SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs14137 | snp | C/T | 0.494007 | 0.0544111 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620492 | AGTACTTGGTGATGA[C/T]GCCAGATAGGGAACT | 51133 |
rs908480 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590774 | TGTTAAAGTATTTGT[C/T]TGCTAATATCAATAT | 51133 |
rs1074255 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590080 | caaagtgttgattag[C/G]atgtggagaacctgg | 51133 |
rs1342802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606876 | ATTAGCAAAATTGAC[A/G]TAATTGTCCAATTGA | 51133 |
rs1819739 | snp | C/G | 0.43309 | 0.17023 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591054 | AAAATAAGAACTACA[C/G]CCTTGAAAAGGAGCC | 51133 |
rs1819740 | snp | A/G | 0.109108 | 0.206518 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590903 | gttatgaattatgtt[A/G]cctttctttaaaagt | 51133 |
rs2185824 | snp | A/T | 0 | 0 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620908 | ATATTACCACGTCTT[A/T]ATAGGATGGTGCCCA | 51133 |
rs2275768 | snp | G/T | 0.426234 | 0.177318 | missense, utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567710 | GGGCACTGCGGCAGC[G/T]TCCCCGCGGCGGCGG | 51133 |
rs2459573 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582495 | TAAGATGATGGAGAG[A/G]TGAAATAACAGAGCA | 51133 |
rs2675222 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570343 | ATGAAACTTCATCTA[C/T]TCTACTTTCTGAATC | 51133 |
rs2675223 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597033 | ATACTGCAGAGATTA[A/T]TCGTACATTTGCAGT | 51133 |
rs2675225 | snp | G/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618511 | GTCAAGTACAATTCA[G/T]TTAGCCCTTACGTGA | 51133 |
rs2675226 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613464 | TGTCTGTTTACTCTG[A/T]TGATAGTTTCTTTTG | 51133 |
rs2677115 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579622 | tcctgcctcagcctc[C/T]ggagtagctgggact | 51133 |
rs2677117 | snp | A/G | 0.492533 | 0.0606443 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617663 | acatgcagcaagcca[A/G]aagattttctcggag | 51133 |
rs2797253 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610887 | CATAGTAAGTACAGT[A/G]TAAGTATTAGCTAAT | 51133 |
rs2797391 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571606 | AAATTGTAAAGTTGT[A/G]TGTGGGAAGAAGTGG | 51133 |
rs2797392 | snp | A/G | 0.138546 | 0.223781 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597498 | ACAGCTTTGGAAGTT[A/G]GCTCTAGAAAGGCAT | 51133 |
rs2797393 | snp | A/G | 0.494855 | 0.0504572 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600483 | AGCACTGAGATGGCA[A/G]TTCTTCCCCTCTCTC | 51133 |
rs2797394 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603443 | TGCAATGGGGTCTGG[A/G]CACTTTTTGAAAAAA | 51133 |
rs2886165 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614869 | GAATTTTTTACATCA[A/G]AGTTCATTATCAAAT | 51133 |
rs2995519 | snp | A/C | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605584 | atccaaagagttcca[A/C]accctgtatatccag | 51133 |
rs3753836 | snp | G/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600120 | ATACCAGGAAAACAT[G/T]GAGTACTTTTCAGTG | 51133 |
rs3753837 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581758 | CAAATATGTCCTCAA[C/T]TGTCTTCCTTCGTCA | 51133 |
rs3753838 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581589 | CGTAATAATGTGGTG[A/G]TTCTGGAAAAGAGCA | 51133 |
rs3767251 | snp | A/C | 0.0475351 | 0.146656 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621466 | CTACAAGTGAACAAA[A/C]TAGTGTTTTAATTTA | 51133 |
rs3767252 | snp | C/T | 0.0475351 | 0.146656 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621072 | TATCTGGTAAACACT[C/T]TGCAATCACAATAAG | 51133 |
rs3767253 | snp | A/G | 0.0245613 | 0.108062 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620513 | TGAGTCAGTTCCTCC[A/G]TCGGAAGTACTTGGT | 51133 |
rs3767255 | snp | C/T | 0.422158 | 0.181278 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608232 | GGTTTTATTAGTTGA[C/T]ATGCTTCTTCTGAAC | 51133 |
rs3767256 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602663 | TTTTATTGCAATGGC[C/G]TCTAAAATGCACTGA | 51133 |
rs3767258 | snp | A/G | 0.109461 | 0.206758 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600472 | AGAACTGCCATCTCA[A/G]TGCTGGTGGGTGAAG | 51133 |
rs3767259 | snp | A/T | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593210 | AGTGGCAGGTTCATT[A/T]CTTAACCAATTCTGG | 51133 |
rs3767260 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585879 | CTGAAGACTAGTTTT[C/T]AAAGGTCTAAATGCA | 51133 |
rs3767261 | snp | A/C/G | 0.00032241 | 0.012693 | missense | KCTD3 | GRCh38.p7 | 1:215579011 | TGTTGTTTATTTTAC[A/C/G]ACTAGGAATACCTAT | 51133 |
rs3767262 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574261 | TTATAAAAAACTACA[C/T]ATGACAAGAAATAAA | 51133 |
rs4655409 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578590 | GCAAGATTTCATTTT[A/G]AAAAATGTTCCCCTG | 51133 |
rs4655410 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616647 | cgcctgtaatcccag[A/C]tactcaggaggctga | 51133 |
rs4655411 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616648 | gcctgtaatcccagc[C/T]actcaggaggctgag | 51133 |
rs6669126 | snp | C/T | 0.0138664 | 0.082103 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577770 | TTATGATTTGACTCA[C/T]GTATGAAAGTTGCCC | 51133 |
rs6669520 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578352 | gtgtatactacatga[A/C]gactaggtttaactg | 51133 |
rs6674311 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577028 | TTATTAGTATTATAA[A/G]TTCTGAATCTTCCAT | 51133 |
rs6682584 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587626 | tgaactgtgatatct[A/C]tttctgcattcaatc | 51133 |
rs6685149 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587623 | TTTtgaactgtgata[G/T]ctatttctgcattca | 51133 |
rs6685448 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601087 | ggattactggcatgc[A/G]ccactacgcccagct | 51133 |
rs7511859 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574805 | TCTCATTGATTGTAT[A/G]TATATAGTTGATCAT | 51133 |
rs7512596 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569615 | ttttttttttttttg[A/T]gacagagtctcgctc | 51133 |
rs7522198 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574846 | GTTTTATTACTGGCT[A/G]CCATTTCCCTTTCTA | 51133 |
rs7522720 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593490 | TTGTCACTGGTCTTG[A/T]GTATAGTACAGTTCT | 51133 |
rs7528121 | snp | C/G | 0.415563 | 0.18732 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588969 | caaggctttattagt[C/G]tctcagcaattgggt | 51133 |
rs7545425 | snp | A/C | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574892 | CTTTAAAAGATGTTC[A/C]GTTTTTATGGCCAGA | 51133 |
rs10218729 | snp | A/G | 0.00177561 | 0.0297431 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602240 | CATTCTTGACTTTTT[A/G]TCTTTTTATTCATTA | 51133 |
rs10495002 | snp | C/T | 0.100231 | 0.200173 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574581 | TCAGTGCAAAAAAAT[C/T]GGTTTATCCATTTGG | 51133 |
rs10591999 | in-del | -/TC | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591267 | TTTCTTTCTTTTCTT[-/TC]TCTCTCTCTCCTTCC | 51133 |
rs10592000 | in-del | -/TTCC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591288 | TCTCTCCTTCCTTCT[-/TTCC]TTCCTTCCTTCCTTC | 51133 |
rs10612474 | in-del | -/ACT | 0.0599851 | 0.162463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608444 | CTTCACATGTTAACT[-/ACT]TTTATTTATTATTAA | 51133 |
rs11362703 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593878 | GAATTGGAATACAAC[-/T]TTTTTTTTTTTTTTT | 51133 |
rs11558947 | snp | A/T | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621382 | AGACAGGTTAGCAAC[A/T]GGTACAGCTTTCCCT | 51133 |
rs11558948 | snp | A/G | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620741 | GTAATTCTGTTAAAA[A/G]GATACTAAATGAAGT | 51133 |
rs11581370 | snp | G/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593380 | TTCTAACAATACTTA[G/T]CAGGTTTTTTGTTTT | 51133 |
rs11581745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570944 | TCATGAAGTTATATT[C/T]GAGACTGGTTTTGGG | 51133 |
rs11582279 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571920 | acaggcgtgagccac[C/T]gcgcctagccGAGAT | 51133 |
rs11803705 | snp | G/T | 0.420558 | 0.182784 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580012 | CAGGTAGTGTATAAT[G/T]AATAATGCTTTGCTT | 51133 |
rs11805855 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575107 | aaacagaaaaattaa[C/G]ccggcatagtggcag | 51133 |
rs12023213 | snp | C/G | 0.0130921 | 0.0798413 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622195 | CAAGTCAAATCGTTT[C/G]TTTCTTTTGCTTACA | 51133 |
rs12039938 | snp | C/G | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579317 | ATGTTGTGTAATCTT[C/G]TATCTTCTCTGAATC | 51133 |
rs12058673 | snp | A/T | 0.228253 | 0.249052 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566237 | CCAAATTTCCTTTTT[A/T]AAAAATAATTATAAC | 51133 |
rs12070117 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592409 | aagtggagaataatc[A/G]ggtgccatttattct | 51133 |
rs12071678 | snp | C/T | 0.0227044 | 0.1041 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565427 | ATGCCTCAGATATCT[C/T]TATATTGTTCTGGAC | 51133 |
rs12080379 | snp | C/T | 0.195526 | 0.243993 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592206 | GGGCACAGAACCAAA[C/T]TGTATCACTTAGGTC | 51133 |
rs12090919 | snp | C/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589367 | ccaggtcttgaattc[C/T]taagctttagtgatc | 51133 |
rs12124193 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569891 | CATTAAAAAACTTCA[A/G]AAAATTGTTAAGATA | 51133 |
rs12129661 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588451 | tctttgatttggcct[C/T]ttatgttcttgaaag | 51133 |
rs12568192 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617854 | atatttagtatatac[A/G]taatatatattaaat | 51133 |
rs12733007 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589124 | ttaaaatacttaatt[C/T]tttttcttcttttct | 51133 |
rs12741107 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614019 | ggaactttagaatag[G/T]ttttttttttttttt | 51133 |
rs12743895 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602490 | CAAAAAAAAAAAAAA[A/T]TCTGCACATTTGTCT | 51133 |
rs17024959 | snp | C/T | 0.116488 | 0.211364 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607502 | AAAATAATGCTCAGC[C/T]TTAGTACAGAATCTT | 51133 |
rs17024966 | snp | A/G | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608633 | ATATTCTCTGATTTC[A/G]GCAAAAGGTGTATAA | 51133 |
rs17553500 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607245 | GTTCATTGCTAATAA[C/T]AACATATTTTCTAAA | 51133 |
rs28576514 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603009 | GCTCTTTTTGATACC[A/C]CTGTCTTTGGATGTT | 51133 |
rs33997368 | in-del | -/G | | | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620503 | TGGCATCATCACCAA[-/G]TACTTCCGATGGAGG | 51133 |
rs34006906 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579527 | TTTTGAGACGGAGTC[-/C]TCGCTCTGTCGCTCA | 51133 |
rs34019406 | in-del | -/C | | | frameshift-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577710 | ATGAAGCAGAATTTT[-/C]ACGGGATCACTCCAT | 51133 |
rs34191564 | in-del | -/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565965 | AGTGTATTTTATGTG[-/T]GGCCAAAGACAATTC | 51133 |
rs34318346 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587049 | AGACCAGACATTCCC[-/C]AAACTTTTTGGTTTC | 51133 |
rs34340618 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590523 | GGGTTGTGGGAGCCC[-/C]TGATTTTTTATTTCA | 51133 |
rs34352533 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600504 | CCCCTCTCTCCTGTG[A/G]TTGTATTGTAGTCTA | 51133 |
rs34444725 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618566 | TATCCCATTGTTTCC[-/C]TGATCCGTCAATGTG | 51133 |
rs34449729 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597260 | AAATGTTTCAGTTTC[-/C]TTGTTTCCTTTTTTT | 51133 |
rs34486061 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215579305 | TTTTATTTAAAATGT[-/G]TGTGTAATCTTCTAT | 51133 |
rs34694239 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575071 | GCATGGCCAACATGG[-/G]TGAAACCCCCTCTCT | 51133 |
rs34765174 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588656 | ACTATTTCAGCACTT[-/T]CCTGTGTTTGTAGCT | 51133 |
rs34889977 | in-del | -/G | | | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620518 | GTACTTCCGATGGAG[-/G]AACTGACTCACCTGG | 51133 |
rs34983781 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215609907 | AAGAACTTAACTAGA[-/C]AGTTATGTTTATGAG | 51133 |
rs35036763 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597423 | CCCAAGTTGATATTT[-/T]AAATTTAGATTTATA | 51133 |
rs35074372 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569946 | TGGTATGGCCCGTAG[-/T]AAAACAACATCCGAC | 51133 |
rs35128670 | in-del | -/G | | | frameshift-variant | KCTD3 | GRCh38.p7 | 1:215620277 | AAGGGGCAACAGGGG[-/G]AATGTAATATATCTG | 51133 |
rs35231115 | snp | A/C/T | 0.000230713 | 0.0107381 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604217 | AAGCTGAGGACCTGA[A/C/T]CCAACTGTCTCTGGG | 51133 |
rs35331520 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606619 | TAATGTTATTGTGGG[-/C]ATGTGATACCAAGGA | 51133 |
rs35450006 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616548 | GGCGGATCACCTGAG[-/G]TCGGGAGTTCAAGAT | 51133 |
rs35452428 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601634 | GTACTGCTGTGGGAA[-/C]ATACAATTTAAAAAA | 51133 |
rs35511609 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582899 | TTACTTGTATGGAAA[-/A]GTTATAGAGCAAATA | 51133 |
rs35600306 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595208 | AGAGCTTGTGAGTTT[-/T]CTTATTTCTAGTCCC | 51133 |
rs35831873 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596207 | TGACAATCCAGTAGC[-/C]TAGTAGTATTTTGAA | 51133 |
rs36018872 | in-del | -/C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587133 | TTTTCTTTTTTTTCC[-/C/T]TTTTTTTTTTTTTTG | 51133 |
rs36050350 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590141 | TGTGGATTTTAATGG[-/G]TTCAGTGATTTTAAT | 51133 |
rs36095180 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612923 | TTAAACAAATTTTTT[-/T]GACGATGAGAACACA | 51133 |
rs41303271 | snp | C/T | 0.0174825 | 0.0918456 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578972 | AGGTGAACTTAGGAA[C/T]GTATTTGTTTTCTTC | 51133 |
rs55684041 | snp | G/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565481 | GTCTTATAAAATACT[G/T]AGAACTTTTCCTTCT | 51133 |
rs55753515 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578949 | ATGTGATATTTTTAA[A/T]TTTTGAAAGGTGAAC | 51133 |
rs56253877 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594974 | GCATATAACTCACCT[A/G]TGGATTTTGTAACAA | 51133 |
rs56770054 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598699 | GTCATTGAAAAAAAA[-/A]TTTTTAATTTTATTT | 51133 |
rs57056866 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565928 | CTTTCTTTTTTTCAG[C/T]TCATCAGTTATCGTT | 51133 |
rs57075344 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621032 | GTGAATCACATAATT[A/G]TCTTTGGAACTTGGT | 51133 |
rs57397989 | snp | C/T | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610615 | GTTATTGAATGAGGA[C/T]TGTCATTTCATTTTA | 51133 |
rs57493403 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614333 | ACTGCATCCGGCCTA[A/G]AAATAGTTTTTTCTA | 51133 |
rs57861859 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606812 | ATGACATTGTTTTCC[C/G]TATAGTGCATTTTAA | 51133 |
rs57935471 | snp | A/C/T | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586905 | GTGAAACCTGGCTGC[A/C/T]CTATGAAAATATTGC | 51133 |
rs58131515 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617366 | GCCTCTGAAGTGGGG[C/T]TCAGCTTTGTGAGAC | 51133 |
rs58411583 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570971 | TGGGGCCAGAAGTTT[A/T]AAAAAAAATTGGTGG | 51133 |
rs58759277 | snp | C/T | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617234 | AATGCGAGCTTTCCT[C/T]TGAATTCTGTGAGCC | 51133 |
rs58867901 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613564 | GAGTCTTTGTCATGA[A/G]ATCTTTGCCAGGGCT | 51133 |
rs59015398 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607741 | GCATCTTTTTTCTTA[A/C]ACACACATTATTTTT | 51133 |
rs59026507 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571677 | GCTTTGTCGCCCATG[C/G]TGGAGTGCAGTGGCG | 51133 |
rs59061106 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614035 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTTTAA | 51133 |
rs59065705 | in-del | -/CTTTCTTTCTTTCTTTCTTTCTTTCTTT | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565920 | TTTCTTTCTTTCTTT[-/CTTTCTTTCTTTCTTTCTTTCTTTCTTT]TTTTCAGCTCATCAG | 51133 |
rs59214288 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605185 | ATGGTTTTCATGTGT[C/T]AGATTTGTTTTTGTG | 51133 |
rs59417960 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605402 | TACTCCCCTGCCCCA[C/T]TGAGGAGTTTCTAAC | 51133 |
rs59592478 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614025 | TTAGAATAGTTTTTT[G/T]TTTTTTTTTTTTTTT | 51133 |
rs59635576 | snp | A/C | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610579 | AGTTATTCATTGTCA[A/C]TATTTTGACTTTGTT | 51133 |
rs59654382 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579202 | TGCTGGGTGATATTG[A/C]GTAATTACTTTTAAA | 51133 |
rs60533889 | snp | A/G | 0.108048 | 0.20579 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617038 | ATCAATCATGCCTAT[A/G]TAATGGAGCCATTAT | 51133 |
rs61346484 | snp | A/T | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605395 | AAAACATTACTCCCC[A/T]GCCCCACTGAGGAGT | 51133 |
rs61830034 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566429 | ATCACAACATTAGTA[G/T]GCTTGCCAGAGGCTA | 51133 |
rs61830035 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585444 | GGGAAAATGAAGTTG[A/T]TGTATTTTTATTTAG | 51133 |
rs61830036 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603162 | GGATTTTTTTTTTAA[A/T]TCTAGTTAAAAGGCA | 51133 |
rs71167827 | in-del | -/GAAG | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591346 | AAAGAGAGAAAGAGA[-/GAAG]GAAGGAAGGAAGGAA | 51133 |
rs71639575 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594914 | GGCTGCCAAGTCTGT[G/T]TGTTCAGATCACTAG | 51133 |
rs72739257 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587906 | TTGTTGGTTTGCTGA[A/G]TTATGTAGATCTACC | 51133 |
rs72739261 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609918 | CTAGAAGTTATGTTT[A/G]TGAGTATTCAGCATA | 51133 |
rs73085412 | snp | A/C | 0.0622301 | 0.165053 | upstream-variant-2KB, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567182 | CGTGGGGAGGAGGAA[A/C]GAAATGGAATCCCGC | 51133 |
rs73085413 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567242 | CCCCTAGCCTCCCTA[C/T]GCGCCAGCCCCGCGG | 51133 |
rs73085416 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573603 | TTGAGAGCTGCTTGT[A/G]TAATCTTAACTCTGA | 51133 |
rs73085420 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576050 | TTTATGAAATAAAAG[G/T]TTTTTTTTGTTTGTT | 51133 |
rs73085423 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577238 | AAACATAGATCAGAA[A/G]TAGATCATGCTCGCA | 51133 |
rs73085425 | snp | A/G | 0.0164332 | 0.0891434 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577637 | ATACAGGTTTCCAGT[A/G]TTAGAGAATTTACAT | 51133 |
rs73085429 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584735 | TATCTGAAAGCATGC[G/T]ATTCCAGTCAAAGTC | 51133 |
rs73085431 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587786 | CTCTAAAATCATATC[A/G]GTGAACTTTTCATAT | 51133 |
rs73085432 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589015 | CTGTGATGTCGTAAC[C/T]TACCTTTGAGATACT | 51133 |
rs73085436 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589815 | TCCATTGAAATAATA[C/T]GGCAGAATTTGTTTA | 51133 |
rs73085441 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592133 | ATTCAGTCATTTCCC[A/G]TGGGGTTCCTCTCAC | 51133 |
rs73085444 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595612 | GTGGTAAATTTTTTT[A/G]CTAGATGCATATTTG | 51133 |
rs73085451 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601608 | ACAACCAATCGAAAT[G/T]GAGAAAGGAAAGTAC | 51133 |
rs73085453 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605773 | CTTTCTTTCACCTCC[C/T]ACATAGTACAATTCA | 51133 |
rs73085455 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609264 | GATAGACATTTGTTG[A/G]GTGTGGAAGGTTCTA | 51133 |
rs73085460 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611710 | AGCTGAAATGTGATA[A/C]CATATTGGTACGTAT | 51133 |
rs73085461 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612391 | CTTGGCACAGCTTAC[A/T]ACATAGCACACATTT | 51133 |
rs73087422 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612977 | CACAACAAGGAGCCT[C/G]TTGGGGGTGAGCGGG | 51133 |
rs73087423 | snp | A/G | 0.108755 | 0.206276 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615079 | GTGCAATTTCTGCAT[A/G]ATAAAACAAATTTTA | 51133 |
rs74506048 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615731 | ACAAAAGATAGGCTA[A/G]CAAGAGAAAACATTA | 51133 |
rs74621592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585391 | TCAATTGTATATTCT[C/T]ATGAATTACAGTTGT | 51133 |
rs74724069 | snp | G/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579515 | TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG | 51133 |
rs74729818 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611646 | TTCTTTAAAAATGTT[C/T]TAATGCAAATTGAAG | 51133 |
rs74922019 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617216 | CTTTGTAATTAACTC[A/G]TAAATGCGAGCTTTC | 51133 |
rs75090569 | snp | C/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571706 | CGCGATCTCAGCTCA[C/G]TGCCAGCTCCACCTC | 51133 |
rs75181256 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618259 | AGCTCAAGAATGAGA[C/T]TAGGATAGTCTTTAT | 51133 |
rs75212936 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597713 | TAGGCTGGACAAGAA[G/T]TTGGGAGACTTGTTT | 51133 |
rs75215822 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618246 | TTCACAAACCTTGAG[A/C]TCAAGAATGAGACTA | 51133 |
rs75221520 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573442 | TGGAGAGATGAGATG[C/G]AACCTGAAGGTAATT | 51133 |
rs75328598 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578256 | TATATATTGGAGCAG[G/T]GGTTTGGCAAACTTT | 51133 |
rs75423868 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591805 | TAACTCTAGCCTCAA[C/G]TTCTTCGCCTCCTCA | 51133 |
rs75431238 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574809 | ATTGATTGTATATAT[A/G]TAGTTGATCATAGTA | 51133 |
rs75444276 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587209 | ATCTCAGCTCACTGC[A/G]ACCTCTGCCTCCTGG | 51133 |
rs75547166 | snp | A/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603998 | TAAGATTTTTTTTTT[A/T]ACTGAACTGGATTTG | 51133 |
rs75585239 | snp | G/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614957 | TTAAAACTGGTATCA[G/T]AACATTCTCTAACAA | 51133 |
rs75651965 | snp | C/G/T | 0.026567 | 0.112152 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619193 | GCTACTCAAATTACT[C/G/T]GATCAATGTGATTTG | 51133 |
rs75735880 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583511 | TACTCCGTCCTGTTT[C/T]GTCAGCGGGATCTTT | 51133 |
rs76106000 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587952 | TCATTGTATAATATG[A/G]AAAAAAATTGCATTC | 51133 |
rs76262726 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617478 | AATCGACTGCTTGCT[C/T]GGTGTTTGGTGAACC | 51133 |
rs76416573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582059 | TTAACGAAGAGTAGT[A/T]GTGTGAATTGCTGCC | 51133 |
rs76551420 | snp | C/T | 0.0456336 | 0.143994 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566976 | TCTCCAAATGTTCCC[C/T]GCATTTGCACTGTCT | 51133 |
rs76553829 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621736 | TTTAAAATTTACTAT[A/G]TTGCCAGTGGTTTCA | 51133 |
rs76608456 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569068 | ATAATCATTTACAAT[A/C]CCTACACTGGTTTCT | 51133 |
rs76678377 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580568 | TAGTGTAGACCGGTG[A/T]TTTTTTTTTTTTTAA | 51133 |
rs76692317 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582160 | ATTTAAGGATTTATT[G/T]TCTTCTCAGTGGGTA | 51133 |
rs76721467 | snp | C/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599500 | AATTAGTGGTAATCA[C/G]TGTGTGCTACCTTAT | 51133 |
rs76797300 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572522 | GTCACCCTGGCCTGC[A/C]ATCCAGTGCTATTTA | 51133 |
rs76807847 | snp | A/G | 0.103082 | 0.202275 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566260 | ATTATAACATTAGTT[A/G]TGACGAAGAAAGATG | 51133 |
rs76910316 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569141 | TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTTGCT | 51133 |
rs76916537 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572152 | ACCATAAAATGCCTG[C/G]AGATCGTACAGAAGA | 51133 |
rs76946063 | snp | A/C | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603999 | AAGATTTTTTTTTTT[A/C]CTGAACTGGATTTGG | 51133 |
rs77055124 | snp | C/G | 0.0422008 | 0.138995 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583780 | ATTTCTGCCTATTAG[C/G]GTCTTCTGCATTCAG | 51133 |
rs77217914 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593063 | CCTTTCACATAGCCC[A/C]TAATACTGAATATAG | 51133 |
rs77321280 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582438 | GTAACTCTATTCTTC[A/G]CATAGCTGTCTTAAC | 51133 |
rs77357619 | snp | C/T | 0.0265971 | 0.11221 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619169 | TGTAGGTGGTCCAAC[C/T]GAAGAAGAGCTACTC | 51133 |
rs77373647 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593456 | TTACAAGACTGATTA[A/G]AAGTTTTCAAGGTGT | 51133 |
rs77404591 | snp | A/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580569 | AGTGTAGACCGGTGA[A/T]TTTTTTTTTTTTAAT | 51133 |
rs77462261 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618571 | CCATTGTTTCCTGAT[C/T]CGTCAATGTGGATAA | 51133 |
rs77472643 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585856 | GGAACTGTAGTTCCA[C/T]AGAGTTTTGCATTTA | 51133 |
rs77696438 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600171 | TTAATTAAAAGCCTG[A/G]CCTCAGGATAGGGCA | 51133 |
rs77914839 | snp | A/C | 0.0310518 | 0.120672 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621443 | GTGTTAACAACAATC[A/C]TGATAATTAAATTAA | 51133 |
rs78141171 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615774 | ATTATACTTTTATAT[A/G]ACACGAGAGCCTTCA | 51133 |
rs78215787 | snp | A/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580581 | TGATTTTTTTTTTTT[A/T]AATTGGGAAAGTGAT | 51133 |
rs78258654 | snp | C/G | 0.0337553 | 0.125452 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620938 | ATATAGGTGAGCATC[C/G]CTTTAGATCATGGGA | 51133 |
rs78526152 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591815 | CTCAAGTTCTTCGCC[G/T]CCTCAGTTCAGGGAA | 51133 |
rs78786866 | snp | G/T | 0.0337553 | 0.125452 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621566 | ATTGTAAGAGCAAAA[G/T]AACGTTTTTGTACAA | 51133 |
rs78904210 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615622 | AGGCCTCCGTCTCAA[A/G]AAAAAAAAAAAAAAG | 51133 |
rs78939641 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605198 | GTCAGATTTGTTTTT[C/G]TGAAGGCTGGCTAGA | 51133 |
rs78940073 | snp | G/T | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614847 | TGATGAATAAATTCT[G/T]TGAGATGAATTTTTT | 51133 |
rs78946184 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588195 | TCAAATTAAAATGGT[A/G]CTTAATGAACAGAGC | 51133 |
rs78963843 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573368 | ATGGTAGTAAGCATG[A/G]ATTTTTTGGGGATAT | 51133 |
rs79035370 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611353 | AAAGAAGAAATGTGG[C/T]TAACAGAAGCTTCAA | 51133 |
rs79083369 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608760 | AGAGATAGATCATTC[C/T]ACCCCCGGCCCCATT | 51133 |
rs79119384 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617517 | CCATTTGGTCACAGA[A/T]CCCTTTTTTTTGCCA | 51133 |
rs79289600 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603945 | TTAGGAAAAGATTTA[C/T]CAAGGAAATAATGAT | 51133 |
rs79355047 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583132 | TAGTTTTTTTTTTTA[A/G]GTGAATCCAAGTTTA | 51133 |
rs79601310 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612023 | GAGTGCTACTAGAAA[C/T]AAATTGTTGGGACAG | 51133 |
rs79654782 | snp | A/G/T | 0.0452528 | 0.143452 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615899 | AGTTGTAAGTTAACA[A/G/T]AAATAGACTGAGTAG | 51133 |
rs79684542 | snp | G/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592375 | GTCCATTTTTTTTTT[G/T]GTTGTTACTGCTGTT | 51133 |
rs79700903 | in-del | -/TT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604673 | TTTTTTTTTTTTTTT[-/TT]GCTCTCTTGGCATAT | 51133 |
rs79757093 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605088 | GTGAGTTGGGTGTGT[A/C]AGTAAAGCTTGCTTT | 51133 |
rs79764223 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601704 | GCATGTTTGTGTATA[C/T]GTGTGTGCACGCGTG | 51133 |
rs79868024 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618264 | AAGAATGAGACTAGG[A/T]TAGTCTTTATCACTA | 51133 |
rs79889598 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576074 | GTTTGTTTTTTTTTT[C/T]CCTTGAGTTGCAGTC | 51133 |
rs79928550 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617396 | CCGAGTCTTCTACCC[A/G]TGTGATATGACAGAT | 51133 |
rs79969655 | snp | A/G | 0.0018496 | 0.0303542 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607969 | AAAAAGTTAAAATGA[A/G]TTTTTAAAAGTAATT | 51133 |
rs80018194 | snp | G/T | 0.0498117 | 0.149749 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567076 | GGTCATAAAGATCCG[G/T]AGATCGTTTGCCCAG | 51133 |
rs80141033 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606329 | AATAACTTTCTCTAA[A/C]GGTACCTTGCTTTGT | 51133 |
rs80285466 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605430 | AACTCTTGCTGGTTC[A/C]TCATCTTTTGCCCAG | 51133 |
rs111228517 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615577 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 51133 |
rs111276434 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571768 | CCTGAGTAAGCTGGG[A/G]CTACAGGTGCCCGCC | 51133 |
rs111281684 | snp | A/G | 0.00113716 | 0.0238178 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577628 | CAGATGATAATACAG[A/G]TTTCCAGTGTTAGAG | 51133 |
rs111306229 | in-del | -/CTA | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608442 | ATCTTCACATGTTAA[-/CTA]CTTTTATTTATTATT | 51133 |
rs111376026 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609014 | GAACATCAACTTACA[A/G]TGTAGTGAGCAGTGG | 51133 |
rs111382480 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618625 | TTATCTTTTATGAAA[A/G]TCAACTAAAAAGTCA | 51133 |
rs111428787 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598600 | ATTTGCAATCCCCAA[A/C]TTGGAAATAATGGAA | 51133 |
rs111458350 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608361 | ATTATTTTATTGCAG[C/T]GTTTTTCCTTAAAAT | 51133 |
rs111540252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572494 | CTACTCTGTATAAGC[C/T]TTGGTAGTCACAGTC | 51133 |
rs111611750 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577287 | TGGGGAGATTAAGAT[A/G]GATATGTATAGAAAT | 51133 |
rs111659220 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601560 | CAGTTCTAGTGGGCT[A/G]CAATCTAGTGATCAC | 51133 |
rs111712738 | snp | A/G | 0.106633 | 0.204807 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582797 | AAACTCCTGATCTCA[A/G]GTGATTCACCCGCCT | 51133 |
rs111808626 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585534 | TAGTGTGCAAAAGAA[C/T]GCTTCTTTTCCTTCA | 51133 |
rs111859068 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608645 | TTCAGCAAAAGGTGT[A/G]TAAGTTTAGTTTAGG | 51133 |
rs111980726 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588146 | TTTGAGGATAGTTCT[A/G]CCAAACACCCAATTC | 51133 |
rs111988932 | snp | A/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595618 | AATTTTTTTGCTAGA[A/T]GCATATTTGAGCATA | 51133 |
rs112014821 | snp | C/T | 0.109108 | 0.206518 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604935 | ATTTTTAATTAAATA[C/T]TAATTGGATACATAA | 51133 |
rs112042031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591861 | TTGGTATATTAGTCC[A/G]TTTTCACACTGCTGA | 51133 |
rs112147989 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601083 | GCCGGGATTACTGGC[A/G]TGCGCCACTACGCCC | 51133 |
rs112161168 | snp | C/T | 0.104504 | 0.2033 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618690 | ATGATGGATACAATA[C/T]GGGCCATCTCCATAG | 51133 |
rs112162610 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609545 | AGATTTGTGATATAT[A/G/T]TAATTCATCTTTCAA | 51133 |
rs112187948 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580214 | CCTTTATCTGTTGTA[A/G]ACATTTAGCAGACAA | 51133 |
rs112239365 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582131 | GGAGTTTACTTTTTT[A/G]TATGTGGTATGAGAT | 51133 |
rs112254931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613593 | CTGATGTCCAGGTTG[A/G]TATTTCCTAGGTTTC | 51133 |
rs112334310 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599578 | CCATGCATACTAATC[A/G]GTATGGTTTCTTGGA | 51133 |
rs112335175 | snp | C/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590428 | GGCCTGTACCTGTCT[C/G]CCTTCCTCTTTTCTC | 51133 |
rs112414639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601714 | GTATATGTGTGTGCA[C/T]GCGTGCACCTAAAGA | 51133 |
rs112447482 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569662 | GTGCAGTGGTGCGAT[C/T]TCGGCTCACTGCAAG | 51133 |
rs112510207 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579556 | CAGGCTGGAGTGCAG[A/T]GGTGCCATCTTGGCT | 51133 |
rs112524191 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615338 | TTAAGAAATCTATCC[C/T]GGCCGGGCGTGGTGG | 51133 |
rs112601700 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572740 | AGCCATTTTGGCTGG[A/G]GTTTGGCCTGTGTTT | 51133 |
rs112605785 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586864 | GTTTTAGAAAAGACA[C/T]GGGGAACATCTTTTC | 51133 |
rs112608703 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588726 | TAATACCAGATGGGT[A/G]CAAGTAAAACACCAG | 51133 |
rs112610178 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621092 | TTTACCAGATATTTG[A/G]TGAGGTGCTATGTTT | 51133 |
rs112614978 | snp | C/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602425 | TTGGAACTCCCCTTA[C/T]GCTGAATTGCATTTG | 51133 |
rs112682035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567952 | GTGAAGCATCTGCTC[C/T]GGGAAGGGAGAGGCA | 51133 |
rs112797770 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611077 | AATTATTAAAATTTT[A/T]TGTTTAAGTTTTAAA | 51133 |
rs112797825 | snp | C/T | 0.5 | 0 | missense | KCTD3 | GRCh38.p7 | 1:215608053 | TCCGGACGTGGACAG[C/T]AACACGATTCAGAGG | 51133 |
rs112877821 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608578 | TCATTTTGATGACAT[A/C/T]GTAATATTCATTAGG | 51133 |
rs112888435 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572318 | GCTTTAAGAAAAAAC[A/C]ACATCTACTTTTTTA | 51133 |
rs112894129 | snp | A/G | 0.108048 | 0.20579 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614174 | GTAGCTGGGATTACA[A/G]ATGCATGCCACCACG | 51133 |
rs112963547 | snp | C/T | 0.5 | 0 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619163 | CTAAGATGTAGGTGG[C/T]CCAACCGAAGAAGAG | 51133 |
rs112984134 | snp | C/T | 0.0532157 | 0.154195 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565956 | GTTAGTGTTAGTGTA[C/T]TTTATGTGTGGCCAA | 51133 |
rs113212573 | snp | C/T | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587793 | ATCATATCAGTGAAC[C/T]TTTCATATTCTGTTA | 51133 |
rs113220069 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601834 | GAAATTATAATTACT[A/G]TCTAACATCTGATAA | 51133 |
rs113221093 | snp | C/T | 0.5 | 0 | missense | KCTD3 | GRCh38.p7 | 1:215579984 | CTGCATATGCCCATT[C/T]TGCTGTGTGTTACAG | 51133 |
rs113324201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610718 | TTGAATTCCACTTCC[A/G]TCATATAGGACCTAT | 51133 |
rs113347831 | snp | C/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573847 | TTTTCCAGGTATGTC[C/T]TATAATTCTTTAGTG | 51133 |
rs113378347 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569246 | CCTGCCTCAGCATCC[C/T]GAGTAGCTGGGTCAC | 51133 |
rs113439381 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578546 | AGTTAGAAGAGCCTG[A/C]TTTTACCTGTGTTAT | 51133 |
rs113472997 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619626 | ATTGTCCTGTCTCAG[A/G]GACAATATTTATCTG | 51133 |
rs113501881 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617591 | ATTGATTATTTTGAG[A/G]TGAAAACATTAGAGA | 51133 |
rs113532245 | snp | A/C | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609012 | GTGAACATCAACTTA[A/C]AATGTAGTGAGCAGT | 51133 |
rs113533098 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614326 | GTGAGCCACTGCATC[C/T]GGCCTAGAAATAGTT | 51133 |
rs113559558 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601860 | GATAATACTCTCACT[A/G]CATCAGGTTCAAGAT | 51133 |
rs113589548 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591977 | ATCATGGCAGAAGGC[A/G]AGGAGGAGCAAGTCA | 51133 |
rs113623083 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609217 | AGACAGAGAACACAC[A/G]GAGGTTTTAATGTTT | 51133 |
rs113680622 | snp | G/T | 0.0810805 | 0.184299 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592385 | TTTTTTGTTGTTACT[G/T]CTGTTTTAAAGTGGA | 51133 |
rs113922771 | snp | A/G | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585283 | TGGCTGAAGAGGGTG[A/G]TTACAAATTACACAA | 51133 |
rs113981989 | snp | G/T | 0.5 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593736 | AGCCAAAGATCTACA[G/T]AAAACAGTATTGTAG | 51133 |
rs114079200 | snp | A/G | 0.000399281 | 0.0141238 | missense | KCTD3 | GRCh38.p7 | 1:215604132 | CTTGACTTTATATAG[A/G]TGTCAGTGGTAACTG | 51133 |
rs114116559 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613094 | ACTATGGCACATGTG[A/T]AACAGACCTGCACAT | 51133 |
rs114116630 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608497 | TTTGACATTTGAAAT[A/T]TTTTTTGTTAATCTA | 51133 |
rs114191479 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578478 | CAAACTGCTTTTTTG[A/C]AAAATTTAAGGAATT | 51133 |
rs114343835 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594691 | AGTTCTTAGTAATGT[C/T]TTGTCTTCTCGTGTT | 51133 |
rs114366365 | snp | C/T | 0.0498117 | 0.149749 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568297 | GTAGGTTTGCAGTAC[C/T]TAGTTATTTATTTTC | 51133 |
rs114722539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613195 | GTAACTTTCCTGTTA[A/G]TAGTCCATTAGGAAG | 51133 |
rs114729934 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616007 | CTTAATTTCTTTATG[G/T]CTAGCTGTTCACAGA | 51133 |
rs114800008 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614471 | GAATGTTGTTCCACT[C/T]GTTTGTGTTGTCTGC | 51133 |
rs115139035 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591812 | AGCCTCAAGTTCTTC[A/G]CCTCCTCAGTTCAGG | 51133 |
rs115142860 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599646 | CCACACAGTGGCTGC[C/T]TCCTTGCTTGTGCTG | 51133 |
rs115166450 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592743 | TATCCAAAGAAAATT[A/G]TTAGGGCTGGTATAT | 51133 |
rs115210014 | snp | A/C | 0.0437281 | 0.141251 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622220 | CTTACAGGAGATTGA[A/C]CCTTGATGCAGTGGT | 51133 |
rs115266220 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583781 | TTTCTGCCTATTAGG[A/G]TCTTCTGCATTCAGA | 51133 |
rs115296365 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577112 | ATTTCATCTGGATAA[C/T]ATAGCCCTTCCCAAG | 51133 |
rs115478347 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619390 | TAGAAAGCCATACTT[C/T]TCAAGGTACATTTTA | 51133 |
rs115503056 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604937 | TTTTAATTAAATATT[A/T]ATTGGATACATAAAA | 51133 |
rs115518398 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584232 | AAAAACTACTGATGA[A/G]ACAAATCTAATAAAA | 51133 |
rs115538444 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610138 | ACATACAGATTAGTG[C/G]AACAGAGTAGAGTCC | 51133 |
rs115662814 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612240 | CTATCTTTAAAAAAC[A/C]TGGAACTTAAATATT | 51133 |
rs115663014 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607191 | GTGTGTATATAAGAA[A/G]TTTTAGATACTTTCC | 51133 |
rs115678954 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603098 | TTAAAATGTTTACTA[C/T]TTGGCCCCTTACGGA | 51133 |
rs115727754 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611509 | AAGCACATCCCCAAA[A/G]ATAGTAAATATCTTA | 51133 |
rs115737425 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610984 | GTCTTTAAAATTTTT[A/G]TTGTAAATCTTTTTA | 51133 |
rs116075806 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617084 | AACTGAGTTCAGAGC[A/G]CTTCCAGATAGCTGA | 51133 |
rs116309520 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602926 | AATTTGACTGAAACC[A/G]TAGTAGGACTTAAAT | 51133 |
rs116435763 | snp | A/C | 0.0333695 | 0.124785 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613966 | ATTTGCTTAGGATTG[A/C]TTTGTCTATTTTATT | 51133 |
rs116490050 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598722 | TTTTTAATTTTATTT[A/G]ATGGTTAAATAGAAG | 51133 |
rs116574974 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603914 | GGAGGTGAATAGTTA[C/G]GTCTTGGAGTGAGGG | 51133 |
rs116583486 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610591 | TCAATATTTTGACTT[C/T]GTTTATGAGTTATTG | 51133 |
rs116586790 | snp | C/T | 1.78001e-05 | 0.00298324 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611804 | TAATTAATTTTTTGA[C/T]ATTTTTGTTTTCTGA | 51133 |
rs116662907 | snp | A/T | 0.0524604 | 0.153226 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612978 | ACAACAAGGAGCCTG[A/T]TGGGGGTGAGCGGGG | 51133 |
rs116986800 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576294 | GGCTGATTGCAAACG[C/T]CTGAGCTCAGGCAGT | 51133 |
rs117094222 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573500 | TTGGTGTGATGGGCT[A/G]ATTGTTGATTCTTCA | 51133 |
rs117136082 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617674 | GCCAAAAGATTTTCT[C/T]GGAGTTTTATCCTCC | 51133 |
rs117492147 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604762 | AGTTTTACTTTTAAT[A/G]TAAATTGGGTTGATT | 51133 |
rs117541551 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610097 | ATAGTGGTATTTAAA[A/G]TATATATATCTTCAT | 51133 |
rs117613872 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613421 | GTCAGATGCTTAGTT[G/T]GCAGATATTTTCTCC | 51133 |
rs117699637 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576286 | GTTGCCCAGGCTGAT[C/T]GCAAACGCCTGAGCT | 51133 |
rs137940959 | in-del | -/T | 0.00874735 | 0.0655527 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565496 | GAGAACTTTTCCTTC[-/T]CTTGAAGAGATGTTC | 51133 |
rs137944169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604633 | TTTTACCTGGTTTTA[A/G]TATACTTAAATTTAG | 51133 |
rs137954975 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567285 | CCTCCCTGACCTTTC[C/T]TTCCTCCTCCTCCTC | 51133 |
rs138048372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596720 | TGAAGGAAAGCAGAG[A/G]ATCCAAGTGATAGCT | 51133 |
rs138266571 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614717 | GATGTAGGAGCCTTT[A/G]GCAGAGACTGTGGGG | 51133 |
rs138290643 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574980 | TTATGGGCTGGGTGG[A/G]GTGGCTTATGCCTGT | 51133 |
rs138297168 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569190 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAGCCT | 51133 |
rs138324472 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589889 | AGATATTATGAATAA[A/C]GCTGCAGTTAACATT | 51133 |
rs138479455 | in-del | -/CTGTTATTTCTAA | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615041 | CTGATATCCCCCTTT[-/CTGTTATTTCTAA]CAGTAACACTGTGCA | 51133 |
rs138566432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598772 | GTAAATTGACAGACA[C/T]GTCTGAGAAAATCAT | 51133 |
rs138597417 | snp | C/T | 0.000132468 | 0.00813735 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604151 | CAGTGGTAACTGGAT[C/T]GAGATCGCCTATGGT | 51133 |
rs138629139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590299 | TCATCCTGTTACTTA[C/T]TTGTAAATGTTTTTT | 51133 |
rs138652868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609243 | TGTTTGAACTGATAC[A/G]TGAAGGATAGACATT | 51133 |
rs138685178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613112 | CAGACCTGCACATCC[C/T]GCACATGTACCCCAG | 51133 |
rs138842433 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618775 | TGATTTTTTAAAAGT[A/C/G]TTTTCTAGTATAACA | 51133 |
rs138865520 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587089 | TAATCCTCTTAAAAA[A/G]TTACTCAGGACCTGA | 51133 |
rs138888709 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569689 | CAAGCTCCGCCTCCC[A/G]GGTTCGCGCCATTCT | 51133 |
rs139068255 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587371 | CCTGATCTTGTGATC[C/T]GCCCACCTCGGCCTC | 51133 |
rs139253422 | snp | C/T | 1.65378e-05 | 0.00287552 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619146 | AATGACTATTTGTTC[C/T]CCTAAGATGTAGGTG | 51133 |
rs139260668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606465 | AGCATAATTCTGACA[C/T]GTAAAAGATGCTGAA | 51133 |
rs139278195 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610784 | TTTTTTCATCTGTAA[A/T]ATGGAGATGGTAAAT | 51133 |
rs139316731 | snp | A/G | 0.029116 | 0.117091 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613712 | GAGTTTGAATCTTCT[A/G]CAAATGGCTAGCCAG | 51133 |
rs139367552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600326 | TTTCTGTTTTTAATT[A/G]GAATGAACCTAGATT | 51133 |
rs139538101 | in-del | -/TAG | 0.0341408 | 0.126114 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571465 | ACCTGTGAAATTAGT[-/TAG]TAGTCAACTTCTATG | 51133 |
rs139552144 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570919 | TGTGTAATTTTAAGT[G/T]TGTTAGTTTTCATGA | 51133 |
rs139558874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616188 | ATTTTCTGAGACCCA[A/G]GTTTTCATATGCATA | 51133 |
rs139622332 | in-del | -/TATG | 0.0352966 | 0.128072 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619956 | GGATATAATACACTT[-/TATG]TATTTATATAGTGTG | 51133 |
rs139687381 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575465 | TATTTACTTTTCTCA[A/G]GTACCCCTGTGTGCA | 51133 |
rs139697667 | snp | A/C | 0.00841716 | 0.0643252 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215575903 | CTCTTTTTTACAGAT[A/C]TTTATTGATAGAGAT | 51133 |
rs139767647 | snp | C/T | 0.000115427 | 0.00759606 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604262 | AGTTCACCGAAGTCC[C/T]GTAACAAAAATCATG | 51133 |
rs139810472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587795 | CATATCAGTGAACTT[C/T]TCATATTCTGTTAAA | 51133 |
rs139829679 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592899 | ACTTCTGTTGTCTTC[C/T]CTGTCACTGGTGCTC | 51133 |
rs139899554 | in-del | -/T | 0.0501905 | 0.150254 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611006 | ATCTTTTTACAATAC[-/T]TTTTATGAATTGTAA | 51133 |
rs139936687 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594022 | GTGCTACCATACCCA[C/G]CTAATTTTTGTATTT | 51133 |
rs139982505 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571263 | CAATTTACCATTGAG[-/T]GGATTTGCTTTGATT | 51133 |
rs140022294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612364 | GATATTAATAACACT[A/G]ATTTGCATAATCTTG | 51133 |
rs140041193 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615352 | CCGGCCGGGCGTGGT[A/G]GCTCACGGCTGTAGT | 51133 |
rs140073774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578159 | TGAATAGGAAAAACT[A/G]CTCCTTGATTATTGA | 51133 |
rs140140772 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605461 | TTGCTGAGTGTTGGA[G/T]TGCCCTTGAGCTCTT | 51133 |
rs140328949 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606991 | TAGCCTAGAACAAAA[C/T]GTCCCCTTTTCACCA | 51133 |
rs140349105 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576369 | CCACTACGCCCAGCC[A/G]GAAAAGGTTTTTTTT | 51133 |
rs140353304 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612623 | TAGTGAATTTGCTGG[C/T]AGACGGCTGAACTAA | 51133 |
rs140415859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595717 | TTATTTTAAATGTTC[A/G]AAGTTCTATGCCTTG | 51133 |
rs140476390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589492 | CAGTGAACCTACAAC[C/T]GATAGATACTATGCA | 51133 |
rs140505671 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581111 | ATTAGCCAGGTGTGG[A/T]GATGCATGCCTGTAA | 51133 |
rs140676316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578427 | GATTTTCCATGGCCC[A/G]TAGTTTGCTGACCCA | 51133 |
rs140685751 | snp | C/T | 0.00176298 | 0.0296375 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620510 | ATCACCAAGTACTTC[C/T]GATGGAGGAACTGAC | 51133 |
rs140696602 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582915 | GTTATAGAGCAAATA[C/T]GTACCTTCTTTGTAA | 51133 |
rs140712035 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608310 | CTAAACAGAATTTTA[A/G]TGTGTTTTTCTGATT | 51133 |
rs140776978 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601335 | ATTTCCTAGAAAAGA[A/G]GTAACCTTTAGCAAG | 51133 |
rs140920472 | snp | C/G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605615 | TGTCTGGATCTCTGG[C/G/T]TGTATGTTTAATAGG | 51133 |
rs141029566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603656 | AATTCTAGGCTAGAC[A/G]TAATAAGGAATATTG | 51133 |
rs141031950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584631 | TCAGAAACCTTGTAC[A/G]GGGACCGTGTAGACA | 51133 |
rs141037534 | in-del | -/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567169 | GGGCTGGGATCGCGT[-/G]GGGGAGGAGGAACGA | 51133 |
rs141072792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606652 | TACTTTGTAAAACTT[C/G]CATTTTAACATCAGA | 51133 |
rs141109954 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613119 | GCACATCCCGCACAT[C/G]TACCCCAGAACTTAA | 51133 |
rs141142430 | snp | G/T | 1.64806e-05 | 0.00287054 | missense | KCTD3 | GRCh38.p7 | 1:215604222 | AGACAGTTGGGTCAG[G/T]TCCTCAGCTTTTTCA | 51133 |
rs141147971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616756 | CAAGAGCAAAACTCC[A/G]TCTAATGAAAAAAAA | 51133 |
rs141252284 | snp | G/T | 0.000264345 | 0.0114936 | missense | KCTD3 | GRCh38.p7 | 1:215620203 | CTATTAATTTGAACA[G/T]AAATGTAGAAAGAGC | 51133 |
rs141329923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572442 | TCAGGTGCCTGGATG[A/G]ACTTGCAAAGTTGAG | 51133 |
rs141373907 | snp | C/T | 6.61081e-05 | 0.00574888 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604157 | TAACTGGATCGAGAT[C/T]GCCTATGGTACGAGC | 51133 |
rs141522097 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613873 | TGTTTGTTTTTGTAC[C/T]GGTACCATGCTGTTT | 51133 |
rs141534827 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598854 | GAGAAAGCATTTCAG[A/G]TAGGAACAGACTAGA | 51133 |
rs141681093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604397 | TGTGAGAAAAATATA[C/G]TAAAAGAAGTACTAG | 51133 |
rs141928556 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615738 | ATAGGCTAGCAAGAG[A/C]AAACATTACAAATTG | 51133 |
rs141935194 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568027 | GTAGCTGCTGTCCTA[C/G]AATGCCAACCTTTGC | 51133 |
rs141936742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618573 | ATTGTTTCCTGATCC[A/G]TCAATGTGGATAAAA | 51133 |
rs141955486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568918 | GAAACCAGTCTTATG[A/G]AGATTTATGTCTCCT | 51133 |
rs141966619 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618811 | GCTTTCTTTCTTTCT[G/T]TCTTTTTAGTTTCAT | 51133 |
rs141973857 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572716 | TGCACAGCCTGGGAA[A/T]CATCCCTTAGCCATT | 51133 |
rs142091366 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569909 | AATTGTTAAGATAAA[A/G]TGGCTTATAAAATAA | 51133 |
rs142110285 | snp | C/T | 0.00345541 | 0.0414218 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577747 | TGTGCTCTTTTAATA[C/T]TTGGTGTTTATGATT | 51133 |
rs142128112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574872 | TTCTAATTGATTTAC[A/G]TAAGCTTTAAAAGAT | 51133 |
rs142170579 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571901 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 51133 |
rs142218047 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593692 | TATTGGCACAGGTAC[-/T]TTTTTAAAAATAAAC | 51133 |
rs142387330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589096 | GATTAAATGAGTTTT[G/T]TACATCTTTATTTAA | 51133 |
rs142406247 | snp | C/G | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215579924 | GATTTCCTGTGGATC[C/G]ACGAAAGGTGCTAAT | 51133 |
rs142437046 | snp | C/T | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215595419 | ACCAGTTGGTGGCCA[C/T]GAGTCATACAGGGAA | 51133 |
rs142495665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581746 | ACTCATGTAAAGTGA[C/T]GAAGGAAGACAATTG | 51133 |
rs142503688 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591428 | AGTGGCGTGATCATG[C/G]CTGACTGCAACCTCC | 51133 |
rs142541903 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597478 | TCATTCTCATATCAA[C/T]GTAGACAGCTTTGGA | 51133 |
rs142768579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574987 | CTGGGTGGGGTGGCT[C/T]ATGCCTGTAATTCCA | 51133 |
rs142893971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578645 | TGGGGAATTTCAGTT[C/T]TAAAGCAGTTAAATT | 51133 |
rs143079072 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613107 | TGTAACAGACCTGCA[C/T]ATCCCGCACATGTAC | 51133 |
rs143126571 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592955 | GACACTTTAAATTTC[A/G]TGAGACCATTCAGAG | 51133 |
rs143287621 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579319 | GTTGTGTAATCTTCT[A/G]TCTTCTCTGAATCTT | 51133 |
rs143393679 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574171 | ATGCTTATAGTGCTT[C/G]GTCCTAACATATAGT | 51133 |
rs143510475 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612495 | TTCCTGTCTTTATGC[A/C]GTCTCCTCAGTATTT | 51133 |
rs143619901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601621 | ATTGAGAAAGGAAAG[C/T]ACTGCTGTGGGAAAT | 51133 |
rs143630457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580759 | TATCACTGTTGAGTT[C/T]GGTTAAGAAAAATAG | 51133 |
rs143747914 | snp | C/G/T | 9.89567e-05 | 0.00703346 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619253 | CAGTCCAGCAACTTC[C/G/T]GTAGTTCAGCATAGC | 51133 |
rs143816714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618335 | TCCGGCCTACTAGGA[A/G]GCTCATCTAAGCTTC | 51133 |
rs144004725 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605492 | TCCTGGACTCTGTAT[G/T]CTTTATCTGCACTTT | 51133 |
rs144128335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619573 | AAGGAAATTAGGAAA[A/G]TTACATGTCACCTTG | 51133 |
rs144184742 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571596 | TTTTCCTTACAAATT[G/T]TAAAGTTGTATGTGG | 51133 |
rs144199183 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594654 | TATAATTGGTTGCAG[-/T]TTTTTTCTCTACTAA | 51133 |
rs144344240 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616620 | ACAAAATTAGCCAGG[C/G]CTGGTGGCACACGCC | 51133 |
rs144378155 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620727 | CAAGATAAAATTGGA[C/G]TTCATTTAGTATCTT | 51133 |
rs144420811 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599033 | CATAGAATAGTGACA[C/G]TTTGCCTGTCATTAG | 51133 |
rs144495153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583675 | CATGTTTTCCCCTTC[C/T]CTTTTACAAGGGTAC | 51133 |
rs144526691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590459 | CATCTCTCCCTTGCT[C/T]GCTCCCTCTTCCTCC | 51133 |
rs144537042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588258 | AAGGTGCTTTTCCTT[G/T]ACATAGCCATAGTAC | 51133 |
rs144589605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575623 | CCAAAGGTATCAATA[C/G]AAGTGATTTTATTAG | 51133 |
rs144623573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613445 | TTTCTCCTATCCTGT[A/G]GGTTGTCTGTTTACT | 51133 |
rs144686781 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597922 | ATTGTCTTGACTGCT[A/G]TCTTAACTGTGGTCT | 51133 |
rs144747955 | snp | A/G | 3.33367e-05 | 0.00408255 | missense | KCTD3 | GRCh38.p7 | 1:215611918 | TCTCATCGACTGGAA[A/G]AAGGTAACACTTTAT | 51133 |
rs144851808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605339 | GTAATTGTTTGTGGT[A/G]TAAGTATGCCTTGCT | 51133 |
rs144952401 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612950 | CACATGGACACATGG[A/G]AGGGAACAACACACA | 51133 |
rs145066876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618658 | AAAATCTTTTTTTGA[A/G]GTTGAGTATTATCCT | 51133 |
rs145091964 | snp | A/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606527 | CTGAGAAAATGGGCC[A/G/T]TTTTGAAGGGTTATT | 51133 |
rs145110049 | snp | C/T | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215604213 | AACACCCAGAGACAG[C/T]TGGGTCAGGTCCTCA | 51133 |
rs145160486 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572622 | AATAAAAAAAAGTAA[C/G]CAACTTCCACGTTTT | 51133 |
rs145226766 | snp | A/G | 0.00319167 | 0.0398202 | missense | KCTD3 | GRCh38.p7 | 1:215586638 | TTGCCTCAGAGAGTA[A/G]CATCATCTTGTGGAG | 51133 |
rs145270663 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600775 | AAATTATTGGAAATC[-/T]TTTTAGACTTGTATG | 51133 |
rs145413712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573291 | AGTGGTATCAAGAAA[A/G]ATGGACGGATCTTGA | 51133 |
rs145485481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594750 | TTTTGAATTAATTAA[A/G]TGGAGATTGCAGTGC | 51133 |
rs145506124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581592 | TCTTTTCCAGAACCA[C/T]CACATTATTACGCAA | 51133 |
rs145513665 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566264 | TAACATTAGTTGTGA[A/C]GAAGAAAGATGACAA | 51133 |
rs145524446 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601070 | AGCCTCCCGAGCAGC[C/T]GGGATTACTGGCATG | 51133 |
rs145709170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574944 | TAGGTGTTGGTATAA[A/G]TTTCCATAAAAAGTT | 51133 |
rs145734442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601603 | AGGAGACAACCAATC[A/G]AAATTGAGAAAGGAA | 51133 |
rs145763343 | in-del | -/ATC | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604912 | TTGTAGTTCTTCATA[-/ATC]ATATAAAATTTTTAA | 51133 |
rs145828197 | in-del | -/CT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591040 | AATTTTAGGGCAGGG[-/CT]CTCCTTTTCAAGGCT | 51133 |
rs145834170 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594388 | GCTTAGGCATTGCTG[G/T]GTCTTTTGCTACTGA | 51133 |
rs145951993 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587773 | TTCTTTATCAAAACT[A/C]TAAAATCATATCAGT | 51133 |
rs146073815 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612162 | TGATAGAATAAGAAC[A/G]CAGTGAACTTTTTTT | 51133 |
rs146084832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615297 | AAGAAAAAACCTTGT[A/G]GAAAATTTTAAATAA | 51133 |
rs146159946 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593754 | AACAGTATTGTAGAG[A/G]TGAGACTTATTTCCC | 51133 |
rs146198746 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590215 | ATCGTTTCCTGTACT[G/T]AATGACCGTTTGTAT | 51133 |
rs146224994 | snp | C/T | 0.000132608 | 0.00814166 | missense | KCTD3 | GRCh38.p7 | 1:215579093 | CCCGGGGAAATGGTA[C/T]ACAGCCTGTTCTCTC | 51133 |
rs146274541 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615817 | AAAGACACAAGGAAA[A/C]GTGTCCATTTTTATG | 51133 |
rs146314915 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618821 | TTTCTGTCTTTTTAG[C/T]TTCATAGCTTCTTTT | 51133 |
rs146327211 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570104 | CACTGTAAGAGAAAA[A/G]TCCTGATATGATTGC | 51133 |
rs146620027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584053 | GCTGATATGGAGTTG[A/G]AACCAAGCTGATGTG | 51133 |
rs146740007 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606965 | AGGAAATGATTTCCC[A/G]TGAAACTAAATAGCC | 51133 |
rs146746031 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612526 | GTTTGTGAATGCTGC[A/C]CTTATGCTTCCATTA | 51133 |
rs146868008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578374 | GTTTAACTGTAACCA[C/T]TACAACTTTATTTAC | 51133 |
rs146908156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613293 | TGTGGTGTGATCTCA[A/G]CTCACTGCAACCTCC | 51133 |
rs146917970 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616951 | AGAAGGTTGGCACTT[C/T]CAGCCCCACCCAGCA | 51133 |
rs147023449 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585823 | AATACATTAGCTTTT[A/T]CATATGGGTAGTCAT | 51133 |
rs147061896 | snp | A/G/T | 0.0174175 | 0.0916809 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589676 | TTTATCTAGAATTTC[A/G/T]TGAGTAGAATTATAT | 51133 |
rs147122424 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568075 | GAGAACCATTACACA[A/G]CCTTCCTTACCTCAT | 51133 |
rs147195597 | snp | A/G | 0.000478781 | 0.0154648 | missense | KCTD3 | GRCh38.p7 | 1:215608130 | ATACTATCCCTGGAG[A/G]AGACAGAAAGTCATG | 51133 |
rs147203723 | snp | C/T | 0.000118956 | 0.00771127 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580940 | ATATTTTCCTTGTAG[C/T]AATGATTAAGTGCAG | 51133 |
rs147213797 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587082 | AACCCCTTAATCCTC[C/T]TAAAAAGTTACTCAG | 51133 |
rs147310596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605504 | TATTCTTTATCTGCA[C/T]TTTCCTAGTTATTTG | 51133 |
rs147320470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610470 | CAAAGAAGGTATGAA[G/T]AATAGGTTATGGGTC | 51133 |
rs147583803 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572690 | AATAGATGGATGATA[C/T]AGTGTATACATGCAC | 51133 |
rs147593861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576293 | AGGCTGATTGCAAAC[C/G]CCTGAGCTCAGGCAG | 51133 |
rs147684671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594816 | AAAGGCCCGAATGTT[G/T]GTTTTTAGTATCATG | 51133 |
rs147788236 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616755 | ACAAGAGCAAAACTC[C/T]GTCTAATGAAAAAAA | 51133 |
rs147798240 | snp | A/G | 0.0103295 | 0.0711199 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621904 | TTAAAAAAAATGGGG[A/G]GAGGGAGAACTTAAT | 51133 |
rs147948403 | in-del | -/G | 0.00993419 | 0.0697739 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616106 | TCTGTGAGCCACCTT[-/G]GGGGAAAAAGAAGAT | 51133 |
rs147958786 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617112 | TGAAAACCTGGAGGT[G/T]CTGAAGGGTGGCGTG | 51133 |
rs148000300 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608240 | GAAGCATATCAACTA[A/G]TAAAACCACAAAAAT | 51133 |
rs148032050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590956 | AATTAAATTACTAAA[A/G]GATCTTGAACCTGTT | 51133 |
rs148147361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618351 | GCTCATCTAAGCTTC[A/G]TATTCTATTCCTGTA | 51133 |
rs148157165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568843 | TACTTCGTTCTTAGG[C/G]TTTTTCCTCTTCCCC | 51133 |
rs148306152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579441 | ACTTTGCCATTGTAG[C/T]ATGAACACATAATGG | 51133 |
rs148358910 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574736 | CTGTGATGTCTCTTC[A/G]ATTTTTGATGTGCTC | 51133 |
rs148400092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599694 | AGTTGTAACTCACTG[G/T]AACTCTGCTTATCCT | 51133 |
rs148407019 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581603 | ACCACCACATTATTA[C/T]GCAAAATTTAACTCA | 51133 |
rs148471152 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615825 | AAGGAAAAGTGTCCA[A/T]TTTTATGCTTAGGTT | 51133 |
rs148521111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611557 | ACTGTTAATGTGGCA[C/T]CTTAGGAAATTTTTT | 51133 |
rs148547642 | in-del | -/G | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567636 | AGCCCCGGGCTCGGC[-/G]GGTCCCGGCTGGGGA | 51133 |
rs148554694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594717 | GTGTTTTTTAATCCT[A/G]AAGCCTGATATAGTG | 51133 |
rs148669072 | snp | A/C/T | 0.00341239 | 0.0411654 | missense | KCTD3 | GRCh38.p7 | 1:215620593 | ATAAAAAAAGTGATT[A/C/T]TTCAGGTCAGGAGTA | 51133 |
rs148678616 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571890 | CCCGCCTCGGCCTCC[C/G]AAAGTGCTGGGATTA | 51133 |
rs148720921 | in-del | -/TATA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617776 | TTTACATTGTCCCAC[-/TATA]TATATATATATATAA | 51133 |
rs148839444 | snp | G/T | 0.0422008 | 0.138995 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566646 | GTATTATAGTATTCC[G/T]ATTTAAAAAATATTT | 51133 |
rs148902817 | in-del | -/AGAT | 0.0475351 | 0.146656 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622212 | TCTTTTGCTTACAGG[-/AGAT]AGATTGAACCTTGAT | 51133 |
rs148933987 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585640 | TAGATACTTCATAGT[C/T]CAACTCATTCATTAT | 51133 |
rs148938818 | snp | A/G | 0.000115362 | 0.00759393 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215618928 | TACTACAATATCCTC[A/G]TTTACAGTGAGGGAA | 51133 |
rs148953183 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598529 | CTAAAATAACCTCCC[-/A]AAACTTATAAACTTC | 51133 |
rs149017450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617157 | GGAAGCTCTATGCTC[C/T]TTCCCACACACCTTA | 51133 |
rs149070921 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612990 | CTGTTGGGGGTGAGC[A/G]GGGCCGGGGAGAGAG | 51133 |
rs149176229 | in-del | -/TAATATC | 0.0422008 | 0.138995 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580469 | ACAAGTGGTATAGTT[-/TAATATC]TAATATGTGAAACTT | 51133 |
rs149195733 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588616 | TAGAATAAGCCATGA[A/T]ATTCATATAAGTTTT | 51133 |
rs149258039 | snp | A/G | 3.29669e-05 | 0.00405984 | missense | KCTD3 | GRCh38.p7 | 1:215619219 | ATTTGAGCACATCTC[A/G]CTGTGCTACTCCTAA | 51133 |
rs149298621 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590435 | ACCTGTCTCCCTTCC[G/T]CTTTTCTCCATCTCT | 51133 |
rs149336340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575547 | TTTATTCATGTTTTC[A/G]AAGTATTAATTGAAT | 51133 |
rs149394151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610864 | TTTGGAAAGCATTTA[C/T]GGTGGCACATAGTAA | 51133 |
rs149448721 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604874 | TTGTAGAGATTATTT[C/G]AAGAAAATAAGCTTT | 51133 |
rs149544622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619420 | AAATTCAGACATTAT[A/G]TTAACTTTTTAACAG | 51133 |
rs149700897 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581205 | GAGCTGATAGCTCAC[C/T]ATTGTACTCCAACCT | 51133 |
rs149712042 | snp | C/T | 0.0138799 | 0.0821421 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565528 | CCTAATTTTTAAGTA[C/T]AGTATAATAAAATGA | 51133 |
rs149751728 | snp | C/T | 3.295e-05 | 0.00405881 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586627 | AATGGTTGCTGTTGC[C/T]TCAGAGAGTAGCATC | 51133 |
rs149827340 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594058 | AGAGATGGGGTTTCA[A/G]TGTGTTGCCCAGGCT | 51133 |
rs149918874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612926 | AACAAATTTTTTTGA[C/T]GATGAGAACACATGG | 51133 |
rs149975485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606526 | TCTGAGAAAATGGGC[C/T]GTTTTGAAGGGTTAT | 51133 |
rs149998746 | snp | A/C/T | 0.000181941 | 0.00953623 | missense, synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620462 | TGAAGGGGGAGGATT[A/C/T]CTTGGAAGAAAGAAA | 51133 |
rs150000240 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601312 | AATGAGACTTTGTTT[C/T]CCTTGCCATTTCCTA | 51133 |
rs150077901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608995 | AAATTTTAAAAAGTG[C/T]GGTGAACATCAACTT | 51133 |
rs150080026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572721 | AGCCTGGGAAACATC[A/C]CTTAGCCATTTTGGC | 51133 |
rs150228160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585131 | AAGAAAGAATTCAGG[A/G]TGAGTCCTTAGAGTA | 51133 |
rs150322454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604471 | TTCTTTGAGCTGGTC[A/G]TGGTGGCTCATGCCT | 51133 |
rs150375925 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595988 | TAAAATGAAAAGTGG[A/C]CTGGAGGTCAGGAGG | 51133 |
rs150444410 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614146 | CACACTATTCTCCTG[C/T]GTCAGTTCCTGAGTA | 51133 |
rs150492045 | snp | A/G | 3.30841e-05 | 0.00406706 | missense | KCTD3 | GRCh38.p7 | 1:215601891 | GTTGTTCCTATAACT[A/G]GTTATGACACTGCTG | 51133 |
rs150561943 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588443 | TCTTTAAATCTTTGA[-/T]TTGGCCTTTTATGTT | 51133 |
rs150604147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575017 | AGCACTTTAGGAGGT[C/T]GAGGCAAGTGGATTA | 51133 |
rs150657039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215569320 | GAGACGAGGTTTAAC[C/T]ACGTTGACCAGGATG | 51133 |
rs150751052 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587354 | CAGGATGGTCTCGAT[A/C]TCCTGATCTTGTGAT | 51133 |
rs150801449 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580563 | AAGAATAGTGTAGAC[C/T]GGTGATTTTTTTTTT | 51133 |
rs150846499 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605798 | AATTCATCAGTAAGT[C/T]CTGTTGGTTTTGCTG | 51133 |
rs150900846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600216 | TTTGAGATATTTCTT[A/G]TGTAACTCATAACTG | 51133 |
rs150996717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616083 | CTTTGGGGAAAGAGC[A/G]TTCTGGTTTCTGTGA | 51133 |
rs151023955 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619069 | CAAAAGTGAAGATAA[A/G]GGTAGGTTCTCATAC | 51133 |
rs151078062 | snp | A/G | 3.29848e-05 | 0.00406095 | missense | KCTD3 | GRCh38.p7 | 1:215620512 | CACCAAGTACTTCCG[A/G]TGGAGGAACTGACTC | 51133 |
rs151086775 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599911 | AAAAAAAAAAAAAAA[-/G]AATGTATCCAAAGGG | 51133 |
rs151156017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577861 | TTGTGGATTTTCATA[C/G]TAAAAAGATGTTGTC | 51133 |
rs151206089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572403 | TTTATCAAGATATGT[A/G]AAATATTATGAGCCA | 51133 |
rs151225147 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595663 | AGTTACTTTGGAAAA[C/T]AAGTGAGTTTTTTAA | 51133 |
rs151253564 | snp | C/T | 1.65649e-05 | 0.00287788 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215601884 | TCAAGATGTTGTTCC[C/T]ATAACTAGTTATGAC | 51133 |
rs151274459 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589161 | TTTTTTCTGAGACAG[G/T]GTCTTGCTCTGTCAC | 51133 |
rs180707139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574390 | AATTTTTTTAGATCA[A/G]TAATTGAAACTTTAA | 51133 |
rs180716157 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615599 | CACTCCAGCCTGGGC[A/G]ACAGAGCAGGCCTCC | 51133 |
rs180725591 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593845 | TATTTAAGTGCTAGA[A/G]TTGGAATACAACTTT | 51133 |
rs180954949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611625 | AATTTAGAAATAATT[C/G]TGTATTTCTTTAAAA | 51133 |
rs180983963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589033 | CCTTTGAGATACTTC[A/G]TTAGATTTTTCATTT | 51133 |
rs181174138 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593219 | TTCATTTCTTAACCA[A/G]TTCTGGGCAACGGAC | 51133 |
rs181193137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614486 | TGTTTGTGTTGTCTG[A/C]TTTCTTCGAGCAGTG | 51133 |
rs181207247 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573631 | TGAATTGAAAGTAGC[A/G]ACGTTTAAAAATATT | 51133 |
rs181220251 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584610 | TCTTTACTTACCCCA[A/G]ACAGGTCAGAAACCT | 51133 |
rs181364519 | snp | A/T | 0.0023933 | 0.0345097 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622258 | TGTCTACTCTGACAC[A/T]AATTTCTCAGATTGC | 51133 |
rs181404911 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588481 | GTCTATGGCAGAGAA[A/G]AATGCAATGGTCACT | 51133 |
rs181415459 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611105 | AAACAAAAACTTTTT[C/T]TCTTTACATTGTTGT | 51133 |
rs181428409 | snp | A/C | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568908 | CAGTTGTATAGAAAC[A/C]AGTCTTATGGAGATT | 51133 |
rs181444192 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579256 | TATCCAGATTTATCA[C/T]TTATATCTTGGAAAG | 51133 |
rs181464094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588169 | CCCAATTCTGAATAA[A/C]CATAGTCATCTCAAA | 51133 |
rs181476582 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600141 | TTCCTGGTATAAAAT[A/G]TTTTGGCATTGGCTT | 51133 |
rs181626450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610449 | GGGAGGTGGGGGAAG[C/T]GAGGGCAAAGAAGGT | 51133 |
rs181639567 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580612 | AGGACTCTTAGTTCA[A/G]AATCACTGTACTCAT | 51133 |
rs181799188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604769 | CTTTTAATATAAATT[A/G]GGTTGATTATATTAT | 51133 |
rs181802775 | snp | A/G | 1.777e-05 | 0.00298072 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579863 | GGCTGTAATTTGCCA[A/G]CCCCCGGTTTAGAAT | 51133 |
rs181810550 | snp | A/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599030 | ATTCATAGAATAGTG[A/G/T]CAGTTTGCCTGTCAT | 51133 |
rs181988106 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616212 | ATGCATACAAATGTT[G/T]ATTTGTTTTATTTGA | 51133 |
rs182003737 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575287 | AGTTACCAATTATGT[A/G]TTTTACATTTTTAAG | 51133 |
rs182019353 | snp | A/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595565 | ATTCGTACTGTTTCT[A/G/T]GTTTTGGTTATACAA | 51133 |
rs182096439 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215605609 | ATCCAGTGTCTGGAT[A/C]TCTGGTTGTATGTTT | 51133 |
rs182101336 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215585546 | GAACGCTTCTTTTCC[G/T]TCATCTTCTATATTC | 51133 |
rs182328899 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583864 | GACAAAAAGTGATGA[A/C]TGAAAAATTAATAAG | 51133 |
rs182343712 | snp | C/T | 1.65315e-05 | 0.00287498 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215602128 | AGATAATGATCTTCT[C/T]GTAACTGAACTGTAT | 51133 |
rs182346478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581924 | TTACAAAACCTTTAA[A/G]AAAAGAGTAGTACAG | 51133 |
rs182556210 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596973 | TTCTCTGTGACAGAA[A/G]GGTAAGGAAGGAGTA | 51133 |
rs182619452 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577084 | CTTAACTTTACTACT[A/G]TGAAGTAGCATCATT | 51133 |
rs182630027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612812 | AATAGATGTACAGTA[A/G]AAGTTAATTTCCTCT | 51133 |
rs182653384 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591645 | AGGCGTGAGCCACCG[C/T]GCCCGGCCAGCAGCC | 51133 |
rs182656163 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570149 | AACTGCTGTGGCATA[G/T]AATTGAAGTTCTGAA | 51133 |
rs182716665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570603 | TTAGTCTATTAAAAT[A/G]TAAAGTGACAGACAG | 51133 |
rs182726087 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612277 | CCCATATAAATCTGT[A/G]TACATTATTGATGTT | 51133 |
rs182727522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590562 | TCCATTCTTCAGTTT[A/C]GATATCTTTTATTGA | 51133 |
rs182928308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616419 | AAATTTTAAAATCTG[A/T]TAATGCCCATGAAAA | 51133 |
rs182946143 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586884 | AACATCTTTTCACCA[C/T]TTTAAGTGAAACCTG | 51133 |
rs182966543 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596521 | AGGGGACAGGATAGA[C/T]AACCAAGAGCCAAAG | 51133 |
rs183194296 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581115 | GCCAGGTGTGGTGAT[A/G]CATGCCTGTAATCCC | 51133 |
rs183396858 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571504 | CTAAAGTACCCCTTA[C/G]TGTAGTTTACATTTA | 51133 |
rs183403195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600288 | AAGAGCTTAGAGGAA[G/T]GATTATTTCCAAGTT | 51133 |
rs183426715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603231 | CTTTTGTAGTGGCAG[C/G]GGGATTTTAAGGCAT | 51133 |
rs183501453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607865 | CAGTTTTCTCACTTT[C/T]GTTAAGTAGTCACAA | 51133 |
rs183510954 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616901 | TGCCAATGAGTTGAC[C/T]GATGGCAGGTCACCA | 51133 |
rs183535121 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576194 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTGT | 51133 |
rs183591137 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608783 | GCCCCATTTGAAAGA[A/T]TCTCACTGTCCTTAT | 51133 |
rs183606493 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566182 | CATCCCACTTGCTAC[C/G]TATGTAATTTTGAGC | 51133 |
rs183653941 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603719 | CTTGGCATGGCAGAT[A/T]TATGAATTCTTTAAA | 51133 |
rs183656721 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582357 | TCATAATAAGTTTCA[A/G]AATCTCACAGGGCAT | 51133 |
rs183659531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583479 | GCCATCTTGGTTTCA[A/G]TTTTGGCTGGCTTCT | 51133 |
rs184025577 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586276 | TTCAAGTCGTTATAT[A/G]TGCTATGTATGCAAG | 51133 |
rs184065084 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615223 | AAAGATTTTGTTTAA[A/G]GACAGTTCAGGCTCT | 51133 |
rs184081217 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583238 | TTACAGTTATTTCTT[A/G]ATTATATACTAAATA | 51133 |
rs184195443 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606988 | AAATAGCCTAGAACA[A/G]AATGTCCCCTTTTCA | 51133 |
rs184374228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613278 | GCCAGGCTAGAGTGC[C/T]GTGGTGTGATCTCAG | 51133 |
rs184401571 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621061 | GTCTCCCAACACTTA[C/T]TGTGATTGCAAAGTG | 51133 |
rs184416788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572486 | TTCTGACACTACTCT[G/T]TATAAGCCTTGGTAG | 51133 |
rs184428499 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579720 | AGCCAGTATGGTCTC[A/G]ATCCCCTGACCTCAT | 51133 |
rs184495264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593125 | ACATTGTTTGTTATC[A/G]TCATTAAAGTACTAT | 51133 |
rs184503557 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613714 | GTTTGAATCTTCTGC[A/G]AATGGCTAGCCAGTA | 51133 |
rs184508701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592303 | AGTGTGTTTCTGTCT[C/T]TCAGGTCCTCTGCTG | 51133 |
rs184527655 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572567 | AGATGGGAATGGGAA[A/G]TAGGATGTATTTTGA | 51133 |
rs184570332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618467 | AAACTCCCTCAACTC[C/T]TTTGAAGTAGGCTGG | 51133 |
rs184630096 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593493 | TCACTGGTCTTGAGT[A/G]TAGTACAGTTCTGAA | 51133 |
rs184776872 | snp | A/G | 0.00076327 | 0.0195206 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573851 | CCAGGTATGTCTTAT[A/G]ATTCTTTAGTGTATA | 51133 |
rs184998974 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603420 | CTGAATTTTTTCCTA[C/T]CTAAATTTGCAATGG | 51133 |
rs185013839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597387 | GTTACATAGCCTAAT[A/G]GCAATTTTTAGGCAC | 51133 |
rs185202717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578895 | TTGGAAGATGTATTT[C/T]GGCTTTAATGAAATT | 51133 |
rs185241871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588570 | CAAACGTTGCTTTGC[A/G]TCATCAGTGTAAATG | 51133 |
rs185253377 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581142 | TCCCAGCTACTCGGG[A/T]GGCTGAGGCAGGAGA | 51133 |
rs185261909 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611119 | TTTCTTTACATTGTT[G/T]TTCAGGATCTTTCTA | 51133 |
rs185314141 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215597607 | CTGAGTGATAGCCTA[C/G]CCTCTAAATACACAG | 51133 |
rs185495312 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585812 | AGGTATTAAAGAATA[A/C]ATTAGCTTTTACATA | 51133 |
rs185505233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215605633 | TATGTTTAATAGGCA[G/T]CTCAAATTTAAGTTG | 51133 |
rs185557589 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604982 | TTTCAAGTTTAACGA[A/G]TAGTACTTTCTGATT | 51133 |
rs185563628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609879 | GGTATGAAGATATAC[C/T]TGGTTTCTGGAGAAA | 51133 |
rs185566601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584841 | TGTAAGTTAAGAATA[C/T]TCACAAATAGTTTCC | 51133 |
rs185670044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587424 | GTGAGCCACCATGCC[C/T]GGCCTTTCTGTAGGT | 51133 |
rs185778519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616215 | CATACAAATGTTGAT[C/T]TGTTTTATTTGAAAC | 51133 |
rs185795554 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575454 | GCAGTGTGCAGTATT[A/T]ACTTTTCTCAAGTAC | 51133 |
rs185806972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215595893 | ATACCTGATTCTTAA[A/G]GGAAAGAGGAAAAAA | 51133 |
rs185811331 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566633 | AGCAGGGCATCAAGT[A/G]TTATAGTATTCCGAT | 51133 |
rs185857808 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600336 | TAATTAGAATGAACC[A/T]AGATTCTGTGCTTTT | 51133 |
rs185920743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568966 | TTTTCCTAAAATCAC[A/G]TTAAAATATTGGAAG | 51133 |
rs185964254 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574849 | TTATTACTGGCTGCC[A/G]TTTCCCTTTCTAATT | 51133 |
rs185972704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615958 | GGCATTCCTTTCTCC[A/C]AGGGATGGGGCAGAA | 51133 |
rs186099938 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588196 | CAAATTAAAATGGTA[C/T]TTAATGAACAGAGCA | 51133 |
rs186103960 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594174 | CGATTATAACATTTT[G/T]AAGCTCAAGTGATCA | 51133 |
rs186121905 | snp | G/T | 0.00318978 | 0.0398085 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621915 | GGGGGGAGGGAGAAC[G/T]TAATATATGTGGAAA | 51133 |
rs186134870 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568163 | GATGTTGGAGATGAA[C/G]TTGCTTTCCTTTCTC | 51133 |
rs186150855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599274 | GGGAAGAAATGGAAT[C/G]CATTAAGCAGTGATT | 51133 |
rs186155074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580164 | ATTTAGTGTACTTTT[A/G]TTTTCACAGCTAATT | 51133 |
rs186686550 | snp | C/T | 0.0138293 | 0.0819965 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604320 | AAAATGATTTCATTA[C/T]ACTGGTAAGGAACTT | 51133 |
rs186772760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609548 | TTTGTGATATATATA[A/G]TTCATCTTTCAAGAG | 51133 |
rs186776895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580754 | TTGTTTATCACTGTT[C/G]AGTTCGGTTAAGAAA | 51133 |
rs186855933 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565231 | ATATTTTTCATTACT[G/T]GTTTTCTCAATTTAT | 51133 |
rs186866255 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607956 | TAGATGATAGTGAAA[A/C]AAGTTAAAATGAGTT | 51133 |
rs186867519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586887 | ATCTTTTCACCACTT[A/T]AAGTGAAACCTGGCT | 51133 |
rs186899217 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566765 | GCGTGTGTCTAACAT[A/T]AGTTGAGTGCTTACT | 51133 |
rs186934663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584492 | CTTGAGCCTTGCCAT[C/G]GGTTTATCATTGCCT | 51133 |
rs186975238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577102 | AAGTAGCATCATTTC[A/G]TCTGGATAACATAGC | 51133 |
rs187034530 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589454 | CCAATTTCTTTTTGT[C/T]TAAACTCTTGGGTAT | 51133 |
rs187090161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612998 | GGTGAGCGGGGCCGG[A/G]GAGAGAGAGAGCATC | 51133 |
rs187155295 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600207 | ATTGAGTTCTTTGAG[A/T]TATTTCTTGTGTAAC | 51133 |
rs187239375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570180 | GTGATAGAGTAAAAC[C/T]CAAAAGGAGAGTTTG | 51133 |
rs187245272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612060 | GTTATCTCATAATCA[C/T]AACTCAAAATTAAGA | 51133 |
rs187508352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612398 | CAGCTTACAACATAG[A/C]ACACATTTTTTTTTT | 51133 |
rs187524611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570710 | TACTTACAGTGCAGA[A/G]TAAATAACTAGTTAG | 51133 |
rs187537304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571991 | TAGAAAATTTATTTT[A/G]GAGACTAAGGCACTT | 51133 |
rs187538197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215590766 | GTTTAATTTGTTAAA[G/T]TATTTGTCTGCTAAT | 51133 |
rs187749944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616803 | GTGATATTGTGAAAT[A/G]CATATTTGGTCTTTG | 51133 |
rs187786011 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591833 | TCAGTTCAGGGAAAT[A/C]ATCTGTCTTTATTTG | 51133 |
rs187850042 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596876 | ATGGAGATTATTTCC[A/G]GTCCCATAAAAGTCA | 51133 |
rs187968570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597413 | GGCACTGCTTCCCAA[A/G]TTGATATTTTAAATT | 51133 |
rs187978963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577906 | TAAAATTTTCCTTTT[C/T]TTTCCTTATCCTCTT | 51133 |
rs187992862 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616995 | GGAGAGGAGCCGAAG[G/T]CTAAGTTGATCAATG | 51133 |
rs188028113 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596999 | GAGTAAAGAGAAAGA[C/T]GTTGAAGAATATTAT | 51133 |
rs188091849 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616498 | GGGTGCGGTGGCTCA[C/G]ACCTGTAATCCCAGC | 51133 |
rs188133828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576575 | AACACAAATAGTTTC[A/G]AAATAGAATAAGAAA | 51133 |
rs188276317 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579734 | CGATCCCCTGACCTC[A/G]TGATCCGCCCGCCTC | 51133 |
rs188300434 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598739 | TGGTTAAATAGAAGC[A/G]CAGCTAAAAGAAAAT | 51133 |
rs188301387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607098 | GCCAAAATTAAATTT[A/C]TTTCTAAAGTTTTGT | 51133 |
rs188498691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568270 | TTGAAAGATTTCTGT[C/G]ATGGGAGTGCAGTAG | 51133 |
rs188530450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582750 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 51133 |
rs188566956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586281 | GTCGTTATATGTGCT[A/G]TGTATGCAAGTATAC | 51133 |
rs188584962 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592347 | ACCTAAAAACAGTTG[C/T]TTCATATATTTTGTC | 51133 |
rs188622071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583320 | CTGAATGTTCCTCCC[C/T]TTTTTAGACCATATA | 51133 |
rs188632299 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603483 | AAGACACAGCTGAAC[A/C]TTAGATGATTAGAAG | 51133 |
rs188663331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588234 | TAGCTCTTTGCTCCA[A/G]CATTTGTGAAGGTGC | 51133 |
rs188672013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610734 | TCATATAGGACCTAT[A/G]AGAACTTTGGTTAAC | 51133 |
rs188831456 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603238 | AGTGGCAGGGGGATT[C/T]TAAGGCATGAAAAAT | 51133 |
rs188859775 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613409 | TATTAGACCTTTGTC[A/C]GATGCTTAGTTTGCA | 51133 |
rs189152126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583517 | GTCCTGTTTTGTCAG[C/T]GGGATCTTTGTGACC | 51133 |
rs189197315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593161 | AGAATCCCTAAAATT[A/G]TATACAACGTAAAAT | 51133 |
rs189215539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613715 | TTTGAATCTTCTGCA[A/G]ATGGCTAGCCAGTAA | 51133 |
rs189232992 | snp | A/G | 0 | 0 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573266 | ACTATTACAGGGAAG[A/G]TAAAACCTGAGTGGT | 51133 |
rs189282012 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621206 | TTAATTTAGTCGTGC[A/G]TCATTTTCTGATTCT | 51133 |
rs189307967 | snp | A/G | 3.43059e-05 | 0.00414147 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604103 | ATCGTTCCATAATGT[A/G]TCACCTGTCAACTCT | 51133 |
rs189337025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587236 | CTGGGCTCAAGCAAT[G/T]CTCCTGCCTCAGCCT | 51133 |
rs189350100 | snp | A/G | 0.00478085 | 0.0486577 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622214 | CTTTTGCTTACAGGA[A/G]ATTGAACCTTGATGC | 51133 |
rs189388525 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599387 | AAAAAATAATGATAA[C/G]TTTACAGGTATAGAG | 51133 |
rs189393880 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598083 | GTTAATTGACTAGTT[G/T]GTTTATACACACTTT | 51133 |
rs189606022 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566404 | TTCAAGTCGAATCTA[G/T]ATAGAGCATATCACA | 51133 |
rs189643528 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573977 | TTGGAAGATAGATAA[C/T]TTACTTTTAGTGGTC | 51133 |
rs189645306 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615314 | AAAATTTTAAATAAA[A/G]GAGTAGTTTTAAGAA | 51133 |
rs189661596 | snp | A/G/T | 1.6593e-05 | 0.00288031 | missense | KCTD3 | GRCh38.p7 | 1:215579072 | TAAATTCTACAGAAG[A/G/T]TGAAGCCCGGGGAAA | 51133 |
rs189669625 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215618800 | ATAACATGTTTGCTT[G/T]CTTTCTTTCTGTCTT | 51133 |
rs189725764 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600434 | AGCTTCACTTCCTCT[C/G]TGAACCTTCCTTGAT | 51133 |
rs189898846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215593511 | GTACAGTTCTGAACA[A/G]AAAGAGAATACCTAG | 51133 |
rs189962848 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581269 | AATAAACAAATTTTT[A/T]AAAAAAGTGTTTTGT | 51133 |
rs190040982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612427 | TTCTATTTTAGACCT[A/G]TTTCCATCTACTTTA | 51133 |
rs190058244 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571183 | GTTATAAGCTGTCCT[C/T]ATTTGGAATGAATTT | 51133 |
rs190071311 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591024 | CTTCTAGCTTTATTT[A/G]TAATTTTAGGGCAGG | 51133 |
rs190124862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584505 | ATGGGTTTATCATTG[C/G]CTGCAAATACCTGTA | 51133 |
rs190276297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585508 | GTTTGCTTTTTGCAG[C/T]GAATGTCAGGTAGTG | 51133 |
rs190347174 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604463 | TTAAAGATTTCTTTG[A/G]GCTGGTCGTGGTGGC | 51133 |
rs190388397 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616367 | TAATTTGTCACCTAT[G/T]TATGATTTAAAAAAA | 51133 |
rs190440708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609883 | TGAAGATATACCTGG[C/T]TTCTGGAGAAAGAAC | 51133 |
rs190479700 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567023 | TTTTACTACCTCTAG[G/T]ATTAGTTTTTCCTTT | 51133 |
rs190599980 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215575677 | AATATCAGTTTAATA[A/G]TAACTATTCAGAGGA | 51133 |
rs190610138 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596267 | GAGGCTGGTGGGTAG[G/T]GTGAAGAATTATTAG | 51133 |
rs190726944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587707 | CACAGATATGTAGTT[C/G]GAAAAAACTTTTTTC | 51133 |
rs190871742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574950 | TTGGTATAAATTTCC[A/G]TAAAAAGTTATCAAT | 51133 |
rs190879083 | snp | A/G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588857 | ATTGACTCTCTGCCA[A/G/T]ATCTTTAGATTGAAG | 51133 |
rs190925629 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570376 | AGAATTGTTAGTATT[A/C]GTTATTTACAAAAAG | 51133 |
rs190965015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580343 | TAATGTGAGCTCCCT[G/T]ATGGTCTATCTCTAA | 51133 |
rs191006974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215606177 | ACTTTTGTGTTTGTT[C/G]TTTTTATTTGAAATG | 51133 |
rs191137859 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570140 | AAGTTCAGGAACTGC[A/T]GTGGCATAGAATTGA | 51133 |
rs191143787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215600266 | AGAAATTAGGATTAT[A/G]TACAGGAAGAGCTTA | 51133 |
rs191150071 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611234 | GGGTGCAACTCAGTA[C/G]TACATTTTATACTGT | 51133 |
rs191150903 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215603666 | TAGACATAATAAGGA[A/G]TATTGCTTTTGGAAT | 51133 |
rs191155114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583412 | TTAGCATGATAATGC[A/G]TTATAATTAGCGTAT | 51133 |
rs191230496 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576707 | CAAGTAGCTGGGACT[A/G]CAGGCACCCGCCACC | 51133 |
rs191413217 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580856 | GATGTATTTTTTTTT[A/T]AAAAATCTGAATTTA | 51133 |
rs191431318 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215596952 | ACAGGGAGTAGAGAC[A/T]TTTCTTTCTCTGTGA | 51133 |
rs191682624 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215566021 | CAAAAGATTGGACAC[C/T]CTGGTTTAGATTCCT | 51133 |
rs191705696 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586909 | AACCTGGCTGCTCTA[C/T]GAAAATATTGCTTTT | 51133 |
rs191843278 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577420 | TAATCTCTCCTTTAG[A/T]GACCCAATTCATATA | 51133 |
rs191865847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608610 | AACAATGTAGTATGT[C/G]TCCTTTGATATTCTC | 51133 |
rs191965347 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594573 | TTTTCAACCCCCTTT[A/C]CATACCCTTTTTACC | 51133 |
rs191997481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612173 | GAACACAGTGAACTT[C/T]TTTTCATGGCCAAAC | 51133 |
rs192012237 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597461 | CATAGGTTATACATG[C/T]TTCATTCTCATATCA | 51133 |
rs192016734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578619 | TGTCAAATAAAAAAT[A/G]TTTGAAAGTATGGGG | 51133 |
rs192019343 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617125 | GTTCTGAAGGGTGGC[A/G]TGCCCAGGGAGGGCA | 51133 |
rs192216690 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591868 | ATTAGTCCGTTTTCA[C/G]ACTGCTGATAAAGAC | 51133 |
rs192241806 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215585912 | GATATCCTGCACCCT[A/G]TCCTTTTTTATATAA | 51133 |
rs192246985 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616171 | ACTTTGCTTCTGAGG[A/G]TATTTTCTGAGACCC | 51133 |
rs192341914 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215589840 | TGTTTATCCATTCAC[A/C]CGTTGATAGACATTT | 51133 |
rs192470125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215597237 | AGAAAAGTAAAAAAA[A/G]AAAAAAAGAAATGTT | 51133 |
rs192477955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616805 | GATATTGTGAAATAC[A/G]TATTTGGTCTTTGTC | 51133 |
rs192490313 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577370 | TCTATCGTTTGCCTT[C/G]TAGACAATTTATTTG | 51133 |
rs192531420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572538 | ATCCAGTGCTATTTA[A/G]TAGCCCACTTAGAAG | 51133 |
rs192534722 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602540 | TTTTCACTTAAAAAT[A/T]AGGAGCTTTTTAAAA | 51133 |
rs192576491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215613150 | AAGTTACAGGGAAAA[A/G]GTTTTTTGCATGTCA | 51133 |
rs192630682 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215572177 | AGAAGAATCAAGTCT[C/G]CGTTTTGTACAGAAC | 51133 |
rs192665352 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603368 | CCAGTAAAGCTAAGA[C/T]GTTCTCTATCCATGA | 51133 |
rs192687460 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KCTD3 | GRCh38.p7 | 1:215592373 | TTGTCCATTTTTTTT[G/T]TTGTTGTTACTGCTG | 51133 |
rs192800766 | snp | A/C | | | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620785 | ATACAATAATCATAT[A/C]TCTTTTGACATTTTG | 51133 |
rs192843798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586824 | TAATGTGGGAGGAAT[A/G]ATCTGATAATGAAGG | 51133 |
rs192879086 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582851 | CCAGGCGTGAGCCAC[G/T]GTGCCTGGCCTTGTT | 51133 |
rs193008966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215598355 | ACATATTCAAATTAG[A/G]AGTGAATTGAAGCAC | 51133 |
rs193055062 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607299 | ATTTTTTATTAAAGC[A/G]TGCCAAAAAAAGTAG | 51133 |
rs193058563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215609848 | TTCTGTGGTATGAAG[A/G]TATACCTGGTTCTGT | 51133 |
rs193099398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215582303 | TCTCATTTCCTTAAG[A/T]CATATGTCTATTCTC | 51133 |
rs193238159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587286 | AGGCACATGCCACCA[C/T]GTCCAGCTAATTTTT | 51133 |
rs199535715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577967 | TTTTCTGTTTGCATG[C/T]ACTCTTGACAAGTTT | 51133 |
rs199544794 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577336 | AAAGCAACTAATGCC[A/G]TAAAAGAATGGTTTC | 51133 |
rs199617836 | in-del | -/TT | 0.0287284 | 0.116357 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616448 | ATAATTCTTTCAAAC[-/TT]TTTATATTGGCGAAA | 51133 |
rs199663192 | snp | A/G | 4.98591e-05 | 0.0049927 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215611910 | TGTAAGACTCTCATC[A/G]ACTGGAAAAAGGTAA | 51133 |
rs199687655 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215580847 | AGAATCCCAGATGTA[-/T]TTTTTTTTTAAAAAT | 51133 |
rs199733337 | in-del | -/T | 0.00875954 | 0.0655975 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608687 | TACACCATACATACG[-/T]GTGCACATGGGCACT | 51133 |
rs199892787 | in-del | -/AT | 0.0178098 | 0.0926698 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608716 | CTCACACATCCACAC[-/AT]GTGTGCATACACATA | 51133 |
rs200014391 | snp | A/G | 4.948e-05 | 0.00497369 | missense | KCTD3 | GRCh38.p7 | 1:215619254 | AGTCCAGCAACTTCC[A/G]TAGTTCAGCATAGCC | 51133 |
rs200120296 | snp | G/T | 1.71879e-05 | 0.00293149 | missense | KCTD3 | GRCh38.p7 | 1:215620613 | GGTCAGGAGTACAGC[G/T]TGTGAAAACTCACCA | 51133 |
rs200161521 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215572257 | ATAAACATTTACTGG[A/G]TGTGTGCTAGGTGCT | 51133 |
rs200168547 | snp | A/T | | | splice-acceptor-variant | KCTD3 | GRCh38.p7 | 1:215586493 | CTGTTCTTCCTTAAC[A/T]GAATCAAAGAATCTT | 51133 |
rs200258521 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596260 | AAGCAGAGAGGCTGG[G/T]GGGTAGGGTGAAGAA | 51133 |
rs200281298 | in-del | -/AGTTCTA | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602774 | ATCTGTAATGAAAGG[-/AGTTCTA]AGTTCTAAGAAACAA | 51133 |
rs200388773 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598714 | AAAAAAAATTTTTAA[A/T]TTTATTTAATGGTTA | 51133 |
rs200399910 | snp | A/G | 0.00355684 | 0.0420211 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604096 | TTTTATTATCGTTCC[A/G]TAATGTATCACCTGT | 51133 |
rs200443021 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215603235 | TGTAGTGGCAGGGGG[A/G]TTTTAAGGCATGAAA | 51133 |
rs200538044 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616532 | TTGGGAGGCTGAGGT[-/G]GGCGGATCACCTGAG | 51133 |
rs200579571 | snp | A/G | 1.65614e-05 | 0.00287757 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580024 | AATTAATAATGCTTT[A/G]CTTTTACAGGTGGCA | 51133 |
rs200612833 | snp | A/C | 0.000270929 | 0.0116358 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601856 | ATCTGATAATACTCT[A/C]ACTACATCAGGTTCA | 51133 |
rs200685184 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215570640 | CAATCTTATCAGATT[C/T]TTATAGGAATTTGAA | 51133 |
rs200797797 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215599893 | GCTGCTCTTTCATTG[-/A]AAAAAAAAAAAAAAA | 51133 |
rs200835375 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608687 | TACACCATACATACG[G/T]GTGCACATGGGCACT | 51133 |
rs200851957 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601981 | GTCACTTAAAATGCT[C/G]CTGCTTAATGTAATT | 51133 |
rs200859043 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598707 | GTCATTGAAAAAAAA[A/T]TTTTAATTTTATTTA | 51133 |
rs200921370 | snp | C/T | 0.000315083 | 0.0125476 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573760 | TCATGTTCTCACTTA[C/T]AATACCAGATGATTT | 51133 |
rs200976075 | snp | C/T | 0.00174882 | 0.0295187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608002 | GTATTCTTTTGTGTT[C/T]TCTTTCTCTGCTAGT | 51133 |
rs201000947 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215582836 | CAAAGTGCTGGGATT[A/C]CAGGCGTGAGCCACT | 51133 |
rs201062587 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619220 | TTTGAGCACATCTCG[C/T]TGTGCTACTCCTAAC | 51133 |
rs201188483 | snp | A/G | 0.00199804 | 0.031544 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620210 | TTTGAACAGAAATGT[A/G]GAAAGAGCTGTCCCT | 51133 |
rs201239948 | snp | A/G | 0.00416293 | 0.0454328 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567780 | CCAGGTGAGTCGGCG[A/G]GTAGCGGGCTTGCAG | 51133 |
rs201370604 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599917 | AAAAAAAAAGAATGT[A/T]TCCAAAGGGAGAAGA | 51133 |
rs201498407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579662 | CGCCACCATGCCAGA[C/T]TAATTTTTTGTATTT | 51133 |
rs201590334 | snp | C/T | 0.000141493 | 0.0084099 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579172 | ATAGAAAAAGAAAAA[C/T]ACGTATGTTTTTAGT | 51133 |
rs201828602 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566459 | ATTTTTTATTTTTTT[G/T]GTAAAAATTATGACA | 51133 |
rs201839094 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598712 | TGAAAAAAAATTTTT[A/T]ATTTTATTTAATGGT | 51133 |
rs201940638 | snp | A/T | 0.000460574 | 0.0151682 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604109 | CCATAATGTATCACC[A/T]GTCAACTCTTGACTT | 51133 |
rs201946355 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215594108 | CAAGTGATCCACCCG[C/T]CCTGGCCTCCCAAAG | 51133 |
rs202013188 | snp | A/C/T | 8.36469e-05 | 0.00646663 | missense | KCTD3 | GRCh38.p7 | 1:215620586 | CCTCGGCATAAAAAA[A/C/T]GTGATTCTTCAGGTC | 51133 |
rs202044566 | snp | C/G/T | 3.29833e-05 | 0.00406088 | missense | KCTD3 | GRCh38.p7 | 1:215620499 | TATCTGGCGTCATCA[C/G/T]CAAGTACTTCCGATG | 51133 |
rs202078864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586715 | GTTTATGTTGCAATT[C/T]GATGATATTAATATT | 51133 |
rs202083972 | snp | A/G/T | 0.000181565 | 0.00952638 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215620646 | ATGAATAGTTGTTTC[A/G/T]TTACATTTAGATGAA | 51133 |
rs202110919 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577155 | TTTTTTTCTATTTTA[-/T]TTGTTCAACAAATAT | 51133 |
rs202164409 | snp | A/G | 0.000116124 | 0.00761895 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215604289 | CATGCTATCAGAGAA[A/G]CATCTTGTATCAGGT | 51133 |
rs267598368 | snp | C/T | | | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620162 | AAGAAGGACTGAGAG[C/T]TTTCACAGTTATAGG | 51133 |
rs367568021 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | KCTD3, LOC105372919 | GRCh38.p7 | 1:215566295 | AATATCTAAACCACC[A/G]GGTATATGATAAACA | 51133 |
rs367570777 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606949 | GCTTAGTAGTGAAAT[C/G]AGGAAATGATTTCCC | 51133 |
rs367580174 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575049 | ATGAGGTCAAGAGAT[C/T]AAGACCATCCTGCCC | 51133 |
rs367837334 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215616519 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGTGGG | 51133 |
rs367841363 | snp | C/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568475 | CTGTCTGTTCTCTTT[C/T]TGGCCTTCCGCCCCC | 51133 |
rs367845820 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581290 | AGTGTTTTGTGGATT[C/T]GTAATTTTAATTATG | 51133 |
rs367846739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611160 | GGCTATTTATCTGTC[C/T]TGCCAAATACAATAA | 51133 |
rs367892719 | snp | A/G | 3.31901e-05 | 0.00407356 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586689 | GAAGTGAAATTGGTA[A/G]GAAGAATCTTGTTTA | 51133 |
rs367935326 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215612894 | CTCAGATTTTGCTTC[A/T]ACATTCCTCTGCATT | 51133 |
rs367959474 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215586417 | TTGTTGTTGTTTTTT[-/G]TTTTTGGTGCATTGA | 51133 |
rs368035629 | snp | C/T | 3.29522e-05 | 0.00405894 | missense, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577689 | GTGAGTATTAATGTT[C/T]TCAGGCATGAAGCAG | 51133 |
rs368081174 | snp | G/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568147 | CTGGCTTTGTGGTTT[G/T]GATGTTGGAGATGAA | 51133 |
rs368089194 | snp | C/T | 1.70449e-05 | 0.00291928 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604341 | TAAGGAACTTGGCTC[C/T]GTGTGTTATTTTCAT | 51133 |
rs368121551 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588127 | AGGCTTACTTTGTTT[A/G]TTTTTTGAGGATAGT | 51133 |
rs368217640 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567315 | CCTCATTCTAGGCGG[C/T]AGTGGCGGGCGAAGC | 51133 |
rs368244156 | snp | A/C | 2.10051e-05 | 0.0032407 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611794 | AATAAAATTTTAATT[A/C]ATTTTTTGACATTTT | 51133 |
rs368250029 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215620354 | TAGTGGATTGGAAGT[A/G]CATAAAATAGCTGAA | 51133 |
rs368255087 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618614 | CTCAGGTTCTTTTAT[A/C]TTTTATGAAAATCAA | 51133 |
rs368257204 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576752 | TTTTTGTATTTTTAG[G/T]AGAGATGGGGTTTCA | 51133 |
rs368372353 | snp | A/T | 0.000168265 | 0.00917084 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604319 | TAAAATGATTTCATT[A/T]TACTGGTAAGGAACT | 51133 |
rs368679009 | snp | C/G/T | 3.29474e-05 | 0.00405867 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215578038 | AGAATTGGAGCGTTC[C/G/T]TCTTGTGGCAGTGTC | 51133 |
rs368702528 | snp | A/G | 0.00152089 | 0.0275342 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586474 | CTGAGTCTACCTTAT[A/G]TGCCTGTTCTTCCTT | 51133 |
rs368718120 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581669 | ATTTTCCAGTCTTTG[C/T]GTTTGCATTGATCAC | 51133 |
rs368752457 | snp | A/G | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215579020 | CCTAGTCGTAAAATA[A/G]ACAACACAGTCAGAT | 51133 |
rs368806320 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567301 | TCCTCCTCCTCCTCC[-/C]TCATTCTAGGCGGCA | 51133 |
rs368978996 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570644 | CTTATCAGATTGTTA[C/T]AGGAATTTGAAGTAA | 51133 |
rs368987741 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586723 | TGCAATTTGATGATA[C/T]TAATATTTTGAAGTT | 51133 |
rs369092198 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613394 | CTTATAGATGCTGGA[C/T]ATTAGACCTTTGTCA | 51133 |
rs369232802 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583411 | TTTAGCATGATAATG[C/T]ATTATAATTAGCGTA | 51133 |
rs369353077 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584830 | TTACATATTGCTGTA[A/G]GTTAAGAATACTCAC | 51133 |
rs369363133 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590340 | GATTTGTGTTTCACA[A/G]CCAAGGAAATCTTAT | 51133 |
rs369363237 | snp | C/G | 9.92507e-05 | 0.00704383 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619147 | ATGACTATTTGTTCT[C/G]CTAAGATGTAGGTGG | 51133 |
rs369440672 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215607303 | TTATTAAAGCATGCC[-/A]AAAAAAAGTAGTTTT | 51133 |
rs369459873 | in-del | -/T | 0.0667028 | 0.170006 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612404 | ACAACATAGCACACA[-/T]TTTTTTTTTCTATTT | 51133 |
rs369505326 | snp | C/T | 0.000312533 | 0.0124967 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602044 | AGTTTTAAATAGATA[C/T]GCTATTTATTTTAAT | 51133 |
rs369511517 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599552 | TTTATATTTGTGACC[A/C]CATGACTGAACCATG | 51133 |
rs369520649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616482 | TAAAAACTTCCAGGC[C/T]GGGTGCGGTGGCTCA | 51133 |
rs369570683 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215569726 | TCAGCCTGGCACTGT[G/T]ACATTTTATCTTGTG | 51133 |
rs369635348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215617275 | ATTAGTTGAACCTAA[A/G]GAGGAGGCTGTGGGA | 51133 |
rs369697592 | snp | G/T | 0.000153988 | 0.00877328 | splice-donor-variant | KCTD3 | GRCh38.p7 | 1:215619071 | AAAGTGAAGATAAGG[G/T]TAGGTTCTCATACAG | 51133 |
rs369772840 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617314 | TTACAGTCAGTCAGT[C/T]AGAAGCACAGGCAAA | 51133 |
rs369890988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591482 | CCTGCCTCAGCCTCT[C/T]GAGTAGCTGGGACTA | 51133 |
rs369912970 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600182 | CCTGACCTCAGGATA[C/G]GGCATGATGATTGAG | 51133 |
rs369916350 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215584567 | TTCATGATAACTTGG[G/T]GCTTTTGGGCCTGTC | 51133 |
rs369917312 | snp | A/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569624 | TTTTTGAGACAGAGT[A/C]TCGCTCTGTCATCCA | 51133 |
rs369942900 | snp | A/C/G | 6.62508e-05 | 0.00575514 | missense | KCTD3 | GRCh38.p7 | 1:215601885 | CAAGATGTTGTTCCT[A/C/G]TAACTAGTTATGACA | 51133 |
rs369948550 | snp | A/G | 8.92642e-05 | 0.00668013 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579175 | GAAAAAGAAAAATAC[A/G]TATGTTTTTAGTGCT | 51133 |
rs370026945 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618393 | ATTGTATTTTTTTTT[-/T]GTCTATTTTTTTGAC | 51133 |
rs370087933 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215615648 | AAAAGAAATCTGCAT[-/A]GGGGGAAAAAAGTTC | 51133 |
rs370147635 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617826 | TTTAATATATATTAA[A/T]TATATATTACATATA | 51133 |
rs370171990 | snp | A/C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577309 | TATAGAAATAATTGC[A/C/G]ATAAAAAGTTAAAAG | 51133 |
rs370200562 | snp | G/T | 0.000154431 | 0.00878587 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586466 | CATTGCTGCTGAGTC[G/T]ACCTTATGTGCCTGT | 51133 |
rs370278630 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595258 | TTTGTAGTAATGAGA[A/G]TATAAATTAGTCACC | 51133 |
rs370298874 | in-del | -/T | 0.0182127 | 0.093673 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621582 | AACGTTTTTGTACAA[-/T]TTTTTTTCATTTAAT | 51133 |
rs370327389 | snp | A/C/T | 3.29616e-05 | 0.00405954 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577732 | TCACTCCATTAGGTA[A/C/T]GTGCTCTTTTAATAT | 51133 |
rs370333076 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615492 | AGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 51133 |
rs370357390 | snp | A/T | 0.000724321 | 0.0190167 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620036 | AAATCTGAACTGTCA[A/T]TTTTAAAAACTGTAT | 51133 |
rs370415509 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569963 | AAACAACATCCGACT[C/G]CATATTCTAAGAATA | 51133 |
rs370474264 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215610873 | CATTTACGGTGGCAC[A/G]TAGTAAGTACAGTGT | 51133 |
rs370480597 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581224 | GTACTCCAACCTGCG[C/G]AACAGAGCAAGACTC | 51133 |
rs370509594 | snp | A/G | 0.000263678 | 0.0114791 | missense | KCTD3 | GRCh38.p7 | 1:215579927 | TTCCTGTGGATCCAC[A/G]AAAGGTGCTAATAGT | 51133 |
rs370535368 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614493 | GTTGTCTGCTTTCTT[C/T]GAGCAGTGTTTTTGT | 51133 |
rs370535866 | snp | C/T | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622031 | TCTTTATGACAGTTA[C/T]GTGAAAGTTGGGTGG | 51133 |
rs370585840 | snp | C/G | 3.3184e-05 | 0.00407319 | missense | KCTD3 | GRCh38.p7 | 1:215620424 | AATGAAAATAAAATA[C/G]AGTTTAGGAAGAAAG | 51133 |
rs370629984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587409 | GCTGGAATTACAGGC[A/G]TGAGCCACCATGCCC | 51133 |
rs370742709 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587427 | AGCCACCATGCCCGG[C/T]CTTTCTGTAGGTTAT | 51133 |
rs370765684 | snp | A/C | 1.64798e-05 | 0.00287047 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577662 | TTACATCATTTGTTT[A/C]TTTGTAGGGGAGTGA | 51133 |
rs370783791 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571801 | CACGCCTGGCTAATT[A/T]TTCGTAGTTTTAGTA | 51133 |
rs371114155 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215622245 | AGTGGTTTATGTCTG[G/T]CTACTCTGACACTAA | 51133 |
rs371136563 | snp | A/G | 1.6554e-05 | 0.00287693 | missense | KCTD3 | GRCh38.p7 | 1:215620268 | GCTGAAGTGAAAGGG[A/G]CAACAGGGGAATGTA | 51133 |
rs371151534 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596616 | TTAGTTAGGTGTTGG[C/T]GGAAGAAAGCTAGGT | 51133 |
rs371164388 | snp | A/C/G | 1.6638e-05 | 0.00288422 | missense | KCTD3 | GRCh38.p7 | 1:215579053 | GCTGATTCTAGGAAT[A/C/G]GTCTAAATTCTACAG | 51133 |
rs371276905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215599310 | AGATGTTGGTAAATA[C/T]GATGGTAAATTTAGA | 51133 |
rs371282812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568480 | TGTTCTCTTTCTGGC[C/T]TTCCGCCCCCCCCCC | 51133 |
rs371322135 | snp | C/T | 1.65965e-05 | 0.00288062 | intron-variant | KCTD3 | GRCh38.p7 | 1:215574132 | CTGTGAGTATAATAA[C/T]AATTGATACATATTC | 51133 |
rs371337308 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581312 | TTAATTATGAAATAG[C/T]ATGGAAATTGTTTTT | 51133 |
rs371409133 | snp | C/T | 3.4064e-05 | 0.00412684 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601853 | AACATCTGATAATAC[C/T]CTCACTACATCAGGT | 51133 |
rs371501116 | snp | A/G/T | 1.691e-05 | 0.0029077 | missense | KCTD3 | GRCh38.p7 | 1:215620598 | AAAAGTGATTCTTCA[A/G/T]GTCAGGAGTACAGCT | 51133 |
rs371508066 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570989 | AAAAAATTGGTGGGG[A/T]TGAGGGTCTAATTCC | 51133 |
rs371548997 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574735 | TCTGTGATGTCTCTT[C/T]GATTTTTGATGTGCT | 51133 |
rs371569874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616488 | CTTCCAGGCCGGGTG[C/T]GGTGGCTCACACCTG | 51133 |
rs371575827 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596934 | CTAGAAAGGTTTGAC[C/G]CAACAGGGAGTAGAG | 51133 |
rs371623164 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567075 | GGGTCATAAAGATCC[A/G]TAGATCGTTTGCCCA | 51133 |
rs371692182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578669 | TTAAATTATTACATA[A/G]TACCTAACACATAAT | 51133 |
rs371729645 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215611328 | GTGTTTTTTTAATTT[A/G]CATCTTTAAAAAGAA | 51133 |
rs371796924 | snp | A/G | 3.6135e-05 | 0.00425043 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607976 | TAAAATGAGTTTTTA[A/G]AAGTAATTTTGTATT | 51133 |
rs371875871 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215604354 | TCTGTGTGTTATTTT[C/T]ATTAAAAGAATGAAA | 51133 |
rs371879570 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567411 | GTGGCAGCGGAGCAC[G/T]GAGAAGAGGCCCGGG | 51133 |
rs371959356 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215590679 | TTTAGCTCTAGTATT[A/G]CTTTTTGATTCCATT | 51133 |
rs371972516 | snp | A/C/T | 6.98147e-05 | 0.00590791 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578995 | TTTTCTTCTTCTCTT[A/C/T]ATAGGTATTCCTAGT | 51133 |
rs372012064 | snp | C/T | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215578076 | ATGGTTACTTGCCCC[C/T]ACCAGGTATTTTCAC | 51133 |
rs372043006 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215591601 | ACCTCGTAATCCGCC[C/T]GCCTCAGCCTCCGAA | 51133 |
rs372159813 | snp | A/G | 3.29853e-05 | 0.00406098 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586666 | GAGTGTTCAGGATGG[A/G]GGAAGTGGAAGTGAA | 51133 |
rs372206085 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215612355 | AATAAAAATGATATT[A/T]ATAACACTAATTTGC | 51133 |
rs372215144 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613161 | AAAAAGTTTTTTGCA[C/T]GTCAAACAAATGAAA | 51133 |
rs372233368 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601996 | CCTGCTTAATGTAAT[G/T]TTTTAAATGAGAACA | 51133 |
rs372331747 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577970 | TCTGTTTGCATGTAC[C/T]CTTGACAAGTTTGCT | 51133 |
rs372344342 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215615847 | GCTTAGGTTAGAAGA[A/G]GCAGGGACAGCCATG | 51133 |
rs372352951 | snp | C/T | 1.65121e-05 | 0.00287329 | missense | KCTD3 | GRCh38.p7 | 1:215608125 | TCAAGATACTATCCC[C/T]GGAGGAGACAGAAAG | 51133 |
rs372419654 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606976 | TCCCGTGAAACTAAA[C/T]AGCCTAGAACAAAAT | 51133 |
rs372677593 | snp | C/T | 1.65021e-05 | 0.00287241 | missense | KCTD3 | GRCh38.p7 | 1:215586530 | GGCAGCAAGTGTTTA[C/T]GAGCCCATATTTGGA | 51133 |
rs372740101 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215592375 | GTCCATTTTTTTTTT[-/T]GTTGTTACTGCTGTT | 51133 |
rs372777136 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KCTD3 | GRCh38.p7 | 1:215588819 | CTGTTTGCAAGGCAA[A/G]AATACAATTCTACAG | 51133 |
rs372841584 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215573305 | AGATGGACGGATCTT[C/G]AATTATTGGACATGA | 51133 |
rs372915139 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575313 | TTAAGCAATTTGTTT[C/T]CCTCTTATGTATTCT | 51133 |
rs372952944 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617597 | TATTTTGAGGTGAAA[A/G]CATTAGAGAAATTGT | 51133 |
rs372954077 | snp | C/G | 1.91316e-05 | 0.0030928 | intron-variant | KCTD3 | GRCh38.p7 | 1:215620018 | CTGAGAAATCACAGA[C/G]TGAAATCTGAACTGT | 51133 |
rs372979043 | snp | A/C | 1.74081e-05 | 0.00295021 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602046 | TTTTAAATAGATATG[A/C]TATTTATTTTAATGC | 51133 |
rs372993960 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215601036 | TCTGCCTCCCAGGTT[C/T]GAGCAATTCTCCTGC | 51133 |
rs373023035 | snp | C/G/T | 0.000160669 | 0.00896174 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576005 | TTTTTAAAGTAAATT[C/G/T]TTACTGATAAATATG | 51133 |
rs373116681 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613415 | ACCTTTGTCAGATGC[G/T]TAGTTTGCAGATATT | 51133 |
rs373163179 | snp | C/T | 5.34345e-05 | 0.0051686 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579864 | GCTGTAATTTGCCAA[C/T]CCCCGGTTTAGAATG | 51133 |
rs373165570 | snp | C/G | 1.65789e-05 | 0.0028791 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619123 | AAGCTTTTCACTTAA[C/G]TGATTTTAATGACTA | 51133 |
rs373166644 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215618413 | TTTGTCTATTTTTTT[-/T]GACCTTGCGTTTGCC | 51133 |
rs373169812 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617337 | CAGGCAAAATAACCT[C/G]AGGCTTGTGATCAGC | 51133 |
rs373176979 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591938 | ATTGGACTTACAGTT[C/G]CACATGGCTGGGGAG | 51133 |
rs373232244 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215574781 | AAAATTTATAAAGCT[-/G]TAGAAGAATCTCATT | 51133 |
rs373285973 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215600289 | AGAGCTTAGAGGAAT[G/T]ATTATTTCCAAGTTT | 51133 |
rs373290742 | snp | A/T | 0.000155988 | 0.00883005 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573776 | AATACCAGATGATTT[A/T]TAATTGCAGATTTAG | 51133 |
rs373298761 | snp | A/G | 0.000247965 | 0.011132 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619150 | ACTATTTGTTCTCCT[A/G]AGATGTAGGTGGTCC | 51133 |
rs373299338 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569695 | CCGCCTCCCAGGTTC[A/G]CGCCATTCTCCTGTC | 51133 |
rs373310189 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570014 | TCCTACACTCGTGCA[A/G]CATTTTAGAGCTAGA | 51133 |
rs373310644 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613843 | GGGTTCTGCATCCTG[A/T]TGCTTTGGTCTATGT | 51133 |
rs373311674 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215584736 | ATCTGAAAGCATGCT[A/C]TTCCAGTCAAAGTCT | 51133 |
rs373333364 | in-del | -/T | 0.105569 | 0.204058 | intron-variant | KCTD3 | GRCh38.p7 | 1:215573913 | TGTTTGTCAGTTAAA[-/T]TTTTTTTTAATAAAA | 51133 |
rs373482661 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569850 | GAACAGTTTACAAGA[C/G]ATGAAATTGTTAGTG | 51133 |
rs373485512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215576728 | ACCCGCCACCACACC[C/T]GGCTAATTTTTTTGT | 51133 |
rs373510305 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608685 | TATACACCATACATA[C/T]GTGTGCACATGGGCA | 51133 |
rs373747139 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215587989 | ATCCCTGCTGACTAC[A/G]TGTGAGGGAGTTGTC | 51133 |
rs373803481 | in-del | -/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215617587 | GTATATTGATTATTT[-/T]GAGGTGAAAACATTA | 51133 |
rs373830757 | snp | G/T | 1.6727e-05 | 0.00289193 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601978 | TCAGTCACTTAAAAT[G/T]CTCCTGCTTAATGTA | 51133 |
rs373921273 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565856 | ATGGGTCGCATGCAG[C/T]CCAGGAAAGCTTTGA | 51133 |
rs373965485 | snp | A/T | 8.24518e-05 | 0.00642021 | intron-variant | KCTD3 | GRCh38.p7 | 1:215580004 | GTGTGTTACAGGTAG[A/T]GTATAATTAATAATG | 51133 |
rs373990191 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215581237 | CGCAACAGAGCAAGA[C/T]TCTGTCTCAATAAAT | 51133 |
rs374046660 | snp | A/G | 1.66565e-05 | 0.00288583 | missense | KCTD3 | GRCh38.p7 | 1:215579048 | GATCTGCTGATTCTA[A/G]GAATGGTCTAAATTC | 51133 |
rs374128463 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586472 | TGCTGAGTCTACCTT[A/G]TGTGCCTGTTCTTCC | 51133 |
rs374142801 | in-del | -/AGT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215571469 | GTGAAATTAGTTAGT[-/AGT]CAACTTCTATGTGTT | 51133 |
rs374201216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571621 | ATGTGGGAAGAAGTG[A/G]AGATAAACTTTTTTT | 51133 |
rs374235399 | in-del | -/TTACTAAGACCATTACAT | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588361 | AAGGACATTCTTTAG[-/TTACTAAGACCATTACAT]TCTCTGCCACAGACT | 51133 |
rs374278894 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215593903 | TCTTGCTCTGTCACC[C/T]AGGCTGGAGTGCAGT | 51133 |
rs374358282 | in-del | -/A | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215575344 | GTGGTGCTTTAGTTT[-/A]AAAAAAAAAAATTGT | 51133 |
rs374406237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215614918 | GTAGTGTTCTCTGCA[C/T]AGTGAAGAAACTGCC | 51133 |
rs374524780 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621201 | TGATTTTAATTTAGT[C/T]GTGCGTCATTTTCTG | 51133 |
rs374541317 | snp | C/T | 8.23866e-05 | 0.00641767 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577712 | TGAAGCAGAATTTTA[C/T]GGGATCACTCCATTA | 51133 |
rs374568486 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KCTD3 | GRCh38.p7 | 1:215594169 | CCGGCCGATTATAAC[A/T]TTTTTAAGCTCAAGT | 51133 |
rs374649981 | snp | A/G | 1.65326e-05 | 0.00287507 | missense | KCTD3 | GRCh38.p7 | 1:215620226 | GAAAGAGCTGTCCCT[A/G]AAAATGGTAACTTGG | 51133 |
rs374676834 | snp | C/G | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568501 | CCCCCCCCCCCCCCC[C/G]CCCCTTCTGTGCCTG | 51133 |
rs374837051 | in-del | -/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614966 | TATCATAACATTCTC[-/G]TAACAATGTAGTATA | 51133 |
rs374970983 | snp | A/G/T | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215577666 | ATCATTTGTTTCTTT[A/G/T]TAGGGGAGTGAGTAT | 51133 |
rs375009609 | snp | C/T | 0.000606244 | 0.0173998 | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567813 | GGGATGCCTTGGCGG[C/T]CTCCTCCTTTGGTGT | 51133 |
rs375011529 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607997 | ATTTTGTATTCTTTT[C/G]TGTTCTCTTTCTCTG | 51133 |
rs375054033 | in-del | -/AA | 0.00542466 | 0.0517967 | intron-variant | KCTD3 | GRCh38.p7 | 1:215581005 | GTGGGTCACGCCTGT[-/AA]AATCCCAGCACTTTG | 51133 |
rs375096968 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215567493 | CACCGCAGGATTGAC[C/T]CGGGAAGGGGCAGAA | 51133 |
rs375097308 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215619132 | ACTTAAGTGATTTTA[A/G]TGACTATTTGTTCTC | 51133 |
rs375207862 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215589125 | TAAAATACTTAATTC[C/T]TTTTCTTCTTTTCTT | 51133 |
rs375223389 | snp | G/T | | | intron-variant, upstream-variant-2KB | KCTD3, LOC105372919 | GRCh38.p7 | 1:215568218 | CTTAGGGAAGAGTGC[G/T]GTGTTCTTTTCCGCG | 51133 |
rs375259128 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578508 | TCTGCAGAGATAAGT[C/T]AGTGTCACCTCAGCC | 51133 |
rs375402444 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602402 | CAAACATAATTTGAG[A/G]TGGAAAATTGGAACT | 51133 |
rs375410188 | snp | A/G | 0.000153988 | 0.00877328 | missense | KCTD3 | GRCh38.p7 | 1:215611833 | GATCAAGGACCTTTT[A/G]GAGAGCGAGACGATC | 51133 |
rs375463798 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604330 | CATTATACTGGTAAG[G/T]AACTTGGCTCTGTGT | 51133 |
rs375573504 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215598638 | AAAGCTGCTGTATTG[A/T]AGGAATAGGACAAAT | 51133 |
rs375582499 | snp | A/G | | | missense | KCTD3 | GRCh38.p7 | 1:215586611 | ATGGAGACAAAGACA[A/G]AATGGTTGCTGTTGC | 51133 |
rs375708623 | snp | A/G | 1.65952e-05 | 0.00288051 | missense | KCTD3 | GRCh38.p7 | 1:215620299 | ATATATCTGAGAGAA[A/G]GTCTCCTGGAGTAGA | 51133 |
rs375751467 | snp | A/G | 4.94907e-05 | 0.00497422 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215586531 | GCAGCAAGTGTTTAC[A/G]AGCCCATATTTGGAT | 51133 |
rs375833467 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215577977 | GCATGTACTCTTGAC[A/G]AGTTTGCTTTGAAAT | 51133 |
rs375849456 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576269 | AGAAGGGGTTTCACT[A/G]TGTTGCCCAGGCTGA | 51133 |
rs375881147 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570497 | GCCATTGAGGACTCC[C/T]GGACAAAGAGCTTTT | 51133 |
rs375981038 | snp | A/G | 3.40518e-05 | 0.00412611 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602076 | CTGTTTAAAATTTTT[A/G]TGTTTTAGATATGCA | 51133 |
rs376049494 | snp | A/G | 5.02542e-05 | 0.00501244 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604128 | AACTCTTGACTTTAT[A/G]TAGGTGTCAGTGGTA | 51133 |
rs376073710 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215588930 | GACTTTTCATCTAGC[A/T]GGCATTCAGCATTGT | 51133 |
rs376141537 | snp | C/T | 1.72934e-05 | 0.00294048 | intron-variant | KCTD3 | GRCh38.p7 | 1:215579878 | ACCCCCGGTTTAGAA[C/T]GTAAAATATTTCTTT | 51133 |
rs376240138 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215596048 | AAGCAGAGCACCTCA[A/G]CTAATGGCAGTGGTG | 51133 |
rs376247364 | snp | C/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565356 | TTTGTTAATGGTGTT[C/T]CAATTTATTCTTAAA | 51133 |
rs376278532 | snp | A/G | 1.65018e-05 | 0.00287239 | synonymous-codon | KCTD3 | GRCh38.p7 | 1:215619262 | AACTTCCGTAGTTCA[A/G]CATAGCCACTTACGA | 51133 |
rs376298361 | snp | A/G | 0.000121588 | 0.0077961 | intron-variant | KCTD3 | GRCh38.p7 | 1:215602037 | ACCTTTCAGTTTTAA[A/G]TAGATATGCTATTTA | 51133 |
rs376305384 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215595051 | CCTTTTTGTTTTGTT[C/T]TGTTTATTTTAAATC | 51133 |
rs376308177 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215614145 | TCACACTATTCTCCT[C/G]CGTCAGTTCCTGAGT | 51133 |
rs376336661 | snp | C/T | 0.00220135 | 0.0331033 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578102 | TTCACTTTATTAAAT[C/T]TTTTAAAAAATTCCT | 51133 |
rs376393927 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD3 | GRCh38.p7 | 1:215591075 | TTCTTATTTTTAAGA[C/T]GTTGCTTTTCTGGAA | 51133 |
rs376450817 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215578687 | CCTAACACATAATAC[C/T]TGTACCATAATTGTA | 51133 |
rs376456717 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215583353 | GTAACTTCCAGACAT[A/G/T]AGATGTCATTTGTAA | 51133 |
rs376463788 | snp | G/T | | | downstream-variant-500B | KCTD3 | GRCh38.p7 | 1:215621879 | TCATTTCTTTGCTTC[G/T]TCCCATAATTTAAAA | 51133 |
rs376505928 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KCTD3 | GRCh38.p7 | 1:215621376 | CCCAGAAGGGAAAGC[A/T]GTACCAGTTGCTAAC | 51133 |
rs376515310 | snp | C/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569714 | CATTCTCCTGTCTCA[C/G]CCTGGCACTGTGACA | 51133 |
rs376716578 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215606978 | CCGTGAAACTAAATA[A/G]CCTAGAACAAAATGT | 51133 |
rs376812729 | snp | A/G | 3.38816e-05 | 0.00411578 | intron-variant | KCTD3 | GRCh38.p7 | 1:215586722 | TTGCAATTTGATGAT[A/G]TTAATATTTTGAAGT | 51133 |
rs376836120 | in-del | -/C | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215583058 | TTATTGTGTAATACC[-/C]TAATTACTATAGAGA | 51133 |
rs376854435 | in-del | -/ATG | 0.0023933 | 0.0345097 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616317 | GTAATTCACTAAATT[-/ATG]ATCATCTTGATAAAT | 51133 |
rs376900676 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD3 | GRCh38.p7 | 1:215578716 | TAAAGAGTGGCTGGC[A/C]GACTGAATTAATTAC | 51133 |
rs376921002 | snp | C/T | 6.8712e-05 | 0.005861 | intron-variant | KCTD3 | GRCh38.p7 | 1:215604100 | ATTATCGTTCCATAA[C/T]GTATCACCTGTCAAC | 51133 |
rs377002113 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215616189 | TTTTCTGAGACCCAA[A/G]TTTTCATATGCATAC | 51133 |
rs377017503 | snp | C/T | 0.000465891 | 0.0152554 | intron-variant | KCTD3 | GRCh38.p7 | 1:215611793 | AAATAAAATTTTAAT[C/T]AATTTTTTGACATTT | 51133 |
rs377138141 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD3 | GRCh38.p7 | 1:215601443 | GTTGCTTTGTTTACT[A/G]GTTCTGATTCTGTCA | 51133 |
rs377213085 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215613852 | ATCCTGTTGCTTTGG[C/T]CTATGTGTTTGTTTT | 51133 |
rs377327988 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215602975 | GGGTTTAGTAAACCA[C/T]GGATTTCTAGCCAAG | 51133 |
rs377347322 | snp | C/T | 3.31175e-05 | 0.00406911 | synonymous-codon, utr-variant-5-prime | KCTD3 | GRCh38.p7 | 1:215573837 | AGATTCTTTTTTTTC[C/T]AGGTATGTCTTATAA | 51133 |
rs377352478 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215570639 | CCAATCTTATCAGAT[G/T]GTTATAGGAATTTGA | 51133 |
rs377409545 | snp | A/G | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215576770 | AGATGGGGTTTCACC[A/G]TTTTAGTCATGATGG | 51133 |
rs377417146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215587419 | CAGGCGTGAGCCACC[A/G]TGCCCGGCCTTTCTG | 51133 |
rs377466591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD3 | GRCh38.p7 | 1:215608354 | TCACAAAATTATTTT[A/T]TTGCAGCGTTTTTCC | 51133 |
rs377475272 | snp | C/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215608897 | TATATAATCCCAGTT[C/T]TCTGCATGATTCTAG | 51133 |
rs377521624 | snp | G/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215569905 | AGAAAATTGTTAAGA[G/T]AAAATGGCTTATAAA | 51133 |
rs377545052 | snp | A/T | | | intron-variant | KCTD3 | GRCh38.p7 | 1:215577788 | ATGAAAGTTGCCCTA[A/T]ATGAAATGTGTTTAT | 51133 |
rs377576867 | snp | A/T | | | upstream-variant-2KB | KCTD3 | GRCh38.p7 | 1:215565896 | AACACAAATTCATAA[A/T]CTTTCTTTCTTTCTT | 51133 |
rs377580044 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD3 | GRCh38.p7 | 1:215607051 | TTGTTATATAAGAAT[A/G]GAAAGTACACAGATG | 51133 |
rs377609197 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD3 | GRCh38.p7 | 1:215571891 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 51133 |