| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs555233882 | snp | C/T | 8.62865e-05 | 0.00656779 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433298 | ACAGTCTGCTTCCTT[C/T]GTAGAATAGGTATTT | 54793 |
| rs555393321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448830 | TGAGGCAGGAGAATT[A/G]CTTCAACCCGGGAGG | 54793 |
| rs555433069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448151 | GAAAAAGAAAAGAGA[A/G]AAGGAAAGGAAAGGA | 54793 |
| rs555442452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432311 | TACATTAGATAACAC[A/G]TCTATCAAACTTATT | 54793 |
| rs555454499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449533 | CTAACTTGAATTGTC[A/G]TCTACTTCCATATGA | 54793 |
| rs555490159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440398 | TGATGCCTTTTATGC[C/T]TTCTCTGGAGTGAAC | 54793 |
| rs555529365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456074 | ACAATTCCTGGCGAG[C/T]ATATAACACAGCACC | 54793 |
| rs555571803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441778 | GGGTGGATTGCTTGA[A/G]CTCAGGAGTTCGAGA | 54793 |
| rs555669640 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450834 | CCAAATTTGTTACAA[C/T]GAACCTATATTACTT | 54793 |
| rs555747955 | in-del | -/GAAAG | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442026 | TAAATAAAATAAAAA[-/GAAAG]GAAAAGAAAGTTTCA | 54793 |
| rs555790648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435290 | TAGTTATAATTCCTG[G/T]CTCAAAGGCTCTTTG | 54793 |
| rs555795166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452366 | ACTGCAATGACTTTG[A/G]AAAACAATCTGGCAT | 54793 |
| rs555858596 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452810 | CTTTAATAAAGCAGT[A/G]AAAATGAATAAATTA | 54793 |
| rs555894422 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434882 | ACATATATATAAATA[C/T]ACACATATATGTAGA | 54793 |
| rs555927256 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458319 | CACCTTTTTCTCCTC[C/T]CGCCCTTCCCCTCCC | 54793 |
| rs555970784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445685 | AATTATGGTGGATCA[C/G]TGGTGATATCACTAC | 54793 |
| rs556019478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434499 | ATTTCACTATTTAAA[A/G]ATTAGGTCCTTCAAA | 54793 |
| rs556172521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437832 | CAGCCTGGGTGACAG[A/G]GCGAGACCCTGTCTC | 54793 |
| rs556177577 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458776 | GCTGAAAGGGACCCA[A/C]GCACCAGTCAGCCCC | 54793 |
| rs556191833 | in-del | -/A | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457580 | ATAAGGCAAAATAAT[-/A]AAAAAGAGTACAGAG | 54793 |
| rs556596407 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454683 | AATTTAAACCAAAGA[G/T]TCCAGTGATTAGAAC | 54793 |
| rs556756394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460115 | AAATAAAAAATGAAA[C/T]CTGTGACGTGTGTTT | 54793 |
| rs556768541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454198 | GCCCCCAACATGTTT[C/T]TGACCTAATACCAAA | 54793 |
| rs556868057 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428219 | TGAAATGATTTAAAT[A/G]TAATTTAGGCACATA | 54793 |
| rs556882012 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455199 | CACTTCACTCCAGCC[C/T]GGGTGGAAGAGCAAA | 54793 |
| rs556983881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453355 | GTGCGAGACTCTGTC[A/T]CAAAAAAAAAAAGGT | 54793 |
| rs557143302 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431212 | AGATGGGGGGAAGAC[-/T]TTTTTTTTAATCTGA | 54793 |
| rs557202923 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445801 | TAACAAGCAGGCGCA[G/T]ATAAAAGTGAAGAGA | 54793 |
| rs557246881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456929 | CTTTCTTAGAGTAAC[A/G]ACATACGTTTTAGAT | 54793 |
| rs557310196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450372 | CATAGGTTCAAATGG[C/T]ACATTACCTGGCTTA | 54793 |
| rs557420348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451059 | GAAAATTTCCCTTAA[A/G]TTGGGCCAATATACT | 54793 |
| rs557527768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438745 | TTGTGATGTAGATAG[A/G]GTCAAGAGTGCTTTT | 54793 |
| rs557569304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431281 | CATTCCCTAGCCCTA[C/G]TATTTTTATAGCAAG | 54793 |
| rs557628840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432069 | CTATCAAGTCTGCTA[A/G]CTAAACTGGCAAATT | 54793 |
| rs557790860 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447298 | AGGCTGAAGCATGAG[A/T]ATTGCTTGAACCCAG | 54793 |
| rs557858239 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439533 | TTAGTAAGTACAGAA[C/G]GTCAGGAGTTATAAA | 54793 |
| rs557914747 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455154 | CGCTTGAACCTGGGG[A/G]GCAGAGGTTGCAGTG | 54793 |
| rs557976463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448772 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGTGT | 54793 |
| rs558117778 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431104 | CCAAAATGCTGGGGT[C/T]ACAGGCATGAGCCAC | 54793 |
| rs558189929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441714 | AAAAATTAAAAAGAA[A/G]TGGTCAGACGTGGTG | 54793 |
| rs558256681 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434310 | TCGCCATGTTGGCTA[A/C]GATGGTCTTGACCTC | 54793 |
| rs558313972 | snp | A/G | 1.88163e-05 | 0.00306721 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458214 | CTTTCCGTTCTTGGG[A/G]CTGCCGTTCAGGAAC | 54793 |
| rs558447911 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433493 | TTTGTTCAAATTAGC[A/T]CAAACAGTAAAAGAA | 54793 |
| rs558516317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452128 | CCACTAGTAACTAAA[C/T]ACAGAACTCAATTTT | 54793 |
| rs558529002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444810 | CTACACATCCACCAT[A/T]CACCCAAATGTAAAT | 54793 |
| rs558941581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437777 | CACTTGAACCCAGGA[A/G]GCATAGGTTGCAGTG | 54793 |
| rs559126295 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439041 | GATGCGTATGGCTTA[A/C]ATATTTAGCTATATG | 54793 |
| rs559202554 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458866 | CGGACTGATTGGGTA[A/G]GAGCCAGCTCGTCGC | 54793 |
| rs559263896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459565 | CACAGAATTAGTACT[C/G]CTGTCAGGAGCTGCT | 54793 |
| rs559307987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440894 | CATGCTTTCAGCGCC[C/T]GTGAAAGAAAAAGCA | 54793 |
| rs559355965 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455553 | CATACTAGGAGAAGT[A/G]GCAGCTTCTGCCATT | 54793 |
| rs559441041 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434605 | TGAAAGTAACTAAAA[C/T]GCATATTTGGTAGAT | 54793 |
| rs559506194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454949 | CATTAAAATAAGCCG[A/G]GCATGGTGGCTCACG | 54793 |
| rs559655655 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451328 | TGCATTCTTCTTTAT[A/G]TAACTCTTTTGAGAA | 54793 |
| rs559764270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444966 | TATAACCTTCCATTG[C/T]AGACGTTTTTATTTC | 54793 |
| rs559774405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437406 | ACAAAAGACAGGCCG[C/G]GCTCACACCTGTAAT | 54793 |
| rs559837303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437975 | AATTACTTGGGGCAA[C/G]CTGTAGGCAATGTAA | 54793 |
| rs560125444 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459752 | TTTCTCCATTTCTTT[C/T]TGTTTAATTTGGCTT | 54793 |
| rs560166261 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452216 | AAGATGAGATAATTT[-/A]AAAAAAAAGATGAGA | 54793 |
| rs560484807 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456977 | TACAGAACAGGTTTA[C/G]AAAAAGTTAATAGTG | 54793 |
| rs560534881 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430176 | AGTTCAGGCTGATCA[C/T]CATAAATATGTATAA | 54793 |
| rs560597662 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453589 | ACCCGGGAGGCGGAG[A/G]TTGTATTGAGCCAGA | 54793 |
| rs560725192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439903 | TTAAATACTTGTCTG[C/T]CTATCCTGTAAGCAA | 54793 |
| rs560725258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430799 | CAGAATGGATTCCAA[A/C]ATAATAAATACACAC | 54793 |
| rs560786687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431478 | GACAATGGTTAGAGA[C/G]AAGGGTGACTAAACG | 54793 |
| rs561113591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442527 | CCAAAATTATATAAA[G/T]ATGGTGGATGGCAAT | 54793 |
| rs561125776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434841 | CTTCAAATAAACACA[A/G]ATAACTGTTATAAAT | 54793 |
| rs561183356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435941 | AGTACCTGCCACTGA[C/T]CAGCCCATATATTGC | 54793 |
| rs561206781 | in-del | -/TTT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451805 | CATGCATGTAAAATA[-/TTT]TTTTCTTTTATACCC | 54793 |
| rs561333824 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457888 | CGCCCGGGCGCCCAG[C/G]TGACCGCGGCCCTCC | 54793 |
| rs561396933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451419 | TTGTTTTTGTCCTCA[C/T]ACTGAGCCAAATAAA | 54793 |
| rs561602529 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458402 | ACCACACGCACGCAC[C/T]CTGTCCCACACCCAA | 54793 |
| rs561786122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448379 | AAGGTTACCAAGGCA[C/T]AGATGGGAATGGAGA | 54793 |
| rs562058294 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452488 | TCCTGTCACCTGCAG[C/G]ATCTGAACCACATTT | 54793 |
| rs562094997 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440305 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 54793 |
| rs562120846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450839 | TTTGTTACAATGAAC[C/G]TATATTACTTTTGTA | 54793 |
| rs562201022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444119 | TAAACTACGATCATA[G/T]AGTAAAAAATTTACT | 54793 |
| rs562261387 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444864 | GGACAATCAGTGCAC[A/T]TCCTCTTCCTCAACC | 54793 |
| rs562457059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436769 | AATACTAAAAGAGCT[C/T]TCATTTATCATTTAC | 54793 |
| rs562728827 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437328 | AGGGAATGCAGCCAG[A/G]ATACGTTTCCAATTC | 54793 |
| rs562740327 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458678 | CGGACGGCGGCTTCC[A/G]GCGTTACTGAGCAGG | 54793 |
| rs562755536 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456185 | AGGGAAACTTACTTG[-/A]AAAAAACAGAGATTA | 54793 |
| rs562921806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430099 | AACTCAGTTAATTTC[C/T]GGAAAACTGATGATA | 54793 |
| rs563046532 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453124 | TCCCAGTACTTTGGG[A/C]GGCTGAGGCGGGCAG | 54793 |
| rs563113268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453478 | GGCCAATATGGTGAA[A/T]CCCTGTCTCTACTAA | 54793 |
| rs563115075 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446065 | AATTACTGCTTAAGG[G/T]AAACAGCATAGCACC | 54793 |
| rs563126152 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446637 | AGTAGCACCTACTTC[A/G]GAAGGTATTATGAAA | 54793 |
| rs563214621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438879 | GGCATGATTTGCCCT[C/G]TTGACTACTCTAGTT | 54793 |
| rs563339784 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455018 | ATCACATGAGGTCAA[C/G]AGTTCAGGATCAGCC | 54793 |
| rs563449848 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442358 | AGACCAACACCTCAG[A/G]CCAGAATAAAATGCA | 54793 |
| rs563516122 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434462 | TTTTTTGTCCTTAAC[A/G]CAAACAAAGATGCCT | 54793 |
| rs563549275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441331 | TCCTGTCAGCCCTCT[C/T]TTCAAGTTAAGAAAA | 54793 |
| rs563560002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434709 | AATTCAATAAATGAC[C/T]ACCAAAAGCAAGATG | 54793 |
| rs563794350 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457159 | CGAATTTTCGGAGCA[C/T]GTTTACTCTACACTG | 54793 |
| rs563860430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430586 | AACTCAGGGCTCCCA[A/C]TGATTCTACATTATG | 54793 |
| rs563886717 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448319 | GATACCACTCACATG[A/C]AAGTACCCAACACAG | 54793 |
| rs563911393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437481 | GGAGTTCGAGACCAG[C/G]CTGGCCAACACATGG | 54793 |
| rs564180444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454448 | ACTCTGTGTTCAAGA[C/T]GTATAGAAACTCTGC | 54793 |
| rs564285367 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444112 | TCTATAATAAACTAC[A/G]ATCATATAGTAAAAA | 54793 |
| rs564540847 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429738 | ATAATCCTCTAAATG[-/T]TTTTTTTTTTAAATT | 54793 |
| rs564545243 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457047 | CATTCATGATAACTC[A/G]AGAACTCGAATTTAT | 54793 |
| rs564558512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447725 | CAAGAAAAATTTAAG[C/T]GGAACCAAGTGCATT | 54793 |
| rs564619719 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440064 | TAAAAAGCATGTTTT[G/T]TTTTTTTTTTTTGAG | 54793 |
| rs564697148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431675 | TAAATAATTGTGCTC[A/G]TGATAGGATTATACT | 54793 |
| rs564707711 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451951 | CACTAAATATTTTCT[A/G]ATCTGGCTGTCTGCC | 54793 |
| rs564719507 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447963 | AAACATGGTCTCTAC[-/A]AAAAAAATACAAAAA | 54793 |
| rs564799302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450736 | TGACCTCGTGATCCA[A/G]CCGCCTCAGCCTCCC | 54793 |
| rs564905508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449899 | AGGAACCCAAAGTAA[A/C]AAACTGATGAAATAC | 54793 |
| rs564916811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443196 | GAACCCAATAGCGAA[C/G]AGCCTCCCTAGCACC | 54793 |
| rs565124551 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435990 | TTTTAAAAAACTGCT[G/T]CAATTTCTATGCATT | 54793 |
| rs565138748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436629 | TGAACAGGTTTGCCA[C/G]AAGTATCTTTTACAT | 54793 |
| rs565201962 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427644 | TTCTCTATCCTAGTT[A/T]TCAGGCAAAAAATGT | 54793 |
| rs565346790 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458029 | CACGGGGGTCCTGAG[A/G]GTCGGGAGGAGGCCG | 54793 |
| rs565536779 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455854 | TGTGTCTTTCTAGAT[C/T]GGAAAAATCAAGTTT | 54793 |
| rs565549651 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439481 | TATGAGGAAAAAATT[A/G]CTAAATATAAGTTTT | 54793 |
| rs565612973 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440338 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 54793 |
| rs565722485 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445318 | CCTCATCTGTAAAAT[A/G]AAGGGTCTAGAACTG | 54793 |
| rs565744696 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448065 | CCTGCCAATTCAAGG[C/T]TGCAGTGAGCCAAGA | 54793 |
| rs565786632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432965 | AACAAATTAAGAAAC[A/G]ATACATTAAATCTAA | 54793 |
| rs565800867 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454005 | AACAACGTAATGGAT[A/T]CAAACCTGGATACTT | 54793 |
| rs565863416 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447200 | GGAGTTTGAGACCAG[A/C]CAGACCAACATGGAG | 54793 |
| rs565936791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455116 | TGTAATCCCAGCTAA[A/G]CAAGAGGCTGAGTTA | 54793 |
| rs566036468 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438306 | GGTCAAATAATATCT[-/T]TTTTTTTTTTTTTTG | 54793 |
| rs566065593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455883 | TTTCACATTATTTTA[C/T]ATTTTTAAGTGTAAG | 54793 |
| rs566306798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437630 | TTACAGTGAGCCGAG[A/G]TCGCGCCACTGCACT | 54793 |
| rs566328641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448712 | TTAAGCTCAGGAGTT[C/T]GAGACCAGCTTGGGC | 54793 |
| rs566331962 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441817 | GGCAACAGGGCAAAA[C/T]CCCAAAACCCCATCT | 54793 |
| rs566685570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452035 | ATACACAAGTATTTA[C/T]TGTGCATTATGTAAT | 54793 |
| rs566821195 | snp | A/G | 1.64909e-05 | 0.00287144 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446206 | GCCGAGTTTACTGCT[A/G]GCCACAGAAAGCAAA | 54793 |
| rs566853585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452721 | CACTGTCAATTTAAC[A/G]ACAAAATATAAAGAA | 54793 |
| rs566911849 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454600 | ATGGAAAAAGGATGA[C/T]AGGTACAAACAACAT | 54793 |
| rs566949344 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441926 | GGAGGATCACTTGAA[A/C]CCAGGAGGTTGAAGC | 54793 |
| rs567056690 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429640 | TCTAGTTTCCCTACA[C/T]CTATTAAATGAGTGC | 54793 |
| rs567056822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438398 | GTTTTGTATTTCACT[A/G]CAGAAACTGTAAGCC | 54793 |
| rs567342779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449252 | CCCAATTCAATGTTC[C/T]TGGCATAGTTGCCAT | 54793 |
| rs567560049 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447759 | AAAAATAATGTACAA[C/T]CCAAGTGTCCATAAG | 54793 |
| rs567757427 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450219 | GCTGTCTGCCTGGAT[C/T]CTAAAGGTCCAATAA | 54793 |
| rs567828452 | in-del | -/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457267 | GCAGCAGAGTATTTT[-/G]GCAACCAACACAGCG | 54793 |
| rs567846529 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457199 | AAAGCCATTTTTAAT[A/G]CCACTGGACAATTTC | 54793 |
| rs567859060 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450991 | CAAAGGGTGGTCAAT[G/T]AGAGAAAACAGAATT | 54793 |
| rs567986460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438505 | ATACCCAGGTTTTCT[C/T]TAAAAACCAAGGTTC | 54793 |
| rs567986580 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447094 | ACCTCTGAAAGTTAG[A/G]AATAAAAACTAGGTA | 54793 |
| rs568157028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440215 | AGGCGCCCGCCACTA[C/T]GCCCGGCTAATTTTT | 54793 |
| rs568172532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453892 | TCAAATATATTAAGA[A/T]ATGTTCAAGCTTAAA | 54793 |
| rs568193537 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459183 | AGTAAATTCGGTACC[A/G]AGGGGCGGGGTCGGG | 54793 |
| rs568242408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453265 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 54793 |
| rs568889703 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436131 | ATTAGATCTTGCATG[C/T]AAAAGAAAAACAAAG | 54793 |
| rs569081314 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430703 | CCCAAAACCAGCCCC[C/T]GACTCTGATCTGTGA | 54793 |
| rs569093395 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457369 | ATGTCTGCCTCGAAC[A/G]GTGAAAATTTCCCAA | 54793 |
| rs569104110 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432035 | CTATTGGATAGTGCT[A/G]ATATAGACCTATCAA | 54793 |
| rs569271404 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452490 | CTGTCACCTGCAGCA[C/T]CTGAACCACATTTCA | 54793 |
| rs569272803 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451060 | AAAATTTCCCTTAAG[G/T]TGGGCCAATATACTT | 54793 |
| rs569330592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437144 | TCCAAGGTACAGCAT[C/T]GGGCTACCACTCTGG | 54793 |
| rs569337925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444510 | TTGAACTTAACTGTC[C/T]TTGAATTTAAATTCA | 54793 |
| rs569339583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452631 | CTGATGCATGCTAAA[A/G]TTTGATTAACTACCT | 54793 |
| rs569392478 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428525 | GAATTCAGAACCCAT[C/T]TGGACACAGCTAATA | 54793 |
| rs569451508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445339 | TCTAGAACTGATTAA[A/C]TGCAAAGCAGTATAT | 54793 |
| rs569475971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437587 | GGAAGCTGAGGCAGG[A/C]GAATGGCGTGAATCC | 54793 |
| rs569487636 | snp | C/T | 0.00795532 | 0.062565 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429601 | CCAGGTAAACCCCCC[C/T]ACCCCATTCAAAAGG | 54793 |
| rs569803048 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433141 | TTTTCTGAGTCCTCA[A/C]TTTTGATTAGCATTT | 54793 |
| rs569847215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448571 | AAAAAAAATACTGCA[A/G]AGCACTTGGCACAGT | 54793 |
| rs569922766 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435102 | GTACAGTATATTGAG[A/G]AGATCAAGAACTAAT | 54793 |
| rs569978576 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450119 | AGTCTAGGTATAAAT[A/T]GAATTCAACTTTTAT | 54793 |
| rs570161337 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429467 | ATTCAATAAATATAA[C/T]TGCATATGTTGTGCT | 54793 |
| rs570277970 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445597 | CTCATGAAGATGAAG[-/T]TAAGGTGAACTACAC | 54793 |
| rs570297386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441715 | AAAATTAAAAAGAAA[C/T]GGTCAGACGTGGTGG | 54793 |
| rs570313279 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453234 | TGGTGGCACGTGCCT[C/G]TAATTCCAGCTACTC | 54793 |
| rs570316056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459270 | GCAGGCCAGGATCAG[C/T]GCAGGCTGTGAGTCC | 54793 |
| rs570382300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453228 | TGGGAGTGGTGGCAC[A/G]TGCCTGTAATTCCAG | 54793 |
| rs570485146 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438182 | ATATTTCTGACATTT[C/T]CTAGGCAAGTGGGAT | 54793 |
| rs570600663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441231 | AATAGACCAGAATAT[A/G]TCAGAAAATGAGTTC | 54793 |
| rs570622991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445510 | ATAACATAAGTGGCA[C/T]AGTCAATACTTAATT | 54793 |
| rs570805729 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446397 | TGCCCCCTTTTCTTC[C/T]ATGACTCATTTATTC | 54793 |
| rs570864378 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438465 | TAATGTTTTCAAAAC[A/C]AAAACATGTCACATA | 54793 |
| rs570945042 | snp | A/G | 3.50342e-05 | 0.0041852 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440723 | AAGATTGGGGATTCT[A/G]GGAAGATGGTAATGG | 54793 |
| rs571040713 | snp | C/T | 1.68119e-05 | 0.00289926 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446299 | TTTAATACATGTTAT[C/T]CCCCATAAGTTATAA | 54793 |
| rs571152636 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449363 | TGATATCCCCTCCTT[G/T]CCCTAACATCAACTT | 54793 |
| rs571293491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442661 | AAGGACTGGAGGTAA[A/G]TGTACGCTTGAAGAA | 54793 |
| rs571337886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434257 | GGCATGCACCACCAC[A/G]CCTGGCTAATTTTTG | 54793 |
| rs571424734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448164 | GAAAAGGAAAGGAAA[A/G]GAAAGAATAAAGAAA | 54793 |
| rs571547298 | snp | A/G | 4.94654e-05 | 0.00497295 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436358 | ATTAAGAAATTAGTG[A/G]AGTCTTTTGGGAGAT | 54793 |
| rs571551797 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452151 | TCAATTTTCTCTACC[C/T]ATACTTTTAGTCAAA | 54793 |
| rs571622318 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428079 | ATTAGATCTAAAATC[C/T]GCAGTTTCTAAGCAC | 54793 |
| rs571674157 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457331 | GCTGAGTTACTTCTA[C/G]GTATCATTTAGCAAC | 54793 |
| rs571774009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437996 | GGCAATGTAAAGAGT[C/T]TGGATGGAAACTGTA | 54793 |
| rs571851879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444417 | ATAGGAACTATTCCT[C/T]ACAATTATATAGACA | 54793 |
| rs571881844 | in-del | -/AAAA | 0.00358779 | 0.0422022 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453654 | GTGAGACTCCGACTC[-/AAAA]AAAAAAAAAAAAGGT | 54793 |
| rs571967004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453378 | AAAAAGGTGAGGGCC[A/G]GGCACGGTGGCTCAA | 54793 |
| rs571999012 | snp | A/G | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452940 | GGGAGACTGAGGAAG[A/G]AGGACTGCTTGAGGC | 54793 |
| rs572080661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446483 | CCAAAACAATCTACA[A/G]TCCTAAGGTGTGTTA | 54793 |
| rs572238155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454423 | TTGAATATTCTGAAG[C/T]AAAAAAAGCACTCTG | 54793 |
| rs572558316 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430986 | AGGCACTCACCACCA[C/T]GCCTGGCTAATTTTT | 54793 |
| rs572616227 | snp | A/G | 1.65149e-05 | 0.00287353 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440532 | CAAAGGGTACACAGT[A/G]CTTCTTTTGCATTCT | 54793 |
| rs572621759 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429616 | TACCCCATTCAAAAG[A/G]CAGCAATATCTAGTT | 54793 |
| rs572795036 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439256 | TAGTTACATAATTAT[A/G]TTGAAAGTCTAAATA | 54793 |
| rs572896876 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456971 | GCTAAGTACAGAACA[A/G]GTTTAGAAAAAGTTA | 54793 |
| rs572949699 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457420 | GGGTGGGGCAAAAGG[C/T]TGGGAAGGAAGAGAA | 54793 |
| rs573166082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427562 | TTTTACCTATGTGTA[C/G]AGACATGTTTCATCT | 54793 |
| rs573176961 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429051 | TAATAGTGTAAATAG[A/G]TAGAATTGCTTGATC | 54793 |
| rs573262765 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428750 | ATGCCTTTATTTTTA[C/T]GTCTATTTTTTTGGT | 54793 |
| rs573269392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444723 | GTTGTGTGCTTTGGA[A/G]ATGAAATAAACTGTC | 54793 |
| rs573285793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437213 | AGATTATGCCATTCC[A/G]TTCGGATATATATCC | 54793 |
| rs573494772 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25458510 | CTGACACTCTGCCGT[A/T]CCAACCAACCCGCGT | 54793 |
| rs573586841 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450062 | AGGCAATCAAAGTAC[-/A]ACAGGTATTTCCTTG | 54793 |
| rs573609240 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458835 | CGGCCCAGCTAGGAA[A/G]CGGCTGCGGTAGGGA | 54793 |
| rs573672770 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439753 | TCGATCCCAGCTGCT[C/G]TCTCAAAAAGATGCA | 54793 |
| rs573686830 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440430 | ATGTTTTTTTCTTCA[A/C]AAAAAGTTATAAAAA | 54793 |
| rs573832641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441199 | AAAAAGGACTGCAGA[A/T]GAAAGTTAAGAGGTT | 54793 |
| rs573907063 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448889 | CACCACACTCCAGCC[G/T]GGGCGACAAAGTGAG | 54793 |
| rs573925483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454936 | GATTGACTTTAAACA[C/T]TAAAATAAGCCGGGC | 54793 |
| rs573965301 | snp | A/G | 6.87203e-05 | 0.00586135 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435363 | TAAAATGATACTTAC[A/G]TCAAGCACTGATCCA | 54793 |
| rs574094956 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443139 | TTTATCTCTACCTAT[A/G]TATTTTCAATTCTGT | 54793 |
| rs574110823 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449676 | AAATTTTAATCTATT[A/T]AAATTAAAAGTTAAA | 54793 |
| rs574118925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452401 | TTGCAAAACTGAATA[C/T]TTACATATTCTAACA | 54793 |
| rs574583755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437913 | AGCTCTGCCACTCAC[C/T]ACTTTTTGGTGTTAG | 54793 |
| rs574694472 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444121 | AACTACGATCATATA[C/G]TAAAAAATTTACTTT | 54793 |
| rs574724436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430541 | TGTCTCCAACACCCC[C/T]AGATGGGACTGTCTA | 54793 |
| rs574896338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460120 | AAAAATGAAACCTGT[A/G]ACGTGTGTTTCTATG | 54793 |
| rs574922172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459708 | CATGGCTTATCCTTT[A/G]GGGTCTGCTTTGGTG | 54793 |
| rs575029250 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435812 | CTGCTAATAAGTATT[C/T]AAACCTAATTATATT | 54793 |
| rs575112642 | snp | A/C | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458876 | GGGTAAGAGCCAGCT[A/C]GTCGCTCTGTTAGGA | 54793 |
| rs575156791 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434432 | TCTCAAAGCGTTTTT[C/G]ACAAACATCTTTTTT | 54793 |
| rs575168680 | snp | A/C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447356 | TGCACCACTGCACTC[A/C/T]AGCCTTTATGACCAA | 54793 |
| rs575296448 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455527 | CTCTTTTTTTAGTCT[C/T]ATGGTTTATACATAC | 54793 |
| rs575306107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456424 | GCTCTTTTGTCAAAT[A/G]AGAATAATTATAAAT | 54793 |
| rs575340573 | snp | A/G | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427742 | AATTTAACACAAACA[A/G]ATTAAACGAATTATT | 54793 |
| rs575430582 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428323 | AATTCATTTCTGAAG[C/T]TGCTTTCCTTCACTT | 54793 |
| rs575557636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435748 | TAGCCCGGCTATAAT[A/T]CATTTCTGTGTAGAA | 54793 |
| rs575699943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430635 | TCATTATGTATTACA[A/G]TGTAATACTAGTAGA | 54793 |
| rs575718664 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443750 | GGACTGTATGGATCT[A/C]AATAAATCAAATACT | 54793 |
| rs575896102 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457683 | CCCCATTTTAAAAAT[C/T]CTGTCTGCGACCTCG | 54793 |
| rs575966891 | in-del | -/TGAA | 0.0097519 | 0.0691437 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454342 | TAAGTGTTCACTGAA[-/TGAA]TGAATGAATGAATGA | 54793 |
| rs576022888 | snp | C/G | 0.000988451 | 0.0222092 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439567 | AGCACAGATATAAAA[C/G]AGGTAAGATGAAATG | 54793 |
| rs576042580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454854 | TCAGTGACTCAGACT[A/G]TGAATTAGCCACTAA | 54793 |
| rs576138513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431303 | TATAGCAAGGAACTG[C/T]CCTTCTTTTTAAAGC | 54793 |
| rs576156108 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455161 | ACCTGGGGGGCAGAG[G/T]TTGCAGTGAGCTGAG | 54793 |
| rs576461340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431111 | GCTGGGGTTACAGGC[A/G]TGAGCCACTGCGCCT | 54793 |
| rs576481034 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439849 | CCCTTCTAATAGGGT[A/G]CTTCCTTTGATTTAA | 54793 |
| rs576555128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451286 | AGATGATTAAGTTAC[A/G]GAGAAAGTTGCAAAC | 54793 |
| rs576616431 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452174 | TAGTCAAATACATTT[G/T]AAATATTTACATGAT | 54793 |
| rs576626201 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433499 | CAAATTAGCTCAAAC[A/C]GTAAAAGAAAAAAAA | 54793 |
| rs576952226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444093 | ACGGCATGTAAAACA[C/T]GCATCTATAATAAAC | 54793 |
| rs577143807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437813 | AGATCACACCATTGC[A/G]CTCCAGCCTGGGTGA | 54793 |
| rs577464648 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458875 | TGGGTAAGAGCCAGC[C/T]CGTCGCTCTGTTAGG | 54793 |
| rs577543613 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441108 | AAACTCCCTTCCATG[C/G]ACAAAGCCCCATACT | 54793 |
| rs577639894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453431 | GAGGCTGAGGCTGGC[A/G]GATCACGAAGTCAGG | 54793 |
| rs577660904 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451126 | TCCAACTAATCATTC[A/G]CACATACTAACAATA | 54793 |
| rs577801950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453050 | AGATACCGTATGTCC[C/T]GAAGCTGATTTTTTA | 54793 |
| rs577952162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449756 | GGCTAATTGTTACCA[C/T]ATTGAATAGCACAAA | 54793 |
| rs577958516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442040 | AGAAAGGAAAAGAAA[A/G]TTTCAAACATAAAAG | 54793 |
| rs577973914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450326 | GCAGCACTAAAGAAG[C/T]ACATTCCTGAGCTGT | 54793 |
| rs578018712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442845 | TGAAAGTATTGAGTT[C/T]GTTACTCTGACATTT | 54793 |
| rs578021372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456179 | CTATGAGAGGGAAAC[C/T]TACTTGAAAAAACAG | 54793 |
| rs745463417 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448295 | GTCACAAAAGGATAA[A/C]TATTCTATGATACCA | 54793 |
| rs745467418 | snp | C/T | 8.92371e-05 | 0.00667912 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444373 | AGCTACCATCAAAAT[C/T]TAAAAATCACATTAA | 54793 |
| rs745567858 | snp | A/C | 1.67469e-05 | 0.00289364 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432668 | TCTGGGAGTAGTTTA[A/C]CTTAAAAATATAGTT | 54793 |
| rs745632181 | snp | C/T | 9.89022e-05 | 0.00703145 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436259 | CAGTTCTGACTTGGT[C/T]GGAGTTGCTAGCAAA | 54793 |
| rs745650344 | in-del | -/CACAAT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430840 | ACACACACACACACA[-/CACAAT]TTTTTTTTTGAAACG | 54793 |
| rs745696271 | in-del | -/C | 1.72636e-05 | 0.00293794 | splice-donor-variant | KCTD9 | GRCh38.p7 | 8:25435362 | CTAAAATGATACTTA[-/C]GTCAAGCACTGATCC | 54793 |
| rs745714585 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449024 | ATTGCATTATACACA[C/T]TCCTGGGACAAAGCG | 54793 |
| rs745722208 | snp | A/C | 3.29777e-05 | 0.00406051 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436362 | AGAAATTAGTGGAGT[A/C]TTTTGGGAGATAGCT | 54793 |
| rs745778368 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25436562 | AATTTACTAAAATAC[A/G]ATTAGTTCACATAAT | 54793 |
| rs745942106 | snp | C/T | 3.3065e-05 | 0.00406588 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429828 | AAAACATTTTCATCT[C/T]TTACATCTTCCTCCA | 54793 |
| rs746034705 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445751 | ATCTGGCCTTTGTAA[A/T]GATTATAAAATGCAA | 54793 |
| rs746304695 | snp | A/G | 3.29641e-05 | 0.00405968 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439555 | AGTTATAAAGTCAGC[A/G]CAGATATAAAACAGG | 54793 |
| rs746383475 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453976 | CAGATAAATTTTCAC[C/T]TTTCTCCAACTCTAA | 54793 |
| rs746420452 | snp | C/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439661 | TTTATTCACTAAAGT[C/G]CTCCTAAGAATTCAG | 54793 |
| rs746426103 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430675 | CACAATAAATGTAAC[A/G]CGCTTGAATCATCCC | 54793 |
| rs746487043 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449071 | CTAGGGCATTGCACA[C/T]GGCAAAGCTGGGGTT | 54793 |
| rs746537500 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428970 | TGAATATTAATGATG[C/T]ACCTTGGTTTTTTTG | 54793 |
| rs746579376 | snp | A/G | 2.34063e-05 | 0.00342091 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433460 | AAAGAGAAAAGTCCT[A/G]GTTGTAAGGTTCATA | 54793 |
| rs746667339 | snp | A/G | 1.65157e-05 | 0.0028736 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435429 | ATTTGCATGTGCAAG[A/G]TTACAGCGGCTTAAA | 54793 |
| rs746717644 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447435 | GCTAAACACGAAGCA[A/C]AGTCAGCTAGCTCAT | 54793 |
| rs746841527 | in-del | -/AACTT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439223 | AAAGTTAAAATCTTA[-/AACTT]ACAAAAATGTGAGTA | 54793 |
| rs746904525 | snp | C/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456994 | AAAAGTTAATAGTGA[C/T]GAGAAATGTAAACTT | 54793 |
| rs747059616 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430659 | TAGTAGAAATAAAGT[A/G]CACAATAAATGTAAC | 54793 |
| rs747155279 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431389 | CACCGCAATTTGAAG[C/T]TATTTCTTAATTTGT | 54793 |
| rs747229938 | in-del | -/ATTAC | 0.000179186 | 0.00946367 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436532 | TAATTTAGTGAATGT[-/ATTAC]ATTCATTTTGAATTT | 54793 |
| rs747230762 | snp | A/G | 1.64909e-05 | 0.00287144 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436374 | AGTCTTTTGGGAGAT[A/G]GCTACAATGAATGTA | 54793 |
| rs747282800 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438836 | CAAGTTGTAGAATCA[A/T]GACTCTAATTGAGAA | 54793 |
| rs747283137 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460371 | CACCCCTACAATATG[C/T]CGTCCGTTTCAGGAA | 54793 |
| rs747394113 | snp | C/T | 1.65012e-05 | 0.00287234 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429841 | CTTTTACATCTTCCT[C/T]CAGCCCCTAAAATTC | 54793 |
| rs747427900 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440617 | CAACATTTAATGTCA[A/G]CCAGTCTGTGTGGAA | 54793 |
| rs747552859 | snp | A/T | 1.65943e-05 | 0.00288043 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430012 | TGTAATTCATGTGGA[A/T]ATTTCAGGCCTTATC | 54793 |
| rs747558863 | in-del | -/AAG | 1.6752e-05 | 0.00289408 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446081 | AAACAGCATAGCACC[-/AAG]AAGTTGAGGCACACT | 54793 |
| rs747642198 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437187 | ACATTTCCCCTTCAA[C/G]AGGCATCCAAAGATT | 54793 |
| rs747656638 | in-del | -/AC | 1.64821e-05 | 0.00287067 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439563 | GTCAGCACAGATATA[-/AC]AAACAGGTAAGATGA | 54793 |
| rs747673386 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451391 | CATAAGCTCCAGTTA[A/G]TATATACTAAGATTG | 54793 |
| rs747681040 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450319 | CTGATAAGCAGCACT[A/G]AAGAAGTACATTCCT | 54793 |
| rs747711076 | in-del | -/GG | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444260 | TTTTTTTTTTTTTTT[-/GG]CAGATAAAATTGGCT | 54793 |
| rs747723543 | snp | C/G | 1.65228e-05 | 0.00287422 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436213 | CTGATAGAAATAATT[C/G]ATGTAAAAGCCTGCT | 54793 |
| rs747764000 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438931 | CCAGAACTTGGAGCC[A/C]AGTTACATTCTTAAT | 54793 |
| rs747906528 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458842 | GCTAGGAAACGGCTG[A/C]GGTAGGGACGGACTG | 54793 |
| rs748031321 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460026 | TTGATTTGATTATTA[C/G]GAATTGCATGCCTGT | 54793 |
| rs748055680 | snp | C/T | 3.30371e-05 | 0.00406417 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446239 | AGATAAAGTTCCATA[C/T]ACAGCAACCACCTGT | 54793 |
| rs748070830 | snp | A/G | 3.89894e-05 | 0.00441511 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458205 | CCCCGTTACCTTTCC[A/G]TTCTTGGGGCTGCCG | 54793 |
| rs748210551 | snp | C/G | 3.29451e-05 | 0.00405851 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460391 | CGTTTCAGGAAATGC[C/G]TCTTTCATTTTGGGA | 54793 |
| rs748260804 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453227 | CTGGGAGTGGTGGCA[C/T]GTGCCTGTAATTCCA | 54793 |
| rs748266204 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431605 | CACACTGAGTACACA[C/G]TACTAAAACCAAGGA | 54793 |
| rs748294065 | snp | A/T | 1.79078e-05 | 0.00299226 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439249 | ATGTGAGTAGTTACA[A/T]AATTATATTGAAAGT | 54793 |
| rs748393523 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458586 | CTGGCTAACCTAGCC[A/G]GGACGGAGGGAGGGA | 54793 |
| rs748436960 | snp | A/G | 1.78723e-05 | 0.00298929 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25444298 | GTCACTTACCAATAA[A/G]TGGCTCTCCTTCACA | 54793 |
| rs748448553 | snp | C/T | 4.94482e-05 | 0.00497209 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436316 | TGGTGAATGATCCTC[C/T]GGTGGTTGAGAATTC | 54793 |
| rs748489382 | snp | A/C | 1.65015e-05 | 0.00287237 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432462 | ATGAGATGCTTAGTA[A/C]GTCTAGAGTAATAAA | 54793 |
| rs748521483 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442851 | TATTGAGTTTGTTAC[G/T]CTGACATTTTTAGAT | 54793 |
| rs748565255 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444488 | TTCCAATGCTTTGTT[C/T]AACCCCTTGAACTTA | 54793 |
| rs748611697 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454370 | TGAATGATGAATTAA[C/T]CAGTATACAAAAGGC | 54793 |
| rs748642842 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438573 | ATCTGCTGAAGCTGA[C/G]AGGCATGTGACCTCA | 54793 |
| rs748675698 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449834 | AGAAAAAAAAAAATG[A/G]AGAAAAAAAAACACA | 54793 |
| rs748690727 | snp | A/G/T | 8.23616e-05 | 0.00641679 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460303 | ATGAATAATGCTGGT[A/G/T]TGTGATGATCTGCCT | 54793 |
| rs748831851 | in-del | -/ACACACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430809 | TCCAACATAATAAAT[-/ACACACAC]ACACACACACACACA | 54793 |
| rs749019124 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448259 | GAACCTTTTTGACAG[C/T]ATGCTAAATGAAATA | 54793 |
| rs749053503 | snp | A/G | 1.83538e-05 | 0.00302929 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458225 | TGGGGCTGCCGTTCA[A/G]GAACAGGGTCACCCG | 54793 |
| rs749081853 | in-del | -/C | 7.58409e-05 | 0.00615749 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444253 | CCATCTTTTTTTTTT[-/C]TTTTTTGGCAGATAA | 54793 |
| rs749140365 | snp | C/T | 0.000107745 | 0.007339 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458287 | TGAGCCGCCACCCTC[C/T]CACCTGGTCCTCCTC | 54793 |
| rs749164280 | snp | C/T | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435461 | TGGCCATTTTGAAGT[C/T]AATGTATCGAAGGTC | 54793 |
| rs749186770 | snp | A/G | 1.64882e-05 | 0.00287121 | stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436243 | TAATTACCTGGCATC[A/G]CAGTTCTGACTTGGT | 54793 |
| rs749212701 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448861 | CAGAGGTTGCAGTTA[C/G]CTGAGATCACACCAC | 54793 |
| rs749284056 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442202 | TATATTGAAAGGATC[C/T]ATCACATACTGAGAA | 54793 |
| rs749356147 | snp | A/C | 3.38989e-05 | 0.00411683 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439439 | ATAAAGAAAGTCCCC[A/C]ATAAACAAAAAATAA | 54793 |
| rs749385263 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434246 | CTTGAATTACAGGCA[C/T]GCACCACCACGCCTG | 54793 |
| rs749422962 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443029 | TAATATAAACTTTAA[A/G]TACTACTATGAAGCC | 54793 |
| rs749437883 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439610 | GTTACACTCACCTTT[G/T]TCCTTAAACATGTGG | 54793 |
| rs749476395 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455781 | TTTTCACATGTGAAG[G/T]CCGTCCCTTCTTACA | 54793 |
| rs749527711 | snp | A/G | 1.65589e-05 | 0.00287736 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429813 | AGAAAAGTGATAAGG[A/G]AAACATTTTCATCTT | 54793 |
| rs749661479 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445534 | CTTAATTTGTGTTCC[C/T]TTTACCATCTTCTTT | 54793 |
| rs749672612 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444619 | CTTTCTTATCAATTG[A/T]GAATGAATAATTATG | 54793 |
| rs749787273 | in-del | -/AA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433451 | CTGCAAAGAAAAGAG[-/AA]AAGTCCTGGTTGTAA | 54793 |
| rs749797054 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435848 | TATTTTATTAATTCA[A/G]TAATTCAAAACAGTT | 54793 |
| rs749843522 | snp | C/T | 1.71405e-05 | 0.00292745 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439276 | AAGTCTAAATAAACT[C/T]ACCCAATAAATTAAT | 54793 |
| rs749887714 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456294 | GGGAAATCAAATTCT[A/T]TTCTATTTGAGTAGC | 54793 |
| rs749920187 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444041 | ACTACCTTACTATGT[A/T]ACAGTTAATGAATAT | 54793 |
| rs749982736 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443987 | CATTCACCATCAAAG[-/A]AAAAATTTTCAAACA | 54793 |
| rs750112957 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428235 | TAATTTAGGCACATA[C/T]TGATTATGAAAATAG | 54793 |
| rs750114702 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445396 | ATTTATACAGAGACT[C/T]TGTATATCATTATAG | 54793 |
| rs750207659 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450035 | CATACTGCTTGGCAA[A/G]GACTATTTTCAAGGC | 54793 |
| rs750227473 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453133 | TTTGGGCGGCTGAGG[C/T]GGGCAGATCAGGAGG | 54793 |
| rs750237550 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430100 | ACTCAGTTAATTTCC[A/G]GAAAACTGATGATAC | 54793 |
| rs750382568 | snp | A/T | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460124 | ATGAAACCTGTGACG[A/T]GTGTTTCTATGCCAG | 54793 |
| rs750398534 | in-del | -/ACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430813 | ACATAATAAATACAC[-/ACAC]ACACACACACACACA | 54793 |
| rs750404072 | in-del | -/T | 0.118115 | 0.212383 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444244 | AATTGTCATTCCATC[-/T]TTTTTTTTTTTTTTT | 54793 |
| rs750423676 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428238 | TTTAGGCACATATTG[A/G]TTATGAAAATAGATT | 54793 |
| rs750451336 | snp | C/T | 8.23825e-05 | 0.00641751 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440577 | TACACACACACCTAC[C/T]GTGTAGTTGTAAAGT | 54793 |
| rs750479503 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438493 | ATAAAATTTTAGATA[C/T]CCAGGTTTTCTTTAA | 54793 |
| rs750511128 | snp | A/G | 1.64819e-05 | 0.00287066 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439564 | GTCAGCACAGATATA[A/G]AACAGGTAAGATGAA | 54793 |
| rs750587041 | snp | C/G | 0.000129761 | 0.00805379 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444260 | TTTTTTTTTTTTTTT[C/G]GCAGATAAAATTGGC | 54793 |
| rs750696814 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443919 | GTCAAACACTACTTA[C/T]GCAAGCAATATTTAC | 54793 |
| rs750701494 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446800 | TTAACGACATCAACT[A/G]CCACAGAAAAGATAA | 54793 |
| rs750757435 | in-del | -/TCTTT | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427768 | TTATTGGGGAGGCAG[-/TCTTT]TCTTTTGTTCAGAAT | 54793 |
| rs750818293 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446624 | AAATGAAGAAAATAG[C/T]AGCACCTACTTCAGA | 54793 |
| rs750827645 | in-del | -/AAAAAAAAAAAA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437848 | GCGAGACCCTGTCTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA | 54793 |
| rs751030985 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446410 | TCCATGACTCATTTA[C/T]TCACTTGGTGCCTAA | 54793 |
| rs751043534 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459435 | GGGCTCTGGGAGTAA[G/T]CCTGTCTGCCTGGCG | 54793 |
| rs751095753 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445443 | CTTCACATCACTGAT[A/T]AAAAAAACTCATGTT | 54793 |
| rs751168687 | snp | C/G/T | 6.67837e-05 | 0.00577824 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458193 | GCCCCCTCACGCCCC[C/G/T]GTTACCTTTCCGTTC | 54793 |
| rs751292843 | snp | A/G | 3.29451e-05 | 0.00405851 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460452 | GCCGAATTACCTCCT[A/G]ATCCTTGCACACCAG | 54793 |
| rs751321932 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437217 | TATGCCATTCCGTTC[A/G]GATATATATCCCTGG | 54793 |
| rs751540221 | snp | A/C | 1.65187e-05 | 0.00287386 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432582 | TAAGGTAGCCACTCT[A/C]AGGTTAATTCCTGTC | 54793 |
| rs751546034 | in-del | -/T | 1.64727e-05 | 0.00286986 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460398 | GAAATGCCTCTTTCA[-/T]TTTTGGGAACTGGGA | 54793 |
| rs751586766 | snp | A/G | 4.98542e-05 | 0.00499245 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446114 | GTTGACAGCTTATAA[A/G]AAGGTGAAGGTTACC | 54793 |
| rs751588193 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440499 | AGTATCTTTTAAGGA[A/T]ATCAGCAAATTGAAG | 54793 |
| rs751868125 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434164 | GAGTGCAGTGGTGCT[A/G]TCTCAGCTCACTGCA | 54793 |
| rs751882457 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443590 | GAGAAGTTCTTGCTT[A/T]CAGTTTTAAGGTAGA | 54793 |
| rs751884579 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448632 | ATTAAAGCCTGAGTA[A/G]GGCTGGGCGCGGTGG | 54793 |
| rs751912033 | snp | A/G | 1.65737e-05 | 0.00287864 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436443 | ACTTCTAGGTGTTCA[A/G]TCAATGAGTCAATAC | 54793 |
| rs751957788 | in-del | -/TAT | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427915 | AATTAAGTTATACTG[-/TAT]TATTTCCTTTGCTAC | 54793 |
| rs751965075 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432796 | TAAACAGTTTACTGA[C/T]GAAAGAATGCTTTCA | 54793 |
| rs752063135 | snp | A/T | 6.56505e-05 | 0.00572896 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444272 | TTTGGCAGATAAAAT[A/T]GGCTTTTAAAGTCAC | 54793 |
| rs752143797 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432064 | AACAGCTATCAAGTC[G/T]GCTAGCTAAACTGGC | 54793 |
| rs752160878 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435226 | AGACCTTTAGTCTTA[A/T]ATCAACATAATAAAT | 54793 |
| rs752217653 | snp | A/C | 1.64749e-05 | 0.00287005 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460232 | CATTGTTTTTCTTCA[A/C]CTCTTAGATGGATGC | 54793 |
| rs752303524 | snp | A/G | 8.24287e-05 | 0.00641931 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436334 | TGGTTGAGAATTCTT[A/G]AAAAAGACATTAAGA | 54793 |
| rs752384708 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455351 | CTTATTTCTAAATAT[A/C]TTGCTAACTAGGATG | 54793 |
| rs752535135 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441993 | TGAGTGATGAAGTGA[C/G]GCCCTGTCTCAAAAA | 54793 |
| rs752555205 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453759 | TACAGGAACGTGGAT[A/G]AACACATTATGTTAT | 54793 |
| rs752558280 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440891 | CAGCATGCTTTCAGC[A/G]CCTGTGAAAGAAAAA | 54793 |
| rs752665624 | snp | A/G | 4.94858e-05 | 0.00497398 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429950 | GTTGGCTTCTTGAAG[A/G]TCACACCCAGACAGA | 54793 |
| rs752679677 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449049 | AAAGCGAAGCGAAAT[A/C]CAGTACCTAGGGCAT | 54793 |
| rs752721190 | in-del | -/TA | 0.000131957 | 0.00812163 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432483 | AGTAATAAAAATTCT[-/TA]TAAAGTGTTGGTGAA | 54793 |
| rs752725577 | snp | A/C | 0.000169978 | 0.00921739 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435369 | GATACTTACGTCAAG[A/C]ACTGATCCAGAGAGA | 54793 |
| rs752762133 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448800 | TGTGCCTGTAGTCCC[A/C]GCTACTTGGGAGGCT | 54793 |
| rs752837527 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450562 | CAAGCCTGTAATGCC[A/G]GCACTTTTTGGGAGG | 54793 |
| rs752982088 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455727 | CTTCCATATCACAAT[A/G]TCAATGACAACCAAT | 54793 |
| rs753149503 | snp | A/C | 4.96142e-05 | 0.00498043 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458166 | CCCTCGCCCCGACCC[A/C]CGGCCCGCCGCGCCC | 54793 |
| rs753172549 | snp | C/T | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446142 | ACCTGATCAAAGCAA[C/T]ATCATCAATCAGTCC | 54793 |
| rs753209636 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456540 | TTCTTTTTATCTAGT[A/G]CTCTCCAGTTTGGAT | 54793 |
| rs753356297 | snp | A/G | 1.73564e-05 | 0.00294583 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436484 | TGCTTCTTCTAACAC[A/G]CCTATCAGAACAAAA | 54793 |
| rs753366998 | snp | A/G | 1.64879e-05 | 0.00287118 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436343 | ATTCTTAAAAAAGAC[A/G]TTAAGAAATTAGTGG | 54793 |
| rs753388873 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442456 | TATAATTAACACAGA[A/C]CAAGTTACACATACT | 54793 |
| rs753641098 | snp | C/T | 1.74921e-05 | 0.00295732 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440722 | TAAGATTGGGGATTC[C/T]GGGAAGATGGTAATG | 54793 |
| rs753661308 | snp | A/G | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427801 | ATTCATAAGGTTTGT[A/G]TTGTTAGCATGGTGT | 54793 |
| rs753675709 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443778 | ACTTTATCTTCCTTT[C/T]GGCCTTTTCTTTTGA | 54793 |
| rs753683687 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431638 | AAAATATAATCTTAG[A/G]TGAAAGTAATGTAAC | 54793 |
| rs753705593 | in-del | -/CAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430840 | ACACACACACACACA[-/CAC]AATTTTTTTTTTGAA | 54793 |
| rs753780195 | snp | A/C | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460257 | GGATGCCAATTCAAA[A/C]GACAAGCCCCCTGAA | 54793 |
| rs753809480 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453496 | CTGTCTCTACTAAAA[A/C]CACAAAAATAGCCAG | 54793 |
| rs753864866 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449885 | CTTTCCCATGACATA[A/G]GAACCCAAAGTAACA | 54793 |
| rs753938232 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450866 | TGTAATAAGGGGGGA[A/C]GTTTTAATTTATTTT | 54793 |
| rs754098205 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438383 | TAAAAGTTAATGGGT[A/G]TTTTGTATTTCACTA | 54793 |
| rs754261294 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456777 | TTGAGTGGATTTGGG[A/G]GAGATTTAGAGCAAA | 54793 |
| rs754296884 | snp | A/G | 1.66427e-05 | 0.00288462 | stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435392 | CAGAGAGATCAGCTC[A/G]TTCAAGATTTGCACA | 54793 |
| rs754318299 | snp | A/G | 1.79574e-05 | 0.00299639 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458264 | CGCTGCCCCCGCTGG[A/G]TCCTGAGTGAGCCGC | 54793 |
| rs754439120 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446454 | TCAACTAGAACATAA[C/G]AAATCATCTCTGACC | 54793 |
| rs754480824 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430987 | GGCACTCACCACCAC[A/G]CCTGGCTAATTTTTT | 54793 |
| rs754505710 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430390 | ATGGCTCAAGTTACA[A/G]CCTGAGCTCCACCTC | 54793 |
| rs754613129 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453377 | AAAAAAGGTGAGGGC[C/T]GGGCACGGTGGCTCA | 54793 |
| rs754623315 | snp | A/G | 1.79554e-05 | 0.00299623 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458273 | CGCTGGGTCCTGAGT[A/G]AGCCGCCACCCTCCC | 54793 |
| rs754635117 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434516 | TTAGGTCCTTCAAAC[-/G]TTTTTTTGATGTTAG | 54793 |
| rs754666366 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430185 | TGATCACCATAAATA[G/T]GTATAAACAAAGGTT | 54793 |
| rs754745319 | in-del | -/C | 3.30857e-05 | 0.00406716 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444254 | CATCTTTTTTTTTTT[-/C]TTTTTGGCAGATAAA | 54793 |
| rs754786774 | snp | A/G | 3.3413e-05 | 0.00408722 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439394 | TCTATGATCTTGCTT[A/G]TTTCCCCAGACACCT | 54793 |
| rs754790033 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431679 | TAATTGTGCTCGTGA[C/T]AGGATTATACTTAGG | 54793 |
| rs754802370 | snp | A/C | 1.64811e-05 | 0.00287059 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439573 | GATATAAAACAGGTA[A/C]GATGAAATGTGAAAA | 54793 |
| rs754872279 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438849 | CAAGACTCTAATTGA[C/G]AATTATGATTGCAAG | 54793 |
| rs755028293 | in-del | GAA/TGAGGGCCGGGCACGGT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453370 | TCAAAAAAAAAAAGG[GAA/TGAGGGCCGGGCACGGT]GGCTCAAGCCTGTAA | 54793 |
| rs755163885 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448640 | CTGAGTAGGGCTGGG[C/T]GCGGTGGCTCACGCC | 54793 |
| rs755206509 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460377 | TACAATATGTCGTCC[A/G]TTTCAGGAAATGCCT | 54793 |
| rs755294291 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460462 | CTCCTAATCCTTGCA[C/T]ACCAGATACTTTTAA | 54793 |
| rs755394013 | in-del | -/AGGG | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434749 | AAAAGACATACAGAC[-/AGGG]ACGGGCCTTGGTGGT | 54793 |
| rs755399607 | snp | G/T | | | upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25458508 | GACTGACACTCTGCC[G/T]TACCAACCAACCCGC | 54793 |
| rs755434895 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455399 | CTAATATTTCAAAGA[A/G]TAACATACACTTAGG | 54793 |
| rs755436158 | snp | C/T | 0.000230558 | 0.0107343 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444275 | GGCAGATAAAATTGG[C/T]TTTTAAAGTCACTTA | 54793 |
| rs755467588 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438347 | ATGTTCAAGGGAATA[C/T]AAAGTTTGTTATAGC | 54793 |
| rs755484751 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435880 | ATTAGGCAAAAATGA[G/T]TACTGTGGTCTTTAC | 54793 |
| rs755520623 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454319 | GCCACATACTCAGAA[A/G]GCATTTACTAAGTGT | 54793 |
| rs755525573 | snp | A/G | 1.66217e-05 | 0.0028828 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432643 | AGATTAGCACCTACA[A/G]TGAACACATTCTGGG | 54793 |
| rs755638608 | snp | C/T | 1.64732e-05 | 0.0028699 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460241 | TCTTCACCTCTTAGA[C/T]GGATGCCAATTCAAA | 54793 |
| rs755708012 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432124 | TTGAAAAAGATGACC[A/C]GGCAAAATTATAATC | 54793 |
| rs755816376 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452865 | GAAGAGAATTATATT[C/G]AACGAAAAAAGCAAG | 54793 |
| rs755855498 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431915 | ATTTAAAAATCAATT[-/T]CTCATTTGCACTAGC | 54793 |
| rs755922048 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442027 | AAATAAAATAAAAAG[A/G]AAGGAAAAGAAAGTT | 54793 |
| rs755931641 | snp | A/T | 1.65778e-05 | 0.002879 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429808 | GAGAAAGAAAAGTGA[A/T]AAGGAAAACATTTTC | 54793 |
| rs755940017 | snp | C/T | 1.64961e-05 | 0.00287189 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429951 | TTGGCTTCTTGAAGA[C/T]CACACCCAGACAGAT | 54793 |
| rs755957874 | in-del | -/A | 1.67939e-05 | 0.0028977 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435519 | TTCAAACCCTGAAAT[-/A]AAAAAAGCACAAATT | 54793 |
| rs756048526 | snp | C/G/T | 5.38695e-05 | 0.00518964 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458278 | GGTCCTGAGTGAGCC[C/G/T]CCACCCTCCCACCTG | 54793 |
| rs756360385 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434209 | AGTTCAAGTGATTCT[C/T]GTGCCTCAGCCTCCT | 54793 |
| rs756362834 | snp | A/G | 1.69129e-05 | 0.00290795 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439421 | ACCTGTGTCACCATT[A/G]TAATAAAGAAAGTCC | 54793 |
| rs756452997 | snp | A/G | 3.29538e-05 | 0.00405904 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439593 | AAATGTGAAAACAAC[A/G]TGTTACACTCACCTT | 54793 |
| rs756693128 | snp | C/T | 1.68604e-05 | 0.00290343 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435376 | ACGTCAAGCACTGAT[C/T]CAGAGAGATCAGCTC | 54793 |
| rs756749914 | snp | A/G | 1.76808e-05 | 0.00297323 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436493 | TAACACACCTATCAG[A/G]ACAAAAATAATTCTG | 54793 |
| rs756836046 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443811 | TATACAACTATAAGC[C/T]TTCTTCCAAATCAAA | 54793 |
| rs756953006 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442460 | ATTAACACAGAACAA[A/G]TTACACATACTAAAG | 54793 |
| rs757136542 | snp | A/G | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460259 | ATGCCAATTCAAAAG[A/G]CAAGCCCCCTGAAAC | 54793 |
| rs757224022 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427853 | ATAATCATGTTTAAA[G/T]AAATAAATTTACTTT | 54793 |
| rs757224499 | snp | A/C | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460356 | ACAGAGAGTTGTCCT[A/C]ACCCCTACAATATGT | 54793 |
| rs757248786 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432571 | TTGCATTTTTTAAGG[-/T]TAGCCACTCTCAGGT | 54793 |
| rs757427010 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441634 | AAGCAAAAGAAATAC[-/A]AGAGTGATTAAACAC | 54793 |
| rs757514617 | snp | A/G | 8.28205e-05 | 0.00643455 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429816 | AAAGTGATAAGGAAA[A/G]CATTTTCATCTTTTA | 54793 |
| rs757552362 | snp | C/T | 1.65573e-05 | 0.00287721 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435406 | CGTTCAAGATTTGCA[C/T]AGCAAAGATTTGCAT | 54793 |
| rs757603030 | snp | A/G | 1.65239e-05 | 0.00287431 | intron-variant | KCTD9 | GRCh38.p7 | 8:25429976 | ACAGATCACAATTCT[A/G]CAAGATGAAAACAAT | 54793 |
| rs757720494 | snp | C/G | 4.96405e-05 | 0.00498175 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436192 | AAAATTTTATTCATA[C/G]ATTTGCTGATAGAAA | 54793 |
| rs757731920 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458465 | TAGGCTCCTCAGCCT[A/G]CCTGGGGCCCTTCCC | 54793 |
| rs757814684 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430484 | GTGAGGGATCTAGGT[A/G]GGGTACTCCTCATGA | 54793 |
| rs757950132 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444080 | CCAGAGCATTTTAAC[A/G]GCATGTAAAACATGC | 54793 |
| rs757991026 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430153 | TTCTATCTTTATTTG[C/T]TACCTCTAGTTCAGG | 54793 |
| rs758074131 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25436768 | AAATACTAAAAGAGC[-/T]TTCATTTATCATTTA | 54793 |
| rs758074672 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428598 | TAGGGAGGTACAGGC[C/T]CTTCCTCTGCTGCTG | 54793 |
| rs758077181 | snp | C/T | 1.64901e-05 | 0.00287137 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446201 | TTTATGCCGAGTTTA[C/T]TGCTGGCCACAGAAA | 54793 |
| rs758154920 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435151 | ATTAGTTACTAAACC[G/T]TTCAAGTCTATGTTT | 54793 |
| rs758162834 | snp | C/T | 5.34674e-05 | 0.00517019 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458187 | CGCCGCGCCCCCTCA[C/T]GCCCCCGTTACCTTT | 54793 |
| rs758286560 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438549 | CTGACCACTTTGCAC[A/G]TGGCAATGATCTGCT | 54793 |
| rs758295240 | snp | A/G | 1.92284e-05 | 0.00310061 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436524 | AAACAACCTAATTTA[A/G]TGAATGTATTACATT | 54793 |
| rs758308116 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450038 | ACTGCTTGGCAAGGA[C/G]TATTTTCAAGGCAAT | 54793 |
| rs758382014 | snp | A/G | 1.66532e-05 | 0.00288554 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439361 | GTACTCAGGACTTCG[A/G]TCAATTAAGAAAGCT | 54793 |
| rs758390925 | snp | A/G | 2.5345e-05 | 0.00355976 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444264 | TTTTTTTTTTTGGCA[A/G]ATAAAATTGGCTTTT | 54793 |
| rs758429559 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451103 | AGGGCTATTCTTGAC[C/G]TTTGTTTTCCAACTA | 54793 |
| rs758480792 | snp | G/T | 0.00818209 | 0.0634358 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432571 | TTTGCATTTTTTAAG[G/T]TAGCCACTCTCAGGT | 54793 |
| rs758493805 | snp | C/T | 1.65663e-05 | 0.002878 | intron-variant | KCTD9 | GRCh38.p7 | 8:25429997 | TGAAAACAATATTCA[C/T]GTAATTCATGTGGAA | 54793 |
| rs758845909 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447825 | ACAATGGAATATTAT[C/T]CAGCAATAAGAAACA | 54793 |
| rs758881711 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441358 | AAAAACTAATTTCAT[A/G]TAAAAATGAGCAATA | 54793 |
| rs758882223 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431313 | AACTGCCCTTCTTTT[C/T]AAAGCCCCAAAGGTA | 54793 |
| rs758971175 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440418 | CTGGAGTGAACCATG[-/T]TTTTTTCTTCAAAAA | 54793 |
| rs759001688 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432436 | TTTGTTTTGATTTCA[A/G]TAAATTTTGCATGAG | 54793 |
| rs759064331 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431966 | GCTATATATGGGTGG[C/T]AGCTACTATACTGAA | 54793 |
| rs759143267 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456817 | GACTAGGTTTAAATA[-/TT]TGTCTTCCATGAGTA | 54793 |
| rs759177645 | snp | A/T | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459527 | GGGGCATTTCTAGGC[A/T]CTTTGTTCGGCTTAC | 54793 |
| rs759552877 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453747 | ACAAAACAGGAGTAC[A/G]GGAACGTGGATAAAC | 54793 |
| rs759668802 | snp | A/T | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427640 | AAAATTCTCTATCCT[A/T]GTTATCAGGCAAAAA | 54793 |
| rs759688690 | snp | C/T | 1.80422e-05 | 0.00300346 | upstream-variant-2KB, missense, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458242 | AACAGGGTCACCCGC[C/T]TCATCGCGCTGCCCC | 54793 |
| rs759772477 | in-del | -/AC | 6.59223e-05 | 0.0057408 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440562 | CTTTCTAACACACAT[-/AC]ACACACACACCTACC | 54793 |
| rs759777034 | snp | A/G | 1.66081e-05 | 0.00288163 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435501 | AAGATCAGCACCACT[A/G]AAGTTCAAACCCTGA | 54793 |
| rs759804165 | in-del | -/GA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447192 | TAAGGCCTGGAGTTT[-/GA]GACCAGCCAGACCAA | 54793 |
| rs759858684 | in-del | -/A | 2.83748e-05 | 0.00376651 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458186 | CCGCCGCGCCCCCTC[-/A]CGCCCCCGTTACCTT | 54793 |
| rs759866787 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450481 | ATTTAAGTCTCTTAC[A/C]CTGTCATTAGGGTAA | 54793 |
| rs759922910 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452357 | ATATAAATTACTGCA[A/G]TGACTTTGAAAAACA | 54793 |
| rs759940875 | snp | A/C/G | 5.01126e-05 | 0.00500542 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439307 | GCCATCATTTACAAT[A/C/G]AGCTGTCCATGACGC | 54793 |
| rs760178983 | snp | A/G | 1.64732e-05 | 0.0028699 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460341 | AAGTTGAAGGTTTAG[A/G]CAGAGAGTTGTCCTC | 54793 |
| rs760231828 | snp | A/G | 1.73378e-05 | 0.00294425 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433285 | GCTTTTTTCCTTTAC[A/G]GTCTGCTTCCTTCGT | 54793 |
| rs760266907 | snp | G/T | 1.68838e-05 | 0.00290544 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436473 | CCAAAAAATCTTGCT[G/T]CTTCTAACACACCTA | 54793 |
| rs760315481 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448341 | CCAACACAGGCAAAT[G/T]CATAGAGAAAGAAAG | 54793 |
| rs760351981 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434609 | AGTAACTAAAATGCA[C/T]ATTTGGTAGATTTTG | 54793 |
| rs760425123 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460418 | GGGAACTGGGAAGAT[C/T]GTGACTCCTCAGAAG | 54793 |
| rs760533935 | snp | C/T | 1.64814e-05 | 0.00287061 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440562 | TCTTTCTAACACACA[C/T]ACACACACACCTACC | 54793 |
| rs760559007 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456033 | TCAAATACGTCCACC[A/G]CTAGTTACATTCATT | 54793 |
| rs760563400 | snp | A/C | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456664 | AAATAAAATTTAAAT[A/C]CAAGAATCTAATCTA | 54793 |
| rs760624126 | snp | C/T | 1.68386e-05 | 0.00290155 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440695 | ATGACATGTAGAAAA[C/T]AATACAAATATTAAG | 54793 |
| rs760630118 | snp | A/G | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427762 | AACGAATTATTGGGG[A/G]GGCAGTCTTTTCTTT | 54793 |
| rs760641483 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431373 | TACAGAACAGTGTAA[C/G]CACCGCAATTTGAAG | 54793 |
| rs760695399 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443616 | GTAGAGACAGACAGA[C/G]AAGAGTATGCACTTA | 54793 |
| rs760710633 | snp | A/G | 3.29728e-05 | 0.00406021 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432537 | CAGAGTTGCTCCTCT[A/G]AGGTTACAGTTCTTC | 54793 |
| rs760791971 | in-del | -/TTGAT | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427349 | AAAATATTCCAAGTC[-/TTGAT]TTATGATTGAACCCT | 54793 |
| rs760802287 | snp | C/G | 1.65012e-05 | 0.00287234 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460199 | AATCACGTTCATCTT[C/G]CTGGTGGGGTTATTT | 54793 |
| rs761040920 | in-del | -/C | 1.64972e-05 | 0.00287199 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439684 | AATTCAGGGAAAAAA[-/C]ATTGATTTCTCCATT | 54793 |
| rs761060009 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448654 | GCGCGGTGGCTCACG[C/T]CTGTAAAATCTGCAC | 54793 |
| rs761223555 | in-del | -/CTT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448909 | GACAAAGTGAGACTC[-/CTT]CTCCAAGAAAAAAAA | 54793 |
| rs761235772 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449998 | GAAGTCAAATGTGAC[C/G]AGATGATAGAAAAAA | 54793 |
| rs761297365 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460435 | TGACTCCTCAGAAGC[A/G]TGCCGAATTACCTCC | 54793 |
| rs761385696 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456214 | TATTCTTATAACCAG[A/G]AAACAAAAGCAGAAG | 54793 |
| rs761390573 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440901 | TCAGCGCCTGTGAAA[A/G]AAAAAGCAGAGAGAA | 54793 |
| rs761391575 | snp | A/G | 1.66424e-05 | 0.0028846 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439333 | GACGCAAGTAGTTCA[A/G]AATGGGTTCGAAGTA | 54793 |
| rs761439267 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459497 | GCATCCGCGCTGCCA[C/G]GGGGCTGTTTCTCCG | 54793 |
| rs761483217 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434814 | CATTGTTGGTCTGCA[C/T]ATATCCTCTAACTTC | 54793 |
| rs761563160 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445976 | CAATTCACCTTAAGC[C/T]CAAATGATTTAAATT | 54793 |
| rs761603264 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430696 | GAATCATCCCAAAAC[C/G]AGCCCCCGACTCTGA | 54793 |
| rs761633490 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430096 | TAAAACTCAGTTAAT[C/T]TCCGGAAAACTGATG | 54793 |
| rs761655044 | snp | C/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457134 | ATAGCCAACAAACCA[C/T]ACTCTGGTTCGAATT | 54793 |
| rs761699859 | snp | A/T | 0.00018167 | 0.009529 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432561 | GTTCTTCAACTTTGC[A/T]TTTTTTAAGGTAGCC | 54793 |
| rs761769724 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452961 | TGCTTGAGGCCAGGA[A/G]TTTGAGACCAGTCTG | 54793 |
| rs761869574 | snp | A/G | 6.06042e-05 | 0.0055044 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433485 | TTCATAATTTTGTTC[A/G]AATTAGCTCAAACAG | 54793 |
| rs761982209 | in-del | -/ACT | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427437 | AGTTGAAAGAACTAG[-/ACT]ACAATAGATAGTATT | 54793 |
| rs762036202 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439541 | TACAGAAGGTCAGGA[C/G]TTATAAAGTCAGCAC | 54793 |
| rs762068110 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433628 | ACATTTGAAAGAAAA[A/T]TTTTTTTAAAGAACT | 54793 |
| rs762163345 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449820 | CATTTTAAAGAGCAG[-/A]AAAAAAAAAAATGAA | 54793 |
| rs762251588 | snp | C/G | 1.79554e-05 | 0.00299623 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458266 | CTGCCCCCGCTGGGT[C/G]CTGAGTGAGCCGCCA | 54793 |
| rs762253052 | snp | A/G | 3.29641e-05 | 0.00405968 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436310 | GGATATTGGTGAATG[A/G]TCCTCCGGTGGTTGA | 54793 |
| rs762339587 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447656 | ACTTTTTTCTCTTGG[A/C]TCAGAAGGATGAAAG | 54793 |
| rs762429312 | snp | G/T | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459722 | TGGGGTCTGCTTTGG[G/T]GCCTGAACAGCAGTT | 54793 |
| rs762534837 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446382 | AAAGGTTCTTAACAG[C/T]GCCCCCTTTTCTTCC | 54793 |
| rs762562827 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449800 | GTAGTTCTATTAGAC[-/A]AGTGCCATTTTAAAG | 54793 |
| rs762574860 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456495 | CTTAGAATATGTTCA[A/T]CAGCTGAGCAGTGAA | 54793 |
| rs762620676 | snp | A/T | 1.75182e-05 | 0.00295953 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435350 | TTCTCTTGTAGCCTA[A/T]AATGATACTTACGTC | 54793 |
| rs762725048 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459245 | GGTGGAGGAGGCTGC[C/T]GGGCAGAGCGCAGGC | 54793 |
| rs762755345 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460440 | CCTCAGAAGCATGCC[A/G]AATTACCTCCTAATC | 54793 |
| rs762756803 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459335 | AGAGCGGCTCCCGGC[-/T]TGCGGGTGCTTTGCC | 54793 |
| rs762803093 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447246 | TAAAATACAAAAATC[A/C]GCCAGGTGTGGTGGT | 54793 |
| rs762915977 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452498 | TGCAGCATCTGAACC[A/C]CATTTCACCTGCAAA | 54793 |
| rs762999459 | snp | A/C | | | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439657 | GTTCTTTATTCACTA[A/C]AGTGCTCCTAAGAAT | 54793 |
| rs763001910 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450727 | TCAATCTCTTGACCT[C/T]GTGATCCAACCGCCT | 54793 |
| rs763021947 | in-del | -/CCTCACC | 1.64735e-05 | 0.00286993 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460353 | TAGACAGAGAGTTGT[-/CCTCACC]CCTACAATATGTCGT | 54793 |
| rs763048884 | in-del | -/CC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440850 | AGGTGATAAGGTAGT[-/CC]CACCAATACCAACAG | 54793 |
| rs763059815 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441497 | AATATTCCAAAACAT[A/G]CTAAAAGAAGTTTAT | 54793 |
| rs763091887 | snp | A/G | 3.33622e-05 | 0.00408412 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446102 | TTGAGGCACACTGTT[A/G]ACAGCTTATAAAAAG | 54793 |
| rs763243992 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444403 | ATTATCTGTTGCTTA[C/T]AGGAACTATTCCTTA | 54793 |
| rs763254266 | snp | C/G | 1.7081e-05 | 0.00292237 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433308 | TCCTTCGTAGAATAG[C/G]TATTTACAGAAAGGA | 54793 |
| rs763373632 | snp | C/T | 1.64727e-05 | 0.00286986 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460319 | TGTGATGATCTGCCT[C/T]CTTGTGAAGTTGAAG | 54793 |
| rs763402089 | snp | A/G | 1.64825e-05 | 0.00287071 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436317 | GGTGAATGATCCTCC[A/G]GTGGTTGAGAATTCT | 54793 |
| rs763495676 | snp | G/T | 1.65578e-05 | 0.00287726 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436439 | TGCCACTTCTAGGTG[G/T]TCAATCAATGAGTCA | 54793 |
| rs763652903 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433755 | CACCTCTATCTCTAT[A/T]TTTATAAACATACCT | 54793 |
| rs763772307 | snp | A/G | 1.70945e-05 | 0.00292351 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436480 | ATCTTGCTTCTTCTA[A/G]CACACCTATCAGAAC | 54793 |
| rs763773214 | in-del | -/TC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435244 | CAACATAATAAATTA[-/TC]TGTTTTCAAGTAAAA | 54793 |
| rs763791109 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453957 | GCCTTCAGAGGCAGA[A/G]GTTCAGATAAATTTT | 54793 |
| rs763924988 | snp | C/T | 1.64798e-05 | 0.00287047 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440566 | TCTAACACACATACA[C/T]ACACACCTACCGTGT | 54793 |
| rs763965978 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437176 | ATACAGGGTCCACAT[A/T]TCCCCTTCAAGAGGC | 54793 |
| rs763983782 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428142 | TTTTAGGTTATTTCT[A/G]CAGAGGTACCTTTAA | 54793 |
| rs764013251 | snp | A/G | 1.70691e-05 | 0.00292134 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440711 | AATACAAATATTAAG[A/G]TTGGGGATTCTGGGA | 54793 |
| rs764017339 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439895 | CCTTTGCTTTAAATA[C/G]TTGTCTGTCTATCCT | 54793 |
| rs764101108 | snp | A/T | 1.64985e-05 | 0.0028721 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432554 | GGTTACAGTTCTTCA[A/T]CTTTGCATTTTTTAA | 54793 |
| rs764113302 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449884 | GCTTTCCCATGACAT[A/T]GGAACCCAAAGTAAC | 54793 |
| rs764222717 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435137 | AGATTTAATTTCTTA[-/T]TAGTTACTAAACCTT | 54793 |
| rs764267124 | in-del | -/GTC | 1.64732e-05 | 0.0028699 | cds-indel, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460370 | TCACCCCTACAATAT[-/GTC]GTCCGTTTCAGGAAA | 54793 |
| rs764276416 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438359 | ATATAAAGTTTGTTA[C/T]AGCAACACTAAAAGT | 54793 |
| rs764287686 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450864 | TTTGTAATAAGGGGG[C/G]AAGTTTTAATTTATT | 54793 |
| rs764387832 | snp | A/G | 4.84743e-05 | 0.00492288 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458168 | CTCGCCCCGACCCCC[A/G]GCCCGCCGCGCCCCC | 54793 |
| rs764398763 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439451 | CCCCATAAACAAAAA[A/C]TAAAGTCAGAAATGT | 54793 |
| rs764479888 | snp | A/G | 1.67525e-05 | 0.00289413 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435382 | AGCACTGATCCAGAG[A/G]GATCAGCTCGTTCAA | 54793 |
| rs764488441 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446433 | GTGCCTAATATTGCC[A/G]ACTCCTCAACTAGAA | 54793 |
| rs764519395 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443516 | GTGTTTGTATGCAGT[A/G]GACCAATTAAGTGAC | 54793 |
| rs764628839 | snp | C/G | 1.79693e-05 | 0.00299739 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458257 | CTCATCGCGCTGCCC[C/G]CGCTGGGTCCTGAGT | 54793 |
| rs764666541 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460436 | GACTCCTCAGAAGCA[C/T]GCCGAATTACCTCCT | 54793 |
| rs764679542 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459542 | ACTTTGTTCGGCTTA[C/G]CCTGCAGCACAGAAT | 54793 |
| rs764723663 | snp | C/G | 1.77055e-05 | 0.00297531 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435560 | CTAAATCGTCTGTTT[C/G]TATTAAATTTAATTA | 54793 |
| rs764760245 | snp | A/G | 3.32779e-05 | 0.00407895 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439343 | GTTCAAAATGGGTTC[A/G]AAGTACTCAGGACTT | 54793 |
| rs764846430 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445352 | AACTGCAAAGCAGTA[C/T]ATTATACTGAAAGGT | 54793 |
| rs764850696 | snp | A/G | 3.29614e-05 | 0.00405951 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439561 | AAAGTCAGCACAGAT[A/G]TAAAACAGGTAAGAT | 54793 |
| rs764926465 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455222 | AGAGCAAAACTCCGT[C/T]TCAAAAAATAATAAT | 54793 |
| rs764936315 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456238 | GCAGAAGCGAGGTAA[A/G]GGAGATAAAGTAAGT | 54793 |
| rs765087817 | snp | A/G | 0.000499729 | 0.0157992 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433299 | CAGTCTGCTTCCTTC[A/G]TAGAATAGGTATTTA | 54793 |
| rs765179276 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452331 | GGAAGATTTATGCAA[A/T]GGTGGTGGGAATATA | 54793 |
| rs765181835 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25436905 | TCCATTATCTTTCAA[A/C]TGAGAAGACCTCAAT | 54793 |
| rs765236863 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430697 | AATCATCCCAAAACC[A/G]GCCCCCGACTCTGAT | 54793 |
| rs765308157 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438438 | CAGGCTGATTCTGAT[A/G]TGTTCAGCATGTAAT | 54793 |
| rs765309414 | in-del | -/TATTCATG | 3.30972e-05 | 0.00406786 | intron-variant | KCTD9 | GRCh38.p7 | 8:25429991 | GCAAGATGAAAACAA[-/TATTCATG]TAATTCATGTGGAAA | 54793 |
| rs765348995 | snp | A/G | 1.76468e-05 | 0.00297037 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440725 | GATTGGGGATTCTGG[A/G]AAGATGGTAATGGCA | 54793 |
| rs765489579 | in-del | -/T | 3.84231e-05 | 0.00438293 | upstream-variant-2KB, frameshift-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458209 | GTTACCTTTCCGTTC[-/T]TGGGGCTGCCGTTCA | 54793 |
| rs765557816 | snp | A/G | 1.67158e-05 | 0.00289096 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446092 | CACCAAGAAGTTGAG[A/G]CACACTGTTGACAGC | 54793 |
| rs765576321 | snp | C/T | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459755 | CTCCATTTCTTTCTG[C/T]TTAATTTGGCTTTAA | 54793 |
| rs765635481 | snp | A/G/T | 3.59107e-05 | 0.00423725 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458272 | CCGCTGGGTCCTGAG[A/G/T]GAGCCGCCACCCTCC | 54793 |
| rs765731612 | snp | A/G | 4.96266e-05 | 0.00498105 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436200 | ATTCATAGATTTGCT[A/G]ATAGAAATAATTGAT | 54793 |
| rs765731701 | snp | G/T | 4.94947e-05 | 0.00497443 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460204 | CGTTCATCTTGCTGG[G/T]GGGGTTATTTTTCAT | 54793 |
| rs765813322 | snp | C/T | 1.64819e-05 | 0.00287066 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436313 | TATTGGTGAATGATC[C/T]TCCGGTGGTTGAGAA | 54793 |
| rs765817332 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432168 | CAAAAAACATATGGT[A/T]CCAATTTCAAATAGA | 54793 |
| rs765908668 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447663 | TCTCTTGGATCAGAA[A/G]GATGAAAGCCAGAAG | 54793 |
| rs765936197 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450007 | TGTGACCAGATGATA[-/G]AAAAAAACCACACAT | 54793 |
| rs766041740 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452914 | CTCATGCCTGTAGTC[-/G]GCAGCACCTTGGGAG | 54793 |
| rs766203932 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431790 | ATGAAAAAACATTAA[C/T]AGCAAGCTAAATTTT | 54793 |
| rs766241108 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431415 | TTTGTCTTGAGATCA[C/T]GGAGCAATAAGATAG | 54793 |
| rs766277041 | snp | G/T | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456869 | TAAAAAGGTCAACCA[G/T]AAGTTTGTTTTTGAG | 54793 |
| rs766305809 | snp | C/T | 3.33717e-05 | 0.0040847 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439383 | AAGAAAGCTCCTCTA[C/T]GATCTTGCTTATTTC | 54793 |
| rs766384185 | snp | A/T | 4.95062e-05 | 0.004975 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444266 | TTTTTTTTTGGCAGA[A/T]AAAATTGGCTTTTAA | 54793 |
| rs766474390 | snp | C/T | 1.66796e-05 | 0.00288782 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446104 | GAGGCACACTGTTGA[C/T]AGCTTATAAAAAGGT | 54793 |
| rs766485050 | snp | A/C | 1.691e-05 | 0.0029077 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433320 | TAGGTATTTACAGAA[A/C]GGATCTCACCTTCTA | 54793 |
| rs766527342 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441705 | AATAGCTTGAAAAAT[A/T]AAAAAGAAATGGTCA | 54793 |
| rs766690030 | snp | C/T | 1.74461e-05 | 0.00295343 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435353 | TCTTGTAGCCTAAAA[C/T]GATACTTACGTCAAG | 54793 |
| rs766800511 | in-del | -/AAACAAACA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439709 | TCCATTTGTCTTTAT[-/AAACAAACA]TATTTAAGTCAAGAG | 54793 |
| rs766849106 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448715 | AGCTCAGGAGTTCGA[C/G]ACCAGCTTGGGCAAC | 54793 |
| rs766853119 | snp | A/G | 1.65699e-05 | 0.00287831 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436442 | CACTTCTAGGTGTTC[A/G]ATCAATGAGTCAATA | 54793 |
| rs766927872 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459731 | CTTTGGTGCCTGAAC[A/G]GCAGTTTTCTCCATT | 54793 |
| rs766982101 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434862 | TGTTATAAATACATA[C/G]ATATACATATATATA | 54793 |
| rs766994410 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434136 | ACAAAGTCTCACTCC[A/G]TCACCCAGGATGGAG | 54793 |
| rs767016985 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447513 | TAAGGCTGGTCCTCT[C/G]TCCACCAGTGACTGG | 54793 |
| rs767060168 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432477 | AGTCTAGAGTAATAA[A/G]AATTCTTAAAGTGTT | 54793 |
| rs767134276 | snp | A/G | 1.64727e-05 | 0.00286986 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460325 | GATCTGCCTCCTTGT[A/G]AAGTTGAAGGTTTAG | 54793 |
| rs767170295 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460222 | GGTTATTTTTCATTG[C/T]TTTTCTTCACCTCTT | 54793 |
| rs767201331 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432039 | TGGATAGTGCTGATA[C/T]AGACCTATCAACAGC | 54793 |
| rs767210342 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458405 | ACACGCACGCACTCT[-/G]TCCCACACCCAAGGT | 54793 |
| rs767334387 | snp | G/T | 1.65045e-05 | 0.00287263 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440535 | AGGGTACACAGTGCT[G/T]CTTTTGCATTCTCTT | 54793 |
| rs767335490 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436322 | ATGATCCTCCGGTGG[C/T]TGAGAATTCTTAAAA | 54793 |
| rs767374990 | snp | A/G | 1.64803e-05 | 0.00287052 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439575 | TATAAAACAGGTAAG[A/G]TGAAATGTGAAAACA | 54793 |
| rs767588265 | snp | C/T | 1.71223e-05 | 0.00292589 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435365 | AAATGATACTTACGT[C/T]AAGCACTGATCCAGA | 54793 |
| rs767707228 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449553 | CTTCCATATGATTGA[C/G]TTGGTTTTTCTGTGG | 54793 |
| rs767746508 | snp | C/T | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427749 | CACAAACAAATTAAA[C/T]GAATTATTGGGGAGG | 54793 |
| rs767884128 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435784 | TAAAGAGGGATCCCT[A/G]TTAGTCCTATACCTG | 54793 |
| rs767979493 | snp | A/C | 1.65203e-05 | 0.002874 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446140 | TTACCTGATCAAAGC[A/C]ATATCATCAATCAGT | 54793 |
| rs768095259 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451595 | TGTCTATTAAAGTTC[A/C]TGATGTCTGTATTAT | 54793 |
| rs768121497 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435715 | AAAAGAAACTCTATC[-/A]ATATATACATTAGAA | 54793 |
| rs768125871 | snp | A/G | | | stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436279 | TTGCTAGCAAAAATC[A/G]GACAAATTCCTTTCG | 54793 |
| rs768127748 | snp | A/C | 0.000351609 | 0.0132545 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458165 | GCCCTCGCCCCGACC[A/C]CCGGCCCGCCGCGCC | 54793 |
| rs768265391 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460425 | GGGAAGATTGTGACT[C/T]CTCAGAAGCATGCCG | 54793 |
| rs768364318 | in-del | -/C | 9.60015e-05 | 0.00692759 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439229 | AAAATCTTAAACTTA[-/C]AAAAATGTGAGTAGT | 54793 |
| rs768417208 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25436902 | GGTTCCATTATCTTT[C/G]AAATGAGAAGACCTC | 54793 |
| rs768433600 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434648 | CCTGATACACAGCTT[C/T]ATGGAAAAATAAGCT | 54793 |
| rs768624898 | snp | A/C | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436293 | CGGACAAATTCCTTT[A/C]GGGATATTGGTGAAT | 54793 |
| rs768694950 | snp | A/G | 1.81513e-05 | 0.00301253 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444384 | AAATCTAAAAATCAC[A/G]TTAATTATCTGTTGC | 54793 |
| rs768781688 | snp | A/G | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460288 | ACCAAGGAGTCTGCA[A/G]TGAATAATGCTGGTA | 54793 |
| rs768784561 | snp | C/G | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446225 | ACAGAAAGCAAATCA[C/G]ATAAAGTTCCATATA | 54793 |
| rs768784633 | snp | C/T | 1.72946e-05 | 0.00294058 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433292 | TCCTTTACAGTCTGC[C/T]TCCTTCGTAGAATAG | 54793 |
| rs768796719 | snp | C/T | 2.07149e-05 | 0.00321823 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436536 | TTAGTGAATGTATTA[C/T]ATTCATTTTGAATTT | 54793 |
| rs768859801 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453157 | CAGGAGGTCAGCCGA[G/T]ACCAGCCTGACCAAC | 54793 |
| rs768898266 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452170 | CTTTTAGTCAAATAC[A/C]TTTTAAATATTTACA | 54793 |
| rs768941293 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431428 | CACGGAGCAATAAGA[A/T]AGAGATTCCACTTAA | 54793 |
| rs769018308 | snp | A/G | 0.000131791 | 0.00811655 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440627 | TGTCAGCCAGTCTGT[A/G]TGGAATCCTAACAAT | 54793 |
| rs769108012 | snp | C/T | 1.66607e-05 | 0.00288619 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430021 | TGTGGAAATTTCAGG[C/T]CTTATCTATTTCTGC | 54793 |
| rs769231624 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451448 | AATCATAAAATGATA[A/G]TGCTTACAAAGGTCA | 54793 |
| rs769280921 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449832 | GCAGAAAAAAAAAAA[A/T]GAAGAAAAAAAAACA | 54793 |
| rs769567428 | snp | A/G | 1.79245e-05 | 0.00299365 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435319 | TGAGACTGTTCAATA[A/G]ACTAAACATTTAATT | 54793 |
| rs769616810 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431665 | TAACAAACAATAAAT[A/T]ATTGTGCTCGTGATA | 54793 |
| rs769632762 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439472 | CAGAAATGTATGAGG[-/A]AAAAAATTGCTAAAT | 54793 |
| rs769725096 | snp | A/G | 1.89766e-05 | 0.00308025 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458211 | TACCTTTCCGTTCTT[A/G]GGGCTGCCGTTCAGG | 54793 |
| rs769806926 | snp | A/G | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435437 | GTGCAAGATTACAGC[A/G]GCTTAAATTGGCCAT | 54793 |
| rs769915841 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432928 | AATATACAAGTAAAC[A/C]AAGTGATCAGTCACA | 54793 |
| rs769982280 | in-del | -/AAATA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442012 | CTGTCTCAAAAAAAT[-/AAATA]AAATAAAAAGAAAGG | 54793 |
| rs770006390 | snp | A/T | 1.77979e-05 | 0.00298306 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439255 | GTAGTTACATAATTA[A/T]ATTGAAAGTCTAAAT | 54793 |
| rs770094344 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453995 | CTCCAACTCTAACAA[C/T]GTAATGGATTCAAAC | 54793 |
| rs770128736 | snp | A/G | 1.6727e-05 | 0.00289193 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432663 | CACATTCTGGGAGTA[A/G]TTTAACTTAAAAATA | 54793 |
| rs770149938 | in-del | -/TTTAC | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427860 | GTTTAAAGAAATAAA[-/TTTAC]TTTACTTTAATGGTA | 54793 |
| rs770224516 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429004 | TTGAAGTATCTTCCT[A/G]TGCTTGTGATGACTG | 54793 |
| rs770439812 | snp | A/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440659 | CCTCAGGAGGCTTAG[A/T]ATCTGTCTGAGGATC | 54793 |
| rs770477139 | snp | A/C | 1.65542e-05 | 0.00287695 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439714 | TTGTCTTTATAAACA[A/C]ACATATTTAAGTCAA | 54793 |
| rs770487778 | snp | A/C | 1.65067e-05 | 0.00287282 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436410 | GGCTAATGTAAAAAC[A/C]GGCTTACCTTTATTG | 54793 |
| rs770492177 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460395 | TCAGGAAATGCCTCT[G/T]TCATTTTGGGAACTG | 54793 |
| rs770584707 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447570 | TAAATACAGTAAATG[A/G]AGGACATGGAAAAAG | 54793 |
| rs770610831 | snp | A/G | 1.64996e-05 | 0.0028722 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432470 | CTTAGTAAGTCTAGA[A/G]TAATAAAAATTCTTA | 54793 |
| rs770644489 | snp | A/G/T | 4.95432e-05 | 0.0049769 | synonymous-codon, stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435470 | TGAAGTTAATGTATC[A/G/T]AAGGTCCAAACGAGA | 54793 |
| rs770727321 | snp | A/G | 1.79716e-05 | 0.00299757 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458294 | CCACCCTCCCACCTG[A/G]TCCTCCTCCCACCTT | 54793 |
| rs771030504 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447107 | GGAATAAAAACTAGG[-/T]TAAGGGTCGGGCGCA | 54793 |
| rs771098519 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453141 | CTGAGGCGGGCAGAT[-/C]CAGGAGGTCAGCCGA | 54793 |
| rs771211756 | snp | C/G | 1.82553e-05 | 0.00302115 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458232 | GCCGTTCAGGAACAG[C/G]GTCACCCGCCTCATC | 54793 |
| rs771249444 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429126 | TCATTTGTAAGTGTT[C/G]TAGTGATAGGTAAGT | 54793 |
| rs771277062 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444774 | ATAGCTGGAAGTAAC[C/T]CTACTGTCAGTGTTT | 54793 |
| rs771288216 | in-del | -/GAAGTTGAG | 3.34538e-05 | 0.00408971 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446082 | ACAGCATAGCACCAA[-/GAAGTTGAG]GAAGTTGAGGCACAC | 54793 |
| rs771292978 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443123 | TACATTATATACAAA[C/T]TTTATCTCTACCTAT | 54793 |
| rs771295053 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455784 | TCACATGTGAAGGCC[A/G]TCCCTTCTTACAGGA | 54793 |
| rs771331762 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460404 | GCCTCTTTCATTTTG[A/G]GAACTGGGAAGATTG | 54793 |
| rs771408619 | snp | A/G | 1.69654e-05 | 0.00291246 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439453 | CCATAAACAAAAAAT[A/G]AAGTCAGAAATGTAT | 54793 |
| rs771456281 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450395 | CTGGCTTACAGCAGG[A/T]CTTTGACAAATATTT | 54793 |
| rs771514229 | snp | C/T | 1.68252e-05 | 0.0029004 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439291 | CACCCAATAAATTAA[C/T]GCCATCATTTACAAT | 54793 |
| rs771578146 | snp | A/G | 1.6793e-05 | 0.00289763 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432678 | GTTTAACTTAAAAAT[A/G]TAGTTATCTACCTTC | 54793 |
| rs771609035 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433617 | AAGAACTGGGAACAT[G/T]TGAAAGAAAAATTTT | 54793 |
| rs771636183 | in-del | -/TTT/TTTT | 0.000171751 | 0.00926557 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444261 | TTTTTTTTTTTTTGG[-/TTT/TTTT]CAGATAAAATTGGCT | 54793 |
| rs771655189 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460335 | CTTGTGAAGTTGAAG[A/G]TTTAGACAGAGAGTT | 54793 |
| rs771817310 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431268 | TAATAGATTTTTCCA[-/T]TCCCTAGCCCTAGTA | 54793 |
| rs771853250 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448315 | CTATGATACCACTCA[C/T]ATGAAAGTACCCAAC | 54793 |
| rs771870220 | snp | C/T | 0.000197847 | 0.00994406 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436365 | AATTAGTGGAGTCTT[C/T]TGGGAGATAGCTACA | 54793 |
| rs771878704 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455866 | GATCGGAAAAATCAA[A/G]TTTTCACATTATTTT | 54793 |
| rs771942463 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434481 | ACAAAGATGCCTCTC[A/G]ACATTTCACTATTTA | 54793 |
| rs772147084 | snp | A/G | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456943 | CAACATACGTTTTAG[A/G]TAACAGGTAGTAGCT | 54793 |
| rs772176724 | in-del | -/TT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456095 | CACAGCACCTTGGAA[-/TT]GAATTCTGTGCCTCT | 54793 |
| rs772245998 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458619 | AGACGCTGAAGGCTA[A/G]TAGACGGGAAGGGGC | 54793 |
| rs772314605 | snp | A/G | 1.65089e-05 | 0.00287301 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460190 | ACGTGATCGAATCAC[A/G]TTCATCTTGCTGGTG | 54793 |
| rs772348665 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436269 | TTGGTTGGAGTTGCT[A/G]GCAAAAATCGGACAA | 54793 |
| rs772349229 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445798 | GATTAACAAGCAGGC[A/G]CATATAAAAGTGAAG | 54793 |
| rs772413675 | snp | A/G | 6.59446e-05 | 0.00574177 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439669 | CTAAAGTGCTCCTAA[A/G]AATTCAGGGAAAAAA | 54793 |
| rs772435033 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429769 | TCCTTACAGTGTTAT[G/T]TCTTCTAGACAACTG | 54793 |
| rs772497075 | in-del | -/AAC | 4.94352e-05 | 0.00497143 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439587 | AAGATGAAATGTGAA[-/AAC]AACGTGTTACACTCA | 54793 |
| rs772499398 | snp | C/T | 1.65312e-05 | 0.00287495 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429829 | AAACATTTTCATCTT[C/T]TACATCTTCCTCCAG | 54793 |
| rs772724868 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438976 | AGGAAACAACAAAAT[C/G]CTTTAAAGTCACTTG | 54793 |
| rs772753941 | snp | A/G | 1.64821e-05 | 0.00287067 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439563 | AGTCAGCACAGATAT[A/G]AAACAGGTAAGATGA | 54793 |
| rs772834037 | snp | C/T | 0.000164989 | 0.00908116 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439686 | ATTCAGGGAAAAAAA[C/T]TGATTTCTCCATTTG | 54793 |
| rs772863230 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445495 | CAGGCAAAGCAATGA[-/T]TAACATAAGTGGCAT | 54793 |
| rs772926933 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430701 | ATCCCAAAACCAGCC[C/G]CCGACTCTGATCTGT | 54793 |
| rs772959065 | snp | C/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457265 | AGGCAGCAGAGTATT[C/T]TGGCAACCAACACAG | 54793 |
| rs773014729 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446074 | TTAAGGGAAACAGCA[C/T]AGCACCAAGAAGTTG | 54793 |
| rs773104197 | snp | A/C | 1.78302e-05 | 0.00298577 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435337 | TAAACATTTAATTTT[A/C]TCTTGTAGCCTAAAA | 54793 |
| rs773288675 | in-del | -/AA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440429 | CATGTTTTTTTCTTC[-/AA]AAAAAGTTATAAAAA | 54793 |
| rs773316594 | snp | C/T | 1.6691e-05 | 0.00288881 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446098 | GAAGTTGAGGCACAC[C/T]GTTGACAGCTTATAA | 54793 |
| rs773357647 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441460 | CCAGAAATACCCACA[A/G]AATAGATCAAAATTA | 54793 |
| rs773483472 | snp | C/T | | | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436433 | CTTTATTGCCACTTC[C/T]AGGTGTTCAATCAAT | 54793 |
| rs773628047 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448642 | GAGTAGGGCTGGGCG[C/T]GGTGGCTCACGCCTG | 54793 |
| rs773647677 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449948 | TGTTTTATTTAGAGG[A/G]TTGGGATGTTGCCAT | 54793 |
| rs773658581 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442991 | GTAAGACAGAAGAGG[A/G]TAAGTAAAAACCTTA | 54793 |
| rs773692863 | snp | C/T | 6.60633e-05 | 0.00574694 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440528 | AGAACAAAGGGTACA[C/T]AGTGCTTCTTTTGCA | 54793 |
| rs773748570 | in-del | -/A | 1.64928e-05 | 0.00287161 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439678 | CCTAAGAATTCAGGG[-/A]AAAAAAATTGATTTC | 54793 |
| rs773750069 | snp | C/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457499 | TCCGCAAAGGCCTAA[C/T]ACAGCAAAGGCGACT | 54793 |
| rs773839514 | snp | A/G | 3.30196e-05 | 0.00406309 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436411 | GCTAATGTAAAAACA[A/G]GCTTACCTTTATTGC | 54793 |
| rs773898479 | snp | C/T | 6.59174e-05 | 0.00574059 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429907 | GCATCTCTTCAAATA[C/T]AGCTCCCTTCACGTT | 54793 |
| rs773959369 | snp | C/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440663 | AGGAGGCTTAGAATC[C/T]GTCTGAGGATCTAGA | 54793 |
| rs774046221 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432474 | GTAAGTCTAGAGTAA[C/T]AAAAATTCTTAAAGT | 54793 |
| rs774062024 | in-del | -/AAAG | 3.38418e-05 | 0.00411336 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439426 | TGTCACCATTATAAT[-/AAAG]AAAGTCCCCCATAAA | 54793 |
| rs774163758 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431953 | CAAGCGCTCAATAGC[C/T]ATATATGGGTGGTAG | 54793 |
| rs774181796 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436253 | GCATCGCAGTTCTGA[C/T]TTGGTTGGAGTTGCT | 54793 |
| rs774200731 | snp | C/T | 0.000131776 | 0.00811608 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460266 | TTCAAAAGACAAGCC[C/T]CCTGAAACCAAGGAG | 54793 |
| rs774262851 | in-del | -/TAG | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440239 | AATTTTTTGTATTTT[-/TAG]TAGAGACGGGGTTTC | 54793 |
| rs774453649 | snp | A/C/T | 0.000419341 | 0.0144744 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458163 | CCGCCCTCGCCCCGA[A/C/T]CCCCGGCCCGCCGCG | 54793 |
| rs774471297 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453595 | GAGGCGGAGGTTGTA[C/T]TGAGCCAGAGATCAT | 54793 |
| rs774543106 | snp | C/T | 1.73102e-05 | 0.0029419 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435359 | AGCCTAAAATGATAC[C/T]TACGTCAAGCACTGA | 54793 |
| rs774543305 | snp | C/T | 1.82257e-05 | 0.0030187 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458235 | GTTCAGGAACAGGGT[C/T]ACCCGCCTCATCGCG | 54793 |
| rs774598023 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454693 | AAAGATTCCAGTGAT[C/T]AGAACTAAGGCCTTC | 54793 |
| rs774603158 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429738 | CATAATCCTCTAAAT[A/G]TTTTTTTTTTAAATT | 54793 |
| rs774610510 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456010 | AATGCATAGCCCTCT[C/T]TCCAACGTCAAATAC | 54793 |
| rs774771004 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450439 | TGTTGAAGTAGGACA[A/C]ACCTTTTTTGTGTGA | 54793 |
| rs774774478 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449469 | TATTATGCTTAATAC[A/T]TAATGTAATATTATA | 54793 |
| rs774824318 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432530 | TTCCTGCCAGAGTTG[C/G]TCCTCTGAGGTTACA | 54793 |
| rs775093429 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449833 | CAGAAAAAAAAAAAT[G/T]AAGAAAAAAAAACAC | 54793 |
| rs775115836 | snp | C/T | 1.67899e-05 | 0.00289736 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432679 | TTTAACTTAAAAATA[C/T]AGTTATCTACCTTCA | 54793 |
| rs775147224 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454989 | CTAGCACTTTGGGAA[A/G]CCAAGGCAGGTGGAT | 54793 |
| rs775151551 | snp | A/C | 1.64741e-05 | 0.00286998 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460354 | AGACAGAGAGTTGTC[A/C]TCACCCCTACAATAT | 54793 |
| rs775327482 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443517 | TGTTTGTATGCAGTG[G/T]ACCAATTAAGTGACC | 54793 |
| rs775330273 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449044 | GGGACAAAGCGAAGC[A/G]AAATACAGTACCTAG | 54793 |
| rs775394985 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442705 | AGTGTATAAAGGGAG[A/C]CACTATAATATACAA | 54793 |
| rs775428475 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437124 | CAATTGTAAAACAAA[C/T]GTCATCCAAGGTACA | 54793 |
| rs775470585 | snp | C/T | 1.6507e-05 | 0.00287284 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460193 | TGATCGAATCACGTT[C/T]ATCTTGCTGGTGGGG | 54793 |
| rs775590502 | snp | A/G | 3.5966e-05 | 0.00424049 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458253 | CCGCCTCATCGCGCT[A/G]CCCCCGCTGGGTCCT | 54793 |
| rs775658289 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444983 | GACGTTTTTATTTCC[C/T]ATAGGACATCACAGG | 54793 |
| rs775677959 | snp | C/T | 4.94434e-05 | 0.00497184 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436289 | AAATCGGACAAATTC[C/T]TTTCGGGATATTGGT | 54793 |
| rs775679346 | snp | G/T | 1.64814e-05 | 0.00287061 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439558 | TATAAAGTCAGCACA[G/T]ATATAAAACAGGTAA | 54793 |
| rs775679771 | snp | A/T | 9.885e-05 | 0.0070296 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439600 | AAAACAACGTGTTAC[A/T]CTCACCTTTGTCCTT | 54793 |
| rs775708799 | in-del | -/AG | 0.00016472 | 0.00907375 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460343 | GTTGAAGGTTTAGAC[-/AG]AGAGTTGTCCTCACC | 54793 |
| rs775766233 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437699 | AAAAAAATACAAATA[C/T]TAGCTGGGCATCATG | 54793 |
| rs775825070 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451964 | CTAATCTGGCTGTCT[A/G]CCTGGATCCTAAAGG | 54793 |
| rs775857928 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450640 | CCAACATGGTAAAAC[C/T]GTGCCACCACGCCCA | 54793 |
| rs775912413 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430592 | GGGCTCCCACTGATT[A/C]TACATTATGGTGAGT | 54793 |
| rs776023534 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439134 | CACTCATATACATGT[A/G]AAAACATCTAGTTTA | 54793 |
| rs776062971 | snp | G/T | 1.65168e-05 | 0.00287369 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429834 | TTTTCATCTTTTACA[G/T]CTTCCTCCAGCCCCT | 54793 |
| rs776123719 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445906 | CATAGCTATATATGA[A/T]CTATGCAGAAAGACT | 54793 |
| rs776188176 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460426 | GGAAGATTGTGACTC[A/C]TCAGAAGCATGCCGA | 54793 |
| rs776217657 | snp | A/G | 2.79256e-05 | 0.00373658 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433481 | AAGGTTCATAATTTT[A/G]TTCAAATTAGCTCAA | 54793 |
| rs776286481 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445245 | ATCTGTTTTCATTAA[A/C]AAAACCCAACTAGCT | 54793 |
| rs776360829 | snp | C/G | 1.66896e-05 | 0.00288869 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439310 | ATCATTTACAATGAG[C/G]TGTCCATGACGCAAG | 54793 |
| rs776403944 | snp | C/G | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457107 | TCTCTAAGACCAAAA[C/G]AACATAAAATTATAG | 54793 |
| rs776422260 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456133 | CTTCCCCAGGCTTCA[C/T]AGTCTCACAGTCTGG | 54793 |
| rs776422899 | snp | A/G | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446229 | AAAGCAAATCAGATA[A/G]AGTTCCATATACAGC | 54793 |
| rs776513263 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431493 | GAAGGGTGACTAAAC[A/G]TAACCTGTTAGGAGA | 54793 |
| rs776533003 | snp | A/C/G | 0.000133803 | 0.00817832 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446082 | AACAGCATAGCACCA[A/C/G]GAAGTTGAGGCACAC | 54793 |
| rs776620194 | snp | C/G | 1.64969e-05 | 0.00287196 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436387 | ATAGCTACAATGAAT[C/G]TAACACTGGCTAATG | 54793 |
| rs776700669 | snp | C/T | 1.72913e-05 | 0.0029403 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433294 | CTTTACAGTCTGCTT[C/T]CTTCGTAGAATAGGT | 54793 |
| rs776736115 | snp | A/G | 1.64814e-05 | 0.00287061 | stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436294 | GGACAAATTCCTTTC[A/G]GGATATTGGTGAATG | 54793 |
| rs776755328 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452228 | ATTTAAAAAAAAGAT[A/G]AGATAATTAACTCTA | 54793 |
| rs776776602 | in-del | -/TAGA | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427433 | TATAGTTGAAAGAAC[-/TAGA]TAGACTACAATAGAT | 54793 |
| rs776816982 | snp | A/G | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460290 | CAAGGAGTCTGCAAT[A/G]AATAATGCTGGTATG | 54793 |
| rs776917013 | in-del | -/TCTT | 3.29777e-05 | 0.00406051 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440547 | GCTTCTTTTGCATTC[-/TCTT]TCTAACACACATACA | 54793 |
| rs776998647 | snp | C/T | 1.6501e-05 | 0.00287232 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432460 | GCATGAGATGCTTAG[C/T]AAGTCTAGAGTAATA | 54793 |
| rs777043287 | in-del | -/TAATAC | 1.67144e-05 | 0.00289084 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446286 | TATGAACAATTTCTT[-/TAATAC]ATGTTATCCCCCATA | 54793 |
| rs777234420 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459593 | GCTCTGGGTGACCAG[C/G]AGTGCATCCGGACCT | 54793 |
| rs777277910 | snp | A/G | 3.29875e-05 | 0.00406112 | splice-donor-variant | KCTD9 | GRCh38.p7 | 8:25436233 | AAAAGCCTGCTAATT[A/G]CCTGGCATCGCAGTT | 54793 |
| rs777358701 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441046 | TGCAAGTAGTTTGCA[C/G]TAAGATCTTATAGGG | 54793 |
| rs777447404 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432877 | TTCATAATATGCCTC[C/T]ACAGGTTTATGATAA | 54793 |
| rs777515719 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449437 | AAAAATAGATGCAAG[C/T]TGAATGCACCTGCCT | 54793 |
| rs777655495 | snp | A/G | 1.65685e-05 | 0.00287819 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429809 | AGAAAGAAAAGTGAT[A/G]AGGAAAACATTTTCA | 54793 |
| rs777656291 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433033 | AAATTTTTCCTTTTG[A/G]TCAGTGTAAGAATAT | 54793 |
| rs777660411 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448850 | AACCCGGGAGGCAGA[A/G]GTTGCAGTTAGCTGA | 54793 |
| rs777782917 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434212 | TCAAGTGATTCTCGT[C/G]CCTCAGCCTCCTGAG | 54793 |
| rs777941244 | snp | A/T | 1.67295e-05 | 0.00289214 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432664 | ACATTCTGGGAGTAG[A/T]TTAACTTAAAAATAT | 54793 |
| rs777941561 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444589 | ATCTCCTTACACAAA[C/T]GATGTTGAGTTCAGC | 54793 |
| rs778020774 | snp | A/C | 1.69502e-05 | 0.00291115 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439438 | AATAAAGAAAGTCCC[A/C]CATAAACAAAAAATA | 54793 |
| rs778134298 | snp | A/G/T | 4.94697e-05 | 0.00497321 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446194 | GGTGGCTTTTATGCC[A/G/T]AGTTTACTGCTGGCC | 54793 |
| rs778213870 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429069 | GAATTGCTTGATCTG[A/G]TGTTGAGTGGAACTT | 54793 |
| rs778224335 | snp | C/T | 2.01623e-05 | 0.00317502 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433439 | GAGATTCGCACACTG[C/T]AAAGAAAAGAGAAAA | 54793 |
| rs778228972 | snp | A/C | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456573 | TTACGTTGTAACATA[A/C]ACATATTTATATTTA | 54793 |
| rs778416333 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445504 | GCAATGATAACATAA[A/G]TGGCATAGTCAATAC | 54793 |
| rs778426185 | snp | C/T | 1.76664e-05 | 0.00297202 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444363 | AAATTTAAAAAGCTA[C/T]CATCAAAATCTAAAA | 54793 |
| rs778638477 | snp | A/C | 1.79845e-05 | 0.00299865 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458296 | ACCCTCCCACCTGGT[A/C]CTCCTCCCACCTTTT | 54793 |
| rs778678624 | in-del | -/GGCAGATAAAATTGGC | 0.0515612 | 0.152059 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444260 | TTTTTTTTTTTTTTT[-/GGCAGATAAAATTGGC]TTTTAAAGTCACTTA | 54793 |
| rs778794171 | snp | G/T | 1.64762e-05 | 0.00287016 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439650 | CTGTCAGGTTCTTTA[G/T]TCACTAAAGTGCTCC | 54793 |
| rs779020484 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440059 | TATCTAAAAAGCATG[-/T]TTTTTTTTTTTTTTT | 54793 |
| rs779054968 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445239 | ATAAAAATCTGTTTT[-/C]ATTAACAAAACCCAA | 54793 |
| rs779157104 | snp | C/T | 3.31016e-05 | 0.00406813 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429823 | TAAGGAAAACATTTT[C/T]ATCTTTTACATCTTC | 54793 |
| rs779248970 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445612 | GTAAGGTGAACTACA[A/C]ACTTGTTTTAAAGAG | 54793 |
| rs779249156 | snp | C/G | 1.65277e-05 | 0.00287464 | intron-variant | KCTD9 | GRCh38.p7 | 8:25429980 | ATCACAATTCTGCAA[C/G]ATGAAAACAATATTC | 54793 |
| rs779282052 | snp | A/G | 1.65523e-05 | 0.00287678 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435407 | GTTCAAGATTTGCAC[A/G]GCAAAGATTTGCATG | 54793 |
| rs779359596 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446540 | TAGACCTACACTTCG[A/C]TCTAGAGTCTGACAT | 54793 |
| rs779490469 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433479 | GTAAGGTTCATAATT[C/T]TGTTCAAATTAGCTC | 54793 |
| rs779512611 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451462 | GTGCTTACAAAGGTC[-/A]ATTTACTTTGTATGT | 54793 |
| rs779628357 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431123 | GGCATGAGCCACTGC[A/G]CCTGGCCCCAAAGTA | 54793 |
| rs779672530 | in-del | -/T | 1.89353e-05 | 0.00307689 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436520 | TCTGAAACAACCTAA[-/T]TTAGTGAATGTATTA | 54793 |
| rs779689274 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430245 | TATTTTATAAGGAGA[C/T]ATTGAAAACAGGGGT | 54793 |
| rs779740063 | snp | A/T | 1.95589e-05 | 0.00312715 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436527 | CAACCTAATTTAGTG[A/T]ATGTATTACATTCAT | 54793 |
| rs779760772 | snp | C/T | 3.29832e-05 | 0.00406085 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436373 | GAGTCTTTTGGGAGA[C/T]AGCTACAATGAATGT | 54793 |
| rs779845346 | snp | C/T | 9.06742e-05 | 0.00673267 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458192 | CGCCCCCTCACGCCC[C/T]CGTTACCTTTCCGTT | 54793 |
| rs779911273 | in-del | -/C | 5.53143e-05 | 0.00525872 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444246 | TGTCATTCCATCTTT[-/C]TTTTTTTTTTTTTGG | 54793 |
| rs779936488 | snp | C/T | 1.65701e-05 | 0.00287833 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430002 | ACAATATTCATGTAA[C/T]TCATGTGGAAATTTC | 54793 |
| rs779939594 | in-del | -/ACACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430811 | CAACATAATAAATAC[-/ACACAC]ACACACACACACACA | 54793 |
| rs780025420 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450082 | GTATTTCCTTGTAGG[A/C]TGTAAAACTACTAAG | 54793 |
| rs780248695 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442086 | CCACCCTACATACAA[C/T]AGAGTCCTGAAAGAA | 54793 |
| rs780306704 | snp | C/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460267 | TCAAAAGACAAGCCC[C/T]CTGAAACCAAGGAGT | 54793 |
| rs780314234 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455753 | CCAATCTGTGAAGAA[A/G]ACACTATTAACCTTT | 54793 |
| rs780514316 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432767 | AATCTTGTCTCTCAA[C/T]GAACTTATATATATA | 54793 |
| rs780538380 | snp | C/T | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440595 | GTAGTTGTAAAGTAC[C/T]GCCCTCCAACATTTA | 54793 |
| rs780592544 | snp | A/G | 1.79544e-05 | 0.00299615 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458275 | CTGGGTCCTGAGTGA[A/G]CCGCCACCCTCCCAC | 54793 |
| rs780690924 | snp | C/T | 2.03444e-05 | 0.00318933 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458199 | TCACGCCCCCGTTAC[C/T]TTTCCGTTCTTGGGG | 54793 |
| rs780932598 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449665 | TGAGTCTATTTAAAT[C/T]TTAATCTATTAAAAT | 54793 |
| rs780986083 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451184 | CAATACTAATATTCA[A/C]ATATGCAAAAACTCT | 54793 |
| rs781086289 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440872 | ATACCAACAGCTATA[A/T]GAGCAGCATGCTTTC | 54793 |
| rs781150717 | in-del | -/ATTTA | 1.79046e-05 | 0.00299199 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435327 | TTCAATAGACTAAAC[-/ATTTA]ATTTTCTCTTGTAGC | 54793 |
| rs781343813 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454360 | AATGAATGAATGAAT[C/G]ATGAATTAATCAGTA | 54793 |
| rs781404701 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443771 | ATCAAATACTTTATC[G/T]TCCTTTCGGCCTTTT | 54793 |
| rs781416370 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441813 | CCTGGGCAACAGGGC[A/T]AAACCCCAAAACCCC | 54793 |
| rs781467473 | snp | A/G | 0.000198863 | 0.00996955 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439238 | AACTTACAAAAATGT[A/G]AGTAGTTACATAATT | 54793 |
| rs781474898 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, splice-acceptor-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460382 | TATGTCGTCCGTTTC[A/G]GGAAATGCCTCTTTC | 54793 |
| rs781547081 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432903 | GATAAGGGAGTGAAG[C/T]AGTCTCCTAAATATA | 54793 |
| rs781557544 | snp | A/T | 1.90532e-05 | 0.00308646 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444284 | AATTGGCTTTTAAAG[A/T]CACTTACCAATAAAT | 54793 |
| rs781562809 | snp | A/T | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460463 | TCCTAATCCTTGCAC[A/T]CCAGATACTTTTAAA | 54793 |
| rs781641755 | snp | C/T | 9.99117e-05 | 0.00706724 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432650 | CACCTACAGTGAACA[C/T]ATTCTGGGAGTAGTT | 54793 |
| rs781705086 | snp | A/G | 3.4503e-05 | 0.00415335 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25433400 | TGCTCCTTCTGCATT[A/G]GAACAGAGCATCTTG | 54793 |
| rs796160398 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442374 | CCAGAATAAAATGCA[A/G]TAACATATTTAAGAT | 54793 |
| rs796267923 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449542 | ATTGTCGTCTACTTC[C/T]ATATGATTGACTTGG | 54793 |
| rs796292849 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448783 | AGCCGGGCGTGGTGG[C/T]GTGTGCCTGTAGTCC | 54793 |
| rs796294126 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433056 | AAGAATATTTTATTC[C/G]ATTTGAAAGTTTAAG | 54793 |
| rs796318654 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452996 | ATATAGGAAGACATT[A/G]TCTCCACAAAAAACT | 54793 |
| rs796397651 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440180 | TCTCCTGCCTCAGCC[C/T]CCCAAGTAGCTGGGA | 54793 |
| rs796597104 | multinucleotide-polymorphism | AG/TA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451726 | GGCTAGTTTTAATTT[AG/TA]CTTTAAACACCATTT | 54793 |
| rs796702122 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442874 | TTTTAGATGTGTTCT[A/G]TATGGGGTAAAGTAA | 54793 |
| rs796769349 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434474 | AACACAAACAAAGAT[G/T]CCTCTCGACATTTCA | 54793 |
| rs796929143 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449569 | TTGGTTTTTCTGTGG[-/G]TCTATTGTCTTCCGA | 54793 |
| rs796950128 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433277 | TTTCCAGGGCTTTTT[-/T]CCTTTACAGTCTGCT | 54793 |
| rs796954019 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450178 | TCAAAAACAATTTAC[C/T]GTATCACTAAATATT | 54793 |
| rs796985017 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453698 | TGCATATATATGTGA[C/T]AAAACTATTTAAAAA | 54793 |