SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs958579 | snp | C/T | 0.389152 | 0.207694 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441159 | CTCTGTTGTCTTTGT[C/T]GCATTCAACTTGGAT | 54793 |
rs965130 | snp | C/T | 0.498714 | 0.0253268 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430040 | GCCCCAGAAATCATT[C/T]TGAGCAGAAATAGAT | 54793 |
rs1506863 | snp | A/T | 0.470746 | 0.117351 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460308 | TAATGCTGGTATGTG[A/T]TGATCTGCCTCCTTG | 54793 |
rs1506871 | snp | C/G | 0.484209 | 0.0874434 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457055 | GAATTCGTATAAATT[C/G]GAGTTCTTGAGTTAT | 54793 |
rs1506872 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456933 | TGTTATCTAAAACGT[A/G]TGTTGTTACTCTAAG | 54793 |
rs1506873 | snp | A/C | 0.482234 | 0.0925596 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456876 | AATATTTCTCAAAAA[A/C]AAACTTCTGGTTGAC | 54793 |
rs1567120 | snp | A/C | 0.486855 | 0.0799975 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452728 | gtttattttctttat[A/C]ttttgttgttaaatt | 54793 |
rs1567121 | snp | C/T | 0.498714 | 0.0253268 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450282 | CAAGGGATAATTGGT[C/T]ACCTCTATTCACAGA | 54793 |
rs1812594 | snp | A/G | 0.318776 | 0.240354 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429881 | GATGCTGACACCACT[A/G]CACATGTCACAAAGT | 54793 |
rs1827957 | snp | C/T | 0.0524604 | 0.153226 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428755 | CAGCCACCAAAAAAA[C/T]AGACGTAAAAATAAA | 54793 |
rs2012592 | snp | A/G | 0.473064 | 0.112883 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436342 | CACTAATTTCTTAAT[A/G]TCTTTTTTAAGAATT | 54793 |
rs2048085 | snp | A/G | 0.486266 | 0.0817214 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436836 | AACAGATTAGAATAA[A/G]TAAATATACCAAGTC | 54793 |
rs2048086 | snp | C/T | 0.486266 | 0.0817214 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436831 | ATTAGAATAAGTAAA[C/T]ATACCAAGTCATGTA | 54793 |
rs2063064 | snp | C/T | 0.498774 | 0.02473 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447357 | cttggtcataaaggc[C/T]ggagtgcagtggtgc | 54793 |
rs2063065 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447226 | tttgtattttagtag[A/G]gatggggtttctcca | 54793 |
rs2063066 | snp | A/G | 0.486133 | 0.082104 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447182 | ggtctcaaactccag[A/G]ccttaagtgctctgc | 54793 |
rs2063067 | snp | C/G | 0.487621 | 0.0776941 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446913 | ATTCACAGCAGGACA[C/G]ATCAATTCATTGTCA | 54793 |
rs2063068 | snp | A/T | 0.486133 | 0.082104 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446014 | GGATTTTGGCAAGTG[A/T]TTACCTAGAATTTGC | 54793 |
rs2063069 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445897 | GCATAGTTCATATAT[A/G]GCTATGAGGAATTTC | 54793 |
rs2271112 | snp | A/G | 0.47117 | 0.116549 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439414 | CTTTATTATAATGGT[A/G]ACACAGGTGTCTGGG | 54793 |
rs2271113 | snp | G/T | 0.0008849 | 0.0210159 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436502 | AGGTTGTTTCAGAAT[G/T]ATTTTTGTTCTGATA | 54793 |
rs2271114 | snp | C/T | 0.00209145 | 0.0322699 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436337 | ATTTCTTAATGTCTT[C/T]TTTAAGAATTCTCAA | 54793 |
rs2321050 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428081 | TAGATCTAAAATCTG[C/T]AGTTTCTAAGCACAC | 54793 |
rs2321051 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428097 | AGTTTCTAAGCACAC[C/T]ATGTTTAGATCTTTC | 54793 |
rs2321052 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428164 | TACCTTTAAGTGAAT[A/G]AATACCACATTCTGT | 54793 |
rs2321053 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428574 | AAAATAAGGACACCA[A/G]GTCATTGGTAGGGAG | 54793 |
rs2321054 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428622 | GCTGCTGCAGAGAGA[G/T]AATGACTCAAGAAAA | 54793 |
rs2321055 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428677 | AAAAAACCACAAAAA[A/T]ATAAGTAAAAGAATC | 54793 |
rs2321056 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428711 | GGTGCTGACTGATTG[A/G]TAATTACATCTTGGA | 54793 |
rs2321057 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428751 | TGCCTTTATTTTTAC[G/T]TCTATTTTTTTGGTG | 54793 |
rs2321058 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428770 | ATTTTTTTGGTGGCT[A/G]TAATCAAATGTGTGT | 54793 |
rs2321059 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428775 | TTTGGTGGCTGTAAT[A/C]AAATGTGTGTTTAAA | 54793 |
rs2321060 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428802 | TAAAATTCCTCATTC[C/T]CCACTGTAGGGTTCT | 54793 |
rs2321061 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429064 | AGATAGAATTGCTTG[A/G]TCTGGTGTTGAGTGG | 54793 |
rs2874426 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428064 | ATTAATGCAGTATAC[A/G]TTAGATCTAAAATCT | 54793 |
rs2874427 | snp | A/C | 0.154525 | 0.231051 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428663 | ATTTGTTTAAAAAAA[A/C]AAAACCACAAAAAAA | 54793 |
rs2874428 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429261 | AATTTAGCTACTGTT[C/T]TGTCCTAAAAAGTAA | 54793 |
rs3057669 | in-del | -/TACAG | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428197 | TTCCTGAAAATATAG[-/TACAG]AGTGAAATGATTTAA | 54793 |
rs3057725 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428752 | CCTTTATTTTTACGT[-/TA]CTATTTTTTTGGTGG | 54793 |
rs3057729 | in-del | -/CCTAA | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429269 | ACTGTTCTGTCCTAA[-/CCTAA]AAAGTAAACATTATA | 54793 |
rs3180395 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429074 | TAGGCAAGTTCCACT[C/T]AACACCAGATCAAGC | 54793 |
rs3215161 | in-del | -/T | 0.271432 | 0.24908 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436796 | ATGTACATTTTTTTT[-/T]ACCAAGTTAAAGTAA | 54793 |
rs3215162 | in-del | -/A | 0.487495 | 0.0780784 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433272 | ACTGTAAAGGAAAAA[-/A]GCCCTGGAAAATAAT | 54793 |
rs3750198 | snp | A/G | 0.154993 | 0.231244 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438950 | TACATTCTTAATTCA[A/G]TTTTTAAAAAAGGAA | 54793 |
rs3812421 | snp | C/T | 0.482683 | 0.0914256 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459273 | CCTGGACTCACAGCC[C/T]GCGCTGATCCTGGCC | 54793 |
rs3812422 | snp | A/C | 0.482459 | 0.0919928 | utr-variant-5-prime, upstream-variant-2KB, splice-donor-variant, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459145 | TCACTCCGCCACCTC[A/C]CCCTTCTCCAGTCCG | 54793 |
rs3812423 | snp | C/G | 0.486067 | 0.0822953 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441194 | CTTAACTTTCATCTG[C/G]AGTCCTTTTTTTTTT | 54793 |
rs3967544 | snp | A/G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429117 | GAGAAATTCTCATTT[A/G/T]TAAGTGTTGTAGTGA | 54793 |
rs3967545 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429155 | GTTATTCCTCCATCC[A/G]GAGTTACACTGTACC | 54793 |
rs3967546 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429187 | TTGGAATGACAGTGA[A/T]GTACAATGATGTCTT | 54793 |
rs3967547 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429335 | CTCACCATATTCATA[C/T]GGTGTGACAGGTATT | 54793 |
rs3967548 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429339 | CCATATTCATACGGT[A/G]TGACAGGTATTTAAA | 54793 |
rs4056563 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429017 | CTATGCTTGTGATGA[C/T]TGTATGAGAAAACTA | 54793 |
rs4056564 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429033 | TGTATGAGAAAACTA[A/G]GCTAATAGTGTAAAT | 54793 |
rs4056570 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428169 | TTAAGTGAATGAATA[A/C]CACATTCTGTAATTC | 54793 |
rs4056571 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428178 | TGAATACCACATTCT[A/G]TAATTCCTGAAAATA | 54793 |
rs4056572 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428210 | AGTACAGAGTGAAAT[A/G]ATTTAAATATAATTT | 54793 |
rs4056573 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428226 | ATTTAAATATAATTT[A/G]GGCACATATTGATTA | 54793 |
rs4056574 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428256 | ATGAAAATAGATTAT[C/T]TCTCAATACAATACT | 54793 |
rs4056575 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428665 | TTGTTTAAAAAAAAA[-/AA]NACCACAAAAAAATA | 54793 |
rs4056576 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428667 | TTTAAAAAAAAAAAN[-/AC]CACAAAAAAATAAGT | 54793 |
rs4871941 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440260 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 54793 |
rs4871942 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453041 | ATCAATTTGAGATAC[C/T]GTATGTCCCGAAGCT | 54793 |
rs4872311 | snp | C/G | 0.498673 | 0.0257246 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431362 | TTTGACAGATGTACA[C/G]AACAGTGTAACCACC | 54793 |
rs4872312 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452863 | tggaagagaattata[C/T]tgaacgaaaaaagca | 54793 |
rs4872313 | snp | A/G | 0.495927 | 0.0449436 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457344 | TAGGTATCATTTAGC[A/G]ACGCAATAAATGTCT | 54793 |
rs6557842 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437263 | TTATAAAAGAGGTTC[C/T]TGTGGGCCACGCTCT | 54793 |
rs6987936 | snp | A/T | 0.081446 | 0.184634 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460175 | AGTCCTGAATAAGGT[A/T]CGTGATCGAATCACG | 54793 |
rs6991793 | snp | C/T | 0.485255 | 0.0845871 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460056 | TATCAAAATATTTCA[C/T]GTACCCCATAAATTA | 54793 |
rs7009732 | snp | C/G | 0.498734 | 0.0251279 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430509 | tcatgagaatctaat[C/G]cctgatgatctgtca | 54793 |
rs7013282 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440090 | TTGAGAAGGAGTCTC[A/G]CTCTGTCACCCAGGC | 54793 |
rs7017457 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440354 | TGAGCCACCGCGCCC[A/G]GCCAAAAGCATGTTC | 54793 |
rs7459536 | snp | C/G | 0.0807149 | 0.183963 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444842 | GCTGCACATAACCCA[C/G]AGTTCTGGACAATCA | 54793 |
rs7459786 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445029 | CTAAGAAGCAGAGTT[C/T]GTGTTTGTTAAGAAG | 54793 |
rs7817173 | snp | C/T | 0.490782 | 0.0672626 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450766 | CAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 54793 |
rs7819740 | snp | A/G | 0.490618 | 0.0678448 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454518 | GATGTGCAAGTCCCC[A/G]TTTCAATTTCCTTAA | 54793 |
rs7829415 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449209 | GAAGGTGCTGTGAAA[A/G]GAGGGTAAGAAGCAC | 54793 |
rs7833509 | snp | G/T | 0.0252325 | 0.109451 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459229 | GCGGGCGGAGGAGGC[G/T]GGTGGAGGAGGCTGC | 54793 |
rs7835442 | snp | G/T | 0.487368 | 0.0784625 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454500 | AGCCACACACTGCAT[G/T]CAGATGTGCAAGTCC | 54793 |
rs7839773 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451727 | GGCTAGTTTTAATTT[A/G]CCTTTAAACACCATT | 54793 |
rs7840399 | snp | C/T | 0.388587 | 0.208071 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430898 | gctggagtgcaatct[C/T]ggctcactgcaacct | 54793 |
rs7841309 | snp | A/C | 0.0588605 | 0.161139 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448330 | catgaaagtacccaa[A/C]acaggcaaattcata | 54793 |
rs7842899 | snp | A/C | 0.486266 | 0.0817214 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434656 | ACAGCTTCATGGAAA[A/C]ATAAGCTGCAGCTAA | 54793 |
rs7844851 | snp | C/T | 0.498794 | 0.0245311 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446708 | AGTAAGTCCCTATTA[C/T]GTTGTCCTTTTATTA | 54793 |
rs9314302 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440966 | AGCCATCCATAGATA[C/T]TGACTTCATTGCTTA | 54793 |
rs9314303 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444141 | AAATTTACTTTAACA[C/T]ACCCAATGCAGAATC | 54793 |
rs10099739 | snp | A/C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431329 | AAAGCCCCAAAGGta[A/C/G]gtatataatacagtg | 54793 |
rs10108541 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441935 | cttgaacccaggagg[C/T]tgaagctgtagtgag | 54793 |
rs10503770 | snp | A/G | 0.487495 | 0.0780784 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445411 | TTGTATATCATTATA[A/G]GTTAAAGCATCATTA | 54793 |
rs10503771 | snp | C/T | 0.147321 | 0.227941 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446504 | AGGTGTGTTAAATAG[C/T]GCTCCAGTTGTGAAG | 54793 |
rs11135864 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450002 | TCAAATGTGACCAGA[C/T]GATAGAAAAAAACCA | 54793 |
rs11135865 | snp | A/G | 0.269809 | 0.249214 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452759 | aacctaatgtccact[A/G]acaggaatatcatgg | 54793 |
rs11135866 | snp | A/C | 0.0829908 | 0.186358 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455115 | ctgtaatcccagcta[A/C]gcaagaggctgagtt | 54793 |
rs11309645 | in-del | -/T | 0.490943 | 0.0666801 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434442 | TTTTTGACAAACATC[-/T]TTTTTTTTTTGTCCT | 54793 |
rs11419162 | in-del | -/A | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450751 | CCGCCTCAGCCTCCC[-/A]AAGTGCTGGGATTAC | 54793 |
rs11775241 | snp | A/G | 0.48546 | 0.0840147 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459906 | TTGCTAGCACAACAG[A/G]GTGGCGGTCCATAAT | 54793 |
rs11775249 | snp | A/G | 0.485392 | 0.0842056 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459945 | GCATTTAAACATAAC[A/G]AAGTATAATTGGATT | 54793 |
rs11776825 | snp | C/G | 0.487495 | 0.0780784 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449038 | ATTCCTGGGACAAAG[C/G]GAAGCGAAATACAGT | 54793 |
rs11778731 | snp | C/T | 0.446118 | 0.155041 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451000 | GTCAATTAGAGAAAA[C/T]AGAATTAAAATTAAT | 54793 |
rs11780132 | snp | A/G | 0.446641 | 0.154377 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448293 | cagtcacaaaaggat[A/G]aatattctatgatac | 54793 |
rs11781066 | snp | C/T | 0.446641 | 0.154377 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449005 | CACAGTGAGGTATTC[C/T]GTAATTGCATTATAC | 54793 |
rs11781868 | snp | C/T | 0.446249 | 0.154875 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449475 | GCTTAATACTTAATG[C/T]AATATTATAGCTTAA | 54793 |
rs11782310 | snp | C/T | 0.396909 | 0.202282 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444963 | AATTATAACCTTCCA[C/T]TGTAGACGTTTTTAT | 54793 |
rs11782643 | snp | C/G | 0.416218 | 0.186739 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455058 | TGGTGAAAACCGTCT[C/G]TACTAAAAATACAAA | 54793 |
rs11785124 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453614 | gccagagatcatgcc[A/C]ctgcactccaacctg | 54793 |
rs11786622 | snp | G/T | 0.45574 | 0.142025 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460098 | TATACCCACAGAAAT[G/T]AAAATAAAAAATGAA | 54793 |
rs11787383 | snp | G/T | 0.4862 | 0.0819127 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447390 | AGGCTCTGTCTCCCC[G/T]CTAAAAAAAGAAAAA | 54793 |
rs11984651 | snp | C/T | 0.485933 | 0.0826777 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455744 | CAATGACAACCAATC[C/T]GTGAAGAAGACACTA | 54793 |
rs11985969 | snp | A/G | 0.409212 | 0.192748 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454261 | TGAAAACACGGTACA[A/G]AATGAAAGTATTTCC | 54793 |
rs11987149 | snp | A/G | 0.485866 | 0.0828688 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455703 | AAATCTTAATGTGCC[A/G]GTTGTAAGCTTCCAT | 54793 |
rs11987153 | snp | A/G | 0.485933 | 0.0826777 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455745 | AATGACAACCAATCT[A/G]TGAAGAAGACACTAT | 54793 |
rs11995050 | snp | A/C | 0.291493 | 0.246533 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452526 | AAATTAAAAATGTAC[A/C]TTCCTACCCCACCCC | 54793 |
rs11998592 | snp | A/G | 0.486133 | 0.082104 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447592 | TGGAAAAAGCTGCTC[A/G]ATAACATACGAGTGT | 54793 |
rs13253805 | snp | A/G | 0.107341 | 0.205301 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453526 | GGTATGGTGGCGGGC[A/G]CCTGTAATCCCACCT | 54793 |
rs13262990 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450767 | aagtgctgggattac[A/G]ggcatgagccaccac | 54793 |
rs13272506 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437510 | ggtgaaaccctgtct[C/T]tactaaaaatacaaa | 54793 |
rs13273546 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437512 | tgaaaccctgtctct[A/T]ctaaaaatacaaaaa | 54793 |
rs13273899 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437660 | tccagcctgggtgac[A/C]cagcaagactccatc | 54793 |
rs13273930 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437692 | caaaacaaaaaaaat[A/C]caaatattagctggg | 54793 |
rs13274180 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437763 | tgaggcaggagaatc[A/C]cttgaacccaggagg | 54793 |
rs13274455 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437848 | gcgagaccctgtctc[A/C]aaaaaaaaaaaaaaa | 54793 |
rs13277090 | snp | C/T | 0.498754 | 0.0249289 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455940 | TGACCTCCAATAAAT[C/T]GTCTTGGACACTGTC | 54793 |
rs13438986 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437472 | ttgaggtcaggagtt[C/G/T]gagaccagcctggcc | 54793 |
rs17053653 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431743 | TGCTACTCTGCTACC[A/G]AGAGCTATCAAGATA | 54793 |
rs17053655 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438009 | GTTTGGATGGAAACT[C/G]TACTAACTGAAAACA | 54793 |
rs17053658 | snp | A/C | 0.105569 | 0.204058 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438748 | TGATGTAGATAGGGT[A/C]AAGAGTGCTTTTAAC | 54793 |
rs17053668 | snp | A/G | 0.486133 | 0.082104 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441379 | ATGAGCAATACAAAA[A/G]GACTGATCAAATGTT | 54793 |
rs17053694 | snp | C/T | 0.388021 | 0.208447 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451201 | TATGCAAAAACTCTG[C/T]ATTTTAAACTAATTA | 54793 |
rs17053696 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451596 | GTCTATTAAAGTTCA[C/T]GATGTCTGTATTATA | 54793 |
rs17053711 | snp | A/G | 0.378765 | 0.214288 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453753 | CAGGAGTACAGGAAC[A/G]TGGATAAACACATTA | 54793 |
rs17053712 | snp | A/G | 0.485731 | 0.0832509 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453794 | AACATGCTACTTCTT[A/G]GGTTATCTGGCAGAT | 54793 |
rs17053728 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458958 | GGCGGAGTTAAAGCG[C/T]TAAGAGAAGCGTTAC | 54793 |
rs17061024 | snp | A/T | 0.143284 | 0.226079 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429748 | TAAATGTTTTTTTTT[A/T]AAATTTCCTTACAGT | 54793 |
rs17201702 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441223 | AGAGGTTTAATAGAC[C/G]AGAATATATCAGAAA | 54793 |
rs17202453 | snp | C/T | 0.105214 | 0.203807 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456078 | TTCCTGGCGAGCATA[C/T]AACACAGCACCTTGG | 54793 |
rs28411311 | snp | C/T | 0.00347825 | 0.0415575 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432576 | ATTTTTTAAGGTAGC[C/T]ACTCTCAGGTTAATT | 54793 |
rs28470827 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447164 | TTTGTGAGGCTGAGA[C/T]GGGCAGAGCACTTAA | 54793 |
rs28662100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439744 | AGAGTATACTCGATC[A/C]CAGCTGCTCTCTCAA | 54793 |
rs34212446 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435312 | GCTCTTTGAGACTGT[-/G]TCAATAGACTAAACA | 54793 |
rs34288571 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454748 | TGGTAACATACTTTT[-/T]GGGCATGTACTCAAA | 54793 |
rs34334249 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431448 | TTCCACTTAAGTCCC[-/C]TGGATATGATAGGGG | 54793 |
rs34393437 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452990 | GGGCAATATAGGAAG[-/C]ACATTGTCTCCACAA | 54793 |
rs34459715 | in-del | -/A | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457681 | GCCCCCATTTTAAAA[-/A]TCCTGTCTGCGACCT | 54793 |
rs34637435 | in-del | -/G | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457525 | GACTGTCAAATCGAT[-/G]CCCTTTTGGGTCTGC | 54793 |
rs34836158 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438320 | TTTTTTTTTTTTTTT[-/T]GCAATAGGTACATGT | 54793 |
rs34912773 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454999 | GGAAGCCAAGGCAGG[-/G]TGGATCACATGAGGT | 54793 |
rs35307226 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454550 | CCAACTCTTACAGGG[-/G]AATATTAAAAAGAAT | 54793 |
rs35429268 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455744 | CAATGACAACCAATC[CA/TG]TGAAGAAGACACTAT | 54793 |
rs35596642 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434478 | AAACAAAGATGCCTC[-/C]TCGACATTTCACTAT | 54793 |
rs35972686 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443353 | TAAAATCCAACAAGG[-/G]TTTGTTAAAAAGACC | 54793 |
rs55994273 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430844 | ACACACACACACACA[A/T]TTTTTTTTTTGAAAC | 54793 |
rs56241318 | snp | C/T | 0.487241 | 0.0788465 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430495 | AGGTGGGGTACTCCT[C/T]ATGAGAATCTAATGC | 54793 |
rs56385545 | snp | A/C | 0.4862 | 0.0819127 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442628 | ACAAGTTTCAGATAA[A/C]CACTGGAAACATAAC | 54793 |
rs57227987 | in-del | -/G | 0.446641 | 0.154377 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449567 | ACTTGGTTTTTCTGT[-/G]GGTCTATTGTCTTCC | 54793 |
rs57257880 | in-del | -/TT | 0.712922 | 0.117993 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444243 | TTTTTTTTTTTTTTT[-/TT]GGCAGATAAAATTGG | 54793 |
rs59540797 | in-del | -/A | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437881 | AAAAAAAAAAAAAAA[-/A]TCTGGATTTGAATCC | 54793 |
rs59794332 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440076 | TTTTTTTTTTTTTTT[-/T]GAGAAGGAGTCTCAC | 54793 |
rs61100218 | in-del | -/A | 0.4862 | 0.0819127 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439227 | TAAAATCTTAAACTT[-/A]ACAAAAATGTGAGTA | 54793 |
rs61574438 | in-del | -/AATTTACAA | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427383 | TTCATAAGAATAATT[-/AATTTACAA]CATTTTCTACCAGAA | 54793 |
rs61648191 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437063 | AGTTATTTGGGAAGA[-/A]TAATACAATCTTTTC | 54793 |
rs62502020 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428452 | AAGATATGTCATTCT[A/C]CCAAAGGAGACACAG | 54793 |
rs62502021 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441174 | AACAAAGACAACAGA[A/G/T]ACAAAAAAAAAAAAG | 54793 |
rs62502022 | snp | A/G | 0.0252325 | 0.109451 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458321 | CCTTTTTCTCCTCCC[A/G]CCCTTCCCCTCCCTC | 54793 |
rs66596013 | in-del | -/A | 0.486133 | 0.082104 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443471 | ATAACAATAAAAAAA[-/A]CCTTAATTGATCATT | 54793 |
rs66649651 | snp | C/G | 0.485664 | 0.0834419 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459808 | AATGGTTAGCACAGG[C/G]TGGGAAGTGTATTGG | 54793 |
rs67144712 | snp | A/G | 0.483126 | 0.0902898 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458743 | ACGAGGGCGGGGTCT[A/G]GGGAAAGGAGGTGGA | 54793 |
rs67827926 | in-del | -/A | 0.487432 | 0.0782705 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443241 | TTCCCACTAAAAAAA[-/A]TCAAGGCTTGTTGGA | 54793 |
rs67882048 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449845 | AAAAAAAAAATGAAG[-/A]AAAAAAAACACAACT | 54793 |
rs71517819 | snp | C/T | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444475 | AAAGAAGCTAAGTTT[C/T]CAATGCTTTGTTTAA | 54793 |
rs73220005 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432312 | ACATTAGATAACACA[A/T]CTATCAAACTTATTT | 54793 |
rs73220007 | snp | C/T | 0.490727 | 0.0674567 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434181 | CTCAGCTCACTGCAA[C/T]CTCTGCCTCCCAAGT | 54793 |
rs73220009 | snp | A/C | 0.153665 | 0.230694 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441458 | TGCCAGAAATACCCA[A/C]AAAATAGATCAAAAT | 54793 |
rs73220072 | snp | A/T | 0.155325 | 0.23138 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445927 | CAGAAAGACTATCAG[A/T]ATACTGAAATGTACT | 54793 |
rs73220076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450295 | GTGACCAATTATCCC[C/T]TGGTAAAGCTGATAA | 54793 |
rs73220077 | snp | A/T | 0.44651 | 0.154543 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452264 | AAAAAAGAAAATTTT[A/T]AAATGGAAAATACTG | 54793 |
rs73220080 | snp | G/T | 0.483126 | 0.0902898 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458711 | CACCCTCTAGTTTAG[G/T]TAGCGCTTATCTGCA | 54793 |
rs73220081 | snp | A/C | 0.483126 | 0.0902898 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458715 | CTCTAGTTTAGGTAG[A/C]GCTTATCTGCATACG | 54793 |
rs73220082 | snp | G/T | 0.45645 | 0.140991 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459782 | TTAAAAGTACGCGCT[G/T]AGAGTAAAAGAATGG | 54793 |
rs73220083 | snp | A/T | 0.485528 | 0.0838238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459785 | AAAGTACGCGCTTAG[A/T]GTAAAAGAATGGTTA | 54793 |
rs73549218 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433105 | CCAACTAAAACCTTA[C/T]TAAATATTTGAGGTT | 54793 |
rs73549259 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448608 | CACACAGCAGGCTTG[A/C]CATAAATAATTAAAG | 54793 |
rs73549278 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452439 | ATTACAACTATGTGT[C/G]TATACCTTAGAGTGG | 54793 |
rs73549284 | snp | C/T | 0.0112041 | 0.0740036 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452914 | GCTCATGCCTGTAGT[C/T]GCAGCACCTTGGGAG | 54793 |
rs74703856 | snp | A/C | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452226 | TAATTTAAAAAAAAG[A/C]TGAGATAATTAACTC | 54793 |
rs75302826 | snp | A/T | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437882 | AAAAAAAAAAAAAAA[A/T]CTGGATTTGAATCCC | 54793 |
rs75418510 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448400 | GGAATGGAGACTTAT[A/T]TCTTAATGGTTACAA | 54793 |
rs75435960 | snp | A/G | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441188 | AGACAAAAAAAAAAA[A/G]GGACTGCAGATGAAA | 54793 |
rs75450002 | snp | C/G | 0.104149 | 0.203046 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455198 | CCACTTCACTCCAGC[C/G]TGGGTGGAAGAGCAA | 54793 |
rs75499878 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456547 | TATCTAGTACTCTCC[A/G]GTTTGGATTTTTACG | 54793 |
rs75655812 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459829 | AGTGTATTGGGGATG[A/G]ATGGGAAGGAAGTGG | 54793 |
rs75776956 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441670 | ACAATGACTTAAGGG[A/G]AAGAAAAGGTAAAAA | 54793 |
rs75975157 | in-del | -/TT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434451 | AACATCTTTTTTTTT[-/TT]GTCCTTAACACAAAC | 54793 |
rs76106189 | snp | A/G | 0.0228947 | 0.104514 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459729 | TGCTTTGGTGCCTGA[A/G]CAGCAGTTTTCTCCA | 54793 |
rs76289577 | snp | A/C/G | 0.128288 | 0.218372 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449837 | AAAAAAAAAATGAAG[A/C/G]AAAAAAAACACAACT | 54793 |
rs76295863 | snp | A/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428756 | TTATTTTTACGTCTA[A/T]TTTTTTGGTGGCTGT | 54793 |
rs76483978 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444943 | CTTATAGCTCAGAAG[C/G]CTTCAATTATAACCT | 54793 |
rs76488565 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431316 | TGCCCTTCTTTTTAA[A/G]GCCCCAAAGGTACGT | 54793 |
rs76861435 | snp | C/G | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455658 | TCACTTGGCATTTTG[C/G]TGAGGGTTAATTTGG | 54793 |
rs76875120 | snp | C/T | 0.14665 | 0.227637 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443349 | AGCCATAAAATCCAA[C/T]AAGGTTTGTTAAAAA | 54793 |
rs76983709 | snp | A/G | 0.105214 | 0.203807 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443731 | ACTTAAATATTCAGA[A/G]TGTGGACTGTATGGA | 54793 |
rs77119803 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432006 | TATAGAACATGTCCC[C/T]CCTGCACAAAGTGCT | 54793 |
rs77180072 | snp | A/G | 0.14665 | 0.227637 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434386 | CATGATCCACCACAC[A/G]CAGCCAAGAGTTTTA | 54793 |
rs78018397 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437342 | GGATACGTTTCCAAT[C/T]CTAGGTTTAGAATTA | 54793 |
rs78332134 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438663 | GAGGCCTATTAGCTT[C/T]CAAATATGCAACCAG | 54793 |
rs78413665 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458584 | CTCTGGCTAACCTAG[C/T]CGGGACGGAGGGAGG | 54793 |
rs78610578 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446432 | GGTGCCTAATATTGC[C/T]GACTCCTCAACTAGA | 54793 |
rs78776274 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450540 | AAGCAGTCTGGGCAT[G/T]GTGGCTCAAGCCTGT | 54793 |
rs78812200 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448969 | GTCCCCCATATTTCC[C/T]ATGATTGTTCACCTC | 54793 |
rs79365950 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430146 | GATGTTCTTCTATCT[G/T]TATTTGTTACCTCTA | 54793 |
rs79392441 | snp | A/G | 0.00125045 | 0.0249732 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440685 | GGATCTAGAGATGAC[A/G]TGTAGAAAATAATAC | 54793 |
rs79469157 | snp | G/T | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444259 | TTTTTTTTTTTTTTT[G/T]GGCAGATAAAATTGG | 54793 |
rs79835432 | snp | A/G | 0.105569 | 0.204058 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452903 | CTGGCATGATGGCTC[A/G]TGCCTGTAGTCGCAG | 54793 |
rs80350360 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436805 | CTTGGTAAAAAAAAA[C/T]GTACATCCTTTACAT | 54793 |
rs111432781 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430676 | ACAATAAATGTAACG[C/T]GCTTGAATCATCCCA | 54793 |
rs111685697 | snp | C/T | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434920 | AAAACGCCACTGAGA[C/T]GTTAACTTCCACAAA | 54793 |
rs111952768 | snp | G/T | 0.00930731 | 0.0675798 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460208 | CATCTTGCTGGTGGG[G/T]TTATTTTTCATTGTT | 54793 |
rs112379876 | snp | C/T | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438148 | TGGTTTGCAGATGTG[C/T]GACACAGCATGGATA | 54793 |
rs112480129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434989 | TACTTCTTGAGCAGT[A/G]ACATTTTCCCATTCC | 54793 |
rs112486802 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460164 | TATTACAATTCAGTC[C/T]TGAATAAGGTACGTG | 54793 |
rs112765525 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458700 | CTGAGCAGGCGCACC[C/T]TCTAGTTTAGGTAGC | 54793 |
rs113090690 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430440 | ATTAGATTCGCACAG[A/G]AGCGTGAACCCTATT | 54793 |
rs113104012 | snp | C/T | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432759 | TAATCTAAAATCTTG[C/T]CTCTCAACGAACTTA | 54793 |
rs113250379 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451980 | CCTGGATCCTAAAGG[C/T]CCAATAAAAAAATTA | 54793 |
rs113277158 | snp | A/G | 0.5 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439029 | GAATATAAAGTTGAT[A/G]CGTATGGCTTACATA | 54793 |
rs113320920 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444213 | AATGTTTAAGCTTAA[C/T]AGCCCCATTTAAAAT | 54793 |
rs113821011 | in-del | -/TGAA | 0.043167 | 0.140428 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454339 | TTACTAAGTGTTCAC[-/TGAA]TGAATGAATGAATGA | 54793 |
rs113931050 | snp | C/G | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458040 | TGAGGGTCGGGAGGA[C/G]GCCGCGGGGACCCTG | 54793 |
rs114285284 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430677 | CAATAAATGTAACGC[A/G]CTTGAATCATCCCAA | 54793 |
rs114292815 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456461 | AATCAACTGAAGGGA[C/G]AGAAAACACTGCCAA | 54793 |
rs114628019 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454497 | AGAAGCCACACACTG[C/T]ATGCAGATGTGCAAG | 54793 |
rs114711263 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455485 | AAACTCAGCACTGTT[C/T]CAACTTCTCAGGTCC | 54793 |
rs114732115 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455449 | GCAATTAATAAATAG[A/G]ACTTCAAATATTCTT | 54793 |
rs114873608 | snp | C/T | 0.00930212 | 0.0675613 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460424 | TGGGAAGATTGTGAC[C/T]CCTCAGAAGCATGCC | 54793 |
rs114971443 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442669 | GAGGTAAGTGTACGC[C/T]TGAAGAAGTAAAACT | 54793 |
rs115146877 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430721 | CTCTGATCTGTGAAA[A/G]TATTTTCTTCCACAA | 54793 |
rs115168028 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431921 | AAATCAATTTCTCAT[C/T]TGCACTAGCCAAATC | 54793 |
rs115231612 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434506 | TATTTAAAGATTAGG[G/T]CCTTCAAACGTTTTT | 54793 |
rs115511370 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430929 | CCACCTCCAGGATTC[A/G]AGCTATTCTCCTGCC | 54793 |
rs115532504 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442702 | ATGAGTGTATAAAGG[A/G]AGACACTATAATATA | 54793 |
rs115878656 | snp | C/G | 0.106633 | 0.204807 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431196 | AACAACAAAAGGAAT[C/G]AGATGGGGGGAAGAC | 54793 |
rs115922459 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438275 | TTAGTTATAAAGTTA[C/T]AGAACTAGCTAAAAG | 54793 |
rs116127012 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449276 | TTGCCATCATACAAA[G/T]AATTTTCTAAATCTT | 54793 |
rs116161967 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444855 | CAGAGTTCTGGACAA[C/T]CAGTGCACATCCTCT | 54793 |
rs116408703 | snp | A/C | 0.0287284 | 0.116357 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450015 | GATGATAGAAAAAAA[A/C]CACACATACTGCTTG | 54793 |
rs116533229 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433691 | GCATGCTCATTTTAC[A/G]TGAAACATAACGGTT | 54793 |
rs116562814 | snp | A/G | 0.0494327 | 0.149241 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457534 | AATCGATCCCTTTTG[A/G]GTCTGCTGTACCCGT | 54793 |
rs116595114 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455565 | AGTGGCAGCTTCTGC[C/T]ATTTCCTCATTGTTT | 54793 |
rs116666017 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433598 | TTTTCTAATTAAATA[C/T]AGTAAGAACTGGGAA | 54793 |
rs116836340 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432073 | CAAGTCTGCTAGCTA[A/C]ACTGGCAAATTAAGA | 54793 |
rs117154382 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451224 | ACTAATTAGAAACCA[A/G]GTTTTAAAATATATA | 54793 |
rs117216297 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433577 | TTTTCTGTTTACAAT[A/G]AAGGCTTTTCTAATT | 54793 |
rs117618014 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443485 | ATAAAAAAACCTTAA[C/T]TGATCATTTTTTATT | 54793 |
rs117905169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449315 | CTCTTATTTACCTCT[G/T]GCTCTTACATCTCAG | 54793 |
rs117922985 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451512 | CTGATGTTTCCATGT[C/T]ACTGGGATTATCTAC | 54793 |
rs118189496 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457592 | TAATAAAAAGAGTAC[A/G]GAGAAGTTTGGCGGC | 54793 |
rs138059151 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438039 | AATGCTTTATAAAAT[A/G]AATCCAGCAGAGAGC | 54793 |
rs138225083 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450179 | CAAAAACAATTTACC[A/G]TATCACTAAATATTT | 54793 |
rs138593635 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437280 | GTGGGCCACGCTCTC[A/C]ATTTGCCAAGGTCTA | 54793 |
rs138870707 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459703 | AAAGCCATGGCTTAT[C/T]CTTTGGGGTCTGCTT | 54793 |
rs138871917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448776 | AAAAATTAGCCGGGC[A/G]TGGTGGCGTGTGCCT | 54793 |
rs138903824 | in-del | -/CT | 0.186421 | 0.24178 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454434 | GAAGTAAAAAAAGCA[-/CT]CTGTGTTCAAGACGT | 54793 |
rs138937232 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443113 | TCCTATAACATACAT[C/T]ATATACAAATTTTAT | 54793 |
rs138938323 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456058 | TTCATTCAATACACA[A/G]ACAATTCCTGGCGAG | 54793 |
rs139000837 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449476 | CTTAATACTTAATGT[A/C]ATATTATAGCTTAAG | 54793 |
rs139063721 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444017 | AAAACAATTGTTTCT[A/G]AGATCAAAACTACCT | 54793 |
rs139075991 | in-del | -/ACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430809 | TCCAACATAATAAAT[-/ACAC]ACACACACACACACA | 54793 |
rs139271719 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434550 | TTTTCCTGTTTTGCT[A/G]CTAACCTGACCCTTC | 54793 |
rs139348204 | snp | A/G | 0.000313105 | 0.0125082 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429866 | AAATTCTCATCTGAC[A/G]CTTTGTGACATGTGT | 54793 |
rs139413085 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431913 | AAATTTAAAAATCAA[-/T]TTCTCATTTGCACTA | 54793 |
rs139415573 | snp | C/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25433340 | CTCACCTTCTAAATT[C/G]GCTTTAAGACCAGAA | 54793 |
rs139618175 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457188 | TGAATAATCGGAAAG[C/G]CATTTTTAATGCCAC | 54793 |
rs139839544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438736 | ACAAAAATCTTGTGA[G/T]GTAGATAGGGTCAAG | 54793 |
rs139846974 | snp | A/G | 0.000148355 | 0.00861134 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429920 | TATAGCTCCCTTCAC[A/G]TTGGACCCTCTCAGG | 54793 |
rs139935197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427750 | ACAAACAAATTAAAC[A/G]AATTATTGGGGAGGC | 54793 |
rs140049773 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431846 | TTATACCAGATTTCA[C/T]AGCTACCAGCCACAT | 54793 |
rs140107334 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448116 | CTGGACATGATGGGA[C/T]GGAAAAGAAAAAAGG | 54793 |
rs140144689 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451285 | AAGATGATTAAGTTA[C/T]GGAGAAAGTTGCAAA | 54793 |
rs140177249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446505 | GGTGTGTTAAATAGC[A/G]CTCCAGTTGTGAAGT | 54793 |
rs140289275 | in-del | -/GAGAA | 0.147656 | 0.228091 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448199 | AAAGGAAAGCAAAGC[-/GAGAA]GAGAAGAGACATGAA | 54793 |
rs140752715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441477 | ATAGATCAAAATTAT[A/G]ATCTAATATTCCAAA | 54793 |
rs140774286 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453272 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 54793 |
rs140805443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440024 | GTTAATTTTTACTTA[C/T]ATTGTGTGTTTATTA | 54793 |
rs140818604 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437126 | ATTGTAAAACAAACG[A/T]CATCCAAGGTACAGC | 54793 |
rs140869631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434962 | CATGTTTATTTCAAA[A/G]TATCTGTCAAATACT | 54793 |
rs141194444 | in-del | -/ACACACACACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430809 | TCCAACATAATAAAT[-/ACACACACACAC]ACACACACACACACA | 54793 |
rs141240299 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459306 | TTCGAACCCGGAGCC[A/G]GAGGTCCCGACGGCT | 54793 |
rs141351948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454022 | AAACCTGGATACTTA[C/T]TACTAACAACATATT | 54793 |
rs141413841 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448816 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATTGC | 54793 |
rs141428355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449839 | AAAAAAAATGAAGAA[A/G]AAAAAACACAACTAT | 54793 |
rs141703578 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437333 | ATGCAGCCAGGATAC[A/G]TTTCCAATTCTAGGT | 54793 |
rs141745884 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442740 | TATATGTTCCGACAA[C/T]TCAGAAACAATACAA | 54793 |
rs141771411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433784 | CTATGCATGACAATG[A/G]AACAGTCAAAATGTA | 54793 |
rs141809412 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434250 | AATTACAGGCATGCA[A/C]CACCACGCCTGGCTA | 54793 |
rs141835705 | snp | A/G | 3.29804e-05 | 0.00406068 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446210 | AGTTTACTGCTGGCC[A/G]CAGAAAGCAAATCAG | 54793 |
rs142080208 | snp | C/G | 0.000905596 | 0.0212598 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460397 | AGGAAATGCCTCTTT[C/G]ATTTTGGGAACTGGG | 54793 |
rs142144689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456167 | CTACTAAACAAGCTA[C/T]GAGAGGGAAACTTAC | 54793 |
rs142437692 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432906 | AAGGGAGTGAAGTAG[C/T]CTCCTAAATATACAA | 54793 |
rs142496121 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427539 | TCCTGTCATCCCAAC[A/C]GCTGTATTTTTACCT | 54793 |
rs142552124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430156 | TATCTTTATTTGTTA[C/T]CTCTAGTTCAGGCTG | 54793 |
rs142563986 | snp | C/T | 1.65102e-05 | 0.00287312 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435440 | CAAGATTACAGCGGC[C/T]TAAATTGGCCATTTT | 54793 |
rs142925982 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445071 | GATGAGGATCATCAT[A/C]CAACAATGTGACTCA | 54793 |
rs142933546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443258 | AAAAAATCAAGGCTT[G/T]TTGGAAAAATGTTGA | 54793 |
rs143125167 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448686 | ATGGGAGGCTGAGGC[A/C/G]GATGGATTGCTTAAG | 54793 |
rs143468225 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427814 | GTGTTGTTAGCATGG[G/T]GTATTTTTAAAAGAA | 54793 |
rs143515891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442430 | AGGATTTTTCAATAG[C/T]TTCACTGAGGTATAA | 54793 |
rs143658803 | snp | C/G | 0.000197775 | 0.00994225 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440658 | CCCTCAGGAGGCTTA[C/G]AATCTGTCTGAGGAT | 54793 |
rs143836319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439508 | TTTTTACTCTTAAAA[A/G]CTGACATAATTAGTA | 54793 |
rs143865236 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451350 | TTTTGAGAAAGAGGA[C/G]CAATAAAAATCTTGT | 54793 |
rs143869476 | in-del | -/A | 0.0205511 | 0.0992634 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430249 | TATAAGGAGACATTG[-/A]AAAACAGGGGTCCCC | 54793 |
rs143949976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446838 | CCTCATTTATTTAAT[C/T]CTTCACTAACTAAGC | 54793 |
rs144035295 | in-del | -/TA | 0.120326 | 0.21374 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446875 | TAGCATCTAACATTT[-/TA]AAGAACAGAGCAAAC | 54793 |
rs144158585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438289 | ATAGAACTAGCTAAA[A/G]GGGTCAAATAATATC | 54793 |
rs144269062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456884 | GAAGTTTGTTTTTGA[A/G]AAATATTACCAATTT | 54793 |
rs144577310 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433882 | TAAGTGAAATTCTTG[A/T]TATTCTAAGATGCTA | 54793 |
rs144610167 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441661 | ACACAATAGACAATG[A/C]CTTAAGGGAAAGAAA | 54793 |
rs144647436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437273 | GGTTCTTGTGGGCCA[C/T]GCTCTCAATTTGCCA | 54793 |
rs144742655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444543 | AATAAGATCTTGCAC[A/G]TGAAAGTACTTTTGA | 54793 |
rs144829990 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435244 | CAACATAATAAATTA[C/T]CTGTTTTCAAGTAAA | 54793 |
rs144948302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448506 | GTCAATGAATTACAC[A/G]TTTAAAAAATGGTTA | 54793 |
rs145029103 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459473 | AGGTGCGGCGTGAGA[G/T]GTAGGATTGCATCCG | 54793 |
rs145073209 | snp | A/T | 0.107694 | 0.205546 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455230 | ACTCCGTCTCAAAAA[A/T]TAATAATAATAAATA | 54793 |
rs145181952 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458961 | GGAGTTAAAGCGCTA[A/G]GAGAAGCGTTACTCC | 54793 |
rs145248197 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457332 | CTGAGTTACTTCTAG[A/G]TATCATTTAGCAACG | 54793 |
rs145412341 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434783 | GAACTTAAAGTTGTT[A/G]AAAATTAATAGATTT | 54793 |
rs145420181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441115 | CTTCCATGGACAAAG[C/T]CCCATACTGATAAGA | 54793 |
rs145477833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430079 | AAAATGTTCTTATAC[A/G]ATAAAACTCAGTTAA | 54793 |
rs145506895 | in-del | -/TATTAAAATTAAAAGT | 0.105924 | 0.204309 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449672 | ATTTAAATTTTAATC[-/TATTAAAATTAAAAGT]TAAAATGCAGTTCAG | 54793 |
rs145610219 | snp | A/G | 0.000198014 | 0.00994827 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458248 | GTCACCCGCCTCATC[A/G]CGCTGCCCCCGCTGG | 54793 |
rs145833720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435255 | ATTATCTGTTTTCAA[A/G]TAAAAGCTCCAGTAA | 54793 |
rs145978416 | snp | C/G | 0.00120227 | 0.0244885 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429892 | TGTGTAGTGGTGTCA[C/G]CATCTCTTCAAATAT | 54793 |
rs145980364 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432996 | AAATGATTTTTAAAA[A/T]CTCCCTGGCTTTATG | 54793 |
rs145990893 | snp | C/T | 0.00305925 | 0.0389906 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460450 | ATGCCGAATTACCTC[C/T]TAATCCTTGCACACC | 54793 |
rs146122622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450956 | TCAGGCAGTTAACAA[C/T]TTCCTTTAAGTGAAA | 54793 |
rs146141380 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445338 | GTCTAGAACTGATTA[A/C]CTGCAAAGCAGTATA | 54793 |
rs146151321 | in-del | -/GTTTTTTTGATGTTA | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434516 | TTAGGTCCTTCAAAC[-/GTTTTTTTGATGTTA]GTCTTTTTCCTGTTT | 54793 |
rs146278610 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428784 | TGTAATCAAATGTGT[A/G]TTTAAAATTCCTCAT | 54793 |
rs146381698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456212 | ATTATTCTTATAACC[A/G]GGAAACAAAAGCAGA | 54793 |
rs146399536 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452039 | ACAAGTATTTATTGT[A/G]CATTATGTAATATAC | 54793 |
rs146659100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447946 | TGCCTGGCCAACATG[A/G]TGAAACATGGTCTCT | 54793 |
rs146677574 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441873 | CGGGCATGGTAGCAC[A/C]CATCTGCAGTCCCAG | 54793 |
rs146728920 | snp | A/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436246 | TTACCTGGCATCGCA[A/G]TTCTGACTTGGTTGG | 54793 |
rs146808650 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454652 | TTTAAAAAACAAAAA[A/C]AAAAAAAACCCTCAA | 54793 |
rs146928495 | in-del | -/TTG | 0.0337553 | 0.125452 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454051 | TTTCTTTTTCATTCT[-/TTG]TTGTTGTTGTTGTTT | 54793 |
rs147003189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454039 | ACTAACAACATATTT[C/G]TTTTTCATTCTTTGT | 54793 |
rs147018492 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449446 | TGCAAGTTGAATGCA[C/T]CTGCCTGTATTATGC | 54793 |
rs147243866 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443621 | GACAGACAGACAAGA[C/G]TATGCACTTACTTCT | 54793 |
rs147260647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439956 | GATCTTCCAAACTTA[C/T]ATTTTTCTGCCCTTT | 54793 |
rs147642906 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454255 | CAAGAATGAAAACAC[A/C/G]GTACAGAATGAAAGT | 54793 |
rs147699053 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434856 | GATAACTGTTATAAA[C/T]ACATACATATACATA | 54793 |
rs147715377 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430142 | TTAAGATGTTCTTCT[A/G]TCTTTATTTGTTACC | 54793 |
rs147743765 | snp | C/G | 1.65149e-05 | 0.00287353 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435433 | GCATGTGCAAGATTA[C/G]AGCGGCTTAAATTGG | 54793 |
rs147804247 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457137 | GCCAACAAACCACAC[C/T]CTGGTTCGAATTTTC | 54793 |
rs147819495 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453718 | CTATTTAAAAACACA[C/T]GGCAAAGAGAAAAAC | 54793 |
rs147908032 | snp | A/G | 3.36264e-05 | 0.00410026 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439292 | ACCCAATAAATTAAT[A/G]CCATCATTTACAATG | 54793 |
rs148020135 | in-del | -/CAAA | 0.0232847 | 0.105357 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451297 | TTACGGAGAAAGTTG[-/CAAA]CAGACTGGCACATGC | 54793 |
rs148024976 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442734 | AATGGCTATATGTTC[C/T]GACAATTCAGAAACA | 54793 |
rs148376955 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431021 | TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG | 54793 |
rs148390469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452678 | GCTGCTGTGTGCCAG[G/T]ATACATATACAGAAA | 54793 |
rs148468700 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454435 | AAGTAAAAAAAGCAC[A/T]CTGTGTTCAAGACGT | 54793 |
rs148620296 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456579 | TGTAACATAAACATA[C/T]TTATATTTAATTATT | 54793 |
rs148948509 | snp | C/G | 0.000183543 | 0.00957798 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439384 | AGAAAGCTCCTCTAT[C/G]ATCTTGCTTATTTCC | 54793 |
rs148952788 | snp | A/G | 0.000858596 | 0.0207017 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429971 | CCCAGACAGATCACA[A/G]TTCTGCAAGATGAAA | 54793 |
rs149005548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435766 | TTTCTGTGTAGAAGC[G/T]TCTAAAGAGGGATCC | 54793 |
rs149276498 | in-del | -/AAG | 0.021333 | 0.101051 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446452 | CCTCAACTAGAACAT[-/AAG]AAATCATCTCTGACC | 54793 |
rs149604359 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440493 | CATTTGAGTATCTTT[-/T]AAGGAAATCAGCAAA | 54793 |
rs149652007 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456531 | TGGCTTTGCTTCTTT[C/T]TATCTAGTACTCTCC | 54793 |
rs149773075 | snp | C/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429057 | TGTAAATAGATAGAA[C/T]TGCTTGATCTGGTGT | 54793 |
rs149784610 | in-del | -/TTTAC | 0.26818 | 0.249338 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427861 | GTTTAAAGAAATAAA[-/TTTAC]TTTAATGGTACTTTC | 54793 |
rs149897434 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448455 | TACTGGAAATAAACC[A/G]TGGTGATGGTTACAC | 54793 |
rs150053242 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441088 | CTCTTAAAACCAAAT[A/G]GCCAAAACTCCCTTC | 54793 |
rs150071535 | snp | C/T | 1.68806e-05 | 0.00290517 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25433376 | CTCAAAATTACACAG[C/T]TTCAGGGATGCTCCT | 54793 |
rs150154361 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442956 | TCAGGACTATTGATA[C/T]AGAAAAAGGAGACAC | 54793 |
rs150174762 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25458540 | TCACCGGACAGAGTC[C/T]AGCCAATCAGCACCC | 54793 |
rs150839497 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449850 | AGAAAAAAAAACACA[A/G]CTATTTTAATTCTAT | 54793 |
rs150941329 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453125 | CCCAGTACTTTGGGC[A/G]GCTGAGGCGGGCAGA | 54793 |
rs150994663 | snp | A/G | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457614 | TTTGGCGGCGGCGGG[A/G]CGTGGGGGCTTGAGG | 54793 |
rs151294023 | snp | A/G | 0.000164799 | 0.00907592 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440559 | TTCTCTTTCTAACAC[A/G]CATACACACACACCT | 54793 |
rs180779455 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447614 | TACGAGTGTGCAGTT[A/T]TTCAAAAGCAGAGTA | 54793 |
rs180837403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460039 | TACGAATTGCATGCC[C/T]GTATCAAAATATTTC | 54793 |
rs180872832 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454321 | CACATACTCAGAAGG[C/G]ATTTACTAAGTGTTC | 54793 |
rs180900778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434630 | GTAGATTTTGTTACT[C/T]GCCCTGATACACAGC | 54793 |
rs180920275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443614 | AGGTAGAGACAGACA[A/G]ACAAGAGTATGCACT | 54793 |
rs181362058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443231 | TTTGTCTTGGAATGA[C/T]ACTTCCCACTAAAAA | 54793 |
rs181526503 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442811 | AACATTTAACTGTTT[G/T]TAGTAATTATATTGG | 54793 |
rs181546757 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435744 | AATATAGCCCGGCTA[A/T]AATTCATTTCTGTGT | 54793 |
rs181550699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454690 | ACCAAAGATTCCAGT[G/T]ATTAGAACTAAGGCC | 54793 |
rs181578222 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429541 | TATTTCCACATCATG[C/T]CTATTTAAAAGCAAA | 54793 |
rs181937314 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439052 | CTTACATATTTAGCT[A/G]TATGTACAAAGACTA | 54793 |
rs182082318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438948 | GTTACATTCTTAATT[A/C]AATTTTTAAAAAAGG | 54793 |
rs182089344 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458801 | AGCCCCTCCTCCAGC[A/G]TTAGCCCCGCCCACA | 54793 |
rs182278817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436595 | TAACATTTAATTGCC[G/T]TTTTAAATGGAGCAG | 54793 |
rs182495101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451018 | AATTAAAATTAATAC[A/G]AAGAATCTTATAGTT | 54793 |
rs182531239 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445500 | CAAAGCAATGATAAC[A/G]TAAGTGGCATAGTCA | 54793 |
rs182561100 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448266 | TTTGACAGTATGCTA[A/C]ATGAAATAAGCCAGT | 54793 |
rs182748393 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431813 | TAAATTTTGACATAC[C/T]GTTCTCTGCTATCCA | 54793 |
rs182819331 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437254 | CTCAACATATTATAA[A/G]AGAGGTTCTTGTGGG | 54793 |
rs182872881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456758 | TTAATTTTTGACAAC[A/C]AAATTGAGTGGATTT | 54793 |
rs183105213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431219 | GGGAAGACTTTTTTT[A/T]TAATCTGAAAAGATT | 54793 |
rs183113828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450431 | ATGTTGAGTGTTGAA[A/G]TAGGACACACCTTTT | 54793 |
rs183177894 | snp | A/G | 0.00198222 | 0.0314195 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436207 | GATTTGCTGATAGAA[A/G]TAATTGATGTAAAAG | 54793 |
rs183336125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444085 | GCATTTTAACGGCAT[A/G]TAAAACATGCATCTA | 54793 |
rs183437824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454929 | AATACAGGATTGACT[C/T]TAAACATTAAAATAA | 54793 |
rs183676649 | snp | C/T | 4.95127e-05 | 0.00497533 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432558 | ACAGTTCTTCAACTT[C/T]GCATTTTTTAAGGTA | 54793 |
rs183730326 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441107 | AAAACTCCCTTCCAT[A/G]GACAAAGCCCCATAC | 54793 |
rs183768616 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441582 | CAAGAACTCCCAAGA[A/G]AATTAGAAATAAAAG | 54793 |
rs183817821 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429749 | AAATGTTTTTTTTTT[A/G]AATTTCCTTACAGTG | 54793 |
rs183859599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452476 | TCAAATGTGTGATCC[C/T]GTCACCTGCAGCATC | 54793 |
rs183873681 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447066 | TTGTGCAGTTGCACC[A/G]TTATCAGTTATGACC | 54793 |
rs183919200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438555 | ACTTTGCACATGGCA[A/G]TGATCTGCTGAAGCT | 54793 |
rs183924125 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457558 | TACCCGTCCTCTAGG[A/G]AATCAAAATAAGGCA | 54793 |
rs184312561 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453612 | GAGCCAGAGATCATG[C/T]CACTGCACTCCAACC | 54793 |
rs184400053 | snp | A/G | 1.71437e-05 | 0.00292772 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433304 | TGCTTCCTTCGTAGA[A/G]TAGGTATTTACAGAA | 54793 |
rs184410037 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427982 | GAAATGTAAGCAAAA[G/T]ACAGAAAGTGATGAT | 54793 |
rs184423951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434056 | ATGCATAATGCAGGG[C/T]AGAGAGTAAAATGGT | 54793 |
rs184453121 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453160 | GAGGTCAGCCGAGAC[C/T]AGCCTGACCAACATG | 54793 |
rs184501056 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439000 | TCACTTGTGATAGAA[C/T]GTAAATCAATTTAGA | 54793 |
rs184508090 | snp | A/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458803 | CCCCTCCTCCAGCGT[A/T]AGCCCCGCCCACAAG | 54793 |
rs184544240 | snp | A/G | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446182 | ATTATACACACTGGT[A/G]GCTTTTATGCCGAGT | 54793 |
rs184554212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438329 | TTTTTTTGCAATAGG[C/T]ACATGTTCAAGGGAA | 54793 |
rs184696853 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456962 | CAGGTAGTAGCTAAG[C/T]ACAGAACAGGTTTAG | 54793 |
rs184735586 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441882 | TAGCACACATCTGCA[C/G]TCCCAGCTCCTGGTT | 54793 |
rs185170991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446544 | CCTACACTTCGATCT[A/G]GAGTCTGACATTTTC | 54793 |
rs185193923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440391 | ACTGAAGTGATGCCT[A/T]TTATGCTTTCTCTGG | 54793 |
rs185273429 | snp | C/T | 0.0182019 | 0.0936463 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428920 | TATCTATTTCTAAGC[C/T]GGCCCTATGTAAACT | 54793 |
rs185434422 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442841 | GTACTGAAAGTATTG[A/C]GTTTGTTACTCTGAC | 54793 |
rs185493143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443333 | TTCCAGATAATAAGA[A/G]AGCCATAAAATCCAA | 54793 |
rs185568789 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431253 | CTTAATCAAATTGTG[G/T]AATAGATTTTTCCAT | 54793 |
rs185574972 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450638 | GGCCAACATGGTAAA[A/T]CCGTGCCACCACGCC | 54793 |
rs186100331 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430194 | TAAATATGTATAAAC[A/T]AAGGTTAAAGAGGAA | 54793 |
rs186193954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447927 | AGCCCAGGAGTTCGA[A/G]ACCTGCCTGGCCAAC | 54793 |
rs186199501 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435997 | AAACTGCTGCAATTT[A/C]TATGCATTATTCATA | 54793 |
rs186210832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454777 | AACATCTGTATATTT[A/G]TGTATTTATGAACTA | 54793 |
rs186247422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439116 | CTATTTCTACACCTA[C/T]ATCACTCATATACAT | 54793 |
rs186342998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435149 | TTATTAGTTACTAAA[C/T]CTTTCAAGTCTATGT | 54793 |
rs186348067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455182 | GTGAGCTGAGATCAC[A/G]CCACTTCACTCCAGC | 54793 |
rs186350413 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454461 | GACGTATAGAAACTC[C/T]GCACTGACATTAAGT | 54793 |
rs186357085 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459019 | GAGGTCACAAGGCAG[A/T]GGCAGGTGTCTGTAG | 54793 |
rs186602295 | snp | A/T | 1.64882e-05 | 0.00287121 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436351 | AAAAGACATTAAGAA[A/T]TTAGTGGAGTCTTTT | 54793 |
rs186949056 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441627 | AAGACTAAAGCAAAA[G/T]AAATACAAGAGTGAT | 54793 |
rs187042092 | snp | C/T | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443921 | CAAACACTACTTACG[C/T]AAGCAATATTTACTC | 54793 |
rs187182805 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427764 | CGAATTATTGGGGAG[A/G]CAGTCTTTTCTTTTG | 54793 |
rs187189017 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445971 | CTGATCAATTCACCT[C/T]AAGCCCAAATGATTT | 54793 |
rs187216221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448344 | ACACAGGCAAATTCA[C/T]AGAGAAAGAAAGCAG | 54793 |
rs187510291 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456819 | CTAGGTTTAAATATT[A/C/T]GTCTTCCATGAGTAA | 54793 |
rs187697931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455669 | TTTGGTGAGGGTTAA[G/T]TTGGTTAAAACTAGA | 54793 |
rs187771669 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432065 | ACAGCTATCAAGTCT[C/G]CTAGCTAAACTGGCA | 54793 |
rs187832491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452543 | TCCTACCCCACCCCA[C/G]ACCTACTGAATATTA | 54793 |
rs187913356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441158 | AATCCAAGTTGAATG[A/C]AACAAAGACAACAGA | 54793 |
rs188062057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451120 | TTGTTTTCCAACTAA[C/T]CATTCGCACATACTA | 54793 |
rs188069652 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457170 | AGCATGTTTACTCTA[C/T]ACTGAATAATCGGAA | 54793 |
rs188456459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453422 | GCACTTTGGGAGGCT[A/G]AGGCTGGCGGATCAC | 54793 |
rs188494227 | snp | A/C | 2.15288e-05 | 0.00328084 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433451 | CTGCAAAGAAAAGAG[A/C]AAAGTCCTGGTTGTA | 54793 |
rs188528592 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437571 | TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCAGG | 54793 |
rs188599457 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447377 | TTATGACCAAGCAAG[A/G]CTCTGTCTCCCCGCT | 54793 |
rs188637851 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429775 | CAGTGTTATTTCTTC[C/T]AGACAACTGAGTGGG | 54793 |
rs188722125 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446360 | TATCATATAAAAGGA[A/G]ACTTCAAAAGGTTCT | 54793 |
rs188769557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446789 | TTATTATATCATTAA[C/T]GACATCAACTACCAC | 54793 |
rs188843820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445002 | GGACATCACAGGACA[C/T]GTTAAATTTTTCTAA | 54793 |
rs188989934 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428201 | TGAAAATATAGTACA[C/G]AGTGAAATGATTTAA | 54793 |
rs189004431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434095 | TATGTTTTAAGACTT[C/T]ATTTTTTTGTTTTGT | 54793 |
rs189059794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440712 | ATACAAATATTAAGA[C/T]TGGGGATTCTGGGAA | 54793 |
rs189101436 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429210 | GATGTCTTTCTTTCC[A/G]CTCTGTCTCAATCAG | 54793 |
rs189296097 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453886 | TATGTATCAAATATA[A/T]TAAGAAATGTTCAAG | 54793 |
rs189380778 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438583 | GCTGACAGGCATGTG[A/G]CCTCAAGATTGCCAA | 54793 |
rs189388801 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458704 | GCAGGCGCACCCTCT[A/G]GTTTAGGTAGCGCTT | 54793 |
rs189493614 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443023 | AATCCTTAATATAAA[C/T]TTTAAGTACTACTAT | 54793 |
rs189522332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435738 | CATTAGAATATAGCC[C/T]GGCTATAATTCATTT | 54793 |
rs189523322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443534 | CCAATTAAGTGACCA[C/T]TGCCTGCCAGTCACT | 54793 |
rs189532161 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454586 | AAATGTTGAGGCACA[C/T]GGAAAAAGGATGACA | 54793 |
rs189833058 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439040 | TGATGCGTATGGCTT[A/C]CATATTTAGCTATAT | 54793 |
rs189928444 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438399 | TTTTGTATTTCACTA[C/T]AGAAACTGTAAGCCA | 54793 |
rs190093234 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458906 | ATTGGTTGAATGAGT[C/G]TTTTCGAAGTTTGCA | 54793 |
rs190209260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445475 | TGCCAATTAAATGGT[A/G]TAACTCAGGCAAAGC | 54793 |
rs190243160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454815 | CTGTTAGAAAGTACA[C/T]GTTTTCCCAAATGAT | 54793 |
rs190371090 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448109 | CTCCAGCCTGGACAT[G/T]ATGGGACGGAAAAGA | 54793 |
rs190388232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451017 | GAATTAAAATTAATA[C/T]GAAGAATCTTATAGT | 54793 |
rs190450898 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431085 | ATTCGCCCACCTTGG[C/T]CTCCCAAAATGCTGG | 54793 |
rs190458860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449011 | GAGGTATTCTGTAAT[C/T]GCATTATACACATTC | 54793 |
rs190601237 | snp | A/G | 1.78376e-05 | 0.00298638 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436497 | ACACCTATCAGAACA[A/G]AAATAATTCTGAAAC | 54793 |
rs190612474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430283 | CCCTGGGCCACAGAC[C/T]GATACTGGTCCATGG | 54793 |
rs190728202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442735 | ATGGCTATATGTTCC[A/G]ACAATTCAGAAACAA | 54793 |
rs190843849 | snp | A/G/T | 0.00373485 | 0.04307 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440567 | CTAACACACATACAC[A/G/T]CACACCTACCGTGTA | 54793 |
rs191310765 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427896 | AAAAAGACTAATCCA[C/T]AACAAATTAAGTTAT | 54793 |
rs191313503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459648 | TAGAGCTGCGTCTTG[A/G]GAGGGGTACCCTTAT | 54793 |
rs191319426 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431559 | TGATCAGTCTTTGCA[A/G]TCAGAGAGAGGGAGG | 54793 |
rs191322897 | snp | A/G | 1.65296e-05 | 0.00287481 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25446136 | AAGGTTACCTGATCA[A/G]AGCAATATCATCAAT | 54793 |
rs191411266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436072 | TTGCATCTCTTTTTC[A/G]TTAACCATTTCAGAA | 54793 |
rs191462475 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440931 | AGCAACAGGGTATAT[A/G]ATGAACCCATGAATG | 54793 |
rs191467295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441828 | AAAACCCCAAAACCC[C/T]ATCTCTACAAAAAAT | 54793 |
rs191492119 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439261 | ACATAATTATATTGA[A/G]AGTCTAAATAAACTC | 54793 |
rs191869920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441504 | CAAAACATGCTAAAA[G/T]AAGTTTATACAAGGT | 54793 |
rs191935381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452667 | GAAAAATGCTTGCTG[C/T]TGTGTGCCAGGATAC | 54793 |
rs191979092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433237 | CTATCCCCTACAGCT[A/G]TCCTGTTTCACCCTT | 54793 |
rs192097022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446820 | AGAAAAGATAACTTC[C/T]CACCTCATTTATTTA | 54793 |
rs192187591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438494 | TAAAATTTTAGATAC[C/T]CAGGTTTTCTTTAAA | 54793 |
rs192436821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444073 | TATACCTCCAGAGCA[G/T]TTTAACGGCATGTAA | 54793 |
rs192593749 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457200 | AAGCCATTTTTAATG[C/T]CACTGGACAATTTCA | 54793 |
rs192612553 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455925 | AGGTATATTTCTTCC[A/C/T]GACCTCCAATAAATC | 54793 |
rs192651644 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437212 | AAGATTATGCCATTC[C/T]GTTCGGATATATATC | 54793 |
rs192792573 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433702 | TTACATGAAACATAA[C/T]GGTTTAGATAAAGAA | 54793 |
rs193004020 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453479 | GCCAATATGGTGAAA[A/C]CCTGTCTCTACTAAA | 54793 |
rs193089136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451366 | CAATAAAAATCTTGT[A/G]TATCATGGACATAAG | 54793 |
rs193129108 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428254 | TTATGAAAATAGATT[A/C]TCTCTCAATACAATA | 54793 |
rs193162208 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437627 | ACCTTACAGTGAGCC[A/G]AGATCGCGCCACTGC | 54793 |
rs193245378 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432070 | TATCAAGTCTGCTAG[C/T]TAAACTGGCAAATTA | 54793 |
rs193283911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446441 | TATTGCCGACTCCTC[A/G]ACTAGAACATAAGAA | 54793 |
rs199536181 | snp | A/G/T | 8.85873e-05 | 0.00665476 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439259 | TTACATAATTATATT[A/G/T]AAAGTCTAAATAAAC | 54793 |
rs199554076 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441177 | AAAGACAACAGAGAC[A/G]AAAAAAAAAAAGGAC | 54793 |
rs199637142 | in-del | -/TATACTG | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427909 | CATAACAAATTAAGT[-/TATACTG]TATTTCCTTTGCTAC | 54793 |
rs199691398 | in-del | -/TTAAA | 0.00636936 | 0.0560724 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435827 | TAAACCTAATTATAT[-/TTAAA]TTATTTTATTAATTC | 54793 |
rs199860581 | snp | C/T | 0.000857718 | 0.0206911 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436401 | TGTAACACTGGCTAA[C/T]GTAAAAACAGGCTTA | 54793 |
rs199882011 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459782 | TTAAAAGTACGCGCT[-/TA]GAGTAAAAGAATGGT | 54793 |
rs199896035 | snp | C/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429954 | GCTTCTTGAAGATCA[C/T]ACCCAGACAGATCAC | 54793 |
rs199928317 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450764 | CCCAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 54793 |
rs200090996 | snp | A/G | 0.000181418 | 0.0095224 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460207 | TCATCTTGCTGGTGG[A/G]GTTATTTTTCATTGT | 54793 |
rs200214302 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437796 | TAGGTTGCAGTGAGC[A/C]GAGATCACACCATTG | 54793 |
rs200413669 | snp | A/C/T | 1.65143e-05 | 0.00287348 | synonymous-codon, missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432567 | CAACTTTGCATTTTT[A/C/T]AAGGTAGCCACTCTC | 54793 |
rs200463615 | in-del | -/ACACAC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430809 | TCCAACATAATAAAT[-/ACACAC]ACACACACACACACA | 54793 |
rs200467071 | snp | C/T | 0.000593061 | 0.0172098 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440570 | ACACACATACACACA[C/T]ACCTACCGTGTAGTT | 54793 |
rs200476271 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427865 | AAAGAAATAAATTTA[G/T]TTTAATGGTACTTTC | 54793 |
rs200541990 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429739 | ATAATCCTCTAAATG[-/T]TTTTTTTTTAAATTT | 54793 |
rs200603217 | snp | C/T | 1.64974e-05 | 0.00287201 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429845 | TACATCTTCCTCCAG[C/T]CCCTAAAATTCTCAT | 54793 |
rs200603242 | in-del | -/C | 0.0193772 | 0.0965046 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453159 | GGAGGTCAGCCGAGA[-/C]CAGCCTGACCAACAT | 54793 |
rs200643642 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449836 | AAAAAAAAAAATGAA[A/G]AAAAAAAAACACAAC | 54793 |
rs200690326 | snp | A/C | 0.00192842 | 0.0309918 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432476 | AAGTCTAGAGTAATA[A/C]AAATTCTTAAAGTGT | 54793 |
rs200827135 | snp | A/C | 0.00019977 | 0.00999226 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440683 | GAGGATCTAGAGATG[A/C]CATGTAGAAAATAAT | 54793 |
rs200868916 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435916 | GAAATGCTATAGTAC[A/C]CATAAGTAAAGTACC | 54793 |
rs200903987 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460417 | TGGGAACTGGGAAGA[C/T]TGTGACTCCTCAGAA | 54793 |
rs200962577 | snp | C/T | 4.94434e-05 | 0.00497184 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436290 | AATCGGACAAATTCC[C/T]TTCGGGATATTGGTG | 54793 |
rs201029805 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433278 | TTCCAGGGCTTTTTT[-/C]CTTTACAGTCTGCTT | 54793 |
rs201030198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432465 | AGATGCTTAGTAAGT[A/C]TAGAGTAATAAAAAT | 54793 |
rs201205368 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452224 | GATAATTTAAAAAAA[-/A]GATGAGATAATTAAC | 54793 |
rs201250701 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430471 | GTGAACTGCACATGT[A/G]AGGGATCTAGGTGGG | 54793 |
rs201295223 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446872 | TTTTAGCATCTAACA[-/T]TTTAAGAACAGAGCA | 54793 |
rs201361170 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438305 | GGGTCAAATAATATC[-/T]TTTTTTTTTTTTTTT | 54793 |
rs201362150 | snp | A/T | 0.00299557 | 0.0385851 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25432531 | TCCTGCCAGAGTTGC[A/T]CCTCTGAGGTTACAG | 54793 |
rs201368879 | snp | A/G | 0.000208427 | 0.0102064 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435552 | CACCATAACTAAATC[A/G]TCTGTTTGTATTAAA | 54793 |
rs201590210 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448919 | CAAGAAAAAAAAAAA[-/A]GAAAAAAAAGCCTGA | 54793 |
rs201653606 | snp | C/T | 9.88338e-05 | 0.00702902 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460264 | AATTCAAAAGACAAG[C/T]CCCCTGAAACCAAGG | 54793 |
rs201732101 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450751 | ACCGCCTCAGCCTCC[A/C]AAGTGCTGGGATTAC | 54793 |
rs201752732 | snp | C/T | 1.64803e-05 | 0.00287052 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439571 | CAGATATAAAACAGG[C/T]AAGATGAAATGTGAA | 54793 |
rs201784454 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450233 | TCCTAAAGGTCCAAT[-/A]AAAAAAATTAATTTG | 54793 |
rs201992906 | snp | A/G | 0.00299541 | 0.0385841 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429804 | GGTGGAGAAAGAAAA[A/G]TGATAAGGAAAACAT | 54793 |
rs202000203 | snp | A/G | 0.000115307 | 0.00759211 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460246 | ACCTCTTAGATGGAT[A/G]CCAATTCAAAAGACA | 54793 |
rs202013970 | snp | C/T | 0.00207535 | 0.0321461 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25433430 | GACTCCCTGGAGATT[C/T]GCACACTGCAAAGAA | 54793 |
rs202069117 | snp | C/T | 3.30967e-05 | 0.00406783 | intron-variant | KCTD9 | GRCh38.p7 | 8:25429991 | GCAAGATGAAAACAA[C/T]ATTCATGTAATTCAT | 54793 |
rs202201329 | in-del | -/G | 0.0151446 | 0.0856909 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452915 | CTCATGCCTGTAGTC[-/G]CAGCACCTTGGGAGA | 54793 |
rs367627932 | snp | C/T | 3.29468e-05 | 0.00405861 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460353 | TAGACAGAGAGTTGT[C/T]CTCACCCCTACAATA | 54793 |
rs368089197 | snp | C/T | 1.64776e-05 | 0.00287028 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439592 | GAAATGTGAAAACAA[C/T]GTGTTACACTCACCT | 54793 |
rs368209221 | snp | C/T | 0.000234157 | 0.0108177 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432661 | AACACATTCTGGGAG[C/T]AGTTTAACTTAAAAA | 54793 |
rs368212807 | snp | A/G | 1.65501e-05 | 0.00287659 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439711 | CATTTGTCTTTATAA[A/G]CAAACATATTTAAGT | 54793 |
rs368385732 | snp | A/G | 1.66543e-05 | 0.00288563 | stop-gained, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439360 | AGTACTCAGGACTTC[A/G]GTCAATTAAGAAAGC | 54793 |
rs368464192 | snp | C/T | 1.6473e-05 | 0.00286988 | utr-variant-5-prime, missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460265 | ATTCAAAAGACAAGC[C/T]CCCTGAAACCAAGGA | 54793 |
rs368464821 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449698 | AAAGTTAAAATGCAG[C/T]TCAGTCACACTAGCC | 54793 |
rs368639879 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445374 | CTGAAAGGTCATTTT[G/T]ATCTAGATTTATACA | 54793 |
rs368718646 | in-del | -/GAA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446454 | TCAACTAGAACATAA[-/GAA]ATCATCTCTGACCAA | 54793 |
rs368832899 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433947 | GCCAGCATTTAAAGG[C/G]ATTATTTAGCTAGAA | 54793 |
rs368882687 | snp | A/G | 0.000157988 | 0.00888645 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458194 | CCCCCTCACGCCCCC[A/G]TTACCTTTCCGTTCT | 54793 |
rs368893617 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440207 | GGGACTACAGGCGCC[C/T]GCCACTACGCCCGGC | 54793 |
rs369043890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445298 | GCTTCACAGGTAATT[C/T]GTTTCCTCATCTGTA | 54793 |
rs369052120 | snp | A/G | 3.29777e-05 | 0.00406051 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439677 | CTCCTAAGAATTCAG[A/G]GAAAAAAATTGATTT | 54793 |
rs369086712 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460064 | TATTTCATGTACCCC[A/G]TAAATTATACATCTA | 54793 |
rs369161280 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433703 | TACATGAAACATAAC[A/G]GTTTAGATAAAGAAG | 54793 |
rs369209772 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450754 | GCCTCAGCCTCCCAA[A/G]TGCTGGGATTACAGG | 54793 |
rs369216847 | snp | C/G/T | 3.61494e-05 | 0.00425128 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444380 | ATCAAAATCTAAAAA[C/G/T]CACATTAATTATCTG | 54793 |
rs369343239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427519 | ATTTTGATTTAAAAC[C/T]TTTTTCCTGTCATCC | 54793 |
rs369366881 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444881 | CCTCTTCCTCAACCC[A/G]TTACCCCAGATACTG | 54793 |
rs369413115 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450795 | CACACCCTGCTAAGT[G/T]TTTTGCTTTATTTTG | 54793 |
rs369593687 | in-del | -/TTAAAATTAAAAGTTA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449674 | TTAAATTTTAATCTA[-/TTAAAATTAAAAGTTA]AAATGCAGTTCAGTC | 54793 |
rs369637266 | snp | A/G | | | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439364 | CTCAGGACTTCGGTC[A/G]ATTAAGAAAGCTCCT | 54793 |
rs369679758 | snp | C/G | 1.64789e-05 | 0.0028704 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440652 | AACAATCCCTCAGGA[C/G]GCTTAGAATCTGTCT | 54793 |
rs369679846 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460187 | GGTACGTGATCGAAT[C/T]ACGTTCATCTTGCTG | 54793 |
rs369849147 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435456 | TAAATTGGCCATTTT[C/G]AAGTTAATGTATCGA | 54793 |
rs370026657 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455599 | TGTGCTTGCATAATT[A/G]ATATTGTCTCAAGCT | 54793 |
rs370050187 | in-del | -/ATGA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454358 | TGAATGAATGAATGA[-/ATGA]TGAATTAATCAGTAT | 54793 |
rs370173861 | snp | A/G | 1.65081e-05 | 0.00287293 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436219 | GAAATAATTGATGTA[A/G]AAGCCTGCTAATTAC | 54793 |
rs370207381 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435920 | TGCTATAGTACACAT[A/C]AGTAAAGTACCTGCC | 54793 |
rs370261370 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448488 | ATTGTGAATGTAAAC[A/G]ATGTCAATGAATTAC | 54793 |
rs370344136 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25456071 | CAGACAATTCCTGGC[A/G]AGCATATAACACAGC | 54793 |
rs370419463 | snp | A/C/G | 4.94999e-05 | 0.00497473 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460202 | CACGTTCATCTTGCT[A/C/G]GTGGGGTTATTTTTC | 54793 |
rs370638419 | snp | A/C | 0.00232588 | 0.0340225 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433440 | AGATTCGCACACTGC[A/C]AAGAAAAGAGAAAAG | 54793 |
rs370899534 | snp | C/T | 1.65378e-05 | 0.00287552 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436202 | TCATAGATTTGCTGA[C/T]AGAAATAATTGATGT | 54793 |
rs371071922 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458847 | GAAACGGCTGCGGTA[C/G]GGACGGACTGATTGG | 54793 |
rs371131065 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445810 | GGCGCATATAAAAGT[C/G]AAGAGATGAATTAGA | 54793 |
rs371172647 | snp | C/T | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439613 | ACACTCACCTTTGTC[C/T]TTAAACATGTGGGCC | 54793 |
rs371365282 | snp | A/G | 4.02763e-05 | 0.00448737 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433438 | GGAGATTCGCACACT[A/G]CAAAGAAAAGAGAAA | 54793 |
rs371368391 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25440301 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 54793 |
rs371381964 | snp | C/T | 6.58935e-05 | 0.00573955 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460361 | GAGTTGTCCTCACCC[C/T]TACAATATGTCGTCC | 54793 |
rs371393255 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431606 | ACACTGAGTACACAG[C/T]ACTAAAACCAAGGAA | 54793 |
rs371510579 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455786 | ACATGTGAAGGCCGT[C/G]CCTTCTTACAGGAGA | 54793 |
rs371525058 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447794 | TAATTGCATAAATAA[A/T]ATATGGTATATATAT | 54793 |
rs371540350 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433762 | ATCTCTATTTTTATA[A/G]ACATACCTATGCATG | 54793 |
rs371547086 | snp | C/T | 0.0021753 | 0.0329078 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458152 | TTCCGCACCGTCCGC[C/T]CTCGCCCCGACCCCC | 54793 |
rs371577984 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439482 | ATGAGGAAAAAATTG[C/T]TAAATATAAGTTTTT | 54793 |
rs371586181 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450755 | CCTCAGCCTCCCAAG[G/T]GCTGGGATTACAGGC | 54793 |
rs371661194 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459395 | GGTCTGGAAGGAGCG[C/G]CCGACGCGACGCTCG | 54793 |
rs371767123 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438531 | GGTTCTGGCACTCTA[C/T]GTCTGACCACTTTGC | 54793 |
rs371898537 | in-del | -/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448579 | TACTGCAAAGCACTT[-/G]GCACAGTGTCCTACA | 54793 |
rs371969848 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437440 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTAGATCA | 54793 |
rs371973251 | snp | C/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458071 | TGCTGTCCCCGAGCG[C/T]CCCCAGCCCGCGCAC | 54793 |
rs372081233 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439556 | GTTATAAAGTCAGCA[C/G]AGATATAAAACAGGT | 54793 |
rs372094257 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444779 | TGGAAGTAACTCTAC[C/T]GTCAGTGTTTACCCA | 54793 |
rs372171803 | in-del | -/AGAGA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448208 | CAAAGCGAGAAGAGA[-/AGAGA]CATGAATTCTGACAC | 54793 |
rs372294199 | snp | A/C | 8.23662e-05 | 0.00641688 | missense, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460368 | CCTCACCCCTACAAT[A/C]TGTCGTCCGTTTCAG | 54793 |
rs372300321 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438989 | ATCCTTTAAAGTCAC[C/T]TGTGATAGAACGTAA | 54793 |
rs372471287 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433302 | TCTGCTTCCTTCGTA[G/T]AATAGGTATTTACAG | 54793 |
rs372564816 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25435796 | CCTGTTAGTCCTATA[C/G]CTGCTAATAAGTATT | 54793 |
rs372792144 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428242 | GGCACATATTGATTA[C/T]GAAAATAGATTATCT | 54793 |
rs373074490 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444434 | CAATTATATAGACAA[C/T]AGGTTTTGCTATCAA | 54793 |
rs373075510 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428456 | TATGTCATTCTCCCA[A/G]AGGAGACACAGGTGG | 54793 |
rs373157978 | snp | C/G | 0.000148275 | 0.00860904 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433448 | ACACTGCAAAGAAAA[C/G]AGAAAAGTCCTGGTT | 54793 |
rs373189802 | snp | C/T | 1.76225e-05 | 0.00296833 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444361 | CAAAATTTAAAAAGC[C/T]ACCATCAAAATCTAA | 54793 |
rs373321741 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429577 | TAGATACTATGCCTG[A/G]TCATAAAACCAGGTA | 54793 |
rs373396453 | snp | A/C/T | 5.39214e-05 | 0.00519209 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458256 | CCTCATCGCGCTGCC[A/C/T]CCGCTGGGTCCTGAG | 54793 |
rs373577528 | snp | A/G | 3.39363e-05 | 0.0041191 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435532 | AATAAAAAAGCACAA[A/G]TTGTCACCATAACTA | 54793 |
rs373668562 | snp | A/G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448362 | AGAAAGAAAGCAGAA[A/G/T]AAAGGTTACCAAGGC | 54793 |
rs373850850 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445825 | GAAGAGATGAATTAG[A/G]TTTTTAATGTTAAAA | 54793 |
rs373979222 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444381 | TCAAAATCTAAAAAT[C/G]ACATTAATTATCTGT | 54793 |
rs374084287 | snp | C/G | 4.94189e-05 | 0.00497062 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460340 | GAAGTTGAAGGTTTA[C/G]ACAGAGAGTTGTCCT | 54793 |
rs374137868 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455181 | AGTGAGCTGAGATCA[C/T]GCCACTTCACTCCAG | 54793 |
rs374347128 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434018 | ATGGCTAAACATTAT[C/T]AACCCTGAGCAGGCA | 54793 |
rs374391720 | snp | A/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457220 | GGACAATTTCACTAT[A/T]TAAAAATTTACAGTG | 54793 |
rs374493238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448875 | AGCTGAGATCACACC[A/G]CCACACTCCAGCCTG | 54793 |
rs374526898 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430441 | TTAGATTCGCACAGG[A/G]GCGTGAACCCTATTG | 54793 |
rs374625061 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440348 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCAAAAGC | 54793 |
rs374734346 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436425 | AGGCTTACCTTTATT[C/G]CCACTTCTAGGTGTT | 54793 |
rs374734922 | snp | C/G/T | 0.00013189 | 0.00811967 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439674 | GTGCTCCTAAGAATT[C/G/T]AGGGAAAAAAATTGA | 54793 |
rs374895474 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25436286 | CAAAAATCGGACAAA[C/T]TCCTTTCGGGATATT | 54793 |
rs374980078 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434115 | TTTTGTTTTGTTTTG[C/T]TTGAGACAAAGTCTC | 54793 |
rs375041248 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441636 | GCAAAAGAAATACAA[A/G]AGTGATTAAACACAA | 54793 |
rs375063081 | in-del | -/GTGG | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429786 | CTTCTAGACAACTGA[-/GTGG]GTGGAGAAAGAAAAG | 54793 |
rs375215784 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431074 | AACCTCAAGTGATTC[A/G]CCCACCTTGGCCTCC | 54793 |
rs375271334 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444644 | ATTATGCTGAAAGGA[C/T]AGATTAAAGTCACAG | 54793 |
rs375317147 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437503 | AACACATGGTGAAAC[C/G]CTGTCTCTACTAAAA | 54793 |
rs375328781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448105 | TGCACTCCAGCCTGG[A/G]CATGATGGGACGGAA | 54793 |
rs375372945 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437169 | CTCTGGCATACAGGG[C/T]CCACATTTCCCCTTC | 54793 |
rs375375804 | snp | A/T | 1.76799e-05 | 0.00297315 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435558 | AACTAAATCGTCTGT[A/T]TGTATTAAATTTAAT | 54793 |
rs375387080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453100 | AGGCAGAGTGGCTCA[C/T]GCCTGTAATCCCAGT | 54793 |
rs375544414 | snp | A/G | 0.000164718 | 0.00907368 | missense, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460468 | ATCCTTGCACACCAG[A/G]TACTTTTAAATCACC | 54793 |
rs375861415 | snp | C/T | 0.0216662 | 0.101802 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458170 | CGCCCCGACCCCCGG[C/T]CCGCCGCGCCCCCTC | 54793 |
rs375886408 | snp | A/G | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456956 | AGATAACAGGTAGTA[A/G]CTAAGTACAGAACAG | 54793 |
rs375921238 | snp | C/G/T | 0.000148247 | 0.00860822 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460439 | TCCTCAGAAGCATGC[C/G/T]GAATTACCTCCTAAT | 54793 |
rs375931727 | snp | G/T | 3.29533e-05 | 0.00405901 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25440579 | CACACACACCTACCG[G/T]GTAGTTGTAAAGTAC | 54793 |
rs375932270 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25433683 | TAACAATAGCATGCT[C/T]ATTTTACATGAAACA | 54793 |
rs376036436 | snp | C/T | 8.24029e-05 | 0.00641831 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439560 | TAAAGTCAGCACAGA[C/T]ATAAAACAGGTAAGA | 54793 |
rs376146521 | snp | A/G | | | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456847 | TAACATAGCAGAGAT[A/G]CTGCATTAAAAAGGT | 54793 |
rs376148143 | in-del | -/GAAAT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432356 | TCAAGGAAAAGGAGA[-/GAAAT]GAAATCAACTTAGAC | 54793 |
rs376281205 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428668 | TTTAAAAAAAAAAAA[A/C]CACAAAAAAATAAGT | 54793 |
rs376282204 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451387 | TGGACATAAGCTCCA[C/G]TTAGTATATACTAAG | 54793 |
rs376286082 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454074 | GTTGTTGTTTTAGAG[A/T]TGGGATCTCACTATG | 54793 |
rs376324166 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439091 | AAGGACCACCTGCCC[A/G]TGCCTAAATCTATTT | 54793 |
rs376346101 | snp | C/T | 2.35197e-05 | 0.00342919 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433462 | AGAGAAAAGTCCTGG[C/T]TGTAAGGTTCATAAT | 54793 |
rs376430652 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440291 | TCTCGATCTCCTGAC[C/T]TCGTGATCCGCCCGC | 54793 |
rs376438089 | snp | A/G | | | upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25458472 | CTCAGCCTGCCTGGG[A/G]CCCTTCCCCCACCTC | 54793 |
rs376486097 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434391 | TCCACCACACGCAGC[C/G]AAGAGTTTTAAATTA | 54793 |
rs376643502 | snp | A/C/G | 9.8841e-05 | 0.00702935 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460363 | GTTGTCCTCACCCCT[A/C/G]CAATATGTCGTCCGT | 54793 |
rs376675418 | snp | C/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459823 | GTGGGAAGTGTATTG[C/G]GGATGGATGGGAAGG | 54793 |
rs376756319 | snp | C/T | 1.64814e-05 | 0.00287061 | synonymous-codon, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429911 | CTCTTCAAATATAGC[C/T]CCCTTCACGTTGGAC | 54793 |
rs376872670 | in-del | -/AACCC | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450352 | CTGTTCTACTAATAA[-/AACCC]CCGCCATAGGTTCAA | 54793 |
rs376953505 | snp | A/C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434426 | CATTTATCTCAAAGC[A/C/G]TTTTTGACAAACATC | 54793 |
rs376976553 | snp | A/T | 0.000387849 | 0.0139203 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433324 | TATTTACAGAAAGGA[A/T]CTCACCTTCTAAATT | 54793 |
rs376988219 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452189 | TAAATATTTACATGA[A/T]CTTATTCTTTAAAAG | 54793 |
rs377013449 | snp | G/T | 3.29984e-05 | 0.00406179 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460203 | ACGTTCATCTTGCTG[G/T]TGGGGTTATTTTTCA | 54793 |
rs377029836 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445451 | CACTGATAAAAAAAA[C/T]TCATGTTTTGCCAAT | 54793 |
rs377114101 | snp | A/C/G | 0.00016195 | 0.00899734 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444378 | CCATCAAAATCTAAA[A/C/G]ATCACATTAATTATC | 54793 |
rs377182732 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25453620 | GATCATGCCACTGCA[A/C]TCCAACCTGGGCGAC | 54793 |
rs377218221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438592 | CATGTGACCTCAAGA[C/T]TGCCAACTGCCTACC | 54793 |
rs377317200 | snp | C/T | 0.000182012 | 0.00953798 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436190 | GTAAAATTTTATTCA[C/T]AGATTTGCTGATAGA | 54793 |
rs377383774 | snp | C/T | 3.30164e-05 | 0.00406289 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460189 | TACGTGATCGAATCA[C/T]GTTCATCTTGCTGGT | 54793 |
rs377635771 | in-del | -/CTTTA | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427865 | AAAGAAATAAATTTA[-/CTTTA]ATGGTACTTTCAAAA | 54793 |
rs377654990 | snp | C/G | 0.000763819 | 0.0195276 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439456 | TAAACAAAAAATAAA[C/G]TCAGAAATGTATGAG | 54793 |
rs397724669 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439228 | AAAATCTTAAACTTA[-/A]CAAAAATGTGAGTAG | 54793 |
rs397783292 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444259 | TTTTTTTTTTTTTTT[-/T]GGCAGATAAAATTGG | 54793 |
rs397829570 | in-del | -/A | 0 | 0 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450753 | GCCTCAGCCTCCCAA[-/A]GTGCTGGGATTACAG | 54793 |
rs397891439 | in-del | -/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434452 | ACATCTTTTTTTTTT[-/T]GTCCTTAACACAAAC | 54793 |
rs397892613 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25436804 | ACTTGGTAAAAAAAA[-/A]TGTACATCCTTTACA | 54793 |
rs398086443 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443247 | CTTCCCACTAAAAAA[-/A]ATCAAGGCTTGTTGG | 54793 |
rs398112324 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443248 | TTCCCACTAAAAAAA[-/A]TCAAGGCTTGTTGGA | 54793 |
rs398112325 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25443478 | ATAACAATAAAAAAA[-/A]CCTTAATTGATCATT | 54793 |
rs527294524 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437416 | GGCCGGGCTCACACC[G/T]GTAATCCCAGCACTT | 54793 |
rs527351251 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429347 | ATACGGTGTGACAGG[C/T]ATTTAAAGAGGGGAG | 54793 |
rs527622137 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459146 | GGACTGGAGAAGGGG[G/T]AGGTGGCGGAGTGAT | 54793 |
rs527639728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453175 | CAGCCTGACCAACAT[A/G]GTGAAACCCCATCTC | 54793 |
rs527658183 | snp | A/T | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457008 | ATGAGAAATGTAAAC[A/T]TCGTGAACATATTTT | 54793 |
rs527703436 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453632 | GCACTCCAACCTGGG[C/T]GACAGAGTGAGACTC | 54793 |
rs527704394 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446316 | CCCATAAGTTATAAA[C/G]TACCACACTAGAACA | 54793 |
rs527778167 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25432675 | GTAGTTTAACTTAAA[A/G]ATATAGTTATCTACC | 54793 |
rs527790792 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459248 | GGAGGAGGCTGCCGG[A/G]CAGAGCGCAGGCCAG | 54793 |
rs527812457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446823 | AAAGATAACTTCTCA[C/T]CTCATTTATTTAATT | 54793 |
rs527888199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430860 | TTTTTTTTTTGAAAC[A/G]GAGTTTTGCTCTTGT | 54793 |
rs527954953 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431530 | GTCAGCAGCTCTCCC[C/T]TCAATAGTCAACCTG | 54793 |
rs527977538 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457160 | AATTTTCGGAGCATG[-/T]TTTACTCTACACTGA | 54793 |
rs528029501 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455791 | TGAAGGCCGTCCCTT[C/G]TTACAGGAGACCTGA | 54793 |
rs528107004 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456472 | GGGAGAGAAAACACT[A/G]CCAACGTCTTAGAAT | 54793 |
rs528128854 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450354 | TGTTCTACTAATAAC[C/T]GCCATAGGTTCAAAT | 54793 |
rs528139591 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434972 | TCAAAATATCTGTCA[A/G]ATACTTCTTGAGCAG | 54793 |
rs528219415 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449864 | AACTATTTTAATTCT[A/G]TTAGGCTTTCCCATG | 54793 |
rs528255794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442555 | AATGGCATCTTGCCA[C/T]TGGAAGATGTCACCG | 54793 |
rs528317323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443114 | CCTATAACATACATT[A/G]TATACAAATTTTATC | 54793 |
rs528612501 | in-del | -/TT | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438880 | GCATGATTTGCCCTC[-/TT]GACTACTCTAGTTCT | 54793 |
rs528628336 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449582 | GGGTCTATTGTCTTC[C/T]GATGAAAATAAAGGC | 54793 |
rs528650282 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457960 | AGACCCGGAGCCCCC[A/G]GGCCGAACCGCGCCG | 54793 |
rs528764498 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451881 | TGTATTTGAATTCAA[C/T]TTTTATTGCCACTTT | 54793 |
rs528810897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452496 | CCTGCAGCATCTGAA[A/C]CACATTTCACCTGCA | 54793 |
rs528880801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430704 | CCAAAACCAGCCCCC[A/G]ACTCTGATCTGTGAA | 54793 |
rs528990845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459976 | GTTTATAACAAAAAG[A/G]ATAAATATTTGAGAT | 54793 |
rs529003818 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444988 | TTTTATTTCCTATAG[G/T]ACATCACAGGACACG | 54793 |
rs529055675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453924 | AGTGGGCCCTCACTA[A/G]GTTCTTATTAATGTT | 54793 |
rs529197492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447956 | ACATGGTGAAACATG[A/G]TCTCTACAAAAAAAT | 54793 |
rs529245417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448389 | AGGCATAGATGGGAA[G/T]GGAGACTTATTTCTT | 54793 |
rs529396102 | in-del | -/AATA | 0.0209421 | 0.100162 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455245 | ATAATAATAATAAAT[-/AATA]AATAAATAAATAAAA | 54793 |
rs529403884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432753 | GGAAATTAATCTAAA[A/T]TCTTGTCTCTCAACG | 54793 |
rs529681099 | snp | A/T | 3.30759e-05 | 0.00406655 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436201 | TTCATAGATTTGCTG[A/T]TAGAAATAATTGATG | 54793 |
rs529854577 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429193 | TGACAGTGATGTACA[A/G]TGATGTCTTTCTTTC | 54793 |
rs529893715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427833 | TTTTTAAAAGAATGA[C/T]AAAAATAATCATGTT | 54793 |
rs529990616 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437308 | CTAAGTAAAGCAGAA[-/C]TCTTAGGGAATGCAG | 54793 |
rs530074170 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458681 | ACGGCGGCTTCCAGC[A/G]TTACTGAGCAGGCGC | 54793 |
rs530293091 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441507 | AACATGCTAAAAGAA[A/G]TTTATACAAGGTATA | 54793 |
rs530344917 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430112 | TCCGGAAAACTGATG[A/G]TACACCACCCTAAAT | 54793 |
rs530444828 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451981 | CTGGATCCTAAAGGT[C/T]CAATAAAAAAATTAA | 54793 |
rs530454281 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438904 | CTAGTTCTCACATAA[G/T]GTGGGGAATATCCAG | 54793 |
rs530608183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455054 | AACATGGTGAAAACC[A/G]TCTCTACTAAAAATA | 54793 |
rs530673070 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448607 | ACACACAGCAGGCTT[G/T]CCATAAATAATTAAA | 54793 |
rs530685702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449219 | TGAAAAGAGGGTAAG[A/C]AGCACAAGCACCTCT | 54793 |
rs530746344 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433934 | TCAGAATACAAAAGC[C/T]AGCATTTAAAGGCAT | 54793 |
rs530848005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453259 | CTACTCAGGAGGCTG[A/C]GGCAGGAGAATCGCT | 54793 |
rs530859164 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442377 | GAATAAAATGCAGTA[A/G]CATATTTAAGATATT | 54793 |
rs530930541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434726 | CCAAAAGCAAGATGG[C/T]ATTAATTCAAAAGAC | 54793 |
rs530982073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456583 | ACATAAACATATTTA[C/T]ATTTAATTATTTGAG | 54793 |
rs531102120 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449235 | AGCACAAGCACCTCT[C/T]TCCCAATTCAATGTT | 54793 |
rs531154225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450875 | GGGGGAAGTTTTAAT[C/T]TATTTTAAGGTCTCC | 54793 |
rs531200777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438071 | CTGCTTTTTGAACAC[C/T]TGAACAAATAAATGG | 54793 |
rs531211340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430083 | TGTTCTTATACAATA[A/C]AACTCAGTTAATTTC | 54793 |
rs531379011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444231 | CCCCATTTAAAATAA[C/T]TGTCATTCCATCTTT | 54793 |
rs531493245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459886 | GAATGAATAAGATCT[A/G]GTATTTGCTAGCACA | 54793 |
rs531559815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446941 | AATCAAGCAGTCTGA[C/T]ATATGTGCAAGATAC | 54793 |
rs531559829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454452 | TGTGTTCAAGACGTA[C/T]AGAAACTCTGCACTG | 54793 |
rs531617932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447893 | GCACTTTGAGAGGCT[A/G]TGGCAGGTGGATCGC | 54793 |
rs531724195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437096 | TGAAGACCAAACTCT[A/G]TGGTCAACAATCCAA | 54793 |
rs531808702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431742 | CTGCTACTCTGCTAC[C/T]GAGAGCTATCAAGAT | 54793 |
rs531992893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450738 | ACCTCGTGATCCAAC[C/T]GCCTCAGCCTCCCAA | 54793 |
rs532028146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442666 | CTGGAGGTAAGTGTA[C/T]GCTTGAAGAAGTAAA | 54793 |
rs532213922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436635 | GGTTTGCCACAAGTA[C/T]CTTTTACATACTGAA | 54793 |
rs532486964 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452207 | TATTCTTTAAAAGAT[A/G]AGATAATTTAAAAAA | 54793 |
rs532638619 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458099 | CACGCCCACCTCCCA[C/G]CCCCTCTACCCAACT | 54793 |
rs532692836 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458591 | TAACCTAGCCGGGAC[A/G]GAGGGAGGGAAGAGA | 54793 |
rs532700681 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451710 | CCATGCCTAGTACGA[C/T]TGGCTAGTTTTAATT | 54793 |
rs532704794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452545 | CTACCCCACCCCAGA[C/T]CTACTGAATATTAAT | 54793 |
rs532715205 | in-del | -/A | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454423 | TGAATATTCTGAAGT[-/A]AAAAAAAGCACTCTG | 54793 |
rs532721956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446018 | ATTCTAGGTAAACAC[A/T]TGCCAAAATCCTGTA | 54793 |
rs532867927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437570 | GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 54793 |
rs532920509 | in-del | -/C | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428850 | TTGCCTTTTAGCAGG[-/C]CAACTCTACCATATT | 54793 |
rs533067036 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449043 | TGGGACAAAGCGAAG[C/T]GAAATACAGTACCTA | 54793 |
rs533098065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454534 | TTTCAATTTCCTTAA[C/T]GCCAACTCTTACAGG | 54793 |
rs533106709 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440912 | GAAAGAAAAAGCAGA[C/G]AGAAGCAACAGGGTA | 54793 |
rs533110653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454977 | ACGCCTGTAATCCTA[A/G]CACTTTGGGAAGCCA | 54793 |
rs533485932 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456545 | TTTATCTAGTACTCT[A/C]CAGTTTGGATTTTTA | 54793 |
rs533502231 | snp | C/T | | | upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25458565 | GCACCCAGTATCGGG[C/T]GGGCTCTGGCTAACC | 54793 |
rs533546409 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427921 | AGTTATACTGTATTT[C/G]CTTTGCTACCCAGAA | 54793 |
rs533624772 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434188 | CACTGCAATCTCTGC[C/T]TCCCAAGTTCAAGTG | 54793 |
rs533703879 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458190 | CGCGCCCCCTCACGC[C/T]CCCGTTACCTTTCCG | 54793 |
rs533989579 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437332 | AATGCAGCCAGGATA[C/T]GTTTCCAATTCTAGG | 54793 |
rs534134395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444797 | CAGTGTTTACCCACT[A/G]CACATCCACCATACA | 54793 |
rs534154278 | snp | C/T | | | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427599 | TTAATGGAAGTTTTA[C/T]TATTTTAACGGTTTC | 54793 |
rs534203262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437662 | CAGCCTGGGTGACAC[A/G]GCAAGACTCCATCTC | 54793 |
rs534318710 | snp | A/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429687 | AGAATATGGAAAAAA[A/T]GTCAGTTTTTTCCCT | 54793 |
rs534380358 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430351 | GTAGATGAAGCTTCA[A/T]CTGTATTTACAGCCA | 54793 |
rs534496860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459543 | CTTTGTTCGGCTTAC[C/T]CTGCAGCACAGAATT | 54793 |
rs534550286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440434 | TTTTTTCTTCAAAAA[A/C]AGTTATAAAAAATGG | 54793 |
rs534564586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448662 | GCTCACGCCTGTAAA[A/G]TCTGCACTATGGGAG | 54793 |
rs534616647 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441092 | TAAAACCAAATGGCC[A/C/G]AAACTCCCTTCCATG | 54793 |
rs534673197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456139 | CAGGCTTCATAGTCT[C/T]ACAGTCTGGTAACTA | 54793 |
rs534773196 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25448052 | AGGATCACTTGAGCC[C/T]GCCAATTCAAGGCTG | 54793 |
rs534783507 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449687 | TATTAAAATTAAAAG[C/T]TAAAATGCAGTTCAG | 54793 |
rs534860437 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442136 | ACAAAATAAAAATGT[C/T]AACTTCAAGAGAACT | 54793 |
rs534898069 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454816 | TGTTAGAAAGTACAT[A/G]TTTTCCCAAATGATG | 54793 |
rs534901964 | snp | A/C/T | 6.60529e-05 | 0.00574656 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25435436 | TGTGCAAGATTACAG[A/C/T]GGCTTAAATTGGCCA | 54793 |
rs535088463 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457618 | GCGGCGGCGGGGCGT[A/G]GGGGCTTGAGGCATC | 54793 |
rs535148007 | snp | A/G | 0.000625782 | 0.0176777 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460287 | AACCAAGGAGTCTGC[A/G]ATGAATAATGCTGGT | 54793 |
rs535180637 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459328 | GGGTTCGAAGAGCGG[C/T]TCCCGGCTGCGGGTG | 54793 |
rs535226173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446461 | GAACATAAGAAATCA[C/T]CTCTGACCAAAACAA | 54793 |
rs535406997 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441526 | ATACAAGGTATAAAA[C/T]AACAATATAAACCAG | 54793 |
rs535407307 | snp | C/T | 6.68606e-05 | 0.00578151 | missense, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25439399 | GATCTTGCTTATTTC[C/T]CCAGACACCTGTGTC | 54793 |
rs535440986 | in-del | -/A | 0.157972 | 0.232445 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448918 | GACTCCTTCTCCAAG[-/A]AAAAAAAAAAAGAAA | 54793 |
rs535559017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460128 | AACCTGTGACGTGTG[A/T]TTCTATGCCAGTATG | 54793 |
rs535755687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454726 | ATGTTTCTGACCACA[C/T]ACCCCATTGGTAACA | 54793 |
rs535767285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430546 | CCAACACCCCCAGAT[G/T]GGACTGTCTAGTTGC | 54793 |
rs535922700 | snp | A/C | | | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457681 | GCCCCCATTTTAAAA[A/C]TCCTGTCTGCGACCT | 54793 |
rs536126362 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439030 | AATATAAAGTTGATG[C/T]GTATGGCTTACATAT | 54793 |
rs536163418 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458158 | ACCGTCCGCCCTCGC[C/T]CCGACCCCCGGCCCG | 54793 |
rs536415173 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430894 | CCAGGCTGGAGTGCA[A/G]TCTCGGCTCACTGCA | 54793 |
rs536470791 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429622 | ATTCAAAAGGCAGCA[A/G]TATCTAGTTTCCCTA | 54793 |
rs536542776 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457370 | TGTCTGCCTCGAACA[A/G]TGAAAATTTCCCAAA | 54793 |
rs536588054 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446871 | GATTTTAGCATCTAA[C/G]ATTTAAGAACAGAGC | 54793 |
rs536619568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443858 | CACCTGTGTGTGTGG[C/T]TGATACCAAGTCATT | 54793 |
rs536701830 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428043 | AACAAACACTTTATA[G/T]CATTTATTAATGCAG | 54793 |
rs536801753 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437209 | CCAAAGATTATGCCA[G/T]TCCGTTCGGATATAT | 54793 |
rs536804784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437594 | GAGGCAGGAGAATGG[C/T]GTGAATCCAGGAGGC | 54793 |
rs536815021 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428662 | AATTTGTTTAAAAAA[A/C]AAAAACCACAAAAAA | 54793 |
rs537014354 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454649 | AGTTTTAAAAAACAA[A/T]AACAAAAAAAACCCT | 54793 |
rs537206276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440982 | TGACTTCATTGCTTA[A/G]TAAGTCTAGCTGAAA | 54793 |
rs537211400 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445562 | TTTGTTAAGCATCTT[C/T]CTGCTCCAAAATTCT | 54793 |
rs537218677 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449532 | ACTAACTTGAATTGT[C/T]GTCTACTTCCATATG | 54793 |
rs537329820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450131 | AATTGAATTCAACTT[C/T]TATTGCCACTTAAAT | 54793 |
rs537335648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441758 | ATCCTCTGGGAGGCC[A/G]AGGCGGGTGGATTGC | 54793 |
rs537392749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434452 | ACATCTTTTTTTTTT[C/T]GTCCTTAACACAAAC | 54793 |
rs537430987 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437070 | TGGGAAGAATAATAC[A/G]ATCTTTTCTGTGAAG | 54793 |
rs537546442 | snp | C/T | 1.79544e-05 | 0.00299615 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458277 | GGGTCCTGAGTGAGC[C/T]GCCACCCTCCCACCT | 54793 |
rs537555001 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458747 | GGGCGGGGTCTGGGG[A/G]AAGGAGGTGGAGCGC | 54793 |
rs537559467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456066 | ATACACAGACAATTC[C/T]TGGCGAGCATATAAC | 54793 |
rs537625431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452780 | AATATCATGGTAGTA[C/T]TTGTATAACATGTAC | 54793 |
rs537747991 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458459 | CGCCCCTAGGCTCCT[C/T]AGCCTGCCTGGGGCC | 54793 |
rs537751639 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447591 | ATGGAAAAAGCTGCT[C/T]GATAACATACGAGTG | 54793 |
rs537796463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446428 | ACTTGGTGCCTAATA[C/T]TGCCGACTCCTCAAC | 54793 |
rs537808167 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438479 | CAAAAACATGTCACA[A/T]AAAATTTTAGATACC | 54793 |
rs538184272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437819 | CACCATTGCACTCCA[G/T]CCTGGGTGACAGAGC | 54793 |
rs538370548 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431010 | AATTTTTTCTATTTT[A/T]AGTAGAGACGGGGTT | 54793 |
rs538508493 | snp | A/G | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460133 | GTGACGTGTGTTTCT[A/G]TGCCAGTATGGACTG | 54793 |
rs538545070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454192 | GTGCCTGCCCCCAAC[A/G]TGTTTCTGACCTAAT | 54793 |
rs538582334 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441711 | TTGAAAAATTAAAAA[G/T]AAATGGTCAGACGTG | 54793 |
rs538655309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434297 | TAGAGACGGGGTTTC[A/G]CCATGTTGGCTAAGA | 54793 |
rs538815895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444423 | ACTATTCCTTACAAT[C/T]ATATAGACAATAGGT | 54793 |
rs538943625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456911 | ATTTTGAACATACTA[A/T]ATCTTTCTTAGAGTA | 54793 |
rs538968055 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438213 | ACAAAATGCTATCAA[A/T]AATTTGAAGAAAAAT | 54793 |
rs539119306 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451037 | AATCTTATAGTTCTA[C/G]AAATTTGAAAATTTC | 54793 |
rs539171655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443683 | GAACTACTTCCACTC[A/G]CCAAATGCAATTAGT | 54793 |
rs539172016 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450531 | GCAATTCTAAAGCAG[G/T]CTGGGCATGGTGGCT | 54793 |
rs539182241 | snp | A/G | 1.64917e-05 | 0.00287151 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436378 | TTTTGGGAGATAGCT[A/G]CAATGAATGTAACAC | 54793 |
rs539403314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460045 | TTGCATGCCTGTATC[A/C]AAATATTTCATGTAC | 54793 |
rs539403614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453383 | GGTGAGGGCCGGGCA[C/T]GGTGGCTCAAGCCTG | 54793 |
rs539617577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455121 | TCCCAGCTAAGCAAG[A/C]GGCTGAGTTAGGAGA | 54793 |
rs539638731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440347 | ACAGGCGTGAGCCAC[A/C]GCGCCCAGCCAAAAG | 54793 |
rs539722099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455912 | AGATATAAACAAAAG[A/G]TATATTTCTTCCTGA | 54793 |
rs539729479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448717 | CTCAGGAGTTCGAGA[C/T]CAGCTTGGGCAACAC | 54793 |
rs539804908 | in-del | -/A | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429681 | AAAATCAGAATATGG[-/A]AAAAAAGTCAGTTTT | 54793 |
rs539866527 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455818 | CTGAGACCAGCTGAA[A/T]GTTCAGTGACTGGAG | 54793 |
rs539868512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456516 | GAGCAGTGAAGATCA[C/T]GGCTTTGCTTCTTTT | 54793 |
rs540119716 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25445408 | ACTTTGTATATCATT[A/G]TAGGTTAAAGCATCA | 54793 |
rs540326239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450650 | AAAACCGTGCCACCA[C/T]GCCCAGCTAATTTTT | 54793 |
rs540389615 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443145 | TCTACCTATATATTT[C/T]CAATTCTGTCCACCA | 54793 |
rs540511404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435984 | ACTGACTTTTAAAAA[A/C]CTGCTGCAATTTCTA | 54793 |
rs540571685 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452953 | AGGAGGACTGCTTGA[A/G]GCCAGGAGTTTGAGA | 54793 |
rs540576478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436623 | CAGATCTGAACAGGT[C/T]TGCCACAAGTATCTT | 54793 |
rs540588668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437216 | TTATGCCATTCCGTT[C/T]GGATATATATCCCTG | 54793 |
rs540588964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427609 | TTTTACTATTTTAAC[A/G]GTTTCTTCCCTCCTT | 54793 |
rs540620541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431377 | GAACAGTGTAACCAC[C/T]GCAATTTGAAGCTAT | 54793 |
rs540875028 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455150 | GAATCGCTTGAACCT[-/G]GGGGGCAGAGGTTGC | 54793 |
rs540916574 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458836 | GGCCCAGCTAGGAAA[C/T]GGCTGCGGTAGGGAC | 54793 |
rs540956088 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454942 | CTTTAAACATTAAAA[A/T]AAGCCGGGCATGGTG | 54793 |
rs541041017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432417 | AGTTTTACCAGCCAA[C/T]TACTTTGTTTTGATT | 54793 |
rs541107922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441212 | GATGAAAGTTAAGAG[A/G]TTTAATAGACCAGAA | 54793 |
rs541169586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433698 | CATTTTACATGAAAC[A/G]TAACGGTTTAGATAA | 54793 |
rs541236061 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25450363 | AATAACCGCCATAGG[C/T]TCAAATGGTACATTA | 54793 |
rs541318721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455432 | GAGGCTGATTATTAA[C/T]AGCAATTAATAAATA | 54793 |
rs541566430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445883 | AGTACCACAAAGAAG[A/G]AATTCCTCATAGCTA | 54793 |
rs541576215 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437961 | GTTTTAAAGCATATA[A/T]TTACTTGGGGCAACC | 54793 |
rs541732118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445492 | AACTCAGGCAAAGCA[A/G]TGATAACATAAGTGG | 54793 |
rs541958985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453487 | GGTGAAACCCTGTCT[C/G]TACTAAAAACACAAA | 54793 |
rs541961738 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429316 | GAGTCTTAGGGAGTC[G/T]GATCTCACCATATTC | 54793 |
rs542232146 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25451707 | ACACCATGCCTAGTA[C/T]GATTGGCTAGTTTTA | 54793 |
rs542235029 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458975 | AAGAGAAGCGTTACT[C/T]CGCGAGACTCTCCTG | 54793 |
rs542339432 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428935 | TGGCCCTATGTAAAC[A/T]ATTTGGTATTTGAAT | 54793 |
rs542367735 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431915 | ATTTAAAAATCAATT[C/T]CTCATTTGCACTAGC | 54793 |
rs542462912 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459008 | AAGTAGTCCCCGAGG[A/T]CACAAGGCAGTGGCA | 54793 |
rs542490332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447392 | GCTCTGTCTCCCCGC[C/T]AAAAAAAGAAAAATA | 54793 |
rs542583610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439845 | AGATCCCTTCTAATA[A/G]GGTACTTCCTTTGAT | 54793 |
rs542711456 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456432 | GTCAAATAAGAATAA[A/T]TATAAATTTTTTTAA | 54793 |
rs542740540 | snp | A/C | 0.00294423 | 0.038255 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436528 | AACCTAATTTAGTGA[A/C]TGTATTACATTCATT | 54793 |
rs542810822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449845 | AATGAAGAAAAAAAA[A/C]CACAACTATTTTAAT | 54793 |
rs542922895 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25450536 | TCTAAAGCAGTCTGG[G/T]CATGGTGGCTCAAGC | 54793 |
rs542955323 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458322 | CTTTTTCTCCTCCCG[A/C]CCTTCCCCTCCCTCC | 54793 |
rs542984361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443102 | TAAACTTTATATCCT[A/G]TAACATACATTATAT | 54793 |
rs543024724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438753 | TAGATAGGGTCAAGA[A/G]TGCTTTTAACACTCA | 54793 |
rs543208672 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446754 | GGTTCATCCTTAGAA[C/T]AGGAGTGTGCTGGTA | 54793 |
rs543297680 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457840 | CCCGCAGGCGGGAGC[G/T]GGGTCTCGGGGAGAG | 54793 |
rs543312002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451384 | TCATGGACATAAGCT[C/G]CAGTTAGTATATACT | 54793 |
rs543507707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448346 | ACAGGCAAATTCATA[A/G]AGAAAGAAAGCAGAA | 54793 |
rs543519579 | snp | A/G | 0.000132251 | 0.00813069 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440676 | TCTGTCTGAGGATCT[A/G]GAGATGACATGTAGA | 54793 |
rs543553198 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431306 | AGCAAGGAACTGCCC[C/T]TCTTTTTAAAGCCCC | 54793 |
rs543743685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448643 | AGTAGGGCTGGGCGC[A/G]GTGGCTCACGCCTGT | 54793 |
rs543832684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454856 | AGTGACTCAGACTAT[C/G]AATTAGCCACTAAGA | 54793 |
rs543898254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451338 | TTTATATAACTCTTT[C/T]GAGAAAGAGGAGCAA | 54793 |
rs544302259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444117 | AATAAACTACGATCA[C/T]ATAGTAAAAAATTTA | 54793 |
rs544310435 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434077 | GTAAAATGGTAGAAA[-/AT]ATATGTTTTAAGACT | 54793 |
rs544370180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436724 | TTCAGAAATCTGTCT[C/T]ATAGGAGAATAAATT | 54793 |
rs544562849 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428962 | GAATTAAATGAATAT[C/T]AATGATGCACCTTGG | 54793 |
rs544631288 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449119 | ATGAAGAGAGTAAAG[A/T]CAGAGAAGAGAGAAG | 54793 |
rs544825395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459658 | TCTTGAGAGGGGTAC[C/T]CTTATGATTCAGGTT | 54793 |
rs544915151 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453468 | AGACCAGCCTGGCCA[A/C]TATGGTGAAACCCTG | 54793 |
rs544917001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446047 | TACTCTTAACAGTGA[C/T]TAAATTACTGCTTAA | 54793 |
rs544929136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446581 | TCAACTTGAGTCAAC[A/C]TACTGATGCTTCTGT | 54793 |
rs545022997 | snp | A/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25446392 | AACAGTGCCCCCTTT[A/T]CTTCCATGACTCATT | 54793 |
rs545155576 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442947 | CCCTGAAAGTCAGGA[C/G]TATTGATATAGAAAA | 54793 |
rs545217246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435609 | TTTTTTTTAGAAGCA[A/G]TTGGCAGTTCAGTCA | 54793 |
rs545264409 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451290 | ATTAAGTTACGGAGA[-/G]AAGTTGCAAACAGAC | 54793 |
rs545321337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456209 | GAGATTATTCTTATA[A/G]CCAGGAAACAAAAGC | 54793 |
rs545356824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442240 | CCAGAACAACTCAGA[A/G]CACCAATAAATATTC | 54793 |
rs545384249 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448084 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 54793 |
rs545547621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430583 | ACAAACTCAGGGCTC[C/G]CACTGATTCTACATT | 54793 |
rs545889626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454437 | GTAAAAAAAGCACTC[C/T]GTGTTCAAGACGTAT | 54793 |
rs545990921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447655 | AACTTTTTTCTCTTG[A/G]ATCAGAAGGATGAAA | 54793 |
rs546250275 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25431038 | GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA | 54793 |
rs546368712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449875 | TTCTATTAGGCTTTC[C/T]CATGACATAGGAACC | 54793 |
rs546784614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25434883 | CATATATATAAATAT[A/G]CACATATATGTAGAG | 54793 |
rs546788549 | in-del | -/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452113 | CAAAACCACTAATCA[-/C]CACTAGTAACTAAAT | 54793 |
rs546800750 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449632 | CTGTGCTGTCCAGTG[C/T]GGAAGCCACTAGCTT | 54793 |
rs546896856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436894 | TACATTTGGGTTCCA[G/T]TATCTTTCAAATGAG | 54793 |
rs546912586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451581 | TTTATTGAGAAGCAT[A/G]TCTATTAAAGTTCAT | 54793 |
rs546944169 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455057 | ATGGTGAAAACCGTC[C/T]CTACTAAAAATACAA | 54793 |
rs546975948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444406 | ATCTGTTGCTTATAG[A/G]AACTATTCCTTACAA | 54793 |
rs547075151 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457219 | TGGACAATTTCACTA[C/T]TTAAAAATTTACAGT | 54793 |
rs547140431 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457993 | CCCCAGGCAGCTGAG[A/G]CACTGAAGGGCAGGC | 54793 |
rs547190449 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453942 | TCTTATTAATGTTTA[C/G]CCTTCAGAGGCAGAG | 54793 |
rs547256582 | in-del | -/TACCT | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25444028 | TTCTAAGATCAAAAC[-/TACCT]TACTATGTTACAGTT | 54793 |
rs547352721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431917 | TTAAAAATCAATTTC[C/T]CATTTGCACTAGCCA | 54793 |
rs547466525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432917 | GTAGTCTCCTAAATA[G/T]ACAAGTAAACAAAGT | 54793 |
rs547467453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25460037 | ATTACGAATTGCATG[C/T]CTGTATCAAAATATT | 54793 |
rs547528093 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25460403 | TGCCTCTTTCATTTT[A/G]GGAACTGGGAAGATT | 54793 |
rs547553072 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25447116 | AACTAGGTAAGGGTC[A/G]GGCGCAGTGGTTCAT | 54793 |
rs547596784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454509 | CTGCATGCAGATGTG[C/G]AAGTCCCCATTTCAA | 54793 |
rs547659910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448047 | ATGGGAGGATCACTT[A/G]AGCCTGCCAATTCAA | 54793 |
rs547736865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449779 | AGCACAAATTTCCAT[C/T]ATCTCAGTAGTTCTA | 54793 |
rs547750773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444192 | TACAGCCATAAGATC[A/T]TTTTTAATGTTTAAG | 54793 |
rs547857065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436823 | ACATCCTTTACATGA[C/T]TTGGTATATTTACTT | 54793 |
rs547987368 | snp | A/C | | | intron-variant, upstream-variant-2KB | CDCA2, KCTD9 | GRCh38.p7 | 8:25459882 | CAAAGAATGAATAAG[A/C]TCTAGTATTTGCTAG | 54793 |
rs548018654 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25427844 | ATGATAAAAATAATC[A/C]TGTTTAAAGAAATAA | 54793 |
rs548093720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455812 | GGAGACCTGAGACCA[A/G]CTGAATGTTCAGTGA | 54793 |
rs548111767 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25437498 | TGGCCAACACATGGT[A/G]AAACCCTGTCTCTAC | 54793 |
rs548203704 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458697 | TTACTGAGCAGGCGC[A/G]CCCTCTAGTTTAGGT | 54793 |
rs548360318 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25434176 | GCTGTCTCAGCTCAC[C/T]GCAATCTCTGCCTCC | 54793 |
rs548416158 | snp | C/T | 0.00122986 | 0.0247673 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458167 | CCTCGCCCCGACCCC[C/T]GGCCCGCCGCGCCCC | 54793 |
rs548519107 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430171 | CCTCTAGTTCAGGCT[A/G]ATCACCATAAATATG | 54793 |
rs548620027 | in-del | -/CACA | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430840 | ACACACACACACACA[-/CACA]ATTTTTTTTTTGAAA | 54793 |
rs548628876 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452115 | AAACCACTAATCACC[A/G]CTAGTAACTAAATAC | 54793 |
rs548652079 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453154 | GATCAGGAGGTCAGC[C/T]GAGACCAGCCTGACC | 54793 |
rs548689481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25445465 | ACTCATGTTTTGCCA[A/G]TTAAATGGTATAACT | 54793 |
rs548767175 | snp | A/C | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441781 | TGGATTGCTTGAGCT[A/C]AGGAGTTCGAGACCA | 54793 |
rs548993735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455055 | ACATGGTGAAAACCG[C/T]CTCTACTAAAAATAC | 54793 |
rs549053428 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25430610 | CATTATGGTGAGTTA[C/T]ATAATTATTTCATTA | 54793 |
rs549100949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440995 | TAATAAGTCTAGCTG[A/G]AAACAACAGATTGAG | 54793 |
rs549103271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449248 | CTTTCCCAATTCAAT[A/G]TTCTTGGCATAGTTG | 54793 |
rs549271445 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25443460 | TTTTTAAATCCATGA[C/G]TTAATAACAATAAAA | 54793 |
rs549470473 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KCTD9, CDCA2 | GRCh38.p7 | 8:25456749 | CCAACTCAGTTAATT[A/T]TTGACAACCAAATTG | 54793 |
rs549629035 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459287 | CAGGCTGTGAGTCCA[A/G]GTCAGCCGTCGGGAC | 54793 |
rs549639136 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441415 | AAAAGTGTTAAAATA[A/G]TAATTGTCCTTATAG | 54793 |
rs549712737 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25455958 | CTTGGACACTGTCTG[G/T]GGTGTGTCATCTCAC | 54793 |
rs549925854 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433623 | GGGAACATTTGAAAG[-/A]AAAAATTTTTTTAAA | 54793 |
rs549995351 | snp | C/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25449460 | ACCTGCCTGTATTAT[C/G]CTTAATACTTAATGT | 54793 |
rs550246227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440159 | CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT | 54793 |
rs550744284 | snp | A/C | 0.000337724 | 0.0129903 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25458149 | CGGTTCCGCACCGTC[A/C]GCCCTCGCCCCGACC | 54793 |
rs550851294 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KCTD9 | GRCh38.p7 | 8:25436611 | TTTTAAATGGAGCAG[A/T]TCTGAACAGGTTTGC | 54793 |
rs550880871 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430548 | AACACCCCCAGATGG[A/G]ACTGTCTAGTTGCAA | 54793 |
rs551001908 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429550 | ATCATGCCTATTTAA[A/G]AGCAAATATAATAGA | 54793 |
rs551009939 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458620 | GACGCTGAAGGCTAG[C/T]AGACGGGAAGGGGCA | 54793 |
rs551053985 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451726 | TGGCTAGTTTTAATT[A/T]ACCTTTAAACACCAT | 54793 |
rs551058973 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | KCTD9 | GRCh38.p7 | 8:25437721 | GGCATCATGGTGTGT[-/G]CCTGTAATCCCATCT | 54793 |
rs551115528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452612 | CCTCCTCCTCCAAGT[A/G]ACTCTGATGCATGCT | 54793 |
rs551117376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444435 | AATTATATAGACAAT[A/G]GGTTTTGCTATCAAT | 54793 |
rs551266426 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438087 | TGAACAAATAAATGG[G/T]TGAGAAACATGAAAA | 54793 |
rs551332246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25433786 | ATGCATGACAATGAA[A/C]CAGTCAAAATGTATG | 54793 |
rs551370513 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25447331 | GGCAGAGGTTGCAGT[G/T]AGCCAAGGTTGCACC | 54793 |
rs551392698 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25441252 | AAATGAGTTCTGTGT[A/T]TTTTAAACACTTCAC | 54793 |
rs551453137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454563 | GGGAATATTAAAAAG[A/C]ATAACGAAAATGTTG | 54793 |
rs551522055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KCTD9 | GRCh38.p7 | 8:25455010 | GCAGGTGGATCACAT[A/G]AGGTCAAGAGTTCAG | 54793 |
rs551839437 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429387 | AAGCTATTTATAAAC[C/G]TGAACAACCTTTTCC | 54793 |
rs551968059 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25438063 | AGAGAGCTCTGCTTT[C/T]TGAACACTTGAACAA | 54793 |
rs552014817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25452738 | CAAAATATAAAGAAA[A/G]TAAACAACCTAATGT | 54793 |
rs552077992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453183 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 54793 |
rs552105061 | in-del | -/T | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25456274 | AGATATTCCAACTGG[-/T]GGATGGGAAATCAAA | 54793 |
rs552190078 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KCTD9 | GRCh38.p7 | 8:25453673 | AAAAAAAAAAAAGGT[A/G]ATTTAGTTATGCATA | 54793 |
rs552326521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446385 | GGTTCTTAACAGTGC[C/T]CCCTTTTCTTCCATG | 54793 |
rs552383918 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KCTD9 | GRCh38.p7 | 8:25438416 | GAAACTGTAAGCCAG[C/G]AGTCCTCAGGCTGAT | 54793 |
rs552599784 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454093 | GATCTCACTATGTTG[C/T]CCAGGCTGGTCTTGA | 54793 |
rs552648283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25439004 | TTGTGATAGAACGTA[A/C]ATCAATTTAGAATAT | 54793 |
rs552689067 | snp | G/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25442397 | TTTAAGATATTCAAA[G/T]AAAAATAATGTGAAC | 54793 |
rs552711291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430434 | AGGGGCATTAGATTC[A/G]CACAGGAGCGTGAAC | 54793 |
rs552889052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KCTD9 | GRCh38.p7 | 8:25431542 | CCCCTCAATAGTCAA[C/T]CTGATCAGTCTTTGC | 54793 |
rs553038268 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25432444 | GATTTCAATAAATTT[G/T]GCATGAGATGCTTAG | 54793 |
rs553154932 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KCTD9 | GRCh38.p7 | 8:25442809 | AAAACATTTAACTGT[C/T]TTTAGTAATTATATT | 54793 |
rs553193798 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25452955 | GAGGACTGCTTGAGG[C/T]CAGGAGTTTGAGACC | 54793 |
rs553228443 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CDCA2, KCTD9 | GRCh38.p7 | 8:25458780 | AAAGGGACCCAAGCA[C/T]CAGTCAGCCCCTCCT | 54793 |
rs553382211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25449748 | GCCACACTGGCTAAT[C/T]GTTACCATATTGAAT | 54793 |
rs553642838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25430547 | CAACACCCCCAGATG[C/G]GACTGTCTAGTTGCA | 54793 |
rs553813781 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25441624 | TTAAAGACTAAAGCA[A/G]AAGAAATACAAGAGT | 54793 |
rs553850272 | snp | C/T | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25454085 | AGAGATGGGATCTCA[C/T]TATGTTGCCCAGGCT | 54793 |
rs553852298 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25459417 | CGACGCTCGCCTGCC[A/G]CGGGGCTCTGGGAGT | 54793 |
rs553854016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25446482 | ACCAAAACAATCTAC[A/T]ATCCTAAGGTGTGTT | 54793 |
rs554060649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454387 | AGTATACAAAAGGCC[C/T]AGGACTTGCACAGCT | 54793 |
rs554392842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25454735 | ACCACACACCCCATT[A/G]GTAACATACTTTTGG | 54793 |
rs554393391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KCTD9 | GRCh38.p7 | 8:25435950 | CACTGATCAGCCCAT[A/G]TATTGCAAATGTACA | 54793 |
rs554407139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25448275 | ATGCTAAATGAAATA[A/C]GCCAGTCACAAAAGG | 54793 |
rs554424747 | snp | A/G | | | intron-variant | KCTD9 | GRCh38.p7 | 8:25439078 | GACTATCTACCTGAA[A/G]GACCACCTGCCCGTG | 54793 |
rs554506404 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25457406 | AGAACAACTTTCATG[A/G]GTGGGGCAAAAGGCT | 54793 |
rs554518883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25451160 | TACAAATAAAAAGGA[A/G]TTATGTTGCAATACT | 54793 |
rs554526322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25440469 | AGATCACATAGTATA[C/T]TTAAGCAGCATTTGA | 54793 |
rs554624080 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429134 | AAGTGTTGTAGTGAT[A/C]GGTAAGTTATTCCTC | 54793 |
rs554726150 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CDCA2, KCTD9 | GRCh38.p7 | 8:25456966 | TAGTAGCTAAGTACA[C/G]AACAGGTTTAGAAAA | 54793 |
rs554769524 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25428708 | ACAGGTGCTGACTGA[C/T]TGATAATTACATCTT | 54793 |
rs555030091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KCTD9 | GRCh38.p7 | 8:25444655 | AGGATAGATTAAAGT[C/T]ACAGCCAACTATTCT | 54793 |
rs555113551 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KCTD9 | GRCh38.p7 | 8:25429625 | CAAAAGGCAGCAATA[G/T]CTAGTTTCCCTACAT | 54793 |