SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1129700 | snp | A/G | 0.494013 | 0.0543839 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29906713 | GGCCCTTCTCCACCC[A/G]TCCCAACCCCATTGC | 253980 |
rs4076756 | snp | C/T | 0.121717 | 0.214577 | intron-variant, utr-variant-3-prime, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29919954 | AAGAAAAAATATTGG[C/T]GATATCTACATTGAC | 253980 |
rs4238958 | snp | A/G | 0.0236746 | 0.106192 | intron-variant, utr-variant-3-prime, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29919744 | TGTGTGTGTGTGTGT[A/G]TTTGCTTGCCAAAAT | 253980 |
rs4407079 | snp | C/T | 0.470034 | 0.11868 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29920578 | attcatgttctttac[C/T]agattttctgctttt | 253980 |
rs4420550 | snp | C/T | 0.494358 | 0.0528145 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29927499 | GCTGTTGGTGCCAGG[C/T]CAGCTCCTAGCAACA | 253980 |
rs4424923 | snp | A/G | 0.496034 | 0.0443518 | upstream-variant-2KB, intron-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29927972 | gcactttgggaggcc[A/G]aggtgggcatatcac | 253980 |
rs4548895 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29912189 | AGAGTGGCAGAGAGG[C/T]TGGCGGAGCTTGGAG | 253980 |
rs4609871 | snp | A/G | 0.494896 | 0.0502606 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29920743 | GCATGTCCTCATCAA[A/G]ACATGGCATCATCCA | 253980 |
rs4788189 | snp | C/T | 0.493247 | 0.0577133 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29909890 | gcctgaccaacatgg[C/T]gaagtctctactaaa | 253980 |
rs5816505 | in-del | -/A | 0.497867 | 0.0325897 | intron-variant, upstream-variant-2KB | KCTD13, LOC107984836 | GRCh38.p7 | 16:29925760 | GTTGGGGGTCTGGGG[-/A]TGGGGGCACGGTAGG | 253980 |
rs7184288 | snp | C/G | 0.490231 | 0.0692021 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923731 | ctgggcttggtggct[C/G]gtgccagctactcgg | 253980 |
rs7197342 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29917378 | TAggtcaggtatagc[A/G]gatcacacctgtaat | 253980 |
rs7201384 | snp | A/G | 0.495213 | 0.048687 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913584 | gggtggctccggcac[A/G]gggtctcttctgagg | 253980 |
rs8047140 | snp | C/T | 0.410399 | 0.191761 | intron-variant, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911667 | AGGACCTGCCTAGAG[C/T]GTCAGGGGTAAGAGG | 253980 |
rs8048433 | snp | C/T | 0.496681 | 0.0405994 | intron-variant, utr-variant-3-prime, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29920272 | gaggttgcagtgagg[C/T]aagatcgcgccactg | 253980 |
rs8050576 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29908471 | ctcactgcaacctcc[A/G]cttcccaagttcaag | 253980 |
rs8052502 | snp | C/T | 0.470327 | 0.118136 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29918407 | AACGTGAAATACATA[C/T]ATAATATTACCTAAA | 253980 |
rs8059619 | snp | C/T | 0.469937 | 0.118861 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914124 | cgtgagccacagcgc[C/T]gggcccctccattgt | 253980 |
rs9925913 | snp | C/G | 0 | 0 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29921479 | agcctggggtcaaat[C/G]tgagctctgctgctt | 253980 |
rs9928945 | snp | A/G | 0.00086512 | 0.0207801 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923403 | AGATGGCTTTGCTGC[A/G]GGACCTGGAGCTACT | 253980 |
rs9936474 | snp | C/T | 0.469937 | 0.118861 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29921370 | CACTGAGGAGTGTGC[C/T]GAGCTGCGTGAGGTG | 253980 |
rs10083738 | snp | A/G | 0.470424 | 0.117954 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29916381 | agtgtgaaccactgt[A/G]cccagccaatacttt | 253980 |
rs11150574 | snp | C/T | 0.469937 | 0.118861 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923498 | CTGGGCTCAAGTGAT[C/T]CTCCCATCTCGGCCT | 253980 |
rs11150575 | snp | C/G | 0.431916 | 0.171483 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923745 | TGGTGCCAGCTACTC[C/G]GGGGGGGGCGAGGCA | 253980 |
rs11644809 | snp | A/G | 0.497722 | 0.0336691 | intron-variant | KCTD13 | GRCh38.p7 | 16:29924184 | CATCTCAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 253980 |
rs11646118 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29915150 | gtcccacctcttcca[C/T]gaaagatgtttgcag | 253980 |
rs11647753 | snp | A/G | 0.498852 | 0.0239341 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29916794 | tggccctggcccaga[A/G]tctgtcatgaagctg | 253980 |
rs11649519 | snp | A/G | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29907524 | tggcgcagtgactca[A/G]gcctgtaatcccagc | 253980 |
rs11865766 | snp | A/C | | | intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29918732 | cacgatctcggctca[A/C]tgcaacctctgcctc | 253980 |
rs12232459 | snp | C/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914357 | ctcaaagtacagaat[C/T]tcatcatctcagtca | 253980 |
rs12444978 | snp | A/T | 0.469839 | 0.119042 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913101 | ACAGAGAATAATAAA[A/T]GTCTACAATTACTGA | 253980 |
rs12447999 | snp | G/T | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29908688 | catgcccggccTTtt[G/T]tttttttttttaatc | 253980 |
rs12448030 | snp | A/G | 0.126564 | 0.217402 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922223 | AAAAGTTTGAAAAAC[A/G]TGGATATTGTCCAAA | 253980 |
rs12596042 | snp | A/T | 0.470132 | 0.118498 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923433 | TAAATTAAAAAAAAA[A/T]TTTTGTAGAGATGGA | 253980 |
rs12716972 | snp | A/G | 0.495521 | 0.0471118 | intron-variant, upstream-variant-2KB | KCTD13, LOC107984836 | GRCh38.p7 | 16:29925333 | GGGAACACAGAGGCA[A/G]ACAAGATCTCCCAGC | 253980 |
rs12716973 | snp | A/G | 0.471388 | 0.116136 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926331 | GGCGTGTGGCCTGCG[A/G]GTTCCCCGGGCGGGT | 253980 |
rs12932403 | snp | A/G | 0.44651 | 0.154543 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922729 | GTTTAAAAAAAAAAA[A/G]GAATTAGAAAGCTCC | 253980 |
rs12933766 | snp | C/T | 0.494526 | 0.0520291 | intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29910690 | TGGCAACTATGGACC[C/T]CCTATACAGAAAAAT | 253980 |
rs12935265 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29919707 | AAAACAGATTATAAA[A/G]CATTTCATACAACAC | 253980 |
rs17853574 | snp | A/G | 0 | 0 | synonymous-codon, nc-transcript-variant, intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911065 | GTAGAAAGACCAGCA[A/G]CAGATCTCGTCCCCC | 253980 |
rs34090922 | in-del | -/C | 0.0592355 | 0.161582 | upstream-variant-2KB | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926252 | CGCAGCCCCGCCCCC[-/C]ATTCAGGGGCGGGGC | 253980 |
rs34173971 | in-del | -/C | | | intron-variant, upstream-variant-2KB | KCTD13, LOC107984836 | GRCh38.p7 | 16:29924984 | CACGCCTTTAATCCC[-/C]AGCACTTTGGGAGGC | 253980 |
rs35012369 | in-del | -/G | | | intron-variant, splice-donor-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911660 | CCCCTGACGCTCTAG[-/G]CAGGTCCTTTCTGCT | 253980 |
rs35278775 | in-del | -/T | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29907414 | GTTCACTGCTATTTT[-/T]GCAGTGCCTAGAACA | 253980 |
rs35345720 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922282 | AACAACTTTTGTCTC[A/T]GGGAATACTTACTGG | 253980 |
rs35566440 | in-del | -/GAAT | 0.304438 | 0.244001 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29909050 | AATGAATGAATGAAT[-/GAAT]CAGTGACCCAGCTTC | 253980 |
rs35691158 | snp | C/G | 0.444444 | 0.157135 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29909173 | AGGGGGTTTGCATCA[C/G]CAGCGAGGTGTTAGT | 253980 |
rs35756092 | in-del | -/A | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913121 | AAAAAAAAAAAAAAA[-/A]TGGCCTCAGTAATTG | 253980 |
rs56885319 | in-del | -/CA | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29919759 | ACACACACACACACA[-/CA]TACTCTCACACAGGA | 253980 |
rs57383025 | snp | C/T | 0.00496891 | 0.049596 | intron-variant | KCTD13 | GRCh38.p7 | 16:29923031 | GGGTGCTGCCTGAGG[C/T]GGCAGGGATGCAGAA | 253980 |
rs60476091 | snp | A/C | | | missense, nc-transcript-variant, intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911006 | TTCTCCGTAGCATAG[A/C]CAATGGAGGTGCAGC | 253980 |
rs62056408 | snp | A/T | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29912898 | GTTGAGTGAATGAAC[A/T]TCATTGGGTGGGATG | 253980 |
rs62056409 | snp | A/G | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29915135 | GGCTCTCCCTGAGTC[A/G]TCCCACCTCTTCCAT | 253980 |
rs62056410 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29915644 | AAGAAAAAAGAAAAT[A/C]TCTGCAAGGTAAGCC | 253980 |
rs71276820 | in-del | -/A | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913122 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 253980 |
rs71373213 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926610 | GGCCAAAGCGGCCGG[-/G]CGCTGTGGCTCACAC | 253980 |
rs71373214 | in-del | -/G | 0.5 | 0 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926612 | CAAAGCGGCCGGGCG[-/G]CTGTGGCTCACACCT | 253980 |
rs71389436 | snp | C/T | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914664 | TCTTTAACTCCTGAC[C/T]TCAGGTGATCCACTT | 253980 |
rs72170823 | in-del | -/A/AA/AAAAAAA | | | intron-variant | KCTD13 | GRCh38.p7 | 16:29924174 | GTGAAACTCCATCTC[-/A/AA/AAAAAAA]AAAAAAAAAGAAAAG | 253980 |
rs72228738 | in-del | -/TTCA | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29909051 | TCATTCATTCATTCA[-/TTCA]ATAAATGTTTCCTAG | 253980 |
rs72622531 | snp | A/G | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914583 | GGCTTGGTGGTGCGT[A/G]CCTGTAATCCCAGCT | 253980 |
rs72798147 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911737 | GCCCCCCGTGTGGCC[A/G]TGGCCCTCGCCTTGG | 253980 |
rs72798148 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29915231 | AAGCCGTCTTGTCCT[C/T]TTGCACTGGCTCTGT | 253980 |
rs72798151 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922569 | ACCCTTATGTCCTGG[C/T]TTCACTTTCCAAGCT | 253980 |
rs74017650 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29916645 | AAGGCTGGAGGACTG[C/G]TTGAGGTCAGGAGTT | 253980 |
rs74214105 | snp | G/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914551 | TCAAGTGATTCTTCT[G/T]CCTCAGCCTCCAGAG | 253980 |
rs74269399 | in-del | -/TTTG | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913141 | TTTTTTTTTTTTTTT[-/TTTG]AGACAGGGTCTTGCT | 253980 |
rs74579428 | snp | A/T | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29908701 | TTTTTTTTTTTTTTA[A/T]TCGTTGTTTGTTTGT | 253980 |
rs74859909 | snp | C/T | 0.0592355 | 0.161582 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29927100 | GAGAAGTGTTTTTAT[C/T]TGACCCGATCTGCAT | 253980 |
rs74900223 | in-del | -/AATA | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29910114 | AAAAAAAAAAAAAAA[-/AATA]GGCTGGGGGCAGTGG | 253980 |
rs75225650 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29905985 | CCTCCTCTCTACTGC[A/G/T]GGGGTGGGCGGGGGC | 253980 |
rs75365923 | snp | G/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914450 | CTTTTTTTTTTTTTT[G/T]TTTGAAATGGAGTCT | 253980 |
rs75546749 | snp | C/T | 0.126219 | 0.217206 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29910015 | GAGGCAGGAGAATCA[C/T]TTGAATCTGGGAGGC | 253980 |
rs75549506 | snp | A/T | 0.046775 | 0.145601 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922418 | ATAGAACAGAATAAC[A/T]GGCTTTATGTAAAAC | 253980 |
rs75599468 | snp | C/T | 0.122411 | 0.214991 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29921377 | GAGTGTGCTGAGCTG[C/T]GTGAGGTGCAGAGGG | 253980 |
rs75621288 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922146 | TATCTTTTTATAGAA[A/C]TGTTATTTCAGTTAT | 253980 |
rs75651136 | snp | C/G | 0.0146672 | 0.084371 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926119 | GGCCGGCCCCCAGCC[C/G]TTGGGCCAGACCGCT | 253980 |
rs75731600 | in-del | -/TTG | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914452 | TTTTTTTTTTTTTTT[-/TTG]AAATGGAGTCTTGCT | 253980 |
rs76093043 | snp | A/G | | | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29913378 | AAACACAACAGAGCG[A/G]TCAGAAACAGACCAC | 253980 |
rs76603667 | snp | C/T | 0.0287284 | 0.116357 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29921492 | ATCTGAGCTCTGCTG[C/T]TTCCCAGCTCTTTCA | 253980 |
rs77157526 | snp | G/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914452 | TTTTTTTTTTTTTTT[G/T]TGAAATGGAGTCTTG | 253980 |
rs78022435 | snp | A/G | 0.067446 | 0.170804 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29927555 | CAAAATAATTTCACA[A/G]AAAACATCAGACAAG | 253980 |
rs78082053 | snp | A/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29908699 | TTTTTTTTTTTTTTT[A/T]AATCGTTGTTTGTTT | 253980 |
rs78248865 | snp | C/T | 0.120674 | 0.21395 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29916391 | ACTGTGCCCAGCCAA[C/T]ACTTTTTAACACTCC | 253980 |
rs79019231 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29918217 | TGTGTGTCATTGATA[A/G]GTAACTGCCTTAATA | 253980 |
rs79442918 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922395 | AGGACATTTTTAACA[C/T]TGTAAAAATAGAACA | 253980 |
rs79465885 | snp | A/G | 0.122758 | 0.215196 | upstream-variant-2KB, nc-transcript-variant | KCTD13, LOC107984836 | GRCh38.p7 | 16:29926299 | AGTGGCCTCGCTGGG[A/G]GATCCCGTAGAGGTT | 253980 |
rs79656893 | snp | C/T | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914591 | ATTAGCGGGGGGTGG[C/T]GGTGCACGCCTGTAA | 253980 |
rs79786822 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29921678 | TAGTTTTAACATTAG[C/T]AAATTTAAAACTACA | 253980 |
rs79922206 | snp | A/C/G | 0.0240643 | 0.107019 | intron-variant, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911296 | TTTGGTGCTCAACAG[A/C/G]GAGCCTCCTCCACCC | 253980 |
rs79931750 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | KCTD13 | GRCh38.p7 | 16:29920793 | CACTGCTCATTATGA[G/T]GATAAAGTATTATAA | 253980 |
rs80273739 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KCTD13 | GRCh38.p7 | 16:29922580 | CTGGCTTCACTTTCC[A/G]AGCTCTGCTCCTCAG | 253980 |
rs111532054 | snp | A/G | 0 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29912502 | CTGGAGTGCAATGGC[A/G]CCATCTCGGCTCACT | 253980 |
rs111999248 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, utr-variant-3-prime, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29906014 | GCGGAGGATGGGAAC[C/T]GGCTAGTGAGCACTG | 253980 |
rs112012242 | snp | A/C | 0 | 0 | intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29910880 | ATCTGGCTCCTGCCT[A/C]CTGGTGGTGGGCTCC | 253980 |
rs112698693 | snp | C/T | 0.120674 | 0.21395 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29914527 | CACTGAAAACTCTGC[C/T]TCCCAGGTTCAAGTG | 253980 |
rs112724897 | snp | A/G | 0.5 | 0 | intron-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29907490 | CTCAGTCATACACTT[A/G]AGAAAATATAAACTA | 253980 |
rs113539656 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, nc-transcript-variant | KCTD13, ASPHD1 | GRCh38.p7 | 16:29911415 | ACCGGGAGCCAGGCC[A/G]CCTCCCCGGGGGTCC | 253980 |
rs113565760 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | KCTD13, ASPHD1 | GRCh38.p7 | 16:29918559 | CACTGCAACCTCTGC[C/T]TCCCAGGTTCATATA | 253980 |
rs113767385 | snp | A/C | 0.5 | 0 | intron-variant, synonymous-codon, nc-transcript-variant | KCTD13 | GRCh38.p7 | 16:29923154 | CTTGGGCAGCTCTCC[A/C]AGGAACATAGGCATG | 253980 |