SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs710183 | snp | A/C | 0.0577344 | 0.159793 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054720 | CATCCTCCGgccagg[A/C]actgagctccatgct | 79734 |
rs710184 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057219 | GAGATGGTGCCTGGT[A/G]AATGCCTGGTGAGGA | 79734 |
rs710185 | snp | C/T | 0.231937 | 0.249347 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057412 | GGTCCCACCCAAGCA[C/T]GTGTACCGCGTGCTG | 79734 |
rs855792 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059645 | CGGCTGCACCCTGGG[A/G]ATGCTCTCATTTCAC | 79734 |
rs855793 | snp | A/G | 0.273856 | 0.248859 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053568 | GCCTGTCAACACTGC[A/G]TTCCTGTCACCCCAG | 79734 |
rs855794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052820 | GGTGAGAGGATGTCT[A/G]AGTGGCAACTGGCCC | 79734 |
rs855795 | snp | A/C | 0 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052333 | TAGCTCCCTGCACCC[A/C]TCCGCCACCCACATC | 79734 |
rs855796 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052154 | GGCCGCGGCCTGCGT[C/T]GTCCCGTTGCCACGG | 79734 |
rs855797 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050937 | TCAGTTTTTCCACGT[C/T]CTCCCTAAGAAGGAG | 79734 |
rs2142825 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058209 | CACGCCCACCCACAC[A/G]TTCCCTGGCACATGG | 79734 |
rs2235320 | snp | G/T | 0.147656 | 0.228091 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057216 | AGTGAGATGGTGCCT[G/T]GTAAATGCCTGGTGA | 79734 |
rs5756501 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053739 | GCAGGAGAGGGGGGA[A/G]TCTGCTTCCCAGTGG | 79734 |
rs6000544 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057967 | CAGCATTGCAACATG[C/T]AGGGGAGCCCAAAGC | 79734 |
rs6000545 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059200 | TGGGCCCGACAAGCC[A/G]CAAGATTAGGACCTG | 79734 |
rs6000546 | snp | A/G | 0 | 0 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059361 | AGCGAGGACCAGGCA[A/G]AGTTCCTGTGTGTGG | 79734 |
rs6000547 | snp | C/T | 0.117537 | 0.212022 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063788 | CTCCCTTCTCTGACC[C/T]TGCTGGACCCAGCCC | 79734 |
rs7287067 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054440 | TATCTGGGGGCTAGG[A/G]GATCACACAGGGCTA | 79734 |
rs7287458 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054411 | TATCTGGGGGCTAGG[A/G]GATCACACAGGGCTA | 79734 |
rs7287464 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054432 | CACAGGGCTATCTGG[A/G]GGCTAGGAGATCACA | 79734 |
rs7292681 | snp | C/T | 0.104504 | 0.2033 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062157 | ctgctccctgtggct[C/T]ctttcGCCTGGGGCA | 79734 |
rs8138791 | snp | A/G | 0.0655868 | 0.168795 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063499 | CAAAAGCCCAGGGAC[A/G]CTGCCCTGTTGTCAT | 79734 |
rs9610639 | snp | A/T | 0.0376037 | 0.131863 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049953 | TCGttttattttttt[A/T]aaatagagatggggg | 79734 |
rs9610640 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058689 | TTAGCCAGAAGGGCT[A/C]TGTGGGCGTGGTTAT | 79734 |
rs11542756 | snp | C/G | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056394 | CGGATGGAAGAGAAG[C/G]ACTACACGGTCACCC | 79734 |
rs11542757 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063272 | CCATACCCACTCTCC[C/T]CGGGCAGTTCCTGAG | 79734 |
rs11913600 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056095 | CTGGGTCACCGCACT[C/T]AGCACAGCAGAGCTG | 79734 |
rs11913810 | snp | C/G | 0.278664 | 0.248351 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051006 | ACTCGGATCCAGGGC[C/G]TGCTCTACTCTTCCT | 79734 |
rs12159304 | snp | A/C | 0.109814 | 0.206997 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050359 | tcaagcgagccttgg[A/C]ctcccaaagtgctgg | 79734 |
rs12159325 | snp | A/G | 0.134119 | 0.221521 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050261 | ctcaaaaaagaaaaa[A/G]agagagagagagaga | 79734 |
rs12160419 | snp | A/G | 0.0479149 | 0.147179 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051501 | TTTGGGGAAGCCCTC[A/G]TTCTTTTCCCAGAGG | 79734 |
rs12160438 | snp | C/T | 0.0524604 | 0.153226 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051428 | TTATCAGCTGTTGGA[C/T]GACGGAGACGGCACA | 79734 |
rs13054696 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051453 | GGCACAAAGGAAAAA[C/T]AAGAATGCTCGGACC | 79734 |
rs17852877 | snp | C/G | 0 | 0 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051890 | CGGCAGACGCTGTGC[C/G]GCGAGCAGAAGTCCT | 79734 |
rs17852879 | snp | A/C | | | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057463 | CACGCAAATGGTCTC[A/C]ACCATGTCTGATGGC | 79734 |
rs17852880 | snp | C/G | | | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059330 | GGTGAACATCGGCTC[C/G]TCCTACAACTACGGC | 79734 |
rs28412036 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052329 | TTGGGATGTGGGTGG[C/G]GGATGGGTGCAGGGA | 79734 |
rs34289157 | in-del | -/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056004 | TCATGGTGACATTCT[-/G]GGGGATCAGTCCCAA | 79734 |
rs34306072 | in-del | -/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059561 | ACCGCCCATGCACAA[-/C]CCCCATGCTCACAGC | 79734 |
rs34395802 | snp | C/T | 0.000530724 | 0.0162813 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059324 | CTAGCTGGTGAACAT[C/T]GGCTCCTCCTACAAC | 79734 |
rs34493724 | in-del | -/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059030 | TAGGCTGGAGGTGGT[-/G]GGTGGGGACAGCGGT | 79734 |
rs34745899 | in-del | -/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054794 | GGGCACTGGGGATAA[-/T]TTCTCGTAATCAGGC | 79734 |
rs34948303 | in-del | -/A | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050260 | TCTCAAAAAAGAAAA[-/A]GAGAGAGAGAGAGAG | 79734 |
rs35182982 | in-del | -/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059113 | GGTCCTGGGGCACAG[-/T]ACCACAGGCACAGGT | 79734 |
rs35505327 | in-del | -/G | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062298 | CTGGATGGGTTAGTT[-/G]GGGGAGCCCTTGCTG | 79734 |
rs35901190 | snp | A/G | 0.00170555 | 0.0291524 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056357 | CTACAACATCGGCCC[A/G]CTGATCCGCATCATC | 79734 |
rs35975182 | in-del | -/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052056 | ACCCGGCCGGGTTCA[-/T]TTTCCGAGGAACTGG | 79734 |
rs55897262 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059217 | AAGATTAGGACCTGA[A/G]CTGGTATCTTGATTT | 79734 |
rs56126639 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059209 | CAAGCCGCAAGATTA[A/G]GACCTGAGCTGGTAT | 79734 |
rs56340423 | in-del | -/GAGA | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050295 | AGAGAGAGAGAGAGA[-/GAGA]TAGGGGTCTCACTAT | 79734 |
rs56381800 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063432 | GCCACTTTTGGGGAC[A/G]GGGCTAAACTAAAGG | 79734 |
rs56852782 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054275 | AGGCCCCATCGGGAG[G/T]GAAGTAAACACCCCA | 79734 |
rs56979751 | snp | A/C | | | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061423 | GGAGGAGGGGCGCAG[A/C]TGCACCTCCTCTGTG | 79734 |
rs57980010 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055938 | TGCACCTGGCACTTA[A/G]AATGTGCTTAATAAA | 79734 |
rs58201239 | in-del | -/C | 0.0298908 | 0.118541 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061830 | CCATCAGCACCAGAG[-/C]CCAGGCTGGTGGGGA | 79734 |
rs58843694 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059705 | CCGCTTAGTGGCCAC[C/T]GGGCACTGTGGCATG | 79734 |
rs59355258 | in-del | -/AAGA/GA | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050298 | AGAGAGAGAGAGAGA[-/AAGA/GA]TAGGGGTCTCACTAT | 79734 |
rs59772675 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058706 | GTGGGCGTGGTTATT[C/T]TAGGGACCCTGGAAC | 79734 |
rs61214014 | snp | C/G | 0.0349115 | 0.127424 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063419 | CCTCTTTCTCTGGGC[C/G]ACTTTTGGGGACGGG | 79734 |
rs71317024 | snp | A/G | 0.5 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054249 | CATGGGCGTGGCCTA[A/G]GCTCAGGAGCAGGCC | 79734 |
rs71707926 | in-del | -/AA | 0.0524604 | 0.153226 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051400 | GGATTCCTGGAGGGG[-/AA]AGTTTCTTCCCTTAT | 79734 |
rs73415522 | snp | A/C | 0.109814 | 0.206997 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050742 | AGGCCAGGACCAGGA[A/C]TGAAACCAGTAAGGA | 79734 |
rs73884697 | snp | C/G/T | 0.010564 | 0.0719074 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059263 | TCGTATCCTGCCCCA[C/G/T]GGCCCCCAACACCAA | 79734 |
rs73884698 | snp | C/T | 0.0410537 | 0.137264 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062827 | TGTCTCTCCGGCACC[C/T]GCGTCCCCTCTCCCG | 79734 |
rs73886910 | snp | A/G | 0.0298908 | 0.118541 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063051 | GGAAGGACCCAGCCC[A/G]ACCCCTGGGCATAAC | 79734 |
rs73886911 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063310 | GCCAGGGGCCCTCCT[C/G]TGTTTGACTTCCCGG | 79734 |
rs74844925 | snp | C/G | 0.0524604 | 0.153226 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051378 | CACATGCGGGTCAAT[C/G]CTATGGGGATTCCTG | 79734 |
rs75327537 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054777 | CCTGCAGGGCTCCGC[C/T]CAGGGCACTGGGGAT | 79734 |
rs75883417 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052192 | GCTCTCCAGCCGCCC[C/T]GGATCGGGGCCTCTC | 79734 |
rs76442271 | snp | A/G | 0.000339006 | 0.0130149 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056352 | GAGTTCTACAACATC[A/G]GCCCGCTGATCCGCA | 79734 |
rs76498710 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052370 | TGGAGGAGCCCTGGG[G/T]CGCCTTCTGAGCGGG | 79734 |
rs76664375 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054060 | ATCCTGCACCTGTGC[A/G]TGCCTTCCTGCTCTG | 79734 |
rs76833367 | in-del | -/T | 0.448452 | 0.152042 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058506 | GTGTCATGCAAATCA[-/T]TAGAAATCCATATTG | 79734 |
rs77519495 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051520 | TTTTCCCAGAGGCCG[A/G]GAGTTCGACCTTCCC | 79734 |
rs77644444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055110 | TCGCCCGCCCCTTCT[C/T]GAGAGCTTGTTTGGA | 79734 |
rs77673159 | snp | A/G | 0 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059605 | CCCATGCCACCTGCC[A/G]TTACCCAGGCCCAGG | 79734 |
rs78029853 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059834 | AGGATCACATACTCT[C/T]TGTAGTGCCTTGGAG | 79734 |
rs78329095 | snp | C/T | 0.00546817 | 0.0520018 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052612 | CAAGTCGCCTCACCT[C/T]TCAATGTCTCCGATC | 79734 |
rs78379299 | snp | G/T | | | splice-donor-variant | KCTD17 | GRCh38.p7 | 22:37053210 | CATGGCTGAGGAGGG[G/T]GAGTTGGTCCAGGGG | 79734 |
rs78578257 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053355 | CGGGGCTGATTCCCA[A/G]GCATCTGCCTGTGCC | 79734 |
rs79517127 | snp | C/T | 0.0279526 | 0.114869 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051414 | GAAAGTTTCTTCCCT[C/T]ATCAGCTGTTGGACG | 79734 |
rs79570630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055872 | TTTCCCAGTTGTTCA[A/G]TGCAGATGATGAAAG | 79734 |
rs79695422 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057316 | GGGTATGTTGCGGGG[A/G]TGGTGGCAGCAGGTG | 79734 |
rs79883813 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062759 | CAAGGTGGGCCCCAG[A/G]ACCTCTGGGCAGAGT | 79734 |
rs80086725 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054800 | CTGGGGATAATTCTC[A/G]TAATCAGGCAGCTGC | 79734 |
rs80165807 | snp | C/G | 0.0298908 | 0.118541 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049764 | CTTCCTGAGTAGCTG[C/G]AACTACAGGCGTGAG | 79734 |
rs80271594 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059590 | GCCACCGCCATCCAT[C/G]CCATGCCACCTGCCG | 79734 |
rs111412516 | snp | C/T | 0.00527187 | 0.05107 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059466 | GCCTCAGCCTGTGTC[C/T]GGAGAAGTCTCCTGT | 79734 |
rs111459900 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057799 | GAGTCTGTGGCCCCC[A/G]AAGGACAGCTCAGGT | 79734 |
rs111518907 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061467 | CCGGGCACCTCTGAG[A/G]CTGGGCCCTGGCTGC | 79734 |
rs111538548 | snp | A/C | 0.5 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053092 | CCGAGCATCCCTCAC[A/C]TCCATAGGATGAGAC | 79734 |
rs111672049 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054650 | ATCTGTGAAATGGGG[C/G]ACCATAGCACCCACC | 79734 |
rs111832378 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061895 | GTCCCTGCACATCCA[A/G]GAGCTCCTGTGTCAC | 79734 |
rs112009022 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053295 | TTTGGACAACCAGGA[C/T]GGCCATCTGCCTGCT | 79734 |
rs112030530 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057880 | CCTCTTAGAACTCAG[A/G]GTCAGCATCATGCGA | 79734 |
rs112058074 | snp | C/T | 0.0249893 | 0.10895 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052654 | TCGCATGGAAGCCCA[C/T]CCTGCCTCCCTGCCC | 79734 |
rs112358168 | snp | A/G | 0.5 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055563 | GAGCCTAGGGGAGTC[A/G]AAACAGCTGCAAGCT | 79734 |
rs112587587 | snp | C/G | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051752 | AGGATGCAGACGCCG[C/G]GGCCGGCGATGAGGA | 79734 |
rs113014472 | snp | A/C | 0.5 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057003 | ATTAAAGAGGGGAGG[A/C]TCCGTGTCTCCTTGA | 79734 |
rs113075613 | snp | A/G | 0 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060561 | TCATCCCCTCCCTCC[A/G]GCCTCGCTCTATGTA | 79734 |
rs113412072 | in-del | -/G | 0 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061009 | GCTGCAGAACCGGGG[-/G]CCCCGGGGCTGCTGG | 79734 |
rs113509075 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055615 | ACTTCTTCATCTCCC[A/G]GATTAACTTAACTGT | 79734 |
rs113606358 | snp | A/G | 0.5 | 0 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059663 | CAGGGTGCAGCCGGC[A/G]TGGACTCAGAGGCTA | 79734 |
rs113620404 | snp | C/G | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051753 | GGATGCAGACGCCGC[C/G]GCCGGCGATGAGGAT | 79734 |
rs113631038 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060925 | GCACAGGAGAAAGGT[G/T]CAGCCAACCCCCAGG | 79734 |
rs113687833 | snp | A/G | 0.325696 | 0.238265 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051815 | GCGGGCGGCCGCGCC[A/G]CAGGCGGCTGGGGCA | 79734 |
rs113774377 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059103 | GCGGAGGGGCTGGTC[C/T]TGGGGCACAGACCAC | 79734 |
rs114214363 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056244 | GCGAGAGGTGGGTTT[C/T]GGGGTGGAGGGAACA | 79734 |
rs114399920 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054458 | TCACACAGGGCTATC[C/T]GGAGGCTAGGGGATC | 79734 |
rs114579571 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054995 | CTAGAAACCCGAGAT[C/T]GGGGCACTGTGGCAG | 79734 |
rs115223028 | snp | C/T | 0.0244538 | 0.107838 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063714 | TGGGCCACCGCCATC[C/T]CTCCCTATTGCTGCC | 79734 |
rs115352795 | snp | A/G | 0.00217126 | 0.0328772 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052641 | TCTCTCTGTAGAGTC[A/G]CATGGAAGCCCACCC | 79734 |
rs115646797 | snp | A/C | 0.00755907 | 0.0610114 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063491 | CTTTGTCCCAAAAGC[A/C]CAGGGACGCTGCCCT | 79734 |
rs115868224 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052836 | AGACATCCTCTCACC[G/T]GATGCTCACAGCAAA | 79734 |
rs116036463 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050357 | GCTCAAGCGAGCCTT[A/G]GCCTCCCAAAGTGCT | 79734 |
rs116163897 | snp | A/G | 0.0535932 | 0.154675 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051293 | ACTCAGGTGAGGGAA[A/G]GAACCCACTCCCACC | 79734 |
rs116790622 | snp | C/G/T | 0.00835141 | 0.0640778 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054151 | TCTAATAGGTCAGGG[C/G/T]CACAACACCAGAGTC | 79734 |
rs116797316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058368 | GTTACATCTCCTGTG[C/T]GGGACCCAGTTCCCT | 79734 |
rs116956945 | snp | C/T | 0.0771109 | 0.180581 | synonymous-codon, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062546 | CAAGCCAGAGGCACC[C/T]GGATGTGAGGCCCCA | 79734 |
rs117217366 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058196 | GCTAGCCTTTCTCCA[C/T]GCCCACCCACACGTT | 79734 |
rs117279873 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056218 | GCTCACCCTCAGGGC[A/G]GGTGATCAGAGCGAG | 79734 |
rs117374713 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055046 | CCGGATTGCAGACTG[C/T]TGACTTCTCGTTGTG | 79734 |
rs117406281 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058444 | GAGATTAGAAGGGCC[A/C]TCAGTAAAGCTTACA | 79734 |
rs117835696 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054355 | TGCTATTCCCACACC[A/G]TCAGACAGCGCTGTC | 79734 |
rs117888732 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055583 | AGCTGCAAGCTCATC[A/G]CTTCACTGGTGGGCT | 79734 |
rs118164763 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058066 | GGAGATCCTTATCCC[A/G]AGGGACTTTATCCCT | 79734 |
rs138419814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055668 | CTCTCCTCATATCCC[C/T]GGACTTGTGATGAGC | 79734 |
rs138776174 | snp | C/T | 0.000812348 | 0.0201374 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052651 | GAGTCGCATGGAAGC[C/T]CACCCTGCCTCCCTG | 79734 |
rs138793540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058718 | ATTCTAGGGACCCTG[C/G]AACAAGGGCAGGGCC | 79734 |
rs138994810 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056099 | GTCACCGCACTCAGC[A/G]CAGCAGAGCTGTGTG | 79734 |
rs139968480 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053415 | TCAAGCTTTCCCTGG[A/G]TACTGTCAGGGAGGT | 79734 |
rs140208779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057679 | TGGTGGCAGGTTGAC[C/T]GAGAGAGAGGATAGG | 79734 |
rs140419478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055492 | ATAATGAGCTCTGTC[C/T]CCAGGGAGCCCAGAG | 79734 |
rs140838957 | snp | C/T | 0.000238209 | 0.0109109 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057482 | ATGTCTGATGGCTGG[C/T]GCTTCGAGCAGGTGC | 79734 |
rs140892281 | snp | C/T | 0.0023933 | 0.0345097 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063650 | CCTGGGCTGCCTCTG[C/T]CACATCCTAAACCTC | 79734 |
rs141007221 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051084 | CAGGAAAGAGACCTT[G/T]GTGGGTACTCACTCA | 79734 |
rs141374146 | in-del | -/CCT | 0.0232847 | 0.105357 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062237 | CTTGGCAGAATCTGG[-/CCT]CCTCTGTAGGTGGCC | 79734 |
rs141435455 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059674 | CGGCGTGGACTCAGA[A/G]GCTACATGAAGGGGG | 79734 |
rs141452749 | snp | C/G | 0.0150606 | 0.0854603 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050094 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCAGGC | 79734 |
rs141598415 | snp | C/T | 3.23013e-05 | 0.00401866 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053166 | ATCCTGAACTTCCTC[C/T]GGCATGGCAAGCTGG | 79734 |
rs141755881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055604 | CTGGTGGGCTGACTT[C/T]TTCATCTCCCAGATT | 79734 |
rs141827097 | snp | G/T | 0.00898165 | 0.066409 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052657 | CATGGAAGCCCACCC[G/T]GCCTCCCTGCCCGCC | 79734 |
rs142445922 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058847 | AGTGGACCACCTGTC[A/G]TCCCACCTCTGCTTC | 79734 |
rs142525657 | snp | C/T | 0.0240643 | 0.107019 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063471 | TCTGGTCCAAAGGAA[C/T]GCGGCTTTGTCCCAA | 79734 |
rs142739650 | snp | C/T | 0.000429069 | 0.0146407 | synonymous-codon, utr-variant-3-prime, stop-gained, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062531 | TTTTTCTAGCTGTTA[C/T]AAGCCAGAGGCACCC | 79734 |
rs142940186 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057059 | AGAATGTTCCCTAAG[C/T]CCCACCCATGTTCTT | 79734 |
rs143143656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058626 | GATTCTCTTCAGGGT[C/T]CCTGAGAGCTGAATG | 79734 |
rs143231972 | snp | C/T | 0.00117137 | 0.0241725 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057338 | CAGCAGGTGCTCATG[C/T]CCCTCCTGGGGTGCC | 79734 |
rs143272755 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061954 | GGATGGGGAGGACAG[A/G]CCACTTTTGGATACC | 79734 |
rs143403650 | snp | A/G/T | 0.00022664 | 0.010643 | missense, stop-gained, utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062547 | AAGCCAGAGGCACCC[A/G/T]GATGTGAGGCCCCAG | 79734 |
rs143582237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055524 | CCAGTCAAGGAAAGG[A/G]CCCAAAGGTCCCCTG | 79734 |
rs144598860 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052220 | CTCCTTCTCCTTTGG[A/G]GCTGTGGACAGGGAG | 79734 |
rs144618366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055327 | AGTGACAGATGTCCC[C/T]GCCAGATCGCCCTCA | 79734 |
rs144682183 | snp | C/G | 8.3212e-05 | 0.00644973 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059395 | CCAAGGAGCTCCACA[C/G]CACCCCAAACGGGCT | 79734 |
rs144758579 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053360 | CTGATTCCCAAGCAT[C/T]TGCCTGTGCCGAGCC | 79734 |
rs144854301 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051125 | GAGTAGGGCGGTCAC[C/T]TCGCTTCTGTGGCTT | 79734 |
rs144863839 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056542 | GGGAGGCCGAGCTGG[A/C]CTGTAAGGAGAGGCA | 79734 |
rs144894099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054288 | AGGGAAGTAAACACC[C/T]CAGCTGCGTCGCAGC | 79734 |
rs144967947 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055063 | GACTTCTCGTTGTGT[C/T]CTCACATGGCAGAAA | 79734 |
rs145128609 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058242 | ACTGCAAGGCAGAAG[A/G/T]TCGGAGCCCCCAGGA | 79734 |
rs145348916 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050942 | TCTTAGGGAGGACGT[C/G]GAAAAACTGAGAAAG | 79734 |
rs145799693 | snp | C/T | 0.0271762 | 0.113356 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051279 | GTCGTTCTCCAAGAA[C/T]TCAGGTGAGGGAAAG | 79734 |
rs145848141 | in-del | -/GG | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063288 | GAGAGTGGGTATGGC[-/GG]GGCTGAGCCAGGGGC | 79734 |
rs146127576 | snp | A/G | 0.00356445 | 0.0420657 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061545 | TCCTTGCAGGTTCCC[A/G]TCCGCACCCTCTCAG | 79734 |
rs146227286 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062144 | TTGGGACAGACAGCT[A/G]CTCCCTGTGGCTTCT | 79734 |
rs146468443 | snp | A/G | 5.38904e-05 | 0.0051906 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059472 | GCCTGTGTCCGGAGA[A/G]GTCTCCTGTCTCCCT | 79734 |
rs146513411 | snp | A/G | 3.56075e-05 | 0.0042193 | missense, utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062532 | TTTTCTAGCTGTTAC[A/G]AGCCAGAGGCACCCG | 79734 |
rs146656531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055478 | CACACATTCTGCTCA[G/T]AATGAGCTCTGTCCC | 79734 |
rs146668214 | snp | C/T | 1.6612e-05 | 0.00288196 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057448 | CCAGGAGGAGGAGCT[C/T]ACGCAAATGGTCTCC | 79734 |
rs146711968 | snp | C/G | 0.00304939 | 0.0389281 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062565 | TGTGAGGCCCCAGAT[C/G]ACCTCCAGGGACTTG | 79734 |
rs147239946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053913 | GTTAACTCTTCTTTG[G/T]GACACAGGGTGTGGC | 79734 |
rs147250087 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055924 | ATTCAAAAATGTAAT[A/G]CACCTGGCACTTAGA | 79734 |
rs147755951 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051002 | CCTGACTCGGATCCA[A/G]GGCGTGCTCTACTCT | 79734 |
rs147970401 | snp | C/G | 6.46977e-05 | 0.00568724 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053165 | CATCCTGAACTTCCT[C/G]CGGCATGGCAAGCTG | 79734 |
rs148425103 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063010 | GCAGTATATAGGGGC[C/T]GCCCACCTTCAGCTG | 79734 |
rs148582611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056796 | TGCAGGATTAGCAAA[C/T]TGTGCCTTTTGTGGC | 79734 |
rs148599535 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057611 | ACCACAGTCTCCCCC[-/A]ACCCCAGGGTTCTTC | 79734 |
rs149106452 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058300 | TAGTGCAGAGCCAGA[A/G]GCCTGGCTTCACCTC | 79734 |
rs149432408 | snp | A/G | 0.00168074 | 0.0289404 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056417 | GGTCACCCAGGTCGG[A/G]AGCAGGGGCAGCACA | 79734 |
rs149632662 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061018 | CCGGGGGCCCCGGGG[A/C]TGCTGGGGGGGCACC | 79734 |
rs149735301 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063881 | CGAGGAAATCCTGCC[A/G]GGCAGTGAGCCCCTA | 79734 |
rs149785422 | snp | C/T | 1.65996e-05 | 0.00288089 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059313 | GCTCCGCCCCTCTAG[C/T]TGGTGAACATCGGCT | 79734 |
rs149875918 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057974 | GCAACATGCAGGGGA[A/G]CCCAAAGCAGTGCCT | 79734 |
rs150034371 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054858 | GTCCTGTGTGGGCAC[C/T]GGGGACAGAGGGCAG | 79734 |
rs150355415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052792 | CAGAGGGACATTCTT[C/T]GAGCCCTGTGCTGGG | 79734 |
rs150660811 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057136 | GGGTGACCTTGGGCA[A/G]GTAACTGGACCTCTC | 79734 |
rs150819749 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060007 | AGGGGCAGCCTGGTG[G/T]CTGCCAGTCCTGTGT | 79734 |
rs150904187 | snp | C/T | 3.45471e-05 | 0.004156 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056336 | GGTCCTGGAGGAAGC[C/T]GAGTTCTACAACATC | 79734 |
rs150924179 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063552 | GGGCTTGGGGAACTG[A/G]CTATATCCTTTGCCC | 79734 |
rs151210069 | in-del | -/AT | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054927 | CAATCATGAAGTAAC[-/AT]AGATTGGGTGGCTTA | 79734 |
rs151303523 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054342 | ATTCTCAAAGCCCTG[C/G]TATTCCCACACCGTC | 79734 |
rs180708556 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063178 | GATCCCACCCCCAGC[C/T]ATTTGCATTGCTGGC | 79734 |
rs181267058 | snp | A/C | 0.0111196 | 0.0737302 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063872 | CCCGCTGCTCGAGGA[A/C]ATCCTGCCGGGCAGT | 79734 |
rs181524900 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056727 | CACACCCATCCCTTC[C/T]TCATAGGCAGAAGGG | 79734 |
rs181921639 | snp | A/G | 1.88457e-05 | 0.00306961 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057367 | CCTGGTGCTCCCACA[A/G]GTGCCCTCTATGTGA | 79734 |
rs181998171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060763 | GGATAGCCAGCAGGC[C/T]CTGGCCCCTCTGTTA | 79734 |
rs182130956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054933 | TGAAGTAACATAGAT[C/T]GGGTGGCTTATGAAA | 79734 |
rs182503453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054807 | TAATTCTCGTAATCA[A/G]GCAGCTGCACTCCCT | 79734 |
rs182758043 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051312 | CCCACTCCCACCCAC[C/G]CCGCCCCCACCCCTA | 79734 |
rs182911376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055246 | GACACACCTGGAGCA[A/G]TGAGGGAGGAAGGGG | 79734 |
rs183182443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058976 | CCGCCCTTTAGAGGC[C/T]TCCGCCTGCATTTAG | 79734 |
rs183235525 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058557 | GGACTTGGGATCCCC[A/G/T]ATGCCATTCCCTGCT | 79734 |
rs183345487 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058092 | TCCCTAGTCATGCAG[A/C]TGACCTCCCACCTTT | 79734 |
rs183791733 | snp | C/T | 0.000896737 | 0.0211557 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056435 | CAGGGGCAGCACACA[C/T]GGCCAGGGCAGGGGC | 79734 |
rs183827506 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049791 | TGAGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 79734 |
rs184018493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053296 | TTGGACAACCAGGAC[A/G]GCCATCTGCCTGCTT | 79734 |
rs184104897 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055952 | AGAATGTGCTTAATA[A/C]ATAGGAGCACATAAT | 79734 |
rs184367191 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051517 | TTCTTTTCCCAGAGG[A/C]CGGGAGTTCGACCTT | 79734 |
rs184661225 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056668 | CAGGCTCGCCCTCTC[C/T]GGACCTTGATTTTCT | 79734 |
rs184785910 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061418 | CCTGGGGAGGAGGGG[C/T]GCAGCTGCACCTCCT | 79734 |
rs185364748 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059764 | TCTCTGTGTGACTTA[A/G]GACAGGGCTTGTCCT | 79734 |
rs185458887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052638 | CGATCTCTCTGTAGA[A/G]TCGCATGGAAGCCCA | 79734 |
rs185726024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054989 | TAGAGGCTAGAAACC[C/G]GAGATCGGGGCACTG | 79734 |
rs186206600 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058415 | TAACAGTACCTCCTC[A/T]GTAGGACTCTTGTGA | 79734 |
rs186557908 | snp | C/G | 0.00953873 | 0.0683987 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063691 | CCCTCCACTTCTACT[C/G]TGACACCTGGGCCAC | 79734 |
rs186753872 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059072 | CCTCCACCAGGGATC[A/G]GGCCAGCCAAGCCAG | 79734 |
rs187048348 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051419 | TTTCTTCCCTTATCA[G/T]CTGTTGGACGACGGA | 79734 |
rs187085280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054815 | GTAATCAGGCAGCTG[C/T]ACTCCCTGACCTCCT | 79734 |
rs187134464 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054444 | TGGGGGCTAGGAGAT[C/T]ACACAGGGCTATCCG | 79734 |
rs187354032 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058589 | CACCCCTTCCTAGCT[A/G]TGAGGCCTTCAGCAG | 79734 |
rs187434191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057007 | AAGAGGGGAGGCTCC[A/G]TGTCTCCTTGAGGGC | 79734 |
rs187827072 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059699 | AGGGGGCCGCTTAGT[G/T]GCCACTGGGCACTGT | 79734 |
rs188005739 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050481 | ACTGTTGTAAATCCC[A/C]TTTGGCAAGAGAGAA | 79734 |
rs188116230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056482 | GCTGAGAGACGGGGC[A/G]GGAAGCAGAGGAGGT | 79734 |
rs188337530 | snp | A/G | 0.000978599 | 0.0220985 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062628 | CATGGGGTGGGCCCC[A/G]GGCCTGAGAAGGAAG | 79734 |
rs188356924 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061140 | CTAACCTTTTCTCCC[C/T]CCCACCACTGCCTCC | 79734 |
rs188358242 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054417 | GGGGCTAGGGGATCA[A/C]ACAGGGCTATCTGGG | 79734 |
rs188376161 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052157 | TGGCAACGGGACGAC[A/G]CAGGCCGCGGCCATT | 79734 |
rs188610113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056061 | AAAGCTGCCCCAGAC[A/G]GTGGCCTGGCAGGTA | 79734 |
rs188762850 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055582 | CAGCTGCAAGCTCAT[C/T]GCTTCACTGGTGGGC | 79734 |
rs189047094 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060614 | AGCATGCCCACAGCA[C/T]CCCATCCTCAGCTGC | 79734 |
rs189290757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057096 | ATTACCCGTGTTCCG[G/T]TTCTGTCTCCTTCAC | 79734 |
rs189534588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052740 | AAGCCTAGGGACCTG[A/G]GGGCGACAGTGGGGC | 79734 |
rs189747877 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057931 | GTTTTCAGGGTCTCC[A/G]CAGGGGACATGCCCA | 79734 |
rs189764005 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051160 | TGTAAAATGGGTATA[G/T]CCCAAAATACCAGAC | 79734 |
rs189917009 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054826 | GCTGCACTCCCTGAC[C/T]TCCTGCTCTGTGTTT | 79734 |
rs189927842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054696 | GAGGATAAAAGGAGT[C/T]AATAGTGCAGCATGG | 79734 |
rs190329035 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056675 | GCCCTCTCCGGACCT[A/T]GATTTTCTCTTATGG | 79734 |
rs190442562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055101 | AGCTAGCCCTCGCCC[A/G]CCCCTTCTCGAGAGC | 79734 |
rs191139650 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053036 | CTTCCCTCCCTGTGC[A/C/G]TGTGCGGGGTTGGCT | 79734 |
rs191289945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056090 | TACCCCTGGGTCACC[A/G]CACTCAGCACAGCAG | 79734 |
rs191365557 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063742 | GCCACCCCTCTGCCC[A/C]AAATCCTAGGAAATA | 79734 |
rs191826136 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056659 | GTGTTGGGCCAGGCT[C/T]GCCCTCTCCGGACCT | 79734 |
rs191905701 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058466 | AAGCTTACAGCCCTC[C/T]GTAGGACTCCCTATG | 79734 |
rs192201865 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051489 | GATGACTGCAGATTT[C/G]GGGAAGCCCTCATTC | 79734 |
rs192215589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059239 | TCTTGATTTGAGTGC[C/T]GAGGTCTGTCGTATC | 79734 |
rs192660353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058846 | GAGTGGACCACCTGT[C/T]GTCCCACCTCTGCTT | 79734 |
rs192843950 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055639 | TAACTGTAAGATGGG[G/T]ACAGTAATGCCTGCT | 79734 |
rs193159692 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059700 | GGGGGCCGCTTAGTG[C/G]CCACTGGGCACTGTG | 79734 |
rs193284428 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052274 | CCAAAGGGGACTCCT[A/G]CTCTGGGGAAGGAGT | 79734 |
rs199630377 | snp | C/T | 0.000669496 | 0.0182839 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061491 | TGGCTGCAGGCCCTG[C/T]CCCCCCTCCTCTCCT | 79734 |
rs199711104 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050387 | TGGGATTACAGGTGT[A/G]AGCCACCGCACCCAG | 79734 |
rs199799512 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052531 | GTAACACGAAGGGCT[G/T]GTCTGAAGATGACCT | 79734 |
rs199921196 | snp | C/T | 0.00037808 | 0.013744 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061607 | CCTCGGCCCCTCGCC[C/T]GCCCCCAGAGCTGCC | 79734 |
rs199931970 | snp | C/T | 0.000358125 | 0.0133766 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062604 | ATCTGAAATCCTTTA[C/T]TTTTGTACCATGGGG | 79734 |
rs200219289 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051980 | TGGGCGGCGAGCGGG[C/T]GGTGGGTCCTCCGCT | 79734 |
rs200563649 | snp | A/G | 0.000663306 | 0.0181993 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059325 | TAGCTGGTGAACATC[A/G]GCTCCTCCTACAACT | 79734 |
rs200857047 | snp | A/C/G | 0.00104912 | 0.0228812 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061496 | GCAGGCCCTGCCCCC[A/C/G]CTCCTCTCCTCCCGG | 79734 |
rs200992863 | snp | C/T | 0.000149637 | 0.00864848 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059279 | GGCCCCCAACACCAA[C/T]CTGCATTTTTCTCCC | 79734 |
rs201383375 | snp | A/G | 0.000106212 | 0.0072866 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057498 | GCTTCGAGCAGGTGC[A/G]CTGGGGACAGGGGCG | 79734 |
rs201608256 | snp | A/C/G | 0.000282043 | 0.0118725 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061495 | TGCAGGCCCTGCCCC[A/C/G]CCTCCTCTCCTCCCG | 79734 |
rs201717740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054012 | TCTATTCAATGGGGG[C/T]GGTGATCTGCCTTCT | 79734 |
rs207477988 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059261 | TGTCGTATCCTGCCC[C/T]ACGGCCCCCAACACC | 79734 |
rs367788732 | snp | A/G | 4.37436e-05 | 0.00467652 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053221 | AGGGTGAGTTGGTCC[A/G]GGGGGCTGGCCTGGA | 79734 |
rs367800128 | in-del | -/TC | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062409 | CTGCCTCTCTCTCTC[-/TC]CCTCTCCCCCACCCG | 79734 |
rs368081178 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061497 | CAGGCCCTGCCCCCC[C/G/T]TCCTCTCCTCCCGGC | 79734 |
rs368084723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059940 | GATGAGGAAGCCACC[A/G]CTGTAAATCCTGCCC | 79734 |
rs368089936 | snp | A/T | 1.67939e-05 | 0.0028977 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057472 | GGTCTCCACCATGTC[A/T]GATGGCTGGCGCTTC | 79734 |
rs368099793 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051213 | AATTCATAACACATA[C/T]ACACAAAGTGTCTGG | 79734 |
rs368402919 | snp | C/T | 0.000135694 | 0.00823582 | intron-variant, synonymous-codon | KCTD17 | GRCh38.p7 | 22:37061666 | GAGGGAGGGGTGGAG[C/T]GAGGAGGGTGCTCAT | 79734 |
rs368639961 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055445 | CACAGTTTTCAGCAG[A/G]TGGATTTTTGGGGAA | 79734 |
rs368650232 | snp | C/G/T | 0.000379965 | 0.0137782 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059450 | CAAGGTGAGCCCACC[C/G/T]GCCTCAGCCTGTGTC | 79734 |
rs369009490 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062512 | TCCTGCCCTTCCCCT[C/T]TTTTTTTTCTAGCTG | 79734 |
rs369047167 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052859 | ACAGCAAACCCTGAT[G/T]AGGGGGAGAGGAGTG | 79734 |
rs369063295 | snp | A/G | 0.00506682 | 0.0500773 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052512 | TCAGCCTCCTTCCTC[A/G]TCTGTAACACGAAGG | 79734 |
rs369091372 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056440 | GCAGCACACACGGCC[A/C]GGGCAGGGGCCAGTG | 79734 |
rs369203695 | snp | C/T | 1.66275e-05 | 0.00288331 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059280 | GCCCCCAACACCAAC[C/T]TGCATTTTTCTCCCC | 79734 |
rs369269761 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061856 | GGGGAGGGAGGGACC[A/G]CTGAAGCCAGAGGCC | 79734 |
rs369333840 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050450 | TTAATCTTCACAGCA[A/G]TGCTCTGGGGTCACA | 79734 |
rs369557121 | snp | G/T | 7.2223e-05 | 0.00600885 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057504 | AGCAGGTGCGCTGGG[G/T]ACAGGGGCGTGCCAC | 79734 |
rs369712120 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050230 | CTCCAGTCTGGGTGA[A/G]AGAGTGAGACTGTAT | 79734 |
rs369869536 | snp | A/G | 6.65646e-05 | 0.0057687 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059264 | CGTATCCTGCCCCAC[A/G]GCCCCCAACACCAAC | 79734 |
rs370083021 | snp | A/C/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050784 | GGAGACAGCTTCCTC[A/C/G]TCAGCCCTTGTCCCT | 79734 |
rs370142358 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050068 | AGCCTGGCCAACGTG[A/G]TGAAACCCTATCTCT | 79734 |
rs370156130 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059192 | CCCAGGAGTGGGCCC[A/G]ACAAGCCGCAAGATT | 79734 |
rs370177467 | snp | A/G | 0.000140598 | 0.00838326 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060916 | GAGGCAGATGCACAG[A/G]AGAAAGGTGCAGCCA | 79734 |
rs370300983 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055033 | TGAGGACTTTCTTCC[A/G]GATTGCAGACTGCTG | 79734 |
rs370524800 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058106 | GCTGACCTCCCACCT[C/T]TCAGGTTTCCAGAGG | 79734 |
rs370564833 | snp | C/T | | | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063603 | CCTGCCCTACCTGGC[C/T]GGGAGCCAGAAAACA | 79734 |
rs370740376 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054405 | CAGGGTTATCTGGGG[C/G]CTAGGGGATCACACA | 79734 |
rs370855894 | snp | C/T | 0.000101216 | 0.00711322 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056401 | AAGAGAAGGACTACA[C/T]GGTCACCCAGGTCGG | 79734 |
rs370948832 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050994 | TCAGTTCTCCTGACT[C/T]GGATCCAGGGCGTGC | 79734 |
rs370950840 | snp | A/C/T | 0.000318108 | 0.0126077 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062631 | GGGGTGGGCCCCGGG[A/C/T]CTGAGAAGGAAGAAG | 79734 |
rs370992567 | snp | C/G/T | 0.000231636 | 0.0107598 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053108 | TCCATAGGATGAGAC[C/G/T]GGGGCCTACCTCATT | 79734 |
rs371024912 | snp | A/G | 0.000107189 | 0.00732005 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061524 | CGGCCTCCTCCTCAC[A/G]TTTCCTCCTTGCAGG | 79734 |
rs371113714 | snp | A/G | 8.85105e-05 | 0.00665187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059463 | CCCGCCTCAGCCTGT[A/G]TCCGGAGAAGTCTCC | 79734 |
rs371310195 | snp | G/T | 0.000157988 | 0.00888645 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053256 | ATGCAGCCTGCCAGG[G/T]CCCTCTGTGGAGGCC | 79734 |
rs371364276 | in-del | -/GAGAGAGAGAGA | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050287 | AGAGAGAGAGAGAGA[-/GAGAGAGAGAGA]TAGGGGTCTCACTAT | 79734 |
rs371676360 | snp | C/G | 2.14484e-05 | 0.00327471 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061610 | CGGCCCCTCGCCCGC[C/G]CCCAGAGCTGCCATC | 79734 |
rs371727118 | snp | C/T | 2.81219e-05 | 0.00374969 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062476 | CCCTCCTTACCGGCC[C/T]CACCTCCGCCCCTCC | 79734 |
rs371921045 | snp | A/G | 0.000103639 | 0.00719785 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056436 | AGGGGCAGCACACAC[A/G]GCCAGGGCAGGGGCC | 79734 |
rs371968782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055576 | TCGAAACAGCTGCAA[A/G]CTCATCGCTTCACTG | 79734 |
rs372021490 | snp | C/T | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051816 | CGGGCGGCCGCGCCG[C/T]AGGCGGCTGGGGCAA | 79734 |
rs372123634 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058479 | TCCGTAGGACTCCCT[A/G]TGTTGGCATTAGTGT | 79734 |
rs372384887 | snp | A/G | 9.10821e-05 | 0.0067478 | missense, synonymous-codon, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061565 | CACCCTCTCAGACCT[A/G]AGGCTGAGCTTGCAG | 79734 |
rs372514917 | snp | A/G | 0.00121943 | 0.0246623 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052646 | CTGTAGAGTCGCATG[A/G]AAGCCCACCCTGCCT | 79734 |
rs372569746 | snp | C/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062633 | GGTGGGCCCCGGGCC[C/T]GAGAAGGAAGAAGCA | 79734 |
rs372596626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062124 | GGCCACAATTGCCTC[C/T]AAAATTGGGACAGAC | 79734 |
rs372692411 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055107 | CCCTCGCCCGCCCCT[C/T]CTCGAGAGCTTGTTT | 79734 |
rs372826685 | snp | C/T | 8.48673e-05 | 0.00651356 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056351 | CGAGTTCTACAACAT[C/T]GGCCCGCTGATCCGC | 79734 |
rs372989339 | snp | A/G | 7.44214e-05 | 0.0060996 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057513 | GCTGGGGACAGGGGC[A/G]TGCCACCAGGACAAC | 79734 |
rs373025155 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063292 | GTGGGTATGGCGGCT[-/G]GAGCCAGGGGCCCTC | 79734 |
rs373149200 | snp | C/G | 1.66391e-05 | 0.00288431 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059267 | ATCCTGCCCCACGGC[C/G]CCCAACACCAACCTG | 79734 |
rs373194937 | snp | A/C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053890 | GCAAGGACTACAGTC[A/C/G]GTGCCAAGTTAACTC | 79734 |
rs373561260 | snp | A/C | 0.0115144 | 0.0749975 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063630 | AACAGAACTCTAGGG[A/C]GAGCCCTGGGCTGCC | 79734 |
rs373712157 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059662 | CCAGGGTGCAGCCGG[C/T]GTGGACTCAGAGGCT | 79734 |
rs373819500 | snp | A/G | 1.66131e-05 | 0.00288206 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059383 | TGTGTGTGGTGTCCA[A/G]GGAGCTCCACAGCAC | 79734 |
rs373925933 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063247 | GGGGCTGGGCAGGGG[C/T]GGTGGAGGACTCAGG | 79734 |
rs374182123 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062716 | CCTCCAGGGGCGGGG[C/T]GGGGCCCCCCTGGGA | 79734 |
rs374305148 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062841 | CTGCGTCCCCTCTCC[C/T]GGGCTCCCCTGCTGC | 79734 |
rs374499572 | snp | C/G | 0.00114966 | 0.023948 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053217 | GAGGAGGGTGAGTTG[C/G]TCCAGGGGGCTGGCC | 79734 |
rs374610078 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050880 | TCCCCTCCGAGTTAA[C/T]TGGGGAATAACTCAG | 79734 |
rs374677967 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056881 | CCTTGGAGCCTGGGC[C/T]TCCCTGGCCAGTCTG | 79734 |
rs374689494 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055043 | CTTCCGGATTGCAGA[C/T]TGCTGACTTCTCGTT | 79734 |
rs374873176 | snp | C/T | 0.000140872 | 0.00839144 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057497 | CGCTTCGAGCAGGTG[C/T]GCTGGGGACAGGGGC | 79734 |
rs374876906 | snp | C/T | 1.67301e-05 | 0.00289219 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057404 | TGCCCACAGGTCCCA[C/T]CCAAGCACGTGTACC | 79734 |
rs375212098 | in-del | -/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056845 | GGCTCGGCACAGGCT[-/G]GTTGGGGCTGGCGTT | 79734 |
rs375397105 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054505 | GGGCTAGGGGATCAC[A/G]CAGGGCTATCCGGGG | 79734 |
rs375434431 | snp | C/T | 4.08147e-05 | 0.00451726 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061529 | TCCTCCTCACGTTTC[C/T]TCCTTGCAGGTTCCC | 79734 |
rs375449790 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37061059 | CAGCCACTTGCCTGG[C/T]GCCTCACCCGCATAA | 79734 |
rs375647465 | in-del | -/T | | | intron-variant, frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061310 | GCCCTGGTCCCAGCC[-/T]CCCGTGCCCTCCACC | 79734 |
rs375665017 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059201 | GGGCCCGACAAGCCG[C/T]AAGATTAGGACCTGA | 79734 |
rs375791343 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055267 | GAGGAAGGGGACACA[C/T]ATCTAGCCAGCCAGA | 79734 |
rs376044186 | in-del | -/AGAT | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050296 | GAGAGAGAGAGAGAG[-/AGAT]AGGGGTCTCACTATG | 79734 |
rs376174681 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053715 | GCACAGTGCTGGCTG[G/T]GGGTGGAGGCAGGAG | 79734 |
rs376248990 | snp | C/T | 1.66103e-05 | 0.00288182 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059301 | TTTTCTCCCCATGCT[C/T]CGCCCCTCTAGCTGG | 79734 |
rs376293639 | snp | A/G | 0.000153988 | 0.00877328 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062640 | CCCGGGCCTGAGAAG[A/G]AAGAAGCACCCTCTC | 79734 |
rs376418254 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050961 | AAACTGAGAAAGGCC[A/G]AAAGCCAGAATGGAA | 79734 |
rs376443463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053035 | CCTTCCCTCCCTGTG[C/T]GTGTGCGGGGTTGGC | 79734 |
rs376451630 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059691 | CTACATGAAGGGGGC[C/T]GCTTAGTGGCCACTG | 79734 |
rs376480859 | snp | A/G | 0.00835141 | 0.0640778 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063434 | CACTTTTGGGGACGG[A/G]GCTAAACTAAAGGTG | 79734 |
rs376503446 | in-del | -/CTC | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062241 | GCAGAATCTGGCCTC[-/CTC]TGTAGGTGGCCGCCA | 79734 |
rs376509166 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050395 | CAGGTGTGAGCCACC[A/G]CACCCAGCCTACGCT | 79734 |
rs376815052 | snp | C/T | 8.30558e-05 | 0.00644368 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059302 | TTTCTCCCCATGCTC[C/T]GCCCCTCTAGCTGGT | 79734 |
rs377210886 | snp | C/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049849 | TGGCCAGGCTGGTCT[C/G]GAACTCCTGACCTTG | 79734 |
rs377308609 | snp | C/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051632 | GGGGGCGGGAGCAGC[C/G]CGGGGCGGGACCCTA | 79734 |
rs377530202 | snp | C/T | 0.000157418 | 0.00887042 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053078 | TCACTCTTCTCTCAC[C/T]GAGCATCCCTCACCT | 79734 |
rs377601872 | snp | A/G | 3.51185e-05 | 0.00419023 | missense, utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062541 | TGTTACAAGCCAGAG[A/G]CACCCGGATGTGAGG | 79734 |
rs377623859 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062792 | ACTGCTCATGGCAGA[C/T]GTGTGGCAATGTCTG | 79734 |
rs386821160 | in-del | A/GAGAGAGAGAGAG | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050261 | CTCAAAAAAGAAAAA[A/GAGAGAGAGAGAG]AGAGAGAGAGAGAGA | 79734 |
rs397812064 | in-del | -/C | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061832 | ATCAGCACCAGAGCC[-/C]AGGCTGGTGGGGAGG | 79734 |
rs527744133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056701 | TATGGGATAGAGAGG[A/G]GTGGGAATGGCACAC | 79734 |
rs527746530 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050792 | CTTCCTCGTCAGCCC[G/T]TGTCCCTCCCTGGTC | 79734 |
rs527878635 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056245 | CGAGAGGTGGGTTTC[A/G]GGGTGGAGGGAACAA | 79734 |
rs528465889 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060326 | CACTGCCAGGGCTGA[C/T]GCTGCCCTGCAAGGG | 79734 |
rs528902797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054139 | GCCCAGCAACTCTCT[A/G]ATAGGTCAGGGCCAC | 79734 |
rs529549036 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057313 | TTTGGGTATGTTGCG[C/G]GGGTGGTGGCAGCAG | 79734 |
rs529688110 | snp | C/T | 0.00318978 | 0.0398085 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063431 | GGCCACTTTTGGGGA[C/T]GGGGCTAAACTAAAG | 79734 |
rs529895350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057311 | TCTTTGGGTATGTTG[C/T]GGGGGTGGTGGCAGC | 79734 |
rs530018535 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050671 | GGCTGCCCAGTGTTC[A/G]GGCCAGCTGCGTGTG | 79734 |
rs530167799 | snp | A/G | 2.42886e-05 | 0.00348479 | splice-donor-variant, intron-variant, stop-gained | KCTD17 | GRCh38.p7 | 22:37061630 | GAGCTGCCATCCCTG[A/G]TTTGTAGCTTGGCGG | 79734 |
rs530227681 | snp | A/G | 0.000798403 | 0.0199641 | synonymous-codon, intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061162 | ACTGCCTCCTCCTCC[A/G]CTTCCCGCTGGAGGT | 79734 |
rs530742368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054671 | AGCACCCACCTCACC[A/G]AGCTGTCATGAGGAT | 79734 |
rs530750560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060181 | GCAGGCGTGAACCAG[C/G]CTGGGAAGAAGGCAG | 79734 |
rs530922287 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057054 | GACCCAGAATGTTCC[C/G]TAAGCCCCACCCATG | 79734 |
rs531186109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053395 | GCTCTGCCAAGCGGA[C/T]GGGCTCAAGCTTTCC | 79734 |
rs531259647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058073 | CTTATCCCGAGGGAC[C/T]TTATCCCTAGTCATG | 79734 |
rs531428348 | in-del | -/C | 0.00318978 | 0.0398085 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063764 | TAGGAAATATAAACA[-/C]CCCGCCCTCTCCCTT | 79734 |
rs531824792 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063289 | GAGAGTGGGTATGGC[A/G]GCTGAGCCAGGGGCC | 79734 |
rs531917277 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057248 | GAGCAGGTGCTCAGA[C/G]CATGGCTGCCTCCCC | 79734 |
rs531919529 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051464 | AAAACAAGAATGCTC[A/G]GACCCATGGGATGAC | 79734 |
rs532335419 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050407 | ACCGCACCCAGCCTA[C/T]GCTAGATGTTTATAG | 79734 |
rs532347604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055596 | TCGCTTCACTGGTGG[A/G]CTGACTTCTTCATCT | 79734 |
rs532421011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060459 | GGCTTCCTTGGCCAC[A/G]TTTCTACTGAGGAGC | 79734 |
rs532452879 | snp | A/G | 0.00017073 | 0.00923774 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056424 | CAGGTCGGGAGCAGG[A/G]GCAGCACACACGGCC | 79734 |
rs533100169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054558 | GGCTCATCCAGGGGA[C/T]AGGGGATCTGAGAGG | 79734 |
rs533531232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052194 | TCTCCAGCCGCCCCG[C/G]ATCGGGGCCTCTCCT | 79734 |
rs533725861 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056474 | AGAGAGAGGCTGAGA[C/G]ACGGGGCGGGAAGCA | 79734 |
rs533727767 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062883 | GCTCCTTCCTGGCCC[C/G]GTCACATTGCCTCCT | 79734 |
rs533796072 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051530 | GGCCGGGAGTTCGAC[A/C]TTCCCCATACACAGT | 79734 |
rs533804075 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062320 | CCCTTGCTGCTCCCC[C/G]CAACTCAGTTCTGAA | 79734 |
rs534402429 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049879 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAATGC | 79734 |
rs534440131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055845 | AAGCTGCTTCTCTTT[C/G]GGAGCCTCAGTTTTC | 79734 |
rs534467326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061314 | TGGTCCCAGCCTCCC[A/G]TGCCCTCCACCCAGG | 79734 |
rs534591158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060661 | CCAAGCTGCCCAGGG[A/G]ACCGGAGAAGATGCC | 79734 |
rs534746000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054380 | GCTGTCTGGGGGCTA[A/G]AGGATCAGACAGGGT | 79734 |
rs535018315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054701 | TAAAAGGAGTTAATA[G/T]TGCAGCATGGAGCTC | 79734 |
rs535130674 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058753 | TGAGAGCCTCTGGGT[A/G/T]TCTTTGGCAATTGCA | 79734 |
rs535289048 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052832 | ACTCAGACATCCTCT[A/C]ACCGGATGCTCACAG | 79734 |
rs535326241 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058111 | CCTCCCACCTTTCAG[G/T]TTTCCAGAGGAGCAG | 79734 |
rs535675385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052410 | GAAGGAGCGTTGGCC[A/C]AGCGGGCACTATTTC | 79734 |
rs535714919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057572 | AGGCCCCTCCCTTCC[C/T]GCAGCCCCAGCCTTG | 79734 |
rs535759512 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063616 | GCCGGGAGCCAGAAA[A/C]CAGAACTCTAGGGAG | 79734 |
rs535866124 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056806 | GCAAATTGTGCCTTT[C/T]GTGGCATCAGATGGT | 79734 |
rs536032999 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054728 | GCTCAGTTCCTGGCC[A/G]GAGGATGTGGGATGC | 79734 |
rs536115162 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051516 | ATTCTTTTCCCAGAG[C/G]CCGGGAGTTCGACCT | 79734 |
rs536277554 | snp | C/G | 1.70499e-05 | 0.0029197 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056422 | CCCAGGTCGGGAGCA[C/G]GGGCAGCACACACGG | 79734 |
rs536314471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062098 | CTTGGGCAAGTCACT[A/G]TCCCTCTCTGGGCCA | 79734 |
rs536849583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055188 | CGGTCCTCCTCTATC[A/G]GGGGTGGTCGCCCCC | 79734 |
rs537299318 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054299 | CACCCCAGCTGCGTC[A/G]CAGCCAGCACCTGTT | 79734 |
rs537437453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053802 | GGCCCTGGATATGCC[C/T]ATATCCGGGCCTAAC | 79734 |
rs537449317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059240 | CTTGATTTGAGTGCC[A/G]AGGTCTGTCGTATCC | 79734 |
rs537502952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052295 | GGGAAGGAGTCGACG[A/C]GGCTACTTCTCCCGC | 79734 |
rs537510296 | snp | C/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061672 | GGGGTGGAGCGAGGA[C/G]GGTGCTCATCTCTTG | 79734 |
rs537641981 | snp | C/T | 0.000103675 | 0.00719909 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057487 | TGATGGCTGGCGCTT[C/T]GAGCAGGTGCGCTGG | 79734 |
rs537678800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057067 | CCCTAAGCCCCACCC[A/G]TGTTCTTTCTTGAAT | 79734 |
rs538111249 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049918 | CAGGCGTGAGCCACC[A/G]GCTGTTTTTTGGTTT | 79734 |
rs538115970 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063035 | CAGCTGCCCTGGGAT[A/G]GGAAGGACCCAGCCC | 79734 |
rs538247734 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061961 | GAGGACAGGCCACTT[G/T]TGGATACCCTTGGCC | 79734 |
rs538334084 | snp | A/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059643 | CAGTGAAATGAGAGC[A/T]TCCCCAGGGTGCAGC | 79734 |
rs538494658 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057680 | GGTGGCAGGTTGACC[A/G]AGAGAGAGGATAGGA | 79734 |
rs538657756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061454 | CCCACTAACCCTGCC[A/G]GGCACCTCTGAGACT | 79734 |
rs538702606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054739 | GGCCGGAGGATGTGG[A/G]ATGCAGTGCTAGCTG | 79734 |
rs538704064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060769 | CCAGCAGGCCCTGGC[C/T]CCTCTGTTAGTGTCT | 79734 |
rs538840421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059736 | GACTAGGGGTCAGGG[C/T]ACAGTGTGGCACTCT | 79734 |
rs539272058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053720 | GTGCTGGCTGTGGGT[G/T]GAGGCAGGAGAGGGG | 79734 |
rs539318802 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062711 | TCCTGCCTCCAGGGG[C/T]GGGGCGGGGCCCCCC | 79734 |
rs539672462 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052961 | AGGTCCATCTGACCC[C/G]AGTGCCTTTTTGCTA | 79734 |
rs539695096 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058635 | CAGGGTCCCTGAGAG[C/T]TGAATGAGACTCATC | 79734 |
rs539832421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058204 | TTCTCCACGCCCACC[C/T]ACACGTTCCCTGGCA | 79734 |
rs540099425 | snp | A/C/T | 8.67009e-05 | 0.00658362 | intron-variant, missense, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061523 | CCGGCCTCCTCCTCA[A/C/T]GTTTCCTCCTTGCAG | 79734 |
rs540137583 | snp | C/T | 0.000498567 | 0.0157808 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061004 | AGCCAGCTGCAGAAC[C/T]GGGGGCCCCGGGGCT | 79734 |
rs540198226 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054513 | GGATCACGCAGGGCT[A/C]TCCGGGGGCTAGGGG | 79734 |
rs540290422 | in-del | -/GGGGCGGGAGCAGCGC | 0.0770498 | 0.180522 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051617 | AGCGGGGCGGGACCG[-/GGGGCGGGAGCAGCGC]GGGGCGGGAGCAGCG | 79734 |
rs541053621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059964 | CCTGCCCCTTTCCCA[C/G]GCCCCCTCCTTGGCT | 79734 |
rs541254320 | snp | A/C/G | 3.29582e-05 | 0.00405931 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053186 | TGGCAAGCTGGTGCT[A/C/G]GACAAGGACATGGCT | 79734 |
rs541291890 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058353 | TGCCACCTTGGGCAA[G/T]TTACATCTCCTGTGC | 79734 |
rs541327459 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063849 | GTTCCTTCAACTCCT[C/T]AGTCCTCCCCGCTGC | 79734 |
rs541488846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053827 | CCTAACAAACAGTGG[A/G]GAGGCCATGTCTGGG | 79734 |
rs541674812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057894 | GAGTCAGCATCATGC[A/G]ATCATAGCAGTTCCT | 79734 |
rs541695792 | snp | A/G | 0.000357334 | 0.0133619 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051868 | GGGCACGGTGTTCCT[A/G]ACCACCCGGCAGACG | 79734 |
rs541768733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057131 | GAGCTGGGTGACCTT[A/G]GGCAAGTAACTGGAC | 79734 |
rs542257182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056672 | CTCGCCCTCTCCGGA[A/C]CTTGATTTTCTCTTA | 79734 |
rs542542656 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060216 | CTCCTCCTGGGGCCC[A/G]ACCCCACACAGTGGA | 79734 |
rs542679954 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049985 | CAGGCGCAGTGGCTC[A/G]CACCTGTAATCCCAG | 79734 |
rs542856525 | snp | C/T | 0.000135437 | 0.00822801 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060972 | AAAGCCGGAGCCTCC[C/T]GCCCACTCCTTGCTG | 79734 |
rs543100263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059071 | CCCTCCACCAGGGAT[C/T]GGGCCAGCCAAGCCA | 79734 |
rs543212945 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055709 | TGTTGCAAACTGTAA[A/G]GTGAGGCAGTTGGGG | 79734 |
rs543313859 | snp | C/T | 0.000185377 | 0.0096257 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059427 | AGCTCAGAGTCCAGC[C/T]GCAAAACCAAGGTGA | 79734 |
rs543558047 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057794 | TGAGTGAGTCTGTGG[A/C]CCCCGAAGGACAGCT | 79734 |
rs543869217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058282 | GGGATGGAAGAATGG[C/G]CCTAGTGCAGAGCCA | 79734 |
rs543869395 | snp | A/G | 7.71992e-05 | 0.00621238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053079 | CACTCTTCTCTCACC[A/G]AGCATCCCTCACCTC | 79734 |
rs543907016 | snp | A/C | 0.000272926 | 0.0116785 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052627 | CTCAATGTCTCCGAT[A/C]TCTCTGTAGAGTCGC | 79734 |
rs543994826 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051647 | GCGGGGCGGGACCCT[A/T]CCCGCGGCCCACGCG | 79734 |
rs544035030 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051212 | AAATTCATAACACAT[A/G]TACACAAAGTGTCTG | 79734 |
rs544072072 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056631 | CAGTCCCTGTCTCAG[A/C]CCCATTTGCTGTGTG | 79734 |
rs544074551 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052793 | AGAGGGACATTCTTC[A/G]AGCCCTGTGCTGGGC | 79734 |
rs544074937 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057264 | CATGGCTGCCTCCCC[A/C]CAACCACCTCTTCTT | 79734 |
rs544109594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056109 | TCAGCACAGCAGAGC[G/T]GTGTGGCAGCCCCTC | 79734 |
rs544187968 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062425 | CCCTCTCCCCCACCC[A/G]TCAATCTCCTCTCCG | 79734 |
rs544307413 | snp | A/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059761 | CACTCTCTGTGTGAC[A/T]TAGGACAGGGCTTGT | 79734 |
rs544640111 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon, stop-gained, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061576 | ACCTGAGGCTGAGCT[A/T]GCAGTGAGGGCTTCT | 79734 |
rs544689231 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057915 | AGCAGTTCCTGACAC[A/G]GTTTTCAGGGTCTCC | 79734 |
rs545051789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055300 | AGCTAAATCAACCCT[A/G]GTGATCAGTGGAGTG | 79734 |
rs545091881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054964 | ATCAGAAATTTATTT[A/C]TCTTGGTCCTAGAGG | 79734 |
rs545128652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060079 | GCAGCATCCACTGTA[C/T]CACTGTGGGGAGAGG | 79734 |
rs545264966 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058869 | CTCTGCTTCCAGGAG[G/T]GAAGGGAATATTCTG | 79734 |
rs545299767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058382 | GCGGGACCCAGTTCC[C/T]TCATCGGTGAAGTGG | 79734 |
rs545867793 | snp | C/T | 0.000137278 | 0.00828372 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052607 | TTTGGCAAGTCGCCT[C/T]ACCTCTCAATGTCTC | 79734 |
rs546103285 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057016 | GGCTCCGTGTCTCCT[C/T]GAGGGCCTGACTCCT | 79734 |
rs546208305 | snp | G/T | 0.00538596 | 0.0516137 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051973 | CCCGGGGTGGGCGGC[G/T]AGCGGGCGGTGGGTC | 79734 |
rs546249793 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057689 | TTGACCGAGAGAGAG[A/G]ATAGGAGCCCCAGTG | 79734 |
rs546476295 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060485 | GGAGCAGTCTTTCCA[A/G]ACAAGGCCTTCCCAG | 79734 |
rs546633383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060337 | CTGACGCTGCCCTGC[A/C]AGGGTGCAGAGCGAG | 79734 |
rs547178191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053573 | GTGACAGGAATGCAG[C/T]GTTGACAGGCATGGG | 79734 |
rs547514728 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059144 | TGCAAGGGGGAAGAC[C/T]CCACCTTCCTGCCCA | 79734 |
rs547737139 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052184 | CATTAGAAGCTCTCC[A/C]GCCGCCCCGGATCGG | 79734 |
rs547856930 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062800 | TGGCAGATGTGTGGC[A/T]ATGTCTGGCTGTGTC | 79734 |
rs548206424 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056836 | TCGCCTGGTGGGCTC[A/G]GCACAGGCTGTTGGG | 79734 |
rs548227100 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050703 | CATTGGATCAGTGAG[A/G]GGAGCCCCAGACCTC | 79734 |
rs548241019 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049844 | CATGTTGGCCAGGCT[A/G]GTCTCGAACTCCTGA | 79734 |
rs548325824 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061850 | GCTGGTGGGGAGGGA[A/G]GGACCGCTGAAGCCA | 79734 |
rs548378289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056230 | GGCGGGTGATCAGAG[C/T]GAGAGGTGGGTTTCG | 79734 |
rs548396353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061704 | TCCTTGGACTTGAGC[C/T]GAGCTTTCGGCTGAT | 79734 |
rs548803912 | snp | C/T | 0.00024947 | 0.0111657 | synonymous-codon, intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061168 | TCCTCCTCCGCTTCC[C/T]GCTGGAGGTCCTGCC | 79734 |
rs548953415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054996 | TAGAAACCCGAGATC[A/G]GGGCACTGTGGCAGG | 79734 |
rs549245567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054691 | GTCATGAGGATAAAA[A/G]GAGTTAATAGTGCAG | 79734 |
rs549282598 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059692 | TACATGAAGGGGGCC[G/T]CTTAGTGGCCACTGG | 79734 |
rs549484167 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050341 | GGTCTTGAACTTCTA[G/T]GCTCAAGCGAGCCTT | 79734 |
rs550047865 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063570 | ATATCCTTTGCCCTG[C/G]GGCCGGATACCAGAG | 79734 |
rs550231152 | snp | C/G | 0.0138799 | 0.0821421 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062721 | AGGGGCGGGGCGGGG[C/G]CCCCCTGGGACCTCT | 79734 |
rs550305743 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052017 | ACGCGGGGCTGTCGG[G/T]CCTGGCTCGCCCGCC | 79734 |
rs550469328 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049774 | AGCTGGAACTACAGG[C/T]GTGAGCCACCATGCC | 79734 |
rs550482247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056759 | GTCAGTGTGGAGGTA[C/T]AGGGTGCCCTGCAGA | 79734 |
rs550513336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061983 | CCCTTGGCCCATGAA[A/G]TGTCAGCCAGAGTGG | 79734 |
rs550779251 | snp | A/G | 0.0007246 | 0.0190204 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061065 | CTTGCCTGGCGCCTC[A/G]CCCGCATAACCATCC | 79734 |
rs550938464 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057792 | CATGAGTGAGTCTGT[A/G]GCCCCCGAAGGACAG | 79734 |
rs551073058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060535 | CAGTCCCACACCCTC[C/T]CTGTTCTGCTTCATC | 79734 |
rs551264105 | snp | C/G | 0.000538213 | 0.0163956 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052674 | CCTCCCTGCCCGCCC[C/G]AGTGTCCAGTGAGAT | 79734 |
rs551685338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059204 | CCCGACAAGCCGCAA[C/G]ATTAGGACCTGAGCT | 79734 |
rs551718642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058637 | GGGTCCCTGAGAGCT[A/G]AATGAGACTCATCAC | 79734 |
rs552040279 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061468 | CGGGCACCTCTGAGA[C/T]TGGGCCCTGGCTGCA | 79734 |
rs552243696 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057860 | GAGTCCACATTGAGT[C/G]AGTACCTCTTAGAAC | 79734 |
rs552646345 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050842 | GCTCCCTTCCCCCAT[C/T]CTGAGGTCCACAGAA | 79734 |
rs552711152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056715 | GGGTGGGAATGGCAC[A/G]CCCATCCCTTCCTCA | 79734 |
rs552919951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061354 | CCTGCATCCCAGAGC[A/G]TCCTGCCTGCCGCCT | 79734 |
rs552962950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060736 | TCACCTTGCCTGAGA[C/G]CGGGTCTTTGGGGAT | 79734 |
rs553067785 | snp | C/G | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059332 | TGAACATCGGCTCCT[C/G]CTACAACTACGGCAG | 79734 |
rs553104705 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058775 | GCAATTGCACAGGCT[C/T]TCAGAGGCTGAGCAA | 79734 |
rs553209558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053834 | AACAGTGGGGAGGCC[A/G]TGTCTGGGAGAACGA | 79734 |
rs553412984 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054403 | GACAGGGTTATCTGG[A/G]GGCTAGGGGATCACA | 79734 |
rs554299766 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063199 | CATTGCTGGCCCAGC[A/G]CCTGGCCTGGGGGGC | 79734 |
rs554419191 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051155 | TCATCTGTAAAATGG[G/T]TATAGCCCAAAATAC | 79734 |
rs554666980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056067 | GCCCCAGACGGTGGC[C/T]TGGCAGGTACCCCTG | 79734 |
rs554904642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055191 | TCCTCCTCTATCGGG[A/G]GTGGTCGCCCCCTTC | 79734 |
rs554941400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060637 | TCAGCTGCTTTCCCC[A/C]GGCCCTCCCCAAGCT | 79734 |
rs555256863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059877 | GGGATCCCAAATGGC[C/T]GTTTATTCCCCAGGG | 79734 |
rs555808406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058734 | AACAAGGGCAGGGCC[A/G]CTCTGAGAGCCTCTG | 79734 |
rs555836684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053804 | CCCTGGATATGCCCA[C/T]ATCCGGGCCTAACAA | 79734 |
rs555873447 | snp | A/G | 0.000108307 | 0.00735811 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053111 | ATAGGATGAGACCGG[A/G]GCCTACCTCATTGAC | 79734 |
rs555901657 | snp | G/T | 0.00242424 | 0.034731 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051802 | GCCGCCGGCGGGGGC[G/T]GGCGGCCGCGCCGCA | 79734 |
rs556219268 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063050 | GGGAAGGACCCAGCC[C/T]GACCCCTGGGCATAA | 79734 |
rs556433011 | in-del | -/AG | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056629 | TTCAGTCCCTGTCTC[-/AG]CCCCATTTGCTGTGT | 79734 |
rs556474244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062440 | GTCAATCTCCTCTCC[A/G]CCCCCTTGCCCTGCA | 79734 |
rs556918524 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049919 | AGGCGTGAGCCACCG[A/G]CTGTTTTTTGGTTTT | 79734 |
rs556959249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055984 | AGGGGTCAGGCAAGG[C/T]CCTGCTCATGGTGAC | 79734 |
rs557054290 | snp | C/G | 0 | 0 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060834 | ACAGAGCACGGAGGA[C/G]CAGCTGGAGGAGCAG | 79734 |
rs557054645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054775 | CACCTGCAGGGCTCC[A/G]CCCAGGGCACTGGGG | 79734 |
rs557089241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059754 | AGTGTGGCACTCTCT[A/G]TGTGACTTAGGACAG | 79734 |
rs557230272 | snp | A/G | 5.00647e-05 | 0.00500298 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059406 | CACAGCACCCCAAAC[A/G]GGCTGAGCTCAGAGT | 79734 |
rs557685250 | in-del | -/CTT | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055601 | TCACTGGTGGGCTGA[-/CTT]CTTCATCTCCCAGAT | 79734 |
rs558002507 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063673 | TAAACCTCTCAGCGC[A/G]CCCCCTCCACTTCTA | 79734 |
rs558066003 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053726 | GCTGTGGGTGGAGGC[A/G]GGAGAGGGGGGAGTC | 79734 |
rs558278534 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057731 | GCACGGGGTGTCCTT[G/T]TTGGTGGGAGTCCTC | 79734 |
rs558289308 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062923 | GTCCAGGGGGTCACT[C/T]CTCCCACCCCACCTA | 79734 |
rs558351477 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051575 | GCATCTTCACCACCC[C/G]AGACTGCGGGCCTGC | 79734 |
rs558841460 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063215 | CCTGGCCTGGGGGGC[A/G]GGGAGAGGCAGCAGA | 79734 |
rs558927384 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049880 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAATGCT | 79734 |
rs559393631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054553 | GCTAGGGCTCATCCA[A/G]GGGATAGGGGATCTG | 79734 |
rs559405640 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057045 | CTTGAGGGTGACCCA[A/G]AATGTTCCCTAAGCC | 79734 |
rs559523867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059508 | CTCCCCGCCTGTCCC[A/G]CCCCTGCGCCTGCAC | 79734 |
rs560231636 | snp | A/G | 0.00286181 | 0.0377189 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061060 | AGCCACTTGCCTGGC[A/G]CCTCACCCGCATAAC | 79734 |
rs560412250 | snp | C/G | 0.00199481 | 0.0315187 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051871 | CACGGTGTTCCTGAC[C/G]ACCCGGCAGACGCTG | 79734 |
rs560635803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | KCTD17 | GRCh38.p7 | 22:37061723 | CTTTCGGCTGATTAT[C/T]TCCACCCACCAAAGT | 79734 |
rs561019135 | snp | C/T | 0.000262329 | 0.0114497 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060978 | GGAGCCTCCCGCCCA[C/T]TCCTTGCTGGAGCCA | 79734 |
rs561266037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060303 | CCTGCCTGCCCACCC[A/T]CCCCCACCACTGCCA | 79734 |
rs561437860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054476 | AGGCTAGGGGATCAC[A/G]CAGGGCTATCCGGGG | 79734 |
rs561677304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054111 | GAGCCCTATGGGACA[C/T]AGTGGTCTGGAGGCC | 79734 |
rs562494938 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056217 | AGCTCACCCTCAGGG[C/T]GGGTGATCAGAGCGA | 79734 |
rs562583922 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058634 | CAGGGTCCCTGAGAG[-/T]CTGAATGAGACTCAT | 79734 |
rs562875717 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060383 | TCTTTGGGCCAAAGC[A/C]CCTGGACCTGGGGTG | 79734 |
rs563025506 | snp | A/C | 0.00116618 | 0.0241191 | missense, intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061127 | TCTCAGGATCCCGCT[A/C]ACCTTTTCTCCCTCC | 79734 |
rs563310250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060113 | GAGCGGGGGTCCTGC[C/T]ATCCTGGACCCAGTG | 79734 |
rs563508236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059660 | CCCCAGGGTGCAGCC[A/G]GCGTGGACTCAGAGG | 79734 |
rs563636622 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053922 | TCTTTGGGACACAGG[G/T]TGTGGCTCTGGGTCA | 79734 |
rs563711604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058387 | ACCCAGTTCCCTCAT[C/T]GGTGAAGTGGGCTAA | 79734 |
rs563881604 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049978 | TGGGGGCCAGGCGCA[G/T]TGGCTCGCACCTGTA | 79734 |
rs564008899 | in-del | -/TCCCTCCACTCTCCT | 0.00478085 | 0.0486577 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053008 | TCCAGGGAAGAGCTC[-/TCCCTCCACTCTCCT]TCCCTCCCTGTGCGT | 79734 |
rs564421158 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051979 | GTGGGCGGCGAGCGG[G/T]CGGTGGGTCCTCCGC | 79734 |
rs564644826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056716 | GGTGGGAATGGCACA[C/T]CCATCCCTTCCTCAT | 79734 |
rs564644935 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063270 | GACTCAGGAACTGCC[C/T]GGGGAGAGTGGGTAT | 79734 |
rs564681008 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062655 | GAAGAAGCACCCTCT[A/C]CCCGGCCTCCTCTGT | 79734 |
rs564944796 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054599 | GCTGTGTGACACTGA[A/G]AAAGTGACCTAACCC | 79734 |
rs565671883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054157 | AGGTCAGGGCCACAA[C/T]ACCAGAGTCCACTGT | 79734 |
rs565744825 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052922 | TCACACATTCAGGAA[G/T]AGTCAGAAGCAGGGC | 79734 |
rs565839364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053608 | GCTCTGTCTCTCTTT[C/T]TCTGGCTGATCCAGT | 79734 |
rs566023962 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058197 | CTAGCCTTTCTCCAC[A/G]CCCACCCACACGTTC | 79734 |
rs566351841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056858 | GCTGTTGGGGCTGGC[A/G]TTTGTGACCTTGGAG | 79734 |
rs566884924 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049877 | TTGTGATCTGCCTGC[C/T]TCGGCCTCCCAAAAT | 79734 |
rs566922361 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055726 | TGAGGCAGTTGGGGG[A/T]ATGCATGGACACAAG | 79734 |
rs567062422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055224 | TGGAGCTCACAGCTT[C/T]GGGAGGGACACACCT | 79734 |
rs567079080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061313 | CTGGTCCCAGCCTCC[C/T]GTGCCCTCCACCCAG | 79734 |
rs567198769 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060646 | TTCCCCAGGCCCTCC[A/C]CAAGCTGCCCAGGGG | 79734 |
rs567807295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053458 | GTGCAGGGGATAGAG[A/G]AAGTCAGCGAGGCCC | 79734 |
rs568166316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057556 | TAGCCTCTGACCAAG[A/C]AGGCCCCTCCCTTCC | 79734 |
rs568305999 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063583 | TGGGGCCGGATACCA[C/G]AGCACCTGCCCTACC | 79734 |
rs568765574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062044 | CTGGCCATGTGCCCA[C/T]AAGCCCCCTATCCCA | 79734 |
rs568799442 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062731 | CGGGGCCCCCCTGGG[A/C]CCTCTTAAGGCCCAA | 79734 |
rs568862637 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049790 | GTGAGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 79734 |
rs568906504 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057930 | AGTTTTCAGGGTCTC[C/T]GCAGGGGACATGCCC | 79734 |
rs569000487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055606 | GGTGGGCTGACTTCT[C/T]CATCTCCCAGATTAA | 79734 |
rs569035212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055185 | GTCCGGTCCTCCTCT[A/G]TCGGGGGTGGTCGCC | 79734 |
rs569043876 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061486 | GGCCCTGGCTGCAGG[C/T]CCTGCCCCCCCTCCT | 79734 |
rs569293950 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058607 | AGGCCTTCAGCAGGC[C/G]TGAGATTCTCTTCAG | 79734 |
rs569316304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060595 | GCAGCCAGGCTGACC[C/G]CGGAGCATGCCCACA | 79734 |
rs569434734 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059769 | GTGTGACTTAGGACA[A/G]GGCTTGTCCTCTCCC | 79734 |
rs569954130 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054294 | GTAAACACCCCAGCT[G/T]CGTCGCAGCCAGCAC | 79734 |
rs569991010 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053733 | GTGGAGGCAGGAGAG[C/G/T]GGGGAGTCTGCTTCC | 79734 |
rs570032076 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058692 | GCCAGAAGGGCTCTG[A/T]GGGCGTGGTTATTCT | 79734 |
rs570089719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052666 | CCACCCTGCCTCCCT[A/G]CCCGCCCGAGTGTCC | 79734 |
rs570929529 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050903 | TAACTCAGAAAGCCA[C/T]CCGCAGAACCAATCC | 79734 |
rs571095816 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052837 | GACATCCTCTCACCG[A/G]ATGCTCACAGCAAAC | 79734 |
rs571209932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055907 | TCCTTCTAGTTCTGA[A/G]AATTCAAAAATGTAA | 79734 |
rs571281903 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055089 | AGAAAGAGAGGGAGC[C/T]AGCCCTCGCCCGCCC | 79734 |
rs571319534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060428 | GCATCCCAGATCTGG[A/G]TGGTGTCTGCCCTGG | 79734 |
rs571457454 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059706 | CGCTTAGTGGCCACT[A/G]GGCACTGTGGCATGG | 79734 |
rs571627816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054738 | TGGCCGGAGGATGTG[G/T]GATGCAGTGCTAGCT | 79734 |
rs571685472 | in-del | -/ACC | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061809 | AGTGGGAACTTTCCT[-/ACC]ACCAGCCCATCAGCA | 79734 |
rs572333922 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051904 | CCGCGAGCAGAAGTC[C/T]TTCCTCAGCCGCCTG | 79734 |
rs572353542 | snp | A/C/T | 0.000279769 | 0.0118246 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052546 | GGTCTGAAGATGACC[A/C/T]CTAAGGTCTCCTGTC | 79734 |
rs572373930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057146 | GGGCAAGTAACTGGA[C/G]CTCTCTGAGCCTCAA | 79734 |
rs572457840 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057684 | GCAGGTTGACCGAGA[C/G]AGAGGATAGGAGCCC | 79734 |
rs572496486 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063637 | CTCTAGGGAGAGCCC[C/T]GGGCTGCCTCTGCCA | 79734 |
rs572534859 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063214 | GCCTGGCCTGGGGGG[C/T]GGGGAGAGGCAGCAG | 79734 |
rs572719784 | snp | A/G | 0.000145705 | 0.00853413 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061510 | CCCTCCTCTCCTCCC[A/G]GCCTCCTCCTCACGT | 79734 |
rs572763085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060981 | GCCTCCCGCCCACTC[C/T]TTGCTGGAGCCAGCT | 79734 |
rs572822016 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054490 | CACAGGGCTATCCGG[A/G]GGCTAGGGGATCACG | 79734 |
rs572934396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056077 | GTGGCCTGGCAGGTA[C/T]CCCTGGGTCACCGCA | 79734 |
rs573293088 | in-del | -/CTGGCCCAGCGC | 0.0023933 | 0.0345097 | cds-indel, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063189 | CAGCCATTTGCATTG[-/CTGGCCCAGCGC]CTGGCCTGGGGGGCG | 79734 |
rs573566186 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD17 | GRCh38.p7 | 22:37054487 | TCACACAGGGCTATC[C/T]GGGGGCTAGGGGATC | 79734 |
rs573956574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053808 | GGATATGCCCATATC[C/T]GGGCCTAACAAACAG | 79734 |
rs574092484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058741 | GCAGGGCCACTCTGA[A/G]AGCCTCTGGGTGTCT | 79734 |
rs574123241 | snp | C/T | 4.23433e-05 | 0.00460107 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053129 | CTACCTCATTGACCG[C/T]GACCCCACCTACTTC | 79734 |
rs574161397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058342 | ACAGACATGCCTGCC[A/G]CCTTGGGCAAGTTAC | 79734 |
rs574514694 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050434 | ATAGACATTTCATAA[C/G]TTAATCTTCACAGCA | 79734 |
rs574579704 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055593 | TCATCGCTTCACTGG[C/T]GGGCTGACTTCTTCA | 79734 |
rs574717152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057127 | CCTTGAGCTGGGTGA[A/C]CTTGGGCAAGTAACT | 79734 |
rs575317477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056060 | TAAAGCTGCCCCAGA[C/T]GGTGGCCTGGCAGGT | 79734 |
rs575326144 | snp | C/T | 0.000135621 | 0.00823359 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060971 | CAAAGCCGGAGCCTC[C/T]CGCCCACTCCTTGCT | 79734 |
rs575339586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, stop-gained, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061477 | CTGAGACTGGGCCCT[A/G]GCTGCAGGCCCTGCC | 79734 |
rs575891732 | snp | C/G | 1.6701e-05 | 0.00288968 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059408 | CAGCACCCCAAACGG[C/G]CTGAGCTCAGAGTCC | 79734 |
rs575972841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059009 | AAGGGCCCCCTGGCT[C/G]TGGGGCTAGGCTGGA | 79734 |
rs576507940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052625 | CTCTCAATGTCTCCG[A/G]TCTCTCTGTAGAGTC | 79734 |
rs576555295 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051638 | GGGAGCAGCGCGGGG[A/C]GGGACCCTACCCGCG | 79734 |
rs576649422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057775 | GGTGATCTATCTGGT[A/G]GCATGAGTGAGTCTG | 79734 |
rs576802068 | snp | C/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061569 | CTCTCAGACCTGAGG[C/G]TGAGCTTGCAGTGAG | 79734 |
rs577077531 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060172 | AGCCACAGAGCAGGC[A/G]TGAACCAGGCTGGGA | 79734 |
rs577107502 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062362 | TGGGCCTCAGCCCCA[C/G]CCCCTCCTCCAGAAG | 79734 |
rs577281266 | in-del | -/T | 0.0115144 | 0.0749975 | utr-variant-3-prime, downstream-variant-500B, frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062727 | GGGGCGGGGCCCCCC[-/T]GGGACCTCTTAAGGC | 79734 |
rs577380955 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049890 | GCCTCGGCCTCCCAA[A/G]ATGCTAGGATTACAG | 79734 |
rs577697341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37055297 | ATCAGCTAAATCAAC[C/T]CTGGTGATCAGTGGA | 79734 |
rs577803443 | snp | C/G/T | 8.2931e-05 | 0.0064389 | missense, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059348 | CTACAACTACGGCAG[C/G/T]GAGGACCAGGCAGAG | 79734 |
rs577853408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060028 | AGTCCTGTGTGTCCG[C/T]CTGGCCTGTTGAGGC | 79734 |
rs577877181 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KCTD17 | GRCh38.p7 | 22:37058381 | TGCGGGACCCAGTTC[C/G]CTCATCGGTGAAGTG | 79734 |
rs578113654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053844 | AGGCCATGTCTGGGA[A/G]AACGACCTGTTAGCA | 79734 |
rs745519858 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050861 | AGGTCCACAGAATGA[C/T]GGTTCCCCTCCGAGT | 79734 |
rs745616930 | in-del | -/GAG | | | intron-variant, cds-indel | KCTD17 | GRCh38.p7 | 22:37061776 | GGGGTGAGGCTCTGA[-/GAG]GAGAAGAAAGTTAGG | 79734 |
rs745692024 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056783 | CTGCAGAGGAAAATG[C/T]AGGATTAGCAAATTG | 79734 |
rs745801740 | snp | G/T | 1.74296e-05 | 0.00295204 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062550 | CCAGAGGCACCCGGA[G/T]GTGAGGCCCCAGATC | 79734 |
rs745853104 | snp | A/C | 2.60875e-05 | 0.00361152 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062490 | CCCACCTCCGCCCCT[A/C]CCATCCTCCTGCCCT | 79734 |
rs745889631 | snp | A/C | 3.35869e-05 | 0.00409784 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056372 | GCTGATCCGCATCAT[A/C]AAAGACCGGATGGAA | 79734 |
rs746122376 | snp | C/T | 3.53195e-05 | 0.0042022 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056454 | CAGGGCAGGGGCCAG[C/T]GGGGAGAGAGAGGCT | 79734 |
rs746150184 | snp | A/G | 0.00013987 | 0.00836154 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060944 | CCAACCCCCAGGAGG[A/G]TGATTGCTAAGCAAA | 79734 |
rs746274419 | in-del | -/G | 1.73939e-05 | 0.00294901 | frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057493 | CTGGCGCTTCGAGCA[-/G]GTGCGCTGGGGACAG | 79734 |
rs746352966 | snp | A/G | 0.000165003 | 0.00908153 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051895 | GACGCTGTGCCGCGA[A/G]CAGAAGTCCTTCCTC | 79734 |
rs746388490 | in-del | -/C | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049836 | GTTTCACCATGTTGG[-/C]CCAGGCTGGTCTCGA | 79734 |
rs746408279 | snp | G/T | 0.000124914 | 0.00790199 | intron-variant, missense, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061223 | TCCTGGATCTCATCT[G/T]CACCCTGCCTCTTCC | 79734 |
rs746481136 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058047 | AGATGCAGTTTACCC[A/G]TCGGGAGATCCTTAT | 79734 |
rs746524755 | snp | A/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056076 | GGTGGCCTGGCAGGT[A/T]CCCCTGGGTCACCGC | 79734 |
rs746534079 | snp | A/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059560 | CCACCGCCCATGCAC[A/T]ACCCCATGCTCACAG | 79734 |
rs746652573 | snp | A/G | 1.83075e-05 | 0.00302546 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057509 | GTGCGCTGGGGACAG[A/G]GGCGTGCCACCAGGA | 79734 |
rs746742716 | snp | C/T | 1.65902e-05 | 0.00288008 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059323 | TCTAGCTGGTGAACA[C/T]CGGCTCCTCCTACAA | 79734 |
rs746903628 | snp | C/T | 7.90186e-05 | 0.00628515 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061595 | GTGAGGGCTTCTCCT[C/T]GGCCCCTCGCCCGCC | 79734 |
rs747042008 | snp | C/T | 2.77496e-05 | 0.00372479 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062483 | TACCGGCCCCACCTC[C/T]GCCCCTCCCATCCTC | 79734 |
rs747167411 | snp | C/T | 3.36751e-05 | 0.00410322 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056364 | ATCGGCCCGCTGATC[C/T]GCATCATCAAAGACC | 79734 |
rs747215623 | snp | G/T | 1.69499e-05 | 0.00291112 | splice-donor-variant | KCTD17 | GRCh38.p7 | 22:37056412 | TACACGGTCACCCAG[G/T]TCGGGAGCAGGGGCA | 79734 |
rs747411979 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052964 | TCCATCTGACCCCAG[C/T]GCCTTTTTGCTACTT | 79734 |
rs747506125 | snp | A/G | 3.85765e-05 | 0.00439167 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060868 | CAGCAGGAGGAGGAG[A/G]TGGAGGAGGTGGAGG | 79734 |
rs747561124 | snp | A/G | 3.3749e-05 | 0.00410772 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059428 | GCTCAGAGTCCAGCC[A/G]CAAAACCAAGGTGAG | 79734 |
rs747702083 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053785 | CAGGCCTAGGTGGCC[A/G]AGGCCCTGGATATGC | 79734 |
rs747826376 | snp | A/G | 0.000185856 | 0.00963813 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051859 | CAACGTGGGGGGCAC[A/G]GTGTTCCTGACCACC | 79734 |
rs747922184 | snp | C/G | 2.06473e-05 | 0.00321298 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057356 | CTCCTGGGGTGCCTG[C/G]TGCTCCCACAGGTGC | 79734 |
rs748291483 | snp | A/G | 4.76156e-05 | 0.00487909 | intron-variant, synonymous-codon | KCTD17 | GRCh38.p7 | 22:37061669 | GGAGGGGTGGAGCGA[A/G]GAGGGTGCTCATCTC | 79734 |
rs748353168 | snp | C/G/T | 0.000240671 | 0.0109675 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053073 | AAGCCTCACTCTTCT[C/G/T]TCACCGAGCATCCCT | 79734 |
rs748421193 | in-del | -/CC | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051303 | GGGAAAGAACCCACT[-/CC]CACCCACCCCGCCCC | 79734 |
rs748584295 | snp | A/C | 6.39611e-05 | 0.00565477 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053176 | TCCTCCGGCATGGCA[A/C]GCTGGTGCTGGACAA | 79734 |
rs748704837 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054159 | GTCAGGGCCACAACA[C/T]CAGAGTCCACTGTAG | 79734 |
rs748740845 | snp | C/T | 3.34745e-05 | 0.00409098 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059414 | CCCAAACGGGCTGAG[C/T]TCAGAGTCCAGCCGC | 79734 |
rs748975595 | snp | C/T | 0.00172659 | 0.0293311 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059487 | AGTCTCCTGTCTCCC[C/T]CCACCCTCCCCGCCT | 79734 |
rs749046876 | snp | G/T | 3.68012e-05 | 0.00428944 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062581 | ACCTCCAGGGACTTG[G/T]GGTTCCCATCTGAAA | 79734 |
rs749086265 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060659 | CCCCAAGCTGCCCAG[A/G]GGACCGGAGAAGATG | 79734 |
rs749246602 | snp | A/C | 1.67944e-05 | 0.00289775 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056386 | TCAAAGACCGGATGG[A/C]AGAGAAGGACTACAC | 79734 |
rs749261230 | in-del | -/CT | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062398 | CTGTGACTCAACTGC[-/CT]CTCTCTCTCTCCCTC | 79734 |
rs749339217 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053340 | CTCTTCCCAGTCGGA[C/T]GGGGCTGATTCCCAA | 79734 |
rs749481891 | in-del | -/GAGCC | 1.70365e-05 | 0.00291855 | splice-donor-variant | KCTD17 | GRCh38.p7 | 22:37059440 | CCGCAAAACCAAGGT[-/GAGCC]GAGCCCACCCGCCTC | 79734 |
rs749559654 | snp | A/T | 2.57251e-05 | 0.00358635 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051965 | GTGAGGCCCCCGGGG[A/T]GGGCGGCGAGCGGGC | 79734 |
rs749969214 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053965 | AGACCAGCTTGAATA[C/T]GTCACTTCTCCTCAC | 79734 |
rs750023360 | snp | C/G | 0.000286672 | 0.0119689 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056320 | TTCTGTCTGTGCCAG[C/G]GGTCCTGGAGGAAGC | 79734 |
rs750244982 | snp | C/T | 1.85844e-05 | 0.00304826 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059481 | CGGAGAAGTCTCCTG[C/T]CTCCCTCCACCCTCC | 79734 |
rs750258810 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060220 | TCCTGGGGCCCAACC[C/G]CACACAGTGGAGGCT | 79734 |
rs750621399 | snp | A/G | 1.66228e-05 | 0.0028829 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057451 | GGAGGAGGAGCTCAC[A/G]CAAATGGTCTCCACC | 79734 |
rs750625624 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057686 | AGGTTGACCGAGAGA[A/G]AGGATAGGAGCCCCA | 79734 |
rs750863047 | snp | G/T | 1.97046e-05 | 0.00313878 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061534 | CTCACGTTTCCTCCT[G/T]GCAGGTTCCCGTCCG | 79734 |
rs751146810 | in-del | -/T | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062512 | CCTGCCCTTCCCCTC[-/T]TTTTTTTTCTAGCTG | 79734 |
rs751163807 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054033 | TCTGCCTTCTGGAGG[A/G]AGATGTCATAAATCC | 79734 |
rs751230786 | snp | C/T | 7.4011e-05 | 0.00608277 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053141 | CCGTGACCCCACCTA[C/T]TTCGGGCCCATCCTG | 79734 |
rs751269941 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054735 | TCCTGGCCGGAGGAT[G/T]TGGGATGCAGTGCTA | 79734 |
rs751540747 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060597 | AGCCAGGCTGACCCC[A/G]GAGCATGCCCACAGC | 79734 |
rs751577612 | snp | A/G | 1.66726e-05 | 0.00288722 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059403 | CTCCACAGCACCCCA[A/G]ACGGGCTGAGCTCAG | 79734 |
rs751583833 | snp | A/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061788 | TGAGAGGAGAAGAAA[A/G]TTAGGGAGTGGGAAC | 79734 |
rs751660189 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058255 | AGGTCGGAGCCCCCA[A/G]GATGGCCTGGAGGGA | 79734 |
rs751748057 | snp | A/G | 1.65523e-05 | 0.00287678 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062644 | GGCCTGAGAAGGAAG[A/G]AGCACCCTCTCCCCG | 79734 |
rs752012072 | snp | C/T | 4.96742e-05 | 0.00498344 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057421 | CAAGCACGTGTACCG[C/T]GTGCTGCAGTGCCAG | 79734 |
rs752103330 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059499 | CCCTCCACCCTCCCC[A/G]CCTGTCCCGCCCCTG | 79734 |
rs752142758 | snp | C/T | 0.000248602 | 0.0111463 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061161 | CACTGCCTCCTCCTC[C/T]GCTTCCCGCTGGAGG | 79734 |
rs752263327 | snp | A/C | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37061925 | CTGCCTTGTGGCATC[A/C]CCTATTTCTGTGGGG | 79734 |
rs752297218 | in-del | -/C | 2.33163e-05 | 0.00341432 | frameshift-variant, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061625 | CCCCAGAGCTGCCAT[-/C]CCTGGTTTGTAGCTT | 79734 |
rs752331716 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055786 | CTCTGGAGTCTGCAG[C/T]GCTTGAGTTCCCTCT | 79734 |
rs752376156 | snp | C/T | 2.0998e-05 | 0.00324015 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061526 | GCCTCCTCCTCACGT[C/T]TCCTCCTTGCAGGTT | 79734 |
rs752565743 | snp | A/C | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051334 | CCACCCCTATACACA[A/C]AAAGGGCAAATGAAA | 79734 |
rs752624522 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050566 | AGGATTCCAGTACAC[C/T]TTTGATCCACTCCCT | 79734 |
rs752645202 | snp | A/G | 6.64408e-05 | 0.00576333 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059303 | TTCTCCCCATGCTCC[A/G]CCCCTCTAGCTGGTG | 79734 |
rs752773805 | snp | G/T | 1.66233e-05 | 0.00288295 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059389 | TGGTGTCCAAGGAGC[G/T]CCACAGCACCCCAAA | 79734 |
rs752912726 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060027 | CAGTCCTGTGTGTCC[A/G]CCTGGCCTGTTGAGG | 79734 |
rs753280846 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063115 | GATGCAGGTTGTGGG[C/G]AGCTGGCCTGGCAGA | 79734 |
rs753453778 | snp | A/G | 0.000208464 | 0.0102073 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061069 | CCTGGCGCCTCACCC[A/G]CATAACCATCCCTTC | 79734 |
rs753632361 | snp | C/T | 0.000301386 | 0.012272 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051795 | AGGCAGCGCCGCCGG[C/T]GGGGGCGGGCGGCCG | 79734 |
rs754015064 | snp | A/G | 3.32331e-05 | 0.0040762 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059296 | TGCATTTTTCTCCCC[A/G]TGCTCCGCCCCTCTA | 79734 |
rs754048710 | snp | A/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061748 | CAAAGTTTCTCATCC[A/G]ACCTTGGCCTTGGGG | 79734 |
rs754143299 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058439 | CTTGTGAGATTAGAA[A/G]GGCCATCAGTAAAGC | 79734 |
rs754259514 | in-del | -/CT | 0.000432103 | 0.0146923 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062510 | CCTCCTGCCCTTCCC[-/CT]CTTTTTTTTCTAGCT | 79734 |
rs754371968 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055690 | GTGATGAGCTCGTGC[A/G]GGGTGTTGCAAACTG | 79734 |
rs754379400 | snp | C/T | 1.7698e-05 | 0.00297468 | missense, utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062535 | TCTAGCTGTTACAAG[C/T]CAGAGGCACCCGGAT | 79734 |
rs754393971 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055055 | AGACTGCTGACTTCT[C/T]GTTGTGTCCTCACAT | 79734 |
rs754430753 | snp | C/T | 2.79045e-05 | 0.00373517 | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061643 | TGGTTTGTAGCTTGG[C/T]GGTGCTGGAGGGAGG | 79734 |
rs754439410 | snp | A/G | 4.05688e-05 | 0.00450364 | synonymous-codon, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060828 | TGGTTCACAGAGCAC[A/G]GAGGAGCAGCTGGAG | 79734 |
rs754446980 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056119 | AGAGCTGTGTGGCAG[A/C]CCCTCAGCCCCTTCC | 79734 |
rs754992910 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058467 | AGCTTACAGCCCTCC[A/G]TAGGACTCCCTATGT | 79734 |
rs755029917 | snp | A/G | 1.72847e-05 | 0.00293974 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057488 | GATGGCTGGCGCTTC[A/G]AGCAGGTGCGCTGGG | 79734 |
rs755223753 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057561 | TCTGACCAAGCAGGC[C/T]CCTCCCTTCCTGCAG | 79734 |
rs755228334 | snp | A/G | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053145 | GACCCCACCTACTTC[A/G]GGCCCATCCTGAACT | 79734 |
rs755377405 | in-del | -/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060387 | TGGGCCAAAGCCCCT[-/G]GACCTGGGGTGTCAG | 79734 |
rs755400870 | snp | C/T | 1.85855e-05 | 0.00304834 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061548 | TTGCAGGTTCCCGTC[C/T]GCACCCTCTCAGACC | 79734 |
rs755428400 | snp | A/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055866 | CTCAGTTTTCCCAGT[A/T]GTTCAATGCAGATGA | 79734 |
rs755532238 | snp | A/G | 0.000123115 | 0.00784489 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056327 | TGTGCCAGGGGTCCT[A/G]GAGGAAGCCGAGTTC | 79734 |
rs755585851 | snp | C/G | 1.7612e-05 | 0.00296744 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062538 | AGCTGTTACAAGCCA[C/G]AGGCACCCGGATGTG | 79734 |
rs755708041 | snp | C/T | | | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063424 | TTCTCTGGGCCACTT[C/T]TGGGGACGGGGCTAA | 79734 |
rs755790333 | snp | G/T | 1.67075e-05 | 0.00289023 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059410 | GCACCCCAAACGGGC[G/T]GAGCTCAGAGTCCAG | 79734 |
rs755953955 | snp | C/G | 1.86263e-05 | 0.00305169 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059482 | GGAGAAGTCTCCTGT[C/G]TCCCTCCACCCTCCC | 79734 |
rs756139290 | snp | A/C/T | 0.000168132 | 0.00916734 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057334 | GTGGCAGCAGGTGCT[A/C/T]ATGCCCCTCCTGGGG | 79734 |
rs756513518 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052440 | CTGAGCACCCACCCT[A/G]ACTCTGCTGCACACT | 79734 |
rs756664045 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050793 | TTCCTCGTCAGCCCT[C/T]GTCCCTCCCTGGTCC | 79734 |
rs756682413 | snp | C/T | 0.000400357 | 0.0141428 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053144 | TGACCCCACCTACTT[C/T]GGGCCCATCCTGAAC | 79734 |
rs756711502 | snp | A/G | 1.91944e-05 | 0.00309788 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061539 | GTTTCCTCCTTGCAG[A/G]TTCCCGTCCGCACCC | 79734 |
rs756733390 | snp | C/G/T | 5.34316e-05 | 0.00516846 | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061638 | ATCCCTGGTTTGTAG[C/G/T]TTGGCGGTGCTGGAG | 79734 |
rs756795934 | in-del | -/TT | 2.04868e-05 | 0.00320046 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062513 | CCTGCCCTTCCCCTC[-/TT]TTTTTTCTAGCTGTT | 79734 |
rs757008342 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057901 | CATCATGCGATCATA[C/G]CAGTTCCTGACACAG | 79734 |
rs757067692 | snp | C/T | 3.33673e-05 | 0.00408442 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059405 | CCACAGCACCCCAAA[C/T]GGGCTGAGCTCAGAG | 79734 |
rs757300552 | snp | C/T | 1.818e-05 | 0.00301491 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059476 | GTGTCCGGAGAAGTC[C/T]CCTGTCTCCCTCCAC | 79734 |
rs757415606 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055097 | AGGGAGCTAGCCCTC[A/G]CCCGCCCCTTCTCGA | 79734 |
rs757456316 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052948 | AGGGCTTGAACTCAG[A/G]TCCATCTGACCCCAG | 79734 |
rs757565419 | snp | A/G | 3.36644e-05 | 0.00410257 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056365 | TCGGCCCGCTGATCC[A/G]CATCATCAAAGACCG | 79734 |
rs757677254 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056127 | GTGGCAGCCCCTCAG[C/G]CCCTTCCACAGGAAG | 79734 |
rs757843606 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053968 | CCAGCTTGAATATGT[C/T]ACTTCTCCTCACTGC | 79734 |
rs757897190 | in-del | -/G | 0.00174825 | 0.0295139 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051981 | GGGCGGCGAGCGGGC[-/G]GTGGGTCCTCCGCTC | 79734 |
rs758030293 | snp | C/T | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062471 | TCACCCCCTCCTTAC[C/T]GGCCCCACCTCCGCC | 79734 |
rs758167587 | in-del | -/AGAG | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050262 | TCAAAAAAGAAAAAG[-/AGAG]AGAGAGAGAGAGAGA | 79734 |
rs758214126 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060310 | GCCCACCCACCCCCA[C/G]CACTGCCAGGGCTGA | 79734 |
rs758441765 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058864 | CCCACCTCTGCTTCC[A/G]GGAGTGAAGGGAATA | 79734 |
rs758448853 | snp | A/C | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056332 | CAGGGGTCCTGGAGG[A/C]AGCCGAGTTCTACAA | 79734 |
rs758472432 | snp | C/T | 1.66078e-05 | 0.00288161 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059304 | TCTCCCCATGCTCCG[C/T]CCCTCTAGCTGGTGA | 79734 |
rs758531565 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052294 | GGGGAAGGAGTCGAC[C/G]AGGCTACTTCTCCCG | 79734 |
rs758564455 | snp | C/G | 1.66333e-05 | 0.00288381 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059390 | GGTGTCCAAGGAGCT[C/G]CACAGCACCCCAAAC | 79734 |
rs758691104 | snp | A/T | 0.000262953 | 0.0114633 | synonymous-codon, utr-variant-3-prime, missense, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062543 | TTACAAGCCAGAGGC[A/T]CCCGGATGTGAGGCC | 79734 |
rs758700821 | snp | A/G | 3.33067e-05 | 0.00408072 | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061676 | TGGAGCGAGGAGGGT[A/G]CTCATCTCTTGATCC | 79734 |
rs758972373 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056602 | CCCCAGACTCGGAGA[C/T]GGACACTGGGGTTCA | 79734 |
rs759017155 | snp | A/G | 1.92221e-05 | 0.00310011 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057523 | GGGGCGTGCCACCAG[A/G]ACAACCCTGGGACCT | 79734 |
rs759192503 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063271 | ACTCAGGAACTGCCC[A/G]GGGAGAGTGGGTATG | 79734 |
rs759208138 | snp | A/G | 0.000137466 | 0.00828941 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052603 | GGCCTTTGGCAAGTC[A/G]CCTCACCTCTCAATG | 79734 |
rs759320705 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059255 | GAGGTCTGTCGTATC[C/G]TGCCCCACGGCCCCC | 79734 |
rs759349743 | in-del | -/C | 2.68611e-05 | 0.00366468 | intron-variant, frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061491 | TGGCTGCAGGCCCTG[-/C]CCCCCCTCCTCTCCT | 79734 |
rs759364720 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054613 | AGAAAGTGACCTAAC[C/G]CCTCTGTGTCTGCAT | 79734 |
rs759398056 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051550 | CCATACACAGTGATT[G/T]GGCCAGAGGGCATCT | 79734 |
rs759464013 | snp | A/G | 3.74357e-05 | 0.00432625 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053207 | GGACATGGCTGAGGA[A/G]GGTGAGTTGGTCCAG | 79734 |
rs759466750 | snp | A/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050518 | TCTCAGAGAGGAAGT[A/T]GCTCAGGACACACCT | 79734 |
rs759678488 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059939 | GGATGAGGAAGCCAC[C/T]GCTGTAAATCCTGCC | 79734 |
rs760219436 | snp | A/G | 1.69841e-05 | 0.00291407 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056415 | ACGGTCACCCAGGTC[A/G]GGAGCAGGGGCAGCA | 79734 |
rs760270622 | snp | A/G | 2.4231e-05 | 0.00348065 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062623 | TGTACCATGGGGTGG[A/G]CCCCGGGCCTGAGAA | 79734 |
rs760350877 | snp | C/T | 0.000102192 | 0.00714742 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061062 | CCACTTGCCTGGCGC[C/T]TCACCCGCATAACCA | 79734 |
rs760448451 | snp | A/C | 1.70519e-05 | 0.00291987 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057388 | CTCTATGTGACCCTT[A/C]TGCCCACAGGTCCCA | 79734 |
rs760525335 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053594 | CAGGCATGGGGAGAG[C/G]TCTGTCTCTCTTTCT | 79734 |
rs760624408 | snp | A/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061731 | TGATTATCTCCACCC[A/G]CCAAAGTTTCTCATC | 79734 |
rs760844012 | in-del | -/AGCCC | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058139 | CAGAGCCAGAAAGTG[-/AGCCC]AGGGTCAAAAGTGCC | 79734 |
rs760920801 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060066 | TGAGAGCACCCTGGC[A/G]GCATCCACTGTACCA | 79734 |
rs760964634 | snp | A/G | 1.65899e-05 | 0.00288005 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059363 | CGAGGACCAGGCAGA[A/G]TTCCTGTGTGTGGTG | 79734 |
rs761372052 | snp | A/C | 1.69035e-05 | 0.00290714 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056407 | AGGACTACACGGTCA[A/C]CCAGGTCGGGAGCAG | 79734 |
rs761559188 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054632 | CTGTGTCTGCATGCC[A/C]CCATCTGTGAAATGG | 79734 |
rs761720526 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053872 | GCAGAGCTGCAGCCA[C/G]GGGCAAGGACTACAG | 79734 |
rs761748047 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050263 | CAAAAAAGAAAAAGA[A/G]AGAGAGAGAGAGAGA | 79734 |
rs761880321 | in-del | -/CCCCCC | 4.02212e-05 | 0.0044843 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059487 | GTCTCCTGTCTCCCT[-/CCCCCC]CCACCCTCCCCGCCT | 79734 |
rs762091786 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058090 | TATCCCTAGTCATGC[A/C]GCTGACCTCCCACCT | 79734 |
rs762092179 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062953 | ACCTCACAGGGTTGT[C/T]GTGAGGGTGCACAGA | 79734 |
rs762190959 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057172 | CTCAATGGAAAGTCC[C/T]GTAATGCCTAGGATT | 79734 |
rs762198990 | snp | A/G | 1.65924e-05 | 0.00288027 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057442 | GCAGTGCCAGGAGGA[A/G]GAGCTCACGCAAATG | 79734 |
rs762500530 | snp | C/T | 1.89159e-05 | 0.00307532 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062519 | CTTCCCCTCTTTTTT[C/T]TCTAGCTGTTACAAG | 79734 |
rs762670625 | snp | C/G | 4.74215e-05 | 0.00486914 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053224 | GTGAGTTGGTCCAGG[C/G]GGCTGGCCTGGACCT | 79734 |
rs762911894 | snp | A/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061755 | TCTCATCCGACCTTG[A/G]CCTTGGGGGTGAGGC | 79734 |
rs763253243 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059768 | TGTGTGACTTAGGAC[A/G]GGGCTTGTCCTCTCC | 79734 |
rs763482029 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058238 | GGAGACTGCAAGGCA[A/G]AAGGTCGGAGCCCCC | 79734 |
rs763509021 | snp | C/G | 2.19368e-05 | 0.00331178 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061613 | CCCCTCGCCCGCCCC[C/G]AGAGCTGCCATCCCT | 79734 |
rs763640868 | in-del | -/T | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062513 | CCTGCCCTTCCCCTC[-/T]TTTTTTTCTAGCTGT | 79734 |
rs763707679 | snp | C/T | | | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060827 | CTGGTTCACAGAGCA[C/T]GGAGGAGCAGCTGGA | 79734 |
rs763728546 | in-del | -/CAC | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054667 | CCATAGCACCCACCT[-/CAC]CGAGCTGTCATGAGG | 79734 |
rs763745590 | snp | C/T | 1.85558e-05 | 0.00304591 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062522 | CCCCTCTTTTTTTTC[C/T]AGCTGTTACAAGCCA | 79734 |
rs763792311 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053719 | AGTGCTGGCTGTGGG[C/T]GGAGGCAGGAGAGGG | 79734 |
rs763833365 | in-del | GATAGG/TAGGGGTCTC | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050299 | AGAGAGAGAGAGAGA[GATAGG/TAGGGGTCTC]ACTATGCTGTCCAGG | 79734 |
rs763981778 | snp | A/G | 4.7399e-05 | 0.00486798 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053225 | TGAGTTGGTCCAGGG[A/G]GCTGGCCTGGACCTT | 79734 |
rs764183636 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060179 | GAGCAGGCGTGAACC[A/C]GGCTGGGAAGAAGGC | 79734 |
rs764361408 | snp | A/G | 1.71108e-05 | 0.00292491 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056427 | GTCGGGAGCAGGGGC[A/G]GCACACACGGCCAGG | 79734 |
rs764393541 | snp | C/T | | | intron-variant, synonymous-codon | KCTD17 | GRCh38.p7 | 22:37061747 | CCAAAGTTTCTCATC[C/T]GACCTTGGCCTTGGG | 79734 |
rs764412806 | snp | C/T | 2.67469e-05 | 0.00365688 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062632 | GGGTGGGCCCCGGGC[C/T]TGAGAAGGAAGAAGC | 79734 |
rs764454485 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37052418 | GTTGGCCCAGCGGGC[A/C]CTATTTCTGAGCACC | 79734 |
rs765037421 | snp | A/G | 0.00010659 | 0.00729958 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061608 | CTCGGCCCCTCGCCC[A/G]CCCCCAGAGCTGCCA | 79734 |
rs765044487 | in-del | -/T | | | intron-variant, frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061498 | AGGCCCTGCCCCCCC[-/T]CCTCTCCTCCCGGCC | 79734 |
rs765318003 | snp | A/G | 5.19701e-05 | 0.00509729 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059451 | AAGGTGAGCCCACCC[A/G]CCTCAGCCTGTGTCC | 79734 |
rs765351259 | snp | A/G | 1.66161e-05 | 0.00288232 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059385 | TGTGTGGTGTCCAAG[A/G]AGCTCCACAGCACCC | 79734 |
rs765502882 | snp | A/G | 1.75931e-05 | 0.00296584 | missense, utr-variant-3-prime, synonymous-codon, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062539 | GCTGTTACAAGCCAG[A/G]GGCACCCGGATGTGA | 79734 |
rs765511833 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063098 | GAGATTCAGGTATTG[A/G]GGATGCAGGTTGTGG | 79734 |
rs765566941 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050265 | AAAAAGAAAAAGAGA[A/G]AGAGAGAGAGAGAGA | 79734 |
rs765705394 | snp | C/T | 2.54638e-05 | 0.00356809 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062627 | CCATGGGGTGGGCCC[C/T]GGGCCTGAGAAGGAA | 79734 |
rs766154618 | snp | C/T | 2.27002e-05 | 0.00336891 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061518 | TCCTCCCGGCCTCCT[C/T]CTCACGTTTCCTCCT | 79734 |
rs766169290 | snp | G/T | 0.000696621 | 0.0186501 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051754 | GATGCAGACGCCGCG[G/T]CCGGCGATGAGGATG | 79734 |
rs766251975 | snp | A/G | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061785 | CTCTGAGAGGAGAAG[A/G]AAGTTAGGGAGTGGG | 79734 |
rs766347046 | in-del | -/AGC | 0.000168535 | 0.00917817 | cds-indel, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060845 | AGGAGCAGCTGGAGG[-/AGC]AGCAGCAGCAGGAGG | 79734 |
rs766521424 | snp | C/G | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062462 | TGCCCTGCATCACCC[C/G]CTCCTTACCGGCCCC | 79734 |
rs766533627 | snp | A/C | 1.66181e-05 | 0.00288249 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059294 | CCTGCATTTTTCTCC[A/C]CATGCTCCGCCCCTC | 79734 |
rs766764630 | snp | A/G | 1.65932e-05 | 0.00288034 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059371 | AGGCAGAGTTCCTGT[A/G]TGTGGTGTCCAAGGA | 79734 |
rs766817883 | in-del | -/AC | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057911 | TCATAGCAGTTCCTG[-/AC]ACAGTTTTCAGGGTC | 79734 |
rs766909394 | snp | A/G | 1.82807e-05 | 0.00302325 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056315 | ATCTGTTCTGTCTGT[A/G]CCAGGGGTCCTGGAG | 79734 |
rs767089044 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055732 | AGTTGGGGGAATGCA[G/T]GGACACAAGGGTATG | 79734 |
rs767117645 | in-del | -/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057506 | CAGGTGCGCTGGGGA[-/C]AGGGGCGTGCCACCA | 79734 |
rs767303668 | snp | C/T | 0.000101128 | 0.0071101 | intron-variant | KCTD17 | GRCh38.p7 | 22:37061054 | TAGCTCAGCCACTTG[C/T]CTGGCGCCTCACCCG | 79734 |
rs767342119 | snp | A/G | 1.65603e-05 | 0.00287747 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059480 | CCGGAGAAGTCTCCT[A/G]TCTCCCTCCACCCTC | 79734 |
rs767407010 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050524 | AGAGGAAGTTGCTCA[A/G]GACACACCTAGTGAA | 79734 |
rs767493300 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37063323 | CTGTGTTTGACTTCC[C/T]GGGATGGGTCCTTGC | 79734 |
rs767686948 | snp | C/T | 3.20077e-05 | 0.00400035 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051991 | CGGGCGGTGGGTCCT[C/T]CGCTCGCCCGACGCG | 79734 |
rs768163451 | snp | C/T | 5.09074e-05 | 0.00504491 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059421 | GGGCTGAGCTCAGAG[C/T]CCAGCCGCAAAACCA | 79734 |
rs768369293 | snp | C/G/T | 4.08766e-05 | 0.00452072 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062599 | TTCCCATCTGAAATC[C/G/T]TTTATTTTTGTACCA | 79734 |
rs768449989 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058049 | ATGCAGTTTACCCAT[C/T]GGGAGATCCTTATCC | 79734 |
rs768548820 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054504 | GGGGCTAGGGGATCA[C/T]GCAGGGCTATCCGGG | 79734 |
rs768618595 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062882 | TGCTCCTTCCTGGCC[C/T]GGTCACATTGCCTCC | 79734 |
rs768618810 | in-del | -/CC | 3.81174e-05 | 0.00436546 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059483 | AGAAGTCTCCTGTCT[-/CC]CCCTCCACCCTCCCC | 79734 |
rs768710127 | snp | C/G | 2.12438e-05 | 0.00325906 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057353 | CCCCTCCTGGGGTGC[C/G]TGGTGCTCCCACAGG | 79734 |
rs768777689 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055081 | CACATGGCAGAAAGA[C/G]AGGGAGCTAGCCCTC | 79734 |
rs768825730 | snp | C/T | 0.000133129 | 0.00815763 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060974 | AGCCGGAGCCTCCCG[C/T]CCACTCCTTGCTGGA | 79734 |
rs769225421 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051108 | TCACTCACCAGCAAT[A/G]TGAGTAGGGCGGTCA | 79734 |
rs769327426 | snp | C/T | 3.31741e-05 | 0.00407259 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059342 | CTCCTCCTACAACTA[C/T]GGCAGCGAGGACCAG | 79734 |
rs769516662 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060246 | AGGCTTACCTCTGGC[C/T]TCCTGTCTATCTGTC | 79734 |
rs769546982 | snp | C/G | 2.03971e-05 | 0.00319345 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062510 | CCTCCTGCCCTTCCC[C/G]TCTTTTTTTTCTAGC | 79734 |
rs769868923 | snp | A/G | 8.39609e-05 | 0.00647869 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056380 | GCATCATCAAAGACC[A/G]GATGGAAGAGAAGGA | 79734 |
rs769986062 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051158 | TCTGTAAAATGGGTA[G/T]AGCCCAAAATACCAG | 79734 |
rs770223692 | snp | A/G | 6.43066e-05 | 0.00567002 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060963 | TTGCTAAGCAAAGCC[A/G]GAGCCTCCCGCCCAC | 79734 |
rs770258767 | in-del | -/C | 9.32444e-05 | 0.00682741 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057516 | GGGGACAGGGGCGTG[-/C]CACCAGGACAACCCT | 79734 |
rs770268401 | snp | C/T | 0.000165166 | 0.00908603 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051907 | CGAGCAGAAGTCCTT[C/T]CTCAGCCGCCTGTGC | 79734 |
rs770513964 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055675 | CATATCCCTGGACTT[C/G]TGATGAGCTCGTGCA | 79734 |
rs770530808 | snp | A/G | 1.69928e-05 | 0.00291481 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057390 | CTATGTGACCCTTCT[A/G]CCCACAGGTCCCACC | 79734 |
rs770763960 | snp | A/G | 1.83869e-05 | 0.00303202 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057511 | GCGCTGGGGACAGGG[A/G]CGTGCCACCAGGACA | 79734 |
rs770794932 | snp | A/C/G | 0.000276593 | 0.0117571 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061596 | TGAGGGCTTCTCCTC[A/C/G]GCCCCTCGCCCGCCC | 79734 |
rs770795612 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056534 | TTGTCATGGGGAGGC[C/T]GAGCTGGCCTGTAAG | 79734 |
rs770889622 | snp | A/G | 6.91874e-05 | 0.00588123 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053196 | GTGCTGGACAAGGAC[A/G]TGGCTGAGGAGGGTG | 79734 |
rs771027813 | snp | A/G | 2.80422e-05 | 0.00374437 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062484 | ACCGGCCCCACCTCC[A/G]CCCCTCCCATCCTCC | 79734 |
rs771069982 | snp | A/G | 7.42639e-05 | 0.00609314 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053083 | CTTCTCTCACCGAGC[A/G]TCCCTCACCTCCATA | 79734 |
rs771250737 | snp | A/C | 1.68707e-05 | 0.00290432 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059429 | CTCAGAGTCCAGCCG[A/C]AAAACCAAGGTGAGC | 79734 |
rs771681455 | snp | C/T | 1.64958e-05 | 0.00287187 | utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062613 | CCTTTATTTTTGTAC[C/T]ATGGGGTGGGCCCCG | 79734 |
rs771757247 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058014 | GTCTTTATGGTGAAC[A/G]GTGGTTCCTCCCAGT | 79734 |
rs771766127 | snp | C/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050326 | TATGCTGTCCAGGCT[C/G]GTCTTGAACTTCTAT | 79734 |
rs771791144 | snp | C/T | 2.01323e-05 | 0.00317265 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057359 | CTGGGGTGCCTGGTG[C/T]TCCCACAGGTGCCCT | 79734 |
rs772026115 | snp | G/T | 1.85256e-05 | 0.00304342 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061580 | GAGGCTGAGCTTGCA[G/T]TGAGGGCTTCTCCTC | 79734 |
rs772217989 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055363 | AATTAGCCTTTCTTA[C/T]AAGAAGACTGATCCT | 79734 |
rs772222812 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061426 | GGAGGGGCGCAGCTG[C/T]ACCTCCTCTGTGCCC | 79734 |
rs772227012 | snp | C/T | 5.05038e-05 | 0.00502487 | intron-variant, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061500 | GCCCTGCCCCCCCTC[C/T]TCTCCTCCCGGCCTC | 79734 |
rs772567213 | snp | A/G | 6.44268e-05 | 0.00567532 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053180 | CCGGCATGGCAAGCT[A/G]GTGCTGGACAAGGAC | 79734 |
rs772668433 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053983 | CACTTCTCCTCACTG[C/T]GTCTCCACTGGTATC | 79734 |
rs772827668 | snp | C/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050499 | TGGCAAGAGAGAAAG[C/G]CAATCTCAGAGAGGA | 79734 |
rs772927623 | snp | C/T | 2.24495e-05 | 0.00335026 | utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062615 | TTTATTTTTGTACCA[C/T]GGGGTGGGCCCCGGG | 79734 |
rs772978903 | snp | C/T | 1.64852e-05 | 0.00287094 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061505 | GCCCCCCCTCCTCTC[C/T]TCCCGGCCTCCTCCT | 79734 |
rs773015272 | snp | C/T | 1.69738e-05 | 0.00291317 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056414 | CACGGTCACCCAGGT[C/T]GGGAGCAGGGGCAGC | 79734 |
rs773207977 | snp | G/T | 0.000141313 | 0.00840455 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052495 | CCTTCCCTGCACTGC[G/T]CTCAGCCTCCTTCCT | 79734 |
rs773393998 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053337 | TGCCTCTTCCCAGTC[A/G]GACGGGGCTGATTCC | 79734 |
rs773405042 | snp | C/T | 5.89837e-05 | 0.00543032 | missense, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061592 | GCAGTGAGGGCTTCT[C/T]CTCGGCCCCTCGCCC | 79734 |
rs773726512 | snp | A/G | 1.65886e-05 | 0.00287993 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059358 | GGCAGCGAGGACCAG[A/G]CAGAGTTCCTGTGTG | 79734 |
rs773764553 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055676 | ATATCCCTGGACTTG[C/T]GATGAGCTCGTGCAG | 79734 |
rs773825935 | snp | G/T | 1.66996e-05 | 0.00288956 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053226 | GAGTTGGTCCAGGGG[G/T]CTGGCCTGGACCTTA | 79734 |
rs773825942 | in-del | -/GACTGCT | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055041 | TTCTTCCGGATTGCA[-/GACTGCT]GACTTCTCGTTGTGT | 79734 |
rs773851474 | snp | A/G | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37049972 | TAGAGATGGGGGCCA[A/G]GCGCAGTGGCTCGCA | 79734 |
rs773882736 | snp | C/T | 1.82981e-05 | 0.00302468 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062525 | CTCTTTTTTTTCTAG[C/T]TGTTACAAGCCAGAG | 79734 |
rs774005791 | snp | C/T | 2.10888e-05 | 0.00324715 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057354 | CCCTCCTGGGGTGCC[C/T]GGTGCTCCCACAGGT | 79734 |
rs774245782 | snp | A/G | 1.6898e-05 | 0.00290667 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056402 | AGAGAAGGACTACAC[A/G]GTCACCCAGGTCGGG | 79734 |
rs774284734 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056535 | TGTCATGGGGAGGCC[A/G]AGCTGGCCTGTAAGG | 79734 |
rs774551776 | in-del | -/TCCA | 3.77565e-05 | 0.00434475 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059487 | AGTCTCCTGTCTCCC[-/TCCA]CCCTCCCCGCCTGTC | 79734 |
rs774675445 | snp | A/G | 5.8045e-05 | 0.00538694 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051978 | GGTGGGCGGCGAGCG[A/G]GCGGTGGGTCCTCCG | 79734 |
rs774903810 | snp | G/T | 1.65861e-05 | 0.00287972 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059347 | CCTACAACTACGGCA[G/T]CGAGGACCAGGCAGA | 79734 |
rs774983583 | snp | C/T | 2.12678e-05 | 0.00326089 | synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061609 | TCGGCCCCTCGCCCG[C/T]CCCCAGAGCTGCCAT | 79734 |
rs775109083 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058046 | CAGATGCAGTTTACC[C/T]ATCGGGAGATCCTTA | 79734 |
rs775342498 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056669 | AGGCTCGCCCTCTCC[A/G]GACCTTGATTTTCTC | 79734 |
rs775369238 | snp | A/T | 1.67899e-05 | 0.00289736 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056382 | ATCATCAAAGACCGG[A/T]TGGAAGAGAAGGACT | 79734 |
rs775421289 | snp | C/T | 1.90181e-05 | 0.00308362 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062518 | CCTTCCCCTCTTTTT[C/T]TTCTAGCTGTTACAA | 79734 |
rs775581598 | in-del | -/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054540 | GGGGATACACAGGGC[-/T]AGGGCTCATCCAGGG | 79734 |
rs775595228 | in-del | -/A | 1.87394e-05 | 0.00306094 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057518 | GGACAGGGGCGTGCC[-/A]CCAGGACAACCCTGG | 79734 |
rs775672461 | snp | C/T | | | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061712 | CTTGAGCCGAGCTTT[C/T]GGCTGATTATCTCCA | 79734 |
rs775783050 | snp | A/G | 1.75391e-05 | 0.00296129 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059461 | CACCCGCCTCAGCCT[A/G]TGTCCGGAGAAGTCT | 79734 |
rs775911747 | snp | C/G | 2.2935e-05 | 0.00338629 | intron-variant | KCTD17 | GRCh38.p7 | 22:37051956 | TCGGACCGGGTGAGG[C/G]CCCCGGGGTGGGCGG | 79734 |
rs776133872 | in-del | -/CT | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062399 | GTGACTCAACTGCCT[-/CT]CTCTCTCTCTCCCTC | 79734 |
rs776201042 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059659 | TCCCCAGGGTGCAGC[C/T]GGCGTGGACTCAGAG | 79734 |
rs776357158 | snp | A/C | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054551 | GGGCTAGGGCTCATC[A/C]AGGGGATAGGGGATC | 79734 |
rs776379609 | snp | A/C/T | 0.0001473 | 0.00858092 | intron-variant | KCTD17 | GRCh38.p7 | 22:37053085 | TCTCTCACCGAGCAT[A/C/T]CCTCACCTCCATAGG | 79734 |
rs776437906 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051128 | TAGGGCGGTCACTTC[G/T]CTTCTGTGGCTTCAT | 79734 |
rs776500999 | snp | C/T | 2.70984e-05 | 0.00368083 | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062485 | CCGGCCCCACCTCCG[C/T]CCCTCCCATCCTCCT | 79734 |
rs776530111 | in-del | -/C | 2.68611e-05 | 0.00366468 | intron-variant, frameshift-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061490 | TGGCTGCAGGCCCTG[-/C]CCCCCCCTCCTCTCC | 79734 |
rs776692919 | snp | C/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37053732 | GGTGGAGGCAGGAGA[C/G]GGGGGAGTCTGCTTC | 79734 |
rs776811694 | snp | A/G | 3.6243e-05 | 0.00425678 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053204 | CAAGGACATGGCTGA[A/G]GAGGGTGAGTTGGTC | 79734 |
rs776887682 | snp | C/T | 1.65952e-05 | 0.00288051 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059372 | GGCAGAGTTCCTGTG[C/T]GTGGTGTCCAAGGAG | 79734 |
rs776925322 | snp | A/C | 0.00224301 | 0.0334137 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059447 | AACCAAGGTGAGCCC[A/C]CCCGCCTCAGCCTGT | 79734 |
rs776941970 | snp | G/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37051137 | CACTTCGCTTCTGTG[G/T]CTTCATCTGTAAAAT | 79734 |
rs777054755 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062904 | ATTGCCTCCTTGAGC[C/G]TTAGTCCAGGGGGTC | 79734 |
rs777171270 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057088 | TTTCTTGAATTACCC[A/G]TGTTCCGGTTCTGTC | 79734 |
rs777231939 | snp | A/G | | | intron-variant, synonymous-codon, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061366 | AGCGTCCTGCCTGCC[A/G]CCTCCTGCGCCCCTT | 79734 |
rs777258312 | snp | A/T | 0.000136045 | 0.00824646 | intron-variant | KCTD17 | GRCh38.p7 | 22:37052639 | GATCTCTCTGTAGAG[A/T]CGCATGGAAGCCCAC | 79734 |
rs777313125 | snp | C/T | 0.000176258 | 0.00938605 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37051874 | GGTGTTCCTGACCAC[C/T]CGGCAGACGCTGTGC | 79734 |
rs777391972 | snp | C/T | 1.98191e-05 | 0.00314788 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061533 | CCTCACGTTTCCTCC[C/T]TGCAGGTTCCCGTCC | 79734 |
rs777509126 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37056477 | GAGAGGCTGAGAGAC[A/G]GGGCGGGAAGCAGAG | 79734 |
rs777529946 | snp | A/C | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050783 | AGGAGACAGCTTCCT[A/C]GTCAGCCCTTGTCCC | 79734 |
rs777548911 | snp | A/G | | | intron-variant, utr-variant-3-prime | KCTD17 | GRCh38.p7 | 22:37062299 | CTGGATGGGTTAGTT[A/G]GGGAGCCCTTGCTGC | 79734 |
rs777747471 | snp | A/G | 1.82075e-05 | 0.00301719 | intron-variant | KCTD17 | GRCh38.p7 | 22:37057507 | AGGTGCGCTGGGGAC[A/G]GGGGCGTGCCACCAG | 79734 |
rs777914529 | in-del | -/A | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060579 | CTCGCTCTATGTAAC[-/A]GCAGCCAGGCTGACC | 79734 |
rs778013908 | snp | A/C | 1.75237e-05 | 0.00295999 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062544 | TACAAGCCAGAGGCA[A/C]CCGGATGTGAGGCCC | 79734 |
rs778151846 | in-del | -/AGAG | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050260 | TCTCAAAAAAGAAAA[-/AGAG]AGAGAGAGAGAGAGA | 79734 |
rs778304882 | snp | C/T | 3.3117e-05 | 0.00406908 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057419 | CCCAAGCACGTGTAC[C/T]GCGTGCTGCAGTGCC | 79734 |
rs778374017 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37054304 | CAGCTGCGTCGCAGC[C/T]AGCACCTGTTTACAC | 79734 |
rs778378883 | snp | C/T | 0.000122572 | 0.00782756 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061155 | TCCCACCACTGCCTC[C/T]TCCTCCGCTTCCCGC | 79734 |
rs778431697 | snp | A/G | 0.000159834 | 0.0089382 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37060832 | TCACAGAGCACGGAG[A/G]AGCAGCTGGAGGAGC | 79734 |
rs778542159 | snp | A/C | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050850 | CCCCCATCCTGAGGT[A/C]CACAGAATGACGGTT | 79734 |
rs778784047 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37057903 | TCATGCGATCATAGC[A/G]GTTCCTGACACAGTT | 79734 |
rs778840957 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055106 | GCCCTCGCCCGCCCC[G/T]TCTCGAGAGCTTGTT | 79734 |
rs778936966 | in-del | -/A | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37058172 | CCTTTAGAGAAGGAG[-/A]GGGGGTTGGCTAGCC | 79734 |
rs779033898 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059813 | CACTCTCTGAAGTGA[A/G]AGGGGAGGATCACAT | 79734 |
rs779239000 | snp | C/T | 1.83788e-05 | 0.00303135 | missense, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061554 | GTTCCCGTCCGCACC[C/T]TCTCAGACCTGAGGC | 79734 |
rs779419409 | snp | A/G | 1.64874e-05 | 0.00287113 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053172 | AACTTCCTCCGGCAT[A/G]GCAAGCTGGTGCTGG | 79734 |
rs779463077 | snp | A/G | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37059135 | GGCACAGGTTGCAAG[A/G]GGGAAGACTCCACCT | 79734 |
rs779473016 | snp | A/G | 0.000139253 | 0.00834309 | intron-variant, missense | KCTD17 | GRCh38.p7 | 22:37061667 | AGGGAGGGGTGGAGC[A/G]AGGAGGGTGCTCATC | 79734 |
rs779508572 | snp | C/T | 0.00142742 | 0.0266771 | intron-variant | KCTD17 | GRCh38.p7 | 22:37059483 | GAGAAGTCTCCTGTC[C/T]CCCTCCACCCTCCCC | 79734 |
rs779606178 | snp | A/G | 0.000116983 | 0.0076471 | synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37059411 | CACCCCAAACGGGCT[A/G]AGCTCAGAGTCCAGC | 79734 |
rs779870701 | snp | C/T | 1.82108e-05 | 0.00301746 | missense, utr-variant-3-prime, downstream-variant-500B, synonymous-codon, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062578 | ATCACCTCCAGGGAC[C/T]TGGGGTTCCCATCTG | 79734 |
rs780004551 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060523 | TCAGGGATACCCCAG[C/T]CCCACACCCTCCCTG | 79734 |
rs780203673 | snp | G/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37055390 | TCCTACCCTGGGGAC[G/T]CTACCCCCATGATCT | 79734 |
rs780378628 | snp | A/C | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050904 | AACTCAGAAAGCCAC[A/C]CGCAGAACCAATCCC | 79734 |
rs780553079 | snp | C/T | 1.88315e-05 | 0.00306845 | missense, synonymous-codon, intron-variant, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061544 | CTCCTTGCAGGTTCC[C/T]GTCCGCACCCTCTCA | 79734 |
rs780607745 | in-del | -/AGAGAG | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050260 | TCTCAAAAAAGAAAA[-/AGAGAG]AGAGAGAGAGAGAGA | 79734 |
rs780680667 | snp | A/G | | | downstream-variant-500B | KCTD17 | GRCh38.p7 | 22:37063768 | AAATATAAACACCCC[A/G]CCCTCTCCCTTCTCT | 79734 |
rs780719699 | snp | C/T | | | intron-variant | KCTD17 | GRCh38.p7 | 22:37060664 | AGCTGCCCAGGGGAC[C/T]GGAGAAGATGCCCCC | 79734 |
rs780776912 | snp | C/T | 3.49095e-05 | 0.00417774 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37053148 | CCCACCTACTTCGGG[C/T]CCATCCTGAACTTCC | 79734 |
rs781117547 | snp | A/C | 1.68091e-05 | 0.00289901 | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37056367 | GGCCCGCTGATCCGC[A/C]TCATCAAAGACCGGA | 79734 |
rs781410115 | snp | G/T | 1.74882e-05 | 0.00295699 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056447 | ACACGGCCAGGGCAG[G/T]GGCCAGTGGGGAGAG | 79734 |
rs781509283 | snp | A/C | 3.14302e-05 | 0.00396411 | intron-variant, synonymous-codon, missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37061192 | TCCTGCCTCATCTTC[A/C]TCCACCTCTTCTTCC | 79734 |
rs781727680 | snp | A/G | 0.000279955 | 0.0118279 | intron-variant | KCTD17 | GRCh38.p7 | 22:37060940 | GCAGCCAACCCCCAG[A/G]AGGATGATTGCTAAG | 79734 |
rs781762947 | in-del | -/GA | 1.77634e-05 | 0.00298017 | intron-variant | KCTD17 | GRCh38.p7 | 22:37056458 | GCAGGGGCCAGTGGG[-/GA]GAGAGAGGCTGAGAG | 79734 |
rs786205860 | snp | A/G | | | missense, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37057420 | CCAAGCACGTGTACC[A/G]CGTGCTGCAGTGCCA | 79734 |
rs796124025 | snp | C/T | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050900 | GAATAACTCAGAAAG[C/T]CACCCGCAGAACCAA | 79734 |
rs796655432 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | KCTD17 | GRCh38.p7 | 22:37062862 | CCCCTGCTGCATGGT[G/T]GATGTGCTCCTTCCT | 79734 |
rs797015884 | in-del | -/AGAGAGAGAG | | | upstream-variant-2KB | KCTD17 | GRCh38.p7 | 22:37050260 | TCTCAAAAAAGAAAA[-/AGAGAGAGAG]AGAGAGAGAGAGAGA | 79734 |