| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs114333209 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180010915 | TTAAACTGGAGAGGT[A/G]GGGAGATTTCAGTGT | 55819 |
| rs114333586 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | RNF130 | GRCh38.p7 | 5:179947109 | CCATACCTGGGTTTC[C/T]AGAATCTTCTCATCA | 55819 |
| rs114333716 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179975761 | TAACAGTACCATAGA[C/G]GGTGCAGCGAAATTC | 55819 |
| rs114340659 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179961061 | TCTTTCCTATCATCT[A/G]CCACAATAAAAACTG | 55819 |
| rs114352058 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | RNF130 | GRCh38.p7 | 5:180052300 | AGCAGTCCAAACTTA[C/T]TAGCTTCCTCTCACA | 55819 |
| rs114362050 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF130 | GRCh38.p7 | 5:179965303 | ACACAGTGGGTGCCA[A/G]CGGGAGGCACTGTGG | 55819 |
| rs114371021 | snp | A/G | 0.0158469 | 0.0875917 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954568 | TTTCCAGGGCTGGCA[A/G]GGGTGAGAAGTTACT | 55819 |
| rs114403010 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180046731 | GATTCTGCCAAAATG[G/T]CTTCTCCAGAACGCT | 55819 |
| rs114445829 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179973026 | AGAAAACCTCCCTTC[C/T]TCAGCTAAATGAAAA | 55819 |
| rs114502502 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180047808 | CCTGCCCCAGCCAAG[C/T]GCTCTCCTCTCTCCA | 55819 |
| rs114503254 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180067123 | GTCTTGAGGCCCAAA[G/T]GCAGCGCAAGATTAG | 55819 |
| rs114535479 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:180003282 | GAGCCGTGTGAGAGC[A/G]CCTGCCATCACACTG | 55819 |
| rs114558593 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179963995 | TTAGTCAAAGGCTGA[A/G]GAGCACGGAGCAGCA | 55819 |
| rs114584908 | snp | A/G | 0.0217236 | 0.101931 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180074027 | TTCAAACTGTAAGGT[A/G]CCCATGACCCCTGGC | 55819 |
| rs114592109 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180005104 | GTCTCTCGCACCAGA[A/G]AAGAATTGTATATCA | 55819 |
| rs114603477 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179942410 | ATCTCCAAATTTTGG[A/G]AAAAAAGAATATATG | 55819 |
| rs114664291 | snp | A/G | 0.000745851 | 0.0192969 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920302 | TGACCCCAACAGCCA[A/G]GCCATGTTTAAAATT | 55819 |
| rs114672801 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:180038469 | TTGGATTATAGGATT[A/G]CAGGTGTGAGCCACT | 55819 |
| rs114700124 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | RNF130 | GRCh38.p7 | 5:180061570 | AGCGTCTGATGGCTG[C/T]TAGCCATCCTTTGCA | 55819 |
| rs114717950 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:179961156 | CAAATTGAAGAAGAC[A/G]TTGCCCCAGATTCTA | 55819 |
| rs114791843 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:179946877 | GATCTTTTCATCAGC[C/T]GGGTTTGCCTTTATC | 55819 |
| rs114797204 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:180020255 | CAGGTGGATTCTCAA[A/G]TTGCCCAGGATGGTG | 55819 |
| rs114808342 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | RNF130 | GRCh38.p7 | 5:180025523 | AAAGAAAATTAAGAG[C/T]TTATGGAAGTTTTAA | 55819 |
| rs114819798 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179923361 | ATTGTAAATGTGTGG[G/T]TCTATTTCTGGGCAC | 55819 |
| rs114825761 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180069533 | ACCCAGTCTTCACAC[A/G]CTGCCCAAATGTGTT | 55819 |
| rs114826348 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179929839 | AATCACAGTAAGTCT[A/G]TAAGTCACTTTGGGG | 55819 |
| rs114874204 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179952219 | ACAAAAAAACAAGAT[C/T]TGAGTAAAAATTAAT | 55819 |
| rs114874525 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:180066840 | TCTGTCTCTAAAAAA[C/T]AAAATACAATAAAAA | 55819 |
| rs114887232 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180036038 | TATAGACAGTTTCTA[C/T]AGACTTTTGTTTTCC | 55819 |
| rs114894500 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RNF130 | GRCh38.p7 | 5:180060531 | TGATTAATGGAATAA[C/T]GCCCAGCAGCCTAGA | 55819 |
| rs114903157 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | RNF130 | GRCh38.p7 | 5:179979244 | TGCTGCTTCTATTTT[C/T]TTAAGTGATTTCCCC | 55819 |
| rs114903697 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179937368 | AGCAAAAGACAACCT[A/G]ATTAAAAAATGGGCA | 55819 |
| rs114934688 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:180009463 | ATTTCACTGAAGAGG[A/G]TATACGGATGGCAAA | 55819 |
| rs115009258 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:179999460 | GCCATGGTGGCTTAC[A/G]CCTGTAATCCCAGCA | 55819 |
| rs115014404 | snp | A/T | 0.021333 | 0.101051 | intron-variant | RNF130 | GRCh38.p7 | 5:180026271 | AAAATTCTTACAGAC[A/T]TACAGATAAAACTAC | 55819 |
| rs115025115 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179925262 | CGGAGAGGGGCTGAA[A/G]GTTAAGTTGATCGCC | 55819 |
| rs115046056 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:179943958 | GTAACTAACCACTTC[C/T]CTTTATTTCTGAGAA | 55819 |
| rs115050190 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180061289 | AAAACCACAACAACT[A/G]ACGTGACTTCAGGCA | 55819 |
| rs115065307 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:179994482 | AAGCAATTGTGAATG[C/G]GAGTTCTGGAGTGGA | 55819 |
| rs115066968 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF130 | GRCh38.p7 | 5:179974244 | AGCGGCCGGCCCCCC[A/G]CTTTAGCTCCTGAAG | 55819 |
| rs115126480 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180050523 | TTCTCTCAGGATACT[A/G]TCTGACCAAGTATGT | 55819 |
| rs115128588 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180002086 | CATTTCCCTGTGATG[C/T]TGGGAGCTGCTTCAG | 55819 |
| rs115187615 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179946060 | TCCCATCAGCGTTTC[A/G]CTGTCCTCCAAGGGA | 55819 |
| rs115197209 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180024750 | AGAACTGTTAGTATG[C/T]AGGCAAACATAAAAG | 55819 |
| rs115200074 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:179961212 | TGAGCATCCTTGCTC[A/G]TATCCACATGCGTGC | 55819 |
| rs115207335 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179928397 | AGCAGGTGTATACAC[A/G]GCATTTCACTATGTT | 55819 |
| rs115237878 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946274 | ATGTGTCTAGGCTGT[C/T]CCTGCCATAGCCGCG | 55819 |
| rs115238125 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179954315 | TTCACAGCAACATTC[A/G]TAACAGCCGAACAGC | 55819 |
| rs115256970 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180046699 | ACCACTCTTGCTCAC[C/T]ACCTTCTGAGCCTCA | 55819 |
| rs115365361 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180028819 | TAAACAATTAAGTTA[C/T]ATGGAAAAACACCAG | 55819 |
| rs115398612 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180057218 | GGCAAGGGGCTAAAG[A/G]TTGAGCCAATCCAAT | 55819 |
| rs115400045 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179995573 | ACTGGAGTCCTCTTA[C/T]CAGCCACCAGGTCTG | 55819 |
| rs115400403 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180005148 | AAACCGTACTGATGG[C/T]CCGGCGTGGTGGCTC | 55819 |
| rs115420861 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180003602 | CATTTCCCATCACTT[C/T]GCGACAGGTAAACCT | 55819 |
| rs115435937 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179996523 | TGTTAAGAGTTCATA[C/T]CATGAAGCCACTTAT | 55819 |
| rs115439856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059157 | CACAAGTACATCACA[C/G]TTTTTGCACCTTTTA | 55819 |
| rs115460286 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:179999493 | TTGGGAAACCAAGAC[A/G]GGCGGATCACCTGAG | 55819 |
| rs115464340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976441 | TGTTGAAGCAGGCAA[A/G]TGTGGATGACGCCTC | 55819 |
| rs115481044 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180053012 | AAAAAAGGATTTTAT[A/G]TCAAGATAATGTACG | 55819 |
| rs115481256 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179965961 | GCCTCAGGGCGTGAC[A/G]TGCTAGGCAAGCAGC | 55819 |
| rs115502059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946847 | ACGTCAGCCACCGCG[C/T]CCAGCACCATAGGGG | 55819 |
| rs115517486 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180008230 | TCCGCTAGCCAAAGT[A/G]CCAAGAGAAGGATGG | 55819 |
| rs115544989 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180042500 | GAAAGACACAGACGA[C/T]GCACTATAAAACTTT | 55819 |
| rs115554473 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:179922064 | AAAAGATGGCCCTAC[C/T]GGCAGCCTATGGTAG | 55819 |
| rs115593097 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179991635 | TCTAGATCAGTGGCC[C/T]CCAACCTTTTTGGCA | 55819 |
| rs115594098 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180059670 | CAGAGCACTGATACG[A/C]AACAATGAAGGTGAG | 55819 |
| rs115608109 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180070603 | GTGACAATGAGGGTG[C/G]GGATAATGGCAGATA | 55819 |
| rs115638019 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:180025256 | TCAGTTAAGAACATC[C/T]TCCGTCCTGGAACCT | 55819 |
| rs115709621 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016379 | TTCACAATAAAGGGC[C/T]GGTCAGAGGAGGCAG | 55819 |
| rs115744536 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969253 | AGTGTTGACCTGGCA[C/T]CTGCCACAGCTGGAC | 55819 |
| rs115756131 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180049336 | ACAAGGCTCTGGGGA[C/T]AGAATTCAGGGCTGA | 55819 |
| rs115758113 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180037184 | TGCAGGTGTTTTCAA[C/T]AATCTGCTGTTACAA | 55819 |
| rs115801894 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF130 | GRCh38.p7 | 5:180018751 | TGCCCAGGGATCTGC[C/T]GACCAACACAGTCCT | 55819 |
| rs115865631 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | RNF130 | GRCh38.p7 | 5:180053968 | CCGAGTAGCTGGGAC[C/T]ACTACACCCAGCTAA | 55819 |
| rs115868212 | snp | A/T | 0.0287284 | 0.116357 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072997 | CATCGCTATAAAGTA[A/T]CAGCTAAAAGGAAGA | 55819 |
| rs115897957 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179965747 | TTTTCTCTATTGCAT[A/T]GCTGAATGAAGCCTC | 55819 |
| rs115929694 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:180052776 | TAAAATCAGTCCCTA[C/T]GGAGGATTACAGAAA | 55819 |
| rs115935502 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180002592 | CTGGTGGGAACCCTG[C/G]TGGTGAGGTCTGTAG | 55819 |
| rs115939843 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960182 | GACCTCTTTTGGGAA[C/T]TGAAATTCAGTAACC | 55819 |
| rs115946253 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:180067957 | TACATTTTTAAACAT[A/G]AAAACCTAAGATTCA | 55819 |
| rs115947525 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180011997 | GCAGTCAGTGTTTGG[A/G]TATTTTATATGTACT | 55819 |
| rs115974812 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180011023 | ACAAGGAGAAATGAG[C/T]GAAGGGGATAAGAGA | 55819 |
| rs116012384 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179986754 | TGGATTTTTGTATAT[G/T]TTATGATAGTAAATG | 55819 |
| rs116055234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179935148 | TTTAATTCCAAACAT[C/T]TGGGGATCATTCTAA | 55819 |
| rs116111019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179947055 | CAAGTGCACACTGAC[A/G]CAACCCTACTGTACT | 55819 |
| rs116140603 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:180049450 | ATAACAAACCATCTG[C/T]AACTCTGTAACCAGC | 55819 |
| rs116160700 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RNF130 | GRCh38.p7 | 5:179923607 | GCCAACAGTGCAAAG[A/C]GTGTTCAGTGAGGCA | 55819 |
| rs116175869 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179960659 | GCTTGAACAGTAATA[C/T]ACAAGAACAGTGACT | 55819 |
| rs116180867 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180020733 | AAGAGAAAGAAAAGG[C/G]GGCAGGAGCAAGCAC | 55819 |
| rs116211141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981376 | CCTGACGGAGCAAGG[C/T]GGGGACCAAAACAAC | 55819 |
| rs116224699 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:180042175 | CTTACACGACTTAAA[C/T]TGTAAAATGTAAAGA | 55819 |
| rs116239574 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | RNF130 | GRCh38.p7 | 5:180002673 | CCACAGTGAGCTCTT[C/T]CTGGTTCCCAGCTGA | 55819 |
| rs116278807 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:180003267 | TTCTGGCTCGGTGAT[A/G]AGCCGTGTGAGAGCG | 55819 |
| rs116282402 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179963116 | ATGTGTGTGATGAAC[A/G]CAAAGTGGGCTCTTC | 55819 |
| rs116312214 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180037229 | CCTACGTGTCGTCCA[C/T]GCACATGTGCGAGAG | 55819 |
| rs116361925 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179991210 | TTATAGATGACTAGG[C/T]GCTTTTCTCTTGTTG | 55819 |
| rs116365960 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179973450 | CAACAGTCTGGTGCT[C/T]GGCAAACCACCTTTC | 55819 |
| rs116367771 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034623 | AATTTGTCAGTATAC[A/G]GAAAAAAGTAAACAT | 55819 |
| rs116378233 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:180059907 | AGGTTACAGAGCAAG[G/T]GGGAACTAGGTTGCA | 55819 |
| rs116401803 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179952805 | TATTTCATGATAAAA[A/C]CGTTCAATAAGCTAG | 55819 |
| rs116435346 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179983833 | AATAGTTAGTTTTCA[C/G]TACATAGGGCATATT | 55819 |
| rs116437228 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | RNF130 | GRCh38.p7 | 5:180031579 | CTAACCTTCTCACTG[C/T]TCAAGGGCCAACTGT | 55819 |
| rs116439920 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RNF130 | GRCh38.p7 | 5:179939723 | CCACTTCCAAAAGAC[A/G]GAAATCCACTGAAAG | 55819 |
| rs116452264 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179968739 | CAGATGCTCTATGTT[A/G]GACCAGTCTGAAATG | 55819 |
| rs116463976 | snp | C/G | 0.213937 | 0.247385 | intron-variant | RNF130 | GRCh38.p7 | 5:180057519 | TACCACTGCGCTCCA[C/G]CCTGGGTGACAGAGC | 55819 |
| rs116473066 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | RNF130 | GRCh38.p7 | 5:179974525 | ACGTCACGTGGCAAG[A/C]AGCAGGCAATCCATG | 55819 |
| rs116486220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955967 | ACAATTTACAATTTT[G/T]CCTGGTTTAAACACA | 55819 |
| rs116505639 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180002159 | CCACTTCCTGGGAGG[C/T]GTGGCGCTGCTTCAA | 55819 |
| rs116524457 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | RNF130 | GRCh38.p7 | 5:179942862 | CTCTCTCCTGTGGAT[A/T]TAAGATAGGGCTTTT | 55819 |
| rs116548699 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055453 | CTTTGTGTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 55819 |
| rs116554352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180069046 | AATACCCAAGTATTC[C/T]AATTTTAAATCATTT | 55819 |
| rs116565981 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:180067469 | AACGTTTAGAGGTTC[A/G]CTGTAAGAGAGAAAT | 55819 |
| rs116589847 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180055026 | AGTTTTTAAAAAATT[A/G]CTCTGCTGGTTATTG | 55819 |
| rs116591336 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180004558 | GGGGTTTGTTAGGGG[A/C]CAGATTATCTTATCT | 55819 |
| rs116592272 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179960894 | TATTGGTAGATAAAG[A/G]CAAAAACAGAAATAA | 55819 |
| rs116592822 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179998128 | AGAGGCGTGAGCCAC[C/T]GTGCTTGGCCTGTTT | 55819 |
| rs116608731 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179944675 | GCTGAGGTGGGAGGA[C/T]CTCTTGAGTCCCAGA | 55819 |
| rs116647742 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:180020456 | CACAGCAAAGACCAA[C/T]CTGTAATTTTGCAAA | 55819 |
| rs116670376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047481 | CCGGCGTGGTGGTTC[A/G]TAGCTGTCATCCCAG | 55819 |
| rs116709310 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974845 | GGCACGCAGCGGCGC[A/G]GGGAGGAGCGGCATG | 55819 |
| rs116714127 | snp | C/T | 0.0130921 | 0.0798413 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954716 | TTATAGCATGTGAAT[C/T]ACATTTTGATTGCAA | 55819 |
| rs116715504 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179946072 | TTCGCTGTCCTCCAA[A/G]GGACTTTTCAAATGC | 55819 |
| rs116733237 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:179925356 | GGGACTGGGATACTT[C/T]GGGGATAGCTAAACA | 55819 |
| rs116740406 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180024983 | CTTAGCAGGTCCACA[C/G]CTGGGAGGTGAAACA | 55819 |
| rs116744697 | snp | C/T | 0.029116 | 0.117091 | intron-variant | RNF130 | GRCh38.p7 | 5:180014246 | GAATACCTCTTCCTA[C/T]GGACAGCAGGAAACT | 55819 |
| rs116778091 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF130 | GRCh38.p7 | 5:179923841 | TTAACAACACTAACA[C/T]CATATTGTCTTGATT | 55819 |
| rs116782725 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180009670 | TGAGTCTAACAGTTT[C/T]CTACAGAACTAAATA | 55819 |
| rs116840136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179970088 | TGAACCCAGGAGTTC[A/G]AGGTTACAGTAAGCT | 55819 |
| rs117139494 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RNF130 | GRCh38.p7 | 5:180071075 | CAGCCTTAAGTCCGT[C/G]ATTTGAGGAACCTGC | 55819 |
| rs117200699 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955136 | TGCAGGGGCACAGTG[A/G]GGAGCAAATGTTACA | 55819 |
| rs117236482 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179969859 | AGCCAGGGGTGGTGA[C/T]GGGCACCTGCAATCC | 55819 |
| rs117238753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044519 | TACAATGTGGCAAAC[A/G]CCTTGCTCTTGACTC | 55819 |
| rs117265593 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180068377 | CCTTCAAAACTCCGT[C/T]TCTAAACACGAATTC | 55819 |
| rs117439042 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | RNF130 | GRCh38.p7 | 5:179921341 | CTAGAATTTTATATA[A/G]GTAGAATTGCATAGT | 55819 |
| rs117527564 | snp | G/T | 0.0327778 | 0.123752 | intron-variant | RNF130 | GRCh38.p7 | 5:180050650 | CTTATTCTACATCCT[G/T]CAGAAGTTCTTTCAA | 55819 |
| rs117536854 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179973461 | TGCTCGGCAAACCAC[C/T]TTTCTGCTGTGCAGA | 55819 |
| rs117553984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180063545 | GAAGTAAAGATACCA[A/G]TAGGAAGCCAAGCGC | 55819 |
| rs117633083 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179957696 | AGCCCTACTTTATTC[C/T]TTTGTGTACATATAT | 55819 |
| rs117688939 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179978538 | TTACAAAAATTAAGT[C/T]GGAATTCTAATTTTT | 55819 |
| rs117699147 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180039936 | AAAACTCATCGCACA[C/G]CGCCTGGCATTTATA | 55819 |
| rs117722055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032323 | TACATTTTGTCTAAT[A/G]TCCAAGTGAAGTCAT | 55819 |
| rs117810645 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | RNF130 | GRCh38.p7 | 5:180053308 | CAGCTGCCCGAACCC[A/G]ATGCAGGCCCCGAAC | 55819 |
| rs117936581 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179987286 | CATCCTCCTGCCTCA[C/G]CCTCCTGAATACCTG | 55819 |
| rs118077410 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF130 | GRCh38.p7 | 5:179930464 | ATATATTGAATTTTC[C/T]ACATGTAATCGTTTT | 55819 |
| rs118109046 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:180067853 | CCAAATCCTGTTTTC[A/G]CATCAATCTCCTCCA | 55819 |
| rs137855742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063360 | TTAGATGTGGAATGT[A/G]AGCCAAAGAAGCAAG | 55819 |
| rs137863155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010994 | TACTGACCACAGTTA[C/T]ACATGTTGTTACCAC | 55819 |
| rs137888534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936119 | AAAATGTCTTATTTC[A/C]TCTTTCTTTTCTCTT | 55819 |
| rs137890529 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014942 | AGTGAGCTGAGATCA[C/T]GCCACTGCACGCCAG | 55819 |
| rs137922168 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179939661 | TGAAGTGAGGCCCTG[C/T]GACCTAGTGATCCAA | 55819 |
| rs137966598 | in-del | -/CTAAGA | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180046758 | CGCTTTCCCAGCCTC[-/CTAAGA]CTGAGTTGGGTGCTT | 55819 |
| rs138030477 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179956040 | TTAAAAAATGCTCCT[C/T]TTACCTCTCAAACAA | 55819 |
| rs138034666 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180037768 | CTATACCACATAATG[C/T]CAAATTTCTCTCCAA | 55819 |
| rs138048850 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:180056205 | TATAGATTTATTCCC[A/G]CTGTTACTCTTAGCC | 55819 |
| rs138068648 | snp | C/G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072518 | GACCTCTAGGGTAGC[C/G/T]GTCCCTAACCATTTT | 55819 |
| rs138092483 | in-del | -/CA | 0.0150606 | 0.0854603 | intron-variant | RNF130 | GRCh38.p7 | 5:180047865 | TTCCTCCTGCACTAC[-/CA]CAGTCATTCTTTGGG | 55819 |
| rs138102823 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179975120 | TGAGGGAACAGAACC[A/G]CTTAGCAACATGAGG | 55819 |
| rs138122722 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179940519 | TGGGATTACAGGCAT[A/G]AGCCACTGTGCCCGG | 55819 |
| rs138126559 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179988186 | GGTTGTATGTGGCTA[A/G]GAATGTATCCATTTT | 55819 |
| rs138140206 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:179962391 | TTTCTATAGCCAGAC[A/T]ATGGGCAGTCAATTA | 55819 |
| rs138160789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060134 | GGAAATGATTCCCCC[C/T]GAGAGCTCCAAAGCC | 55819 |
| rs138171639 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180044442 | ACCAAACAATTCTGG[G/T]CTCCTCACCTCAATG | 55819 |
| rs138177139 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | RNF130 | GRCh38.p7 | 5:179944501 | TGGAGTCTTGCTCTG[C/T]CGCCCAGGCTGGAGT | 55819 |
| rs138228883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995349 | CTGCTCCAGTCCCAT[A/G]ATGGGGGTGCAGGGG | 55819 |
| rs138344638 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180003046 | GATGCTATTTGAGGC[C/T]TGGAGAATTAAAATC | 55819 |
| rs138347588 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179998539 | TTGGACTCATGAGAT[A/C]CTTTCTGCCTCACCT | 55819 |
| rs138384972 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179943640 | ACAGAAAAGGTGAGG[C/T]TCAGAGAGATAAAAT | 55819 |
| rs138394675 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180059606 | AGAAGGTGCATCACT[C/G]ACCTTTAAGGAGTCA | 55819 |
| rs138427597 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | RNF130 | GRCh38.p7 | 5:179930246 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCACGT | 55819 |
| rs138442330 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF130 | GRCh38.p7 | 5:180048527 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 55819 |
| rs138462336 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179970272 | GTCCTGTTGGGCTTA[-/C]ATGGTTACATGGCAA | 55819 |
| rs138475011 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179967438 | CTAAAAGCCCCATTT[A/G]TCTGGTAGTCAGTTT | 55819 |
| rs138484274 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919875 | CCAGAGCCAGGTCAG[G/T]GAGCAGCACCTGTAC | 55819 |
| rs138485086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179971148 | TCACAGTCTTGTGAC[C/T]GGAAATAAGTCAGTC | 55819 |
| rs138488686 | in-del | -/TATTT | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179986894 | TTTATTATTCTTATG[-/TATTT]TATTTTTATGTGACT | 55819 |
| rs138489014 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:180055603 | TCCGTTTGTTTTCAG[A/G]TAATACTGCCAACAG | 55819 |
| rs138524448 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RNF130 | GRCh38.p7 | 5:179923247 | TGAAGTTCATTTTTT[C/T]TTTTGCATATGGATA | 55819 |
| rs138526362 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180020884 | TTGCCAACTTTCAAC[A/G]CAACACAGGAACTCC | 55819 |
| rs138531604 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974692 | TGTGGGGCAGTACTT[C/G]GAGGGCGATGGCTTT | 55819 |
| rs138546829 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180010653 | GTGTGAGCCACCGTG[C/T]CTGGCCCATGATTCC | 55819 |
| rs138570499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978020 | GGCCGTGCAGCCCGC[A/G]CCTGCTGAACAGCAC | 55819 |
| rs138603929 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180064482 | GGTGGTCTATTCCAC[A/C/T]GTTCCAAACAGGTCT | 55819 |
| rs138665033 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179936452 | CAGGCTTGTCTTGAA[C/T]GCCTGAGCTCAAGCA | 55819 |
| rs138680885 | in-del | -/TCTT | 0.0283406 | 0.115616 | intron-variant | RNF130 | GRCh38.p7 | 5:180050708 | TTACATCTGAAAACA[-/TCTT]TCTTTTGTTCTCATT | 55819 |
| rs138777699 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180028137 | TTCACTTACAAGGGG[A/C]CTTTGGCCTAGAATA | 55819 |
| rs138778225 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015987 | ATTACCTGCTCTTGA[G/T]GCAAAAATCCACACG | 55819 |
| rs138810095 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179998894 | ATATATGTTTTATAT[A/G]TCTGAGTGCTCCAGT | 55819 |
| rs138818667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945506 | ACACACACCATGTTT[C/T]CAATCCTCACAGTGC | 55819 |
| rs138819308 | in-del | -/TTCAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034592 | TTTTTAGGAATTTGT[-/TTCAT]TCATCTAAGGTGTCT | 55819 |
| rs138819997 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179956757 | CCAGAAGGGCCTTTG[C/T]GTACTCCCTCACTCT | 55819 |
| rs138830887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949556 | TTGCATTACAAAAGT[C/T]TGTCCAAGAAGGGTT | 55819 |
| rs138841723 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:180033006 | TTGAGACAGGGTCTC[A/G]CTCTGTTGCCCGGCG | 55819 |
| rs138850357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961664 | GAACTTTTTAAGAAG[C/T]AGGCTTGTATTACTA | 55819 |
| rs138874429 | snp | A/G | 0.00288006 | 0.0378383 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966978 | GAGCCTTTCCATATC[A/G]AATGCTACGTTATCA | 55819 |
| rs138960112 | snp | C/T | 0.000543465 | 0.0164753 | missense | RNF130 | GRCh38.p7 | 5:179966926 | CGCCGGCGAGGTCGC[C/T]GAGGGCTGATCTTCG | 55819 |
| rs138965838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180048342 | CTGTTTCCAGGTTGC[C/T]CTGCCCTGCTTCTAG | 55819 |
| rs138989485 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:179964737 | GCTCCTGGGGACTTC[C/T]GGTCCAGAGAGTGCT | 55819 |
| rs139030404 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055290 | AAAAAACAAAAAAAA[A/C]CAGCAAACAAACAAA | 55819 |
| rs139033176 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179995809 | GAGGGCTGTCTCCCA[A/T]ATTTCTCTTTCCCAG | 55819 |
| rs139061421 | in-del | -/A | 0.040671 | 0.13668 | intron-variant | RNF130 | GRCh38.p7 | 5:179971028 | AGCTGAAACTATTTT[-/A]AGGGGTAAACTGTGC | 55819 |
| rs139220617 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180006541 | ATGGCAAGAAGCTTT[C/T]ACAAATTTTAAATAC | 55819 |
| rs139231705 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179924504 | TGTCTGAAAAAAAAA[A/T]AAATAAATACAGGCT | 55819 |
| rs139240151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004654 | AATTGGCAGAAAACA[A/G]GTTAAAACAATTCTT | 55819 |
| rs139253744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009712 | TAACAGCCCAAAAAC[C/T]TCACTCTTGGAATTT | 55819 |
| rs139254785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969187 | GCATAACCCTGGCTA[C/T]ACATGCTTCTCTTAA | 55819 |
| rs139262425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946070 | GTTTCGCTGTCCTCC[A/G]AGGGACTTTTCAAAT | 55819 |
| rs139264365 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180028773 | AAATCGATACCTGTT[A/G]ATTAACTATTTTTTT | 55819 |
| rs139268904 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180051963 | GTGTCACAGTGCAAT[A/G]TAAGTGTTAATTGTT | 55819 |
| rs139295459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061344 | AGCTCGACTCTCTCC[C/T]GTGCTGGCAAAGCTA | 55819 |
| rs139306341 | in-del | -/CTTT | 0.021333 | 0.101051 | intron-variant | RNF130 | GRCh38.p7 | 5:179987159 | TCCTTTCCTTCCTTC[-/CTTT]CTTTCTTCTATTTTT | 55819 |
| rs139319900 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179973330 | CTGAACACGGCACCT[C/T]TTTCTCCTCATCACC | 55819 |
| rs139326265 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | RNF130 | GRCh38.p7 | 5:179932406 | GGGACTACAGACATG[C/T]GCCACCACTCCCGGC | 55819 |
| rs139328368 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180012129 | ACTGTCCAACAGGGT[A/G]AGGGGTCATGGTGAA | 55819 |
| rs139335692 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996530 | AGTTCATATCATGAA[A/G]CCACTTATCAAATGC | 55819 |
| rs139365711 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179952112 | CTGAGGTAGGAGGAT[G/T]GTTGGAGCCAGGGAG | 55819 |
| rs139370339 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981082 | GTTAGATGGGAAAGG[A/C/T]GTAGGGTTAGGAGGG | 55819 |
| rs139384277 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057282 | GGGTGGGCACAGTGG[A/C]TCACGCCTGTAATCC | 55819 |
| rs139438359 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180001268 | AATGAGGAGACTTAG[C/T]CAAAGTGATCCCTCT | 55819 |
| rs139438644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926597 | AGGTGGCAGTGAGCC[A/G]AGATAGCGCCATTGC | 55819 |
| rs139464495 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179990806 | CTTCAGCTACTATCT[C/T]TGTATGGCCTGGTTT | 55819 |
| rs139479443 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180049913 | TTTTTTAGTGCCTAC[C/G]CTTAAAATGTTAACA | 55819 |
| rs139545452 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179926871 | TTTCCAGGTAGACAG[A/C]GTTGGAACTGAATTG | 55819 |
| rs139590105 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179920578 | GAGATACAAAAAGTG[C/T]GGGCATCCTTCAATT | 55819 |
| rs139596086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999941 | TATTTTTGTTCTCTC[C/T]TATTGTTTATCATTA | 55819 |
| rs139617599 | in-del | -/GT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937914 | GAATCTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 55819 |
| rs139629991 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066846 | TCTAAAAAATAAAAT[A/C]CAATAAAAATAAAAA | 55819 |
| rs139656994 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180031026 | AGGATGAAAACCATT[A/G]TGGTGATGTGACCAA | 55819 |
| rs139660381 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180050919 | AGTAATCCTCCCACC[A/T]CAGCATCCTGAGTAG | 55819 |
| rs139701291 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:179984254 | TCTCCATTTCCACAA[C/T]GGATGTCTTTTACGT | 55819 |
| rs139717424 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931058 | AAAAAAAAAAAAAAA[-/TC]AAGAATAGGTGTTGA | 55819 |
| rs139778078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986265 | TATGTGTTTTACAAT[A/G]ATATGCTAAGTCATT | 55819 |
| rs139810227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179971953 | CTTGAAGAATGAATT[C/T]ATCAATCTAGTCTTA | 55819 |
| rs139816934 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:180042095 | AGATAAAGAGATGAC[A/G]CCAGTGGGAAAATGT | 55819 |
| rs139820081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179973463 | CTCGGCAAACCACCT[C/T]TCTGCTGTGCAGAGG | 55819 |
| rs139824246 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180057657 | GGATTATTACACCCC[C/T]GCAATACCGCGACAG | 55819 |
| rs139826872 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022902 | AAGAAACATTAAGTA[A/G]AGAGTTCGGCATTCT | 55819 |
| rs139876429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958922 | CTGACCTCAGGTGAT[C/T]TGCCCACCTCAGCCT | 55819 |
| rs139895667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180007126 | TTTGTGGGGGCCAGG[C/T]GTGGAGGTTCATGCC | 55819 |
| rs139897204 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179976310 | CTCATTCTAGTAATA[C/T]ACCCATGAATGGTTT | 55819 |
| rs139932021 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180011585 | AGCCTGGCCAACACT[A/G]CAAGACCTGGCCTGT | 55819 |
| rs139966208 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023814 | AAGGGAGATGGAGCA[A/C/T]AAATCCCCACTTATT | 55819 |
| rs139988325 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179968863 | TGCTGAACGGTCTAC[A/G]ATGCACAGGACAGCC | 55819 |
| rs140004601 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934541 | TTTCTTTTCTTTCCT[-/T]TTTTTTTTTTTTTTT | 55819 |
| rs140023491 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179951353 | CTAACACACGTCTAC[A/G]GAACAGTCCATCCAA | 55819 |
| rs140107867 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179986642 | TACAGTACGTACTAC[C/T]GTTAATTTTATGCGG | 55819 |
| rs140112707 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073748 | CGGGGTCCTCGCCCT[A/G]GGCCTGGCACCTAAA | 55819 |
| rs140140449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179991313 | AATCTGATGACTATA[C/T]GTCATGGTGAAGTCC | 55819 |
| rs140178809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031853 | AAACTGGTTGTACCA[C/T]TTCACATTTCTACTC | 55819 |
| rs140198965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014687 | AGACTACACGCAACT[A/G]AAAAGAAATTCAACA | 55819 |
| rs140246311 | snp | C/G/T | 0.000133321 | 0.00816359 | synonymous-codon, missense | RNF130 | GRCh38.p7 | 5:179966846 | TGTTCTCGGAGTGAG[C/G/T]TCCCCATCCTGAGGA | 55819 |
| rs140277174 | snp | A/T | 0.000214591 | 0.0103561 | intron-variant | RNF130 | GRCh38.p7 | 5:179978152 | CCCTGAAAAGGAGGC[A/T]TACAAAGCACATTAA | 55819 |
| rs140313350 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179981463 | AAGTTTTAAACACAC[A/T]AAAGAACAGAGAATG | 55819 |
| rs140349187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921738 | GGAGGTGGAGGTTGC[A/G]GTGAGCCAAGATCGC | 55819 |
| rs140376768 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180041479 | GTAAGCGCCTCAATT[G/T]TTCACTCTGCACATA | 55819 |
| rs140379892 | snp | A/C | 0.00953873 | 0.0683987 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955152 | GGAGCAAATGTTACA[A/C]GTCCCTGCTGCTGGG | 55819 |
| rs140424843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179923011 | ACTTGCCTTGACATT[A/G]TTATAACAATGTCTT | 55819 |
| rs140429722 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180002917 | AGGTAACTCAGATCT[C/G]GGTTGTTATTATTAT | 55819 |
| rs140445335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180045316 | CAAGAAGGAAGCCGC[A/G]GACCCTCACGGTGTT | 55819 |
| rs140589192 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179961859 | CAGATGGTCATCTGA[C/T]TCACACAACTTCAAT | 55819 |
| rs140607723 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054394 | CCTCCAGGCCAGGGT[C/T]AGATGCAGATGCCCA | 55819 |
| rs140611478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180047354 | CTTTATCCACTTCCA[C/T]GGATATAACTTATTA | 55819 |
| rs140630839 | in-del | -/A | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:180010731 | GATTCCTGGTAGATT[-/A]GGGAAGGGGGAAGGA | 55819 |
| rs140631454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966250 | TTTCAGGCAGATTGT[C/T]CTTTGGCTTTTCTCC | 55819 |
| rs140645406 | in-del | -/TATT/TATTTATT/TATTTATTTATT/TATTTATTTATTTATT | 0.457388 | 0.139608 | intron-variant | RNF130 | GRCh38.p7 | 5:180051238 | TTTGTATAGATATTA[lengthTooLong]TATTTATTTATTTAT | 55819 |
| rs140667681 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180036246 | AATCTATTTTCACTG[C/T]GATGTGCAACCATGA | 55819 |
| rs140727094 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179937681 | AGAATTCTATGACCC[A/G]GCAATTCCACTGCTA | 55819 |
| rs140773929 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180070245 | CAAAAGTTGTTTCTA[C/T]GGCCAAGCTGGGACC | 55819 |
| rs140781484 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180059262 | CCGTCTCAGCTGAAA[C/T]ATCATTTCTTCAGGG | 55819 |
| rs140800210 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179974491 | CACAGTAAATAGTGC[A/G]ACAGAAGAGGAAAAG | 55819 |
| rs140811488 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042929 | GCTGTGTAACTATCA[A/C]AGGTGACTGAAATTC | 55819 |
| rs140845057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940849 | TACATGTATATTAAT[G/T]TTTTCATCATCTAAA | 55819 |
| rs140857369 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180022649 | TGACTGAAGGTTCCC[A/G]GGCATTCTCCTTCTC | 55819 |
| rs140882773 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179939711 | AAAGAAGAAAATCCA[C/T]TTCCAAAAGACGGAA | 55819 |
| rs140889225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180020659 | AGTAGGGCCAAGGGG[C/T]CACAGTACAGCACTT | 55819 |
| rs140913963 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966655 | AATAAAGTTTCATTC[C/T]TCCAAATACCTGTTT | 55819 |
| rs140931806 | in-del | -/AACT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953123 | CAAAAAAATATGAGA[-/AACT]ATAAATGAGTTCAGC | 55819 |
| rs140949022 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179943500 | CATGTGCACTTATTA[C/T]TTATTCAGAAAAACA | 55819 |
| rs140955419 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180024773 | CATAAAAGCCTACCG[G/T]TTTTTCATGAGTTTT | 55819 |
| rs140967920 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179960937 | AAAATTCATTAATAA[C/T]GAATAATTACAAATT | 55819 |
| rs140973474 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179982644 | ACAGTGGTGCAAACA[C/T]GGCTCACTGTAGCCT | 55819 |
| rs141069856 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180061451 | TGGTGGCTTAAAACA[A/G]CATAGTCTCATTGTC | 55819 |
| rs141118310 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179976613 | TTTTATAGATTTTCC[A/T]TTATATGTAAACTAG | 55819 |
| rs141132149 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179926237 | TTATTTATAGGCCTA[A/G]GATTTATTATTCATG | 55819 |
| rs141164790 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180005791 | CACACAGTATTTTGA[C/T]TGCATCTGTCATTGC | 55819 |
| rs141187021 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180048165 | AGAGGAAAGTGGAAA[A/G]TTACACACACAGAAG | 55819 |
| rs141289135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998595 | AGCAAAACTGTGCCT[A/T]GCTGATATCAAATCT | 55819 |
| rs141302041 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:180033563 | ACCATGGTGGTGTGC[A/G]CCTATAATCCCAGCT | 55819 |
| rs141320468 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180002036 | CTGCTTCAGCTCAGG[C/G]CCAGGGAGCATACTC | 55819 |
| rs141328628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939346 | AAATAGGGGCTCTGT[A/G]AGTTGTTTATCAATA | 55819 |
| rs141334096 | in-del | -/CAT | 0.190833 | 0.242898 | intron-variant | RNF130 | GRCh38.p7 | 5:179933280 | GATTCAATTTATTAC[-/CAT]CTAGATGTAGGAGAA | 55819 |
| rs141339319 | snp | C/T | 0.0505692 | 0.150756 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180072103 | GGAACACAAAGTCCC[C/T]CTCGCGCGGCTGCCG | 55819 |
| rs141353004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021549 | AATGTGCAAAGACAG[C/T]CTCCCTGGGTCCCCA | 55819 |
| rs141361862 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179943148 | TGCAGTGAGCTGAGA[A/T]CGCGCCACTGCACTC | 55819 |
| rs141365019 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056925 | CACAAGAAGGCATAC[C/T]GTGATTCCATGTATA | 55819 |
| rs141460505 | snp | A/G | 4.94197e-05 | 0.00497066 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966915 | AAGGGAGTTGTCGCC[A/G]GCGAGGTCGCCGAGG | 55819 |
| rs141491958 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179987945 | TTTCGTTGTGCCCTT[A/G]TCTGGTTTTAATATT | 55819 |
| rs141493322 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179945663 | ATGCTGGCTTGTGTG[C/T]TGAATGTATCGGAGG | 55819 |
| rs141498511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930097 | AGTCTTACTCTTGTC[A/G]CCCAGGCTAGAGTGC | 55819 |
| rs141504143 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179974127 | ATAAAAGGATGCAGG[A/T]TTATTAAAGGTCCCA | 55819 |
| rs141522926 | snp | A/G | 1.6489e-05 | 0.00287128 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013250 | GATGTTTTTCTCCAG[A/G]TAACTCAAAATATCC | 55819 |
| rs141528257 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928645 | TGTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC | 55819 |
| rs141535297 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180045176 | AAGATCTCATTTGCA[A/G]TGAGAGAAGGAGAAG | 55819 |
| rs141569554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996194 | AAATTTATTCCTATG[C/T]ATTTTATTCTTTTTT | 55819 |
| rs141600960 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179937848 | GGTGTAGACATACAA[C/T]GCACTGTTATTCAGC | 55819 |
| rs141612244 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179930273 | ACGTTGGTCAGGCTG[A/G]TCTCGAACTCCTGAC | 55819 |
| rs141615830 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RNF130 | GRCh38.p7 | 5:179968187 | GTACTCCCAGCTACT[C/T]GGGAGGCTGAGGCAA | 55819 |
| rs141681021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179934977 | TCGCTAGGCTTTCGA[A/G]ATTTAAGGTCGCAGA | 55819 |
| rs141720510 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180009906 | ATCCAAACCATGGGA[C/T]ATAGTTCGGCCATAA | 55819 |
| rs141774755 | in-del | -/GGAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015643 | TAGGGAAAGGAGTAG[-/GGAAAGGAGTA]GGAAAGGAGTAGGAA | 55819 |
| rs141781276 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:180027856 | CATTCACTGGGGCTC[C/T]GGCTGCCCGGCTCTG | 55819 |
| rs141788324 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179978875 | ATTCAGACACCAGAT[G/T]AATTGATTTCCTTCC | 55819 |
| rs141812144 | in-del | -/GGG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065391 | TCCCGTTTTATGGCT[-/GGG]GTGTAACACTCCACT | 55819 |
| rs141840773 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180014151 | ATGCAAGTTAATTAC[A/G]AGGACAGTCTTAAGT | 55819 |
| rs141843957 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016956 | TCAAGAAATTTAACC[C/G]TGTGTTCTTTAATAG | 55819 |
| rs141852392 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179972647 | GGACCTGGTAAAGCC[A/G]CAGCACCACCTGGGG | 55819 |
| rs141884583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950759 | AAATAATGTGAAAAG[A/C]AAGCACATTAAGTTA | 55819 |
| rs141888463 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180033970 | ATGAGAGTGGACATC[C/T]TTGGCTTGTTCCTGA | 55819 |
| rs141905691 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180019052 | TATAACCTATTATAC[A/G]TAAAGCAGAACACCA | 55819 |
| rs141908143 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179970909 | AGTGAAGAGTTCTCT[A/G]TATAGTGATTAGTTT | 55819 |
| rs141924649 | snp | A/G | 0.000264179 | 0.01149 | missense | RNF130 | GRCh38.p7 | 5:179967009 | GTACATGGCAAATTC[A/G]GCTGCAAAATATTTC | 55819 |
| rs141928491 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180038678 | GCTGCATTGATACAG[A/G]CTTCCCATCCTTTTT | 55819 |
| rs141932286 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:179999800 | GTTTTTAAAAATTTC[A/G]TTTCACCAGTTTATG | 55819 |
| rs141998983 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF130 | GRCh38.p7 | 5:179958493 | CTCTCCTCGGCCTCT[A/G]ATCCCTCCTAGGAAC | 55819 |
| rs142035700 | in-del | -/AAGA | 0.255782 | 0.249933 | intron-variant | RNF130 | GRCh38.p7 | 5:180036846 | CCCCACACTCAGCTT[-/AAGA]AATAAAACATTATAG | 55819 |
| rs142111286 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992724 | TTTTTATTTTTTATG[A/G]TTTATTTATTATTAT | 55819 |
| rs142120412 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179947835 | ATATATATACCTACA[C/T]AATATGCTATTATAT | 55819 |
| rs142152019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179931329 | AGGGACAATGGTAGT[A/G]TTTGTTTTTAATCAG | 55819 |
| rs142185021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046722 | GAGCCTCAGGATTCT[G/T]CCAAAATGTCTTCTC | 55819 |
| rs142218755 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | RNF130 | GRCh38.p7 | 5:179998119 | GCTGCGATTAGAGGC[A/G]TGAGCCACTGTGCTT | 55819 |
| rs142255823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034732 | GGGAGGATTCCCACC[A/G]TTACCTAATAAGAGT | 55819 |
| rs142276597 | in-del | -/GGAGGGATACACA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016332 | GATCTGAGGAGCTCT[-/GGAGGGATACACA]GGCCCAGTTTCACGC | 55819 |
| rs142316277 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179932814 | GCACTCCAGCCTGGG[C/T]AACAGAGTGAGACTT | 55819 |
| rs142317753 | snp | C/G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936132 | TCATCTTTCTTTTCT[C/G/T]TTATCTTGAGACAGG | 55819 |
| rs142356501 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179975603 | GTGGTGCAGTCTCAG[A/G]GAAAGTTACAGCTTG | 55819 |
| rs142456934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030258 | AAATACTTGCTTTGT[C/T]TCTCCAAGTAAGAAT | 55819 |
| rs142463632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981018 | AGGCAGGGGAGGAAC[G/T]TCAGGGAAGGTCTTG | 55819 |
| rs142538573 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180035745 | GTTCATTTTCCTTCA[A/C/G]TTGATTCTTCCCTCT | 55819 |
| rs142555565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179920643 | GGATCCCCAAGAGAC[C/T]AACCACTGGAGCTCC | 55819 |
| rs142601038 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973403 | CTGAACTCACTGTGG[C/T]CTTTTCTTCCCTTCT | 55819 |
| rs142624155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058972 | GATGGTCAATTTATA[C/T]GTTATTTTACCACAA | 55819 |
| rs142659412 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180060288 | GTTACTGCGGCAATA[A/C]GAAACTAACACACCA | 55819 |
| rs142669002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009575 | AGATGAAAACACCAA[A/G]TGCTGTCGAGAGTGT | 55819 |
| rs142671277 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:180011105 | ACAAAACGCATATAA[C/T]CTGAAACTAATCACG | 55819 |
| rs142675393 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180063429 | GATGTCATTTATTGA[A/G]ATGGGAAAGACTGGA | 55819 |
| rs142690637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960547 | TGTAGTTAGCAACCC[A/T]CCCATGACAGGGGGC | 55819 |
| rs142734510 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179995419 | TCATTTATCATTTCT[G/T]GCTGTGTGGGCCCCT | 55819 |
| rs142751135 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:180045553 | TGCCGCTGCTGGCTC[G/T]GGCAGCCTGCTTTTA | 55819 |
| rs142754326 | snp | C/G/T | 0.0130921 | 0.0798413 | intron-variant | RNF130 | GRCh38.p7 | 5:179967583 | CCTGAGGGAGAGGTA[C/G/T]AGAGCTGCTTGGGGC | 55819 |
| rs142789410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179979960 | ACCTCTGTAGGAAAA[C/T]ACAGCTAGAGTTACT | 55819 |
| rs142873566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179982509 | CATTTGCAACAGCAA[C/T]ACATGAAAATTATAG | 55819 |
| rs142876187 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180018062 | GCACTTTGGGAGATC[A/C]AGGCGATGGATCACC | 55819 |
| rs142950107 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073642 | TCTTCCATCCTCTAC[C/G]ATAGTCCTTATAAAC | 55819 |
| rs142981884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023213 | AATATCAATGCAGAT[A/G]ATTACAGATAGAAAT | 55819 |
| rs143017080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070598 | TCAGGGTGACAATGA[A/G]GGTGGGGATAATGGC | 55819 |
| rs143055899 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180040318 | GGGGAAAAAACATGC[A/T]TCCCAACAAACAAAT | 55819 |
| rs143070352 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179990917 | ATTCATATATAATCA[C/T]ATCTATGATTTACAT | 55819 |
| rs143070430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044900 | GCACAGAAGCTGACG[A/T]TAGAGGGTGCCAACA | 55819 |
| rs143070728 | in-del | -/G | 0.040671 | 0.13668 | intron-variant | RNF130 | GRCh38.p7 | 5:179952313 | CAAATGACTCAAACT[-/G]TCTCAACTATAAATA | 55819 |
| rs143105393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022756 | ACCCATTTGCAGGTT[A/G]ACTTAAGGAATACTC | 55819 |
| rs143117384 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180028180 | CCTCAACTCCGACTC[A/G]GATGCTGTTTCCTCA | 55819 |
| rs143173351 | snp | C/G | 0.000311139 | 0.0124689 | intron-variant | RNF130 | GRCh38.p7 | 5:179963427 | TCCATGTGTTTTCCT[C/G]GGATCATCTGGCACA | 55819 |
| rs143195750 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982460 | TTATTTAAGAGACTG[A/C]CAAAGTGTTTTCCAA | 55819 |
| rs143255859 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | RNF130 | GRCh38.p7 | 5:179970609 | TTTTCTTTTCCCCCT[G/T]TCAGGACATATTTTA | 55819 |
| rs143268449 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180038496 | CACTGCGACCAGCCA[A/C]AACAGGTTCTTTAAG | 55819 |
| rs143287197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031301 | AGACCAGCCCGGCCA[C/G]TATGGCGAAACCCCA | 55819 |
| rs143288630 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922899 | AGACTACACTACTGC[C/T]CTCCAGCCTGTGCTA | 55819 |
| rs143301958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989453 | TTGGGTGTATAAATA[C/T]TTTGAATTGTCATAT | 55819 |
| rs143358591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974288 | TACGTTCATCCACGC[A/G]GCAACTCCACTTCTG | 55819 |
| rs143376016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180045011 | ACCCCTGAAACTTGC[A/G]CAGCCAGGAAGGAGG | 55819 |
| rs143403692 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966120 | GATGCCTACACACAC[A/G]CTGTCAGCTCACTCA | 55819 |
| rs143471957 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RNF130 | GRCh38.p7 | 5:179968992 | TGGGGCATTACTGCC[C/T]AACTGTATACACTGA | 55819 |
| rs143510869 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180020499 | AACCTCCTGCCATGC[A/G]TCTGCTGGGAAGCCG | 55819 |
| rs143515732 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180000496 | TTTAATGCCTTTCCC[C/G]TTCTCTCCTTCTGGA | 55819 |
| rs143529580 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:180005164 | CCGGCGTGGTGGCTC[A/G]TGCCTGTAATCCCAG | 55819 |
| rs143591950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940749 | CAGTTTGATGTCTTT[C/T]GTCAGGTTTGAAAAA | 55819 |
| rs143609689 | snp | A/G | 0.029116 | 0.117091 | intron-variant | RNF130 | GRCh38.p7 | 5:179944249 | GTTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 55819 |
| rs143620921 | snp | C/T | 0.000411756 | 0.0143425 | missense | RNF130 | GRCh38.p7 | 5:179966923 | TGTCGCCGGCGAGGT[C/T]GCCGAGGGCTGATCT | 55819 |
| rs143676261 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180008200 | GACCCCAGAAAAAGC[C/T]GAGAAAAGCCCAACT | 55819 |
| rs143687854 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179994637 | GGCTTTCTCAAATGC[C/T]GGTTACAGTAGTGGT | 55819 |
| rs143706330 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179944840 | CTACCCCTGCTAGTC[C/T]CCTTTCCTCCTAATT | 55819 |
| rs143706699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966354 | GCGCAACAGGCTATG[C/T]TCCAAGAACTGTGAA | 55819 |
| rs143721554 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179950218 | CCAGGGTTCAAGCAA[C/T]AGACTCTCCTGCCTC | 55819 |
| rs143752255 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180063079 | GTAGTGAACACCTCA[C/T]ACTGCACAGAGACTT | 55819 |
| rs143778828 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179934790 | TAATGTGATCCTCCA[C/T]GCCTCAGCCTCCCGG | 55819 |
| rs143786141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180014173 | GTCTTAAGTTGCCTT[A/G]TAGTTACCTAGACCT | 55819 |
| rs143790668 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180048408 | TTAACCTCCGAATCT[A/G]GGCAATTTCTGCTTG | 55819 |
| rs143797837 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | RNF130 | GRCh38.p7 | 5:179999649 | TTGAACCCGGGAGGC[A/G]AAGGTTGCAGTGAGC | 55819 |
| rs143831100 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179943414 | TCAGGGAGGGCCTGA[C/T]GTGGACTTTCTACCT | 55819 |
| rs143873811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180056622 | GGACACGTTGGGCTT[A/G]AAAGAAGACTCAGAG | 55819 |
| rs143897464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971791 | TGCAGTTTTGATTTA[C/T]AAAAAGAGGTCTAGA | 55819 |
| rs143911354 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179925228 | GGACTTTCAGCCTCA[C/T]CCCCCAGCCTCCAGG | 55819 |
| rs143912976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180065943 | ATCTATCAAGAAAAG[A/G]TAAAAATTTTACATA | 55819 |
| rs143912988 | in-del | -/GGGGGGGG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968818 | CTGACTGTCGTGGCT[-/GGGGGGGG]GTGGTGCCATGCTAC | 55819 |
| rs143917074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179983029 | CTGTGGTGAAGTGTC[C/T]GTTCATGTGTTTTGC | 55819 |
| rs143921362 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072718 | ATGAGAGTCTAATGC[C/T]GCCCTGATCTGACAG | 55819 |
| rs144049898 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179986779 | TAAATGATCAAATAG[A/C]CTAGTATCTACATGT | 55819 |
| rs144081956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179922114 | TCACAAACACTTGAC[A/G]TGGTCAGTCTTGGAA | 55819 |
| rs144087516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975467 | CAAGGCTGAGAAATG[C/T]TGCTCTAGCTTAAAG | 55819 |
| rs144114398 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180001441 | TTACCCACATGGTCA[G/T]GATCTGTGACTGTCA | 55819 |
| rs144137107 | in-del | -/CA | 0.0299085 | 0.118574 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955218 | CAGAGAAGAAATTAT[-/CA]CAGAGTGAATGTCCC | 55819 |
| rs144147077 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180006568 | ATACCTTAAAAAGCA[C/T]ATGCATTTTCACTGG | 55819 |
| rs144172235 | snp | C/G/T | 0.00023101 | 0.010745 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040604 | TTTGATATTAGGAGG[C/G/T]ACAAAGAACCGGGTT | 55819 |
| rs144226373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180029483 | AAGGATAAAAGCTCT[A/G]ACCAAGAACCAAGAA | 55819 |
| rs144232353 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179960027 | TCAAATCTCTACTAC[A/G]CATTTGTATATGTTC | 55819 |
| rs144236298 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:180041672 | CAGTGGCAGAGGGTG[C/T]CAGCCCTGTGCCCTG | 55819 |
| rs144297382 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179964429 | ACCAATCTGACTTGC[C/T]AAAAAGTCTTAACTA | 55819 |
| rs144316977 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180052469 | GACACCACCCTTGAT[C/T]CAGAGCAGCGCCTGA | 55819 |
| rs144332547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035301 | TGTGTTATTTAGATG[C/T]GTGCTGCTTAATTTC | 55819 |
| rs144365186 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179962708 | GCATTGGATCAAAAT[A/G]GACCATAACAGTCAT | 55819 |
| rs144393566 | in-del | -/ATC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937144 | TCATCAAAACGAAAT[-/ATC]ATCAAAACGAAATAT | 55819 |
| rs144400995 | snp | A/G | 0.194902 | 0.243853 | intron-variant | RNF130 | GRCh38.p7 | 5:180062328 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 55819 |
| rs144411577 | snp | A/G | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:180013194 | CGGCTGAAGTTCTTC[A/G]GTGGCATTCGAGTTC | 55819 |
| rs144432062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179981095 | GGCGTAGGGTTAGGA[A/G]GGGGTTCCGGGTGTA | 55819 |
| rs144432124 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180034874 | AATATTCCTTTATAA[A/T]CCTTTAAGTTTCTGT | 55819 |
| rs144466347 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180010755 | GGAAGGAGGGAGGTG[A/G]CTGTGGTTATAAAAG | 55819 |
| rs144475348 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179967666 | TGGCTATTTGTTTAC[C/T]TAACAACCTTTGGTT | 55819 |
| rs144537862 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180036627 | CACTGAAATGGCTGT[A/T]TCGTCAATTTTGTCC | 55819 |
| rs144539760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065051 | AACACGCCTTTTTCA[A/G]CATTTTCCTAGTATC | 55819 |
| rs144588244 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179937702 | TCCACTGCTAGGTAT[A/G]TAACCCAAAGAATTG | 55819 |
| rs144632232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974553 | ATGAGCGGCTTGACA[A/G]CTCTGGATAGAAAGT | 55819 |
| rs144633880 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180024899 | GCAGTAAAGCTCTCC[C/T]GGGGGTGTCTGGAAG | 55819 |
| rs144667264 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:179984984 | CATTTTGGATAAAGG[A/G]TACTCAACCTATAGT | 55819 |
| rs144688723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977970 | GGGGAGTCTGGAGGC[C/T]GCGTGCCACATCGCA | 55819 |
| rs144700932 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:179942381 | GACAGATCTGTATGC[A/G]CTGATGTGGAAAAAT | 55819 |
| rs144830793 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179921031 | GATTTTAAAATTCCA[-/T]TAGTTACATTATTTG | 55819 |
| rs144891504 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:180032414 | TCTTGCTCTGTGGCT[C/T]ACCTTAGAGTGCAGT | 55819 |
| rs144897651 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:179981728 | ACTCACACTATACTA[C/T]AATTTCCCTAGGTGT | 55819 |
| rs144946808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066212 | AGGCGGTTTCCCCCA[C/T]ACTATTCTCGTGATA | 55819 |
| rs144946825 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF130 | GRCh38.p7 | 5:180013657 | TACAGCAAGAGAAGT[A/G]TATCAACATCATGGT | 55819 |
| rs144993883 | snp | C/T | 0.297636 | 0.24542 | intron-variant | RNF130 | GRCh38.p7 | 5:180057314 | AGCACTTTGGGAGGC[C/T]GAGGCGGGAGGATCA | 55819 |
| rs145028282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002268 | CAGTCCAAAGCAGCT[A/G]GGGGAAGAACAGGTG | 55819 |
| rs145030940 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF130 | GRCh38.p7 | 5:179956531 | CTTAGAGCCCATTAC[C/T]AGCTCTTTATAAGAA | 55819 |
| rs145058472 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179965379 | GGTTTAGTTCAATCA[C/T]GTGGGTTTTATTTAT | 55819 |
| rs145059048 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179997069 | TCTGGGAAAATTTAC[C/T]AGTGGTTGTCAATTT | 55819 |
| rs145064120 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180046351 | ACCAAGGCGAGGAGG[C/T]ACCGAGAGCGAGCAG | 55819 |
| rs145064746 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179961399 | TTGAACTAAGTAAGG[C/T]ATGGATCTAAGATCC | 55819 |
| rs145121377 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179954269 | AAGAGAACTGAAAAT[A/C]TATGTTCAGGCCAAA | 55819 |
| rs145273656 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | RNF130 | GRCh38.p7 | 5:180042600 | GCAGCTCAGTGACCT[C/G]TTACGATAATCTCCT | 55819 |
| rs145286846 | in-del | -/CT | 0.0513262 | 0.151752 | intron-variant | RNF130 | GRCh38.p7 | 5:179946984 | TTGGCAAATAAAGTA[-/CT]CTCCTTACAGGATCT | 55819 |
| rs145288544 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179978468 | ATTATGTCTAAGTCA[A/G]TCTATTTTGTTTTAA | 55819 |
| rs145292138 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180063284 | ACTAAGGCGGCAGCC[A/G]TGAAAATGTCAAACA | 55819 |
| rs145299309 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179981720 | TATCCAATACTCACA[A/C]TATACTACAATTTCC | 55819 |
| rs145301223 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179935872 | CTCCTTCCTGGACAA[C/T]GCAAGCATGTTAGAG | 55819 |
| rs145303746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069499 | AAGGGAGGCTAAAAC[C/T]CAAGGGGACTGACTT | 55819 |
| rs145338756 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935525 | AGCACGTGTGTGTGT[-/TG]GTGTGTGTATACATT | 55819 |
| rs145343464 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:180068264 | CTAGCTAGGCTGCTC[C/T]GCAAAGGTACTAAAT | 55819 |
| rs145363479 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179939382 | GGTACAATTCTACCA[A/G]TAGTTGAGTTCATTT | 55819 |
| rs145377805 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:179938239 | CTGGGATCACAGGCA[C/T]GAGTCACCGCGCCCA | 55819 |
| rs145377859 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976314 | TTCTAGTAATATACC[A/C]ATGAATGGTTTTGGA | 55819 |
| rs145382037 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180061361 | TGCTGGCAAAGCTAA[A/C]CCTGCATGCCTGTGT | 55819 |
| rs145441798 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932419 | TGCGCCACCACTCCC[A/G]GCTGATTTTTCTGTA | 55819 |
| rs145442066 | snp | A/T | 6.59022e-05 | 0.00573993 | intron-variant | RNF130 | GRCh38.p7 | 5:179980119 | TGCTGAAGTTGTTTC[A/T]TGACTGTACCTTGTC | 55819 |
| rs145453915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987640 | CATGTGTATCTTTCA[C/T]TATATTGAAGTATGT | 55819 |
| rs145602523 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180001373 | ATGGGACCATGTCCT[A/G]GGCTCAGAGTCTCAC | 55819 |
| rs145652271 | snp | A/G | 3.29815e-05 | 0.00406075 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179978271 | TGCACAATGATCAAA[A/G]TCTGGGTCAGTTTCC | 55819 |
| rs145655726 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:179961947 | CACTGTGCTAAGCAT[C/T]TTATAGGCTGATTCT | 55819 |
| rs145662897 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:180044420 | ACTTATTTACCTCTT[A/G]ACAGGCACCAAACAA | 55819 |
| rs145679857 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:179974207 | ATGGACCCTCGGCTG[C/T]AGTGGAGCCTCAGAC | 55819 |
| rs145687804 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:180058309 | TTTTCAGTGTATGTT[A/C]CAGCTGGTAAAAATG | 55819 |
| rs145715073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058106 | AGTTAAGGAACAGGT[A/G]TAAACTACGGTGTCA | 55819 |
| rs145743560 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179927931 | TAAATGGAAACAGGG[A/G]ATATATTCTTTTGTG | 55819 |
| rs145748392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007357 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 55819 |
| rs145776987 | snp | A/C | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 5:180043804 | CAAAATTCATCTAAT[A/C]ATCATCCATAAAAGG | 55819 |
| rs145821074 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180062513 | CAACATTGAGACTAC[A/G]GCACCTACTACACCC | 55819 |
| rs145846423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933306 | GAGAATTTAGGTGTC[C/T]TATTTCTTCCTGTAT | 55819 |
| rs145846693 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015607 | GTAGGGAAAGGAGTA[-/G]GGAAAGGAGTAGGGA | 55819 |
| rs145905584 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034591 | TATTTTTAGGAATTT[G/T]TTCATCTAAGGTGTC | 55819 |
| rs145934409 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015049 | CCAATGGAACATATA[C/T]CTTTTTACTACCTTA | 55819 |
| rs145996183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057539 | GGTGACAGAGCGAAA[A/C]TCAGTCTCAAAAAAA | 55819 |
| rs146000548 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180060595 | CACTTGCCAGCACTT[C/T]CACCCTAACTTAGCG | 55819 |
| rs146012504 | in-del | -/GCAATCTCGACTCACT | 0.259674 | 0.249813 | intron-variant | RNF130 | GRCh38.p7 | 5:180021042 | CTGGAGTGCAGTGGC[-/GCAATCTCGACTCACT]GCAATCTCTGCCTCG | 55819 |
| rs146018782 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179931068 | AAAAATCAAGAATAG[A/G]TGTTGAATTTTAGCA | 55819 |
| rs146020692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011138 | GGAACACAACACGTC[A/G]GATAAACTCAAATAC | 55819 |
| rs146021859 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179945014 | GGTGGGGTGGCTCAC[G/T]CCTATAATCCCAGCC | 55819 |
| rs146052492 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180027882 | CTCTGTGGCTGCTGC[C/T]GGTGTGAGACTGCAC | 55819 |
| rs146053234 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179995420 | CATTTATCATTTCTG[A/C/G]CTGTGTGGGCCCCTT | 55819 |
| rs146070063 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180032928 | ACTGCCACCCTGACA[A/G]TACTGAACAATGGAA | 55819 |
| rs146142560 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179991102 | TTTCTCCTTTTAGCA[C/T]TTTGAAAATAGCATC | 55819 |
| rs146149054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179949256 | CAGGCATGAGCCACC[A/G]TGCCCAGACAATTTT | 55819 |
| rs146177315 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180059920 | AGGGGGAACTAGGTT[A/G]CAGATGAAACAAGGT | 55819 |
| rs146192465 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF130 | GRCh38.p7 | 5:179930277 | TGGTCAGGCTGATCT[C/T]GAACTCCTGACCTCG | 55819 |
| rs146245696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051902 | CATGCAAGATGCTAC[A/G]GATCTAAATAACTGA | 55819 |
| rs146260242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973313 | CTCCACAGGCAGCTG[C/T]CCTGAACACGGCACC | 55819 |
| rs146264367 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | RNF130 | GRCh38.p7 | 5:180057123 | TGGAAGATGGGGTCT[C/G]GTTGCCAGAGGAACC | 55819 |
| rs146279609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926258 | ATTATTCATGTGCCC[A/G]ACTACAGCCATCATG | 55819 |
| rs146295685 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180038902 | AGTAAAGAAGAAATC[A/G]GCATGGAATGAAGAT | 55819 |
| rs146348005 | in-del | -/CT | 0.203575 | 0.245652 | intron-variant | RNF130 | GRCh38.p7 | 5:179995201 | CAGTATGGGACCTGC[-/CT]CCTCTCTCTCTCTCT | 55819 |
| rs146382897 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179952097 | TACCACTTTGGGAGG[C/G]TGAGGTAGGAGGATT | 55819 |
| rs146399233 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179956922 | ATGAATGAGGGGGCG[C/T]TGTCAACTTTTTTGA | 55819 |
| rs146445313 | in-del | -/CTAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953121 | CACAAAAAAATATGA[-/CTAA]GAATAAATGAGTTCA | 55819 |
| rs146463476 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180020623 | TTCTTCCTTGAACAG[C/G]AAGTTCTTCAATCAC | 55819 |
| rs146479689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179922270 | GAAGTGTTTTGTTCA[A/G]ATCTTTAGTCCATTA | 55819 |
| rs146483035 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:180001793 | GGGAGGATAGCACAG[C/T]GATAATTCCACTCTC | 55819 |
| rs146485899 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007060 | GTTATTTACAATATA[C/T]GGATCTCTTTGGTAG | 55819 |
| rs146500468 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:179926848 | TCACCCTGGGGGACC[A/T]GATGCCATTTCCAGG | 55819 |
| rs146512312 | in-del | -/AACT | 0.496937 | 0.0390173 | intron-variant | RNF130 | GRCh38.p7 | 5:179953122 | ACAAAAAAATATGAG[-/AACT]AATAAATGAGTTCAG | 55819 |
| rs146551170 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180048137 | TCAGGTCAACAGCAT[G/T]CTAAGAATCGGGAGA | 55819 |
| rs146584759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053070 | AGCACTCAAGAACAC[C/T]TCTGAGAGGCAGAAA | 55819 |
| rs146596862 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003695 | AGCCACTATTTTTTT[-/T]AAAATTTTTCATTCT | 55819 |
| rs146607900 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179986486 | ACTATGTGAGAACCA[C/T]AAGAGGTCACTTTTA | 55819 |
| rs146668301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025379 | AAGCACAGAAAAGAC[A/G]AAAAAGTAAATCAAG | 55819 |
| rs146687161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031532 | AAAAGTTATACGTAG[C/T]TTTTTGACTGTGTGG | 55819 |
| rs146696625 | in-del | -/AGGAATCACAAAACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977426 | GTTTTTGAAACCCAC[-/AGGAATCACAAAACA]ATGCCAAGCACAGTG | 55819 |
| rs146722727 | in-del | -/A | 0.0448719 | 0.142907 | intron-variant | RNF130 | GRCh38.p7 | 5:179953741 | AAAGTACAATCAACC[-/A]AAGGAAAAATAAACA | 55819 |
| rs146723421 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180056071 | CCTGGGCGACAGAGC[A/G]AAACTGGGTCTTAAA | 55819 |
| rs146739838 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179969002 | CTGCCCAACTGTATA[C/T]ACTGAAACTGTGTTT | 55819 |
| rs146742845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179921311 | CCAGGGAAACATAGA[C/T]TAGTTTGCATCTTTC | 55819 |
| rs146843282 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179943462 | TTTAAACTGTAATCA[G/T]TTTTACTATTTTTAT | 55819 |
| rs146844835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180024698 | GGAAATGACACCAAA[C/T]GGAAACTTGGAAATT | 55819 |
| rs146848915 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180030520 | CGTTTTTAAAAATAC[A/G]TGTTCCCTTTTTGGT | 55819 |
| rs146856245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180059194 | GTGTATATTTCCTTG[A/G]ACTGAAACATCCTCC | 55819 |
| rs146856384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003726 | AAGTCTATTTGCATC[C/T]GGCTAACTCTCAAGT | 55819 |
| rs146862442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179947054 | ACAAGTGCACACTGA[C/T]GCAACCCTACTGTAC | 55819 |
| rs146879255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009639 | GAATGCAAAATGGTA[C/T]GGCCACTTTGCAAAA | 55819 |
| rs146902980 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179929280 | GTGTCTGTACATGCA[C/T]GGCTGTTTCAGAACT | 55819 |
| rs146903340 | in-del | -/GGAAAGGAGTAG | 0.497091 | 0.0380279 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015746 | GTAGGAAAAGGAGTA[-/GGAAAGGAGTAG]GGAAAGGAGTAGGGA | 55819 |
| rs146906113 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179932815 | CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTTG | 55819 |
| rs146994921 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180037728 | TGGAGTGAAATTAAT[G/T]ATCGCAGTGTGCAGA | 55819 |
| rs146998490 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987992 | GGTAGAATGAGTTAG[A/T]AAGAATTCTCTCTTC | 55819 |
| rs147048818 | in-del | -/GTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983143 | CTCACTTTATGGCAG[-/GTTT]TTTTTAATTTGATGA | 55819 |
| rs147082561 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:180010425 | AGTGCAGTGGTACGA[A/T]CATGGCTCACTGCAG | 55819 |
| rs147099049 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179967388 | TTGAAGAATCCCAGG[C/T]AATAGAAAACACCTC | 55819 |
| rs147102460 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179971110 | GATGGGAGATTTTCT[C/T]TCTTATTCAGGCAAG | 55819 |
| rs147104389 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180055482 | TGTGCGCGCGCGCAC[A/G]CGTATGTGTCTGTGT | 55819 |
| rs147118364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923164 | CATCTAGAAGCTTTA[C/T]AGTTTTAGTTCTCAC | 55819 |
| rs147152455 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001245 | CCTACTATTCTTGCT[G/T]TCCCCACAATGAGGA | 55819 |
| rs147155552 | snp | A/G/T | 0.000148258 | 0.00860863 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040529 | TGCATTGTGGAAAGC[A/G/T]GCCCGTGATATTTTC | 55819 |
| rs147155569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959514 | GTGCCTGTAATCCCA[A/G]CTACTCAGAAGACTG | 55819 |
| rs147157274 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180005447 | AAAACAACAACAACA[A/C]CACCAACAGAAACCA | 55819 |
| rs147188634 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180021918 | ATGCTACACTCAGTC[A/G]TCACGTCATAGCCAT | 55819 |
| rs147246695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066029 | GTGTCATCCTAATAA[C/T]GTTTAATGTTTTCAC | 55819 |
| rs147258638 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179980378 | GATTCAGCATTCTGG[G/T]TGAAAAGTAAAAAGT | 55819 |
| rs147264258 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072778 | CACCTCCTGCTCGCT[C/T]ACTGGTTCCTCGAAG | 55819 |
| rs147277786 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179940766 | TCAGGTTTGAAAAAT[A/T]GTGTCATTATCTCTT | 55819 |
| rs147293764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999898 | TATCAATTTTTAATT[A/G]CCTCTGGTTGTTTTA | 55819 |
| rs147308748 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179923823 | TTCCCTAAAGTTTTT[A/C]TTTTAACAACACTAA | 55819 |
| rs147370319 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180048644 | TGCTATCTCAAAAAC[A/G]GGAAGAGGGAATTTA | 55819 |
| rs147385087 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920172 | TTGGGGGAACTTTGC[A/G]AATTAACCCTGAACC | 55819 |
| rs147398424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979975 | CACAGCTAGAGTTAC[C/T]GTAAGAAGGTAGTTT | 55819 |
| rs147474022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028242 | TCACTTCCCACAGTC[A/C]TGACTTCGTACTCAA | 55819 |
| rs147474880 | in-del | -/CAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931779 | ACTCTGTCTTAAAAC[-/CAAA]AAACAAACAACAAAA | 55819 |
| rs147504710 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179964061 | CGAGCCGGCCTCCCA[C/T]GGCATCCATGGCTAC | 55819 |
| rs147558029 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179948864 | AGACTGCCTTAAGCT[G/T]CTGGGTAGAATCAGG | 55819 |
| rs147574375 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179954292 | AGGCCAAAATTTGTA[A/C]ATGAATGTTCACAGC | 55819 |
| rs147663879 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179928419 | CACTATGTTTTAACG[A/T]CCATTCCCCAAATGA | 55819 |
| rs147665307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061419 | TTTCCAGTGGCGGCC[A/G]CAAGACATCACAAAC | 55819 |
| rs147680294 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:179932648 | ATCAAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 55819 |
| rs147738606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974267 | TCCTGAAGTGGCATG[A/G]AAACATACGTTCATC | 55819 |
| rs147752621 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180058528 | TGCGGCAGAGGGGGT[A/G]ATGGAGTCTTGTCAT | 55819 |
| rs147769603 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180041855 | GCCGAGGCAGGTAGA[C/T]TGCTTGAGCCCAGGA | 55819 |
| rs147841062 | snp | A/C | 1.64999e-05 | 0.00287222 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966873 | AGGAAGAGGTGAGAT[A/C]CCCGAAGTTCGAAGT | 55819 |
| rs147843067 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179955041 | TAATTAGATGTGGTT[C/T]GGAAAATCATTTTGA | 55819 |
| rs147857163 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180036825 | AAGAATATAATGTCT[C/G]TCTACCCCCACACTC | 55819 |
| rs147873876 | snp | C/G/T | 0.00239401 | 0.0345304 | intron-variant | RNF130 | GRCh38.p7 | 5:180018711 | TGCCCATTCTCTCTT[C/G/T]GCCCCCTGCCCACTG | 55819 |
| rs147874398 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:179970868 | ATAGAAAAATGGAGT[C/T]TCAAAAAGATACTAA | 55819 |
| rs147877873 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973636 | CGCACGCCTGACCGC[A/G]CTCACCCTCACTATG | 55819 |
| rs147980510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978515 | TATTAATTTTGTTAT[C/G]ATATGTCTTACAAAA | 55819 |
| rs148069157 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | RNF130 | GRCh38.p7 | 5:180026733 | AGGTATAAAACATAG[C/G]CTTAAATGAAAAGAA | 55819 |
| rs148121448 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179950624 | TGACAAATGTTCCCT[A/C]AGACTGATGGGAAGT | 55819 |
| rs148135674 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934840 | ACAGGCATGAGCTAC[A/C/T]ATGCTCGGCTTGGTT | 55819 |
| rs148138793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180014612 | AAATATTTGGTTTTA[C/T]ATGTTTCATTTACCA | 55819 |
| rs148145075 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:179999670 | TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC | 55819 |
| rs148182690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056887 | TTCATCTCACTAACA[C/T]GATGTGAGCAAAAGA | 55819 |
| rs148191557 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179940260 | TTGAGTTGGAGTCTC[A/G]CTCTGTCACCCAGGC | 55819 |
| rs148279699 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179982507 | TACATTTGCAACAGC[A/C]ATACATGAAAATTAT | 55819 |
| rs148281907 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180071251 | AAGTCTTTTTTAAAA[G/T]AAGGGAAAAACCCAG | 55819 |
| rs148300173 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179922927 | CTACAGAAAAAAAAA[A/T]AATAATAATAATCCT | 55819 |
| rs148347832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974454 | GGAGGAGGCCCCTCC[A/G]CCATGCCAACTGCCA | 55819 |
| rs148350428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059210 | ACTGAAACATCCTCC[C/T]TTCTGCCCCCTCTCA | 55819 |
| rs148351282 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179929466 | TAAATTCTAGGATCA[C/G]GCTGGGCGTGGTGGC | 55819 |
| rs148355889 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180045112 | TAAGTAAGACGATAT[A/G]TAACAGAGCCTACAA | 55819 |
| rs148437710 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179954232 | AACATAATCCAGCAA[C/G]TGCACTCCTAGGGAC | 55819 |
| rs148441144 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180035713 | TCTGACAGTGTCCCA[C/T]AGGCATCTGAGGCTC | 55819 |
| rs148463725 | in-del | -/TGCCTTGCAGGT | 0.25634 | 0.24992 | intron-variant | RNF130 | GRCh38.p7 | 5:179999107 | ACTCACTGCAGCCTC[-/TGCCTTGCAGGT]TGCCTTGCAGGTTCA | 55819 |
| rs148475832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001439 | TGTTACCCACATGGT[C/G]AGGATCTGTGACTGT | 55819 |
| rs148507073 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | RNF130 | GRCh38.p7 | 5:179942482 | CTTAGTCTCGAATTT[A/C]AGTAACTGTTTTTGG | 55819 |
| rs148548615 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179947533 | CTGGGGGCCAGCTTA[C/T]GTGTTGAAATCCAGC | 55819 |
| rs148597231 | snp | A/C/T | 0.040671 | 0.13668 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073413 | TTAGTCGTGGTGATG[A/C/T]GTGCCTGTAGTCCCA | 55819 |
| rs148613518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925611 | CTAGCTCACTGCAGC[A/G]TCAACCTCCTGGGCT | 55819 |
| rs148617446 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180005577 | CTCCTGCCCACTATT[C/T]CTGATGTTTCAGTCA | 55819 |
| rs148652323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179975546 | GATAACTGCACTGTC[A/G]CTACATGGCAGTGAG | 55819 |
| rs148654270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060604 | GCACTTCCACCCTAA[C/T]TTAGCGCAGGGATTC | 55819 |
| rs148685211 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180046492 | GAAGCACTCACCATG[C/T]TGTGTAGGCTAAGGG | 55819 |
| rs148705406 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179980619 | TAGGTGTGTAAATGC[C/T]GTCTTATTAAGGGAA | 55819 |
| rs148769235 | snp | A/G | 0.00139969 | 0.0264176 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013232 | TATTGTCATTTGTAC[A/G]GAGATGTTTTTCTCC | 55819 |
| rs148785132 | in-del | -/C | 0.0252325 | 0.109451 | intron-variant | RNF130 | GRCh38.p7 | 5:179929789 | GGTCCAGTTTCAATA[-/C]ACACACCCACACCCA | 55819 |
| rs148815122 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180025641 | TTATGAATTTTTTTT[A/T]AAAAAATGTATGAAC | 55819 |
| rs148865564 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939958 | AAACGTCCCTTTTTT[-/T]TTTTTTCTAGCATCA | 55819 |
| rs148913957 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179960199 | GAAATTCAGTAACCT[C/T]GCTTACCTAGGTACT | 55819 |
| rs148920713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180058167 | GAGGAGGGAAGGAGC[C/T]GTGACTGGAAGGGAC | 55819 |
| rs148935319 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179928346 | TTTCTGTGCCAATAA[C/T]GGATATTTTGTTTTT | 55819 |
| rs148949811 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007613 | AACCTTGGGGAAAAC[A/G/T]GAAGGAGGAAAAAAG | 55819 |
| rs148967430 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994386 | GTCCTCTTTTATTTC[A/G]TTGAGCAGTGGTTTG | 55819 |
| rs148970164 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179977710 | TACAAAAATTATCTG[A/G]GCATGGTGGTGGGTA | 55819 |
| rs148973604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063039 | CCTGGGGGTGGGGAG[A/G]AGGAAGGGGCTGGAG | 55819 |
| rs148996648 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041543 | TTAAGAAGAAGCCCC[C/T]GGCTGCTCTTCCCAC | 55819 |
| rs149023737 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179981817 | GCGTGTGGCTGCTCC[A/G]TCTTTGAAGCCTAAT | 55819 |
| rs149112564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180032881 | TTGCATAGGTACATA[C/T]CACAAGGAATTTATA | 55819 |
| rs149122811 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179997933 | TGCAACCTTTGCCTC[C/T]TGGGTTCAAGCAATT | 55819 |
| rs149144198 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | RNF130 | GRCh38.p7 | 5:179970595 | AATTTTTAGTTAAGT[C/T]TTCTTTTCCCCCTTT | 55819 |
| rs149160014 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180053433 | GAAAGAAAATGACAC[A/G]TTTTATGAAGAAAGC | 55819 |
| rs149178009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956125 | CCTCCAGACCTTGTG[G/T]GTGTTTCTGTCCTTG | 55819 |
| rs149181675 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180019765 | AGTTTTCCTAAAATA[C/T]AGACCTGCTGTCACT | 55819 |
| rs149252293 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059794 | GAAAGCTGTAATGGT[A/C/G]GGGTGCCAGCACAGG | 55819 |
| rs149268292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010671 | GGCCCATGATTCCAC[C/G]TATTTAACATTCTTG | 55819 |
| rs149268775 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038520 | CTTTAAGACTTCTCA[A/G]AGACCCAAAAATGTT | 55819 |
| rs149288829 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179949610 | AATTTTAATCTCGAA[G/T]TTTTTAAATAGTAAA | 55819 |
| rs149305947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180064592 | CTTACTCTTCATCTC[C/T]CCTTCTTCCCAATTT | 55819 |
| rs149320317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936586 | GCAGATATTTTTCCT[C/T]CCAATACTTTACTAT | 55819 |
| rs149343362 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179984383 | AAAAAGAATTTAGTC[A/G]TTCACCATTAAATAT | 55819 |
| rs149427846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048346 | TTCCAGGTTGCTCTG[C/T]CCTGCTTCTAGGCTA | 55819 |
| rs149430993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999464 | TGGTGGCTTACGCCT[C/G]TAATCCCAGCACTTT | 55819 |
| rs149481905 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180056584 | ACTAGAGGAGGAAAA[G/T]ATTAGGAAAGATGAA | 55819 |
| rs149517459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021875 | CTTTCCCAATAACGT[C/G]CTTTACAGCAGCCCA | 55819 |
| rs149534138 | snp | A/G/T | 0.00358891 | 0.0422285 | intron-variant | RNF130 | GRCh38.p7 | 5:179975190 | AAAGACAATAGGGGC[A/G/T]GGGAGGCGTCCCAAG | 55819 |
| rs149554963 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015548 | AGTAGGAAAGGAGTA[-/G]GGGAAGGAGTAGGGA | 55819 |
| rs149570484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180029042 | CAGTTTAAGGACTCC[A/G]TTACCCGAAATCACA | 55819 |
| rs149610075 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928283 | TGTTCCAAAGTGGCT[-/G]GTGCCAACTTTGACT | 55819 |
| rs149635785 | snp | A/C | 3.30169e-05 | 0.00406293 | missense | RNF130 | GRCh38.p7 | 5:180013089 | CGTGCATTTGTGTAC[A/C]TGATCTTCTGAATGA | 55819 |
| rs149636659 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003607 | CCCATCACTTTGCGA[C/G]AGGTAAACCTGTGAC | 55819 |
| rs149652324 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179962487 | ATATGGAGATCACGT[A/G]AATTCCACCCATATC | 55819 |
| rs149695896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996579 | CATTACCACATGGTT[C/T]TTGTTCTTCATTCTG | 55819 |
| rs149740298 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000591 | TTTCATTCTTATTTC[-/T]TTTTTTTTTGTCTCT | 55819 |
| rs149745382 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179921217 | CGACACCACCATCAA[G/T]ATAACGAACATATCC | 55819 |
| rs149749329 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001314 | TGTTACCCACAAGCA[G/T]CTGCAGCAGCACTGG | 55819 |
| rs149794023 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179940911 | ATTTTATTTTTTTGC[G/T]TCAGCTCAGATAGTC | 55819 |
| rs149797906 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179973572 | GGCCAAGGCTGAGCA[C/T]CTGCAGGGCCATCAC | 55819 |
| rs149832126 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179991808 | AAATCACCATAACGT[A/C]GAATCAGTAGGAGCC | 55819 |
| rs149834990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023857 | TGCACAGTGGTGTCA[A/G]AAGTTATCATATGGC | 55819 |
| rs149850291 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179977000 | ACCAACATGCTGTTT[C/G]CAGGGCAACCAGGCA | 55819 |
| rs149888792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031869 | TTCACATTTCTACTC[A/G]CAATACATAAGGATT | 55819 |
| rs149908184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041114 | GGCCAGTGAGGAGGC[C/T]AAAATAATCCTCGGT | 55819 |
| rs149911423 | in-del | -/TCTC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000818 | ACACGTTTTCTTGTA[-/TCTC]TCTGAGTTTCCATAC | 55819 |
| rs149961590 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF130 | GRCh38.p7 | 5:180046161 | GCTGAGGGACCCAGC[A/G]CACCCTCCGCAGCTG | 55819 |
| rs150009147 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012196 | CCATGCCAAAGTCTG[C/T]GCTTTTTCCGCTAGA | 55819 |
| rs150027697 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | RNF130 | GRCh38.p7 | 5:179953229 | CCATGCTCATGAGTT[A/G]GAAGACAATATTGTT | 55819 |
| rs150045670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068121 | TCTTCCCCACCAGCA[C/T]ATCTGCATACATAAT | 55819 |
| rs150049084 | snp | G/T | 0.410399 | 0.191761 | intron-variant | RNF130 | GRCh38.p7 | 5:180019251 | TAGCCGGGCGTGGTG[G/T]CGGGCACCTGTAGTC | 55819 |
| rs150096346 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179987621 | TATGATGTTAGCTGT[A/G]GGTCATGTGTATCTT | 55819 |
| rs150104980 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180059596 | CATGCAAATGAGAAG[A/G]TGCATCACTGACCTT | 55819 |
| rs150114254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943552 | GAAGAAAAAGGGGAT[A/G]AAGAGGAAAAGGCGT | 55819 |
| rs150149931 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | RNF130 | GRCh38.p7 | 5:179994162 | AGTCAGGTAGCATGA[C/T]GCCTCCAGTTTTGTT | 55819 |
| rs150158538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180063995 | CACAATCACACTGTG[C/T]CCAATTCCATTACCG | 55819 |
| rs150186685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048294 | GGGAGTCTGTAGTCC[A/G]GTTTACGGCAAATCA | 55819 |
| rs150207439 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966927 | GCCGGCGAGGTCGCC[A/G]AGGGCTGATCTTCGG | 55819 |
| rs150225056 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180043375 | TTAAAAAACACTCTT[G/T]CCCTTTGTTTGTTTC | 55819 |
| rs150275155 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:179966739 | GAGTGCCTTGACTCT[C/T]CTGATGGTCCCGAAT | 55819 |
| rs150330043 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179971463 | CAAGCTCCGCCTCCC[A/G]GGTTCACACCATTCT | 55819 |
| rs150365642 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180021793 | ACATAATACAACCCC[C/T]AAATAAGGAGCTTAA | 55819 |
| rs150399439 | in-del | -/GC | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072929 | CGAAACGCGCGCGCG[-/GC]CGCACACACACACGA | 55819 |
| rs150434843 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179998496 | AGAAACGCCATCTCA[C/T]TATATTGCCCAGGCT | 55819 |
| rs150489243 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180003005 | GATCAGAATTCTACC[A/G]AAGAGTTCTGAACAG | 55819 |
| rs150538523 | in-del | -/GGAAAGGAGTAGGGAAAGGAGTAGGAAAGGAGTAGGAAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015701 | GTAGGAAAGGAGTAG[lengthTooLong]GGAAAGGAGTAGGGA | 55819 |
| rs150577897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179979341 | AAGGCAACTAGATAC[A/G]GTGGTATCAAGGCAA | 55819 |
| rs150628000 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF130 | GRCh38.p7 | 5:180034037 | TATGATGCTAACTGT[A/G]GCTTTTCCACAGATG | 55819 |
| rs150631083 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:179984243 | GACAGCTTACTTCTC[A/C]ATTTCCACAATGGAT | 55819 |
| rs150632308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180018203 | GGGAGGCTGAGGCAG[A/G]AGAATTGCTTGAACA | 55819 |
| rs150667694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040376 | ATTACATGGCTTCAG[C/G]AGAGGCAGAATGCTT | 55819 |
| rs150668964 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073747 | GCGGGGTCCTCGCCC[C/T]GGGCCTGGCACCTAA | 55819 |
| rs150677242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958919 | CTCCTGACCTCAGGT[A/G]ATCTGCCCACCTCAG | 55819 |
| rs150714530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180006126 | CAGCTCAAACATCTA[C/T]TTCCCCTTTCCAGTT | 55819 |
| rs150731434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964499 | TAACAAAATGTTATA[C/T]AATAAAATTACCTAT | 55819 |
| rs150768080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012094 | CTTTCAGATGAGAAA[A/G]AAGCTGAGATGCTCA | 55819 |
| rs150786265 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179940379 | GTGCCCGGCACCACA[C/T]CCAACTAATTTTTAT | 55819 |
| rs150835403 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179990271 | GTCACGTGAGTCACA[C/T]GTCCACTGGACAGGG | 55819 |
| rs150838580 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF130 | GRCh38.p7 | 5:179946011 | AGAAGCATATGACTG[A/G]CGTTCCTTCAGCAAG | 55819 |
| rs150844475 | snp | C/G/T | 0.0291275 | 0.117185 | intron-variant | RNF130 | GRCh38.p7 | 5:180060997 | TGGCGTGAACCCCGG[C/G/T]GGGGCGGAGCCTGCA | 55819 |
| rs150873166 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:180045304 | TCTTGCTGACTTCAA[A/G]AAGGAAGCCGCGGAC | 55819 |
| rs150889714 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179996379 | AGAAGTGGTGAAAGT[A/G]GGCATCCTGTGTTTT | 55819 |
| rs150904791 | in-del | -/AAG | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179952427 | GCTTCCAAATATCTA[-/AAG]AAGAATTAACACAAT | 55819 |
| rs150949727 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179987054 | AGTTTTTGGTGAACT[A/C]TTTGTTTTTTTTCTA | 55819 |
| rs150979805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973409 | TCACTGTGGCCTTTT[C/G]TTCCCTTCTAGGCAA | 55819 |
| rs150981496 | snp | A/G | 0.000280008 | 0.011829 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966924 | GTCGCCGGCGAGGTC[A/G]CCGAGGGCTGATCTT | 55819 |
| rs150985218 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179960916 | CAGAAATAAAATAGA[C/T]GTTGAAAAATTCATT | 55819 |
| rs150986980 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042840 | CGCATACATGCACAA[C/T]GTAGTAAAAAGCAAA | 55819 |
| rs151034307 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF130 | GRCh38.p7 | 5:180008980 | GAAGTCTCAAAAGAA[A/G]AAAATACATAGGACT | 55819 |
| rs151108265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023413 | GAGAAATGGCTGATT[C/G]TAGGACTGATGTGTC | 55819 |
| rs151159725 | snp | A/C | 0.0667028 | 0.170006 | intron-variant | RNF130 | GRCh38.p7 | 5:179948414 | TTGGCTCATGCCTGT[A/C]ATCCCAGCACTTTGG | 55819 |
| rs151190543 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | RNF130 | GRCh38.p7 | 5:179932321 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGA | 55819 |
| rs151198009 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179998258 | CTGCTTTTGCTGTAT[C/T]CCATAGGTTTTGGTA | 55819 |
| rs151247772 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180053953 | TCCTGCTTTAGCCTC[C/T]CGAGTAGCTGGGACT | 55819 |
| rs151251309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002916 | AAGGTAACTCAGATC[C/T]GGGTTGTTATTATTA | 55819 |
| rs151317550 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:179981024 | GGGAGGAACGTCAGG[C/G]AAGGTCTTGAGGAGT | 55819 |
| rs180773288 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179935719 | GTTTTCTCTCTATTA[A/G]TGTATTATATTATTA | 55819 |
| rs180788003 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954609 | TTTTTTACGGGGTGA[A/T]GAAAATGTTCTGGAA | 55819 |
| rs180796135 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023083 | GTAGGATGGCAAGAG[C/G]CAGGTTTTTCATTTA | 55819 |
| rs180797059 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969645 | GGCTGAGGCAGGAGG[A/G]TCACTTGAGGCCAGG | 55819 |
| rs180801033 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976887 | CAAACTCTTTGGTTT[C/T]AGGCTTCTTGGCAGG | 55819 |
| rs180808548 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179927751 | GCCACCACGCCTGGC[C/T]AATTTTTTTTTTGTA | 55819 |
| rs180810369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179963843 | CCACCAAAAAGTGTG[C/T]GGTGAAAATATGTAT | 55819 |
| rs180811144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986328 | CCTCTATCTATGGTA[C/T]AAATCAAGCAATACA | 55819 |
| rs180832889 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034472 | ATTTGATAGACTGCA[C/T]CAGCGAATTTCATGG | 55819 |
| rs180837333 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004877 | AAATCTTTCCCCAAT[A/G]CAAAGTGCCTTGTAG | 55819 |
| rs180844473 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179946944 | CACCCTAGCTCCCGT[C/T]ATTTCTACCTGTTTT | 55819 |
| rs180849207 | snp | C/T | 0.00110088 | 0.0234356 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015399 | CACACCAGGTACAAA[C/T]GGTTTTAGAAATCAG | 55819 |
| rs180853438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996430 | TTTTCAGCTTTTCCA[C/T]GTTCAGTATGATGTT | 55819 |
| rs180875185 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180057310 | TCCCAGCACTTTGGG[A/T]GGCCGAGGCGGGAGG | 55819 |
| rs180891405 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039611 | GTGGGGAAGTACCAA[A/C/T]GACTCTCAATTAAGG | 55819 |
| rs180892607 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052151 | CCCAGGCCCTCTTTT[C/G]TCAGTGGACAGTATC | 55819 |
| rs180895033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973451 | AACAGTCTGGTGCTC[A/G]GCAAACCACCTTTCT | 55819 |
| rs180898103 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180019309 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 55819 |
| rs180899367 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990906 | TGATTAATGATATTC[A/T]TATATAATCATATCT | 55819 |
| rs180900476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011320 | AGGTCTATCAATCAG[A/G]TAATGTATTATATCA | 55819 |
| rs180902713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959112 | TTGAGTATTAAACCA[A/G]GCAATACGGGTAAAA | 55819 |
| rs180912145 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060549 | CCAGCAGCCTAGATT[G/T]TTACCAACACACCGC | 55819 |
| rs180952180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030235 | AAAGTAAAAAAAGAT[C/T]ACCTCATAAATACTT | 55819 |
| rs180970031 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073498 | CAGTGAGCAGAGATC[A/G]AGCCACTGCACTCCA | 55819 |
| rs181016684 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179922310 | GGCTTTTAAAAAAAA[A/T]TTCTTTTTTTAATTT | 55819 |
| rs181047162 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179943413 | ATCAGGGAGGGCCTG[A/T]CGTGGACTTTCTACC | 55819 |
| rs181059169 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981472 | ACACACAAAAGAACA[G/T]AGAATGATTTAATAA | 55819 |
| rs181078514 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179950771 | AAGAAAGCACATTAA[G/T]TTAGTAGAAAGAGTA | 55819 |
| rs181085542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927150 | AAAATGGGTCAGAAC[A/T]TAAGTCAGTAATCTA | 55819 |
| rs181088566 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180005913 | AATGAATTATCTTGC[A/C]AACACTATGATCTTA | 55819 |
| rs181137843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975853 | GGTGGCAGGTGCAGC[A/G]CAGAAATGGTTCAGA | 55819 |
| rs181140265 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995192 | ACCAGGCAAACAGTA[C/T]GGGACCTGCCTCTCT | 55819 |
| rs181143380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179955862 | GTTGACTGACTCATC[C/T]ATCTTAGAGGTGCTT | 55819 |
| rs181148631 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179963327 | ATATATGCTCATGAA[A/G]TAAAGTATTTTGCTA | 55819 |
| rs181170300 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180056713 | AAAATGTGTATATAT[A/G]TGTACAAAAGACACA | 55819 |
| rs181171431 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180033532 | AGTTCGAGACCAGCC[C/T]GGCCAACATGGTGAA | 55819 |
| rs181176549 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937559 | GGGGGGATAACAAGT[G/T]TTGGCAAGGAGGTAG | 55819 |
| rs181181269 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988178 | TGTTGGTAGGTTGTA[C/T]GTGGCTAGGAATGTA | 55819 |
| rs181187674 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179970027 | CAGGCATGGCGGTGT[A/G]TGCCTGTAGTCCCAG | 55819 |
| rs181190929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014520 | GTTTGTACATATCAA[G/T]GTAAACCAACAAAAC | 55819 |
| rs181278492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046915 | GAATATGTCTGGCAC[A/G]TAGATGTTTAACATG | 55819 |
| rs181297259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180023795 | TATGTAGATACTCTA[C/T]CCTAAGGGAGATGGA | 55819 |
| rs181477804 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968016 | TACTTAACAAACAGG[A/C]TGGGCGCGGTGGCTC | 55819 |
| rs181486331 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | RNF130 | GRCh38.p7 | 5:179951550 | CACCACGCCCGGCTA[A/G]TTTTTTGTATTTTTA | 55819 |
| rs181502406 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180021034 | GTCGCCAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 55819 |
| rs181503799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051678 | CGTCCATCATTGTTT[C/G]TCTGCTGAACTTAGT | 55819 |
| rs181511749 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073276 | ACCACTGGCCAGGCG[C/T]GGTGGCTCACGCCCG | 55819 |
| rs181511766 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001941 | TATTTCTCTGGGACA[G/T]GGTGTACTATATCAG | 55819 |
| rs181537582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982773 | TATTTTTGTAGAGAC[A/G]AGGTCTCACTATGTT | 55819 |
| rs181539784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028756 | TGGCATATAGCAGGT[A/G]TAAATCGATACCTGT | 55819 |
| rs181557596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023267 | GGAGTTAGGATACAC[A/G]CATGTATTTCCTTGT | 55819 |
| rs181559154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180005299 | CGGGCCTGGTGGTGG[G/T]CACCTGTAATTCCAG | 55819 |
| rs181564029 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179987277 | GGCTCAATCCATCCT[C/T]CTGCCTCAGCCTCCT | 55819 |
| rs181627385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958737 | GGTCACCCAGGCTGG[A/G]GTGCAATGGGGCGAT | 55819 |
| rs181658423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180057626 | CAGGTAGCTTTGGGC[C/T]AGGCGTATGCCAAGA | 55819 |
| rs181663840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936726 | ATTCTAAGACTACTA[C/T]AAAATTACAGTAAAC | 55819 |
| rs181670954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179921450 | AGACCTGTAAATACT[C/T]AGAACTGAAATTACT | 55819 |
| rs181673077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990578 | AGTCTTCTCTAAACT[C/G]CCCCAGGGAAAGGGA | 55819 |
| rs181686176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969763 | GGGAGGCAGAGGCGG[A/G]TGGATCACCTGAGGT | 55819 |
| rs181693783 | snp | A/T | 0.00121581 | 0.0246257 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955215 | ACAGAGAAGAAATTA[A/T]CACAGAGTGAATGTC | 55819 |
| rs181708166 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180061852 | ATCTCTTAGTCCTTT[C/T]GGGCTGCTGTAACAA | 55819 |
| rs181727574 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942710 | AAACTGTAATCATTA[C/G]AGTACATTTGTGAAG | 55819 |
| rs181745949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958277 | ACTAATATTAACAAC[A/C]AGGCACAGGACTGAC | 55819 |
| rs181749587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015859 | ACCAACTAATTTCAA[C/T]GGGAAAGCTGTTTGG | 55819 |
| rs181759835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180010963 | GATTGCATCCATGCC[A/G]ATTTCCAGGTTATGA | 55819 |
| rs181762974 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180046131 | GGTGGACCGCGGCGC[A/G]TGCAGGCCCACAGTG | 55819 |
| rs181774390 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179942926 | TTCTGGCTGGGTGCC[C/G]TGGCTCAGGCCTGTA | 55819 |
| rs181780623 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972655 | TAAAGCCGCAGCACC[A/C]CCTGGGGGGATGGAG | 55819 |
| rs181865659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041470 | TCTGTCAGAGTAAGC[A/G]CCTCAATTTTTCACT | 55819 |
| rs181934494 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179930260 | ATGGGGTTTCACCAC[A/G]TTGGTCAGGCTGATC | 55819 |
| rs181963785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179967375 | GTAAATGTCCATGTT[A/G]AAGAATCCCAGGTAA | 55819 |
| rs181966975 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066042 | AATGTTTAATGTTTT[C/T]ACTGCTGCATAATAT | 55819 |
| rs181987518 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001493 | CCTAAGAGTCTACTT[A/T]GTAGCTGTGATTCTA | 55819 |
| rs182005962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035073 | TCTAATCTTTATTAA[C/T]TCCTTTGTTCTACTG | 55819 |
| rs182040918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058828 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCTG | 55819 |
| rs182041362 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073795 | TCCCCTCCAGCTGGA[C/T]CCTTCATAGGGCAAG | 55819 |
| rs182060948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180037224 | ACTCTCCTACGTGTC[A/G]TCCATGCACATGTGC | 55819 |
| rs182188152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180017413 | TAATTAATAAGCAAT[C/T]TGTGGGCTGATACTT | 55819 |
| rs182188971 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998717 | TGTAAATGTGTTACT[C/T]CCATTTGGTCTAAAG | 55819 |
| rs182192551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938224 | TGGCCTCTCAAAGTA[C/T]TGGGATCACAGGCAC | 55819 |
| rs182198228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979187 | ATCTACACTGTCACC[A/G]TGGTCACCACTCCTC | 55819 |
| rs182204210 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179956534 | AGAGCCCATTACCAG[C/G]TCTTTATAAGAATCA | 55819 |
| rs182209978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945245 | CCTCCACTACGATGA[A/G]CAAGGCTCAGTCCCA | 55819 |
| rs182225802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974674 | AGGTGTGACAGCAGA[C/T]GCTGTGGGGCAGTAC | 55819 |
| rs182230249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179962119 | CTAAGGAATTAGGTG[C/T]GCCATGCTGAAGGAA | 55819 |
| rs182231799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003171 | GCAAAGTCAAGAAAG[A/G]TTTAGCAGGTAAAAC | 55819 |
| rs182236041 | snp | C/T | | | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040475 | AGTCATGGTAACTGG[C/T]TCCTCTTTGGATTTA | 55819 |
| rs182240428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179982458 | TTTTATTTAAGAGAC[C/T]GCCAAAGTGTTTTCC | 55819 |
| rs182251978 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180062420 | CTGCCCTCATGACCT[A/C]ATCACCACCAAAGGC | 55819 |
| rs182255502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179993371 | CCTATTTCTCCACAT[C/T]CTCTCCAGCACCTGT | 55819 |
| rs182257584 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951360 | ACGTCTACAGAACAG[C/T]CCATCCAACAAGAGC | 55819 |
| rs182260272 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180021625 | TTTAAAAATAATAAT[A/T]ATTATTATTATTTAA | 55819 |
| rs182261503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180042531 | AAAATCCTGAAACAG[A/G]TTGTTTACTTTCATC | 55819 |
| rs182273662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020306 | GGAGCAGTGACAGGC[A/G]GGGAAGCACGTGACT | 55819 |
| rs182365080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067692 | TTATGTTAAAATTTG[A/G]TTTTTAGAGCCTCCA | 55819 |
| rs182405032 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928955 | TATTTTGATGAGCAA[A/C]ATTTCTTAATTTTAG | 55819 |
| rs182410850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947772 | TGTGTGTATATGTAA[A/G]TATATAGTAGGTATA | 55819 |
| rs182429149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964536 | GCAAGAAGGCAGAGA[A/G]AACTCTTTACACGTG | 55819 |
| rs182505155 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180061400 | GGGATTCTCTTTGTA[A/T]TAGTTTCCAGTGGCG | 55819 |
| rs182527803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965924 | ATTTCACTGACTCCC[A/G]GACTGGAGAAGGGTC | 55819 |
| rs182536158 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179988847 | TGTTGAGGAAAATGT[A/G]TATTCTGCAGCAATT | 55819 |
| rs182554650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929189 | TTCTTTATAAATATT[C/T]AGTGGAGCCAGCACC | 55819 |
| rs182562747 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:180024632 | GATAAATAAATGTTG[A/G]GAGAATTCATCATCA | 55819 |
| rs182582577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952004 | AAAAAACAAAAAAAC[G/T]AAACCTAAACCAAGT | 55819 |
| rs182617303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983152 | ATGGCAGTTTTTAAT[C/T]TGATGAAGTCGATTA | 55819 |
| rs182631005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013556 | ACTGCAGTGTTAAGA[A/T]CCATATTAACTTGTC | 55819 |
| rs182641520 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179977744 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55819 |
| rs182664207 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180055018 | TGTATTTGAGTTTTT[A/T]AAAAATTACTCTGCT | 55819 |
| rs182790034 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026759 | AAGAAAGCTTAACAA[C/T]CAAACTAAATAACTT | 55819 |
| rs182801718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179930486 | AATCGTTTTCTCTGT[A/G]AAGAGTGACAGTTTC | 55819 |
| rs182809011 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179970604 | TTAAGTTTTCTTTTC[C/T]CCCTTTCAGGACATA | 55819 |
| rs182820222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180048595 | GTGAACTGGGATGGC[A/G]CCACTGCACTCCACC | 55819 |
| rs182822765 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180069169 | TTTCATATAAACCCA[C/T]AGGTTTAGAAACTAC | 55819 |
| rs182828384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180047768 | ATAAAATAAATCTCA[A/G]GCCACTCTTTGTTCT | 55819 |
| rs182841944 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179948680 | ACTCTGTCTCAAAAA[A/G]AGAGAGAGAGAGAAA | 55819 |
| rs182848495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180006651 | ATTTTACATCTGCCC[C/T]GTTCCTAAACAGTAA | 55819 |
| rs182864052 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180044272 | TTATTAATTATAGAG[A/C]CAGGAAAAACTTACT | 55819 |
| rs182866909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054106 | GGTGTGAGCCCCTGC[G/T]CCCGGCCAGCAAATA | 55819 |
| rs182884714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179931630 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCCTGCCT | 55819 |
| rs182897318 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | RNF130 | GRCh38.p7 | 5:179968175 | TGGCGGGTGCCTGTA[C/G]TCCCAGCTACTCGGG | 55819 |
| rs182943596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180031469 | TCCAGCCTGGGTGAC[A/G]GAGTTGAGACTCCAT | 55819 |
| rs183057424 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179989104 | CAATCATAGCAGAAG[G/T]CACCTCTTCACAGGG | 55819 |
| rs183065421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179971475 | CCCGGGTTCACACCA[C/T]TCTCCTGCCTTAGCC | 55819 |
| rs183072139 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179939926 | ACCTCCTTCCTCTGT[A/C]TAATCCTTCTTTGTC | 55819 |
| rs183073733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179957496 | TGCCTTTAATACTCA[C/T]GTTGCAACTGCATTT | 55819 |
| rs183082497 | snp | A/T | 0.00914857 | 0.0670119 | intron-variant | RNF130 | GRCh38.p7 | 5:180025640 | ATTATGAATTTTTTT[A/T]AAAAAAATGTATGAA | 55819 |
| rs183084781 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:180048063 | TGAGCAGCCCTCTTC[A/T]GAGAAATTATTTTTC | 55819 |
| rs183096802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008456 | TATTTTTTCTAAGCA[C/G]CAATGAAACACTGAC | 55819 |
| rs183142316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035726 | CACAGGCATCTGAGG[C/T]TCTGTTCATTTTCCT | 55819 |
| rs183142753 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008952 | ACTTCTCAGTAATGT[A/G]TGGGTAAAAGAAGAA | 55819 |
| rs183258339 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180063993 | GACACAATCACACTG[G/T]GCCCAATTCCATTAC | 55819 |
| rs183266633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932544 | GGATTACAAGTGTGA[A/G]CCACCACGCCCGGCC | 55819 |
| rs183276295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952697 | ATGTAAGAAAATCAA[C/T]GTAATGCACCACATT | 55819 |
| rs183276466 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179991998 | TGATCTGAGAGGAGG[A/T]GCAGCTCAGGAAGTA | 55819 |
| rs183281283 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974063 | TATTGAAGGTGAGTT[C/G]CTCTCACAGCTCTGC | 55819 |
| rs183287946 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179960712 | ACTATTCTAGTAGGT[A/G]TATGCATAGAGGTGG | 55819 |
| rs183343393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923275 | ATATCCAATTGTTCC[A/G]TCGTCGATTGTTTAA | 55819 |
| rs183370091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016867 | GCAAACACATGACAT[C/T]TTATTCTTAAATACT | 55819 |
| rs183389504 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179961875 | TCACACAACTTCAAT[A/G]GCACTGCAGTGGCAT | 55819 |
| rs183415423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057886 | AAGACAGATGTGTGG[A/G]TACCCTTTGTCCCAC | 55819 |
| rs183415607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989517 | ATTTACGTTTTTTAA[C/T]TTTTATTTTTTACAT | 55819 |
| rs183421019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030983 | CTCTTCCTCCTACCC[C/G]CTAAGCCTACTCAAT | 55819 |
| rs183431141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992914 | AGTGTGTGATGTTCC[C/G]CATCCTGTGTCCAAG | 55819 |
| rs183431330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977051 | GGAGGAAGGCTTGGT[C/T]CCATGTGGGGAGCAC | 55819 |
| rs183461600 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947184 | GCAGTTTCTACATTA[A/G]AACAGTTTAAACTAG | 55819 |
| rs183489968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030505 | AAAATTCACTCACGC[C/T]GTTTTTAAAAATACA | 55819 |
| rs183500054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053209 | CAGGGATTGCAACCA[C/T]CTAGAGCTGCAGAAG | 55819 |
| rs183503910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180011926 | ATAAAAATTTTCAAA[A/G]TAAAAAAAATTAAAA | 55819 |
| rs183588147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941712 | CTGCACTGATAGCTC[A/T]TTAATTTCTTAAAAT | 55819 |
| rs183602918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972044 | AAGCTTTTACTTAAG[A/G]GCTGGAAACCCACCA | 55819 |
| rs183613695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974422 | CAAAGGAGAATCAGC[C/T]GTGATCACTGAGCCG | 55819 |
| rs183617585 | snp | G/T | 0.000399281 | 0.0141238 | missense | RNF130 | GRCh38.p7 | 5:179920406 | GAGGGGACAAGGAGT[G/T]TCGATGAAAGAAGTG | 55819 |
| rs183629786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019674 | CATTCTACATTCTTT[C/T]AGGAAATGAATATAG | 55819 |
| rs183631525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039689 | TACACGATGAAAAGT[C/T]AGTTCTTTAAATAAG | 55819 |
| rs183649256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001367 | ATGACAATGGGACCA[C/T]GTCCTAGGCTCAGAG | 55819 |
| rs183649862 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944886 | TAGCATGACAGCAGG[A/C]CCTGTTTCCAGATAA | 55819 |
| rs183659480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925317 | TGCCCACGTAATGAA[A/G]CCTCCATAAAAACCC | 55819 |
| rs183671697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013404 | AGGTAACTACTATAA[C/T]GTCTGGTAATGGAAA | 55819 |
| rs183673049 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060863 | TCACGAGGTCGGGCG[A/T]TCGAGACCATCCTGG | 55819 |
| rs183692807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964132 | GTAAAAAGGACATCT[C/T]ACTGGTGTCTCAAGA | 55819 |
| rs183723083 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997061 | TATATGTGTCTGGGA[A/C]AATTTACTAGTGGTT | 55819 |
| rs183752409 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179944328 | CAATAAATTAAATAA[C/G]TAAAGGATCTGACAA | 55819 |
| rs183766419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180068657 | GCCAAACTGATAGTA[A/G]CACTGCAAAGCGAAC | 55819 |
| rs183870422 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180044745 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 55819 |
| rs183873081 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022894 | GGTGGGAAAAGAAAC[A/C]TTAAGTAGAGAGTTC | 55819 |
| rs183942257 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922514 | GATGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 55819 |
| rs183999155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003729 | TCTATTTGCATCCGG[C/T]TAACTCTCAAGTACC | 55819 |
| rs184018777 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF130 | GRCh38.p7 | 5:179968534 | AGCCAGGTGTGGTGG[C/T]AGGTGCCTGTAATCC | 55819 |
| rs184033003 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043261 | GCCCAGGAGTTCAAG[A/T]TTACAGTGAACTATG | 55819 |
| rs184091457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065285 | TGTCACCCATTATCT[A/G]ATCGATATAACACAA | 55819 |
| rs184119408 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180027330 | GAGGAAGGGAACTGA[A/G]TAACACATTGATGAG | 55819 |
| rs184121178 | snp | C/G | 1.66385e-05 | 0.00288426 | intron-variant | RNF130 | GRCh38.p7 | 5:179967053 | ATTGTAAGGAAAACA[C/G]AACCTTTCATAAGAT | 55819 |
| rs184128995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990082 | ACGAGAGATTGCAGA[A/G]ATAAAGACACAAGAC | 55819 |
| rs184131791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180070501 | AGTGTACAAGCAAAT[A/C]ATGACTTTATTTAGG | 55819 |
| rs184162404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984288 | TTCCTTTTTACTTAC[C/T]GTGCTGGCTAGAATC | 55819 |
| rs184180543 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180063575 | CATGAACCTAGAGAG[A/G]CCTAGGCTAAAAATC | 55819 |
| rs184186300 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180021737 | CATGATGCCTCATCA[A/C]CCCCGAATATGTGGT | 55819 |
| rs184252473 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981490 | AATGATTTAATAAAG[A/C/G]CTTCCCTATGTATCT | 55819 |
| rs184256430 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009415 | CAGTGAAAAACAATC[C/T]AGGTAGAAAATGGGC | 55819 |
| rs184290781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981017 | GAGGCAGGGGAGGAA[C/T]GTCAGGGAAGGTCTT | 55819 |
| rs184291491 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180049695 | AGGTTAAATCAGACT[C/G]CAAAAGGAGTCTCAA | 55819 |
| rs184295580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929966 | TGTATAAAAGCCTTG[C/T]GTATCTTCTCTTACA | 55819 |
| rs184305668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950442 | CATTTTGATACTAAT[C/T]GTATTTCTGGTTTTA | 55819 |
| rs184319777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180019107 | AATCACTTTGAGGCC[A/G]GGCGGGGTGGCTCAC | 55819 |
| rs184323755 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180000746 | TGATTCTTACTTCTC[G/T]TTTATTCAATTTCCT | 55819 |
| rs184362039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022061 | TTCAGGTCAGGTGCC[A/G]CTGGCAGTAACAACA | 55819 |
| rs184364526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003927 | TAACTAAGGTTTATT[C/T]GGTACATACCATGTG | 55819 |
| rs184385032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958363 | CACATGGGAGTACTG[C/G]GTCACAACACAAAAT | 55819 |
| rs184401372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179985419 | TGTGCATACTAAGCC[A/G]TAAGGGTCCTTAGGA | 55819 |
| rs184402984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180010226 | CACTCCAGCCTCGGC[A/G]ACAGTGAGACTACAT | 55819 |
| rs184415687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954400 | GAGTGTTAACCACAC[A/G]AAGAAGTTCTGACAC | 55819 |
| rs184416447 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179990534 | GGGCCTGACATCAGT[C/T]GGGCCTTCCACAAGA | 55819 |
| rs184421310 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179972283 | ATCTGATAGAAGTTA[C/G]AGAACCTCCCTCTGA | 55819 |
| rs184491743 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926606 | TGAGCCGAGATAGCG[A/C/T]CATTGCACTCCAGCC | 55819 |
| rs184498973 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179935141 | TATATTGTTTAATTC[C/T]AAACATTTGGGGATC | 55819 |
| rs184512929 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179984529 | TTTTAGCTTTTTTGG[C/T]CTGCTAATATGGTAA | 55819 |
| rs184523052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968634 | TCACACCACTGCACT[C/G]CAGCCTGGGTGACAA | 55819 |
| rs184527951 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933424 | TGTGTGTGTGTGTGA[A/G]TGTGTGGTAAAAAGC | 55819 |
| rs184533830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953614 | TACCTTACACCGTAT[A/G]CAAACATTAACTCAA | 55819 |
| rs184536563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969096 | CTGTTGGATCAAACT[A/G]AACTTTTTGTTCCAT | 55819 |
| rs184544666 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179929515 | CACTTTAGGAGGCCA[A/C]GGTGGGAGGACTGCT | 55819 |
| rs184570728 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180004286 | TCACTGATATTCTCC[A/G]TACTTCACACTGTGC | 55819 |
| rs184621618 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072775 | ACTCACCTCCTGCTC[G/T]CTTACTGGTTCCTCG | 55819 |
| rs184623304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940573 | GTTACTTTTATGTTA[C/T]GAGAATTTCATCTCA | 55819 |
| rs184625180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028189 | CGACTCGGATGCTGT[A/T]TCCTCAAGGCATTCC | 55819 |
| rs184630335 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180051517 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 55819 |
| rs184654805 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180056799 | ACAGGCCCATGGACA[A/G]CAGAATGCATAACTA | 55819 |
| rs184750984 | snp | C/T | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919846 | AGGAAGTAGAATAAG[C/T]GAGAGGGGAACATCC | 55819 |
| rs184790709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179935922 | CCCTCCCATCTTTTG[C/T]GCAGTTGATGTCAAG | 55819 |
| rs184813262 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969683 | ACCCGCCTGAACATC[C/T]TGTCTCTTCAAAACA | 55819 |
| rs184815394 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180014050 | TTCCAGAGACAGGTC[C/G]AGGCTTCAACATTCT | 55819 |
| rs184818692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994008 | CATTTCTTGTTTTTG[A/T]CAGCTTTGTCAAAGA | 55819 |
| rs184821824 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954724 | TGTGAATTACATTTT[G/T]ATTGCAAAAATCCTT | 55819 |
| rs184826382 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179974939 | ATTGCTTCCTCTGGG[A/C]AGTCAATGGTGAAGC | 55819 |
| rs184845608 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031984 | TTTGGTTGCACTGTT[C/G]TTTTGATTGCATTTG | 55819 |
| rs184885014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971730 | TATACCTTTACAACT[C/T]TGATTGTCAATTTCT | 55819 |
| rs184925915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038841 | AGAAAGAAAAATACA[C/T]TTTGCTCAGTTGAAT | 55819 |
| rs184966976 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062822 | GACTTGTTGACTACT[A/G]ATGGCCATTACATTC | 55819 |
| rs184982319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994761 | CCCAAGTGCTGTGCA[C/T]TTATGTAAGCAGATG | 55819 |
| rs184995510 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962925 | TGGTCGCCATTTTGC[C/T]CATGGAGATAGCGCT | 55819 |
| rs184999253 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RNF130 | GRCh38.p7 | 5:179957904 | TTTTTTTGAGACGGA[A/G]TCTCGCTCTGTCGCC | 55819 |
| rs185018865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032268 | GAACTTCTTGTTCAA[A/C]ATCACAGACTATCTT | 55819 |
| rs185075578 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060020 | GTGTCTTTTAAATGT[C/G]GGTGACAGACGGAGA | 55819 |
| rs185100995 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | RNF130 | GRCh38.p7 | 5:179975274 | GTGGCATCTGCTGGG[A/G]TGAGGCTTGAAGAGC | 55819 |
| rs185117590 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056537 | TGGCAAAACACACTG[A/G]GCAGAGGTGGTGTTA | 55819 |
| rs185128027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180014130 | GTCTGCCCACAAGCA[C/T]AGGCTATGCAAGTTA | 55819 |
| rs185139613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179991153 | TAGTGTATCTTTCCC[C/T]ATCTGCTGAGAAAGT | 55819 |
| rs185152143 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179922408 | ACCTCCACCTCCTGG[A/G]TTCAAGAGATTCTTG | 55819 |
| rs185153617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179973635 | CCGCACGCCTGACCG[C/T]GCTCACCCTCACTAT | 55819 |
| rs185157405 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179944057 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 55819 |
| rs185161397 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960005 | TAGTCACGCCTCCCA[C/G]TAAACTTCAAATCTC | 55819 |
| rs185190005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949829 | AGACCAGAGATGAGA[C/T]CCCTCAGATCACCAC | 55819 |
| rs185246409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921019 | ATAATTATATTTTGA[C/T]TTTAAAATTCCATAG | 55819 |
| rs185251861 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179946610 | CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTTGGC | 55819 |
| rs185254653 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180059730 | TGCTAAGCCTTAGAA[A/G]AATTTCACAAATGAT | 55819 |
| rs185267241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018212 | AGGCAGAAGAATTGC[C/T]TGAACAAGGGTGGTG | 55819 |
| rs185334682 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999662 | GCGAAGGTTGCAGTG[A/G]GCCAAGATTGCACCA | 55819 |
| rs185357630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966308 | TTAAGTGCCAAGAGA[C/T]CAAACTTCCATAAAA | 55819 |
| rs185365719 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038423 | TTTGTTTTTTTTTTT[A/C]TTTTGATTAACCTAG | 55819 |
| rs185369769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942849 | CAGTTATGTGTAACT[C/T]TCTCCTGTGGATATA | 55819 |
| rs185393324 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179995912 | ATTTTGCTTTTTCCA[A/C]GTGGGTTAGGCATGC | 55819 |
| rs185396192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047059 | ATGTTCTATCAGTTG[C/T]TTCCTACAAAAGAGG | 55819 |
| rs185397757 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179976058 | CCAGACGTCAGGCTC[A/G]TGCCTGTGATCCCAG | 55819 |
| rs185400128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067197 | GTCATCTGACAGGTA[A/G]CTAAGCCTTAGCTCC | 55819 |
| rs185401085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927298 | CACCTGGAAATACAC[A/C]AGATGTGTACTGGTC | 55819 |
| rs185405264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963416 | ATGAAAACTGCTCCA[C/T]GTGTTTTCCTGGGAT | 55819 |
| rs185407477 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179946709 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 55819 |
| rs185471131 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061997 | CTTCATCAATGGAGA[A/C]TTCTTTGTGTCCTCA | 55819 |
| rs185486829 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073362 | GACCAGCTTGGCCAA[C/T]ATGGTGAAACCCCGT | 55819 |
| rs185492941 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180042024 | CTCCAGCCTGGGTGA[C/T]AGAACAAGACCTTGT | 55819 |
| rs185619744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014587 | TCCTTCTTCAATGAA[C/T]AACACATTGAAATAT | 55819 |
| rs185621418 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | RNF130 | GRCh38.p7 | 5:179968156 | AAACATTAGCCGGGC[A/G]TGGTGGCGGGTGCCT | 55819 |
| rs185631412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951573 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 55819 |
| rs185649892 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180021407 | CAACCACAAGGTACA[A/T]CATTATGTATCATGA | 55819 |
| rs185650069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179930866 | AAACATAACAAAACC[C/T]GGTCTCTACTAAAAT | 55819 |
| rs185650258 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180002604 | CTGGTGGTGAGGTCT[A/G]TAGGTATCCACAGTG | 55819 |
| rs185666703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983113 | CCAGATAAAAATCCT[C/T]TTGCATGTATTTCCC | 55819 |
| rs185671012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969867 | GTGGTGACGGGCACC[C/T]GCAATCCCAGCTACT | 55819 |
| rs185677827 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955361 | TCAATCCCTGTTCCT[C/T]TCACGGGAGCCAGGA | 55819 |
| rs185690739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946482 | AGAGTAAAGAAAGTG[C/G]ATAATTTCTACAAAT | 55819 |
| rs185706688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005406 | TGTACTCCAGCCTGG[A/G]CGACAGAACAAGCCT | 55819 |
| rs185706923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987857 | TTTGATGTGTTGTTG[A/G]ATTCACTTTGCTTCG | 55819 |
| rs185718322 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179928728 | CCGCCTCCTGGGTTC[A/T]TGCCATTCTCCTGCC | 55819 |
| rs185720083 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066237 | GTGATAGTGAATAAG[A/T]CTCACCAGATCTGAT | 55819 |
| rs185720605 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180004990 | ACACCATCTGCCTGT[G/T]CCCAGATCACTCCTC | 55819 |
| rs185738191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023271 | TTAGGATACACGCAT[A/G]TATTTCCTTGTTCTG | 55819 |
| rs185738426 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180046574 | AGCCTCGGACAGTAT[G/T]TTTCTGCAGTGATGG | 55819 |
| rs185741048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045009 | GAACCCCTGAAACTT[C/G]CGCAGCCAGGAAGGA | 55819 |
| rs185788722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962393 | TCTATAGCCAGACAA[C/T]GGGCAGTCAATTACA | 55819 |
| rs185809913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030264 | TTGCTTTGTCTCTCC[A/G]AGTAAGAATACTTGA | 55819 |
| rs185816244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179925966 | GGATGCATGTGGCAC[A/G]GAAAGGGGGAGCAGC | 55819 |
| rs185838103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023112 | TAGGAGTGGGAGTTT[A/G]GTGATAAGAAAGGAG | 55819 |
| rs185843925 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073598 | TGACTTGGCAGACAT[C/T]CTTTACAATTTCTCC | 55819 |
| rs185860998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986348 | CAAGCAATACAACTT[C/T]TTCTTGTAACGTCAT | 55819 |
| rs185865329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065846 | TTCTCTCTTTTTTTA[A/G]TTAAACTTTCATTAC | 55819 |
| rs185905745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951049 | AGGCCAAACATGCTC[A/G]GCTGAACTCTGGCAT | 55819 |
| rs185946295 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180052479 | TTGATCCAGAGCAGC[C/G]CCTGAAGGCACTACT | 55819 |
| rs185954517 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RNF130 | GRCh38.p7 | 5:179951414 | TTTGAGATGGAGTCT[C/T]GCTTTGTCGCCCAGG | 55819 |
| rs185957294 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011322 | GTCTATCAATCAGAT[A/T]ATGTATTATATCAAT | 55819 |
| rs185960936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930302 | ACCTCGTGATCTGCC[C/T]GCCTTGGCCTCCCAG | 55819 |
| rs186033890 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956156 | CATCAGGTGTAAAAA[C/T]AGCCTATGACCTTTT | 55819 |
| rs186145854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937808 | CCCAAATGTCCATCA[G/T]TGGATGAGGAGATGA | 55819 |
| rs186262120 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179988289 | CAGTTGTAATGTCTC[C/G]TTTTTCACTTCTGAT | 55819 |
| rs186306392 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180024071 | CTAATTATAAGAAAA[C/T]TATCAAACATGTCCC | 55819 |
| rs186363395 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179974297 | CCACGCGGCAACTCC[A/C]CTTCTGAAAACGTAC | 55819 |
| rs186379428 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180030542 | CTTTTTGGTGTTTTA[C/T]TTTTGTTTTTTAAAA | 55819 |
| rs186390966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012772 | ACTGGTTTAAAAATG[C/T]AACTTTGTGCTATTT | 55819 |
| rs186396127 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179992028 | AATGCTAGCAATGGG[A/G]AGCGACTGTAAATAC | 55819 |
| rs186413824 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180053997 | AATTTTTATATTTTT[A/G]GCAGAGATGGGGTTT | 55819 |
| rs186419401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005990 | ATGTAATATTTAGAA[A/G]GTATATAATACAGTC | 55819 |
| rs186430167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970087 | TTGAACCCAGGAGTT[C/T]GAGGTTACAGTAAGC | 55819 |
| rs186448442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057470 | AGGAAATTGCCGGAA[C/G]CTAGGAGGTGGAGGC | 55819 |
| rs186480948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942984 | GGTGGATCATGAGGT[C/T]AAGAGATCGAGACCA | 55819 |
| rs186507808 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180011097 | ACATTTTCACAAAAC[A/G]CATATAACCTGAAAC | 55819 |
| rs186514340 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972730 | CTTTTCTTATTGTTC[C/T]GTCTTTCTTTTCTCT | 55819 |
| rs186518944 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180051698 | CTGAACTTAGTTACT[A/G]TGTATCTCAAATGGA | 55819 |
| rs186531441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962191 | GCTGGATGAGGTGCA[A/G]TGCTCCTCTGAAGGC | 55819 |
| rs186554343 | snp | A/G | 0.0260434 | 0.11132 | intron-variant | RNF130 | GRCh38.p7 | 5:179925391 | GAGGTACCGGTAGGG[A/G]AGGGCACTGAACTCC | 55819 |
| rs186559154 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945351 | GCAAAACCTCAGCGG[C/T]GGGGGCTTTTCTGGG | 55819 |
| rs186560747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013627 | AATGTGACAACAGAC[A/C]GCAACATAACATTAT | 55819 |
| rs186567127 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993443 | AGATGGTATCTCATT[A/C/G]TGGTTTTGATTTGCA | 55819 |
| rs186567492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042685 | TTAGGTGTTCTGTTC[A/G]TTATTTTTCAAAACA | 55819 |
| rs186569603 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180021628 | AAAAATAATAATAAT[A/T]ATTATTATTTAAAGA | 55819 |
| rs186569731 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974734 | TTAAAAACTGGACTG[A/G]GAAATGCGAGTGTCA | 55819 |
| rs186576196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964316 | AGACTGTCTCTCTCT[C/T]TCCATCCAGATATTC | 55819 |
| rs186587829 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180034637 | CAGAAAAAAGTAAAC[A/T]TAGCAGGTTTGAACT | 55819 |
| rs186593677 | snp | C/G | 0.000820702 | 0.0202405 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015421 | AGAAATCAGTTGAGG[C/G]TCCCTCTTGAAGACT | 55819 |
| rs186594055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996663 | CCCTGGGATAAATCC[C/T]ACTTTTTCATCATGA | 55819 |
| rs186602960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997151 | TTTTTTAAAATTTTA[C/T]TTCTTTTGGAGACAG | 55819 |
| rs186664951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921500 | AGAAACTGCCAGGCT[G/T]TTCTAAGATGGTCCT | 55819 |
| rs186699629 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179958755 | GCAATGGGGCGATCT[C/T]GGCTCACTGCAACCT | 55819 |
| rs186726122 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179990666 | CGCTAGACCATGGTC[C/T]GCTTGGTAATGGGCG | 55819 |
| rs186755768 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180031587 | CTCACTGTTCAAGGG[C/T]CAACTGTAATTGCTA | 55819 |
| rs186763647 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180029531 | ATGAGTAGTTTGCAG[A/G]TAATTCACAAATTCC | 55819 |
| rs186793306 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977296 | CATAATCCAGGTTTA[G/T]AAAAAGATTTAATCC | 55819 |
| rs186835850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016199 | TTTACAGAATCTGGC[A/G]AAAGTTATATAGGAG | 55819 |
| rs186865645 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180057689 | AGCTCCTGGTCATGG[G/T]ACCCTTCCAGACCTT | 55819 |
| rs186919266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964634 | CCTAACCCTGCATGC[A/G]GAATTGTGTGTGCAT | 55819 |
| rs186938563 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179929053 | GCCTATCTGAAGGTT[G/T]TGATGACATTTTATC | 55819 |
| rs186941182 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016929 | ACGTGGCCACAATTC[A/G]TTTACTTATCCTCAA | 55819 |
| rs186948257 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179948211 | CTCTCATTCAGATAT[C/T]GCGAAGATTAAAATG | 55819 |
| rs186953935 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919892 | AGCAGCACCTGTACT[C/T]CACGCGGGTAGGAAG | 55819 |
| rs186954117 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179997532 | ACGGGGTTTCACCGT[C/G]TTAGCCAGGATGGTC | 55819 |
| rs186956264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977849 | GACAGAGCGAGACTC[C/G]GTCTCAAAAAATAAA | 55819 |
| rs186974389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035764 | ATTCTTCCCTCTACT[A/G]TTTTGAATCTGCTGT | 55819 |
| rs187047694 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179967671 | ATTTGTTTACCTAAC[A/C]ACCTTTGGTTCTCTC | 55819 |
| rs187108738 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RNF130 | GRCh38.p7 | 5:180020569 | TCCTGAGGACAGTGG[G/T]CTACAGCTTGTCACC | 55819 |
| rs187112887 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960741 | GGAGTTTAGTATCAA[G/T]TTTTGGACAGTCATT | 55819 |
| rs187120221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179982627 | GCTTCCCAAACTGGA[A/G]TACAGTGGTGCAAAC | 55819 |
| rs187135593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070081 | GCTTGCCTCCCCTTC[C/T]TCTTTCTACCCTTCC | 55819 |
| rs187141223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061558 | AGCCCCTCTCCCAGC[A/G]TCTGATGGCTGCTAG | 55819 |
| rs187179989 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984665 | TTTAGAATTTGTGCA[A/T]CTATGTTCAAGAGGG | 55819 |
| rs187187514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968790 | GGGACATCTGGCAAC[A/G]TCTGGAGACATTTCT | 55819 |
| rs187190386 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179924817 | ATAAATAAAAAATTT[A/T]AAATGGGATCAATTC | 55819 |
| rs187191111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180047864 | TTTCCTCCTGCACTA[C/T]CACAGTCATTCTTTG | 55819 |
| rs187192958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953822 | AGAAAGTGAATAAAT[A/G]GTTTAGAGAATGTGA | 55819 |
| rs187198690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007298 | CCCAGCTACGTGTGA[A/G]GCTGAGGCAGGAGAA | 55819 |
| rs187199962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022154 | TGCCATTACTAGTAA[A/C]GTTCACTTTGATAAT | 55819 |
| rs187202891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180044457 | GCTCCTCACCTCAAT[A/G]AATAGTAACTTATGT | 55819 |
| rs187223208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004122 | GCTGAATTAAGGGGA[A/G]GAACGATCTTGGAAA | 55819 |
| rs187235330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063999 | ATCACACTGTGCCCA[A/G]TTCCATTACCGCTGA | 55819 |
| rs187284935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001792 | GGGGAGGATAGCACA[C/G]TGATAATTCCACTCT | 55819 |
| rs187331782 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180040880 | AAACAATGAAAATTT[A/C]TTAACTTTACAGACT | 55819 |
| rs187376436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977001 | CCAACATGCTGTTTC[C/T]AGGGCAACCAGGCAC | 55819 |
| rs187395842 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179946977 | CAACTCCTTGGCAAA[G/T]AAAGTACTCTCCTTA | 55819 |
| rs187396629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989396 | TATCTATCCCTTGAG[A/G]CCTAGTAATATTAGC | 55819 |
| rs187401825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179971586 | ATGTTAGCCAGGATG[A/G]TTTCCATCTCCTGAC | 55819 |
| rs187410124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180025260 | TTAAGAACATCCTCC[A/G]TCCTGGAACCTAGGA | 55819 |
| rs187414909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048362 | CCTGCTTCTAGGCTA[A/G]AGGATGATATTATTA | 55819 |
| rs187416998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025906 | GTGGCCCAAATTACT[A/G]ATACGTAAAGGTATT | 55819 |
| rs187421626 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180008576 | TCAAACCAGAAATCA[C/G]TAACACTAAGATAAT | 55819 |
| rs187433017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068232 | GCACATTTACAATGT[C/G]TGCTCCACAGCAGAC | 55819 |
| rs187440495 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931809 | ACTACAGTACAAAGA[C/T]TTTGTAACTGTGATT | 55819 |
| rs187475954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003188 | TTAGCAGGTAAAACC[A/G]ACAGAACCTCATGAC | 55819 |
| rs187499194 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968453 | GGCAGATCACTTGAG[A/G]TCAGGAGTTTGAGAC | 55819 |
| rs187590506 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927930 | ATAAATGGAAACAGG[G/T]AATATATTCTTTTGT | 55819 |
| rs187618574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068747 | CTCTAGGAAAACTAT[A/G]AAGTTCTTTTGTCTT | 55819 |
| rs187648106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963875 | TAAAATTGCACAAGG[A/G]CATAGATTTTTTTCA | 55819 |
| rs187708341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952561 | AGAATTAATTACATA[C/T]CAATATCCCTTATAA | 55819 |
| rs187739389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180056070 | GCCTGGGCGACAGAG[C/T]GAAACTGGGTCTTAA | 55819 |
| rs187740887 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179983554 | GGCTTTGTAATAGAT[A/C]TGAAATTAGGTGGTG | 55819 |
| rs187756714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032108 | TTCTGGATGCAAGTC[C/T]TATATCAGATGTATG | 55819 |
| rs187783249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059156 | CCACAAGTACATCAC[A/G]GTTTTTGCACCTTTT | 55819 |
| rs187797275 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179953083 | AGATGACATGATCTT[A/G]TAGACAGAAAAGCCC | 55819 |
| rs187800992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018009 | ATTGAGAAAGAAGAG[C/G]TTCAGGCTGGGCGTG | 55819 |
| rs187802851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037871 | ATAAAGCCGTTTCCT[A/G]TTGCTCTTATGCACA | 55819 |
| rs187835892 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179932555 | GTGAGCCACCACGCC[C/T]GGCCTTAGCTAATAT | 55819 |
| rs187836265 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179968559 | TAATCCCAGCTACAA[A/G]GGAGGCTGAGGCATG | 55819 |
| rs187934689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180058014 | ATTGAATTAAACTGT[A/G]GGACATCCAATTGAT | 55819 |
| rs187941681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026777 | AACTAAATAACTTAA[C/T]AAAATCATTTCAGAG | 55819 |
| rs187948222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179989868 | TCCTTTCTCTTCTTC[A/G]TGTAATTGTTTTATG | 55819 |
| rs187987241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180013481 | TATGCTGGCACCAAG[C/T]AGGAACATGTAATTT | 55819 |
| rs187988524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055362 | CCACCATGCCCAGCT[A/G]GAAGTAAGTTAAGTT | 55819 |
| rs188028649 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180054751 | GGTATTTTCACAGGA[C/T]GGTCTGAATGTGTAG | 55819 |
| rs188075185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988852 | AGGAAAATGTGTATT[C/T]TGCAGCAATTTGATA | 55819 |
| rs188080813 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179938534 | TGTCACTAAATTGTT[C/T]ACTTACTTATTCATT | 55819 |
| rs188082696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970718 | ACACCGTGTAAGAAC[C/T]GCTAAGTAGGATTTG | 55819 |
| rs188089071 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179957239 | CCACATGGCAAAACC[C/T]CATCTCTACTAAAAA | 55819 |
| rs188133035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944974 | TTAATGGTATCTGCA[C/T]CTGTTGAAAGTTATA | 55819 |
| rs188153312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179927534 | ACTATGTCCTCTCTC[C/T]CCCGCCAAAGGAAAC | 55819 |
| rs188154686 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179974517 | AAAAGGAAACGTCAC[A/G]TGGCAAGAAGCAGGC | 55819 |
| rs188161239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946854 | CCACCGCGCCCAGCA[C/T]CATAGGGGATCTTTT | 55819 |
| rs188165613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940622 | ATTGAGATAAAGTAT[C/G]TTTTTCTCTGCCTTT | 55819 |
| rs188192468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971967 | TTATCAATCTAGTCT[C/T]AAATTCACAGACAAT | 55819 |
| rs188195877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179939941 | CTAATCCTTCTTTGT[C/T]ATAAACGTCCCTTTT | 55819 |
| rs188231288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008966 | TATGGGTAAAAGAAG[A/T]AGTCTCAAAAGAAAA | 55819 |
| rs188253994 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180049275 | ATGAGCTATTTGGGA[C/G]TGGAGAGCCCCACTT | 55819 |
| rs188272479 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031218 | AGGGCTGGGCACGGT[A/G]GCTCACGCCTGTACT | 55819 |
| rs188286213 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179993187 | ACGCAATAAACATAC[A/G]TGTGCATGTGTCTTT | 55819 |
| rs188386925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996365 | ATAACATGTTAAATA[C/G]AAGTGGTGAAAGTGG | 55819 |
| rs188399300 | snp | C/T | 0.000108342 | 0.00735931 | intron-variant, missense | RNF130 | GRCh38.p7 | 5:179963478 | TTACTTACTCATTAG[C/T]ATTCAAGCTAGCTGT | 55819 |
| rs188409289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034443 | GAAGGATTAGTATTA[C/T]TTTTTCTTTAAATAT | 55819 |
| rs188421169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015011 | AAATACAACAGTAAA[A/G]GGAGTTTTATGGAAA | 55819 |
| rs188425358 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180065478 | TAAAGTACAGGCACT[A/C]GGCCGGTCACGGTGG | 55819 |
| rs188434929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179934637 | TCACTGCGAACTTAT[A/G]GGTTCAAGTGATCCT | 55819 |
| rs188438080 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922762 | AACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT | 55819 |
| rs188447119 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057100 | GTCTGTGCTAATAAG[A/C/G]TGACTCTTGGAAGAT | 55819 |
| rs188451736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961977 | TCATAACAACCCTGC[C/G]ATATGGTCCTAGCAT | 55819 |
| rs188481455 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180038776 | TTTATTAAAAGACTC[G/T]CATTCTAGCTACTTC | 55819 |
| rs188498642 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180060172 | CTTGCCAACACCTTG[C/G]TCTCACTGAGGCCAG | 55819 |
| rs188532638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957548 | CTTCAACCACATTAT[C/T]TGGCACTATCCTCCT | 55819 |
| rs188548753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980269 | TACTTTATTTTTAAG[C/G]AATTAAAAGTATAAA | 55819 |
| rs188629945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066315 | GCTGCCGCCATGTAA[A/G]AAGTACCTTCTGCCA | 55819 |
| rs188637675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046583 | CAGTATTTTTCTGCA[C/G]TGATGGTCAAAACAG | 55819 |
| rs188638150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179981107 | GGAGGGGGTTCCGGG[C/T]GTAGGGGTAGGAGTG | 55819 |
| rs188639770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023544 | TAAACTAAACCAAAA[C/T]AAAAAAACAAAAATC | 55819 |
| rs188653002 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179950722 | AGCATCTATTTTTTT[C/G]AAGTCTTAATACTAT | 55819 |
| rs188663216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039242 | CACCTTACTTCTTTT[A/C]TTTTCTTTTTTTTTT | 55819 |
| rs188667686 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180019152 | CACTTTGGGAGGCTG[A/G]GGCAGGTGGATCACC | 55819 |
| rs188671942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000747 | GATTCTTACTTCTCT[C/T]TTATTCAATTTCCTG | 55819 |
| rs188707661 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984467 | AAATCAGGAATCGAT[C/G]TTGGACTTCGGCAAA | 55819 |
| rs188712849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926826 | ACAGTCTTGTGGGAC[C/T]GAGCCCTCACCCTGG | 55819 |
| rs188719257 | snp | C/T | 0.030278 | 0.119257 | intron-variant | RNF130 | GRCh38.p7 | 5:179946639 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 55819 |
| rs188733685 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179944520 | CCAGGCTGGAGTGCA[G/T]TGCCACAATCTTGGC | 55819 |
| rs188738677 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021766 | GTATTTTCCTACAAA[C/T]AAAATTTATAAACAT | 55819 |
| rs188764698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063585 | GAGAGGCCTAGGCTA[A/C]AAATCAAGATACGGG | 55819 |
| rs188766913 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180059861 | AAAGACGTCCATCTC[C/T]CAATCCCCAGGACCT | 55819 |
| rs188784057 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018752 | GCCCAGGGATCTGCT[A/G]ACCAACACAGTCCTG | 55819 |
| rs188792280 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179979471 | TAGAATTGGGTGTGG[C/G]GCAGGAGACAGTTTT | 55819 |
| rs188941297 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179949287 | TTTTTTTTTTTAAGA[A/C]AAGGTCTTGCTGTGA | 55819 |
| rs188958970 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929877 | ACACCTCCATAGTAT[C/G]GTGTCACTCATTTCA | 55819 |
| rs188969485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949979 | CTCCAGAGTGGAACA[C/T]TGACCCCATTTGTTT | 55819 |
| rs188969656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966435 | CGGAGGTGGAGAGCA[C/T]GAGCGCTCACAGCAT | 55819 |
| rs188983667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180003793 | ACTTTTTATTAAAGT[C/T]TCTTACCTTCACCTA | 55819 |
| rs189007336 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044202 | AATAACGGTACTTCC[A/G]TTTTTCTTACCTGCC | 55819 |
| rs189037767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180010846 | GTGAATCTACACATG[C/T]GATAAAACTACACAG | 55819 |
| rs189050406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990564 | AGGTGGTGGAGCAGA[A/G]TCTTCTCTAAACTCC | 55819 |
| rs189054717 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179969636 | ACTTTGGGAGGCTGA[A/G]GCAGGAGGATCACTT | 55819 |
| rs189064647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051559 | CAGAATTTTTAAGAA[A/G]GTGGCAGCAAAATAC | 55819 |
| rs189065947 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179998930 | GTGTATATATATTTA[C/T]AATGATTATATCCTC | 55819 |
| rs189066410 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073091 | TTTGGCGTCTTCTGA[A/C]CAGCCAGGGTTGAGT | 55819 |
| rs189072729 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180028468 | TTCGTCTACTGAGAG[A/G]ATTTTCTCTTTCTGG | 55819 |
| rs189072977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935293 | CAGCATATAAGTCTA[A/T]CTTAGTAAATAATCT | 55819 |
| rs189214215 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179929281 | TGTCTGTACATGCAC[A/G]GCTGTTTCAGAACTC | 55819 |
| rs189233862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965960 | AGCCTCAGGGCGTGA[C/T]GTGCTAGGCAAGCAG | 55819 |
| rs189279373 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179969760 | TTTGGGAGGCAGAGG[C/T]GGGTGGATCACCTGA | 55819 |
| rs189281040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014105 | TCCAGCCTCTAACAG[C/T]TGTCCAGAGGTCTGC | 55819 |
| rs189283102 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179994182 | CCAGTTTTGTTCTTT[C/T]GGCTTATGCGGGCTC | 55819 |
| rs189286166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004522 | AAATGCTGAAAAGAC[C/T]TTCTATAGCATACAG | 55819 |
| rs189287288 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954762 | CCTGCTGATTTGAGC[A/G]TGACTACTGGAGTGA | 55819 |
| rs189303028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179936147 | CTTATCTTGAGACAG[G/T]GTCTCGCTCTGTCAC | 55819 |
| rs189309561 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180005249 | CCTGGCCAACATGGC[A/G]AAACCCCGTCTCTAC | 55819 |
| rs189314427 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RNF130 | GRCh38.p7 | 5:180044819 | CCTGGGCGACGGAAG[C/T]AGACTCCGTCTCAAA | 55819 |
| rs189321633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986539 | GGGACGAACTACTCA[C/T]AAGCGTATGTCACAT | 55819 |
| rs189327496 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179972082 | GGTAAGCCCCAGATA[C/T]ATTCAGTACACCTAA | 55819 |
| rs189333794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958087 | TTTCACTGTTTTAGC[C/T]GGGATGGTCTCGATC | 55819 |
| rs189348633 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179954486 | AAAGGCCACATATTA[G/T]ATGGTTCTATTTACA | 55819 |
| rs189355084 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179941759 | ACTTTTTCCATATTT[A/C]TAGTTCTTCTTGATA | 55819 |
| rs189357533 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010043 | ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT | 55819 |
| rs189361501 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179990205 | TATTTATTGGATACA[A/G]AGTAAAAGGGGCAGG | 55819 |
| rs189394011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030008 | GTGTACCACCACGCC[C/T]GGCTAATTTTTGTAT | 55819 |
| rs189520591 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040149 | CATAACCTGGGCGAA[G/T]GATTCCAAATCAAAT | 55819 |
| rs189520962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179959015 | CAAGTGGAAATCTGC[C/G]TCCCTGTAGATATCG | 55819 |
| rs189556668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990895 | CTACAAACTAATGAT[A/T]AATGATATTCATATA | 55819 |
| rs189562352 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180060981 | GGCTGAGGCAGGAGA[A/G]TGGCGTGAACCCCGG | 55819 |
| rs189568823 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022952 | TGGGAGGAAAGTGGG[C/G]TACAGAAGCTTTCAC | 55819 |
| rs189578485 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179985496 | GGCCACTCTGAAGCC[C/T]TCAGTATTGAATTCA | 55819 |
| rs189610633 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179975364 | CTGTGTGTGGGTGGG[A/C]GCTACTGACACCTAG | 55819 |
| rs189623071 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063542 | ACTGAAGTAAAGATA[A/C]CAATAGGAAGCCAAG | 55819 |
| rs189643470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056612 | GAACCATGTTGGACA[C/T]GTTGGGCTTGAAAGA | 55819 |
| rs189654953 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180014342 | TCTATCAATCTATCA[A/G]CGATTGTCCTTTCAT | 55819 |
| rs189658155 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:180051968 | ACAGTGCAATATAAG[G/T]GTTAATTGTTTATCC | 55819 |
| rs189673599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011297 | GCCAGTTTTACAAAA[C/T]CCAAAAAAGGTCTAT | 55819 |
| rs189837844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973208 | CCAGAGATCTTCAGT[C/G]TCAAATTCCCATGGC | 55819 |
| rs189853795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942853 | TATGTGTAACTCTCT[A/C]CTGTGGATATAAGAT | 55819 |
| rs189868121 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017143 | TCCATTCATCACAAC[A/G]CTGACCTTTTTAAAG | 55819 |
| rs189870063 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994985 | GGGGACTGGTGGGGA[G/T]AGGTGAAGCTGGGTA | 55819 |
| rs189872191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997966 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA | 55819 |
| rs189890976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179963155 | GATGAGGATGCTGAC[A/G]GCCTTTTACACTCTA | 55819 |
| rs189891734 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180058648 | ACAACCTCTGCCTCC[C/T]GGGTTCAAGCGAGTC | 55819 |
| rs189909866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037202 | TCTGCTGTTACAATG[C/T]TGTAACACTCTCCTA | 55819 |
| rs189914354 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180032291 | ACTATCTTCTAAAAG[C/T]TTACAGTTTTACCTC | 55819 |
| rs189921944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002876 | GGAGGACAAGTTCTA[A/G]GGATTTCTAATGGGT | 55819 |
| rs189927954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179983114 | CAGATAAAAATCCTT[C/T]TGCATGTATTTCCCC | 55819 |
| rs189936546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062006 | TGGAGACTTCTTTGT[A/G]TCCTCACATGGCAGA | 55819 |
| rs189954115 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180021409 | ACCACAAGGTACATC[A/G]TTATGTATCATGAAG | 55819 |
| rs189958099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042094 | TAGATAAAGAGATGA[C/T]GCCAGTGGGAAAATG | 55819 |
| rs190081536 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179968173 | GGTGGCGGGTGCCTG[C/T]ACTCCCAGCTACTCG | 55819 |
| rs190095191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179921032 | GATTTTAAAATTCCA[C/T]AGTTACATTATTTGA | 55819 |
| rs190108327 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179972312 | GAAAAGTCACGGGGA[C/G/T]GCAAATGCCTAGTAC | 55819 |
| rs190123306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179958591 | GAACAGGTCTATCCT[G/T]TAGCTTCTGTCTGAA | 55819 |
| rs190127925 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179928851 | AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT | 55819 |
| rs190155054 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005472 | AAACCATATTGATTA[C/T]AGAATAAAGCCTAAC | 55819 |
| rs190161378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964353 | ACCTTTTCAGAGCCT[A/C]TGTTGTCAAGGTAAC | 55819 |
| rs190171350 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988041 | TTTCAGAAGAACTGA[C/T]GTTAATTCTCCTTTA | 55819 |
| rs190175391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970010 | AAAACAAAAAAGTTA[C/G]CCAGGCATGGCGGTG | 55819 |
| rs190186329 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179947630 | TGTAAAACGGAGTTA[A/T]TAAGAGGGTTGTTGC | 55819 |
| rs190192845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065964 | ATTTTACATATTGCA[A/G]ACTTTATAAAATTAT | 55819 |
| rs190200455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977326 | CAAGTCCCTGGAGTT[C/G]TTGTACCCAGAGCCA | 55819 |
| rs190229722 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179922211 | ACTAGTGACGTTGAG[C/T]ATCTTTTCATGGGCT | 55819 |
| rs190235410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943056 | AAAAATTAGTTGGGC[A/G]TGGTGGCACGTGCCT | 55819 |
| rs190289430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925987 | GGGGAGCAGCAGAGG[C/T]GAGGCAGGGAAGCAG | 55819 |
| rs190312017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962475 | GGACGTAATTGAATA[C/T]GGAGATCACGTGAAT | 55819 |
| rs190364850 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF130 | GRCh38.p7 | 5:180023252 | ATATGTAGATATGCA[A/G]GAGTTAGGATACACG | 55819 |
| rs190412108 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RNF130 | GRCh38.p7 | 5:179981535 | ATTACCAGTACTTTA[C/T]TTCTATTTTTCATCT | 55819 |
| rs190432020 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179951337 | ACACGATTAACTAGA[A/C]CTAACACACGTCTAC | 55819 |
| rs190446312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020305 | GGGAGCAGTGACAGG[C/T]GGGGAAGCACGTGAC | 55819 |
| rs190457916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180045467 | GGACCCAAACAGTGA[A/G]CAGCAGCAAGATTTA | 55819 |
| rs190460506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180049713 | AAAGGAGTCTCAACT[A/G]CCACGCTTAGTCTAT | 55819 |
| rs190551313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946518 | AGCGTTCTTCTTAGT[C/T]TTAACAGACCGACCA | 55819 |
| rs190602154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179967917 | TTTTTATGTTCATTA[C/T]ATTTAAGGATCCAAT | 55819 |
| rs190607852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975056 | GAGCGCCAGCCAGGC[A/G]GGGAGGCTCTGTCTT | 55819 |
| rs190611683 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | RNF130 | GRCh38.p7 | 5:179951545 | CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT | 55819 |
| rs190624170 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179930324 | GCCTCCCAGAGTGCT[A/G]GGATTACAGGCATGA | 55819 |
| rs190646514 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179982772 | TTATTTTTGTAGAGA[C/T]GAGGTCTCACTATGT | 55819 |
| rs190671009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179967059 | AGGAAAACACAACCT[C/T]TCATAAGATTCTAAA | 55819 |
| rs190680816 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNF130 | GRCh38.p7 | 5:179930215 | GGCATCTGCCACCAC[A/G]CCCGGCTAATTTTTG | 55819 |
| rs190686993 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071101 | CCTGCCGCTTCCAAA[A/C]TACAGGCTGAGACGT | 55819 |
| rs190700277 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001414 | GTGGCACCTGTGGCA[A/C]AGTGGGATATGTTAC | 55819 |
| rs190704463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027395 | CTTCTCTGAGTATAA[A/G]CAGAAACAGAAAGGC | 55819 |
| rs190705947 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180021688 | TCATATAAAAACTTT[C/T]AAAACCTAGAACCAT | 55819 |
| rs190797688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030903 | CCAGTGTGAACTGTC[C/T]AGATCCACTTACAGG | 55819 |
| rs190802309 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012904 | ATTTTAAATATCCCT[G/T]AAATACTCATGTAGA | 55819 |
| rs190824783 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180054006 | ATTTTTAGCAGAGAT[A/G]GGGTTTCACTATGTT | 55819 |
| rs190837155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989046 | AAGAAAAGAGGTTTA[A/G]TCAACTCAGTTCCGC | 55819 |
| rs190845234 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180034836 | ATGGGGACCCCAGAC[A/G]TAGTTACCATAAAGT | 55819 |
| rs190849609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179970843 | AGTTATGCTTTCTAC[A/G]ATAGCTAACATAGAA | 55819 |
| rs190857654 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179957356 | GGCAGAAGTTGCAGT[A/G]AGCCGAGATCCCACC | 55819 |
| rs190874008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057491 | AGGTGGAGGCTGCAT[C/T]GAGCCAAGACCGTAC | 55819 |
| rs190878070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180025522 | AAAAGAAAATTAAGA[A/G]CTTATGGAAGTTTTA | 55819 |
| rs190882291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180008185 | AGCAGCCCACCACCC[A/G]ACCCCAGAAAAAGCC | 55819 |
| rs190909744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180006509 | TATAAAGTCAAAGAA[C/T]ATTATATACACATGT | 55819 |
| rs190915670 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065539 | GCCGAGACAGGCGGA[C/T]CATGAGGTCAGGAGA | 55819 |
| rs190916485 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179937812 | AATGTCCATCAGTGG[A/T]TGAGGAGATGAACAA | 55819 |
| rs190924019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179970151 | CAGAGTGAATCCTTG[C/T]CTCTTAAATTTAAAA | 55819 |
| rs190931334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180047537 | ATCACCTGAGGTCGG[A/G]AGTTCAAGACCAGCC | 55819 |
| rs190938229 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042986 | TAAAGATTTAGATAG[A/T]CTTATCTCACAGAAT | 55819 |
| rs190958776 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073787 | TAATCTGGTCCCCTC[C/T]AGCTGGACCCTTCAT | 55819 |
| rs191004824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939419 | TTCAAAAAAATGTTC[C/T]TGTTAACCCTCAGAT | 55819 |
| rs191056190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944283 | CTTATTTCTAATAAA[C/T]TTTAAGTCCTAAGTG | 55819 |
| rs191088269 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179991937 | ATGCTTTGCATGTAC[A/G]GTTCACAGTAGGCTT | 55819 |
| rs191092336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974041 | GCTGCGGGAGGGGAG[A/G]CCTCTATATTGAAGG | 55819 |
| rs191104421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960390 | AAACAGTATTTCATC[A/G]TAACAGAAGGGCAGT | 55819 |
| rs191112460 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030392 | AGGTATAATTTACAT[C/T]CTACAAGACTCATCT | 55819 |
| rs191130737 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180011611 | CCTGTGCAAAAAAAT[A/T]AAAAAATTAGCCAGT | 55819 |
| rs191132024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956333 | GAGCTCCAGATCTCT[A/G]CTTCAAACCATATAA | 55819 |
| rs191138706 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179931392 | CTGTGTTCTTTTGTG[C/T]GTGTGCTTTAAGTGT | 55819 |
| rs191158001 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988579 | CTTTTGCTGTATCTT[G/T]TAGGTTTTGGTATGT | 55819 |
| rs191183362 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013936 | ATGGTGCCACCTTTT[A/G]TTAGTGACATCTGAA | 55819 |
| rs191185559 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180067364 | ATGTTACATATGCCA[C/T]GTCTTCATCAAAATC | 55819 |
| rs191189757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024296 | AAAGTAATAGACTTT[G/T]GTTAATAATTATGTA | 55819 |
| rs191199306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993631 | TGGATATTAGCCCTT[C/T]GTCAGATGGGTAGAT | 55819 |
| rs191204751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974840 | GAGCAGGCACGCAGC[A/G]GCGCGGGGAGGAGCG | 55819 |
| rs191212650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055363 | CACCATGCCCAGCTA[G/T]AAGTAAGTTAAGTTT | 55819 |
| rs191216327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955847 | AGTTTCAGATCTGCA[A/G]TTGACTGACTCATCC | 55819 |
| rs191221199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031709 | ACAATGCTGCTATGA[G/T]CATTTGTGTGTAAGT | 55819 |
| rs191271925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016548 | CACTTCCACGTCTGG[C/T]CGCCAGTACTAACTG | 55819 |
| rs191300592 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180054768 | GTCTGAATGTGTAGG[A/T]CAATTTGGAGGGCAC | 55819 |
| rs191393118 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948544 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 55819 |
| rs191401598 | snp | A/G | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920269 | GAAAGGTGATCAGAA[A/G]TCAAATCACAAAAGC | 55819 |
| rs191406975 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179951607 | CCAGGATGGTCTCGA[A/T]CAGAATATGTACATT | 55819 |
| rs191410491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179964673 | TTCTAGAAAAACATA[C/T]TTTTGTTAGATTTTA | 55819 |
| rs191429453 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179937490 | AATGCAAATCAAAAC[C/T]ATGATGAAATGCCAT | 55819 |
| rs191450264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978543 | AAAATTAAGTCGGAA[C/T]TCTAATTTTTTCCAG | 55819 |
| rs191458548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179941004 | TCTCTATTGAGTTCT[C/T]CCTTTCAATTATTTT | 55819 |
| rs191488706 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179962060 | TCTTACAACTGAAAA[A/G]CGGAGGAGCTGAGAG | 55819 |
| rs191498582 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057885 | CAAGACAGATGTGTG[G/T]GTACCCTTTGTCCCA | 55819 |
| rs191509202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179945106 | ACATGGTTAAAAAAA[C/T]AAAGTGATAACTGAC | 55819 |
| rs191510684 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | RNF130 | GRCh38.p7 | 5:179997196 | GCCCAGGCTGGAGTG[C/T]AGTGGCGTGATCTTG | 55819 |
| rs191635147 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179985247 | GAAATCATGTACTAC[A/G]TCTGGACACAGTTTT | 55819 |
| rs191648800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925036 | AAGCTATCTGCCATA[C/T]TGTGAAAAGTGTATT | 55819 |
| rs191659568 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180022481 | AGTGTCTTCACTTAC[A/G]TAAATGTGAACTACA | 55819 |
| rs191671349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004204 | CTTTTGTATACTAAA[A/G]TTTGAGACTCACTAA | 55819 |
| rs191689246 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064085 | TATGAGCTAGGCAAC[A/G]TAGGACCTATTATAA | 55819 |
| rs191691537 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179944548 | GGCTCACTGCAACCT[C/T]CACCTTCCGGGTTCA | 55819 |
| rs191723181 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974342 | CACTCCGATGGCCGA[C/T]CTTTAAGAGGTCTAA | 55819 |
| rs191729772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001809 | GATAATTCCACTCTC[C/T]AAGAGGAAGGTTATC | 55819 |
| rs191753012 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180035693 | CTCTGATATATGTTG[C/G]TGTGTCTGACAGTGT | 55819 |
| rs191753199 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180041316 | TCACCCCACAACTCC[A/G]TATCAAGATACACTT | 55819 |
| rs191810701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996910 | CTCTTCTTTAAATGT[A/T]TGGCAGAATTCTGCA | 55819 |
| rs191835759 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179929963 | CTCTGTATAAAAGCC[C/T]TGCGTATCTTCTCTT | 55819 |
| rs191842726 | snp | A/G/T | 0.00597646 | 0.0543919 | intron-variant | RNF130 | GRCh38.p7 | 5:179950082 | AATCTCATTATTTAA[A/G/T]GTTGACAGTTGATAG | 55819 |
| rs191847445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068319 | CCATTTGAGTAAGTA[A/G]TAAGAAAGCAACCGT | 55819 |
| rs191956000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179963893 | TAGATTTTTTTCATT[A/G]TTAATGTAAATGACA | 55819 |
| rs191962328 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179928428 | TTAACGTCCATTCCC[C/T]AAATGACCAAAAAGG | 55819 |
| rs192007538 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179952606 | ATCCTCAGCAAAATA[C/T]TAACAAACTAAATCC | 55819 |
| rs192008017 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180020949 | GTCCACAGGTCACCT[G/T]GATTTAAGTCTTAGG | 55819 |
| rs192022649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179961611 | CTCGAAAAGTGCCTA[A/G]TGTAATTATTTGCTT | 55819 |
| rs192027056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922859 | GGATCGCTTGAGTCC[A/G]GGAAGCAGAGGCTGC | 55819 |
| rs192029403 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053137 | CAACTGGCCAAATGG[A/C]GTAAAGATAAAGGTT | 55819 |
| rs192036236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983952 | TAGGGTCTTGTTATG[C/T]TGCCCAGGCTGGACT | 55819 |
| rs192038556 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180061589 | CCATCCTTTGCACCC[A/G]CCGGTTTGTGGCAGA | 55819 |
| rs192056593 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992505 | AGTATTTCATTTCCA[A/G]GAGTTGTCTGTTTTT | 55819 |
| rs192059148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000144 | GAAAGACTATTTCAC[C/G]CCCATTTCTGAAGGA | 55819 |
| rs192070117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025964 | CTTGTTTTCATAAAG[C/T]ATTTTTTGTATTCAC | 55819 |
| rs192070440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980854 | GACACTGCTAGCACT[A/G]CTTGGCACCAACAAC | 55819 |
| rs192074766 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180008838 | GCAGTGAGCTGAGAT[C/G]GTATCACTGCACTCC | 55819 |
| rs192096863 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180056124 | AAAACAAACAAACCA[C/T]CACCACCAATCAGAT | 55819 |
| rs192101864 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069052 | CAAGTATTCCAATTT[G/T]AAATCATTTTCTTAA | 55819 |
| rs192118123 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180032204 | AAGGTTTTTAATTTT[C/G]ATAAAATCTAATTTT | 55819 |
| rs192121251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180047925 | AACCTTCAATACTGA[C/T]GCTCCCGAGTACTCT | 55819 |
| rs192241846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947016 | CAACACCTCTCTCCC[G/T]GAGGATGCACTGTTG | 55819 |
| rs192270572 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179977039 | TCCTTTCCTCATGGA[C/G]GAAGGCTTGGTCCCA | 55819 |
| rs192276105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932699 | AAAAATTAGCCAGGC[A/G]TGGTGGCACATCTGT | 55819 |
| rs192287643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065588 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAACTA | 55819 |
| rs192312881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179984476 | ATCGATGTTGGACTT[C/T]GGCAAATATCTTTTC | 55819 |
| rs192321004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968614 | GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG | 55819 |
| rs192334165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180049645 | TTTAATCCTATTTAC[C/T]CCTGCACTTAACACT | 55819 |
| rs192343334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003920 | TCTATACTAACTAAG[G/T]TTTATTCGGTACATA | 55819 |
| rs192358907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059178 | GCACCTTTTAGTCTT[C/T]GTGTATATTTCCTTG | 55819 |
| rs192360897 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180010059 | GAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC | 55819 |
| rs192361080 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990385 | CAAAGACTTTAACAC[G/T]TTCACTAATTTTGCT | 55819 |
| rs192369365 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972271 | AAACTCCCTTAGATC[C/T]GATAGAAGTTACAGA | 55819 |
| rs192372929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003536 | TGGACTTGGCTTCAG[C/T]ATTACTACCTTCTTC | 55819 |
| rs192388773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180027954 | ACCTCATCGAGACCA[C/T]GCCTCCCTTCTTTCA | 55819 |
| rs192392368 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | RNF130 | GRCh38.p7 | 5:179968498 | TGGGGAAACCCCATC[G/T]CTACTAAAAACACAA | 55819 |
| rs192393407 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180049884 | TTTTCCTCATCTATA[G/T]ATTCAAGTTCTATTT | 55819 |
| rs192476016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972003 | AACCAGAACCATCAC[A/C]CCTGAAGGCATTTAT | 55819 |
| rs192506025 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008969 | GGGTAAAAGAAGAAG[A/T]CTCAAAAGAAAAAAA | 55819 |
| rs192552989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031409 | GGAGAATTGCTTGAA[C/T]CCAGGAGGCGGAGGT | 55819 |
| rs192554860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969045 | AAAATAAGATGACTT[C/T]GATCTCCTTTGGGTT | 55819 |
| rs192562280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993344 | CAGTCCCACCAACAG[G/T]GTAGAAGTGTTCCTA | 55819 |
| rs192563232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179946337 | CCCCACAGGGAGGGC[C/T]CGCGTCAGGCCCCCC | 55819 |
| rs192568457 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179934920 | TTTATTTCCTTCCTT[C/T]GATTTAGTTTGTTGT | 55819 |
| rs192584347 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179962201 | GTGCAGTGCTCCTCT[C/G]AAGGCTGGGGAATGC | 55819 |
| rs192691982 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044950 | TGAAGGAGGGAGGAG[A/G]GCAGGACGATGGTCA | 55819 |
| rs192715827 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180070152 | CATTGTTAGTTGCCA[C/G]TCTGGCAACACTGTG | 55819 |
| rs192744320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989464 | AATATTTTGAATTGT[C/T]ATATCCTCCTGCAGA | 55819 |
| rs192750711 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179957679 | GTCACTCAATCCCTC[A/G]AAGCCCTACTTTATT | 55819 |
| rs192768263 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179929172 | AATTAAGATTCATTT[C/T]TTTCTTTATAAATAT | 55819 |
| rs192807146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027018 | GTAAGGGCAATGATC[C/T]GGGTTTCTCTCCTTT | 55819 |
| rs192814231 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179989954 | TGTTTCCATGTCTGG[G/T]ACTCCTTTGAGCCTC | 55819 |
| rs192815208 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179974561 | CTTGACAGCTCTGGA[C/T]AGAAAGTCCTAGCTG | 55819 |
| rs192831482 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180013487 | GGCACCAAGTAGGAA[C/T]ATGTAATTTGTTGTG | 55819 |
| rs192837070 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954351 | CAAGTCAAGCGTCCA[A/T]CAGCAGAACAAAATG | 55819 |
| rs192870538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059926 | AACTAGGTTGCAGAT[C/G]AAACAAGGTTGATCA | 55819 |
| rs192872847 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018818 | GTGAGTCTACCCAGC[G/T]GGGAAGAGTCTGATC | 55819 |
| rs192913266 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180014125 | CAGAGGTCTGCCCAC[A/G]AGCACAGGCTATGCA | 55819 |
| rs192953719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971725 | TGGTATATACCTTTA[C/T]AACTTTGATTGTCAA | 55819 |
| rs192961068 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939963 | GTCCCTTTTTTTTTT[C/T]TCTAGCATCAGACAG | 55819 |
| rs192990161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180044232 | CAACTTTTATAAGAG[A/G]ATACTATCTCTGAAT | 55819 |
| rs192997337 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179946540 | GACCGACCAGTACAG[A/C]ACACCCACCGGGGAT | 55819 |
| rs192998103 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179975224 | GAAGGAATTCTGTAA[G/T]CGGCAGTTTGGTGAG | 55819 |
| rs193015545 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179999444 | TGAAGTGAGTTGGCC[G/T]GCCATGGTGGCTTAC | 55819 |
| rs193018571 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179929382 | AGTCTTGATTTCCAG[C/T]ATCTAAGTCCTTTTG | 55819 |
| rs193026785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966054 | ATGAAAGGAACATGT[A/G]GAGAATGGAAGCGAA | 55819 |
| rs193036814 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180038208 | TACAGGAATGCACCA[C/T]CACACCTGCTAATTT | 55819 |
| rs193044638 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072550 | GCACTGGGGGACGGG[C/T]TTCCAGGAAGAGAGT | 55819 |
| rs193073401 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180038801 | TACTTCTCTGTGGTT[C/T]TGTGTAAGTAAAACA | 55819 |
| rs193111542 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179925772 | CCCTGGGCTTAAGCC[A/G]TCCTCCCACCTTGGC | 55819 |
| rs193158860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063863 | GTAAATACAAAATTA[C/T]TTTTGGAAGACAGAG | 55819 |
| rs193191934 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179962605 | GATATCCTCAGTAAA[C/T]GTCCAAAATTTAGAA | 55819 |
| rs193199991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926518 | GCCGGGTGTGGTGGC[A/G]CATGCCTGTAATCCC | 55819 |
| rs193200750 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179994192 | TCTTTTGGCTTATGC[A/G]GGCTCTTTTTTGGTT | 55819 |
| rs193202122 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180021833 | GTCACTGCCATCCAA[A/T]CCCGAAGTCCATCCA | 55819 |
| rs193213522 | snp | C/T | 9.88598e-05 | 0.00702995 | intron-variant | RNF130 | GRCh38.p7 | 5:179980101 | GCTGGATTACTTTTA[C/T]GGTGCTGAAGTTGTT | 55819 |
| rs193214739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949806 | TTCAGAAATGCTGTA[A/G]ATAATTAAGACCAGA | 55819 |
| rs193221818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018168 | GGTGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 55819 |
| rs193275102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179932361 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTCCCTCAG | 55819 |
| rs199516849 | in-del | -/TTAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049781 | TATTTTATTGTGTTC[-/TTAT]TTATTCTACTTTTCT | 55819 |
| rs199520821 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015446 | AAGACTCAAGCTGGA[-/A]AAGGAGTAGGGAAAG | 55819 |
| rs199541530 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense | RNF130 | GRCh38.p7 | 5:179963492 | GCATTCAAGCTAGCT[G/T]TGGCTCTGATGATCA | 55819 |
| rs199655631 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015749 | AGGAAAAGGAGTAGG[A/G]AAGGAGTAGGGAAAG | 55819 |
| rs199715834 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036846 | CCCCACACTCAGCTT[A/G]AGAAATAAAACATTA | 55819 |
| rs199722362 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993127 | TCCAGTCTATCGTTG[C/T]TGGACATTTGGGTTG | 55819 |
| rs199736398 | snp | A/G | 0.00199792 | 0.0315431 | missense | RNF130 | GRCh38.p7 | 5:179966877 | AGAGGTGAGATCCCC[A/G]AAGTTCGAAGTGGCT | 55819 |
| rs199781115 | in-del | -/TGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998884 | ATATATATATATATA[-/TGTTT]TATATATCTGAGTGC | 55819 |
| rs199814663 | in-del | -/G/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038410 | AAAAAAGCCTGTTTT[-/G/TG]GTTTTTTTTTTTATT | 55819 |
| rs199855040 | in-del | -/CAGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028561 | CTTCCAGACCTGGGT[-/CAGA]ACCCCTTTCGTAATA | 55819 |
| rs199864103 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051269 | TTATTTATTTATTTG[A/T]GACAGAGTCTCGATC | 55819 |
| rs199877632 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036849 | CACACTCAGCTTAAG[A/T]AATAAAACATTATAG | 55819 |
| rs199881538 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065812 | AAACACAGAAAAAAA[A/T]GTTTCCTTCCTTTAT | 55819 |
| rs199888512 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047012 | TTACCACGTGAAACA[C/G]AGAACTCTTTGCCAC | 55819 |
| rs199911451 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016341 | GAGCTCTGGCCCAGT[C/T]TCACGCCAAAGGAAA | 55819 |
| rs199916750 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:180051960 | TTGGTGTCACAGTGC[-/A]ATATAAGTGTTAATT | 55819 |
| rs199939686 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944576 | TCAAGCAATTTCTCC[C/T]GCCTCAGCCTCCTTG | 55819 |
| rs199980621 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982571 | GTGAGATTTTGTGTT[G/T]TGTTTTGTTTTGTTT | 55819 |
| rs199994496 | snp | C/T | 0.000399281 | 0.0141238 | missense | RNF130 | GRCh38.p7 | 5:179966997 | GCTACGTTATCAGTA[C/T]ATGGCAAATTCGGCT | 55819 |
| rs199997674 | in-del | -/AT | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179973832 | CGGAAAGCAGGTAAC[-/AT]GTGGACAGTGAAACC | 55819 |
| rs199999821 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937929 | GTGTGTGTGTGTGTG[A/T]GTGTGAGAGAGAGAG | 55819 |
| rs200007053 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033776 | ATTCTTTCAAGACTT[A/G]TTTATTACATCTAGT | 55819 |
| rs200022291 | in-del | -/AT/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065811 | AAACACAGAAAAAAA[-/AT/T]TGTTTCCTTCCTTTA | 55819 |
| rs200032600 | in-del | -/TGT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974832 | AGGGAGAGAGCAGGC[-/TGT]ACGCAGCGGCGCGGG | 55819 |
| rs200040320 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942166 | TTAGAACCATCTCAG[A/T]ATGAAATAAAGAGGG | 55819 |
| rs200068075 | snp | A/C | 0.000101191 | 0.00711232 | intron-variant | RNF130 | GRCh38.p7 | 5:180040434 | AAAAACAAAATCAAC[A/C]ACCCTCATTTTTGTT | 55819 |
| rs200135699 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064933 | TCCACTTACTTCTCT[A/C]TAGGATTCACAAACT | 55819 |
| rs200144083 | in-del | -/A/AT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179920796 | TATATATATATATAT[-/A/AT]TTTTTTTTTTGAGAT | 55819 |
| rs200189227 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011491 | ATATACAAAGGTTGA[G/T]GGTGGTGTTCACACC | 55819 |
| rs200193970 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937939 | GTGTGTGTGTGAGAG[A/T]GAGAGAGAGAGAGAG | 55819 |
| rs200199687 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019173 | GTGGATCACCAGGCC[A/G]GAAGATCAAAACCAT | 55819 |
| rs200205272 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985456 | GCTCTAGAGGTTGAA[C/T]TAGAGGCATGTCTGG | 55819 |
| rs200212903 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045846 | CTAGACACAGAGTGC[C/T]GATTGGTGCATTTAC | 55819 |
| rs200215989 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053842 | TTTTTTTTTTTTTTT[A/T]AATTTGAGACAGAGT | 55819 |
| rs200293649 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992594 | TTACTGTGTTTTTTT[-/G]GGGGGGGTGTCATAT | 55819 |
| rs200311237 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927345 | TGTTATTGGCTACAT[A/G]ATGTTATTAAGTAAA | 55819 |
| rs200346337 | in-del | -/TGT | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179945273 | CCACACCCTGCAGGG[-/TGT]GCTGACTGCACCTGG | 55819 |
| rs200391151 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931071 | AATCAAGAATAGGTG[C/T]TGAATTTTAGCAAAT | 55819 |
| rs200406287 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036847 | CCCACACTCAGCTTA[A/C]GAAATAAAACATTAT | 55819 |
| rs200436383 | snp | A/C/G | 2.36454e-05 | 0.00343833 | intron-variant | RNF130 | GRCh38.p7 | 5:179963447 | CATCTGGCACATGCA[A/C/G]TCCAAAAACAATTTG | 55819 |
| rs200507014 | in-del | -/GAAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015736 | GTAGGAAAGGAGTAG[-/GAAAAGGAGTA]GGAAAGGAGTAGGGA | 55819 |
| rs200519143 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015714 | AGGGAAAGGAGTAGG[A/G]AAAGGAGTAGGAAAG | 55819 |
| rs200523891 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994856 | ACAGTTCTAACAGTA[A/G]GGTTTACGACTTATC | 55819 |
| rs200542408 | snp | A/G | 9.9691e-05 | 0.00705943 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013073 | CACCTGGTTCCTGTC[A/G]CGTGCATTTGTGTAC | 55819 |
| rs200566563 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028565 | CAGACCTGGGTCAGA[A/C]CCCCTTTCGTAATAA | 55819 |
| rs200572987 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969642 | GGAGGCTGAGGCAGG[A/T]GGATCACTTGAGGCC | 55819 |
| rs200589829 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047010 | TTGTGGCAAAGAGTT[C/T]TCTGTTTCACGTGGT | 55819 |
| rs200690438 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016342 | AGCTCTGGCCCAGTT[A/T]CACGCCAAAGGAAAT | 55819 |
| rs200691698 | in-del | -/TTAT | 0.0174175 | 0.0916809 | intron-variant | RNF130 | GRCh38.p7 | 5:180000585 | CATTATTTTTCATTC[-/TTAT]TTCTTTTTTTTTGTC | 55819 |
| rs200694139 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024450 | TTCTAAAAAGTAAAG[-/T]TTTTTTTTTAAAGAC | 55819 |
| rs200761679 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942168 | AGAACCATCTCAGTA[A/T]GAAATAAAGAGGGCA | 55819 |
| rs200771730 | snp | A/G | 6.72269e-05 | 0.00579732 | intron-variant | RNF130 | GRCh38.p7 | 5:179978320 | AACAAAAAGTCACAC[A/G]CTGCAAGTATATAAA | 55819 |
| rs200792842 | snp | A/G | 0.00498743 | 0.0496874 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015234 | CAATCACAAAATAAT[A/G]CTAAACCGCTTTAAA | 55819 |
| rs200798739 | in-del | -/TG | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:180065754 | GACAGAGTGAGACTC[-/TG]TCTCAAAAAAAAAAA | 55819 |
| rs200806901 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051238 | TTTTGTATAGATATT[A/T]TATTTATTTATTTAT | 55819 |
| rs200809956 | in-del | -/C | 0.0123378 | 0.0775674 | intron-variant | RNF130 | GRCh38.p7 | 5:180050588 | ATTCACCATCACAGT[-/C]CTCCTCACAGCTCAC | 55819 |
| rs200817955 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932215 | AATTGTAATTTTAAG[-/T]TCCATGTGTTTAATC | 55819 |
| rs200832547 | in-del | -/CATA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051936 | TTAGAGCTTGGTCCT[-/CATA]CAAAGTTGGTGTCAC | 55819 |
| rs200847743 | in-del | -/AAAG | 0.0260105 | 0.111035 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073554 | TCTCAGAAAAAGAAA[-/AAAG]AAAGAAAACAGATGT | 55819 |
| rs200884753 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019384 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55819 |
| rs200958427 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974952 | GGCAGTCAATGGTGA[A/C]GCGGTCCTCTGAGAG | 55819 |
| rs200965887 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053824 | AAAAAGCAAATACAT[-/TC]TTTTTTTTTTTTTTT | 55819 |
| rs200989380 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055441 | AATGTCAGATGACTT[C/T]GTGTGTGTGTGCGTG | 55819 |
| rs201086996 | in-del | -/TGTTTTGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982567 | TATGGTGAGATTTTG[-/TGTTTTGTTT]TGTTTTGTTTTGTTT | 55819 |
| rs201097064 | snp | A/G | | | missense | RNF130 | GRCh38.p7 | 5:180071590 | ACCGTCACGTTGATG[A/G]GCGCCGTGTAGTACT | 55819 |
| rs201118376 | snp | A/C/T | 0.00417314 | 0.0454889 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071592 | CGTCACGTTGATGAG[A/C/T]GCCGTGTAGTACTCC | 55819 |
| rs201121243 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065217 | TCCCCCTGTCCTTTC[A/C]TGGAAAATTTTCCCC | 55819 |
| rs201173714 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053844 | TTTTTTTTTTTTTTA[A/T]TTTGAGACAGAGTCT | 55819 |
| rs201198419 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043113 | ACTCAAGGCCAGGAG[G/T]TCAAGACTAGCCTGG | 55819 |
| rs201202900 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964914 | ATTCAAAAACACATA[A/T]AAAACCCACCATTTT | 55819 |
| rs201235075 | in-del | -/CTAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034597 | TAGGAATTTGTTCAT[-/CTAA]GGTGTCTAATTTGTC | 55819 |
| rs201265884 | in-del | -/TTTTTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033156 | TTTTTTTATTTTTTA[-/TTTTTTT]GTAGAGACAGGGTCC | 55819 |
| rs201298471 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018295 | GTGAGACTCCATCTC[A/C]AAAAAAAAAAAAAGA | 55819 |
| rs201321947 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968019 | TTAACAAACAGGCTG[G/T]GCGCGGTGGCTCACG | 55819 |
| rs201366649 | snp | C/G | 0.00012022 | 0.00775212 | intron-variant | RNF130 | GRCh38.p7 | 5:179966797 | GCCTGAGCGGAGGCC[C/G]CCACTTACTTGTTAC | 55819 |
| rs201370600 | snp | A/T | 2.38143e-05 | 0.00345059 | intron-variant | RNF130 | GRCh38.p7 | 5:179963446 | TCATCTGGCACATGC[A/T]ATCCAAAAACAATTT | 55819 |
| rs201371560 | in-del | -/G | 0.0267878 | 0.112589 | intron-variant | RNF130 | GRCh38.p7 | 5:180038386 | ACCCTGTCTCGGGGA[-/G]GGGGAAAAAAAAAAA | 55819 |
| rs201375232 | snp | A/G | 1.6476e-05 | 0.00287014 | stop-gained | RNF130 | GRCh38.p7 | 5:179978219 | TGCAGGGGAGAATTC[A/G]GACGACATCATTCTG | 55819 |
| rs201415698 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034597 | TAGGAATTTGTTCAT[A/G]TAAGGTGTCTAATTT | 55819 |
| rs201444343 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020258 | GTGGATTCTCAAGTT[A/G]CCCAGGATGGTGGCA | 55819 |
| rs201469458 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928285 | GTTCCAAAGTGGCTG[A/C]GCCAACTTTGACTCC | 55819 |
| rs201475396 | snp | A/G | 0.0425132 | 0.13946 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071529 | AAGCCCGTAGCGCCC[A/G]CGGTCGATGCGAAAC | 55819 |
| rs201482706 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028566 | AGACCTGGGTCAGAA[A/C]CCCTTTCGTAATAAC | 55819 |
| rs201556584 | in-del | -/TTGT | 0.151668 | 0.229849 | intron-variant | RNF130 | GRCh38.p7 | 5:179993569 | CACTTTTTGATGGGG[-/TTGT]TTGATTTTTTTCTTG | 55819 |
| rs201562433 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065773 | TCAAAAAAAAAAAAA[-/C]AACTATGTAAAGAAA | 55819 |
| rs201581074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180056254 | ATAGTATCTGTGGGG[A/G]AAAAAAAAAAAACCC | 55819 |
| rs201586445 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942165 | CTTAGAACCATCTCA[A/G]TATGAAATAAAGAGG | 55819 |
| rs201588543 | snp | A/G | 0.000120334 | 0.0077558 | intron-variant | RNF130 | GRCh38.p7 | 5:179970406 | AATAAAATAGGAAAC[A/G]TACCACAATTCCCAG | 55819 |
| rs201595061 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997808 | ATTTGAACTTCATTA[-/T]TTTTTTTTTGCTTCT | 55819 |
| rs201609191 | in-del | -/CAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927342 | CTTTGTTATTGGCTA[-/CAT]AATGTTATTAAGTAA | 55819 |
| rs201677542 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021501 | TGAGCATCCCAGAAC[-/TG]CAATGAGAATTCTTC | 55819 |
| rs201726993 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055440 | GAATGTCAGATGACT[G/T]TGTGTGTGTGTGCGT | 55819 |
| rs201730023 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180025878 | TAGAATAAAGAAAAT[A/C]GATTTACGTTAAGTG | 55819 |
| rs201731057 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034590 | ATATTTTTAGGAATT[A/T]GTTCATCTAAGGTGT | 55819 |
| rs201741513 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993126 | ATCCAGTCTATCGTT[G/T]TTGGACATTTGGGTT | 55819 |
| rs201745904 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958172 | GTGAGCCACCGCGCC[C/T]GGCCAAATTCAAAAT | 55819 |
| rs201767062 | snp | A/C/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179968823 | CTGTCGTGGCTGTGG[A/C/G]GCCATGCTACTAGCA | 55819 |
| rs201799021 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956155 | GCATCAGGTGTAAAA[G/T]CAGCCTATGACCTTT | 55819 |
| rs201841326 | in-del | -/ATG | 0.0287284 | 0.116357 | intron-variant | RNF130 | GRCh38.p7 | 5:180024590 | ACCTGTCTTTGAAAA[-/ATG]ATGATGGCCAAAAAA | 55819 |
| rs201855223 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033697 | CGAGACTCTGCCTTT[A/T]AAAAAAAAAAAGAGA | 55819 |
| rs201911148 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064142 | AGCCTATTTATGGAA[-/T]AAAATCAATTTAACA | 55819 |
| rs201925862 | snp | C/T | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:180040533 | TTGTGGAAAGCGGCC[C/T]GTGATATTTTCTCTT | 55819 |
| rs201962809 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051268 | TTTATTTATTTATTT[A/G]AGACAGAGTCTCGAT | 55819 |
| rs202016265 | in-del | -/CATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988609 | TTTTATTTCCATTTT[-/CATT]TATTTCAAGAACTTA | 55819 |
| rs202040162 | in-del | -/TTTTCT | 0.0119091 | 0.0762411 | intron-variant | RNF130 | GRCh38.p7 | 5:179971103 | GGGGAGGATGGGAGA[-/TTTTCT]TTTTCTCTCTTATTC | 55819 |
| rs202063179 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937937 | GTGTGTGTGTGTGAG[A/T]GAGAGAGAGAGAGAG | 55819 |
| rs202093486 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054901 | TATTACTTTAAATGA[C/T]ATTGTGAAATTTTTA | 55819 |
| rs202101833 | in-del | -/TA | 0.486398 | 0.0813386 | intron-variant | RNF130 | GRCh38.p7 | 5:179998860 | AGATCTAGTATTTTT[-/TA]TATATATATATATAT | 55819 |
| rs202135338 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028120 | TTCCCCACCTCAGAT[C/T]CTTCACTTACAAGGG | 55819 |
| rs202177344 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937158 | TATCATCAAAACGAA[A/G]TATCATCAAAACGAA | 55819 |
| rs202200962 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953125 | AAAAAAATATGAGAA[C/T]AAATGAGTTCAGCAA | 55819 |
| rs202214188 | snp | C/T | 6.59033e-05 | 0.00573997 | missense | RNF130 | GRCh38.p7 | 5:180013219 | GAGTTCCAACAGCTA[C/T]TGTCATTTGTACAGA | 55819 |
| rs367551468 | in-del | -/AAGAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951310 | GAAGAAAAACAAGAT[-/AAGAT]TTGAGCAACACGATT | 55819 |
| rs367558228 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045953 | CCGTGCGGCATGCCC[A/G]CACTCCTCAGCCCCT | 55819 |
| rs367566877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066303 | TAATTTTCTCTTGCT[A/G]CCGCCATGTAAGAAG | 55819 |
| rs367585881 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | RNF130 | GRCh38.p7 | 5:179961897 | CAGTGGCATTGGCTT[A/C/G]GCTAACATTTATTGA | 55819 |
| rs367590467 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937177 | CATCAAAACGAAGTA[C/T]CATCAAAACGAAATA | 55819 |
| rs367590940 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009554 | ACACAACTCAACAAT[C/T]ACAAGAGATGAAAAC | 55819 |
| rs367600473 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973695 | CCATGGACACCCAGG[A/C]GGCCTCAGAAAGAGG | 55819 |
| rs367606385 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000636 | AAATAACCTATCTTC[A/C]AGTTGAGAGATTCTT | 55819 |
| rs367630111 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013169 | TATTGACACGAAGAC[C/T]AGAGAGCCACGGCTG | 55819 |
| rs367704518 | snp | A/G | 1.65864e-05 | 0.00287974 | intron-variant | RNF130 | GRCh38.p7 | 5:179955693 | TAAAAGGAAAAAAGA[A/G]GTCATAAATTAAAGA | 55819 |
| rs367721567 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959144 | AGACCAGTGCAGGAC[G/T]AAGATCTTGGTAGGC | 55819 |
| rs367728987 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955786 | AGCTAGTTCCCAACC[C/T]CTCTGGTAAGGCCAG | 55819 |
| rs367739135 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986413 | GCACTATGGCACTTC[A/G]TACAGGTCCCATGGT | 55819 |
| rs367750315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931629 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGCCTGCC | 55819 |
| rs367754351 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967284 | GTCATGGCCCACAGG[C/T]ACAGGGAGTCGTAAT | 55819 |
| rs367755100 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979754 | ATTGTAAAGAGAGCA[C/T]CTTTTTAGGTGAAAC | 55819 |
| rs367766596 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923792 | TCTTGCTCAATTAAA[A/C]TCTGTTAAATTTAGT | 55819 |
| rs367823885 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016899 | CCACGGTCCCTCCTA[A/C]GAACAAGGCTAGCTA | 55819 |
| rs367825792 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028393 | TCTACTTGCAGTTAC[C/T]TGATTTTCTCCATTT | 55819 |
| rs367827085 | in-del | -/AG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032230 | ATTTTTTTTATAAAC[-/AG]TGTTTTTGGAGTTAT | 55819 |
| rs367869076 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960845 | CAGGGCAATTAAGGT[G/T]AAAAAAAAAAAAATC | 55819 |
| rs367873718 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047773 | ATAAATCTCAGGCCA[C/G]TCTTTGTTCTCCAAA | 55819 |
| rs367888142 | snp | A/C | 0.000153988 | 0.00877328 | missense | RNF130 | GRCh38.p7 | 5:180013303 | TGACAGCAATAATAT[A/C]TCCAGTGCCTGCAAT | 55819 |
| rs367917088 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986529 | ACCTAATGGAGGGAC[A/G]AACTACTCATAAGCG | 55819 |
| rs367948644 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028880 | TTTTTAAAGTGCCAA[C/T]CTCAAAATGAAAGAA | 55819 |
| rs367987708 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065212 | ACTTTTCCCCCTGTC[C/T]TTTCATGGAAAATTT | 55819 |
| rs368014052 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063827 | TCCACAATGGAAATT[C/T]TGTGTTTACAAAAGA | 55819 |
| rs368096388 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946293 | GCCATAGCCGCGCGG[A/G]GTCTGTGTGTGGTCA | 55819 |
| rs368096539 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926411 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 55819 |
| rs368156443 | snp | A/G | 4.94548e-05 | 0.00497242 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966987 | CATATCGAATGCTAC[A/G]TTATCAGTACATGGC | 55819 |
| rs368168954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180029702 | GTGCTACCACGCCCA[A/G]CTCATTTTTGTATTT | 55819 |
| rs368178455 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180065455 | GGGAAGCTGTACAAA[G/T]AAGTGGTTAAAGTAC | 55819 |
| rs368251039 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954405 | TTAACCACACAAAGA[A/T]GTTCTGACACATGCT | 55819 |
| rs368310592 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953126 | AAAAAATATGAGAAT[A/T]AATGAGTTCAGCAAT | 55819 |
| rs368342161 | in-del | -/CC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070990 | ATTTACACCCCCCCC[-/CC]AATTTACCACTTAAG | 55819 |
| rs368390228 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068458 | CCCACCAATGCATTC[A/G]ACTTAATGACAAAGA | 55819 |
| rs368396788 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023090 | GGCAAGAGCCAGGTT[C/T]TTCATTTAGGAGTGG | 55819 |
| rs368436414 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058573 | TTATTTTTTATTTTT[-/T]GAGATGGAGTCTTGC | 55819 |
| rs368466411 | in-del | -/CTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946512 | TGTACTAGCGTTCTT[-/CTT]AGTCTTAACAGACCG | 55819 |
| rs368487000 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010044 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 55819 |
| rs368503876 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991097 | AAATTTTTCTCCTTT[C/T]AGCACTTTGAAAATA | 55819 |
| rs368563163 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974340 | CACACTCCGATGGCC[A/G]ACCTTTAAGAGGTCT | 55819 |
| rs368574536 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947924 | TGTATGTGTTTGTGT[A/G]GCTCAGCCCTCAAAT | 55819 |
| rs368589015 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045582 | TATTCCCTTATCTGA[A/C]CCCACCCACATCCTA | 55819 |
| rs368602894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035457 | GCTCCATGTGTGCCT[G/T]AAATGAATGTGTATT | 55819 |
| rs368644442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960735 | AGAGGTGGAGTTTAG[C/T]ATCAATTTTTGGACA | 55819 |
| rs368649898 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035017 | CAACTTTTGGGTTTC[A/G]TTGACTTTCTCTATG | 55819 |
| rs368708175 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068598 | TTGACTATTTGCTCT[C/T]TAAAGGGATAGGACA | 55819 |
| rs368728115 | snp | G/T | 6.59196e-05 | 0.00574068 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966884 | AGATCCCCGAAGTTC[G/T]AAGTGGCTCAAGGCC | 55819 |
| rs368768839 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981749 | CCCTAGGTGTTTACA[C/G]AATGTCTTTAAGCAG | 55819 |
| rs368812114 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036126 | ACATTTTAGACAGTA[C/T]ATTGTAGCAACTCTG | 55819 |
| rs368831211 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053374 | CATTTCAGAGTTTAC[A/C]AAATCCTGGGCAAAC | 55819 |
| rs368847244 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992049 | CTGTAAATACAAATG[A/C]AGCTTCAGTCACTCA | 55819 |
| rs368856216 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984941 | ATAATGCAAATATTC[C/T]AGAATCTGAAAAATT | 55819 |
| rs368857208 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974693 | GTGGGGCAGTACTTG[A/G]AGGGCGATGGCTTTG | 55819 |
| rs368873277 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007988 | AAAACAAATCTTTTA[G/T]TTTTTTTTTTTTTTT | 55819 |
| rs368879412 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033312 | TTCTCTCAGTAATGT[C/T]TGTAGGTTCAATGTG | 55819 |
| rs368912285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179949201 | AACTCCTGACCTCAG[A/G]TGATCTGCCTGCCTT | 55819 |
| rs368935141 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949373 | GGGCTCAAGTAATCT[G/T]CCTGCCTCCTGAGTA | 55819 |
| rs368972253 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966292 | CAACTACACCAAAGA[C/G]TTAAGTGCCAAGAGA | 55819 |
| rs369056648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970259 | ATCTGGTAAAAAGGT[C/T]CTGTTGGGCTTACAT | 55819 |
| rs369058752 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928735 | CTGGGTTCATGCCAT[G/T]CTCCTGCCTCAGCCT | 55819 |
| rs369064191 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940286 | CAGGCTGGGGTGCGA[A/T]CTCGGCTCACTGCAA | 55819 |
| rs369122516 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978941 | ATAAAACAAAACATG[A/C]CAGGAACCTAAGCCA | 55819 |
| rs369128413 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049309 | GATCAGCAGCTACAG[C/T]AAGCATTCTTGACAA | 55819 |
| rs369136295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006056 | GCAGGACATGAAAAA[A/C]AAGGTATCAGAGTAT | 55819 |
| rs369137198 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934097 | TTAGAAACCGGAAGA[C/T]GACTTTGAAGCACGG | 55819 |
| rs369139985 | in-del | -/CA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961244 | TACACAACATGCACG[-/CA]CACACACACTCTCTC | 55819 |
| rs369184853 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944980 | GTATCTGCACCTGTT[C/G]AAAGTTATAACTGGG | 55819 |
| rs369240758 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997552 | CCAGGATGGTCTTGA[A/T]CTCCTGACCTCGTGA | 55819 |
| rs369243733 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034312 | TTTTGTGCCTACATT[C/T]GTAAGGGATATTGGT | 55819 |
| rs369267739 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040448 | CAACCCTCATTTTTG[C/T]TTACCTGGATGAGTC | 55819 |
| rs369302040 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050173 | ATGTAGATACAAAGG[G/T]ATTTATTATAAGGAA | 55819 |
| rs369307012 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066789 | GGTGAGCCGAGATCG[C/T]GCCATTGCACTCCGC | 55819 |
| rs369309707 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958035 | GGCGCCCGCCACTAC[A/G]CCCGGCTAATTTTTT | 55819 |
| rs369328042 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935534 | TGTGTGTGTGTGTGT[A/G]TACATTTTAAATCTA | 55819 |
| rs369365790 | in-del | -/GGGCTCCGGAATCGGAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017802 | GAATTAAGCTCCTTT[-/GGGCTCCGGAATCGGAG]GGTCTAGGTTCAAAT | 55819 |
| rs369386835 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934540 | ATTTCTTTTCTTTCC[-/T]TTTTTTTTTTTTTTT | 55819 |
| rs369414872 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997988 | CTGAGACTACAGGTG[C/T]GCGCCACCACACCCA | 55819 |
| rs369416432 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061545 | AAAAACCACCTCCAG[C/T]CCCTCTCCCAGCGTC | 55819 |
| rs369422875 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030872 | GAGTTAATTCCATTT[A/G]CAGCTGAGAATACCA | 55819 |
| rs369438114 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067804 | GCCCCTGCCTTTGCT[A/G]TTATGAATTCAAACA | 55819 |
| rs369441327 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179948875 | AGCTGCTGGGTAGAA[C/T]CAGGGGCACTTGCTT | 55819 |
| rs369447696 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018575 | TTCAAGGTGAGATTT[C/G]GGTGGGGACACAGAG | 55819 |
| rs369454875 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052666 | AGGAGCCATGCAGCT[C/T]ACACTAACAGGGAAG | 55819 |
| rs369498216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180039600 | TATCAAGATGTGTGG[A/G]GAAGTACCAACGACT | 55819 |
| rs369511186 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066883 | TAAAAAAATTAGCCA[C/G]GTATAATGGCATGCA | 55819 |
| rs369568209 | in-del | -/CT/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995202 | CTCTCTCTCTCTCTC[-/CT/TC]CAGAACCATCAGGAC | 55819 |
| rs369591772 | snp | C/T | 8.2543e-05 | 0.00642376 | intron-variant | RNF130 | GRCh38.p7 | 5:179978153 | CCTGAAAAGGAGGCA[C/T]ACAAAGCACATTAAT | 55819 |
| rs369641294 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932680 | CTGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 55819 |
| rs369663950 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921485 | AAACTGAACTTTTTC[A/G]GAAACTGCCAGGCTG | 55819 |
| rs369738554 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012458 | CACCATCTCCAGGCC[C/T]TCACACCGGGGAAGC | 55819 |
| rs369850205 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963386 | ACTGGTAGAAAGCCA[A/G]TTCTCACCACCTTCA | 55819 |
| rs369859727 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952952 | ATGGATGTCTGTTTG[C/T]ACCATTTCTATTCAA | 55819 |
| rs369870560 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037365 | GGCAAACAGCAGTTG[C/T]GCTCCACCGTAGGCA | 55819 |
| rs369907806 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071205 | ATGCCCTCCAGCAAA[A/C]GAGCTGCCTGAACGC | 55819 |
| rs369961797 | snp | A/G | 6.59e-05 | 0.00573983 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179978238 | GACATCATTCTGCTT[A/G]TAGCTCTCTATGCAG | 55819 |
| rs369966128 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038296 | CTGGGCTCAAGCAAT[C/G]CTCCTACCTTGGCTT | 55819 |
| rs369975739 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993640 | GCCCTTTGTCAGATG[A/G]GTAGATTGCAAAAAT | 55819 |
| rs369975848 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046219 | ACCGGGGCAGGTGCA[G/T]GGCCCGCCAAGCTCA | 55819 |
| rs369979831 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013751 | AAATGGAGTAAAGTG[C/G/T]TGTTTTTATAGCATA | 55819 |
| rs369987131 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025128 | GAGATCCTCACCCAG[A/G]CCTCTAACACCTATA | 55819 |
| rs370003812 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:180060880 | CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 55819 |
| rs370020672 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938730 | TATATTAAACCAGAA[A/G]TATATTATCATTATT | 55819 |
| rs370028378 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040574 | GTTTCCCCTCTGCAG[C/T]AAGGCAATCCACTGT | 55819 |
| rs370085099 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952515 | TGATGCCAGCATTAC[A/C]ATAATACCAAGGTCA | 55819 |
| rs370090657 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959226 | CCTTCAAACACCTGG[A/T]AACAGCTCTCATCTT | 55819 |
| rs370201588 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981743 | CAATTTCCCTAGGTG[-/T]TTACAGAATGTCTTT | 55819 |
| rs370237906 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179930307 | GTGATCTGCCCGCCT[G/T]GGCCTCCCAGAGTGC | 55819 |
| rs370248635 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020787 | TCCTTCACACACAGA[C/G]GCAGAAGGGGGGTGG | 55819 |
| rs370270273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976049 | AAAAGAGGGCCAGAC[A/G]TCAGGCTCATGCCTG | 55819 |
| rs370271435 | in-del | -/GGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063041 | TGGGGGTGGGGAGGA[-/GGA]AGGGGCTGGAGCTAG | 55819 |
| rs370271953 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967315 | CATTAACATAAAGAT[A/G]GCAAACATCCAGTTT | 55819 |
| rs370274142 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986441 | GGTGTAATATTCAAG[A/G]TTCATGATACTGCAC | 55819 |
| rs370276622 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053286 | TGGCCAGGCATATCC[C/T]GGTGAACAGCTGCCC | 55819 |
| rs370290235 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009485 | GATGGCAAACAAGCA[A/C]ATAAAAAATGTCTAA | 55819 |
| rs370302919 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007487 | CTAATATTATGGCTT[C/T]TCTTTTAAAATAGCC | 55819 |
| rs370374930 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | RNF130 | GRCh38.p7 | 5:179951684 | TAAGAGAAGCCTTAA[-/T]AAATTTATGATTGAA | 55819 |
| rs370396795 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973228 | ATTCCCATGGCACAT[C/G]CCTCGCTTCCACAAA | 55819 |
| rs370398538 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047926 | ACCTTCAATACTGAC[A/G]CTCCCGAGTACTCTG | 55819 |
| rs370450977 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946133 | AAGCCCCAAGCTCCT[A/C]GGGTGCAACCCCCTA | 55819 |
| rs370452824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025855 | TACTCATTTTCTTGA[C/T]AGGCATTTAGAATAA | 55819 |
| rs370525495 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067826 | ATTCAAACATTACAT[A/G]ACCCCTTTCACCCAA | 55819 |
| rs370574695 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998784 | AGATGATCTGTCTAA[C/T]GCTAAGAGTGGGGTG | 55819 |
| rs370658766 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945880 | CTGCATGCATTTATA[C/T]CCACTCAACAATAAA | 55819 |
| rs370679897 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:180068190 | CACTCTGGGGCCAAA[C/G]AAAAAGTTAGTGTGC | 55819 |
| rs370717516 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180045324 | AAGCCGCGGACCCTC[A/G]CGGTGTTACAGTTCT | 55819 |
| rs370726913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999934 | CCTTTGTTATTTTTG[C/T]TCTCTCCTATTGTTT | 55819 |
| rs370734364 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932217 | TTGTAATTTTAAGTT[C/T]CATGTGTTTAATCAT | 55819 |
| rs370753341 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951402 | TTGTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT | 55819 |
| rs370769164 | snp | A/G | 0.00095533 | 0.0218347 | intron-variant | RNF130 | GRCh38.p7 | 5:179980080 | CCACCAAACAAAAAC[A/G]AAACTGCTGGATTAC | 55819 |
| rs370787826 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179980416 | CACCCTGTTAGGTCA[A/C]ACAGAAATATAGAAC | 55819 |
| rs370823774 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027350 | ACATTGATGAGCCTG[C/G]AAAGCAAGGAGTTGC | 55819 |
| rs370829922 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003215 | TGACTGACATGGAGG[A/C]ACGAAGAGGGGGGTT | 55819 |
| rs370836586 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019796 | CTGCTTTCAAAAGCC[C/T]TTGATGTATCCCTTC | 55819 |
| rs370848810 | snp | A/G | 8.23676e-05 | 0.00641693 | missense | RNF130 | GRCh38.p7 | 5:179980197 | CTGCATCTCCGAGAC[A/G]ACGCTATGAAAATTG | 55819 |
| rs370873938 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965955 | CCACGAGCCTCAGGG[C/T]GTGACGTGCTAGGCA | 55819 |
| rs370912581 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015840 | AAGAACACTAAATAA[C/G]AACACCAACTAATTT | 55819 |
| rs370932139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180045696 | AGTGCTGATTGGTGC[A/G]TTTACAAACCTTGAG | 55819 |
| rs370935163 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179972505 | GCTCTGGTGCAGGAA[C/T]GGGAGGCATCCCGCT | 55819 |
| rs370935438 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068858 | CCTGTCTGATAACTT[C/T]GTGTGTAATCTGAGC | 55819 |
| rs370937819 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059249 | TCTGCTCATGCTGCC[A/G]TCTCAGCTGAAACAT | 55819 |
| rs370948457 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924422 | ATCACTTGAACCCAG[A/G]AGGCGGAGGTTGCGG | 55819 |
| rs370969099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008809 | GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTGC | 55819 |
| rs370980975 | in-del | -/G | 0.0029935 | 0.0385719 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015469 | AGGGAAAGGAGTAGG[-/G]AAAGGAGTAGGGAAA | 55819 |
| rs370982331 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963637 | TGCCAACATTTCCCT[A/C]AAATGCAACGAAGCA | 55819 |
| rs371013354 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942163 | CACTTAGAACCATCT[A/C]AGTATGAAATAAAGA | 55819 |
| rs371043765 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180047580 | TGAAACCCTGTCTCT[A/G]TTAAAAATACAAAAT | 55819 |
| rs371044032 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062529 | GCACCTACTACACCC[G/T]TTAAGTGGAATATTA | 55819 |
| rs371070754 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971800 | GATTTATAAAAAGAG[A/G]TCTAGAGAACTCAGT | 55819 |
| rs371096198 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180013550 | AGAACGACTGCAGTG[C/T]TAAGAACCATATTAA | 55819 |
| rs371207462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930195 | CCCGAGTAGCTGGGA[C/T]TACAGGCATCTGCCA | 55819 |
| rs371226485 | snp | C/T | 8.23676e-05 | 0.00641693 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013193 | ACGGCTGAAGTTCTT[C/T]GGTGGCATTCGAGTT | 55819 |
| rs371254554 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041589 | TATAACAGGTTCAAA[C/T]GAGAGAGAAGGGCAG | 55819 |
| rs371305213 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180040334 | TCCCAACAAACAAAT[A/G]GCAATACTAATAGGA | 55819 |
| rs371305870 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016973 | GTGTTCTTTAATAGA[C/T]GGTCCATTTTCAGGT | 55819 |
| rs371316305 | snp | C/T | 0.00035314 | 0.0132833 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015350 | GACGGATCCCACAAA[C/T]GACATATGACAATCA | 55819 |
| rs371317047 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995824 | AATTTCTCTTTCCCA[A/G]TGTCTGAAATGTTCT | 55819 |
| rs371318400 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975350 | TTTGGTTGTCACAAC[C/T]GTGTGTGGGTGGGCG | 55819 |
| rs371331237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180037756 | AGATTCTTTTAACTA[C/T]ACCACATAATGCCAA | 55819 |
| rs371346102 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066735 | CCAGCTACTAGGGAG[G/T]CTGAGGCAGGAAGGC | 55819 |
| rs371371677 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955878 | ATCTTAGAGGTGCTT[C/T]AATACTCCCAAAAGG | 55819 |
| rs371398257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997385 | CTGGAGCGCACTGGC[A/G]CAATCTCGGCTCACT | 55819 |
| rs371411209 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | RNF130 | GRCh38.p7 | 5:179966895 | GTTCGAAGTGGCTCA[A/G]GGCCAAGGGAGTTGT | 55819 |
| rs371427028 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974379 | CAGGTGACAGTTCCT[C/T]GGTTTCTAAGACCTG | 55819 |
| rs371471474 | snp | A/G | 0.000597326 | 0.0172715 | intron-variant | RNF130 | GRCh38.p7 | 5:180013031 | AACTCTGGCTGTTAC[A/G]AACCAATCACTGTTG | 55819 |
| rs371539369 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031791 | GACTGCTGGGTCATA[C/T]GGTATTTTTATGTTC | 55819 |
| rs371543771 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955573 | ATAAATGCTTGTGTG[G/T]CATGATTGGTAAATG | 55819 |
| rs371574100 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962405 | CAATGGGCAGTCAAT[C/T]ACATCAACTGCATGA | 55819 |
| rs371588596 | snp | A/G | 5.64398e-05 | 0.00531194 | intron-variant | RNF130 | GRCh38.p7 | 5:179966786 | ACATGCCCTGTGCCT[A/G]AGCGGAGGCCCCCAC | 55819 |
| rs371601003 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180017442 | TTCCAGATTGTGTGA[A/C/T]TAGCCAGTTCCCCAA | 55819 |
| rs371602798 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977553 | AACATAGTGAGAACC[C/T]CATCTTTAAAGAAAA | 55819 |
| rs371738321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180045973 | CCTCAGCCCCTGGGC[A/G]GTGGATGGGACCGAG | 55819 |
| rs371751598 | in-del | -/T/TT/TTT | 0.49928 | 0.018956 | intron-variant | RNF130 | GRCh38.p7 | 5:180007988 | AAACAAATCTTTTAG[-/T/TT/TTT]TTTTTTTTTTTTTTT | 55819 |
| rs371756895 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180053578 | GTTGAAGGTTGCCAG[G/T]AATGATAGGAACAAG | 55819 |
| rs371770048 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932471 | CACCATATTGGTCAG[A/G]CTGGTCTCAAACTCC | 55819 |
| rs371793327 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977353 | GCCAGGTGAGCTCGA[C/T]GGAAGTCTCACTGAA | 55819 |
| rs371941440 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180028967 | GTACAACTGTTATAC[A/G]TTACAGTTTGTTAGC | 55819 |
| rs371960267 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180064524 | TTCTTGGTTTGCCAA[C/G]TTTGGAAATTGTGTG | 55819 |
| rs371975250 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946704 | GACTACAGGCGCCCG[C/T]CACCACGCCCGGCTA | 55819 |
| rs371975570 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035397 | GTCTTTGAAAATATA[C/T]TCAGACTTGATTTAC | 55819 |
| rs372011920 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043240 | TGAGATGGGAGGATC[A/G]CTTGAGCCCAGGAGT | 55819 |
| rs372014910 | snp | C/T | 3.42366e-05 | 0.00413729 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013304 | GACAGCAATAATATC[C/T]CCAGTGCCTGCAATA | 55819 |
| rs372059105 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016542 | CCCACGCACTTCCAC[A/G]TCTGGCCGCCAGTAC | 55819 |
| rs372070750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179991339 | AGTCCTTTTGCAATG[C/T]ATTTGCCTGTTAATC | 55819 |
| rs372073646 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942701 | TAGCTGTTTAAACTG[C/T]AATCATTAGAGTACA | 55819 |
| rs372122286 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962033 | AGCTTCAAATAAATA[C/T]AACTGCCCAGGTCTT | 55819 |
| rs372122855 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982646 | AGTGGTGCAAACACG[C/G]CTCACTGTAGCCTTG | 55819 |
| rs372132342 | snp | C/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072643 | AGGCGTTAGATTCTC[C/G]TAAGAAGTGGGCAAC | 55819 |
| rs372138788 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant | RNF130 | GRCh38.p7 | 5:180027045 | CTTTTGACTTTTACC[A/C/G]GTTCTTACTAGTTCA | 55819 |
| rs372141571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059688 | CAATGAAGGTGAGCC[A/G]TGAAAACAACTGACC | 55819 |
| rs372235034 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040979 | ACACAGACGAGAAAC[A/C]CAGGTGACTGATGTA | 55819 |
| rs372241390 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021051 | CAGTGGCGCAATCTC[G/T]GCCTCGCGGGTTCAA | 55819 |
| rs372262884 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995475 | ATCCTGGCATGAGAC[C/T]TTATAATGCTAACAG | 55819 |
| rs372287941 | snp | A/G | 0.000101197 | 0.00711253 | missense | RNF130 | GRCh38.p7 | 5:180071614 | TAGTACTCCTGGCTC[A/G]CGTTGTCTGCCCGTG | 55819 |
| rs372290425 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976759 | TGTAAGTAAAATAAG[A/G]CCAGTAGCCTCATGG | 55819 |
| rs372296455 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927117 | GTCATCAGCTGATAC[C/G]AAATCTTTGGCAATA | 55819 |
| rs372330343 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005193 | AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA | 55819 |
| rs372346406 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:179938149 | TTTTTGTAGAGATGG[A/G]GTTTTGCCACGTTGC | 55819 |
| rs372360072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922263 | CGTTTGTGAAGTGTT[C/T]TGTTCAAATCTTTAG | 55819 |
| rs372371758 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984093 | TTCATTACTCATATA[C/T]AGAAATAAAATTAAT | 55819 |
| rs372376690 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001012 | TTTCAAATTTTCTAG[A/G]GTGGCTCTCCTGGAC | 55819 |
| rs372387113 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963163 | TGCTGACAGCCTTTT[A/G]CACTCTAAGACTATA | 55819 |
| rs372405228 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974320 | AAACGTACTTCTAAC[A/G]ACTACACACTCCGAT | 55819 |
| rs372440135 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010063 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 55819 |
| rs372501463 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986611 | GCAACAGGTGGCTAT[A/G]AAATTATTACATTAA | 55819 |
| rs372505749 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004533 | AGACTTTCTATAGCA[A/T]ACAGCTTGAGGGGTT | 55819 |
| rs372505991 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933482 | CTATTTATTTATTGT[C/G]GTTTTTGTCCATTGA | 55819 |
| rs372510829 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179968394 | CTGTTGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 55819 |
| rs372513608 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944372 | CATGATGGAAACTTC[A/G]TTGTGTTCCTATAAT | 55819 |
| rs372531896 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179921105 | TTCTATAAAACTGTT[A/T]TTAAGCTTTACTGGG | 55819 |
| rs372660766 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035528 | CAAGTTGGTTAATAG[C/T]GTTGGTCAAGGTTTC | 55819 |
| rs372680501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180068677 | GCAAAGCGAACAGGA[A/G]GGTTTCTAGTTTCAT | 55819 |
| rs372698882 | snp | A/T | 0.00561005 | 0.0526645 | intron-variant | RNF130 | GRCh38.p7 | 5:180050587 | AATTCACCATCACAG[A/T]CCTCCTCACAGCTCA | 55819 |
| rs372721475 | snp | C/T | 0.000100786 | 0.00709809 | intron-variant | RNF130 | GRCh38.p7 | 5:179978319 | AAACAAAAAGTCACA[C/T]GCTGCAAGTATATAA | 55819 |
| rs372766627 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935537 | GTGTGTGTGTGTATA[C/T]ATTTTAAATCTATCT | 55819 |
| rs372840582 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033437 | ATAGAAATACAATGG[C/T]TTTTGGGCAGGCCCA | 55819 |
| rs372874623 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974761 | GTCACGAGATGCCGG[C/T]GAGTGGAGACAGAAC | 55819 |
| rs372878254 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992277 | CTCCCGAGTAGCTGG[G/T]ACTACAGGCACCCGC | 55819 |
| rs372878308 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939150 | TGAACTCGGGAGGCA[A/G]AGGTTGCAGTGAGCT | 55819 |
| rs372884267 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929318 | GTTCTGCTGTCTGTC[A/C]ATCCTTGCATCGATA | 55819 |
| rs372911984 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065527 | GCACTTTGGGAGGCC[A/G]AGACAGGCGGATCAT | 55819 |
| rs372922643 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061553 | CCTCCAGCCCCTCTC[C/T]CAGCGTCTGATGGCT | 55819 |
| rs372933990 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017259 | GTAAGAATACCACAA[G/T]GTGATGGCGTGTCCC | 55819 |
| rs372939047 | in-del | -/GAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957322 | GAAGCTGAGACAGAA[-/GAA]CTGCTTGAACCTGGG | 55819 |
| rs372986085 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002543 | GTGGGGTGCATAGCC[A/G]GGTGGACTCAGCTGG | 55819 |
| rs373006212 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979205 | GTCACCACTCCTCTG[C/T]CATTGAAATGCAAGC | 55819 |
| rs373037471 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939284 | TTAAGACAGAAAAAA[A/G]GTGGTCCTATTATGT | 55819 |
| rs373087083 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985818 | CTTACTAATAAATGT[C/T]CTTTGTGGCACTTTC | 55819 |
| rs373096468 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921731 | GAACCCAGGAGGTGG[A/C]GGTTGCAGTGAGCCA | 55819 |
| rs373166284 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974281 | GGAAACATACGTTCA[C/T]CCACGCGGCAACTCC | 55819 |
| rs373179449 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047158 | TGCTTTCCTACTCCT[A/G]AATTAGATTATAATT | 55819 |
| rs373222200 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044827 | ACGGAAGTAGACTCC[A/G]TCTCAAAAAAAAAAA | 55819 |
| rs373232025 | snp | A/G | 1.65781e-05 | 0.00287902 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015285 | AAAATGTTGTTCAAC[A/G]GGCCATGATCTGTGG | 55819 |
| rs373236829 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180058070 | AGAGTGCTGCAGGTA[A/G]AAAGCTGTCCTTTAC | 55819 |
| rs373251583 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971612 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 55819 |
| rs373266260 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924364 | GCCAGACATGGTGGC[A/G]CATGGCTGTAATCCC | 55819 |
| rs373272267 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179942262 | GTTATGGTAGTTAGA[C/T]GGCTTTAATGAAGAT | 55819 |
| rs373294973 | in-del | -/GTTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982588 | GTTTTGTTTTGTTTT[-/GTTTT]TAAGACAAGGTCTTG | 55819 |
| rs373320071 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034093 | CTAATGTGTTAAATG[-/C]TTTTTTTTTTTTTAA | 55819 |
| rs373356432 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179949317 | ATGCCCAGGCTGGAG[C/T]GCAGTGTTGCAACCA | 55819 |
| rs373393654 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:179992303 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 55819 |
| rs373455849 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026388 | AAAATAAATCCATAA[C/T]TTTCAGACAAGTATG | 55819 |
| rs373524615 | snp | C/T | 0.000115326 | 0.00759274 | missense | RNF130 | GRCh38.p7 | 5:179978222 | AGGGGAGAATTCGGA[C/T]GACATCATTCTGCTT | 55819 |
| rs373536243 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972583 | GTGCAGGAGTGAGAG[A/G]TATCCAGATGAGGGT | 55819 |
| rs373549793 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051486 | TTGTGATCTGCTTGC[C/T]TGGGCCTCCCAAAGT | 55819 |
| rs373586083 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054649 | GTAAGTTTTCAAATT[A/G]AGAAATGTGAATTCT | 55819 |
| rs373624205 | snp | A/G | 0.00028011 | 0.0118312 | intron-variant | RNF130 | GRCh38.p7 | 5:179980102 | CTGGATTACTTTTAC[A/G]GTGCTGAAGTTGTTT | 55819 |
| rs373694953 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179992729 | ATTTTTTATGGTTTA[-/T]TTATTATTATTATAC | 55819 |
| rs373706100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179931607 | AACTATGTCTCTACT[A/G]AAATAGAAAAAATTA | 55819 |
| rs373727024 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000563 | CATAAGTTTTGTAGG[C/T]GTTCTTCATTATTTT | 55819 |
| rs373730157 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974741 | CTGGACTGGGAAATG[C/T]GAGTGTCACGAGATG | 55819 |
| rs373746401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065577 | CATCCTGGCTAACAT[A/G]GTGAAACCCCGTCTC | 55819 |
| rs373793345 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071309 | GGAGCAGGCCGGGCT[A/G]TCCACGACGGAAGCC | 55819 |
| rs373816859 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963646 | TTCCCTCAAATGCAA[C/T]GAAGCAGACGTCAAC | 55819 |
| rs373824991 | snp | C/T | 0.000132807 | 0.00814774 | missense | RNF130 | GRCh38.p7 | 5:180013074 | ACCTGGTTCCTGTCG[C/T]GTGCATTTGTGTACC | 55819 |
| rs373830461 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180019857 | CTGGACACTCAAGCA[C/G]TGGGGAGCCACATGG | 55819 |
| rs373926285 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant | RNF130 | GRCh38.p7 | 5:179967410 | AAACACCTCTTTCAT[-/C]CTACTAACTTCTCTA | 55819 |
| rs373936123 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980445 | ACTATAGGTCTTCAA[C/T]TCTCCAGCAGTAAAA | 55819 |
| rs373940107 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179959016 | AAGTGGAAATCTGCC[A/T]CCCTGTAGATATCGC | 55819 |
| rs373948602 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945898 | ACTCAACAATAAATG[C/T]CCGGAGGGAAAAAGG | 55819 |
| rs374006690 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179930336 | GCTAGGATTACAGGC[A/G]TGAGCCACTGCACCC | 55819 |
| rs374062933 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | RNF130 | GRCh38.p7 | 5:180019277 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55819 |
| rs374096826 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067273 | ATGTCTTCATTCCTA[C/T]TAATTTTTTTAAAGC | 55819 |
| rs374197349 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968293 | GAGCAAGACTGTCTC[A/C]AAACAAACAAACAAA | 55819 |
| rs374213299 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966139 | TCAGCTCACTCACAC[C/T]GTCCTGAGGCACCGC | 55819 |
| rs374244034 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954404 | GTTAACCACACAAAG[A/T]AGTTCTGACACATGC | 55819 |
| rs374248526 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930755 | TTAAAATCAAGAATG[C/G]AGGCTGGGCGTGGTG | 55819 |
| rs374249315 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972121 | GTCTTGTTACTCGTA[C/G]CCTCTGTGTGTGGAG | 55819 |
| rs374258848 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937243 | GTGCTTTGAAAGATG[C/T]TATCAAGAAAACGAA | 55819 |
| rs374281606 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928033 | ACAGTTCCTTCCTTT[-/C]TCACCGCCGCATCAT | 55819 |
| rs374288079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055811 | ACCATTACAACTGGT[A/G]CGTGGCTCATGGCTG | 55819 |
| rs374289911 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060885 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 55819 |
| rs374318734 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040736 | TTCTGAATACCACAC[A/G]GAGCTAAAGCACGTG | 55819 |
| rs374335273 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951533 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 55819 |
| rs374353075 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993726 | CAGAAGCTCTTTAGT[C/T]TAATTAGATCCCATT | 55819 |
| rs374394868 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020794 | CACACAGAGGCAGAA[C/G]GGGGGTGGGCACTGA | 55819 |
| rs374429147 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028029 | TTCTGCTCTGAATTG[A/C]ATTTACTATTACCCT | 55819 |
| rs374436423 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955188 | TGCAGCTCTGGTGGA[C/G]GCTGATCAACCACAG | 55819 |
| rs374438161 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179986263 | TTTATGTGTTTTACA[A/G]TGATATGCTAAGTCA | 55819 |
| rs374448314 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063103 | GAGACTTCTGATGTC[C/T]GTTCTAAGGATGATG | 55819 |
| rs374487020 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941061 | TGTTATTTCCACTTA[C/T]TGGTCATTGGTTTCC | 55819 |
| rs374505311 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998082 | CTTGACCTCGTGATC[C/T]GCCACCTTGGCCTCC | 55819 |
| rs374507333 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924467 | GCCATTGCACTCCAG[C/T]CTGCGCAACAGAGCA | 55819 |
| rs374513877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179978379 | TTTCTGTGGCTACTA[C/T]GGTAAGCAAGTGTTA | 55819 |
| rs374514029 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957765 | GAGAAAGAAAAGGAT[C/G]CACTATCCAGCAATA | 55819 |
| rs374519776 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073016 | CTAAAAGGAAGAATG[G/T]GGCAGTGCAGCCGAA | 55819 |
| rs374542440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180024505 | CTCATCAGAAAAAAA[C/T]GTAAGCCAGAAAACA | 55819 |
| rs374557846 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973987 | CCCTCCCCTTTCCTA[C/T]GTCCCACACATGCCA | 55819 |
| rs374564800 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973001 | CAACTGGTTCTCTGG[C/T]GACAAATTTAGAAAA | 55819 |
| rs374588204 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180058932 | GCACAACAGTGGAAA[C/T]GTACTTACCATGACT | 55819 |
| rs374593709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016096 | AGAGCCGGGCAGAGG[A/G]GCCCGACCCTGCCGA | 55819 |
| rs374670797 | snp | A/G | 6.60338e-05 | 0.00574566 | missense | RNF130 | GRCh38.p7 | 5:179966868 | TCCTGAGGAAGAGGT[A/G]AGATCCCCGAAGTTC | 55819 |
| rs374673219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180049689 | GCCCACAGGTTAAAT[C/T]AGACTGCAAAAGGAG | 55819 |
| rs374686925 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058988 | GTTATTTTACCACAA[C/T]TAAAAAATCTTAAAA | 55819 |
| rs374707880 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053034 | TAATGTACGTCCTTC[A/C]AGGAATCCCAAGTAA | 55819 |
| rs374751246 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062055 | CCCCTCCCCCAGCCT[-/C]TTTTTTTTTTTTTTT | 55819 |
| rs374751753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053194 | AGGATAGGGCATGGA[C/T]AGGGATTGCAACCAC | 55819 |
| rs374776473 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928251 | GTGCATATTTTCAGC[A/G]TCAGCAGACACTGGC | 55819 |
| rs374782236 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:180035635 | ATTGAAATGTCTGTT[C/T]CTCCTTCCCATTCTG | 55819 |
| rs374784824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991903 | GGCATTAGATTCTCA[C/T]GAGGAGCACTCAACC | 55819 |
| rs374788066 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990407 | AATTTTGCTATTGCT[A/G]TCTAGAGGGCGGAGC | 55819 |
| rs374813406 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929747 | AGTGAGACTGTGTCT[A/C]AAAAAAAAAAAATTC | 55819 |
| rs374853829 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | RNF130 | GRCh38.p7 | 5:179963435 | TTTTCCTGGGATCAT[C/T]TGGCACATGCAATCC | 55819 |
| rs374880235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063799 | ATGAGAAAGACCAAC[A/G]GTACATGGTTCATCC | 55819 |
| rs374946938 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046343 | GAGCAGACACCAAGG[C/G]GAGGAGGCACCGAGA | 55819 |
| rs374950257 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001796 | AGGATAGCACAGTGA[C/T]AATTCCACTCTCCAA | 55819 |
| rs374960066 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179952774 | TAGACACAAAGCTTC[C/T]GACAGAATCAAAAAC | 55819 |
| rs375005096 | snp | G/T | 0.000164728 | 0.00907398 | intron-variant | RNF130 | GRCh38.p7 | 5:179980211 | CGACGCTATGAAAAT[G/T]GCAAATAAAAACAGA | 55819 |
| rs375009616 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970618 | CCCCCTTTCAGGACA[C/T]ATTTTAAGCCCCAAG | 55819 |
| rs375019993 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031400 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 55819 |
| rs375023644 | snp | C/G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989470 | TTGAATTGTCATATC[C/G/T]TCCTGCAGAATTGAT | 55819 |
| rs375026014 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007567 | AAGCTAAGCTTTTTA[A/G]GCCACATAAAAATTT | 55819 |
| rs375082226 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052681 | CACACTAACAGGGAA[A/G]AAGCCATCTGTCCAG | 55819 |
| rs375095325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179940306 | GCTCACTGCAACTTC[C/T]GCTTCCCAGGTTCAA | 55819 |
| rs375095908 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034325 | TTCGTAAGGGATATT[A/G]GTATATAGTTTCCAT | 55819 |
| rs375104153 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976620 | GATTTTCCTTTATAT[A/G]TAAACTAGAATGACT | 55819 |
| rs375209390 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040361 | AGGATTATGTTGGAA[A/G]TTACATGGCTTCAGC | 55819 |
| rs375222316 | snp | C/T | 3.62693e-05 | 0.00425833 | intron-variant | RNF130 | GRCh38.p7 | 5:179970542 | ATGTCACAAGTTACA[C/T]ACCAAGAAACTTATT | 55819 |
| rs375248340 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016113 | CCCGACCCTGCCGAT[A/C]GGGCAGGAGGACAGC | 55819 |
| rs375262824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056183 | ATATCATGAAGACTA[C/T]CAGAAATATAGATTT | 55819 |
| rs375347480 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977373 | GTCTCACTGAAGGGC[C/T]TGGAGATGTAGTCTA | 55819 |
| rs375375606 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180067532 | GATCAAGTGGTTTTT[A/T]AAAAAATTCAAATAT | 55819 |
| rs375380397 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003603 | ATTTCCCATCACTTT[A/G]CGACAGGTAAACCTG | 55819 |
| rs375387603 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021877 | TTCCCAATAACGTCC[C/T]TTACAGCAGCCCAGG | 55819 |
| rs375404152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179932604 | TCTGTTTGGGAGGCC[A/G]AGATGGATGGATCAC | 55819 |
| rs375420826 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039126 | ACCCCAGTGATCTCC[A/G]GATAGTGAAAAATCA | 55819 |
| rs375433067 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056041 | GTGAGCTGAGATGGT[C/G]TCACCGTACTCTGGC | 55819 |
| rs375434460 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967066 | CACAACCTTTCATAA[A/G]ATTCTAAAAAAGATT | 55819 |
| rs375451082 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179968071 | GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG | 55819 |
| rs375531759 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003890 | TTGAATGCTTAGTAA[C/T]ATATAATAATAAAAT | 55819 |
| rs375555027 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051238 | TTTTGTATAGATATT[-/A]TATTTATTTATTTAT | 55819 |
| rs375602231 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035434 | CCATATGGTCTATCC[A/G]AGAGAATGCTCCATG | 55819 |
| rs375620661 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068591 | AAAAAAATTGACTAT[C/T]TGCTCTTTAAAGGGA | 55819 |
| rs375637597 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036701 | CACTTCGTCTTAACC[A/G]GAAGTGCTACCCCTA | 55819 |
| rs375747978 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066781 | GAGGTTGCGGTGAGC[C/T]GAGATCGCGCCATTG | 55819 |
| rs375749552 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943760 | TAACTTAGATTGCAG[C/T]TATGATTAAACCGCA | 55819 |
| rs375842218 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066411 | TCCCAGTCTCAGGTA[C/T]GTCTTTATCAGCAGC | 55819 |
| rs375842697 | snp | A/G | 3.29484e-05 | 0.00405871 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966909 | AAGGCCAAGGGAGTT[A/G]TCGCCGGCGAGGTCG | 55819 |
| rs375848179 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944330 | ATAAATTAAATAACT[A/G]AAGGATCTGACAAGT | 55819 |
| rs375855730 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028563 | TCCAGACCTGGGTCA[C/G]AACCCCTTTCGTAAT | 55819 |
| rs375866583 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025759 | CTTCAATTCCAAGCT[C/T]CATCTTTTCTGAGGT | 55819 |
| rs375893728 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | RNF130 | GRCh38.p7 | 5:179978230 | ATTCGGACGACATCA[C/T]TCTGCTTATAGCTCT | 55819 |
| rs375908371 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984883 | GCTCACTAGAGCATT[C/T]TGCATTTCAGAATTT | 55819 |
| rs375916455 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055459 | GTGTGTGTGCGTGTG[C/T]GTGTGTGTGTGCGCG | 55819 |
| rs375930137 | in-del | -/ACTG | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016560 | TGGCCGCCAGTACTA[-/ACTG]TCAGAGATGGCAATC | 55819 |
| rs375941374 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985505 | GAAGCCTTCAGTATT[C/G]AATTCATGGGGTTCT | 55819 |
| rs375942701 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965690 | GCTATTAAACGAATC[A/G]AGAGATGGTGAGAAA | 55819 |
| rs375946875 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939983 | GCATCAGACAGCAGC[A/G]CCTCATATGCCTCCA | 55819 |
| rs375968572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002918 | GGTAACTCAGATCTG[A/G]GTTGTTATTATTATT | 55819 |
| rs376071865 | in-del | -/GTAGGGAAAAGA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015778 | GGAGTAGGGAAAGGA[-/GTAGGGAAAAGA]AAGCTGAACAGGTAG | 55819 |
| rs376078682 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058092 | GTCCTTTACACATAA[A/G]TTAAGGAACAGGTAT | 55819 |
| rs376079080 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011959 | GCACAGGGAGAGCCT[A/G]GCACAGAAAGCTTCA | 55819 |
| rs376101031 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974859 | CGGGGAGGAGCGGCA[C/T]GGACCGCAGCAGACG | 55819 |
| rs376224239 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959072 | CATCACTCTGTATGC[A/G]CTGGTTAGTCAACAT | 55819 |
| rs376231335 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179946373 | ACCCACGGTGAGAAA[A/C]CCCGTTTCAAAATGC | 55819 |
| rs376235759 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019894 | GGGTAACTGAGTCAC[A/G]GAACGGTGAACACTC | 55819 |
| rs376238604 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008177 | AGGACCAGAGCAGCC[C/T]ACCACCCGACCCCAG | 55819 |
| rs376241900 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999784 | ATATAATTGTGTCAC[A/G]GTTTTTAAAAATTTC | 55819 |
| rs376248960 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964047 | CTCCCAGCCGTCTGC[A/G]AGCCGGCCTCCCATG | 55819 |
| rs376266850 | in-del | -/ATTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989799 | TAAATTCTTTGTTTT[-/ATTTT]TTCTTCTGTCTTTGT | 55819 |
| rs376278912 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956291 | TCCCCAAATCAAGCT[A/G]TTAGCGTTGATCTTT | 55819 |
| rs376361582 | snp | A/G | 1.86235e-05 | 0.00305146 | intron-variant | RNF130 | GRCh38.p7 | 5:180013332 | ATATAAAATAAATAT[A/G]TAACTCAAGTGACAT | 55819 |
| rs376424069 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061588 | GCCATCCTTTGCACC[C/T]GCCGGTTTGTGGCAG | 55819 |
| rs376457928 | in-del | -/ATTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986900 | ATTCTTATGTATTTT[-/ATTTT]TATGTGACTATTGCA | 55819 |
| rs376481497 | snp | A/G | 0.000235782 | 0.0108552 | intron-variant | RNF130 | GRCh38.p7 | 5:180040435 | AAAACAAAATCAACA[A/G]CCCTCATTTTTGTTT | 55819 |
| rs376575870 | in-del | -/AAAGGAGTAGGG | 6.53744e-05 | 0.0057169 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015446 | AAGACTCAAGCTGGA[-/AAAGGAGTAGGG]AAAGGAGTAGGGAAA | 55819 |
| rs376705447 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005832 | AAGCTCATTCTTGAA[C/T]TCATTGAAATATTTA | 55819 |
| rs376708207 | snp | C/T | 0.000437904 | 0.0147905 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955569 | AAAAATAAATGCTTG[C/T]GTGGCATGATTGGTA | 55819 |
| rs376740630 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962802 | CCTCTGCCTACATTC[C/T]CAGTCCTGAGCGTGC | 55819 |
| rs376740742 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982920 | TTTCCCTATTGTAAT[G/T]ATGTTGACCATCTTT | 55819 |
| rs376767367 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179930758 | AAATCAAGAATGGAG[C/G]CTGGGCGTGGTGGCT | 55819 |
| rs376794188 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924385 | CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC | 55819 |
| rs376805328 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179963279 | TGCTCTTGTTGAATA[A/G]GGTGAATTCCCAATC | 55819 |
| rs376807026 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070991 | TTACACCCCCCCCCC[-/C]AATTTACCACTTAAG | 55819 |
| rs376827881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005482 | GATTATAGAATAAAG[C/T]CTAACTTTCTTATGT | 55819 |
| rs376891536 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957490 | TCCCACTGCCTTTAA[C/T]ACTCATGTTGCAACT | 55819 |
| rs376899612 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998593 | CAAGCAAAACTGTGC[A/C]TAGCTGATATCAAAT | 55819 |
| rs376909280 | in-del | -/AA | 0.254105 | 0.249966 | intron-variant | RNF130 | GRCh38.p7 | 5:180038391 | GTCTCGGGGAGGGGG[-/AA]AAAAAAAAAGCCTGT | 55819 |
| rs376910697 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067365 | TGTTACATATGCCAC[A/G]TCTTCATCAAAATCA | 55819 |
| rs376911841 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032573 | GATAACAATTGTTTC[A/G]GCACTGGTTGTTGAA | 55819 |
| rs376956264 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179990204 | TTATTTATTGGATAC[A/G]AAGTAAAAGGGGCAG | 55819 |
| rs376991218 | in-del | -/GTTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982592 | GTTTTGTTTTGTTTT[-/GTTTT]TAAGACAAGGTCTTG | 55819 |
| rs377054454 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938965 | GGGCACAGCAGCTCA[A/C]GCCTATAATGCCCAA | 55819 |
| rs377085544 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064681 | ATCTCTTGAATCCCC[A/C]TCCTGTGAGATGAAT | 55819 |
| rs377104165 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933613 | TGCACTCTTGACTTC[C/T]CGGGCTCAGGTGATT | 55819 |
| rs377111527 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997955 | CAAGCAATTCTCCTG[A/C/T]CTCAGCCTCCCGAGT | 55819 |
| rs377113242 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048276 | CATGGAAGGGGCACG[A/G]AAGGGAGTCTGTAGT | 55819 |
| rs377118290 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004901 | CTTGTAGTCTGCACC[C/T]TCCTTCATTCATTCA | 55819 |
| rs377120691 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977929 | AGAACAAGAATTCTC[A/G]ACCTCAACACTCCTA | 55819 |
| rs377129611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942815 | CTCTGCGAATTTGCT[C/G]CTATGGGTGACATAT | 55819 |
| rs377141891 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046809 | GGCACCCTTAGGTTA[C/G]ATCCATCTTGGCATT | 55819 |
| rs377144297 | snp | G/T | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015013 | ATACAACAGTAAAAG[G/T]AGTTTTATGGAAAAT | 55819 |
| rs377231994 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998859 | AGATCTAGTATTTTT[-/TA]TATATATATATATAT | 55819 |
| rs377232541 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958152 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG | 55819 |
| rs377234937 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057996 | CAGGTAGTTAGTGTC[A/G]GAATTGAATTAAACT | 55819 |
| rs377246767 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969923 | TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC | 55819 |
| rs377272705 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946987 | GCAAATAAAGTACTC[-/TC]CTTACAGGATCTCAA | 55819 |
| rs377285475 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037732 | GTGAAATTAATGATC[A/G]CAGTGTGCAGATTCT | 55819 |
| rs377293434 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:180060858 | GCGGATCACGAGGTC[A/G]GGCGATCGAGACCAT | 55819 |
| rs377299996 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948286 | GTGATCAGGAGCCCC[-/T]GGCAACAGTTAACAG | 55819 |
| rs377316240 | snp | A/C/T | 3.32701e-05 | 0.00407847 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015337 | ATAAAGTAACTGAGA[A/C/T]GGATCCCACAAACGA | 55819 |
| rs377350704 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052377 | TGAAACACAAAGGAC[A/G]AAAATTCCTGTTGGA | 55819 |
| rs377356648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180033822 | CTATCTGATTTTCTA[C/T]ATACACAACCTATGA | 55819 |
| rs377405214 | snp | C/T | 0.000913723 | 0.0213548 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015411 | AAACGGTTTTAGAAA[C/T]CAGTTGAGGCTCCCT | 55819 |
| rs377405267 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951889 | ACAACAATATCAAAA[C/T]TTACAAATGAGTGAA | 55819 |
| rs377497317 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179972636 | ACTGTTGGTGGGGAC[C/T]TGGTAAAGCCGCAGC | 55819 |
| rs377508544 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939285 | TAAGACAGAAAAAAA[G/T]TGGTCCTATTATGTG | 55819 |
| rs377515986 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949365 | GAACTCTTGGGCTCA[A/T]GTAATCTTCCTGCCT | 55819 |
| rs377521560 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056063 | TACTCTGGCCTGGGC[A/G]ACAGAGCGAAACTGG | 55819 |
| rs377527852 | snp | C/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072266 | GGGCAGCCGGGTCAG[C/T]CGCTGGTGCTGGTTG | 55819 |
| rs377659214 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043713 | CCCGCCCACTGAGAA[A/C]AGATTCTATGAACAA | 55819 |
| rs377713576 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180035843 | CCAGCATGTCTGTCT[C/G]GCTCGGCTCTTTTAT | 55819 |
| rs377717687 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179945901 | CAACAATAAATGCCC[A/G]GAGGGAAAAAGGCGG | 55819 |
| rs377719763 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998093 | GATCCGCCACCTTGG[C/T]CTCCCAAAGTGCTGC | 55819 |
| rs377720839 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925653 | CTTGCCTCAGCCTTC[C/T]CAGAAACTGGGACTA | 55819 |
| rs377721918 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957830 | GGAATTGTTACAAGA[C/T]GGGCTGTGTGAGCAA | 55819 |
| rs377733396 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997472 | GGACTACAGACTCCC[-/C]ACCACCACACCCGGC | 55819 |
| rs377747673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951171 | ACATTCTTCAACCCC[A/G]TATGCACCTAACAAC | 55819 |
| rs377749104 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929582 | GCAAAATCCCATCTC[G/T]ACAAAAAATACAAAA | 55819 |
| rs386695675 | in-del | AT/GAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945925 | AAGGCGGGGGCAGGG[AT/GAC]ATTTAAATGGGGGCG | 55819 |
| rs386695677 | in-del | AGGAATCACAAAACAA/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977426 | GTTTTTGAAACCCAC[AGGAATCACAAAACAA/T]TGCCAAGCACAGTGA | 55819 |
| rs386695678 | multinucleotide-polymorphism | CA/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003266 | CTTCTGGCTCGGTGA[CA/TG]AGCCGTGTGAGAGCG | 55819 |
| rs386695679 | multinucleotide-polymorphism | AG/CC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057518 | GTACCACTGCGCTCC[AG/CC]CCTGGGTGACAGAGC | 55819 |
| rs397690600 | in-del | -/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179938444 | TTAATGAGTAGGGGG[-/G]TTTCTTTTTGGGGTG | 55819 |
| rs397701505 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946571 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 55819 |
| rs397710416 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034105 | TGCTTTTTTTTTTTT[-/T]AAATCATGATGGGTA | 55819 |
| rs397727529 | in-del | -/TTCAT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180034596 | TAGGAATTTGTTCAT[-/TTCAT]CTAAGGTGTCTAATT | 55819 |
| rs397731295 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938443 | CTTAATGAGTAGGGG[-/G]GTTTCTTTTTGGGGT | 55819 |
| rs397754353 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061093 | AAAAAAAAAAAAAAA[-/A]GCTATGTTCATGCAT | 55819 |
| rs397775344 | in-del | -/GC | 0 | 0 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072932 | AACGCGCGCGCGCGC[-/GC]ACACACACACGACTC | 55819 |
| rs397784408 | in-del | -/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179951401 | TTGTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 55819 |
| rs397784550 | in-del | -/CT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179976002 | GCTTTCCAGACCTGA[-/CT]CTGCATCAGAGTCAG | 55819 |
| rs397789463 | in-del | -/ACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005449 | ACAACAACAACAACA[-/ACA]CCAACAGAAACCATA | 55819 |
| rs397799918 | in-del | -/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179945924 | AAGGCGGGGGCAGGG[-/G]ATATTTAAATGGGGG | 55819 |
| rs397807929 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935789 | TTTTACTTTTTTTTT[-/T]AGTTGTTACCCTGGA | 55819 |
| rs397884739 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931033 | CCAAACCTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 55819 |
| rs397932692 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008008 | TTTTTTTTTTTTTTT[-/T]AACAGGTATATTACA | 55819 |
| rs397958544 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944769 | TCAAAAAAAAAAAAA[-/A]GTTCACATGGAGTAG | 55819 |
| rs397968192 | in-del | -/A/G/GC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926552 | ACTCGGGAGGCTGAG[-/A/G/GC]CAGGGGAATTGCTTG | 55819 |
| rs398000097 | in-del | -/TGTGTGTGTGTGTGTGTGTGTG | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179933422 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTGTGTGTGTG]AGTGTGTGGTAAAAA | 55819 |
| rs398000098 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179960858 | GTGAAAAAAAAAAAA[-/A]TCTTATTTTGGTTGT | 55819 |
| rs398000100 | in-del | -/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179985175 | TTTTTTTTTTTTTTT[-/T]GCCATATCCACAATC | 55819 |
| rs398000101 | in-del | -/ATTT | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179988614 | TTTCCATTTTCATTT[-/ATTT]CAAGAACTTAAGAAA | 55819 |
| rs398000102 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180006306 | GGAAGAAAAAAAAAA[-/A]CCTTTTGAACCCACC | 55819 |
| rs398000103 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180033708 | CTTTAAAAAAAAAAA[-/A]GAGAGAGAGAGAGAA | 55819 |
| rs398000104 | in-del | -/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180053842 | TTTTTTTTTTTTTTT[-/T]AATTTGAGACAGAGT | 55819 |
| rs398000105 | in-del | -/A | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180056266 | GGGAAAAAAAAAAAA[-/A]CCCTAATAGTGTATG | 55819 |
| rs398065459 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011777 | CTCTTAAAAAAAAAA[-/AA]GTTTTTTAAATTAAA | 55819 |
| rs398084692 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939283 | TTTAAGACAGAAAAA[-/A]AGTGGTCCTATTATG | 55819 |
| rs398093924 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070991 | TTTACACCCCCCCCC[-/C]AATTTACCACTTAAG | 55819 |
| rs527240833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973329 | CCTGAACACGGCACC[C/T]TTTTCTCCTCATCAC | 55819 |
| rs527261377 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180021857 | CCATCCAAGCTTCTG[C/T]GACTTTCCCAATAAC | 55819 |
| rs527261877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180064064 | TGCCAGAGAAAATGG[A/G]AACACTATGAGCTAG | 55819 |
| rs527268240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933969 | TGCACCTCCAAGTTG[A/G]GGCTGATTATGGCAC | 55819 |
| rs527270895 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072145 | TGTCCGCCGCCGCCC[C/T]GCCCCCCCGCTGGTC | 55819 |
| rs527306168 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961027 | TTTGAGAAAAAGACA[G/T]TGGGTAAGAGTACTA | 55819 |
| rs527309433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926948 | CTTCGTGTGTGGGGG[A/C]CCCCTCGCCCCACTC | 55819 |
| rs527343270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007027 | TCTCAATTGTGAGCA[C/T]TTTACTATGCTTAGA | 55819 |
| rs527344182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179920638 | TCTTCGGATCCCCAA[A/G]AGACTAACCACTGGA | 55819 |
| rs527356096 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984268 | ATGGATGTCTTTTAC[A/G]TCTTTTCCTTTTTAC | 55819 |
| rs527380415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973601 | ACACGGGCAGAGCGG[C/T]CCCGCCACCTGGCCA | 55819 |
| rs527388554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058805 | GACCTCAAGTGATCT[A/G]CCCACCTCAGCCTCC | 55819 |
| rs527397915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005360 | CTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC | 55819 |
| rs527400203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051938 | AGAGCTTGGTCCTCA[C/T]ACAAAGTTGGTGTCA | 55819 |
| rs527405432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007479 | TTCCTTTGCTAATAT[C/T]ATGGCTTCTCTTTTA | 55819 |
| rs527430177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179961519 | TACTGAGCACTCTCA[C/T]TTTAATCTGATGCAT | 55819 |
| rs527441007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179967948 | GATAACCTGCAATAC[A/G]TTTTAGGAGGATTTT | 55819 |
| rs527442468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962014 | TTTATGAATGACTAC[A/G]AGGAGCTTCAAATAA | 55819 |
| rs527474723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052758 | AGAATACAAGGGAAA[C/T]CATAAAATCAGTCCC | 55819 |
| rs527505724 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955269 | ACTGACCATCCTAAG[C/T]GGCATCACCAGCAGG | 55819 |
| rs527516944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000564 | ATAAGTTTTGTAGGC[A/G]TTCTTCATTATTTTT | 55819 |
| rs527524527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053174 | AGATCTCAAAACTGG[C/T]AGACAGGATAGGGCA | 55819 |
| rs527548741 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947848 | CACAATATGCTATTA[C/T]ATATTATACATACAG | 55819 |
| rs527578129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001121 | TACAGTCTCTGTGCA[C/G]TTTCAGCTGAATTCA | 55819 |
| rs527583550 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938396 | ATTGGTAGTTGTCAG[C/G]GGCCGGGGGGATTGC | 55819 |
| rs527598486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993940 | GTTTCAGCTTTCTAC[A/G]TATGGCTAGCCAGTT | 55819 |
| rs527619393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955996 | CATGTTCTGAATGCT[A/G]AGGGTGCTGAAATCT | 55819 |
| rs527619413 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963259 | GGATCTTTTCTCAAA[C/T]GGGCTGCTCTTGTTG | 55819 |
| rs527620381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179948398 | CTCTTGGCCTGGTGC[A/G]TTGGCTCATGCCTGT | 55819 |
| rs527621222 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934955 | TGAGACAAATGCTTC[A/G]AACTTTTCGCTAGGC | 55819 |
| rs527653373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986627 | AAATTATTACATTAA[C/T]ACAGTACGTACTACT | 55819 |
| rs527675053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030832 | TCGTTTAGCATAATG[C/T]TTTTGAGGTTTATCC | 55819 |
| rs527685577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949166 | GATGGGGTTTCGCCA[A/T]GTTGGCCAGGCTGAT | 55819 |
| rs527689002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031443 | AGTGAACCAAGATCA[C/T]ACCACTGCACTCCAG | 55819 |
| rs527695959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179930347 | AGGCATGAGCCACTG[C/T]ACCCGGCCAAAAATT | 55819 |
| rs527715014 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020440 | TCAGCACCCACAGAC[A/G]CACAGCAAAGACCAA | 55819 |
| rs527755335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180023709 | GGGTCCATAATGATA[C/T]AAATAAATGACTGAA | 55819 |
| rs527779143 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957399 | CCTGGGTGAGAGAGC[A/G]AGACCCTGTCTCAAA | 55819 |
| rs527827730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974087 | GCTCTGCAGCCTCTT[A/G]GTGCCATGTAAGAAC | 55819 |
| rs527830570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073110 | CCAGGGTTGAGTCTC[C/T]TGTCTCCTACTGCGG | 55819 |
| rs527865284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180066448 | ACAGACTAATATACC[C/T]TCCCAATATGACTAA | 55819 |
| rs527869859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936847 | GGGTTCCAAGACCAC[C/T]CAGTGGGGGAAAGAA | 55819 |
| rs527869995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179928818 | TATTTTTAGTAGAGA[C/T]GGGGTTTCAACCGTG | 55819 |
| rs527897111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968862 | CTGCTGAACGGTCTA[C/T]GATGCACAGGACAGC | 55819 |
| rs527941697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922667 | TCTAGGCCGGGCACA[A/G]TGGCTCATGCCTGTA | 55819 |
| rs527958414 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030005 | GGTGTGTACCACCAC[A/G]CCCGGCTAATTTTTG | 55819 |
| rs528014336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180002006 | CAAGGCACCAACTCC[C/T]CAAAGGATAATGTGC | 55819 |
| rs528016179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010018 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACAAGG | 55819 |
| rs528059363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179981540 | CAGTACTTTACTTCT[A/G]TTTTTCATCTGTTTC | 55819 |
| rs528071458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033808 | GTTTTTAATAAATTC[C/T]ATCTGATTTTCTACA | 55819 |
| rs528085797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034387 | AAAAACCAGCTCCAC[A/G]GAATAAGTTGAGAAA | 55819 |
| rs528086047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952163 | AGATTGTGCCACTGC[A/G]CTCCAGCCTGGGTGA | 55819 |
| rs528087702 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921284 | GCCCTTCTTTCTACC[C/T]TACTCCTATTGCCAG | 55819 |
| rs528091772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939243 | AATAAATAAATAAAA[A/G]TGCATACAGAGATTT | 55819 |
| rs528128797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939849 | CCACCAAAAATTCCC[C/T]GAAGACATCATCTGA | 55819 |
| rs528149491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027112 | TGCTTCTGCCCTATG[A/C]TGAAGGGAGGGCAAA | 55819 |
| rs528171138 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946627 | GGTGTGATCTTGGCT[C/T]ACTGCAAGCTCCGCC | 55819 |
| rs528201885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983074 | TGTTTTGTATTATTG[A/G]CTTTTGAGAGAACAT | 55819 |
| rs528244121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970957 | ATGTCATTTAAAACA[C/T]CATTTTTAAAAACTT | 55819 |
| rs528254054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179940383 | CCGGCACCACACCCA[A/G]CTAATTTTTATATTT | 55819 |
| rs528258785 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179976206 | CTCCGAATGAAACTG[C/G]AAAAGTCAACACTGA | 55819 |
| rs528260558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019579 | CTCAAATGTTCATCC[A/G]CAACTTTCAGTTCTT | 55819 |
| rs528305522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925075 | ATCCGGGCTTCCTGG[A/C]CTACAACTGCTAGAA | 55819 |
| rs528339764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011405 | TGTTTTTATAAAATA[C/T]ATAACAAAGTATTTA | 55819 |
| rs528352101 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180012412 | ATTCTGTCCACAGCA[C/G]ATCAATCAAACTCAG | 55819 |
| rs528353137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965289 | GCACAGTGCCTGGCA[C/T]ACAGTGGGTGCCAGC | 55819 |
| rs528353596 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179925584 | CAAGCTGGAGTGTGC[A/C]GTGGTGCGATCCTAG | 55819 |
| rs528366292 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963065 | ACAGGCACGGCCGCC[A/G]GGGCTTCCCCAGAAG | 55819 |
| rs528371747 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:179971536 | CACCACGCCCAGCCA[A/T]TTTTTTGTATTTTTA | 55819 |
| rs528381198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057330 | GAGGCGGGAGGATCA[C/T]CCGAGGTCAGGAGTT | 55819 |
| rs528412392 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180043666 | GTTATCAAACATACT[A/G]CAGGAGGACTTTAAA | 55819 |
| rs528413427 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179951397 | GTTTTTGTTTTTTTT[-/G]TTTTGAGATGGAGTC | 55819 |
| rs528413987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005003 | GTGCCCAGATCACTC[C/T]TCTCCTCTCTACATA | 55819 |
| rs528429962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960066 | AAAATAATAAAAATA[C/T]TTATTTTTCTTATTT | 55819 |
| rs528433171 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179966461 | AGCATACAACACACC[A/G]GCAATACTGCTGGGG | 55819 |
| rs528469327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180050064 | ACAGAAATGTATTCT[C/T]CCACAGTTCTGAAGG | 55819 |
| rs528490516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960526 | CCCTTGTGGGGATCC[C/T]CCTTGTGTAGTTAGC | 55819 |
| rs528499946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953148 | TTCAGCAATGTTGTA[A/G]GATAAAAGATCAATG | 55819 |
| rs528509571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998083 | TTGACCTCGTGATCC[A/G]CCACCTTGGCCTCCC | 55819 |
| rs528516544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050911 | TGGGCTCAAGTAATC[C/T]TCCCACCTCAGCATC | 55819 |
| rs528529267 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180005527 | ATAGTCTAGTGACAA[C/T]TTATTCATCTAATAT | 55819 |
| rs528573053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990880 | AATAAAGAGTAATTG[C/T]TACAAACTAATGATT | 55819 |
| rs528575731 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036664 | ATAGTTGCTTTTTTG[A/G]AAGAGGATTTGCTGA | 55819 |
| rs528622808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953915 | TACAACAAAAAACAG[G/T]CCAATTTAAAAATGG | 55819 |
| rs528629064 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059346 | CCGATGCTTTCCCAA[A/G]ACTATGATTAAATAA | 55819 |
| rs528640141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034542 | AGCTACTCAGATATG[A/C]TATTTTTTCTTGAGT | 55819 |
| rs528688399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947502 | GGCAAATAGAATGGG[A/G]TTTGGAACACAGACC | 55819 |
| rs528704245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036573 | TTTTTCAAAGCATAA[A/G]TGTGTCTCAGATTAT | 55819 |
| rs528705360 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968969 | GATCTCTGGAGACAA[A/C]GGACAAATGGGGCAT | 55819 |
| rs528706219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941186 | TGGTCATTTGGTCTT[A/C]TCTCCTGGCTTGCCT | 55819 |
| rs528740087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985072 | TCAAGTCATCTCCTA[C/T]TAATTTAATTACTCT | 55819 |
| rs528742289 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990852 | TGTAGAGTAAGGATT[A/C]CTATAATATTGGAAT | 55819 |
| rs528749538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021294 | CGCCTGGCCAAAATC[G/T]AAATTTCTAAACATC | 55819 |
| rs528765355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029590 | AAAAATAAAAGCAAT[A/G]TTATATTGCAGAATT | 55819 |
| rs528767347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941967 | TCTCATTATGTCTGT[C/T]ATCCTATTTGCTGTT | 55819 |
| rs528798101 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014064 | CCAGGCTTCAACATT[A/C]TGGACCAGTTTGGCA | 55819 |
| rs528801344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179977760 | GGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACC | 55819 |
| rs528825197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179972568 | CTGATCAGGGCTCTG[A/G]TGCAGGAGTGAGAGG | 55819 |
| rs528870943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059890 | CTGTCAGTGAATACA[A/T]CAGGTTACAGAGCAA | 55819 |
| rs528871786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053355 | ATGGAAGAAAGCAAC[A/G]TATCATTTCAGAGTT | 55819 |
| rs528874261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180008703 | CAGCCTGGGCAACAC[A/G]GTGAAACCTCATCTC | 55819 |
| rs528875924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043043 | TGCTTTCTGGCCAGG[C/T]GTGGTGGCACACACC | 55819 |
| rs528876837 | in-del | -/GCA | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179945817 | TCCTGGGCAGTGCAT[-/GCA]GCACGCTTCCAGATG | 55819 |
| rs528878139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963260 | GATCTTTTCTCAAAC[A/G]GGCTGCTCTTGTTGA | 55819 |
| rs528895265 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943938 | GGTCTTTACAAAGGT[C/T]CCATGTAACTAACCA | 55819 |
| rs528903692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956142 | TGTTTCTGTCCTTGC[A/G]TCAGGTGTAAAAACA | 55819 |
| rs528908915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054196 | TTATATCTTATGCAT[G/T]CATGCTGGTTTCTTC | 55819 |
| rs528918846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046102 | CATCTGAGGCCCCAC[A/G]AGAATCTGTGCGCGG | 55819 |
| rs528935403 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941441 | AGTTCCAGGCTGTAG[A/C]CCTTTGGGGATCCCA | 55819 |
| rs528938640 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994026 | GCTTTGTCAAAGATC[C/T]GATAGTTGTAGATGT | 55819 |
| rs529097949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039795 | CTAACAGAACATCAA[C/G]AAAACTAGGGTGTGA | 55819 |
| rs529137599 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073331 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGTTCGA | 55819 |
| rs529147377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179988359 | ACCAAATTTCATTGT[A/G]TTGATCCTTTGTATT | 55819 |
| rs529160544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024528 | AGAAAACAACAAACA[A/C]CACCTTTGAAGTGCT | 55819 |
| rs529172324 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944897 | CAGGCCCTGTTTCCA[G/T]ATAAGGCACATATAT | 55819 |
| rs529191322 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061469 | TAGTCTCATTGTCTC[A/G]CAGTTCTGGGGCCCC | 55819 |
| rs529285952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180067387 | TCAAAATCACTGGCA[C/T]GGCAATAGAAGACCT | 55819 |
| rs529298330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938026 | GTGCAGTGGCATGAT[A/C]ACAGCTCCACAACCC | 55819 |
| rs529302714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930119 | CTAGAGTGCAATGGC[A/G]TGATCTTGGCTCACT | 55819 |
| rs529307515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010076 | CACGGTGAAACCCCA[A/T]CTCTACTAAAAATAC | 55819 |
| rs529329323 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180057320 | TTGGGAGGCCGAGGC[A/G]GGAGGATCACCCGAG | 55819 |
| rs529351235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969552 | TCATCCCATACTCAT[C/T]GACCAACAGAAGCAC | 55819 |
| rs529367943 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180010601 | CTGACCTCAAGTGAT[A/C]CACCTGCCTTGGCTT | 55819 |
| rs529415675 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938107 | GACTACAGGTACGCG[A/G]CACCACGTCTGGCTA | 55819 |
| rs529456787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055885 | GGTCAGGAGTTCAAG[A/T]CCACCCTGGCCAACA | 55819 |
| rs529472027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964550 | AGAACTCTTTACACG[C/T]GGACTGCCAAATGTT | 55819 |
| rs529496523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003509 | GTCAATACCTTCACT[A/G]TAATTTTTCTTTGGA | 55819 |
| rs529507426 | in-del | -/TATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987714 | CGCCTTTTCTGTGTC[-/TATT]GAGAATCTGGTATTT | 55819 |
| rs529535485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958399 | TCTTACAGTAGGAAG[A/G]TGGTTTTTAGAAAGT | 55819 |
| rs529556217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996470 | TAAGTCATATATGGC[C/T]TTTATTGTGTTGAAG | 55819 |
| rs529577260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180041653 | TCTGCAGACTGCTGG[C/T]GCACAGTGGCAGAGG | 55819 |
| rs529596037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951522 | CCGAGTAGCTGGGAC[C/T]ACAGGCGCCCGCCAC | 55819 |
| rs529642775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021171 | CGGGGATTCACCATG[C/T]TGGCCAAAATGGTCT | 55819 |
| rs529657333 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022594 | ATTCCAATGTAATGT[C/T]TGGAAGCCACGGCAC | 55819 |
| rs529678876 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972450 | ACTTGGCTGACTGAC[A/G]GGTAATGGAAGACAT | 55819 |
| rs529682371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180028762 | ATAGCAGGTATAAAT[C/T]GATACCTGTTGATTA | 55819 |
| rs529690804 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180070585 | CCTCTCAGCATTCTC[A/G]GGGTGACAATGAGGG | 55819 |
| rs529708067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180013559 | GCAGTGTTAAGAACC[A/G]TATTAACTTGTCTGA | 55819 |
| rs529716189 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990276 | GTGAGTCACATGTCC[A/C]CTGGACAGGGGGCCC | 55819 |
| rs529718024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180063308 | TCAAACAACAGATAC[A/G]TACGATCCATTCTAG | 55819 |
| rs529725717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932897 | CTGTAATTTTCTTTC[G/T]TGTAATGCCCTTGTA | 55819 |
| rs529764123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926373 | ATCTCAGGCCGGGTG[C/T]GGTGGCTCATGCCTA | 55819 |
| rs529775570 | in-del | -/A | 0.256061 | 0.249927 | intron-variant | RNF130 | GRCh38.p7 | 5:180011766 | AAGACCCTGTCTCTT[-/A]AAAAAAAAAAAAGTT | 55819 |
| rs529801154 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179972500 | TCAAGGCTCTGGTGC[A/G]GGAATGGGAGGCATC | 55819 |
| rs529828298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180005894 | TAAACCCCAAGGATA[C/T]AGAAATGAATTATCT | 55819 |
| rs529850637 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180025405 | TCAAGTGACAACTTC[A/T]AACAACCCACTTGGG | 55819 |
| rs529863616 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179966688 | ACAGCAACACACATC[A/T]CTTTCTTGGTTACAG | 55819 |
| rs529882943 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179920546 | TTAACTATCCTTCAT[A/C]AGGGGCTCTTATTAG | 55819 |
| rs529908769 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001664 | ATACAGTATTGACTA[C/T]AGACCCTGGGATGGC | 55819 |
| rs529942952 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006713 | TAAATTTGACCACTT[G/T]GAAATTAAAGGTGCA | 55819 |
| rs529947206 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025044 | CAAAAGGACTGTCCC[A/C]AAATACCCCTGCCTT | 55819 |
| rs529954755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999755 | AGAAGTGAAGTGAGT[C/T]TCTTGTAGGTAGCAT | 55819 |
| rs529957763 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180052487 | GAGCAGCGCCTGAAG[A/G]CACTACTAACTCTTG | 55819 |
| rs529961226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000495 | TTTTAATGCCTTTCC[C/G]CTTCTCTCCTTCTGG | 55819 |
| rs530030689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179947739 | TATTATTGTACACTA[C/T]TATCAAACAAAAGTA | 55819 |
| rs530036363 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954628 | AATGTTCTGGAATCT[A/G]ATAGTGGTGATGGTT | 55819 |
| rs530037271 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955162 | TTACAAGTCCCTGCT[G/T]CTGGGGGTGCTGCAG | 55819 |
| rs530041263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180036838 | CTGTCTACCCCCACA[C/T]TCAGCTTAAGAAATA | 55819 |
| rs530048284 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180037529 | CTAGGTTTCCCTTCT[C/T]CACTGCCTTCTTTCT | 55819 |
| rs530049344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948347 | GGAATGGTGGTCTCT[G/T]TTTCACCGGGACTCT | 55819 |
| rs530051555 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930269 | CACCACGTTGGTCAG[A/G]CTGATCTCGAACTCC | 55819 |
| rs530105001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958156 | TGCTGGGATTATAGG[C/T]GTGAGCCACCGCGCC | 55819 |
| rs530140888 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972194 | CCAGCAGGGGTCAAG[C/T]GCACTAATGCTGGCT | 55819 |
| rs530145167 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179993053 | TAAAAAGGACATGAA[C/T]ACATCCTTTTTTATG | 55819 |
| rs530206374 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179979233 | AGCCGTTTTGATGCT[G/T]CTTCTATTTTCTTAA | 55819 |
| rs530212866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065255 | GTAAAAATTAACAAT[A/G]ATTTTTAAGAGAAAT | 55819 |
| rs530214702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986142 | TTCCTTATAGAAATC[A/C]TGCACCCACATAAAG | 55819 |
| rs530221580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031379 | GTAATCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 55819 |
| rs530233994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023479 | AAAATATATGCAAAA[A/G]GAGCCTGGCACATCT | 55819 |
| rs530268369 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068213 | TAGTGTGCACACACA[C/T]AAAGCACATTTACAA | 55819 |
| rs530293737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180065896 | TATTCACAACTGCCT[C/T]GGAATAACTTTCAAT | 55819 |
| rs530299500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179928712 | CGGCTCACTGCAAGC[C/T]CCGCCTCCTGGGTTC | 55819 |
| rs530300341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022797 | TGTTTCAAGATTTCA[C/T]CTCCCTAGTTTTGTG | 55819 |
| rs530309003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934974 | TTTTCGCTAGGCTTT[C/T]GAGATTTAAGGTCGC | 55819 |
| rs530314864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974031 | GCAGAAGAGTGCTGC[A/G]GGAGGGGAGGCCTCT | 55819 |
| rs530334891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922192 | TAATTTGCATTCTCT[A/G]ATGACTAGTGACGTT | 55819 |
| rs530347626 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179927954 | CTTTTGTGTCTAGAC[A/T]CTGTCTGACACACAA | 55819 |
| rs530364248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014881 | GTCCCAGATACTCAG[C/G]AGGCTGAGGTGGGAG | 55819 |
| rs530423642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059275 | AACATCATTTCTTCA[A/G]GGACGCCTTGACCAC | 55819 |
| rs530424048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047938 | GACGCTCCCGAGTAC[G/T]CTGCCTTCCCTGGCG | 55819 |
| rs530427817 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179951447 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCATTGC | 55819 |
| rs530429769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945094 | CCAGTTTGGCCAACA[A/T]GGTTAAAAAAATAAA | 55819 |
| rs530438896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041544 | TAAGAAGAAGCCCCC[A/G]GCTGCTCTTCCCACT | 55819 |
| rs530456256 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973851 | GACAGTGAAACCTGA[A/C]AAGCACAAGCATACT | 55819 |
| rs530489474 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945451 | TTCATACAAGGAAAG[A/G]GAAAACATTGCTGAG | 55819 |
| rs530513102 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923457 | TCCTTATATATTTTA[A/G]GTTCGGCCTAAAGGT | 55819 |
| rs530520932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958336 | GGAAGTGTGTGAAAT[C/T]TGTTTCAGTTACACA | 55819 |
| rs530545692 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067636 | AAGTTCAACATAAAT[A/G]TAATTTATTATATAC | 55819 |
| rs530545859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996414 | CATCTTAGTGGAAAC[A/G]TTTTCAGCTTTTCCA | 55819 |
| rs530549550 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921889 | TAGCCAGGCATGGTG[A/G]CAGGTGCCTGTAATC | 55819 |
| rs530619726 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964250 | TGACCGGGTACTTGG[C/T]CACCACAGAGCTGAA | 55819 |
| rs530660196 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064987 | GCTTGCTTCATATTT[A/G]GACCAAGTTGTCTTG | 55819 |
| rs530700535 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022231 | TTTTCCCCTTTGTAA[C/T]TAGTATGTATTCTGT | 55819 |
| rs530701819 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179970284 | TTACATGGTTACATG[C/G]CAAATATAGCCAGTG | 55819 |
| rs530706325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982293 | ATATCCTTTCACCTG[C/T]TGATGGGACATCTGC | 55819 |
| rs530716908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061462 | AACAACATAGTCTCA[C/T]TGTCTCACAGTTCTG | 55819 |
| rs530720430 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986215 | TGTTGGTGTAGCTAT[A/C]GCAATGGCTTCATGA | 55819 |
| rs530720626 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180034258 | TCTAATCCATTTTAT[A/G]TATTACTAGATTCTA | 55819 |
| rs530774531 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965192 | AAGTAAACACCATCA[A/T]AAAACACCCAATATG | 55819 |
| rs530792677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011309 | AAACCCAAAAAAGGT[C/T]TATCAATCAGATAAT | 55819 |
| rs530794245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924087 | TGATGGTCAGTATCT[A/G]TAATCCCAGCTACTA | 55819 |
| rs530803858 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179931072 | ATCAAGAATAGGTGT[A/T]GAATTTTAGCAAATG | 55819 |
| rs530832326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959037 | TAGATATCGCCAGAG[C/G]TCCAGAAATACAGAG | 55819 |
| rs530920214 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062217 | GCACAGCCACGCCTA[A/C/G]ATAATTTTTGTTATT | 55819 |
| rs530941966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925492 | GAGAAGCATGGCTGG[A/G]TTTCTTCTGTTTTTT | 55819 |
| rs530954272 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180049060 | ATAAGCAGAGGCTGG[C/T]AGGCAATTAACAGCT | 55819 |
| rs530971568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012299 | CGTTATACAAAAACT[A/G]GCTTCAAATCACTCT | 55819 |
| rs531037276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990699 | TTCCCAGACACTGGC[A/G]TTACCGCTAGACCAA | 55819 |
| rs531062450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959886 | TTTCCTCATGCCAAG[A/T]TTTTTTTGAATCTTG | 55819 |
| rs531077126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043319 | GACAGAGCAAGACTC[C/T]ATCTCTAAAAAACAG | 55819 |
| rs531098863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991331 | CATGGTGAAGTCCTT[C/T]TGCAATGTATTTGCC | 55819 |
| rs531108394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983209 | TCTAGTATCATATTA[A/G]GGAAGCTTTGCCTAT | 55819 |
| rs531126129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953004 | AGCCAGAACAATTAA[G/T]CATGAGGATAAAATA | 55819 |
| rs531142405 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180043914 | TTATTCAGAAGAAAA[A/T]AAGAGGTTTTCATAA | 55819 |
| rs531153660 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179946716 | CCGCCACCACGCCCG[G/T]CTAATTTTTTTGTAT | 55819 |
| rs531160347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968034 | GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55819 |
| rs531189414 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971433 | GAAGTGCAGTCGTGC[A/T]ATCTCTGCTCACTGC | 55819 |
| rs531199576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940533 | TGAGCCACTGTGCCC[A/G]GCCCAAATTGTTCAC | 55819 |
| rs531199619 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179946814 | CAGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55819 |
| rs531219714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968322 | AACAAACAAAAAAAG[A/G]AGGCGGCGGCTAGCG | 55819 |
| rs531246366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984167 | TGTTGGTCTTTTTCA[C/T]AGATTCCAACATATC | 55819 |
| rs531248672 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015442 | CTTGAAGACTCAAGC[A/T]GGAAAAGGAGTAGGG | 55819 |
| rs531262407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035707 | GGTGTGTCTGACAGT[A/G]TCCCACAGGCATCTG | 55819 |
| rs531313218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180014761 | GAAGCCAGGGCAGGT[A/G]GATTGCTTGAGCTCA | 55819 |
| rs531321369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058876 | GGTATAATGGGTATA[A/G]AGTTTCCATTTTGCA | 55819 |
| rs531337610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962717 | CAAAATGGACCATAA[C/T]AGTCATCTAGCCCAA | 55819 |
| rs531340642 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180061278 | GTCTTTTGGAAAAAA[A/C]CACAACAACTGACGT | 55819 |
| rs531405134 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066004 | AAGGTAATATCACAA[A/T]CATTAAACAGTGTCA | 55819 |
| rs531406972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052842 | TAAGAGGTTTAAAGT[G/T]TTCTTAATCTGAGAC | 55819 |
| rs531426922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994001 | CTTTCCCCATTTCTT[G/T]TTTTTGTCAGCTTTG | 55819 |
| rs531443620 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180053220 | ACCACCTAGAGCTGC[A/G]GAAGAGATCTCACCC | 55819 |
| rs531465923 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955365 | TCCCTGTTCCTCTCA[C/T]GGGAGCCAGGAGCAC | 55819 |
| rs531486025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180046073 | GGCATGGCAGGCCCT[A/G]CCCCATGGGGAGGCA | 55819 |
| rs531501710 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179994427 | TGAAGAGGTCCTTCA[A/T]CCCTTGTAAGTTGGA | 55819 |
| rs531507387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987458 | ACAGGTGTGAGCCAC[C/T]GAGCTTGGCCACCTT | 55819 |
| rs531548178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038487 | GGTGTGAGCCACTGC[A/G]ACCAGCCAAAACAGG | 55819 |
| rs531571155 | snp | C/G | 1.64741e-05 | 0.00286998 | missense | RNF130 | GRCh38.p7 | 5:179980184 | ATGGCTTTCTTGGCT[C/G]CATCTCCGAGACGAC | 55819 |
| rs531592815 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032644 | TGAAAATCAATTGAC[C/T]GTAAAGATATTTATT | 55819 |
| rs531602133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024308 | TTTGGTTAATAATTA[C/T]GTACCAACATTAGTT | 55819 |
| rs531604442 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059143 | CTCCTTTCAAATTCC[A/G]CAAGTACATCACAGT | 55819 |
| rs531644106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937054 | TTCTTAGCTTTGACA[C/G]CTAAAGCATAAGCAA | 55819 |
| rs531645518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979488 | CAGGAGACAGTTTTC[A/G]TTTTATGCCTTTTGA | 55819 |
| rs531648931 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977663 | TTCAAGACCAACTGG[C/T]CAACATGATGAAACC | 55819 |
| rs531656618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016430 | TAATTAGACTGTAAC[A/G]CTGTAAATATCAAAG | 55819 |
| rs531659723 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180031525 | GGGAGGCAAAAGTTA[C/T]ACGTAGCTTTTTGAC | 55819 |
| rs531663680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025097 | CGAGAAGCACTGTAA[A/G]CATCAATGCGGGGTA | 55819 |
| rs531672406 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958003 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55819 |
| rs531715433 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944191 | GGCCAGGCTGGTCTC[C/G]AACTCCTGACCTCGT | 55819 |
| rs531759995 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067325 | CATTAAGATCTTTGC[A/T]ATTCTGACCCTGCTA | 55819 |
| rs531771606 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051459 | TTTCACCATGGTCTC[A/G]ATCTCCTGACCTTGT | 55819 |
| rs531785937 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951635 | ATTCTTAAGTGCACA[C/T]GGAACATTCTCCAGG | 55819 |
| rs531797241 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073721 | GCAAGTACAGACCCT[A/G]GGCCAAAGCAGCGGG | 55819 |
| rs531797606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060358 | CAGTGGCTCCTGGCC[C/T]AGCCAATCAGGAACA | 55819 |
| rs531806081 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976981 | GAGAGGAGCCACAGG[A/C]GAAACCAACATGCTG | 55819 |
| rs531816676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974443 | CACTGAGCCGAGGAG[A/G]AGGCCCCTCCGCCAT | 55819 |
| rs531828303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964020 | GCAGCAGTTCTCCAG[C/G]TCCTGTGGGTGCTCC | 55819 |
| rs531834556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923165 | ATCTAGAAGCTTTAT[A/G]GTTTTAGTTCTCACA | 55819 |
| rs531849033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180010030 | AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA | 55819 |
| rs531858637 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180055476 | TGTGTGTGTGCGCGC[A/G]CGCACGCGTATGTGT | 55819 |
| rs531881619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060018 | AAGTGTCTTTTAAAT[C/G]TGGGTGACAGACGGA | 55819 |
| rs531881891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968893 | CCCCACAAGAAGGGA[C/T]TGTCCAGTCCATGGT | 55819 |
| rs531914889 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179933743 | GCCCAGGCTGGTCTC[A/G]AACTCTTAGGCGCAA | 55819 |
| rs531943198 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928911 | TGGGATTACAGGCGT[A/G]AGCCACCGCACCTGG | 55819 |
| rs531973309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027810 | AGAGAAGAAGCTAGG[A/T]ACCCTGCTAGCTGCT | 55819 |
| rs531985643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180027883 | TCTGTGGCTGCTGCC[A/G]GTGTGAGACTGCACA | 55819 |
| rs532045110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028708 | ACTCGTACATCCTTC[C/T]ACAAATCCCTACAGT | 55819 |
| rs532047450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003437 | TTCCACCTCTGAACT[C/T]TGAACACCTCTTATA | 55819 |
| rs532052722 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932144 | AATTTAAAGTTACCT[C/G]TTATAGGGTGTTCCT | 55819 |
| rs532088973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925647 | AATTGTCTTGCCTCA[C/G]CCTTCCCAGAAACTG | 55819 |
| rs532103962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180057920 | CTACAACCGGTGTCT[A/G]AAGTAGGGGGCGGTT | 55819 |
| rs532109140 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179946605 | GTCGCCCAGGCTGGA[C/G]TGCAGTGGTGTGATC | 55819 |
| rs532153811 | in-del | -/ATC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048793 | AAGAGTCCCCTCTTT[-/ATC]ATAAGATGACTGCCA | 55819 |
| rs532157767 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180062435 | AATCACCACCAAAGG[C/T]CCCACCTCTTAACAC | 55819 |
| rs532158078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966001 | TGGGAAAGGCAACAG[C/T]AGAGCAGCAACCAGG | 55819 |
| rs532160252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021068 | CCTCGCGGGTTCAAC[A/T]GATTCTACTGCCTCA | 55819 |
| rs532171304 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179940456 | TTTTGCCAGGCTGGT[C/G]TCGAACTCCTGACTT | 55819 |
| rs532186435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012650 | TCTGAATAGATAATA[C/T]TTTCCCAGTTCAAAA | 55819 |
| rs532201432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926297 | TTAAAATTTTCTTTT[C/G]AATTTTCCTTTTTCT | 55819 |
| rs532282318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180051113 | TGGCCAATTCTAGTA[C/T]TTTTAAAAAGTAAAC | 55819 |
| rs532283716 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971620 | GTGATCCGCCCGCCT[C/G]GGCCTCCCAAAGTGC | 55819 |
| rs532316533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063230 | AGAAAAAAGGCAGAG[A/C]GACCAAGAAAAAGAG | 55819 |
| rs532361687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954101 | AGGCAGTCACTGGTG[C/T]TATGGAGGTTGTGAA | 55819 |
| rs532366946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180051742 | TTACATCCTTAGAAC[A/G]CAAATATATCTGTTG | 55819 |
| rs532373140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946890 | GCTGGGTTTGCCTTT[A/G]TCTTTCTTTAGCCTC | 55819 |
| rs532390335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961300 | TGAATATTGTCCTTC[A/G]GTGGTTTTGACTGAA | 55819 |
| rs532391710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179954528 | GAACAGGCAAATCCA[C/T]AGAAACAATGAGTAG | 55819 |
| rs532402110 | in-del | -/CTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032701 | ATCTATATGCCTGTC[-/CTT]CTACCAATACCACAA | 55819 |
| rs532408010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005721 | CCTTCTCTGTGAAGT[A/G]TCCTTGACTCCCTGA | 55819 |
| rs532435351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947549 | GTGTTGAAATCCAGC[C/T]TCTGCTACTTACCAG | 55819 |
| rs532472374 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179998833 | ACTGTATTAGAGTTT[A/C]TCTCTCTCTTTAGAT | 55819 |
| rs532494911 | in-del | -/AAAAAC | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056088 | AACTGGGTCTTAAAA[-/AAAAAC]AAAAACAAAAACAAA | 55819 |
| rs532531552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977842 | CTGGGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 55819 |
| rs532555564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044648 | ACCAGCCTGACCAAC[A/G]CAGCGAAACCCCATC | 55819 |
| rs532558260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179975913 | CGTGGCTTTGCAGCA[C/T]GAGAATCGGGCGGGA | 55819 |
| rs532562479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986079 | TTTTAAGTTGTCATA[C/T]AATGACTTTTCTTTT | 55819 |
| rs532572359 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949527 | GAAAAAACAAAGACA[A/G]AACAACCTGTCTCTT | 55819 |
| rs532588992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037434 | GAGGCCTTACAGAAG[A/G]CCTCTATCCTCCAAC | 55819 |
| rs532589898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071344 | CCCTGGCTGGGGCTG[C/T]CGGCCGGGCAGCGCG | 55819 |
| rs532595849 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013890 | CTGAGACAGGGGACA[A/C]ACAGCTGGTAACAGA | 55819 |
| rs532635138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942741 | TCCCTTTCTGAGACT[C/T]CTGGACTTCAAATAT | 55819 |
| rs532640313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985269 | CACAGTTTTCTCCCA[C/T]AGAAATCTTTTGTTT | 55819 |
| rs532672871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978363 | AATTCAGCTCAGAAT[C/T]TTTCTGTGGCTACTA | 55819 |
| rs532696457 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047606 | AAAATTTAGCTTGGC[A/G/T]TGGTGTGTAGGCCTG | 55819 |
| rs532704310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973629 | CCATTCCCGCACGCC[C/T]GACCGCGCTCACCCT | 55819 |
| rs532717356 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942227 | AAAATTAACCAGCAG[G/T]TGTTATTTCTGTACC | 55819 |
| rs532729594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973192 | CTTCTGTGCAACTCA[A/C]CCAGAGATCTTCAGT | 55819 |
| rs532746175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029903 | GCCTAGGCTAGAGCG[C/G]AGTGGCACAATCTCA | 55819 |
| rs532756598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956990 | AAAGTTCTGTACCTT[A/G]TTATTTCTTGTAGTT | 55819 |
| rs532758730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022006 | TCGAAGACTACATTC[A/G]GCCCAGTTGATCTGT | 55819 |
| rs532819880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047122 | GGATTTAGATTCCTC[A/C]ATTGTCAGCTATGGT | 55819 |
| rs532827299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927063 | CTTTTTCTAGTCACC[A/G]TCAGAAGTGGAAATG | 55819 |
| rs532868604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927795 | TAGGCTTTCACCATG[C/T]TAGCCAGGATGGTCT | 55819 |
| rs532887348 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179951453 | CAGTGGCGCGATCTC[A/G]GCTCATTGCAAACTC | 55819 |
| rs532889262 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179924478 | CCAGCCTGCGCAACA[C/G]AGCAAAACTCTGTCT | 55819 |
| rs532889969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988504 | GGGCTCTTCATTTGA[A/G]ATATTTCTAATTGTC | 55819 |
| rs532896682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046355 | AGGCGAGGAGGCACC[A/G]AGAGCGAGCAGGGGC | 55819 |
| rs532916862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040768 | AGCAGCTCGCTGCCA[C/G]CAGAGCTATGAATAC | 55819 |
| rs532927107 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987346 | CTAATTTCTATATTT[A/C]TTGTGGAGAAAGGGG | 55819 |
| rs532932142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963945 | TATAACCTTCTTTCC[G/T]TCTTCATTCTGTCAT | 55819 |
| rs532972685 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938614 | CAAAGACCTAGTTTA[C/T]CAGCTTTACATTTTA | 55819 |
| rs532978085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994691 | ATAACCTCCTGAGAA[A/G]CTGGGGTGGCATGAG | 55819 |
| rs532981796 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995559 | GAGCTAGGACTGAGA[C/T]TGGAGTCCTCTTATC | 55819 |
| rs533036971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981377 | CTGACGGAGCAAGGC[A/G]GGGACCAAAACAACG | 55819 |
| rs533037013 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974751 | AAATGCGAGTGTCAC[A/G]AGATGCCGGCGAGTG | 55819 |
| rs533065104 | in-del | -/AT | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:179924501 | TCTGTCTGAAAAAAA[-/AT]AAAAAATAAATACAG | 55819 |
| rs533120369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179989060 | AATCAACTCAGTTCC[A/G]CATGGCTAAGAAGGC | 55819 |
| rs533129548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970183 | AAGAAAAAAAAAGGC[C/T]TAGTAGAGTTATTTA | 55819 |
| rs533131443 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055145 | GCCAGGAATTTGAGG[C/T]CAACATGGTGAAAAC | 55819 |
| rs533157027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180018617 | GATGAGCTAATCCTA[C/T]TTGTATTATTACTCA | 55819 |
| rs533164172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945371 | GCTTTTCTGGGCTGA[A/G]TGGTACCTGAGCAAG | 55819 |
| rs533168660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033572 | GTGTGCGCCTATAAT[C/T]CCAGCTGCTCGGGAG | 55819 |
| rs533170997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180025273 | CCGTCCTGGAACCTA[A/G]GAAACTGATTTCTAA | 55819 |
| rs533186334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964649 | AGAATTGTGTGTGCA[C/T]AGGCATTTTTCTAGA | 55819 |
| rs533224204 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179935994 | GCAGCACTTAGGTTA[-/C]CCACATGTGTCTCCT | 55819 |
| rs533276243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004177 | GCCCCTAAAAGGAGC[C/T]CTCACATGATTCTTT | 55819 |
| rs533295200 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179941030 | ATTTTTCAGTCCTCG[A/C/G]ATTTCCTTTTGATTT | 55819 |
| rs533317324 | in-del | -/TC | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179969686 | CGCCTGAACATCTTG[-/TC]TCTTCAAAACATAAA | 55819 |
| rs533342941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068453 | CTACACCCACCAATG[C/T]ATTCGACTTAATGAC | 55819 |
| rs533346071 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180060925 | ATACAAAAAATTAGC[C/T]GGGCGAGGTAGTGGG | 55819 |
| rs533358088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048688 | CAGGGCTGTATTTTG[C/T]GGTGAAGAATTCAGC | 55819 |
| rs533378407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042318 | AGAGGTCTCCTAATA[A/C]ATGAAATGGAAGATG | 55819 |
| rs533380765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970854 | CTACAATAGCTAACA[C/T]AGAAAAATGGAGTTT | 55819 |
| rs533382709 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052512 | CTCTTGGGCAGAAAA[G/T]AATGTGGGAGCAAGC | 55819 |
| rs533391611 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923984 | AGCATTTCAGTGCTA[C/G]CTCATGAGCTGCAGG | 55819 |
| rs533409743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180019307 | GAGAATGGCATGAAC[C/T]CGGGAGGCGGAGCTT | 55819 |
| rs533422234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946097 | AAATGCCATTTGGGC[A/G]ATACTGTTTCTTGTA | 55819 |
| rs533431586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924750 | GCCAAGATGGTGCCA[C/T]TGCACTCCACCCTGG | 55819 |
| rs533434024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180061414 | ATTAGTTTCCAGTGG[C/T]GGCCGCAAGACATCA | 55819 |
| rs533496842 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179965081 | TACCTTGTAGAACTT[C/T]GTCACATCTATGCTT | 55819 |
| rs533509308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966750 | CTCTCCTGATGGTCC[C/T]GAATGCCCACATAGG | 55819 |
| rs533531206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005257 | ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA | 55819 |
| rs533543849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179926517 | AGCCGGGTGTGGTGG[C/T]GCATGCCTGTAATCC | 55819 |
| rs533568917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952426 | TGGCTTCCAAATATC[G/T]AAAGAATTAACACAA | 55819 |
| rs533582280 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066633 | CTGAGGTTGGGAGTT[C/T]GAGACGAGCCTGATG | 55819 |
| rs533599051 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179998394 | AATTCCAAAAGTTTC[C/T]ATTGTTACTGATTTC | 55819 |
| rs533599730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180049759 | ATATAGCTGGATTCA[C/T]CTCTATTATTTTATT | 55819 |
| rs533615470 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984382 | AAAAAAGAATTTAGT[C/T]GTTCACCATTAAATA | 55819 |
| rs533630852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952909 | GGTGACAGATGGAAA[C/G]GTTTTCCCTACGAGA | 55819 |
| rs533696355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036148 | GCAACTCTGGATTCT[A/G]ATATTTTCCCCCTTA | 55819 |
| rs533710330 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043239 | CTGAGATGGGAGGAT[A/C]GCTTGAGCCCAGGAG | 55819 |
| rs533721954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179960336 | GATCTGTTTGCAGTG[C/T]TAAAAAAATTTAATG | 55819 |
| rs533751861 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180057844 | TGAGTAGGGCGTTAC[A/G]GGAACCTCCTGAATT | 55819 |
| rs533755239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029275 | ACCAGAAGAAACTGA[A/G]ACAGCTATGGAAACA | 55819 |
| rs533771307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179947797 | GGTATACATTGATAT[A/G]GCATATATATACTGC | 55819 |
| rs533780844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179992437 | GTGAGCCACCACGCC[C/T]GGCCCTAAATCATTG | 55819 |
| rs533829200 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930098 | GTCTTACTCTTGTCG[C/T]CCAGGCTAGAGTGCA | 55819 |
| rs533847053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999130 | CAGGTTCAAGCGATT[A/C]TCTGCCTCAGACTCC | 55819 |
| rs533853600 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180051319 | CAGTGGTGCGATCTC[A/G/T]GCTCACTGCAAGCTC | 55819 |
| rs533908213 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179934354 | TAACCCCCTGGTAAT[C/T]GCTCCTCTGCACTCT | 55819 |
| rs533911008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991904 | GCATTAGATTCTCAT[A/G]AGGAGCACTCAACCT | 55819 |
| rs533930380 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033134 | GAATACTGCTACACC[C/T]GGCTACTTTTTTTAT | 55819 |
| rs533931388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044337 | CAAAATATTTTACTA[C/T]AGAACTTAATTTTTT | 55819 |
| rs533945901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935075 | ATGAAACATTTTAAA[A/G]TAATTTCCACTGCGA | 55819 |
| rs533952108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064634 | TCATTTTCCTCTGTT[C/T]TTAAACCTTTCTAGC | 55819 |
| rs533969110 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944857 | CTTTCCTCCTAATTT[C/T]TCTGCATTATTTCTA | 55819 |
| rs533981334 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179928135 | GGAGGCTCTCTGAAT[C/G]TTGCTGTTAGGGACA | 55819 |
| rs533993513 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180065448 | CCCACTTGGGAAGCT[C/G]TACAAAGAAGTGGTT | 55819 |
| rs533995080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030700 | TGCAATTAATCTTCA[C/T]GCCCAGCTCTACCCT | 55819 |
| rs534005139 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179984486 | GACTTCGGCAAATAT[A/C]TTTTCTCCATCTATT | 55819 |
| rs534009788 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015000 | AAAAAGAAGAGAAAT[A/C]CAACAGTAAAAGGAG | 55819 |
| rs534016856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973706 | CAGGAGGCCTCAGAA[A/T]GAGGCACCTGGGGCA | 55819 |
| rs534017915 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988429 | TTTATTATTTCTTTC[A/C]TTCTACCAATTTTGG | 55819 |
| rs534064542 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961850 | CAATAAAGGCAGATG[G/T]TCATCTGACTCACAC | 55819 |
| rs534069517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977471 | ACTCATGCCTGTAAT[C/G]CCAACACTTTGAGAG | 55819 |
| rs534071571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985539 | TGGCCAGGGGCATTA[C/T]CCAATATCAAAAAAA | 55819 |
| rs534075990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968123 | ACACGGTGAAACCCC[A/G]TCTCTACTAACAATA | 55819 |
| rs534078511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962294 | TTCCAAGTATCTAGC[C/T]CCAGATGAGGTTAGA | 55819 |
| rs534085688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977981 | AGGCCGCGTGCCACA[A/T]CGCATATTGGCTACA | 55819 |
| rs534109218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059364 | TATGATTAAATAATC[A/G]TGTTATGACCTGTGT | 55819 |
| rs534115583 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979553 | CTCTGAATGTAGGGG[C/T]AGCACTAAGATGCAA | 55819 |
| rs534138044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955787 | GCTAGTTCCCAACCC[C/T]TCTGGTAAGGCCAGG | 55819 |
| rs534139361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962945 | GAGATAGCGCTTAGA[C/T]TTATTTTCTCTTCCT | 55819 |
| rs534150047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179978489 | TTTGTTTTAAAAATT[A/G]TAACAATCTATATTA | 55819 |
| rs534205894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002119 | TAGGTACTGGGATGT[A/G]TGATCACTCTGGATG | 55819 |
| rs534209037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014376 | CTGAAGCTGCCGGTG[C/G]CAACATGTAGCTTCT | 55819 |
| rs534245288 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011621 | AAAATTAAAAAATTA[A/G]CCAGTCATGGTGGTG | 55819 |
| rs534247881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179994102 | CTCTGTTTTGGTACC[A/G]GTACCATGCTGTTCT | 55819 |
| rs534250884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179920896 | CTATGTTGATCCTTC[C/T]GAATTTTTTTCAGTC | 55819 |
| rs534259596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007305 | ACGTGTGAGGCTGAG[A/G]CAGGAGAATTGCTTA | 55819 |
| rs534276236 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012205 | AGTCTGCGCTTTTTC[C/T]GCTAGAAAGAGGAAG | 55819 |
| rs534277919 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041315 | GTCACCCCACAACTC[C/T]GTATCAAGATACACT | 55819 |
| rs534296594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938455 | GGGGGTTTCTTTTTG[C/G]GGTGATGAAAACGTT | 55819 |
| rs534319290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025587 | ATTTTTATTTTTTTA[A/C]AGCTACTGCTTAAGT | 55819 |
| rs534328353 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180018046 | CACACCTGTAATCTC[A/T]GCACTTTGGGAGATC | 55819 |
| rs534336841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037255 | GAGAGTAACAAGGGT[A/G]GAAAGAAGGACAGAG | 55819 |
| rs534338753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067693 | TATGTTAAAATTTGA[C/T]TTTTAGAGCCTCCAG | 55819 |
| rs534369242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068158 | ATCAACACAGGGCTT[C/T]CTCCTCTCCCAACCC | 55819 |
| rs534371199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179923461 | TATATATTTTAAGTT[C/T]GGCCTAAAGGTTTCT | 55819 |
| rs534373752 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180066141 | ATTTTGAATTGTACT[C/T]CCATAATTTCCACAT | 55819 |
| rs534374000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060773 | TAAGAACCACTAACC[G/T]AGATGAAGATACAGA | 55819 |
| rs534375789 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180007910 | GCTTGCCTGTCAACA[A/C]CACCACTCCAGAGCA | 55819 |
| rs534382141 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179946441 | AAAAGGGACTTTTAT[-/A]AAAAAAACTTTAAGG | 55819 |
| rs534399134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969890 | CAGCTACTCAGAAGG[C/T]TGAGGCAGGAGAATC | 55819 |
| rs534439722 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180043302 | TGCACTCCAGCCTGG[C/G]TGACAGAGCAAGACT | 55819 |
| rs534443646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008746 | CAAGTTAGCCGGACA[C/T]GGTGGCATGCGCCTG | 55819 |
| rs534467499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993395 | CACCTGTTGTTTCCT[A/G]ACTTTTTAACAATCA | 55819 |
| rs534485251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045686 | TTAGACACAGAGTGC[C/T]GATTGGTGCATTTAC | 55819 |
| rs534494051 | in-del | -/TGTC | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:180055497 | GCGTATGTGTCTGTG[-/TGTC]TGTCTGTCTCATGTG | 55819 |
| rs534516437 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000631 | ATTTCAAATAACCTA[G/T]CTTCAAGTTGAGAGA | 55819 |
| rs534522588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986452 | CAAGATTCATGATAC[C/T]GCACTAAACACATTG | 55819 |
| rs534539573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038176 | CCTCTCACCCAAGCC[A/G]CCCAAGCAGCTGGGA | 55819 |
| rs534572440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996626 | CATTTATGGATTTGC[A/G]TATGTTGAACCATTC | 55819 |
| rs534619770 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990425 | TAGAGGGCGGAGCCA[A/G]GTGTACAGGATGGAA | 55819 |
| rs534622618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026409 | GACAAGTATGCATTA[C/T]TGTAAACTATCCAAG | 55819 |
| rs534633354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989810 | TTTTATTTTTTCTTC[C/T]GTCTTTGTGGTTTCA | 55819 |
| rs534648912 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179959157 | ACTAAGATCTTGGTA[A/G]GCATTCAATAAACAG | 55819 |
| rs534659697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951758 | GAAATTGGAAATCTA[C/T]AACAGAAGGAAATTT | 55819 |
| rs534672802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945872 | AGCCTGAGCTGCATG[C/T]ATTTATACCCACTCA | 55819 |
| rs534679825 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962301 | TATCTAGCCCCAGAT[A/G]AGGTTAGATTGAATA | 55819 |
| rs534690267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018858 | ACCCTCTTGGCTTCC[C/T]TCCACTCCTCCTGGG | 55819 |
| rs534724621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970353 | ATTATGTTATATTGT[A/G]TTACACATACATATA | 55819 |
| rs534796312 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179975982 | GATGCTTCTGAAAGC[C/G]TCCCACTGACTCTGA | 55819 |
| rs534798231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983251 | AAAGACTTCCCCGTT[G/T]TCTCTTCTAGAAATT | 55819 |
| rs534801281 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936381 | TGCTGGACCCATGCT[A/G]GCTAATATTTTATAT | 55819 |
| rs534809825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924221 | AAAATTACTGCTGGG[C/T]GTGGTGGCTCACGCC | 55819 |
| rs534839892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027538 | CTGTGCTACTTAACC[C/T]GCACTTCTCACCCCA | 55819 |
| rs534848753 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006404 | ATTTCCACATTCTGA[C/T]AGGCAAATGCATTCT | 55819 |
| rs534871574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180004285 | CTCACTGATATTCTC[C/T]GTACTTCACACTGTG | 55819 |
| rs534874746 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971405 | GACGGAGTCTTGCTC[A/T]GTCGCCCAGGCTGAA | 55819 |
| rs534901164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020054 | CAACAAAACTAAATG[A/G]CAGGAAGAGAGGGGG | 55819 |
| rs534921056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925358 | GACTGGGATACTTCG[A/G]GGATAGCTAAACACG | 55819 |
| rs534939363 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997383 | GGCTGGAGCGCACTG[C/G]CGCAATCTCGGCTCA | 55819 |
| rs534943269 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179939144 | ATCGCTTGAACTCGG[A/G]AGGCAGAGGTTGCAG | 55819 |
| rs534959901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013001 | TAAGATGCATGGTCA[C/T]GACAGATGACTGTGA | 55819 |
| rs535036048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034712 | CATCTGGGAACATGG[C/G]TTTGGGGAGGATTCC | 55819 |
| rs535085323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000716 | TCATTCATTGAATTC[C/T]TCAGCTGCAGGATTT | 55819 |
| rs535123092 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179993254 | AGTAATGGGATGGCT[A/G]GGTCAAATGGTATTT | 55819 |
| rs535136737 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952400 | CCTACAAAGAAAAGT[C/T]CAGGACCAGATGGCT | 55819 |
| rs535156654 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035245 | TTTCGTTTGGTTCCA[A/C]ATGTTTTTAAAATTT | 55819 |
| rs535158748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940138 | GACCTTCATAGTGAC[C/T]GCTGTGCTTAACAGA | 55819 |
| rs535194549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986993 | ATACTAACTTTTGTA[A/C]ACAAACTTTGTATTC | 55819 |
| rs535206813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931625 | ATAGAAAAAATTAGC[C/T]GGGCGTGGTGGTGCC | 55819 |
| rs535241707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070076 | CAACAGCTTGCCTCC[C/T]CTTCCTCTTTCTACC | 55819 |
| rs535246763 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179932407 | GGACTACAGACATGC[A/G]CCACCACTCCCGGCT | 55819 |
| rs535271950 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034921 | TCCTTTTTTAGTTGT[C/G]ATTTTGGTAAACTGT | 55819 |
| rs535275702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925852 | TTATTCTGAGCCAAG[C/T]TGGAAGACGTAGGCC | 55819 |
| rs535294879 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062862 | CAATCTGTCCCGTTA[A/C/G]CTGGCCATTTTACAG | 55819 |
| rs535321987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979651 | AGGTCTCCGCCACAG[C/T]ATCCTGACACTGCCT | 55819 |
| rs535343276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928897 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA | 55819 |
| rs535370845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966196 | TGCTAGTCGACAGTG[C/T]AATGTGAAGACGTTC | 55819 |
| rs535382221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974202 | TCTCTATGGACCCTC[A/G]GCTGCAGTGGAGCCT | 55819 |
| rs535389195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948057 | GGAGGGTATAAAGTA[A/G]TTGGGAGCATTGACT | 55819 |
| rs535466444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038004 | AGTTACATGGTCAAA[C/T]AGGTTTGGGAAACAC | 55819 |
| rs535554393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004187 | GGAGCTCTCACATGA[C/T]TCTTTTGTATACTAA | 55819 |
| rs535557378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978774 | AATGGGAGCTGTGAA[C/T]CTGGTCACAGATTTG | 55819 |
| rs535576072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938888 | GCCGATTCATGCTGG[C/T]GTTAGGGTACAATCT | 55819 |
| rs535578497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943023 | AACATGGTGAAACAC[C/T]GTCTCTACTAAAAAC | 55819 |
| rs535580451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038629 | AGGAACATATCTAAA[C/T]AAACTAACATTTCAA | 55819 |
| rs535595957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994988 | GACTGGTGGGGAGAG[G/T]TGAAGCTGGGTAGAG | 55819 |
| rs535613265 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030555 | TATTTTTGTTTTTTA[A/C]AAGATGGGGGTTTTG | 55819 |
| rs535623655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935374 | TATATATGTTAATTA[C/T]ATCTTGTCTGTTAAT | 55819 |
| rs535624923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179957272 | CAAAAATTAGCCAGG[A/G]GTGCTGGCAGGCGCC | 55819 |
| rs535632961 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179950462 | TTCTGGTTTTAGGAA[A/C]AAAAATACATGTTTA | 55819 |
| rs535655798 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180029380 | ACTGAGAACAGCATG[-/A]AACCAAGAATTTATT | 55819 |
| rs535663802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936277 | GGTAATTAAAAAAAA[A/T]TTTTTGTAGAGACAG | 55819 |
| rs535674568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041024 | ACTCTTACTCATTCC[C/T]GTTCATGTACTAGCC | 55819 |
| rs535682823 | in-del | -/G | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015479 | GTAGGGAAAGGAGTA[-/G]GGAAAGGAGTAGGAA | 55819 |
| rs535692600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936184 | TGGAGTGCAGAGGCA[C/T]GATCATGGCTCACCA | 55819 |
| rs535712503 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961835 | AATTCACTTCCCAGA[C/T]AATAAAGGCAGATGG | 55819 |
| rs535778913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033314 | CTCTCAGTAATGTTT[A/G]TAGGTTCAATGTGCA | 55819 |
| rs535781377 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036984 | ATACCTATATACATG[C/T]TCTTAAATGACTTAA | 55819 |
| rs535784968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937628 | AATGGTTTAGCCATT[A/G]TGTAAAAGAGTTTGG | 55819 |
| rs535789998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066756 | GCAGGAAGGCGGAAC[C/T]CGGGAGGTGGAGGTT | 55819 |
| rs535795221 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985210 | TCATGATTTCCTTGA[C/T]TGGCTCTATCATAAA | 55819 |
| rs535807804 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180074094 | TGTTAATCAGGTGGG[G/T]AGGAAGTGGCTTTCT | 55819 |
| rs535810719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968995 | GGCATTACTGCCCAA[C/G]TGTATACACTGAAAC | 55819 |
| rs535820981 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180053918 | CACTGCAACCTCTGC[C/T]TCCCAGGTTCAAGCG | 55819 |
| rs535821383 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179963058 | CCTGACCACAGGCAC[A/G]GCCGCCGGGGCTTCC | 55819 |
| rs535830780 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973593 | GGGCCATCACACGGG[-/C]AGAGCGGCCCCGCCA | 55819 |
| rs535835051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020646 | TCAATCACATACAAG[C/T]AGGGCCAAGGGGCCA | 55819 |
| rs535856025 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179997202 | GCTGGAGTGCAGTGG[A/C/T]GTGATCTTGGCTCAC | 55819 |
| rs535871317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922883 | AGGCTGCAGTGAGCC[A/G]AGACTACACTACTGC | 55819 |
| rs535892234 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072293 | GTTGTTTCTCTGTCA[A/G]GCGTGATAGCCGCAG | 55819 |
| rs535914060 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946763 | GCTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT | 55819 |
| rs535927811 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179956617 | CAAACCACACAACTC[A/G]CTGATCCTGCTCTGT | 55819 |
| rs536028634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051258 | TATTTATTTATTTAT[C/T]TATTTATTTGAGACA | 55819 |
| rs536028903 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069430 | CCCACCCCGAGAAAA[C/G]CTGGAGCAAGCCCCT | 55819 |
| rs536038562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047512 | CACTTTGGGAGGCCA[A/C]GGCAGGCAGATCACC | 55819 |
| rs536066341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032440 | GCAGTGGTGCCATCA[C/T]GGCTCACTGCAGCCT | 55819 |
| rs536068834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951160 | GCAGCTTTAAAACAT[A/T]CTTCAACCCCGTATG | 55819 |
| rs536079870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035384 | TTGTACAATTTCAGT[C/G]TTTGAAAATATATTC | 55819 |
| rs536086357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988013 | TTCTCTCTTCTTTCA[C/T]TTTTTGAAATAGTTT | 55819 |
| rs536103754 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950280 | TGCCACCACGCCTGG[C/T]TAATTTTTGTATTTT | 55819 |
| rs536149665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988598 | GTTTTGGTATGTTTT[A/G]TTTCCATTTTCATTT | 55819 |
| rs536149699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980654 | TGACCGCTCCTTGAA[A/G]TTGCTTATCGCATCA | 55819 |
| rs536159481 | in-del | -/AAAG | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180055536 | CCAGTTGTCCTAAAT[-/AAAG]AGAGGGATTTCTGAA | 55819 |
| rs536160211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981238 | AAGCTTTGTGCATCA[C/G]AGGGCCCTAGGAACA | 55819 |
| rs536175009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947013 | TCTCAACACCTCTCT[C/T]CCTGAGGATGCACTG | 55819 |
| rs536181404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945113 | TAAAAAAATAAAGTG[A/G]TAACTGACTAGTATT | 55819 |
| rs536193947 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974437 | CGTGATCACTGAGCC[A/G]AGGAGGAGGCCCCTC | 55819 |
| rs536220443 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062760 | TTGTTCAATCTTAAC[C/G]TGTACAAGTATCTGA | 55819 |
| rs536226445 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966703 | ACTTTCTTGGTTACA[C/G]TCTGTGTTGCAGGCT | 55819 |
| rs536240577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925266 | GAGGGGCTGAAAGTT[A/G]AGTTGATCGCCCATG | 55819 |
| rs536264752 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071006 | CAATTTACCACTTAA[C/G]AAAAACGGCACGTTT | 55819 |
| rs536304594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179934197 | GTTGGCGCATAGCAG[C/T]CTGGCGGCATGGAAA | 55819 |
| rs536316629 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994721 | GCAATGGTGGTAAAA[G/T]AAGTCATGAGAAGCT | 55819 |
| rs536331503 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016335 | TCTGAGGAGCTCTGG[-/C]CCAGTTTCACGCCAA | 55819 |
| rs536344849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977913 | AGATAAACGAAACCA[C/T]AGAACAAGAATTCTC | 55819 |
| rs536353471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973420 | TTTTCTTCCCTTCTA[C/G]GCAAAGTTCTGCTAC | 55819 |
| rs536390022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960263 | TATATTTACCTTGCA[C/T]TTATTCACTTCTTTG | 55819 |
| rs536417552 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179967405 | ATAGAAAACACCTCT[C/T]TCATCCTACTAACTT | 55819 |
| rs536427491 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179998330 | CTAATTTACTCATTG[A/T]CCCACTGGTTGTTTA | 55819 |
| rs536471786 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179925384 | ACACGTAGAGGTACC[A/G]GTAGGGGAGGGCACT | 55819 |
| rs536474850 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004944 | CCCATTTTTTTTTCT[C/T]AAAAGAAGCCTCTGT | 55819 |
| rs536490680 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053279 | AGGACAGTGGCCAGG[C/T]ATATCCCGGTGAACA | 55819 |
| rs536503520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180007773 | TGTTTCCTCCTTCAT[C/T]AGCCCCGGCCCCACA | 55819 |
| rs536505229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991757 | CCCTTTATTTCTATT[A/G]TTATTAAATTGTAAT | 55819 |
| rs536508966 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179983705 | TACAATGAGATTGTG[C/T]TGAATGTATACATCC | 55819 |
| rs536511814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180058952 | TTACCATGACTTAAC[A/G]GTTAGATGGTCAATT | 55819 |
| rs536535642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179961720 | ATAAGCAAAAGAGGT[A/G]GCTGTGGGTGAAATA | 55819 |
| rs536542335 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922041 | AGAAAAAAAAGGAAA[A/G]AGAAAAAAAAAGATG | 55819 |
| rs536548437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052876 | CATAAACCAATAAAT[A/G]CAAGTAATAAGAAAA | 55819 |
| rs536555471 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057085 | TTCAACCATACCAGC[A/G]TCTGTGCTAATAAGG | 55819 |
| rs536638499 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992280 | CCGAGTAGCTGGGAC[C/T]ACAGGCACCCGCCAC | 55819 |
| rs536655090 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179977901 | CAAACATAAAAAGAT[-/A]AAACGAAACCATAGA | 55819 |
| rs536666649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937571 | AGTGTTGGCAAGGAG[G/T]TAGCAAATCAGAACC | 55819 |
| rs536667566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933479 | TTTCTATTTATTTAT[C/T]GTGGTTTTTGTCCAT | 55819 |
| rs536672871 | snp | G/T | 0.000116243 | 0.00762287 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015268 | CCCTTTAGAAATCTC[G/T]TAAAATGTTGTTCAA | 55819 |
| rs536683021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980428 | TCAAACAGAAATATA[C/G]AACTATAGGTCTTCA | 55819 |
| rs536704047 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073922 | TCTTCCCGGTGACGG[C/T]CTCCTGCTCTTCTTG | 55819 |
| rs536707646 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179926592 | GGTGGAGGTGGCAGT[A/G]AGCCGAGATAGCGCC | 55819 |
| rs536716743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022078 | TGGCAGTAACAACAC[A/G]GAGGTGAGGCTGCGC | 55819 |
| rs536745459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972769 | AGAAAGAACCAAATG[A/G]TATAATCCTCATATT | 55819 |
| rs536761345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969114 | CTTTTTGTTCCATAA[A/G]GAGATCATTCTTTCA | 55819 |
| rs536788581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067537 | AGTGGTTTTTAAAAA[A/T]ATTCAAATATTTATA | 55819 |
| rs536790941 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968137 | CGTCTCTACTAACAA[C/T]ACAAAACATTAGCCG | 55819 |
| rs536796933 | in-del | -/TAAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044045 | CATGACTGATGACTA[-/TAAT]TAAGTAGTATTACTC | 55819 |
| rs536824995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014343 | CTATCAATCTATCAG[C/T]GATTGTCCTTTCATA | 55819 |
| rs536831902 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920073 | GCCAGCCTTGCTGGG[C/T]GCCCACCTTCAATGA | 55819 |
| rs536833870 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180058471 | AGGAACTAACCTAGT[C/T]GAATTCATAGAGACA | 55819 |
| rs536853920 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041889 | TGAGACCACCCTGGG[C/T]GACAAAGTGAAACAA | 55819 |
| rs536876125 | snp | A/T | 0.0494327 | 0.149241 | intron-variant | RNF130 | GRCh38.p7 | 5:179920801 | TATATATATATTTTT[A/T]TTTTTGAGATGGAGT | 55819 |
| rs536896894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007243 | CCATCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 55819 |
| rs536898046 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921490 | GAACTTTTTCAGAAA[C/T]TGCCAGGCTGTTCTA | 55819 |
| rs536911692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055701 | CCCTCATCAAATGGA[C/T]AAATGCCTTTTTTTA | 55819 |
| rs536916899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052117 | CACTTTCCACTGCTA[A/G]ACCCTCGCCAAGGTC | 55819 |
| rs536917153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003187 | TTTAGCAGGTAAAAC[C/T]GACAGAACCTCATGA | 55819 |
| rs536918598 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006928 | AGATACATTCTGACA[C/G]TTTTCCAGGAAGAGC | 55819 |
| rs536930640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964277 | TGAAAACCTCTGGTG[C/T]TTACAACAATAAGGA | 55819 |
| rs536949198 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994227 | TGAACTTTAAAGTAG[-/T]TTTTTTTCCAATTCT | 55819 |
| rs536991487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045005 | CATGGAACCCCTGAA[A/T]CTTGCGCAGCCAGGA | 55819 |
| rs536991992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958067 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTTT | 55819 |
| rs537002467 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954863 | GCAAACATTTACAAA[C/T]ACTGAAAATCCTTCA | 55819 |
| rs537026399 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179995970 | GGGGGAAAAACCCAT[A/C]CAAAGATTGTGTTTT | 55819 |
| rs537063797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033098 | CCCACTTCAGCCTCC[C/T]GAGTAGCTGGGACCA | 55819 |
| rs537087633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996558 | TGCTTTTTCTGCATC[C/T]ACTGGCATTACCACA | 55819 |
| rs537114880 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940875 | CTAAAGACTCATGCC[G/T]TTTTCTGTATTTTTC | 55819 |
| rs537187041 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041567 | TTCCCACTCCCACTT[C/T]CACATTTATAACAGG | 55819 |
| rs537226841 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947631 | GTAAAACGGAGTTAA[C/T]AAGAGGGTTGTTGCA | 55819 |
| rs537240119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923028 | TATAACAATGTCTTT[C/T]GAAGATTAAAAGTTT | 55819 |
| rs537246041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180026721 | AATTTTAAAATTAGG[C/T]ATAAAACATAGCCTT | 55819 |
| rs537258291 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060610 | CCACCCTAACTTAGC[A/G]CAGGGATTCTTAACT | 55819 |
| rs537279817 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179975257 | CGAAGGCGCAGCTGC[A/G]AGTGGCATCTGCTGG | 55819 |
| rs537344523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047697 | TGCAGTGAGCCGAGA[C/T]TGCACCACTCCACTC | 55819 |
| rs537353013 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056121 | AAAAAAACAAACAAA[A/C]CATCACCACCAATCA | 55819 |
| rs537376612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019862 | CACTCAAGCACTGGG[C/G]AGCCACATGGCCCTG | 55819 |
| rs537382465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061987 | CCGCTGTCTGCTTCA[A/T]CAATGGAGACTTCTT | 55819 |
| rs537398478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961627 | TGTAATTATTTGCTT[C/G]TACTGGTTATCACTC | 55819 |
| rs537409079 | in-del | -/T | 0.216048 | 0.247684 | intron-variant | RNF130 | GRCh38.p7 | 5:179946555 | CACACCCACCGGGGA[-/T]TTTTTTTTTTTTTTT | 55819 |
| rs537411611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958619 | GAAGAATCAGGTCCT[A/G]GTGCAGGCTCGCTAG | 55819 |
| rs537418753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007133 | GGGCCAGGTGTGGAG[A/G]TTCATGCCTGTCATT | 55819 |
| rs537420814 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954936 | ATCAGTAAAGCAAAA[G/T]TATTTCACCGGCACA | 55819 |
| rs537426103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999213 | TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG | 55819 |
| rs537434817 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180003689 | GTCTAAAAGCCACTA[A/T]TTTTTTAAAATTTTT | 55819 |
| rs537466124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041833 | GTTAATCCCAGCACT[G/T]TGGGAAGCCGAGGCA | 55819 |
| rs537472032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951574 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 55819 |
| rs537488604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999965 | ATCATTAAGGTTTGG[C/T]GGTTTACTGTAGTGC | 55819 |
| rs537499137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992587 | TTGGAGAATTACTGT[G/T]TTTTTTTGGGGGGGT | 55819 |
| rs537514379 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021251 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 55819 |
| rs537523042 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040916 | AAAATAAAAAAGGAC[C/T]GATAATATCCAGTAC | 55819 |
| rs537562705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993197 | CATACGTGTGCATGT[A/G]TCTTTATAGCAGCAC | 55819 |
| rs537578707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180042492 | CAACTATTGAAAGAC[A/C]CAGACGATGCACTAT | 55819 |
| rs537622851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939572 | AGTGATGTTTCTGCC[A/G]TTAACCATTTCTAGT | 55819 |
| rs537627645 | in-del | -/AGAA | 0.00260999 | 0.0360303 | intron-variant | RNF130 | GRCh38.p7 | 5:179920443 | TGGAAAAGGAAGAAG[-/AGAA]AGAGACTTAATAGGT | 55819 |
| rs537659993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940063 | ATCTGGGTGCCACAT[C/T]GGTGTCATTCTCCAA | 55819 |
| rs537704907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179931418 | AGTGTAGCTTTTTTG[C/T]TTTTTGTTTTTTTTC | 55819 |
| rs537745502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975912 | GCGTGGCTTTGCAGC[A/C]CGAGAATCGGGCGGG | 55819 |
| rs537752377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971324 | AGACGTTCAGGGCAG[C/T]TTTGGAAGAAACACT | 55819 |
| rs537775625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023073 | GTAAATAGATGTAGG[A/C]TGGCAAGAGCCAGGT | 55819 |
| rs537779046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069910 | GGGCTTTTGTTTGGG[C/G]TGACAGGCAAGCAAC | 55819 |
| rs537789852 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929875 | TAACACCTCCATAGT[A/T]TCGTGTCACTCATTT | 55819 |
| rs537790893 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941893 | ACTGAAACTGATTAA[C/T]GGAATTTAAAAAATG | 55819 |
| rs537827001 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051973 | GCAATATAAGTGTTA[A/C]TTGTTTATCCACATC | 55819 |
| rs537828495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066083 | GTGTACACATACACA[C/G]GCCCTCTGATATGGT | 55819 |
| rs537835723 | in-del | -/ATTT | 0.00359711 | 0.0422566 | intron-variant | RNF130 | GRCh38.p7 | 5:179925509 | TTCTTCTGTTTTTTC[-/ATTT]ATTTATTTATTTATT | 55819 |
| rs537846142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928207 | TTCCCTCGGATGATG[C/G]CTGGGAGTGGGATTG | 55819 |
| rs537854717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015914 | ACCATCCATTCAACA[A/G]TATTTATTGAGCACA | 55819 |
| rs537862958 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069029 | TCAAGATTATAATGT[A/G]AAATACCCAAGTATT | 55819 |
| rs537880958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179921680 | CATGTGCTTGTAGTC[C/T]CAGCTACTTGGGAGG | 55819 |
| rs537882995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928865 | CAATCTCCTGATCTC[A/G]TGATCCCCCTGCCTC | 55819 |
| rs537904389 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979107 | CAAAGTCAGATGGGT[A/C]GGTTAAATCCGCTCC | 55819 |
| rs537911211 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952639 | CAAATATAAAAAGGA[C/T]TGTACATTATGACCA | 55819 |
| rs537970061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179947906 | CATGTAAGAATATGG[A/G]TGTGTATGTGTTTGT | 55819 |
| rs537977469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066349 | ACCATGATTCTGAGG[C/T]CTCCTCAGCCATGTG | 55819 |
| rs537993333 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950000 | CCATTTGTTTGAAGC[C/T]GTTTTCCTGGGTGGC | 55819 |
| rs538001610 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962984 | CTGTCCTAACATCTG[G/T]AAACAGCGGGTCTTT | 55819 |
| rs538012750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046128 | CGCGGTGGACCGCGG[C/T]GCGTGCAGGCCCACA | 55819 |
| rs538013748 | snp | A/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179956541 | ATTACCAGCTCTTTA[A/T]AAGAATCAAGTCCAA | 55819 |
| rs538034799 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982927 | ATTGTAATGATGTTG[A/G]CCATCTTTTCATGTA | 55819 |
| rs538035471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054485 | ATATCCAGTTGTCCC[C/T]GCACCCTTTACTGAA | 55819 |
| rs538037792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942431 | AGAATATATGGTCCG[C/T]ATGCTCTTTTTGGAA | 55819 |
| rs538043257 | in-del | -/TGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982572 | TGAGATTTTGTGTTT[-/TGTTT]TGTTTTGTTTTGTTT | 55819 |
| rs538051231 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050438 | ACATTATGGAGAGCA[A/G]TCTGCTTTATTCGGT | 55819 |
| rs538069968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949607 | TTAAATTTTAATCTC[A/G]AATTTTTTAAATAGT | 55819 |
| rs538071941 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978849 | TAAGAGTGAGAAAGA[C/G]TCAGCCAGGTATTCA | 55819 |
| rs538080838 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023351 | TCTAATGCCCGGATC[A/T]TGGTTTTTAATACCA | 55819 |
| rs538090168 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072438 | AACATTCACGTCATG[A/C]GGTTGACATCATGGA | 55819 |
| rs538093873 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931675 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATTG | 55819 |
| rs538121286 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031225 | GGCACGGTGGCTCAC[G/T]CCTGTACTCCTAGCA | 55819 |
| rs538147467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973763 | ACTCACGTGATAAAA[A/G]CACACATAAATAAAA | 55819 |
| rs538177589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950383 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGTGT | 55819 |
| rs538177706 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179944001 | TTTTGAGACGGAGTC[C/T]TGCTCTGTCACCCAG | 55819 |
| rs538192742 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047827 | CTCCTCTCTCCACTC[C/T]CACGTCCCACTTCCT | 55819 |
| rs538194971 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040046 | GCATTGTTACTACTG[A/T]AATTATATTAATTAC | 55819 |
| rs538214716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059068 | CAAAATCCTAACAAG[G/T]CCTGGAAAACACTGA | 55819 |
| rs538215839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968163 | AGCCGGGCATGGTGG[C/T]GGGTGCCTGTACTCC | 55819 |
| rs538238769 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180027230 | GGAATCAGTGTCTTT[A/C]CAATTAGCTTATGTG | 55819 |
| rs538244896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930671 | AATGTTTGCTGTAGT[A/T]TTGAAAATATCCATT | 55819 |
| rs538252975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179995255 | TCATCCCAACCACAG[A/G]AATCAGACAGACCAT | 55819 |
| rs538257535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010972 | CATGCCAATTTCCAG[A/G]TTATGATACTGACCA | 55819 |
| rs538278138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180061107 | AAGCTATGTTCATGC[A/G]TTCACTAGTGACACA | 55819 |
| rs538283937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179924387 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55819 |
| rs538293272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179924949 | CATCAGCACAATCCA[A/G]CAGCACTAAGGGAGG | 55819 |
| rs538298885 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179931396 | GTTCTTTTGTGTGTG[-/T]GCTTTAAGTGTAGCT | 55819 |
| rs538298940 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924436 | GGAGGCGGAGGTTGC[G/T]GTGAGCTGAGATTGT | 55819 |
| rs538420448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001528 | TGGGAATTAGGGCAT[A/G]ACACTGGCCTGACTA | 55819 |
| rs538432880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057453 | ACTAGGGAGGCTGAG[A/G]CAGGAAATTGCCGGA | 55819 |
| rs538449958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957201 | TGGATCACCTGAGGT[C/T]AGGAGTTTGAGACCA | 55819 |
| rs538467728 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929565 | CCAGCCTGGGCAACA[C/T]GGCAAAATCCCATCT | 55819 |
| rs538472176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002099 | TGCTGGGAGCTGCTT[A/C]AGCTTAGGTACTGGG | 55819 |
| rs538490404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987249 | CATGGCTCACTGCAG[A/C]CTGGACCTCCTGGGC | 55819 |
| rs538506632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038922 | GGAATGAAGATAAGT[G/T]ACATTAGGCCCACAT | 55819 |
| rs538568333 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021103 | TCCAAGTAGCTGCAA[C/T]GTCAGACACGTACCA | 55819 |
| rs538574170 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179946525 | TTCTTAGTCTTAACA[A/G]ACCGACCAGTACAGC | 55819 |
| rs538576312 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923240 | AAGAGTTGAAGTTCA[-/T]TTTTTTTTTTTGCAT | 55819 |
| rs538604008 | snp | C/T | 4.97574e-05 | 0.00498761 | missense | RNF130 | GRCh38.p7 | 5:179970433 | CCAGGGCCTTCAATA[C/T]ATTAAGTTTGCACAT | 55819 |
| rs538639818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946667 | CACGCCATTCTCCTG[C/T]CTCAGCCTCCCGAGT | 55819 |
| rs538651861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068843 | GTTTTTCCACCAGGA[C/T]CTGTCTGATAACTTT | 55819 |
| rs538674459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035858 | GGCTCGGCTCTTTTA[C/T]AGAATTTTTATGTTC | 55819 |
| rs538710197 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180070199 | ACTGGCACAGAGCAG[A/G]AACGCAAATATTTAC | 55819 |
| rs538724116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941547 | CAATAAGACTGCTTG[A/G]GCTCTCCTTCTCTCT | 55819 |
| rs538731105 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997678 | TGCCATGTTACCCAG[A/G]CTAGTCTTGAACTCC | 55819 |
| rs538747883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977264 | GCACAAAGCAGGTAT[A/C]AGTTCTTTCCATTTT | 55819 |
| rs538855029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933211 | GTTAAAAAGAATTCA[C/T]CAATGAAATCATCTA | 55819 |
| rs538890711 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969214 | TTAAGCAAGGGCTAA[C/T]GAAGGTCCTTGGTTA | 55819 |
| rs538914621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969984 | CAACAAGAGCAAAAC[C/T]CCCTCTCAAAAAAAC | 55819 |
| rs538922704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064206 | ACTGTTTAGTTTGTG[C/T]ACAATCTCAAATTCC | 55819 |
| rs538936438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990967 | TTTATAATATTGGAA[C/T]AGCTCGTGCCCTCGG | 55819 |
| rs538963137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180043567 | CGACAGTGTCACAGT[C/T]CACTCAGAAGACAGC | 55819 |
| rs538975206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035285 | TTTTTTATTGGACCC[A/G]TGTGTTATTTAGATG | 55819 |
| rs538996010 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068332 | TAATAAGAAAGCAAC[C/T]GTGATCTGTGCATAA | 55819 |
| rs539047941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028414 | TTCTCCATTTCCTTC[C/T]GACTCCCTCTCCTCT | 55819 |
| rs539051138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949484 | AGGCTGAAAATACTC[C/T]AGAAAAATACTTTAA | 55819 |
| rs539060772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983518 | ACCATTAAGGAAATA[C/T]AATCCTGTCCTGATT | 55819 |
| rs539063676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179943772 | CAGCTATGATTAAAC[C/T]GCAAAGTATATTTAA | 55819 |
| rs539095020 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947310 | GCCCACAGTAAAGTC[C/T]GTGCCCTGTAACATC | 55819 |
| rs539118802 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945197 | CCTTCCTAAGGGCTG[C/G]AGGAGTTCTCGCCCA | 55819 |
| rs539138001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979809 | TCTCCATGTATCTAG[C/T]GAAAAAATAAAACAA | 55819 |
| rs539148516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980326 | ATGTCCTACATATAA[A/G]AGAATGATAAAATAG | 55819 |
| rs539180736 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945921 | AAAAAGGCGGGGGCA[-/G]GGGATATTTAAATGG | 55819 |
| rs539210382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974516 | GAAAAGGAAACGTCA[C/T]GTGGCAAGAAGCAGG | 55819 |
| rs539223011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013778 | CATAAATTGGTACTT[C/G]TTGCACTAATCTAGG | 55819 |
| rs539244512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063544 | TGAAGTAAAGATACC[A/G]ATAGGAAGCCAAGCG | 55819 |
| rs539271195 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179926532 | CGCATGCCTGTAATC[C/T]CAGTTACTCGGGAGG | 55819 |
| rs539283640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006178 | AAGAAACATAATGAA[C/T]AAAATTCACTCTGCC | 55819 |
| rs539297895 | snp | A/G | 5.05565e-05 | 0.0050275 | missense | RNF130 | GRCh38.p7 | 5:179966838 | ATTTCTCCTGTTCTC[A/G]GAGTGAGCTCCCCAT | 55819 |
| rs539312870 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920010 | ATTGTTCAGAGATGC[A/G]TCTGCAATGCAACAT | 55819 |
| rs539313330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009810 | ATGTGATTGTTCACA[A/G]CTGCTTTATTTGTAA | 55819 |
| rs539359604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961057 | ATTATCTTTCCTATC[A/T]TCTGCCACAATAAAA | 55819 |
| rs539386506 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180033520 | CTTGAGGTCAGGAGT[C/T]CGAGACCAGCCCGGC | 55819 |
| rs539394685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963660 | ACGAAGCAGACGTCA[A/G]CGGAGGTGTAAGCCA | 55819 |
| rs539407893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002226 | CAAGGTACTGTTTTC[C/T]CAAAAGGCAGGATAC | 55819 |
| rs539407928 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030248 | ATCACCTCATAAATA[C/G]TTGCTTTGTCTCTCC | 55819 |
| rs539424003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002270 | GTCCAAAGCAGCTGG[C/G]GGAAGAACAGGTGGA | 55819 |
| rs539436533 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180039916 | CTGTCTAAAAAATAT[A/T]TTTAAAAACTCATCG | 55819 |
| rs539497793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180003065 | AGAATTAAAATCTTG[C/T]CTCCACAGGATGTCC | 55819 |
| rs539510139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987727 | TCTATTGAGAATCTG[G/T]TATTTGTTGTTCCTT | 55819 |
| rs539514365 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072978 | ATGGCGTTTAAAAGA[C/T]ACACATCGCTATAAA | 55819 |
| rs539517186 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069070 | ATCATTTTCTTAACA[C/T]GAATAATTTTAACAG | 55819 |
| rs539519549 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180047587 | CTGTCTCTATTAAAA[A/G]TACAAAATTTAGCTT | 55819 |
| rs539550356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180023882 | TATGGCAGGGGGAAA[A/C]GAGTTAACTTCACAG | 55819 |
| rs539558009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066248 | TAAGTCTCACCAGAT[C/T]TGATGGTTTTTATCA | 55819 |
| rs539562868 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179988782 | TTTTAAAAATTTGTT[G/T]AGACTTGTTTTGTGG | 55819 |
| rs539569937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032223 | AAATCTAATTTTTTT[C/T]ATAAACAGTGTTTTT | 55819 |
| rs539580843 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049888 | CCTCATCTATATATT[A/C]AAGTTCTATTTTTTT | 55819 |
| rs539598937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033497 | GGAAGGCTGAGGTGG[A/G]CAGGTCACTTGAGGT | 55819 |
| rs539610656 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016122 | GCCGATCGGGCAGGA[C/G]GACAGCAGAACGAAA | 55819 |
| rs539642653 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034631 | AGTATACAGAAAAAA[C/G]TAAACATAGCAGGTT | 55819 |
| rs539667846 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006656 | ACATCTGCCCCGTTC[C/T]TAAACAGTAAAATGA | 55819 |
| rs539690306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180017689 | CCCATCCCCATCAAT[A/T]CTATTTTTTAATGAG | 55819 |
| rs539711172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982369 | TCTCAATTCTTTGCA[G/T]GGACATATGCTTTCT | 55819 |
| rs539757551 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057698 | TCATGGGACCCTTCC[A/T]GACCTTACCCTATGT | 55819 |
| rs539763836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969728 | GGCACGGTGGCTCAC[A/G]CCTGTAACCCCAGCA | 55819 |
| rs539771708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964192 | CGAGGAGCAGCACTG[A/G]CTGTCCAGGCTGTGA | 55819 |
| rs539774808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026553 | AATGACGTCATGGAC[A/G]GGGCACTGGAACAGA | 55819 |
| rs539792537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054908 | TTAAATGATATTGTG[A/C]AATTTTTATTTTCTA | 55819 |
| rs539805445 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939916 | AATGCATTCCACCTC[C/T]TTCCTCTGTCTAATC | 55819 |
| rs539805604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010109 | AAAATTAGCCAGGCA[C/T]GGTGGCAGGCACCTG | 55819 |
| rs539818327 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049807 | ACTTTTCTAAGCTTC[C/T]TTATACTTTTTTTCC | 55819 |
| rs539826424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055609 | TGTTTTCAGATAATA[C/T]TGCCAACAGTATAAT | 55819 |
| rs539832444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923280 | CAATTGTTCCGTCGT[C/T]GATTGTTTAAAAGAT | 55819 |
| rs539929887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043726 | AACAGATTCTATGAA[C/T]AACAGCATGATCAAA | 55819 |
| rs539940227 | in-del | -/TGTT | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180029105 | TCCCAATCTTGTGAC[-/TGTT]TGACATTTATGCCAA | 55819 |
| rs539965730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951285 | TTCCAACAAATTCTA[C/G]AACTACAGAGAAGAA | 55819 |
| rs539966945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940394 | CCCAACTAATTTTTA[A/T]ATTTTTAGTAGAGAT | 55819 |
| rs539976883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041712 | TGCCGGTCCTCTGTG[C/T]GCCGGGAAGGAAGTA | 55819 |
| rs539982305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035558 | CTATATGCTTGCTAA[C/T]TTTCTATCTAGCTAT | 55819 |
| rs539992515 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028649 | CCCAATTACTTCAGG[A/C]GTGTGTGTTTCCCTA | 55819 |
| rs539998228 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928254 | CATATTTTCAGCGTC[A/G]GCAGACACTGGCCAT | 55819 |
| rs540017076 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073718 | TCGGCAAGTACAGAC[A/C]CTAGGCCAAAGCAGC | 55819 |
| rs540025287 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179932055 | CCATCTCTTGCAATA[A/C]ATTTGTTTCCTTTTC | 55819 |
| rs540042224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940809 | CTGCCCCATTCTCTG[C/T]CTTCTCTCCTTCTAT | 55819 |
| rs540061533 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179932798 | CTGAGATTGTACCAC[G/T]GCACTCCAGCCTGGG | 55819 |
| rs540065066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981280 | ACAAGGGGCAAAAAC[C/T]GCGACTGTCCCAGGC | 55819 |
| rs540078889 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057080 | CCCCTTTCAACCATA[A/C]CAGCGTCTGTGCTAA | 55819 |
| rs540098642 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071039 | ATATTAGAAAAGGGC[C/T]GCATCCTTCCAGATC | 55819 |
| rs540135561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063152 | TTAAGCAAGCAGTAA[C/T]ATGACTGGGTGAACC | 55819 |
| rs540155721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180071042 | TTAGAAAAGGGCCGC[A/G]TCCTTCCAGATCTAG | 55819 |
| rs540157561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973063 | ATATTTTTGGTCTTT[A/G]AAAAAAAGTTCCTTT | 55819 |
| rs540172049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063749 | CAAACCTAAGACTTT[C/T]CCCAGCAACACTCAG | 55819 |
| rs540185892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021642 | TTATTATTATTTAAA[G/T]AATCTAAAACTTACA | 55819 |
| rs540228330 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025099 | AGAAGCACTGTAAGC[A/C]TCAATGCGGGGTAGA | 55819 |
| rs540238321 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179946596 | TCTCGCTCTGTCGCC[C/G]AGGCTGGAGTGCAGT | 55819 |
| rs540263295 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998587 | TACATGCAAGCAAAA[C/T]TGTGCCTAGCTGATA | 55819 |
| rs540282868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983082 | ATTATTGACTTTTGA[A/G]AGAACATTATATATT | 55819 |
| rs540310410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961244 | TACACAACATGCACG[C/T]ACACACACACTCTCT | 55819 |
| rs540334082 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179932155 | ACCTGTTATAGGGTG[C/T]TCCTTCAGAAGCAAA | 55819 |
| rs540344349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983928 | CTTAAAATTTAACTT[G/T]CTTAGAGATAGGGTC | 55819 |
| rs540357981 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180046360 | AGGAGGCACCGAGAG[C/T]GAGCAGGGGCTGCTA | 55819 |
| rs540378484 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954946 | CAAAAGTATTTCACC[A/G]GCACATGTAAAATCG | 55819 |
| rs540379343 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004356 | ATCACACACAGAATG[-/T]TTAGAAATGACAAAA | 55819 |
| rs540417670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052274 | TGCTTGACATTTCTC[C/G]ATGAATACTGAGCAG | 55819 |
| rs540439016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045043 | GGATACGCAAGTTGC[C/T]AGCATAAAAACACAG | 55819 |
| rs540460242 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179976940 | ATACTCAGAACTGTG[C/T]ATCTTAGTTTCATGC | 55819 |
| rs540484311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179948210 | TCTCTCATTCAGATA[C/T]TGCGAAGATTAAAAT | 55819 |
| rs540520744 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179992773 | GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA | 55819 |
| rs540520937 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985961 | ATCGTCAAAAGCTAC[G/T]TCTCCTGTTATCTTG | 55819 |
| rs540522277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966496 | GTGTCACCTTCCAAC[A/G]TCTCCCTTTAAATGC | 55819 |
| rs540538164 | snp | A/G | 4.94271e-05 | 0.00497102 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179978223 | GGGGAGAATTCGGAC[A/G]ACATCATTCTGCTTA | 55819 |
| rs540598033 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942651 | CATTTAGGAGAAAAT[A/T]TTCAGGTTACTATGA | 55819 |
| rs540633414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006524 | TATTATATACACATG[C/T]TATGGCAAGAAGCTT | 55819 |
| rs540645681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010064 | CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC | 55819 |
| rs540645913 | in-del | -/CTTA | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179961103 | ATTAAGTAATTCATG[-/CTTA]CTGTTAAAAAAAAAA | 55819 |
| rs540646885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922605 | CAAACCACCACGCCC[A/G]GCTTGGGCTGTCTTC | 55819 |
| rs540647501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060244 | GAGTAAATTGGTGTT[A/G]CTGTGAGCCACCTAG | 55819 |
| rs540654327 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995977 | AAACCCATACAAAGA[C/T]TGTGTTTTCTATTTC | 55819 |
| rs540671673 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958272 | TAACGACTAATATTA[A/G]CAACAAGGCACAGGA | 55819 |
| rs540704527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999496 | GGAAACCAAGACGGG[C/T]GGATCACCTGAGGTC | 55819 |
| rs540709095 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072547 | TTGGCACTGGGGGAC[-/G]GGTTTCCAGGAAGAG | 55819 |
| rs540724733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044560 | TCCACATGGCCGGGC[A/G]CGGTGGCTCACGCTT | 55819 |
| rs540725430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055334 | TTTTTCTTTGAGAAG[A/G]AGTCACTCTGAGCCA | 55819 |
| rs540741754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002481 | ATGGTATAGCACAGC[A/G]GCTGTGTGGGCCACA | 55819 |
| rs540751100 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | RNF130 | GRCh38.p7 | 5:179975034 | AGGTGCTGCTGTGCC[A/G]AATGCGGAGCGCCAG | 55819 |
| rs540751473 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019602 | CAGTTCTTCAAACCC[A/C]ATCTTCATTCTTCTC | 55819 |
| rs540760436 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007817 | AAAGCACTATCTTCC[A/G]ATAGCAGGCTCCTGG | 55819 |
| rs540773781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947511 | AATGGGGTTTGGAAC[A/G]CAGACCCTGGGGGCC | 55819 |
| rs540779080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958122 | GACCTCGTGATCCGC[C/T]CGCCTCGGTCTCCCA | 55819 |
| rs540796048 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180036603 | TTGTCCCTTCATTAA[C/T]ATCCAGAACACTGAA | 55819 |
| rs540804603 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926102 | AGGCTAGGCAACTTA[C/G]GGTCTGGTAGGGGTT | 55819 |
| rs540808681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992163 | GCTTTTTGTTTTGAG[A/G]TGGAGTCTTGCTCTT | 55819 |
| rs540837240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942065 | GTTTCTTCACATCAT[A/G]CCAATAAATATTCCA | 55819 |
| rs540859842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179985122 | CTTGAATTTCTTCAA[C/T]ATCCTCATCTTGAAA | 55819 |
| rs540874967 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037200 | AATCTGCTGTTACAA[C/T]GCTGTAACACTCTCC | 55819 |
| rs540900176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951308 | GAGAAGAAAAACAAG[A/G]TAAGATTTGAGCAAC | 55819 |
| rs540908217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037366 | GCAAACAGCAGTTGT[A/G]CTCCACCGTAGGCAT | 55819 |
| rs540934779 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975145 | ATGAGGTACAGAAAG[A/C]CACAGCAGGTAACAC | 55819 |
| rs540988577 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179969190 | TAACCCTGGCTATAC[A/G]TGCTTCTCTTAAGCA | 55819 |
| rs541010030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179934110 | GACGACTTTGAAGCA[C/T]GGCCTAATAAGAACC | 55819 |
| rs541021547 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180025968 | TTTTCATAAAGTATT[C/T]TTTGTATTCACAGTG | 55819 |
| rs541026792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017079 | CATGCTTAGCTGTCA[C/T]GTCTCATTAGTCTCC | 55819 |
| rs541039317 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009965 | AACTTGAAAGTATCT[G/T]GGCCGGGCGCAGTGG | 55819 |
| rs541089049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018422 | TTCACAGGGCAGCAG[A/G]AGAGAGAACGAGTGC | 55819 |
| rs541093307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975044 | GTGCCGAATGCGGAG[C/T]GCCAGCCAGGCGGGG | 55819 |
| rs541132505 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179957626 | AGAGGTGCTGGGTTT[G/T]AATTCCAGTGGCCTT | 55819 |
| rs541158885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970095 | AGGAGTTCGAGGTTA[C/T]AGTAAGCTATGATTG | 55819 |
| rs541164531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055759 | AGCTGATACTTCTCT[C/T]TTTTTAGCTACTATA | 55819 |
| rs541194526 | snp | C/T | 0.000190188 | 0.00974977 | intron-variant | RNF130 | GRCh38.p7 | 5:180040671 | AAAAAGAAATACACA[C/T]ATTAAAGATAAATAA | 55819 |
| rs541223471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011134 | CGAAGGAACACAACA[C/T]GTCGGATAAACTCAA | 55819 |
| rs541234838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951365 | TACAGAACAGTCCAT[C/T]CAACAAGAGCAGAAT | 55819 |
| rs541297835 | in-del | -/TTTTTCTTCTCATTTTATT | 0.00874735 | 0.0655527 | intron-variant | RNF130 | GRCh38.p7 | 5:179940885 | ATGCCTTTTTCTGTA[-/TTTTTCTTCTCATTTTATT]TTTTTGCTTCAGCTC | 55819 |
| rs541298528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004725 | GGTTCAGAGTATATT[A/G]AGGATAGGTCACTTT | 55819 |
| rs541342301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965400 | TTTTATTTATTAACA[A/T]CATGTGCAAATTCTG | 55819 |
| rs541343304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945336 | CTGCACAGATCAGCT[G/T]CAAAACCTCAGCGGC | 55819 |
| rs541379419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033552 | AACATGGTGAAACCA[C/T]GGTGGTGTGCGCCTA | 55819 |
| rs541436891 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179939656 | GAGAATGAAGTGAGG[A/C]CCTGTGACCTAGTGA | 55819 |
| rs541476962 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005248 | GCCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 55819 |
| rs541481090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030291 | TTGAGGACATACAAC[C/T]GAAACCTGTTTCAGT | 55819 |
| rs541509198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180068391 | TTTCTAAACACGAAT[C/T]CTTTACCAGTTAAAA | 55819 |
| rs541521521 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982973 | TACATTGTCTGTGGT[A/G]AAGTGTCTGTTCATG | 55819 |
| rs541577581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930951 | GGAGGCTGAGGCATG[A/C]GAACCCAGGAGGCAG | 55819 |
| rs541590902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179924643 | AAAATATAAAAATTA[A/G]CCAGGCATGGTGGCG | 55819 |
| rs541591670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022425 | TAAGACCCTGTGTAC[A/G]GAGCTTTCCTAACTT | 55819 |
| rs541630193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015344 | AACTGAGACGGATCC[C/T]ACAAACGACATATGA | 55819 |
| rs541633518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180007448 | AAATCAGAGTCTGTC[C/T]TTAAACTCACTGGTT | 55819 |
| rs541645315 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938126 | CACGTCTGGCTAATT[C/T]TTGTATTTTTTTGTA | 55819 |
| rs541663114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062041 | GGCAAACATGCTTCC[C/T]CCTCCCCCAGCCTCT | 55819 |
| rs541691587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008296 | CTACTCCAGCCAGGC[A/G]CCAAGGGCAAAATCA | 55819 |
| rs541723114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958985 | CACGCCAGGCCACAA[A/C]GTTCTTTCTTATATC | 55819 |
| rs541765914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029564 | AACAAAATGGCATTT[A/T]TACTAATCTTAAAAA | 55819 |
| rs541772950 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032827 | TTCCATATAATTTTA[A/G]GATCGGCTTATCAAT | 55819 |
| rs541784584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959556 | TTCTTGAACCCGGGA[G/T]GTGGAGGTTGTGGTG | 55819 |
| rs541789986 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180045992 | GATGGGACCGAGCCC[A/C]GTGGAGCAGGGGGCA | 55819 |
| rs541807062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941912 | ATTTAAAAAATGAAA[C/T]AGAGAAGTACATTCT | 55819 |
| rs541824806 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033658 | CCAAGGTCGTACCAC[C/T]GCACTCCAGCCTGGG | 55819 |
| rs541830085 | in-del | -/A | 0.488606 | 0.0746142 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015737 | TAGGAAAGGAGTAGG[-/A]AAAGGAGTAGGAAAG | 55819 |
| rs541842246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001038 | TGGACAAAGATTTTC[A/G]CCTACAGTTTAATCT | 55819 |
| rs541846248 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956818 | AGCCCTGAGCTCTGG[C/T]GGGGCCAGACCAGGT | 55819 |
| rs541848113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933931 | GAGCAGACTGTTCTG[C/T]CATTTTTTCTAGATC | 55819 |
| rs541854296 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | RNF130 | GRCh38.p7 | 5:180071220 | CGAGCTGCCTGAACG[A/C/T]AAAGATGACCGTTCC | 55819 |
| rs541868662 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942541 | GCCCAGCTGAGCCTT[C/G]AAACTGCAACCTTGA | 55819 |
| rs541895845 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980611 | ATCACCATTAGGTGT[C/G]TAAATGCCGTCTTAT | 55819 |
| rs541905623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993793 | TTTTAGACATGAAGT[C/T]CTTGCCCATGCCTAT | 55819 |
| rs541959249 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002566 | TCAGCTGGGCTTAGT[A/G]CCTGTGAGGACTGGT | 55819 |
| rs541963607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039263 | TTTTTTTTTTGAGAT[G/T]GAGTCTTGCTCTGTC | 55819 |
| rs541979015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065029 | CCTCTTTTCTTACTA[G/T]AGAAAAAACACGCCT | 55819 |
| rs541981737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944129 | GGTGCCTGCCACCAT[A/G]CCTAGCTTTTTGTAT | 55819 |
| rs541986787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179934689 | GCCAGACCACAGGTG[C/T]GCGCCACCACATCCG | 55819 |
| rs542011552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179967872 | AGTGTACTAAGTGAT[A/G]CTTAGGCTCACACCC | 55819 |
| rs542012360 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054018 | GATGGGGTTTCACTA[C/T]GTTGGCCAGGATGGG | 55819 |
| rs542020632 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936758 | AGGCAGCATGGTACT[A/G/T]CCATAAACACAGACA | 55819 |
| rs542027519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058764 | ATGGGGTTTCACCAT[A/G]TTAGCCAGGCTGGTC | 55819 |
| rs542063925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179921760 | CAAGATCGCGCCACA[C/T]GCCTGTCATCCCAGC | 55819 |
| rs542069216 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073053 | AACTTACAGGATCTT[C/T]GTGGGGAGGCGGAGG | 55819 |
| rs542079301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024156 | TCATCAAAAACAAGG[A/G]AAGTCTAAAAAAGTA | 55819 |
| rs542086773 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036700 | TCACTTCGTCTTAAC[C/T]GGAAGTGCTACCCCT | 55819 |
| rs542149189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067100 | GGAGGGATCTCAGAA[A/G]TTATCTAGTCTTGAG | 55819 |
| rs542154768 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986428 | ATACAGGTCCCATGG[C/T]GTAATATTCAAGATT | 55819 |
| rs542196552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179929330 | GTCCATCCTTGCATC[A/G]ATACCTTACTGTCTT | 55819 |
| rs542267512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994322 | TGGCCATTTTCACAA[C/T]ATTGATTCTTCCTAT | 55819 |
| rs542281217 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180049618 | TACATTGTTTCAGTA[C/T]ACTTGGGTTTCTTTA | 55819 |
| rs542283899 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953814 | CACTACCAAGAAAGT[A/G]AATAAATAGTTTAGA | 55819 |
| rs542297174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986590 | GCAACACTGGTGATC[A/G]CAATAGCAACAGGTG | 55819 |
| rs542324095 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968660 | GACAAAGGGAGACTC[C/T]GTCTCATAAAAAAAA | 55819 |
| rs542325337 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179997518 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 55819 |
| rs542355387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031395 | GGGAAGCTGAGGCAG[G/T]AGAATTGCTTGAACC | 55819 |
| rs542360363 | in-del | -/CCTGC | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:180064416 | GCCCCAGTCACCCTA[-/CCTGC]CCATAGTCCCCAGAG | 55819 |
| rs542361150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042913 | GATCAACTGCTTACT[A/T]GCTGTGTAACTATCA | 55819 |
| rs542371482 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179946584 | TTTGAGACGGAGTCT[C/G]GCTCTGTCGCCCAGG | 55819 |
| rs542376281 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179982307 | GTTGATGGGACATCT[G/T]CACTGTGGTCCAGTT | 55819 |
| rs542379343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179939769 | CCCTCCCTTGGCGAC[C/T]CCTTTGATTCCCAAA | 55819 |
| rs542403093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034270 | TATATATTACTAGAT[G/T]CTATTTGCTAATAAT | 55819 |
| rs542406019 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044903 | CAGAAGCTGACGTTA[G/T]AGGGTGCCAACACGA | 55819 |
| rs542469969 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933671 | AGACCACAGTCACGC[C/T]CCACCATGCCGGGCT | 55819 |
| rs542481818 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922905 | CACTACTGCCCTCCA[A/G]CCTGTGCTACAGAAA | 55819 |
| rs542485501 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064294 | GAAAAAATAAAAATA[A/G]GGAGCAGATTCATTT | 55819 |
| rs542504145 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180069272 | TTTGTTCACTGCTGT[A/T]GCCTCTCCTTCACCA | 55819 |
| rs542512977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974563 | TGACAGCTCTGGATA[C/G]AAAGTCCTAGCTGAG | 55819 |
| rs542532989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971493 | TCCTGCCTTAGCCTC[A/C]CAAGCAGCTGGGACT | 55819 |
| rs542541662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024780 | GCCTACCGTTTTTTC[A/C]TGAGTTTTGCCATTC | 55819 |
| rs542542806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062264 | ATGGGGTTTCACCAT[A/G]TTGGTCAGGATGGTC | 55819 |
| rs542576463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016267 | ACCCCTAAAGCCTGA[C/T]AGGGCTCAAAGACCC | 55819 |
| rs542577161 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179976715 | TTTTTTTTAAAAACA[A/G]ATCTTCCTAGACTCA | 55819 |
| rs542593415 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028486 | TTTCTCTTTCTGGTC[A/G]AATCCTAAGTAATCC | 55819 |
| rs542723338 | snp | A/C/G | 0.00398731 | 0.0445001 | intron-variant | RNF130 | GRCh38.p7 | 5:179960479 | CTTGGTCAATGCACC[A/C/G]AGCGTGGTGAGGAAG | 55819 |
| rs542831938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027761 | ACTCCCACCCAATGC[C/T]TCCTGCTGGTTTTCC | 55819 |
| rs542836938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180006373 | AACCTTTCTCTGACA[C/T]AGGAATGTTCCATAT | 55819 |
| rs542870545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991999 | GATCTGAGAGGAGGA[A/G]CAGCTCAGGAAGTAA | 55819 |
| rs542938996 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179954458 | ACATGCTAAGTCAAA[A/G]ACGCCAGACACAAAA | 55819 |
| rs542948810 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179931797 | ACAAACAACAAAACT[A/G]CAGTACAAAGACTTT | 55819 |
| rs542998225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947454 | CAGGACACCCCACAG[C/G]CTGCCCCTGACACTT | 55819 |
| rs543037493 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036114 | GTTGAAAAGTGAACA[C/T]TTTAGACAGTATATT | 55819 |
| rs543040004 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990461 | GAGCGGACCAGGGGC[A/G]TGACCGCTGAAGCAC | 55819 |
| rs543043503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020917 | CAAATTACTGATCCT[C/T]TCAACTGAGTAGTTC | 55819 |
| rs543046306 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968323 | ACAAACAAAAAAAGA[A/C]GGCGGCGGCTAGCGG | 55819 |
| rs543050894 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179994765 | AGTGCTGTGCACTTA[C/T]GTAAGCAGATGTTGT | 55819 |
| rs543063381 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180057571 | AAAATCATGTGTAAT[C/G]TGTAATGGAGCCTCC | 55819 |
| rs543063730 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180066305 | ATTTTCTCTTGCTGC[A/C]GCCATGTAAGAAGTA | 55819 |
| rs543077286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005465 | CCAACAGAAACCATA[C/T]TGATTATAGAATAAA | 55819 |
| rs543113597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968736 | TGGCAGATGCTCTAT[C/G]TTAGACCAGTCTGAA | 55819 |
| rs543126207 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989173 | AGACGCTTATAAAAC[A/T]ATCCCATCAGATCTT | 55819 |
| rs543150050 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012643 | TTCATTTTCTGAATA[C/G]ATAATACTTTCCCAG | 55819 |
| rs543156608 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940160 | CTTAACAGACGGTTG[A/G]AATGGGCAAGGGTGC | 55819 |
| rs543178657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953831 | ATAAATAGTTTAGAG[A/G]ATGTGAGAAAATATT | 55819 |
| rs543182215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009337 | CTGGGAGATAATCTC[C/T]GCAAGCCACATATTT | 55819 |
| rs543190722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998725 | TGTTACTTCCATTTG[A/G]TCTAAAGTGCAGTTT | 55819 |
| rs543223020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956797 | TCAGTACGCACATGA[C/G]GGCATAGCCCTGAGC | 55819 |
| rs543258984 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999833 | TTTTAAGTGGTGAAA[C/T]TTAATCTGCTTACAT | 55819 |
| rs543262646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179921592 | CATTTGAGATCAGGA[A/G]TTCAAGACCAGCTTC | 55819 |
| rs543280791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995308 | TTTGCTATTGGGTCC[A/C]AAACCACACCTCTCA | 55819 |
| rs543317249 | in-del | -/TTC | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179946507 | ACAAATGTACTAGCG[-/TTC]TTCTTAGTCTTAACA | 55819 |
| rs543371234 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038225 | ACACCTGCTAATTTT[C/T]GTATTTTTTTGTAGA | 55819 |
| rs543387988 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179936666 | AAAGTAAAGCATCTC[G/T]TTATTGAAAAAGGAA | 55819 |
| rs543389612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036447 | GAAACTGCCAGTCCT[C/T]GCAGCCTGCTCCACA | 55819 |
| rs543394372 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968483 | CCAGCCTGGCCAACA[A/T]GGGGAAACCCCATCT | 55819 |
| rs543395667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024024 | CTTTACAAATCCCTG[C/T]GGTCTTCCTCCCAAA | 55819 |
| rs543425050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929206 | GTGGAGCCAGCACCA[C/T]CTTGAAAAGACCATT | 55819 |
| rs543436207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025106 | CTGTAAGCATCAATG[C/T]GGGGTAGAGATCCTC | 55819 |
| rs543438768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015445 | GAAGACTCAAGCTGG[A/G]AAAGGAGTAGGGAAA | 55819 |
| rs543441922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057303 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 55819 |
| rs543456752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988891 | TGTAAATGTCTGTTA[C/T]GTCCATTTGGTATAT | 55819 |
| rs543501075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922458 | GCTGAGATTACAGGC[A/G]TGGGCCACAATGCCC | 55819 |
| rs543560744 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010414 | ACCCAGGCTGGAGTG[C/T]AGTGGTACGATCATG | 55819 |
| rs543573546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963740 | TGGAGAAGGTTAGTG[A/G]AAGTACTGGTGAAAG | 55819 |
| rs543582868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180054042 | GGATGGGCTCCATCT[C/T]TTGACCTCGTGATCT | 55819 |
| rs543608562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002381 | CTGGGGTGGTTTGGT[G/T]GCAGCTTAGCCTTAG | 55819 |
| rs543615412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046225 | GCAGGTGCAGGGCCC[A/G]CCAAGCTCACACCCA | 55819 |
| rs543617828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019133 | CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 55819 |
| rs543662671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924524 | AAATACAGGCTGGGC[A/G]CAGTGGCTCATGCCT | 55819 |
| rs543683557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179957526 | TTTAGGAAACCAAAT[C/T]TGTCTCCTTCAACCA | 55819 |
| rs543703546 | snp | A/G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943773 | AGCTATGATTAAACC[A/G/T]CAAAGTATATTTAAC | 55819 |
| rs543705860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046743 | ATGTCTTCTCCAGAA[C/T]GCTTTCCCAGCCTCC | 55819 |
| rs543711137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055857 | GGGAGGCTGAGGTGG[A/G]TGGATCATCTGAGGT | 55819 |
| rs543724385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950036 | TCCAGCTCTGTGCTT[A/G]AGCAAACTCTATACT | 55819 |
| rs543729937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003446 | TGAACTTTGAACACC[C/T]CTTATAGCACAAGGA | 55819 |
| rs543771925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958341 | TGTGTGAAATTTGTT[A/T]CAGTTACACATGGGA | 55819 |
| rs543783668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991282 | ATGACTATATGTCAT[C/G]GTGAAGTCTTTAAGC | 55819 |
| rs543785383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950664 | TCAATTCACTCATTT[C/T]GCTTCTTAGCTCTTA | 55819 |
| rs543786162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180034155 | TTTTTCTGCACCTAC[C/T]GAAAATGGTTAGTTG | 55819 |
| rs543801027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041165 | TTGAAATTCAACCAT[A/G]TTAGAGCAAATTTCT | 55819 |
| rs543824368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033530 | GGAGTTCGAGACCAG[A/C]CCGGCCAACATGGTG | 55819 |
| rs543834059 | in-del | -/AA | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180054824 | GGACCTATGAACATG[-/AA]AAGTCTGTTTATTTA | 55819 |
| rs543844475 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179991956 | CACAGTAGGCTTCAC[A/C]CTCCTATGAGAACCT | 55819 |
| rs543856930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179981357 | GGAAAAGGCAGATGC[C/T]GCTCCTGACGGAGCA | 55819 |
| rs543857262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945294 | GACTGCACCTGGGAA[A/G]ACAGTGGGACCCAAT | 55819 |
| rs543860940 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937820 | TCAGTGGATGAGGAG[A/C]TGAACAAATTGTGGT | 55819 |
| rs543880474 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180028752 | TGCCTGGCATATAGC[A/G]GGTATAAATCGATAC | 55819 |
| rs543881716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180032027 | TAAAATGTCTAATTA[C/T]TAAACCTTTTGCCCG | 55819 |
| rs543915591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975029 | CCTGCAGGTGCTGCT[A/G]TGCCGAATGCGGAGC | 55819 |
| rs543933240 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179984597 | TTCCTGGAGTAAACA[C/T]CACCTGGTCATGATG | 55819 |
| rs543937414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925913 | GTGCCTCAAAGGAGG[C/T]TGCATGAGGCACAGT | 55819 |
| rs543938877 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179938807 | TCTGTAGAAGACTCA[A/C]CCTGGCAATGTTAAC | 55819 |
| rs543942311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029343 | TTTCTAAGGTGATGA[A/G]TATGTGACAGGCAGC | 55819 |
| rs543947703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180036221 | GTAACAGGCTGGGTT[A/G]AACACATGAAATCTA | 55819 |
| rs543954454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021732 | CCTGGCATGATGCCT[C/G]ATCACCCCCGAATAT | 55819 |
| rs543963265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067929 | AACCATTAAAGGCTT[C/T]GTCTAATAGGATTAC | 55819 |
| rs543996733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977604 | ACGCCTGTAATCCCA[A/G]GACTTTGGGAGGCTG | 55819 |
| rs544000240 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001394 | AGAGTCTCACAAATG[C/T]ATTTGTGGCACCTGT | 55819 |
| rs544005807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179941778 | TTCTTCTTGATATGA[C/T]GGTTGCACCACAACA | 55819 |
| rs544016444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022315 | TACTTTTACTTTTTA[A/G]ATCAGTACAGATTCA | 55819 |
| rs544020956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926827 | CAGTCTTGTGGGACT[A/G]AGCCCTCACCCTGGG | 55819 |
| rs544027249 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179950081 | GAATCTCATTATTTA[A/C]GGTTGACAGTTGATA | 55819 |
| rs544049854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180061343 | TAGCTCGACTCTCTC[C/T]TGTGCTGGCAAAGCT | 55819 |
| rs544059236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933839 | ATTTTCCCTCCTGTG[C/T]GTTTTTGTCTTGCTT | 55819 |
| rs544061427 | snp | A/G | 0.000372856 | 0.0136488 | intron-variant | RNF130 | GRCh38.p7 | 5:179920435 | TGACCACCTGGAAAA[A/G]GAAGAAGAGAAAGAG | 55819 |
| rs544061442 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927537 | ATGTCCTCTCTCCCC[C/G]GCCAAAGGAAACCAT | 55819 |
| rs544062619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970055 | CAGCTACTCAGAAGG[C/T]GAGGTGGGAGGACTG | 55819 |
| rs544111359 | in-del | -/ACA | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179952927 | TTTCCCTACGAGATC[-/ACA]ACAACACATGGATGT | 55819 |
| rs544126990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179964514 | CAATAAAATTACCTA[C/T]ATATGTGCAAGAAGG | 55819 |
| rs544130332 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064698 | CCTGTGAGATGAATA[A/C]ACTGACTCCCTCGCC | 55819 |
| rs544136993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056510 | GTCTAAAGAGGGAAA[C/T]GCCTCAGTTTCTGGC | 55819 |
| rs544140461 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF130 | GRCh38.p7 | 5:180053921 | TGCAACCTCTGCCTC[C/T]CAGGTTCAAGCGATT | 55819 |
| rs544173154 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | RNF130 | GRCh38.p7 | 5:179927753 | ACCACGCCTGGCTAA[-/T]TTTTTTTTTTGTATT | 55819 |
| rs544182416 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179946749 | TTAGTAGAGACGGGG[C/T]TTCACCGTGTTAGCC | 55819 |
| rs544185163 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046864 | TGTTTACTTCTGAGG[C/G]TTTCCTTCCGGAATG | 55819 |
| rs544243076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984014 | TCAGCCTCACAAGTA[A/G]CTGGAACTACAGGTG | 55819 |
| rs544244186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947206 | TTAAACTAGCAATTC[C/T]ATCTTTAGTAACCCC | 55819 |
| rs544247079 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972930 | TCTGTTTTACTAAAC[-/A]AATTAAAAATTTCTC | 55819 |
| rs544273329 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180007355 | GCAGTGAGCCAAGAT[C/T]GCGCCACTGCACTCC | 55819 |
| rs544340766 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923657 | CCAGCTGGTTCTGTA[C/T]CTCACTTCCCTTTCC | 55819 |
| rs544348464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180045849 | GACACAGAGTGCTGA[C/T]TGGTGCATTTACAAT | 55819 |
| rs544356625 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942756 | TCTGGACTTCAAATA[G/T]GTGATGTTTTCTTCA | 55819 |
| rs544356673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948763 | AGTCAAGGAAGCTTC[A/G]GGATCTTTTACCAAT | 55819 |
| rs544407788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063836 | GAAATTTTGTGTTTA[C/T]AAAAGACTTCTGTAA | 55819 |
| rs544421419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943180 | AGCCTGGGACAGAGC[A/G]AGACACTGTCTCAAA | 55819 |
| rs544433989 | snp | C/G | 0.00716266 | 0.059414 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071822 | CTGCGCGGGGCCGAG[C/G]CCGAGCGCGGCCCTC | 55819 |
| rs544441242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038380 | AGTTAGACCCTGTCT[C/T]GGGGAGGGGGAAAAA | 55819 |
| rs544447881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058131 | GTGTCAAAGCGAGGA[C/T]AGAAGTTACTGCTGG | 55819 |
| rs544496224 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072691 | GCAGTTCACAGCCGG[C/G]TTCACGTTGCTATGA | 55819 |
| rs544503059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961309 | TCCTTCGGTGGTTTT[C/G]ACTGAAGGCACAGAA | 55819 |
| rs544519491 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180020876 | TCCAGGGGTTGCCAA[A/C]TTTCAACACAACACA | 55819 |
| rs544523378 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022286 | AATATTCCATCCTCA[C/T]GAAACCTTCAGTTTA | 55819 |
| rs544523505 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180006632 | GTCCATTAAGTGGCA[C/G]AATATTTTACATCTG | 55819 |
| rs544524397 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179973992 | CCCTTTCCTATGTCC[C/T]ACACATGCCATGAAC | 55819 |
| rs544527255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179973377 | TGCTAGTCTCTTCAG[C/T]GCAACTTTCACTGAA | 55819 |
| rs544537263 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179979222 | ATTGAAATGCAAGCC[A/G]TTTTGATGCTGCTTC | 55819 |
| rs544616095 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993040 | TCATCCATGTCCCTA[A/C]AAAGGACATGAACAC | 55819 |
| rs544620354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000274 | TGGAAAAATCTGTTT[G/T]TAGTCTAATAGGGAT | 55819 |
| rs544654606 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179952185 | CCTGGGTGACAGAGC[A/C/G]AGACATCTCAAAAAC | 55819 |
| rs544673604 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948661 | GGATGATAGATAGAG[C/T]GAGACTCTGTCTCAA | 55819 |
| rs544682094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958173 | TGAGCCACCGCGCCC[A/G]GCCAAATTCAAAATT | 55819 |
| rs544683701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179992967 | CCTATGAGTGAGAAC[A/G]TGTGGTGTTTGGTTT | 55819 |
| rs544742142 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180037449 | GCCTCTATCCTCCAA[C/T]CCGCACTCAGGAGGC | 55819 |
| rs544745881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958773 | CTCACTGCAACCTTC[C/G]CCTCCCAGGTTCAAG | 55819 |
| rs544753825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048406 | GATTAACCTCCGAAT[C/T]TAGGCAATTTCTGCT | 55819 |
| rs544758024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179951973 | ACCTCAAATCAATAA[C/T]CTCATCTTCCACCTT | 55819 |
| rs544775548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986083 | AAGTTGTCATATAAT[A/G]ACTTTTCTTTTCCTC | 55819 |
| rs544777561 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948798 | TTTAAAGTCTAAAGT[C/G]ACAACCTAGCTAGCC | 55819 |
| rs544806257 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974842 | GCAGGCACGCAGCGG[C/T]GCGGGGAGGAGCGGC | 55819 |
| rs544894581 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973787 | AATAAAAAACAGGCC[C/T]GCCACACACAGGGTG | 55819 |
| rs544911530 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971616 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 55819 |
| rs544912090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979952 | CAGAAGAAACCTCTG[C/T]AGGAAAACACAGCTA | 55819 |
| rs544933401 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995596 | CAGGTCTGGGAAAAT[A/G]CATGGGATGCATCCC | 55819 |
| rs544943327 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925578 | GTTGCCCAAGCTGGA[C/G]TGTGCAGTGGTGCGA | 55819 |
| rs544955915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023275 | GATACACGCATGTAT[C/T]TCCTTGTTCTGTCAG | 55819 |
| rs544956707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964498 | TTAACAAAATGTTAT[A/G]CAATAAAATTACCTA | 55819 |
| rs544979163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010353 | TATGATTCCACCTAT[A/G]TAACATTTTTTTCTT | 55819 |
| rs544999142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982900 | CCTTACAGTTTTAAT[C/T]TGCATTTCCCTATTG | 55819 |
| rs545065744 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940303 | TCGGCTCACTGCAAC[C/T]TCCGCTTCCCAGGTT | 55819 |
| rs545080915 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063445 | ATGGGAAAGACTGGA[A/G]AGCAGTGGTAGCAGA | 55819 |
| rs545087732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003813 | ACCTTCACCTAAACA[A/C]CATGCCATTAAGTCA | 55819 |
| rs545136629 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008632 | GCTCATGTCTGTAAT[C/T]CCAGCACTTTGGGAG | 55819 |
| rs545153920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041925 | ACAAAAAAATTAGCT[A/G]GGTGTGGTGGGGCAC | 55819 |
| rs545177284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949047 | CTCAGCTCACTGCAA[C/T]CTCTGCCTCCCGGGT | 55819 |
| rs545187731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033628 | TTGAACCCAGGAGGC[A/C]GAGATTGCAGTGAGC | 55819 |
| rs545189562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004918 | CCTTCATTCATTCAC[C/T]ACCATTTTTTCCCAT | 55819 |
| rs545202019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996754 | TTTATGTTCATCAAG[A/G]ATACTTGTCTATATT | 55819 |
| rs545205162 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179945969 | CCTATCACTCCCCAC[A/G]GCCGCATCTGCCCAG | 55819 |
| rs545210973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063038 | ACCTGGGGGTGGGGA[A/G]GAGGAAGGGGCTGGA | 55819 |
| rs545227676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989911 | TTTATACTTTCATGT[A/G]TTTTTATGATGGCAA | 55819 |
| rs545234428 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924228 | CTGCTGGGCGTGGTG[A/G]CTCACGCCTGTAATC | 55819 |
| rs545243699 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179966282 | ACCTCATGTACAACT[A/G]CACCAAAGAGTTAAG | 55819 |
| rs545250215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179982135 | GAGTTTTACATAAAT[A/G]GAATAGATACAGTAT | 55819 |
| rs545262686 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045523 | CCCACAGCGCGGAAG[C/T]GGACCTCTGCACGTT | 55819 |
| rs545263956 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994999 | AGAGGTGAAGCTGGG[C/T]AGAGCTGGACTGGGC | 55819 |
| rs545274088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005383 | CAGTGAGCTGTTAAT[C/T]GAGCCACTGTACTCC | 55819 |
| rs545275787 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179978078 | CCAGCAATGCACAGC[C/G]GACTTGGCCTCCAGA | 55819 |
| rs545302217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034182 | GTTGGCTTTTTCATT[C/T]ATTCTATTGATTTTC | 55819 |
| rs545332370 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179939722 | TCCACTTCCAAAAGA[C/T]GGAAATCCACTGAAA | 55819 |
| rs545400855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069236 | GCTATGCTTCATAGA[C/G]ACGGATTTTTTTAAA | 55819 |
| rs545416707 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180042149 | ACATGCCTAGCAAAA[A/C/G]AAACTAAATGCTTAC | 55819 |
| rs545417045 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014102 | ACCTCCAGCCTCTAA[C/G]AGTTGTCCAGAGGTC | 55819 |
| rs545422135 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179973604 | CGGGCAGAGCGGCCC[C/T]GCCACCTGGCCATTC | 55819 |
| rs545439969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931633 | AATTAGCCGGGCGTG[A/G]TGGTGCCTGCCTGTA | 55819 |
| rs545459087 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061219 | GCTTAGGAGCAGCCT[C/T]GGTGGAAAACACTGG | 55819 |
| rs545484230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973940 | CAAATAGAACATGAA[A/G]GGAACAAACCCAGCA | 55819 |
| rs545492126 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072589 | GGACTGAGGGAGTTG[A/G]AGTGGTTTCCGGATG | 55819 |
| rs545493692 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179965680 | ACCATGAAATGCTAT[C/T]AAACGAATCGAGAGA | 55819 |
| rs545537712 | in-del | -/TGCCT | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179948853 | TTATCAGGCTAAGAC[-/TGCCT]TAAGCTGCTGGGTAG | 55819 |
| rs545553269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051344 | AAGCTCTGCCTCCCG[A/G]GTTGACGCCATTCTC | 55819 |
| rs545554960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179959817 | CCTGATCTCCGGTCA[C/T]GCCACTGGATCATTT | 55819 |
| rs545577876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180065727 | ATCATGCCACTGCAT[C/T]CTAGCCTGGGCGACA | 55819 |
| rs545584273 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180008531 | AGAAGAGAACTGAAA[C/T]CATAGAGTATTTCTC | 55819 |
| rs545596684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009076 | GAAATTTATAGCACT[G/T]AATTCTTACATTAGA | 55819 |
| rs545606649 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015438 | CCCTCTTGAAGACTC[A/G]AGCTGGAAAAGGAGT | 55819 |
| rs545612109 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992874 | TGCTATCCCTCCCTC[C/T]TCCCCCCAACCCATG | 55819 |
| rs545641962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057526 | GCGCTCCAGCCTGGG[C/T]GACAGAGCGAAACTC | 55819 |
| rs545647323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962696 | ACTCTTGGAACAGCA[C/T]TGGATCAAAATGGAC | 55819 |
| rs545656016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001863 | CTAGTACAGGTTCAA[A/G]CAAGCAGGGTACTAG | 55819 |
| rs545662505 | in-del | -/CACG | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179946708 | ACAGGCGCCCGCCAC[-/CACG]CCCGGCTAATTTTTT | 55819 |
| rs545669930 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960531 | GTGGGGATCCTCCTT[A/G]TGTAGTTAGCAACCC | 55819 |
| rs545677783 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:179921938 | AGGCAGGAGAATCAC[C/T]TGAACCCAGGAGGCG | 55819 |
| rs545678987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050667 | AGAAGTTCTTTCAAT[A/G]AGGATCTGTTAGGTA | 55819 |
| rs545699438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952926 | TTTTCCCTACGAGAT[C/T]ACAACAACACATGGA | 55819 |
| rs545706333 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983710 | TGAGATTGTGCTGAA[C/T]GTATACATCCACTTG | 55819 |
| rs545738808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022534 | GAGTAGCATGACACT[A/G]ACATCTCCTTACATC | 55819 |
| rs545750513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016086 | AGCACAGAGAAGAGC[C/T]GGGCAGAGGAGCCCG | 55819 |
| rs545757063 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072162 | CCCCCCCGCTGGTCT[A/T]GCGGCAACGCGCAGG | 55819 |
| rs545758564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953751 | CAACCAAAGGAAAAA[C/T]AAACATATTCAACTT | 55819 |
| rs545772824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031127 | CAGCATATAACATAT[A/G]TAACAAAGTATGTAT | 55819 |
| rs545783693 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031089 | CTTCCTTATGATTTC[C/T]TTAATAACATTTTCT | 55819 |
| rs545793746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065052 | ACACGCCTTTTTCAA[C/T]ATTTTCCTAGTATCC | 55819 |
| rs545801549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934793 | TGTGATCCTCCATGC[A/C]TCAGCCTCCCGGGTC | 55819 |
| rs545836103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927735 | GGGACTACAGGTGCC[C/T]GCCACCACGCCTGGC | 55819 |
| rs545837776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935659 | TCCTATAGTCCTCTC[C/T]TCTAAGTTTTTTCCT | 55819 |
| rs545846836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921127 | TTTACTGGGGTATAA[A/C]TGACATACAATGAAA | 55819 |
| rs545867852 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977451 | AAACAATGCCAAGCA[C/T]AGTGACTCATGCCTG | 55819 |
| rs545868989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031943 | TTTTAATTATGATCA[C/T]TCTAGAGGATGTGAA | 55819 |
| rs545873532 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179967952 | ACCTGCAATACATTT[C/T]AGGAGGATTTTTGTT | 55819 |
| rs545874591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928481 | CAGGCTGTTTGTGTA[C/T]CTGGTTCGCTCTGAA | 55819 |
| rs545894392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179944159 | TTTTTAGTAGAGACG[A/G]GGGGGTTCACCATAT | 55819 |
| rs545927187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179987340 | ACCTGGCTAATTTCT[A/G]TATTTCTTGTGGAGA | 55819 |
| rs545930534 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180024226 | TGTAATGTGGTGTCC[A/T]GGGTGGGATCCTAGA | 55819 |
| rs545932394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032615 | CCCTCACTGAATGAT[A/C]GTGGCACTTTTGTTG | 55819 |
| rs546009698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986111 | CTCAAATCACATTGG[A/G]TACTACAGGTATGCC | 55819 |
| rs546010564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930058 | CATTTTATTTATTTA[C/T]CTTTTATTTATTTTT | 55819 |
| rs546027392 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179936987 | ACCTAAATGTGAGTT[C/T]TAAAAGTATAAAACC | 55819 |
| rs546042632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993977 | GCGTCATTTCTTAAA[C/T]AGGGAATCCTTTCCC | 55819 |
| rs546052062 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073707 | TTTACTTATCCTCGG[C/T]AAGTACAGACCCTAG | 55819 |
| rs546057578 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980812 | GGCAGAGAAACTCCA[A/C/G]GGCTGGATTTATGCA | 55819 |
| rs546061125 | snp | A/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072754 | GGAGCTCAGGCGGTG[A/T]TGCTCACTCACCTCC | 55819 |
| rs546067563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180046033 | GGGAGGCTCCAGTGG[C/T]GTGGACGGAGGGGGG | 55819 |
| rs546086305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180060315 | ACCAAGGCTAAGCCA[C/T]GAAAGATTCACTTCT | 55819 |
| rs546091214 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067205 | ACAGGTAGCTAAGCC[G/T]TAGCTCCCTTCTGCT | 55819 |
| rs546096357 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022333 | CAGTACAGATTCATG[G/T]TTCCTATTTTATTCA | 55819 |
| rs546100879 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | RNF130 | GRCh38.p7 | 5:179956014 | GGTGCTGAAATCTGC[A/C/T]GCTGTTGTCTTTAAA | 55819 |
| rs546123080 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180060840 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 55819 |
| rs546124985 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF130 | GRCh38.p7 | 5:180055469 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCGCACGCG | 55819 |
| rs546127301 | in-del | -/AAAAT | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180044840 | CCGTCTCAAAAAAAA[-/AAAAT]AAAAGCCTCCACATT | 55819 |
| rs546154446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034395 | GCTCCACAGAATAAG[C/T]TGAGAAATGTTCTCT | 55819 |
| rs546159864 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179949167 | ATGGGGTTTCGCCAT[A/G]TTGGCCAGGCTGATC | 55819 |
| rs546160546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939313 | GTGGTCCTAACAATA[A/G]ACTCAAAAGTTTATG | 55819 |
| rs546162067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956692 | AGTCACTCTTCCATG[A/C]AGCCTTTTCAGCTCC | 55819 |
| rs546169269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969284 | TCTGGCACGCCTGGC[A/G]ACAGCCCCTGCCAGG | 55819 |
| rs546174007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949847 | CTCAGATCACCACCC[C/G]TCCTCAAGGAGCAAT | 55819 |
| rs546181315 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953060 | GAAGAAAAATGATCT[C/T]TATGTACAGATGACA | 55819 |
| rs546197845 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953305 | CTATAAAATCCTAGC[-/T]TTTTTTTTTTTTTTA | 55819 |
| rs546216168 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995079 | AGGGATCTAGGGACA[C/G]TTGCCAAACCCTGTA | 55819 |
| rs546237251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179950505 | ATGCACATGTGCACA[C/T]AAAATATACCTTCAT | 55819 |
| rs546244988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180025753 | AGTACACTTCAATTC[C/T]AAGCTCCATCTTTTC | 55819 |
| rs546246147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026470 | GATCCGCTAACTACA[C/T]GACAAAGAACTCACT | 55819 |
| rs546256737 | snp | C/T | 1.69873e-05 | 0.00291434 | intron-variant | RNF130 | GRCh38.p7 | 5:180040429 | AGAAGAAAAACAAAA[C/T]CAACAACCCTCATTT | 55819 |
| rs546258069 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014788 | CTCAGGAGTCCAAGA[C/G]CAGCCTGGGCAACAT | 55819 |
| rs546264744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990060 | GTTTTTCTCCCCATG[C/T]GTGGAGACGAGAGAT | 55819 |
| rs546307825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944639 | GAATTTTGTAGAGAC[A/G]GTCCCCCAGTTCCTC | 55819 |
| rs546308343 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179992393 | GTGATCCACCCACCT[C/T]ATCCTCCCAAAGTGC | 55819 |
| rs546341911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974361 | TAAGAGGTCTAATAA[A/G]ACCAGGTGACAGTTC | 55819 |
| rs546361631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180061577 | GATGGCTGCTAGCCA[C/T]CCTTTGCACCCGCCG | 55819 |
| rs546369918 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015467 | GTAGGGAAAGGAGTA[-/G]GGAAAGGAGTAGGGA | 55819 |
| rs546380308 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179954461 | TGCTAAGTCAAAGAC[A/G]CCAGACACAAAAGGC | 55819 |
| rs546400712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180057074 | AATAAGCCCCTTTCA[A/G]CCATACCAGCGTCTG | 55819 |
| rs546402361 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180062353 | GTGTGAGCCACTGAG[C/T]CCGGTCCCCCCAGCC | 55819 |
| rs546417067 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952132 | GAGCCAGGGAGTTCA[A/G]GGCTGCAGCGAGCTG | 55819 |
| rs546446080 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974639 | ATCTCCCTCCCTCAC[A/G]GAGGGAAGAGGCAGT | 55819 |
| rs546452495 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180069472 | ACAGAATGACCCCTA[C/G]GGAATCAAGGAAAGG | 55819 |
| rs546473551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067902 | AAAAACCGATTTCAG[A/G]TTCATTAAAGGAACC | 55819 |
| rs546482113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959176 | TTCAATAAACAGTAG[C/T]TATTCTCATCTTTGT | 55819 |
| rs546482837 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928841 | CAACCGTGTTAGCCA[-/G]GATGGTCTCAATCTC | 55819 |
| rs546486606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057406 | ATACAAAAACTATCC[A/G]GGCATGGTGGTGCAT | 55819 |
| rs546494691 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960095 | TTTGAGGGAAAACTA[C/G]AGTGACACAAATTTC | 55819 |
| rs546501913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925610 | CCTAGCTCACTGCAG[C/T]GTCAACCTCCTGGGC | 55819 |
| rs546506433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180018167 | GGGTGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 55819 |
| rs546557955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953200 | TACAGAAATTAAACA[C/T]GTGGAACGATATCCC | 55819 |
| rs546595129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179981631 | AAAATTTTCACTAAG[C/T]ACCTCTAATAGACAC | 55819 |
| rs546627760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022718 | CACGTCTCCACAAAC[C/T]TTTGCTATACTAGTT | 55819 |
| rs546655684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027113 | GCTTCTGCCCTATGA[A/T]GAAGGGAGGGCAAAA | 55819 |
| rs546662260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983481 | ATGTGCGGACACTAT[C/T]GTACCATGCATCTAT | 55819 |
| rs546668475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953932 | CAATTTAAAAATGGG[C/T]AAAGCACCGGGATAG | 55819 |
| rs546668830 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179975700 | CTCAGCCAGGGCAGT[A/G]AGCACAGCTAGTAAC | 55819 |
| rs546690293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971013 | TAAAAGCTACAGGGA[A/T]GCTGAAACTATTTTA | 55819 |
| rs546717067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019629 | TCTCTTCACTGATCC[A/C]TTAAAGAACTCAAGG | 55819 |
| rs546741343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991561 | TTCTGTATTTCTGTG[C/T]GACCAGATTCATCCA | 55819 |
| rs546760806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925123 | GTGGTATCTTTCATA[C/T]GCTAAAGAGGTGGGT | 55819 |
| rs546768457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180011431 | ATTTAAGGGTAACAG[A/G]GCATCATATCTCAAA | 55819 |
| rs546769234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044140 | TAAAATATCTATATA[A/G]TTATGAGCCTTTAAA | 55819 |
| rs546778083 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179984276 | CTTTTACGTCTTTTC[C/T]TTTTTACTTACTGTG | 55819 |
| rs546832722 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179941215 | CTGCTTCGTTTGGTT[A/G]GTTTTTAATGGATTG | 55819 |
| rs546839278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977133 | CCTGGAACCTGCTAT[C/T]GGCTCACCATCCTTC | 55819 |
| rs546841545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977783 | CATGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG | 55819 |
| rs546909822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050243 | CTGCAGGGTGAGCTG[C/G]CAGGCTGGAGACCCA | 55819 |
| rs546925044 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009681 | GTTTCCTACAGAACT[A/G]AATATGCACTTATCT | 55819 |
| rs546938222 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059468 | GCAGGAACTTCCTGT[C/G]CTGTCTGGAACTCAG | 55819 |
| rs546944170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180005085 | CATAGCTCCTTCTCC[C/T]TAAGTCTCTCGCACC | 55819 |
| rs546949369 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924410 | TGAGGCAGGAAAATC[A/C]CTTGAACCCAGGAGG | 55819 |
| rs546949672 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070684 | TGTGCAAAAGGTTTC[C/T]TTCAAACCATGACTA | 55819 |
| rs546951800 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179956184 | TTTGACAAGCCCCTG[A/C]GCTGCCCGAGCTCCT | 55819 |
| rs546960993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179998109 | CTCCCAAAGTGCTGC[A/G]ATTAGAGGCGTGAGC | 55819 |
| rs546961797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071326 | CCACGACGGAAGCCT[C/T]GACCCTGGCTGGGGC | 55819 |
| rs546999241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180043468 | AAAATATGTGAGCTA[C/T]CCCACGCTCAGCAGC | 55819 |
| rs547049955 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946648 | AAGCTCCGCCTCCCG[G/T]GTTCACGCCATTCTC | 55819 |
| rs547067485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956878 | TGCTTGGCACAAGCC[C/T]GGGAGCCTACTTGGG | 55819 |
| rs547075522 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033210 | TGGTTTTAAACTCCT[A/G]GGCTCAAGTGATCCT | 55819 |
| rs547088351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179994045 | AGTTGTAGATGTGTG[A/G]TATTATTTCTGAGGG | 55819 |
| rs547105741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035248 | CGTTTGGTTCCAAAT[A/G]TTTTTAAAATTTCCT | 55819 |
| rs547106683 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046113 | CCACGAGAATCTGTG[C/G/T]GCGGTGGACCGCGGC | 55819 |
| rs547113310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940585 | TTATGAGAATTTCAT[C/T]TCAATTTTAAAAACT | 55819 |
| rs547153785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949290 | TTTTTTTTAAGACAA[C/G]GTCTTGCTGTGATGC | 55819 |
| rs547154064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071035 | TTTTATATTAGAAAA[C/G]GGCCGCATCCTTCCA | 55819 |
| rs547179204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028855 | TGAAGAAAAAGTATA[C/T]TTAGAAATTTTTTTA | 55819 |
| rs547224303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933070 | AGAGGAGCGATTACC[A/C]GGGTGTTATTTAATG | 55819 |
| rs547229008 | snp | G/T | 1.64808e-05 | 0.00287057 | intron-variant | RNF130 | GRCh38.p7 | 5:179980243 | ACTAAGTGTAAGATC[G/T]CTGAATGACGTACTT | 55819 |
| rs547241058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981001 | CTAGGAGGGGTGGGG[C/T]GAGGCAGGGGAGGAA | 55819 |
| rs547247644 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180021329 | TGTGGCTCGTGGTTC[C/T]CTCCTCCGGAAAAAC | 55819 |
| rs547249932 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972479 | ATATGATGCTGTGAC[C/T]TCTGATCAAGGCTCT | 55819 |
| rs547285694 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923555 | GGAGCTGAGTCTCAG[C/T]CAATCCCAGCGGCTG | 55819 |
| rs547294216 | snp | A/G | 0.000750871 | 0.0193616 | intron-variant | RNF130 | GRCh38.p7 | 5:179966790 | GCCCTGTGCCTGAGC[A/G]GAGGCCCCCACTTAC | 55819 |
| rs547325741 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038250 | TGTAGAGATGGGGTC[-/TC]CCTATGTTGCCCAGG | 55819 |
| rs547326200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974498 | AATAGTGCGACAGAA[A/G]AGGAAAAGGAAACGT | 55819 |
| rs547364408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934008 | AACCTGCCTGTGAAG[C/T]TCACAACAGTGTTCC | 55819 |
| rs547379482 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001984 | ATGCACAACTGCTCA[C/G]TCTGGCCAAGGCACC | 55819 |
| rs547389657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054213 | ATGCTGGTTTCTTCA[A/G]TTAATCACTCATATT | 55819 |
| rs547401559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010104 | TACAAAAAATTAGCC[A/G]GGCACGGTGGCAGGC | 55819 |
| rs547406869 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963972 | TCATTTCTGCAGGGC[C/T]TTCATTCTTAGTCAA | 55819 |
| rs547410614 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935117 | ATTCATGACTTTTTC[C/T]TTTGGAAGTATATTG | 55819 |
| rs547415131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016603 | CCCATCTGTGATCCC[C/T]GCTTCCAACTATTTT | 55819 |
| rs547423657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179929635 | TGCCTGTAGTCCCAG[C/T]TATTCAGGAGGCTGA | 55819 |
| rs547436201 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049863 | GACCGAATTTCATTT[-/C]CCCCCTTTTCCTCAT | 55819 |
| rs547442780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994654 | GTTACAGTAGTGGTG[C/T]ATCGGGTGGGTGAGC | 55819 |
| rs547459461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922891 | GTGAGCCGAGACTAC[A/G]CTACTGCCCTCCAGC | 55819 |
| rs547520685 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039808 | AACAAAACTAGGGTG[A/T]GAGCCCTCTTCTGTT | 55819 |
| rs547553569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943710 | TAAAACTGAACCCAA[A/C]GCCAAGTTATCTTTC | 55819 |
| rs547572909 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180055517 | GTCTGTCTCATGTGG[C/T]ATACCAGTTGTCCTA | 55819 |
| rs547581245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032159 | TAGCTTATCTTTTCA[C/T]TGTTTTTCAATGGTT | 55819 |
| rs547599323 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034569 | GAGTCAATTCTGACA[A/C]TCTGTATATTTTTAG | 55819 |
| rs547624175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937270 | CGAATACACAACTTA[C/T]AGAATGGAGAAAACA | 55819 |
| rs547629405 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981826 | TGCTCCGTCTTTGAA[A/G]CCTAATCTATGAGTC | 55819 |
| rs547651982 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073754 | CCTCGCCCTGGGCCT[C/G]GCACCTAAAGAGTGC | 55819 |
| rs547655687 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030019 | CGCCCGGCTAATTTT[C/T]GTATTTTTGGTAGAG | 55819 |
| rs547663694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995819 | TCCCAAATTTCTCTT[A/T]CCCAGTGTCTGAAAT | 55819 |
| rs547674776 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016446 | TGTAAATATCAAAGC[-/A]ACATTTGGGACATGC | 55819 |
| rs547682746 | in-del | -/T | 0.22263 | 0.248497 | intron-variant | RNF130 | GRCh38.p7 | 5:180003688 | GTCTAAAAGCCACTA[-/T]TTTTTTTAAAATTTT | 55819 |
| rs547683942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974745 | ACTGGGAAATGCGAG[C/T]GTCACGAGATGCCGG | 55819 |
| rs547689658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042202 | AAGATGCCAGTAACT[A/T]CAGAGAACTATTACA | 55819 |
| rs547700870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066757 | CAGGAAGGCGGAACC[C/T]GGGAGGTGGAGGTTG | 55819 |
| rs547740567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021226 | ATCACCTGATCTCAT[A/G]ATCCGCCTGCCTCGG | 55819 |
| rs547764159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938049 | CACAACCCAGACTCC[C/T]GGGCTCAAGTGATCC | 55819 |
| rs547787724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180067388 | CAAAATCACTGGCAC[A/G]GCAATAGAAGACCTT | 55819 |
| rs547798293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179930150 | GCGACCTCTGCCCCC[C/T]GGGTTCAAGCGATTC | 55819 |
| rs547824011 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180060563 | TTTTACCAACACACC[A/G]CGAGGGCCTGTCCGT | 55819 |
| rs547879800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926421 | GAGGCCGAGGCAGGC[A/G]GATCACCTGAGATCA | 55819 |
| rs547880446 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981805 | AATCCACACACTGCG[C/T]GTGGCTGCTCCGTCT | 55819 |
| rs547903064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180056013 | TGCTTGAACCCGGGA[A/G]GCAGAGGTTGCAGTG | 55819 |
| rs547907715 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066444 | GAAAACAGACTAATA[C/T]ACCTTCCCAATATGA | 55819 |
| rs547917410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179957949 | GTGGCGGGATCTCGG[C/T]TCACTGCAAGCTCCG | 55819 |
| rs547973962 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179958428 | GTCTGAAAAACACTG[C/T]TTTTGATATTTAAGG | 55819 |
| rs547980663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996500 | GTATGTTCTTTCTAT[A/T]CCTAACTTGTTAAGA | 55819 |
| rs547980865 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006724 | ACTTTGAAATTAAAG[G/T]TGCAATATTAACCAT | 55819 |
| rs548012606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058191 | AAGGGACCTGAGGTG[G/T]TCTGCAAAGCTGGCC | 55819 |
| rs548034909 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180067967 | AACATGAAAACCTAA[C/G]ATTCACTTTTTTGAG | 55819 |
| rs548047262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951528 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 55819 |
| rs548073375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044764 | TTGAACCCAGGAGGC[A/G]GAGGTTACAGTGAGC | 55819 |
| rs548104099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051908 | AGATGCTACAGATCT[A/G]AATAACTGAAAATTA | 55819 |
| rs548109218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945598 | AGCAGGACTCACACC[A/G]CGGTGGACAGTCTAA | 55819 |
| rs548130010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942320 | TCATCAGTTGAGGAC[A/T]GATTCAATATACAAT | 55819 |
| rs548131795 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179925795 | ACCTTGGCCTCCTAA[A/G]GTGCTGGGATTACCT | 55819 |
| rs548148575 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180037638 | AGACTTACTGAATCA[C/G]AATTTGCATTTTAAC | 55819 |
| rs548164651 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954641 | CTGATAGTGGTGATG[C/G]TTGCACAACTGTGTG | 55819 |
| rs548179272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070594 | ATTCTCAGGGTGACA[A/G]TGAGGGTGGGGATAA | 55819 |
| rs548186894 | in-del | -/CA | 0.00199481 | 0.0315187 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072923 | ACCTTCCGAAACGCG[-/CA]CGCGCGCGCACACAC | 55819 |
| rs548205151 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF130 | GRCh38.p7 | 5:179958022 | AGCTGGGACTACAGG[C/T]GCCCGCCACTACGCC | 55819 |
| rs548261167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057804 | TCCTGAGTTCTATGA[A/G]CTGTTATATAGCAAA | 55819 |
| rs548294501 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003563 | CTTCTGAATTATCCT[C/T]TGAGTTTTTAATCAG | 55819 |
| rs548297953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966729 | AGGCTGAGGCGAGTG[A/C]CTTGACTCTCCTGAT | 55819 |
| rs548308143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960766 | GTCATTAAAATGCCA[A/G]GAGATGAAATCTATT | 55819 |
| rs548316530 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030484 | GTCATTTCCATCACC[C/T]CCCAGAAAATTCACT | 55819 |
| rs548324102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979368 | GCAATGGGAATAAAA[C/T]GGGTAAAGTCCAAGA | 55819 |
| rs548364041 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179999005 | CTTTTATTTTTCAAT[A/G]TTTTATTTTATTTTG | 55819 |
| rs548374150 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072307 | AGGCGTGATAGCCGC[A/G]GGGCGTGGAGCCCGG | 55819 |
| rs548380615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065897 | ATTCACAACTGCCTC[A/G]GAATAACTTTCAATT | 55819 |
| rs548434819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179934804 | ATGCCTCAGCCTCCC[A/G]GGTCACGTAATTCCA | 55819 |
| rs548439570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022843 | ATGCTTACATTTATG[C/T]TTTCTTACAAGCTTT | 55819 |
| rs548452044 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002103 | GGGAGCTGCTTCAGC[C/T]TAGGTACTGGGATGT | 55819 |
| rs548469807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059327 | CATTTATGCTCTCAG[A/C]ATCCCGATGCTTTCC | 55819 |
| rs548474106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962877 | GTCCTTCCTTTTACC[A/G]ACGTGAAGCCTGCCG | 55819 |
| rs548476691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992378 | CGATCTCCTGACCTC[A/G]TGATCCACCCACCTC | 55819 |
| rs548512309 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960933 | TTGAAAAATTCATTA[A/G]TAACGAATAATTACA | 55819 |
| rs548515554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179948363 | TTTCACCGGGACTCT[A/G]TTCTTTGTTCTGTTT | 55819 |
| rs548517724 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059202 | TTCCTTGGACTGAAA[C/T]ATCCTCCTTTCTGCC | 55819 |
| rs548529010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030018 | ACGCCCGGCTAATTT[C/T]TGTATTTTTGGTAGA | 55819 |
| rs548540182 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041547 | GAAGAAGCCCCCGGC[G/T]GCTCTTCCCACTCCC | 55819 |
| rs548547411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993059 | GGACATGAACACATC[C/T]TTTTTTATGGCTGCA | 55819 |
| rs548549305 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928975 | CTTAATTTTAGTGTG[C/G]AACAAATTATCTAAC | 55819 |
| rs548554304 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180061512 | GAGCAGGGCTGATTC[C/T]TACTGGAGGCTCAAG | 55819 |
| rs548634915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053382 | AGTTTACAAAATCCT[A/G]GGCAAACAAAGCTCA | 55819 |
| rs548651480 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043175 | ATAAAAAACAAAAAA[A/T]TTAGCTAGGCATGGT | 55819 |
| rs548656527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978412 | AACTGAAAAATGATT[A/T]AAATTATTTTGTTTT | 55819 |
| rs548674289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033173 | TTTTTGTAGAGACAG[C/G]GTCCCCCTATGTTGC | 55819 |
| rs548695973 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179939168 | GTTGCAGTGAGCTGA[C/G]GTCGCGCCACTGCAC | 55819 |
| rs548721499 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023534 | GCTCAAAAACTAAAC[A/T]AAACCAAAACAAAAA | 55819 |
| rs548733561 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072738 | TGATCTGACAGGAGG[C/T]GGAGCTCAGGCGGTG | 55819 |
| rs548738543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068130 | CCAGCACATCTGCAT[A/G]CATAATCACATCATC | 55819 |
| rs548774472 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043471 | ATATGTGAGCTACCC[C/T]ACGCTCAGCAGCACC | 55819 |
| rs548774830 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180068634 | ATGTTATTCAGAAAT[G/T]CACACGTGCCAAACT | 55819 |
| rs548794356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970300 | CAAATATAGCCAGTG[C/T]TTTCTTCTGTGTCTT | 55819 |
| rs548820511 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000105 | ACTCTCTCAAGATGT[A/G]TAACTTTCTCAATTT | 55819 |
| rs548823564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015741 | AAAGGAGTAGGAAAA[A/G]GAGTAGGAAAGGAGT | 55819 |
| rs548823580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007779 | CTCCTTCATCAGCCC[C/T]GGCCCCACACTGGGT | 55819 |
| rs548855794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179964714 | CTTTCAAAAGGTCAC[A/G]CAGCACTGCTCCTGG | 55819 |
| rs548856697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968329 | AAAAAAAGAAGGCGG[C/T]GGCTAGCGGTAACAA | 55819 |
| rs548861659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027109 | CACTGCTTCTGCCCT[A/G]TGATGAAGGGAGGGC | 55819 |
| rs548873088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180039937 | AAACTCATCGCACAG[C/T]GCCTGGCATTTATAT | 55819 |
| rs548886670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965194 | GTAAACACCATCATA[A/G]AACACCCAATATGCT | 55819 |
| rs548906698 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179931101 | TGCTTTTTTTGTACC[C/T]ATTAAGATAAAAACA | 55819 |
| rs548914392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180060973 | ACGCGGGAGGCTGAG[A/G]CAGGAGAATGGCGTG | 55819 |
| rs548935247 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179975523 | TAAAGTTAATTTTTG[C/T]TACACCTGATAACTG | 55819 |
| rs549038117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990189 | TGCCTGGCTGCACTG[C/T]TATTTATTGGATACA | 55819 |
| rs549043966 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179989335 | CGACACAGCCAAATC[A/G]TATCAGCCGGATACT | 55819 |
| rs549046829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180033754 | GTATAATGACTTTGT[A/G]TTCTACATTCTTTCA | 55819 |
| rs549047401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925046 | CCATATTGTGAAAAG[C/T]GTATTTGGTTTTTAT | 55819 |
| rs549071835 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941457 | CCTTTGGGGATCCCA[A/G]TGGAAGGCCTGGGAT | 55819 |
| rs549106762 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026295 | AAACTACAGCTAATT[A/C]TATCAGACAGTGATT | 55819 |
| rs549114539 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006060 | GACATGAAAAACAAG[A/G]TATCAGAGTATTTGC | 55819 |
| rs549116394 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180004941 | TTTCCCATTTTTTTT[C/T]CTCAAAAGAAGCCTC | 55819 |
| rs549148824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990766 | GGCTCACACTCTTGT[C/G]TTCTGGTCACTTCTC | 55819 |
| rs549156350 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180018764 | GCTGACCAACACAGT[A/C]CTGCCAGCTACAAAA | 55819 |
| rs549159065 | snp | C/T | | | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966837 | GATTTCTCCTGTTCT[C/T]GGAGTGAGCTCCCCA | 55819 |
| rs549161886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924131 | GGGAGGATCGCTTGA[C/G]CCCGGGAGTTCAAGT | 55819 |
| rs549168173 | snp | C/G | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014894 | AGGAGGCTGAGGTGG[C/G]AGGATCACTGGAGTC | 55819 |
| rs549197728 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989686 | TCTATTCAGTCAGGC[C/T]GTATCTTTTAAGCGG | 55819 |
| rs549207809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983217 | CATATTAAGGAAGCT[C/T]TGCCTATTTCAAGGT | 55819 |
| rs549214907 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931188 | GTGACAGTGTTTCCC[A/G]CCTGAAGTACCGCAC | 55819 |
| rs549217780 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180019468 | AGGGTCAAGCTGCAC[A/G]TGGGGCAGAGCCCTG | 55819 |
| rs549220487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953069 | TGATCTCTATGTACA[A/G]ATGACATGATCTTGT | 55819 |
| rs549223844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010825 | CCTGACCGTGTTGTT[A/G]GTCATGTGAATCTAC | 55819 |
| rs549285541 | snp | C/G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987766 | TGATGTGAAACATCA[C/G/T]GACTATTGACTTGCA | 55819 |
| rs549364073 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180034444 | AAGGATTAGTATTAT[G/T]TTTTCTTTAAATATT | 55819 |
| rs549366550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997282 | GAGTAGCTGGGATTA[C/T]AGGTGCACACCAACA | 55819 |
| rs549373385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000708 | ATGTTTTTTCATTCA[C/T]TGAATTCTTCAGCTG | 55819 |
| rs549393027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959094 | AGTCAACATGAGGCT[A/C]TTTTGAGTATTAAAC | 55819 |
| rs549434417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993212 | GTCTTTATAGCAGCA[C/T]GATTTATAGTCCTTT | 55819 |
| rs549440995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180010560 | GAGATGGGGTTTGCC[A/G]TGTTGGCCAGGCTGG | 55819 |
| rs549454464 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179952585 | CTTATAAATATAGAT[G/T]CAAAAATCCTCAGCA | 55819 |
| rs549455556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050020 | TAGGGCTGCCAGAAC[A/G]AAGTACCACAAGCAT | 55819 |
| rs549457872 | in-del | -/TAAGA | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179948847 | ATGGACTTATCAGGC[-/TAAGA]CTGCCTTAAGCTGCT | 55819 |
| rs549465898 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:180057323 | GGAGGCCGAGGCGGG[A/T]GGATCACCCGAGGTC | 55819 |
| rs549491898 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057701 | TGGGACCCTTCCAGA[C/G]CTTACCCTATGTACC | 55819 |
| rs549500484 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941231 | GTTTTTAATGGATTG[C/T]TGGACATGTATACAA | 55819 |
| rs549506771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043320 | ACAGAGCAAGACTCT[A/G]TCTCTAAAAAACAGT | 55819 |
| rs549523859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180035153 | TATCTTTGTTTACTG[A/G]CCTAGGTATTTAAAG | 55819 |
| rs549547395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962177 | CTAGTGGTTCACCTG[C/T]TGGATGAGGTGCAGT | 55819 |
| rs549574220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946623 | CAGTGGTGTGATCTT[A/G]GCTCACTGCAAGCTC | 55819 |
| rs549605986 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951584 | GAGACGGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 55819 |
| rs549607459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976371 | TTCTGGAGGATCCTG[C/G]GCTGAAACAGCAAGA | 55819 |
| rs549610547 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955408 | AAACACAAACAAATG[C/T]AATCTGGGTCTGCGA | 55819 |
| rs549628900 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038128 | GTGTGATCACGGCTC[A/G]CTGTAGTCTCAACTT | 55819 |
| rs549634443 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179987518 | TGACTTCCAGCACTA[C/T]GTGGAACAGAGGGGG | 55819 |
| rs549669006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971808 | AAAAGAGGTCTAGAG[A/G]ACTCAGTTTCTACTG | 55819 |
| rs549684784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940563 | CTTTCAAATGGTTAC[C/T]TTTATGTTATGAGAA | 55819 |
| rs549700463 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039089 | TTCTTTTGCTTTCCC[C/T]GAATAAATTAAAAGT | 55819 |
| rs549714247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023824 | GAGCATAAATCCCCA[C/T]TTATTAAGTGTGGGC | 55819 |
| rs549726741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180024392 | GCAGGGTTTGCAGAC[A/G]TTCTTTGTACTATCT | 55819 |
| rs549745708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941152 | GGATCTATTTCTGTT[A/C]TTTGTTTTTTCTCCT | 55819 |
| rs549758767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180008591 | GTAACACTAAGATAA[C/T]AGTAAAATCTTGGCA | 55819 |
| rs549776817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979525 | ATTTTCCCATTCTAG[A/C]TAACCTTGAATACTC | 55819 |
| rs549781756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921289 | TCTTTCTACCCTACT[C/T]CTATTGCCAGGGAAA | 55819 |
| rs549782431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016531 | GCGGCCACGCTCCCA[C/T]GCACTTCCACGTCTG | 55819 |
| rs549818180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001285 | AAAGTGATCCCTCTT[G/T]GTGTGAGGTCTGATG | 55819 |
| rs549818815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180052857 | GTTCTTAATCTGAGA[C/T]GTCCATAAACCAATA | 55819 |
| rs549848521 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179962728 | ATAACAGTCATCTAG[C/G]CCAATCCTCCATCCT | 55819 |
| rs549855496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053231 | CTGCAGAAGAGATCT[C/T]ACCCCTCCGCTTCCA | 55819 |
| rs549859078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179956113 | TCTCACAGGAATCCT[C/T]CAGACCTTGTGTGTG | 55819 |
| rs549874551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928870 | TCCTGATCTCGTGAT[C/T]CCCCTGCCTCGGCCT | 55819 |
| rs549898383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045531 | GCGGAAGTGGACCTC[C/T]GCACGTTGCCGCTGC | 55819 |
| rs549904957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922801 | TAGCCAGGTGTGGTG[A/G]TGAGCACCTGTAGTC | 55819 |
| rs549909666 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030502 | CAGAAAATTCACTCA[C/T]GCCGTTTTTAAAAAT | 55819 |
| rs549912356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046091 | CCATGGGGAGGCATC[A/T]GAGGCCCCACGAGAA | 55819 |
| rs549943672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923176 | TTATAGTTTTAGTTC[C/T]CACACTTAGATGGTC | 55819 |
| rs549975776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949249 | GGGATTACAGGCATG[A/G]GCCACCGTGCCCAGA | 55819 |
| rs550016759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047468 | GTTTTTTTCTGGCCC[A/G]GCGTGGTGGTTCATA | 55819 |
| rs550038205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054711 | TTGACTACTGTGAGT[C/T]CCTTTTACTTCCATA | 55819 |
| rs550070080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040915 | AAAAATAAAAAAGGA[C/T]TGATAATATCCAGTA | 55819 |
| rs550077804 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072867 | AGGTGAACTACTCCA[C/G]GGGCCCCCGGACCAG | 55819 |
| rs550102596 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180047961 | CCCTGGCGTGGGCCC[A/T]GGACTCTCCAGGGTT | 55819 |
| rs550115422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937123 | AAATATCATCAAAAC[A/G]AAATATCATCAAAAC | 55819 |
| rs550121127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019831 | AGAAAAATAAAGTGC[A/G]AACTCTTTCACTGGA | 55819 |
| rs550131791 | snp | A/G | 0.000214145 | 0.0103454 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179980192 | CTTGGCTGCATCTCC[A/G]AGACGACGCTATGAA | 55819 |
| rs550142837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957222 | TTTGAGACCAGCCTG[A/G]CCCACATGGCAAAAC | 55819 |
| rs550146491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944204 | TCGAACTCCTGACCT[C/T]GTGATCTGCCTGCCT | 55819 |
| rs550181603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974153 | TCCCAGACAAGAACT[C/G]TCTTCTGCTAGCTGG | 55819 |
| rs550201946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066709 | GTGCTTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs550258637 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943865 | AATGGCAACATAAAT[G/T]AGAAAATACACTTTT | 55819 |
| rs550258819 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179968922 | GTGTCACTAATGCCC[A/G]ATACTTTGAGAAATC | 55819 |
| rs550263779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940484 | CTTCATGATCCTCCC[A/G]CTTTGGCCTCCCAAA | 55819 |
| rs550274099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068929 | AACATGTCAAGAATT[A/C]TCCTCAATTCAAAAT | 55819 |
| rs550276956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060419 | CAAAGCATCTGATTA[C/T]GTCTTTTATGGTATC | 55819 |
| rs550290641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057461 | GGCTGAGGCAGGAAA[C/T]TGCCGGAACCTAGGA | 55819 |
| rs550297820 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020498 | GAACCTCCTGCCATG[A/C/T]GTCTGCTGGGAAGCC | 55819 |
| rs550301003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021156 | TATTTTTAGTAGAGA[C/T]GGGGATTCACCATGT | 55819 |
| rs550303112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925670 | AGAAACTGGGACTAC[A/T]GGTACATGCCACCAA | 55819 |
| rs550310144 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045782 | TCTCCAAGTCCCCAC[C/G]AGATTAGCTAGACAC | 55819 |
| rs550312031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179932148 | TAAAGTTACCTGTTA[C/T]AGGGTGTTCCTTCAG | 55819 |
| rs550318081 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969503 | CTAAAGGTAGGTACT[A/G]GAATGAAGAAAAATC | 55819 |
| rs550343738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926349 | CCTTTGCAATATCCT[C/T]CATAATAAATCTCAG | 55819 |
| rs550360083 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975977 | CCCGGGATGCTTCTG[A/T]AAGCCTCCCACTGAC | 55819 |
| rs550376424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057666 | CACCCCCGCAATACC[A/G]CGACAGAAGCTCCTG | 55819 |
| rs550376550 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180050382 | GGAGTGTCACTTTTT[C/T]GTTCTATTCATGCCA | 55819 |
| rs550406268 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923143 | TAAGATTTTCTCGTA[C/T]ATGTTCATCTAGAAG | 55819 |
| rs550413537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051194 | TTGTAAATAAAAAGG[C/T]GATACATTCTTACAA | 55819 |
| rs550432471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964046 | GCTCCCAGCCGTCTG[C/T]GAGCCGGCCTCCCAT | 55819 |
| rs550441963 | in-del | -/ACCGGGT | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179964237 | AGGGGCGGGCGACTG[-/ACCGGGT]ACTTGGCCACCACAG | 55819 |
| rs550459696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951091 | TGGAGTTGGTTCAGA[A/G]GAGGGCCACTGAACC | 55819 |
| rs550465888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179995698 | CTCCTGTGGCCTGGA[C/T]TGCACACTTCCCCAG | 55819 |
| rs550468907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954121 | GAGGTTGTGAAGAAA[C/T]TGCAACCCGCATACT | 55819 |
| rs550501663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180051793 | AAAAAGCATCTTAAG[A/G]GTAAGTTTAAATGAC | 55819 |
| rs550519585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931411 | TGCTTTAAGTGTAGC[A/T]TTTTTGTTTTTTGTT | 55819 |
| rs550533047 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986657 | TGTTAATTTTATGCG[A/G]TTATGATTTAACATG | 55819 |
| rs550534551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044653 | CCTGACCAACACAGC[A/G]AAACCCCATCTCTAC | 55819 |
| rs550539052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966612 | TATTCCTATTAATTA[C/T]ACACAAACACACCAG | 55819 |
| rs550554551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180017512 | GCCTGAATCTGTTAC[A/G]ACAATGGTATTTGTA | 55819 |
| rs550578588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975770 | CATAGAGGGTGCAGC[A/G]AAATTCCGTGAACCG | 55819 |
| rs550617194 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043993 | CTGTAATTAAGAAAA[C/T]ATAAATAATGAAAAC | 55819 |
| rs550644788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947622 | TCCTCATCTGTAAAA[C/T]GGAGTTAATAAGAGG | 55819 |
| rs550645907 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964898 | TTTAATCAGCATGAA[C/T]ATTCAAAAACACATA | 55819 |
| rs550662841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067919 | TCATTAAAGGAACCA[C/T]TAAAGGCTTCGTCTA | 55819 |
| rs550670265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966023 | GCAACCAGGAAGATG[C/G]GTGAAAGGTTGTTAG | 55819 |
| rs550683410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070488 | TTAGTATCTTAAGAG[C/T]GTACAAGCAAATCAT | 55819 |
| rs550684355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012689 | GGAAAGAATTTCACA[C/T]AGGAAGGGGAAGAGT | 55819 |
| rs550728819 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180071366 | GGCAGCGCGGGAGAG[A/C]CAGGGCCAGAGCCGG | 55819 |
| rs550747441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005118 | AAAAGAATTGTATAT[C/T]ACTCCACTGCTAAAA | 55819 |
| rs550767425 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072279 | AGCCGCTGGTGCTGG[C/T]TGTTTCTCTGTCAGG | 55819 |
| rs550781500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036827 | GAATATAATGTCTGT[C/T]TACCCCCACACTCAG | 55819 |
| rs550808440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179973382 | GTCTCTTCAGTGCAA[C/T]TTTCACTGAACTCAC | 55819 |
| rs550820066 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927309 | ACACCAGATGTGTAC[C/T]GGTCAACTAATTATT | 55819 |
| rs550820406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179967381 | GTCCATGTTGAAGAA[C/T]CCCAGGTAATAGAAA | 55819 |
| rs550840687 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179942241 | GTTGTTATTTCTGTA[A/C]CATCAGTTATGGTAG | 55819 |
| rs550862363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044225 | TACCTGCCAACTTTT[A/G]TAAGAGGATACTATC | 55819 |
| rs550881262 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922008 | ACTGTGTGACAGAGT[A/G]AGACTCCGTCTGAAA | 55819 |
| rs550882140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968039 | GGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG | 55819 |
| rs550928965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957810 | GTTAATTTTAAATCT[C/T]TTCTGGAATTGTTAC | 55819 |
| rs550950468 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969964 | CCATTGTACTCCAGC[C/T]TGGGCAACAAGAGCA | 55819 |
| rs550958805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984404 | CATTAAATATAATGG[G/T]GGCTGTCAGTTTTTC | 55819 |
| rs550965051 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179946832 | GTGCTGGGATTACAG[A/G]CGTCAGCCACCGCGC | 55819 |
| rs550985669 | snp | A/T | 0.0640965 | 0.167152 | intron-variant | RNF130 | GRCh38.p7 | 5:180065136 | CTACAGAATGAATTT[A/T]AAAAAAAAAAAAATC | 55819 |
| rs550986978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991738 | GCACATTACATTTAT[A/T]GTGCCCTTTATTTCT | 55819 |
| rs550997923 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180044347 | TACTACAGAACTTAA[-/T]TTTTTTTTTCCTCTA | 55819 |
| rs551010704 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041334 | TCAAGATACACTTAC[C/T]GTATCCATCTGTCTA | 55819 |
| rs551031017 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921625 | CTACGTAGTGAAACC[C/T]TGTCTCTACTAAGAT | 55819 |
| rs551038535 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179926492 | CTCTATTAAAAATAC[-/A]AAAAAAATTAGCCGG | 55819 |
| rs551041500 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179950956 | AGGAACTATACCATG[A/C]ATCTACGAAATACCA | 55819 |
| rs551077541 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043755 | AAACAAATCCAACAA[C/T]GGCCTGTATAAGCAA | 55819 |
| rs551098340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987776 | CATCATGACTATTGA[C/T]TTGCAAATGCCAAAA | 55819 |
| rs551129377 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073788 | AATCTGGTCCCCTCC[A/G]GCTGGACCCTTCATA | 55819 |
| rs551137041 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180064763 | TTGTCATCTGTGTTT[-/G]TAGAGTCTCAAGCTT | 55819 |
| rs551144318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029955 | CTGGGTTCAAGGATT[C/T]TCCTGTCTCAGCCTC | 55819 |
| rs551160746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064326 | CAGCAAGCAAAGGGA[A/G]AAGAGTGGGAATCTT | 55819 |
| rs551175757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014334 | GAGAAACTTCTATCA[A/C]TCTATCAGCGATTGT | 55819 |
| rs551177282 | in-del | -/AAAAACACGCC | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180065033 | TTTTCTTACTAGAGA[-/AAAAACACGCC]TTTTTCAACATTTTC | 55819 |
| rs551202818 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179978378 | CTTTCTGTGGCTACT[A/T]TGGTAAGCAAGTGTT | 55819 |
| rs551211420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974805 | GCCAGCCAAGAGAAC[A/G]AGGCCCCGAGGAAGG | 55819 |
| rs551235936 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017285 | GTCCCTCCTCAGCTC[A/G]TCACTTCAGGAAGTG | 55819 |
| rs551286310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067489 | AAGAGAGAAATGGGG[C/T]GGTAGCAGGACAGGG | 55819 |
| rs551286987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970213 | ACCTTCTCTTCCAGG[A/T]GTTCTCTGAGATGGA | 55819 |
| rs551308104 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972090 | CCAGATACATTCAGT[A/G]CACCTAAGGCGTTAT | 55819 |
| rs551314405 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004912 | CACCCTCCTTCATTC[A/G]TTCACCACCATTTTT | 55819 |
| rs551328810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180014782 | CTTGAGCTCAGGAGT[C/T]CAAGACCAGCCTGGG | 55819 |
| rs551336870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179920788 | ATATATTTATATATA[G/T]ATATATATTTTTTTT | 55819 |
| rs551338880 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179927886 | TGAGCCACCATGCCC[A/G]GCCTAGCTTTGTCTA | 55819 |
| rs551363887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180017783 | GCCAACAGAAGGAAC[C/G]TCAGAATTAAGCTCC | 55819 |
| rs551401091 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957498 | CCTTTAATACTCATG[C/T]TGCAACTGCATTTTT | 55819 |
| rs551406601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964228 | ACAAGTAGGAGGGGC[A/G]GGCGACTGACCGGGT | 55819 |
| rs551415702 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061696 | ATAAGGACATTAGTC[A/G]TTGGATTTAGGGCCC | 55819 |
| rs551429612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988515 | TTGAAATATTTCTAA[C/T]TGTCTGATTTAGGCA | 55819 |
| rs551444162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180040801 | CCACAAACAATACAA[C/T]GAAGCTGAATCAGTA | 55819 |
| rs551490240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004181 | CTAAAAGGAGCTCTC[A/C]CATGATTCTTTTGTA | 55819 |
| rs551503551 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972313 | AAAAGTCACGGGGAC[A/G]CAAATGCCTAGTACC | 55819 |
| rs551552119 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944373 | ATGATGGAAACTTCA[C/T]TGTGTTCCTATAATT | 55819 |
| rs551581727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965132 | CCCGTATTTGCATGT[C/T]TTTGTGTGTGTGTGA | 55819 |
| rs551591933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959025 | TCTGCCTCCCTGTAG[A/G]TATCGCCAGAGCTCC | 55819 |
| rs551594031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041745 | GAAAGGGAACACAGC[A/G]CATGGATCTAAAAAG | 55819 |
| rs551630469 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179936542 | CCAACTTTATTTTCA[A/G]TGGCTTTCCCCACTA | 55819 |
| rs551642191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068095 | AAAGCAAGAAGTGGC[C/T]GATACTAAACTCTTC | 55819 |
| rs551679168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026087 | TGGAAAAAAGGTGAA[A/G]AGCCATTCAACTAAT | 55819 |
| rs551679915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060930 | AAAAATTAGCTGGGC[A/G]AGGTAGTGGGCGCCT | 55819 |
| rs551714527 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963848 | AAAAAGTGTGCGGTG[A/G]AAATATGTATATAAA | 55819 |
| rs551745223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923323 | CACTGAACTGTCTTG[C/G]CACCTTTATGGAAAA | 55819 |
| rs551754542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990667 | GCTAGACCATGGTCC[A/G]CTTGGTAATGGGCGT | 55819 |
| rs551769942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007077 | GATCTCTTTGGTAGC[A/G]TGTTCTACAGGAAGA | 55819 |
| rs551775038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043275 | GATTACAGTGAACTA[C/T]GATCATGTCGCTGCA | 55819 |
| rs551783890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923987 | ATTTCAGTGCTAGCT[C/T]ATGAGCTGCAGGGCA | 55819 |
| rs551785022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964653 | TTGTGTGTGCATAGG[C/T]ATTTTTCTAGAAAAA | 55819 |
| rs551836381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035018 | AACTTTTGGGTTTCG[C/T]TGACTTTCTCTATGA | 55819 |
| rs551836749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014256 | TCCTATGGACAGCAG[C/G]AAACTGCTATCCCTT | 55819 |
| rs551838539 | in-del | -/AAGTCA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978462 | GCCCAAATTATGTCT[-/AAGTCA]ATCTATTTTGTTTTA | 55819 |
| rs551846424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179958586 | CCTGTGAACAGGTCT[A/G]TCCTGTAGCTTCTGT | 55819 |
| rs551860534 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064128 | TGTCCATGGATTTAA[C/G]CCTATTTATGGAATA | 55819 |
| rs551877964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007540 | GCTGCCACCTTCTTA[C/T]TAAACTTTAATAAGC | 55819 |
| rs551878349 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036748 | AATCCTACCTTATAA[A/G]TATTTCACAAAGTTT | 55819 |
| rs551878619 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009388 | AATACATAAAAAGCT[C/T]TCAAAATTCAACAGT | 55819 |
| rs551913793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179967294 | ACAGGCACAGGGAGT[A/C]GTAATCATTAACATA | 55819 |
| rs551920001 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029300 | GAAACAGTGATCTAT[A/G]AATTGGATGAAGTAT | 55819 |
| rs551924531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042404 | TCCTTAAAAGGTTTC[C/T]GCACTCTGAACCTTT | 55819 |
| rs551943305 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180000627 | GTTAATTTCAAATAA[A/C]CTATCTTCAAGTTGA | 55819 |
| rs551943671 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180048771 | TCTGTAGCTTCAGCT[C/T]CATCCTAAGAGTCCC | 55819 |
| rs551955145 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990161 | AGATGCGGAGACCAG[A/T]AGTGGCCCCGAATGC | 55819 |
| rs551964143 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039821 | TGTGAGCCCTCTTCT[G/T]TTGGCCCTTACCTCT | 55819 |
| rs551974737 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179945714 | GGGACAATGGAAATT[A/C]AATTTGCTTTGCCCT | 55819 |
| rs552055927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030883 | ATTTACAGCTGAGAA[C/T]ACCACCAGTGTGAAC | 55819 |
| rs552065556 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967093 | GATTCTAAACTTTGA[C/T]GCCCTGTTGCAAAGA | 55819 |
| rs552086671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946155 | AACCCCCTACAGTTA[C/T]GGTAAGTATGTGACC | 55819 |
| rs552089366 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179993122 | CTTAATCCAGTCTAT[C/T]GTTGTTGGACATTTG | 55819 |
| rs552113933 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180045407 | GACTTCAAGAGTGAA[C/G]CTGCAGACCTTCTCA | 55819 |
| rs552148085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946609 | CCCAGGCTGGAGTGC[A/T]GTGGTGTGATCTTGG | 55819 |
| rs552159612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179928177 | GAGTTATCTTTTGTA[C/T]ACATGGACATGCCTT | 55819 |
| rs552188882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926994 | ACTGACTGTTGGTCA[C/T]GGAAGTCTTCTGTGT | 55819 |
| rs552198021 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053763 | ATAACCTGAGAACTG[-/C]AACAAGCACGGCTAC | 55819 |
| rs552213656 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180058311 | TTCAGTGTATGTTAC[A/G]GCTGGTAAAAATGTG | 55819 |
| rs552229114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180023746 | AATAAATGGAGCAGA[A/G]GCAAATCACCCATGC | 55819 |
| rs552262313 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044879 | GAGGCATCATAATTG[C/G]CACCAGCACAGAAGC | 55819 |
| rs552272275 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:180058330 | GGTAAAAATGTGTGC[C/T]AATTTTTAAAAATCT | 55819 |
| rs552275796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009955 | TACACATAACAACTT[A/G]AAAGTATCTTGGCCG | 55819 |
| rs552291619 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072843 | TGGGGAGCCCCTGCT[C/T]TAGTGACTAGGTGAA | 55819 |
| rs552298608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928850 | TAGCCAGGATGGTCT[A/C]AATCTCCTGATCTCG | 55819 |
| rs552305770 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064566 | TGTCACTAATTAGGA[C/T]TGTGTGTTCACTTAC | 55819 |
| rs552314229 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949567 | AAGTTTGTCCAAGAA[C/G]GGTTTAAAACTCTGA | 55819 |
| rs552316046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179947805 | TTGATATAGCATATA[C/T]ATACTGCATATGGTA | 55819 |
| rs552335408 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929414 | TTTATTATTCTTCAA[A/C]ATGTTCTTGTTATTC | 55819 |
| rs552340149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992544 | AAACTTATCTTACTT[A/G]ACATTTTGAGGATTT | 55819 |
| rs552366656 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955328 | TAGGAGCCAATGTGA[A/G]GACACCAATAGTAAG | 55819 |
| rs552367840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053473 | ACACAAGACAAATTA[A/C]GCTTTAAGGAGGACT | 55819 |
| rs552367999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059943 | AACAAGGTTGATCAT[C/T]GGCTGACTTTACAAT | 55819 |
| rs552373883 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922704 | GCACTTTGGGAGGCT[C/G]AGCCAGATGGCTTCA | 55819 |
| rs552374912 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF130 | GRCh38.p7 | 5:179957916 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 55819 |
| rs552404835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054334 | TAGGCACTTTGCATT[A/G]TATCACCAAATGCAA | 55819 |
| rs552406179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974232 | TCAGACATCTGCAGC[A/G]GCCGGCCCCCCGCTT | 55819 |
| rs552414313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968432 | GCACTGTGGGAGGCC[A/G]AGAAGGGCAGATCAC | 55819 |
| rs552451636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008750 | TTAGCCGGACACGGT[A/G]GCATGCGCCTGTAAT | 55819 |
| rs552458984 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981177 | TGTAAAGAACAGGTA[C/T]GTGAAGAAAACTAAG | 55819 |
| rs552460424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957185 | GGGAGGCTGAGGTGG[C/G]TGGATCACCTGAGGT | 55819 |
| rs552476457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922256 | GTATCTTCGTTTGTG[A/G]AGTGTTTTGTTCAAA | 55819 |
| rs552505408 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974470 | CCATGCCAACTGCCA[A/T]CTGTCCACAGTAAAT | 55819 |
| rs552508083 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072405 | AAGAAATGTTTAAAA[C/T]TAAATGTCATGAGAT | 55819 |
| rs552508204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023007 | CCTTCAAATCTGTTA[C/T]TTACATTAAAGAATT | 55819 |
| rs552521979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179930218 | ATCTGCCACCACACC[C/T]GGCTAATTTTTGTAT | 55819 |
| rs552522169 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068503 | ACACTTGTTTATAAG[A/G]TATCTCATAAAGTAT | 55819 |
| rs552529597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179962955 | TTAGACTTATTTTCT[C/T]TTCCTCCTCACAGCT | 55819 |
| rs552550601 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180060803 | AAAGCTATGTTCGGC[C/T]GGGCGCCTGTAATCC | 55819 |
| rs552580905 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179967714 | CAGGCAGCACATGAG[A/C]AGCACAGCTGGGAGG | 55819 |
| rs552603443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964430 | CCAATCTGACTTGCT[A/G]AAAAGTCTTAACTAT | 55819 |
| rs552606951 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928038 | TTCCTTCCTTTTCAC[A/C]GCCGCATCATGTTCC | 55819 |
| rs552653898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979460 | TGCTTAAATATTAGA[A/C]TTGGGTGTGGGGCAG | 55819 |
| rs552654018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973747 | TGAAAAGAAGTTCCC[C/T]ACTCACGTGATAAAA | 55819 |
| rs552724394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056210 | ATTTATTCCCGCTGT[A/T]ACTCTTAGCCTAAGT | 55819 |
| rs552755323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009547 | TGTTACTACACAACT[C/T]AACAATCACAAGAGA | 55819 |
| rs552771958 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994822 | GCCAGCAGGTGGTAG[C/T]TGCAGGTCACAGCTG | 55819 |
| rs552774144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180019005 | TAAGCATTTTTACTA[C/T]TGGTTACTCACAGTG | 55819 |
| rs552779089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179958739 | TCACCCAGGCTGGAG[C/T]GCAATGGGGCGATCT | 55819 |
| rs552792890 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023160 | CATGTGGCAATATAT[C/T]AGAATTGGAGACATA | 55819 |
| rs552809106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964749 | TTCCGGTCCAGAGAG[C/T]GCTCTAGGAGCATTT | 55819 |
| rs552841628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179924248 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTAA | 55819 |
| rs552867655 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950412 | GTGAGCCACCCCACC[C/T]GGCCTAAATAACTGC | 55819 |
| rs552918534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974905 | GCACCCGGGTCAGCA[C/T]GCTGAGGGAATTAAA | 55819 |
| rs552940838 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179923471 | AAGTTCGGCCTAAAG[A/G]TTTCTCCATACACAG | 55819 |
| rs552947505 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982034 | TACCACATCCCCAAA[A/C]TTCTTTGTGCCCCTT | 55819 |
| rs552979854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969950 | GAGCCAAGATCGTGC[C/T]ATTGTACTCCAGCTT | 55819 |
| rs553060414 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946497 | GATAATTTCTACAAA[C/G/T]GTACTAGCGTTCTTC | 55819 |
| rs553079446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010333 | ACTCTAGAGGTTACA[G/T]ACTATATGATTCCAC | 55819 |
| rs553101758 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053941 | TTCAAGCGATTCTCC[C/T]GCTTTAGCCTCCCGA | 55819 |
| rs553137643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976490 | TTCTCCTGATTTGCA[C/T]TGGCGTGTGCATTTC | 55819 |
| rs553172574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179940154 | GCTGTGCTTAACAGA[C/T]GGTTGGAATGGGCAA | 55819 |
| rs553184034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041897 | CCCTGGGCGACAAAG[C/T]GAAACAAAAAATACA | 55819 |
| rs553225018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179951792 | AAATTTATGAACACA[C/T]AGGATTCAAACAACA | 55819 |
| rs553239616 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948142 | GGCAAGAAACTTGAA[C/T]CTTTTGAACCATCAG | 55819 |
| rs553274996 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018417 | ACCTCTTCACAGGGC[A/G]GCAGGAGAGAGAACG | 55819 |
| rs553350696 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966224 | TTCATAACTAGCTCA[A/C]GGTATTTTTTTTTCA | 55819 |
| rs553352058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985874 | TATTAAAAATCCGTT[C/T]ACAAAAATAACCTTT | 55819 |
| rs553352308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986421 | GCACTTCATACAGGT[C/G]CCATGGTGTAATATT | 55819 |
| rs553408864 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180069171 | TCATATAAACCCATA[A/G]GTTTAGAAACTACTG | 55819 |
| rs553440701 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060974 | CGCGGGAGGCTGAGG[A/C]AGGAGAATGGCGTGA | 55819 |
| rs553447229 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980376 | AAGATTCAGCATTCT[C/G]GTTGAAAAGTAAAAA | 55819 |
| rs553493793 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180027623 | CTATAACCACTGTCC[C/T]TCTCATCCTGAGCAC | 55819 |
| rs553496924 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992508 | ATTTCATTTCCAGGA[C/G]TTGTCTGTTTTTAAA | 55819 |
| rs553500850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925374 | GGATAGCTAAACACG[C/T]AGAGGTACCGGTAGG | 55819 |
| rs553504014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028212 | GGCATTCCTCTCTGA[C/T]CCCTTGGACCTAAGT | 55819 |
| rs553517163 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971417 | CTCTGTCGCCCAGGC[G/T]GAAGTGCAGTCGTGC | 55819 |
| rs553520262 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942806 | TAGAACATCCTCTGC[A/G]AATTTGCTGCTATGG | 55819 |
| rs553523721 | snp | C/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180074115 | GTGGCTTTCTCAACC[C/T]TTCTGAATTTGTCAA | 55819 |
| rs553526112 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179979708 | GGGATGACCCTGACA[C/T]ACTTTGCTCTTCTTT | 55819 |
| rs553575256 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179932412 | ACAGACATGCGCCAC[C/T]ACTCCCGGCTGATTT | 55819 |
| rs553578775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965435 | AGGTGATTAATTTGG[C/T]ATATGAAGTAACTTT | 55819 |
| rs553607935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062961 | ACTGTAAAGAAGACA[C/T]AGAAGCCCTGGGAAC | 55819 |
| rs553608497 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072559 | GACGGGTTTCCAGGA[A/G]GAGAGTTTTTCCAGG | 55819 |
| rs553630047 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180032161 | CTTATCTTTTCATTG[-/T]TTTTTCAATGGTTTC | 55819 |
| rs553653874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050627 | TTCTGTGTTCCATTT[C/T]CCTCCTCCTTATTCT | 55819 |
| rs553662799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973882 | GAGCGCCAACAAAGT[C/T]CTTTATTCCTATGAG | 55819 |
| rs553664140 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042080 | AGTATTAATTGTAGT[A/G]GATAAAGAGATGACG | 55819 |
| rs553692594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948553 | GCAGGCGCCTGTAAT[C/G]CCAGCTACTCAGGAG | 55819 |
| rs553697394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921911 | CCTGTAATCCAGCTA[A/C]TCGGGAGGCTGAGGC | 55819 |
| rs553723854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960363 | AATGTATAATCAGTC[A/G]CAGTACTAAATAAAC | 55819 |
| rs553736687 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027203 | TCTGGGGTGGGGTGG[A/G]GGGAGGATCCTGGAA | 55819 |
| rs553744374 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056046 | CTGAGATGGTGTCAC[C/T]GTACTCTGGCCTGGG | 55819 |
| rs553768668 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179942565 | ACCTTGAGTAAGAAA[G/T]AATTTTAGACATTTT | 55819 |
| rs553808722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180048110 | ACCCAGTTTCTAATA[A/G]ACACAGCTAAATCAG | 55819 |
| rs553833894 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932448 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATAT | 55819 |
| rs553844913 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000684 | TTTGCTGCTGAAATT[A/C]TCCACTGTATGTTTT | 55819 |
| rs553863507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040345 | AAATGGCAATACTAA[C/T]AGGATTATGTTGGAA | 55819 |
| rs553893187 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179994327 | ATTTTCACAATATTG[A/G]TTCTTCCTATCCATG | 55819 |
| rs553917815 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179930270 | ACCACGTTGGTCAGG[A/C]TGATCTCGAACTCCT | 55819 |
| rs553942841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929010 | ATTTTATGGTTAGGG[C/G]TTTTTCAGTCCAGTT | 55819 |
| rs553944246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935469 | ATTTTATTTTCTATC[A/G]TCTGACTTTCAACAT | 55819 |
| rs553966196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949818 | GTAAATAATTAAGAC[C/T]AGAGATGAGACCCCT | 55819 |
| rs553971823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180032531 | ATGAGCCACGAGGCC[C/T]GGCTTCTTTTTTTAA | 55819 |
| rs553983094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936418 | TTTTTTTGTAGAGAC[A/G]GGTTCTCATCATGTT | 55819 |
| rs554032933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033432 | AGCATATAGAAATAC[A/C]ATGGCTTTTGGGCAG | 55819 |
| rs554038784 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021855 | GTCCATCCAAGCTTC[C/T]GCGACTTTCCCAATA | 55819 |
| rs554039183 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937679 | CTAGAATTCTATGAC[A/C]CAGCAATTCCACTGC | 55819 |
| rs554057805 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053340 | GAAGTGACAAGTCAC[A/G]TGGAAGAAAGCAACG | 55819 |
| rs554077618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929967 | GTATAAAAGCCTTGC[A/G]TATCTTCTCTTACAT | 55819 |
| rs554077814 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061680 | ATCTTTTCCTCTTCT[C/T]ATAAGGACATTAGTC | 55819 |
| rs554086210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179922373 | GCTGGTGTGCAATGG[C/T]GCCATCTCGGCTCAC | 55819 |
| rs554095333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059619 | CTGACCTTTAAGGAG[C/T]CATAGAAAAGAAATG | 55819 |
| rs554104465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012867 | TCTAGGTGATCACAA[C/T]AAATTTAGTACCTTT | 55819 |
| rs554112132 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073704 | TTATTTACTTATCCT[C/T]GGCAAGTACAGACCC | 55819 |
| rs554125699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963061 | GACCACAGGCACGGC[C/T]GCCGGGGCTTCCCCA | 55819 |
| rs554142783 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179974608 | AGGAAAGATGGACAC[A/G]AGGGTGTCCAGGCCC | 55819 |
| rs554148766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945161 | TATGAAACAGGAACG[A/G]CCACTGGAGGTGAGG | 55819 |
| rs554183082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060101 | ACACAGGCAGCTTCT[A/G]CAAGCTGAAAAAGGC | 55819 |
| rs554236333 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179956634 | TGATCCTGCTCTGTG[C/T]GGTCCTCACTGTGTG | 55819 |
| rs554237708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046604 | GTCAAAACAGGCGGC[C/T]GCACAGCACAGTGGC | 55819 |
| rs554243804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950466 | GGTTTTAGGAACAAA[A/G]ATACATGTTTAAGGT | 55819 |
| rs554261480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043682 | CAGGAGGACTTTAAA[A/G]CTCTGCTAAAGGAAT | 55819 |
| rs554266197 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072899 | GGGTTGCAGTGGGAA[C/T]CCCCCCTCCACCTTC | 55819 |
| rs554268256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995037 | CCATTTGGTCCCCCA[A/G]TAGCAGGCAGAAGCA | 55819 |
| rs554297242 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045932 | GCTGGCTTCCCCTAG[G/T]GGATCCCGTGCGGCA | 55819 |
| rs554301572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957336 | AGAACTGCTTGAACC[C/T]GGGAGGCAGAAGTTG | 55819 |
| rs554302000 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927885 | GTGAGCCACCATGCC[C/T]GGCCTAGCTTTGTCT | 55819 |
| rs554308776 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179950474 | GAACAAAAATACATG[-/TT]TAAGGTGCAAATGCA | 55819 |
| rs554309361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944602 | CCTTGCAAGCCACCA[C/T]GCCTGGCTAAATTTT | 55819 |
| rs554309726 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180014503 | ATTTGAATTTGAATA[A/C]GGTTTGTACATATCA | 55819 |
| rs554358717 | in-del | -/GTT | 0.000115795 | 0.00760817 | cds-indel, intron-variant | RNF130 | GRCh38.p7 | 5:179955642 | TCAGTCAGAAAGCAG[-/GTT]TTTTCTTCTTCAAAA | 55819 |
| rs554367641 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953479 | CATAAACTCATATGT[C/G]ATTCTCAATTGATTT | 55819 |
| rs554371985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035396 | AGTCTTTGAAAATAT[A/G]TTCAGACTTGATTTA | 55819 |
| rs554384719 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979826 | AAAAAATAAAACAAC[-/AA]AAGAGACATAGCAAA | 55819 |
| rs554389771 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179952709 | CAATGTAATGCACCA[C/T]ATTCATAGGATAGAA | 55819 |
| rs554404372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998352 | GGTTGTTTAGGAGCA[C/T]GTTTGTAAATTTCCA | 55819 |
| rs554405885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988103 | CTGGTCCTGAGTTTT[C/T]GTTGAGGGATCATTA | 55819 |
| rs554418316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980708 | GTCACAGCTCCACTT[C/T]TGGCTCGCTATACTA | 55819 |
| rs554440602 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948962 | CTTCCTTGGAATAAT[-/T]TTTTTTTTTTTTTTT | 55819 |
| rs554448264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025615 | AGTGTTTCAGTTTTA[C/G]ATTTTGATAATTATG | 55819 |
| rs554479539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981264 | GAACACTCACACTGG[G/T]ACAAGGGGCAAAAAC | 55819 |
| rs554482253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179941693 | TTTTCTCCTCAAGTC[A/G]TCACTGCACTGATAG | 55819 |
| rs554504947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071012 | ACCACTTAAGAAAAA[A/C]GGCACGTTTTTATAT | 55819 |
| rs554509776 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180004687 | GGCTTAATCTAATAG[C/G]AATAGTTGGTTCAAA | 55819 |
| rs554512482 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027704 | TCTTCCTCTCCACAC[C/G]TCACCTGTGGGGCTT | 55819 |
| rs554519888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057286 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs554544310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929931 | TCTTTAATTTCTCTC[A/G]ATAACACATAATTGT | 55819 |
| rs554559526 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072583 | TTCCAGGGACTGAGG[A/G]AGTTGAAGTGGTTTC | 55819 |
| rs554571739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180029151 | ATTTTAGAGGTACTA[C/T]ATCATCCAACTAAAA | 55819 |
| rs554573629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062856 | GATTCTCAATCTGTC[A/C]CGTTAACTGGCCATT | 55819 |
| rs554630587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959537 | GAAGACTGAGGCAGA[C/T]AATTTCTTGAACCCG | 55819 |
| rs554635422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966140 | CAGCTCACTCACACC[A/G]TCCTGAGGCACCGCC | 55819 |
| rs554637178 | snp | C/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955548 | TATGAAAAAATAAAA[C/T]GTACTAAAAATAAAT | 55819 |
| rs554637265 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073395 | CTACTAAAAATAAAA[A/G]AATTAGTCGTGGTGA | 55819 |
| rs554638194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952795 | AATCAAAAACTATTT[A/C]ATGATAAAAACGTTC | 55819 |
| rs554644742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977386 | GCTTGGAGATGTAGT[C/T]TAAGATGGAGAGGAA | 55819 |
| rs554647006 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021239 | ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 55819 |
| rs554677131 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021391 | ATGTATAAAATACCA[A/T]CAACCACAAGGTACA | 55819 |
| rs554694340 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179960271 | CCTTGCATTTATTCA[C/G]TTCTTTGACTACCAT | 55819 |
| rs554694508 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978917 | AGAAGGGGTTTTGCA[A/G]AAGTTGTCATAAAAC | 55819 |
| rs554704077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179972835 | CCTGTTTCTTTAACC[C/T]GAAATTAGTTATAAA | 55819 |
| rs554732367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180030634 | TGCCTCAGTCTCCGA[C/T]GTAGCTGGGATTACT | 55819 |
| rs554769745 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179938662 | TATATATTTAAATAA[-/T]TGTCAAAATTAAGTT | 55819 |
| rs554772843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961797 | CTACTATGGTACTGT[A/G]TCCCACTTCACAGAA | 55819 |
| rs554812000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976772 | AGACCAGTAGCCTCA[G/T]GGAGATAACAACTCA | 55819 |
| rs554837365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058472 | GGAACTAACCTAGTC[A/G]AATTCATAGAGACAG | 55819 |
| rs554840923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028555 | TGAAGTCTTCCAGAC[C/T]TGGGTCAGAACCCCT | 55819 |
| rs554849980 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052904 | AAAAACCTTAAAGTT[C/T]ACCTTAAATATAGAA | 55819 |
| rs554892526 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009347 | ATCTCTGCAAGCCAC[A/G]TATTTGACGAAGGAC | 55819 |
| rs554904845 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073522 | CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 55819 |
| rs554957495 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954893 | AAGCATATAATTCGA[C/T]GTAACAAAGTATTTT | 55819 |
| rs554968014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948067 | AAGTAGTTGGGAGCA[C/T]TGACTCTGGGCTGCC | 55819 |
| rs554988517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066947 | GGAGGATCAATCACT[C/T]AACTCCCCGAGGTCA | 55819 |
| rs554998802 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179969143 | CATTCTTTTTTGAGA[A/C]CAGAAACTATGTTAT | 55819 |
| rs555000713 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057947 | GGTTTTGTGGGACTA[C/G]GCCCTTTACCTGTGG | 55819 |
| rs555025237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022105 | GCGCTCTTTTCAGTG[A/T]ACACCACCAGGCGGC | 55819 |
| rs555027810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180067559 | ATATTTATAGGCTAA[C/T]GGAAATCATCATTCA | 55819 |
| rs555037581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179973495 | CTCAGCTAAGGACTG[A/G]GCCAGGGGCGTTTAA | 55819 |
| rs555052282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179925059 | AGTGTATTTGGTTTT[C/T]ATCCGGGCTTCCTGG | 55819 |
| rs555077313 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180013993 | TGAGTGGAGTTGAGG[A/C]TCCTTGCTAGTTTAC | 55819 |
| rs555078621 | in-del | -/CCCCGCCC | 0.00755907 | 0.0610114 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072141 | GCGTGTCCGCCGCCG[-/CCCCGCCC]CCCCGCCCCCCCGCT | 55819 |
| rs555105787 | in-del | -/GGTGCCTGCCTGTAATCCCAATCCCAGCTACTC | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179931634 | TTAGCCGGGCGTGGT[lengthTooLong]GGTGCCTGCCTGTAA | 55819 |
| rs555123193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974843 | CAGGCACGCAGCGGC[A/G]CGGGGAGGAGCGGCA | 55819 |
| rs555140700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006400 | ATATATTTCCACATT[C/T]TGACAGGCAAATGCA | 55819 |
| rs555140825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014364 | TCCTTTCATAAGCTG[A/C]AGCTGCCGGTGGCAA | 55819 |
| rs555151748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060199 | CCAGTAAAACTCATT[C/T]CAGAATTCTGACCCC | 55819 |
| rs555157099 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976922 | TTCCTATTTATCCAA[C/T]TGATACTCAGAACTG | 55819 |
| rs555189216 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000261 | GTAAGATTTCTCTGG[-/A]AAAAATCTGTTTTTA | 55819 |
| rs555198760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930207 | GGATTACAGGCATCT[A/G]CCACCACACCCGGCT | 55819 |
| rs555213554 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023739 | ATAAATTAATAAATG[C/G]AGCAGAGGCAAATCA | 55819 |
| rs555240355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052898 | ATAAGAAAAAACCTT[A/G]AAGTTCACCTTAAAT | 55819 |
| rs555278021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179996078 | ATTTTCACAATATTA[A/G]TTATTCCTATCCATG | 55819 |
| rs555295279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937586 | GTAGCAAATCAGAAC[C/T]CTTATACATTGTTGG | 55819 |
| rs555297157 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959651 | AAAAGAGTACTGAGC[-/A]AAATAATTCAGAAAT | 55819 |
| rs555299135 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985451 | CCCCTGCTCTAGAGG[C/T]TGAATTAGAGGCATG | 55819 |
| rs555318365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045586 | CCCTTATCTGACCCC[A/G]CCCACATCCTAATTG | 55819 |
| rs555321825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980493 | TGCTGCATTTTGTGT[C/T]GAATAAACATTTGAA | 55819 |
| rs555331680 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988970 | GTCCAATGTTGACAG[A/C/T]GGGTGTATTAGTCCG | 55819 |
| rs555351958 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989703 | TATCTTTTAAGCGGA[A/G/T]CATTTGATCCATTTA | 55819 |
| rs555373451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024772 | ACATAAAAGCCTACC[A/G]TTTTTTCATGAGTTT | 55819 |
| rs555407252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981825 | CTGCTCCGTCTTTGA[A/C]GCCTAATCTATGAGT | 55819 |
| rs555411020 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180003713 | AATTTTTCATTCTAA[C/G]TCTATTTGCATCCGG | 55819 |
| rs555439533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951580 | AGTAGAGACGGGGTT[A/T]CACCGTGTTGGCCAG | 55819 |
| rs555528637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923060 | AAATTTTGGTAAGAT[A/C]AAATTTATTGATTTT | 55819 |
| rs555544369 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180055715 | ACAAATGCCTTTTTT[A/T]AAAAACCCCAGCAAA | 55819 |
| rs555546695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018022 | AGGTTCAGGCTGGGC[A/G]TGGTGGTTCACACCT | 55819 |
| rs555563037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180010181 | GAACCTGGGAGGCGG[A/G]GCTTGCAGTAAGCTG | 55819 |
| rs555586974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034581 | ACAATCTGTATATTT[C/T]TAGGAATTTGTTCAT | 55819 |
| rs555615639 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988787 | AAAATTTGTTGAGAC[G/T]TGTTTTGTGGTCTAA | 55819 |
| rs555624860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019923 | TCTCGGACCCAGTGA[A/C]ACTGTTGGGCAAAGT | 55819 |
| rs555652172 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180027486 | GCCTGGCTGAAAAGA[C/T]GAGACTCAGAGAAGC | 55819 |
| rs555653311 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180032695 | CCACTGATCTATATG[-/C]CTGTCCTTCTACCAA | 55819 |
| rs555660051 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961935 | TTATGTACCAGGCAC[G/T]GTGCTAAGCATTTTA | 55819 |
| rs555695413 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180047699 | CAGTGAGCCGAGATT[A/G]CACCACTCCACTCCA | 55819 |
| rs555730516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048315 | CGGCAAATCACTCTG[A/T]ATCTAATTTGTCTGT | 55819 |
| rs555739447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971365 | TGGGATAAGATAAAA[G/T]AAATTTTTGTTTGTT | 55819 |
| rs555762918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945304 | GGGAAAACAGTGGGA[C/T]CCAATGGACCCAAAC | 55819 |
| rs555774131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931566 | CTGAGGTCAGGAGTT[C/T]GGGACCAGCCTGGCC | 55819 |
| rs555802818 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933707 | TTTCTACTTTTTGTA[A/G]AGATGGAATTTCACC | 55819 |
| rs555822888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034061 | ACAGATGCCCTTTAT[C/T]AGGCTGAGGATATTT | 55819 |
| rs555828616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180041842 | AGCACTTTGGGAAGC[C/T]GAGGCAGGTAGATTG | 55819 |
| rs555873445 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179945755 | GCGGTGTCCGGCCTC[A/G]GCAGGAACCTAAATA | 55819 |
| rs555905185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975272 | GAGTGGCATCTGCTG[A/G]GGTGAGGCTTGAAGA | 55819 |
| rs555909894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022336 | TACAGATTCATGGTT[C/T]CTATTTTATTCAATC | 55819 |
| rs555934666 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939604 | GAAGTTGATATAGAT[G/T]TGAAGTTGCCATTCC | 55819 |
| rs555941599 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053779 | AACAAGCACGGCTAC[A/G]TGACACTGACAATGA | 55819 |
| rs555947106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940064 | TCTGGGTGCCACATC[A/G]GTGTCATTCTCCAAC | 55819 |
| rs555959249 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180068358 | CATAAATACAAGACA[C/T]GTTCCTTCAAAACTC | 55819 |
| rs555960334 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936290 | AATTTTTTGTAGAGA[C/T]AGGGTCTTGCTATGT | 55819 |
| rs555992312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030284 | AGAATACTTGAGGAC[A/C]TACAACTGAAACCTG | 55819 |
| rs556034883 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179970694 | CCTGAGCCCAACCTC[A/G]TATGTACAACACCGT | 55819 |
| rs556037313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934652 | GGGTTCAAGTGATCC[A/T]GCTGCCTCAGCCTCC | 55819 |
| rs556040820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069081 | AACACGAATAATTTT[A/C]ACAGATTTATATCAC | 55819 |
| rs556087223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015095 | GCCACTTTATTAGAA[A/C]AGCAGTTTACCAGAA | 55819 |
| rs556103191 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179921707 | GAGGCTGAGGCAGGA[A/G]AATCGCTTGAACCCA | 55819 |
| rs556118510 | in-del | -/ACA | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179970700 | CCCAACCTCATATGT[-/ACA]ACACCGTGTAAGAAC | 55819 |
| rs556140401 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002417 | AAGGGGAGCCATGAC[C/T]ACTCACCCCTGGAGC | 55819 |
| rs556144187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922282 | TCAAATCTTTAGTCC[A/G]TTAAAAAAACTGGGC | 55819 |
| rs556146087 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053099 | AAGCTAAATTAGACT[G/T]CGATGCGGGAGCATG | 55819 |
| rs556168053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180065536 | GAGGCCGAGACAGGC[A/G]GATCATGAGGTCAGG | 55819 |
| rs556174494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927538 | TGTCCTCTCTCCCCC[A/G]CCAAAGGAAACCATA | 55819 |
| rs556227266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044930 | ACGAAGTGCACTTAA[C/G]AGACTGAAGGAGGGA | 55819 |
| rs556254024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180049862 | TTGACCGAATTTCAT[C/T]TCCCCCTTTTCCTCA | 55819 |
| rs556254190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059093 | CACTGACTTTTTCAA[C/G]TCTACTGTGCCCCAC | 55819 |
| rs556291752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179947962 | TCCATTCACTTCCCC[C/T]GTTTTCACCCTGAGA | 55819 |
| rs556294267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030954 | CCATCCCTGAAATAA[A/C]AAGACCAACCGTCCT | 55819 |
| rs556307030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000875 | CTGGCAATTCATTAA[C/G]TTTTTTCCCATTGGA | 55819 |
| rs556311272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962435 | AGGTAATCAGTTTGG[C/T]TATTACTCATCAATT | 55819 |
| rs556353144 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071923 | CCTCGGCGAGGGCGG[A/C]GTCTCAGGTCGCACG | 55819 |
| rs556356801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046511 | GTAGGCTAAGGGTTT[C/G]CTTCCTACCCCTGAG | 55819 |
| rs556365888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978673 | GGAAGCTCACCAGGA[C/T]GTTCACTTAAACACA | 55819 |
| rs556370069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064800 | CTGTAACTAGAATTA[A/G]GTCTTCCATGCTTTA | 55819 |
| rs556372610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955909 | ATGAAGGAAAAGGTC[A/G]GGCCCATGGCGTGTT | 55819 |
| rs556397493 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009479 | TATACGGATGGCAAA[C/T]AAGCACATAAAAAAT | 55819 |
| rs556413203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179935254 | ATTAGTTGAAATTTG[C/T]TAAATTTATTGAAAT | 55819 |
| rs556432102 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031353 | TTAGCTGGGCATGGT[A/G]GCACGCACCTGTAAT | 55819 |
| rs556433773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040305 | GAAATTCAACTATGG[G/T]GAAAAAACATGCATC | 55819 |
| rs556439918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179944032 | GCTGGAGTGCAACGG[C/T]GCGATCTTGGCTCAC | 55819 |
| rs556442869 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072499 | GACACGAGTGGTTGG[A/G]AAAGACCTCTAGGGT | 55819 |
| rs556450980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973799 | GCCCGCCACACACAG[A/G]GTGGGTGGTGCATCG | 55819 |
| rs556484143 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062815 | GGGACTTGACTTGTT[A/G]ACTACTAATGGCCAT | 55819 |
| rs556512366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179968164 | GCCGGGCATGGTGGC[A/G]GGTGCCTGTACTCCC | 55819 |
| rs556525607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059593 | TAACATGCAAATGAG[A/G]AGGTGCATCACTGAC | 55819 |
| rs556542531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925241 | CACCCCCCAGCCTCC[A/G]GGGAGCGGAGAGGGG | 55819 |
| rs556580574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962992 | ACATCTGGAAACAGC[A/G]GGTCTTTCAAACTGC | 55819 |
| rs556592343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936697 | AAACAAAGCTGGAAG[A/G]CTCAAACTTCCCAAT | 55819 |
| rs556602773 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956576 | TGTCTCCTGCCTACC[A/G]TCACCACCACCTACA | 55819 |
| rs556629930 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069740 | TGTCACACAATGGAC[A/G]TAAAGCACAGGCCTG | 55819 |
| rs556640643 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179968508 | CCATCTCTACTAAAA[A/G]CACAAAAATTAGCCA | 55819 |
| rs556666212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180049565 | ACTGTACAAGTATTA[A/C]CATGTCACAGACATG | 55819 |
| rs556715798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932984 | AATGACCATTATCAG[A/G]AATGAAAAAGACATC | 55819 |
| rs556738922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965337 | CTACGGTGCCCAGGG[C/T]TTCGGAGGGAAAGCA | 55819 |
| rs556750493 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959122 | AACCAGGCAATACGG[G/T]TAAAAGAGACCAGTG | 55819 |
| rs556774291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952725 | ATTCATAGGATAGAA[A/T]AGAATAAAGGGCAAA | 55819 |
| rs556788160 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941156 | CTATTTCTGTTCTTT[A/G]TTTTTTCTCCTTTTT | 55819 |
| rs556799703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179987273 | CCTGGGCTCAATCCA[G/T]CCTCCTGCCTCAGCC | 55819 |
| rs556803816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994954 | TGGGTCTTACACTCA[C/G]CCTTGGGGGAGGGGA | 55819 |
| rs556804454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179959432 | GGAGTTCAAGACCAG[C/T]CTGGCCAAGACAGTG | 55819 |
| rs556833348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953249 | ACAATATTGTTGAGA[C/T]AGCAATGCTAACTAA | 55819 |
| rs556835613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946532 | TCTTAACAGACCGAC[A/C]AGTACAGCACACCCA | 55819 |
| rs556845902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946689 | CTCCCGAGTAGCTGG[A/G]ACTACAGGCGCCCGC | 55819 |
| rs556887232 | snp | C/G | 0.0114733 | 0.0748667 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920276 | GATCAGAAATCAAAT[C/G]ACAAAAGCAGTGACC | 55819 |
| rs556908845 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948014 | AGGCTGTGCACATAG[G/T]AGGTCCTGGTCTAAC | 55819 |
| rs556938315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003821 | CTAAACACCATGCCA[C/T]TAAGTCACTGTTTTT | 55819 |
| rs556966748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964812 | CTTAGTAAACCCCTA[C/T]CTTTTAGACACCAGT | 55819 |
| rs556972323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043632 | AAGACACAGCAAGGG[G/T]TGCAACCACAGAGCA | 55819 |
| rs556979867 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958839 | GTACCTGCCACCACA[C/G]CCAGCTAATTTTCAT | 55819 |
| rs557007107 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972091 | CAGATACATTCAGTA[A/C]ACCTAAGGCGTTATG | 55819 |
| rs557015310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180070870 | GGCTAGTAGTTCCGA[C/T]TAGTGTCAGATCCTC | 55819 |
| rs557045515 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940628 | ATAAAGTATCTTTTT[C/T]TCTGCCTTTAAGTTT | 55819 |
| rs557076054 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941984 | TCCTATTTGCTGTTT[C/T]ATGTCTTTCTTTCTC | 55819 |
| rs557112445 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967530 | AAAGACTTTTGAACT[A/G]TAAGAAAATGATCTG | 55819 |
| rs557117503 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972659 | GCCGCAGCACCACCT[A/C/G]GGGGGATGGAGGTGC | 55819 |
| rs557187832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179997448 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55819 |
| rs557188947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982953 | ATGTACTTATTGGCC[A/G]TGTGTACATTGTCTG | 55819 |
| rs557199949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990454 | AACATGAGAGCGGAC[A/C]AGGGGCGTGACCGCT | 55819 |
| rs557217443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034812 | GAGTCACTGAACCTG[C/T]GGATGGTCATGGGGA | 55819 |
| rs557231161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013829 | TGTCTGTAGAACTAG[C/T]GCCAGGAACAAAAAC | 55819 |
| rs557241738 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946597 | CTCGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 55819 |
| rs557253714 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041596 | GGTTCAAATGAGAGA[A/G]AAGGGCAGCCCAGAA | 55819 |
| rs557259788 | in-del | -/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180028049 | CTATTACCCTATCCA[-/C]CCATGTTGAGCTGTG | 55819 |
| rs557274816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179931688 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 55819 |
| rs557278165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057931 | GTCTGAAGTAGGGGG[C/T]GGTTTTGTGGGACTA | 55819 |
| rs557288684 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035971 | TCTTTGGACATATTT[A/C]TATTAATTGCTTTGA | 55819 |
| rs557290643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006262 | GACAAATCTTGGCAG[C/T]ATATACAATACTTCC | 55819 |
| rs557300144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180027670 | CCTAGCAGCCAGGAC[A/G]CGTGCCTTCCTGCTC | 55819 |
| rs557302076 | in-del | -/TTA | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179992730 | TTTTTTATGGTTTAT[-/TTA]TTATTATTATACTTT | 55819 |
| rs557303411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976062 | ACGTCAGGCTCATGC[C/T]TGTGATCCCAGCACT | 55819 |
| rs557322868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990972 | AATATTGGAATAGCT[C/T]GTGCCCTCGGTCTCT | 55819 |
| rs557328040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179979196 | GTCACCGTGGTCACC[A/G]CTCCTCTGCCATTGA | 55819 |
| rs557338698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979869 | TATAGGAAGAAAACA[C/T]ATCTCCTGGCTTTTT | 55819 |
| rs557367379 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028432 | CTCCCTCTCCTCTCA[A/C]CAGATTTTTGATTCA | 55819 |
| rs557392453 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179954436 | ACAACATGTATGAAC[C/T]GTGAACACATGCTAA | 55819 |
| rs557393885 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037608 | TTAATAATACAGGCT[C/T]TTGGGTCATATTCCA | 55819 |
| rs557425087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935714 | TTACAGTTTTCTCTC[C/T]ATTAGTGTATTATAT | 55819 |
| rs557452193 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965380 | GTTTAGTTCAATCAC[A/C/G]TGGGTTTTATTTATT | 55819 |
| rs557458442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933213 | TAAAAAGAATTCACC[A/G]ATGAAATCATCTAGG | 55819 |
| rs557473050 | snp | A/C/G | 4.94281e-05 | 0.00497112 | missense | RNF130 | GRCh38.p7 | 5:180013128 | ATGAGCCATGCTGAA[A/C/G]AAATAATCATCAAAA | 55819 |
| rs557477561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028981 | CATTACAGTTTGTTA[A/G]CTCAATAAATTTTGC | 55819 |
| rs557479466 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997835 | TTCTTCTGACTTTGG[G/T]TTTGCTTTGTTTTCA | 55819 |
| rs557497506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057537 | TGGGTGACAGAGCGA[A/G]ACTCAGTCTCAAAAA | 55819 |
| rs557516394 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992915 | GTGTGTGATGTTCCC[C/T]ATCCTGTGTCCAAGT | 55819 |
| rs557538869 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180021455 | GCAACTCTAAGATGT[C/G]ATGGAATACAAGAAA | 55819 |
| rs557548105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066277 | CAGGGGTTTCCACTT[C/T]TGCATCTTCCTAATT | 55819 |
| rs557556412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179926541 | GTAATCCCAGTTACT[C/T]GGGAGGCTGAGCAGG | 55819 |
| rs557574780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180038059 | TTTTTTGTTTAGTTT[C/T]GTGTTTGTCTTTGAG | 55819 |
| rs557578875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960381 | GTACTAAATAAACAG[C/T]ATTTCATCATAACAG | 55819 |
| rs557593679 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920017 | AGAGATGCGTCTGCA[A/G]TGCAACATTAATCCT | 55819 |
| rs557623783 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058408 | ATGCTACAACACAGA[A/T]GAACCTGAGGACATA | 55819 |
| rs557625335 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009167 | TTCCAGGAAAAATAG[A/T]AGAAAATCTTTGGGA | 55819 |
| rs557628420 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062202 | TGGGACTACAGGCAC[A/C/G]CACAGCCACGCCTAG | 55819 |
| rs557649642 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179968686 | AAAAAAAAAAAAAAA[A/G]AAGAGAGAAAGTTTC | 55819 |
| rs557679345 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180051522 | GATTACAGGCGTGAG[A/C]CACCGCGCCCCGGCC | 55819 |
| rs557683645 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937575 | TTGGCAAGGAGGTAG[A/C]AAATCAGAACCCTTA | 55819 |
| rs557685945 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180003140 | GGCAAGCAGCAGTAG[A/G]TAAAGAAAGAAGAGC | 55819 |
| rs557685996 | snp | A/G | 0.030278 | 0.119257 | intron-variant | RNF130 | GRCh38.p7 | 5:179995195 | AGGCAAACAGTATGG[A/G]ACCTGCCTCTCTCTC | 55819 |
| rs557698981 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990431 | GCGGAGCCAGGTGTA[C/G]AGGATGGAACATGAG | 55819 |
| rs557716079 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180051996 | TCCACATCACTCTTC[A/G]TTCCACAAAGGAATT | 55819 |
| rs557731361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987067 | CTCTTTGTTTTTTTT[C/G]TACATATGGTCACAT | 55819 |
| rs557747282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995946 | AAAAGCCTCTAATCT[C/G]CTGTCTTTGGGGGAA | 55819 |
| rs557819789 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965129 | CATCCCGTATTTGCA[G/T]GTCTTTGTGTGTGTG | 55819 |
| rs557871365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023934 | CCTCAGCCAGGTGAC[C/T]AAAGTCAACATCACT | 55819 |
| rs557885439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988201 | GGAATGTATCCATTT[A/T]CTCTAGGTTTTCCAG | 55819 |
| rs557897664 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179958036 | GCGCCCGCCACTACG[C/T]CCGGCTAATTTTTTG | 55819 |
| rs557905275 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988373 | TGTTGATCCTTTGTA[C/T]TGTGTTTTTAGTCTC | 55819 |
| rs557906628 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034987 | TTGTCAATTTTATTG[A/G]TAGTTCCAAAGAACC | 55819 |
| rs557934106 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180060137 | AATGATTCCCCCTGA[C/G]AGCTCCAAAGCCACG | 55819 |
| rs557936888 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946177 | TATGTGACCAAAGGC[A/C]CATGCTGGAAACTCA | 55819 |
| rs557952981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929865 | TGGGGAGAGCTAACA[A/C]CTCCATAGTATCGTG | 55819 |
| rs557981368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969072 | GGTTGCAAGCTAAAA[A/T]GAGTTCATCTGTTGG | 55819 |
| rs557987388 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180029445 | TAGAAGTTCAAAGGG[-/A]AAACAGAAAGTGCTC | 55819 |
| rs557987663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963682 | TGTAAGCCAAGATTG[C/G]CCCAAGGAAGTGAAG | 55819 |
| rs557992053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923008 | GTGACTTGCCTTGAC[A/G]TTGTTATAACAATGT | 55819 |
| rs558012281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009838 | TAATAGCCAAAATCT[C/G]AAAACATCCCAGATA | 55819 |
| rs558015300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026677 | ATTGGTACATACAGT[A/G]TATAGGGAATACTTA | 55819 |
| rs558042214 | in-del | -/AAAT | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179939218 | AAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 55819 |
| rs558074139 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054985 | TTTATTGATCTTTTA[A/T]CTATGGGTGTTCCTA | 55819 |
| rs558078874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019108 | ATCACTTTGAGGCCG[A/G]GCGGGGTGGCTCACG | 55819 |
| rs558103121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957445 | AAGCAAAATAATAAC[C/T]ACTGCCAAAGAGAGC | 55819 |
| rs558110986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180055648 | ACTACTCAGTTACAG[A/G]ATTTACAGACGAAAT | 55819 |
| rs558146452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999146 | TCTGCCTCAGACTCC[C/T]GAGTAGCTGGGATTA | 55819 |
| rs558161040 | in-del | -/A | 0.33303 | 0.235809 | intron-variant | RNF130 | GRCh38.p7 | 5:180065136 | CTACAGAATGAATTT[-/A]AAAAAAAAAAAAATC | 55819 |
| rs558197918 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:179930732 | AGTTTGCTAAAAGTT[A/C]TTTTCTTTTAAAATC | 55819 |
| rs558208555 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179985733 | TTTATCAATAAGGGC[A/T]GTCTTGATCATAGAC | 55819 |
| rs558239450 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | RNF130 | GRCh38.p7 | 5:179945276 | CACCCTGCAGGGTGT[A/G]CTGACTGCACCTGGG | 55819 |
| rs558241518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033515 | GGTCACTTGAGGTCA[A/G]GAGTTCGAGACCAGC | 55819 |
| rs558244354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036153 | TCTGGATTCTGATAT[A/T]TTCCCCCTTAAAGTT | 55819 |
| rs558281586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051343 | CAAGCTCTGCCTCCC[A/G]GGTTGACGCCATTCT | 55819 |
| rs558290398 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992421 | TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC | 55819 |
| rs558325049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981325 | TCACTCTAGACACAT[A/C]CAGGCCTTACACTGT | 55819 |
| rs558383267 | in-del | -/A | 0.0227342 | 0.104165 | intron-variant | RNF130 | GRCh38.p7 | 5:179939278 | AACTTTTAAGACAGA[-/A]AAAAAAGTGGTCCTA | 55819 |
| rs558392707 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974955 | AGTCAATGGTGAAGC[A/G]GTCCTCTGAGAGTGA | 55819 |
| rs558397723 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179991911 | ATTCTCATGAGGAGC[A/C]CTCAACCTAGATGCT | 55819 |
| rs558423380 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179933819 | ACTAGATAAAGAATC[C/G]CAGGATTTTCCCTCC | 55819 |
| rs558446171 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949693 | GTTGTGTGAAATTAA[A/G]TAACTCAAAGCTGTT | 55819 |
| rs558455245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926804 | GCGCTGGGCATTGGA[C/T]GTGGAGACAGTCTTG | 55819 |
| rs558481122 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006026 | ATATGAAAAGTGTTA[C/T]TTATTTACAAAATGG | 55819 |
| rs558499197 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179927511 | GTCCCTCCAGTGACC[A/G]CCCAATCACTATGTC | 55819 |
| rs558532018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058560 | TAATGGGTATGTTTT[A/T]ATTTTTTATTTTTGA | 55819 |
| rs558547708 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071732 | CCGCCGCTGCTCGCG[A/G]ACCGGGCTCCGGGGC | 55819 |
| rs558559396 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976367 | ATGGTTCTGGAGGAT[C/T]CTGGGCTGAAACAGC | 55819 |
| rs558561115 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043746 | GCATGATCAAAACAA[A/C]TCCAACAACGGCCTG | 55819 |
| rs558577444 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022268 | GTGCTTTGAGGCTAG[G/T]TAAATATTCCATCCT | 55819 |
| rs558615040 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179946719 | CCACCACGCCCGGCT[A/G]ATTTTTTTGTATTTT | 55819 |
| rs558642134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064652 | AAACCTTTCTAGCTT[C/T]GCAACTAGAAACTAT | 55819 |
| rs558646258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014426 | AGCCCCTGAGAGAGA[C/T]TAGGGGTCATTAGAA | 55819 |
| rs558653020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053026 | TGTCAAGATAATGTA[C/T]GTCCTTCAAGGAATC | 55819 |
| rs558694037 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049909 | CTATTTTTTTAGTGC[C/G]TACCCTTAAAATGTT | 55819 |
| rs558701372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951305 | ACAGAGAAGAAAAAC[A/C]AGATAAGATTTGAGC | 55819 |
| rs558716267 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012261 | CCACAGGAATTTGAA[A/T]GTACCATGTTAGGAG | 55819 |
| rs558755208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071051 | GGCCGCATCCTTCCA[A/G]ATCTAGCGCAGCCTT | 55819 |
| rs558760539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179955794 | CCCAACCCCTCTGGT[A/G]AGGCCAGGAAGCCAT | 55819 |
| rs558793758 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935124 | ACTTTTTCTTTTGGA[A/T]GTATATTGTTTAATT | 55819 |
| rs558795957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942409 | AATCTCCAAATTTTG[C/G]AAAAAAAGAATATAT | 55819 |
| rs558796359 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179977510 | AGGAGGACTGCTTGA[A/G]CCCAGGAGTTCATGT | 55819 |
| rs558804944 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965895 | AGGAGAAACATTTTG[G/T]AACAGTGTCATCCAT | 55819 |
| rs558805336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021656 | AGAATCTAAAACTTA[C/G]AGAAAAATTCGAAAT | 55819 |
| rs558818836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948688 | TCAAAAAAAGAGAGA[A/G]AGAGAAAAAAAGAGT | 55819 |
| rs558822774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996136 | CTTCAATTTCTGTCA[A/T]CAGTGTTTTAGTTTT | 55819 |
| rs558831106 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | RNF130 | GRCh38.p7 | 5:179949497 | TCTAGAAAAATACTT[A/T]AAAAAAAAAAGAAAG | 55819 |
| rs558834888 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973314 | TCCACAGGCAGCTGC[C/T]CTGAACACGGCACCT | 55819 |
| rs558865185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978017 | GAAGGCCGTGCAGCC[C/T]GCACCTGCTGAACAG | 55819 |
| rs558865473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973125 | TCCTGACCCTACCTC[C/T]GAGCACTGAACACCC | 55819 |
| rs558884180 | in-del | -/ATTC/ATTT | 0.00597694 | 0.0544006 | intron-variant | RNF130 | GRCh38.p7 | 5:179925512 | TCTGTTTTTTCATTT[-/ATTC/ATTT]ATTTATTTATTTATT | 55819 |
| rs558905881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963305 | CAATCTGTGTTACTG[A/T]CTAAAAATATATGCT | 55819 |
| rs558962774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946625 | GTGGTGTGATCTTGG[C/T]TCACTGCAAGCTCCG | 55819 |
| rs558970801 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179968154 | CAAAACATTAGCCGG[C/G]CATGGTGGCGGGTGC | 55819 |
| rs559019169 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922655 | TTTAAAAAAAATTCT[A/G]GGCCGGGCACAGTGG | 55819 |
| rs559029592 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962336 | ATGCCACTGCAAGTG[C/G]AGGCCACTTGCCCAT | 55819 |
| rs559037110 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921205 | GGCCAGTGACACCGA[A/C]ACCACCATCAAGATA | 55819 |
| rs559050658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054283 | CCTAGGATTTGCAAA[C/G]TTAAAAAATGATACA | 55819 |
| rs559055330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921549 | ATGCCTGTAATCCCA[C/G]CACTTTGGGAGGCCA | 55819 |
| rs559056855 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179923093 | CCTATTATAGTTTGT[A/G]CTTTTTGTGTCAGAT | 55819 |
| rs559070708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969235 | TCCTTGGTTACTCAA[A/G]TCAGTGTTGACCTGG | 55819 |
| rs559073217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007311 | GAGGCTGAGGCAGGA[A/G]AATTGCTTAAGCCGA | 55819 |
| rs559110505 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919964 | AAAGGATGTTAAAAA[C/T]CCCAGCTTCCCTGGT | 55819 |
| rs559110569 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947535 | GGGGGCCAGCTTATG[C/T]GTTGAAATCCAGCCT | 55819 |
| rs559134679 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007916 | CTGTCAACAACACCA[C/G]TCCAGAGCAGCTCCT | 55819 |
| rs559142499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981015 | GCGAGGCAGGGGAGG[A/T]ACGTCAGGGAAGGTC | 55819 |
| rs559148460 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180000825 | TTCTTGTATCTCTCT[C/G]AGTTTCCATACGATC | 55819 |
| rs559153068 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923822 | TTTCCCTAAAGTTTT[C/T]CTTTTAACAACACTA | 55819 |
| rs559196493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021021 | GGAGTCTCACTCTGT[C/T]GCCAGGCTGGAGTGC | 55819 |
| rs559202972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180046124 | TGTGCGCGGTGGACC[A/G]CGGCGCGTGCAGGCC | 55819 |
| rs559234512 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996281 | TGGTGTATATACACA[C/G]AACTGATTTCTGTAT | 55819 |
| rs559302370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031170 | TTATCAGTGAGGCTT[C/T]TGGTCAACAGCAAGC | 55819 |
| rs559313198 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179951399 | TTTTTGTTTTTTTTT[A/T]TTGAGATGGAGTCTC | 55819 |
| rs559320284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975045 | TGCCGAATGCGGAGC[A/G]CCAGCCAGGCGGGGA | 55819 |
| rs559332373 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179975291 | GAGGCTTGAAGAGCC[A/G]CGCACAGCCATCCTC | 55819 |
| rs559358701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002005 | CCAAGGCACCAACTC[C/T]CCAAAGGATAATGTG | 55819 |
| rs559358993 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009969 | TGAAAGTATCTTGGC[C/T]GGGCGCAGTGGCTCA | 55819 |
| rs559363056 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180046009 | TGGAGCAGGGGGCAG[C/T]GCTCGCCGGGGAGGC | 55819 |
| rs559398692 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064629 | TATGTTCATTTTCCT[C/T]TGTTTTTAAACCTTT | 55819 |
| rs559399487 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043610 | TTCATAATATTCTAA[A/G]AATGAAAAGACACAG | 55819 |
| rs559412490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010663 | CCGTGCCTGGCCCAT[G/T]ATTCCACCTATTTAA | 55819 |
| rs559418403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950870 | AAATAATGAATCACC[A/G]TTAAATAAGGAGAGA | 55819 |
| rs559425039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011137 | AGGAACACAACACGT[C/T]GGATAAACTCAAATA | 55819 |
| rs559458891 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179988487 | CCTTGAGGTGCATAA[C/G]TGGGCTCTTCATTTG | 55819 |
| rs559470696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002527 | TGTCAGCTCCTTCTC[C/T]GTGGGGTGCATAGCC | 55819 |
| rs559527408 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180068421 | ATATAAAATGTGTTA[G/T]CCCCAGGCAAATGAT | 55819 |
| rs559530765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944913 | ATAAGGCACATATAT[A/T]TGCTCACACGTGGCA | 55819 |
| rs559597522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066905 | TGGCATGCACCTGCA[C/G]TCTCAGCTACTGGGG | 55819 |
| rs559600510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004744 | ATAGGTCACTTTGAT[G/T]AAATTCATCTCAGGT | 55819 |
| rs559614373 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180026075 | AAGAGAATATGATGG[A/G]AAAAAGGTGAAGAGC | 55819 |
| rs559619730 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921793 | TTTGGGAAGGCGAGG[G/T]GGGTGGATCACGAGA | 55819 |
| rs559625075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924704 | TAAGGCAGGAGAATT[A/G]CTTAAACCTGGGAGG | 55819 |
| rs559625448 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180041403 | AATTACATGGCCACT[A/G]TTCTGGATTTTTTGG | 55819 |
| rs559631111 | in-del | -/AAAAAAAAAACAAAAAAAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055271 | AAAAAAAAAAAAAAA[-/AAAAAAAAAACAAAAAAAAA]CAGCAAACAAACAAA | 55819 |
| rs559649343 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180067964 | TTAAACATGAAAACC[G/T]AAGATTCACTTTTTT | 55819 |
| rs559667858 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179938114 | GGTACGCGGCACCAC[A/G]TCTGGCTAATTTTTG | 55819 |
| rs559670255 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179962219 | GGCTGGGGAATGCCA[C/T]CCGACCCTGACATCT | 55819 |
| rs559677489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965077 | AGACTACCTTGTAGA[A/G]CTTCGTCACATCTAT | 55819 |
| rs559702855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179938916 | TCTTGTCCTACCACT[A/G]AAGAGTCAAGGATCA | 55819 |
| rs559718367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978145 | ATGCCCACCCTGAAA[A/G]GGAGGCATACAAAGC | 55819 |
| rs559724858 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180018431 | CAGCAGGAGAGAGAA[C/T]GAGTGCAAGTTGGGG | 55819 |
| rs559746651 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950528 | ACCTTCATGGTTACT[A/G]AGACCATGATTAAAT | 55819 |
| rs559793350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923914 | GAACTTGATGGGCAC[A/G]GAGGTTTGCGCATAT | 55819 |
| rs559802295 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057315 | GCACTTTGGGAGGCC[A/G]AGGCGGGAGGATCAC | 55819 |
| rs559813246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180026844 | CCACTGCAGAGAACC[A/G]AAAGACATGACACAA | 55819 |
| rs559820172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043141 | TGGGCACATAGTAAG[A/T]CCCTCATCTCTACAC | 55819 |
| rs559823575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060917 | TACTAAAAATACAAA[A/T]AATTAGCTGGGCGAG | 55819 |
| rs559836636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997618 | CAGGTGTGAGCCACC[A/G]CGAGTGGCCTTATGT | 55819 |
| rs559863626 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180025852 | TATTACTCATTTTCT[A/T]GATAGGCATTTAGAA | 55819 |
| rs559868840 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001766 | AGCTGTTGTGTGGAC[C/T]CAGCATGGGAGGGGA | 55819 |
| rs559878331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007478 | TTTCCTTTGCTAATA[C/T]TATGGCTTCTCTTTT | 55819 |
| rs559879999 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957678 | AGTCACTCAATCCCT[C/T]GAAGCCCTACTTTAT | 55819 |
| rs559880981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930955 | GCTGAGGCATGAGAA[C/T]CCAGGAGGCAGAGGT | 55819 |
| rs559895741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057421 | GGGCATGGTGGTGCA[C/T]GCCTGTAATTCCAGC | 55819 |
| rs559909870 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954209 | CAAGAAGTTAAACAT[A/G]GAGTTATAACATAAT | 55819 |
| rs559917608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021837 | CTGCCATCCAATCCC[A/G]AAGTCCATCCAAGCT | 55819 |
| rs559939685 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180022625 | CATCAATGTACACGG[-/A]AGCTCACGTGACTGA | 55819 |
| rs559957176 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042205 | ATGCCAGTAACTTCA[C/G]AGAACTATTACATCT | 55819 |
| rs559989454 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180057307 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCGGG | 55819 |
| rs560022751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179920584 | CAAAAAGTGCGGGCA[A/T]CCTTCAATTCACGCA | 55819 |
| rs560046668 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF130 | GRCh38.p7 | 5:179959622 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 55819 |
| rs560111420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952864 | AAAGGTATCTAGTCT[A/G]TAGTCTTAATAGCTA | 55819 |
| rs560115285 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180060914 | CTCTACTAAAAATAC[-/A]AAAAATTAGCTGGGC | 55819 |
| rs560124338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030482 | GGGTCATTTCCATCA[C/T]CCCCCAGAAAATTCA | 55819 |
| rs560128540 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180072110 | AAAGTCCCTCTCGCG[C/T]GGCTGCCGCCTGAGG | 55819 |
| rs560149525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933934 | CAGACTGTTCTGCCA[C/T]TTTTTCTAGATCTTT | 55819 |
| rs560152520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038465 | GTGCTTGGATTATAG[A/G]ATTACAGGTGTGAGC | 55819 |
| rs560165089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000551 | TGCCTAATGTTCCAT[A/T]AGTTTTGTAGGCGTT | 55819 |
| rs560166284 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180039412 | CAGCTAATTTTTTTA[G/T]TTTTAGTAGAGACAG | 55819 |
| rs560186308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022480 | CAGTGTCTTCACTTA[C/T]GTAAATGTGAACTAC | 55819 |
| rs560204259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948385 | GTTCTGTTTGTTGCT[A/C]TTGGCCTGGTGCATT | 55819 |
| rs560219228 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179942624 | AGAGAACAGAATTCT[-/A]TACAGCAAAGCCATT | 55819 |
| rs560227684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993071 | ATCCTTTTTTATGGC[C/T]GCATAGTATTCCATG | 55819 |
| rs560228237 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025528 | AAATTAAGAGCTTAT[G/T]GAAGTTTTAAAATGG | 55819 |
| rs560228760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927690 | GCCTCCCAGGTTCAA[C/G]CAATTCTCCTGCCTC | 55819 |
| rs560233778 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179936087 | AAAAACTAGCTCTTA[G/T]TATTTCTGTTTGCTG | 55819 |
| rs560269308 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179921101 | CCTTTTCTATAAAAC[C/T]GTTTTTAAGCTTTAC | 55819 |
| rs560270376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179928773 | AGCTGGGACTACAGG[C/T]GCCCACCACCACGCC | 55819 |
| rs560270821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179936794 | ATTAATGGAATAAAA[C/T]TGAGAGTCCAGAAAT | 55819 |
| rs560286799 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974042 | CTGCGGGAGGGGAGG[C/T]CTCTATATTGAAGGT | 55819 |
| rs560296051 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981076 | GAAGGGGTTAGATGG[A/G]AAAGGCGTAGGGTTA | 55819 |
| rs560302631 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047367 | CATGGATATAACTTA[C/T]TATTTTACTGCTTCT | 55819 |
| rs560312770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065041 | CTAGAGAAAAAACAC[A/G]CCTTTTTCAACATTT | 55819 |
| rs560351574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058782 | AGCCAGGCTGGTCTC[A/G]AACTCGTGACCTCAA | 55819 |
| rs560353558 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180066426 | TGTCTTTATCAGCAG[C/G]ATGAAAACAGACTAA | 55819 |
| rs560387101 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179944131 | TGCCTGCCACCATGC[C/T]TAGCTTTTTGTATTT | 55819 |
| rs560429645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961984 | AACCCTGCGATATGG[C/T]CCTAGCATTATCTGT | 55819 |
| rs560436860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001115 | CAGTGGTACAGTCTC[C/T]GTGCAGTTTCAGCTG | 55819 |
| rs560437782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059160 | AAGTACATCACAGTT[C/T]TTGCACCTTTTAGTC | 55819 |
| rs560448983 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993850 | CTTTTAGGGTTTTTA[G/T]GGTTTTAAGTCTAAC | 55819 |
| rs560476119 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064208 | TGTTTAGTTTGTGCA[C/T]AATCTCAAATTCCAC | 55819 |
| rs560481841 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179975055 | GGAGCGCCAGCCAGG[A/C]GGGGAGGCTCTGTCT | 55819 |
| rs560496041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986596 | CTGGTGATCACAATA[G/T]CAACAGGTGGCTATG | 55819 |
| rs560501542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975198 | TAGGGGCGGGGAGGC[A/G]TCCCAAGGCAGAAGG | 55819 |
| rs560513969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045993 | ATGGGACCGAGCCCC[A/G]TGGAGCAGGGGGCAG | 55819 |
| rs560540412 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998636 | CTTAACATGTGGCCA[A/G]TCTTGAAGAATATTC | 55819 |
| rs560604704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987296 | CCTCAGCCTCCTGAA[C/T]ACCTGGGACTATAGG | 55819 |
| rs560640393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946029 | TTCCTTCAGCAAGTC[G/T]CAGTTCCCCTGTGCT | 55819 |
| rs560642496 | in-del | -/AAG | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179973852 | ACAGTGAAACCTGAA[-/AAG]CACAAGCATACTGAG | 55819 |
| rs560650983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946588 | AGACGGAGTCTCGCT[C/G]TGTCGCCCAGGCTGG | 55819 |
| rs560683022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996953 | AGTGCTGGACTTTTC[C/T]TTAATGGGAGACTTT | 55819 |
| rs560705118 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179952799 | AAAAACTATTTCATG[A/G]TAAAAACGTTCAATA | 55819 |
| rs560716060 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977967 | TCTGGGGAGTCTGGA[A/G]GCCGCGTGCCACATC | 55819 |
| rs560749298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952142 | GTTCAAGGCTGCAGC[A/G]AGCTGAGATTGTGCC | 55819 |
| rs560763269 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024204 | CTAATGGATCATGAT[G/T]ACTAAATGTAATGTG | 55819 |
| rs560772610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009475 | AGGATATACGGATGG[C/T]AAACAAGCACATAAA | 55819 |
| rs560784930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069347 | GCTGGACTGAAAAAC[G/T]GCGTATGTGTGAAGA | 55819 |
| rs560832516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016332 | GGATCTGAGGAGCTC[A/T]GGCCCAGTTTCACGC | 55819 |
| rs560871623 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179922660 | AAAAAATTCTAGGCC[A/G]GGCACAGTGGCTCAT | 55819 |
| rs560871824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062312 | TGATCCACCTGCCTC[C/T]GCCTCCCAAAGTGCT | 55819 |
| rs560888759 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021922 | TACACTCAGTCGTCA[C/G]GTCATAGCCATCTCC | 55819 |
| rs560891689 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989967 | GGGACTCCTTTGAGC[C/G]TCTACTATAGTATTA | 55819 |
| rs560893429 | in-del | -/AATA | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179991770 | TTATTATTAAATTGT[-/AATA]TATAATGAAATAATT | 55819 |
| rs560908834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063087 | CACCTCATACTGCAC[A/C]GAGACTTCTGATGTC | 55819 |
| rs560925384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976195 | GAAAAAGATAACTCC[A/G]AATGAAACTGGAAAA | 55819 |
| rs560956408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180027806 | TGGCAGAGAAGAAGC[C/T]AGGAACCCTGCTAGC | 55819 |
| rs560977266 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180068146 | CATAATCACATCATC[A/G]ACACAGGGCTTTCTC | 55819 |
| rs560990548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179971527 | GCAGCCCGCCACCAC[A/G]CCCAGCCAATTTTTT | 55819 |
| rs560991544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982328 | TGGTCCAGTTTTTGG[C/G]TGTACTGAAAAGCTG | 55819 |
| rs561023402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179931822 | GACTTTGTAACTGTG[A/G]TTCAGGCCCCCCAGC | 55819 |
| rs561053250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983043 | CTGTTCATGTGTTTT[C/G]CCTATATTTCTGAGT | 55819 |
| rs561056100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027110 | ACTGCTTCTGCCCTA[G/T]GATGAAGGGAGGGCA | 55819 |
| rs561062783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925567 | GCTCTCACTCTGTTG[A/C]CCAAGCTGGAGTGTG | 55819 |
| rs561098191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991380 | TTGTATCTGAATGAC[C/T]AGATGTCTTGCTAAA | 55819 |
| rs561158842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020413 | TGCTGTACGCCACCA[C/T]CACAGGATCCCTCAG | 55819 |
| rs561168777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012380 | CTAACACCTGGAACC[C/T]GGCACCTAGGGTGTG | 55819 |
| rs561173332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057601 | CCTAAAAACTTTAAA[C/G]AACAGGGTTCAGGTA | 55819 |
| rs561189168 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048468 | TAACAAAATCAATGA[C/T]TTAGATTGATTAAAA | 55819 |
| rs561210515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050891 | GAGCTCACTGCTCAA[C/T]TTCCTGGGCTCAAGT | 55819 |
| rs561230462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013331 | AATATAAAATAAATA[C/T]ATAACTCAAGTGACA | 55819 |
| rs561230509 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179953238 | TGAGTTGGAAGACAA[C/T]ATTGTTGAGACAGCA | 55819 |
| rs561241450 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054440 | AATGCACATTCCTTT[C/T]GCATCCTCCCTCTCC | 55819 |
| rs561245061 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043285 | AACTATGATCATGTC[A/G]CTGCACTCCAGCCTG | 55819 |
| rs561263428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998735 | ATTTGGTCTAAAGTG[A/C]AGTTTAAACCCAATG | 55819 |
| rs561277956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923756 | ATTTCGGTCCTGGGG[A/G]CTGCCCAATTCTTCA | 55819 |
| rs561283052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985019 | TTGATATTGTTATCA[C/T]AGCTGCCCCTTGAAC | 55819 |
| rs561302434 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928651 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTAT | 55819 |
| rs561308215 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:179926137 | AATTCCATCCTGTCT[C/T]TGTTCTACCTCTGAT | 55819 |
| rs561312668 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972127 | TTACTCGTAGCCTCT[C/G]TGTGTGGAGTGGTTC | 55819 |
| rs561364351 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948895 | GGCACTTGCTTTCCC[A/G]TGGAGGGTCTTCAGG | 55819 |
| rs561396474 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179963256 | TCTGGATCTTTTCTC[A/C]AACGGGCTGCTCTTG | 55819 |
| rs561437481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029576 | TTTTTACTAATCTTA[A/G]AAATAAAAGCAATAT | 55819 |
| rs561443443 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180043967 | TACTCATTCTACCTA[A/G]TTATTCCCTCCTGTA | 55819 |
| rs561482807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179999492 | TTTGGGAAACCAAGA[C/T]GGGCGGATCACCTGA | 55819 |
| rs561490895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951140 | GAGGTGTATGAATAA[C/T]CAGTGCAGCTTTAAA | 55819 |
| rs561491485 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986616 | AGGTGGCTATGAAAT[G/T]ATTACATTAATACAG | 55819 |
| rs561505345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180051621 | TCAACATGGCAGGAA[C/T]GTCCTAACAGTGGAA | 55819 |
| rs561517872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036558 | CCTGAAGTCTAGAAG[G/T]TTTTCAAAGCATAAA | 55819 |
| rs561556992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941180 | CCTTTTTGGTCATTT[A/G]GTCTTATCTCCTGGC | 55819 |
| rs561559317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987519 | GACTTCCAGCACTAT[A/G]TGGAACAGAGGGGGT | 55819 |
| rs561559770 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179954460 | ATGCTAAGTCAAAGA[C/T]GCCAGACACAAAAGG | 55819 |
| rs561571166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179941934 | GTACATTCTGCAAGT[C/T]TCTGTAAAACATAAG | 55819 |
| rs561574275 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180007669 | TAGCATCTGGAGAGA[C/T]GCTTTGGAAGGATCC | 55819 |
| rs561574285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053287 | GGCCAGGCATATCCC[A/G]GTGAACAGCTGCCCG | 55819 |
| rs561614463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001358 | GTGCTCAGAATGACA[A/G]TGGGACCATGTCCTA | 55819 |
| rs561618920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947458 | ACACCCCACAGCCTG[A/C]CCCTGACACTTGGTG | 55819 |
| rs561620099 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179922153 | GCATTCTAGCAGGAG[C/T]GTAGGAGCTTCTCAT | 55819 |
| rs561625106 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012995 | TGTTAGTAAGATGCA[C/T]GGTCACGACAGATGA | 55819 |
| rs561640580 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016198 | TTTTACAGAATCTGG[C/T]GAAAGTTATATAGGA | 55819 |
| rs561661620 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180055659 | ACAGGATTTACAGAC[A/G]AAATGATCCACTTTT | 55819 |
| rs561670499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984263 | CCACAATGGATGTCT[C/T]TTACGTCTTTTCCTT | 55819 |
| rs561694694 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180002396 | GGCAGCTTAGCCTTA[C/G]GGACAAAGGGGAGCC | 55819 |
| rs561703118 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180055067 | ATAAATTTTGGCCAG[C/G]AGTGGTGGCTCACAC | 55819 |
| rs561760418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179957534 | ACCAAATTTGTCTCC[C/T]TCAACCACATTATTT | 55819 |
| rs561781786 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005256 | AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT | 55819 |
| rs561789509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032075 | TTATCTTGTTGATTT[A/G]TAAGAGTTCTTTATA | 55819 |
| rs561790132 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957121 | TTGTTGCCTCTTAAA[G/T]AAATTATAGGCTGGG | 55819 |
| rs561808059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009387 | GAATACATAAAAAGC[C/T]CTCAAAATTCAACAG | 55819 |
| rs561827430 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980809 | GAGGGCAGAGAAACT[C/G]CAAGGCTGGATTTAT | 55819 |
| rs561834611 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179956802 | ACGCACATGAGGGCA[C/T]AGCCCTGAGCTCTGG | 55819 |
| rs561843666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046231 | GCAGGGCCCGCCAAG[C/G]TCACACCCACGCAGA | 55819 |
| rs561870668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180001922 | CTCAGCTCAGTCACC[A/G]CTCTATTTCTCTGGG | 55819 |
| rs561873346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046768 | GCCTCCTAAGACTGA[C/G]TTGGGTGCTTTTTTC | 55819 |
| rs561952471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944221 | TGATCTGCCTGCCTT[A/G]GCCTCCCAAAGTGTT | 55819 |
| rs561965848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944889 | CATGACAGCAGGCCC[C/T]GTTTCCAGATAAGGC | 55819 |
| rs562022615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180011104 | CACAAAACGCATATA[A/G]CCTGAAACTAATCAC | 55819 |
| rs562035420 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063576 | ATGAACCTAGAGAGG[C/T]CTAGGCTAAAAATCA | 55819 |
| rs562038858 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028179 | TCCTCAACTCCGACT[C/T]GGATGCTGTTTCCTC | 55819 |
| rs562043309 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051736 | TATTTTTTACATCCT[C/T]AGAACGCAAATATAT | 55819 |
| rs562068917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179930345 | ACAGGCATGAGCCAC[C/T]GCACCCGGCCAAAAA | 55819 |
| rs562103267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980983 | GCAGCACAGAGGAGG[C/T]GACTAGGAGGGGTGG | 55819 |
| rs562113380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974706 | TGGAGGGCGATGGCT[C/T]TGAAAGAGAGTTTTA | 55819 |
| rs562114395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179923814 | AAATTTAGTTTCCCT[A/G]AAGTTTTTCTTTTAA | 55819 |
| rs562127997 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969551 | TTCATCCCATACTCA[A/T]CGACCAACAGAAGCA | 55819 |
| rs562141427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025142 | GACCTCTAACACCTA[G/T]AGCCTAAGGCTGCAT | 55819 |
| rs562179855 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029366 | CAGGCAGCATCTCCA[C/T]TGAGAACAGCATGAA | 55819 |
| rs562187331 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067943 | TCGTCTAATAGGATT[A/C]CATTTTTAAACATGA | 55819 |
| rs562210979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179930114 | CCAGGCTAGAGTGCA[A/G]TGGCGTGATCTTGGC | 55819 |
| rs562230629 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056535 | TCTGGCAAAACACAC[G/T]GGGCAGAGGTGGTGT | 55819 |
| rs562239543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021157 | ATTTTTAGTAGAGAC[A/G]GGGATTCACCATGTT | 55819 |
| rs562246735 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023563 | AAAACAAAAATCCAA[C/G]ACCCACAACAATGGA | 55819 |
| rs562257132 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179926367 | TAATAAATCTCAGGC[C/T]GGGTGCGGTGGCTCA | 55819 |
| rs562262039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958946 | TCAGCCTCCCAAAGC[G/T]CTGGGATTATAGGTG | 55819 |
| rs562304282 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180060861 | GATCACGAGGTCGGG[A/C]GATCGAGACCATCCT | 55819 |
| rs562319126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964988 | TAAAAATCAAGAGCC[A/G]AATGTCATCATCATC | 55819 |
| rs562356269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055871 | GGTGGATCATCTGAG[A/G]TCAGGAGTTCAAGAC | 55819 |
| rs562418431 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179932890 | AATTAACCTGTAATT[G/T]TCTTTCTTGTAATGC | 55819 |
| rs562421845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951476 | GCAAACTCCGCCTCC[C/T]GGGTTCACGCCATTC | 55819 |
| rs562431840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179920469 | TAATAGGTCACCAGG[C/T]TTGTGTTTCTCACAT | 55819 |
| rs562437339 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981235 | AGAAAGCTTTGTGCA[C/T]CAGAGGGCCCTAGGA | 55819 |
| rs562444192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996436 | GCTTTTCCACGTTCA[A/G]TATGATGTTGGTTGT | 55819 |
| rs562447450 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005034 | ACCTTATTTTATTAA[C/T]ATCATCTTCCTTTGC | 55819 |
| rs562468206 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179921026 | TATTTTGATTTTAAA[A/T]TTCCATAGTTACATT | 55819 |
| rs562502558 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962811 | ACATTCCCAGTCCTG[A/G]GCGTGCCCTACAGCA | 55819 |
| rs562510315 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180003474 | GGACAAAATATCTCT[A/T]CTCTGTGTTAGGTAT | 55819 |
| rs562523911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044735 | TACTCAGAAGGCTGA[C/G]GCAGGAGAATTGCTT | 55819 |
| rs562538709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179972428 | CCTACACAGGGTGGA[C/T]GATGGGACTTGGCTG | 55819 |
| rs562559810 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028902 | ATGAAAGAAAAATTG[A/T]TTTCATAATTTTATA | 55819 |
| rs562569112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941867 | GTTTCCTTAATGAGG[C/T]TTAATAGAATACTGA | 55819 |
| rs562569906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977666 | AAGACCAACTGGCCA[A/G]CATGATGAAACCCCG | 55819 |
| rs562569908 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | RNF130 | GRCh38.p7 | 5:180012632 | TTTTCATTGATTTCA[-/T]TTTCTGAATAGATAA | 55819 |
| rs562585107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045180 | TCTCATTTGCAATGA[A/G]AGAAGGAGAAGAATA | 55819 |
| rs562587615 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058151 | GTTACTGCTGGGGAG[C/G/T]GAGGAGGGAAGGAGC | 55819 |
| rs562591909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180071160 | GCACCACCTCCTTTG[C/T]CTACGCTGTCCCTGC | 55819 |
| rs562593503 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179961353 | GAGCAACTGTGAAAT[A/C]AACCCTCTACAACTG | 55819 |
| rs562616575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933855 | GTTTTTGTCTTGCTT[C/T]TTCATGGTCCATGTT | 55819 |
| rs562618699 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051440 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGGT | 55819 |
| rs562629560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948334 | TCATGGCAGACCTGG[A/G]ATGGTGGTCTCTGTT | 55819 |
| rs562643479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942793 | CTGTAATGTTTCTTA[A/G]AACATCCTCTGCGAA | 55819 |
| rs562652911 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966682 | GTTTTAACAGCAACA[C/T]ACATCACTTTCTTGG | 55819 |
| rs562653055 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179973227 | AATTCCCATGGCACA[A/T]CCCTCGCTTCCACAA | 55819 |
| rs562653363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926832 | TTGTGGGACTGAGCC[C/T]TCACCCTGGGGGACC | 55819 |
| rs562705101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943269 | CTGGTTTTATGACTG[G/T]GTGGGAGGGATTTTG | 55819 |
| rs562717828 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056475 | AGGACCCAGTAATTA[C/T]TTAGATATGGGAGTG | 55819 |
| rs562726444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179967796 | ACCTGGAACTAATGG[C/T]TTCCTGGGCAAAAGA | 55819 |
| rs562749429 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960829 | ACCCAGAAAATTAAG[C/T]CAGGGCAATTAAGGT | 55819 |
| rs562754673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984137 | TCTTGTATCATGGAA[C/T]CTTGTTAAATCTACT | 55819 |
| rs562779543 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072702 | CCGGGTTCACGTTGC[C/T]ATGAGAGTCTAATGC | 55819 |
| rs562783222 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180058703 | TGAGACTACAGGTGC[A/C]CACCACCACGCCTGG | 55819 |
| rs562796142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180037452 | TCTATCCTCCAACCC[A/G]CACTCAGGAGGCAGC | 55819 |
| rs562824583 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975482 | CTGCTCTAGCTTAAA[C/G]ACTGTCACAAGTACC | 55819 |
| rs562842236 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029203 | AAAATGATTGAGAAT[C/G]TCATAAAAAATTAAA | 55819 |
| rs562866573 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073014 | AGCTAAAAGGAAGAA[G/T]GGGGCAGTGCAGCCG | 55819 |
| rs562903149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179934936 | GATTTAGTTTGTTGT[C/T]CTTTGAGACAAATGC | 55819 |
| rs562912924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180047278 | ATTCATCATTTCTGT[C/T]ATCAATTTCTTAATT | 55819 |
| rs562912987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055813 | CATTACAACTGGTGC[A/G]TGGCTCATGGCTGTA | 55819 |
| rs562948777 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977590 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGG | 55819 |
| rs562949802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047927 | CCTTCAATACTGACG[C/T]TCCCGAGTACTCTGC | 55819 |
| rs562968858 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049050 | TCTGTTTTAAATAAG[A/C]AGAGGCTGGTAGGCA | 55819 |
| rs563017189 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RNF130 | GRCh38.p7 | 5:180038401 | GGGGGAAAAAAAAAA[A/G]GCCTGTTTTGTTTTT | 55819 |
| rs563063600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986548 | TACTCATAAGCGTAT[A/G]TCACATGACATTTCA | 55819 |
| rs563067426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945441 | AGTTCATCTTTTCAT[A/T]CAAGGAAAGAGAAAA | 55819 |
| rs563099847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979227 | AATGCAAGCCGTTTT[G/T]ATGCTGCTTCTATTT | 55819 |
| rs563109491 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003774 | AAATTCTTCCATGAA[A/G]ATCACTTTTTATTAA | 55819 |
| rs563111236 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930278 | GGTCAGGCTGATCTC[A/G]AACTCCTGACCTCGT | 55819 |
| rs563126661 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031370 | CACGCACCTGTAATC[A/C]CAGCTACTCGGGAAG | 55819 |
| rs563145886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975059 | CGCCAGCCAGGCGGG[G/T]AGGCTCTGTCTTGCC | 55819 |
| rs563161193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973995 | TTTCCTATGTCCCAC[A/G]CATGCCATGAACTAG | 55819 |
| rs563176669 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063923 | CAAAAAAGAAGAGAA[A/G]TGAGAAGCCAGGAGG | 55819 |
| rs563178695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945994 | GCCCAGCTGTGAGTG[A/C]CAGAAGCATATGACT | 55819 |
| rs563183915 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937706 | CTGCTAGGTATATAA[A/C/T]CCAAAGAATTGAAAA | 55819 |
| rs563185120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024057 | CCCATATCCCTAGCC[C/T]AATTATAAGAAAACT | 55819 |
| rs563185232 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015475 | AGGAGTAGGGAAAGG[A/T]GTAGGGAAAGGAGTA | 55819 |
| rs563210354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928691 | TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG | 55819 |
| rs563210712 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179975431 | CCCACACAATGACCT[C/G]GTCCCAAATGTCAAC | 55819 |
| rs563233972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995628 | GGTTGTTCCTTCTCA[A/G]TGTCTCTCAGCTACT | 55819 |
| rs563278644 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042907 | GGTCTAGATCAACTG[C/G]TTACTAGCTGTGTAA | 55819 |
| rs563279581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957841 | AAGACGGGCTGTGTG[A/G]GCAAAAGGTTATCAG | 55819 |
| rs563321564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970879 | GAGTTTCAAAAAGAT[A/G]CTAAATCATGGCTAA | 55819 |
| rs563332726 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179989930 | TTATGATGGCAAATA[A/T]CAACCTTTTGTTTCC | 55819 |
| rs563342777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982166 | GTACTACTGTGTGTA[C/T]GGCTTCTTTGACTCA | 55819 |
| rs563353384 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041529 | ATCCTCTGCAAATCT[A/T]AAGAAGAAGCCCCCG | 55819 |
| rs563371364 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180034236 | ATCCCATTCCTGGGG[C/T]AATGAATCTAATCCA | 55819 |
| rs563378207 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179966556 | GGTTTATAAAACAGC[C/G]ACTAAGACAGACCTC | 55819 |
| rs563416608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033682 | GCCTGGGCAACAGAG[C/T]GAGACTCTGCCTTTA | 55819 |
| rs563490203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179981485 | CAGAGAATGATTTAA[C/T]AAAGCCTTCCCTATG | 55819 |
| rs563498642 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045455 | TAAAGACCGCAGGGA[A/C]CCAAACAGTGAGCAG | 55819 |
| rs563501139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997860 | TTTTCACTTGTTTTT[G/T]GAGACAGAGTCTTGC | 55819 |
| rs563507569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026240 | TCTTCCTTTCAACAA[C/T]GGAAAGAATGTCCAC | 55819 |
| rs563537057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939060 | ATGGTGAGACCCCAT[C/T]TCTACTAAAAATACA | 55819 |
| rs563562256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179990681 | CGCTTGGTAATGGGC[A/G]TCTTCCCAGACACTG | 55819 |
| rs563575883 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179930351 | ATGAGCCACTGCACC[C/T]GGCCAAAAATTTCAT | 55819 |
| rs563578205 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062216 | CGCACAGCCACGCCT[A/C]GATAATTTTTGTTAT | 55819 |
| rs563581545 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | RNF130 | GRCh38.p7 | 5:180019363 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 55819 |
| rs563586316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965711 | TGGTGAGAAATGAGC[C/T]AAACTACACTCAAAG | 55819 |
| rs563646720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959847 | TGCTCTAGTTATTTC[A/G]TCACCTTTACCACTT | 55819 |
| rs563673443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011308 | AAAACCCAAAAAAGG[C/T]CTATCAATCAGATAA | 55819 |
| rs563680019 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180004933 | CACCATTTTTTCCCA[C/T]TTTTTTTTCTCAAAA | 55819 |
| rs563742966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965148 | TTTGTGTGTGTGTGA[C/T]TGCAATTTTAAAAAC | 55819 |
| rs563746149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973946 | GAACATGAAAGGAAC[A/C]AACCCAGCAATCATG | 55819 |
| rs563755183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179959029 | CCTCCCTGTAGATAT[C/T]GCCAGAGCTCCAGAA | 55819 |
| rs563801829 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947420 | TACTATCATGCTCTG[A/C]ACACTAGGGGCCACT | 55819 |
| rs563802896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010179 | GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTAAGC | 55819 |
| rs563878340 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:180050672 | TTCTTTCAATGAGGA[A/T]CTGTTAGGTAAACTT | 55819 |
| rs563879478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065116 | AATTCATTTTGTTCT[G/T]GGAGCTACAGAATGA | 55819 |
| rs563898743 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179952947 | AACACATGGATGTCT[C/G]TTTGCACCATTTCTA | 55819 |
| rs563929120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180043899 | AAAAAGTGGTATTTA[C/T]TATTCAGAAGAAAAT | 55819 |
| rs563933930 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179968033 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs563965077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035072 | CTCTAATCTTTATTA[A/G]CTCCTTTGTTCTACT | 55819 |
| rs563968945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953817 | TACCAAGAAAGTGAA[C/T]AAATAGTTTAGAGAA | 55819 |
| rs563995313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179946800 | ACCTCGTGATCCACC[A/C]GCCTCGGCCTCCCAA | 55819 |
| rs563999243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179962062 | TTACAACTGAAAAAC[A/G]GAGGAGCTGAGAGTC | 55819 |
| rs564019657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179921186 | GAGTTCTGACAGCTG[C/T]ATAGGCCAGTGACAC | 55819 |
| rs564028581 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034204 | TTGATTTTCAGATGT[-/A]AAAAAAAAAACCATA | 55819 |
| rs564065193 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072610 | TTTCCGGATGAGGCT[G/T]CTCCACCTCAGATCA | 55819 |
| rs564069737 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999560 | AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 55819 |
| rs564071821 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179994409 | GTGGTTTGTAGTTCT[C/T]CTTGAAGAGGTCCTT | 55819 |
| rs564113479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058841 | TGCTGGGATTACAGG[C/T]TGAGCCACTGCACCC | 55819 |
| rs564152486 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180065738 | GCATTCTAGCCTGGG[C/T]GACAGAGTGAGACTC | 55819 |
| rs564171693 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180046039 | CTCCAGTGGCGTGGA[C/T]GGAGGGGGGTGGGGC | 55819 |
| rs564172132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031949 | TTATGATCATTCTAG[A/G]GGATGTGAAATAGTA | 55819 |
| rs564178686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968283 | CTGGGCGACAGAGCA[A/C]GACTGTCTCAAAACA | 55819 |
| rs564192776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015441 | TCTTGAAGACTCAAG[C/T]TGGAAAAGGAGTAGG | 55819 |
| rs564216090 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954465 | AAGTCAAAGACGCCA[A/G]ACACAAAAGGCCACA | 55819 |
| rs564218670 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930847 | AGTTCAAGACCAGCC[C/T]AGTAAACATAACAAA | 55819 |
| rs564238176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180032650 | TCAATTGACCGTAAA[A/G]ATATTTATTTCTAGA | 55819 |
| rs564252414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180025014 | CTCTGTAATACAAAA[C/G]ACAGACCTGCAGAGC | 55819 |
| rs564252999 | snp | C/T | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:180008573 | GAATCAAACCAGAAA[C/T]CAGTAACACTAAGAT | 55819 |
| rs564253405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986643 | ACAGTACGTACTACT[A/G]TTAATTTTATGCGGT | 55819 |
| rs564295215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930081 | TTATTTTTTGAGATG[C/G]AGTCTTACTCTTGTC | 55819 |
| rs564365200 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180046207 | AGCCCCTCACTGACC[A/G]GGGCAGGTGCAGGGC | 55819 |
| rs564395094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949862 | CTCCTCAAGGAGCAA[C/T]CTGTAATCAATCGGA | 55819 |
| rs564426528 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180039566 | AGGGCACTAAAGTTG[A/C]AATCCATCTGCACCA | 55819 |
| rs564435337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016429 | ATAATTAGACTGTAA[C/T]GCTGTAAATATCAAA | 55819 |
| rs564439365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937756 | CTGCAAACCAATGTT[C/T]ACAGTATTGTTCATC | 55819 |
| rs564445211 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180066621 | CGGGCAGATCACCTG[A/T]GGTTGGGAGTTCGAG | 55819 |
| rs564466939 | snp | C/T | 6.58946e-05 | 0.0057396 | missense | RNF130 | GRCh38.p7 | 5:179980196 | GCTGCATCTCCGAGA[C/T]GACGCTATGAAAATT | 55819 |
| rs564482369 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947074 | CCCTACTGTACTGAA[C/T]GAATTCTTCACGGAA | 55819 |
| rs564499898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179987442 | CCAAAGTGCTGCGAT[C/T]ACAGGTGTGAGCCAC | 55819 |
| rs564510543 | snp | C/T | 3.29478e-05 | 0.00405867 | missense | RNF130 | GRCh38.p7 | 5:179980170 | TTGTCAATTTACTGA[C/T]GGCTTTCTTGGCTGC | 55819 |
| rs564539912 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179944190 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 55819 |
| rs564582784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937017 | CGATGGAAGTTTTTG[C/T]GACCACCAATTTGTC | 55819 |
| rs564602950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180060845 | GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCGGG | 55819 |
| rs564637138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035613 | GTTAAAATCTCCAAC[C/T]ATAATGATTGAAATG | 55819 |
| rs564638022 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986865 | TTCATCAGTATTTGA[C/G]AATATTGGTTAAATT | 55819 |
| rs564648900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968877 | CGATGCACAGGACAG[A/C]CCCCACAAGAAGGGA | 55819 |
| rs564649743 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180028681 | GGGAGGAAGTGTTCC[C/T]GGCAAACACTCACTC | 55819 |
| rs564655162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067310 | GCCCATCATTGTACA[C/T]ATTAAGATCTTTGCA | 55819 |
| rs564655976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932067 | ATAAATTTGTTTCCT[C/T]TTCTTTGTTTCACTT | 55819 |
| rs564662281 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921754 | GTGAGCCAAGATCGC[A/C/G]CCACACGCCTGTCAT | 55819 |
| rs564666491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974654 | GGAGGGAAGAGGCAG[G/T]GGGCAGGTGTGACAG | 55819 |
| rs564671361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017271 | CAAGGTGATGGCGTG[A/T]CCCTCCTCAGCTCGT | 55819 |
| rs564671800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010372 | CATTTTTTTCTTTAT[C/T]TTTTTGAAACAGAGT | 55819 |
| rs564694711 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179932804 | TTGTACCACTGCACT[C/G]CAGCCTGGGCAACAG | 55819 |
| rs564742972 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180060323 | TAAGCCATGAAAGAT[A/T]CACTTCTTTTCCTTC | 55819 |
| rs564760134 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179946602 | TCTGTCGCCCAGGCT[A/G]GAGTGCAGTGGTGTG | 55819 |
| rs564773681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964016 | CGGAGCAGCAGTTCT[C/T]CAGGTCCTGTGGGTG | 55819 |
| rs564779912 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021805 | CCCCAAATAAGGAGC[A/T]TAACACTGATGTGTC | 55819 |
| rs564783833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010029 | GAGGTGGGCGGATCA[A/C]AAGGTCAGGAGATCG | 55819 |
| rs564792412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180020338 | CGGAGAGGAAGAACG[C/T]GGTCTGCTGCACAAA | 55819 |
| rs564817047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057651 | CCAAGAGGATTATTA[C/T]ACCCCCGCAATACCG | 55819 |
| rs564818177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179923139 | TCACTAAGATTTTCT[C/T]GTACATGTTCATCTA | 55819 |
| rs564824172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940428 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCTTT | 55819 |
| rs564860549 | in-del | -/AAAC | 0.124144 | 0.21601 | intron-variant | RNF130 | GRCh38.p7 | 5:179968293 | AGCAAGACTGTCTCA[-/AAAC]AAACAAACAAACAAA | 55819 |
| rs564861154 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967368 | CTTCATGGTAAATGT[C/T]CATGTTGAAGAATCC | 55819 |
| rs564886072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070453 | GCATACAAATACAGA[C/T]CTCAGAGGGGCATAA | 55819 |
| rs564893813 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179983096 | AGAGAACATTATATA[C/T]TCCAGATAAAAATCC | 55819 |
| rs564987007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179953941 | AATGGGTAAAGCACC[A/G]GGATAGACATTTCTC | 55819 |
| rs564995320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954508 | CTATTTACATGAAAT[A/G]CCCAGAACAGGCAAA | 55819 |
| rs565001587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180020519 | CTGGGAAGCCGAATG[C/T]GTAAGCCACTGAGTG | 55819 |
| rs565006655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976282 | GGCCGAGCCTCCCCT[A/G]AGGGAAGATCCCCTC | 55819 |
| rs565013740 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948663 | ATGATAGATAGAGCG[A/G]GACTCTGTCTCAAAA | 55819 |
| rs565026324 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925455 | TGTCAACCAAAAAGA[A/G]AAATAACAGGCATTG | 55819 |
| rs565042547 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926142 | CATCCTGTCTTTGTT[C/T]TACCTCTGATAAATG | 55819 |
| rs565070276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976994 | GGAGAAACCAACATG[C/T]TGTTTCCAGGGCAAC | 55819 |
| rs565078058 | snp | C/T | 4.95184e-05 | 0.00497562 | intron-variant | RNF130 | GRCh38.p7 | 5:179980252 | AAGATCTCTGAATGA[C/T]GTACTTTATTTTTAA | 55819 |
| rs565141804 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046729 | AGGATTCTGCCAAAA[C/T]GTCTTCTCCAGAACG | 55819 |
| rs565156779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977841 | CCTGGGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 55819 |
| rs565162460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063781 | TGTTGAGCTGTAGGA[A/C]GCATGAGAAAGACCA | 55819 |
| rs565168469 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017043 | GTTTTGTGTCCAGGA[C/T]TCAATCGGGGCTGTC | 55819 |
| rs565194562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180044583 | TCACGCTTGTAATCC[C/T]AGCACTTTGGGAGGC | 55819 |
| rs565225103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005701 | AGCTCCAAGGTCACA[A/G]CCTACCTTCTCTGTG | 55819 |
| rs565237772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998798 | ATGCTAAGAGTGGGG[C/T]GTTGAATTCCCCAAC | 55819 |
| rs565249107 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061280 | CTTTTGGAAAAAACC[A/G]CAACAACTGACGTGA | 55819 |
| rs565256388 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016095 | AAGAGCCGGGCAGAG[C/G]AGCCCGACCCTGCCG | 55819 |
| rs565279753 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179992211 | CAGTGGCACGATCTC[A/G]GCTCACTGTAAACTC | 55819 |
| rs565319140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179956306 | GTTAGCGTTGATCTT[C/T]TTCTTTCTGCTGAGC | 55819 |
| rs565319966 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042166 | AACTAAATGCTTACA[C/T]GACTTAAATTGTAAA | 55819 |
| rs565371975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942144 | TTTGTGTCCAAATAG[A/G]TTTCACTTAGAACCA | 55819 |
| rs565401059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045065 | AAAACACAGAGCAAA[A/G]ACTAAACTCTTCTCT | 55819 |
| rs565419879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987053 | GAGTTTTTGGTGAAC[A/T]CTTTGTTTTTTTTCT | 55819 |
| rs565427864 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060338 | TCACTTCTTTTCCTT[C/T]CGTGCAGTGGCTCCT | 55819 |
| rs565456637 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072198 | GGCGCAGTCCCGCCC[C/T]GAGCGCATGCGTGCC | 55819 |
| rs565494560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986019 | AACTTTTCAAACTAA[C/T]GTTTGCTGCCATTAA | 55819 |
| rs565508946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037375 | AGTTGTGCTCCACCG[C/T]AGGCATCCATGGCCC | 55819 |
| rs565515821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029901 | TTGCCTAGGCTAGAG[C/T]GCAGTGGCACAATCT | 55819 |
| rs565556494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179934035 | TTCCCAGCTCTGTGA[C/T]GATCAGATTTCAGAT | 55819 |
| rs565557964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974512 | AGAGGAAAAGGAAAC[A/G]TCACGTGGCAAGAAG | 55819 |
| rs565564337 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992917 | TGTGATGTTCCCCAT[-/C]CCTGTGTCCAAGTGT | 55819 |
| rs565589098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180022624 | CACATCAATGTACAC[A/G]GAGCTCACGTGACTG | 55819 |
| rs565617930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179994669 | TATCGGGTGGGTGAG[C/T]TGGCTCATAACCTCC | 55819 |
| rs565638123 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994054 | TGTGTGGTATTATTT[C/T]TGAGGGCTCTGTTCT | 55819 |
| rs565639988 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179985305 | TTCATGGCATTTCCT[-/ATA]ATAATAATGACATCT | 55819 |
| rs565656514 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180046115 | ACGAGAATCTGTGCG[C/T]GGTGGACCGCGGCGC | 55819 |
| rs565670302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974750 | GAAATGCGAGTGTCA[C/T]GAGATGCCGGCGAGT | 55819 |
| rs565708903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010108 | AAAAATTAGCCAGGC[A/G]CGGTGGCAGGCACCT | 55819 |
| rs565742563 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180039888 | CATACATCATGCATG[G/T]TTATTGTAAAGACTG | 55819 |
| rs565785930 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014923 | TCCAGGAAGTTGAGG[C/T]TGCAGTGAGCTGAGA | 55819 |
| rs565845283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180017661 | GGGTGGGCAGTTTTT[C/T]GGAAAAGAGCCCCCC | 55819 |
| rs565854551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067445 | AAATCAGAGGCAGTA[A/G]ATGTAGATAACGTTT | 55819 |
| rs565855832 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073403 | AATAAAAAAATTAGT[C/T]GTGGTGATGCGTGCC | 55819 |
| rs565899065 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941556 | TGCTTGAGCTCTCCT[C/T]CTCTCTCGGTCTTTG | 55819 |
| rs565903598 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024572 | TGTCAACACAAAAAT[G/T]TATACCTGTCTTTGA | 55819 |
| rs565924851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179937287 | GAATGGAGAAAACAT[C/T]TGTAAATCACGTATC | 55819 |
| rs565961383 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016630 | TTTTCTTGAGAAACT[G/T]CCCCCACTGTTATTC | 55819 |
| rs565961843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179929789 | GGTCCAGTTTCAATA[C/T]ACACACCCACACCCA | 55819 |
| rs565978473 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012095 | TTTCAGATGAGAAAG[A/C]AGCTGAGATGCTCAA | 55819 |
| rs565996686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179969005 | CCCAACTGTATACAC[C/T]GAAACTGTGTTTGAC | 55819 |
| rs565998353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060102 | CACAGGCAGCTTCTA[C/T]AAGCTGAAAAAGGCA | 55819 |
| rs565998358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930192 | CCTCCCGAGTAGCTG[A/G]GATTACAGGCATCTG | 55819 |
| rs566026148 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179933668 | CTGAGACCACAGTCA[C/T]GCTCCACCATGCCGG | 55819 |
| rs566034120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060565 | TTACCAACACACCGC[A/G]AGGGCCTGTCCGTTC | 55819 |
| rs566055365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034440 | TGTGAAGGATTAGTA[C/T]TATTTTTTCTTTAAA | 55819 |
| rs566057519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026523 | GAAACCACACAATGA[C/G]TAGCCTTTCCTGTCA | 55819 |
| rs566079144 | snp | A/G | 0.000177592 | 0.00942148 | intron-variant, synonymous-codon | RNF130 | GRCh38.p7 | 5:179963548 | GAGGCCAAAACTGGC[A/G]ATAATAAACCATTCT | 55819 |
| rs566090607 | in-del | -/GAGGCAGGA | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180044732 | GCTACTCAGAAGGCT[-/GAGGCAGGA]GAGGCAGGAGAATTG | 55819 |
| rs566092442 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179992703 | TTTTAGTTGAAGTGG[G/T]ATTATTTTTTATTTT | 55819 |
| rs566108238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996502 | ATGTTCTTTCTATAC[C/T]TAACTTGTTAAGAGT | 55819 |
| rs566152750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957971 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 55819 |
| rs566155368 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179969727 | AGGCACGGTGGCTCA[C/T]GCCTGTAACCCCAGC | 55819 |
| rs566156530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056045 | GCTGAGATGGTGTCA[C/T]CGTACTCTGGCCTGG | 55819 |
| rs566161217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180013577 | TTAACTTGTCTGACA[A/G]CTACATTTTTAAAAA | 55819 |
| rs566234993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006855 | ACTTAATTTGACAGC[A/G]ACATTTAAGTTTACC | 55819 |
| rs566249553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041052 | GCCTCTCCACACACC[A/G]CCACCACCGCTATCC | 55819 |
| rs566260371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958486 | CCAACAGCTCTCCTC[A/G]GCCTCTGATCCCTCC | 55819 |
| rs566317166 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044325 | AGATAGATAATACAA[A/C]ATATTTTACTACAGA | 55819 |
| rs566322080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179951532 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 55819 |
| rs566377939 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954504 | GGTTCTATTTACATG[A/C]AATGCCCAGAACAGG | 55819 |
| rs566390473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037074 | TAACTTACTGTGTTT[C/G]GGAGACTTATTCATG | 55819 |
| rs566416887 | in-del | -/A | 0.00835141 | 0.0640778 | intron-variant | RNF130 | GRCh38.p7 | 5:179921866 | CTCTACTAAAAATAC[-/A]AAAAAATTAGCCAGG | 55819 |
| rs566420019 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039359 | ATTTTCCTGTCTCAG[C/T]CTCAGTAGCTGGGAT | 55819 |
| rs566421439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051318 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAAGCT | 55819 |
| rs566421825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981635 | TTTTCACTAAGCACC[C/T]CTAATAGACACGGGC | 55819 |
| rs566422425 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179926433 | GGCGGATCACCTGAG[A/G]TCAGGAGTTTGAGAC | 55819 |
| rs566428242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180063385 | AGCAAGGATGGTCCT[A/G]ATTTGTGTAAATAAC | 55819 |
| rs566448006 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179999126 | CTTGCAGGTTCAAGC[A/G]ATTCTCTGCCTCAGA | 55819 |
| rs566449417 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179942372 | ACTGAGGCAGACAGA[C/T]CTGTATGCACTGATG | 55819 |
| rs566459494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972525 | GGCATCCCGCTGGGG[G/T]TCGGGGGAGGCCTAG | 55819 |
| rs566474386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966183 | AGCATTTCTTTCCTG[C/T]TAGTCGACAGTGCAA | 55819 |
| rs566516728 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072981 | GCGTTTAAAAGATAC[A/C]CATCGCTATAAAGTA | 55819 |
| rs566548914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058283 | CAGGCTGCAGACTTA[C/T]GGTTGTGTATTTTTC | 55819 |
| rs566556429 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919895 | AGCACCTGTACTCCA[C/T]GCGGGTAGGAAGCTT | 55819 |
| rs566566935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030818 | GTGTCTGGCTTCTTT[A/C]GTTTAGCATAATGCT | 55819 |
| rs566607992 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179935023 | GCTTTAGCTGAATTA[C/T]GTAAGTTTTGATATG | 55819 |
| rs566623615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180051929 | CTGAAAATTAGAGCT[C/T]GGTCCTCATACAAAG | 55819 |
| rs566627722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999877 | TGGTAGGTGAGGACT[C/T]ATTCCTATCAATTTT | 55819 |
| rs566676816 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180058957 | ATGACTTAACAGTTA[C/G]ATGGTCAATTTATAC | 55819 |
| rs566704473 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954661 | ACAACTGTGTGACTA[C/T]ACTAAGAACTACTGA | 55819 |
| rs566717167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947788 | TATATAGTAGGTATA[C/T]ATTGATATAGCATAT | 55819 |
| rs566757742 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179924186 | CCTGTCCCTAAACAA[-/TT]TTTTTTTTTTAATAA | 55819 |
| rs566764362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059363 | CTATGATTAAATAAT[C/G]GTGTTATGACCTGTG | 55819 |
| rs566792978 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179955724 | GTAGTCAAATGTTTA[A/C]AATAACAGAGAAGTG | 55819 |
| rs566832436 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986171 | AGGCTGCAAAAGGTA[A/T]TTAGCAAAAAGTATA | 55819 |
| rs566835293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927300 | CCTGGAAATACACCA[C/G]ATGTGTACTGGTCAA | 55819 |
| rs566875028 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947278 | ACCTTCCAAAATGCA[A/T]GGGCCTCCTGACTGC | 55819 |
| rs566900377 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041637 | GTCACCAAAGGTAGA[C/G]TCTGCAGACTGCTGG | 55819 |
| rs566956568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945672 | TGTGTGTTGAATGTA[C/T]CGGAGGTGCAGGTGA | 55819 |
| rs566963612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968331 | AAAAAGAAGGCGGCG[A/G]CTAGCGGTAACAACA | 55819 |
| rs566968461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179938240 | TGGGATCACAGGCAC[A/G]AGTCACCGCGCCCAA | 55819 |
| rs566975516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928074 | CTGGCCACCACACAA[C/T]TGATTGGTCTAATCT | 55819 |
| rs566983357 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015776 | AAAGGAGTAGGGAAA[A/G]GAAAGCTGAACAGGT | 55819 |
| rs566990885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179973676 | TCTCATTATGGAAGG[C/T]GCTCCATGGACACCC | 55819 |
| rs566991962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052943 | GTGACACTTGTTGAG[A/G]CAGGTCTCAAGATTG | 55819 |
| rs567006069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179939173 | AGTGAGCTGAGGTCG[C/T]GCCACTGCACTCCAG | 55819 |
| rs567032625 | in-del | -/GAGT | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179929731 | CCAGCCTGGGTGACA[-/GAGT]GAGACTGTGTCTCAA | 55819 |
| rs567054151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968122 | AACACGGTGAAACCC[C/T]GTCTCTACTAACAAT | 55819 |
| rs567091445 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951846 | AAAGAAGAAATAACA[A/G]GGGGAAACCAGATAT | 55819 |
| rs567099168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007889 | ACACCCAGTCCACTA[A/G]CACAGGCTTGCCTGT | 55819 |
| rs567131190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053427 | TGATGAGAAAGAAAA[C/T]GACACATTTTATGAA | 55819 |
| rs567132873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964731 | AGCACTGCTCCTGGG[A/G]ACTTCCGGTCCAGAG | 55819 |
| rs567146282 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924435 | AGGAGGCGGAGGTTG[A/C]GGTGAGCTGAGATTG | 55819 |
| rs567161648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008740 | AAAATACAAGTTAGC[C/T]GGACACGGTGGCATG | 55819 |
| rs567177678 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001401 | CACAAATGTATTTGT[C/G]GCACCTGTGGCAAAG | 55819 |
| rs567189310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965203 | ATCATAAAACACCCA[A/G]TATGCTGGCAGCATT | 55819 |
| rs567193800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958714 | TTTTTGAGACAGAGT[C/T]TCACTCTGGTCACCC | 55819 |
| rs567198953 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179999620 | TATTCAGGAGGCTGA[-/G]GCAGGAGAGTTGTTT | 55819 |
| rs567206486 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923566 | TCAGCCAATCCCAGC[A/C/G]GCTGAGTTTCAGCCA | 55819 |
| rs567220936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989389 | TGGAGTGTATCTATC[C/T]CTTGAGGCCTAGTAA | 55819 |
| rs567231387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180033174 | TTTTGTAGAGACAGG[A/G]TCCCCCTATGTTGCC | 55819 |
| rs567245582 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180074030 | AAACTGTAAGGTGCC[C/T]ATGACCCCTGGCACA | 55819 |
| rs567270690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930463 | AATATATTGAATTTT[A/C]TACATGTAATCGTTT | 55819 |
| rs567285103 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179975151 | TACAGAAAGCCACAG[A/C]AGGTAACACCGACTC | 55819 |
| rs567287170 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965113 | CAAATTCTGAGTCTA[C/T]CATCCCGTATTTGCA | 55819 |
| rs567306825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924145 | AGCCCGGGAGTTCAA[A/G]TCCAGCCTGGGCAAC | 55819 |
| rs567330060 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987821 | CGGGACAAATCCCAC[A/G]TTATATTGCTGTATT | 55819 |
| rs567338385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179930211 | TACAGGCATCTGCCA[C/T]CACACCCGGCTAATT | 55819 |
| rs567346029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970338 | CCTCCTATTATGCCA[A/T]TTATGTTATATTGTA | 55819 |
| rs567354043 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950118 | TGCTTATTAAATAAC[-/T]TTTTTTTTTCTTGAG | 55819 |
| rs567367408 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045867 | GTGCATTTACAATCC[G/T]TTAGCTAGACAGAAA | 55819 |
| rs567450004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004254 | TTCAAAGCATTTTCC[C/T]GTAATACGCTACCCA | 55819 |
| rs567456723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179970956 | AATGTCATTTAAAAC[A/T]TCATTTTTAAAAACT | 55819 |
| rs567481674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179983247 | TTACAAAGACTTCCC[C/T]GTTTTCTCTTCTAGA | 55819 |
| rs567492804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056125 | AAACAAACAAACCAT[A/C]ACCACCAATCAGATT | 55819 |
| rs567513741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180049251 | CTCCTTCCCTCACTC[A/G]AGGGAAACATGAGCT | 55819 |
| rs567517509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997376 | TCACCCAGGCTGGAG[C/T]GCACTGGCGCAATCT | 55819 |
| rs567555685 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180011379 | ACTATGGTTATGTAA[C/G]AGAATGTTCTTGTTT | 55819 |
| rs567599225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056840 | ATAAAGCAGATCACC[A/G]ACAAAACCACTGCTA | 55819 |
| rs567664447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042524 | AAACTTTAAAATCCT[A/G]AAACAGATTGTTTAC | 55819 |
| rs567700733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180050062 | CAACAGAAATGTATT[C/T]TCCCACAGTTCTGAA | 55819 |
| rs567701267 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066563 | CCTGGGCAATACAGC[A/G]AGACCCTGTCTCTAT | 55819 |
| rs567727403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998070 | TGGTCTTGATCTCTT[C/G]ACCTCGTGATCCGCC | 55819 |
| rs567754458 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179968111 | CCATCCTGGCTAACA[A/C]GGTGAAACCCCGTCT | 55819 |
| rs567754794 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991498 | TCAGTTTAGTTGCTT[-/TA]TATAGTCCATGCTTC | 55819 |
| rs567767546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940103 | TTAATATCCTCAGAC[A/C]AGGCATGTCTGCACA | 55819 |
| rs567775552 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001709 | TCTTAGATCTGTGAA[G/T]TCCAGTGCAATGACA | 55819 |
| rs567785757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179976416 | CCTTGGCTTCTCCTG[C/G]TCATTCCAGTGTTGA | 55819 |
| rs567791133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179993213 | TCTTTATAGCAGCAC[A/G]ATTTATAGTCCTTTG | 55819 |
| rs567833502 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180065208 | TACAACTTTTCCCCC[-/T]GTCCTTTCATGGAAA | 55819 |
| rs567864508 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179994012 | TCTTGTTTTTGTCAG[A/C]TTTGTCAAAGATCCG | 55819 |
| rs567864724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986967 | CAGTTTGTTACTGGT[A/G]TACAGAAATGATACT | 55819 |
| rs567883051 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179925851 | TTTATTCTGAGCCAA[A/G]TTGGAAGACGTAGGC | 55819 |
| rs567885830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070062 | CAGCTCTTGCTCCAC[A/G]ACAGCTTGCCTCCCC | 55819 |
| rs567889660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922010 | TGTGTGACAGAGTGA[A/G]ACTCCGTCTGAAAAA | 55819 |
| rs567927731 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:179946836 | TGGGATTACAGACGT[C/G]AGCCACCGCGCCCAG | 55819 |
| rs567943461 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954808 | GAATACGTTCTCACT[C/T]CTCAGGTAAGCTGAG | 55819 |
| rs567962564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021279 | AGGCGTGAGCCACTG[C/T]GCCTGGCCAAAATCT | 55819 |
| rs567973299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062857 | ATTCTCAATCTGTCC[C/T]GTTAACTGGCCATTT | 55819 |
| rs568007819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180052858 | TTCTTAATCTGAGAC[A/G]TCCATAAACCAATAA | 55819 |
| rs568011824 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180000715 | TTCATTCATTGAATT[A/C]TTCAGCTGCAGGATT | 55819 |
| rs568011891 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932294 | AGGGAGTCTCGCCCT[C/G]TTGCCTAGGCTGGAG | 55819 |
| rs568027542 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016052 | GAAGAGAAGCCGCTC[A/G]CGGTGGCGTCATTAC | 55819 |
| rs568030029 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962184 | TTCACCTGCTGGATG[A/T]GGTGCAGTGCTCCTC | 55819 |
| rs568064554 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958026 | GGGACTACAGGCGCC[C/T]GCCACTACGCCCGGC | 55819 |
| rs568066272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180045548 | CACGTTGCCGCTGCT[A/G]GCTCGGGCAGCCTGC | 55819 |
| rs568075383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922289 | TTTAGTCCATTAAAA[A/C]AACTGGGCTTTTAAA | 55819 |
| rs568085377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003594 | TCCTTTAACATTTCC[C/T]ATCACTTTGCGACAG | 55819 |
| rs568090268 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955422 | GCAATCTGGGTCTGC[A/G]AGCTTCAAATCAGCC | 55819 |
| rs568124143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978691 | TCACTTAAACACACA[C/T]CTAAGTACAGACAGG | 55819 |
| rs568127902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046098 | GAGGCATCTGAGGCC[C/G]CACGAGAATCTGTGC | 55819 |
| rs568149704 | snp | C/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955550 | TGAAAAAATAAAATG[C/T]ACTAAAAATAAATGC | 55819 |
| rs568151883 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981786 | TGTTTGAATCAAGAT[A/G]CAAAATCCACACACT | 55819 |
| rs568168663 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:180030574 | ATGGGGGTTTTGCTG[G/T]GTTGCCCAGGCTTAG | 55819 |
| rs568176485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179942993 | TGAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA | 55819 |
| rs568201095 | snp | C/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072547 | TTGGCACTGGGGGAC[C/G]GGTTTCCAGGAAGAG | 55819 |
| rs568241015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180038607 | ACTGTTTCCCCATGA[A/G]TCCTCTAGGAACATA | 55819 |
| rs568244828 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934846 | ATGAGCTACCATGCT[C/T]GGCTTGGTTGATTTT | 55819 |
| rs568260399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979595 | TAGCGGAGAAGCAGG[A/G]CTCTACCATAACTAG | 55819 |
| rs568300921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023828 | ATAAATCCCCACTTA[C/T]TAAGTGTGGGCTGTG | 55819 |
| rs568323709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929473 | TAGGATCAGGCTGGG[C/T]GTGGTGGCTCACACC | 55819 |
| rs568329611 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179936276 | AGGTAATTAAAAAAA[A/T]TTTTTTGTAGAGACA | 55819 |
| rs568367676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179928889 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 55819 |
| rs568370161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974160 | CAAGAACTCTCTTCT[A/G]CTAGCTGGGGCTGGC | 55819 |
| rs568373664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066168 | ACATGCTGTGGGAGG[A/G]ACCCAGTGGGAGATA | 55819 |
| rs568388461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008898 | CAAAAGGAAAAAAAA[A/G]AAAGTAAAATATCTA | 55819 |
| rs568453543 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015054 | GGAACATATACCTTT[C/T]TACTACCTTACTCAA | 55819 |
| rs568456176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968520 | AAAACACAAAAATTA[G/T]CCAGGTGTGGTGGCA | 55819 |
| rs568462643 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066751 | CTGAGGCAGGAAGGC[A/G]GAACCCGGGAGGTGG | 55819 |
| rs568477274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060030 | AATGTGGGTGACAGA[C/T]GGAGAAAGTCAAAGT | 55819 |
| rs568512196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041103 | CCTGGACTGGGGGCC[A/G]GTGAGGAGGCCAAAA | 55819 |
| rs568530469 | in-del | -/TGTTT | 0.439248 | 0.163356 | intron-variant | RNF130 | GRCh38.p7 | 5:179982576 | TTTTGTGTTTTGTTT[-/TGTTT]TGTTTTGTTTTGTTT | 55819 |
| rs568543670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180002126 | TGGGATGTGTGATCA[C/T]TCTGGATGGCCAATG | 55819 |
| rs568587795 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179925753 | GACCAGGCTGGTTTC[A/C]AATCCCTGGGCTTAA | 55819 |
| rs568603634 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179957939 | CTGGAGTGCAGTGGC[A/G]GGATCTCGGCTCACT | 55819 |
| rs568635820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995739 | GACTGCAGAGGAACA[A/C]TGACTCCCCATCTCC | 55819 |
| rs568650375 | snp | C/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179964049 | CCCAGCCGTCTGCGA[C/G]CCGGCCTCCCATGGC | 55819 |
| rs568653400 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002104 | GGAGCTGCTTCAGCT[C/T]AGGTACTGGGATGTG | 55819 |
| rs568669469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050477 | TCAAACGTTAACCTC[A/G]TCCAAAACCACCCTG | 55819 |
| rs568670582 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023787 | CAAATAATTATGTAG[A/C]TACTCTACCCTAAGG | 55819 |
| rs568681429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950456 | TCGTATTTCTGGTTT[C/T]AGGAACAAAAATACA | 55819 |
| rs568756280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987959 | TGTCTGGTTTTAATA[C/T]TGGAATAATTTGGGT | 55819 |
| rs568757618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051242 | GTATAGATATTATAT[C/T]TATTTATTTATTTAT | 55819 |
| rs568763819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946698 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 55819 |
| rs568792215 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062729 | CAGAGATGAATGTGG[C/T]AGACTTCTGTCACAT | 55819 |
| rs568805980 | snp | C/T | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954790 | TGAACCCGTTTTCAA[C/T]AGGAATACGTTCTCA | 55819 |
| rs568809632 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | RNF130 | GRCh38.p7 | 5:180065135 | GCTACAGAATGAATT[A/T]AAAAAAAAAAAAAAT | 55819 |
| rs568819654 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179988586 | TGTATCTTGTAGGTT[A/T]TGGTATGTTTTATTT | 55819 |
| rs568857374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012721 | AAGTCTCCCTAACCC[C/G]CCTCCAAGTTCCCAT | 55819 |
| rs568870332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965340 | CGGTGCCCAGGGCTT[C/T]GGAGGGAAAGCAGAG | 55819 |
| rs568871490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005137 | CCACTGCTAAAAAAC[C/T]GTACTGATGGCCCGG | 55819 |
| rs568877884 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026268 | CACAAAATTCTTACA[G/T]ACATACAGATAAAAC | 55819 |
| rs568878277 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978604 | CCCATCCCTCATTCC[C/G]CCTGCATTACTTATT | 55819 |
| rs568880095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180057465 | GAGGCAGGAAATTGC[C/T]GGAACCTAGGAGGTG | 55819 |
| rs568888738 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180010141 | AGTCCCAGCTACTCC[A/G/T]GAGGCTGAGGCAGGA | 55819 |
| rs568934500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960200 | AAATTCAGTAACCTC[A/G]CTTACCTAGGTACTA | 55819 |
| rs568937278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179941564 | CTCTCCTTCTCTCTC[A/G]GTCTTTGGGCCATCA | 55819 |
| rs568942074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179966053 | GATGAAAGGAACATG[C/T]AGAGAATGGAAGCGA | 55819 |
| rs568984016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070875 | GTAGTTCCGATTAGT[G/T]TCAGATCCTCATAAT | 55819 |
| rs568995484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953279 | AAATGATCTACATAT[A/G]CAGTGCAATCCCTAT | 55819 |
| rs569003513 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931361 | TGTGAAAACATATTA[C/T]AGTTCTGCACATTTT | 55819 |
| rs569006917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180005853 | GAAATATTTACTGAG[A/G]CAGTGTGATGTGCCA | 55819 |
| rs569020980 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180071441 | ACCGCCCGCCGCCCC[C/G]GGGCCGGCACTCACC | 55819 |
| rs569037276 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179972713 | CCAGATTTTGCTTTG[C/G]CCTTTTCTTATTGTT | 55819 |
| rs569038366 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957998 | TTCTCCTGCCTCAGC[C/T]TCCCAAGTAGCTGGG | 55819 |
| rs569084635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954130 | AAGAAATTGCAACCC[A/G]CATACTCTCTTGGTG | 55819 |
| rs569115668 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929802 | TACACACACCCACAC[A/C]CACCCACTGGGGTGT | 55819 |
| rs569136273 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035985 | TATATTAATTGCTTT[C/G/T]AAGTTTGTCTCTGCT | 55819 |
| rs569144942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065225 | TCCTTTCATGGAAAA[C/T]TTTCCCCTTTCATAG | 55819 |
| rs569159912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179990973 | ATATTGGAATAGCTC[A/G]TGCCCTCGGTCTCTT | 55819 |
| rs569171515 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | RNF130 | GRCh38.p7 | 5:179968052 | TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGCG | 55819 |
| rs569173452 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928357 | ATAATGGATATTTTG[-/T]TTTTTTTTTTCATTT | 55819 |
| rs569199300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180029008 | TTGCAATCACCCTCT[C/T]TTAGGTAGACGAGGA | 55819 |
| rs569214659 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982484 | TTTCCAAACTGGGCA[C/T]ATTATTTTACATTTG | 55819 |
| rs569223021 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179991740 | ACATTACATTTATTG[G/T]GCCCTTTATTTCTAT | 55819 |
| rs569275283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926587 | AGGGAGGTGGAGGTG[A/G]CAGTGAGCCGAGATA | 55819 |
| rs569288081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029962 | CAAGGATTCTCCTGT[C/T]TCAGCCTCCCAAGTA | 55819 |
| rs569295588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179950273 | AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT | 55819 |
| rs569316679 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949906 | CTCACTAGCCTCACG[G/T]GGAAAATGGTATAAT | 55819 |
| rs569319250 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179924536 | GGCGCAGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 55819 |
| rs569329336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180021511 | CAGAACCAATGAGAA[C/T]TCTTCAACATAACAA | 55819 |
| rs569351835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064414 | CTGCCCCAGTCACCC[C/T]ACCTGCCCATAGTCC | 55819 |
| rs569356254 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924243 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 55819 |
| rs569357294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179934191 | CTCGACGTTGGCGCA[C/T]AGCAGCCTGGCGGCA | 55819 |
| rs569361394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179977869 | CAAAAAATAAATAAA[C/T]AAATAAATAAAAGAA | 55819 |
| rs569372208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179945047 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCGCTTGA | 55819 |
| rs569386215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058446 | TGAAATAATCCAGTT[A/G]CAAATTATGAGGAAC | 55819 |
| rs569386810 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073414 | TAGTCGTGGTGATGC[A/G]TGCCTGTAGTCCCAG | 55819 |
| rs569395980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179927138 | TTTGGCAATAAGAAA[A/G]TGGGTCAGAACTTAA | 55819 |
| rs569417414 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961714 | ATGGGAATAAGCAAA[A/C]GAGGTGGCTGTGGGT | 55819 |
| rs569440160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007238 | AAATCCCATCTCTAC[C/T]AAAAATACAAAAATT | 55819 |
| rs569446780 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996262 | TTTTCAGTGAGTTAA[C/T]TGTTGGTGTATATAC | 55819 |
| rs569450393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000047 | GACTTTCATACTCCT[C/G]CATGTTTTCCTGGTA | 55819 |
| rs569458159 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180046204 | CTAAGCCCCTCACTG[A/C]CCGGGGCAGGTGCAG | 55819 |
| rs569492395 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF130 | GRCh38.p7 | 5:179997044 | TCTTGAATCTATGTT[A/G]GTATATGTGTCTGGG | 55819 |
| rs569508362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179974813 | AGAGAACGAGGCCCC[A/G]AGGAAGGGAGAGAGC | 55819 |
| rs569512864 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029957 | GGGTTCAAGGATTCT[C/T]CTGTCTCAGCCTCCC | 55819 |
| rs569535551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007727 | CTAGGAAACAAGCTC[A/G]CAGTTTGTGGCCTGC | 55819 |
| rs569556180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058949 | TACTTACCATGACTT[A/C]ACAGTTAGATGGTCA | 55819 |
| rs569566755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988522 | ATTTCTAATTGTCTG[A/T]TTTAGGCATTCATTG | 55819 |
| rs569594000 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF130 | GRCh38.p7 | 5:180052055 | CTCTCTGTTCTCTTG[A/G]CTCCTATCCATCAAG | 55819 |
| rs569595417 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180040845 | ATGCTCCATGGGACG[A/G]TTACCTATAATGCAA | 55819 |
| rs569607531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033021 | GCTCTGTTGCCCGGC[A/G]AGAATGCAGCAGCAC | 55819 |
| rs569610542 | in-del | -/ACTA | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016556 | CGTCTGGCCGCCAGT[-/ACTA]ACTGTCAGAGATGGC | 55819 |
| rs569621495 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180060090 | TGGGCCAGGGAACAC[A/T]GGCAGCTTCTACAAG | 55819 |
| rs569634150 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938846 | AGGCTGACACCACAT[A/G]GCTCACATTTCAGAC | 55819 |
| rs569652907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938195 | ACTCCTGTGCTCAAG[C/T]AATCCACCCTCCTTG | 55819 |
| rs569682302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944467 | TCTCAATTTATTTTT[C/T]ATTTTTTATTTTTTG | 55819 |
| rs569727061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024700 | AAATGACACCAAACG[C/G]AAACTTGGAAATTCA | 55819 |
| rs569769829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179929930 | ATCTTTAATTTCTCT[C/T]GATAACACATAATTG | 55819 |
| rs569783089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180011775 | GTCTCTTAAAAAAAA[A/G]AAAGTTTTTTAAATT | 55819 |
| rs569783095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068114 | ACTAAACTCTTCCCC[A/G]CCAGCACATCTGCAT | 55819 |
| rs569799737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996536 | TATCATGAAGCCACT[C/T]ATCAAATGCTTTTTC | 55819 |
| rs569863082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989541 | TTTACATAACGTCTG[G/T]TTTATCTGGCATAAG | 55819 |
| rs569863793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060636 | TAACTTGGGGCTTCA[A/G]GAGGCAACTGGCCTC | 55819 |
| rs569863922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010761 | AGGGAGGTGGCTGTG[A/G]TTATAAAAGAGTAGC | 55819 |
| rs569874072 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180060931 | AAAATTAGCTGGGCG[A/T]GGTAGTGGGCGCCTG | 55819 |
| rs569896183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179964240 | GGCGGGCGACTGACC[A/G]GGTACTTGGCCACCA | 55819 |
| rs569899346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180017892 | TCAAAAAATGACAAA[C/T]TACCTGCAGGCTTCA | 55819 |
| rs569906305 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069949 | GAAGCACACGAACAC[A/C/G]GTGGAGGAAGGATCT | 55819 |
| rs569922124 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987695 | AGTGTTGAATTTTAT[C/T]AAACGCCTTTTCTGT | 55819 |
| rs569925025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003638 | AGGTATAAGTGTCTA[A/T]GTATGTGTGTACAAT | 55819 |
| rs569927086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964668 | CATTTTTCTAGAAAA[A/G]CATACTTTTGTTAGA | 55819 |
| rs569931806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180010163 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC | 55819 |
| rs569942146 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034760 | AGTGACTCACTGTGA[A/G]TGTGACTATGTGGTG | 55819 |
| rs569943712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923337 | GGCACCTTTATGGAA[A/G]ATCTATTGATTGTAA | 55819 |
| rs569979067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924030 | TTAACTTTTCTATAT[G/T]AAAAGTCTTCTGCAT | 55819 |
| rs569982029 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180032753 | TGAAACGGAGTGTGT[-/AA]AAGTCCTCTAATGCT | 55819 |
| rs570009005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958054 | GGCTAATTTTTTGTA[C/T]TTTTAGTAGAGACGG | 55819 |
| rs570032958 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005830 | GTAAGCTCATTCTTG[A/C]ATTCATTGAAATATT | 55819 |
| rs570034755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028067 | ATGTTGAGCTGTGCT[A/G]TTTTTTTCCTGTACT | 55819 |
| rs570048544 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF130 | GRCh38.p7 | 5:180055477 | GTGTGTGTGCGCGCG[C/T]GCACGCGTATGTGTC | 55819 |
| rs570103525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180041797 | TCATAAAAGCAAGGC[A/G]AGGTGTGGTGGCTCA | 55819 |
| rs570131325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180042451 | AATTAAACGGGGATA[A/G]AAGCCTATGTCATGA | 55819 |
| rs570143993 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052771 | AATCATAAAATCAGT[A/C]CCTACGGAGGATTAC | 55819 |
| rs570147032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180049020 | AGATGCCTGAATTAC[A/G]TAAGGTTTCTGTTTT | 55819 |
| rs570176469 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179945715 | GGACAATGGAAATTC[A/G]ATTTGCTTTGCCCTA | 55819 |
| rs570178289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952465 | AAGATTTTCCAAAAA[A/C]CAGAAGAGGAAAGAA | 55819 |
| rs570183200 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981740 | CTACAATTTCCCTAG[C/G]TGTTTACAGAATGTC | 55819 |
| rs570197586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180034477 | ATAGACTGCACCAGC[A/G]AATTTCATGGGAAGA | 55819 |
| rs570201369 | in-del | -/CG | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179927403 | GATATGTGCACAAAT[-/CG]CATAAGTATCCAGTT | 55819 |
| rs570259428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000642 | CCTATCTTCAAGTTG[A/G]GAGATTCTTTCTTAC | 55819 |
| rs570277321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931415 | TTAAGTGTAGCTTTT[C/T]TGTTTTTTGTTTTTT | 55819 |
| rs570279073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939463 | CTGAACGTTTTTGTT[C/T]GATGACTTTGCATGC | 55819 |
| rs570342576 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180049814 | TAAGCTTCTTTATAC[-/T]TTTTTTCCCTCTCCT | 55819 |
| rs570374935 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180031499 | TCTCAAAAAAAAAAG[A/T]TAAATTTGGGGGGAG | 55819 |
| rs570376510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069016 | TAAACTCATTAAATC[A/G]AGATTATAATGTAAA | 55819 |
| rs570421223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044898 | CAGCACAGAAGCTGA[C/T]GTTAGAGGGTGCCAA | 55819 |
| rs570423962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179967343 | TTTAAAAGAGTAAAC[C/T]ATTACTTTGCTTCAT | 55819 |
| rs570433258 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023044 | TCTGAGAGTTCAGTG[A/T]GCTGAATAATTAAGT | 55819 |
| rs570438822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961249 | AACATGCACGCACAC[A/C]CACACTCTCTCCATT | 55819 |
| rs570508371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985703 | AATTTCCCTTCCAGG[A/C]TGGTGTTTAGTAGCT | 55819 |
| rs570512050 | in-del | -/TCTC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935708 | TTGTTATTACAGTTT[-/TCTC]TCTATTAGTGTATTA | 55819 |
| rs570542684 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180052801 | CAGAAAAAGAAAGAC[A/T]GAGAGAGATTGCTCA | 55819 |
| rs570551574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179928205 | CTTTCCCTCGGATGA[C/T]GCCTGGGAGTGGGAT | 55819 |
| rs570642965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986264 | TTATGTGTTTTACAA[C/T]GATATGCTAAGTCAT | 55819 |
| rs570662978 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072415 | TAAAATTAAATGTCA[C/T]GAGATTTAACATTCA | 55819 |
| rs570671671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037861 | TAATCACAACATAAA[A/G]CCGTTTCCTATTGCT | 55819 |
| rs570685975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942918 | GTCTTTTCTTCTGGC[C/T]GGGTGCCGTGGCTCA | 55819 |
| rs570706294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948429 | AATCCCAGCACTTTG[C/G]GAGGCTGAGGCGAGC | 55819 |
| rs570723055 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981969 | TGCATATGAAATCTA[C/T]GCTGTTTTCATTACC | 55819 |
| rs570754217 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065465 | ACAAAGAAGTGGTTA[A/T]AGTACAGGCACTAGG | 55819 |
| rs570754510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180054441 | ATGCACATTCCTTTC[A/G]CATCCTCCCTCTCCC | 55819 |
| rs570792720 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015014 | TACAACAGTAAAAGG[A/T]GTTTTATGGAAAATG | 55819 |
| rs570796828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179936175 | CACCCAGGCTGGAGT[A/G]CAGAGGCACGATCAT | 55819 |
| rs570825730 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002201 | GGGAGGCATGATTGC[G/T]CTGAGTGTTCAAGGT | 55819 |
| rs570851137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179973753 | GAAGTTCCCCACTCA[C/T]GTGATAAAAACACAC | 55819 |
| rs570855515 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072853 | CTGCTCTAGTGACTA[C/G]GTGAACTACTCCAGG | 55819 |
| rs570863071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974104 | TGCCATGTAAGAACC[C/T]GGCAAATATAAAAGG | 55819 |
| rs570884111 | in-del | -/AAAT | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179977857 | AGACTCCGTCTCAAA[-/AAAT]AAATAAATAAATAAA | 55819 |
| rs570891038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179968435 | CTGTGGGAGGCCGAG[A/C]AGGGCAGATCACTTG | 55819 |
| rs570911202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059971 | AATAAAGAGATTCTC[C/T]TGGACTGTCTGGGTG | 55819 |
| rs570923860 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015912 | CAACCATCCATTCAA[C/T]AATATTTATTGAGCA | 55819 |
| rs570935969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180008777 | TAATCGCAGCTACTC[A/G]GGAGGCAGAGGTCAG | 55819 |
| rs570941149 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015118 | TACCAGAATACCGAT[C/T]AAAAATCTACAAAAA | 55819 |
| rs570944270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059466 | ATGCAGGAACTTCCT[A/G]TCCTGTCTGGAACTC | 55819 |
| rs570947459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027127 | ATGAAGGGAGGGCAA[A/C]ACTGGCACAGGAGCA | 55819 |
| rs570951352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930550 | CTTTTTCTTGCCATA[C/T]GGTAATGGCTAACAC | 55819 |
| rs570962340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180046125 | GTGCGCGGTGGACCG[C/T]GGCGCGTGCAGGCCC | 55819 |
| rs570966360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963419 | AAAACTGCTCCATGT[A/G]TTTTCCTGGGATCAT | 55819 |
| rs570990369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924283 | GGTGGATCACCTGAG[A/G]TTGGGAGTGCGAGAC | 55819 |
| rs570997562 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958570 | CCTGATCTGAGGTCG[G/T]CCTGTGAACAGGTCT | 55819 |
| rs571001766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179962958 | GACTTATTTTCTCTT[C/T]CTCCTCACAGCTGTC | 55819 |
| rs571028961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925174 | TAGCTCCGGGATGGG[G/T]CTGGTCACCAGAAGG | 55819 |
| rs571029806 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF130 | GRCh38.p7 | 5:179957189 | GGCTGAGGTGGGTGG[A/G]TCACCTGAGGTCAGG | 55819 |
| rs571030645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001501 | TCTACTTTGTAGCTG[C/T]GATTCTATCCCTGGG | 55819 |
| rs571074854 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068722 | CTTCAAAATGAGCCA[C/T]CAGGTTCAACTCTAG | 55819 |
| rs571117211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996565 | TCTGCATCTACTGGC[A/G]TTACCACATGGTTTT | 55819 |
| rs571121073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959179 | AATAAACAGTAGTTA[C/T]TCTCATCTTTGTTAT | 55819 |
| rs571144176 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179994163 | GTCAGGTAGCATGAC[A/G]CCTCCAGTTTTGTTC | 55819 |
| rs571183770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179952703 | GAAAATCAATGTAAT[A/G]CACCACATTCATAGG | 55819 |
| rs571213728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180068201 | CAAACAAAAAGTTAG[C/T]GTGCACACACATAAA | 55819 |
| rs571242206 | snp | C/T | 0.000153961 | 0.00877249 | intron-variant | RNF130 | GRCh38.p7 | 5:179970407 | ATAAAATAGGAAACG[C/T]ACCACAATTCCCAGG | 55819 |
| rs571259518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180062150 | ACCTCTGCCTCCCAG[A/G]TTCAAGCAATTCTCC | 55819 |
| rs571262782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939892 | GAATCAACCTCAAAC[C/G]GATGTCAAAATGCAT | 55819 |
| rs571360363 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972938 | TACTAAACAATTAAA[A/G]ATTTCTCCTCTAGGC | 55819 |
| rs571390937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012564 | GACAGACATCTTCTA[C/T]TGGTCTTCCCCCACT | 55819 |
| rs571426065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964052 | AGCCGTCTGCGAGCC[A/G]GCCTCCCATGGCATC | 55819 |
| rs571427134 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179965976 | GTGCTAGGCAAGCAG[C/G]AGCAGGTGCTGGGAA | 55819 |
| rs571429993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050279 | GCCGATGGAGTTCCA[A/G]GCCAAAGACCAGCAG | 55819 |
| rs571436607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179976517 | TTTCCTTTAGCCTCA[C/T]GTTTAGACCGTCAAT | 55819 |
| rs571487698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938940 | AGGATCAAAAGTGCA[A/T]ACACAGGCCGGGCAC | 55819 |
| rs571521787 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967273 | AGAGAAGACTGGTCA[C/T]GGCCCACAGGCACAG | 55819 |
| rs571528241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972646 | GGGACCTGGTAAAGC[C/T]GCAGCACCACCTGGG | 55819 |
| rs571535845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180043473 | ATGTGAGCTACCCCA[C/T]GCTCAGCAGCACCCC | 55819 |
| rs571548703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997394 | ACTGGCGCAATCTCG[C/G]CTCACTGCAACCTCC | 55819 |
| rs571560434 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989888 | ATTGTTTTATGAGAC[-/TT]ATTAATTTTATACTT | 55819 |
| rs571569535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983488 | GACACTATTGTACCA[C/T]GCATCTATTTGTTTA | 55819 |
| rs571590830 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941890 | AATACTGAAACTGAT[C/T]AACGGAATTTAAAAA | 55819 |
| rs571610844 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180005135 | TCCACTGCTAAAAAA[-/C]CCGTACTGATGGCCC | 55819 |
| rs571611048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940608 | TAAAAACTTTAAAAA[C/T]TGAGATAAAGTATCT | 55819 |
| rs571634248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179991608 | GTTGTGGGATGTTTT[C/T]CTTCCACTTGATCTA | 55819 |
| rs571677552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986449 | ATTCAAGATTCATGA[C/T]ACTGCACTAAACACA | 55819 |
| rs571709884 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988395 | TTTAGTCTCTGTTTC[A/C]TTTAGTTCTATGCTG | 55819 |
| rs571721574 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179964945 | TACCTGTAATGTTTT[-/AA]GTTAGGGAAAATGTA | 55819 |
| rs571724745 | in-del | -/GTAC | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179969954 | CAAGATCGTGCCATT[-/GTAC]TCCAGCTTGGGCAAC | 55819 |
| rs571738651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070663 | CCAAAAAATCATATT[C/T]CACGATGTGCAAAAG | 55819 |
| rs571771795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932472 | ACCATATTGGTCAGG[C/T]TGGTCTCAAACTCCT | 55819 |
| rs571777291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063526 | GAGATGTCTTTGTGA[C/T]ACTGAAGTAAAGATA | 55819 |
| rs571790334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979096 | GGCCCGGGATACAAA[C/G]TCAGATGGGTAGGTT | 55819 |
| rs571792342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180028858 | AGAAAAAGTATACTT[A/C]GAAATTTTTTTAAAG | 55819 |
| rs571798633 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180034941 | TGGTAAACTGTCTTC[C/T]TTTTTATTGTTGGTC | 55819 |
| rs571827054 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180033572 | GTGTGCGCCTATAAT[-/C]CCAGCTGCTCGGGAG | 55819 |
| rs571839500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180071342 | GACCCTGGCTGGGGC[C/T]GTCGGCCGGGCAGCG | 55819 |
| rs571910296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933146 | GTTCTCCTCTTTTTC[C/T]AGTCTCAGGACAAAT | 55819 |
| rs571915271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014301 | GGAAATAACTTCCCA[C/T]TGTCTTTTAAGGAAA | 55819 |
| rs571925423 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180064139 | TTAAGCCTATTTATG[G/T]AATAAAATCAATTTA | 55819 |
| rs571930296 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179948627 | AGTGAGCCGAGATCA[C/T]GCCACTGCATTCCAG | 55819 |
| rs571933227 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179988012 | TTCTCTCTTCTTTCA[-/T]TTTTTTGAAATAGTT | 55819 |
| rs571949213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179926529 | TGGCGCATGCCTGTA[A/G]TCCCAGTTACTCGGG | 55819 |
| rs571972977 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010058 | CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 55819 |
| rs571987569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927025 | TGACTGTTATGGGGT[A/G]AGAACAGAGGAAAAA | 55819 |
| rs571991127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179942598 | AGGGAATTGTTGATG[C/T]GGATGCAAAAAGAGA | 55819 |
| rs571991594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943095 | AGCTACTCAGGAGGC[G/T]GAGGTAGGAGAATTG | 55819 |
| rs572004914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009011 | GAATGAAAATGAAAA[C/T]ACAGCATATCAAAAT | 55819 |
| rs572050835 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072957 | CGACTCTCATTTTCT[C/G]TCTCCATGGCGTTTA | 55819 |
| rs572055263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180038175 | TCCTCTCACCCAAGC[C/T]GCCCAAGCAGCTGGG | 55819 |
| rs572057353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030503 | AGAAAATTCACTCAC[A/G]CCGTTTTTAAAAATA | 55819 |
| rs572068396 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180023217 | TCAATGCAGATGATT[A/T]CAGATAGAAATATTT | 55819 |
| rs572069070 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180023876 | TTATCATATGGCAGG[A/G]GGAAAAGAGTTAACT | 55819 |
| rs572074522 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072585 | CCAGGGACTGAGGGA[A/G]TTGAAGTGGTTTCCG | 55819 |
| rs572103087 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974222 | CAGTGGAGCCTCAGA[C/T]ATCTGCAGCGGCCGG | 55819 |
| rs572116290 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180039454 | TGTCGGCCAGGGTGG[G/T]TTCAAACTCCTGACC | 55819 |
| rs572118336 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179960122 | TTTCAGTTGGTAAAT[C/G]TTGACATTTCACAAG | 55819 |
| rs572120665 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180031072 | CAGTAAATATATTTT[C/G]TCTTCCTTATGATTT | 55819 |
| rs572138903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179935538 | TGTGTGTGTGTATAC[A/C]TTTTAAATCTATCTT | 55819 |
| rs572151915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179973916 | TACTTGGGGATACAG[A/G]ACGAGAAACAAATAG | 55819 |
| rs572174043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065629 | GCTGGGTGTGGTGGT[A/G]GGCACCTGTAATCCC | 55819 |
| rs572180819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016100 | CCGGGCAGAGGAGCC[C/T]GACCCTGCCGATCGG | 55819 |
| rs572219056 | in-del | -/G | 0.0152066 | 0.0858606 | intron-variant | RNF130 | GRCh38.p7 | 5:179944158 | TTTTTAGTAGAGACG[-/G]GGGGGGTTCACCATA | 55819 |
| rs572225744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922405 | GCAACCTCCACCTCC[C/T]GGGTTCAAGAGATTC | 55819 |
| rs572241809 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942963 | GCAATTTGAGAGGCC[A/G]AGGAGGGTGGATCAT | 55819 |
| rs572247071 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179921913 | TGTAATCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 55819 |
| rs572262377 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066225 | CATACTATTCTCGTG[A/G]TAGTGAATAAGTCTC | 55819 |
| rs572262456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059163 | TACATCACAGTTTTT[A/G]CACCTTTTAGTCTTC | 55819 |
| rs572287115 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988838 | TGTTCCATATGTTGA[A/G]GAAAATGTGTATTCT | 55819 |
| rs572288166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180032597 | TGTTGAAAGACTGTC[C/T]TTCCCTCACTGAATG | 55819 |
| rs572293034 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179962650 | GCAAAAATAAAAAAA[A/C]CCTTTCTATACCTTA | 55819 |
| rs572312848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929040 | TGAAGAAGTCTTTGC[C/T]TATCTGAAGGTTTTG | 55819 |
| rs572352989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033471 | GCTCATGCCTGTAAT[C/T]GCAACACTTTGGAAG | 55819 |
| rs572369339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179929999 | TATTCCTCAGTATGA[A/T]GTTTCTTTGATGCTT | 55819 |
| rs572369657 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179938540 | TAAATTGTTCACTTA[C/T]TTATTCATTTATTTT | 55819 |
| rs572370909 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966077 | GAAGCGAAGAGAAGA[A/G]CTGGCTTGTTGAGGG | 55819 |
| rs572375571 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179994374 | CCATTTGTTTGTGTC[C/T]TCTTTTATTTCGTTG | 55819 |
| rs572390373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046605 | TCAAAACAGGCGGCC[G/T]CACAGCACAGTGGCA | 55819 |
| rs572399841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180046166 | GGGACCCAGCGCACC[C/T]TCCGCAGCTGCTGGC | 55819 |
| rs572405036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179963075 | CCGCCGGGGCTTCCC[C/T]AGAAGCTAGACATGC | 55819 |
| rs572425483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180054807 | TAACAAAACAAGTCT[G/T]TGGACCTATGAACAT | 55819 |
| rs572431511 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962210 | TCCTCTGAAGGCTGG[A/C/G]GAATGCCACCCGACC | 55819 |
| rs572470357 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179956635 | GATCCTGCTCTGTGC[A/G]GTCCTCACTGTGTGC | 55819 |
| rs572475910 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF130 | GRCh38.p7 | 5:179944132 | GCCTGCCACCATGCC[C/T]AGCTTTTTGTATTTT | 55819 |
| rs572480844 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179950633 | TTCCCTAAGACTGAT[-/G]GGAAGTCCCAATCTA | 55819 |
| rs572483247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987299 | CAGCCTCCTGAATAC[C/T]TGGGACTATAGGCAC | 55819 |
| rs572484049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179957348 | ACCTGGGAGGCAGAA[A/G]TTGCAGTGAGCCGAG | 55819 |
| rs572490945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179988171 | GGTTCAATGTTGGTA[A/G]GTTGTATGTGGCTAG | 55819 |
| rs572515392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180042949 | GACTGAAATTCTCCC[A/G]TCTTTAATTTGTACT | 55819 |
| rs572517269 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948652 | TTCCAGCCTGGATGA[C/T]AGATAGAGCGAGACT | 55819 |
| rs572585452 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073706 | ATTTACTTATCCTCG[A/G]CAAGTACAGACCCTA | 55819 |
| rs572627485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980852 | CAGACACTGCTAGCA[A/C]TGCTTGGCACCAACA | 55819 |
| rs572643821 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180024925 | GGAAGCCCTGTGGGA[A/G]GGGTCTCCATGCTGT | 55819 |
| rs572653625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180067894 | GAATTTCTAAAAACC[A/G]ATTTCAGATTCATTA | 55819 |
| rs572662204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017170 | AAAGAGTCCAATCCA[A/G]ATGTTCTGACCATGC | 55819 |
| rs572667050 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046523 | TTTCCTTCCTACCCC[C/T]GAGAATTGTCAGTCT | 55819 |
| rs572675872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180018130 | CGAAACCCCATCTCT[A/C]CTAAAAATACAAAAA | 55819 |
| rs572695885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974621 | ACGAGGGTGTCCAGG[C/T]CCATCTCCCTCCCTC | 55819 |
| rs572725353 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934046 | GTGACGATCAGATTT[C/T]AGATTTGCCAGTGGA | 55819 |
| rs572727207 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179969277 | GCTGGACTCTGGCAC[A/G]CCTGGCGACAGCCCC | 55819 |
| rs572746645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940791 | TCTCTTCAAATACTG[C/T]TTCTGCCCCATTCTC | 55819 |
| rs572750624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036082 | AACATCTCTATATTT[A/T]GCATGTCTTATAATC | 55819 |
| rs572751614 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057506 | TGAGCCAAGACCGTA[A/C]CACTGCGCTCCAGCC | 55819 |
| rs572758756 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179941708 | ATCACTGCACTGATA[C/G]CTCTTTAATTTCTTA | 55819 |
| rs572781698 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179997545 | GTGTTAGCCAGGATG[G/T]TCTTGATCTCCTGAC | 55819 |
| rs572787312 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925560 | TTGAGGTGCTCTCAC[C/T]CTGTTGCCCAAGCTG | 55819 |
| rs572807822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933682 | ACGCTCCACCATGCC[A/G]GGCTAATTTTTTCTA | 55819 |
| rs572821826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179974912 | GGTCAGCACGCTGAG[A/G]GAATTAAACCCATTG | 55819 |
| rs572823166 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RNF130 | GRCh38.p7 | 5:179946589 | GACGGAGTCTCGCTC[A/T]GTCGCCCAGGCTGGA | 55819 |
| rs572834959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180050616 | CACTTTTTTCCTTCT[C/G]TGTTCCATTTCCCTC | 55819 |
| rs572867563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179953480 | ATAAACTCATATGTC[A/G]TTCTCAATTGATTTT | 55819 |
| rs572870980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959553 | AATTTCTTGAACCCG[A/G]GAGGTGGAGGTTGTG | 55819 |
| rs572885072 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179960281 | ATTCACTTCTTTGAC[A/T]ACCATCCTGTTTATA | 55819 |
| rs572886052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179998363 | AGCACGTTTGTAAAT[G/T]TCCATGTATTTGTAC | 55819 |
| rs572892093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179973633 | TCCCGCACGCCTGAC[C/T]GCGCTCACCCTCACT | 55819 |
| rs572929611 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054124 | CGGCCAGCAAATACA[A/T]TCTTAGAATAGGTTT | 55819 |
| rs572975356 | in-del | -/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071711 | GCTCATCGTCCCTCC[-/G]GGCAGCCGCCGCTGC | 55819 |
| rs572976434 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946714 | GCCCGCCACCACGCC[A/C]GGCTAATTTTTTTGT | 55819 |
| rs573014548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020965 | GATTTAAGTCTTAGG[C/T]CTTCCTTCCTTAAAA | 55819 |
| rs573020775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180070386 | AAAAGCCTTATGTGA[C/T]TATTTTTCCCCAGCC | 55819 |
| rs573038006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961243 | ATACACAACATGCAC[A/G]CACACACACACTCTC | 55819 |
| rs573045661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983889 | AGAATTTCCTATTTG[G/T]TGATGCTATGGAAAA | 55819 |
| rs573095313 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923237 | AAATAAGAGTTGAAG[C/T]TCATTTTTTTTTTTG | 55819 |
| rs573095351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961847 | AGACAATAAAGGCAG[A/G]TGGTCATCTGACTCA | 55819 |
| rs573096078 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067088 | TTATTCAAGGCGGGA[C/G]GGATCTCAGAAGTTA | 55819 |
| rs573098444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179972202 | GGTCAAGTGCACTAA[C/T]GCTGGCTACTGACCA | 55819 |
| rs573130045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925411 | CACTGAACTCCAAGC[C/T]GCTTCTCACATGCCT | 55819 |
| rs573134976 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954254 | CCTAGGGACATATCA[A/G]AGAGAACTGAAAATA | 55819 |
| rs573158677 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063439 | ATTGAGATGGGAAAG[A/G]CTGGAGAGCAGTGGT | 55819 |
| rs573159000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179976788 | GGAGATAACAACTCA[C/T]AATTATTTTATTAAT | 55819 |
| rs573206762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179985949 | TGCTACTTCTTGATC[A/G]TCAAAAGCTACTTCT | 55819 |
| rs573209518 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | RNF130 | GRCh38.p7 | 5:179966977 | TGAGCCTTTCCATAT[C/T]GAATGCTACGTTATC | 55819 |
| rs573233016 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948986 | TTTTTTTTTTTTTGA[C/G]ATGGAGTCTCGCTCT | 55819 |
| rs573237486 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061047 | CTGCACTCCAGCCTG[A/G]GCGACAGCGAGACTC | 55819 |
| rs573271993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180051632 | GGAATGTCCTAACAG[G/T]GGAACTGCAGCAGAT | 55819 |
| rs573277898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179920830 | GTTTTGCTTTTGTTG[C/G]CCAGACTGGAGTGCA | 55819 |
| rs573291100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180066968 | CCCGAGGTCAAGGCT[A/G]CAGTGAGCTATGACC | 55819 |
| rs573308393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014005 | AGGCTCCTTGCTAGT[C/T]TACCCCAGAACTCTT | 55819 |
| rs573317372 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971067 | AAGTAACACTCAGCA[A/T]TTTTCAGCTGAAATG | 55819 |
| rs573328596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180014374 | AGCTGAAGCTGCCGG[G/T]GGCAACATGTAGCTT | 55819 |
| rs573354106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179992369 | GATGAGTCTCGATCT[A/C]CTGACCTCGTGATCC | 55819 |
| rs573391114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180007304 | TACGTGTGAGGCTGA[A/G]GCAGGAGAATTGCTT | 55819 |
| rs573414048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180000126 | TTCTCAATTTTTGTC[C/T]AGGAAAGACTATTTC | 55819 |
| rs573417037 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:180060721 | AAAGGTACACCGCTT[C/T]CATCACTTATCAAAG | 55819 |
| rs573430952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180045655 | GGTGCTGACTGGTGC[A/G]TTTACAAACCTTGAG | 55819 |
| rs573435286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963858 | CGGTGAAAATATGTA[C/T]ATAAAATTGCACAAG | 55819 |
| rs573441350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179990535 | GGCCTGACATCAGTC[A/G]GGCCTTCCACAAGAG | 55819 |
| rs573454772 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179948204 | ATATCTTCTCTCATT[C/G]AGATATTGCGAAGAT | 55819 |
| rs573475341 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179992732 | TTTTATGGTTTATTT[A/T]TTATTATTATACTTT | 55819 |
| rs573504990 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018633 | TTGTATTATTACTCA[A/C]AGAAAGCAAAAGAAA | 55819 |
| rs573532480 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946679 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55819 |
| rs573550479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037324 | CCGCTGGCTCTCACA[C/T]GGTTGGAGGTGAAAT | 55819 |
| rs573568641 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016047 | ACTAGGAAGAGAAGC[C/T]GCTCGCGGTGGCGTC | 55819 |
| rs573569880 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921119 | TTTTAAGCTTTACTG[G/T]GGTATAACTGACATA | 55819 |
| rs573608929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060236 | TGTAAGAGGAGTAAA[C/T]TGGTGTTGCTGTGAG | 55819 |
| rs573627238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922600 | AGGCACAAACCACCA[C/T]GCCCGGCTTGGGCTG | 55819 |
| rs573696553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180002469 | TCCAATTCCAAGATG[A/G]TATAGCACAGCAGCT | 55819 |
| rs573705863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180055749 | AAACTGGTAGAGCTG[A/G]TACTTCTCTCTTTTT | 55819 |
| rs573721671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017020 | TTAATAGCTGTTTAA[C/T]TTGTTTAGTTTTGTG | 55819 |
| rs573734024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180009960 | ATAACAACTTGAAAG[C/T]ATCTTGGCCGGGCGC | 55819 |
| rs573762451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958090 | CACTGTTTTAGCCGG[A/G]ATGGTCTCGATCTCC | 55819 |
| rs573781438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981852 | GAGTCCCTTCTGTCA[C/T]GCTGGTTTTAAACCA | 55819 |
| rs573784937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003211 | CTCATGACTGACATG[C/G]AGGCACGAAGAGGGG | 55819 |
| rs573793004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180047705 | GCCGAGATTGCACCA[C/T]TCCACTCCAGCCTGG | 55819 |
| rs573798084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010189 | GAGGCGGAGCTTGCA[C/G]TAAGCTGAGATCCAG | 55819 |
| rs573809027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995411 | AGCTGTACTCATTTA[C/T]CATTTCTGGCTGTGT | 55819 |
| rs573823699 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF130 | GRCh38.p7 | 5:179951363 | TCTACAGAACAGTCC[A/G]TCCAACAAGAGCAGA | 55819 |
| rs573842317 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921003 | TTTCCATTGCCCCAA[A/T]ATAATTATATTTTGA | 55819 |
| rs573868711 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948410 | TGCATTGGCTCATGC[C/G]TGTAATCCCAGCACT | 55819 |
| rs573964056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180033538 | AGACCAGCCCGGCCA[A/G]CATGGTGAAACCATG | 55819 |
| rs574015010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026736 | TATAAAACATAGCCT[C/T]AAATGAAAAGAAAGC | 55819 |
| rs574021684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179945784 | TACTACGCGCCGCTG[C/T]AGGAAACTCTGTCAT | 55819 |
| rs574044352 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059061 | TAAAGTCCAAAATCC[C/T]AACAAGGCCTGGAAA | 55819 |
| rs574057791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930925 | TGCATGACTGTAGTT[C/T]CAGCTACTGGGGAGG | 55819 |
| rs574059246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179992595 | TTACTGTGTTTTTTT[G/T]GGGGGGTGTCATATT | 55819 |
| rs574062343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975040 | TGCTGTGCCGAATGC[A/G]GAGCGCCAGCCAGGC | 55819 |
| rs574064881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179945309 | AACAGTGGGACCCAA[G/T]GGACCCAAACGCTGC | 55819 |
| rs574069420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179984857 | GTGCCAACATGAAAC[C/T]CAATGGAAATGCTCA | 55819 |
| rs574071131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180041851 | GGAAGCCGAGGCAGG[C/T]AGATTGCTTGAGCCC | 55819 |
| rs574083652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034065 | ATGCCCTTTATCAGG[C/T]TGAGGATATTTCCTA | 55819 |
| rs574126191 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013448 | CCACTTCTCAACTGA[A/C]ATGTAGATGCAGCTG | 55819 |
| rs574130308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180019221 | AACCCCATCTCTACT[A/G]AAAATACAAAAAATT | 55819 |
| rs574137314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179975964 | TGCCCGGCCTCCACC[A/C]GGGATGCTTCTGAAA | 55819 |
| rs574150540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179939627 | GCCATTCCACTACCA[C/T]AAATGACGTGGAAGA | 55819 |
| rs574181205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179985831 | GTCCTTTGTGGCACT[C/T]TCCCCCCAAATAGGG | 55819 |
| rs574197880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179924602 | CAGGAGGAGTTCGAG[A/C]CCAGCCTGGCCAACA | 55819 |
| rs574204480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180056557 | AGGTGGTGTTACCGA[C/T]AGACAGCAAACACTA | 55819 |
| rs574213962 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965651 | CCATAAAACCTCAAC[A/G]CCAAAGTAAGAAAAC | 55819 |
| rs574215221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180019974 | CAATCTGGGCAGGAC[A/G]GAGAGGTGAAGCCAG | 55819 |
| rs574266981 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF130 | GRCh38.p7 | 5:180057289 | CACAGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 55819 |
| rs574272738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069162 | ATTTAGATTTCATAT[A/G]AACCCATAGGTTTAG | 55819 |
| rs574291471 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180055126 | GGCGGGCAGATCTCA[C/T]GAGGCCAGGAATTTG | 55819 |
| rs574309239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965072 | TATGCAGACTACCTT[A/G]TAGAACTTCGTCACA | 55819 |
| rs574334502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014527 | CATATCAATGTAAAC[A/C]AACAAAACAATCAAG | 55819 |
| rs574340663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036357 | GTCACTGGCTCTCCT[C/T]TGCTAGCCCACCTCT | 55819 |
| rs574348925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015242 | AAATAATGCTAAACC[A/G]CTTTAAATTTCCCTT | 55819 |
| rs574351664 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930048 | TTGAAAATTTCATTT[C/T]ATTTATTTATCTTTT | 55819 |
| rs574377339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180037240 | TCCATGCACATGTGC[A/G]AGAGTAACAAGGGTG | 55819 |
| rs574395023 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017178 | CAATCCAGATGTTCT[A/G]ACCATGCCCCTCAAT | 55819 |
| rs574418180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179958959 | GCGCTGGGATTATAG[A/G]TGTTAGCTACCACGC | 55819 |
| rs574420939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933929 | GGGAGCAGACTGTTC[C/T]GCCATTTTTTCTAGA | 55819 |
| rs574427017 | snp | A/C | 0.00478085 | 0.0486577 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072904 | GCAGTGGGAACCCCC[A/C]CTCCACCTTCCGAAA | 55819 |
| rs574432632 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060886 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 55819 |
| rs574435744 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977701 | TACTAAAAATACAAA[A/C]ATTATCTGGGCATGG | 55819 |
| rs574437873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180030290 | CTTGAGGACATACAA[C/T]TGAAACCTGTTTCAG | 55819 |
| rs574448702 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180048501 | AATGAGGCCAGGTGC[A/G]GTGGCTCATGCCTGT | 55819 |
| rs574464422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947394 | AGCCCAGCACACTTC[C/T]TGGCCTTTTCTACTA | 55819 |
| rs574474859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044941 | TTAAGAGACTGAAGG[A/G]GGGAGGAGGGCAGGA | 55819 |
| rs574503118 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922585 | AAGTGCTGGGATTAT[A/G]GGCACAAACCACCAC | 55819 |
| rs574524354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179978112 | CCACGAGGTGGGTGG[C/T]GCTCAAAAGCAAGGG | 55819 |
| rs574525934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947963 | CCATTCACTTCCCCC[A/G]TTTTCACCCTGAGAC | 55819 |
| rs574526180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179941894 | CTGAAACTGATTAAC[A/G]GAATTTAAAAAATGA | 55819 |
| rs574538448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179942525 | AAAATAGTAAGTGGA[A/G]GCCCAGCTGAGCCTT | 55819 |
| rs574572029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180058724 | CCACGCCTGGCTAAC[A/G]CTAATTTTTGTATTT | 55819 |
| rs574587793 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180072079 | GGAAGCGCCCCGAGG[A/C]GGGTCAGCGGAACAC | 55819 |
| rs574600435 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180007426 | AACAAAAACAGTTTG[C/T]GAGAGAAAATCAGAG | 55819 |
| rs574601324 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003009 | AGAATTCTACCAAAG[A/G]GTTCTGAACAGAAAA | 55819 |
| rs574613619 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952745 | TAAAGGGCAAACTCA[C/T]ATGATCATCCCAATA | 55819 |
| rs574617644 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180046130 | CGGTGGACCGCGGCG[C/T]GTGCAGGCCCACAGT | 55819 |
| rs574619278 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180038403 | GGGAAAAAAAAAAAG[C/G]CTGTTTTGTTTTTTT | 55819 |
| rs574620664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179927627 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGACTG | 55819 |
| rs574672813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943409 | TGGGATCAGGGAGGG[C/G]CTGACGTGGACTTTC | 55819 |
| rs574674933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180064999 | TTTGGACCAAGTTGT[C/T]TTGGTCCTAGAGTGC | 55819 |
| rs574675233 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072527 | GGTAGCCGTCCCTAA[A/C]CATTTTGGCACTGGG | 55819 |
| rs574684898 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180055773 | TCTTTTTAGCTACTA[C/T]AAAGGGTTAAAAAAC | 55819 |
| rs574712383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180065559 | AGGTCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 55819 |
| rs574745920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179944538 | CCACAATCTTGGCTC[A/G]CTGCAACCTCCACCT | 55819 |
| rs574751187 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021336 | CGTGGTTCTCTCCTC[C/T]GGAAAAACACCACTG | 55819 |
| rs574760381 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073047 | TTCAGGAACTTACAG[C/G]ATCTTTGTGGGGAGG | 55819 |
| rs574775811 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180053126 | CATGCCGAGGTCAAC[A/T]GGCCAAATGGAGTAA | 55819 |
| rs574777447 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180053866 | ACAGAGTCTCACTCT[G/T]TCGCCCAGGCTGGAG | 55819 |
| rs574780058 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179955919 | AGGTCAGGCCCATGG[C/T]GTGTTGTTTAAATAC | 55819 |
| rs574804232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180000973 | CTGTGTTGATGTCTG[C/T]GCATCTGGTGGAACA | 55819 |
| rs574805516 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:179956597 | ACCACCTACAGCAGA[C/T]ACACCAAACCACACA | 55819 |
| rs574826965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001777 | GGACCCAGCATGGGA[G/T]GGGAGGATAGCACAG | 55819 |
| rs574866034 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927743 | AGGTGCCCGCCACCA[A/C]GCCTGGCTAATTTTT | 55819 |
| rs574871737 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974487 | TGTCCACAGTAAATA[C/G]TGCGACAGAAGAGGA | 55819 |
| rs574897030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179925860 | AGCCAAGTTGGAAGA[C/T]GTAGGCCCAGAACAC | 55819 |
| rs574916635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179949649 | ATTCAACTTTATACA[C/T]TGCTTCTATTTGTAA | 55819 |
| rs574929894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180048500 | TAATGAGGCCAGGTG[C/T]GGTGGCTCATGCCTG | 55819 |
| rs574977025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993765 | TTGGCTTTTGTGGCC[A/G]TTGCTTTTGGTGTTT | 55819 |
| rs574978882 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031858 | GGTTGTACCATTTCA[C/G]ATTTCTACTCGCAAT | 55819 |
| rs574992778 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180010027 | CTGAGGTGGGCGGAT[C/G]ACAAGGTCAGGAGAT | 55819 |
| rs574995648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986569 | TGACATTTCAAGTGG[A/G]CACTGGCAACACTGG | 55819 |
| rs575032421 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944157 | ATTTTTAGTAGAGAC[-/G]GGGGGGGTTCACCAT | 55819 |
| rs575073467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179946003 | TGAGTGACAGAAGCA[C/T]ATGACTGACGTTCCT | 55819 |
| rs575115931 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998353 | GTTGTTTAGGAGCAC[A/G]TTTGTAAATTTCCAT | 55819 |
| rs575123906 | snp | A/G | 0 | 0 | intron-variant | RNF130 | GRCh38.p7 | 5:179964836 | CACCAGTGCAGCCAC[A/G]GCCTCTCAAATTACA | 55819 |
| rs575139991 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952516 | ATGCCAGCATTACAA[-/T]TAATACCAAGGTCAG | 55819 |
| rs575158658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180003843 | ACTGTTTTTCAAGGT[G/T]TGGTCCATGGGGCAG | 55819 |
| rs575184660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179940704 | TTTTTTTTTCACTCT[A/G]CTTGGTGTTCCCAGT | 55819 |
| rs575192731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069248 | AGAGACGGATTTTTT[A/T]AAATCTGTTTTGTTC | 55819 |
| rs575193955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179971486 | ACCATTCTCCTGCCT[C/T]AGCCTCACAAGCAGC | 55819 |
| rs575211346 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966345 | AAATAAAGTGCGCAA[C/T]AGGCTATGTTCCAAG | 55819 |
| rs575218897 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180070246 | AAAAGTTGTTTCTAC[G/T]GCCAAGCTGGGACCC | 55819 |
| rs575251219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179972118 | TATGTCTTGTTACTC[A/G]TAGCCTCTGTGTGTG | 55819 |
| rs575272610 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070487 | GTTAGTATCTTAAGA[C/G]TGTACAAGCAAATCA | 55819 |
| rs575290212 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950914 | GAAGAATTGCTTTGA[C/T]CTCCACTGAGATGAA | 55819 |
| rs575316206 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050403 | ATTCATGCCATCAGT[A/G]GAATGGATAAGACCC | 55819 |
| rs575347258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034819 | TGAACCTGTGGATGG[C/T]CATGGGGACCCCAGA | 55819 |
| rs575367118 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930658 | CACTGATAAGTATAA[C/T]GTTTGCTGTAGTTTT | 55819 |
| rs575367266 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024616 | AAAAAAGACACTTTC[A/G]GATAAATAAATGTTG | 55819 |
| rs575403104 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179940308 | TCACTGCAACTTCCG[A/C]TTCCCAGGTTCAAGC | 55819 |
| rs575412786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179989940 | AAATATCAACCTTTT[A/G]TTTCCATGTCTGGGA | 55819 |
| rs575412795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179997487 | CACCACCACACCCGG[C/G]TAATTTATTTATTAT | 55819 |
| rs575415839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180027672 | TAGCAGCCAGGACGC[A/G]TGCCTTCCTGCTCCA | 55819 |
| rs575458741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179931754 | CACTCCAGCCTGGGC[A/G]ACAGAGCCAGACTCT | 55819 |
| rs575459902 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972144 | GTGTGGAGTGGTTCC[G/T]TACTCCAGGGTGTCC | 55819 |
| rs575462962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180035346 | TTCCCAGCTTTTCTT[C/T]AGTTGTGGTTGAAGA | 55819 |
| rs575473679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179990467 | ACCAGGGGCGTGACC[A/G]CTGAAGCACAGCATC | 55819 |
| rs575474846 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020376 | GTGAAGTCTCCCCAC[A/G]TGGAAGTGACTGGTG | 55819 |
| rs575479290 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048300 | CTGTAGTCCGGTTTA[C/T]GGCAAATCACTCTGT | 55819 |
| rs575520142 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974883 | GCAGACGGCCTCTCC[A/G]GCCTGCGCACCCGGG | 55819 |
| rs575532201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179983670 | TTTGTCCATCTCTAT[A/G]ATAAAAGACATCAGG | 55819 |
| rs575562963 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044426 | TTACCTCTTGACAGG[A/C]ACCAAACAATTCTGG | 55819 |
| rs575565653 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962252 | GAGCCTCAACATGTA[A/T]GGCTCACAGATGCCA | 55819 |
| rs575603124 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945443 | TTCATCTTTTCATAC[A/C]AGGAAAGAGAAAACA | 55819 |
| rs575613484 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072986 | TAAAAGATACACATC[A/G]CTATAAAGTATCAGC | 55819 |
| rs575623020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180063065 | TGGAGCTAGACCAGG[C/T]AGTGAACACCTCATA | 55819 |
| rs575640664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179932592 | AAAACATTTACGTCT[A/G]TTTGGGAGGCCGAGA | 55819 |
| rs575646139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179974246 | CGGCCGGCCCCCCGC[C/T]TTAGCTCCTGAAGTG | 55819 |
| rs575676915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180066201 | TGGAATCATGGAGGC[A/G]GTTTCCCCCATACTA | 55819 |
| rs575692721 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063568 | CCAAGCGCATGAACC[C/T]AGAGAGGCCTAGGCT | 55819 |
| rs575718255 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056317 | TGCATACCCTGGGGC[C/T]ACATGTGGATGTGCA | 55819 |
| rs575748087 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973374 | TCCTGCTAGTCTCTT[C/T]AGTGCAACTTTCACT | 55819 |
| rs575752186 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180020888 | CAACTTTCAACACAA[C/T]ACAGGAACTCCCACA | 55819 |
| rs575760349 | snp | C/T | 0.00023062 | 0.0107358 | missense | RNF130 | GRCh38.p7 | 5:180013203 | TTCTTCGGTGGCATT[C/T]GAGTTCCAACAGCTA | 55819 |
| rs575766213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179951422 | GGAGTCTCGCTTTGT[C/T]GCCCAGGCTGGAGTG | 55819 |
| rs575768050 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973694 | CCATGGACACCCAGG[-/A]AGGCCTCAGAAAGAG | 55819 |
| rs575776498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179998697 | AGCTGTTGGATGAAA[C/T]ATATTGTAAATGTGT | 55819 |
| rs575782364 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053869 | GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTAC | 55819 |
| rs575791141 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922728 | GGCTTCAGCTCAGGA[C/G]TTCAAGACTAGCCTA | 55819 |
| rs575794350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057964 | CCCTTTACCTGTGGG[A/G]TCTGCGCTAACTTTA | 55819 |
| rs575798480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179961123 | TGTTAAAAAAAAAAA[A/C]CACAACACATAAAAG | 55819 |
| rs575820615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180006369 | TTTTAACCTTTCTCT[C/G]ACACAGGAATGTTCC | 55819 |
| rs575821849 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180013838 | AACTAGTGCCAGGAA[A/C]AAAAACAAGTACAGG | 55819 |
| rs575858238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180001886 | GGTACTAGAGTTCTA[C/T]GGCCTGTAAGGGCAA | 55819 |
| rs575859864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179954454 | GAACACATGCTAAGT[A/C]AAAGACGCCAGACAC | 55819 |
| rs575868583 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920038 | CATTAATCCTGGGCC[C/T]GGCCTCTTCTCTGGA | 55819 |
| rs575899674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979871 | TAGGAAGAAAACACA[C/T]CTCCTGGCTTTTTAA | 55819 |
| rs575921320 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033574 | GTGCGCCTATAATCC[C/T]AGCTGCTCGGGAGTC | 55819 |
| rs576002248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179995950 | GCCTCTAATCTGCTG[C/T]CTTTGGGGGAAAAAC | 55819 |
| rs576005103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:179936644 | GTTAGCCTTTCATTG[C/T]TACTTTAAAGTAAAG | 55819 |
| rs576034098 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180044504 | AGTACCAAAGAGAGA[A/T]ACAATGTGGCAAACG | 55819 |
| rs576041447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016142 | GCAGAACGAAAGCCC[A/G]CCACCAACTTGCAAA | 55819 |
| rs576063345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180066885 | AAAAAATTAGCCAGG[C/T]ATAATGGCATGCACC | 55819 |
| rs576079663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016888 | CTTAAATACTTCCAC[A/G]GTCCCTCCTAAGAAC | 55819 |
| rs576087062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180031824 | TGTTTAAATAAATTG[C/T]CAAACTATTTTCCAA | 55819 |
| rs576098710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059779 | CAGACAGTGTGAAGA[C/G]AAAGCTGTAATGGTG | 55819 |
| rs576124667 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002564 | ACTCAGCTGGGCTTA[A/G]TGCCTGTGAGGACTG | 55819 |
| rs576148218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180024009 | TGCATGCTAATGGTA[C/T]TTTACAAATCCCTGT | 55819 |
| rs576152744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180060167 | GCAGTCTTGCCAACA[C/G]CTTGGTCTCACTGAG | 55819 |
| rs576157302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179963694 | TTGGCCCAAGGAAGT[A/G]AAGCAGGAGGTTTGC | 55819 |
| rs576179896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179963178 | ACACTCTAAGACTAT[A/G]CTGCTCCTTTGCCAC | 55819 |
| rs576186392 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179956758 | CAGAAGGGCCTTTGC[A/G]TACTCCCTCACTCTC | 55819 |
| rs576193695 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180009903 | TACATCCAAACCATG[C/G]GATATAGTTCGGCCA | 55819 |
| rs576227311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179922456 | TAGCTGAGATTACAG[A/G]CGTGGGCCACAATGC | 55819 |
| rs576267097 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007472 | ACTGGTTTTCCTTTG[C/T]TAATATTATGGCTTC | 55819 |
| rs576270723 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180018187 | GTAATCCCAGCTACT[A/C]GGGAGGCTGAGGCAG | 55819 |
| rs576282923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180019110 | CACTTTGAGGCCGGG[C/T]GGGGTGGCTCACGCC | 55819 |
| rs576312982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179923648 | TTCACCCATCCAGCT[A/G]GTTCTGTACCTCACT | 55819 |
| rs576349121 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF130 | GRCh38.p7 | 5:179988225 | TTTCCAGTATGTTAG[C/T]GTATAATTCTTCACA | 55819 |
| rs576357033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179986303 | AAATGGCAGCACCTG[A/C]AGCTGAAGACCTCTA | 55819 |
| rs576362724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041125 | AGGCCAAAATAATCC[G/T]CGGTTCAGTTACTAA | 55819 |
| rs576388197 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180032735 | GCCTTGATTACTAAA[A/G]TTGTGAAACGGAGTG | 55819 |
| rs576400507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179999182 | GTGTATCACCATGCC[A/G]GGCTGATTTTTGTAT | 55819 |
| rs576401941 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:180050624 | TCCTTCTGTGTTCCA[A/T]TTCCCTCCTCCTTAT | 55819 |
| rs576456711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179980929 | GAACTGGGACAGCTG[C/T]GTTAATGGTGTATAC | 55819 |
| rs576470447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179938650 | TAAGCTTAACATTAT[A/G]TATTTAAATAATTGT | 55819 |
| rs576498808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179981338 | ATCCAGGCCTTACAC[C/T]GTGGGAAAAGGCAGA | 55819 |
| rs576515501 | in-del | -/TTCT | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:180039156 | ACACATTTTATTTTA[-/TTCT]TTGTGTTTTTCTTTA | 55819 |
| rs576546094 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179944701 | CCAGAGTTTGAGGCT[G/T]CAGTGAACCATGATC | 55819 |
| rs576564425 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933573 | GTTGCCCAGGCTGGA[C/G]TGCAGTGGTGCAATC | 55819 |
| rs576582901 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF130 | GRCh38.p7 | 5:180067916 | GATTCATTAAAGGAA[C/G]CATTAAAGGCTTCGT | 55819 |
| rs576592064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975226 | AGGAATTCTGTAAGC[A/G]GCAGTTTGGTGAGCG | 55819 |
| rs576612639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180029325 | AAGTATTTCAATAAT[A/G]TTTTTCTAAGGTGAT | 55819 |
| rs576650066 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180060852 | AGGTGGGCGGATCAC[A/G]AGGTCGGGCGATCGA | 55819 |
| rs576657335 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179959304 | ATTAAATTTTCAGAC[A/C]CTTTTATGCTGAGTG | 55819 |
| rs576666643 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930317 | CGCCTTGGCCTCCCA[A/G]AGTGCTAGGATTACA | 55819 |
| rs576685343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180022291 | TCCATCCTCATGAAA[C/T]CTTCAGTTTACTTTT | 55819 |
| rs576703337 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964511 | ATACAATAAAATTAC[C/G]TATATATGTGCAAGA | 55819 |
| rs576728249 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179920407 | AGGGGACAAGGAGTT[G/T]CGATGAAAGAAGTGA | 55819 |
| rs576730755 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053590 | CAGTAATGATAGGAA[C/G]AAGCAAAGCTACTTC | 55819 |
| rs576754168 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937307 | AATCACGTATCTGAT[A/G]AGGGCCTAGTATCTG | 55819 |
| rs576767348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180035634 | GATTGAAATGTCTGT[G/T]TCTCCTTCCCATTCT | 55819 |
| rs576785226 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980693 | GAAGAGAAGGAATGC[A/G]TCACAGCTCCACTTC | 55819 |
| rs576824678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:180058595 | GAGTCTTGCTGTGTC[A/G]CCCAAGCTGGAGTGT | 55819 |
| rs576841903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180036217 | TTTAGTAACAGGCTG[C/G]GTTAAACACATGAAA | 55819 |
| rs576842296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179983997 | CAAATAATCTTCCTA[C/T]CTCAGCCTCACAAGT | 55819 |
| rs576851887 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051331 | CTCGGCTCACTGCAA[C/G]CTCTGCCTCCCGGGT | 55819 |
| rs576857733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180059052 | CCTCTTATATAAAGT[A/C]CAAAATCCTAACAAG | 55819 |
| rs576865906 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:179920950 | CACTGTGGAAGATGA[G/T]GATTTTCTCCTAACC | 55819 |
| rs576875146 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028760 | ATATAGCAGGTATAA[A/G]TCGATACCTGTTGAT | 55819 |
| rs576889006 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955133 | GGGTGCAGGGGCACA[C/G]TGGGGAGCAAATGTT | 55819 |
| rs576902257 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941775 | TAGTTCTTCTTGATA[C/T]GATGGTTGCACCACA | 55819 |
| rs576917449 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024065 | CCTAGCCTAATTATA[A/G]GAAAACTATCAAACA | 55819 |
| rs576929506 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021695 | AAAACTTTTAAAACC[C/T]AGAACCATTCAAGAG | 55819 |
| rs576952527 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179946745 | ATTTTTAGTAGAGAC[A/G]GGGCTTCACCGTGTT | 55819 |
| rs576986825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179947113 | ACCTGGGTTTCTAGA[A/G]TCTTCTCATCACTGA | 55819 |
| rs576987471 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983541 | TCCTGATTTCTGAGG[C/T]TTTGTAATAGATCTG | 55819 |
| rs576993930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179933827 | AAGAATCCCAGGATT[C/T]TCCCTCCTGTGTGTT | 55819 |
| rs577000846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179948214 | TCATTCAGATATTGC[A/G]AAGATTAAAATGGTT | 55819 |
| rs577037147 | snp | C/G/T | 0.0023933 | 0.0345097 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071766 | CGCCTAGAGGCGGGG[C/G/T]GGGCGCGGCCCGGGC | 55819 |
| rs577067045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179977585 | AGGCCGGGTGCGGTG[A/G]CTCACGCCTGTAATC | 55819 |
| rs577090295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180014476 | TTGGGAAAGAGAAAA[G/T]TATAACCACTTATTT | 55819 |
| rs577094030 | snp | C/T | 3.30196e-05 | 0.00406309 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179967008 | AGTACATGGCAAATT[C/T]GGCTGCAAAATATTT | 55819 |
| rs577114121 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:179942626 | AGAACAGAATTCTAT[-/A]CAGCAAAGCCATTTA | 55819 |
| rs577160870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179967695 | TTCTCTCAGCAGGCA[C/G]CAGCAGGCAGCACAT | 55819 |
| rs577167282 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072638 | TCATCAGGCGTTAGA[G/T]TCTCGTAAGAAGTGG | 55819 |
| rs577203149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180007347 | CAGAGGTTGCAGTGA[C/G]CCAAGATCGCGCCAC | 55819 |
| rs577203334 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004587 | CTCATCTGGTCAAAG[C/G]TGCAACAATAAACAC | 55819 |
| rs577203470 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033170 | ATTTTTTTGTAGAGA[C/T]AGGGTCCCCCTATGT | 55819 |
| rs577210582 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF130 | GRCh38.p7 | 5:180060835 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 55819 |
| rs577247910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF130 | GRCh38.p7 | 5:180061055 | CAGCCTGGGCGACAG[C/T]GAGACTCCGTCTCAA | 55819 |
| rs577304438 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF130 | GRCh38.p7 | 5:180014753 | CACTTTGGGAAGCCA[A/G]GGCAGGTGGATTGCT | 55819 |
| rs577326094 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010211 | GAGATCCAGCCGCTG[C/T]ACTCCAGCCTCGGCG | 55819 |
| rs577336623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180056223 | GTTACTCTTAGCCTA[A/G]GTGTTGAGCCTTAAG | 55819 |
| rs577374837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180038299 | GGCTCAAGCAATCCT[C/T]CTACCTTGGCTTCCC | 55819 |
| rs577415347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180000268 | TTTCTCTGGAAAAAT[C/T]TGTTTTTAGTCTAAT | 55819 |
| rs577418223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179943164 | CGCGCCACTGCACTC[C/T]AGCCTGGGACAGAGC | 55819 |
| rs577446485 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046772 | CCTAAGACTGAGTTG[C/G]GTGCTTTTTTCAAGT | 55819 |
| rs577463385 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979887 | CTCCTGGCTTTTTAA[C/T]GCACAAATGGTCCCA | 55819 |
| rs577487097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179993582 | GGTTGTTTGATTTTT[C/T]TCTTGCAAATTTGTT | 55819 |
| rs577506655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179979203 | TGGTCACCACTCCTC[A/T]GCCATTGAAATGCAA | 55819 |
| rs577507603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179987160 | CCTTTCCTTCCTTCC[C/T]TTCTTTCTTCTATTT | 55819 |
| rs577520326 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928517 | TCTTTGTTTCTTTTG[C/T]TCATTTTCCCATCAG | 55819 |
| rs577524483 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955823 | ATTAAGTGTTTTCCC[A/T]AAATCAGCAGTTTCA | 55819 |
| rs577525937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179969977 | GCTTGGGCAACAAGA[A/G]CAAAACTCCCTCTCA | 55819 |
| rs577548489 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992258 | GCCATTCTCCTGCCT[C/G]AGCCTCCCGAGTAGC | 55819 |
| rs577556906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179982105 | ACTTTTTGCTGTAAC[A/G]GTCTGCAACATCATG | 55819 |
| rs577568989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179975296 | TTGAAGAGCCGCGCA[A/C]AGCCATCCTCAGCTC | 55819 |
| rs577579697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180031179 | AGGCTTTTGGTCAAC[A/T]GCAAGCTATTAGTAA | 55819 |
| rs577588096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964477 | TACACACTGACTAGG[A/G]CTGTTTTAACAAAAT | 55819 |
| rs577608372 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179923526 | TGACAGACTGTAACC[A/G/T]ATTCTTGTACCAAGG | 55819 |
| rs577672359 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037731 | AGTGAAATTAATGAT[A/C]GCAGTGTGCAGATTC | 55819 |
| rs577676135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179996291 | ACACAGAACTGATTT[A/C]TGTATGTTAATTTTG | 55819 |
| rs577702454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179964779 | TCTCTGCCCACCTTA[C/G]CTTGTGTTATTAAAA | 55819 |
| rs577717437 | in-del | -/CTTGCATCAGGTGTA | 0.00159617 | 0.0282053 | intron-variant | RNF130 | GRCh38.p7 | 5:179956137 | GTGTGTGTTTCTGTC[-/CTTGCATCAGGTGTA]AAAACAGCCTATGAC | 55819 |
| rs577743212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179971456 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA | 55819 |
| rs577745626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180010352 | ATATGATTCCACCTA[C/T]ATAACATTTTTTTCT | 55819 |
| rs577757385 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045368 | TCCGGAGTTTCTTCT[C/T]ACTGGTGGGTTCGTG | 55819 |
| rs577768867 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:180041901 | GGGCGACAAAGTGAA[A/T]CAAAAAATACAAAAA | 55819 |
| rs577833762 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | RNF130 | GRCh38.p7 | 5:179945926 | AGGCGGGGGCAGGGA[C/T]ATTTAAATGGGGGCG | 55819 |
| rs577854394 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180004886 | CCCAATGCAAAGTGC[A/C/T]TTGTAGTCTGCACCC | 55819 |
| rs577863197 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970660 | GGGAATTTATTAAAA[C/T]ATAACTTGCAGAAAA | 55819 |
| rs577882318 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920774 | TCTCATCTGGGCATA[C/T]ATATTTATATATATA | 55819 |
| rs577884142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF130 | GRCh38.p7 | 5:179996750 | AAAATTTATGTTCAT[C/T]AAGGATACTTGTCTA | 55819 |
| rs577975940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034162 | GCACCTACCGAAAAT[A/G]GTTAGTTGGCTTTTT | 55819 |
| rs577979535 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072753 | CGGAGCTCAGGCGGT[G/T]ATGCTCACTCACCTC | 55819 |
| rs578011636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180069221 | AAGATCCCAGCAGAA[A/G]CTATGCTTCATAGAG | 55819 |
| rs578016225 | in-del | -/TTTTA | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179989795 | TTTGTAAATTCTTTG[-/TTTTA]TTTTTTCTTCTGTCT | 55819 |
| rs578031059 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | RNF130 | GRCh38.p7 | 5:179962618 | ATGTCCAAAATTTAG[-/AA]AACAAAACAAAACAA | 55819 |
| rs578050199 | in-del | -/A | 0.00120289 | 0.0244948 | intron-variant | RNF130 | GRCh38.p7 | 5:180025640 | TTATGAATTTTTTTT[-/A]AAAAAAATGTATGAA | 55819 |
| rs578051495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180012074 | GTTTGGGTGTTTTAT[A/G]TCTACTTTCAGATGA | 55819 |
| rs578059038 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180026979 | GGGCTCTGAAGACTG[C/G]AGGAGCCTTGGACTG | 55819 |
| rs578059092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180034746 | CATTACCTAATAAGA[C/G]TGACTCACTGTGAGT | 55819 |
| rs578062793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180020795 | ACACAGAGGCAGAAG[A/G]GGGGTGGGCACTGAA | 55819 |
| rs578072013 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960493 | CGAGCGTGGTGAGGA[A/T]GGGATGGGGGCTTGC | 55819 |
| rs578088399 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035004 | AGTTCCAAAGAACCA[A/G]CTTTTGGGTTTCGTT | 55819 |
| rs578089324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179930992 | GAGCTGAGATTGCAC[C/G]ACTGCTCTCCAGCCT | 55819 |
| rs578092885 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949981 | CCAGAGTGGAACACT[G/T]ACCCCATTTGTTTGA | 55819 |
| rs578103836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179965650 | ACCATAAAACCTCAA[C/T]GCCAAAGTAAGAAAA | 55819 |
| rs578120872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180062993 | GAAAGAATATCAGAA[C/T]GGTTTCAGAAGGTGA | 55819 |
| rs578151851 | snp | C/T | 0.000171057 | 0.00924658 | intron-variant | RNF130 | GRCh38.p7 | 5:180013030 | GAACTCTGGCTGTTA[C/T]GAACCAATCACTGTT | 55819 |
| rs578213133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057308 | AATCCCAGCACTTTG[G/T]GAGGCCGAGGCGGGA | 55819 |
| rs578219135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:179959746 | CTACTACTACACTAA[A/G]AGGAGGAAGATCACC | 55819 |
| rs578224754 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953096 | TTGTAGACAGAAAAG[C/T]CCAAGGAATCCACAA | 55819 |
| rs578226112 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992438 | TGAGCCACCACGCCC[A/G]GCCCTAAATCATTGT | 55819 |
| rs578228794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057281 | GGGGTGGGCACAGTG[A/G]CTCACGCCTGTAATC | 55819 |
| rs578233097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF130 | GRCh38.p7 | 5:180057520 | ACCACTGCGCTCCAG[C/G]CTGGGTGACAGAGCG | 55819 |
| rs578234824 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | RNF130 | GRCh38.p7 | 5:179925861 | GCCAAGTTGGAAGAC[A/G/T]TAGGCCCAGAACACA | 55819 |
| rs745337516 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991223 | GGTGCTTTTCTCTTG[A/T]TGATTTTAGAATTTT | 55819 |
| rs745359121 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973960 | CAAACCCAGCAATCA[G/T]GAAATTCAGCGCCCT | 55819 |
| rs745376454 | snp | C/T | 4.94287e-05 | 0.00497111 | missense | RNF130 | GRCh38.p7 | 5:180013123 | AGAATATGAGCCATG[C/T]TGAAGAAATAATCAT | 55819 |
| rs745378041 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928027 | TATAGCAACAGTTCC[C/T]TCCTTTTCACCGCCG | 55819 |
| rs745381208 | snp | C/T | 0.000186202 | 0.0096471 | missense | RNF130 | GRCh38.p7 | 5:179920426 | TGAAAGAAGTGACCA[C/T]CTGGAAAAGGAAGAA | 55819 |
| rs745389035 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056750 | GCTCATGACTGGACT[A/G]CATTGTTCTTAACCA | 55819 |
| rs745396963 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068639 | ATTCAGAAATTCACA[C/T]GTGCCAAACTGATAG | 55819 |
| rs745410134 | snp | C/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072541 | ACCATTTTGGCACTG[C/G]GGGACGGGTTTCCAG | 55819 |
| rs745461903 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070507 | CAAGCAAATCATGAC[C/T]TTATTTAGGTTGCCT | 55819 |
| rs745535311 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000722 | ATTGAATTCTTCAGC[G/T]GCAGGATTTGATTCT | 55819 |
| rs745537024 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957284 | AGGGGTGCTGGCAGG[C/T]GCCTCTAGTCCCAGC | 55819 |
| rs745566459 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045447 | ACAGCTCATAAAGAC[C/T]GCAGGGACCCAAACA | 55819 |
| rs745593740 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037585 | CATCAGTGTCACCTA[C/G]AAACTTGTTAATAAT | 55819 |
| rs745601562 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921674 | TGGTGGCATGTGCTT[A/G]TAGTCCCAGCTACTT | 55819 |
| rs745617055 | in-del | -/ACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954421 | GTTCTGACACATGCT[-/ACA]ACATGTATGAACCGT | 55819 |
| rs745625481 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955270 | CTGACCATCCTAAGC[A/G]GCATCACCAGCAGGA | 55819 |
| rs745644319 | snp | A/G | 3.79485e-05 | 0.00435578 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071553 | GCGAAACGTGAGCGG[A/G]GCGCCGCGGCCGGGC | 55819 |
| rs745665354 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995475 | ATCCTGGCATGAGAC[-/T]TTATAATGCTAACAG | 55819 |
| rs745678874 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033421 | CGTTCATAGCTAGCA[C/T]ATAGAAATACAATGG | 55819 |
| rs745691652 | snp | A/C | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920150 | CTACTGTCCTCAAAG[A/C]CTCACCTTGGGGGAA | 55819 |
| rs745702760 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935100 | CTGCGATTTCTTCTT[C/T]GATTCATGACTTTTT | 55819 |
| rs745714909 | snp | C/T | 5.31995e-05 | 0.00515722 | intron-variant | RNF130 | GRCh38.p7 | 5:179970528 | AATAATGGAGAATTA[C/T]GTCACAAGTTACATA | 55819 |
| rs745732811 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981058 | GGCCTGGACTAAGAC[C/T]GGGAAGGGGTTAGAT | 55819 |
| rs745733387 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926242 | TATAGGCCTAGGATT[-/TA]TTATTCATGTGCCCG | 55819 |
| rs745733804 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057891 | AGATGTGTGGGTACC[C/T]TTTGTCCCACTACCT | 55819 |
| rs745737712 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991482 | CTGAAACACCAATGA[C/T]TCAGTTTAGTTGCTT | 55819 |
| rs745748192 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956484 | CAGCAAGCAACTTCG[C/G]AGCCACTAGGAATAT | 55819 |
| rs745757744 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010360 | CCACCTATATAACAT[A/T]TTTTTCTTTATTTTT | 55819 |
| rs745773183 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026041 | GCTAGATAATAAATA[C/T]AGAGCTAAATACGTT | 55819 |
| rs745851110 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998892 | ATATATATGTTTTAT[A/C]TATCTGAGTGCTCCA | 55819 |
| rs745903348 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932506 | CTCAAATGATCCGCC[C/T]GCCTCAGCCTTCCAA | 55819 |
| rs745911027 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070430 | GAAGAAAACAGCTTA[C/G]CACTTTGGCATACAA | 55819 |
| rs745979253 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924426 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCGGTGAG | 55819 |
| rs745989850 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970928 | AGTGATTAGTTTTTT[A/G]GCACCCTGATTGAAT | 55819 |
| rs746009652 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996801 | TATCCTCATGTGGTA[C/T]TGCTATTAGGGTAAT | 55819 |
| rs746018925 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958871 | TTTTTAGTAGAGATG[G/T]GGCTTCACCGTGTTG | 55819 |
| rs746021924 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040126 | AGGCAATCCTTGAGA[A/T]TCCATGACATAACCT | 55819 |
| rs746067988 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014214 | TAATTTCCAGAAGTA[A/G]TAACAGTGAAGGAAT | 55819 |
| rs746098304 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | RNF130 | GRCh38.p7 | 5:179978218 | TTGCAGGGGAGAATT[C/T]GGACGACATCATTCT | 55819 |
| rs746099176 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997910 | ACAGTGGTGTGATCT[C/T]GGCTCACTGCAACCT | 55819 |
| rs746103840 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983960 | TGTTATGTTGCCCAG[C/G]CTGGACTCAAACTCC | 55819 |
| rs746152972 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059010 | ATCTTAAAACACCAA[C/G]AAAAATCCCTCCAAT | 55819 |
| rs746160192 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020406 | GTGGACGTGCTGTAC[A/G]CCACCACCACAGGAT | 55819 |
| rs746181562 | in-del | -/GAAAGGAGTAGGGAAAGGAGTAGGGAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015619 | TAGGGAAAGGAGTAG[lengthTooLong]GGAAAGGAGTAGGGA | 55819 |
| rs746195700 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063841 | TTTGTGTTTACAAAA[G/T]ACTTCTGTAAATACA | 55819 |
| rs746221032 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062956 | CACACACTGTAAAGA[A/C]GACATAGAAGCCCTG | 55819 |
| rs746229302 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950921 | TGCTTTGATCTCCAC[G/T]GAGATGAAACCAGGT | 55819 |
| rs746280900 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966918 | GGAGTTGTCGCCGGC[A/G]AGGTCGCCGAGGGCT | 55819 |
| rs746305200 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976637 | AAACTAGAATGACTG[A/G]ACTTCCAGAATCTTG | 55819 |
| rs746305318 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989700 | CTGTATCTTTTAAGC[A/G]GAGCATTTGATCCAT | 55819 |
| rs746318210 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969417 | AACATAAGCAATGAC[A/G]TCGTTTTATATTATG | 55819 |
| rs746319194 | snp | A/G | 3.69269e-05 | 0.00429676 | intron-variant | RNF130 | GRCh38.p7 | 5:180013328 | TGCAATATAAAATAA[A/G]TATATAACTCAAGTG | 55819 |
| rs746349247 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007395 | GACAGAGTGAGACCC[A/C]GTCTCAAAAAACAAA | 55819 |
| rs746366897 | snp | C/G | | | missense | RNF130 | GRCh38.p7 | 5:180040603 | GTTTGATATTAGGAG[C/G]GACAAAGAACCGGGT | 55819 |
| rs746386513 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055911 | CAACAGGGTGAAACC[-/CT]GTCTCTACTAAAAAT | 55819 |
| rs746397326 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977679 | CAACATGATGAAACC[C/T]CGTCTCTACTAAAAA | 55819 |
| rs746399768 | snp | G/T | 3.32265e-05 | 0.0040758 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015333 | GGCTATAAAGTAACT[G/T]AGACGGATCCCACAA | 55819 |
| rs746416212 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021144 | CTCATTTTTTTGTAT[A/T]TTTAGTAGAGACGGG | 55819 |
| rs746430205 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923381 | TTTCTGGGCACTATT[C/G]TGTTCTAGCAATCCA | 55819 |
| rs746432540 | in-del | -/TCTAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948360 | CTGTTTCACCGGGAC[-/TCTAT]TCTTTGTTCTGTTTG | 55819 |
| rs746452932 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023988 | CATAAACTTGGTATG[A/C]CAGGATGCATGCTAA | 55819 |
| rs746463383 | snp | A/G | 1.97658e-05 | 0.00314364 | intron-variant | RNF130 | GRCh38.p7 | 5:179963576 | TCTTCTGTTGACAAA[A/G]GAAAGGGAGGAAATC | 55819 |
| rs746465417 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024684 | TGATTTAAAAAAAGG[C/G]AAATGACACCAAACG | 55819 |
| rs746466869 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067462 | TGTAGATAACGTTTA[A/G]AGGTTCGCTGTAAGA | 55819 |
| rs746509983 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972215 | AATGCTGGCTACTGA[C/T]CAACAAAGACCACAA | 55819 |
| rs746521925 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066536 | AAGTTTGTTTAAAAA[G/T]ATTTGTCTTAGCCTG | 55819 |
| rs746529971 | snp | A/C | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955149 | TGGGGAGCAAATGTT[A/C]CAAGTCCCTGCTGCT | 55819 |
| rs746590662 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | RNF130 | GRCh38.p7 | 5:179980099 | CTGCTGGATTACTTT[C/T]ACGGTGCTGAAGTTG | 55819 |
| rs746623867 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044413 | TAATGAGACTTATTT[A/G]CCTCTTGACAGGCAC | 55819 |
| rs746627244 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973441 | GTTCTGCTACAACAG[G/T]CTGGTGCTCGGCAAA | 55819 |
| rs746634907 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961601 | CCCAATAATTCTCGA[A/C]AAGTGCCTAGTGTAA | 55819 |
| rs746636022 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970973 | CATTTTTAAAAACTT[A/C]TAAGCAACTTATGTT | 55819 |
| rs746666668 | snp | C/T | 3.32768e-05 | 0.00407888 | intron-variant | RNF130 | GRCh38.p7 | 5:179955714 | AAATTAAAGAGTAGT[C/T]AAATGTTTAAAATAA | 55819 |
| rs746677053 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056483 | GTAATTACTTAGATA[C/T]GGGAGTGGGGGGTCT | 55819 |
| rs746689679 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009962 | AACAACTTGAAAGTA[C/T]CTTGGCCGGGCGCAG | 55819 |
| rs746700478 | snp | A/G | 0.000118254 | 0.00768851 | missense | RNF130 | GRCh38.p7 | 5:180013299 | ATCATGACAGCAATA[A/G]TATCTCCAGTGCCTG | 55819 |
| rs746724785 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927952 | TTCTTTTGTGTCTAG[A/G]CTCTGTCTGACACAC | 55819 |
| rs746749246 | in-del | -/ATTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930044 | TTTTTTGAAAATTTC[-/ATTTT]ATTTATTTATCTTTT | 55819 |
| rs746757183 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014346 | TCAATCTATCAGCGA[C/T]TGTCCTTTCATAAGC | 55819 |
| rs746770318 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047106 | ACTAATTAGTTACCC[C/T]GGATTTAGATTCCTC | 55819 |
| rs746775675 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966055 | TGAAAGGAACATGTA[A/G]AGAATGGAAGCGAAG | 55819 |
| rs746806458 | snp | C/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072985 | TTAAAAGATACACAT[C/T]GCTATAAAGTATCAG | 55819 |
| rs746813120 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931528 | AATCCCAGCACTTTG[A/G]GGGGCCGAGGTGGGC | 55819 |
| rs746831643 | in-del | -/AAAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939222 | CTCTGTCTCAAAAAT[-/AAAT]AAATAAATAAATAAA | 55819 |
| rs746855583 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924355 | ACAAAATTAGCCAGA[C/T]ATGGTGGCGCATGGC | 55819 |
| rs746869014 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991249 | ATTTTTTCCTTCACA[A/C]TGACTTTAAGCAATC | 55819 |
| rs746878313 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002668 | CCTCACCACAGTGAG[C/G]TCTTCCTGGTTCCCA | 55819 |
| rs746886157 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974869 | CGGCATGGACCGCAG[A/C]AGACGGCCTCTCCGG | 55819 |
| rs746893046 | in-del | -/CTC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933134 | AGGACTTGGGAAGTT[-/CTC]CTCTTTTTCTAGTCT | 55819 |
| rs746902203 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954287 | TGTTCAGGCCAAAAT[C/T]TGTACATGAATGTTC | 55819 |
| rs746913943 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023124 | TTTAGTGATAAGAAA[C/G]GAGAGAGAGCTACAA | 55819 |
| rs746920251 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003617 | TGCGACAGGTAAACC[C/T]GTGACAGGTATAAGT | 55819 |
| rs746922877 | snp | C/T | 3.54516e-05 | 0.00421005 | missense | RNF130 | GRCh38.p7 | 5:180071558 | ACGTGAGCGGGGCGC[C/T]GCGGCCGGGCTCCTG | 55819 |
| rs746936308 | snp | C/T | 3.63405e-05 | 0.0042625 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071649 | CCACAGGCTGCAGGT[C/T]AGCAGGGCGAGCGCG | 55819 |
| rs746950453 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990661 | GCTACCGCTAGACCA[C/T]GGTCCGCTTGGTAAT | 55819 |
| rs746958420 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037372 | AGCAGTTGTGCTCCA[C/T]CGTAGGCATCCATGG | 55819 |
| rs746964886 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036473 | CCACACTGGCAGAAA[C/T]TCCACACAGCATAGC | 55819 |
| rs746980371 | in-del | -/AGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008236 | AGCCAAAGTACCAAG[-/AGA]AGGATGGCCTAACAT | 55819 |
| rs747024407 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021159 | TTTTAGTAGAGACGG[A/G]GATTCACCATGTTGG | 55819 |
| rs747038067 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061135 | ACAAGCTGCTAGAAA[A/G]AGTAAAGACTGTGGG | 55819 |
| rs747043173 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051995 | ATCCACATCACTCTT[C/T]GTTCCACAAAGGAAT | 55819 |
| rs747062004 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969070 | TGGGTTGCAAGCTAA[A/G]ATGAGTTCATCTGTT | 55819 |
| rs747062067 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956781 | TCACTCTCCAGCCAC[A/G]TCAGTACGCACATGA | 55819 |
| rs747071398 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063664 | TTGTCTTATTTCATT[A/G]CAAGAAAATATTTTT | 55819 |
| rs747074323 | snp | A/C | 1.66966e-05 | 0.00288929 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015343 | TAACTGAGACGGATC[A/C]CACAAACGACATATG | 55819 |
| rs747090340 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937415 | ATTCTCCAAAGAAGA[C/T]GTATGAGTGGCTAAC | 55819 |
| rs747094528 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050569 | AGTCAAGGTGAAACA[C/T]AGAATTCACCATCAC | 55819 |
| rs747095890 | snp | A/T | 1.65015e-05 | 0.00287237 | missense | RNF130 | GRCh38.p7 | 5:179966872 | GAGGAAGAGGTGAGA[A/T]CCCCGAAGTTCGAAG | 55819 |
| rs747114314 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005900 | CCAAGGATATAGAAA[C/T]GAATTATCTTGCAAA | 55819 |
| rs747118399 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977557 | TAGTGAGAACCCCAT[C/G]TTTAAAGAAAACAGG | 55819 |
| rs747119650 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922063 | AAAAAGATGGCCCTA[C/T]CGGCAGCCTATGGTA | 55819 |
| rs747129327 | snp | A/C | 1.68255e-05 | 0.00290043 | intron-variant | RNF130 | GRCh38.p7 | 5:180040436 | AAACAAAATCAACAA[A/C]CCTCATTTTTGTTTA | 55819 |
| rs747186098 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958679 | CAATTTTAACTACTA[C/T]AAAGTTGTTTCTTTC | 55819 |
| rs747199854 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995427 | CATTTCTGGCTGTGT[A/G]GGCCCCTTTCCTACC | 55819 |
| rs747203764 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996571 | TCTACTGGCATTACC[A/G]CATGGTTTTTGTTCT | 55819 |
| rs747212013 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180017023 | TAGCTGTTTAACTTG[-/T]TTTAGTTTTGTGTCC | 55819 |
| rs747220859 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936153 | TTGAGACAGGGTCTC[A/G]CTCTGTCACCCAGGC | 55819 |
| rs747266175 | in-del | -/TTCTG/TTCTGTG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055438 | TGAATGTCAGATGAC[-/TTCTG/TTCTGTG]TTTGTGTGTGTGTGC | 55819 |
| rs747280222 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039789 | GTGAAACTAACAGAA[C/T]ATCAACAAAACTAGG | 55819 |
| rs747285053 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069222 | AGATCCCAGCAGAAG[A/C]TATGCTTCATAGAGA | 55819 |
| rs747310571 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043954 | TAATACTGTAGTATA[A/C]TCATTCTACCTAGTT | 55819 |
| rs747330908 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949772 | TGCGTCGCTTGGCAC[A/G]CAGCTGCAACTTCTG | 55819 |
| rs747335044 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005110 | CGCACCAGAAAAGAA[C/T]TGTATATCACTCCAC | 55819 |
| rs747344442 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946296 | ATAGCCGCGCGGGGT[C/G]TGTGTGTGGTCAGGA | 55819 |
| rs747349282 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962712 | TGGATCAAAATGGAC[A/C/T]ATAACAGTCATCTAG | 55819 |
| rs747354071 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066226 | ATACTATTCTCGTGA[C/T]AGTGAATAAGTCTCA | 55819 |
| rs747357589 | in-del | -/AAGCTGGAAAAG | 0.000418961 | 0.0144674 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015438 | CCCTCTTGAAGACTC[-/AAGCTGGAAAAG]GAGTAGGGAAAGGAG | 55819 |
| rs747361379 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063711 | TTAAGTGCCCATTTG[A/G]TTTTTCTTAACATGT | 55819 |
| rs747361482 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073590 | ACTATTGATGACTTG[A/G]CAGACATCCTTTACA | 55819 |
| rs747375735 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987655 | CTATATTGAAGTATG[A/T]TACTTCTATACCTAA | 55819 |
| rs747379171 | in-del | -/ATTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925508 | TTCTTCTGTTTTTTC[-/ATTT]ATTTATTTATTTATT | 55819 |
| rs747441816 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000386 | GGAGGATGTTTTCAG[A/G]TTTACTCTTATTTAG | 55819 |
| rs747470468 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935884 | CAATGCAAGCATGTT[A/G]GAGCAGTTTTACCTC | 55819 |
| rs747485868 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922849 | AGAGGTGGGAGGATC[A/G]CTTGAGTCCGGGAAG | 55819 |
| rs747487184 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976458 | GTGGATGACGCCTCC[C/G]TGTGTCCCGCTGGCC | 55819 |
| rs747499754 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950693 | TAACAAAAATTCTCT[A/G]TCTGGCCTTGAACAG | 55819 |
| rs747532910 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033177 | TGTAGAGACAGGGTC[C/T]CCCTATGTTGCCCAG | 55819 |
| rs747599072 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021890 | CCTTTACAGCAGCCC[A/G]GGTCCGAGTCACATG | 55819 |
| rs747613875 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003597 | TTTAACATTTCCCAT[C/T]ACTTTGCGACAGGTA | 55819 |
| rs747618096 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062677 | TACCTGAACCATTTT[A/T]TTCCAGATGAAAAAG | 55819 |
| rs747627055 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952779 | ACAAAGCTTCCGACA[C/G]AATCAAAAACTATTT | 55819 |
| rs747630488 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036203 | CTTGTTCACTTTTGT[C/T]TAGTAACAGGCTGGG | 55819 |
| rs747667176 | in-del | -/GAACC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028563 | TCCAGACCTGGGTCA[-/GAACC]CCTTTCGTAATAACA | 55819 |
| rs747669112 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065406 | TGTGTAACACTCCAC[A/T]GAGTGGATATATCAT | 55819 |
| rs747672441 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017485 | CAATGCTCTCAGCAT[-/C]CACTGGTGTTTGCCT | 55819 |
| rs747691196 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954025 | AGTCACTAGGGTAAT[A/G]CATGTTAAAAACATG | 55819 |
| rs747739088 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949538 | GACAAAACAACCTGT[C/T]TCTTGCATTACAAAA | 55819 |
| rs747772584 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008989 | AAAGAAAAAAATACA[C/T]AGGACTGAATGAAAA | 55819 |
| rs747829577 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022909 | ATTAAGTAGAGAGTT[A/C]GGCATTCTAACCAAG | 55819 |
| rs747833953 | snp | C/T | 1.65946e-05 | 0.00288046 | missense | RNF130 | GRCh38.p7 | 5:179966851 | TCGGAGTGAGCTCCC[C/T]ATCCTGAGGAAGAGG | 55819 |
| rs747837096 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028744 | TCACAGAATGCCTGG[A/C]ATATAGCAGGTATAA | 55819 |
| rs747840009 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973084 | AAGTTCCTTTGGGCT[C/T]TCCATCCACCCCATC | 55819 |
| rs747858959 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978825 | CTCAATTCAATACTC[A/G]GTCTTCATTAAGAGT | 55819 |
| rs747889745 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058750 | TATTTTTAGTGGAGA[C/T]GGGGTTTCACCATGT | 55819 |
| rs747901262 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994438 | TTCATCCCTTGTAAG[C/T]TGGATTCCTATGTAT | 55819 |
| rs747937556 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070344 | GGACTTTTCAAAGCC[G/T]AGTCTGAGTTGCGGA | 55819 |
| rs747957325 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052655 | AATGACAGGCCAGGA[C/G]CCATGCAGCTCACAC | 55819 |
| rs747978968 | in-del | -/CG | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072921 | CCACCTTCCGAAACG[-/CG]CGCGCGCGCGCACAC | 55819 |
| rs747979659 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016550 | CTTCCACGTCTGGCC[A/G]CCAGTACTAACTGTC | 55819 |
| rs748024460 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983847 | ACTACATAGGGCATA[C/T]TGCATATTTTGTCAG | 55819 |
| rs748025693 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035239 | TTTCATTTTCGTTTG[A/G]TTCCAAATGTTTTTA | 55819 |
| rs748032933 | snp | C/G | 0.000748643 | 0.0193329 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920293 | CAAAAGCAGTGACCC[C/G]AACAGCCAGGCCATG | 55819 |
| rs748060372 | snp | C/T | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:179980133 | CATGACTGTACCTTG[C/T]CACCCTTCTTTACTG | 55819 |
| rs748064655 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014142 | GCACAGGCTATGCAA[C/G]TTAATTACGAGGACA | 55819 |
| rs748068124 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931905 | ACCTGTGAACTTCCC[A/G]CCATATCCCAGATCT | 55819 |
| rs748078951 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960482 | GGTCAATGCACCGAG[C/T]GTGGTGAGGAAGGGA | 55819 |
| rs748100646 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046740 | AAAATGTCTTCTCCA[G/T]AACGCTTTCCCAGCC | 55819 |
| rs748117154 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001815 | TCCACTCTCCAAGAG[A/G]AAGGTTATCTAAGCA | 55819 |
| rs748156826 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059314 | GAGTCTCTTCTGCCA[C/T]TTATGCTCTCAGCAT | 55819 |
| rs748187621 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062377 | CCCAGCCTCTTTTAT[A/G]AGGGCACTAATCCCA | 55819 |
| rs748225572 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | RNF130 | GRCh38.p7 | 5:179966950 | ATCTTCGGTTAACAG[C/G]TTGGGTTCTGGTGAG | 55819 |
| rs748236810 | in-del | -/TGT | 1.65993e-05 | 0.00288086 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015274 | AGAAATCTCTTAAAA[-/TGT]TGTTCAACGGGCCAT | 55819 |
| rs748245043 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949630 | TAAATAGTAAACAAA[A/T]ATTATTCAACTTTAT | 55819 |
| rs748261756 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934447 | TTCCTGATAATGGTC[A/C]TTTGGGTCTTCTTTC | 55819 |
| rs748261829 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999080 | CAGGCTGGAGTGCAG[C/T]GGTGTGATCTCAACT | 55819 |
| rs748308602 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995749 | AACACTGACTCCCCA[-/T]TCTCCTGTATTGGGG | 55819 |
| rs748326646 | in-del | -/AAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989554 | TGTTTTATCTGGCAT[-/AAG]AATAGCTATTCTTAC | 55819 |
| rs748339675 | in-del | -/AAAAAAAAAAAAAAAAAAAAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055260 | TCTCAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAAAC]AAAAAAAAACAGCAA | 55819 |
| rs748349025 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004718 | GCCAAATGGTTCAGA[A/G]TATATTGAGGATAGG | 55819 |
| rs748358832 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921968 | GGAGGTTGCAGTGAG[C/T]GGAGATTGCACCACC | 55819 |
| rs748382455 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005707 | AAGGTCACAACCTAC[A/C]TTCTCTGTGAAGTGT | 55819 |
| rs748387071 | snp | A/T | 1.64838e-05 | 0.00287083 | missense | RNF130 | GRCh38.p7 | 5:180040487 | TGGCTCCTCTTTGGA[A/T]TTATTATTGTAGATG | 55819 |
| rs748390575 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038604 | CTTACTGTTTCCCCA[C/T]GAGTCCTCTAGGAAC | 55819 |
| rs748408686 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939498 | GCAGCAGCTGCTCCT[C/T]ATGCTGGCCGTCTTC | 55819 |
| rs748431454 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968227 | ATGAACCCAGGAGGC[A/G]GAGCTTGCGGTGAGC | 55819 |
| rs748433375 | in-del | -/A | 1.65488e-05 | 0.00287647 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955622 | TTTTTCCTTCAAGGC[-/A]AAAATCAGTCAGAAA | 55819 |
| rs748439926 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050372 | CTGACTCCAGGGAGT[A/G]TCACTTTTTTGTTCT | 55819 |
| rs748464065 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021679 | TTCGAAATATCATAT[A/G]AAAACTTTTAAAACC | 55819 |
| rs748470773 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043100 | AGGTGGGAAGACCAC[C/T]CAAGGCCAGGAGTTC | 55819 |
| rs748475400 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054955 | ATATAGAACTACAAC[A/T]GACTTAATTTTTGTT | 55819 |
| rs748504250 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013133 | CCATGCTGAAGAAAT[A/G]ATCATCAAAACAATA | 55819 |
| rs748520336 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998153 | CTGTTTTTGCTTTTA[C/T]AGTTCCTTGAGATGC | 55819 |
| rs748584146 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009766 | TTTATCCCAGGGAAA[C/T]GAAAACTCATGTTTA | 55819 |
| rs748596344 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987750 | TGTTCCTTTATTCTG[C/T]TGATGTGAAACATCA | 55819 |
| rs748617327 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962577 | TGAATATTGGTAAAA[C/G]AAAGGACTGAACGAT | 55819 |
| rs748652979 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031762 | TTTCATTTCTCTTAG[A/C]TATCTGGGAGTGGGA | 55819 |
| rs748684882 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016438 | CTGTAACGCTGTAAA[C/T]ATCAAAGCACATTTG | 55819 |
| rs748703996 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031082 | ATTTTCTCTTCCTTA[C/T]GATTTCCTTAATAAC | 55819 |
| rs748707583 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925473 | ATAACAGGCATTGGA[A/G]CTAGAGAAGCATGGC | 55819 |
| rs748761247 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951056 | ACATGCTCGGCTGAA[C/T]TCTGGCATTGTGAGT | 55819 |
| rs748766337 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046126 | TGCGCGGTGGACCGC[A/G]GCGCGTGCAGGCCCA | 55819 |
| rs748793312 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011119 | ACCTGAAACTAATCA[C/T]GAAGGAACACAACAC | 55819 |
| rs748793739 | snp | A/T | 1.64741e-05 | 0.00286998 | missense | RNF130 | GRCh38.p7 | 5:179980152 | CCTTCTTTACTGTCC[A/T]GGTTGTCAATTTACT | 55819 |
| rs748803680 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965201 | CCATCATAAAACACC[C/G]AATATGCTGGCAGCA | 55819 |
| rs748804513 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964053 | GCCGTCTGCGAGCCG[A/G]CCTCCCATGGCATCC | 55819 |
| rs748809010 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032979 | CTCCATTTATCCAGA[-/T]TTTTTTTTTTTTTGA | 55819 |
| rs748845297 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990417 | TTGCTATCTAGAGGG[C/T]GGAGCCAGGTGTACA | 55819 |
| rs748878957 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029112 | CTTGTGACTGTTTGA[-/C]ATTTATGCCAAATTC | 55819 |
| rs748890566 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021536 | TAACAATTCTTAAAA[C/T]GTGCAAAGACAGCCT | 55819 |
| rs748894063 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952599 | TGCAAAAATCCTCAG[C/G]AAAATACTAACAAAC | 55819 |
| rs748935885 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954009 | GATGCTTTGCATCTT[C/T]AGTCACTAGGGTAAT | 55819 |
| rs748941365 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943284 | TGTGGGAGGGATTTT[G/T]TTGGGGAATGTGTGT | 55819 |
| rs748967977 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039664 | TTGCTAAAAATAATT[A/C]TGTAAAAATTACACG | 55819 |
| rs748989287 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951937 | TTTATAGCTATAAAC[-/A]AACTACATTAAATAA | 55819 |
| rs748990653 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068813 | TTTCATGAATTTCAC[G/T]TATTGGCCACAGCTG | 55819 |
| rs749045626 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973271 | TTCTCTTCACCCATG[A/G]CCCTCCTCTCCTGTC | 55819 |
| rs749069307 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940234 | ACTTTCTTTTTTTTC[-/T]TTTTTTTTTTTTGAG | 55819 |
| rs749078595 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031419 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAAC | 55819 |
| rs749101143 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943559 | AAGGGGATAAAGAGG[A/C]AAAGGCGTAACATGT | 55819 |
| rs749123712 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956706 | GCAGCCTTTTCAGCT[A/C]CCCCAAAGGTAAGGC | 55819 |
| rs749133280 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981320 | AGACGTCACTCTAGA[A/C]ACATCCAGGCCTTAC | 55819 |
| rs749149938 | snp | A/G | 1.65299e-05 | 0.00287483 | missense | RNF130 | GRCh38.p7 | 5:180040615 | GAGGGACAAAGAACC[A/G]GGTTTGTGGATCACA | 55819 |
| rs749163781 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995324 | AAACCACACCTCTCA[A/G]GCAAATCTCCTGCTC | 55819 |
| rs749207080 | snp | C/T | 0.000371333 | 0.0136209 | missense | RNF130 | GRCh38.p7 | 5:179920361 | AAGAAGGTTCGATGG[C/T]GGAGAATTCACTTTC | 55819 |
| rs749259356 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982167 | TACTACTGTGTGTAC[A/G]GCTTCTTTGACTCAG | 55819 |
| rs749280695 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981646 | CACCTCTAATAGACA[C/T]GGGCTTTTGTTAGAT | 55819 |
| rs749282970 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060105 | AGGCAGCTTCTACAA[A/G]CTGAAAAAGGCAAGG | 55819 |
| rs749283409 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019534 | TCCCAAGACTTCTCA[A/T]CTCACTCCACTGACT | 55819 |
| rs749323680 | snp | G/T | 1.75099e-05 | 0.00295883 | intron-variant | RNF130 | GRCh38.p7 | 5:179970518 | ATGCCTATAAAATAA[G/T]GGAGAATTATGTCAC | 55819 |
| rs749327979 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948213 | CTCATTCAGATATTG[C/T]GAAGATTAAAATGGT | 55819 |
| rs749384476 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072363 | GTGTGAGAACAGACT[A/G]CAAAGGAAAAAAAGC | 55819 |
| rs749392011 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979930 | GAAAATGCATGCTAG[C/G]TTTTAGCAGAAGAAA | 55819 |
| rs749393202 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061292 | ACCACAACAACTGAC[A/G]TGACTTCAGGCACAT | 55819 |
| rs749396624 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961239 | GTGCATACACAACAT[G/T]CACGCACACACACAC | 55819 |
| rs749404321 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966188 | TTCTTTCCTGCTAGT[C/T]GACAGTGCAATGTGA | 55819 |
| rs749459404 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975315 | CATCCTCAGCTCAGC[A/G]GTTCTCATCTGGAGG | 55819 |
| rs749484134 | snp | A/C/T | 0.000152803 | 0.00873967 | missense | RNF130 | GRCh38.p7 | 5:180071539 | CGCCCGCGGTCGATG[A/C/T]GAAACGTGAGCGGGG | 55819 |
| rs749492713 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018002 | CTGGGTAATTGAGAA[A/G]GAAGAGGTTCAGGCT | 55819 |
| rs749500485 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997953 | TCAAGCAATTCTCCT[-/G]GCCTCAGCCTCCCGA | 55819 |
| rs749547155 | snp | C/T | 3.29489e-05 | 0.00405874 | intron-variant | RNF130 | GRCh38.p7 | 5:179970377 | ACATATAATAATATA[C/T]AAAAGTGGTAACAAA | 55819 |
| rs749598967 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924720 | CTTAAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 55819 |
| rs749608547 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022829 | CTCTTTCAAGTAAGA[C/T]GCTTACATTTATGCT | 55819 |
| rs749614697 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053464 | AGCAAGAACACACAA[A/G]ACAAATTAAGCTTTA | 55819 |
| rs749629772 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049668 | TTAACACTATTCTGA[A/G]AAGCAGCCCACAGGT | 55819 |
| rs749636528 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940080 | GTGTCATTCTCCAAC[A/G]TGCTGTTTTAATATC | 55819 |
| rs749647193 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971039 | TTTTAAGGGGTAAAC[A/T]GTGCCTAGATTCAAG | 55819 |
| rs749653031 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938885 | AAAGCCGATTCATGC[C/T]GGCGTTAGGGTACAA | 55819 |
| rs749665790 | snp | A/T | 1.79864e-05 | 0.00299881 | intron-variant | RNF130 | GRCh38.p7 | 5:180013316 | ATCTCCAGTGCCTGC[A/T]ATATAAAATAAATAT | 55819 |
| rs749669321 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065315 | ACCATTTTTATGTCT[A/G]CATCCTATCTGGAGT | 55819 |
| rs749745713 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043008 | TCACAGAATTTTACA[C/T]GTGAAAAAGCCAAGA | 55819 |
| rs749770147 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971976 | TAGTCTTAAATTCAC[A/G]GACAATGAAATAACC | 55819 |
| rs749797461 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029507 | CCAAGAATCTTTTCA[C/T]ACACTAAGATGAGTA | 55819 |
| rs749827231 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013163 | AAAGGATATTGACAC[A/G]AAGACTAGAGAGCCA | 55819 |
| rs749836498 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008807 | GAGAATCACTTGAAC[C/G]CGGGAGGTGGAGGTT | 55819 |
| rs749843894 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989661 | CACACAGTTGTGTCA[C/T]TTAAAAAAATCTATT | 55819 |
| rs749850739 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041927 | AAAAAAATTAGCTGG[A/G]TGTGGTGGGGCACAT | 55819 |
| rs749865271 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070110 | CCACGTGACCCTCAC[A/G]GTTCTCTCCACCAGA | 55819 |
| rs749877440 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027147 | GCACAGGAGCAGGAC[A/G]GGGTGAAAGCACGGG | 55819 |
| rs749879545 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925288 | CGCCCATGGCCAACA[-/G]GTTTAATCAGTCATG | 55819 |
| rs749958259 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958205 | TTTAGACAAGTGTTT[C/T]TCAAAACTAAAGCAT | 55819 |
| rs750075675 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012854 | CTGACTAGAATATTC[C/T]AGGTGATCACAATAA | 55819 |
| rs750097179 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046046 | GGCGTGGACGGAGGG[C/G]GGTGGGGCTCGGGCA | 55819 |
| rs750108893 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028053 | TTACCCTATCCACCA[C/T]GTTGAGCTGTGCTGT | 55819 |
| rs750142396 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070906 | GTGACATTTTCAGGC[A/G]TCAAATTACAGTAAA | 55819 |
| rs750150103 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058390 | TCAACAGTATTTTAA[A/C]ACATGCTACAACACA | 55819 |
| rs750150525 | in-del | -/ACG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062116 | CTGGAGTGCAGTGGC[-/ACG]ACCTTGGCTCACTGC | 55819 |
| rs750164110 | snp | C/G | 1.82244e-05 | 0.00301859 | missense | RNF130 | GRCh38.p7 | 5:179966822 | TGTTACTGCAATGTT[C/G]ATTTCTCCTGTTCTC | 55819 |
| rs750188609 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977134 | CTGGAACCTGCTATC[A/G]GCTCACCATCCTTCA | 55819 |
| rs750191247 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063178 | GAACCTTTAAGATTA[G/T]TTTGGCTACTATAGA | 55819 |
| rs750198057 | in-del | -/T | 1.71202e-05 | 0.00292572 | intron-variant | RNF130 | GRCh38.p7 | 5:180013020 | GATGACTGTGAACTC[-/T]TGGCTGTTACGAACC | 55819 |
| rs750218665 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950355 | TCCCTGGGCTCAACT[G/T]ATCCACTTGCCTCAG | 55819 |
| rs750241137 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976333 | AATGGTTTTGGAGGC[A/C]CGTAGTTTTAGGTGC | 55819 |
| rs750278987 | snp | C/T | 2.73041e-05 | 0.00369477 | missense | RNF130 | GRCh38.p7 | 5:180071630 | CGTTGTCTGCCCGTG[C/T]CGGCCACAGGCTGCA | 55819 |
| rs750301436 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019787 | GCTGTCACTCTGCTT[C/T]CAAAAGCCTTTGATG | 55819 |
| rs750325099 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025425 | ACCCACTTGGGACAC[A/G]GAGACTGCAAGGAAG | 55819 |
| rs750328445 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968812 | GACATTTCTGACTGT[C/T]GTGGCTGTGGTGCCA | 55819 |
| rs750328514 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995095 | TTGCCAAACCCTGTA[C/G]AAATGCCTAGGCAAA | 55819 |
| rs750337598 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923746 | CTTTGAACCTATTTC[C/G]GTCCTGGGGGCTGCC | 55819 |
| rs750338175 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007044 | TTACTATGCTTAGAA[A/G]GTTATTTACAATATA | 55819 |
| rs750386006 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002888 | CTAAGGATTTCTAAT[C/G]GGTCATTTTCCTAAG | 55819 |
| rs750386887 | snp | C/T | 3.44193e-05 | 0.00414831 | intron-variant, missense | RNF130 | GRCh38.p7 | 5:179963529 | AGAGTGTGAGGGCAC[C/T]GAGGAGGCCAAAACT | 55819 |
| rs750408133 | snp | C/T | 0.000116093 | 0.00761794 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015284 | TAAAATGTTGTTCAA[C/T]GGGCCATGATCTGTG | 55819 |
| rs750451199 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054679 | TCTTAATTTTATTAT[G/T]TGTTTTCAAGATTGT | 55819 |
| rs750456972 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941318 | TGCCTCTGGAAGTGA[C/T]GTATCACTTTTAGAA | 55819 |
| rs750458499 | snp | C/T | 1.64784e-05 | 0.00287035 | intron-variant | RNF130 | GRCh38.p7 | 5:179980095 | AAAACTGCTGGATTA[C/T]TTTTACGGTGCTGAA | 55819 |
| rs750469884 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045177 | AGATCTCATTTGCAA[C/T]GAGAGAAGGAGAAGA | 55819 |
| rs750475159 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986656 | CTGTTAATTTTATGC[A/G]GTTATGATTTAACAT | 55819 |
| rs750484836 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971691 | AAGAAATTTTTAAGT[A/G]AGATGCCAAATTGAA | 55819 |
| rs750499567 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980426 | GGTCAAACAGAAATA[C/T]AGAACTATAGGTCTT | 55819 |
| rs750503207 | in-del | -/AG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951124 | GGAATCTCAATGGAT[-/AG]AGGTGTATGAATAAC | 55819 |
| rs750504181 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939822 | AAGAAGTTGAATGAA[A/C]ATGGGTCCCTCCCAC | 55819 |
| rs750561295 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972514 | CAGGAATGGGAGGCA[C/T]CCCGCTGGGGGTCGG | 55819 |
| rs750570353 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926506 | CAAAAAAAATTAGCC[A/G]GGTGTGGTGGCGCAT | 55819 |
| rs750576633 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023443 | CATTACTGATAAAGT[A/T]CAATAATGCTCAAGG | 55819 |
| rs750580042 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043952 | CTTAATACTGTAGTA[C/T]ACTCATTCTACCTAG | 55819 |
| rs750594867 | in-del | -/CCA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025208 | CTTGAGATCCTAACT[-/CCA]AGGTCAGGTCCATCA | 55819 |
| rs750640668 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030786 | ATATAAATGGAATCA[C/T]ATAATAGTAGCCTTT | 55819 |
| rs750682540 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042729 | ACCCTGGAAGAAAAC[A/G]CAAAATCAAGAATAT | 55819 |
| rs750693660 | snp | A/C | 0.0105204 | 0.0717601 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071691 | AGGGCCCGCCCGCCC[A/C]GCGCAGCTCATCGTC | 55819 |
| rs750735401 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980274 | TATTTTTAAGCAATT[A/T]AAAGTATAAAGTCTC | 55819 |
| rs750738692 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927057 | AGTTTGCTTTTTCTA[A/G]TCACCGTCAGAAGTG | 55819 |
| rs750757934 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030506 | AAATTCACTCACGCC[A/G]TTTTTAAAAATACAT | 55819 |
| rs750759408 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046468 | TAGAAATGTAAACAC[A/G]CCACATAAGAAGCAC | 55819 |
| rs750798583 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974667 | AGTGGGCAGGTGTGA[C/T]AGCAGACGCTGTGGG | 55819 |
| rs750844185 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | RNF130 | GRCh38.p7 | 5:180040534 | TGTGGAAAGCGGCCC[A/G]TGATATTTTCTCTTT | 55819 |
| rs750870652 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002165 | CCTGGGAGGCGTGGC[A/G]CTGCTTCAACTGAGA | 55819 |
| rs750871183 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022711 | CTTAAGCCACGTCTC[C/T]ACAAACCTTTGCTAT | 55819 |
| rs750876636 | in-del | -/AGGG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063462 | GCAGTGGTAGCAGAT[-/AGGG]AGGTGAAAAAATGAA | 55819 |
| rs750903972 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934018 | TGAAGCTCACAACAG[C/T]GTTCCCAGCTCTGTG | 55819 |
| rs750921158 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066156 | CCCATAATTTCCACA[C/T]GCTGTGGGAGGGACC | 55819 |
| rs750922685 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990976 | TTGGAATAGCTCGTG[A/C]CCTCGGTCTCTTGCC | 55819 |
| rs750923979 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995927 | AGTGGGTTAGGCATG[C/T]TGGAAAAGCCTCTAA | 55819 |
| rs750930522 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993887 | GTCTTTAATCCATCT[C/T]GAATTAATTTTTGTA | 55819 |
| rs750937726 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953791 | TTAAAACTTTGTGCT[C/T]TGAAAGACACTACCA | 55819 |
| rs750967896 | snp | C/G | 1.65693e-05 | 0.00287826 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015292 | TGTTCAACGGGCCAT[C/G]ATCTGTGGTATAAGA | 55819 |
| rs750968443 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064960 | AACTGCTCAAAATTA[C/T]GACATATTTTAGCTT | 55819 |
| rs750983128 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990348 | TACGTCATCATTTCT[C/T]CTATGCTCTTTTCAG | 55819 |
| rs751054733 | in-del | -/T | 1.86268e-05 | 0.00305173 | intron-variant | RNF130 | GRCh38.p7 | 5:179970552 | TACATACCAAGAAAC[-/T]TTATTAGGCCAAAAT | 55819 |
| rs751087460 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936571 | TAGATGTTTAGGTTG[A/G]CAGATATTTTTCCTC | 55819 |
| rs751090260 | snp | C/G | 1.66774e-05 | 0.00288763 | missense | RNF130 | GRCh38.p7 | 5:179966845 | CTGTTCTCGGAGTGA[C/G]CTCCCCATCCTGAGG | 55819 |
| rs751105960 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921466 | AGAACTGAAATTACT[A/G]CAAAAACTGAACTTT | 55819 |
| rs751116438 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992364 | GCCAGGATGAGTCTC[A/G]ATCTCCTGACCTCGT | 55819 |
| rs751127677 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967890 | TAGGCTCACACCCAG[A/T]TAAAAGAGGTTTTTT | 55819 |
| rs751169060 | in-del | -/GC/GTGC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055455 | TGTGTGTGTGTGCGT[-/GC/GTGC]GTGTGTGTGTGTGTG | 55819 |
| rs751200153 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026968 | AGGCACAGAGAGGGC[C/T]CTGAAGACTGCAGGA | 55819 |
| rs751200870 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025794 | AAATCCATATTCAAT[C/T]AGAAGCTAAAAAACT | 55819 |
| rs751221345 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943176 | CTCCAGCCTGGGACA[C/G]AGCGAGACACTGTCT | 55819 |
| rs751244133 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069820 | AGGACTAATCTTCAT[C/T]CATACCTCAATACAC | 55819 |
| rs751244808 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039557 | ACAAGTCAGAGGGCA[C/T]TAAAGTTGAAATCCA | 55819 |
| rs751285697 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960335 | AGATCTGTTTGCAGT[C/G]TTAAAAAAATTTAAT | 55819 |
| rs751286364 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975232 | TCTGTAAGCGGCAGT[C/T]TGGTGAGCGCGAAGG | 55819 |
| rs751299132 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068592 | AAAAAATTGACTATT[C/T]GCTCTTTAAAGGGAT | 55819 |
| rs751299732 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983471 | ATGTGGGTCTATGTG[C/G]GGACACTATTGTACC | 55819 |
| rs751303441 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016320 | CTTGACTTTTAAGGA[A/T]CTGAGGAGCTCTGGC | 55819 |
| rs751303465 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957403 | GGTGAGAGAGCGAGA[A/C]CCTGTCTCAAATAAA | 55819 |
| rs751314979 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962249 | TGTGAGCCTCAACAT[C/G]TATGGCTCACAGATG | 55819 |
| rs751318439 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060800 | CAGAAAGCTATGTTC[A/G]GCCGGGCGCCTGTAA | 55819 |
| rs751329353 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062503 | GGTGGGACACCAACA[C/T]TGAGACTACAGCACC | 55819 |
| rs751330923 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073861 | CTAAGACCCAGAAAT[G/T]CCTTCTCCCCACAGC | 55819 |
| rs751336748 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947285 | AAAATGCATGGGCCT[-/C]CTGACTGCTGCCCAC | 55819 |
| rs751338685 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949152 | TGTATTTTAGTAGAG[A/C]TGGGGTTTCGCCATG | 55819 |
| rs751345113 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988129 | CATTACTATTTATTG[C/T]TCTGTTCATGTTTTC | 55819 |
| rs751357118 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948078 | AGCATTGACTCTGGG[C/T]TGCCTGGGTCTCATT | 55819 |
| rs751367986 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071736 | CGCTGCTCGCGGACC[A/G]GGCTCCGGGGCCGGC | 55819 |
| rs751374339 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986740 | TTAACTTTTTACAAT[A/G]GATTTTTGTATATTT | 55819 |
| rs751424624 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026347 | AACAATAACAGTAAA[-/G]TCTATATAAATCTTT | 55819 |
| rs751458576 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031511 | AAGTTAAATTTGGGG[A/G]GAGGCAAAAGTTATA | 55819 |
| rs751470162 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976221 | GAAAAGTCAACACTG[A/G]AGGGATGAAGATAAT | 55819 |
| rs751541406 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948354 | TGGTCTCTGTTTCAC[C/T]GGGACTCTATTCTTT | 55819 |
| rs751542890 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950277 | ACCTGCCACCACGCC[C/T]GGCTAATTTTTGTAT | 55819 |
| rs751546493 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017808 | AGCTCCTTTGGGCTC[C/T]GGAATCGGAGGGTCT | 55819 |
| rs751579726 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032752 | TGTGAAACGGAGTGT[A/G]TAAGTCCTCTAATGC | 55819 |
| rs751593602 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952115 | AGGTAGGAGGATTGT[G/T]GGAGCCAGGGAGTTC | 55819 |
| rs751632950 | snp | C/T | 1.66757e-05 | 0.00288749 | missense | RNF130 | GRCh38.p7 | 5:180013069 | AGCTCACCTGGTTCC[C/T]GTCGCGTGCATTTGT | 55819 |
| rs751642230 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953548 | GTCTCTTAAACAAAT[A/G]GCACTGGGAAAACTG | 55819 |
| rs751658805 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965540 | GTAGTAGGTGCTCAA[C/T]AAATGTTTGATCAAT | 55819 |
| rs751665662 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067962 | TTTTAAACATGAAAA[-/C]CTAAGATTCACTTTT | 55819 |
| rs751677903 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938406 | GTCAGGGGCCGGGGG[G/T]ATTGCAGAATGGGGA | 55819 |
| rs751679400 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008428 | CCAGAGAACATGCCA[C/T]CCAACAGCAGAATAT | 55819 |
| rs751687798 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979352 | ATACGGTGGTATCAA[A/G]GCAATGGGAATAAAA | 55819 |
| rs751733306 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990331 | AGAGAGAGAGGACAG[C/T]TTACGTCATCATTTC | 55819 |
| rs751757696 | snp | A/C/T | 3.30875e-05 | 0.00406729 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955652 | AGCAGGTTTTTTCTT[A/C/T]TTCAAAACCATTCTA | 55819 |
| rs751762880 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970616 | TTCCCCCTTTCAGGA[C/T]ATATTTTAAGCCCCA | 55819 |
| rs751808204 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058210 | GCAAAGCTGGCCACA[A/C]TCAACTTCTCCACTA | 55819 |
| rs751808405 | snp | C/T | 1.65789e-05 | 0.0028791 | intron-variant | RNF130 | GRCh38.p7 | 5:179967039 | CCAGGTTAAAAATAA[C/T]TGTAAGGAAAACACA | 55819 |
| rs751811680 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007320 | GCAGGAGAATTGCTT[A/G]AGCCGAGGAGGCAGA | 55819 |
| rs751831320 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041496 | TCACTCTGCACATAT[A/G]GCCATCATGGTTCTG | 55819 |
| rs751858480 | snp | C/T | 0.0012945 | 0.0254081 | missense | RNF130 | GRCh38.p7 | 5:180071489 | GCGCCAGCACCTGGC[C/T]GCGGACCTCGGCCTT | 55819 |
| rs751860043 | in-del | -/TGTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928471 | CATACATTTGCAGGC[-/TGTT]TGTGTATCTGGTTCG | 55819 |
| rs751865376 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | RNF130 | GRCh38.p7 | 5:179980199 | GCATCTCCGAGACGA[C/T]GCTATGAAAATTGCA | 55819 |
| rs751873549 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939508 | CTCCTTATGCTGGCC[A/G]TCTTCTCCCATTTCT | 55819 |
| rs751882001 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052956 | AGGCAGGTCTCAAGA[C/T]TGGCCTATAATGATG | 55819 |
| rs751886951 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974310 | CCACTTCTGAAAACG[C/T]ACTTCTAACGACTAC | 55819 |
| rs751895935 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069470 | ACACAGAATGACCCC[G/T]AGGGAATCAAGGAAA | 55819 |
| rs751919953 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963655 | ATGCAACGAAGCAGA[C/T]GTCAACGGAGGTGTA | 55819 |
| rs751927995 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031983 | TTTTGGTTGCACTGT[C/T]GTTTTGATTGCATTT | 55819 |
| rs751962005 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964694 | TTAGATTTTAAAGGT[G/T]GTGACTTTCAAAAGG | 55819 |
| rs751975033 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973864 | GAAAAGCACAAGCAT[A/T]CTGAGCGCCAACAAA | 55819 |
| rs751975088 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982711 | CAGCCTCTGGAATAG[C/G]AGGAACTACAGGGGT | 55819 |
| rs752019265 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013764 | TGCTGTTTTTATAGC[A/G]TAAATTGGTACTTCT | 55819 |
| rs752021870 | snp | C/T | 3.35413e-05 | 0.00409506 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179970491 | GGGATCCACGCAGGA[C/T]TTGTGGAAAACATGC | 55819 |
| rs752026677 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034646 | GTAAACATAGCAGGT[A/T]TGAACTACTATCCGT | 55819 |
| rs752027813 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012626 | AGAGGTTTTTCATTG[A/G]TTTCATTTTCTGAAT | 55819 |
| rs752049493 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989508 | CTATTATCTATTTAC[A/G]TTTTTTAATTTTTAT | 55819 |
| rs752069890 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002140 | ACTCTGGATGGCCAA[A/T]GCACCACTTCCTGGG | 55819 |
| rs752085757 | snp | C/T | 1.64776e-05 | 0.00287028 | missense | RNF130 | GRCh38.p7 | 5:180040569 | GTGCAGTTTCCCCTC[C/T]GCAGCAAGGCAATCC | 55819 |
| rs752111234 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058534 | AGAGGGGGTAATGGA[C/G]TCTTGTCATTTAATG | 55819 |
| rs752123163 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001366 | AATGACAATGGGACC[A/G]TGTCCTAGGCTCAGA | 55819 |
| rs752158443 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022862 | TTACAAGCTTTTGAT[-/A]AAAAGAATTTTAAAT | 55819 |
| rs752186568 | snp | C/T | 1.64738e-05 | 0.00286995 | missense | RNF130 | GRCh38.p7 | 5:179966913 | CCAAGGGAGTTGTCG[C/T]CGGCGAGGTCGCCGA | 55819 |
| rs752233035 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948805 | TCTAAAGTGACAACC[C/T]AGCTAGCCAATGAGA | 55819 |
| rs752265213 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057365 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC | 55819 |
| rs752285559 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933943 | CTGCCATTTTTTCTA[G/T]ATCTTTGAGCTGCAC | 55819 |
| rs752319593 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037239 | GTCCATGCACATGTG[C/T]GAGAGTAACAAGGGT | 55819 |
| rs752342352 | snp | A/C | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954868 | CATTTACAAATACTG[A/C]AAATCCTTCAAGCAT | 55819 |
| rs752342454 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996388 | GAAAGTGGGCATCCT[A/G]TGTTTTTCCACATCT | 55819 |
| rs752347711 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967751 | TGTGAGAAGTTTGTA[C/T]GTTTATAGAGAGAAG | 55819 |
| rs752358791 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921237 | CGAACATATCCATTA[C/T]CCCAAAGTTTCCTGG | 55819 |
| rs752359270 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038122 | GCAGTGGTGTGATCA[C/T]GGCTCACTGTAGTCT | 55819 |
| rs752369931 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938348 | AATTCATATGAAGCA[C/G]CAGAACAGGTATATC | 55819 |
| rs752419354 | snp | C/T | 2.72135e-05 | 0.00368863 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015427 | CAGTTGAGGCTCCCT[C/T]TTGAAGACTCAAGCT | 55819 |
| rs752425177 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934579 | GGGGACAGGGTCTGA[-/CT]CTGTTGCCCAGGCTG | 55819 |
| rs752439559 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071330 | GACGGAAGCCTCGAC[C/T]CTGGCTGGGGCTGTC | 55819 |
| rs752444576 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971422 | TCGCCCAGGCTGAAG[G/T]GCAGTCGTGCAATCT | 55819 |
| rs752469729 | snp | A/G | 3.29495e-05 | 0.00405877 | intron-variant | RNF130 | GRCh38.p7 | 5:179980224 | ATTGCAAATAAAAAC[A/G]GATACTAAGTGTAAG | 55819 |
| rs752473041 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997619 | AGGTGTGAGCCACCG[C/T]GAGTGGCCTTATGTT | 55819 |
| rs752476594 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926872 | TTCCAGGTAGACAGC[A/G]TTGGAACTGAATTGA | 55819 |
| rs752493650 | snp | A/G | 1.65787e-05 | 0.00287907 | missense | RNF130 | GRCh38.p7 | 5:180013075 | CCTGGTTCCTGTCGC[A/G]TGCATTTGTGTACCT | 55819 |
| rs752500824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959843 | CATTTGCTCTAGTTA[C/T]TTCGTCACCTTTACC | 55819 |
| rs752520458 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999345 | TGATACAAGTACAGC[A/C]ACTCCTGCTTAGTTT | 55819 |
| rs752529820 | in-del | -/GAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028562 | TCCAGACCTGGGTCA[-/GAAC]GAACCCCTTTCGTAA | 55819 |
| rs752568942 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986302 | GAAATGGCAGCACCT[A/G]CAGCTGAAGACCTCT | 55819 |
| rs752643411 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986544 | GAACTACTCATAAGC[A/G]TATGTCACATGACAT | 55819 |
| rs752670231 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072933 | AACGCGCGCGCGCGC[A/G]CACACACACGACTCT | 55819 |
| rs752684203 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924269 | GGGAGGCTAAGGCGG[G/T]TGGATCACCTGAGGT | 55819 |
| rs752696698 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065684 | AGAATTGCTTGAACC[C/T]AGGAGACAGAGGTTG | 55819 |
| rs752725821 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006152 | CAGTTCTTCTGGAAT[A/T]GTTAATCCTTAAGAA | 55819 |
| rs752774088 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026070 | TTTTTAAGAGAATAT[G/T]ATGGAAAAAAGGTGA | 55819 |
| rs752793761 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990230 | GGCAGGGTAAAGAGT[C/T]TGAGTCACCTCCAGT | 55819 |
| rs752796988 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930118 | GCTAGAGTGCAATGG[C/T]GTGATCTTGGCTCAC | 55819 |
| rs752800850 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989451 | TGTTGGGTGTATAAA[C/T]ATTTTGAATTGTCAT | 55819 |
| rs752830394 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051809 | GTAAGTTTAAATGAC[A/G]GCTAATACAAATCAC | 55819 |
| rs752830396 | snp | C/G | | | intron-variant, missense | RNF130 | GRCh38.p7 | 5:179963496 | TCAAGCTAGCTGTGG[C/G]TCTGATGATCATGTA | 55819 |
| rs752837113 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020866 | GTGAAGAATTTCCAG[A/G]GGTTGCCAACTTTCA | 55819 |
| rs752860067 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001167 | ATGGGTGCCTCAGTG[C/G]TATAAGCTGTGGATG | 55819 |
| rs752894077 | snp | C/T | 1.65603e-05 | 0.00287747 | splice-acceptor-variant, intron-variant | RNF130 | GRCh38.p7 | 5:179955671 | AAAACCATTCTACCC[C/T]ATGGAATAAAAGGAA | 55819 |
| rs752894793 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069009 | AAATTGTTAAACTCA[-/T]TAAATCAAGATTATA | 55819 |
| rs752954731 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064678 | ACTATCTCTTGAATC[C/G]CCATCCTGTGAGATG | 55819 |
| rs752998697 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020163 | AGGCCCAGGGAGCAG[A/C]TATGGGACCAGGCTC | 55819 |
| rs753003163 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937321 | TAAGGGCCTAGTATC[C/T]GGAATGTATAAAGAA | 55819 |
| rs753026589 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049370 | ACATTTGGATGAGGG[A/G]AAATCATCTTTATTT | 55819 |
| rs753030444 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073436 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55819 |
| rs753036020 | in-del | -/AAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048480 | TGACTTAGATTGATT[-/AAAA]ATAATGAGGCCAGGT | 55819 |
| rs753085562 | snp | G/T | | | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180072039 | TCGCAAGGACGCGGC[G/T]GGGGAGGGGAAGGGC | 55819 |
| rs753096371 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000296 | AATAGGGATTCTCTT[A/C]TGTGACTTGATGCTG | 55819 |
| rs753098679 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973819 | GTGGTGCATCGGGAC[A/G]GAAAGCAGGTAACGT | 55819 |
| rs753105910 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994582 | TGTTCAGTAGCAAAT[A/G]TTCTAGGATTTCCTT | 55819 |
| rs753130544 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053825 | AAAAGCAAATACATT[-/C]TTTTTTTTTTTTTTT | 55819 |
| rs753166532 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980729 | CGCTATACTATCATC[A/C]TCTGGGATCCTGGGA | 55819 |
| rs753186401 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944096 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 55819 |
| rs753193796 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044901 | CACAGAAGCTGACGT[C/T]AGAGGGTGCCAACAC | 55819 |
| rs753202513 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013387 | GTATCAACACGCTAC[-/T]TAGGTAACTACTATA | 55819 |
| rs753225507 | snp | C/T | 1.66488e-05 | 0.00288515 | missense | RNF130 | GRCh38.p7 | 5:179970424 | CCACAATTCCCAGGG[C/T]CTTCAATATATTAAG | 55819 |
| rs753234906 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955393 | CACATTCTGTCTCTG[A/G]AACACAAACAAATGC | 55819 |
| rs753236451 | snp | C/T | 1.71056e-05 | 0.00292446 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179970506 | TTTGTGGAAAACATG[C/T]CTATAAAATAATGGA | 55819 |
| rs753244767 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929193 | TTATAAATATTCAGT[A/G]GAGCCAGCACCATCT | 55819 |
| rs753245780 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038211 | AGGAATGCACCATCA[C/T]ACCTGCTAATTTTTG | 55819 |
| rs753256103 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974714 | GATGGCTTTGAAAGA[A/G]AGTTTTAAAAACTGG | 55819 |
| rs753296935 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071111 | CCAAAATACAGGCTG[A/C]GACGTCCTCCCCATG | 55819 |
| rs753321394 | snp | C/G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960903 | ATAAAGGCAAAAACA[C/G/T]AAATAAAATAGATGT | 55819 |
| rs753334445 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956769 | TTGCGTACTCCCTCA[C/T]TCTCCAGCCACATCA | 55819 |
| rs753340799 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930937 | GTTCCAGCTACTGGG[A/G]AGGCTGAGGCATGAG | 55819 |
| rs753351841 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030379 | AACAGCCTTAATGAG[A/G]TATAATTTACATCCT | 55819 |
| rs753367772 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968667 | GAGACTCTGTCTCAT[-/A]AAAAAAAAAAAAAAA | 55819 |
| rs753386820 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965840 | TTGGTTAAAAACATG[A/C]ATACTTTGATTGAAC | 55819 |
| rs753412230 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060281 | GTGATTTGTTACTGC[A/G]GCAATAAGAAACTAA | 55819 |
| rs753457493 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984509 | CATCTATTGAGATCA[G/T]ACAGTTTTAGCTTTT | 55819 |
| rs753481510 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975103 | GTCCCGTGGGAAGAC[A/G]GTGAGGGAACAGAAC | 55819 |
| rs753537208 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035972 | CTTTGGACATATTTA[C/T]ATTAATTGCTTTGAA | 55819 |
| rs753537709 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022027 | GTTGATCTGTCGAAG[A/G]TATTTCCCTGTGGCT | 55819 |
| rs753558685 | snp | A/G | 3.29533e-05 | 0.00405901 | missense | RNF130 | GRCh38.p7 | 5:180013221 | GTTCCAACAGCTATT[A/G]TCATTTGTACAGAGA | 55819 |
| rs753573691 | snp | C/T | 1.65446e-05 | 0.00287612 | intron-variant | RNF130 | GRCh38.p7 | 5:179967021 | TTCGGCTGCAAAATA[C/T]TTCCAGGTTAAAAAT | 55819 |
| rs753592228 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046613 | GGCGGCCGCACAGCA[C/G]AGTGGCAAAGATGTG | 55819 |
| rs753600815 | snp | A/G/T | 8.28952e-05 | 0.00643751 | intron-variant | RNF130 | GRCh38.p7 | 5:179955684 | CCTATGGAATAAAAG[A/G/T]AAAAAAGAGGTCATA | 55819 |
| rs753607880 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938160 | ATGGGGTTTTGCCAC[A/G]TTGCCCAGGTTGGTC | 55819 |
| rs753610706 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059115 | GTGCCCCACTCTCCC[A/C]CTTACTCTCTAACTC | 55819 |
| rs753616715 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052726 | TAAGCTAAATTGGTG[A/G]GGAGGGAGGGAGGAA | 55819 |
| rs753630722 | snp | G/T | 1.6473e-05 | 0.00286988 | intron-variant | RNF130 | GRCh38.p7 | 5:179963460 | CAATCCAAAAACAAT[G/T]TGTTACTTACTCATT | 55819 |
| rs753632052 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021126 | ACGTACCACCAAACC[C/T]GGCTCATTTTTTTGT | 55819 |
| rs753640867 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007281 | TGACACACATCTTTA[C/G]TCCCAGCTACGTGTG | 55819 |
| rs753642763 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942764 | TCAAATATGTGATGT[G/T]TTCTTCAGAGATGCT | 55819 |
| rs753649489 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978059 | GCTGGCCTCAGCCCC[A/G]TGGCCAGCAATGCAC | 55819 |
| rs753651383 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968924 | GTCACTAATGCCCGA[A/T]ACTTTGAGAAATCCC | 55819 |
| rs753684515 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042432 | TTTAACCCTTCCTCA[A/G]TCAAATTAAACGGGG | 55819 |
| rs753689515 | in-del | -/CTGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972441 | GACGATGGGACTTGG[-/CTGA]CTGACAGGTAATGGA | 55819 |
| rs753779930 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028318 | TGTGTGTCTTGTTTA[G/T]GCTTGGAGCTCTAAC | 55819 |
| rs753787853 | in-del | -/TTTC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047172 | TGAATTAGATTATAA[-/TTTC]TTTATTCTTTAAATT | 55819 |
| rs753794683 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013100 | GTACCTGATCTTCTG[A/G]ATGAAGTAGAATATG | 55819 |
| rs753825881 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008295 | TCTACTCCAGCCAGG[C/T]GCCAAGGGCAAAATC | 55819 |
| rs753850140 | in-del | -/AA | 1.86946e-05 | 0.00305727 | intron-variant | RNF130 | GRCh38.p7 | 5:180013334 | ATAAAATAAATATAT[-/AA]CTCAAGTGACATTTA | 55819 |
| rs753855378 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988805 | TTTTGTGGTCTAATA[C/T]ATAGTGTTTCTAAAC | 55819 |
| rs753862739 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959496 | AGCTGGGCGTGGTGG[C/T]GGGTGCCTGTAATCC | 55819 |
| rs753876877 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070186 | CTCAACCACAGTGAC[G/T]GGCACAGAGCAGGAA | 55819 |
| rs753884664 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063104 | AGACTTCTGATGTCC[A/G]TTCTAAGGATGATGA | 55819 |
| rs753885394 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927493 | ACTACCAGCGCCCTA[A/C]AAGTCCCTCCAGTGA | 55819 |
| rs753887112 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929062 | AAGGTTTTGATGACA[C/T]TTTATCTTATTTTTT | 55819 |
| rs753888863 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044116 | ATTAAGTGAAGACAT[A/G]TTATGGTGTAAAATA | 55819 |
| rs753914004 | snp | A/G | 0.000335627 | 0.0129499 | missense | RNF130 | GRCh38.p7 | 5:180071677 | GCGGCGAGCCGGGCA[A/G]GGCCCGCCCGCCCCG | 55819 |
| rs753922299 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921137 | TATAACTGACATACA[A/G]TGAAAAGCACATGTT | 55819 |
| rs753935558 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943098 | TACTCAGGAGGCTGA[A/G]GTAGGAGAATTGCTT | 55819 |
| rs753946739 | snp | C/G | 2.39461e-05 | 0.00346012 | stop-gained | RNF130 | GRCh38.p7 | 5:180071601 | GATGAGCGCCGTGTA[C/G]TACTCCTGGCTCGCG | 55819 |
| rs753951800 | in-del | -/CTGAGATTGTGCCATTGCACT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924442 | GGAGGTTGCGGTGAG[-/CTGAGATTGTGCCATTGCACT]CCAGCCTGCGCAACA | 55819 |
| rs753977867 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032920 | TTAAGATAACTGCCA[A/C]CCTGACAATACTGAA | 55819 |
| rs753980770 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972918 | AAGTGCCCACCCCTC[C/T]GTTTTACTAAACAAT | 55819 |
| rs753986030 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948487 | CAAGCCTAGCCAACA[C/T]GGTGAAACCCCCATC | 55819 |
| rs753987129 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999519 | CTGAGGTCAGGATTT[C/T]GAGATCAGCCTGGCC | 55819 |
| rs753991894 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988253 | ACAAACCTCTAATGA[C/T]CCTTTGTATTTTGTT | 55819 |
| rs753996623 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant | RNF130 | GRCh38.p7 | 5:179978165 | GCATACAAAGCACAT[C/T]AATATCATTCTTTCT | 55819 |
| rs753996699 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062246 | TTTATTTTTTTAGTA[C/G]AGATGGGGTTTCACC | 55819 |
| rs754017014 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010842 | TCATGTGAATCTACA[C/G]ATGCGATAAAACTAC | 55819 |
| rs754057494 | snp | C/T | 0.000198717 | 0.0099659 | intron-variant | RNF130 | GRCh38.p7 | 5:179966803 | GCGGAGGCCCCCACT[C/T]ACTTGTTACTGCAAT | 55819 |
| rs754066173 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054110 | TGAGCCCCTGCGCCC[A/G]GCCAGCAAATACATT | 55819 |
| rs754091825 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971587 | TGTTAGCCAGGATGG[C/T]TTCCATCTCCTGACC | 55819 |
| rs754141699 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949563 | ACAAAAGTTTGTCCA[A/G]GAAGGGTTTAAAACT | 55819 |
| rs754144975 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970216 | TTCTCTTCCAGGAGT[-/TC]TCTGAGATGGATTAG | 55819 |
| rs754165225 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963240 | GTGGCTAATGAAAAC[C/T]TCTGGATCTTTTCTC | 55819 |
| rs754181935 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061272 | AGGATGGTCTTTTGG[-/A]AAAAACCACAACAAC | 55819 |
| rs754191378 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920940 | ACTGAATTCCCACTG[C/T]GGAAGATGAGGATTT | 55819 |
| rs754235346 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966609 | AGCTATTCCTATTAA[C/T]TATACACAAACACAC | 55819 |
| rs754260357 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980571 | CCTGCTGCTCCAATG[A/G]CTTTTGGATTCTGCT | 55819 |
| rs754270244 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991060 | TTCTCCTTCACTTAC[A/G]AAGTTTATTCTAGCT | 55819 |
| rs754278875 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009648 | ATGGTATGGCCACTT[C/T]GCAAAATGAGTCTAA | 55819 |
| rs754304207 | snp | C/G | 1.6569e-05 | 0.00287824 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015311 | TGTGGTATAAGATAC[C/G]AGGTATGGCTATAAA | 55819 |
| rs754332102 | snp | C/T | 6.82804e-05 | 0.00584256 | intron-variant | RNF130 | GRCh38.p7 | 5:179978336 | CTGCAAGTATATAAA[C/T]GGTTGGGATGCAATT | 55819 |
| rs754365369 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930618 | AACCTTATTTACAAT[C/T]TTAGGGAAAAAGTTT | 55819 |
| rs754373023 | in-del | -/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072281 | CGCTGGTGCTGGTTG[-/T]TTTCTCTGTCAGGCG | 55819 |
| rs754379521 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025358 | CTGCTGCCAGTGAGG[A/G]AAGAGAAGCACAGAA | 55819 |
| rs754381944 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941559 | TTGAGCTCTCCTTCT[C/G]TCTCGGTCTTTGGGC | 55819 |
| rs754416640 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959557 | TCTTGAACCCGGGAG[A/G]TGGAGGTTGTGGTGA | 55819 |
| rs754416676 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920797 | ATATATATATATATT[-/A]TTTTTTTTTGAGATG | 55819 |
| rs754440088 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065986 | TAAAATTATTCAATC[A/G]AAAAGGTAATATCAC | 55819 |
| rs754447376 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002363 | AGATGTGGGGCCACT[A/G]TGCTGGGGTGGTTTG | 55819 |
| rs754465020 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972557 | TGCCTTGACTTCTGA[G/T]CAGGGCTCTGGTGCA | 55819 |
| rs754500666 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014108 | AGCCTCTAACAGTTG[C/T]CCAGAGGTCTGCCCA | 55819 |
| rs754530377 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966723 | TGTTGCAGGCTGAGG[A/C]GAGTGCCTTGACTCT | 55819 |
| rs754537770 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059597 | ATGCAAATGAGAAGG[C/T]GCATCACTGACCTTT | 55819 |
| rs754555530 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996292 | CACAGAACTGATTTC[G/T]GTATGTTAATTTTGT | 55819 |
| rs754570570 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953947 | TAAAGCACCGGGATA[C/G]ACATTTCTCCAAAGA | 55819 |
| rs754581617 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991076 | AAGTTTATTCTAGCT[A/G]GATGAAAATTTTTCT | 55819 |
| rs754585772 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983875 | AGATTTATTGTTAAG[-/A]AATTTCCTATTTGTT | 55819 |
| rs754639235 | snp | C/T | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919808 | GGCCTTCTCTCAACC[C/T]CCTTTAGAAGGGGCC | 55819 |
| rs754672987 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003580 | GAGTTTTTAATCAGT[C/T]CTTTAACATTTCCCA | 55819 |
| rs754740520 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931577 | AGTTCGGGACCAGCC[C/T]GGCCAAAATAGTGAA | 55819 |
| rs754745283 | snp | G/T | 1.65674e-05 | 0.00287809 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015300 | GGGCCATGATCTGTG[G/T]TATAAGATACCAGGT | 55819 |
| rs754763138 | in-del | -/AAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065772 | TCAAAAAAAAAAAAA[-/AAC]CAACTATGTAAAGAA | 55819 |
| rs754782842 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027380 | CCAGTGTATAATGAC[C/T]TTCTCTGAGTATAAG | 55819 |
| rs754804222 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058552 | TTGTCATTTAATGGG[C/T]ATGTTTTTATTTTTT | 55819 |
| rs754826517 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039064 | AGCTAAATTAAACTG[C/T]CCCTTAATTTTCTTT | 55819 |
| rs754830038 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039714 | AATAAGCCAAACTCT[A/G]AAATTCTCATGAATG | 55819 |
| rs754832777 | snp | A/T | 3.29484e-05 | 0.00405871 | missense | RNF130 | GRCh38.p7 | 5:179966910 | AGGCCAAGGGAGTTG[A/T]CGCCGGCGAGGTCGC | 55819 |
| rs754838771 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071174 | GTCTACGCTGTCCCT[G/T]CAAACTCCTAGCTCA | 55819 |
| rs754844050 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958607 | TAGCTTCTGTCTGAA[A/G]AATCAGGTCCTGGTG | 55819 |
| rs754861048 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062798 | GCTGAAGCCTCAGAT[A/G]GGGGACTTGACTTGT | 55819 |
| rs754862358 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924170 | GGCAACACAGTGAGA[C/T]CCTGTCCCTAAACAA | 55819 |
| rs754869546 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974423 | AAAGGAGAATCAGCC[A/G]TGATCACTGAGCCGA | 55819 |
| rs754879873 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061157 | GACTGTGGGTGACGC[A/T]TCAGGATTCAGCAAG | 55819 |
| rs754933390 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959551 | ATAATTTCTTGAACC[C/T]GGGAGGTGGAGGTTG | 55819 |
| rs754940674 | in-del | -/T | 1.99328e-05 | 0.0031569 | intron-variant | RNF130 | GRCh38.p7 | 5:180013355 | AGTGACATTTAAAAC[-/T]TATGGAAACATCAAA | 55819 |
| rs754946553 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000160 | CCCATTTCTGAAGGA[C/T]GGCTTTGATGGACAC | 55819 |
| rs754963780 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944398 | ATAATTGACTTAACA[A/G]TTATGTACAGATCTA | 55819 |
| rs754979714 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983472 | TGTGGGTCTATGTGC[A/G]GACACTATTGTACCA | 55819 |
| rs754987574 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997484 | TCCCACCACCACACC[C/T]GGCTAATTTATTTAT | 55819 |
| rs755004099 | snp | C/T | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920099 | AATGATCAGCTTGGG[C/T]GGGTTTTCAATACCA | 55819 |
| rs755062413 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929151 | TTCAGTATAGTGTGA[A/C]GTAGGAATTAAGATT | 55819 |
| rs755071465 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989552 | CTGTTTTATCTGGCA[-/T]TAAGAATAGCTATTC | 55819 |
| rs755087176 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935181 | ATCTTTTTGTTATTG[A/C]TTTATAACTTAATTC | 55819 |
| rs755129357 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021166 | AGAGACGGGGATTCA[C/T]CATGTTGGCCAAAAT | 55819 |
| rs755151354 | in-del | -/TCAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990265 | ATAAGGTCACGTGAG[-/TCAC]TCACATGTCCACTGG | 55819 |
| rs755153327 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962539 | AGGACCCCAGGGTTG[C/T]TTTCATCTCTAATTA | 55819 |
| rs755181188 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949606 | ATTAAATTTTAATCT[C/T]GAATTTTTTAAATAG | 55819 |
| rs755222505 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018090 | ACCTGAGGTCAGGAG[C/T]TTGAGACCAGCCTAG | 55819 |
| rs755244789 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926691 | AATCTCAGAGTTGTG[C/T]GAGCTGCTGTAGCAA | 55819 |
| rs755249079 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979819 | TCTAGTGAAAAAATA[A/G]AACAACAAAAGAGAC | 55819 |
| rs755275386 | in-del | -/TTCCT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987156 | TCCTCCTTTCCTTCC[-/TTCCT]TTCTTTCTTCTATTT | 55819 |
| rs755316047 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953342 | TTGAGAAGTTGATTC[C/T]AAAATTCATGCAAGG | 55819 |
| rs755317582 | snp | C/G/T | 3.39993e-05 | 0.00412295 | missense | RNF130 | GRCh38.p7 | 5:179970502 | AGGATTTGTGGAAAA[C/G/T]ATGCCTATAAAATAA | 55819 |
| rs755330159 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054838 | GAAAAGTCTGTTTAT[G/T]TACATCTTTAATTCC | 55819 |
| rs755344970 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066359 | TGAGGCCTCCTCAGC[A/C]ATGTGAAACTGTATA | 55819 |
| rs755362228 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067190 | AAGCTTTGTCATCTG[A/T]CAGGTAGCTAAGCCT | 55819 |
| rs755399642 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940155 | CTGTGCTTAACAGAC[A/G]GTTGGAATGGGCAAG | 55819 |
| rs755400363 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022880 | AAGAATTTTAAATGG[G/T]TGGGAAAAGAAACAT | 55819 |
| rs755419783 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043044 | GCTTTCTGGCCAGGC[A/G]TGGTGGCACACACCT | 55819 |
| rs755422293 | snp | C/G | 1.64819e-05 | 0.00287066 | missense | RNF130 | GRCh38.p7 | 5:180040584 | TGCAGCAAGGCAATC[C/G]ACTGTTTGATATTAG | 55819 |
| rs755423606 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929296 | GCTGTTTCAGAACTC[-/T]TATTTTGTTCTGCTG | 55819 |
| rs755428756 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010900 | ACAAATAAGTACACA[C/T]TAAACTGGAGAGGTG | 55819 |
| rs755471556 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927510 | AGTCCCTCCAGTGAC[C/T]GCCCAATCACTATGT | 55819 |
| rs755499221 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999549 | CAACACGGTGAAACC[C/G]TGTCTCTACTAAAAA | 55819 |
| rs755525447 | in-del | -/AC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028719 | CTTCTACAAATCCCT[-/AC]AGTGTCCATCACAGA | 55819 |
| rs755548737 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971995 | AATGAAATAACCAGA[A/T]CCATCACCCCTGAAG | 55819 |
| rs755550389 | snp | C/T | 0.000323363 | 0.0127113 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071517 | CTTGGGGGAGTCAAG[C/T]CCGTAGCGCCCGCGG | 55819 |
| rs755573002 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012944 | CATATTAAAATGACT[A/G]AGTGAGGGTAACAAC | 55819 |
| rs755579862 | snp | A/T | 6.6346e-05 | 0.00575922 | intron-variant | RNF130 | GRCh38.p7 | 5:179967043 | GTTAAAAATAATTGT[A/T]AGGAAAACACAACCT | 55819 |
| rs755600128 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983139 | TTCCCCTCACTTTAT[A/G]GCAGTTTTTAATTTG | 55819 |
| rs755656007 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058486 | CGAATTCATAGAGAC[A/G]GAAAGTAGAGTGGTG | 55819 |
| rs755660374 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945457 | CAAGGAAAGAGAAAA[C/G]ATTGCTGAGCAACAC | 55819 |
| rs755675298 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070146 | GGCTACCATTGTTAG[G/T]TGCCAGTCTGGCAAC | 55819 |
| rs755697818 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058944 | AAATGTACTTACCAT[A/G]ACTTAACAGTTAGAT | 55819 |
| rs755709024 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976047 | TAAAAAGAGGGCCAG[A/G]CGTCAGGCTCATGCC | 55819 |
| rs755712709 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002174 | CGTGGCGCTGCTTCA[A/G]CTGAGACACTGGGGA | 55819 |
| rs755748277 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944295 | AAATTTTAAGTCCTA[A/C]GTGTTCAGTGCTATT | 55819 |
| rs755768520 | snp | C/T | 5.14002e-05 | 0.00506927 | intron-variant | RNF130 | GRCh38.p7 | 5:180040412 | TAAAGCAATGATTTC[C/T]AAGAAGAAAAACAAA | 55819 |
| rs755770509 | snp | A/G | 1.65272e-05 | 0.0028746 | missense | RNF130 | GRCh38.p7 | 5:179966862 | TCCCCATCCTGAGGA[A/G]GAGGTGAGATCCCCG | 55819 |
| rs755775291 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987055 | GTTTTTGGTGAACTC[-/TT]TGTTTTTTTTCTACA | 55819 |
| rs755784795 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930867 | AACATAACAAAACCC[A/G]GTCTCTACTAAAATT | 55819 |
| rs755803876 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014065 | CAGGCTTCAACATTC[C/T]GGACCAGTTTGGCAT | 55819 |
| rs755835029 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001490 | GGACCTAAGAGTCTA[C/T]TTTGTAGCTGTGATT | 55819 |
| rs755886949 | in-del | -/AAAT | 1.81417e-05 | 0.00301173 | intron-variant | RNF130 | GRCh38.p7 | 5:180013322 | AGTGCCTGCAATATA[-/AAAT]AAATATATAACTCAA | 55819 |
| rs755889474 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046114 | CACGAGAATCTGTGC[A/G]CGGTGGACCGCGGCG | 55819 |
| rs755898829 | in-del | -/TATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960064 | TAAAAATAATAAAAA[-/TATT]TATTTTTCTTATTTT | 55819 |
| rs755918814 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934659 | AGTGATCCTGCTGCC[C/T]CAGCCTCCCAAGTAG | 55819 |
| rs755934472 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005671 | GATGAAGTCTTAATT[A/C]ATCCTTTAAAATTCA | 55819 |
| rs755942351 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068707 | TAAATCAATCCACAG[C/G]TTCAAAATGAGCCAT | 55819 |
| rs755952097 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965223 | CTGGCAGCATTTCCA[C/T]AGTGCCCCCCTGCAG | 55819 |
| rs755952278 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958207 | TAGACAAGTGTTTCT[A/C]AAAACTAAAGCATAC | 55819 |
| rs755972733 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982067 | TAATTCCCTCCTCCC[A/G]CCACCCCATCCCTCC | 55819 |
| rs755978447 | in-del | -/ACTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019193 | ATCAAAACCATCCTG[-/ACTA]ACACGGTGAAACCCC | 55819 |
| rs755984499 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968190 | CTCCCAGCTACTCGG[A/G]AGGCTGAGGCAAGAG | 55819 |
| rs755994710 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936920 | ATGCAAAAAAATGGC[A/G]TTGGACCCTACTTCA | 55819 |
| rs756040298 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968852 | CATTTAGATGCTGCT[A/G]AACGGTCTACGATGC | 55819 |
| rs756062985 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039612 | TGGGGAAGTACCAAC[A/G]ACTCTCAATTAAGGT | 55819 |
| rs756073304 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962813 | ATTCCCAGTCCTGAG[C/T]GTGCCCTACAGCAAA | 55819 |
| rs756073346 | snp | A/G | 1.64749e-05 | 0.00287005 | intron-variant | RNF130 | GRCh38.p7 | 5:179980226 | TGCAAATAAAAACAG[A/G]TACTAAGTGTAAGAT | 55819 |
| rs756121697 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031187 | GTCAACAGCAAGCTA[-/T]TTAGTAATTAAATTT | 55819 |
| rs756126875 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042943 | ACAGGTGACTGAAAT[G/T]CTCCCATCTTTAATT | 55819 |
| rs756151553 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997990 | GAGACTACAGGTGCG[C/T]GCCACCACACCCAGG | 55819 |
| rs756161564 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023664 | AGAGTTGTACTGTAC[C/T]ATAATCCAGAGTGTA | 55819 |
| rs756172492 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995264 | CCACAGGAATCAGAC[A/C]GACCATATATCTGCC | 55819 |
| rs756227466 | in-del | -/AAGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036845 | CCCCACACTCAGCTT[-/AAGA]AAGAAATAAAACATT | 55819 |
| rs756229087 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948206 | ATCTTCTCTCATTCA[A/G]ATATTGCGAAGATTA | 55819 |
| rs756234397 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945971 | TATCACTCCCCACGG[C/T]CGCATCTGCCCAGCT | 55819 |
| rs756298697 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070164 | CCAGTCTGGCAACAC[-/TG]TGCATCTCAACCACA | 55819 |
| rs756309892 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971837 | TGGGATCTGGAACAA[A/C]CATTCATGCTTACAA | 55819 |
| rs756310208 | snp | A/G | 1.65677e-05 | 0.00287812 | intron-variant | RNF130 | GRCh38.p7 | 5:179955674 | ACCATTCTACCCTAT[A/G]GAATAAAAGGAAAAA | 55819 |
| rs756316979 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961133 | AAAAAACACAACACA[G/T]AAAAGCACAAATTGA | 55819 |
| rs756348465 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023538 | AAAAACTAAACTAAA[C/G]CAAAACAAAAAAACA | 55819 |
| rs756348481 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051828 | AATACAAATCACTTT[C/G]CATGAAAAGTCAATT | 55819 |
| rs756369842 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990382 | GATCAAAGACTTTAA[C/T]ACTTTCACTAATTTT | 55819 |
| rs756380531 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999473 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAAACCA | 55819 |
| rs756471142 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030823 | TGGCTTCTTTCGTTT[A/G]GCATAATGCTTTTGA | 55819 |
| rs756503394 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989339 | ACAGCCAAATCGTAT[A/C]AGCCGGATACTGAAT | 55819 |
| rs756507249 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952246 | TAATGAAATAGAGAA[C/T]AGAAGAGAGAAAAAT | 55819 |
| rs756558741 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066185 | CCCAGTGGGAGATAA[C/G]TGGAATCATGGAGGC | 55819 |
| rs756564740 | snp | A/G | 0.000104386 | 0.00722372 | intron-variant | RNF130 | GRCh38.p7 | 5:179970516 | ACATGCCTATAAAAT[A/G]ATGGAGAATTATGTC | 55819 |
| rs756577529 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046564 | CAGAAGTGATAGCCT[C/T]GGACAGTATTTTTCT | 55819 |
| rs756587789 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041320 | CCCACAACTCCGTAT[C/G]AAGATACACTTACTG | 55819 |
| rs756587948 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053201 | GGCATGGACAGGGAT[C/T]GCAACCACCTAGAGC | 55819 |
| rs756619633 | snp | C/T | 3.30169e-05 | 0.00406293 | intron-variant | RNF130 | GRCh38.p7 | 5:179978160 | AGGAGGCATACAAAG[C/T]ACATTAATATCATTC | 55819 |
| rs756640230 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953816 | CTACCAAGAAAGTGA[A/G]TAAATAGTTTAGAGA | 55819 |
| rs756668379 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990994 | TCGGTCTCTTGCCTC[A/G]GCACCTGGGTGGCTT | 55819 |
| rs756681504 | in-del | -/GT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935516 | AAGATATGTCAGCAC[-/GT]GTGTGTGTGTGTGTG | 55819 |
| rs756683502 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979564 | GGGGCAGCACTAAGA[C/T]GCAACTGTGTCCTTC | 55819 |
| rs756707948 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039559 | AAGTCAGAGGGCACT[A/C]AAGTTGAAATCCATC | 55819 |
| rs756723185 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994982 | GGAGGGGACTGGTGG[A/G]GAGAGGTGAAGCTGG | 55819 |
| rs756731008 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956792 | CCACATCAGTACGCA[C/T]ATGAGGGCATAGCCC | 55819 |
| rs756742374 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025854 | TTACTCATTTTCTTG[A/G]TAGGCATTTAGAATA | 55819 |
| rs756759761 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011339 | TGTATTATATCAATG[A/T]TAATTTACTGATTTT | 55819 |
| rs756770588 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922659 | AAAAAAATTCTAGGC[C/T]GGGCACAGTGGCTCA | 55819 |
| rs756777314 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943488 | TTTATTTTTTGCCAT[C/G]TGCACTTATTACTTA | 55819 |
| rs756787882 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929501 | ACCTGTAATCTCAGC[A/T]CTTTAGGAGGCCAAG | 55819 |
| rs756824824 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068600 | GACTATTTGCTCTTT[A/G]AAGGGATAGGACAAA | 55819 |
| rs756837369 | in-del | -/GATAAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977899 | AAACAAACATAAAAA[-/GATAAAC]GAAACCATAGAACAA | 55819 |
| rs756845556 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012687 | TGGGAAAGAATTTCA[C/T]ATAGGAAGGGGAAGA | 55819 |
| rs756865506 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956362 | AAGCTTTGGTTATTA[C/T]ACAACTCTCTAGCAA | 55819 |
| rs756871270 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929384 | TCTTGATTTCCAGTA[C/T]CTAAGTCCTTTTGCT | 55819 |
| rs756874266 | snp | A/C | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955479 | ACTCAACAGCACAGA[A/C]TTTTTATTTTATTAT | 55819 |
| rs756906616 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944223 | ATCTGCCTGCCTTGG[A/C]CTCCCAAAGTGTTGG | 55819 |
| rs756959254 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943247 | CAGGTCACTGACCAA[C/T]AGGTGACTGGTTTTA | 55819 |
| rs756988354 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957412 | GCGAGACCCTGTCTC[A/G]AATAAATAAATAAAA | 55819 |
| rs756995404 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988216 | TCTCTAGGTTTTCCA[C/G]TATGTTAGTGTATAA | 55819 |
| rs757003897 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954258 | GGGACATATCAAAGA[G/T]AACTGAAAATATATG | 55819 |
| rs757020132 | snp | G/T | 2.05937e-05 | 0.00320881 | intron-variant | RNF130 | GRCh38.p7 | 5:179963461 | AATCCAAAAACAATT[G/T]GTTACTTACTCATTA | 55819 |
| rs757027966 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934964 | TGCTTCGAACTTTTC[A/G]CTAGGCTTTCGAGAT | 55819 |
| rs757075852 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017815 | TTGGGCTCCGGAATC[A/G]GAGGGTCTAGGTTCA | 55819 |
| rs757079335 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998801 | CTAAGAGTGGGGTGT[C/T]GAATTCCCCAACTAT | 55819 |
| rs757126017 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021129 | TACCACCAAACCCGG[C/T]TCATTTTTTTGTATT | 55819 |
| rs757126025 | snp | A/T | 1.64852e-05 | 0.00287094 | missense | RNF130 | GRCh38.p7 | 5:180013105 | TGATCTTCTGAATGA[A/T]GTAGAATATGAGCCA | 55819 |
| rs757130617 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015885 | TTTGGGAAAAGAAGT[C/G]TGTAATTATTTCAAC | 55819 |
| rs757137742 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949396 | CCTGAGTAGCTAGGG[C/T]TTATAAGAACAAGCC | 55819 |
| rs757185031 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004383 | AAAACCACAGAAAGG[A/C]ATCATTTTACAAAGG | 55819 |
| rs757199197 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938665 | ATATTTAAATAATTG[C/T]CAAAATTAAGTTGCC | 55819 |
| rs757231867 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978168 | TACAAAGCACATTAA[C/T]ATCATTCTTTCTCAA | 55819 |
| rs757244360 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924424 | CACTTGAACCCAGGA[A/G]GCGGAGGTTGCGGTG | 55819 |
| rs757244839 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049573 | AGTATTACCATGTCA[C/T]AGACATGTTAAGTAT | 55819 |
| rs757252308 | snp | A/T | 3.29734e-05 | 0.00406025 | intron-variant | RNF130 | GRCh38.p7 | 5:179978187 | ATTCTTTCTCAAACA[A/T]ATGAAGTTGACATAC | 55819 |
| rs757265596 | snp | C/T | 0.000148245 | 0.00860815 | missense | RNF130 | GRCh38.p7 | 5:179966940 | CCGAGGGCTGATCTT[C/T]GGTTAACAGCTTGGG | 55819 |
| rs757283554 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007325 | AGAATTGCTTAAGCC[A/G]AGGAGGCAGAGGTTG | 55819 |
| rs757287548 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022633 | GTACACGGAGCTCAC[A/G]TGACTGAAGGTTCCC | 55819 |
| rs757307873 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064806 | CTAGAATTAAGTCTT[C/T]CATGCTTTAACTACA | 55819 |
| rs757320548 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968017 | ACTTAACAAACAGGC[C/T]GGGCGCGGTGGCTCA | 55819 |
| rs757370692 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921575 | GGCCAAGGCGGGTGG[A/G]TCATTTGAGATCAGG | 55819 |
| rs757390785 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981684 | CTTTCCTAACAAAAG[-/T]TAACAATGATTAATC | 55819 |
| rs757393824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939749 | GAAAGCGGAGAAAAA[C/T]GACCCCCTCCCTTGG | 55819 |
| rs757455016 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959926 | CTACCGTTCTCTGCA[A/G]ATCTTAGAACGTGAT | 55819 |
| rs757466213 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996629 | TTATGGATTTGCATA[C/T]GTTGAACCATTCTTG | 55819 |
| rs757484834 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971455 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC | 55819 |
| rs757534833 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948603 | TTGAACCCAGGAGGT[G/T]GAGGTCGCAGTGAGC | 55819 |
| rs757536278 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033340 | GTGCAATTCTTACAT[G/T]TCTTTTTAACAAGTT | 55819 |
| rs757561323 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054345 | CATTATATCACCAAA[C/T]GCAAAGAATTCCTTC | 55819 |
| rs757575796 | in-del | -/TTAAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985072 | TCAAGTCATCTCCTA[-/TTAAT]TTAATTACTCTGGTG | 55819 |
| rs757588263 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971678 | CCGGCCAAGATAAAA[G/T]AAATTTTTAAGTAAG | 55819 |
| rs757597157 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045334 | CCCTCACGGTGTTAC[A/G]GTTCTTAAAGATGGT | 55819 |
| rs757611582 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052077 | TCCATCAAGTTTTCC[C/T]CCCACCTCTCTAACT | 55819 |
| rs757611583 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963688 | CCAAGATTGGCCCAA[A/G]GAAGTGAAGCAGGAG | 55819 |
| rs757625701 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001405 | AATGTATTTGTGGCA[C/G]CTGTGGCAAAGTGGG | 55819 |
| rs757660953 | snp | C/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180074041 | TGCCCATGACCCCTG[C/G]CACAAGAAACAATTA | 55819 |
| rs757671475 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939453 | CTTCTGTAGCTGAAC[-/AA]GTTTTTGTTCGATGA | 55819 |
| rs757725827 | snp | A/G | 3.31411e-05 | 0.00407056 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015313 | TGGTATAAGATACCA[A/G]GTATGGCTATAAAGT | 55819 |
| rs757730866 | snp | A/G | 6.83585e-05 | 0.0058459 | intron-variant | RNF130 | GRCh38.p7 | 5:179978337 | TGCAAGTATATAAAT[A/G]GTTGGGATGCAATTC | 55819 |
| rs757734433 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950809 | CATTAAAAGTCCTAC[A/G]CCTCCTGATGTACTT | 55819 |
| rs757741030 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049847 | CTGCCTCTGAATATA[C/T]TGACCGAATTTCATT | 55819 |
| rs757837790 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937905 | TGCTTTCAATGAATC[-/TG]TGTGTGTGTGTGTGT | 55819 |
| rs757847385 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034803 | CCTCCTAGTGAGTCA[C/G]TGAACCTGTGGATGG | 55819 |
| rs757848744 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931234 | GTAACACTGATGGCG[A/T]TACAGTGTGGGGTGC | 55819 |
| rs757855237 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004232 | TAAATGAAGTACAAA[C/T]CCTGGTTTCAAAGCA | 55819 |
| rs757887135 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930765 | GAATGGAGGCTGGGC[A/G]TGGTGGCTCATGCCT | 55819 |
| rs757891185 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002154 | ATGCACCACTTCCTG[A/G]GAGGCGTGGCGCTGC | 55819 |
| rs757896535 | snp | C/T | 1.6625e-05 | 0.00288309 | missense | RNF130 | GRCh38.p7 | 5:180013285 | CCCTCAATTCTGTTA[C/T]CATGACAGCAATAAT | 55819 |
| rs757898395 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921242 | ATATCCATTACCCCA[A/G]AGTTTCCTGGTGCCT | 55819 |
| rs757898503 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037243 | ATGCACATGTGCGAG[A/G]GTAACAAGGGTGGAA | 55819 |
| rs757920504 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067337 | TGCAATTCTGACCCT[A/G]CTATCAAATATATGT | 55819 |
| rs757930480 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956086 | TTTTGAAGTGATAGG[G/T]ATGTATGGCTGTCTC | 55819 |
| rs757988144 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934838 | TTACAGGCATGAGCT[A/G]CCATGCTCGGCTTGG | 55819 |
| rs758030020 | snp | A/G | 0.000164731 | 0.00907405 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966912 | GCCAAGGGAGTTGTC[A/G]CCGGCGAGGTCGCCG | 55819 |
| rs758044049 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980761 | GGTGTACTTACCTTC[C/G]AGGGTTGAGCTGTTT | 55819 |
| rs758050921 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038123 | CAGTGGTGTGATCAC[A/G]GCTCACTGTAGTCTC | 55819 |
| rs758158323 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981513 | ATGTATCTAACATCC[A/G]GCTTCCATTACCAGT | 55819 |
| rs758187814 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024291 | TGAATAAAGTAATAG[A/G]CTTTGGTTAATAATT | 55819 |
| rs758225158 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059246 | ATATCTGCTCATGCT[A/G]CCGTCTCAGCTGAAA | 55819 |
| rs758228207 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945988 | GCATCTGCCCAGCTG[C/T]GAGTGACAGAAGCAT | 55819 |
| rs758229881 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960951 | ACGAATAATTACAAA[C/T]TTGTTTGCTAAAATA | 55819 |
| rs758259332 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038480 | GATTACAGGTGTGAG[A/C]CACTGCGACCAGCCA | 55819 |
| rs758260215 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060614 | CCTAACTTAGCGCAG[A/G]GATTCTTAACTTGGG | 55819 |
| rs758262729 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000793 | GTTTCCCCAACTCTA[C/T]TGATTGTCTACACGT | 55819 |
| rs758275601 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042679 | CTGGTTTTAGGTGTT[C/T]TGTTCGTTATTTTTC | 55819 |
| rs758287290 | snp | A/G | 1.72988e-05 | 0.00294093 | intron-variant, synonymous-codon | RNF130 | GRCh38.p7 | 5:179963533 | TGTGAGGGCACTGAG[A/G]AGGCCAAAACTGGCA | 55819 |
| rs758295965 | snp | C/G | 5.48276e-05 | 0.00523553 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071631 | GTTGTCTGCCCGTGC[C/G]GGCCACAGGCTGCAG | 55819 |
| rs758342138 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017691 | CATCCCCATCAATTC[C/T]ATTTTTTAATGAGGA | 55819 |
| rs758352647 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947872 | CATACAGTATATCTA[C/T]ATACACAGACCATAT | 55819 |
| rs758363787 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989468 | TTTTGAATTGTCATA[A/T]CCTCCTGCAGAATTG | 55819 |
| rs758370473 | in-del | -/TTGT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180033773 | ACATTCTTTCAAGAC[-/TTGT]TTGTTTATTACATCT | 55819 |
| rs758398594 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965973 | GACGTGCTAGGCAAG[C/T]AGCAGCAGGTGCTGG | 55819 |
| rs758402776 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975197 | ATAGGGGCGGGGAGG[A/C]GTCCCAAGGCAGAAG | 55819 |
| rs758420404 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034624 | ATTTGTCAGTATACA[C/G]AAAAAAGTAAACATA | 55819 |
| rs758437785 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034617 | GTGTCTAATTTGTCA[-/G]TATACAGAAAAAAGT | 55819 |
| rs758446920 | in-del | -/G | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015665 | AGTAGGAAAGGAGTA[-/G]GGAAAGGAGTAGGGA | 55819 |
| rs758471623 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020157 | ATGATGAGGCCCAGG[A/G]AGCAGCTATGGGACC | 55819 |
| rs758519282 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965415 | TCATGTGCAAATTCT[A/G]CTAAAGGTGATTAAT | 55819 |
| rs758529452 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937365 | AACAGCAAAAGACAA[C/T]CTGATTAAAAAATGG | 55819 |
| rs758564611 | in-del | -/GTGAGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937932 | TGTGTGTGTGTGTGT[-/GTGAGA]GAGAGAGAGAGAGAG | 55819 |
| rs758571279 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986715 | TGCCATGTATTTGTT[G/T]TAATAATTTTTAACT | 55819 |
| rs758590579 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005738 | CCTTGACTCCCTGAG[A/G]GTAATATCACTCTGC | 55819 |
| rs758595997 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062616 | AATAGGGATATGAAG[A/C]CTAAAGGTTAGAGGA | 55819 |
| rs758605795 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968931 | ATGCCCGATACTTTG[A/G]GAAATCCCATCACTA | 55819 |
| rs758628802 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984624 | GATGAATTTATATAT[A/G]TTGTTAAATATAATT | 55819 |
| rs758631352 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007291 | CTTTAGTCCCAGCTA[C/T]GTGTGAGGCTGAGGC | 55819 |
| rs758632791 | snp | C/G | 4.18962e-05 | 0.00457672 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071704 | CCCGCGCAGCTCATC[C/G]TCCCTCCGGCAGCCG | 55819 |
| rs758634115 | in-del | -/CTG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025343 | TACCTTCCTCCTCTT[-/CTG]CTGCCAGTGAGGAAA | 55819 |
| rs758656308 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040547 | CCGTGATATTTTCTC[C/T]TTAAACGTGCAGTTT | 55819 |
| rs758657664 | in-del | -/TGAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937933 | GTGTGTGTGTGTGTG[-/TGAG]AGAGAGAGAGAGAGA | 55819 |
| rs758680635 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004769 | TCAGGTTTTGCCATT[C/T]GGCAATCAGAACTCT | 55819 |
| rs758699097 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025657 | AAAAAATGTATGAAC[C/T]AGATGGAAGATACAG | 55819 |
| rs758707422 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056389 | GAAGGGAGCCACAGA[C/T]CAGAGGAGGCTGCAA | 55819 |
| rs758721939 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951028 | GAGAGTCCACTCTAG[A/G]AAATAAGGCCAAACA | 55819 |
| rs758742192 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973413 | TGTGGCCTTTTCTTC[C/T]CTTCTAGGCAAAGTT | 55819 |
| rs758758207 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943149 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCC | 55819 |
| rs758773317 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948735 | GCATAACTAAATAAT[C/T]TGGAAGATAAAAAGT | 55819 |
| rs758794351 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011039 | GAAGGGGATAAGAGA[C/T]ATCTTTGTATTTGTA | 55819 |
| rs758816128 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981603 | ATGGCAAGCATCACA[C/T]AATTTCACCCATAAA | 55819 |
| rs758817599 | in-del | -/AAAGG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987575 | CTTGAACCAGTTCTT[-/AAAGG]AAAGTCTTTCAGCTT | 55819 |
| rs758845297 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009882 | GAGCAATTAAACAAA[C/T]GGTGGTACATCCAAA | 55819 |
| rs758851076 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054986 | TTATTGATCTTTTAT[C/G]TATGGGTGTTCCTAA | 55819 |
| rs758863258 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930136 | GATCTTGGCTCACTG[C/T]GACCTCTGCCCCCCG | 55819 |
| rs758884418 | snp | A/G | | | intron-variant, synonymous-codon | RNF130 | GRCh38.p7 | 5:179963545 | GAGGAGGCCAAAACT[A/G]GCAATAATAAACCAT | 55819 |
| rs758906233 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052185 | CACTCCCCTGCCTTC[A/G]ACTACCACCTGTGTA | 55819 |
| rs758909493 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988688 | GTTGTTTAGTTTCCA[C/T]GTAGATACTGTTTCC | 55819 |
| rs758926316 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031358 | TGGGCATGGTGGCAC[A/G]CACCTGTAATCCCAG | 55819 |
| rs758933747 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060511 | CGGCCATCCTTGAAG[A/G]GTGCTGATTAATGGA | 55819 |
| rs758946040 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021993 | GACCTTGGCACTTTC[A/G]AAGACTACATTCGGC | 55819 |
| rs758959015 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044920 | GGGTGCCAACACGAA[C/G]TGCACTTAAGAGACT | 55819 |
| rs758978071 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973832 | ACGGAAAGCAGGTAA[C/T]GTGGACAGTGAAACC | 55819 |
| rs758984912 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043635 | ACACAGCAAGGGGTG[C/T]AACCACAGAGCAAAA | 55819 |
| rs758990573 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000356 | TCTCGACAATTTGAC[C/T]GTAATGTGACACGGG | 55819 |
| rs759021669 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999862 | ATTCAAGGTTATTAC[C/T]GGTAGGTGAGGACTT | 55819 |
| rs759053430 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938168 | TTGCCACGTTGCCCA[A/G]GTTGGTCTTGAACTC | 55819 |
| rs759108882 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020893 | TTCAACACAACACAG[A/G]AACTCCCACAAATTA | 55819 |
| rs759112319 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961890 | GGCACTGCAGTGGCA[C/T]TGGCTTGGCTAACAT | 55819 |
| rs759121328 | in-del | -/ATTAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986617 | GGTGGCTATGAAATT[-/ATTAC]ATTAATACAGTACGT | 55819 |
| rs759147292 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179980168 | GGTTGTCAATTTACT[G/T]ATGGCTTTCTTGGCT | 55819 |
| rs759162289 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046321 | AAGGGCTCCTCAAGC[A/G]TGGCCAGAGCAGACA | 55819 |
| rs759177570 | in-del | -/GT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068311 | AAGCTCACCATTTGA[-/GT]GTAAGTAATAAGAAA | 55819 |
| rs759182159 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004166 | AAAGTGCTCCAGCCC[C/G]TAAAAGGAGCTCTCA | 55819 |
| rs759186500 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949904 | TACTCACTAGCCTCA[C/T]GTGGAAAATGGTATA | 55819 |
| rs759217816 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018691 | TCTAACCACAGATTT[C/T]TGGATGCCCATTCTC | 55819 |
| rs759220454 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925609 | TCCTAGCTCACTGCA[C/G]CGTCAACCTCCTGGG | 55819 |
| rs759222220 | in-del | -/ATTAAATTCTCCAGTGCTATAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986030 | CTAACGTTTGCTGCC[-/ATTAAATTCTCCAGTGCTATAT]CCTTTGCTTTCCTTT | 55819 |
| rs759241042 | in-del | -/GGC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968324 | CAAACAAAAAAAGAA[-/GGC]GGCGGCTAGCGGTAA | 55819 |
| rs759259611 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023222 | GCAGATGATTACAGA[C/T]AGAAATATTTATAGA | 55819 |
| rs759279112 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031981 | TGTTTTGGTTGCACT[A/G]TTGTTTTGATTGCAT | 55819 |
| rs759293908 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979283 | TTTCTTTGGTGTACA[A/G]TAAAGTTCACTAAGA | 55819 |
| rs759295317 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988564 | TCCCTCTTAGCACTG[C/G]TTTTGCTGTATCTTG | 55819 |
| rs759296996 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987886 | CGTACTGGGTTGAGG[C/T]TTTTTGTGTCTATGT | 55819 |
| rs759297045 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975119 | GTGAGGGAACAGAAC[C/T]GCTTAGCAACATGAG | 55819 |
| rs759367946 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065626 | TTAGCTGGGTGTGGT[C/G]GTGGGCACCTGTAAT | 55819 |
| rs759380669 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054158 | TGTTACCTATTTTTA[A/C]TTCATTTCAGTAGAA | 55819 |
| rs759387963 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952687 | AATTGGTTCAATGTA[A/G]GAAAATCAATGTAAT | 55819 |
| rs759412317 | in-del | -/TAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990895 | CTACAAACTAATGAT[-/TAA]TGATATTCATATATA | 55819 |
| rs759433831 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065587 | AACATGGTGAAACCC[C/G]GTCTCTACTAAAACT | 55819 |
| rs759458665 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954328 | TCATAACAGCCGAAC[A/G]GCGGAAACAAGTCAA | 55819 |
| rs759462789 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939187 | GCGCCACTGCACTCC[A/T]GCCTGGGATACAGAG | 55819 |
| rs759492182 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969549 | TCTTCATCCCATACT[C/G]ATCGACCAACAGAAG | 55819 |
| rs759497080 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | RNF130 | GRCh38.p7 | 5:180040519 | CTACAGCAACTGCAT[C/T]GTGGAAAGCGGCCCG | 55819 |
| rs759536466 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009421 | AAAACAATCTAGGTA[G/T]AAAATGGGCAAAAGA | 55819 |
| rs759545024 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980307 | TTTTACTACATCCCT[C/T]TCCATGTCCTACATA | 55819 |
| rs759591890 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012217 | TTCCGCTAGAAAGAG[G/T]AAGGATAAAAATCCC | 55819 |
| rs759635543 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015115 | GTTTACCAGAATACC[A/G]ATTAAAAATCTACAA | 55819 |
| rs759642545 | in-del | -/AAGTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953651 | TCATCAAAGATCTAA[-/AAGTT]AAGAGCAAAGACTAT | 55819 |
| rs759645607 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001970 | AGCTCATCCCTGGCA[G/T]GCACAACTGCTCAGT | 55819 |
| rs759658051 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968809 | GGAGACATTTCTGAC[-/T]GTCGTGGCTGTGGTG | 55819 |
| rs759667921 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046043 | AGTGGCGTGGACGGA[-/G]GGGGGTGGGGCTCGG | 55819 |
| rs759696542 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013508 | ATTTGTTGTGTGGTA[C/T]TTAAGACTTAAACAG | 55819 |
| rs759704189 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982453 | CTGACTTTTATTTAA[A/G]AGACTGCCAAAGTGT | 55819 |
| rs759705482 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930348 | GGCATGAGCCACTGC[A/G]CCCGGCCAAAAATTT | 55819 |
| rs759729030 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958749 | TGGAGTGCAATGGGG[C/T]GATCTCGGCTCACTG | 55819 |
| rs759729522 | snp | C/G | 2.47424e-05 | 0.00351718 | intron-variant | RNF130 | GRCh38.p7 | 5:179963441 | TGGGATCATCTGGCA[C/G]ATGCAATCCAAAAAC | 55819 |
| rs759731128 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973788 | ATAAAAAACAGGCCC[A/G]CCACACACAGGGTGG | 55819 |
| rs759813938 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036114 | GTTGAAAAGTGAACA[-/T]TTTAGACAGTATATT | 55819 |
| rs759817934 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045948 | GGATCCCGTGCGGCA[C/T]GCCCACACTCCTCAG | 55819 |
| rs759819912 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | RNF130 | GRCh38.p7 | 5:180013215 | ATTCGAGTTCCAACA[C/G]CTATTGTCATTTGTA | 55819 |
| rs759826324 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000954 | TTTCATGTTTCTCAC[A/G]TCCCTGTGTTGATGT | 55819 |
| rs759829436 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974236 | ACATCTGCAGCGGCC[A/G]GCCCCCCGCTTTAGC | 55819 |
| rs759836001 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005024 | TCTCTACATAACCTT[A/G]TTTTATTAATATCAT | 55819 |
| rs759860802 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926850 | ACCCTGGGGGACCTG[A/G]TGCCATTTCCAGGTA | 55819 |
| rs759872679 | snp | A/G | 2.59555e-05 | 0.00360237 | missense | RNF130 | GRCh38.p7 | 5:180071591 | CCGTCACGTTGATGA[A/G]CGCCGTGTAGTACTC | 55819 |
| rs759907946 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955140 | GGGGCACAGTGGGGA[A/G]CAAATGTTACAAGTC | 55819 |
| rs759935091 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038035 | TAGATTACTCAAAAT[A/T]AAACAGGGTTTTTTG | 55819 |
| rs759945094 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049086 | CAGCTCACTTCAAAC[C/T]TCAAGGTAACCTTAT | 55819 |
| rs759959399 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936152 | CTTGAGACAGGGTCT[A/C]GCTCTGTCACCCAGG | 55819 |
| rs759974289 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922253 | CGTGTATCTTCGTTT[C/G]TGAAGTGTTTTGTTC | 55819 |
| rs759994319 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921070 | TGCTACTCAAAGCTG[A/G]GCTGTGCTTACATTT | 55819 |
| rs759995688 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943099 | ACTCAGGAGGCTGAG[A/G]TAGGAGAATTGCTTC | 55819 |
| rs760011630 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995565 | GGACTGAGACTGGAG[C/T]CCTCTTATCAGCCAC | 55819 |
| rs760014407 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967650 | TTCCGTTGTAACAAT[A/G]TGGCTATTTGTTTAC | 55819 |
| rs760031387 | in-del | -/AGTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011987 | CAATAAACTGCAGTC[-/AGTA]AGTGTTTGGGTATTT | 55819 |
| rs760076854 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001844 | CAGCTGAGCTTCTTG[A/T]AGACTAGTACAGGTT | 55819 |
| rs760076932 | snp | A/G | 0.000136874 | 0.00827153 | intron-variant | RNF130 | GRCh38.p7 | 5:180071422 | TACGCGGGATGCAGC[A/G]ACCACCGCCCGCCGC | 55819 |
| rs760082804 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960715 | ATTCTAGTAGGTATA[C/T]GCATAGAGGTGGAGT | 55819 |
| rs760093406 | in-del | -/AAAC | 1.70892e-05 | 0.00292306 | intron-variant | RNF130 | GRCh38.p7 | 5:180040421 | GATTTCTAAGAAGAA[-/AAAC]AAAATCAACAACCCT | 55819 |
| rs760102997 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026566 | ACAGGGCACTGGAAC[A/G]GACGTCCTTCAGTCA | 55819 |
| rs760103493 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053964 | CCTCCCGAGTAGCTG[C/G]GACTACTACACCCAG | 55819 |
| rs760133352 | snp | A/T | 2.78858e-05 | 0.00373392 | intron-variant | RNF130 | GRCh38.p7 | 5:179966787 | CATGCCCTGTGCCTG[A/T]GCGGAGGCCCCCACT | 55819 |
| rs760164388 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039099 | TTCCCTGAATAAATT[A/C]AAAGTTACACGACCC | 55819 |
| rs760174635 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971197 | TTAAAAAAAGGAACT[C/T]GTGCCCTCCGGAAGA | 55819 |
| rs760205290 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997409 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 55819 |
| rs760226713 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000497 | TAATGCCTTTCCCCT[-/TC]TCTCTCCTTCTGGAA | 55819 |
| rs760235139 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041169 | AATTCAACCATGTTA[A/G]AGCAAATTTCTTCAT | 55819 |
| rs760235615 | in-del | -/AAAAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977878 | AATAAATAAATAAAT[-/AAAAG]AAAACAAACATAAAA | 55819 |
| rs760250683 | in-del | -/AAGAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067408 | TAGAAGACCTTCACA[-/AAGAG]AAGAGCAGCAGGAGG | 55819 |
| rs760302807 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959397 | CTTTGGGAGGCCGAG[A/C]CAGGTGGATCACAAG | 55819 |
| rs760310480 | snp | C/T | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180014869 | CACATGTCTGTGGTC[C/T]CAGATACTCAGGAGG | 55819 |
| rs760312108 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031248 | TCCTAGCACTTTGGG[A/T]GGCTGAGGTGGGTGG | 55819 |
| rs760314441 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992148 | AAATCATTGTTTTTT[-/G]CTTTTTGTTTTGAGA | 55819 |
| rs760314959 | snp | C/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072665 | GTGGGCAACCTAGGT[C/T]CCAAGCATGCGCAGT | 55819 |
| rs760348807 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967747 | TGGTTGTGAGAAGTT[C/T]GTATGTTTATAGAGA | 55819 |
| rs760356592 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938138 | ATTTTTGTATTTTTT[G/T]GTAGAGATGGGGTTT | 55819 |
| rs760363461 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030255 | CATAAATACTTGCTT[C/T]GTCTCTCCAAGTAAG | 55819 |
| rs760435805 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998327 | TTCCTAATTTACTCA[C/T]TGACCCACTGGTTGT | 55819 |
| rs760446800 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951618 | TCGATCAGAATATGT[A/G]CATTCTTAAGTGCAC | 55819 |
| rs760482686 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035433 | ACCATATGGTCTATC[C/T]GAGAGAATGCTCCAT | 55819 |
| rs760494323 | in-del | -/CCG | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072132 | GCCTGAGGCGCGTGT[-/CCG]CCGCCGCCGCCCCGC | 55819 |
| rs760511656 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064666 | TCGCAACTAGAAACT[A/C]TCTCTTGAATCCCCA | 55819 |
| rs760515860 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952983 | CAATCTACTATTTGA[A/G]GTTCTAGCCAGAACA | 55819 |
| rs760520677 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990203 | GTTATTTATTGGATA[C/G]AAAGTAAAAGGGGCA | 55819 |
| rs760551563 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979061 | AATTGGCTTTAATAA[A/T]TAAAGGAAATAACTG | 55819 |
| rs760562861 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988663 | TCATCAACCTTATGG[C/T]AGTGATCATGTTGTT | 55819 |
| rs760611438 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939066 | AGACCCCATCTCTAC[A/C/T]AAAAATACAAAAATT | 55819 |
| rs760632776 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948362 | GTTTCACCGGGACTC[C/T]ATTCTTTGTTCTGTT | 55819 |
| rs760687964 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971519 | GGACTACAGCAGCCC[A/G]CCACCACGCCCAGCC | 55819 |
| rs760711075 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068091 | ATGCAAAGCAAGAAG[C/T]GGCCGATACTAAACT | 55819 |
| rs760758386 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943656 | TCAGAGAGATAAAAT[A/C]ACTTACTCAAAATCA | 55819 |
| rs760765260 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010075 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 55819 |
| rs760805076 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955871 | CTCATCCATCTTAGA[C/G]GTGCTTTAATACTCC | 55819 |
| rs760824334 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029902 | TGCCTAGGCTAGAGC[A/G]CAGTGGCACAATCTC | 55819 |
| rs760847530 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928356 | ATAATGGATATTTTG[-/T]TTTTTTTTTTTCATT | 55819 |
| rs760858857 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026477 | TAACTACATGACAAA[G/T]AACTCACTCTGCTAA | 55819 |
| rs760877486 | in-del | -/GGAGTACAGTGGCAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053878 | TCTGTCGCCCAGGCT[-/GGAGTACAGTGGCAC]GATCTCGGCTCACTG | 55819 |
| rs760884500 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000042 | CCAGTGACTTTCATA[C/T]TCCTGCATGTTTTCC | 55819 |
| rs760885714 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980489 | TAATTGCTGCATTTT[C/G]TGTCGAATAAACATT | 55819 |
| rs760890808 | snp | C/T | 1.66219e-05 | 0.00288283 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015253 | AACCGCTTTAAATTT[C/T]CCTTTAGAAATCTCT | 55819 |
| rs760956422 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017989 | TAAATACCTGAGACT[C/G]GGTAATTGAGAAAGA | 55819 |
| rs761006891 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972855 | TTAGTTATAAATATG[C/T]TTGGGTTCTTGAGTA | 55819 |
| rs761007406 | snp | A/G | | | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015302 | GCCATGATCTGTGGT[A/G]TAAGATACCAGGTAT | 55819 |
| rs761007589 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010783 | AAGAGTAGCACAAGG[G/T]TTCCTTGTGATGGAA | 55819 |
| rs761034304 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003442 | CCTCTGAACTTTGAA[C/T]ACCTCTTATAGCACA | 55819 |
| rs761036559 | in-del | -/T | 1.65873e-05 | 0.00287982 | intron-variant | RNF130 | GRCh38.p7 | 5:179955695 | AAAGGAAAAAAGAGG[-/T]CATAAATTAAAGAGT | 55819 |
| rs761057151 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991805 | TACAAATCACCATAA[C/T]GTAGAATCAGTAGGA | 55819 |
| rs761060271 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013533 | AAACAGACATAAGGC[A/G]TAGAACGACTGCAGT | 55819 |
| rs761069535 | in-del | -/AGAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948681 | CTCTGTCTCAAAAAA[-/AGAG]AGAGAGAGAAAAAAA | 55819 |
| rs761107657 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967442 | AAGCCCCATTTATCT[C/G]GTAGTCAGTTTTTAA | 55819 |
| rs761108669 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975876 | GGTTCAGATCAACCA[C/T]GGCCTGGACCTTGGT | 55819 |
| rs761110555 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004052 | GAGGAGATTGAGGCA[C/G]AGATTAAATAATTTG | 55819 |
| rs761127348 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959394 | GCACTTTGGGAGGCC[A/G]AGACAGGTGGATCAC | 55819 |
| rs761133233 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920706 | GGTTCCACTTAGAAA[C/T]GTGAAGACTTCTTCC | 55819 |
| rs761133344 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932622 | ATGGATGGATCACCT[C/G]AGGTCAGGAGATCAA | 55819 |
| rs761151354 | snp | C/G | 0.000146316 | 0.00855201 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071673 | GAGCGCGGCGAGCCG[C/G]GCAGGGCCCGCCCGC | 55819 |
| rs761184200 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982554 | CACCAACACTTGGTA[C/T]GGTGAGATTTTGTGT | 55819 |
| rs761220670 | snp | A/C | 1.86268e-05 | 0.00305173 | intron-variant | RNF130 | GRCh38.p7 | 5:179970552 | TTACATACCAAGAAA[A/C]TTATTAGGCCAAAAT | 55819 |
| rs761235463 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064457 | ACTTCCAACAGTTTT[C/T]AGTTCTTCTGGTGGT | 55819 |
| rs761238559 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023639 | CCAAAGCTAGGATAA[-/T]TTGAGTAACAGAGTT | 55819 |
| rs761264998 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052440 | ACTGCTGCTGCCACA[A/C]ATAGGGACACAAGGA | 55819 |
| rs761268126 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977972 | GGAGTCTGGAGGCCG[C/T]GTGCCACATCGCATA | 55819 |
| rs761323999 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003697 | GCCACTATTTTTTTA[A/G]AATTTTTCATTCTAA | 55819 |
| rs761325714 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980620 | AGGTGTGTAAATGCC[A/G]TCTTATTAAGGGAAA | 55819 |
| rs761344960 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959726 | GAGTTTATATATATA[A/T]ATTTCTACTACTACA | 55819 |
| rs761380140 | snp | A/T | 2.99021e-05 | 0.00386654 | missense | RNF130 | GRCh38.p7 | 5:180071572 | CCGCGGCCGGGCTCC[A/T]GCACCGTCACGTTGA | 55819 |
| rs761396556 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002669 | TCACCACAGTGAGCT[-/C]CTTCCTGGTTCCCAG | 55819 |
| rs761398487 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996098 | TCCTATCCATGAACA[C/T]GGGATGTCTGTTTTT | 55819 |
| rs761419741 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055667 | TACAGACGAAATGAT[A/C]CACTTTTTACTAAAT | 55819 |
| rs761447490 | in-del | -/ATC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933349 | TTTGTATTTTTCAAA[-/ATC]ATCAATTTATTTTCA | 55819 |
| rs761465467 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011480 | GTTAAGGTATATATA[-/TG]CAAAGGTTGAGGGTG | 55819 |
| rs761480153 | snp | C/G | 4.75986e-05 | 0.00487822 | missense | RNF130 | GRCh38.p7 | 5:180071467 | TCACCTCCGTGGAGG[C/G]GCAGCGGCGCCAGCA | 55819 |
| rs761493423 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959220 | AAGAGTCCTTCAAAC[A/C]CCTGGAAACAGCTCT | 55819 |
| rs761496485 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997203 | CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT | 55819 |
| rs761501227 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069843 | CAATACACATGAGTT[A/C]GTTTCCAATACCCTT | 55819 |
| rs761502041 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925011 | AGTTTCCTCTCTTCA[C/G]GATGAATTAAAGCTA | 55819 |
| rs761517194 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044663 | ACAGCGAAACCCCAT[A/C]TCTACTAAAAATACA | 55819 |
| rs761520363 | in-del | -/A | 1.89564e-05 | 0.00307861 | intron-variant | RNF130 | GRCh38.p7 | 5:179970558 | ACCAAGAAACTTATT[-/A]GGCCAAAATGGAAAG | 55819 |
| rs761547874 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051403 | TACAGGTGCCCGCCA[C/T]CACACCTGGCTAATT | 55819 |
| rs761579366 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007878 | CAGGGTGAGCTACAC[C/G]CAGTCCACTAACACA | 55819 |
| rs761600848 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073105 | ACCAGCCAGGGTTGA[A/G]TCTCCTGTCTCCTAC | 55819 |
| rs761648450 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971115 | GAGATTTTCTCTCTT[A/C]TTCAGGCAAGTAGAA | 55819 |
| rs761652488 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032874 | CTGTGATTTGCATAG[A/G]TACATACCACAAGGA | 55819 |
| rs761694146 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936732 | AGACTACTATAAAAT[G/T]ACAGTAAACAAGGCA | 55819 |
| rs761720989 | in-del | -/AAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958271 | TTAACGACTAATATT[-/AAC]AACAAGGCACAGGAC | 55819 |
| rs761742966 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989172 | CAGACGCTTATAAAA[C/T]TATCCCATCAGATCT | 55819 |
| rs761774116 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951198 | CAACAAAGCCCCAAA[C/T]TACATGAAGCAAAAC | 55819 |
| rs761811424 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035748 | CATTTTCCTTCAATT[A/G]ATTCTTCCCTCTACT | 55819 |
| rs761851910 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034279 | CTAGATTCTATTTGC[C/T]AATAATTTTAAAAGA | 55819 |
| rs761862793 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953610 | CCCCTACCTTACACC[A/G]TATACAAACATTAAC | 55819 |
| rs761883674 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019512 | CAGGGAGACTGCTGG[C/T]TCCTGATCCCAAGAC | 55819 |
| rs761903856 | snp | C/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955600 | AATGATGCACAAAAA[C/T]AGGTTCTTTTTTCCT | 55819 |
| rs761913127 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036782 | TCTAATGATTATTTT[A/G]AAATACTTCAAATAA | 55819 |
| rs761926144 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980401 | TAAAAAGTGTTAGAA[C/T]ACCCTGTTAGGTCAA | 55819 |
| rs761927508 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954442 | TGTATGAACCGTGAA[C/T]ACATGCTAAGTCAAA | 55819 |
| rs761930512 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990870 | ATAATATTGGAATAA[A/G]GAGTAATTGCTACAA | 55819 |
| rs761935691 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920477 | CACCAGGCTTGTGTT[C/T]CTCACATGGCTAGGA | 55819 |
| rs761949066 | snp | C/G | 7.14652e-05 | 0.00597725 | missense | RNF130 | GRCh38.p7 | 5:180071681 | CGAGCCGGGCAGGGC[C/G]CGCCCGCCCCGCGCA | 55819 |
| rs761965311 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006387 | ACAGGAATGTTCCAT[A/G]TATTTCCACATTCTG | 55819 |
| rs761966504 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047563 | CAGCCTGACCAACAT[A/G]GTGAAACCCTGTCTC | 55819 |
| rs761980001 | snp | A/G | 3.76982e-05 | 0.00434139 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966816 | CTTACTTGTTACTGC[A/G]ATGTTGATTTCTCCT | 55819 |
| rs761986367 | snp | C/T | 1.71278e-05 | 0.00292637 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015360 | ACAAACGACATATGA[C/T]AATCAGTCTCATTGC | 55819 |
| rs762003586 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066765 | CGGAACCCGGGAGGT[A/G]GAGGTTGCGGTGAGC | 55819 |
| rs762039749 | snp | C/T | 1.64836e-05 | 0.0028708 | missense | RNF130 | GRCh38.p7 | 5:179966883 | GAGATCCCCGAAGTT[C/T]GAAGTGGCTCAAGGC | 55819 |
| rs762044428 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030113 | TCGGCCTCCTGAAGC[A/G]TTGGGATTACAGGCG | 55819 |
| rs762070100 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023359 | CCGGATCTTGGTTTT[A/T]AATACCACTCTCCAA | 55819 |
| rs762078400 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973772 | ATAAAAACACACATA[A/G]ATAAAAAACAGGCCC | 55819 |
| rs762159805 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991654 | ACCTTTTTGGCACCA[C/G]TGACTGGTTTTGTGG | 55819 |
| rs762163391 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015850 | AATAAGAACACCAAC[G/T]AATTTCAACGGGAAA | 55819 |
| rs762199214 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013850 | GAACAAAAACAAGTA[C/T]AGGATACCAAGCTTT | 55819 |
| rs762208625 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936793 | GATTAATGGAATAAA[A/T]TTGAGAGTCCAGAAA | 55819 |
| rs762213535 | in-del | -/AGGAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977425 | GTTTTTGAAACCCAC[-/AGGAA]AGGAATCACAAAACA | 55819 |
| rs762247438 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059232 | CCCCTCTCAGTGTAA[C/T]ATCTGCTCATGCTGC | 55819 |
| rs762248345 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975039 | CTGCTGTGCCGAATG[C/T]GGAGCGCCAGCCAGG | 55819 |
| rs762252264 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027947 | CGCATCAACCTCATC[A/G]AGACCACGCCTCCCT | 55819 |
| rs762256238 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018292 | AGAGTGAGACTCCAT[C/T]TCAAAAAAAAAAAAA | 55819 |
| rs762282750 | snp | A/G | 8.27328e-05 | 0.00643114 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955621 | CTTTTTTCCTTCAAG[A/G]CAAAATCAGTCAGAA | 55819 |
| rs762286621 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984463 | TTAAAAATCAGGAAT[C/T]GATGTTGGACTTCGG | 55819 |
| rs762321279 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945286 | GGTGTGCTGACTGCA[C/T]CTGGGAAAACAGTGG | 55819 |
| rs762338593 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974616 | TGGACACGAGGGTGT[C/T]CAGGCCCATCTCCCT | 55819 |
| rs762339733 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044092 | CAGTTGTTTACACTT[C/G]AGCAATTTATTAAGT | 55819 |
| rs762342968 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936274 | ACAGGTAATTAAAAA[A/G]AATTTTTTGTAGAGA | 55819 |
| rs762397815 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964602 | CATGTGTGTTTCTCA[A/G]TCTGGGTTCCACAAA | 55819 |
| rs762402230 | in-del | -/TGAATTTTTAGGTTCAAGTTCT | 1.69467e-05 | 0.00291085 | frameshift-variant | RNF130 | GRCh38.p7 | 5:179970500 | CAGGATTTGTGGAAA[-/TGAATTTTTAGGTTCAAGTTCT]ACATGCCTATAAAAT | 55819 |
| rs762402946 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933683 | CGCTCCACCATGCCG[A/G]GCTAATTTTTTCTAC | 55819 |
| rs762416595 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989089 | GCCTCAGGAAACTTA[C/G]AATCATAGCAGAAGG | 55819 |
| rs762428410 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063054 | GAGGAAGGGGCTGGA[A/G]CTAGACCAGGTAGTG | 55819 |
| rs762437870 | in-del | -/AAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005436 | CTGTCTCAGAAAAAC[-/AAC]AACAACAACAACACC | 55819 |
| rs762483811 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061775 | CAGAGATCCTATTTC[C/T]AAATAAGGGCACATT | 55819 |
| rs762526127 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962287 | GCACTTCTTCCAAGT[A/G]TCTAGCCCCAGATGA | 55819 |
| rs762527455 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019042 | GTTATTCCTATATAA[C/T]CTATTATACGTAAAG | 55819 |
| rs762533079 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005126 | TGTATATCACTCCAC[C/T]GCTAAAAAACCGTAC | 55819 |
| rs762554894 | snp | A/G/T | 0.000140716 | 0.00838679 | missense | RNF130 | GRCh38.p7 | 5:180071669 | GGGCGAGCGCGGCGA[A/G/T]CCGGGCAGGGCCCGC | 55819 |
| rs762554911 | snp | A/T | 1.89921e-05 | 0.00308151 | intron-variant | RNF130 | GRCh38.p7 | 5:179970558 | ACCAAGAAACTTATT[A/T]GGCCAAAATGGAAAG | 55819 |
| rs762598609 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976138 | CGGCCTGGGCAACAT[A/G]GTGAGACCCCAACTC | 55819 |
| rs762607310 | snp | C/T | 1.65127e-05 | 0.00287334 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179978283 | AAAGTCTGGGTCAGT[C/T]TCCTAAAATGAAAAG | 55819 |
| rs762639672 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931033 | CCAAACCTCTGTCTC[-/AAAAAAAAAAAAA]AAAAAAAAAAAATCA | 55819 |
| rs762642961 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | RNF130 | GRCh38.p7 | 5:180040507 | TATTGTAGATGACTA[C/T]AGCAACTGCATTGTG | 55819 |
| rs762661350 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056008 | AGAATTGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 55819 |
| rs762687576 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020497 | TGAACCTCCTGCCAT[G/T]CGTCTGCTGGGAAGC | 55819 |
| rs762696221 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972374 | TATGCACTGGGTTAG[C/T]GCTAGGGTGGGGTGG | 55819 |
| rs762713103 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019955 | ACTGGAATAGTGGTT[-/C]ATGCAATCTGGGCAG | 55819 |
| rs762723021 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976910 | TTGGCAGGTGATTTC[C/G]TATTTATCCAATTGA | 55819 |
| rs762736878 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985994 | ATTTTTAAAGCCAAA[-/TC]TCTTTCTAAACTTTT | 55819 |
| rs762771686 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000815 | TCTACACGTTTTCTT[C/G]TATCTCTCTGAGTTT | 55819 |
| rs762788850 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043841 | AAAACATTCATATTG[A/G]TAGTACAATACAAAA | 55819 |
| rs762806213 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962964 | TTTTCTCTTCCTCCT[C/T]ACAGCTGTCCTAACA | 55819 |
| rs762807568 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948862 | TAAGACTGCCTTAAG[A/C]TGCTGGGTAGAATCA | 55819 |
| rs762834701 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928539 | TCCCATCAGGTTGTC[A/C]GTCTTCTTCTCCTTT | 55819 |
| rs762849113 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947675 | TTAATGCAGCAAAAT[G/T]CTTCAAAGAGGACCT | 55819 |
| rs762884057 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025462 | GGACAGTCTCATGTA[C/T]CTGCTGGTGAAGGCA | 55819 |
| rs762892386 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073750 | GGGTCCTCGCCCTGG[A/G]CCTGGCACCTAAAGA | 55819 |
| rs762939493 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988066 | CCTTTATAAATTTGA[C/T]AGGATTTGGCAGTAA | 55819 |
| rs762959223 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928469 | TTCATACATTTGCAG[A/G]CTGTTTGTGTATCTG | 55819 |
| rs762974209 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999920 | GTTGTTTTATATATC[C/T]TTTGTTATTTTTGTT | 55819 |
| rs763020546 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931949 | CCACTTCCCAGTTTT[C/G]CTTTGAGTCATCTTT | 55819 |
| rs763023630 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031451 | AAGATCACACCACTG[C/T]ACTCCAGCCTGGGTG | 55819 |
| rs763043409 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046293 | GGGGCTCCCACAGTG[C/T]AGTGGTGGGCTGAAG | 55819 |
| rs763055714 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012373 | GAGGGACCTAACACC[C/T]GGAACCTGGCACCTA | 55819 |
| rs763059077 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990803 | CCCCTTCAGCTACTA[C/T]CTCTGTATGGCCTGG | 55819 |
| rs763066836 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014371 | ATAAGCTGAAGCTGC[C/T]GGTGGCAACATGTAG | 55819 |
| rs763154168 | snp | C/T | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954942 | AAAGCAAAAGTATTT[C/T]ACCGGCACATGTAAA | 55819 |
| rs763199191 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035641 | ATGTCTGTTTCTCCT[C/T]CCCATTCTGTCAGTT | 55819 |
| rs763199461 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953383 | AAAGAAAACAAACCT[C/G]GAAAAGAACAAAGTT | 55819 |
| rs763209608 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064687 | TGAATCCCCATCCTG[C/T]GAGATGAATACACTG | 55819 |
| rs763264378 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990261 | GACTGATAAGGTCAC[A/G]TGAGTCACATGTCCA | 55819 |
| rs763293929 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058223 | CACTCAACTTCTCCA[C/G]TAGGTTCATGGCTAC | 55819 |
| rs763296622 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003176 | GTCAAGAAAGATTTA[A/G]CAGGTAAAACCGACA | 55819 |
| rs763353779 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974296 | TCCACGCGGCAACTC[C/T]ACTTCTGAAAACGTA | 55819 |
| rs763373727 | snp | A/G | 2.56157e-05 | 0.00357872 | intron-variant | RNF130 | GRCh38.p7 | 5:179963430 | ATGTGTTTTCCTGGG[A/G]TCATCTGGCACATGC | 55819 |
| rs763377880 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923497 | CACAGTGAACTGTCA[C/T]CTAAATGGATGTGTG | 55819 |
| rs763387969 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997270 | TCTCAGCCTCCTGAG[C/T]AGCTGGGATTACAGG | 55819 |
| rs763392031 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039449 | CAGCATGTCGGCCAG[A/G]GTGGTTTCAAACTCC | 55819 |
| rs763433465 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996001 | CTATTTCTGTGAATA[A/G]TATCACTGGCATTTT | 55819 |
| rs763441003 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957305 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGACAGA | 55819 |
| rs763510833 | in-del | -/AT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067606 | ACGGTATGTAAAAAC[-/AT]GTCATAAGCTGTAAA | 55819 |
| rs763514988 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940705 | TTTTTTTTCACTCTG[A/C]TTGGTGTTCCCAGTC | 55819 |
| rs763518319 | snp | C/T | 1.69648e-05 | 0.00291241 | intron-variant | RNF130 | GRCh38.p7 | 5:180013044 | ACGAACCAATCACTG[C/T]TGAGTACTGAGCTCA | 55819 |
| rs763552740 | in-del | -/ACAGT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975748 | AAAGACAACCAAGTA[-/ACAGT]ACCATAGAGGGTGCA | 55819 |
| rs763564499 | in-del | -/CTGTGT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977947 | CTCAACACTCCTAGG[-/CTGTGT]CTGGGGAGTCTGGAG | 55819 |
| rs763582582 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051029 | GCTGGTCTCGAACTC[C/T]TGAACTCAAACAATC | 55819 |
| rs763599600 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012473 | CTCACACCGGGGAAG[C/T]ACACTGCTTTTCCTA | 55819 |
| rs763616345 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999866 | AAGGTTATTACTGGT[A/G]GGTGAGGACTTATTC | 55819 |
| rs763630228 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967816 | TGGGCAAAAGAACTG[C/T]TTCAGGTCATCTCAA | 55819 |
| rs763635266 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005213 | CGGGTGGATCACCTA[C/T]GGTCAGGAGTTTGAA | 55819 |
| rs763635777 | in-del | -/GAGTTTCCCACTAAGTAGCCTGTAGCCCCGGAGGTGGAGAGCACGA | 1.70443e-05 | 0.00291923 | frameshift-variant | RNF130 | GRCh38.p7 | 5:179970504 | ATTTGTGGAAAACAT[lengthTooLong]GCCTATAAAATAATG | 55819 |
| rs763695545 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956630 | TCGCTGATCCTGCTC[A/T]GTGCGGTCCTCACTG | 55819 |
| rs763713023 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001853 | TTCTTGAAGACTAGT[A/G]CAGGTTCAAGCAAGC | 55819 |
| rs763714758 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006514 | AGTCAAAGAATATTA[C/T]ATACACATGTTATGG | 55819 |
| rs763746323 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022623 | ACACATCAATGTACA[C/T]GGAGCTCACGTGACT | 55819 |
| rs763805953 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957395 | CCAGCCTGGGTGAGA[C/G]AGCGAGACCCTGTCT | 55819 |
| rs763814706 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068533 | TACTACGTAAAGTAT[A/G]GCACTTGCCAAAATA | 55819 |
| rs763840931 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922567 | ATCTGCATCAGCCTC[C/T]CAAAGTGCTGGGATT | 55819 |
| rs763867805 | in-del | -/CTGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019189 | AAGATCAAAACCATC[-/CTGA]CTGACTAACACGGTG | 55819 |
| rs763876290 | snp | A/G | 3.30535e-05 | 0.00406518 | intron-variant | RNF130 | GRCh38.p7 | 5:179967015 | GGCAAATTCGGCTGC[A/G]AAATATTTCCAGGTT | 55819 |
| rs763878817 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017767 | AAATCAGTTTTGAGA[G/T]GCCAACAGAAGGAAC | 55819 |
| rs763892600 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968668 | GAGACTCTGTCTCAT[A/T]AAAAAAAAAAAAAAA | 55819 |
| rs763911713 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010552 | TTTTAGTGGAGATGG[G/T]GTTTGCCATGTTGGC | 55819 |
| rs763911789 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999459 | GGCCATGGTGGCTTA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs763932639 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986689 | TTTACATTTCTTCCA[A/G]CTGTGAATGGTGCCA | 55819 |
| rs763940700 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021107 | AGTAGCTGCAATGTC[A/C]GACACGTACCACCAA | 55819 |
| rs763974837 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988093 | GTAAAGCCATCTGGT[C/T]CTGAGTTTTTGTTGA | 55819 |
| rs763974960 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061991 | TGTCTGCTTCATCAA[C/T]GGAGACTTCTTTGTG | 55819 |
| rs763988002 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967842 | CTCAAAGCCTTATTT[A/G]AAACAGCAAAAGGCA | 55819 |
| rs764008605 | snp | A/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072989 | AAGATACACATCGCT[A/T]TAAAGTATCAGCTAA | 55819 |
| rs764010029 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950125 | TAAATAACTTTTTTT[C/T]TTCTTGAGATAGAGT | 55819 |
| rs764016262 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934917 | ATCTTTATTTCCTTC[C/T]TTTGATTTAGTTTGT | 55819 |
| rs764017044 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928556 | TCTTCTTCTCCTTTA[C/T]TGTGACTGTGAGTCC | 55819 |
| rs764027868 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990297 | CAGGGGGCCCTTCCC[C/T]GTTAGGTAGCCGAGG | 55819 |
| rs764030048 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967332 | CAAACATCCAGTTTA[A/C]AAGAGTAAACTATTA | 55819 |
| rs764040196 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965429 | TGCTAAAGGTGATTA[A/G]TTTGGTATATGAAGT | 55819 |
| rs764064209 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032475 | CTCCTGGGCTCAAGT[A/G]ATTCTACCACTTTAG | 55819 |
| rs764083161 | snp | A/G | 4.76508e-05 | 0.00488089 | missense | RNF130 | GRCh38.p7 | 5:180071600 | TGATGAGCGCCGTGT[A/G]GTACTCCTGGCTCGC | 55819 |
| rs764135483 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986437 | CCATGGTGTAATATT[C/T]AAGATTCATGATACT | 55819 |
| rs764164998 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013510 | TGTTGTGTGGTACTT[-/A]AAGACTTAAACAGAC | 55819 |
| rs764224792 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064692 | CCCCATCCTGTGAGA[C/T]GAATACACTGACTCC | 55819 |
| rs764229475 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952043 | TAAAATAATAAAGAT[C/T]TGAGTAAGGCCAGGT | 55819 |
| rs764239344 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022608 | TTTGGAAGCCACGGC[A/C]CACATCAATGTACAC | 55819 |
| rs764251766 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971526 | AGCAGCCCGCCACCA[A/C]GCCCAGCCAATTTTT | 55819 |
| rs764269484 | snp | A/G | 2.30248e-05 | 0.00339291 | intron-variant | RNF130 | GRCh38.p7 | 5:179966800 | TGAGCGGAGGCCCCC[A/G]CTTACTTGTTACTGC | 55819 |
| rs764277030 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948386 | TTCTGTTTGTTGCTC[A/T]TGGCCTGGTGCATTG | 55819 |
| rs764292393 | snp | A/T | 1.6612e-05 | 0.00288196 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015257 | GCTTTAAATTTCCCT[A/T]TAGAAATCTCTTAAA | 55819 |
| rs764293991 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978129 | CTCAAAAGCAAGGGA[A/G]ATGCCCACCCTGAAA | 55819 |
| rs764320429 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944115 | TAGCTGGGACTACAG[A/G]TGCCTGCCACCATGC | 55819 |
| rs764360354 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052804 | AAAAAGAAAGACTGA[C/G]AGAGATTGCTCACCT | 55819 |
| rs764386285 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026751 | TAAATGAAAAGAAAG[C/T]TTAACAACCAAACTA | 55819 |
| rs764387173 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054012 | AGCAGAGATGGGGTT[G/T]CACTATGTTGGCCAG | 55819 |
| rs764409393 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939478 | CGATGACTTTGCATG[C/G]AAGCGCAGCAGCTGC | 55819 |
| rs764423739 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953433 | ATTTCAAAACTTACT[A/G]TGAAACCAATGGAAG | 55819 |
| rs764426930 | snp | C/T | 1.6566e-05 | 0.00287797 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015308 | ATCTGTGGTATAAGA[C/T]ACCAGGTATGGCTAT | 55819 |
| rs764440371 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051889 | GCAACAGATACTTCA[G/T]GCAAGATGCTACAGA | 55819 |
| rs764468400 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981691 | TAACAAAAGTAACAA[C/T]GATTAATCAACATTA | 55819 |
| rs764487906 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027914 | CCCCAGTGCAGCGCT[C/G]GAAAGCACAGCTTAG | 55819 |
| rs764494440 | snp | A/T | 1.65051e-05 | 0.00287267 | intron-variant | RNF130 | GRCh38.p7 | 5:179978163 | AGGCATACAAAGCAC[A/T]TTAATATCATTCTTT | 55819 |
| rs764516949 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930182 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 55819 |
| rs764530194 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933570 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTGCA | 55819 |
| rs764560037 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974594 | CTTGTGAATCGTTAA[C/G]GAAAGATGGACACGA | 55819 |
| rs764585149 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930466 | ATATTGAATTTTCTA[C/T]ATGTAATCGTTTTCT | 55819 |
| rs764593438 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995203 | GTATGGGACCTGCCT[-/CT]CTCTCTCTCTCTCCA | 55819 |
| rs764622157 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069545 | CACACTGCCCAAATG[C/T]GTTCATTTTGTTGCA | 55819 |
| rs764626585 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046010 | GGAGCAGGGGGCAGC[A/G]CTCGCCGGGGAGGCT | 55819 |
| rs764648968 | snp | A/C | 0.000153504 | 0.00875947 | missense | RNF130 | GRCh38.p7 | 5:180071675 | GCGCGGCGAGCCGGG[A/C]AGGGCCCGCCCGCCC | 55819 |
| rs764651353 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930441 | CATTTTAAGAGCTGA[C/T]TTGTAGAATATATTG | 55819 |
| rs764670955 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944931 | CTCACACGTGGCAAA[A/G]CTTTATTTTATCACT | 55819 |
| rs764678629 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058152 | TTACTGCTGGGGAGC[A/G]AGGAGGGAAGGAGCC | 55819 |
| rs764693958 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960079 | TATTTATTTTTCTTA[C/T]TTTGAGGGAAAACTA | 55819 |
| rs764720038 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920781 | GGGCATATATATTTA[-/TA]TATATATATATATAT | 55819 |
| rs764752961 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001345 | ATTCCAGGAGCAGGT[A/G]CTCAGAATGACAATG | 55819 |
| rs764753392 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049173 | GACAAAACCCAAAAA[C/G]AAAGCTTCTTTGGTT | 55819 |
| rs764767785 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967716 | GGCAGCACATGAGAA[A/G]CACAGCTGGGAGGGG | 55819 |
| rs764770593 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017466 | TCCCCAAAAACCTTT[C/T]ACTCAATGCTCTCAG | 55819 |
| rs764796576 | snp | A/G | 3.33873e-05 | 0.00408565 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179970485 | AAGCCAGGGATCCAC[A/G]CAGGATTTGTGGAAA | 55819 |
| rs764865315 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986451 | TCAAGATTCATGATA[A/C]TGCACTAAACACATT | 55819 |
| rs764868932 | snp | C/T | 2.84531e-05 | 0.00377171 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071577 | GCCGGGCTCCTGCAC[C/T]GTCACGTTGATGAGC | 55819 |
| rs764914928 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009435 | AGAAAATGGGCAAAA[G/T]ACATGAATGGATATT | 55819 |
| rs764948350 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934718 | CGGCTACTTTATTTT[C/T]ATTCTTGTAGAGATT | 55819 |
| rs764952123 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048089 | TTTTCATTTTTACTT[C/G]TATGAACCCAGTTTC | 55819 |
| rs764957587 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062112 | CAGGCTGGAGTGCAG[C/T]GGCACGACCTTGGCT | 55819 |
| rs764970986 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921110 | TAAAACTGTTTTTAA[G/T]CTTTACTGGGGTATA | 55819 |
| rs764991650 | snp | C/T | 1.86021e-05 | 0.0030497 | intron-variant | RNF130 | GRCh38.p7 | 5:179970553 | TACATACCAAGAAAC[C/T]TATTAGGCCAAAATG | 55819 |
| rs765043589 | snp | C/T | 1.84245e-05 | 0.00303511 | missense | RNF130 | GRCh38.p7 | 5:179966820 | CTTGTTACTGCAATG[C/T]TGATTTCTCCTGTTC | 55819 |
| rs765054217 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947763 | AAAAGTATATGTGTG[C/T]ATATGTAAGTATATA | 55819 |
| rs765098326 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947461 | CCCCACAGCCTGCCC[-/CT]GACACTTGGTGAGCT | 55819 |
| rs765099775 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979301 | AAGTTCACTAAGAAT[A/G]TCTCCACCCTCTGAA | 55819 |
| rs765113450 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048711 | AATTCAGCACCTCAG[C/T]AGTGTCACCAGGATC | 55819 |
| rs765127695 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961995 | ATGGTCCTAGCATTA[C/T]CTGTTTATGAATGAC | 55819 |
| rs765143785 | snp | A/T | 1.64822e-05 | 0.00287068 | missense | RNF130 | GRCh38.p7 | 5:180013241 | TTGTACAGAGATGTT[A/T]TTCTCCAGATAACTC | 55819 |
| rs765153386 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945240 | CTTTCCCTCCACTAC[A/G]ATGAGCAAGGCTCAG | 55819 |
| rs765176112 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941021 | CTTTCAATTATTTTT[C/T]AGTCCTCGCATTTCC | 55819 |
| rs765201757 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926288 | GGGCCACTGTTAAAA[C/T]TTTCTTTTGAATTTT | 55819 |
| rs765202918 | snp | A/C | 4.97682e-05 | 0.00498815 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015281 | TCTTAAAATGTTGTT[A/C]AACGGGCCATGATCT | 55819 |
| rs765204751 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969420 | ATAAGCAATGACATC[A/G]TTTTATATTATGCCA | 55819 |
| rs765209643 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001126 | TCTCTGTGCAGTTTC[A/G]GCTGAATTCAACATC | 55819 |
| rs765237435 | in-del | -/GA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981303 | CCCAGGCACATCAGG[-/GA]GAGACGTCACTCTAG | 55819 |
| rs765244014 | in-del | -/T/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029867 | TTTTTTTTTTTTTTG[-/T/TG]AGACAAGGTCTTGCT | 55819 |
| rs765323344 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973101 | CCATCCACCCCATCC[-/CT]CTCTTACTCCTGACC | 55819 |
| rs765330019 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952806 | ATTTCATGATAAAAA[C/T]GTTCAATAAGCTAGA | 55819 |
| rs765338202 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044868 | CCACATTCACTGAGG[C/G]ATCATAATTGGCACC | 55819 |
| rs765352255 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930107 | TTGTCGCCCAGGCTA[C/G]AGTGCAATGGCGTGA | 55819 |
| rs765364130 | snp | C/T | 5.11352e-05 | 0.00505618 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071688 | GGCAGGGCCCGCCCG[C/T]CCCGCGCAGCTCATC | 55819 |
| rs765368207 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963364 | ATCCCATCAGGATCC[A/G]TATGAAACTGGTAGA | 55819 |
| rs765385081 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974963 | GTGAAGCGGTCCTCT[A/G]AGAGTGAAGAACAAG | 55819 |
| rs765385195 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950892 | AGGAGAGAAGGAAAG[-/A]AAAAAGGAAGAATTG | 55819 |
| rs765397899 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030411 | CAAGACTCATCTTTG[C/T]AAGTGTACAATGAGT | 55819 |
| rs765419183 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989431 | CTTATTTATGGGTGC[C/T]ATGGTGTTGGGTGTA | 55819 |
| rs765422108 | in-del | -/GT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935517 | GATATGTCAGCACGT[-/GT]GTGTGTGTGTGTGTG | 55819 |
| rs765437304 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012233 | AAGGATAAAAATCCC[A/C]GTGTGCCCATCCCCA | 55819 |
| rs765464153 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980712 | CAGCTCCACTTCTGG[C/T]TCGCTATACTATCAT | 55819 |
| rs765470488 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956038 | CTTTAAAAAATGCTC[A/C]TCTTACCTCTCAAAC | 55819 |
| rs765515084 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057050 | AGAGGAGCATGTTTT[C/T]TTATTCAAAATAAGC | 55819 |
| rs765530290 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063387 | CAAGGATGGTCCTAA[C/T]TTGTGTAAATAACAA | 55819 |
| rs765534707 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994545 | TAATTTGAGTAGGAT[C/T]GTTTGACTTTGCTTC | 55819 |
| rs765547987 | snp | A/G | 0.000148887 | 0.00862678 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955636 | GCAAAATCAGTCAGA[A/G]AGCAGGTTTTTTCTT | 55819 |
| rs765552378 | in-del | -/ACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061280 | CTTTTGGAAAAAACC[-/ACA]ACAACTGACGTGACT | 55819 |
| rs765571054 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950443 | ATTTTGATACTAATC[A/G]TATTTCTGGTTTTAG | 55819 |
| rs765571303 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964521 | ATTACCTATATATGT[C/G]CAAGAAGGCAGAGAG | 55819 |
| rs765574528 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067295 | TTTTAAAGCTATATA[A/G]CCCATCATTGTACAC | 55819 |
| rs765579925 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973813 | GGGTGGGTGGTGCAT[C/T]GGGACGGAAAGCAGG | 55819 |
| rs765588088 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992072 | GTCACTCACCTGATG[C/T]TCAGCTCCTGCTGTG | 55819 |
| rs765633886 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039371 | CAGCCTCAGTAGCTG[A/G]GATTACAGGTACCCT | 55819 |
| rs765732693 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950927 | ATCTCCACTGAGATG[-/A]AAACCAGGTGGGGAG | 55819 |
| rs765751039 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983724 | TGTATACATCCACTT[-/G]GGGGAGAACTGGCAT | 55819 |
| rs765756596 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973818 | GGTGGTGCATCGGGA[C/T]GGAAAGCAGGTAACG | 55819 |
| rs765766034 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924495 | GCAAAACTCTGTCTG[-/A]AAAAAAAAAAAATAA | 55819 |
| rs765766630 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | RNF130 | GRCh38.p7 | 5:179980191 | TCTTGGCTGCATCTC[C/T]GAGACGACGCTATGA | 55819 |
| rs765770184 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933948 | ATTTTTTCTAGATCT[C/T]TGAGCTGCACCTCCA | 55819 |
| rs765787103 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956903 | CTTGGGAAACAGCAT[C/T]TCAATGAATGAGGGG | 55819 |
| rs765834510 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934131 | AATAAGAACCTGGTG[C/T]TTGCCTCTCCTTTAG | 55819 |
| rs765844491 | in-del | -/AG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060047 | GAGAAAGTCAAAGTC[-/AG]AGACTTGAAGATGGG | 55819 |
| rs765853991 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933528 | TTTTTAATTTAAAAC[-/T]TTTTTTTTTTTTGAG | 55819 |
| rs765872376 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030322 | TTAAGAATCTTGTAT[C/T]TGTGTTGCTTTTGAA | 55819 |
| rs765898107 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060297 | GCAATAAGAAACTAA[C/T]ACACCAAGGCTAAGC | 55819 |
| rs765903603 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937718 | TAACCCAAAGAATTG[A/G]AAACAAGGATGCAAA | 55819 |
| rs765930750 | snp | A/G | 1.65765e-05 | 0.00287888 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015286 | AAATGTTGTTCAACG[A/G]GCCATGATCTGTGGT | 55819 |
| rs765950164 | snp | C/T | 1.65556e-05 | 0.00287707 | intron-variant | RNF130 | GRCh38.p7 | 5:179978292 | GTCAGTTTCCTAAAA[C/T]GAAAAGTACAGAAAC | 55819 |
| rs765954457 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962310 | CCAGATGAGGTTAGA[C/T]TGAATAACACATGCC | 55819 |
| rs765959552 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042384 | ACGACCATTACCTAC[C/G]CTTTTCCTTAAAAGG | 55819 |
| rs765969597 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180071082 | AAGTCCGTGATTTGA[A/G]GAACCTGCCGCTTCC | 55819 |
| rs765973450 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065368 | TAACACAATCGTAGT[A/T]CACAATGTTCCCGTT | 55819 |
| rs765997101 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965766 | GAATGAAGCCTCCCT[A/G]AGTTTACACAGATGA | 55819 |
| rs766042748 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019044 | TATTCCTATATAACC[A/T]ATTATACGTAAAGCA | 55819 |
| rs766058069 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059555 | TTTAGGATTTTTCTG[A/G]TCCAGATGAATTAGT | 55819 |
| rs766060328 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947397 | CCAGCACACTTCCTG[A/G]CCTTTTCTACTATCA | 55819 |
| rs766080581 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042089 | TGTAGTAGATAAAGA[G/T]ATGACGCCAGTGGGA | 55819 |
| rs766116297 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932902 | ATTTTCTTTCTTGTA[A/T]TGCCCTTGTAATAAT | 55819 |
| rs766125266 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974712 | GCGATGGCTTTGAAA[C/G]AGAGTTTTAAAAACT | 55819 |
| rs766183803 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977360 | GAGCTCGATGGAAGT[C/G]TCACTGAAGGGCTTG | 55819 |
| rs766184302 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041173 | CAACCATGTTAGAGC[A/G]AATTTCTTCATAAAT | 55819 |
| rs766202999 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986374 | GTCATGACTTCTCTC[C/T]GCTTCTTGGGAGCAT | 55819 |
| rs766210230 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981527 | CGGCTTCCATTACCA[C/G]TACTTTACTTCTATT | 55819 |
| rs766222130 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020864 | CAGTGAAGAATTTCC[A/G]GGGGTTGCCAACTTT | 55819 |
| rs766223247 | snp | A/G | 0.000170867 | 0.00924145 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015400 | ACACCAGGTACAAAC[A/G]GTTTTAGAAATCAGT | 55819 |
| rs766239602 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052624 | ACTGGGCTATCTGGA[A/C]CATAATTTAAAATGT | 55819 |
| rs766246337 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004084 | CCACATCAAAGGCTA[A/G]TAAGTAGGCCCTATC | 55819 |
| rs766275883 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971246 | CAAGCTCTAGCACCC[A/G]GCCCAGCAGCCTTCT | 55819 |
| rs766278288 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | RNF130 | GRCh38.p7 | 5:179966902 | GTGGCTCAAGGCCAA[A/G]GGAGTTGTCGCCGGC | 55819 |
| rs766282558 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008201 | ACCCCAGAAAAAGCC[A/G]AGAAAAGCCCAACTC | 55819 |
| rs766295807 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054016 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGATG | 55819 |
| rs766297015 | snp | C/T | | | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179919925 | TCTCCCACAGGGCAG[C/T]ATGCATCGTAAGCAG | 55819 |
| rs766338547 | snp | A/G | 1.67545e-05 | 0.0028943 | missense | RNF130 | GRCh38.p7 | 5:179966841 | TCTCCTGTTCTCGGA[A/G]TGAGCTCCCCATCCT | 55819 |
| rs766364411 | in-del | -/GCATGTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947890 | ACACAGACCATATAT[-/GCATGTA]AGAATATGGGTGTGT | 55819 |
| rs766365784 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970349 | GCCAATTATGTTATA[C/T]TGTATTACACATACA | 55819 |
| rs766394988 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025334 | ATATGATTTTACCTT[C/T]CTCCTCTTCTGCTGC | 55819 |
| rs766402268 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957858 | CAAAAGGTTATCAGG[-/T]TGAGAACTAAAAATT | 55819 |
| rs766480813 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928668 | GAGTCTCGCTCTATC[A/T]CCCAGGCTGGAGTGC | 55819 |
| rs766483951 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996450 | AGTATGATGTTGGTT[G/T]TGGGTAAGTCATATA | 55819 |
| rs766492906 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943059 | AATTAGTTGGGCGTG[C/G]TGGCACGTGCCTGTA | 55819 |
| rs766502415 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972885 | AACTGTTTCCTTCTA[A/G]GATTATTGATATAAA | 55819 |
| rs766506422 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009513 | TAATTAGAGAAATGC[A/T]AACTAAAACCACAAG | 55819 |
| rs766509458 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068108 | GCCGATACTAAACTC[C/T]TCCCCACCAGCACAT | 55819 |
| rs766511282 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056154 | TTTGGAAAAGAAAGT[A/C]AAAAAACTAGAAAAT | 55819 |
| rs766553210 | snp | A/C/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955100 | ATTGAGCACTTACGA[A/C/T]GTGCAAAGCACTCTG | 55819 |
| rs766562016 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968067 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 55819 |
| rs766563477 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929993 | TACATATATTCCTCA[C/G]TATGATGTTTCTTTG | 55819 |
| rs766568750 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038408 | AAAAAAAAAGCCTGT[-/T]TTGTTTTTTTTTTTA | 55819 |
| rs766570986 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962384 | ATTACAGTTTCTATA[C/G]CCAGACAATGGGCAG | 55819 |
| rs766581828 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044734 | CTACTCAGAAGGCTG[A/C]GGCAGGAGAATTGCT | 55819 |
| rs766590244 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980548 | TTCTTGCACACTCCA[C/G]AGCCACTCCTGCTGC | 55819 |
| rs766592475 | snp | A/G | 1.69504e-05 | 0.00291117 | intron-variant | RNF130 | GRCh38.p7 | 5:180013046 | GAACCAATCACTGTT[A/G]AGTACTGAGCTCACC | 55819 |
| rs766605189 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034111 | TTTTTTTTTTAAATC[A/G]TGATGGGTACTGAGA | 55819 |
| rs766616291 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966572 | ACTAAGACAGACCTC[C/T]GAACAGCTACTCATC | 55819 |
| rs766632230 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991021 | GCTTGTTGCCCACAT[C/T]TGCTTGTCTGAGAAA | 55819 |
| rs766634620 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953227 | TCCCATGCTCATGAG[G/T]TGGAAGACAATATTG | 55819 |
| rs766648287 | in-del | -/TCTCAGCC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029960 | TCAAGGATTCTCCTG[-/TCTCAGCC]TCTCAGCCTCCCAAG | 55819 |
| rs766685643 | in-del | -/GGATTGTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994541 | GATGTAATTTGAGTA[-/GGATTGTT]TGACTTTGCTTCTGA | 55819 |
| rs766745294 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004087 | CATCAAAGGCTAGTA[A/C]GTAGGCCCTATCCAG | 55819 |
| rs766746472 | snp | A/G | 0.00343052 | 0.0412734 | missense | RNF130 | GRCh38.p7 | 5:180071476 | TGGAGGGGCAGCGGC[A/G]CCAGCACCTGGCCGC | 55819 |
| rs766766513 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973749 | AAAAGAAGTTCCCCA[C/G]TCACGTGATAAAAAC | 55819 |
| rs766799533 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058247 | TGGCTACATCAGTGT[A/G]TTCATTCTGTGGGAA | 55819 |
| rs766812016 | in-del | -/TCATA | 1.67409e-05 | 0.00289312 | intron-variant | RNF130 | GRCh38.p7 | 5:179967060 | GGAAAACACAACCTT[-/TCATA]AGATTCTAAAAAAGA | 55819 |
| rs766822576 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180010245 | GTGAGACTACATCTC[-/A]AAAAAAAAAAAAAAA | 55819 |
| rs766838898 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037046 | ATGATATCCAACTAT[A/G]AATATTCTTCTATAA | 55819 |
| rs766846545 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066954 | CAATCACTCAACTCC[C/T]CGAGGTCAAGGCTAC | 55819 |
| rs766855885 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973918 | CTTGGGGATACAGAA[C/T]GAGAAACAAATAGAA | 55819 |
| rs766889721 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047917 | TCCAGTCGAACCTTC[A/T]ATACTGACGCTCCCG | 55819 |
| rs766923248 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967544 | TATAAGAAAATGATC[C/T]GTTTCAAAACCTAAG | 55819 |
| rs766924548 | snp | C/T | 1.65452e-05 | 0.00287616 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955651 | AAGCAGGTTTTTTCT[C/T]CTTCAAAACCATTCT | 55819 |
| rs766928792 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037895 | ATGCACACCTCCACT[C/G]TTTGCCTTACCTTCC | 55819 |
| rs766996362 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996201 | TTCCTATGTATTTTA[C/T]TCTTTTTTGGTGGCT | 55819 |
| rs766998465 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020756 | GCAAGCACCTGCCCA[A/G]AACAGAAAGCTTTCT | 55819 |
| rs766999916 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041069 | CACCACCGCTATCCC[C/T]ACAGTGAGAAAACAG | 55819 |
| rs767033432 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996230 | CTATTGTAAATAAGA[C/T]GGACTTCTTGATTTA | 55819 |
| rs767042766 | in-del | -/TTTGT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986709 | GAATGGTGCCATGTA[-/TTTGT]TTTAATAATTTTTAA | 55819 |
| rs767046959 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941598 | TCTAGTCACTGCTTA[C/T]GAACTGGCAGATGCC | 55819 |
| rs767053120 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923742 | GTTGCTTTGAACCTA[C/T]TTCGGTCCTGGGGGC | 55819 |
| rs767087800 | in-del | -/AT | 1.64784e-05 | 0.00287035 | intron-variant | RNF130 | GRCh38.p7 | 5:179980240 | GATACTAAGTGTAAG[-/AT]CTCTGAATGACGTAC | 55819 |
| rs767092941 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052478 | CTTGATCCAGAGCAG[C/T]GCCTGAAGGCACTAC | 55819 |
| rs767100155 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938292 | ACATTATGGTAAGTG[A/G]AAGAGGCCAAACACA | 55819 |
| rs767147429 | snp | A/G | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:180040525 | CAACTGCATTGTGGA[A/G]AGCGGCCCGTGATAT | 55819 |
| rs767194554 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998108 | CCTCCCAAAGTGCTG[C/T]GATTAGAGGCGTGAG | 55819 |
| rs767200191 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060690 | ATCTCTACATAAATA[-/G]CGTAGTCTTCTGGAG | 55819 |
| rs767213918 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034308 | GAATTTTTGTGCCTA[C/T]ATTCGTAAGGGATAT | 55819 |
| rs767270269 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945328 | CCCAAACGCTGCACA[A/G]ATCAGCTGCAAAACC | 55819 |
| rs767297137 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950328 | TGCCATGTTGGTCAG[C/G]CTGGTATCAAATCCC | 55819 |
| rs767304443 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000900 | ATTGGAGTGTGTTAC[C/T]AGGGAATTACGTTCC | 55819 |
| rs767319418 | snp | C/T | 8.13129e-05 | 0.00637572 | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015426 | TCAGTTGAGGCTCCC[C/T]CTTGAAGACTCAAGC | 55819 |
| rs767329139 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179988251 | TCACAAACCTCTAAT[A/G]ATCCTTTGTATTTTG | 55819 |
| rs767336489 | in-del | -/GGCTGGAATGCAACG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949010 | TCGCTCTGTCACCCA[-/GGCTGGAATGCAACG]GTACCATCTCAGCTC | 55819 |
| rs767413765 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044733 | GCTACTCAGAAGGCT[C/G]AGGCAGGAGAATTGC | 55819 |
| rs767417202 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180019517 | AGACTGCTGGCTCCT[A/G]ATCCCAAGACTTCTC | 55819 |
| rs767422695 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065657 | CCCAGCTACTCAGGA[C/G]GCTGAAGCAGGAGAA | 55819 |
| rs767425125 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922712 | GGAGGCTGAGCCAGA[C/T]GGCTTCAGCTCAGGA | 55819 |
| rs767426796 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938104 | TGGGACTACAGGTAC[A/G]CGGCACCACGTCTGG | 55819 |
| rs767450548 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006122 | TTCTCAGCTCAAACA[C/T]CTATTTCCCCTTTCC | 55819 |
| rs767491869 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023439 | GTGTCATTACTGATA[A/T]AGTTCAATAATGCTC | 55819 |
| rs767493874 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971354 | TAATCTGAGTTTGGG[A/T]TAAGATAAAAGAAAT | 55819 |
| rs767509134 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005460 | CAACACCAACAGAAA[C/G]CATATTGATTATAGA | 55819 |
| rs767558093 | snp | A/T | 1.65026e-05 | 0.00287246 | missense | RNF130 | GRCh38.p7 | 5:179967004 | TATCAGTACATGGCA[A/T]ATTCGGCTGCAAAAT | 55819 |
| rs767561232 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066102 | CTCTGATATGGTTTG[A/G]CTCTGTGTCCCCACC | 55819 |
| rs767574503 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031543 | GTAGCTTTTTGACTG[C/T]GTGGGGGTCAGTGTC | 55819 |
| rs767604776 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022676 | TCTCCATTTGAACTG[G/T]TACTTAAGCCACGTC | 55819 |
| rs767644181 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979476 | TTGGGTGTGGGGCAG[A/G]AGACAGTTTTCGTTT | 55819 |
| rs767658385 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991772 | ATTATTAAATTGTAA[C/T]ATATAATGAAATAAT | 55819 |
| rs767670454 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009467 | CACTGAAGAGGATAT[A/T]CGGATGGCAAACAAG | 55819 |
| rs767686146 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958410 | GAAGATGGTTTTTAG[-/A]AAGTCTGAAAAACAC | 55819 |
| rs767727843 | snp | G/T | 2.44412e-05 | 0.00349571 | intron-variant | RNF130 | GRCh38.p7 | 5:179963443 | GGATCATCTGGCACA[G/T]GCAATCCAAAAACAA | 55819 |
| rs767756996 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972438 | GTGGACGATGGGACT[C/T]GGCTGACTGACAGGT | 55819 |
| rs767794439 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984473 | GGAATCGATGTTGGA[C/T]TTCGGCAAATATCTT | 55819 |
| rs767797824 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066802 | CGCGCCATTGCACTC[C/T]GCCTGGGCAACAAGA | 55819 |
| rs767816686 | snp | C/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955292 | CCAGCAGGATGTCCC[C/T]GCTCTTGCGCCCTAT | 55819 |
| rs767818842 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930776 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs767836647 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926963 | CCCCCTCGCCCCACT[C/T]GACACTGCCCCCACC | 55819 |
| rs767880992 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060075 | TGGGGGAAGGGGCCA[C/T]GGGCCAGGGAACACA | 55819 |
| rs767891350 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974322 | ACGTACTTCTAACGA[C/T]TACACACTCCGATGG | 55819 |
| rs767892695 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014714 | AACAGGGCTGGGCGT[C/G]GTGGCTCATGCCTAT | 55819 |
| rs767901987 | snp | C/T | 1.65471e-05 | 0.00287633 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955653 | GCAGGTTTTTTCTTC[C/T]TCAAAACCATTCTAC | 55819 |
| rs767916404 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980403 | AAAAGTGTTAGAACA[C/T]CCTGTTAGGTCAAAC | 55819 |
| rs767928213 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037931 | CTAAATATATCCTCA[A/G]ACTATACCCCTGCAT | 55819 |
| rs767977599 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966444 | AGAGCACGAGCGCTC[A/C]CAGCATACAACACAC | 55819 |
| rs767980214 | in-del | -/ATTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978873 | GTATTCAGACACCAG[-/ATTA]ATTGATTTCCTTCCT | 55819 |
| rs767999729 | snp | A/C/G | 0.000180983 | 0.00951131 | missense | RNF130 | GRCh38.p7 | 5:180071527 | TCAAGCCCGTAGCGC[A/C/G]CGCGGTCGATGCGAA | 55819 |
| rs768000683 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035780 | TTTTGAATCTGCTGT[C/T]GAAGGCCTCTAGTGA | 55819 |
| rs768013494 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990024 | GTTTGCTTGTAGGGT[A/C]CAGCCCCACGGGGTT | 55819 |
| rs768017719 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949298 | AAGACAAGGTCTTGC[A/T]GTGATGCCCAGGCTG | 55819 |
| rs768023439 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953575 | ACTGAATATCCACAT[A/G]CAAAAGAATGAAGGT | 55819 |
| rs768067326 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965695 | TAAACGAATCGAGAG[A/G]TGGTGAGAAATGAGC | 55819 |
| rs768070858 | snp | A/G | 3.50085e-05 | 0.00418366 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071559 | CGTGAGCGGGGCGCC[A/G]CGGCCGGGCTCCTGC | 55819 |
| rs768088483 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977653 | AGGTCAGGAGTTCAA[A/G]ACCAACTGGCCAACA | 55819 |
| rs768143661 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975588 | TGCTGAGCAGGCTGT[A/G]TGGTGCAGTCTCAGG | 55819 |
| rs768144963 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064003 | CACTGTGCCCAATTC[C/T]ATTACCGCTGAGAGC | 55819 |
| rs768156520 | in-del | -/GGAAAGGAGTAGGGAAAGGAGTAG | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015654 | GTAGGGAAAGGAGTA[-/GGAAAGGAGTAGGGAAAGGAGTAG]GGAAAGGAGTAGGAA | 55819 |
| rs768200524 | in-del | -/CC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004266 | TCCCGTAATACGCTA[-/CC]CACTCACTGATATTC | 55819 |
| rs768233635 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989148 | AATGAGTGCCAGCAG[G/T]AGAAACGCCAGACGC | 55819 |
| rs768248805 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977809 | GTGAGCCGAGATTGC[A/G]CCACTGCACACTCCA | 55819 |
| rs768261221 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052472 | ACCACCCTTGATCCA[C/G]AGCAGCGCCTGAAGG | 55819 |
| rs768287128 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971087 | CAGCTGAAATGTTAA[C/T]GGGGGAGGATGGGAG | 55819 |
| rs768308496 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051091 | TACAGGCGTAAGCCA[C/G]CAAACCTGGCCAATT | 55819 |
| rs768322259 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968619 | TGCAGTGAGCTGAGA[C/T]CACACCACTGCACTC | 55819 |
| rs768323644 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978622 | TGCATTACTTATTGG[C/T]CTGAAGAGGTTTCAC | 55819 |
| rs768337749 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179993674 | CTCCCATTCTGTAGG[C/T]TGCCTGTTCACTCTA | 55819 |
| rs768388739 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969565 | ATCGACCAACAGAAG[C/T]ACCCTTTTAAAAGTG | 55819 |
| rs768476295 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069071 | TCATTTTCTTAACAC[A/G]AATAATTTTAACAGA | 55819 |
| rs768531511 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982183 | GCTTCTTTGACTCAG[C/T]ATGATTATCTTGAGA | 55819 |
| rs768568622 | in-del | -/AAAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939219 | AAGACTCTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 55819 |
| rs768571134 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045646 | TTTTGACAGGGTGCT[C/G]ACTGGTGCGTTTACA | 55819 |
| rs768575148 | snp | A/C/G | 5.21553e-05 | 0.00510636 | missense, synonymous-codon | RNF130 | GRCh38.p7 | 5:180071654 | GGCTGCAGGTCAGCA[A/C/G]GGCGAGCGCGGCGAG | 55819 |
| rs768643770 | snp | C/T | 1.83431e-05 | 0.0030284 | intron-variant | RNF130 | GRCh38.p7 | 5:179970545 | TCACAAGTTACATAC[C/T]AAGAAACTTATTAGG | 55819 |
| rs768644432 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958229 | AAAGCATACAACCTA[C/T]TAATGGTTATACCAT | 55819 |
| rs768681078 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974937 | CCATTGCTTCCTCTG[A/G]GCAGTCAATGGTGAA | 55819 |
| rs768684090 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056369 | TTACTATAGAGAATG[A/G]GCTAGAAGGGAGCCA | 55819 |
| rs768756869 | snp | C/T | 1.67086e-05 | 0.00289033 | intron-variant | RNF130 | GRCh38.p7 | 5:180040442 | AATCAACAACCCTCA[C/T]TTTTGTTTACCTGGA | 55819 |
| rs768776470 | snp | A/C | 0.000214166 | 0.0103459 | missense | RNF130 | GRCh38.p7 | 5:179978226 | GAGAATTCGGACGAC[A/C]TCATTCTGCTTATAG | 55819 |
| rs768777793 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047415 | TAACATTTCTTTTTA[C/T]TACTTAGCTTCATTG | 55819 |
| rs768797323 | snp | C/T | 0.0001876 | 0.00968321 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920287 | AAATCACAAAAGCAG[C/T]GACCCCAACAGCCAG | 55819 |
| rs768807620 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036719 | AGTGCTACCCCTACT[C/T]CTCTGTTATTTTTAA | 55819 |
| rs768812346 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031043 | GGTGATGTGACCAAC[C/T]TCCACTTAATAAACA | 55819 |
| rs768824667 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948263 | GCATGCTACCTGGTA[C/T]ACCCTAAGTGATCAG | 55819 |
| rs768830660 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060129 | GGCAAGGAAATGATT[C/T]CCCCTGAGAGCTCCA | 55819 |
| rs768843989 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944756 | GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGT | 55819 |
| rs768853884 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008808 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 55819 |
| rs768860106 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014515 | ATAAGGTTTGTACAT[A/G]TCAATGTAAACCAAC | 55819 |
| rs768868371 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939174 | GTGAGCTGAGGTCGC[A/G]CCACTGCACTCCAGC | 55819 |
| rs768871935 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041998 | GCTTGAGCCATGATC[A/G]CACCACTGAACTCCA | 55819 |
| rs768877307 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975339 | CTGGAGGCAGTTTTG[G/T]TTGTCACAACTGTGT | 55819 |
| rs768916509 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954353 | AGTCAAGCGTCCATC[A/G]GCAGAACAAAATGTG | 55819 |
| rs768930895 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018223 | TTGCTTGAACAAGGG[A/T]GGTGGAGGTTTCAGT | 55819 |
| rs768937641 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037396 | TCCATGGCCCTCCAC[A/G]GAGTCTAGATTTAGA | 55819 |
| rs769056779 | in-del | -/ACAT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056726 | ATGTGTACAAAAGAC[-/ACAT]ACAATGCTCATGACT | 55819 |
| rs769068991 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003753 | AAGTACCTACGATGA[C/G]GTACAAAATTCTTCC | 55819 |
| rs769091298 | in-del | -/AT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949868 | AAGGAGCAATCTGTA[-/AT]CAATCGGATCACTGT | 55819 |
| rs769092377 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985149 | GAAACCCTTTACCCC[C/T]TAACTTTTTTTTTTT | 55819 |
| rs769100840 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029811 | CTCCTAAAGTGCTGA[C/G]ATTACAGGTGTGGGT | 55819 |
| rs769119957 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964184 | ACCCCTGCCGAGGAG[C/G]AGCACTGGCTGTCCA | 55819 |
| rs769128406 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985759 | TAGACCTGACTGCAT[C/T]TGCACAAAACAAATG | 55819 |
| rs769141679 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000800 | CAACTCTATTGATTG[C/T]CTACACGTTTTCTTG | 55819 |
| rs769154154 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032044 | AAACCTTTTGCCCGT[C/T]GTAAAACTAGGTTGT | 55819 |
| rs769172866 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961427 | TCCATGACTTAGATT[C/T]TGAGTCATGCAGGTA | 55819 |
| rs769174640 | in-del | -/CCAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968311 | CAAACAAACAAACAA[-/CCAA]ACAAAAAAAGAAGGC | 55819 |
| rs769219684 | snp | A/T | 1.64773e-05 | 0.00287026 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179978256 | GCTCTCTATGCAGAC[A/T]GCACAATGATCAAAG | 55819 |
| rs769243334 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962915 | GCCTGCTCTTTGGTC[A/G]CCATTTTGCCCATGG | 55819 |
| rs769279890 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985581 | AGTCCTACCCTGGCA[A/T]GGTACTTCCTAATTT | 55819 |
| rs769287608 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960367 | TATAATCAGTCGCAG[A/T]ACTAAATAAACAGTA | 55819 |
| rs769304143 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061557 | CAGCCCCTCTCCCAG[C/T]GTCTGATGGCTGCTA | 55819 |
| rs769403799 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980377 | AGATTCAGCATTCTG[A/G]TTGAAAAGTAAAAAG | 55819 |
| rs769437127 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963976 | TTCTGCAGGGCTTTC[A/T]TTCTTAGTCAAAGGC | 55819 |
| rs769452963 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057667 | ACCCCCGCAATACCG[C/T]GACAGAAGCTCCTGG | 55819 |
| rs769455303 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951651 | GGAACATTCTCCAGG[A/G]TAGACCATGTTAGGT | 55819 |
| rs769486134 | snp | C/G | 1.94229e-05 | 0.00311626 | missense | RNF130 | GRCh38.p7 | 5:180071666 | GCAGGGCGAGCGCGG[C/G]GAGCCGGGCAGGGCC | 55819 |
| rs769491185 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055877 | TCATCTGAGGTCAGG[A/C]GTTCAAGACCACCCT | 55819 |
| rs769498124 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064716 | TGACTCCCTCGCCCT[C/T]CCTAACTTTTCTCTC | 55819 |
| rs769508181 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949759 | TGGCTCTGCAGCCTG[C/T]GTCGCTTGGCACGCA | 55819 |
| rs769518120 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994617 | ATAAACAGCCTTAGT[A/G]TGGTGGCTTTCTCAA | 55819 |
| rs769518182 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066696 | CAAAAAATTAGCCGT[A/G]CTTGGTGGCACATGC | 55819 |
| rs769552890 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024794 | CATGAGTTTTGCCAT[C/T]CCCACTCCCTTCACG | 55819 |
| rs769594321 | in-del | -/GGATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057642 | AGGCGTATGCCAAGA[-/GGATT]ATTACACCCCCGCAA | 55819 |
| rs769607863 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037626 | GGGTCATATTCCAGA[C/G]TTACTGAATCAGAAT | 55819 |
| rs769630535 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921851 | CATAGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 55819 |
| rs769656351 | snp | C/G | 1.97975e-05 | 0.00314616 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015389 | GCTTTATAATCACAC[C/G]AGGTACAAACGGTTT | 55819 |
| rs769674408 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992493 | ATTCCTTCAATGAGT[A/G]TTTCATTTCCAGGAG | 55819 |
| rs769701036 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973220 | AGTCTCAAATTCCCA[C/T]GGCACATCCCTCGCT | 55819 |
| rs769715510 | snp | C/T | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:179980136 | GACTGTACCTTGTCA[C/T]CCTTCTTTACTGTCC | 55819 |
| rs769791806 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056766 | CATTGTTCTTAACCA[C/T]CAAAAAGCAGGAAAC | 55819 |
| rs769792039 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943416 | AGGGAGGGCCTGACG[C/T]GGACTTTCTACCTTC | 55819 |
| rs769794439 | snp | C/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073171 | AATGTTCTGAAAATC[C/G]GGAAAAGAGGTGGCT | 55819 |
| rs769799856 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179928082 | CACACAATTGATTGG[G/T]CTAATCTTTACGGAC | 55819 |
| rs769834464 | snp | C/T | 2.21139e-05 | 0.00332512 | intron-variant | RNF130 | GRCh38.p7 | 5:179970367 | TATTACACATACATA[C/T]AATAATATACAAAAG | 55819 |
| rs769844194 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059995 | CTGGGTGGGCCCAAT[A/G]TAATCACAAGTGTCT | 55819 |
| rs769844213 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | RNF130 | GRCh38.p7 | 5:180040492 | CCTCTTTGGATTTAT[C/T]ATTGTAGATGACTAC | 55819 |
| rs769882175 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984046 | GCACCATCTGCTTGA[C/T]GAAAATGCATTTTTT | 55819 |
| rs769887792 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942685 | CTGAAAGCCTAAGCC[C/T]TAGCTGTTTAAACTG | 55819 |
| rs769894459 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979487 | GCAGGAGACAGTTTT[C/T]GTTTTATGCCTTTTG | 55819 |
| rs769912099 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944774 | AAAAAAAAAAAGTTC[A/G]CATGGAGTAGGGCTA | 55819 |
| rs769932782 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027029 | GATCCGGGTTTCTCT[C/T]CTTTTGACTTTTACC | 55819 |
| rs769940188 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046239 | CGCCAAGCTCACACC[C/G]ACGCAGAACTCCAGG | 55819 |
| rs769948387 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931639 | CCGGGCGTGGTGGTG[A/C]CTGCCTGTAATCCCA | 55819 |
| rs769949929 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041716 | GGTCCTCTGTGTGCC[A/G]GGAAGGAAGTAAGGA | 55819 |
| rs769967816 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013539 | ACATAAGGCATAGAA[C/T]GACTGCAGTGTTAAG | 55819 |
| rs770003857 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021296 | CCTGGCCAAAATCTA[A/G]ATTTCTAAACATCTG | 55819 |
| rs770016485 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968285 | GGCGACAGAGCAAGA[-/CT]CTGTCTCAAAACAAA | 55819 |
| rs770022734 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027633 | TGTCCCTCTCATCCT[A/G]AGCACCCACTCCATT | 55819 |
| rs770041480 | snp | G/T | 1.65444e-05 | 0.00287609 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955647 | CAGAAAGCAGGTTTT[G/T]TCTTCTTCAAAACCA | 55819 |
| rs770053527 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052165 | TCTCAGTGGACAGTA[C/T]CATCCACTCCCCTGC | 55819 |
| rs770061414 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | RNF130 | GRCh38.p7 | 5:179966968 | GGGTTCTGGTGAGCC[C/T]TTCCATATCGAATGC | 55819 |
| rs770066694 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015562 | GGGGAAGGAGTAGGG[-/A]AAGGAGTAGGGAAAG | 55819 |
| rs770074057 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937428 | GATGTATGAGTGGCT[A/T]ACTTAATGCACGTAA | 55819 |
| rs770091783 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006362 | TGCAAAGTTTTAACC[C/T]TTCTCTGACACAGGA | 55819 |
| rs770129018 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964455 | AACTATAAAATATTT[A/C]TTTGAGTACACACTG | 55819 |
| rs770135310 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924457 | CTGAGATTGTGCCAT[C/T]GCACTCCAGCCTGCG | 55819 |
| rs770145371 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040710 | AAGTCTTTATCAAAG[A/T]GTCAACTGCTTTCTG | 55819 |
| rs770148423 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989799 | TAAATTCTTTGTTTT[-/A]TTTTTTCTTCTGTCT | 55819 |
| rs770149530 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069509 | AAAACTCAAGGGGAC[C/T]GACTTCACACCCAGT | 55819 |
| rs770182564 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982522 | AATACATGAAAATTA[C/T]AGTTCCTCCACATTC | 55819 |
| rs770196490 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958902 | GCTAGGCTTGTCTTG[A/G]ACTCCTGACCTCAGG | 55819 |
| rs770199105 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020439 | CTCAGCACCCACAGA[C/T]GCACAGCAAAGACCA | 55819 |
| rs770215165 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969470 | CTGGAACAGAGTCAA[C/T]AGCATACAGCCTACC | 55819 |
| rs770218540 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987882 | GCTTCGTACTGGGTT[A/G]AGGCTTTTTGTGTCT | 55819 |
| rs770229319 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938816 | GACTCACCCTGGCAA[C/T]GTTAACTTCACAGCA | 55819 |
| rs770237758 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937599 | ACCCTTATACATTGT[C/T]GGCAGGAATGTAAAA | 55819 |
| rs770240344 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977680 | AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT | 55819 |
| rs770246064 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050829 | TTTTTATTTTTGGAG[A/G]CAGGGTTTCACTCTG | 55819 |
| rs770253141 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041410 | GGCCACTGTTCTGGA[-/T]TTTTTTGGGATAGTT | 55819 |
| rs770269470 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996811 | TGGTATTGCTATTAG[A/G]GTAATGCTGGCCTTG | 55819 |
| rs770280166 | in-del | -/T | 1.66424e-05 | 0.0028846 | intron-variant | RNF130 | GRCh38.p7 | 5:180040448 | CAACCCTCATTTTTG[-/T]TTACCTGGATGAGTC | 55819 |
| rs770281274 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021781 | CAAAATTTATAAACA[C/T]AATACAACCCCCAAA | 55819 |
| rs770297010 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009970 | GAAAGTATCTTGGCC[A/G]GGCGCAGTGGCTCAC | 55819 |
| rs770299135 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949268 | ACCGTGCCCAGACAA[-/T]TTTTTTTTTTTTTTA | 55819 |
| rs770313793 | in-del | -/T | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954894 | GCATATAATTCGATG[-/T]TAACAAAGTATTTTG | 55819 |
| rs770318194 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013151 | CATCAAAACAATAAA[A/G]GATATTGACACGAAG | 55819 |
| rs770322625 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995656 | ACTCCCTAAGTAAGA[C/T]CCAGGGCTTGGGAAG | 55819 |
| rs770322977 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007481 | CCTTTGCTAATATTA[C/T]GGCTTCTCTTTTAAA | 55819 |
| rs770348123 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024689 | TAAAAAAAGGGAAAT[A/G]ACACCAAACGGAAAC | 55819 |
| rs770388998 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942309 | AACTGAAACACTCAT[C/T]AGTTGAGGACTGATT | 55819 |
| rs770409073 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070360 | AGTCTGAGTTGCGGA[C/G]AGGCTACAGTAAAAG | 55819 |
| rs770414937 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989678 | TAAAAAAATCTATTC[A/G]GTCAGGCTGTATCTT | 55819 |
| rs770418766 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967165 | GCCCACCTACCTACT[C/T]CTTCTTCTCTCACCC | 55819 |
| rs770438801 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067237 | CCTCCATGAAGGTGA[-/T]TTTTTTTTTAACCCA | 55819 |
| rs770479108 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009311 | AGAGGTTGAACAAAA[C/T]AAAATACAGACTGGG | 55819 |
| rs770495275 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961771 | GGTTTGAATCACAGC[C/T]ACTCACAGAGCTACT | 55819 |
| rs770515766 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926791 | AACACTTGGGCTTGC[A/G]CTGGGCATTGGACGT | 55819 |
| rs770516924 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031297 | TTTGAGACCAGCCCG[A/G]CCAGTATGGCGAAAC | 55819 |
| rs770523351 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985768 | CTGCATTTGCACAAA[A/G]CAAATGCCTGAAGTC | 55819 |
| rs770563624 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056545 | CACACTGGGCAGAGG[A/T]GGTGTTACCGACAGA | 55819 |
| rs770567196 | snp | A/C | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073687 | TGGAGAACGGCTTTT[A/C]CTTATTTACTTATCC | 55819 |
| rs770589045 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990764 | AGGGCTCACACTCTT[C/G]TCTTCTGGTCACTTC | 55819 |
| rs770589718 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068047 | AAAATTATTCTCTAA[C/G]GCTGTAACATCCAAT | 55819 |
| rs770610722 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055541 | TGTCCTAAATAAAGA[C/G]AGGGATTTCTGAAAT | 55819 |
| rs770619045 | snp | G/T | 1.64741e-05 | 0.00286998 | missense | RNF130 | GRCh38.p7 | 5:179980157 | TTTACTGTCCTGGTT[G/T]TCAATTTACTGATGG | 55819 |
| rs770664735 | snp | A/G | 6.77736e-05 | 0.00582084 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040637 | TGGATCACAGCCCAG[A/G]TGATCAGCAACTGAA | 55819 |
| rs770678465 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036481 | GCAGAAACTCCACAC[A/T]GCATAGCTTGGGGAG | 55819 |
| rs770681983 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948744 | AATAATTTGGAAGAT[-/AA]AAAGTCAAGGAAGCT | 55819 |
| rs770688032 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987744 | ATTTGTTGTTCCTTT[A/G]TTCTGTTGATGTGAA | 55819 |
| rs770690555 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018399 | ACAATCATGGCAGAA[-/G]GCACCTCTTCACAGG | 55819 |
| rs770718100 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003628 | AACCTGTGACAGGTA[C/T]AAGTGTCTATGTATG | 55819 |
| rs770719845 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996609 | GTTGATGTGATGCAT[C/T]GCATTTATGGATTTG | 55819 |
| rs770740093 | in-del | -/GTC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990764 | AGGGCTCACACTCTT[-/GTC]TTCTGGTCACTTCTC | 55819 |
| rs770763802 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925881 | CCCAGAACACAGACT[C/T]CATATAGACGGAGAA | 55819 |
| rs770799016 | snp | A/T | 0.000185856 | 0.00963813 | missense | RNF130 | GRCh38.p7 | 5:179920405 | CGAGGGGACAAGGAG[A/T]TTCGATGAAAGAAGT | 55819 |
| rs770835914 | in-del | -/AG | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072559 | GACGGGTTTCCAGGA[-/AG]AGAGTTTTTCCAGGG | 55819 |
| rs770906756 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057563 | AAAAAAAAAAAATCA[C/T]GTGTAATGTGTAATG | 55819 |
| rs770911318 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037419 | GATTTAGAGTCACAA[C/G]AGGCCTTACAGAAGG | 55819 |
| rs770915697 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979117 | TGGGTAGGTTAAATC[C/T]GCTCCAGGGAATTTC | 55819 |
| rs770947099 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991252 | TTTTCCTTCACACTG[A/C]CTTTAAGCAATCTGA | 55819 |
| rs770950062 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066608 | ATTAGCCAGGTATCG[A/G]GCAGATCACCTGAGG | 55819 |
| rs770951596 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180040517 | GACTACAGCAACTGC[A/G]TTGTGGAAAGCGGCC | 55819 |
| rs770955375 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023136 | AAAGGAGAGAGAGCT[A/G]CAATGATCCATGTGG | 55819 |
| rs770959853 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056218 | CCGCTGTTACTCTTA[C/G]CCTAAGTGTTGAGCC | 55819 |
| rs770978323 | snp | G/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955223 | GAAATTATCACAGAG[G/T]GAATGTCCCCCTTGA | 55819 |
| rs771001842 | snp | A/C | 2.10555e-05 | 0.00324458 | intron-variant | RNF130 | GRCh38.p7 | 5:179970380 | TATAATAATATACAA[A/C]AGTGGTAACAAATAA | 55819 |
| rs771004966 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065556 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 55819 |
| rs771014735 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026544 | TTTCCTGTCAATGAC[A/G]TCATGGACAGGGCAC | 55819 |
| rs771025031 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960744 | GTTTAGTATCAATTT[C/T]TGGACAGTCATTAAA | 55819 |
| rs771030419 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983898 | TATTTGTTGATGCTA[C/T]GGAAAATGGGATTTC | 55819 |
| rs771048341 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956782 | CACTCTCCAGCCACA[G/T]CAGTACGCACATGAG | 55819 |
| rs771094308 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969200 | TATACATGCTTCTCT[C/T]AAGCAAGGGCTAACG | 55819 |
| rs771099126 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040154 | CCTGGGCGAATGATT[A/C]CAAATCAAATACATT | 55819 |
| rs771101407 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070394 | TATGTGATTATTTTT[A/C]CCCAGCCAGACTGTC | 55819 |
| rs771101632 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057970 | ACCTGTGGGGTCTGC[A/C/G]CTAACTTTACCAGGT | 55819 |
| rs771103454 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061299 | CAACTGACGTGACTT[A/C]AGGCACATCCAGAAG | 55819 |
| rs771120399 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027446 | AGTCAGAAGAGGATC[A/G]TAATTCTGGAGATTT | 55819 |
| rs771154101 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038916 | CAGCATGGAATGAAG[A/G]TAAGTTACATTAGGC | 55819 |
| rs771156589 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059836 | AGAGAGGCAGAACGA[C/T]GGCTCCCTCAAAGAC | 55819 |
| rs771173047 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943668 | AATAACTTACTCAAA[A/C]TCATAAAGCTAAAAC | 55819 |
| rs771175053 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958726 | AGTTTCACTCTGGTC[A/T]CCCAGGCTGGAGTGC | 55819 |
| rs771203179 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923281 | AATTGTTCCGTCGTC[A/G]ATTGTTTAAAAGATT | 55819 |
| rs771241785 | snp | A/G | 3.51655e-05 | 0.00419303 | intron-variant | RNF130 | GRCh38.p7 | 5:179970522 | CTATAAAATAATGGA[A/G]AATTATGTCACAAGT | 55819 |
| rs771248113 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974113 | AGAACCTGGCAAATA[A/T]AAAAGGATGCAGGAT | 55819 |
| rs771260817 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018359 | ACACACAGTTCCACA[G/T]GGCTAGGGAAGCCTC | 55819 |
| rs771279708 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940873 | ATCTAAAGACTCATG[C/T]CTTTTTCTGTATTTT | 55819 |
| rs771290605 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975899 | ACCTTGGTGGCAGGC[A/G]TGGCTTTGCAGCACG | 55819 |
| rs771346739 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067545 | TTAAAAAAATTCAAA[C/T]ATTTATAGGCTAATG | 55819 |
| rs771362349 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061474 | TCATTGTCTCACAGT[C/T]CTGGGGCCCCAAAGT | 55819 |
| rs771376339 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949864 | CCTCAAGGAGCAATC[C/T]GTAATCAATCGGATC | 55819 |
| rs771391419 | snp | C/T | 1.64806e-05 | 0.00287054 | intron-variant | RNF130 | GRCh38.p7 | 5:179966779 | GGCAGCCACATGCCC[C/T]GTGCCTGAGCGGAGG | 55819 |
| rs771445410 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978870 | CAGGTATTCAGACAC[C/G]AGATTAATTGATTTC | 55819 |
| rs771488810 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926605 | GTGAGCCGAGATAGC[A/G]CCATTGCACTCCAGC | 55819 |
| rs771492201 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004920 | TTCATTCATTCACCA[A/C]CATTTTTTCCCATTT | 55819 |
| rs771509745 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937502 | AACCATGATGAAATG[C/T]CATTCACACTCATTA | 55819 |
| rs771516098 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021896 | CAGCAGCCCAGGTCC[G/T]AGTCACATGCTACAC | 55819 |
| rs771517110 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036323 | TTTTTAATAAGACTG[A/G]TTTCCTAGGAACTGC | 55819 |
| rs771519033 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065407 | GTGTAACACTCCACT[A/G]AGTGGATATATCATA | 55819 |
| rs771523025 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954109 | ACTGGTGTTATGGAG[A/G]TTGTGAAGAAATTGC | 55819 |
| rs771535134 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955694 | AAAAGGAAAAAAGAG[A/G]TCATAAATTAAAGAG | 55819 |
| rs771549330 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944275 | CACCCAGCCTTATTT[C/T]TAATAAATTTTAAGT | 55819 |
| rs771575379 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983333 | CAGGTACAGATGAAC[-/T]TTTTTTTTTTTTTTT | 55819 |
| rs771593348 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066461 | CCTTCCCAATATGAC[C/T]AATATACTCCCCAAC | 55819 |
| rs771597640 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935938 | GCAGTTGATGTCAAG[C/T]GGTCTCCACAAGGGA | 55819 |
| rs771624582 | snp | C/T | 2.55836e-05 | 0.00357647 | intron-variant | RNF130 | GRCh38.p7 | 5:179963432 | GTGTTTTCCTGGGAT[C/T]ATCTGGCACATGCAA | 55819 |
| rs771626208 | snp | C/T | 1.8149e-05 | 0.00301234 | intron-variant | RNF130 | GRCh38.p7 | 5:180013320 | CCAGTGCCTGCAATA[C/T]AAAATAAATATATAA | 55819 |
| rs771645081 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042026 | CCAGCCTGGGTGATA[C/G]AACAAGACCTTGTCT | 55819 |
| rs771645667 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940370 | GGATTACAGGTGCCC[A/G]GCACCACACCCAACT | 55819 |
| rs771650521 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938989 | TGCCCAAAACTTTGC[A/G]AGGCTGAGGTGGGCA | 55819 |
| rs771685380 | snp | C/T | 5.12781e-05 | 0.00506324 | intron-variant | RNF130 | GRCh38.p7 | 5:180013025 | ACTGTGAACTCTGGC[C/T]GTTACGAACCAATCA | 55819 |
| rs771687362 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055114 | TTGGGTGGCCAAGGC[A/G]GGCAGATCTCATGAG | 55819 |
| rs771687516 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007883 | TGAGCTACACCCAGT[C/T]CACTAACACAGGCTT | 55819 |
| rs771727063 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979888 | TCCTGGCTTTTTAAC[A/G]CACAAATGGTCCCAC | 55819 |
| rs771731184 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070511 | CAAATCATGACTTTA[G/T]TTAGGTTGCCTACTT | 55819 |
| rs771743111 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021979 | TTCTTGGTGTTTGTG[A/G]CCTTGGCACTTTCGA | 55819 |
| rs771766349 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013370 | TTATGGAAACATCAA[A/C]TGTATCAACACGCTA | 55819 |
| rs771804616 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001823 | CCAAGAGGAAGGTTA[A/T]CTAAGCAGCTGAGCT | 55819 |
| rs771809531 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045879 | TCCTTTAGCTAGACA[C/G]AAAAGTTCTCCAAGA | 55819 |
| rs771898922 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058855 | GCTGAGCCACTGCAC[C/G]CAGCTGGTATAATGG | 55819 |
| rs771918897 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009049 | GCATAGCCTTAAAGA[A/G]GTGCTGAGAGAGAAA | 55819 |
| rs771927299 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976400 | GACAGAATTTGGAGA[A/G]CCTTGGCTTCTCCTG | 55819 |
| rs771947378 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974455 | GAGGAGGCCCCTCCG[A/C]CATGCCAACTGCCAT | 55819 |
| rs771947468 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964381 | AACATTTTAAAAACA[A/G]TATTTATTGAGAACC | 55819 |
| rs771992161 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011631 | AATTAGCCAGTCATG[G/T]TGGTGCATACCTTCA | 55819 |
| rs772020819 | snp | A/G | 3.56449e-05 | 0.00422151 | intron-variant | RNF130 | GRCh38.p7 | 5:179970532 | ATGGAGAATTATGTC[A/G]CAAGTTACATACCAA | 55819 |
| rs772050508 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003979 | TCACAAGTACTGACT[C/T]GTGTTATCGTCACAA | 55819 |
| rs772067132 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932507 | TCAAATGATCCGCCC[A/G]CCTCAGCCTTCCAAA | 55819 |
| rs772109832 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920581 | ATACAAAAAGTGCGG[A/G]CATCCTTCAATTCAC | 55819 |
| rs772129408 | snp | C/T | 2.32875e-05 | 0.00341221 | intron-variant | RNF130 | GRCh38.p7 | 5:180040680 | TACACACATTAAAGA[C/T]AAATAAAACTGACCA | 55819 |
| rs772130006 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038656 | TCAAGGAACACAGCT[C/G]GGAAATGCTGCATTG | 55819 |
| rs772143138 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004723 | ATGGTTCAGAGTATA[C/T]TGAGGATAGGTCACT | 55819 |
| rs772173387 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956739 | CAGCTCCGCAGGCAT[A/G]ACCCAGAAGGGCCTT | 55819 |
| rs772180561 | snp | A/G | 3.7482e-05 | 0.00432892 | missense | RNF130 | GRCh38.p7 | 5:180071554 | CGAAACGTGAGCGGG[A/G]CGCCGCGGCCGGGCT | 55819 |
| rs772184374 | snp | C/T | 5.37398e-05 | 0.00518334 | intron-variant | RNF130 | GRCh38.p7 | 5:179970398 | TGGTAACAAATAAAA[C/T]AGGAAACGTACCACA | 55819 |
| rs772195855 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063467 | GGTAGCAGATAGGGA[A/G]GTGAAAAAATGAATC | 55819 |
| rs772200353 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018201 | TCGGGAGGCTGAGGC[A/G]GAAGAATTGCTTGAA | 55819 |
| rs772244299 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067965 | TAAACATGAAAACCT[A/G]AGATTCACTTTTTTG | 55819 |
| rs772274149 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050432 | CCACCCACATTATGG[A/G]GAGCAATCTGCTTTA | 55819 |
| rs772281901 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024998 | CCTGGGAGGTGAAAC[A/G]CTCTGTAATACAAAA | 55819 |
| rs772283617 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999696 | CACTCCAGCCTAGGC[A/G]AGCAAGCGAGACTCC | 55819 |
| rs772290958 | snp | A/C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968274 | CACTCCAGCCTGGGC[A/C/G]ACAGAGCAAGACTGT | 55819 |
| rs772295122 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040357 | TAATAGGATTATGTT[G/T]GAAATTACATGGCTT | 55819 |
| rs772302827 | snp | C/G | 0.000158904 | 0.00891216 | intron-variant | RNF130 | GRCh38.p7 | 5:179963581 | TGTTGACAAAGGAAA[C/G]GGAGGAAATCACTCT | 55819 |
| rs772327369 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048541 | ACTTTGGGAGGCTGA[A/G]GTGGGAGAATCCCTT | 55819 |
| rs772397153 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031177 | TGAGGCTTTTGGTCA[A/G]CAGCAAGCTATTAGT | 55819 |
| rs772400306 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981326 | CACTCTAGACACATC[C/T]AGGCCTTACACTGTG | 55819 |
| rs772410398 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995331 | ACCTCTCAGGCAAAT[A/C]TCCTGCTCCAGTCCC | 55819 |
| rs772430750 | in-del | -/G | 1.65699e-05 | 0.00287831 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015292 | TGTTCAACGGGCCAT[-/G]ATCTGTGGTATAAGA | 55819 |
| rs772446013 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043180 | AAACAAAAAAATTAG[C/T]TAGGCATGGTGGCAC | 55819 |
| rs772471683 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959245 | AGCTCTCATCTTACC[C/T]GGTCCCCTCTCTTCC | 55819 |
| rs772474307 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011733 | GACTGCCACCACACT[C/G]CAGCCTGGGTGACAG | 55819 |
| rs772513583 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987530 | CTATGTGGAACAGAG[G/T]GGGTGGTAGGTAGAA | 55819 |
| rs772539377 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179975557 | TGTCGCTACATGGCA[A/G]TGAGATGGTGTGCTG | 55819 |
| rs772553301 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061443 | CACAAACTTGGTGGC[C/T]TAAAACAACATAGTC | 55819 |
| rs772555063 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982150 | GGAATAGATACAGTA[C/T]GTACTACTGTGTGTA | 55819 |
| rs772578085 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027427 | GAGAGTTATGGCATA[C/G]GAAAGTCAGAAGAGG | 55819 |
| rs772609916 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980297 | AAAGTCTCTATTTTA[C/T]TACATCCCTCTCCAT | 55819 |
| rs772623654 | in-del | -/CTTTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940029 | TTCTCTCTGCTTCTT[-/CTTTA]GTCTCAGGACTTTTA | 55819 |
| rs772635280 | in-del | -/T/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985152 | CCCTTTACCCCCTAA[-/T/TT]CTTTTTTTTTTTTTT | 55819 |
| rs772650924 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949710 | AACTCAAAGCTGTTG[C/T]AACTTTAAGTTATCC | 55819 |
| rs772665362 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061381 | CATGCCTGTGTTCAA[C/T]GCTGGGATTCTCTTT | 55819 |
| rs772668218 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179925047 | CATATTGTGAAAAGT[A/G]TATTTGGTTTTTATC | 55819 |
| rs772711799 | snp | C/T | 1.87633e-05 | 0.00306289 | intron-variant | RNF130 | GRCh38.p7 | 5:179970556 | ATACCAAGAAACTTA[C/T]TAGGCCAAAATGGAA | 55819 |
| rs772712665 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179940494 | CTCCCGCTTTGGCCT[C/T]CCAAAGTGCTGGGAT | 55819 |
| rs772714018 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043218 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGATGGG | 55819 |
| rs772715239 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979048 | ACAAACTAAGATGAA[C/T]TGGCTTTAATAATTA | 55819 |
| rs772723910 | snp | A/C | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072648 | TTAGATTCTCGTAAG[A/C]AGTGGGCAACCTAGG | 55819 |
| rs772765896 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971196 | CTTAAAAAAAGGAAC[A/T]TGTGCCCTCCGGAAG | 55819 |
| rs772767109 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055292 | AAAACAAAAAAAAAC[A/C]GCAAACAAACAAAAA | 55819 |
| rs772771168 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031418 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAA | 55819 |
| rs772783432 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972178 | GGGCCAGCTGGACTT[C/T]CCAGCAGGGGTCAAG | 55819 |
| rs772794126 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030706 | AATCTTCATGCCCAG[-/CT]CTCTACCCTACACAG | 55819 |
| rs772821516 | snp | A/T | 1.96527e-05 | 0.00313464 | missense | RNF130 | GRCh38.p7 | 5:180071668 | AGGGCGAGCGCGGCG[A/T]GCCGGGCAGGGCCCG | 55819 |
| rs772827850 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982708 | CTTCAGCCTCTGGAA[C/T]AGCAGGAACTACAGG | 55819 |
| rs772829958 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030218 | TACTCAAAATACAAA[C/T]AAAAGTAAAAAAAGA | 55819 |
| rs772830142 | snp | A/G | 2.02014e-05 | 0.0031781 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015391 | TTTATAATCACACCA[A/G]GTACAAACGGTTTTA | 55819 |
| rs772833008 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009140 | ACTTAAATGTAAAAC[A/G]TAATATAAAACTTCC | 55819 |
| rs772835041 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997299 | GGTGCACACCAACAC[A/G]CCTGGCTTATGTTTT | 55819 |
| rs772877525 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002595 | GTGGGAACCCTGGTG[A/G]TGAGGTCTGTAGGTA | 55819 |
| rs772933288 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998323 | CTCCTTCCTAATTTA[C/T]TCATTGACCCACTGG | 55819 |
| rs772961220 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960577 | CCCTAGACCACCTGG[A/G]TCCCACACACTGCCC | 55819 |
| rs773001325 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939054 | GCCAACATGGTGAGA[A/C]CCCATCTCTACTAAA | 55819 |
| rs773004207 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180028249 | CCACAGTCATGACTT[C/T]GTACTCAATGTTCAT | 55819 |
| rs773015547 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949771 | CTGCGTCGCTTGGCA[A/C]GCAGCTGCAACTTCT | 55819 |
| rs773017598 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052559 | CTTCTTTCTTCTAGT[A/G]TGAGTATTTCCAGTA | 55819 |
| rs773030093 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932280 | GTCTTTTATTTGAGA[A/G]GGAGTCTCGCCCTGT | 55819 |
| rs773044487 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992391 | TCGTGATCCACCCAC[C/T]TCATCCTCCCAAAGT | 55819 |
| rs773068963 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064526 | CTTGGTTTGCCAACT[C/T]TGGAAATTGTGTGCA | 55819 |
| rs773077018 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051516 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 55819 |
| rs773084448 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977985 | CGCGTGCCACATCGC[A/G]TATTGGCTACACCTC | 55819 |
| rs773126673 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | RNF130 | GRCh38.p7 | 5:180040495 | CTTTGGATTTATTAT[C/T]GTAGATGACTACAGC | 55819 |
| rs773151023 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058896 | TCCATTTTGCAAGAC[-/AA]AGAGTTCTGTAGATG | 55819 |
| rs773192193 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065494 | GGCCGGTCACGGTGG[C/T]TCACACTTGTAATCC | 55819 |
| rs773195266 | in-del | -/CAGCTTATG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947525 | ACAGACCCTGGGGGC[-/CAGCTTATG]CAGCTTATGTGTTGA | 55819 |
| rs773215945 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004807 | AATTAGAGTAAGTCT[G/T]TATCTGCACAGAGTA | 55819 |
| rs773221188 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955813 | CCAGGAAGCCATTAA[A/G]TGTTTTCCCAAAATC | 55819 |
| rs773274210 | in-del | -/CTTA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034515 | TCCCCAATTCAATTT[-/CTTA]CTTATTATAGCTACT | 55819 |
| rs773310864 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025043 | GCAAAAGGACTGTCC[C/T]AAAATACCCCTGCCT | 55819 |
| rs773315694 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967391 | AAGAATCCCAGGTAA[C/T]AGAAAACACCTCTTT | 55819 |
| rs773334107 | snp | A/G | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954792 | AACCCGTTTTCAATA[A/G]GAATACGTTCTCACT | 55819 |
| rs773370068 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942962 | AGCAATTTGAGAGGC[C/T]GAGGAGGGTGGATCA | 55819 |
| rs773389244 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953117 | GAATCCACAAAAAAA[-/T]ATGAGAATAAATGAG | 55819 |
| rs773403461 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | RNF130 | GRCh38.p7 | 5:179966976 | GTGAGCCTTTCCATA[C/T]CGAATGCTACGTTAT | 55819 |
| rs773416062 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069204 | AGGTAGGCTAACTTA[A/C]AAAGATCCCAGCAGA | 55819 |
| rs773438058 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026437 | AAGAACCCATAACGT[C/T]CCCTTCATACTACCA | 55819 |
| rs773448575 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067981 | AGATTCACTTTTTTG[A/G]GTTTTATTGTATCCC | 55819 |
| rs773455903 | snp | A/G | 2.58481e-05 | 0.00359491 | intron-variant | RNF130 | GRCh38.p7 | 5:179963428 | CCATGTGTTTTCCTG[A/G]GATCATCTGGCACAT | 55819 |
| rs773472075 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961590 | CTATTAAACTACCCA[A/G]TAATTCTCGAAAAGT | 55819 |
| rs773475014 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058129 | CGGTGTCAAAGCGAG[A/G]ACAGAAGTTACTGCT | 55819 |
| rs773491596 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956760 | GAAGGGCCTTTGCGT[A/G]CTCCCTCACTCTCCA | 55819 |
| rs773518582 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981328 | CTCTAGACACATCCA[A/G]GCCTTACACTGTGGG | 55819 |
| rs773519031 | in-del | -/T | 3.30907e-05 | 0.00406746 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955643 | CAGTCAGAAAGCAGG[-/T]TTTTTCTTCTTCAAA | 55819 |
| rs773564198 | snp | C/G | 0.000181218 | 0.00951714 | missense | RNF130 | GRCh38.p7 | 5:179966896 | TTCGAAGTGGCTCAA[C/G]GCCAAGGGAGTTGTC | 55819 |
| rs773573028 | snp | A/G | 1.6543e-05 | 0.00287597 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955637 | CAAAATCAGTCAGAA[A/G]GCAGGTTTTTTCTTC | 55819 |
| rs773595179 | in-del | -/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072994 | CACATCGCTATAAAG[-/T]TATCAGCTAAAAGGA | 55819 |
| rs773634864 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031185 | TTGGTCAACAGCAAG[C/T]TATTAGTAATTAAAT | 55819 |
| rs773635638 | in-del | -/AG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957791 | CAATACACCTCAAAC[-/AG]AGGTTAATTTTAAAT | 55819 |
| rs773643386 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179932575 | TTAGCTAATATTTTC[G/T]TAAAACATTTACGTC | 55819 |
| rs773645600 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948427 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGA | 55819 |
| rs773650566 | in-del | -/AAACAAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968294 | AGCAAGACTGTCTCA[-/AAACAAAC]AAACAAACAAACAAA | 55819 |
| rs773666019 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013160 | AATAAAGGATATTGA[C/T]ACGAAGACTAGAGAG | 55819 |
| rs773730031 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003988 | CTGACTCGTGTTATC[A/G]TCACAATCATTTTAT | 55819 |
| rs773736545 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920618 | TTTAAGCATCTAAGT[A/T]CCAATCTTCGGATCC | 55819 |
| rs773737153 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947126 | GAATCTTCTCATCAC[C/T]GACACAACTGTCTTC | 55819 |
| rs773746214 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977009 | CTGTTTCCAGGGCAA[C/T]CAGGCACAGGCGAGT | 55819 |
| rs773781103 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964577 | TGTTTTATGCACAAG[C/T]TGTATACAGCATGTG | 55819 |
| rs773785615 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016700 | CTACTTTAATAAACA[A/C]TTCTATTCTTTCCAC | 55819 |
| rs773822938 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180048689 | AGGGCTGTATTTTGC[A/G]GTGAAGAATTCAGCA | 55819 |
| rs773823273 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935850 | CTAATATAAATGAGT[A/G]CTTTGACTCCTTCCT | 55819 |
| rs773829149 | snp | C/T | 1.6998e-05 | 0.00291525 | intron-variant | RNF130 | GRCh38.p7 | 5:180013041 | GTTACGAACCAATCA[C/T]TGTTGAGTACTGAGC | 55819 |
| rs773839904 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007868 | CCAACGTCCTCAGGG[A/T]GAGCTACACCCAGTC | 55819 |
| rs773846848 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952717 | TGCACCACATTCATA[A/G]GATAGAATAGAATAA | 55819 |
| rs773856851 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064104 | GACCTATTATAATAA[A/G]TTATTTTATGTCCAT | 55819 |
| rs773857515 | snp | A/G | 0.000185891 | 0.00963903 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179920413 | CAAGGAGTTTCGATG[A/G]AAGAAGTGACCACCT | 55819 |
| rs773872756 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046277 | TCGGCCAGCCCAGAG[A/C]GGGGCTCCCACAGTG | 55819 |
| rs773892668 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018881 | CTCCTGGGAGTAAAC[C/G]CCGGGGCAAGCCCAG | 55819 |
| rs773899024 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046135 | GACCGCGGCGCGTGC[A/T]GGCCCACAGTGCTGA | 55819 |
| rs773912696 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060133 | AGGAAATGATTCCCC[-/CT]GAGAGCTCCAAAGCC | 55819 |
| rs773957625 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924967 | GCACTAAGGGAGGAA[G/T]ATGAAAAACAAAGAG | 55819 |
| rs773958523 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057913 | CCACTACCTACAACC[A/G]GTGTCTGAAGTAGGG | 55819 |
| rs773961437 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053685 | TACTGCCCAGGGCCA[A/G]CTAAATGATGGATGG | 55819 |
| rs773968771 | snp | G/T | 1.64814e-05 | 0.00287061 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179966981 | CCTTTCCATATCGAA[G/T]GCTACGTTATCAGTA | 55819 |
| rs773971678 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040982 | CAGACGAGAAACCCA[G/T]GTGACTGATGTAACC | 55819 |
| rs773973804 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964802 | TATTAAAATGCTTAG[C/T]AAACCCCTATCTTTT | 55819 |
| rs774024767 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052328 | ACATGTGACGTCTTT[A/C]CAGTGTAGAGTTCTG | 55819 |
| rs774045775 | in-del | -/CAAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968309 | AAACAAACAAACAAA[-/CAAAC]AAAAAAAGAAGGCGG | 55819 |
| rs774073912 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020517 | TGCTGGGAAGCCGAA[C/T]GTGTAAGCCACTGAG | 55819 |
| rs774073995 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035156 | CTTTGTTTACTGACC[C/T]AGGTATTTAAAGCTA | 55819 |
| rs774114039 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179989161 | AGGAGAAACGCCAGA[C/T]GCTTATAAAACTATC | 55819 |
| rs774120712 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000858 | AATTTTGAATTCCTT[C/T]TCTGGCAATTCATTA | 55819 |
| rs774126266 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950136 | TTTTTTTCTTGAGAT[A/G]GAGTCTCACTCCATC | 55819 |
| rs774138059 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005773 | AAAGAATAACTCCTA[A/T]ACCACACAGTATTTT | 55819 |
| rs774186474 | in-del | -/CTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949652 | CAACTTTATACATTG[-/CTT]CTATTTGTAAATCTG | 55819 |
| rs774197826 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964063 | AGCCGGCCTCCCATG[A/G]CATCCATGGCTACAT | 55819 |
| rs774228009 | snp | A/G | 1.95957e-05 | 0.00313009 | intron-variant | RNF130 | GRCh38.p7 | 5:180040661 | AACTGAAAAGAAAAA[A/G]AAATACACACATTAA | 55819 |
| rs774253008 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934403 | ATTATTTTTAATGTC[C/T]GTAGGCTTTGCAGTG | 55819 |
| rs774260167 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952564 | ATTAATTACATATCA[A/C]TATCCCTTATAAATA | 55819 |
| rs774260249 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044564 | CATGGCCGGGCGCGG[C/T]GGCTCACGCTTGTAA | 55819 |
| rs774268510 | snp | A/C/G | 6.22108e-05 | 0.00557693 | intron-variant | RNF130 | GRCh38.p7 | 5:179970382 | TAATAATATACAAAA[A/C/G]TGGTAACAAATAAAA | 55819 |
| rs774293204 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982366 | CATTCTCAATTCTTT[C/G]CATGGACATATGCTT | 55819 |
| rs774315234 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974649 | CTCACGGAGGGAAGA[A/G]GCAGTGGGCAGGTGT | 55819 |
| rs774352723 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179923567 | CAGCCAATCCCAGCG[A/G]CTGAGTTTCAGCCAA | 55819 |
| rs774377806 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959120 | TAAACCAGGCAATAC[A/G]GGTAAAAGAGACCAG | 55819 |
| rs774401470 | snp | C/T | 1.64743e-05 | 0.00287 | missense | RNF130 | GRCh38.p7 | 5:180040518 | ACTACAGCAACTGCA[C/T]TGTGGAAAGCGGCCC | 55819 |
| rs774440816 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036732 | CTTCTCTGTTATTTT[C/T]AATCCTACCTTATAA | 55819 |
| rs774462041 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955137 | GCAGGGGCACAGTGG[A/G]GAGCAAATGTTACAA | 55819 |
| rs774472381 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954437 | CAACATGTATGAACC[A/G]TGAACACATGCTAAG | 55819 |
| rs774475507 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930291 | TCGAACTCCTGACCT[C/T]GTGATCTGCCCGCCT | 55819 |
| rs774477221 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056315 | AATGCATACCCTGGG[G/T]CTACATGTGGATGTG | 55819 |
| rs774506207 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023332 | TCTCGGCAGTAACAT[C/G]ACATCTAATGCCCGG | 55819 |
| rs774506964 | in-del | -/AT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043133 | GACTAGCCTGGGCAC[-/AT]AGTAAGACCCTCATC | 55819 |
| rs774515361 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977484 | ATCCCAACACTTTGA[A/G]AGGACAAGGCAGGAG | 55819 |
| rs774538384 | in-del | -/ACTT | 0.000187143 | 0.00967143 | intron-variant | RNF130 | GRCh38.p7 | 5:179920451 | GAAGAAGAGAAAGAG[-/ACTT]AATAGGTCACCAGGC | 55819 |
| rs774563356 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003921 | CTATACTAACTAAGG[A/T]TTATTCGGTACATAC | 55819 |
| rs774584352 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037644 | ACTGAATCAGAATTT[C/G]CATTTTAACAAGATT | 55819 |
| rs774598296 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037534 | TTTCCCTTCTTCACT[A/G]CCTTCTTTCTCAAAT | 55819 |
| rs774616187 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003218 | CTGACATGGAGGCAC[A/G]AAGAGGGGGGTTTGA | 55819 |
| rs774641021 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | RNF130 | GRCh38.p7 | 5:180013179 | AAGACTAGAGAGCCA[C/T]GGCTGAAGTTCTTCG | 55819 |
| rs774644499 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027932 | AAGCACAGCTTAGGC[C/T]GCATCAACCTCATCG | 55819 |
| rs774645048 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931219 | TCTGAACTGGGACTG[-/T]TAACACTGATGGCGA | 55819 |
| rs774651170 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991615 | GATGTTTTTCTTCCA[C/T]TTGATCTAGATCAGT | 55819 |
| rs774712975 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005737 | TCCTTGACTCCCTGA[C/G]AGTAATATCACTCTG | 55819 |
| rs774747246 | in-del | -/G | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954936 | ATCAGTAAAGCAAAA[-/G]TATTTCACCGGCACA | 55819 |
| rs774755559 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180042017 | CACTGAACTCCAGCC[G/T]GGGTGATAGAACAAG | 55819 |
| rs774759688 | snp | C/T | 2.78788e-05 | 0.00373345 | missense | RNF130 | GRCh38.p7 | 5:180071579 | CGGGCTCCTGCACCG[C/T]CACGTTGATGAGCGC | 55819 |
| rs774790192 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070620 | GATAATGGCAGATAT[C/G]TCCCAAAAGTTCAGC | 55819 |
| rs774792003 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001618 | GTCAGCAGGGCTCAG[C/T]GGCAACTTAGGTCCC | 55819 |
| rs774802608 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944097 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 55819 |
| rs774855748 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941068 | TCCACTTATTGGTCA[C/T]TGGTTTCCTGAACAT | 55819 |
| rs774877158 | in-del | -/CA/CGCA | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072931 | AAACGCGCGCGCGCG[-/CA/CGCA]CACACACACACGACT | 55819 |
| rs774883893 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959080 | TGTATGCACTGGTTA[G/T]TCAACATGAGGCTCT | 55819 |
| rs774890039 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971126 | TCTTATTCAGGCAAG[C/T]AGAAAGTCACAGTCT | 55819 |
| rs774901246 | snp | A/T | 1.83731e-05 | 0.00303087 | intron-variant | RNF130 | GRCh38.p7 | 5:180013324 | TGCCTGCAATATAAA[A/T]TAAATATATAACTCA | 55819 |
| rs774966483 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999972 | GGTTTGGCGGTTTAC[-/T]TGTAGTGCTAAGATT | 55819 |
| rs774969649 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060151 | AGAGCTCCAAAGCCA[C/T]GCAGTCTTGCCAACA | 55819 |
| rs774977926 | snp | C/T | 2.50203e-05 | 0.00353688 | intron-variant | RNF130 | GRCh38.p7 | 5:179963439 | CCTGGGATCATCTGG[C/T]ACATGCAATCCAAAA | 55819 |
| rs774979467 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050844 | ACAGGGTTTCACTCT[A/G]TCGCCCAGGGTGGAG | 55819 |
| rs774986272 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999514 | ATCACCTGAGGTCAG[G/T]ATTTCGAGATCAGCC | 55819 |
| rs774987743 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937610 | TTGTTGGCAGGAATG[C/T]AAAATGGTTTAGCCA | 55819 |
| rs774993413 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946911 | CTTTAGCCTCGGGCT[C/G]ATCTCAGGGCCGGTT | 55819 |
| rs774999878 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022331 | ATCAGTACAGATTCA[A/T]GGTTCCTATTTTATT | 55819 |
| rs775000023 | in-del | -/ATA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927342 | TTTGTTATTGGCTAC[-/ATA]ATAATGTTATTAAGT | 55819 |
| rs775021020 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059179 | CACCTTTTAGTCTTC[A/G]TGTATATTTCCTTGG | 55819 |
| rs775025014 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072489 | GACCTGCAGGGACAC[A/G]AGTGGTTGGGAAAGA | 55819 |
| rs775037559 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021958 | TCTGCAACTGTCTCT[C/T]GGTCTTTCTTGGTGT | 55819 |
| rs775084913 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066031 | GTCATCCTAATAATG[-/T]TTAATGTTTTCACTG | 55819 |
| rs775092980 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063994 | ACACAATCACACTGT[A/G]CCCAATTCCATTACC | 55819 |
| rs775094038 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067920 | CATTAAAGGAACCAT[C/T]AAAGGCTTCGTCTAA | 55819 |
| rs775105339 | snp | C/T | 1.65551e-05 | 0.00287702 | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955613 | AATAGGTTCTTTTTT[C/T]CTTCAAGGCAAAATC | 55819 |
| rs775130364 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032045 | AACCTTTTGCCCGTT[G/T]TAAAACTAGGTTGTT | 55819 |
| rs775142908 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981260 | CTAGGAACACTCACA[C/T]TGGGACAAGGGGCAA | 55819 |
| rs775146359 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062968 | AGAAGACATAGAAGC[C/T]CTGGGAACTGAAAGA | 55819 |
| rs775174175 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967014 | TGGCAAATTCGGCTG[C/T]AAAATATTTCCAGGT | 55819 |
| rs775189546 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922400 | TCACTGCAACCTCCA[C/T]CTCCTGGGTTCAAGA | 55819 |
| rs775196915 | snp | A/G | 4.98604e-05 | 0.00499277 | intron-variant | RNF130 | GRCh38.p7 | 5:180040685 | ACATTAAAGATAAAT[A/G]AAACTGACCAAGTCT | 55819 |
| rs775220389 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018784 | CAGCTACAAAAGAAT[G/T]TATGCTTTAGTTTAG | 55819 |
| rs775221725 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070512 | AAATCATGACTTTAT[G/T]TAGGTTGCCTACTTT | 55819 |
| rs775229603 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976861 | TTTAAAGGGAAGGGA[A/G]GAGGAAGAGGCAAAC | 55819 |
| rs775243137 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926194 | AGTGAACTACGTAAA[A/C]TCCAGTCATACAGGC | 55819 |
| rs775273633 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068387 | TCCGTTTCTAAACAC[G/T]AATTCTTTACCAGTT | 55819 |
| rs775302204 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024809 | TCCCACTCCCTTCAC[A/G]AATGAGGGGTCCCTT | 55819 |
| rs775302967 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179952720 | ACCACATTCATAGGA[C/T]AGAATAGAATAAAGG | 55819 |
| rs775321560 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180056797 | CCACAGGCCCATGGA[C/G]AGCAGAATGCATAAC | 55819 |
| rs775338031 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973506 | ACTGGGCCAGGGGCG[C/T]TTAATCTACCTTGGG | 55819 |
| rs775347390 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972353 | TTTTCAGGAGGAGTA[C/T]GGACCTATGCACTGG | 55819 |
| rs775365916 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980397 | AAAGTAAAAAGTGTT[A/G]GAACACCCTGTTAGG | 55819 |
| rs775370972 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055890 | GGAGTTCAAGACCAC[C/T]CTGGCCAACAGGGTG | 55819 |
| rs775373209 | snp | A/G | 1.81204e-05 | 0.00300996 | intron-variant | RNF130 | GRCh38.p7 | 5:179970541 | TATGTCACAAGTTAC[A/G]TACCAAGAAACTTAT | 55819 |
| rs775374033 | snp | A/G | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955477 | AGACTCAACAGCACA[A/G]ACTTTTTATTTTATT | 55819 |
| rs775394157 | snp | A/G | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073734 | CTAGGCCAAAGCAGC[A/G]GGGTCCTCGCCCTGG | 55819 |
| rs775452531 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179941059 | TTTGTTATTTCCACT[C/T]ATTGGTCATTGGTTT | 55819 |
| rs775457828 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954479 | AGACACAAAAGGCCA[C/T]ATATTATATGGTTCT | 55819 |
| rs775485807 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995263 | ACCACAGGAATCAGA[C/T]AGACCATATATCTGC | 55819 |
| rs775485809 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930384 | TAAATTGCTTATTGT[C/T]AGTCTATAGAAATAT | 55819 |
| rs775497356 | snp | C/T | 2.49082e-05 | 0.00352895 | intron-variant | RNF130 | GRCh38.p7 | 5:179966795 | GTGCCTGAGCGGAGG[C/T]CCCCACTTACTTGTT | 55819 |
| rs775534396 | snp | A/G | 3.64677e-05 | 0.00426996 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071556 | AAACGTGAGCGGGGC[A/G]CCGCGGCCGGGCTCC | 55819 |
| rs775534572 | snp | C/T | 1.72976e-05 | 0.00294083 | intron-variant | RNF130 | GRCh38.p7 | 5:179970405 | AAATAAAATAGGAAA[C/T]GTACCACAATTCCCA | 55819 |
| rs775534695 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929535 | GGAGGACTGCTTGAG[A/C]CCAGGAGTTTGAGAC | 55819 |
| rs775548731 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044529 | CAAACGCCTTGCTCT[C/T]GACTCTTAAAGAGCC | 55819 |
| rs775553070 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968318 | AACAAACAAACAAAA[A/G]AAGAAGGCGGCGGCT | 55819 |
| rs775555706 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984061 | TGAAAATGCATTTTT[A/T]AAAACCAATTCAATT | 55819 |
| rs775651867 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979399 | AATTGGTAAAACTTA[-/G]GAAGACAGAGAATCA | 55819 |
| rs775663858 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035596 | ATTACTAAGAGTAGG[G/T]TGTTAAAATCTCCAA | 55819 |
| rs775669965 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047346 | TTCATTCTCTTTATC[C/G]ACTTCCATGGATATA | 55819 |
| rs775701811 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957206 | CACCTGAGGTCAGGA[A/G]TTTGAGACCAGCCTG | 55819 |
| rs775713157 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002797 | ATTCCTCGGATGCAC[C/T]CCTGTACTCTCCCTC | 55819 |
| rs775725140 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180046261 | AACTCCAGGGCCAGC[C/T]TCGGCCAGCCCAGAG | 55819 |
| rs775733822 | in-del | -/TTGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051716 | TATCTCAAATGGATT[-/TTGA]TTATTTTTTACATCC | 55819 |
| rs775749637 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931829 | TAACTGTGATTCAGG[A/C]CCCCCAGCACCCCCG | 55819 |
| rs775750984 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180029421 | AACAGGAGACAATGG[A/G]CAACAGCCTAGAAGT | 55819 |
| rs775763091 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006368 | GTTTTAACCTTTCTC[C/T]GACACAGGAATGTTC | 55819 |
| rs775823324 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995759 | TCCCCATCTCCTGTA[C/T]TGGGGATTTTCTGTT | 55819 |
| rs775854570 | snp | C/G | 0.000540467 | 0.0164299 | missense | RNF130 | GRCh38.p7 | 5:180071672 | CGAGCGCGGCGAGCC[C/G]GGCAGGGCCCGCCCG | 55819 |
| rs775858766 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070443 | TAGCACTTTGGCATA[C/T]AAATACAGACCTCAG | 55819 |
| rs775890460 | snp | C/G | 1.66194e-05 | 0.00288261 | intron-variant | RNF130 | GRCh38.p7 | 5:179978301 | CTAAAATGAAAAGTA[C/G]AGAAACAAAAAGTCA | 55819 |
| rs775947306 | in-del | -/TGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982571 | TGAGATTTTGTGTTT[-/TGTTT]TGTTTTGTTTTGTTT | 55819 |
| rs775980071 | in-del | -/TTTATTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944458 | CTCCAATTTTCTCAA[-/TTTATTT]TTTATTTTTTATTTT | 55819 |
| rs775998455 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977681 | ACATGATGAAACCCC[A/G]TCTCTACTAAAAATA | 55819 |
| rs776020311 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009831 | TTATTTGTAATAGCC[-/A]AAATCTGAAAACATC | 55819 |
| rs776040480 | snp | A/G | 1.65081e-05 | 0.00287293 | missense | RNF130 | GRCh38.p7 | 5:179966869 | CCTGAGGAAGAGGTG[A/G]GATCCCCGAAGTTCG | 55819 |
| rs776058626 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058055 | CACACATTTGGTATC[A/G]GAGTGCTGCAGGTAA | 55819 |
| rs776067858 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982260 | TTATCTAGTATCCCA[C/T]TGAAGAGATGGCCCA | 55819 |
| rs776071209 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040760 | GCACGTGAAGCAGCT[C/T]GCTGCCAGCAGAGCT | 55819 |
| rs776076470 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072840 | GGTTGGGGAGCCCCT[G/T]CTCTAGTGACTAGGT | 55819 |
| rs776094272 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031959 | TCTAGAGGATGTGAA[A/G]TAGTATTGTTTTGGT | 55819 |
| rs776103807 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958972 | AGGTGTTAGCTACCA[C/T]GCCAGGCCACAAAGT | 55819 |
| rs776112188 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069523 | CTGACTTCACACCCA[A/G]TCTTCACACACTGCC | 55819 |
| rs776150954 | snp | A/G | 3.19678e-05 | 0.00399786 | missense | RNF130 | GRCh38.p7 | 5:180071566 | GGGGCGCCGCGGCCG[A/G]GCTCCTGCACCGTCA | 55819 |
| rs776155636 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044470 | ATGAATAGTAACTTA[C/T]GTGCTCAGCTACACG | 55819 |
| rs776170996 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927970 | CTGTCTGACACACAA[A/G]TGTCTGACATTTATG | 55819 |
| rs776177652 | snp | A/G | 7.49372e-05 | 0.0061207 | intron-variant | RNF130 | GRCh38.p7 | 5:180071447 | CGCCGCCCCCGGGCC[A/G]GCACTCACCTCCGTG | 55819 |
| rs776250704 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009973 | AGTATCTTGGCCGGG[C/T]GCAGTGGCTCACGCC | 55819 |
| rs776252308 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986375 | TCATGACTTCTCTCC[A/G]CTTCTTGGGAGCATT | 55819 |
| rs776254124 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991436 | TTTCCTTAAGTAAGT[C/T]TTCTAAACTCCTTGC | 55819 |
| rs776267163 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043564 | TTTCGACAGTGTCAC[A/G]GTCCACTCAGAAGAC | 55819 |
| rs776274773 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999849 | TTAATCTGCTTACAT[G/T]CAAGGTTATTACTGG | 55819 |
| rs776275389 | snp | A/G | 1.83832e-05 | 0.00303171 | intron-variant | RNF130 | GRCh38.p7 | 5:179970549 | AAGTTACATACCAAG[A/G]AACTTATTAGGCCAA | 55819 |
| rs776310560 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024900 | CAGTAAAGCTCTCCT[-/G]GGGGTGTCTGGAAGC | 55819 |
| rs776314692 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073690 | AGAACGGCTTTTACT[G/T]ATTTACTTATCCTCG | 55819 |
| rs776328196 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998640 | ACATGTGGCCAATCT[C/T]GAAGAATATTCTACT | 55819 |
| rs776346695 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031325 | AACCCCAACTCTAGT[A/G]AAAATACAAAAATTA | 55819 |
| rs776392105 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009339 | GGGAGATAATCTCTG[C/T]AAGCCACATATTTGA | 55819 |
| rs776461492 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012346 | TTAGTTTTCTACACA[A/C]AAAGTCTAGGAGAGG | 55819 |
| rs776465217 | snp | C/G | 1.66114e-05 | 0.00288192 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015265 | TTTCCCTTTAGAAAT[C/G]TCTTAAAATGTTGTT | 55819 |
| rs776487712 | snp | A/C | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073035 | AGTGCAGCCGAATTC[A/C]GGAACTTACAGGATC | 55819 |
| rs776500385 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065576 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 55819 |
| rs776520547 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179966152 | ACCGTCCTGAGGCAC[C/T]GCCATCAATACACTC | 55819 |
| rs776552261 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958401 | TTACAGTAGGAAGAT[A/G]GTTTTTAGAAAGTCT | 55819 |
| rs776553470 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022163 | TAGTAAAGTTCACTT[G/T]GATAATTTGGTAAAG | 55819 |
| rs776562277 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057311 | CCCAGCACTTTGGGA[-/G]GCCGAGGCGGGAGGA | 55819 |
| rs776601660 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971294 | GCCAAACAGGGAGAA[A/G]GTGGGTGCCAGGACA | 55819 |
| rs776634092 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958815 | TCTCAGCCTTAGCTG[C/G]GATTACAGGTACCTG | 55819 |
| rs776635527 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968650 | CAGCCTGGGTGACAA[A/T]GGGAGACTCTGTCTC | 55819 |
| rs776640089 | snp | C/T | 1.64988e-05 | 0.00287213 | missense | RNF130 | GRCh38.p7 | 5:179966874 | GGAAGAGGTGAGATC[C/T]CCGAAGTTCGAAGTG | 55819 |
| rs776677820 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000911 | TTACTAGGGAATTAC[A/G]TTCCTTTGATGGTGT | 55819 |
| rs776731082 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066636 | AGGTTGGGAGTTCGA[C/G]ACGAGCCTGATGAAC | 55819 |
| rs776756907 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974855 | GGCGCGGGGAGGAGC[A/G]GCATGGACCGCAGCA | 55819 |
| rs776787223 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981477 | CAAAAGAACAGAGAA[G/T]GATTTAATAAAGCCT | 55819 |
| rs776799670 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058900 | TTTTGCAAGACAAAG[A/G]GTTCTGTAGATGGGT | 55819 |
| rs776799790 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045907 | AGACCCCACCCAACT[C/G]AGGAGCCCAGCTGGC | 55819 |
| rs776799866 | snp | A/G | 1.68335e-05 | 0.00290111 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015351 | ACGGATCCCACAAAC[A/G]ACATATGACAATCAG | 55819 |
| rs776800359 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049036 | TAAGGTTTCTGTTTT[C/G]TGTTTTAAATAAGCA | 55819 |
| rs776808182 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996963 | TTTTCTTTAATGGGA[A/G]ACTTTTAATTACAGA | 55819 |
| rs776813907 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973698 | TGGACACCCAGGAGG[A/C]CTCAGAAAGAGGCAC | 55819 |
| rs776829507 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057270 | ATGTCTGTGTCGGGG[C/T]GGGCACAGTGGCTCA | 55819 |
| rs776830877 | in-del | -/AAAAC | 3.41851e-05 | 0.00413417 | intron-variant | RNF130 | GRCh38.p7 | 5:180040420 | TGATTTCTAAGAAGA[-/AAAAC]AAAATCAACAACCCT | 55819 |
| rs776847794 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179967625 | AATTAAAAAGTGAGC[A/G]CCAAAAGTCTTCCGT | 55819 |
| rs776869467 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180013435 | GGGTATGCAAACTCC[A/C]CTTCTCAACTGAAAT | 55819 |
| rs776872052 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995761 | CCCATCTCCTGTATT[A/G]GGGATTTTCTGTTTT | 55819 |
| rs776880527 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949869 | AGGAGCAATCTGTAA[G/T]CAATCGGATCACTGT | 55819 |
| rs776917296 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964263 | GGCCACCACAGAGCT[A/G]AAAACCTCTGGTGCT | 55819 |
| rs776921653 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026554 | ATGACGTCATGGACA[A/G]GGCACTGGAACAGAC | 55819 |
| rs776923341 | snp | G/T | 3.41939e-05 | 0.0041347 | intron-variant | RNF130 | GRCh38.p7 | 5:180013026 | CTGTGAACTCTGGCT[G/T]TTACGAACCAATCAC | 55819 |
| rs776938888 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020337 | ACGGAGAGGAAGAAC[A/G]CGGTCTGCTGCACAA | 55819 |
| rs776959886 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012980 | TTAAAAGAAAAAACA[C/T]GTTAGTAAGATGCAT | 55819 |
| rs776993916 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon | RNF130 | GRCh38.p7 | 5:179980174 | CAATTTACTGATGGC[C/T]TTCTTGGCTGCATCT | 55819 |
| rs776994171 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062885 | TTTTACAGAACCCAA[A/G]AATTTTTGTAAAGTT | 55819 |
| rs776995151 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044063 | TTAAGTAGTATTACT[A/C]CAAAATTTAATACCA | 55819 |
| rs777016831 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018392 | GAAACTTACAATCAT[A/G]GCAGAAGGCACCTCT | 55819 |
| rs777043091 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976617 | ATAGATTTTCCTTTA[C/T]ATGTAAACTAGAATG | 55819 |
| rs777049384 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954269 | AGAGAACTGAAAATA[-/T]TATGTTCAGGCCAAA | 55819 |
| rs777055704 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006120 | ACTTCTCAGCTCAAA[C/T]ATCTATTTCCCCTTT | 55819 |
| rs777080793 | snp | G/T | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954959 | CCGGCACATGTAAAA[G/T]CGCTCTCACCTACTT | 55819 |
| rs777104937 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068125 | CCCCACCAGCACATC[A/T]GCATACATAATCACA | 55819 |
| rs777131980 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024459 | AGTAAAGTTTTTTTT[C/T]AAAGACTCATTATAT | 55819 |
| rs777149316 | in-del | -/GTG | 2.08775e-05 | 0.00323084 | intron-variant | RNF130 | GRCh38.p7 | 5:179970382 | TAATAATATACAAAA[-/GTG]GTAACAAATAAAATA | 55819 |
| rs777152577 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | RNF130 | GRCh38.p7 | 5:179980149 | CACCCTTCTTTACTG[C/T]CCTGGTTGTCAATTT | 55819 |
| rs777158893 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934692 | AGACCACAGGTGTGC[A/G]CCACCACATCCGGCT | 55819 |
| rs777164293 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179955995 | ACATGTTCTGAATGC[C/T]GAGGGTGCTGAAATC | 55819 |
| rs777191783 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933586 | GAGTGCAGTGGTGCA[A/G]TCATGGCTCACTGCA | 55819 |
| rs777201193 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921266 | GGTGCCTCTCAATCC[C/G]TTGCCCTTCTTTCTA | 55819 |
| rs777223034 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050764 | TAAAAAATTCCAGAC[G/T]GTTAATTTTCTCTCA | 55819 |
| rs777251113 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039045 | TGTTTCCACATAGAT[A/G]TCCAGCTAAATTAAA | 55819 |
| rs777330963 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947680 | GCAGCAAAATGCTTC[-/AA]AGAGGACCTAGCATG | 55819 |
| rs777336731 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179922245 | TAGCCAACCGTGTAT[A/C]TTCGTTTGTGAAGTG | 55819 |
| rs777348771 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942230 | ATTAACCAGCAGTTG[C/T]TATTTCTGTACCATC | 55819 |
| rs777359975 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066512 | TGTCCCTCATGGGTA[C/T]AGTCTAGCAAGTTTG | 55819 |
| rs777393559 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179931447 | TCTTTTTTGTTGGCA[G/T]TAACAGATTTTAATG | 55819 |
| rs777406859 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926992 | CCACTGACTGTTGGT[C/T]ACGGAAGTCTTCTGT | 55819 |
| rs777413526 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025786 | AGGTAGTTAAATCCA[C/T]ATTCAATTAGAAGCT | 55819 |
| rs777414950 | in-del | -/TTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180032216 | TTTGATAAAATCTAA[-/TTTT]TTTTATAAACAGTGT | 55819 |
| rs777441983 | snp | A/G | 4.97352e-05 | 0.00498649 | intron-variant | RNF130 | GRCh38.p7 | 5:179955682 | ACCCTATGGAATAAA[A/G]GGAAAAAAGAGGTCA | 55819 |
| rs777445874 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179980774 | TCCAGGGTTGAGCTG[C/T]TTTCATTATCTGTAA | 55819 |
| rs777448861 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943160 | AGATCGCGCCACTGC[A/G]CTCCAGCCTGGGACA | 55819 |
| rs777452806 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943151 | AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG | 55819 |
| rs777464663 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985349 | ATCTTTCCAGACTTT[C/T]GTGATGTTTTATCTG | 55819 |
| rs777468854 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938462 | TCTTTTTGGGGTGAT[G/T]AAAACGTTTTGGAGC | 55819 |
| rs777474675 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014198 | AGACCTTTCCCCTAC[A/C]TAATTTCCAGAAGTA | 55819 |
| rs777475730 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953940 | AAATGGGTAAAGCAC[C/T]GGGATAGACATTTCT | 55819 |
| rs777500194 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180009914 | CATGGGATATAGTTC[A/G]GCCATAAAAAGGAAT | 55819 |
| rs777502664 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179947981 | TTCACCCTGAGACTC[G/T]GAATTGCTCTAGGGT | 55819 |
| rs777502710 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | RNF130 | GRCh38.p7 | 5:180013095 | TTTGTGTACCTGATC[C/T]TCTGAATGAAGTAGA | 55819 |
| rs777553273 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | RNF130 | GRCh38.p7 | 5:179966917 | GGGAGTTGTCGCCGG[C/T]GAGGTCGCCGAGGGC | 55819 |
| rs777575043 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939953 | TGTCATAAACGTCCC[-/T]TTTTTTTTTTTCTAG | 55819 |
| rs777585477 | snp | A/G | 0.000186445 | 0.00965339 | utr-variant-3-prime | RNF130 | GRCh38.p7 | 5:179920306 | CCCAACAGCCAGGCC[A/G]TGTTTAAAATTCAGG | 55819 |
| rs777596383 | in-del | -/AAAAAAAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055282 | AAAAAAAAAAAAAAC[-/AAAAAAAAA]CAGCAAACAAACAAA | 55819 |
| rs777664446 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | RNF130 | GRCh38.p7 | 5:179980228 | CAAATAAAAACAGAT[A/T]CTAAGTGTAAGATCT | 55819 |
| rs777688869 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047073 | GCTTCCTACAAAAGA[A/G]GTAAAAATAAAAATG | 55819 |
| rs777695040 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060698 | CATAAATACGTAGTC[C/T]TCTGGAGAAAGGTAC | 55819 |
| rs777704397 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003605 | TTCCCATCACTTTGC[A/G]ACAGGTAAACCTGTG | 55819 |
| rs777705050 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933952 | TTTCTAGATCTTTGA[A/G]CTGCACCTCCAAGTT | 55819 |
| rs777717467 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180044826 | GACGGAAGTAGACTC[C/T]GTCTCAAAAAAAAAA | 55819 |
| rs777720835 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036418 | GACTCTGGTGTCATT[C/G]ACCACTGCAAACAGA | 55819 |
| rs777734228 | in-del | -/AAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005434 | CCTCTGTCTCAGAAA[-/AAC]AACAACAACAACACC | 55819 |
| rs777745024 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179954208 | TCAAGAAGTTAAACA[C/T]AGAGTTATAACATAA | 55819 |
| rs777746780 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976451 | GGCAAGTGTGGATGA[C/T]GCCTCCCTGTGTCCC | 55819 |
| rs777758128 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180030748 | CTTTCTGTCTCTGTA[C/T]GTTTGACTTTCTTAG | 55819 |
| rs777792917 | snp | C/T | 8.70189e-05 | 0.0065956 | intron-variant | RNF130 | GRCh38.p7 | 5:179970375 | ATACATATAATAATA[C/T]ACAAAAGTGGTAACA | 55819 |
| rs777812125 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946062 | CCATCAGCGTTTCGC[C/T]GTCCTCCAAGGGACT | 55819 |
| rs777826872 | in-del | -/TG/TGTGTG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937904 | TGCTTTCAATGAATC[-/TG/TGTGTG]TGTGTGTGTGTGTGT | 55819 |
| rs777836624 | snp | C/T | 1.65067e-05 | 0.00287282 | missense | RNF130 | GRCh38.p7 | 5:180040606 | TGATATTAGGAGGGA[C/T]AAAGAACCGGGTTTG | 55819 |
| rs777844463 | snp | A/G | 5.25123e-05 | 0.00512381 | intron-variant | RNF130 | GRCh38.p7 | 5:179970517 | CATGCCTATAAAATA[A/G]TGGAGAATTATGTCA | 55819 |
| rs777854830 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924234 | GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 55819 |
| rs777855536 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977530 | GGAGTTCATGTTCAG[C/T]TGTGCGCAACATAGT | 55819 |
| rs777871784 | snp | A/G | 0.000157816 | 0.00888161 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071538 | GCGCCCGCGGTCGAT[A/G]CGAAACGTGAGCGGG | 55819 |
| rs777903444 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005876 | ATGTGCCAGGCCCCA[C/T]GCTAAACCCCAAGGA | 55819 |
| rs777962054 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937412 | ACAATTCTCCAAAGA[A/G]GATGTATGAGTGGCT | 55819 |
| rs777966769 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063620 | GGTAACAGGAGGTAC[A/G]TGGAGAGAAAACAAT | 55819 |
| rs777993554 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995351 | GCTCCAGTCCCATGA[C/T]GGGGGTGCAGGGGTC | 55819 |
| rs777995379 | in-del | -/G | 1.65704e-05 | 0.00287836 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015313 | TGGTATAAGATACCA[-/G]GTATGGCTATAAAGT | 55819 |
| rs778049478 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977256 | CACAGCAGGCACAAA[-/G]CAGGTATCAGTTCTT | 55819 |
| rs778063838 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929329 | TGTCCATCCTTGCAT[C/T]GATACCTTACTGTCT | 55819 |
| rs778089880 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039736 | TCATGAATGCAAAAC[C/T]AAATTTTATCTGGAT | 55819 |
| rs778093362 | in-del | -/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997426 | CCTCCCAGGTTCAAG[-/C]CATTCTCCTGCCTCA | 55819 |
| rs778134636 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962669 | TTCTATACCTTATCC[C/T]TATGGAAAGCTACTC | 55819 |
| rs778141250 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180051964 | TGTCACAGTGCAATA[C/T]AAGTGTTAATTGTTT | 55819 |
| rs778157254 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179938376 | ATCATGGGGACAGGA[A/C]ACAGATTGGTAGTTG | 55819 |
| rs778163807 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023786 | CCAAATAATTATGTA[A/G]ATACTCTACCCTAAG | 55819 |
| rs778209448 | snp | C/T | 7.26471e-05 | 0.00602647 | intron-variant | RNF130 | GRCh38.p7 | 5:179963614 | GGAGAAGGTTTAAGT[C/T]AAATCGATGCCAACA | 55819 |
| rs778219813 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965936 | CCCAGACTGGAGAAG[A/G]GTCCCACGAGCCTCA | 55819 |
| rs778226224 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973434 | AGGCAAAGTTCTGCT[A/G]CAACAGTCTGGTGCT | 55819 |
| rs778249708 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000369 | ACTGTAATGTGACAC[A/G]GGGAGGATGTTTTCA | 55819 |
| rs778288203 | snp | C/T | 3.57207e-05 | 0.004226 | intron-variant | RNF130 | GRCh38.p7 | 5:180013315 | TATCTCCAGTGCCTG[C/T]AATATAAAATAAATA | 55819 |
| rs778304568 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011075 | TCTTACAAATGCAAG[C/T]AAATCTACATTTTCA | 55819 |
| rs778316389 | in-del | -/GGAAAGGAGTAGGAAAGGAGTAGGGAAAGGAGTAGGGAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015607 | TAGGGAAAGGAGTAG[lengthTooLong]GGAAAGGAGTAGGGA | 55819 |
| rs778342061 | in-del | -/A | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072369 | AACAGACTACAAAGG[-/A]AAAAAAAGCCATAAC | 55819 |
| rs778344074 | snp | A/C | 1.64866e-05 | 0.00287106 | intron-variant | RNF130 | GRCh38.p7 | 5:179980248 | GTGTAAGATCTCTGA[A/C]TGACGTACTTTATTT | 55819 |
| rs778346178 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956089 | TGAAGTGATAGGGAT[G/T]TATGGCTGTCTCACA | 55819 |
| rs778388662 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062671 | TATAAATACCTGAAC[C/G]ATTTTTTTCCAGATG | 55819 |
| rs778395202 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013121 | GTAGAATATGAGCCA[C/T]GCTGAAGAAATAATC | 55819 |
| rs778402591 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950681 | CTTCTTAGCTCTTAA[C/T]AAAAATTCTCTATCT | 55819 |
| rs778417765 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002505 | GGCCACAGGGATTGA[A/G]GCACAGTGTCAGCTC | 55819 |
| rs778450603 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065402 | TGGCTGTGTAACACT[A/C]CACTGAGTGGATATA | 55819 |
| rs778479640 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978644 | AGGTTTCACTGCTAT[A/G]TTTGACACAGCCTGG | 55819 |
| rs778482579 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949728 | CTTTAAGTTATCCTG[A/T]GACTTCAGAGGAATG | 55819 |
| rs778489542 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179953966 | TTTCTCCAAAGAAAA[C/T]AGAAAATGGCCAAAA | 55819 |
| rs778498847 | in-del | -/GCTTCGGA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965335 | GCTACGGTGCCCAGG[-/GCTTCGGA]GCTTCGGAGGGAAAG | 55819 |
| rs778512523 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965305 | ACAGTGGGTGCCAGC[A/G]GGAGGCACTGTGGTT | 55819 |
| rs778516770 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038407 | AAAAAAAAAAGCCTG[-/TT]TTGTTTTTTTTTTTA | 55819 |
| rs778594311 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180066402 | TCTTTTTCTTCCCAG[C/T]CTCAGGTATGTCTTT | 55819 |
| rs778598231 | snp | A/G | | | downstream-variant-500B, intron-variant | RNF130 | GRCh38.p7 | 5:179954848 | TAAGAATTCACTGCT[A/G]CAAACATTTACAAAT | 55819 |
| rs778605324 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929513 | AGCACTTTAGGAGGC[C/T]AAGGTGGGAGGACTG | 55819 |
| rs778616189 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027400 | CTGAGTATAAGCAGA[A/C]ACAGAAAGGCAGAGA | 55819 |
| rs778634564 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976335 | TGGTTTTGGAGGCCC[A/G]TAGTTTTAGGTGCCA | 55819 |
| rs778640506 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959761 | GAGGAGGAAGATCAC[C/T]GGGAGCTTTCTGGTG | 55819 |
| rs778672438 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180037218 | TGTAACACTCTCCTA[C/T]GTGTCGTCCATGCAC | 55819 |
| rs778672485 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022881 | AGAATTTTAAATGGG[C/T]GGGAAAAGAAACATT | 55819 |
| rs778713671 | snp | C/T | | | | | GRCh38.p7 | 5:179919837 | CCCTTCAGCAGGAAG[C/T]AGAATAAGCGAGAGG | 55819 |
| rs778758487 | in-del | -/TTTTTT | | | | | GRCh38.p7 | 5:180033149 | CGGCTACTTTTTTTA[-/TTTTTT]ATTTTTTTGTAGAGA | 55819 |
| rs778759899 | snp | C/G | | | | | GRCh38.p7 | 5:180028606 | GATCCCGCTACGTAG[C/G]TATGCAAAGTTATGC | 55819 |
| rs778788991 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059195 | TGTATATTTCCTTGG[A/C]CTGAAACATCCTCCT | 55819 |
| rs778795527 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998854 | CTCTTTAGATCTAGT[A/G]TTTTTTATATATATA | 55819 |
| rs778806016 | snp | A/G | 1.65847e-05 | 0.0028796 | intron-variant | RNF130 | GRCh38.p7 | 5:179955691 | AATAAAAGGAAAAAA[A/G]AGGTCATAAATTAAA | 55819 |
| rs778840590 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180021132 | CACCAAACCCGGCTC[A/T]TTTTTTTGTATTTTT | 55819 |
| rs778845836 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014135 | CCCACAAGCACAGGC[C/T]ATGCAAGTTAATTAC | 55819 |
| rs778848783 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996682 | TTTTCATCATGAATG[C/T]TCTTTTCAATGTGTT | 55819 |
| rs778887338 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041484 | CGCCTCAATTTTTCA[A/C]TCTGCACATATGGCC | 55819 |
| rs778906013 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043457 | GTTTCTGTGCCAAAA[C/T]ATGTGAGCTACCCCA | 55819 |
| rs778917888 | snp | C/T | 8.13901e-05 | 0.00637875 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180071550 | GATGCGAAACGTGAG[C/T]GGGGCGCCGCGGCCG | 55819 |
| rs778939348 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180020047 | GAAGCTTCAACAAAA[C/T]TAAATGACAGGAAGA | 55819 |
| rs778939872 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180058581 | TTATTTTTGAGATGG[A/G]GTCTTGCTGTGTCGC | 55819 |
| rs778969214 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179987217 | CTGTCACCCAGGCTG[C/G]AGTGTAGTGGTGTGA | 55819 |
| rs778978298 | snp | G/T | 5.29544e-05 | 0.00514533 | intron-variant | RNF130 | GRCh38.p7 | 5:179970525 | TAAAATAATGGAGAA[G/T]TATGTCACAAGTTAC | 55819 |
| rs778980200 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050181 | ACAAAGGGATTTATT[A/G]TAAGGAATTGGCTCT | 55819 |
| rs778996643 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937057 | TTAGCTTTGACACCT[A/G]AAGCATAAGCAACCA | 55819 |
| rs779007400 | snp | A/T | 1.64825e-05 | 0.00287071 | intron-variant | RNF130 | GRCh38.p7 | 5:179978195 | TCAAACAAATGAAGT[A/T]GACATACTTGCAGGG | 55819 |
| rs779011302 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979386 | GTAAAGTCCAAGAAA[C/T]TGGTAAAACTTAGGA | 55819 |
| rs779034214 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974435 | GCCGTGATCACTGAG[A/C]CGAGGAGGAGGCCCC | 55819 |
| rs779037892 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018150 | AAATACAAAAATTAG[C/T]TGGGTGTGGTGGCAG | 55819 |
| rs779051840 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015618 | AGTAGGGAAAGGAGT[-/A]GGGAAAGGAGTAGGG | 55819 |
| rs779096568 | snp | C/G | 1.65712e-05 | 0.00287843 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015314 | GGTATAAGATACCAG[C/G]TATGGCTATAAAGTA | 55819 |
| rs779147970 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061314 | CAGGCACATCCAGAA[A/G]GATGAAGAAAGTATA | 55819 |
| rs779192013 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921873 | TAAAAATACAAAAAA[C/T]TAGCCAGGCATGGTG | 55819 |
| rs779195953 | in-del | -/A | 1.66084e-05 | 0.00288165 | intron-variant, downstream-variant-500B | RNF130, MIR340 | GRCh38.p7 | 5:180015269 | CTTTAGAAATCTCTT[-/A]AAAATGTTGTTCAAC | 55819 |
| rs779199086 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179926505 | ACAAAAAAAATTAGC[C/T]GGGTGTGGTGGCGCA | 55819 |
| rs779208426 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179935192 | ATTGATTTATAACTT[A/G]ATTCCGCTGGTCAGA | 55819 |
| rs779230233 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999579 | ATACAAAAATTAGCC[A/G]GGCTTGGTGGTAGGC | 55819 |
| rs779240530 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180031056 | ACTTCCACTTAATAA[A/G]CAGTAAATATATTTT | 55819 |
| rs779248861 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004671 | TTAAAACAATTCTTA[C/T]GGCTTAATCTAATAG | 55819 |
| rs779255046 | snp | C/T | 5.3241e-05 | 0.00515923 | missense | RNF130 | GRCh38.p7 | 5:180071626 | CTCGCGTTGTCTGCC[C/T]GTGCCGGCCACAGGC | 55819 |
| rs779268072 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027238 | TGTCTTTCCAATTAG[C/T]TTATGTGATTCTGAC | 55819 |
| rs779268565 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179985150 | AAACCCTTTACCCCC[-/T]AACTTTTTTTTTTTT | 55819 |
| rs779268981 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948289 | ATCAGGAGCCCCTGG[C/T]AACAGTTAACAGTTT | 55819 |
| rs779280270 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972112 | AGGCGTTATGTCTTG[C/T]TACTCGTAGCCTCTG | 55819 |
| rs779299056 | in-del | -/TAAGG | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946452 | TTATAAAAAAAACTT[-/TAAGG]TAAAGAAACAAGAGT | 55819 |
| rs779305428 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180054903 | TTACTTTAAATGATA[C/T]TGTGAAATTTTTATT | 55819 |
| rs779306259 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180062348 | TACAGGTGTGAGCCA[C/T]TGAGCCCGGTCCCCC | 55819 |
| rs779326180 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180050475 | ATTCAAACGTTAACC[C/T]CGTCCAAAACCACCC | 55819 |
| rs779339566 | snp | A/G | 3.42161e-05 | 0.00413605 | intron-variant | RNF130 | GRCh38.p7 | 5:180040418 | AATGATTTCTAAGAA[A/G]AAAAACAAAATCAAC | 55819 |
| rs779354267 | snp | C/T | | | synonymous-codon | RNF130 | GRCh38.p7 | 5:179970428 | AATTCCCAGGGCCTT[C/T]AATATATTAAGTTTG | 55819 |
| rs779355000 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179973162 | CCTGTCTTTCCAAAT[C/T]CCCCGCTAGTCCAGC | 55819 |
| rs779366109 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979829 | AAATAAAACAACAAA[A/G]GAGACATAGCAAAGT | 55819 |
| rs779393615 | snp | A/G | 1.67133e-05 | 0.00289074 | synonymous-codon | RNF130 | GRCh38.p7 | 5:180013292 | TTCTGTTATCATGAC[A/G]GCAATAATATCTCCA | 55819 |
| rs779395313 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180043074 | TGTAATCCCAACACT[C/T]TGGGAGGCCAAGGTG | 55819 |
| rs779423848 | snp | C/G | 1.65181e-05 | 0.00287381 | missense | RNF130 | GRCh38.p7 | 5:179966865 | CCATCCTGAGGAAGA[C/G]GTGAGATCCCCGAAG | 55819 |
| rs779461072 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180052124 | CACTGCTAGACCCTC[A/G]CCAAGGTCTGTCCCA | 55819 |
| rs779461579 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983180 | TTAATCATTTTTTCA[C/T]TGGTAGACTGTGCTC | 55819 |
| rs779470960 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023937 | CAGCCAGGTGACCAA[A/C]GTCAACATCACTGGT | 55819 |
| rs779526346 | in-del | -/TAAA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055531 | GTATACCAGTTGTCC[-/TAAA]TAAAGAGAGGGATTT | 55819 |
| rs779539604 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014082 | GACCAGTTTGGCATC[A/G]AAATACCTCCAGCCT | 55819 |
| rs779544368 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179962556 | TTCATCTCTAATTAG[C/T]TTTCATGAATATTGG | 55819 |
| rs779581441 | snp | A/G | 1.66076e-05 | 0.00288158 | intron-variant | RNF130 | GRCh38.p7 | 5:179955707 | AGGTCATAAATTAAA[A/G]AGTAGTCAAATGTTT | 55819 |
| rs779588841 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012946 | TATTAAAATGACTGA[A/G]TGAGGGTAACAACAT | 55819 |
| rs779645316 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974036 | AGAGTGCTGCGGGAG[A/G]GGAGGCCTCTATATT | 55819 |
| rs779649490 | in-del | -/AA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974709 | AGGGCGATGGCTTTG[-/AA]AGAGAGTTTTAAAAA | 55819 |
| rs779659077 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930251 | TTAGTAGAGATGGGG[C/T]TTCACCACGTTGGTC | 55819 |
| rs779700545 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180002196 | CACTGGGGAGGCATG[A/G]TTGCTCTGAGTGTTC | 55819 |
| rs779721421 | snp | A/G | 0.00214133 | 0.0326508 | utr-variant-5-prime | RNF130 | GRCh38.p7 | 5:180071713 | CTCATCGTCCCTCCG[A/G]CAGCCGCCGCTGCTC | 55819 |
| rs779723275 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179991582 | ATTCATCCAAAACAC[-/TT]TTGTCGTCAAGTTGT | 55819 |
| rs779738073 | snp | A/C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968235 | AGGAGGCGGAGCTTG[A/C/T]GGTGAGCCGAGATCG | 55819 |
| rs779777810 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045518 | AAGCTCCCACAGCGC[A/G]GAAGTGGACCTCTGC | 55819 |
| rs779780856 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038537 | GACCCAAAAATGTTA[A/G]TAAGTCCTAGGAGCC | 55819 |
| rs779816156 | in-del | -/TTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179960275 | GCATTTATTCACTTC[-/TTT]GACTACCATCCTGTT | 55819 |
| rs779818873 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180016202 | ACAGAATCTGGCGAA[A/C]GTTATATAGGAGTCC | 55819 |
| rs779836228 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070166 | AGTCTGGCAACACTG[C/T]GCATCTCAACCACAG | 55819 |
| rs779855755 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930869 | CATAACAAAACCCGG[C/T]CTCTACTAAAATTAC | 55819 |
| rs779871794 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014332 | CAGAGAAACTTCTAT[C/G]AATCTATCAGCGATT | 55819 |
| rs779885149 | in-del | -/T | 3.72464e-05 | 0.0043153 | intron-variant | RNF130 | GRCh38.p7 | 5:180013332 | TATAAAATAAATATA[-/T]TAACTCAAGTGACAT | 55819 |
| rs779926548 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179978638 | CTGAAGAGGTTTCAC[C/T]GCTATGTTTGACACA | 55819 |
| rs779928590 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027288 | TGTAGACAGCACTGC[C/G]CTACAGGGTGAGAAG | 55819 |
| rs779943315 | snp | C/G | 0.000168265 | 0.00917084 | missense | RNF130 | GRCh38.p7 | 5:180071634 | GTCTGCCCGTGCCGG[C/G]CACAGGCTGCAGGTC | 55819 |
| rs779965897 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995271 | AATCAGACAGACCAT[A/G]TATCTGCCTTCAGCC | 55819 |
| rs779981858 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026211 | TTGGTTACATGTTTA[C/T]CTAAATTACCTCATC | 55819 |
| rs780017222 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005696 | AATTCAGCTCCAAGG[C/T]CACAACCTACCTTCT | 55819 |
| rs780019819 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057725 | ATGTACCTCTCCATC[A/C]GGCTCTTAATTTGTA | 55819 |
| rs780052419 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039641 | GTGGGCAAGTCTTTG[C/T]AAGAAACTTGCTAAA | 55819 |
| rs780074734 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180068804 | AAAACAAATTTTCAT[A/G]AATTTCACGTATTGG | 55819 |
| rs780077814 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180059297 | CTTGACCACCCTAGA[C/T]TGAGTCTCTTCTGCC | 55819 |
| rs780112885 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179949460 | AGATGGGGTCTTGCT[A/G]TGTTGCCCAGGCTGA | 55819 |
| rs780117166 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180060807 | CTATGTTCGGCCGGG[C/T]GCCTGTAATCCCAGC | 55819 |
| rs780123315 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045213 | CAGGTAAGAATAGTA[G/T]GTAAATATTTAAAGG | 55819 |
| rs780123605 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180036745 | TTTAATCCTACCTTA[C/T]AAATATTTCACAAAG | 55819 |
| rs780132552 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998028 | TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT | 55819 |
| rs780172218 | snp | G/T | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180073218 | GAGGCACTGTTTCCA[G/T]GAAAGGGTACGGATG | 55819 |
| rs780221991 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179934129 | CTAATAAGAACCTGG[C/T]GTTTGCCTCTCCTTT | 55819 |
| rs780228322 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179927128 | ATACCAAATCTTTGG[C/T]AATAAGAAAATGGGT | 55819 |
| rs780243355 | snp | A/G | 8.32106e-05 | 0.00644968 | intron-variant, nc-transcript-variant | RNF130, MIR340 | GRCh38.p7 | 5:180015338 | TAAAGTAACTGAGAC[A/G]GATCCCACAAACGAC | 55819 |
| rs780271272 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180022742 | ACTAGTTTTAAACAA[C/G]CCATTTGCAGGTTGA | 55819 |
| rs780301133 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179986843 | TTCTGTGATCTCTTC[A/C]ATTTCTTTCATCAGT | 55819 |
| rs780301762 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971865 | CAACTTTGGCCTGAA[C/T]AATATACACACACGT | 55819 |
| rs780330084 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179965932 | GACTCCCAGACTGGA[A/G]AAGGGTCCCACGAGC | 55819 |
| rs780361614 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008772 | GCCTGTAATCGCAGC[C/T]ACTCGGGAGGCAGAG | 55819 |
| rs780381588 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179964002 | AAGGCTGAGGAGCAC[A/G]GAGCAGCAGTTCTCC | 55819 |
| rs780458487 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065302 | TCGATATAACACAAC[A/C]ATTTTTATGTCTGCA | 55819 |
| rs780476475 | snp | C/T | 1.65745e-05 | 0.00287871 | intron-variant | RNF130 | GRCh38.p7 | 5:179967036 | TTTCCAGGTTAAAAA[C/T]AATTGTAAGGAAAAC | 55819 |
| rs780489021 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179948927 | GACGTTCTTATCAAC[C/T]TCTGACCAACCTGGC | 55819 |
| rs780504999 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179951152 | TAACCAGTGCAGCTT[G/T]AAAACATTCTTCAAC | 55819 |
| rs780544291 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053335 | GAACAGAAGTGACAA[A/G]TCACATGGAAGAAAG | 55819 |
| rs780551662 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981874 | TTTAAACCACCTTAT[A/G]GAGATATAATTGACT | 55819 |
| rs780559763 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011278 | CTATAAAGGTCATTA[C/T]TGAGCCAGTTTTACA | 55819 |
| rs780606237 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180035876 | AATTTTTATGTTCTT[A/T]ACTGAGAATCTCTAT | 55819 |
| rs780614721 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180026001 | TTTTCTATATTTTAC[A/C]AAGTGTGACATTTTT | 55819 |
| rs780621605 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924657 | AGCCAGGCATGGTGG[C/G]GGGTGCCTGTAATCC | 55819 |
| rs780675191 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027133 | GGAGGGCAAAACTGG[C/T]ACAGGAGCAGGACGG | 55819 |
| rs780723418 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179929434 | TCTTGTTATTCTTAG[C/T]TCTTTCCATTTCCAC | 55819 |
| rs780745425 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179979585 | TGTGTCCTTCTAGCG[A/G]AGAAGCAGGGCTCTA | 55819 |
| rs780812710 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179943255 | TGACCAATAGGTGAC[C/T]GGTTTTATGACTGTG | 55819 |
| rs780837977 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180012722 | AGTCTCCCTAACCCC[C/G]CTCCAAGTTCCCATT | 55819 |
| rs780864341 | snp | A/G | 3.29484e-05 | 0.00405871 | intron-variant | RNF130 | GRCh38.p7 | 5:179980219 | TGAAAATTGCAAATA[A/G]AAACAGATACTAAGT | 55819 |
| rs780869170 | in-del | -/CAATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179984067 | TGCATTTTTTAAAAC[-/CAATT]CAATTATTCATTACT | 55819 |
| rs780885461 | snp | C/G | 2.14172e-05 | 0.00327233 | intron-variant | RNF130 | GRCh38.p7 | 5:179963599 | AGGAAATCACTCTGG[C/G]GAGAAGGTTTAAGTC | 55819 |
| rs780895641 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179930209 | ATTACAGGCATCTGC[A/C]ACCACACCCGGCTAA | 55819 |
| rs780896362 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179974275 | TGGCATGGAAACATA[C/T]GTTCATCCACGCGGC | 55819 |
| rs780930955 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180000651 | AAGTTGAGAGATTCT[G/T]TCTTACATATGATCA | 55819 |
| rs780949449 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179972805 | TTTAAAGCTGCATGA[A/G]TACAGTGTTCTCTGC | 55819 |
| rs780983203 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179976316 | CTAGTAATATACCCA[C/T]GAATGGTTTTGGAGG | 55819 |
| rs781002871 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179994410 | TGGTTTGTAGTTCTT[C/T]TTGAAGAGGTCCTTC | 55819 |
| rs781003753 | snp | C/T | 6.59011e-05 | 0.00573988 | intron-variant | RNF130 | GRCh38.p7 | 5:179980124 | AAGTTGTTTCATGAC[C/T]GTACCTTGTCACCCT | 55819 |
| rs781080074 | in-del | -/AAAC | | | intron-variant | RNF130 | GRCh38.p7 | 5:179968301 | TGTCTCAAAACAAAC[-/AAAC]AAACAAACAAACAAA | 55819 |
| rs781108696 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179921535 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 55819 |
| rs781130320 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179992371 | TGAGTCTCGATCTCC[A/T]GACCTCGTGATCCAC | 55819 |
| rs781133316 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180004406 | TACAAAGGAGAAAAA[A/C]CAAGCCCCAGAAAGA | 55819 |
| rs781143001 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180024695 | AAGGGAAATGACACC[A/T]AACGGAAACTTGGAA | 55819 |
| rs781160176 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179969351 | CTGCCTGCCTTCTCT[A/G]CTTGCAACTTACCAA | 55819 |
| rs781165559 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180014759 | GGGAAGCCAGGGCAG[A/G]TGGATTGCTTGAGCT | 55819 |
| rs781184925 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180017976 | ACACTGTTACAAATA[A/C]ATACCTGAGACTGGG | 55819 |
| rs781193768 | in-del | -/TATTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999004 | TCTTTTATTTTTCAA[-/TATTT]TATTTTATTTTGTTA | 55819 |
| rs781202858 | snp | C/T | 1.66565e-05 | 0.00288583 | intron-variant | RNF130 | GRCh38.p7 | 5:180040446 | AACAACCCTCATTTT[C/T]GTTTACCTGGATGAG | 55819 |
| rs781204690 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179981611 | CATCACATAATTTCA[C/G]CCATAAAATTTTCAC | 55819 |
| rs781204698 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180049603 | TTTTAAATACTTTGA[A/T]ACATTGTTTCAGTAT | 55819 |
| rs781215176 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180008588 | TCAGTAACACTAAGA[C/T]AATAGTAAAATCTTG | 55819 |
| rs781222838 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039392 | CAGGTACCCTCCACC[A/G]TGCCCAGCTAATTTT | 55819 |
| rs781246288 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180067824 | GAATTCAAACATTAC[A/G]TGACCCCTTTCACCC | 55819 |
| rs781248636 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956468 | CCTTCATGCCCTACC[A/G]CAGCAAGCAACTTCG | 55819 |
| rs781254896 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179942330 | AGGACTGATTCAATA[C/T]ACAATGCATTTATCA | 55819 |
| rs781258036 | snp | C/G | 1.64982e-05 | 0.00287208 | missense | RNF130 | GRCh38.p7 | 5:180040600 | ACTGTTTGATATTAG[C/G]AGGGACAAAGAACCG | 55819 |
| rs781268475 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180007344 | AGGCAGAGGTTGCAG[C/T]GAGCCAAGATCGCGC | 55819 |
| rs781271993 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179970862 | GCTAACATAGAAAAA[C/T]GGAGTTTCAAAAAGA | 55819 |
| rs781297809 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179996685 | TCATCATGAATGCTC[C/T]TTTCAATGTGTTGCT | 55819 |
| rs781323259 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179997908 | GTACAGTGGTGTGAT[A/C]TCGGCTCACTGCAAC | 55819 |
| rs781342045 | snp | A/T | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955249 | CTTGAAGAATGAGTA[A/T]ATCAACTGACCATCC | 55819 |
| rs781369399 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179946139 | CAAGCTCCTAGGGTG[A/C]AACCCCCTACAGTTA | 55819 |
| rs781376566 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179924388 | TAATCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 55819 |
| rs781396581 | in-del | -/ATT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038819 | TGTAAGTAAAACAAC[-/ATT]AATAAGAAAGAAAAA | 55819 |
| rs781401872 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180023248 | ATAGATATGTAGATA[C/T]GCAGGAGTTAGGATA | 55819 |
| rs781403928 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:180053167 | TTTTAACAGATCTCA[A/C]AACTGGCAGACAGGA | 55819 |
| rs781499711 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070410 | CCCAGCCAGACTGTC[C/T]CAAAGAAGAAAACAG | 55819 |
| rs781528651 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179983915 | GAAAATGGGATTTCT[C/T]AAAATTTAACTTTCT | 55819 |
| rs781543111 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179959999 | GATACCTAGTCACGC[C/T]TCCCACTAAACTTCA | 55819 |
| rs781551151 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179950911 | AAGGAAGAATTGCTT[C/T]GATCTCCACTGAGAT | 55819 |
| rs781567333 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179971429 | GGCTGAAGTGCAGTC[A/G]TGCAATCTCTGCTCA | 55819 |
| rs781582809 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180063809 | CCAACGGTACATGGT[C/T]CATCCACAATGGAAA | 55819 |
| rs781599363 | in-del | -/TAACA | | | intron-variant | RNF130 | GRCh38.p7 | 5:180047400 | ACTTTCACTTAAACC[-/TAACA]TTTCTTTTTATTACT | 55819 |
| rs781639833 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001425 | GGCAAAGTGGGATAT[A/G]TTACCCACATGGTCA | 55819 |
| rs781642661 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180069616 | ACAAATCTCCTCTTT[C/T]CAGAATTAAGGAACC | 55819 |
| rs781657961 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant | RNF130 | GRCh38.p7 | 5:179967051 | TAATTGTAAGGAAAA[C/T]ACAACCTTTCATAAG | 55819 |
| rs781677495 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180005246 | CAGCCTGGCCAACAT[A/G]GCGAAACCCCGTCTC | 55819 |
| rs781710240 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064830 | AACTACAGATTAGTT[C/T]TAAGCAGTGAAAACC | 55819 |
| rs781752826 | snp | A/C | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937529 | ATTAGAAATGGCTAT[A/C]ATTTTAAAAAAGGAG | 55819 |
| rs781777807 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180011371 | ATAACCACACTATGG[-/T]TATGTAAGAGAATGT | 55819 |
| rs781780017 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990336 | GAGAGGACAGCTTAC[A/G]TCATCATTTCTTCTA | 55819 |
| rs796067148 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034105 | ATGCTTTTTTTTTTT[A/T]AAATCATGATGGGTA | 55819 |
| rs796097120 | in-del | -/TG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038410 | AAAAAAAGCCTGTTT[-/TG]TTTTTTTTTTTATTT | 55819 |
| rs796114292 | in-del | -/TC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180061065 | GACAGCGAGACTCCG[-/TC]TCAAAAAAAAAAAAA | 55819 |
| rs796123669 | in-del | -/CG | | | upstream-variant-2KB | RNF130 | GRCh38.p7 | 5:180072920 | CTCCACCTTCCGAAA[-/CG]CGCGCGCGCGCACAC | 55819 |
| rs796137614 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179999273 | GTGATCACCTGCCTC[A/G]GCCTCCCGAAGTGCT | 55819 |
| rs796153213 | in-del | -/CA | | | utr-variant-3-prime, intron-variant | RNF130 | GRCh38.p7 | 5:179955216 | CAGAGAAGAAATTAT[-/CA]CAGAGTGAATGTCCC | 55819 |
| rs796174114 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933234 | ATCATCTAGGCCCAG[A/G]GTTTTTCTTTGAGGA | 55819 |
| rs796191775 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180003944 | GTACATACCATGTGC[C/T]AGGTACTGTTCTAAG | 55819 |
| rs796209220 | in-del | -/CC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180070982 | CATTTTCCATTTACA[-/CC]CCCCCCCCAATTTAC | 55819 |
| rs796227222 | in-del | -/AT | | | intron-variant | RNF130 | GRCh38.p7 | 5:180065811 | CAAACACAGAAAAAA[-/AT]GTTTCCTTCCTTTAT | 55819 |
| rs796271207 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180025552 | AAAATGGAACCATTG[C/T]ATTTATTTTATTAAA | 55819 |
| rs796316914 | snp | A/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179977441 | AGGAATCACAAAACA[A/T]TGCCAAGCACAGTGA | 55819 |
| rs796329418 | in-del | -/CT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179995202 | CAGTATGGGACCTGC[-/CT]CTCTCTCTCTCTCCA | 55819 |
| rs796349972 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179963081 | GGGCTTCCCCAGAAG[C/T]TAGACATGCCAGGCT | 55819 |
| rs796350362 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180034203 | TTGATTTTCAGATGT[-/A]AAAAAAAAAAACCAT | 55819 |
| rs796376048 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180006597 | GGGAAGTTTTAAGAA[C/T]ACATTCTAAATATTC | 55819 |
| rs796376765 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179945501 | CTTTCACACACACCA[G/T]GTTTCCAATCCTCAC | 55819 |
| rs796394311 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179961112 | TTCATGCTTACTGTT[-/A]AAAAAAAAAAACACA | 55819 |
| rs796395952 | in-del | -/TT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933400 | TCATAACCCTATTTG[-/TT]TGTGTGTGTGTGTGT | 55819 |
| rs796399366 | in-del | -/TATGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179998882 | ATATATATATATATA[-/TATGTTT]TATATATCTGAGTGC | 55819 |
| rs796422733 | in-del | -/TA | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920780 | CTGGGCATATATATT[-/TA]TATATATATATATAT | 55819 |
| rs796440716 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180040380 | CATGGCTTCAGCAGA[A/G]GCAGAATGCTTACCT | 55819 |
| rs796456635 | in-del | -/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179944158 | ATTTTTAGTAGAGAC[-/G]GGGGGGTTCACCATA | 55819 |
| rs796463176 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180001451 | GGTCAGGATCTGTGA[C/T]TGTCAGGTACCCACT | 55819 |
| rs796472196 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957247 | CAAAACCCCATCTCT[A/G]CTAAAAATGCAAAAA | 55819 |
| rs796476081 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180039774 | TAAGGAGACAGAGTG[A/G]TGAAACTAACAGAAC | 55819 |
| rs796536356 | in-del | -/TGTTT | | | intron-variant | RNF130 | GRCh38.p7 | 5:179982567 | TATGGTGAGATTTTG[-/TGTTT]TGTTTTGTTTTGTTT | 55819 |
| rs796608797 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180027146 | GGCACAGGAGCAGGA[C/T]GGGGTGAAAGCACGG | 55819 |
| rs796609678 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179933402 | CATAACCCTATTTGT[G/T]TGTGTGTGTGTGTGT | 55819 |
| rs796636977 | snp | C/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179937972 | AGAGAGAGAGAGAGA[C/G]AGAGACAGACAGGGT | 55819 |
| rs796667044 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057547 | GCGAAACTCAGTCTC[-/A]AAAAAAAAAAAATCA | 55819 |
| rs796714012 | in-del | -/AAG | | | intron-variant | RNF130 | GRCh38.p7 | 5:180041530 | TCCTCTGCAAATCTT[-/AAG]AAGAAGCCCCCGGCT | 55819 |
| rs796743245 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038105 | GTTGTCCAGGACGCA[A/G]TGCAGTGGTGTGATC | 55819 |
| rs796750025 | in-del | -/AAAGGAGTAGGG | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015445 | AAGACTCAAGCTGGA[-/AAAGGAGTAGGG]AAAGGAGTAGGGAAA | 55819 |
| rs796750193 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179957285 | GGGGTGCTGGCAGGC[A/G]CCTCTAGTCCCAGCT | 55819 |
| rs796776443 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179990160 | AAGATGCGGAGACCA[A/G]TAGTGGCCCCGAATG | 55819 |
| rs796785074 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179956996 | CTGTACCTTATTATT[C/T]CTTGTAGTTCCTATT | 55819 |
| rs796800011 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:179939284 | TTAAGACAGAAAAAA[-/A]GTGGTCCTATTATGT | 55819 |
| rs796805972 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179958068 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTTTT | 55819 |
| rs796824680 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180064964 | GCTCAAAATTATGAC[A/G]TATTTTAGCTTGCTT | 55819 |
| rs796855543 | in-del | -/GGAAAGGAGTAGGAAAGGAGTAGGAAAGGAGTA | | | intron-variant, upstream-variant-2KB | RNF130, MIR340 | GRCh38.p7 | 5:180015455 | CTGGAAAAGGAGTAG[lengthTooLong]GGAAAGGAGTAGGGA | 55819 |
| rs796886409 | snp | G/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:179936447 | TTGCCCAGGCTTGTC[G/T]TGAACGCCTGAGCTC | 55819 |
| rs796897069 | snp | C/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180057912 | CCCACTACCTACAAC[C/T]GGTGTCTGAAGTAGG | 55819 |
| rs796912321 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:179920829 | AGTTTTGCTTTTGTT[A/G]CCCAGACTGGAGTGC | 55819 |
| rs796969281 | in-del | -/A | | | intron-variant | RNF130 | GRCh38.p7 | 5:180018308 | TCAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 55819 |
| rs796970999 | in-del | -/T | | | intron-variant | RNF130 | GRCh38.p7 | 5:180038411 | AAAAAGCCTGTTTTG[-/T]TTTTTTTTTTTATTT | 55819 |
| rs796982793 | in-del | CT/TGTGTGTGTGTGC | | | intron-variant | RNF130 | GRCh38.p7 | 5:180055441 | ATGTCAGATGACTTT[CT/TGTGTGTGTGTGC]TGTGTGTGTGTGTGT | 55819 |
| rs796985356 | snp | A/G | | | intron-variant | RNF130 | GRCh38.p7 | 5:180045448 | CAGCTCATAAAGACC[A/G]CAGGGACCCAAACAG | 55819 |