SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2756 | snp | C/G | 0 | 0 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700663 | TTTATTAAGGACATT[C/G]TGTAATGTTTCCACT | 57626 |
rs2757 | snp | C/T | 0 | 0 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700689 | CCACTTTGTTTTAAA[C/T]AATTACAAACATGTG | 57626 |
rs159918 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101330 | CATCTTGTATTTATA[C/T]ATAAGTACATCGTAG | 57626 |
rs159919 | snp | A/G | 0.0229196 | 0.104744 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071564 | tcaccaagacacatc[A/G]cattgcaggccataa | 57626 |
rs299524 | snp | A/C | 0.363359 | 0.222822 | intron-variant | KLHL1 | GRCh38.p7 | 13:70077056 | aagccaccttggaag[A/C]acatttggaagttcc | 57626 |
rs299525 | snp | A/C | 0.345482 | 0.231048 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078072 | TTCTTTTTATTTTTT[A/C]TTTTTTCTGCATTAG | 57626 |
rs299526 | snp | A/G | 0.153665 | 0.230694 | intron-variant | KLHL1 | GRCh38.p7 | 13:70081228 | cagtagaaagttaat[A/G]AGCCAGTGGTACCAG | 57626 |
rs299527 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70080980 | TGGGAAGAGAAGTCT[A/C]TGAATCAAGCTGGAT | 57626 |
rs299530 | snp | C/T | 0.488726 | 0.0742286 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070603 | tctacctcataagaa[C/T]gttaaagaagttatt | 57626 |
rs299531 | snp | G/T | 0.488846 | 0.0738428 | intron-variant | KLHL1 | GRCh38.p7 | 13:70070758 | AGCTCATGGATAAGC[G/T]AACTAACTGATAATG | 57626 |
rs299532 | snp | G/T | 0.489083 | 0.0730708 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071466 | agaaaatatgtaaaa[G/T]agtggttgaactaaa | 57626 |
rs299533 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:70095400 | ttacatggaatctta[C/T]ttaatgtcattaaga | 57626 |
rs299534 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70098956 | TGGATTACATGCTTT[A/G]TACTTAGTCAATATT | 57626 |
rs299535 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099683 | GAAATACACCATACA[A/G]TAAGCTTTTTGTCCC | 57626 |
rs656920 | snp | C/T | 0.370568 | 0.219005 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075173 | aatccatacatctct[C/T]ccctatgaagagagt | 57626 |
rs659582 | snp | A/T | 0.407674 | 0.194008 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075788 | ACATATATATGTATA[A/T]ATATATGTTGCAGGA | 57626 |
rs662481 | snp | A/G | 0.382666 | 0.211895 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075691 | TATATATACACACAC[A/G]TGTGTATATATGAAA | 57626 |
rs663789 | snp | A/G | 0.362523 | 0.223246 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075982 | actctgaggacaaat[A/G]tcaaagctctaaata | 57626 |
rs683300 | snp | C/T | 0.370365 | 0.219117 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074705 | ACTGAATATGGCTTG[C/T]TGAAAATGCTCTCCA | 57626 |
rs694172 | snp | A/C | 0.361263 | 0.223876 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074985 | AAGCTTTCCCCTGGC[A/C]CCTCCATTATTATAA | 57626 |
rs694227 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075443 | CAAAAAGGTTTTTTT[A/T]AATAAAATTTTGTGG | 57626 |
rs717811 | snp | A/G | 0.465683 | 0.126415 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031124 | gccaaccaaaaaaaa[A/G]cccagatgTTAGCTT | 57626 |
rs717812 | snp | A/G | 0.34303 | 0.232046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031447 | CAGAGGTTAACAGTT[A/G]CTCAAAATTTACATT | 57626 |
rs868116 | snp | C/T | 0.492287 | 0.0616198 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938566 | TTATCCCTCTGGATA[C/T]GGAGGCATATTTTTC | 57626 |
rs872603 | snp | A/T | 0.493568 | 0.0563433 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920260 | ATTGTCAGTTTCCAA[A/T]TTTTGGAAAACAGTA | 57626 |
rs872604 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920479 | GCAAAGTTACTTAAC[A/G]CATATCAGAAAAGGG | 57626 |
rs928022 | snp | A/C | 0.159951 | 0.233219 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094590 | GAAGAGCACAGAATT[A/C]ATCTGTAAACCACCA | 57626 |
rs928023 | snp | A/G | 0.158962 | 0.232835 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094711 | TTTGTGGCAATTTCA[A/G]TGTGGCTTCCTTAGC | 57626 |
rs962827 | snp | A/C | 0.26271 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028314 | TTTGCGGCCCATGGA[A/C]AGCCAAAAATATGAA | 57626 |
rs962828 | snp | C/G | 0.26271 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028358 | CAGTATATATATAGA[C/G]AGAGGTATGTCTTGA | 57626 |
rs962829 | snp | C/T | 0.262985 | 0.249663 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028716 | GCATGGTAGTTTATG[C/T]CTGTAATCCCAGCAG | 57626 |
rs962830 | snp | C/T | 0.262159 | 0.249704 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028773 | CTTGAGCCCAGGAGA[C/T]TGAGACCAACCTTCG | 57626 |
rs962831 | snp | C/T | 0.262435 | 0.249691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028809 | TGGCGAAACTTCATC[C/T]CTACAGAAAATACAA | 57626 |
rs973540 | snp | A/G | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861066 | CATCAGTAAAATAAA[A/G]TATGTTTTTAATAGC | 57626 |
rs975701 | snp | A/C | 0.456214 | 0.141336 | intron-variant | KLHL1 | GRCh38.p7 | 13:69758099 | ctcagattttttgat[A/C]gtttgatggtttgaa | 57626 |
rs978025 | snp | A/G | 0.290201 | 0.246747 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025253 | TTAAATATAATCTAC[A/G]AGTATAATGTGCTGA | 57626 |
rs978026 | snp | C/T | 0.29046 | 0.246704 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025307 | CCAAAACATAGGCTG[C/T]AATTCTCAGTGGTGA | 57626 |
rs978027 | snp | C/T | 0.289942 | 0.246789 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025345 | TAGTTGACTTTGAGG[C/T]GGAATTATTTTATGC | 57626 |
rs978028 | snp | C/T | 0.29046 | 0.246704 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025611 | CTAAGAAAAAGTAAA[C/T]TAGGAGATGCTATCT | 57626 |
rs978029 | snp | A/T | 0.290718 | 0.246662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025692 | TTTTACTATATATAT[A/T]ATATATAGTATACAT | 57626 |
rs978885 | snp | C/T | 0.440471 | 0.161928 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053741 | ACCTCTACATAAAAT[C/T]ACTGAATAAAATGAC | 57626 |
rs978886 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70053980 | ATCCTGAATGTGACA[A/G]GTTTTGTGTGGCCTT | 57626 |
rs980122 | snp | A/C | 0.365853 | 0.221536 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087691 | TGGTTGTTTTTCTCC[A/C]TCATTTTAAATCCCA | 57626 |
rs980123 | snp | A/G | 0.315516 | 0.241263 | intron-variant | KLHL1 | GRCh38.p7 | 13:70087594 | GCATTGGGTTTGGTC[A/G]TTGGATTTGCAATGT | 57626 |
rs981349 | snp | C/T | 0.251578 | 0.249995 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024298 | CTTAATTCAAAGAAA[C/T]CTAGTAGTTTATATT | 57626 |
rs981350 | snp | C/G | 0.256619 | 0.249912 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024319 | AGTTTATATTTTCAT[C/G]ATAACCATAACACTT | 57626 |
rs981351 | snp | A/G | 0.255782 | 0.249933 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024413 | GAAAAAACTCAGGGG[A/G]CTTGCCATGAGTGTT | 57626 |
rs981538 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69760853 | AAATTACAGTGGGAC[A/G]TTCAAAATAAACTAT | 57626 |
rs990612 | snp | C/G | 0.486133 | 0.082104 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718390 | CTTTTGACATAGAGA[C/G]CAGCAATGATCAATA | 57626 |
rs990613 | snp | C/T | 0.116838 | 0.211584 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718594 | CATTTCCCCATGGAT[C/T]ATTATGTATCCTATG | 57626 |
rs990614 | snp | A/T | 0.189245 | 0.244197 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718735 | CAGAAGTCTCTGCAT[A/T]GTATTCCTAGGCCTG | 57626 |
rs990615 | snp | A/C | 0.486133 | 0.082104 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718394 | TGACATAGAGACCAG[A/C]AATGATCAATATTCT | 57626 |
rs993138 | snp | G/T | 0.465368 | 0.126951 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805021 | AAACTTTATTTTTCA[G/T]AGAAATATGAATACA | 57626 |
rs993139 | snp | C/T | 0.465158 | 0.127307 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804984 | TCAATGAAATGCTTA[C/T]ACTATAAAACATTGA | 57626 |
rs993140 | snp | A/G | 0.498547 | 0.0269177 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804869 | ACTATTCCAAAATGC[A/G]TCTCACTATTTCCTG | 57626 |
rs993141 | snp | A/G | 0.405776 | 0.195535 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804846 | ATTTCCTGCTTTTTA[A/G]AAGACAATACATCAA | 57626 |
rs993907 | snp | A/T | 0.31721 | 0.240796 | intron-variant | KLHL1 | GRCh38.p7 | 13:70093909 | ATAAAGTTAATTAAC[A/T]TGTTTGAATAATTAA | 57626 |
rs1019580 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854723 | TTACTAACAATTTTG[C/T]TCCAGTTTCTAGAAC | 57626 |
rs1019581 | snp | C/T | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854915 | TACCTATTTTTGAAA[C/T]GGTGCCAACTGGAAA | 57626 |
rs1025821 | snp | C/T | 0.316968 | 0.240864 | intron-variant | KLHL1 | GRCh38.p7 | 13:70050131 | AAAAAACAAACAGCC[C/T]CTAATTTTATAATAT | 57626 |
rs1030272 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780757 | tataaatgtgtgtgt[A/G]tatatatatatgtat | 57626 |
rs1030274 | snp | C/G | 0.441295 | 0.160954 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779935 | gtgccagtaatactt[C/G]ggaggctgtggccgg | 57626 |
rs1030275 | snp | A/G | 0.334412 | 0.235318 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779879 | aggttgcagtgagcc[A/G]agatcgcaccattgc | 57626 |
rs1030276 | snp | A/G | 0.383053 | 0.211653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779649 | GATAAAGATATAGAC[A/G]TATGTGTTTACAATT | 57626 |
rs1030277 | snp | A/T | 0.381113 | 0.21286 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756242 | CATAAATTATCAATA[A/T]CTGCCACAGAGTTAT | 57626 |
rs1118693 | snp | A/G | 0.173643 | 0.238054 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722946 | atggagcacatttcc[A/G]ttatccatttatcca | 57626 |
rs1118694 | snp | C/T | 0.440195 | 0.162252 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722846 | gctgtttctcttata[C/T]actggtttcatttcc | 57626 |
rs1118695 | snp | C/T | 0.187053 | 0.241946 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722820 | tttcctttgaatata[C/T]accaagtagtgagat | 57626 |
rs1119836 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KLHL1 | GRCh38.p7 | 13:69763144 | gtctgttgtgcaacc[A/G]tggcctttgcagtag | 57626 |
rs1273101 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69787021 | ggaatgttcttccat[A/T]tgtttgtatcctctt | 57626 |
rs1318761 | snp | A/G | 0.395818 | 0.203069 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790192 | GTTGTTATTCATGCA[A/G]TTCCTGACAATGTCA | 57626 |
rs1328604 | snp | C/T | 0.35445 | 0.227135 | intron-variant | KLHL1 | GRCh38.p7 | 13:70103151 | CATCTCTGTGATGAA[C/T]AGGGATGAACTCAGG | 57626 |
rs1328622 | snp | A/C | 0.270351 | 0.24917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083723 | TGTAATTATATACGA[A/C]TTAATATTTACAATA | 57626 |
rs1328623 | snp | C/T | 0.289424 | 0.246872 | intron-variant | KLHL1 | GRCh38.p7 | 13:70092551 | TTTTATATTATTAGA[C/T]ACAAAGTTTAATTAA | 57626 |
rs1330084 | snp | A/G | 0.193966 | 0.243639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718659 | TCTTCAGTCCTTACT[A/G]CATACCATATAATAG | 57626 |
rs1330085 | snp | A/G | 0.45762 | 0.139261 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718668 | CTTACTACATACCAT[A/G]TAATAGTTCTAAGTA | 57626 |
rs1330093 | snp | C/T | 0.441295 | 0.160954 | downstream-variant-500B | KLHL1 | GRCh38.p7 | 13:69700441 | AACAATAATTAAAAT[C/T]ACATTTGGTGTCAGC | 57626 |
rs1345908 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69718230 | AGTATCCCAACTTGT[A/G]TCTGGGAGAAAAGCG | 57626 |
rs1345909 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712783 | TTTTTGGGGGGGGGG[G/T]TTTGTTTGTTTGCTT | 57626 |
rs1348175 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061732 | CCAGGTTCTTGCATT[C/T]TCAAATTCCTTGCTA | 57626 |
rs1348176 | snp | C/T | 0.426507 | 0.177046 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062174 | GCACGCTTGTATTTT[C/T]TGAAACATAACAAAT | 57626 |
rs1360011 | snp | C/T | 0.319136 | 0.24025 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083264 | AAGGCATAATAATGA[C/T]GTAGGAGTAAAATAA | 57626 |
rs1364376 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | KLHL1 | GRCh38.p7 | 13:69767312 | TATAACAAACTTAGG[C/T]TTTTCCTAATGATCC | 57626 |
rs1364377 | snp | A/G | 0.461037 | 0.134028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755494 | ATATTTTAATACCAT[A/G]TGTTTACAAATTGTG | 57626 |
rs1364378 | snp | A/T | 0.0894459 | 0.191631 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854203 | AAAGAAAAGAGGTTT[A/T]TTTGGCTCATAGTTC | 57626 |
rs1364379 | snp | C/T | 0.320096 | 0.239972 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854338 | TCACGCAGCAAGAAA[C/T]GAAGAAAGAGAGAGA | 57626 |
rs1364380 | snp | A/G | 0.469049 | 0.120489 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854536 | CCAAACCACAGCACA[A/G]GCACATAAGAAAGGC | 57626 |
rs1372230 | snp | A/T | 0.273049 | 0.248935 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027358 | CCATAGGAGCGTAAA[A/T]CCCTTTAGAGCCAGT | 57626 |
rs1372231 | snp | G/T | 0.294064 | 0.246086 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027546 | AAAGGGGGAGAAAAC[G/T]ATAACAAAAGTTGAT | 57626 |
rs1372232 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065635 | CAGAAAATTTTAGGG[A/T]ACAAAAGATTTCCCT | 57626 |
rs1372281 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016445 | agggagctagagcag[A/G]cacttacgagcctac | 57626 |
rs1372282 | snp | C/T | 0.499295 | 0.0187567 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014617 | GAGATTTTCATTATA[C/T]ATGCATGGATGATAA | 57626 |
rs1372283 | snp | C/G | 0.393987 | 0.204372 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065725 | GTAAATCTGTCCAAA[C/G]CAGAACATTTGCAGT | 57626 |
rs1372284 | snp | A/G | 0.109814 | 0.206997 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065808 | TTTATGTAAAGGCTT[A/G]GCAGGTGGATTAGCA | 57626 |
rs1372285 | snp | A/C | 0.093417 | 0.194889 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067360 | TATTCTTATTCCATT[A/C]TTATTTTATATTGAT | 57626 |
rs1372286 | snp | C/T | 0.404384 | 0.196635 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067425 | AAGGGGAAAGAATTG[C/T]CAAATGTCACACAGC | 57626 |
rs1372287 | snp | C/G | 0.41275 | 0.189769 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067616 | GGTCTTAGTACAGGG[C/G]CTCAGATGACATATT | 57626 |
rs1411333 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709210 | AACATCACAGATAGA[C/T]GCAGACATACATAGA | 57626 |
rs1424300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759468 | attggtaaaataaaa[C/T]agaaatgtctccaaa | 57626 |
rs1424301 | snp | A/G | 0.357024 | 0.225933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741581 | TCTTTGGATCACCCT[A/G]TGGGAATTGGGGCGT | 57626 |
rs1424302 | snp | A/G | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69741079 | TAACCTTTTTGGGAA[A/G]CCAAAGCACAGAAAA | 57626 |
rs1424304 | snp | C/T | 0.493201 | 0.0579089 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717963 | GTTTACCAATATTGC[C/T]ACTCTGTGAAATGGA | 57626 |
rs1424305 | snp | A/G | 0.193653 | 0.243567 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717805 | AATAAATAGGTTTAT[A/G]CTTTTATACTCACAA | 57626 |
rs1424306 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835490 | GGCCAAACACAAGGC[A/G]GGAGAACAAGGAACC | 57626 |
rs1424307 | snp | A/G | 0.084728 | 0.187577 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838672 | CATTTCACATTTCTT[A/G]GCATTGAAATAGCAT | 57626 |
rs1424308 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69711697 | TCAGATGTTTTTGTA[C/T]GTATGCATTTCTAAA | 57626 |
rs1424309 | snp | A/G | 0.334182 | 0.235401 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847024 | AATTGTCTTCTTTCT[A/G]TAAAAATTATCTAAT | 57626 |
rs1424310 | snp | C/G | 0.33875 | 0.233717 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712749 | aaatttataaatttt[C/G]tttgttttttgtttt | 57626 |
rs1424311 | snp | A/G | 0.143959 | 0.226396 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856404 | TTTCTTGCTACTACT[A/G]TTGCCATGAATAACA | 57626 |
rs1424312 | snp | A/G | 0.438946 | 0.163706 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859818 | ATGTCAGTAGAATGC[A/G]TTTTGCATAGGCAAA | 57626 |
rs1424313 | snp | C/T | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69859881 | GTGATCATTATCACA[C/T]TGTAAGCGTACAAAA | 57626 |
rs1424314 | snp | C/T | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860028 | TACAAATTCACTCAA[C/T]TGTTAGGGATTAGAA | 57626 |
rs1424315 | snp | C/T | 0.172351 | 0.237636 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860425 | CTCTTTTTTAAAAAA[C/T]GAGCAAATTTGTCTG | 57626 |
rs1424316 | snp | G/T | 0.079617 | 0.182947 | intron-variant | KLHL1 | GRCh38.p7 | 13:69817617 | ATTCTCTGGAAAAGA[G/T]AAATAGTCTCCCTAG | 57626 |
rs1424317 | snp | A/C | 0.0737376 | 0.17729 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795431 | TATATTTAGAACATA[A/C]ATGTTAGACAGATAA | 57626 |
rs1424318 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69795259 | AATATACACAGATTG[A/T]TGGGGGAagagagag | 57626 |
rs1441542 | snp | A/T | 0.39979 | 0.200158 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031843 | CCATTCTAGATGGAG[A/T]CAGAACAACCATATT | 57626 |
rs1441543 | snp | A/G | 0.264632 | 0.249571 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027732 | TTGTTTCTCACTCAC[A/G]GGATGCAAGCTGCAT | 57626 |
rs1441544 | snp | A/G | 0.294064 | 0.246086 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027423 | CCTGGAAGAAAGGTA[A/G]GCTGTGTTGGGACTC | 57626 |
rs1441545 | snp | C/T | 0.47885 | 0.100637 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026710 | ACACACACACACACA[C/T]ACACACCCTAAGTTC | 57626 |
rs1441546 | snp | A/C | 0.244898 | 0.249948 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026704 | ACACACACACACACA[A/C]CCTAAGTTCTTAAAT | 57626 |
rs1441547 | snp | A/G | 0.290718 | 0.246662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025819 | TCAGAGGTGGTTTAC[A/G]TATGTAGGGCAATTT | 57626 |
rs1441548 | snp | A/G | 0.339429 | 0.233457 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025716 | CATATTTTAATACAT[A/G]TATATCATATGTATA | 57626 |
rs1441549 | snp | C/G | 0.316726 | 0.240931 | intron-variant | KLHL1 | GRCh38.p7 | 13:70105045 | TCCATCAAATACATA[C/G]AGTGCTAGCTGATTT | 57626 |
rs1441550 | snp | C/T | 0.317451 | 0.240729 | intron-variant | KLHL1 | GRCh38.p7 | 13:70088446 | gtgaccctccatcct[C/T]catctccccaagtgt | 57626 |
rs1441551 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69995509 | TCAGAAATTCAGAAG[A/C]TTCACTGATTATAAG | 57626 |
rs1441552 | snp | C/G | 0.471958 | 0.115042 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046791 | AGTGCTGGAATTAAA[C/G]GCCCTTACACCCGGC | 57626 |
rs1441553 | snp | C/T | 0.472147 | 0.114677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046928 | GTATTTGATCCTCCT[C/T]TCACAGTAACAAACA | 57626 |
rs1441554 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048149 | ACAAGTTACATTTTT[A/G]GCAACTTATCTCAAA | 57626 |
rs1441555 | snp | A/C | 0.119978 | 0.213528 | intron-variant | KLHL1 | GRCh38.p7 | 13:70052814 | CAACAAGTGCAAAGG[A/C]CTGTTGTTGAATACG | 57626 |
rs1441556 | snp | A/C | 0.255224 | 0.249945 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021903 | tgccaaagacatatt[A/C]gataaaggacagttt | 57626 |
rs1441557 | snp | A/G | 0.255503 | 0.249939 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021828 | aacaaaacaaaaacc[A/G]atttcttaaaaatgg | 57626 |
rs1441558 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019075 | TTCTTGGACTCTGAC[A/G]TCAAGTCAGGATATT | 57626 |
rs1441559 | snp | A/G | 0.499609 | 0.0139722 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018988 | AATTTGAAATGTTAC[A/G]TGGACTTACTATAGC | 57626 |
rs1441560 | snp | C/T | 0.410905 | 0.191336 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018987 | ATTTGAAATGTTACA[C/T]GGACTTACTATAGCA | 57626 |
rs1441561 | snp | A/G | 0.499551 | 0.0149693 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018880 | CCTCCTGTCCTTTTG[A/G]CTTCAATAACGTTTC | 57626 |
rs1441562 | snp | C/T | 0.499354 | 0.0179596 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014468 | CTTTTGATCATCTGA[C/T]AAATGCTATTGGAAT | 57626 |
rs1441563 | snp | C/T | 0.211516 | 0.24702 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014299 | GCAGAGATCATTATT[C/T]GCTTTTCTTACTGTG | 57626 |
rs1441564 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999415 | TGGCATCAGCATTCC[C/T]TCTCATTATTATGAT | 57626 |
rs1441565 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005832 | AAGTATTGTCATATA[A/T]TAGTAAAAATAAGAA | 57626 |
rs1441566 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006032 | TTCTTTCCCTCAGCC[A/G]CTGGCAACCACCATT | 57626 |
rs1441567 | snp | C/G | 0.139564 | 0.224285 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006668 | GGAAATTGGTTGAAT[C/G]TTTCTCTCATGGACA | 57626 |
rs1441568 | snp | C/T | 0.139564 | 0.224285 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006673 | TTGGTTGAATGTTTC[C/T]CTCATGGACATGTCG | 57626 |
rs1441569 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006885 | AACTATAAATAATCA[C/T]ACAATGTTTTTAAGT | 57626 |
rs1441570 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008641 | TTCATTTACAACCCA[A/C]AATTATTCTCCTCAC | 57626 |
rs1441571 | snp | C/T | 0.136166 | 0.22258 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008687 | TCTCTCACTCAAATG[C/T]TGAAAACAATTGATC | 57626 |
rs1441572 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008895 | AGCAACCTCAAAAAT[A/G]GATCAATATTATTAT | 57626 |
rs1441573 | snp | A/C | 0.414245 | 0.188477 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065601 | GCAATTACCATTTAA[A/C]ACAAAATTTTAAGGA | 57626 |
rs1441574 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066196 | TTACACTCATGCTTC[A/G]AGTTCTCAAGAGGTG | 57626 |
rs1441575 | snp | A/G | 0.427879 | 0.175668 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066258 | TTAAGCAAGGGTAAA[A/G]TTACTAATTTAGTCT | 57626 |
rs1441576 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066362 | GAATACCTACTATAC[A/G]CTGAGAGCTATGTGA | 57626 |
rs1441577 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036828 | AAAAAAAAGACCATG[A/G]CATTAAAATCAAACC | 57626 |
rs1441578 | snp | A/G | 0.475877 | 0.107142 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032081 | AAGTATCCATAATTT[A/G]CAGACTGGTCACTGA | 57626 |
rs1470181 | snp | A/G | 0.439085 | 0.163545 | intron-variant | KLHL1 | GRCh38.p7 | 13:70049424 | GTTCTTCTCACATGT[A/G]CTACCTGACGTCGAT | 57626 |
rs1536943 | snp | C/T | 0.498369 | 0.0285077 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701153 | AAGCATGAATCTGTT[C/T]CTCTAATTGTTCTCA | 57626 |
rs1537283 | snp | G/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877678 | TCCCTTTTTCTCTGG[G/T]CTATAGCAAAGTAAA | 57626 |
rs1537284 | snp | C/G | 0.084364 | 0.187256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877795 | GTCTTCCTTTCCTGA[C/G]CTCCTTTTGTCTACA | 57626 |
rs1550546 | snp | A/G | 0.480382 | 0.097079 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084272 | AGTTATAAAGTACTT[A/G]GTATATACTAGGCAC | 57626 |
rs1559464 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780716 | atatatatatatata[C/T]atatatatatataca | 57626 |
rs1559465 | snp | C/T | 0.361053 | 0.22398 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740301 | ATAAGCTGGTAAAAA[C/T]TGTTTTAAAACATTT | 57626 |
rs1571876 | snp | C/T | 0.339203 | 0.233544 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931713 | ACTTAACTAAGGATA[C/T]CATTTATTTGAAATA | 57626 |
rs1571877 | snp | A/G | 0.43221 | 0.171171 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942282 | TTAGTTTATTGGTGA[A/G]CTTGGAAGGCAGGTT | 57626 |
rs1583917 | snp | A/C | 0.255224 | 0.249945 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021940 | gaatgaaaagacaag[A/C]cacagactgggataa | 57626 |
rs1593176 | snp | A/T | 0.482757 | 0.0912364 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791764 | ccgtgctttgagtta[A/T]ttttgtatttgtcat | 57626 |
rs1593177 | snp | A/G | 0.386123 | 0.209692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69791497 | gatcacactgtcttt[A/G]gtttttattttaaga | 57626 |
rs1596073 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015394 | cctcataggtgatgg[C/T]ggtcacataagacta | 57626 |
rs1596074 | snp | C/T | 0.412082 | 0.190341 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015375 | CACATAAGACTATAA[C/T]ACATATGTTTACCAT | 57626 |
rs1596076 | snp | C/T | 0.117188 | 0.211804 | intron-variant | KLHL1 | GRCh38.p7 | 13:70043729 | CCTACACATGTAGGC[C/T]ACATGGTATAGTCTG | 57626 |
rs1813382 | snp | A/G | 0.372794 | 0.217765 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084209 | ATTCTCAACAGATTA[A/G]TTTACTGTGTGTGTA | 57626 |
rs1819410 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713585 | TTATCACATAAAGGC[A/G]CATTTGGTTTAATAT | 57626 |
rs1822171 | snp | A/C | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039945 | ACCCTGaaaataaat[A/C]aaaaaaaacatattt | 57626 |
rs1822172 | snp | A/T | 0.457388 | 0.139608 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039811 | tgtactaaaaatttt[A/T]aaaattagctaggca | 57626 |
rs1834123 | snp | A/G | 0.499816 | 0.0095829 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716798 | CATGTATTTGGCACT[A/G]TGCTATACAGAGCTT | 57626 |
rs1834124 | snp | C/G | 0.253544 | 0.249975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69830792 | aaatcaactccaaaa[C/G]aaaccctcaaaatca | 57626 |
rs1837783 | snp | A/C | 0.372391 | 0.217992 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076622 | tgaaagaaaacaaaa[A/C]aaaacaaaacaaaat | 57626 |
rs1888897 | snp | G/T | 0.084728 | 0.187577 | | | GRCh38.p7 | 13:69899032 | CATTTTTTTTTTTTT[G/T]TGTGATTCCTCTACA | 57626 |
rs1888898 | snp | C/T | 0.138886 | 0.22395 | | | GRCh38.p7 | 13:69921136 | ACAGAGTTGCAATTA[C/T]AATAGCATTTTCTTT | 57626 |
rs1888899 | snp | C/T | 0.326035 | 0.238157 | | | GRCh38.p7 | 13:69939106 | TAGGTAGCATTGATA[C/T]AGGGCGTCTATGCCA | 57626 |
rs1888900 | snp | C/T | 0.327945 | 0.239372 | | | GRCh38.p7 | 13:69939130 | TATGCCAGGCACCCA[C/T]GCTATTAAATGCTTT | 57626 |
rs1890045 | snp | C/G | 0.451109 | 0.148509 | | | GRCh38.p7 | 13:69790324 | AAACCTCACTGTTCT[C/G]TAGATTTCATTGTTT | 57626 |
rs1890046 | snp | A/G | 0.127599 | 0.217986 | | | GRCh38.p7 | 13:69790168 | AATGTCACTATAAGA[A/G]GTTGCTTTTATATGG | 57626 |
rs1895569 | snp | C/T | 0.455977 | 0.141681 | | | GRCh38.p7 | 13:69743425 | CTCCCAGAATATATG[C/T]GAGTATATTTCAAAT | 57626 |
rs1895570 | snp | G/T | 0.147991 | 0.228242 | | | GRCh38.p7 | 13:69838356 | TTGTGTACTTATTCA[G/T]GAAAATTAAGACAGA | 57626 |
rs1895571 | snp | A/G | 0.0926964 | 0.194308 | | | GRCh38.p7 | 13:69842884 | AATCATGCCATTTAT[A/G]GCAACATGTATGGAA | 57626 |
rs1899311 | snp | A/G | 0.5 | 0 | | | GRCh38.p7 | 13:70038716 | CTGCCTCAGCCTCTA[A/G]AGTAGCTGGGATTAC | 57626 |
rs1899312 | snp | G/T | | | | | GRCh38.p7 | 13:70038937 | catatccaattatgg[G/T]ctgaatttctatttc | 57626 |
rs1899326 | snp | G/T | 0.409552 | 0.192466 | | | GRCh38.p7 | 13:70016482 | ccaaaatcatagttg[G/T]caccaggagcaggga | 57626 |
rs1899327 | snp | A/G | 0.411746 | 0.190626 | | | GRCh38.p7 | 13:70016056 | TGTGTTTGAGTTCTG[A/G]AATTGATATTTTCAT | 57626 |
rs1899328 | snp | G/T | 0.140919 | 0.224948 | | | GRCh38.p7 | 13:70003007 | TTGTAGATATGCAAA[G/T]AAATAATACCTAGAT | 57626 |
rs1899329 | snp | G/T | 0.139903 | 0.224452 | | | GRCh38.p7 | 13:70007675 | TTTGTTGGTGAACCA[G/T]TATATAGAAAATAAT | 57626 |
rs1899330 | snp | A/G | 0.284471 | 0.247612 | | | GRCh38.p7 | 13:70010107 | tagagtggaagaaca[A/G]aagagagtgcaatag | 57626 |
rs1972908 | snp | A/G | 0.498908 | 0.0233371 | intron-variant | KLHL1 | GRCh38.p7 | 13:70084464 | TCAAAAAAAAAAAAA[A/G]AAGAAGAAGAAATAG | 57626 |
rs1974907 | snp | C/T | 0.457504 | 0.139435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740153 | GGAATATTTATATCA[C/T]TTTTGAATAAATAGT | 57626 |
rs1991071 | snp | C/T | 0.193653 | 0.243567 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717270 | GACTGTAAAAATGTT[C/T]TGTAGTATATAATCA | 57626 |
rs1991072 | snp | C/T | 0.444267 | 0.157354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717222 | AAATAGCAAGAATAG[C/T]GTGCAATGCTATGTT | 57626 |
rs1991073 | snp | G/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846683 | CATTAAATTTGTTAC[G/T]ATAATACACCATAAT | 57626 |
rs1991074 | snp | A/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846695 | TACTATAATACACCA[A/T]AATTTACTTGTTGAT | 57626 |
rs1991075 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846818 | CAAATTGCAGCTTTC[C/T]AAGAGTATTATATGA | 57626 |
rs1991076 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852461 | TGATTTCAATAATGA[C/T]GTGGACCTAGTGTTA | 57626 |
rs1991077 | snp | A/G | 0.089084 | 0.191327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852462 | GATTTCAATAATGAC[A/G]TGGACCTAGTGTTAA | 57626 |
rs1991078 | snp | G/T | 0.350327 | 0.228986 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852518 | TCAATTATCTTTAAC[G/T]AAAACCTTTTAATTT | 57626 |
rs1992423 | snp | A/G | 0.443598 | 0.158176 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082769 | CATAGTGTTCCATGG[A/G]GTATATGTACCACAA | 57626 |
rs1992424 | snp | A/T | 0.35207 | 0.228214 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035584 | AACTTTCATAAAAAG[A/T]TCCATTGGTAAACAA | 57626 |
rs1992425 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035355 | tcccacaaacaattg[A/G]gaacatatgaagttt | 57626 |
rs1997615 | snp | C/T | 0.397452 | 0.201886 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035840 | AAAATACTAGACATA[C/T]CCATTTTGTTAGCAT | 57626 |
rs1997616 | snp | C/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004761 | AATGACATTCAATTT[C/T]ATATAATAAAGTTGT | 57626 |
rs1997617 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004747 | TTATATAATAAAGTT[A/G]TTTGGGTGTAATAAA | 57626 |
rs2011847 | snp | C/T | 0.447938 | 0.152711 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024746 | TTGGAGAGAAGAACT[C/T]GCACAGCACAAATGC | 57626 |
rs2015332 | snp | A/G | 0.384401 | 0.210799 | intron-variant | KLHL1 | GRCh38.p7 | 13:69779975 | ctctactaaaaatac[A/G]aaaattagttgggtg | 57626 |
rs2018205 | snp | C/T | 0.491051 | 0.0662916 | intron-variant | KLHL1 | GRCh38.p7 | 13:69726382 | ATGCCATGAGAAAGC[C/T]TGTCAATCCTGCTGT | 57626 |
rs2026128 | snp | A/G | 0.100588 | 0.200439 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713834 | TCTACCAAATTTTAC[A/G]ATATTCTGGGTCATA | 57626 |
rs2026392 | snp | A/G | 0.490063 | 0.0697833 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907226 | ATTTGACCTTTAGGC[A/G]TATTAAATAAATATA | 57626 |
rs2026393 | snp | A/G | 0.498568 | 0.0267188 | intron-variant | KLHL1 | GRCh38.p7 | 13:69907355 | TGTTTCCAAAATGGC[A/G]AATATCTATTGTAAT | 57626 |
rs2026394 | snp | C/T | 0.0984431 | 0.198823 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867891 | TAGCATTAGGAGATA[C/T]ACCTAATGTTAAATA | 57626 |
rs2026684 | snp | C/T | 0.316 | 0.241131 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096992 | ATTCTGCTCCAAATG[C/T]GGTGTAAAATGAATC | 57626 |
rs2033985 | snp | C/T | 0.4231 | 0.180378 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062898 | ATTTGCCTTTTCAGT[C/T]AATTTTTTTCATGTT | 57626 |
rs2033986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063194 | TTCTCTAAGTAGACT[A/G]TGCTAGGTGAGATGC | 57626 |
rs2033987 | snp | A/C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020838 | AAATAGAAAatacat[A/C/T]caaaaatgaatatat | 57626 |
rs2033988 | snp | C/T | 0.499502 | 0.0157669 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012063 | CTTTCTCATGCTGTT[C/T]TTGTGATAGTGAATA | 57626 |
rs2033989 | snp | A/T | 0.499502 | 0.0157669 | intron-variant | KLHL1 | GRCh38.p7 | 13:70011450 | TCTACGGCAAACAAA[A/T]TATCAATAAGGAAGA | 57626 |
rs2042457 | snp | C/T | 0.457853 | 0.138915 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781016 | TGGTCTGATATATTA[C/T]GCTGGAAGAAACTTA | 57626 |
rs2042458 | snp | A/G | 0.351418 | 0.228505 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781015 | GGTCTGATATATTAT[A/G]CTGGAAGAAACTTAC | 57626 |
rs2042459 | snp | A/C | 0.197496 | 0.244424 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837614 | catacatctctctct[A/C]tatatatatgtgtgt | 57626 |
rs2049889 | snp | A/G | 0.254944 | 0.249951 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021301 | aagacactttaatgc[A/G]tattagtgagtggaa | 57626 |
rs2049890 | snp | C/T | 0.300926 | 0.244758 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021119 | tatcataatggtgga[C/T]acatgtcattataca | 57626 |
rs2049891 | snp | C/T | 0.300926 | 0.244758 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021004 | tagtttcaccaatta[C/T]agtgaatgtatcact | 57626 |
rs2049892 | snp | A/G | 0.301177 | 0.244706 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020953 | taggggaggctatac[A/G]tacacagaagcaggg | 57626 |
rs2049893 | snp | A/G | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70008048 | AAAACCAAATAGTAA[A/G]AGCCAATCATCAAAA | 57626 |
rs2059299 | snp | C/T | 0.455977 | 0.141681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69772681 | AAGATACTTTACACA[C/T]GGTAGATGTAAGAAA | 57626 |
rs2081281 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815038 | atttttggactattt[A/T]atttaatttaattta | 57626 |
rs2081282 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815019 | taatttaatttaatt[A/T]attttttaagagacg | 57626 |
rs2113355 | snp | C/T | 0.365439 | 0.221752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754735 | TAAAAAGAAAAGCCA[C/T]TGTGCAACAGAGAGA | 57626 |
rs2113356 | snp | A/G | 0.184838 | 0.241358 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724204 | tggttcaatctggaa[A/G]ggtgggctactccaa | 57626 |
rs2113357 | snp | A/G | 0.21875 | 0.248039 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724168 | aattggggacttcca[A/G]gtcatacataggctt | 57626 |
rs2113358 | snp | A/C | 0.184838 | 0.241358 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724113 | gcacggtatctcacg[A/C]ctgtaatcccagcac | 57626 |
rs2113359 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834467 | ACACTTGGCTTTTCA[C/T]ATCTTCAAAATATTA | 57626 |
rs2113360 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847194 | TCTTGCTGGATGACC[C/T]ACTTTTATTACATAA | 57626 |
rs2113361 | snp | A/C | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847285 | ATTACAGACAACCTT[A/C]TAAAATATCATTTAA | 57626 |
rs2113362 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847601 | CTAACTCTTCTAAAA[C/T]TATATCCTTGGGCTA | 57626 |
rs2113363 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847750 | GTGCTAAAAATAAAC[G/T]CAGAATTTGAATCTA | 57626 |
rs2113364 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847764 | CTCAGAATTTGAATC[C/T]ATAAAACAAAATTGA | 57626 |
rs2113365 | snp | C/T | 0.434831 | 0.168337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865060 | CAGGCGATCCTCCTG[C/T]CTCAGCCTCCTGAGT | 57626 |
rs2113366 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780702 | ACATATATATATATA[C/T]ATATATATATATATA | 57626 |
rs2119583 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020842 | attcatttttgtatg[G/T]atTTTCTATTTTTTA | 57626 |
rs2119584 | snp | A/G | 0.252421 | 0.249988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023293 | CATACCTCTCTCTAC[A/G]TGTGTGTACCTGAGT | 57626 |
rs2119585 | snp | A/G | 0.253264 | 0.249979 | intron-variant | KLHL1 | GRCh38.p7 | 13:70023498 | ACATCATTTAAGTTC[A/G]TACTCACATTTTTCT | 57626 |
rs2119633 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000661 | TAACATATTTGTCTA[A/C]TAAGAAGTTCTAAAA | 57626 |
rs2119634 | snp | C/T | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002493 | TCTACAGTTTTGTCA[C/T]TGTAGTCCCAGGAGG | 57626 |
rs2119635 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002683 | GACAAAAGCATAAGT[C/T]GTTCAAGAAGTGATC | 57626 |
rs2150958 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867876 | gggaggggggaggga[A/T]agcattaggagatat | 57626 |
rs2150959 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69943094 | tggtgaagttttttt[C/T]ttttttcttttttgc | 57626 |
rs2150960 | snp | C/G | 0.326506 | 0.238006 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943285 | GTTGGATGATAGATG[C/G]CTTTGCTTTCAAATA | 57626 |
rs2152779 | snp | A/C | 0.377488 | 0.215835 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754740 | CAGGATAAAAAGAAA[A/C]GCCATTGTGCAACAG | 57626 |
rs2161755 | snp | C/T | 0.184838 | 0.241358 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724300 | tcctgacgacatgtg[C/T]ccaaggtggtcaggg | 57626 |
rs2161756 | snp | C/T | 0.36606 | 0.221428 | intron-variant | KLHL1 | GRCh38.p7 | 13:69834583 | TGTGAGACTTGTCCA[C/T]TTTGGATATCCATTT | 57626 |
rs2161757 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847340 | TACTATACAGTTCAC[A/G]TCCAGAAATAAGAAA | 57626 |
rs2161758 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847371 | AGACCTACATCATAA[G/T]CTATTCCTTAAGTTA | 57626 |
rs2161759 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848005 | GGGAAACAATGATCA[C/T]ATTCAGTGCTAAATG | 57626 |
rs2161760 | snp | A/C | 0.422787 | 0.180679 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856994 | CATATAAATACAATC[A/C]TGCTGTTTCCCTGAA | 57626 |
rs2165517 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70000475 | ATAATACCGTTAGTA[A/G]GCCTGATTTACTAAA | 57626 |
rs2183908 | snp | C/T | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942974 | ATCTAGAACTGTTCC[C/T]CTGCCATTTTTTCAT | 57626 |
rs2194362 | snp | A/C | 0.471196 | 0.1165 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860296 | AAACAAGTAGAAAAC[A/C]AACAAGTATGAGCAT | 57626 |
rs2197044 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022987 | TTCGATCATGTCTTC[A/C]ATATGCATAACACAT | 57626 |
rs2210442 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966818 | actctctatgtccat[A/G]taatcacagctttta | 57626 |
rs2210443 | snp | A/C | 0.481856 | 0.0935034 | intron-variant | KLHL1 | GRCh38.p7 | 13:69974511 | AATGTTTCAAATGAA[A/C]AAGAAAATGTTGAAT | 57626 |
rs2210444 | snp | C/G | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975945 | TATATTTTAATACAA[C/G]TTCAATAAATAAAAG | 57626 |
rs2210445 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69975959 | ACTTCAATAAATAAA[A/G]GTCGAATAATCTATT | 57626 |
rs2210446 | snp | C/G | 0.480697 | 0.0963277 | intron-variant | KLHL1 | GRCh38.p7 | 13:69914081 | TACCCTCGAACATGG[C/G]ACTCCAACTTCTTCA | 57626 |
rs2210447 | snp | A/G | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925262 | CATTGAGCACAGTTC[A/G]GTGAGCTAATGACCT | 57626 |
rs2210448 | snp | A/T | 0.372995 | 0.217652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926336 | AAATGCCATGACTTT[A/T]AAAAAAATAAACATT | 57626 |
rs2210449 | snp | C/G | 0.373598 | 0.21731 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926416 | AATTACATCAATATA[C/G]CAACAAAGCACCTGA | 57626 |
rs2210450 | snp | C/T | 0.292523 | 0.246357 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928305 | acaatctccacactt[C/T]agcccactcaaaaac | 57626 |
rs2210451 | snp | C/G | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944221 | GTTCTGTGTTAGATG[C/G]AGGCCTATGCGATCA | 57626 |
rs2210452 | snp | A/G | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945586 | ATATAAAGAATTTTC[A/G]AACTAAATTTTTAAA | 57626 |
rs2210453 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947526 | ATAATTTAGACAGAT[G/T]TTTTTTCAGATCATC | 57626 |
rs2210454 | snp | C/T | 0.32627 | 0.238082 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947654 | ATAACCATTGTTTTT[C/T]TCAAAGAGTTTTAAT | 57626 |
rs2218245 | snp | G/T | 0.324382 | 0.238678 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022246 | GGAATAGAATAGAGA[G/T]caaagagggaaaaag | 57626 |
rs2225526 | snp | A/C | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976067 | TGTATTGATTAGGAC[A/C]TTAAGTTAGTAAACC | 57626 |
rs2225527 | snp | A/C | 0.483053 | 0.0904792 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976089 | TAGTAAACCTGAAAT[A/C]TCACAGAAATAGTAA | 57626 |
rs2225528 | snp | A/G | 0.489083 | 0.0730708 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919737 | AAACAAGCTACTCAG[A/G]TATTTGGCTTTCTGT | 57626 |
rs2225529 | snp | C/T | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945790 | ATTCTGCAGTTTTAT[C/T]TCTCCTATGATTCAG | 57626 |
rs2225530 | snp | G/T | 0.472335 | 0.114312 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947731 | TGTTAAAGCCAGAAG[G/T]CACAAATGGAATATT | 57626 |
rs2243802 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012640 | CTAAGGCCAGGCACT[A/G]TGGCTCATGCCTGTA | 57626 |
rs2246140 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039922 | cttggattaTTTGaa[A/C]tttaaaaaaatatgt | 57626 |
rs2246141 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039896 | tctgtgtgcctgggc[C/T]tcccaaactgcttgg | 57626 |
rs2246143 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039860 | gggccaggctggtct[C/T]gaaattctgacctca | 57626 |
rs2247589 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002788 | CTAAGTATAAAAAGC[A/G]AAACTATTAACAAGT | 57626 |
rs2325232 | snp | G/T | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768785 | ATTGAGATTTTTTGA[G/T]TTTATTCTAGATCCT | 57626 |
rs2325233 | snp | A/C/T | 0.406828 | 0.205551 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814193 | cacaggcttaccata[A/C/T]gcagaaaaatgaaac | 57626 |
rs2325234 | snp | C/T | 0.396182 | 0.202807 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814316 | TACCTATAAAACACT[C/T]TTCTAGACATTTGCC | 57626 |
rs2325235 | snp | A/G | 0.494815 | 0.0506538 | intron-variant | KLHL1 | GRCh38.p7 | 13:69814840 | acatggtgaaacccc[A/G]tctctactaaaaata | 57626 |
rs2325241 | snp | A/G | 0.329084 | 0.237162 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702852 | GAATATATTCGTGAC[A/G]TATTTGTGTGAAGAA | 57626 |
rs2325242 | snp | G/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69712772 | TTTGTTTTTTTTTTT[G/T]GGGGGGGGGGTTTTG | 57626 |
rs2325243 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945359 | TCAAAGAACAAATGG[A/G]GAAACTAGACTTCAT | 57626 |
rs2325244 | snp | C/T | 0.211819 | 0.247067 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855961 | ttatatatgttataa[C/T]atatataatatacat | 57626 |
rs2325245 | snp | A/G | 0.211516 | 0.24702 | intron-variant | KLHL1 | GRCh38.p7 | 13:69855968 | tgttataacatatat[A/G]atatacatgtttttt | 57626 |
rs2325246 | snp | C/T | 0.419456 | 0.183806 | intron-variant | KLHL1 | GRCh38.p7 | 13:69856887 | CATAGTAATCCTTTT[C/T]CCTCCCCAAGATCAT | 57626 |
rs2325247 | snp | A/C | 0.434398 | 0.168811 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863351 | ATAGAATAGAAAGCT[A/C]TAAATACAAAGGATG | 57626 |
rs2325248 | snp | A/G | 0.433818 | 0.169443 | intron-variant | KLHL1 | GRCh38.p7 | 13:69863474 | TGAATTCTGAATAGA[A/G]TGTATATGAAAAAAA | 57626 |
rs2325249 | snp | G/T | 0.0770498 | 0.180522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896721 | ttgcccaggctggag[G/T]gcagtggtgcaatct | 57626 |
rs2325250 | snp | C/T | 0.178465 | 0.239547 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896937 | agcctcccaatgtgc[C/T]gggattacaggtgtg | 57626 |
rs2325251 | snp | A/G | 0.185788 | 0.241613 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897340 | tcttaaaatttttgg[A/G]caccccaagcactga | 57626 |
rs2325252 | snp | A/G | 0.28052 | 0.24813 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925690 | TAAACTCTAACATTT[A/G]AAGTTTTATTGCCTT | 57626 |
rs2325262 | snp | C/T | 0.255782 | 0.249933 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021554 | tgctgaatctcatgg[C/T]aaacgtatatctagt | 57626 |
rs2325263 | snp | C/T | 0.257732 | 0.24988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022070 | aacccaaagtcactt[C/T]gattttctccttttt | 57626 |
rs2325264 | snp | C/T | 0.262159 | 0.249704 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028797 | ACCTTCGCAATGTGG[C/T]GAAACTTCATCTCTA | 57626 |
rs2325265 | snp | C/T | 0.252421 | 0.249988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028803 | GCAATGTGGCGAAAC[C/T]TCATCTCTACAGAAA | 57626 |
rs2325266 | snp | A/C | 0.333261 | 0.235728 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028891 | ttgaggtgggaggat[A/C]gcttgaacctgggaa | 57626 |
rs2325267 | snp | C/T | 0.262435 | 0.249691 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028948 | CGCCACTGCACTGCA[C/T]TCCAGCTTGGATGAC | 57626 |
rs2325268 | snp | C/T | 0.465788 | 0.126237 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031125 | ccaaccaaaaaaaaa[C/T]ccagatgTTAGCTTT | 57626 |
rs2325269 | snp | A/C | 0.126909 | 0.217598 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032304 | AAAAGCTTGGATAGG[A/C]GAAGTGTTCTTCCTT | 57626 |
rs2325270 | snp | C/T | 0.481319 | 0.0948228 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032431 | GACAGAAAACAATGA[C/T]GGAGCAAATTGAAGA | 57626 |
rs2325271 | snp | A/T | 0.478104 | 0.102316 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032434 | AGAAAACAATGACGG[A/T]GCAAATTGAAGAAAT | 57626 |
rs2325272 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039936 | aatttaaaaaaatat[A/G]tttttttttatttat | 57626 |
rs2325273 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039938 | tttaaaaaaatatgt[A/T]tttttttatttattt | 57626 |
rs2325274 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039952 | tttttttttatttat[C/T]ttCAGGGTTTTCCAG | 57626 |
rs2439605 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022130 | tacaagtagacctgt[C/G]attcattatctatca | 57626 |
rs2439606 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024037 | ATGAGTTTAATTAGT[C/T]GCAAAAAAAATGTAT | 57626 |
rs2439607 | snp | A/G | 0.465683 | 0.126415 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030945 | gaaatagaaactgcc[A/G]tcagagaatactata | 57626 |
rs2439608 | snp | A/C/G | 0.0337553 | 0.125452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035161 | CCATGTTTATTGCAG[A/C/G]ATTATTCACAAGAGC | 57626 |
rs2439610 | snp | C/T | 0.418974 | 0.184249 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037245 | GTTTGTGGTAAAGTC[C/T]CTCAGCTTTTATCTG | 57626 |
rs2439611 | snp | G/T | 0.417521 | 0.185571 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039101 | gggtgttactctatt[G/T]cccaagctggagtac | 57626 |
rs2439612 | snp | C/G | 0.499631 | 0.0135733 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019687 | TATCATTTATAAACT[C/G]TGTAACTTTGGGCAA | 57626 |
rs2439613 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | KLHL1 | GRCh38.p7 | 13:70055256 | acagtccagaagagg[C/T]caatatgtcaaatga | 57626 |
rs2439614 | snp | C/T | 0.171057 | 0.237209 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067004 | ATTTATCAAGCACTT[C/T]GTAAGCTCTAGGCAC | 57626 |
rs2439660 | snp | A/G | 0.475877 | 0.107142 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031967 | CAACCTAAATATCAT[A/G]TTCTTTCTTCTCTAC | 57626 |
rs2439661 | snp | A/G | 0.465788 | 0.126237 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030402 | gtttgattgcactgt[A/G]gtctgagagacagtt | 57626 |
rs2439662 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69996142 | accctgtctctacta[A/G]aaatacaaaaattag | 57626 |
rs2439663 | snp | C/T | 0.131723 | 0.220251 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054317 | ACAGATTAAATAAAG[C/T]CATCTCTGttttgga | 57626 |
rs2439664 | snp | A/T | 0.364817 | 0.222075 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020228 | AACCTCAGTTTATGT[A/T]TTGATGCTGTTAGAA | 57626 |
rs2439665 | snp | G/T | 0.369142 | 0.219784 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020079 | CATTTATGAAGGCTG[G/T]GAAGTCCAAGATCAA | 57626 |
rs2439666 | snp | G/T | 0.499631 | 0.0135733 | intron-variant | KLHL1 | GRCh38.p7 | 13:70019568 | GATAATATATGCAAA[G/T]AATTTAGCAGATCGT | 57626 |
rs2439667 | snp | G/T | 0.499502 | 0.0157669 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017440 | ggtaccagcacaagt[G/T]ttggctctttttgag | 57626 |
rs2439668 | snp | A/G | 0.499464 | 0.016365 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017424 | ttggctctttttgag[A/G]ttgcagctggaccag | 57626 |
rs2439669 | snp | A/G | 0.214541 | 0.247473 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017406 | GCAGCTGGACCAGAT[A/G]TATTGTATGCAGCTT | 57626 |
rs2439670 | snp | A/G | 0.330249 | 0.23677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015559 | ggaagagtcatatgt[A/G]tattcaaagtatggt | 57626 |
rs2439672 | snp | A/C | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012985 | AATTGAAAAATTAAA[A/C]GACAAGTGATAAATA | 57626 |
rs2439673 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997511 | CTTTCCTCTGTTTCT[A/G]TGAGTTTTACTGCTA | 57626 |
rs2439674 | snp | A/G | 0.192088 | 0.2432 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997889 | ttccatatcttgact[A/G]ctgaaaataatagtg | 57626 |
rs2439675 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997930 | AGGAGTGCACGTGTC[C/T]CTTCGAGATCCTGAT | 57626 |
rs2439676 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997987 | AAGTGGGATCACTGA[A/G]TTACATGATAGTTCT | 57626 |
rs2439677 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998759 | GGGTTGTCTGGTCAT[A/C]GTCTCAGAAGGCTGC | 57626 |
rs2439678 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998978 | ACACTCTCACCCACA[C/T]TTCTAGAGGTCCTAG | 57626 |
rs2439679 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999613 | CAGGTTGTTTGTAAG[A/C]TGTAGCTAAAGAAGA | 57626 |
rs2439680 | snp | C/T | 0.141258 | 0.225111 | intron-variant | KLHL1 | GRCh38.p7 | 13:70003909 | ATCAAATTTAATATA[C/T]GGACAGTGTTAAGAG | 57626 |
rs2439681 | snp | A/G | 0.184203 | 0.241186 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005006 | TGCAATGTCATAATT[A/G]TAACGTAAGTCCTAG | 57626 |
rs2439682 | snp | C/T | 0.190519 | 0.242821 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009489 | AAAAAGTGGGTTTTA[C/T]GGCAGAAACTCAGGA | 57626 |
rs2439683 | snp | C/T | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009971 | ACATTTTAAGAGTAA[C/T]CAAAGGAAAGGAGTA | 57626 |
rs2439684 | snp | A/C | 0.484209 | 0.0874434 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061288 | ACAGGACTCACAATT[A/C]AAAGCCTTGGGTTTT | 57626 |
rs2439685 | snp | A/C | 0.0700422 | 0.173537 | intron-variant | KLHL1 | GRCh38.p7 | 13:70068419 | TGACACTGATTAATG[A/C]ATTATGATTTTATTA | 57626 |
rs2439686 | snp | A/C | 0.436123 | 0.166908 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034769 | ATAGCTGTTTAAGAA[A/C]TCTAGATATATGTAT | 57626 |
rs2439687 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033877 | ACGCCTGTAATCCCA[C/G]AGGTGGGGGCAGGAA | 57626 |
rs2439688 | snp | A/G | 0.491157 | 0.065903 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033164 | TTTCTTTCAACATAG[A/G]TCAATAAAATGAAAG | 57626 |
rs2472265 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060309 | ttacattcccaacaa[C/G]agtgtacaatggttc | 57626 |
rs2472266 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:70059944 | gaggggcctagtggg[A/T]tgtgattggcttatg | 57626 |
rs2472267 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70056546 | ctatctttgataatg[A/T]tttatgagctaagga | 57626 |
rs2472268 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | KLHL1 | GRCh38.p7 | 13:70054986 | ttaaccccaatttat[A/G]tctctatctcctccc | 57626 |
rs2472269 | snp | C/G | 0.140242 | 0.224618 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051086 | TTTTTGTAGAAATCC[C/G]TGATTTAGACATTTC | 57626 |
rs2472270 | snp | C/T | 0.497776 | 0.0332724 | intron-variant | KLHL1 | GRCh38.p7 | 13:70037290 | TCCAGTGTCATTACA[C/T]TTCAAAAAGTTAATA | 57626 |
rs2472271 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033804 | GGTAAAACCCCGTTT[C/T]TACTACAAATAAAAA | 57626 |
rs2472272 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70033745 | GTAATTCCAGCTGCT[C/T]TAGAGGCTGAGACAT | 57626 |
rs2472273 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033686 | gctgcagtgagtcaa[A/G]atggtgccactgcat | 57626 |
rs2472274 | snp | A/C | 0.110872 | 0.20771 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022281 | acacacacacacaca[A/C]acacacacGtaatca | 57626 |
rs2472275 | snp | C/G | 0.499451 | 0.0165644 | intron-variant | KLHL1 | GRCh38.p7 | 13:70017425 | tttggctctttttga[C/G]gttgcagctggacca | 57626 |
rs2472276 | snp | A/G | 0.214843 | 0.247516 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016671 | ccaagctgtttgtgc[A/G]gaggggcacctgcag | 57626 |
rs2472277 | snp | C/G | 0.499539 | 0.0151687 | intron-variant | KLHL1 | GRCh38.p7 | 13:70016533 | ggcacacctggcagg[C/G]ttgtgacagcaccca | 57626 |
rs2472279 | snp | A/T | 0.499325 | 0.0183582 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015134 | CATATCCCCATCATT[A/T]AGTGGCACATGACCA | 57626 |
rs2472280 | snp | G/T | 0.499396 | 0.0173617 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015096 | ATATGTGTGTGTTTG[G/T]ACATAATCTACTTTC | 57626 |
rs2472281 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012685 | CTGACCTCGTGATCC[A/G]CCCGCCTCAGCCTCC | 57626 |
rs2472282 | snp | A/G | 0.21303 | 0.247251 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010886 | TTTTTTTTTGAGACG[A/G]AGTTTCACTTTTGTT | 57626 |
rs2472283 | snp | C/G | 0.495708 | 0.0461266 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010644 | attggcctcccaagt[C/G]ctgggattataggca | 57626 |
rs2472284 | snp | A/G | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70009514 | CTTATTTTAGTGTTC[A/G]GGGTCCATCTCCTGA | 57626 |
rs2472285 | snp | G/T | 0.419456 | 0.183806 | intron-variant | KLHL1 | GRCh38.p7 | 13:70005972 | gtaaagttttaggaa[G/T]gcaagatgaaaatgg | 57626 |
rs2472286 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004274 | TATTTGAGGTCCTAC[G/T]TTTTTCTAAATTTCT | 57626 |
rs2472287 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002151 | ATTTTATGTATTAAG[G/T]AGTACAGAGGGAGTA | 57626 |
rs2472289 | snp | A/T | 0.433527 | 0.169758 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063722 | TTAAAATGCATTTTT[A/T]AAAAAAATATTAGAA | 57626 |
rs2482551 | snp | G/T | 0.472989 | 0.113031 | intron-variant | KLHL1 | GRCh38.p7 | 13:69953693 | AGTTGTTTAAAAAAT[G/T]CACCATTATACATGT | 57626 |
rs2482552 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957252 | ATGCCAACAAGTAGA[C/T]AGTGATACATAGATT | 57626 |
rs2482553 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | KLHL1 | GRCh38.p7 | 13:69957673 | AAGTACTGATATACA[A/G]TCTGAATTCCAACTA | 57626 |
rs2482554 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961550 | TCTATTGATCAATCA[A/G]TTAATGCATTTTATT | 57626 |
rs2482555 | snp | A/C | 0.475081 | 0.108804 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961765 | ATGCTAACTTTCCCC[A/C]CTAAACTATCGTGAA | 57626 |
rs2482556 | snp | A/G | 0.475081 | 0.108804 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961768 | CTAACTTTCCCCCCT[A/G]AACTATCGTGAATTT | 57626 |
rs2482557 | snp | A/G | 0.475877 | 0.107142 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965011 | CTTTAGTTCTTAGGC[A/G]TTGTTATTTGTTCTC | 57626 |
rs2482558 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965113 | ATTTGGTTTATCTGA[C/T]GGAAAATGGAATTAC | 57626 |
rs2482560 | snp | A/G | 0.475877 | 0.107142 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967827 | gaagcggagattgca[A/G]tgagccaagatcgca | 57626 |
rs2482561 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968070 | aatcaattgttgcaa[C/T]gtatttcactatcat | 57626 |
rs2482563 | snp | G/T | 0.320335 | 0.239902 | intron-variant | KLHL1 | GRCh38.p7 | 13:69928939 | cgatgtattataaaa[G/T]ATATAAATTTGAAAG | 57626 |
rs2482564 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929199 | TGCTTCACAGTTAAT[A/G]ATAAACACATCAAGT | 57626 |
rs2482565 | snp | A/C | 0.284733 | 0.247575 | intron-variant | KLHL1 | GRCh38.p7 | 13:69929257 | TAAACATTGTTAAAA[A/C]GTCAAGCCTTCTGGT | 57626 |
rs2482566 | snp | A/C | 0.315516 | 0.241263 | intron-variant | KLHL1 | GRCh38.p7 | 13:69930027 | AGCTGTTAAGATATC[A/C]GAAAAATTATTTATT | 57626 |
rs2482567 | snp | A/G | 0.311859 | 0.242226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931220 | TGTCTTTAAGAAATG[A/G]TTACTATAATATCTA | 57626 |
rs2482568 | snp | A/C | 0.290977 | 0.246619 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932831 | TGTAACACGAGTACA[A/C]ATTGCCTGTAAAGAA | 57626 |
rs2482569 | snp | G/T | 0.320096 | 0.239972 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932835 | ACACGAGTACAAATT[G/T]CCTGTAAAGAATAGT | 57626 |
rs2482570 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936965 | CCTGCAACTGCCCGT[A/G]gagaataatggctgc | 57626 |
rs2482571 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69941200 | attctccaagataga[C/T]caggaacaagtctca | 57626 |
rs2482572 | snp | A/T | 0.472896 | 0.113214 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942573 | ATTTTTTCCATATCA[A/T]Attttgttttctgaa | 57626 |
rs2482573 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69944642 | gatttcatttcacac[C/T]aaattaatctataga | 57626 |
rs2482574 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945286 | cAGCTATAAAACTTC[C/T]ATAACCAAACTTTGt | 57626 |
rs2482575 | snp | C/T | 0.474182 | 0.110646 | intron-variant | KLHL1 | GRCh38.p7 | 13:69946928 | TGTCATTACTTTCAA[C/T]GGGAAAATTGCAATT | 57626 |
rs2482576 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951849 | ATCCATATTTAAAAT[C/T]AATATTTCTTAGCCC | 57626 |
rs2482577 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952022 | CTCTTGGATAGTGCA[C/G]TTTGAAGCCATCTTA | 57626 |
rs2501196 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028971 | TGGATGACAGAGTGA[A/G]AACTTGTTAAAAAAA | 57626 |
rs2501197 | snp | A/G | 0.473359 | 0.112298 | intron-variant | KLHL1 | GRCh38.p7 | 13:69938269 | ATAGAATACCAGAGC[A/G]TCACATTTTCAAAAT | 57626 |
rs2501198 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029479 | aaagaattttcaacc[A/C]agaatttcatatcca | 57626 |
rs2501199 | snp | C/T | 0.465788 | 0.126237 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030438 | ctcaggattaagaaa[C/T]tcactcaaaaccact | 57626 |
rs2501200 | snp | A/G | 0.475965 | 0.106957 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031631 | TATAAATCTGTGTTG[A/G]GGTAACAGGATCCTG | 57626 |
rs2501201 | snp | A/G | 0.475965 | 0.106957 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031796 | CAGGAAAGTTATTAA[A/G]CAAGGAAATGCAAAA | 57626 |
rs2501202 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033058 | GATATTTATTTAAAT[A/G]TGCACTTCACTACAT | 57626 |
rs2501203 | snp | A/G | 0.4231 | 0.180378 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033391 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 57626 |
rs2501204 | snp | A/C | 0.44333 | 0.158505 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034335 | AAAATAAAAACACAG[A/C]AATTCTCTTCCCTAT | 57626 |
rs2501205 | snp | A/G | 0.497881 | 0.0324789 | intron-variant | KLHL1 | GRCh38.p7 | 13:70035322 | ATATTAAGTGAAATA[A/G]GACAGGCACAGAAAA | 57626 |
rs2501206 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038405 | GAGTATTCAGTTTTT[A/C]CTGATAAATGTCCTG | 57626 |
rs2501207 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70038479 | TTTTTAAGAAACTGC[A/C]AAATTATTTTCCAGA | 57626 |
rs2501208 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039175 | taggcttgaagagat[C/G]ctccaacctcagctc | 57626 |
rs2501210 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939390 | atacacacacacaca[C/T]gcacacacatacaGG | 57626 |
rs2501211 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939679 | cttcctgaatgcaac[A/G]cgtggaggttcctgg | 57626 |
rs2501212 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69940372 | AAGATAAATATAACT[C/T]GGTAAAGGTCACCAA | 57626 |
rs2501213 | snp | G/T | 0.440333 | 0.16209 | intron-variant | KLHL1 | GRCh38.p7 | 13:70060988 | caggcacacaaagac[G/T]aagttcagatgttct | 57626 |
rs2501214 | snp | C/T | 0.476833 | 0.105105 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061114 | aagtgaggatggtta[C/T]CTCCATCCCCACCTC | 57626 |
rs2501215 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069895 | cagatgaggccgggc[A/G]cggtggctcatgcct | 57626 |
rs2501216 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KLHL1 | GRCh38.p7 | 13:69942630 | aaacccacccatata[A/C]ccttcatctggcttc | 57626 |
rs2501217 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945135 | ggattacagtcaccc[A/G]ccaccacgcccagct | 57626 |
rs2501218 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69950669 | ACTTATCACAGATAT[A/G]TTCTTTTGGTCATTA | 57626 |
rs2501219 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952011 | TGTTATTTCCCCTCT[C/T]GGATAGTGCAGTTTG | 57626 |
rs2501220 | snp | C/T | 0.482083 | 0.0929373 | intron-variant | KLHL1 | GRCh38.p7 | 13:69952367 | TTTTTACATTTTTTC[C/T]TGTAAGACTGAATCC | 57626 |
rs2501221 | snp | C/T | 0.498927 | 0.0231381 | intron-variant | KLHL1 | GRCh38.p7 | 13:69959669 | GTAACTTTTTTTTTT[C/T]CCCCCAAAGGCCTGA | 57626 |
rs2501222 | snp | G/T | 0.475081 | 0.108804 | intron-variant | KLHL1 | GRCh38.p7 | 13:69961776 | CCCCCCTAAACTATC[G/T]TGAATTTGAACGCAT | 57626 |
rs2501223 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962197 | GATTCTTGGTTGATT[C/T]TTATATTGTTACAAT | 57626 |
rs2501224 | snp | A/G/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963986 | AGGGTGATTTTTTTT[A/G/T]AACTTGAAATATACA | 57626 |
rs2501225 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967016 | cactcatcaattgat[A/G]aacaattaggttgat | 57626 |
rs2501226 | snp | C/T | 0.47935 | 0.105741 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967115 | tttgtttcctttgga[C/T]agacactcagtagct | 57626 |
rs2501227 | snp | G/T | 0.476052 | 0.106772 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967792 | caggtggctgaggca[G/T]gagaattgcttgaac | 57626 |
rs2501228 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969545 | TATCAACATAAAGTT[A/G]ACCAGCTTAATCTTA | 57626 |
rs2501229 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69932945 | GATAACCATAAAAAA[A/G]GAGTTTTCCATCTAA | 57626 |
rs2501230 | snp | C/T | 0.292008 | 0.246445 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932951 | CATAAAAAAAGAGTT[C/T]TCCATCTAATTCAGG | 57626 |
rs2501231 | snp | C/T | 0.306927 | 0.243432 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933096 | ATTGTCCCTTAAACG[C/T]TCATTATACTCACCC | 57626 |
rs2501232 | snp | A/C/T | 0.0233062 | 0.105555 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997500 | GGAAACCACCGCTTT[A/C/T]CTCTGTTTCTATGAG | 57626 |
rs2501233 | snp | A/C | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998189 | CTCAGTTCCAAAGCA[A/C]GAGAAGCCTCTGCTT | 57626 |
rs2501234 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998384 | AGCACAATTATACTT[C/T]AACTTCCAATAAACA | 57626 |
rs2501235 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998533 | AAATTGTATATCTGA[A/G]AAAGAGTGAACAGGT | 57626 |
rs2501236 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69998675 | AGTAATGGATGACTA[C/T]AGACTTATCGACTTT | 57626 |
rs2501237 | snp | A/G | 0.181978 | 0.240568 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999368 | ATGACTTGTTGAAAG[A/G]TAAAATCATAGATCT | 57626 |
rs2501238 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999547 | CCAAGCCACTGAATC[A/G]ATAGGTAAGTAAGAG | 57626 |
rs2501239 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001304 | AAATTATTTGACTTA[C/T]GAATTCTGCAAACAT | 57626 |
rs2501240 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70001649 | tgaaacattgggata[A/T]ctatctattatctat | 57626 |
rs2501241 | snp | A/T | 0.039522 | 0.134904 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002197 | AGTTAAAATTACCAT[A/T]CATGCAAAGAAGAAG | 57626 |
rs2501242 | snp | G/T | 0.436976 | 0.165952 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002296 | AGGTCTTTAAAGAAT[G/T]ATTAATGTGTTCAAT | 57626 |
rs2501243 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:70002365 | TAGGAAAATAAAATC[A/G]ATTGGATTGGTTGGA | 57626 |
rs2501244 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004232 | CAAAGTTGAGGATGG[G/T]GAAGCTACCAACTAC | 57626 |
rs2501245 | snp | A/T | 0.140581 | 0.224783 | intron-variant | KLHL1 | GRCh38.p7 | 13:70004489 | CAATCTAATTGGAAG[A/T]TACCACAATTACTAG | 57626 |
rs2501247 | snp | C/T | 0.139903 | 0.224452 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006350 | gatccttttattctg[C/T]tattgaatttggttt | 57626 |
rs2501248 | snp | A/G | 0.499515 | 0.0155675 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012359 | ATTGTATTTACCTAT[A/G]TTTTTCACTTTTAAT | 57626 |
rs2501249 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012577 | TACCTATTATTAAAC[A/T]TGTGATTAGATTATT | 57626 |
rs2739860 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075592 | TATATATGTGTGTGT[A/G]TGTATATATATATAT | 57626 |
rs2739861 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075590 | TATATGTGTGTGTGT[A/G]TATATATATATATAT | 57626 |
rs2770210 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70075563 | tatacctgtgtgtgt[A/G]tatgtgtatatatat | 57626 |
rs2770211 | snp | A/G | 0.256897 | 0.249905 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075565 | tacctgtgtgtgtgt[A/G]tgtgtatatatatat | 57626 |
rs2875573 | snp | G/T | 0.462691 | 0.131387 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804308 | ATATAATTTTTTTGT[G/T]GGGGGGGGAAATAGT | 57626 |
rs2875574 | snp | A/T | 0.0955205 | 0.196561 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839214 | CAAAGAGATGAACAT[A/T]ATGTCATTCCTTAAA | 57626 |
rs2875575 | snp | C/G | 0.326035 | 0.238157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939112 | GCATTGATACAGGGC[C/G]TCTATGCCAGGCACC | 57626 |
rs2875576 | snp | A/G | 0.453087 | 0.145793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936546 | GTGAGTGGAGATTAC[A/G]CCTCTGCACTCCAGC | 57626 |
rs2875585 | snp | C/T | 0.255782 | 0.249933 | intron-variant | KLHL1 | GRCh38.p7 | 13:70021558 | gaatctcatggcaaa[C/T]gtatatctagttttg | 57626 |
rs2875586 | snp | C/T | 0.294064 | 0.246086 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027234 | GAATTAATTCTCCTT[C/T]ACAAACATTATATTC | 57626 |
rs2911503 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843354 | AATAAAAAAGTGAAT[C/G]CAAGAGTTTGGAAAC | 57626 |
rs2911504 | snp | A/T | 0.141934 | 0.225437 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844517 | TTCGTCTCTGACAac[A/T]ctaatgacttcatct | 57626 |
rs2911505 | snp | A/C | 0.137187 | 0.223099 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845344 | TAATAGCTACAAATA[A/C]ATTGCAAATTCAATG | 57626 |
rs2911506 | snp | A/G | 0.205417 | 0.245993 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845807 | ACTAAGTGGAGTTAC[A/G]ATGGAATACTCTGTT | 57626 |
rs2911507 | snp | A/T | 0.209997 | 0.246779 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845887 | CTCAGAGATGTCGAT[A/T]TTTGAAAAAAAATAG | 57626 |
rs2911508 | snp | A/G | 0.123105 | 0.215401 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846195 | TAAAAGATACAGAGC[A/G]TAAGACTTTTCCACA | 57626 |
rs2911509 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846457 | TAGAACTTTTGACAA[C/T]GAATTTGTTAGAGCA | 57626 |
rs2911510 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847119 | ATAGATGCTGCTTGA[C/T]ATTGTAAATAACTTT | 57626 |
rs2911511 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847240 | ATTTTATAGTAAAAG[C/T]CAGAAAACATTTACA | 57626 |
rs2911512 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847827 | AATGACAGTTTCATA[G/T]CTTGCCTTTCAAGTT | 57626 |
rs2911513 | snp | C/T | 0.382085 | 0.212258 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848150 | AAACAGAAAGTGCCT[C/T]ATACCTAGAGAGCTT | 57626 |
rs2911514 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848261 | CTTGGCAGTATGAGA[C/T]AGTTTGTTCACCAAA | 57626 |
rs2911515 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849140 | AGTCAGTGCTTATTT[C/T]GTCCAAGGTGCTATA | 57626 |
rs2911516 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849382 | CACTTTCCCCAATAC[C/T]CTGAAGCACGTTATT | 57626 |
rs2911517 | snp | C/T | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849478 | TAAGCCAAGCACATT[C/T]ATGCTCTCTTTCTCT | 57626 |
rs2911518 | snp | C/T | 0.367091 | 0.220884 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849936 | CAAATTCAATGCATA[C/T]GTTAATAATAATTAT | 57626 |
rs2911519 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850549 | GACCCTTCCATTTCA[C/T]TACTTGCTTTCCATT | 57626 |
rs2911520 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852498 | GGTTTTGTTTTAGCC[C/T]TATTTCAATTATCTT | 57626 |
rs2911521 | snp | C/T | 0.126909 | 0.217598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853454 | GTGAGTCGATTAAGC[C/T]TCTTTCCTTTACAAA | 57626 |
rs2911522 | snp | C/G | 0.126909 | 0.217598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853657 | TAAAGTGGTATTCAC[C/G]AGTGAATGTGATAAT | 57626 |
rs2911523 | snp | C/T | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853841 | AAAATGAAGACATTA[C/T]ATCTTCTTCAAAGTA | 57626 |
rs2911524 | snp | C/T | 0.318896 | 0.240319 | intron-variant | KLHL1 | GRCh38.p7 | 13:69854018 | AAATTACTTCCTATC[C/T]CAAGAAAAGATAATC | 57626 |
rs3003202 | snp | C/T | 0.448836 | 0.15154 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997382 | tttggtaactatagg[C/T]acgacgttgcacaga | 57626 |
rs3003203 | snp | A/T | 0.499451 | 0.0165644 | intron-variant | KLHL1 | GRCh38.p7 | 13:70010899 | ctccgtctcaaaaaa[A/T]aaTAATaataataat | 57626 |
rs3012095 | snp | A/T | 0.206096 | 0.246115 | intron-variant | KLHL1 | GRCh38.p7 | 13:69844764 | tttttcttctgggtt[A/T]tttatttatttattt | 57626 |
rs3012096 | snp | C/T | 0.205723 | 0.246048 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845335 | TTTCACCAATAATAG[C/T]TACAAATAAATTGCA | 57626 |
rs3012097 | snp | C/T | 0.211212 | 0.246973 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845468 | ACTATTTATATTATG[C/T]AAAAAATTTAGCAGA | 57626 |
rs3012098 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KLHL1 | GRCh38.p7 | 13:69845793 | CAAGGTAAAACATAA[C/T]TAAGTGGAGTTACGA | 57626 |
rs3012099 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846381 | AAATATATAGGATAA[A/C]CTCACACAATTTTCA | 57626 |
rs3012100 | snp | A/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846525 | ATAAGTATTTTCCCT[A/T]CAGTTACCTGTTTGA | 57626 |
rs3012101 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69848133 | TCAAACTGTACAAGC[A/G]AAAACAGAAAGTGCC | 57626 |
rs3012102 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849392 | AATACCCTGAAGCAC[A/G]TTATTCTACATTTTA | 57626 |
rs3012103 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849456 | GGAACAGATCATGCT[A/G]TATTCTTAAGCCAAG | 57626 |
rs3012104 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849597 | CTATTACTTTCATGA[A/G]GATTTACTTCATCAC | 57626 |
rs3012105 | snp | G/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849857 | TTTATTTTAAATAAT[G/T]TATTCATTACCAAAG | 57626 |
rs3012106 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69850961 | GTGTTTCTAAATAGC[A/G]TTTGAAGGTTATCTT | 57626 |
rs3012107 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851777 | TTACAGTAAGTTTCT[A/G]GATCATCCTTTCTTG | 57626 |
rs3012108 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851967 | ATGAACTGTATTAGC[C/T]AAATGGGGTCTTAAA | 57626 |
rs3012109 | snp | A/G | 0.125874 | 0.217008 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853232 | GGGAGGGACCCAGTG[A/G]GAAGTAGTTAAATAA | 57626 |
rs3012110 | snp | A/G | 0.125874 | 0.217008 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853239 | ACCCAGTGGGAAGTA[A/G]TTAAATAATGGGGGC | 57626 |
rs3012111 | snp | C/G | 0.125874 | 0.217008 | intron-variant | KLHL1 | GRCh38.p7 | 13:69853255 | TTAAATAATGGGGGC[C/G]TTCACCCTCATGCTG | 57626 |
rs3021374 | snp | C/T | 0.142272 | 0.225598 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843496 | GTATTTTGATGGCTC[C/T]TTTAACTAATTAGGG | 57626 |
rs3024251 | in-del | -/TT | 0.469384 | 0.119877 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734499 | TAGTTCTACTTACTC[-/TT]GTCTTTAAATTCAGA | 57626 |
rs3048159 | in-del | -/AGTA | 0.450734 | 0.149016 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780991 | TCCCCAGATTATTTT[-/AGTA]AAGTAAGTAAGTTTC | 57626 |
rs3048161 | in-del | -/AAC | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69790252 | GGCAAAAAAATATTA[-/AAC]AACTCTGGAAACTAA | 57626 |
rs3048164 | snp | C/T | 0.410061 | 0.192043 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736690 | gtgtatatatatata[C/T]atatatatatctcac | 57626 |
rs3048187 | in-del | -/ATGT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69837657 | tgtgtatatatatat[-/ATGT]gtgtgtgtgtgtgta | 57626 |
rs3048189 | in-del | -/ATG | 0.121022 | 0.21416 | intron-variant | KLHL1 | GRCh38.p7 | 13:69846868 | AATAATACATAAATT[-/ATG]ATGCTAAAGGTATTT | 57626 |
rs3072515 | in-del | -/A/AA/AT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012909 | TCTGTATAAAAAAAA[-/A/AA/AT]TAATAATAATAAATA | 57626 |
rs3072516 | in-del | -/AAAG | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014563 | ATTGAAAATGATAAG[-/AAAG]TGCAAAATAAAGTCT | 57626 |
rs3072562 | in-del | -/AAGA | 0.437542 | 0.165312 | intron-variant | KLHL1 | GRCh38.p7 | 13:69860748 | AAATTCTATTTAAGA[-/AAGA]TGAACAATAATAGAT | 57626 |
rs3072567 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901795 | TCTTTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 57626 |
rs3072568 | in-del | -/CT | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69920115 | TATTATTATAATTCT[-/CT]GACTCAAATATAGAT | 57626 |
rs3072570 | in-del | -/AACA | 0.337158 | 0.234315 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925682 | AAATAAACTCTAACA[-/AACA]TTTGAAGTTTTATTG | 57626 |
rs3072584 | in-del | -/CAA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70067662 | caacaacaacaacaa[-/CAA]aaAGGTTCTTGATGT | 57626 |
rs3072589 | in-del | -/TT | 0.427598 | 0.175951 | intron-variant | KLHL1 | GRCh38.p7 | 13:70097888 | TTGATTTCCTTTCTG[-/TT]TTTTTTTTTTCAATT | 57626 |
rs3072681 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70018052 | AAATAGAACTAGCGC[-/AA]AAAAAAAAGTTGAAA | 57626 |
rs3072710 | in-del | -/TGTGTGTG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70026729 | gtgtgtgtgtgtgtg[-/TGTGTGTG]tgtgtgtAagaggga | 57626 |
rs3221445 | microsatellite | (CA)19/22/23/24/25/26/27/28/29/30 | 0.865172 | 0.0624137 | intron-variant | KLHL1 | GRCh38.p7 | 13:70082312 | CCTCCTTGGACCTGT[lengthTooLong]AAGGNCCCATAGTAG | 57626 |
rs3751427 | snp | C/T | 0.199898 | 0.244928 | synonymous-codon, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107466 | GGACGGGGAGGACGA[C/T]GAAGAGGAAGAGGAG | 57626 |
rs3751428 | snp | A/G | 0.404536 | 0.196516 | utr-variant-5-prime, nc-transcript-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107741 | GGCAGCTCACGCAGG[A/G]GTAGGCTGGTCAGCA | 57626 |
rs3751429 | snp | C/T | 0.0225045 | 0.103662 | utr-variant-5-prime, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70107824 | TCTGCACCCCTAGAG[C/T]CAGAAGACGCTAGGT | 57626 |
rs3812853 | snp | A/G | 0.248066 | 0.249993 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109545 | ATTTCTTATTTTATT[A/G]AAGCGTCCAACTTTG | 57626 |
rs3812854 | snp | A/G | 0.316 | 0.241131 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70109280 | GCTCATTAAAGGAAA[A/G]GTTAAAACATTCCAA | 57626 |
rs3812855 | snp | C/T | 0.347032 | 0.230401 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70108791 | AAAGGTTAAAAGACG[C/T]GGTTCATTAAATAAT | 57626 |
rs3812856 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | KLHL1 | GRCh38.p7 | 13:69882598 | TCAAGGATTATGTTA[C/T]AATAAGAACAAAGGA | 57626 |
rs3904254 | snp | G/T | 0.490453 | 0.0684267 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729260 | AACAAATTTAGTGAG[G/T]CTTCTAGTAAGACAG | 57626 |
rs3909551 | snp | A/G | 0.326741 | 0.23793 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728859 | ATTTACTATGGGAAA[A/G]TGGATTCATTCATTC | 57626 |
rs4053597 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031123 | TGCCAACCAAAAAAA[A/G]ACCCAGATGTTAGCT | 57626 |
rs4053609 | in-del | -/T | 0.169435 | 0.236663 | intron-variant | KLHL1 | GRCh38.p7 | 13:69899019 | AATAAAAATTACACA[-/T]TTTTTTTTTTTTTTG | 57626 |
rs4053610 | snp | C/T | 0.124144 | 0.21601 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075774 | acatatatatatata[C/T]atatatatgtatata | 57626 |
rs4053611 | in-del | -/CACA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70082366 | acacacacacacaca[-/CACA]NNNAAGGAACCATAG | 57626 |
rs4053624 | in-del | -/CAG | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69717761 | TTGTCAGTCTATTAG[-/CAG]CATTTTTAAAATAAA | 57626 |
rs4053625 | in-del | -/TTCCTTCC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69779345 | TCCTTCCTTCCTTCC[-/TTCCTTCC]NNNNNNNCtcctctt | 57626 |
rs4254198 | snp | C/T | 0.47802 | 0.102502 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032496 | AAACAAGTATAATAC[C/T]ATACAATGTCTGTAT | 57626 |
rs4265691 | snp | A/G | 0.401215 | 0.199083 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978892 | CAAGTTGTGGTGGGT[A/G]TACTATTAAAGAAAA | 57626 |
rs4280125 | snp | C/T | 0.483708 | 0.088773 | intron-variant | KLHL1 | GRCh38.p7 | 13:69977879 | TGCACATAGAAAATC[C/T]GAAAAAATTGACAGA | 57626 |
rs4304920 | snp | C/T | 0.361684 | 0.223667 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734362 | gaagtgacagccaag[C/T]aaagctttttcttta | 57626 |
rs4306398 | snp | G/T | 0.00835444 | 0.0641245 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734711 | AAGATACAGCAATAC[G/T]AAATAAATGATTTGT | 57626 |
rs4307825 | snp | G/T | 0.477175 | 0.104362 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978981 | CCTGGTTTGGGGGGC[G/T]GGGGGTCATAGTATT | 57626 |
rs4319628 | snp | C/T | 0.320814 | 0.239761 | intron-variant | KLHL1 | GRCh38.p7 | 13:69815240 | atcattctactaaaa[C/T]gacacctgcactcat | 57626 |
rs4344608 | snp | C/T | 0.465368 | 0.126951 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805019 | CATGTATTCATATTT[C/T]TCTGAAAAATAAAGT | 57626 |
rs4353389 | snp | A/G | 0.3744 | 0.216852 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976897 | AAAATTATTCACTGC[A/G]TATTCTTTCCCTCTC | 57626 |
rs4363753 | snp | A/T | 0.421209 | 0.182174 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816997 | AAAAATAAATATAAT[A/T]AAAAAAGCTTTACAA | 57626 |
rs4412872 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69839319 | AACAAATAAAAATGT[A/G]TAAAATGAATGGCTT | 57626 |
rs4448818 | snp | C/G | 0.17654 | 0.238964 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976923 | CTCTCAAGGTATTTA[C/G]TAGTTATTAACAACA | 57626 |
rs4451848 | snp | C/T | 0.399253 | 0.200558 | intron-variant | KLHL1 | GRCh38.p7 | 13:70039882 | ctgacctcaagtgat[C/T]tgtgtgcctgggcct | 57626 |
rs4474577 | snp | A/G | 0.286303 | 0.24735 | intron-variant | KLHL1 | GRCh38.p7 | 13:69945566 | TAAAATATTATATAC[A/G]GAATATATAAAGAAT | 57626 |
rs4519225 | snp | C/T | 0.447421 | 0.153379 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978272 | TTAAGTCAGGATTTG[C/T]AGGCTGCCAAATGGA | 57626 |
rs4531607 | snp | C/T | 0.309401 | 0.24284 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835489 | GGGCCAAACACAAGG[C/T]GGGAGAACAAGGAAC | 57626 |
rs4545685 | snp | G/T | 0.48978 | 0.0707512 | intron-variant | KLHL1 | GRCh38.p7 | 13:69983956 | aactggatattcaca[G/T]gcagaagagtgaaac | 57626 |
rs4555024 | snp | A/G | 0.469148 | 0.120308 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030208 | aaagttagcaaggat[A/G]tccaggaattgaact | 57626 |
rs4555033 | snp | A/G | 0.350327 | 0.228986 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709316 | ATTTTGAAATATGCA[A/G]AGATTTTTAAACATC | 57626 |
rs4559807 | snp | G/T | 0.449979 | 0.150028 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925251 | GCTCCAACACTCATT[G/T]AGCACAGTTCAGTGA | 57626 |
rs4559808 | snp | C/T | 0.485528 | 0.0838238 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978064 | TGCCTTTCACAAGTT[C/T]GCAAATTACAACCCC | 57626 |
rs4612945 | snp | A/G | 0.44755 | 0.153212 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978281 | GATTTGTAGGCTGCC[A/G]AATGGACCAAAACTG | 57626 |
rs4883847 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916676 | agcacaccagcatgg[C/T]acatgtatacgtatg | 57626 |
rs4883851 | snp | A/G | 0.26271 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027747 | CGTGAGTGAGAAACA[A/G]ATGTTTATTGTTTTA | 57626 |
rs4883852 | snp | G/T | 0.26271 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027869 | CACTCCATGCACAGT[G/T]AATTTTTAGAGGCTG | 57626 |
rs4883853 | snp | C/T | 0.495521 | 0.0471118 | intron-variant | KLHL1 | GRCh38.p7 | 13:70045280 | TTAAGCACAAATACA[C/T]CCTTTTTTGCTTTTA | 57626 |
rs4883854 | snp | C/T | 0.319856 | 0.240042 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061413 | TTAAGTGGTTTTTAC[C/T]GCTTTATTGGAGTCA | 57626 |
rs4883857 | snp | A/G | 0.368529 | 0.220116 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083542 | ATTTTAGACTTTGTA[A/G]ATTAACTCTGTGCAA | 57626 |
rs4883858 | snp | G/T | 0.205723 | 0.246048 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104246 | ACTATTATAGGAAAA[G/T]TATTGTTTATGTGGT | 57626 |
rs4883859 | snp | A/G | 0.284995 | 0.247539 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104674 | ATTATTAAATATGAC[A/G]TCATTGTTTGGTGAT | 57626 |
rs4884860 | snp | C/T | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723849 | gtcagaatttttttt[C/T]tttttttttctgaga | 57626 |
rs4884861 | snp | C/T | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849325 | ACAAATTTAGATGAG[C/T]ATGCCAAAAATTCTA | 57626 |
rs4884862 | snp | A/C | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849331 | TTAGATGAGTATGCC[A/C]AAAATTCTACAATAT | 57626 |
rs4884863 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | KLHL1 | GRCh38.p7 | 13:69908444 | TTTCTATATCTCAAA[C/T]TAACATTCAAATAGT | 57626 |
rs4884865 | snp | C/T | 0.499928 | 0.00598999 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916906 | TTTTTTTAGAAGCCA[C/T]ATACACAATATAGTG | 57626 |
rs4884868 | snp | C/T | 0.456095 | 0.141508 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927981 | gattaacaagaatgc[C/T]ggacagaaatataat | 57626 |
rs4884871 | snp | C/T | 0.408871 | 0.193029 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018572 | TGACTTGTTGGATGA[C/T]TGTGCTGTTTAGTGA | 57626 |
rs4884872 | snp | A/G | 0.251578 | 0.249995 | intron-variant | KLHL1 | GRCh38.p7 | 13:70024120 | CACATTCAGGATGGT[A/G]TGGCGTAGACGATTG | 57626 |
rs4884873 | snp | A/G | 0.476918 | 0.104919 | intron-variant | KLHL1 | GRCh38.p7 | 13:70025346 | AGTTGACTTTGAGGT[A/G]GAATTATTTTATGCA | 57626 |
rs4884874 | snp | C/T | 0.26271 | 0.249677 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027848 | ATTTAGAATTGGTTC[C/T]GGAGCCACTCCATGC | 57626 |
rs4884875 | snp | C/T | 0.469148 | 0.120308 | intron-variant | KLHL1 | GRCh38.p7 | 13:70044181 | cccagttcatactgg[C/T]cttttggagtctgtt | 57626 |
rs4884876 | snp | A/G | 0.461813 | 0.132798 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099508 | AGCATCAAATTCTGT[A/G]AAGTAAGTATAATGG | 57626 |
rs4997494 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69939378 | ATATATATATATATA[C/T]ACACACACACACGCA | 57626 |
rs5000345 | snp | A/G | 0.465892 | 0.126058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029147 | TGTGTTTGTGGTTGG[A/G]GGACTGGTAATGCAC | 57626 |
rs5000346 | snp | C/T | 0.465892 | 0.126058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029158 | TTGGGGGACTGGTAA[C/T]GCACATCCAAAACAA | 57626 |
rs5001469 | snp | G/T | 0.45889 | 0.13735 | intron-variant | KLHL1 | GRCh38.p7 | 13:69804309 | TATAATTTTTTTGTG[G/T]GGGGGGGAAATAGTA | 57626 |
rs5017933 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877475 | ACTATATATATATAT[A/T]TTTTTTTCAGTCATT | 57626 |
rs5804443 | in-del | -/G | 0.450985 | 0.148678 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709638 | CAGAATAATAACATT[-/G]GAGTTACATTAAAAA | 57626 |
rs5804444 | in-del | -/CTT | 0.221141 | 0.248329 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709661 | TTAAAAAATAAAGTC[-/CTT]ATTATTTTTGTTTGT | 57626 |
rs5804445 | in-del | -/AA | 0.467845 | 0.122652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743261 | TGTGATTGCTATGAC[-/AA]ATTTATTCTGGATGT | 57626 |
rs5804447 | in-del | -/T | 0.226779 | 0.248919 | intron-variant | KLHL1 | GRCh38.p7 | 13:69780581 | AGGATTGTATTATGC[-/T]GATTTTTTTTCAGTC | 57626 |
rs5804451 | in-del | -/C | 0.122411 | 0.214991 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851083 | TATACTTAGTAGTCA[-/C]CAACTGAAAAACATA | 57626 |
rs5804452 | in-del | -/TAC | 0.257732 | 0.24988 | intron-variant | KLHL1 | GRCh38.p7 | 13:69851104 | AAAAACATACATATA[-/TAC]ATACTTTTATTTTTT | 57626 |
rs5804456 | in-del | -/C | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69943246 | TTTCTTCATTTAATT[-/C]TTTTTATAATTAAAG | 57626 |
rs5804457 | in-del | -/AA | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70012902 | GCAAGATTCTGTATA[-/AA]AAAAAAATAATAATA | 57626 |
rs5804458 | in-del | -/AAGA | 0.331411 | 0.236373 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014560 | GCTATTGAAAATGAT[-/AAGA]AAGTGCAAAATAAAG | 57626 |
rs5804459 | in-del | -/TC | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70024621 | TGAGGAGAAAAGATT[-/TC]TCTCTCTCTCTCTCT | 57626 |
rs5804461 | in-del | -/T | 0.296873 | 0.245566 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027388 | TGAAAGTGAATGTTG[-/T]TTTTTTTCCCTTCAT | 57626 |
rs5804463 | in-del | -/G | 0.336017 | 0.234736 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027534 | ATTTCATACAGCAAA[-/G]GGGGAGAAAACGATA | 57626 |
rs5804464 | in-del | -/A/AA | 0.493154 | 0.0581045 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028979 | GAGTGAGAACTTGTT[-/A/AA]AAAAAAAAAAAAAAA | 57626 |
rs5804465 | in-del | -/A/AA | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028994 | AAAAAAAAAAAAAAA[-/A/AA]TCACTATTCCTGATT | 57626 |
rs5804466 | in-del | -/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70031125 | CCAACCAAAAAAAAA[-/C]CCAGATGTTAGCTTT | 57626 |
rs5804467 | in-del | -/TT | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70036858 | TTTTTTTTTTTTTTT[-/TT]CTGTCTCAGTTTTTA | 57626 |
rs5804468 | in-del | -/T | 0.427423 | 0.176128 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051945 | GGTTTTATAGAAAGC[-/T]TTTTTTTTTTCATTT | 57626 |
rs5804473 | in-del | -/T | 0.0829062 | 0.185956 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096646 | AGCTGTTTTTTTTTT[-/T]AAAGAAATCTTAGCA | 57626 |
rs5804474 | in-del | -/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70097899 | TTGATTTCCTTTCTG[-/T]TTTTTTTTTTTCAAT | 57626 |
rs6562595 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807313 | tggaccaagcccacc[C/T]ttggcctgagcttgg | 57626 |
rs6562596 | snp | G/T | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826666 | aatttatatgttaat[G/T]atcttgattgagcca | 57626 |
rs6562601 | snp | A/G | 0.47709 | 0.104548 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026892 | TAAAAGTTGTTAGAA[A/G]ATTATGCAGTTGGGC | 57626 |
rs6562602 | snp | C/T | 0.47709 | 0.104548 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026907 | GATTATGCAGTTGGG[C/T]TATTTTTCTATGTTT | 57626 |
rs6562605 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030596 | cacatttaaagcagc[A/G]tgtagagggaaattt | 57626 |
rs6562606 | snp | A/G | 0.399432 | 0.200425 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031015 | gggataaattcctgg[A/G]cacatacaccctccc | 57626 |
rs6562608 | snp | C/G | 0.422315 | 0.181128 | intron-variant | KLHL1 | GRCh38.p7 | 13:70065325 | AGAACTTGCCTATAA[C/G]AGATGACAGTGGCAT | 57626 |
rs6650427 | snp | C/T | 0.162253 | 0.234095 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768903 | TTCTTTTTAATGTTT[C/T]GATTTATGATTTTAT | 57626 |
rs7139807 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70006102 | TCATATAAATGATTT[C/T]ATGTAGTATTTGTCC | 57626 |
rs7139929 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743798 | CTCAAAAAAAACACC[A/G]AAAAACAAAACAAAA | 57626 |
rs7139941 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69743823 | ACaaaACAAAAAAAC[A/G]GAAAAAAAAAAAAAA | 57626 |
rs7140109 | snp | A/G | 0.21875 | 0.248039 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847414 | ATTAGCAAAAAAAAA[A/G]AAAAAAAAAAAAACA | 57626 |
rs7316942 | snp | A/G | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847472 | GTACCAAGCGCAGCA[A/G]TCACATCTATACCTT | 57626 |
rs7317095 | snp | A/C | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847465 | AGGAGATGTACCAAG[A/C]GCAGCAATCACATCT | 57626 |
rs7317137 | snp | A/C | 0.0926964 | 0.194308 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847569 | GTTTAAACATATTAT[A/C]GACCAAAGAAAAAGT | 57626 |
rs7317329 | snp | A/C | 0.143959 | 0.226396 | intron-variant | KLHL1 | GRCh38.p7 | 13:70051689 | AAGCAGCTGCAGGAA[A/C]ATTACTAAGACTAGA | 57626 |
rs7317505 | snp | C/T | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838479 | TTTAAACAAATAATT[C/T]ATTTTCTTTTGAAGG | 57626 |
rs7317932 | snp | A/G | 0.0686151 | 0.172278 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714322 | CAAAAAGAAAACAAG[A/G]AAAAGCTAAACAGCT | 57626 |
rs7318210 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714224 | GTATAATGATGAATG[A/G]AAAGTTCTATTTTGA | 57626 |
rs7318244 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945149 | cgccaccacgcccag[C/T]taattttttgtatgt | 57626 |
rs7318344 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69945006 | tttttttttttttca[A/G]atggagtctcacttt | 57626 |
rs7318401 | snp | C/G | 0.485799 | 0.0830599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714313 | TTGACAGAACAAAAA[C/G]AAAACAAGAAAAAGC | 57626 |
rs7318606 | snp | G/T | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:69847487 | ATCACATCTATACCT[G/T]TCATCTGGTCATGGA | 57626 |
rs7318628 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018873 | AGGAAATGAAACGTT[A/G]TTGAAGCCAAAAGGA | 57626 |
rs7318701 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729647 | TGTTTCTGAGTAACA[C/T]AGGAAAAGTACCCAG | 57626 |
rs7318739 | snp | G/T | 0.158632 | 0.232706 | intron-variant | KLHL1 | GRCh38.p7 | 13:69885049 | GGGTTCACGCCATTC[G/T]CCTGCCTCAGCCTCC | 57626 |
rs7318901 | snp | C/T | 0.295599 | 0.245806 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032579 | CATTCTTACTTACGA[C/T]GTTAGTTAAAAATGA | 57626 |
rs7319197 | snp | A/G | 0.312348 | 0.242101 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939750 | CTCTCCTCATACCTC[A/G]CCCTACACATCTCTT | 57626 |
rs7319310 | snp | A/T | 0.495095 | 0.0492773 | intron-variant | KLHL1 | GRCh38.p7 | 13:70032829 | GTCATAATTGAAATT[A/T]TAGATCTTTTTAAGG | 57626 |
rs7319557 | snp | C/T | 0.447421 | 0.153379 | intron-variant | KLHL1 | GRCh38.p7 | 13:69932580 | TATTCCTTCTTGAAA[C/T]TTTGTTAGTTATATT | 57626 |
rs7319572 | snp | A/G | 0.478932 | 0.10045 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973293 | AGAGTCCTTCAATGA[A/G]GGCAATATGTTAACT | 57626 |
rs7319667 | snp | C/T | 0.16911 | 0.236552 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893455 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCA | 57626 |
rs7319679 | snp | A/T | 0.494855 | 0.0504572 | intron-variant | KLHL1 | GRCh38.p7 | 13:70033031 | GAGTCTGTAAATACA[A/T]TTTTTCAAGCTGATA | 57626 |
rs7319892 | snp | C/G | 0.0854556 | 0.188216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69805395 | AGAAGTCTACTTCTT[C/G]GCTCATAACCAAGGA | 57626 |
rs7320487 | snp | C/T | 0.312348 | 0.242101 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939642 | GTATTGCCTGTTAAG[C/T]GTGCATAAAGCCATA | 57626 |
rs7320643 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893944 | CATCTTACACATCAC[G/T]CTCCAAAAGACACAT | 57626 |
rs7320907 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69976689 | GATAAATATCTTAGA[A/G]AGTAACATGGAGAAT | 57626 |
rs7321156 | snp | A/G | 0.412249 | 0.190198 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718216 | TCAGCTAAACATCTC[A/G]CTTTTCTCCCAGATA | 57626 |
rs7321536 | snp | A/T | 0.491316 | 0.0653198 | intron-variant | KLHL1 | GRCh38.p7 | 13:69918482 | TGCAATGAAATTGAA[A/T]TTTGCACATATAAAA | 57626 |
rs7321844 | snp | A/G | 0.105924 | 0.204309 | intron-variant | KLHL1 | GRCh38.p7 | 13:70015716 | aggtaggctagccta[A/G]gctgtgaggtttgat | 57626 |
rs7322696 | snp | C/T | 0.379354 | 0.213933 | intron-variant | KLHL1 | GRCh38.p7 | 13:70073832 | AGCAAACATAAtttt[C/T]ttttttttttgagat | 57626 |
rs7323344 | snp | A/C | 0.483708 | 0.088773 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714839 | GCTCAAGCAATCCAC[A/C]GTTCTCAGCCTCCAA | 57626 |
rs7323485 | snp | C/T | 0.444 | 0.157683 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714801 | ATTTTGCTCTGTTGT[C/T]CAGGATGGTCTTAAA | 57626 |
rs7323506 | snp | A/C | 0.443866 | 0.157848 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714831 | ACCCCTGAGCTCAAG[A/C]AATCCACAGTTCTCA | 57626 |
rs7323633 | snp | A/G | 0.444931 | 0.15653 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714729 | CTCCCAAGTAGCTGA[A/G]GCCCCAGGGATGTGC | 57626 |
rs7323643 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824222 | TGTATAAAATTTCCC[A/G]AAAGTCCAGGTTGTT | 57626 |
rs7323694 | snp | A/C | 0.311369 | 0.242351 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876985 | gaggttgcagtgagc[A/C]aagactgtgccactg | 57626 |
rs7324005 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69723501 | AGGACCAGATGACTT[C/T]ACTGGTACATTCTCA | 57626 |
rs7324212 | snp | A/T | 0.444267 | 0.157354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973659 | AATTACAACTGTTTC[A/T]TCTTGCAAAAGTATC | 57626 |
rs7324913 | snp | C/T | 0.311369 | 0.242351 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876974 | CCTGCGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 57626 |
rs7324914 | snp | G/T | 0.021333 | 0.101051 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824369 | ACAGTTCCCAAAAAG[G/T]AAGATGATATTTTCT | 57626 |
rs7325061 | snp | G/T | 0.444799 | 0.156695 | intron-variant | KLHL1 | GRCh38.p7 | 13:69714927 | TAGAATAATGCTTGT[G/T]TCATTTATTCGTGCA | 57626 |
rs7325263 | snp | A/C/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061978 | tcttctaggcttttg[A/C/G]caatgtacgataaag | 57626 |
rs7325506 | snp | C/T | 0.481856 | 0.0935034 | intron-variant | KLHL1 | GRCh38.p7 | 13:69973491 | TATTATTATAATAGC[C/T]CCACAATTTTTAGTG | 57626 |
rs7325546 | snp | C/G | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924946 | agagctgctcaccct[C/G]ctgcagtcagcatgt | 57626 |
rs7325599 | snp | A/G | 0.313326 | 0.241847 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925061 | caggctggtagtgca[A/G]gctggggacagcctc | 57626 |
rs7326114 | snp | A/G | 0.412082 | 0.190341 | intron-variant | KLHL1 | GRCh38.p7 | 13:70013119 | GGCCAAGTACATCAA[A/G]TTCTGGCACTCTATT | 57626 |
rs7326264 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | KLHL1 | GRCh38.p7 | 13:69782213 | aacaggaacagctcc[A/G]gtctacagctcccag | 57626 |
rs7326358 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69710085 | ATGTTGCAAATATAA[A/G]TATATATATATACTT | 57626 |
rs7327292 | snp | C/T | 0.251578 | 0.249995 | intron-variant | KLHL1 | GRCh38.p7 | 13:69982850 | ATAAAAGTTTTCAta[C/T]gggaaatcctagcca | 57626 |
rs7327798 | snp | A/T | 0.448708 | 0.151707 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933825 | CTTGAGAAAAAAAAA[A/T]CACAAAGTTCTTTGG | 57626 |
rs7328427 | snp | A/T | 0.465788 | 0.126237 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029273 | GAATATATGGGCAGA[A/T]GAAAGAAATTTGAAC | 57626 |
rs7328492 | snp | A/G | 0.492679 | 0.0600586 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913305 | AGGAGGCAGGGAGCT[A/G]TATCCAAAGCCCCTT | 57626 |
rs7328510 | snp | G/T | 0.179425 | 0.239831 | intron-variant | KLHL1 | GRCh38.p7 | 13:69891417 | TCATACAGGAGAAAA[G/T]AAAATTTTGTTATTT | 57626 |
rs7328565 | snp | C/T | 0.490943 | 0.0666801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727612 | AAAACCACTGTATTC[C/T]AGAATGAAGAACCTG | 57626 |
rs7328694 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69756039 | ATTTATTTAGTTTGC[C/T]TCAGTGTATTCCCCT | 57626 |
rs7329257 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047208 | ATTGTAGATATGAAA[C/T]ATAAGAAAACTTATA | 57626 |
rs7329324 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | KLHL1 | GRCh38.p7 | 13:70083417 | tcaagcaatcctccc[A/T]ccttagctgaatagc | 57626 |
rs7330188 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825214 | AATTGAATTGGTCAG[A/G]CTACTGAGAAGCCAG | 57626 |
rs7330997 | snp | C/T | 0.168785 | 0.236441 | intron-variant | KLHL1 | GRCh38.p7 | 13:70075045 | ATGAACTGACAAAAG[C/T]CAGATTAATAGGAAG | 57626 |
rs7331103 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034887 | TCTCTAATGTTTCTA[C/T]GTGTATTTGAAAATA | 57626 |
rs7331253 | snp | A/T | 0.450105 | 0.149859 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740675 | ATAAAATGAAAAAAA[A/T]TTAAAAATTGAATAG | 57626 |
rs7331292 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69828390 | ccctgtaggcactct[C/G]agtacccagagaaac | 57626 |
rs7331630 | snp | A/G | 0.467439 | 0.123371 | intron-variant | KLHL1 | GRCh38.p7 | 13:69740790 | AACTATTACAATCTC[A/G]TAGAAACTACCTACC | 57626 |
rs7331664 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69842851 | aatagaatgctactt[A/G]gccataagaaagaat | 57626 |
rs7331755 | snp | A/G | 0.487871 | 0.076925 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975100 | AACTATTAGCTTTCA[A/G]ATGAATTATGGCTTT | 57626 |
rs7331758 | snp | A/C | 0.482534 | 0.0918038 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975104 | ATTAGCTTTCAAATG[A/C]ATTATGGCTTTAAAA | 57626 |
rs7331958 | snp | A/G | 0.141934 | 0.225437 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843177 | ttgtTCTCaggtgac[A/G]gacacgccaaatacc | 57626 |
rs7331987 | snp | C/T | 0.357451 | 0.225731 | intron-variant | KLHL1 | GRCh38.p7 | 13:70034655 | TATGCAGTGTATCTA[C/T]GTGTTTGTGTAGAGG | 57626 |
rs7332111 | snp | G/T | 0.474903 | 0.109173 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101396 | AGTTCTGGAGTTTTG[G/T]GTACCTGAAAATCCA | 57626 |
rs7332130 | snp | C/T | 0.434253 | 0.168969 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865727 | CAGGGAGTAAGAAAA[C/T]AATAGCTGTTGAGAA | 57626 |
rs7332166 | snp | A/G | 0.437259 | 0.165632 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975299 | CCTAAAATTAGTATG[A/G]CTGTGAATCCCACAG | 57626 |
rs7332190 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975342 | GAATTTTTCCTCCAT[A/G]GTTATCAACCCTAGT | 57626 |
rs7332296 | snp | C/T | 0.233235 | 0.249437 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078795 | ATGGAATTATTTCAC[C/T]AAAATGAAAATAAAT | 57626 |
rs7332307 | snp | C/G | 0.465892 | 0.126058 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029501 | tcatatccagccaaa[C/G]taagcttcatcagtg | 57626 |
rs7332679 | snp | C/G | 0.233235 | 0.249437 | intron-variant | KLHL1 | GRCh38.p7 | 13:70078870 | ACAAAAGCATGAAAA[C/G]TGAATATGTTGAAAT | 57626 |
rs7332783 | snp | C/T | 0.347032 | 0.230401 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896161 | tttgccccactttct[C/T]catctttacacacag | 57626 |
rs7332894 | snp | A/G | 0.398354 | 0.201224 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029671 | atcgtaaagaccatc[A/G]atgctaggaagaaat | 57626 |
rs7332909 | snp | A/G | 0.434398 | 0.168811 | intron-variant | KLHL1 | GRCh38.p7 | 13:69865958 | AACATTAGCATGAAT[A/G]TATATTGCCATGAGG | 57626 |
rs7333556 | snp | A/T | 0.482831 | 0.0910472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69975212 | ATATATAGCCAAGAT[A/T]ACCTTTCTTTAGTTT | 57626 |
rs7334050 | snp | G/T | 0.237014 | 0.249662 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071740 | taacatatagatcaa[G/T]aagaaattttaaggt | 57626 |
rs7334130 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838239 | CATATTCTATTGTTG[C/T]CAATTCCAGCTTTTT | 57626 |
rs7334579 | snp | A/G | 0.110872 | 0.20771 | intron-variant | KLHL1 | GRCh38.p7 | 13:69786550 | cccacagccaatatc[A/G]tactgaatgggcaaa | 57626 |
rs7334741 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70047471 | TTGTCCCATATAGTA[G/T]AAAACTTTAGTGGCC | 57626 |
rs7334775 | snp | A/G | 0.175897 | 0.238765 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922521 | TGCTTAAGATGTTAA[A/G]TTGGAAATAGATTTA | 57626 |
rs7335183 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729345 | TTAAGCCATAAACCA[A/C]TTTCTTGGTTTTTTC | 57626 |
rs7335378 | snp | A/T | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838166 | TGATTGAAATAAGTT[A/T]TTTTTTTGTTCTGAT | 57626 |
rs7335446 | snp | G/T | 0.169435 | 0.236663 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729180 | TTATTCACTTTTTTT[G/T]TGTGTGTTTTCTTTA | 57626 |
rs7335452 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729186 | ACTTTTTTTGTGTGT[A/G]TTTTCTTTATTCACC | 57626 |
rs7335468 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729206 | CTTTATTCACCAAGT[A/G]AGTCTGGCTGTGCTG | 57626 |
rs7335552 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838219 | AAAGATGTTGGATAT[C/T]TGGTCATATTCTATT | 57626 |
rs7335903 | snp | A/G | 0.174932 | 0.238463 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825678 | GTGTTGTAAGAACAA[A/G]TAAATCCATTTAAGA | 57626 |
rs7335970 | snp | C/T | 0.135143 | 0.222054 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716382 | TATCTTGGGCAGTAT[C/T]AGCACATGGCACCTA | 57626 |
rs7336219 | snp | A/C | 0.030665 | 0.119967 | intron-variant | KLHL1 | GRCh38.p7 | 13:69826083 | cacagaaagacaaat[A/C]cagaatgatctcact | 57626 |
rs7336455 | snp | A/G | 0.35445 | 0.227135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893271 | CTCGCTCTGTCGCCC[A/G]GGCCGGACTGCGGAC | 57626 |
rs7336607 | snp | A/G | 0.316243 | 0.241064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69870226 | tagtggaagtttaag[A/G]ggagccagctggtgc | 57626 |
rs7336910 | snp | C/G | 0.277778 | 0.248452 | intron-variant | KLHL1 | GRCh38.p7 | 13:69893250 | TTTTTTTTTTTGAGA[C/G]GGAGTCTCGCTCTGT | 57626 |
rs7337000 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | KLHL1 | GRCh38.p7 | 13:69901723 | TCTGTTGCAGTAATG[A/G]AAAAGTTTAGGAGAT | 57626 |
rs7337005 | snp | A/G | 0.441158 | 0.161117 | intron-variant | KLHL1 | GRCh38.p7 | 13:69931814 | GAACAGAAATTAGAT[A/G]GGAAATTATGTTACC | 57626 |
rs7337151 | snp | A/C | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947823 | CCAGACCTAGATGTA[A/C]AAAGGCAAAAAGCAG | 57626 |
rs7337362 | snp | A/T | 0.444267 | 0.157354 | intron-variant | KLHL1 | GRCh38.p7 | 13:69716433 | ATGTAGAAAGAGTTT[A/T]AATTATAATGTTAAT | 57626 |
rs7337519 | snp | A/G | 0.304937 | 0.243889 | intron-variant | KLHL1 | GRCh38.p7 | 13:69835221 | AAAGAGAAAAAGGAC[A/G]CTTCTGACTGTTGGA | 57626 |
rs7337863 | snp | A/C | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948095 | TTTAGAGATTGTTTT[A/C]AAAAAAAAATGAAAT | 57626 |
rs7338022 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | KLHL1 | GRCh38.p7 | 13:69813854 | tttaactctattcct[A/G]tcaaatttccaatgt | 57626 |
rs7338117 | snp | A/G | 0.31357 | 0.241783 | intron-variant | KLHL1 | GRCh38.p7 | 13:69948311 | GTATATATCTCTTAC[A/G]TCAGTGAAGAAACTT | 57626 |
rs7338569 | snp | A/G | 0.306679 | 0.24349 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926674 | GAATTCAggccgggc[A/G]cggtagctcaagcct | 57626 |
rs7338696 | snp | C/T | 0.145305 | 0.227022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101355 | TCGTAGTATAAACTA[C/T]AGTTTATACTACCTT | 57626 |
rs7338728 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL1 | GRCh38.p7 | 13:69762398 | tgactaagtgctgca[A/G]ggctttaaagcatta | 57626 |
rs7339006 | snp | A/G | 0.148326 | 0.228391 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838475 | AGTTTTTAAACAAAT[A/G]ATTTATTTTCTTTTG | 57626 |
rs7339175 | snp | A/G | 0.148661 | 0.22854 | intron-variant | KLHL1 | GRCh38.p7 | 13:69838538 | TAAATTATAACTTTC[A/G]CCATTCTTATACTTC | 57626 |
rs7339316 | snp | A/T | 0.444666 | 0.15686 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713388 | tgaaaatcacaaaac[A/T]tttcaatatttgact | 57626 |
rs7339358 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713446 | AAATTAACAACATTA[A/G]TTTATTTTTCAAGTT | 57626 |
rs7339380 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799855 | caggacgcacagcag[A/G]aggtgagcggcaccc | 57626 |
rs7350672 | snp | A/G | 0.346368 | 0.23068 | intron-variant | KLHL1 | GRCh38.p7 | 13:70091060 | CCAAGTTTTATTCCC[A/G]TGCTTATGACTCTCA | 57626 |
rs7350674 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70091110 | CTTTGATCCTGAATA[A/G]GAGTATTCTGTTTTC | 57626 |
rs7350675 | snp | C/T | 0.354881 | 0.226936 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090817 | TACAACTTTCGACTG[C/T]AGCTTGTGACAACTT | 57626 |
rs7358861 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69840169 | AATGTGTAAGCCTAC[C/T]TAATATATAAAACTA | 57626 |
rs7358944 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69837977 | AATCTTATTTCTTTA[A/G]GCTTCTGCATTTTCA | 57626 |
rs7489505 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69884719 | AGGTTTTAGTAGCAA[A/G]AATAATTGCACTTCT | 57626 |
rs7489551 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70039611 | tctctgttttgttaa[A/T]actgcctgcctttgg | 57626 |
rs7489808 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094412 | atatatatatatatg[A/C/T]atatatTGGCTCAAT | 57626 |
rs7489876 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70094411 | tatatatatatatat[A/G]aatatatTGGCTCAA | 57626 |
rs7490019 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69815262 | tgcactcatatgttt[A/G]ctgcagcactattcg | 57626 |
rs7490562 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69989513 | atatcattggtagtt[C/T]gatgggaatagcatt | 57626 |
rs7490682 | snp | A/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69702757 | TTTTAATGGATTATT[A/T]GTAAAAGCTAATTTA | 57626 |
rs7491232 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69780705 | atatatatatatgta[C/T]atatatatatgtata | 57626 |
rs7491267 | snp | A/C | 0.302435 | 0.244439 | intron-variant | KLHL1 | GRCh38.p7 | 13:70020805 | tatatatgtatatgc[A/C]tacatacacatacac | 57626 |
rs7491419 | snp | G/T | 0.313082 | 0.241911 | intron-variant | KLHL1 | GRCh38.p7 | 13:69947275 | AAAATCCCAGAGGAT[G/T]CCACATAGTTTGGCT | 57626 |
rs7491555 | snp | G/T | 0.437824 | 0.164991 | intron-variant | KLHL1 | GRCh38.p7 | 13:69978468 | TAACCACAGGTTAAA[G/T]GAAATATTCTGGTCA | 57626 |
rs7491658 | snp | C/T | 0.250168 | 0.25 | intron-variant | KLHL1 | GRCh38.p7 | 13:69999893 | TCCTTTTATGGATAC[C/T]AATATAGTCGGGATG | 57626 |
rs7981986 | snp | G/T | 0.439363 | 0.163222 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867212 | TATTATAAAGTATTT[G/T]AAGTATTTTGAGAAA | 57626 |
rs7983261 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:70048989 | GTCTACATCATTGCT[G/T]TAAGTATACTTTCTC | 57626 |
rs7983424 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018979 | TAATCAAGTGCTATA[A/G]TAAGTCCATGTAACA | 57626 |
rs7983833 | snp | C/T | 0.434253 | 0.168969 | intron-variant | KLHL1 | GRCh38.p7 | 13:69864138 | ATCTATCTCTTACTC[C/T]GGGGACTTTTATAAA | 57626 |
rs7984026 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | KLHL1 | GRCh38.p7 | 13:69951902 | TTACAGAGTGCTGCC[A/G]AGGGAGCATACAGAT | 57626 |
rs7984190 | snp | A/T | 0.264632 | 0.249571 | intron-variant | KLHL1 | GRCh38.p7 | 13:70028116 | TGAAAGGGGTAGGAA[A/T]TAATCCAGAAAGTCC | 57626 |
rs7984430 | snp | G/T | 0.293037 | 0.246268 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902846 | accaacatagcacat[G/T]tatacatatgcaact | 57626 |
rs7984606 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881529 | CAAGCTTATTTTTGG[A/C]TAACTTTACCAGCCA | 57626 |
rs7984775 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881538 | TTTTGGATAACTTTA[C/T]CAGCCAGAAACCCTG | 57626 |
rs7984801 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881619 | ACAAGACTCAGAATC[A/G]GAGAGAACTAGCCAC | 57626 |
rs7984828 | snp | A/C | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086177 | GAAAGAACAACATGG[A/C]GTGTCAGGAAGCCAG | 57626 |
rs7985061 | snp | C/T | 0.408871 | 0.193029 | intron-variant | KLHL1 | GRCh38.p7 | 13:70064587 | ATGTTTTCCATTTTT[C/T]ATTAATATTCACTTA | 57626 |
rs7985089 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KLHL1 | GRCh38.p7 | 13:70027861 | TCTGGAGCCACTCCA[C/T]GCACAGTTAATTTTT | 57626 |
rs7985099 | snp | A/T | 0.465368 | 0.126951 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924306 | gctgatggaacagaa[A/T]gggaacttactgtgc | 57626 |
rs7985103 | snp | C/T | 0.314301 | 0.241589 | intron-variant | KLHL1 | GRCh38.p7 | 13:70094727 | TGTGGCTTCCTTAGC[C/T]GGCCAAGTGTTTCTA | 57626 |
rs7985131 | snp | C/T | 0.148996 | 0.228688 | upstream-variant-2KB, intron-variant | KLHL1, ATXN8OS | GRCh38.p7 | 13:70110429 | GTTAAACTGAAATGA[C/T]TGACAAAGATGATTA | 57626 |
rs7985162 | snp | A/G | 0.442113 | 0.159977 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867389 | CCTCACCCACAATCA[A/G]TATTTGTTTCAGTTA | 57626 |
rs7985324 | snp | A/G | 0.473909 | 0.111197 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867487 | GAAAAATAAACTAGT[A/G]ATAGAATGTCTTTTA | 57626 |
rs7985539 | snp | G/T | 0.168785 | 0.236441 | intron-variant | KLHL1 | GRCh38.p7 | 13:69902924 | aaataaaTAAATAGA[G/T]AATTCAATACCATAG | 57626 |
rs7985990 | snp | A/G | 0.177503 | 0.239258 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897720 | atttgagtcccaaca[A/G]gtttgacccacccat | 57626 |
rs7986044 | snp | C/T | 0.128976 | 0.218754 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785134 | cctgacctcgtgatc[C/T]gcccgccttggcctc | 57626 |
rs7986047 | snp | C/T | 0.0995161 | 0.199636 | intron-variant | KLHL1 | GRCh38.p7 | 13:69881572 | TAACAATGCTGTACA[C/T]AGAGAATTTTGTAGC | 57626 |
rs7986537 | snp | A/G | 0.140242 | 0.224618 | intron-variant | KLHL1 | GRCh38.p7 | 13:69755121 | gattgggtcatgggg[A/G]tggatccctcatggg | 57626 |
rs7986686 | snp | A/C | 0.498109 | 0.0306926 | intron-variant | KLHL1 | GRCh38.p7 | 13:69801206 | GTTAACTGAAGAATG[A/C]CCACTCTACTGAAAA | 57626 |
rs7986882 | snp | A/G | 0.175254 | 0.238565 | intron-variant | KLHL1 | GRCh38.p7 | 13:69936734 | TTGAAGGTTTAAACA[A/G]CCATTGAAAAAACTA | 57626 |
rs7987365 | snp | G/T | 0.0479149 | 0.147179 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785129 | gatctcctgacctcg[G/T]gatccgcccgccttg | 57626 |
rs7987564 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802808 | agacaggagtcttgc[C/T]gatgctcccggctga | 57626 |
rs7987637 | snp | A/G | 0.454423 | 0.143914 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802975 | catttacaactaatc[A/G]atcataaccaattac | 57626 |
rs7987697 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL1 | GRCh38.p7 | 13:69852332 | TCTCCCACATTTTAT[C/T]TCAGAAATGTTAACT | 57626 |
rs7987706 | snp | C/G | 0.493154 | 0.0581045 | intron-variant | KLHL1 | GRCh38.p7 | 13:70074315 | TCCTTTCTGTCGTCT[C/G]TCTGGTCCCTCTATA | 57626 |
rs7987896 | snp | G/T | 0.456214 | 0.141336 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802859 | actcggtgtctgagg[G/T]gttttgtctgtggct | 57626 |
rs7987960 | snp | C/T | 0.459233 | 0.136827 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803033 | actgcttctctcgac[C/T]agccttAAACAGAAG | 57626 |
rs7988036 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | KLHL1 | GRCh38.p7 | 13:69811477 | attgaaggaatatat[A/C]tcaaaataataagag | 57626 |
rs7988088 | snp | G/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69802941 | AAAAGTATTTATAAg[G/T]ctggtctgagtgcca | 57626 |
rs7988210 | snp | C/G | 0.029116 | 0.117091 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781490 | ttcattattttctag[C/G]acctaggattgatac | 57626 |
rs7988385 | snp | C/T | 0.45762 | 0.139261 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781577 | GCTGTTTCATTGCTG[C/T]TCATTCATGCTTGTT | 57626 |
rs7988402 | snp | A/G | 0.476401 | 0.106032 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803079 | GAGAATTCATGATAT[A/G]TATATTATTAAGAGC | 57626 |
rs7988536 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69849181 | AATAACATCATTTTC[A/C]CTCACCACTAATCTA | 57626 |
rs7989195 | snp | A/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69745272 | tttgtgaaggcctgt[A/T]aaaaacctcttcatt | 57626 |
rs7989334 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069181 | ccacaagccccatac[A/G]ctaccatcacatcaa | 57626 |
rs7989992 | snp | A/C | 0.472052 | 0.11486 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748970 | TTATTTTAAATATCT[A/C]TGTTTTGAAAGTATC | 57626 |
rs7990011 | snp | A/T | 0.326976 | 0.237854 | intron-variant | KLHL1 | GRCh38.p7 | 13:70086707 | GATTGCCCTTTTCAA[A/T]CTTTTTTTTTTTTTC | 57626 |
rs7990106 | snp | A/T | 0.127254 | 0.217792 | intron-variant | KLHL1 | GRCh38.p7 | 13:69781851 | TATAATGGCTATAAA[A/T]GGGATATTAACTTTC | 57626 |
rs7990121 | snp | A/C | 0.141596 | 0.225274 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895343 | TCCAGTATCATGACC[A/C]CCACTCTGACTTTGA | 57626 |
rs7990295 | snp | C/T | 0.472147 | 0.114677 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749009 | CCTGGAAAATATTCA[C/T]ACTTTATGCTTCCAC | 57626 |
rs7990312 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:70069206 | catcaatagtggtcc[G/T]gtataataaaaagga | 57626 |
rs7990606 | snp | A/G | 0.121369 | 0.214369 | intron-variant | KLHL1 | GRCh38.p7 | 13:70007671 | AAGCTTTGTTGGTGA[A/G]CCATTATATAGAAAA | 57626 |
rs7990655 | snp | C/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086793 | TAGTATGCTAATATA[C/G]TTTGATATCTTTCTT | 57626 |
rs7990708 | snp | A/C | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69719221 | gtgtgagagagagag[A/C]gagagagagagagaa | 57626 |
rs7991104 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785632 | cgcattcaaaagcta[A/G]cagaaggcaagaaat | 57626 |
rs7991287 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807154 | cccatgcatatctag[A/G]acaatactcactgct | 57626 |
rs7991370 | snp | G/T | 0.488118 | 0.0761554 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785513 | tcaaagcagtgtgtg[G/T]gtagagggaaattta | 57626 |
rs7991505 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712344 | AAATCTAAAATCCAG[C/T]GTGAGTTGATATTTA | 57626 |
rs7991591 | snp | A/G | 0.461703 | 0.132974 | intron-variant | KLHL1 | GRCh38.p7 | 13:69785648 | cagaaggcaagaaat[A/G]actaaaatcagagca | 57626 |
rs7991639 | snp | A/T | 0.35574 | 0.226537 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749052 | TATATTTTTGTAGAT[A/T]GCCACAATATTTCCA | 57626 |
rs7991925 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL1 | GRCh38.p7 | 13:69806932 | gctacaagttgctga[C/T]cagattaagacacaa | 57626 |
rs7991943 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69919740 | CAAGCTACTCAGATA[C/T]TTGGCTTTCTGTTCT | 57626 |
rs7992119 | snp | C/T | 0.455977 | 0.141681 | intron-variant | KLHL1 | GRCh38.p7 | 13:69807061 | taatactgggccgag[C/T]tttgcctttggcctg | 57626 |
rs7992990 | snp | C/T | 0.040671 | 0.13668 | intron-variant | KLHL1 | GRCh38.p7 | 13:69803379 | CATCCACAATATTAA[C/T]CTGGCTCTAGAGCCC | 57626 |
rs7993163 | snp | A/G | 0.142609 | 0.225759 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715771 | ACTCTGCACTCATGC[A/G]GCTGACTCCAGCAAT | 57626 |
rs7993187 | snp | C/T | 0.277867 | 0.248442 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038280 | attctgtggtagcaa[C/T]gtactatggcttttt | 57626 |
rs7993455 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | KLHL1 | GRCh38.p7 | 13:70104670 | GCTCATTATTAAATA[C/T]GACATCATTGTTTGG | 57626 |
rs7993612 | snp | A/G | 0.199254 | 0.244796 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099517 | TTCTGTAAAGTAAGT[A/G]TAATGGATGACTCCT | 57626 |
rs7993620 | snp | C/T | 0.479583 | 0.0989539 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965835 | aaacctgccacaaca[C/T]ttccttgagccaaag | 57626 |
rs7993817 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | KLHL1 | GRCh38.p7 | 13:69877896 | tttataattaataaa[G/T]aatatCTGATTTTCT | 57626 |
rs7994319 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | KLHL1 | GRCh38.p7 | 13:70099607 | GATTTACATTTTTAT[A/G]CAAAGTAAGGATAAT | 57626 |
rs7994964 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966333 | gctcttaagaattac[A/G]ctaattctactcagc | 57626 |
rs7994975 | snp | A/G | 0.479824 | 0.098392 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966360 | cagccagtgctttag[A/G]aatggaactataaag | 57626 |
rs7995348 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965985 | gtcttctccataaca[C/T]aaaagtgcaaagtga | 57626 |
rs7995380 | snp | C/G | 0.211819 | 0.247067 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895591 | ttctggaggtcagaa[C/G]tgcaggcagagtgta | 57626 |
rs7995720 | snp | C/T | 0.148996 | 0.228688 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759581 | gagacaaagtagatc[C/T]tataagtttcattaa | 57626 |
rs7995761 | snp | A/G | 0.255782 | 0.249933 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022448 | AAAACACATCAAAAT[A/G]TTCTGTGGCATGGTC | 57626 |
rs7995799 | snp | C/G | 0.184203 | 0.241186 | intron-variant | KLHL1 | GRCh38.p7 | 13:69895838 | cagcctccatagtag[C/G]tgagactacatgtgt | 57626 |
rs7996658 | snp | A/G | 0.46885 | 0.12085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030111 | agtccttagagacct[A/G]cgaagagacttagac | 57626 |
rs7996810 | snp | C/G | 0.255503 | 0.249939 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022677 | GATTTCTTATGTATG[C/G]AAATCAGTGGGCTAC | 57626 |
rs7996859 | snp | A/T | 0.204189 | 0.245767 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030242 | ctctgcaccaagcgg[A/T]cctaatagacatcta | 57626 |
rs7997093 | snp | A/G | 0.46885 | 0.12085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70030113 | tccttagagacctac[A/G]aagagacttagactc | 57626 |
rs7997178 | snp | C/T | 0.228253 | 0.249052 | intron-variant | KLHL1 | GRCh38.p7 | 13:69703822 | cctaggagcaatagg[C/T]tatatcatacagcct | 57626 |
rs7997372 | snp | G/T | 0.0861826 | 0.188849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720157 | AATGCAACAATGTTA[G/T]TATGATTGAAAATTG | 57626 |
rs7997609 | snp | A/C | 0.351635 | 0.228408 | intron-variant | KLHL1 | GRCh38.p7 | 13:70031811 | ACAAGGAAATGCAAA[A/C]TATAAAACAAATTAA | 57626 |
rs7998045 | snp | C/T | 0.34989 | 0.229177 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038487 | aaactgccaaattat[C/T]ttccagagtggttgt | 57626 |
rs7998093 | snp | C/T | 0.350327 | 0.228986 | intron-variant | KLHL1 | GRCh38.p7 | 13:70038572 | tgccagcatttggga[C/T]tgtcattaatttttt | 57626 |
rs7998143 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL1 | GRCh38.p7 | 13:69913907 | gagattaacatttga[C/G]tcagtggactgggaa | 57626 |
rs7998496 | snp | C/T | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861286 | CTTTCCTTAGCCCTT[C/T]CCTCTTTAAATTCTC | 57626 |
rs7998782 | snp | A/G | 0.411746 | 0.190626 | intron-variant | KLHL1 | GRCh38.p7 | 13:70018071 | AAAAGTTGAAAATTT[A/G]TCTTTAAATCTATGA | 57626 |
rs7999396 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL1 | GRCh38.p7 | 13:70076049 | aataatgttaagatg[C/T]gagttctcccaaact | 57626 |
rs7999424 | snp | A/C | 0.292523 | 0.246357 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026826 | GTTAATGGATAAAAT[A/C]TAGTGAAAAGGGAAA | 57626 |
rs7999428 | snp | C/T | 0.435837 | 0.167226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861170 | ATTTTTAGTCTACCC[C/T]GTCAACTGATAAGTG | 57626 |
rs7999467 | snp | A/G | 0.20511 | 0.245937 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026578 | AACCCATTTGGGTCC[A/G]TTCCCTCATGAGTAA | 57626 |
rs7999541 | snp | A/G | 0.474544 | 0.10991 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746600 | TTACTTGTTTAATCA[A/G]TTTTTTTTCTCATTT | 57626 |
rs7999565 | snp | A/G | 0.474453 | 0.110094 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746626 | CATTTTCTTTCTCCA[A/G]TATTTTTGTTGTTGT | 57626 |
rs7999570 | snp | C/T | 0.482159 | 0.0927485 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966643 | agatttttgcataca[C/T]gtgcaattttgttac | 57626 |
rs7999602 | snp | C/T | 0.435694 | 0.167385 | intron-variant | KLHL1 | GRCh38.p7 | 13:69861229 | AAATTGCTTTTAGAC[C/T]TCTGGTATCCAGATT | 57626 |
rs7999609 | snp | C/T | 0.474723 | 0.109542 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746784 | GAGAGACCACAGTCA[C/T]AATCAAGATTTACTA | 57626 |
rs7999936 | snp | C/T | 0.482459 | 0.0919928 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966828 | tccatataatcacag[C/T]ttttagcaactactt | 57626 |
rs8000050 | snp | C/T | 0.259397 | 0.249823 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100480 | TTTTTACAGATATGA[C/T]AAACTTGTATTCAAA | 57626 |
rs8000091 | snp | A/G | 0.474903 | 0.109173 | intron-variant | KLHL1 | GRCh38.p7 | 13:69746894 | TTCCTTTCTTTCCAG[A/G]GTCTTGATGCATTTG | 57626 |
rs8000910 | snp | A/T | 0.47709 | 0.104548 | intron-variant | KLHL1 | GRCh38.p7 | 13:70026816 | TGAACTGTATGTTAA[A/T]GGATAAAATATAGTG | 57626 |
rs8000924 | snp | C/T | 0.375 | 0.216506 | intron-variant | KLHL1 | GRCh38.p7 | 13:69966671 | tacatgtatagattg[C/T]gtaatggtcaataca | 57626 |
rs8001406 | snp | A/T | 0.435837 | 0.167226 | intron-variant | KLHL1 | GRCh38.p7 | 13:69866596 | CGCGAGTTAGAGTTA[A/T]GTTCATTTTTAATTA | 57626 |
rs8001504 | snp | C/T | 0.151668 | 0.229849 | intron-variant | KLHL1 | GRCh38.p7 | 13:69821247 | AATCATAAATTATTA[C/T]GAGAAAATAAAGATT | 57626 |
rs8001583 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | KLHL1 | GRCh38.p7 | 13:70100584 | acgatccaccaacct[G/T]ggcctcccaaagtgc | 57626 |
rs8001634 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL1 | GRCh38.p7 | 13:69997103 | gcgcatgtctgtagt[C/T]ccagctactctggag | 57626 |
rs8001858 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL1 | GRCh38.p7 | 13:69792542 | aggactcaataatcc[C/T]acacctacatatata | 57626 |
rs8002832 | snp | G/T | 0.437683 | 0.165152 | intron-variant | KLHL1 | GRCh38.p7 | 13:69867123 | TCAGAAGCATTATTT[G/T]ATTAAAATCCAGGTG | 57626 |
rs8002884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL1 | GRCh38.p7 | 13:69734605 | AAAAACAAAACCATA[C/T]AATGACACTGGCAAA | 57626 |
rs9317834 | snp | G/T | 0.206336 | 0.246157 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709865 | GTTGCTTTTTGTTTG[G/T]CAGAAAATTTTTCTA | 57626 |
rs9317835 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709911 | AAGTGAATAATTTAT[A/G]TAGAATACAGTCTGG | 57626 |
rs9317836 | snp | G/T | 0.499902 | 0.00698814 | intron-variant | KLHL1 | GRCh38.p7 | 13:69709975 | TCTGAATTCATATTA[G/T]CCTCATTTAATTATT | 57626 |
rs9317837 | snp | C/T | 0.412416 | 0.190055 | intron-variant | KLHL1 | GRCh38.p7 | 13:69715910 | TAAGATATAAGGATA[C/T]ACTTTTCAATTAGTA | 57626 |
rs9317838 | snp | A/G | 0.4444 | 0.15719 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717567 | ATTATTTATGCCTCT[A/G]TTCACAAACAACATT | 57626 |
rs9317839 | snp | C/T | 0.438526 | 0.164189 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732774 | TCTAAGACACGCCAT[C/T]GGCTTCATTGAGACT | 57626 |
rs9317840 | snp | A/T | 0.472896 | 0.113214 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748412 | AGAAAATTAGGAAAA[A/T]GCAAAAGCGGAATCC | 57626 |
rs9317841 | snp | A/T | 0.472896 | 0.113214 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748425 | AATGCAAAAGCGGAA[A/T]CCCCTGATAAAACCA | 57626 |
rs9317842 | snp | A/T | 0.472989 | 0.113031 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748582 | GAGATTTGGGTGGGG[A/T]CACAGAGCCAGACCA | 57626 |
rs9317843 | snp | A/G | 0.472896 | 0.113214 | intron-variant | KLHL1 | GRCh38.p7 | 13:69748727 | CAGATAACAGTGCTC[A/G]GCAAATGATAAACTT | 57626 |
rs9317844 | snp | A/C | 0.456332 | 0.141164 | intron-variant | KLHL1 | GRCh38.p7 | 13:69766722 | TAGGCTACTGACTGG[A/C]AAATGGATTAGATTC | 57626 |
rs9317845 | snp | A/G | 0.382666 | 0.211895 | intron-variant | KLHL1 | GRCh38.p7 | 13:69768160 | TACCCAAATATCCAT[A/G]GATCAAGCTTTCTTT | 57626 |
rs9317846 | snp | A/C | 0.496483 | 0.0417852 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922087 | GTGCACACGACAGTG[A/C]CTGGCTAAGTTTTAA | 57626 |
rs9317847 | snp | C/T | 0.462253 | 0.132093 | intron-variant | KLHL1 | GRCh38.p7 | 13:69925543 | tatcacatgtgaaca[C/T]tgacactgttgaagg | 57626 |
rs9317849 | snp | C/T | 0.479258 | 0.0997024 | intron-variant | KLHL1 | GRCh38.p7 | 13:69963912 | tcatttatctgaaga[C/T]ttatttagttgcatg | 57626 |
rs9317850 | snp | A/T | 0.479421 | 0.0993283 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965194 | gatactgcagttttt[A/T]aaaaataattgaagg | 57626 |
rs9317851 | snp | G/T | 0.453697 | 0.14494 | intron-variant | KLHL1 | GRCh38.p7 | 13:69965249 | attccatcaaaacca[G/T]ttttccaacagcatg | 57626 |
rs9317853 | snp | G/T | 0.499653 | 0.0131743 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967535 | gattcttgagatggt[G/T]tctactcctggtgaa | 57626 |
rs9317854 | snp | C/T | 0.499741 | 0.0113788 | intron-variant | KLHL1 | GRCh38.p7 | 13:69967596 | aaggatttagaatat[C/T]acacaacctggtggg | 57626 |
rs9317855 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969469 | TTAATTAAATCATTG[C/T]ATGATACAAACAAAC | 57626 |
rs9317856 | snp | A/C | 0.476227 | 0.106402 | intron-variant | KLHL1 | GRCh38.p7 | 13:69972562 | ACCCCTTCTTTCCTC[A/C]TTATGAGCCCTATCT | 57626 |
rs9317857 | snp | G/T | 0.482831 | 0.0910472 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977228 | GAAACAGTCTCCCAG[G/T]TGCTACAGATATGTT | 57626 |
rs9317858 | snp | A/G | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977407 | TGTGCAAAATTAGTC[A/G]ATAAAAGGCAAACAA | 57626 |
rs9317859 | snp | C/G | 0.482609 | 0.0916147 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977579 | TGGGACAAAAGCCAT[C/G]TGAGGAAATAATGGC | 57626 |
rs9317860 | snp | A/G | 0.483126 | 0.0902898 | intron-variant, upstream-variant-2KB | KLHL1 | GRCh38.p7 | 13:69977661 | ATTGGACTTAAACAC[A/G]TTTTAATCGTATAGA | 57626 |
rs9317861 | snp | C/T | 0.493793 | 0.055364 | intron-variant | KLHL1 | GRCh38.p7 | 13:69979527 | ACTTTAACATTTTAG[C/T]AAATTTACATTATGT | 57626 |
rs9317862 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KLHL1 | GRCh38.p7 | 13:69988169 | tgtttctgtccatgt[G/T]ctcgcattacttagc | 57626 |
rs9317864 | snp | C/T | 0.414448 | 0.1883 | intron-variant | KLHL1 | GRCh38.p7 | 13:70012367 | TACCTATATTTTTCA[C/T]TTTTAATTTTATTAA | 57626 |
rs9317865 | snp | A/G | 0.467642 | 0.123012 | intron-variant | KLHL1 | GRCh38.p7 | 13:70029876 | tgtgcagagacacac[A/G]taggctcaaaataaa | 57626 |
rs9317869 | snp | C/T | 0.114387 | 0.210022 | intron-variant | KLHL1 | GRCh38.p7 | 13:70061160 | ACTCACTTAATGTTT[C/T]AATCAAATTTTCTGT | 57626 |
rs9317870 | snp | A/G | 0.409041 | 0.192888 | intron-variant | KLHL1 | GRCh38.p7 | 13:70062923 | CATGTTCAAAGTTAC[A/G]TGAAACTTTCCTCAA | 57626 |
rs9317871 | snp | A/C | 0.401924 | 0.198543 | intron-variant | KLHL1 | GRCh38.p7 | 13:70063291 | TTATTTCAGGGAGCC[A/C]CTCCACAGACTGCAT | 57626 |
rs9317872 | snp | G/T | 0.400682 | 0.199487 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066513 | TGAGCAGAATTCCTC[G/T]TCAGTGCTACATTAA | 57626 |
rs9317873 | snp | C/T | 0.453209 | 0.145623 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066597 | TTCATAGTCCTTCGT[C/T]GGTAATGAGAAACAT | 57626 |
rs9317874 | snp | A/T | 0.315758 | 0.241197 | intron-variant | KLHL1 | GRCh38.p7 | 13:70066840 | AGTGGCCAAATTTTA[A/T]CATAACAGAATGAAA | 57626 |
rs9317877 | snp | G/T | 0.309648 | 0.24278 | intron-variant | KLHL1 | GRCh38.p7 | 13:70090658 | CACAGAAAGAAGATC[G/T]GAAACTTTCTATTTT | 57626 |
rs9317878 | snp | A/G | 0.474903 | 0.109173 | intron-variant | KLHL1 | GRCh38.p7 | 13:70101709 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 57626 |
rs9529624 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL1 | GRCh38.p7 | 13:69706787 | CAAGTCAGAGTGTAT[C/T]GATTCCCTCCATCAT | 57626 |
rs9529625 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720184 | ATTGCTGAAGTTTAC[C/T]TGATACACTCATCTT | 57626 |
rs9529627 | snp | A/G | 0.194902 | 0.243853 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724815 | ataaaaactcaacaa[A/G]cttggataggaagaa | 57626 |
rs9529628 | snp | A/C | 0.105569 | 0.204058 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725073 | aatcctttaaagagg[A/C]tgccagaaaacctgt | 57626 |
rs9529629 | snp | A/G | 0.467946 | 0.122472 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725131 | atctttatgattctg[A/G]tcaaggaacaattct | 57626 |
rs9529630 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729782 | GAAAAAAAATCAAGT[A/G]AAAAATGGAGCCATT | 57626 |
rs9529631 | snp | A/G | 0.490231 | 0.0692021 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730039 | GTCAATTTAAAAGCG[A/G]CAGTAGAAGAAACTA | 57626 |
rs9529632 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | KLHL1 | GRCh38.p7 | 13:69733646 | gagaatgtgatagca[C/T]tagtcatcagaatgg | 57626 |
rs9529633 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736294 | atgaaaaaattctca[A/G]catcactaatgatca | 57626 |
rs9529634 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | KLHL1 | GRCh38.p7 | 13:69736908 | GGAGTAGCCAATATG[A/G]GAaatagaaacagct | 57626 |
rs9529635 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | KLHL1 | GRCh38.p7 | 13:69737220 | gcccataccaccagg[G/T]ccttcagtcacaagc | 57626 |
rs9529636 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69741478 | ATTAAGACATGACTC[C/T]TAGATCAAAGAAGAA | 57626 |
rs9529638 | snp | A/G | 0.030278 | 0.119257 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775746 | ctaggactggagtgc[A/G]gtggtgccatcttag | 57626 |
rs9529644 | snp | A/C/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69810443 | cctgaatgacttttg[A/C/G]ttaaaaaacaaaatt | 57626 |
rs9529645 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69816144 | TAGATTAGAAGATAT[A/G]TAATTTTGATGTTCA | 57626 |
rs9529646 | snp | C/G | 0.352938 | 0.227824 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831483 | gaaaacagaagtcca[C/G]gacccagtggattca | 57626 |
rs9529650 | snp | C/T | 0.186421 | 0.24178 | intron-variant | KLHL1 | GRCh38.p7 | 13:69896041 | agctcattcacattg[C/T]tggtagaatttgctt | 57626 |
rs9529651 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | KLHL1 | GRCh38.p7 | 13:69909366 | GAAATAACCCAAGTG[C/T]AAAATATTTTACATT | 57626 |
rs9529652 | snp | A/C | 0.483345 | 0.0897213 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910049 | GCTATCATCATCTAT[A/C]AAATGAAGCATGTGT | 57626 |
rs9529653 | snp | A/G | 0.481473 | 0.0944461 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910520 | CCACTACTATGTTTC[A/G]GGTATCGGATGGCTG | 57626 |
rs9529654 | snp | C/T | 0.482609 | 0.0916147 | intron-variant | KLHL1 | GRCh38.p7 | 13:69910526 | CTATGTTTCGGGTAT[C/T]GGATGGCTGTGGATA | 57626 |
rs9529655 | snp | C/G | 0.480853 | 0.0959518 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911022 | TTTGAGAGTAAAATA[C/G]TTCAAAGATCAGTAT | 57626 |
rs9529656 | snp | C/T | 0.483995 | 0.0880135 | intron-variant | KLHL1 | GRCh38.p7 | 13:69916303 | cacgtatgtttattg[C/T]ggcactattcacaat | 57626 |
rs9529657 | snp | A/G | 0.497881 | 0.0324789 | intron-variant | KLHL1 | GRCh38.p7 | 13:69922850 | TTCCTTAAGTTGGGT[A/G]GTACTTTCATGGAAA | 57626 |
rs9529660 | snp | A/G | 0.454182 | 0.144256 | intron-variant | KLHL1 | GRCh38.p7 | 13:69962292 | AATTTATTAATTGAG[A/G]AATTCATAGATTCAT | 57626 |
rs9529661 | snp | C/T | 0.480697 | 0.0963277 | intron-variant | KLHL1 | GRCh38.p7 | 13:69968811 | ATTTTCTTAATCGAG[C/T]CTATCATTGTTGGAC | 57626 |
rs9529662 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69969331 | CTGGGCAGTTAGTAA[C/T]TAAAATGTCAACTTT | 57626 |
rs9529663 | snp | C/T | 0.279991 | 0.248195 | intron-variant | KLHL1 | GRCh38.p7 | 13:69985700 | cattttattacagca[C/T]tattaacaatagaca | 57626 |
rs9529664 | snp | C/T | 0.432063 | 0.171327 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986599 | ATTCTGCTGCTTGTT[C/T]TATTCTTATGGAGTG | 57626 |
rs9529665 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:69986649 | TATGAAAATAAGATA[C/T]GCTGATGTTTGGTAA | 57626 |
rs9529666 | snp | A/G | 0.442385 | 0.15965 | intron-variant | KLHL1 | GRCh38.p7 | 13:69989172 | cagtatcacttttct[A/G]catgtagctatctag | 57626 |
rs9529667 | snp | C/T | 0.282632 | 0.247861 | intron-variant | KLHL1 | GRCh38.p7 | 13:69991112 | tgaaagtaatgagaa[C/T]aaaggtacaacatac | 57626 |
rs9529669 | snp | A/G | 0.49934 | 0.0181589 | intron-variant | KLHL1 | GRCh38.p7 | 13:70014950 | TTTAATACATAACAT[A/G]TGGTTTATTAAAAAT | 57626 |
rs9529670 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL1 | GRCh38.p7 | 13:70022347 | TATTCCATTGACCTA[C/G]TTCCTATATGTTTTC | 57626 |
rs9529671 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70046866 | TGCAATCAGGACCCT[C/T]TTCCTCTCTCCAAAG | 57626 |
rs9529672 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046874 | GGACCCTCTTCCTCT[C/T]TCCAAAGCATTAAGG | 57626 |
rs9529673 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:70046977 | TTTAATAAACTTATT[C/T]TGCAAATACTTATCT | 57626 |
rs9529674 | snp | A/C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70047150 | GAACAGGCTTAGGGT[A/C/T]TAAAATGTGTGCCTA | 57626 |
rs9529676 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | KLHL1 | GRCh38.p7 | 13:70067054 | TAACATTAAGAGAAC[A/G]AAGTCCTGTACTCCA | 57626 |
rs9529677 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL1 | GRCh38.p7 | 13:70071901 | cttcagccccccaaa[A/G]ctggaaacagaagag | 57626 |
rs9529678 | snp | C/T | 0.219648 | 0.248151 | intron-variant | KLHL1 | GRCh38.p7 | 13:70072572 | tcaaatagaaaaatg[C/T]ataacaataattata | 57626 |
rs9529679 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:70086594 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57626 |
rs9529680 | snp | A/G | 0.447162 | 0.153712 | intron-variant | KLHL1 | GRCh38.p7 | 13:70096993 | TTCTGCTCCAAATGC[A/G]GTGTAAAATGAATCC | 57626 |
rs9542032 | snp | C/T | 0.0314385 | 0.121371 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69700913 | AGAATCACTAGCTTC[C/T]ATGCTTACACTGAAC | 57626 |
rs9542033 | snp | A/G | 0.0314385 | 0.121371 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701176 | TGTTCTCATAGCTTA[A/G]GAAAATGAGGCAGAA | 57626 |
rs9542034 | snp | G/T | 0.298144 | 0.245321 | utr-variant-3-prime | KLHL1 | GRCh38.p7 | 13:69701204 | GAAGCAGGTTTGTTT[G/T]AATAAAGCATAATTC | 57626 |
rs9542035 | snp | C/G | 0.0368353 | 0.130617 | intron-variant | KLHL1 | GRCh38.p7 | 13:69704806 | TGAGTAATATGATAA[C/G]CTAAAAAGGTTGGCC | 57626 |
rs9542036 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | KLHL1 | GRCh38.p7 | 13:69710802 | CTAGTTGCCAGGTTT[G/T]TTTGTTTGTTTGTTT | 57626 |
rs9542037 | snp | C/T | 0.499824 | 0.00938333 | intron-variant | KLHL1 | GRCh38.p7 | 13:69712256 | AAGAAGTCTTTCACA[C/T]CTCATTTTTTTTTTT | 57626 |
rs9542038 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL1 | GRCh38.p7 | 13:69713352 | atggtattagccgtc[A/G]tttctttcttctcat | 57626 |
rs9542039 | snp | A/G | 0.497668 | 0.0340657 | intron-variant | KLHL1 | GRCh38.p7 | 13:69717191 | AATAAAATGTGATCT[A/G]TCCATCTCTCTACAA | 57626 |
rs9542040 | snp | A/C | 0.499801 | 0.00998203 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718540 | GTAGAGTTACTTATA[A/C]CAATTGATAAACCAA | 57626 |
rs9542041 | snp | A/G | 0.497241 | 0.037038 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718630 | GGAAATATTACCATG[A/G]TCTTACTAAGGACTC | 57626 |
rs9542042 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718686 | ATAGTTCTAAGTAAC[A/G]CACAGCCCAAAGAGA | 57626 |
rs9542043 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | KLHL1 | GRCh38.p7 | 13:69718832 | ACCTATGTTTCCTTC[A/T]TACACCAGAATTATT | 57626 |
rs9542044 | snp | A/T | 0.470618 | 0.117591 | intron-variant | KLHL1 | GRCh38.p7 | 13:69720918 | AGGGAGAATATGATT[A/T]GTTTGTGTTTTAATG | 57626 |
rs9542045 | snp | A/C | 0.173643 | 0.238054 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722135 | CGTACATAGTTTATA[A/C]ATAAACATGATATGA | 57626 |
rs9542046 | snp | G/T | 0.187053 | 0.241946 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722222 | TCATAAACATTACTC[G/T]GATAAATTATACTAT | 57626 |
rs9542047 | snp | A/G | 0.499793 | 0.0101816 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722434 | aatctgaacagaccT[A/G]TATCTATCTAATCTA | 57626 |
rs9542048 | snp | A/G | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69722573 | cagcactaaccatca[A/G]agaaatgcaaatcat | 57626 |
rs9542049 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL1 | GRCh38.p7 | 13:69722606 | ccacaatgagatatc[A/G]cctcactccagttgc | 57626 |
rs9542050 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724435 | taaagaagaattaat[A/G]ctaattcttctcaaa | 57626 |
rs9542051 | snp | A/G | 0.184838 | 0.241358 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724555 | aaaaacaaacaaaca[A/G]acaaaaactagaggc | 57626 |
rs9542053 | snp | A/C | 0.0329967 | 0.124213 | intron-variant | KLHL1 | GRCh38.p7 | 13:69724974 | cccaagcctcaccag[A/C]gtgatttggagcaac | 57626 |
rs9542054 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725585 | ATGAGTATTGGTGGA[C/T]AATTAGCCAAACTCA | 57626 |
rs9542055 | snp | A/C | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69725592 | TTGGTGGACAATTAG[A/C]CAAACTCATTCATAC | 57626 |
rs9542057 | snp | C/T | 0.48491 | 0.0855403 | intron-variant | KLHL1 | GRCh38.p7 | 13:69727521 | TGGAATGATTTGGTA[C/T]GGCTGGGACATCAGG | 57626 |
rs9542058 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69728557 | cctgtaattctagca[C/T]tttgggaggccaagg | 57626 |
rs9542059 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | KLHL1 | GRCh38.p7 | 13:69729915 | CTCTGATATTTTTTA[C/T]GAAGAAAGATACTAG | 57626 |
rs9542060 | snp | A/G | 0.5 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69730269 | TACTAACACTTTAAt[A/G]tgtgtgtgtgtgtgt | 57626 |
rs9542061 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731210 | ACATAATTTTTCTAT[A/G]AATGTCATTAAAAGG | 57626 |
rs9542062 | snp | A/G | 0.490508 | 0.0682328 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731604 | TATAGTGTAAAGTTC[A/G]ATAGCGAACACTTTA | 57626 |
rs9542063 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69731903 | AAAGTAAAACAAAGC[A/G]TGTAGAAGTTTTTCC | 57626 |
rs9542064 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732077 | AGGAGGGGAGTCAAA[G/T]AAAGATATCGTGTAA | 57626 |
rs9542065 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732127 | ATTTTAAGTCTGCAT[C/T]GGAGATACAAACGAT | 57626 |
rs9542066 | snp | C/T | 0.093417 | 0.194889 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732229 | CAGTCTTAAAACACA[C/T]ATAGAACCATTAACG | 57626 |
rs9542067 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732479 | ACtttttaagctgtt[G/T]tctctcaggtctaca | 57626 |
rs9542068 | snp | C/T | 0.436408 | 0.16659 | intron-variant | KLHL1 | GRCh38.p7 | 13:69732699 | CCATCCTTTTCTCAC[C/T]GTAGCAGCCCTGTAG | 57626 |
rs9542069 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69738368 | agcaacatgtctcca[G/T]caagtgcacagaact | 57626 |
rs9542071 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KLHL1 | GRCh38.p7 | 13:69749987 | CTGTTTGCCTGTTAG[A/C]CATTAATTGTATCTT | 57626 |
rs9542072 | snp | A/G | 0.0633504 | 0.166319 | intron-variant | KLHL1 | GRCh38.p7 | 13:69750569 | AATCACCCCCAAAAT[A/G]TATAAGCATATAATA | 57626 |
rs9542073 | snp | A/G | 0.210301 | 0.246828 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753561 | GTATTAGTAGGGCCA[A/G]ATCTAGATTTTATTT | 57626 |
rs9542074 | snp | A/C | 0.443866 | 0.157848 | intron-variant | KLHL1 | GRCh38.p7 | 13:69753744 | ATTCTCTACTGTATT[A/C]TAACAGGGTTCTGTT | 57626 |
rs9542075 | snp | G/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69754014 | GCTAATTTTTTTTTT[G/T]GTTTTTAGTAGAGAT | 57626 |
rs9542079 | snp | A/G | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69759032 | tggaaattaagggca[A/G]ggattgtctatgtcc | 57626 |
rs9542084 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69771677 | GCCAAGAGATACTAA[C/T]GGTGAAGATATGTGG | 57626 |
rs9542086 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | KLHL1 | GRCh38.p7 | 13:69775531 | AAACAAGAACTGTTT[A/T]CTATTAGGGCTTACA | 57626 |
rs9542090 | snp | A/G | 0.498346 | 0.0287064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69797824 | ACAGAGCGAGACTCC[A/G]TCTAAAAAAAAAAAA | 57626 |
rs9542091 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | KLHL1 | GRCh38.p7 | 13:69798986 | ctcagctactcagga[C/G]gctaaggcaagagaa | 57626 |
rs9542092 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KLHL1 | GRCh38.p7 | 13:69799149 | ACTATATTTGACCGA[C/T]GATGGCAGAAGAAAG | 57626 |
rs9542094 | snp | C/T | 0.26078 | 0.249767 | intron-variant | KLHL1 | GRCh38.p7 | 13:69824871 | TCACTTAAAGGACCA[C/T]TTAAGATTTGCACAT | 57626 |
rs9542095 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL1 | GRCh38.p7 | 13:69825710 | GCACATGTTTTATCC[C/T]AGGACTACAGGGCTG | 57626 |
rs9542096 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL1 | GRCh38.p7 | 13:69827724 | gacagagcgagaccc[C/T]gtctcaaaaaaaaaa | 57626 |
rs9542097 | snp | A/C | 0.353371 | 0.227628 | intron-variant | KLHL1 | GRCh38.p7 | 13:69831430 | aacagaccaataaca[A/C]ggagcaagattgaaa | 57626 |
rs9542098 | snp | C/T | 0.141934 | 0.225437 | intron-variant | KLHL1 | GRCh38.p7 | 13:69843408 | CTCATGACATAGATT[C/T]AAATATCTTTAAATT | 57626 |
rs9542102 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL1 | GRCh38.p7 | 13:69876803 | aacactttgggaggc[C/T]gaggcgggtggatca | 57626 |
rs9542103 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69880082 | AAATGGCACTCATAT[C/T]GTAGAAATATCTCTG | 57626 |
rs9542106 | snp | C/T | 0.194278 | 0.243711 | intron-variant | KLHL1 | GRCh38.p7 | 13:69897101 | CCCTTGAAAGGATAC[C/T]TGATAATTTATTTAA | 57626 |
rs9542107 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903266 | aactgcagccagaac[C/T]caccacacccccact | 57626 |
rs9542108 | snp | A/G | 0.185472 | 0.241529 | intron-variant | KLHL1 | GRCh38.p7 | 13:69903767 | ctgcctcagcctccc[A/G]agtagctgggattac | 57626 |
rs9542109 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906042 | GGAAATAAAGTAACC[A/G]TAAAGAATTTTGATT | 57626 |
rs9542110 | snp | C/T | 0.497359 | 0.0362457 | intron-variant | KLHL1 | GRCh38.p7 | 13:69906506 | TTTAGTGTTGATATA[C/T]TGAGTGTTTTCTTTA | 57626 |
rs9542111 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | KLHL1 | GRCh38.p7 | 13:69911354 | TAAATCAAAGAGTGA[C/T]ATTTTTGGAATTCTG | 57626 |
rs9542112 | snp | C/T | 0.497959 | 0.0318836 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915239 | cagaattggaaaaaa[C/T]tactttcaagttcat | 57626 |
rs9542113 | snp | G/T | 0.497959 | 0.0318836 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915240 | agaattggaaaaaac[G/T]actttcaagttcata | 57626 |
rs9542114 | snp | A/G | 0.484561 | 0.0864924 | intron-variant | KLHL1 | GRCh38.p7 | 13:69915759 | ggatctaattaaact[A/G]aagagcttctgcaca | 57626 |
rs9542116 | snp | A/G | 0.451483 | 0.148002 | intron-variant | KLHL1 | GRCh38.p7 | 13:69924740 | gagagaagagcagcc[A/G]ccctttagggagccc | 57626 |
rs9542117 | snp | A/G | 0.46137 | 0.133501 | intron-variant | KLHL1 | GRCh38.p7 | 13:69926454 | TAAAATAAGAACCTC[A/G]ATTTCCTCATAaaac | 57626 |
rs9542118 | snp | C/T | | | intron-variant | KLHL1 | GRCh38.p7 | 13:69926944 | agagtgagactccat[C/T]tcaaaaaaaaaaaaa | 57626 |
rs9542119 | snp | C/T | 0.315758 | 0.241197 | intron-variant | KLHL1 | GRCh38.p7 | 13:69927627 | tccaaagaggatata[C/T]aaatgtccaataaat | 57626 |
rs9542120 | snp | C/T | 0.383246 | 0.211531 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933040 | GTACCCAGCCTGCCA[C/T]ATTTTTACTTAGTTC | 57626 |
rs9542121 | snp | C/T | 0.307176 | 0.243374 | intron-variant | KLHL1 | GRCh38.p7 | 13:69933054 | ACATTTTTACTTAGT[C/T]CTTTTCAACATTAAA | 57626 |
rs9542123 | snp | C/T | 0.104504 | 0.2033 | intron-variant | KLHL1 | GRCh38.p7 | 13:69935235 | GGTACATAGTTCACC[C/T]ACTGGTGAACTTGGT | 57626 |
rs9542124 | snp | C/T | 0 | 0 | intron-variant | KLHL1 | GRCh38.p7 | 13:69939340 | ATATACATATACATA[C/T]ATATATATATATATA | 57626 |