SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs374364046 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075245 | GTGATCCCCCCGCCT[C/T]GGCCTCCCAAAGTGC | 6045 |
rs374376539 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052332 | CAAATGTCTGTCAAC[A/C]GATGAATGGATAAAC | 6045 |
rs374476570 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069686 | ATCTTAATCCTCTCA[A/G]AGATTGGGTATGTGT | 6045 |
rs374535469 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052737 | CCATCGTTTTAGGTG[A/C]GCTGAAAAGTTTGAA | 6045 |
rs374576853 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057445 | GTGGTTCGTTTATAA[G/T]TTTTTTTTAAGATTT | 6045 |
rs374652984 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070794 | CAGGTGCCCGCCACC[A/T]CGCCGGCTCATTTTT | 6045 |
rs374785760 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076471 | AATTTTTTGTATTTT[-/T]AGTAGAGACGGGATT | 6045 |
rs374808904 | snp | A/G | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102619 | CCCCTAGCAACCTCT[A/G]TTCTACTTTCTCTTT | 6045 |
rs374875148 | snp | C/G/T | 0.000116525 | 0.00763224 | intron-variant | RNF2 | GRCh38.p7 | 1:185099984 | ATTTAAAATAATAGA[C/G/T]TGTTGAAACTGGGAG | 6045 |
rs374887478 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066500 | TGATTTCTGCTCTCC[C/T]ATTTGACTGCTTATT | 6045 |
rs374923302 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045239 | CAGAAGGTTGAGCAC[C/G]AGGTGGCTGCGCCGT | 6045 |
rs374953334 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090522 | TGAAATCTAACAAAC[A/G]TTTTATTAATGCTTG | 6045 |
rs374963714 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084599 | ACAAAAGGCCATTGC[A/G]TATTTGGTACTTTTT | 6045 |
rs374970424 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065578 | CAACTCCAGACGCGC[A/C]ACCTTTAAGAGCTGT | 6045 |
rs375045541 | in-del | -/CT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065859 | GGATGCTTTTTATTT[-/CT]GTTTCCTTTTTTTCC | 6045 |
rs375103044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069751 | TTTATAAATAATTTG[C/T]TAATTTCTAATGAAA | 6045 |
rs375155697 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044592 | CACACATTGGAGGCT[A/G]TGAACCTAGTTTGCC | 6045 |
rs375161113 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070879 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 6045 |
rs375174080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185057982 | ATACAAAAATTAGCC[A/G]GGCTTGGTGGTGCAC | 6045 |
rs375177268 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096560 | TATTTGTACTTTTGG[A/G]GTTTTTTTTTTGTTG | 6045 |
rs375317224 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064114 | AGACTTAATTCAGAA[A/G]GGCATTTAAAATTAA | 6045 |
rs375317772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078736 | CCAACATGGTGAAAC[A/C]CCATCTCTACTAAAA | 6045 |
rs375527799 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185096960 | AAGGCATTCTTTCAT[A/T]TTTCTTTTTCATTAT | 6045 |
rs375603292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185061011 | AGTCCTAGCTGCTTG[C/G]GAGGCTGACATGGGA | 6045 |
rs375653970 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054800 | CCTGCCGGGGTCAAG[C/T]GATCTTGCCACCTCA | 6045 |
rs375781471 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053924 | TAGATGTAGCTCATT[C/G]TTGGATGGATGTTAG | 6045 |
rs375803933 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090890 | TGCATTTTGGAGAGA[A/G]ACATCTTTAGGCATG | 6045 |
rs375886031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089167 | ATGTGCAGTTCTCAA[C/T]AGGGTTCGGACTCTT | 6045 |
rs376030738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071192 | GTAGAGGAAAAAGTC[A/G]GTTACGCATTCATCT | 6045 |
rs376053019 | snp | A/G | 3.35897e-05 | 0.00409802 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100316 | AGCCTTTAAAAACCA[A/G]TTCTGAGACTGAACT | 6045 |
rs376200603 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045225 | CAGAAGAACCCAAGC[A/T]GAAGGTTGAGCACGA | 6045 |
rs376235387 | snp | C/G/T | 4.95007e-05 | 0.00497477 | intron-variant | RNF2 | GRCh38.p7 | 1:185087678 | AGGGGCATATGAGAC[C/G/T]TGTAAACTGGGATAC | 6045 |
rs376237385 | snp | C/G/T | 3.32741e-05 | 0.00407875 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100305 | GAGCACAAATGAGCC[C/G/T]TTAAAAACCAATTCT | 6045 |
rs376397135 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050433 | GACTGCTATGTTCAA[C/G]CCAACTCCTGTGAAA | 6045 |
rs376435309 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059731 | TGAGACCATTAAGCA[C/T]GTTAATAGCATTATT | 6045 |
rs376522598 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081424 | TTGAGGTGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 6045 |
rs376535231 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052212 | GCACTCTTGACCTCT[C/T]CTACCACTAAACCGG | 6045 |
rs376540817 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053383 | CTATGTTGCCCAGGC[G/T]GGAGTGCAGTGAGGC | 6045 |
rs376600496 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044686 | TGGTTATCTTCTCAA[C/G]AGAACATGACATCTC | 6045 |
rs376757799 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058988 | TTAGATTTATCAGAG[C/T]TATAAAACTTCTACT | 6045 |
rs376790892 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087028 | GCTTTTACTGTCAAG[C/T]AGTTCATATTTATAA | 6045 |
rs376791167 | snp | C/T | 6.64849e-05 | 0.00576524 | intron-variant | RNF2 | GRCh38.p7 | 1:185091783 | TACTTAATTGTACCA[C/T]GAAAGTGCTTTCCAG | 6045 |
rs376878509 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057536 | AGTACCTGTTGTCCC[C/T]GTAAGTTTACCTTTC | 6045 |
rs376989599 | in-del | G/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057511 | TGTGGCGGTGGGATG[G/TT]AAGTAAAGCAGTACC | 6045 |
rs377031718 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066405 | CCTTCAGGACTGCTT[G/T]CTTTCCTCGCTTGGT | 6045 |
rs377067291 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185086368 | AGAGTGAGTTTTTTT[A/T]ATCTACAACCCTCTT | 6045 |
rs377185215 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054440 | GCACGTCTGGTGATA[C/G]CTGGGCCTTGCAATA | 6045 |
rs377222723 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185089112 | CTCAGATCATCAGGC[A/G]TTAGATTATAATAAG | 6045 |
rs377241883 | snp | A/G | 3.32447e-05 | 0.00407691 | intron-variant | RNF2 | GRCh38.p7 | 1:185099981 | AGTATTTAAAATAAT[A/G]GACTGTTGAAACTGG | 6045 |
rs377297650 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087136 | AACAATTCCTAAAAA[C/T]CAGTTTTGAGATTTA | 6045 |
rs377431183 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082637 | TGGGGTTACAGGCGT[C/G]AGCCACCGCACCCAG | 6045 |
rs377503318 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061441 | ACCAAACAAAAAAAA[A/C]CACACAAGATCACAA | 6045 |
rs377605835 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092421 | ACCTCGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 6045 |
rs377635622 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047389 | TTTTCTCTGCCTGTG[A/T]GAAGCTCCCAGGTTT | 6045 |
rs377635787 | snp | A/G | 1.64806e-05 | 0.00287054 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098093 | GCGAGGCAAGAAACA[A/G]CAGATTGAAAATGGT | 6045 |
rs386368980 | in-del | -/TTTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082363 | TTTTTTTTTTTTTTT[-/TTTTT]TTTTGAAGACAGAGT | 6045 |
rs386368981 | in-del | -/TTT | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101852 | TTTTTTTTTTTTTTT[-/TTT]TTGTAATCTGTGCCA | 6045 |
rs397950861 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185100185 | CATAATTTTTTCTTT[-/T]CTTTTTTGTTTTAGG | 6045 |
rs397959311 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065969 | CATTTTTTTTTTTTT[-/T]AGTATCAGCATCTAC | 6045 |
rs397982247 | in-del | -/G | 0 | 0 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045377 | AGGCCCGCGGCGCGA[-/G]GGGAGGGTGCGCCGC | 6045 |
rs397982248 | in-del | -/A | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185051746 | AAATTCTGAAAGATG[-/A]AAAAAAAAAAAGAAT | 6045 |
rs397982249 | in-del | -/A | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185068020 | CAAGACTCTGTCTCT[-/A]AAAAAAAAAAAGGCC | 6045 |
rs397982250 | in-del | -/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185088569 | AATACTTCCTTTAGC[-/T]TTTTTTTTTTTTTGA | 6045 |
rs398049853 | in-del | -/T | 0.5 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185061145 | TTTTTTTTTTTTTTT[-/T]GAGACGGAATCTCGC | 6045 |
rs398074482 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088568 | CTCAAAAAAAAAAAA[-/A]AGCTAAAGGAAGTAT | 6045 |
rs527277377 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070375 | TTACTGTGCTTTCTG[A/G]CTGTCTCATTTGTTG | 6045 |
rs527279250 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074627 | AAAAAGACCAGATAC[A/T]GTCTGCCTTCCTGTA | 6045 |
rs527338452 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185058595 | TCCTCTTTATTGTTC[A/G]GTAATGTGGAATGAG | 6045 |
rs527418411 | snp | G/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044343 | TCCAAGGCGTCAAAG[G/T]CCATCTTAAATCCCG | 6045 |
rs527423745 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185074719 | CTGAACGTGTACAGA[-/T]TTTTTTTCTCGTGTC | 6045 |
rs527476214 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185076585 | GCCACTGCGCCCGGC[C/T]TTATTTTATGGTTTT | 6045 |
rs527549151 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185077720 | GTTTTGTTTTGTTTT[G/T]TTTTTTTGGGCTGTT | 6045 |
rs527550932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071349 | ATATGTATCCTGAAA[C/G]ATTAAGACGAGGGAA | 6045 |
rs527590770 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099145 | CAACCTTTGCCTCCC[A/G]AGTTCAAGCGATTCT | 6045 |
rs527678064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085746 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC | 6045 |
rs527755593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072830 | CTGTAGTCCCAGCTA[C/T]TTGGGAGTCTGAGGC | 6045 |
rs527792833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079286 | GGGCCTGTGAAACAA[A/C]ATTTTTGGGAGGCTG | 6045 |
rs527876122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099658 | AGCAGTAAATTTCTG[A/G]TATTATTTTGTCAAT | 6045 |
rs527908197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059246 | AAAAAAAAAACCTCC[A/G]TAATAGTTTTTCTTT | 6045 |
rs527908224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052147 | TTCAGACCATTTCAG[A/G]CTCATTCCTTCCTCC | 6045 |
rs527949582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085324 | CAGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG | 6045 |
rs527985493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092164 | TTTCTCCTTTTTCTT[C/T]TTTCCCCTTTCCCCT | 6045 |
rs528025090 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043921 | GCTTCCCAGGTTCAA[G/T]CGATTCTCCTGCCTC | 6045 |
rs528117471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185087868 | GGTGAATAAAACAGA[C/T]GTAGCACCAACCATG | 6045 |
rs528147407 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069315 | CACAAAAACCAACTT[C/G]GCATGGTGGTTCATG | 6045 |
rs528184224 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089373 | TATGCAAACATCATG[C/G]CATTTTTTTATAAGG | 6045 |
rs528197377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081767 | GCATTGTTGTGGATA[A/G]GAATTGGGCCCTTTT | 6045 |
rs528203702 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185075023 | ATTTTTGAGATGGAG[C/T]CTTGCTCTGTCGCCC | 6045 |
rs528312110 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102694 | CACATTATTTTCAAG[G/T]TTCATGTGATAGCAT | 6045 |
rs528319197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054845 | TGGGACCACAGGCGG[A/G]CGCCGCCACGCCCGG | 6045 |
rs528382354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048163 | GGTCATGGGACTCTT[C/G]GCATTTAAGTAGAAG | 6045 |
rs528395246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087241 | TTACAGTTCTGGAGA[C/T]TGGGAATTCCAAGAT | 6045 |
rs528405212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095627 | ACACCATTATTTAGA[A/G]CCATGCTTGGCTTAA | 6045 |
rs528408514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185047137 | AGCAAATATGGTCCC[C/T]CACTTTTTGTAAGGA | 6045 |
rs528517661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096473 | CCTCCCCCCAGTTCC[C/T]GGTAACTGTCATTCT | 6045 |
rs528593421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097554 | GAAAATTATTTTTAA[A/G]AGATAGCGTCTTACT | 6045 |
rs528594369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185049996 | ATCCCAGCTGGCAAA[G/T]GAGTTGATGAAATAT | 6045 |
rs528679598 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093779 | TTGTATGTCATTAAC[C/T]GTTCCTTTACTTGTT | 6045 |
rs528717328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056419 | ACTGGAGTGCAGTGG[C/T]GTGATCATAGCTTAC | 6045 |
rs528741406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063892 | TGACTCTGCTTCTCA[A/C]ATCACATCGCTTTGT | 6045 |
rs528747420 | in-del | -/T/TTTTTTT/TTTTTTTTTTTTTTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077625 | TAGGAATTAACTTTG[-/T/TTTTTTT/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTGG | 6045 |
rs528826190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063318 | GATGAGGGGTAAAGA[C/T]ACTGATTCAGTGAGT | 6045 |
rs528839523 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100665 | CTGCTCCCCTCAAAA[G/T]ATTTTTAGTCATACA | 6045 |
rs528926894 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092160 | TTCCTTTCTCCTTTT[G/T]CTTCTTTCCCCTTTC | 6045 |
rs528977238 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045586 | GCGCCGGCGTCCGCG[A/G]CAGCTGATACCAGAG | 6045 |
rs529065146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072207 | GTTGAAGCAATAAAC[C/T]AAGGTGACTGTGAAG | 6045 |
rs529112304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185059500 | GATGCAAATTAGTGT[C/T]ATCTCTAATCACATT | 6045 |
rs529148224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066655 | AATGGTTGAACTCAA[C/T]TGGTTTTCATTATGG | 6045 |
rs529203661 | in-del | -/CGTGC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088425 | CCAGGCATGGTGGCA[-/CGTGC]CGTGCCTGTAGTTGC | 6045 |
rs529223052 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185060010 | CCATTGACACAAGGG[-/A]ATGTTACTGTGACTT | 6045 |
rs529226600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185058107 | TTCCAGCATTGCTGA[C/T]AGAGCGATACCCCAT | 6045 |
rs529271979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060208 | GTCTTTAATTCAGAT[A/C]TGTGTAAATCTTTTA | 6045 |
rs529436261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086326 | TATTAGGATGACTGG[A/G]GTCACTTCATTTTTC | 6045 |
rs529436755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068193 | AATTAAGGAAACAGC[A/G]TGTATGCAGGATAAA | 6045 |
rs529438156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079487 | ACCTTTTAAAGGAAA[A/G]CATCTTTGAAACAAC | 6045 |
rs529457383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060891 | TGGGAGGCTGAGGTA[C/G]GAAGATCACTTGAGG | 6045 |
rs529494033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046233 | GGGGAGACCCCTTCA[A/G]CTTCACACATTCCTG | 6045 |
rs529533818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073511 | GTGTATTCTCTTTCA[C/T]TGGCATCTATTTTTC | 6045 |
rs529669668 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086175 | CCCCAATCCACCTCT[A/G]TAATTCCATATATTT | 6045 |
rs529679941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070869 | TCTCGATTTCCTGAC[C/T]TCGTGATCCGCCCGC | 6045 |
rs529789359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071314 | ACAGAACTCAGTTTC[C/T]GGGCTAGTTTATAGG | 6045 |
rs529828644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081882 | TGGGATTCAGAAAAC[C/T]GTAGTGGATCAGAAA | 6045 |
rs529828860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089923 | GTAATCCCAGCTACT[C/T]GGGAGGCTTTTTTTT | 6045 |
rs529854383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049876 | TGCTAACTGCCAGGG[C/T]CAGGGGCTGCATTTG | 6045 |
rs529856233 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185099530 | GATTTTTGTCACTGT[G/T]TATCTCATTTTATAG | 6045 |
rs529867610 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077820 | CTAATGCCTGATTCA[G/T]TGTTTTTTTTCAGTC | 6045 |
rs529963586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076430 | CAAGTAGCTGGGACT[A/G]CAGGCGCGTGCCTCC | 6045 |
rs530025697 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185054598 | GGACCCCGAGGCCAC[A/G]CCTCTAGAGGCGGGG | 6045 |
rs530045403 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043895 | CGCGATCTCGGCTCA[C/T]TGCAACCTCTGCTTC | 6045 |
rs530047131 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185078913 | GCCAGGCATGGTGGT[A/G]TGCACCTGTAATCCC | 6045 |
rs530102385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078581 | GTGATGTACTTAGTG[A/G]TCTTTCATATGAATA | 6045 |
rs530108046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084273 | TAAACCATGCCTTAA[G/T]TCAGTTTATGTTGGC | 6045 |
rs530142997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091387 | GAGCATTTTTATAAC[A/C]GTGGTGGTGAGGCTG | 6045 |
rs530183668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185071909 | TCTGTCACTTTCTCA[C/T]TATATTTTCTCTCCT | 6045 |
rs530213434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077972 | AGTAAGGGGCCGGGC[A/G]TGGTGGCTCACGCCT | 6045 |
rs530218693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085305 | AGGCGCCCGCCACCG[G/T]GCCCAGCTAATTTTT | 6045 |
rs530318667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052044 | GTTTCAGTGTTAGCC[C/T]TCCCTGCCAATCCTC | 6045 |
rs530340974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098648 | CAAGAATGGCTACGT[C/T]ACCACTGTATCTCCA | 6045 |
rs530364946 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082993 | TTGCACTAACCTAAT[A/C]TCTACAAAGAAGCTG | 6045 |
rs530431162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090611 | TTGACCATATAAAGA[A/G]AGCACAAGTATGATG | 6045 |
rs530451694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051337 | AGAATTGAATGCAGG[A/G]GACTTGGTTTCTAGG | 6045 |
rs530486380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074371 | GGACTGTAGGGGTAG[G/T]ATGGGACTGAATGTT | 6045 |
rs530518204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087115 | GTTTTTTTTATTCTC[A/G]AGATTAACAATTCCT | 6045 |
rs530527801 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185046999 | TGGTTATTCCCTTTT[C/T]CCCCTGAAATTTCTA | 6045 |
rs530556531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095119 | TTTACCAAAGTATAA[C/T]GTACTAAATGTTAAA | 6045 |
rs530571895 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101897 | CACCAAAAATCAAGG[A/G]AACTTTTATATATTC | 6045 |
rs530602285 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185081148 | AAACACATCTTTATT[A/G]ATCAAAATAGGAACC | 6045 |
rs530679592 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054827 | CTCAGTTTCCTGAGT[A/G]GCTGGGACCACAGGC | 6045 |
rs530738410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060697 | ATCAGTAGACTGGAA[A/G]CCCTTTGGCAAGCAG | 6045 |
rs530767419 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057421 | CATAGTATATTTAAT[A/C]ATTTCATTGTGGTTC | 6045 |
rs530826025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055647 | CTCGAACTCGAACTC[C/T]TGATTTCAAGTGATC | 6045 |
rs530827114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063232 | TAATTTTTACACAGA[A/C]TACGTAGAATAGTGG | 6045 |
rs530855897 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102558 | TTCATCACCCCAAAC[A/G]GAAACTCTGTGTGCA | 6045 |
rs530856836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061278 | GACTACAGGCGCCCG[C/T]CACCATGCCCGGCTA | 6045 |
rs530956732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078054 | GGTTCGAGACTAGCC[C/T]GGCCAACATGGGTGA | 6045 |
rs531048268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096430 | AATTGAAACCCTGTA[C/T]CCATTAAGCACTAAC | 6045 |
rs531060266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056283 | TGGAATAATTGATTT[A/G]GGAAAATTAAGACAA | 6045 |
rs531145856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069228 | AAGGCCAAGGTTGGC[G/T]GATTGCTTAAGCCCA | 6045 |
rs531164515 | in-del | -/TAAAG | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185074819 | AATCTAGAGATGATT[-/TAAAG]TACACAGGAGGAGGG | 6045 |
rs531223609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065981 | TTTTAGTATCAGCAT[C/G]TACACAGCCACAAGC | 6045 |
rs531299506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053098 | ATTTGAACCTAGGCA[A/G]GTCAGGCTCTAGACA | 6045 |
rs531337654 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059404 | ACAGTAATAGTGGGA[C/G]TTGAAATACTGAGGG | 6045 |
rs531389422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077823 | ATGCCTGATTCATTG[G/T]TTTTTTTCAGTCATT | 6045 |
rs531414077 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | RNF2 | GRCh38.p7 | 1:185072952 | CTCAAAAAAACAAAC[-/A]AAAAAACATAGTGAA | 6045 |
rs531454987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072125 | CTTGGGGCTGCTAGA[A/G]GGTGCTGTGAGGAGG | 6045 |
rs531456781 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065238 | ACCAATCAGTGCTCT[G/T]TGTCTAGCTAAAGGA | 6045 |
rs531474381 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045609 | TACCAGAGTCTTGCT[C/G]CGGCCGCGGCCAGCG | 6045 |
rs531715320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072855 | TGAGGCAGGAGAATC[A/G]CTTGAACCCACGAGA | 6045 |
rs531716818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079885 | CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCTA | 6045 |
rs531821761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185092269 | GCAACCTCCACCTCC[C/T]GGGTTCAAGTGATTC | 6045 |
rs531882037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067084 | TAAGTGCTTTCTGTT[G/T]TATGTTCCATATTGT | 6045 |
rs531906817 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045290 | GCTACGTCGGACCGC[G/T]GTGGGCGCCGGGGGG | 6045 |
rs531933054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185085378 | CCTGACTTCATGATC[C/T]GCCTGCCTCGGCCTC | 6045 |
rs531944099 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044819 | TGGCTGTGTTTTAGG[C/T]AATGATTACATCTAT | 6045 |
rs531982905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069775 | AATGAAATTTAAGCC[C/T]GAAATATCTCTGTTC | 6045 |
rs532184682 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073617 | GTTTAAGGTACCTGT[A/G]TATGTTAAAATGCAT | 6045 |
rs532202492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087980 | TGTAATAAGTACTGA[C/T]AAGGCACCAAGGAAG | 6045 |
rs532206988 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095713 | TATATTGAATTAAAA[G/T]TAGTCTCTTGTGTGC | 6045 |
rs532238697 | in-del | -/GT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074982 | ACTATATATAGTTCC[-/GT]GTGTGTGTGTGTGTG | 6045 |
rs532289974 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185076351 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 6045 |
rs532346124 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185049337 | TGTGCTACATTAAAG[A/G]AGGTGAGTGTGTGTG | 6045 |
rs532369904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048377 | AGGCTTAGTTATGTA[A/T]CTTGTTGGATGCTCA | 6045 |
rs532375125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051235 | TCTTATTCAGTCTGG[A/G]ACGGCTGTCTTGGAA | 6045 |
rs532445915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088803 | ATGTGCTAATAAGTA[C/T]TATGTTGAATCCATG | 6045 |
rs532484276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185049055 | ACTTGGTGAAACTCC[A/G]TCTCTACTAAAAATA | 6045 |
rs532549987 | in-del | -/TTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091222 | AGACAATGTTAAATA[-/TTT]ATTATTTAGACTCAG | 6045 |
rs532588535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097640 | CTGGGCTCAAGCCAT[C/T]CTCCTGTCTCAGCCT | 6045 |
rs532610681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077298 | CCCATCCTCCTCCCC[A/C]CTCCCTCCTACTTCT | 6045 |
rs532648720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083294 | GTATTTTGTCAGTTT[C/T]CTCAGGTTCTTTGAA | 6045 |
rs532687223 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185057816 | AGGGGAAAAAAAAAA[A/C]AAACAGTAAAACAGT | 6045 |
rs532724246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185064467 | TTTCAACTTTACAGT[A/G]GTACAAAAGCAATAT | 6045 |
rs532786313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054330 | TTCAGAACTGTTCAC[A/G]TACATAACCGGCAAG | 6045 |
rs532823658 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098910 | GCTCATGCCACCAAG[C/G]CCAGCTAATTTTTGT | 6045 |
rs532834281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080112 | GTGGCACCTCACTTC[G/T]TATCTTCTTTGCTGG | 6045 |
rs532863009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046798 | TTTGCATTACATAAT[C/G]TACTTTTGGTAATTC | 6045 |
rs532880742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097102 | GAGGCAAATTATTTA[A/C]TCTTGTACCTGAGTT | 6045 |
rs532897152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092474 | GCCACCGTGCCTAGC[C/T]GAGAAATACATTTTC | 6045 |
rs532899689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046360 | TTCTGCGGGAAGATT[A/C]GCGTTTTGAACCGTG | 6045 |
rs532904553 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070112 | TAGGGGACTAGGAAA[C/T]AGAAATGCTTCTTCA | 6045 |
rs532951991 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094440 | TCCACCACACCTGGC[C/G]TTGGAGTCGCTTTTA | 6045 |
rs532964898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066762 | TCATATTAGACCTTG[A/G]TAGGTGTATCTTAAA | 6045 |
rs532991004 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067627 | TTTTCTTTGTTTCAT[A/T]GTGCTTAGGGAAGTG | 6045 |
rs533017357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053791 | AAAAGGAGTAGTGCA[C/T]GTGACATTAAGTAGT | 6045 |
rs533111606 | snp | C/T | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185063974 | GGATAATCTCCCCAT[C/T]TTAAGAGCTGTAATT | 6045 |
rs533122946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060096 | CAGGAAAGGATAACA[A/G]TCTTGGAATATACCA | 6045 |
rs533402501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068395 | TAAGTTAATGGTATT[A/G]AGATGAGATTGTCCT | 6045 |
rs533402825 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185074817 | GTAATCTAGAGATGA[C/T]TTAAAGTACACAGGA | 6045 |
rs533423178 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055982 | ATTGTAAAGTAATGT[A/G]TGTTTTTAAAGGCTC | 6045 |
rs533423337 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185055509 | CACTGCAGCCTCCGC[C/G]TCCCAGGTTCAAGCT | 6045 |
rs533465618 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061188 | GCTGGAGTGCAGTGG[C/T]GGGATCTCGGCTCAC | 6045 |
rs533473277 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091024 | TGGAAAAGAATTTTC[A/G]GGGTTCAAAAGTATT | 6045 |
rs533488182 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185074236 | GACCTTCCACGAGTT[C/T]CATCATTTAAAAATT | 6045 |
rs533510448 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185052412 | ATAAAGTACTGACAC[-/AT]GTTACAATGTGGATG | 6045 |
rs533814815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064020 | AGTCCATTTTGCCAT[C/G]TAAGGTTAACATGCA | 6045 |
rs533829512 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185051400 | TTCTGAGTCTCTTTT[C/T]TTTTGTTAAAAAAAA | 6045 |
rs533852432 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070883 | CCTCGTGATCCGCCC[G/T]CCTCGGCCTCCCAAA | 6045 |
rs533919927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050554 | TCTTTGCACTTTTAG[C/T]TTAGTACTGTGCACA | 6045 |
rs534051365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056895 | AAAAATGCTTTTGGT[A/T]CTTAATCAGTCTTAT | 6045 |
rs534076128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065485 | ACTACTACCTTTATG[A/G]GCTGTAACACTCACC | 6045 |
rs534101857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063636 | CAACACAAACTTACT[A/G]TTTTACAGTTCTGGC | 6045 |
rs534166092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185071935 | CTCCTCATGACATTG[A/G]TGAAGAAATGTCATG | 6045 |
rs534177616 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064841 | ATTTTATGTTGTTGT[A/G/T]TATGGAATTTTTTTT | 6045 |
rs534265538 | snp | A/C | | | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093268 | ACTGAAGATACAGGC[A/C]ATGAACAGGTATATG | 6045 |
rs534269227 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185066193 | AAAGGTGATCTCTTC[A/G]TCATTGCACTGTGGA | 6045 |
rs534313188 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083985 | CTCACTCTGTTGCCC[A/G]GGCTGGAGTGCAGTG | 6045 |
rs534317474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067913 | ATGGGGTTTCACCGT[C/G]TTGGCCAGGATGGTC | 6045 |
rs534353666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073886 | TCAGTTCAGTGGTTA[C/T]GCTACTCAGAGTGAG | 6045 |
rs534383673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061754 | AAAGACATTGCTAAA[A/G]GTAGAGTATTTTCTT | 6045 |
rs534632611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080868 | TGATAGTTCCTATTA[A/C]TTTTCCAGGGTAGCG | 6045 |
rs534691538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081502 | GGGTTCAAGTGATTA[G/T]CCTGCCTCAGCCTCC | 6045 |
rs534798421 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185075167 | CCTGGCTAATTTTTT[A/T]ATTTTTAGTAGAGAC | 6045 |
rs534856154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085941 | ATAGGGATGAGCCAC[C/T]GCACCTGGCCCTGTT | 6045 |
rs534892836 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185082475 | CCTGCCTCAGCCCCC[A/C/G]AGTAGCTGGGATTAC | 6045 |
rs534979645 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076674 | TTTATTTGAAAAGGG[-/T]TTAAATTTTTTTTTT | 6045 |
rs535038375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084678 | CCCACATTCTTCATA[A/G]TAGCTGAGGTAACTA | 6045 |
rs535148295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091848 | GAGACAGAGTTTCGC[G/T]TTTCTTGCCCAGGCT | 6045 |
rs535191452 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185078314 | ACATGTCTTTTGCCC[A/C]CAAATTAGTCTTACT | 6045 |
rs535244500 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RNF2 | GRCh38.p7 | 1:185064758 | TGTAATACCTTTCAG[A/G]ATGTTTTGTAATTTT | 6045 |
rs535258651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058115 | TTGCTGACAGAGCGA[C/T]ACCCCATCTCAGATA | 6045 |
rs535281437 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103032 | TCTGTAACACTTGTT[A/G]TTTTCTTTTCTTCTT | 6045 |
rs535287657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048567 | CCTTGGGTTAAATTT[C/T]CTAATGAGAGCATAC | 6045 |
rs535348732 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052419 | ACTGACACATGTTAC[A/C]ATGTGGATGAACCTT | 6045 |
rs535350169 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050854 | TAAAATTCTCTCCTA[C/T]TTCTTAGTATTTTAT | 6045 |
rs535367367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098985 | TCGATCTCTTGACCT[C/T]GTGATCCGCCTGCCT | 6045 |
rs535384932 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185092334 | GGCGTGTATCACCAC[A/G]CCTGGCTAATGTTTG | 6045 |
rs535434103 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058863 | GCTCATTTTATAGAT[A/G]AAGAGGTTTAGGTCT | 6045 |
rs535436230 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089803 | GGAAGGCCGAGGCCG[G/T]TGGATCACCTGAGGT | 6045 |
rs535444224 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062567 | TGCAAGAAAGTATAG[A/G]TGGTTGTTTTTTATA | 6045 |
rs535447445 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101195 | GAAAAGTACAAGATA[C/T]GTTCAAAGCTTCCCT | 6045 |
rs535536423 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185045997 | CGGCGCGGTCCCCTC[C/G]CCTCCGGGGGCGGGG | 6045 |
rs535569931 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044858 | TACTTCGTAAATCCT[C/G]AAGTTCAGAAGGTAA | 6045 |
rs535584487 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066523 | TGCTTATTTATGCCT[C/T]CTTAGCATTTATCAA | 6045 |
rs535618986 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185048572 | GGTTAAATTTTCTAA[-/T]GAGAGCATACTATTA | 6045 |
rs535646320 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079491 | TTTAAAGGAAAGCAT[C/G]TTTGAAACAACCAGT | 6045 |
rs535668752 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185072476 | GGTTAAGAAAAGAGA[A/G]AACGTGAGATAAAGA | 6045 |
rs535755130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185087418 | ACCTGATCACCTCCC[A/G]AAGTCCCCACCTCTT | 6045 |
rs535805688 | in-del | -/TC | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185065858 | TGGATGCTTTTTATT[-/TC]TGTTTCCTTTTTTTC | 6045 |
rs535913843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054470 | ACTGGCAAGCAGGCC[G/T]TCTTCTCCCATCTGG | 6045 |
rs535923297 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102156 | TCAGTATGGGAGGAT[A/G]TAAACTGCATCATTA | 6045 |
rs536003353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053963 | ATTGAATGTAGCAGC[A/G]TTCACTTAACCAGTT | 6045 |
rs536109203 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185084942 | ACAGGAATGAGGGAC[A/T]TGTTGTGTCTTCAGG | 6045 |
rs536120123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067130 | AAATTAGGAATTGAT[A/G]TTGCTTCTTTAAATA | 6045 |
rs536131098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070555 | GTTGAATGGGAACCT[C/T]AATTAGTATTATCCT | 6045 |
rs536142630 | in-del | -/TCTT | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185054672 | TCAGTTTCTTTTTAA[-/TCTT]TCTTTGTGGGTTTTT | 6045 |
rs536183793 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084612 | GCATATTTGGTACTT[C/T]TTTTCCTTTCCTTTC | 6045 |
rs536235673 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053026 | TATAGACAAGGAAAC[C/T]GAGGAATTAAGAAGT | 6045 |
rs536363195 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046035 | CCTCTCTGCAGCCCT[A/G]CTCCGGAGGCGGACG | 6045 |
rs536396745 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049715 | ATTACAGTAATCAGA[A/G]CCTAAGAGCTCAGAG | 6045 |
rs536445195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075138 | TAGCTGGATTACAGG[C/T]ACCCATCACCACACC | 6045 |
rs536648471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071125 | ATGGTTACATTCTTA[C/T]AAGGCTCTGGTTAGC | 6045 |
rs536671985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185083500 | TCCCCTCCACTCTTC[A/G]CTTTCTCTCTCCTTC | 6045 |
rs536722988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067851 | GAGTAGCTGGGACTA[C/T]AGGCGCCTGCCACCA | 6045 |
rs536796966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090029 | CAGATTCAAATGATT[C/G]TCCTGCTTCAGCCTC | 6045 |
rs536960742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082754 | GTCTCCACTGCTTTA[C/T]GAACCATTTTGAACT | 6045 |
rs536978326 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045694 | CGCGGAAGCAGCGGG[C/T]CGGGACACGCGTCTA | 6045 |
rs537000765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185087463 | GAGATTAGATTTCAA[C/T]GTAGGAATTTTGGTG | 6045 |
rs537060994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185081315 | AAAAAGTTGTCAAGA[C/T]GCTTGAAGAAGTGGT | 6045 |
rs537069839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086473 | ATATCGGGAAAGGAG[A/G]CAGAATTAATCAGCG | 6045 |
rs537098313 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185057065 | TGTAATCCAGTACTT[C/T]GGGAGGCAGAAGCAG | 6045 |
rs537158704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083163 | TTCTGCTTGCTTTAT[A/C]TACTAATATCTTACG | 6045 |
rs537162525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073808 | GACACTAAATATGTG[G/T]TTTTTTGCTACACTA | 6045 |
rs537163973 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185081007 | TTAGAAATTCCTCCT[G/T]AGTAGTTTTGGTTCT | 6045 |
rs537195932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093640 | GATCTCTTCATTGTG[C/T]CATCTAATGGCTGAT | 6045 |
rs537211191 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102301 | TGCTATTGGCCATCA[C/G]TACCAACCAGGGTTT | 6045 |
rs537216517 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053700 | CCCATTACTAGAAGG[C/T]AGGGATTTTAATTAC | 6045 |
rs537224451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068515 | CAGTGTGACCACAGA[A/G]GCAGATTGGAGTGAT | 6045 |
rs537263923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053847 | AATAAATAAGATTAT[A/G]TAATGTGCAGTGTTC | 6045 |
rs537281132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092566 | TCTTTGTATTGAAAT[C/T]GCTGATTTTTAGACA | 6045 |
rs537291386 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100981 | AAAATCTTAAGTTCT[A/G]TGAGAACTTGGTTCA | 6045 |
rs537356692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085862 | TCACCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 6045 |
rs537384377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054653 | TCAAGATTGACATGT[A/C]GCCTCAGTTTCTTTT | 6045 |
rs537387217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061516 | GGAAAACGATAGCTA[A/G]CTCATTGTTTCAAAT | 6045 |
rs537401586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090790 | TCACTGCCAGCTTGT[G/T]GAGAGGGTAGTGAAC | 6045 |
rs537435267 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076525 | TCTCCTGACCTTGTG[A/C]TCCACCTGCCTTGGC | 6045 |
rs537456764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051528 | AGTTTAAGGGGTGTA[C/T]GTGAAGAAAAAAGTG | 6045 |
rs537469688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047611 | TCATTTCTATACATT[A/G]GCAAAGAAGCATAAT | 6045 |
rs537572104 | snp | G/T | 1.66515e-05 | 0.00288539 | intron-variant | RNF2 | GRCh38.p7 | 1:185091790 | TTGTACCACGAAAGT[G/T]CTTTCCAGGGTTTGA | 6045 |
rs537627616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064206 | TTCTATATAGTAAGT[C/T]ATGATTAATGTTTAT | 6045 |
rs537643848 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068518 | TGTGACCACAGAGGC[A/G]GATTGGAGTGATATG | 6045 |
rs537725302 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102909 | TTACTGCATCATATG[A/C]TAATTCTATGTTTAA | 6045 |
rs537787999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064707 | ATTTTGTCTTCAAAT[A/C]CATGAACATGGGATG | 6045 |
rs537953304 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096351 | CTTTTAAACGATTGG[C/T]TCCTCAAAGCTGAAC | 6045 |
rs537976621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052295 | CACCGCTATTCATGA[C/T]ACCCAAAAAATGGAA | 6045 |
rs538402866 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185068467 | TATAAGAGAAGGGGC[-/AG]AGAGAGATTACAGCC | 6045 |
rs538479407 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045257 | GTGGCTGCGCCGTCA[A/T]CCGGGCGTTGCCCGG | 6045 |
rs538503622 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185065602 | GAGCTGTAACACTCA[C/T]TGCGAAGGTCCACAG | 6045 |
rs538541850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078764 | AAAATAGAAAAATTC[A/G]CCAGGCGTAGTGGCT | 6045 |
rs538565057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081346 | AGTTGGTTGGCGAGA[A/G]GTCCGATGACTATGG | 6045 |
rs538618353 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | RNF2 | GRCh38.p7 | 1:185069504 | TACACATTTGAGGCT[A/T]TTTATCTAAGGGCTG | 6045 |
rs538636034 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185075976 | AGCACAGTTTAATTT[G/T]ATTGGTTATGTATTG | 6045 |
rs538652912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185082644 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCTGCAG | 6045 |
rs538683783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055822 | TGTTGTTTAGTTTTA[C/T]GAACCTATCCTTTTG | 6045 |
rs538711118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070967 | TATTCCCTCAACTAA[C/T]TTAAGGATTGTATCT | 6045 |
rs538768005 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF2 | GRCh38.p7 | 1:185076622 | TATGTTAATCCTTCC[A/G]GAATTTTAAAATTCA | 6045 |
rs538824792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080892 | GGTAGCGTTCAGTAG[A/G]CAGAAGGAGTGTTCT | 6045 |
rs538860709 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185048695 | TTTCTTTTTGTTTCT[A/G]TGCTATAGAGTGGAG | 6045 |
rs538863021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087384 | CACTAATTTCATTCA[C/T]GAGGGTGGAGCCCTC | 6045 |
rs538877446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056554 | ATTTTTTATTTTTGT[A/G]GAGACGGGGTTTAGC | 6045 |
rs538899688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068852 | ATAATTTATAGCTCA[C/G]TCATATTAAACTATA | 6045 |
rs538901558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075078 | CAGCTCACTGCAACC[C/T]ACACCTTCCGGGTTC | 6045 |
rs539060821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185082003 | CTTCAGTCCAACCAC[C/T]GAGCGGGTCGTCACT | 6045 |
rs539068929 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045611 | CCAGAGTCTTGCTCC[A/G]GCCGCGGCCAGCGGA | 6045 |
rs539072292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089991 | CAGTGGCGTGATCGC[C/G]GCTCACTGCAACCTC | 6045 |
rs539113083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073092 | CTTAATGTGTGTTGT[A/G]TACATATATTGAGTT | 6045 |
rs539196733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096554 | GTGCTGTATTTGTAC[C/T]TTTGGGGTTTTTTTT | 6045 |
rs539358109 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092385 | TTTCACTGTGTTGGT[C/T]AGGCTGGTCTTGAAC | 6045 |
rs539376671 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044342 | ATCCAAGGCGTCAAA[A/G]GCCATCTTAAATCCC | 6045 |
rs539395670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053229 | AAATCCCCTTCATAG[G/T]CTCCCCACATTCCAT | 6045 |
rs539409730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094860 | TATTTTCCATAGAAG[G/T]AGATAATAGTAAAGT | 6045 |
rs539410513 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101512 | AGAAAGCTTTGTTGA[C/T]AGATCAGAAATAAGA | 6045 |
rs539437133 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065350 | GGGCCAAATAAGGGA[A/C]TAAAAGCTGGCCACC | 6045 |
rs539450826 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185093563 | TATTCTTTTATGAAC[A/C]CCCTCCAATCAGACA | 6045 |
rs539497835 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102252 | GTATTTTGTGTGTGT[A/G]TGGATGTGTGTTTTG | 6045 |
rs539572819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086688 | TGAATAGGTAGCAGT[C/T]TGGGTCTCAACATTA | 6045 |
rs539580334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091952 | TCCAGAGTAGCTGGG[A/T]TTACAGGCATTGCCA | 6045 |
rs539639674 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055975 | TCAAATAATTGTAAA[A/G]TAATGTATGTTTTTA | 6045 |
rs539641894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085757 | CTCCCGGGTTCAAGC[A/G]ATTCTCCTACCTCAT | 6045 |
rs539693301 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099111 | GGCTGGAGTACAGTG[C/G/T]CACAATCTTGGCTGA | 6045 |
rs539778792 | in-del | -/CTTT | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185051383 | AGCAAGATTCTTGGC[-/CTTT]CTGAGTCTCTTTTCT | 6045 |
rs539803498 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043559 | TTCATCCATAAAGTT[C/T]CTGCGCTTTCTACAA | 6045 |
rs539858748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054532 | GGCTCTTCTCCATTA[C/G]GAGCGCTCTTCCTGA | 6045 |
rs539892833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096680 | TAAATGACCTCAGCA[A/T]GTCTATTCATGTTGT | 6045 |
rs539967538 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185054863 | CCGCCACGCCCGGCT[A/T]TTTTTTTTCTATTTT | 6045 |
rs540032894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062901 | ACAACAAAGAAGTAT[A/C]ATTTCCCTCCCACTT | 6045 |
rs540044266 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063219 | GTCACTGAAACAGTA[A/G]TTTTTACACAGAATA | 6045 |
rs540168949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067827 | ACGATTCTCCTACCT[C/G]AGCCTCTCGAGTAGC | 6045 |
rs540194790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081777 | GGATAAGAATTGGGC[C/T]CTTTTTGTTGATCAG | 6045 |
rs540218147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185049746 | AAGAGGTTCTATGGA[C/T]CCGGTGCTGGACTTT | 6045 |
rs540292184 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088131 | GATTTTTATATTAGT[A/C]TGAACTAAATACAAA | 6045 |
rs540407782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185055466 | CACTTTGCTCCTCAG[A/G]CTGGAGTGCAGTGGT | 6045 |
rs540508023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096279 | ATATAACAGAATTTT[C/T]CATCTTAACCATTTG | 6045 |
rs540573753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071190 | GAGTAGAGGAAAAAG[C/T]CAGTTACGCATTCAT | 6045 |
rs540574584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056010 | CTCTCAAATATTAAA[A/G]TACTATCTAGAATAG | 6045 |
rs540606624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097562 | TTTTTAAGAGATAGC[A/G]TCTTACTCTGGCCCA | 6045 |
rs540695838 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056144 | TCTGAAATATTTTTT[G/T]CAGGAGTTCTCCATT | 6045 |
rs540696571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054686 | ATCTTTCTTTGTGGG[C/T]TTTTTAAAATTTTTT | 6045 |
rs540709507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090403 | TTGATTACTCTCTGG[G/T]TCATCAATATACTCT | 6045 |
rs540713233 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085634 | TTTTGTGAACGATTT[G/T]ATCATGTCACTCTCC | 6045 |
rs540730236 | in-del | -/TCAT | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070209 | CTTCATATGAATATC[-/TCAT]TCAGTTTTGCTAGTG | 6045 |
rs540751946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094278 | GTCTTGAGTAGCTGG[G/T]AGTACAGGTGCACGC | 6045 |
rs540824724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076807 | CTTTCTATTAAGCTT[C/T]AATGTTTGTTTTAAG | 6045 |
rs540862133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185072712 | TTGGGAGGCTGAGGC[A/G]GGCGGATCATGAGGT | 6045 |
rs540863180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076147 | TTGCTCATGGTGTCT[C/G]TAGTTGATTTTGTAT | 6045 |
rs540864568 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094864 | TTCCATAGAAGGAGA[A/T]AATAGTAAAGTCCAT | 6045 |
rs540906963 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077715 | ATCTGTTTTGTTTTG[-/T]TTTTTTTTTTTTGGG | 6045 |
rs540933842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077451 | TTGTTTTGGGACTTC[C/T]GGTAGATTTTTCATG | 6045 |
rs541010819 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054500 | GGTCTCTGGCCCCTC[C/T]GGGCCGGCCAGACGC | 6045 |
rs541056829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185074113 | GTTATAAAGGACATT[A/G]TAAAAGATACAGCAT | 6045 |
rs541059146 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185081038 | CTGAAAGATCTATCT[A/C]GGATATATGTTAGAA | 6045 |
rs541110494 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102352 | ATTTCTTTTATCACT[A/G]TCTCAACTGAGGAAG | 6045 |
rs541134157 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069711 | ATGTGTTTGGAGCTA[C/G]GGAGGAGGGTAATCC | 6045 |
rs541467904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084008 | GTGCAGTGGCACAGT[C/T]GTACCTCACTGAAAC | 6045 |
rs541482416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062302 | ACAGTGTAGGAAGTT[A/G]TAGTGTATTAAGCTC | 6045 |
rs541521398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185069092 | CTAAAATTTTACAAC[A/G]TAGTGTAAGCTCTTT | 6045 |
rs541572730 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086926 | GGGTTAAGACAATCT[G/T]GTATACATTCAGCAG | 6045 |
rs541599037 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073659 | GTTCTAAGGGCTGAT[A/G]TGTCTACTGTTACTT | 6045 |
rs541599179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185046726 | TCAATTAAAAAAATT[A/G]AGGCATGGTTTCAGT | 6045 |
rs541624779 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043706 | TGAACTACACATGCA[C/G]TCGTCATGAAGGAAG | 6045 |
rs541646978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050819 | AGCAATTTTGACAGG[C/T]ATTCCTTTTGATGGC | 6045 |
rs541663342 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185097527 | AATTCTTATAGTCTT[C/T]TGTTTAATAAAGAAA | 6045 |
rs541701700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083105 | GCCATTGTTTTTTTC[C/T]CCTGCTTCTTTGTTT | 6045 |
rs541719283 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046908 | TAATAACTGAGGTGG[C/G]TGTGAGAGTTTGCTT | 6045 |
rs541725896 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054638 | CTAAATAATTGTCTT[C/T]CAAGATTGACATGTC | 6045 |
rs541905500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185092128 | GTCACTGCACCTGGC[C/T]GAGAAATACATTTCC | 6045 |
rs542086562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090922 | CAGTTAGATATAGCA[A/G]TACATTTTATACTTT | 6045 |
rs542113267 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056688 | TCATTCATTTCTTAA[A/G]TGGATTGTTTTTATT | 6045 |
rs542128305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185052799 | TGAAGTGCTGGGCAA[A/G]TATCAGCTGGGGATG | 6045 |
rs542141466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185099469 | TCATTAGGGTTTGGG[A/G]GGTATGTTCCTTTTT | 6045 |
rs542227148 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096215 | TCAATTTTTTGTCCC[A/T]TTATTTTAGCCCGTT | 6045 |
rs542243643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055983 | TTGTAAAGTAATGTA[G/T]GTTTTTAAAGGCTCT | 6045 |
rs542249531 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185066626 | TCACATGATAGCTCA[A/G]TAAATGTTTCCTAAA | 6045 |
rs542283477 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074620 | AAGAAAAAAAAAGAC[C/T]AGATACAGTCTGCCT | 6045 |
rs542320032 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077060 | GATTTTATAAATTTT[A/C/G]TTGCTATCGTGAATG | 6045 |
rs542359348 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045145 | GACGAACTCATGAGA[A/C]AGAAGTCTGAGCCCA | 6045 |
rs542403161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185048855 | TGTTGGAACACATTG[C/T]AGTTTCTTGGTGTTT | 6045 |
rs542404695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065741 | CACTGTGAAGTTCTG[C/T]GGCTTCGTTCTTGAA | 6045 |
rs542443229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072040 | TGGCAGTTGATGGTC[A/G]TGGTGGTAGGGGTTG | 6045 |
rs542473164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185065076 | CTTTTCTGTCTAGCT[A/G]AAGGATTGTAAGATG | 6045 |
rs542566282 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054545 | TACGAGCGCTCTTCC[G/T]GAGAGCGGGTTCCTC | 6045 |
rs542585312 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185072146 | TGTGAGGAGGTAGCA[-/G]GGGGCTGACTCTGAG | 6045 |
rs542611575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095533 | ATAGCACGTATCACT[C/G]TCTCATGTGTTACCT | 6045 |
rs542612631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087765 | AGCATTCCTGACTTC[C/T]GTATGTTGGCTAACA | 6045 |
rs542638026 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043438 | TCATATTAAGGATGT[C/T]AGCCTGAGGTCTAGC | 6045 |
rs542719293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057036 | AACCTGGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 6045 |
rs542722861 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185088544 | CTGGGCGACAAGAAC[A/G]AAACTCCGTCTCAAA | 6045 |
rs542808118 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065957 | GCTATACTGTCTCAT[-/T]TTTTTTTTTTTTAGT | 6045 |
rs542843317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061289 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 6045 |
rs542881216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055386 | TATCGTTTATTTTGG[C/T]TAGAAATTACTGTTG | 6045 |
rs542899576 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079445 | GTCAGCCTGAGTCTT[C/T]GTAATAAGGAAGTCC | 6045 |
rs542955699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062161 | GCAGGTAGCTTTGTG[A/G]CAGTTGTGTTGCTTT | 6045 |
rs542967616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185076007 | TGTTAATTACTCATC[A/G]TTTTGCTTATATTGT | 6045 |
rs543083408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049878 | CTAACTGCCAGGGTC[A/G]GGGGCTGCATTTGCT | 6045 |
rs543087087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060478 | CACTTAAGGACTCAA[A/C]ATTTTTCTGTTCTGC | 6045 |
rs543121272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185079704 | GGAGGCTGAGGTGGG[C/T]GGATCATCTGAGGTC | 6045 |
rs543123603 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185053682 | TGCATTTTCTTTTGC[G/T]CTCCCATTACTAGAA | 6045 |
rs543125802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067373 | CACAATTTATTATTT[A/G]CCTAGTCTTGAGTAA | 6045 |
rs543144581 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100525 | TTCCTTTAAAAAAAT[A/G]TATCTGAAGTTTCTT | 6045 |
rs543164893 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185075497 | AGTGTTCTTGCATTG[C/T]TGTGTAACTCCCTGA | 6045 |
rs543198011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082061 | GCAAGTTGCAATCCA[A/G]TGGTTCATTGTTGTT | 6045 |
rs543469308 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185087726 | ACTTAAATAGAACAT[A/G]GAGTAATAATAAATT | 6045 |
rs543494201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185079887 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCTAGC | 6045 |
rs543503258 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185072061 | GTAGGGGTTGCTGTC[A/C]TCATGGGAGGTGGCT | 6045 |
rs543577226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094141 | AGTCAGTTTTTTTTT[A/T]TTATTTTTTTTATTT | 6045 |
rs543713842 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185079051 | TTGGAGCTGCCAGCT[C/T]TCACGGTCTACTATG | 6045 |
rs543812421 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185082971 | CAGTGCAAAAACCAC[A/C]ATTAATTTGCACTAA | 6045 |
rs543844528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090183 | CCTCGGCCTCCCGAA[A/G]TGCTGGAATTACAGG | 6045 |
rs543968485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096898 | ACCATTGGACTGTTA[C/T]TTCTTTGTTCTGGCA | 6045 |
rs544014897 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069951 | TCAGCCATTGATTTT[C/T]TGCTTATGAGGCACA | 6045 |
rs544019431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097936 | AACATGTGGGAAACA[A/G]TATCATCCAACTCAG | 6045 |
rs544078075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097398 | TAAGAATTTCTTTAA[A/G]GAGGCATAAATATCT | 6045 |
rs544079900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089802 | TGGAAGGCCGAGGCC[A/G]GTGGATCACCTGAGG | 6045 |
rs544258753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051995 | ATGTAACACTTCTCA[A/G]ATTAAGAAGTGGAAC | 6045 |
rs544543460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058352 | AACCCCATGGATACT[C/G]AGGGAGGACTGTACT | 6045 |
rs544551229 | in-del | -/GGG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088693 | GCCCTCCACATACAT[-/GGG]GTTCTGCATCTGTGG | 6045 |
rs544560687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049758 | GGACCCGGTGCTGGA[C/T]TTTTGAGTAGGTCAG | 6045 |
rs544572600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059043 | TCCTCTTCCTGGTCC[C/G]TGGCTTTCTTTCAGC | 6045 |
rs544581401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091325 | GACTAATTTCCCACT[A/G]GTAAGCTTTTAAATA | 6045 |
rs544618199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098610 | GATACTAGAGTACCA[A/G]TAGGCTCTAAAACTC | 6045 |
rs544655311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047963 | TTTAATACTGAGTAG[A/G]TGCCCATATAATTTG | 6045 |
rs544655696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062065 | CTCCACCTTGTAGCA[G/T]CAAATATTTTACAAG | 6045 |
rs544761423 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055226 | GATTTTCTAATATCT[A/G]CATTATACTTACCAG | 6045 |
rs544808203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071604 | GTTAAAGAGTTACTC[A/T]GCCATGCTAGATTCA | 6045 |
rs544986336 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095034 | GAGTGTAGTCAAGAT[A/C]AAAAACCACTGGCTT | 6045 |
rs544986586 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103095 | GATAGCTGTCTTACT[A/G]GATGTCTCCTTTCAT | 6045 |
rs545024324 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102527 | AATGATCACCGCTGT[C/G]TACTTGTAAAACTTT | 6045 |
rs545110174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095504 | CCTTACCCTCCCTGC[C/G]TCATTTTTTTCCCAT | 6045 |
rs545135078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063652 | TTTTACAGTTCTGGC[A/T]GTAAGAAGTCCAAAA | 6045 |
rs545252211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185061276 | GGGACTACAGGCGCC[C/T]GCCACCATGCCCGGC | 6045 |
rs545308228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074852 | GGTATGTGTAAGTTA[C/T]ATGCAAATGCTGTGT | 6045 |
rs545384117 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185072065 | GGGTTGCTGTCATCA[G/T]GGGAGGTGGCTAAGA | 6045 |
rs545402106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081529 | CTCCTGAGTAGCTGG[C/G]ATTACAGGTGTGTGC | 6045 |
rs545423783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071685 | TTTGATAGATTTCAC[C/T]TGCTCATTCAGGTAA | 6045 |
rs545424719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094487 | CCTGTATTCCAGTCC[A/G]TAAATAAACAAATAT | 6045 |
rs545429518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078437 | GCTTTCTTTCCTTCT[C/G]TAATATGTCTATTTT | 6045 |
rs545448991 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185056174 | TACTTGAAGAGTTCT[C/G]CATTACTTGGAAAGA | 6045 |
rs545493754 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054062 | CTTCACAAATGACTT[C/T]TGTATATGTGTACTT | 6045 |
rs545496691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072518 | AGAATTTCTTTAGAA[G/T]GCATGAGGGAGCTAG | 6045 |
rs545544801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081068 | AATAATGGCACATGT[A/G]TTAGTTTGGTACAAA | 6045 |
rs545548930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059281 | TTTTCTGCAAAAGAA[A/G]ATCTACCTATGTGAC | 6045 |
rs545644574 | snp | A/C | | | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091618 | ATTGTGGTTTCACCT[A/C]GAAGTCTACACAGTG | 6045 |
rs545665893 | snp | A/G | | | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087578 | GCTGTGCAGACAAAC[A/G]GAACTCAACCATTAA | 6045 |
rs545694198 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043663 | TAGAGCAAAAGTTCT[A/G]AATTATGAACACCTG | 6045 |
rs545729074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185091057 | AAAATGAAATTCTAT[C/T]AAGCTGTTTATAAAC | 6045 |
rs545757089 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046811 | ATCTACTTTTGGTAA[A/T]TCCAAGATGATCAGC | 6045 |
rs545927231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085756 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTACCTCA | 6045 |
rs545959558 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100381 | ACTGGCATTACTTTT[A/G]TGGACAGATCTTGGA | 6045 |
rs545996536 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099671 | TGATATTATTTTGTC[A/C]ATAATTGAGACATTG | 6045 |
rs546073761 | snp | C/G/T | 1.97943e-05 | 0.00314591 | intron-variant | RNF2 | GRCh38.p7 | 1:185093315 | AGGGTAGCTGTTTTT[C/G/T]TGAATACTTTATTAA | 6045 |
rs546086372 | in-del | -/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043987 | CGACACCTGGCTAAC[-/T]TTTTTTTTGTATTTT | 6045 |
rs546140998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086133 | GTTTATTTCATCTCT[A/G]CCAAAGCCTCCTTAA | 6045 |
rs546233312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046062 | GACGGAGTGGAATGC[A/G]AGTTTTTTCTCTGGG | 6045 |
rs546301798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185079782 | AAAAGTACAAAAATT[A/G]GCCAGGTGTGGTGCT | 6045 |
rs546515513 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092631 | CAACGCATAAAACCA[C/T]GATTTTTCCACTTAA | 6045 |
rs546541559 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050741 | GTAAATTTAAACTGC[A/G]TAGTACCAATAGGTG | 6045 |
rs546562486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053530 | CTTTCTTTTTTCTTT[A/C]TTTTTGTAGAGATCG | 6045 |
rs546565981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050054 | GAGTCTGGGAGGGTA[A/G]TTTTGGAGTTGAGAG | 6045 |
rs546654744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085349 | GAGACGGGGTTTCAC[C/T]GTGGTCTCGATCTCC | 6045 |
rs546664914 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081335 | GAAGAAGTGGTAGTT[C/G]GTTGGCGAGAGGTCC | 6045 |
rs546672672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089464 | TACCAAGGGTCGACC[A/G]TATATACTTGGTGAC | 6045 |
rs546690037 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069469 | TCTAAAAAAAAAAAA[A/C]AAAAAAGAAATGCAG | 6045 |
rs546718793 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062218 | TCTCATTGCCATGTT[A/C]ATATTTTGTAACCTT | 6045 |
rs546730266 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062246 | CTTATTAAGGAATTT[A/G]TACACTGTGTATACC | 6045 |
rs546743256 | in-del | -/GA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057945 | GCTTGGCAACATGGT[-/GA]GAGACCCTGTCTCTA | 6045 |
rs546746285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087293 | GTCTGGTGAGGGCCT[A/G]TTCCTTATAGCTGCT | 6045 |
rs546750513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047162 | TAAGGATTGTAGTTA[C/T]TTTCCTCAGGTATCC | 6045 |
rs546765467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082626 | TCCCAAAGTGCTGGG[G/T]TTACAGGCGTGAGCC | 6045 |
rs546871492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063330 | AGATACTGATTCAGT[A/G]AGTCTGAAATGCAAC | 6045 |
rs546894800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056532 | CCTGGCTCATTTATT[A/T]TTTTTTATTTTTTAT | 6045 |
rs546899004 | in-del | -/ATA | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185047990 | TTGGGGTACAAAGGT[-/ATA]ATAATAGCATTTACA | 6045 |
rs546903086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080882 | AATTTTCCAGGGTAG[C/T]GTTCAGTAGGCAGAA | 6045 |
rs546956378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048196 | AGTGTTAGTGTGTTG[C/T]CAGGCAGGAGCTAGG | 6045 |
rs546986436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053762 | GGTACGTAATAGGCT[C/T]TCAATAAATATCTAA | 6045 |
rs547023214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060085 | ATTTCTCTACCCAGG[A/G]AAGGATAACAATCTT | 6045 |
rs547073445 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085820 | CACCACACCCGGCTA[A/C]TTTTTGTATTTTTAG | 6045 |
rs547198970 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185062628 | AGAAGAAAAGTACAT[A/T]AAAAATATATAAAAG | 6045 |
rs547255442 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185053221 | CCATAAAAAAATCCC[C/T]TTCATAGTCTCCCCA | 6045 |
rs547295012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059510 | AGTGTTATCTCTAAT[C/T]ACATTACAAGTACTT | 6045 |
rs547310968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096474 | CTCCCCCCAGTTCCC[A/G]GTAACTGTCATTCTA | 6045 |
rs547344924 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049582 | GAATTATTGTTTTAC[A/C]ATGTGCTAGGGTACA | 6045 |
rs547375684 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100683 | TTTTAGTCATACAGA[A/C]TGTTAAATATTATGT | 6045 |
rs547375923 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052474 | CAGCCACAAAAGGCC[A/G]CATATTACATGAGTC | 6045 |
rs547468074 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185068196 | TAAGGAAACAGCATG[C/T]ATGCAGGATAAAGAC | 6045 |
rs547520963 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102158 | AGTATGGGAGGATAT[A/G]AACTGCATCATTAGT | 6045 |
rs547543576 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185079944 | AGAAAAAAAAAAAAG[A/C]CAATTGTGTCTTTAA | 6045 |
rs547544251 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075160 | ACCACACCTGGCTAA[-/T]TTTTTTTATTTTTAG | 6045 |
rs547578824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061392 | AAAAGGGAAACAGAA[A/G]TGAAAGCTTCTGATC | 6045 |
rs547603450 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185076729 | TAAATTCACATATCT[A/G]TTTTTGAGCCCTTTG | 6045 |
rs547629266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073085 | TTTTTTACTTAATGT[A/G]TGTTGTATACATATA | 6045 |
rs547631028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079501 | AGCATCTTTGAAACA[A/C]CCAGTCTGCTTTTTG | 6045 |
rs547703896 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075301 | ATTGTGTATTTCTTA[C/T]AGCATGTCCATAGAG | 6045 |
rs547799382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067779 | GCAGTGATGCAATCT[C/T]GGCTCTCGGCAACCT | 6045 |
rs547878697 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185054847 | GGACCACAGGCGGGC[A/G]CCGCCACGCCCGGCT | 6045 |
rs547917528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054471 | CTGGCAAGCAGGCCT[C/T]CTTCTCCCATCTGGG | 6045 |
rs547938678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185082454 | CTCCCAGGTTCAAGC[A/G]ATCCTCCTGCCTCAG | 6045 |
rs548025840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185081888 | TCAGAAAACTGTAGT[A/G]GATCAGAAAGCTGTA | 6045 |
rs548079262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185079423 | TTCTAGAAAATAGGA[A/G]ATTATAGTCAGCCTG | 6045 |
rs548095420 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057538 | TACCTGTTGTCCCCG[A/T]AAGTTTACCTTTCCA | 6045 |
rs548166839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063975 | GATAATCTCCCCATC[C/T]TAAGAGCTGTAATTT | 6045 |
rs548168757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076438 | TGGGACTACAGGCGC[A/G]TGCCTCCATGCCTGG | 6045 |
rs548320944 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185075816 | GGATTATAATTCCAC[A/G]TGAGATTTGGGCGAA | 6045 |
rs548324132 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064530 | CTGCATCTGGATAAC[C/G]CATCTTAAATTGAAA | 6045 |
rs548325953 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057396 | TGATTAATATTTTAG[G/T]TGTATGAACCATAGT | 6045 |
rs548406743 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093892 | CAAAATCTGTCTCCA[A/G]ATTATCTTACTCAGT | 6045 |
rs548464212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090625 | AAAGCACAAGTATGA[C/T]GGACTGCCAGTGGAA | 6045 |
rs548504933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097822 | TTACAGGTGTGAACC[A/G]CCGTGCCTGGCCAGT | 6045 |
rs548550450 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185071993 | AGTAAGACATGAATA[A/G]GTAGATGTGGAGACA | 6045 |
rs548720736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078612 | TGAAGGTGGCCTGGC[A/G]CAGTGGCTCACTCCT | 6045 |
rs548733622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098663 | TACCACTGTATCTCC[A/G]GCACACTGCTTGCTG | 6045 |
rs548745579 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077823 | ATGCCTGATTCATTG[-/T]TTTTTTTCAGTCATT | 6045 |
rs548819219 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099196 | AGCTGGGATTACACT[C/T]ACCACAACACCTGGC | 6045 |
rs548838376 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043896 | GCGATCTCGGCTCAC[A/T]GCAACCTCTGCTTCC | 6045 |
rs548848546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091422 | GAGCTGTAGGCGATT[A/G]TAGTTGAAACAAAAT | 6045 |
rs548909342 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070506 | ATGTATGGCCCAGTC[-/AG]AGGATTATTTGAGAG | 6045 |
rs548960656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056323 | GCCAGTGAAAAAAAA[A/T]TTTACAAGATAAATT | 6045 |
rs548968191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080848 | CTTCAGCAGAATGTT[G/T]TATTTGATAGTTCCT | 6045 |
rs548997510 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185063242 | ACAGAATACGTAGAA[C/T]AGTGGTTCTCAAAAC | 6045 |
rs548998585 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185095191 | AAGGACTTTAATGGT[A/T]GTTCAGTTTAGCCTT | 6045 |
rs549005003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185087165 | TACTTCCTATCTTAA[C/T]CCATTTAGCCTGCTA | 6045 |
rs549020662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054805 | CGGGGTCAAGCGATC[C/T]TGCCACCTCAGTTTC | 6045 |
rs549030607 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044563 | AGCTACGCAATCTAC[C/G]TAAGTCACATAGACA | 6045 |
rs549035455 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102579 | TCTGTGTGCAATTAA[A/G]GTAATGCATTTCTCT | 6045 |
rs549044959 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074413 | ATCTTGTGGTTGGTT[A/C]TCCTGAAAACCAGTC | 6045 |
rs549077790 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096433 | TGAAACCCTGTATCC[A/T]TTAAGCACTAACTCC | 6045 |
rs549080522 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185081184 | AGTCAACACATTTTT[A/G]CCAATGAGAAATAAG | 6045 |
rs549155706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185054413 | GCTGGACACTGTGCT[C/T]TGTGTCCTGGGGCAC | 6045 |
rs549209858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068527 | AGAGGCAGATTGGAG[G/T]GATATGGTCACAAGC | 6045 |
rs549231903 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185060746 | AGAAGATGAAAAAAT[C/G]TAGCCTGGCAGATGA | 6045 |
rs549285503 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185062538 | ACCTATCCTCTTTAC[A/G]TGTAAAAAAAAATTG | 6045 |
rs549291253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185086475 | ATCGGGAAAGGAGGC[A/G]GAATTAATCAGCGTG | 6045 |
rs549351085 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048779 | AGTAAAAAAAAAAAT[C/G]ATGCTTGAAAATCCC | 6045 |
rs549366584 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095888 | TCTTTTTTGTTCCTC[A/C/G]TATGACACTCAAGAT | 6045 |
rs549425143 | in-del | -/C | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185075895 | TGTCAATATCACAGA[-/C]AAAAAATAGAGCCTA | 6045 |
rs549456655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092322 | GCTGGGATTACAGGC[G/T]TGTATCACCACGCCT | 6045 |
rs549510460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052330 | CCCAAATGTCTGTCA[A/G]CAGATGAATGGATAA | 6045 |
rs549524313 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185071776 | CAGTAGTGACTGATT[C/G]ATGCTTTTTTCCAAG | 6045 |
rs549528706 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF2 | GRCh38.p7 | 1:185098877 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 6045 |
rs549626443 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185072456 | AGAGGCTATAAAAGT[G/T]CTATGGTTAAGAAAA | 6045 |
rs549687595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065253 | GTGTCTAGCTAAAGG[A/G]TTGTAAATGCACCAG | 6045 |
rs549712106 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044883 | AGGTAACACTGGAAG[A/G]GGCCAAGGAGGTAGG | 6045 |
rs549712470 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074941 | GAGGGTGTCCTGGAA[C/T]CAATCCCCCTTGGAT | 6045 |
rs549748807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185059430 | GAGGGAAAAAAGTAC[C/T]GAGTCCATATCACCT | 6045 |
rs549871796 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044844 | ATCTATTAATCTATT[A/T]CTTCGTAAATCCTCA | 6045 |
rs549929250 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085779 | CTACCTCATCCTCCC[C/G]CATAGCTGGGATTAC | 6045 |
rs549968281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085397 | TGCCTCGGCCTCCCA[A/G]AGTGCTGAGATTACA | 6045 |
rs549968354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093378 | ACAGTAACAAATAGT[A/G]GTACTGCATGATTAC | 6045 |
rs549988327 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185077860 | TTATTATTTTAAAAT[C/T]GCAGGTTATAAATAT | 6045 |
rs549998042 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046133 | GGTGGGGTAGGGGGC[A/G]CTTTGTGCAGATATC | 6045 |
rs550044275 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100408 | TGGATATGTTGTTCA[A/G]TTTTCTTTCTGAGCC | 6045 |
rs550195024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072889 | AAGTTGCAGTGAGCC[A/G]AGATTGTGCCACTGC | 6045 |
rs550317896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060253 | CTTAGTTGTGTTTCA[C/G]ATATCCCTCACAAAG | 6045 |
rs550325723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088805 | GTGCTAATAAGTACT[A/G]TGTTGAATCCATGCA | 6045 |
rs550364190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185087984 | ATAAGTACTGATAAG[A/G]CACCAAGGAAGACTG | 6045 |
rs550381027 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045361 | CTCCAGGCCAACACG[C/G]GGCGGCGCACCCTCC | 6045 |
rs550501367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076390 | CCGTCTCCTGGCTTT[A/G]AGTGATTCTCCTGCC | 6045 |
rs550542773 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060812 | GTCTTGTCAGAGGGA[C/G]AGACAGTTAAGAATT | 6045 |
rs550555745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070400 | TTGTTGTTTTATAAC[A/C]TAAAGGGATCCCTAA | 6045 |
rs550607818 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185095222 | TTACTAAAAGCAAGA[C/T]TCTCCTTGTAAATAT | 6045 |
rs550653404 | in-del | -/GCG | 0.0130921 | 0.0798413 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045564 | GGCTCGCCATATTGT[-/GCG]GCGGCGGCGCCGGCG | 6045 |
rs550716885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081358 | AGAGGTCCGATGACT[A/G]TGGTGGGTGAGGCAA | 6045 |
rs550719369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070842 | TGGGTTTCACCGTAT[G/T]AGCCGGGATGGTCTC | 6045 |
rs550719691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063370 | AGAATTGTTTAAAAT[C/T]TCATCCAGATGAAAG | 6045 |
rs550774616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185049179 | TGCAGTGCATGCCAC[C/T]GCACTGCATCCTGGG | 6045 |
rs550781684 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082926 | AACCACATTGAAGAA[C/T]GTATTCCAGTATCAA | 6045 |
rs550795701 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098012 | GCAAACATGCTTCAG[A/G]TTTGTTGCTTTAAAG | 6045 |
rs550818651 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085662 | TCCTGTTTAAAACTT[C/T]TTTTTTTTTGAGACT | 6045 |
rs550837802 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075087 | GCAACCTACACCTTC[C/G]GGGTTCAAGCCATTC | 6045 |
rs550889146 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065179 | TCAGCCCTCTGTGTC[C/T]AGCTAAAGGATTGTA | 6045 |
rs550891933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057299 | CTGGGCAACCCTGTT[C/T]CAAAAAATAAATAAA | 6045 |
rs550915451 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094246 | TCCTGGGTTTCCAGC[A/G]ATTCTCCTGCTTTAG | 6045 |
rs550943080 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046361 | TCTGCGGGAAGATTC[G/T]CGTTTTGAACCGTGT | 6045 |
rs550999141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090594 | TGTGGAGTAATCCAT[C/T]TTTGACCATATAAAG | 6045 |
rs551030211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084209 | CACCATAGCCACCCA[A/G]TCTTTAAGTCTTCTA | 6045 |
rs551092199 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085856 | ACGGTTTCACCATGT[A/T]GGCCAGGCTGGTCTC | 6045 |
rs551138228 | in-del | -/TA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095671 | CAGTAAATATTTATC[-/TA]TGTGTGAATTTTTAA | 6045 |
rs551210522 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185063439 | TCTAGAGGAAGACTC[-/T]TTTCCTGTGAGTGCA | 6045 |
rs551227657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051271 | CCAAATGTTTTCTAG[A/G]AGGCTTTACTGTATT | 6045 |
rs551228087 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045667 | GAGTGGGGCGGGCGG[C/G]GAGGCGAAGGACGCG | 6045 |
rs551289589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185090008 | CTCACTGCAACCTCT[A/G]CCTCCCAGATTCAAA | 6045 |
rs551289647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097684 | GATGATAGGTGCACC[A/G]CCACGCCCAGCTAAT | 6045 |
rs551326368 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185097143 | TTCTCAACTAGAAAA[C/T]GACATTAATGGTAAC | 6045 |
rs551333685 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098954 | ACAGGGTTTCACCAT[A/G]TTGGCCAGGATGGTC | 6045 |
rs551349690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054334 | GAACTGTTCACATAC[A/G]TAACCGGCAAGTGGC | 6045 |
rs551419674 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070202 | CCAGGTACTTCATAT[C/G]AATATCTCATTCAGT | 6045 |
rs551427057 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095654 | TTAAAGTAGTAGCTG[C/T]TCAGTAAATATTTAT | 6045 |
rs551433708 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185080135 | TTTGCTGGCTTCCAC[G/T]CTACTCTTCAGCTTT | 6045 |
rs551450561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095763 | ATGTTGAAATACTTA[C/T]GTTGACTTCTACATA | 6045 |
rs551490133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095328 | TTACAGCTTCCTTAC[C/T]GTTCTTCAGACTCAC | 6045 |
rs551587513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055573 | GCGAGCGCCACCACG[A/C]CCAGCTAATTTTTGT | 6045 |
rs551607316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073722 | CAGTACATTTTTATT[G/T]TATGTCAATCAAAGA | 6045 |
rs551681660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068445 | TAAATGTTACCACAT[A/G]TAACTTTATAAGAGA | 6045 |
rs551689396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093569 | TTTATGAACCCCCTC[A/C]AATCAGACATTCATC | 6045 |
rs551691195 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101787 | AAGGTATATATTCAA[G/T]TTTTTACCATTTTAT | 6045 |
rs551725907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080726 | TTCTGGAAATGCAAC[C/T]AACTTGTCAATCACT | 6045 |
rs551726551 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100715 | TTCTGACTTTTTTTT[C/T]CCCCCGGAGTCTTGT | 6045 |
rs551750078 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185054881 | TTTTTTCTATTTTTG[G/T]TGGAGACAAGGTTTC | 6045 |
rs551845848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185098754 | TAAAAATCCTCAAAT[C/T]AACTTTTTTTTTTTT | 6045 |
rs551914492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185077229 | TGGATTTTATAGTTA[A/G]CTATCATTATTTGCA | 6045 |
rs552002468 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185076596 | CGGCCTTATTTTATG[G/T]TTTTTTTTTTTATGT | 6045 |
rs552070168 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098838 | CTCACTGCAGCCTCC[A/G]CCTCCTGGGTTCAAG | 6045 |
rs552139695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065183 | CCCTCTGTGTCTAGC[G/T]AAAGGATTGTAAATG | 6045 |
rs552226882 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081342 | TGGTAGTTGGTTGGC[A/G]AGAGGTCCGATGACT | 6045 |
rs552264841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052225 | CTCCTACCACTAAAC[C/T]GGAGGTATCCAAAGT | 6045 |
rs552302922 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051417 | TTTGTTAAAAAAAAT[A/T]AAAAATGCCAGCCTC | 6045 |
rs552351266 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081955 | TTTTGGTGCATGTTT[C/G]CCGTTGGGAAGTGCT | 6045 |
rs552458035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084540 | AATCTTCTAGGGATG[C/T]TGTTTTCAAGTCAGT | 6045 |
rs552555018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072361 | AGCAAATATTTATTG[A/G]ATGACTACTATATGC | 6045 |
rs552563606 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078346 | GATTCTTATGAAGAT[G/T]ACCATCTTGGCTTCT | 6045 |
rs552647578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068710 | AACTTACTGTTGTTA[G/T]AAGCCTTCAAATTTG | 6045 |
rs552653886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078724 | AGACCAGCCTGGCCA[A/C]CATGGTGAAACCCCA | 6045 |
rs552711772 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185092245 | GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT | 6045 |
rs552717736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072837 | CCCAGCTACTTGGGA[A/G]TCTGAGGCAGGAGAA | 6045 |
rs552784987 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043948 | CCTCAGCCTCCCGAG[A/T]AGCTGGGACTGCAGG | 6045 |
rs552806699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061800 | GACTGTTTTTAGGCA[A/G]TGTACTGTCAGAAAC | 6045 |
rs552883661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061252 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 6045 |
rs552904824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086575 | AGGAAAATCAGGTGG[G/T]ATATGATACCACTTT | 6045 |
rs552912533 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185075183 | ATTTTTAGTAGAGAC[G/T]GGTTTTCGCCGTGTT | 6045 |
rs552942410 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044706 | CATGACATCTCAACA[A/C]TAGTACATATAGAGA | 6045 |
rs552949670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081506 | TCAAGTGATTATCCT[A/G]CCTCAGCCTCCTGAG | 6045 |
rs552951017 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185056369 | TTTTTTTTTTCTCAT[A/T]TTTTTTAGAGACAGG | 6045 |
rs553020085 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185086438 | GCAGAGAAGTTGGTC[A/T]TATGCTCTTCAGTTC | 6045 |
rs553025202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075963 | ATTAGTGAAGTTTAG[C/T]ACAGTTTAATTTTAT | 6045 |
rs553048410 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054434 | CCTGGGGCACGTCTG[A/G]TGATAGCTGGGCCTT | 6045 |
rs553056675 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103060 | CTTTTTAAAATAACT[A/G]TATTAATGGGTATCC | 6045 |
rs553139457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055763 | ATCAGATTCAGAAAA[C/T]CTCTGCTTTTAAAAA | 6045 |
rs553143820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047753 | CTGGATAAACTAAAA[A/G]TCCATCACAGTTTGC | 6045 |
rs553176509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055031 | TTGCATGTGTTGATT[G/T]TATCTTGAGAGAACA | 6045 |
rs553177464 | snp | A/G | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185080245 | TGACTCTCAGATATT[A/G]TTCATTGAAATCACT | 6045 |
rs553216012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079757 | CAACATGGCAAACCC[C/T]GTCTCTACTAAAAGT | 6045 |
rs553258069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185048575 | TAAATTTTCTAATGA[C/G]AGCATACTATTAAGT | 6045 |
rs553260363 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185052910 | GGCTGTACTACAGCT[-/AC]AGTGCTTAATATGAG | 6045 |
rs553306642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081985 | TTTGGAGCTTTGGAA[A/G]TGCTTCAGTCCAACC | 6045 |
rs553332844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084031 | ACTGAAACTTTAAAC[A/T]CCTGGGCTCAAGCAA | 6045 |
rs553371530 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185065184 | CCTCTGTGTCTAGCT[A/G]AAGGATTGTAAATGC | 6045 |
rs553379689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088261 | ATTTAGAAATTAGGT[A/G]ATGGACAAGGAGCCA | 6045 |
rs553435842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078938 | AATCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA | 6045 |
rs553542198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185058845 | AGATATCACTTAAAA[C/T]GTGCTCATTTTATAG | 6045 |
rs553542452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051817 | ATTTTTACATATATA[C/T]ACACACATTTTATGT | 6045 |
rs553574553 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083012 | ACAAAGAAGCTGGCC[A/G]TCTATATTTATACAT | 6045 |
rs553771890 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101227 | ATTTTTTTCTTATTT[A/G]TAGCCACATAAGTTT | 6045 |
rs553972435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094761 | TTTTTAAGACCCTAT[A/G]TAAGGTGGGCATTTT | 6045 |
rs553998560 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044243 | CAAGCCACTGAAAAA[G/T]AATAATGCTTGTTTT | 6045 |
rs554071960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185098993 | TTGACCTCGTGATCC[A/G]CCTGCCTTGGCCTCC | 6045 |
rs554111583 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078685 | GAGGCCGAGGTGGGC[A/G]GATCACCTGAGGTTG | 6045 |
rs554154135 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101337 | AGTTTATAAATTTGG[C/T]GCTCTTTTAATTACA | 6045 |
rs554185517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185067211 | CAGTACAGTGACAAG[C/T]TTTTCAGTAAAGAAC | 6045 |
rs554201505 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185053995 | CCTGTTAATCTACAT[C/T]CCCCCCCCACCCAGT | 6045 |
rs554233974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053456 | CCTCCCGCCTCAGCC[A/G]CCTTTGTAGCTGAGA | 6045 |
rs554237957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185085966 | CCTGTTTAAAACTTT[C/T]AGTATCTTCCAATCA | 6045 |
rs554239863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046015 | TCCGGGGGCGGGGGC[C/T]CCAGCCTCTCTGCAG | 6045 |
rs554293133 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185066347 | ACTACTTGGAGTTTC[C/G]CAGACATGCCATGCT | 6045 |
rs554371403 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185049721 | GTAATCAGAACCTAA[G/T]AGCTCAGAGAAGAGG | 6045 |
rs554496881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064389 | ATTTCATACTCTGAT[G/T]TTTTTGGTAATGCTT | 6045 |
rs554510526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075141 | CTGGATTACAGGCAC[C/G]CATCACCACACCTGG | 6045 |
rs554584487 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185054282 | GGCGGAAAACGAACC[C/T]CCAGTTTACAGGTAA | 6045 |
rs554595954 | snp | A/G | 0 | 0 | intron-variant | RNF2 | GRCh38.p7 | 1:185056624 | GATCCTCCCTCCTTG[A/G]CCTCCCAAAGTGCTG | 6045 |
rs554634390 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092046 | GCCAGGTTTCAGCAT[A/G]TTGAACTCCTGACCT | 6045 |
rs554635270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055993 | ATGTATGTTTTTAAA[A/G]GCTCTCAAATATTAA | 6045 |
rs554704513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089463 | ATACCAAGGGTCGAC[C/T]GTATATACTTGGTGA | 6045 |
rs554903680 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071515 | TAAGCTTAACTTCCC[A/C]TTTGGCATCGTGCGT | 6045 |
rs554918562 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185062821 | GACCTCCCCCCCCCC[A/C]AAAAAAGGCCAATAA | 6045 |
rs555004620 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046126 | TCGTGGGGGTGGGGT[A/G]GGGGGCACTTTGTGC | 6045 |
rs555024276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185073097 | TGTGTGTTGTATACA[C/T]ATATTGAGTTCTGTG | 6045 |
rs555027502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067885 | CCAGCTAATTTTTGT[A/G]TTTTTAATACAGATG | 6045 |
rs555032694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073821 | TGGTTTTTTGCTACA[C/T]TAACAATTCTCCAAC | 6045 |
rs555044499 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084292 | GTTTATGTTGGCTTA[A/C]CACTCGAATCAGCAT | 6045 |
rs555074226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080225 | TGTTAGTATCTATAC[A/G]TAGGTGACTCTCAGA | 6045 |
rs555152466 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185090058 | TCCCAAGTAGCTGGG[A/C]TTACAGGCGTGTGCC | 6045 |
rs555179185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050352 | ACTTGCCTCTTCTCT[C/G]CCTACCTAACTTTAT | 6045 |
rs555285739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185076726 | CCCTAAATTCACATA[C/T]CTGTTTTTGAGCCCT | 6045 |
rs555292303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185066336 | TTTAATAGTGAACTA[C/T]TTGGAGTTTCCCAGA | 6045 |
rs555313225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081017 | CTCCTGAGTAGTTTT[C/G]GTTCTCTGAAAGATC | 6045 |
rs555423777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185081486 | GCAACGTCTGCCTCC[C/T]GGGTTCAAGTGATTA | 6045 |
rs555475102 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093692 | GCAGCATTTGACACA[A/G]TTAATTTCTCCCTTC | 6045 |
rs555499693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185061596 | TCTCTTTAAGACAGA[A/G]TGGGAAAAAAACGGC | 6045 |
rs555571279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085871 | TGGCCAGGCTGGTCT[C/T]GAACTCCTCACCTCA | 6045 |
rs555572935 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045095 | GCAAACCAAAGCCTG[A/T]TGAGGATTTCCGCCG | 6045 |
rs555586361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061124 | AGACCCTATTTCTCT[C/T]TCTCTTTTTTTTTTT | 6045 |
rs555591370 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067970 | CGCCTTGGCCTTCCA[A/G]AGTGCTGGGATTACA | 6045 |
rs555606409 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185085570 | ACTTTCTCTCACTGA[C/T]TTTATTGTTAGTTGC | 6045 |
rs555608298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093687 | ACTTAGCAGCATTTG[A/G]CACAATTAATTTCTC | 6045 |
rs555778582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095407 | AGGAACCTTCTTCCA[A/G]ATAATCCACATGGCA | 6045 |
rs555806805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054987 | TTACAGGCATGAGCC[A/G]ATGCACCTGCTGTTT | 6045 |
rs555810515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074729 | ACAGATTTTTTTTCT[C/T]GTGTCATTATTCTCT | 6045 |
rs555888700 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185054671 | CTCAGTTTCTTTTTA[A/G]TCTTTCTTTGTGGGT | 6045 |
rs555901451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064716 | TCAAATCCATGAACA[C/T]GGGATGTCTTTCCAT | 6045 |
rs555978370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077585 | TTAAATCTCATATCC[A/G]TACATATGTGTGGTT | 6045 |
rs555985546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064281 | TAGGTTGGATAGGAT[A/G]GGATAGCTAGTCTTA | 6045 |
rs556012998 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102512 | TTCACAATGTTGTGT[A/G]ATGATCACCGCTGTC | 6045 |
rs556048559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046637 | TGTAAAATGATTTGA[A/G]GATGTCAGGTTTCTT | 6045 |
rs556161179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051664 | GGTGTGGGAGGAGTT[A/G]TGGATGTCCTATAAC | 6045 |
rs556190081 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043535 | CTTTTTTAAGCACTA[A/T]ATTTAACTTTCATCC | 6045 |
rs556203143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050761 | ACCAATAGGTGATCT[A/G]AAAATGGGGCTTTGG | 6045 |
rs556219187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185097517 | TTTGTCAATTAATTC[C/T]TATAGTCTTTTGTTT | 6045 |
rs556238184 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066644 | AATGTTTCCTAAATG[C/G]TTGAACTCAACTGGT | 6045 |
rs556276928 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068594 | TAAGGAACAGATTCT[A/C]CCCTAGGGCCTCTGG | 6045 |
rs556302001 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044134 | GCCTTTTTTTCTCCC[C/T]CCACATTGGAGGAAG | 6045 |
rs556376430 | snp | C/T | 9.88647e-05 | 0.00703012 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098105 | ACAACAGATTGAAAA[C/T]GGTAGTGGAGCAGAA | 6045 |
rs556378814 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101056 | ATATAGTCTTCAAGT[A/G]TACGTTTGAGAGTGC | 6045 |
rs556563581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072455 | TAGAGGCTATAAAAG[C/T]GCTATGGTTAAGAAA | 6045 |
rs556635205 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062811 | ATAATTGGTAGACCT[-/C]CCCCCCCCCAAAAAA | 6045 |
rs556638004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185053382 | GCTATGTTGCCCAGG[C/G]TGGAGTGCAGTGAGG | 6045 |
rs556640593 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185059220 | GTCTCCTGAATCCCA[A/G]TCTGGATTAAAAAAA | 6045 |
rs556645235 | snp | C/G/T | 0.00279242 | 0.0372774 | intron-variant | RNF2 | GRCh38.p7 | 1:185062818 | GTAGACCTCCCCCCC[C/G/T]CCAAAAAAAGGCCAA | 6045 |
rs556721879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078236 | TGGGTGACAAAGTGA[A/G]ACTCCATCATAAATC | 6045 |
rs556802582 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | RNF2 | GRCh38.p7 | 1:185055850 | TTGTCCTTGATCTTA[A/C]AATTTTTAGTTAGCA | 6045 |
rs556877612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185065605 | CTGTAACACTCACTG[C/T]GAAGGTCCACAGCTT | 6045 |
rs557017438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063678 | CAAAATGAGTCTTAC[A/G]GGATTGAAATTAAGG | 6045 |
rs557019591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071050 | GTTTGCCAAGTAATA[C/T]AAAGTGAGTATTTGT | 6045 |
rs557048796 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096138 | GTAATTTATGGTCAA[A/T]TAACTTTTCATTTGC | 6045 |
rs557080400 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057723 | GAGTGTCTAAGGATC[C/T]ACAAATACAGTCATC | 6045 |
rs557164761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048795 | ATGCTTGAAAATCCC[A/T]CAGGAAGGCAGAACA | 6045 |
rs557191305 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055909 | TTAGTGCAAAAGTGC[-/T]TTTTTTTTAATGTAG | 6045 |
rs557201991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073959 | GCCTCCACTTCAGAT[A/G]CCATTAAGCCCATGC | 6045 |
rs557277857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068882 | AGCTTTATTTCAGAT[A/G]CTCTGTATAGACCAG | 6045 |
rs557293764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087443 | CCTCTTAATATTACT[A/T]CATTGAGATTAGATT | 6045 |
rs557303826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072555 | GAAAATCTTGGGGGG[A/G]AGAAATCATTCCTTT | 6045 |
rs557326838 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058968 | ACCTAAATATTGTGC[C/T]AATTTTAGATTTATC | 6045 |
rs557328758 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089829 | GAGGTCAGGAGTTTG[C/T]GGCCAGCCTGGCCAA | 6045 |
rs557362356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185082012 | AACCACTGAGCGGGT[C/T]GTCACTAGTTACCAA | 6045 |
rs557433496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079594 | GAACAGTCATTTTAT[C/T]TTATAAAATGAGATG | 6045 |
rs557515505 | in-del | -/AAA | 0.0495626 | 0.149415 | intron-variant | RNF2 | GRCh38.p7 | 1:185049671 | GGTTAGATGAGTGTA[-/AAA]AAAAAAAAAAAGCGG | 6045 |
rs557520972 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044410 | AATTGATATTTTTCT[A/T]TTCCAAATTCCTATG | 6045 |
rs557559269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052652 | GACTGTGAATGCGCT[A/G]AATGCCACTAAATGT | 6045 |
rs557605878 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185096561 | ATTTGTACTTTTGGG[G/T]TTTTTTTTTTGTTGT | 6045 |
rs557634593 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045022 | TTATCCTGCAAGGAT[G/T]AAAAGTGTATGTTTG | 6045 |
rs557697668 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085718 | GAGTGCAATGGCGCG[A/G]TCTCAGCTCACTGCA | 6045 |
rs557718060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089311 | TGTCCATGGCCTGAG[G/T]TTCGGGACCCCTGAT | 6045 |
rs557719281 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062906 | AAAGAAGTATCATTT[C/T]CCTCCCACTTATCAG | 6045 |
rs557906781 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058343 | TATCTTCAGAACCCC[A/G]TGGATACTCAGGGAG | 6045 |
rs557985014 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102273 | GTGTGTTTTGGGGTA[C/T]GGGGAGAGGCGATGC | 6045 |
rs557996256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185100026 | ACTAACTGAGTGGCA[A/G]GTGGTGGGGTAGAAT | 6045 |
rs558022799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085497 | TCTCTAATTCCGTCT[C/G]TGTGTCCATGTTTAA | 6045 |
rs558072697 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101348 | TTGGCGCTCTTTTAA[C/T]TACACTCTGTAGAAG | 6045 |
rs558110863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092475 | CCACCGTGCCTAGCC[A/G]AGAAATACATTTTCT | 6045 |
rs558144078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097351 | GTCAGCAGGGAGGAA[A/G]TACTTACTATTCTTC | 6045 |
rs558144937 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063830 | TTCCCAGTGTCTTAG[A/T]TTGCTCTCTTGGACT | 6045 |
rs558222998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080461 | CTAATTCTCAAGAGT[A/G]TATCTGTTCAGTGAC | 6045 |
rs558260046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086729 | TCTGAACATGAGGTC[A/G]GGAATTTTTCATGAG | 6045 |
rs558268936 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056027 | ACTATCTAGAATAGT[A/G]AATCTAAATTTCTTT | 6045 |
rs558290623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060426 | GTTCCTATTATCTGA[A/G]TAGGGATATGAACTG | 6045 |
rs558295172 | in-del | -/ATTG | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185068654 | TTTTGGCCCAGTGAT[-/ATTG]ATTGAATTAGGACTT | 6045 |
rs558320775 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083288 | TAGTTCGTATTTTGT[C/G]AGTTTTCTCAGGTTC | 6045 |
rs558357459 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185082883 | AAAACATAAAGTGAG[A/T]AATGCCCATTAAAAT | 6045 |
rs558381998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096691 | AGCATGTCTATTCAT[A/G]TTGTATGTGGCAGGA | 6045 |
rs558397623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090141 | TGGTCAGGCTGGTCT[A/C]GAACTTCTGACCTTG | 6045 |
rs558420117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063643 | AACTTACTATTTTAC[A/G]GTTCTGGCAGTAAGA | 6045 |
rs558447889 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185054045 | AATATGGCATTAAAC[A/G]TCTTCACAAATGACT | 6045 |
rs558510201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070662 | TTTTTTTTTTGAGAC[C/T]GAGTCTTGCTGTGTC | 6045 |
rs558536633 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079854 | AGAATTGCTTGAACC[C/T]GGGAGGTGGAGGTTG | 6045 |
rs558551040 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057484 | GTTCATGATAAGCAC[C/G]TCCATTATTCATGTG | 6045 |
rs558615734 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185049748 | GAGGTTCTATGGACC[C/T]GGTGCTGGACTTTTG | 6045 |
rs558633013 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060735 | AACATCCTTGGAGAA[C/G]ATGAAAAAATCTAGC | 6045 |
rs558640076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058285 | TTTTATTTATGTAAG[A/G]GATTTGAATATCTGT | 6045 |
rs558826168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064176 | ATATCATATTCTAGC[C/T]CTAAATAAATTAGCT | 6045 |
rs558874508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054306 | CAGGTAAGGAAATGG[C/T]GGCTTAAGTTCAGAA | 6045 |
rs558906024 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185056984 | ACATAGTTTTAACTG[C/T]ATTTTATATGTAGAT | 6045 |
rs559015291 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050386 | TACTCTTTTTATCTT[A/C]TATCCTGATTAAATC | 6045 |
rs559021929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076534 | CTTGTGATCCACCTG[C/T]CTTGGCCTCCCAAAG | 6045 |
rs559035960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054692 | CTTTGTGGGTTTTTT[A/T]AAATTTTTTATTATT | 6045 |
rs559042572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185071956 | AAATGTCATGGCAAA[A/G]CCATATCATTGTGGA | 6045 |
rs559158144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077453 | GTTTTGGGACTTCCG[A/G]TAGATTTTTCATGAG | 6045 |
rs559199353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060095 | CCAGGAAAGGATAAC[A/C]ATCTTGGAATATACC | 6045 |
rs559245758 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073475 | AGCAATTTTTAGAGA[C/G]TATTCCAGTCTGTTC | 6045 |
rs559282075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071536 | CATCGTGCGTTTAGA[A/G]TCCCGAGATTCTATT | 6045 |
rs559330878 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046531 | TTCCAGTTATTTGCC[C/T]GCTAAGATCAATTAT | 6045 |
rs559334419 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185074815 | AAGTAATCTAGAGAT[G/T]ATTTAAAGTACACAG | 6045 |
rs559353727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086379 | TTTTTATCTACAACC[C/T]TCTTTCCCATATTTA | 6045 |
rs559362305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067454 | AGGAAGAAATTATTT[G/T]CTCATTTACATTTGT | 6045 |
rs559367199 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101726 | CAGTTTTGACAGATT[A/G]GGGCCAGCTTGATGT | 6045 |
rs559377867 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077504 | TTTCTAACTTATTAC[A/G]ACTTTTATTAGAAAT | 6045 |
rs559383823 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080044 | ATCTTTAGGCTGTTG[G/T]GATCTAGGGAGCACA | 6045 |
rs559436658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094369 | GGCTGGTCTCAACTC[C/T]TGACCTTGTGATCTG | 6045 |
rs559449018 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097297 | TACCATCGCATTTTC[C/T]TCAGTCATTTTGTAT | 6045 |
rs559508230 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077502 | TATTTCTAACTTATT[A/G]CGACTTTTATTAGAA | 6045 |
rs559529957 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102356 | CTTTTATCACTATCT[C/T]AACTGAGGAAGAAAA | 6045 |
rs559551432 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185046758 | TTCTAAACCGAGGAT[A/G]TGTTTAAAACGAATG | 6045 |
rs559592809 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052648 | ACAAGACTGTGAATG[C/T]GCTAAATGCCACTAA | 6045 |
rs559606686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185081039 | TGAAAGATCTATCTA[A/G]GATATATGTTAGAAA | 6045 |
rs559708675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068268 | GTTATAGTCACTCTT[A/T]CTTTGGTCAGTGTGG | 6045 |
rs559709547 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185086961 | TAAGCACTTTTGATA[C/T]GCTAAGTACTTCCTG | 6045 |
rs559715611 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047733 | TTGAAATGACTCATT[A/C]AATTCTGGATAAACT | 6045 |
rs559722220 | snp | G/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102989 | ATTCCTGCCACCAAT[G/T]AACAAGCGTTCTGGC | 6045 |
rs559727931 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185077675 | ATTGGCTGTACCTGA[A/C]AACTAAATTGTACTT | 6045 |
rs560014952 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185077159 | ATTTTTTTTATCTTC[A/T]TTCCACCATGTTACT | 6045 |
rs560015911 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093517 | TTTATAGCAAAATTC[C/T]TTGAAAGAGTTGTAA | 6045 |
rs560052624 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185083124 | GCTTCTTTGTTTGCT[A/G]ATACGGAACAAAGCC | 6045 |
rs560059901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071648 | GCCAATCTTGGACAA[G/T]TTGAACATGGTCACC | 6045 |
rs560170124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065129 | ACGCACCAATCAGCC[C/G]TCTTTGTCTAGCTAA | 6045 |
rs560186137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185071925 | TATATTTTCTCTCCT[C/T]ATGACATTGGTGAAG | 6045 |
rs560224542 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043993 | CCTGGCTAACTTTTT[C/T]TTGTATTTTTAGTAA | 6045 |
rs560318441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090318 | GCCCTGGAGGAGAAC[A/C]TAGATGGTTGAATTT | 6045 |
rs560326602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050900 | ATCTCAAGGTATTTC[A/G]GTGTGGGATGGGGAG | 6045 |
rs560417848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085692 | TAAGTGTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 6045 |
rs560493915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085314 | CCACCGTGCCCAGCT[A/G]ATTTTTTGTATTTTT | 6045 |
rs560498839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098665 | CCACTGTATCTCCAG[C/T]ACACTGCTTGCTGTT | 6045 |
rs560524835 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091793 | TACCACGAAAGTGCT[C/G/T]TCCAGGGTTTGAGAA | 6045 |
rs560562670 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185065873 | TCTGTTTCCTTTTTT[C/T]CCCCCCTACTTGCTC | 6045 |
rs560563662 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074766 | TACCATATAACAATT[A/G]TTTACATAGCGTTTA | 6045 |
rs560567649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079204 | CCTACTTTGTATAGA[A/G]GCATTTCTGGTGTTT | 6045 |
rs560594438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185078718 | AGTTCGAGACCAGCC[C/T]GGCCAACATGGTGAA | 6045 |
rs560619226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052143 | TTCCTTCAGACCATT[C/T]CAGACTCATTCCTTC | 6045 |
rs560619231 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185059229 | ATCCCAGTCTGGATT[A/T]AAAAAAAAAAACCTC | 6045 |
rs560705066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058540 | CTGTAAAAAGTATTT[A/G]AAACAGTATCTGTTG | 6045 |
rs560749335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048103 | CTTCTGGTATTTCTT[G/T]GGGGAAGCGCAGTTT | 6045 |
rs560854326 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051225 | CTATATAGAGTCTTA[C/T]TCAGTCTGGGACGGC | 6045 |
rs560903625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057037 | ACCTGGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 6045 |
rs560913680 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070858 | AGCCGGGATGGTCTC[A/G]ATTTCCTGACCTCGT | 6045 |
rs560928817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048857 | TTGGAACACATTGCA[A/G]TTTCTTGGTGTTTCT | 6045 |
rs560952666 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044577 | CGTAAGTCACATAGA[C/T]ACACATTGGAGGCTA | 6045 |
rs561022041 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185062212 | TAGTGTTCTCATTGC[C/T]ATGTTCATATTTTGT | 6045 |
rs561109761 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061305 | GCTAATTTTTTGTAT[A/T]TTTAGTAGAGACGGG | 6045 |
rs561183342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055435 | TTGTTGTTGTTTTTA[A/C]ATTTAAATGGGTTCT | 6045 |
rs561271797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096992 | TATTCCTTTTTTCTT[A/G]TCTATACAGGTAGGG | 6045 |
rs561289831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070017 | CTCTAAAATAACTTA[C/T]TCTTTTGACAGAGTA | 6045 |
rs561299382 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059954 | TTAATTTGCCAACAG[A/T]CTGTGGCCTTCCCAG | 6045 |
rs561325905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075517 | TAACTCCCTGAGACC[A/G]GATAATTTATAGAGA | 6045 |
rs561408345 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185093394 | GTACTGCATGATTAC[C/T]TTTCGTGCAGGTATA | 6045 |
rs561441319 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095035 | AGTGTAGTCAAGATC[A/G]AAAACCACTGGCTTA | 6045 |
rs561463694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060554 | TCGGAGAATTAAAGG[C/T]AGTCCTTTATAAGAA | 6045 |
rs561505056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076057 | TAGTACTCAGTATAT[A/C]TTATCGTTATTGGCC | 6045 |
rs561590593 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101624 | TGTTTGCATTGAGAA[A/G]TTAACCCTAAAGGGT | 6045 |
rs561629860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066034 | CCTTTGTCATTTCCT[A/G]TATCCCATGTATTGT | 6045 |
rs561649631 | in-del | -/TGGG | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185069382 | GATTGCCTGAGCCCA[-/TGGG]GGAGGTCAAGGCTGT | 6045 |
rs561753551 | in-del | -/GA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088330 | GAAAAACAGGAGATT[-/GA]GAGAGAGGGGGGATT | 6045 |
rs561755589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080593 | CATGTGGTAGTATTT[A/G]AGACTGTAGATACCA | 6045 |
rs561870720 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100621 | CATAGTTTCTGTATT[A/C]TTATAAGATTCAGTT | 6045 |
rs561900617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185074016 | TAAGTTGGGGATTTC[C/T]GCAATCCCCTTGTCA | 6045 |
rs561927410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078552 | CAGCATTAGTAAGCA[C/G]TAATTCTTTCTGAGT | 6045 |
rs562006054 | in-del | -/AC | 0.00159617 | 0.0282053 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044576 | ACGTAAGTCACATAG[-/AC]ACACATTGGAGGCTA | 6045 |
rs562020157 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185068115 | TTCAAGCGATTCTCC[G/T]GCCTCAGCCTCCTGT | 6045 |
rs562038706 | in-del | -/AA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060564 | AAGGTAGTCCTTTAT[-/AA]AAGAATGTGATGAAT | 6045 |
rs562040963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086807 | AAGTAGATTTTTTAA[C/T]TTGGACAGCATTGGA | 6045 |
rs562041159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079917 | CCTGGGCAACAAGAG[C/T]GAGACTGTCTCAGAA | 6045 |
rs562117265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073483 | TTAGAGAGTATTCCA[G/T]TCTGTTCTTTTAGTG | 6045 |
rs562132702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046182 | GTCGGAGTCGGGGTT[C/G]CAGTGTAGAGGAGCT | 6045 |
rs562167585 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185094143 | TCAGTTTTTTTTTTT[A/T]ATTTTTTTTATTTTT | 6045 |
rs562173348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054197 | GGTAGAGCTGCTAGG[A/G]CACGCAACGGGTTTC | 6045 |
rs562242376 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063294 | TGGCTGGCTTTTAAA[C/G]TGGGGGTGGATGAGG | 6045 |
rs562335787 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045498 | CCCCTCAGTCTCTCA[A/T]GAATATTGAGCGGCC | 6045 |
rs562351035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076429 | CCAAGTAGCTGGGAC[C/T]ACAGGCGCGTGCCTC | 6045 |
rs562361529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088834 | CAAGTGAGGTGCTGT[A/G]TGGGCATTGTATTAA | 6045 |
rs562363481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096909 | GTTATTTCTTTGTTC[C/T]GGCAGTAAACATAAT | 6045 |
rs562437077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070857 | TAGCCGGGATGGTCT[C/T]GATTTCCTGACCTCG | 6045 |
rs562473132 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185077068 | AAATTTTGTTGCTAT[C/T]GTGAATGGGATCTTT | 6045 |
rs562502918 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043853 | GAGACGCAGTCTCGC[C/G]GAGACACCCAGGCTG | 6045 |
rs562550864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071253 | TTATCCTTGTCTTCT[A/G]CCTGTGAAGATAAGC | 6045 |
rs562554123 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063883 | CAGCTTCTTTGACTC[C/T]GCTTCTCACATCACA | 6045 |
rs562589566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049235 | AAAAATCAGGATCTC[A/G]TGCCACACTATCAGA | 6045 |
rs562589577 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079579 | CCTCTCCTCTCATTG[A/G]AACAGTCATTTTATT | 6045 |
rs562634060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185082314 | GGTCACTATGCTCCG[C/T]GTCTTCAAGGTTCTT | 6045 |
rs562663819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049786 | CAGCATTGTGTGCTT[A/G]CTGCTAGTACTTATA | 6045 |
rs562665938 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044506 | ACCTAGGATTCAATA[C/T]AATTCTCTCATCTCG | 6045 |
rs562697012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185052727 | AATGAGGTGACCATC[A/G]TTTTAGGTGAGCTGA | 6045 |
rs562759829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099219 | CACCTGGCTAATTTT[G/T]GTATTTTTAGTAGAA | 6045 |
rs562775006 | in-del | -/ATGTT | 0.00716266 | 0.059414 | intron-variant | RNF2 | GRCh38.p7 | 1:185072238 | AATATCTGGACTCTC[-/ATGTT]GAGGGGTTTTTGGTT | 6045 |
rs562831285 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088729 | AAGCAACCACAACTG[-/A]AAAAAATCCAGGAAG | 6045 |
rs562906822 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046899 | TGAATATTCTAATAA[C/G]TGAGGTGGGTGTGAG | 6045 |
rs562911504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058002 | TGGTGGTGCACACCT[A/G]TAGTCTCAGTTACTC | 6045 |
rs562946381 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071621 | CCATGCTAGATTCAG[A/C]CCCACCTCCCCGCCA | 6045 |
rs562948978 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065110 | CAGTCAGCACTCTGT[A/G]AAAACGCACCAATCA | 6045 |
rs563004558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084246 | TGTTGGCTTTAATTG[C/T]TAGCTCAGCCTTAAA | 6045 |
rs563024439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051305 | GAAGGGGTAGTATTG[C/T]GTATAGTAGGAGTTG | 6045 |
rs563042101 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185065028 | GAGAGATGAAGCCAG[C/G]TGGACTTCTGGGTCG | 6045 |
rs563153328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098645 | TGGCAAGAATGGCTA[C/T]GTTACCACTGTATCT | 6045 |
rs563179650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058372 | AGGACTGTACTCTGT[A/T]ATTTTGTGTGCATGT | 6045 |
rs563180438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054790 | GCATCCTCCGCCTGC[C/T]GGGGTCAAGCGATCT | 6045 |
rs563224417 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090956 | TATATTCTGGTTTAA[A/G]TCAGCTCCTGGGTTA | 6045 |
rs563315376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063177 | TATTTGGGGAAGTAC[A/C]ATTTGGAAATGCCAG | 6045 |
rs563327533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087694 | TGTAAACTGGGATAC[A/G]TTTTTAGAACATGAA | 6045 |
rs563348494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069866 | TAACAGTTGACAACT[A/G]ATAAAGAAATCTGCC | 6045 |
rs563395411 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102551 | AAACTTTTTCATCAC[C/T]CCAAACAGAAACTCT | 6045 |
rs563399706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096417 | TTTCATCTTATAAAA[C/T]TGAAACCCTGTATCC | 6045 |
rs563405030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087101 | CCAGTGAATAATTTG[G/T]TTTTTTTATTCTCAA | 6045 |
rs563417567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185061277 | GGACTACAGGCGCCC[A/G]CCACCATGCCCGGCT | 6045 |
rs563444305 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185068056 | TTGCCCACGCTGGAG[G/T]GCAATGGTACGATCT | 6045 |
rs563467697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060685 | TAAATTGGATGAATC[A/G]GTAGACTGGAAACCC | 6045 |
rs563483505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067525 | AGAGAGTTAATTTGA[C/T]GTGACCTTTATTTTA | 6045 |
rs563614989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185056201 | AAGATAATATTACAG[C/T]TGTGTATAGTGTAGA | 6045 |
rs563804944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185099672 | GATATTATTTTGTCA[A/G]TAATTGAGACATTGC | 6045 |
rs563836438 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092392 | GTGTTGGTCAGGCTG[G/T]TCTTGAACTCCTGAC | 6045 |
rs563858864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074947 | GTCCTGGAACCAATC[C/T]CCCTTGGATACTGAG | 6045 |
rs563973151 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088368 | CTAAAGGAAGCCTTA[C/T]CAACATGGAGAAACC | 6045 |
rs564003874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075383 | ATACATTCCTTATGC[A/G]AAATACTGTAATTAT | 6045 |
rs564035358 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071688 | GATAGATTTCACCTG[C/G]TCATTCAGGTAATGC | 6045 |
rs564067880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077817 | TTTCTAATGCCTGAT[G/T]CATTGTTTTTTTTCA | 6045 |
rs564170002 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098464 | GATTGCAGGGGTTCA[C/G]TTACTAGCTGCCTAG | 6045 |
rs564194967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059291 | AAGAAAATCTACCTA[A/T]GTGACGGGGGACACA | 6045 |
rs564215876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078472 | GTTATTCCTTGGTTT[C/G]CCTATCTTACATGGC | 6045 |
rs564319689 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185092267 | CTGCAACCTCCACCT[A/C]CCGGGTTCAAGTGAT | 6045 |
rs564320285 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060086 | TTTCTCTACCCAGGA[A/C]AGGATAACAATCTTG | 6045 |
rs564322365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185084140 | GAGGAGATGGCTTCT[G/T]GCTATGTTGCCCAGA | 6045 |
rs564406345 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069662 | ACAGCAGTGTGCCTA[A/G]CCTATAATATCTTAA | 6045 |
rs564453423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079799 | CCAGGTGTGGTGCTG[A/G]GCGCCTTGTAGTCCC | 6045 |
rs564481409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093328 | TTCTGAATACTTTAT[G/T]AACAATTAAATTTAC | 6045 |
rs564500168 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046008 | CTCGCCTCCGGGGGC[-/G]GGGGGCCCCAGCCTC | 6045 |
rs564503315 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185051809 | CACACCAATTTTTAC[-/AT]ATATATATACACACA | 6045 |
rs564522223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079367 | AGAATGGAGTCACTT[A/T]TCCTAAGTGCCACAT | 6045 |
rs564568000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073407 | GGTGAGGATTCAGCT[A/G]AGACAGTAGAGTGAC | 6045 |
rs564573447 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059868 | AAGAGTGTAGAGGTA[G/T]TAGCCTTCAACTTTT | 6045 |
rs564602466 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185072840 | AGCTACTTGGGAGTC[A/T]GAGGCAGGAGAATCG | 6045 |
rs564734956 | in-del | -/CTC | 0.00636936 | 0.0560724 | intron-variant | RNF2 | GRCh38.p7 | 1:185074413 | ATCTTGTGGTTGGTT[-/CTC]CTGAAAACCAGTCCC | 6045 |
rs564742730 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058913 | GTCATGTTGATTTCC[A/G]GTATATATGAAGTGT | 6045 |
rs564743678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081805 | CAGTGCCAGCCGTGG[A/G]CATTGCAGTTTTCGG | 6045 |
rs564874245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096281 | ATAACAGAATTTTCC[A/G]TCTTAACCATTTGTA | 6045 |
rs564956617 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094403 | GCCTCGGCCTCCCAA[A/G]GTGCTGAGATTACAG | 6045 |
rs564962199 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185076197 | GAGGCGAAATATGAA[C/G]CTTTCAGTCTTCTGG | 6045 |
rs564984640 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185088788 | AAATTTGAATTTTCC[A/G]TGTGCTAATAAGTAC | 6045 |
rs564992451 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072960 | AACAAACAAAAAAAC[A/G]TAGTGAACAGAACTC | 6045 |
rs565019728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082270 | TTCTATGATTGTCCT[C/G]AGTTGGTCGTTGTCA | 6045 |
rs565032874 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048240 | ACTATAGGTGCTAAG[A/T]GCGTAGGTGTGACCC | 6045 |
rs565061083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051870 | TATACATGCATATAT[A/G]TATGTAAAAATGTGT | 6045 |
rs565127385 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062931 | TATCAGATTGGGCAG[G/T]GTTTTTTAAAAAAAT | 6045 |
rs565165523 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085659 | TCTCCTGTTTAAAAC[-/T]TTTTTTTTTTTTGAG | 6045 |
rs565173806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074966 | TTGGATACTGAGGGA[C/T]GACTATATATAGTTC | 6045 |
rs565188227 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083267 | CGAAGGATTGTATGT[A/T]TGTTTTAGTTCGTAT | 6045 |
rs565279791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090518 | AGGCTGAAATCTAAC[A/C]AACATTTTATTAATG | 6045 |
rs565336075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091106 | AATCTTGTTTTAATG[A/G]GCAGCATGAAACATA | 6045 |
rs565422418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098469 | CAGGGGTTCAGTTAC[C/T]AGCTGCCTAGATTGT | 6045 |
rs565426355 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057193 | GTGCACACCTGTAGT[C/G]CCAGTTACTAGGCAG | 6045 |
rs565547796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058846 | GATATCACTTAAAAC[A/G]TGCTCATTTTATAGA | 6045 |
rs565574340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096021 | TATTCTTTAAACGCT[A/G]CCTGCAGTTACATTA | 6045 |
rs565623366 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185053228 | AAAATCCCCTTCATA[G/T]TCTCCCCACATTCCA | 6045 |
rs565647204 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051476 | ATAAGAAGTAATGTA[C/T]GTAAAGCGGTCTTTG | 6045 |
rs565677866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185085842 | TATTTTTAGTAGAGA[C/T]GGTTTCACCATGTTG | 6045 |
rs565706512 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075500 | GTTCTTGCATTGCTG[C/T]GTAACTCCCTGAGAC | 6045 |
rs565729485 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102164 | GGAGGATATAAACTG[C/T]ATCATTAGTGAAATT | 6045 |
rs565839461 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185045964 | GCTGCCCTTTCCTCT[A/G]CGCGGAGGCCGGCGC | 6045 |
rs565952406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060914 | ACTTGAGGCCAGGAG[C/T]TCAATACCAGCCTGG | 6045 |
rs565992554 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185050073 | TGGAGTTGAGAGACA[A/G]TAAGTAAATGATCTG | 6045 |
rs566036305 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101533 | AGAAATAAGATTGAC[C/T]TGGGTGTTATATTTC | 6045 |
rs566052538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054472 | TGGCAAGCAGGCCTT[C/T]TTCTCCCATCTGGGT | 6045 |
rs566147852 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072891 | GTTGCAGTGAGCCGA[A/G]ATTGTGCCACTGCAC | 6045 |
rs566164812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185054859 | GGCGCCGCCACGCCC[A/G]GCTATTTTTTTTCTA | 6045 |
rs566170598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094835 | TTATTCAGGCCTCAA[A/G]GAGAATCATTATTTT | 6045 |
rs566240666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067780 | CAGTGATGCAATCTC[A/G]GCTCTCGGCAACCTC | 6045 |
rs566306762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064556 | TGAAAACATTGAAAG[G/T]TGAAAACACTTTAAG | 6045 |
rs566352092 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070374 | TTTACTGTGCTTTCT[G/T]ACTGTCTCATTTGTT | 6045 |
rs566444181 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | RNF2 | GRCh38.p7 | 1:185097321 | TTTGTATCGCCTTAG[C/G]TGACTTGGCGGAAGG | 6045 |
rs566580745 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066522 | CTGCTTATTTATGCC[G/T]TCTTAGCATTTATCA | 6045 |
rs566596258 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092854 | ATTTTTTCTTTCGAC[A/G]AGTGGTATAGAGGGT | 6045 |
rs566689802 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070642 | TATTTTCTTTTCTTT[C/T]TTTTTTTTTTTTTTG | 6045 |
rs566743843 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095803 | TTCTACTTCTGTGTT[C/T]ACAAATATTTTTATG | 6045 |
rs566851741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072270 | GTTATTTTTTTAGGC[A/C]TGAAAATGTGAAATG | 6045 |
rs567060068 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061288 | GCCCGCCACCATGCC[C/T]GGCTAATTTTTTGTA | 6045 |
rs567069423 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043914 | AACCTCTGCTTCCCA[C/G]GTTCAAGCGATTCTC | 6045 |
rs567082424 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096314 | TGTAGAGTTCAGTAG[C/T]GTTAAGTACATTCTT | 6045 |
rs567091916 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185091424 | GCTGTAGGCGATTAT[A/C]GTTGAAACAAAATTA | 6045 |
rs567109336 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051399 | TTTCTGAGTCTCTTT[A/T]CTTTTGTTAAAAAAA | 6045 |
rs567160487 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044627 | TCCCACTGCAGTCCA[C/T]TGGTTTATGCCTCTA | 6045 |
rs567170952 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099471 | ATTAGGGTTTGGGGG[G/T]TATGTTCCTTTTTTT | 6045 |
rs567172962 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068427 | GATTATCCAGGTAGG[A/C]CTTAAATGTTACCAC | 6045 |
rs567210704 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083525 | TCCTTCCCACTCAGG[G/T]TCTCTCCTGCAGCCT | 6045 |
rs567238072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185068592 | GGTAAGGAACAGATT[C/T]TCCCCTAGGGCCTCT | 6045 |
rs567297901 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185088150 | ACTAAATACAAAATT[G/T]TAGGGATTGACAGCA | 6045 |
rs567335481 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094603 | TTTTCTACTTCCCAT[G/T]CTTACTCCCACATAG | 6045 |
rs567344388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074988 | ATATAGTTCCGTGTG[G/T]GTGTGTGTGTTATTT | 6045 |
rs567391067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185054462 | CTTGCAATACTGGCA[A/G]GCAGGCCTTCTTCTC | 6045 |
rs567483846 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185062580 | AGGTGGTTGTTTTTT[A/T]TAATTTTAGAGTATG | 6045 |
rs567497050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185045974 | CCTCTGCGCGGAGGC[C/T]GGCGCTGCGGCGCGG | 6045 |
rs567522703 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185061610 | AGTGGGAAAAAAACG[G/T]CAGGAATCATTAGCT | 6045 |
rs567596156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048511 | TAAAAATCAGTTTAT[C/T]TGTATTAAGTACAAT | 6045 |
rs567596541 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185055682 | TGCCTTGGCCTTCCG[A/C]AGTCTGGGATTACGA | 6045 |
rs567597483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095207 | GTTCAGTTTAGCCTT[C/T]TACTAAAAGCAAGAC | 6045 |
rs567607334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049279 | GGGACCACTGGGGAA[C/T]AGCAGAACATTTACT | 6045 |
rs567614444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086491 | GAATTAATCAGCGTG[A/G]TGAGGAGACTTTGAA | 6045 |
rs567628624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096461 | TCCTCATTTCTCCCT[C/T]CCCCCAGTTCCCGGT | 6045 |
rs567759687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059464 | AGAACATAACTTTTA[C/G]GTAGCTGTCCTTGTA | 6045 |
rs567776586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085412 | AAGTGCTGAGATTAC[A/G]AGCGTGAGCCACCGC | 6045 |
rs567785547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089166 | CATGTGCAGTTCTCA[A/G]TAGGGTTCGGACTCT | 6045 |
rs567828742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185095955 | TGTAGTATTATAGAC[A/G]TGATTTGATAAATGT | 6045 |
rs567836617 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103011 | CGTTCTGGCTTTTCC[A/G]TATCCTCTGTAACAC | 6045 |
rs567880428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185065317 | CTGTAAAATGGACCA[A/G]TCAGTAGGATGTGGG | 6045 |
rs567882313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058113 | CATTGCTGACAGAGC[A/G]ATACCCCATCTCAGA | 6045 |
rs567919137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053174 | TTATCTCATTTAATC[C/T]TTTATTAAGGAAGGT | 6045 |
rs567919491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064730 | ATGGGATGTCTTTCC[A/G]TTTATTTATGTCTGT | 6045 |
rs568077247 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044849 | TTAATCTATTACTTC[A/G]TAAATCCTCAAGTTC | 6045 |
rs568111439 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089583 | TGAATCAAGGATATG[A/G]TAATTATATATATAT | 6045 |
rs568158410 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100313 | ATGAGCCTTTAAAAA[C/T]CAATTCTGAGACTGA | 6045 |
rs568334158 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055693 | TCCGAAGTCTGGGAT[G/T]ACGAGGTGTGAGCCG | 6045 |
rs568338814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085789 | CTCCCGCATAGCTGG[C/G]ATTACAGACGCGCAC | 6045 |
rs568364596 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079478 | CCTGTTTTAACCTTT[C/T]AAAGGAAAGCATCTT | 6045 |
rs568427736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060286 | ACAGATAACTGATCT[A/G]TATCATTAAGTCTAC | 6045 |
rs568449767 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057979 | AAAATACAAAAATTA[A/G]CCGGGCTTGGTGGTG | 6045 |
rs568466598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067121 | GATACAATCAAATTA[A/G]GAATTGATATTGCTT | 6045 |
rs568506709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093696 | CATTTGACACAATTA[A/G]TTTCTCCCTTCTCTT | 6045 |
rs568510983 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185093937 | TACCATCTGTATGCT[G/T]ATGACTCCCAAATTT | 6045 |
rs568543723 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101060 | AGTCTTCAAGTATAC[A/G]TTTGAGAGTGCTTTT | 6045 |
rs568546309 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185060845 | GGAAACAGGCTGGGC[A/G]AGGTGGCCCACACCT | 6045 |
rs568650058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185072905 | AGATTGTGCCACTGC[A/G]CTCCAGTCTGGGCAA | 6045 |
rs568661486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185078819 | GGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTC | 6045 |
rs568760346 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185066302 | CTGAGGCTGTACTCC[C/T]CACCTTCTTTTCCAC | 6045 |
rs568833031 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185096562 | TTTGTACTTTTGGGG[G/T]TTTTTTTTTGTTGTT | 6045 |
rs568872331 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065328 | ACCAATCAGTAGGAT[A/G]TGGGCAGGGCCAAAT | 6045 |
rs568876224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070544 | GATCTCAAAGAGTTG[A/G]ATGGGAACCTCAATT | 6045 |
rs569031595 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185051881 | ATATATATGTAAAAA[-/TG]TGTGTATGTAAAAAG | 6045 |
rs569085548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075113 | CATTCTCCTGCCTTA[C/G]CCTCCCTAGTAGCTG | 6045 |
rs569110574 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055944 | CTGTGGGGTGCTATC[C/T]TCTAGTAACATTTCC | 6045 |
rs569125706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075731 | AGAACTCATTAACAC[A/G]AGAACAGCAAGGGGG | 6045 |
rs569164205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081854 | GCATATTTCTCAGAT[A/G]TAATGGTTTTGCTGG | 6045 |
rs569294809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083484 | CAATTTCTCATGTCT[C/T]TCCCCTCCACTCTTC | 6045 |
rs569325213 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071436 | GGCTACATATGTCTT[G/T]GTTGTGAAATTACAG | 6045 |
rs569329788 | in-del | -/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100902 | CATTGTCATGCAATG[-/T]TTTTTTTTTTTCCAT | 6045 |
rs569361666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185046373 | TTCGCGTTTTGAACC[A/G]TGTCGTTTACGCTGA | 6045 |
rs569367552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185077343 | ATTTTTTTTCCTACC[A/G]TAACATGACGTAGGA | 6045 |
rs569385399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050182 | TTCTGTATGCCAGAC[C/G]CTGTGCAAGGGATTA | 6045 |
rs569475720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185057304 | CAACCCTGTTTCAAA[A/C]AATAAATAAATAAAT | 6045 |
rs569530245 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185090598 | GAGTAATCCATCTTT[G/T]ACCATATAAAGAAAG | 6045 |
rs569532449 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF2 | GRCh38.p7 | 1:185082695 | ACTGCCCTGTACGTT[C/T]GTTAGCAGTTCCTGG | 6045 |
rs569570589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086458 | CTCTTCAGTTCATTT[A/G]TATCGGGAAAGGAGG | 6045 |
rs569620172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090022 | TACCTCCCAGATTCA[A/T]ATGATTCTCCTGCTT | 6045 |
rs569672766 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079964 | TGTGTCTTTAAACTT[A/G]TTATAATTTTGTCTT | 6045 |
rs569681824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185080136 | TTGCTGGCTTCCACT[C/T]TACTCTTCAGCTTTT | 6045 |
rs569697452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095357 | ACCAAGCATGCTTCT[G/T]CCTCAGAGCCTTTGT | 6045 |
rs569772832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087995 | TAAGGCACCAAGGAA[A/G]ACTGTTTTGAGATGA | 6045 |
rs569809674 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185056612 | CTGGCCTCAAGTGAT[C/G]CTCCCTCCTTGGCCT | 6045 |
rs569841181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053288 | TTTATGTTGATCCAC[A/G]TACTCCTGTCATTAT | 6045 |
rs569841521 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053101 | TGAACCTAGGCAAGT[C/T]AGGCTCTAGACATTG | 6045 |
rs569848885 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100889 | ATGAACTTAGTGTCC[A/G]TTGTCATGCAATGTT | 6045 |
rs569888210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085861 | TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAACT | 6045 |
rs569923529 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185094515 | TATTTTTTGCTTTCT[C/G]CATAGTATATCCAGA | 6045 |
rs569959530 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185054890 | TTTTTGGTGGAGACA[A/G]GGTTTCTCCATGTTG | 6045 |
rs570012544 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185093607 | CCCCATCATATTGCT[C/G]TTATCAATGTTATTA | 6045 |
rs570046816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068495 | AGCCACAGAAGAGCA[A/T]GAAGCAGTGTGACCA | 6045 |
rs570067894 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076222 | TTCTGGGTATTGTAT[C/T]TTGCTTTTAGGCTGC | 6045 |
rs570151055 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077967 | GGACAAGTAAGGGGC[C/T]GGGCGTGGTGGCTCA | 6045 |
rs570152875 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050132 | ATTTAAATAGGGAAT[C/T]CTGTGTTAACGTTGC | 6045 |
rs570179831 | snp | A/T | 0.000115791 | 0.00760804 | intron-variant | RNF2 | GRCh38.p7 | 1:185091753 | GGGTATGTTGAAAAG[A/T]GTTGTTATACTAGGT | 6045 |
rs570181509 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083090 | TTTGGATAGGCTCTG[G/T]CCATTGTTTTTTTCC | 6045 |
rs570222443 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102867 | GTTCTGCCTTCTGTT[A/G]TTTTGGGTATATATG | 6045 |
rs570248874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185061494 | GCACCAAGGCCAACA[A/G]TATAGAGGAAAACGA | 6045 |
rs570250303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074340 | CTTTTCCCTCTTTAG[C/T]GGTAGGGGTAGGATG | 6045 |
rs570257717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090704 | TTCCTTTACAATTCT[C/T]GCCATACTAGAACTC | 6045 |
rs570259400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098814 | TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG | 6045 |
rs570329472 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077250 | ATTATTTGCACTGAT[A/T]CTTTGATCACTTCCT | 6045 |
rs570333665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070958 | CAGTATTTTTATTCC[C/G]TCAACTAACTTAAGG | 6045 |
rs570434104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185058083 | GTGAGCCTTGATTGC[A/G]CCTTTGCATTCCAGC | 6045 |
rs570436906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185086139 | TTCATCTCTACCAAA[A/G]CCTCCTTAACTCCTC | 6045 |
rs570445750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071381 | CCATCTTGGGAGATA[C/G]GTGACCCTCTATTGT | 6045 |
rs570546368 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057792 | ACTGCAGGTGGAAAA[C/T]TACTCTAAAGGGGAA | 6045 |
rs570548986 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043468 | CTTTTTAATCACATT[C/T]AATCCAGATATCCCA | 6045 |
rs570688879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185064179 | TCATATTCTAGCCCT[A/G]AATAAATTAGCTTCT | 6045 |
rs570722974 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078676 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC | 6045 |
rs570782327 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043483 | TAATCCAGATATCCC[A/G]TAAGTTTTCCGTTTT | 6045 |
rs570879287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072395 | GTACAGTGCAAGGTA[C/T]TGGGGATATTGTGGT | 6045 |
rs570888917 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050495 | TAATTATTATTTTGT[A/G]TTTCTCTGTGCTTTA | 6045 |
rs570921673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059597 | TTGCAGCAGACATCT[C/T]CATGTTAATGGCATT | 6045 |
rs570954594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185081905 | ATCAGAAAGCTGTAG[C/T]GGCAGCAGACCACCA | 6045 |
rs571100514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185085358 | TTTCACCGTGGTCTC[A/G]ATCTCCTGACTTCAT | 6045 |
rs571101592 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044003 | TTTTTTTTGTATTTT[C/T]AGTAAAGACAGTTTC | 6045 |
rs571167050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078177 | GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA | 6045 |
rs571200133 | in-del | -/GGCAGAAGAACCCA | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045207 | GTGGGCCGAAGCCAG[-/GGCAGAAGAACCCA]GGCAGAAGAACCCAA | 6045 |
rs571332387 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185087325 | CTCTGTGTCAGAACA[G/T]GCTGGAAGGGCCAAA | 6045 |
rs571358364 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072480 | AAGAAAAGAGAGAAC[A/G]TGAGATAAAGAATTA | 6045 |
rs571363050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070257 | TATCACTTTGCAGAT[C/T]AAAAAAAAGCCTTAA | 6045 |
rs571400853 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185069472 | AAAAAAAAAAAAAAA[A/G]AAAGAAATGCAGAAC | 6045 |
rs571421923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049024 | CGAGGTCAAGTGTTC[A/G]AGACCAGTCTGACCA | 6045 |
rs571474010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081341 | GTGGTAGTTGGTTGG[C/T]GAGAGGTCCGATGAC | 6045 |
rs571512664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047169 | TGTAGTTATTTTCCT[C/T]AGGTATCCTTGTGGC | 6045 |
rs571526668 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185074466 | GCCCACCTAGAGTAA[A/C]CATATTAGCATAAAC | 6045 |
rs571530174 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185082001 | TGCTTCAGTCCAACC[A/C]CTGAGCGGGTCGTCA | 6045 |
rs571562321 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067979 | CTTCCAAAGTGCTGG[C/G]ATTACAGGCATGAGC | 6045 |
rs571594521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185089990 | GCAGTGGCGTGATCG[C/T]GGCTCACTGCAACCT | 6045 |
rs571608352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185080890 | AGGGTAGCGTTCAGT[A/G]GGCAGAAGGAGTGTT | 6045 |
rs571685985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185078371 | GCTTCTCTTTAGCTC[C/T]GTAACCTCTTCTTGT | 6045 |
rs571756185 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185082638 | GGGGTTACAGGCGTG[A/G]GCCACCGCACCCAGC | 6045 |
rs571823601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063346 | AGTCTGAAATGCAAC[C/G]TTGGTATCAGAATTG | 6045 |
rs571848930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185078942 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 6045 |
rs571856748 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | RNF2 | GRCh38.p7 | 1:185072064 | GGGGTTGCTGTCATC[A/T]TGGGAGGTGGCTAAG | 6045 |
rs571863435 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | RNF2 | GRCh38.p7 | 1:185077815 | ATTTCTAATGCCTGA[-/T]TTCATTGTTTTTTTT | 6045 |
rs571881585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052518 | TATCCAGAATAGAAA[A/C]ATCCATAGATTGGTG | 6045 |
rs571920733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051825 | ATATATATACACACA[C/T]TTTATGTATATATGT | 6045 |
rs571975380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096520 | TTGACTTCTTTAGAT[A/C]CCTCACATAAGTGAA | 6045 |
rs571980187 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044455 | TTATTTGGAATTGCT[C/T]ATAGAGAGTTTCAGA | 6045 |
rs572176405 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043624 | AATCTAACCACACAT[C/T]ATGATTTTCAAAGGC | 6045 |
rs572198978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091035 | TTTCGGGGTTCAAAA[C/G]TATTTTAAAATGAAA | 6045 |
rs572231841 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044253 | AAAAAGAATAATGCT[G/T]GTTTTCTTTGATGGA | 6045 |
rs572256451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185091893 | CGATCTTGGCTCACT[A/G]CAACCTCTGCCTCCT | 6045 |
rs572262429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185099045 | CCAAGCCACTGTGCC[C/T]GGCCTCTTTTTTTTT | 6045 |
rs572339948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185093917 | CTCAGTTTCATAGTT[C/T]TATTTACCATCTGTA | 6045 |
rs572366061 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185069430 | TCACTGCACTTCAGC[A/C]AGGGTGATAAGAGTG | 6045 |
rs572394564 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071198 | GAAAAAGTCAGTTAC[A/G]CATTCATCTCAGGGT | 6045 |
rs572420711 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100364 | TTTAATATTAAAGAT[A/G]TACTGGCATTACTTT | 6045 |
rs572433818 | snp | A/G | 1.65143e-05 | 0.00287348 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093085 | ATGTCCTACCTGTCG[A/G]AAAAAACTAGTTTCC | 6045 |
rs572478222 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045189 | GGCCAGGAAGGTGTA[A/T]AGGGTGGGCCGAAGC | 6045 |
rs572540984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185079771 | CCGTCTCTACTAAAA[A/G]TACAAAAATTAGCCA | 6045 |
rs572575068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185066365 | GACATGCCATGCTGA[A/G]TGTACCTTTCCTTAT | 6045 |
rs572687127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185059803 | TATTTTTATCTCTAG[A/G]AATGAATTCCTTAGC | 6045 |
rs572698617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185060396 | CACCACATAAGTATA[C/T]TCCCTTGTTTAGAGG | 6045 |
rs572715781 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094956 | CATGGCTTTAGGCAT[C/T]ATCCCGGTCCCAGTA | 6045 |
rs572776790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053506 | TGCACTAATATTCTT[A/G]TTTTCTTTCTTTCTT | 6045 |
rs572779920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185096262 | AAATTGTGGTAAAAG[A/C]CATATAACAGAATTT | 6045 |
rs572801176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185097612 | CATCCTAGTTTACTG[C/T]GCCCTTCAACTCCTG | 6045 |
rs572814985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185090062 | AAGTAGCTGGGATTA[C/T]AGGCGTGTGCCACCA | 6045 |
rs572878934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185056670 | GCCACTGCACCTGGC[C/T]TATCATTCATTTCTT | 6045 |
rs572939791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185082149 | CTCATGAGACACCCA[C/T]TTATCGAGCTTTTTC | 6045 |
rs572949545 | in-del | -/TTTCCC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090255 | TTACACCAAGGTGGT[-/TTTCCC]TTTTTCTTTTCCCCT | 6045 |
rs573040230 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062997 | TATAATAATTTAGCA[A/G]TATTTGTCAGAATAA | 6045 |
rs573096650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185062277 | TGAATCAGGCAATCA[C/T]TTATTGTTGACAGTG | 6045 |
rs573116910 | in-del | -/GTTAAAA | 0.00159617 | 0.0282053 | intron-variant | RNF2 | GRCh38.p7 | 1:185051405 | AGTCTCTTTTCTTTT[-/GTTAAAA]AAAATAAAAAATGCC | 6045 |
rs573153731 | in-del | -/A | 0.0832709 | 0.186283 | intron-variant | RNF2 | GRCh38.p7 | 1:185053889 | TTAATGTCTTGTATT[-/A]AAAAAAAAAAGTCAC | 6045 |
rs573171504 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056003 | TTAAAGGCTCTCAAA[A/G/T]ATTAAAGTACTATCT | 6045 |
rs573180523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071522 | AACTTCCCCTTTGGC[A/G]TCGTGCGTTTAGAGT | 6045 |
rs573211754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064442 | ATTTACAGTGGTTCG[A/G]CTTACGATTTTTCAA | 6045 |
rs573276220 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088037 | GGGAGGAGCAGGTTT[A/G]AAGGCAACAAACATG | 6045 |
rs573392417 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF2 | GRCh38.p7 | 1:185061130 | TATTTCTCTCTCTCT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs573452485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185076098 | TACATATGTTGCACA[C/T]ATTTTTTTCCTAGCT | 6045 |
rs573452570 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185082822 | TAACATTTCCATAGT[A/C]TAAAATAAACATAAA | 6045 |
rs573465950 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066360 | TCCCAGACATGCCAT[C/G]CTGAGTGTACCTTTC | 6045 |
rs573569713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185067403 | AATTTCTAAAATATA[A/G]CACCTGTATCCTGTA | 6045 |
rs573673792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185081037 | TCTGAAAGATCTATC[C/T]AGGATATATGTTAGA | 6045 |
rs573737201 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090789 | TCACTGCCAGCTTGT[-/G]GGAGAGGGTAGTGAA | 6045 |
rs573757559 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064653 | TTGGGATGTAACCCC[A/G]TGTAGGTCAACGAGC | 6045 |
rs573773455 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093743 | CCTGGCTTTCAGGAG[A/G]CCATAGTCTCTTGGT | 6045 |
rs573803587 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185073197 | AGATTTTTATGGGTT[A/C/T]TTTGCTACTACAAAT | 6045 |
rs573834750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081498 | TCCTGGGTTCAAGTG[A/G]TTATCCTGCCTCAGC | 6045 |
rs573895721 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068948 | TTAGGTGCAGAACTC[C/T]TGACAGTTTTGCTCA | 6045 |
rs573897932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185054677 | TTCTTTTTAATCTTT[C/T]TTTGTGGGTTTTTTA | 6045 |
rs573959009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185087488 | TTGGTGGGACACATA[C/T]ATTCAGACCATAGCA | 6045 |
rs573997434 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185086912 | ATATTTATTGTTTTG[A/G]GTTAAGACAATCTTG | 6045 |
rs574041842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185075161 | ACCACACCTGGCTAA[C/T]TTTTTTATTTTTAGT | 6045 |
rs574080094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083887 | GCTGGGATTACAGGT[A/G]TGAGCCACTGTGCCT | 6045 |
rs574118294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046717 | CGCTGTTTTTCAATT[A/T]AAAAAATTAAGGCAT | 6045 |
rs574255418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185047629 | AAAGAAGCATAATTT[C/T]TTCCAGCAAGAGAAA | 6045 |
rs574276076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095417 | TTCCAAATAATCCAC[A/G]TGGCACACTACCTCA | 6045 |
rs574312554 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056615 | GCCTCAAGTGATCCT[C/G]CCTCCTTGGCCTCCC | 6045 |
rs574402463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185090227 | GCCTGGCCGAGGCTG[A/G]TGAAATTTTTAGTTA | 6045 |
rs574425770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071633 | CAGACCCACCTCCCC[A/G]CCAATCTTGGACAAG | 6045 |
rs574427728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185096223 | TTGTCCCATTATTTT[A/G]GCCCGTTCATACCTT | 6045 |
rs574444823 | in-del | -/TTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087100 | CCAGTGAATAATTTG[-/TTT]TTTTTTTTATTCTCA | 6045 |
rs574544621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185050808 | CTTTCAGAGCCAGCA[A/G]TTTTGACAGGCATTC | 6045 |
rs574625211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051675 | AGTTGTGGATGTCCT[A/G]TAACCCTACTTGTCA | 6045 |
rs574705810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185053420 | AGCTCACTGCAGTCT[C/T]CAACTTTGGGCTCAA | 6045 |
rs574725634 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080587 | AGCATCCATGTGGTA[C/G]TATTTAAGACTGTAG | 6045 |
rs574773929 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084503 | GAGGGGTTTTGTTTC[C/T]CCCTTCTTACTTTTG | 6045 |
rs574777791 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RNF2 | GRCh38.p7 | 1:185052768 | TGAGGCATAGGCTCC[G/T]TGAATTTTTAAGCTG | 6045 |
rs574819188 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045106 | CCTGATGAGGATTTC[C/G]GCCGGGTGGGACAGG | 6045 |
rs574839080 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF2 | GRCh38.p7 | 1:185092582 | GCTGATTTTTAGACA[A/C]TTCATAAGATGAGTA | 6045 |
rs574898250 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076984 | GTTCAGATCCTCTTT[A/T]ATATACTTCAGTTAA | 6045 |
rs574937924 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047941 | AGTAACTTAGTGTTT[A/G]TTTGCATTTAATACT | 6045 |
rs574980365 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051091 | TGTTCTGCTTGTTTC[C/T]CACACCATTCACACA | 6045 |
rs575028932 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185084300 | TGGCTTACCACTCGA[A/G]TCAGCATTGTAGCAA | 6045 |
rs575062194 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053995 | CTGTTAATCTACATT[-/C]CCCCCCCCACCCAGT | 6045 |
rs575114139 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185065536 | TCCTGAAGTCAGCCA[G/T]ACCATGAACCCACCA | 6045 |
rs575138009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185055333 | ATCATGTCCATGTCC[A/G]AAAAGTTTTAGATTT | 6045 |
rs575252579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070732 | CAAGTTCCGCCTCCC[A/G]GGTTCACACCATTCT | 6045 |
rs575275210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048819 | CAGAACAACATACCA[A/G]TAAGTTCAGCTAAGC | 6045 |
rs575309107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185095518 | CCTCATTTTTTTCCC[A/G]TAGCACGTATCACTC | 6045 |
rs575359808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185063684 | GAGTCTTACGGGATT[G/T]AAATTAAGGTGTTGG | 6045 |
rs575385920 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF2 | GRCh38.p7 | 1:185088512 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 6045 |
rs575398523 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054189 | CCACTCCTGGTAGAG[C/G]TGCTAGGGCACGCAA | 6045 |
rs575412071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185074629 | AAAGACCAGATACAG[G/T]CTGCCTTCCTGTATC | 6045 |
rs575438528 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087464 | AGATTAGATTTCAAC[A/G]TAGGAATTTTGGTGG | 6045 |
rs575443081 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | RNF2 | GRCh38.p7 | 1:185064387 | GATTTCATACTCTGA[-/T]TTTTTTTGGTAATGC | 6045 |
rs575526543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185068078 | GTACGATCTCGGCTC[A/G]CTGCAACCTCTGCCT | 6045 |
rs575603920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185062102 | TACAAACATGGAAGA[A/G]AACTGCTAGGGAGAA | 6045 |
rs575648315 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185072588 | AAGCAGAAGGACTAG[C/G]TAGTGGAAGGACTCT | 6045 |
rs575670728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185077162 | TTTTTTATCTTCATT[A/C]CACCATGTTACTGCT | 6045 |
rs575709782 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051877 | GCATATATATATGTA[A/G]AAATGTGTGTATGTA | 6045 |
rs575761794 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185073130 | AGTGTTTATAGCTAC[A/G]TAGTATTCTATACTA | 6045 |
rs575806776 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045023 | TATCCTGCAAGGATG[A/T]AAAGTGTATGTTTGT | 6045 |
rs575841792 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044454 | TTTATTTGGAATTGC[C/T]TATAGAGAGTTTCAG | 6045 |
rs575847245 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058622 | TGAGTTTTGCTTTTG[A/G]GAGAATGGATTTTGC | 6045 |
rs575847289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185076001 | GTATTGTGTTAATTA[C/T]TCATCATTTTGCTTA | 6045 |
rs575893113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089406 | CTTGAGCATCCAAGG[A/G]TTTTGATATCTGTGG | 6045 |
rs576014503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185086784 | GACTAGTGGTTTAAA[A/G]TGCTCTAAAGTAGAT | 6045 |
rs576074706 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086613 | TTTGAAAGGCTGTCA[G/T]GTAGAAAAATTATAG | 6045 |
rs576111503 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071540 | GTGCGTTTAGAGTCC[C/T]GAGATTCTATTTTCT | 6045 |
rs576169698 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF2 | GRCh38.p7 | 1:185085150 | CTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs576216155 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185079003 | CCCTAAAAGATCATT[C/G]TGAATATCTTATTGA | 6045 |
rs576286284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185092530 | AATCTTTCTAAAGCC[A/T]AAGTTTTAATTGTAG | 6045 |
rs576302699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094934 | CACTCAGAAAACTTT[C/G]AAATCTCATGGCTTT | 6045 |
rs576341322 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185094135 | CTTTGGAGTCAGTTT[A/T]TTTTTTTTATTTTTT | 6045 |
rs576414533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185090153 | TCTCGAACTTCTGAC[C/G]TTGTGATCCACCCGC | 6045 |
rs576546112 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185046591 | ATCTTTTTCGAGGCT[G/T]TCGGAAGTTTTAGAG | 6045 |
rs576560161 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101489 | ACAATATTGGGTGTT[C/T]GGGAGCCAGAAAGCT | 6045 |
rs576686806 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102290 | GGGAGAGGCGATGCT[A/G]TTGGCCATCACTACC | 6045 |
rs576697610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185097376 | TTCTTCTTAACTTTT[A/G]TTTCCTTAAGAATTT | 6045 |
rs576734302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF2 | GRCh38.p7 | 1:185096806 | TACTCTCTTGGTTTT[A/G]CAATGATCTATGAAT | 6045 |
rs576786701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046148 | ACTTTGTGCAGATAT[C/T]GCTCCTTCCTTCTGG | 6045 |
rs576791858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185051886 | TATGTAAAAATGTGT[A/G]TATGTAAAAAGTCGT | 6045 |
rs576821449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185083752 | CTGGGACTCCAGGTG[G/T]GTGCCACCACTCCTG | 6045 |
rs576854262 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056042 | AAATCTAAATTTCTT[C/T]ATTCTTAATGTTAGA | 6045 |
rs576910952 | snp | A/C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094448 | ACCTGGCCTTGGAGT[A/C/T]GCTTTTAAATCTCTT | 6045 |
rs576916186 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185050677 | TAGAAAATAGTTTGG[G/T]TAAAGTGTTACTTGA | 6045 |
rs577032061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185089702 | GCAAAAACTGGAGAC[C/G]AATGTGAAATTGAGT | 6045 |
rs577057806 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | RNF2 | GRCh38.p7 | 1:185057504 | TTATTCATGTGGCGG[G/T]GGGATGGAAGTAAAG | 6045 |
rs577101471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185056987 | TAGTTTTAACTGTAT[C/T]TTATATGTAGATCTA | 6045 |
rs577207783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185049753 | TCTATGGACCCGGTG[C/T]TGGACTTTTGAGTAG | 6045 |
rs577263733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185052658 | GAATGCGCTAAATGC[C/T]ACTAAATGTTCAATT | 6045 |
rs577310225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185098522 | TGTGCTTTCCACCCA[A/G]AATTGCACATCTGAA | 6045 |
rs577312074 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185055087 | GGAACAAAACTATCA[C/T]TTTGCAGATTGTTTA | 6045 |
rs577325671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF2 | GRCh38.p7 | 1:185071710 | AGGTAATGCATCTCA[A/G]TGAAGTCACACAGTG | 6045 |
rs577331240 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061710 | AGATTAGAGGAAACA[A/G]CTGGTTGCTGGCTGA | 6045 |
rs577350915 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF2 | GRCh38.p7 | 1:185054743 | GTCTCTTTCGCCGGG[A/G]TTGGAGTGCAGTGGC | 6045 |
rs577597407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075246 | TGATCCCCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 6045 |
rs577605150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185064873 | AATTTCCTTTTCAGG[G/T]TGTTCATTGTTAGTG | 6045 |
rs577642145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071585 | TGTCTTCCAGGATGT[A/G]CTTGTTAAAGAGTTA | 6045 |
rs577694663 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068753 | AGTAGCCATAGAAAA[C/G]TAATATAGCAATCAT | 6045 |
rs577760199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185075971 | AGTTTAGCACAGTTT[A/G]ATTTTATTGGTTATG | 6045 |
rs577783929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185095483 | CCATTCTAGGACTCT[C/G]TAATTCCTTACCCTC | 6045 |
rs577784631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185048641 | TTGGTCATTTGTTTT[C/G]AAAAGATATGTTACT | 6045 |
rs577819339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185068048 | TTGCACTGTTGCCCA[C/T]GCTGGAGTGCAATGG | 6045 |
rs577922188 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094449 | CCTGGCCTTGGAGTC[A/G]CTTTTAAATCTCTTT | 6045 |
rs578097549 | snp | C/G | 4.97863e-05 | 0.00498906 | intron-variant | RNF2 | GRCh38.p7 | 1:185087507 | CAGACCATAGCACTT[C/G]CCTTCCAAATACTAA | 6045 |
rs578173538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081514 | TTATCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 6045 |
rs578200007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185088310 | AACATCCAGAGAAAA[A/G]GAAGGAAAAACAGGA | 6045 |
rs578218926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF2 | GRCh38.p7 | 1:185081041 | AAAGATCTATCTAGG[A/G]TATATGTTAGAAATA | 6045 |
rs745342055 | snp | C/T | 1.65501e-05 | 0.00287659 | missense | RNF2 | GRCh38.p7 | 1:185099961 | CCAGTGGCCAGTTCA[C/T]TGTGAGTATTTAAAA | 6045 |
rs745343578 | in-del | -/CAC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084000 | GGCTGGAGTGCAGTG[-/CAC]GCACAGTCGTACCTC | 6045 |
rs745376415 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097536 | AGTCTTTTGTTTAAT[A/C]AAGAAAATTATTTTT | 6045 |
rs745392792 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083389 | AGTCCCGTATTTTGT[G/T]TTAGCCTATGAACAA | 6045 |
rs745466413 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084730 | GTGCCATCTAGCCTA[A/C]TAAGCGCAATAATTT | 6045 |
rs745481831 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070215 | ATGAATATCTCATTC[A/G]GTTTTGCTAGTGAAC | 6045 |
rs745560341 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080487 | GTGACATGTTCATAA[G/T]AATTGAGATAATGAT | 6045 |
rs745607733 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095815 | TTTACAAATATTTTT[-/A]ATGTAGGTATATGTT | 6045 |
rs745666459 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090974 | AGCTCCTGGGTTAGC[A/G]TGAGAAGCTGACTAC | 6045 |
rs745726539 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057144 | GAAACCCTGTCTCTA[C/T]AAAAAAGAAAAATAA | 6045 |
rs745748083 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092567 | CTTTGTATTGAAATC[A/G]CTGATTTTTAGACAC | 6045 |
rs745792118 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063984 | CCCATCTTAAGAGCT[A/G]TAATTTAATTGTATT | 6045 |
rs745868573 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065676 | AGAAACTCCTAGACA[C/G]CTCTGAAGGAACAAA | 6045 |
rs745893862 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097938 | CATGTGGGAAACAAT[A/G]TCATCCAACTCAGAG | 6045 |
rs745909572 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078415 | TATTTACTAGCCACA[A/C]TGACCTGCTTTCTTT | 6045 |
rs745991830 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066030 | CCTTCCTTTGTCATT[G/T]CCTATATCCCATGTA | 6045 |
rs746021884 | snp | A/T | 1.7479e-05 | 0.00295621 | intron-variant | RNF2 | GRCh38.p7 | 1:185098389 | TAAATTCAGAATGTT[A/T]AATTTGGAGGTAAAA | 6045 |
rs746038931 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050656 | ATTTCTTCCTTCCAA[C/G]GTCATTAGAAAATAG | 6045 |
rs746144820 | snp | G/T | 1.64768e-05 | 0.00287021 | missense | RNF2 | GRCh38.p7 | 1:185098225 | TGATTCTGGGCTAGA[G/T]CTTGATAATAACAAT | 6045 |
rs746227716 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056495 | TCCTGAGTAGGTGGA[A/C]CTATAGGTGTCTACC | 6045 |
rs746229174 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087876 | AAACAGATGTAGCAC[C/T]AACCATGGACTTTAC | 6045 |
rs746246232 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072850 | AGTCTGAGGCAGGAG[-/A]AATCGCTTGAACCCA | 6045 |
rs746280644 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054810 | TCAAGCGATCTTGCC[A/C]CCTCAGTTTCCTGAG | 6045 |
rs746319007 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074048 | GTTTGATAATTTGCT[A/G]GAATGGCTCACAGAA | 6045 |
rs746471425 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080979 | AATTCTTAGAAATCC[A/C]TCCAATGGATTTTTA | 6045 |
rs746558631 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044027 | CAGTTTCACCATATT[A/G]GCCAGGCTGATCTCG | 6045 |
rs746583085 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062141 | TGCTTTTGAGGAAGA[A/G]AGAGGCAGGTAGCTT | 6045 |
rs746600470 | snp | C/G | 1.67181e-05 | 0.00289115 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091568 | TTAATTTTAAAGTGA[C/G]TCTTTTACAGGAGGC | 6045 |
rs746637825 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084073 | TAGCCTCCCAAGTAC[C/G]TAAAACTACAGGCAC | 6045 |
rs746662965 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054939 | TCCTGAGCACAAGCA[C/G]TCCGCCTGCCTCGGC | 6045 |
rs746752271 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068993 | AAGTTCCTTTTTTGA[C/G]TAAAATGTTTCATCC | 6045 |
rs746779534 | snp | G/T | 4.95987e-05 | 0.00497965 | intron-variant | RNF2 | GRCh38.p7 | 1:185100161 | TTATTATTGTGGTTT[G/T]TGCAGTTTTCATAAT | 6045 |
rs746882006 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069978 | CACATTAACCAAAGA[C/T]TTTAGTACTTTCAGT | 6045 |
rs746885128 | snp | C/G | 1.65072e-05 | 0.00287286 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185099947 | TTATATAGCAACAGC[C/G]AGTGGCCAGTTCACT | 6045 |
rs746898476 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055328 | TGAGCATCATGTCCA[C/T]GTCCAAAAAGTTTTA | 6045 |
rs746918217 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055910 | TTAGTGCAAAAGTGC[-/T]TTTTTTTAATGTAGA | 6045 |
rs747017565 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089685 | GGGAGCAGAGAAATG[A/G]AGCAAAAACTGGAGA | 6045 |
rs747038803 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | RNF2 | GRCh38.p7 | 1:185098202 | AACAAACGGACCAAA[A/G]CATCTGATGATTCTG | 6045 |
rs747043892 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073304 | TATTTTTAATTTTTT[A/T]AAATTTTTTTGCTGG | 6045 |
rs747106046 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047150 | CCTCACTTTTTGTAA[G/T]GATTGTAGTTATTTT | 6045 |
rs747215704 | snp | C/T | 1.70015e-05 | 0.00291555 | intron-variant | RNF2 | GRCh38.p7 | 1:185098029 | TTGTTGCTTTAAAGG[C/T]CTAAAAGTAAATTTT | 6045 |
rs747289506 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086970 | TTGATATGCTAAGTA[C/T]TTCCTGTATGCCAGC | 6045 |
rs747352439 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065815 | ACAATGTCATCTACA[A/G]AGATACTGTTTTACT | 6045 |
rs747382705 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085055 | TGTAGCAACTGTACT[A/G]CTCTTCCAACGCATA | 6045 |
rs747413664 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050400 | TCTATCCTGATTAAA[C/T]CCAATTTCATTCTTT | 6045 |
rs747470470 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086165 | TCCTCAAATTCCCCA[A/G]TCCACCTCTATAATT | 6045 |
rs747608975 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059802 | ATATTTTTATCTCTA[C/G]AAATGAATTCCTTAG | 6045 |
rs747677121 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087588 | CAAACGGAACTCAAC[C/T]ATTAAGCAAAACATG | 6045 |
rs747690275 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059741 | AAGCACGTTAATAGC[A/G]TTATTTTCCACAACT | 6045 |
rs747719294 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073914 | GAGTGCCAGACCCCA[C/T]ACATTAAGGGATCAG | 6045 |
rs747744295 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057633 | GGAATGAAAGAAGAT[A/G]GCCTGTTTCCCCATT | 6045 |
rs747754333 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058354 | CCCCATGGATACTCA[A/G]GGAGGACTGTACTCT | 6045 |
rs747767816 | snp | A/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043808 | CCTGATTATTTTGAT[A/T]TTGTTGTTGTTGTTG | 6045 |
rs747853191 | snp | A/T | 1.72291e-05 | 0.002935 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100336 | GAGACTGAACTTTTT[A/T]ATAGCCTATTTCTTT | 6045 |
rs747992559 | in-del | -/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043825 | GTTGTTGTTGTTGTT[-/G]TTGTTTTGTTTTGAG | 6045 |
rs748056780 | in-del | -/C | 1.67186e-05 | 0.0028912 | intron-variant | RNF2 | GRCh38.p7 | 1:185099787 | TAATGATTTATTCTT[-/C]TAGATACATAAAGAC | 6045 |
rs748082234 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068738 | TTGTGATAATGTTAC[A/G]GTAGCCATAGAAAAC | 6045 |
rs748099631 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096835 | ATTTTATAAGCAGGA[-/T]TTTTTTTTTTTTTTT | 6045 |
rs748154792 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069812 | CTTCTTTTTCCCTTA[A/G]GCTTCCAGGAACCAA | 6045 |
rs748212169 | snp | C/G | 1.68903e-05 | 0.00290601 | intron-variant | RNF2 | GRCh38.p7 | 1:185093024 | AGCCCAAAGATACTA[C/G]CATTGTTTACATTTG | 6045 |
rs748218652 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053817 | GTAGTATTAGGTCTT[G/T]TGTGCCTGTGTTTTA | 6045 |
rs748323619 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075274 | GCTGGGATTACAGAC[A/G]TGAGCTACTGTATTG | 6045 |
rs748355743 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090592 | TTTGTGGAGTAATCC[A/G]TCTTTGACCATATAA | 6045 |
rs748367762 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089517 | GAGTAGATTGTACAA[C/G]TTTGAGGGTTGATTG | 6045 |
rs748422837 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091524 | TTTTATATGTTTGAG[C/T]TTGTCCATAATAAAA | 6045 |
rs748485073 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076582 | TGAGCCACTGCGCCC[A/G]GCCTTATTTTATGGT | 6045 |
rs748574979 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064203 | AGCTTCTATATAGTA[A/G]GTTATGATTAATGTT | 6045 |
rs748605758 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050305 | AATAGCAAATGAGTG[C/T]TATGTTTTGGGAGCC | 6045 |
rs748615671 | in-del | -/TA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050306 | ATAGCAAATGAGTGC[-/TA]TGTTTTGGGAGCCCA | 6045 |
rs748683116 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073530 | CATCTATTTTTCAGA[C/T]ACTGTCTTTTGATCT | 6045 |
rs748699527 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050313 | ATGAGTGCTATGTTT[C/T]GGGAGCCCAAAAGAC | 6045 |
rs748725375 | snp | C/T | 2.23321e-05 | 0.00334149 | intron-variant | RNF2 | GRCh38.p7 | 1:185093325 | TTTTTCTGAATACTT[C/T]ATTAACAATTAAATT | 6045 |
rs748752790 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063642 | AAACTTACTATTTTA[C/T]AGTTCTGGCAGTAAG | 6045 |
rs748805591 | snp | A/C | 1.68587e-05 | 0.00290329 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100319 | CTTTAAAAACCAATT[A/C]TGAGACTGAACTTTT | 6045 |
rs748851809 | snp | C/T | 1.79842e-05 | 0.00299863 | intron-variant | RNF2 | GRCh38.p7 | 1:185100181 | GTTTTCATAATTTTT[C/T]CTTTCTTTTTTGTTT | 6045 |
rs748855501 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072305 | GGTTGCCTAATTTGA[A/G]CTCCTCTTTTTATTT | 6045 |
rs748883460 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071358 | CTGAAAGATTAAGAC[A/G]AGGGAAGCCATCTTG | 6045 |
rs749017382 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058324 | GTGTCTGTGGTGTGC[A/G]GGGTATCTTCAGAAC | 6045 |
rs749031386 | snp | A/G | | | missense | RNF2 | GRCh38.p7 | 1:185093119 | AGATCACTAAGGCCA[A/G]ACCCAAACTTTGATG | 6045 |
rs749041715 | in-del | -/CTTG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094103 | AATTCCATCATTCTA[-/CTTG]CTTAAGCCAAAAACT | 6045 |
rs749099110 | in-del | -/TG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090768 | TAGAGCTGAGTAATC[-/TG]TGTTCTCACTGCCAG | 6045 |
rs749108671 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078586 | GTACTTAGTGATCTT[G/T]CATATGAATATGAAG | 6045 |
rs749171239 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043699 | CTTTAATTGAACTAC[A/G]CATGCACTCGTCATG | 6045 |
rs749196176 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079777 | CTACTAAAAGTACAA[A/G]AATTAGCCAGGTGTG | 6045 |
rs749354075 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067358 | GTTGGATTGCTTACT[C/G]ACAATTTATTATTTG | 6045 |
rs749392060 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052627 | GGAACTAGGGTTAGT[A/G]GCTGCACAAGACTGT | 6045 |
rs749442093 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068449 | TGTTACCACATGTAA[C/T]TTTATAAGAGAAGGG | 6045 |
rs749465137 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053749 | CAAAACAATGTGTGG[G/T]ACGTAATAGGCTCTC | 6045 |
rs749515485 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066308 | CTGTACTCCCCACCT[C/T]CTTTTCCACTCATTT | 6045 |
rs749520623 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094834 | TTTATTCAGGCCTCA[A/G]GGAGAATCATTATTT | 6045 |
rs749568471 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067783 | TGATGCAATCTCGGC[C/T]CTCGGCAACCTCTGC | 6045 |
rs749584147 | in-del | -/TTTC | 5.44667e-05 | 0.00521828 | intron-variant | RNF2 | GRCh38.p7 | 1:185100179 | CAGTTTTCATAATTT[-/TTTC]TTTCTTTTTTGTTTT | 6045 |
rs749585829 | snp | C/G | 0.000197772 | 0.00994217 | missense | RNF2 | GRCh38.p7 | 1:185099907 | AGATGAACCTTGATA[C/G]AGCCAGTGAGAAGCA | 6045 |
rs749620307 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089502 | AGAGCACGTTCACCT[G/T]AGTAGATTGTACAAG | 6045 |
rs749622318 | in-del | -/TGAA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052749 | GTGAGCTGAAAAGTT[-/TGAA]TGAGGCATAGGCTCC | 6045 |
rs749633339 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074286 | TGGACATGACTGGTT[A/G]AATCATTGGCCATTG | 6045 |
rs749662672 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053266 | TAGTTTTCCCCCTAC[A/G]TTTATTTTTATGTTG | 6045 |
rs749684083 | in-del | -/TTTAATA | 3.56322e-05 | 0.00422076 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100349 | TTTATAGCCTATTTC[-/TTTAATA]TTAAAGATGTACTGG | 6045 |
rs749688373 | snp | G/T | 1.79593e-05 | 0.00299655 | intron-variant | RNF2 | GRCh38.p7 | 1:185093294 | ATATGGGAAAGAGGG[G/T]CAGAGAGGGTAGCTG | 6045 |
rs749688644 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062542 | ATCCTCTTTACATGT[A/C]AAAAAAAATTGCAAG | 6045 |
rs749703176 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054645 | ATTGTCTTTCAAGAT[A/T]GACATGTCGCCTCAG | 6045 |
rs749777852 | in-del | -/A | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101770 | CCGGTATGAAAACTT[-/A]AAAGGTATATATTCA | 6045 |
rs749820028 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063926 | CCTCTTAAGGACCTT[G/T]GCAGTTACATTGTGC | 6045 |
rs749928738 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | RNF2 | GRCh38.p7 | 1:185098096 | AGGCAAGAAACAACA[C/G]ATTGAAAATGGTAGT | 6045 |
rs750031835 | snp | C/G | 1.65789e-05 | 0.0028791 | missense | RNF2 | GRCh38.p7 | 1:185093182 | GAGTATGAAGCTCAT[C/G]AAGAGAGAGTATTAG | 6045 |
rs750050569 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101118 | TTTCCTGTATTATAT[G/T]TGATGTTTTTCCCCA | 6045 |
rs750088173 | in-del | -/CAGACAAACGGAAC | 1.64754e-05 | 0.00287009 | frameshift-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087569 | ATGTCTCAGGCTGTG[-/CAGACAAACGGAAC]TCAACCATTAAGCAA | 6045 |
rs750124241 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051319 | GTGTATAGTAGGAGT[A/T]GCAGAATTGAATGCA | 6045 |
rs750161503 | snp | A/G | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102781 | TTTGTTTATCCATTC[A/G]TCTGTTGATGGAGAC | 6045 |
rs750282271 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072180 | CTGGCTAGGGTGGGG[G/T]TTCCAAGCACAGTTG | 6045 |
rs750300701 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073688 | TTACAAGGAATGCAG[A/G]TAAGACAATTACATC | 6045 |
rs750307173 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101346 | ATTTGGCGCTCTTTT[-/A]ATTACACTCTGTAGA | 6045 |
rs750371339 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090868 | AATTTTACATTGGAA[A/C]TCCAGATGCATTTTG | 6045 |
rs750388602 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059465 | GAACATAACTTTTAC[A/G]TAGCTGTCCTTGTAG | 6045 |
rs750456952 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101160 | GAGATAATGGAGATA[-/T]TTTGCACTTTAGCCT | 6045 |
rs750497470 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094028 | CATCTCAAACTTAAC[A/G]TGATGAATACTGAAC | 6045 |
rs750499856 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062012 | AAAATTTGTGCTTAC[C/T]CCTGTTTCAGTAACC | 6045 |
rs750578712 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043444 | TAAGGATGTTAGCCT[C/G]AGGTCTAGCTTTTTA | 6045 |
rs750587509 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095416 | CTTCCAAATAATCCA[A/C]ATGGCACACTACCTC | 6045 |
rs750628912 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068295 | GTGGTAGGCTGAAAA[A/G]TGTCCCCCAAAAGAT | 6045 |
rs750656273 | snp | A/T | 1.6537e-05 | 0.00287545 | intron-variant | RNF2 | GRCh38.p7 | 1:185091745 | TTAGAAGTGGGTATG[A/T]TGAAAAGAGTTGTTA | 6045 |
rs750661158 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083940 | TTAAGTCTTTTCCTT[-/A]AAAAAAAAAAAAAAA | 6045 |
rs750662749 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073129 | CAGTGTTTATAGCTA[C/T]GTAGTATTCTATACT | 6045 |
rs750771376 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083859 | TGATCTACCTGTCTC[A/G]GCCTCCCAAAGGGCT | 6045 |
rs750837727 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069602 | ACCAAAGAGTAAAGG[C/T]CATGTAGATTCTGTA | 6045 |
rs750966216 | snp | A/G | 1.6691e-05 | 0.00288881 | intron-variant | RNF2 | GRCh38.p7 | 1:185099996 | AGACTGTTGAAACTG[A/G]GAGCACACTGACCAA | 6045 |
rs751001811 | in-del | -/T | 0.000184108 | 0.00959271 | intron-variant | RNF2 | GRCh38.p7 | 1:185098052 | AAATTTTATGCATCC[-/T]TTTTTTCCCCCTTGA | 6045 |
rs751061208 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048480 | AATTAACATGTTTGC[A/C]ATTTATCATAATTTT | 6045 |
rs751063882 | in-del | -/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045207 | GGTGGGCCGAAGCCA[-/G]GGCAGAAGAACCCAA | 6045 |
rs751093217 | snp | C/T | 8.28837e-05 | 0.006437 | intron-variant | RNF2 | GRCh38.p7 | 1:185091775 | ATACTAGGTACTTAA[C/T]TGTACCACGAAAGTG | 6045 |
rs751096621 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075828 | CACATGAGATTTGGG[C/T]GAAGCCACAAATCTT | 6045 |
rs751197296 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063712 | TGGAAGGTCTGTGAC[G/T]TTTCTGGAGTCTCTA | 6045 |
rs751334934 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098446 | AATATTTGTCATCCC[A/G]TTGATTGCAGGGGTT | 6045 |
rs751412116 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084557 | GTTTTCAAGTCAGTT[C/T]TATTTTGAGACCTTG | 6045 |
rs751428857 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071204 | GTCAGTTACGCATTC[A/G]TCTCAGGGTAGGCCA | 6045 |
rs751518734 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185071990 | AGTAGTAAGACATGA[A/G]TAGGTAGATGTGGAG | 6045 |
rs751537098 | snp | A/G | 1.65416e-05 | 0.00287586 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093148 | TGCACTCATCAGCAA[A/G]ATTTATCCAAGTCGT | 6045 |
rs751643641 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076581 | GTGAGCCACTGCGCC[C/T]GGCCTTATTTTATGG | 6045 |
rs751699242 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058039 | TTGAGGTGGGAACAT[C/T]ACCGGAGCCTGGGAG | 6045 |
rs751714391 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059297 | ATCTACCTATGTGAC[A/G]GGGGACACAGGAAAC | 6045 |
rs751794692 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093836 | CCCAACTGTGAAATA[C/T]GGCGTGTCCCAGAGA | 6045 |
rs751849393 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079480 | TGTTTTAACCTTTTA[A/G]AGGAAAGCATCTTTG | 6045 |
rs751869611 | snp | C/T | 3.29815e-05 | 0.00406075 | intron-variant | RNF2 | GRCh38.p7 | 1:185087543 | TTTTTCTCTCTTCTT[C/T]ATTTCCAGCAATGTC | 6045 |
rs751947086 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095208 | TTCAGTTTAGCCTTT[G/T]ACTAAAAGCAAGACT | 6045 |
rs751951730 | snp | C/T | 1.65269e-05 | 0.00287457 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185099821 | TGGTAACGCCACTGT[C/T]GATCACTTATCCAAG | 6045 |
rs751988846 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065333 | CAGTAGGATGTGGGC[-/A]AGGGCCAAATAAGGG | 6045 |
rs752025989 | in-del | -/TC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049391 | AATTATTTCTCATTT[-/TC]TCTCATTTAAACAGT | 6045 |
rs752058895 | snp | C/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103074 | TATATTAATGGGTAT[C/T]CTTATGATAGCTGTC | 6045 |
rs752175054 | snp | C/G | 1.6817e-05 | 0.0028997 | intron-variant | RNF2 | GRCh38.p7 | 1:185098351 | ACAGACGAGGTAAGT[C/G]TGTGGATTAGTTTCA | 6045 |
rs752227521 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087779 | CTGTATGTTGGCTAA[C/T]ACTTTATTCATTGAT | 6045 |
rs752282447 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051645 | GTGTTTAGGGTGGTA[A/T]TGGGGTGTGGGAGGA | 6045 |
rs752325303 | in-del | -/CTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056620 | AAGTGATCCTCCCTC[-/CTT]GGCCTCCCAAAGTGC | 6045 |
rs752331698 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074842 | ACAGGAGGAGGGTAT[A/G]TGTAAGTTATATGCA | 6045 |
rs752402538 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090197 | AGTGCTGGAATTACA[A/G]GTGTGAGCCATCGTG | 6045 |
rs752504954 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097134 | TCTTTGCTTTTCTCA[A/G]CTAGAAAATGACATT | 6045 |
rs752554954 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047411 | CCCAGGTTTGAATGG[A/G]TAGAAATATAGACCA | 6045 |
rs752592915 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097861 | TAAGTGAATAGAAAC[A/G]TTCGTTAAATTATTT | 6045 |
rs752806343 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185071905 | CAGCTCTGTCACTTT[C/G]TCATTATATTTTCTC | 6045 |
rs752851997 | snp | A/G | 1.65748e-05 | 0.00287874 | intron-variant | RNF2 | GRCh38.p7 | 1:185087514 | TAGCACTTCCCTTCC[A/G]AATACTAAAATTGTT | 6045 |
rs752910072 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056224 | AGTGTAGATAACATT[A/G]TTAATGTCAGTTTAA | 6045 |
rs752999829 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057769 | TTTCGTATCCTTGGA[G/T]TCAACAGACTGCAGG | 6045 |
rs753036759 | snp | A/G | 1.65693e-05 | 0.00287826 | missense | RNF2 | GRCh38.p7 | 1:185100290 | TACGCACCTACAAAG[A/G]AGCACAAATGAGCCT | 6045 |
rs753063280 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067708 | AATTTAAAAGTATCC[-/T]TTTTTTTTTTTTTTT | 6045 |
rs753122163 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078074 | AACATGGGTGAAACC[C/G]TGTTTCTACTAAAAA | 6045 |
rs753138560 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065576 | AACAACTCCAGACGC[G/T]CCACCTTTAAGAGCT | 6045 |
rs753166572 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093731 | TAATTTTCTTCACCT[G/T]GCTTTCAGGAGGCCA | 6045 |
rs753192062 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | RNF2 | GRCh38.p7 | 1:185098140 | ATGGTGACAGTTCAC[A/G]CTGCAGTAATGCATC | 6045 |
rs753241461 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090602 | AATCCATCTTTGACC[A/G]TATAAAGAAAGCACA | 6045 |
rs753259892 | in-del | -/GGTTA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099365 | AATGAACATTTCTAT[-/GGTTA]GTCTTAAAAGACATT | 6045 |
rs753331349 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051883 | ATATATGTAAAAATG[C/T]GTGTATGTAAAAAGT | 6045 |
rs753355359 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065540 | GAAGTCAGCCAGACC[A/G]TGAACCCACCAGGAG | 6045 |
rs753394109 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101777 | TGAAAACTTAAAGGT[A/G]TATATTCAATTTTTT | 6045 |
rs753397517 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093683 | CGTTACTTAGCAGCA[C/T]TTGACACAATTAATT | 6045 |
rs753412436 | snp | A/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102875 | TTCTGTTATTTTGGG[A/T]ATATATGAAGGAATA | 6045 |
rs753487875 | snp | A/T | 1.64808e-05 | 0.00287057 | missense | RNF2 | GRCh38.p7 | 1:185098277 | GTAATGGATGGTGCT[A/T]GTGAAATTGAATTAG | 6045 |
rs753516093 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052882 | TCAAGTAATGACGGT[G/T]ATAATAAGAGATGGC | 6045 |
rs753549854 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067125 | CAATCAAATTAGGAA[A/T]TGATATTGCTTCTTT | 6045 |
rs753614025 | in-del | -/ATT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049377 | ACTTGCACTTTTAAA[-/ATT]ATTTCTCATTTTCTC | 6045 |
rs753614736 | snp | A/C | 1.64773e-05 | 0.00287026 | missense | RNF2 | GRCh38.p7 | 1:185098116 | AAAATGGTAGTGGAG[A/C]AGAAGATAATGGTGA | 6045 |
rs753646024 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074777 | AATTATTTACATAGC[A/G]TTTACATTGTATTGA | 6045 |
rs753648935 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073802 | ATTTCTGACACTAAA[G/T]ATGTGGTTTTTTGCT | 6045 |
rs753652851 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052275 | TGTAACACACAGGTT[A/C]CTGGCACCGCTATTC | 6045 |
rs753656123 | snp | C/T | 1.64746e-05 | 0.00287002 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087573 | CTCAGGCTGTGCAGA[C/T]AAACGGAACTCAACC | 6045 |
rs753664788 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088769 | CACAAAGTTCCAAAA[A/G]CCAAAATTTGAATTT | 6045 |
rs753678396 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095569 | ACTAGAATTATGACC[C/T]CTAAGAGGGAAGAGA | 6045 |
rs753694062 | snp | C/G | 1.65023e-05 | 0.00287244 | intron-variant | RNF2 | GRCh38.p7 | 1:185087680 | GGGCATATGAGACGT[C/G]TAAACTGGGATACAT | 6045 |
rs753724516 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049759 | GACCCGGTGCTGGAC[-/T]TTTGAGTAGGTCAGC | 6045 |
rs753736561 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059621 | TGGCATTATTGTTGT[A/G]GTAGCAGTAGTAATA | 6045 |
rs753763573 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095607 | GTATCATTGATTCTT[-/A]ATTAACACCATTATT | 6045 |
rs753778111 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045247 | TGAGCACGAGGTGGC[C/T]GCGCCGTCATCCGGG | 6045 |
rs753943567 | snp | A/G | 6.7113e-05 | 0.00579241 | intron-variant | RNF2 | GRCh38.p7 | 1:185100014 | GCACACTGACCAACT[A/G]ACTGAGTGGCAAGTG | 6045 |
rs753944142 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081513 | ATTATCCTGCCTCAG[C/T]CTCCTGAGTAGCTGG | 6045 |
rs753977672 | snp | C/T | 1.65397e-05 | 0.00287569 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100244 | GGTCAGTGAGAAATA[C/T]TGGAAAGTGAACAAA | 6045 |
rs754219495 | in-del | -/CTTTCCC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092164 | TTTCTCCTTTTTCTT[-/CTTTCCC]CTTTCCCCTTTCCTT | 6045 |
rs754297690 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056138 | TAGTCTTCTGAAATA[C/T]TTTTTTCAGGAGTTC | 6045 |
rs754301157 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076094 | AATTTACATATGTTG[C/G]ACATATTTTTTTCCT | 6045 |
rs754507437 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051985 | GCATGCACCCATGTA[A/G]CACTTCTCAAATTAA | 6045 |
rs754554977 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085714 | GCTGGAGTGCAATGG[C/G]GCGATCTCAGCTCAC | 6045 |
rs754565170 | in-del | -/ATT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059610 | CTTCATGTTAATGGC[-/ATT]ATTGTTGTAGTAGCA | 6045 |
rs754565449 | in-del | -/CC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092175 | TCTTCTTTCCCCTTT[-/CC]CCTTTCCTTTCCTTT | 6045 |
rs754699271 | in-del | -/TG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072216 | ATAAACCAAGGTGAC[-/TG]TGAAGAATATCTGGA | 6045 |
rs754718586 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059650 | TAATCATATGTTTGG[G/T]TGGGGGCTAAGAGCA | 6045 |
rs754781881 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | RNF2 | GRCh38.p7 | 1:185087682 | GCATATGAGACGTGT[A/G]AACTGGGATACATTT | 6045 |
rs754789001 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074804 | TTGAGTATTGTAAGT[A/G]ATCTAGAGATGATTT | 6045 |
rs754795939 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097395 | CCTTAAGAATTTCTT[C/T]AAAGAGGCATAAATA | 6045 |
rs754850797 | snp | A/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045251 | CACGAGGTGGCTGCG[A/C]CGTCATCCGGGCGTT | 6045 |
rs754939999 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097089 | AGCTGTATAACTGGA[A/G]GCAAATTATTTAATC | 6045 |
rs754943521 | snp | A/T | 4.9423e-05 | 0.00497082 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087575 | CAGGCTGTGCAGACA[A/T]ACGGAACTCAACCAT | 6045 |
rs754956367 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082853 | ATGAACAGCAAGTAA[C/T]AAGTCGTTAGCAAAA | 6045 |
rs754988267 | in-del | -/T | 1.68815e-05 | 0.00290525 | intron-variant | RNF2 | GRCh38.p7 | 1:185098358 | AGGTAAGTGTGTGGA[-/T]TAGTTTCAGATTATC | 6045 |
rs755010960 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081782 | AGAATTGGGCCCTTT[C/T]TGTTGATCAGTGCCA | 6045 |
rs755011627 | in-del | -/AT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051954 | TATATACATTTTTAC[-/AT]ATATATATATATATG | 6045 |
rs755143306 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069765 | GCTAATTTCTAATGA[A/C]ATTTAAGCCCGAAAT | 6045 |
rs755215668 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052644 | CTGCACAAGACTGTG[A/C]ATGCGCTAAATGCCA | 6045 |
rs755284460 | in-del | -/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101537 | TAAGATTGACTTGGG[-/T]TGTTATATTTCATCT | 6045 |
rs755360567 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092126 | GAGTCACTGCACCTG[A/G]CCGAGAAATACATTT | 6045 |
rs755364780 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076436 | GCTGGGACTACAGGC[A/G]CGTGCCTCCATGCCT | 6045 |
rs755384125 | snp | A/C | 1.64776e-05 | 0.00287028 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098117 | AAATGGTAGTGGAGC[A/C]GAAGATAATGGTGAC | 6045 |
rs755473078 | snp | C/G | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185103003 | TGAACAAGCGTTCTG[C/G]CTTTTCCGTATCCTC | 6045 |
rs755483813 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064074 | GACACCTTTGGGGAC[C/G]TATTATTCACACTGC | 6045 |
rs755616880 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098883 | CAGCCTCCCGAGTAG[C/T]TGGGACTACAGGCTC | 6045 |
rs755640832 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065471 | CTCTTTGGGTCGGCA[C/G]TACTACCTTTATGAG | 6045 |
rs755676091 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051348 | CAGGAGACTTGGTTT[C/T]TAGGTCTGGTTCCAC | 6045 |
rs755677621 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050096 | ATGATCTGGACGAAT[A/G]GTGTAGGTTAAGATG | 6045 |
rs755683318 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088603 | AGGAGGATGTAGTTA[A/C]AGTGTTTAACACTAG | 6045 |
rs755707192 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101570 | CTCCAGACTCTAGGT[A/G]TATTTCCAACTTTAT | 6045 |
rs755723238 | snp | A/G | 1.66621e-05 | 0.00288631 | missense | RNF2 | GRCh38.p7 | 1:185093216 | GGATCAACAAGCACA[A/G]TAATCAGCAAGCACT | 6045 |
rs755760055 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085814 | GCGCACCACCACACC[C/T]GGCTAATTTTTGTAT | 6045 |
rs755902637 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058177 | CTAGCAACTAGTTAC[A/G]TAGCATTTATATTGT | 6045 |
rs755914903 | in-del | -/TGTCACGTC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047474 | ACCTACAGTTTGTGG[-/TGTCACGTC]TGTGTCTCTAATCTG | 6045 |
rs755965502 | snp | A/T | 8.24599e-05 | 0.00642053 | intron-variant | RNF2 | GRCh38.p7 | 1:185087544 | TTTTCTCTCTTCTTT[A/T]TTTCCAGCAATGTCT | 6045 |
rs755975267 | in-del | -/A | 3.324e-05 | 0.00407663 | intron-variant | RNF2 | GRCh38.p7 | 1:185099980 | AGTATTTAAAATAAT[-/A]AGACTGTTGAAACTG | 6045 |
rs756044862 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046190 | CGGGGTTCCAGTGTA[A/G]AGGAGCTCCTCGACC | 6045 |
rs756096696 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059482 | AGCTGTCCTTGTAGC[A/G]CAGATGCAAATTAGT | 6045 |
rs756107760 | snp | A/G | 1.66771e-05 | 0.00288761 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100309 | ACAAATGAGCCTTTA[A/G]AAACCAATTCTGAGA | 6045 |
rs756151665 | snp | A/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043479 | CATTTAATCCAGATA[A/T]CCCATAAGTTTTCCG | 6045 |
rs756216909 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054432 | GTCCTGGGGCACGTC[C/T]GGTGATAGCTGGGCC | 6045 |
rs756233391 | snp | C/T | 1.64827e-05 | 0.00287073 | missense | RNF2 | GRCh38.p7 | 1:185099900 | TCAAACCAGATGAAC[C/T]TTGATACAGCCAGTG | 6045 |
rs756448917 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068328 | CTACATTCTGGTCTC[C/T]GGAACCTGTAAATGT | 6045 |
rs756486168 | snp | A/G | 4.98451e-05 | 0.004992 | intron-variant | RNF2 | GRCh38.p7 | 1:185091784 | ACTTAATTGTACCAC[A/G]AAAGTGCTTTCCAGG | 6045 |
rs756494040 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053459 | CCCGCCTCAGCCGCC[G/T]TTGTAGCTGAGATTA | 6045 |
rs756538828 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069615 | GGCCATGTAGATTCT[A/G]TATACTTTAGCCCTA | 6045 |
rs756619310 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075029 | GAGATGGAGCCTTGC[C/T]CTGTCGCCCAGGCTG | 6045 |
rs756654631 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054494 | CATCTGGGTCTCTGG[-/C]CCCTCCGGGCCGGCC | 6045 |
rs756785364 | snp | C/G | 1.65466e-05 | 0.00287628 | missense | RNF2 | GRCh38.p7 | 1:185093155 | ATCAGCAAAATTTAT[C/G]CAAGTCGTGATGAGT | 6045 |
rs756828924 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063744 | GGGAGAATTCATTTT[C/T]TTTCATTTTCTAACT | 6045 |
rs756883144 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067239 | AACACTTTGTGTCTT[C/T]AGAAGCTTACAGAAA | 6045 |
rs756914724 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047738 | ATGACTCATTAAATT[C/G]TGGATAAACTAAAAA | 6045 |
rs756923280 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098473 | GGTTCAGTTACTAGC[G/T]GCCTAGATTGTTGTT | 6045 |
rs756985306 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084591 | TGCTGGTCACAAAAG[A/G]CCATTGCATATTTGG | 6045 |
rs757071210 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085660 | TCTCCTGTTTAAAAC[A/T]TTTTTTTTTTTGAGA | 6045 |
rs757075058 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071211 | ACGCATTCATCTCAG[G/T]GTAGGCCAAGGGATG | 6045 |
rs757105375 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089135 | ATAATAAGGAGCATG[C/T]AGTCTAGATCCGTTG | 6045 |
rs757106486 | snp | A/C | 4.99106e-05 | 0.00499528 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100304 | GGAGCACAAATGAGC[A/C]TTTAAAAACCAATTC | 6045 |
rs757118344 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049617 | AGAAAACGGAGACTT[C/T]AGTAAGAATTTCAAC | 6045 |
rs757159340 | snp | A/G | 1.84018e-05 | 0.00303324 | intron-variant | RNF2 | GRCh38.p7 | 1:185100163 | ATTATTGTGGTTTGT[A/G]CAGTTTTCATAATTT | 6045 |
rs757235813 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090633 | AGTATGATGGACTGC[C/G]AGTGGAAACAGGAAG | 6045 |
rs757309039 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078215 | TCTTGTCACTGCATT[C/G]CAGCCTGGGTGACAA | 6045 |
rs757313855 | snp | C/T | 1.7146e-05 | 0.00292792 | intron-variant | RNF2 | GRCh38.p7 | 1:185098374 | TAGTTTCAGATTATC[C/T]AAATTCAGAATGTTT | 6045 |
rs757343045 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092469 | CGTGAGCCACCGTGC[C/G]TAGCCGAGAAATACA | 6045 |
rs757430900 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093966 | TTATATATCCAGCCC[A/G]GACTTACCTGAATTT | 6045 |
rs757437238 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102160 | TATGGGAGGATATAA[A/G]CTGCATCATTAGTGA | 6045 |
rs757523071 | in-del | -/AC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051818 | TTTTTACATATATAT[-/AC]ACACATTTTATGTAT | 6045 |
rs757546179 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081034 | TTCTCTGAAAGATCT[A/G]TCTAGGATATATGTT | 6045 |
rs757626545 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067052 | GACCGGATAATGGAG[A/C]TTTGGCAAATTACCT | 6045 |
rs757679195 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056120 | TGCTCTGTGATGATT[A/T]GTTAGTCTTCTGAAA | 6045 |
rs757710931 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053296 | GATCCACATACTCCT[A/G]TCATTATTTTCTCAC | 6045 |
rs757760160 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080119 | CTCACTTCGTATCTT[C/G]TTTGCTGGCTTCCAC | 6045 |
rs757894561 | snp | A/G | 1.65277e-05 | 0.00287464 | intron-variant | RNF2 | GRCh38.p7 | 1:185087689 | AGACGTGTAAACTGG[A/G]ATACATTTTTAGAAC | 6045 |
rs757971537 | in-del | -/TC | 1.64792e-05 | 0.00287042 | intron-variant | RNF2 | GRCh38.p7 | 1:185087649 | CCTCAGGTAATGACT[-/TC]AAGATGACTGCCAAG | 6045 |
rs757997673 | in-del | -/TTTT | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043521 | ATTCTCCTGTGAGTC[-/TTTT]TTAAGCACTATATTT | 6045 |
rs758001930 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044951 | ACCACAATCAGAATG[C/T]TAAGCTAAGTTTAGA | 6045 |
rs758001949 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083961 | AAAAAAAAAAATTAG[G/T]GGTGGGATCTCACTC | 6045 |
rs758015755 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074922 | ATCGGGGAGGGGGAG[C/T]TCAGAGGGTGTCCTG | 6045 |
rs758073653 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | RNF2 | GRCh38.p7 | 1:185099922 | CAGCCAGTGAGAAGC[A/G]GTATACCATTTATAT | 6045 |
rs758098090 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045264 | CGCCGTCATCCGGGC[A/G]TTGCCCGGGGGCTAC | 6045 |
rs758105559 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095999 | CTTAATGTTCTTTAT[A/G]TGAACATATTCTTTA | 6045 |
rs758127670 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099382 | TAGTCTTAAAAGACA[-/T]TTTTAATTCTTAGAC | 6045 |
rs758173167 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061357 | TGGTCTCAAGACCCT[A/G]TCTCTTAAAAGGGGA | 6045 |
rs758235816 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047571 | CCTAATGAATAATAT[A/G]TAACCAGATGTTTCA | 6045 |
rs758239181 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065763 | GTTCTTGAAGTCAGC[A/G]AGAGCAAGAAACCAC | 6045 |
rs758265209 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065956 | TGCTATACTGTCTCA[-/T]TTTTTTTTTTTTTAG | 6045 |
rs758338389 | snp | A/C | 1.65745e-05 | 0.00287871 | intron-variant | RNF2 | GRCh38.p7 | 1:185091770 | TTGTTATACTAGGTA[A/C]TTAATTGTACCACGA | 6045 |
rs758413271 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056733 | TCAATATGTTGCTTA[A/G]TCCTTTTGGAGGTAG | 6045 |
rs758501126 | snp | G/T | 3.30715e-05 | 0.00406628 | intron-variant | RNF2 | GRCh38.p7 | 1:185087526 | TCCAAATACTAAAAT[G/T]GTTTTTCTCTCTTCT | 6045 |
rs758571203 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049954 | TCCAGTCTTCACTTA[-/C]TGCTGCTATTGGCAA | 6045 |
rs758591224 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073190 | TTGACATAGATTTTT[A/G]TGGGTTTTTTGCTAC | 6045 |
rs758703947 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078123 | GTAGTGGTGTGTGCC[C/T]GTAGTCCCAGCTGCT | 6045 |
rs758717028 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092365 | TATTTTTAGTAGAGG[A/G]GGGCTTTCACTGTGT | 6045 |
rs758767552 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056802 | ACTTAAAATGTCTTT[G/T]AATAAAATAGTATTC | 6045 |
rs758795563 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065644 | AAGTCAGCGAGACCA[C/T]TAACTCACCGGAAGG | 6045 |
rs758849616 | snp | A/G | 1.65488e-05 | 0.00287647 | missense | RNF2 | GRCh38.p7 | 1:185098329 | TTATGGAAAAAGATG[A/G]CAGTGCACAGACGAG | 6045 |
rs758860669 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | RNF2 | GRCh38.p7 | 1:185098170 | CCACACATAGCAATC[A/G]GGAAGCAGGCCCTAG | 6045 |
rs758866253 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085466 | ATACCAGTGTTTTGT[A/G]TATCATTTAGTGCTC | 6045 |
rs758912453 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097982 | CAGTATTTTTTGGAA[C/T]TCTAAAGTTCAGTAG | 6045 |
rs758962313 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082453 | CCTCCCAGGTTCAAG[C/T]GATCCTCCTGCCTCA | 6045 |
rs758970629 | in-del | -/CA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047847 | TAATTCGTGTTATTG[-/CA]CACACTGTAGAAGAC | 6045 |
rs758995490 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058797 | TTATTGTTTGGAGCT[C/G]TTTGCAATATTTCCA | 6045 |
rs759032491 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101914 | ACTTTTATATATTCA[A/G]TTCCTTTTCTGGTGT | 6045 |
rs759053147 | in-del | -/ATT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049429 | GTTTAAATCACAAAA[-/ATT]ATTTTTATGCTGCAG | 6045 |
rs759061238 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053023 | CATTATAGACAAGGA[A/G]ACTGAGGAATTAAGA | 6045 |
rs759217170 | snp | A/G | 3.61141e-05 | 0.00424921 | intron-variant | RNF2 | GRCh38.p7 | 1:185099758 | TCATTGGCATATTCT[A/G]GAAATGAAATTTTTA | 6045 |
rs759270328 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051043 | ATTGCGAAATGTGCA[A/G]ATCGACAGTACTTCA | 6045 |
rs759270448 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | RNF2 | GRCh38.p7 | 1:185098284 | ATGGTGCTAGTGAAA[C/T]TGAATTAGTATTCAG | 6045 |
rs759305422 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088914 | TTTCATCCATGTGCT[A/G]ATAAGTACTATGTTG | 6045 |
rs759343093 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063152 | ATGAGTGAATTCTGA[A/G]CAATGTCTTTATTTG | 6045 |
rs759411297 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075555 | TTTAGTTGGCTCAAG[A/G]TTCTGCAAGGCTGTA | 6045 |
rs759430204 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061150 | TTTTTTTTTTTGAGA[C/T]GGAATCTCGCTCTGA | 6045 |
rs759607178 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047183 | TCAGGTATCCTTGTG[G/T]CATCCACATTTGAGG | 6045 |
rs759710483 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049020 | ATCACGAGGTCAAGT[A/G]TTCGAGACCAGTCTG | 6045 |
rs759783174 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082676 | ACTTCTTTCTTGGAC[C/G]ACCACTGCCCTGTAC | 6045 |
rs759826031 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090142 | GGTCAGGCTGGTCTC[A/G]AACTTCTGACCTTGT | 6045 |
rs759890298 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070847 | TTCACCGTATTAGCC[A/G]GGATGGTCTCGATTT | 6045 |
rs759921518 | snp | A/T | 1.64795e-05 | 0.00287045 | intron-variant | RNF2 | GRCh38.p7 | 1:185087650 | CCTCAGGTAATGACT[A/T]AGATGACTGCCAAGG | 6045 |
rs759944117 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064796 | CAAGTCTTGTGCCTC[C/T]TTGGCTTAAGTTTAT | 6045 |
rs759968011 | in-del | -/TTA | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070161 | ATGATATCACCTAGT[-/TTA]TTATGATTGTCATGT | 6045 |
rs759975864 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185071829 | TCAACCTGCCCTCCC[A/G]TTCATTATGGTCTGG | 6045 |
rs760018174 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092116 | TTACAGACATGAGTC[A/G]CTGCACCTGGCCGAG | 6045 |
rs760077480 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093614 | ATATTGCTCTTATCA[A/G]TGTTATTAGTGATCT | 6045 |
rs760101501 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | RNF2 | GRCh38.p7 | 1:185098256 | GCAGCAATGGCAATT[A/G]ATCCAGTAATGGATG | 6045 |
rs760126676 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066580 | TGTCTGCCTCAGTAG[C/G]CAATACATTGTTAGA | 6045 |
rs760187494 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080560 | ATCAACTGCTGTACT[A/G]TCTGGTAAGGTAGCA | 6045 |
rs760345257 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092463 | TACAGGCGTGAGCCA[C/T]CGTGCCTAGCCGAGA | 6045 |
rs760444056 | snp | A/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102831 | ACTGCAGTGAACATT[A/T]TTATAGAAGTATATA | 6045 |
rs760462140 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087265 | CCAAGATCATGGCAC[C/T]AGCAGATGCAGTGTC | 6045 |
rs760488810 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052810 | GCAAATATCAGCTGG[G/T]GATGCTGAAGGAAGG | 6045 |
rs760581568 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074748 | TCATTATTCTCTAAA[C/T]AATACCATATAACAA | 6045 |
rs760643796 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075108 | CAAGCCATTCTCCTG[A/C]CTTAGCCTCCCTAGT | 6045 |
rs760654690 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052070 | TCCTCTTCCCTCACC[A/T]GTGACACCCCCCATT | 6045 |
rs760676860 | snp | C/G/T | 3.62058e-05 | 0.00425463 | intron-variant | RNF2 | GRCh38.p7 | 1:185099756 | TCTCATTGGCATATT[C/G/T]TAGAAATGAAATTTT | 6045 |
rs760739378 | in-del | -/GAA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056164 | AGTTCTCCATTACTT[-/GAA]GAGTTCTCCATTACT | 6045 |
rs760808554 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075357 | GATTCAACCATTTTC[C/T]ATTTCAAGAAATACA | 6045 |
rs760817375 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046680 | AAAAGGATATACATA[G/T]GCACTCAGTATTTTA | 6045 |
rs760823947 | snp | C/T | 1.65605e-05 | 0.0028775 | intron-variant | RNF2 | GRCh38.p7 | 1:185093054 | GCTTTCCCCTCCTTT[C/T]ATTTAGCAACAAAGA | 6045 |
rs760848262 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097689 | TAGGTGCACCACCAC[A/G]CCCAGCTAATTAAAA | 6045 |
rs761013288 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048886 | CTTTGAGCACTGCGT[G/T]AAGTAGTTAGCTTGC | 6045 |
rs761025181 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082733 | GCAGTGTCGATGTTG[C/T]GAGTAGTCTCCACTG | 6045 |
rs761109202 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084162 | TTGCCCAGAATGGTC[C/T]TGAACTCCTGGCCTC | 6045 |
rs761177041 | snp | A/G | 1.65633e-05 | 0.00287774 | missense | RNF2 | GRCh38.p7 | 1:185100233 | TCTTTGGAATTGGTC[A/G]GTGAGAAATACTGGA | 6045 |
rs761231018 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077983 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 6045 |
rs761259677 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048766 | AAAATCACATGTAGT[-/A]AAAAAAAAAAATCAT | 6045 |
rs761305869 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062820 | GACCTCCCCCCCCCC[-/A]AAAAAAAGGCCAATA | 6045 |
rs761541985 | snp | C/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102665 | TTAGGTGCCTCATGG[C/T]ACCTGTGGAATCACA | 6045 |
rs761607217 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075746 | GAGAACAGCAAGGGG[-/G]AAATCCACTCCCATG | 6045 |
rs761608787 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100850 | TTTTCTTCCATAATA[C/T]CTCATTTTAAAAAGA | 6045 |
rs761615546 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055044 | TTGTATCTTGAGAGA[A/G]CACCCCAAAAGTTTC | 6045 |
rs761668609 | snp | A/G | 3.30404e-05 | 0.00406437 | intron-variant | RNF2 | GRCh38.p7 | 1:185098067 | CTTTTTTCCCCCTTG[A/G]CTAGACTGCAGCGAG | 6045 |
rs761691661 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082535 | TTTTATTTTTTTTTT[-/A]GTAGAGACAGGGTTT | 6045 |
rs761718256 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051212 | TTTACACTGTTTGCT[A/G]TATAGAGTCTTATTC | 6045 |
rs761766133 | snp | G/T | 4.94311e-05 | 0.00497123 | missense | RNF2 | GRCh38.p7 | 1:185098250 | AACAATGCAGCAATG[G/T]CAATTGATCCAGTAA | 6045 |
rs761787869 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087059 | GTGTAAAGATTTTGA[A/G]TTTTTCTTCTTTTTA | 6045 |
rs761930070 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061532 | CTCATTGTTTCAAAT[A/G]CATATGCAATTATGG | 6045 |
rs761964213 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059344 | TGTTCTTGGCTATTT[G/T]TGCCTTAAAACTGCT | 6045 |
rs762075235 | snp | A/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044836 | ATGATTACATCTATT[A/C]ATCTATTACTTCGTA | 6045 |
rs762131928 | snp | C/T | 1.67525e-05 | 0.00289413 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100203 | TTTTTGTTTTAGGTA[C/T]TAAATGGCTCTTTTT | 6045 |
rs762174061 | in-del | -/TA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080934 | TCCTAGGGTCACAGT[-/TA]TACAGGTTGGGACAT | 6045 |
rs762221893 | snp | G/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044594 | CACATTGGAGGCTAT[G/T]AACCTAGTTTGCCCA | 6045 |
rs762311734 | in-del | -/GATT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047892 | AATGGTTAATTTCTC[-/GATT]GATTCATTTATTTGA | 6045 |
rs762334914 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070495 | CTTGGGAACAAATGT[A/G]TGGCCCAGTCAGAGG | 6045 |
rs762416133 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054482 | GCCTTCTTCTCCCAT[C/T]TGGGTCTCTGGCCCC | 6045 |
rs762435475 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085338 | TATTTTTAGTAGAGA[C/G]GGGGTTTCACCGTGG | 6045 |
rs762484501 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100435 | AGCCAGACTAGTTTA[C/T]GCTATTCAAATCTTT | 6045 |
rs762628231 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048275 | TCCAGTTTTATGTTG[C/T]GTGGAGCAACTCCGG | 6045 |
rs762703518 | snp | C/T | 6.69142e-05 | 0.00578383 | intron-variant | RNF2 | GRCh38.p7 | 1:185098053 | AAATTTTATGCATCC[C/T]TTTTTCCCCCTTGAC | 6045 |
rs762734800 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049366 | TGTTTGGAATAACTT[C/G]CACTTTTAAAATTAT | 6045 |
rs762741830 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075696 | AGATACTAGACACTT[A/C]TAAACAATCAGCTCT | 6045 |
rs762748743 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084462 | ATAATGTTAGATGCA[G/T]AAGGAGGACACGTTT | 6045 |
rs762797096 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055513 | GCAGCCTCCGCCTCC[C/T]AGGTTCAAGCTATTC | 6045 |
rs762828197 | snp | A/G | 1.65241e-05 | 0.00287433 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093115 | CAAAAGATCACTAAG[A/G]CCAGACCCAAACTTT | 6045 |
rs762853090 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064925 | TTTGTTTTTTTCTTG[A/C]AACGTTGCTGAATTC | 6045 |
rs763004059 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102482 | AAGGCATGTAATTCA[G/T]TGGGGTTAGGTACAT | 6045 |
rs763004286 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085505 | TCCGTCTCTGTGTCC[A/G]TGTTTAATTGCTTTA | 6045 |
rs763022675 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086587 | TGGGATATGATACCA[C/T]TTTCCAAATATTTGA | 6045 |
rs763055792 | snp | G/T | 4.94662e-05 | 0.00497299 | intron-variant | RNF2 | GRCh38.p7 | 1:185087667 | GATGACTGCCAAGGG[G/T]CATATGAGACGTGTA | 6045 |
rs763068606 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064549 | CTTAAATTGAAAACA[C/T]TGAAAGTTGAAAACA | 6045 |
rs763071849 | in-del | -/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045375 | CGGCGGCGCACCCTC[-/C]CCTCGCGCCGCGGGC | 6045 |
rs763224104 | snp | A/G | 1.65499e-05 | 0.00287657 | missense | RNF2 | GRCh38.p7 | 1:185099810 | ATAAAGACTTCTGGT[A/G]ACGCCACTGTTGATC | 6045 |
rs763242580 | in-del | -/TAAGA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064609 | GTTTCACTTTAGACT[-/TAAGA]TATTTTCAATTTTTG | 6045 |
rs763357211 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185102114 | ACTATAAGCTTTGTG[C/T]TTAGAGAATGTATGT | 6045 |
rs763431163 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060254 | TTAGTTGTGTTTCAC[A/G]TATCCCTCACAAAGA | 6045 |
rs763516235 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044573 | TCTACGTAAGTCACA[C/T]AGACACACATTGGAG | 6045 |
rs763606711 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090045 | TCCTGCTTCAGCCTC[C/T]CAAGTAGCTGGGATT | 6045 |
rs763609823 | snp | A/G | 1.64743e-05 | 0.00287 | missense | RNF2 | GRCh38.p7 | 1:185091648 | GAATTAATGTGCCCA[A/G]TTTGTTTGGATATGT | 6045 |
rs763708258 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077552 | AGAGTTGAAGATAAC[A/G]TTCTCTGACTTAATT | 6045 |
rs763801562 | in-del | -/AT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051812 | CACCAATTTTTACAT[-/AT]ATATACACACATTTT | 6045 |
rs763911063 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064929 | TTTTTTTCTTGCAAC[A/G]TTGCTGAATTCATTT | 6045 |
rs763930123 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098416 | AAAAGGCAGTCTTGT[A/G]TAAGAAGTAGGAGCA | 6045 |
rs763942290 | snp | C/T | 1.65894e-05 | 0.00288 | intron-variant | RNF2 | GRCh38.p7 | 1:185098060 | ATGCATCCTTTTTTC[C/T]CCCTTGACTAGACTG | 6045 |
rs763984956 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052226 | TCCTACCACTAAACC[A/G]GAGGTATCCAAAGTA | 6045 |
rs764017892 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084521 | CTTCTTACTTTTGCA[A/C]GAGAATCTTCTAGGG | 6045 |
rs764035888 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055898 | GGGCTCTTTGAATTA[C/G]TGCAAAAGTGCTTTT | 6045 |
rs764045210 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078529 | CCCTAGTTTAACTCA[C/T]AAAGTATCAGCATTA | 6045 |
rs764086088 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053725 | AATTACTGTTGATTT[C/T]CCAATATCCAAAACA | 6045 |
rs764196928 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076680 | TGAAAAGGGTTTAAA[A/T]TTTTTTTTTGTCATC | 6045 |
rs764279009 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085065 | GTACTGCTCTTCCAA[C/T]GCATACTTTTCTTTC | 6045 |
rs764334110 | snp | A/C | 4.948e-05 | 0.00497369 | intron-variant | RNF2 | GRCh38.p7 | 1:185087674 | GCCAAGGGGCATATG[A/C]GACGTGTAAACTGGG | 6045 |
rs764387219 | snp | C/T | 1.65004e-05 | 0.00287227 | intron-variant | RNF2 | GRCh38.p7 | 1:185087539 | ATTGTTTTTCTCTCT[C/T]CTTTATTTCCAGCAA | 6045 |
rs764403045 | in-del | -/TTT | 1.64972e-05 | 0.00287199 | intron-variant | RNF2 | GRCh38.p7 | 1:185087541 | TGTTTTTCTCTCTTC[-/TTT]ATTTCCAGCAATGTC | 6045 |
rs764422181 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058130 | TACCCCATCTCAGAT[A/G]ATAATAGTAATACAA | 6045 |
rs764442746 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059118 | GTTGCAAGTTGCAGA[A/T]ATCTGGCGACAAGGC | 6045 |
rs764475742 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080883 | ATTTTCCAGGGTAGC[A/G]TTCAGTAGGCAGAAG | 6045 |
rs764560905 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044693 | CTTCTCAAGAGAACA[C/T]GACATCTCAACAATA | 6045 |
rs764561414 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065874 | CTGTTTCCTTTTTTT[-/C]CCCCCTACTTGCTCT | 6045 |
rs764575823 | snp | C/T | 6.61835e-05 | 0.00575216 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185099812 | AAAGACTTCTGGTAA[C/T]GCCACTGTTGATCAC | 6045 |
rs764641936 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067894 | TTTTGTATTTTTAAT[A/G]CAGATGGGGTTTCAC | 6045 |
rs764660466 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185069197 | GTGGCTCATGCCTGT[A/G]ATCCCAGCACTTTGC | 6045 |
rs764749131 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070399 | TTTGTTGTTTTATAA[C/T]ATAAAGGGATCCCTA | 6045 |
rs764865002 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044777 | ATTTATATGCATTAA[A/G]TGTCGGATAATTTAC | 6045 |
rs764900784 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061022 | CTTGGGAGGCTGACA[C/T]GGGAGGATCGCTTGA | 6045 |
rs764961469 | snp | A/G | 1.70362e-05 | 0.00291853 | intron-variant | RNF2 | GRCh38.p7 | 1:185099777 | ATGAAATTTTTAATG[A/G]TTTATTCTTCTAGAT | 6045 |
rs764981788 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088949 | CATGCAAATGAGGTG[A/C]TGAATGGGCATTGTA | 6045 |
rs764998136 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089953 | TTGAGACAGAGTATC[C/G]CTCTGTCACCTAGGC | 6045 |
rs765003126 | snp | C/T | 3.31027e-05 | 0.0040682 | intron-variant | RNF2 | GRCh38.p7 | 1:185091761 | TGAAAAGAGTTGTTA[C/T]ACTAGGTACTTAATT | 6045 |
rs765013073 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079258 | TATAATTAATGAGCT[A/G]TAACTGGAAATTGGG | 6045 |
rs765018008 | snp | A/G | 1.65589e-05 | 0.00287736 | intron-variant | RNF2 | GRCh38.p7 | 1:185093055 | CTTTCCCCTCCTTTT[A/G]TTTAGCAACAAAGAA | 6045 |
rs765097591 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065345 | GGCAGGGCCAAATAA[-/G]GGGAATAAAAGCTGG | 6045 |
rs765147865 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097097 | AACTGGAGGCAAATT[A/G]TTTAATCTTGTACCT | 6045 |
rs765154471 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064806 | GCCTCCTTGGCTTAA[A/G]TTTATTCCTAAGCAT | 6045 |
rs765183115 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049096 | CCAGGCATAGTGGCG[C/T]GCGCCTGTAATCCCA | 6045 |
rs765187113 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084316 | TCAGCATTGTAGCAA[C/T]TTTAAATGAGTATTA | 6045 |
rs765200035 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063235 | TTTTTACACAGAATA[C/T]GTAGAATAGTGGTTC | 6045 |
rs765259447 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047370 | AATACTGGGAATTTG[A/G]AGTTTTTCTCTGCCT | 6045 |
rs765261190 | snp | A/C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055366 | TTATTGGGGTGATAA[A/C/G]CCTGTATCGTTTATT | 6045 |
rs765301806 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083911 | TGTGCCTGGCCTACC[-/T]TTTTTTTTTTTTTTT | 6045 |
rs765346876 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070849 | CACCGTATTAGCCGG[C/G]ATGGTCTCGATTTCC | 6045 |
rs765410367 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058534 | GGAAAACTGTAAAAA[A/G]TATTTGAAACAGTAT | 6045 |
rs765457797 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061780 | TTCTTAGCTCAGGAG[A/G]ACAAGACTGTTTTTA | 6045 |
rs765469757 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085474 | GTTTTGTATATCATT[C/T]AGTGCTCTCTCTAAT | 6045 |
rs765528629 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047981 | CCCATATAATTTGGG[G/T]TACAAAGGTATAATA | 6045 |
rs765555655 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185071858 | GGTTTCTTGATATGC[C/T]GAAGGAATATTAGGC | 6045 |
rs765614836 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056157 | TTTCAGGAGTTCTCC[A/G]TTACTTGAAGAGTTC | 6045 |
rs765658055 | snp | G/T | 6.59478e-05 | 0.00574191 | missense | RNF2 | GRCh38.p7 | 1:185098300 | TGAATTAGTATTCAG[G/T]CCTCATCCCACACTT | 6045 |
rs765696440 | snp | A/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101867 | TTTGTAATCTGTGCC[A/T]TGAAATTTGAAAACC | 6045 |
rs765864785 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045082 | CATGTGAAGTTCTGC[A/G]AACCAAAGCCTGATG | 6045 |
rs765954665 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087371 | TCTTTTATAAAGGCA[C/T]TAATTTCATTCATGA | 6045 |
rs765979968 | in-del | -/AAAGAT | 1.69703e-05 | 0.00291288 | intron-variant | RNF2 | GRCh38.p7 | 1:185093014 | TTTTGTCTTTAGCCC[-/AAAGAT]ACTAGCATTGTTTAC | 6045 |
rs765982397 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070854 | TATTAGCCGGGATGG[A/T]CTCGATTTCCTGACC | 6045 |
rs765982546 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100494 | AAGGGACTGCAATTA[C/T]TCAGTATTTTTTTCT | 6045 |
rs766014374 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052879 | GCCTCAAGTAATGAC[A/G]GTGATAATAAGAGAT | 6045 |
rs766047000 | snp | A/C | 1.6477e-05 | 0.00287024 | missense | RNF2 | GRCh38.p7 | 1:185098259 | GCAATGGCAATTGAT[A/C]CAGTAATGGATGGTG | 6045 |
rs766104142 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | RNF2 | GRCh38.p7 | 1:185098109 | CAGATTGAAAATGGT[A/G]GTGGAGCAGAAGATA | 6045 |
rs766107729 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057801 | GAAAATTACTCTAAA[-/G]GGGGAAAAAAAAAAA | 6045 |
rs766304761 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062946 | GGTTTTTTAAAAAAA[A/T]GTTGCTCTTCCCTAA | 6045 |
rs766312174 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074775 | ACAATTATTTACATA[A/G]CGTTTACATTGTATT | 6045 |
rs766319389 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097050 | GGTCTGGTTCACATC[C/T]TAGCTCTAGTTCTGG | 6045 |
rs766331451 | in-del | -/ATTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083361 | CAATTTTCCATTTTA[-/ATTTT]ATTTTATAAGTCCCG | 6045 |
rs766333497 | snp | A/G | 1.65397e-05 | 0.00287569 | missense | RNF2 | GRCh38.p7 | 1:185100243 | TGGTCAGTGAGAAAT[A/G]CTGGAAAGTGAACAA | 6045 |
rs766358222 | in-del | -/GA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073563 | AGCAGTTAATTTTTT[-/GA]GTTTTTTAAAAGGAC | 6045 |
rs766358697 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097289 | TATTTAGATACCATC[A/G]CATTTTCCTCAGTCA | 6045 |
rs766388928 | in-del | -/TTT | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101834 | TGTTTTTACAGGGTT[-/TTT]TTTTTTTTTTTTTTT | 6045 |
rs766404333 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045129 | GGGACAGGTTTAAGA[A/G]GACGAACTCATGAGA | 6045 |
rs766457888 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047115 | CTCCTTTTTCTAGGG[A/G]TAGCACAGCAAATAT | 6045 |
rs766497806 | snp | A/T | 1.67284e-05 | 0.00289205 | intron-variant | RNF2 | GRCh38.p7 | 1:185100005 | AAACTGGGAGCACAC[A/T]GACCAACTAACTGAG | 6045 |
rs766531909 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076522 | CGATCTCCTGACCTT[A/G]TGATCCACCTGCCTT | 6045 |
rs766706777 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082789 | TAAGAAAATCACTCA[A/T]ATTTGTTTTTTGTCT | 6045 |
rs766723311 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084176 | CTTGAACTCCTGGCC[C/T]CAGGCAGTCCTGTGA | 6045 |
rs766725188 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069620 | TGTAGATTCTGTATA[C/T]TTTAGCCCTATACTC | 6045 |
rs766804825 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087710 | TTTTTAGAACATGAA[A/C]ACTTAAATAGAACAT | 6045 |
rs766814121 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070796 | GGTGCCCGCCACCTC[G/T]CCGGCTCATTTTTTT | 6045 |
rs766864421 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048656 | CAAAAGATATGTTAC[C/T]TACGGGCTCTTCTGC | 6045 |
rs766866892 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090205 | AATTACAGGTGTGAG[C/T]CATCGTGCCTGGCCG | 6045 |
rs766939863 | in-del | -/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100547 | AGTTTCTTGTGTTTT[-/T]TTTTTTTCCCCACAA | 6045 |
rs766943215 | in-del | -/AAC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062474 | GAGAAGAGAGAACTA[-/AAC]AATGATGTTGGGAAA | 6045 |
rs766992965 | snp | A/G | 1.65542e-05 | 0.00287695 | missense | RNF2 | GRCh38.p7 | 1:185093162 | AAATTTATCCAAGTC[A/G]TGATGAGTATGAAGC | 6045 |
rs767010939 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078006 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGCCAGCG | 6045 |
rs767048284 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078874 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAATAC | 6045 |
rs767079080 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100896 | TAGTGTCCATTGTCA[C/T]GCAATGTTTTTTTTT | 6045 |
rs767082110 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051315 | TATTGTGTATAGTAG[A/G]AGTTGCAGAATTGAA | 6045 |
rs767097981 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088250 | GCTGTTTCAACATTT[A/C]GAAATTAGGTAATGG | 6045 |
rs767172535 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065227 | TCTAAAAATGCACCA[A/G]TCAGTGCTCTGTGTC | 6045 |
rs767252871 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101488 | AACAATATTGGGTGT[C/T]TGGGAGCCAGAAAGC | 6045 |
rs767266248 | in-del | -/ACT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095583 | CCTAAGAGGGAAGAG[-/ACT]ACTATGTCAGTATCA | 6045 |
rs767357999 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051308 | GGGGTAGTATTGTGT[A/G]TAGTAGGAGTTGCAG | 6045 |
rs767360873 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101349 | GGCGCTCTTTTAATT[-/A]ACACTCTGTAGAAGG | 6045 |
rs767456664 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087177 | TAATCCATTTAGCCT[A/G]CTATAAAAAATACTT | 6045 |
rs767498417 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073647 | TATTATACTGTGGTT[C/G]TAAGGGCTGATGTGT | 6045 |
rs767509369 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072597 | GACTAGCTAGTGGAA[A/G]GACTCTAAAATGAGA | 6045 |
rs767514824 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059372 | GCTAAAAATCTGTGC[A/C]TTATTGTAATATGGT | 6045 |
rs767516686 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074709 | ATGGTTGCATCTGAA[C/T]GTGTACAGATTTTTT | 6045 |
rs767532566 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079576 | CCTCCTCTCCTCTCA[C/T]TGGAACAGTCATTTT | 6045 |
rs767562361 | in-del | -/AAGTG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048587 | TGAGAGCATACTATT[-/AAGTG]AAGTAACCAGCCAAA | 6045 |
rs767726526 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082726 | GTGGAATGCAGTGTC[A/G]ATGTTGCGAGTAGTC | 6045 |
rs767761145 | snp | A/G | 1.6517e-05 | 0.00287372 | missense | RNF2 | GRCh38.p7 | 1:185091736 | TCACAGCCCTTAGAA[A/G]TGGGTATGTTGAAAA | 6045 |
rs767776701 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054287 | AAAACGAACCCCCAG[G/T]TTACAGGTAAGGAAA | 6045 |
rs767794078 | in-del | -/A | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102576 | ACTCTGTGTGCAATT[-/A]AAAGTAATGCATTTC | 6045 |
rs767816541 | snp | A/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044837 | TGATTACATCTATTA[A/C]TCTATTACTTCGTAA | 6045 |
rs767844996 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095350 | CAGACTCACCAAGCA[C/T]GCTTCTGCCTCAGAG | 6045 |
rs767863646 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096631 | TAGGCCACCAAGTTA[C/T]GTATTTGTACTTTTG | 6045 |
rs767882323 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068269 | TTATAGTCACTCTTA[C/G]TTTGGTCAGTGTGGT | 6045 |
rs767884777 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069593 | GAGAGTCTGACCAAA[A/G]AGTAAAGGCCATGTA | 6045 |
rs767985624 | snp | C/T | 1.6643e-05 | 0.00288465 | intron-variant | RNF2 | GRCh38.p7 | 1:185099988 | AAAATAATAGACTGT[C/T]GAAACTGGGAGCACA | 6045 |
rs767987160 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071490 | AAGTAGTATTGCCTT[A/G]CTTAGTTCCTAAGCT | 6045 |
rs767991362 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052981 | AATCCTTAAGAACTC[-/T]TAAGAGGTGGTATGA | 6045 |
rs768087382 | snp | C/T | 8.49322e-05 | 0.00651605 | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100325 | AAACCAATTCTGAGA[C/T]TGAACTTTTTTATAG | 6045 |
rs768269010 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094351 | GTTTCACCATATTGG[C/T]GAGGCTGGTCTCAAC | 6045 |
rs768270780 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084087 | CTAAAACTACAGGCA[-/C]CACACCATCACACCC | 6045 |
rs768356678 | in-del | -/TT | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101833 | TCTGTTTTTACAGGG[-/TT]TTTTTTTTTTTTTTT | 6045 |
rs768356894 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185079884 | GCAGTGAGCTGAGAT[C/T]GCGCCACTGCACTCT | 6045 |
rs768376906 | snp | A/T | 0.000101211 | 0.00711304 | splice-acceptor-variant | RNF2 | GRCh38.p7 | 1:185100198 | TTTCTTTTTTGTTTT[A/T]GGTATTAAATGGCTC | 6045 |
rs768385368 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057051 | CGGTGGCTCATGCCT[A/G]TAATCCAGTACTTTG | 6045 |
rs768397503 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058338 | CGGGGTATCTTCAGA[A/T]CCCCATGGATACTCA | 6045 |
rs768411534 | snp | C/T | 1.65351e-05 | 0.00287528 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185093139 | AAACTTTGATGCACT[C/T]ATCAGCAAAATTTAT | 6045 |
rs768430145 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078675 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA | 6045 |
rs768483949 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081242 | CATGCTTTGGGATTC[C/G]ATGAACTCTTGGAAA | 6045 |
rs768588472 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089751 | GATGGAGATAGAGGC[C/T]GGGCGTGGTGGCTCA | 6045 |
rs768591049 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102546 | TTGTAAAACTTTTTC[A/G]TCACCCCAAACAGAA | 6045 |
rs768648029 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185069457 | AGTGAGACCCTGTCT[-/A]AAAAAAAAAAAAAAA | 6045 |
rs768654645 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049836 | GTTCTGGGAGAACCA[C/G]AAAAACCTGGAGACT | 6045 |
rs768678757 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086659 | TAGTTTGTCTTCAGA[C/G]GGCAGCTATAGGATG | 6045 |
rs768753489 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061387 | AAAAAAAAAGGGAAA[C/T]AGAAATGAAAGCTTC | 6045 |
rs768795162 | snp | C/T | 3.29478e-05 | 0.00405867 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185091653 | AATGTGCCCAATTTG[C/T]TTGGATATGTTGAAG | 6045 |
rs768839724 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052664 | GCTAAATGCCACTAA[A/G]TGTTCAATTTAAAAT | 6045 |
rs768841535 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060307 | TTAAGTCTACAGGTT[C/T]ATTTATTGGGGCCAG | 6045 |
rs768844278 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088317 | AGAGAAAAGGAAGGA[A/C]AAACAGGAGATTGAG | 6045 |
rs768867563 | in-del | -/CGCTCTGACGC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061158 | TTTGAGACGGAATCT[-/CGCTCTGACGC]CCAGGCTGGAGTGCA | 6045 |
rs768928450 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074325 | CTGGATCTCCAAACT[C/T]TTTTCCCTCTTTAGT | 6045 |
rs768929485 | in-del | -/GTGT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049344 | CATTAAAGGAGGTGA[-/GTGT]GTGTGTTTGGAATAA | 6045 |
rs768932583 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089511 | TCACCTGAGTAGATT[A/G]TACAAGTTTGAGGGT | 6045 |
rs768948668 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075218 | AGGCTGGTTTCGAAC[A/T]TCTGACCTCAGGTGA | 6045 |
rs769063864 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095527 | TTTCCCATAGCACGT[A/G]TCACTCTCTCATGTG | 6045 |
rs769092224 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062552 | CATGTAAAAAAAAAT[A/T]GCAAGAAAGTATAGG | 6045 |
rs769098807 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097551 | AAAGAAAATTATTTT[C/T]AAGAGATAGCGTCTT | 6045 |
rs769115152 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083548 | TGCAGCCTTGAACTC[C/G]TGGGCTCAAGCAGTC | 6045 |
rs769127464 | snp | C/T | 1.82105e-05 | 0.00301743 | intron-variant | RNF2 | GRCh38.p7 | 1:185100176 | GTGCAGTTTTCATAA[C/T]TTTTTCTTTCTTTTT | 6045 |
rs769171888 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096298 | CTTAACCATTTGTAA[A/G]TGTAGAGTTCAGTAG | 6045 |
rs769268026 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046386 | CCGTGTCGTTTACGC[G/T]GAGATGCTAGTACCC | 6045 |
rs769314033 | snp | C/T | 1.69729e-05 | 0.0029131 | intron-variant | RNF2 | GRCh38.p7 | 1:185093012 | ATTTTTGTCTTTAGC[C/T]CAAAGATACTAGCAT | 6045 |
rs769316429 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070428 | TAAAATAGTTCTCTG[C/T]CTTTACTTTGGGGAA | 6045 |
rs769440055 | snp | A/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100356 | CCTATTTCTTTAATA[A/T]TAAAGATGTACTGGC | 6045 |
rs769560921 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057186 | TGTGGTGGTGCACAC[A/C]TGTAGTCCCAGTTAC | 6045 |
rs769670085 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091055 | TTAAAATGAAATTCT[A/G]TTAAGCTGTTTATAA | 6045 |
rs769708042 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057634 | GAATGAAAGAAGATA[A/G]CCTGTTTCCCCATTT | 6045 |
rs769727724 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065941 | AAAAATACTACTTTC[-/T]TGCTATACTGTCTCA | 6045 |
rs769830556 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092620 | TGAGGAAATTACAAC[A/G]CATAAAACCACGATT | 6045 |
rs769914773 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078480 | TTGGTTTCCCTATCT[C/T]ACATGGCTCCTCTTC | 6045 |
rs769923336 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050682 | AATAGTTTGGGTAAA[G/T]TGTTACTTGATTTTA | 6045 |
rs769956863 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052528 | AGAAAAATCCATAGA[C/T]TGGTGGTTGCCAGAG | 6045 |
rs769971214 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086446 | GTTGGTCTTATGCTC[C/T]TCAGTTCATTTATAT | 6045 |
rs769985354 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072854 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCACGAG | 6045 |
rs770050316 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089609 | TATATGGCCCAGTAA[A/G]GGGAGGGTAGAAGTG | 6045 |
rs770094200 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091635 | AAGTCTACACAGTGA[A/G]TTAATGTGCCCAATT | 6045 |
rs770152890 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066251 | CTAGGCCTCACTGAT[A/C]TAGTTCACATTTAAA | 6045 |
rs770215480 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074187 | AGGAGCTCCTGTCCT[G/T]TGGAGTTAGAGTGTA | 6045 |
rs770304050 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058682 | GTGTTATGGTTTTCT[C/G]TTTTTAATATTGATT | 6045 |
rs770311201 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096097 | AAAATAAATATATTG[A/G]GTCTTAATAAACCTG | 6045 |
rs770350329 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094821 | CATTATCGTCTGATT[C/T]ATTCAGGCCTCAAGG | 6045 |
rs770354678 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | RNF2 | GRCh38.p7 | 1:185087660 | TGACTAAGATGACTG[C/T]CAAGGGGCATATGAG | 6045 |
rs770463426 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059997 | TGTTAGTATATTTCC[A/G]TTGACACAAGGGAAT | 6045 |
rs770543252 | snp | G/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044086 | CTTGGGCTCCCAAAG[G/T]GCTGAGATTACAGGC | 6045 |
rs770551755 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082267 | AGCTTCTATGATTGT[A/C]CTCAGTTGGTCGTTG | 6045 |
rs770582185 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076596 | GGCCTTATTTTATGG[-/T]TTTTTTTTTTTATGT | 6045 |
rs770602645 | snp | C/T | 1.66551e-05 | 0.00288571 | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091572 | TTTTAAAGTGACTCT[C/T]TTACAGGAGGCAATA | 6045 |
rs770606084 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050941 | TTTCAGTTCCCAAAA[A/G]TAAAACATTATGTAG | 6045 |
rs770639406 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068998 | CCTTTTTTGAGTAAA[A/G]TGTTTCATCCAATTT | 6045 |
rs770653953 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070079 | GCTAAATAATTTTCT[C/G]CCTGGTCTTTTACAT | 6045 |
rs770662686 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055337 | TGTCCATGTCCAAAA[A/T]GTTTTAGATTTTCTT | 6045 |
rs770832126 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075446 | ACTTTGCCAATGGTT[C/T]GACAATTCCTGTTTC | 6045 |
rs770872637 | snp | C/G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185063647 | TACTATTTTACAGTT[C/G/T]TGGCAGTAAGAAGTC | 6045 |
rs770880570 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057224 | GCTGATGTGGGAGGA[-/T]TGCTTGAACCCAGGA | 6045 |
rs770969401 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094961 | CTTTAGGCATCATCC[C/T]GGTCCCAGTAATCAG | 6045 |
rs771015355 | snp | A/G | 1.65162e-05 | 0.00287365 | missense | RNF2 | GRCh38.p7 | 1:185099951 | ATAGCAACAGCCAGT[A/G]GCCAGTTCACTGTGA | 6045 |
rs771065722 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064464 | ATTTTTCAACTTTAC[A/G]GTGGTACAAAAGCAA | 6045 |
rs771073687 | snp | A/G/T | 1.67091e-05 | 0.00289038 | intron-variant | RNF2 | GRCh38.p7 | 1:185100001 | GTTGAAACTGGGAGC[A/G/T]CACTGACCAACTAAC | 6045 |
rs771083534 | snp | G/T | 1.6945e-05 | 0.00291071 | intron-variant | RNF2 | GRCh38.p7 | 1:185098036 | TTTAAAGGCCTAAAA[G/T]TAAATTTTATGCATC | 6045 |
rs771084261 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098204 | CAAACGGACCAAAAC[A/G]TCTGATGATTCTGGG | 6045 |
rs771099977 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065986 | GTATCAGCATCTACA[C/T]AGCCACAAGCTTAGG | 6045 |
rs771230269 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087628 | TTTATATGAGTTACA[A/G]CGAACACCTCAGGTA | 6045 |
rs771263184 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050472 | TGAGATGTCTCAATT[G/T]CGTCACATAATTATT | 6045 |
rs771383005 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085255 | CCGGGTTCATGCTAT[C/T]CTCCTGCCTCAGCCT | 6045 |
rs771450237 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086221 | CTTAGACTTTGTCTT[A/G]TCGATTGTTGTTTAT | 6045 |
rs771472685 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092059 | ATATTGAACTCCTGA[A/C]CTCAGGTAATCCACC | 6045 |
rs771546544 | snp | C/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071645 | CCCGCCAATCTTGGA[C/G]AAGTTGAACATGGTC | 6045 |
rs771602504 | in-del | -/CCTA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050353 | CTTGCCTCTTCTCTG[-/CCTA]CCTAACTTTATAACT | 6045 |
rs771612763 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087589 | AAACGGAACTCAACC[A/G]TTAAGCAAAACATGG | 6045 |
rs771684079 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094461 | GTCGCTTTTAAATCT[C/G]TTTTACACATCCTGT | 6045 |
rs771697106 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082008 | GTCCAACCACTGAGC[A/G]GGTCGTCACTAGTTA | 6045 |
rs771717949 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080498 | ATAAGAATTGAGATA[A/G]TGATTTTGGCAGTCT | 6045 |
rs771729724 | in-del | -/AA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057806 | ATTACTCTAAAGGGG[-/AA]AAAAAAAAAAAACAG | 6045 |
rs771761349 | in-del | -/ATT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077836 | TGTTTTTTTTCAGTC[-/ATT]ATTGTTTTATTATTT | 6045 |
rs771788985 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068795 | TAAATGGACATTTCT[A/G]AGTAACTCAGTTTAC | 6045 |
rs771814032 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043882 | TGGAGTGTCATGGCG[C/G]GATCTCGGCTCACTG | 6045 |
rs771816017 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080436 | TATATTGATCTAAAG[A/C]AAAGAGACACTAATT | 6045 |
rs771887976 | in-del | -/TTC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053517 | TCTTATTTTCTTTCT[-/TTC]TTTTTTCTTTATTTT | 6045 |
rs771923703 | snp | A/G | 1.6477e-05 | 0.00287024 | missense | RNF2 | GRCh38.p7 | 1:185098253 | AATGCAGCAATGGCA[A/G]TTGATCCAGTAATGG | 6045 |
rs771960370 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088587 | TAAAGGAAGTATTTC[A/G]AGGAGGATGTAGTTA | 6045 |
rs771992005 | in-del | -/TTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077399 | CATTTTGCTCCTGAC[-/TTT]TTTAACAGGAATGTG | 6045 |
rs772092735 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091082 | ATAAACTAGAGAAAC[-/TT]TTATTGGAATCTTGT | 6045 |
rs772114070 | snp | A/G | 1.68488e-05 | 0.00290243 | intron-variant | RNF2 | GRCh38.p7 | 1:185093026 | CCCAAAGATACTAGC[A/G]TTGTTTACATTTGCT | 6045 |
rs772136635 | snp | A/G | 5.10573e-05 | 0.00505233 | intron-variant | RNF2 | GRCh38.p7 | 1:185098024 | CAGATTTGTTGCTTT[A/G]AAGGCCTAAAAGTAA | 6045 |
rs772153160 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089659 | TTCTTCAGAGAAATT[C/T]AGCTATGCAGGGGAG | 6045 |
rs772252627 | in-del | -/ACT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095378 | AGCCTTTGTACTTAC[-/ACT]ACTACTCTATTTCAG | 6045 |
rs772266380 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055019 | TTTTCACCAAGGTTG[C/T]ATGTGTTGATTGTAT | 6045 |
rs772488618 | snp | C/T | 1.66874e-05 | 0.0028885 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100208 | GTTTTAGGTATTAAA[C/T]GGCTCTTTTTCTTTG | 6045 |
rs772524392 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097652 | CATCCTCCTGTCTCA[C/G]CCTCCTGAGTAGCTG | 6045 |
rs772670765 | in-del | -/AG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077005 | CTTCAGTTAAGTTGT[-/AG]AGTTTTGTCTTTTCA | 6045 |
rs772676644 | in-del | -/CT | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102563 | CACCCCAAACAGAAA[-/CT]CTGTGTGCAATTAAA | 6045 |
rs772683778 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099376 | CTATGGTTAGTCTTA[A/C]AAGACATTTTAATTC | 6045 |
rs772700446 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070536 | AGCCTTGGGATCTCA[A/G]AGAGTTGAATGGGAA | 6045 |
rs772734470 | snp | A/C | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043933 | CAAGCGATTCTCCTG[A/C]CTCAGCCTCCCGAGT | 6045 |
rs772765484 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085008 | TGGACCACTCTACCT[C/T]AGTGGTCCCTGAGTA | 6045 |
rs772775082 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067502 | GAAAAGAAAAATGCT[A/G]AAGATTGAGAGAGTT | 6045 |
rs772776841 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078886 | CTCGTCTCTACTAAA[A/G]TACAAAAATTTGCCA | 6045 |
rs772794878 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080508 | AGATAATGATTTTGG[C/G]AGTCTGCAAGACTTT | 6045 |
rs772912124 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074718 | CTGAACGTGTACAGA[-/T]TTTTTTTTCTCGTGT | 6045 |
rs772969980 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055507 | CTCACTGCAGCCTCC[A/G]CCTCCCAGGTTCAAG | 6045 |
rs773012587 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084380 | AAAGGATAGTTCATT[G/T]AGGATTTTTGGGGAG | 6045 |
rs773013535 | snp | C/T | 3.63875e-05 | 0.00426526 | intron-variant | RNF2 | GRCh38.p7 | 1:185099750 | CATTTTTCTCATTGG[C/T]ATATTCTAGAAATGA | 6045 |
rs773046345 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089674 | CAGCTATGCAGGGGA[A/G]CAGAGAAATGGAGCA | 6045 |
rs773136796 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088625 | TAACACTAGTGACAG[A/G]CTTAATAAGATGAAG | 6045 |
rs773157943 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074711 | GGTTGCATCTGAACG[G/T]GTACAGATTTTTTTT | 6045 |
rs773171214 | snp | A/C | 1.70081e-05 | 0.00291612 | intron-variant | RNF2 | GRCh38.p7 | 1:185098025 | AGATTTGTTGCTTTA[A/C]AGGCCTAAAAGTAAA | 6045 |
rs773186938 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053728 | TACTGTTGATTTCCC[-/A]ATATCCAAAACAATG | 6045 |
rs773208098 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075346 | CCATATAGCTTGATT[C/G]AACCATTTTCCATTT | 6045 |
rs773247381 | snp | C/T | 1.6477e-05 | 0.00287024 | missense | RNF2 | GRCh38.p7 | 1:185098254 | ATGCAGCAATGGCAA[C/T]TGATCCAGTAATGGA | 6045 |
rs773428328 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064338 | TATTCTTCATAGAAT[A/C]CTACAGAATAGGTAC | 6045 |
rs773450870 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046661 | GTTTCTTTGAAGTGC[C/T]GTGAAAAGGATATAC | 6045 |
rs773472736 | snp | A/G | 1.67562e-05 | 0.00289444 | intron-variant | RNF2 | GRCh38.p7 | 1:185093033 | ATACTAGCATTGTTT[A/G]CATTTGCTTTCCCCT | 6045 |
rs773491109 | in-del | -/TT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085145 | CCTTCTTTCTTTTTC[-/TT]TTTTTTTTTTTTTTT | 6045 |
rs773500308 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066307 | GCTGTACTCCCCACC[A/T]TCTTTTCCACTCATT | 6045 |
rs773505843 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048817 | GGCAGAACAACATAC[C/G]AATAAGTTCAGCTAA | 6045 |
rs773590124 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097673 | TGAGTAGCTGAGATG[A/T]TAGGTGCACCACCAC | 6045 |
rs773592761 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055915 | GCAAAAGTGCTTTTT[G/T]TTAATGTAGATAGCT | 6045 |
rs773597103 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185050375 | AACTTTATAACTACT[A/C]TTTTTATCTTCTATC | 6045 |
rs773654920 | snp | C/T | 4.97533e-05 | 0.0049874 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185100227 | TCTTTTTCTTTGGAA[C/T]TGGTCAGTGAGAAAT | 6045 |
rs773749765 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084151 | TTCTTGCTATGTTGC[C/T]CAGAATGGTCTTGAA | 6045 |
rs773860699 | in-del | -/AT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051955 | TATACATTTTTACAT[-/AT]ATATATATATATATG | 6045 |
rs773915360 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087527 | CCAAATACTAAAATT[A/G]TTTTTCTCTCTTCTT | 6045 |
rs773965067 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057408 | TAGGTGTATGAACCA[C/T]AGTATATTTAATCAT | 6045 |
rs774018730 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074195 | CTGTCCTGTGGAGTT[-/A]GAGTGTATCACCCTT | 6045 |
rs774076352 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077433 | CAAAAGTTTTAACAT[A/T]GATTGTTTTGGGACT | 6045 |
rs774132988 | snp | A/G | 3.29544e-05 | 0.00405908 | missense | RNF2 | GRCh38.p7 | 1:185098247 | AATAACAATGCAGCA[A/G]TGGCAATTGATCCAG | 6045 |
rs774257752 | snp | C/T | 1.65373e-05 | 0.00287548 | intron-variant | RNF2 | GRCh38.p7 | 1:185098065 | TCCTTTTTTCCCCCT[C/T]GACTAGACTGCAGCG | 6045 |
rs774290283 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086800 | TGCTCTAAAGTAGAT[A/T]TTTTAACTTGGACAG | 6045 |
rs774373399 | in-del | -/AA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054110 | CTAGAAGTGAAACTG[-/AA]CCGGGAAAAAGGATA | 6045 |
rs774420127 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067441 | ATTGCTTTAATTAAG[G/T]AAGAAATTATTTGCT | 6045 |
rs774422139 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051099 | TTGTTTCCCACACCA[G/T]TCACACACTATGTTG | 6045 |
rs774438568 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052684 | CAATTTAAAATGGTT[C/T]ATTTCACCCCAGTAA | 6045 |
rs774454005 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088385 | AACATGGAGAAACCC[C/T]GTCTCTACTGAAAAT | 6045 |
rs774487552 | in-del | -/ATT | | | cds-indel, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101296 | TGTTTCCATTGGAAA[-/ATT]ATATCATTTTGGGTT | 6045 |
rs774517124 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068106 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 6045 |
rs774520203 | snp | C/T | 3.38244e-05 | 0.0041123 | intron-variant | RNF2 | GRCh38.p7 | 1:185093021 | TTTAGCCCAAAGATA[C/T]TAGCATTGTTTACAT | 6045 |
rs774525981 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062555 | GTAAAAAAAAATTGC[A/G]AGAAAGTATAGGTGG | 6045 |
rs774533536 | in-del | -/G | 1.65282e-05 | 0.00287469 | frameshift-variant | RNF2 | GRCh38.p7 | 1:185100253 | GAAATACTGGAAAGT[-/G]AACAAACCCATGGAA | 6045 |
rs774539153 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074452 | GAATCTATCTAGGGG[C/G]CCACCTAGAGTAACC | 6045 |
rs774596277 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076277 | ATGGGTTGTTTTTTT[-/TTTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTGAGAC | 6045 |
rs774635530 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185060355 | ATAGAGTGGCAGTCA[A/G]CAGTCAGTAGTAACC | 6045 |
rs774723549 | snp | C/T | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185044710 | ACATCTCAACAATAG[C/T]ACATATAGAGATCAG | 6045 |
rs774939360 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097569 | GAGATAGCGTCTTAC[C/T]CTGGCCCAGGCCAGA | 6045 |
rs774954292 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083634 | CTCTAGTCACTATTA[C/T]TAGGTGTATTTTTGT | 6045 |
rs775024802 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091432 | CGATTATAGTTGAAA[C/T]AAAATTAGCTGTGAG | 6045 |
rs775036470 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078029 | GGCCAGCGGATCACC[C/T]GAGGTTTGAGGTTCG | 6045 |
rs775068909 | snp | G/T | 1.82151e-05 | 0.00301782 | intron-variant | RNF2 | GRCh38.p7 | 1:185100177 | TGCAGTTTTCATAAT[G/T]TTTTCTTTCTTTTTT | 6045 |
rs775111785 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070488 | GAATGGTCTTGGGAA[A/C]AAATGTATGGCCCAG | 6045 |
rs775115003 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053634 | CTGGGATTACAGGCT[C/T]TGGCCACCACATCCA | 6045 |
rs775117428 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055589 | CCAGCTAATTTTTGT[A/G]TTTTGAGTAGAGTTG | 6045 |
rs775126926 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064302 | GCTAGTCTTATTGCA[C/T]CAATAATAATAGCTA | 6045 |
rs775133788 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057230 | GTGGGAGGATTGCTT[A/G]AACCCAGGAGTTGGA | 6045 |
rs775225104 | in-del | -/AG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080238 | ACATAGGTGACTCTC[-/AG]ATATTGTTCATTGAA | 6045 |
rs775250804 | snp | C/T | 1.65701e-05 | 0.00287833 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185099806 | ATACATAAAGACTTC[C/T]GGTAACGCCACTGTT | 6045 |
rs775503229 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085493 | GCTCTCTCTAATTCC[A/G]TCTCTGTGTCCATGT | 6045 |
rs775550908 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078483 | GTTTCCCTATCTTAC[A/G]TGGCTCCTCTTCTCC | 6045 |
rs775571537 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066178 | CCTTTACTGTTGGCC[A/G]AAGGTGATCTCTTCG | 6045 |
rs775605187 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185046406 | TGCTAGTACCCACTT[A/T]TGCCGGGAGCCCACG | 6045 |
rs775610414 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102462 | TTTACAGTTTTAACC[A/G]TTTTAAGGCATGTAA | 6045 |
rs775713322 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057831 | AAAACAGTAAAACAG[-/T]TCAAAAATAATACAA | 6045 |
rs775719713 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086462 | TCAGTTCATTTATAT[C/T]GGGAAAGGAGGCAGA | 6045 |
rs775747915 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052567 | GATGGGGATGAAACT[A/G]CTTAATGGGTAAAGA | 6045 |
rs775765193 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185074192 | CTCCTGTCCTGTGGA[G/T]TTAGAGTGTATCACC | 6045 |
rs775797853 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094936 | CTCAGAAAACTTTCA[A/G]ATCTCATGGCTTTAG | 6045 |
rs775844225 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084769 | AAGAATGCATATAGC[A/C]GGAATTCTACCAGGA | 6045 |
rs775910102 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | RNF2 | GRCh38.p7 | 1:185087665 | AAGATGACTGCCAAG[A/G]GGCATATGAGACGTG | 6045 |
rs776058949 | snp | A/G | 1.64743e-05 | 0.00287 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185091647 | TGAATTAATGTGCCC[A/G]ATTTGTTTGGATATG | 6045 |
rs776062347 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185101586 | TATTTCCAACTTTAT[A/G]TATCACAGTATTTAA | 6045 |
rs776160530 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067799 | CTCGGCAACCTCTGC[C/T]TCCCGGGTTCAAACG | 6045 |
rs776160726 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082433 | TTGGCTCACTGCAAC[C/G]TCTGCCTCCCAGGTT | 6045 |
rs776251384 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185069042 | TTGCTGCCTTCTCCC[C/T]CATAACTACTCTGGT | 6045 |
rs776305305 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078614 | AAGGTGGCCTGGCGC[A/G]GTGGCTCACTCCTCC | 6045 |
rs776365162 | in-del | -/ATAT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185051810 | CACACCAATTTTTAC[-/ATAT]ATATACACACATTTT | 6045 |
rs776455269 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070525 | GATTATTTGAGAGCC[-/T]TGGGATCTCAAAGAG | 6045 |
rs776574130 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075447 | CTTTGCCAATGGTTC[A/G]ACAATTCCTGTTTCT | 6045 |
rs776624410 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064649 | TTTATTGGGATGTAA[C/T]CCCATGTAGGTCAAC | 6045 |
rs776634748 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185097798 | TCTTGGCCTCTCAAT[A/G]TGTTGGGTTTACAGG | 6045 |
rs776758031 | snp | A/C | 6.61802e-05 | 0.00575202 | missense | RNF2 | GRCh38.p7 | 1:185099960 | GCCAGTGGCCAGTTC[A/C]CTGTGAGTATTTAAA | 6045 |
rs776803596 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049000 | TGGGAGGCCGAAGTA[C/G]GTGGATCACGAGGTC | 6045 |
rs776848826 | snp | A/G | | | missense | RNF2 | GRCh38.p7 | 1:185100237 | TGGAATTGGTCAGTG[A/G]GAAATACTGGAAAGT | 6045 |
rs776868498 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087219 | ATTTATAAGCAATAG[-/A]AATGTATTACAGTTC | 6045 |
rs776888414 | snp | C/T | 3.34683e-05 | 0.0040906 | intron-variant | RNF2 | GRCh38.p7 | 1:185098051 | GTAAATTTTATGCAT[C/T]CTTTTTTCCCCCTTG | 6045 |
rs776951468 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069902 | TGGCAAATTTTGTTC[A/G]TTATAGAATAAGTCT | 6045 |
rs777024353 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099358 | CGGCCCAAATGAACA[-/T]TTCTATGGTTAGTCT | 6045 |
rs777034011 | in-del | -/AT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096264 | ATTGTGGTAAAAGAC[-/AT]ATAACAGAATTTTCC | 6045 |
rs777059298 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087631 | ATATGAGTTACAACG[A/G]ACACCTCAGGTAATG | 6045 |
rs777085027 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098757 | AATCCTCAAATTAAC[-/T]TTTTTTTTTTTTTGA | 6045 |
rs777141361 | in-del | -/AGCTC | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084248 | TTGGCTTTAATTGTT[-/AGCTC]AGCCTTAAACCATGC | 6045 |
rs777177224 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185071678 | CCAGTTCTTTGATAG[A/G]TTTCACCTGCTCATT | 6045 |
rs777179409 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047835 | ACAATTGGTTTTTAA[-/T]TCGTGTTATTGCACA | 6045 |
rs777188597 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047823 | ACGTACACATCTACA[A/G]TTGGTTTTTAATTCG | 6045 |
rs777265329 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072784 | TCTCTAATAAAAATA[C/T]AAAAAATCAGGCGGG | 6045 |
rs777280395 | snp | A/C | 1.70898e-05 | 0.00292311 | intron-variant | RNF2 | GRCh38.p7 | 1:185091538 | GCTTGTCCATAATAA[A/C]AAATTAAGTAGCTTT | 6045 |
rs777351221 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185096017 | AACATATTCTTTAAA[C/T]GCTGCCTGCAGTTAC | 6045 |
rs777370027 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059886 | GCCTTCAACTTTTCT[C/T]TCTCATCTTTCTGAA | 6045 |
rs777387164 | snp | G/T | 1.853e-05 | 0.00304379 | intron-variant | RNF2 | GRCh38.p7 | 1:185100154 | CATTTCATTATTATT[G/T]TGGTTTGTGCAGTTT | 6045 |
rs777401708 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087601 | ACCATTAAGCAAAAC[A/G]TGGGAACTCAGTTTA | 6045 |
rs777437576 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082056 | TCGTGGCAAGTTGCA[A/G]TCCAATGGTTCATTG | 6045 |
rs777532353 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045695 | GCGGAAGCAGCGGGC[C/T]GGGACACGCGTCTAC | 6045 |
rs777569023 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185069968 | GCTTATGAGGCACAT[C/T]AACCAAAGATTTTAG | 6045 |
rs777579701 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049262 | CAGAGGATGTGAGAA[C/T]TGGGACCACTGGGGA | 6045 |
rs777586963 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055042 | GATTGTATCTTGAGA[A/G]AACACCCCAAAAGTT | 6045 |
rs777655898 | in-del | -/AACT | 3.35374e-05 | 0.00409482 | intron-variant | RNF2 | GRCh38.p7 | 1:185100010 | GGGAGCACACTGACC[-/AACT]AACTGAGTGGCAAGT | 6045 |
rs777656215 | in-del | -/TGGTTAATTTCTCGAT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047879 | ATTGTCATCAGACAA[-/TGGTTAATTTCTCGAT]TGATTCATTTATTTG | 6045 |
rs777719061 | snp | C/T | | | intron-variant, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185046226 | GTTCCTCGGGGAGAC[C/T]CCTTCAGCTTCACAC | 6045 |
rs777791481 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094812 | CCTCTCTGACATTAT[C/T]GTCTGATTTATTCAG | 6045 |
rs777859801 | snp | C/G | 1.64768e-05 | 0.00287021 | synonymous-codon | RNF2 | GRCh38.p7 | 1:185098198 | TAGTAACAAACGGAC[C/G]AAAACATCTGATGAT | 6045 |
rs777869594 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057029 | GTTTTAAAACCTGGG[C/T]TGGGTGCGGTGGCTC | 6045 |
rs777929877 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091902 | CTCACTGCAACCTCT[G/T]CCTCCTGGGTTCAAG | 6045 |
rs777950361 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090705 | TCCTTTACAATTCTC[A/G]CCATACTAGAACTCT | 6045 |
rs777952611 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185072322 | TCCTCTTTTTATTTA[-/T]TCATCACCATTGATG | 6045 |
rs778027571 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077231 | GATTTTATAGTTAGC[C/T]ATCATTATTTGCACT | 6045 |
rs778064175 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065803 | TAAACTCTGGACACA[A/G]TGTCATCTACAAAGA | 6045 |
rs778066687 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099459 | CAGATTCTGGTCATT[A/G]GGGTTTGGGGGGTAT | 6045 |
rs778113393 | snp | A/G | 1.65737e-05 | 0.00287864 | missense | RNF2 | GRCh38.p7 | 1:185098332 | TGGAAAAAGATGACA[A/G]TGCACAGACGAGGTA | 6045 |
rs778203687 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053190 | TTTATTAAGGAAGGT[A/G]TTATTGTTATTATTC | 6045 |
rs778223466 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185066948 | TTTTAAAGGAAGCTT[C/T]AAAAATCTTAAAAAC | 6045 |
rs778276842 | in-del | -/CT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065677 | GAAACTCCTAGACAC[-/CT]CTGAAGGAACAAATT | 6045 |
rs778285927 | snp | G/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101947 | TGTTAAAGTTGTATA[G/T]ATTATTAATGCATGC | 6045 |
rs778428529 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185058347 | TTCAGAACCCCATGG[A/G]TACTCAGGGAGGACT | 6045 |
rs778455861 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086141 | CATCTCTACCAAAGC[C/T]TCCTTAACTCCTCAA | 6045 |
rs778626107 | snp | C/T | 1.8243e-05 | 0.00302013 | intron-variant | RNF2 | GRCh38.p7 | 1:185099741 | ATTTAAGTACATTTT[C/T]CTCATTGGCATATTC | 6045 |
rs778643197 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059672 | CTAAGAGCATGGCCT[C/T]CTCACTCAGACCTGG | 6045 |
rs778700689 | snp | C/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185043718 | GCACTCGTCATGAAG[C/G]AAGAAGGGAGATGCT | 6045 |
rs778702134 | snp | A/G | | | upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185045253 | CGAGGTGGCTGCGCC[A/G]TCATCCGGGCGTTGC | 6045 |
rs778705032 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073887 | CAGTTCAGTGGTTAC[A/G]CTACTCAGAGTGAGT | 6045 |
rs778882697 | snp | C/T | 1.65121e-05 | 0.00287329 | intron-variant | RNF2 | GRCh38.p7 | 1:185087685 | TATGAGACGTGTAAA[C/T]TGGGATACATTTTTA | 6045 |
rs778915119 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082858 | CAGCAAGTAACAAGT[A/C]GTTAGCAAAAAAACA | 6045 |
rs778946164 | in-del | -/TA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073845 | TCCAACTCTTTAGTC[-/TA]ACCAACTGGGTGTCC | 6045 |
rs779024268 | snp | C/T | | | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087582 | TGCAGACAAACGGAA[C/T]TCAACCATTAAGCAA | 6045 |
rs779025736 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095055 | CCACTGGCTTAAAGG[C/T]TAAAAGATGTGCTCC | 6045 |
rs779092216 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089545 | TTGGAATCATGGTGC[A/G]TTCTCATCATTGGTT | 6045 |
rs779110265 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075240 | CTCAGGTGATCCCCC[C/T]GCCTCGGCCTCCCAA | 6045 |
rs779139457 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090324 | GAGGAGAACATAGAT[A/G]GTTGAATTTATCCAG | 6045 |
rs779301218 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076540 | ATCCACCTGCCTTGG[C/T]CTCCCAAAGTGCTGG | 6045 |
rs779391214 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078051 | TGAGGTTCGAGACTA[A/G]CCCGGCCAACATGGG | 6045 |
rs779402239 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185080307 | TGTATTTCACATTCT[C/T]GGCTTGGGCAAGGGG | 6045 |
rs779437934 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | RNF2 | GRCh38.p7 | 1:185098133 | GAAGATAATGGTGAC[A/G]GTTCACACTGCAGTA | 6045 |
rs779454278 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083371 | TTTTAATTTTATTTT[A/G]TAAGTCCCGTATTTT | 6045 |
rs779473513 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185064152 | AATATTTCAATCTGT[C/T]TTAAATTTATATCAT | 6045 |
rs779477826 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084913 | ACCAGTCTGTTAACC[A/G]TTAGCTCCAGAGTAC | 6045 |
rs779477947 | in-del | -/A | | | intron-variant | RNF2 | GRCh38.p7 | 1:185086790 | GGTTTAAAGTGCTCT[-/A]AAAGTAGATTTTTTA | 6045 |
rs779617995 | in-del | -/ATAA | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056332 | AAAAAATTTTACAAG[-/ATAA]ATTATCCATCATTCT | 6045 |
rs779759522 | snp | C/T | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185101725 | TCAGTTTTGACAGAT[C/T]GGGGCCAGCTTGATG | 6045 |
rs779768280 | in-del | -/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054543 | ATTACGAGCGCTCTT[-/C]CTGAGAGCGGGTTCC | 6045 |
rs779797405 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067416 | TAACACCTGTATCCT[G/T]TAAGCAAGCATTGCT | 6045 |
rs779840455 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094063 | TCCCTACTTCTCTTC[A/C]TTCTTACTCATTTTG | 6045 |
rs779931512 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065789 | ACCACTGGAAGGCAT[A/G]AACTCTGGACACAAT | 6045 |
rs779935907 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092740 | GTGGGTATTTTTTCC[G/T]TGCAAAGCATGGATA | 6045 |
rs780027390 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185094091 | TTGGTTGATGGCAAT[C/T]CCATCATTCTACTTG | 6045 |
rs780045958 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185095538 | ACGTATCACTCTCTC[A/C]TGTGTTACCTGCTAC | 6045 |
rs780049914 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185087561 | TTCCAGCAATGTCTC[A/G]GGCTGTGCAGACAAA | 6045 |
rs780085627 | in-del | -/T | | | downstream-variant-500B | RNF2 | GRCh38.p7 | 1:185102797 | TCTGTTGATGGAGAC[-/T]TTTGGTATTGTGAAT | 6045 |
rs780089408 | in-del | -/TGTT | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071457 | GAAATTACAGCTATC[-/TGTT]TGGGAACAAAAGGAA | 6045 |
rs780104917 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | RNF2 | GRCh38.p7 | 1:185099906 | CAGATGAACCTTGAT[A/G]CAGCCAGTGAGAAGC | 6045 |
rs780197818 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049685 | TAAAAAAAAAAAAGC[A/G]GGGGAGGGGGGAACA | 6045 |
rs780229140 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067295 | TTTAGATTGAACTGC[A/G]GAAAGTGGTTTTTAT | 6045 |
rs780230825 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081505 | TTCAAGTGATTATCC[G/T]GCCTCAGCCTCCTGA | 6045 |
rs780282630 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185088111 | CAGAGATGCCAACTA[C/T]AGATGATTTTTATAT | 6045 |
rs780292156 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant | RNF2 | GRCh38.p7 | 1:185091785 | CTTAATTGTACCACG[A/G]AAGTGCTTTCCAGGG | 6045 |
rs780416857 | in-del | -/TGT | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077732 | TTTTTTTTTTTGGGC[-/TGT]TGTTGTTTGATTTCA | 6045 |
rs780431280 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185054691 | TCTTTGTGGGTTTTT[A/T]AAAATTTTTTATTAT | 6045 |
rs780435121 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185075930 | GAACGCATTGTTTTG[A/C]TTTGCAATTTACTGA | 6045 |
rs780526314 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185059091 | CTACTTCTGCCAGGA[G/T]TAAGCTTTTTTGTTG | 6045 |
rs780577741 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185056916 | TCAGTCTTATATTTT[A/G]CTCTATTTTCCTTTG | 6045 |
rs780711926 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085716 | TGGAGTGCAATGGCG[C/T]GATCTCAGCTCACTG | 6045 |
rs780806044 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185083329 | TTTAGCTACATGTTG[C/G]AGATTGTCCAAATTT | 6045 |
rs780882951 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098599 | TTCTCAGCAATGATA[C/G]TAGAGTACCAATAGG | 6045 |
rs780899304 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185084609 | ATTGCATATTTGGTA[C/G]TTTTTTTCCTTTCCT | 6045 |
rs781074012 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185057067 | TAATCCAGTACTTTG[A/G]GAGGCAGAAGCAGGA | 6045 |
rs781170772 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185071172 | TTTACATATGAAAAG[A/G]GGGAGTAGAGGAAAA | 6045 |
rs781209405 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185052670 | TGCCACTAAATGTTC[A/C]ATTTAAAATGGTTCA | 6045 |
rs781273101 | snp | A/G/T | 1.826e-05 | 0.00302153 | intron-variant | RNF2 | GRCh38.p7 | 1:185100172 | GTTTGTGCAGTTTTC[A/G/T]TAATTTTTTCTTTCT | 6045 |
rs781283968 | snp | G/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067069 | TTGGCAAATTACCTT[G/T]AAGTGCTTTCTGTTG | 6045 |
rs781296948 | in-del | -/G | 1.71634e-05 | 0.0029294 | intron-variant | RNF2 | GRCh38.p7 | 1:185099776 | AATGAAATTTTTAAT[-/G]ATTTATTCTTCTAGA | 6045 |
rs781305485 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185092495 | ATACATTTTCTGTAA[A/G]TGTTTGATTGAAAAC | 6045 |
rs781318216 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185076645 | AAAATTCACTTATTT[A/G]TTTAGGTATCTGATT | 6045 |
rs781363917 | snp | A/G | 1.65203e-05 | 0.002874 | missense, utr-variant-5-prime | RNF2 | GRCh38.p7 | 1:185091585 | CTTTTACAGGAGGCA[A/G]TAACAGATGGCTTAG | 6045 |
rs781379321 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185078396 | TCTTGTGAATGTTCC[C/T]CTTTATTTACTAGCC | 6045 |
rs781386220 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | RNF2 | GRCh38.p7 | 1:185098215 | AAACATCTGATGATT[C/T]TGGGCTAGAGCTTGA | 6045 |
rs781404684 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062716 | AATTAACACTCATGA[C/G]AGACAAAAGGTCAAT | 6045 |
rs781466673 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185093995 | TTTAGACATTTCTCC[A/T]TATGGGTATCTAATA | 6045 |
rs781471385 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185065992 | GCATCTACACAGCCA[C/G]AAGCTTAGGAGTCCT | 6045 |
rs781552080 | snp | A/C | | | intron-variant | RNF2 | GRCh38.p7 | 1:185089184 | GGGTTCGGACTCTTA[A/C]GAGAGTCTAATGCCA | 6045 |
rs781613105 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185073493 | TTCCAGTCTGTTCTT[C/T]TAGTGTATTCTCTTT | 6045 |
rs781717529 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185087869 | GTGAATAAAACAGAT[A/G]TAGCACCAACCATGG | 6045 |
rs796067286 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185049695 | AAAGCGGGGGAGGGG[A/G]GAACATTACAGTAAT | 6045 |
rs796185363 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185067722 | CCTTTTTTTTTTTTT[C/T]TTTTTTGAGACGGAG | 6045 |
rs796225336 | in-del | -/TTG | | | intron-variant | RNF2 | GRCh38.p7 | 1:185055417 | TAGGTTTTTGTTTGT[-/TTG]TTGTTGTTGTTTTTA | 6045 |
rs796245766 | snp | A/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185068698 | CTGTGAGAGAATAAC[A/T]TACTGTTGTTATAAG | 6045 |
rs796280734 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185048070 | TTCTACCCTTTCTAC[C/G]TAATGTGTCTACTGG | 6045 |
rs796310068 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053340 | CTTTTTTTCTTTTTC[-/T]TTTTTTTTTTTAAGA | 6045 |
rs796472816 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185053327 | TTTGCTTCATTTTCC[-/T]TTTTTTCTTTTTCTT | 6045 |
rs796508345 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185085148 | TTCTTTCTTTTTCTT[C/T]TTTTTTTTTTTTTTT | 6045 |
rs796513130 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185081592 | AGAGACGGGTGGGGT[C/G]GGGGGGGGCGGTTTC | 6045 |
rs796611547 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185062290 | CATTTATTGTTGACA[A/G]TGTAGGAAGTTATAG | 6045 |
rs796656786 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185061472 | AACCCCGAATGTGCA[A/G]CCTTTAGCACCAAGG | 6045 |
rs796674692 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185090209 | ACAGGTGTGAGCCAT[C/T]GTGCCTGGCCGAGGC | 6045 |
rs796679310 | in-del | -/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185082534 | TTTTTATTTTTTTTT[-/T]AGTAGAGACAGGGTT | 6045 |
rs796706190 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098961 | TTCACCATGTTGGCC[A/G]GGATGGTCTCGATCT | 6045 |
rs796741459 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185091009 | TATAAAATTGCTCTG[C/T]GGAAAAGAATTTTCG | 6045 |
rs796756256 | in-del | -/TC | | | intron-variant, upstream-variant-2KB | RNF2 | GRCh38.p7 | 1:185070641 | TATTTTCTTTTCTTT[-/TC]TTTTTTTTTTTTTTT | 6045 |
rs796776375 | snp | C/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185099397 | ATTTTAATTCTTAGA[C/G]AATAAGAAATTTGCT | 6045 |
rs796855267 | snp | A/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185047250 | GCCCGAGTCAGGCCA[A/G]TCCGTTTGAGTATTT | 6045 |
rs796895484 | in-del | -/G | | | intron-variant | RNF2 | GRCh38.p7 | 1:185077624 | TTAGGAATTAACTTT[-/G]GTTTTTTTTTTTTTG | 6045 |
rs796980578 | snp | C/T | | | intron-variant | RNF2 | GRCh38.p7 | 1:185098837 | GCTCACTGCAGCCTC[C/T]GCCTCCTGGGTTCAA | 6045 |
rs797012643 | snp | A/G | | | utr-variant-3-prime | RNF2 | GRCh38.p7 | 1:185100806 | CTGTCCTTAAAAACA[A/G]TTCTCATAGGATTAT | 6045 |