TCAATTGTATAATAT | 51444 |
| rs559165880 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32116820 | GAACTCCTGACCTCC[A/G]GTGATCCACCTGCCT | 51444 |
| rs559233080 | in-del | -/GT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097976 | TGTGTGTGTGTGTGT[-/GT]TATTTTTGTTTGTTT | 51444 |
| rs559246739 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114663 | GTTAATTTTGAAAAC[G/T]TCAGTAGTAAGCACA | 51444 |
| rs559285559 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108201 | CAGAAACGTGTCCCT[A/C]TCACAGATATCCAGC | 51444 |
| rs559461348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107738 | TGGCCAGGCTAGTCT[C/T]GAACTCCTGACCTTG | 51444 |
| rs559574674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113376 | AACTTAATTTTTTTT[A/T]AAGTGCTTTCTAACT | 51444 |
| rs559590571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101405 | TGTGTATATATATAT[A/T]TTTTTAAATTAGAGT | 51444 |
| rs559912096 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF138 | GRCh38.p7 | 18:32095747 | TTACTAAAATATAAA[C/T]TCCCGTTTAATCCCC | 51444 |
| rs559934431 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118801 | GCCACTAACACTCCA[A/G]CCTGGGCGACAGAGC | 51444 |
| rs559938181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122209 | TGCTTGCTCGCTTGG[A/G]CTATGTGTGGAGAGA | 51444 |
| rs560057543 | in-del | -/TAAC | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130684 | ACTGAACATTTTTTT[-/TAAC]TAACTTGATTTAATA | 51444 |
| rs560103248 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129425 | TTTCACTAATGTAAC[A/G]GTGAAAGAGAATCCC | 51444 |
| rs560346766 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092546 | TCCCCCATCCAGCCC[C/G]CTGTGGGAGGAGCCG | 51444 |
| rs560360545 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32111401 | TTAATTTGTTGGCCT[A/G]AGATTACACAGCTAC | 51444 |
| rs560526822 | in-del | -/TTTATTTG | 0.000798881 | 0.01997 | intron-variant | RNF138 | GRCh38.p7 | 18:32106572 | TTATTTATTTATTTA[-/TTTATTTG]TTTGTTTATTGAGAT | 51444 |
| rs560628430 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096794 | TGCAGTGGCATGATC[A/G]TAGCTTACTGCAGCC | 51444 |
| rs560647575 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32093479 | TTTGTTTCGTTTCCA[C/G/T]TCCACTATGTGTTAG | 51444 |
| rs560722340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32102899 | GCCTCACAAAGTGTA[A/G]GGATTACAGGTGTGA | 51444 |
| rs560749035 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094266 | ATTGAATTTTTGGTT[C/G]TTAATTGCAAATGCC | 51444 |
| rs560837090 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF138 | GRCh38.p7 | 18:32109417 | GATTACAGGTGTGAG[C/T]CACTGTGCCTGGCCA | 51444 |
| rs560935780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096905 | CTGGCTATTAAAAAA[A/T]ATTTTTTTGTAGAGA | 51444 |
| rs560941745 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131926 | AATGTCATATACCTT[A/G]TATGGGTTGCTTGGT | 51444 |
| rs560943852 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124309 | AGAGATACGATATTG[A/T]TGGAAGTCTTTTAGA | 51444 |
| rs561063964 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130761 | CAAACAGTAAAGACT[G/T]TATTTATGGATTGTA | 51444 |
| rs561109273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096268 | GCAGGGTTTTCAGCT[C/T]GGTAGTGGTGAGACT | 51444 |
| rs561159260 | snp | A/G/T | 0.000319328 | 0.0126319 | intron-variant | RNF138 | GRCh38.p7 | 18:32123488 | TTTCATTACTTTGAG[A/G/T]TATTAACTTTTTCCC | 51444 |
| rs561361027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32116172 | TTCCTCATCATCCTC[A/G]TTATCACTCCCTCAC | 51444 |
| rs561426277 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129314 | GTCATTTTAGTTTTT[G/T]ATTGAAAATAAAGGT | 51444 |
| rs561492936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117424 | GAGAGAGGAGGAAAT[A/C]GATAACAGAACCTGA | 51444 |
| rs561513184 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32107228 | CGGGTTTAAGCAGTT[-/CTC]CTGCCTCAGCCTCCT | 51444 |
| rs561521234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126102 | TGTACTTCATTTAAA[C/T]GTAAGGATATGGCTG | 51444 |
| rs561575666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110692 | CTGGTTCTCTTGAAA[A/G]CAAAATGATCAAATA | 51444 |
| rs561680932 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116359 | TAGATCTCTAAACTT[C/T]ATTGTATTTATTTAT | 51444 |
| rs561816517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093215 | TCAGGCCCCGGAGGC[C/T]CCTGTCGTCTCCGCC | 51444 |
| rs561912566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106974 | CATATTTTTTAGCTC[C/T]GGAAATTCCCCTCAC | 51444 |
| rs561946568 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101745 | AAAAGTATATTTGTA[A/T]TCCATCATCTTTGCC | 51444 |
| rs562084744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101378 | CGTGCACCACCACTC[C/T]TGGCTAATTTTTGTG | 51444 |
| rs562146292 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115557 | CAAGACCAGCCTGGC[C/T]ATCATGGTGAAACCT | 51444 |
| rs562302878 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129414 | TAAAAAAGATGTTTC[A/C]CTAATGTAACGGTGA | 51444 |
| rs562340131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121593 | TAGTTCTATAAACCT[A/G]TTAGAAGTTGTTAAC | 51444 |
| rs562577940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32124390 | TATTAAAAATTTTCA[A/G]GGGACATACAGTGAC | 51444 |
| rs562584630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103278 | ACTGTAGCTTTGAAC[A/T]CCTGGAGTTAAGGAA | 51444 |
| rs562617304 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32108725 | TCAGGTAGAAGGGTA[A/G]TGGAGTGATCATAGC | 51444 |
| rs562649278 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128507 | TGTGCCACTGCACTC[C/T]AGCCTGAGTGACAGA | 51444 |
| rs562661902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117566 | TACTGTTTATTATAC[A/G]TTCTGAAGTGCTGGA | 51444 |
| rs562711245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106184 | GTTCGTATTTTTATT[G/T]GGATTGTTTGGGTTT | 51444 |
| rs562748675 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099652 | CCAAATGATCTGCCC[C/T]GCCTCGGCCTCCCAA | 51444 |
| rs562752866 | snp | A/G | 0.0182019 | 0.0936463 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091891 | CGTGCGCCGGTTGCT[A/G]TACAGGCCGCACTTC | 51444 |
| rs562756059 | snp | A/G | 0.00119784 | 0.0244435 | intron-variant | RNF138 | GRCh38.p7 | 18:32106572 | TTTATTTATTTATTT[A/G]TTTGTTTATTGAGAT | 51444 |
| rs562795529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098334 | GTTTAAATTTTTTAG[A/G]GATGGGGTCTTGCTT | 51444 |
| rs562809472 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102353 | ACTACAGGCGCCCGC[C/T]GCCACGCCCGGCTAA | 51444 |
| rs562824881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105677 | CTCTGATCCTGAAGT[G/T]GGGAATTCTTAAGAC | 51444 |
| rs562862958 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32118515 | TTCCAGCCTGGGAGA[A/C]AGAGCAAGACTCTTT | 51444 |
| rs562913228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099435 | TTAGACAAAATCTCG[C/T]TCTGTTGCCCAGACT | 51444 |
| rs562990789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32114721 | GCCACTATTATAGAA[A/G]GGTTCCCAGGAGACA | 51444 |
| rs563023114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125061 | AGGGAGATGCATAGT[G/T]TGAGGTAATATAGCA | 51444 |
| rs563067145 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121024 | CCGATAGACCCAGCT[A/C/G]CTCGGGAGGCTGAGG | 51444 |
| rs563158006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119467 | TCTAACTCTGTCTCT[C/T]AGGCTGGAGTGCAAT | 51444 |
| rs563262108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128399 | AAAAATTAGCTGGGT[A/G]TGGTGGTACGTATCT | 51444 |
| rs563305975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108872 | TTTTTTACAGGAGCA[A/G]AGTCTCACTATGTTG | 51444 |
| rs563342857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102405 | ATGGGGTTTCACCAT[A/G]TTAGCTGGGATGGTC | 51444 |
| rs563447210 | in-del | -/AAA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094013 | GCAAGGATGGTCTCG[-/AAA]ATCTCCTGACCTCGT | 51444 |
| rs563467899 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101982 | CCTAGGCTTAAGCGA[C/T]CCTCCCACCTCAGCC | 51444 |
| rs563582021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108346 | AACATATCCCACCTC[C/G]TTCAGGATACCATTA | 51444 |
| rs563830598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116312 | TGAGCTCTAGAATTT[A/C]TTCTTCTTGGTAGAA | 51444 |
| rs563850846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122657 | GGCGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 51444 |
| rs563867255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123233 | TCTGCAAAATTCTCT[A/G]TACTTCTGTAACTGT | 51444 |
| rs563896162 | in-del | -/CTCCCGCT | 0.0652144 | 0.168387 | intron-variant | RNF138 | GRCh38.p7 | 18:32093105 | CCCCCTCAGCCCAAG[-/CTCCCGCT]CTCCCGCTCTCCCGC | 51444 |
| rs563960666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125294 | GTATGTGAATGCATA[A/G]AGCAAGGAAGGAAAA | 51444 |
| rs564198471 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092618 | TCTCTGCGTTCGGCC[C/T]CGCCCTACCCAGGGC | 51444 |
| rs564286842 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32112898 | CTAATAGCTAATGAA[-/T]TCAGTGAGCAAAGCT | 51444 |
| rs564313032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120062 | TTCTATATAATACTT[C/G]ATTTATTGCATTGAA | 51444 |
| rs564403075 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32106256 | CAACCATTTTTTTCC[A/G]TAAGCCCTATAAGTT | 51444 |
| rs564468533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094909 | TAGATTGCTCTAGTC[C/T]GCTTCCCTTGTGGGA | 51444 |
| rs564541125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103067 | GTATATTTTTGAATC[C/T]AGACCATTGCATTTA | 51444 |
| rs564551597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112593 | GGGAGGCTGAGGCAG[A/T]ATTGTTTGAACCTGG | 51444 |
| rs564689688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109449 | TGTTTTATTATTACT[A/G]TTTTTTTAGAGACAG | 51444 |
| rs564736664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127896 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 51444 |
| rs564803346 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32116210 | CTTTTACCAGTAATA[G/T]CCCAACCTGCATTTT | 51444 |
| rs564862136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097778 | TCTGCCCGCCTTGGC[C/T]TCCGAAAGTGCTGGG | 51444 |
| rs564890582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117042 | GAGTAGCTGGGATTA[C/T]AGGTGCCCACCACCA | 51444 |
| rs564959625 | snp | C/G | 0.00159617 | 0.0282053 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32132005 | TTAACAGCTGCTACT[C/G]AAACCCCTTGTAGAA | 51444 |
| rs564980917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117454 | AAGAAGAGAGCTGAA[C/T]AGAGCATGGCTATGG | 51444 |
| rs565027071 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF138 | GRCh38.p7 | 18:32114792 | TCATTTTACATATTG[C/G]TAATTTTTAGTAACT | 51444 |
| rs565175690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32103823 | AAAAAAAAATTAGCC[A/G]GGCGCGGTGGCGGGC | 51444 |
| rs565195457 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32094851 | TTGGGTCATTGACCT[A/G]ATGGGCCTCATTGTA | 51444 |
| rs565261797 | in-del | -/GAC | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130511 | AAGAGTGGATTTGCT[-/GAC]GACATTCCATACTAA | 51444 |
| rs565420861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110840 | GGCTGGAGTGCAGTG[A/G]TGCAATCTCGGCTCA | 51444 |
| rs565480230 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105592 | TGTGCTATACATGAT[A/C]ATATTTCCAGATGGA | 51444 |
| rs565482911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098627 | GGAGGCCGAGGCAGG[C/T]GGATCACAAGGTCAG | 51444 |
| rs565591389 | in-del | -/CTCCCGCT | 0.330714 | 0.236612 | intron-variant | RNF138 | GRCh38.p7 | 18:32093106 | CCCCCTCAGCCCAAG[-/CTCCCGCT]CTCCCGCTCTCCCGC | 51444 |
| rs565780179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119446 | TTTTATTTTTTTGAG[A/G]CAGAGTCTAACTCTG | 51444 |
| rs565812417 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32107069 | GGCCACTGGATTAGG[G/T]CTCTTGTGTGTTAAC | 51444 |
| rs565869691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094565 | TGTGAGATATGCCAT[C/T]CTCAAACCTTGTTAC | 51444 |
| rs565887811 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114378 | CTTATCTCAGATTCA[C/T]GTACATTAAACATTT | 51444 |
| rs565923732 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32122855 | ACTAAATAAATAAAA[C/T]TGACCACATTGATCA | 51444 |
| rs566034965 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF138 | GRCh38.p7 | 18:32106808 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 51444 |
| rs566069141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128026 | CAGAGCTTGCAGTGC[C/G]TGAAGATCACGCCAC | 51444 |
| rs566181284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32127322 | AATTCATAAAGCAAA[A/G]TGGATTAATTTGTAC | 51444 |
| rs566186202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108430 | CGTGCAGTTTGTACT[C/G]TTTTATATCTGGCTT | 51444 |
| rs566276514 | in-del | -/TTTG | 0.0130921 | 0.0798413 | intron-variant | RNF138 | GRCh38.p7 | 18:32107510 | ATCTTAATTTAGTTT[-/TTTG]TTTGTTTGTTTGTTT | 51444 |
| rs566364101 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104768 | AAGTGTAAGAGAACA[G/T]GACATTTATGGTTAG | 51444 |
| rs566407249 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090960 | ATCCCATCTTATCGA[C/T]TTATCCTTTTTTTGT | 51444 |
| rs566494057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098953 | TTGGGGAATGATCTC[A/G]ATTATCGACTCGGAA | 51444 |
| rs566494175 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32105719 | AAACCATAATTTTAG[C/G]AAAAGGCCATGTCTA | 51444 |
| rs566496064 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129612 | TGAGCCAGTTATTAT[A/T]AGAGTTGCAGAATAG | 51444 |
| rs566498741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110459 | ATCAGTTGTAGATAC[G/T]TTTATTATTTCGTGA | 51444 |
| rs566504438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123793 | AAGTATCTGGTATTA[C/T]AGGTGCCTGCCACCA | 51444 |
| rs566527444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099527 | CCTGCCCCAATCTCC[C/T]GTGTAGCTGGAACTA | 51444 |
| rs566558246 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131338 | TGGGAATAGGGATAG[A/G]CTTTACAGATTTATG | 51444 |
| rs566572941 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131666 | CACTTAAAAAAGTGG[A/G]TAAGAAAAAGCTACC | 51444 |
| rs566604074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105238 | CTGGGATTACATGCA[C/T]CTGCCACCATACATG | 51444 |
| rs566881961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32108403 | CTTTTTGTACATTCT[A/G]AAAAATAGAATCGTG | 51444 |
| rs566883879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101493 | CTGCCTCACTCTTAC[A/G]GGTTTATTAACATTT | 51444 |
| rs566979327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118754 | GAATTCCTTGAACCC[A/G]GGAGGCCAAGGTTGC | 51444 |
| rs567044906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107858 | AATATAACTACCCTT[A/G]TTTAAAGGGTACTTT | 51444 |
| rs567057495 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114036 | AATCTGTTTGGCACA[C/T]GTAAGCTCTCATCTG | 51444 |
| rs567137489 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106858 | GGCGTGAGCCACCGC[A/G]CCCGGCTGAAAAATT | 51444 |
| rs567143283 | snp | A/G | 0.000224115 | 0.0105833 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092732 | CGCCACCGTCACCTC[A/G]GCCGCTGCCGCTGTC | 51444 |
| rs567153206 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129719 | GAAAATTGTATTTAT[A/G]TAACATTTACTATTT | 51444 |
| rs567290807 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | RNF138 | GRCh38.p7 | 18:32126872 | CTTTTTTGTAATCGA[C/G]TTAAATTTTGTGGCA | 51444 |
| rs567439925 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120464 | AAGCAAGACATAACT[A/G]TGGGAAAATAATTTT | 51444 |
| rs567483037 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32121961 | GCAACCTCCGCCTTC[C/T]GGTTTCAAGCGATTC | 51444 |
| rs567501634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115860 | TTCTTGGTTATCCAT[C/T]GTTGCATCACATGCC | 51444 |
| rs567513315 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103228 | TAACTCTGTTGCCCA[C/G]GCTGGAGTACAGTGG | 51444 |
| rs567545493 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095214 | TTATTCTGTTGTCCA[-/G]GGTGGAGTGCAGTGG | 51444 |
| rs567614913 | in-del | -/TT | 0.0197687 | 0.0974348 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129876 | TTGATAATTTCAGTC[-/TT]TGACTGATTTGTAAG | 51444 |
| rs567671053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122305 | CATTGTTGTATACAC[A/G]TTTATTATGAAAGTA | 51444 |
| rs567692227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116470 | AAGAATTGAGTTTGT[A/G]TGTGGATTTTTAGTC | 51444 |
| rs567759218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32097534 | TGTTGCCCAGGCTGG[A/G]GTGCAGTGGTGGGAT | 51444 |
| rs567783852 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126289 | AATTTTCCAGTTTAC[C/T]TCATTTTTATTTTAC | 51444 |
| rs567807642 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32123650 | TAGCTTTTTAAATTA[A/C]ACTTTTTTTTTTTTT | 51444 |
| rs567936360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32102753 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 51444 |
| rs567936739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109625 | GGGCACCATGGCTCA[C/T]GCCTGTAATCCCAAC | 51444 |
| rs568043469 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32118701 | GGGCGTGGTGGTGCG[C/T]GCCTGTAATCCCAGC | 51444 |
| rs568071207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117994 | TGGTCTGTTTTCAGG[C/T]TGTTCTTACTAATCT | 51444 |
| rs568222952 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106281 | TAAGTTTTAGTGTGC[A/C/G]GGTATGCAGAATGCC | 51444 |
| rs568336126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32094506 | AATGTTTTGAGGGAT[C/T]CTTTTGCGGTTCATA | 51444 |
| rs568354515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32126268 | CTAAGGATACAATTT[A/G]AAGTAAATTTTCCAG | 51444 |
| rs568386725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105853 | AACAGATAGCTTTCT[A/G]TGTGACTTTTTTCCC | 51444 |
| rs568388648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32112150 | TTCATAATACTTAGC[A/G]TGGCATTTTTCTAAA | 51444 |
| rs568447301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32100896 | AGGCCTGAGCCACTG[C/T]GCCTGGCCTGAGATA | 51444 |
| rs568472416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32117169 | GGCCTCCCAAAGTGA[C/T]GGGATTACAGGCATG | 51444 |
| rs568492199 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090007 | TTCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCGG | 51444 |
| rs568495352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127205 | TTCTCAAATCTAGCA[C/T]GTAAGACACAACGTT | 51444 |
| rs568595277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113961 | GATGTGTGTGTGTGT[A/T]TGTGCACATGTGTTT | 51444 |
| rs568710660 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32116738 | TTGATTTTTTGGGGT[G/T]GGGGGGTGGTTTTTG | 51444 |
| rs568749356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32117121 | TGGACAGGATGGTCT[C/T]GAACTCCTGACCTCA | 51444 |
| rs568750864 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32120518 | TTGAATTTTATTGGT[A/G]TTTCTGTATCTGATA | 51444 |
| rs568778735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127973 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 51444 |
| rs568805751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097335 | TGTTTTTGCTTTTAG[G/T]CCTCTCTGTAAGGAG | 51444 |
| rs568820003 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129872 | GCATTTGATAATTTC[A/G]GTCTTTGACTGATTT | 51444 |
| rs568842894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096517 | ATATAAATGGAAAGA[C/T]TGAAGAGCACCTAGA | 51444 |
| rs569027536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32123738 | GCTCACTGCAACCTG[C/T]GCCTCTCAGGTTCAA | 51444 |
| rs569033310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32110369 | CTACTATTTATTGAG[C/T]ACTTTCCTGACCATG | 51444 |
| rs569061117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104620 | ACAACATATCTTTAT[A/G]CCAGCAGTAATCAGA | 51444 |
| rs569451925 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092080 | CCCGTTAGGGGCCGA[C/T]AAGCACAGCGCACGC | 51444 |
| rs569481844 | snp | C/T | 0.000160552 | 0.00895826 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092686 | ATCCCCCTCCCCCCT[C/T]CGGGTTCATGTAGGG | 51444 |
| rs569536741 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091789 | CAGGAGAGGTAACTG[C/G]GGTCCCGGGCCTAGC | 51444 |
| rs569678049 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32101011 | TAGTGGGTGAGTATC[A/G]ATGACCCTTTCTTTA | 51444 |
| rs569833776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101451 | TTGGCCAGATTGGTC[C/T]TGAACTCCTGACCTC | 51444 |
| rs569847152 | in-del | -/CTCCCGCTCTCCCGCT | 0.0345262 | 0.126772 | intron-variant | RNF138 | GRCh38.p7 | 18:32093106 | CCCCCTCAGCCCAAG[-/CTCCCGCTCTCCCGCT]CTCCCGCTCTCCCGC | 51444 |
| rs570017109 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095292 | CTCCCGCCTCAGCCT[C/T]TCAAGTTGCTGGGAC | 51444 |
| rs570062971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128884 | TCTGTGATGATCCTC[C/T]CTGTTTGTTTGTTAT | 51444 |
| rs570071052 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120032 | TAGTTTTGTCTGCTT[C/T]TTTTAAACCTAATGT | 51444 |
| rs570264526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105499 | GATAGACGTGACATT[G/T]CAAATGAATGAGGAA | 51444 |
| rs570287932 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121178 | TCCAAATGGAAGATG[C/T]ATGCCATAGGATAAA | 51444 |
| rs570314119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32107176 | CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCGG | 51444 |
| rs570397448 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32117764 | GGATGTTTTAGCAAA[-/ATT]ATTGCATTGGTGTGG | 51444 |
| rs570460869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124631 | GAATAGTCTAATAAT[C/T]ATAACTTTTTTAAAA | 51444 |
| rs570510583 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32105394 | CCGCACTGGCCAAAT[C/G]GTATGGTGTTCATTC | 51444 |
| rs570520416 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092028 | GCTGCTGGCGGCGGC[A/G]GGCGAATCTCCCTGC | 51444 |
| rs570548282 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131364 | TTATGGAAATTAAAT[C/T]TATGGGGAAAAGTTT | 51444 |
| rs570592632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099558 | CAGGCATGCACCACT[A/G]TACCCGGCTAATTTT | 51444 |
| rs570711078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32119548 | TCTGCCTCAGACTCC[C/T]GAGTAGCTGGGACTA | 51444 |
| rs570744344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112433 | CTCATGCCTGTAATC[C/T]CAGCACTTATGGGAG | 51444 |
| rs570746635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120323 | ATCTGGCTAGAGTTC[C/T]AGATATTCTGATATC | 51444 |
| rs570781835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32118684 | AAATAGAAAAATTAG[C/T]TGGGCGTGGTGGTGC | 51444 |
| rs570877788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32102630 | ATTTTGGAGGTTAAT[C/T]TGGGATTTTCTTTTT | 51444 |
| rs570902620 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117782 | ATTGCATTGGTGTGG[G/T]GTAGTTTCTCATAAT | 51444 |
| rs570914596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32096457 | TGTAGATCTGGAATA[C/T]ATGGAGCTAAAGCTG | 51444 |
| rs570954132 | snp | A/T | 1.69218e-05 | 0.00290871 | intron-variant | RNF138 | GRCh38.p7 | 18:32126819 | AGTGAATTCTTCAAG[A/T]TTAAGAAAGTACTGT | 51444 |
| rs570988515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102103 | ACCCAGAATGGCCTC[A/C]AACTCCTGGACTCAA | 51444 |
| rs571101003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32122335 | AAACAGAAAAGAAAG[A/G]TCAGCTGCTAAGTAG | 51444 |
| rs571137284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126220 | GGACAACAGTGAGAC[C/T]GTGTCTCTAGTTTTA | 51444 |
| rs571424632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32116646 | AGCCTTGACCTCCTG[A/G]GCTCAAGCAGTCCTT | 51444 |
| rs571437747 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095156 | TTAGTGGGGGAATTG[A/G]AGAGAAATTTTAAAA | 51444 |
| rs571438889 | in-del | -/C | 0.00795532 | 0.062565 | intron-variant | RNF138 | GRCh38.p7 | 18:32104253 | CTGAGGTCAAATGAT[-/C]CCCCCCACTTCGGCG | 51444 |
| rs571452494 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129834 | GAAGGAAATACAAAG[A/C]GAAAAATTTCTTTCT | 51444 |
| rs571467710 | in-del | -/ATC | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130263 | TCACAGTGCTAAGTT[-/ATC]ATCTAGTTGGCTACT | 51444 |
| rs571503612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109808 | GGAAAATTACTTGAG[C/T]CCTGGAGGCAGAGGT | 51444 |
| rs571556770 | in-del | -/GCCTCAAGTAATCCTCCC | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32108897 | ATGTTGTCCAGGCTG[-/GCCTCAAGTAATCCTCCC]GCCTTGGCCTCCCAA | 51444 |
| rs571604684 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127254 | TAGTTATCAGGCAAA[A/G]CCAGGTTACAAAGAG | 51444 |
| rs571836860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098027 | GTCTCACTGTGTTGC[C/T]CAGGCTGGATTGCAG | 51444 |
| rs571890726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32104249 | AACTCCTGAGGTCAA[A/G]TGATCCCCCCACTTC | 51444 |
| rs572026508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105975 | TATGACACAAGGTGC[C/T]CAACATTCATTCTTC | 51444 |
| rs572112464 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF138 | GRCh38.p7 | 18:32093698 | GGAGAACACAAAGGG[A/G]TTGGGTGAGATAACG | 51444 |
| rs572113123 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32099760 | TTTTGGAATCAGATA[A/C]TTTGACCAATGTCAG | 51444 |
| rs572190083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32105560 | GGGCAATAGCTTTAT[A/T]TGTAGAATCTCTGCT | 51444 |
| rs572255831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125931 | TGTTCCAGGAAATCT[C/T]GCTCATATTTAAGAT | 51444 |
| rs572304063 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107763 | ACCTTGTTATCCACC[C/T]GCCTCAGCCTCCCAA | 51444 |
| rs572395581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112539 | AAAAATAAAAAATCA[G/T]CCAGGTGTGGTGGCG | 51444 |
| rs572461770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120654 | ATGATACAAGGATGA[C/T]TAGGAAGAACTAGAA | 51444 |
| rs572488879 | in-del | -/G | 0.00438332 | 0.0466095 | intron-variant | RNF138 | GRCh38.p7 | 18:32119815 | AACCTTATAGTTTTT[-/G]TTGCTATAAAAATGA | 51444 |
| rs572520004 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113031 | CGAGAGATTCTGGCT[A/G]TTCCTCTCAGTGAGA | 51444 |
| rs572535605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109419 | TTACAGGTGTGAGCC[A/C]CTGTGCCTGGCCATT | 51444 |
| rs572654440 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF138 | GRCh38.p7 | 18:32103729 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 51444 |
| rs572666001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32107302 | ATTTTTTTTTGTATT[C/T]TAGTAGAGACGGCAT | 51444 |
| rs572678725 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101670 | TTAACTGCTATTTTC[A/G]TAAATGTCATGTTGC | 51444 |
| rs572712996 | in-del | -/A | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130416 | CACTACTTTTTAGTT[-/A]AAATTGGGTATGTTC | 51444 |
| rs572868963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32123124 | ATACCATGTCCTAGT[C/T]TGAAGTAAAAAAGTT | 51444 |
| rs572937945 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130087 | ATGTATATATACATA[C/T]ACTTTTGTGTGTATA | 51444 |
| rs572974682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32122515 | CTACTATTGAAAGAC[A/G]TTGCTTTTATAAAAT | 51444 |
| rs572977836 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098218 | GTTTTGAACTCCAGG[C/G]TGGTTTTGAACTCCT | 51444 |
| rs573105882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109951 | GCATCTTGTTTACTT[C/T]GCGTTATTTTGGTTT | 51444 |
| rs573144326 | in-del | -/TGTTTC | 0.00279162 | 0.0372561 | intron-variant | RNF138 | GRCh38.p7 | 18:32120517 | ATTGAATTTTATTGG[-/TGTTTC]TGTATCTGATAAAAT | 51444 |
| rs573163527 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126967 | TTTAGCTTGTAGAAA[C/T]GGTAAGGTAAAAATT | 51444 |
| rs573192914 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106437 | ATTCTATTTGTCATT[C/T]GTTATTGCTCATGAG | 51444 |
| rs573202254 | snp | A/G | 1.65362e-05 | 0.00287538 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124827 | TAACAGTAATCACCT[A/G]TTTCAGATAGTTCCT | 51444 |
| rs573273752 | in-del | -/T | 0.189576 | 0.242588 | intron-variant | RNF138 | GRCh38.p7 | 18:32116516 | AAAGGAAGGAAAAGC[-/T]TTTTTTTTTTTTTTT | 51444 |
| rs573299238 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110925 | AGCTGAAACTACAGG[C/T]GCCTGTCACCACGCC | 51444 |
| rs573414138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32111170 | ACCAAATAACCAAAT[A/G]TCTGTTAACACGCAG | 51444 |
| rs573463347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117433 | GGAAATAGATAACAG[A/T]ACCTGAAGAAGAGAG | 51444 |
| rs573555885 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109111 | TGGTTCATATCCTCC[C/T]TAACACTTGGTATTT | 51444 |
| rs573567205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32127714 | AGATTGCTATGTAAT[C/G]TATTTGGAAATACAA | 51444 |
| rs573612825 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118437 | TACTCAGGAGGCTGA[G/T]GCAGGAGAATTTCTT | 51444 |
| rs573630784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101093 | GAGGGCTGTGCTCGT[A/G]CATAGAACATTCTGG | 51444 |
| rs573686602 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091417 | AAAATAAAATAAAAT[A/T]AAATAAAATTAAAAA | 51444 |
| rs573746870 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF138 | GRCh38.p7 | 18:32121144 | GTCTCAAAAAAAAAC[A/C]AAACAAAAAAAAAGC | 51444 |
| rs573768048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32113269 | TGCCATATTGCTCAG[A/G]CTGGTCTTGAACCCC | 51444 |
| rs573780875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32114546 | CTGCCCATTTGAACC[A/G]TACACTCCTAGATGC | 51444 |
| rs573885164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120872 | GTACTGGCTGGGGGC[A/G]GTGGCTCATGTCTGT | 51444 |
| rs574036397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32101788 | TTAAGCATTTTTATG[C/G]TATTTTAATACAGTT | 51444 |
| rs574093166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115244 | AGACAGGCCTTCCTC[C/G]CCCTTATTTCTTAGA | 51444 |
| rs574119875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32102351 | GGACTACAGGCGCCC[A/G]CCGCCACGCCCGGCT | 51444 |
| rs574195196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32108187 | GTATAAAATGCATAC[A/G]GAAACGTGTCCCTAT | 51444 |
| rs574242249 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093462 | AACACCCTCGAGAGC[A/G]TTTTGTTTCGTTTCC | 51444 |
| rs574247869 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121468 | CCACTGCATTCCAGC[C/T]GGGGCAATAAGAGCG | 51444 |
| rs574260704 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129417 | AAAAGATGTTTCACT[A/C]ATGTAACGGTGAAAG | 51444 |
| rs574383053 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090973 | GATTTATCCTTTTTT[C/T]GTTCTTCTTTTTTTT | 51444 |
| rs574386556 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32098403 | GTCCTCCCACCTGAG[C/T]CTCCTGAGTAGTGGG | 51444 |
| rs574449941 | in-del | -/T | 0.288127 | 0.247076 | intron-variant | RNF138 | GRCh38.p7 | 18:32115013 | TTGTTGCTCTTATAG[-/T]TTTTTTTTTAGTCCT | 51444 |
| rs574588628 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112554 | GCCAGGTGTGGTGGC[A/G]CATGCCTATAATCCC | 51444 |
| rs574644149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106706 | AGTAGCTGGGACTAC[A/G]GGCGCCCGTCACCAT | 51444 |
| rs574700488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32099089 | CTTTTGTTGGGAGAA[C/T]GCGTAATGGAAATTC | 51444 |
| rs574731311 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32107233 | TTAAGCAGTTCTCCT[G/T]CCTCAGCCTCCTGAG | 51444 |
| rs574788727 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32102359 | GGCGCCCGCCGCCAC[A/G]CCCGGCTAATTTTTT | 51444 |
| rs574807447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32125091 | ACAGTCTGGAGAAGA[C/G]TGAAGTAATGAAAGA | 51444 |
| rs574808536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32112473 | GGTGGATGACCTGAG[G/T]TCAGGAGTTCGAGAC | 51444 |
| rs574860029 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096758 | TTTTTTTGAAATAGG[A/G]TCTCGCTCTGTTGCG | 51444 |
| rs574862270 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127691 | TTATTAAATTCTCAT[A/T]GTAAGAAAGATTGCT | 51444 |
| rs575000776 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124291 | TAGGGCCTGGTATTT[A/G]TTAGAGATACGATAT | 51444 |
| rs575015191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32100767 | AGGCGTGAGCCCCCG[C/T]GCCCGGCCTGTATTT | 51444 |
| rs575094049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109394 | CCGCTCAGCCTCTCA[A/G]AGTGCAGGATTACAG | 51444 |
| rs575114081 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101415 | TATATATTTTTAAAT[C/T]AGAGTCAGGGTTTCA | 51444 |
| rs575169609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32115613 | AGCTGGACGTGGTGG[C/T]GCGTGCCTATAGTCC | 51444 |
| rs575183351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32108882 | GAGCAAAGTCTCACT[A/G]TGTTGTCCAGGCTGG | 51444 |
| rs575183591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116080 | ATGATGATAGGTCCT[C/T]ATTGAGTTGAAGTTA | 51444 |
| rs575195569 | in-del | -/AAG | 0.00236616 | 0.0343144 | intron-variant | RNF138 | GRCh38.p7 | 18:32112689 | CGCTGTCTAAAAAAA[-/AAG]AAGAAGAAAGAAATC | 51444 |
| rs575256883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128421 | TACGTATCTGTAATC[C/G]TAGCTACTTGGCAGG | 51444 |
| rs575291848 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129333 | GAAAATAAAGGTAGG[A/G]CTTCTAAAAACTTCA | 51444 |
| rs575386755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102861 | GTCTTGAACTCCTGA[C/T]CTTAGGTGATCCACC | 51444 |
| rs575499533 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131802 | CAAGATTTTCAAGCC[C/T]TGTTAGCAGCTAGGC | 51444 |
| rs575556413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32097651 | GTAGCTGGACTACAG[A/G]CATGCACCACCATGC | 51444 |
| rs575672062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096869 | GTAGCTAGCTGGGAC[C/T]ACAGGCACTCACCAC | 51444 |
| rs575712235 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091337 | AGGTTGGACCATCTT[A/T]TAGATTATCAATTGT | 51444 |
| rs575785583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32124125 | CCACACACGATTCAG[C/G]TAAAGTTGTCTGTGT | 51444 |
| rs575822898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117416 | GAAAGCAGGAGAGAG[A/G]AGGAAATAGATAACA | 51444 |
| rs575907519 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF138 | GRCh38.p7 | 18:32100624 | GGGATTAAAGGCATG[C/T]GCCACCAGGCCTGGC | 51444 |
| rs576066507 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF138 | GRCh38.p7 | 18:32093132 | CCGCTCTCCCGCTCT[C/T]CCGCTCTCCCGCTCT | 51444 |
| rs576075713 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF138 | GRCh38.p7 | 18:32106596 | TTGAGATGGAGTCTC[A/G]CTCTGTCACACAGGC | 51444 |
| rs576152426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32093942 | GTGGGGCCTGGAAAT[A/C]TTTATTTATTTATTT | 51444 |
| rs576172808 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RNF138 | GRCh38.p7 | 18:32111314 | CATGTCGATATACAT[A/C]AGTTTGAGACAAAAG | 51444 |
| rs576189333 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095459 | TGACAGGCGTGAGGC[A/C]TGGCACCTGACCTGT | 51444 |
| rs576276484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096033 | GGTACAGAGGATGAA[A/T]GTGAGCTGGACTTTG | 51444 |
| rs576315162 | in-del | -/GT | 0.00199481 | 0.0315187 | intron-variant | RNF138 | GRCh38.p7 | 18:32129003 | ACATAACTGTCCTGA[-/GT]GTGTGTAATGTGTGT | 51444 |
| rs576332732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32126539 | ATCTAAGGTAATTGA[C/T]TGGGAAATGATCTAG | 51444 |
| rs576384077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107462 | TCCTTTTTTAAATTT[C/T]AGCAGTTTTTTTTTA | 51444 |
| rs576394758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32107954 | CCACCTCCCAGGTAC[A/G]AGTGATTCTCCTGCC | 51444 |
| rs576419476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF138 | GRCh38.p7 | 18:32101295 | GCAGTCTTGGCTCAC[G/T]GTAACCTCCGCCTCC | 51444 |
| rs576575992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32120784 | TAAATCAGAAGTTTT[G/T]TGATTGCATTACCCT | 51444 |
| rs576587750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32098291 | GATTACAGGTGTGAG[C/T]CACTGCGCCCACAAT | 51444 |
| rs576632438 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091910 | AGGCCGCACTTCACA[C/T]CCCGTGCCTCCCCGC | 51444 |
| rs576678173 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117655 | ATCTAACTGTAAGCT[A/G]TAACTTCCAGTTGAG | 51444 |
| rs576757114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32110130 | AGCTGGGACTGGACG[C/T]GCATGCTACTATACC | 51444 |
| rs576789752 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108064 | TTTGCCATGTTGGCC[A/G]GGCTGGTCTTGACCT | 51444 |
| rs576814109 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115819 | CCCTTTCTGATCTGG[C/G]CCTTTCCTCTCTTTT | 51444 |
| rs576903606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32117287 | GTGGGCTCTAATTAT[A/G]CGATTTGAGGAGAAT | 51444 |
| rs576991550 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101873 | CTGCATGCATTTTTC[C/T]ATATTACATTTTTGC | 51444 |
| rs577019758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32116889 | CACGCCTGGCCAGAA[A/G]TGTTTATTTTTATTT | 51444 |
| rs577077254 | snp | A/G | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131679 | GGATAAGAAAAAGCT[A/G]CCACATGCTGGTGCT | 51444 |
| rs577204401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128313 | GAGGCCGAGGCGGGT[A/G]GATCACCTGAGGTCA | 51444 |
| rs577209937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32128792 | GTTGCAACTACAGGC[A/G]CATGCTTACCCAGCT | 51444 |
| rs577223668 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114836 | GCACTTCATGTTGAT[C/G]ATACTACATTAGGCG | 51444 |
| rs577297794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32095371 | GAGACAGGGCCTCAC[C/T]ACGTTGCCCAGTCAG | 51444 |
| rs577399641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32106121 | CTTCTTTTAAAAAAA[A/T]TTTAGGGTGAAGTGT | 51444 |
| rs577488367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32121302 | GGAGTTTGAGACCAG[A/C]CTGACCAACATGGAG | 51444 |
| rs577924066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102780 | TGGGATTACAGGTGC[A/G]CAACACCACGCCCAG | 51444 |
| rs578039006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096215 | TTGGCAGGGGAGCAG[C/T]GTGGTCACATTTCAT | 51444 |
| rs578061056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32109359 | GCCCAGGCTGGTCTT[A/G]TGAGCTTAAGCCATT | 51444 |
| rs578103041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32096781 | CTGTTGCGAGGAGTG[C/T]AGTGGCATGATCATA | 51444 |
| rs578157892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF138 | GRCh38.p7 | 18:32102393 | TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTA | 51444 |
| rs578165143 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090252 | TTCTGTCTCAAAAGA[A/T]AAAAGAAAAAAAGTG | 51444 |
| rs578186496 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096071 | GCTGGAGCCAAAGAC[A/G]GCGTAGTGGAGATGG | 51444 |
| rs578204081 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091013 | CACTCTGTCGCCAGG[A/G]CTGGAGTGCAGCGGC | 51444 |
| rs745311557 | snp | A/C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093668 | AGCCGAAATTGAGAT[A/C/G]CTACCCAGGGTGGGG | 51444 |
| rs745343222 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128794 | TGCAACTACAGGCGC[A/G]TGCTTACCCAGCTTT | 51444 |
| rs745559710 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127828 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 51444 |
| rs745611799 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100765 | ACAGGCGTGAGCCCC[C/T]GCGCCCGGCCTGTAT | 51444 |
| rs745681733 | snp | C/T | 8.85387e-05 | 0.00665293 | intron-variant | RNF138 | GRCh38.p7 | 18:32092908 | AGACGCCCCCTCCCC[C/T]TCGCGGAGCCGGGTT | 51444 |
| rs745696010 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104013 | AATAGGCTAAAAAAC[-/TT]TTTTTTTTTTTTTTT | 51444 |
| rs745806300 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099429 | TTATTTTTAGACAAA[A/T]TCTCGCTCTGTTGCC | 51444 |
| rs745916035 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126198 | TCAGGAATTTGAGAC[C/T]CAGCCTGGACAACAG | 51444 |
| rs745963692 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100629 | TAAAGGCATGCGCCA[A/C]CAGGCCTGGCTAATT | 51444 |
| rs746015735 | in-del | -/TAAG | 5.14275e-05 | 0.00507061 | intron-variant | RNF138 | GRCh38.p7 | 18:32124703 | TGTGTTATTCTGAAT[-/TAAG]TATGTTTCACTTAAA | 51444 |
| rs746029955 | snp | A/G | 2.80344e-05 | 0.00374385 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092655 | CCCTTCCTGGCGCGC[A/G]CTGTATCCTGATGCG | 51444 |
| rs746093685 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112590 | CTTGGGAGGCTGAGG[A/C]AGAATTGTTTGAACC | 51444 |
| rs746148870 | snp | C/T | 3.50324e-05 | 0.00418509 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092734 | CCACCGTCACCTCGG[C/T]CGCTGCCGCTGTCGC | 51444 |
| rs746176630 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105805 | GATGGACTGAATGTC[A/G]TCTGTTCTACTTGCT | 51444 |
| rs746266092 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090935 | CTTAGCTTCTTTCAC[A/G]TCATTGTGGATCCCA | 51444 |
| rs746292768 | in-del | -/CTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127174 | GTTGCTTGTATTATG[-/CTA]CTAGAAATCTTAGAT | 51444 |
| rs746388348 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119465 | AGTCTAACTCTGTCT[C/G]TCAGGCTGGAGTGCA | 51444 |
| rs746433990 | snp | G/T | 5.03343e-05 | 0.00501643 | intron-variant | RNF138 | GRCh38.p7 | 18:32123602 | AAAATCCTGCCACTT[G/T]AGCAAGTAATATTAT | 51444 |
| rs746549917 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100845 | CCTGAGCTCAAGCGA[A/T]CTGCTCGCCTTGGCC | 51444 |
| rs746557046 | snp | A/G | 1.8872e-05 | 0.00307175 | intron-variant | RNF138 | GRCh38.p7 | 18:32113889 | ATTCCTAAATACAGA[A/G]TTTTCATAATTGAAA | 51444 |
| rs746580840 | snp | A/T | 1.66639e-05 | 0.00288646 | intron-variant | RNF138 | GRCh38.p7 | 18:32123584 | TACAAGGTAAGCTTT[A/T]GAAAAATCCTGCCAC | 51444 |
| rs746587797 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117562 | TTCATACTGTTTATT[A/G]TACGTTCTGAAGTGC | 51444 |
| rs746675179 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130575 | GAAGAACATAAAAGA[A/G]AGAGAATCTCAGAAG | 51444 |
| rs746840222 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125697 | AGCACTTTGGGAGGC[C/T]GAGAGGGGAGGATTG | 51444 |
| rs746946664 | in-del | -/AAA | 1.67167e-05 | 0.00289103 | intron-variant | RNF138 | GRCh38.p7 | 18:32123501 | GGTATTAACTTTTTC[-/AAA]CCCTGTGCTTCTTAA | 51444 |
| rs746972468 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102723 | CTGAAACCTCCATCT[C/T]CCAGGTTCAAGTGAT | 51444 |
| rs747132487 | in-del | -/TGTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097975 | GTGTGTGTGTGTGTG[-/TGTT]ATTTTTGTTTGTTTG | 51444 |
| rs747146338 | in-del | -/AG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095820 | GTGCAGGGACTACTA[-/AG]TACTGTTTCTCTGGA | 51444 |
| rs747164148 | snp | C/T | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129153 | AAACCCAATACCAAA[C/T]TGCTGTTGAAGAATC | 51444 |
| rs747241245 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098089 | CCTCCCTGGTTCAAG[C/T]GATTCTACTCCCTCA | 51444 |
| rs747340018 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106074 | TTTAAATTTATTTCC[A/G]TAATTTAACAGCTTC | 51444 |
| rs747342391 | snp | C/T | 0.000978952 | 0.0221024 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092650 | CCGCCCCCTTCCTGG[C/T]GCGCGCTGTATCCTG | 51444 |
| rs747450816 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093909 | CATTTCAAACTTAAC[A/G]AAAGAATGTTCGGGC | 51444 |
| rs747528665 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107643 | CTCCTACCTCAGCCT[C/T]CCAAGTAGCTAGGAT | 51444 |
| rs747543940 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116835 | GTGATCCACCTGCCT[-/C]TGGCCTTCCAAAGTG | 51444 |
| rs747664225 | in-del | -/TAACTTTGGGTAACACC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111187 | CTGTTAACACGCAGA[-/TAACTTTGGGTAACACC]TAACTTTGGGTAAAA | 51444 |
| rs747736592 | snp | A/T | 5.40906e-05 | 0.00520023 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113752 | ATTTACAGATTAAAT[A/T]CTATCGCATGAGACA | 51444 |
| rs747813264 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117665 | AAGCTATAACTTCCA[G/T]TTGAGCCATCTAAAA | 51444 |
| rs747859034 | snp | A/G | 1.77219e-05 | 0.00297668 | intron-variant | RNF138 | GRCh38.p7 | 18:32113868 | GGGAACAGGTAAGCA[A/G]TACTTATTCCTAAAT | 51444 |
| rs747862394 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127027 | AGAGAATTAATAAGA[A/G]TAACAGCAAGCACCC | 51444 |
| rs747864340 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127544 | TGTTGAAATTACATC[A/G]TTCTTGTTAAATGGT | 51444 |
| rs747936537 | in-del | -/A | 1.81095e-05 | 0.00300906 | intron-variant | RNF138 | GRCh38.p7 | 18:32113873 | AGGTAAGCAATACTT[-/A]ATTCCTAAATACAGA | 51444 |
| rs747943159 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112639 | GTGAGCTGAGATTGC[A/G]CCATTGCACTCCAAA | 51444 |
| rs747949981 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114124 | TTTTTTTGAGTAAAA[A/G]ATAAGTTGGAGATTT | 51444 |
| rs748137313 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125824 | TGAGGATGACCTTAA[A/G]CTCTCACATACCACC | 51444 |
| rs748204194 | snp | A/G | 1.6896e-05 | 0.0029065 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111782 | TGTTTCCTGACTGCA[A/G]TGAGGGAAAGCGGAG | 51444 |
| rs748224904 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122435 | TCTGGCATTGAGATA[C/T]AGAACCAACCTGTAT | 51444 |
| rs748268521 | in-del | -/TGTGTTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097973 | GTGTGTGTGTGTGTG[-/TGTGTTA]TTTTTGTTTGTTTGT | 51444 |
| rs748314997 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109615 | TAGTTTTGCTGGGCA[C/T]CATGGCTCACGCCTG | 51444 |
| rs748391443 | in-del | -/TTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096673 | ATCATCTGCAAATGA[-/TTG]TTAAGGAAGCAGTCA | 51444 |
| rs748438666 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131112 | TTAAACCATTCTGGG[A/G]TTTGGGAACTTCTTT | 51444 |
| rs748454038 | snp | C/T | 6.60077e-05 | 0.00574452 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126752 | GATTACCAGAAATTT[C/T]GTTAGTCATCTAAAT | 51444 |
| rs748474741 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126858 | TAAAGTTAAAATAAC[-/TT]TTTTGTAATCGACTT | 51444 |
| rs748495982 | snp | C/T | 6.59783e-05 | 0.00574324 | intron-variant | RNF138 | GRCh38.p7 | 18:32129109 | TTGACATGAATGTTA[C/T]TGTTTTTAGAATCTT | 51444 |
| rs748661093 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094055 | CTCGGCCTCCCAAAG[C/T]GCTGGGATTAAAGGC | 51444 |
| rs748756050 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090790 | AATGGCAGAATTGAT[A/T]TAAATAGTCCCTTAA | 51444 |
| rs748776635 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108929 | CGCCTTGGCCTCCCA[A/G]AGTGCTGGGATTATA | 51444 |
| rs748861335 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127635 | GTAAAATTTAGGTGC[A/G]CTTTATTGCTTTAGC | 51444 |
| rs748939391 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111053 | CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC | 51444 |
| rs749075433 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098187 | GAGACAGGGTTTTAC[C/G]ATGTTGGCCAGGCTG | 51444 |
| rs749081700 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099290 | TTCTGTCTAGCACTT[C/T]GATCCATTCCAGCCC | 51444 |
| rs749173549 | in-del | -/TC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106108 | CACTTATCCCTCTCT[-/TC]TTTTAAAAAAATTTT | 51444 |
| rs749182385 | in-del | -/TACTT | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131244 | TTTTCATAAGGAAAA[-/TACTT]TACTTTATTTGCTTT | 51444 |
| rs749234351 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128523 | AGCCTGAGTGACAGA[A/G]CCAAACTGCCCCCCA | 51444 |
| rs749263568 | in-del | -/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110139 | GGACGTGCATGCTAC[-/TA]TATACCCAGCTAATT | 51444 |
| rs749324887 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119851 | CTTTTTTTCCTGTTT[G/T]ATAATCTAATTAGTT | 51444 |
| rs749363539 | snp | C/T | 3.32729e-05 | 0.00407864 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092769 | GCCTTGTTTCCCCAT[C/T]CCCCGCCATGGCCGA | 51444 |
| rs749379801 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112357 | AGGAACTCTCTAGCT[C/G]CTCACTTTACTTATG | 51444 |
| rs749537684 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123872 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 51444 |
| rs749582178 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117848 | CCTATTTTATAACAA[C/T]ATTCTGCTGCTAACA | 51444 |
| rs749645621 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123873 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 51444 |
| rs749646408 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126470 | ATTTGTGTAATAAGA[A/G]ATTTAAGGAATAGAA | 51444 |
| rs749694393 | snp | C/T | 1.76104e-05 | 0.00296731 | intron-variant | RNF138 | GRCh38.p7 | 18:32124684 | AATAGGAGAGCGTTA[C/T]TTTTGTGTTATTCTG | 51444 |
| rs749723796 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119346 | ATCAAACAGTCCTCC[C/T]GCCTTGGCCTCCTAA | 51444 |
| rs749732969 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103168 | GTAAAAATTCATTCA[A/G]CATTTGTTTATTTTT | 51444 |
| rs749751834 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096548 | TAGAGCCAAGTGTTG[G/T]AGAATACTTACTTAA | 51444 |
| rs749990975 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094833 | AATCATTCTAATTAT[C/T]CTTTGGGTCATTGAC | 51444 |
| rs750007597 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130405 | AACCACTGTTTCACT[A/G]CTTTTTAGTTAAAAT | 51444 |
| rs750039218 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108843 | CCAGCTAATTTTTTA[C/T]TTTTATTTTTAATTT | 51444 |
| rs750136806 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117516 | AGTAGAAAAAAAAAT[G/T]GCAAAATAAATCCAT | 51444 |
| rs750243422 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119338 | CTCTGGGGATCAAAC[A/G]GTCCTCCCGCCTTGG | 51444 |
| rs750291050 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130723 | AATTTTGGAAGTGCA[-/G]TTTTGTAAAAACCTT | 51444 |
| rs750294722 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122565 | GCGGTGGCTCACACC[G/T]GTAATCGCAGCAGTT | 51444 |
| rs750298913 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097981 | TGTGTGTGTGTTATT[-/G]TTTGTTTGTTTGTTT | 51444 |
| rs750316425 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120798 | GTGATTGCATTACCC[-/T]TATCAGTGAAAGAAT | 51444 |
| rs750316581 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095771 | AATCCCCATTCATTC[C/T]CTGAAACTGCAGTTG | 51444 |
| rs750428857 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128274 | TGGGCATGATGGCTC[A/G]TGCCTGTCATCCCAG | 51444 |
| rs750489572 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113416 | TGCAGAAGTTAAATA[A/G]TAAGACATGCCCAAT | 51444 |
| rs750650094 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108118 | CTCGGCTCCTCAAGG[-/T]TGCTGGGATTACAGG | 51444 |
| rs750670247 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127241 | AAATGAGGGAGCTTA[A/G]TTATCAGGCAAAGCC | 51444 |
| rs750755769 | snp | C/G/T | 7.39761e-05 | 0.00608142 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092869 | AACGCCCGTGCGGAC[C/G/T]ACGGCCTGTCAGCAC | 51444 |
| rs750837382 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122225 | CTATGTGTGGAGAGA[G/T]AACATTGTTATCTTC | 51444 |
| rs750849971 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112591 | TTGGGAGGCTGAGGC[A/C]GAATTGTTTGAACCT | 51444 |
| rs750907729 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32091913 | CCGCACTTCACACCC[C/G]GTGCCTCCCCGCCTC | 51444 |
| rs750963111 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099116 | ATTCGTCTAGCATCT[G/T]CTAGTTTAAAGTTGA | 51444 |
| rs751131042 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096643 | ATAAAGTGAGAGTGG[A/G]AACTGAGGATTCAGA | 51444 |
| rs751170194 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095016 | GGACCTTTCTCAAAT[A/C]AACTTATTGTACGTA | 51444 |
| rs751205866 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111716 | AGATGAAGAGAGTAA[C/T]TTTTTTTGTAATTAA | 51444 |
| rs751265868 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104601 | CAAGAACAGACAAAA[A/G]TCAACAACATATCTT | 51444 |
| rs751288454 | snp | A/G | 6.80203e-05 | 0.00583142 | intron-variant | RNF138 | GRCh38.p7 | 18:32126822 | GAATTCTTCAAGATT[A/G]AGAAAGTACTGTTTA | 51444 |
| rs751316721 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120405 | TTGGATAGAGATCCT[A/G]TTGAATGCAGTAAAC | 51444 |
| rs751413015 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106506 | CTATTTTTACTTCCT[C/T]TCTGGAAGATACTAG | 51444 |
| rs751611531 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099161 | GACCTTTTTTGGTTA[C/T]AGGGTAATGCCCTGT | 51444 |
| rs751628139 | snp | A/C | 1.67609e-05 | 0.00289486 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113837 | TCCAAACTTTCAGAT[A/C]TCTCAAGATTCAGTA | 51444 |
| rs751634527 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100203 | TGTTAGTGATTGAGA[G/T]ATATATATATATATA | 51444 |
| rs751674649 | in-del | -/A | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32089905 | CAGAAAATACACCTT[-/A]ACTTCCTAAATGGTC | 51444 |
| rs751782557 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130100 | TATACTTTTGTGTGT[A/G]TATATACACATATGT | 51444 |
| rs751809651 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115296 | GATTCCTAATAGCAA[C/T]ATTCCTCATCTGTAC | 51444 |
| rs751880745 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123187 | ACCTTACTAGTCTAG[A/G]TAAAGGTAGAGGAAT | 51444 |
| rs751914942 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125036 | AATTGCAGTAACTCT[C/T]ATTATAAAAAGGGAG | 51444 |
| rs751968517 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110937 | AGGCGCCTGTCACCA[C/T]GCCCGGCTAATTTTT | 51444 |
| rs752037549 | in-del | -/T | 0.0274168 | 0.113828 | intron-variant | RNF138 | GRCh38.p7 | 18:32111715 | AGATGAAGAGAGTAA[-/T]TTTTTTTTGTAATTA | 51444 |
| rs752121707 | snp | A/C | 0.000132266 | 0.00813116 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092705 | GTTCATGTAGGGAGT[A/C]GGGCCCCGGGCCGCC | 51444 |
| rs752212769 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119014 | TTCTACATGAAGGTT[A/T]TAAAAGATATTTTCT | 51444 |
| rs752580212 | snp | A/C | 1.65059e-05 | 0.00287275 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124805 | GACAGCGTTTACTGG[A/C]TCACTGTAACAGTAA | 51444 |
| rs752659184 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101541 | GTTTCCTCATCTGTA[A/C]AATGAAGGAACTTAT | 51444 |
| rs752819575 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110319 | TTTATGGTGTTAATT[A/G]GTAATGACTTCTAGT | 51444 |
| rs752918175 | snp | C/T | 1.70194e-05 | 0.00291709 | intron-variant | RNF138 | GRCh38.p7 | 18:32111942 | AAATGTGACATCTCT[C/T]TTCTTTGGAAGCCAA | 51444 |
| rs752971550 | snp | C/T | 3.33289e-05 | 0.00408207 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113819 | TGGTGTTTCTTCTAT[C/T]ATTCCAAACTTTCAG | 51444 |
| rs753047212 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113180 | CAGGCTCTAAGCAAT[C/T]CTCCTGCCTCAGCCC | 51444 |
| rs753060354 | snp | C/T | 1.68156e-05 | 0.00289957 | intron-variant | RNF138 | GRCh38.p7 | 18:32111930 | AACAGGTAGAGTAAA[C/T]GTGACATCTCTCTTC | 51444 |
| rs753102213 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094795 | CTATATATATATATA[A/T]AAAGCAGGTCTTTTT | 51444 |
| rs753433541 | in-del | -/TCA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116161 | AATGTTAGTTCTTCC[-/TCA]TCATCCTCATTATCA | 51444 |
| rs753436891 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108458 | CTTGTTTAGCTCAAC[A/G]TTATATCATTATGTT | 51444 |
| rs753439945 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120730 | AGATAGAAGGGAGAA[C/T]GTGTTTAAAAAGGGC | 51444 |
| rs753471442 | in-del | -/A | 6.08772e-05 | 0.00551678 | intron-variant | RNF138 | GRCh38.p7 | 18:32113699 | ACTATTTCAAATCTT[-/A]ACGAGTTCTATTTTA | 51444 |
| rs753593263 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130305 | AAAATTGAGTTTACA[C/G]ACACACAATTACCTG | 51444 |
| rs753618697 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094725 | CTGTGTTGGCATTGG[A/G]TAGATAAAAGGGAGG | 51444 |
| rs753660399 | snp | A/G | 1.68442e-05 | 0.00290204 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113845 | TTCAGATCTCTCAAG[A/G]TTCAGTAGGGAACAG | 51444 |
| rs753686094 | snp | C/T | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131780 | ATTTTATGAAGTGTC[C/T]GCGGAGCAAGATTTT | 51444 |
| rs753858069 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090143 | CTCAGCTACTTGGGA[G/T]GCTGAGGCAGGAGAG | 51444 |
| rs753885628 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105380 | ACAGGCATGAGCCAC[C/T]GCACTGGCCAAATCG | 51444 |
| rs753933082 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125483 | GTGAATGGAACAGGA[G/T]AAACTGAGCTGGGAG | 51444 |
| rs754020049 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127007 | CTCCACCTCCTGTAC[C/T]AGAGAGAGAATTAAT | 51444 |
| rs754076818 | snp | C/T | 2.09185e-05 | 0.00323401 | intron-variant | RNF138 | GRCh38.p7 | 18:32111739 | GTAATTAATGTGTCA[C/T]AATGTTTGGTTTAGT | 51444 |
| rs754111567 | in-del | -/TTTTTTTTTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100469 | CCACACCCAACTAAC[-/TTTTTTTTTT]TTTTTTTTTTTTTTG | 51444 |
| rs754118002 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090080 | GCAAAACCCTGTCTC[-/T]ACTAAAAATGCAAAA | 51444 |
| rs754185133 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099084 | TTAGCCTTTTGTTGG[G/T]AGAATGCGTAATGGA | 51444 |
| rs754197892 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114844 | TGTTGATCATACTAC[A/G]TTAGGCGTCTTCCCT | 51444 |
| rs754280275 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092316 | CGCGGACACGGGCTG[A/G]GCACTCGGGGCTCGG | 51444 |
| rs754315256 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128880 | TTGTTCTGTGATGAT[C/T]CTCTCTGTTTGTTTG | 51444 |
| rs754471510 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111143 | CTGTTTGGGAAATTT[C/T]CCTACTTCCGGACCA | 51444 |
| rs754554442 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111831 | GTGGAAATGTGACTA[G/T]AAGAGAGAGAGCATG | 51444 |
| rs754560756 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095026 | CAAATCAACTTATTG[C/T]ACGTAGACAGTTCTG | 51444 |
| rs754631199 | in-del | -/AAC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122321 | TTTATTATGAAAGTA[-/AAC]AGAAAAGAAAGATCA | 51444 |
| rs754635640 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100478 | CTAACTTTTTTTTTT[-/TT]TTTTTTTTTTTTTTG | 51444 |
| rs754669973 | in-del | -/AAATTA | 2.9224e-05 | 0.00382245 | intron-variant | RNF138 | GRCh38.p7 | 18:32113714 | TACGAGTTCTATTTT[-/AAATTA]AAAGTCACATTTTAA | 51444 |
| rs754719094 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090816 | CTTAAATGGCTTCTG[G/T]TTATTCATTTAGACC | 51444 |
| rs754773357 | in-del | -/TTTTTTTTTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100473 | CACCCAACTAACTTT[-/TTTTTTTTTT]TTTTTTTTTTTGAGA | 51444 |
| rs754775307 | snp | G/T | 5.06487e-05 | 0.00503208 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113847 | CAGATCTCTCAAGAT[G/T]CAGTAGGGAACAGGT | 51444 |
| rs754783035 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090308 | ATTTGAACTCAAAGA[A/G]CCATTTTATAAGTGA | 51444 |
| rs754800364 | snp | G/T | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091375 | ATTGCACTCCGGCCT[G/T]GGAGACAGAGTGAGT | 51444 |
| rs754816383 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102728 | ACCTCCATCTCCCAG[G/T]TTCAAGTGATTCTCC | 51444 |
| rs754899692 | snp | C/T | 8.30351e-05 | 0.00644288 | splice-donor-variant | RNF138 | GRCh38.p7 | 18:32123576 | CAAGAGAATACAAGG[C/T]AAGCTTTTGAAAAAT | 51444 |
| rs754904719 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118824 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAG | 51444 |
| rs755095445 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115433 | TCTATCGCCAAAGTA[A/T]TATTAATGAAGTATA | 51444 |
| rs755189771 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099167 | TTTTGGTTATAGGGT[A/C]ATGCCCTGTTCTGAA | 51444 |
| rs755196100 | in-del | -/AAGGAGGAAAAGCAAC | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090443 | ACTGCGCTTGCTGCT[-/AAGGAGGAAAAGCAAC]AAGGAGGAAAAGCAA | 51444 |
| rs755256052 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116414 | TGAGCTTTTTAGTCT[C/T]ATTTATTTCTATATC | 51444 |
| rs755319836 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110956 | CGGCTAATTTTTTAT[A/G]TTTTTAGTAGAGACG | 51444 |
| rs755347429 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092376 | TGAAAAGGGAGGCCT[C/T]GGGCGAAGACGGGGG | 51444 |
| rs755422582 | snp | C/T | 0.000164984 | 0.00908101 | intron-variant | RNF138 | GRCh38.p7 | 18:32129106 | CTGTTGACATGAATG[C/T]TATTGTTTTTAGAAT | 51444 |
| rs755473367 | in-del | -/AT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124184 | TATTAAAACTCAGTG[-/AT]GCTTGATCCTCAGAA | 51444 |
| rs755474325 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123344 | TTCATAGTTCAGAAC[C/G]ATTTGAAGTTCAAAT | 51444 |
| rs755477916 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102358 | AGGCGCCCGCCGCCA[C/T]GCCCGGCTAATTTTT | 51444 |
| rs755601820 | in-del | -/ATA | 1.65462e-05 | 0.00287625 | cds-indel, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111875 | TTAGACCTTGAAAAT[-/ATA]ATGAGGAAGTTTTCT | 51444 |
| rs755676559 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105406 | AATCGTATGGTGTTC[A/G]TTCAGCAGTAGATAA | 51444 |
| rs755829551 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093483 | TTTCGTTTCCAGTCC[A/G]CTATGTGTTAGAGGG | 51444 |
| rs755863688 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119952 | TAGTTCTAATCTGGC[A/C]GTTCTTATAATCTAC | 51444 |
| rs755867101 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119020 | ATGAAGGTTATAAAA[C/G]ATATTTTCTTCTTAA | 51444 |
| rs755916483 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095216 | ATTCTGTTGTCCAGG[A/G]TGGAGTGCAGTGGTG | 51444 |
| rs756044993 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106616 | GTCACACAGGCTTGA[A/G]TGCAGTTGTGCGATC | 51444 |
| rs756058198 | snp | A/G | 1.72794e-05 | 0.00293928 | intron-variant | RNF138 | GRCh38.p7 | 18:32111958 | TTCTTTGGAAGCCAA[A/G]TTTCTACTCTGAAAT | 51444 |
| rs756089669 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127565 | GTTAAATGGTTTTTA[A/T]ATTTTGTAGAATTTG | 51444 |
| rs756095815 | snp | A/C | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091435 | ATAAAATTAAAAAAA[A/C]CACTTAAATTAGTGA | 51444 |
| rs756211890 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123773 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTATCTGGT | 51444 |
| rs756258314 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100632 | AGGCATGCGCCACCA[G/T]GCCTGGCTAATTTTG | 51444 |
| rs756264063 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117502 | TTTGCATGCAACTGA[A/G]TAGAAAAAAAAATTG | 51444 |
| rs756277182 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102291 | ACTGCAAGCTCCACC[C/T]CCCAGGTTCACACCA | 51444 |
| rs756349926 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101690 | TGTCATGTTGCTTTC[C/T]CAAAAATTGAGCTAA | 51444 |
| rs756439289 | snp | A/C | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090524 | AATTATTATTATTCT[A/C]GGAATCAATGCTTTT | 51444 |
| rs756472992 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104762 | ATTGAAAAGTGTAAG[A/G]GAACATGACATTTAT | 51444 |
| rs756565626 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097725 | ATGAGGTTTCACTAT[A/G]TTGGCCAGGCTGGTC | 51444 |
| rs756570034 | in-del | -/GTGTGTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097970 | TGTGTGTGTGTGTGT[-/GTGTGTG]TTATTTTTGTTTGTT | 51444 |
| rs756613405 | snp | A/G | 1.72383e-05 | 0.00293578 | intron-variant | RNF138 | GRCh38.p7 | 18:32111957 | CTTCTTTGGAAGCCA[A/G]GTTTCTACTCTGAAA | 51444 |
| rs756631536 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126223 | CAACAGTGAGACTGT[A/G]TCTCTAGTTTTAAGA | 51444 |
| rs756634555 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125448 | TCCTAGAAGTGTTTC[A/T]TAGGTAAGTTATTTC | 51444 |
| rs756795483 | snp | A/G | 0.00220711 | 0.0331464 | intron-variant | RNF138 | GRCh38.p7 | 18:32123585 | ACAAGGTAAGCTTTT[A/G]AAAAATCCTGCCACT | 51444 |
| rs756802263 | snp | A/G | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091728 | AATAGTAAAGACTAA[A/G]TCTTGAACATTGACG | 51444 |
| rs756843916 | snp | C/T | 1.70828e-05 | 0.00292252 | intron-variant | RNF138 | GRCh38.p7 | 18:32124874 | TTTGAGACAGTCTTC[C/T]GCTTAGAATAAAACA | 51444 |
| rs756894238 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093579 | GTTCCCCTTTGTTTT[A/G]CCTTTCTGCTTACTT | 51444 |
| rs756963137 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106889 | ATTATTTGAAGTTTT[G/T]CCAGTAATCTCTCTG | 51444 |
| rs757036087 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116625 | GGCGTGAACATGGCT[C/T]ACTGTAGCCTTGACC | 51444 |
| rs757097074 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128597 | CTTAAAATCAGTTTA[C/G]TGTCAGATATTTGGC | 51444 |
| rs757246233 | snp | A/G | 0.000100993 | 0.00710537 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113843 | CTTTCAGATCTCTCA[A/G]GATTCAGTAGGGAAC | 51444 |
| rs757262354 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130364 | AATATAATGTGTGAC[C/T]GTGATATAGTGAGAA | 51444 |
| rs757401991 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127073 | TGATTTACATGAAAA[C/T]TCTGTCAAGATTTAA | 51444 |
| rs757403892 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104566 | CAAGAGAAACAATAA[G/T]AGTACAGGGAGGTTT | 51444 |
| rs757454160 | snp | C/T | | | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129142 | GCTAGATGAAGAAAC[C/T]CAATACCAAACTGCT | 51444 |
| rs757460398 | in-del | -/AAAG | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130570 | AACTAGAAGAACATA[-/AAAG]AAAGAGAATCTCAGA | 51444 |
| rs757495541 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090175 | TGCTTCAACCTGGAA[A/G]GCGCAGGTTGAAGTG | 51444 |
| rs757594679 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125660 | CTTCAGGACCGGGCA[C/T]GGTGGCTCATGCCTG | 51444 |
| rs757606067 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107832 | TATTTAATTATTTTT[-/A]TAACAGTTTTAATAT | 51444 |
| rs757749867 | snp | A/G | 3.27241e-05 | 0.00404487 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092853 | GTCAGGAGGTGCTCA[A/G]AACGCCCGTGCGGAC | 51444 |
| rs757772706 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113309 | GCAGTCCACCCATCC[C/T]AGCCTCCCAAAAGGC | 51444 |
| rs757801996 | in-del | -/CACGCACACACACG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115756 | TCTAAAACACACACA[-/CACGCACACACACG]CACGCACGCACACAC | 51444 |
| rs757842807 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130504 | AAAGGACTAAGAGTG[G/T]ATTTGCTGACATTCC | 51444 |
| rs758146452 | snp | C/T | 0.000199554 | 0.00998686 | intron-variant | RNF138 | GRCh38.p7 | 18:32123580 | AGAATACAAGGTAAG[C/T]TTTTGAAAAATCCTG | 51444 |
| rs758187433 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094867 | TGGGCCTCATTGTAG[-/T]TTTTTAGCACTCCCC | 51444 |
| rs758393408 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117531 | TGCAAAATAAATCCA[C/T]AGATCATTTCACTAA | 51444 |
| rs758407795 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113398 | TTTCTAACTCTGCCA[A/G]GCTGCAGAAGTTAAA | 51444 |
| rs758489833 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115213 | ACGCTTTTAATGACC[A/G]AATTTTCTTATCAGG | 51444 |
| rs758508871 | snp | C/G | 1.68562e-05 | 0.00290307 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111784 | TTTCCTGACTGCAAT[C/G]AGGGAAAGCGGAGCA | 51444 |
| rs758564342 | snp | C/T | 1.70269e-05 | 0.00291773 | intron-variant | RNF138 | GRCh38.p7 | 18:32111944 | ATGTGACATCTCTCT[C/T]CTTTGGAAGCCAAGT | 51444 |
| rs758752423 | in-del | -/GT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127277 | ACAAAGAGACTAAGA[-/GT]GTAAGAGAAGTTATA | 51444 |
| rs758909314 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099134 | AGTTTAAAGTTGAGA[A/G]AAATGTAAAGAGACC | 51444 |
| rs758940947 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107364 | CAGCTCAGGCAGTCC[A/G]CCCTCCTCGGCCTCC | 51444 |
| rs758984216 | snp | C/T | 0.000126095 | 0.00793926 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092712 | TAGGGAGTCGGGCCC[C/T]GGGCCGCCACCGTCA | 51444 |
| rs759020311 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114535 | TATGTGAGCTCCTGC[C/G]CATTTGAACCGTACA | 51444 |
| rs759041760 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126446 | TAGATGTGGTTTTTC[C/T]GTTGAAACATTTGTG | 51444 |
| rs759100364 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098336 | TTAAATTTTTTAGAG[A/C]TGGGGTCTTGCTTTG | 51444 |
| rs759212825 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113016 | GCTGGAAAACACACT[C/T]GAGAGATTCTGGCTA | 51444 |
| rs759254270 | snp | C/T | 0.000141313 | 0.00840455 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092695 | CCCCCTCCGGGTTCA[C/T]GTAGGGAGTCGGGCC | 51444 |
| rs759261116 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127956 | GTGTTGGCAGGTGCC[C/T]ATAGTCCCAGCTACT | 51444 |
| rs759332940 | in-del | -/TATGTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097943 | ATATGTGTATGTATA[-/TATGTG]TGTGTGTGTGTGTGT | 51444 |
| rs759378867 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121621 | AACAGTATTTTTAAA[G/T]GGCACATTCAAAACC | 51444 |
| rs759446683 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107981 | TGCCTTAGCCTCCTG[A/G]GTAGCTGGGATTACA | 51444 |
| rs759455302 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101552 | TGTAAAATGAAGGAA[-/C]TTATTAAGAAAAATT | 51444 |
| rs759513121 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124795 | AATTTTACCAGACAG[C/T]GTTTACTGGATCACT | 51444 |
| rs759516698 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117259 | GTTATATTCACGGTC[C/T]GAGCAGGAAACAGTG | 51444 |
| rs759598360 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101458 | GATTGGTCTTGAACT[C/G]CTGACCTCAAGTGAT | 51444 |
| rs759694854 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130125 | ATATGTGTGTATGCA[A/G]TTTGTCAGGTTATAT | 51444 |
| rs759713153 | snp | C/G/T | 0.000135883 | 0.00824175 | intron-variant | RNF138 | GRCh38.p7 | 18:32111940 | GTAAATGTGACATCT[C/G/T]TCTTCTTTGGAAGCC | 51444 |
| rs759768577 | in-del | -/GC | 0.000332945 | 0.0128981 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092649 | CCCGCCCCCTTCCTG[-/GC]GCGCGCTGTATCCTG | 51444 |
| rs759773658 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107127 | TTCCTTTTTTTTTTT[-/T]TTTTTTTTTTGGAGA | 51444 |
| rs759787235 | snp | C/T | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131683 | AAGAAAAAGCTACCA[C/T]ATGCTGGTGCTATAT | 51444 |
| rs759841100 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095432 | CTGTCTTGGCCTCCA[A/G]AAGTGCTGGGATGAC | 51444 |
| rs759855066 | in-del | -/CAAAGTTTAATACATCCAATATGTCAAGTTAAACCATTCTGGGATTTG | | | utr-variant-3-prime, cds-indel | RNF138 | GRCh38.p7 | 18:32130973 | TTTCATAGTTTCTTT[lengthTooLong]CAAAGTTTAATACAT | 51444 |
| rs759872887 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100468 | CCACACCCAACTAAC[-/T]TTTTTTTTTTTTTTT | 51444 |
| rs759986465 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094710 | AAAAAAATTTAAGTG[C/G]TGTGTTGGCATTGGG | 51444 |
| rs759998382 | snp | A/G | 1.66488e-05 | 0.00288515 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113801 | GAAGTATCAGGATGA[A/G]TATGGTGTTTCTTCT | 51444 |
| rs760243800 | in-del | -/TGTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097945 | ATGTGTATGTATATA[-/TGTG]TGTGTGTGTGTGTGT | 51444 |
| rs760288820 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130133 | GTATGCAGTTTGTCA[A/G]GTTATATATAGAATT | 51444 |
| rs760302830 | in-del | -/AA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121134 | GAGTGAGACTGTCTC[-/AA]AAAAAAACAAAACAA | 51444 |
| rs760514705 | in-del | -/TATGTATATA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097935 | GTGTGTGTATATGTG[-/TATGTATATA]TGTGTGTGTGTGTGT | 51444 |
| rs760555263 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122697 | GTCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCT | 51444 |
| rs760571921 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121135 | AGTGAGACTGTCTCA[-/A]AAAAAAACAAAACAA | 51444 |
| rs760605100 | in-del | -/TAA | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130706 | ATTTAATAAAAATGT[-/TAA]TAATTTTGGAAGTGC | 51444 |
| rs760651042 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094461 | AATGACATCTTGTTA[-/T]TTTGTGCAACAAATG | 51444 |
| rs760708251 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108337 | CTCTAAGGGAACATA[C/T]CCCACCTCCTTCAGG | 51444 |
| rs760713029 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104379 | TAGCAAATATACCTA[C/G]TTGTAAGCTTTAGGT | 51444 |
| rs760911207 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118543 | TTTCTCAAAAAATAA[C/T]AATAATGCCGGGCGC | 51444 |
| rs761099014 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127972 | ATAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 51444 |
| rs761132854 | snp | A/G | 1.76608e-05 | 0.00297155 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113755 | TACAGATTAAATTCT[A/G]TCGCATGAGACATCA | 51444 |
| rs761135655 | in-del | -/GTGTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097970 | TGTGTGTGTGTGTGT[-/GTGTG]TGTTATTTTTGTTTG | 51444 |
| rs761247202 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091052 | GGCTCACTGCAACCT[C/T]TGCCTCCCGGGTACA | 51444 |
| rs761336148 | snp | C/G | 0.000115807 | 0.00760855 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111869 | CGGGCCTTAGACCTT[C/G]AAAATATAATGAGGA | 51444 |
| rs761365641 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122838 | CAAAAACTAACTAAC[C/T]AACTAAATAAATAAA | 51444 |
| rs761567322 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119864 | TTGATAATCTAATTA[-/G]TTATTACTAGAGAGT | 51444 |
| rs761586972 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124616 | AATGAGAGAATCTTT[A/G]AATAGTCTAATAATT | 51444 |
| rs761678763 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111384 | TGGAGATCCAGTGTG[C/T]GTTAATTTGTTGGCC | 51444 |
| rs761703953 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109196 | TCTCACTCTGTTGCT[C/T]AGGCTGAAGTGCAGT | 51444 |
| rs761855028 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094764 | CAAGGTGAGAGGAAG[C/T]TGTAATAGCTGCTAA | 51444 |
| rs761860085 | snp | A/C | 0.00033687 | 0.0129739 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092683 | GCGATCCCCCTCCCC[A/C]CTCCGGGTTCATGTA | 51444 |
| rs761940423 | snp | C/T | 1.65504e-05 | 0.00287662 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124740 | GTTTTATAGTTCTTC[C/T]GGTCATCCTACTTTT | 51444 |
| rs762169665 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128427 | TCTGTAATCCTAGCT[A/T]CTTGGCAGGCTGAGG | 51444 |
| rs762245604 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115826 | TGATCTGGCCCTTTC[C/T]TCTCTTTTTATAGCC | 51444 |
| rs762337208 | in-del | -/TTTTTTTTTTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107117 | ACTTTCCTTTTTTCC[-/TTTTTTTTTTT]TTTTTTTTTTGGAGA | 51444 |
| rs762345556 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128142 | GCCTTGATTTTAAAG[C/T]GAAATGCATAGGGCA | 51444 |
| rs762391892 | snp | A/G | 3.068e-05 | 0.00391651 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092834 | GATTTCTACTGCCCC[A/G]TCTGTCAGGAGGTGC | 51444 |
| rs762433385 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114895 | AAAAACCTTTAGTGA[C/T]TGTCTGGTAAAGATC | 51444 |
| rs762514248 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112853 | TTTGAGTATATCCAT[A/G]TGTCTATAGATTTAT | 51444 |
| rs762517340 | in-del | -/TGTGTGTGTGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097967 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGT]TATTTTTGTTTGTTT | 51444 |
| rs762542279 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118547 | TCAAAAAATAATAAT[A/C]ATGCCGGGCGCAGTG | 51444 |
| rs762583777 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122071 | ACGGGGTTTCACCAT[C/G]TTGGCTAGGCTGATC | 51444 |
| rs762597705 | snp | C/T | 0.00012818 | 0.00800461 | intron-variant | RNF138 | GRCh38.p7 | 18:32092926 | GCGGAGCCGGGTTGT[C/T]GCTTAGGCCCGGCCT | 51444 |
| rs762794364 | snp | A/C | 1.69203e-05 | 0.00290859 | intron-variant | RNF138 | GRCh38.p7 | 18:32126816 | GTAAGTGAATTCTTC[A/C]AGATTAAGAAAGTAC | 51444 |
| rs762848884 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104349 | CCTCATTAAGGGTGG[C/T]TTCCCTAAAATCTAT | 51444 |
| rs762897213 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094547 | TGAGTGTTCACAGGC[A/G]TGTGTGAGATATGCC | 51444 |
| rs762925397 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129997 | AGAAACTTTCAGTTG[A/G]TGATATTGTATTCTA | 51444 |
| rs762967459 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110412 | TTAAGCATTTTATAC[A/T]TGTTATCTATTTTAA | 51444 |
| rs762996635 | snp | C/T | 1.64825e-05 | 0.00287071 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129192 | TAAACATCTGAAGGC[C/T]GTAGACATCTCTGCA | 51444 |
| rs763026509 | in-del | -/GAA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118170 | TGGCTAAATAGCTAT[-/GAA]GAAATCTGGCATAGT | 51444 |
| rs763044087 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106653 | CATGGCAAGCTCCGC[C/G]TCCCAGGTTCACGCC | 51444 |
| rs763261761 | snp | G/T | 1.67629e-05 | 0.00289503 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113834 | CATTCCAAACTTTCA[G/T]ATCTCTCAAGATTCA | 51444 |
| rs763263240 | in-del | -/TC | 5.03994e-05 | 0.00501968 | intron-variant | RNF138 | GRCh38.p7 | 18:32126679 | TTTTGTTTAAAACAA[-/TC]TGTTTCTTATAGACA | 51444 |
| rs763299755 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116162 | ATGTTAGTTCTTCCT[C/T]ATCATCCTCATTATC | 51444 |
| rs763307569 | snp | C/T | 3.35464e-05 | 0.00409537 | intron-variant | RNF138 | GRCh38.p7 | 18:32123495 | ACTTTGAGGTATTAA[C/T]TTTTTCCCCTGTGCT | 51444 |
| rs763354919 | in-del | -/AG | 2.79302e-05 | 0.00373689 | intron-variant | RNF138 | GRCh38.p7 | 18:32111707 | TAATTATAGAGATGA[-/AG]AGAGTAATTTTTTTT | 51444 |
| rs763384869 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096474 | TGGAGCTAAAGCTGT[A/G]GGTGTCGAAGTGGTC | 51444 |
| rs763447189 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131302 | GATTGTTTAAAATTT[A/C]CCCTCTTTTTGTCAG | 51444 |
| rs763527753 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121978 | GTTTCAAGCGATTCT[A/C]ATGCCTCAGCCTCCC | 51444 |
| rs763535394 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117192 | CAGGCATGAACCACC[C/T]GCGCCCAGCCAGAAA | 51444 |
| rs763574627 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118553 | AATAATAATAATGCC[A/G]GGCGCAGTGGCTCAC | 51444 |
| rs763600563 | snp | A/G | 3.09938e-05 | 0.00393649 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092842 | CTGCCCCGTCTGTCA[A/G]GAGGTGCTCAAAACG | 51444 |
| rs763654098 | snp | A/G | 5.47011e-05 | 0.00522949 | intron-variant | RNF138 | GRCh38.p7 | 18:32092931 | GCCGGGTTGTCGCTT[A/G]GGCCCGGCCTCCGGC | 51444 |
| rs763728867 | snp | A/C | 1.6669e-05 | 0.00288691 | intron-variant | RNF138 | GRCh38.p7 | 18:32124849 | ATAGTTCCTGTGGTA[A/C]GTACATACGTTTGAG | 51444 |
| rs763759065 | in-del | -/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097977 | TGTGTGTGTGTGTGT[-/G]TATTTTTGTTTGTTT | 51444 |
| rs763901615 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130221 | TGTTTAAAATTTTGT[A/C]TATCACCAAATTTTT | 51444 |
| rs763974419 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094679 | CTAGCATAACTTGGT[C/T]CCTTTCCAATATTTA | 51444 |
| rs764053446 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122714 | CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAGGC | 51444 |
| rs764136681 | snp | A/G | 1.67626e-05 | 0.002895 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113835 | ATTCCAAACTTTCAG[A/G]TCTCTCAAGATTCAG | 51444 |
| rs764141412 | in-del | -/AAT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118845 | AAAAAAAAAGAAAAT[-/AAT]AATAATAATAATAAT | 51444 |
| rs764228301 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090117 | TTGGCATGGTGGTGC[A/G]TGCCTGTAATCTCAG | 51444 |
| rs764347827 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104409 | TGCTTTTCTAGTTAG[A/G]AACTAGTCAAAGAAG | 51444 |
| rs764461536 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091071 | CTCCCGGGTACAAGC[A/G]ATTCTCGTGCCTCAG | 51444 |
| rs764524736 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114777 | TATTTTAGTAGCCTT[C/T]CATTTTACATATTGC | 51444 |
| rs764669071 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126957 | ACTGGTGAACTTTAG[C/T]TTGTAGAAATGGTAA | 51444 |
| rs764756812 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127980 | AGCTACTCGGGAGGC[A/T]GAGGCAGGAGAATGG | 51444 |
| rs764761557 | snp | A/G | 3.72141e-05 | 0.00431343 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092808 | CTGCGGCCACGTCCT[A/G]CACCGAAGATGATTT | 51444 |
| rs764856312 | snp | C/T | 4.17894e-05 | 0.00457088 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092697 | CCCTCCGGGTTCATG[C/T]AGGGAGTCGGGCCCC | 51444 |
| rs764884331 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105258 | ACCATACATGGCTAA[-/T]TTTTTGTATTTTTAG | 51444 |
| rs764928367 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122892 | GTAGCACACAGGTGA[C/T]GGTCCCTGTATGGAA | 51444 |
| rs765016361 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF138 | GRCh38.p7 | 18:32092550 | CCATCCAGCCCCCTG[C/T]GGGAGGAGCCGTGGG | 51444 |
| rs765031569 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117506 | CATGCAACTGAGTAG[A/G]AAAAAAAATTGCAAA | 51444 |
| rs765068436 | snp | C/G/T | 3.32415e-05 | 0.00407675 | intron-variant | RNF138 | GRCh38.p7 | 18:32123579 | GAGAATACAAGGTAA[C/G/T]CTTTTGAAAAATCCT | 51444 |
| rs765113659 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103993 | AAAACTTCATAGCAA[A/T]TTAGGAATAGGCTAA | 51444 |
| rs765115962 | in-del | -/CT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111585 | CAGTTATCAGTCTTA[-/CT]CTCTGATAAATACAT | 51444 |
| rs765181511 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111437 | GGCAGAGCCAGGATC[C/T]GGTTTTTCCTTTGTA | 51444 |
| rs765227185 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094813 | AGCAGGTCTTTTTTG[C/G]ATAGAATCATTCTAA | 51444 |
| rs765269363 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095751 | TAAAATATAAACTCC[C/T]GTTTAATCCCCATTC | 51444 |
| rs765285428 | in-del | -/GTGTT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097974 | TGTGTGTGTGTGTGT[-/GTGTT]ATTTTTGTTTGTTTG | 51444 |
| rs765342723 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110202 | CTTGCTATGTTGCCC[A/G]GGCTGGTCTTCAACT | 51444 |
| rs765379880 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128164 | CATAGGGCATAAAAT[C/T]GATAGCAAATATAAT | 51444 |
| rs765414152 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107267 | CTGGGACTACAGGTG[C/G]ACGCTGCCACGCCCA | 51444 |
| rs765445823 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127194 | AAATCTTAGATTTCT[C/G]AAATCTAGCATGTAA | 51444 |
| rs765520394 | in-del | -/CCCCCTC | 0.000411777 | 0.0143429 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092672 | GTATCCTGATGCGAT[-/CCCCCTC]CCCCCTCCCCCCTCC | 51444 |
| rs765583844 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107032 | GAAAATAATTTTCTC[-/TT]TCTGTCTCCTATGGC | 51444 |
| rs765639286 | snp | C/T | 1.66477e-05 | 0.00288506 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113804 | GTATCAGGATGAATA[C/T]GGTGTTTCTTCTATC | 51444 |
| rs765643515 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094783 | AATAGCTGCTAACTA[C/T]ATATATATATATAAA | 51444 |
| rs765808934 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115034 | TTTTAGTCCTTCTGG[G/T]TTTCTTCATTTCTAT | 51444 |
| rs765814312 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095845 | CTCTGGAGACTTAAT[A/G]GTCCGCTGGAGAGAC | 51444 |
| rs765816349 | in-del | -/TG | 0.000161052 | 0.00897219 | intron-variant | RNF138 | GRCh38.p7 | 18:32111968 | GCCAAGTTTCTACTC[-/TG]AAATTCTTATTTGAA | 51444 |
| rs765848334 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130323 | ACACAATTACCTGTT[G/T]ATATGGTGCTCATTT | 51444 |
| rs765904532 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099104 | TGCGTAATGGAAATT[C/T]GTCTAGCATCTGCTA | 51444 |
| rs765981080 | snp | A/G | 5.18614e-05 | 0.00509195 | intron-variant | RNF138 | GRCh38.p7 | 18:32124885 | CTTCTGCTTAGAATA[A/G]AACATGCTGTTCTAT | 51444 |
| rs766098626 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120384 | CATTGTGCTTACTAT[G/T]TAACATTGGATAGAG | 51444 |
| rs766132886 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112636 | GCGGTGAGCTGAGAT[C/T]GCGCCATTGCACTCC | 51444 |
| rs766210017 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104593 | GTTTGATGCAAGAAC[A/C]GACAAAAATCAACAA | 51444 |
| rs766221578 | snp | A/C/T | 3.19551e-05 | 0.00399709 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092694 | CCCCCCTCCGGGTTC[A/C/T]TGTAGGGAGTCGGGC | 51444 |
| rs766316140 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125066 | GATGCATAGTGTGAG[C/G]TAATATAGCACAGTC | 51444 |
| rs766381366 | in-del | -/AAA | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091441 | TTAAAAAAAACACTT[-/AAA]TTAGTGAATAACCTT | 51444 |
| rs766540534 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107050 | CTGTCTCCTATGGCT[A/G]CTGGGCCACTGGATT | 51444 |
| rs766687853 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130067 | AAATTTATTCAAAGC[C/T]AAAGATGTATATATA | 51444 |
| rs766714253 | snp | C/T | 1.65581e-05 | 0.00287728 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111887 | AATATAATGAGGAAG[C/T]TTTCTGGTAGCTGCA | 51444 |
| rs766955465 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099984 | TAGTGAAGTGTCTTG[G/T]TCATGGAAAGTGCTC | 51444 |
| rs766960918 | snp | A/T | 3.30863e-05 | 0.00406719 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111872 | GCCTTAGACCTTGAA[A/T]ATATAATGAGGAAGT | 51444 |
| rs767047128 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101372 | TACAGGCGTGCACCA[C/T]CACTCCTGGCTAATT | 51444 |
| rs767356050 | snp | A/G | 1.64947e-05 | 0.00287177 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129219 | TGCATCTTTGTACCT[A/G]CAAGTGCCATCTTTA | 51444 |
| rs767419586 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32108107 | TGATCCACCCGCCTC[A/G]GCTCCTCAAGGTGCT | 51444 |
| rs767432821 | snp | A/G | 1.65364e-05 | 0.0028754 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32123530 | AAGCAATAGGAGTGA[A/G]ACATCCACATCTGAT | 51444 |
| rs767617568 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121622 | ACAGTATTTTTAAAG[C/G]GCACATTCAAAACCC | 51444 |
| rs767697984 | snp | C/T | 1.64969e-05 | 0.00287196 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124782 | GTGTCAAGAATCAAA[C/T]TTTACCAGACAGCGT | 51444 |
| rs767698837 | snp | A/G | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131697 | ACATGCTGGTGCTAT[A/G]TGTCAGATTTAACTT | 51444 |
| rs767698973 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116450 | CGGAGTTCTGATTGC[A/C]ATGGAAGAATTGAGT | 51444 |
| rs767788557 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117313 | AGAATTTAGTAAAGA[G/T]ACTATTTTCAAAGAG | 51444 |
| rs767885983 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102019 | GTAGCTGGGACTACA[A/G]GCGTGCACCACCATG | 51444 |
| rs767941495 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126558 | GAAATGATCTAGTCA[C/T]GGAACTTGGCCTTTA | 51444 |
| rs767972821 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125148 | TAGCACAACCTGTCT[A/G]TTGAGGCCTCAGTTA | 51444 |
| rs767999453 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101369 | GATTACAGGCGTGCA[C/T]CACCACTCCTGGCTA | 51444 |
| rs768113844 | in-del | -/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097941 | GTATATGTGTATGTA[-/TA]TATGTGTGTGTGTGT | 51444 |
| rs768267760 | snp | A/G | 1.66804e-05 | 0.00288789 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111801 | GGGAAAGCGGAGCAC[A/G]TTGTCCCCTATGTCG | 51444 |
| rs768380742 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130931 | TAAGACTTTTGACCA[C/T]AGTGTTTTCCAGTTT | 51444 |
| rs768392287 | snp | C/T | 2.9363e-05 | 0.00383153 | intron-variant | RNF138 | GRCh38.p7 | 18:32113711 | TCTTACGAGTTCTAT[C/T]TTAAATTAAAAGTCA | 51444 |
| rs768526745 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124335 | TTAGAAGTTTTAAGT[G/T]CCTAGATAAAAGGTT | 51444 |
| rs768622714 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121224 | ATCCTGGCCAGGTGT[C/G]GTGGCTCATGCTTGT | 51444 |
| rs768711232 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106740 | TAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACA | 51444 |
| rs768736694 | snp | A/C/G | 0.000171388 | 0.00925578 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092784 | CCCCCGCCATGGCCG[A/C/G]GGACCTCTCTGCGGC | 51444 |
| rs768835081 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099244 | GATTTGTACCTTTTT[C/T]CTTCCTACTTCTGCT | 51444 |
| rs768867737 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098126 | CAAGTAGTTGGGATT[A/G]CAGGCGTGCACCATC | 51444 |
| rs768979885 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119916 | TTGTTTTCAGCAGCT[C/T]TGATGATTTGTTAGT | 51444 |
| rs769103988 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107646 | CTACCTCAGCCTCCC[A/T]AGTAGCTAGGATTAC | 51444 |
| rs769135148 | snp | C/G | 3.30327e-05 | 0.0040639 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126710 | ATGTCCTATTTGTGT[C/G]TCTCTTCCTTGGGGA | 51444 |
| rs769148779 | snp | C/T | | | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129121 | TTATTGTTTTTAGAA[C/T]CTTCAGCTAGATGAA | 51444 |
| rs769189887 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109364 | GGCTGGTCTTGTGAG[C/T]TTAAGCCATTTGCCC | 51444 |
| rs769192375 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100919 | CTGAGATATATTTAA[A/G]TTAAAATAAATGCTC | 51444 |
| rs769289416 | in-del | -/TGTGTATATATATA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101390 | CTCCTGGCTAATTTT[-/TGTGTATATATATA]TATTTTTAAATTAGA | 51444 |
| rs769479251 | snp | C/T | 1.67492e-05 | 0.00289384 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111793 | TGCAATGAGGGAAAG[C/T]GGAGCACATTGTCCC | 51444 |
| rs769520396 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117687 | CATCTAAAATAATCT[G/T]TGTCACTTTCATTCA | 51444 |
| rs769582697 | snp | A/G | 1.74772e-05 | 0.00295606 | intron-variant | RNF138 | GRCh38.p7 | 18:32092919 | CCCCCTCGCGGAGCC[A/G]GGTTGTCGCTTAGGC | 51444 |
| rs769623917 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114181 | TGATTTGAAAAACTA[C/T]AGAAAATCCTTTTCA | 51444 |
| rs769679404 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125914 | AAATACAGTGCCAAA[A/G]ATGTTCCAGGAAATC | 51444 |
| rs769754344 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109626 | GGCACCATGGCTCAC[G/T]CCTGTAATCCCAACA | 51444 |
| rs769826631 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130721 | TTAATTTTGGAAGTG[C/T]AGTTTTGTAAAAACC | 51444 |
| rs769886830 | snp | A/C | 8.81795e-05 | 0.00663943 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092763 | GCCATCGCCTTGTTT[A/C]CCCATCCCCCGCCAT | 51444 |
| rs769951469 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100732 | CCACCCACCTCGGCC[G/T]ACCAAAGTGTTGGGA | 51444 |
| rs769956858 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122563 | GCGCGGTGGCTCACA[A/C]CTGTAATCGCAGCAG | 51444 |
| rs769993063 | in-del | -/TC | 1.78745e-05 | 0.00298947 | intron-variant | RNF138 | GRCh38.p7 | 18:32124896 | AATAAAACATGCTGT[-/TC]TATTTATTTCACTTC | 51444 |
| rs770015221 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121451 | GGTGAGCCGCGGTCG[C/T]GCCACTGCATTCCAG | 51444 |
| rs770100839 | in-del | -/A | 5.64748e-05 | 0.00531359 | intron-variant | RNF138 | GRCh38.p7 | 18:32113719 | GTTCTATTTTAAATT[-/A]AAAGTCACATTTTAA | 51444 |
| rs770107018 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107940 | GCTCACTGCAAGCTC[C/T]ACCTCCCAGGTACGA | 51444 |
| rs770213176 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126585 | TTAAAAATGCTTCTC[-/A]ACGTAGATATTTTTG | 51444 |
| rs770232761 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094317 | GATACCAACTCTTCT[C/T]ATTTTTTCCCCAATC | 51444 |
| rs770285622 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117009 | CAGGTTCAAGTGATT[C/T]TCCTGCCTAAGCCTC | 51444 |
| rs770294613 | snp | A/C | 5.97627e-05 | 0.00546606 | intron-variant | RNF138 | GRCh38.p7 | 18:32113904 | ATTTTCATAATTGAA[A/C]TGGAAATTGTTTTGG | 51444 |
| rs770312780 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095050 | AGTTCTGCCTGAACA[A/G]TGAATTAAAAGAATA | 51444 |
| rs770389519 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131138 | TCTTTAAAGGAAAAT[C/T]GTAGTAGAGGTCATC | 51444 |
| rs770401825 | snp | A/C | 0.000167974 | 0.0091629 | intron-variant | RNF138 | GRCh38.p7 | 18:32123605 | ATCCTGCCACTTTAG[A/C]AAGTAATATTATATT | 51444 |
| rs770411909 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130271 | GCTAAGTTATCTAGT[C/T]GGCTACTATTACACC | 51444 |
| rs770416244 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095938 | ATTAGCCTAAAGGAT[A/G]GGGATAATTTCCTAG | 51444 |
| rs770563806 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103699 | CCGGGTGTGGTGGCT[C/T]ACGCCTGTAATCCCA | 51444 |
| rs770623501 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126350 | TATGGTTATTGTATG[A/G]ATCAAATGAGATAAT | 51444 |
| rs770649845 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113658 | TAAATGGAGTATTTA[C/G]TTACTTTTATTTTTT | 51444 |
| rs770733419 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090815 | CCTTAAATGGCTTCT[A/G]TTTATTCATTTAGAC | 51444 |
| rs770742698 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099327 | AGATGAGAATAATTC[A/G]TTTTATGTCTGAAGA | 51444 |
| rs770801382 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114495 | CCAGGTCAAGAAAGA[A/T]CATTTTTCAAAACTT | 51444 |
| rs770899123 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115676 | CTTGACCCTAGGAAA[C/T]GGAGGTTGCAGTGAG | 51444 |
| rs770899609 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095309 | CAAGTTGCTGGGACT[A/G]CAGGAGCATGCCTCC | 51444 |
| rs770913259 | snp | C/G | 9.72053e-05 | 0.00697088 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092793 | TGGCCGAGGACCTCT[C/G]TGCGGCCACGTCCTA | 51444 |
| rs770926306 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131319 | CCTCTTTTTGTCAGT[G/T]CATTGGGAATAGGGA | 51444 |
| rs770986146 | in-del | -/A | 1.66639e-05 | 0.00288646 | intron-variant | RNF138 | GRCh38.p7 | 18:32123584 | ACAAGGTAAGCTTTT[-/A]GAAAAATCCTGCCAC | 51444 |
| rs771064744 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129164 | CAAACTGCTGTTGAA[C/G]AATCTTTTCAAGTAA | 51444 |
| rs771244622 | snp | G/T | 0.000115477 | 0.0075977 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092651 | CGCCCCCTTCCTGGC[G/T]CGCGCTGTATCCTGA | 51444 |
| rs771435681 | snp | A/G | 6.94179e-05 | 0.00589102 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113758 | AGATTAAATTCTATC[A/G]CATGAGACATCATTA | 51444 |
| rs771521624 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117953 | ATACAGAAGACATTT[C/T]AATTTTATCCTCCTT | 51444 |
| rs771588541 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127871 | GGATCACAAGGTCAG[C/G]AGATTGAGACCATCC | 51444 |
| rs771609381 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115758 | TAAAACACACACACA[C/T]GCACACACACGCACG | 51444 |
| rs771639268 | snp | C/G/T | 5.37036e-05 | 0.00518164 | missense, synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113753 | TTTACAGATTAAATT[C/G/T]TATCGCATGAGACAT | 51444 |
| rs771671458 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091193 | GGCTGGTCTTGAACT[C/G]CTGACCTCAAGTGAT | 51444 |
| rs771680052 | in-del | -/AA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127051 | AGCACCCAGATTAAC[-/AA]AATGATGATTTACAT | 51444 |
| rs771694161 | snp | C/G | 3.64977e-05 | 0.00427171 | intron-variant | RNF138 | GRCh38.p7 | 18:32113877 | TAAGCAATACTTATT[C/G]CTAAATACAGAATTT | 51444 |
| rs771733408 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101232 | TTTTTTTTTTTTTTC[A/G]AAGACAGAGTCTGGC | 51444 |
| rs771735030 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129624 | TATTAGAGTTGCAGA[A/C]TAGAAACTTGAAGTG | 51444 |
| rs771750091 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123652 | CTTTTTAAATTAAAC[-/T]TTTTTTTTTTTTTTT | 51444 |
| rs771849961 | in-del | -/TGTGTAATGTGTGTCAAGA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32129006 | TAACTGTCCTGAGTG[-/TGTGTAATGTGTGTCAAGA]TGTGTAATGTGTATC | 51444 |
| rs771872055 | in-del | -/TTC | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090975 | TTTATCCTTTTTTTG[-/TTC]TTCTTTTTTTTTGAG | 51444 |
| rs771872858 | snp | C/T | 0.000165906 | 0.00910635 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092684 | CGATCCCCCTCCCCC[C/T]TCCGGGTTCATGTAG | 51444 |
| rs771897331 | in-del | -/AAG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111517 | ATCATATATTATGTT[-/AAG]AAGTTGTAAAGCAGA | 51444 |
| rs771937603 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099453 | TGTTGCCCAGACTGG[A/G]GTGCAGTGGTGCAGT | 51444 |
| rs771987151 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116995 | CAACATCGACCTCCC[A/G]GGTTCAAGTGATTCT | 51444 |
| rs772000318 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122668 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGCCGGT | 51444 |
| rs772146232 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118447 | GCTGAGGCAGGAGAA[C/T]TTCTTGAACCCAGGA | 51444 |
| rs772156770 | snp | C/T | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126755 | TACCAGAAATTTCGT[C/T]AGTCATCTAAATCAG | 51444 |
| rs772370941 | snp | A/T | 1.6489e-05 | 0.00287128 | intron-variant | RNF138 | GRCh38.p7 | 18:32129116 | GAATGTTATTGTTTT[A/T]AGAATCTTCAGCTAG | 51444 |
| rs772471390 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091020 | TCGCCAGGGCTGGAG[A/T]GCAGCGGCGCGATCG | 51444 |
| rs772521122 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119714 | CAGGAGTGAGCCACT[A/G]CCCCCAGCCTCTTTC | 51444 |
| rs772660133 | snp | C/T | | | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124787 | AAGAATCAAATTTTA[C/T]CAGACAGCGTTTACT | 51444 |
| rs772673779 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105844 | TTATATCAGAACAGA[C/T]AGCTTTCTATGTGAC | 51444 |
| rs772726576 | in-del | -/TGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097967 | GTGTGTGTGTGTGTG[-/TGT]GTGTGTGTTATTTTT | 51444 |
| rs772811173 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101279 | GAGTGCAGTGGCACA[C/T]GCAGTCTTGGCTCAC | 51444 |
| rs772899001 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107029 | TTTGAAAATAATTTT[-/C]TCTTTCTGTCTCCTA | 51444 |
| rs772943061 | in-del | -/AAAAT | | | upstream-variant-2KB | RNF138 | GRCh38.p7 | 18:32091402 | GAGTACCTGTCTCAA[-/AAAAT]AAAATAAAATAAAAT | 51444 |
| rs772980589 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102965 | AAATAGTTTTGTGAT[C/G]TAAATTGATTTTTTG | 51444 |
| rs772996006 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096883 | CTACAGGCACTCACC[A/G]CCATGCCTGGCTATT | 51444 |
| rs773165490 | snp | C/T | 4.62043e-05 | 0.00480625 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092685 | GATCCCCCTCCCCCC[C/T]CCGGGTTCATGTAGG | 51444 |
| rs773256101 | snp | C/T | 3.29968e-05 | 0.00406169 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32124788 | AGAATCAAATTTTAC[C/T]AGACAGCGTTTACTG | 51444 |
| rs773272663 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109743 | AGTACAAAAATTAGC[C/T]GTCGCAGTGGTGCAT | 51444 |
| rs773317592 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112000 | TTTTCTTGGTTGGTG[-/T]TTTTTTTTTTTTTGA | 51444 |
| rs773327715 | snp | A/C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117153 | GTGATCCACCTGCCT[A/C/T]GGCCTCCCAAAGTGA | 51444 |
| rs773366597 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094385 | GTTGTGTGAGCCAAG[A/T]GTGTGTGGATTTTCA | 51444 |
| rs773379320 | snp | A/G | 1.65299e-05 | 0.00287483 | synonymous-codon, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126779 | AAATCAGAGACATCA[A/G]TTTGATTATGGAGAA | 51444 |
| rs773390709 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129925 | TGAATAACAGCTCTT[C/T]GGCCTCAGAATTTTC | 51444 |
| rs773405492 | in-del | -/C | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131922 | ATACAATGTCATATA[-/C]CTTGTATGGGTTGCT | 51444 |
| rs773551501 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122598 | GGAGGCTGAGGTGGG[C/T]GGATCACTTGAGCTC | 51444 |
| rs773680443 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127734 | TGGAAATACAAAAAT[A/T]TGTGAACCACTTTTG | 51444 |
| rs773688913 | in-del | -/TTTTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106538 | AGTTGAAAAATTATT[-/TTTTA]TTTTATTTTATTTAT | 51444 |
| rs773745762 | snp | A/C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101331 | TCAAGCCATTCTTCT[A/C/G]CCTCAGTCTTCTGAG | 51444 |
| rs773830705 | snp | C/G | 3.67755e-05 | 0.00428794 | intron-variant | RNF138 | GRCh38.p7 | 18:32092934 | GGGTTGTCGCTTAGG[C/G]CCGGCCTCCGGCCCG | 51444 |
| rs773879498 | in-del | -/ATGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097944 | TATGTGTATGTATAT[-/ATGT]GTGTGTGTGTGTGTG | 51444 |
| rs773886014 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097430 | AGCTTGAACATCCAG[G/T]TCCTGAGTTTTTAGT | 51444 |
| rs773953604 | snp | A/G | 1.65647e-05 | 0.00287786 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111835 | AAATGTGACTAGAAG[A/G]GAGAGAGCATGTCCT | 51444 |
| rs774007997 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126969 | TAGCTTGTAGAAATG[A/G]TAAGGTAAAAATTGA | 51444 |
| rs774112758 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090880 | AACCTTTCTTTTCTC[G/T]GAAGCTAATTGTAGA | 51444 |
| rs774153957 | in-del | -/ATAG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100156 | TATTGTAAAGAGCAA[-/ATAG]ATAGGATCCCTGCCC | 51444 |
| rs774296897 | snp | C/G/T | 4.94518e-05 | 0.00497231 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129198 | TCTGAAGGCTGTAGA[C/G/T]ATCTCTGCATCTTTG | 51444 |
| rs774325915 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121482 | CCGGGGCAATAAGAG[C/T]GAAACTCCATCTCAA | 51444 |
| rs774363696 | snp | G/T | | | downstream-variant-500B | RNF138 | GRCh38.p7 | 18:32131575 | TACTTGTGTGTCTAA[G/T]TAAAATTTGTCTGGA | 51444 |
| rs774509376 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32103229 | AACTCTGTTGCCCAG[A/G]CTGGAGTACAGTGGG | 51444 |
| rs774525548 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117255 | CTGTGTTATATTCAC[A/G]GTCTGAGCAGGAAAC | 51444 |
| rs774637962 | snp | A/G | 1.71557e-05 | 0.00292875 | intron-variant | RNF138 | GRCh38.p7 | 18:32124701 | TTTGTGTTATTCTGA[A/G]TTAAGTATGTTTCAC | 51444 |
| rs774700898 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095374 | ACAGGGCCTCACTAC[A/G]TTGCCCAGTCAGATC | 51444 |
| rs774705010 | in-del | -/ATTATT | | | upstream-variant-2KB, cds-indel | RNF138, RNF125 | GRCh38.p7 | 18:32090510 | CTATTCATTGGACAA[-/ATTATT]ATTATTCTAGGAATC | 51444 |
| rs774711716 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118022 | TCTTGACTCTGTAAA[C/T]GTTAGTAACTGGATG | 51444 |
| rs774797638 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115761 | AACACACACACACGC[A/G]CACACACGCACGCAC | 51444 |
| rs774799012 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105711 | AAAAGCATAAACCAT[A/G]ATTTTAGGAAAAGGC | 51444 |
| rs774858657 | in-del | -/A | 1.67449e-05 | 0.00289347 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129214 | TCTCTGCATCTTTGT[-/A]ACCTGCAAGTGCCAT | 51444 |
| rs774993783 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128979 | AAAAGATACTGTTAT[A/G]TATGTTTTACATAAC | 51444 |
| rs775001140 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099518 | AGAGATTCTCCTGCC[C/T]CAATCTCCCGTGTAG | 51444 |
| rs775018231 | snp | G/T | 1.7532e-05 | 0.00296069 | intron-variant | RNF138 | GRCh38.p7 | 18:32092920 | CCCCTCGCGGAGCCG[G/T]GTTGTCGCTTAGGCC | 51444 |
| rs775197762 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114681 | AGTAGTAAGCACATA[C/T]GTAACTGTAAGGAAA | 51444 |
| rs775349440 | snp | A/G | 3.34762e-05 | 0.00409108 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111794 | GCAATGAGGGAAAGC[A/G]GAGCACATTGTCCCC | 51444 |
| rs775371191 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32122686 | AAAATTAGCCGGTCA[C/T]GGTGGCTCACGCCTG | 51444 |
| rs775419697 | snp | A/C | 0.000182999 | 0.0095638 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092679 | TGATGCGATCCCCCT[A/C]CCCCCTCCGGGTTCA | 51444 |
| rs775459146 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110205 | GCTATGTTGCCCAGG[C/T]TGGTCTTCAACTCCT | 51444 |
| rs775461793 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104232 | TGGCCAGGTTGGTCT[A/C]GAACTCCTGAGGTCA | 51444 |
| rs775491996 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118457 | GAGAATTTCTTGAAC[C/G]CAGGAGGCAGAGGTT | 51444 |
| rs775513329 | in-del | -/TTTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107515 | TAATTTAGTTTTTTG[-/TTTG]TTTGTTTGTTTGTTT | 51444 |
| rs775567400 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121744 | GTGACACATGCTGTT[C/T]TTGGTAACAAAATCA | 51444 |
| rs775632816 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105987 | GCCCAACATTCATTC[-/A]TTCTTAGTTCAGTTT | 51444 |
| rs775706792 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114153 | TTTTCTCTTACTGAT[C/T]TTGCAACTGAAATGA | 51444 |
| rs775727373 | in-del | -/T | 1.83576e-05 | 0.00302959 | intron-variant | RNF138 | GRCh38.p7 | 18:32126661 | TCATTGTTTTTATTA[-/T]TTTTTTGTTTAAAAC | 51444 |
| rs775760770 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32123835 | TTTTTGTATTTTTAG[G/T]AGAAACAGGGTTTCA | 51444 |
| rs775785039 | in-del | -/A | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118102 | AAAAAAATTACCAGC[-/A]AGTCTTTTATTTTTC | 51444 |
| rs775829494 | in-del | -/T | 3.34599e-05 | 0.00409009 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092760 | GTCGCCATCGCCTTG[-/T]TTCCCCATCCCCCGC | 51444 |
| rs775926455 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091037 | CAGCGGCGCGATCGC[A/G]GCTCACTGCAACCTC | 51444 |
| rs775938506 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100962 | TAATTACAAATGTAT[A/C]GGTTTCGAGAGAGTA | 51444 |
| rs775982301 | snp | A/G | 1.67778e-05 | 0.00289631 | intron-variant | RNF138 | GRCh38.p7 | 18:32123493 | TTACTTTGAGGTATT[A/G]ACTTTTTCCCCTGTG | 51444 |
| rs775987995 | in-del | -/TAT | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130277 | TATCTAGTTGGCTAC[-/TAT]TATTACACCTTAAAA | 51444 |
| rs776033441 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096043 | ATGAATGTGAGCTGG[A/T]CTTTGAAGTTTGGCT | 51444 |
| rs776102578 | snp | C/T | 1.68496e-05 | 0.0029025 | intron-variant | RNF138 | GRCh38.p7 | 18:32123614 | CTTTAGCAAGTAATA[C/T]TATATTTATCACTTA | 51444 |
| rs776239716 | in-del | -/TTTG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097982 | TGTGTGTGTGTTATT[-/TTTG]TTTGTTTGTTTGTTT | 51444 |
| rs776240160 | in-del | -/TTA | | | utr-variant-3-prime, cds-indel, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129605 | ACAAATCTGAGCCAG[-/TTA]TTATTAGAGTTGCAG | 51444 |
| rs776321463 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112623 | GGCGGCAGAGGTTGC[A/G]GTGAGCTGAGATTGC | 51444 |
| rs776421560 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111278 | CTTTTGTAGTAGACC[C/T]GTTTATGTCTTGTGG | 51444 |
| rs776458342 | snp | C/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116586 | AGACAGGGTCTTGCT[C/G]TGTCATCCAGCCTGG | 51444 |
| rs776550133 | snp | G/T | 1.65094e-05 | 0.00287305 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092798 | GAGGACCTCTCTGCG[G/T]CCACGTCCTACACCG | 51444 |
| rs776579486 | in-del | -/T | 1.67494e-05 | 0.00289386 | intron-variant | RNF138 | GRCh38.p7 | 18:32123600 | GAAAAATCCTGCCAC[-/T]TTAGCAAGTAATATT | 51444 |
| rs776604820 | snp | C/T | 1.69289e-05 | 0.00290933 | intron-variant | RNF138 | GRCh38.p7 | 18:32092902 | GTGAGTAGACGCCCC[C/T]TCCCCCTCGCGGAGC | 51444 |
| rs776633388 | in-del | -/TATA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097939 | GTGTATATGTGTATG[-/TATA]TATGTGTGTGTGTGT | 51444 |
| rs776679074 | snp | A/G | 1.64808e-05 | 0.00287057 | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129189 | AAGTAAACATCTGAA[A/G]GCTGTAGACATCTCT | 51444 |
| rs776712622 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32120304 | AAATTAAAAACATAT[A/G]TACATCTGGCTAGAG | 51444 |
| rs776724322 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107831 | TTATTTAATTATTTT[C/T]ATAACAGTTTTAATA | 51444 |
| rs776726002 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091077 | GGTACAAGCGATTCT[C/T]GTGCCTCAGCCTCCC | 51444 |
| rs776785775 | in-del | -/TGTGT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097971 | GTGTGTGTGTGTGTG[-/TGTGT]GTTATTTTTGTTTGT | 51444 |
| rs776945265 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130110 | TGTGTATATATACAC[-/AT]ATGTGTGTATGCAGT | 51444 |
| rs776959973 | snp | A/G | 1.70162e-05 | 0.00291682 | synonymous-codon, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113765 | ATTCTATCGCATGAG[A/G]CATCATTACAAATCT | 51444 |
| rs777085414 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129378 | TAAAAAATGAAAGTT[A/G]TGACATTAGCTTTAA | 51444 |
| rs777181552 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117344 | TAGTATGTTAGGTAC[A/G]CTATATAAGTAGGGT | 51444 |
| rs777185087 | snp | C/T | 3.7255e-05 | 0.0043158 | intron-variant | RNF138 | GRCh38.p7 | 18:32113885 | ACTTATTCCTAAATA[C/T]AGAATTTTCATAATT | 51444 |
| rs777208385 | snp | A/G | 1.68635e-05 | 0.0029037 | intron-variant | RNF138 | GRCh38.p7 | 18:32123467 | GATAATGAACCTTTA[A/G]TGTGTTTTCATTACT | 51444 |
| rs777265005 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119103 | GAAAAATTTTCCCCA[C/T]GTGATAAACCATTTG | 51444 |
| rs777361070 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32114359 | GATTTGGATTGATTT[A/G]TATCTTATCTCAGAT | 51444 |
| rs777431575 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090702 | ATAGATATGTAATAA[C/T]GTAAACAGGTTGAGA | 51444 |
| rs777476159 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32128512 | CACTGCACTCCAGCC[C/T]GAGTGACAGAGCCAA | 51444 |
| rs777499756 | snp | C/T | 3.32812e-05 | 0.00407915 | intron-variant | RNF138 | GRCh38.p7 | 18:32123583 | ATACAAGGTAAGCTT[C/T]TGAAAAATCCTGCCA | 51444 |
| rs777729000 | in-del | -/TTTC | 1.67458e-05 | 0.00289355 | intron-variant | RNF138 | GRCh38.p7 | 18:32123498 | TTGAGGTATTAACTT[-/TTTC]CCCTGTGCTTCTTAA | 51444 |
| rs777931706 | snp | C/T | 1.70612e-05 | 0.00292067 | intron-variant | RNF138 | GRCh38.p7 | 18:32111945 | TGTGACATCTCTCTT[C/T]TTTGGAAGCCAAGTT | 51444 |
| rs777972777 | in-del | -/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121142 | TGTCTCAAAAAAAAA[-/C]CAAAACAAAAAAAAA | 51444 |
| rs777981886 | snp | A/G | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32129147 | ATGAAGAAACCCAAT[A/G]CCAAACTGCTGTTGA | 51444 |
| rs778026567 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125455 | AGTGTTTCATAGGTA[A/T]GTTATTTCAGCTGTG | 51444 |
| rs778107302 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095142 | CAGTTGGAAGGAGTT[C/T]AGTGGGGGAATTGGA | 51444 |
| rs778226658 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117768 | GTTTTAGCAAAATTA[C/T]TGCATTGGTGTGGGG | 51444 |
| rs778228953 | in-del | -/TCTCGAAC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32116801 | TGTTGCCCATGCTGG[-/TCTCGAAC]TCCTGACCTCCGGTG | 51444 |
| rs778482563 | in-del | -/TTTTA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32106542 | AAAAATTATTTTTTA[-/TTTTA]TTTTATTTTATTTAT | 51444 |
| rs778554369 | snp | C/G | 2.67627e-05 | 0.00365795 | intron-variant | RNF138 | GRCh38.p7 | 18:32113723 | TATTTTAAATTAAAA[C/G]TCACATTTTAATAAT | 51444 |
| rs778568450 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093667 | GAGCCGAAATTGAGA[C/T]GCTACCCAGGGTGGG | 51444 |
| rs778679208 | snp | A/G | 1.72252e-05 | 0.00293467 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113857 | AAGATTCAGTAGGGA[A/G]CAGGTAAGCAATACT | 51444 |
| rs778688806 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32090977 | TATCCTTTTTTTGTT[C/G]TTCTTTTTTTTTGAG | 51444 |
| rs778691274 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100755 | TGTTGGGATTACAGG[C/T]GTGAGCCCCCGCGCC | 51444 |
| rs778878633 | in-del | -/ATG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110344 | TCTAGTGCTGCTTTA[-/ATG]ATATTAACTACTATT | 51444 |
| rs778910293 | in-del | -/TAG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096353 | GAACTAAGGAAATGA[-/TAG]TAGGAATGGAGCAGA | 51444 |
| rs779005983 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111428 | CTACTAAATGGCAGA[A/G]CCAGGATCCGGTTTT | 51444 |
| rs779067622 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | RNF138, RNF125 | GRCh38.p7 | 18:32090178 | TTCAACCTGGAAGGC[A/G]CAGGTTGAAGTGAGC | 51444 |
| rs779128549 | snp | C/T | 0.000213303 | 0.010325 | intron-variant | RNF138 | GRCh38.p7 | 18:32092899 | CGTGTGAGTAGACGC[C/T]CCCTCCCCCTCGCGG | 51444 |
| rs779136044 | snp | A/G | 1.64999e-05 | 0.00287222 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126726 | TCTCTTCCTTGGGGA[A/G]ATCCTAGCCAGATTA | 51444 |
| rs779255134 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32125689 | TGTAATTTAGCACTT[C/T]GGGAGGCCGAGAGGG | 51444 |
| rs779273917 | snp | A/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32119434 | TTATTTTATTTATTT[A/T]ATTTTTTTGAGACAG | 51444 |
| rs779291417 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32105574 | TATGTAGAATCTCTG[A/C]TGTGTGCTATACATG | 51444 |
| rs779346857 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112544 | TAAAAAATCAGCCAG[G/T]TGTGGTGGCGCATGC | 51444 |
| rs779378162 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant | RNF138 | GRCh38.p7 | 18:32129108 | GTTGACATGAATGTT[A/G]TTGTTTTTAGAATCT | 51444 |
| rs779521743 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097819 | TGAGCCACTATCCTC[A/G]GCCTAATTAATTAAT | 51444 |
| rs779640549 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32130520 | ATTTGCTGACATTCC[A/G]TACTAATATACATTG | 51444 |
| rs779691661 | in-del | -/TA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094782 | AATAGCTGCTAACTA[-/TA]TATATATATATATAA | 51444 |
| rs779708190 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | RNF138 | GRCh38.p7 | 18:32129096 | TATGTTTTTCCTGTT[A/G]ACATGAATGTTATTG | 51444 |
| rs779815082 | in-del | -/CACG | | | intron-variant | RNF138 | GRCh38.p7 | 18:32115766 | ACACACACGCACACA[-/CACG]CACGCACGCACACAC | 51444 |
| rs779815367 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094999 | TGATTGTTTTTAATT[C/T]AGGACCTTTCTCAAA | 51444 |
| rs779818111 | in-del | -/AT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100203 | GTTAGTGATTGAGAT[-/AT]ATATATATATATATA | 51444 |
| rs779934631 | in-del | -/TATAT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32111505 | AATATTTATTCATCA[-/TATAT]TATATTATGTTAAGA | 51444 |
| rs779939469 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109582 | CCCAGATTTGGTTAC[-/T]TTTACTATTTTTAAA | 51444 |
| rs779945092 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097404 | AAATTTGTGTAATTT[C/T]CTATTTGACCAGCTT | 51444 |
| rs779946594 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127357 | AAATGTGTGATATAC[-/TT]TTTTAATTAGGTGAA | 51444 |
| rs780009349 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100842 | ATGCCTGAGCTCAAG[C/T]GATCTGCTCGCCTTG | 51444 |
| rs780062639 | snp | C/G | 1.68457e-05 | 0.00290216 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32113844 | TTTCAGATCTCTCAA[C/G]ATTCAGTAGGGAACA | 51444 |
| rs780166210 | snp | A/G | 3.69447e-05 | 0.00429779 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092870 | ACGCCCGTGCGGACC[A/G]CGGCCTGTCAGCACG | 51444 |
| rs780223025 | snp | C/T | 8.67115e-05 | 0.00658394 | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092764 | CCATCGCCTTGTTTC[C/T]CCATCCCCCGCCATG | 51444 |
| rs780298695 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113937 | ACTATATGATAAGGT[A/G]TTTGGGGGGATGTGT | 51444 |
| rs780340512 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102293 | TGCAAGCTCCACCTC[C/T]CAGGTTCACACCATT | 51444 |
| rs780419695 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32109019 | TGGAATTTATGCGCT[C/T]TAATGGATATTGCCA | 51444 |
| rs780561962 | snp | C/T | 0.0373763 | 0.131496 | intron-variant | RNF138 | GRCh38.p7 | 18:32123591 | TAAGCTTTTGAAAAA[C/T]CCTGCCACTTTAGCA | 51444 |
| rs780564456 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32126307 | ATTTTTATTTTACTT[A/C]CAAATGAAATAAAAC | 51444 |
| rs780716957 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107915 | TCGCCCAGATTGGGG[C/T]GCGATCTCGGCTCAC | 51444 |
| rs780720605 | snp | A/G | 1.65206e-05 | 0.00287403 | missense, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32126708 | ACATGTCCTATTTGT[A/G]TGTCTCTTCCTTGGG | 51444 |
| rs780778782 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32102790 | GGTGCGCAACACCAC[A/G]CCCAGCTAATTTTTA | 51444 |
| rs780781811 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117604 | CACGTTATGAATATA[C/T]GGGAATTGGTAAAAC | 51444 |
| rs780785784 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32096084 | ACAGCGTAGTGGAGA[C/T]GGAGCTTAGCGTTAT | 51444 |
| rs780868035 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32118887 | CATGCATTGCAGATA[C/T]TTTTGTTTAGTCTTT | 51444 |
| rs780964222 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32104684 | ATAGCAACAAAATTA[C/T]AATGTTATTTGGACT | 51444 |
| rs780966675 | snp | A/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32092744 | CTCGGCCGCTGCCGC[A/T]GTCGCCATCGCCTTG | 51444 |
| rs781063443 | in-del | -/CTCCCGCT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32093113 | GCCCAAGCTCCCGCT[-/CTCCCGCT]CTCCCGCTCTCCCGC | 51444 |
| rs781071348 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127451 | TAAGATTAGTCCTGA[C/T]AAAGAATGGCTATTT | 51444 |
| rs781218881 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32095151 | GGAGTTTAGTGGGGG[A/G]ATTGGAGAGAAATTT | 51444 |
| rs781300995 | snp | A/G | 3.36508e-05 | 0.00410174 | missense, intron-variant, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32111786 | TCCTGACTGCAATGA[A/G]GGAAAGCGGAGCACA | 51444 |
| rs781323078 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32100594 | GATTTTCCTGCCTCA[A/G]CCTCCCAAGTAGCTG | 51444 |
| rs781414349 | snp | C/T | 0.000300797 | 0.01226 | utr-variant-5-prime, intron-variant | RNF138 | GRCh38.p7 | 18:32092654 | CCCCTTCCTGGCGCG[C/T]GCTGTATCCTGATGC | 51444 |
| rs781488612 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101214 | CCTCTTATAGGTTTC[-/T]TTTTTTTTTTTTTTT | 51444 |
| rs781664900 | snp | A/C | | | intron-variant | RNF138 | GRCh38.p7 | 18:32110683 | GTAATTTAACTGGTT[A/C]TCTTGAAAGCAAAAT | 51444 |
| rs781718235 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | RNF138 | GRCh38.p7 | 18:32131103 | TATGTCAAGTTAAAC[C/T]ATTCTGGGATTTGGG | 51444 |
| rs781752267 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32094018 | GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC | 51444 |
| rs781758298 | in-del | -/CCTGA | | | intron-variant | RNF138 | GRCh38.p7 | 18:32117127 | GGATGGTCTCGAACT[-/CCTGA]CCTCAGGTGATCCAC | 51444 |
| rs796228661 | in-del | -/AAT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32127094 | CAAGATTTAAGGGAA[-/AAT]TGTACCTACAAGAGA | 51444 |
| rs796265193 | in-del | -/TT | | | intron-variant | RNF138 | GRCh38.p7 | 18:32098927 | TGATTTTTTTTTTTT[-/TT]GAAGTTTTTTTGGGG | 51444 |
| rs796386870 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32099591 | TGTATTTTTAGTAGA[A/G]ATGGTGTTGCACCAT | 51444 |
| rs796599481 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | RNF138, RNF125 | GRCh38.p7 | 18:32091186 | TTGGCCAGGCTGGTC[G/T]TGAACTCCTGACCTC | 51444 |
| rs796648781 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32097928 | TGTGTGTGTGTGTGT[A/G]TATGTGTATGTATAT | 51444 |
| rs796700101 | snp | A/G | | | intron-variant | RNF138 | GRCh38.p7 | 18:32124322 | TGATGGAAGTCTTTT[A/G]GAAGTTTTAAGTTCC | 51444 |
| rs796891803 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32112131 | GAAAAAAAAATCACT[G/T]AATTTCATAATACTT | 51444 |
| rs796952085 | snp | G/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32101014 | TGGGTGAGTATCGAT[G/T]ACCCTTTCTTTAGGA | 51444 |
| rs796955794 | in-del | -/AC | | | intron-variant | RNF138 | GRCh38.p7 | 18:32121142 | CTGTCTCAAAAAAAA[-/AC]AAAACAAAAAAAAAG | 51444 |
| rs796960447 | snp | C/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32107219 | TCTGCCTCCCGGGTT[C/T]AAGCAGTTCTCCTGC | 51444 |
| rs797006221 | in-del | -/T | | | intron-variant | RNF138 | GRCh38.p7 | 18:32113376 | AACTTAATTTTTTTT[-/T]AAGTGCTTTCTAACT | 51444 |