| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs553279023 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706705 | CCGTGGGCTCTGCAG[A/G]GCTGACGTGGTACAG | 54442 |
| rs553325317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699749 | CAGCCTCCCTGGGTC[A/G]CCTGGGCTGGGGCCA | 54442 |
| rs553369891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694239 | CTGGCCCTGTGGCCC[C/T]GGCCCTTGCTTGAGA | 54442 |
| rs553562971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690125 | GATGAGCAGAGCGGC[C/G]AGTCTTGTTACCACA | 54442 |
| rs553565187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684099 | AGCTGTGATTTTCCT[G/T]TTATAAGTGTGGGTG | 54442 |
| rs553648265 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684506 | CGCGGTGGCTCACGT[C/G]TGTAATCCCAGCACT | 54442 |
| rs553718936 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691539 | CAGGCCCGGCGCGCC[A/G]AGTCCACGCAGCCTG | 54442 |
| rs553759443 | snp | A/G | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709080 | GGGGAATGCCACCCC[A/G]GGTCGCTCGGACCAA | 54442 |
| rs553833719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697710 | TCACCACGGCCCCTC[C/T]GCCCATTATCCCAGG | 54442 |
| rs553873809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691028 | GGCACCACGAGTAGC[C/T]CCCGCACACATTAGG | 54442 |
| rs553971191 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681413 | CGCCTCCTGGGTTTA[A/G]GCAATTCTCTGCCTC | 54442 |
| rs554028809 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680832 | AACTGAACGAGCCTA[C/G]GTGTGTACCTGAATT | 54442 |
| rs554085702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705711 | TGGGGTACAGCCTCA[A/G]GGGCCCCCTGGTTGG | 54442 |
| rs554094251 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683044 | AGTCGATTCACCTTG[C/G]GGGTGTCTCTTCCTC | 54442 |
| rs554132096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687219 | CCTGAGAAAAGGACT[C/T]GACTCTGGTGATGAA | 54442 |
| rs554134286 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691754 | GCCTTGGCTCCCAGC[A/G]AGGTTGGCAACAAGC | 54442 |
| rs554362866 | in-del | -/T | 0.00476085 | 0.0485567 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695219 | AGTGCCTCTCAGGGG[-/T]TCCCTCCACCCAGGT | 54442 |
| rs554518904 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708136 | TCACGGGGAGCTGGC[G/T]TCTGTCAGTGCCTTG | 54442 |
| rs554855344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693306 | GGTATCACGTGATGG[C/T]AGCAGCTGCACCAGT | 54442 |
| rs554890299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688123 | CAAATGTGATGCCCC[C/T]GCCCCGTACCTGGTG | 54442 |
| rs555171045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693579 | CTCTGTCCTGCTGTG[C/T]AGTTTCCGCCGATGG | 54442 |
| rs555191745 | snp | C/T | 0.000771903 | 0.0196305 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699243 | CTCCATGCAGGCGGG[C/T]GGCCCTGGTGGCTCA | 54442 |
| rs555265427 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698600 | CTGAGCCCGCCCCCC[A/C]CACCCAAGCTCAGCT | 54442 |
| rs555269238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703203 | ATTTCCTCTAAGCAC[A/G]TTCTTAAGGTTGAGG | 54442 |
| rs555298594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691476 | TGGGTTCTAGGGCCA[C/T]GCAGGGCTCTGCAGT | 54442 |
| rs555409545 | snp | C/T | 1.65795e-05 | 0.00287914 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699815 | CTGTGCCCATTGTCC[C/T]TGCAGGTGCCTGTGA | 54442 |
| rs555446149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700215 | TCTGTGTGAGGGAGG[G/T]GACTGGCGTCCCCAG | 54442 |
| rs555476854 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705144 | CGCCAGAGTGACGAC[A/G]AGGACCAGGGGCACC | 54442 |
| rs555496349 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704082 | GCTCTGTACTGTGAG[A/G]AAGCTCCAGGCATGA | 54442 |
| rs555530218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691045 | CCGCACACATTAGGC[C/T]GATCTGGAACATGTG | 54442 |
| rs555564581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685525 | TAGTGCTAATTCATA[C/T]TAGTCACGTTACTAA | 54442 |
| rs555580430 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695272 | GTCTGTTTTGTAAAC[A/G]TCTCGGCCTCCGTGA | 54442 |
| rs555588025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697624 | CTCCATACCTGGCGG[G/T]TCACTGGAGGTCACT | 54442 |
| rs555665358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703399 | GGAGCCAGCCTGGGG[C/T]GAAGGCTCGGGGCAT | 54442 |
| rs555705725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697194 | GCTGGGTGTTGTCCT[G/T]AGCTGCCATGTGCCA | 54442 |
| rs555720783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696554 | ACGGCGCCCACACGC[A/G]TTGGGCCCAGGCTGG | 54442 |
| rs555733827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692611 | ATACTAATTGGTTCA[C/T]GGGCAGGCCCGGAAA | 54442 |
| rs555757368 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690170 | GCTCTCCTGACCAGA[C/T]GTCCATCTGCGGCTG | 54442 |
| rs555807572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698135 | CCCTTGTCCTCTGTC[A/G]CTGCCCCAGTGCCTG | 54442 |
| rs556004284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687794 | GGTCTTTAAAGCCTG[A/G]GGAAGAACCTGCCTG | 54442 |
| rs556110535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684577 | GAGACCATCCTGGCT[A/G]ACATGATGAAACTCT | 54442 |
| rs556178846 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681322 | TTATTTAAATTCTTT[C/T]TTTTTCTTGAGACGG | 54442 |
| rs556200783 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682127 | CAAATATTTGTGCTT[C/T]AGGTGTAGTTACCAG | 54442 |
| rs556397024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686874 | AGAAGTGGGGATCAC[A/G]TCTAGTGGAGATGGC | 54442 |
| rs556437710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687899 | CCTGGGCGTCAACTC[A/G]GCAGTTCTCCATGGA | 54442 |
| rs556449310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706311 | CTCTCCGGTCAGTGC[A/G]GCATGGCAGTGACCT | 54442 |
| rs556534677 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699342 | AGGTGGATGGAGTTT[C/T]AGGAAGCAGCTCAGC | 54442 |
| rs556547782 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694406 | TCACCCTAAGGAGTA[-/G]GGGGGCCGCCGAGGC | 54442 |
| rs556654602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700672 | GCTTCTGTCTGGGGC[A/G]GGTTCTGTCCATGGC | 54442 |
| rs556768836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706150 | TAGAAGTGGTCCAGG[G/T]CACTGAGCCTGGGGG | 54442 |
| rs556772215 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696623 | GCTCGAGGCCTCGCC[C/G]TGAAGGCTGAGGGTT | 54442 |
| rs556938756 | snp | C/T | 1.66449e-05 | 0.00288482 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707259 | TCAGGGACACCTCCT[C/T]AGCCCAAGTCCTCAT | 54442 |
| rs556983339 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708649 | TCACCTGATTAACCA[A/C/G]TTCTCCAGCATTAGG | 54442 |
| rs557117099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700262 | CACTATCCAGCGCAA[C/T]CCCCGTCCCCCACAG | 54442 |
| rs557149248 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707563 | GGCGCTGCCTCTTGG[A/G]GGGGCCTCGCTCTGT | 54442 |
| rs557156505 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704263 | TGGGGGATTGCGGGG[A/G]CCAGAGCTGGAGGAC | 54442 |
| rs557233467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704809 | GGTCCACAGAGCCCA[C/T]GCAGCAGAGGCCCTC | 54442 |
| rs557265870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688493 | TGACCTCAGGTCATC[C/T]GCCCTCCTTGGCCTC | 54442 |
| rs557267454 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709148 | CGGCGGCTCACTCAG[A/G]GCTCTGCCTCTGCCT | 54442 |
| rs557300891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683151 | GGTTCTTTTGCCCAG[A/G]GTGTGTGAACGCCTT | 54442 |
| rs557301376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703755 | TCCTGCTCCACTGCC[A/G]TTCCTCGAGGCCGAG | 54442 |
| rs557468762 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708053 | CACAGGGCTTGCCGC[A/G]TGGAGACTGATCTGT | 54442 |
| rs557560201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689673 | TCATTCCTCACTGCC[A/G]TTTTCTTTTCTTTTT | 54442 |
| rs557654608 | snp | A/G | 0.000749064 | 0.0193383 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699320 | GCCAGGCAGGTGGGG[A/G]ATTAGGAGGTGGATG | 54442 |
| rs557722651 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690524 | TCTTAATTATGGCTG[G/T]TTTAGAAAAAAACCA | 54442 |
| rs557845914 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701394 | GGCCAGACCGGACCC[A/T]GGGTCCCCAGTGGTC | 54442 |
| rs557851406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690229 | GTCAGCTCTGTCTGC[A/G]GAGTCTTCCTCCGTC | 54442 |
| rs557851550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696931 | TGTCGTGGAGCCGCT[C/T]GAGTCGAGGCTTCGC | 54442 |
| rs557858469 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703996 | GTTTTTTATTTCTGA[A/G]CTGAGTTTTTATAAC | 54442 |
| rs557863686 | snp | C/G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681504 | TTTGGTAGAGACGGA[C/G/T]ATTCACCATCTTGGC | 54442 |
| rs558185441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685384 | GTGGGCTGAGGTTGC[A/G]CCACTGCACTCCAGC | 54442 |
| rs558314118 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708097 | GCGAGGTAGCAGTGT[C/T]GCCTCGCCCCTCCCA | 54442 |
| rs558354120 | in-del | -/C | 0.276013 | 0.248643 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700804 | TAGGGTACTTGGAGC[-/C]CCCCCCCCCCTTAAA | 54442 |
| rs558776487 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693829 | TACACGAGCTGGTCT[-/C]CCCCCACCTTTTGCT | 54442 |
| rs558797850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682987 | CCCTGGGAGGGGAGG[G/T]TGAGGATGGCGCCCT | 54442 |
| rs558974168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706682 | GGGGAGGGCAGGGGG[C/T]CGAGGGGCCGTGGGC | 54442 |
| rs559158653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684647 | GCGAGCACCTGTAGT[A/C]CCAGCTACTAGGCAG | 54442 |
| rs559172611 | snp | C/T | 9.95718e-05 | 0.00705521 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702400 | GAACGAAGACCAAGC[C/T]GAGTTCCTCTGTGTG | 54442 |
| rs559220319 | in-del | -/GGAGGGGATCCCCGCAG | 0.0150606 | 0.0854603 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706725 | ACGTGGTACAGATGA[-/GGAGGGGATCCCCGCAG]CGTGATCTGCACTTG | 54442 |
| rs559223606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699657 | GCAGCTGTTCGGGCC[A/G]CGTGTTTTGCTTTTG | 54442 |
| rs559267942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707085 | GCCATGCACAGTGAG[C/T]GCTCCCTGTGTGGGG | 54442 |
| rs559396897 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696681 | CTGCTCCCCCGGGTC[C/T]GTGTCTGCGCATCGG | 54442 |
| rs559523456 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682912 | CGGGCGACTCTCCTC[C/G]GGCTTCGAGCCCCGC | 54442 |
| rs559564132 | snp | C/T | 0.046775 | 0.145601 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695778 | AGGACGTGGCCACAC[C/T]GTCAGGGGTTTCCTG | 54442 |
| rs559783131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688332 | CTCGGCTCACTGCAA[C/G]CTCTGCCTCCTGGGT | 54442 |
| rs559807141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693440 | TTAATGGAAAAGCCA[A/G]CCCCGCCCAGTGGTA | 54442 |
| rs559819051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688528 | AGTGCTGGGATTACA[A/G]GTGTGAGTGTACTTT | 54442 |
| rs559956440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697366 | GGGAAGAGCTGGAAG[A/T]GACCCTCTCAGCCAG | 54442 |
| rs560025474 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704496 | TGCTTCCCACGCCAG[G/T]CCCTCAAGAACTTGC | 54442 |
| rs560087330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692628 | GGCAGGCCCGGAAAA[C/T]GCACCACAAGTCCCC | 54442 |
| rs560133424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705038 | CGTGGCCTCACTGGA[A/C]GGTCACCGGGCGTGG | 54442 |
| rs560179233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685989 | TTGGGAGAGCACCCT[G/T]CTAAAGCATCCTATC | 54442 |
| rs560217215 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692756 | AATCTATCTGCCTCC[G/T]GCTGCCATACATGGC | 54442 |
| rs560293394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701463 | GGACACAGGGGCTCC[A/G]GGGGGCATGGCCGTG | 54442 |
| rs560369854 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705326 | AGATCCTCAGTAGCA[C/G]TGTCTTGGTGGTGGG | 54442 |
| rs560455429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701036 | GGTGGGGCTGGGGCC[C/T]TGGGAAGCCGTGTCA | 54442 |
| rs560468827 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681021 | TTACGACTGTTAAGT[C/T]GGATGTTGGCAAAAT | 54442 |
| rs560663188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682854 | TCCCGGCCTGCGGCT[C/T]CTGCACACGCCCTGC | 54442 |
| rs560714434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697102 | CTGTGCGGGACCCAT[A/G]CGGGGCCGGGAAGCC | 54442 |
| rs560738702 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690480 | TGAGACGCGGGGAAG[A/G]TGAGGGAAATGACTT | 54442 |
| rs560800270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703455 | ATGAGAGGCCAGAAC[C/T]GGAAGGCTTTTAACT | 54442 |
| rs560874084 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687501 | GGAGTCAGAAAGCTG[G/T]TCCACCTGCCTGTTT | 54442 |
| rs560892318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699096 | CCTGGCATGAGTCAC[C/T]ACCTTAAGGTCAGGG | 54442 |
| rs560899244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693471 | GGAGTGGCCAAGACA[C/T]GGCAGCGGCCTACCC | 54442 |
| rs560953058 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707713 | TCACTGGCAGGAAGC[A/G]GCCGCAGCCGCGTCA | 54442 |
| rs561102039 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698265 | GTTGGGCACGGGAGA[C/T]GTGTGTAGGGAAGGA | 54442 |
| rs561133345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687712 | GGACTCCTTTTCAGA[C/G]ACTTGTAGGCACTTT | 54442 |
| rs561135192 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681747 | ATTACAAAAACTTTC[C/T]TTTTTTTTTTTTGAG | 54442 |
| rs561172044 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682363 | TGCCCAGATCACCCC[C/G]TGCTCCGCTCCCGCC | 54442 |
| rs561321570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706699 | GAGGGGCCGTGGGCT[C/T]TGCAGGGCTGACGTG | 54442 |
| rs561409300 | snp | A/G/T | 4.99121e-05 | 0.0049954 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702442 | GCTGCACAACACCCC[A/G/T]TACGGTACGGCCAGC | 54442 |
| rs561648570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696712 | TCTGCACTGGGCAGC[A/G]TCTGACTCCGTTTCT | 54442 |
| rs561775191 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696706 | CATCGGTCTGCACTG[A/G]GCAGCGTCTGACTCC | 54442 |
| rs561805149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700407 | GCTGCGGCGGGTGGG[A/G]TCTGATGGGTCTGTG | 54442 |
| rs561840340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690688 | ATCCCAGTCGTAGAG[G/T]CGTGAGCGGGCCGGG | 54442 |
| rs561923629 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689904 | TGGTGTTGAACTCCT[C/G]ACCTCAGGTAATCCG | 54442 |
| rs561985137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690334 | TGGTTTGGCAACTGT[C/G]CTGCCCGGCCTACGT | 54442 |
| rs562000720 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690724 | TTTCCTTCCTCGTGT[C/G]ATGGGGGCTTGGGCA | 54442 |
| rs562007923 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688360 | GGTTCAAGCATTTCT[A/C]CTGCCCCACCCTCCC | 54442 |
| rs562052877 | in-del | -/TAGAAA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699597 | TTTTATTTTGGAACT[-/TAGAAA]TAGAAATATTTTTGG | 54442 |
| rs562093216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684187 | GCCTTTCTACTCAAG[C/G]ATTCCTGTTTTGTAT | 54442 |
| rs562213050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688710 | CGCCCTGCCAGTCCC[C/T]CTGCTGCCACCCAGA | 54442 |
| rs562321939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704589 | AACAGAGAGAGACAG[C/G]CTCAGATCAGCAAGG | 54442 |
| rs562410026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691558 | CCACGCAGCCTGGGT[A/G]GGTCCTGCATGGGCC | 54442 |
| rs562448944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686966 | AGTGGGTGTCTGCGA[C/T]GCTGATGGACTTTGT | 54442 |
| rs562495540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687242 | GTGATGAAATGGAAC[A/G]TTTCTGATGGGTTCA | 54442 |
| rs562687136 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706869 | GCTTGGGTGAGGGGC[A/G]TCTCCAGGAGGGTCC | 54442 |
| rs562755526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705765 | GGAAGATGGCCTAGG[A/G]AGACAGTGTGTCCAG | 54442 |
| rs562883640 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702072 | CGTCTGTGCTCCGTC[C/T]CCCTGGGGCAGCAGC | 54442 |
| rs562885697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697483 | CACCCCACCCAGTGG[C/T]GTGGCCATGAGCAGG | 54442 |
| rs563045968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705383 | GGGCAGTGTTGGGGC[A/G]TTTGTTGGGATGACT | 54442 |
| rs563076203 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691317 | GGGCCTGTTTCTCGA[A/G]GAAACCCACCAGTTA | 54442 |
| rs563137982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695483 | CGGTTCCTGCATGTA[A/G]GCTGCGGAGGACCCG | 54442 |
| rs563177430 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690230 | TCAGCTCTGTCTGCG[G/T]AGTCTTCCTCCGTCT | 54442 |
| rs563198479 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707757 | CGTGGCCTCTGGTCC[C/G]ACCACCAGGCCCTAG | 54442 |
| rs563249536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693805 | CCTGGCACTCATGGC[A/G]GCCCCGAGCTACACG | 54442 |
| rs563281480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703945 | TCCTCTTGGAGCAAT[C/T]GTAGGGCTCTTTTCT | 54442 |
| rs563289010 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703514 | AACCGCAGACTCTTG[C/G]CTGGGGGCCTCTGGC | 54442 |
| rs563334686 | snp | A/T | 0.110872 | 0.20771 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688759 | AGCACAGGCCCCCGC[A/T]GAGTGGGTCTCCACC | 54442 |
| rs563399154 | snp | C/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707766 | TGGTCCGACCACCAG[C/G]CCCTAGTCTCGGTCA | 54442 |
| rs563487893 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705129 | CTGCGCGCTGCACGC[C/T]GCCAGAGTGACGACG | 54442 |
| rs563571887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699573 | TTGGGATTTCAGGAA[C/T]ATGACTCATTTTATT | 54442 |
| rs563668394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692804 | ACTTTGCTCCAAGAT[C/T]GGAGCAGGCACCAAC | 54442 |
| rs563686868 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700222 | GAGGGAGGGGACTGG[C/T]GTCCCCAGAGCCTCC | 54442 |
| rs563781242 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698627 | AGCTCCCTTGAGAAG[A/G]CACCAGGAGTGGGGT | 54442 |
| rs563846595 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682459 | GGCGCTCTACCAGGG[C/T]GGACCTGTGGGCGGG | 54442 |
| rs563883538 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704834 | GCCCTCCTATCAGGC[C/T]GAGATCTGTGGGCTA | 54442 |
| rs563900172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682889 | TGCGGAGGAGACTTC[A/T]GCGGGAGCGGGCGAC | 54442 |
| rs564001135 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700977 | CCTCCCACGGGAACA[A/G]AAATCTTTGCTGCTG | 54442 |
| rs564014097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688200 | CATGTTTGTACTTGG[C/T]TTTTATTATTAAATA | 54442 |
| rs564066196 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690728 | CTTCCTCGTGTCATG[A/G]GGGCTTGGGCAGGCG | 54442 |
| rs564142357 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685119 | AGATACAGTCGTCTC[G/T]GTCTCATACAATAAT | 54442 |
| rs564160032 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709088 | CCACCCCGGGTCGCT[C/T]GGACCAAGGTGCTGC | 54442 |
| rs564177177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697077 | ACGCCCTGGGTGCTA[C/G]AGAAGGGGGCTGTGC | 54442 |
| rs564244977 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685675 | TGAGGAATCTGAGGA[G/T]GGGGGGAAGGGGTGT | 54442 |
| rs564281737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684590 | CTAACATGATGAAAC[C/T]CTGTCTCTACTAAAA | 54442 |
| rs564508840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705281 | CCTGCCTGTAGTTGA[C/T]GAGAGCCGTCCGCAC | 54442 |
| rs564544772 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700184 | GCGCTGCGCTTTCTT[C/T]GCATCATCTGGCACC | 54442 |
| rs564559421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706948 | GGAGAGACTTAATTG[A/G]GGAGGGGGGACTGGA | 54442 |
| rs564623730 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684285 | TGGAGCACTTGATTC[C/G]CAGTTGATGAACTTT | 54442 |
| rs564684056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700487 | ATGGGCCACTGTGCC[A/G]TGGCATTGTGGCTTG | 54442 |
| rs564721433 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703395 | GTGGGGAGCCAGCCT[A/G]GGGCGAAGGCTCGGG | 54442 |
| rs564844370 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704970 | GCCTCACACGTGGAG[G/T]TTTCCACCTCTGAGA | 54442 |
| rs564853043 | snp | A/G | 0.00636936 | 0.0560724 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681687 | TTGATATACAGCCTT[A/G]AATGTGAATAATTAC | 54442 |
| rs564858100 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682242 | GACCAGTTCATGAAC[C/T]GGAGTCAGGGTGGGG | 54442 |
| rs565080162 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702959 | CAGCCACTACGTGGG[C/G]CTCATCTTTGTCGAG | 54442 |
| rs565108271 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687274 | TCCTACCTAGGAAGA[A/G]TGAAAGAAAACAGTT | 54442 |
| rs565117116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702148 | ACAGAGGAAGAGCTC[G/T]CCCCATGCCATGCCA | 54442 |
| rs565174568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687269 | TTCAGTCCTACCTAG[A/G]AAGAATGAAAGAAAA | 54442 |
| rs565312922 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688428 | GCTGATTTTTGTATA[G/T]TCAGTAGAGAAGGGG | 54442 |
| rs565338440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705831 | AGCCCGTGCTGCTCC[C/T]GGCCTTGGGAGGGCG | 54442 |
| rs565412993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697786 | GCCTGAGCAGCTCCC[A/G]CTGGGCCGAGCCATG | 54442 |
| rs565423504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701709 | CTGCTGCTGTCATGC[G/T]TATTGTGATTTGCGT | 54442 |
| rs565517533 | snp | A/C | 0.107341 | 0.205301 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693834 | CGAGCTGGTCTCCCC[A/C]ACCTTTTGCTCGTAA | 54442 |
| rs565541302 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708506 | TTGCTTCCGGAACTC[C/T]GGCTTCCCAAGGGGT | 54442 |
| rs565584153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698195 | GTCCCTTGAAGGATC[C/T]ATTCATCCTGCCCGG | 54442 |
| rs565602678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689559 | GAGAGCCGCAGGGCC[A/G]ACCCTCTTTGCAGAG | 54442 |
| rs565602754 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683034 | GAGGATCCTGAGTCG[A/C]TTCACCTTGGGGGTG | 54442 |
| rs565614465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704736 | GCCCCCGTGGCTGAT[C/T]CCTCCTGTGACCCAG | 54442 |
| rs565638887 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683811 | ACATTTGCCATGCAG[A/G]AGGCTTCCCAGAAAG | 54442 |
| rs565808567 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693540 | GCTCAGTGCCCTGCC[A/G]GCTCCTTGGACCTGT | 54442 |
| rs565820445 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703610 | TGGGAACAGAGGGGT[A/G]GGGCCGCCAAGCATG | 54442 |
| rs566005187 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705468 | GCCCCTCCTGGGGGC[G/T]GGGCAGGGAGTGCCA | 54442 |
| rs566155819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698938 | TACCTACCTGTATGA[C/T]GCAGGTGGGCAGGAA | 54442 |
| rs566189635 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687819 | TGCCTGCCTGGCGCC[A/G]TGGGAGGGGTCCTTG | 54442 |
| rs566215062 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706160 | CAGGGCACTGAGCCT[-/G]GGGGGGCACCCGCCT | 54442 |
| rs566293264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703593 | CTTTGGAGGTATGCC[C/T]TTGGGAACAGAGGGG | 54442 |
| rs566403819 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707892 | GCGCCATTCCGAGGC[C/T]GGGCCTTCTTCTGAC | 54442 |
| rs566432154 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703641 | TCTCTCGGAGGCCTG[C/T]GGCCAGCTCACGGCA | 54442 |
| rs566572786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685207 | GAGGCGCGTGAATCA[C/T]CTGAGGTCAGGAGTT | 54442 |
| rs566615982 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704258 | GGCCGTGGGGGATTG[C/T]GGGGGCCAGAGCTGG | 54442 |
| rs566618372 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709106 | ACCAAGGTGCTGCCC[C/T]TCCAAGCCGCCCAGC | 54442 |
| rs566670740 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685353 | GAACCACTTGAACCG[A/G]GAGGCAGAGGTTACA | 54442 |
| rs566686553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701741 | TTGCCTTTTAATTTT[C/T]CCTTTAAAAGCACAG | 54442 |
| rs566710432 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687633 | CGCCAGGGCTGTGGC[C/T]GTGATGGGGGCGCCT | 54442 |
| rs566760718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705550 | GCTCAGGGCCAAGGG[G/T]TCAGGACCAGTGCGG | 54442 |
| rs566778820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700574 | ACGACCTGGCTGCCA[C/G]TGTTCCTGGTGCTAG | 54442 |
| rs566799375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705919 | GCTGTTGGGGCTCCC[A/G]GATGCTCAGATGCCA | 54442 |
| rs566799388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701261 | CCCCTTCCTTGATTA[C/T]GACCTGCTTGGCACG | 54442 |
| rs566939855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698406 | TCGTGTGGGTCTGCG[C/G]AGGCGCCAGAAGGAC | 54442 |
| rs567046419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690436 | TGCCAGCTTGGGCCC[A/G]GCCACAAGTAGGTCA | 54442 |
| rs567049573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702578 | TCTCATCAAGCTCCC[A/G]GTGTCCGCCCCTGGT | 54442 |
| rs567210384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690128 | GAGCAGAGCGGCCAG[C/T]CTTGTTACCACACTT | 54442 |
| rs567273482 | snp | G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681582 | CCCAAAGTGTTGGGA[G/T]TACAGACATGAGCCA | 54442 |
| rs567458032 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709115 | CTGCCCCTCCAAGCC[A/G]CCCAGCCCCACTGGC | 54442 |
| rs567584746 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680838 | ACGAGCCTACGTGTG[C/T]ACCTGAATTTTCCCC | 54442 |
| rs567595083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693015 | GGGCGAACCCCAGGG[C/T]TGCAGCCCCAGGCAG | 54442 |
| rs567608579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697586 | TCGGCGTAGACATAC[A/G]CTGAGCTGCATGTAA | 54442 |
| rs567623179 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681318 | CCTGTTATTTAAATT[C/T]TTTTTTTTTCTTGAG | 54442 |
| rs567626618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691668 | CTGGAGGCACTGGGG[C/T]GGCGGGGGTGTGGAG | 54442 |
| rs567697235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691452 | GCCTCTGGTGCCCGG[C/T]GGCTCAGCTGGGTTC | 54442 |
| rs567699137 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683980 | TCCTGTGCCTCCCCA[C/T]AACTTCCAACTGTTT | 54442 |
| rs567761173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706419 | GACAGCTGTTGTGGG[C/T]CACGCACAGTGAGGC | 54442 |
| rs568100764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693973 | CAGAGGCGAGCCTCC[A/G]CCCTATCTGATCTTT | 54442 |
| rs568189849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689663 | GTCTCCACCCTCATT[C/T]CTCACTGCCGTTTTC | 54442 |
| rs568202895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696205 | CTGGTGCTGAGGCCA[C/T]GGGCAGCGGCGCAGC | 54442 |
| rs568378093 | snp | A/C | 0.00398564 | 0.0444627 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709125 | AAGCCGCCCAGCCCC[A/C]CTGGCCGCGGCGGCT | 54442 |
| rs568495792 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707538 | GTTGGGGGAGCACGG[C/T]GGCCGGGTGGGCGCT | 54442 |
| rs568527008 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698523 | TTGTTGGTGGGCTCT[C/G]CCCAGTACCTCCTGT | 54442 |
| rs568614062 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705681 | GGCCTGCCTGCCTGT[-/G]GGGGTGTCTGGCCAT | 54442 |
| rs568625855 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691667 | CCTGGAGGCACTGGG[G/T]CGGCGGGGGTGTGGA | 54442 |
| rs568685300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699676 | GTTTTGCTTTTGTGG[A/C]TGTGCTCAGGATTGC | 54442 |
| rs568783877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705972 | GCGCTACTTAGTTTT[A/G]CACAGGGCTGGTGGG | 54442 |
| rs568797120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704075 | AGGACACGCTCTGTA[C/T]TGTGAGGAAGCTCCA | 54442 |
| rs568813570 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688381 | CCACCCTCCCAAGTA[A/G]CTGGGATTACAGGCA | 54442 |
| rs568817563 | snp | A/G | 0.000387222 | 0.013909 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699244 | TCCATGCAGGCGGGC[A/G]GCCCTGGTGGCTCAC | 54442 |
| rs568894639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696904 | TCTGGTCGCTTGGGC[A/G]GCCGCTTGTGTTGTC | 54442 |
| rs568971704 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700225 | GGAGGGGACTGGCGT[C/T]CCCAGAGCCTCCTGG | 54442 |
| rs568979531 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680591 | CCCAGTTATTTTCAA[A/C]CTTGACATGAGCCTA | 54442 |
| rs569017992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701802 | TGGGCCAGATGCCTG[A/G]CCAGAGAGACAGGTT | 54442 |
| rs569148316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699989 | ATGGCTCAGGGCTCA[A/G]TGCTCCTGGAAATGC | 54442 |
| rs569179762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697120 | GGGCCGGGAAGCCTG[C/T]GTCTCTGAGGCCCTC | 54442 |
| rs569182248 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702203 | CTCGTGCAGGTGTTC[C/T]GGGGATTTGTTTTCC | 54442 |
| rs569291496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693082 | GACATCTTCAGTGGG[A/G]TGGGTGTGATGGCTG | 54442 |
| rs569320784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688129 | TGATGCCCCCGCCCC[A/G]TACCTGGTGCCAGGT | 54442 |
| rs569456646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698905 | GACCGGGCTGTGTGG[A/G]CACTCCCTGCCTCAG | 54442 |
| rs569504809 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690476 | TCAGTGAGACGCGGG[C/G]AAGATGAGGGAAATG | 54442 |
| rs569690348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703088 | CAGGCCCTTCTGTTT[C/T]CTGCGGGGCAGGCAG | 54442 |
| rs569828762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682978 | GATCCCCTACCCTGG[A/G]AGGGGAGGGTGAGGA | 54442 |
| rs569942197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688386 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCACGAGC | 54442 |
| rs569945349 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681335 | TTTTTTTTCTTGAGA[A/C]GGAGTCTCACTCTGT | 54442 |
| rs570004503 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701009 | GCGAGCCCCACCTCC[C/T]AGTTGTCCCTTGGTG | 54442 |
| rs570064588 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681927 | TGTATTTTCAGTGGA[C/G]ACCGGGCCTCACCAT | 54442 |
| rs570134788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691685 | GCGGGGGTGTGGAGC[A/G]GCTGGCAGGTTCTTG | 54442 |
| rs570172337 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692291 | CGTCCAGGAAGAATG[A/C]GGTAGCAGACAAGTG | 54442 |
| rs570287023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707011 | CATGTCTGAGGCCCA[A/G]GACTGAGTGGGCTGA | 54442 |
| rs570536577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690113 | GGAGTCTGGTGAGAT[A/G]AGCAGAGCGGCCAGT | 54442 |
| rs570608964 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708076 | TGATCTGTTCCATCC[A/G]TTAGCGCGAGGTAGC | 54442 |
| rs570636853 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704824 | CGCAGCAGAGGCCCT[-/C]CTATCAGGCCGAGAT | 54442 |
| rs570757721 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705112 | GCCTGTCTTCTCCCC[A/C]ACTGCGCGCTGCACG | 54442 |
| rs570844635 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704153 | TTTTCCAAAAATACC[C/T]GCTCTGAAGTGGGGC | 54442 |
| rs571000564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706080 | GGACGTGCTGCCCCT[C/T]GCACAGGGGGATGGG | 54442 |
| rs571013365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704620 | GCGGGCACCTGGGCA[A/G]AGGCCGGGGTCTCCC | 54442 |
| rs571039792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706351 | TGTGCCCGGCGAGGG[C/T]GTGGGCGTTGCTGCC | 54442 |
| rs571044933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696447 | CTCCCTCAAGGACAG[C/T]CCAAGGGTGGTGAAT | 54442 |
| rs571083653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699715 | TCGTGCCCTGTGCTG[A/G]GAACTGCAGAGTGGA | 54442 |
| rs571170793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702242 | CCTGAAGCGTCGGCA[C/G]TCTTTGCTGTGGCTT | 54442 |
| rs571210286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694042 | GCCGTGAATAATTCC[C/T]GAGCTGAGCGGTGTG | 54442 |
| rs571292383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691011 | CTGTCTGGGCCTGGG[C/T]TGGCACCACGAGTAG | 54442 |
| rs571372727 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708018 | GATAGACTCCCCAGC[A/G]TTTTTCCTCTGGAAA | 54442 |
| rs571403909 | snp | C/T | 0.000133462 | 0.00816782 | missense | KCTD5 | GRCh38.p7 | 16:2697993 | GAGACAGCAAAACAT[C/T]GCAGGTGAGACAAAT | 54442 |
| rs571478279 | snp | C/G | 1.71666e-05 | 0.00292968 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702529 | TGGGTGGGGAAGGCT[C/G]TTGCCCTCTCAGACC | 54442 |
| rs571505023 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708464 | CAGAGTCTGGGGACT[C/T]GGCGTGCAGGGCGGG | 54442 |
| rs571523963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706236 | AGCAGCTCAGGGGAC[A/G]TGGCCTCCAGGAGCC | 54442 |
| rs571583274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691354 | ACCCATGGGAAGAAA[C/T]GGCCGGAGAGCTGTG | 54442 |
| rs571601696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697534 | CCTCCAGGCTTGGAG[A/G]GAAAATGCCAGATCC | 54442 |
| rs571609116 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701129 | TTGTGACTTCTGGCT[G/T]GGAGGGAACAATGTC | 54442 |
| rs571685580 | snp | A/G/T | 3.45407e-05 | 0.00415564 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682820 | GGGCCTCACGGGCCA[A/G/T]CCCGGAGGGTCCTGG | 54442 |
| rs571698888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697140 | CTGAGGCCCTCGTCT[C/T]CTTGTCTCTATCCTG | 54442 |
| rs571761714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687661 | CCTGCTGCCTGGTCT[C/T]GCCCCGGCCCTGTCG | 54442 |
| rs571828416 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699653 | AACAGCAGCTGTTCG[A/G]GCCGCGTGTTTTGCT | 54442 |
| rs571845618 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681207 | AAATTAAAAGAACTC[A/C]TGAAAACAAATAATA | 54442 |
| rs571849017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688089 | CTTACTTTACTGTGA[C/T]GTCCTCTCCTGAAGA | 54442 |
| rs571873563 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708117 | CGCCCCTCCCACTGC[A/G]GGCTCACGGGGAGCT | 54442 |
| rs571884638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685405 | GCACTCCAGCATGGG[C/T]GACAGATCGAGACTC | 54442 |
| rs571910805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703817 | GACAGCCGGGGTGGA[A/G]GCTGGGGTTCCACCG | 54442 |
| rs571984289 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707651 | TGAAGATCGTGTGAA[A/G]GAAGCGTTCTTGGTG | 54442 |
| rs572084994 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682316 | CTCGTGGGAGGTCGA[A/G]GCTGATGTCCGCTGC | 54442 |
| rs572375669 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701534 | GGCACCCCTGTGGCC[A/G]CCTCACTGGGCTGGG | 54442 |
| rs572614714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692654 | TCCCCACTTTGGTCC[C/G]CGGGACTGGCAGCCC | 54442 |
| rs572637378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698209 | CCATTCATCCTGCCC[A/G]GCCCAGACTCTGGGA | 54442 |
| rs572842222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704884 | GGGCCAGAGGCCAGG[C/T]GCCTCTGGACAGGGT | 54442 |
| rs572879005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705130 | TGCGCGCTGCACGCC[A/G]CCAGAGTGACGACGA | 54442 |
| rs572971098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690677 | CGCCTCTCCTCATCC[C/G]AGTCGTAGAGGCGTG | 54442 |
| rs572996320 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681007 | GGTAAAAGCCTCTAT[C/T]ACGACTGTTAAGTTG | 54442 |
| rs573085767 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697003 | GCGCTAGACACAGAC[C/G]AAGGCCCTGCCGCCC | 54442 |
| rs573163330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700810 | TACTTGGAGCCCCCC[C/G]CCCCTTAAAATGTCA | 54442 |
| rs573281046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699476 | AGAGCCTTTCCCGAC[C/T]GATGAATTCAGGGCT | 54442 |
| rs573291635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688595 | TCCCGCAGCCACACT[C/T]AATTTCTGTTAATGT | 54442 |
| rs573422389 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709036 | TATTTATGAATGCGC[A/G]TAGTAGCTGTTTATG | 54442 |
| rs573452242 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684520 | TCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 54442 |
| rs573644693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697711 | CACCACGGCCCCTCC[A/G]CCCATTATCCCAGGA | 54442 |
| rs573683361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691541 | GGCCCGGCGCGCCGA[A/G]TCCACGCAGCCTGGG | 54442 |
| rs573766482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706715 | TGCAGGGCTGACGTG[A/G]TACAGATGAGGAGGG | 54442 |
| rs573860942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706122 | CACTGGAGAGTGAGT[A/G]GGAGCCTCGAGCTAG | 54442 |
| rs573898136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702039 | CTGCCCCCCTCCCTC[C/G]GCCCCAGCTCAGGGA | 54442 |
| rs573993326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705712 | GGGGTACAGCCTCAA[A/G]GGCCCCCTGGTTGGT | 54442 |
| rs574026618 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681439 | GCCTCAGCCTCCGAG[G/T]AGCTGGGATTACGAG | 54442 |
| rs574034070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691032 | CCACGAGTAGCCCCC[A/G]CACACATTAGGCCGA | 54442 |
| rs574165739 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688476 | GGCTGGTCTCGAACT[C/G]CTGACCTCAGGTCAT | 54442 |
| rs574174687 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697043 | GGTCTGCCTCTATCC[A/C]GCCCCGATGCAGCCA | 54442 |
| rs574181688 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704857 | GTGGGCTAGCGCCGC[C/G]TGCCAGGAGTGGGGC | 54442 |
| rs574265137 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692546 | TCTTTGTCCTCTGCC[C/G]TGCTCTGGCTGAGCC | 54442 |
| rs574315985 | snp | A/G | 4.96915e-05 | 0.0049843 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699874 | GGAGGAGGAGCTCAC[A/G]CAGATGGTGTCCACC | 54442 |
| rs574404755 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688485 | CGAACTCCTGACCTC[A/C]GGTCATCCGCCCTCC | 54442 |
| rs574674325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703882 | GATCTAGGAGGCGAC[C/T]CCTGGCTCCCTGAGA | 54442 |
| rs574872997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707209 | CCGAGCTAACCCCAG[C/G]CCTGTGGGCTCTGTT | 54442 |
| rs574992374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692782 | ATGGCGCCTGGGCTC[A/G]GCCCCAACTTTGCTC | 54442 |
| rs575022146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702706 | AGCTGCTCCTGGAAG[C/G]GGCCCCAGGCCTGCT | 54442 |
| rs575122407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693318 | TGGCAGCAGCTGCAC[A/C]AGTTGGCCTGCTGCT | 54442 |
| rs575145562 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698975 | CAGGTGGGAGAGTCT[A/G]CGGTCCAGCCTTGCT | 54442 |
| rs575164359 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686963 | GTTAGTGGGTGTCTG[C/T]GACGCTGATGGACTT | 54442 |
| rs575244447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705184 | GCTCAGATTAAGTGT[A/G]AATGTCATGGTGAGC | 54442 |
| rs575274950 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690248 | TCTTCCTCCGTCTGC[C/T]AGGGCTGTGTGTGCC | 54442 |
| rs575291122 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695385 | GGCCTCCCTCGCTGC[C/T]GGCTCCCGGCCTGTT | 54442 |
| rs575328835 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685592 | TGTAAAATGCTTCAT[C/G]TTAGTTTTGTCTCCA | 54442 |
| rs575336088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701373 | CCCTGCGGGGTGCTG[G/T]GAGGTGGCCAGACCG | 54442 |
| rs575533262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690181 | CAGACGTCCATCTGC[A/G]GCTGCCCTGTGGACC | 54442 |
| rs575567272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697195 | CTGGGTGTTGTCCTG[A/T]GCTGCCATGTGCCAT | 54442 |
| rs575579036 | snp | C/G | 0.106633 | 0.204807 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684191 | TTCTACTCAAGCATT[C/G]CTGTTTTGTATATGA | 54442 |
| rs575693672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698461 | GGCTCGCCACAGACA[C/T]ACCTCTCACAGCTGG | 54442 |
| rs575765195 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709436 | CAGCCTCCTGAGCAG[C/T]TGGGATTACAGGCGT | 54442 |
| rs575976794 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687619 | GAGGTCTAAAGCCTC[G/T]CCAGGGCTGTGGCCG | 54442 |
| rs576103924 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687256 | CGTTTCTGATGGGTT[C/T]AGTCCTACCTAGGAA | 54442 |
| rs576137080 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680891 | AGAAACACCAAACTA[C/T]GTACAGAGAACTTTT | 54442 |
| rs576253982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698155 | CCCAGTGCCTGCCAG[C/T]TCCGTCTACCCGGCT | 54442 |
| rs576259235 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682171 | CTCCTATGCTCCGTA[A/G]TCTTGTAATAAAAAG | 54442 |
| rs576266947 | snp | C/T | 3.63802e-05 | 0.00426483 | missense | KCTD5 | GRCh38.p7 | 16:2682675 | CGCCCTGGCAGCGTG[C/T]CCAAGTGGGTCCGAC | 54442 |
| rs576364064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697768 | GAAGCCTGTTAGGTC[A/G]GGGCCTGAGCAGCTC | 54442 |
| rs576368633 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706157 | GGTCCAGGGCACTGA[C/G]CCTGGGGGGCACCCG | 54442 |
| rs576381272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699508 | CACGGTTGCTGCGTG[C/T]GGAGCAGACGTGGAC | 54442 |
| rs576581309 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706229 | CAGGCTGAGCAGCTC[-/AG]GGGACGTGGCCTCCA | 54442 |
| rs576642475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696655 | CTGGGCACCTGCGTG[C/T]GGGCGTGGCCCTGCT | 54442 |
| rs576659511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702135 | GCTCAGGGTCCTCAC[A/G]GAGGAAGAGCTCGCC | 54442 |
| rs576668429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706554 | GGCCAGCGCCTGAGC[C/G]TGTCCTCAGGGGAGC | 54442 |
| rs576776743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704407 | TTCAGTCAGCGGCGG[C/T]GGGAGAGCCTGGGTG | 54442 |
| rs576835887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684018 | TCATTTGACCAAGCC[C/G]TCTACTCAGAGAATT | 54442 |
| rs576943275 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699270 | CTCACCATCACTCCC[A/C]GGACCACAGCTGCCT | 54442 |
| rs577054084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704851 | AGATCTGTGGGCTAG[C/T]GCCGCCTGCCAGGAG | 54442 |
| rs577092469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700266 | ATCCAGCGCAATCCC[C/T]GTCCCCCACAGCTCA | 54442 |
| rs577264880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703372 | GCCTGGGTGGTGGGG[C/T]GGGCTCTGTGGGGAG | 54442 |
| rs577300463 | snp | A/C/G | 0.00239393 | 0.0345281 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703778 | AGGCCGAGGCAGTGT[A/C/G]GGCTGGGGCAGGCCC | 54442 |
| rs577303075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699022 | TCACTGTCTTGCAGA[A/G]TAAAGCAACTCGGGC | 54442 |
| rs577333044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693390 | GGAGTTCCTTCAAAG[C/G]ATCAGCCACAAAAGC | 54442 |
| rs577573444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693604 | CGATGGCCGTCCCCA[C/G]CCTGCCCTCCTTCCC | 54442 |
| rs577662256 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688498 | TCAGGTCATCCGCCC[A/T]CCTTGGCCTCCCAAA | 54442 |
| rs577676671 | snp | A/C/G | 0.000176029 | 0.00938027 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707492 | GGGTGGTGAGAGACG[A/C/G]GCCCAGCTGTCCAAG | 54442 |
| rs577696398 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701974 | GTCCAGTCAGCTGGT[C/G]CCAGGCTCTTCCCTC | 54442 |
| rs577726144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691195 | TATGGATGTGGAAAT[C/T]TCTCATTGAAAGCTT | 54442 |
| rs577764024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690655 | AGCATCTCACTGGCT[C/T]CCTGGCCGCCTCTCC | 54442 |
| rs577782732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705293 | TGACGAGAGCCGTCC[A/G]CACTCCATGCCAGCT | 54442 |
| rs577888394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687205 | CAGTTCCATAAATTC[C/T]TGAGAAAAGGACTCG | 54442 |
| rs577944197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684868 | GCTTGAACCTGGGAG[A/G]TGGAGCTTGCAGTGA | 54442 |
| rs577988294 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690414 | CCAGCCTGCTGGGCC[C/T]ACTCAATGCCAGCTT | 54442 |
| rs578027369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686908 | TGATGTTCTGTGTAG[C/G]CAGCACTGGTGAGAG | 54442 |
| rs578031302 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701722 | GCTTATTGTGATTTG[C/T]GTATTGCCTTTTAAT | 54442 |
| rs578056826 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703997 | TTTTTTATTTCTGAG[C/T]TGAGTTTTTATAACC | 54442 |
| rs745437145 | snp | A/G | 1.65987e-05 | 0.00288082 | missense | KCTD5 | GRCh38.p7 | 16:2697978 | ACAAAATTAGAGAAC[A/G]AGACAGCAAAACATC | 54442 |
| rs745445569 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690484 | ACGCGGGGAAGATGA[-/G]GGAAATGACTTGTCA | 54442 |
| rs745539779 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688124 | AAATGTGATGCCCCC[A/G]CCCCGTACCTGGTGC | 54442 |
| rs745547850 | snp | G/T | 7.3038e-05 | 0.00604265 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707478 | TTTGCCTCTGAGGTG[G/T]GTGGTGAGAGACGGG | 54442 |
| rs745730581 | snp | C/G | 8.10307e-05 | 0.00636465 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682523 | GCTTCCGGTGGAAGG[C/G]AGCTGTTGCGGGGCT | 54442 |
| rs745747037 | snp | A/C/T | 3.32117e-05 | 0.00407492 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702345 | TCTCAGGCTATGTCT[A/C/T]CTTGCAGTTGGTCAG | 54442 |
| rs745778898 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708281 | CGCCGCTCTCTCATT[C/T]TCTTTGTATAACTAT | 54442 |
| rs745812640 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688174 | GAGGTTGTGCCTGGC[A/G]GTCTTCATTTCATGT | 54442 |
| rs745830428 | snp | C/G/T | 0.000429454 | 0.0146473 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702527 | CTTGGGTGGGGAAGG[C/G/T]TCTTGCCCTCTCAGA | 54442 |
| rs745836551 | snp | C/G | 1.68252e-05 | 0.0029004 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699951 | CTGGTGGCAGCCATG[C/G]TGCAGCTGAACTTGT | 54442 |
| rs746057075 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708519 | TCCGGCTTCCCAAGG[A/G]GTACTGTGCAGACTG | 54442 |
| rs746098413 | snp | C/T | 3.39674e-05 | 0.00412099 | missense | KCTD5 | GRCh38.p7 | 16:2682723 | TACTTCCTCACCACT[C/T]GGCAGACCCTGTGCC | 54442 |
| rs746117684 | in-del | -/TATATTTATT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688242 | AAATATATATATATA[-/TATATTTATT]TATTTATTTATTTAT | 54442 |
| rs746283358 | snp | C/T | 8.17294e-05 | 0.00639203 | missense | KCTD5 | GRCh38.p7 | 16:2682627 | GGCGGCCTGTGCCGC[C/T]GCTGCAGCGCTGGGC | 54442 |
| rs746401868 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704784 | TGCAGCAGTGGGGCC[A/G]ATGCAGTGGGGTCCA | 54442 |
| rs746412300 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704523 | TTGCTAGAAGGACTC[A/G]CAGAGCTCACTGAGA | 54442 |
| rs746541925 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702929 | TCCCTGAGTGCAGGG[C/G]TGGGTACCCTGGCTC | 54442 |
| rs746599561 | snp | A/G | 0.00316425 | 0.0396499 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699212 | ATGTGGGGCCACCCC[A/G]CCCACTGGGGAGCAG | 54442 |
| rs746632459 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704725 | ATCCACCGCCTGCCC[C/T]CGTGGCTGATCCCTC | 54442 |
| rs746734396 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708355 | CCTGCACGGGCTCTG[C/T]CCGACATGCCGTGGG | 54442 |
| rs746850719 | snp | A/G | 6.9052e-05 | 0.00587548 | missense | KCTD5 | GRCh38.p7 | 16:2682565 | TGGCGGAGAATCACT[A/G]CGAGCTCCTGTCGCC | 54442 |
| rs747148611 | snp | C/G | 1.65971e-05 | 0.00288067 | missense | KCTD5 | GRCh38.p7 | 16:2702356 | GTCTCCTTGCAGTTG[C/G]TCAGCATCGGCTCCT | 54442 |
| rs747183843 | snp | G/T | 1.69203e-05 | 0.00290859 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699964 | TGCTGCAGCTGAACT[G/T]GTGCTCACAATGGCT | 54442 |
| rs747212243 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707812 | CTCCCAGGCGGGATC[A/G]CTGGTTTCTCTCGAC | 54442 |
| rs747436311 | snp | A/G | 1.73345e-05 | 0.00294397 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682824 | CTCACGGGCCAGCCC[A/G]GAGGGTCCTGGCCTT | 54442 |
| rs747487962 | snp | G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681979 | CTCCTGACCGCCTGA[G/T]CCTCCCGCCTCGGCC | 54442 |
| rs747526180 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699239 | GCAGCTCCATGCAGG[C/T]GGGCGGCCCTGGTGG | 54442 |
| rs747543049 | snp | C/T | 1.6585e-05 | 0.00287962 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707368 | AATGATTTACGTTTT[C/T]CCGAGATGTAATGAA | 54442 |
| rs747701976 | snp | A/G | 6.60371e-05 | 0.0057458 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707289 | TTTTATGCATTTGGT[A/G]TTTTTCAGATTTTGC | 54442 |
| rs747848357 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704094 | GAGGAAGCTCCAGGC[A/G]TGACCCCAAATCCCT | 54442 |
| rs747861788 | snp | A/C/T | 3.31445e-05 | 0.0040708 | missense | KCTD5 | GRCh38.p7 | 16:2699825 | TGTCCTTGCAGGTGC[A/C/T]TGTGAAGCATGTGTA | 54442 |
| rs748017690 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693003 | ATAGTTTGGGTGGGG[C/T]GAACCCCAGGGCTGC | 54442 |
| rs748040106 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708587 | ACTGTCTGGTTTCCA[A/G]TGCTTCTGGAGACTT | 54442 |
| rs748045320 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691913 | GCTGGCCCCTGAGCA[A/C]AGGGATGGGCTGGAG | 54442 |
| rs748265019 | snp | A/C | 2.06524e-05 | 0.00321337 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682537 | GGAGCTGTTGCGGGG[A/C]TTGCTGGGATCATGG | 54442 |
| rs748324959 | snp | C/T | 0.000449689 | 0.0149881 | missense | KCTD5 | GRCh38.p7 | 16:2702450 | ACACCCCGTACGGTA[C/T]GGCCAGCGAGCCCAG | 54442 |
| rs748331319 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701496 | TGCTCCCAGGGGTAC[A/C]CTTAGCTGCTTGGGC | 54442 |
| rs748376395 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688021 | CTGGCCTGCCTTATG[A/G]CTTGGGGTGATTTCG | 54442 |
| rs748567179 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706346 | GAGGCTGTGCCCGGC[A/G]AGGGCGTGGGCGTTG | 54442 |
| rs748589453 | snp | A/G | 1.65888e-05 | 0.00287996 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697973 | AAAGGACAAAATTAG[A/G]GAACGAGACAGCAAA | 54442 |
| rs748679552 | snp | C/T | 1.75246e-05 | 0.00296007 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682836 | CCCGGAGGGTCCTGG[C/T]CTTCCCGGCCTGCGG | 54442 |
| rs748681271 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698393 | GACAGCAGATGGGTC[A/G]TGTGGGTCTGCGCAG | 54442 |
| rs748715700 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680985 | TACGAATAGGGGTCA[C/T]TGTGCTGGTAAAAGC | 54442 |
| rs748794197 | snp | A/C | 6.1864e-05 | 0.00556131 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707468 | TGAATCCTTTTTTGC[A/C]TCTGAGGTGGGTGGT | 54442 |
| rs748889164 | snp | A/G | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709361 | TCCTTAAGAGACAGG[A/G]GTCTTGCTATGTTGC | 54442 |
| rs748978781 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707878 | GTCACTGCTTCCCGG[C/T]GCCATTCCGAGGCCG | 54442 |
| rs749005743 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681651 | ATTGAATTCATGTTC[A/G]GGGCCACGTTGTTAT | 54442 |
| rs749124755 | snp | A/G | 1.65636e-05 | 0.00287776 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699838 | GCCTGTGAAGCATGT[A/G]TACCGTGTGCTGCAG | 54442 |
| rs749149003 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703908 | TGAGAGCCCCAGCTC[A/G]GTCACAAGGAGGCAC | 54442 |
| rs749176052 | snp | A/G | 3.35655e-05 | 0.00409654 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699944 | GGCCAGCCTGGTGGC[A/G]GCCATGCTGCAGCTG | 54442 |
| rs749193489 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691083 | CCGAGCTGGGAGCAC[C/T]AAGACCCTGCCTACA | 54442 |
| rs749246541 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691896 | TATTTTGCACCCAGG[A/C]TGCTGGCCCCTGAGC | 54442 |
| rs749424609 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693059 | CTCCTCCCGAGGCCC[A/G]GGAACCTGACATCTT | 54442 |
| rs749455936 | snp | A/G | 2.87253e-05 | 0.0037897 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682620 | GCTGGGGGGCGGCCT[A/G]TGCCGCCGCTGCAGC | 54442 |
| rs749492815 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700560 | GGGGGCCCTTGCCCA[C/T]GACCTGGCTGCCACT | 54442 |
| rs749496556 | snp | A/G | 1.66832e-05 | 0.00288814 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707248 | CAGGCGCCTGGTCAG[A/G]GACACCTCCTCAGCC | 54442 |
| rs749601440 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687717 | CCTTTTCAGACACTT[A/G]TAGGCACTTTGGTTC | 54442 |
| rs749645717 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680806 | CATCTGTTGAGATGG[C/T]TGTGGTGAGCAACTG | 54442 |
| rs749710779 | snp | A/G | 1.66891e-05 | 0.00288864 | missense | KCTD5 | GRCh38.p7 | 16:2702456 | CGTACGGTACGGCCA[A/G]CGAGCCCAGCGAGAA | 54442 |
| rs749873679 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697015 | GACCAAGGCCCTGCC[A/G]CCCAGGCTCACCGGT | 54442 |
| rs750011549 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692267 | ACCTTTGTCCAAGTT[C/G]CTGTTCTGCGTCCAG | 54442 |
| rs750034660 | snp | C/T | 8.02729e-05 | 0.00633483 | missense | KCTD5 | GRCh38.p7 | 16:2682585 | CTCCTGTCGCCGGCC[C/T]GGGGCGGCATCGGGG | 54442 |
| rs750068797 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706102 | GGGGATGGGCTCCTC[C/T]GAGGCACTGGAGAGT | 54442 |
| rs750284506 | snp | A/C/T | 4.99084e-05 | 0.00499521 | missense | KCTD5 | GRCh38.p7 | 16:2702441 | AGCTGCACAACACCC[A/C/T]GTACGGTACGGCCAG | 54442 |
| rs750348431 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702014 | AGAGCCGCCCTCCAC[C/T]CTCCTCCCGCTGCCC | 54442 |
| rs750362980 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698845 | CAGGAGCTGCGTCCC[A/G]CGCCCCGGGTCACCT | 54442 |
| rs750374887 | snp | A/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681482 | CATCTGGCTAATTTT[A/T]TGTATTTTTGGTAGA | 54442 |
| rs750426050 | snp | G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682189 | TTGTAATAAAAAGCA[G/T]GTACAGTGTAGACGT | 54442 |
| rs750437707 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692746 | TCTTCCCAGGAATCT[A/G]TCTGCCTCCTGCTGC | 54442 |
| rs750513757 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700648 | TGTCCTGAGTTTCCT[C/G]TGTCACTTGCTTCTG | 54442 |
| rs750522614 | snp | C/T | 1.66868e-05 | 0.00288845 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697894 | AAGACAATTTATTTT[C/T]CCTTATTCCAGGAGT | 54442 |
| rs750676607 | snp | A/T | 3.33784e-05 | 0.0040851 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707445 | TCATTTTTCTAGAGA[A/T]CTGGGTGTGAATCCT | 54442 |
| rs750826775 | snp | C/T | 2.00166e-05 | 0.00316353 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682510 | TTAAAAGCCGGACGC[C/T]TCCGGTGGAAGGGAG | 54442 |
| rs750832512 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707093 | CAGTGAGCGCTCCCT[A/G]TGTGGGGCCTGGAGA | 54442 |
| rs750860551 | snp | C/T | | | splice-donor-variant | KCTD5 | GRCh38.p7 | 16:2709031 | TTGTGTATTTATGAA[C/T]GCGCGTAGTAGCTGT | 54442 |
| rs750924444 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687666 | TGCCTGGTCTCGCCC[C/T]GGCCCTGTCGTTAAC | 54442 |
| rs751023349 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701124 | CCGTCTTGTGACTTC[C/T]GGCTGGGAGGGAACA | 54442 |
| rs751088648 | snp | C/G/T | 3.33579e-05 | 0.00408388 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699925 | CGAGCAGGTGAGGGG[C/G/T]CCTGGCCAGCCTGGT | 54442 |
| rs751178907 | snp | C/T | 1.6599e-05 | 0.00288084 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699799 | GGTGGCCCGCCCTTA[C/T]CTGTGCCCATTGTCC | 54442 |
| rs751207690 | snp | A/G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687643 | GTGGCCGTGATGGGG[A/G/T]CGCCTGCTGCCTGGT | 54442 |
| rs751282891 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705143 | CCGCCAGAGTGACGA[C/T]GAGGACCAGGGGCAC | 54442 |
| rs751284544 | snp | A/G | 0.000102244 | 0.00714924 | missense | KCTD5 | GRCh38.p7 | 16:2682658 | TCGGCGCCCTGGCCC[A/G]GCGCCCTGGCAGCGT | 54442 |
| rs751433290 | snp | A/C/G | 6.07612e-05 | 0.00551159 | missense | KCTD5 | GRCh38.p7 | 16:2682597 | GCCCGGGGCGGCATC[A/C/G]GGGCGGGGCTGGGGG | 54442 |
| rs751528021 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697607 | CTGCATGTAAGCAGC[A/G]GCTCCATACCTGGCG | 54442 |
| rs751572417 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703862 | GCTCTTCCATTTGAG[G/T]CTCGGATCTAGGAGG | 54442 |
| rs751632220 | in-del | -/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703441 | GTTGAGTGGGTGCCA[-/T]GAGAGGCCAGAACCG | 54442 |
| rs751716551 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691694 | TGGAGCGGCTGGCAG[C/G]TTCTTGGTAGACGCA | 54442 |
| rs751768267 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704550 | GAGAGCGCTTAGACT[C/T]AAGGCCGCCATTTAT | 54442 |
| rs751903355 | snp | A/G | 4.97006e-05 | 0.00498476 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697916 | TCCAGGAGTGTTGGA[A/G]GAAGCAGAATTTTAC | 54442 |
| rs752003317 | snp | G/T | 8.43384e-05 | 0.00649323 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707454 | TAGAGATCTGGGTGT[G/T]AATCCTTTTTTGCCT | 54442 |
| rs752313927 | snp | C/T | 1.66258e-05 | 0.00288316 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702333 | CACTGGGCTGCGTCT[C/T]AGGCTATGTCTCCTT | 54442 |
| rs752466163 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698916 | GTGGGCACTCCCTGC[C/T]TCAGTCTACCTACCT | 54442 |
| rs752641327 | snp | C/G | 1.83974e-05 | 0.00303288 | missense | KCTD5 | GRCh38.p7 | 16:2682672 | CAGCGCCCTGGCAGC[C/G]TGTCCAAGTGGGTCC | 54442 |
| rs752700001 | snp | C/T | 3.07602e-05 | 0.00392163 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682614 | GGCGGGGCTGGGGGG[C/T]GGCCTGTGCCGCCGC | 54442 |
| rs752717800 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705684 | CTGCCTGCCTGTGGG[A/G]GTGTCTGGCCATGGG | 54442 |
| rs752803666 | snp | C/T | 1.64814e-05 | 0.00287061 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707332 | CAAGGATGTGAGGGA[C/T]ACAGTATTGACAGCT | 54442 |
| rs752844864 | snp | C/T | | | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702466 | GGCCAGCGAGCCCAG[C/T]GAGAAGGCCAAGGTG | 54442 |
| rs752880583 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705954 | GCTCCTGGCCTGTCC[A/G]CTGCGCTACTTAGTT | 54442 |
| rs752997052 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703569 | CCCCGTGAGCCTCTC[C/T]GAGTAGGCCTTTGGA | 54442 |
| rs753074752 | snp | A/C | 1.66299e-05 | 0.00288352 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699773 | GGGGCCACAGGCAGC[A/C]GTGGGACATGGGTGG | 54442 |
| rs753139295 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692486 | TCAGCAGAGAGGGTA[G/T]CTTCCCTCTGCAGCT | 54442 |
| rs753170198 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708431 | ACAGACCTTTCTCAG[C/T]TGGCTGTGGGGACCT | 54442 |
| rs753373689 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2689832 | AGGCACCCTCCACCA[A/T]GCCTGGCTAATTTGT | 54442 |
| rs753392679 | snp | C/G | 2.01501e-05 | 0.00317406 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682518 | CGGACGCTTCCGGTG[C/G]AAGGGAGCTGTTGCG | 54442 |
| rs753444752 | snp | A/G | 6.65845e-05 | 0.00576956 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682557 | TGGGATCATGGCGGA[A/G]AATCACTGCGAGCTC | 54442 |
| rs753509826 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698343 | GGTAGGGAGCAGAGG[G/T]TGCCAAGGGCCTGCA | 54442 |
| rs753609368 | snp | C/T | 1.66178e-05 | 0.00288247 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702338 | GGCTGCGTCTCAGGC[C/T]ATGTCTCCTTGCAGT | 54442 |
| rs753634572 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700514 | CTTGTCATCGGGGAC[C/T]TCAGGACACGTGAGG | 54442 |
| rs753835706 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704612 | CAGCAAGGGCGGGCA[C/T]CTGGGCAGAGGCCGG | 54442 |
| rs753930507 | snp | C/T | 2.53373e-05 | 0.00355921 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707430 | GAAACCTGCTTTTGA[C/T]CATTTTTCTAGAGAT | 54442 |
| rs753944457 | snp | A/C | 6.87297e-05 | 0.00586175 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682812 | CAAGGTGAGGGCCTC[A/C]CGGGCCAGCCCGGAG | 54442 |
| rs754022505 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708473 | GGGACTCGGCGTGCA[A/G]GGCGGGCTCCAAGCG | 54442 |
| rs754027003 | snp | A/T | 1.64849e-05 | 0.00287092 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707337 | ATGTGAGGGACACAG[A/T]ATTGACAGCTGAAGA | 54442 |
| rs754038203 | snp | C/T | 1.71681e-05 | 0.00292981 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682704 | ACTCAACGTCGGCGG[C/T]ACCTACTTCCTCACC | 54442 |
| rs754132279 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701404 | GACCCAGGGTCCCCA[G/T]TGGTCAGCAGGGGAT | 54442 |
| rs754181729 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706884 | ATCTCCAGGAGGGTC[C/T]GGGCGTCGGGGTGGG | 54442 |
| rs754229928 | snp | A/G | 1.662e-05 | 0.00288266 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699785 | AGCAGTGGGACATGG[A/G]TGGCCCGCCCTTACC | 54442 |
| rs754387786 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690470 | GCCAATTCAGTGAGA[C/T]GCGGGGAAGATGAGG | 54442 |
| rs754517853 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708266 | CAAATGCCTCTCTCT[C/T]GCCGCTCTCTCATTT | 54442 |
| rs754542634 | snp | C/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681658 | TCATGTTCGGGGCCA[C/G]GTTGTTATATGTATT | 54442 |
| rs754666221 | snp | A/C/G | 0.000887388 | 0.0210474 | missense | KCTD5 | GRCh38.p7 | 16:2682559 | GGATCATGGCGGAGA[A/C/G]TCACTGCGAGCTCCT | 54442 |
| rs754725931 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692699 | TGCCCTCCCTGGCCT[A/G]AAGGTGGGGCCTTAC | 54442 |
| rs754831928 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703931 | GGAGGCACTTCTCTT[C/T]CTCTTGGAGCAATCG | 54442 |
| rs754887930 | snp | G/T | 1.68975e-05 | 0.00290662 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702504 | GGCCGGCCCTGGCCT[G/T]GGGCAGTCTTGGGTG | 54442 |
| rs754951656 | snp | A/G | 2.33e-05 | 0.00341313 | missense | KCTD5 | GRCh38.p7 | 16:2682568 | CGGAGAATCACTGCG[A/G]GCTCCTGTCGCCGGC | 54442 |
| rs755043258 | snp | C/T | 3.32834e-05 | 0.00407929 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702445 | GCACAACACCCCGTA[C/T]GGTACGGCCAGCGAG | 54442 |
| rs755166283 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701472 | GGCTCCGGGGGGCAT[A/G]GCCGTGAGTGCTCCC | 54442 |
| rs755192616 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702272 | TTCGCGGTGGCAGGC[A/G]CGTCCTGAGGCTGGT | 54442 |
| rs755210242 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700862 | CGTCCACCCTGGACC[C/G]CTAGGCCGGGGGCCG | 54442 |
| rs755289281 | snp | C/T | 1.65515e-05 | 0.00287671 | missense | KCTD5 | GRCh38.p7 | 16:2697939 | AATTTTACAATATCA[C/T]CTCATTAATAAAACT | 54442 |
| rs755289632 | snp | C/T | 1.66012e-05 | 0.00288103 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702412 | AGCCGAGTTCCTCTG[C/T]GTGGTGTCCAAGGAG | 54442 |
| rs755392417 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687746 | TCTTTTAGCAGCCCC[C/G]CTCCACGCCCCAGGT | 54442 |
| rs755445752 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690592 | GTTGTGTAAGCCGTG[C/G]AACGTATGAGAAAGC | 54442 |
| rs755450816 | snp | A/G | 5.20449e-05 | 0.00510096 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682828 | CGGGCCAGCCCGGAG[A/G]GTCCTGGCCTTCCCG | 54442 |
| rs755522682 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687284 | GAAGAATGAAAGAAA[A/G]CAGTTTTGAGGCTTT | 54442 |
| rs755540160 | snp | C/T | 5.14284e-05 | 0.00507066 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707459 | ATCTGGGTGTGAATC[C/T]TTTTTTGCCTCTGAG | 54442 |
| rs755626988 | snp | C/T | 8.04101e-05 | 0.00634024 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682516 | GCCGGACGCTTCCGG[C/T]GGAAGGGAGCTGTTG | 54442 |
| rs755642011 | snp | C/T | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709240 | TGGATCAGAGCTGCA[C/T]GGCCCATCCCTGCAC | 54442 |
| rs755719010 | snp | A/G | 1.66208e-05 | 0.00288273 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702336 | TGGGCTGCGTCTCAG[A/G]CTATGTCTCCTTGCA | 54442 |
| rs755935393 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698177 | TACCCGGCTCTCCCC[A/T]GGGTCCCTTGAAGGA | 54442 |
| rs756215690 | snp | C/T | 2.91975e-05 | 0.00382072 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682618 | GGGCTGGGGGGCGGC[C/T]TGTGCCGCCGCTGCA | 54442 |
| rs756352948 | snp | C/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680503 | TGCTCACTGCTGAGA[C/G]TTCAGAGATCGCAGC | 54442 |
| rs756534554 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700365 | GGTGCTGCCAGGCCC[A/T]CGTTGCCTTCTCTCT | 54442 |
| rs756587901 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701191 | GCAGCTTCAGGTCTT[C/T]GACCTTAGCACTTCT | 54442 |
| rs756594781 | snp | C/G/T | 3.31908e-05 | 0.00407363 | missense, stop-gained | KCTD5 | GRCh38.p7 | 16:2697977 | GACAAAATTAGAGAA[C/G/T]GAGACAGCAAAACAT | 54442 |
| rs756596252 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687675 | TCGCCCCGGCCCTGT[C/T]GTTAACCACCAGGCA | 54442 |
| rs756641674 | snp | C/T | 0.000926526 | 0.0215036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699150 | TCACTGCTGCGTTTC[C/T]GTCCAGCCCCGTCTG | 54442 |
| rs756854147 | snp | A/G | 4.43616e-05 | 0.00470944 | missense | KCTD5 | GRCh38.p7 | 16:2682558 | GGGATCATGGCGGAG[A/G]ATCACTGCGAGCTCC | 54442 |
| rs756997736 | snp | A/C | 4.98542e-05 | 0.00499245 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702339 | GCTGCGTCTCAGGCT[A/C]TGTCTCCTTGCAGTT | 54442 |
| rs757072298 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705895 | GTCTCCTGCCCTCAT[C/G]AGGAGGGAGCTGTTG | 54442 |
| rs757110584 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697130 | GCCTGTGTCTCTGAG[G/T]CCCTCGTCTCCTTGT | 54442 |
| rs757273707 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681399 | CTAACTGCAACCTCC[A/G]CCTCCTGGGTTTAAG | 54442 |
| rs757319299 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696505 | CTGCTGCTGCCAGCT[-/G]CCGTGTTCCATTCTG | 54442 |
| rs757361468 | snp | C/T | 1.72463e-05 | 0.00293647 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682818 | GAGGGCCTCACGGGC[C/T]AGCCCGGAGGGTCCT | 54442 |
| rs757367095 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704556 | GCTTAGACTCAAGGC[C/T]GCCATTTATTCCCAA | 54442 |
| rs757422164 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692716 | AGGTGGGGCCTTACC[A/G]GGGACCTACCCCCTT | 54442 |
| rs757470471 | snp | A/G | 5.97782e-05 | 0.00546677 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707440 | TTTGATCATTTTTCT[A/G]GAGATCTGGGTGTGA | 54442 |
| rs757478123 | snp | G/T | 1.64855e-05 | 0.00287097 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707339 | GTGAGGGACACAGTA[G/T]TGACAGCTGAAGAAA | 54442 |
| rs757521153 | snp | A/G | 1.70828e-05 | 0.00292252 | missense | KCTD5 | GRCh38.p7 | 16:2682709 | ACGTCGGCGGCACCT[A/G]CTTCCTCACCACTCG | 54442 |
| rs757603907 | snp | C/T | 1.66682e-05 | 0.00288684 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707253 | GCCTGGTCAGGGACA[C/T]CTCCTCAGCCCAAGT | 54442 |
| rs757684757 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708487 | AGGGCGGGCTCCAAG[C/T]GCTTTGCTTCCGGAA | 54442 |
| rs757709684 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701131 | GTGACTTCTGGCTGG[G/T]AGGGAACAATGTCTC | 54442 |
| rs757732853 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700216 | CTGTGTGAGGGAGGG[A/G]ACTGGCGTCCCCAGA | 54442 |
| rs757785831 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687355 | GGTCTTCGGCATTCT[C/T]GCCTCCAGACTTCTG | 54442 |
| rs757805644 | snp | G/T | 8.31428e-05 | 0.00644705 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699181 | CAGCCTGAGTCCTCC[G/T]TAGTGACTGTCCAGG | 54442 |
| rs757950005 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2682883 | GCTTCGTGCGGAGGA[A/G]ACTTCAGCGGGAGCG | 54442 |
| rs757985776 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692322 | GAGGGTGAGCATGAC[A/G]AAGAGAAGCTTTACC | 54442 |
| rs758002962 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687317 | GAGAAGAGCTTGTTT[C/T]GGGGCACCTGACATG | 54442 |
| rs758047911 | snp | C/G | 5.38517e-05 | 0.00518874 | missense | KCTD5 | GRCh38.p7 | 16:2682586 | TCCTGTCGCCGGCCC[C/G]GGGCGGCATCGGGGC | 54442 |
| rs758137944 | snp | A/T | 2.22799e-05 | 0.00333758 | missense | KCTD5 | GRCh38.p7 | 16:2682560 | GATCATGGCGGAGAA[A/T]CACTGCGAGCTCCTG | 54442 |
| rs758250786 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704700 | TTGCGTAGCCATGCT[C/T]GATGGGTGCATCCAC | 54442 |
| rs758303359 | snp | C/G/T | 4.06357e-05 | 0.00450739 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682526 | TCCGGTGGAAGGGAG[C/G/T]TGTTGCGGGGCTTGC | 54442 |
| rs758312408 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705127 | CACTGCGCGCTGCAC[A/G]CCGCCAGAGTGACGA | 54442 |
| rs758358178 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697516 | CCCAGCAGGAAGCGT[C/T]GGCCTCCAGGCTTGG | 54442 |
| rs758503232 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703624 | TGGGGCCGCCAAGCA[G/T]GTCTCTCGGAGGCCT | 54442 |
| rs758506815 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700652 | CTGAGTTTCCTCTGT[C/G]ACTTGCTTCTGTCTG | 54442 |
| rs758560463 | snp | C/T | 1.72922e-05 | 0.00294038 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682821 | GGCCTCACGGGCCAG[C/T]CCGGAGGGTCCTGGC | 54442 |
| rs758594485 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690887 | GATTTTGTGTTTCCC[A/T]TTTTCCCATGTTCCA | 54442 |
| rs758638038 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687126 | GTGCTGGTCCTCAGC[A/C]AACCTGTGCTCACCT | 54442 |
| rs758639166 | snp | C/T | 1.66685e-05 | 0.00288686 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697896 | GACAATTTATTTTTC[C/T]TTATTCCAGGAGTGT | 54442 |
| rs758886697 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708442 | TCAGCTGGCTGTGGG[A/G]ACCTGTCAGAGTCTG | 54442 |
| rs758961782 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707174 | GACCCTGGCCAGTGC[C/T]GCTGGGTTCCCGGGG | 54442 |
| rs759143259 | snp | A/C | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709206 | GCCATCCACGGGGTG[A/C]CGGCTTGGCCAGGGT | 54442 |
| rs759144305 | snp | C/T | 1.70043e-05 | 0.0029158 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682791 | CGATCCCGACCTGGA[C/T]TCAGACAAGGTGAGG | 54442 |
| rs759299918 | snp | C/G | 1.74369e-05 | 0.00295265 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707394 | ATGAACTGCCATGTC[C/G]AGGAAGCTTGGCTGT | 54442 |
| rs759380420 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700877 | CCTAGGCCGGGGGCC[A/G]GGGTGACTCTGGGTC | 54442 |
| rs759428146 | snp | C/T | 3.94929e-05 | 0.00444352 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682662 | CGCCCTGGCCCAGCG[C/T]CCTGGCAGCGTGTCC | 54442 |
| rs759483681 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687600 | CTCTGAAAGGTCACG[G/T]AGTGAGGTCTAAAGC | 54442 |
| rs759518121 | snp | A/G | 0.000164802 | 0.00907599 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707329 | GCTCAAGGATGTGAG[A/G]GACACAGTATTGACA | 54442 |
| rs759590193 | snp | A/G | | | missense | KCTD5 | GRCh38.p7 | 16:2697933 | AAGCAGAATTTTACA[A/G]TATCACCTCATTAAT | 54442 |
| rs759652324 | snp | A/G | 1.65614e-05 | 0.00287757 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699868 | GTGCCAGGAGGAGGA[A/G]CTCACGCAGATGGTG | 54442 |
| rs759694915 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688789 | CTCTGGGGACTGGAC[C/T]CTGCACTGTGGGGAG | 54442 |
| rs759710829 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693475 | TGGCCAAGACACGGC[A/C]GCGGCCTACCCCTGC | 54442 |
| rs759762302 | snp | C/G | 0.00018534 | 0.00962473 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699136 | CTCTGAACCCCTTCT[C/G]ACTGCTGCGTTTCCG | 54442 |
| rs759923599 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704315 | TGGGCTGCGCAGGGC[C/T]GCATGGGCTGTGGGC | 54442 |
| rs759946209 | snp | A/G | 5.06586e-05 | 0.00503257 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682578 | CTGCGAGCTCCTGTC[A/G]CCGGCCCGGGGCGGC | 54442 |
| rs759993139 | snp | A/G | 1.66885e-05 | 0.00288859 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702460 | CGGTACGGCCAGCGA[A/G]CCCAGCGAGAAGGCC | 54442 |
| rs760076323 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691429 | TTCAGCCTACTGCTC[C/G]CCCTTCAGCCTCTGG | 54442 |
| rs760120857 | snp | C/T | 0.000148798 | 0.00862421 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682548 | GGGGCTTGCTGGGAT[C/T]ATGGCGGAGAATCAC | 54442 |
| rs760131405 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692277 | AAGTTCCTGTTCTGC[A/G]TCCAGGAAGAATGAG | 54442 |
| rs760323683 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691217 | TGAAAGCTTCAAAGA[G/T]AGCAGTGGTGAGAGC | 54442 |
| rs760326025 | in-del | -/GTTGTGGGAGTGACAGGCTCAGCCAGTGTCCCTCTGAATGAAAGC | 1.66378e-05 | 0.0028842 | cds-indel | KCTD5 | GRCh38.p7 | 16:2702442 | CTGCACAACACCCCG[lengthTooLong]TACGGTACGGCCAGC | 54442 |
| rs760363989 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701574 | GCCCACTGGGTCAGC[C/T]GCCAGCTATACAGGA | 54442 |
| rs760381362 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708156 | TCAGTGCCTTGTCAC[A/G]CCTGGCATAGAGGTT | 54442 |
| rs760438398 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698864 | CCCGGGTCACCTTGT[C/G]CAGTCTGCTTTTTTC | 54442 |
| rs760623657 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699652 | AAACAGCAGCTGTTC[A/G]GGCCGCGTGTTTTGC | 54442 |
| rs760650577 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682425 | CCGGAACTTCCGCCT[A/G]CCGCGTGACGCCGGG | 54442 |
| rs760677116 | snp | G/T | 3.431e-05 | 0.00414172 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682807 | TCAGACAAGGTGAGG[G/T]CCTCACGGGCCAGCC | 54442 |
| rs760694092 | snp | A/T | 2.458e-05 | 0.00350562 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707425 | GAGAAGAAACCTGCT[A/T]TTGATCATTTTTCTA | 54442 |
| rs760706263 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2686948 | CCTCAGTTTGAGGCC[A/G]TTAGTGGGTGTCTGC | 54442 |
| rs760772787 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697417 | GGGGTCAACTGAGGT[A/G]CCAGGTGACTGAGAC | 54442 |
| rs760802215 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705072 | TTTGGGCCCGGGGCA[C/T]CCGCCCACCCGCACT | 54442 |
| rs761114768 | snp | A/T | 2.38297e-05 | 0.0034517 | missense | KCTD5 | GRCh38.p7 | 16:2682643 | GCTGCAGCGCTGGGC[A/T]CGGCGCCCTGGCCCA | 54442 |
| rs761264552 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703132 | CAGGGACCCCTGCCT[C/T]GTTTGCTTTCAGGTT | 54442 |
| rs761331120 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703060 | CAGCACCGGCGCAGA[C/T]TCTGCGGGGGCTCAG | 54442 |
| rs761386621 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691124 | CGAGTCAGGCCACAG[C/T]GAGACCCGAACCCTG | 54442 |
| rs761434897 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702004 | CCAGGTTTTCAGAGC[C/T]GCCCTCCACTCTCCT | 54442 |
| rs761450252 | snp | A/C | 1.68386e-05 | 0.00290155 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702491 | AAGGTGAGTGCTGGG[A/C]CGGCCCTGGCCTGGG | 54442 |
| rs761466593 | snp | A/G | 3.32579e-05 | 0.00407773 | missense | KCTD5 | GRCh38.p7 | 16:2702437 | AAGGAGCTGCACAAC[A/G]CCCCGTACGGTACGG | 54442 |
| rs761486276 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690293 | TCTGCCATGTGCTCC[C/T]GTGGCCAGGGTCGCC | 54442 |
| rs761562268 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706509 | CTGGAGCTGCCATGG[C/G]TCATTTTGGGAGTTC | 54442 |
| rs761746236 | snp | A/G | 8.87823e-05 | 0.00666208 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707493 | GGTGGTGAGAGACGG[A/G]CCCAGCTGTCCAAGG | 54442 |
| rs761760112 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708084 | TCCATCCGTTAGCGC[A/G]AGGTAGCAGTGTCGC | 54442 |
| rs761844617 | snp | A/T | 3.29478e-05 | 0.00405867 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697865 | TGGATTCTTTGGTTT[A/T]GTTTGGTCTGGTAAA | 54442 |
| rs761972240 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704942 | GACCAGCCCCGGATC[A/G]CAAGATGCAGCCGCC | 54442 |
| rs762025258 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705506 | CGCCAGCCCTAGTGG[C/G]TGACCTTCCTGTCTG | 54442 |
| rs762029230 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693298 | CAGCGGCAGGTATCA[C/T]GTGATGGCAGCAGCT | 54442 |
| rs762226106 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697237 | TCTGGGGTCCTGGAG[A/G]AATGAAGACCACCCA | 54442 |
| rs762366390 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699643 | GGAAGCAGAAAACAG[C/T]AGCTGTTCGGGCCGC | 54442 |
| rs762402856 | snp | A/G | 1.6649e-05 | 0.00288518 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699919 | GAAGTTCGAGCAGGT[A/G]AGGGGCCCTGGCCAG | 54442 |
| rs762493711 | snp | A/G | 1.69175e-05 | 0.00290834 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682767 | CTTCCTGTACCGCTT[A/G]TGCCAGGCCGATCCC | 54442 |
| rs762527099 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701799 | CCATGGGCCAGATGC[C/G]TGGCCAGAGAGACAG | 54442 |
| rs762551065 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701066 | AGCAGCTCGGGGTCC[A/G]CGAACAGGGCTGTCC | 54442 |
| rs762576695 | snp | C/G | 2.17791e-05 | 0.00329986 | missense | KCTD5 | GRCh38.p7 | 16:2682651 | GCTGGGCTCGGCGCC[C/G]TGGCCCAGCGCCCTG | 54442 |
| rs762742114 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691178 | AAGACCCTGGCACTT[-/C]CTATGGATGTGGAAA | 54442 |
| rs762938197 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705726 | AGGGCCCCCTGGTTG[A/G]TGTCTGCAGTTGGAC | 54442 |
| rs762976755 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703257 | ATCCAAGCAGAATCT[A/G]ACCTTGGCCTGGGCC | 54442 |
| rs762982213 | snp | C/T | 0.0001202 | 0.00775147 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699284 | CAGGACCACAGCTGC[C/T]TGGAGGGGCACAGCA | 54442 |
| rs762995573 | snp | A/G | 3.40878e-05 | 0.00412829 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698029 | AGGCTGGAAGCTTGT[A/G]TGGCTGGTGTGAAGG | 54442 |
| rs763431047 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692518 | GTCTTCCACTTGCCA[A/G]TTGTCTCTGTCCTCT | 54442 |
| rs763445930 | snp | G/T | 4.34452e-05 | 0.00466055 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682554 | TGCTGGGATCATGGC[G/T]GAGAATCACTGCGAG | 54442 |
| rs763446749 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708023 | ACTCCCCAGCGTTTT[C/T]CCTCTGGAAATGCCC | 54442 |
| rs763453085 | snp | C/T | 2.08514e-05 | 0.00322881 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682541 | CTGTTGCGGGGCTTG[C/T]TGGGATCATGGCGGA | 54442 |
| rs763536927 | snp | A/T | 2.00246e-05 | 0.00316416 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682511 | TAAAAGCCGGACGCT[A/T]CCGGTGGAAGGGAGC | 54442 |
| rs763544870 | snp | A/C | 1.65905e-05 | 0.0028801 | missense | KCTD5 | GRCh38.p7 | 16:2702369 | TGGTCAGCATCGGCT[A/C]CTCTTACAACTATGG | 54442 |
| rs764001001 | snp | A/G | 8.41404e-05 | 0.00648561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697860 | AAGCGTGGATTCTTT[A/G]GTTTAGTTTGGTCTG | 54442 |
| rs764166519 | snp | C/T | 3.43318e-05 | 0.00414303 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682810 | GACAAGGTGAGGGCC[C/T]CACGGGCCAGCCCGG | 54442 |
| rs764167230 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707238 | TTTTCTGGAGCAGGC[A/G]CCTGGTCAGGGACAC | 54442 |
| rs764174016 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703699 | GCCCAGAGCCTCCCT[C/T]GCTGGCCACCCGTTG | 54442 |
| rs764191093 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697529 | GTCGGCCTCCAGGCT[C/T]GGAGGGAAAATGCCA | 54442 |
| rs764195027 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706462 | AAGCTCTCTGCTCGG[A/G]AGCGTGGGGTGATTT | 54442 |
| rs764248284 | snp | A/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682178 | GCTCCGTAGTCTTGT[A/T]ATAAAAAGCATGTAC | 54442 |
| rs764303168 | snp | A/G | 1.64836e-05 | 0.0028708 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707335 | GGATGTGAGGGACAC[A/G]GTATTGACAGCTGAA | 54442 |
| rs764320022 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692967 | CCTGCTCCGTGGAGC[-/G]GGAAGCCCGGGTCTG | 54442 |
| rs764368091 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704533 | GACTCGCAGAGCTCA[C/G]TGAGAGCGCTTAGAC | 54442 |
| rs764411022 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704879 | GAGTGGGGCCAGAGG[C/T]CAGGCGCCTCTGGAC | 54442 |
| rs764542833 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693259 | GGAGTGGGGTCTGTT[C/T]GCCTCCTCCCTGTTC | 54442 |
| rs764550858 | snp | G/T | 1.66233e-05 | 0.00288295 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699783 | GCAGCAGTGGGACAT[G/T]GGTGGCCCGCCCTTA | 54442 |
| rs764905898 | snp | C/T | 1.68377e-05 | 0.00290148 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702492 | AGGTGAGTGCTGGGC[C/T]GGCCCTGGCCTGGGG | 54442 |
| rs764932407 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699816 | TGTGCCCATTGTCCT[G/T]GCAGGTGCCTGTGAA | 54442 |
| rs764992452 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700953 | CACCTCATCAGAATC[A/G]TGCCAGAGCCTCCCA | 54442 |
| rs765219382 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691027 | TGGCACCACGAGTAG[-/C]CCCCGCACACATTAG | 54442 |
| rs765316231 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682005 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 54442 |
| rs765384314 | snp | C/T | | | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697982 | AATTAGAGAACGAGA[C/T]AGCAAAACATCGCAG | 54442 |
| rs765425537 | snp | C/G | 9.58635e-05 | 0.00692261 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707443 | GATCATTTTTCTAGA[C/G]ATCTGGGTGTGAATC | 54442 |
| rs765458074 | snp | A/G | 4.00168e-05 | 0.0044729 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682508 | TATTAAAAGCCGGAC[A/G]CTTCCGGTGGAAGGG | 54442 |
| rs765658635 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704331 | GCATGGGCTGTGGGC[C/T]CTCGTCGCTGGTGTC | 54442 |
| rs765876587 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707104 | CCCTGTGTGGGGCCT[A/G]GAGATGTGCCAGACA | 54442 |
| rs765880446 | snp | C/G | 1.66835e-05 | 0.00288816 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699924 | TCGAGCAGGTGAGGG[C/G]CCCTGGCCAGCCTGG | 54442 |
| rs765969903 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691253 | CTCCACACGCCACTG[C/G]CTCCCCGCCCTGGTG | 54442 |
| rs766074923 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708231 | TCACGGTGAAAATTC[A/G]GGATGTTTACAGAGC | 54442 |
| rs766091252 | snp | C/T | 2.08153e-05 | 0.00322602 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682656 | GCTCGGCGCCCTGGC[C/T]CAGCGCCCTGGCAGC | 54442 |
| rs766101373 | snp | C/T | 2.85067e-05 | 0.00377525 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682590 | GTCGCCGGCCCGGGG[C/T]GGCATCGGGGCGGGG | 54442 |
| rs766143765 | snp | A/G | 1.6483e-05 | 0.00287076 | missense | KCTD5 | GRCh38.p7 | 16:2707313 | ATTTTGCAAGAACGA[A/G]GCTCAAGGATGTGAG | 54442 |
| rs766498189 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697484 | ACCCCACCCAGTGGC[A/G]TGGCCATGAGCAGGT | 54442 |
| rs766551471 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702168 | ATGCCATGCCACGGC[A/G]TGGGGTGCCGCCCCG | 54442 |
| rs766552919 | snp | G/T | 3.31576e-05 | 0.00407157 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697910 | CCTTATTCCAGGAGT[G/T]TTGGAGGAAGCAGAA | 54442 |
| rs766713733 | snp | G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681265 | GTTTTTAATCTTATA[G/T]AAGGTTATTTGCTGG | 54442 |
| rs766882747 | snp | G/T | 1.66272e-05 | 0.00288328 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702332 | TCACTGGGCTGCGTC[G/T]CAGGCTATGTCTCCT | 54442 |
| rs766930817 | in-del | -/AC | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709356 | TTTTTTCCTTAAGAG[-/AC]AGGGGTCTTGCTATG | 54442 |
| rs766953975 | snp | A/G | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709134 | AGCCCCACTGGCCGC[A/G]GCGGCTCACTCAGGG | 54442 |
| rs766971950 | snp | A/G | 2.09822e-05 | 0.00323893 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682543 | GTTGCGGGGCTTGCT[A/G]GGATCATGGCGGAGA | 54442 |
| rs767057526 | snp | C/T | 2.00684e-05 | 0.00316762 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682513 | AAAGCCGGACGCTTC[C/T]GGTGGAAGGGAGCTG | 54442 |
| rs767061788 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690416 | AGCCTGCTGGGCCCA[A/C]TCAATGCCAGCTTGG | 54442 |
| rs767230084 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708103 | TAGCAGTGTCGCCTC[A/G]CCCCTCCCACTGCGG | 54442 |
| rs767240624 | snp | A/C | 1.93755e-05 | 0.00311246 | missense | KCTD5 | GRCh38.p7 | 16:2682664 | CCCTGGCCCAGCGCC[A/C]TGGCAGCGTGTCCAA | 54442 |
| rs767276925 | snp | A/G | 1.70702e-05 | 0.00292144 | splice-donor-variant | KCTD5 | GRCh38.p7 | 16:2682801 | CTGGACTCAGACAAG[A/G]TGAGGGCCTCACGGG | 54442 |
| rs767313545 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706649 | CCTTGAGGAAGAGTT[C/T]TGAGGAGATTGGAGG | 54442 |
| rs767441972 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698137 | CTTGTCCTCTGTCAC[G/T]GCCCCAGTGCCTGCC | 54442 |
| rs767443661 | snp | A/G | 3.53619e-05 | 0.00420473 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707397 | AACTGCCATGTCCAG[A/G]AAGCTTGGCTGTGAG | 54442 |
| rs767463078 | in-del | -/ATCCAA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697546 | GAGGGAAAATGCCAG[-/ATCCAA]CCCCCAGCATACCAT | 54442 |
| rs767543754 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704557 | CTTAGACTCAAGGCC[A/G]CCATTTATTCCCAAG | 54442 |
| rs767631730 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681445 | GCCTCCGAGTAGCTG[A/G]GATTACGAGCGCCCA | 54442 |
| rs767646715 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704954 | ATCGCAAGATGCAGC[C/T]GCCTCACACGTGGAG | 54442 |
| rs767666996 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703637 | CATGTCTCTCGGAGG[A/C]CTGCGGCCAGCTCAC | 54442 |
| rs767794849 | snp | C/G | 0.000773694 | 0.0196532 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699351 | GAGTTTTAGGAAGCA[C/G]CTCAGCCTTCGGGAG | 54442 |
| rs767848546 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697257 | AAGACCACCCATGAG[A/G]AAGCCCTGAGGCAGG | 54442 |
| rs767906425 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706662 | TTTGAGGAGATTGGA[-/G]GGGTGGGGAGGGCAG | 54442 |
| rs768127817 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701152 | ACAATGTCTCCTGCC[C/T]GTGGTGGGCACCTGC | 54442 |
| rs768135825 | snp | C/T | 2.52669e-05 | 0.00355427 | missense | KCTD5 | GRCh38.p7 | 16:2682579 | TGCGAGCTCCTGTCG[C/T]CGGCCCGGGGCGGCA | 54442 |
| rs768201148 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697744 | CCTGCTGGGCTGACA[C/G]GTCTGCAGGAAGCCT | 54442 |
| rs768288830 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701921 | CAGACCCGCCCTGGC[C/T]GAACTCCTGGACAGC | 54442 |
| rs768471858 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691098 | CAAGACCCTGCCTAC[A/G]TGCTTGGAAGCGAGT | 54442 |
| rs768525431 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691897 | ATTTTGCACCCAGGC[C/T]GCTGGCCCCTGAGCA | 54442 |
| rs768572338 | in-del | -/G | 6.74218e-05 | 0.00580572 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702499 | TGCTGGGCCGGCCCT[-/G]GCCTGGGGCAGTCTT | 54442 |
| rs768575582 | snp | C/G | 0.000907085 | 0.0212772 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682533 | GAAGGGAGCTGTTGC[C/G]GGGCTTGCTGGGATC | 54442 |
| rs768651586 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700561 | GGGGCCCTTGCCCAC[A/G]ACCTGGCTGCCACTG | 54442 |
| rs768735412 | snp | C/G | 1.65949e-05 | 0.00288048 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702358 | CTCCTTGCAGTTGGT[C/G]AGCATCGGCTCCTCT | 54442 |
| rs768835939 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699555 | GTCGAGCCACAGGTG[C/T]TCTTGGGATTTCAGG | 54442 |
| rs768946085 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687527 | TGTTTTTGCAAGTAA[A/G]GTTTTACAGGAATGC | 54442 |
| rs768980235 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697188 | TAGGTGGCTGGGTGT[C/T]GTCCTGAGCTGCCAT | 54442 |
| rs769023599 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698328 | AGGTGGATGGCATCT[A/G]GTAGGGAGCAGAGGG | 54442 |
| rs769083663 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706271 | GAACAAGCCTGGGGT[A/G]GCATGCACCTCTCAC | 54442 |
| rs769142143 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684624 | CAAAAAATGAGCCAG[A/G]CGCGGTGGCGAGCAC | 54442 |
| rs769172350 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693136 | CTGGTGCCACTCTCA[C/G]TACCCACCCCAGGCC | 54442 |
| rs769204480 | snp | C/T | 3.38101e-05 | 0.00411143 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682761 | GAAATCCTTCCTGTA[C/T]CGCTTATGCCAGGCC | 54442 |
| rs769224600 | snp | C/T | 1.65963e-05 | 0.0028806 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707369 | ATGATTTACGTTTTC[C/T]CGAGATGTAATGAAC | 54442 |
| rs769224642 | snp | C/G | 2.37256e-05 | 0.00344416 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682644 | CTGCAGCGCTGGGCT[C/G]GGCGCCCTGGCCCAG | 54442 |
| rs769312504 | snp | C/T | 1.65056e-05 | 0.00287272 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707291 | TTATGCATTTGGTGT[C/T]TTTCAGATTTTGCAA | 54442 |
| rs769335361 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705290 | AGTTGACGAGAGCCG[C/T]CCGCACTCCATGCCA | 54442 |
| rs769546611 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707572 | TCTTGGGGGGGCCTC[A/G]CTCTGTTTTTTCCAA | 54442 |
| rs769587548 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2695779 | GGACGTGGCCACACC[G/T]TCAGGGGTTTCCTGA | 54442 |
| rs769654739 | in-del | -/A | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701637 | TTGGTCCAACTGCGC[-/A]AGGTCTTAGAGAGGC | 54442 |
| rs769751765 | snp | G/T | 0.000196792 | 0.00991753 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699252 | GGCGGGCGGCCCTGG[G/T]GGCTCACCATCACTC | 54442 |
| rs769795577 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691155 | GTGGGATTTGGGGGT[C/G]CTGGTTTAAGACCCT | 54442 |
| rs769878868 | snp | C/T | 2.37223e-05 | 0.00344392 | missense | KCTD5 | GRCh38.p7 | 16:2682570 | GAGAATCACTGCGAG[C/T]TCCTGTCGCCGGCCC | 54442 |
| rs769972024 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708052 | CCACAGGGCTTGCCG[C/T]GTGGAGACTGATCTG | 54442 |
| rs770024824 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698660 | GTGCCGCACTGTGGC[C/T]GCGGCTGCCATCAGA | 54442 |
| rs770026718 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708541 | TGCAGACTGACCACC[A/G]GCCTCCCGCCTGCAG | 54442 |
| rs770083272 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699422 | CTGGTAGCTGGGAGC[A/G]AGCTTCGTCTGGCAC | 54442 |
| rs770098354 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687403 | ATGCTGTCGCTGCAG[A/G]GCAGTTCCTCTTTCT | 54442 |
| rs770115484 | snp | C/G/T | 2.07174e-05 | 0.00321843 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682539 | AGCTGTTGCGGGGCT[C/G/T]GCTGGGATCATGGCG | 54442 |
| rs770220021 | snp | A/G | 1.65927e-05 | 0.00288029 | missense | KCTD5 | GRCh38.p7 | 16:2702365 | CAGTTGGTCAGCATC[A/G]GCTCCTCTTACAACT | 54442 |
| rs770311712 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701084 | AACAGGGCTGTCCCC[A/T]TGTGGCACCTGTGCT | 54442 |
| rs770438239 | snp | C/T | 3.52777e-05 | 0.00419972 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682842 | GGGTCCTGGCCTTCC[C/T]GGCCTGCGGCTCCTG | 54442 |
| rs770551693 | snp | C/T | 1.69608e-05 | 0.00291206 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682779 | CTTATGCCAGGCCGA[C/T]CCCGACCTGGACTCA | 54442 |
| rs770592318 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692165 | CTTGCAAAGCTCCAC[A/G]TCCCTGTGTCTGGAT | 54442 |
| rs770599646 | snp | C/G | 6.43025e-05 | 0.00566984 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707470 | AATCCTTTTTTGCCT[C/G]TGAGGTGGGTGGTGA | 54442 |
| rs770600144 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704738 | CCCCGTGGCTGATCC[C/T]TCCTGTGACCCAGGG | 54442 |
| rs770674018 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687888 | TGCTTGTTCTCCCTG[C/G]GCGTCAACTCGGCAG | 54442 |
| rs770780425 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707910 | GCCTTCTTCTGACAC[A/G]GGCTCCAACCCCACC | 54442 |
| rs770839019 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700863 | GTCCACCCTGGACCC[C/G]TAGGCCGGGGGCCGG | 54442 |
| rs770915359 | snp | A/G | 1.65603e-05 | 0.00287747 | missense | KCTD5 | GRCh38.p7 | 16:2699855 | ACCGTGTGCTGCAGT[A/G]CCAGGAGGAGGAGCT | 54442 |
| rs770942602 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706421 | CAGCTGTTGTGGGCC[A/G]CGCACAGTGAGGCTG | 54442 |
| rs771121008 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707860 | AAAGGCGGCTTCTGC[A/G]TCGTCACTGCTTCCC | 54442 |
| rs771291376 | snp | C/T | 2.78843e-05 | 0.00373381 | missense | KCTD5 | GRCh38.p7 | 16:2682624 | GGGGGCGGCCTGTGC[C/T]GCCGCTGCAGCGCTG | 54442 |
| rs771294066 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2682969 | GCTTGCCCCGATCCC[C/T]TACCCTGGGAGGGGA | 54442 |
| rs771311126 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698587 | CCGTCCCTGAGAGCT[A/G]AGCCCGCCCCCCCCA | 54442 |
| rs771322103 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681980 | TCCTGACCGCCTGAT[C/T]CTCCCGCCTCGGCCT | 54442 |
| rs771487863 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702651 | GTTCTCTCGACACAG[G/T]CTCCCAGTAAGCCCC | 54442 |
| rs771536000 | snp | A/G | 1.65905e-05 | 0.0028801 | missense | KCTD5 | GRCh38.p7 | 16:2702375 | GCATCGGCTCCTCTT[A/G]CAACTATGGGAACGA | 54442 |
| rs771691406 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691159 | GATTTGGGGGTCCTG[C/G]TTTAAGACCCTGGCA | 54442 |
| rs771728426 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703093 | CCTTCTGTTTTCTGC[A/G]GGGCAGGCAGCTGGG | 54442 |
| rs771732291 | snp | C/T | 3.33256e-05 | 0.00408187 | missense | KCTD5 | GRCh38.p7 | 16:2697990 | AACGAGACAGCAAAA[C/T]ATCGCAGGTGAGACA | 54442 |
| rs771770764 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690637 | CCCCCACGCCCAGCC[C/T]GCAGCATCTCACTGG | 54442 |
| rs771781624 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704173 | TGAAGTGGGGCAGCT[A/G]TGGCGGCTTCTTGAT | 54442 |
| rs771868615 | in-del | -/G | 1.70571e-05 | 0.00292032 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698031 | GCTGGAAGCTTGTAT[-/G]GCTGGTGTGAAGGAA | 54442 |
| rs771928837 | snp | C/G | 1.80585e-05 | 0.00300482 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707488 | AGGTGGGTGGTGAGA[C/G]ACGGGCCCAGCTGTC | 54442 |
| rs771944978 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693013 | TGGGGCGAACCCCAG[C/G]GCTGCAGCCCCAGGC | 54442 |
| rs772072606 | snp | A/C/T | 3.36453e-05 | 0.00410143 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699952 | TGGTGGCAGCCATGC[A/C/T]GCAGCTGAACTTGTG | 54442 |
| rs772246679 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705603 | GCTGCCAAATCCTGC[A/G]GCATCCCTGATGCGC | 54442 |
| rs772395906 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699347 | GATGGAGTTTTAGGA[A/G]GCAGCTCAGCCTTCG | 54442 |
| rs772439443 | snp | C/T | 1.69309e-05 | 0.0029095 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682732 | ACCACTCGGCAGACC[C/T]TGTGCCGGGACCCGA | 54442 |
| rs772455840 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706350 | CTGTGCCCGGCGAGG[A/G]CGTGGGCGTTGCTGC | 54442 |
| rs772460426 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697816 | GGGCCCTCATTGCAG[A/G]GGCAGGGGCAAGGGC | 54442 |
| rs772512869 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681107 | GATAAATGACTAGTA[C/T]GTCTTTCAGGTGGGT | 54442 |
| rs772582428 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681279 | AGAAGGTTATTTGCT[A/G]GCTATTGTTGGCCTC | 54442 |
| rs772709066 | snp | C/T | 1.69083e-05 | 0.00290755 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682764 | ATCCTTCCTGTACCG[C/T]TTATGCCAGGCCGAT | 54442 |
| rs772719335 | snp | C/T | 2.23028e-05 | 0.00333929 | missense | KCTD5 | GRCh38.p7 | 16:2682649 | GCGCTGGGCTCGGCG[C/T]CCTGGCCCAGCGCCC | 54442 |
| rs772740378 | in-del | -/A | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687740 | TTTGGTTCTTTTAGC[-/A]GCCCCCCTCCACGCC | 54442 |
| rs772787825 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703124 | GTGAAATGCAGGGAC[A/C]CCTGCCTCGTTTGCT | 54442 |
| rs772809388 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | KCTD5 | GRCh38.p7 | 16:2707302 | GTGTTTTTCAGATTT[C/T]GCAAGAACGAGGCTC | 54442 |
| rs772886064 | in-del | -/AT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688228 | TAAATAAATAAATAA[-/AT]ATATATATATATATA | 54442 |
| rs772978895 | snp | C/T | 0.00201861 | 0.0317054 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699277 | TCACTCCCAGGACCA[C/T]AGCTGCCTGGAGGGG | 54442 |
| rs772990935 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704246 | AGAGCCTCAGGAGGC[C/T]GTGGGGGATTGCGGG | 54442 |
| rs772991707 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708116 | TCGCCCCTCCCACTG[C/T]GGGCTCACGGGGAGC | 54442 |
| rs773009436 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708927 | AATTTATTCTAAGGG[A/G]ATATTTATACTTTTA | 54442 |
| rs773065072 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699609 | ACTTAGAAATAGAAA[C/T]ATTTTTGGAGGCGAA | 54442 |
| rs773195367 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703211 | TAAGCACGTTCTTAA[C/G]GTTGAGGCTCCAAGA | 54442 |
| rs773288832 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691198 | GGATGTGGAAATCTC[C/T]CATTGAAAGCTTCAA | 54442 |
| rs773466526 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705632 | GCTTAAGCCTCCCAG[A/G]CCAGCCGTGTCCTGC | 54442 |
| rs773619021 | snp | C/T | 2.37121e-05 | 0.00344318 | missense | KCTD5 | GRCh38.p7 | 16:2682571 | AGAATCACTGCGAGC[C/T]CCTGTCGCCGGCCCG | 54442 |
| rs773659369 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701155 | ATGTCTCCTGCCCGT[C/G]GTGGGCACCTGCCTC | 54442 |
| rs773685948 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703408 | CTGGGGCGAAGGCTC[A/G]GGGCATTGGCAAAGG | 54442 |
| rs773729295 | snp | C/T | 1.6591e-05 | 0.00288015 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702367 | GTTGGTCAGCATCGG[C/T]TCCTCTTACAACTAT | 54442 |
| rs773740114 | snp | A/G/T | 1.78036e-05 | 0.00298353 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682851 | CCTTCCCGGCCTGCG[A/G/T]CTCCTGCACACGCCC | 54442 |
| rs773810770 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707124 | TGTGCCAGACACCCC[A/G]GTGAAGGTCCTGGGC | 54442 |
| rs773862294 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701979 | GTCAGCTGGTCCCAG[C/G]CTCTTCCCTCCAGGT | 54442 |
| rs774009080 | snp | A/C | 1.69789e-05 | 0.00291362 | missense | KCTD5 | GRCh38.p7 | 16:2682785 | CCAGGCCGATCCCGA[A/C]CTGGACTCAGACAAG | 54442 |
| rs774241605 | in-del | -/AG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702765 | TGAGGGCTGTGTCTC[-/AG]GGGACCCAGGGTCCT | 54442 |
| rs774412699 | snp | A/G | 1.65625e-05 | 0.00287766 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699865 | GCAGTGCCAGGAGGA[A/G]GAGCTCACGCAGATG | 54442 |
| rs774419786 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706489 | ATTTCCCCTCCACCT[A/G]GTCTCTGGAGCTGCC | 54442 |
| rs774429295 | snp | G/T | 0.000657678 | 0.018122 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699313 | CAAGCGTGCCAGGCA[G/T]GTGGGGGATTAGGAG | 54442 |
| rs774471179 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708074 | ACTGATCTGTTCCAT[C/T]CGTTAGCGCGAGGTA | 54442 |
| rs774581641 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687562 | ATGCCCATTTGCTTA[C/T]GGATTGTGTGTGGCC | 54442 |
| rs774639282 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705487 | CAGGGAGTGCCACTC[A/G]TGCCGCCAGCCCTAG | 54442 |
| rs774641211 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693286 | GTTCCCTCCCTGCAG[C/T]GGCAGGTATCACGTG | 54442 |
| rs774835684 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697216 | CATGTGCCATATGTG[C/G]GTTCCTCTGGGGTCC | 54442 |
| rs774861391 | snp | C/T | 2.48537e-05 | 0.00352508 | missense | KCTD5 | GRCh38.p7 | 16:2682577 | ACTGCGAGCTCCTGT[C/T]GCCGGCCCGGGGCGG | 54442 |
| rs774951443 | snp | A/G | 2.11817e-05 | 0.00325429 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682546 | GCGGGGCTTGCTGGG[A/G]TCATGGCGGAGAATC | 54442 |
| rs775213606 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687629 | GCCTCGCCAGGGCTG[C/T]GGCCGTGATGGGGGC | 54442 |
| rs775324775 | snp | C/T | 0.000271334 | 0.0116444 | missense | KCTD5 | GRCh38.p7 | 16:2696035 | TTAACAAAGACCTCG[C/T]GGAGGAAGGTAAGCC | 54442 |
| rs775359992 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688152 | TGCCAGGTCAGTGCA[-/G]TCAGGAGAGGTTGTG | 54442 |
| rs775401267 | snp | G/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708150 | CGTCTGTCAGTGCCT[G/T]GTCACGCCTGGCATA | 54442 |
| rs775440507 | snp | C/T | 8.62106e-05 | 0.0065649 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707490 | GTGGGTGGTGAGAGA[C/T]GGGCCCAGCTGTCCA | 54442 |
| rs775515253 | in-del | -/C | 0.000370439 | 0.0136045 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699113 | CCTTAAGGTCAGGGA[-/C]CCAGGACCTCTGAAC | 54442 |
| rs775530442 | snp | A/T | 5.3445e-05 | 0.0051691 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707398 | ACTGCCATGTCCAGG[A/T]AGCTTGGCTGTGAGA | 54442 |
| rs775534178 | snp | C/T | 1.6582e-05 | 0.00287936 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699895 | GGTGTCCACCATGTC[C/T]GACGGCTGGAAGTTC | 54442 |
| rs775625914 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684287 | GAGCACTTGATTCCC[A/T]GTTGATGAACTTTAG | 54442 |
| rs775641995 | snp | C/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682039 | CCACCAGGCCCCGCC[C/G]TTATTATATAAATTT | 54442 |
| rs775660934 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704491 | ACACCTGCTTCCCAC[C/G]CCAGTCCCTCAAGAA | 54442 |
| rs775663084 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698670 | GTGGCCGCGGCTGCC[A/T]TCAGAAGTCTCGGTC | 54442 |
| rs775688623 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696797 | CGTGGAGTGACGGGG[A/G]CTGTGGCCCAGCCCT | 54442 |
| rs775851256 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699518 | GCGTGCGGAGCAGAC[A/G]TGGACGCTCTCGTGT | 54442 |
| rs775957264 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704757 | TGTGACCCAGGGCCC[C/T]ACCCTCCCTCCTGCA | 54442 |
| rs775971499 | snp | C/G/T | 5.28475e-05 | 0.00514018 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682581 | CGAGCTCCTGTCGCC[C/G/T]GCCCGGGGCGGCATC | 54442 |
| rs776013971 | snp | C/G | 4.98865e-05 | 0.00499407 | missense | KCTD5 | GRCh38.p7 | 16:2682637 | GCCGCCGCTGCAGCG[C/G]TGGGCTCGGCGCCCT | 54442 |
| rs776102395 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702995 | GGTGTCCTGCAGGCC[C/G]TGGGATTCTCAGGCT | 54442 |
| rs776107599 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701463 | GGACACAGGGGCTCC[-/G]GGGGGCATGGCCGTG | 54442 |
| rs776113908 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693208 | CCCAACCATGCTGCT[C/G]TCCTGCCATGCTGAG | 54442 |
| rs776176746 | snp | A/G | 1.68326e-05 | 0.00290104 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702490 | CAAGGTGAGTGCTGG[A/G]CCGGCCCTGGCCTGG | 54442 |
| rs776228011 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692197 | TGCCCAGCCCTGCTG[A/T]TACGGTGTCTTTAGG | 54442 |
| rs776282958 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693021 | ACCCCAGGGCTGCAG[C/T]CCCAGGCAGCCCCAC | 54442 |
| rs776292436 | snp | A/C | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709199 | GAGCTGGGCCATCCA[A/C]GGGGTGCCGGCTTGG | 54442 |
| rs776601556 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691046 | CGCACACATTAGGCC[C/G]ATCTGGAACATGTGG | 54442 |
| rs776631863 | in-del | -/CCT | 1.66601e-05 | 0.00288614 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707253 | GCCTGGTCAGGGACA[-/CCT]CCTCAGCCCAAGTCC | 54442 |
| rs776668376 | snp | G/T | 1.68267e-05 | 0.00290053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697861 | AGCGTGGATTCTTTG[G/T]TTTAGTTTGGTCTGG | 54442 |
| rs776691341 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688319 | GTGGTGGGGTGATCT[C/T]GGCTCACTGCAACCT | 54442 |
| rs776765472 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698592 | CCTGAGAGCTGAGCC[C/T]GCCCCCCCCACCCAA | 54442 |
| rs776772734 | snp | A/G | 2.06251e-05 | 0.00321125 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682536 | GGGAGCTGTTGCGGG[A/G]CTTGCTGGGATCATG | 54442 |
| rs776796742 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706422 | AGCTGTTGTGGGCCA[C/T]GCACAGTGAGGCTGG | 54442 |
| rs776820530 | snp | C/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681994 | TCCTCCCGCCTCGGC[C/G]TCCCAAAGTGCTGGG | 54442 |
| rs776870183 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699621 | AAATATTTTTGGAGG[C/T]GAACGAGGAAGCAGA | 54442 |
| rs776899477 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706952 | AGACTTAATTGGGGA[-/G]GGGGGACTGGACTGC | 54442 |
| rs776904157 | snp | A/C | | | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697922 | AGTGTTGGAGGAAGC[A/C]GAATTTTACAATATC | 54442 |
| rs776957296 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681301 | GTTGGCCTCTAGTTC[A/G]GCCTGTTATTTAAAT | 54442 |
| rs776991173 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707887 | TCCCGGCGCCATTCC[A/G]AGGCCGGGCCTTCTT | 54442 |
| rs777239196 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704308 | CCCTGGCTGGGCTGC[A/G]CAGGGCCGCATGGGC | 54442 |
| rs777335281 | snp | C/T | 5.64446e-05 | 0.00531216 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707464 | GGTGTGAATCCTTTT[C/T]TGCCTCTGAGGTGGG | 54442 |
| rs777387497 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693014 | GGGGCGAACCCCAGG[C/G]CTGCAGCCCCAGGCA | 54442 |
| rs777425217 | snp | C/T | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709253 | CACGGCCCATCCCTG[C/T]ACCCCACTCTGCCTG | 54442 |
| rs777458578 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699076 | GCCTTTGTCACTCAG[A/G]CATCCCTGGCATGAG | 54442 |
| rs777516487 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707656 | ATCGTGTGAAGGAAG[C/T]GTTCTTGGTGCTACA | 54442 |
| rs777941994 | snp | C/T | 1.72296e-05 | 0.00293505 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682701 | CCGACTCAACGTCGG[C/T]GGCACCTACTTCCTC | 54442 |
| rs778154927 | snp | G/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707729 | GCCGCAGCCGCGTCA[G/T]TGTCCAGCACGTCGT | 54442 |
| rs778191406 | snp | C/T | 0.000185374 | 0.00962562 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699160 | GTTTCCGTCCAGCCC[C/T]GTCTGCAGCCTGAGT | 54442 |
| rs778282084 | snp | A/G | 1.66626e-05 | 0.00288635 | missense | KCTD5 | GRCh38.p7 | 16:2702452 | ACCCCGTACGGTACG[A/G]CCAGCGAGCCCAGCG | 54442 |
| rs778358299 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698380 | ATGGCTGGAGGGAGA[C/T]AGCAGATGGGTCGTG | 54442 |
| rs778411707 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699014 | GTAGCATCTCACTGT[C/G]TTGCAGAATAAAGCA | 54442 |
| rs778499871 | snp | C/T | 2.64093e-05 | 0.00363372 | missense | KCTD5 | GRCh38.p7 | 16:2682583 | AGCTCCTGTCGCCGG[C/T]CCGGGGCGGCATCGG | 54442 |
| rs778502252 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681723 | ATTTTACAACTTTTT[C/T]CTGGCTTTATTACAA | 54442 |
| rs778559375 | snp | A/G | 2.0219e-05 | 0.00317948 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682522 | CGCTTCCGGTGGAAG[A/G]GAGCTGTTGCGGGGC | 54442 |
| rs778577712 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691907 | CAGGCTGCTGGCCCC[C/T]GAGCACAGGGATGGG | 54442 |
| rs778770252 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704676 | TTCCTTGGTGGTGTT[A/G]GGGCTCCATTGCGTA | 54442 |
| rs778859560 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701492 | TGAGTGCTCCCAGGG[G/T]TACCCTTAGCTGCTT | 54442 |
| rs778883555 | in-del | -/ATAAATAAATAT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688220 | TTATTAAATAAATAA[-/ATAAATAAATAT]ATAAATAAATATATA | 54442 |
| rs778951943 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708091 | GTTAGCGCGAGGTAG[C/T]AGTGTCGCCTCGCCC | 54442 |
| rs779190978 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683229 | GGCGTTGTTTCACAT[G/T]CTGGACGTTTGAATT | 54442 |
| rs779284966 | snp | A/C | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681081 | AGCTGTTCCTTCACA[A/C]CATGAAATAGGATAA | 54442 |
| rs779329352 | snp | A/G | 1.64868e-05 | 0.00287109 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707341 | GAGGGACACAGTATT[A/G]ACAGCTGAAGAAATG | 54442 |
| rs779338934 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687801 | AAAGCCTGGGGAAGA[A/G]CCTGCCTGCCTGGCG | 54442 |
| rs779369840 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707077 | GAGGGGCTGCCATGC[A/C]CAGTGAGCGCTCCCT | 54442 |
| rs779415409 | snp | C/G | 5.4739e-05 | 0.0052313 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682626 | GGGCGGCCTGTGCCG[C/G]CGCTGCAGCGCTGGG | 54442 |
| rs779633154 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698208 | TCCATTCATCCTGCC[C/T]GGCCCAGACTCTGGG | 54442 |
| rs779694301 | snp | C/G | 1.66123e-05 | 0.00288199 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699792 | GGACATGGGTGGCCC[C/G]CCCTTACCTGTGCCC | 54442 |
| rs779830344 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702749 | CTCTTAGGAATGCCA[A/C]TGAGGGCTGTGTCTC | 54442 |
| rs779852810 | snp | C/T | 2.29946e-05 | 0.00339069 | missense | KCTD5 | GRCh38.p7 | 16:2682564 | ATGGCGGAGAATCAC[C/T]GCGAGCTCCTGTCGC | 54442 |
| rs779990339 | snp | G/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708354 | ACCTGCACGGGCTCT[G/T]CCCGACATGCCGTGG | 54442 |
| rs780016325 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703905 | CCCTGAGAGCCCCAG[C/T]TCAGTCACAAGGAGG | 54442 |
| rs780283657 | snp | A/G | 1.68937e-05 | 0.0029063 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682746 | CCTGTGCCGGGACCC[A/G]AAATCCTTCCTGTAC | 54442 |
| rs780449883 | snp | C/T | 1.7297e-05 | 0.00294078 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682823 | CCTCACGGGCCAGCC[C/T]GGAGGGTCCTGGCCT | 54442 |
| rs780475754 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705315 | ATGCCAGCTGTAGAT[C/T]CTCAGTAGCACTGTC | 54442 |
| rs780528519 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701216 | ACTTCTGGGTGGATT[C/T]CAAACCCATTGCAAA | 54442 |
| rs780540974 | in-del | -/GAG | | | splice-donor-variant | KCTD5 | GRCh38.p7 | 16:2682802 | GGACTCAGACAAGGT[-/GAG]GAGGGCCTCACGGGC | 54442 |
| rs780581914 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687686 | CTGTCGTTAACCACC[A/C]GGCATCCCAGGGACT | 54442 |
| rs780760443 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705164 | CCAGGGGCACCCAGG[A/G]AGTGGCTCAGATTAA | 54442 |
| rs780760622 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704742 | GTGGCTGATCCCTCC[C/T]GTGACCCAGGGCCCC | 54442 |
| rs781102831 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697630 | ACCTGGCGGGTCACT[A/G]GAGGTCACTCAAGGT | 54442 |
| rs781123652 | snp | A/C/G | 9.41473e-05 | 0.00686047 | synonymous-codon, missense | KCTD5 | GRCh38.p7 | 16:2682569 | GGAGAATCACTGCGA[A/C/G]CTCCTGTCGCCGGCC | 54442 |
| rs781159218 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701618 | GCGGGCTGCTCTCCC[A/G]GCCGTTGGTCCAACT | 54442 |
| rs781413339 | snp | C/G | 1.69052e-05 | 0.00290728 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702506 | CCGGCCCTGGCCTGG[C/G]GCAGTCTTGGGTGGG | 54442 |
| rs781429770 | snp | A/G | 3.3295e-05 | 0.00408 | missense | KCTD5 | GRCh38.p7 | 16:2702446 | CACAACACCCCGTAC[A/G]GTACGGCCAGCGAGC | 54442 |
| rs781571774 | snp | A/G | 4.97047e-05 | 0.00498496 | missense | KCTD5 | GRCh38.p7 | 16:2697966 | AACTTGTAAAGGACA[A/G]AATTAGAGAACGAGA | 54442 |
| rs781579495 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699385 | CAAGTCCAGGCTGCC[A/G]CGCAAGTTCAAGAGC | 54442 |
| rs781615294 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687360 | TCGGCATTCTCGCCT[C/G]CAGACTTCTGCGGGT | 54442 |
| rs781629063 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2682974 | CCCCGATCCCCTACC[C/G]TGGGAGGGGAGGGTG | 54442 |
| rs796151693 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698211 | ATTCATCCTGCCCGG[C/G]CCAGACTCTGGGAGC | 54442 |
| rs796222844 | in-del | -/TT | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681746 | ATTACAAAAACTTTC[-/TT]TTTTTTTTTTTTTGA | 54442 |
| rs796302047 | in-del | -/TTTTC | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2689674 | CATTCCTCACTGCCG[-/TTTTC]TTTTCTTTTTTTTTT | 54442 |
| rs796394163 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700511 | TGGCTTGTCATCGGG[-/G]ACCTCAGGACACGTG | 54442 |
| rs796409853 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683469 | AGGAATCTTTCAATC[C/T]GCTTTCTAATTGGCT | 54442 |
| rs796517817 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687827 | TGGCGCCATGGGAGG[C/G]GTCCTTGTAGCAAAG | 54442 |
| rs796551809 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682428 | GAACTTCCGCCTACC[A/G]CGTGACGCCGGGGCG | 54442 |
| rs796856730 | multinucleotide-polymorphism | CA/GG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705463 | AAGAGCCCCTCCTGG[CA/GG]GCTGGGCAGGGAGTG | 54442 |