SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1954612 | snp | A/G | 0.0230396 | 0.104828 | intron-variant | RNF128 | GRCh38.p7 | X:106752747 | cccagagtaacagag[A/G]tatgtgaccttttag | 79589 |
rs1991340 | snp | C/T | 0.31164 | 0.242282 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693176 | AATTTTTGTGCCCCA[C/T]GTGTTATACTCTAAA | 79589 |
rs2880013 | snp | A/C | 0.383653 | 0.211275 | intron-variant | RNF128 | GRCh38.p7 | X:106773321 | AATATAGAAAATAAA[A/C]CTTTGAGAAGAGCTG | 79589 |
rs3037086 | snp | C/G | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693399 | TCTCTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT | 79589 |
rs3037090 | in-del | -/GT | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693361 | tgtgtgtgtgtgtgt[-/GT]tTTCTTAGCAGGCTC | 79589 |
rs3210994 | snp | G/T | | | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106796945 | AATATGTCCCAATTT[G/T]TATTGATTCTCttta | 79589 |
rs3221753 | microsatellite | (CA)20/21/22/23/24 | 0.694702 | 0.143393 | intron-variant | RNF128 | GRCh38.p7 | X:106779350 | CTTAAGTATCCTCAA[(CA)20/21/22/23/24]GTAACTGTGTAGGGA | 79589 |
rs3764774 | snp | C/T | 0.0297427 | 0.118265 | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106796632 | AATGGGCTAAAATTA[C/T]ATTAGATAAACTAAA | 79589 |
rs3916760 | snp | C/G | 0.109764 | 0.206963 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693401 | tctctctctctctct[C/G]tgtgtgtgtgtgtgt | 79589 |
rs4614136 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106764884 | GAGAGATGGCTCTTA[A/G]AGAAAAGACAAATAA | 79589 |
rs4826943 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | RNF128 | GRCh38.p7 | X:106764661 | aaggagcgaaactcc[A/G]tctcaaaaaaaacaa | 79589 |
rs5020422 | snp | A/G | 0.266995 | 0.249422 | intron-variant | RNF128 | GRCh38.p7 | X:106764653 | CTCTGGGTAAGGAGC[A/G]AAACTCCGTCTCAAA | 79589 |
rs5903288 | in-del | -/GAGAGA | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693426 | AGAGAGAGAGAGAGA[-/GAGAGA]AATTAGAAGAGAAAA | 79589 |
rs5903289 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106712046 | AGTTTTGCCATTAAT[-/A]TTAATTACCTGCATG | 79589 |
rs5916766 | snp | C/T | 0.0204488 | 0.0990265 | intron-variant | RNF128 | GRCh38.p7 | X:106721353 | GTGAGAAGCCAGATA[C/T]AGTGTCTCATTCCTT | 79589 |
rs5916767 | snp | C/G | 0.025682 | 0.110762 | intron-variant | RNF128 | GRCh38.p7 | X:106746901 | GCTTGAGAATTTCTC[C/G]TAGAATTGGAATCTG | 79589 |
rs5917017 | snp | A/G | 0.0220041 | 0.102557 | intron-variant | RNF128 | GRCh38.p7 | X:106735434 | CCTGCAACTAAAAGC[A/G]TCTTAGCTTTTAAAA | 79589 |
rs5917020 | snp | A/C | 0.212407 | 0.247157 | intron-variant | RNF128 | GRCh38.p7 | X:106786592 | agtccaaaaaagaaa[A/C]aagttgatacatttg | 79589 |
rs5917021 | snp | G/T | 0.0068637 | 0.0581785 | intron-variant | RNF128 | GRCh38.p7 | X:106794806 | attccaatcccacac[G/T]acagggttcattcta | 79589 |
rs5962356 | snp | A/C | 0.225906 | 0.248836 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692331 | GGCTAGTAGCAAAAT[A/C]ATGAACTATTTGTGT | 79589 |
rs5962357 | snp | A/G | 0.306072 | 0.243631 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693447 | GAAGAGAAAAAAGCA[A/G]TAAAATTCATTCTAC | 79589 |
rs5962358 | snp | C/T | 0.225513 | 0.248798 | intron-variant | RNF128 | GRCh38.p7 | X:106696199 | gatagttaacattta[C/T]tggcatttactatat | 79589 |
rs5962359 | snp | A/C | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106706158 | CCCTGGGTTGCTATT[A/C]ATTCTTGTTTACTTG | 79589 |
rs5962360 | snp | A/G | 0.306072 | 0.243631 | intron-variant | RNF128 | GRCh38.p7 | X:106714444 | AAGAAATAGATCTGT[A/G]TACCCTTCATCCCTT | 79589 |
rs5962361 | snp | C/T | 0.306072 | 0.243631 | intron-variant | RNF128 | GRCh38.p7 | X:106714872 | atccagattgttgca[C/T]atattaatagctcct | 79589 |
rs5962362 | snp | A/T | 0.266995 | 0.249422 | intron-variant | RNF128 | GRCh38.p7 | X:106739688 | AAAAGATAAGGACAT[A/T]AGTGAGACAGATTCA | 79589 |
rs5962363 | snp | A/C | 0.0430067 | 0.140192 | intron-variant | RNF128 | GRCh38.p7 | X:106791463 | TTATTTACAAAAGAA[A/C]GATTTATTGGAAAGC | 79589 |
rs5962364 | snp | C/T | 0.118606 | 0.212687 | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106796816 | GTGTGGCTTTTGTTT[C/T]AGAATTTTGTTCAAA | 79589 |
rs5962722 | snp | A/G | 0.221574 | 0.248379 | intron-variant | RNF128 | GRCh38.p7 | X:106699400 | CTTGCTGCCTCCTCT[A/G]CCTGAGTCACTTCTC | 79589 |
rs5962723 | snp | C/T | 0.23137 | 0.249305 | intron-variant | RNF128 | GRCh38.p7 | X:106699494 | tctagtacaggctac[C/T]gccagctctcgcact | 79589 |
rs5962724 | snp | A/T | 0.221574 | 0.248379 | intron-variant | RNF128 | GRCh38.p7 | X:106699759 | ttccctctccctcac[A/T]atgcttcaaccactc | 79589 |
rs5962725 | snp | A/T | 0.22669 | 0.248911 | intron-variant | RNF128 | GRCh38.p7 | X:106702162 | ATGTTTATAAGGAAA[A/T]CAAGATATAGTACCT | 79589 |
rs5962726 | snp | A/G | 0.0787474 | 0.182133 | intron-variant | RNF128 | GRCh38.p7 | X:106705045 | GGGTTTGTTCCTAGA[A/G]CTATGATTGTAGATC | 79589 |
rs5962727 | snp | G/T | 0.226298 | 0.248874 | intron-variant | RNF128 | GRCh38.p7 | X:106705162 | CTAACCCGCCCTAGG[G/T]TTCCAAATGGAACTG | 79589 |
rs5962728 | snp | C/T | 0.226298 | 0.248874 | intron-variant | RNF128 | GRCh38.p7 | X:106707384 | ttttccttgttgtgc[C/T]ttcctgagcaatata | 79589 |
rs5962729 | snp | A/T | 0.220783 | 0.248287 | intron-variant | RNF128 | GRCh38.p7 | X:106710824 | AATAGCCAACTATAT[A/T]CTGGCCAATTTAATT | 79589 |
rs5962730 | snp | C/T | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106710950 | TATGTGGACAACATA[C/T]GCAGCTGAACTGTGC | 79589 |
rs5962731 | snp | G/T | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106712142 | AGTCACGTCTTTATA[G/T]GTCTGAAGAGAATGC | 79589 |
rs5962732 | snp | C/T | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106712195 | ATGTGCTGAAAAATG[C/T]ATTTCAAAGCCAACT | 79589 |
rs5962734 | snp | A/G | 0.220783 | 0.248287 | intron-variant | RNF128 | GRCh38.p7 | X:106715039 | gctttctgtgaatgt[A/G]atttttcatttttct | 79589 |
rs5962735 | snp | A/T | 0.21999 | 0.248192 | intron-variant | RNF128 | GRCh38.p7 | X:106719200 | CCCATTGCCTGTAGA[A/T]TAAAAAAAAAAATTA | 79589 |
rs5962736 | snp | C/T | 0.318726 | 0.240368 | intron-variant | RNF128 | GRCh38.p7 | X:106738280 | aatacctacATTTTC[C/T]ATGATATTATAAATC | 79589 |
rs5962737 | snp | A/G | 0.318088 | 0.24055 | intron-variant | RNF128 | GRCh38.p7 | X:106748214 | TGTACAGGAATCTAT[A/G]TATTAGCATATCAAC | 79589 |
rs5962738 | snp | A/G | 0.119531 | 0.213255 | intron-variant | RNF128 | GRCh38.p7 | X:106751981 | ctgcttgaggaaagg[A/G]gagtgaaaagtaaaa | 79589 |
rs5962739 | snp | C/T | 0.266995 | 0.249422 | intron-variant | RNF128 | GRCh38.p7 | X:106753700 | caactagctgccatc[C/T]ttaagaaacacactt | 79589 |
rs5962740 | snp | A/G/T | 0.266995 | 0.249422 | intron-variant | RNF128 | GRCh38.p7 | X:106753701 | aactagctgccatcc[A/G/T]taagaaacacacttc | 79589 |
rs5962741 | snp | C/T | 0.26988 | 0.249208 | intron-variant | RNF128 | GRCh38.p7 | X:106762401 | gctcaccacaacctc[C/T]gcctcgggttcaagc | 79589 |
rs5962742 | snp | A/C | 0.221179 | 0.248333 | intron-variant | RNF128 | GRCh38.p7 | X:106765812 | atgttggtgtgctgc[A/C]cccattaactaactc | 79589 |
rs5962743 | snp | A/G | 0.3152 | 0.241348 | intron-variant | RNF128 | GRCh38.p7 | X:106768119 | ggattcggcttgcca[A/G]tatcttattgaggat | 79589 |
rs5962745 | snp | A/T | 0.11768 | 0.212112 | intron-variant | RNF128 | GRCh38.p7 | X:106769278 | tatccttgttaactt[A/T]ctgtctcgttgatct | 79589 |
rs5962746 | snp | C/T | 0.315522 | 0.241261 | intron-variant | RNF128 | GRCh38.p7 | X:106769705 | agtctgtgtcttttt[C/T]ttttcagtctatgtc | 79589 |
rs5962747 | snp | C/T | 0.235625 | 0.249586 | intron-variant | RNF128 | GRCh38.p7 | X:106771557 | accctctgagccagg[C/T]gcgggttataatctc | 79589 |
rs5962748 | snp | A/G | 0.267718 | 0.249371 | intron-variant | RNF128 | GRCh38.p7 | X:106773474 | TTACAAAAACATTTC[A/G]TACTCAATATAGAAA | 79589 |
rs5962749 | snp | C/T | 0.268079 | 0.249345 | intron-variant | RNF128 | GRCh38.p7 | X:106777184 | CAAATATATTTGAGA[C/T]ATTGAACTAAAAACT | 79589 |
rs5962751 | snp | A/G | 0.268079 | 0.249345 | intron-variant | RNF128 | GRCh38.p7 | X:106790551 | GGCATCCCTCTTTCT[A/G]TTTTTGTAATCTTTT | 79589 |
rs5962752 | snp | C/T | 0.118606 | 0.212687 | intron-variant | RNF128 | GRCh38.p7 | X:106793569 | caactggcccactaa[C/T]gtcctttttctgtcc | 79589 |
rs6523884 | snp | A/C | 0.306072 | 0.243631 | intron-variant | RNF128 | GRCh38.p7 | X:106713549 | CTGAATGTTCTAGAG[A/C]aatgctgtccaacag | 79589 |
rs6523886 | snp | C/T | 0.252304 | 0.249989 | intron-variant | RNF128 | GRCh38.p7 | X:106722855 | ATAAGTAGGGTTGCT[C/T]GGTGAGGATGAACTC | 79589 |
rs6523887 | snp | C/T | 0.246679 | 0.249978 | intron-variant | RNF128 | GRCh38.p7 | X:106723310 | gcggtggctcacgcc[C/T]gtaatcccagcactt | 79589 |
rs6523888 | snp | C/T | 0.247056 | 0.249983 | intron-variant | RNF128 | GRCh38.p7 | X:106727451 | GCCATGGCCAGTTTC[C/T]CTTATTTTCCTCATT | 79589 |
rs6523889 | snp | A/G | 0.247056 | 0.249983 | intron-variant | RNF128 | GRCh38.p7 | X:106730668 | ATACTTGCTTGTACA[A/G]TTTTCCTTGAGTCAA | 79589 |
rs6616612 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | RNF128 | GRCh38.p7 | X:106737799 | ATTCCAAAATACTTT[C/T]ATAGGTGTGTTTCAA | 79589 |
rs6616613 | snp | C/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106765636 | TACAACAGAGGGTGT[C/G]TACATTTCAGACATT | 79589 |
rs6622105 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106706834 | tgcacaatgtctatt[C/G]tatagtagacAGTAA | 79589 |
rs6622111 | snp | A/T | 0.324109 | 0.238763 | intron-variant | RNF128 | GRCh38.p7 | X:106772108 | CATGAGCAATCTGAC[A/T]TTCTTTTAACATTGG | 79589 |
rs7050108 | snp | A/G | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106715621 | ACCTTGACTGTAGAC[A/G]GAATTGAGAGAATAC | 79589 |
rs7050209 | snp | C/T | 0.305742 | 0.243707 | intron-variant | RNF128 | GRCh38.p7 | X:106715579 | ACTAGGAAAATAGGA[C/T]CCAGGAACAAAACTT | 79589 |
rs7052171 | snp | C/T | 0.318088 | 0.24055 | intron-variant | RNF128 | GRCh38.p7 | X:106743803 | aaagacacatgcaca[C/T]gtatgtttattgcag | 79589 |
rs7053530 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106747944 | actctctatagcccc[A/T]caggctagcatagtg | 79589 |
rs7061079 | snp | C/T | 0.102711 | 0.202005 | intron-variant | RNF128 | GRCh38.p7 | X:106696338 | CTGCCAAATAGTGTG[C/T]CATTGGATTTTTTCC | 79589 |
rs7062754 | snp | A/G | 0.172111 | 0.237557 | intron-variant | RNF128 | GRCh38.p7 | X:106772164 | TTTTCCACAAAACTT[A/G]TATAATTGGTGGTAG | 79589 |
rs7063642 | snp | A/G | 0.266995 | 0.249422 | intron-variant | RNF128 | GRCh38.p7 | X:106772750 | ATGCGTGTTTATATA[A/G]CCTACAACTTTCATA | 79589 |
rs7065970 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106737430 | tataaaatggcatag[A/T]atttgtatataatat | 79589 |
rs7471058 | snp | A/G | 0.26916 | 0.249265 | intron-variant | RNF128 | GRCh38.p7 | X:106764646 | cactccactctgggt[A/G]aggagcgaaactccg | 79589 |
rs7877910 | snp | A/G | 0.0394543 | 0.134798 | intron-variant | RNF128 | GRCh38.p7 | X:106782487 | AAAACATCAAAAGAC[A/G]GATGAGTTATGGATG | 79589 |
rs7884740 | snp | A/C | 0.0121112 | 0.0768695 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692451 | GATGCTAGTAGTACC[A/C]GGTACTATGGGAGGG | 79589 |
rs7885282 | snp | A/T | 0.0379276 | 0.132383 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692036 | ATGGATTTAGGTAAC[A/T]TCTCATTAATCTGCT | 79589 |
rs7890657 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106728281 | CACGTGTAATAGcag[C/T]gtatcatagttttta | 79589 |
rs10521511 | snp | A/G | 0.0714214 | 0.174956 | intron-variant | RNF128 | GRCh38.p7 | X:106750335 | TAGGTTTCATTGAAG[A/G]TAACTAGTGTAGAAT | 79589 |
rs11326354 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106710771 | AAAAAAAAAAAAAAA[-/A]GCTGATCTGGGTGCC | 79589 |
rs11328315 | in-del | -/T | 0.0348667 | 0.127349 | intron-variant | RNF128 | GRCh38.p7 | X:106719229 | TACTGCCCATGGGCA[-/T]TTTTTTTTTTTTGAA | 79589 |
rs11443623 | in-del | -/A | 0.224335 | 0.248679 | intron-variant | RNF128 | GRCh38.p7 | X:106713369 | AAAAATTAGTAGGGC[-/A]TGGTGGCGCAGCCTG | 79589 |
rs11556755 | snp | A/G | | | intron-variant, utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106726894 | CCAGGGGCGCTAGGG[A/G]ACTGCGGAGCGCGCG | 79589 |
rs12007076 | snp | A/G | 0.0256233 | 0.11025 | intron-variant | RNF128 | GRCh38.p7 | X:106775512 | AAATGGTCAAGAATA[A/G]CATTAAAACTTCTCA | 79589 |
rs12009098 | snp | C/T | 0.223547 | 0.248597 | intron-variant | RNF128 | GRCh38.p7 | X:106716708 | AGTGATGTGCCAGAG[C/T]AAGATCTGTGGCTAC | 79589 |
rs12009433 | snp | A/C | 0.225513 | 0.248798 | intron-variant | RNF128 | GRCh38.p7 | X:106717508 | ATCTTTTCTTGATAC[A/C]GTTAATAGGGTTAAC | 79589 |
rs12010347 | snp | A/T | 0.0787474 | 0.182133 | intron-variant | RNF128 | GRCh38.p7 | X:106715709 | ATTTTCTAGCAAGTA[A/T]CTGTAGTGCAGATAT | 79589 |
rs12014636 | snp | C/T | 0.306072 | 0.243631 | intron-variant | RNF128 | GRCh38.p7 | X:106716602 | atgtaaattatacct[C/T]aacaaaaaCGTTAGG | 79589 |
rs12392745 | snp | C/T | 0.268079 | 0.249345 | intron-variant | RNF128 | GRCh38.p7 | X:106783857 | gagagagggagcagg[C/T]gccaggctcttttaa | 79589 |
rs12556197 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789415 | atataatatatatac[A/T]ctacataatatatag | 79589 |
rs12556200 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789428 | actctacataatata[G/T]agtatatattatata | 79589 |
rs12558156 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789429 | ctctacataatatat[A/T]gtatatattatatac | 79589 |
rs12558173 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789419 | aatatatatactcta[C/T]ataatatatagtata | 79589 |
rs12558279 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106754058 | ccggacagaaaatcc[A/C]caaagaaatatcaca | 79589 |
rs12837722 | snp | A/G | 0.217606 | 0.247892 | intron-variant | RNF128 | GRCh38.p7 | X:106747433 | TTAGAAAAATAGGAT[A/G]AAATTAATAAATGAT | 79589 |
rs12838370 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106754414 | gttttctttctcttt[A/T]ttttttttttttttt | 79589 |
rs12841228 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | RNF128 | GRCh38.p7 | X:106751630 | gctcacagctctggg[A/G]ggagaggaaagatta | 79589 |
rs12843493 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106747834 | AGATATATACAATTC[A/T]TTTCACTGGCTTGGA | 79589 |
rs12843965 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106747988 | tagatattcagtaaa[A/C]cacttaatgaatgaa | 79589 |
rs12844347 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106747906 | ATTTGCAAGTGTGTA[A/G]AGGGCAGGGACTGCA | 79589 |
rs12845540 | snp | G/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106747865 | TCATATTCTTCCTAG[G/T]GATGAATATCTAACA | 79589 |
rs12851524 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106786239 | ttatagatcaaagaa[A/G]cagaagagagagtac | 79589 |
rs12851744 | snp | C/T | 0 | 0 | missense | RNF128 | GRCh38.p7 | X:106694360 | GATGCTGTTGTGATT[C/T]ACAATGCTCCAGAGA | 79589 |
rs12851881 | snp | A/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106742224 | GTACATTACATACTG[A/T]GGAAAACAAAATAAT | 79589 |
rs12852310 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106779317 | tgtaaaatgattgac[A/T]taaattaatacatct | 79589 |
rs12852323 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106779329 | gacataaattaatac[A/C]tctatccctacacag | 79589 |
rs12853210 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106773729 | TTCTACCATATTATA[A/C]CAGTGTATAAAAAGG | 79589 |
rs12853410 | snp | G/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106786225 | gaaaaaggatagatt[G/T]atagatcaaagaaac | 79589 |
rs12853411 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106786227 | aaaaggatagattta[G/T]agatcaaagaaacag | 79589 |
rs12854435 | snp | A/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106742335 | CTTTGACCTTAATGT[A/T]TGAAAAGCTATAAAC | 79589 |
rs12854686 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106779262 | taaaatttgtatata[A/T]tcaaggtgtacaaca | 79589 |
rs12854784 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106779330 | acataaattaataca[C/T]ctatccctacacagt | 79589 |
rs12857597 | snp | A/C | 0.219197 | 0.248095 | intron-variant | RNF128 | GRCh38.p7 | X:106739105 | TTTCTCTCTTCTATT[A/C]TCTTCTCTTCTcttc | 79589 |
rs12857865 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106746498 | TACAAATAAGATTAG[A/C]CAAAAACCATAATAT | 79589 |
rs12857939 | snp | G/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106783172 | TCCTGTGACAGCAAA[G/T]AAATACTTTGGCTAA | 79589 |
rs12860012 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106718122 | AACCAATAGAAGGCC[C/T]TAAAACCAGGAGGGA | 79589 |
rs16986268 | snp | A/T | 0.250061 | 0.25 | intron-variant | RNF128 | GRCh38.p7 | X:106721750 | CTCTCCAGAGGGAAA[A/T]TAGTTAAGTCATTAT | 79589 |
rs16986538 | snp | A/G | 0.100346 | 0.200259 | intron-variant | RNF128 | GRCh38.p7 | X:106779897 | TACCTAAACAGCTAC[A/G]TGGCTCAGACTTTTA | 79589 |
rs16986564 | snp | A/G | 0.171252 | 0.237274 | intron-variant | RNF128 | GRCh38.p7 | X:106781529 | CTTGGAACTCTTGCT[A/G]TCAGTGTCACAGTGA | 79589 |
rs17279512 | snp | A/C | 0.0312828 | 0.12109 | intron-variant | RNF128 | GRCh38.p7 | X:106696483 | ATTATTTTATGCCAA[A/C]ATTTTGTTTGTTGTT | 79589 |
rs28587204 | snp | C/T | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692063 | TGCTTTTAAAGTTTT[C/T]CATGAGAAGATTTTT | 79589 |
rs28631805 | snp | C/T | 0.0409784 | 0.137149 | intron-variant | RNF128 | GRCh38.p7 | X:106697893 | GGGTTATATTCTGCA[C/T]TGGTGAGTATATCTC | 79589 |
rs28669895 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106784423 | TGCTTTTGCATATCC[A/C]GACACATCTAGATAT | 79589 |
rs28674635 | snp | A/G | 0.230982 | 0.249276 | intron-variant | RNF128 | GRCh38.p7 | X:106700311 | TTATAGTCGTGAGCC[A/G]TCGCACTTGGCCTAA | 79589 |
rs34125087 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106793681 | TTGACACTTCTGAAG[-/T]ATTACTGGTCAGTTA | 79589 |
rs34222080 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106793402 | TTCAGACTGACTGAC[-/A]AAAAACGTTTCAAAA | 79589 |
rs34354678 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106722085 | AAAGGTCCTGGTGGA[-/G]GTAGTGATATGGCCA | 79589 |
rs34358229 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106791883 | AATTATTTTCCCTTT[-/G]CTTTTACCTCAATCT | 79589 |
rs34595270 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106780283 | CTTTGCTTTCACCAT[-/G]AATTTCAAAATTGAA | 79589 |
rs34619446 | snp | A/T | 0.0204488 | 0.0990265 | intron-variant | RNF128 | GRCh38.p7 | X:106737082 | CATGTACTTCACCTT[A/T]AAGACTACATTTTGT | 79589 |
rs34668682 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106738458 | AGAAGCAGAAAAAAC[-/G]GGAACATCCATATTG | 79589 |
rs34894832 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106760512 | AGGATGTGGAGAAAA[-/G]GGGAACTCTTATATA | 79589 |
rs34939748 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106772322 | CTGTGTAAAACCTTA[-/G]GAACACCTTGAGCAA | 79589 |
rs35007941 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106774211 | TCCTCCAACTTTACT[-/G]CTCAATTTGTATTTT | 79589 |
rs35091426 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106737846 | CCAGTTCATTTTGGC[-/A]AAAGGGCAGGATATG | 79589 |
rs35188999 | in-del | -/G | | | intron-variant, frameshift-variant | RNF128 | GRCh38.p7 | X:106727336 | GAGAGAGGGGCGTCT[-/G]GGAGCCGTCATCTTT | 79589 |
rs35256073 | in-del | -/G | | | frameshift-variant | RNF128 | GRCh38.p7 | X:106791190 | ATATGCTTCAGTACA[-/G]GGGAACAGATGAACC | 79589 |
rs35450372 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106765211 | AAAATAGTGTCTTTT[-/G]GGAATGTTAAGGATC | 79589 |
rs35496501 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106761294 | CAGATGTTAACAAGG[-/T]TTTAGAGAAAAGGGA | 79589 |
rs35567509 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106780669 | CTGGCTTTAAAGGGG[-/T]TTTTTAAATTTCCTT | 79589 |
rs35647372 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106707685 | GTCCCCCTCCCCAAC[-/A]AATATTCTCCTCCCT | 79589 |
rs35675771 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106760412 | AATCATCAGGAAAAT[-/G]GCAAATCAAAACTGC | 79589 |
rs35680614 | in-del | -/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106730110 | CTGAGTGTCTATATT[-/C]CCCACCTAACTAATT | 79589 |
rs35790560 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106694523 | TAATTTTACTTTAAA[-/T]TTTTCTTGCCTGGCA | 79589 |
rs35797977 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106730067 | AGGGGCCTGCACTTG[-/A]AATTGTTTGCCCTTG | 79589 |
rs35936030 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106784518 | TTATAAGCACCAATA[-/T]TTTTTCTTAATACCA | 79589 |
rs36032530 | in-del | -/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106736887 | ATGTTGTCTCTACTT[-/C]CCAAAGAACTGGTTT | 79589 |
rs36056417 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106789221 | AATACATATATATAA[-/G]ATTCCAACTAAGGAG | 79589 |
rs55658305 | in-del | -/TTAA | | | intron-variant | RNF128 | GRCh38.p7 | X:106738818 | ATTGTGAGGTGTAAA[-/TTAA]ATAATATATGTACAG | 79589 |
rs55845652 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | RNF128 | GRCh38.p7 | X:106746865 | CTCTAGCCATGTCTC[A/G]TTATTATTAATGACT | 79589 |
rs55870405 | in-del | -/A/AA | | | intron-variant | RNF128 | GRCh38.p7 | X:106704454 | AAAAAAAAAAAAAAA[-/A/AA]GAGCTGGGGAGTAGT | 79589 |
rs56121637 | snp | A/T | 0.011491 | 0.074923 | missense | RNF128 | GRCh38.p7 | X:106773038 | CATGGCCCTTGGGTG[A/T]ATCACTATTCAATTT | 79589 |
rs56229155 | in-del | -/TTT | | | intron-variant | RNF128 | GRCh38.p7 | X:106719239 | GGGCATTTTTTTTTT[-/TTT]GAAACAGAGTCTCTG | 79589 |
rs56711259 | snp | A/C/T | 0.246679 | 0.249978 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725110 | AATGCTCTTCACCAG[A/C/T]AAAATCAGACAATTT | 79589 |
rs57488487 | snp | A/G | 0.116289 | 0.211238 | intron-variant | RNF128 | GRCh38.p7 | X:106765719 | TTTTATATTTTGTTG[A/G]TTTTTTTATTATTAT | 79589 |
rs57800754 | snp | C/T | 0.0437711 | 0.141314 | intron-variant | RNF128 | GRCh38.p7 | X:106785182 | TTTAAAGCAGTGCTA[C/T]CAAGCCATTGTTCAG | 79589 |
rs58157584 | in-del | -/GT/GTGG/GTTT | | | intron-variant | RNF128 | GRCh38.p7 | X:106779390 | TGTGTGTGTGTGTGT[-/GT/GTGG/GTTT]TGAGGATACTTAAGA | 79589 |
rs58225155 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106780032 | ATTTTTAAAATATGG[A/T]GACTTAAGTACAGAA | 79589 |
rs58228930 | snp | A/G | 0.0404706 | 0.136372 | intron-variant | RNF128 | GRCh38.p7 | X:106703342 | TGTTAACTATGTGCC[A/G]AGCATTCTTCTCAGT | 79589 |
rs58451729 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106788396 | TATATATAATATATA[A/T]TATATATAATATATA | 79589 |
rs58561066 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789406 | ATGTACATTATATAA[-/T]ATATATACTCTACAT | 79589 |
rs58640891 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106789409 | TACATTATATAATAT[-/A]TATACTCTACATAAT | 79589 |
rs58662057 | snp | A/G | 0.171682 | 0.237416 | intron-variant | RNF128 | GRCh38.p7 | X:106740109 | TGCCCCTTTATGACC[A/G]GCATTATGCTGAATG | 79589 |
rs59124700 | in-del | -/A | 0.118143 | 0.2124 | intron-variant | RNF128 | GRCh38.p7 | X:106780370 | CCATTCAGAATCAAG[-/A]AAAAAAAACCATGTA | 79589 |
rs59213928 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106789405 | TATGTACATTATATA[A/C]TATATATACTCTACA | 79589 |
rs59232810 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106708972 | AGCACTAGAAAAATT[-/T]GTGGGGTCTTTTTTT | 79589 |
rs59737530 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106788357 | AATATATATTATATA[C/T]TATATATAATATATA | 79589 |
rs59889624 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106714193 | AAAAAAAAAAAAAAA[-/A]GAACTACCATAGCAG | 79589 |
rs60118152 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106789396 | ATGTATATATATGTA[C/T]ATTATATAATATATA | 79589 |
rs60596381 | snp | A/C | 0.101293 | 0.200963 | intron-variant | RNF128 | GRCh38.p7 | X:106699518 | TCGCACTGACTACTG[A/C]AAATAGCCTCCAAAC | 79589 |
rs60744409 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106788412 | TATATATAATATATA[A/T]TATATAATATATATT | 79589 |
rs60813323 | in-del | -/AA | | | intron-variant | RNF128 | GRCh38.p7 | X:106710770 | AAAAAAAAAAAAAAA[-/AA]GCTGATCTGGGTGCC | 79589 |
rs60855137 | in-del | -/A | 0.265183 | 0.249539 | intron-variant | RNF128 | GRCh38.p7 | X:106761600 | ATATTATACAGCCAT[-/A]AAAAAAGAATGAGAT | 79589 |
rs61251410 | snp | A/G | 0.246679 | 0.249978 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725276 | CCTTTTCAATACCTA[A/G]GAGTATATGTTTCAC | 79589 |
rs61286394 | in-del | -/TTATATATA | | | intron-variant | RNF128 | GRCh38.p7 | X:106788396 | TATATATAATATATA[-/TTATATATA]ATATATAATATATAA | 79589 |
rs61392472 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106789393 | TTTATGTATATATAT[A/G]TACATTATATAATAT | 79589 |
rs61425782 | in-del | -/TATATAT | | | intron-variant | RNF128 | GRCh38.p7 | X:106788381 | ATATATATTATATAT[-/TATATAT]AATATATATTATATA | 79589 |
rs61744860 | snp | A/G | 0.0512465 | 0.151648 | synonymous-codon | RNF128 | GRCh38.p7 | X:106795671 | CTTTGAAGAAGACGA[A/G]ACTCCTAATCAAGAG | 79589 |
rs61760879 | snp | A/C/T | 0.000208401 | 0.0102061 | missense | RNF128 | GRCh38.p7 | X:106791205 | AGGGAACAGATGAAC[A/C/T]GCCTCTGGAGGAACA | 79589 |
rs66491909 | snp | A/G | 0.377962 | 0.214769 | intron-variant | RNF128 | GRCh38.p7 | X:106732269 | CCAAAACAAAGTATA[A/G]TAATCTCTTTTTGTT | 79589 |
rs67655514 | in-del | -/TG | | | intron-variant | RNF128 | GRCh38.p7 | X:106779358 | GTTACGTGTGTGTGT[-/TG]GTGTGTGTGTGTGTG | 79589 |
rs68040570 | in-del | -/TA | 0.184856 | 0.241363 | intron-variant | RNF128 | GRCh38.p7 | X:106789491 | ATATACATTATACAC[-/TA]TATATAATATAGTGT | 79589 |
rs72618344 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106780664 | TAATTGCTGGCTTTA[A/G]AGGGGTTTTTAAATT | 79589 |
rs73247950 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693564 | AGTTTAGTGTTTTAG[A/G]TATTCTGAGAGAGGT | 79589 |
rs73247951 | snp | A/G | 0.0251071 | 0.109193 | intron-variant | RNF128 | GRCh38.p7 | X:106698802 | CCCATGACACTCAGG[A/G]TAAATTCAAACTTCT | 79589 |
rs73247952 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106701189 | CTTCTTCTTTTATTT[G/T]AATTCTACCTCTTAA | 79589 |
rs73247953 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106702174 | AAATCAAGATATAGT[A/T]CCTCTGGGCACCAGT | 79589 |
rs73247954 | snp | C/T | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106716217 | AAACATTCCTGCCTC[C/T]ATTCTAGCACAGGAC | 79589 |
rs73247955 | snp | A/C | 0.00738971 | 0.0603345 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106726568 | GCCTCAGATCCTATT[A/C]TAACATCGATCCATC | 79589 |
rs73247956 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106749341 | GAAAGGTTTGGAATT[C/T]GCTGGCGCATTATAA | 79589 |
rs73247958 | snp | A/G | 0.370524 | 0.21903 | intron-variant | RNF128 | GRCh38.p7 | X:106783858 | AGAGAGGGAGCAGGC[A/G]CCAGGCTCTTTTAAA | 79589 |
rs73529301 | snp | C/T | 0.0580755 | 0.160203 | intron-variant | RNF128 | GRCh38.p7 | X:106737368 | GTGGAGGATTGGTTC[C/T]ATGACCTCCCGCATA | 79589 |
rs73531104 | snp | A/G | 0.0714214 | 0.174956 | intron-variant | RNF128 | GRCh38.p7 | X:106744792 | TTTTTAAATTCCTCC[A/G]TGTTAATTTCTAATG | 79589 |
rs73531107 | snp | A/G | 0.0580755 | 0.160203 | intron-variant | RNF128 | GRCh38.p7 | X:106746787 | TTCTACTTAATTGCT[A/G]CCTATTTCTAATCTG | 79589 |
rs73531114 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106755604 | GGGATGCAAGGATAG[C/T]TATACATAAATCAAT | 79589 |
rs73531117 | snp | A/C | 0.265183 | 0.249539 | intron-variant | RNF128 | GRCh38.p7 | X:106763410 | TAACTGCAATTGAGA[A/C]CAGTGGAGGGGGAGC | 79589 |
rs73531118 | snp | C/T | 0.316486 | 0.240997 | intron-variant | RNF128 | GRCh38.p7 | X:106763885 | GAAGCACAGCATTGT[C/T]GCTAAGATGTATACA | 79589 |
rs73531123 | snp | A/G | 0.267718 | 0.249371 | intron-variant | RNF128 | GRCh38.p7 | X:106792125 | AACTTTGTATTTCTT[A/G]TATCTAATCTTCAGA | 79589 |
rs73531124 | snp | A/G | 0.0282 | 0.115346 | intron-variant | RNF128 | GRCh38.p7 | X:106794237 | GTTTATCCCTTGCTC[A/G]TATCATCCTAGATTT | 79589 |
rs73638916 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106700991 | AGTGCTGCTCTTTTA[C/G]AAACAATACTTCAGT | 79589 |
rs73638917 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106723153 | TATAAGAAAAGTAGG[A/G]AAAAAAGTACAATGA | 79589 |
rs73638918 | snp | C/G | 0.0363984 | 0.129901 | intron-variant | RNF128 | GRCh38.p7 | X:106728212 | TACCTTATGTATATA[C/G]TTATCCTAGACCCTA | 79589 |
rs73638919 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106750204 | TACACCATGGAAACT[C/G]GCACACACTACACAT | 79589 |
rs74666122 | snp | A/G | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106734356 | CCTTGGTATTTCTTA[A/G]GGTTTGATCACCACT | 79589 |
rs74924729 | snp | A/G/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106762556 | GACCTCAGGTGATCC[A/G/T]CCCCCCATCGGCCTC | 79589 |
rs76060773 | snp | C/T | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106712475 | AAGATCATTAGAGCT[C/T]TGATAAATCACTAAC | 79589 |
rs77221808 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106771772 | CAACTGAGGTACTGG[A/G]TTCATCTCACTGGGG | 79589 |
rs77787177 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106783215 | CATTAAGCTAAATAT[C/T]TTCCACAAAATGATA | 79589 |
rs78179582 | snp | C/G | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106699614 | CATATAGGTCGATCA[C/G]ATCACTCCTCTTCTC | 79589 |
rs78209834 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106754600 | AAGCATCTTCTCTAA[C/T]CACAATGGAATAAAA | 79589 |
rs78381010 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106761382 | TGGTCATTCCTCAAA[A/G]AGCTAAAAACAGAAC | 79589 |
rs78446512 | snp | A/G | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106704455 | AAAAAAAAAAAAAAA[A/G]AGCTGGGGAGTAGTC | 79589 |
rs78564179 | snp | A/G | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106775258 | GTGACTAACTATTCA[A/G]AGGTTATAGTTACAA | 79589 |
rs78976989 | snp | A/C | 0.444444 | 0.157135 | intron-variant | RNF128 | GRCh38.p7 | X:106758204 | CAAATAAAATAAAGT[A/C]CTAGGAGGAAACCTA | 79589 |
rs79273313 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106771803 | GAAATGCAGAAATCA[A/C]CTGTCTTCTGCATCA | 79589 |
rs79462199 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106761177 | ATGATTAGTGATGTT[A/G]AATATTTTTTCATAT | 79589 |
rs111257384 | snp | A/G | 0.0738704 | 0.177421 | intron-variant | RNF128 | GRCh38.p7 | X:106794188 | TACTATAGGATCCTA[A/G]ACGTTTCTTTCATTC | 79589 |
rs111289592 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106756825 | ATGGGAGAAAATTTT[C/T]GCAACCTACTCATCT | 79589 |
rs111348883 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106721797 | AGAGTCAGAACGGCA[C/T]TGGAATCCTTCTTCT | 79589 |
rs111375858 | snp | C/T | 0.018891 | 0.0953342 | intron-variant | RNF128 | GRCh38.p7 | X:106785385 | GATTAAGTTAAGGGT[C/T]ATGAGATGGGGAGAT | 79589 |
rs111384006 | snp | A/T | 0.109295 | 0.206645 | intron-variant | RNF128 | GRCh38.p7 | X:106742179 | ATGGGACTATTTCTG[A/T]TATAGCAAATTTTTA | 79589 |
rs111387150 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106696268 | GTTTTTTAACATATG[A/G]TGATATCAACCCCAA | 79589 |
rs111410677 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106745156 | TTTTGTGCTATATCA[A/G]GTATGTGACCCATTT | 79589 |
rs111572537 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106726063 | AAATGCAGAAGAAAG[G/T]CTTGGTTCTGAGGTG | 79589 |
rs111578359 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106788268 | CCAGCACAATTGATA[C/T]ATATGTATTATATAT | 79589 |
rs111594093 | in-del | -/A | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106782905 | CGGGCTCGGTAATCT[-/A]AAGATCCTAGGTGTA | 79589 |
rs111718178 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106733133 | TATAAATAATCTAGA[G/T]ATTATTTAAAATATA | 79589 |
rs111787787 | snp | C/T | 0.226298 | 0.248874 | intron-variant | RNF128 | GRCh38.p7 | X:106701965 | GTATATAACATGTTA[C/T]GCCTGGAAAATAACT | 79589 |
rs111808333 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106744171 | GAGTTAGTGGGTGCA[C/G]CACACCAACATGGCA | 79589 |
rs111816266 | snp | C/T | 0.225906 | 0.248836 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692938 | TCATCTATTCCTTCA[C/T]CAGCCCTTGGCACAC | 79589 |
rs111819812 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106765864 | TCCTAATGCTATCCC[C/T]CCCAGCCCCCCACCC | 79589 |
rs112196376 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106712922 | TCTCACTCTGCGGCC[C/T]GGGCTGGAAGTGCAG | 79589 |
rs112304071 | snp | A/G | 0.103183 | 0.202348 | intron-variant | RNF128 | GRCh38.p7 | X:106752992 | TTGAGCTTGAAGAGG[A/G]GCTGTTTGAAAATAC | 79589 |
rs112402476 | snp | A/G | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106790430 | TATCATATAGACAAT[A/G]AGGTGCCATCTTGGG | 79589 |
rs112418526 | snp | G/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106748575 | GTATGTGTACACAAT[G/T]GAATACTATACAGCC | 79589 |
rs112497985 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106714479 | CAGTTTCCCCCAGTA[G/T]TATCACCTCGTATAA | 79589 |
rs112639859 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106771000 | TCAGCTGCAGGTCTG[C/T]TGGAGTTTGCTGGAG | 79589 |
rs112666691 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106694437 | GATTCACAAAGAGAG[C/T]TAATGTCCGTTTATC | 79589 |
rs112674475 | snp | G/T | 0.375859 | 0.216008 | intron-variant | RNF128 | GRCh38.p7 | X:106768355 | GGTCCTGGACTTTTT[G/T]TGGTTGGTAGGCTAT | 79589 |
rs112693610 | snp | C/T | 0.100346 | 0.200259 | intron-variant | RNF128 | GRCh38.p7 | X:106765827 | ACCCATTAACTAACT[C/T]GTCATTTATATTAGG | 79589 |
rs112752949 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106743889 | CTGGATTAAGAAAAT[C/G]TGGCACATATACACC | 79589 |
rs112852593 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106743447 | TAACACAGTGAGCCA[A/G]TATTTTCCAAATGAC | 79589 |
rs112942085 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106771230 | GAGGAGGCAGTCTGT[C/T]CGTTCTCAGATCTCA | 79589 |
rs112952199 | snp | A/C | 0.100346 | 0.200259 | intron-variant | RNF128 | GRCh38.p7 | X:106761530 | CATGGAATCCACCTA[A/C]ATGCCCATCAATGGT | 79589 |
rs112978707 | snp | C/T | 0.0590711 | 0.161388 | intron-variant | RNF128 | GRCh38.p7 | X:106713258 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAAGC | 79589 |
rs113031944 | snp | C/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106780035 | TTTAAAATATGGTGA[C/G]TTAAGTACAGAAAAA | 79589 |
rs113088956 | snp | C/T | 0.5 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106789941 | AGTGTCCTAGCCATT[C/T]TCAAATGAGTACTGA | 79589 |
rs113119283 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106712724 | TTAATAACCCTTTGC[C/T]ACAGTTAGTATCATA | 79589 |
rs113254469 | snp | A/C | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106764303 | CTGACCACAATGGCC[A/C]ATGTGTTCCTGAGTA | 79589 |
rs113261913 | snp | G/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106721150 | TTTGTTTTGTTGACT[G/T]CTTCTTCTCTCCACA | 79589 |
rs113344996 | snp | G/T | 0.156045 | 0.231673 | intron-variant | RNF128 | GRCh38.p7 | X:106706714 | AATACTACTTTAAAC[G/T]GCGAAAGATGTATAG | 79589 |
rs113399236 | in-del | -/GTGCTT | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106727970 | AGTGACTTGGTATCA[-/GTGCTT]TTGTTTGCTTCTGAA | 79589 |
rs113408900 | snp | A/G | 0.0173306 | 0.0914601 | intron-variant | RNF128 | GRCh38.p7 | X:106732404 | ATCTTTGTAATCTCT[A/G]TAGAAACCTTTGTAC | 79589 |
rs113443492 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106703008 | AGATGTATATCATAT[A/T]TTTGCCTAAATTTTT | 79589 |
rs113489737 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106755417 | CATTCTATGAGGCCA[A/G]TATTACCCTGATACC | 79589 |
rs113496220 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106750672 | GAAGCTAATTTTACT[A/C]TTTCTGTAGAACCAA | 79589 |
rs113516362 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106732924 | AAGTAAAAATCTTTT[A/T]TAAAAAAAGGAAAAT | 79589 |
rs113522274 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106706192 | ATAGCCTTGGCCAAG[C/G]GTAGCTTTGCAGTGT | 79589 |
rs113608978 | in-del | -/A | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106711086 | AAAATAATTTTTGCT[-/A]AAAAAAAATCACTGA | 79589 |
rs113646021 | snp | C/T | 8.59316e-05 | 0.00655427 | intron-variant | RNF128 | GRCh38.p7 | X:106788035 | ATATCTTCAATAAAA[C/T]AGCTGACCCACAAAA | 79589 |
rs113768583 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106786459 | GTAAACATTATTTCA[A/G]TAGATCATAGACCTT | 79589 |
rs113855644 | snp | G/T | 0.085528 | 0.188279 | intron-variant | RNF128 | GRCh38.p7 | X:106698829 | TTCTTTCCAAGACTT[G/T]ATCCAGCTCTGAATC | 79589 |
rs113866417 | snp | A/G | 0.171252 | 0.237274 | intron-variant | RNF128 | GRCh38.p7 | X:106763522 | GGGTTTTTTGTTTTC[A/G]TTGAGACGGAGTCTC | 79589 |
rs113921251 | snp | A/G | 0.0105399 | 0.0718252 | intron-variant | RNF128 | GRCh38.p7 | X:106713545 | TATTCTGAATGTTCT[A/G]GAGAAATGCTGTCCA | 79589 |
rs113955006 | snp | C/T | 0.169101 | 0.236549 | intron-variant | RNF128 | GRCh38.p7 | X:106751901 | ACCATGAGCCTTGGG[C/T]AAGGCTTCAGGTGTG | 79589 |
rs114132128 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106699269 | CTACAAGGTTTGATG[C/T]TAATCATGTACAATC | 79589 |
rs138001891 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | RNF128 | GRCh38.p7 | X:106784447 | TAGATATATGCTCAG[C/T]GAAACAATAAAAGGC | 79589 |
rs138002378 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106720986 | ATTCTGTCCTTTCTT[C/T]GGGTGCATGAAAGTT | 79589 |
rs138047342 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106707077 | AATTTTGCCTTTTTG[C/T]CTATTTTTATGTATT | 79589 |
rs138188842 | snp | C/T | 0.000136897 | 0.00827224 | missense | RNF128 | GRCh38.p7 | X:106773087 | TTTTTATTATTACGG[C/T]GGCAACTGTGGGCTA | 79589 |
rs138476308 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106733326 | AAATAACTTTTCCCC[C/G]CTCAGTCCCTGGAAG | 79589 |
rs138589993 | snp | A/C | 0.0312828 | 0.12109 | intron-variant | RNF128 | GRCh38.p7 | X:106776557 | GAATGCTAGGAATCA[A/C]TATTGGGAAAGAGAA | 79589 |
rs138667894 | snp | G/T | 0.022522 | 0.1037 | intron-variant | RNF128 | GRCh38.p7 | X:106785278 | TGATTCTAGAGGTTG[G/T]CTGAATAATGGCCTC | 79589 |
rs138754188 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106699875 | TTATCACACATAACA[A/G]GTACTCCATATACCA | 79589 |
rs138757839 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106715452 | TCAGTGGATAATATG[A/G]TTTTACAAAAGAAAG | 79589 |
rs138849878 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106719432 | CGCCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC | 79589 |
rs138946278 | in-del | -/TT | | | intron-variant | RNF128 | GRCh38.p7 | X:106719229 | TACTGCCCATGGGCA[-/TT]TTTTTTTTTTTGAAA | 79589 |
rs138968364 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106722048 | TATAAGGTGAAGTCT[A/G]GTACAGGGGGACTGC | 79589 |
rs139133728 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106758675 | TGCCAAGAACATACA[C/T]TGGGGAAAAGATAGG | 79589 |
rs139264071 | snp | A/G | 0.0665023 | 0.16979 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692656 | TCCCTACTTCTTGTC[A/G]GCTTTTAAACATCTG | 79589 |
rs139273411 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106751409 | CCTAGCCGGAGGAGA[A/G]TTGTCCATCCCTCTG | 79589 |
rs139378713 | snp | A/G | 0.0209675 | 0.10022 | intron-variant | RNF128 | GRCh38.p7 | X:106781644 | TTTATTAAATCACTT[A/G]TCTTGCATCCATATT | 79589 |
rs139609618 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106750235 | TAGGGCTTTCTCCAA[A/C]CCTGAGAGCAGATTT | 79589 |
rs139701141 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106722530 | TGAAATAGAGGAATA[C/T]GGTTGGGTAAAACCA | 79589 |
rs139744531 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | RNF128 | GRCh38.p7 | X:106736110 | ACACTGACTTCATCT[A/G]ATGGTGATAGATTTT | 79589 |
rs139843502 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106733981 | GCTGGAATTACAGGC[A/G]TGAGCCACAGTGCCC | 79589 |
rs139893816 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106711810 | ATGTCTTCTGACACC[A/G]TATGGCAACTGCTTC | 79589 |
rs139921518 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | RNF128 | GRCh38.p7 | X:106696195 | CTGTGATAGTTAACA[C/T]TTACTGGCATTTACT | 79589 |
rs140115610 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106787221 | ACTGGTGAATGGATA[A/C]ACTGTGGTACATACA | 79589 |
rs140137378 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797450 | TTATCACTGTCCATA[C/T]ACTAATTTTTCTCAT | 79589 |
rs140168740 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106702514 | TAAGTACTCTCTGTC[A/G]CTCTCATTTCAGCAG | 79589 |
rs140258491 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106738220 | GATCTTGGGCAAGTT[A/G]TTAACCTAGACCTTA | 79589 |
rs140265268 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106781231 | TAAGAGGTGGAAATA[A/T]TGTGTTACTGGAATT | 79589 |
rs140349717 | snp | A/C | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106783271 | ATCAATGAGATTCCT[A/C]ACCTACTGATACTTA | 79589 |
rs140395832 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106708012 | TTGATGAATGAATAA[A/G]TGAGTGTATGAAAAT | 79589 |
rs140462246 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106782683 | ATTAAATGAGGTAAT[A/G]GATATAAAAAATATA | 79589 |
rs140505190 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106764729 | GTACACATCTGTGAT[A/T]CAAAAGAAATATTTA | 79589 |
rs140530361 | snp | C/T | 4.86997e-05 | 0.00493432 | missense | RNF128 | GRCh38.p7 | X:106694031 | ATAGGTCCAGTTTTT[C/T]TTGGCTCCTTGTAAT | 79589 |
rs140545218 | snp | G/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106790360 | ATAACATCCTTATTT[G/T]TTCGCTATGTAATAC | 79589 |
rs140595114 | snp | A/T | 0.0115877 | 0.0752302 | intron-variant | RNF128 | GRCh38.p7 | X:106712626 | TCTAAAATGTTACTC[A/T]ACTCAGCTATTTTTC | 79589 |
rs140595859 | snp | A/T | 0.0460406 | 0.14457 | intron-variant | RNF128 | GRCh38.p7 | X:106753219 | GAAGACTAAGAGATG[A/T]ACCTATCAAAAATAA | 79589 |
rs140667917 | snp | A/G | 0.00102975 | 0.0226675 | missense | RNF128 | GRCh38.p7 | X:106795684 | GAAACTCCTAATCAA[A/G]AGACTGCTGTTCGAG | 79589 |
rs140679052 | snp | C/T | 0.0245906 | 0.108123 | intron-variant | RNF128 | GRCh38.p7 | X:106740353 | GCAACATTTAAGGTA[C/T]AGAGTACAGGTACCT | 79589 |
rs140750738 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106744962 | ACATAACCACTAGTG[G/T]AAGTCAGAATAGTTC | 79589 |
rs140956990 | snp | C/T | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106718879 | CCAACTACGTGCTAG[C/T]ACCTGGTCACTTATT | 79589 |
rs140981259 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106699156 | AAGTGTTCTCTCTTG[A/C]TATTCTCGCCCCTCT | 79589 |
rs141127795 | snp | A/G | 0.0168099 | 0.0901243 | intron-variant | RNF128 | GRCh38.p7 | X:106733006 | GAGGAACAATATTTG[A/G]GGGAAAAGAAGCATC | 79589 |
rs141216254 | snp | A/G | 0.0480577 | 0.147375 | intron-variant | RNF128 | GRCh38.p7 | X:106768803 | GTTCTTTTAATTGTG[A/G]TATTAGGGTGTCAAT | 79589 |
rs141283670 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106719642 | AATGGCAAGATCATA[G/T]ATATTTATTTTAGAT | 79589 |
rs141376986 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106729979 | TATTGCTGTGAATTA[C/T]GAAGGGGCCACCAAA | 79589 |
rs141420798 | snp | A/G | 2.3491e-05 | 0.00342709 | missense | RNF128 | GRCh38.p7 | X:106791231 | GAACACGTGCAGTCA[A/G]CAAGTAAGCATCATA | 79589 |
rs141457020 | snp | A/G | 6.85252e-05 | 0.00585303 | missense | RNF128 | GRCh38.p7 | X:106694256 | ACAACACTGAGTTTA[A/G]TAATACTAAGAAGCC | 79589 |
rs141655090 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106721629 | CATATATATCCTGGC[C/T]CATATATATCTCCCT | 79589 |
rs141691760 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106701461 | TGTGTGTCGATAGAT[A/G]CAGATAGAGTCACCA | 79589 |
rs141700442 | snp | C/G | 0.00211696 | 0.0324653 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692659 | ATGTTTAAAAGCGGA[C/G]AAGAAGTAGGGAGAA | 79589 |
rs141791035 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106698426 | GGAAGGGTTTAATTA[C/T]AGCAGCAAACTCACA | 79589 |
rs141837397 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106706409 | AACAAAAAAAAACAA[A/G]GGTTTACTTATTCAC | 79589 |
rs142162582 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106741556 | GATAGAATTAGTATT[G/T]AATTTTTTATCTGTT | 79589 |
rs142290170 | snp | A/T | 0.0850455 | 0.187856 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106724994 | ATGTCTCTCTGAACT[A/T]CATTTTTGTAGCTAT | 79589 |
rs142419711 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106716293 | TAAATACCACACCAA[C/T]GCAATAACATGGATG | 79589 |
rs142455205 | snp | A/C/G | 0.00172643 | 0.0293313 | synonymous-codon | RNF128 | GRCh38.p7 | X:106694389 | GACTGGCAATCAGAC[A/C/G]ATACAGATGGCAAAT | 79589 |
rs142551045 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | RNF128 | GRCh38.p7 | X:106762547 | TGAACTCCTGACCTC[A/G]GGTGATCCGCCCCCC | 79589 |
rs142591256 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106766857 | GTTTTAGGTCTAATA[C/T]TTAGGTCTTTAATCC | 79589 |
rs142677826 | snp | A/T | 0.0374181 | 0.131563 | intron-variant | RNF128 | GRCh38.p7 | X:106695305 | TTGATAATTGGTGTT[A/T]TTGCCAAATTTGGCC | 79589 |
rs142678197 | snp | A/C | 0.0142023 | 0.083063 | intron-variant | RNF128 | GRCh38.p7 | X:106776001 | GTAAGAACACATATC[A/C]TCCCTGTTTTTTAGA | 79589 |
rs142692078 | snp | C/T | 0.022522 | 0.1037 | intron-variant | RNF128 | GRCh38.p7 | X:106785279 | GATTCTAGAGGTTGG[C/T]TGAATAATGGCCTCC | 79589 |
rs142712538 | snp | C/G | 0.0787474 | 0.182133 | intron-variant | RNF128 | GRCh38.p7 | X:106709252 | TATCTAAAAGAATAT[C/G]CCCATTGCTCATTTG | 79589 |
rs142759395 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106715497 | GGGGATTTTTTTTAA[C/T]TGGCTATCTGCTAAG | 79589 |
rs142959097 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106749438 | CTGTAGCAACAGAAA[C/T]ACACAACACCACACA | 79589 |
rs142977849 | snp | C/T | 0.100346 | 0.200259 | intron-variant | RNF128 | GRCh38.p7 | X:106764244 | TGCTGGAATTACAGG[C/T]GTGAGCCACCACGCC | 79589 |
rs142983352 | snp | C/T | 0.0317957 | 0.122012 | intron-variant | RNF128 | GRCh38.p7 | X:106733756 | CCCAGGCTGGAGTAC[C/T]ATGGCGTGGTCTCAG | 79589 |
rs143055519 | snp | C/T | 0.00436936 | 0.0465359 | intron-variant, synonymous-codon | RNF128 | GRCh38.p7 | X:106727195 | GCCCGGGGCGCTTAA[C/T]GCCTGTAACCCGCAC | 79589 |
rs143074557 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106738565 | CCTTCTCCCTGGTGT[A/G]TTTCCATTTTAAGCA | 79589 |
rs143166332 | snp | A/G | 0.0266548 | 0.112325 | intron-variant | RNF128 | GRCh38.p7 | X:106719299 | ATCTCAACTCACTTC[A/G]ACCTCCCCCACCCTG | 79589 |
rs143291832 | snp | A/G | 0.226298 | 0.248874 | intron-variant | RNF128 | GRCh38.p7 | X:106704205 | CTTTGGGGGGCCAAG[A/G]AGGGCAGATCACGAG | 79589 |
rs143450595 | snp | C/G | 0.0312828 | 0.12109 | intron-variant | RNF128 | GRCh38.p7 | X:106777557 | GAATCCACTTTTACA[C/G]GGATATTCTTCCACT | 79589 |
rs143543873 | snp | A/G | 0.00023186 | 0.0107646 | missense | RNF128 | GRCh38.p7 | X:106785114 | GAAGGCTTCAACTAC[A/G]CACACTGAAACAAGG | 79589 |
rs143699397 | snp | C/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106787703 | TCCCTTTGTTCTGTT[C/G]CCCTTTTGTTTCAGT | 79589 |
rs143862200 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106740144 | AGTAGGAGAAGGGGA[A/G]TGTGTAAGCAGCATG | 79589 |
rs143952035 | snp | A/G | 0.000189982 | 0.00974449 | missense | RNF128 | GRCh38.p7 | X:106795582 | TTTCTTTTTAAAGAT[A/G]AAAGTCTACAGCTGG | 79589 |
rs143973837 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106707441 | TACTTTATATCATCC[A/G]GTCAATTACCAATCA | 79589 |
rs144023272 | snp | C/T | 0.0204488 | 0.0990265 | intron-variant | RNF128 | GRCh38.p7 | X:106742343 | TTAATGTTTGAAAAG[C/T]TATAAACAAACTCCA | 79589 |
rs144095630 | snp | A/G | 0.0470497 | 0.145984 | intron-variant | RNF128 | GRCh38.p7 | X:106740981 | TATGGGATTGAAAAT[A/G]TTGATGGTATAGAGT | 79589 |
rs144227632 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106713441 | GAGCCCATGAGGTGG[A/C]GGTTGTAGTGAGCCG | 79589 |
rs144375340 | snp | A/G | 0.0338441 | 0.125605 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797287 | ATCTTGCATGAACTG[A/G]GTGAGAACTCACTTA | 79589 |
rs144412626 | snp | A/G | 0.022522 | 0.1037 | intron-variant | RNF128 | GRCh38.p7 | X:106716045 | AAATACTGTTTCCCA[A/G]ATCTGCTCTGCTCTG | 79589 |
rs144555031 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106751159 | TTGTTTTAACATCAT[A/G]TTAAGGAAAGAGGCA | 79589 |
rs144668409 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | RNF128 | GRCh38.p7 | X:106761042 | CAAAGGTCTGATATC[C/T]GAAATCTTTAAGGAA | 79589 |
rs144706993 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106734574 | TAAGGCACCATAGGT[A/G]TTTCCTGGGAATAAA | 79589 |
rs144714463 | snp | A/G | 6.86963e-05 | 0.00586032 | missense | RNF128 | GRCh38.p7 | X:106791112 | AAGTCCCTGTATCCA[A/G]TGAAATATCTAATAG | 79589 |
rs144855229 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106776411 | CTTTCAGAAGAAAAG[C/G]ATTTACTAACTAAAA | 79589 |
rs144885638 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106697086 | CCCTAGCTGGCTTTG[C/T]TCTGAACTTGGAGGC | 79589 |
rs144893407 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106782987 | GAAGATATTTGTGCT[G/T]AAATTAAGTCCCATC | 79589 |
rs144926766 | snp | C/T | 0.0338441 | 0.125605 | intron-variant | RNF128 | GRCh38.p7 | X:106781507 | TTTTTAAGAGGGAGG[C/T]TTGCATCTTGGAACT | 79589 |
rs144926794 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106698074 | CCTAACAATCTTTTC[C/T]GAGCACTGCAGACAT | 79589 |
rs144964366 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106775190 | TTAATATTTGACATT[C/T]GTATATTGTGCGGTT | 79589 |
rs145118766 | snp | G/T | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106719078 | CTTAGCTTAATAGGT[G/T]ATTGTGATTACATAC | 79589 |
rs145146777 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106738891 | CCATCTCCTTACCCT[C/G]ATCTATAGCCCAGCT | 79589 |
rs145213997 | snp | C/G | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106738226 | GGGCAAGTTGTTAAC[C/G]TAGACCTTATTTATC | 79589 |
rs145227979 | snp | A/G | 0.000189982 | 0.00974449 | synonymous-codon | RNF128 | GRCh38.p7 | X:106694293 | TGCGCTGATAGAAAG[A/G]GGTAATTGTACATTT | 79589 |
rs145269486 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106782331 | CATTTGCATTTTTCT[C/T]ATCTCGATGTCCAAC | 79589 |
rs145309939 | snp | A/G | 0.0152462 | 0.0859689 | intron-variant | RNF128 | GRCh38.p7 | X:106740513 | AACAATTGAATAAAC[A/G]GTGGAATTCTCCTTT | 79589 |
rs145592123 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106703031 | AAATTTTTAATGACA[C/T]ATATTCTCAGCATGA | 79589 |
rs145602894 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106766417 | CCATTCTAAGTCGTG[C/T]GAGATGGTATCTCAT | 79589 |
rs145636920 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106705557 | CTTTTCCTCAAAGCA[C/G]TCAATTCAGCAGAGG | 79589 |
rs145670563 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106790725 | TGACTTGGGAAGGTA[C/T]ATAGATGACAATGAT | 79589 |
rs145901235 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106793789 | TACTACAGAAGTGAT[A/G]TTGTGCCCCTTTCAG | 79589 |
rs145901972 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | RNF128 | GRCh38.p7 | X:106733160 | TATACAGGAAGATGT[A/G]CACTGGTTATATGCA | 79589 |
rs145983519 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106762807 | GTTCTTATGTATAAG[A/T]GGGAGCTAAACTTTG | 79589 |
rs146022365 | snp | C/G | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106695419 | GGTGCTTGGAATGTT[C/G]CAAGTTGTACACATA | 79589 |
rs146105128 | snp | C/G | 0.0157677 | 0.0873799 | intron-variant | RNF128 | GRCh38.p7 | X:106723897 | ATAGTTTATCTCTCT[C/G]ATTGTCTCACTAGAC | 79589 |
rs146117399 | snp | C/G | 0.067981 | 0.171374 | intron-variant | RNF128 | GRCh38.p7 | X:106733883 | TTGTTATAGTTTTAG[C/G]AGAGACAGGGTTTCA | 79589 |
rs146386263 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106722208 | TAACTTCCCAACAAG[A/G]AAAGTGTAGTCTTAC | 79589 |
rs146564133 | snp | C/T | 0.0266548 | 0.112325 | intron-variant | RNF128 | GRCh38.p7 | X:106717956 | CTACTCTTTAGTAGA[C/T]TACTCTTAAGCAATT | 79589 |
rs146576686 | snp | A/G | 0.00738971 | 0.0603345 | intron-variant | RNF128 | GRCh38.p7 | X:106758044 | TTGAAAAACCTAAAG[A/G]CCCCACAACAAACTA | 79589 |
rs146617898 | snp | C/T | 0.00135269 | 0.0259714 | missense | RNF128 | GRCh38.p7 | X:106791219 | CCGCCTCTGGAGGAA[C/T]ACGTGCAGTCAACAA | 79589 |
rs146627932 | snp | A/G | 0.00020543 | 0.0101328 | missense | RNF128 | GRCh38.p7 | X:106694159 | ACATGTGAATGTGGC[A/G]TTTATGGATTAGCTT | 79589 |
rs146793883 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106782622 | ACCCTCCACTTGAGC[A/G]TCTCTAAAATGAGGA | 79589 |
rs146804957 | snp | A/G | 0.26916 | 0.249265 | intron-variant | RNF128 | GRCh38.p7 | X:106789385 | ATTATATATTTATGT[A/G]TATATATGTACATTA | 79589 |
rs146846807 | snp | C/T | 0.0271702 | 0.113344 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692469 | TACTATGGGAGGGTA[C/T]GCTAATGAGTAATTG | 79589 |
rs146880125 | snp | A/G | 6.85205e-05 | 0.00585283 | synonymous-codon | RNF128 | GRCh38.p7 | X:106795623 | AGCAAATTCTGTGGC[A/G]GTGGATGTTATTCCT | 79589 |
rs146959940 | snp | C/G/T | 0.0152462 | 0.0859689 | intron-variant | RNF128 | GRCh38.p7 | X:106720915 | TTATGGATATGAAAA[C/G/T]ATTGTTCTTAGTTTT | 79589 |
rs147241722 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | RNF128 | GRCh38.p7 | X:106740285 | GGCACTTAAATGTCA[A/G]TTTAGGTAGGGCTTT | 79589 |
rs147244482 | snp | A/G | 2.31911e-05 | 0.00340514 | missense | RNF128 | GRCh38.p7 | X:106785116 | AGGCTTCAACTACGC[A/G]CACTGAAACAAGGAG | 79589 |
rs147945537 | snp | C/G | 0.0251071 | 0.109193 | intron-variant | RNF128 | GRCh38.p7 | X:106698327 | TCATTTCAGCTGTGT[C/G]CAACGAAGTGGATTA | 79589 |
rs147968762 | snp | C/T | 0.0287145 | 0.11633 | intron-variant | RNF128 | GRCh38.p7 | X:106702249 | AAGTACATTTCATCT[C/T]CCTTTTCTCCATTTT | 79589 |
rs148007449 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106777346 | TGGATAATTAAATTG[A/G]TATAATAATGTAAAG | 79589 |
rs148069056 | snp | G/T | 0.000332111 | 0.012882 | intron-variant | RNF128 | GRCh38.p7 | X:106694421 | TTGGTAAGTAATAAT[G/T]GATTCACAAAGAGAG | 79589 |
rs148077155 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106761136 | ACTTTTCAAAAGAAG[A/T]CATACATGCAGCCAA | 79589 |
rs148223909 | snp | C/G | 2.30078e-05 | 0.00339166 | intron-variant, missense | RNF128 | GRCh38.p7 | X:106727324 | CCATCTGGCTTATGA[C/G]AGAGGGGCGTCTGGA | 79589 |
rs148438665 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106701318 | TTCTATCATTGAGTA[C/T]GTTATTTGATAGAAG | 79589 |
rs148510460 | snp | A/G | 0.0204488 | 0.0990265 | intron-variant | RNF128 | GRCh38.p7 | X:106734727 | AAGGAATAAAATAGT[A/G]CCAAACTCCAGAAGA | 79589 |
rs148539954 | snp | C/G/T | 0.000160102 | 0.00894583 | synonymous-codon | RNF128 | GRCh38.p7 | X:106791164 | TAATCGCAGCGAGAC[C/G/T]GCATCATCTGGATAT | 79589 |
rs148667647 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106741346 | AGTGAACCAGGATGA[C/T]TGTGTTTTAACTTGA | 79589 |
rs148737548 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106724839 | CATTTTACTTGTCCT[G/T]CTCATCAAAACTAAT | 79589 |
rs148899802 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106791290 | ATTGTAGATCATATG[C/T]CTGTATAGTACTCTT | 79589 |
rs149055315 | snp | A/T | 0.043513 | 0.140937 | intron-variant | RNF128 | GRCh38.p7 | X:106730962 | TGCTCTGCCAATTAG[A/T]ATTTTTTAAATCTTA | 79589 |
rs149160677 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106782481 | GCTAGAAAAACATCA[A/G]AAGACAGATGAGTTA | 79589 |
rs149183842 | snp | A/T | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106703853 | TTAGGATTTTGGAGG[A/T]TTAGCAGATTAGGAT | 79589 |
rs149287445 | snp | C/T | 0.0220041 | 0.102557 | intron-variant | RNF128 | GRCh38.p7 | X:106776765 | GATCTCTGACTGATC[C/T]GGACCAAAGGATGGG | 79589 |
rs149363795 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106759628 | ATGAGTTCCTGTCAT[A/T]TGCAACAACACATAT | 79589 |
rs149382752 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106734045 | GATATATTATTTAAA[G/T]AATTATATACTATAT | 79589 |
rs149435608 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant | RNF128 | GRCh38.p7 | X:106722183 | AAACAGGGTGAAACT[A/G]TACTTAAATTAACTT | 79589 |
rs149574657 | snp | A/G | 0.0026455 | 0.0362733 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693255 | GTGCCTGCCATGGGC[A/G]AGGCACTATACTTGA | 79589 |
rs149770262 | snp | C/G | 0.0209675 | 0.10022 | intron-variant | RNF128 | GRCh38.p7 | X:106719015 | CCTTGGAATACAAAG[C/G]CAGCCTTTGCCCACA | 79589 |
rs149774042 | snp | A/G | 0.000189982 | 0.00974449 | missense | RNF128 | GRCh38.p7 | X:106787939 | GGCCCTGATGGAGAT[A/G]GTTGTGCTGTGTGCA | 79589 |
rs149876433 | snp | A/G | 0.0147244 | 0.0845304 | intron-variant | RNF128 | GRCh38.p7 | X:106770105 | TGTAGAGTTTCTGCC[A/G]AGAGATCCGCTGTTA | 79589 |
rs149886609 | snp | C/T | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106696580 | AGCTCACGATTTCAC[C/T]TTCTGTCATCTCATC | 79589 |
rs150034747 | snp | A/C | 0.0261392 | 0.111294 | intron-variant | RNF128 | GRCh38.p7 | X:106781912 | CCCTTAATGCAAGTT[A/C]TACTGTTCTCCTGGG | 79589 |
rs150093023 | snp | G/T | 4.5958e-05 | 0.00479342 | missense | RNF128 | GRCh38.p7 | X:106795690 | CCTAATCAAGAGACT[G/T]CTGTTCGAGAAATTA | 79589 |
rs150134154 | snp | A/C | 0.0409784 | 0.137149 | intron-variant | RNF128 | GRCh38.p7 | X:106715335 | GCGTGCTTATTTTCC[A/C]TCTGTATTTCCTCTT | 79589 |
rs150273244 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106745468 | CTAAGTTCATTTGTG[C/T]GGCTATAAAGAAATA | 79589 |
rs150460553 | snp | A/G | 0.00200679 | 0.0316128 | missense | RNF128 | GRCh38.p7 | X:106694140 | CAACTACACTGCAAT[A/G]GAGACATGTGAATGT | 79589 |
rs150473955 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106755154 | AATAAATTGGAAAAC[A/G]TTGAAGAAATGGATA | 79589 |
rs150523196 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106701610 | TAGGTAAAAGGGACA[A/G]TTTTGGGTTATTTTC | 79589 |
rs150671098 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106787128 | GGAGAAAAAATCTAC[A/G]TTCACATAAAAACAC | 79589 |
rs150733047 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106769117 | TTTACATTTGCTGAG[A/G]AGTGTTTTACTTCCA | 79589 |
rs150778368 | snp | A/G | 0.000569839 | 0.0168699 | missense | RNF128 | GRCh38.p7 | X:106773059 | TATTCAATTTTTTTC[A/G]TTTCTGTGTCCTTTT | 79589 |
rs150861892 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106740055 | ATACCTGAAGAGAAT[A/G]CACATAAGAAGAAGC | 79589 |
rs150895665 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106754441 | TTTTTTTTTTTTTTT[-/T]GTAGCGACAGGGTCT | 79589 |
rs151060315 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106773977 | AAAACAAATCCAACC[C/T]TGGTTAAATTTACTT | 79589 |
rs151104140 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106711223 | TGGAGGGTTGGAGTG[A/G]AAATGCACTTTTGCA | 79589 |
rs151129895 | snp | A/G | 0.0194105 | 0.0965841 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692407 | TTTCAGTTCAATTAT[A/G]TGAATTATTAGGCTG | 79589 |
rs151176115 | snp | A/T | 0.0068637 | 0.0581785 | intron-variant | RNF128 | GRCh38.p7 | X:106742116 | TGTTAATGGTGATTT[A/T]AGTGAAAGATAATGG | 79589 |
rs180737582 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106786031 | TTTGATGCAGTTTCA[A/G]TAAAAATCCTAGTGT | 79589 |
rs180774329 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106707571 | TTGGTGGGATGGGAT[A/G]TACTCCATCTACTTT | 79589 |
rs180775290 | snp | C/G | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106698584 | CAAGAAAACTAATCA[C/G]TTGCATTTCAAATGA | 79589 |
rs180777257 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106796482 | ATTGCTAATGACAGA[A/G]TAAGTAACACTAATA | 79589 |
rs180786338 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106775804 | GATGAAGCTGAGTTA[C/T]GGAAATTTGGCTTCA | 79589 |
rs180794507 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106743551 | ATTTAACCAAGTAGA[A/G]AGAATTCATTGATAT | 79589 |
rs180807164 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106715641 | TGAGAGAATACAACT[A/G]GAGATAAAAGAGAGC | 79589 |
rs180809340 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106761977 | TTAATTTAAAAATTT[A/G]TAATTGACACATAAT | 79589 |
rs180814369 | snp | C/T | 0.00528398 | 0.051128 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692362 | TTACTCTTAAATTGA[C/T]CATAAGCTAATACAC | 79589 |
rs180863176 | snp | C/T | 0.000685926 | 0.0185066 | missense | RNF128 | GRCh38.p7 | X:106791120 | GTATCCAATGAAATA[C/T]CTAATAGTGCCTCCT | 79589 |
rs180878826 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106771631 | GAGTGGGAGTGTCCC[A/G]ATTTTCCAGGTACGG | 79589 |
rs180883368 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106755126 | TGGAGACTACTGGGA[A/C/G]CAGCTATACGCCAAT | 79589 |
rs180896478 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106740104 | TTGAATGCCCCTTTA[G/T]GACCAGCATTATGCT | 79589 |
rs180909492 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106723268 | CATATTGAGTCCGTA[C/T]GCTTTAATATAATTT | 79589 |
rs180914535 | snp | C/G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106713133 | TCGTCCCCCACCCCC[C/G/T]GCCTTGGGCACCCAA | 79589 |
rs180947747 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106732671 | ATACAGGAATAGAGT[A/G]TACACATACTTCAAG | 79589 |
rs180954261 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106695670 | GTTCCTGTGTTTTTA[C/T]GAGTGACTTTCATTT | 79589 |
rs181077136 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106733228 | GTGGATTTTGGTATC[A/G]TTGGGAGGTCCTGAA | 79589 |
rs181421194 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106699505 | CTACCGCCAGCTCTC[A/G]CACTGACTACTGCAA | 79589 |
rs181422386 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106781410 | TGAGGTATATTTGGG[C/T]ACTGTAAAGTTGACA | 79589 |
rs181426900 | snp | C/G | 0.0292288 | 0.117303 | intron-variant | RNF128 | GRCh38.p7 | X:106765750 | ACTTTAAGTTCTAGG[C/G]TACATGTGCACAACA | 79589 |
rs181427854 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106792324 | AGTCTTTTAAAAAAC[A/G]ACATTCCAATCTACT | 79589 |
rs181428882 | snp | A/G | 0.0204488 | 0.0990265 | intron-variant | RNF128 | GRCh38.p7 | X:106715898 | GAGATTGAATAAAAA[A/G]CCTACAATGACAGTC | 79589 |
rs181430383 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106746844 | GCAGAATGAAAATGC[A/G]TGAAACTCTAGCCAT | 79589 |
rs181484669 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106739786 | AGGAAATTTAATATA[C/T]TCAGGTACTAGAATG | 79589 |
rs181520572 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106782688 | ATGAGGTAATGGATA[C/T]AAAAAATATATTTTA | 79589 |
rs181520803 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106765803 | ACATGTGCCATGTTG[G/T]TGTGCTGCACCCATT | 79589 |
rs181543033 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106696180 | GCATAATGATCATAA[C/T]TGTGATAGTTAACAT | 79589 |
rs181547567 | snp | C/G | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106713293 | GCGGGTGGATTGCTT[C/G]AGCTTAGGAGTTGGA | 79589 |
rs181564468 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106771806 | ATGCAGAAATCACCC[A/G/T]TCTTCTGCATCACTC | 79589 |
rs181580372 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106707052 | TTACATACATAGTTC[A/G]GGTCATGCTAATTTT | 79589 |
rs181584035 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106740766 | GGACAAAAGGAACAC[C/T]GTAATTTCTAATGAT | 79589 |
rs181625309 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106762563 | GGTGATCCGCCCCCC[A/G]TCGGCCTCCCAAAGT | 79589 |
rs181628174 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106785369 | AGGACTTTGCAGATA[C/T]GATTAAGTTAAGGGT | 79589 |
rs181634676 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106744321 | ATGCAGAAACAGCTA[C/T]GAAGATTCAGCCATC | 79589 |
rs181642344 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106729214 | CACTCTACATACATA[C/T]TACTTATACTTTATT | 79589 |
rs181645716 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106767062 | AGGGCTCTATTCTGT[C/T]CCATTGATCTATATC | 79589 |
rs181648143 | snp | A/C | 0.0792336 | 0.182589 | intron-variant | RNF128 | GRCh38.p7 | X:106704206 | TTTGGGGGGCCAAGA[A/C]GGGCAGATCACGAGG | 79589 |
rs181653321 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106747419 | AGCGCTATGTTTGTT[A/T]AGAAAAATAGGATGA | 79589 |
rs181659556 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106770628 | ACTTCTCTACACTGT[G/T]TATTCTAGTTAGCCA | 79589 |
rs181721546 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106790406 | TATACCTAAAACCAG[A/T]CATATTTATATCATA | 79589 |
rs181725865 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106743273 | AAACTTTTATCTACT[A/G]TGTAAGCATAACTTC | 79589 |
rs181730603 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725718 | CTCTGTGAGGTAGGT[A/G]CAATTATTATCCCCC | 79589 |
rs181732556 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797186 | AGTTTACAGTCATGA[C/T]GGAAGGCTAAGTGGA | 79589 |
rs181753195 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106733683 | AGCATTGGGGGGATT[A/T]GTCATTTTATTCTTT | 79589 |
rs181793161 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106716474 | ATAGCATGAGGGAGT[G/T]TTTGTGGTAATGAAA | 79589 |
rs181793175 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106737039 | CAGTTTCTGTGTCAT[A/G]TTGACCAAAGTTCTG | 79589 |
rs181998853 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106776443 | AGACAGATTAGAAGG[A/G]AATCATCTTCCAAGA | 79589 |
rs182027307 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106774257 | TTGAAGCAATCAATA[A/G]TACTTCCACATCTTC | 79589 |
rs182027740 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106795280 | TTAACAGCTTGTTAT[A/C]TTTAAGGTAAGGAAG | 79589 |
rs182034369 | snp | A/G | 0.221969 | 0.248424 | intron-variant | RNF128 | GRCh38.p7 | X:106704218 | AGAAGGGCAGATCAC[A/G]AGGTCAGGAGATCAA | 79589 |
rs182038427 | snp | A/G | 0.0068637 | 0.0581785 | intron-variant | RNF128 | GRCh38.p7 | X:106700369 | TTCTCCCACTAGATT[A/G]TAAGTTCCAGGAAGA | 79589 |
rs182039193 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106720640 | ATAATGTTCTCCCTA[C/T]GTATGTGTAGAGGTA | 79589 |
rs182039421 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106760564 | AATTAGTCCAGCCAT[A/G]TTGGAAAACAGTATG | 79589 |
rs182040409 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106750447 | AGTTAGTCAAACTTA[C/T]CATTAATGGGGATAG | 79589 |
rs182056753 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106719952 | ATTAAAAACATTTTC[C/T]TATCCCACTTTCCCC | 79589 |
rs182111053 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106769049 | GTTTCTTAATCCTGA[A/G]TTCTAGTTTCATTGC | 79589 |
rs182118736 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106751894 | AGTACTCACCATGAG[C/T]CTTGGGCAAGGCTTC | 79589 |
rs182127022 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106737825 | TTCAATCAAATTCTT[C/T]CATCACCAGTTCATT | 79589 |
rs182131784 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106721149 | TTTTGTTTTGTTGAC[C/T]GCTTCTTCTCTCCAC | 79589 |
rs182152419 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106700816 | GTTATTCTGTAGCTT[G/T]CTTTAGCTACTCAAC | 79589 |
rs182158388 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106717383 | AAAAAAATTAATATC[A/T]CTTCTCTTTTCTAGT | 79589 |
rs182261535 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106704574 | AAGGAGAAGTCGTGT[A/C]CTCATGATAAGACGG | 79589 |
rs182274694 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106697015 | AGGTTTCTTGGGATA[C/T]GGGACTCTTAATGTT | 79589 |
rs182301731 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106772415 | TTTGGGTTTGTAAAC[A/G]TTGTTTGGCTCAAAT | 79589 |
rs182308032 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106758552 | ACACAGTTATAGTAA[C/T]CAAAGAAGCATGGTA | 79589 |
rs182308626 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106785926 | GATAAATCAAAGAAG[A/T]TCTAAATAAATGGAA | 79589 |
rs182311285 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106695460 | GTTTGGTACTAATAT[A/T]TGAAAACCAAACTGC | 79589 |
rs182313137 | snp | G/T | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106741543 | CCAAGGTCTATAGGA[G/T]AGAATTAGTATTTAA | 79589 |
rs182317795 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106751401 | AGACCAGCCCTAGCC[A/G]GAGGAGAATTGTCCA | 79589 |
rs182382685 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106701611 | AGGTAAAAGGGACAA[G/T]TTTGGGTTATTTTCC | 79589 |
rs182388695 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106718315 | TCAATTTCTGCCCTC[A/T]TTTTCCCCCTCTCGA | 79589 |
rs182435153 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106778148 | TAGTTAAGTTTTGGG[A/G]GTGTCAAAAGCTATA | 79589 |
rs182456736 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106745012 | ATATAATATTTCTAA[G/T]AATTGTTTACCTATG | 79589 |
rs182519297 | snp | A/C | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106778988 | GGTGTGTTCACATGT[A/C]TGTATCTATTTCTGC | 79589 |
rs182527127 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106764191 | AGGATAGTCTTGATC[G/T]CCTGACCTCGTGATC | 79589 |
rs182539282 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106709301 | TTGGATATCCTATTA[A/T]TACTTCTCTGAAGAA | 79589 |
rs182575168 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106768022 | TGGATTACATTTATT[G/T]ATTTGCTTATGTTGA | 79589 |
rs182582782 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106712566 | CTACTTTTTGCAAGA[C/G]AGAAGTTCCCTTATG | 79589 |
rs182590858 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106737388 | CCTCCCGCATATACT[A/G]AAATCCACAGATGCT | 79589 |
rs182597088 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106765923 | CCACCCTGTGTCCAA[A/G]TGTTCTCATTGTTCA | 79589 |
rs182615207 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106733862 | TGTGCTAACACACCC[A/G]GCTAATTGTTATAGT | 79589 |
rs182662004 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106766015 | AGAATGATGGTTTCT[A/G]GCTTCATCCATGTCC | 79589 |
rs182662464 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106748510 | GCACTATTTACAATA[C/G]CCAAGATATGGAATC | 79589 |
rs182676924 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106734169 | TGACTGAGAGTTGGG[G/T]ATTGAGCCTCTCTTT | 79589 |
rs182694473 | snp | C/T | 0.0312828 | 0.12109 | intron-variant | RNF128 | GRCh38.p7 | X:106763724 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGATC | 79589 |
rs182711286 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106730819 | TGAGGGCTGTAAAAA[A/C]AAAAAGTGAATGAAC | 79589 |
rs182752187 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106784098 | ATGTATATTATATTC[A/G]CTACTTCAATTCATA | 79589 |
rs182787428 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106693947 | AGTGGACAATGGTGA[C/T]TGATAGTTGGAAATA | 79589 |
rs182869631 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106782897 | TTAGATGTCGGGCTC[A/G]GTAATCTAAAGATCC | 79589 |
rs182879132 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106724405 | CTCTAAACTTCAGAT[C/G]TGATTCTATTACTCC | 79589 |
rs182883212 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106747691 | AAATATCAAAACCAA[C/T]ACAAAACAATTTGTT | 79589 |
rs182888880 | snp | A/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106786814 | ACAATTCACCAAAAA[A/T]ATATATATATGAATG | 79589 |
rs182938832 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106757713 | ACAATGTGCACATGT[A/T]CCCTAAAACTTAAAG | 79589 |
rs182945152 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106740931 | TTATCAAATAGTCCT[A/G]TCAGATTCTGAACAG | 79589 |
rs182950415 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106724074 | ATCGACATATCTAAA[A/G]TGAACTCATCTCTCC | 79589 |
rs183066136 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | RNF128 | GRCh38.p7 | X:106708225 | ATTTGATGTCTCATC[C/T]TTAGCTGGCAGTTGG | 79589 |
rs183108756 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106708927 | TTGAATTAATACTTC[A/C]GTTGCTTTTATGCAA | 79589 |
rs183214165 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106723439 | GGGCATGGTGGCACG[C/T]GCCTGTAATTCCAGC | 79589 |
rs183221312 | snp | A/T | 0.0121112 | 0.0768695 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692800 | GGACCTTGGACTACC[A/T]TTGTCCCTACCTTCC | 79589 |
rs183243795 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106705345 | TGATCTGTTTGTTAT[C/G]ACTAATGCTAATTAC | 79589 |
rs183308752 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106748732 | TGAATCTCATGAAGA[C/T]AGAGAGTAGATTGGT | 79589 |
rs183310144 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106772061 | GTCATATAAACTAGA[C/G]GGAATATAAACCTTG | 79589 |
rs183367032 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106793435 | AATACAAAGAATGCC[C/T]ATATACCATTCACCC | 79589 |
rs183379188 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106704609 | TGGTTGAGTCAGGAA[A/G]CACAGGGAACCCACA | 79589 |
rs183437243 | snp | C/G | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106769674 | TGATGGGTCTTGATT[C/G]TTTATCCAATTTGCC | 79589 |
rs183462918 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106738077 | TTGCTCTGTTTTTAT[G/T]TCAACCTATTGTACC | 79589 |
rs183528035 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106777286 | TTAAATTGCTCTGTG[C/T]AAGTCTATCACAAAG | 79589 |
rs183529421 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106738867 | CTGGTTTATTAAAGG[A/T]TAGCTTGACCATCTC | 79589 |
rs183537459 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106721579 | AGGGTAGGCCTTTGT[A/G]GTAGGATTTGAAGAA | 79589 |
rs183538954 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106763360 | CATGATTCTGAGGTT[A/G]CTAAACTAGGTGACC | 79589 |
rs183540078 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106792987 | GGTGATAGTTGATTT[A/G]CATAACTTTGTAAAT | 79589 |
rs183540647 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106744710 | GTGATCCACCCACCT[C/G]GGCCTCCCAAAGTGC | 79589 |
rs183542505 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106766165 | ATTGTGAATAGTGCC[G/T]AAATAAACATACGTG | 79589 |
rs183551929 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106735580 | ATAATCAGAAAAATT[C/T]GTAGTTTTAAAGAAC | 79589 |
rs183552734 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106718938 | GATCAAGTTTGAGTC[C/T]TGTGCAGCTGCCACT | 79589 |
rs183645359 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106696801 | AGCCAAAGACCGCTA[A/G]CAACAGACCTGTAGT | 79589 |
rs183657984 | snp | A/T | 0.017851 | 0.0927731 | intron-variant | RNF128 | GRCh38.p7 | X:106770093 | TCTCTTCTGATTTGT[A/T]GAGTTTCTGCCGAGA | 79589 |
rs183672811 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106739156 | CTTCCTTCCTTCCTT[A/C]TTTCTTTCTGACTTT | 79589 |
rs183677094 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106722346 | CTCAAACATATATAC[A/G]TGCAGATCCCCTGGG | 79589 |
rs183699825 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106753035 | GACAAAAAAAGAATA[A/C]AATAGAATGAAGCAC | 79589 |
rs183713143 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106721317 | GTTTGTCCCAAGTTG[C/T]GCTTTGCCATTCATT | 79589 |
rs183764069 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106703806 | AAGTGAGAGAGTTAT[A/C]GGATAACCAGTCAGA | 79589 |
rs183778119 | snp | C/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106736351 | GTTGCTTTGGTACCA[C/T]TTATTTTCCTCTTAG | 79589 |
rs183784311 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106719148 | GAGCCCCAGCCTTAT[C/T]AGAAATTATCCAGTT | 79589 |
rs183871253 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106713851 | TTCATCAAATTTTCA[G/T]AGGTAACTCTGACCT | 79589 |
rs183903648 | snp | G/T | 0.00738971 | 0.0603345 | intron-variant | RNF128 | GRCh38.p7 | X:106698747 | AAGTGGCTTTTTAGA[G/T]AAAATAAATCTCATT | 79589 |
rs183919378 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106715800 | TCCAAGTTGTATACC[C/T]ACCTGGACAGAGAGC | 79589 |
rs184015882 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106787075 | AATACACTTACCATA[A/G]CACCTAGCAATCTCA | 79589 |
rs184040298 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106753600 | ATGGGAAGGGAGTAA[A/G]AACTTATCAATAATA | 79589 |
rs184074962 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106730052 | CTTCACTCACTCTCA[C/T]AGGGGCCTGCACTTG | 79589 |
rs184133326 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106781057 | TGAGAAGTGTCTTGC[A/G]TGAGAAAATCAAGAA | 79589 |
rs184146996 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106746390 | TTTACATTTTAACAC[A/G]TTAATATTAAATGTG | 79589 |
rs184182563 | snp | G/T | 0.0168099 | 0.0901243 | intron-variant | RNF128 | GRCh38.p7 | X:106769884 | CTTTTGCAGTGGCTG[G/T]TACCAGTTGTTCCTT | 79589 |
rs184203334 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106773719 | TATTAATAGTTTCTA[A/C]CATATTATAACAGTG | 79589 |
rs184206248 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106759750 | TTAAACAGTTGGAGA[C/T]AGATATCAGAAGGAT | 79589 |
rs184214646 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106742720 | GGGTAAAACTGCTGT[C/T]ACCTTAACACAAATT | 79589 |
rs184223285 | snp | G/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725152 | CCATTTCTCAGAGGT[G/T]GTTGGTCCTACCCAT | 79589 |
rs184264748 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106784760 | AATAGGAAGATTGCT[C/T]TGAAAATTCATAGTA | 79589 |
rs184269763 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106766711 | TGTGCAGAAGCTCTT[C/T]AGTTTAATTAGATCC | 79589 |
rs184278759 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106765443 | AAAACTGTGAATACT[A/G]TTTTAATATTTTACT | 79589 |
rs184278805 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106749894 | TGGGCAACAGAGCGA[C/G]ACCTTGTTTCAAAAA | 79589 |
rs184284428 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106736755 | TTTTATTACAAATAT[G/T]GGTTAAATAATAATT | 79589 |
rs184288963 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106719678 | ATCTGATTTGTTAGG[C/T]TTTCATCTAATGGAA | 79589 |
rs184299866 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106732815 | TGCTGGGGTGTTTTA[A/T]TTTTTTGATCTTTTA | 79589 |
rs184303582 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106697580 | ACATTTCTGTGCCTC[C/T]GCATCCCTTATAGGT | 79589 |
rs184311310 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106714980 | TTAGGTTGTTTCCAA[G/T]ATTTGGCAATTATGA | 79589 |
rs184336651 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106745672 | TTCTTTGATGAGGTA[A/C]ACTGATAGTAAATAC | 79589 |
rs184347725 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106731300 | AGGAAAAAGATCTTT[A/T]GGTCCTCCTATGTTT | 79589 |
rs184441064 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106695379 | TATGAAAAGGAGAAA[A/G]TCAAACTTATGTTAA | 79589 |
rs184445231 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106711952 | ATTCCCAGAATGAAT[A/G]AGATCAGTAAGTTCA | 79589 |
rs184469747 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106695461 | TTTGGTACTAATATT[A/T]GAAAACCAAACTGCT | 79589 |
rs184592754 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106706084 | ACCTGATGCATTACC[A/C]CATGATACCTCCACG | 79589 |
rs184607582 | snp | A/G | 0.078261 | 0.181675 | intron-variant | RNF128 | GRCh38.p7 | X:106704197 | TCCCAGCACTTTGGG[A/G]GGCCAAGAAGGGCAG | 79589 |
rs184666261 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106795360 | AATAAGCACATGTAC[A/G]TGAATCAAAAAAGCA | 79589 |
rs184668678 | snp | C/T | 0.0450304 | 0.143134 | intron-variant | RNF128 | GRCh38.p7 | X:106774413 | TCAAGGACATCACTC[C/T]AGAAATTTTCCTCTC | 79589 |
rs184680477 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106760597 | GAGTTTTTAAAAATG[A/T]TAGAAATACAATTAC | 79589 |
rs184721927 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106770617 | GTCATTTAAGGACTT[C/T]TCTACACTGTTTATT | 79589 |
rs184727031 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106709718 | TGCCCAACTAATTTC[A/G]TATTTTTAATAGAGA | 79589 |
rs184750059 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106739590 | CTAATATGGTAGCTT[G/T]TATATCAGGTTTATG | 79589 |
rs184795474 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106754664 | TACAAATACATGGAG[A/G]TAAACAGTATGCTCC | 79589 |
rs184798859 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106780414 | ACTAACTAGAGCGAA[G/T]GCAGCTTTTGATTAG | 79589 |
rs184801655 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106765111 | GTAAATGAGAACAAG[A/G]TGAGTCATTAATCTC | 79589 |
rs184853174 | snp | A/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106789917 | AATGAACAAAGTCTT[A/T]GGTCAGGTAGTGTCC | 79589 |
rs184869701 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106754025 | TCAACACCCTACTTT[A/C]AGCATTGGACAGATC | 79589 |
rs184881068 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106794363 | TTTTCTGTAAGGGGC[A/C]ACATAGTAAATATGT | 79589 |
rs184882332 | snp | C/T | 0.000140081 | 0.00836783 | synonymous-codon | RNF128 | GRCh38.p7 | X:106791221 | GCCTCTGGAGGAACA[C/T]GTGCAGTCAACAAGT | 79589 |
rs184894216 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106733996 | GTGAGCCACAGTGCC[A/C]AGCTTATCATTTTAT | 79589 |
rs184896518 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106771655 | GGTACGGTCTGTCAC[A/G]GCTTCCCTTTGCTAG | 79589 |
rs184901047 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106759003 | AGAAGAGACTACCCA[C/T]AGAATGGGAGAAAAT | 79589 |
rs184905584 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106755135 | CTGGGAGCAGCTATA[C/T]GCCAATAAATTGGAA | 79589 |
rs184910674 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106740440 | AAGGTCATGTCCCAG[C/T]TTCATTGTAAGTCTA | 79589 |
rs184921932 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106724763 | TTATCCACTACTACC[C/T]TGTCATATCTCCATC | 79589 |
rs185009682 | snp | C/T | 0.0016622 | 0.0287808 | intron-variant | RNF128 | GRCh38.p7 | X:106772866 | AATTGGGTTATTATA[C/T]TAAGAATGTTTCACC | 79589 |
rs185023082 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106742050 | ATTAGTAGCCATGAG[A/G]AGAATGAATTAGAAG | 79589 |
rs185107470 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106794811 | AATCCCACACTACAG[G/T]GTTCATTCTAGCCTC | 79589 |
rs185163158 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106706887 | ATGCTCATGAAGTCA[A/T]CCTTGTTTTCAGTTC | 79589 |
rs185384534 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106702457 | GTGTGTAAATACACA[C/G]AGAACAATGCCTGAG | 79589 |
rs185412897 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106697721 | GCCTCCCTACTAAGA[C/G]TGTTATTTTTCTGAA | 79589 |
rs185532355 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106743301 | TTCCCAATACTTAGA[C/T]TTTTCTAATGGGATC | 79589 |
rs185533963 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106786204 | AGTCAAGATAGTGTC[A/G]TATTGGAAAAAGGAT | 79589 |
rs185538231 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106769289 | ACTTACTGTCTCGTT[C/G]ATCTGTCTAATGTTG | 79589 |
rs185538499 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106766346 | AACAGTTAAAGGAGT[C/T]CCTATTTCTCCACAT | 79589 |
rs185543968 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106715320 | ATTTAACATCTTTTC[A/G]CGTGCTTATTTTCCA | 79589 |
rs185544711 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106752379 | TTTGAGAGAAAGTAA[A/G]GGAAGAGAACAACAC | 79589 |
rs185552970 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106737999 | ACAAAAGAATTGACT[G/T]ACTTTGAGTAATGTA | 79589 |
rs185558801 | snp | A/G | 0.0115877 | 0.0752302 | intron-variant | RNF128 | GRCh38.p7 | X:106712853 | TGACTACCTCCTAAT[A/G]TTCTTGAAGTTATGA | 79589 |
rs185582594 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106695804 | TGGGTTTCCTTTTGC[A/G]TGAACACATTCTACT | 79589 |
rs185637892 | snp | A/T | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106790662 | TATATTTGGTAAATG[A/T]AAAAAAGGCCTATTT | 79589 |
rs185650475 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106781716 | ATTGAAAATACTCAA[A/G]TTTTCTTTTAAACAC | 79589 |
rs185664454 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106765786 | GTTTGTCACATATGT[A/T]TACATGTGCCATGTT | 79589 |
rs185667344 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106784539 | CTTAATACCAAACAG[C/T]GTAAAGGTTGGTACT | 79589 |
rs185672695 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106746925 | GAATCTGTAACTACT[A/G]TATACATTTGTTGTA | 79589 |
rs185673951 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725958 | TAGGCGAGTCAGGCT[C/T]CTTTCAGTTAGTGGG | 79589 |
rs185677113 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106733345 | AGTCCCTGGAAGATA[C/T]GTGTTTTCAATACAG | 79589 |
rs185688756 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106732210 | TCCTCATCTTTGAAG[C/G]CTTTCTTAATTCTTT | 79589 |
rs185711419 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106699800 | ACATTTTCTCCAACA[A/C]GTGAAGCTTTTCCTG | 79589 |
rs185719425 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106715903 | TGAATAAAAAGCCTA[C/T]AATGACAGTCCACTG | 79589 |
rs185727999 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692810 | CTACCATTGTCCCTA[C/T]CTTCCTTTTGACCTG | 79589 |
rs185762633 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106747821 | TGGCCATAATAGTAG[A/G]TATATACAATTCATT | 79589 |
rs185774742 | snp | A/G | 0.01368 | 0.0815649 | intron-variant | RNF128 | GRCh38.p7 | X:106770681 | TTTTTACTTCTTTGC[A/G]ATGGGTTCGAACATC | 79589 |
rs185793134 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106723396 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79589 |
rs185813735 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106746052 | GGAAATGTTTGTTAC[A/G]TTGGAACTCTTTACA | 79589 |
rs185902528 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106776652 | GGGTAATGACCTTCC[A/G]TTTTTAGCTGTAGAA | 79589 |
rs185902716 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106762575 | CCCATCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 79589 |
rs185913392 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106744513 | GGAGTCTCACTCTGT[C/T]ACCCAGGCTGGAGTG | 79589 |
rs185923987 | snp | A/C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106729498 | AAATAATGTACAAAT[A/C/G]TATGATTGTGCAACT | 79589 |
rs186094228 | snp | C/T | 0.00211696 | 0.0324653 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692497 | TTGGCAGCTATGATA[C/T]GATAGCAAGGTTCAT | 79589 |
rs186123964 | snp | C/T | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692228 | CAACATTTATAATAA[C/T]AATAATAACATTTCT | 79589 |
rs186133273 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106707349 | ATGCCAAAATGTGCC[G/T]TCCTCTAACTTTCAC | 79589 |
rs186146120 | snp | C/T | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106783069 | TTGATTATCACCTCT[C/T]TTCCTTTTTAGGGTC | 79589 |
rs186213366 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106751557 | GAACCAGAGGACTTG[C/T]GGTGCATATGGCCAA | 79589 |
rs186223158 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106737808 | TACTTTCATAGGTGT[A/G]TTTCAATCAAATTCT | 79589 |
rs186228496 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106720658 | ATGTGTAGAGGTAGT[A/G]TAGCAGAATGAAAAC | 79589 |
rs186236378 | snp | A/T | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106707640 | TGGGGGCCAGTCACC[A/T]GTGTGATGTGCGGTT | 79589 |
rs186243923 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106696418 | AACATAAGGAATCAA[A/G]TGTGGATATGAAAAC | 79589 |
rs186251379 | snp | G/T | 0.221574 | 0.248379 | intron-variant | RNF128 | GRCh38.p7 | X:106704590 | CTCATGATAAGACGG[G/T]TTTTGGTTGAGTCAG | 79589 |
rs186255841 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106713606 | ATTTCTGTGTTGAAT[A/T]TGTAGCCACGAGCCA | 79589 |
rs186274606 | snp | C/T | 0.0850455 | 0.187856 | intron-variant | RNF128 | GRCh38.p7 | X:106704426 | GACAGAGCGAGACTC[C/T]GTCTCAGAAAAAAAA | 79589 |
rs186284575 | snp | A/G | 0.00528398 | 0.051128 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797466 | ACTAATTTTTCTCAT[A/G]TAATATGTCTGGATT | 79589 |
rs186285083 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106765937 | AGTGTTCTCATTGTT[A/C]AATTCCCACCTATGA | 79589 |
rs186286371 | snp | A/T | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106771843 | GGAGCTACAGACTGG[A/T]GCTGTTCCTATTCGG | 79589 |
rs186307910 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106740783 | TAATTTCTAATGATC[A/G]TTTGTATAAATTTTC | 79589 |
rs186377435 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106708609 | AAAGAAACTCTTTTA[A/C]GTAGTATATAGAAGC | 79589 |
rs186377459 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106777398 | ACTGGATGAATTGTT[A/C]CTTTGAACCTGTTTC | 79589 |
rs186382797 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106739830 | ATTTTTTGGTACCTA[C/T]ATGATACCAAAAGTC | 79589 |
rs186386642 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106723178 | CAATGAGCACCCATA[C/T]ACCCACCATCTAGAT | 79589 |
rs186408161 | snp | A/G | 0.0100156 | 0.0700533 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797030 | AACTATCTGTATTAG[A/G]ATGTTTCTTGTGTCA | 79589 |
rs186430268 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106792746 | CCTACTGTTGGCTTC[C/T]ATAGAACTTCGATCA | 79589 |
rs186448812 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106755662 | GAAGGACAGAAAGCA[A/T]ATAATTCCAATTGAT | 79589 |
rs186464234 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106762470 | AGGCATGCACTGCCA[C/T]GCCTGGCTAATTTTG | 79589 |
rs186476217 | snp | G/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106728034 | AACAGGTGACTAACG[G/T]TCTTGAAAAAGAAGA | 79589 |
rs186486945 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106723582 | AAAATATATATATAT[A/G]TATGTATGTATGTAT | 79589 |
rs186487936 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106782730 | AACTGTATATTGTAA[A/G]GAAATGGTAGGAGTA | 79589 |
rs186548345 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106785474 | AGAGAGGGAGATTTG[A/G]CCACAGTACAGTAAG | 79589 |
rs186574382 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106750555 | CAACCTCAGAAATCC[A/G]GTGCATAGCCAGGAT | 79589 |
rs186590389 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106720243 | TTCTCAGCAATCTGT[A/G]ATCCTCTCAATCACC | 79589 |
rs186644147 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106776301 | GCATGTGTTGGATTA[A/G]ACATTGGCAAGTGAA | 79589 |
rs186655632 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106721264 | TATACCTATGTTGTC[A/G]AGCTGTGTATCCAGC | 79589 |
rs186661646 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106743597 | CTTGCACATAGTATT[C/T]AAGAAACTACCATTT | 79589 |
rs186795388 | snp | C/T | 0.00896606 | 0.0663524 | intron-variant | RNF128 | GRCh38.p7 | X:106767387 | TGTCCTCTTTTATTT[C/T]GTTGAGCAGTGGTTT | 79589 |
rs186803314 | snp | A/G | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106701250 | GGCTACAATAGTGAT[A/G]ACAGTATACATCCTT | 79589 |
rs186808818 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106717684 | AATTATAATACCTCT[A/G]TGCCCAATGATAGTT | 79589 |
rs186818736 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106737115 | TCTTAATCTTTGAGG[A/G]TCTCAGATGTTGGCT | 79589 |
rs186926836 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106697066 | AAATTGTGACAAGTT[A/G]GCCACCCTAGCTGGC | 79589 |
rs186928404 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106766080 | ATAGTATTCCATGGT[A/T]TATATGTGCCAAATT | 79589 |
rs186936647 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106714536 | ATTGGAGTTGATACA[A/C/G]TCCACCCACCTTACT | 79589 |
rs186938819 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106748589 | TGGAATACTATACAG[C/T]CTTAAAAAATGAAAT | 79589 |
rs186946898 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106734170 | GACTGAGAGTTGGGG[A/T]TTGAGCCTCTCTTTC | 79589 |
rs186953532 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106772643 | AATACTGTTGAATTA[C/T]AGATAGTTAATCTGA | 79589 |
rs186955578 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106793481 | TAACATATAACCATA[C/T]ACAATTATCAAAACC | 79589 |
rs186969883 | snp | A/C | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106758825 | ACCTCAAAATATGAA[A/C]CTACTAAAAGAAAAC | 79589 |
rs187066769 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106718383 | AAAAGACTTTCTGTG[A/G]CTCTAGAGTTGGCAG | 79589 |
rs187075876 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106730856 | GTTTAATTAATGATT[A/T]GGGGGTCTCCAATGG | 79589 |
rs187078785 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106710073 | TTCATATAAATTTTA[A/T]ATACTGCATAAATTG | 79589 |
rs187080632 | snp | G/T | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106700455 | TGGTCTTCACTATTT[G/T]CTCAATGAATAAAAG | 79589 |
rs187114665 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106704207 | TTGGGGGGCCAAGAA[A/G]GGCAGATCACGAGGT | 79589 |
rs187142501 | snp | G/T | 0.0142023 | 0.083063 | intron-variant | RNF128 | GRCh38.p7 | X:106768721 | TCTATCTCCTTCTCT[G/T]CTGCTCTGATCTTAG | 79589 |
rs187187433 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106788426 | AATATATAATATATA[A/T]TATATATAATATTAT | 79589 |
rs187198193 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106770114 | TCTGCCGAGAGATCC[A/G]CTGTTAGTCTGATGG | 79589 |
rs187199884 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106753812 | AGCTATACTTATATC[A/T]CACAATATAGATTTC | 79589 |
rs187204869 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106715089 | GAAATTGGTGAGTTG[A/G]ATGTTAGTTTTATAA | 79589 |
rs187268396 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106716623 | AAACGTTAGGAAAAA[A/T]TCATACCAGCTAGGC | 79589 |
rs187296807 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106785951 | ATGGAAACATATACC[A/C]TGTTCATGGGTCAGA | 79589 |
rs187297864 | snp | A/T | 0.0110639 | 0.0735497 | intron-variant | RNF128 | GRCh38.p7 | X:106765844 | TCATTTATATTAGGT[A/T]TATCTCCTAATGCTA | 79589 |
rs187309125 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106733714 | TTTATTTATTTATTT[A/T]TTTTGAGACAGAGTC | 79589 |
rs187507253 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106779189 | ATATTCACTTACTCT[A/G]ATTTTAAATTTATAC | 79589 |
rs187519469 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106764777 | CTAACTTTTAGAATT[A/C]TCTATGCTTTCAAAG | 79589 |
rs187524590 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106745728 | GAAGGAATCAAGAAA[C/T]GCAAATTTGGTTCAT | 79589 |
rs187530575 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106732046 | ACTACATTCAAAGCT[C/T]TATATGTCTCTTCTT | 79589 |
rs187562429 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106747575 | ACCCAATCTTCTGAT[C/T]CCATTTGAGTTACTT | 79589 |
rs187766177 | snp | A/G | 0.00154105 | 0.0277155 | utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106693991 | TAAATTTTATACTCA[A/G]ATGAATGAGCAATGA | 79589 |
rs187784305 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106724568 | ACTTTAGGTTCCAAC[A/C]ATTTTGCATTTACTG | 79589 |
rs187797079 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693600 | TCAGCCTTGTCACGT[A/G]GGATTCCCCAGAGTC | 79589 |
rs187797391 | snp | A/G | 0.016289 | 0.0887646 | intron-variant | RNF128 | GRCh38.p7 | X:106769905 | GTTGTTCCTTTCCAT[A/G]TTTAGTGCTTCCTTC | 79589 |
rs187807265 | snp | A/C | 0.0126344 | 0.0784702 | intron-variant | RNF128 | GRCh38.p7 | X:106709118 | AGAACTTGCCTACTT[A/C]AAGCAAGTTTTATTA | 79589 |
rs187813544 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106753682 | GAATGCATTAAAAAG[A/C]CCCAACTAGCTGCCA | 79589 |
rs187819908 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106738921 | TTTGGAGATTGGCAG[A/T]GTATATCACTGCAGG | 79589 |
rs187827782 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106721950 | ATATAGTAAATGCTC[A/T]ATGAACAGTAGCTGT | 79589 |
rs187891698 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106742089 | TGGTGGCTTGGAGAC[A/C]AGCTAAGGGGTTGTT | 79589 |
rs187943633 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106772334 | CTTAGAACACCTTGA[A/G]CAAATTTTATATTGC | 79589 |
rs187951403 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106705493 | TTAAATCCAATCAAC[A/T]TTTACTTATGTATAT | 79589 |
rs187951496 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106758141 | TAGATGCCAATGGCA[A/C]ACAATCTGAAAAAGA | 79589 |
rs187962181 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106741273 | GTTCTGGATGCTTCA[A/G]TGCTTCTCTTTTATG | 79589 |
rs187972884 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106724223 | AAACCAAGTCCTGTT[G/T]ATTCTACCACCAAAG | 79589 |
rs188027608 | snp | A/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106763877 | TGAGGACTGAAGCAC[A/T]GCATTGTTGCTAAGA | 79589 |
rs188056477 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106709501 | ATATGAAGCTGTGGT[A/G]GTTTTGTGTTGTTTT | 79589 |
rs188058212 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106741947 | GAATCTTATAAAAGG[A/T]GGTTCAATTTTATTC | 79589 |
rs188097023 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106703881 | GATGCTGATAATATA[C/T]AGAGTATGGCCATGG | 79589 |
rs188142239 | snp | A/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106794624 | CAGGATCTGAGCAAC[A/G]GGCATGCTTATTGCT | 79589 |
rs188169951 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106759055 | CAAGGGATTAATAAC[C/G]AGAATACTTAAGGAG | 79589 |
rs188282968 | snp | A/C | | | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106795965 | TTTTTAGACATTCAA[A/C]ACTGTCTTCAAGAAG | 79589 |
rs188302987 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | RNF128 | GRCh38.p7 | X:106778271 | TATTATGCTAACTGT[A/G]TAGTAACTATACTGA | 79589 |
rs188311234 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106701682 | AAGAAATTTCATTGT[A/G]ACTCCGAGTTGAGTG | 79589 |
rs188319477 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106745356 | GATCTGTGATAATCC[A/G]GAATATTAAGAACCA | 79589 |
rs188447263 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106749348 | TTGGAATTCGCTGGC[A/G]CATTATAAGAGACCC | 79589 |
rs188455102 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106736468 | ACACCCCTCTTAGAG[C/T]TTCTTTTTCCTTTTC | 79589 |
rs188463759 | snp | C/G | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106719538 | GGGCACTTTTAATAA[C/G]TTAATTTCTCCCTAA | 79589 |
rs188465075 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106738334 | TTTAGTAAATGCTAG[A/T]TCTCTTGAACCTTTG | 79589 |
rs188554085 | snp | A/G | 0.000167328 | 0.00914527 | intron-variant | RNF128 | GRCh38.p7 | X:106785181 | TTTTAAAGCAGTGCT[A/G]CCAAGCCATTGTTCA | 79589 |
rs188554606 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106786881 | TAATTAAAGAAATAC[A/C]AATTAAAGCCACAAT | 79589 |
rs188556011 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106766716 | AGAAGCTCTTTAGTT[C/T]AATTAGATCCCATTT | 79589 |
rs188564258 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106749938 | ATTAGGTATGCACAA[A/G]TGAAAAGAATAGCAA | 79589 |
rs188572058 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106697591 | CCTCCGCATCCCTTA[C/T]AGGTTGCCTTCAAGG | 79589 |
rs188572079 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106753127 | GGTGGTAGAGAGATC[A/G]AGATAGAAAGCATAT | 79589 |
rs188574674 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106736982 | CATCGAGTATGGATT[A/T]TTATATTATTCCCAA | 79589 |
rs188609516 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106694610 | AGTAGCAATTCATGA[A/G]GTGATTCCTATTTTC | 79589 |
rs188642321 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106715879 | TACTCTTCTCCTCAT[A/G]AAAGAGATTGAATAA | 79589 |
rs188698567 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106746625 | CCCAAGATAGACATT[C/T]TTTGTATTAACATTT | 79589 |
rs188702979 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106733184 | ATATGCACACATTGA[A/G]CCATTTTATATAAGG | 79589 |
rs188703707 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106702824 | GGAAGAGTGAATTCC[A/T]GGAGATGATGTTTCA | 79589 |
rs188714238 | snp | C/T | 0.0105399 | 0.0718252 | intron-variant | RNF128 | GRCh38.p7 | X:106744817 | CTAATGTGGTAAATA[C/T]CAATAGAAATAATCT | 79589 |
rs188761674 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106706926 | TCTTCTTCACCTGTC[C/T]GTGTCTCTTTCCCAC | 79589 |
rs188813239 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106793044 | TCATTGGGCTAAGTT[C/T]TATTAGAGCACTGGT | 79589 |
rs188817248 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106766166 | TTGTGAATAGTGCCG[A/C]AATAAACATACGTGT | 79589 |
rs188819858 | snp | C/T | 0.01368 | 0.0815649 | intron-variant | RNF128 | GRCh38.p7 | X:106713923 | GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG | 79589 |
rs188831850 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106735912 | TTACCCTCCCCCCAA[C/G]ACACACACACATAAA | 79589 |
rs188835711 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106705024 | GTGAATAAATTTAAA[A/T]CACAAGGGTTTGTTC | 79589 |
rs188952234 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106787735 | TATTCTTTTACCTTT[C/T]TAAAGTCTGGATACT | 79589 |
rs188981758 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106763422 | AGAACAGTGGAGGGG[G/T]AGCAGTTTACAGATA | 79589 |
rs188990007 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106718968 | TAATCCTAATGCATA[G/T]AGTTGGCAGCTGTGA | 79589 |
rs188997523 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106695590 | TCCTGGACACTGCAA[G/T]AGCTCAGACATTCAC | 79589 |
rs189003259 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106730111 | CTGAGTGTCTATATT[A/C]CCACCTAACTAATTT | 79589 |
rs189082422 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106784271 | ACCATACATAGAGGG[A/G]CAATGTGTTATTGAA | 79589 |
rs189092091 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106696872 | AGCACACACCATGGA[A/C]AACCACAGGGCATCC | 79589 |
rs189098390 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106748809 | GGGGCACAAAAATAC[A/G]GTTAGACAGAAGAAA | 79589 |
rs189191025 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106781793 | TGCAAATCTTTTAGA[G/T]ATCCTTTATAATCAA | 79589 |
rs189191780 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106790794 | GGCCTAACTTGTACC[C/T]AGCATTATTTTATGA | 79589 |
rs189195473 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106765800 | TTTACATGTGCCATG[C/T]TGGTGTGCTGCACCC | 79589 |
rs189195683 | snp | A/G | 0.00844089 | 0.0644143 | intron-variant | RNF128 | GRCh38.p7 | X:106771455 | AGCCTCAGCAATGGC[A/G]TACGCCCCTCCCCCA | 79589 |
rs189202571 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106754692 | TCCTGAATGACCAGT[A/G]GGTTAATGTAGAAAT | 79589 |
rs189207585 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106747370 | CATCAGATACTTTTA[A/G]CAAATTAAGGACTTT | 79589 |
rs189213359 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106739928 | CTACTGGAACTCTTG[C/T]ACCCTTGGATTTTGT | 79589 |
rs189222567 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106723206 | GATTTATCACTTGTT[A/G]TCATTTTGCCATATT | 79589 |
rs189266115 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106695421 | TGCTTGGAATGTTCC[A/G]AGTTGTACACATACA | 79589 |
rs189275198 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106712440 | TGTTAATGCTTTAAG[C/T]GTATAATTCTTCTAA | 79589 |
rs189289653 | snp | A/G | 0.220783 | 0.248287 | intron-variant | RNF128 | GRCh38.p7 | X:106712904 | TTTTTTTTTGAGATG[A/G]AGTCTCACTCTGCGG | 79589 |
rs189312413 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106760905 | AAAGCAAAAACAAAA[A/G]CAAAAGTTGGCAAAT | 79589 |
rs189316688 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106784729 | AAAATGCATATTAAT[A/G]TCCTCTGAGCTTGCA | 79589 |
rs189332219 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106726466 | CAAAACCGACTCGAA[C/T]CCTGCCAGAAAGCTT | 79589 |
rs189335659 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106794945 | AATAGTTTCAGCATT[A/G]CTAACACATACCCCT | 79589 |
rs189342080 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106773751 | ATAAAAAGGTACAAG[G/T]TACACAAACAACAGA | 79589 |
rs189342162 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106760464 | AGTTAGGATGGCTAT[C/T]ATAAAAGAGACAAAA | 79589 |
rs189355510 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106743219 | TATTTGTTGCCAATG[A/G]TAAGATTTAAGTTTT | 79589 |
rs189363903 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725598 | TAATATTATTTTAGA[A/G]TTGTGTCTCTGAACC | 79589 |
rs189411278 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692290 | ACAGGCTTTATTGTG[A/G]TCCTAAAAACACATC | 79589 |
rs189421902 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106707353 | CAAAATGTGCCTTCC[C/T]CTAACTTTCACACAT | 79589 |
rs189475338 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106719753 | TATTACTATTTTAGT[A/T]GAGAAAGAAGAAACA | 79589 |
rs189510681 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106706101 | ATGATACCTCCACGA[C/G]ATGGGAGACCAAGGG | 79589 |
rs189563709 | snp | A/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106704573 | GAAGGAGAAGTCGTG[A/T]CCTCATGATAAGACG | 79589 |
rs189577742 | snp | G/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106765631 | GAAGATACAACAGAG[G/T]GTGTCTACATTTCAG | 79589 |
rs189590530 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106775149 | TAAAATTCCTGTACC[A/T]GGCCACTCAGTAGTT | 79589 |
rs189607992 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106743341 | ATTAACAACTGACTT[A/T]TTTGTTATTGTTTTA | 79589 |
rs189612418 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106739169 | TTCTTTCTTTCTGAC[A/T]TTTTTTTTGAGACGC | 79589 |
rs189618048 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106766552 | CTTTGCCCACTTTTT[C/G]ATAGGGTTGTTTGAT | 79589 |
rs189689976 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106765965 | TGAGTGAGAACATGC[A/G]GTGTTTGGTTTTCTG | 79589 |
rs189690871 | snp | A/T | 0.000529661 | 0.016265 | downstream-variant-500B | RNF128 | GRCh38.p7 | X:106797055 | GTGTCACTATAAAGG[A/T]ATACCTGAGACTGGG | 79589 |
rs189693507 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106791565 | GAGCCATTGTTTATT[G/T]CAGATAAAGCAGAAA | 79589 |
rs189693661 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106748120 | GTAACCCATTTTTGG[C/T]TTCTTAAGCCTGGTA | 79589 |
rs189695750 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106771711 | ACTTCCTGGGTGAGG[C/T]GATGGCCTGCCCTGC | 79589 |
rs189699881 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106734094 | GCTTTCTATTGTAAG[A/G]ATTTCTCCATGTATC | 79589 |
rs189716369 | snp | A/G | 0.00791544 | 0.0624105 | intron-variant | RNF128 | GRCh38.p7 | X:106717800 | GATTAAGTGGGATTC[A/G]TCTAGCACATTTTTC | 79589 |
rs189821241 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106785989 | CTGTTGTTAAGATGT[C/T]GGTTCCCCACCAAAC | 79589 |
rs189826059 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106768935 | TGTTCTCATTGGTTT[C/T]AAAGAACATCTTTAT | 79589 |
rs189838626 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106751578 | ATATGGCCAAGAAAG[C/T]GTTTGCATCACCCCT | 79589 |
rs189846852 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106737810 | CTTTCATAGGTGTGT[A/T]TCAATCAAATTCTTT | 79589 |
rs189848038 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106781233 | AGAGGTGGAAATAAT[A/G]TGTTACTGGAATTTA | 79589 |
rs189857045 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106720886 | TAGTAGGCTCTCAAT[G/T]GTAGTTATTAAAGTT | 79589 |
rs189896801 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106722595 | GTACTTTGTTGCAGT[C/T]ATGATCTACAATCTG | 79589 |
rs189930830 | snp | A/G | 0.0792336 | 0.182589 | intron-variant | RNF128 | GRCh38.p7 | X:106704202 | GCACTTTGGGGGGCC[A/G]AGAAGGGCAGATCAC | 79589 |
rs189950188 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106769359 | TGTCTAAGTCTCTTT[G/T]TAGGTCTCTAAGGAC | 79589 |
rs189958395 | snp | A/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106752872 | AGATTGAAATACTTT[A/T]AAAAAATCAAGCATA | 79589 |
rs189980996 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106768006 | GGTTCTGTTTATATG[A/C]TGGATTACATTTATT | 79589 |
rs190100676 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106701262 | GATAACAGTATACAT[C/T]CTTGACTTGTTCTTG | 79589 |
rs190118752 | snp | A/G | 0.000297326 | 0.0121891 | missense | RNF128 | GRCh38.p7 | X:106790233 | GGCTGTTAGAACACA[A/G]GACTTGCCCCATGTG | 79589 |
rs190126524 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106728087 | AGGCCTAGACTTTGG[A/G]AAAAAAAATAGTCCA | 79589 |
rs190139533 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106754151 | CTACAGAAGACACAA[C/T]TGTCTCTTTGGCACG | 79589 |
rs190160594 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106723073 | TCATACCATTCATTC[A/G]CTCCATTGACTTCAA | 79589 |
rs190232656 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106785651 | TTGGTTATAGACTTC[A/G]GATTTCCAGAACAGT | 79589 |
rs190273518 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106780555 | TTAGAGAGGAGGAGG[A/G]GAAAGGCAAAAGGCG | 79589 |
rs190285122 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106746208 | TATTATTCTCATTGT[A/G]AATAACCTCTATTTT | 79589 |
rs190344587 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106695903 | TTTCTTTGCAACCTG[C/T]ATTAGGGACCAATAT | 79589 |
rs190351462 | snp | A/G | 0.0792336 | 0.182589 | intron-variant | RNF128 | GRCh38.p7 | X:106704211 | GGGGCCAAGAAGGGC[A/G]GATCACGAGGTCAGG | 79589 |
rs190354740 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106713279 | TTTGGGAAGCCAAGG[C/T]GGGTGGATTGCTTGA | 79589 |
rs190387459 | snp | A/G | 0.0126344 | 0.0784702 | intron-variant | RNF128 | GRCh38.p7 | X:106770623 | TAAGGACTTCTCTAC[A/G]CTGTTTATTCTAGTT | 79589 |
rs190402021 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106739702 | TAAGTGAGACAGATT[C/T]ATGTTTGGTTTTATA | 79589 |
rs190402748 | snp | A/C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106737323 | CTGGTGTGCTGCTAG[A/C/T]TTTTCAAGTACAGTT | 79589 |
rs190470242 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106715449 | TAATCAGTGGATAAT[A/G]TGGTTTTACAAAAGA | 79589 |
rs190488300 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692873 | TGTTTGTCTAGTTTG[C/T]TGACTCTTGGCCCAG | 79589 |
rs190499303 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106708683 | TCCAGCAGTGCTTCT[C/T]TTTGGCATCATTTTA | 79589 |
rs190527083 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106765283 | TCAAATAAAGAGAGA[A/G]TCTTAGCATACTATG | 79589 |
rs190542852 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106732312 | CCTCTCTTATAGTAC[A/G]TTCTGCATTTTGCTG | 79589 |
rs190606767 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106777197 | GACATTGAACTAAAA[A/G]CTCCTCACAGTGTGA | 79589 |
rs190622613 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106762905 | AGGATGAATACCTAT[C/T]GGGCACTATGCTTAT | 79589 |
rs190629947 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106744660 | GAGACGGGGTTTCAC[C/T]GTGTTAACCAGGATG | 79589 |
rs190643683 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106696932 | GGATTTGGGCTTGCT[G/T]ATGTGTTTTGGGGGA | 79589 |
rs190645209 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106751380 | ATACCCATGGAGGGA[A/G]CATTTAGACCAGCCC | 79589 |
rs190660946 | snp | A/G | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106720510 | TGAGCCACCACACCC[A/G]GCCTCATAATCTCTG | 79589 |
rs190708613 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106698403 | CAGAGTAGTGAAGTG[A/C]ATGAAAAGGAAGGGT | 79589 |
rs190766875 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106724003 | AGGTGTTCAGTGATC[A/G]GAAACTCAACTGCCT | 79589 |
rs190781227 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106733425 | AGTACTAAAGACATT[C/T]TCTAAGTAATTTTCT | 79589 |
rs190859479 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106793311 | GCTGATGTTTGGACT[A/G]TACCTCAGAGCAACT | 79589 |
rs190863558 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106772348 | AGCAAATTTTATATT[C/G]CTTTTGAGGATATAG | 79589 |
rs190866058 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106758453 | AATTTATATGAAACC[A/G]CAGAAGACCCAGAAT | 79589 |
rs190879221 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106763475 | CAAAATGCTTAGAAA[C/T]AGGTCTTTTACATGA | 79589 |
rs190880107 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106741456 | GGGGATTATTTGTCA[A/C]CATTAATGCAGCTCT | 79589 |
rs190885950 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106724281 | CATGTCCACTACCTG[C/T]CTATCCAAGCCATCT | 79589 |
rs190899138 | snp | G/T | 0.00422943 | 0.0457911 | intron-variant | RNF128 | GRCh38.p7 | X:106730128 | CACCTAACTAATTTA[G/T]AACAGTTGCTTTAAA | 79589 |
rs190907071 | snp | A/C | 0.0105399 | 0.0718252 | intron-variant | RNF128 | GRCh38.p7 | X:106714332 | TAAAGTTGAATTCAA[A/C]TAATGCATTATACAA | 79589 |
rs190988546 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106783607 | AAAATAGAAAGATCA[C/T]TTATCTTGCCATGCT | 79589 |
rs191026904 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106713729 | GCTACCATATTGAAC[A/G]GTATATGAACATGAA | 79589 |
rs191027400 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106755568 | AGGGTAATTGATCAT[A/G]ATCAAGTGGGATTTA | 79589 |
rs191034278 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106776421 | AAAAGGATTTACTAA[C/T]TAAAATAGACAGATT | 79589 |
rs191037075 | snp | A/C | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106729509 | AAATGTATGATTGTG[A/C]AACTGTCGATTTGAA | 79589 |
rs191046498 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106721301 | TAGATGCCAGGATAC[C/T]GTTTGTCCCAAGTTG | 79589 |
rs191051200 | snp | G/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106744118 | GGTGGGGGAAGGGGG[G/T]AGGGATAGCATTAGG | 79589 |
rs191128849 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106777745 | GAGGCCGAGGCGGGT[A/G]GATCGCTTGAGCCCA | 79589 |
rs191137702 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106744984 | GAATAGTTCAAGCAG[A/G]ATCAGGTGTTTTATA | 79589 |
rs191161942 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106708015 | ATGAATGAATAAATG[A/C]GTGTATGAAAATGAA | 79589 |
rs191186201 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106740689 | TTCCTCCCGTCTCAG[C/T]TTCTCAAAGTGCTGG | 79589 |
rs191279724 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106738043 | AGATCATCATTTGAT[A/G]GTAAGGAAAGCTATT | 79589 |
rs191315199 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106706071 | TACTAGGCCTCTAAC[C/G]TGATGCATTACCACA | 79589 |
rs191347851 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106784733 | TGCATATTAATGTCC[C/T]CTGAGCTTGCAAATA | 79589 |
rs191363152 | snp | C/T | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106766680 | GCCTGTTCACTCTGA[C/T]GGTAGTTTCTTTTGC | 79589 |
rs191366910 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106749377 | CCTTTCCAATATTTT[A/G]AGGATAGAAAAAAGC | 79589 |
rs191373078 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | RNF128 | GRCh38.p7 | X:106794182 | TTATTGTACTATAGG[A/G]TCCTAGACGTTTCTT | 79589 |
rs191377417 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106736495 | TTTCAAAAATTTTGT[G/T]CTTCCTTCTATGTGA | 79589 |
rs191386019 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106719657 | GATATTTATTTTAGA[C/T]ATACTATCTGATTTG | 79589 |
rs191393926 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692679 | AGTAGGGAGAAGAAA[C/G]AGCTTCATTGACCAC | 79589 |
rs191416393 | snp | A/G | 0.0121112 | 0.0768695 | intron-variant | RNF128 | GRCh38.p7 | X:106699930 | CTCCCTTGACCTTAT[A/G]CATATTATTTTCTAT | 79589 |
rs191434346 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106723424 | ATACAAAAATTAGCC[A/G]GGCATGGTGGCACGC | 79589 |
rs191461226 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106703936 | GCAACAAAAATTCCT[A/G]AAGTTAAACCACACT | 79589 |
rs191499341 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106787833 | GGAATTTAGGCTGGT[A/T]AAGTACATGTATGTT | 79589 |
rs191499772 | snp | C/T | 0.00949095 | 0.0682305 | intron-variant | RNF128 | GRCh38.p7 | X:106764063 | CACCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 79589 |
rs191502004 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106769971 | ATCTCTCAGCATTTG[C/T]TTGTCTGTAAAGAAT | 79589 |
rs191511229 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106745585 | AGGGTATGCACTACT[G/T]ATTTTGTCTGGTTCC | 79589 |
rs191519482 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106730861 | ATTAATGATTTGGGG[A/G]TCTCCAATGGGATAC | 79589 |
rs191520124 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106739033 | CCTTTTTGTCTTTCC[A/G]AATACTTAACATCCG | 79589 |
rs191530314 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106722184 | AACAGGGTGAAACTA[C/T]ACTTAAATTAACTTC | 79589 |
rs191541305 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106769770 | AGTTAATATTATTAT[G/T]TGTGAATTTGATCCT | 79589 |
rs191548300 | snp | A/T | 0.221574 | 0.248379 | intron-variant | RNF128 | GRCh38.p7 | X:106704591 | TCATGATAAGACGGG[A/T]TTTGGTTGAGTCAGG | 79589 |
rs191675061 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106716265 | CACTTATCTCTCTGA[C/T]CACTCTTTTGTTTAA | 79589 |
rs191687397 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106792944 | ATTACTAGTTTAAGA[A/G]TCTTGCGTATTAGCC | 79589 |
rs191708833 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106755763 | GAGAAGGAAATAAAG[C/G]GTATTCAATTAGGAA | 79589 |
rs191795411 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106787002 | CATTCATTTGCTGGT[G/T]AGAATGCAAAATGTA | 79589 |
rs191825135 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106782874 | CATCAGTTTTCTTCT[A/C]TGTCTGATTAGATGT | 79589 |
rs191832011 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106697259 | TACCCTTATTAGCCA[G/T]AATAGAGAAATATTT | 79589 |
rs191837865 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106714542 | GTTGATACAATCCAC[C/T]CACCTTACTCGAATT | 79589 |
rs191846023 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106747625 | CTCTCTCCCAAACTG[C/T]AGACTGTTTCAGGTT | 79589 |
rs191972577 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106694937 | GATACAAACGAATCT[G/T]CAAAAACGTGATATT | 79589 |
rs191985210 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106710699 | GAGGCAGAGGTTGCA[A/G]TGAGCCAAGGTGGTG | 79589 |
rs191991585 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106771889 | CTCTAAAAGTCCTTT[C/T]AGAGTTGCATGTGTG | 79589 |
rs192002917 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106740849 | TTTTTTAAACTGCCC[A/G]ACAAATAATCTAATT | 79589 |
rs192022367 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106780355 | CAACCCCAATATATT[C/T]CCATTCAGAATCAAG | 79589 |
rs192031270 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106764834 | GAATGCTACATTATA[C/T]AATTAATCACAACTT | 79589 |
rs192042765 | snp | C/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106745870 | AAAATCACTACTTAG[C/G]ATTCTTGGTCTGATG | 79589 |
rs192055666 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106732087 | CCCTAAACATTCTCT[A/G]TTCTTTTCCACTAAC | 79589 |
rs192061590 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106717319 | ATGAAGGATGATTTG[A/G]AATAGGGAAGAGACT | 79589 |
rs192139605 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106765906 | CCAGTGTGTGATGTT[C/G]CCCACCCTGTGTCCA | 79589 |
rs192153980 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106733765 | GAGTACCATGGCGTG[A/G]TCTCAGCTCACTGAA | 79589 |
rs192159802 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106705154 | ATATAAAACTAACCC[A/G]CCCTAGGTTTCCAAA | 79589 |
rs192185485 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106783969 | AAATACCTCCCACCA[C/T]GCCCCACCTCCAACA | 79589 |
rs192185535 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106742268 | TTTTTCTCTGCATGG[C/T]AAAGGATTGGCATTG | 79589 |
rs192188239 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106766162 | GCTATTGTGAATAGT[G/T]CCGAAATAAACATAC | 79589 |
rs192192439 | snp | A/G | 0.00422943 | 0.0457911 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106725119 | CACCAGCAAAATCAG[A/G]CAATTTCTGGAATTG | 79589 |
rs192196926 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106748599 | TACAGCCTTAAAAAA[C/T]GAAATCCTGTCATTT | 79589 |
rs192265992 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106772648 | TGTTGAATTATAGAT[A/G]GTTAATCTGAGGAGG | 79589 |
rs192272831 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106696796 | TCTCCAGCCAAAGAC[C/T]GCTAGCAACAGACCT | 79589 |
rs192279390 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106741963 | GGTTCAATTTTATTC[A/C]GTAGGTGAAATGGAG | 79589 |
rs192339069 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106709672 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 79589 |
rs192385985 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106765411 | CATTTAAGGTTTATA[C/T]CCTTAATTTGAAAAT | 79589 |
rs192414694 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106700672 | CACCCCCAATTCCAG[A/C]ACCTTTTCAAGAGAT | 79589 |
rs192535639 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106753942 | CTGGAGCACCCAGGT[G/T]TATAAAGCAAATATT | 79589 |
rs192539826 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106778903 | TACTCCACTAGTACA[C/T]GAAATTATCTGGAAG | 79589 |
rs192548452 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | RNF128 | GRCh38.p7 | X:106722700 | CTTAACCAAATTCAC[A/G]AGAGACCAATATATA | 79589 |
rs192624229 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106709201 | TTTCCTTTATTTTGT[A/G]TGCTCAGGCTGTACT | 79589 |
rs192641569 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | RNF128 | GRCh38.p7 | X:106703469 | ATGGTCATACAGCTA[C/G]TACGTTTCAAAGCTG | 79589 |
rs192678771 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106758937 | AACATGAAGAAAGGA[A/G]ATCACATCAAGCTAA | 79589 |
rs192700683 | snp | A/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106724667 | CTGCCTAGAAAAGTT[A/T]ACTGTCTCAAACTCA | 79589 |
rs192740854 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106780570 | GGAAAGGCAAAAGGC[A/G]TTTGACATCATATAC | 79589 |
rs192752988 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106746365 | ATTGTAAAAATATTT[C/T]AGAATTTATTTTACA | 79589 |
rs192823629 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106739200 | AGTCTTGCTCTGTCA[A/C]CCAGGCTGGAGTGCA | 79589 |
rs192892199 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | RNF128 | GRCh38.p7 | X:106738414 | AGATATTTACTACCA[C/T]ACTTTGAAATATGTA | 79589 |
rs192918385 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106715228 | ACACATTATTTTTTT[A/T]AATTTTAGCCATTCT | 79589 |
rs192928857 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106794749 | CTCTATCTGTCATTT[C/T]ATCTATCTATCTGAA | 79589 |
rs192942059 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106759593 | ACACACAATGGAGTA[C/T]TATTCAGCCATAAAG | 79589 |
rs192956648 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106734294 | TGAAATATACTTACT[A/G]GCCTTAAACATGGTC | 79589 |
rs192994965 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106706419 | AACAAGGGTTTACTT[A/C]TTCACTCAACAAATG | 79589 |
rs193003577 | snp | C/G | 0 | 0 | intron-variant | RNF128 | GRCh38.p7 | X:106784345 | CTTCCCACACCCCAA[C/G]TTCACTTCTGACTCA | 79589 |
rs193009844 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106770452 | TTCATTTCTTTTTAC[A/T]CTTTTTTTTCCTCTA | 79589 |
rs193011806 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106749179 | CACTTTCTATTCCCT[A/G]ACACACTGAAAATCG | 79589 |
rs193051134 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106718789 | AACATAACCGTAACA[C/G]TTGTCTAATTCTGGT | 79589 |
rs193098876 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106753311 | TAAAAAGCCATGGAG[G/T]GGATAAAGTTAAAGT | 79589 |
rs193133426 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693829 | GGGAATGTAGATAAC[C/T]AAAGTGAAATAGAGC | 79589 |
rs193141321 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106719107 | ACTACAGTAGAAGGA[C/T]GTTTATTCATAAATT | 79589 |
rs193144253 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106721465 | AATGGTTCCCTGCTG[A/T]TGCTCCTGCAGAATG | 79589 |
rs193159541 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106697670 | TTCATGATTTAAATA[A/C]AGAATGTCCTTACTC | 79589 |
rs193170952 | snp | C/G | 0.00168265 | 0.0289568 | intron-variant | RNF128 | GRCh38.p7 | X:106773171 | AGCAGGTTTGTAATG[C/G]TCCTTTCTTCCACTA | 79589 |
rs193206349 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106766178 | CCGAAATAAACATAC[A/G]TGTGCATGTGTCTTT | 79589 |
rs193211320 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106736167 | GTATTAGATTAAGGG[A/C]AGAAGGGAATCGTGA | 79589 |
rs199646117 | in-del | -/TTTG | 0.0575773 | 0.159604 | intron-variant | RNF128 | GRCh38.p7 | X:106753350 | TCAATTAGTTTTCTC[-/TTTG]TTTGTTTGTTTGTTT | 79589 |
rs199720554 | snp | A/G | 4.82946e-05 | 0.00491375 | missense | RNF128 | GRCh38.p7 | X:106694372 | ATTTACAATGCTCCA[A/G]AGACTGGCAATCAGA | 79589 |
rs199736838 | in-del | -/TAT | 0.0256233 | 0.11025 | intron-variant | RNF128 | GRCh38.p7 | X:106789562 | ATATATACTATATAA[-/TAT]TATAATATGTAGTAT | 79589 |
rs199745885 | in-del | -/A | | | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106693676 | TGGAACAGTAAGAAG[-/A]AAAAAAAAATGTACT | 79589 |
rs199754461 | in-del | -/CTAA | 0.0379276 | 0.132383 | intron-variant | RNF128 | GRCh38.p7 | X:106707125 | ATAATTCCTGAATTC[-/CTAA]CTATTATAGACTAAT | 79589 |
rs199783062 | in-del | -/T | 0.0570788 | 0.159001 | intron-variant | RNF128 | GRCh38.p7 | X:106772146 | AATGTTTGTACTTTA[-/T]TTTTTTCCACAAAAC | 79589 |
rs199917981 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106744681 | AACCAGGATGGTCTC[C/T]ATCTCCTGACCTCGT | 79589 |
rs199985025 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106769941 | CTCTTGTAAGGCAGG[C/T]CTGGTGGTGACAAAA | 79589 |
rs200002371 | in-del | -/TATT | 0.103655 | 0.20269 | intron-variant | RNF128 | GRCh38.p7 | X:106789435 | ATAATATATAGTATA[-/TATT]ATATACATTATACAC | 79589 |
rs200207463 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106789598 | TAGTTACACATGTAA[A/C]TATAAGGACAGTACT | 79589 |
rs200236070 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106788366 | TATATACTATATATA[A/T]TATATATTATATATT | 79589 |
rs200303514 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106704588 | TCCTCATGATAAGAC[-/G]GGTTTTGGTTGAGTC | 79589 |
rs200492021 | in-del | -/A | 0.22669 | 0.248911 | intron-variant | RNF128 | GRCh38.p7 | X:106700546 | TTTGGTAAATTTGGC[-/A]AAACTATTGTATTTT | 79589 |
rs200502824 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106715156 | TTTCACATTCCCACC[-/A]AAAAAAAATGTACGT | 79589 |
rs200521848 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106763722 | CGTGTTAGCCAGGAT[G/T]GTCTCGATCTCCTGA | 79589 |
rs200538139 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106765813 | TGTTGGTGTGCTGCA[C/T]CCATTAACTAACTCG | 79589 |
rs200607948 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106753701 | ACTAGCTGCCATCCT[-/G]TAAGAAACACACTTC | 79589 |
rs200615106 | snp | C/T | 5.41675e-05 | 0.00520392 | utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106693963 | TGATAGTTGGAAATA[C/T]CAGCAAACATCTTAA | 79589 |
rs200654788 | in-del | -/A | 0.100346 | 0.200259 | intron-variant | RNF128 | GRCh38.p7 | X:106779607 | AATCACATTTCTTTG[-/A]AAAAAAATGCTGTAA | 79589 |
rs200696798 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106769384 | AAGGACTTGCTTTAT[A/G]AATCTGGGTGCTCCT | 79589 |
rs200766025 | snp | C/T | 4.68565e-05 | 0.00484005 | intron-variant, synonymous-codon | RNF128 | GRCh38.p7 | X:106727267 | AGTCTCTTGGTTGGC[C/T]CTCATCCAACGCGGC | 79589 |
rs200832746 | snp | C/T | 4.90004e-05 | 0.00494952 | intron-variant, missense | RNF128 | GRCh38.p7 | X:106727221 | CGCACACGAATTTCA[C/T]GGTGCCCACGGTTTG | 79589 |
rs200834362 | snp | A/G | 0.000114163 | 0.00755437 | missense | RNF128 | GRCh38.p7 | X:106694194 | AGTGGCTAATGCTAT[A/G]GGAGTGGTAGGCATC | 79589 |
rs200846586 | in-del | -/T | 0.01368 | 0.0815649 | intron-variant | RNF128 | GRCh38.p7 | X:106711698 | GTTTATTTTTCCATA[-/T]TTTTTAAATTTTATT | 79589 |
rs200872310 | snp | A/T | 0.00048083 | 0.0154979 | missense | RNF128 | GRCh38.p7 | X:106795685 | AAACTCCTAATCAAG[A/T]GACTGCTGTTCGAGA | 79589 |
rs200927986 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106769950 | GGCAGGCCTGGTGGT[A/G]ACAAAATCTCTCAGC | 79589 |
rs201049142 | in-del | -/T | 0.0168099 | 0.0901243 | intron-variant | RNF128 | GRCh38.p7 | X:106735962 | TTCTTTGTATTTTTG[-/T]TTTTTTTTTCCCGTA | 79589 |
rs201052407 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106791916 | TCCATGTTTTTGTTG[A/G]TTTGAAAGTCTTCTC | 79589 |
rs201232941 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106786264 | GAGTACAGAAATAAA[A/C]CCATATATATATGGT | 79589 |
rs201266503 | snp | A/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106743912 | TATACACCATGGAAT[A/C]CTATGCAGCCATAAA | 79589 |
rs201268269 | snp | C/T | 2.29116e-05 | 0.00338456 | synonymous-codon | RNF128 | GRCh38.p7 | X:106772941 | TGTTGCAATCATGAT[C/T]GGCAATCTGAAAGGC | 79589 |
rs201369250 | in-del | -/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106718315 | TCAATTTCTGCCCTC[-/T]TTTTCCCCCTCTCGA | 79589 |
rs201396489 | in-del | -/AAAAAAAAC | 0.0173306 | 0.0914601 | intron-variant | RNF128 | GRCh38.p7 | X:106706388 | TGCTTCCTTATGTGA[-/AAAAAAAAC]AAAAAAAAACAAGGG | 79589 |
rs201396943 | snp | C/T | 0.000151139 | 0.00869176 | synonymous-codon | RNF128 | GRCh38.p7 | X:106694407 | ACAGATGGCAAATTT[C/T]GGTAAGTAATAATTG | 79589 |
rs201435320 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106757111 | GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA | 79589 |
rs201450303 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106712620 | TACACATCTAAAATG[C/T]TACTCAACTCAGCTA | 79589 |
rs201498826 | in-del | -/C | 0.00633741 | 0.0559334 | intron-variant | RNF128 | GRCh38.p7 | X:106782849 | AAGCAAGACATTCTT[-/C]CTCTTTGAGCATCAG | 79589 |
rs201505875 | in-del | -/TA | | | intron-variant | RNF128 | GRCh38.p7 | X:106789453 | ATATACATTATACAC[-/TA]TATATAATATAGTGT | 79589 |
rs201552916 | in-del | -/T | 0.0266548 | 0.112325 | upstream-variant-2KB | RNF128 | GRCh38.p7 | X:106692716 | CAACAACGTCTCCTA[-/T]TTTTTTATTTTCGGT | 79589 |
rs201622989 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106727438 | CCTCCAGACCTCTGC[C/T]ATGGCCAGTTTCTCT | 79589 |
rs201767153 | in-del | -/C | | | intron-variant | RNF128 | GRCh38.p7 | X:106769705 | AGTCTGTGTCTTTTT[-/C]TTTTCAGTCTATGTC | 79589 |
rs201787785 | snp | A/G | 2.33078e-05 | 0.0034137 | intron-variant | RNF128 | GRCh38.p7 | X:106790159 | TGCTACTTTACAACT[A/G]ATAATTATGTTTTTT | 79589 |
rs201809468 | in-del | -/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106700547 | TTGGTAAATTTGGCA[-/G]AACTATTGTATTTTT | 79589 |
rs201834617 | in-del | -/A | 0.0369084 | 0.130736 | intron-variant | RNF128 | GRCh38.p7 | X:106757749 | TAAAAAAATAAATTT[-/A]AAAAAAACCCTAAAA | 79589 |
rs201851016 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106769952 | CAGGCCTGGTGGTGA[C/G]AAAATCTCTCAGCAT | 79589 |
rs201876772 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | RNF128 | GRCh38.p7 | X:106788328 | TATGTATTAATATTA[C/T]ATATACTATATATAA | 79589 |
rs201880810 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | RNF128 | GRCh38.p7 | X:106769598 | ATATCTTCCTCCATC[A/C]CTTTATTTTGAGCCT | 79589 |
rs202026628 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106757613 | GGGGGAGGGATAGCA[C/T]TGGGAGATATACCTA | 79589 |
rs202169651 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106744629 | CATGCCCAGCTAATT[A/T]CTTGTATTTTTAGTA | 79589 |
rs367545574 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106722745 | TTGATTAATTTATAA[A/T]GAGAAGTACAACTTC | 79589 |
rs367570137 | snp | A/C | | | intron-variant, utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106726783 | GCCTCCTGGCTCCGA[A/C]GTAGCTCGCAGCTCC | 79589 |
rs367592609 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106704082 | GCAGAGAGGAAGGTA[A/G]TAGAGGTTATTAAAA | 79589 |
rs367594485 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106793389 | TAATTTGAAATGATT[A/T]CAGACTGACTGACAA | 79589 |
rs367606456 | snp | G/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106769864 | GGTCTTTACAATTTC[G/T]CATGCTTTTGCAGTG | 79589 |
rs367623563 | snp | A/G | 2.56558e-05 | 0.00358152 | synonymous-codon | RNF128 | GRCh38.p7 | X:106787995 | GGTACGCATCTTAAC[A/G]TGCAAGTAAGTTTGA | 79589 |
rs367708254 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106783423 | ATTTTATTGAGTATC[C/T]GCTATATGCCAGACA | 79589 |
rs367774801 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106782520 | TGTATTGTAATGGAC[A/T]CTTGGAATATGAAGA | 79589 |
rs367778004 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106738740 | ACCTTAACCAAATTA[A/G]TCTAAGACTCAGTTT | 79589 |
rs367893708 | in-del | -/AATA | | | intron-variant | RNF128 | GRCh38.p7 | X:106741031 | TAGAAAACATAAATA[-/AATA]GCAACTGCAAATGTT | 79589 |
rs367937431 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106751475 | GTCCTAAATAAATAC[A/G]AAAGGCAGTCTAGAC | 79589 |
rs367949961 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | RNF128 | GRCh38.p7 | X:106724529 | TACCTCTCCAACATG[A/G]TCTGTTACCACCCTC | 79589 |
rs367954696 | snp | A/G | 0.00808497 | 0.0630644 | intron-variant, utr-variant-5-prime | RNF128 | GRCh38.p7 | X:106726902 | GCTAGGGAACTGCGG[A/G]GCGCGCGCGCCATGG | 79589 |
rs367954985 | snp | A/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106730022 | TTCTGTATCTTCTTT[A/G]TTTACAAAATCTCTC | 79589 |
rs367990054 | snp | C/T | | | utr-variant-3-prime | RNF128 | GRCh38.p7 | X:106796221 | GCTGCTTTAAGTTAA[C/T]AGAAAAGATTAAAGC | 79589 |
rs368005586 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | RNF128 | GRCh38.p7 | X:106781362 | AGTAAGGTACAAATT[A/G]CAGTTCACATGGGGC | 79589 |
rs368045213 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106697923 | CTATCTATCTACACA[C/T]AAACATATATGTATA | 79589 |
rs368126599 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106700621 | TTCTCCTATAAAAAA[-/A]CACTAACAATATAAC | 79589 |
rs368142694 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | RNF128 | GRCh38.p7 | X:106784462 | TGAAACAATAAAAGG[C/T]GACCACTCTCAGAAT | 79589 |
rs368147121 | snp | C/G | 2.28741e-05 | 0.0033818 | missense | RNF128 | GRCh38.p7 | X:106790236 | TGTTAGAACACAGGA[C/G]TTGCCCCATGTGCAA | 79589 |
rs368178339 | snp | C/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106765882 | CAGCCCCCCACCCCA[C/T]GACAGGCTCCAGTGT | 79589 |
rs368234138 | snp | A/G | 0.000135717 | 0.00823652 | intron-variant, synonymous-codon | RNF128 | GRCh38.p7 | X:106727117 | GGAGCTGAGCGAGGA[A/G]GGCGTGTACGGCCAG | 79589 |
rs368285122 | in-del | -/A | | | intron-variant | RNF128 | GRCh38.p7 | X:106754958 | ATTGAAATAAAAAAA[-/A]CACAAAACATCAATG | 79589 |
rs368312753 | snp | A/T | | | intron-variant | RNF128 | GRCh38.p7 | X:106770005 | ATTTCTCCTTCACTT[A/T]TGAAGCTTAGTTTGG | 79589 |
rs368330115 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106753213 | GAGTAGGAAGACTAA[C/G]AGATGAACCTATCAA | 79589 |
rs368337985 | snp | C/G | | | intron-variant | RNF128 | GRCh38.p7 | X:106702748 | CCTAGAAACAACATG[C/G]CTTAAAAGAAAAACA | 79589 |
rs368382668 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | RNF128 | GRCh38.p7 | X:106702542 | CAGTCCTCAGTTCAT[A/G]AGTGCTCTTACCCCA | 79589 |