SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs725303 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RNF2 | GRCh38.p7 | 1:185054536 | CTTCTCCATTACGAG[C/T]GCTCTTCCTGAGAGC | 6045 |
rs1008502 | snp | C/G | 0.245346 | 0.249957 | intron-variant | RNF2 | GRCh38.p7 | 1:185049554 | GAAGCAACAAGATAT[C/G]TGAGAGCAGTTAGAA | 6045 |
rs1046592 | snp | A/G | 0.311369 | 0.242351 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100429 | TTTCTGAGCCAGACT[A/G]GTTTACGCTATTCAA | 6045 |
rs1884447 | snp | A/G | 0.499846 | 0.00878459 | intron-variant | RNF2 | GRCh38.p7 | 1:185052278 | Aacacacaggttcct[A/G]gcaccgctattcatg | 6045 |
rs2057222 | snp | C/T | 0.499693 | 0.0123764 | intron-variant | RNF2 | GRCh38.p7 | 1:185098673 | tctccagcacactgc[C/T]tgctgttgagtacag | 6045 |
rs2144664 | snp | A/G | 0.102014 | 0.201495 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044217 | AGTTATAGATAGTAG[A/G]CAAAAGCTTTCAAGC | 6045 |
rs2281482 | snp | A/G | 0.0248432 | 0.108648 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045588 | GCCGGCGTCCGCGGC[A/G]GCTGATACCAGAGTC | 6045 |
rs2378957 | snp | A/G | 0.405429 | 0.195811 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070933 | TGAGCCACTGCACCC[A/G]GCCAGACTGCAGTAT | 6045 |
rs2378958 | snp | G/T | 0.277867 | 0.248442 | intron-variant | RNF2 | GRCh38.p7 | 1:185073268 | CCCTGTGTGAGAATT[G/T]GTGCTGGGTAAATTT | 6045 |
rs3036553 | in-del | -/TTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082364 | TTTTTTTTTTTTTTT[-/TTTT]GAAGACAGAGTCTTG | 6045 |
rs3753570 | snp | G/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185067036 | CTCCATTATCCGGTC[G/T]TAAGTTTTTGAATAC | 6045 |
rs3753571 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | RNF2 | GRCh38.p7 | 1:185048475 | TATGATAAATGGCAA[A/C]CATGTTAATTCTCAA | 6045 |
rs3753572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185047471 | CACAGACGTGACACC[A/G]CAAACTGTAGGTCAC | 6045 |
rs3753573 | snp | C/T | 0.0513262 | 0.151752 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044870 | CCCCTTCCAGTGTTA[C/T]CTTCTGAACTTGAGG | 6045 |
rs3766720 | snp | G/T | 0.244205 | 0.249933 | intron-variant | RNF2 | GRCh38.p7 | 1:185086134 | GTTAAGGAGGCTTTG[G/T]TAGAGATGAAATAAA | 6045 |
rs3766721 | snp | C/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185054240 | AAAAAGAATGAATGA[C/T]AATGTCCAGTTTAGT | 6045 |
rs3766723 | snp | G/T | 0.267636 | 0.249377 | intron-variant | RNF2 | GRCh38.p7 | 1:185046402 | GGCTCCCGGCAAAAG[G/T]GGGTACTAGCATCTC | 6045 |
rs3820183 | snp | C/G | 0.407502 | 0.194147 | intron-variant | RNF2 | GRCh38.p7 | 1:185067375 | ATTTACTCAAGACTA[C/G]GCAAATAATAAATTG | 6045 |
rs3820184 | snp | C/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185053946 | CTGCTACATTCAATC[C/T]GGGTTACTAACATCC | 6045 |
rs3835513 | in-del | -/TT | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185062477 | AGTTTCCCAACATCA[-/TT]GTTTAGTTCTCTCTT | 6045 |
rs3841690 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099490 | GTTCCTTTTTTTCCC[-/C]TTAGTACTTTGTGTA | 6045 |
rs4651247 | snp | A/G | 0.405603 | 0.195673 | intron-variant | RNF2 | GRCh38.p7 | 1:185079623 | tgttgtccaattcca[A/G]gagcccaaataaaag | 6045 |
rs5779238 | in-del | -/C | 0 | 0 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045374 | GCGGCGCACCCTCCC[-/C]TCGCGCCGCGGGCCT | 6045 |
rs5779240 | in-del | -/T | 0.499087 | 0.0213463 | intron-variant | RNF2 | GRCh38.p7 | 1:185073060 | TGCTCTACGACTTGC[-/T]TTTTTTTTTTTTTTT | 6045 |
rs6674345 | snp | G/T | 0.00835141 | 0.0640778 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102002 | TGATAAAACTGCTTA[G/T]ATTTTGTTGATGACA | 6045 |
rs6677056 | snp | A/G | 0.417521 | 0.185571 | intron-variant | RNF2 | GRCh38.p7 | 1:185085555 | TACAGGTTTTTAACA[A/G]CTTTCTCTCACTGAT | 6045 |
rs6679466 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | RNF2 | GRCh38.p7 | 1:185061372 | ATCTCTTAAAAGGGG[A/G]AAAAAAAAGGGAAAC | 6045 |
rs6684195 | snp | A/G | 0.42263 | 0.180829 | intron-variant | RNF2 | GRCh38.p7 | 1:185057681 | TTTTAGGTAGTGCAG[A/G]GCATATGTTCTTGAC | 6045 |
rs7519019 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | RNF2 | GRCh38.p7 | 1:185068972 | TTGCTCAAAATGTTA[C/T]ATTTAAAGTTCCTTT | 6045 |
rs7541639 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RNF2 | GRCh38.p7 | 1:185076206 | TATGAACCTTTCAGT[C/T]TTCTGGGTATTGTAT | 6045 |
rs7541641 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RNF2 | GRCh38.p7 | 1:185076209 | GAACCTTTCAGTCTT[C/T]TGGGTATTGTATCTT | 6045 |
rs9628633 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075583 | gtacaggaagcatgg[C/T]tgggggaggcctcag | 6045 |
rs10911671 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | RNF2 | GRCh38.p7 | 1:185054915 | atgttgcccaggctg[A/G]tctggaactcctgag | 6045 |
rs10911672 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185055309 | tctttttagcatgat[C/T]ttttgagcatcatgt | 6045 |
rs10911673 | snp | C/G | 0.309154 | 0.242901 | intron-variant | RNF2 | GRCh38.p7 | 1:185065370 | agctggccaccgaag[C/G]ccccagtggcagcct | 6045 |
rs10911674 | snp | G/T | 0.278399 | 0.248382 | intron-variant | RNF2 | GRCh38.p7 | 1:185077442 | TAACATTGATTGTTT[G/T]GGGACTTCCGGTAGA | 6045 |
rs10911675 | snp | A/G | 0.401747 | 0.198678 | intron-variant | RNF2 | GRCh38.p7 | 1:185079943 | CAGAAAAAAAAAAAA[A/G]CCAATTGTGTCTTTA | 6045 |
rs10911676 | snp | C/T | 0.321769 | 0.239477 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102699 | TATTTTCAAGGTTCA[C/T]GTGATAGCATATATC | 6045 |
rs11334881 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081396 | GCCTAATTCCATCAA[-/T]TTTTTTTTTTTTTTG | 6045 |
rs11432393 | in-del | -/T | 0.375 | 0.216506 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100543 | CTGAAGTTTCTTGTG[-/T]TTTTTTTTTTTCCCC | 6045 |
rs11808499 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185085539 | CACATAGTTAATATC[A/G]TACAGGTTTTTAACA | 6045 |
rs12030761 | snp | A/G | 0.278664 | 0.248351 | intron-variant | RNF2 | GRCh38.p7 | 1:185061253 | ctgcctcagcctccc[A/G]agtagctgggactac | 6045 |
rs12038919 | snp | A/G | 0.2776 | 0.248472 | intron-variant | RNF2 | GRCh38.p7 | 1:185072498 | AGATAAAGAATTACA[A/G]GGTTAGAATTTCTTT | 6045 |
rs12038977 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | RNF2 | GRCh38.p7 | 1:185072685 | ACAGCTCATGCCTGT[A/G]ATCCCAGCACTTTGG | 6045 |
rs12039657 | snp | A/T | 0.277067 | 0.24853 | intron-variant | RNF2 | GRCh38.p7 | 1:185076676 | TATTTGAAAAGGGTT[A/T]AAATTTTTTTTTTGT | 6045 |
rs12043617 | snp | A/G | 0.244205 | 0.249933 | intron-variant | RNF2 | GRCh38.p7 | 1:185087813 | ACAAATAATCTGAAT[A/G]CTCTATACAAGCTTT | 6045 |
rs12044161 | snp | C/T | 0.124144 | 0.21601 | intron-variant | RNF2 | GRCh38.p7 | 1:185097326 | ATCGCCTTAGCTGAC[C/T]TGGCGGAAGGTCAGC | 6045 |
rs12044346 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066236 | CCTTTGTATTGCATA[C/T]TAGGCCTCACTGATC | 6045 |
rs12044997 | snp | A/T | 0.245631 | 0.249962 | intron-variant | RNF2 | GRCh38.p7 | 1:185097520 | GTCAATTAATTCTTA[A/T]AGTCTTTTGTTTAAT | 6045 |
rs12046202 | snp | C/T | 0.255503 | 0.249939 | intron-variant | RNF2 | GRCh38.p7 | 1:185099120 | ACAGTGGCACAATCT[C/T]GGCTGACTGCAACCT | 6045 |
rs12049293 | snp | C/T | 0.245061 | 0.249951 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070798 | TGCCCGCCACCTCGC[C/T]GGCTCATTTTTTTAT | 6045 |
rs12059402 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | RNF2 | GRCh38.p7 | 1:185048040 | CCAGATATCCTGACT[G/T]TTTGCCTACTGGTCT | 6045 |
rs12062374 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | RNF2 | GRCh38.p7 | 1:185050099 | atctggACGAATAGT[A/G]TAGGTTAAGATGTAG | 6045 |
rs12070618 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185060620 | GGACTGAGAGCCTGG[A/G]TTATGCCAAAGTCTG | 6045 |
rs12077730 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185083041 | ATGGTTCACCTCAAA[G/T]TCAACAACTAGAGTC | 6045 |
rs12080414 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF2 | GRCh38.p7 | 1:185066228 | TCTTGATACCTTTGT[A/G]TTGCATACTAGGCCT | 6045 |
rs12081098 | snp | C/G | 0.498503 | 0.0273153 | intron-variant | RNF2 | GRCh38.p7 | 1:185089147 | atgcagtctagatcc[C/G]ttgcatgtgcagttc | 6045 |
rs12091158 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082367 | ttttttttttttttt[G/T]gaagacagagtcttg | 6045 |
rs12092074 | snp | G/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101832 | ATCTGTTTTTACAGG[G/T]ttttttttttttttt | 6045 |
rs12126822 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNF2 | GRCh38.p7 | 1:185066848 | AGGGGTAGTAGTAGT[C/G]TTAGAGGAGATGAGA | 6045 |
rs12127009 | snp | A/G | 0.161267 | 0.233723 | intron-variant | RNF2 | GRCh38.p7 | 1:185061415 | TTCTGATCTCAGGCA[A/G]AAACCAACCCACCAA | 6045 |
rs12145600 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076247 | GGCTGCCCTTCTTTT[C/T]TTCTAGATCTTTTAT | 6045 |
rs12408074 | snp | A/G | 0.398354 | 0.201224 | intron-variant | RNF2 | GRCh38.p7 | 1:185091886 | AATGGCACGATCTTG[A/G]CTCACTGCAACCTCT | 6045 |
rs12408279 | snp | A/G | 0.244776 | 0.249945 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070091 | TCTCCCTGGTCTTTT[A/G]CATGTTAGGGGACTA | 6045 |
rs12409926 | snp | C/T | 0.245631 | 0.249962 | intron-variant | RNF2 | GRCh38.p7 | 1:185083295 | TATTTTGTCAGTTTT[C/T]TCAGGTTCTTTGAAT | 6045 |
rs12563135 | snp | C/T | 0.418169 | 0.184985 | intron-variant | RNF2 | GRCh38.p7 | 1:185092013 | TATTTTTAGTAGAGA[C/T]GGGGTTTCAACTTGT | 6045 |
rs12749846 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056602 | tctcaaactcctggc[C/T]tcaagtgatcctccc | 6045 |
rs16865296 | snp | A/T | 0.245061 | 0.249951 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100711 | TGTATTCTGACTTTT[A/T]TTTTCCCCCGGAGTC | 6045 |
rs17314171 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | RNF2 | GRCh38.p7 | 1:185073437 | CTGTTATTCTTTTAT[C/T]CAGCCAAAGAGCAGA | 6045 |
rs17379801 | snp | C/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071326 | TTCCGGGCTAGTTTA[C/T]AGGGAAGATATGTAT | 6045 |
rs28609768 | snp | A/C | 0.435837 | 0.167226 | intron-variant | RNF2 | GRCh38.p7 | 1:185064348 | AGAATCCTACAGAAT[A/C]GGTACTTTATTTCAA | 6045 |
rs28690032 | snp | A/C | 0.498133 | 0.030494 | intron-variant | RNF2 | GRCh38.p7 | 1:185062820 | AGACCTCCCCCCCCC[A/C]AAAAAAAGGCCAATA | 6045 |
rs34086865 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078684 | GAGGCCGAGGTGGGC[-/A]GGATCACCTGAGGTT | 6045 |
rs34143770 | in-del | -/T | 0.418169 | 0.184985 | intron-variant | RNF2 | GRCh38.p7 | 1:185051735 | CTCCTTAACTAATTC[-/T]TTTTTTTTTTTCATC | 6045 |
rs34216534 | in-del | -/T | 0.154661 | 0.231107 | intron-variant | RNF2 | GRCh38.p7 | 1:185068009 | CCACAGCGCCCGGCC[-/T]TTTTTTTTTTTAGAG | 6045 |
rs34284435 | in-del | -/T | 0.499396 | 0.0173617 | intron-variant | RNF2 | GRCh38.p7 | 1:185061129 | CTATTTCTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 6045 |
rs34348424 | snp | A/C | 0 | 0 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101591 | CCAACTTTATATATC[A/C]CAGTATTTAAAAAGA | 6045 |
rs34494448 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058046 | GGAACATCACCGGAG[-/T]CCTGGGAGGGTTGAG | 6045 |
rs34522033 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051907 | AAAAAGTCGTATTTG[-/T]ATTTATACATATATT | 6045 |
rs34763973 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079900 | CGCCACTGCACTCTA[-/G]GCCTGGGCAACAAGA | 6045 |
rs34784535 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | RNF2 | GRCh38.p7 | 1:185062651 | TATAAAAGATAAAAG[-/T]TATGTACTGAAGAAG | 6045 |
rs34810150 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057344 | TAAATATAATTAACA[-/T]TTTTCTGTGCCATAG | 6045 |
rs34969721 | snp | A/G | 0.379158 | 0.214052 | intron-variant | RNF2 | GRCh38.p7 | 1:185096042 | AGTTACATTAATATA[A/G]CTCTGTCACATCAAT | 6045 |
rs34982714 | in-del | -/C | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102603 | TTCTCTTCTTCTTAA[-/C]CCCCTAGCAACCTCT | 6045 |
rs35117337 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047854 | GTTATTGCACACACT[-/G]GTAGAAGACATTGTC | 6045 |
rs35163206 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087912 | TGAAAAAGTACATAT[-/G]CTATAAAATTCACAT | 6045 |
rs35163800 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075566 | AAGGTTCTGCAAGGC[-/T]TGTACAGGAAGCATG | 6045 |
rs35165842 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087242 | ACAGTTCTGGAGACT[-/G]GGGAATTCCAAGATC | 6045 |
rs35280730 | in-del | -/A | 0.499863 | 0.00828277 | intron-variant | RNF2 | GRCh38.p7 | 1:185059228 | ATCCCAGTCTGGATT[-/A]AAAAAAAAAAAACCT | 6045 |
rs35586940 | in-del | -/A | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185088556 | TCAAAAAAAAAAAAA[-/A]GCTAAAGGAAGTATT | 6045 |
rs36053005 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | RNF2 | GRCh38.p7 | 1:185075871 | CTAAATATTAGTCAT[C/T]TTAATCTTTGTCAAT | 6045 |
rs36086867 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048834 | TAAGTTCAGCTAAGC[-/T]TTTGGTGTTGGAACA | 6045 |
rs41529047 | snp | C/T | 0.0345262 | 0.126772 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071657 | AAAGAACTGGGTGAC[C/T]ATGTTCAACTTGTCC | 6045 |
rs55738529 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | RNF2 | GRCh38.p7 | 1:185082807 | TTGTTTTTTGTCTAA[C/T]AACATTTCCATAGTC | 6045 |
rs55743893 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF2 | GRCh38.p7 | 1:185077452 | TGTTTTGGGACTTCC[A/G]GTAGATTTTTCATGA | 6045 |
rs55756628 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | RNF2 | GRCh38.p7 | 1:185074690 | ATTAGGGAAAAAAAA[C/T]GGTATGGTTGCATCT | 6045 |
rs56048451 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100881 | AGTTCTTTATGAACT[C/T]AGTGTCCATTGTCAT | 6045 |
rs56098414 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068721 | GTTATAAGCCTTCAA[-/A]TTTGTGATAATGTTA | 6045 |
rs56110440 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | RNF2 | GRCh38.p7 | 1:185067744 | GAGACGGAGTCTTGC[C/T]CTGTTGCCCAGGCTG | 6045 |
rs56121579 | snp | A/G | | | missense | RNF2 | GRCh38.p7 | 1:185098130 | GCAGAAGATAATGGT[A/G]ACAGTTCACACTGCA | 6045 |
rs56204629 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185066733 | AGGCTGCTGCTGTTA[C/T]AATTAGTGTTGACTC | 6045 |
rs56325070 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | RNF2 | GRCh38.p7 | 1:185085764 | GTTCAAGCGATTCTC[A/C]TACCTCATCCTCCCG | 6045 |
rs56691510 | snp | A/G | 0.084728 | 0.187577 | intron-variant | RNF2 | GRCh38.p7 | 1:185092326 | GGATTACAGGCGTGT[A/G]TCACCACGCCTGGCT | 6045 |
rs57050104 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | RNF2 | GRCh38.p7 | 1:185057548 | CCCCGTAAGTTTACC[C/T]TTCCAAGAATGAATC | 6045 |
rs57453569 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065963 | CTGTCTCATTTTTTT[-/T]TTTTTTAGTATCAGC | 6045 |
rs57745553 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070638 | GCAGTATTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs57914017 | in-del | -/A/AA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059240 | ATTAAAAAAAAAAAA[-/A/AA]CCTCCGTAATAGTTT | 6045 |
rs58085875 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079094 | TTTTTTTTTTTTTTT[-/TT]CGGATTTATTTTGTT | 6045 |
rs58086194 | in-del | -/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185073075 | TTTTTTTTTTTTTTT[-/T]ACTTAATGTGTGTTG | 6045 |
rs58345263 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | RNF2 | GRCh38.p7 | 1:185059933 | GGTCTCTACCTGACC[A/G]CAGATTTAATTTGCC | 6045 |
rs58830489 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185064449 | GTGGTTCGACTTACG[A/G]TTTTTCAACTTTACA | 6045 |
rs58838852 | in-del | -/TTT | 0 | 0 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101854 | TTTTTTTTTTTTTTT[-/TTT]GTAATCTGTGCCATG | 6045 |
rs59351560 | in-del | -/GTTTTTTTTTTTTTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077637 | TTGTTTTTTTTTTTT[-/GTTTTTTTTTTTTTTT]TGGCTAGAAATTTAG | 6045 |
rs59705922 | in-del | -/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076607 | TATGGTTTTTTTTTT[-/T]ATGTTAATCCTTCCA | 6045 |
rs59747322 | in-del | -/AA | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185084813 | TTCACTTTGATTCAC[-/AA]GAGAGAGTTGCCATA | 6045 |
rs59997641 | in-del | -/AT/ATAT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051969 | TATATATATATATAT[-/AT/ATAT]GCATGCACCCATGTA | 6045 |
rs60213064 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082367 | TTTTTTTTTTTTTTT[-/TT]GAAGACAGAGTCTTG | 6045 |
rs60334821 | in-del | -/CTCT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077324 | CTTCTCTCCCTCCCT[-/CTCT]ATTTTTTTTCCTACC | 6045 |
rs60678736 | in-del | -/T | 0.175901 | 0.238766 | intron-variant | RNF2 | GRCh38.p7 | 1:185100182 | TTTCATAATTTTTTC[-/T]TTTCTTTTTTGTTTT | 6045 |
rs60738706 | snp | A/G | 0.0287284 | 0.116357 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101697 | CTGTCTAGTCATTGT[A/G]AATATTTATCTGTCA | 6045 |
rs61146985 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | RNF2 | GRCh38.p7 | 1:185081829 | TTTTCGGTGCATCTC[A/G]ATTTGCTGAGCATAT | 6045 |
rs61826108 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185050143 | GAATTCTGTGTTAAC[A/G]TTGCCTTTCAAAAAG | 6045 |
rs61826109 | snp | A/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185053888 | ACTTAATGTCTTGTA[A/T]TAAAAAAAAAAGTCA | 6045 |
rs61826143 | snp | G/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076595 | CCGGCCTTATTTTAT[G/T]GTTTTTTTTTTTATG | 6045 |
rs66657295 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095816 | TTTACAAATATTTTT[-/A]TGTAGGTATATGTTC | 6045 |
rs67590844 | in-del | -/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100550 | TTCTTGTGTTTTTTT[-/T]TTTTCCCCACAAAGT | 6045 |
rs67661434 | in-del | -/TTAG | 0.24449 | 0.249939 | intron-variant | RNF2 | GRCh38.p7 | 1:185055856 | TTGATCTTAAAATTT[-/TTAG]TTAGCATATTTGTGA | 6045 |
rs71101959 | in-del | -/AC | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076268 | AAAAAAAAAAAAAAA[-/AC]CACCCCATAAAAGAT | 6045 |
rs71297840 | multinucleotide-polymorphism | ACAA/CCAC | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076266 | AAAAAAAAAAAAAAA[ACAA/CCAC]CCCATAAAAGATCTA | 6045 |
rs71555455 | in-del | -/TT | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185085166 | TTTTTTTTTTTTTTT[-/TT]GAGACAAAGTCTCAC | 6045 |
rs71634124 | snp | C/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076234 | TATCTTGCTTTTAGG[C/G]TGCCCTTCTTTTCTT | 6045 |
rs71634125 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076242 | TTTTAGGCTGCCCTT[C/T]TTTTCTTCTAGATCT | 6045 |
rs71634126 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076250 | TGCCCTTCTTTTCTT[C/T]TAGATCTTTTATGGG | 6045 |
rs71634127 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185076256 | TCTTTTCTTCTAGAT[C/T]TTTTATGGGGTGGTT | 6045 |
rs71634128 | snp | A/C | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185089892 | AAAAATTAGCCAGGC[A/C]TGGTGGTGCACACCT | 6045 |
rs71634129 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185089904 | GGCCTGGTGGTGCAC[A/G]CCTGTAATCCCAGCT | 6045 |
rs72392086 | in-del | -/TAA | 0.2776 | 0.248472 | intron-variant | RNF2 | GRCh38.p7 | 1:185064685 | TCTTTATTGTTATCT[-/TAA]TAATATTTTGTCTTC | 6045 |
rs72637296 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF2 | GRCh38.p7 | 1:185067600 | ATTAAAAGAGAGAGA[A/G]GGCATCTTAGTTTTT | 6045 |
rs72739692 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185059537 | ACTTCCAGTCATTAC[A/G]TATGGTATTAATTGT | 6045 |
rs72739693 | snp | C/T | 0.310386 | 0.242597 | intron-variant | RNF2 | GRCh38.p7 | 1:185061102 | CTCCACTCTGGGTGC[C/T]GGAGTGAGACCCTAT | 6045 |
rs72739697 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | RNF2 | GRCh38.p7 | 1:185072240 | TATCTGGACTCTCAT[G/T]TTGAGGGGTTTTTGG | 6045 |
rs72739698 | snp | C/T | 0.312593 | 0.242037 | intron-variant | RNF2 | GRCh38.p7 | 1:185073579 | AGTTTTTTAAAAGGA[C/T]ACATAAATGTGATTG | 6045 |
rs72739699 | snp | A/G | 0.277867 | 0.248442 | intron-variant | RNF2 | GRCh38.p7 | 1:185073823 | GTTTTTTGCTACACT[A/G]ACAATTCTCCAACTC | 6045 |
rs72741805 | snp | A/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102314 | CACTACCAACCAGGG[A/T]TTCAAAAAGTATTAC | 6045 |
rs73066911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185082944 | ATTCCAGTATCAAAT[A/G]GTGAATTCCAACAGT | 6045 |
rs74134409 | snp | A/C | 0.0244538 | 0.107838 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045176 | AACCCCAGAAGCCGG[A/C]CAGGAAGGTGTAAAG | 6045 |
rs74134410 | snp | A/G | 0.120674 | 0.21395 | intron-variant | RNF2 | GRCh38.p7 | 1:185057806 | ATTACTCTAAAGGGG[A/G]AAAAAAAAAAAAACA | 6045 |
rs74134412 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RNF2 | GRCh38.p7 | 1:185071920 | CTCATTATATTTTCT[C/T]TCCTCATGACATTGG | 6045 |
rs74134413 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF2 | GRCh38.p7 | 1:185095462 | ATCTGCTTAAGTTCT[C/T]ATCTTCCATTCTAGG | 6045 |
rs74358744 | snp | C/G | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185081600 | GTGGGGTGGGGGGGG[C/G]CGGTTTCACCATGTT | 6045 |
rs74471398 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090806 | GAGAGGGTAGTGAAC[A/C]AAGTAGGATTCACTA | 6045 |
rs74627154 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185082114 | ACTTAAAAATGGCGA[C/T]ATTTTTGATTTTCAC | 6045 |
rs74656923 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074891 | ATAAGGGACTTGAGT[A/C]TCCATGGATTTTGGT | 6045 |
rs74675570 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185059845 | TGGGTTATTCCAGTT[C/T]CTGTTAGAAGAGTGT | 6045 |
rs74684837 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | RNF2 | GRCh38.p7 | 1:185054081 | ATATGTGTACTTATT[C/G]TTTATAACTAGTGTC | 6045 |
rs74697315 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185058602 | TATTGTTCGGTAATG[G/T]GGAATGAGTTTTGCT | 6045 |
rs74698247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074459 | TCTAGGGGCCCACCT[A/G]GAGTAACCATATTAG | 6045 |
rs74713114 | snp | G/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185061142 | TCTTTTTTTTTTTTT[G/T]TTTGAGACGGAATCT | 6045 |
rs74809352 | snp | C/T | 0.0327778 | 0.123752 | intron-variant | RNF2 | GRCh38.p7 | 1:185064491 | GCAATATGCATTCAG[C/T]ATGCTCCTTGACTTG | 6045 |
rs74880221 | snp | A/G | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185049682 | GTGTAAAAAAAAAAA[A/G]GCGGGGGAGGGGGGA | 6045 |
rs75166128 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185094059 | TTACTCCCTACTTCT[C/G]TTCATTCTTACTCAT | 6045 |
rs75300063 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077934 | TAAGGTAGTATTTTC[A/G]TTTTATTCATTTATA | 6045 |
rs75429623 | snp | C/T | 0.030665 | 0.119967 | intron-variant | RNF2 | GRCh38.p7 | 1:185097688 | ATAGGTGCACCACCA[C/T]GCCCAGCTAATTAAA | 6045 |
rs75450270 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | RNF2 | GRCh38.p7 | 1:185071895 | GTTGGTTGTGCAGCT[C/G]TGTCACTTTCTCATT | 6045 |
rs75495382 | in-del | -/TTG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061144 | TTTTTTTTTTTTTTT[-/TTG]AGACGGAATCTCGCT | 6045 |
rs75663590 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185046306 | AAACCGTGAGCTTAC[A/C]CAGGAGGAGTCGTGG | 6045 |
rs75684319 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | RNF2 | GRCh38.p7 | 1:185066124 | CTCATCTCTTCAGAT[C/T]ATTGCACAGATTAGG | 6045 |
rs75712051 | snp | G/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185067729 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 6045 |
rs75812438 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074895 | GGGACTTGAGTATCC[A/G]TGGATTTTGGTATCG | 6045 |
rs75880720 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185054993 | GCATGAGCCAATGCA[C/T]CTGCTGTTTCTTTTC | 6045 |
rs75895512 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RNF2 | GRCh38.p7 | 1:185048439 | ATTTCTATTGCTTAA[A/G]TTTACTTCTCCCATT | 6045 |
rs75898672 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | RNF2 | GRCh38.p7 | 1:185080000 | AGGCCCCCAGTAGAC[C/T]TAGATCTTGTTCAGT | 6045 |
rs75953491 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185053783 | AAATATCTAAAAGGA[A/G]TAGTGCACGTGACAT | 6045 |
rs75966617 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | RNF2 | GRCh38.p7 | 1:185058067 | GAGGGTTGAGGCTGC[A/C]GTGAGCCTTGATTGC | 6045 |
rs76046313 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | RNF2 | GRCh38.p7 | 1:185058648 | TTTGCTACTTTAACT[A/G]CTTAAGTTTTTCTTT | 6045 |
rs76048610 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074894 | AGGGACTTGAGTATC[C/T]ATGGATTTTGGTATC | 6045 |
rs76097792 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185079930 | AGCGAGACTGTCTCA[A/G]AAAAAAAAAAAAGCC | 6045 |
rs76112967 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185085013 | CACTCTACCTTAGTG[G/T]TCCCTGAGTAGCTGG | 6045 |
rs76268150 | snp | G/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185056377 | TTCTCATTTTTTTTA[G/T]AGACAGGGCCTCCCT | 6045 |
rs76272189 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | RNF2 | GRCh38.p7 | 1:185065876 | GTTTCCTTTTTTTCC[C/T]CCCTACTTGCTCTAG | 6045 |
rs76287709 | snp | C/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185096604 | TTATTTATTTCTCTT[C/T]TTACTTGACTGTAGG | 6045 |
rs76301737 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071644 | CCCCGCCAATCTTGG[A/G]CAAGTTGAACATGGT | 6045 |
rs76488232 | snp | A/G/T | 0.0654984 | 0.168698 | intron-variant | RNF2 | GRCh38.p7 | 1:185080211 | CTACTCTGTGTATAT[A/G/T]TTAGTATCTATACAT | 6045 |
rs76496453 | in-del | -/CT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073059 | TTGCTCTACGACTTG[-/CT]TTTTTTTTTTTTTTT | 6045 |
rs76599420 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185049683 | TGTAAAAAAAAAAAA[A/G]CGGGGGAGGGGGGAA | 6045 |
rs76690809 | snp | C/T | 0.039522 | 0.134904 | intron-variant | RNF2 | GRCh38.p7 | 1:185065479 | GTCGGCACTACTACC[C/T]TTATGAGCTGTAACA | 6045 |
rs76748674 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185072149 | GAGGAGGTAGCAGGG[A/G]GCTGACTCTGAGGTG | 6045 |
rs76775396 | snp | A/C | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185057820 | GAAAAAAAAAAAAAA[A/C]AGTAAAACAGTTCAA | 6045 |
rs76797771 | snp | A/T | 0.0379877 | 0.132479 | intron-variant | RNF2 | GRCh38.p7 | 1:185062438 | TCATGAATTAGAAGA[A/T]AGCATGCTAACTTAT | 6045 |
rs76829139 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185079532 | TTCTGTTTCTGCTTT[C/T]TTCAGCCTTTTTCTG | 6045 |
rs76902199 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF2 | GRCh38.p7 | 1:185096914 | TTCTTTGTTCTGGCA[A/G]TAAACATAATGACAA | 6045 |
rs76943390 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185097824 | ACAGGTGTGAACCAC[C/T]GTGCCTGGCCAGTAA | 6045 |
rs76955037 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087751 | TAAATTTATATTCAA[A/G]CATTCCTGACTTCTG | 6045 |
rs76973251 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185056364 | CTTTTTTTTTTTTTT[C/T]TCATTTTTTTTAGAG | 6045 |
rs77087412 | snp | A/G | 0.021333 | 0.101051 | intron-variant | RNF2 | GRCh38.p7 | 1:185064927 | TGTTTTTTTCTTGCA[A/G]CGTTGCTGAATTCAT | 6045 |
rs77127258 | snp | C/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185062453 | TAGCATGCTAACTTA[C/T]CAGTGGAGAAGAGAG | 6045 |
rs77216883 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185064766 | CTTTCAGAATGTTTT[G/T]TAATTTTCATTATGC | 6045 |
rs77256109 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084277 | CCATGCCTTAATTCA[G/T]TTTATGTTGGCTTAC | 6045 |
rs77310047 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185063649 | CTATTTTACAGTTCT[A/G]GCAGTAAGAAGTCCA | 6045 |
rs77336081 | snp | G/T | 0.0759472 | 0.179459 | intron-variant | RNF2 | GRCh38.p7 | 1:185059944 | GACCACAGATTTAAT[G/T]TGCCAACAGACTGTG | 6045 |
rs77338610 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF2 | GRCh38.p7 | 1:185054394 | CCGGAGAGGACGTGT[C/T]AAGGCTGGACACTGT | 6045 |
rs77339682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076987 | CAGATCCTCTTTAAT[A/G]TACTTCAGTTAAGTT | 6045 |
rs77430484 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RNF2 | GRCh38.p7 | 1:185059670 | GGCTAAGAGCATGGC[C/G]TTCTCACTCAGACCT | 6045 |
rs77460284 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185076597 | GGCCTTATTTTATGG[G/T]TTTTTTTTTTATGTT | 6045 |
rs77515893 | snp | A/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185053351 | TTTTCTTTTTTTTTT[A/T]AAGAGACAGGATCTT | 6045 |
rs77552067 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | RNF2 | GRCh38.p7 | 1:185077727 | TTTGTTTTTTTTTTT[G/T]GGGCTGTTGTTGTTT | 6045 |
rs77879280 | snp | A/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185053890 | TTAATGTCTTGTATT[A/T]AAAAAAAAAGTCACT | 6045 |
rs77989270 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185056376 | TTTCTCATTTTTTTT[A/G]GAGACAGGGCCTCCC | 6045 |
rs78070437 | snp | G/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185077638 | TTGTTTTTTTTTTTT[G/T]GGCTAGAAATTTAGC | 6045 |
rs78198284 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070643 | ATTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTGA | 6045 |
rs78228441 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185073091 | ACTTAATGTGTGTTG[G/T]ATACATATATTGAGT | 6045 |
rs78275311 | snp | C/G | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185095517 | GCCTCATTTTTTTCC[C/G]ATAGCACGTATCACT | 6045 |
rs78276836 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | RNF2 | GRCh38.p7 | 1:185058663 | ACTTAAGTTTTTCTT[C/T]ATTGTGTTATGGTTT | 6045 |
rs78418182 | snp | G/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185053354 | TCTTTTTTTTTTTAA[G/T]AGACAGGATCTTGCT | 6045 |
rs78489984 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185073062 | CTCTACGACTTGCTT[C/T]TTTTTTTTTTTTTAC | 6045 |
rs78512357 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | RNF2 | GRCh38.p7 | 1:185090652 | GGAAACAGGAAGCAC[A/G]GGAGCGTATTGAAAG | 6045 |
rs78568529 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185057015 | CTAAATTTATGTGTG[C/T]TTTAAAACCTGGGCT | 6045 |
rs78773191 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185059721 | ACATTTACTATGAGA[A/C]CATTAAGCACGTTAA | 6045 |
rs78871440 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RNF2 | GRCh38.p7 | 1:185063771 | AACTTCTGGAGGTTA[C/T]CTGCATTCTAATTTG | 6045 |
rs78968119 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077640 | GTTTTTTTTTTTTTG[C/G/T]CTAGAAATTTAGCTA | 6045 |
rs78973166 | snp | A/C | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185088759 | GAAAAATTTTCACAA[A/C]GTTCCAAAAACCAAA | 6045 |
rs79024553 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185085798 | AGCTGGGATTACAGA[C/T]GCGCACCACCACACC | 6045 |
rs79091515 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185057776 | TCCTTGGATTCAACA[A/G]ACTGCAGGTGGAAAA | 6045 |
rs79131595 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF2 | GRCh38.p7 | 1:185069118 | TCTTTTGCCTGTTAA[C/T]GTGCTATTTATTATG | 6045 |
rs79139070 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RNF2 | GRCh38.p7 | 1:185097075 | TTCTGGCACTTATTA[A/G]CTGTATAACTGGAGG | 6045 |
rs79308877 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094144 | CAGTTTTTTTTTTTT[A/T]TTTTTTTTATTTTTT | 6045 |
rs79402558 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076480 | TATTTTTAGTAGAGA[C/T]GGGATTTTACCGTGT | 6045 |
rs79412434 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | RNF2 | GRCh38.p7 | 1:185050649 | AGACATCATTTCTTC[C/G]TTCCAAGGTCATTAG | 6045 |
rs79451745 | snp | C/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185056362 | TTCTTTTTTTTTTTT[C/T]TCTCATTTTTTTTAG | 6045 |
rs79526782 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185064324 | TAATAGCTATTGTTT[A/G]TTCTTCATAGAATCC | 6045 |
rs79528293 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185084144 | AGATGGCTTCTTGCT[A/G]TGTTGCCCAGAATGG | 6045 |
rs79595520 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF2 | GRCh38.p7 | 1:185087914 | GAAAAAGTACATATC[C/T]ATAAAATTCACATGT | 6045 |
rs79597165 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RNF2 | GRCh38.p7 | 1:185066403 | GTCCTTCAGGACTGC[C/T]TTCTTTCCTCGCTTG | 6045 |
rs79710475 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185058042 | AGGTGGGAACATCAC[C/T]GGAGCCTGGGAGGGT | 6045 |
rs79732780 | snp | A/C | 0.00623005 | 0.0554636 | missense | RNF2 | GRCh38.p7 | 1:185099942 | ACCATTTATATAGCA[A/C]CAGCCAGTGGCCAGT | 6045 |
rs79740909 | snp | C/T | 0.0228947 | 0.104514 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101866 | TTTTGTAATCTGTGC[C/T]ATGAAATTTGAAAAC | 6045 |
rs79877600 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185053341 | CTTTTTTTCTTTTTC[C/T]TTTTTTTTTTAAGAG | 6045 |
rs79998715 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | RNF2 | GRCh38.p7 | 1:185064457 | ACTTACGATTTTTCA[A/G]CTTTACAGTGGTACA | 6045 |
rs80062866 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | RNF2 | GRCh38.p7 | 1:185080901 | CAGTAGGCAGAAGGA[A/G]TGTTCTGCTTATAAT | 6045 |
rs80158366 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185096031 | ACGCTGCCTGCAGTT[A/T]CATTAATATAGCTCT | 6045 |
rs80168233 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185066203 | TCTTCGTCATTGCAC[C/T]GTGGATCTTTCTTGA | 6045 |
rs80255902 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | RNF2 | GRCh38.p7 | 1:185093435 | CCAGGCATAATAGGG[C/T]ATTTCATTTAAAATA | 6045 |
rs80323231 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | RNF2 | GRCh38.p7 | 1:185058189 | TACATAGCATTTATA[G/T]TGTATTAGGTAGTAT | 6045 |
rs111301848 | in-del | -/A | 0.366885 | 0.220993 | intron-variant | RNF2 | GRCh38.p7 | 1:185057806 | ATTACTCTAAAGGGG[-/A]AAAAAAAAAAAAACA | 6045 |
rs111336236 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185085258 | GGTTCATGCTATTCT[A/C]CTGCCTCAGCCTCCC | 6045 |
rs111411120 | snp | A/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185089810 | CGAGGCCGGTGGATC[A/T]CCTGAGGTCAGGAGT | 6045 |
rs111570137 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185081310 | CCTGCAAAAAGTTGT[C/T]AAGATGCTTGAAGAA | 6045 |
rs111644230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094899 | GTCTAGTGGTTTTCA[C/T]CTTGGCTGAACATCA | 6045 |
rs111664205 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185099252 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTC | 6045 |
rs111732413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049244 | GATCTCATGCCACAC[C/T]ATCAGAGGATGTGAG | 6045 |
rs111732754 | snp | C/T | 0.5 | 0 | missense | RNF2 | GRCh38.p7 | 1:185099928 | GTGAGAAGCAGTATA[C/T]CATTTATATAGCAAC | 6045 |
rs111816430 | snp | A/G | 0.5 | 0 | missense | RNF2 | GRCh38.p7 | 1:185100265 | AGTGAACAAACCCAT[A/G]GAACTTTATTACGCA | 6045 |
rs111821047 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185052508 | TTCTGTGAAATATCC[A/G]GAATAGAAAAATCCA | 6045 |
rs111908854 | in-del | -/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185098758 | AATCCTCAAATTAAC[-/T]TTTTTTTTTTTTGAG | 6045 |
rs112028214 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | RNF2 | GRCh38.p7 | 1:185067251 | CTTTAGAAGCTTACA[A/G]AAATTAGCGTCTGTC | 6045 |
rs112142583 | snp | G/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185055543 | CTCCTGCCTCCTGAG[G/T]AGCTGGGATTACAGG | 6045 |
rs112215933 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185062452 | ATAGCATGCTAACTT[A/G]TCAGTGGAGAAGAGA | 6045 |
rs112273030 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185051277 | GTTTTCTAGAAGGCT[C/T]TACTGTATTACAGAA | 6045 |
rs112287412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091975 | CATTGCCACCGTGGC[C/T]GGCTAGTTTTTTTTT | 6045 |
rs112305839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095277 | CTAGTGGTGGGGCTG[C/T]ATGATAGGCACTCCT | 6045 |
rs112446106 | in-del | -/G | 0.0391387 | 0.134304 | intron-variant | RNF2 | GRCh38.p7 | 1:185075742 | ACACGAGAACAGCAA[-/G]GGGGAAATCCACTCC | 6045 |
rs112474141 | snp | A/C/T | 1.66203e-05 | 0.00288268 | intron-variant | RNF2 | GRCh38.p7 | 1:185099980 | GAGTATTTAAAATAA[A/C/T]AGACTGTTGAAACTG | 6045 |
rs112784848 | snp | G/T | 0.0387552 | 0.1337 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070872 | CGATTTCCTGACCTC[G/T]TGATCCGCCCGCCTC | 6045 |
rs112862343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057000 | ATTTTATATGTAGAT[C/T]TAAATTTATGTGTGT | 6045 |
rs112864631 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059148 | CCAGAAGAGAAGAGA[C/G]AGATTAAGTTAGTCT | 6045 |
rs112890078 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044950 | GACCACAATCAGAAT[A/G]TTAAGCTAAGTTTAG | 6045 |
rs113084414 | in-del | -/TCT | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185084217 | CACCCAGTCTTTAAG[-/TCT]TCTTCTAGCTATCTG | 6045 |
rs113094735 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | RNF2 | GRCh38.p7 | 1:185081423 | TTTGAGGTGGAGTTT[C/T]GCTCTTGTTGCCCAG | 6045 |
rs113190581 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185086771 | AAAGAGGCAGAATGA[C/T]TAGTGGTTTAAAGTG | 6045 |
rs113287876 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061191 | GGAGTGCAGTGGCGG[G/T]ATCTCGGCTCACTGC | 6045 |
rs113454769 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070887 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 6045 |
rs113861270 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RNF2 | GRCh38.p7 | 1:185090275 | CTTTTTCTTTTCCCC[C/T]ACAGTGCTACACATC | 6045 |
rs113867351 | snp | C/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185092786 | TTAAATTAGAAAAAA[C/T]AGATTTTTATTTCTA | 6045 |
rs113970151 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185054214 | ACGCAACGGGTTTCA[A/G]TATGCCTTGGACTAA | 6045 |
rs113970520 | snp | A/G | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185100086 | TGTTAAGTGACAAGT[A/G]GTTATTCCTAAGATT | 6045 |
rs114020823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185095599 | ACTATGTCAGTATCA[C/T]TGATTCTTATTAACA | 6045 |
rs114049596 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185046408 | CTAGTACCCACTTTT[A/G]CCGGGAGCCCACGTC | 6045 |
rs114192030 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | RNF2 | GRCh38.p7 | 1:185073923 | ACCCCACACATTAAG[A/G]GATCAGTCCCACAAG | 6045 |
rs114206837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074222 | CCTTCTGGCACCCTG[A/G]CCTTCCACGAGTTCC | 6045 |
rs114210266 | snp | C/T | 0.00397018 | 0.0443771 | intron-variant | RNF2 | GRCh38.p7 | 1:185099987 | TAAAATAATAGACTG[C/T]TGAAACTGGGAGCAC | 6045 |
rs114357643 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | RNF2 | GRCh38.p7 | 1:185079511 | AAACAACCAGTCTGC[G/T]TTTTGTTCTGTTTCT | 6045 |
rs114409835 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185055976 | CAAATAATTGTAAAG[C/T]AATGTATGTTTTTAA | 6045 |
rs114442839 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185077152 | TTTTGGCATTTTTTT[A/T]ATCTTCATTCCACCA | 6045 |
rs114477763 | snp | A/C/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185088703 | TACATGGGGTTCTGC[A/C/G]TCTGTGGATTCAAGC | 6045 |
rs114496275 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | RNF2 | GRCh38.p7 | 1:185057323 | AAATAAATAAATAAA[C/T]AAAATCTAAATATAA | 6045 |
rs114534341 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102593 | AAGTAATGCATTTCT[A/C]TTCTTCTTAACCCCT | 6045 |
rs114731227 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | RNF2 | GRCh38.p7 | 1:185065978 | TTTTTTTAGTATCAG[C/T]ATCTACACAGCCACA | 6045 |
rs114829772 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185077503 | ATTTCTAACTTATTA[C/T]GACTTTTATTAGAAA | 6045 |
rs114934913 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100691 | ATACAGAATGTTAAA[C/T]ATTATGTATTCTGAC | 6045 |
rs114950935 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185058082 | AGTGAGCCTTGATTG[C/T]GCCTTTGCATTCCAG | 6045 |
rs114995260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088087 | TGAGATTCCTATACA[A/G]CAGGCAGGCAGAGAT | 6045 |
rs115173123 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185052850 | AGGGTCAGCAAGTGT[G/T]GCTTCAAAGCTCTGC | 6045 |
rs115187030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054001 | AATCTACATTCCCCC[C/T]CCACCCAGTGTTTCT | 6045 |
rs115284030 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF2 | GRCh38.p7 | 1:185074982 | GACTATATATAGTTC[C/T]GTGTGTGTGTGTGTG | 6045 |
rs115313596 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RNF2 | GRCh38.p7 | 1:185079334 | CTTGCACTGGACCCC[A/G]CCAGACCAGAACAAA | 6045 |
rs115391600 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185068783 | TTGTTCAGAATGTAA[A/G]TGGACATTTCTAAGT | 6045 |
rs115514080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185083130 | TTGTTTGCTAATACG[A/G]AACAAAGCCTCTTAT | 6045 |
rs115593466 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | RNF2 | GRCh38.p7 | 1:185058315 | TGGCTTTTGGTGTCT[C/G]TGGTGTGCGGGGTAT | 6045 |
rs115607513 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185092618 | TTTGAGGAAATTACA[A/G]CGCATAAAACCACGA | 6045 |
rs115757443 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | RNF2 | GRCh38.p7 | 1:185062881 | ATTGAGGCTTGCCAA[G/T]TAAAACAACAAAGAA | 6045 |
rs115769201 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185072343 | ACCATTGATGAGTTC[G/T]TAAGCAAATATTTAT | 6045 |
rs115938368 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | RNF2 | GRCh38.p7 | 1:185074020 | TTGGGGATTTCCGCA[A/T]TCCCCTTGTCAGGTT | 6045 |
rs116059576 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185089693 | AGAAATGGAGCAAAA[A/G]CTGGAGACCAATGTG | 6045 |
rs116085621 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RNF2 | GRCh38.p7 | 1:185060674 | CTAGATTTAAATAAA[C/T]TGGATGAATCAGTAG | 6045 |
rs116113875 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071427 | TATGGATGAGGCTAC[A/G]TATGTCTTGGTTGTG | 6045 |
rs116183024 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185062668 | ATGTACTGAAGAAGT[C/G]AAAGACAAAAGACAA | 6045 |
rs116229287 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185085680 | TTTTTTTGAGACTAA[A/G]TGTCGCTCTGTCGCC | 6045 |
rs116295454 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101235 | CTTATTTGTAGCCAC[A/G]TAAGTTTCAAGAATA | 6045 |
rs116351476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072002 | TGAATAGGTAGATGT[A/G]GAGACAAAGCTAGAG | 6045 |
rs116430801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185049741 | CAGAGAAGAGGTTCT[A/G]TGGACCCGGTGCTGG | 6045 |
rs116459225 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185074000 | TCTGACCAATTGGCT[A/G]TAAGTTGGGGATTTC | 6045 |
rs116546744 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185085491 | GTGCTCTCTCTAATT[C/T]CGTCTCTGTGTCCAT | 6045 |
rs116576477 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185066237 | CTTTGTATTGCATAC[C/T]AGGCCTCACTGATCT | 6045 |
rs116651968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086611 | TATTTGAAAGGCTGT[A/C]ATGTAGAAAAATTAT | 6045 |
rs116693940 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RNF2 | GRCh38.p7 | 1:185096569 | TTTTGGGGTTTTTTT[G/T]TTGTTGTTGTTATTT | 6045 |
rs116854929 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185057032 | TTAAAACCTGGGCTG[C/G]GTGCGGTGGCTCATG | 6045 |
rs117020114 | snp | A/G | 0.0763149 | 0.179815 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045676 | GGGCGGGGAGGCGAA[A/G]GACGCGGAAGCAGCG | 6045 |
rs117022741 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101645 | CCTAAAGGGTTTTCA[A/G]TAGGGTGTAGACCTC | 6045 |
rs117061237 | snp | A/C | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185071978 | CATTGTGGACAAAGT[A/C]GTAAGACATGAATAG | 6045 |
rs117221824 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | RNF2 | GRCh38.p7 | 1:185065163 | ATTGTAAATTTACCA[A/G]TCAGCCCTCTGTGTC | 6045 |
rs117232442 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185052372 | TATAAACTTACAGTG[A/G]AATATTATTCAGCCA | 6045 |
rs117237809 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185081823 | TTGCAGTTTTCGGTG[C/G]ATCTCGATTTGCTGA | 6045 |
rs117477464 | snp | C/T | 0.0232847 | 0.105357 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101978 | CCACTGAATATAACC[C/T]TGGTTTTGTGATAAA | 6045 |
rs117669733 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185048449 | CTTAAATTTACTTCT[C/T]CCATTTCATTTTGAG | 6045 |
rs117932816 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185085592 | GTTAGTTGCTTTCTA[G/T]TCTTCTACCTTCTAT | 6045 |
rs118022317 | snp | C/T | 0.18 | 0.24 | intron-variant | RNF2 | GRCh38.p7 | 1:185084231 | AGTCTTCTAGCTATC[C/T]GTTGGCTTTAATTGT | 6045 |
rs118037733 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185053446 | CTCAAGTGATCCTCC[C/T]GCCTCAGCCGCCTTT | 6045 |
rs118106018 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185092370 | TTAGTAGAGGGGGGC[G/T]TTCACTGTGTTGGTC | 6045 |
rs118153445 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | RNF2 | GRCh38.p7 | 1:185089950 | TTTTTGAGACAGAGT[A/C]TCGCTCTGTCACCTA | 6045 |
rs137952785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063501 | TTGAGCAAATAAACC[A/G]AAGTTCGCATTTTTT | 6045 |
rs138004873 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046052 | TCCGGAGGCGGACGG[A/C]GTGGAATGCGAGTTT | 6045 |
rs138066439 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RNF2 | GRCh38.p7 | 1:185081703 | GTGTGAGCCACCGTG[C/T]CTGGCCTCTGTCAAC | 6045 |
rs138102798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068647 | TACTTTTATTTTGGC[C/T]CAGTGATATTGAATT | 6045 |
rs138141542 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | RNF2 | GRCh38.p7 | 1:185050338 | AAAGACAGCAACCAA[C/G]TTGCCTCTTCTCTGC | 6045 |
rs138265617 | snp | C/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185055461 | GTTCTCACTTTGCTC[C/T]TCAGGCTGGAGTGCA | 6045 |
rs138276578 | snp | C/T | 0.000197948 | 0.0099466 | intron-variant | RNF2 | GRCh38.p7 | 1:185087677 | AAGGGGCATATGAGA[C/T]GTGTAAACTGGGATA | 6045 |
rs138520184 | snp | A/T | 0.00636936 | 0.0560724 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102834 | GCAGTGAACATTATT[A/T]TAGAAGTATATAATT | 6045 |
rs138561664 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | RNF2 | GRCh38.p7 | 1:185067833 | CTCCTACCTCAGCCT[C/T]TCGAGTAGCTGGGAC | 6045 |
rs138572235 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185095662 | GTAGCTGCTCAGTAA[A/G]TATTTATCTATGTGT | 6045 |
rs138605460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071327 | TCCGGGCTAGTTTAT[A/G]GGGAAGATATGTATC | 6045 |
rs138631564 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053890 | TTAATGTCTTGTATT[-/A]AAAAAAAAAGTCACT | 6045 |
rs138661471 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF2 | GRCh38.p7 | 1:185087180 | TCCATTTAGCCTGCT[A/G]TAAAAAATACTTTAG | 6045 |
rs138766472 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185046501 | GTAAAAATTGATCTC[A/C]AACTTTGAGGTTCAT | 6045 |
rs138885156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072486 | AGAGAGAACGTGAGA[C/T]AAAGAATTACAAGGT | 6045 |
rs138891108 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | RNF2 | GRCh38.p7 | 1:185096368 | CCTCAAAGCTGAACA[C/G]TCACAATGTTGTGCA | 6045 |
rs138949005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078257 | ATCATAAATCAGTCA[A/G]TCATGTAGTTTCAAG | 6045 |
rs138959547 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185067601 | TTAAAAGAGAGAGAA[A/G]GCATCTTAGTTTTTC | 6045 |
rs139030700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185053038 | AACTGAGGAATTAAG[A/G]AGTTTAAATGAGGTC | 6045 |
rs139147020 | snp | C/T | 4.95242e-05 | 0.0049759 | missense | RNF2 | GRCh38.p7 | 1:185098317 | CTCATCCCACACTTA[C/T]GGAAAAAGATGACAG | 6045 |
rs139153032 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185057530 | TAAAGCAGTACCTGT[A/T]GTCCCCGTAAGTTTA | 6045 |
rs139306366 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185050981 | TGTCCACTCTTTGTT[A/G]TCTTTTTTTCTCCTT | 6045 |
rs139326166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074319 | AATTAGCTGGATCTC[C/T]AAACTCTTTTCCCTC | 6045 |
rs139380146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094941 | AAAACTTTCAAATCT[C/T]ATGGCTTTAGGCATC | 6045 |
rs139442978 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185097825 | CAGGTGTGAACCACC[A/G]TGCCTGGCCAGTAAA | 6045 |
rs139463884 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185094601 | GTTTTTCTACTTCCC[A/T]TGCTTACTCCCACAT | 6045 |
rs139497476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185047911 | GATTCATTTATTTGA[C/T]ATCTAAGCTGTCATA | 6045 |
rs139512469 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185084025 | TACCTCACTGAAACT[G/T]TAAACTCCTGGGCTC | 6045 |
rs139530656 | snp | G/T | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185090065 | TAGCTGGGATTACAG[G/T]CGTGTGCCACCATGC | 6045 |
rs139575368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185099705 | TTTTACTTAGTTTTT[A/G]AGAAATGTATTAGTT | 6045 |
rs139595899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093737 | TCTTCACCTGGCTTT[C/G]AGGAGGCCATAGTCT | 6045 |
rs139741360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185079397 | TAATCAAACTTGGAA[A/G]TAGGTCAGTTTTCTA | 6045 |
rs139760812 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053890 | GTATTAAAAAAAAAA[-/A]GTCACTACCTAGATG | 6045 |
rs139778083 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185080242 | AGGTGACTCTCAGAT[A/G]TTGTTCATTGAAATC | 6045 |
rs139812316 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185063972 | CAGGATAATCTCCCC[A/G]TCTTAAGAGCTGTAA | 6045 |
rs139948806 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185084643 | TAGAGCTTCTCTTAG[C/G]TGTATTATCTTTGAT | 6045 |
rs139991078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185058431 | GGTGAGAGTTCCTTA[C/T]TTTCATCAGATTCTT | 6045 |
rs140002491 | in-del | -/AT | 0.247053 | 0.249983 | intron-variant | RNF2 | GRCh38.p7 | 1:185051953 | TATATACATTTTTAC[-/AT]ATATATATATATATA | 6045 |
rs140089272 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF2 | GRCh38.p7 | 1:185089975 | CACCTAGGCTGGCAT[A/G]CAGTGGCGTGATCGC | 6045 |
rs140237001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076933 | GATTGGGATTGCATT[A/G]CATTGAATTTATATA | 6045 |
rs140345347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091319 | ATACCAGACTAATTT[C/T]CCACTAGTAAGCTTT | 6045 |
rs140367658 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044185 | GTAGAGTCAGATAAC[C/T]GTCACTTGTTATTTA | 6045 |
rs140487988 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185049718 | ACAGTAATCAGAACC[A/T]AAGAGCTCAGAGAAG | 6045 |
rs140501654 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185069165 | ATACTATTGAAAATA[C/T]ACATTTGGCTGGGTG | 6045 |
rs140670199 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071162 | AAATCTATACTTTAC[A/T]TATGAAAAGAGGGAG | 6045 |
rs140702743 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185075803 | CCTCCAACACTGGGG[A/T]TTATAATTCCACATG | 6045 |
rs140851381 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185066416 | GCTTTCTTTCCTCGC[A/T]TGGTTAACTTTCACT | 6045 |
rs140872183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086791 | GGTTTAAAGTGCTCT[A/G]AAGTAGATTTTTTAA | 6045 |
rs140911411 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185047354 | CCATGCAGACTTTCA[A/G]AATACTGGGAATTTG | 6045 |
rs140931018 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100369 | TATTAAAGATGTACT[A/G]GCATTACTTTTATGG | 6045 |
rs140955188 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185067671 | TGAAAAAAATGCTTT[C/G]TAGGGAAATGGGATA | 6045 |
rs140977509 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091760 | TTGAAAAGAGTTGTT[A/G]TACTAGGTACTTAAT | 6045 |
rs141089080 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185053696 | CTCTCCCATTACTAG[A/G]AGGCAGGGATTTTAA | 6045 |
rs141121261 | snp | A/C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070787 | GGGACTGCAGGTGCC[A/C/T]GCCACCTCGCCGGCT | 6045 |
rs141137953 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185085911 | CCTGCCTTGGCCTTC[C/G]AAAGTGCTGGGATTA | 6045 |
rs141158995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067955 | ACCTCATGATTCACC[C/T]GCCTTGGCCTTCCAA | 6045 |
rs141325669 | snp | A/G | 0.000117388 | 0.00766029 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100202 | TTTTTTGTTTTAGGT[A/G]TTAAATGGCTCTTTT | 6045 |
rs141458589 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185093348 | ATTAAATTTACTTTT[C/T]GAAAAAGGTAAAATA | 6045 |
rs141483444 | in-del | -/GT | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185071723 | CAATGAAGTCACACA[-/GT]GTGTGTGGTTTTGTC | 6045 |
rs141491939 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185081389 | AACTGTAGCCTAATT[C/T]CATCAATTTTTTTTT | 6045 |
rs141508249 | in-del | -/A | 0.0345262 | 0.126772 | intron-variant | RNF2 | GRCh38.p7 | 1:185058196 | CATTTATATTGTATT[-/A]GGTAGTATAGGTAAT | 6045 |
rs141529272 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102727 | ATCAGAATTTCATTC[C/G]TATTTATGGCTGAAT | 6045 |
rs141545513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067116 | GAAAAGATACAATCA[A/G]ATTAGGAATTGATAT | 6045 |
rs141565798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089288 | CTGGTTCCTAACAAG[C/G]CAATACCTGTCCATG | 6045 |
rs141697227 | in-del | -/T | 0.0329836 | 0.124112 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044254 | AAAGAATAATGCTTG[-/T]TTTTCTTTGATGGAT | 6045 |
rs141711732 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185079123 | TTTCTGCCTATGCAG[C/G]TAAAGTTATCTCATT | 6045 |
rs141811524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072015 | GTGGAGACAAAGCTA[C/G]AGATTAATCTGGCAG | 6045 |
rs141899629 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061460 | ACAAGATCACAAAAC[A/C]CCGAATGTGCAGCCT | 6045 |
rs141980782 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079446 | TCAGCCTGAGTCTTC[A/G]TAATAAGGAAGTCCT | 6045 |
rs141992737 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046731 | TAAAAAAATTAAGGC[A/G]TGGTTTCAGTGTTCT | 6045 |
rs141998871 | in-del | -/T | 0.0475351 | 0.146656 | intron-variant | RNF2 | GRCh38.p7 | 1:185077145 | GTAGCCTTTTTGGCA[-/T]TTTTTTTATCTTCAT | 6045 |
rs142025033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185083663 | GTTTTTTGGAGACTC[A/G]AGCTCAGTCTGTTGC | 6045 |
rs142032182 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185080722 | GAAATTCTGGAAATG[C/T]AACTAACTTGTCAAT | 6045 |
rs142105320 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185052726 | AAATGAGGTGACCAT[C/T]GTTTTAGGTGAGCTG | 6045 |
rs142218566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185090854 | GAGATATGTCCTGAA[A/G]TTTTACATTGGAACT | 6045 |
rs142347446 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185054793 | TCCTCCGCCTGCCGG[C/G]GTCAAGCGATCTTGC | 6045 |
rs142378458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058032 | CAGGAGGTTGAGGTG[A/G]GAACATCACCGGAGC | 6045 |
rs142381900 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185080584 | GGTAGCATCCATGTG[A/G]TAGTATTTAAGACTG | 6045 |
rs142442884 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185063782 | GTTACCTGCATTCTA[A/T]TTTGCAGCCCCTTCT | 6045 |
rs142493493 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185086146 | CTACCAAAGCCTCCT[G/T]AACTCCTCAAATTCC | 6045 |
rs142628125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185065636 | CACTCCTGAAGTCAG[C/T]GAGACCACTAACTCA | 6045 |
rs142668963 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101757 | TTTAAATCTTCAGCC[C/T]GGTATGAAAACTTAA | 6045 |
rs142715202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185084489 | GTTTCAGATAGTTTG[A/G]GGGGTTTTGTTTCCC | 6045 |
rs142779479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185088107 | CAGGCAGAGATGCCA[A/G]CTATAGATGATTTTT | 6045 |
rs142812039 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185072750 | TCGAGACCATCCTGG[C/T]TAACACAGTGAAACC | 6045 |
rs142815677 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070058 | ATTCTCAGTAAGTTG[A/G]GGGTAGCTAAATAAT | 6045 |
rs142867393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078317 | TGTCTTTTGCCCCCA[A/G]ATTAGTCTTACTTGA | 6045 |
rs143003126 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043760 | ACTGTTTCTAGAAAG[C/T]GGACTTTCACAAGAA | 6045 |
rs143117823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082291 | GTCGTTGTCAACTTC[C/T]GCTGGCTGGTCACTA | 6045 |
rs143186287 | in-del | -/C | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185077293 | TCTCCCCATCCTCCT[-/C]CCCCCCTCCCTCCTA | 6045 |
rs143228924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051196 | CATTAAACCCTCACT[A/G]TTTACACTGTTTGCT | 6045 |
rs143286766 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185095029 | TTCTGGAGTGTAGTC[A/G]AGATCAAAAACCACT | 6045 |
rs143292461 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185054988 | TACAGGCATGAGCCA[A/G]TGCACCTGCTGTTTC | 6045 |
rs143361528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067504 | AAAGAAAAATGCTAA[A/T]GATTGAGAGAGTTAA | 6045 |
rs143410698 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185053752 | AACAATGTGTGGTAC[A/G]TAATAGGCTCTCAAT | 6045 |
rs143463413 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071529 | CCTTTGGCATCGTGC[A/G]TTTAGAGTCCCGAGA | 6045 |
rs143477508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058768 | CCCTAATGGGCATTT[C/T]GGTATATGTATTTTT | 6045 |
rs143546505 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | RNF2 | GRCh38.p7 | 1:185075656 | GTCCTACATGTCTGG[A/C]GCAGGAGGAAGAGAG | 6045 |
rs143709074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185054107 | GTGTCTAGAAGTGAA[A/G]CTGCCGGGAAAAAGG | 6045 |
rs143816342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061462 | AAGATCACAAAACCC[C/T]GAATGTGCAGCCTTT | 6045 |
rs143934029 | in-del | -/TA | 0.039522 | 0.134904 | intron-variant | RNF2 | GRCh38.p7 | 1:185051832 | TACACACATTTTATG[-/TA]TATATGTATATACAT | 6045 |
rs143953935 | snp | C/G/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185053337 | TTTCCTTTTTTTCTT[C/G/T]TTCTTTTTTTTTTTA | 6045 |
rs143956225 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097041 | GAAGAATGTGGTCTG[G/T]TTCACATCCTAGCTC | 6045 |
rs144018682 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | RNF2 | GRCh38.p7 | 1:185092386 | TTCACTGTGTTGGTC[A/C]GGCTGGTCTTGAACT | 6045 |
rs144078326 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185095855 | CCCTCTAAAGGCTTA[A/G]TATTCACATTCCTCA | 6045 |
rs144110491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094982 | CAGTAATCAGCATCC[A/G]GGCATTTCTGCTTTT | 6045 |
rs144143831 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185048936 | GGGGCGGGGATGGGG[C/G]AGGTGCCTTGGGAGG | 6045 |
rs144143930 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185098820 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAGCCT | 6045 |
rs144217978 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185088216 | AGAGATGAGCAGAGG[A/G]CCTATAACTTCATCC | 6045 |
rs144259528 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185075572 | TCTGCAAGGCTGTAC[A/G]GGAAGCATGGCTGGG | 6045 |
rs144360570 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069223 | TTTGCAAGGCCAAGG[G/T]TGGCGGATTGCTTAA | 6045 |
rs144399604 | in-del | -/TG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095482 | TCCATTCTAGGACTC[-/TG]TAATTCCTTACCCTC | 6045 |
rs144432052 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185076623 | ATGTTAATCCTTCCA[C/G]AATTTTAAAATTCAC | 6045 |
rs144442502 | snp | A/G | 0.000329424 | 0.0128298 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185091665 | TTGTTTGGATATGTT[A/G]AAGAACACCATGACT | 6045 |
rs144496402 | snp | C/T | 0.029116 | 0.117091 | intron-variant | RNF2 | GRCh38.p7 | 1:185056620 | AAGTGATCCTCCCTC[C/T]TTGGCCTCCCAAAGT | 6045 |
rs144496938 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185080392 | GATTTTGGGGCAGGG[G/T]GAATTTAGATTAAAT | 6045 |
rs144621180 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185065042 | GCTGGACTTCTGGGT[C/T]GGGTGGGGACTTGGA | 6045 |
rs144658954 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185046551 | AGATCAATTATAGAC[G/T]CATCTATTTGAAGCC | 6045 |
rs144679344 | in-del | -/G | 0.0244538 | 0.107838 | intron-variant | RNF2 | GRCh38.p7 | 1:185058345 | TCTTCAGAACCCCAT[-/G]GATACTCAGGGAGGA | 6045 |
rs144679399 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185067831 | TTCTCCTACCTCAGC[C/T]TCTCGAGTAGCTGGG | 6045 |
rs144744840 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185049318 | TCACATTATTTCTAG[C/G]ATATGTGCTACATTA | 6045 |
rs144782646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047612 | CATTTCTATACATTA[A/G]CAAAGAAGCATAATT | 6045 |
rs144800885 | in-del | -/TTG | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071393 | ATACGTGACCCTCTA[-/TTG]TTGTGGGAATGTGGC | 6045 |
rs144884694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090364 | TTTGTTAGGCATGTT[A/C]TAAAGAGGCAGAGGA | 6045 |
rs144922433 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185077584 | TTTAAATCTCATATC[C/T]GTACATATGTGTGGT | 6045 |
rs145032432 | in-del | -/TTG | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185076115 | TTTTTTTCCTAGCTA[-/TTG]TTTATCTTTTAAATT | 6045 |
rs145051344 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185046439 | CTGCTGGTCAGAATC[A/G]TTTACCTTCTACAGA | 6045 |
rs145255631 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059638 | TAGCAGTAGTAATAA[C/T]CATATGTTTGGTTGG | 6045 |
rs145378429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080412 | TTAGATTAAATTTAA[A/G]TGAAGATGTATATTG | 6045 |
rs145414081 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF2 | GRCh38.p7 | 1:185067294 | TTTTAGATTGAACTG[C/T]GGAAAGTGGTTTTTA | 6045 |
rs145415168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091341 | GTAAGCTTTTAAATA[A/C]ATTAATATGTTATCT | 6045 |
rs145448541 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | RNF2 | GRCh38.p7 | 1:185048440 | TTTCTATTGCTTAAA[C/T]TTACTTCTCCCATTT | 6045 |
rs145492610 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044547 | AAATGAAGTGCAGAG[C/G]AGCTACGCAATCTAC | 6045 |
rs145512210 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089988 | ATGCAGTGGCGTGAT[C/G]GCGGCTCACTGCAAC | 6045 |
rs145557965 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185053819 | AGTATTAGGTCTTGT[A/G]TGCCTGTGTTTTAAT | 6045 |
rs145695013 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185087496 | ACACATACATTCAGA[C/G]CATAGCACTTCCCTT | 6045 |
rs145728915 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185078212 | AAATCTTGTCACTGC[A/G]TTCCAGCCTGGGTGA | 6045 |
rs145762179 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071213 | GCATTCATCTCAGGG[A/T]AGGCCAAGGGATGAT | 6045 |
rs145774199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185100064 | ATAATGTAAAAAACC[A/G]TAACAGTGTTAAGTG | 6045 |
rs145794257 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RNF2 | GRCh38.p7 | 1:185080867 | TTGATAGTTCCTATT[A/G]ATTTTCCAGGGTAGC | 6045 |
rs145800539 | snp | A/C | 0.046775 | 0.145601 | intron-variant | RNF2 | GRCh38.p7 | 1:185085308 | CGCCCGCCACCGTGC[A/C]CAGCTAATTTTTTGT | 6045 |
rs145952144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185063911 | ACATCGCTTTGTCTG[C/T]CTCTTAAGGACCTTT | 6045 |
rs146175757 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF2 | GRCh38.p7 | 1:185097702 | ACGCCCAGCTAATTA[A/G]AATTTTTTGTTGTTG | 6045 |
rs146295513 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | RNF2 | GRCh38.p7 | 1:185079665 | CTGCTTGTGGTGGCT[A/C]ACGCCTGTAATCCCA | 6045 |
rs146305337 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF2 | GRCh38.p7 | 1:185054835 | CCTGAGTAGCTGGGA[C/T]CACAGGCGGGCGCCG | 6045 |
rs146314617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084009 | TGCAGTGGCACAGTC[A/G]TACCTCACTGAAACT | 6045 |
rs146421916 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | RNF2 | GRCh38.p7 | 1:185060901 | AGGTAGGAAGATCAC[C/T]TGAGGCCAGGAGTTC | 6045 |
rs146480973 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185094999 | GCATTTCTGCTTTTA[A/G]GTTTCCATAGATAAT | 6045 |
rs146519072 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185053614 | CTCCTTGGCCTCTCA[A/G]AGTGCTGGGATTACA | 6045 |
rs146741829 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185091022 | TGTGGAAAAGAATTT[G/T]CGGGGTTCAAAAGTA | 6045 |
rs146883382 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185075726 | TTGTGAGAACTCATT[A/T]ACACGAGAACAGCAA | 6045 |
rs146905474 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101926 | TCAATTCCTTTTCTG[A/G]TGTAATGTTAAAGTT | 6045 |
rs146995081 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185078497 | CATGGCTCCTCTTCT[A/C]CCCCTTGATTGAAGG | 6045 |
rs147029594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185095653 | CTTAAAGTAGTAGCT[A/G]CTCAGTAAATATTTA | 6045 |
rs147045401 | snp | A/T | 0.0150606 | 0.0854603 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101606 | ACAGTATTTAAAAAG[A/T]CATGTTTGCATTGAG | 6045 |
rs147167320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047635 | GCATAATTTCTTCCA[A/G]CAAGAGAAATGAGTT | 6045 |
rs147202987 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185068962 | CTTGACAGTTTTGCT[A/C]AAAATGTTACATTTA | 6045 |
rs147219456 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072225 | GGTGACTGTGAAGAA[C/T]ATCTGGACTCTCATG | 6045 |
rs147310444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069743 | AGAGACATTTTATAA[A/G]TAATTTGCTAATTTC | 6045 |
rs147311305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046816 | CTTTTGGTAATTCCA[A/G]GATGATCAGCTGGAA | 6045 |
rs147326855 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185050692 | GTAAAGTGTTACTTG[A/G]TTTTACAGATAGAAA | 6045 |
rs147383184 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | RNF2 | GRCh38.p7 | 1:185089989 | TGCAGTGGCGTGATC[G/T]CGGCTCACTGCAACC | 6045 |
rs147396769 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF2 | GRCh38.p7 | 1:185073696 | AATGCAGGTAAGACA[A/G]TTACATCAGCCAGTA | 6045 |
rs147485299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069250 | TTAAGCCCAGGAGTT[C/T]GAAACCAGTCTGGGG | 6045 |
rs147501926 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185051766 | TTTCAGAATTTTTTA[C/T]TGAGGTATAACAACT | 6045 |
rs147572940 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043486 | TCCAGATATCCCATA[A/G]GTTTTCCGTTTTTCC | 6045 |
rs147769690 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185080984 | TTAGAAATCCCTCCA[A/G]TGGATTTTTAGAAAT | 6045 |
rs147786309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185085848 | TAGTAGAGACGGTTT[C/T]ACCATGTTGGCCAGG | 6045 |
rs147978894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185072007 | AGGTAGATGTGGAGA[C/T]AAAGCTAGAGATTAA | 6045 |
rs148034073 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185078958 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 6045 |
rs148101368 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185054783 | GCTCACTGCATCCTC[C/T]GCCTGCCGGGGTCAA | 6045 |
rs148153808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063147 | TGTAAATGAGTGAAT[C/T]CTGAGCAATGTCTTT | 6045 |
rs148175628 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185046607 | TCGGAAGTTTTAGAG[A/G]ATGTAACTTTACATT | 6045 |
rs148331333 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185049711 | GAACATTACAGTAAT[C/G]AGAACCTAAGAGCTC | 6045 |
rs148332291 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | RNF2 | GRCh38.p7 | 1:185082583 | TGGTCTTGAACTCCT[G/T]ACCTCAGGTAATCTA | 6045 |
rs148365943 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102309 | GCCATCACTACCAAC[C/T]AGGGTTTCAAAAAGT | 6045 |
rs148383570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185089174 | GTTCTCAATAGGGTT[C/T]GGACTCTTACGAGAG | 6045 |
rs148472951 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF2 | GRCh38.p7 | 1:185065561 | CCACCAGGAGGGCCA[A/G]ACAACTCCAGACGCG | 6045 |
rs148524493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069661 | GACAGCAGTGTGCCT[A/G]GCCTATAATATCTTA | 6045 |
rs148628945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185097544 | GTTTAATAAAGAAAA[C/T]TATTTTTAAGAGATA | 6045 |
rs148645247 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185052098 | ATTATTTTCCTCCTC[C/G]TTTGATCTGACATCA | 6045 |
rs148718683 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185075646 | GAGCAGGCAGGTCCT[A/G]CATGTCTGGAGCAGG | 6045 |
rs148770959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080550 | TGGTCTCAGGATCAA[A/C]TGCTGTACTATCTGG | 6045 |
rs148844860 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071357 | CCTGAAAGATTAAGA[C/T]GAGGGAAGCCATCTT | 6045 |
rs148949992 | snp | C/T | 0.000974538 | 0.0220526 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100256 | ATACTGGAAAGTGAA[C/T]AAACCCATGGAACTT | 6045 |
rs148966197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185053945 | TGGATGTTAGTAACC[C/G]GGATTGAATGTAGCA | 6045 |
rs149035089 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RNF2 | GRCh38.p7 | 1:185078161 | CTGAGGCTGGAGAAT[C/T]GCTTGAACCTGGGAG | 6045 |
rs149035517 | snp | A/C/T | 0.00159649 | 0.0282165 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043616 | AATTGCTTAATCTAA[A/C/T]CACACATCATGATTT | 6045 |
rs149091550 | in-del | -/T | 0.220843 | 0.248294 | intron-variant | RNF2 | GRCh38.p7 | 1:185065942 | AAAAATACTACTTTC[-/T]GCTATACTGTCTCAT | 6045 |
rs149122791 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | RNF2 | GRCh38.p7 | 1:185090692 | TATACCTGCATCTTC[C/G]TTTACAATTCTCGCC | 6045 |
rs149175227 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185095023 | AGATAATTCTGGAGT[A/G]TAGTCAAGATCAAAA | 6045 |
rs149213325 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185067475 | TTACATTTGTGTAAT[A/G]TAACATAAAAGGAAA | 6045 |
rs149233052 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185064468 | TTCAACTTTACAGTG[A/G]TACAAAAGCAATATG | 6045 |
rs149283149 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RNF2 | GRCh38.p7 | 1:185055502 | CTCAGCTCACTGCAG[C/T]CTCCGCCTCCCAGGT | 6045 |
rs149338795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092129 | TCACTGCACCTGGCC[A/G]AGAAATACATTTCCT | 6045 |
rs149355596 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185046508 | TTGATCTCAAACTTT[G/T]AGGTTCATTCCAGTT | 6045 |
rs149391120 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185096632 | AGGCCACCAAGTTAC[A/G]TATTTGTACTTTTGT | 6045 |
rs149514583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082013 | ACCACTGAGCGGGTC[A/G]TCACTAGTTACCAAA | 6045 |
rs149532242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068908 | ACCAGAAAATTTTTA[C/T]GATTAAAGCAGCTGT | 6045 |
rs149655554 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185094757 | ATGGTTTTTAAGACC[C/T]TATATAAGGTGGGCA | 6045 |
rs149672118 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185048081 | CTACCTAATGTGTCT[A/G]CTGGGTCTTCTGGTA | 6045 |
rs149710576 | snp | C/T | 0.00185586 | 0.0304054 | intron-variant | RNF2 | GRCh38.p7 | 1:185099746 | AGTACATTTTTCTCA[C/T]TGGCATATTCTAGAA | 6045 |
rs149830416 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185084880 | GGGCCTATGACTGAA[A/T]AATCAAACTCTGTGA | 6045 |
rs149851529 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070838 | AGACTGGGTTTCACC[A/G]TATTAGCCGGGATGG | 6045 |
rs149886151 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090166 | ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCGA | 6045 |
rs149920581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185059584 | AAAAGTGTCCTGGTT[A/G]CAGCAGACATCTTCA | 6045 |
rs150008001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074443 | CCCTGTCCTGAATCT[A/G]TCTAGGGGCCCACCT | 6045 |
rs150149736 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185087035 | CTGTCAAGTAGTTCA[C/T]ATTTATAAGTGTAAA | 6045 |
rs150161972 | snp | A/G | 1.64866e-05 | 0.00287106 | missense | RNF2 | GRCh38.p7 | 1:185099880 | AACTTCGAAGCAAAG[A/G]TGAATCAAACCAGAT | 6045 |
rs150165078 | in-del | -/TGT | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185064832 | AGCATTATTATTTTA[-/TGT]TGTTGTATATGGAAT | 6045 |
rs150235707 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063333 | TACTGATTCAGTGAG[G/T]CTGAAATGCAACCTT | 6045 |
rs150322414 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF2 | GRCh38.p7 | 1:185077326 | TCTCTCCCTCCCTCT[C/T]TATTTTTTTTCCTAC | 6045 |
rs150412315 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185049898 | CTGCATTTGCTACTG[A/T]CAGGAACTGGAAAGA | 6045 |
rs150448461 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102729 | CAGAATTTCATTCCT[A/G]TTTATGGCTGAATAA | 6045 |
rs150465042 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185055094 | AACTATCACTTTGCA[C/G]ATTGTTTAAATGACT | 6045 |
rs150522383 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | RNF2 | GRCh38.p7 | 1:185094181 | GAGTCTTGCTGTGTC[A/G]CCCAGGCCAGAGTGC | 6045 |
rs150644033 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185079132 | ATGCAGCTAAAGTTA[G/T]CTCATTCAGACTAAT | 6045 |
rs150681005 | in-del | -/GG | 0.0228947 | 0.104514 | intron-variant | RNF2 | GRCh38.p7 | 1:185075639 | AAGGGTGAGCAGGCA[-/GG]GGTCCTACATGTCTG | 6045 |
rs150695049 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084513 | GTTTCCCCCTTCTTA[A/C]TTTTGCAAGAGAATC | 6045 |
rs150711577 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | RNF2 | GRCh38.p7 | 1:185068113 | GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 6045 |
rs150728958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052878 | TGCCTCAAGTAATGA[C/T]GGTGATAATAAGAGA | 6045 |
rs150891152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185089639 | GACAAAAGATGAATA[A/G]GCAGTTCTTCAGAGA | 6045 |
rs150921641 | snp | A/G | 0.000153988 | 0.00877328 | missense | RNF2 | GRCh38.p7 | 1:185098326 | CACTTATGGAAAAAG[A/G]TGACAGTGCACAGAC | 6045 |
rs150961115 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185080662 | AAGGAAGACTAGAAA[A/G]TTCTGCAAAGTCATG | 6045 |
rs150978129 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185066282 | TTTTTCAGCCTCACC[C/G]TGTGCTGAGGCTGTA | 6045 |
rs151033160 | snp | G/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070697 | AGGCTGGAGTGCAGT[G/T]GCGCGATCTCAGCTC | 6045 |
rs151085508 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF2 | GRCh38.p7 | 1:185076725 | ACCCTAAATTCACAT[A/G]TCTGTTTTTGAGCCC | 6045 |
rs151208409 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185058836 | GATTTTTTTAGATAT[C/T]ACTTAAAACGTGCTC | 6045 |
rs151227893 | snp | C/T | 0.00438332 | 0.0466095 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044115 | GCGTGAGCTACCACA[C/T]CCAGCCTTTTTTTCT | 6045 |
rs151264186 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | RNF2 | GRCh38.p7 | 1:185095241 | CCTTGTAAATATTCT[C/T]TTGGTTTTGCTTGTA | 6045 |
rs180751851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068049 | TGCACTGTTGCCCAC[A/G]CTGGAGTGCAATGGT | 6045 |
rs180759812 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084586 | TGGCATGCTGGTCAC[A/C]AAAGGCCATTGCATA | 6045 |
rs180770203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054404 | CGTGTCAAGGCTGGA[C/T]ACTGTGCTCTGTGTC | 6045 |
rs180888908 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102378 | GGAAGAAAAGGCTCA[C/T]CACAAGTGGTGTGAA | 6045 |
rs180898965 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF2 | GRCh38.p7 | 1:185089856 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 6045 |
rs180907594 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081146 | TCAAACACATCTTTA[G/T]TAATCAAAATAGGAA | 6045 |
rs181237238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185083658 | TTTTTGTTTTTTGGA[A/G]ACTCGAGCTCAGTCT | 6045 |
rs181249162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053814 | TAAGTAGTATTAGGT[C/T]TTGTGTGCCTGTGTT | 6045 |
rs181259235 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044687 | GGTTATCTTCTCAAG[A/G]GAACATGACATCTCA | 6045 |
rs181308507 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185067444 | GCTTTAATTAAGGAA[G/T]AAATTATTTGCTCAT | 6045 |
rs181379910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071462 | TACAGCTATCTGTTT[A/G]GGAACAAAAGGAAAG | 6045 |
rs181388403 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058053 | TCACCGGAGCCTGGG[A/C]GGGTTGAGGCTGCAG | 6045 |
rs181394391 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185063997 | CTGTAATTTAATTGT[A/G]TTGGCAAAGTCCATT | 6045 |
rs181420223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073160 | ATGGACATTTCCTAA[A/T]TAGCCATTTTTTTAT | 6045 |
rs181434336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058743 | GTCTAGTTGCTTATA[A/C]GTAGCTTTGCCCTAA | 6045 |
rs181445322 | snp | A/G | 1.64895e-05 | 0.00287132 | missense | RNF2 | GRCh38.p7 | 1:185099871 | CTTTAGAAGAACTTC[A/G]AAGCAAAGGTGAATC | 6045 |
rs181451069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080244 | GTGACTCTCAGATAT[C/T]GTTCATTGAAATCAC | 6045 |
rs181456088 | snp | C/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101289 | AAAAGTTTGTTTCCA[C/T]TGGAAAATTATATCA | 6045 |
rs181476899 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185049239 | ATCAGGATCTCATGC[C/T]ACACTATCAGAGGAT | 6045 |
rs181498338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080738 | AACTAACTTGTCAAT[C/G]ACTCCTAAGTCTTAT | 6045 |
rs181530918 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049655 | ATTTAATATAGGGAG[A/T]TGGTTAGATGAGTGT | 6045 |
rs181580742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075875 | ATATTAGTCATCTTA[A/G]TCTTTGTCAATATCA | 6045 |
rs181669039 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185090556 | CCTTTATGAACAATA[C/G]CTATAGTTTCTATAT | 6045 |
rs181702439 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185063900 | CTTCTCACATCACAT[C/G/T]GCTTTGTCTGCCTCT | 6045 |
rs181753923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061089 | CTGAGCCACTGCACT[C/G]CACTCTGGGTGCTGG | 6045 |
rs181976163 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075421 | CTGCCAAATTGTTCT[C/G]TTCCCCAGAACTTTG | 6045 |
rs181980669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095276 | TCTAGTGGTGGGGCT[A/G]TATGATAGGCACTCC | 6045 |
rs181986833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060669 | GGTCACTAGATTTAA[A/G]TAAATTGGATGAATC | 6045 |
rs181996207 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044539 | GACGAAGAAAATGAA[A/G]TGCAGAGGAGCTACG | 6045 |
rs182048222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058217 | TATAGGTAATCTAGA[A/G]ATGATTTAAAGAATA | 6045 |
rs182091622 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185056533 | CTGGCTCATTTATTT[A/T]TTTTTATTTTTTATT | 6045 |
rs182139793 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185086389 | CAACCCTCTTTCCCA[C/T]ATTTATACTAGATGT | 6045 |
rs182152094 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070581 | ATCCTCAGTTTTTTT[C/T]ACATGAACCTTATTC | 6045 |
rs182225491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185069281 | AACATGGTGAAACCC[C/T]GTCTCTACAAAAAAT | 6045 |
rs182324813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064576 | AACACTTTAAGCTTA[C/T]ATTTTCAACTTACTG | 6045 |
rs182332972 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050766 | TAGGTGATCTAAAAA[A/T]GGGGCTTTGGATTTC | 6045 |
rs182357005 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072680 | ACTGAACAGCTCATG[C/G]CTGTAATCCCAGCAC | 6045 |
rs182409476 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185077396 | TCTCATTTTGCTCCT[G/T]ACTTTTTTAACAGGA | 6045 |
rs182505441 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185055673 | TGATCCATCTGCCTT[A/G]GCCTTCCGAAGTCTG | 6045 |
rs182590128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092123 | CATGAGTCACTGCAC[C/T]TGGCCGAGAAATACA | 6045 |
rs182591638 | snp | C/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185059683 | GCCTTCTCACTCAGA[C/T]CTGGGTTTGAGTCTT | 6045 |
rs182594235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085024 | AGTGGTCCCTGAGTA[A/G]CTGGAACTCAGTGTG | 6045 |
rs182630198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185059001 | AGCTATAAAACTTCT[A/G]CTAGTTTCTGGTTTC | 6045 |
rs182672534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097017 | GTAGGGAGACAGGCA[A/G]TGTGGTAGGAAGAAT | 6045 |
rs182678040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062075 | TAGCAGCAAATATTT[C/T]ACAAGGCTGAGTACA | 6045 |
rs182692392 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092027 | ACGGGGTTTCAACTT[G/T]TTGGCCAGGTTTCAG | 6045 |
rs182693688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052016 | GAAGTGGAACATTCT[A/G]TTACCCAGGAAAGTT | 6045 |
rs182707117 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185073290 | GGTAAATTTCTTTTT[A/C]TTTTTAATTTTTTAA | 6045 |
rs182876014 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185073768 | GCATCTACTTCTGTA[A/G]TCTGTTTCTTCTCAC | 6045 |
rs182907074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056080 | CAGTTGCATTGAAAT[A/G]TAGGTCCCATTTATC | 6045 |
rs182913680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069928 | AGTCTTAAATGAGTA[A/G]TCTTGAATCAGCCAT | 6045 |
rs182972292 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185073978 | TTAAGCCCATGCCTC[A/T]TGTACTTCTGACCAA | 6045 |
rs182986243 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060066 | ACATTGGAACTTGAT[G/T]AACATTTCTCTACCC | 6045 |
rs183103508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097924 | AGACCTTTCAGGAAC[A/G]TGTGGGAAACAATAT | 6045 |
rs183214076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066109 | CTACTGTAGGCCTTT[C/T]TCATCTCTTCAGATT | 6045 |
rs183308862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185051397 | CCTTTCTGAGTCTCT[C/T]TTCTTTTGTTAAAAA | 6045 |
rs183364456 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185081594 | AGACGGGTGGGGTGG[A/G]GGGGGGCGGTTTCAC | 6045 |
rs183431316 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185062817 | GGTAGACCTCCCCCC[A/C]CCCAAAAAAAGGCCA | 6045 |
rs183434633 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185082200 | ATGCTACAACCATAG[A/G]ATGGTAGACATTGAG | 6045 |
rs183453333 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185085432 | TGAGCCACCGCGCCC[A/G]GCCTGACCCTTCTTT | 6045 |
rs183509853 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185064774 | ATGTTTTGTAATTTT[C/T]ATTATGCAAGTCTTG | 6045 |
rs183538834 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185097296 | ATACCATCGCATTTT[C/T]CTCAGTCATTTTGTA | 6045 |
rs183554246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078044 | TGAGGTTTGAGGTTC[A/G]AGACTAGCCCGGCCA | 6045 |
rs183566406 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046162 | TCGCTCCTTCCTTCT[G/T]GGGGGTCGGAGTCGG | 6045 |
rs183582194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047129 | GGTAGCACAGCAAAT[A/G]TGGTCCCTCACTTTT | 6045 |
rs183593939 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185062502 | GGAAACTTGCCCATT[A/G]CATGGAATGGAGTAG | 6045 |
rs183624371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053104 | ACCTAGGCAAGTCAG[G/T]CTCTAGACATTGAAG | 6045 |
rs183692864 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | RNF2 | GRCh38.p7 | 1:185078720 | TTCGAGACCAGCCTG[A/G]CCAACATGGTGAAAC | 6045 |
rs183695733 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185066607 | TAGAGGTTCTCATTT[G/T]CTATCACATGATAGC | 6045 |
rs183698732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072089 | GCTAAGAAGAGGTAG[C/T]ACTGAAATGGTGGCA | 6045 |
rs183701522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185046589 | GTATCTTTTTCGAGG[C/T]TGTCGGAAGTTTTAG | 6045 |
rs183708429 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082645 | CAGGCGTGAGCCACC[G/T]CACCCAGCCTGCAGA | 6045 |
rs183771621 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185089223 | CTGACAGGAGGCAGA[C/G]CTTAGGCAGTAATGC | 6045 |
rs184001119 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093816 | GTACTTTTTATTTCA[A/G]TTTCCCCAACTGTGA | 6045 |
rs184006594 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | RNF2 | GRCh38.p7 | 1:185054003 | TCTACATTCCCCCCC[A/C]ACCCAGTGTTTCTCT | 6045 |
rs184230725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079473 | TCCTCCCTGTTTTAA[C/T]CTTTTAAAGGAAAGC | 6045 |
rs184244526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058112 | GCATTGCTGACAGAG[C/T]GATACCCCATCTCAG | 6045 |
rs184313483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074730 | CAGATTTTTTTTCTC[A/G]TGTCATTATTCTCTA | 6045 |
rs184393912 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185098902 | GACTACAGGCTCATG[A/C]CACCAAGCCCAGCTA | 6045 |
rs184399337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095111 | CCACTCTGTTTACCA[A/C]AGTATAATGTACTAA | 6045 |
rs184401736 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185063296 | GCTGGCTTTTAAACT[A/G]GGGGTGGATGAGGGG | 6045 |
rs184427540 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185060453 | ACTGAAGTTGGTAGT[A/T]TCCCTTGCTCACTTA | 6045 |
rs184538369 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185075046 | TGTCGCCCAGGCTGG[A/G]GTGAGTGGCGTGATC | 6045 |
rs184555316 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185063524 | CATTTTTTGTCACCT[A/T]CTCCCACTCTTACCA | 6045 |
rs184558757 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RNF2 | GRCh38.p7 | 1:185079684 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 6045 |
rs184577947 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043586 | ACAAATCATCACTTT[C/T]CTCAACATCAATTGA | 6045 |
rs184607904 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071069 | GTGAGTATTTGTGTG[C/G]AAATGATGGAATAAA | 6045 |
rs184617626 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185088382 | ACCAACATGGAGAAA[A/C]CCCGTCTCTACTGAA | 6045 |
rs184621980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185057545 | TGTCCCCGTAAGTTT[A/G]CCTTTCCAAGAATGA | 6045 |
rs184715393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185083768 | GTGCCACCACTCCTG[A/G]CTAACATTTTGTATT | 6045 |
rs184833278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048006 | ATAATAGCATTTACA[C/T]AGTCCATTCCTTAAG | 6045 |
rs185035535 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060357 | AGAGTGGCAGTCAAC[A/G/T]GTCAGTAGTAACCTG | 6045 |
rs185036737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092108 | TGCTGGAATTACAGA[C/T]ATGAGTCACTGCACC | 6045 |
rs185102414 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185053277 | CTACATTTATTTTTA[C/T]GTTGATCCACATACT | 6045 |
rs185206423 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185067321 | TTTATGAGGTGTTAC[C/T]GCAGGCAGTGTTATG | 6045 |
rs185234580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185100147 | TTAGTTTCATTTCAT[C/T]ATTATTGTGGTTTGT | 6045 |
rs185284888 | snp | A/G | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185095774 | CTTATGTTGACTTCT[A/G]CATACATTTCAGATT | 6045 |
rs185304984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050098 | GATCTGGACGAATAG[G/T]GTAGGTTAAGATGTA | 6045 |
rs185311295 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185064481 | TGGTACAAAAGCAAT[A/G]TGCATTCAGCATGCT | 6045 |
rs185334668 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185080633 | TTATTGTAATGCAGA[C/G]TTAACAGAAAGATAA | 6045 |
rs185369439 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185069048 | CCTTCTCCCTCATAA[C/G]TACTCTGGTAAGAGT | 6045 |
rs185371628 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185045970 | CTTTCCTCTGCGCGG[A/C]GGCCGGCGCTGCGGC | 6045 |
rs185385888 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185055621 | GGTTTCACCATGTTG[A/G]CAAGGCTGGTCTCGA | 6045 |
rs185447822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084606 | GCCATTGCATATTTG[G/T]TACTTTTTTTCCTTT | 6045 |
rs185726861 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070675 | ACCGAGTCTTGCTGT[A/G]TCACCCAGGCTGGAG | 6045 |
rs185771789 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044608 | TGAACCTAGTTTGCC[C/T]AATTCCCACTGCAGT | 6045 |
rs185780560 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185060678 | ATTTAAATAAATTGG[A/T]TGAATCAGTAGACTG | 6045 |
rs185842669 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185087481 | AGGAATTTTGGTGGG[A/G]CACATACATTCAGAC | 6045 |
rs185850924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057293 | TCTAGCCTGGGCAAC[A/C]CTGTTTCAAAAAATA | 6045 |
rs185863380 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075562 | GGCTCAAGGTTCTGC[A/G]AGGCTGTACAGGAAG | 6045 |
rs185865532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185095394 | ACTACTCTATTTCAG[C/G]AACCTTCTTCCAAAT | 6045 |
rs185923477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058887 | TAGGTCTGTATATTG[A/G]CTTGGTTAAAGTCAT | 6045 |
rs185934668 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185080823 | AACTAATATCTCTAG[A/G]AATATAATACTTCAG | 6045 |
rs185987940 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185090893 | ATTTTGGAGAGAAAC[A/G]TCTTTAGGCATGACA | 6045 |
rs186004188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073246 | CTTATGCATATGCTT[A/G]TTCTATCCCTGTGTG | 6045 |
rs186046015 | snp | A/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101786 | AAAGGTATATATTCA[A/T]TTTTTTACCATTTTA | 6045 |
rs186055574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185073428 | GTAGAGTGACTGTTA[C/T]TCTTTTATTCAGCCA | 6045 |
rs186090135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185097216 | ATAAAGTGCCTTGCC[C/T]GGTAATTAGCTTTAG | 6045 |
rs186098242 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185062327 | AAGCTCATGTTTTAC[A/T]GTTTTCAGATAGACA | 6045 |
rs186177382 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076329 | AGAGTCTCATTCTGT[C/T]GCCCAGGCTGGAGTG | 6045 |
rs186179673 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044712 | ATCTCAACAATAGTA[C/T]ATATAGAGATCAGGG | 6045 |
rs186213786 | snp | C/T | 0.031825 | 0.122064 | intron-variant | RNF2 | GRCh38.p7 | 1:185077641 | TTTTTTTTTTTTTGG[C/T]TAGAAATTTAGCTAT | 6045 |
rs186285609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064603 | ACTGTGGTTTCACTT[C/T]AGACTTAAGATATTT | 6045 |
rs186290213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081331 | GCTTGAAGAAGTGGT[A/G]GTTGGTTGGCGAGAG | 6045 |
rs186292586 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050815 | AGCCAGCAATTTTGA[C/T]AGGCATTCCTTTTGA | 6045 |
rs186311874 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185061443 | CAAACAAAAAAAAAC[A/G]CACAAGATCACAAAA | 6045 |
rs186340742 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102997 | CACCAATGAACAAGC[G/T]TTCTGGCTTTTCCGT | 6045 |
rs186618273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052583 | CTTAATGGGTAAAGA[A/G]TTTTACTTTGGAGTA | 6045 |
rs186620160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066159 | TTGATTTTCTCAGAT[C/T]CATCCTTTACTGTTG | 6045 |
rs186733549 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185055716 | GTGAGCCGCCGTGCC[C/T]GGCCTGTAGTTTCGT | 6045 |
rs186743668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185086516 | TTTGAAATGATGTCA[A/G]ATGGGGAACAATAGG | 6045 |
rs186760346 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070584 | CTCAGTTTTTTTCAC[A/T]TGAACCTTATTCTTT | 6045 |
rs186821181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063901 | TTCTCACATCACATC[A/G]CTTTGTCTGCCTCTT | 6045 |
rs186829462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185056163 | GAGTTCTCCATTACT[C/T]GAAGAGTTCTCCATT | 6045 |
rs186902112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069992 | ATTTTAGTACTTTCA[A/G]TATTTTCTTCTCTAA | 6045 |
rs186911750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086112 | GATAATCTCTTTCTT[C/T]TTAAGGTTTATTTCA | 6045 |
rs186950662 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185069524 | TCTAAGGGCTGAGCT[A/G]TGAGTTCACAGTGAT | 6045 |
rs187011482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073052 | ACACATTTTGCTCTA[C/T]GACTTGCTTTTTTTT | 6045 |
rs187052689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049384 | CTTTTAAAATTATTT[C/T]TCATTTTCTCTCATT | 6045 |
rs187053028 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185082312 | CTGGTCACTATGCTC[C/T]GCGTCTTCAAGGTTC | 6045 |
rs187207194 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185089983 | CTGGCATGCAGTGGC[A/G]TGATCGCGGCTCACT | 6045 |
rs187211983 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185058381 | CTCTGTAATTTTGTG[A/T]GCATGTGCTTTTGTA | 6045 |
rs187486628 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078136 | CCTGTAGTCCCAGCT[A/G]CTTGGGAGACTGAGG | 6045 |
rs187491123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185046312 | TGAGCTTACCCAGGA[A/G]GAGTCGTGGGGGGAG | 6045 |
rs187495975 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185062622 | TGCCATAGAAGAAAA[A/G]TACATTAAAAATATA | 6045 |
rs187569133 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185059225 | CTGAATCCCAGTCTG[C/G]ATTAAAAAAAAAAAA | 6045 |
rs187584647 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185082675 | AACTTCTTTCTTGGA[C/T]CACCACTGCCCTGTA | 6045 |
rs187605250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074596 | AACCAAGGACTAAGA[C/T]CAAATACAAAGAAAA | 6045 |
rs187619214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066713 | AAAGGGACAGAAAGA[A/G]AATAAGGCTGCTGCT | 6045 |
rs187619890 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185060209 | TCTTTAATTCAGATC[C/T]GTGTAAATCTTTTAG | 6045 |
rs187672013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185093496 | CAACTTATTCTATTT[A/C]TTCTCTTTATAGCAA | 6045 |
rs187782343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099112 | GCTGGAGTACAGTGG[C/T]ACAATCTTGGCTGAC | 6045 |
rs187847726 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185078968 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 6045 |
rs187882371 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046646 | ATTTGAAGATGTCAG[A/G]TTTCTTTGAAGTGCC | 6045 |
rs187927815 | snp | A/C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097864 | GTGAATAGAAACATT[A/C/T]GTTAAATTATTTAAA | 6045 |
rs187997712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056559 | TTATTTTTGTAGAGA[C/T]GGGGTTTAGCTATGT | 6045 |
rs188117403 | snp | A/G | 0.000214177 | 0.0103461 | missense | RNF2 | GRCh38.p7 | 1:185098239 | AGCTTGATAATAACA[A/G]TGCAGCAATGGCAAT | 6045 |
rs188144168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063007 | TAGCAGTATTTGTCA[A/G]AATAAAAAAATGTAC | 6045 |
rs188254968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047346 | AATGTAGACCATGCA[A/G]ACTTTCAAAATACTG | 6045 |
rs188257364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063350 | TGAAATGCAACCTTG[A/G]TATCAGAATTGTTTA | 6045 |
rs188447181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089460 | TGGATACCAAGGGTC[A/G]ACCGTATATACTTGG | 6045 |
rs188509934 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065380 | CGAAGGCCCCAGTGG[C/G]AGCCTTCTCTGGTCC | 6045 |
rs188533849 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071151 | TTAGCCTCAGTAAAT[C/G]TATACTTTACATATG | 6045 |
rs188541742 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185088443 | TGCCTGTAGTTGCAG[C/G]TACTTGGGAGGCTGA | 6045 |
rs188550045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057661 | ATTTAGGCTTGAGAA[C/T]TCTTTTTTAGGTAGT | 6045 |
rs188653483 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185073951 | AAGAGACTGCCTCCA[A/C]TTCAGATGCCATTAA | 6045 |
rs188662077 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053181 | ATTTAATCCTTTATT[A/T]AGGAAGGTATTATTG | 6045 |
rs188680723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185067898 | GTATTTTTAATACAG[A/G]TGGGGTTTCACCGTG | 6045 |
rs188686859 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185083858 | GTGATCTACCTGTCT[C/T]GGCCTCCCAAAGGGC | 6045 |
rs188691071 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054205 | TGCTAGGGCACGCAA[C/T]GGGTTTCAATATGCC | 6045 |
rs188773994 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185081609 | GGGGGGGCGGTTTCA[A/C]CATGTTGGCCAGGAT | 6045 |
rs188803245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051516 | AAGCACATGGTAAGT[G/T]TAAGGGGTGTATGTG | 6045 |
rs188808801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087492 | TGGGACACATACATT[C/G]AGACCATAGCACTTC | 6045 |
rs188813177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185057443 | TTGTGGTTCGTTTAT[A/G]AGTTTTTTTTAAGAT | 6045 |
rs188946027 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185092573 | ATTGAAATCGCTGAT[A/T]TTTAGACACTTCATA | 6045 |
rs188948011 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185059700 | TGGGTTTGAGTCTTG[C/G]CTCTGACATTTACTA | 6045 |
rs189102234 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070785 | CTGGGACTGCAGGTG[C/T]CCGCCACCTCGCCGG | 6045 |
rs189105158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095460 | GTATCTGCTTAAGTT[C/T]TCATCTTCCATTCTA | 6045 |
rs189105348 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185075585 | ACAGGAAGCATGGCT[G/T]GGGGAGGCCTCAGGA | 6045 |
rs189113660 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044681 | ATTGCTGGTTATCTT[C/T]TCAAGAGAACATGAC | 6045 |
rs189117766 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185061003 | GAGTCTGTAGTCCTA[C/G]CTGCTTGGGAGGCTG | 6045 |
rs189189736 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185060594 | TTTAGTGTAGAGTTG[A/C]TATGTGTTCAGGACT | 6045 |
rs189200413 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043680 | ATTATGAACACCTGT[C/T]TTCCTTTAATTGAAC | 6045 |
rs189337670 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063626 | TAATTTGAAACAACA[C/G]AAACTTACTATTTTA | 6045 |
rs189341937 | snp | C/G | 0.000785582 | 0.0198034 | intron-variant | RNF2 | GRCh38.p7 | 1:185099742 | TTTAAGTACATTTTT[C/G]TCATTGGCATATTCT | 6045 |
rs189346053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080179 | TGGCCATCCATTCTT[G/T]TTCTTTTCCTCTTTG | 6045 |
rs189350224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185048925 | ACCTTGCATTTGGGG[C/T]GGGGATGGGGGAGGT | 6045 |
rs189356187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185072164 | GGCTGACTCTGAGGT[A/G]CTGGCTAGGGTGGGG | 6045 |
rs189428490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185049477 | TTTAGAGGGTTTCAC[A/G]TTATCCTTTATGAAA | 6045 |
rs189497721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080724 | AATTCTGGAAATGCA[A/G]CTAACTTGTCAATCA | 6045 |
rs189577431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094548 | CATTCAGGCCACAAC[A/C]ATCTTTCATTTGATG | 6045 |
rs189598458 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185060380 | GTAACCTGGATACTG[A/C]CACCACATAAGTATA | 6045 |
rs189648579 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185079519 | AGTCTGCTTTTTGTT[C/T]TGTTTCTGCTTTCTT | 6045 |
rs189652309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058116 | TGCTGACAGAGCGAT[A/T]CCCCATCTCAGATAA | 6045 |
rs189785522 | snp | A/G | 0.000347489 | 0.0131766 | missense | RNF2 | GRCh38.p7 | 1:185100284 | CTTTATTACGCACCT[A/G]CAAAGGAGCACAAAT | 6045 |
rs189791802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063953 | GTGCCAAACCTGGAT[A/G]ATCCAGGATAATCTC | 6045 |
rs189878704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074763 | CAATACCATATAACA[A/G]TTATTTACATAGCGT | 6045 |
rs190002807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185081115 | GACTGTGAATTTTAA[A/G]TAATCAAAACTAGGC | 6045 |
rs190011757 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF2 | GRCh38.p7 | 1:185091809 | TCCAGGGTTTGAGAA[A/G]TACATTTTCTTTTTT | 6045 |
rs190014988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050523 | TTATTCATCTAGATT[A/G]TAAAGACCATTGCTT | 6045 |
rs190018972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064501 | TTCAGCATGCTCCTT[A/G]ACTTGTGATGGGGCT | 6045 |
rs190028030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185073254 | TATGCTTATTCTATC[C/T]CTGTGTGAGAATTTG | 6045 |
rs190039039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058979 | GTGCTAATTTTAGAT[G/T]TATCAGAGCTATAAA | 6045 |
rs190171207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070260 | CACTTTGCAGATTAA[A/G]AAAAAGCCTTAAGAG | 6045 |
rs190177518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086239 | GATTGTTGTTTATCT[A/G]TTTGCATGCATTTCC | 6045 |
rs190182989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067338 | CAGGCAGTGTTATGA[C/T]GGCAGTTGGATTGCT | 6045 |
rs190188348 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056363 | TCTTTTTTTTTTTTT[C/T]CTCATTTTTTTTAGA | 6045 |
rs190328554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185075291 | GAGCTACTGTATTGT[A/G]TATTTCTTACAGCAT | 6045 |
rs190416462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083016 | AGAAGCTGGCCATCT[A/G]TATTTATACATGGTT | 6045 |
rs190425346 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185053537 | TTTTCTTTATTTTTG[G/T]AGAGATCGGGGTCTC | 6045 |
rs190481728 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185090186 | CGGCCTCCCGAAGTG[C/T]TGGAATTACAGGTGT | 6045 |
rs190561363 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095136 | TACTAAATGTTAAAT[A/G]TATTTATTTTTAGAA | 6045 |
rs190631260 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185073636 | GTTAAAATGCATATT[A/G]TACTGTGGTTCTAAG | 6045 |
rs190868318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185092121 | GACATGAGTCACTGC[A/G]CCTGGCCGAGAAATA | 6045 |
rs190874656 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185059562 | AATTGTTATATTTAA[C/T]GACTGGAAAAGTGTC | 6045 |
rs190942639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185077968 | GACAAGTAAGGGGCC[A/G]GGCGTGGTGGCTCAC | 6045 |
rs190948291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185084647 | GCTTCTCTTAGCTGT[A/G]TTATCTTTGATGTGC | 6045 |
rs190950341 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046130 | GGGGGTGGGGTAGGG[A/G]GCACTTTGTGCAGAT | 6045 |
rs190952487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062387 | ATGTGTATATATTCA[A/C]ATATACACATATTTC | 6045 |
rs191086194 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103070 | TAACTATATTAATGG[A/G]TATCCTTATGATAGC | 6045 |
rs191101040 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185066381 | TGTACCTTTCCTTAT[G/T]ATGTTGGTCCTTCAG | 6045 |
rs191109111 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185082414 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 6045 |
rs191112709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185064664 | CCCCATGTAGGTCAA[C/T]GAGCATCTTTATTGT | 6045 |
rs191113214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052913 | TGTACTACAGCTACA[A/G]TGCTTAATATGAGCC | 6045 |
rs191117950 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081582 | TATTTTTAGTAGAGA[C/T]GGGTGGGGTGGGGGG | 6045 |
rs191174506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185081766 | AGCATTGTTGTGGAT[A/G]AGAATTGGGCCCTTT | 6045 |
rs191274306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095956 | GTAGTATTATAGACG[C/T]GATTTGATAAATGTA | 6045 |
rs191276268 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185062021 | GCTTACTCCTGTTTC[A/G]GTAACCAGTATTCCT | 6045 |
rs191330396 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065971 | ATTTTTTTTTTTTTA[C/G/T]TATCAGCATCTACAC | 6045 |
rs191432486 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045085 | GTGAAGTTCTGCAAA[C/T]CAAAGCCTGATGAGG | 6045 |
rs191496272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077142 | ACTGTAGCCTTTTTG[A/G]CATTTTTTTTATCTT | 6045 |
rs191675444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085429 | GCGTGAGCCACCGCG[C/T]CCGGCCTGACCCTTC | 6045 |
rs191745059 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185093718 | CCTTCTCTTTGAATA[A/G]TTTTCTTCACCTGGC | 6045 |
rs191749729 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185069537 | CTATGAGTTCACAGT[A/G]ATCCAGCACATGCTA | 6045 |
rs191766551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074608 | AGACCAAATACAAAG[A/G]AAAAAAAAGACCAGA | 6045 |
rs191780284 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RNF2 | GRCh38.p7 | 1:185060214 | AATTCAGATCTGTGT[A/G]AATCTTTTAGCTTTG | 6045 |
rs191873340 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF2 | GRCh38.p7 | 1:185088586 | CTAAAGGAAGTATTT[C/G]AAGGAGGATGTAGTT | 6045 |
rs191918965 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055624 | TTCACCATGTTGGCA[A/C]GGCTGGTCTCGAACT | 6045 |
rs191960037 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185097865 | TGAATAGAAACATTC[A/G]TTAAATTATTTAAAT | 6045 |
rs191969081 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058692 | TTTCTCTTTTTAATA[C/T]TGATTATTTGAAGAA | 6045 |
rs191973056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057464 | TTTTTAAGATTTGTA[G/T]TTATGTTCATGATAA | 6045 |
rs191983767 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062721 | ACACTCATGACAGAC[A/G]AAAGGTCAATTTCCT | 6045 |
rs191992477 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RNF2 | GRCh38.p7 | 1:185078544 | TAAAGTATCAGCATT[A/G]GTAAGCAGTAATTCT | 6045 |
rs192038745 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055970 | TTTCCTCAAATAATT[G/T]TAAAGTAATGTATGT | 6045 |
rs192146367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185075028 | TGAGATGGAGCCTTG[C/T]TCTGTCGCCCAGGCT | 6045 |
rs192214610 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185069117 | CTCTTTTGCCTGTTA[A/T]TGTGCTATTTATTAT | 6045 |
rs192277636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097221 | GTGCCTTGCCCGGTA[A/G]TTAGCTTTAGTATCT | 6045 |
rs192385683 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185073151 | TTCTATACTATGGAC[A/G]TTTCCTAATTAGCCA | 6045 |
rs192399389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051230 | TAGAGTCTTATTCAG[G/T]CTGGGACGGCTGTCT | 6045 |
rs192460765 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185079622 | ATGTTGTCCAATTCC[A/C]GGAGCCCAAATAAAA | 6045 |
rs192463935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185099140 | GACTGCAACCTTTGC[C/T]TCCCGAGTTCAAGCG | 6045 |
rs192480072 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185063508 | AATAAACCGAAGTTC[A/G]CATTTTTTGTCACCT | 6045 |
rs192521015 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185060417 | TGTTTAGAGGTTCCT[A/G]TTATCTGAGTAGGGA | 6045 |
rs192559608 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185073952 | AGAGACTGCCTCCAC[G/T]TCAGATGCCATTAAG | 6045 |
rs192574744 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185059701 | GGGTTTGAGTCTTGC[C/G]TCTGACATTTACTAT | 6045 |
rs192607374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095006 | TGCTTTTAAGTTTCC[A/G]TAGATAATTCTGGAG | 6045 |
rs192643631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051858 | ATACATATTATATAT[A/T]CATGCATATATATAT | 6045 |
rs192733049 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063201 | ATGCCAGATGTTTCT[C/T]AGGTCACTGAAACAG | 6045 |
rs192767707 | snp | C/T | 0.000399281 | 0.0141238 | missense | RNF2 | GRCh38.p7 | 1:185098242 | TTGATAATAACAATG[C/T]AGCAATGGCAATTGA | 6045 |
rs192804880 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070786 | TGGGACTGCAGGTGC[C/G]CGCCACCTCGCCGGC | 6045 |
rs192823799 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF2 | GRCh38.p7 | 1:185046384 | AACCGTGTCGTTTAC[A/G]CTGAGATGCTAGTAC | 6045 |
rs192946930 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185047023 | ATTTCTACTTTTCAC[A/G]ATCAACAAGTATCTT | 6045 |
rs192982317 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079417 | TCAGTTTTCTAGAAA[A/G]TAGGAGATTATAGTC | 6045 |
rs193016223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185087977 | TGCTGTAATAAGTAC[C/T]GATAAGGCACCAAGG | 6045 |
rs193056639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057126 | CAGCCTGGGCAACAT[A/G]ATGAAACCCTGTCTC | 6045 |
rs193091312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185087074 | GTTTTTCTTCTTTTT[A/C]ATTTTTGAGAACCAG | 6045 |
rs193114778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092863 | TTCGACGAGTGGTAT[A/G]GAGGGTTTGAGGTTT | 6045 |
rs193136229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185066980 | TTTCCTTGTAAGACA[A/G]CTTAGTTATAGAGAG | 6045 |
rs193252032 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070669 | TTTGAGACCGAGTCT[C/T]GCTGTGTCACCCAGG | 6045 |
rs193267480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053202 | GGTATTATTGTTATT[A/G]TTCCCATAAAAAAAT | 6045 |
rs193284878 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185082873 | CGTTAGCAAAAAAAC[A/G]TAAAGTGAGAAATGC | 6045 |
rs199568911 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077639 | TGTTTTTTTTTTTTT[G/T]GCTAGAAATTTAGCT | 6045 |
rs199593640 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091953 | CAGAGTAGCTGGGAT[-/A]TACAGGCATTGCCAC | 6045 |
rs199650388 | snp | A/G | 0.00199792 | 0.0315431 | missense | RNF2 | GRCh38.p7 | 1:185098097 | GGCAAGAAACAACAG[A/G]TTGAAAATGGTAGTG | 6045 |
rs199801845 | in-del | -/AAAT | 0.0483699 | 0.147802 | intron-variant | RNF2 | GRCh38.p7 | 1:185057304 | CAACCCTGTTTCAAA[-/AAAT]AAATAAATAAATAAA | 6045 |
rs199834920 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059296 | ATCTACCTATGTGAC[-/G]GGGGGACACAGGAAA | 6045 |
rs199842890 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051747 | TTCTTTTTTTTTTTT[A/C]ATCTTTCAGAATTTT | 6045 |
rs199899099 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185057508 | TCATGTGGCGGTGGG[C/T]TGGAAGTAAAGCAGT | 6045 |
rs199992185 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081601 | TGGGGTGGGGGGGGG[-/C]GGTTTCACCATGTTG | 6045 |
rs200062271 | in-del | -/AT | 0.0387552 | 0.1337 | intron-variant | RNF2 | GRCh38.p7 | 1:185051864 | ATTATATATACATGC[-/AT]ATATATATGTAAAAA | 6045 |
rs200104377 | in-del | -/C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100554 | TGTGTTTTTTTTTTT[-/C/T]CCCCACAAAGTGTGT | 6045 |
rs200112640 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062706 | AACTGGGGAAAATTA[A/T]CACTCATGACAGACA | 6045 |
rs200133076 | in-del | -/TTGTT | 0.0345262 | 0.126772 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043821 | ATTTTGTTGTTGTTG[-/TTGTT]TTGTTTTGTTTTGAG | 6045 |
rs200238996 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082740 | CGATGTTGCGAGTAG[C/T]CTCCACTGCTTTACG | 6045 |
rs200349054 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | RNF2 | GRCh38.p7 | 1:185065985 | AGTATCAGCATCTAC[G/T]CAGCCACAAGCTTAG | 6045 |
rs200353183 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095507 | ACCCTCCCTGCCTCA[-/T]TTTTTTTCCCATAGC | 6045 |
rs200385213 | snp | A/G | 0.000182441 | 0.0095492 | intron-variant | RNF2 | GRCh38.p7 | 1:185091777 | ACTAGGTACTTAATT[A/G]TACCACGAAAGTGCT | 6045 |
rs200393372 | snp | G/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044228 | GTAGGCAAAAGCTTT[G/T]AAGCCACTGAAAAAG | 6045 |
rs200496846 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064094 | ATTCACACTGCCATA[A/G]TTAGAGACTTAATTC | 6045 |
rs200605982 | in-del | -/TATC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095667 | TGCTCAGTAAATATT[-/TATC]TATGTGTGAATTTTT | 6045 |
rs200612317 | in-del | -/A | 0.304305 | 0.244031 | intron-variant | RNF2 | GRCh38.p7 | 1:185049671 | TGGTTAGATGAGTGT[-/A]AAAAAAAAAAAGCGG | 6045 |
rs200657857 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062765 | CTTACAAGTTAACTT[-/A]AAAAAAAAAACCTGA | 6045 |
rs200658900 | snp | A/C | 0.00199793 | 0.0315432 | intron-variant | RNF2 | GRCh38.p7 | 1:185099784 | TTTTAATGATTTATT[A/C]TTCTAGATACATAAA | 6045 |
rs200675534 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095816 | TTTACAAATATTTTT[A/T]TGTAGGTATATGTTC | 6045 |
rs200736851 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076809 | TTCTATTAAGCTTTA[A/G]TGTTTGTTTTAAGGT | 6045 |
rs200819165 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064686 | CTTTATTGTTATCTT[A/C]ATAATATTTTGTCTT | 6045 |
rs200880282 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054953 | GTCCGCCTGCCTCGG[-/G]CCTTCCAGAGTGCTA | 6045 |
rs200996342 | in-del | -/A | 0.0463947 | 0.145069 | intron-variant | RNF2 | GRCh38.p7 | 1:185059227 | AATCCCAGTCTGGAT[-/A]TAAAAAAAAAAAACC | 6045 |
rs201002815 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090820 | CCAAGTAGGATTCAC[-/T]AATCATTCTGCAGCA | 6045 |
rs201088676 | snp | A/G | | | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098159 | CAGTAATGCATCCAC[A/G]CATAGCAATCAGGAA | 6045 |
rs201206529 | snp | A/G | 4.98235e-05 | 0.00499092 | intron-variant | RNF2 | GRCh38.p7 | 1:185099976 | CTGTGAGTATTTAAA[A/G]TAATAGACTGTTGAA | 6045 |
rs201213255 | in-del | -/TTTT | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100544 | CTGAAGTTTCTTGTG[-/TTTT]TTTTTTTCCCCACAA | 6045 |
rs201249554 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061552 | TGCAATTATGGCAGG[G/T]GGATGTGGAGAAGTA | 6045 |
rs201377412 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094131 | CAGTTTTTTTTTTTT[-/T]ATTTTTTTTATTTTT | 6045 |
rs201402005 | snp | C/T | 0.00199799 | 0.0315437 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185099953 | AGCAACAGCCAGTGG[C/T]CAGTTCACTGTGAGT | 6045 |
rs201413941 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048777 | GTAGTAAAAAAAAAA[-/A]TCATGCTTGAAAATC | 6045 |
rs201415989 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085145 | CCCTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs201420664 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091819 | GAGAAATACATTTTC[-/T]TTTTTTTTTTTTTGA | 6045 |
rs201508156 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093238 | GCAAGCACTCAGTCA[C/T]AGCATTGAGGAAGGA | 6045 |
rs201556991 | snp | C/T | | | missense | RNF2 | GRCh38.p7 | 1:185098154 | CACTGCAGTAATGCA[C/T]CCACACATAGCAATC | 6045 |
rs201614864 | in-del | -/TC | 0.00676609 | 0.0577691 | intron-variant | RNF2 | GRCh38.p7 | 1:185064147 | AATGGAATATTTCAA[-/TC]TGTCTTAAATTTATA | 6045 |
rs201627494 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079943 | CAGAAAAAAAAAAAA[-/G]CCAATTGTGTCTTTA | 6045 |
rs201683390 | snp | C/T | 0.000312976 | 0.0125056 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087577 | GGCTGTGCAGACAAA[C/T]GGAACTCAACCATTA | 6045 |
rs201726589 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061326 | TAGAGACGGGGTTTC[A/T]CCATGTTAGCCAGGA | 6045 |
rs201748714 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051746 | ATTCTTTTTTTTTTT[C/T]CATCTTTCAGAATTT | 6045 |
rs201772219 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064687 | TTTATTGTTATCTTA[A/T]TAATATTTTGTCTTC | 6045 |
rs201995249 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085405 | CCTCCCAAAGTGCTG[A/G]GATTACAAGCGTGAG | 6045 |
rs202011907 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185100186 | CATAATTTTTTCTTT[C/T]TTTTTTGTTTTAGGT | 6045 |
rs202081769 | snp | A/G | 0.000148379 | 0.00861205 | missense | RNF2 | GRCh38.p7 | 1:185099874 | TAGAAGAACTTCGAA[A/G]CAAAGGTGAATCAAA | 6045 |
rs202160812 | snp | A/T | 0.0898829 | 0.191996 | intron-variant | RNF2 | GRCh38.p7 | 1:185059228 | AATCCCAGTCTGGAT[A/T]AAAAAAAAAAAACCT | 6045 |
rs202214810 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083419 | AGAAGACAGGCTGGG[G/T]TTTTATTATACTAAC | 6045 |
rs202237786 | snp | G/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101855 | TTTTTTTTTTTTTTT[G/T]TAATCTGTGCCATGA | 6045 |
rs202239334 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076862 | AAAATACTCTGGGCA[-/T]TTTTTTTTTGCATCC | 6045 |
rs207460762 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058916 | ATGTTGATTTCCAGT[A/G]TATATGAAGTGTGCC | 6045 |
rs367585015 | in-del | -/ATA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064690 | ATTGTTATCTTAATA[-/ATA]TTTTGTCTTCAAATC | 6045 |
rs367601361 | snp | C/T | 0.420733 | 0.18262 | intron-variant | RNF2 | GRCh38.p7 | 1:185079079 | ATGACTAGATCTTTT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs367648508 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069719 | GGAGCTAGGGAGGAG[A/G]GTAATCCAAGAGACA | 6045 |
rs367768736 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084727 | ATTGTGCCATCTAGC[C/T]TACTAAGCGCAATAA | 6045 |
rs368038035 | snp | A/G | 0.000173229 | 0.00930508 | intron-variant | RNF2 | GRCh38.p7 | 1:185098383 | ATTATCTAAATTCAG[A/G]ATGTTTAATTTGGAG | 6045 |
rs368144060 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061391 | AAAAAGGGAAACAGA[A/C]ATGAAAGCTTCTGAT | 6045 |
rs368144564 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058212 | GGTAGTATAGGTAAT[C/T]TAGAGATGATTTAAA | 6045 |
rs368160330 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049548 | TTCAGTGAAGCAACA[A/G]GATATCTGAGAGCAG | 6045 |
rs368232686 | in-del | -/GT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074998 | TGTGTGTGTGTGTGT[-/GT]TATTTATTTATTTTT | 6045 |
rs368316726 | snp | A/C | 0.000119598 | 0.00773205 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100330 | AATTCTGAGACTGAA[A/C]TTTTTTATAGCCTAT | 6045 |
rs368423981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185075997 | TTATGTATTGTGTTA[A/T]TTACTCATCATTTTG | 6045 |
rs368481504 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095869 | AATATTCACATTCCT[C/T]ATTTCTTTTTTGTTC | 6045 |
rs368800863 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081578 | TTTGTATTTTTAGTA[G/T]AGACGGGTGGGGTGG | 6045 |
rs368811125 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071035 | GCATAAGTATACTTT[A/G]TTTGCCAAGTAATAC | 6045 |
rs368940635 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | RNF2 | GRCh38.p7 | 1:185064869 | TTTTAATTTCCTTTT[C/T]AGGTTGTTCATTGTT | 6045 |
rs368960084 | snp | C/T | 9.909e-05 | 0.00703812 | intron-variant | RNF2 | GRCh38.p7 | 1:185087686 | ATGAGACGTGTAAAC[C/T]GGGATACATTTTTAG | 6045 |
rs368972499 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094813 | CTCTCTGACATTATC[A/G]TCTGATTTATTCAGG | 6045 |
rs368988154 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044889 | CACTGGAAGGGGCCA[A/G]GGAGGTAGGAATAAA | 6045 |
rs369037327 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071256 | TCCTTGTCTTCTACC[C/T]GTGAAGATAAGCTGG | 6045 |
rs369091605 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065637 | ACTCCTGAAGTCAGC[G/T]AGACCACTAACTCAC | 6045 |
rs369213965 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054480 | AGGCCTTCTTCTCCC[A/G]TCTGGGTCTCTGGCC | 6045 |
rs369221497 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185083510 | TCTTCGCTTTCTCTC[C/T]CCTTCCCACTCAGGG | 6045 |
rs369266899 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064257 | ATTTCTACTTTATTC[A/T]TAGGAATGTAGGTTG | 6045 |
rs369268106 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079093 | TCTTTTTTTTTTTTT[-/TT]CGGATTTATTTTGTT | 6045 |
rs369326634 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060109 | CAATCTTGGAATATA[C/T]CACTTTGCAGAAGCT | 6045 |
rs369389423 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185085452 | GACCCTTCTTTCTTA[A/C/T]ACCAGTGTTTTGTAT | 6045 |
rs369442858 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081751 | TGTGACGTGCATTTG[A/T]GCATTGTTGTGGATA | 6045 |
rs369488899 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059154 | GAGAAGAGAGAGATT[A/G]AGTTAGTCTACCTTT | 6045 |
rs369585492 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052082 | ACCTGTGACACCCCC[A/C]ATTATTTTCCTCCTC | 6045 |
rs369667956 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087482 | GGAATTTTGGTGGGA[C/T]ACATACATTCAGACC | 6045 |
rs369765963 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059454 | ATCACCTTCTAGAAC[A/G]TAACTTTTACGTAGC | 6045 |
rs369825467 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044987 | AGGTCATTTTCCCAG[A/G]AGCAATTACACTTGC | 6045 |
rs369837041 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053935 | CATTCTTGGATGGAT[A/G]TTAGTAACCCGGATT | 6045 |
rs369869181 | snp | A/G | 0.000132589 | 0.00814105 | intron-variant | RNF2 | GRCh38.p7 | 1:185091774 | TATACTAGGTACTTA[A/G]TTGTACCACGAAAGT | 6045 |
rs369872635 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093121 | ATCACTAAGGCCAGA[C/T]CCAAACTTTGATGCA | 6045 |
rs369944892 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058307 | AATATCTGTGGCTTT[C/T]GGTGTCTGTGGTGTG | 6045 |
rs369958171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085288 | CCAATAACTGGGACT[A/G]CAGGCGCCCGCCACC | 6045 |
rs369972542 | snp | C/T | 0.000131785 | 0.00811635 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185091671 | GGATATGTTGAAGAA[C/T]ACCATGACTACAAAG | 6045 |
rs370038127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078783 | GGCGTAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 6045 |
rs370095160 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095387 | TACTTACACTACTCT[A/G]TTTCAGGAACCTTCT | 6045 |
rs370098836 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065473 | CTTTGGGTCGGCACT[A/G]CTACCTTTATGAGCT | 6045 |
rs370247186 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185098429 | GTATAAGAAGTAGGA[A/G]CAATATTTGTCATCC | 6045 |
rs370317006 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089002 | GATGATTTAAAGCAG[C/T]AGTCCCCAGGGACCA | 6045 |
rs370498977 | in-del | -/TAG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056875 | AGGAAATTGAAGAAG[-/TAG]GAAAAAATGCTTTTG | 6045 |
rs370623118 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092851 | CAAATTTTTTCTTTC[A/G]ACGAGTGGTATAGAG | 6045 |
rs370708173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185074428 | CTCCTGAAAACCAGT[C/T]CCTGTCCTGAATCTA | 6045 |
rs370715628 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069705 | TTGGGTATGTGTTTG[C/G/T]AGCTAGGGAGGAGGG | 6045 |
rs370772164 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081592 | AGAGACGGGTGGGGT[-/G]GGGGGGGGCGGTTTC | 6045 |
rs370826982 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079079 | TGACTAGATCTTTTC[-/TT]TTTTTTTTTTTTTTT | 6045 |
rs370878139 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048856 | GTTGGAACACATTGC[A/T]GTTTCTTGGTGTTTC | 6045 |
rs370878832 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185081957 | TTGGTGCATGTTTGC[C/T]GTTGGGAAGTGCTTT | 6045 |
rs371001225 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075015 | ATTTATTTATTTTTG[A/G]GATGGAGCCTTGCTC | 6045 |
rs371061326 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073825 | TTTTTGCTACACTAA[A/C]AATTCTCCAACTCTT | 6045 |
rs371064337 | snp | A/G | 1.65671e-05 | 0.00287807 | intron-variant | RNF2 | GRCh38.p7 | 1:185091767 | GAGTTGTTATACTAG[A/G]TACTTAATTGTACCA | 6045 |
rs371088814 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062301 | GACAGTGTAGGAAGT[G/T]ATAGTGTATTAAGCT | 6045 |
rs371198643 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053447 | TCAAGTGATCCTCCC[A/G]CCTCAGCCGCCTTTG | 6045 |
rs371427328 | in-del | -/TG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061788 | TCAGGAGAACAAGAC[-/TG]TTTTTAGGCAATGTA | 6045 |
rs371461250 | snp | A/G | 1.84848e-05 | 0.00304008 | intron-variant | RNF2 | GRCh38.p7 | 1:185093303 | AGAGGGTCAGAGAGG[A/G]TAGCTGTTTTTCTGA | 6045 |
rs371468038 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086520 | AAATGATGTCAAATG[G/T]GGAACAATAGGAGGA | 6045 |
rs371510480 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058725 | CACATTAAGATTATC[A/G]AAGTCTAGTTGCTTA | 6045 |
rs371510671 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084944 | AGGAATGAGGGACAT[C/G]TTGTGTCTTCAGGGA | 6045 |
rs371541316 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077818 | TTCTAATGCCTGATT[C/G]ATTGTTTTTTTTCAG | 6045 |
rs371564301 | snp | A/G | 3.51964e-05 | 0.00419487 | intron-variant | RNF2 | GRCh38.p7 | 1:185098391 | AATTCAGAATGTTTA[A/G]TTTGGAGGTAAAAGG | 6045 |
rs371652713 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053364 | TTTAAGAGACAGGAT[C/T]TTGCTATGTTGCCCA | 6045 |
rs371885887 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094102 | CAATTCCATCATTCT[A/G]CTTGCTTAAGCCAAA | 6045 |
rs371900272 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083964 | AAAAAAAATTAGGGG[G/T]GGGATCTCACTCTGT | 6045 |
rs371908213 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185052420 | CTGACACATGTTACA[A/G]TGTGGATGAACCTTG | 6045 |
rs371934419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070837 | GAGACTGGGTTTCAC[C/T]GTATTAGCCGGGATG | 6045 |
rs371994065 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185084559 | TTTCAAGTCAGTTTT[A/G]TTTTGAGACCTTGGC | 6045 |
rs372003275 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051618 | AGTTGTTGAGTTTCT[A/G]TATTTAAAAAAGTGT | 6045 |
rs372005955 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058365 | CTCAGGGAGGACTGT[A/G]CTCTGTAATTTTGTG | 6045 |
rs372017852 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096493 | ACTGTCATTCTACTT[C/T]GTTTTATGAATTTGA | 6045 |
rs372033695 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044254 | AAAAGAATAATGCTT[C/G]TTTTCTTTGATGGAT | 6045 |
rs372043337 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045450 | CTCGCTCGCTCCTTC[C/T]CGCCCTCCCCGCAGC | 6045 |
rs372204033 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185055808 | TTGGAAGTTATATCT[A/G]TTGTTTAGTTTTATG | 6045 |
rs372206490 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081601 | TGGGGTGGGGGGGGG[C/T]GGTTTCACCATGTTG | 6045 |
rs372237810 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087606 | TAAGCAAAACATGGG[A/G]ACTCAGTTTATATGA | 6045 |
rs372241396 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064973 | CAGTTTTGTGTGTAT[A/G]TGTGGAGTCTTCAGG | 6045 |
rs372291857 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049671 | TGGTTAGATGAGTGT[A/T]AAAAAAAAAAAGCGG | 6045 |
rs372369277 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044892 | TGGAAGGGGCCAAGG[A/G]GGTAGGAATAAAGCA | 6045 |
rs372369646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185078108 | AGAAATTAGCCAGGT[A/G]TAGTGGTGTGTGCCT | 6045 |
rs372613037 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059489 | CTTGTAGCGCAGATG[C/T]AAATTAGTGTTATCT | 6045 |
rs372636643 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054794 | CCTCCGCCTGCCGGG[A/G]TCAAGCGATCTTGCC | 6045 |
rs372638907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185090658 | AGGAAGCACGGGAGC[A/G]TATTGAAAGCCACTT | 6045 |
rs372646484 | snp | C/T | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071591 | CCAGGATGTACTTGT[C/T]AAAGAGTTACTCTGC | 6045 |
rs372665414 | snp | A/G | 1.65121e-05 | 0.00287329 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091588 | TTACAGGAGGCAATA[A/G]CAGATGGCTTAGAAA | 6045 |
rs372720129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072711 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCATGAGG | 6045 |
rs372740771 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089924 | TAATCCCAGCTACTC[G/T]GGAGGCTTTTTTTTT | 6045 |
rs372825302 | snp | A/G | 1.71814e-05 | 0.00293094 | missense | RNF2 | GRCh38.p7 | 1:185093269 | CTGAAGATACAGGCC[A/G]TGAACAGGTATATGG | 6045 |
rs372834423 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062824 | CTCCCCCCCCCCAAA[A/T]AAAGGCCAATAAAGC | 6045 |
rs372875470 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079942 | TCAGAAAAAAAAAAA[-/A]GCCAATTGTGTCTTT | 6045 |
rs372888810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185072406 | GGTATTGGGGATATT[A/G]TGGTAAATAAGAGAT | 6045 |
rs372957574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071387 | TGGGAGATACGTGAC[C/T]CTCTATTGTTGTGGG | 6045 |
rs373023574 | snp | G/T | 1.6577e-05 | 0.00287893 | intron-variant | RNF2 | GRCh38.p7 | 1:185091776 | TACTAGGTACTTAAT[G/T]GTACCACGAAAGTGC | 6045 |
rs373070208 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046219 | CCTCGGGGTTCCTCG[A/G]GGAGACCCCTTCAGC | 6045 |
rs373207635 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065955 | TCTGCTATACTGTCT[A/C]ATTTTTTTTTTTTTA | 6045 |
rs373234473 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086908 | AAAAATATTTATTGT[A/T]TTGGGTTAAGACAAT | 6045 |
rs373413556 | snp | A/G | | | missense | RNF2 | GRCh38.p7 | 1:185098262 | ATGGCAATTGATCCA[A/G]TAATGGATGGTGCTA | 6045 |
rs373435775 | snp | G/T | 0.000940309 | 0.0216626 | intron-variant | RNF2 | GRCh38.p7 | 1:185100149 | AGTTTCATTTCATTA[G/T]TATTGTGGTTTGTGC | 6045 |
rs373586546 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083608 | ACTACAGGCCAACCC[-/T]ATTTTTCTTACTCTA | 6045 |
rs373599858 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073694 | GGAATGCAGGTAAGA[C/G]AATTACATCAGCCAG | 6045 |
rs373605916 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051462 | TTATTTGAAAAGATA[A/T]AAGAAGTAATGTACG | 6045 |
rs373679384 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099290 | TGACCTCAAGTGATC[C/T]ACCTGCCTCAGCCTC | 6045 |
rs373704731 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091981 | ACCGTGGCCGGCTAG[-/T]TTTTTTTTTTTTTTT | 6045 |
rs373713697 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075759 | GGGAAATCCACTCCC[A/G]TGATCCAGTCACCTC | 6045 |
rs373758464 | snp | A/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045074 | CCGAAGTTCATGTGA[A/C]GTTCTGCAAACCAAA | 6045 |
rs373768488 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096538 | TCACATAAGTGAAAT[C/T]GTGCTGTATTTGTAC | 6045 |
rs373783964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185093492 | TTCTCAACTTATTCT[A/G]TTTCTTCTCTTTATA | 6045 |
rs373851059 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060918 | GAGGCCAGGAGTTCA[A/G]TACCAGCCTGGGCAA | 6045 |
rs373983014 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068863 | CTCACTCATATTAAA[C/T]TATAGCTTTATTTCA | 6045 |
rs374010603 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076758 | TGTTTTGTTATATTG[A/T]TCTGTTTTTCTTTTT | 6045 |
rs374109131 | snp | C/T | 1.80693e-05 | 0.00300571 | intron-variant | RNF2 | GRCh38.p7 | 1:185099757 | CTCATTGGCATATTC[C/T]AGAAATGAAATTTTT | 6045 |
rs374254619 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | RNF2 | GRCh38.p7 | 1:185096199 | TCTTTATGTTGTGCT[A/G]TCAATTTTTTGTCCC | 6045 |
rs374261242 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047089 | GCAAAATAATAGGTA[C/G]TTATAGGTGACTCCT | 6045 |
rs374264610 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092894 | CCAAAATCTTGCTTA[C/G]CCACTAGTCAGATTT | 6045 |
rs374294193 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048751 | GTCGATGCATAGAAT[C/G]AAAATCACATGTAGT | 6045 |
rs374335504 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089048 | GTGTTTCCATGGATT[A/G]GAGGTGGGTGGGTGG | 6045 |