SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11986 | snp | A/G | 0 | 0 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708739 | TAAGTCTGCCTTCTA[A/G]AAAGGCTTTTATAAA | 54442 |
rs732055 | snp | A/G | 0.470521 | 0.117772 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700191 | ACACAGAGGTGCCAG[A/G]TGATGCGAAGAAAGC | 54442 |
rs732057 | snp | C/G | 0.309154 | 0.242901 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700617 | GGGAGGGCTGGGTGA[C/G]GTCACTGTCCCCACC | 54442 |
rs732058 | snp | C/T | 0.332568 | 0.235971 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700870 | AGTCACCCCGGCCCC[C/T]GGCCTAGGGGTCCAG | 54442 |
rs739717 | snp | A/G | 0.478603 | 0.101197 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702153 | GGAAGAGCTCGCCCC[A/G]TGCCATGCCACGGCG | 54442 |
rs757168 | snp | C/G | 0.234109 | 0.249494 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700209 | ACGCCAGTCCCCTCC[C/G]TCACACAGAGGTGCC | 54442 |
rs1859137 | snp | C/T | 0.454544 | 0.143743 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700454 | AGCACTCAGGTGGCT[C/T]CCGTGGAAGCTGCTG | 54442 |
rs2074368 | snp | C/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695469 | CCTACATGCAGGAAC[C/G]GGGGGTCAGGGTGAC | 54442 |
rs2335152 | snp | C/G | 0.117886 | 0.21224 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696842 | GCTGTGAGCCATGAT[C/G]CCCACTCCTGTCTCT | 54442 |
rs2335153 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696882 | AATGTCTTTCACATG[C/T]ACTCTCTCTGGTCGC | 54442 |
rs2335154 | snp | C/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696936 | TGGAGCCGCTCGAGT[C/T]GAGGCTTCGCTTTAT | 54442 |
rs2335155 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696986 | GATTGGCTCAGAAAC[A/G]GGCGCTAGACACAGA | 54442 |
rs2335156 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696990 | GGCTCAGAAACGGGC[A/G]CTAGACACAGACCAA | 54442 |
rs2907052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696543 | CCAACGCGTGTGGGC[A/G]CCGTCCCTGCACCAC | 54442 |
rs2965989 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696747 | TGGGCCTCTGGGCCT[C/G/T]GGCATCTGCCTGCCT | 54442 |
rs3030700 | in-del | -/GA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700642 | CCCTCCCTGTCCTGA[-/GA]GTTTCCTCTGTCACT | 54442 |
rs3030702 | in-del | -/C/CC | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700814 | TGGAGCCCCCCCCCC[-/C/CC]TTAAAATGTCACTAA | 54442 |
rs3032675 | in-del | -/CT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696916 | GCAGCCGCTTGTGTT[-/CT]GTCGTGGAGCCGCTC | 54442 |
rs3094470 | snp | C/T | 0.320335 | 0.239902 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704259 | TCCAGCTCTGGCCCC[C/T]GCAATCCCCCACGGC | 54442 |
rs3094471 | snp | A/G | 0.333722 | 0.235565 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703179 | AGGAAATGCCACCAG[A/G]ATGGGTCACCTGTGG | 54442 |
rs3094473 | snp | C/T | 0.470853 | 0.11715 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699194 | GGTGGCCCCACATCC[C/T]GGACAGTCACTACGG | 54442 |
rs3094474 | snp | A/G | 0.308661 | 0.24302 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698062 | GGCAGCCGGTCGGGG[A/G]AGTAAAGGGGAGCCC | 54442 |
rs3094475 | snp | A/G | 0.487232 | 0.078872 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697856 | CCAAACTAAACCAAA[A/G]AATCCACGCTTTACA | 54442 |
rs3094476 | snp | C/T | 0.428484 | 0.175052 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697615 | CAGTGACCCGCCAGG[C/T]ATGGAGCCGCTGCTT | 54442 |
rs3094477 | snp | C/T | 0.471388 | 0.116136 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697076 | CACAGCCCCCTTCTC[C/T]AGCACCCAGGGCGTG | 54442 |
rs3094478 | snp | C/T | 0.308908 | 0.242961 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697049 | CGTGAGTGGCTGCAT[C/T]GGGGCGGGATAGAGG | 54442 |
rs3094479 | snp | C/T | 0.45946 | 0.136478 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696660 | GGGGGAGCAGGGCCA[C/T]GCCCGCACGCAGGTG | 54442 |
rs3112710 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680955 | CCACATAGCCTAACC[A/G]TCTGGCAGAATGACT | 54442 |
rs3112711 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680956 | CACATAGCCTAACCG[C/T]CTGGCAGAATGACTA | 54442 |
rs3112712 | snp | C/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683297 | TTCCCTGGTGACTTG[C/T]ATTTAGAGAGTTGGC | 54442 |
rs3112713 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683374 | TTAGAAGATGCGTCC[A/G]TAGTATATAGTATGA | 54442 |
rs3112714 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683384 | CGTCCGTAGTATATA[C/G]TATGATTTTTCGAAG | 54442 |
rs3112715 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683386 | TCCGTAGTATATAGT[A/G]TGATTTTTCGAAGGG | 54442 |
rs3112716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683447 | GATGTCCAGGAAGGG[C/T]CAGGTAAGGAATCTT | 54442 |
rs3112724 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696590 | CTGTGTGCTGCGGTG[A/C]TGGCTTGGCTCAGAA | 54442 |
rs3112725 | snp | C/G | 0.470811 | 0.117228 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697098 | GGGGCTGTGCGGGAC[C/G]CATGCGGGGCCGGGA | 54442 |
rs3112726 | snp | C/T | 0.444267 | 0.157354 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698698 | GTCCACGTAGAGCCC[C/T]GGGCCCTGTGCAGAC | 54442 |
rs3112727 | snp | C/T | 0.304688 | 0.243945 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699529 | AGACGTGGACGCTCT[C/T]GTGTCGTCATGTCGA | 54442 |
rs3112728 | snp | C/T | 0.311859 | 0.242226 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701172 | TGGGCACCTGCCTCC[C/T]GGGGCAGCTTCAGGT | 54442 |
rs3743929 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709200 | GCCAAGCCGGCACCC[C/T]GTGGATGGCCCAGCT | 54442 |
rs3785340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706546 | GAGGACAGGCTCAGG[C/T]GCTGGCCAATGCTGC | 54442 |
rs3785341 | snp | A/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705045 | CAAACCCCCACGCCC[A/G]GTGACCTTCCAGTGA | 54442 |
rs3785342 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703616 | GAGAGACATGCTTGG[A/C]GGCCCCACCCCTCTG | 54442 |
rs3826244 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704727 | AGGAGGGATCAGCCA[C/T]GGGGGCAGGCGGTGG | 54442 |
rs3837778 | in-del | -/GGCCCCCAGCC | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703512 | CAGAGGCCCCCAGCC[-/GGCCCCCAGCC]AAGAGTCTGCGGTTG | 54442 |
rs3842363 | in-del | -/AAG | 0.00478275 | 0.0486673 | cds-indel | KCTD5 | GRCh38.p7 | 16:2707897 | AGCCCGTGTCAGAAG[-/AAG]GCCCGGCCTCGGAAT | 54442 |
rs4045847 | in-del | -/TCGCTTGG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696894 | ATGTACTCTCTCTGG[-/TCGCTTGG]GCAGCCGCTTGTGTT | 54442 |
rs4296261 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700695 | TCCATGGCCCAGTGC[A/G]CCTGCCAGGTTGTGG | 54442 |
rs4785900 | snp | C/G | 0.284209 | 0.247648 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684324 | TAAGGTGGTTGATCC[C/G]TTTGCTTTACTGTTC | 54442 |
rs4786320 | snp | G/T | 0.167809 | 0.236103 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705879 | TGCAGGTCTCCAGGG[G/T]GTCTCCTGCCCTCAT | 54442 |
rs5815130 | in-del | -/AG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700639 | CCTCCCTGTCCTGAG[-/AG]TTTCCTCTGTCACTT | 54442 |
rs5815131 | in-del | -/C | 0.402201 | 0.19833 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700804 | TGGAGCCCCCCCCCC[-/C]TTAAAATGTCACTAA | 54442 |
rs7188619 | snp | C/T | 0.00874735 | 0.0655527 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2709016 | AAATAGCAAATAAAA[C/T]TGTGTATTTATGAAT | 54442 |
rs7188658 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698595 | GAGAGCTGAGCCCGC[C/T]CCCCCCACCCAAGCT | 54442 |
rs7194693 | snp | C/G | 0.481473 | 0.0944461 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689766 | cactgcaacggggct[C/G]tcaggttcaagtgat | 54442 |
rs7201996 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705567 | CAGGACCAGTGCGGC[A/G]GACAGCAGACCCCTA | 54442 |
rs7206555 | snp | A/G | 0.0174175 | 0.0916809 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709409 | tgctgggctcaagtg[A/G]tcctcctgcctcagc | 54442 |
rs8044323 | snp | A/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698949 | ATGACGCAGGTGGGC[A/G]GGAAATGGTGCAGGT | 54442 |
rs8048298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698851 | CTGCGTCCCGCGCCC[C/T]GGGTCACCTTGTCCA | 54442 |
rs8048336 | snp | C/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698912 | CTGTGTGGGCACTCC[C/G]TGCCTCAGTCTACCT | 54442 |
rs8049286 | snp | C/T | 0.102726 | 0.202016 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705187 | CAGATTAAGTGTGAA[C/T]GTCATGGTGAGCTCC | 54442 |
rs8057370 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681358 | cactctgtcgcccag[A/G]ctagagtgcagtggc | 54442 |
rs8059207 | snp | A/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699237 | GAGCAGCTCCATGCA[A/G]GCGGGCGGCCCTGGT | 54442 |
rs8059210 | snp | A/G | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699240 | CAGCTCCATGCAGGC[A/G]GGCGGCCCTGGTGGC | 54442 |
rs8063137 | snp | C/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699134 | ACCTCTGAACCCCTT[C/T]TCACTGCTGCGTTTC | 54442 |
rs8063286 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699188 | AGTCCTCCGTAGTGA[C/G]TGTCCAGGATGTGGG | 54442 |
rs9926188 | snp | C/T | 0.427727 | 0.175821 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692732 | gggacctaccccctt[C/T]ttcccaggaatctat | 54442 |
rs9935912 | snp | A/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688247 | TATATATATATATAT[A/T]TATTTATTTATTTAT | 54442 |
rs9941296 | snp | A/G | 0.0558544 | 0.157504 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709498 | TTTGAAAGTCCTGAT[A/G]CCTCAAGTTAGCATC | 54442 |
rs10500324 | snp | A/G | 0.308414 | 0.24308 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691811 | GGCTGCTCCTTTCAA[A/G]TCTCTTCCTAACTGG | 54442 |
rs11077332 | snp | A/G | 0.465996 | 0.12588 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684980 | GGAATCAATTCTTTG[A/G]GCGAGGGGTAATTAA | 54442 |
rs11077336 | snp | A/G | 0.459004 | 0.137176 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692019 | CCTGGTCCCTCTGTC[A/G]GGAGCCTGAGCTCCA | 54442 |
rs11552505 | snp | A/C | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708633 | TGGTTAATCAGGTGA[A/C]TGGCAAAGAGGAGGA | 54442 |
rs11642384 | snp | G/T | 0.122411 | 0.214991 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693417 | AAGCTGCCTCCTAAA[G/T]GGGGTGTTTAATGGA | 54442 |
rs11644881 | snp | A/G | 0.490563 | 0.0680388 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690840 | GCTGCCTTTGTCTCC[A/G]TGAGCCTCGGAGTAT | 54442 |
rs11645410 | snp | C/T | 0.494526 | 0.0520291 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687070 | CTCTGCGATGGTCCC[C/T]GCGGTGCTGGGGGCT | 54442 |
rs11646634 | snp | C/T | 0.208474 | 0.246527 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693451 | GCCAGCCCCGCCCAG[C/T]GGTAGGAGTGGCCAA | 54442 |
rs11860950 | snp | C/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702879 | CTGAGTGCAGGGACA[C/T]GGGGGTCCAGTTGTC | 54442 |
rs12149376 | snp | C/T | 0.178785 | 0.239642 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688349 | TCTGCCTCCTGGGTT[C/T]AAGCATTTCTCCTGC | 54442 |
rs12149789 | snp | A/G | 0.43088 | 0.172575 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690266 | GGCTGTGTGTGCCCT[A/G]GCTCGGCGCTGTCTG | 54442 |
rs12448477 | snp | C/T | 0.286303 | 0.24735 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684531 | agcactttgggaggc[C/T]gaggcaggcggatca | 54442 |
rs12926029 | snp | G/T | 0.335788 | 0.23482 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689714 | GACAGAGGCTCACTG[G/T]ATCGCCCAGGCTGGA | 54442 |
rs13331521 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687396 | GGAGGAAATGCTGTC[A/G]CTGCAGGGCAGTTCC | 54442 |
rs13331631 | snp | A/C/G | 0.0360663 | 0.129354 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687634 | GCCAGGGCTGTGGCC[A/C/G]TGATGGGGGCGCCTG | 54442 |
rs13331679 | snp | G/T | 0.110167 | 0.207236 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687662 | CTGCTGCCTGGTCTC[G/T]CCCCGGCCCTGTCGT | 54442 |
rs13333623 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706895 | GGTCCGGGCGTCGGG[A/G]TGGGGGTGGGGGCTG | 54442 |
rs13337854 | snp | A/G | 0.227664 | 0.249 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702687 | CCTCCCAGCCTGCAT[A/G]CAGAGCTGCTCCTGG | 54442 |
rs17136030 | snp | C/G | 0.014814 | 0.0847794 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708214 | GGAGCTGAAGGTCTG[C/G]GTCACGGTGAAAATT | 54442 |
rs17598822 | snp | A/G | 0.482757 | 0.0912364 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696544 | TGGTGCAGGGACGGC[A/G]CCCACACGCGTTGGG | 54442 |
rs28379781 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697685 | GTGTTCAGTCCACAC[A/G]TCGGCCCTCTCACCA | 54442 |
rs28536680 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693182 | CAGCTCTGCATCGGG[C/G]CCCCTCTCCACCCAA | 54442 |
rs28567711 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688228 | ATAAATAAATAAATA[A/T]ATATATATATATATA | 54442 |
rs28572556 | snp | C/G/T | 0.0744748 | 0.178019 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680637 | TGGGGTCCCTTCTTA[C/G/T]GCAGCACACGTGGCA | 54442 |
rs28576266 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688224 | TTAAATAAATAAATA[A/T]ATAAATATATATATA | 54442 |
rs28580368 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688239 | AATAAATATATATAT[A/T]TATATATTTATTTAT | 54442 |
rs28593320 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688243 | AATATATATATATAT[A/T]TATTTATTTATTTAT | 54442 |
rs28711015 | snp | G/T | 0.499946 | 0.00519141 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689536 | GTCTCCGAGCACCGG[G/T]AATGACTGAGAGCCG | 54442 |
rs34064394 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700808 | GTACTTGGAGCCCCC[-/C]CCCCCCTTAAAATGT | 54442 |
rs34835609 | in-del | -/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681723 | ATTTTACAACTTTTT[-/T]CTGGCTTTATTACAA | 54442 |
rs35317991 | snp | A/G | 0.428786 | 0.174744 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694030 | AGGTAGCAGTGAGCC[A/G]TGAATAATTCCTGAG | 54442 |
rs35526200 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703418 | GCTCGGGGCATTGGC[-/C]AAAGGGTGTTGAGTG | 54442 |
rs35550972 | in-del | -/A | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682300 | GGCGCTCGTGCACCG[-/A]CTCGTGGGAGGTCGA | 54442 |
rs35702964 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702203 | TCGTGCAGGTGTTCC[-/C]GGGGATTTGTTTTCC | 54442 |
rs36059005 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693421 | TGCCTCCTAAAGGGG[-/G]TGTTTAATGGAAAAG | 54442 |
rs55644829 | snp | A/G | 0.158632 | 0.232706 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684131 | ATGTTTTACTGTTTG[A/G]TTTTTCTTTTTAAAT | 54442 |
rs55839427 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698752 | CCGCTGGCCACCTAG[A/C]GACTTGCCCAGTTCC | 54442 |
rs55857409 | snp | A/G | 0.176219 | 0.238865 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696695 | CCGTGTCTGCGCATC[A/G]GTCTGCACTGGGCAG | 54442 |
rs56046076 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693587 | TGCTGTGCAGTTTCC[A/G]CCGATGGCCGTCCCC | 54442 |
rs56092617 | snp | C/T | 0.247905 | 0.249991 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681742 | GCTTTATTACAAAAA[C/T]TTTCTTTTTTTTTTT | 54442 |
rs56117069 | in-del | -/ATTT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688265 | TTTATTTATTTATTT[-/ATTT]GAGACGGAGTCTTGC | 54442 |
rs56119422 | in-del | -/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696762 | CGGCATCTGCCTGCC[-/T]CCTCCGAGTTCACGC | 54442 |
rs56275583 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708959 | ACTTTTTTAGGTATC[A/G]TATTTTATCAGCTTA | 54442 |
rs56317084 | in-del | -/AATAAATATATA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688224 | TTAAATAAATAAATA[-/AATAAATATATA]TATATATATATTTAT | 54442 |
rs56387515 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682943 | GCTCCCTTGTCGCCA[C/G]CTCCTCCCCAGCTTG | 54442 |
rs56403003 | in-del | -/G | 0.235564 | 0.249583 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700508 | TTGTGGCTTGTCATC[-/G]GGGACCTCAGGACAC | 54442 |
rs56693563 | snp | A/T | 0.130008 | 0.219321 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697101 | GCTGTGCGGGACCCA[A/T]GCGGGGCCGGGAAGC | 54442 |
rs56746195 | snp | C/T | 0.0498117 | 0.149749 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708550 | ACCACCGGCCTCCCG[C/T]CTGCAGGTCAGAGGC | 54442 |
rs57515743 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691671 | GAGGCACTGGGGCGG[C/T]GGGGGTGTGGAGCGG | 54442 |
rs57652537 | snp | G/T | 0.121369 | 0.214369 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697272 | GAAGCCCTGAGGCAG[G/T]ACCTGTGGAATCTGC | 54442 |
rs57669589 | snp | G/T | 0.121717 | 0.214577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697183 | CCATGTAGGTGGCTG[G/T]GTGTTGTCCTGAGCT | 54442 |
rs58041187 | snp | A/G | 0.121717 | 0.214577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697157 | TTGTCTCTATCCTGC[A/G]TGGCCCTGTCCCATG | 54442 |
rs58348343 | snp | C/T | 0.267364 | 0.249396 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693819 | CGGCCCCGAGCTACA[C/T]GAGCTGGTCTCCCCC | 54442 |
rs59959172 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704460 | TGTAGCAAGTGAAGG[C/T]GGTCCACACATGAGC | 54442 |
rs61312332 | snp | C/T | 0.0225045 | 0.103662 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709114 | GCTGCCCCTCCAAGC[C/T]GCCCAGCCCCACTGG | 54442 |
rs61411456 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687132 | GTCCTCAGCAAACCT[A/G]TGCTCACCTCTTTAT | 54442 |
rs61433364 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687447 | CAGCCTTCAGTGGCT[C/G]TCGTCCAGCAGGGCA | 54442 |
rs62034251 | snp | G/T | 0.15665 | 0.231917 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698372 | CAGCCAGCATGGCTG[G/T]AGGGAGACAGCAGAT | 54442 |
rs67187827 | snp | C/T | 0.274929 | 0.248754 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686871 | AAGAGAAGTGGGGAT[C/T]ACGTCTAGTGGAGAT | 54442 |
rs71386685 | snp | C/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691240 | GTGAGAGCAGCACCT[C/T]CACACGCCACTGCCT | 54442 |
rs71386686 | snp | C/G | 0.245061 | 0.249951 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695101 | GGCCGGGCCACTGGG[C/G]CTCTTGTGCTTTGTG | 54442 |
rs71394744 | in-del | -/TT | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688244 | ATATATATATATATA[-/TT]TATTTATTTATTTAT | 54442 |
rs72768746 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698396 | AGCAGATGGGTCGTG[C/T]GGGTCTGCGCAGGCG | 54442 |
rs73494243 | snp | G/T | 0.116838 | 0.211584 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697654 | TCAAGGTTACCTGGG[G/T]TGACCTGAGCTGGAG | 54442 |
rs73494249 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698530 | TGGGCTCTGCCCAGT[A/G]CCTCCTGTGGAGGGG | 54442 |
rs73494261 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703866 | TTCCATTTGAGTCTC[A/G]GATCTAGGAGGCGAC | 54442 |
rs73494263 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706090 | CCCCTCGCACAGGGG[A/G]ATGGGCTCCTCCGAG | 54442 |
rs74003056 | snp | A/G | 0.245631 | 0.249962 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680854 | ACCTGAATTTTCCCC[A/G]TAACTCATTTCTTCC | 54442 |
rs74003058 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687789 | GGCATGGTCTTTAAA[A/G]CCTGGGGAAGAACCT | 54442 |
rs74003059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696937 | GGAGCCGCTCGAGTC[A/G]AGGCTTCGCTTTATC | 54442 |
rs74003062 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698295 | AGGGCCCCATGAGGG[C/G]CGGTCGGGGAGACCC | 54442 |
rs74003063 | snp | C/G | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707116 | CCTGGAGATGTGCCA[C/G]ACACCCCGGTGAAGG | 54442 |
rs74428169 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693484 | CACGGCAGCGGCCTA[C/T]CCCTGCCTGCCCGTC | 54442 |
rs74758824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691520 | AGGGCTGTGGGGGCA[C/G]CTGCAGGCCCGGCGC | 54442 |
rs74966633 | snp | A/C | 0.120674 | 0.21395 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687055 | TCTTCTATTCTGGAC[A/C]TCTGCGATGGTCCCT | 54442 |
rs74969856 | snp | C/T | 0.0209421 | 0.100162 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707936 | CCACCTGACCAAGCC[C/T]GGGACAGTCAAGGCT | 54442 |
rs75091047 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700055 | GGTGCTCACGGCAGC[A/G]ACCTGTGCCCTGTTT | 54442 |
rs75370611 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687506 | CAGAAAGCTGGTCCA[A/C]CTGCCTGTTTTTGCA | 54442 |
rs75440502 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698445 | TATTGGGAAGAGGGG[C/T]GGCTCGCCACAGACA | 54442 |
rs75461256 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702624 | TTGGACACACGGTCT[C/T]CCGTGGGACAGGTTC | 54442 |
rs76457605 | snp | A/C | 0.0418186 | 0.138422 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682865 | GGCTCCTGCACACGC[A/C]CTGCTTCGTGCGGAG | 54442 |
rs76498482 | snp | G/T | 0.0988009 | 0.199095 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707525 | CAGACGTCCCCAAGT[G/T]GGGGGAGCACGGCGG | 54442 |
rs76556315 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691531 | GGCAGCTGCAGGCCC[A/G]GCGCGCCGAGTCCAC | 54442 |
rs76580822 | snp | A/C | 0.0197687 | 0.0974348 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708147 | TGGCGTCTGTCAGTG[A/C]CTTGTCACGCCTGGC | 54442 |
rs76887572 | snp | A/G | 0.0146672 | 0.084371 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708468 | GTCTGGGGACTCGGC[A/G]TGCAGGGCGGGCTCC | 54442 |
rs77212820 | snp | C/T | 0.0640965 | 0.167152 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690330 | TCTGTGGTTTGGCAA[C/T]TGTCCTGCCCGGCCT | 54442 |
rs77397807 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700289 | ACAGCTCACTCCATC[A/G]GAGCATATGGAGGCC | 54442 |
rs77625825 | snp | C/T | 0.111224 | 0.207945 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687160 | TATCAGGTGCCTCAC[C/T]TGAAGCCCTTTAGAC | 54442 |
rs77661775 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704193 | GGCTTCTTGATGGGG[G/T]TGGTGTCAGCAGTGC | 54442 |
rs77844870 | snp | G/T | 0.0298908 | 0.118541 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708282 | GCCGCTCTCTCATTT[G/T]CTTTGTATAACTATG | 54442 |
rs77915210 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699452 | CTGGCTCTCAGGGCC[C/T]TGCTTGCCAGAGCCT | 54442 |
rs77958764 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690398 | AGATGGGTGGCTCAG[C/G]CCAGCCTGCTGGGCC | 54442 |
rs78206812 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697039 | CACCGGTCTGCCTCT[A/G]TCCCGCCCCGATGCA | 54442 |
rs78376026 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691350 | AGGAACCCATGGGAA[A/G]AAACGGCCGGAGAGC | 54442 |
rs78381263 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698880 | CAGTCTGCTTTTTTC[C/T]CTGTTGTGTGACCGG | 54442 |
rs78577892 | snp | A/C/G | 0.0644693 | 0.167566 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692405 | AGGTCGGCTCATTCA[A/C/G]TTGGCAGCTCTCAGC | 54442 |
rs78651644 | snp | C/T | 0.283947 | 0.247685 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683835 | CAGAAAGGTTCGGAT[C/T]CCTCTTCAAGTTTGA | 54442 |
rs78846532 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704161 | AAATACCTGCTCTGA[A/T]GTGGGGCAGCTATGG | 54442 |
rs78851439 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693220 | GCTCTCCTGCCATGC[C/T]GAGGGCAGTGGGCTA | 54442 |
rs79178474 | snp | A/G | 0.00506878 | 0.0500869 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707363 | GAAGAAATGATTTAC[A/G]TTTTCCCGAGATGTA | 54442 |
rs79185719 | snp | A/G | 0.200182 | 0.244986 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690968 | CACCAGCAGTGAGCT[A/G]CCGAGGCCCTCGCGC | 54442 |
rs79322969 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687610 | TCACGGAGTGAGGTC[C/T]AAAGCCTCGCCAGGG | 54442 |
rs79422985 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704000 | TTTATTTCTGAGCTG[A/G]GTTTTTATAACCAAG | 54442 |
rs79479571 | snp | C/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683290 | CCTTTTTTTCCCTGG[C/T]GACTTGCATTTAGAG | 54442 |
rs79679889 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702627 | GACACACGGTCTCCC[A/G]TGGGACAGGTTCTCT | 54442 |
rs80041853 | snp | C/G | 0.030278 | 0.119257 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701407 | CCAGGGTCCCCAGTG[C/G]TCAGCAGGGGATTGC | 54442 |
rs80094947 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704162 | AATACCTGCTCTGAA[C/G]TGGGGCAGCTATGGC | 54442 |
rs111410528 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701082 | CGAACAGGGCTGTCC[C/G]CATGTGGCACCTGTG | 54442 |
rs111510225 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682326 | GTCGAGGCTGATGTC[C/G]GCTGCTCCCCATCAG | 54442 |
rs111523365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689760 | TTGGCTCACTGCAAC[A/G]GGGCTGTCAGGTTCA | 54442 |
rs111607468 | snp | A/G | 0.000247233 | 0.0111155 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707333 | AAGGATGTGAGGGAC[A/G]CAGTATTGACAGCTG | 54442 |
rs111675802 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686967 | GTGGGTGTCTGCGAC[A/G]CTGATGGACTTTGTT | 54442 |
rs111906906 | snp | A/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684778 | ACAAAAAAAAAAAAA[A/T]AAAAAAAAAATAAGC | 54442 |
rs111996924 | snp | G/T | 0.471292 | 0.116318 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693938 | ATGGCTGACAAAGGG[G/T]TTCTCTGGGGTTGTC | 54442 |
rs112121712 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707821 | GGGATCGCTGGTTTC[C/T]CTCGACCTCGCAGAG | 54442 |
rs112124562 | snp | G/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687781 | AGTCCCCAGGCATGG[G/T]CTTTAAAGCCTGGGG | 54442 |
rs112227668 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2685676 | GAGGAATCTGAGGAG[A/G]GGGGGAAGGGGTGTC | 54442 |
rs112357194 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684720 | CAGTGAGCCTAGTTA[A/G]CGCCACTGCAGTCCA | 54442 |
rs112383497 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693472 | GAGTGGCCAAGACAC[A/G]GCAGCGGCCTACCCC | 54442 |
rs112417580 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681953 | ACCATGTTGGCCAGC[A/G]TGGTCTCGATCTCCT | 54442 |
rs112466274 | snp | A/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688232 | ATAAATAAATAAATA[A/T]ATATATATATATATT | 54442 |
rs112503658 | in-del | -/AGAG | 0.0189856 | 0.0955633 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701645 | AACTGCGCAGGTCTT[-/AGAG]AGGCCAAAGTGTGAG | 54442 |
rs112574576 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687598 | TGCTCTGAAAGGTCA[C/T]GGAGTGAGGTCTAAA | 54442 |
rs112585635 | snp | G/T | 0.0763149 | 0.179815 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684743 | GCAGTCCAGCCTGGG[G/T]GAAAGAGCAAGACTC | 54442 |
rs112637150 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702167 | CATGCCATGCCACGG[C/T]GTGGGGTGCCGCCCC | 54442 |
rs112753749 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706978 | ACTGCTGAGGGACCC[A/G]CGGGCCGAGTTGCGC | 54442 |
rs112781903 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702171 | CCATGCCACGGCGTG[A/G]GGTGCCGCCCCGTGT | 54442 |
rs112990583 | snp | G/T | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701767 | CACAGAAGTGCCTGG[G/T]GGCCCAGGGTAGCCA | 54442 |
rs113007216 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692123 | GCACCCTGGAAAGGT[A/G]CCATGGCTCCGGCTG | 54442 |
rs113049391 | snp | C/T | 0.0748431 | 0.178382 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680976 | CAGAATGACTACGAA[C/T]AGGGGTCATTGTGCT | 54442 |
rs113190335 | in-del | -/G | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691511 | CTCCGGGAGAGGGCT[-/G]TGGGGGCAGCTGCAG | 54442 |
rs113201003 | in-del | -/C | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687742 | TGGTTCTTTTAGCAG[-/C]CCCCCTCCACGCCCC | 54442 |
rs113234631 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697252 | GAATGAAGACCACCC[A/T]TGAGGAAGCCCTGAG | 54442 |
rs113244545 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693724 | CAGGGCCTGAGAAGC[A/G]CATGGTGGGTTGTCT | 54442 |
rs113247669 | snp | A/C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681603 | ACATGAGCCACCGCG[A/C/T]CCGGCCTAAATTCTA | 54442 |
rs113359070 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2694095 | CTCTCTGTATGGGGG[G/T]GGGGCAGGGAGGAAC | 54442 |
rs113511306 | snp | A/C | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687146 | TGTGCTCACCTCTTT[A/C]TCAGGTGCCTCACCT | 54442 |
rs113696960 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2695571 | GCCCTAGGCCCCTGC[C/G]CTGCCCGCGAGGGCA | 54442 |
rs113759986 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693229 | CCATGCTGAGGGCAG[C/T]GGGCTATGGTGTGGG | 54442 |
rs113810303 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704316 | GGGCTGCGCAGGGCC[A/G]CATGGGCTGTGGGCC | 54442 |
rs113840324 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682212 | GTAGACGTTTGCTGG[C/T]ATGGCTCTTCCTTTG | 54442 |
rs113879488 | snp | A/G | 0.5 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702166 | CCATGCCATGCCACG[A/G]CGTGGGGTGCCGCCC | 54442 |
rs114141293 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690820 | AACCTCCCCGAGGTG[A/T]CCTTGCTGCCTTTGT | 54442 |
rs114244811 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684711 | AGGAGCTTGCAGTGA[A/G]CCTAGTTAGCGCCAC | 54442 |
rs114547732 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693597 | TTTCCGCCGATGGCC[A/G]TCCCCACCCTGCCCT | 54442 |
rs114575094 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692919 | GCAGGGATGCCTGAG[G/T]CTGTGGTTTGGGCAG | 54442 |
rs114618897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697758 | ACGTCTGCAGGAAGC[C/T]TGTTAGGTCGGGGCC | 54442 |
rs114711008 | snp | A/G | 0.0193772 | 0.0965046 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709241 | GGATCAGAGCTGCAC[A/G]GCCCATCCCTGCACC | 54442 |
rs114714195 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703145 | CTCGTTTGCTTTCAG[A/G]TTGGCCCTGTGGCCC | 54442 |
rs114733008 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691590 | AGAGGTCGTGGGGCT[C/G]AGAGAATTGAACCAC | 54442 |
rs114811733 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687867 | AGCCATCTCTCTCCC[A/G]GGACATGCTTGTTCT | 54442 |
rs114831978 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704133 | GAGAATGTGGCCCTA[C/T]TTCATTTTCCAAAAA | 54442 |
rs114937219 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687565 | CCCATTTGCTTACGG[A/G]TTGTGTGTGGCCGTT | 54442 |
rs114980339 | snp | A/G | 0.0379877 | 0.132479 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681602 | GACATGAGCCACCGC[A/G]CCCGGCCTAAATTCT | 54442 |
rs115100625 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693654 | GTTGCAGGGCTGGGG[C/T]TGCCTCGTGTGTCTG | 54442 |
rs115154633 | snp | A/T | 0.0410537 | 0.137264 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686965 | TAGTGGGTGTCTGCG[A/T]CGCTGATGGACTTTG | 54442 |
rs115398997 | snp | G/T | 0.00557542 | 0.0525036 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707958 | GTCAAGGCTTCTCAA[G/T]TTGTATTTTCCAGGC | 54442 |
rs115405593 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690241 | TGCGGAGTCTTCCTC[C/T]GTCTGCCAGGGCTGT | 54442 |
rs115519072 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701415 | CCCAGTGGTCAGCAG[A/G]GGATTGCAAGCAGGG | 54442 |
rs115559777 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705639 | CCTCCCAGGCCAGCC[A/G]TGTCCTGCAAGCCCC | 54442 |
rs115618920 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684662 | CCCAGCTACTAGGCA[G/T]TCTGAGGCAGGAGAA | 54442 |
rs115678449 | snp | A/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708568 | GCAGGTCAGAGGCTC[A/T]GACACTGTCTGGTTT | 54442 |
rs115694389 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702790 | GGGTCCTCTGTTCCC[C/T]GGGCCCAGCCTCTGC | 54442 |
rs116113618 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707805 | GCTCTGCCTCCCAGG[C/T]GGGATCGCTGGTTTC | 54442 |
rs116463433 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704307 | CCCCTGGCTGGGCTG[C/T]GCAGGGCCGCATGGG | 54442 |
rs116519598 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692645 | CACCACAAGTCCCCA[A/C]TTTGGTCCCCGGGAC | 54442 |
rs116615661 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693525 | GCCCAGTGCCAGCAC[A/G]CTCAGTGCCCTGCCG | 54442 |
rs116687480 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700952 | GCACCTCATCAGAAT[C/T]GTGCCAGAGCCTCCC | 54442 |
rs116943167 | snp | A/T | 0.0517044 | 0.152246 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686899 | GATGGCAGATGATGT[A/T]CTGTGTAGCCAGCAC | 54442 |
rs117061514 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683899 | GACCGTGATCAGGAA[A/G]TGAGAATCTGGAGTT | 54442 |
rs117171707 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697103 | TGTGCGGGACCCATG[C/T]GGGGCCGGGAAGCCT | 54442 |
rs117249074 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698777 | AGTTCCCCCTCCTGC[C/T]GGAGCTCCCTTGGTG | 54442 |
rs117359533 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687520 | ACCTGCCTGTTTTTG[C/T]AAGTAAAGTTTTACA | 54442 |
rs117578994 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708135 | CTCACGGGGAGCTGG[C/T]GTCTGTCAGTGCCTT | 54442 |
rs117598966 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699386 | AAGTCCAGGCTGCCG[C/T]GCAAGTTCAAGAGCC | 54442 |
rs117745015 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701388 | GGAGGTGGCCAGACC[A/G]GACCCAGGGTCCCCA | 54442 |
rs117780416 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706220 | TATTGGAGTCAGGCT[A/G]AGCAGCTCAGGGGAC | 54442 |
rs117900625 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701667 | CCAAAGTGTGAGCCT[C/T]GTCCAGCTGCTTTTT | 54442 |
rs117977913 | snp | C/T | 0.0399052 | 0.1355 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709465 | GTGAGCCATTGCGCG[C/T]GGCTCAAGTGATGTT | 54442 |
rs118076683 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692037 | AGCCTGAGCTCCAGG[A/G]ACTGAGACGAGCTGG | 54442 |
rs118149302 | snp | C/T | 0.0109894 | 0.0733071 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702364 | GCAGTTGGTCAGCAT[C/T]GGCTCCTCTTACAAC | 54442 |
rs137975835 | snp | A/G | 0.00496508 | 0.0495771 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698048 | CTGGTGTGAAGGAAG[A/G]GCTCCCCTTTACTCC | 54442 |
rs138151807 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687371 | GCCTCCAGACTTCTG[C/T]GGGTGGCTGGGAGGA | 54442 |
rs138204069 | snp | A/G | 0.107341 | 0.205301 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684462 | AATATGGTGATGCCC[A/G]GTCTCTACTAAAAAT | 54442 |
rs138257430 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707123 | ATGTGCCAGACACCC[C/T]GGTGAAGGTCCTGGG | 54442 |
rs138718767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706352 | GTGCCCGGCGAGGGC[A/G]TGGGCGTTGCTGCCC | 54442 |
rs138979709 | snp | C/T | 6.63515e-05 | 0.00575946 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699898 | GTCCACCATGTCCGA[C/T]GGCTGGAAGTTCGAG | 54442 |
rs139119909 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691013 | GTCTGGGCCTGGGCT[G/T]GCACCACGAGTAGCC | 54442 |
rs139128059 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708357 | TGCACGGGCTCTGCC[C/T]GACATGCCGTGGGAG | 54442 |
rs139140631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691684 | GGCGGGGGTGTGGAG[C/T]GGCTGGCAGGTTCTT | 54442 |
rs139276398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703456 | TGAGAGGCCAGAACC[A/G]GAAGGCTTTTAACTG | 54442 |
rs139279789 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699765 | CCTGGGCTGGGGCCA[C/G]AGGCAGCAGTGGGAC | 54442 |
rs139629027 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707963 | GGCTTCTCAATTTGT[A/G]TTTTCCAGGCAAGAG | 54442 |
rs139666192 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681930 | ATTTTCAGTGGAGAC[C/T]GGGCCTCACCATGTT | 54442 |
rs139666893 | snp | A/G | 0.229723 | 0.249176 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686112 | CACATCTAAGCTTCT[A/G]GGCTGTGACTGCCCC | 54442 |
rs139704972 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685445 | AAAAAAGAAAAAAGA[A/G]AAGGAGAAAACAATA | 54442 |
rs139783497 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682972 | TGCCCCGATCCCCTA[C/T]CCTGGGAGGGGAGGG | 54442 |
rs139873400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691970 | GGAAGGTTCCTGGGG[A/C]GTGCGGTTCCCACAC | 54442 |
rs139943939 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705092 | CCACCCGCACTGTCC[C/T]GACAGCCTGTCTTCT | 54442 |
rs140133666 | snp | A/G/T | 0.00166568 | 0.0288119 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702493 | GGTGAGTGCTGGGCC[A/G/T]GCCCTGGCCTGGGGC | 54442 |
rs140143341 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689831 | GAGGCACCCTCCACC[A/G]TGCCTGGCTAATTTG | 54442 |
rs140215165 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684924 | GCTTGGATGACAGAG[C/G]AAGACTCTGTCTCAA | 54442 |
rs140341939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697701 | TCGGCCCTCTCACCA[C/T]GGCCCCTCCGCCCAT | 54442 |
rs140623000 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689958 | TGGGATCACAGGCGT[A/G]AGCCACTGTGCCCAG | 54442 |
rs140663856 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683202 | CTTGCTGGCTCTGGA[A/G]ACAGAACCCTTGGCG | 54442 |
rs140772669 | in-del | -/C | 0.235854 | 0.249599 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701651 | CAGGTCTTAGAGAGG[-/C]CCAAAGTGTGAGCCT | 54442 |
rs140889784 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699048 | CGGGCATGTGACCTC[A/G]AGGCCACTGTGTGCC | 54442 |
rs141030305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697109 | GGACCCATGCGGGGC[C/T]GGGAAGCCTGTGTCT | 54442 |
rs141137037 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698166 | CCAGCTCCGTCTACC[A/C]GGCTCTCCCCAGGGT | 54442 |
rs141307822 | in-del | -/GA | 0.331874 | 0.236213 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700638 | AGCCCTCCCTGTCCT[-/GA]GAGTTTCCTCTGTCA | 54442 |
rs141343657 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685383 | AGTGGGCTGAGGTTG[C/T]GCCACTGCACTCCAG | 54442 |
rs141502691 | in-del | -/A | 0.0182019 | 0.0936463 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684735 | GCGCCACTGCAGTCC[-/A]AGCCTGGGTGAAAGA | 54442 |
rs141943108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706042 | CATCCCAGTAAACTT[C/G]GGAATCACCCTGGCC | 54442 |
rs141954139 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707756 | TCGTGGCCTCTGGTC[C/T]GACCACCAGGCCCTA | 54442 |
rs141975334 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703673 | CCTTTCCACCTCAGG[C/T]GACTGTCCTGGCCCA | 54442 |
rs142003699 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709082 | GGAATGCCACCCCGG[A/G]TCGCTCGGACCAAGG | 54442 |
rs142050785 | snp | A/C/T | 0.00438556 | 0.0466571 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684808 | CCAGGTGTGGTGGCG[A/C/T]GTGCCTGTAGTCCCA | 54442 |
rs142117942 | snp | C/T | 0.000646975 | 0.0179741 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699901 | CACCATGTCCGACGG[C/T]TGGAAGTTCGAGCAG | 54442 |
rs142154156 | snp | C/G | 0.00102859 | 0.0226548 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682805 | ACTCAGACAAGGTGA[C/G]GGCCTCACGGGCCAG | 54442 |
rs142327235 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691824 | AAGTCTCTTCCTAAC[A/T]GGATGCACGTGGGGT | 54442 |
rs142359102 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692557 | TGCCCTGCTCTGGCT[G/T]AGCCCAGGGCTCTTA | 54442 |
rs142394574 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689927 | GTAATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 54442 |
rs142561151 | in-del | -/TT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688246 | ATATATATATATATA[-/TT]TATTTATTTATTTAT | 54442 |
rs142731280 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706391 | GTTGGGCAGCCCTCA[C/T]GTGACACATGGAGAC | 54442 |
rs142887391 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697494 | GTGGCGTGGCCATGA[A/G]CAGGTTCCCAGCAGG | 54442 |
rs142996826 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692441 | AGCGGCCCCGGACTG[A/G]CTGGCTCCTCTCCAT | 54442 |
rs143141254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691259 | ACGCCACTGCCTCCC[C/T]GCCCTGGTGCGGATG | 54442 |
rs143211492 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703476 | GCTTTTAACTGGTGG[C/T]ATTAAACCAGGGACA | 54442 |
rs143365373 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705350 | TGGTGGGGCTGTTGC[C/T]GTGAGGCAGATGCCC | 54442 |
rs143587757 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705820 | CTGTCTAGAGTAGCC[C/T]GTGCTGCTCCCGGCC | 54442 |
rs143666262 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691100 | AGACCCTGCCTACAT[C/G]CTTGGAAGCGAGTCA | 54442 |
rs143731909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704018 | TTTTATAACCAAGCT[C/T]CCCTGGGCTCCTATC | 54442 |
rs143915922 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686959 | GGCCGTTAGTGGGTG[C/T]CTGCGACGCTGATGG | 54442 |
rs144028711 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684961 | AAAAAAATGCTTTAC[G/T]GTAGGAATCAATTCT | 54442 |
rs144134427 | snp | A/T | 0.16618 | 0.23553 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684772 | TCCATCACAAAAAAA[A/T]AAAAATAAAAAAAAA | 54442 |
rs144241694 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708087 | ATCCGTTAGCGCGAG[A/G]TAGCAGTGTCGCCTC | 54442 |
rs144382514 | snp | A/G | 4.94817e-05 | 0.00497377 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707351 | GTATTGACAGCTGAA[A/G]AAATGATTTACGTTT | 54442 |
rs144448373 | snp | A/G | 0.304937 | 0.243889 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686249 | CTTTCTAGACAGCCC[A/G]GTGTGAATTCTCACT | 54442 |
rs144519451 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698753 | CGCTGGCCACCTAGC[A/G]ACTTGCCCAGTTCCC | 54442 |
rs144726935 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682074 | TTGGGTCAATGATTT[A/C]ATCATATAATTTAAT | 54442 |
rs144849046 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698297 | GGCCCCATGAGGGCC[G/T]GTCGGGGAGACCCTG | 54442 |
rs144938570 | snp | A/C | 0.0149022 | 0.0850809 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699144 | CCCTTCTCACTGCTG[A/C]GTTTCCGTCCAGCCC | 54442 |
rs144941122 | snp | C/G | 0.46754 | 0.123192 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686685 | CCCGGCTTGAGGGTT[C/G]CAGATGTGGTGGCAT | 54442 |
rs145066470 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708886 | TGGTTTTTTTAATTT[A/G]AAGATATTAAGACTT | 54442 |
rs145199655 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690084 | GACAGCATGGATGGC[A/G]GAGAGCTGCAGCCGG | 54442 |
rs145281268 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683040 | CCTGAGTCGATTCAC[C/T]TTGGGGGTGTCTCTT | 54442 |
rs145464212 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697813 | CATGGGCCCTCATTG[C/T]AGGGGCAGGGGCAAG | 54442 |
rs145511603 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683275 | GTTGATATGGGCGGC[C/T]CTTTTTTTCCCTGGT | 54442 |
rs145782597 | snp | A/G | 0.00755907 | 0.0610114 | | | GRCh38.p7 | 16:2684112 | CTTTTATAAGTGTGG[A/G]TGTATGTTTTACTGT | 54442 |
rs145814843 | snp | C/G | 0.0252325 | 0.109451 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692051 | GGACTGAGACGAGCT[C/G]GGCAGAGCCTAGCCA | 54442 |
rs145833310 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703237 | CAAGATGGACAAATG[C/T]GTCCATCCAAGCAGA | 54442 |
rs145895260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706302 | CACTGCCCTCTCTCC[A/G]GTCAGTGCGGCATGG | 54442 |
rs145921685 | snp | C/T | 0.0119091 | 0.0762411 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681134 | GGGTGGCAGTCAGAA[C/T]ATGCGTAATATTCTC | 54442 |
rs145979392 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691911 | CTGCTGGCCCCTGAG[C/T]ACAGGGATGGGCTGG | 54442 |
rs145985918 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690522 | GTCTTAATTATGGCT[-/G]GTTTTAGAAAAAAAC | 54442 |
rs146065616 | snp | A/C | 0.0174175 | 0.0916809 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681841 | TGCCTCCCGGGTTCA[A/C]GCCATTCTCCTGCCG | 54442 |
rs146343345 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692967 | CCTGCTCCGTGGAGC[A/G]GGAAGCCCGGGTCTG | 54442 |
rs146344746 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707870 | TCTGCGTCGTCACTG[C/T]TTCCCGGCGCCATTC | 54442 |
rs146490693 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701212 | TAGCACTTCTGGGTG[G/T]ATTCCAAACCCATTG | 54442 |
rs146608871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685048 | ATCATCATCCATTTA[A/G]CCAGGTTTGATTTCC | 54442 |
rs146655864 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690662 | CACTGGCTTCCTGGC[C/T]GCCTCTCCTCATCCC | 54442 |
rs146809651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704522 | CTTGCTAGAAGGACT[C/T]GCAGAGCTCACTGAG | 54442 |
rs147261332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687196 | GCCACGAGTCAGTTC[C/T]ATAAATTCCTGAGAA | 54442 |
rs147299472 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699005 | TGTGACACAGTAGCA[G/T]CTCACTGTCTTGCAG | 54442 |
rs147336406 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696776 | CTCCTCCGAGTTCAC[A/G]CGGGGCGTGGAGTGA | 54442 |
rs147410660 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684634 | GCCAGGCGCGGTGGC[A/G]AGCACCTGTAGTCCC | 54442 |
rs147439881 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682958 | GCTCCTCCCCAGCTT[A/G]CCCCGATCCCCTACC | 54442 |
rs147531466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699505 | CTGCACGGTTGCTGC[A/G]TGCGGAGCAGACGTG | 54442 |
rs147547447 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703578 | CCTCTCCGAGTAGGC[C/G]TTTGGAGGTATGCCC | 54442 |
rs147563217 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683062 | GTGTCTCTTCCTCGC[C/T]CTCTTTGCTCTTTGG | 54442 |
rs147744733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692503 | TTCCCTCTGCAGCTG[G/T]TCTTCCACTTGCCAA | 54442 |
rs147759770 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709132 | CCAGCCCCACTGGCC[A/G]CGGCGGCTCACTCAG | 54442 |
rs147868059 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693496 | CTACCCCTGCCTGCC[C/T]GTCTTGAGGCCGAGC | 54442 |
rs148004840 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698971 | GGTGCAGGTGGGAGA[A/G]TCTGCGGTCCAGCCT | 54442 |
rs148239795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691450 | CAGCCTCTGGTGCCC[A/G]GCGGCTCAGCTGGGT | 54442 |
rs148272021 | snp | A/G | 0.000995768 | 0.0222911 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702415 | CGAGTTCCTCTGTGT[A/G]GTGTCCAAGGAGCTG | 54442 |
rs148353609 | snp | A/C | 0.0418186 | 0.138422 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680997 | TCATTGTGCTGGTAA[A/C]AGCCTCTATTACGAC | 54442 |
rs148549416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692276 | CAAGTTCCTGTTCTG[C/T]GTCCAGGAAGAATGA | 54442 |
rs148624502 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684792 | ATAAAAAAAAAATAA[A/G]CCAGGTGTGGTGGCG | 54442 |
rs148724877 | snp | A/G/T | 8.84134e-05 | 0.00664822 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707491 | TGGGTGGTGAGAGAC[A/G/T]GGCCCAGCTGTCCAA | 54442 |
rs148903527 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705677 | CCCGGGCCTGCCTGC[C/T]TGTGGGGGTGTCTGG | 54442 |
rs148937674 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686849 | ACCGTCTTTGAAGCC[A/G]CTTGGCAAGAGAAGT | 54442 |
rs148988809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683283 | GGGCGGCCCTTTTTT[C/T]CCCTGGTGACTTGCA | 54442 |
rs149166119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700847 | ACATTTGTGTCCCAC[C/T]GTCCACCCTGGACCC | 54442 |
rs149239244 | snp | A/C/G | 0.00716521 | 0.0594565 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698601 | TGAGCCCGCCCCCCC[A/C/G]ACCCAAGCTCAGCTC | 54442 |
rs149315554 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688471 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 54442 |
rs149379032 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682019 | GCTGGGATTACAGGC[C/G]TGAGCCACCAGGCCC | 54442 |
rs149489110 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703082 | GGGGCTCAGGCCCTT[C/G]TGTTTTCTGCGGGGC | 54442 |
rs149564820 | snp | C/T | 1.66921e-05 | 0.00288891 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702457 | GTACGGTACGGCCAG[C/T]GAGCCCAGCGAGAAG | 54442 |
rs149644884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707175 | ACCCTGGCCAGTGCC[A/G]CTGGGTTCCCGGGGC | 54442 |
rs149684952 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691996 | CACACAGGTGCGTCC[A/G]GGGGCTTCCTGGTCC | 54442 |
rs149703875 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683269 | GTGGGGGTTGATATG[A/G]GCGGCCCTTTTTTTC | 54442 |
rs149965647 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708482 | CGTGCAGGGCGGGCT[C/T]CAAGCGCTTTGCTTC | 54442 |
rs149981635 | snp | A/G/T | 0.000134353 | 0.00819512 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699945 | GCCAGCCTGGTGGCA[A/G/T]CCATGCTGCAGCTGA | 54442 |
rs150018216 | in-del | -/AAATAA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688223 | ATTAAATAAATAAAT[-/AAATAA]ATATATATATATATA | 54442 |
rs150034783 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696770 | GCCTGCCTCCTCCGA[A/G]TTCACGCGGGGCGTG | 54442 |
rs150112490 | snp | A/G | 0.000165686 | 0.00910031 | missense | KCTD5 | GRCh38.p7 | 16:2699827 | TCCTTGCAGGTGCCT[A/G]TGAAGCATGTGTACC | 54442 |
rs150417412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693727 | GGCCTGAGAAGCACA[C/T]GGTGGGTTGTCTTGG | 54442 |
rs150457497 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706889 | CAGGAGGGTCCGGGC[G/T]TCGGGGTGGGGGTGG | 54442 |
rs150470280 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689998 | GCCATTTTCAAGGCT[A/G]CTGGTTGCATTAGGG | 54442 |
rs150596756 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687642 | TGTGGCCGTGATGGG[A/G/T]GCGCCTGCTGCCTGG | 54442 |
rs150621142 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703954 | AGCAATCGTAGGGCT[C/G]TTTTCTAAATGGTTT | 54442 |
rs150794814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691534 | AGCTGCAGGCCCGGC[A/G]CGCCGAGTCCACGCA | 54442 |
rs150858249 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684346 | TTACTGTTCCTTAAG[A/G]CTTTGTTAAAAATTA | 54442 |
rs150934849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705832 | GCCCGTGCTGCTCCC[A/G]GCCTTGGGAGGGCGA | 54442 |
rs151063050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697544 | TGGAGGGAAAATGCC[A/G]GATCCAACCCCCAGC | 54442 |
rs151179019 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684895 | GTGAGTCAAGATCAC[A/G]CCACTGCACTCTAGC | 54442 |
rs151291061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689955 | TGCTGGGATCACAGG[C/T]GTAAGCCACTGTGCC | 54442 |
rs180795018 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683314 | TTTAGAGAGTTGGCG[C/G]TCCATCCTTTCCATC | 54442 |
rs180804159 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708230 | GTCACGGTGAAAATT[C/T]GGGATGTTTACAGAG | 54442 |
rs181088513 | snp | A/G/T | 0.000143046 | 0.00845592 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707448 | TTTTTCTAGAGATCT[A/G/T]GGTGTGAATCCTTTT | 54442 |
rs181183328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698943 | ACCTGTATGACGCAG[A/G]TGGGCAGGAAATGGT | 54442 |
rs181320131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702619 | ACTTCTTGGACACAC[A/G]GTCTCCCGTGGGACA | 54442 |
rs181405398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690689 | TCCCAGTCGTAGAGG[C/T]GTGAGCGGGCCGGGG | 54442 |
rs181471808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703260 | CAAGCAGAATCTGAC[C/T]TTGGCCTGGGCCAGC | 54442 |
rs181828478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688385 | CCTCCCAAGTAGCTG[A/G]GATTACAGGCACGAG | 54442 |
rs181834926 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692434 | GCAGAGAAGCGGCCC[C/T]GGACTGGCTGGCTCC | 54442 |
rs182015467 | snp | C/G | 0.000750751 | 0.0193601 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699227 | GCCCACTGGGGAGCA[C/G]CTCCATGCAGGCGGG | 54442 |
rs182199250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704210 | GGTGTCAGCAGTGCC[C/T]CAGGAGGCAGAGCTC | 54442 |
rs182258555 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687185 | TTAGACCTTAGGCCA[C/G]GAGTCAGTTCCATAA | 54442 |
rs182293616 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707635 | TCAGCCCGCTCGATC[A/C]TGAAGATCGTGTGAA | 54442 |
rs182437562 | snp | G/T | 0.000140569 | 0.00838242 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682514 | AAGCCGGACGCTTCC[G/T]GTGGAAGGGAGCTGT | 54442 |
rs182500299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684580 | ACCATCCTGGCTAAC[A/C]TGATGAAACTCTGTC | 54442 |
rs182511795 | snp | C/T | 0.00478085 | 0.0486577 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709301 | CAGCAGATAGCATAC[C/T]CCCATCCCGGGAGAC | 54442 |
rs182622499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699691 | ATGTGCTCAGGATTG[C/T]TTTGGGCCTCGTGCC | 54442 |
rs183080260 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691621 | GTGGGAGGAGTGTAC[G/T]GTGGCGGGGGCCCCA | 54442 |
rs183081291 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680606 | ACTTGACATGAGCCT[A/T]TGTTGACTCACTGGG | 54442 |
rs183088896 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705564 | GGTCAGGACCAGTGC[A/G]GCAGACAGCAGACCC | 54442 |
rs183101293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701753 | TTTCCCTTTAAAAGC[A/G]CAGAAGTGCCTGGTG | 54442 |
rs183211848 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704941 | GGACCAGCCCCGGAT[C/T]GCAAGATGCAGCCGC | 54442 |
rs183364353 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691453 | CCTCTGGTGCCCGGC[A/G]GCTCAGCTGGGTTCT | 54442 |
rs183463215 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692359 | TGGGACAGTGCAGAG[C/G]AGACTGTGGGGGCAG | 54442 |
rs183960699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702644 | GGGACAGGTTCTCTC[A/G]ACACAGGCTCCCAGT | 54442 |
rs184095431 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681225 | AAAACAAATAATACA[A/G]TGGTATTAGGATATA | 54442 |
rs184102691 | snp | C/T | 0.000579869 | 0.0170176 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707274 | CAGCCCAAGTCCTCA[C/T]TTTATGCATTTGGTG | 54442 |
rs184234230 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686964 | TTAGTGGGTGTCTGC[A/G]ACGCTGATGGACTTT | 54442 |
rs184336954 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707536 | AAGTTGGGGGAGCAC[A/G]GCGGCCGGGTGGGCG | 54442 |
rs184419979 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682000 | CGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTACA | 54442 |
rs184440556 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702237 | CATTTCCTGAAGCGT[C/T]GGCAGTCTTTGCTGT | 54442 |
rs184593044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687338 | ACCTGACATGGGCCC[A/G]CGGTCTTCGGCATTC | 54442 |
rs184872901 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697819 | CCCTCATTGCAGGGG[A/C]AGGGGCAAGGGCAGG | 54442 |
rs185020163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702137 | TCAGGGTCCTCACAG[A/G]GGAAGAGCTCGCCCC | 54442 |
rs185168261 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683484 | TGCTTTCTAATTGGC[C/T]TAGTTTTCCCACTGT | 54442 |
rs185178255 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709043 | GAATGCGCGTAGTAG[C/T]TGTTTATGGTCTTAA | 54442 |
rs185250267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693632 | CCCTCCTGCCTTCAT[C/T]CTTCCAGTTGCAGGG | 54442 |
rs185321261 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2689912 | AACTCCTCACCTCAG[A/G]TAATCCGCCTGCCTT | 54442 |
rs185402569 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680986 | ACGAATAGGGGTCAT[C/T]GTGCTGGTAAAAGCC | 54442 |
rs185531315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706112 | TCCTCCGAGGCACTG[A/G]AGAGTGAGTGGGAGC | 54442 |
rs185720078 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703801 | GCAGGCCCTGGTGTG[C/G]GACAGCCGGGGTGGA | 54442 |
rs185811664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688136 | CCCGCCCCGTACCTG[A/G]TGCCAGGTCAGTGCA | 54442 |
rs185985420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704490 | CACACCTGCTTCCCA[C/T]GCCAGTCCCTCAAGA | 54442 |
rs186256452 | snp | C/T | 0.00023488 | 0.0108344 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699285 | AGGACCACAGCTGCC[C/T]GGAGGGGCACAGCAA | 54442 |
rs186333448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690979 | AGCTGCCGAGGCCCT[C/T]GCGCCTGGGCTGGGC | 54442 |
rs186565543 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687217 | TTCCTGAGAAAAGGA[C/G]TCGACTCTGGTGATG | 54442 |
rs186691944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691891 | CTGGGTATTTTGCAC[C/T]CAGGCTGCTGGCCCC | 54442 |
rs186708426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698460 | CGGCTCGCCACAGAC[A/G]CACCTCTCACAGCTG | 54442 |
rs186772243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699098 | TGGCATGAGTCACCA[C/T]CTTAAGGTCAGGGAC | 54442 |
rs186840601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691547 | GCGCGCCGAGTCCAC[A/G]CAGCCTGGGTAGGTC | 54442 |
rs186999626 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684625 | AAAAAATGAGCCAGG[C/T]GCGGTGGCGAGCACC | 54442 |
rs187082411 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705463 | CAAGAGCCCCTCCTG[C/G]GGGCTGGGCAGGGAG | 54442 |
rs187373436 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708155 | GTCAGTGCCTTGTCA[C/T]GCCTGGCATAGAGGT | 54442 |
rs187421807 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705616 | GCGGCATCCCTGATG[C/T]GCTTAAGCCTCCCAG | 54442 |
rs187647538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701857 | CCTGCCTGGTGACCC[A/G]GAGGGAGGCAGGTTG | 54442 |
rs187749662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706683 | GGGAGGGCAGGGGGC[C/T]GAGGGGCCGTGGGCT | 54442 |
rs187752013 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700095 | GAGCCTTGGGAGTTC[A/G]GGTGGGGTGGGCAGA | 54442 |
rs187908959 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692629 | GCAGGCCCGGAAAAC[A/G]CACCACAAGTCCCCA | 54442 |
rs188026121 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681156 | AATATTCTCTACCTG[A/G]TCTGTAGCTGTAACT | 54442 |
rs188121195 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689918 | TCACCTCAGGTAATC[C/T]GCCTGCCTTGGCCTC | 54442 |
rs188261553 | snp | C/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680873 | CTCATTTCTTCCATA[C/T]GAAGAAACACCAAAC | 54442 |
rs188468097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698242 | CCCCAAAGGATGGCT[C/T]TGAGGAAGTTGGGCA | 54442 |
rs188490065 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681381 | GCAGTGGCCTGATCT[C/T]GGCTAACTGCAACCT | 54442 |
rs188496077 | snp | A/G | 0.000624305 | 0.0176568 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707429 | AGAAACCTGCTTTTG[A/G]TCATTTTTCTAGAGA | 54442 |
rs188689683 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687060 | TATTCTGGACCTCTG[C/G/T]GATGGTCCCTGCGGT | 54442 |
rs188878128 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697687 | GTTCAGTCCACACAT[C/T]GGCCCTCTCACCACG | 54442 |
rs189131543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703030 | AGAGTAGGCCCTTTG[C/T]GGCACCCAGCCTGGC | 54442 |
rs189273223 | snp | G/T | 0.01964 | 0.0971301 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702499 | TGCTGGGCCGGCCCT[G/T]GCCTGGGGCAGTCTT | 54442 |
rs189282406 | snp | A/G | 0.00795532 | 0.062565 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708220 | GAAGGTCTGCGTCAC[A/G]GTGAAAATTCGGGAT | 54442 |
rs189520418 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688320 | TGGTGGGGTGATCTC[A/G/T]GCTCACTGCAACCTC | 54442 |
rs189645409 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698929 | GCCTCAGTCTACCTA[A/C]CTGTATGACGCAGGT | 54442 |
rs189810821 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682114 | CTTTTTTTCCCCCCA[A/T]ATATTTGTGCTTTAG | 54442 |
rs189838873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699658 | CAGCTGTTCGGGCCG[C/T]GTGTTTTGCTTTTGT | 54442 |
rs190073801 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707567 | CTGCCTCTTGGGGGG[A/G]CCTCGCTCTGTTTTT | 54442 |
rs190334375 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709097 | GTCGCTCGGACCAAG[A/G]TGCTGCCCCTCCAAG | 54442 |
rs190348320 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699145 | CCTTCTCACTGCTGC[A/G]TTTCCGTCCAGCCCC | 54442 |
rs190410146 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687815 | AACCTGCCTGCCTGG[C/T]GCCATGGGAGGGGTC | 54442 |
rs190766600 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680593 | CAGTTATTTTCAAAC[A/T]TGACATGAGCCTATG | 54442 |
rs190770954 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705464 | AAGAGCCCCTCCTGG[A/G]GGCTGGGCAGGGAGT | 54442 |
rs190981436 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691607 | GAGAATTGAACCACG[A/T]GGGAGGAGTGTACTG | 54442 |
rs191131200 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682983 | CCTACCCTGGGAGGG[G/T]AGGGTGAGGATGGCG | 54442 |
rs191184260 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700273 | GCAATCCCCGTCCCC[C/G]ACAGCTCACTCCATC | 54442 |
rs191255606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692321 | GGAGGGTGAGCATGA[C/T]GAAGAGAAGCTTTAC | 54442 |
rs191272439 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681208 | AATTAAAAGAACTCA[A/T]GAAAACAAATAATAC | 54442 |
rs191418661 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687179 | AGCCCTTTAGACCTT[A/G]GGCCACGAGTCAGTT | 54442 |
rs191541328 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684771 | CTCCATCACAAAAAA[A/T]AAAAAATAAAAAAAA | 54442 |
rs191701775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687235 | GACTCTGGTGATGAA[A/G]TGGAACGTTTCTGAT | 54442 |
rs191997028 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691168 | GTCCTGGTTTAAGAC[C/T]CTGGCACTTCCTATG | 54442 |
rs192024975 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703990 | TTAGAAGTTTTTTAT[G/T]TCTGAGCTGAGTTTT | 54442 |
rs192143305 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702017 | GCCGCCCTCCACTCT[C/T]CTCCCGCTGCCCCCC | 54442 |
rs192547269 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697688 | TTCAGTCCACACATC[A/G]GCCCTCTCACCACGG | 54442 |
rs192712467 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706973 | ACTGGACTGCTGAGG[A/G]ACCCGCGGGCCGAGT | 54442 |
rs192839960 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693586 | CTGCTGTGCAGTTTC[C/T]GCCGATGGCCGTCCC | 54442 |
rs192855194 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687889 | GCTTGTTCTCCCTGG[C/G]CGTCAACTCGGCAGT | 54442 |
rs193101460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705821 | TGTCTAGAGTAGCCC[A/G]TGCTGCTCCCGGCCT | 54442 |
rs193219700 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702182 | CGTGGGGTGCCGCCC[C/G]GTGTGCTCGTGCAGG | 54442 |
rs199512646 | snp | C/T | 0.00199808 | 0.0315444 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682737 | TCGGCAGACCCTGTG[C/T]CGGGACCCGAAATCC | 54442 |
rs199627311 | snp | A/G | 0.00299557 | 0.0385851 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680825 | GGTGAGCAACTGAAC[A/G]AGCCTACGTGTGTAC | 54442 |
rs199653124 | in-del | -/TTTCTT | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681743 | CTTTATTACAAAAAC[-/TTTCTT]TTTTTTTTTTTGAGA | 54442 |
rs199688192 | in-del | -/ATAAATAAATAT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688221 | TTATTAAATAAATAA[-/ATAAATAAATAT]ATATATATATATATT | 54442 |
rs199800740 | snp | C/G/T | 0.00478371 | 0.0486721 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682532 | GGAAGGGAGCTGTTG[C/G/T]GGGGCTTGCTGGGAT | 54442 |
rs199853022 | snp | A/G | | | missense | KCTD5 | GRCh38.p7 | 16:2697938 | GAATTTTACAATATC[A/G]CCTCATTAATAAAAC | 54442 |
rs200033685 | snp | C/T | 0.00059754 | 0.0172746 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707269 | CTCCTCAGCCCAAGT[C/T]CTCATTTTATGCATT | 54442 |
rs200063997 | in-del | -/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684778 | ACAAAAAAAAAAAAA[-/T]AAAAAAAAAATAAGC | 54442 |
rs200090619 | in-del | -/TATATATATT | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688238 | AAATAAATATATATA[-/TATATATATT]TATTTATTTATTTAT | 54442 |
rs200209977 | snp | C/T | 1.66054e-05 | 0.00288139 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702347 | TCAGGCTATGTCTCC[C/T]TGCAGTTGGTCAGCA | 54442 |
rs200225165 | in-del | -/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2689684 | TGCCGTTTTCTTTTC[-/T]TTTTTTTTTTTTGAG | 54442 |
rs200585517 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688251 | TATATATATATTTAT[A/T]TATTTATTTATTTAT | 54442 |
rs200814719 | snp | C/G | 0.00299557 | 0.0385851 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682456 | GCGGGCGCTCTACCA[C/G]GGCGGACCTGTGGGC | 54442 |
rs200832017 | snp | C/G/T | 2.89498e-05 | 0.00380448 | missense | KCTD5 | GRCh38.p7 | 16:2682619 | GGCTGGGGGGCGGCC[C/G/T]GTGCCGCCGCTGCAG | 54442 |
rs200900245 | snp | C/T | 0.00113216 | 0.0237655 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702309 | AGCCTGGCTGGGTCT[C/T]TCAGGCTTCACTGGG | 54442 |
rs200979195 | snp | A/C/T | 0.00153231 | 0.0276399 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702307 | TCAGCCTGGCTGGGT[A/C/T]TCTCAGGCTTCACTG | 54442 |
rs201107320 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684903 | AGATCACGCCACTGC[A/C]CTCTAGCTTGGATGA | 54442 |
rs201349674 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702353 | TATGTCTCCTTGCAG[C/T]TGGTCAGCATCGGCT | 54442 |
rs201376163 | snp | C/G | 5.07567e-05 | 0.00503744 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702510 | CCCTGGCCTGGGGCA[C/G]TCTTGGGTGGGGAAG | 54442 |
rs201414149 | snp | A/G | 4.94499e-05 | 0.00497217 | missense | KCTD5 | GRCh38.p7 | 16:2707311 | AGATTTTGCAAGAAC[A/G]AGGCTCAAGGATGTG | 54442 |
rs201544210 | snp | A/C/T | 7.26583e-05 | 0.006027 | missense, synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682573 | AATCACTGCGAGCTC[A/C/T]TGTCGCCGGCCCGGG | 54442 |
rs201718226 | snp | A/G | 3.99576e-05 | 0.00446959 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682506 | GCTATTAAAAGCCGG[A/G]CGCTTCCGGTGGAAG | 54442 |
rs201776425 | snp | A/T | 0.000399281 | 0.0141238 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697943 | TTACAATATCACCTC[A/T]TTAATAAAACTTGTA | 54442 |
rs201857795 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2694216 | GCCCAGCGTCCTCTT[C/T]CCGGGAGCTGGCCCT | 54442 |
rs201883396 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687741 | TTGGTTCTTTTAGCA[-/G]CCCCCCTCCACGCCC | 54442 |
rs201954966 | snp | C/G/T | 0.00212407 | 0.03252 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707370 | TGATTTACGTTTTCC[C/G/T]GAGATGTAATGAACT | 54442 |
rs202098208 | snp | C/T | 4.97781e-05 | 0.00498864 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702388 | TTACAACTATGGGAA[C/T]GAAGACCAAGCCGAG | 54442 |
rs367644972 | snp | C/T | 8.32979e-05 | 0.00645306 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702310 | GCCTGGCTGGGTCTC[C/T]CAGGCTTCACTGGGC | 54442 |
rs367687515 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706503 | TGGTCTCTGGAGCTG[C/T]CATGGCTCATTTTGG | 54442 |
rs367794885 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696767 | TCTGCCTGCCTCCTC[A/C]GAGTTCACGCGGGGC | 54442 |
rs367905860 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693828 | GCTACACGAGCTGGT[A/C]TCCCCCACCTTTTGC | 54442 |
rs367970490 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701702 | TGGTCATCTGCTGCT[G/T]TCATGCTTATTGTGA | 54442 |
rs368009497 | snp | C/G | 0.0905309 | 0.192535 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686759 | AGTGTACTGGGTGTT[C/G]GCAAGACCTCGGGGG | 54442 |
rs368106074 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690053 | CCCCCACGTTGCCCC[C/G/T]GGTGCTTTGCTGGGT | 54442 |
rs368109375 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706977 | GACTGCTGAGGGACC[C/T]GCGGGCCGAGTTGCG | 54442 |
rs368186661 | snp | A/G | 5.39069e-05 | 0.00519139 | missense | KCTD5 | GRCh38.p7 | 16:2682628 | GCGGCCTGTGCCGCC[A/G]CTGCAGCGCTGGGCT | 54442 |
rs368520189 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688028 | GCCTTATGACTTGGG[C/G]TGATTTCGTGCCCCT | 54442 |
rs368559049 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682106 | AATCTGTTCTTTTTT[C/T]CCCCCCAAATATTTG | 54442 |
rs368586728 | snp | A/G | 0.00018138 | 0.00952141 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682519 | GGACGCTTCCGGTGG[A/G]AGGGAGCTGTTGCGG | 54442 |
rs368678897 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699954 | GTGGCAGCCATGCTG[C/T]AGCTGAACTTGTGCT | 54442 |
rs368679633 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684118 | TAAGTGTGGGTGTAT[A/G]TTTTACTGTTTGGTT | 54442 |
rs368718871 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684773 | CCATCACAAAAAAAA[A/T]AAAATAAAAAAAAAA | 54442 |
rs368735694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699057 | GACCTCGAGGCCACT[A/G]TGTGCCTTTGTCACT | 54442 |
rs368889018 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682803 | GGACTCAGACAAGGT[A/G]AGGGCCTCACGGGCC | 54442 |
rs368940704 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686883 | GATCACGTCTAGTGG[A/T]GATGGCAGATGATGT | 54442 |
rs368987044 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707657 | TCGTGTGAAGGAAGC[A/G]TTCTTGGTGCTACAC | 54442 |
rs369014865 | in-del | -/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701468 | AGGGGCTCCGGGGGG[-/G]CATGGCCGTGAGTGC | 54442 |
rs369030658 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704121 | CCCTTTGTGGTTGAG[A/T]ATGTGGCCCTATTTC | 54442 |
rs369201446 | snp | A/G | 1.64814e-05 | 0.00287061 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707330 | CTCAAGGATGTGAGG[A/G]ACACAGTATTGACAG | 54442 |
rs369415507 | in-del | -/AGAG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701647 | CTGCGCAGGTCTTAG[-/AGAG]GCCAAAGTGTGAGCC | 54442 |
rs369480617 | snp | C/G/T | 3.35673e-05 | 0.00409668 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698004 | ACATCGCAGGTGAGA[C/G/T]AAATGACTGAGGCTG | 54442 |
rs369640060 | snp | C/G | 6.77587e-05 | 0.0058202 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698017 | GACAAATGACTGAGG[C/G]TGGAAGCTTGTATGG | 54442 |
rs369760567 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682906 | CGGGAGCGGGCGACT[C/G]TCCTCGGGCTTCGAG | 54442 |
rs369763741 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697528 | CGTCGGCCTCCAGGC[G/T]TGGAGGGAAAATGCC | 54442 |
rs369879413 | snp | A/G | 3.47264e-05 | 0.00416678 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682829 | GGGCCAGCCCGGAGG[A/G]TCCTGGCCTTCCCGG | 54442 |
rs369894980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684350 | TGTTCCTTAAGACTT[A/T]GTTAAAAATTATGGG | 54442 |
rs369972843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704688 | GTTGGGGCTCCATTG[C/T]GTAGCCATGCTCGAT | 54442 |
rs369992391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696867 | GTCTCTTTGGCAGGG[A/C]ATGTCTTTCACATGT | 54442 |
rs370061716 | snp | A/C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684962 | AAAAAATGCTTTACT[A/C/G]TAGGAATCAATTCTT | 54442 |
rs370248607 | snp | C/T | 0.000317824 | 0.012602 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699935 | AGGGGCCCTGGCCAG[C/T]CTGGTGGCAGCCATG | 54442 |
rs370286413 | snp | C/T | 1.65392e-05 | 0.00287564 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707362 | TGAAGAAATGATTTA[C/T]GTTTTCCCGAGATGT | 54442 |
rs370349544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693546 | TGCCCTGCCGGCTCC[C/T]TGGACCTGTCTGTGT | 54442 |
rs370391310 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687337 | CACCTGACATGGGCC[C/T]GCGGTCTTCGGCATT | 54442 |
rs370490796 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709310 | GCATACCCCCATCCC[A/G]GGAGACCGGAGACCA | 54442 |
rs370596936 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705270 | GTGTGTCTGTCCCTG[C/T]CTGTAGTTGACGAGA | 54442 |
rs370628104 | snp | A/G | 5.02618e-05 | 0.00501282 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699939 | GCCCTGGCCAGCCTG[A/G]TGGCAGCCATGCTGC | 54442 |
rs370677337 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687924 | CATGGACTGCAGAAT[C/G]TCTAGAACATTCTGG | 54442 |
rs370677522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705664 | AGCCCCTCAGCCACC[C/T]GGGCCTGCCTGCCTG | 54442 |
rs370766760 | in-del | -/G | 0.000554022 | 0.0166344 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682533 | GAAGGGAGCTGTTGC[-/G]GGGCTTGCTGGGATC | 54442 |
rs370829616 | snp | A/C | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709109 | AAGGTGCTGCCCCTC[A/C]AAGCCGCCCAGCCCC | 54442 |
rs370951671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701759 | TTTAAAAGCACAGAA[A/G]TGCCTGGTGGCCCAG | 54442 |
rs370977047 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692960 | GGGCCTGCCTGCTCC[A/G]TGGAGCGGGAAGCCC | 54442 |
rs371079559 | snp | A/G | 0.000116565 | 0.0076334 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707371 | GATTTACGTTTTCCC[A/G]AGATGTAATGAACTG | 54442 |
rs371110318 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705890 | AGGGTGTCTCCTGCC[C/T]TCATCAGGAGGGAGC | 54442 |
rs371152268 | in-del | -/TAAATAAA | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688210 | CTTGGTTTTTATTAT[-/TAAATAAA]TAAATAAATAAATAT | 54442 |
rs371345939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684836 | CCAGCTACTCTGGAG[C/G]CTGAGGCAGAAGAAT | 54442 |
rs371740693 | snp | G/T | 8.32272e-05 | 0.00645032 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702323 | TCTCAGGCTTCACTG[G/T]GCTGCGTCTCAGGCT | 54442 |
rs371839085 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691631 | TGTACTGTGGCGGGG[A/G]CCCCATAGGAAGCCC | 54442 |
rs372010674 | snp | A/G | 1.66918e-05 | 0.00288888 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2697994 | AGACAGCAAAACATC[A/G]CAGGTGAGACAAATG | 54442 |
rs372046007 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701887 | GGAGTGGCCTAAGGG[C/T]GTGGCCAGCAGGCTG | 54442 |
rs372089756 | snp | C/T | 1.70726e-05 | 0.00292164 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682710 | CGTCGGCGGCACCTA[C/T]TTCCTCACCACTCGG | 54442 |
rs372221749 | snp | A/G | 3.31879e-05 | 0.00407343 | missense | KCTD5 | GRCh38.p7 | 16:2702360 | CCTTGCAGTTGGTCA[A/G]CATCGGCTCCTCTTA | 54442 |
rs372229228 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699129 | CCAGGACCTCTGAAC[C/T]CCTTCTCACTGCTGC | 54442 |
rs372280699 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706979 | CTGCTGAGGGACCCG[C/T]GGGCCGAGTTGCGCT | 54442 |
rs372595787 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692057 | AGACGAGCTGGGCAG[A/G]GCCTAGCCACTGTGG | 54442 |
rs372638703 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692715 | AAGGTGGGGCCTTAC[C/T]GGGGACCTACCCCCT | 54442 |
rs372768771 | snp | C/G | 0.000435183 | 0.0147446 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699936 | GGGGCCCTGGCCAGC[C/G]TGGTGGCAGCCATGC | 54442 |
rs372773152 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2686947 | GCCTCAGTTTGAGGC[C/T]GTTAGTGGGTGTCTG | 54442 |
rs372990565 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704931 | TGGTGGGACAGGACC[A/G]GCCCCGGATCGCAAG | 54442 |
rs373039549 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681882 | AGTAGCTTGGATTAC[C/T]GGCGCCCACCACCGC | 54442 |
rs373142824 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708832 | TGCTGGCCGCTTAGC[A/G]TTGTTTGATTTTTGA | 54442 |
rs373220103 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2697573 | GCATACCATGGCCTC[A/G]GCGTAGACATACGCT | 54442 |
rs373313436 | snp | C/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708584 | GACACTGTCTGGTTT[C/G]CAATGCTTCTGGAGA | 54442 |
rs373332133 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687356 | GTCTTCGGCATTCTC[A/G/T]CCTCCAGACTTCTGC | 54442 |
rs373383340 | snp | A/C | 1.67206e-05 | 0.00289137 | missense | KCTD5 | GRCh38.p7 | 16:2702471 | GCGAGCCCAGCGAGA[A/C]GGCCAAGGTGAGTGC | 54442 |
rs373446553 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2707206 | TCCCCGAGCTAACCC[C/T]AGGCCTGTGGGCTCT | 54442 |
rs373563522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700175 | TTCTTCCCAGCGCTG[C/T]GCTTTCTTCGCATCA | 54442 |
rs373840960 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704351 | TCGCTGGTGTCCCTG[C/T]AGCATGTGTGGCCTG | 54442 |
rs373881306 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681773 | TTGAGACAGACTCTC[A/G]CCCTATCACCAGGCT | 54442 |
rs373956716 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691489 | CACGCAGGGCTCTGC[A/C]GTGTCACTCCGGGAG | 54442 |
rs374081806 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2696775 | CCTCCTCCGAGTTCA[C/T]GCGGGGCGTGGAGTG | 54442 |
rs374089614 | snp | A/G | 3.32408e-05 | 0.00407668 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699781 | AGGCAGCAGTGGGAC[A/G]TGGGTGGCCCGCCCT | 54442 |
rs374101984 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701635 | CCGTTGGTCCAACTG[C/T]GCAGGTCTTAGAGAG | 54442 |
rs374150295 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684428 | AGGCAGGTGGATCTC[A/G]TTCAAAACCAACCGG | 54442 |
rs374183656 | snp | A/C/G | 6.76732e-05 | 0.00581658 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698016 | AGACAAATGACTGAG[A/C/G]CTGGAAGCTTGTATG | 54442 |
rs374230094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704405 | ACTTCAGTCAGCGGC[A/G]GCGGGAGAGCCTGGG | 54442 |
rs374248087 | snp | A/G | 6.19982e-05 | 0.00556734 | missense | KCTD5 | GRCh38.p7 | 16:2682609 | ATCGGGGCGGGGCTG[A/G]GGGGCGGCCTGTGCC | 54442 |
rs374376687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688009 | ATCTGCCCACCTCTG[A/G]CCTGCCTTATGACTT | 54442 |
rs374380500 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705769 | GATGGCCTAGGGAGA[A/C]AGTGTGTCCAGAAAA | 54442 |
rs374467037 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2684251 | GGGTTCTTTGAGGCA[A/G]TGGTTGTCTATTCAG | 54442 |
rs374503468 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683351 | ACGCAGCACCCACTC[A/G]GCACCTCTTAGAAGA | 54442 |
rs374578946 | snp | A/G | 0.00201013 | 0.031639 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682517 | CCGGACGCTTCCGGT[A/G]GAAGGGAGCTGTTGC | 54442 |
rs374992478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701276 | CGACCTGCTTGGCAC[A/G]CTTCATCCCTTGGGG | 54442 |
rs375198394 | snp | G/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681484 | TCTGGCTAATTTTTT[G/T]TATTTTTGGTAGAGA | 54442 |
rs375210509 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706842 | TGGCCAGGCTGAGGT[A/G]CAGGGCCGAGGGCTT | 54442 |
rs375266589 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698376 | CAGCATGGCTGGAGG[A/G]AGACAGCAGATGGGT | 54442 |
rs375487247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693017 | GCGAACCCCAGGGCT[A/G]CAGCCCCAGGCAGCC | 54442 |
rs375502620 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692389 | GCTCCTCTCTGTAGG[C/T]AGGTCGGCTCATTCA | 54442 |
rs375530628 | snp | A/G | 3.33778e-05 | 0.00408507 | missense | KCTD5 | GRCh38.p7 | 16:2702458 | TACGGTACGGCCAGC[A/G]AGCCCAGCGAGAAGG | 54442 |
rs375630698 | snp | A/G | 0.000437904 | 0.0147905 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707395 | TGAACTGCCATGTCC[A/G]GGAAGCTTGGCTGTG | 54442 |
rs375925343 | snp | C/T | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709182 | AGTCGATGGCCAGGG[C/T]GGAGCTGGGCCATCC | 54442 |
rs376014417 | snp | C/G | 0.00031825 | 0.0126105 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699938 | GGCCCTGGCCAGCCT[C/G]GTGGCAGCCATGCTG | 54442 |
rs376100605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705410 | GACTGGAGGGTGCCC[A/G]TGCCAGGCCAGGCTG | 54442 |
rs376104362 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687450 | CCTTCAGTGGCTGTC[A/G]TCCAGCAGGGCAGTG | 54442 |
rs376141066 | snp | C/T | 4.98434e-05 | 0.00499192 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699791 | GGGACATGGGTGGCC[C/T]GCCCTTACCTGTGCC | 54442 |
rs376173146 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705035 | TGGCGTGGCCTCACT[A/G]GAAGGTCACCGGGCG | 54442 |
rs376188069 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707111 | TGGGGCCTGGAGATG[G/T]GCCAGACACCCCGGT | 54442 |
rs376226028 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692771 | TGCTGCCATACATGG[C/T]GCCTGGGCTCGGCCC | 54442 |
rs376275154 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703796 | CTGGGGCAGGCCCTG[C/G]TGTGGGACAGCCGGG | 54442 |
rs376287454 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690878 | ATTTTGTATGATTTT[A/G]TGTTTCCCATTTTCC | 54442 |
rs376360208 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704026 | CCAAGCTCCCCTGGG[C/T]TCCTATCCCTCAGGT | 54442 |
rs376612057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697333 | CCTAAGTGCGGCACA[C/T]TACGGATGGCAGTCT | 54442 |
rs376625532 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698035 | GAAGCTTGTATGGCT[A/G]GTGTGAAGGAAGGGC | 54442 |
rs376746520 | snp | A/G | 3.32287e-05 | 0.00407593 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702341 | TGCGTCTCAGGCTAT[A/G]TCTCCTTGCAGTTGG | 54442 |
rs376753316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700750 | CTCTGAATGAAAGCT[A/C]CCTTTTCCTTGGAGT | 54442 |
rs376794130 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2690663 | ACTGGCTTCCTGGCC[A/G]CCTCTCCTCATCCCA | 54442 |
rs376822951 | snp | C/T | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707535 | CAAGTTGGGGGAGCA[C/T]GGCGGCCGGGTGGGC | 54442 |
rs376857381 | in-del | -/T | 0.0310518 | 0.120672 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681015 | CCTCTATTACGACTG[-/T]TAAGTTGGATGTTGG | 54442 |
rs376997633 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687089 | GTGCTGGGGGCTCCC[C/T]GCTCCTTCCCCACTG | 54442 |
rs377068877 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701056 | AAGCCGTGTCAGCAG[C/T]TCGGGGTCCGCGAAC | 54442 |
rs377155480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693361 | CTGGGCCAGCTGTGG[C/T]CAGACTGAGGTCAGG | 54442 |
rs377197615 | snp | C/G | 0.00025277 | 0.0112393 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702496 | GAGTGCTGGGCCGGC[C/G]CTGGCCTGGGGCAGT | 54442 |
rs377215953 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687015 | ATGTGGCTCTGAGCA[C/T]GATCTTCGCTCTGAC | 54442 |
rs377217225 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2704606 | TCAGATCAGCAAGGG[C/T]GGGCACCTGGGCAGA | 54442 |
rs377372799 | snp | C/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682386 | CTCCCGCCGGAAGCG[C/G]GCCCAGCCTCCTGCT | 54442 |
rs377416612 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698296 | GGGCCCCATGAGGGC[C/T]GGTCGGGGAGACCCT | 54442 |
rs377758823 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2683379 | AGATGCGTCCGTAGT[A/G]TATAGTATGATTTTT | 54442 |
rs386787838 | multinucleotide-polymorphism | ATCA/GACG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2686964 | TTAGTGGGTGTCTGC[ATCA/GACG]CTGATGGACTTTGTT | 54442 |
rs397831541 | in-del | -/AG | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700641 | CCTCCCTGTCCTGAG[-/AG]TTTCCTCTGTCACTT | 54442 |
rs397855171 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700813 | TGGAGCCCCCCCCCC[-/C]CTTAAAATGTCACTA | 54442 |
rs397855247 | in-del | -/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700814 | TGGAGCCCCCCCCCC[-/C]TTAAAATGTCACTAA | 54442 |
rs527239838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706970 | GGGACTGGACTGCTG[A/G]GGGACCCGCGGGCCG | 54442 |
rs527327129 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | KCTD5 | GRCh38.p7 | 16:2707324 | ACGAGGCTCAAGGAT[A/G]TGAGGGACACAGTAT | 54442 |
rs527328247 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702537 | GAAGGCTCTTGCCCT[C/T]TCAGACCTTCCTCCT | 54442 |
rs527418399 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700513 | GCTTGTCATCGGGGA[C/T]CTCAGGACACGTGAG | 54442 |
rs527448118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698728 | CGCTCCTAGCCTGGC[C/T]GCTCAGGGCCGCTGG | 54442 |
rs527558907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702971 | GGGCCTCATCTTTGT[C/T]GAGAGGAGGGTGTCC | 54442 |
rs527782031 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698132 | AGACCCTTGTCCTCT[C/G]TCACTGCCCCAGTGC | 54442 |
rs527783356 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693228 | GCCATGCTGAGGGCA[C/G]TGGGCTATGGTGTGG | 54442 |
rs527894515 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687330 | TTCGGGGCACCTGAC[A/G]TGGGCCCGCGGTCTT | 54442 |
rs527970888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691591 | GAGGTCGTGGGGCTC[A/C]GAGAATTGAACCACG | 54442 |
rs528057156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700001 | TCAGTGCTCCTGGAA[A/G]TGCAGACTTTGCTGC | 54442 |
rs528078904 | snp | C/T | 0.197531 | 0.244432 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2695958 | AGGCGCCTATTTAAT[C/T]GACAGAGACCCCACC | 54442 |
rs528223646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693845 | CCCCCACCTTTTGCT[C/T]GTAAAGAAACTGAGG | 54442 |
rs528230374 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682350 | CCATCAGCGTTAGTG[C/T]CCAGATCACCCCGTG | 54442 |
rs528366871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690029 | ACCTGTCCCTGAGAG[G/T]CTGGGGAACCCCCAC | 54442 |
rs528409385 | snp | C/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708233 | ACGGTGAAAATTCGG[C/G]ATGTTTACAGAGCAT | 54442 |
rs528415291 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690273 | TGTGCCCTGGCTCGG[C/T]GCTGTCTGCCATGTG | 54442 |
rs528512886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682932 | TCGAGCCCCGCGCTC[C/T]CTTGTCGCCAGCTCC | 54442 |
rs528590069 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687845 | CCTTGTAGCAAAGGT[A/G]CCAGCAAGCCATCTC | 54442 |
rs528625757 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688346 | ACCTCTGCCTCCTGG[A/G]TTCAAGCATTTCTCC | 54442 |
rs528651581 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708289 | TCTCATTTTCTTTGT[A/G]TAACTATGCAGCCTT | 54442 |
rs528779822 | snp | A/C | 0.00080032 | 0.019988 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707896 | CATTCCGAGGCCGGG[A/C]CTTCTTCTGACACGG | 54442 |
rs528876295 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680504 | GCTCACTGCTGAGAC[G/T]TCAGAGATCGCAGCT | 54442 |
rs528940698 | snp | A/C/T | 0.00438571 | 0.0466605 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691283 | GCGGATGTCCCTGAC[A/C/T]TTCCGCTCTGCCCAG | 54442 |
rs528953410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685278 | TAAAAATACAAAAAA[A/C]TTAGCTGGGCATGGT | 54442 |
rs528994002 | snp | A/G | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707771 | CGACCACCAGGCCCT[A/G]GTCTCGGTCAGGGAG | 54442 |
rs529059597 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706305 | TGCCCTCTCTCCGGT[C/G]AGTGCGGCATGGCAG | 54442 |
rs529061920 | snp | G/T | 0.00349761 | 0.0416722 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698040 | TTGTATGGCTGGTGT[G/T]AAGGAAGGGCTCCCC | 54442 |
rs529157518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705926 | GGGCTCCCGGATGCT[C/G]AGATGCCACACTGCT | 54442 |
rs529158621 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681069 | TAGAGCTGCTGTAGC[C/T]GTTCCTTCACAACAT | 54442 |
rs529223890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705049 | TGGAAGGTCACCGGG[C/T]GTGGGGGTTTGGGCC | 54442 |
rs529260044 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705336 | TAGCACTGTCTTGGT[C/G]GTGGGGCTGTTGCTG | 54442 |
rs529261385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700577 | ACCTGGCTGCCACTG[A/T]TCCTGGTGCTAGACA | 54442 |
rs529512863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697369 | AAGAGCTGGAAGTGA[C/T]CCTCTCAGCCAGCCA | 54442 |
rs529541192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701058 | GCCGTGTCAGCAGCT[C/T]GGGGTCCGCGAACAG | 54442 |
rs529612980 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703055 | CCTGGCAGCACCGGC[A/G]CAGACTCTGCGGGGG | 54442 |
rs529627975 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707716 | CTGGCAGGAAGCGGC[C/T]GCAGCCGCGTCAGTG | 54442 |
rs529922450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688366 | AGCATTTCTCCTGCC[C/T]CACCCTCCCAAGTAG | 54442 |
rs530082601 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706301 | CCACTGCCCTCTCTC[C/T]GGTCAGTGCGGCATG | 54442 |
rs530126328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692246 | GAAACGTCTCTGGCC[A/G]GCAGCACCTTTGTCC | 54442 |
rs530212544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697828 | CAGGGGCAGGGGCAA[A/G]GGCAGGGGTGGGTGT | 54442 |
rs530214986 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682379 | TGCTCCGCTCCCGCC[A/G]GAAGCGGGCCCAGCC | 54442 |
rs530216796 | snp | A/G | 9.99534e-05 | 0.00706871 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702451 | CACCCCGTACGGTAC[A/G]GCCAGCGAGCCCAGC | 54442 |
rs530249992 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698288 | GGGAAGGAGGGCCCC[A/C]TGAGGGCCGGTCGGG | 54442 |
rs530370955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687754 | CAGCCCCCCTCCACG[C/G]CCCAGGTAAGCAGTC | 54442 |
rs530448457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690340 | GGCAACTGTCCTGCC[C/T]GGCCTACGTCCTGTG | 54442 |
rs530616459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700450 | TCTTCAGCAGCTTCC[A/G]CGGAAGCCACCTGAG | 54442 |
rs530620529 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696212 | TGAGGCCACGGGCAG[C/T]GGCGCAGCTGCCGGA | 54442 |
rs530659959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696719 | TGGGCAGCGTCTGAC[C/T]CCGTTTCTGTTCTGG | 54442 |
rs530868071 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688717 | CCAGTCCCCCTGCTG[C/T]CACCCAGAGCTCTGG | 54442 |
rs530979297 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708402 | TTAGAAACCGCTGCC[C/T]GCATGCTTTGAAAAC | 54442 |
rs530984033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704592 | AGAGAGAGACAGGCT[C/T]AGATCAGCAAGGGCG | 54442 |
rs530985218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682971 | TTGCCCCGATCCCCT[A/G]CCCTGGGAGGGGAGG | 54442 |
rs531073247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683326 | GCGCTCCATCCTTTC[C/T]ATCCACAGCACGCAG | 54442 |
rs531219435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704124 | TTTGTGGTTGAGAAT[A/G]TGGCCCTATTTCATT | 54442 |
rs531248911 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706321 | AGTGCGGCATGGCAG[C/T]GACCTCTGGGAGGCT | 54442 |
rs531409819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702833 | GACTTGGGATGCTGA[A/G]GCCTGGCTGTCATAG | 54442 |
rs531485159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702204 | TCGTGCAGGTGTTCC[A/G]GGGATTTGTTTTCCA | 54442 |
rs531537876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698301 | CCATGAGGGCCGGTC[A/G]GGGAGACCCTGAGGT | 54442 |
rs531579373 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701109 | TGTGCTCTTCTGCCA[C/G]CGTCTTGTGACTTCT | 54442 |
rs531606234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697133 | TGTGTCTCTGAGGCC[C/G]TCGTCTCCTTGTCTC | 54442 |
rs531739584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701668 | CAAAGTGTGAGCCTC[A/G]TCCAGCTGCTTTTTG | 54442 |
rs531754708 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699414 | GCCTTTTTCTGGTAG[C/T]TGGGAGCGAGCTTCG | 54442 |
rs531809956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691564 | AGCCTGGGTAGGTCC[C/T]GCATGGGCCCAGAGG | 54442 |
rs531834993 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691500 | CTGCAGTGTCACTCC[A/G]GGAGAGGGCTGTGGG | 54442 |
rs531836026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686582 | CCACTCAGATGGAGG[A/G]GAATTTGGGGAGGCT | 54442 |
rs531916324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691333 | GAAACCCACCAGTTA[C/G]AAGGAACCCATGGGA | 54442 |
rs531978220 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703946 | CCTCTTGGAGCAATC[A/G]TAGGGCTCTTTTCTA | 54442 |
rs532016374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699651 | AAAACAGCAGCTGTT[C/T]GGGCCGCGTGTTTTG | 54442 |
rs532096085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699161 | TTTCCGTCCAGCCCC[A/G]TCTGCAGCCTGAGTC | 54442 |
rs532190931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689956 | GCTGGGATCACAGGC[A/G]TAAGCCACTGTGCCC | 54442 |
rs532213344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703546 | GGCCACCAGCAGCCC[A/G]GGACTGTCCCCGTGA | 54442 |
rs532263752 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693811 | ACTCATGGCGGCCCC[A/G]AGCTACACGAGCTGG | 54442 |
rs532298126 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689518 | TCCCCTCTGGTGGCA[C/T]GTGTCTCCGAGCACC | 54442 |
rs532299993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695521 | GGAGCGCAGGCCCAG[C/G]CTGGTGGCCATCAGA | 54442 |
rs532435091 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691280 | GGTGCGGATGTCCCT[A/G]ACCTTCCGCTCTGCC | 54442 |
rs532435671 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692781 | CATGGCGCCTGGGCT[C/T]GGCCCCAACTTTGCT | 54442 |
rs532642774 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698650 | AGTGGGGTGTGTGCC[A/G]CACTGTGGCCGCGGC | 54442 |
rs532688840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692849 | AGGCAGTGAGAGCAG[A/G]CACTTCTGAGCCTGC | 54442 |
rs532743814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682898 | GACTTCAGCGGGAGC[A/G]GGCGACTCTCCTCGG | 54442 |
rs532803117 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682470 | AGGGCGGACCTGTGG[A/G]CGGGACAGAACTCAG | 54442 |
rs532816886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688279 | TATTTGAGACGGAGT[C/T]TTGCTCTGTCCCCCA | 54442 |
rs532972602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685191 | AGCACTTTGGGAGGC[C/T]GAGGCGCGTGAATCA | 54442 |
rs533061074 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705004 | GGCAGAGCCCCTGAG[C/T]CTGTGTGTCCCCTCG | 54442 |
rs533085846 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690730 | TCCTCGTGTCATGGG[C/G]GCTTGGGCAGGCGCC | 54442 |
rs533109229 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709089 | CACCCCGGGTCGCTC[A/G]GACCAAGGTGCTGCC | 54442 |
rs533193109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704656 | CTGGGCGGCTGAGGA[A/G]GGGGTTCCTTGGTGG | 54442 |
rs533212683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685887 | ACCTGGGCTTGCAGA[A/G]TGTGGGGGTCTGGAG | 54442 |
rs533332828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700536 | CACGTGAGGCATGGC[C/T]TCTGACCGGGGGGCC | 54442 |
rs533426680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705008 | GAGCCCCTGAGCCTG[C/T]GTGTCCCCTCGTGGC | 54442 |
rs533516876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702273 | TCGCGGTGGCAGGCG[C/T]GTCCTGAGGCTGGTC | 54442 |
rs533578280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700987 | GAACAGAAATCTTTG[A/C]TGCTGGGCGAGCCCC | 54442 |
rs533635402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702010 | TTTCAGAGCCGCCCT[C/T]CACTCTCCTCCCGCT | 54442 |
rs533715008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692487 | CAGCAGAGAGGGTAG[C/T]TTCCCTCTGCAGCTG | 54442 |
rs533823105 | snp | A/G | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681765 | TTTTTTTTTTGAGAC[A/G]GACTCTCGCCCTATC | 54442 |
rs533913587 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703674 | CTTTCCACCTCAGGC[A/G]ACTGTCCTGGCCCAG | 54442 |
rs533937717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691359 | TGGGAAGAAACGGCC[A/G]GAGAGCTGTGAGGCC | 54442 |
rs533937748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685407 | ACTCCAGCATGGGCG[A/G]CAGATCGAGACTCTG | 54442 |
rs534073183 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691866 | CCTCAGCCTCCCCTG[A/C]CTTTGATGGCTGGGT | 54442 |
rs534212592 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686737 | GGGCAGTCAGGGTGC[C/G]TCTAACAGTGTACTG | 54442 |
rs534279174 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697144 | GGCCCTCGTCTCCTT[A/G]TCTCTATCCTGCGTG | 54442 |
rs534336943 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689584 | GCAGAGCTCTGGGAG[C/G]TGCGGGAGGGTTGGG | 54442 |
rs534443284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688431 | GATTTTTGTATAGTC[A/T]GTAGAGAAGGGGTTT | 54442 |
rs534457673 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688481 | GTCTCGAACTCCTGA[C/T]CTCAGGTCATCCGCC | 54442 |
rs534479364 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708540 | GTGCAGACTGACCAC[C/T]GGCCTCCCGCCTGCA | 54442 |
rs534522178 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691753 | AGCCTTGGCTCCCAG[C/T]GAGGTTGGCAACAAG | 54442 |
rs534538060 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680655 | AGCACACGTGGCAAG[C/T]GCCTGAATCGGGGCT | 54442 |
rs535029111 | in-del | -/CTTTTT | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681746 | TATTACAAAAACTTT[-/CTTTTT]TTTTTTTTGAGACAG | 54442 |
rs535045552 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703774 | CTCGAGGCCGAGGCA[A/G]TGTAGGCTGGGGCAG | 54442 |
rs535301649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691044 | CCCGCACACATTAGG[C/T]CGATCTGGAACATGT | 54442 |
rs535397997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705140 | ACGCCGCCAGAGTGA[C/T]GACGAGGACCAGGGG | 54442 |
rs535489529 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696552 | GGACGGCGCCCACAC[A/G]CGTTGGGCCCAGGCT | 54442 |
rs535541380 | snp | A/C | 0.000232169 | 0.0107717 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699808 | CCCTTACCTGTGCCC[A/C]TTGTCCTTGCAGGTG | 54442 |
rs535705605 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2701111 | TGCTCTTCTGCCACC[A/G]TCTTGTGACTTCTGG | 54442 |
rs535768185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690141 | AGTCTTGTTACCACA[C/T]TTCTCTGAGTGTTGC | 54442 |
rs535769489 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2703187 | GACCCATTCTGGTGG[C/T]ATTTCCTCTAAGCAC | 54442 |
rs535924697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702585 | AAGCTCCCGGTGTCC[A/G]CCCCTGGTGGCCTTG | 54442 |
rs535928468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698128 | CCTGAGACCCTTGTC[C/G]TCTGTCACTGCCCCA | 54442 |
rs536076062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684806 | AGCCAGGTGTGGTGG[C/T]GCGTGCCTGTAGTCC | 54442 |
rs536140820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696863 | TCCTGTCTCTTTGGC[A/C]GGGAATGTCTTTCAC | 54442 |
rs536181322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690447 | GCCCGGCCACAAGTA[C/G]GTCAGATGCCAATTC | 54442 |
rs536188691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687891 | TTGTTCTCCCTGGGC[A/G]TCAACTCGGCAGTTC | 54442 |
rs536256949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692588 | TGGACCCAGAGGGAA[A/G]GAAGTGCATACTAAT | 54442 |
rs536303649 | snp | A/G | | | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709464 | CGTGAGCCATTGCGC[A/G]CGGCTCAAGTGATGT | 54442 |
rs536314439 | in-del | -/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681747 | ATTACAAAAACTTTC[-/T]TTTTTTTTTTTTGAG | 54442 |
rs536367090 | snp | A/C | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681741 | GGCTTTATTACAAAA[A/C]CTTTCTTTTTTTTTT | 54442 |
rs536489328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706980 | TGCTGAGGGACCCGC[A/G]GGCCGAGTTGCGCTT | 54442 |
rs536494152 | snp | C/T | 1.66396e-05 | 0.00288436 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702328 | GGCTTCACTGGGCTG[C/T]GTCTCAGGCTATGTC | 54442 |
rs536498245 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706362 | AGGGCGTGGGCGTTG[C/T]TGCCCTACCTGGTGT | 54442 |
rs536506473 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681320 | TGTTATTTAAATTCT[C/T]TTTTTTTCTTGAGAC | 54442 |
rs536744293 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689671 | CCTCATTCCTCACTG[C/T]CGTTTTCTTTTCTTT | 54442 |
rs536783816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683987 | CCTCCCCACAACTTC[C/T]AACTGTTTCCATTGC | 54442 |
rs536800121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704771 | CCACCCTCCCTCCTG[A/C]AGCAGTGGGGCCAAT | 54442 |
rs536813157 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706445 | GAGGCTGGCTGGCTC[C/T]GAAGCTCTCTGCTCG | 54442 |
rs536887303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700261 | CCACTATCCAGCGCA[A/G]TCCCCGTCCCCCACA | 54442 |
rs536939320 | snp | C/T | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681354 | GTCTCACTCTGTCGC[C/T]CAGGCTAGAGTGCAG | 54442 |
rs537072345 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684389 | GGTGGCTCATGCCTG[C/T]AATCCCAACACTTTG | 54442 |
rs537078340 | snp | C/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708608 | CTGGAGACTTCCTGC[C/G]TAGGCCTCATCCTCC | 54442 |
rs537165703 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2706254 | GCCTCCAGGAGCCTT[C/T]GGAACAAGCCTGGGG | 54442 |
rs537405540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703255 | CCATCCAAGCAGAAT[A/C]TGACCTTGGCCTGGG | 54442 |
rs537561312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705622 | TCCCTGATGCGCTTA[A/T]GCCTCCCAGGCCAGC | 54442 |
rs537569717 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707543 | GGGAGCACGGCGGCC[A/G]GGTGGGCGCTGCCTC | 54442 |
rs537614843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693596 | GTTTCCGCCGATGGC[C/T]GTCCCCACCCTGCCC | 54442 |
rs537646712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686892 | TAGTGGAGATGGCAG[A/G]TGATGTTCTGTGTAG | 54442 |
rs537651912 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694013 | CTGCCAGCGGTCTGT[C/G]GAGGTAGCAGTGAGC | 54442 |
rs537663339 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688489 | CTCCTGACCTCAGGT[C/G]ATCCGCCCTCCTTGG | 54442 |
rs537803174 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705989 | ACAGGGCTGGTGGGG[A/G]CTTGGGGGCTGCACT | 54442 |
rs537814444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696928 | TGTTGTCGTGGAGCC[A/G]CTCGAGTCGAGGCTT | 54442 |
rs537853094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690485 | CGCGGGGAAGATGAG[A/G]GAAATGACTTGTCAA | 54442 |
rs537890567 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701836 | CCTGGACCTGCATTG[G/T]CCTGGCCTGCCTGGT | 54442 |
rs537925986 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696612 | GGCTCAGAACAGCTC[A/G]AGGCCTCGCCGTGAA | 54442 |
rs537928022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700637 | CCAGCCCTCCCTGTC[C/T]TGAGTTTCCTCTGTC | 54442 |
rs538002395 | snp | A/G | 0.000100413 | 0.00708496 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697885 | GGTCTGGTAAAGACA[A/G]TTTATTTTTCCTTAT | 54442 |
rs538041050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691706 | CAGGTTCTTGGTAGA[C/T]GCAGCTGGGGTTCTC | 54442 |
rs538145791 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684809 | CAGGTGTGGTGGCGC[A/G]TGCCTGTAGTCCCAG | 54442 |
rs538210416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693119 | TGGCTGGGTCCTCAC[C/T]GCTGGTGCCACTCTC | 54442 |
rs538249220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687973 | GAGCATCTTCCTTGG[A/T]GTTGGGGAGCCTGGG | 54442 |
rs538282177 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2691992 | TTCCCACACAGGTGC[G/T]TCCGGGGGCTTCCTG | 54442 |
rs538331235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698924 | TCCCTGCCTCAGTCT[A/G]CCTACCTGTATGACG | 54442 |
rs538421026 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2705292 | TTGACGAGAGCCGTC[C/T]GCACTCCATGCCAGC | 54442 |
rs538469297 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688138 | CGCCCCGTACCTGGT[A/G]CCAGGTCAGTGCAGT | 54442 |
rs538536558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688398 | TGGGATTACAGGCAC[A/G]AGCCACCATGTCTGG | 54442 |
rs538905306 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703128 | AATGCAGGGACCCCT[G/T]CCTCGTTTGCTTTCA | 54442 |
rs538915638 | snp | A/C/G | 0.000118254 | 0.00768851 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2682752 | CCGGGACCCGAAATC[A/C/G]TTCCTGTACCGCTTA | 54442 |
rs539060155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706568 | CCTGTCCTCAGGGGA[G/T]CCCAGGCCGACTTGG | 54442 |
rs539149499 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681351 | GGAGTCTCACTCTGT[C/T]GCCCAGGCTAGAGTG | 54442 |
rs539151084 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684491 | ATACAAAAAGGTGGG[C/T]GCGGTGGCTCACGTC | 54442 |
rs539173875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702626 | GGACACACGGTCTCC[C/T]GTGGGACAGGTTCTC | 54442 |
rs539211535 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700737 | TCAGCCAGTGTCCCT[C/T]TGAATGAAAGCTACC | 54442 |
rs539264326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698498 | CCTTCTGCAGCCAGG[A/G]GAGCCCAGGTTGTTG | 54442 |
rs539354734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707043 | AGGCCCAAGAGTCAG[C/T]GCCTTTGGGTGGGTC | 54442 |
rs539370256 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2699302 | GAGGGGCACAGCAAG[C/T]GTGCCAGGCAGGTGG | 54442 |
rs539486923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699735 | TGCAGAGTGGACCTC[A/G]GCCTCCCTGGGTCAC | 54442 |
rs539644708 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700858 | CCACCGTCCACCCTG[A/G]ACCCCTAGGCCGGGG | 54442 |
rs539715727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701314 | CTCCCAGTTCATGTA[A/G]GGAAGCCGCTGGGCT | 54442 |
rs539758186 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705120 | TCTCCCCCACTGCGC[G/T]CTGCACGCCGCCAGA | 54442 |
rs539775370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699396 | TGCCGCGCAAGTTCA[A/G]GAGCCTTTTTCTGGT | 54442 |
rs540007711 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696540 | ATCGTGGTGCAGGGA[C/T]GGCGCCCACACGCGT | 54442 |
rs540042830 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690122 | TGAGATGAGCAGAGC[C/G]GCCAGTCTTGTTACC | 54442 |
rs540060318 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681382 | CAGTGGCCTGATCTC[A/G]GCTAACTGCAACCTC | 54442 |
rs540101010 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700176 | TCTTCCCAGCGCTGC[A/G]CTTTCTTCGCATCAT | 54442 |
rs540118134 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | KCTD5 | GRCh38.p7 | 16:2694125 | CCCTGGACTCGGGTG[A/G]CAGCACTGGCCGCCT | 54442 |
rs540203953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684877 | TGGGAGGTGGAGCTT[A/G]CAGTGAGTCAAGATC | 54442 |
rs540205994 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691242 | GAGAGCAGCACCTCC[A/C]CACGCCACTGCCTCC | 54442 |
rs540239799 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685958 | GAAACCACAGAAGCT[G/T]TGGGTGCCTGAGAGG | 54442 |
rs540241763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691536 | CTGCAGGCCCGGCGC[A/G]CCGAGTCCACGCAGC | 54442 |
rs540433102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701008 | GGCGAGCCCCACCTC[C/T]CAGTTGTCCCTTGGT | 54442 |
rs540466129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706272 | AACAAGCCTGGGGTG[G/T]CATGCACCTCTCACC | 54442 |
rs540550339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705307 | CGCACTCCATGCCAG[C/T]TGTAGATCCTCAGTA | 54442 |
rs540553082 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681003 | TGCTGGTAAAAGCCT[A/C]TATTACGACTGTTAA | 54442 |
rs540701877 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707700 | AGCAGCCTGGGCTTC[A/G]CTGGCAGGAAGCGGC | 54442 |
rs540721782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688090 | TTACTTTACTGTGAC[A/G]TCCTCTCCTGAAGAT | 54442 |
rs540723793 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682362 | GTGCCCAGATCACCC[C/T]GTGCTCCGCTCCCGC | 54442 |
rs540758753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682825 | TCACGGGCCAGCCCG[G/T]AGGGTCCTGGCCTTC | 54442 |
rs540785067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703831 | AAGCTGGGGTTCCAC[C/T]GCCAGGCTCGGAGAT | 54442 |
rs540946796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703441 | GTTGAGTGGGTGCCA[G/T]GAGAGGCCAGAACCG | 54442 |
rs541059907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704717 | ATGGGTGCATCCACC[A/G]CCTGCCCCCGTGGCT | 54442 |
rs541182528 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699095 | CCCTGGCATGAGTCA[A/C]CACCTTAAGGTCAGG | 54442 |
rs541399652 | snp | C/G | 3.32602e-05 | 0.00407786 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2702439 | GGAGCTGCACAACAC[C/G]CCGTACGGTACGGCC | 54442 |
rs541468143 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2700104 | GAGTTCGGGTGGGGT[A/G]GGCAGAGGTGTCTCA | 54442 |
rs541485896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702682 | TGCGGCCTCCCAGCC[G/T]GCATGCAGAGCTGCT | 54442 |
rs541561431 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706691 | AGGGGGCCGAGGGGC[C/T]GTGGGCTCTGCAGGG | 54442 |
rs541694166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692078 | GCCACTGTGGCCAGA[A/G]CTCTCACTGCCAGCA | 54442 |
rs541805016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700310 | TATGGAGGCCCTGAC[A/G]CCTTTCCCAGGCTGC | 54442 |
rs541831961 | snp | A/G | 0.188316 | 0.242271 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688696 | GGCCAGGAGTGGCTC[A/G]CCCTGCCAGTCCCCC | 54442 |
rs541944623 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693716 | CACCGGCCCAGGGCC[C/T]GAGAAGCACATGGTG | 54442 |
rs541968409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704894 | CCAGGCGCCTCTGGA[C/T]AGGGTTCAGCCCCTC | 54442 |
rs541982366 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690682 | CTCCTCATCCCAGTC[G/T]TAGAGGCGTGAGCGG | 54442 |
rs542025786 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690462 | GGTCAGATGCCAATT[C/T]AGTGAGACGCGGGGA | 54442 |
rs542092954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697037 | CTCACCGGTCTGCCT[C/T]TATCCCGCCCCGATG | 54442 |
rs542176486 | snp | G/T | 0.146608 | 0.227618 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695219 | CAGTGCCTCTCAGGG[G/T]TCCCTCCACCCAGGT | 54442 |
rs542215206 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689871 | AGTAGAGACAGGGTT[C/T]CACCATGTTGGTCAG | 54442 |
rs542270170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687237 | CTCTGGTGATGAAAT[G/T]GAACGTTTCTGATGG | 54442 |
rs542441190 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709317 | CCCATCCCGGGAGAC[C/T]GGAGACCATGTACAA | 54442 |
rs542484914 | snp | C/T | 0 | 0 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707237 | GTTTTCTGGAGCAGG[C/T]GCCTGGTCAGGGACA | 54442 |
rs542655535 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681077 | CTGTAGCTGTTCCTT[C/G]ACAACATGAAATAGG | 54442 |
rs542694182 | snp | C/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687010 | TGAGGATGTGGCTCT[C/G]AGCACGATCTTCGCT | 54442 |
rs542710881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685515 | GCCAAAAGTGTAGTG[A/C]TAATTCATATTAGTC | 54442 |
rs542766121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697473 | CCCCACACAGCACCC[C/T]ACCCAGTGGCGTGGC | 54442 |
rs542772349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702064 | CAGGGACCCGTCTGT[G/T]CTCCGTCCCCCTGGG | 54442 |
rs542801365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706717 | CAGGGCTGACGTGGT[A/G]CAGATGAGGAGGGGA | 54442 |
rs542860489 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697757 | CACGTCTGCAGGAAG[A/C]CTGTTAGGTCGGGGC | 54442 |
rs542929803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701636 | CGTTGGTCCAACTGC[A/G]CAGGTCTTAGAGAGG | 54442 |
rs542941750 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681545 | TTGAACTCCTGACCT[C/T]GTGATCCACCCACCT | 54442 |
rs542971908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706131 | GTGAGTGGGAGCCTC[A/G]AGCTAGAAGTGGTCC | 54442 |
rs543036752 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705761 | CTGTGGAAGATGGCC[G/T]AGGGAGACAGTGTGT | 54442 |
rs543080180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703943 | CTTCCTCTTGGAGCA[A/G]TCGTAGGGCTCTTTT | 54442 |
rs543164096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693743 | GGTGGGTTGTCTTGG[C/T]CTAGAGGTCACGGCT | 54442 |
rs543168358 | snp | C/T | 4.9836e-05 | 0.00499154 | synonymous-codon | KCTD5 | GRCh38.p7 | 16:2699910 | CGACGGCTGGAAGTT[C/T]GAGCAGGTGAGGGGC | 54442 |
rs543250902 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695387 | CCTCCCTCGCTGCTG[G/T]CTCCCGGCCTGTTGG | 54442 |
rs543330099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699543 | TCGTGTCGTCATGTC[A/G]AGCCACAGGTGCTCT | 54442 |
rs543426311 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707631 | CCAGTCAGCCCGCTC[A/G]ATCCTGAAGATCGTG | 54442 |
rs543504132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683092 | GTGGAGGAGGCTTCC[G/T]AGACCCCGGACTTTG | 54442 |
rs543569944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702773 | GTGTCTCAGGGGACC[C/T]AGGGTCCTCTGTTCC | 54442 |
rs543650163 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2702068 | GACCCGTCTGTGCTC[C/T]GTCCCCCTGGGGCAG | 54442 |
rs543655480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2682868 | TCCTGCACACGCCCT[A/G]CTTCGTGCGGAGGAG | 54442 |
rs543718003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704366 | CAGCATGTGTGGCCT[G/T]GCCCTGCTGGGCAGC | 54442 |
rs543833563 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697421 | TCAACTGAGGTGCCA[-/G]GTGACTGAGACATAT | 54442 |
rs543839011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692802 | CAACTTTGCTCCAAG[A/G]TCGGAGCAGGCACCA | 54442 |
rs543862338 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692133 | AAGGTGCCATGGCTC[C/T]GGCTGGTAAACTTGG | 54442 |
rs543877717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698977 | GGTGGGAGAGTCTGC[G/T]GTCCAGCCTTGCTGT | 54442 |
rs544070266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687756 | GCCCCCCTCCACGCC[C/G]CAGGTAAGCAGTCCC | 54442 |
rs544106881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693343 | GCTGCTGGCATCACC[A/G]CACTGGGCCAGCTGT | 54442 |
rs544155422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685098 | AGAACATGAAGGTAA[A/C]GTAGCAGATACAGTC | 54442 |
rs544244411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684194 | TACTCAAGCATTCCT[A/G]TTTTGTATATGAAAT | 54442 |
rs544262146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697240 | GGGGTCCTGGAGGAA[G/T]GAAGACCACCCATGA | 54442 |
rs544263892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690703 | GCGTGAGCGGGCCGG[C/G]GCATCTTTCCTTCCT | 54442 |
rs544272228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690928 | TTGTTTCTGCATCAG[G/T]GTGGAGGCTGATCCA | 54442 |
rs544360175 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685593 | GTAAAATGCTTCATC[G/T]TAGTTTTGTCTCCAG | 54442 |
rs544467969 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704963 | TGCAGCCGCCTCACA[C/T]GTGGAGGTTTCCACC | 54442 |
rs544495254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691152 | CTGGTGGGATTTGGG[A/G]GTCCTGGTTTAAGAC | 54442 |
rs544506112 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709463 | GCGTGAGCCATTGCG[C/T]GCGGCTCAAGTGATG | 54442 |
rs544560276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690224 | GAGCAGTCAGCTCTG[C/T]CTGCGGAGTCTTCCT | 54442 |
rs544594973 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684581 | CCATCCTGGCTAACA[C/T]GATGAAACTCTGTCT | 54442 |
rs544627439 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2688532 | CTGGGATTACAGGTG[A/T]GAGTGTACTTTACTT | 54442 |
rs544638038 | in-del | -/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682233 | TCTTCCTTTGACCAG[-/T]TCATGAACTGGAGTC | 54442 |
rs544733554 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687098 | GCTCCCCGCTCCTTC[C/T]CCACTGCAGCAGGTG | 54442 |
rs544901384 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703374 | CTGGGTGGTGGGGCG[G/T]GCTCTGTGGGGAGCC | 54442 |
rs544904362 | snp | C/T | 1.65597e-05 | 0.00287743 | intron-variant | KCTD5 | GRCh38.p7 | 16:2707277 | CCCAAGTCCTCATTT[C/T]ATGCATTTGGTGTTT | 54442 |
rs544954992 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681650 | TATTGAATTCATGTT[C/T]GGGGCCACGTTGTTA | 54442 |
rs545018955 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691535 | GCTGCAGGCCCGGCG[C/T]GCCGAGTCCACGCAG | 54442 |
rs545067031 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687260 | TCTGATGGGTTCAGT[C/G]CTACCTAGGAAGAAT | 54442 |
rs545152849 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2691581 | CATGGGCCCAGAGGT[C/T]GTGGGGCTCAGAGAA | 54442 |
rs545178658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702948 | GTACCCTGGCTCAGC[C/T]ACTACGTGGGCCTCA | 54442 |
rs545217292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698662 | GCCGCACTGTGGCCG[C/T]GGCTGCCATCAGAAG | 54442 |
rs545238713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692035 | GGAGCCTGAGCTCCA[A/G]GGACTGAGACGAGCT | 54442 |
rs545250672 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709052 | TAGTAGCTGTTTATG[A/G]TCTTAAGATGCAGGG | 54442 |
rs545312850 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697773 | CTGTTAGGTCGGGGC[C/G]TGAGCAGCTCCCGCT | 54442 |
rs545373086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706181 | GCACCCGCCTGGGAA[C/T]GGCAGAGCTGTTGGG | 54442 |
rs545528605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699974 | GAACTTGTGCTCACA[A/C]TGGCTCAGGGCTCAG | 54442 |
rs545763719 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | KCTD5 | GRCh38.p7 | 16:2695719 | GAGACTTAAACTCAC[G/T]TAGACCTGGGGTGGT | 54442 |
rs545776993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704408 | TCAGTCAGCGGCGGC[G/T]GGAGAGCCTGGGTGG | 54442 |
rs545841908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704854 | TCTGTGGGCTAGCGC[C/T]GCCTGCCAGGAGTGG | 54442 |
rs545919081 | snp | A/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692791 | GGGCTCGGCCCCAAC[A/T]TTGCTCCAAGATCGG | 54442 |
rs546047777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683260 | AACGCTGACGTGGGG[A/G]TTGATATGGGCGGCC | 54442 |
rs546383188 | in-del | -/CT | 0.0138799 | 0.0821421 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684589 | GCTAACATGATGAAA[-/CT]CTGTCTCTACTAAAA | 54442 |
rs546383484 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684096 | GTTAGCTGTGATTTT[C/T]CTTTTATAAGTGTGG | 54442 |
rs546418270 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696591 | GTGTGCTGCGGTGCT[-/G]GGCTTGGCTCAGAAC | 54442 |
rs546456358 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708267 | AAATGCCTCTCTCTC[A/G]CCGCTCTCTCATTTT | 54442 |
rs546497297 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688502 | GTCATCCGCCCTCCT[C/T]GGCCTCCCAAAGTGC | 54442 |
rs546584396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704658 | GGGCGGCTGAGGAGG[A/G]GGTTCCTTGGTGGTG | 54442 |
rs546591052 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685197 | TTGGGAGGCCGAGGC[A/G]CGTGAATCACCTGAG | 54442 |
rs546625335 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705018 | GCCTGTGTGTCCCCT[C/T]GTGGCGTGGCCTCAC | 54442 |
rs546629535 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687577 | CGGATTGTGTGTGGC[C/T]GTTTTTGCTCTGAAA | 54442 |
rs546660122 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708499 | AAGCGCTTTGCTTCC[A/G]GAACTCCGGCTTCCC | 54442 |
rs546699505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690796 | TAGGTTGGCCCAGAC[A/G]CTGTTCTAAACCTCC | 54442 |
rs546716061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700177 | CTTCCCAGCGCTGCG[C/G]TTTCTTCGCATCATC | 54442 |
rs546848392 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701723 | CTTATTGTGATTTGC[A/C/G]TATTGCCTTTTAATT | 54442 |
rs546923590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705492 | AGTGCCACTCGTGCC[A/G]CCAGCCCTAGTGGGT | 54442 |
rs546984670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702577 | TTCTCATCAAGCTCC[C/T]GGTGTCCGCCCCTGG | 54442 |
rs547237841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693001 | CCATAGTTTGGGTGG[C/G]GCGAACCCCAGGGCT | 54442 |
rs547260786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690420 | TGCTGGGCCCACTCA[A/G]TGCCAGCTTGGGCCC | 54442 |
rs547296374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700543 | GGCATGGCCTCTGAC[C/T]GGGGGGCCCTTGCCC | 54442 |
rs547404303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698403 | GGGTCGTGTGGGTCT[C/G]CGCAGGCGCCAGAAG | 54442 |
rs547436040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697814 | ATGGGCCCTCATTGC[A/G]GGGGCAGGGGCAAGG | 54442 |
rs547594223 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681745 | TTATTACAAAAACTT[G/T]CTTTTTTTTTTTTTG | 54442 |
rs547619798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693470 | AGGAGTGGCCAAGAC[A/G]CGGCAGCGGCCTACC | 54442 |
rs547792615 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700276 | ATCCCCGTCCCCCAC[A/G]GCTCACTCCATCGGA | 54442 |
rs547837115 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2689587 | GAGCTCTGGGAGCTG[C/T]GGGAGGGTTGGGCAG | 54442 |
rs547894663 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697576 | TACCATGGCCTCGGC[A/G]TAGACATACGCTGAG | 54442 |
rs548068319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684362 | CTTTGTTAAAAATTA[C/T]GGGCCAGGCGCGGTG | 54442 |
rs548083036 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698894 | CCCTGTTGTGTGACC[-/G]GGCTGTGTGGGCACT | 54442 |
rs548129677 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696097 | GGCAAGGGCCCGACA[A/G]AGGTGCCAAGGGCTC | 54442 |
rs548216460 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690044 | GCTGGGGAACCCCCA[A/C]GTTGCCCCCGGTGCT | 54442 |
rs548326051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700048 | TTCTGGGGGTGCTCA[C/T]GGCAGCGACCTGTGC | 54442 |
rs548796965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704066 | GCTGCAGAAAGGACA[C/T]GCTCTGTACTGTGAG | 54442 |
rs548834042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699659 | AGCTGTTCGGGCCGC[A/G]TGTTTTGCTTTTGTG | 54442 |
rs548868941 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708347 | TCACTCGACCTGCAC[A/G]GGCTCTGCCCGACAT | 54442 |
rs548902841 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703663 | CTCACGGCAGCCTTT[C/T]CACCTCAGGCGACTG | 54442 |
rs548958347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700593 | TCCTGGTGCTAGACA[G/T]ACACTGAGGGTGGGG | 54442 |
rs548974349 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2680568 | GAAGATGTTGTCATA[C/T]ACTTTTCCCCAGTTA | 54442 |
rs548995147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701062 | TGTCAGCAGCTCGGG[A/G]TCCGCGAACAGGGCT | 54442 |
rs549012769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706310 | TCTCTCCGGTCAGTG[C/T]GGCATGGCAGTGACC | 54442 |
rs549027844 | snp | G/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2693375 | GCCAGACTGAGGTCA[G/T]GAGTTCCTTCAAAGC | 54442 |
rs549156657 | snp | A/G | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2692583 | TCTTATGGACCCAGA[A/G]GGAAGGAAGTGCATA | 54442 |
rs549170236 | in-del | -/A | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708018 | ATAGACTCCCCAGCG[-/A]TTTTTCCTCTGGAAA | 54442 |
rs549176845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705409 | TGACTGGAGGGTGCC[C/T]GTGCCAGGCCAGGCT | 54442 |
rs549191173 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702196 | CCGTGTGCTCGTGCA[C/G]GTGTTCCGGGGATTT | 54442 |
rs549225639 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697849 | GGGTGGGTGTAAAGC[A/G]TGGATTCTTTGGTTT | 54442 |
rs549227342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705959 | TGGCCTGTCCGCTGC[A/G]CTACTTAGTTTTACA | 54442 |
rs549395572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693047 | CCCACGCAGATCCTC[C/T]TCCCGAGGCCCGGGA | 54442 |
rs549460360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705065 | GTGGGGGTTTGGGCC[C/T]GGGGCACCCGCCCAC | 54442 |
rs549575704 | snp | A/C | 1.6888e-05 | 0.00290581 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707383 | CCCGAGATGTAATGA[A/C]CTGCCATGTCCAGGA | 54442 |
rs549593089 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KCTD5 | GRCh38.p7 | 16:2685287 | AAAAAAATTAGCTGG[A/G]CATGGTGGCGCGTGC | 54442 |
rs549677705 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693478 | CCAAGACACGGCAGC[A/G]GCCTACCCCTGCCTG | 54442 |
rs549871958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705082 | GGGCACCCGCCCACC[C/T]GCACTGTCCTGACAG | 54442 |
rs549925334 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2682442 | CGCGTGACGCCGGGG[C/T]GGGCGCTCTACCAGG | 54442 |
rs549988369 | snp | C/G | 0.111224 | 0.207945 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688746 | GGCTGACCCTAGCAG[C/G]ACAGGCCCCCGCTGA | 54442 |
rs550008175 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702972 | GGCCTCATCTTTGTC[A/C/G]AGAGGAGGGTGTCCT | 54442 |
rs550037337 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681876 | CTCCCGAGTAGCTTG[C/G]ATTACCGGCGCCCAC | 54442 |
rs550101375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687139 | GCAAACCTGTGCTCA[C/T]CTCTTTATCAGGTGC | 54442 |
rs550261369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684461 | CAATATGGTGATGCC[C/T]GGTCTCTACTAAAAA | 54442 |
rs550324905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706985 | AGGGACCCGCGGGCC[A/G]AGTTGCGCTTCATGT | 54442 |
rs550342003 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687346 | TGGGCCCGCGGTCTT[C/T]GGCATTCTCGCCTCC | 54442 |
rs550421055 | snp | A/C | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2698450 | GGAAGAGGGGCGGCT[A/C]GCCACAGACACACCT | 54442 |
rs550422437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690094 | ATGGCGGAGAGCTGC[A/G]GCCGGAGTCTGGTGA | 54442 |
rs550500246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705101 | CTGTCCTGACAGCCT[A/G]TCTTCTCCCCCACTG | 54442 |
rs550549913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690343 | AACTGTCCTGCCCGG[C/T]CTACGTCCTGTGGCT | 54442 |
rs550561070 | snp | A/C | | | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2708976 | ATTTTATCAGCTTAC[A/C]GTTTAATGCCTAAGT | 54442 |
rs550593135 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2684770 | ACTCCATCACAAAAA[A/T]AAAAAAATAAAAAAA | 54442 |
rs550634917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699082 | GTCACTCAGGCATCC[C/T]TGGCATGAGTCACCA | 54442 |
rs550713409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696739 | TTCTGTTCTGGGCCT[C/T]TGGGCCTCGGCATCT | 54442 |
rs550828596 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KCTD5 | GRCh38.p7 | 16:2709085 | ATGCCACCCCGGGTC[A/G]CTCGGACCAAGGTGC | 54442 |
rs550959665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2706340 | CTCTGGGAGGCTGTG[C/G]CCGGCGAGGGCGTGG | 54442 |
rs551030228 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683334 | TCCTTTCCATCCACA[A/G]CACGCAGCACCCACT | 54442 |
rs551142757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2700100 | TTGGGAGTTCGGGTG[C/G]GGTGGGCAGAGGTGT | 54442 |
rs551169133 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681193 | TACAGACAAAGCAAA[A/C]ATTAAAAGAACTCAT | 54442 |
rs551226324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696368 | AGGTGGTCTGAGCGG[A/G]TGTGTGAGGCACATG | 54442 |
rs551247198 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2698308 | GGCCGGTCGGGGAGA[A/C]CCTGAGGTGGATGGC | 54442 |
rs551256271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704613 | AGCAAGGGCGGGCAC[C/T]TGGGCAGAGGCCGGG | 54442 |
rs551297904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699701 | GATTGCTTTGGGCCT[C/T]GTGCCCTGTGCTGAG | 54442 |
rs551352592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697136 | GTCTCTGAGGCCCTC[A/G]TCTCCTTGTCTCTAT | 54442 |
rs551391202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697524 | GAAGCGTCGGCCTCC[A/G]GGCTTGGAGGGAAAA | 54442 |
rs551391279 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690998 | CCTGGGCTGGGCACT[G/T]TCTGGGCCTGGGCTG | 54442 |
rs551397880 | snp | C/T | 0.000232643 | 0.0107827 | intron-variant | KCTD5 | GRCh38.p7 | 16:2702337 | GGGCTGCGTCTCAGG[C/T]TATGTCTCCTTGCAG | 54442 |
rs551474351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701673 | TGTGAGCCTCGTCCA[G/T]CTGCTTTTTGGCTTG | 54442 |
rs551728221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686986 | ATGGACTTTGTTTCA[C/T]GCTTCAGTTGAGGAT | 54442 |
rs551798924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2688404 | TACAGGCACGAGCCA[C/T]CATGTCTGGCTGATT | 54442 |
rs551855070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2701110 | GTGCTCTTCTGCCAC[C/T]GTCTTGTGACTTCTG | 54442 |
rs551906255 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2686639 | GGAGAAAACTGCACG[G/T]GAACTTTTGCCCTTT | 54442 |
rs552005897 | snp | C/T | 0.00166836 | 0.028834 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699180 | GCAGCCTGAGTCCTC[C/T]GTAGTGACTGTCCAG | 54442 |
rs552056733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2683713 | TATATTTATTCAAGG[C/T]AGTTCACAAGCCTTA | 54442 |
rs552111131 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD5 | GRCh38.p7 | 16:2699656 | AGCAGCTGTTCGGGC[C/T]GCGTGTTTTGCTTTT | 54442 |
rs552332773 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime | KCTD5 | GRCh38.p7 | 16:2682500 | GAGGACGCTATTAAA[A/C]GCCGGACGCTTCCGG | 54442 |
rs552356994 | snp | C/T | | | intron-variant | KCTD5 | GRCh38.p7 | 16:2687866 | AAGCCATCTCTCTCC[C/T]AGGACATGCTTGTTC | 54442 |
rs552686819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2687480 | GACTAGTCTTGGTTT[A/T]GAGCAGGAGTCAGAA | 54442 |
rs552721561 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2692894 | GGGGCCTTTCTGGGC[C/G]CCCAAGAGTGCAGGG | 54442 |
rs552738697 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2703136 | GACCCCTGCCTCGTT[G/T]GCTTTCAGGTTGGCC | 54442 |
rs552783415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2690670 | TCCTGGCCGCCTCTC[C/T]TCATCCCAGTCGTAG | 54442 |
rs552915811 | snp | A/G | 6.77759e-05 | 0.00582094 | utr-variant-3-prime | KCTD5 | GRCh38.p7 | 16:2707473 | CCTTTTTTGCCTCTG[A/G]GGTGGGTGGTGAGAG | 54442 |
rs552929340 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD5 | GRCh38.p7 | 16:2697156 | CTTGTCTCTATCCTG[C/T]GTGGCCCTGTCCCAT | 54442 |
rs552987383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2704878 | GGAGTGGGGCCAGAG[A/G]CCAGGCGCCTCTGGA | 54442 |
rs553012821 | in-del | -/CTTT | | | upstream-variant-2KB | KCTD5 | GRCh38.p7 | 16:2681742 | GCTTTATTACAAAAA[-/CTTT]CTTTTTTTTTTTTTG | 54442 |
rs553092834 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2693653 | AGTTGCAGGGCTGGG[G/T]TTGCCTCGTGTGTCT | 54442 |
rs553130775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD5 | GRCh38.p7 | 16:2696998 | AACGGGCGCTAGACA[C/T]AGACCAAGGCCCTGC | 54442 |
rs553275625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD5 | GRCh38.p7 | 16:2705125 | CCCACTGCGCGCTGC[A/G]CGCCGCCAGAGTGAC | 54442 |