| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs58655730 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056106 | TTTTTCTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs58719116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916499 | CCATCCCACAATTTA[C/T]TGTCTCTTGAAGCTC | 114792 |
| rs58797465 | snp | G/T | 0.213937 | 0.247385 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042263 | ATGCTAAAATGAAAG[G/T]GTCTTCTCTTGAGAT | 114792 |
| rs58843276 | in-del | -/AAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904357 | AAAAAAAAAAAAAAA[-/AAA]GAAAAGAAAAAGAAA | 114792 |
| rs58976345 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097860 | TGTTCTGCCCTGTTT[C/T]GCACAGTAACCAGCA | 114792 |
| rs59057028 | in-del | -/A | 0.467744 | 0.122832 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027162 | GGGAGATTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs59100292 | snp | A/T | 0.0741063 | 0.177655 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087179 | ATAAATATTATCAAT[A/T]TAGGCATTCAGCAGG | 114792 |
| rs59201674 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086915 | TCTAACTGAATTGAC[A/G]TCTGAGGCTAACCAT | 114792 |
| rs59234247 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083282 | GTGGTCCCAGCTGCT[C/T]GGGAGGCTGAGGCAG | 114792 |
| rs59241963 | in-del | -/ACAGAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928857 | GAGGCTCTTACAGAT[-/ACAGAT]TTTAAGGTTGCATAT | 114792 |
| rs59274190 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078926 | GCCAGGGAGCCACGG[C/T]GGTAGCCAAAACTAA | 114792 |
| rs59368141 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052742 | TCGATTGAGAAGGAC[C/T]TCTTAAATATTTTAA | 114792 |
| rs59411961 | snp | A/G | 0.252983 | 0.249982 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980366 | TTGAGGGCTTTTAAC[A/G]TGAAGGGAAGTTGAT | 114792 |
| rs59427252 | snp | A/G | 0.193966 | 0.243639 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065865 | AAAATAGGAACCAGC[A/G]CTTCCCAGGGAGACA | 114792 |
| rs59453908 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025987 | AAGAAAAAACTATTT[A/G]TCTTTCTTTTAATGA | 114792 |
| rs59455750 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939759 | TCAGAAATGCCGAGA[A/G]GCCATTGAGGAATGA | 114792 |
| rs59468865 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015843 | TTCATGGGTCGGCCC[A/G]TCACTATGTGCAGCC | 114792 |
| rs59522299 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018443 | AAAAAAAAAAAAAAA[-/A]TTATCTGGGCGTGTT | 114792 |
| rs59568420 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984715 | CCTTTTTTTGTTTTC[C/T]ATTTGCTTGGTGGAT | 114792 |
| rs59599012 | in-del | -/CT | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898119 | CACCCGGGAAGCTCT[-/CT]GTAAAGTTCTGTGCC | 114792 |
| rs59604151 | in-del | -/CT | 0.220843 | 0.248294 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007259 | CTTCGAGTTCTGAGA[-/CT]CTTTCTTTGGCTTCA | 114792 |
| rs59624219 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985087 | GACAAAATCTCTCAG[C/T]ATTTGCTTGTCTGTA | 114792 |
| rs59655968 | snp | A/C | 0.244898 | 0.249948 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057570 | CTCCCGCCCCCATTT[A/C]AAAAAATCAGATGGT | 114792 |
| rs59671212 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055803 | AACCTGTCTAAAAAA[A/C]AAAAAAAAAAAAAAA | 114792 |
| rs59688440 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950512 | GTTAAAAAAAAAAAA[-/A]CCCAGACACTTTGCT | 114792 |
| rs59804093 | in-del | -/A | 0.41408 | 0.188621 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037405 | TGAGGATAAAAAAAT[-/A]ACATTTGTTAAAATA | 114792 |
| rs59804866 | snp | A/G | 0.252983 | 0.249982 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973476 | AAAGTAAGTTGTGAA[A/G]GTTTCAAATATATTT | 114792 |
| rs59820477 | in-del | -/AGTACTG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132500 | TGCTTAATTTTTCTG[-/AGTACTG]GGAGGCAGTGATTAG | 114792 |
| rs59828741 | in-del | -/T | 0.306182 | 0.243605 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019965 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 114792 |
| rs59836505 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984670 | TTGGTTTAAAGTCTG[C/T]TTTATCAGAGACTAG | 114792 |
| rs59881885 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106729 | ACTCCGGGTGACAGA[A/G]GAGACCCTGTCTCAA | 114792 |
| rs59925256 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984703 | TTGCAACCCCTGCCT[G/T]TTTTTGTTTTCTATT | 114792 |
| rs59986399 | snp | C/G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122053 | AGTGAATATTATTGA[C/G/T]ATTATAAAGGGCAGG | 114792 |
| rs59988466 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984692 | AGAGACTAGGATTGC[A/G]ACCCCTGCCTTTTTT | 114792 |
| rs60002102 | snp | C/T | 0.147991 | 0.228242 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957250 | ATGGAGTCTGGATTA[C/T]ATCTAGATCATAAAT | 114792 |
| rs60012822 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981343 | TTATATCTTGTGCAC[A/G]TAGAGGTTTGTAGTC | 114792 |
| rs60070457 | in-del | -/CAAA | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039845 | AAACAAACAAACAAA[-/CAAA]AAACAAAGAAAGAAA | 114792 |
| rs60086952 | snp | A/G | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938217 | TGTATATTTACCAAG[A/G]GTGTCTCTGGCCACC | 114792 |
| rs60091311 | snp | C/G | 0.0923359 | 0.194016 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057625 | AAGATCTTGTTTTTT[C/G]ATATTTTGGATAACA | 114792 |
| rs60105971 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116050 | CTCAGCTTCTCTGAG[C/T]GGTGCCTCAGTTATT | 114792 |
| rs60158214 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934611 | ACTACTGAAACAGAG[A/G]TTATCATTTTCTACT | 114792 |
| rs60268275 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084612 | ATATAAAACTCTGGA[G/T]TTTAGTTAAGACAGG | 114792 |
| rs60303642 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953378 | CTCATGCCTGTAATA[C/T]CAGCACTTTGGTAGG | 114792 |
| rs60451608 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108568 | AGTGGCCCATTGTTT[G/T]GAATTTTCTTTGCCA | 114792 |
| rs60482205 | in-del | -/CACA | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068031 | ACACACACACACACA[-/CACA]TACACACACCATCAC | 114792 |
| rs60484445 | snp | C/G | 0.0663309 | 0.169604 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958860 | TAAGTTATGCAGAAG[C/G]CATGCAGGTGCACAC | 114792 |
| rs60521996 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018004 | TGGGTTTTATCTATT[A/G]TAAAACTGCCTAAGA | 114792 |
| rs60587934 | in-del | -/T | 0.498034 | 0.0312882 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953855 | TCATTAATAGTTGTC[-/T]TTTTTTTTTTTTGCT | 114792 |
| rs60717158 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912950 | AACTATCAGTTTTAC[A/T]GTGGTATTCATATTC | 114792 |
| rs60756737 | in-del | -/T | 0.0352966 | 0.128072 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946952 | TATACTTATTAACAG[-/T]GGGCACATATTTAAT | 114792 |
| rs60860969 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103198 | TGTGAACAATTTACT[A/G]AAACTTGAATTTATC | 114792 |
| rs60866808 | in-del | -/TTCCCTCTGTGGGTGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958742 | AGGCAATGTTTCCCC[-/TTCCCTCTGTGGGTGG]ACCCATTGGAAAGAA | 114792 |
| rs60892041 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101166 | GCCTAATGCTCTCAG[C/G]ATGCATGTTTACAAA | 114792 |
| rs60905639 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097788 | CGATTGTGCAGTGGG[A/G]AAGTATAAACGACAG | 114792 |
| rs60919663 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946254 | ATAGATATATAATAT[C/G]TATTTTCAGTTTCTG | 114792 |
| rs61012363 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984966 | CAGTTTCTTCCTAGC[C/T]TTGATGGTCTTTACA | 114792 |
| rs61127933 | in-del | -/TAGGTAC | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962723 | CTTTGCACTAGGTAC[-/TAGGTAC]ACTACATACACTATA | 114792 |
| rs61136544 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984743 | GATCTTCCTCCATCC[C/T]TTTATTTTGAGCCTA | 114792 |
| rs61136942 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939797 | GATGAAGTGGCAGGA[A/T]CTGGAAGGCTAAGAT | 114792 |
| rs61251376 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057559 | TTACACCCCCCTCCC[-/C]GCCCCCATTTCAAAA | 114792 |
| rs61338503 | snp | C/G | 0.211212 | 0.246973 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049280 | CTTCTCTTGTACCTT[C/G]GGGCCATTATTAAGT | 114792 |
| rs61348524 | snp | A/G | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938258 | AGTTATAGTTACAAG[A/G]TAATTCCATAGTGGA | 114792 |
| rs61479407 | snp | A/C | 0.210605 | 0.246877 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069553 | CACATGGTTTAATGT[A/C]GTTGGAAAATGTCTC | 114792 |
| rs61564418 | snp | A/T | 0.040671 | 0.13668 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934118 | ACTGGGCATTGTAGG[A/T]CCTTGCGTCAGAAAA | 114792 |
| rs61627039 | snp | C/G | 0.253264 | 0.249979 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955658 | AGACATACCCGAGGC[C/G]AGGCACGGTGGCTCA | 114792 |
| rs61697349 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976586 | GATATATATATATAT[-/A]TTTTGTTTTGTTTTG | 114792 |
| rs62413860 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939760 | CAGAAATGCCGAGAA[A/G]CCATTGAGGAATGAT | 114792 |
| rs62413861 | snp | C/T | 0.156319 | 0.231784 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941997 | GAATGCAGAAAAAGA[C/T]TGGCATATGTACTGT | 114792 |
| rs62413862 | snp | A/G | 0.115788 | 0.21092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942210 | TGCAGCCCAAGATCT[A/G]CTGGCCCCACTTGTC | 114792 |
| rs62413863 | snp | C/T | 0.156319 | 0.231784 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942391 | CTCAATACCCATTTC[C/T]TCCATGAAACCATTC | 114792 |
| rs62413864 | snp | C/T | 0.156319 | 0.231784 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942798 | GTTATTCTGATGCCA[C/T]CACCTCCCTTTCTAC | 114792 |
| rs62413865 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943527 | CACAAACTGATTTAA[C/T]TGGATTCCTCCACAT | 114792 |
| rs62413868 | snp | G/T | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948647 | AATATCTTGGTTAGA[G/T]AATACACTTTTTTAA | 114792 |
| rs62413869 | snp | C/T | 0.114036 | 0.209795 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948741 | TTTAACTTCAGTCAC[C/T]GTGATGGATTTGACA | 114792 |
| rs62413870 | snp | A/G | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951868 | CTGTTTCTTTAGATA[A/G]CAGCAGGTCCTGGAG | 114792 |
| rs62413871 | snp | C/T | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953001 | TGGTCCCCTGCCTGC[C/T]AACTTACCATAAAAA | 114792 |
| rs62413872 | snp | A/G | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953173 | AGAAGACCCCATCAG[A/G]TGATTACAAATTTGA | 114792 |
| rs62413874 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957723 | AAGAGCTGAAAAGGC[A/G]TGTGCTAATGTGACT | 114792 |
| rs62413875 | snp | C/G | 0.154993 | 0.231244 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959611 | ATTACCTCTTTAAAG[C/G]CCAAATCTCCAACAC | 114792 |
| rs62413876 | snp | A/G | 0.154993 | 0.231244 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960099 | CCATACAGAATAGGG[A/G]TAGTAAATAAGCTAG | 114792 |
| rs62413877 | snp | G/T | 0.21875 | 0.248039 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967474 | ATGTGTATATATATA[G/T]AGAGAGAGAGATAGG | 114792 |
| rs62413878 | snp | A/G | 0.095934 | 0.196885 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970424 | AGGATCGTAGCATTT[A/G]CTGTTCTCCTGCCTG | 114792 |
| rs62413879 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977908 | AGAGTATCTGTAAAG[C/T]GGCCTTTTAGTTCCA | 114792 |
| rs62413889 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983205 | TTGCATATGTTGAAC[C/T]AGCCTTGCATCCCAG | 114792 |
| rs62413892 | snp | G/T | 0.0955749 | 0.196603 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985056 | TCAGGAGCTCTTGTA[G/T]GGCAGGCCTGGTGGT | 114792 |
| rs62413894 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038872 | GAGGCAGGTGGATCA[A/C]TTGAGGTCAGGAGTT | 114792 |
| rs62413895 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040918 | CTTCACCTTCGCCTT[C/T]GCCTTCCACCATTAT | 114792 |
| rs62413896 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059096 | CGTGACCTAGAACAC[A/G]TGGGCTTATTAGTTC | 114792 |
| rs62413897 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062728 | GCTGGGGATACAAAA[C/T]AGACTAAGTCCCTGC | 114792 |
| rs62413898 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074257 | CAGGAGGTCTGGGGA[A/G]GGCCTAAGAACCTGT | 114792 |
| rs62413899 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081624 | AGGGAAGCCTTTACT[A/G]ACTTTCCACTCCAAG | 114792 |
| rs62413900 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085635 | AGGGATGTTTTTTTC[C/T]TGATAAAAATTGTTT | 114792 |
| rs62413906 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111064 | CCAACCACCTGTTAC[A/G]TCTGGGACTGGGTCC | 114792 |
| rs62413907 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117397 | TCTTGGTTCTGTTCT[C/G]TAGAACACAGAATGA | 114792 |
| rs62413908 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119738 | TTTCCAATTAACAGT[A/C]TGGCTTCCTGTATAC | 114792 |
| rs62413909 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122786 | TGTTTTGCATATGAG[A/G]AAGCTGAGCATGGCT | 114792 |
| rs62415286 | snp | A/G | 0.0581099 | 0.160244 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896910 | TGTAATATCCTAAAC[A/G]CTTAACACAAACGCT | 114792 |
| rs62415287 | snp | A/G | 0.0505692 | 0.150756 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898016 | TCGGGGCGAGTGACG[A/G]CTCCCACGAGGGCCG | 114792 |
| rs62415288 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903261 | TAAATTGAAAGAAAA[A/T]ATATATAAATATATA | 114792 |
| rs62415289 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909970 | TGTGACAGGTGGGAA[A/G]GGAAAAATGGCAGGA | 114792 |
| rs62415290 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911268 | GATAGAAAATCTTGA[C/T]GTCTCTTGCGAAGAA | 114792 |
| rs62415291 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911277 | TCTTGACGTCTCTTG[C/T]GAAGAAAAAGACTTC | 114792 |
| rs62415292 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912483 | CCCTTTACTGGAATA[C/T]TCTTTTCTCCATTAT | 114792 |
| rs62415293 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913024 | TGCAAAATTATTTCA[A/G]TGTTTGATTGCTCTC | 114792 |
| rs62415294 | snp | C/T | 0.0948562 | 0.196037 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917725 | GATCAATTCCTGTGA[C/T]GGGCTTAAGAGACTT | 114792 |
| rs62415295 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920062 | ACAGAAAGAGTTTCA[A/G]GGAAAAAAACCCGAT | 114792 |
| rs63742563 | in-del | -/CTG | 0.461148 | 0.133852 | intron-variant | KLHL32 | GRCh38.p7 | 6:97008046 | AGGGCAGTGGCATTC[-/CTG]CTGCACCTCCTCATG | 114792 |
| rs63751061 | snp | C/T | | | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896790 | AGCTGCTGTCGTTTC[C/T]AAAAGATGTGTATGT | 114792 |
| rs66490382 | in-del | -/A | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010127 | AGGCACTGATTTGAC[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs66545723 | in-del | -/ACCT | 0.429837 | 0.173662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042612 | CAAATTTATCACCTC[-/ACCT]ACCTACCTATTTTTT | 114792 |
| rs66706487 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977555 | AATGGGAATATAAAC[-/T]AATTTAATTGTGTTG | 114792 |
| rs67053923 | snp | G/T | 0.26078 | 0.249767 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926209 | AATTTTGTTTTCCTT[G/T]GATATTTGTTCATCT | 114792 |
| rs67372979 | in-del | -/A | 0.479744 | 0.0985793 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089779 | AATGAAACTCCAGCT[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs67506309 | in-del | -/ACTAGGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962715 | GTGTCAGCCTTTGCA[-/ACTAGGT]CTAGGTACACTACAT | 114792 |
| rs67578061 | in-del | -/T | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962857 | GTGCAAACAGCTTCA[-/T]TTTGTAAAATGTGTG | 114792 |
| rs67810395 | snp | C/T | 0.253824 | 0.249971 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963446 | AATTATGAAAATGTT[C/T]TTTATAAATGTAAAT | 114792 |
| rs67945805 | in-del | -/T | 0.273587 | 0.248885 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030862 | TATGACACTGTAGGG[-/T]TGGTAGGACATCATC | 114792 |
| rs68086851 | in-del | -/TGTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115993 | ATTTGGACTTTGACT[-/TGTT]GTTCTTCTGCTGTCC | 114792 |
| rs68098379 | in-del | -/T | 0.258288 | 0.249863 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931881 | GAGTAGGCTTTTTTT[-/T]CATAATGATTTTGTA | 114792 |
| rs68171946 | in-del | -/T | 0.479421 | 0.0993283 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932257 | AATATGGAATCAATG[-/T]TTTTTTTTTCCATGA | 114792 |
| rs71012578 | in-del | -/AA | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932221 | AGGCTTTGAAATCTC[-/AA]AAAAAAAAAAAAAAA | 114792 |
| rs71012579 | in-del | -/A/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954312 | AAAAAAAAAAAAAAA[-/A/AA]ATTGAAGGAAAGAAA | 114792 |
| rs71012580 | in-del | -/TTTTTTTTTTTTTTTTTTTTT | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055822 | AGAAATAAGAAGGGG[-/TTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 114792 |
| rs71012582 | in-del | -/TTGTTT | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138549 | TTTGGGGTTTTTTTG[-/TTGTTT]TTGTTTTTGTTTTTG | 114792 |
| rs71545724 | in-del | -/TTTATATA | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953788 | ACAATCTAAATGTTA[-/TTTATATA]ATCAAACCATGATTA | 114792 |
| rs71562313 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931687 | CAAGTTTAGTGATTG[G/T]TAAAGACAGAAAATC | 114792 |
| rs71562314 | snp | A/C | 0.257732 | 0.24988 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933590 | ATTTCCCCTTTGTAT[A/C]TGGAGCCTCATGGTT | 114792 |
| rs71562315 | snp | A/G | 0.362941 | 0.223034 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963046 | TAGGGGAGGGGGAAA[A/G]ATCTTTTTTCCTCTA | 114792 |
| rs71562316 | snp | A/G | 0.252702 | 0.249985 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982692 | TGTTTGTCTGTTACT[A/G]GTGCATAAGAATGCT | 114792 |
| rs71562319 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051010 | CTCCATCTCAAACAA[A/C]CAAACAAACAAACAA | 114792 |
| rs71562320 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051022 | CAAACAAACAAACAA[A/C]CAAAAAACACATGTG | 114792 |
| rs71562321 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055477 | CCATCAGTTTCTCCT[C/T]TACTGCATTCTATTG | 114792 |
| rs71562322 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055899 | AGAGCTTATGAAAAG[G/T]GTTACATAAAGTTAT | 114792 |
| rs71562323 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136651 | AGATCACCTCTACTG[G/T]TATCTTCATTTACTA | 114792 |
| rs71701485 | in-del | -/CA | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924802 | ACACACGCACGCAGG[-/CA]CACACACACACACAC | 114792 |
| rs71784283 | in-del | -/TAAA | 0.270621 | 0.249148 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040028 | GGCATTGATAAAATT[-/TAAA]TAAATAAATAAAATT | 114792 |
| rs71820477 | in-del | -/CAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931125 | AAACAAACAAACAAA[-/CAAA]AAACACTCCTCAAAT | 114792 |
| rs71938480 | in-del | -/TTAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025985 | AGAAGAAAAAACTAT[-/TTAT]CTTTCTTTTAATGAT | 114792 |
| rs72057472 | in-del | -/AG | 0.483563 | 0.0891524 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138250 | CTGTGCTATATAAGA[-/AG]AGAGAGGCCAGGCAC | 114792 |
| rs72099257 | in-del | -/TACAGA | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928850 | GGCTAAGGAGGCTCT[-/TACAGA]TACAGATTTTAAGGT | 114792 |
| rs72275621 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943386 | TTTCCAAGAAGAAGT[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs72308130 | in-del | -/A | 0.15665 | 0.231917 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958830 | GAAGGAGTGCCAAGG[-/A]AAAAAAAAATCACCC | 114792 |
| rs72484510 | in-del | -/ACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068010 | GAAAACTTCATACAG[-/ACAC]ACACACACACACACA | 114792 |
| rs72924718 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914606 | CAAAGCCTCAACACC[A/G]TTCCTTTCCTTTCCA | 114792 |
| rs72924743 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931357 | TCAAAGTCACCCCCC[A/G]GCTCATGGGCTTAAG | 114792 |
| rs72924749 | snp | A/T | 0.257732 | 0.24988 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933221 | AGGGATGAAATTCCC[A/T]TACCCCTCAAAACAC | 114792 |
| rs72924759 | snp | C/G | 0.259397 | 0.249823 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936889 | GCCTCCTGCCTACCC[C/G]CAGGCCCACTGTCTT | 114792 |
| rs72924765 | snp | C/T | 0.0970103 | 0.197722 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938509 | TGCTGCTTCTGACTG[C/T]TCTGGTCCTCCCTGA | 114792 |
| rs72924793 | snp | A/C | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951001 | ACTCAGTTTGAACAA[A/C]AAAAAAGTACTTCTC | 114792 |
| rs72924795 | snp | A/G | 0.243919 | 0.249926 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951556 | GATACCTTAGAGTTT[A/G]CCATCACTACCATCA | 114792 |
| rs72924797 | snp | A/G | 0.243919 | 0.249926 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951880 | ATAGCAGCAGGTCCT[A/G]GAGTAGCGTTGTTTT | 114792 |
| rs72924798 | snp | A/G | 0.254664 | 0.249956 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951881 | TAGCAGCAGGTCCTG[A/G]AGTAGCGTTGTTTTG | 114792 |
| rs72926815 | snp | C/T | 0.252983 | 0.249982 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961485 | CTTACTTTTTTCCTA[C/T]CCCTTTTGTTACTGG | 114792 |
| rs72926825 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965470 | CTTATTAGTTAGATG[A/C]CATTTAATTTGAGAT | 114792 |
| rs72926883 | snp | C/T | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997483 | CCAGGCATGGTGGCT[C/T]GTAAATGTAATCCCA | 114792 |
| rs72926885 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999912 | GGGCTCCTAAAACAT[C/T]ACCACTACAGCTTCT | 114792 |
| rs72930919 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048759 | ATCTGCTTTCTCATG[A/G]ACCATCCCTTCAGGG | 114792 |
| rs72930965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061776 | CCTTCGAGGCAGGTG[A/G]CAGATAAATTCACCA | 114792 |
| rs72930973 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068240 | ATATTGTTTTATTAA[A/C]AACCATTCTTTATGT | 114792 |
| rs72930989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081109 | CAATAAGAGGGCACA[A/G]ACCACACCTCCAGGA | 114792 |
| rs72932651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110699 | AATCCTGATTCCATG[A/G]TTCAAAAAGGAAGTA | 114792 |
| rs72932671 | snp | A/G | 0.125415 | 0.216745 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126837 | AAATTTAATTTCACT[A/G]TTTCTTTTTACTTTT | 114792 |
| rs73488415 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137191 | TCAAACTAATCTTGA[A/G]AGATTCTCTAGGAAA | 114792 |
| rs73492830 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914605 | GCAAAGCCTCAACAC[C/T]GTTCCTTTCCTTTCC | 114792 |
| rs73492831 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915258 | ATCCACTCACTACCC[A/T]TCATCCAACAAATAT | 114792 |
| rs73492844 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930561 | CCTTCCCTCTGCCTC[C/G]CCTTTCCCCACTCCT | 114792 |
| rs73492846 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931654 | TAACATTACTTGAGA[C/T]ACCTAAAATAAGAAA | 114792 |
| rs73492866 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940779 | TAGTCATTCATTTAG[A/C]AGACGTTATTGGATG | 114792 |
| rs73492877 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942865 | AGAATCACTCCTTAC[A/G]GCAGAATGGCTTTCG | 114792 |
| rs73492880 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944699 | ACTTGTTCAAGTTGC[A/T]TGAGTAATAAGTTGT | 114792 |
| rs73492888 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948166 | TGAAGTCTAGCTATT[C/G]CGTGTTACTAATGCT | 114792 |
| rs73492895 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951586 | ATCTTACCATCATCA[C/T]CAAGACAATATTAAT | 114792 |
| rs73492898 | snp | A/T | 0.0718919 | 0.175435 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952136 | GATGGCATCCTGTCC[A/T]GGATGGGTTCCCGCC | 114792 |
| rs73492902 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953250 | ACTTACTTTATTTAC[A/G]TCCATATTTCTCAGT | 114792 |
| rs73494804 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954051 | TCCTTCACTATCACC[G/T]GAGAATTCCTATCAT | 114792 |
| rs73494810 | snp | A/T | 0.0471551 | 0.14613 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959154 | AGATGCTCCAAGAGG[A/T]CAGTAGTGGAGAGGC | 114792 |
| rs73494816 | snp | A/G | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960359 | TTGTCTTTCCCATCT[A/G]GAAGCCCAAAACCCC | 114792 |
| rs73494826 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972310 | CATTTTATATGTATG[A/G]TACATCTCAATTTGG | 114792 |
| rs73494829 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974705 | TGGTTAATTTTAAGA[C/T]GGTGATTTGTACCTA | 114792 |
| rs73494849 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990179 | GGCTTTTTGACTTGC[C/T]AGAGTTTTTGTACTA | 114792 |
| rs73494858 | snp | C/G | 0.28578 | 0.247426 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991871 | GCAGGGGCGGGGGAC[C/G]GCATTGAAAACAGGC | 114792 |
| rs73494867 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993549 | CCAGAATCATCAGAA[A/T]CATTTTAAGAGGGTG | 114792 |
| rs73494877 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994922 | GAATCTAGCAGCAGG[G/T]ACCTAATCTGTCTGT | 114792 |
| rs73494880 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995630 | AACACATTCTTTCCA[C/T]CTCAGGGCCTTTGCA | 114792 |
| rs73497008 | snp | C/T | 0.219049 | 0.248077 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002504 | TTTAGGGTCAGGGTA[C/T]ATGTGCAGGTTTGTT | 114792 |
| rs73499051 | snp | A/G | 0.219349 | 0.248114 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009559 | AAAAATGCATGCGAG[A/G]TGTTCCTTTGCTTTG | 114792 |
| rs73499052 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010377 | TGTCTCTCCCTCTCC[C/T]CCAGATCATAGCTGA | 114792 |
| rs73499057 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011037 | TTCTATTTCTAGATG[A/G]TAAATGAGAGCTTCC | 114792 |
| rs73499067 | snp | A/G | 0.211819 | 0.247067 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014514 | ATACTACAATAGTGA[A/G]ACAGTACACAGAATT | 114792 |
| rs73499072 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015562 | GTGGAACTCTGAATG[C/T]GAGAGAGATGATGTG | 114792 |
| rs73502803 | snp | C/G | 0.213937 | 0.247385 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023770 | GAGAACTAGGGGCCA[C/G]GAAAATCCTTGGCTA | 114792 |
| rs73502864 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054373 | AATACTTAATGAACA[C/G]CTACTATATGCTAAG | 114792 |
| rs73502873 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058713 | TTTTTGTTCTTTGAC[C/G]TCTCCTTTCTTTCTG | 114792 |
| rs73502876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062709 | GCTGAACATTGTTCT[A/G]AGTGCTGGGGATACA | 114792 |
| rs73502885 | snp | A/C | 0.229136 | 0.249128 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069195 | CAAGGAGGAACATAA[A/C]GGGAACAGGAGGGAG | 114792 |
| rs73505011 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083954 | TGCTTAAGACTCACA[A/G]AGCCCATCTGCCCCA | 114792 |
| rs73505013 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084090 | CAGTAAGGAGTTCTT[A/G]ATACTCTCAGGTAAC | 114792 |
| rs73505024 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090218 | ATAATAAGACATCCT[A/G]CTATTCCTACATTAG | 114792 |
| rs73505025 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090365 | ATTCATTTTATATCT[C/T]GAGAGACATAAGCCA | 114792 |
| rs73505029 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096137 | TCATTCTCACACCCA[A/G]CGTAGCTAATAAAAT | 114792 |
| rs73505043 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117152 | TAGATTTGCTAATGG[A/G]CCCCTTAACAAAAAT | 114792 |
| rs73758055 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914478 | CTAGCATTTGAAATG[G/T]GGCTTTACCAAATAG | 114792 |
| rs73758056 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918840 | ATGGGGCAGGAGAGG[A/T]TATAGTAAAAGAAAA | 114792 |
| rs73758057 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920429 | ATGTGTGAGTTCCCC[A/C]GGTTAGAGAGTGACA | 114792 |
| rs73758058 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921740 | ATGTAGTTTTAGCTA[A/G]AAATCTGATCTGTGT | 114792 |
| rs73758059 | snp | A/C | 0.0383715 | 0.133092 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923142 | AAATGCAATTATAGT[A/C]TTTGCTCTATTTAAT | 114792 |
| rs73758061 | snp | G/T | 0.0718919 | 0.175435 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925652 | AAGCAGATGATTTAA[G/T]TGTGTTTCCCCACAC | 114792 |
| rs73758062 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926071 | AGGTCTCGGGTGTCT[A/G]TTGGGTGAACTTGTA | 114792 |
| rs73758063 | snp | G/T | 0.0629771 | 0.165899 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926883 | AAAATTGTATCTGGG[G/T]CATATCTAGCCTGTG | 114792 |
| rs73758064 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927505 | AAGCTGCCATTTTCT[C/T]GTGTTTCTCCTAGAG | 114792 |
| rs73758065 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932575 | AATTTCCCCCCCCCC[C/T]TTTTTTTTTTTGAGA | 114792 |
| rs73758066 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936571 | ACCCAGAATCTGACC[A/G]TATGTCACAACTTCC | 114792 |
| rs73758067 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943503 | TAACTTCACATCAGC[G/T]GTAAATCCCACAAAC | 114792 |
| rs73758068 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945358 | CTTAGAGCAGAAATC[C/T]CAGCCTGTACCCTAA | 114792 |
| rs73758069 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950183 | AGCACATTTTTAATG[A/G]CAGAGGCAAGTGTTT | 114792 |
| rs73758070 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950878 | AGAAGACATTCTTAT[A/G]TCTGAGAGCCCATGA | 114792 |
| rs73758072 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950901 | GCCCATGAGATGATA[A/G]TGAGAAAATGCAATT | 114792 |
| rs73758075 | snp | G/T | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954796 | CCATGTAGTGCAGAT[G/T]AGGGGAAGGGACCTA | 114792 |
| rs73758076 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958720 | CACATCTCTCAGCAC[A/G]TGGAGCTAGGCAATG | 114792 |
| rs73758077 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960450 | ACTCATAACTAGGGG[C/T]TCCCACATGTATTTA | 114792 |
| rs73758082 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975642 | ATGCACATCCAGAGG[A/C]AGTTTTGCACTCAGA | 114792 |
| rs73758106 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090036 | GGCAAAGAGGGACCA[C/T]GTCACCTGATTTGGG | 114792 |
| rs73758110 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101219 | AAAATGTATAAATGT[A/G]CCAGCAACATTTAAA | 114792 |
| rs73758111 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102420 | AATTGGTTTTCTCTC[A/G]TTTTCCAGTGTAGTT | 114792 |
| rs73758113 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119084 | CACTTCAATAATTAT[C/T]TTGTCCTCTGGGAAA | 114792 |
| rs73758115 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123820 | CATGTGGCATCGTAA[C/T]CCAGAGCAGACAAAT | 114792 |
| rs73758117 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125724 | GAGGTTGCAGTGAGC[C/T]GAGGTTGCACCATTG | 114792 |
| rs73758118 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131188 | ACATCCTCATATGGC[A/T]GAGAGGCATGTCAAG | 114792 |
| rs73758119 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132832 | ACTGAAGAAAGAGAT[A/G]TTTATGTTTAGAAAG | 114792 |
| rs73758120 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136612 | GCAGCTGCGTAAGTG[G/T]GCAAGTGATTAGTCT | 114792 |
| rs74272660 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032944 | AGCTTTTTTTTTTTT[-/TT]ATCTATAGCCACACT | 114792 |
| rs74317452 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091216 | CCTGTCTGGAAGAAA[A/G]AAAACAAAACAAAAC | 114792 |
| rs74317470 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067579 | CTTTCCCAAGAAAGG[A/G]AACCACATATATTGA | 114792 |
| rs74322147 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116079 | TTGGCAATTCACTGA[G/T]TTTTATTGACAGAAC | 114792 |
| rs74351655 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037361 | ATATTGTCCATCTTA[C/T]ACATATTAATTTAAA | 114792 |
| rs74358108 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915937 | TTCCTTTCCCAAAAA[-/A]AGAAAGAGATCAACC | 114792 |
| rs74375949 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104093 | CACAAGTAGAGAAGA[C/T]ATCACAGGTTATTAA | 114792 |
| rs74378018 | snp | C/T | 0.147321 | 0.227941 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960315 | ACAATTCTCGTTTAC[C/T]GTACTTTTCCTGGTC | 114792 |
| rs74385757 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072542 | GGGCCTGTCTTTATT[A/G]TGAAATGTGCTATCT | 114792 |
| rs74443848 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025356 | TATCAGTATGCTTCT[C/T]ACTCAGAGAGCTGTG | 114792 |
| rs74457611 | snp | A/G | 0.185472 | 0.241529 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070025 | ATAACTTCTCCTCAA[A/G]ATTGAGGAGAAGTTA | 114792 |
| rs74474996 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939114 | CACCTTATTGGCTTG[C/G]ATGGCCCGCCTCTCC | 114792 |
| rs74484579 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081280 | TTTCCATGGGTTCAC[A/G]AGTGTAGGGGCTGGC | 114792 |
| rs74497251 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073640 | CCTTCTGCATGTACC[A/G]TAAGAGCTCCCTATG | 114792 |
| rs74506001 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942842 | TTTTTATTGTCCTCA[G/T]TCTGCAGAGAATCAC | 114792 |
| rs74542317 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908501 | GTAGTGAATCAGAAC[A/G]CTTGGAATCATGCAT | 114792 |
| rs74547565 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901344 | TTTTTTTTTTTTTTA[C/T]TTTAAATGGGGAAGG | 114792 |
| rs74562910 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049539 | TTTGGACTGCAGTTT[A/G]CCATGGGTAACTGAA | 114792 |
| rs74574934 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897249 | TAATTTTTTTAAAAA[A/T]TAAACATAATCATTT | 114792 |
| rs74602245 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129384 | GTAGAAAGAAAACTG[C/T]TAGGGTTATTTACCT | 114792 |
| rs74603560 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925310 | CCGTGGGACATCTAT[C/T]GAAAGAACTGGTTTC | 114792 |
| rs74629580 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965510 | TTTAGGATTTTTGCT[C/G]TCCATTCAGTTGTTG | 114792 |
| rs74688141 | snp | C/T | 0.030278 | 0.119257 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057869 | GTAAGAGTTTTCTAG[C/T]TTTGCATTTTACATC | 114792 |
| rs74696954 | snp | G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103226 | ATCTTTTTTTTTTTT[G/T]TTTTTGAGACGGCGT | 114792 |
| rs74702375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119112 | AAACATGCAGTGTTT[A/G]ACAAACCCAGTAATC | 114792 |
| rs74727494 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133767 | TATTCATATAGATGA[A/T]GTTAAAAAAGTCAGC | 114792 |
| rs74766426 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982295 | ATTGATCCCTTTATC[A/G]TTATGTAATGGCCTT | 114792 |
| rs74770485 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094319 | TCTAGAATTATTTAC[A/T]TTCTAAGGAGATGTC | 114792 |
| rs74771961 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976452 | GAAAATGTGGCACTG[C/T]AGTGCTTCATGTGGG | 114792 |
| rs74776706 | snp | A/G | 0.030278 | 0.119257 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959762 | CCTTTGGTTTCTATG[A/G]ATCAGGAAGGCCTAG | 114792 |
| rs74787311 | snp | G/T | 0.0901699 | 0.192244 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114331 | CCGGGAGCATTTTGT[G/T]CTGGGTGCCATGGAG | 114792 |
| rs74854911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127737 | TTGTCCTGTTGTAAC[A/G]TCCTTCTGGAAGGGG | 114792 |
| rs74928587 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906813 | TTTTTAGAGCTTTTG[A/G]TTCCATAGAAGCTCA | 114792 |
| rs74932422 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928291 | CTATTGAAAGATGGG[A/G]GTCTCCACCAGACAG | 114792 |
| rs74977491 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925724 | GTTTGTGAATTCGTA[A/G]CGTAAGAAGGTAGCA | 114792 |
| rs75002173 | snp | A/G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103776 | TTATAGACAAAAAAA[A/G/T]GTCACCTTGTTTTTC | 114792 |
| rs75013514 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108378 | TTCAAGCTTAAGCAC[C/T]GAAATATACCACAAA | 114792 |
| rs75048135 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954929 | ACTGGGTAGCTTAAA[A/C]AACAAGTATATTTCT | 114792 |
| rs75054798 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130070 | CCACTGATCTCAGGA[A/G]GTTAATTTTGGAAAG | 114792 |
| rs75082221 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030453 | TAGGCACTTAAAGTG[G/T]ATTATATACTCACAA | 114792 |
| rs75108344 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974934 | AGATGGATCTGCTGG[C/T]CAGAATCAGGGCTTG | 114792 |
| rs75121789 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037559 | AGGGAAAGATACTCC[A/G]TATTCATGGATAGGA | 114792 |
| rs75123193 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045029 | CTTTAGAGGCTTATT[A/G]AAACGTATGATATCA | 114792 |
| rs75145401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114647 | CTAATTAACATTCAT[A/T]TATTGAGCACCTACT | 114792 |
| rs75152480 | snp | A/G | 0.000848845 | 0.020584 | intron-variant, synonymous-codon, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105505 | CCCTGGCTTACCTCA[A/G]TGGGATGACAAGACT | 114792 |
| rs75158905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912836 | AGTTCCTCTGCATTG[C/T]AATTGCTGCTTATTT | 114792 |
| rs75182331 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032350 | AATGATTACCAATAT[A/G]GTGTTCCTTTATTGC | 114792 |
| rs75211068 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036480 | TGAAGGAGCAGTTAC[A/G]TCTTTCAGATATTAC | 114792 |
| rs75224922 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929903 | TCCCTTGCAAGGTTG[G/T]AGTCACCAACCTGAT | 114792 |
| rs75253101 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089453 | TATTAACTGTTTCTT[A/G]CTTTTAGTGAGAACT | 114792 |
| rs75262565 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953867 | GTCTTTTTTTTTTTT[G/T]GCTTATGTTTTTATA | 114792 |
| rs75277098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104845 | TTTCTGGTGCTTTTC[A/G]ATTTTATGGGAAAGT | 114792 |
| rs75282849 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933897 | GACACAGTAAGTGGA[C/T]TGGGAGAGCAAAAGC | 114792 |
| rs75322269 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930534 | GTAATAAAATCTCAG[G/T]ACTTATTAATTCCTT | 114792 |
| rs75324023 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093538 | TCTCATAAGTCAAAC[A/G]TTTTTATATATTACT | 114792 |
| rs75451737 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939083 | AAGCTAGCAAACAAC[A/T]ATGAGACATGGGCCA | 114792 |
| rs75465522 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967899 | TTCCAGAAACTGAGG[A/G]GCAGCCAATGAGAAA | 114792 |
| rs75474875 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063268 | GCAGTGATTGAATTC[C/T]GAAACTATTTTGAAG | 114792 |
| rs75494165 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057933 | GAAGGATTTGAGAGC[C/T]GTGTCCAGGTTCAAT | 114792 |
| rs75527223 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078496 | TTGAGTGTTATTACC[C/T]GGAAAAATCTGTAAT | 114792 |
| rs75548809 | snp | A/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012011 | TGCTAAACATTGAAT[A/T]AATTTGTAATCAATC | 114792 |
| rs75560056 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949077 | ACTCAATCACATCAC[A/G]ATGTTTTGTGCATTT | 114792 |
| rs75562073 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934393 | TTATTCCTACCTTCC[A/G/T]AGGACCAGCCAGGCC | 114792 |
| rs75562999 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067546 | TGTGGTAACCCATGG[A/C]CCCCAGACCATCACT | 114792 |
| rs75563613 | snp | A/C | 0.0168055 | 0.0901129 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011425 | GACAATTATTAATTA[A/C]TAATCACAAGTATGT | 114792 |
| rs75611798 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910542 | ATCTACAGCACTTCA[G/T]ATGGTGATTTGCAAA | 114792 |
| rs75619753 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075312 | TTTGAATATATCATT[A/G]CATACAGTTGTCCAT | 114792 |
| rs75633203 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939172 | GATGAAAGTTAGAAA[A/C]TACTGATGTATTCTG | 114792 |
| rs75660924 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027858 | AATTCAGATTAGATA[C/T]TATTTCCAGTAGGAG | 114792 |
| rs75670457 | snp | G/T | 0.127599 | 0.217986 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012906 | ATTGTTTTGGTTGTG[G/T]TTATTTTTCACTGCA | 114792 |
| rs75693171 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058832 | AAGGAGGCTGGTTGC[C/T]ACTCTAAGTGGCCTA | 114792 |
| rs75747996 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030171 | CTGCACATAGTTTGC[C/T]AGGTAAAAAGATCAT | 114792 |
| rs75753207 | in-del | -/AGTGAATG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950631 | GTGAATGAGTGAATG[-/AGTGAATG]GTTAGTGAACGACTA | 114792 |
| rs75762712 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075151 | AATTGTAGAATTCCT[C/G]TGTTACACAGCACAA | 114792 |
| rs75768443 | snp | C/T | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045735 | GCGTGTGTGTGTGCA[C/T]GCATGTGTGCGTGTA | 114792 |
| rs75867583 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979325 | TTTTTGTATAAGGTG[C/T]AAGAAAAGGGTCTAG | 114792 |
| rs75897871 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064277 | AACTAAAACTCAGTT[A/C]TTTTGCATTTTATAA | 114792 |
| rs75917130 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069027 | GTAAGGGAAACAGAG[A/G]AGGGGGGGGTCTGTT | 114792 |
| rs75917743 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135343 | GAGTGTCTTGCTCTG[C/T]CACCCAGGCTGGAGT | 114792 |
| rs75991629 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052560 | CCAGCAGGGCATTCC[A/G]GCGTGCAGGCTGTAG | 114792 |
| rs76015554 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047177 | AAAGCAAATTTTCCT[C/T]TTAATATTAATACAT | 114792 |
| rs76018218 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053224 | TTGAAATGAGGCAGA[A/G]AAGATAATAAGTAAC | 114792 |
| rs76018325 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028193 | CAGCTTTCCCATCTA[C/G]TAAGTGTCGGGTAGG | 114792 |
| rs76048574 | snp | C/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928341 | AAGAGGATGATGCTA[C/G]TGATACCTAATATTG | 114792 |
| rs76049071 | snp | A/C/T | 0.00398691 | 0.0444912 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921386 | TTTGAGTTACACTGG[A/C/T]GCTGGCTCCTGATGA | 114792 |
| rs76057354 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074293 | AACAAGTTTTGAGGG[A/G]TGCTGATGTCTGAAC | 114792 |
| rs76061775 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050270 | GCAGAAATAGAATGC[A/G]CAACCCCCCAACCCA | 114792 |
| rs76077125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028139 | GTGCTTCTCAAACAT[C/T]TATGTGCATGTGGTT | 114792 |
| rs76083021 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901377 | TTCTTCTAGAGACTT[C/G]CCGCATTTCTTGGCA | 114792 |
| rs76092111 | snp | A/T | 0.031825 | 0.122064 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947345 | TGCCCAATTCATGAA[A/T]TGTTCATTGCTCAAA | 114792 |
| rs76132178 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940728 | TTGCACACCAGACTT[C/T]GTAGTAAGATTCGTA | 114792 |
| rs76142004 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048772 | TGGACCATCCCTTCA[A/G]GGGTAGAAGTATCCA | 114792 |
| rs76144667 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112161 | TGGGGACCCATCTTC[G/T]TCTGCCCAGAATTTC | 114792 |
| rs76175597 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116869 | TGTGAAAGGAAATAC[A/G]TTTTCTTTGTTCTTC | 114792 |
| rs76218411 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977490 | TTCAATGTTTTTTCA[A/G]TTAACAAGTGACTAA | 114792 |
| rs76254037 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095060 | AATTTGTAATTCTAC[A/G]TGAATTACAATGTAA | 114792 |
| rs76293175 | snp | G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069416 | TTTTTTTTTTTTTTT[G/T]TGTACCAATGGCAAT | 114792 |
| rs76320550 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125289 | ATCCATTAGTTTTGA[C/T]TGATTATTCCAGCTC | 114792 |
| rs76338259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971576 | GGCTGATCAAATGGT[A/T]GCTCCCTGGCATTAC | 114792 |
| rs76346225 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991688 | ATCACTGCGTTCCTT[A/C]CCAAGCCGGAGAGCC | 114792 |
| rs76351889 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060523 | CCCACGTCATCATGC[C/T]CTATACAGAATCTCA | 114792 |
| rs76397330 | snp | C/T | 0.0138799 | 0.0821421 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141712 | TAATGTGAATTTCTA[C/T]AGGAAGGTCATGAGA | 114792 |
| rs76404500 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072835 | AATCTTCTGGGAGGC[C/T]ATATTGTTTGTGTTA | 114792 |
| rs76414100 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090491 | TGAATTAATCATTTT[C/T]TTCAAAAGGAGTCCC | 114792 |
| rs76421537 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059749 | TTTCATGTTCCATCT[A/G]TGAGAATTCTGTCAT | 114792 |
| rs76445973 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100801 | TTGGCTCATTATTCT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs76449307 | snp | A/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932204 | TAGAACTGACTGGGT[A/T]ATTTTTTTTTTTTTT | 114792 |
| rs76456357 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060977 | GCCTGCTACAAATTG[C/T]AGGAGATGTTCCTGG | 114792 |
| rs76475061 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033645 | TTACATTACAACCAA[A/C]AATAAACAAGGATTC | 114792 |
| rs76477192 | snp | G/T | 0.0399052 | 0.1355 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973719 | AGATTTTTGAGATCT[G/T]TACAGATTGCCTTTT | 114792 |
| rs76477593 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016609 | CTCAAAAGTCCAGTT[A/C]CAAAGTCTCATCTGA | 114792 |
| rs76479719 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121456 | TCTCAGGGGTGAGAA[G/T]AGACACATAATGTCT | 114792 |
| rs76513583 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065277 | GGGAGAGAAAACCCC[C/T]GAACACCAAGCACTG | 114792 |
| rs76514170 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006264 | CCATTAGGTAATGCT[A/C]TTCTTTGTCTTTTTA | 114792 |
| rs76523987 | snp | C/G | 0.0501905 | 0.150254 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009469 | ACTGGCCATGCTGTT[C/G]CTTCTGTTTTAATTT | 114792 |
| rs76557323 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089926 | ATGTGAGTGGCGTCA[A/G]ACAAGGTAAGACCTC | 114792 |
| rs76573989 | snp | A/G | 0.127599 | 0.217986 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014008 | GGAAATTTTCTCTCT[A/G]TATATGTTTCTTTTT | 114792 |
| rs76602230 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096394 | TCCCACCATTGGCTC[A/G]TTGGTCTCAGCATTA | 114792 |
| rs76605847 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029565 | AATTAAAACAATTGT[A/G]AAGAGGAAAGAAAAC | 114792 |
| rs76625113 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967399 | TAAAAAAGGAATCAA[A/T]AAACTATACATATAT | 114792 |
| rs76631508 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028160 | GCATGTGGTTCACCT[A/G]GGGCTTTCGTTAAAA | 114792 |
| rs76643609 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016191 | TCTGAAGGATGGTGG[C/T]CCTCTTCTCATAGCT | 114792 |
| rs76657473 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965137 | TCGTTTTGCATAATG[C/G]CCTGCAGTTGCATCC | 114792 |
| rs76665843 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942911 | TGTGTAGCAACCTGT[G/T]CACCTCTCTCTTGCC | 114792 |
| rs76687751 | snp | A/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016584 | ATAGGTGAAAGGGAC[A/T]TTCTTTGTCTCAGAT | 114792 |
| rs76697681 | snp | C/T | 0.139564 | 0.224285 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025687 | CTTGAGAGGGAGGCA[C/T]CTGAGTAGGCACAGA | 114792 |
| rs76725654 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965133 | TAATTCGTTTTGCAT[A/C]ATGGCCTGCAGTTGC | 114792 |
| rs76753491 | snp | G/T | 0.0652144 | 0.168387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050536 | AAACCTTTGCTCAGA[G/T]GTAAGGCAAGCAGGA | 114792 |
| rs76756676 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029901 | ATGGCCATTGTAAAC[A/G]TCATTAATTATGTAA | 114792 |
| rs76762587 | in-del | -/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922516 | ACTTTAAAAAAAAAA[-/AA]TCTTCTTCAGCTCAT | 114792 |
| rs76808115 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928377 | CTTACTGTAGCTGAG[C/T]GAGTGATGAAAGCTG | 114792 |
| rs76849888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046207 | CTAGGCACTTTATGC[A/G]TGCTGTTTAAACTAA | 114792 |
| rs76852771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986852 | CGCCCTGCTTCAGCT[C/T]ATGCTTGGTGCACTG | 114792 |
| rs76860331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091537 | TGATGTGGGGCTTTC[C/T]GCTTGCTGCTCTTTC | 114792 |
| rs76867580 | snp | G/T | 0.0603597 | 0.1629 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035607 | GTTTTGCCAGATATT[G/T]TATACTTGGCAGTTT | 114792 |
| rs76878278 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108439 | CCCAATGATAAATCA[C/G]CTTTCCTCTTACTGT | 114792 |
| rs76892984 | snp | A/C | 0.00574071 | 0.0532672 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976228 | ATAAAGAGAGGATGA[A/C]AATGTTTCCCAAACT | 114792 |
| rs76893605 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943448 | CCCACACACAGGCTG[A/G]CACCTGTTTTACTTA | 114792 |
| rs76933782 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026627 | CAAGATCGAAGGGAG[A/G]GTCCACACCTGGACT | 114792 |
| rs76963554 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931746 | AAGAATATGGTAAAA[A/T]ATGTTTTGTAATGGA | 114792 |
| rs76966010 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913335 | CCAGACTAACTGCAA[C/T]AACCAATCACTGTCT | 114792 |
| rs76978979 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917966 | ATTGTAGGATGTTTA[A/G]CAGCTTCCCTGGATT | 114792 |
| rs76984995 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108189 | CTTGCTGGCTTGGCC[A/G]CCAAAAATGCTGCAT | 114792 |
| rs76996219 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969387 | ACTTTCTACCAACCC[A/G]TCCAGTCTTTCCTTT | 114792 |
| rs77129837 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058742 | TGCTTTGAATGTAGA[C/T]ATAATGCCTGGTGGT | 114792 |
| rs77132151 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101509 | GGACACTTAAGAAAA[A/C]GAGAAGTGTTTGTAA | 114792 |
| rs77134787 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917018 | CAAAAACATAACAAC[A/C]ACCTTAGGAGAACCC | 114792 |
| rs77183832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063830 | TAGAATGGAGGGCTG[A/G]GGCATCACTAAAGGC | 114792 |
| rs77192473 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116588 | AAATATTTTAATAAA[C/T]ATTCCTTGTGTTTTG | 114792 |
| rs77209856 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045521 | AGTAAATAATATCTG[C/T]ACTCAGCTGCATTAG | 114792 |
| rs77224390 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026618 | AATAAAATGCAAGAT[C/T]GAAGGGAGGGTCCAC | 114792 |
| rs77233533 | snp | A/G | 0.0785177 | 0.181917 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006946 | TCATATCTACCTTAT[A/G]GAATCTGAGGACTAT | 114792 |
| rs77250659 | snp | C/T | 0.252983 | 0.249982 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978593 | TATTGTGAATAGCGC[C/T]ACAGTGAACATACAC | 114792 |
| rs77254729 | snp | A/C | 0.0165026 | 0.089325 | missense, intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113808 | GGTGGTTGGAACACA[A/C]CTGCCACTACCAGTA | 114792 |
| rs77260022 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966924 | ATTCAGAAACTTTAG[A/C]ATCAGGAAGACCCAG | 114792 |
| rs77261502 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913366 | TTGAAACGTAATGTA[A/G]GTCCCAGCTTGACTA | 114792 |
| rs77278215 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096634 | TATTCTTTTTGATAT[C/T]CACATTGGATTGGTG | 114792 |
| rs77291845 | snp | A/G | 0.127599 | 0.217986 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013097 | TACTTACCCCTCCTA[A/G]CCTTTACATAAGTGA | 114792 |
| rs77303603 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949393 | TCACACTTGTTATCA[C/T]TGTTCATTTACCCAG | 114792 |
| rs77332357 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958677 | TTGATCATCATGTAT[A/C]CAGTTATCTTGGCTA | 114792 |
| rs77370961 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013964 | GTCTCTGAAGTAGGG[A/G]TTTGTGCACCCCTGA | 114792 |
| rs77379631 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956749 | TTTAATTCTTATAAT[A/G]TTCGATTGTTGTAAG | 114792 |
| rs77433370 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024413 | TTGCTTTTTTTTTTT[C/T]TCAAATTAAATGACT | 114792 |
| rs77462006 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995983 | AAGTGAGGAAGTATT[A/G]AAACAGAGATAGCAA | 114792 |
| rs77473237 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076332 | TAAGTACTGTTAACA[A/G]CATTTGTAAAAGGGA | 114792 |
| rs77476104 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969084 | TTGGCTTGCAGTCTT[C/T]CTCCTCATCACAAAC | 114792 |
| rs77491580 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965135 | ATTCGTTTTGCATAA[A/T]GGCCTGCAGTTGCAT | 114792 |
| rs77501070 | snp | C/G | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059043 | TCCCAAGTTGATTCT[C/G]TCAGCAAGTGTAGGA | 114792 |
| rs77508215 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124049 | AAGCCCTGCAAATGA[C/G]TAACACTGCTAAAGA | 114792 |
| rs77508448 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107735 | CCTTATAAGAAAGCC[A/G]TAAAGATGAGATAAT | 114792 |
| rs77514841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933166 | CACCCCAACATAACG[C/T]CTTTGAAAACAACGA | 114792 |
| rs77529763 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031353 | AACATTTTTTTTTTT[G/T]GAGATAGAGTCTCAC | 114792 |
| rs77556005 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094322 | AGAATTATTTACATT[C/G]TAAGGAGATGTCAAG | 114792 |
| rs77560221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925195 | ACTACTCAGGTTACT[C/T]ATGCTGCCAGCCCTG | 114792 |
| rs77584332 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078357 | TCTATAGTAAAGTAT[C/T]GACATGGGGTAATTT | 114792 |
| rs77638888 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068151 | TTGATGAAGATGTCT[C/T]TTTTTTGCCGTTACC | 114792 |
| rs77645773 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097131 | AGGGAAAAAAACCAC[A/G]CAAATTTAAGAGTAA | 114792 |
| rs77650929 | snp | A/C | 0.10237 | 0.201756 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106345 | TACTCTGTAGAGTAG[A/C]AATCAGTAGGGATAT | 114792 |
| rs77659395 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106145 | CTGAGTGTGTTTCAC[A/G]TGAACAATAAAGGAA | 114792 |
| rs77695364 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946181 | TATTTAGGAAAAAAA[A/T]ATTTTAAATATTTTG | 114792 |
| rs77699016 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060469 | CCAGCTCCACCCTCC[C/T]AGAGCCCCCATGTGA | 114792 |
| rs77705171 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129299 | CATCGTATGACTTTT[C/T]TTCTGGCCGAAATCC | 114792 |
| rs77760723 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097548 | CACTCTGGAAATCAC[A/G]TTTTATTTTTTCCTT | 114792 |
| rs77764422 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941100 | ATTATTTCTTCCTTT[A/G]TACTTTTGTAAATAA | 114792 |
| rs77784311 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921691 | GCAGCTATCAGGAAT[C/T]GAACAAAGAACTATG | 114792 |
| rs77787846 | in-del | -/G | 0.0991586 | 0.199366 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099474 | TCATTCGACATTGAT[-/G]GTTCTCAGTGAGGCT | 114792 |
| rs77821527 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927409 | AAGTGGGAACTCAGA[G/T]ACATTAAATCCCAGC | 114792 |
| rs77864213 | snp | G/T | 0.194278 | 0.243711 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063946 | TGGCAGCAGTAGGTA[G/T]ATAATTGGACTTAAC | 114792 |
| rs77866614 | snp | A/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982202 | GTCTCTTTGTAGGTC[A/T]CTAAGGACTTGCTTT | 114792 |
| rs77873101 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094125 | ATAAATTTCTTGAAA[C/T]TGATAAATGTTAGTC | 114792 |
| rs77903999 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018776 | TTCTATGCTGGCCAA[A/G]GTAACAATCTATCAG | 114792 |
| rs77908948 | in-del | -/CTAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055795 | AGACTGAGAACCTGT[-/CTAA]AAAAAAAAAAAAAAA | 114792 |
| rs77956221 | snp | A/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060223 | ATGCCAACTCACTTG[A/T]TCACAGGCAGGAGAA | 114792 |
| rs77982175 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915072 | AGAAAGAATAAATGT[C/T]ACTTGTGCCTCCTGA | 114792 |
| rs77992706 | snp | A/G | 0.202035 | 0.245356 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050796 | TCACCTGTGGTCAGG[A/G]GTTTGAGACCAGCCT | 114792 |
| rs78003453 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904356 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAAG | 114792 |
| rs78020362 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111193 | CATGAAGGGAAACAG[A/T]GCCAACATTCCTTTC | 114792 |
| rs78025755 | snp | C/T | 0.0263992 | 0.111815 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139728 | AAATTTAACATTATG[C/T]AGCCCTGCTCAGTAG | 114792 |
| rs78034987 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939252 | CATTGCCAGTTTTCT[C/T]AGTAATACTGTTTTA | 114792 |
| rs78042097 | snp | C/G | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901468 | TTTCCATCGTAACAC[C/G]CTTATGATTACATTG | 114792 |
| rs78043902 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920454 | GTGACACACAGCATC[A/G]ATGGTACTGAGGTGA | 114792 |
| rs78063418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965154 | CTGCAGTTGCATCCA[C/T]ATTGCTGCAAAGGAC | 114792 |
| rs78080606 | snp | C/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896197 | TCACTATATACAAAG[C/G]ACTTGTGCCCAGGAC | 114792 |
| rs78082161 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917653 | GGCCTCCTCTGGTAT[G/T]CAGGCATGTTTGGGT | 114792 |
| rs78092474 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071710 | TACACTCTGCCAAGA[A/C]CTCATGAATTCCACT | 114792 |
| rs78094583 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026764 | TTAAAATTTTAAGAG[C/T]GATCATTAGTTTACA | 114792 |
| rs78140037 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049575 | AGAAAGCGAAACCGT[C/T]GATAACGGGGGGCGG | 114792 |
| rs78148679 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038077 | AATAACTAGAAGACA[A/G]TATTGGGGAAATGCT | 114792 |
| rs78233059 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060887 | GGTCGGTTCTTATCC[A/C]CACCAAAATGAGTGT | 114792 |
| rs78233888 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104744 | TTATAGCACTCAGGT[A/G]AGCACTGTTATAATT | 114792 |
| rs78251553 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901341 | GCCTTTTTTTTTTTT[-/TT]ACTTTAAATGGGGAA | 114792 |
| rs78301355 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933234 | CCTTACCCCTCAAAA[C/T]ACGTGCCTTGATTAC | 114792 |
| rs78303912 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046499 | TAAACTTGGAAACTG[G/T]GCCTTTTCAAGTCAG | 114792 |
| rs78322689 | snp | A/T | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142287 | ACAAATGCAATGAAT[A/T]GGATAGCCATTGGCA | 114792 |
| rs78355936 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048021 | CACTATATGCCAAGC[A/T]CTGTGATAAATACCT | 114792 |
| rs78380220 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938075 | TCAAGTAATGAATAA[C/T]TTAAAACAAACAAAC | 114792 |
| rs78413225 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059039 | GTTCTCCCAAGTTGA[C/T]TCTGTCAGCAAGTGT | 114792 |
| rs78441442 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129534 | CTTCCCATTACTGAG[A/G]GTGAACAGGAACCAA | 114792 |
| rs78481175 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063677 | TTGTTAAAAACACTA[A/G]TTGCCTCACCCTGAA | 114792 |
| rs78519500 | snp | C/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909346 | TTTGCATGTGTGTCA[C/G]GAAGGCTTATTTTTG | 114792 |
| rs78523985 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932220 | ATTTTTTTTTTTTTT[G/T]TGAGATTTCAAAGCC | 114792 |
| rs78527003 | snp | A/C | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039089 | AGCAAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 114792 |
| rs78539531 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106742 | GAGGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAT | 114792 |
| rs78567928 | snp | A/G | 0.00320089 | 0.0398773 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896800 | CTTTTAGAAACGACA[A/G]CAGCTTTTCATCTTT | 114792 |
| rs78568658 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079529 | TCTGGGGAATAACCA[C/T]TGAAGGAACCAATTA | 114792 |
| rs78584406 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105052 | ATTGCATGGCAAATC[A/G]CAACACCTGCTCACT | 114792 |
| rs78585536 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128681 | CTGCCAACAGGCAGG[A/C]TGGGGTGACCTCTGC | 114792 |
| rs78620064 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916143 | GAGACATACAGGAAT[C/T]GAAAGTGAGGTACAG | 114792 |
| rs78665952 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048047 | TACCTTACATGTAGT[A/G]GAGGAAGGGTTGAAA | 114792 |
| rs78685873 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938236 | TCTCTGGCCACCAGA[A/G]TAGTGAAGTTATAGT | 114792 |
| rs78729677 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037288 | TGAAAACATAAAACT[C/T]TCTAATGCAGTGAGA | 114792 |
| rs78739695 | snp | G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911849 | TTTTTTTTTTTTTTT[G/T]TTGGCAGCTGCCACT | 114792 |
| rs78741423 | snp | A/C | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105766 | TTTGTAGACCAAGAC[A/C]AAAAAAAAATACTTG | 114792 |
| rs78775575 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114992 | GTGCATTGAGAGAAG[A/G]GATTTAAGTTACCAA | 114792 |
| rs78838555 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017729 | ACTTTCCAGTCCCAC[A/T]TGTATCTAGGTGGGG | 114792 |
| rs78847741 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958043 | AGCAAGATAGATGTG[A/G]ATCCTGCCCATATAG | 114792 |
| rs78859436 | snp | A/T | 0.0501905 | 0.150254 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029204 | ATTCAAGAGGAGGAG[A/T]ATTCTAAACAGACAG | 114792 |
| rs78863391 | snp | A/G | 0.202343 | 0.245416 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052263 | GCAGATGCACATGCA[A/G]ATGCAGACTGGTGAA | 114792 |
| rs78866194 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075644 | TTCCAAAGGCCAGAC[C/T]TTACCGCACATCCAC | 114792 |
| rs78903711 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079870 | ACCTTTTTAGAAAAA[A/G]AAAAGAGTAAGATTT | 114792 |
| rs78911082 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937565 | GTCCCCCTCAGGGAG[A/T]TGAGCTGACTCCTCA | 114792 |
| rs78926189 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123028 | GTTCTTTGCATCCCA[C/T]TCTGTCCTGGTAGTG | 114792 |
| rs78941665 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965134 | AATTCGTTTTGCATA[A/T]TGGCCTGCAGTTGCA | 114792 |
| rs78962110 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136411 | AACAAGAGAAAAGCA[C/G]AGATACTCTTAGGTT | 114792 |
| rs78973326 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036442 | TCATGTTCCTTGTAG[C/T]CTTGCATTGGTGTCT | 114792 |
| rs78985191 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916361 | AAGGGCTCAAATATA[C/G]AAGTACAGTCTTTCT | 114792 |
| rs79054094 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915849 | TAAAAGCAGAAAACA[C/T]AGAAAAAGCTCTTTG | 114792 |
| rs79124302 | snp | A/T | 0.0693013 | 0.172766 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078941 | CGGTAGCCAAAACTA[A/T]GACTATGTTTCAGAA | 114792 |
| rs79159123 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007449 | TTGAATATGGATGAT[C/T]TTTGTTCCTATCCAT | 114792 |
| rs79163645 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993022 | TCAGATGGAGAAAGC[C/T]GAATAAAGTTGGAGC | 114792 |
| rs79205754 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936750 | CCTAAAACTGCAGCA[C/G]CTTCCATCCCAAGAA | 114792 |
| rs79229319 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969900 | CTTAAAGACAACTCA[A/G]ACTTAACATGTCCCA | 114792 |
| rs79229721 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942330 | ATGCCCAACATGCTT[A/C]TTCACCTCAATCTCA | 114792 |
| rs79238471 | snp | C/T | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009650 | CTGTTTTGAACATAA[C/T]TTGTTTACTACTTTG | 114792 |
| rs79239014 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953903 | ATCAACAATTCAATC[C/T]TCAAACTCTCCTCTA | 114792 |
| rs79241754 | snp | C/T | 0.0015647 | 0.0279267 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085246 | GAACTCCTGAAGAGC[C/T]GCCCAGAAGAAGTTC | 114792 |
| rs79254111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120094 | ACGCTGAGAGCATTT[C/T]CCAGGTACCAGGAAC | 114792 |
| rs79264342 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067704 | GAGAAACTTAAATTC[A/G]GAACTAGGATGTTGA | 114792 |
| rs79284810 | snp | C/G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975223 | AAGGGGTAAGTTTCA[C/G/T]AATGTGTGAGGTTAG | 114792 |
| rs79286874 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957324 | AAATTAATCACTGGA[A/G]AATGGTCATTTGCTA | 114792 |
| rs79292545 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091995 | TCTTTTTTTTTTTTT[G/T]TTGTTGTTGTTGAGA | 114792 |
| rs79295179 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991240 | GGAGCCCCTCCCAGG[A/G]AAACTTAGAGCCACT | 114792 |
| rs79315616 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914921 | CACTACAGCCCAGAA[C/T]CCCTGGGCTGAAGCC | 114792 |
| rs79318618 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069029 | AAGGGAAACAGAGAA[A/G]GGGGGGGTCTGTTGC | 114792 |
| rs79321639 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106743 | AGGAGACCCTGTCTC[A/C]AAAAAAAAAAAAATT | 114792 |
| rs79365891 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989795 | TGGAGGATTTACTCA[G/T]TTTTTAAACTTTTGG | 114792 |
| rs79390994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090080 | TGTTCATATTTGTCC[A/G]TGATTATCCATCCCT | 114792 |
| rs79420372 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109589 | TTAGTTGAGGCTTGT[A/G]TGCTTCTCACGCAGT | 114792 |
| rs79497083 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033816 | CTGTTGCCCATTTGT[A/G]TGCCTTCTTTGGAAA | 114792 |
| rs79509055 | snp | A/G | 0.144296 | 0.226554 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019684 | TATTTAAAAATAGGA[A/G]ACATCCAAAATAAGA | 114792 |
| rs79528481 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060919 | GAGTTTCAGCATTTG[A/G]AATGGGAATCAGTCG | 114792 |
| rs79543670 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069899 | TAATTAAGTAATACT[A/T]CAATGACTTATAGGA | 114792 |
| rs79576855 | snp | C/G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911853 | TTTTTTTTTTTTTTG[C/G/T]CAGCTGCCACTCCTC | 114792 |
| rs79584682 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118170 | ATTTATATGAAGTTT[A/G]CATTGCCCCATTTTA | 114792 |
| rs79605741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001132 | ACATTTATAAAAACC[C/T]ATAGAATATACAACA | 114792 |
| rs79606489 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016688 | ATTGTGTTTTGAATT[C/G]TGAGGACATGCGGTT | 114792 |
| rs79629374 | snp | C/T | 0.030665 | 0.119967 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896205 | TACAAAGCACTTGTG[C/T]CCAGGACTTACATAA | 114792 |
| rs79636108 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054311 | TATACTTCATAAAAA[A/C]CATCCATTTACATTT | 114792 |
| rs79637443 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942910 | ATGTGTAGCAACCTG[G/T]TCACCTCTCTCTTGC | 114792 |
| rs79653936 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032605 | TCTGCAGTTTAAGCT[A/G]TTTTGAGTCCTGCTG | 114792 |
| rs79687390 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951593 | CATCATCATCAAGAC[A/G]ATATTAATTGCTCAC | 114792 |
| rs79773276 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142364 | GTAATTTACAATGCA[A/G]GTTATCACAGTATCA | 114792 |
| rs79844080 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053385 | TCCCAGCTTGCTCCA[C/T]AAATAAATCATTCCA | 114792 |
| rs79869996 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118932 | TGACTATTGCAGAAG[G/T]CAGGAAAGGTAGCAC | 114792 |
| rs79877671 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033246 | GAAACTAAACCCACC[A/G]TATGCCTATATAAGT | 114792 |
| rs79878366 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093520 | CTCAAAGTACCTTAT[A/G]TATCTCATAAGTCAA | 114792 |
| rs79894414 | snp | A/C | 0.213937 | 0.247385 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026339 | ATCATGTCACTGTAC[A/C]CTAGCCTGGGTGACA | 114792 |
| rs79924668 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920865 | TCCTTTCACATAAGT[C/G]TTTGAACTTTTGTTT | 114792 |
| rs79945520 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084157 | TTATAGAGTGAAATG[G/T]ATATCTGATAGCATT | 114792 |
| rs79946097 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970415 | TCCTGCCACAGGATC[A/G]TAGCATTTGCTGTTC | 114792 |
| rs80031134 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058521 | TTTCTTTATATAGAA[C/T]TCTAATTTGATTTGG | 114792 |
| rs80046016 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099475 | CATTCGACATTGATG[G/T]TTCTCAGTGAGGCTG | 114792 |
| rs80051201 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066507 | TACATGCTTGTGGAC[C/T]GTTATTATTCAGGCT | 114792 |
| rs80073866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963505 | GTGTTTAGAGCTACT[C/T]CTGCATCTGCTGGTT | 114792 |
| rs80075790 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047926 | GAGTACCTTAGGACC[A/G]AAATGGAAGCAAATA | 114792 |
| rs80090353 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014443 | ATATGTAAATATTAG[A/G]GCTACTACTCAACAG | 114792 |
| rs80092522 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096385 | TCATAATACTCCCAC[C/G]ATTGGCTCGTTGGTC | 114792 |
| rs80093337 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116303 | TTCTTTAAATGTATA[C/T]TTCAACAGTTAATAA | 114792 |
| rs80097008 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973732 | CTTTACAGATTGCCT[C/T]TTTTTTTTTAGACAG | 114792 |
| rs80099923 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079562 | GAAAGAGGCCACACA[C/G]AAAGACTGAGTTTGG | 114792 |
| rs80108354 | snp | A/C | 0.211516 | 0.24702 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014307 | CTCAAAAAAAAAAAA[A/C]AAAGTTTCTTTTTTC | 114792 |
| rs80136860 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996002 | CAGAGATAGCAAGAG[A/C]AATGAGGGGCCTCGA | 114792 |
| rs80141128 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097634 | GCAGCTTTCTCTGCC[C/T]TTTTTTTTTCTTTTT | 114792 |
| rs80199383 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069018 | TTTATCATTGTAAGG[A/G]AAACAGAGAAGGGGG | 114792 |
| rs80216382 | snp | C/G | 0.201418 | 0.245234 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023585 | ATCCAGGGCAACAAG[C/G]ATTGTACCCATTCCT | 114792 |
| rs80216687 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055273 | GAAACAGAAAGGAAG[A/T]TCTTCATCATCTTAC | 114792 |
| rs80247659 | snp | A/G | 0.202035 | 0.245356 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051860 | TATTGAGAAAAAAAG[A/G]ACAATTGTGCTCCAG | 114792 |
| rs80252902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063834 | ATGGAGGGCTGGGGC[A/G]TCACTAAAGGCCTCC | 114792 |
| rs80255600 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930566 | CCTCTGCCTCCCCTT[C/T]CCCCACTCCTTTGCC | 114792 |
| rs80266067 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049595 | ACGGGGGGCGGGGGG[C/G]AACTACTTTATTTTG | 114792 |
| rs80266393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007662 | GGATGAGGTTTTTTG[A/C]TTTTTCATCTTTGAT | 114792 |
| rs80278796 | snp | A/G | 0.031825 | 0.122064 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053104 | CACACACACACACAC[A/G]CACACACATTCTCTC | 114792 |
| rs80329988 | in-del | -/GAG | 0.337571 | 0.234161 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018151 | AATTAATATTGAATC[-/GAG]GAAACTTTTTTCAAT | 114792 |
| rs80350749 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918965 | CCTTTCCCTTATGGA[G/T]GTAAGAGAACTTCAC | 114792 |
| rs111233770 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066658 | TTGACTATATGAGTA[C/T]CAAAATCATGTCGAC | 114792 |
| rs111239646 | in-del | -/AAGC | 0.409041 | 0.192888 | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010244 | TGATAGAAGCAATGG[-/AAGC]ATCAGCAGAATGGGT | 114792 |
| rs111261091 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983983 | TGTTAGGGTGTCAAT[G/T]TTAGATCTCTCCTGC | 114792 |
| rs111265494 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986034 | TTTGATGATGGTGAC[A/G]TACAGATGGGGTTTT | 114792 |
| rs111270210 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978309 | CAACCTCCACCATTA[A/G]GTAGGCCCCAGTGTC | 114792 |
| rs111273844 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111416 | GAATGCGGGTGCTGG[A/G]GCTAGCCAGCCGCTT | 114792 |
| rs111277963 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961834 | GCTCTCTGATATCAA[A/G]AAGGTCCCTCTTCAG | 114792 |
| rs111287491 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132796 | AAGTGGTTCAGCGAG[A/G]TTACATTTTGCAATG | 114792 |
| rs111320900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091413 | TGAGTGCCTGCTCTA[C/T]CCAGCCATGTCCTGT | 114792 |
| rs111336646 | in-del | -/G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112031 | TTATGGGTACAGGAT[-/G/T]GGGGGGGTGGGGTGG | 114792 |
| rs111340361 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116651 | GTTTCCCTTACATAG[A/T]CTTAAAGATATGACG | 114792 |
| rs111341807 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088926 | TTAGGTTCTCTTTCA[C/G]CAGAGTAAGAGGGAG | 114792 |
| rs111359407 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986966 | CTTCTGCATCGCTCA[C/T]GCTGGGAGCTGTAGA | 114792 |
| rs111361190 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003591 | TCTGAAATGGTATTT[C/T]CTAGATTATCTTCCA | 114792 |
| rs111422573 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97134513 | TTTTCAGAATTGGTA[A/G]AACTCAGAACTGGGC | 114792 |
| rs111447891 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071428 | CTTCCATTAGCTCCT[C/T]GACTGTCCCTCAAAG | 114792 |
| rs111448419 | snp | A/G | 0.128288 | 0.218372 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112533 | CTCACTGTAAGCTCC[A/G]CCTCCCGGGTTCAAG | 114792 |
| rs111454559 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029876 | TTAGTTCAAATCTCT[A/G]TAATGCCTCATGGCC | 114792 |
| rs111464623 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916512 | TACTGTCTCTTGAAG[C/G]TCAAACCTATTTTCC | 114792 |
| rs111480571 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986611 | TGCTGCCTTGCAGTT[G/T]GATCTCCCACTGCTG | 114792 |
| rs111481699 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960889 | ATTGTCTAAAGACCT[A/G]GAATCAACAGAAAGG | 114792 |
| rs111507285 | in-del | -/T | 0.0345262 | 0.126772 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132972 | GATGAATTTTGAAAA[-/T]ATATATGTAATATAT | 114792 |
| rs111509595 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063133 | AGTCTGGTTGATATT[A/G]TTAAAACAGATAGTG | 114792 |
| rs111516581 | in-del | -/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027571 | TCAACCAAAATAATT[-/G]GGGGGAAAAGGGAGA | 114792 |
| rs111520164 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116574 | TATGAATTTCTCATA[A/G]ATATTTTAATAAATA | 114792 |
| rs111529154 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065368 | ATCTAAAACATCAGA[A/G]ACTCAAAATATATCC | 114792 |
| rs111530082 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074528 | CAAATCTGAAACAAA[C/T]AAACAAAAAAACCTT | 114792 |
| rs111532691 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072254 | CTACTACTGTCTTCA[A/T]TCAGATCCACATTAC | 114792 |
| rs111533906 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953630 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAGAAA | 114792 |
| rs111536217 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982975 | GTTTTCAAGGGAATG[C/T]TTCCAGTTTTTGCCC | 114792 |
| rs111539573 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099943 | AAAAATATTATTTGT[A/G]TGATCAGCTTGGCCA | 114792 |
| rs111560971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077573 | CTGGCACCACAAGAG[A/G]GCATTCCATTTTATT | 114792 |
| rs111569019 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983291 | GATTGCCAGTATTTT[A/G]TTGAGGATTTTTGAA | 114792 |
| rs111579218 | in-del | -/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934459 | ACTTAACAACAACAA[-/C]AAAAAAATAGCAAGT | 114792 |
| rs111580800 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931457 | TAGGATCCCATAGAC[A/T]GAGCTAAGCTTTGTT | 114792 |
| rs111594320 | in-del | -/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084986 | TATAATTGTGATTTC[-/T]TTTTTTTTTTTATAC | 114792 |
| rs111594342 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036555 | ACCTGAGGTGTGATG[A/T]TGGGTGGGGTGTGTG | 114792 |
| rs111600964 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071758 | CCATTTAAATCTTTC[C/T]CAGATATGCTACCTT | 114792 |
| rs111612212 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982229 | GTTTATTAATCTGAG[C/T]GCTCCTGTGTTGCGT | 114792 |
| rs111621076 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962043 | TTTTCGGTCATATAA[C/T]TTGCCAGTGGCAGTT | 114792 |
| rs111621181 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986069 | TGGATGTCTTTTCTG[C/T]TTGTTAGTTTTCCTT | 114792 |
| rs111625754 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951905 | TGTTTTGTTCAATGC[C/G]ATTTCATTACAAGGT | 114792 |
| rs111632864 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118195 | ATTTTAAATAACTTC[A/G]ATTTATTCAAAGCTA | 114792 |
| rs111653706 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966525 | CTACTTTTCAGAAAT[A/C]TGCTCTTGAATGGAA | 114792 |
| rs111655574 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093504 | TTTAAGAAAACAGAA[A/C]CTCAAAGTACCTTAT | 114792 |
| rs111656932 | snp | A/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97008053 | TGGCATTCCTGCTGC[A/T]CCTCCTCATGCAGGT | 114792 |
| rs111664041 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120673 | GAAAAGTGTGTGTTG[C/T]GGGAGTAAGTAGTAA | 114792 |
| rs111674476 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073216 | CAAATTGACAACCTA[C/T]TGGACAAATCTGTTC | 114792 |
| rs111701676 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072007 | TCTATAATGTACCCT[A/T]TTCTGACTGTACCCC | 114792 |
| rs111706029 | snp | A/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989958 | GTTTGTTTCTTTCTT[A/T]TAATGGCCATTTCAT | 114792 |
| rs111710878 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138898 | AATGCTTATAAATAT[A/G]CATGTATGTATATAT | 114792 |
| rs111724631 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980901 | TTGACTCACAGTTCT[A/G]CAGGGCTGGGGAGAC | 114792 |
| rs111770851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960930 | TTAAGGTAAGGGGTT[G/T]TGGAGACCAATGTTC | 114792 |
| rs111778864 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037169 | ATTGTATTTAAAATA[A/T]ATTTTAGAAAATTTC | 114792 |
| rs111779335 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041898 | GCAAGATAATGGATT[C/T]TCATTGTTATCACTG | 114792 |
| rs111781545 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058198 | CTCCAACTTTGTTCT[C/T]CTTCAACATCGTGTT | 114792 |
| rs111786462 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049571 | CCGTAGAAAGCGAAA[A/C]CGTCGATAACGGGGG | 114792 |
| rs111805687 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983963 | TCTAGTTCTTTTAAT[G/T]GTGATGTTAGGGTGT | 114792 |
| rs111811781 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072798 | TGGAATTATATCTTC[C/T]TCCTCTTCTTTAATT | 114792 |
| rs111812319 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975607 | TGGGAAGGGTCACAC[A/T]CACATATACACATGC | 114792 |
| rs111812913 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937010 | ACCCCTTCACTCTCA[A/G]TTCATCTTACCCTGT | 114792 |
| rs111815856 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111407 | CGGGAACTGGAATGC[A/G]GGTGCTGGGGCTAGC | 114792 |
| rs111832018 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043250 | TAGCCTTTGGTAACC[A/G]TCATTCTACTTGCTA | 114792 |
| rs111849323 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985879 | GTCTCAACTCGTCAA[A/C]GTCATTCTCCGTCCA | 114792 |
| rs111852276 | in-del | -/TTTA | 0.40386 | 0.197046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043451 | ACATACCATCTTTTC[-/TTTA]TTTATTCATCTGATG | 114792 |
| rs111855522 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139485 | CAACATTCAATATGT[A/G]TGACTTTTATTGTGG | 114792 |
| rs111876728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075756 | CTTGATTTATAACTC[A/G]GTTGTAATCAAAATA | 114792 |
| rs111879913 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062908 | GATGGTCAGGGAAGG[C/T]ATCTCAGGTAAGACG | 114792 |
| rs111883405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061472 | TGTGATATGCTCCTC[C/T]AGACTGATGAGTGAC | 114792 |
| rs111883716 | snp | A/G | 0.079617 | 0.182947 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091249 | AACAGAAAAAAGAGC[A/G]TGACCATTCTAGTTC | 114792 |
| rs111927332 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070209 | GAAAGTTAAAGTACA[A/G]AGTTTGGAAAACATA | 114792 |
| rs111928032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067647 | TTTCCACTGCTAAGT[C/T]ACCCCTTAACACTGG | 114792 |
| rs111931517 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931637 | GCATTTTTACTAGTT[A/G]GTAACATTACTTGAG | 114792 |
| rs111931786 | in-del | -/A | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968402 | AACAAAAACAAAAAC[-/A]AAAAAAAAAAACATC | 114792 |
| rs111944035 | snp | C/G | 0.0614824 | 0.164198 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042826 | GGATGTTTGTCCTCT[C/G]CAAATCTCATGTTGA | 114792 |
| rs111944999 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070416 | TTGGCTTTGAAATGC[A/G]TCATAAGATCTGCAG | 114792 |
| rs111966511 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972516 | GAGAAAGAGGTTGCA[C/T]TGGGGAAGCCAGGAC | 114792 |
| rs111970603 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986325 | TCAGGGGTCAGGGAC[C/T]CACTTGAGGAGGCAG | 114792 |
| rs111972356 | snp | C/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968235 | TTTGCCACCAGTGTA[C/G]GTTGTGCAATATCTG | 114792 |
| rs111972723 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108974 | TAAATACAGCTTCGT[A/C]GAGTAACTAAATTCA | 114792 |
| rs111973150 | snp | A/T | 0.10237 | 0.201756 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106477 | ACCGGGTGCAGTGGC[A/T]AACACTTGTAATCCC | 114792 |
| rs111975251 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982744 | TTGTATCCTGAGATG[C/T]TGCTGAAGTTGCTTA | 114792 |
| rs111996868 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032614 | TAAGCTATTTTGAGT[A/C]CTGCTGTATATACGG | 114792 |
| rs112047347 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921243 | TTTTTACAAAGCTCC[C/T]ATCATGTGACTAGTT | 114792 |
| rs112050623 | snp | C/T | 0.114738 | 0.210248 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978449 | GGCCTCCAGCTCCAT[C/T]CATGTTGCTGCAAAG | 114792 |
| rs112050672 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134872 | AATAAAAAAAACTTC[A/G]TAGTCGCATCATTTG | 114792 |
| rs112058637 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050532 | TTTTAAACCTTTGCT[C/T]AGATGTAAGGCAAGC | 114792 |
| rs112065697 | snp | A/C | 0.444444 | 0.157135 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007220 | ATTTATTTTTGTCTG[A/C]CTGAAATATTTTGGA | 114792 |
| rs112071718 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111430 | GGGCTAGCCAGCCGC[C/T]TCAGTGCCAGCAGAG | 114792 |
| rs112080075 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029198 | GGCCACATTCAAGAG[A/G]AGGAGAATTCTAAAC | 114792 |
| rs112081836 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909840 | ACACATTAAAAATTA[A/G]AAATAGAATGTCAGC | 114792 |
| rs112120534 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111661 | TTTGCCATCTGTGGA[C/T]GGCTTAAATATTAAC | 114792 |
| rs112122686 | in-del | -/C | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980179 | TCCTGATCACTCTGG[-/C]CTAGGACTTCCAGTA | 114792 |
| rs112131561 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982008 | GTGCCATGTGCATAT[A/G]ATAAAAATATATATT | 114792 |
| rs112131635 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961862 | CAGGCAGCTGTTGCA[A/G]GCCCAACCTGTGCAA | 114792 |
| rs112133279 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099181 | TTCCCTCATACACCT[A/G]CATGACATGACTGCC | 114792 |
| rs112139028 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107422 | AGTTAAAAACAGTTT[C/G]TAGTTCTAGCTTTTC | 114792 |
| rs112153814 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140294 | AAGCTAAAAAATAAT[G/T]TAGTTGTACTAATTA | 114792 |
| rs112168871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941634 | CTTCACGTAATCCAC[A/G]AAAGCCCCTCTTATG | 114792 |
| rs112172323 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010995 | ACACGTACACCTGCT[A/G]TACCTAACAGCCTGC | 114792 |
| rs112178972 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041733 | TAAGATTCACATCCT[A/C]TTAATTTTATGACTA | 114792 |
| rs112184709 | in-del | -/T | 0.143959 | 0.226396 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019791 | TTTTATACTATTTTC[-/T]CTTTTTTTGAGACGG | 114792 |
| rs112196746 | in-del | -/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932569 | TTGTCAATTTCCCCC[-/T]CCCCCCTTTTTTTTT | 114792 |
| rs112204375 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121854 | TAAAGCTACGCCATA[A/G]AAATAGGGAATGGCT | 114792 |
| rs112214717 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072628 | GTCATTATGAACTTT[A/G]TGCATTTCCCTGTAC | 114792 |
| rs112223220 | snp | C/G/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060826 | CTTGTGGGTTTTACA[C/G/T]TATTACTTTGTCACA | 114792 |
| rs112231507 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987421 | TGTGTCTTTGTTCTC[A/G]TTGGCAAACCACTGC | 114792 |
| rs112231754 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994971 | CCACACTACCTGGCA[A/C]ATAGTAGGCACTATT | 114792 |
| rs112260714 | snp | A/C/T | 0.0205665 | 0.0994132 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985517 | AGTATACCAATCAGA[A/C/T]GTAGATTTGGTCTTT | 114792 |
| rs112265962 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970458 | AACCTTCTCTTTCAC[C/T]TTTAAAAGATTAACT | 114792 |
| rs112286670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986749 | GGGTGGGAGTGACCC[A/G]ATTTTCCAGGTGCCA | 114792 |
| rs112309253 | snp | G/T | 0.0490535 | 0.14873 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987293 | TCTAGTTCTTTTAAT[G/T]GTGATGTTAGGGTGT | 114792 |
| rs112313353 | snp | A/G | 0.5 | 0 | synonymous-codon, intron-variant, missense, splice-acceptor-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113785 | CCCTCTGTTTCAGCT[A/G]GCTGTGAGGTGGTTG | 114792 |
| rs112333403 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072269 | ATCAGATCCACATTA[C/T]TTATTTTATGGACTA | 114792 |
| rs112359164 | snp | A/G | 0.213635 | 0.247341 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027119 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 114792 |
| rs112376012 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081425 | TTGCATATGAAAGCC[A/G]TTTGCTCTCTCAAAG | 114792 |
| rs112376472 | in-del | -/AG | 0.220246 | 0.248223 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993983 | CCCTTTGCTCTACAT[-/AG]AGATACTGTATCTTC | 114792 |
| rs112384004 | in-del | -/A | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956722 | CCTTTTTCTTCTGGG[-/A]AAAAAAGCTCATTTA | 114792 |
| rs112388358 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973889 | ACCATGCCTGGCTAA[C/T]TTTTGTATTTTTAGT | 114792 |
| rs112389449 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963753 | AATGTTCAGTAAAAT[C/T]AATAAATTCTCTGTT | 114792 |
| rs112408037 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962052 | ATATAACTTGCCAGT[G/T]GCAGTTTTAAGATCA | 114792 |
| rs112415398 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898183 | GTGGAGTGAGGCCCA[A/G]CATTGGATAAGACTC | 114792 |
| rs112419425 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112116 | TCTCACTTTGGGCTG[C/T]GGTGCCAGGCTTGAG | 114792 |
| rs112423266 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976468 | AGTGCTTCATGTGGG[G/T]GTGCAGACTGGAGTG | 114792 |
| rs112431010 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953449 | AGCTTGACCAACATG[A/G]CGAAACCCTGTTTGT | 114792 |
| rs112443045 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984054 | ACACTGCTTTGAATG[C/T]GTCCCAGAGATCCTG | 114792 |
| rs112448700 | snp | C/T | 0.215446 | 0.2476 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022467 | TACCTGTGATAACAC[C/T]TAATTTTTTTTTTTT | 114792 |
| rs112470596 | snp | C/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078942 | GGTAGCCAAAACTAA[C/G]ACTATGTTTCAGAAA | 114792 |
| rs112474323 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062595 | TTTCTTATAAAATTA[A/G]TTAAAATTGATTCTG | 114792 |
| rs112494712 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971747 | GTGGAAAAAAACAGA[A/G]GGACATATATCCCTG | 114792 |
| rs112511809 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933815 | CTCATGGTGGCTTGA[A/G]TCACAGATCAGTACT | 114792 |
| rs112525045 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933113 | CATGGAATTAGGACA[A/G]GATGAATTAGTTACA | 114792 |
| rs112560296 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089736 | AGCGAGTGGAGATTG[C/T]GCCACTACACTCCAG | 114792 |
| rs112563016 | snp | A/C | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135422 | GTCATTCTCCTGCCT[A/C]AGCCTCCTGAGTAAC | 114792 |
| rs112563122 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971612 | GGTCATCTTACTGTT[A/C]AGGGAGTCTGGGGCT | 114792 |
| rs112579353 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987683 | AAGCTGGAGGCATCA[C/T]GCTACCTGACTTCAA | 114792 |
| rs112617150 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986829 | ACTTCCTGGGTGAGA[C/T]GATGCCTCGCCCTGC | 114792 |
| rs112618827 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971702 | ACAGGCAGCCTGACG[C/G]GGGTTGCCTAAAGCC | 114792 |
| rs112640562 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019271 | ATTTGCGTTCCTTGG[A/G]AAGTAGACTCTGAGA | 114792 |
| rs112660434 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102263 | ATCAGGATTTCCCTG[A/G]CCATTTCAGCTGACT | 114792 |
| rs112661230 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134187 | AAAAAGTAATCTCAA[A/G]GAAAGTAGAAGAGGA | 114792 |
| rs112674536 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934074 | TTAAGTGCTTTGTTT[A/G]TATTAAGAGTGCTCT | 114792 |
| rs112677836 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069575 | AAATGTCTCACCACC[G/T]CCAGTTACACTGTGG | 114792 |
| rs112680732 | snp | A/G | 0.00941256 | 0.0679535 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114010 | CAGGACCAAACCACG[A/G]TTCCAGTCAGACACT | 114792 |
| rs112698391 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985305 | TGGCTGCCCTTATCA[G/T]TTTTTCCTTCATTTC | 114792 |
| rs112701919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934107 | TACTGCTTTTGACTG[A/G]GCATTGTAGGACCTT | 114792 |
| rs112705931 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004508 | GCTAGGACTTCCAGT[A/G]CTGTGTTGAATAGGA | 114792 |
| rs112722560 | snp | C/T | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897738 | GCTTCATCTTGCTGA[C/T]TTCCCGTTCCGCTCG | 114792 |
| rs112724806 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904194 | TATAAATACAAAAAT[G/T]TTCCAGGCATGATGG | 114792 |
| rs112752309 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957604 | AAGCACCTCAGGATG[A/T]TATAATTGCAGGTTA | 114792 |
| rs112754842 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101562 | GAAAGTGACTTATAT[A/G]CTGAGTATTGTACAA | 114792 |
| rs112755916 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970955 | GACTACATAATTTAA[A/G]TGATTTAAGATGCTC | 114792 |
| rs112758671 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129159 | TTCTTGAGTGTATCT[G/T]TAAAAGAGCTAGTCT | 114792 |
| rs112759114 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951218 | TAGGACAGGGAAGAA[A/G]CCAGGACCAGCTTGG | 114792 |
| rs112763708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077210 | TCTGATCTGGGTTGT[C/T]CCGCAGAAGGGAAGG | 114792 |
| rs112764563 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065051 | AAAGGAGTCCTAGTC[C/T]GAAGCAATATTGTCT | 114792 |
| rs112774587 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072903 | CCCAAAGTTGTGTGA[C/T]GTCGGACAAGTTACT | 114792 |
| rs112802269 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982939 | AGGAGTGGTGAGAGA[A/G]GGCATCCCTGTCTTG | 114792 |
| rs112813652 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919776 | ATGAAAAATAAAAGA[G/T]CCACATCATCCCCCT | 114792 |
| rs112819233 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992232 | GGATCCATGGCTCCC[A/G]GGACCCAGGGTTGCA | 114792 |
| rs112822235 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060631 | TTGCAGTTTAGAGGG[C/T]CTTCATTGGAGATCA | 114792 |
| rs112826526 | snp | C/G | 0.0252325 | 0.109451 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062397 | AGCTGCACTAATTTC[C/G]TGAATGTCAGTCAAA | 114792 |
| rs112828678 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072525 | TTTTAATTTGGTACA[C/T]AGGGCCTGTCTTTAT | 114792 |
| rs112843221 | in-del | -/AG | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077331 | ATCATTTGTGACAAA[-/AG]AGTCTCAAAGTTCTG | 114792 |
| rs112853679 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987722 | GCAAGGCTACAGTAA[C/T]CAAAACAGCAAGGTA | 114792 |
| rs112863596 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948213 | ACAATGAGCGGTGTG[A/G]ATTTTAGTCAGACTT | 114792 |
| rs112874240 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913444 | ACATGTTTAATACCT[C/G]GCTCTCAGGGGAAAA | 114792 |
| rs112905442 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986708 | GGTGTGCCATTTGCT[A/T]AGACCGTTGGAAAAG | 114792 |
| rs112907048 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946696 | GTAATTTTCATCTTA[C/T]GTTTTTGCCATTTTT | 114792 |
| rs112915891 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915065 | CCTAAAAAGAAAGAA[G/T]AAATGTCACTTGTGC | 114792 |
| rs112922848 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914954 | CCTCCCACCTCAGTC[C/T]CTGAGTAGCTAGGAC | 114792 |
| rs112927880 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916847 | TCCTACACGTTTATA[A/C/G]TGCTATTTTTTTGGT | 114792 |
| rs112963951 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133204 | GAGCAGTAGTGGTTT[A/G]TGACTGGTCTGATAG | 114792 |
| rs113001382 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091985 | TCTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTGTT | 114792 |
| rs113003769 | in-del | -/C | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113182 | TAGGTTAGAATCTTA[-/C]TTTTTTCTTTTCTTG | 114792 |
| rs113005829 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111236 | GAGAGAGATGGCAGT[A/G]TTGCATCCTGTCCCC | 114792 |
| rs113017656 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923902 | AGTGTGAGTTTCTCA[C/G]CATGTTTTACACAGG | 114792 |
| rs113023070 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902884 | GTCAGGTTTGTCAAA[C/G]ATCAAATGATCATAG | 114792 |
| rs113025386 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049530 | TTTAATGTTTTTGGA[C/T]TGCAGTTTACCATGG | 114792 |
| rs113043462 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983780 | CTTCTTTTCTTCTTT[A/G]TTAGTCTTGCTAGCG | 114792 |
| rs113054547 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128119 | TGATTATGACGGTAT[G/T]CCAAAATGATTTGTA | 114792 |
| rs113056466 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984535 | TATAGGTCTCTAAGG[A/G]CTTGCTTTATGAATC | 114792 |
| rs113060129 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071992 | TTTCTATTTCTTGTC[C/T]CTATAATGTACCCTA | 114792 |
| rs113080976 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111816 | TAGTAGAAAGGGGAG[C/G]TGGAAAGGGGATGGG | 114792 |
| rs113087204 | snp | A/C/G | 0.00716521 | 0.0594565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130539 | ACTAGAGGAGATGCC[A/C/G]TGTGTAAATCGCAAA | 114792 |
| rs113088716 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980823 | TAGGTATATTAGTCC[A/G]TTCTCATGCTGCTAA | 114792 |
| rs113089448 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034258 | AAGTTTTTCCTGCAC[C/T]GTATATTGAAAAGCC | 114792 |
| rs113090070 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958976 | TCTCTGCTTGGACCC[C/T]CACAGTACTTATGAA | 114792 |
| rs113096272 | in-del | -/AAAC | 0.249038 | 0.249998 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039822 | AGACTCCATCTCAAA[-/AAAC]AAACAAACAAACAAA | 114792 |
| rs113100409 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967425 | TATATATGTGTGTGT[A/G]TATATATATATATAG | 114792 |
| rs113108879 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125336 | CTAATCCTCTGGATT[C/T]TTGTTGACTTGACTC | 114792 |
| rs113113608 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064062 | TCCTTTATTTTAAAT[A/G]GAAAGGATAAGAGAA | 114792 |
| rs113124015 | snp | A/G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077886 | AAAAGCATACGATGC[A/G/T]AAATCTACTTTTTAC | 114792 |
| rs113124114 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117147 | GTGACTAGATTTGCT[A/G]ATGGGCCCCTTAACA | 114792 |
| rs113132943 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967427 | TATATGTGTGTGTGT[A/G]TATATATATATAGAT | 114792 |
| rs113149350 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062845 | ATAAAACAAAGTTAG[A/G]AGCTAGGGAATGATG | 114792 |
| rs113156826 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982523 | ACTCTCTGCCTTTTA[A/T]TTGGGGCATTTAGTT | 114792 |
| rs113158520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069118 | TGTTCTGTTTACAGC[A/G]TGCACATGTGGATCA | 114792 |
| rs113158674 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106598 | AAATACAAAAAATAG[A/C]TGGGTGGTAATGGCG | 114792 |
| rs113185176 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039444 | ATAATGAGTGCAAAT[A/G]TACAGTTTAATAGAA | 114792 |
| rs113195166 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981091 | AGGAACAGCATGGAG[A/G]TAACTGCCCCCATAA | 114792 |
| rs113199829 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984335 | TAAGTGCAGTGTGGC[A/G]CTGAGAAGAATGTAT | 114792 |
| rs113218206 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104718 | CAAGGAAAATGTTGA[C/T]GCAGTTTTAATTATA | 114792 |
| rs113237676 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979212 | TGTCATGACATATTT[G/T]TCAGGACCTATGTCC | 114792 |
| rs113258128 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084058 | CAGTTATCTGCTGAG[G/T]TGCAAACTATGCACC | 114792 |
| rs113264044 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016763 | GCCAAATCTCATCTC[A/G]AATTGCAATCCCCAT | 114792 |
| rs113274703 | in-del | -/AA | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138566 | CAACAAAAAAACCCC[-/AA]AAAAACAAACAAAAC | 114792 |
| rs113275571 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954400 | ACTCATATTAAAGAG[-/A]AAAAAAACTGGCTGG | 114792 |
| rs113310280 | in-del | -/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981014 | GCAAAGTGGTGGGGC[-/G]GGGGGGCAGGCGGGG | 114792 |
| rs113319261 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104807 | TTCTGGTAAAGGAAA[A/G]TGCTCTGATGCTGCG | 114792 |
| rs113333158 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021154 | TGGAGACCCAGGGGA[A/G]CCAATAGTGTTGGGT | 114792 |
| rs113333600 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986673 | GGACCCTCCAAGCAA[A/C/T]GCACGGGATATAATC | 114792 |
| rs113339439 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914407 | TTATCGGCTCTTCAG[C/T]CTTAACTGTAATTCT | 114792 |
| rs113353587 | snp | C/T | 0.00123768 | 0.0248457 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976201 | GCATTGTTTGTTTCT[C/T]GTAAAATATTGATAA | 114792 |
| rs113362615 | in-del | -/AAA/AAAA | 0.0433465 | 0.140692 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106742 | AGGAGACCCTGTCTC[-/AAA/AAAA]AAAAAAAAAAAAAAT | 114792 |
| rs113398616 | snp | A/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033882 | CAGTTATTTAATTAT[A/T]TATTTATTTTGCTAT | 114792 |
| rs113401324 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953893 | TTATATTGTTATCAA[A/C]AATTCAATCCTCAAA | 114792 |
| rs113424659 | snp | A/T | 0.0437281 | 0.141251 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112766 | AATTTTTTTAATTTT[A/T]AAAAAAAAAAGGAGA | 114792 |
| rs113451263 | in-del | -/AA | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074604 | GTAAGTGAGGGATTT[-/AA]AAAAAAAAAACAAAA | 114792 |
| rs113473683 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959289 | GTGTGGTCTGCAGGC[C/T]CGGGACAGCTTCTGA | 114792 |
| rs113502799 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971327 | ATGAACATCAAACCC[C/T]ATAGGATTTCTGTGA | 114792 |
| rs113504813 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986763 | CGATTTTCCAGGTGC[C/T]ATCTGTCACCCCTTT | 114792 |
| rs113512376 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060527 | CGTCATCATGCTCTA[C/T]ACAGAATCTCACCTC | 114792 |
| rs113520961 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979218 | GACATATTTGTCAGG[A/G]CCTATGTCCAGAATG | 114792 |
| rs113526986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084826 | GTAAAATGTCTCTAG[A/G]ATGTTGCAAAGTAAC | 114792 |
| rs113534018 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016865 | ATGAGTGAGTTCTCA[C/T]AAGAACTGATGGTTT | 114792 |
| rs113552447 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984345 | GTGGCACTGAGAAGA[A/G]TGTATATTCTGTTGA | 114792 |
| rs113569486 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984918 | GATCCTGTCATTATG[A/T]TCTTAGCTGGTTATT | 114792 |
| rs113573748 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061765 | TTTTGGCCAGTCCTT[C/T]GAGGCAGGTGACAGA | 114792 |
| rs113574493 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063097 | ACAGTGACATGATTT[A/C]ATTTGTGGTTTTAAA | 114792 |
| rs113607722 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102728 | GAATGGGTTTCATTT[C/T]TCCTATGGCATCATT | 114792 |
| rs113621224 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980589 | TGTGGATTTTTACAT[C/T]TATGTTCATCAAGGA | 114792 |
| rs113635545 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047971 | AATAAAGTTTATTGT[G/T]TAACACTCTGGCTAT | 114792 |
| rs113636861 | in-del | -/GT | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111032 | ACAGAAAAGTCTTGG[-/GT]GGGGGGGGGGTCTTA | 114792 |
| rs113647437 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113021 | AATAAAAAGGTTAGG[A/G]TTACATTCTGCTATT | 114792 |
| rs113653232 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984501 | TCCCATTATTATTGT[A/G]TGGGAGTCTAAGTCT | 114792 |
| rs113658192 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975402 | TTCTTATGGTGCACA[A/G]TTTCCGAAGTTTAAT | 114792 |
| rs113674756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075421 | TATTTTATCATATTA[C/T]AAGTTATCTGGCCTG | 114792 |
| rs113696398 | in-del | -/ACACACAC | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943037 | GTTCATGCTCCCTCT[-/ACACACAC]ACACACACACACACA | 114792 |
| rs113702720 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986164 | TTTGCCTGGGTATCA[C/G]CAGTGGAGGCTGCAG | 114792 |
| rs113704992 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972000 | TGGGATACAGGCATG[C/T]GCCACCACACCTGGC | 114792 |
| rs113710811 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118340 | ATTGTAGACAAAGGC[C/T]GGGTGCAGTGGCTCA | 114792 |
| rs113714415 | snp | C/G | 0.444444 | 0.157135 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020074 | CAGCCTGCCAAGTAA[C/G]TGGGATTATAGGTGC | 114792 |
| rs113743313 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132080 | CGTGTCAGCATCTAG[A/G]GATTATCCAGGCTGG | 114792 |
| rs113756106 | in-del | -/TT | 0.111928 | 0.208413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107416 | GTATAAGTTAAAAAC[-/TT]AGTTTCTAGTTCTAG | 114792 |
| rs113757778 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986907 | CTGACACTCCCCAGT[A/G]AGATGAACCCAGTAC | 114792 |
| rs113769687 | snp | G/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983490 | CTCTGGTAGAATTCA[G/T]CTGTGAATTCATCTG | 114792 |
| rs113772278 | snp | A/G | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129606 | AAGTCTTCCAGCAGG[A/G]TGCGGTGGTTCACAC | 114792 |
| rs113780211 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060569 | TCCTCCTCTTTCACC[A/G]GATTCTGGCCCCATA | 114792 |
| rs113783638 | snp | A/C | 0.213333 | 0.247296 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029495 | TAATTTTACTGTTTT[A/C]GTTTGTCTTGTGATA | 114792 |
| rs113810159 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986336 | GGACCCACTTGAGGA[A/G]GCAGTCTGTCCGTTC | 114792 |
| rs113815643 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040600 | ACACGTTCCCAGGTG[A/G]TCCTGATGTCGCTGG | 114792 |
| rs113827876 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138563 | AAAACAACAAAAAAA[A/C]CCCAAAAACAAACAA | 114792 |
| rs113828613 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934171 | CAAATACGTGCACTC[C/T]AGAGGTTTGCAACAA | 114792 |
| rs113859435 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961961 | ATAACTATAAGCACC[A/G]TTACTACCGTGACCC | 114792 |
| rs113888971 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069121 | TCTGTTTACAGCGTG[C/T]ACATGTGGATCATCG | 114792 |
| rs113895192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964700 | GTGTTTGCTAGCAAA[C/T]TTTAATTCAATATAT | 114792 |
| rs113898935 | snp | C/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932576 | ATTTCCCCCCCCCCC[C/T]TTTTTTTTTTGAGAC | 114792 |
| rs113909654 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912749 | CTCTGTTTATGTGTC[-/A]CTTTATCCAGGACTC | 114792 |
| rs113921398 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985775 | AGTTAGCCATTCATC[C/T]AATTTTTTTTCAAGG | 114792 |
| rs113927631 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091981 | CAATTCTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs113942027 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974163 | ACCTGCCTCATGGTG[G/T]TGTTGTGCAGATTAC | 114792 |
| rs113950041 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908735 | AGCTGTCCACTGTCC[A/G]CACCCCCCTCCCTTT | 114792 |
| rs113960252 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984569 | GTGCTCCTGTATTGG[G/T]TGCATATATATTTAG | 114792 |
| rs114005843 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102264 | TCAGGATTTCCCTGG[C/T]CATTTCAGCTGACTT | 114792 |
| rs114021876 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961287 | TTAGATAGGAATTTG[A/G]GCAGTAGAAGAAAAA | 114792 |
| rs114025592 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942276 | TGCTGTCCCCCTCAC[A/C]ATCCTTTCCAGCTAC | 114792 |
| rs114066735 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996712 | AAGCAATAACAATAA[C/T]AACTAATTAATATTA | 114792 |
| rs114074903 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967476 | GTGTATATATATATA[G/T]AGAGAGAGATAGGGA | 114792 |
| rs114075186 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094414 | CTCCAAAACTTCTGC[C/T]ACAAGGAAAAATAAC | 114792 |
| rs114112469 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079439 | CTTGCAAATGTAACT[A/G]CACTTGAATATAAAC | 114792 |
| rs114153390 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123064 | GCACTGCATTACGAC[C/T]CATAGACATCTACTC | 114792 |
| rs114232674 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111687 | TTAACAGCTCAGTGG[A/T]GGGTCACCCTCTTGG | 114792 |
| rs114255687 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967748 | AAGCACACCAGTAAC[A/G]ACACAAAAATAATTG | 114792 |
| rs114269799 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917945 | GTTGCAGGGGCTGTT[C/G]CGTACATTGTAGGAT | 114792 |
| rs114300549 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005621 | TGTGGGCATTTATTA[C/T]TATAAACATTCTTCT | 114792 |
| rs114302305 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995462 | TGTGCAGATGACTCC[A/G]TGACTAACTTTCCCT | 114792 |
| rs114350996 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919687 | AAGTAATGCTTTTAA[C/T]TTACTAATGTATTTT | 114792 |
| rs114355391 | snp | A/C/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087634 | GAAAACTGGATGGAG[A/C/G]GGGGCGTGCTATTTG | 114792 |
| rs114411684 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937647 | GAGAGCATGGAATCA[A/T]TGTGTACTCCTGCCT | 114792 |
| rs114441417 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916288 | TGTTATAGGCACATA[A/C]TCCTAAGTTAGGTTT | 114792 |
| rs114452706 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082306 | ACAGGAGTAGATGCA[G/T]GCTATCATAAAATAA | 114792 |
| rs114490679 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115613 | GCTTATACAGAAGGA[A/G]TCTGTGAGGCATATG | 114792 |
| rs114506179 | snp | A/G | 0.0644693 | 0.167566 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040919 | TTCACCTTCGCCTTC[A/G]CCTTCCACCATTATT | 114792 |
| rs114549662 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983518 | CTGGTGCTGGACTTT[A/T]TTTGGTTGGTAAGCT | 114792 |
| rs114602107 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054317 | TCATAAAAACCATCC[A/C]TTTACATTTTATTCT | 114792 |
| rs114629206 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934172 | AAATACGTGCACTCT[A/G]GAGGTTTGCAACAAG | 114792 |
| rs114684102 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138038 | ATTTTTTTAAAACAC[C/T]AAATCCACGGGAGGC | 114792 |
| rs114714023 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122087 | ATCTAATTGATATCT[A/G]CATTATGGTTGATTT | 114792 |
| rs114715651 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094952 | GCGTTAAAGTTTAAA[C/T]GTTTTAGGAGGACCT | 114792 |
| rs114720611 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001210 | TGTAAATGTTGGTTC[A/G]GCAATTTTACCATAC | 114792 |
| rs114723279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959089 | AGAGTGGTGGGGTTT[A/G]GCACCTAGAGAAAGA | 114792 |
| rs114731560 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941675 | AATAAGTGAGCCTGA[G/T]AAAGTATCCTCTCAG | 114792 |
| rs114733065 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117946 | ATTTACTCAAAAGCA[A/C]TATTTAGTGCTTTCT | 114792 |
| rs114736064 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907934 | AATTTTCCATCTTCT[A/C]ACTCAGAAACCAATA | 114792 |
| rs114758674 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942159 | CCAGCGGTTACCCCA[C/G]AGTCACTGTTTGTTA | 114792 |
| rs114770227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134460 | AGCATGTATTTGGTA[A/G]TCCTTCATAGTCTTT | 114792 |
| rs114770493 | snp | A/G | 0.040671 | 0.13668 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112809 | TAAAGCAGGTACATT[A/G]TCATAAATAACAAAA | 114792 |
| rs114781333 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925347 | GATGCCGTTATTTAT[C/T]TTGATATTTAAAATA | 114792 |
| rs114817856 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096485 | CTAAACTTTTTAAGG[A/G]TGTTAATGCCAATAG | 114792 |
| rs114829750 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088673 | ATCATTTCCCAGTGT[A/G]TATGCTTATCAAATC | 114792 |
| rs114837627 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066837 | ATATTGTTCAACTGA[C/T]TTTTAATTTAATGTG | 114792 |
| rs114859279 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108929 | TCCTCTGATAAGGCA[G/T]CAATTTACCATAGTG | 114792 |
| rs114866979 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920284 | GGACCTGTTGGCACT[C/G]AGTCTTCATTCAACT | 114792 |
| rs114888708 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919201 | CTCAATTCTATGAGC[C/T]ACCAGTATCCTTCCA | 114792 |
| rs114919274 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995506 | TTCCTGAGCCCCTCA[A/C]TTCCTGCCTACCAGG | 114792 |
| rs114928890 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930783 | TCTCTGACAAGCCAC[G/T]GTTCCCTCTTTTATG | 114792 |
| rs114932252 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058754 | AGACATAATGCCTGG[C/T]GGTATGGCAGCCAAT | 114792 |
| rs114960816 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916134 | AAAAGTAGAGAGACA[C/T]ACAGGAATCGAAAGT | 114792 |
| rs114977610 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130495 | GTTCCCCTGATGTAA[G/T]TCAAAATGCACTATA | 114792 |
| rs114991261 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015827 | AGGAGGAAAATATGG[G/T]TTCATGGGTCGGCCC | 114792 |
| rs115021477 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086204 | AAATTTAAAGTCTTC[C/T]ATTAGCTGATTAAAC | 114792 |
| rs115075513 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095465 | TGATTAATTCCACAC[C/T]CCTTGGATTCTGGGA | 114792 |
| rs115087195 | snp | A/G | 0.030665 | 0.119967 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907870 | AAAGTTCTGCTTAGC[A/G]CTCAAGATGTACAAC | 114792 |
| rs115087650 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061127 | ACCTGGAGGTCAGGC[A/G]GGGAAAGAATCCTCT | 114792 |
| rs115116051 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047652 | AGACCAGTCCTGAGT[A/G]GAAGAGGTATGAGGA | 114792 |
| rs115122181 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060842 | TATTACTTTGTCACA[C/G]CATTCTGTGTCACCC | 114792 |
| rs115143854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999858 | AGACATTTACCGAGC[A/G]TCTACTACATGCAAA | 114792 |
| rs115154609 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123373 | CGAGTTGTACAGGGA[A/C]GCTTAAGAAAAATGC | 114792 |
| rs115186128 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980611 | CATCAAGGATACTGG[A/C]CTGAATTTTCTTTTT | 114792 |
| rs115190990 | snp | A/G | 0.0134861 | 0.0810011 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142069 | AATAAGATAGAAATT[A/G]TTACTTCTGGTAACA | 114792 |
| rs115245268 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906203 | TAAACAGGGAACCCA[C/G]TTAAGCCTGCTTTGG | 114792 |
| rs115249205 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965454 | AGCATATCAAGTTAG[A/G]CTTATTAGTTAGATG | 114792 |
| rs115250074 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937415 | GTGTGTGTGAACTTA[C/T]TTGCAGATAACTAGC | 114792 |
| rs115338354 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981396 | TGTGAAGTTGGAAGT[A/C]ATATTCCCTTTTTCA | 114792 |
| rs115343885 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990047 | TTTCTCCTGAATTGT[A/G]ATGATCTTCATTCTC | 114792 |
| rs115345937 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006904 | TGACCAACCCCTTCT[C/T]TCTAGATGCTTTTAA | 114792 |
| rs115380009 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977639 | AGGCCCATGAGCAAT[C/T]TGTTGATTGGTTTGA | 114792 |
| rs115441128 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121609 | CAGGAGTCTAATGGC[C/T]TTTAAAATTGGTGTT | 114792 |
| rs115441481 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930193 | CAGACAATAGAGCAG[A/T]GGAGGAGGCATTTTG | 114792 |
| rs115445394 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924059 | CCTTTCTCATTTCTC[A/G]GGCTTGGGGATTTCG | 114792 |
| rs115456652 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985976 | TTTCCAGCTTCTCTG[C/T]TCTGTTTTTTCCCTA | 114792 |
| rs115464776 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906884 | CCCACAACCATGGGC[A/C]CAGTAGCTCTTATAT | 114792 |
| rs115493184 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972590 | TCTGTGGGAGACCTT[G/T]TCCAGTTTTAGGATG | 114792 |
| rs115519200 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059655 | GGCTGCCACCTTGTG[A/G]ATAAAAAGTCCTTAG | 114792 |
| rs115625531 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916881 | CATCATAAAGGAACT[A/G]TTTTTCCATCTAAAA | 114792 |
| rs115634879 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101575 | ATGCTGAGTATTGTA[C/G]AAAAACAACTGGGTT | 114792 |
| rs115646954 | snp | C/G | 0.031825 | 0.122064 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003703 | TAGTTTCAAAGTTCT[C/G]CATATGGCTAGCTAG | 114792 |
| rs115649906 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998506 | TTAGTTTAGCTTTTT[G/T]ATGGTTACTGTAAGC | 114792 |
| rs115653170 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933211 | GGACCCAGTAAGGGA[C/T]GAAATTCCCTTACCC | 114792 |
| rs115682622 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106599 | AATACAAAAAATAGC[C/T]GGGTGGTAATGGCGC | 114792 |
| rs115682877 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128752 | GAATGACCCCACCAG[G/T]CCTCTCTGTTTCTTT | 114792 |
| rs115705635 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112426 | AGGTGCTCCATAAAT[A/G]AATTGTGGTTTTTTC | 114792 |
| rs115729563 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967583 | CTCAAAATGCTCACA[A/G]CATTTCCTTTTAATA | 114792 |
| rs115802444 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065296 | CACCAAGCACTGACT[A/G]TGTGTTCACAGTTGT | 114792 |
| rs115820381 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928457 | GGATGGGTGGGAGGG[A/G]ATGGAGGAAGACAAA | 114792 |
| rs115841368 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962033 | AGTTATGTATTTTTC[A/G]GTCATATAACTTGCC | 114792 |
| rs115866886 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047874 | GGAAAGTAGAACTTC[A/C]AGCACCAAAGGCCTT | 114792 |
| rs115899073 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948206 | ACAATGTACAATGAG[C/T]GGTGTGAATTTTAGT | 114792 |
| rs115900716 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934166 | TCCTGCAAATACGTG[C/T]ACTCTAGAGGTTTGC | 114792 |
| rs115914691 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129540 | ATTACTGAGGGTGAA[C/T]AGGAACCAAATATTG | 114792 |
| rs115930562 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996026 | GCCTCGAGTGGTGGG[C/G]ACAAGTCAGCCTCTT | 114792 |
| rs115932263 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962594 | AAAGTGAAACAAAAG[A/G]AAAAATTCACAGAGA | 114792 |
| rs115935966 | snp | C/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992416 | CTTGATGAAAGTGTC[C/T]ACTTGGATAATCCAG | 114792 |
| rs115973794 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041333 | ACATCAAAATGATTT[A/G]CAGTGGTTTGTGTGA | 114792 |
| rs115987358 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035361 | TTGGGGTAAAAGTAA[C/T]TTACACACCACCATT | 114792 |
| rs116008848 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959030 | AAACAAGCAAATTAT[A/G]TGCCTGGGTGTTGAA | 114792 |
| rs116009895 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978497 | TTTTATGACTGTGTA[A/G]TATTCCACAATATAT | 114792 |
| rs116024501 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120908 | CCCAATCTTTCCTAC[C/T]TCCCATCTGAAAGAG | 114792 |
| rs116051810 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076929 | TGTTTTTGCCATAAA[C/G]TAAGAAATAAAAGCA | 114792 |
| rs116063783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071620 | GCCCAGTCTCACACA[C/T]CTGTTCCTCCTCATC | 114792 |
| rs116064791 | snp | C/T | 0.0655868 | 0.168795 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040959 | CTGAGGCCTCCCCAG[C/T]CATTCTGAACTGTGA | 114792 |
| rs116085616 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131301 | CAGAAGGAATTTATT[A/G]TTTACTTCTCACTGC | 114792 |
| rs116091499 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088883 | CTGTTTTCTTTTCAG[A/G]AACATGCATTTCCTG | 114792 |
| rs116100184 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139691 | TTATTATTTAAAGCC[A/G]GGCTTGTAATTTTTC | 114792 |
| rs116105420 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921179 | TTAATTATGTAATTA[C/T]GATATTCTTTCTTAC | 114792 |
| rs116113867 | snp | A/T | 0.0271762 | 0.113356 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897243 | CCACTTTAATTTTTT[A/T]AAAAAATAAACATAA | 114792 |
| rs116120590 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959426 | AAGTCTGAGATCAAG[A/G]TGTTAACAGGGTTGG | 114792 |
| rs116132268 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000549 | AATGTAGACAAACAT[A/G]ATTTCATTTTTAGAT | 114792 |
| rs116146955 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959637 | AACACAGTCACATAC[C/T]GAGGTATTGGAAGCT | 114792 |
| rs116163137 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107642 | ACACCAAACATGTGA[A/G]GGAAGAAAACAAGGG | 114792 |
| rs116179822 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009020 | TACTTTCTGGCTGTG[C/T]ATATCCTTGGGCAAG | 114792 |
| rs116183422 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965375 | AGTTGGTCTCCAAAC[A/G]ATAAATGTCTGTAAA | 114792 |
| rs116183799 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937311 | AGACATTGGCATATT[A/T]GTCTTATTTGCTTAG | 114792 |
| rs116219009 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004791 | TAATTGATTTGCATA[C/T]GGTGAACCAACCTTG | 114792 |
| rs116219645 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098841 | TTATTGCTTTGTTAT[A/G]TCTTGTTTTTGGTTA | 114792 |
| rs116255644 | snp | G/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006070 | TGAATATCTTTGTTA[G/T]TTTTTTCCCTCAATG | 114792 |
| rs116284554 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977888 | CTAAACTACAAAGAT[G/T]ATACAGAGTATCTGT | 114792 |
| rs116313221 | snp | A/G/T | 0.0103295 | 0.0711199 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139734 | AACATTATGCAGCCC[A/G/T]GCTCAGTAGAGACTC | 114792 |
| rs116317037 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993926 | CATGTCTACCCTTTG[A/C]TCTGGAGAGAGACAT | 114792 |
| rs116350574 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067762 | CCTGATCATCATTCA[G/T]GTGCATTATTTCTCC | 114792 |
| rs116357968 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938806 | CCACCCTGCAGTATA[A/C]TCATGTGACCCACAT | 114792 |
| rs116363890 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126974 | TCAAGAGATATCAAG[A/G]TATCACTGTGTTAGA | 114792 |
| rs116418422 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118635 | AAAAAAAAAAAAAAA[A/G]AATTGTAGACAAAAT | 114792 |
| rs116418952 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080107 | TAAAAGAAATTTGGG[A/G]TGGATTGATTTTTTT | 114792 |
| rs116423011 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074068 | GGCACAGTTGAAGGC[C/T]TCGGGTCACACAGTT | 114792 |
| rs116458154 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135099 | TTTTTAAGTCAACAC[C/G]TGTATTAGTGGAATA | 114792 |
| rs116461268 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090659 | AATTTAAATAGTACT[A/G]GATGTCAAACAATAC | 114792 |
| rs116461775 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086863 | CACTTCCCAAGGGAA[A/G]AAGAAAGATTTGGAA | 114792 |
| rs116461818 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943677 | TTGGCTTTGCGGCCC[C/T]TGTAGTGCCTCGCAC | 114792 |
| rs116490877 | snp | A/T | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036789 | CGGGTGCAGGGTGCC[A/T]GAGTGGCCCCCTCCA | 114792 |
| rs116515146 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076817 | TAACATTTCTAGGCA[C/T]GTACCTTTATTTAAA | 114792 |
| rs116528432 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905269 | ATTATGAAAATAAAG[A/C]ATATAGAACAGGGAA | 114792 |
| rs116550160 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058890 | TTATATTTGTTTAAG[C/G]TGCTTTGTTACATAT | 114792 |
| rs116573416 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080750 | CCATGGAGCTTACTG[A/G]GGGATCAGGGGAGGA | 114792 |
| rs116584483 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931071 | TTCATGCTGAATTAT[A/G]TAAATTTTATGAAAA | 114792 |
| rs116597032 | snp | G/T | 0.021333 | 0.101051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022810 | CTTGTATTAGTTCAT[G/T]TTCATACTGCTATAA | 114792 |
| rs116597165 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980275 | CCAGCTTTTACCTAT[A/T]CAGTATGATGTTGGT | 114792 |
| rs116599273 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945510 | AGTGCAGCACAGTGC[C/T]TACCACTCAATTGTC | 114792 |
| rs116627551 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134120 | CTGTGATAATAAAAA[A/C]AATATACAGCAAAGC | 114792 |
| rs116661583 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111494 | ACCCCTCATGGGACG[G/T]AACATGCAGGTGAGT | 114792 |
| rs116692775 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024093 | TGATTAATCATTTAG[A/G]TAGTATCTGTTAGGA | 114792 |
| rs116694214 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983499 | AATTCAGCTGTGAAT[A/C/T]CATCTGGTGCTGGAC | 114792 |
| rs116695436 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942832 | CATCTCTAGTTTTTT[A/G]TTGTCCTCATTCTGC | 114792 |
| rs116727348 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927908 | GAGCAAGCTACTTCC[A/T]TATCGGCTTCACAAT | 114792 |
| rs116732401 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113622 | CTGAGACGGAAAAAA[A/T]GTTCCTCACATGGGC | 114792 |
| rs116743762 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969307 | TCTTACCACAGCCTC[C/T]TCTCCTTTTTCAAAA | 114792 |
| rs116747140 | snp | C/T | 0.030278 | 0.119257 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040307 | AAATTAGCATGGGGT[C/T]GTATTTTTTTTTTCC | 114792 |
| rs116747516 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108428 | TTTTATGATGCCCCA[A/G]TGATAAATCAGCTTT | 114792 |
| rs116772439 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130695 | ACTTATGAGGCACTC[A/G]TTGCTGTTTTCTGAC | 114792 |
| rs116788879 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105605 | CAGCAGAGCTATCTG[C/G]AACCAGATTTTACAT | 114792 |
| rs116813405 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924102 | GGGTTGGTTCCCCTG[A/T]CGTTTCTTAAAGTTA | 114792 |
| rs116830072 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939122 | TGGCTTGCATGGCCC[A/G]CCTCTCCCCTCTTCC | 114792 |
| rs116839582 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941938 | AAATGGTCCAGATCC[A/T]TATTCCTATGCAAAA | 114792 |
| rs116856639 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102028 | TTCACATGTCTGATC[A/G/T]CATTCAGTCTTCCGT | 114792 |
| rs116868077 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921626 | GTGACAGAAAACCAC[A/G]ACACTGGCATTAAGA | 114792 |
| rs116902294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128521 | CTGGCATATTGTTTA[C/T]GGTGGGTACTGGCAA | 114792 |
| rs116983239 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977773 | AGAAGACAGCCTTTT[C/T]TAAAAAGCGTATTAA | 114792 |
| rs116994257 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011399 | AATGAGACAAGTTTT[C/T]TAATAGTGATGACAA | 114792 |
| rs117022471 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933406 | GTCAGCAGCTATTGG[A/T]GTAAGACTCCTTTGT | 114792 |
| rs117032640 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104706 | AGATCTGTCTTACAA[A/G]GAAAATGTTGACGCA | 114792 |
| rs117035720 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071361 | GCTCCTCTCTTTCTC[A/G]GGGCTCTCTCCTATT | 114792 |
| rs117037925 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057993 | CCCCATTCTTGAAAA[G/T]ACTATCTTTTATCCA | 114792 |
| rs117044252 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102671 | TTATAGGGTGTTATT[C/T]TATAACTGTACATGT | 114792 |
| rs117060625 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908885 | GAAGACCAAAGCTTC[C/G]TACTTGTGCCTATTT | 114792 |
| rs117119785 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059020 | AGGCACCTGGAGTTG[A/T]GCTGTTCTCCCAAGT | 114792 |
| rs117123951 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976981 | TCATGGTCAGTACAT[A/G]CATGCGGCTAATGAA | 114792 |
| rs117128077 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903907 | AAGAATTATAAATGT[C/T]ATGTTATTTGTTCTT | 114792 |
| rs117130336 | snp | A/C | 0.0498117 | 0.149749 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082339 | TCAGTTTAGGCTGGG[A/C]GCGGTGGCTCACACC | 114792 |
| rs117157308 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066035 | CAATATTGTTACGTG[A/G]TATAGGAAAGCTATT | 114792 |
| rs117189678 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090210 | TTGAATGGATAATAA[A/G]ACATCCTACTATTCC | 114792 |
| rs117195980 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934195 | GCAACAAGGCTGGTC[C/T]TCAGAATGACCTGAG | 114792 |
| rs117203043 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052088 | TTACTCTAAGCACCA[A/G]TAGAATTTCCTAACC | 114792 |
| rs117269521 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925095 | GGAGGCTGCTGGTGC[G/T]CCAAGTGGGGGCAGA | 114792 |
| rs117275168 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084680 | GTTTTGGAAAAAGAG[C/T]GGAGTCAGTCTGTCT | 114792 |
| rs117295348 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932025 | TTTGATAGAGTCTCT[C/T]GTTCACTTGTTTCCT | 114792 |
| rs117330859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905985 | CAATCCATGACCTTG[C/T]AGGCACAGCTCTGCC | 114792 |
| rs117339200 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966301 | ATAATTTATTTTTCT[A/G]GTCAGAGTTACTCCA | 114792 |
| rs117340950 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946348 | AGCACTTATTATCTC[A/G]TGGCACACCATATCA | 114792 |
| rs117345426 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003302 | GTATGTCTTCTTTTA[C/G]AAAGTGTCTGTTCAT | 114792 |
| rs117370276 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093692 | CTGAGGGTCTTTCTT[G/T]ATCAGAGCCCAGAAA | 114792 |
| rs117387465 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019697 | GAGACATCCAAAATA[A/G]GAGCTATGCTTTCAA | 114792 |
| rs117398729 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082341 | AGTTTAGGCTGGGAG[C/T]GGTGGCTCACACCTG | 114792 |
| rs117475588 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107643 | CACCAAACATGTGAG[A/G]GAAGAAAACAAGGGC | 114792 |
| rs117505944 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029136 | GATTTGTGTCCTTTT[G/T]TTATTCCACCCTTTC | 114792 |
| rs117532663 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084094 | AAGGAGTTCTTGATA[A/C]TCTCAGGTAACCAGA | 114792 |
| rs117550124 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070021 | GACAATAACTTCTCC[A/T]CAAGATTGAGGAGAA | 114792 |
| rs117563673 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051301 | TCTCCTTCCAACTCT[C/G]AGCACCTCCCACCCT | 114792 |
| rs117601463 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907701 | GGATGCCACAACTTA[A/G]CTCGCCCAGCTCATT | 114792 |
| rs117603278 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995776 | AAGCCCTATCCTGAT[C/T]ACCCTCTGCCACCGC | 114792 |
| rs117624209 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911977 | TTGCTGGCTTCAATT[C/T]CCATCTTATTTTGAT | 114792 |
| rs117639131 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906883 | ACCCACAACCATGGG[C/T]ACAGTAGCTCTTATA | 114792 |
| rs117656595 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896220 | CCCAGGACTTACATA[A/G]TACAGAATATGGATT | 114792 |
| rs117660763 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005555 | GTTCTTTTCCTATTT[C/T]TTCTAGGTGTGATAT | 114792 |
| rs117667240 | snp | C/G | 0.0653867 | 0.168576 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018151 | TAATTAATATTGAAT[C/G]GAAACTTTTTTCAAT | 114792 |
| rs117673290 | snp | A/T | 0.0883596 | 0.190715 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082622 | CCATCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 114792 |
| rs117702894 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035443 | ATTTATGTTTTCTTA[C/T]GCTTTCACGTTACTG | 114792 |
| rs117713617 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974132 | TTTCTATCTGTAAAA[C/T]AGAGATAATAATAGT | 114792 |
| rs117718062 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018361 | GGACACCAAGGCAGG[C/T]GGATCGCCTGAGGTC | 114792 |
| rs117719946 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052421 | CTTTGTTTTTATGGG[C/T]GTAGCATTCCTGGAA | 114792 |
| rs117720017 | snp | G/T | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057151 | ATATGTACAAAAAAT[G/T]CAGTTTTCCTATGTG | 114792 |
| rs117737534 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058674 | TTTTTCTGATAAACA[A/G]TGCCAGACTCAGCTG | 114792 |
| rs117743308 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132515 | AGTACTGGGAGGCAG[C/T]GATTAGTTGCTGCAA | 114792 |
| rs117751303 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993588 | GGCATAGACACAAGT[A/G]GGGGAACATTTTGTT | 114792 |
| rs117761633 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081359 | TGCCTCCTGGAGTGT[A/G]GAAGCCACATAGAGG | 114792 |
| rs117782187 | snp | C/T | 0.030278 | 0.119257 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985741 | GTCCTTTAAGGACTT[C/T]TCTAGAATTGGTTAT | 114792 |
| rs117804808 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903220 | TTTTTGGAAAGAATA[C/T]GATCATAAATATGGA | 114792 |
| rs117868733 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032397 | ATATAGATATACATT[A/G]TTTAAGGAATTGTGT | 114792 |
| rs117882886 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084448 | AGCATTTCTGCAGAA[A/G]CTCTTCAAAAAGGTG | 114792 |
| rs117883448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091738 | CTTATTGTTAACTCT[C/T]GATAGTTGTATGCAC | 114792 |
| rs117891555 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970596 | TACCACATATGGTTT[G/T]CTCACCATTTTATCC | 114792 |
| rs117894429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029396 | TTTTTAGCATATAAG[A/G]TGGATCTTTATGTGG | 114792 |
| rs117908219 | snp | C/G/T | 0.00904371 | 0.0666347 | KLHL32, NDUFAF4 | 6 | allele_origin=T(germline)/C(germline) | 6:96897682 | ACTAATCTGCTCTCG[C/G/T]AGGAGGCTGTTGGTA | 114792 |
| rs117997949 | snp | A/T | 0.0452528 | 0.143452 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897244 | CACTTTAATTTTTTT[A/T]AAAAATAAACATAAT | 114792 |
| rs118010222 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115664 | ACATGTGTTTTCAAT[A/C/T]TTAGTTTTGAGAAAG | 114792 |
| rs118019237 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973871 | GGGATTAAGGTGCGC[A/G]CCACCATGCCTGGCT | 114792 |
| rs118022407 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106168 | TAAAGGAATTAGAAT[C/T]ACAATATGAGGACTT | 114792 |
| rs118060297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981090 | CAGGAACAGCATGGA[A/G]GTAACTGCCCCCATA | 114792 |
| rs118096987 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090035 | TGGCAAAGAGGGACC[A/C]TGTCACCTGATTTGG | 114792 |
| rs118098628 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013792 | GGAAGAAAACAGCGT[A/G]TTATGGGAGTCAAGC | 114792 |
| rs118111795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979876 | GTAGAGCTCTTTTAC[C/T]TCTCCGGTTGGCTGT | 114792 |
| rs118141573 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938440 | CTGGGCTCCACCTTC[C/T]GGCATGCTTCTCGTG | 114792 |
| rs118144526 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104683 | GTTAATGTGCAATCT[C/T]CCTTGAAAGATCTGT | 114792 |
| rs118185523 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975566 | AGGTGGGGAAGGAAT[C/T]AGGGAATTAGAGAGA | 114792 |
| rs118188443 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066034 | TCAATATTGTTACGT[A/G]GTATAGGAAAGCTAT | 114792 |
| rs137887833 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900161 | GTGAGTCCTTATGCA[A/C]GTAACTTAATGTGGT | 114792 |
| rs137891424 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091301 | TGAACAAATCATGGC[C/T]TCTGTGCCTGCCTCC | 114792 |
| rs137908084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061228 | TGTTTGCAAATCTGG[A/G]GAAGCCCCAGCTCTA | 114792 |
| rs137924006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094863 | TCTTTGTGTGTGTTC[C/T]TGTTGATGAGGAATG | 114792 |
| rs137930248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972094 | TGACCTCAGATGATC[C/T]GCCCACTTTGGCCTC | 114792 |
| rs137935430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048915 | GTAGTGTTAAGACTA[C/T]TCAGTGGTTTAAATA | 114792 |
| rs137949939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977613 | AGCCTAAATGTTACA[A/G]ACACCAACTTAGGCC | 114792 |
| rs137950297 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051029 | ACAAACAAACAAAAA[-/AC]ACATGTGTTTGAACA | 114792 |
| rs137954265 | in-del | -/CACA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068021 | ACAGACACACACACA[-/CACA]CACACACACATACAC | 114792 |
| rs137957757 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051963 | GAAGATATGCAGTCT[A/C]TTCATCTGGCTTGGT | 114792 |
| rs137958585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939480 | GAGAGGTTCATGGCA[C/T]TGTTAAAAGTATAAA | 114792 |
| rs137978430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130521 | CTATAAAATGCAACA[C/T]AAACTAGAGGAGATG | 114792 |
| rs138000701 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995790 | TCACCCTCTGCCACC[A/G]CGTTAAGTTCATATG | 114792 |
| rs138037732 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064902 | AGGGCGGCTGCAGCT[C/T]TTGCATCCAATCACA | 114792 |
| rs138040296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907123 | GAATCTTGTTATTTA[A/G]CAATGCAGCTTTGTT | 114792 |
| rs138045226 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985306 | GGCTGCCCTTATCAT[G/T]TTTTCCTTCATTTCA | 114792 |
| rs138081542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911051 | TAAAACTGTACACCT[A/G]ATGCTTTGATATTCT | 114792 |
| rs138081952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138406 | TAGCTAGGCGTGGTG[A/G]TGTGCACCTGTGGTC | 114792 |
| rs138123575 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074706 | CAGCAATCTGACTTT[A/G]TGTACTAGAGCAAGT | 114792 |
| rs138146377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095889 | AAACAAAAACTCTGA[A/G]ATTTTGCAGAAAGTC | 114792 |
| rs138149979 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028681 | TCTCAGTTGGGGTGT[C/T]CTTAGAAGTTTGTGA | 114792 |
| rs138161588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956066 | GAAGGTGAAAGGCAC[A/G]TCTCATATGGTGGCA | 114792 |
| rs138198636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018676 | ATATTAGTCAGATGC[C/T]AACAAAAACATATGT | 114792 |
| rs138202952 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099552 | AGCTACTACCTTCTA[C/T]TCATTCCTTCCTCCT | 114792 |
| rs138221706 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982329 | TGTCTTCTTTTATTG[A/G]TGTTGCCTTAAAGTC | 114792 |
| rs138222606 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023332 | GCATTGACAATCTAT[A/G]AACTATAAGCTGACA | 114792 |
| rs138244102 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896273 | ATGTATTCTTTGATC[C/T]TTCTAATTTTAAATA | 114792 |
| rs138247974 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080235 | CTTTGCCTTTGTGTG[C/T]ACGTGTCAGAAGGCC | 114792 |
| rs138254704 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111504 | GGACGGAACATGCAG[A/G]TGAGTGAGTGCAGGA | 114792 |
| rs138261410 | in-del | -/T | 0.27008 | 0.249192 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043734 | TTGTTATCGATTGTC[-/T]TTTTTTTATAGTAGG | 114792 |
| rs138305614 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004556 | TCTTGTCTTGTTCCC[A/G]TTCTCAAGGGGAATG | 114792 |
| rs138316148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994659 | TGATTAATGAATGAT[C/T]AGTTGCGTGCAAAGT | 114792 |
| rs138317522 | in-del | -/ATC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057170 | TTTTCCTATGTGAGT[-/ATC]TTTTTTTTTTTTTTT | 114792 |
| rs138346411 | in-del | -/AG | 0.498749 | 0.057221 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916367 | CAAATATAGAAGTAC[-/AG]AGTCTTTCTCAGGAC | 114792 |
| rs138351776 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986974 | TCGCTCACGCTGGGA[C/G]CTGTAGACTGGAGCT | 114792 |
| rs138353445 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970472 | CTTTTAAAAGATTAA[C/T]TTGTTCTCATCCTTC | 114792 |
| rs138392473 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098419 | TTTTTACCTAGCCTG[C/G]GACATTTTTTCTCAC | 114792 |
| rs138422546 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981920 | GTCTGAGAGTGTGAT[C/T]GGTATAATGTCAGTT | 114792 |
| rs138425001 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931738 | CTCCAGAAAAGAATA[A/T]GGTAAAAAATGTTTT | 114792 |
| rs138447389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056844 | CGGAGCTCGACACCA[C/G]GCTGGGCAACATAGC | 114792 |
| rs138453173 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934471 | CAACAAAAAAATAGC[A/C]AGTTAAATCAGTTCT | 114792 |
| rs138522477 | in-del | -/A | 0.222928 | 0.24853 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927476 | ATCTTGTAGTGAGGT[-/A]AATACGTCTTGAGAA | 114792 |
| rs138537308 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041281 | TGTATATGGTGAGGA[A/G]TGCCATCCTGTGTGT | 114792 |
| rs138543658 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135873 | ATAGCTACATGTTCA[A/G]AAGTAGGCCACTTCT | 114792 |
| rs138548618 | snp | A/C/G/T | 8.25414e-05 | 0.00642382 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064669 | GGATGTGCTAGCAGC[A/C/G/T]GGCAGTCACCTACAG | 114792 |
| rs138556958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935169 | AGAATTCATTTTGTG[A/G]TGTGTGACTAGCTGA | 114792 |
| rs138579067 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916640 | TGAAGGCCTCTGTGC[A/G]CATAAAAATTAGAAT | 114792 |
| rs138579543 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046988 | TGAAATGTACGTATT[C/T]TAAGTGTCTGAAAAT | 114792 |
| rs138584945 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000970 | CAACTATATGACATT[C/G]TGGAAAAGGCAAAAC | 114792 |
| rs138587901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024653 | CATTTAATTTTCATT[A/G]TCGCGTTTATAATTA | 114792 |
| rs138590395 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140457 | TACTATCTCTTTTAA[C/T]AATGCATAGGAATTC | 114792 |
| rs138597365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105861 | TCATCTGATGAGAGC[C/T]TGCTTTTTAAGGGCA | 114792 |
| rs138607789 | snp | A/T | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142432 | TTGCTAGCTTCCCAA[A/T]CCAACTGTTTCTAAC | 114792 |
| rs138615324 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004983 | TTTGGTATCAGGATG[A/C/G]TGCTGCTCTCATAGA | 114792 |
| rs138618158 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901682 | TCATCCCATCACCCA[G/T]GTATTAAGCCCAGTA | 114792 |
| rs138641418 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069818 | GTTAAAAATACTTTC[G/T]TCGGGGATTAAATTT | 114792 |
| rs138677469 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118388 | CTTTGGGAGGCCGAG[G/T]CGGGCGGATCGCCTG | 114792 |
| rs138680943 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017790 | GACTAGAAGGACACA[A/G]TGGTTATGAAACAGA | 114792 |
| rs138690480 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950515 | TAAAAAAAAAAAACC[C/G]AGACACTTTGCTTTA | 114792 |
| rs138727852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955153 | CCAAAGGCTCCACCT[C/G]CCAGTACCATCACAT | 114792 |
| rs138734446 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987241 | CTTACTTATTTCTTG[C/T]CTTCTGCTAGCTTTT | 114792 |
| rs138774633 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105765 | AAGACAAAAAAAAAA[-/A]TACTTGTTACTTTTA | 114792 |
| rs138817390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070609 | ATTGACTGTATCTTC[A/G]TTTGTGAGGATTTTA | 114792 |
| rs138845344 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951493 | GCATGTTGGACAGTG[C/T]GCCACCCCACACCCT | 114792 |
| rs138864843 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024903 | AATATCACTTTATTT[G/T]TCTGCCATATCTTTT | 114792 |
| rs138874000 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041777 | GTAAGTAAAGCAATT[G/T]GATTTTTTAATATGA | 114792 |
| rs138890361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955430 | CTCTTGTTCTCTTTG[A/G]TCTTGGGGGTTTATT | 114792 |
| rs138925355 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061391 | CACTTGGCTTTATGT[A/G]TCTAGCATTTTCTTG | 114792 |
| rs138957282 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939754 | CTTTATCAGAAATGC[C/T]GAGAAGCCATTGAGG | 114792 |
| rs138961852 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000095 | AAGTCAAAGATAAAA[A/G]CATAAGCAAAGTGTA | 114792 |
| rs138965259 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064506 | CATAAAAAGGAACAG[C/T]GTTAATTGAAATAGA | 114792 |
| rs138966865 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011554 | TTAAATTATAAAATT[A/G]TTGAATTTCTTGTCA | 114792 |
| rs138970092 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036508 | TACAGACTGGCTTTG[A/G]TGGGGAAGACTTTCA | 114792 |
| rs138994239 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976769 | ACACCTGGCTAATTT[C/T]TGTAGTTTTAGTAGA | 114792 |
| rs139004028 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119654 | AGGATAAAGCCTTTC[A/T]TAGTCTAATACTAAT | 114792 |
| rs139031023 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964187 | AGGAGGGGAACTGCA[C/G]GAGACTGGCCTGGAT | 114792 |
| rs139044246 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086067 | CTATCTTCCTCCTCC[A/G]TATTACAGCCTGTCT | 114792 |
| rs139045725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988996 | CATTAGGAGATATAC[C/T]TAATGTTAAATGAGA | 114792 |
| rs139055390 | snp | A/C/T | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966836 | TATCCAGAACAATTA[A/C/T]TTGTTTGTTAAAGGA | 114792 |
| rs139095769 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919208 | CTATGAGCCACCAGT[A/G]TCCTTCCAATTAAGT | 114792 |
| rs139096908 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968364 | CCCCTACAGCAAAAA[A/G]CAAAAAACAAAAAAC | 114792 |
| rs139104885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042942 | TCCCTCAGGGTGTGA[G/T]TGAGTTCTCACTGTT | 114792 |
| rs139129149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127346 | GTATCTCATTCTTAT[A/G]TTGGAATATCCTATT | 114792 |
| rs139187336 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054930 | GGCAACAGAGTGAGA[C/T]CCTGTCTAAAAAAAA | 114792 |
| rs139188756 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921881 | GATGATAGATGAAAA[A/G]AATGCTGCAGAAACT | 114792 |
| rs139194086 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124954 | ACACATCTTGACTAT[A/G]TAGGCATTTCAGCCT | 114792 |
| rs139215575 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933039 | ATGTGGGTGGAATTC[G/T]TTGACCAGCACATCA | 114792 |
| rs139229205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927694 | TCCCCCTCTGGAAAG[A/T]TGCCTTAACAGTAAA | 114792 |
| rs139255637 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075652 | GCCAGACCTTACCGC[A/G]CATCCACACCAGCCC | 114792 |
| rs139283964 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907909 | CTTCTTTGTATGTGA[A/G]TGACTAGTTAATTTT | 114792 |
| rs139293105 | in-del | -/TTTG | 0.460925 | 0.134204 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003364 | TTTTTTGCTTGTTAA[-/TTTG]TTTAAGTTCCCTATA | 114792 |
| rs139322896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079237 | TGAGATATTGAGAGA[C/T]ACCGCAAAGGCCATG | 114792 |
| rs139341110 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994935 | GGGACCTAATCTGTC[C/T]GTTCTGTTCACCATT | 114792 |
| rs139375657 | in-del | -/A | 0.110872 | 0.20771 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915932 | TCCTTTCCCAAAAAA[-/A]GAAAGAGATCAACCA | 114792 |
| rs139379393 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067383 | TAGCCTTCTCACAGG[C/T]TCTCAAAGCATGTGT | 114792 |
| rs139381044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961552 | CTGTGGTGACAGTTT[C/T]TGCAAAAAAGAAAAG | 114792 |
| rs139382385 | in-del | -/T | 0.046775 | 0.145601 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993309 | TGGAGGCTAGTGATC[-/T]TAAGTTGGCCTTGTT | 114792 |
| rs139389134 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083166 | GGAGGCCAAGGTGGG[C/T]GGATCATGAGGTCAG | 114792 |
| rs139400631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081640 | ACTTTCCACTCCAAG[C/T]CAACTCCAAGTTAGT | 114792 |
| rs139483144 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031723 | TGATTTTTATAATGG[G/T]GTCATTCCATAAAGT | 114792 |
| rs139612752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940849 | AATACATTCATAGAA[C/T]AGCCGAGAGAAAAGA | 114792 |
| rs139618814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091780 | CTTCGCAAACCTTTG[C/T]CAATCCATGTGATAC | 114792 |
| rs139629318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97008009 | GTATGTGAATTGCCT[A/G]GGATGTGGGACCAGT | 114792 |
| rs139640874 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944932 | CTTTTCTTTATTGGA[A/C]GAATGATCGTCTTTA | 114792 |
| rs139646157 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983413 | ACGAGTTAGGGAGGA[G/T]TCCCTCTTTTTCTAT | 114792 |
| rs139650241 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973194 | TGATCCTGTGAAATT[G/T]TGCAGCATCACTATT | 114792 |
| rs139658920 | in-del | -/ACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943037 | GTTCATGCTCCCTCT[-/ACAC]ACACACACACACACA | 114792 |
| rs139669894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013265 | TGGTATCAGAAAAGT[A/G]CACTGAGCTAGTGTT | 114792 |
| rs139669986 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973870 | TGGGATTAAGGTGCG[C/T]GCCACCATGCCTGGC | 114792 |
| rs139675421 | snp | A/G/T | 0.0121515 | 0.076995 | KLHL32, NDUFAF4 | 6 | allele_origin=G(germline)/A(germline) | 6:96897691 | CTCTCGCAGGAGGCT[A/G/T]TTGGTAGAGGGGTGT | 114792 |
| rs139710100 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102386 | AATGTGATACAGAAG[A/G]GTTTTCTTTTATTGA | 114792 |
| rs139752388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103153 | ATGGAGGGAATGGTA[C/G]ATTTAAAGACAGTCC | 114792 |
| rs139754997 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059185 | TTGTATAAGGAGTGG[A/G]TTTAGAGTTGGATCT | 114792 |
| rs139758262 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978572 | AAGTTGATTCCATGT[A/C]TTTGCTATTGTGAAT | 114792 |
| rs139759146 | in-del | -/CACACA | | | cds-indel, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924802 | ACACACGCACGCAGG[-/CACACA]CACACACACACACAC | 114792 |
| rs139770176 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982788 | ATTTTGGGCTGAGAC[A/G]ATGGGGTTTTCTAGA | 114792 |
| rs139794231 | snp | A/G | | | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114347 | CTGGGTGCCATGGAG[A/G]AATACCTCTATGCAG | 114792 |
| rs139796112 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992612 | TATCAATACGTGCGC[A/G]CATGTGAGTGCAAGA | 114792 |
| rs139796146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049296 | GGGCCATTATTAAGT[A/G]AAATAAACACAAGCA | 114792 |
| rs139798222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131543 | AGGATGAAAGTAACA[C/T]GGTGAACAACTTACC | 114792 |
| rs139811622 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936782 | CAGACCCTGTATACC[A/G]TCTATCCCTCTCTTA | 114792 |
| rs139815512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996399 | ACAACAACAACAACA[A/G]TCTGTGTTTCATGTA | 114792 |
| rs139822759 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928207 | ATCAGGTCAGTCCCT[A/G]GGTAGTAGGGGGATT | 114792 |
| rs139831319 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139147 | AAGCAGAGAAGGCAA[A/G]GAAGAAGTATTCTAT | 114792 |
| rs139892134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026476 | GGGAAATGGTTGCTT[A/G]GCAACTAATGGGGTT | 114792 |
| rs139903200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093292 | TTACAAGCCTAGAGG[A/G]CTTTATATTTTAAAG | 114792 |
| rs139904415 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920185 | GGTCAGGGAAAGGGA[C/G]CTGGTCAAGGAAAAT | 114792 |
| rs139961416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043705 | AAGGTTTTTCTCCAC[A/G]CCCTCATCAATACTT | 114792 |
| rs139968766 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096437 | AGTAGAAGCTTATTT[G/T]CACCACTCCAAGCGT | 114792 |
| rs139973874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903148 | TTGGTTCCTTGAGAA[C/T]ATAAAATCTGACAAA | 114792 |
| rs139988229 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922473 | CCTAAATTAGGCAGA[C/G]AGTTTTCAGTTGCAA | 114792 |
| rs140008935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066262 | CAGTTTGGTTAGAGC[A/G]TTAGTTATCATGATG | 114792 |
| rs140016786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980088 | TGGAGAGTTCTAAGT[A/G]TGGAATCACATCATC | 114792 |
| rs140036072 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946251 | AGAATAGATATATAA[A/T]ATCTATTTTCAGTTT | 114792 |
| rs140052984 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030624 | TGCTTTCATATTTCT[A/C]AGCAGAACTTTATCC | 114792 |
| rs140054692 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112278 | TTGTCTGGGAGATCT[A/T]CTTTAATGTAAGTGC | 114792 |
| rs140054930 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896923 | ACGCTTAACACAAAC[A/G]CTTTCTTTTATTTTC | 114792 |
| rs140072994 | in-del | -/AG | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139352 | GGCATGAAAAGACTC[-/AG]TGCTCCATGCTTCCT | 114792 |
| rs140078367 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982965 | TGTGCCAGTTTTCAA[-/A]GGGAATGCTTCCAGT | 114792 |
| rs140089382 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037009 | AAAAATGTTCAATTT[G/T]TAAAATTTATGATAA | 114792 |
| rs140090799 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985991 | CTCTGTTTTTTCCCT[A/G]TCTTTGTGGATTTAT | 114792 |
| rs140101728 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901866 | CTGTGTTAGTTTGCT[A/G]AAGATAATGGCCTCC | 114792 |
| rs140110010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908994 | GGGTCCGTTTGAAGG[A/G]TACAGAGACCTGATA | 114792 |
| rs140143733 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104673 | AGCTATAATGGTTAA[C/T]GTGCAATCTCCCTTG | 114792 |
| rs140149040 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913493 | GCTCATTTTCATGGT[A/G]TAAACAGTCCTACCT | 114792 |
| rs140185595 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987605 | TGGAAAAAACTACTT[G/T]AAAGTTCATATGGAA | 114792 |
| rs140188983 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059902 | GTAATACTATACAGG[-/A]AAAAAAAAATACCAA | 114792 |
| rs140195232 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953614 | CAGCCTGGGTGACAG[A/G]GTGAGACTCCATCTC | 114792 |
| rs140200517 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941780 | TGTCCTTTACTGATC[C/T]CTTCCATCTAAGCAA | 114792 |
| rs140211446 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060701 | GTGACCAGAGGACAT[C/G]TTGGCACACAGTATT | 114792 |
| rs140236203 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915469 | ACAAGCCAGGTGCCC[A/G]AGAGCTCAGTGGAAG | 114792 |
| rs140246562 | snp | A/C/G | 6.58994e-05 | 0.00573986 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114053 | GGTGGGAAAAAGCGC[A/C/G]AGGTCTGCAAGGTCA | 114792 |
| rs140254052 | snp | A/C | 8.23676e-05 | 0.00641693 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113865 | GCTTTGGCCTAATGG[A/C]TGTGGATACTCTCCA | 114792 |
| rs140256297 | snp | A/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140684 | CCCTCTCTTAAAGGA[A/T]ATTGTTATTTTATTC | 114792 |
| rs140269890 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046340 | CCAATTAGTCAAACC[A/G]AGTCCTACTAATTTC | 114792 |
| rs140303137 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923179 | AAATAAATAGCTGCT[A/T]TTTATTCTAAACAGA | 114792 |
| rs140307645 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993358 | TAGGCTGTTGGTTGG[G/T]GTGGTAAGGGAAGCT | 114792 |
| rs140318874 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073776 | CTGGGAGAATGCTAT[C/G]CATGTGTCTCATTTC | 114792 |
| rs140326190 | snp | C/T | 0.00304503 | 0.0389005 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114472 | ATCCCTTTCATGCCA[C/T]GCTGGATATGTGGCT | 114792 |
| rs140345969 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027809 | ACAAAACTTCGAGCA[C/T]TGGCTTCAAGCACTA | 114792 |
| rs140347089 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955234 | ACAGCATGAACCTCA[C/T]ACTCATACCATTGGT | 114792 |
| rs140349282 | in-del | -/TATT | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025982 | CCTAGAAGAAAAAAC[-/TATT]TATCTTTCTTTTAAT | 114792 |
| rs140383875 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985302 | CTCTGGCTGCCCTTA[A/T]CATTTTTTCCTTCAT | 114792 |
| rs140385712 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067774 | TCAGGTGCATTATTT[C/T]TCCCACAAAAGTCTT | 114792 |
| rs140386617 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033647 | ACATTACAACCAACA[A/G]TAAACAAGGATTCCC | 114792 |
| rs140391539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119298 | TGGCTGGAACTTCTT[C/T]ACTTTCCTCAAAACC | 114792 |
| rs140402853 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958556 | TAAAACACAAGGCTG[A/G]TAGTGTTGGAAGGGG | 114792 |
| rs140426546 | in-del | -/AAAC | 0.258565 | 0.249853 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931110 | GCTCACCAGGATAAA[-/AAAC]AAACAAACAAACAAA | 114792 |
| rs140427414 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934412 | ACCAGCCAGGCCATC[C/T]GGATCTGGGCCTCAG | 114792 |
| rs140432821 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004240 | CTTTTTATGGCCATC[A/G]TGAATGTGACTGAGT | 114792 |
| rs140438609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123348 | ATCCATTTGTCACAA[C/T]ATTTTGTGGCGAGTT | 114792 |
| rs140515288 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057997 | ATTCTTGAAAAGACT[A/G]TCTTTTATCCATTAT | 114792 |
| rs140529666 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933280 | GGGCACTGTATTCTT[A/G]GAATTCTGCTTCCTC | 114792 |
| rs140545289 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985028 | TTGTTCCTTTCCATT[-/G]TTAGTGCTTCCTTCA | 114792 |
| rs140600325 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936222 | AAGAATGCTAAGAAT[C/T]AGGATTTTAAATAGA | 114792 |
| rs140607938 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139792 | TAAATGCCATATTTT[A/G]TTCAAGGTGATACGA | 114792 |
| rs140637737 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009625 | TGTTGTTGTTACATA[C/T]GCTAGTTTACTGTTT | 114792 |
| rs140645590 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094616 | TGGCATGTTGATGAA[A/C]TGCAAACCTATTTTG | 114792 |
| rs140684446 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976798 | GAGACGGGGTCTCAC[C/T]AAGTTGGCCAGGTTG | 114792 |
| rs140685651 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016494 | TTCTCACTTTTGGAA[C/T]GAGTGTATTTACCCA | 114792 |
| rs140704171 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981007 | AGCAAAGTGGTGGGG[C/T]GGGGGGGCAGGCGGG | 114792 |
| rs140712131 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958340 | AGTAATTAACTGTGA[A/C]CTGGGAGGATCAGGG | 114792 |
| rs140736221 | in-del | -/TTTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135319 | TTTTTTTTTTTTTTT[-/TTTC]TTTCCTGAGAGTGTC | 114792 |
| rs140738978 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139530 | AATTTAAGGTATATT[G/T]TGTTCCATGGGTCTT | 114792 |
| rs140769507 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017042 | TTTATAAATTACCCA[G/T]TCTCAGGTATTTCTT | 114792 |
| rs140772697 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909400 | CAGTTTTTAGATTCA[A/G]CAATCTTGTGTGATT | 114792 |
| rs140803627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087554 | CCCATGTCTTAAAGA[A/G]GAAGTGTGAAGCAAA | 114792 |
| rs140814217 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082474 | GAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 114792 |
| rs140814433 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997787 | CTGCTTAAGCCTCTC[A/G]AGTAGCTGAGACTAC | 114792 |
| rs140833463 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964563 | GAGGCTGAGGCAGGA[C/G]AATGGCGTGAACCCG | 114792 |
| rs140836247 | in-del | -/C | 0.130694 | 0.219696 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006076 | CTTTGTTAGTTTTTT[-/C]CCCTCAATGATCTAA | 114792 |
| rs140891756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072153 | CTAGAATCTCCCATC[C/T]CCTTGAGCCCCACAT | 114792 |
| rs140910721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050414 | GTGCAAAAATGGCTT[C/G]AGAGAGCATGGAGGT | 114792 |
| rs140920833 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953220 | TCCAAGAATCTATCA[A/G]TAATGTATGTGAGAA | 114792 |
| rs140922827 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990433 | GGTAAGTTCTTGCTC[A/C]ACCACGTGGCTCCTC | 114792 |
| rs140940489 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931177 | GGATTAAAATCTTCC[C/T]GAACAGAATACTTTC | 114792 |
| rs140961356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033913 | TGAATTTTGAGTTCC[C/T]TAAATATTTTGGATA | 114792 |
| rs141010099 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956733 | CTGGGAAAAAAGCTC[A/T]TTTAATTCTTATAAT | 114792 |
| rs141017430 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911437 | TCTTTACAAACAATA[A/G]GCTTCTCAATCAGCT | 114792 |
| rs141026525 | snp | A/G | 4.94474e-05 | 0.00497205 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085242 | CTCTGAACTCCTGAA[A/G]AGCCGCCCAGAAGAA | 114792 |
| rs141029871 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981366 | TTGTAGTCTTTGAGG[G/T]TTTTTTTGTATTTCT | 114792 |
| rs141054915 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040478 | TTCTCAAATTCAAGT[A/G]GGCATGAGAGTCACC | 114792 |
| rs141063126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120718 | GTTGTCCCTGGAGGC[A/G]GCCATGATGTGAGGA | 114792 |
| rs141075853 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018453 | AAAAAATTATCTGGG[A/C]GTGTTGGCGCACTCC | 114792 |
| rs141076192 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068884 | TTTTTTATTCATGGA[C/T]ATTAATTTGTCATTA | 114792 |
| rs141093159 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989069 | TGTAACAAACCTGCA[C/T]GTTGTGCACATGTAC | 114792 |
| rs141103064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093666 | CAATAAAGTCGTACA[A/G]GAAAGTGTTGCTGAG | 114792 |
| rs141127693 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978442 | GAATAATGGCCTCCA[G/T]CTCCATCCATGTTGC | 114792 |
| rs141172422 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023060 | ATCATGGGGGAAACC[A/G]TCTCCACAATCCAAT | 114792 |
| rs141173070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932840 | GCTTCCAAAGTGCTG[A/G]AATTAGAGATCTGAG | 114792 |
| rs141217046 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983193 | ATGTTTATTGATTTG[C/T]ATATGTTGAACTAGC | 114792 |
| rs141229097 | snp | A/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899620 | GCCTGATCCTGGCCC[A/T]GTGCTGCTCAGGCCC | 114792 |
| rs141229379 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920572 | AAAACACACACAATT[-/AC]ACACACACACACACA | 114792 |
| rs141247610 | in-del | -/A | 0.029116 | 0.117091 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945089 | CTCTTGTTATAAACT[-/A]CTTAAAATATTTTTG | 114792 |
| rs141260212 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117180 | AATACAGGTATAGTT[C/T]ACCCTGCCTATCACT | 114792 |
| rs141267259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903769 | AATTCAACACCCATT[A/G]CTAAAAATACATTTA | 114792 |
| rs141299776 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969517 | CCAATCCAGATGAAC[C/T]GATCTATTCATATTT | 114792 |
| rs141300389 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121836 | AAGAGGAGAGAAGAT[G/T]GTTAAAGCTACGCCA | 114792 |
| rs141326473 | snp | C/T | 0.191775 | 0.243125 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056326 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 114792 |
| rs141345018 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906584 | TAAGGTGCTGTTATT[C/G]TCATCCATGTGGGAG | 114792 |
| rs141371850 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004830 | GGAAAAAGCCTATTT[C/G]ATCGTAGTGCATTAG | 114792 |
| rs141372789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060445 | TGTCCCTACTCCCAC[A/C]GCTCAGTCCCAGCTC | 114792 |
| rs141373648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095612 | TGACCTATACACAAA[A/G]TGCCTTCTAGGCAGA | 114792 |
| rs141408661 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008786 | TCCAGCCTGGCCTCT[A/G]TGTCTTCCTTCCATC | 114792 |
| rs141426812 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937095 | AACTTACATATCATT[A/G]AAGTTCACCCATTGT | 114792 |
| rs141439292 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990111 | GCCATTTCAGCCTGG[G/T]TAAGAACACTTGCTG | 114792 |
| rs141455143 | in-del | -/AACC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968953 | GATTGTTTGAGAAAG[-/AACC]CCACAGCCACAAAAA | 114792 |
| rs141459615 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955464 | GTTTTTTCATCTCTT[C/T]ACTATAGTTTCAGTG | 114792 |
| rs141481638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062508 | ATAAGATGAGTGTTG[A/G]TATTTTTGCCACATG | 114792 |
| rs141498325 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040855 | CTCTTCCCCTTCCCT[C/T]GGCACTTCTCCTTTC | 114792 |
| rs141500475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048408 | TCTGACCCAGAGAAT[C/G]CTTCAATACGATCTT | 114792 |
| rs141509262 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137022 | TTTTTTCCGGTATCA[A/G]TTTTCTTCTCTGTAA | 114792 |
| rs141543254 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927065 | GTTTTTCAATAAACA[A/G]GTTCAAAAATTTTTT | 114792 |
| rs141548035 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995237 | TTCCTGGTCATGTTC[C/T]GCCTAGGTGTTACGG | 114792 |
| rs141554500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111954 | TAGTCTCTGACATTT[A/G]GCTGCTGCTTCTCCT | 114792 |
| rs141558875 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000979 | GACATTCTGGAAAAG[A/G]CAAAACTATGGAGAC | 114792 |
| rs141573368 | snp | A/G | 0.00844532 | 0.0644309 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085311 | GAAGAGCGACCGCCT[A/G]ACCTCCCTGAGTGAA | 114792 |
| rs141580679 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950620 | TGAGTGAGTGAGTGA[A/G]TGAGTGAATGAGTGA | 114792 |
| rs141592454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046748 | TCTTACTATGGAGTC[A/G]ACATTAACATTAAGC | 114792 |
| rs141607471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006417 | TATTGCATGTGAGAT[A/G]GGCCTCTTGAAGCGA | 114792 |
| rs141609687 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900401 | AAAAATTTGAGATTA[C/T]GGTAAGACTCATGTT | 114792 |
| rs141628948 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126341 | CTTACTATGCTGTTT[C/T]ATGTTTTTTTTTTTT | 114792 |
| rs141641259 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090212 | GAATGGATAATAAGA[C/T]ATCCTACTATTCCTA | 114792 |
| rs141644047 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974913 | CGGTATTTTTACTCA[C/G]CTTTGAGATGGATCT | 114792 |
| rs141644345 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924990 | GCCTGCGCTGCCGTC[C/T]CTGGCACCTAACCCA | 114792 |
| rs141651600 | snp | C/G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005574 | TAGGTGTGATATTAG[C/G/T]TTGTTAATTTGAGAT | 114792 |
| rs141653582 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967663 | TGAGGACCCAGCTAT[G/T]AATAAAACAGATAAG | 114792 |
| rs141682218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930065 | AGAAGCAGGCTACCC[A/C]CTCCCTTCCCCACCC | 114792 |
| rs141709046 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940622 | GAACCATACTATAGC[C/G]CTGCTTAAGCAGCCC | 114792 |
| rs141713956 | in-del | -/T | 0.252983 | 0.249982 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946181 | TATTTAGGAAAAAAA[-/T]ATTTTAAATATTTTG | 114792 |
| rs141715798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013321 | CTCTATTGTTAAGTT[C/G]CCACATTATATGAGG | 114792 |
| rs141777180 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950125 | TGAGTTTTGATATCT[C/G]AAAGTTGTTAAAATT | 114792 |
| rs141782753 | in-del | -/AAAC | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039823 | AAAAACAAACAAACA[-/AAAC]AACAAACAAAAAACA | 114792 |
| rs141798996 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142357 | CCATTTGGTAATTTA[C/T]AATGCAGGTTATCAC | 114792 |
| rs141860653 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959569 | ATCATTTTGAATTAG[A/G]GCCCACCCAGTAACC | 114792 |
| rs141863708 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083261 | TGGGTGCGATGGCAC[A/G]CGCCTGTGGTCCCAG | 114792 |
| rs141865860 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035051 | TAAAAGCGGTCTCTC[A/G]TCTTCTCTTGCCATC | 114792 |
| rs141868454 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131863 | CTCTCTGAGTTTTAG[C/T]GGTACCTTAGGCCCT | 114792 |
| rs141879523 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912410 | ACTCTCCCCTTGCAT[A/C]TTTAGTCAATAAGTT | 114792 |
| rs141902371 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019557 | ATCCCTGAAAAGGCT[A/G]GCAGGTGAAGTCGGT | 114792 |
| rs141903253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102087 | CTTGTTTTGCTGAGT[A/G]TCAGTATGTTGATAA | 114792 |
| rs141919637 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061270 | CACCCAAGCAGGTGA[A/G]CGTCACTGGGGGTAG | 114792 |
| rs141919658 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040190 | TATAAAGTTAGCTAA[A/C]CTGCAGAATCTCAGG | 114792 |
| rs141921333 | snp | C/T | 0.000296663 | 0.0121755 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114383 | GGCAGAAATGAACTG[C/T]GCCAGGTTCTGCCTA | 114792 |
| rs141925909 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110048 | ATCTCCCCAGAAATA[A/G]TTGGAACCCCGTGTC | 114792 |
| rs141965009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071988 | GTCCTTTCTATTTCT[C/T]GTCTCTATAATGTAC | 114792 |
| rs141968097 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967160 | GTTCTAGGATCAAGC[A/G]CAAAGCAGGGGCTTA | 114792 |
| rs141982180 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025405 | CATATCAAATCATTC[A/G]TATCACTTTATAATC | 114792 |
| rs142001175 | snp | A/T | 0.159622 | 0.233092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984915 | TTTGATCCTGTCATT[A/T]TGATCTTAGCTGGTT | 114792 |
| rs142007783 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064129 | ATGAAGCTTACTGTT[A/G]TAGGACTTAGAAGTA | 114792 |
| rs142041286 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111462 | TAAACTTCACTCACT[C/T]GAACCCGCTGCACCC | 114792 |
| rs142055706 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028267 | TGCTGCTATTCCAGG[G/T]ACCACACCTTAAGTA | 114792 |
| rs142091875 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119479 | CTACAGGGATATCAA[A/G]GTCCAAAATATTTCC | 114792 |
| rs142095389 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971608 | AAAAGGTCATCTTAC[C/T]GTTCAGGGAGTCTGG | 114792 |
| rs142106206 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914979 | TAGGACTATAGGCAC[A/G]GACCATTGCGCCCGG | 114792 |
| rs142116315 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022174 | ATTTCTGCTCAAACC[C/G]TATGACGGTTTCTAC | 114792 |
| rs142125373 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988845 | CATTCTCAGCAAACT[A/G]TTGCAAGGACAAAAA | 114792 |
| rs142133609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103856 | GGTACTAGATTAATT[C/T]TGGTTGCCTCTACCA | 114792 |
| rs142153995 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086882 | AAAGATTTGGAATGA[A/G]TCCTGCATTTAATTT | 114792 |
| rs142179982 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968838 | CCTCTCAAAGTAGTG[A/G]CATTATTATTTCCTC | 114792 |
| rs142185739 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044518 | AATAATGCTAGTCTC[A/G]TAAAATGAATTTGAA | 114792 |
| rs142191535 | in-del | -/T | 0.137527 | 0.223271 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014393 | TATATAACAAATTGG[-/T]TATATAGTATGTCTA | 114792 |
| rs142226906 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922740 | TAATGGTACCTAAGA[A/G]AGAAATGGTGCCTAA | 114792 |
| rs142248266 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946911 | CATAAAATGAGCTGT[A/G]AATTGTAGAAAAATA | 114792 |
| rs142267749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980780 | AGTCAGCTGTGAATC[C/T]ATTTGGTCCTGGGCA | 114792 |
| rs142271617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056040 | CTAATTAAATACTGT[C/T]ATATGTGACCTCACA | 114792 |
| rs142277010 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105836 | GCATTGCTTTAAAAG[A/T]TTTGATCACTCATCT | 114792 |
| rs142287245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934242 | AGATTACTGGATCTT[C/G]TATACTTACTGTGTG | 114792 |
| rs142322831 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133866 | AGTTGGAAAGACTGT[A/T]TTTTTCTTAGCATAC | 114792 |
| rs142333686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091440 | CTGTGGGGTACTACT[A/G]TTGCCTGCCATATGA | 114792 |
| rs142355704 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083090 | GAGCTTGTTGAGCTC[C/T]TAAATTTGTACTTGG | 114792 |
| rs142369456 | snp | A/G | 0.0126979 | 0.078662 | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96999511 | TCACCATATTTGATG[A/G]AATTTTGAAGTGAAC | 114792 |
| rs142382603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049001 | CCCTGAGGCACCTCC[A/G]CTGTGCCTTGCACTC | 114792 |
| rs142390286 | in-del | -/A | 0.154661 | 0.231107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951135 | TATTATTAATAATGG[-/A]AAAAATATACATGGG | 114792 |
| rs142407133 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965093 | GTGAGAAGAACATGT[A/G]TTATTTGTTTTTCTG | 114792 |
| rs142409412 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003157 | TAACCTTGCCAGCAT[C/T]TGTTATTTTCTGACT | 114792 |
| rs142438057 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927864 | AAACACACTGCTCCT[A/G]GCAGCGTCCACTTTT | 114792 |
| rs142465688 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096893 | TTTTATCTTCTCATC[A/T]TTTAACAGCAGCAGA | 114792 |
| rs142475481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051999 | TCAACCTCAACTGTC[A/T]GTCCTTAATATAAAA | 114792 |
| rs142479378 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038332 | TCACTAGCAAAAAAA[-/A]AAAAATCCAATTTAA | 114792 |
| rs142525654 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991497 | TATGGGTTGTCTCTG[A/G]GGATTTCCTCCCCAA | 114792 |
| rs142530323 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907245 | CAGGTACTCTTCATC[C/T]AGTATCCATAATTAC | 114792 |
| rs142543804 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076842 | TTTAAATATTAAATA[A/G]ATGTATTAATATTTA | 114792 |
| rs142567696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063784 | TGGTCCAGAGACCAG[A/G]TTCAGGAAGCACTGG | 114792 |
| rs142572799 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957772 | TATTTTAATTTGGTT[C/G]CCAAGGTCTCCAGCT | 114792 |
| rs142614641 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132218 | GCTAGGGGCATGGCT[C/T]TGCTTTATTGGCTTC | 114792 |
| rs142633194 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997526 | GCCCAATGGGGAGAA[C/T]TGCCTGAGCTCAGGA | 114792 |
| rs142640445 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128859 | CAGGCTTTGCAAACC[A/G]GATGGCGTCCATAGT | 114792 |
| rs142642710 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929385 | GGGCTTTTTGGTGAC[A/C]GCAGAGATAGATGTG | 114792 |
| rs142643932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115563 | TGTTTTCTCTACACC[C/T]ACAGACCCATCACAC | 114792 |
| rs142681380 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943741 | TCCAGTTAAACACTT[C/T]GAGCTTCCTGCTTTT | 114792 |
| rs142683654 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086132 | TTACTTGTAGGGTGC[A/C]ATGCCTCCAAGATTT | 114792 |
| rs142744489 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111600 | TGGGGAGTGCCTGTA[G/T]CCCCCAAAGCTCCAG | 114792 |
| rs142747729 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902886 | CAGGTTTGTCAAAGA[G/T]CAAATGATCATAGGT | 114792 |
| rs142788796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008232 | CTGTGTGTTTCAGCC[A/G]GTTCCAGTGCACTGG | 114792 |
| rs142796254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065521 | AGTCTCTTGGACTTT[A/G]TAGAGTGTTACTAAC | 114792 |
| rs142800664 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058655 | GTTTGTAAGAAATCT[A/G]TTGTTTTTCTGATAA | 114792 |
| rs142820178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061983 | CTGGTAGGGTTTCTT[C/T]CTCCAACCCTTTAAG | 114792 |
| rs142821972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007755 | TTTTATGAGGCCAAG[G/T]CTCAGCTCAGCACTC | 114792 |
| rs142824101 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975083 | GTCCATAGCTGTCTG[C/T]AAAGTGAAAGTTTGC | 114792 |
| rs142839042 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987187 | ATTGATTTTTTGAAG[G/T]GTTTTTTGAGTCTCT | 114792 |
| rs142840034 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945244 | AATTGTGGATAGTGC[A/G]TGGCAGGGATAATGC | 114792 |
| rs142854913 | snp | A/G | 0.00541 | 0.0517275 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085332 | CCTGAGTGAAGAGCA[A/G]ATCTGGCAGGTAAGG | 114792 |
| rs142874527 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069905 | AGTAATACTACAATG[A/T]CTTATAGGAGGTTAT | 114792 |
| rs142875612 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939849 | AGTAATCAGAATAGG[A/T]GGGCACTGGAGTCCA | 114792 |
| rs142909118 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012319 | AAGATAGAAGAAAGA[A/G]TCAGCAGAGTCACAG | 114792 |
| rs142910156 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000797 | GAAGATGTTACTCAG[C/T]AGGTGAATAGGTAAA | 114792 |
| rs142924480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932374 | GGTATTCAAGATCAC[C/T]TACAGATGGGGCCTC | 114792 |
| rs142927559 | in-del | -/A | 0.146985 | 0.227789 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938272 | ATAATTCCATAGTGG[-/A]AAAAAAAAACAAATG | 114792 |
| rs142963790 | snp | A/C | 1.65348e-05 | 0.00287526 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896817 | AGCTTTTCATCTTTA[A/C]GAGCAATCTCTCCTT | 114792 |
| rs142971504 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913005 | TTGTCTGAATGAATA[A/T]AGATGCAAAATTATT | 114792 |
| rs142973120 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966857 | TGTTAAAGGAGCATT[G/T]TGTCAGAACGTTTTA | 114792 |
| rs142983030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952355 | CCAGAAATATGCCAT[A/G]GGAACTTAACTCTTG | 114792 |
| rs142987164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025969 | GCTATAGGGAGGCCC[C/T]AGAAGAAAAAACTAT | 114792 |
| rs143006622 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904693 | GAAAGAATAGCCAAT[A/G]GATTTTAGAAAAACA | 114792 |
| rs143012769 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919286 | CAGTTGCTTAAAACA[A/G]AAGCAAAAACCTGTA | 114792 |
| rs143015023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011548 | AAACTATTAAATTAT[A/G]AAATTGTTGAATTTC | 114792 |
| rs143020993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094939 | AGTGATGGATGGTGC[A/G]TTAAAGTTTAAACGT | 114792 |
| rs143047400 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983141 | TATTGAGATAATCAT[A/G]TGGTTTTTGTCATTG | 114792 |
| rs143113677 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925241 | TCTTCCCTCCCCCTG[A/G]GCCCAATATGTACTG | 114792 |
| rs143122645 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958389 | TGACATCTGAAACCT[A/G]CAGGATGAATAGGGG | 114792 |
| rs143124588 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997022 | CATTGTGATGGATGG[C/T]GATGGGGAGGAAAGA | 114792 |
| rs143142111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080895 | GGGAGATGTGCTGTA[G/T]AGGATATTCAGATGA | 114792 |
| rs143169243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073575 | AAAGTCTTTCATCTC[C/T]AGTTCTAGTGCATGG | 114792 |
| rs143188614 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027206 | GATAACAGATCTTAT[A/G]GATGACATTGTGAAT | 114792 |
| rs143202506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076117 | AGAGTATATTATAGT[A/G]ATACATACTTGCTTA | 114792 |
| rs143233318 | snp | A/G | 0.196771 | 0.244268 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988763 | TATACACCATGGAAT[A/G]CTATGCAACCATAAA | 114792 |
| rs143243285 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030268 | TTTTTGTCAGTTTTG[C/T]GTCGTAAGGTACCAC | 114792 |
| rs143257709 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079288 | ACCCACCAGGGGACA[A/T]CACCGAGGCCAAGAC | 114792 |
| rs143275508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121925 | AGAGCACAGCAAAGC[A/T]GGGACATGAAAGACA | 114792 |
| rs143292549 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990046 | CTTTCTCCTGAATTG[C/T]GATGATCTTCATTCT | 114792 |
| rs143302428 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961700 | GGAAAGATGATTGGT[G/T]AGTCGGAAAGGTGAG | 114792 |
| rs143302850 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919087 | ACCTAGACTTGACCA[A/G]TTAGATTCTCCTGGG | 114792 |
| rs143336807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089908 | CCAAAAAATTTGCTG[A/G]CTATGTGAGTGGCGT | 114792 |
| rs143338505 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983206 | TGCATATGTTGAACT[A/C]GCCTTGCATCCCAGG | 114792 |
| rs143367426 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120947 | AAAGCTACTCTAGTA[C/T]TGAACTGAGGTGGAA | 114792 |
| rs143375842 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971149 | TTATTGGTAGTCTTA[C/G]TTAAAAACTACTGCA | 114792 |
| rs143379221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047320 | GACACTGCTTGAATA[C/G]ACCTTGGGATGCAGT | 114792 |
| rs143390415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935845 | TATTTAAATCTCTAT[G/T]CAATAATATGACCTT | 114792 |
| rs143395074 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926181 | AGTAAAGATCCACTG[G/T]CATTCAAGAATTAAT | 114792 |
| rs143436572 | snp | A/G | 0.031825 | 0.122064 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056967 | TGTAAATGAATAAGC[A/G]TAGCTATGTTATAAT | 114792 |
| rs143437172 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127031 | ACAATTTAGTGAAGG[A/G]CAAGAATTTTCCATA | 114792 |
| rs143439718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949164 | TAGAATGTAAGTTCT[C/G]TGAAAATAGGGACAT | 114792 |
| rs143450022 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140775 | ACTAACTTCATATAT[C/T]GTTATACACAAAACA | 114792 |
| rs143460605 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939519 | CTTTGACCTGCTCTG[A/G]AGGTTGATGAGGAAG | 114792 |
| rs143481422 | snp | A/G | 3.30104e-05 | 0.00406252 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114318 | CCATGAAAAACTGCC[A/G]GGAGCATTTTGTGCT | 114792 |
| rs143481473 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005703 | CTCATTAGTTTCAAA[G/T]AATTTCTTGATTTAT | 114792 |
| rs143493827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077889 | AGCATACGATGCGAA[A/G]TCTACTTTTTACTAG | 114792 |
| rs143508329 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992921 | GTTTCCACTTAAGCT[A/G]TGTGCTCTGCTGGAT | 114792 |
| rs143515631 | in-del | -/TTTG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003365 | TTTTTGCTTGTTAAT[-/TTTG]TTAAGTTCCCTATAG | 114792 |
| rs143576726 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020123 | GATTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 114792 |
| rs143578311 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055816 | AAAAAAAAAAAAAAA[A/C]AAAAAACCCCTTCTT | 114792 |
| rs143607886 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096050 | CAAATTTTGCTAAAT[A/G]TTGCACGGAAAATTC | 114792 |
| rs143609338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068931 | CACTTTTATGTGAAA[A/G]ACGTGACCTGCAAGA | 114792 |
| rs143631690 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897113 | CATTGTTTGTAGAGA[C/T]GGGGTTTAGCCATGT | 114792 |
| rs143671789 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983363 | TGTTGTGTCTCTGCC[A/G]GGCTTTGGTATCAGG | 114792 |
| rs143684567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078742 | AAGGGTGCCTCATCT[A/G]GTTTTAAGAATGTCA | 114792 |
| rs143710235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959499 | CTCCCTGTGTCCTCA[C/T]GCGGTCTTTCATTTG | 114792 |
| rs143715977 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982478 | CTTGAAGACAGCACA[C/T]CATTGGGTCTTTCCT | 114792 |
| rs143750282 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057488 | CGCCCGGCCGAGTAT[A/C]TTTTTATATGCTTAT | 114792 |
| rs143758559 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942929 | CCTCTCTCTTGCCCA[C/T]ATGCCACAGTTAAAA | 114792 |
| rs143761576 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016643 | ATGTTGGATTGAGTT[A/G]AGACTTTGGGGGATT | 114792 |
| rs143769796 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134698 | CAGATTAGCTCAAGG[A/C]ATAGAAAATTAGTGG | 114792 |
| rs143774121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060561 | TCCCATTCTCCTCCT[C/G]TTTCACCGGATTCTG | 114792 |
| rs143785845 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994666 | TGAATGATTAGTTGC[A/G]TGCAAAGTACTATGA | 114792 |
| rs143799849 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000399 | ATGGGCATTTTTTGA[C/G]AGGAAGTCTTTCTTG | 114792 |
| rs143821698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966867 | GCATTGTGTCAGAAC[A/G]TTTTATGTGGACAGT | 114792 |
| rs143865018 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063148 | ATTAAAACAGATAGT[A/G]TGAGTGGACAAAGGA | 114792 |
| rs143910398 | in-del | -/GGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991107 | CTCTCCTTATGGCGG[-/GGT]TTTTGGTGCTGGGAG | 114792 |
| rs143918531 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942119 | TGAAGCACATGTGTT[G/T]CTCTAACATTCTCCT | 114792 |
| rs143929658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080461 | ACCAGGGACACACAA[A/G]GCATGAGACACAATC | 114792 |
| rs143931228 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977946 | AATTATACATTTCAC[A/G]CACCCTCACTCACAT | 114792 |
| rs143957191 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962636 | GGAGCAAATCACTAC[A/G]TGATTCATATTTGTA | 114792 |
| rs143959636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968484 | ATACAGCACATGGAG[A/G]CCATGGTGTCTGTCT | 114792 |
| rs143961560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915560 | AGGAAAGAGCACTGA[A/T]CTTGGGAGATAAAAA | 114792 |
| rs143969027 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118746 | CTTGTGCTGCATTTC[A/T]TATCCATGATGAGAT | 114792 |
| rs143979881 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037726 | AATAACCAAAGCCAC[C/T]CTGAGCAAAAAGAAC | 114792 |
| rs143981124 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037614 | ATACTATCCAAAGTA[A/G]TTTACAGATTCAATG | 114792 |
| rs144017841 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019115 | CCTATCATATACTTG[C/G]AATTGTAAAAAATAC | 114792 |
| rs144019025 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987702 | ACCTGACTTCAAACT[A/T]TACTGCAAGGCTACA | 114792 |
| rs144021070 | snp | A/G | 0.000510704 | 0.0159716 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041533 | AAGTGGAGCTGATGA[A/G]GTTAATTTGCACGGT | 114792 |
| rs144035028 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124699 | TGGGTGGAGCTTTGC[C/T]CTCGGTTCCATTTCA | 114792 |
| rs144038292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944809 | CCTTGCTGTACTTGG[A/G]AAAATAAAAGAAATA | 114792 |
| rs144042130 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138901 | GCTTATAAATATACA[C/T]GTATGTATATATGTA | 114792 |
| rs144071192 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896487 | CCTACAAATTCTGAA[A/G]TACTATGAAATAATT | 114792 |
| rs144072099 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919974 | ACCAATCAACCAACC[G/T]AATTTGCTTCTTGAT | 114792 |
| rs144093577 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001331 | GAACCTAAAACTGGT[C/T]TAAAACATACATTTT | 114792 |
| rs144105759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086416 | TTGCTTCCACCAGAG[A/G]GAATTAAAGAGCTGC | 114792 |
| rs144113690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990348 | TTTTATGGGGGTGGG[A/G]GTTATGTTAGCAAGT | 114792 |
| rs144128487 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082368 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCCGAGG | 114792 |
| rs144143475 | in-del | -/T | 0.0189856 | 0.0955633 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924045 | ACAGTAATCACACCC[-/T]TTTCTCATTTCTCAG | 114792 |
| rs144151866 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040136 | TGAACTAAATACCAC[A/G]TAGCATAGTGAGGTT | 114792 |
| rs144161772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964039 | TTTGTGATAAATGCA[A/G]TTCTATCTCTTGAGA | 114792 |
| rs144182043 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984126 | TTATTTCTGCCTTCA[C/T]TTCGTTATATGCCCA | 114792 |
| rs144182652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936995 | CTGCCCACCACCCCA[A/G]CCCCTTCACTCTCAA | 114792 |
| rs144196910 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114746 | TTCAAGGTGGAAATT[A/G]TTGGTCCATCACAAC | 114792 |
| rs144222190 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985808 | TTTAACTTCTTTGCC[A/G]TGGGTACGAACTTCC | 114792 |
| rs144231031 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908050 | CTCTGAGGCAGAAGC[A/G]TGCTTGACATTGTAC | 114792 |
| rs144261428 | snp | A/T | 0.000131811 | 0.00811715 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139220 | TTCCTTCCAGCTCCA[A/T]ATTTTACATGCCCTA | 114792 |
| rs144271389 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068463 | TTAAAGCAAAAATCA[C/G]AAAAAATAATGAAAA | 114792 |
| rs144366035 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933347 | TTGCTTCAGAATTCC[A/G]TTGCCATCCATTCTT | 114792 |
| rs144370224 | snp | A/G | 0.000214283 | 0.0103487 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085207 | GAGAAGGCAGTGATC[A/G]ATTTCTTAGTGAAAC | 114792 |
| rs144394948 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098120 | CCTAATCTTGCAGCT[A/G]TTTGAAGTATAGGCT | 114792 |
| rs144398167 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002476 | TTTTTGTTTATTTAT[C/T]ATTTTTTGCACTTTT | 114792 |
| rs144413719 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029895 | TGCCTCATGGCCATT[A/G]TAAACATCATTAATT | 114792 |
| rs144459928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936241 | ATTTTAAATAGACAT[A/G]TCTACATTTTGCATG | 114792 |
| rs144461175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935539 | TAACTGTGAAACCGC[A/G]TCTATCATCAATTGA | 114792 |
| rs144470753 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042898 | GTTGGGGTCATGTTG[A/G]TTGATTCTTCGTGAA | 114792 |
| rs144476167 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125433 | AGATAAGGTTAAACA[A/G]AGAAAGAAGACTTTA | 114792 |
| rs144513859 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059825 | ATTTAACAGCTATTT[A/G/T]TGCTGTTGTATCCAG | 114792 |
| rs144535289 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983795 | ATTAGTCTTGCTAGC[A/G/T]GTCTATCAATTTTGT | 114792 |
| rs144540420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062057 | TTATGTTATAATGAG[C/T]GGAAGGAAAAAACTA | 114792 |
| rs144578410 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049389 | GCATCTACAATGAGG[A/G]TATGCTGAACAAAGG | 114792 |
| rs144581195 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939945 | GAGAAATTGCCTAAG[A/G]ACAACTCAGGAGGTA | 114792 |
| rs144587464 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973869 | CTGGGATTAAGGTGC[A/G]CGCCACCATGCCTGG | 114792 |
| rs144603903 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041564 | GTGACCAGCCTTGGC[C/T]TAAAGCAGGCTCTGG | 114792 |
| rs144611636 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139605 | ACAACATAACACTGT[C/T]AGTAAGGCAATTTAT | 114792 |
| rs144627695 | snp | A/G | 1.64852e-05 | 0.00287094 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897709 | GGTAGAGGGGTGTCT[A/G]GGAGCGACAGAGGGC | 114792 |
| rs144647634 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052526 | TCTGTGTAAACAAAT[A/G]TTTCACTTCTTTGCA | 114792 |
| rs144652711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003283 | ATATGCTTGTTAGCA[A/G]TATGTATGTCTTCTT | 114792 |
| rs144674698 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087893 | TGTTCCTTACCCAAG[C/G]CCTTTCCTTGACAAA | 114792 |
| rs144688152 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059282 | AGGTATTGCCTGAGT[A/G]TGGAGACTAGTAGAT | 114792 |
| rs144702823 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140405 | TATGTCAATCTTGAG[C/T]GCTTGTGGAATTCTT | 114792 |
| rs144712671 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056351 | ACCTCGTGATCCTCC[C/T]GCCTTGGCCTCCCAA | 114792 |
| rs144716384 | in-del | -/TC | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951857 | ATTATTTTAGCTGTT[-/TC]TCTTTAGATAGCAGC | 114792 |
| rs144743903 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97008069 | CCTCCTCATGCAGGT[A/G]GTTGTGGTGGTGGTG | 114792 |
| rs144765501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911442 | ACAAACAATAAGCTT[C/T]TCAATCAGCTGTCTA | 114792 |
| rs144818464 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989276 | CTCCCTTAAGTGCCT[A/G]TGTTAAGCCAGGTCT | 114792 |
| rs144860798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987517 | AATATCATGAAAATG[A/G]CCATACTGCCTGAAG | 114792 |
| rs144864975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070996 | CACCTTTCTGCTCCT[C/T]ATTCCATCAGTTACG | 114792 |
| rs144869608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903221 | TTTTGGAAAGAATAC[A/G]ATCATAAATATGGAG | 114792 |
| rs144869700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956734 | TGGGAAAAAAGCTCA[C/T]TTAATTCTTATAATG | 114792 |
| rs144886498 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953900 | GTTATCAACAATTCA[A/G]TCCTCAAACTCTCCT | 114792 |
| rs144888937 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991386 | CTCCGTATGGTGGCT[-/G]GGTGTGCTAGGGATG | 114792 |
| rs144907299 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954866 | GTTTCTCTATTGTCA[A/G]CTGTCTTAGCCAGCT | 114792 |
| rs144918833 | snp | A/G | 0.000115322 | 0.00759261 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114047 | ATCATTGGTGGGAAA[A/G]AGCGCGAGGTCTGCA | 114792 |
| rs144995842 | in-del | -/TATTTATA | 0.376592 | 0.215579 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953786 | TGACAATCTAAATGT[-/TATTTATA]TAATCAAACCATGAT | 114792 |
| rs145029051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070464 | CAATTAATTTTTTTC[A/G]TATGCTATTATGTTG | 114792 |
| rs145034617 | snp | C/T | 8.23771e-05 | 0.0064173 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113993 | CCTGTCTGGCAGACT[C/T]GCAGGACCAAACCAC | 114792 |
| rs145065556 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027015 | AAAAATACAAAAACC[A/T]GCTGGGCGTGGTGGC | 114792 |
| rs145076998 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073946 | TGCACATCAAGGGGC[A/C]TGTGCCACAGGCCCT | 114792 |
| rs145082736 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109773 | CATGGATATTTATCT[A/G]ATGTCTCTAGTGCTG | 114792 |
| rs145093164 | in-del | -/C | 0.0685596 | 0.171987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102189 | ATCAAGTCCTGTATT[-/C]TTTTCCTTGTGTCAG | 114792 |
| rs145096480 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004834 | AAAGCCTATTTGATC[A/G]TAGTGCATTAGCTTT | 114792 |
| rs145105647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934750 | ATAAAACTAAATACT[A/T]TTTAATTTTATACTT | 114792 |
| rs145124773 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072777 | TGCCTGATCAATCTA[C/T]TCAGTTGGAATTATA | 114792 |
| rs145125268 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937837 | CTAATATCTTTAGAG[A/T]TGTGGCTTCCATCAT | 114792 |
| rs145130949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968539 | ATTTCTGGCTACCAG[A/G]ATCAGTGTGCATACT | 114792 |
| rs145132059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030710 | TTTCTAAATGTCTAG[C/T]TTTGAACTCACTTGT | 114792 |
| rs145201887 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014235 | GGGAGGCGGAGCTTG[C/T]AGTGAGCCGAAATCG | 114792 |
| rs145206245 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983444 | TGATTGGAATAGTTT[C/T]AGAAGGAATGGTACC | 114792 |
| rs145222259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980484 | ATTTGCATATAGTGA[A/G]CCAACCTTATATTTC | 114792 |
| rs145268836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978580 | TCCATGTCTTTGCTA[A/T]TGTGAATAGCGCTAC | 114792 |
| rs145273221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040744 | TGTCAAGGGAGAGAC[C/T]AGATGGAGGGTAATT | 114792 |
| rs145287913 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965090 | GAAGTGAGAAGAACA[C/T]GTGTTATTTGTTTTT | 114792 |
| rs145294965 | in-del | -/T | 0.094964 | 0.196122 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925958 | GGTTTTTGCTTTTTG[-/T]GTTTTTTTTCTGATG | 114792 |
| rs145317046 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091048 | GTGCAACATAGTGAG[A/G]CCCCTGTCTCTACGA | 114792 |
| rs145361642 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139912 | TACAGTGCTTCAGTT[A/T]TCCCACCTTTTAAGG | 114792 |
| rs145361690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021713 | ACAAATTTATATTTC[C/T]GAATTGGACTTCCCC | 114792 |
| rs145392673 | snp | A/G/T | 0.00215574 | 0.0327605 | upstream-variant-2KB, missense, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897762 | CCGCTCGGTTCTCTA[A/G/T]GTTGAAATTCCTGAT | 114792 |
| rs145396413 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089032 | CTAGCATAGGGAGAA[A/G]GTATGGCTCTCCACC | 114792 |
| rs145399961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132994 | GTAATATATATTGGA[A/C]ACTGGGAAACTGGGA | 114792 |
| rs145412269 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050015 | AGTCTGTTCTCCTTT[A/G]TTAAATTTCTCTGTG | 114792 |
| rs145429540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028017 | GTTTTACTAATATTT[A/C]TCCAGCAAGGGACAG | 114792 |
| rs145443237 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955285 | TATTCCTTGATGCAA[A/G]TTGAGTTTTTTCTTT | 114792 |
| rs145449423 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910064 | CTGGACTGCAGCTCT[A/G]TTATGAGGTGTTGCT | 114792 |
| rs145452086 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998025 | CATAAAGGATAAATG[A/G]CAGCATAACATTGAC | 114792 |
| rs145461036 | snp | A/T | 0.000181451 | 0.00952326 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139152 | GAGAAGGCAAAGAAG[A/T]AGTATTCTATGGGCC | 114792 |
| rs145481564 | snp | C/T | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897802 | CACTAGTGCTCCCAT[C/T]TCCTCATAACATTAT | 114792 |
| rs145484507 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906819 | GAGCTTTTGATTCCA[C/T]AGAAGCTCAGGATGT | 114792 |
| rs145506060 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909193 | CAAGTGCCTATCCTT[C/T]GGTAGGGTTAGAGAA | 114792 |
| rs145523124 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033800 | GCATCTTTTTATATA[C/T]CTGTTGCCCATTTGT | 114792 |
| rs145552576 | snp | A/G/T | 0.000116557 | 0.00763314 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967066 | CAGCTGGAAAATGCC[A/G/T]TCTGAACGCTGCCTC | 114792 |
| rs145583217 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910613 | GCTTGTTTCTGAGAA[A/T]AAAATACAAGTTTAA | 114792 |
| rs145600290 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914327 | GACAGGAAACTAATA[A/C]CAAAAATCCTCTGTA | 114792 |
| rs145638017 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928542 | GTAGTACTGATTCTT[C/T]TAAAGACTGAACATA | 114792 |
| rs145653881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033254 | ACCCACCATATGCCT[A/G]TATAAGTGAGATCAT | 114792 |
| rs145677060 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028567 | TCATATTTTCTCTGA[A/T]CCATGCAGACTCTAA | 114792 |
| rs145701303 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034023 | TTTGGTATGCATAAG[C/G]TTTTAGTTTGATGCA | 114792 |
| rs145738392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008076 | ATGCAGGTGGTTGTG[A/G]TGGTGGTGACATGAC | 114792 |
| rs145745411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936947 | CACTTTCTCAATGAA[A/G]TCCATTGTGATCACT | 114792 |
| rs145749635 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128035 | TTCCATATACTAAAA[A/T]ATGGATGAACCTTGG | 114792 |
| rs145774590 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050991 | CTGGGCAACAAGAGC[A/T]AAACTCCATCTCAAA | 114792 |
| rs145775051 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993814 | GAGCCCCAATTCCCA[C/T]AGGATGACATGAAGA | 114792 |
| rs145779332 | snp | A/G | 0.00597247 | 0.0543191 | | | GRCh38.p7 | 6:97078457 | CATTGATGAAACAAA[A/G]CATTGTTAAAATAGC | 114792 |
| rs145790820 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977095 | ATGAAAGTACATAAT[A/T]TAGTGATAGCTGATT | 114792 |
| rs145802423 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943633 | AGGACCCAGGTCTCC[A/G]AGGTCTTGTCTTTAC | 114792 |
| rs145805709 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984329 | TTGGAATAAGTGCAG[G/T]GTGGCACTGAGAAGA | 114792 |
| rs145824193 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063335 | AGGCCTAAGGAAAAC[A/G]AGAGTCAAGAATGAC | 114792 |
| rs145830748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981086 | ATCACAGGAACAGCA[C/T]GGAGGTAACTGCCCC | 114792 |
| rs145830881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931623 | TTCATAATTCAGATG[C/T]ATTTTTACTAGTTGG | 114792 |
| rs145845540 | in-del | -/TTTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043452 | CATACCATCTTTTCT[-/TTTA]TTATTCATCTGATGA | 114792 |
| rs145852175 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942126 | CATGTGTTGCTCTAA[C/T]ATTCTCCTGCTTTAC | 114792 |
| rs145853399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134275 | GAATTATCAAAGCCA[C/T]ACACACATGAAGAGC | 114792 |
| rs145905223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934422 | CCATCTGGATCTGGG[A/C]CTCAGCTTTCTTGTC | 114792 |
| rs145925414 | in-del | -/TGAGTGAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950613 | AATGAGTTGAGTGAG[-/TGAGTGAA]TGAGTGAATGAGTGA | 114792 |
| rs145935707 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049097 | GCTATATTCCAAGAC[C/G]CCAGTGGATGCCTGA | 114792 |
| rs145941320 | snp | G/T | 0.000800732 | 0.0199931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130717 | TTTTCTGACATGGAG[G/T]TCTCCTACTAACAGA | 114792 |
| rs145961500 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996345 | TGCCTATGTAATTTT[G/T]AGAATTGAGAAAAGG | 114792 |
| rs145971295 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932600 | TTGAGACAGATTCTC[A/G]CTCTGTCACCCAGGC | 114792 |
| rs145973377 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000918 | ATATTACAAAGTGAA[C/T]GAAGCCAGTCTAAAA | 114792 |
| rs145998879 | in-del | -/T/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022470 | GTGATAACACCTAAT[-/T/TT]TTTTTTTTTTTTTTT | 114792 |
| rs146043533 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126993 | CACTGTGTTAGAGTA[C/T]GGATGTTAGAGCTTT | 114792 |
| rs146044684 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043533 | TGAACATGGGTAGGC[A/T]GATGTCTCTATAGCA | 114792 |
| rs146057544 | in-del | -/AAC | 0.0402882 | 0.136092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934447 | TTGTCATTGACACTT[-/AAC]AACAACAACAACAAA | 114792 |
| rs146064144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065759 | TGTAATTTTAAATGT[A/G]TACTTTTATCATTGA | 114792 |
| rs146077052 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019755 | AGCATAAAAGCAGAC[A/G]TTCATGAAACAGCAA | 114792 |
| rs146081428 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945575 | TCCTAGAAAGAGAGG[G/T]GTGCTTTAAAAAGGG | 114792 |
| rs146092432 | snp | A/G | 0.0114712 | 0.0748599 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896884 | CAATATTAAAATCAA[A/G]GAAAATTTCCTGTAA | 114792 |
| rs146093196 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951473 | AGAGGGCTGGGCCAT[C/G]TGGGGCATGTTGGAC | 114792 |
| rs146101217 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105857 | TCACTCATCTGATGA[A/G]AGCCTGCTTTTTAAG | 114792 |
| rs146160970 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063116 | TGTGGTTTTAAAGAA[C/T]CAGTCTGGTTGATAT | 114792 |
| rs146204633 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967932 | GCATGGCATTCATTT[C/G]AATAGTCTCACTGGA | 114792 |
| rs146228988 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110446 | CAGAAAACTAAAAAG[A/T]CAAGCCCAAAATGCA | 114792 |
| rs146268613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132054 | GGAGGGGAAACCTTT[C/T]ATCATTTTGGCGTGT | 114792 |
| rs146286259 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997069 | TGAGGGTCAGGGAGC[A/G]TGGGAGCAAAGGGAT | 114792 |
| rs146296816 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025637 | TTGAATTGAAGGGCC[G/T]ACCAGTTTCCCAGTT | 114792 |
| rs146304108 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107225 | GTGAATCCAGGAGGC[A/G]GAGCTTGCAGTGAGC | 114792 |
| rs146322316 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902844 | TTTATTAAATAGGGA[A/T]TCCTTTCCCCCATTG | 114792 |
| rs146333709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907662 | TTGTTTGCTGCTCAT[C/T]AGAAGAGTGACTCTG | 114792 |
| rs146336152 | snp | G/T | 0.452473 | 0.146644 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985405 | CTGTATTTCCTGAAT[G/T]TGAATGTTGGCCTGC | 114792 |
| rs146354306 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083126 | GCTGGGTGCCGTGGC[C/T]CATGCCTGTAATCCT | 114792 |
| rs146384876 | snp | C/T | 0.142947 | 0.22592 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019848 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAATCT | 114792 |
| rs146406832 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103025 | GTATATTTACCTCTA[C/T]GAGGTAAATAAATAT | 114792 |
| rs146407309 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020163 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT | 114792 |
| rs146415497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922266 | CTGGGAGTACAAAGA[A/G]CAATCAATTGGGACT | 114792 |
| rs146418239 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992362 | GTGGGCAGTTGTCCT[G/T]TCTCACTCTTCTCAC | 114792 |
| rs146452029 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055811 | TAAAAAAAAAAAAAA[A/C]AAAAAAAAAAACCCC | 114792 |
| rs146465511 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098143 | TATAGGCTAAAAACG[A/G]TACAGACATCTAATA | 114792 |
| rs146503529 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053083 | CACACACACACACAC[-/AC]GCACACACATTCTCT | 114792 |
| rs146504105 | snp | C/T | 0.0271762 | 0.113356 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040426 | CATTTGGAGAATTGG[C/T]TGGGGGCAAATTCAC | 114792 |
| rs146522546 | in-del | -/CT | 0.0182019 | 0.0936463 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898115 | GAGTCACCCGGGAAG[-/CT]CTCTGTAAAGTTCTG | 114792 |
| rs146529266 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915775 | TATGAAAAAGGTCAG[A/G]ATATGCCACCCCAAA | 114792 |
| rs146540923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941778 | TTTGTCCTTTACTGA[C/T]CTCTTCCATCTAAGC | 114792 |
| rs146601200 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969945 | TCATTCTCTTCTACA[A/C]TTCTGATTCTCTTTC | 114792 |
| rs146607406 | snp | A/C/T | 0.0483141 | 0.147822 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103403 | TATTTTTGGTAGAGA[A/C/T]GGGGTTTCACCATGT | 114792 |
| rs146614103 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056255 | GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 114792 |
| rs146624824 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059835 | TATTTATGCTGTTGT[A/G]TCCAGTTCATTTGAT | 114792 |
| rs146625441 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985870 | AGCCTTCTTGTCTCA[A/G]CTCGTCAAAGTCATT | 114792 |
| rs146659038 | snp | C/T | 8.23744e-05 | 0.0064172 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114052 | TGGTGGGAAAAAGCG[C/T]GAGGTCTGCAAGGTC | 114792 |
| rs146660369 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963538 | CAATGGCTTTTAGGT[A/C]AAAATGATCCCTGTG | 114792 |
| rs146661684 | in-del | -/CCG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057549 | CTCAGATCTTTTACA[-/CCG]CCCCCCTCCCGCCCC | 114792 |
| rs146714646 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121689 | CAAAACTCTTCTCAC[A/G]GAGAGAACCCCCTTT | 114792 |
| rs146731135 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989560 | GTGAGCCTTGGAGAA[G/T]CTGACAACTGTGCGT | 114792 |
| rs146732913 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127044 | GGACAAGAATTTTCC[A/G]TATAACTATGTCCCT | 114792 |
| rs146742445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992962 | TTCCTTCAGTCTCAT[A/G]AGCTGCTTGTAAGAT | 114792 |
| rs146753526 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077968 | TAGCTTAGTGACAAG[C/T]TTATGTGTATGTGAT | 114792 |
| rs146769395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958486 | GGGGAGAGAACAATT[C/G]AGTGTTGATGAGTAT | 114792 |
| rs146784140 | in-del | -/G | 0.404907 | 0.196224 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985027 | ATTGTTCCTTTCCAT[-/G]TTTAGTGCTTCCTTC | 114792 |
| rs146853382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009543 | GTTGTGTATGGACTG[C/G]AAAAATGCATGCGAG | 114792 |
| rs146854070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094594 | ACCTCCTCCTTGTTA[C/T]GTGCGGTGGCATGTT | 114792 |
| rs146863622 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931417 | CAGCCTACCACATAG[-/G]GAAGTTAGCCTGAGC | 114792 |
| rs146873293 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097480 | GTGCAGTCTTGGATA[A/T]TGCACGGATATAGTT | 114792 |
| rs146904624 | in-del | -/ACTG | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932193 | CCTTGAGCTGATAGA[-/ACTG]ACTGGGTTATTTTTT | 114792 |
| rs146906589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994678 | TGCGTGCAAAGTACT[A/G]TGAGTTCCTGTGATC | 114792 |
| rs146913040 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079038 | TAAGCTAGGCTGTGG[G/T]TTATGTGTGGTAAAT | 114792 |
| rs146913100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134049 | ATAAAACACATTGCT[A/G]TATAACTTATGGGTT | 114792 |
| rs146928831 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105283 | GAAAGGAAAAGATTC[A/G]TCTATGCATCATCAT | 114792 |
| rs146930249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982123 | TAGTTCTCTGCCTCA[A/G]TGATCTATCTAATAG | 114792 |
| rs146930647 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023185 | AACTATATTCATATA[C/T]TACTAAATACATATA | 114792 |
| rs146939171 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899700 | GGCTGTCACCCTTTG[A/G]GAATCATGGAAATAA | 114792 |
| rs146962110 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904206 | AATTTTCCAGGCATG[A/C]TGGTGCACATCGATA | 114792 |
| rs147008184 | in-del | -/ACTAGGT | 0.384593 | 0.210677 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962714 | TGTGTCAGCCTTTGC[-/ACTAGGT]ACTAGGTACACTACA | 114792 |
| rs147013231 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018515 | GGAGAATAGGAGAAT[C/T]GCCTGAACCAGGGAG | 114792 |
| rs147018080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099297 | TGCCTGCCTGTGCTG[A/G]CCATGCTTCTGCTAC | 114792 |
| rs147029922 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046903 | AATTCAGGGTTAACA[A/T]CGAGTGTATCTGCCT | 114792 |
| rs147033754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128158 | ATTCATCAGCTGAAT[A/G]TAATGGGATATGACA | 114792 |
| rs147052538 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994157 | GAAACTCATGGAGAA[C/T]TGTCTCCCAACAGTC | 114792 |
| rs147066340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931049 | TCTTGACAACTAGAA[A/G]TTTCCCTTCATGCTG | 114792 |
| rs147122931 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058834 | GGAGGCTGGTTGCCA[-/CT]CTAAGTGGCCTAATC | 114792 |
| rs147139297 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939753 | TCTTTATCAGAAATG[C/T]CGAGAAGCCATTGAG | 114792 |
| rs147162226 | snp | C/T | 0.0145218 | 0.0839645 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113908 | GTCCCACCCCCTTGT[C/T]CAAGCAAGTGAGACT | 114792 |
| rs147187286 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979541 | TTTTGGTTATTGTAG[C/T]CTTGTAGTATAGTTT | 114792 |
| rs147189018 | in-del | -/GAC | 0.142609 | 0.225759 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023217 | TTTAGAAATTGTAAA[-/GAC]AAAAAAGCCACAATT | 114792 |
| rs147206527 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057659 | CTTTAGCAGATGTAT[C/T]TGTTGCAAATATTTT | 114792 |
| rs147221226 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935977 | TCTGTGATAGGACAC[A/G]GGTTTTATTACTGTA | 114792 |
| rs147263878 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013960 | AGTGGTCTCTGAAGT[A/G]GGGGTTTGTGCACCC | 114792 |
| rs147265556 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141025 | TAAACTAAATTTTAA[A/G]AATGCCTTACCAAGG | 114792 |
| rs147313754 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075314 | TGAATATATCATTAC[A/G]TACAGTTGTCCATAC | 114792 |
| rs147317610 | in-del | -/GT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014970 | GAATCATGGCGGTGG[-/GT]TTTCCCCCATGGTGT | 114792 |
| rs147317752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952569 | AGAATCATAATAGCT[A/G]CTCCCTAAAACTGAC | 114792 |
| rs147318250 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990422 | TTAAGTATAATGGTA[A/G]GTTCTTGCTCAACCA | 114792 |
| rs147327600 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956489 | ACTGTAGCTTGGAGG[A/T]CTCCATATCTTTGAG | 114792 |
| rs147391494 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076134 | TACATACTTGCTTAT[A/G]GTCCAGTATAATGTC | 114792 |
| rs147392911 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983194 | TGTTTATTGATTTGC[A/G]TATGTTGAACTAGCC | 114792 |
| rs147401000 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007816 | GGCAGTGGGGCCCTA[G/T]CTTTGTTCTCTGGCC | 114792 |
| rs147422790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095792 | GAGAAAGTGTGTGTG[A/G]GAGTGAGGATGGATT | 114792 |
| rs147423963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012644 | TGCAGTGAATTTTTC[A/G]TAATTTTTGTGAATT | 114792 |
| rs147452673 | snp | C/T | 1.64844e-05 | 0.00287087 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085260 | CCGCCCAGAAGAAGT[C/T]CTAACGCTTCCCTAT | 114792 |
| rs147455218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919718 | AATATAAATATTATT[C/T]ATGCTCATCATAAAA | 114792 |
| rs147462598 | in-del | -/T | 0.404559 | 0.196498 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045482 | AGTAATTTTTTTTTT[-/T]GTAAAACTACCCAAG | 114792 |
| rs147495988 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096208 | AAGCCACCTTGGATT[C/T]TGAGCCAACAGCCGT | 114792 |
| rs147505160 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956992 | CAATAGAAGAAAATG[C/T]AGAATGTCTTATACT | 114792 |
| rs147506792 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030344 | CATGACTCAAGAAAA[C/T]GTCACATACTGTGAT | 114792 |
| rs147523507 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036745 | ACAAGTGACATCACA[C/T]CCAGGTGTGGGCTCA | 114792 |
| rs147537703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913180 | TTTGACAGTACTGTC[C/T]AGTTTAGGTACATCA | 114792 |
| rs147541250 | snp | A/G/T | 6.59489e-05 | 0.00574196 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132735 | GACAAATGAGCCTCT[A/G/T]GCTTGTATCCAGGTG | 114792 |
| rs147552047 | snp | A/G | 0.00181873 | 0.0301008 | intron-variant, missense | KLHL32 | GRCh38.p7 | 6:97105512 | TTACCTCAATGGGAT[A/G]ACAAGACTGGTAAGG | 114792 |
| rs147568320 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109804 | TTTCCGGTAGTATCT[A/G]TGTGGATGCAGAACT | 114792 |
| rs147596136 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067771 | CATTCAGGTGCATTA[G/T]TTCTCCCACAAAAGT | 114792 |
| rs147600803 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986436 | CTGCAAAGGATTCTG[C/T]TGCCTTTTGTTTGGC | 114792 |
| rs147609407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930036 | CATGCCAGATAAGCC[A/G]GTACCAGTTACTTAG | 114792 |
| rs147672465 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133537 | TATCTTTAATAGTTG[C/T]AGAACTGTTCAACCT | 114792 |
| rs147673064 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050336 | ACACCCCAACAGGAT[A/G]TGAAAAGGTTTATTC | 114792 |
| rs147681233 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931156 | AATTCTCTTTCAAGT[C/T]AGATAGGATTAAAAT | 114792 |
| rs147682826 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055839 | CCCTTCTTATTTCTA[C/T]ATTCCTCTTGAGCTA | 114792 |
| rs147704076 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933364 | TGCCATCCATTCTTT[A/G]TTCATGTGGAAACTT | 114792 |
| rs147706092 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002537 | ATAGGTAAATTGTGC[A/G]TCATAGGAGTTTGGT | 114792 |
| rs147715110 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947779 | TAGTATTATATTAAT[C/G]ATATTTTATAGAATG | 114792 |
| rs147777616 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068796 | GTTATGAATTAAATA[C/T]ATCGTATTAAACCAG | 114792 |
| rs147785045 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949141 | GTCTATTTACTGTTT[A/G]TTCTTCTTAGAATGT | 114792 |
| rs147787638 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072359 | TTCCAAAATTCTGTT[A/T]GATAGATTTTGAAAA | 114792 |
| rs147787784 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022781 | AGCCCTGATCACCTA[A/C]TTTTTAAAGAAGACT | 114792 |
| rs147808027 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953596 | GATTGTACCACTGTA[C/G]TCCAGCCTGGGTGAC | 114792 |
| rs147809170 | snp | A/G | 0.0138799 | 0.0821421 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898298 | ACCAAAGAGTTAGCC[A/G]ATAAAAATGGAACTT | 114792 |
| rs147883289 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088148 | GAGGTAACATAGAGA[A/G]TTGTTCACATACATA | 114792 |
| rs147891467 | snp | C/T | 6.58979e-05 | 0.00573974 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897743 | ATCTTGCTGATTTCC[C/T]GTTCCGCTCGGTTCT | 114792 |
| rs147900113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046572 | TGCCACAGAGTAGAA[G/T]TTGATACCTCTACAG | 114792 |
| rs147910319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049597 | GGGGGGCGGGGGGGA[A/C]CTACTTTATTTTGAA | 114792 |
| rs147910554 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126345 | CTATGCTGTTTTATG[-/T]TTTTTTTTTTTAGAG | 114792 |
| rs147914431 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974303 | CTATCCTAAAGCTTT[A/G]CTTGGCTGATACAAT | 114792 |
| rs147914647 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923574 | AGCAAACGAATAAAC[A/C]CCCAAATCCTGTGGA | 114792 |
| rs147948406 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908594 | AAAAAGACCAAAGCT[G/T]CTTCCTCTATCTCAC | 114792 |
| rs147971697 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057098 | ACTATTTTTAGAAAT[G/T]AATACCCCAAAAATT | 114792 |
| rs147982187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006231 | ATAGTTAGGTCTTTT[C/T]ATTGAGTGAGTCCTT | 114792 |
| rs147985623 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935548 | AACCGCGTCTATCAT[C/G]AATTGATTTTGAACT | 114792 |
| rs148025366 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062169 | CATGTAACACATGCT[A/G]TGGAATATTCATCTT | 114792 |
| rs148062658 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976137 | AACAGAAATTCCATG[C/T]TCACAAGGCAGTCCT | 114792 |
| rs148073516 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949445 | TTCTAATGTTGCCAC[C/T]ATCTACCCCGACCAG | 114792 |
| rs148102038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959502 | CCTGTGTCCTCACGC[A/G]GTCTTTCATTTGTAT | 114792 |
| rs148111328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034468 | CCAGCATGTTCTTTT[C/T]GTTTAAGATTTCTTT | 114792 |
| rs148125533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911687 | ACTGCAAAGCACAAC[A/G]TAAAGTTCAAACTGC | 114792 |
| rs148128502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134746 | GGAAATAAAGAAAAT[A/G]CTGTACGTATCAAGT | 114792 |
| rs148144858 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083935 | GGACAAAAAGCAATG[A/G]TTTTGCTTAAGACTC | 114792 |
| rs148146864 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000427 | TTGAGGAAGCATGTA[A/G]TAAGTTCATTTGTGT | 114792 |
| rs148156204 | snp | A/G | 0.000416351 | 0.0144223 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967100 | TATGCCCTGTAGGAT[A/G]TGTCCTCACATGCCG | 114792 |
| rs148195183 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053886 | TATACTACACATACA[C/T]TACAAAATACATAGA | 114792 |
| rs148200062 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978227 | GGGTTTGGTGTACAG[A/G]TTATTTCATCACCCA | 114792 |
| rs148211817 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983153 | CATGTGGTTTTTGTC[A/G]TTGGTTCTGTTTATA | 114792 |
| rs148236864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019265 | TTTGCAATTTGCGTT[C/T]CTTGGGAAGTAGACT | 114792 |
| rs148280312 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985095 | CTCTCAGTATTTGCT[C/T]GTCTGTAACAGATTT | 114792 |
| rs148283811 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905363 | GGTAAACCCAACTCA[A/G]TAACTCCAGAGCTAG | 114792 |
| rs148303128 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123161 | CAGACTTGACCCAGT[C/T]TGACCATGTACAATG | 114792 |
| rs148322057 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990097 | TGTCTGTCATTTCAG[C/T]CATTTCAGCCTGGTT | 114792 |
| rs148323902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107022 | TTTGGGCTGAGCGCG[A/G]TGGCTCACACCTGTA | 114792 |
| rs148347188 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938052 | TTTCTGATTCCTAAG[C/G]CTCTTTGTCAAGTAA | 114792 |
| rs148353017 | in-del | -/AGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083972 | CCCATCTGCCCCAAA[-/AGG]AGGAGTGTGTGCTAT | 114792 |
| rs148363033 | in-del | -/C | 0.0260105 | 0.111035 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989712 | CAAGTTGCTTTTTCT[-/C]CCCCCCCTCTCTTCC | 114792 |
| rs148366098 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926650 | ATAAAGGAGTGGAGC[A/C]GGCCTAGACAAGACA | 114792 |
| rs148387726 | in-del | -/CACA | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924802 | ACACACGCACGCAGG[-/CACA]CACACACACACACAC | 114792 |
| rs148411330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125574 | AAGTACTGAAGAACA[G/T]TTCAGAGGAGCTTGA | 114792 |
| rs148424263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076238 | CTGACACTCATAGAA[A/G]AACAATGTCCATATT | 114792 |
| rs148428629 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991437 | TTTGTTCCTTCCCCA[A/G]TGCAGTAAGGGTGGT | 114792 |
| rs148432040 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109720 | AGAGAAAAATAATTA[A/T]ATGGGCAGCACTATG | 114792 |
| rs148460758 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940451 | TTCAAGGAGAGAGCA[C/T]TTACTGATGCAGAAT | 114792 |
| rs148465410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049458 | GAGATTGCATCATGC[A/C]ACTCAGAATGGTGCA | 114792 |
| rs148475474 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997213 | GAAGATGTCTGTCCT[C/T]CTTGAGGCTGGAGCC | 114792 |
| rs148479944 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928883 | GGTTGCATATACTTT[C/T]GATGAAGTCTTATAT | 114792 |
| rs148499252 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025712 | CACAGAAGAATGGTG[A/G]TGAAGGCATGGGTTC | 114792 |
| rs148501231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059716 | GTAGAAATTTCTCAT[A/T]GCTAGATAGATCTTG | 114792 |
| rs148511236 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008095 | TGGTGACATGACAGG[G/T]TCAGGGCACTGTGGT | 114792 |
| rs148535151 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088212 | AATATATTGTTTTTT[-/T]AAAATTTAGTTCAAT | 114792 |
| rs148559374 | in-del | -/GA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967500 | ATAGGGATAGAGAAT[-/GA]GAGAGAGAGAGAGAG | 114792 |
| rs148580208 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071364 | CCTCTCTTTCTCGGG[A/G]CTCTCTCCTATTCTC | 114792 |
| rs148594674 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951633 | TGAGCAATATGCATA[C/T]CAAAACTGGTATGTA | 114792 |
| rs148621107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080474 | AAGGCATGAGACACA[A/T]TCTTTGCTTCCGAGA | 114792 |
| rs148628106 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932680 | CAAGCAATCCTACCA[C/T]CTCAGTCTCCCATGT | 114792 |
| rs148656366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138934 | TCCAAAAACATACTA[A/G]CATAGTGTAGCATTT | 114792 |
| rs148666743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001997 | AGATAGATAGATAAC[G/T]CTACTGTAAAGAACT | 114792 |
| rs148667964 | snp | C/T | 0.000379993 | 0.0137787 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896787 | TCAACATACACATCT[C/T]TTAGAAACGACAGCA | 114792 |
| rs148672952 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086794 | TCTCTTATAAACACA[A/T]ATCAACAGAATTTAC | 114792 |
| rs148689391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968745 | GCTCTGCTGTATCAT[C/T]TCCTTGTCCTGAAAA | 114792 |
| rs148700484 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059688 | CAGTGGTTTTGAAAC[-/TA]AAACTAGATTGGTAG | 114792 |
| rs148709818 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096799 | GAACTGTAAGGATTT[G/T]GGGGCAAAGGAACTA | 114792 |
| rs148728203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056038 | ATCTAATTAAATACT[A/G]TCATATGTGACCTCA | 114792 |
| rs148752247 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983800 | TCTTGCTAGCGGTCT[A/G]TCAATTTTGTTGATC | 114792 |
| rs148761920 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103736 | CATGCAAACATTCAC[A/G]CAGACATTTCTGCTG | 114792 |
| rs148795416 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111861 | TTCCCCTGAAGTCTG[A/G]CCATCCCCTGTTGGA | 114792 |
| rs148797180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030090 | TATTTCACCTGTAAG[A/T]TTATTTGTATTCTTG | 114792 |
| rs148804044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908117 | AACAAGAAAACCCCC[A/G]AAAGGATCACAGGGC | 114792 |
| rs148806558 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985816 | CTTTGCCATGGGTAC[A/G]AACTTCCTCCTTTAG | 114792 |
| rs148820460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099004 | TTATCTTATAGGTTC[A/G]CTATGTTTTTAAAGT | 114792 |
| rs148866823 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918408 | TGGCTTGGGAAACAT[C/T]AGTTAAATTTGAATG | 114792 |
| rs148869851 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989951 | CAGATCAGTTTGTTT[C/G]TTTCTTATAATGGCC | 114792 |
| rs148904902 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115559 | ATCTTGTTTTCTCTA[C/T]ACCCACAGACCCATC | 114792 |
| rs148929193 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936993 | ACCTGCCCACCACCC[C/T]AACCCCTTCACTCTC | 114792 |
| rs148968747 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063462 | CACACAAGTGGACTG[C/T]TGGGGAGAGCAAAAG | 114792 |
| rs148981944 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942724 | AGGGTCATATTTGAT[C/T]CTCAAGGAAGAAGAG | 114792 |
| rs149003211 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000333 | TAACTATGCATGCTG[A/G]TGAGCTACAGGATGT | 114792 |
| rs149010456 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958743 | AGGCAATGTTTCCCC[A/T]CCCATTGGAAAGAAT | 114792 |
| rs149020345 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027174 | CTCAAAAAAAAAAAA[A/G]AAAGAAAAAGAAAAG | 114792 |
| rs149024784 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954050 | TTCCTTCACTATCAC[A/C]TGAGAATTCCTATCA | 114792 |
| rs149034421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904400 | TGGTCAAAAAATTTC[A/G]TGGATGATGACCACA | 114792 |
| rs149044610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094869 | TGTGTGTTCTTGTTG[A/G]TGAGGAATGCCCACT | 114792 |
| rs149078142 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959110 | TAGAGAAAGATGAGC[A/G]CTGATTGGAAAATTG | 114792 |
| rs149115354 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073352 | ATAATTAAATGAACC[A/G]TCACTTTCTTTCTGC | 114792 |
| rs149140796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980590 | GTGGATTTTTACATT[C/T]ATGTTCATCAAGGAT | 114792 |
| rs149163682 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933631 | ATGGAAGCATATTGA[C/T]AGTTTCAGGAGAGAG | 114792 |
| rs149184154 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022067 | TTGCAGTATCCTCCT[A/T]GTCTGTTTTCCTTCT | 114792 |
| rs149192863 | snp | C/G | 0.030665 | 0.119967 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897902 | CAAGTGAGGGGAAGC[C/G]CCGCCGCGGGCGCTT | 114792 |
| rs149204425 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089183 | CCTCCTGATTTTAAA[A/C]CATAAGTACAGCTCT | 114792 |
| rs149212791 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971124 | TTTTAATATGTAAGT[A/G]TGTAACACCTTATTG | 114792 |
| rs149222214 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047278 | CTAATGAGAAATATG[C/T]CCTTCTTCTGGGCAC | 114792 |
| rs149251486 | in-del | -/AGCA | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010242 | AGTGATAGAAGCAAT[-/AGCA]GGATCAGCAGAATGG | 114792 |
| rs149251883 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056888 | TATTTTAAAAAGTAA[A/G]TAAAGTTTATTTCGC | 114792 |
| rs149266084 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935274 | CCTGATGTTGAGTTA[C/G]GTACAAACCTGCTCA | 114792 |
| rs149276644 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125432 | CAGATAAGGTTAAAC[A/G]GAGAAAGAAGACTTT | 114792 |
| rs149277006 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041867 | TCTTAAAGAACTATC[A/G]TAAGGGAAAGAGTTT | 114792 |
| rs149293490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106102 | TAAAAGAATCAGGAA[C/T]TTTAGATATCAAAAC | 114792 |
| rs149327445 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946516 | AATTACTTGTTGATT[-/C]TTAAGTCAAGAATCT | 114792 |
| rs149347855 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070803 | GCTAGAGTTCAGAAT[A/C]AATAATCAAAACAAA | 114792 |
| rs149362833 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951568 | TTTGCCATCACTACC[A/G]TCATCTTACCATCAT | 114792 |
| rs149363755 | in-del | -/CAGCTGC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911853 | TTTTTTTTTTTTTGG[-/CAGCTGC]CAGCTGCCACTCCTC | 114792 |
| rs149392637 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990450 | CCACGTGGCTCCTCT[C/G]TATTTCCTCTCGATT | 114792 |
| rs149424496 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931476 | CTAAGCTTTGTTTTC[A/G]TCATACAATGGATTA | 114792 |
| rs149436805 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118398 | CCGAGGCGGGCGGAT[C/T]GCCTGAGATTAGGAG | 114792 |
| rs149451109 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983140 | CTATTGAGATAATCA[G/T]GTGGTTTTTGTCATT | 114792 |
| rs149469676 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011006 | TGCTATACCTAACAG[C/T]CTGCTCAGAAGAAGG | 114792 |
| rs149479460 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977667 | TGAATATTTCTAATA[A/G]TACTGTTGGTTTTGT | 114792 |
| rs149488770 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996231 | TGTCTTGACTGTCTA[A/G]CATAACTTCGTATAT | 114792 |
| rs149490214 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080344 | GGCATATTGGAAAGA[C/T]ATGGGCTATTCTGTT | 114792 |
| rs149500230 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065169 | GTAATTAATTACCAT[A/G]TGAACTTCCCAGGCA | 114792 |
| rs149518717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055290 | CTTCATCATCTTACC[A/G]TCAAATTCTCAACCC | 114792 |
| rs149521523 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944769 | TTTCCAAATCTGTGA[A/C]GTGACAGTAAACTGT | 114792 |
| rs149522991 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018986 | CATTCTCAGCACACA[C/T]GAAACAATTACAAAA | 114792 |
| rs149525812 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138644 | CCAGAATCGACTGAA[G/T]TTTGAATTTGCTACT | 114792 |
| rs149529953 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896365 | ACTTACTAAAGGAGT[C/T]TCTGAGATTAGAACA | 114792 |
| rs149552097 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028898 | GAATGTATTGTGATC[C/T]CACGTTCAGGGGATA | 114792 |
| rs149553667 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925891 | CTATACACAGATAGA[A/G]ATAGATATAAAATGT | 114792 |
| rs149572650 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907974 | AAAGATACATGGACT[C/T]ATAAATAGTGGACAC | 114792 |
| rs149619435 | snp | C/T | 1.64909e-05 | 0.00287144 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085184 | ACCTCTTTAACCTCA[C/T]TTTGTTGGAGAAGGC | 114792 |
| rs149655105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928374 | GAGCTTACTGTAGCT[A/G]AGCGAGTGATGAAAG | 114792 |
| rs149665621 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033098 | AGAGCTTGCCATATG[C/T]CAGGCACTGTTCACT | 114792 |
| rs149678902 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910062 | TACTGGACTGCAGCT[C/T]TATTATGAGGTGTTG | 114792 |
| rs149719002 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040588 | GTCTGTACTCAGACA[C/T]GTTCCCAGGTGATCC | 114792 |
| rs149736295 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034838 | ACAGATTTTTGTATG[-/T]TAATTTTGCACCAAA | 114792 |
| rs149750124 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973438 | TACATTTATTTAACA[C/T]TTAAGGTGATATAAA | 114792 |
| rs149751798 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049348 | CTGATAACCCAGAGG[A/G]CTACTAGGTTACTAA | 114792 |
| rs149765886 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102988 | TCCTCTCCCTCCTCC[A/C]CCACCCTCCACCATC | 114792 |
| rs149781476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059246 | TTAAAGGAATGAGGA[A/G]GACATTGAAGATGGA | 114792 |
| rs149800253 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046421 | TTATACTTTGTTATA[C/T]TTTGTTGAAGGAGGC | 114792 |
| rs149802161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936858 | AGTTGGTAATACCCT[C/T]GGCCTGGAATGCCCT | 114792 |
| rs149807910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127698 | ACCCTTTCAGAGTTC[C/T]GCATAATATAGAAAT | 114792 |
| rs149812424 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920436 | AGTTCCCCAGGTTAG[A/C]GAGTGACACACAGCA | 114792 |
| rs149824676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109527 | ATCACAGTGGTCACC[A/G]TTCCATGGCTAATTT | 114792 |
| rs149828421 | in-del | -/ACACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943037 | GTTCATGCTCCCTCT[-/ACACAC]ACACACACACACACA | 114792 |
| rs149876116 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989019 | AAATGAGAAGTTAAT[C/G]GGTGCAGCACACCAG | 114792 |
| rs149886325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953896 | TATTGTTATCAACAA[C/T]TCAATCCTCAAACTC | 114792 |
| rs149960812 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120225 | TTAAGCCTGGAGGGA[A/G]GGAGATAATTATGGG | 114792 |
| rs149962363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001277 | GAGGGGGAAGGAGCT[A/G]TGTGGAACTCTCTAT | 114792 |
| rs149974469 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983414 | CGAGTTAGGGAGGAT[A/T]CCCTCTTTTTCTATT | 114792 |
| rs149991910 | snp | A/G | 0.127599 | 0.217986 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014220 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 114792 |
| rs149999146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096451 | TTCACCACTCCAAGC[A/G]TATATATTCCATTCA | 114792 |
| rs150015074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980370 | GGGCTTTTAACATGA[A/C]GGGAAGTTGATTTTT | 114792 |
| rs150034938 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067540 | TCAATCTGTGGTAAC[C/G]CATGGCCCCCAGACC | 114792 |
| rs150043108 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947759 | TAAACATGCTGTGAG[A/G]TAAGTAGTATTATAT | 114792 |
| rs150044504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020972 | TTCCTATATGATGAT[A/G]TATTATATAGGGTAG | 114792 |
| rs150055098 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139804 | TTTATTCAAGGTGAT[A/G]CGAATAATAATAGAC | 114792 |
| rs150088625 | snp | A/G/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010246 | GATAGAAGCAATGGA[A/G/T]CAGCAGAATGGGTAT | 114792 |
| rs150101256 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098319 | CTCATCATATATTAG[C/G]CACCTGAGAGCTAGA | 114792 |
| rs150105590 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017655 | GGCAGAGATGGCCAG[C/G]CAATTTAGGTTTCTC | 114792 |
| rs150135723 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069691 | CTGAGGGATTGAAAG[A/G]TGCCTCCATTAAGTA | 114792 |
| rs150137321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964835 | TTAATCCTTAACTCA[C/T]TTTAACTCACCTTTT | 114792 |
| rs150147363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916577 | CTGTTAAAATGGTAC[A/G]TGAGTCCTTGGGTCA | 114792 |
| rs150150163 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950237 | ATTTGTGTTAAAAAA[A/T]AAAACCATTAGCTCT | 114792 |
| rs150159109 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024455 | TTTTGAAACTGAGCA[C/T]ATTTCATTAAAAATG | 114792 |
| rs150172245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901241 | ACAAAACAATTTATT[A/G]TCTTACAGTTTGGAG | 114792 |
| rs150187901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035649 | TATTTTGAATGTGTC[A/G]TCCCACTCTCTTCTG | 114792 |
| rs150190423 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931428 | CATAGGAAGTTAGCC[A/T]GAGCAGTATATTGTA | 114792 |
| rs150196192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117877 | ATAGCAAAATAAGAG[A/G]CTAACTGCAAAGTTA | 114792 |
| rs150244885 | snp | A/G | 0.00013187 | 0.00811895 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114384 | GCAGAAATGAACTGC[A/G]CCAGGTTCTGCCTAC | 114792 |
| rs150297215 | in-del | -/ACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068020 | TACAGACACACACAC[-/ACAC]ACACACACACATACA | 114792 |
| rs150314081 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931214 | AATCTATGTTTTTTT[-/C]TTTTTCTCTGCACCA | 114792 |
| rs150315750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060886 | TGGTCGGTTCTTATC[C/T]CCACCAAAATGAGTG | 114792 |
| rs150325054 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932205 | AGAACTGACTGGGTT[-/A]TTTTTTTTTTTTTTT | 114792 |
| rs150325876 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009682 | ATTCCCTATTTGATG[A/G]AAGTGAAATGTGATC | 114792 |
| rs150329344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939266 | TCAGTAATACTGTTT[C/T]ACTCTGTAAAGAATG | 114792 |
| rs150336585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129694 | TGTGACCAGCCTGGC[C/T]AACATGGTGAAACCC | 114792 |
| rs150339855 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923322 | TTTTTGGTTCAAAGA[C/T]GCTTTCATATTCGAT | 114792 |
| rs150347021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111313 | GATCTGCATTTTACT[C/T]ACCCTTCTGATGTAT | 114792 |
| rs150369337 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064804 | GCCCCCAACAACTGG[A/T]GCTGAATGACAGGTA | 114792 |
| rs150376347 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944079 | TATTCGTTCCCTGTC[A/T]GTTCTTGTCCTCCAG | 114792 |
| rs150396286 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990165 | GAAAAAGACACTCTG[C/G]CTTTTTGACTTGCCA | 114792 |
| rs150398681 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074698 | CTAATTTTCAGCAAT[C/G]TGACTTTGTGTACTA | 114792 |
| rs150484427 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004453 | TTCCTGTCTTCCTAT[G/T]TGGATGCCTTTCATT | 114792 |
| rs150490295 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123757 | CGATAGAGGAAGGCA[C/T]GGAATCTATCTTTGC | 114792 |
| rs150492545 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088236 | GTTCAATTCAGCTCA[A/T]CAATTTGGTTTTATG | 114792 |
| rs150599282 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006902 | GGTGACCAACCCCTT[C/G]TCTCTAGATGCTTTT | 114792 |
| rs150616274 | snp | C/T | 0.159622 | 0.233092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985314 | TTATCATTTTTTCCT[C/T]CATTTCAGCTTTGGT | 114792 |
| rs150623238 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912831 | GATCCAGTTCCTCTG[C/T]ATTGTAATTGCTGCT | 114792 |
| rs150632140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102372 | TAGTCCCTATTGCCA[A/G]TGTGATACAGAAGGG | 114792 |
| rs150632317 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987189 | TGATTTTTTGAAGGG[A/T]TTTTTGAGTCTCTAT | 114792 |
| rs150662735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041689 | TGAGATTTAGTTATT[A/G]TTCTTGTTACTCATT | 114792 |
| rs150666528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967244 | GGTGGCACAAGGACT[A/G]ACTGCTGTGACCTAC | 114792 |
| rs150676017 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920128 | ATAGGCTTCCCTGGG[A/C]TGGGATGATGGGAAG | 114792 |
| rs150680875 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026096 | AGAAATAAATACATT[A/G]TATATATATAAATGT | 114792 |
| rs150689466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108701 | TACATTTATGTGTTT[A/G]TTATTGCAAAGGCAA | 114792 |
| rs150718684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932955 | TAATTATTGTCATTA[C/T]ATTTTGTTAATTGCT | 114792 |
| rs150719274 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119554 | GAAATTGGAAGAAGG[C/T]GGAAACTAGAATACA | 114792 |
| rs150752710 | snp | A/G/T | 1.65012e-05 | 0.00287234 | synonymous-codon, missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064705 | GGAGCTTCTCAATTT[A/G/T]TGCTCCCACTATCTC | 114792 |
| rs150756040 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048639 | ATGCAAACACTGTGC[A/G]TTACATTTTGATGAT | 114792 |
| rs150765629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936260 | ACATTTTGCATGGCC[A/G]TTCATTTCTCTAAAG | 114792 |
| rs150801774 | in-del | -/A | 0.0689305 | 0.172377 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108896 | TACCTGCTTAAATTT[-/A]AAAAAACAGAGTGAA | 114792 |
| rs150809781 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054868 | TGCTTGAACCCGGGA[A/G]GCAGAGGATGCATTG | 114792 |
| rs150862584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013391 | AAAATGGAGAGAATG[A/G]TACCTGTTTTGTTAT | 114792 |
| rs150872296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995334 | ATAACTTTTTAATTT[C/T]ATCCTTTCCCAACTT | 114792 |
| rs150879118 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111961 | TGACATTTAGCTGCT[G/T]CTTCTCCTCTTGATG | 114792 |
| rs150893611 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067328 | CAGGAGCAGTGCTCC[G/T]CTGTGTCAATGAGGA | 114792 |
| rs150897558 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985890 | TCAAAGTCATTCTCC[A/G]TCCAGCTTTGTTCCA | 114792 |
| rs150946068 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030753 | TTTAGCTTACAGTAG[A/T]TGCTCTTTCTCTTTA | 114792 |
| rs150950810 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958055 | GTGGATCCTGCCCAT[A/G]TAGACAGGATGACCA | 114792 |
| rs150955051 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063892 | TTTGTCAACATGGTC[C/G]TGTGCCTTTTTTCCA | 114792 |
| rs150960425 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909386 | TCTGTCTTGGGACCC[A/G]GTTTTTAGATTCAAC | 114792 |
| rs150969889 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943258 | TTTTCCTCAAAATGG[A/T]TTTGGCTTATGGTAA | 114792 |
| rs150984446 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082440 | AACACGGTGAAACCC[C/T]GTTTCCACTAAAAAT | 114792 |
| rs150987095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997601 | AAAAAAAATTAGCTG[A/G]GTGTAGTGGCATGCA | 114792 |
| rs150988830 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115966 | AAATTCTCCCTTGCA[C/G]TTCTTTAAATTCATT | 114792 |
| rs151008291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068965 | GGCGTGCTGCTGGGA[A/T]GTGAGAGGCTGGGAC | 114792 |
| rs151020921 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105079 | CACTTGCATTAGGGA[A/G]ACATCACATTTTTAA | 114792 |
| rs151032702 | snp | C/T | 0.000248729 | 0.0111491 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976084 | GAATCAGCAGAGGAG[C/T]GATGGCATCCTCTGC | 114792 |
| rs151067312 | snp | C/T | 4.94515e-05 | 0.00497225 | synonymous-codon, intron-variant, stop-gained, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113830 | CTACCAGTACATGGA[C/T]GAGCTCCTGCAATAC | 114792 |
| rs151075035 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087493 | TTGTTCATTACGGAA[C/T]GTTCTCACTGTAATA | 114792 |
| rs151119489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903069 | TAAATCAAAAAATTT[A/C]TTTAAAGGACTGAAG | 114792 |
| rs151129610 | snp | A/G | 0.0456336 | 0.143994 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008478 | AGGCTAATGTCTCCT[A/G]GAGGAGCGTAGGTGT | 114792 |
| rs151156839 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988974 | TTGGGGGAGGGAGGA[A/G]GGATAGCATTAGGAG | 114792 |
| rs151161960 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915201 | TAATTTAATCTCAAT[G/T]GTACCTACAGCTGTT | 114792 |
| rs151164153 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103897 | AATTAGAGAATTCTA[C/T]TTTAAAATATTTTTG | 114792 |
| rs151177861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060692 | CTTGGATTGGTGACC[A/G]GAGGACATGTTGGCA | 114792 |
| rs151192075 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969039 | CTGTAGTCGGGGTCA[A/T]TGTCCTTTATTCACT | 114792 |
| rs151200448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045033 | AGAGGCTTATTAAAA[C/T]GTATGATATCATTTA | 114792 |
| rs151215379 | snp | A/C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922794 | GGAGTAAACTGCAAC[A/C/G]TATGTTTGTGTTGAA | 114792 |
| rs151215954 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110759 | TCCTTGACAGCTTTG[C/T]AGGCGGGAACCGGAG | 114792 |
| rs151218921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027626 | TCTTACCACTGCCAC[C/T]ATTCACAAGCTTAGG | 114792 |
| rs151235500 | in-del | -/T | 0.240478 | 0.249819 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034119 | CCAATGTCAAGGAGC[-/T]TTTCCCCTACATTTT | 114792 |
| rs151243415 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934255 | TTCTATACTTACTGT[G/T]TGAGAATCTGCATTA | 114792 |
| rs151284551 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132555 | GGAGTATACAAATGT[G/T]CCACAAAGGAAAATT | 114792 |
| rs151322172 | in-del | -/CTGAGTA | 0.0283406 | 0.115616 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132497 | TAGTGCTTAATTTTT[-/CTGAGTA]CTGGGAGGCAGTGAT | 114792 |
| rs151333755 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056075 | CGTGCAGCATAGCCA[A/G]CCTCCCTTTTCTTTT | 114792 |
| rs180672009 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973748 | TTTTTTTTTAGACAG[A/G]GTCTCGCTCTGTTGC | 114792 |
| rs180673509 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996315 | TCTTTTTCCGTTAGA[A/G]GCTGGGCGTGCTCCT | 114792 |
| rs180681520 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988811 | CCTTTGTAGGGACAT[G/T]GATGAAGATGGAAAC | 114792 |
| rs180689834 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016546 | CTAGGAAGTAACTAA[C/T]TTGCTTTTGATTTTA | 114792 |
| rs180696275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905946 | GTCCTTGCTCATAGA[C/G]TTTTTGGATTAGTTT | 114792 |
| rs180697684 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956747 | CATTTAATTCTTATA[A/G]TGTTCGATTGTTGTA | 114792 |
| rs180698835 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944434 | GGAATGCTGTTTGTG[A/G]GGAACAAATTAGTTT | 114792 |
| rs180701565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982828 | ATGTCATCTGCAAAC[A/G]GGGACAATTTGACTT | 114792 |
| rs180711709 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926463 | TTAATCCTCACAACA[A/G]CCCTTTGAGGCCAAT | 114792 |
| rs180731076 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916239 | CTATGAGTGGTTGAA[A/G]TATGGCTGCTAGGAT | 114792 |
| rs180825297 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117069 | TACCTTCAGTCATCT[A/G]CCTCTTTCCTCAGGC | 114792 |
| rs180961717 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103546 | CAATATTACCTTGAA[G/T]CAGTCACCTTAATAA | 114792 |
| rs180967772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120548 | CTGTGGATTCACTCA[C/T]GATGAAAGGTTATGA | 114792 |
| rs180971525 | snp | A/T | 0.126219 | 0.217206 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112765 | GAATTTTTTTAATTT[A/T]AAAAAAAAAAAGGAG | 114792 |
| rs180974479 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142317 | ACATCAAAAATTTTA[A/G]TAAGTATAAACTGGT | 114792 |
| rs180979802 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062105 | AAAGACAAAAACAAT[C/T]GCCGTATGGGTTTTT | 114792 |
| rs181001164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085850 | CCATCCTTAGTTCAT[C/T]CTGCATTCATTGCTA | 114792 |
| rs181032986 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042711 | ATTATAGTTACCATT[A/C]TGTGAAGTAGATCAC | 114792 |
| rs181052863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007504 | AGCCATTTCAGCCTG[G/T]TTAAGAACCATTGCT | 114792 |
| rs181085320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027879 | CCAGTAGGAGACTCT[A/G]GAGCTGTTACTGTAT | 114792 |
| rs181149252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121213 | GAGTTAGAATTTGAA[C/G]TCTGTGTCTCTGGTT | 114792 |
| rs181150719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104576 | ACAGTATATGAGCCT[C/T]GGGCCTCATCAGATT | 114792 |
| rs181162443 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094842 | AGAGGCTGAGGACAC[A/C]TATCTTCTTTGTGTG | 114792 |
| rs181163792 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111105 | CCTTCCAGCAACACT[A/G]AGGAGTGGCCTTGGC | 114792 |
| rs181171267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129333 | TTTTTCTTGGCAAAA[A/G]GGAATCTGGGTTCTT | 114792 |
| rs181174984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043758 | TAGTAGGGGTGAGGC[A/G]ATATCTCACCATAGT | 114792 |
| rs181182375 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035480 | ATGTTTTTGTTTTCA[A/G]TTTGAAGAACCCCCT | 114792 |
| rs181184047 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062339 | CCTCCTTAGGCCATG[C/T]CTCTTCTGCAAGACT | 114792 |
| rs181185156 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086628 | TCAATATTCCACACT[A/G]TCTTGATAAAGAAAA | 114792 |
| rs181189373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075472 | TTTTTTCTTCTATAA[A/C]AATTAGACTTTATCC | 114792 |
| rs181191422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052920 | ATAACCCTCTTAATG[C/T]CTGCTGGGAAATTTC | 114792 |
| rs181194491 | snp | A/G/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007900 | TGTCCACAACACCCC[A/G/T]ATGAGGGCTGCCCAC | 114792 |
| rs181201160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059254 | ATGAGGAGGACATTG[A/C]AGATGGAGAACAAGG | 114792 |
| rs181204867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028072 | CTCATCACTTCAAGT[A/T]TTCAAGTATGCAAGG | 114792 |
| rs181206427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017083 | TGAAAATGGACTAAA[C/T]ACAGGTTGGAAATGT | 114792 |
| rs181215579 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081740 | TTACCTCAGTTATAG[A/T]TTTCCATGTAATTGT | 114792 |
| rs181220502 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100008 | AAATTAGCCAGGCGC[A/G]GTGGTGCACACCTGT | 114792 |
| rs181232733 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996768 | GTTCTCAGGCAACTA[C/T]TCTAAATGTTTTATG | 114792 |
| rs181238606 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956991 | TCAATAGAAGAAAAT[A/G]CAGAATGTCTTATAC | 114792 |
| rs181244652 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983700 | TTCTCTGATGGTAGT[G/T]TGTATTTCTGTGGGA | 114792 |
| rs181245783 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916386 | CTTTCTCAGGACATA[C/T]TTAGTTTGCTTTAAC | 114792 |
| rs181290933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124608 | GTGTCATAAAACAGA[C/T]AGTTTACTACAGTAG | 114792 |
| rs181300873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048658 | CATTTTGATGATCAT[C/T]GAAACTGTATTCCCC | 114792 |
| rs181318776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090486 | CAGTTTGAATTAATC[A/G]TTTTCTTCAAAAGGA | 114792 |
| rs181324232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991777 | TCCCTTCCAAGAAAG[C/T]GCAGAGCTGCTACCG | 114792 |
| rs181329222 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032265 | AGGATAAAATTAAGT[A/C]TCTTTTTTCCCTCTA | 114792 |
| rs181336457 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013152 | ATTGTACATTTTCTT[A/G]TGAGAAATAACATTC | 114792 |
| rs181338451 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949769 | CTCTCTTTTTTTCCC[C/T]TCCTAAATTTTAATA | 114792 |
| rs181347275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978554 | TACCACTGATGGTCA[C/T]TTAAGTTGATTCCAT | 114792 |
| rs181349940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930037 | ATGCCAGATAAGCCA[A/G]TACCAGTTACTTAGA | 114792 |
| rs181364777 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937437 | ATAACTAGCGTCAGG[A/C]CATGGGGAAATTGGA | 114792 |
| rs181365551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911525 | AAATCTCCTCCAGTG[C/T]TGTCTCCTCTACCTT | 114792 |
| rs181377909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964844 | AACTCATTTTAACTC[A/G]CCTTTTGAAAAAAAT | 114792 |
| rs181378954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108733 | AATGCAGAGTGTTTC[A/T]ATGGCTTACTTTATG | 114792 |
| rs181393890 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938483 | CTCATCAGCATTCTC[C/T]GTGCTGCTGTTGCTG | 114792 |
| rs181402263 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900272 | GTACAATGCCCAGCT[C/G]AGAATCTGATGTTCA | 114792 |
| rs181402684 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900718 | AAAGGATTACAGTAG[C/T]TAAACCCAGGTGACA | 114792 |
| rs181403911 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922519 | TTAAAAAAAAAAAAT[A/C]TTCTTCAGCTCATCC | 114792 |
| rs181411385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069199 | GAGGAACATAAAGGG[A/C]ACAGGAGGGAGAAAG | 114792 |
| rs181483321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002094 | AGCTGGTTGTATGCT[C/T]CTAGTCCAAGTCTGA | 114792 |
| rs181510640 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919965 | GTTAAGAAAACCAAT[C/T]AACCAACCGAATTTG | 114792 |
| rs181584662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129990 | AGATGTGACTGTTAA[C/T]ATATTAAAGGAGGCT | 114792 |
| rs181605979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950740 | AGAATTAGCATGTTC[A/G]TCACACCAATTAACA | 114792 |
| rs181622257 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986216 | GCAGATGTTGCTGCC[G/T]GATCGTTCCTCTGGA | 114792 |
| rs181698697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091049 | TGCAACATAGTGAGA[A/C]CCCTGTCTCTACGAA | 114792 |
| rs181704667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135550 | TGAACTGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 114792 |
| rs181710906 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109620 | TAGTAACACTGCTTG[C/T]TGGAAAGATAAAGAT | 114792 |
| rs181719477 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125660 | GTGATTAGGCCATCT[A/G]TGTTTGGTGCAAATT | 114792 |
| rs181722674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048954 | TCCCAATCCTTTCTT[C/T]AGCTGGCAGTACCTA | 114792 |
| rs181725294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032627 | GTCCTGCTGTATATA[C/T]GGGATTGGTGGCAAG | 114792 |
| rs181730285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069777 | ACCAGCCTTTCATTA[C/G]TTTTGCCCACTGAAT | 114792 |
| rs181741963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992741 | AAAGAGTGCCTCCTT[C/T]GTAATACCTATATTA | 114792 |
| rs181757887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013887 | TGTCAAAAGGGATAA[A/G]TGCTCATTTTATAAA | 114792 |
| rs181788945 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081381 | ACATAGAGGAGGTGA[C/T]TTAGAGTATGGGCTC | 114792 |
| rs181805582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023335 | TTGACAATCTATAAA[C/T]TATAAGCTGACAATC | 114792 |
| rs181810120 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002592 | TCCTAAGCGTAGTAC[A/G]CTATAGGTGTATTTT | 114792 |
| rs181824761 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986433 | AGTCTGCAAAGGATT[C/T]TGCTGCCTTTTGTTT | 114792 |
| rs181833107 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966302 | TAATTTATTTTTCTA[C/G]TCAGAGTTACTCCAG | 114792 |
| rs181844852 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939362 | CAGTGGTGAGGAAGA[G/T]AGTCAGGAACTTGTC | 114792 |
| rs181869284 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081029 | AGATTTTGTTATTAT[G/T]GAGTTATGGTGAGGC | 114792 |
| rs181886809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115340 | GTTTGTTTGTTTTTA[A/G]TTATCCGTGAATGGT | 114792 |
| rs181906669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084919 | GGGTTTTAAGAGGAG[C/T]AAAATGAGGAAAAAT | 114792 |
| rs181907880 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910894 | AATTAATTGCCAATT[A/T]TATTTTAAATACCAT | 114792 |
| rs181910683 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027514 | AGCCACATGAAATTC[A/G]TCTTAAGGAAAATTG | 114792 |
| rs181912789 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039363 | AGACATAGAGTAGAT[C/T]GGTGGTTACCCTACC | 114792 |
| rs181920510 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007136 | GGATGCTAATGAATT[A/G]TAGATTTGGTCTCTT | 114792 |
| rs181922220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042390 | AGAAGGATGCATGTG[A/G]TCAGGTGTGGCTATC | 114792 |
| rs181922456 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958308 | GGATCTATAGGTGCT[A/G]TTGGATCATATAGGA | 114792 |
| rs181940342 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111675 | ATGGCTTAAATATTA[A/T]CAGCTCAGTGGAGGG | 114792 |
| rs181947814 | snp | A/C | 0.158962 | 0.232835 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987894 | CTGGGAAAACTGGCT[A/C]GCCATATGTAGAAAG | 114792 |
| rs181958127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916604 | GTCAAACTGCTTCAT[C/T]GGTTCTTCCATTCTT | 114792 |
| rs181959771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971703 | CAGGCAGCCTGACGG[A/G]GGTTGCCTAAAGCCG | 114792 |
| rs181965365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136331 | CAATGTTGAAAAAGC[A/T]TACTTTATTTCCTGC | 114792 |
| rs181966009 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896159 | ATCATAGGCCCTGTG[A/G]AAATAAGGACTAGTT | 114792 |
| rs181994515 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099177 | CTTCTTCCCTCATAC[A/G]CCTGCATGACATGAC | 114792 |
| rs182000839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068220 | TCACCTTGCCCAAGC[A/G]TATTATATTGTTTTA | 114792 |
| rs182031547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991167 | CTTCCCCAATGCAAG[C/G]GCAGCAAGGGCAGGA | 114792 |
| rs182037892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031857 | AGCAGTTGAGTGGAG[A/G]GTGCTGTTTCTCAGC | 114792 |
| rs182047540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934709 | ATGGTAGCTCGGTTG[A/T]TTAATAACATACATT | 114792 |
| rs182051436 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922969 | CATTTAAACCTCAAC[A/G]CCATGTGTCAATGAA | 114792 |
| rs182070952 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948456 | GAGACCTACAGAAAA[A/T]TTTTGTGATGTAGGT | 114792 |
| rs182128137 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119917 | GTTGGTTGAGAAAAG[A/G]AAGCAAGAGGGGAGT | 114792 |
| rs182132961 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095269 | AATTTCTCATTCTGC[A/C/T]CACTGCTGGGACTAT | 114792 |
| rs182157866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098110 | AAATCCAGCACCTAA[A/T]CTTGCAGCTATTTGA | 114792 |
| rs182160658 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018205 | AAAGAAACAGAGAAA[A/G]CATGGAATGTAAAAA | 114792 |
| rs182161519 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053339 | GCTACAGCCCATTAG[A/C]TCTGCCTATGAAAAT | 114792 |
| rs182174437 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022126 | CAATACTGCAGCCCC[A/G]GTGAACCCACTGAAA | 114792 |
| rs182185598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058208 | GTTCTCCTTCAACAT[C/T]GTGTTGGCTATTTTG | 114792 |
| rs182193121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983750 | ATCATTTTCTGTTGC[A/G]TCTATTTCATTCTTC | 114792 |
| rs182213710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944039 | AAAGCTAGTTCACCA[C/T]CAGCATTAATTTGAC | 114792 |
| rs182239472 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904634 | ATAGCGTTTTTAATG[A/G]AGCTCGATCACTGAT | 114792 |
| rs182242855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116034 | GGAAGATAGTCACAG[A/G]CTCAGCTTCTCTGAG | 114792 |
| rs182291392 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048165 | AGAGATAAACTCTGC[A/G]CCAAATGATAGTGAC | 114792 |
| rs182312595 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012259 | TTGAGGTGGCAATAC[C/T]ATCCTGGATTATGTA | 114792 |
| rs182330345 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019002 | GAAACAATTACAAAA[A/G]TGATAGTTAAGTAGG | 114792 |
| rs182338779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055667 | ACCAGGTGTGGTGAC[A/G]TGTGCCTGTACTCCC | 114792 |
| rs182342500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036178 | GCTTCAGAATTTGTT[A/T]GCTTCATTTTTGTGG | 114792 |
| rs182344217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984499 | TCTCCCATTATTATT[A/G]TGTGGGAGTCTAAGT | 114792 |
| rs182351825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978357 | CATCCAAGTATTCTC[C/T]GTGTTTAGCTCTCAC | 114792 |
| rs182355897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998171 | GCTTAAAAACTAAAA[C/T]TAAAAATAAATATAC | 114792 |
| rs182356086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908358 | TGTTCAAGAATAAAC[A/G]TATACTTGTAATGAT | 114792 |
| rs182358457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959695 | ATTCAGCTCACATCA[A/G]GGCCTCCTTGGGAGA | 114792 |
| rs182359208 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901260 | TACAGTTTGGAGATC[A/G]GAAGTCCAAAATGAG | 114792 |
| rs182360383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927643 | AAAAGCCAAAAGATT[C/T]GAACAGCGACTTCTC | 114792 |
| rs182362635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929787 | TTTTTAAACGAACTA[C/T]GTAGGAAAAAAAACA | 114792 |
| rs182370788 | snp | A/C | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897338 | ATCGTCCAGTGAAGA[A/C]CCCTAGAGAAAGCTC | 114792 |
| rs182386599 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112902 | CAAAATTAAACAATA[A/C]TTTTTATTATGTATG | 114792 |
| rs182393870 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132927 | ATGATGCCTAAATAA[A/G]TTATTGAGCCCTATT | 114792 |
| rs182397078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088393 | TTTGTGACCTGGCAA[A/G]TCTCTATCTGTTTGA | 114792 |
| rs182398672 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106596 | AAAAATACAAAAAAT[A/T]GCTGGGTGGTAATGG | 114792 |
| rs182404364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076884 | ACATTGTAAAATATT[C/T]AAATATTTTTAGAGG | 114792 |
| rs182410993 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056296 | ATTTTTAGTAGAGTC[A/G]GGGTTTCACCATGTT | 114792 |
| rs182418862 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078150 | ATTTTTATGTAGAGT[A/G]GTTTCTCAGGCTGTT | 114792 |
| rs182422127 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035905 | TTTTGGTAATTATTC[C/T]TTTTCAATAATCTTT | 114792 |
| rs182422434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096450 | TTTCACCACTCCAAG[C/T]GTATATATTCCATTC | 114792 |
| rs182433334 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036938 | TGGGGGGATATAGTG[A/G]TCAAGGCAATTTCTG | 114792 |
| rs182437519 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103415 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 114792 |
| rs182455820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997650 | TGAGAGGCTTAGCAG[A/G]AGGATCGCTTGAGCC | 114792 |
| rs182488094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926143 | TGCACGAATTTCATG[C/G]CTCCATCACAAACAA | 114792 |
| rs182532404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015163 | TGCAACTGTGAGTCA[A/G]TTAAACCTCCTTTCT | 114792 |
| rs182534626 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126459 | AGAAGTATGAGGACA[A/C]ATAAGAGAAACTTAG | 114792 |
| rs182539729 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050728 | ACAATGTGGGCTGGA[C/T]GCAGTGGCTCATGCC | 114792 |
| rs182545601 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033630 | AATGGCTGTACCAAT[G/T]TACATTACAACCAAC | 114792 |
| rs182563459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994180 | CAACAGTCACATGCC[C/T]TAAACTAGAATATTT | 114792 |
| rs182564938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092705 | TAATCTTTCCTTCTA[A/C]TCTATATGCGGCTAA | 114792 |
| rs182571551 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980916 | ACAGGGCTGGGGAGA[A/C]CTCAATAAACTTACA | 114792 |
| rs182579746 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932903 | TTTCTGTGTTTCATG[A/C]TGTTTTTATCAATGT | 114792 |
| rs182589787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913900 | TTATATTACCTGACA[A/G]AGGAGAATTAAGACT | 114792 |
| rs182598530 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989070 | GTAACAAACCTGCAC[A/G]TTGTGCACATGTACC | 114792 |
| rs182608292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917956 | TGTTCCGTACATTGT[A/G]GGATGTTTAGCAGCT | 114792 |
| rs182616715 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975186 | ACATAAGGATAAATG[C/T]TTTAGGTTGGGGTAG | 114792 |
| rs182623012 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926840 | TTATGAGGTATCCTT[A/G]ATTTTAAAAACTGTA | 114792 |
| rs182627834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945210 | ATCCTAGCACATGGC[C/T]GTGCCAGCCCTTTAT | 114792 |
| rs182647677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906373 | GGATGGGTAAAGAGA[C/G]CGGGAGAATGGGATA | 114792 |
| rs182697050 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077660 | CTCAGATTAAGTACT[C/T]AAGAACACTTTTCTC | 114792 |
| rs182715616 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046182 | CTTCTGAAAAAGCCA[A/C/G]GGGACAGCACTAGGC | 114792 |
| rs182733068 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010595 | CTCAATTTTGTGTGT[C/G]TATGAGTGAGGAACC | 114792 |
| rs182735519 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976628 | TTTGAGACAAAGTCT[C/T]GCTCTTTCACCCAGG | 114792 |
| rs182818304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106658 | CTGAGACAGGAGAAT[C/T]GCTTGAGCCTGGGAG | 114792 |
| rs182839817 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071809 | TGACGTCATTCGGGT[G/T]GGGACTATTTTTCCT | 114792 |
| rs182846911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110059 | AATAATTGGAACCCC[A/G]TGTCTTGAAAATTCC | 114792 |
| rs182852038 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998952 | TAATAACTAGAACAA[C/T]GTTAGTTAGAAATTG | 114792 |
| rs182852531 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902429 | GGCATGTTCTTTGCA[A/T]ACTTTTTAATTGGAT | 114792 |
| rs182863600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133994 | ACAATGCAATTAAGT[G/T]AGAACTTAACAAAAA | 114792 |
| rs182908913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960573 | ATGTGATAATAGCAT[A/G]AATAAACCAGTGTTG | 114792 |
| rs182911332 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918275 | TGAGAGAACTTGAAA[A/T]AAAATTTGGGGAATT | 114792 |
| rs182952640 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110262 | TATTTAGTTAAAAAT[A/G]CTACCTTCTATAAAA | 114792 |
| rs182957504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127169 | CAGAATTGGGGTCCT[C/G]TTGGTAATGTCAGCA | 114792 |
| rs182974846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072135 | AGAAAACCAGGAGTC[A/C]TCCTAGAATCTCCCA | 114792 |
| rs182976338 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052142 | AAGTTTGTGTTTAAA[A/G]TCCTTTATATTTCAG | 114792 |
| rs182982853 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028607 | CTCAGTCATTCCTTC[A/G]TGCAAGCCCCAAATT | 114792 |
| rs182991775 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093105 | GCTGCTGTGAGAAGG[A/T]AAAAGATGACTGTAG | 114792 |
| rs182994324 | snp | C/G/T | 0.000716094 | 0.0189088 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064773 | TTCACATTCCTTTCC[C/G/T]CACAGTCATAAGCTG | 114792 |
| rs183001517 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990211 | TTCTTTCTTATCTCT[A/G]TGTGCTGATGTTCCT | 114792 |
| rs183011214 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034439 | ATATTTTGAAATCAG[A/G]AAGTGTGATGCCTCC | 114792 |
| rs183021120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087637 | AACTGGATGGAGGGG[A/G]GCGTGCTATTTGATT | 114792 |
| rs183027039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106020 | TGTTTTGGCATTCCT[C/T]TGGGGTCATAGTGTA | 114792 |
| rs183029038 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946869 | ACAAATGAGAAATGA[C/T]GGTAAAAGAAAAACA | 114792 |
| rs183053051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025182 | GAATCTGTAGAAATG[C/T]CATGATTCTGTTTAT | 114792 |
| rs183061509 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986572 | AAGCCTTGGCAATGG[C/T]GGGCGCCCCTCCCCC | 114792 |
| rs183065902 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123855 | TTGATGACTTTCAAA[G/T]CCAGGAATACTGCTG | 114792 |
| rs183069325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939928 | GTGGGAATAGAGAAG[G/T]AGAGAAATTGCCTAA | 114792 |
| rs183102506 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901754 | TCCGACCTCCAACAG[G/T]CTCCAGTGTTTGTTG | 114792 |
| rs183149438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019484 | GATTAGTCACTGGAT[A/G]TGGGCCACCCCGGTA | 114792 |
| rs183169154 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003682 | ATATACTGTAAGGAA[G/T]GGGTCTAGTTTCAAA | 114792 |
| rs183177424 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931398 | ACAGCAGCAGGAACT[A/G]CTAGCAGCCTACCAC | 114792 |
| rs183178363 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986838 | GTGAGACGATGCCTC[A/G]CCCTGCTTCAGCTCA | 114792 |
| rs183179554 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984577 | GTATTGGGTGCATAT[A/G]TATTTAGGATAGTTA | 114792 |
| rs183187775 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935283 | GAGTTAGGTACAAAC[A/C]TGCTCAATTCCTATT | 114792 |
| rs183189759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967947 | GAATAGTCTCACTGG[A/G]GGTAAATCTGCATCA | 114792 |
| rs183200325 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923730 | ATAGGATTAACATAC[C/T]ATCTTTGCAGTAAGT | 114792 |
| rs183207756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941917 | ATAACTTTTTGAGAA[C/T]CAAATAAATGGTCCA | 114792 |
| rs183231267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125944 | TACATCTCAAAGAGG[A/G]AGAGAAAGAAGTTAT | 114792 |
| rs183243605 | snp | C/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082555 | GAGGCGGAGCTTGCA[C/G/T]TGAGCCAAGATAGCA | 114792 |
| rs183246933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101135 | CTTGAATCAATTCAT[A/G]AACAAATATTCAAAG | 114792 |
| rs183258903 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97041814 | GAACATAGTATTTTA[A/T]ATTTAACTCAGTGCT | 114792 |
| rs183266905 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109823 | GGATGCAGAACTGTA[A/G]GGATATAAGAATGCC | 114792 |
| rs183284151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025990 | AAAAAACTATTTATC[C/T]TTCTTTTAATGATGG | 114792 |
| rs183287349 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987021 | CTTGGCTCCACCCCC[C/T]AGTAGTTTGTATTTC | 114792 |
| rs183289842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005056 | GTTTTAGTGGGAATG[C/G]TATCAGCACTTTTTT | 114792 |
| rs183300245 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968308 | ATCTACTGGGTAGAG[A/G]CCAGGAATCATTTTA | 114792 |
| rs183301019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003232 | ATGGTTTTGATTTCC[A/G]TTTCTCAAATGATTA | 114792 |
| rs183309326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040648 | GAGAACAACTGAAAC[A/G]GAGTGTGTGATACAT | 114792 |
| rs183316737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967711 | ATGTATATTCTATGG[C/T]GAAAACAGACATTAA | 114792 |
| rs183353409 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923226 | GATGGGCTTAAAATT[G/T]TAAGTATTCTCACTT | 114792 |
| rs183374476 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044653 | TTTTCTTTAATGGGA[A/G]ATATTTTTTATTAAT | 114792 |
| rs183383198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096638 | CTTTTTGATATCCAC[A/G]TTGGATTGGTGGGTT | 114792 |
| rs183391474 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063134 | GTCTGGTTGATATTA[A/T]TAAAACAGATAGTGT | 114792 |
| rs183409096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008579 | TCCTGCCACCTCTCC[G/T]GGCAGCTCTCCCTGC | 114792 |
| rs183410584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989459 | AGGGTTTCTTTTGAA[A/C]GGCATGCTGTTAGCT | 114792 |
| rs183411725 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056382 | AGTGCTGGGATTACA[A/G]ACGTGAGCCACCAGG | 114792 |
| rs183428180 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121509 | TTCTAAAATTTAAAA[C/T]GTAAAGAGAAAGGTG | 114792 |
| rs183479777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912149 | CTCAGTGGTGGCCAT[C/T]ACCTCCTCCCTAGGT | 114792 |
| rs183572012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041005 | TTCCTTTATAAGTCA[C/T]CTAGTCTCAGGCAGT | 114792 |
| rs183617396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113620 | TGCTGAGACGGAAAA[A/G]AAGTTCCTCACATGG | 114792 |
| rs183661382 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079068 | TATGCAGACTCTAGG[C/T]ATAAGGCTGCATGTT | 114792 |
| rs183669619 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124246 | AGGTTTGTTAGGCAC[C/T]TCCTGTGGTTTAACA | 114792 |
| rs183719303 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97139065 | TTTATGTATACATAG[C/T]TTTATTTTGAGCAGT | 114792 |
| rs183722131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033136 | TATACTTAATAGACC[G/T]CAGTATAGTGTCAAC | 114792 |
| rs183736920 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083368 | GCATTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 114792 |
| rs183740080 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052845 | TTCACTTTTTATGCA[A/G]TGTTCTATAATATAA | 114792 |
| rs183743867 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035350 | TCTTTTAAATGTTGG[A/G]GTAAAAGTAACTTAC | 114792 |
| rs183749205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075324 | ATTACATACAGTTGT[C/T]CATACATATTTACAT | 114792 |
| rs183751346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102327 | AGCTAGGAAACAATG[A/G]GGGGTGTTGTGACCC | 114792 |
| rs183759470 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118502 | CGGGCGCCTGTAATC[G/T]CAGCTACTTGGGAGG | 114792 |
| rs183762168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996503 | TTAGAAATAAATAGG[C/T]TTTTAAAAATTCAAT | 114792 |
| rs183769296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101014 | GGCCTCCCTATGTTG[C/T]CCAGGTTAGTCTTGA | 114792 |
| rs183772021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016762 | AGCCAAATCTCATCT[C/T]GAATTGCAATCCCCA | 114792 |
| rs183785224 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138188 | TTTCCTGCTTCAAAG[A/T]TTCAGCCAGGTTCAG | 114792 |
| rs183792203 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993492 | TTTGGGTCTTGTTTG[C/G]TAATGTCCCCCCTGC | 114792 |
| rs183796746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059858 | CATTTGATGATTATA[A/C]ATTCAAGATTCTGAT | 114792 |
| rs183805350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952180 | TGCTAGGATGGGCTT[C/T]AGCCACCCAAGACCT | 114792 |
| rs183825521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025229 | TGATTTGGAACGAAT[C/T]GTCCATAGAGTGGGA | 114792 |
| rs183855052 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011649 | CATATTCAGAGTGAT[A/C]ATTTATCTTGAATTA | 114792 |
| rs183873981 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990409 | CAGTAAATGGTGCTT[A/T]AGTATAATGGTAAGT | 114792 |
| rs183881261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947521 | TGTGATTAATGTCAT[A/G]AGCAATGTCTTACAA | 114792 |
| rs183889518 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977756 | CAAAGATGCCAAAGC[A/G]TAGAAGACAGCCTTT | 114792 |
| rs183891050 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928326 | TTGGAAATGTGGGTT[A/G]AGAGGATGATGCTAG | 114792 |
| rs183892558 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038810 | GAATTGGGCTGGGTG[A/C]AGTAGCTCACACCTG | 114792 |
| rs183895238 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900581 | CTGCCTGTGCCTGAC[A/G]TTGGCCACAGAAATA | 114792 |
| rs183898799 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056991 | TTATAATAAAACTCT[A/C]TTTATACTTAAATTT | 114792 |
| rs183899199 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117895 | AACTGCAAAGTTAGT[A/G]CTTTAAAACTATAAA | 114792 |
| rs183900291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080277 | GGGACAATCAGGAAG[A/G]CCTGTGAGATATGAA | 114792 |
| rs183905610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020581 | ACCTGTTCTAAAGTC[C/T]AGAAGAAGATGGAAA | 114792 |
| rs183909474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908967 | ACTGAATGAACACTG[C/T]AGCAAAAAAGAGGGT | 114792 |
| rs183911991 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091950 | TATAATTTTTCATCA[A/T]GTTCCTGCCCTTCTT | 114792 |
| rs183923855 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985652 | GATACCCTTTCTTCC[A/G]GTTGATCGAATCAGC | 114792 |
| rs183923911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021055 | CCAATAGGTTGTATA[C/T]ATAGAGAAAAAAAGA | 114792 |
| rs183928452 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949087 | ATCACGATGTTTTGT[A/G]CATTTTAGCAGCCAT | 114792 |
| rs183928641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001034 | GACTTGAGAGAAGGA[A/G]GGATAATAGATGGAG | 114792 |
| rs183936067 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962704 | AGACCCTGTGATGTG[C/T]CAGCCTTTGCACTAG | 114792 |
| rs183937183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945383 | CCCTAAGACTGGGGC[A/T]TGCCTGTGGGGCAGG | 114792 |
| rs183952796 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050080 | TGCTGCAAGAATCAT[A/G]AAGCCATTCGTTCAG | 114792 |
| rs183959014 | snp | G/T | 0.0599851 | 0.162463 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942563 | AAGCTATGTCTTGAA[G/T]TGTTAAGGCTGGAAA | 114792 |
| rs183964709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906950 | GGCTAAAAATATGAC[A/G]TCTGTCTACAGCTCT | 114792 |
| rs183972306 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014122 | CCACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 114792 |
| rs183976595 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980511 | TTTCAAGTATAAAGC[C/T]TACTTGATTGTGGTG | 114792 |
| rs183977338 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080456 | TGGATACCAGGGACA[C/T]ACAAGGCATGAGACA | 114792 |
| rs183979509 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097456 | GGCTACACTGAGGTA[A/C]ATGAGAACGTGCAGT | 114792 |
| rs183992280 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115035 | GTTGTTGCTGTTTCA[A/G]ATAGGGTCTCACTCT | 114792 |
| rs184013421 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057645 | TTTGGATAACATTCC[A/T]TTAGCAGATGTATCT | 114792 |
| rs184024745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903410 | ATAGAATAGATTACG[A/G]TCACTCTCATGATTA | 114792 |
| rs184055754 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96999496 | TGTACTCATCTGTTT[C/T]CACCATATTTGATGG | 114792 |
| rs184109661 | snp | C/T | 3.32022e-05 | 0.00407431 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976065 | ACAGTGTCCTGGCAG[C/T]GCTGAATCAGCAGAG | 114792 |
| rs184118536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927412 | TGGGAACTCAGAGAC[A/G]TTAAATCCCAGCACC | 114792 |
| rs184181708 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956797 | CATGTACATACATAC[A/G]CCTAGCCCATATGTA | 114792 |
| rs184198357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934125 | ATTGTAGGACCTTGC[A/G]TCAGAAAATCATATA | 114792 |
| rs184248586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093827 | CAGGAAATGAAAGCC[A/G]ATAAGGGAGGATCTC | 114792 |
| rs184275014 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107137 | CTCTTACTAAAAATA[A/C]AAAAAATTAGCTGGG | 114792 |
| rs184280949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123944 | CATATCTATTTTTGT[A/G]TAGTCAAATCTGTAT | 114792 |
| rs184291864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066925 | GCTTAAAATGTACCC[A/G]GGAATTGTGCCCCTT | 114792 |
| rs184293185 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128522 | TGGCATATTGTTTAC[G/T]GTGGGTACTGGCAAA | 114792 |
| rs184302214 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089680 | GCTGAGGCCTGGAGG[C/G]TGAGATAGGAGAATC | 114792 |
| rs184315645 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012145 | CTGTTCATGTCTGCC[A/G]TTAGCTATTGAGCAT | 114792 |
| rs184326218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047752 | GTCAGCCACCCAGGA[A/G]CAGGCAGGTGTTTTT | 114792 |
| rs184327728 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030892 | TGCAGATGAGTTTTG[A/T]AGATGATATTGGTTG | 114792 |
| rs184331222 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135223 | ATTCTGATGAACAGA[A/G]TCAATCCTTTGGCAA | 114792 |
| rs184331845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026269 | GTTTGCAGAAAAAGT[A/G]AGCTTGATGGGAGGA | 114792 |
| rs184339927 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061080 | GCACTGTCCAACATC[C/G]CTCATTCGAGAACAG | 114792 |
| rs184413903 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111035 | AGAAAAGTCTTGGGG[C/G]GGGGGGGTCTTAGCC | 114792 |
| rs184427083 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026829 | CTGAGGAAATTCCAC[A/C]CTATTATCTTCAACA | 114792 |
| rs184436208 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048617 | CTTTTTTTATATAGC[C/T]CTGATAATGCAAACA | 114792 |
| rs184440650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114800 | TCCTGTCAGCTCTTG[A/T]TTATTCATGGATTGT | 114792 |
| rs184446434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089939 | CAAACAAGGTAAGAC[C/T]TCAGCAGGGAGGGTT | 114792 |
| rs184449180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987706 | GACTTCAAACTATAC[C/T]GCAAGGCTACAGTAA | 114792 |
| rs184451732 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041944 | ATCATGGCTTTATTG[A/C]CTTAAAAACAAGACA | 114792 |
| rs184459841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006724 | TTGCTTGTCTGAAAA[C/G]GATCTTATTTCTCCT | 114792 |
| rs184464291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970702 | AAAACTATTCATTCA[C/T]AATTAAGTTCCTTTC | 114792 |
| rs184471196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925487 | AAAAGGATTCGTCAG[A/T]TGAATTTTTCAACGG | 114792 |
| rs184472795 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943631 | CCAGGACCCAGGTCT[C/G]CGAGGTCTTGTCTTT | 114792 |
| rs184477014 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903785 | CTAAAAATACATTTA[G/T]CTAACAGGGAATAGA | 114792 |
| rs184483030 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978422 | TTCCCATGTTAGTTA[A/C/G/T]CTTAGAATAATGGCC | 114792 |
| rs184521544 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936445 | CCTCATCCAGAGCCT[C/T]TCCATTTTTGGTTGT | 114792 |
| rs184525333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900190 | GTTGAACACACTTTG[C/T]TCATCTTAAAATTGG | 114792 |
| rs184526728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062001 | CCAACCCTTTAAGAG[C/T]ACTTAGAGATTTTCT | 114792 |
| rs184533280 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084988 | ATAATTGTGATTTCT[C/T]TTTTTTTTTATACTA | 114792 |
| rs184533651 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127866 | CTAAAGTAGAAGTAT[A/G]TGAAGAATCTGAGAG | 114792 |
| rs184535297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103417 | ATGGGGTTTCACCAT[A/G]TTAGCCAGGATGGTC | 114792 |
| rs184557088 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042421 | AGTACACAATTTTAC[A/G]GATAGGGTGGTATTT | 114792 |
| rs184560844 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129940 | CCAAAACAAATAAAT[A/G]TGTGCCTAGAAATAA | 114792 |
| rs184561512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027643 | TTCACAAGCTTAGGA[C/T]GATTTACTCTTTCAA | 114792 |
| rs184566591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097127 | AGGGAGGGAAAAAAA[A/C]CACGCAAATTTAAGA | 114792 |
| rs184573606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068355 | CCACCAAAGTACTGA[A/C]TACGCAACTCCCTTT | 114792 |
| rs184576074 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134825 | ATTTTGTTAACAGTC[A/C/G]TGAATGTTAGTTTGT | 114792 |
| rs184579007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039143 | AATTAACTAAGTGCT[C/T]ATCAGTGAATGAATG | 114792 |
| rs184583515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065906 | GGTCAGCCATGTTCA[C/T]CTGAGGAAAATTCAA | 114792 |
| rs184588705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991388 | CCGTATGGTGGCTGG[A/G]TGTGCTAGGGATGTC | 114792 |
| rs184597817 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031863 | TGAGTGGAGGGTGCT[A/G]TTTCTCAGCTCTCGT | 114792 |
| rs184612292 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963677 | GCTGAACTGAGAGGC[G/T]GATGGATACTTAAAA | 114792 |
| rs184618687 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001761 | ATTAGGTCTTAGTGT[C/G]AAAGTTGAGTGATTC | 114792 |
| rs184649260 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919551 | AGTTTCCAATTTTGC[C/T]TGATTAATTTTAGGA | 114792 |
| rs184714048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089467 | TACTTTTAGTGAGAA[C/G]TTATTATTTTGTAAG | 114792 |
| rs184717430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021687 | AAATTAACCACCAGA[A/G]ATGATGACTGACAAA | 114792 |
| rs184748920 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047166 | ATTTTAAAGAAAAAG[C/G]AAATTTTCCTCTTAA | 114792 |
| rs184755087 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985889 | GTCAAAGTCATTCTC[C/T]GTCCAGCTTTGTTCC | 114792 |
| rs184757971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938409 | GGGCTGGGCCCCACA[G/T]TGGACACCTTCTCTT | 114792 |
| rs184786183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956421 | AGAACCCACTCTTCT[A/T]ACCTGTATACTATGC | 114792 |
| rs184787498 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916283 | GATATTGTTATAGGC[A/C]CATACTCCTAAGTTA | 114792 |
| rs184794774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933714 | TCATCTCCCAGGAGC[C/T]AGCCACATGTCCCTC | 114792 |
| rs184796142 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942763 | GAAAGCATAGAGAGA[C/T]TGAAAAAGACTTTCC | 114792 |
| rs184825859 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915633 | AAATTCAATAAATTG[A/G]TAAGTTTCTATCCAT | 114792 |
| rs184864095 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120442 | GGTGTTCAGAATCCA[A/C]ACTAACCTTGGAAAC | 114792 |
| rs184897841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969184 | CAATCTGCTTATCTC[C/G]AAAGACCATCTCCCT | 114792 |
| rs184902656 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005823 | TAATGTCTTTTCTAT[C/G]AGACTGTGCTCTGAG | 114792 |
| rs184929052 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925223 | CTGGAGTCGCTCCCC[C/T]TTTCTTCCCTCCCCC | 114792 |
| rs184959399 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935630 | TTGGCCATCTGTGCC[A/C]AATTATAGGGAGTAA | 114792 |
| rs184970659 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899001 | CGAATAGAATAATAA[C/T]AATAAAACAAGAATC | 114792 |
| rs184970822 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919358 | TTGTCACTATGATTA[A/C]AGAGAACGGGAAAGG | 114792 |
| rs184985559 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077837 | TGTTGCAATCTATGA[G/T]AAAGACATTATGATT | 114792 |
| rs184985974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104349 | CACCTTTAGTTGCAA[A/G]GGCTTTTCGCTTTTG | 114792 |
| rs184987918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056060 | GTGACCTCACAGCTT[C/T]GTGCAGCATAGCCAG | 114792 |
| rs184992258 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120660 | TTTGCTTGAGGGAGA[A/G/T]AAGTGTGTGTTGCGG | 114792 |
| rs184996400 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096221 | TTCTGAGCCAACAGC[C/T]GTCCTGTCCTCTGTC | 114792 |
| rs185012368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019215 | AAAAAAGCAGCGTTC[G/T]TAATATGGACTTGAA | 114792 |
| rs185028897 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036224 | CTTTCCCTTTCATTT[A/T]TGTATTACATAAAAT | 114792 |
| rs185044885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998613 | AATTAAATATCATGA[G/T]GTTCAATATTTTCCT | 114792 |
| rs185078494 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135578 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCATCT | 114792 |
| rs185108345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098325 | ATATATTAGGCACCT[A/G]AGAGCTAGAATCGTT | 114792 |
| rs185133136 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081550 | ACATCCCCATCCCAC[A/C]CTTTGCCAAGTGAAC | 114792 |
| rs185138808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058915 | ACATATAGACACACA[C/G]AATTGTAATGATACA | 114792 |
| rs185149971 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099405 | CTCTTCCTCCTAATC[A/T]GATAAAGAATGTTTC | 114792 |
| rs185151810 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023725 | CCAGCTGGCCTAGTT[A/C]TACATGGATAGTATC | 114792 |
| rs185161172 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002744 | GGTTTTCTGTTCCTG[C/T]GTTAGTTCACTTACA | 114792 |
| rs185165444 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040289 | CAAAGATTAAAGGTG[C/T]ACAAATTAGCATGGG | 114792 |
| rs185179175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986515 | TGAGCTGTGGTGGGC[A/T]CCACCCAATTCGAGC | 114792 |
| rs185221850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119142 | CTGCTTGTTCTGTCC[C/T]TGTACCTAGGTGGCT | 114792 |
| rs185230886 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115683 | GTTTTGAGAAAGGCC[C/T]TAAGTGTTCTCCTTT | 114792 |
| rs185252447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083995 | TGTGTGCTATGTTGT[C/G]ATTGCCTTGGGGTGA | 114792 |
| rs185292218 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042353 | GGAGTTATAACAGAA[A/G]CAGAATACAAAACAG | 114792 |
| rs185298072 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015587 | GATGTGAAATTGGAA[A/C]CTATGTTTAAAAGGG | 114792 |
| rs185321916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982064 | GTAGATATCTGTTAG[A/G]CCCATTCAGTCAAGT | 114792 |
| rs185343548 | snp | A/C | 0.00557542 | 0.0525036 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141318 | AAAACAAATCAGCAT[A/C]TATTAAACCCCTCCT | 114792 |
| rs185350466 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933180 | GCCTTTGAAAACAAC[A/G]ACATATTTTACTCCT | 114792 |
| rs185365823 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061542 | CCTGTGTGCTTTCAG[A/G]TCTTGGGGAACATCT | 114792 |
| rs185373874 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103171 | TTAAAGACAGTCCAG[A/G/T]GGTAAAATATATGTG | 114792 |
| rs185378488 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110874 | GTTGTGGCAATTCAC[A/G]TTGTTCTGAATTGCT | 114792 |
| rs185410113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073700 | TATCCTATGCTTCCT[A/G]ACTAGGGAACATAAA | 114792 |
| rs185417846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995931 | TGTGACCAACTAAAC[A/T]CTAGTGAAGTCCACC | 114792 |
| rs185425519 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034896 | CTAACATTGTTTTTT[C/G]GTTGAATCTTCAGGG | 114792 |
| rs185426105 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995195 | TCAATAAATGTGAGC[C/T]GTTTCACTTCTTGGA | 114792 |
| rs185454256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929907 | TTGCAAGGTTGGAGT[C/T]ACCAACCTGATAAGA | 114792 |
| rs185457653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954399 | CACTCATATTAAAGA[G/T]AAAAAAAACTGGCTG | 114792 |
| rs185460563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911088 | GTTTTCTAGGGTTGC[C/T]GTAACAAAGTACCAC | 114792 |
| rs185464128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914649 | TCACTGTATCCCATG[A/T]TCCCAGCACTTACAT | 114792 |
| rs185508022 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048678 | CTGTATTCCCCACAG[A/C]AGAATACTTTTCTCG | 114792 |
| rs185515750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052401 | AAACAAAGTAACAGT[C/T]TTCTCTTTGTTTTTA | 114792 |
| rs185516630 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032439 | CTCTACTAACTCTCT[G/T]ATGAGGATCCCTATT | 114792 |
| rs185531672 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093795 | TCCTTCAAAGTACAC[A/G]ATGGTGTAGTATAAA | 114792 |
| rs185536892 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992336 | CTCCCCTGGCTCTTC[A/G]CCTCTCCCCGGTGGG | 114792 |
| rs185553206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013202 | ATATGTGTAAAGTTG[C/T]ACATCATAGAAGATG | 114792 |
| rs185555749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950220 | GTGTCTGAAATTTCT[A/G]CATTTGTGTTAAAAA | 114792 |
| rs185562273 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016134 | GGGAAATGTGGGGTC[A/G]GAGCCCCCACACAGA | 114792 |
| rs185566033 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990849 | AAGATGGCTGTGGTT[G/T]CTGGAGGTGTAGGTA | 114792 |
| rs185568846 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978792 | CTCTTTTCTCTGCAA[A/C]CTCTCCATCATCTGC | 114792 |
| rs185569441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982735 | ACATTGATTTTGTAT[C/G]CTGAGATGCTGCTGA | 114792 |
| rs185570492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948305 | ACCTTGTACGTCAAA[C/T]TTGAGGTTGGTTCAT | 114792 |
| rs185578742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930095 | CAGATGATACAACCC[A/G]TTTGTTATACAAGAT | 114792 |
| rs185584324 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909861 | GAATGTCAGCAGTTG[A/T]GTCCTGCTGGTATTG | 114792 |
| rs185623004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902772 | TTTCTGTGTATGGTG[G/T]AAGGAAGGGGTCCAG | 114792 |
| rs185623448 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100262 | GATGAAATGAAGTTA[C/G]AGAAGGCAGTGCAAA | 114792 |
| rs185635334 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137552 | GTCTTTTTTTTTCCC[C/G]CAGACGGAGTATCAC | 114792 |
| rs185658757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081959 | AAGATCGCAGTGCCC[C/T]GGTCATGGAAGGCTA | 114792 |
| rs185704719 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906007 | AGCTCTGCCTTTTTA[A/T]TCTGGTAGTCCCACC | 114792 |
| rs185711157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926555 | AGTGAATGGGGAAGC[C/G]CTTTCTGGATCCAGT | 114792 |
| rs185719112 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929630 | TGTCAAGATCTTTAC[C/T]TAAGAGGAGCTGAGC | 114792 |
| rs185745164 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141948 | ATACTTTTTCCTTCA[A/T]ATTTTCTTCACACTT | 114792 |
| rs185839647 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132456 | TTTGGCCTGGTTCTG[A/C]CCTGACAGATTCATT | 114792 |
| rs185845077 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986220 | ATGTTGCTGCCGGAT[C/T]GTTCCTCTGGAATTT | 114792 |
| rs185857637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002158 | CCAGTCTGAGTATAA[A/G]TCCAAAGGTAGGATA | 114792 |
| rs185858565 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022518 | CTTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTGCG | 114792 |
| rs185859355 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965555 | ACACTGGACTTTCAG[A/G]AAGATTAAGGTGTTA | 114792 |
| rs185882604 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062106 | AAGACAAAAACAATC[A/G]CCGTATGGGTTTTTC | 114792 |
| rs185918693 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989006 | TATACCTAATGTTAA[A/T]TGAGAAGTTAATGGG | 114792 |
| rs185926923 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027975 | AGAAAGCTATCAAGA[A/G]GGTGATTGGAAGTCA | 114792 |
| rs185949641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944554 | TGATGCTATATATTC[A/G]TATTGTACTTCATAG | 114792 |
| rs185962075 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126164 | ATATCTTTATTGAAA[A/G]ATTAGCTGCTTCTTT | 114792 |
| rs185981412 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116676 | ATGACGATTTAATAC[C/G]TTCTTCAGTGAGGCC | 114792 |
| rs185987361 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092360 | CTGGGTATCTTCATA[A/G]TATCTCCTATTTTTT | 114792 |
| rs186008545 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091139 | ACCTGAGCCCAAGAA[A/G]TTGAGGCTGCAGTGT | 114792 |
| rs186014856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109641 | AGATAAAGATAAACC[A/G]GAGGGTGTTCAGAGA | 114792 |
| rs186016263 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043243 | CCTCCCCTAGCCTTT[A/G]GTAACCATCATTCTA | 114792 |
| rs186019161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125751 | ATTGCACTCCAGCCT[A/G]GGCAACAAAAGCGAG | 114792 |
| rs186019372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050269 | GGCAGAAATAGAATG[C/T]GCAACCCCCCAACCC | 114792 |
| rs186028781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032663 | CGTCAGCACATCAGG[C/G]GCAATTACAACTTGG | 114792 |
| rs186033507 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086191 | AGACTACCAGGGAAA[A/T]TTTAAAGTCTTCTAT | 114792 |
| rs186037002 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070263 | ATTATTTTTAATCAG[A/C/T]GAAAATGATCAAAAA | 114792 |
| rs186037225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007679 | TTTTCATCTTTGATA[A/C]CCTTGGGAGTTTGAT | 114792 |
| rs186042806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049758 | TTTGCTTTTTTAGAT[A/C]TTTTGAAACTAGTTA | 114792 |
| rs186064177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974227 | TCATGGGACACGGTA[A/G]GCACTATGTGTTTCT | 114792 |
| rs186070143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939650 | CAGTGTCAACACAGT[C/G]GGGTGCAGAGAGCCA | 114792 |
| rs186091703 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901416 | TTGCATCACTTCATT[A/G]TCACATTTCCTTCTC | 114792 |
| rs186094920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007172 | TATCCCATATTTCTT[A/G]GAGGTTTTGCTCATT | 114792 |
| rs186097372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958951 | CGTCTACACTTTGGA[C/T]CCTCATCCCTCTCTG | 114792 |
| rs186103250 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997971 | CATTACCATTTCTGC[G/T]TCTCAGAAATCACAT | 114792 |
| rs186109511 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983937 | CTTTTGAATGTGTTT[G/T]CTCTTGCTTCTCTAG | 114792 |
| rs186113331 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934508 | AGTGCTCTCCAGATA[A/C]TCAGTGGACATTTAA | 114792 |
| rs186118705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071435 | TAGCTCCTTGACTGT[A/C]CCTCAAAGCATGGGA | 114792 |
| rs186124801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136605 | TAAAGGAGCAGCTGC[A/G]TAAGTGTGCAAGTGA | 114792 |
| rs186130062 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896255 | CATAGGTTCCCATTC[C/G]TAATGTATTCTTTGA | 114792 |
| rs186131688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917319 | CCCTGATCTCTCTGC[C/T]TGATATCCTCACTGT | 114792 |
| rs186132854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109854 | AAGAAATTGGTTGCA[A/G]AGCAAAGCAATATCA | 114792 |
| rs186145105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043900 | TTGATTGGGTTATTT[A/C]TTTTCTCATCTTCTT | 114792 |
| rs186149314 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075613 | TTTTGTTTATTTATT[G/T]GTTTGTTTCAACCTG | 114792 |
| rs186153326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094993 | CACTTTAAAACAAGT[G/T]AGCATAATATCATTA | 114792 |
| rs186158266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003251 | CTCAAATGATTAATG[A/G]TGATGAACATTTTTT | 114792 |
| rs186168596 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040725 | AGTCCCTATAATCCC[A/C]ACATGTCAAGGGAGA | 114792 |
| rs186177250 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069654 | CCCTCCCTCCCTTCA[C/T]ATCGTGGGAGTTCAT | 114792 |
| rs186177556 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967712 | TGTATATTCTATGGC[A/G]AAAACAGACATTAAA | 114792 |
| rs186179987 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028144 | TCTCAAACATTTATG[C/G/T]GCATGTGGTTCACCT | 114792 |
| rs186184089 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989101 | CTAAAATTTAAAGTA[C/T]AATAAAAAAAATATT | 114792 |
| rs186187076 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007927 | CCACTAAATTACTTC[A/C]TCAAGGTGTTGGCAG | 114792 |
| rs186189108 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053038 | TTTGATGCTAGGAAG[C/T]ATAGAGCCACATTGT | 114792 |
| rs186193002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945341 | AAACCACATCCAACT[C/G]CCTTAGAGCAGAAAT | 114792 |
| rs186203788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927279 | ATAGGAAGACGTAGG[A/G]TTGGTCAGCAAATGG | 114792 |
| rs186209375 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967398 | ATAAAAAAGGAATCA[A/T]AAAACTATACATATA | 114792 |
| rs186209630 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923010 | TGAGCCGATACTATG[C/T]GGCAGACATTGTGCT | 114792 |
| rs186268682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938811 | CTGCAGTATAATCAT[G/T]TGACCCACATGCAGT | 114792 |
| rs186274712 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922652 | TTGCTGAACAAATAA[C/T]AAGTATTCCAAAAAA | 114792 |
| rs186276846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900801 | AACCACTAGTGAGGA[A/G]CACAACAGATTTATG | 114792 |
| rs186321258 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025203 | TTCTGTTTATCGTCT[C/T]TGTAAAAATCTGATT | 114792 |
| rs186342176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940933 | ACACAGGCACAAATT[G/T]TTGGAATTCAGAGAA | 114792 |
| rs186395154 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911741 | GGTCTTTTTCTTACT[C/T]ATTACTCAGCAGTAT | 114792 |
| rs186522014 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109182 | GTGTAATTTGTGTAC[A/G]TGTTAAGTTTGTAGT | 114792 |
| rs186569163 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121650 | GTTTTGTTTTGTTTT[G/T]TTTAATGTCCAAATC | 114792 |
| rs186612034 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976937 | AATTATTTGCTCCAA[A/G]GACAGAGATTCATAG | 114792 |
| rs186616610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927824 | GTGCATGGAGATACC[A/G]TCTCTGCCCTCAATG | 114792 |
| rs186621647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947435 | CATGTTAGGAACATC[A/G]ATACAATTTATTTCT | 114792 |
| rs186624281 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908452 | GAATGTTATTAACAG[G/T]GTTCTGCCACATGCA | 114792 |
| rs186652054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122719 | CTGTGGATTGTCTCT[A/G]TGCTTTGCACTCTAG | 114792 |
| rs186657992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097234 | TGATTAGGCCTGGTG[C/T]GGTTTCATCAGACTC | 114792 |
| rs186659942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114812 | TTGATTATTCATGGA[C/T]TGTATTGCACAGCTT | 114792 |
| rs186711814 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022260 | TCATCCCTCCTACAA[C/T]TCTCAACCTCCGTCC | 114792 |
| rs186722938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058234 | TTTTGGGTCTTTTGC[C/T]TCTTCATATAAGCTT | 114792 |
| rs186729554 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993110 | AGACATAGGCTGAGC[C/G]CTATGGAGCTTGTAA | 114792 |
| rs186732521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952389 | TTATGAATTAGCCTA[C/T]GGTAAAATTGAAACT | 114792 |
| rs186738018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980692 | AAAGACATAGAGAAG[A/G]GTTTTTCTTCCTTAG | 114792 |
| rs186740375 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951291 | GATGTCAACAGCCCT[A/C]TACACCTTGTTCCTG | 114792 |
| rs186741336 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059264 | CATTGAAGATGGAGA[A/G]CAAGGTATTGCCTGA | 114792 |
| rs186741492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090494 | ATTAATCATTTTCTT[C/G]AAAAGGAGTCCCAGA | 114792 |
| rs186749482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912453 | AGCACCCATTGTGAT[A/T]TTTCCTGTGTTGCTC | 114792 |
| rs186760132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124703 | TGGAGCTTTGCCCTC[A/G]GTTCCATTTCAGTTA | 114792 |
| rs186763804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913611 | AGTCTAGATGGGTCG[A/G]TAGGGAGACTAGGTG | 114792 |
| rs186798429 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082917 | GCTTCATTTTGACCT[C/G]TTTGCATCAGTGATT | 114792 |
| rs186799047 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121337 | AAGAACTTCCAAATG[G/T]CATAAAACTGAAAGT | 114792 |
| rs186801128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101444 | ATGGCAAATGAGAAC[A/G]TTGATATACACTGAT | 114792 |
| rs186818003 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041819 | TAGTATTTTAAATTT[A/C]ACTCAGTGCTTGCTG | 114792 |
| rs186823340 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026082 | TTATATAAATTTTGA[A/G]AAATAAATACATTAT | 114792 |
| rs186828095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981518 | TCCTAGTTCCATTGA[C/T]CTTTTATATGATTTT | 114792 |
| rs186833718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060503 | GTGGGCACTGACTGA[G/T]GTGGCCCACGTCATC | 114792 |
| rs186836979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086829 | GTCAATTCAAAATGG[A/G]AAGTAGTCAAATTTT | 114792 |
| rs186838686 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994388 | TCAATTCTTAATATC[C/T]GGAAAATAAAACTAT | 114792 |
| rs186841626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953499 | GCCGGGTGTGGTGGC[A/G]CATAACTGTAATCCA | 114792 |
| rs186862559 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005302 | CTGAGGGTATTTTGC[A/C]TATCTGTGGGGTCAG | 114792 |
| rs186890986 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017402 | ATCATTGGGAGAGTT[A/G]CTGCCCTTCTCTAAC | 114792 |
| rs186896298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983712 | AGTTTGTATTTCTGT[A/G]GGATCGGTGGTGATA | 114792 |
| rs186906740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934334 | GATAGGTCTACTTTG[A/G]GAGATGTGGTCTAGA | 114792 |
| rs186933389 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980083 | CTATGTGGAGAGTTC[C/T]AAGTATGGAATCACA | 114792 |
| rs186934534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014032 | TCTTTTTTGGCCGGG[C/T]GCCGTGGCTCACGCT | 114792 |
| rs186937346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039543 | TAGCTAGAAGACAGC[C/T]GGGCGCAGTGGTTCA | 114792 |
| rs186964976 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931208 | TAGTTAAATCTATGT[C/T]TTTTTCTTTTTCTCT | 114792 |
| rs186984778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036065 | TGGATAATTTTAAAC[A/G]ACCAGTATTCAAGTT | 114792 |
| rs187006077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104672 | CAGCTATAATGGTTA[A/C]TGTGCAATCTCCCTT | 114792 |
| rs187035762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901762 | CCAACAGGCTCCAGT[A/G]TTTGTTGTTCCCCCT | 114792 |
| rs187037421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062599 | TTATAAAATTAGTTA[A/G]AATTGATTCTGAATA | 114792 |
| rs187038414 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923478 | GGACTGCTAGATAAG[A/T]AGGTACCCAGCATCC | 114792 |
| rs187042961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035525 | AAAATAGGTCTAGGA[A/G]TGACAAACTCTCTCA | 114792 |
| rs187070401 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926440 | AGCACTTTTCATATA[C/G]TTCTTTTTTAATCCT | 114792 |
| rs187096525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996893 | AATAATTCACATTAG[A/G]GGCATGAAAAGTGGT | 114792 |
| rs187112624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957807 | TCATGAGGGTGACTA[C/G]ATACCTTATCCTTAT | 114792 |
| rs187158137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071851 | CAATAACTCAGCTGC[A/G]CTCCCTGCCTGTAGT | 114792 |
| rs187180895 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015520 | AGCAAAGAGACTGTC[A/G]GCATTTTGCCCCTGC | 114792 |
| rs187186967 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051039 | AAAAAACACATGTGT[G/T]TGAACAATATTCTTA | 114792 |
| rs187192044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033754 | TCATTGTGGTTTTTA[C/T]TTGCTTTTCCCTGAT | 114792 |
| rs187196824 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018393 | GTAGTTTGAGACCAG[C/T]CTGGCCAACATGGTG | 114792 |
| rs187202699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053719 | GATATAAGTACATTT[G/T]TTTTTTTTAATTTAT | 114792 |
| rs187240584 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988213 | TACTCATCTGATAAA[A/G]GGCTAATATCCAGAA | 114792 |
| rs187243657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944137 | GGGAGCAACTGGAAT[C/T]AGATGCCTGTGATTA | 114792 |
| rs187247690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110556 | AGTGATTCTTTTCAC[C/T]GGGTTGAAAACCCAG | 114792 |
| rs187260048 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127272 | TTCTTAATTATGTCA[C/T]GGGCTCACCATGAGG | 114792 |
| rs187267570 | snp | A/T | | | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139123 | TCCTCTTTTGTAGGT[A/T]CTGGATGTAAGCAGA | 114792 |
| rs187268177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905212 | GATGCAAAGAACAAG[A/C]AAATACTCAAGAAAT | 114792 |
| rs187271095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072594 | CAATTTACTACCCAT[A/G]TGCAATGCCTGTTCC | 114792 |
| rs187275387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052159 | CCTTTATATTTCAGT[A/G]TGTACATGCTGGGGT | 114792 |
| rs187283692 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093368 | AAGGTTGATAAGGCA[A/G]GTATGATCCAAATTT | 114792 |
| rs187309856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118568 | AGGTTGCAGTGAGGC[A/G]AGGTCACACCACTGC | 114792 |
| rs187372375 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113104 | CTCTAACAAATTTCC[A/G]GTATCTTACATGTGC | 114792 |
| rs187372602 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066253 | ATGCTGACACAGTTT[A/G]GTTAGAGCGTTAGTT | 114792 |
| rs187399153 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029508 | TTAGTTTGTCTTGTG[A/C]TATTTTATTCTCTGA | 114792 |
| rs187402045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011860 | AGGAAGGTAAACTGG[C/T]GTTTATTAAAAATCT | 114792 |
| rs187404410 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047290 | ATGCCCTTCTTCTGG[A/G]CACACTGTGTTTGGG | 114792 |
| rs187409495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076994 | TCTTGCCTACCCACT[G/T]TATATCAATCAAAAC | 114792 |
| rs187416475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111679 | CTTAAATATTAACAG[C/G]TCAGTGGAGGGTCAC | 114792 |
| rs187419490 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078685 | ATTCTCAGAACTAGA[A/C/T]GAGACAGCAAGAGAA | 114792 |
| rs187419721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096608 | AGAATTTTTAATTCC[C/T]TTTCCCCAGATATTC | 114792 |
| rs187422650 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945741 | TTCAGAGAAGTGGGT[A/G]GTAGCTTCCCGGGGG | 114792 |
| rs187427984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990566 | AGGGTGCACACTGCA[A/G]CTCTGGGGTGAGCTC | 114792 |
| rs187441391 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977792 | AAAGCGTATTAAATG[A/T]GATGAAACTGAGTAA | 114792 |
| rs187452209 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135030 | TTTAAACCACTGAGG[A/G]TATTTGAGAGTATCC | 114792 |
| rs187456549 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004887 | TTATTAGTATTTTGT[G/T]GTGGATTTTTGCATC | 114792 |
| rs187468637 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986949 | ATGCAGAAATCACCT[A/G]TCTTCTGCATCGCTC | 114792 |
| rs187470442 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025735 | ATGGGTTCAAGTCCC[A/G]ACTCTCCCTCTTACC | 114792 |
| rs187486410 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967991 | CAGTCAAAATATCTT[A/C]AGAGCAAAGAATAAG | 114792 |
| rs187492338 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924024 | TATTGCTGAATTAGT[A/G]GTAACCACAGTAATC | 114792 |
| rs187494929 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942368 | ATCTGTGCATCAAGC[C/T]ATCTGTGCTCAATAC | 114792 |
| rs187498859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902592 | GAGCTCTTTAGTTTA[A/G]TTAGATCCCATTTGC | 114792 |
| rs187504065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065193 | CCAGGCAGTAAATGC[C/T]GGAGAAGGGATGAGT | 114792 |
| rs187523316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029182 | CAGGTCGTTGAAACA[C/T]GGCCACATTCAAGAG | 114792 |
| rs187540424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990341 | TCCTTGTTTTTATGG[A/G]GGTGGGGGTTATGTT | 114792 |
| rs187573757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960166 | TTTAATTAAGGTTTT[A/G]TCATCTTCATCATTA | 114792 |
| rs187578491 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918153 | ACGGAAAGAGCTGCT[C/G]TCCAAGGCAGCCATG | 114792 |
| rs187613845 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898720 | CAAACAAACAAAAAA[A/T]CGAGTGTTACATTCA | 114792 |
| rs187633096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130133 | GGCCTGAGGTACCCA[A/G]TGATTATCATCACAT | 114792 |
| rs187646516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014877 | ATGGTTAGGCTCTGT[A/G]TCCCCACCCAAATCT | 114792 |
| rs187655438 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987169 | AAACCAGCTCCTGGA[C/T]TCATTGATTTTTTGA | 114792 |
| rs187664123 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942564 | AGCTATGTCTTGAAG[C/T]GTTAAGGCTGGAAAG | 114792 |
| rs187670293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095837 | GTTTGAACCATTTCC[C/T]AGATAGCTTTCTTTG | 114792 |
| rs187686696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903035 | CATGTTGCCGCCAGC[C/T]TTTTTCTTTCTGTTT | 114792 |
| rs187691893 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961969 | AAGCACCGTTACTAC[C/T]GTGACCCATAGTCAG | 114792 |
| rs187711548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936239 | GGATTTTAAATAGAC[A/G]TGTCTACATTTTGCA | 114792 |
| rs187717743 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919472 | ATATGTATTCATATG[G/T]GTTTCATTTGTTTGT | 114792 |
| rs187720416 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899140 | CACTCTAATTTAAAT[A/G]CCCTTTATTTAATTA | 114792 |
| rs187757265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088770 | CCAAAACATGGCAAT[C/T]CTTCATAAAAAAAAC | 114792 |
| rs187791450 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046267 | ACCCCACTTGAAAGA[A/T]GACAGGCCCAGGGAA | 114792 |
| rs187806209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011045 | CTAGATGGTAAATGA[C/G]AGCTTCCCAGTGGAC | 114792 |
| rs187818421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932950 | GCAATTAATTATTGT[C/T]ATTACATTTTGTTAA | 114792 |
| rs187851206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934947 | GTTTCAAATTGTAGC[C/T]TGATCTTTATTTTTG | 114792 |
| rs187870932 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138564 | AAACAACAAAAAAAC[A/C]CCAAAAACAAACAAA | 114792 |
| rs187916799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033174 | TTATATGTACTGGGA[A/G]ACCAAAACATATGTC | 114792 |
| rs187951240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968929 | CTTCTAGACCATTAC[A/T]CCACAAATTGATTGT | 114792 |
| rs187958794 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123856 | TGATGACTTTCAAAG[A/C]CAGGAATACTGCTGC | 114792 |
| rs187961430 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993499 | CTTGTTTGCTAATGT[C/T]CCCCCTGCTGGCCGA | 114792 |
| rs187965468 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924882 | GTCTTCGCTACTGCA[C/T]CCCCGAACCAGCAGA | 114792 |
| rs188043425 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087702 | GTAAACACACACACA[C/T]TTACGCAGGTGGCTC | 114792 |
| rs188056843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106228 | ATAATTGATATATTT[C/G]TGAAATACATATGAT | 114792 |
| rs188067230 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000253 | TAAGGGTGTTATATA[A/C]AACTATTAATTGATG | 114792 |
| rs188078574 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063322 | TGGATTCGATATAAG[C/G]CCTAAGGAAAACAAG | 114792 |
| rs188078743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985076 | GGCCTGGTGGTGACA[A/G]AATCTCTCAGTATTT | 114792 |
| rs188084955 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020747 | GTCACTTCCTATTTC[C/T]TCCTTGAAACATTTT | 114792 |
| rs188108751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913934 | GATGGAATTAATGTT[A/G]TAAATCAGCTAGCTT | 114792 |
| rs188116422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083809 | ATCCACCGTACTATT[G/T]TTGGGCATTTAATGA | 114792 |
| rs188146858 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041976 | AAAATTTAGATCCCC[A/C]AAAATTTATGTCCAA | 114792 |
| rs188146877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110232 | CATAGATAATTTTTT[A/G]TCAGGTTGGTATCTT | 114792 |
| rs188164304 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038952 | AAAATTAGCTGGGTA[C/T]GGTGGCACGTGCCTG | 114792 |
| rs188170318 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991588 | CGCCCAGGTGGAGAG[A/G]TCCTGCCCATTGAGG | 114792 |
| rs188171504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042680 | CAATGTTGAACTATA[C/T]AATGCATTATTATTT | 114792 |
| rs188180956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027825 | TGGCTTCAAGCACTA[A/T]CATTTTATGACTCCG | 114792 |
| rs188182358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080388 | AAGTAAACAGAAAAA[A/G]CTCATGGGTATTCTT | 114792 |
| rs188182646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057077 | GGACTGTTTTAAAAA[G/T]TTAAAACTATTTTTA | 114792 |
| rs188197133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978499 | TTATGACTGTGTAGT[A/G]TTCCACAATATATAC | 114792 |
| rs188201247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021363 | ACCCAGGAGAGCCGA[C/T]GATGTAGTTTCTGTT | 114792 |
| rs188201429 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929962 | TCTTTGGCAGTTTTC[A/C/G]TGGACTCTTGACAAC | 114792 |
| rs188209721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949237 | CATAGTAGGAATTAA[C/T]AACTTTTCAAATGGA | 114792 |
| rs188212547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001165 | AGGAGTGAACCCTAA[C/T]GTAAACTTTGGATTT | 114792 |
| rs188223943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911393 | TCAAGCATTTTCAAC[A/T]TCCCCCCATGGTTCT | 114792 |
| rs188253680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101108 | CCACTGCATTCAGCC[A/G]AGCTCATTATTCTTG | 114792 |
| rs188277060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138225 | GACAGCAGGCACTGA[C/T]TAACAGAGGCTGTGC | 114792 |
| rs188287937 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995658 | GCACTTCTCAGCTTT[G/T]CTAGTGACCATTCTT | 114792 |
| rs188294027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034530 | ATTTTAGCATTTTTT[C/T]TTCTATTTCTATAAA | 114792 |
| rs188297524 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059979 | TAAATGGTATTAGAC[C/T]ACTCTAATTTGCAGT | 114792 |
| rs188314927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995952 | GAAGTCCACCAAACT[A/G]CTGTTGAACACTATT | 114792 |
| rs188329585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915205 | TTAATCTCAATGGTA[A/C]CTACAGCTGTTTTGT | 114792 |
| rs188335500 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956686 | CAGTTTTACCTTAAG[C/G]ATTTCAGCTTGCTGA | 114792 |
| rs188343746 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982805 | TGGGGTTTTCTAGAT[A/T]TACAATCATGTCATC | 114792 |
| rs188349464 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933948 | AGTTTTCACTCTGTA[A/G]GGAGTGACCTTGACT | 114792 |
| rs188360426 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942770 | TAGAGAGATTGAAAA[A/G]GACTTTCCCCAGGTT | 114792 |
| rs188366808 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903597 | GCCCGATGTGACAGC[A/C]CACAAGAAACAGATA | 114792 |
| rs188367493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916017 | AATTAAAAGGAGTTT[A/G]ATTGAGTAATGAATG | 114792 |
| rs188371217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925237 | CCTTTCTTCCCTCCC[C/G]CTGAGCCCAATATGT | 114792 |
| rs188394123 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089550 | TTGGGAGGCTGAGGC[A/G]GGCAGATCACTTGAG | 114792 |
| rs188396536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126576 | AGAGTACACCACAAT[A/G]GCAATTGCACTGAAG | 114792 |
| rs188406692 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102878 | GGAGTACACGTGAAG[G/T]TTTCTTATATAGGTA | 114792 |
| rs188412557 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056307 | AGTCGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 114792 |
| rs188421717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026478 | GAAATGGTTGCTTAG[C/T]AACTAATGGGGTTAA | 114792 |
| rs188428866 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092707 | ATCTTTCCTTCTAAT[C/T]TATATGCGGCTAACT | 114792 |
| rs188430778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061430 | TTATTAAGACATTTT[A/G]TCTTGTCCACTGTTT | 114792 |
| rs188446875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020004 | CCAGGCTAGAGTGCA[A/G]CAATCTTGGCTCACT | 114792 |
| rs188460034 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984939 | GCTGGTTATTTTGCT[C/T]GTTAGTTGATGCAGT | 114792 |
| rs188464121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935298 | CTGCTCAATTCCTAT[C/T]GCAGGAAACTTTTTA | 114792 |
| rs188551118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117629 | ACAGGCTCCTGTAGC[A/G]TTTGACATTGTGACC | 114792 |
| rs188572599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041166 | TTGGCATTGCTGCAT[A/G]TAACTTGGTAGCAAT | 114792 |
| rs188582358 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082342 | GTTTAGGCTGGGAGC[A/G]GTGGCTCACACCTGT | 114792 |
| rs188589926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976493 | GGAGTGAGAGGATGC[C/T]TCTGGATTCAGGATC | 114792 |
| rs188590509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982179 | AGTATTATTATGTGG[C/T]TATTTAAGTCTCTTT | 114792 |
| rs188595701 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009531 | AATGTTTGGAAAGTT[G/T]TGTATGGACTGGAAA | 114792 |
| rs188601240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933311 | TACTTGGACCTCTTT[G/T]GGGAGATTTATATCC | 114792 |
| rs188626349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927427 | ATTAAATCCCAGCAC[C/G]CTGGTATACAAAATG | 114792 |
| rs188629871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090643 | CCAGGAAGAAGCAAG[A/G]AATTTAAATAGTACT | 114792 |
| rs188631762 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135471 | CCACCATGCCCAGCT[A/T]ATTTTTTGTATTTTT | 114792 |
| rs188663627 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069717 | AAGTAATTTTTCTCT[A/G]CTTTTTAAATATTAA | 114792 |
| rs188669916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097773 | CAAATGTTTCCATTC[C/T]GATTGTGCAGTGGGA | 114792 |
| rs188676814 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115296 | GTTGGGATTGCAGGC[A/G]TGAGCCACTGTGCCC | 114792 |
| rs188679546 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107074 | AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 114792 |
| rs188716639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999053 | GAGGCATCTAATAGG[C/T]AGATTAACAAGGCTG | 114792 |
| rs188771241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918819 | GAAATGTGTTTTGAA[A/G]CAGTAATGGGGCAGG | 114792 |
| rs188775339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094550 | AGTTATGCATTCTCC[A/G]TGGTGAGGATCCACC | 114792 |
| rs188810064 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035451 | TTTCTTATGCTTTCA[C/T]GTTACTGTTTAGCAT | 114792 |
| rs188814579 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075349 | TTACATATTTATATA[C/T]AAAATATGCCTATAT | 114792 |
| rs188816218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027337 | CTGGATGTGGCTTAC[A/G]GCCCTCAACGGGGCT | 114792 |
| rs188820077 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052883 | ATGGTATTATTAGAA[A/G]TATTATCAAGCAAAT | 114792 |
| rs188824369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996689 | CTTTTCCTCTCTTCA[A/G]CATTCTCAAGCAATA | 114792 |
| rs188828767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006937 | GTTTTTCTTTCATAT[C/T]TACCTTATGGAATCT | 114792 |
| rs188831097 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042356 | GTTATAACAGAAGCA[G/T]AATACAAAACAGAGT | 114792 |
| rs188840634 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983483 | CATATACCTCTGGTA[G/T]AATTCAGCTGTGAAT | 114792 |
| rs188842650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016897 | ATAAGAGGCCCTATC[C/T]CCTTCACTCTCTTCT | 114792 |
| rs188846218 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987785 | ACAGAACAGAGCCCT[C/G]AGAAATAATGCGGCA | 114792 |
| rs188856538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943732 | GCTTCCTTTTCCAGT[G/T]AAACACTTCGAGCTT | 114792 |
| rs188861057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970994 | GTTCACCAATAGACT[A/G]AATTGAGATAATTAT | 114792 |
| rs188867710 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925668 | TGTGTTTCCCCACAC[A/G]AGAATGAGCTTCTAT | 114792 |
| rs188875243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129965 | AAATAACCTTTCCCA[A/G]TTTGGCAAAAGATGT | 114792 |
| rs188880323 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989930 | TGTACTGTTTGTCAG[C/T]TCTATCAGATCAGTT | 114792 |
| rs188885971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946567 | TAGGAATTATTGTAA[C/T]TGTTTTGTGAGAAAT | 114792 |
| rs188898133 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907553 | ATTGCTAAACACTCT[A/T]TGTACAGGAAGCTCT | 114792 |
| rs188907563 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095035 | TTCATTTGCTCTTAA[A/T]ATAGCTTTTAATTTG | 114792 |
| rs188908902 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113670 | ATACTGTTTGTAAGA[A/C]AGTTTGTATTATTAC | 114792 |
| rs188920054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111651 | TTCTTTTATCTTTGC[C/T]ATCTGTGGATGGCTT | 114792 |
| rs188934186 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038454 | AGATGCAAATCAAAA[C/T]TACACTGAAATACCT | 114792 |
| rs188949019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079781 | AAAAATATTCCCTAA[A/G]GAACAACAATGTATG | 114792 |
| rs188988535 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938414 | GGGCCCCACAGTGGA[C/T]ACCTTCTCTTCTGGG | 114792 |
| rs189000406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947825 | AGAGGAATTAAGTAC[C/T]TGTCCAGAGTCACAC | 114792 |
| rs189005594 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900654 | CCTAGACTTTTACCA[C/T]TGGGTACTCCTTCTT | 114792 |
| rs189008851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108402 | CCACAAAGCTAACTG[C/T]TGTCTTTGGGTTTTA | 114792 |
| rs189009730 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922195 | GTCCCACACTACCAC[A/C]ACTGAGGGACAGGCC | 114792 |
| rs189042747 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069136 | CACATGTGGATCATC[A/G]AGTAAAGCAAAGCCC | 114792 |
| rs189060741 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031942 | GATTATAGCGACAGT[G/T]TCTATATAACATTTA | 114792 |
| rs189104959 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962816 | GAAAGGTAAGAAACT[A/C]CCCTAGCCTAGCTGC | 114792 |
| rs189113184 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919580 | GATTCCCACAATATT[G/T]AAGCAATTTTTTTTC | 114792 |
| rs189173489 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052623 | GTTGCCTGGCATCTA[A/G]CCTCCCAGCCACTGC | 114792 |
| rs189182758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096933 | TCTGCTAATGAAACA[A/G]CACTGAGAGGTTAGG | 114792 |
| rs189200945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134420 | ACAAACTTTTCTCTC[A/T]AAGAGTGCTTCTAGT | 114792 |
| rs189210324 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056403 | AGCCACCAGGCCCGG[A/C]CCACCAGCCTGCCTA | 114792 |
| rs189210607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944307 | AAAATATTTGTTCTT[A/G]TTTTATTCAGATATT | 114792 |
| rs189217193 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016385 | GATGTGAGACATGGC[A/G]TCAAAGGAGATCATT | 114792 |
| rs189239914 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905934 | AGTATATGAAGTGTC[C/G]TTGCTCATAGACTTT | 114792 |
| rs189281319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120490 | TCTGTTTTCAAATTT[C/T]TGTCGTTTTATGGTG | 114792 |
| rs189293460 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142220 | TGCACAAATAACTCA[C/T]AAATATGTATATAAA | 114792 |
| rs189299197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062022 | GAGATTTTCTGTGCT[A/G]AAGCATATTTTAGAA | 114792 |
| rs189300333 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124323 | TACTCCCAACTAGTA[A/C]CTTAATATCTCATTT | 114792 |
| rs189317876 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048634 | TGATAATGCAAACAC[C/T]GTGCATTACATTTTG | 114792 |
| rs189319570 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103492 | TGCTGGGATTACAGG[C/T]GCCCAGCCATGTATA | 114792 |
| rs189328714 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090007 | TAAACCCAAGTTATG[A/T]CCTATTTTAGTGTGG | 114792 |
| rs189356584 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012942 | CTCAGCACTCTAAGT[A/C]CAAAAGAGCCCTTTT | 114792 |
| rs189375104 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985659 | TTTCTTCCAGTTGAT[C/T]GAATCAGCTACTGAG | 114792 |
| rs189385197 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937196 | GAACATTTCTGTCAC[C/T]GCAAAATGTTCCCTC | 114792 |
| rs189408784 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900194 | AACACACTTTGCTCA[G/T]CTTAAAATTGGGATA | 114792 |
| rs189428067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107432 | AGTTTCTAGTTCTAG[C/T]TTTTCTGCTAATTCA | 114792 |
| rs189433732 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124053 | CCTGCAAATGAGTAA[C/T]ACTGCTAAAGAAATG | 114792 |
| rs189449892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067711 | TTAAATTCAGAACTA[A/G]GATGTTGATCTGGCT | 114792 |
| rs189450006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022556 | CTCACTGCAATCTCC[A/G]TCTCCCAGGTTCAAG | 114792 |
| rs189455896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048016 | ATATACACTATATGC[A/C]AAGCACTGTGATAAA | 114792 |
| rs189460088 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089705 | AGAATCAGTTGAAGC[C/G/T]AGAGGCAGAGGTTGC | 114792 |
| rs189464080 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007263 | GAGTTCTGAGACTCT[C/T]TCTTTGGCTTCATCA | 114792 |
| rs189469768 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039602 | TGAGGCAGGCGGATC[A/C]CAAGGTCAGGAGTTC | 114792 |
| rs189473867 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986221 | TGTTGCTGCCGGATC[A/G]TTCCTCTGGAATTTT | 114792 |
| rs189479152 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073786 | GCTATCCATGTGTCT[C/T]ATTTCCCTCCAGCTG | 114792 |
| rs189484229 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002502 | CTTTTAGGGTCAGGG[G/T]ACATGTGCAGGTTTG | 114792 |
| rs189484943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973087 | GATCCCTAACATATT[C/G]GTTCCAAAATATTTG | 114792 |
| rs189492138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965599 | TAATCAATATTCTTT[A/G]CAGTTTTAAAGCTCA | 114792 |
| rs189497360 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035096 | GATTATTTTTGTAGT[A/G]TTTGCCTTGATTCTT | 114792 |
| rs189502572 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939081 | TAAAGCTAGCAAACA[A/G]CTATGAGACATGGGC | 114792 |
| rs189517762 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926447 | TTCATATACTTCTTT[C/T]TTAATCCTCACAACA | 114792 |
| rs189523559 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116732 | AGACTCGCTAGATCC[A/G]TCGTCCTGGTATCAA | 114792 |
| rs189533859 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136960 | TGCGTCTTGAGCTCA[A/G]ATACTGGCTCCACCA | 114792 |
| rs189539504 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124704 | GGAGCTTTGCCCTCG[A/G]TTCCATTTCAGTTAG | 114792 |
| rs189555136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015153 | CCTAGCCATGTGCAA[C/T]TGTGAGTCAATTAAA | 114792 |
| rs189556979 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059235 | ACATATGGAAATTAA[A/G]GGAATGAGGAGGACA | 114792 |
| rs189561265 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081621 | CTCAGGGAAGCCTTT[A/G]CTAACTTTCCACTCC | 114792 |
| rs189562850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099752 | TTGATTCCTTACATG[C/T]TTGATTTCTGTTTTG | 114792 |
| rs189580141 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040536 | TGGGCCCTGCTTGGA[C/G]TATCAGTTTCAGTAA | 114792 |
| rs189580314 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953161 | GTGCAGCAGGCAAGA[A/C]GACCCCATCAGATGA | 114792 |
| rs189587074 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993576 | GGTGTACAAAAGGGC[A/G]TAGACACAAGTAGGG | 114792 |
| rs189591258 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024877 | ATGTATTTGTTTCAA[A/C]TATATATTGAAATAT | 114792 |
| rs189595566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932100 | AAAAAATACTGTTTT[G/T]TGATAGGCAGTGGTG | 114792 |
| rs189671281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120824 | TCCATGAAGAATTAA[A/G]TCTTTGTTGCTTTAG | 114792 |
| rs189728847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998036 | AATGGCAGCATAACA[C/T]TGACAGTAATTTTTG | 114792 |
| rs189729073 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959291 | GTGGTCTGCAGGCCC[A/G]GGACAGCTTCTGAGC | 114792 |
| rs189750159 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934658 | TAATTAGGCGGATTG[C/T]TGCAGAGAGCAGCTA | 114792 |
| rs189756621 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917463 | GACCTGAGGTCCATG[C/T]CCCAATCTGTTATCA | 114792 |
| rs189760346 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896551 | TATTTTAGAATTCTG[A/G]TAAATATCCAGTGAA | 114792 |
| rs189784907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006113 | CAGTGGAGTGTTTAA[A/G]CCTCTCATTATTATT | 114792 |
| rs189786861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970052 | CACCTCCATATGTAA[A/T]CTAACACCAAGACCT | 114792 |
| rs189787242 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934162 | ACTGTCCTGCAAATA[C/T]GTGCACTCTAGAGGT | 114792 |
| rs189804016 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109257 | GGAAAAAAATATAAA[C/T]CCAACAAGTAGGGAT | 114792 |
| rs189822069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080672 | CAAGTGTGGCTTGAA[C/T]GTACCTGGCATTGTT | 114792 |
| rs189824744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076099 | ATATAGAGCTTGAGA[A/T]CCAGAGTATATTATA | 114792 |
| rs189830853 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141359 | TATAATGTAATATTC[A/C]TTAATATTACAGAAC | 114792 |
| rs189841248 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035708 | CCACTGATGTCTTAT[A/G]GAGGTGGTTCCCTTA | 114792 |
| rs189849411 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061553 | TCAGATCTTGGGGAA[C/T]ATCTCTTCCTTCCTG | 114792 |
| rs189863000 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103236 | TTTTTTTTTTTGAGA[C/T]GGCGTCTCGCTCTGT | 114792 |
| rs189969365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129324 | AAATCCAAATTTTTC[A/T]TGGCAAAAAGGAATC | 114792 |
| rs189999141 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021744 | TAAAATTGTGAAATC[A/G]TATATCCAACAGCCT | 114792 |
| rs190003045 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057752 | TAATTTTAAAAAAGT[A/C]CAAGTTGTCAATTAT | 114792 |
| rs190018743 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987422 | GTGTCTTTGTTCTCG[C/T]TGGCAAACCACTGCT | 114792 |
| rs190029049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956911 | AGTAGCACATTAAGG[C/T]ATATAGTGATTTAAA | 114792 |
| rs190035346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916335 | ATTAAGTTAGGTCAC[A/T]GTTCATCCACAAGGG | 114792 |
| rs190036311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986130 | TTTGGAGTTTGTTGG[A/G]GGTCCACTCCAGACC | 114792 |
| rs190052373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138046 | AAAACACCAAATCCA[C/T]GGGAGGCAAATGTTT | 114792 |
| rs190073711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119485 | GGATATCAAGGTCCA[A/C]AATATTTCCACTGCA | 114792 |
| rs190083990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909003 | TGAAGGGTACAGAGA[C/T]CTGATAAAGGAAGAC | 114792 |
| rs190103540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017744 | TTGTATCTAGGTGGG[A/G]CCATATGACTAGCCC | 114792 |
| rs190115345 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053103 | ACACACACACACACA[C/T]GCACACACATTCTCT | 114792 |
| rs190154783 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112767 | ATTTTTTTAATTTTA[A/T]AAAAAAAAAGGAGAA | 114792 |
| rs190167437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132523 | GAGGCAGTGATTAGT[C/T]GCTGCAAAAATCCCA | 114792 |
| rs190183559 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077950 | ATAAGCTACATGCAT[G/T]AATAGCTTAGTGACA | 114792 |
| rs190186385 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056250 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 114792 |
| rs190189846 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904277 | AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 114792 |
| rs190195539 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929689 | TTCTTTTGTTCTTTC[A/C]CTATTTCGTATACAC | 114792 |
| rs190202729 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096291 | CTTGCAGGTAGACAC[A/G]CATGCACACACACAT | 114792 |
| rs190204543 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019317 | AGAGCCCTTGGACCC[A/G]ATAACTGCAGAAGGG | 114792 |
| rs190214754 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998650 | ATTTTACACTATCCT[A/G]CCCTGTGATTAATTA | 114792 |
| rs190218793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036325 | TCAATGATAATTTCT[C/T]AAAACAATAATTTTG | 114792 |
| rs190227382 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048827 | GATTTACTTATAAAT[A/G]TAACCCAATTGAGCT | 114792 |
| rs190231780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032553 | TTTAACCTTTGTTCT[A/C]AGGAAGTTTTTCCAT | 114792 |
| rs190244831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039215 | TAGCCATAAAAAAAT[G/T]AAATCCTGTCATTTG | 114792 |
| rs190276691 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964352 | ATGGTGAGAGAAACT[G/T]TTTATAAAAACAAAT | 114792 |
| rs190282600 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001790 | TCTAAGATAATGAAA[A/G]CAGATATTTTTAGAT | 114792 |
| rs190323150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928739 | AATTCATTTGGAGTG[A/G]GTAAATATATGGATT | 114792 |
| rs190365090 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093809 | CGATGGTGTAGTATA[A/G]AGCAGGAAATGAAAG | 114792 |
| rs190377188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128256 | GTATTTGGTATCTTT[C/T]TATTTTAGCAATTAC | 114792 |
| rs190410384 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926684 | GGGAGAGAGGGTAGG[A/G]AGTGGAGTGTGAACT | 114792 |
| rs190419104 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945083 | CTAGGTCTCTTGTTA[C/T]AAACTACTTAAAATA | 114792 |
| rs190421051 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906101 | CACACAATCCTCTGC[C/T]GAGTTTCATTTCTGT | 114792 |
| rs190422925 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916539 | TTCCTTTGCCTTGTC[A/G]CTTTCCCGTAATTTA | 114792 |
| rs190437584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910154 | CCACTACCTGCAACA[C/T]ACCCTATTTTGGAAT | 114792 |
| rs190447008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087618 | GGTAGGACAGGTAAT[A/G]GAAAACTGGATGGAG | 114792 |
| rs190466417 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044581 | TAAGAGAGATTGATA[G/T]TCTTTCTTCTTTAAA | 114792 |
| rs190466769 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115845 | AAATATTAAGAATAA[A/C]CCTGATGTTTGTACT | 114792 |
| rs190488195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062685 | GAATATTGAGCAACA[A/G]CTATGTGTGCTGAAC | 114792 |
| rs190496159 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081338 | ATGATGGGGACAGAG[A/G]ACTATTGCCTCCTGG | 114792 |
| rs190505437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028273 | TATTCCAGGGACCAC[A/G]CCTTAAGTAGGGAAG | 114792 |
| rs190509569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989205 | TGTATCAGTGGCCTA[C/T]ATACATAAGTGTTTT | 114792 |
| rs190509738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008263 | AACTCTCTGACAGTC[A/C]GGTGCAGTCTGCCAG | 114792 |
| rs190515677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945379 | TGTACCCTAAGACTG[A/G]GGCATGCCTGTGGGG | 114792 |
| rs190539725 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012248 | AGTGATGGACCTTGA[C/G]GTGGCAATACTATCC | 114792 |
| rs190564866 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978345 | TTCCCTTCTTTGCAT[C/G]CAAGTATTCTCCGTG | 114792 |
| rs190596101 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071508 | TTTCATGCATCTGGG[A/G]AGGGTTACTGACTCC | 114792 |
| rs190609199 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109923 | ATTACGTTTCAGAAA[G/T]TTTTCCCTGGTGCAT | 114792 |
| rs190611428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033315 | TTCACTTAGCATAAT[A/G]TCGTCCAAGTTCATC | 114792 |
| rs190619100 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110981 | AAGAACAGATAAGGA[A/G]CCATTTCAAACCACA | 114792 |
| rs190639973 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992536 | CCGGTTTTGAATTTC[A/G]TTTTGGGAAATGATT | 114792 |
| rs190641602 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003148 | TTTTCTCTGTAACCT[A/T]GCCAGCATCTGTTAT | 114792 |
| rs190641949 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967802 | ACAGGATAGATAGAG[C/T]AAGAAAATGCCTTCC | 114792 |
| rs190650230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979160 | TTAGGTCCCATTTGT[C/T]AATTTTTGGTTTTGT | 114792 |
| rs190656360 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013544 | CTCCCCACCACATAC[A/G]TACACAGACACACAC | 114792 |
| rs190666306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902186 | CCACAATGGTTGAAC[C/T]AATTTACACTCCCAC | 114792 |
| rs190668509 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923541 | GCACTACAAGCCAGA[C/G]AGATAACCTCCAGAG | 114792 |
| rs190679990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967478 | GTATATATATATAGA[G/T]AGAGAGATAGGGATA | 114792 |
| rs190684346 | snp | A/C/T | 0.00398691 | 0.0444912 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113335 | TCACATATTTTCTTA[A/C/T]GTTACTCATATTGAT | 114792 |
| rs190688439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133648 | CTAGCATATAGTTGT[C/T]GTGTTATCCTTAGTT | 114792 |
| rs190694046 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923215 | CAATCAATATAGATG[A/G]GCTTAAAATTTTAAG | 114792 |
| rs190722693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135585 | TTACAGGCGTGAGCC[A/C]CTGCATCTGGACGAT | 114792 |
| rs190742683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058591 | GCTCTTTTACAGCTA[C/T]GTGTAGCCACCCAGC | 114792 |
| rs190751217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099006 | ATCTTATAGGTTCGC[C/T]ATGTTTTTAAAGTAA | 114792 |
| rs190805742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031817 | ACTGTCATTTGGAAA[C/T]TATTTGAAATGAATG | 114792 |
| rs190831925 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948306 | CCTTGTACGTCAAAC[C/T]TGAGGTTGGTTCATA | 114792 |
| rs190853034 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092464 | TTTCTTTCTGAAACT[C/T]TTTATAGTTTCTCCC | 114792 |
| rs190874412 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050467 | GTGGGGCAGGGGCAA[A/G]GGCTACCCGCAGGTA | 114792 |
| rs190875934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018717 | TAATATGCTATAAAG[C/T]AGAATTCAAGATGAA | 114792 |
| rs190917553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986571 | CAAGCCTTGGCAATG[A/G]CGGGCGCCCCTCCCC | 114792 |
| rs190927917 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939895 | TCAAAGGTCATAGAA[A/G]TAGCTTAGCCTAGGG | 114792 |
| rs190951985 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901493 | ACATTGGACCTGCGT[G/T]GATAATCCAGGATAA | 114792 |
| rs190977288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106437 | ACAAGAAATAATCTA[G/T]AACTAAAATACATTT | 114792 |
| rs190982187 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122360 | TTAATGCATGGATTA[C/T]GTATGCTTCTATTCA | 114792 |
| rs191003008 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064012 | GGCATTACCTCTATG[C/T]GATGTCTTTGTATTC | 114792 |
| rs191007019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046052 | CAAACACCAGAGACT[G/T]ATTCTGACTGTGCAT | 114792 |
| rs191050198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912823 | ACTTCCATGATCCAG[A/T]TCCTCTGCATTGTAA | 114792 |
| rs191067079 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922780 | GCTCCTCTAGGAGTG[C/G]AGTAAACTGCAACAT | 114792 |
| rs191084758 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901007 | GAATACTGGGAGCGG[G/T]GGGTAGTGCCACAAA | 114792 |
| rs191086059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125827 | AGGCTGGGATATAGA[C/G]CACTATCTTCCTTGA | 114792 |
| rs191110094 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100710 | TGCTTGAGCCCTTGA[C/G]GTCCATTTGGTTATA | 114792 |
| rs191116449 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091739 | TTATTGTTAACTCTC[A/G]ATAGTTGTATGCACC | 114792 |
| rs191117489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041798 | TTTAATATGATCCAG[C/T]GAACATAGTATTTTA | 114792 |
| rs191119931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109793 | CTCTAGTGCTGTTTC[C/T]GGTAGTATCTATGTG | 114792 |
| rs191128008 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060154 | AAAAAATCTCCTTAT[A/G]CAAGAAATGAAGAAG | 114792 |
| rs191135976 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059850 | ATCCAGTTCATTTGA[C/T]GATTATAAATTCAAG | 114792 |
| rs191153351 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070735 | GATTTTAAAATCACT[A/T]TCAGTATGCATTTTT | 114792 |
| rs191178407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025223 | AAAATCTGATTTGGA[A/G]CGAATTGTCCATAGA | 114792 |
| rs191179034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913634 | ACTAGGTGAGCTTTA[C/T]TTTCATGAATAAGAA | 114792 |
| rs191206030 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126320 | AATATCTATTGGTGA[C/T]ATTTTCTTACTATGC | 114792 |
| rs191234114 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97041929 | AAGCTCGGTGACTCA[A/G]TCATGGCTTTATTGC | 114792 |
| rs191242236 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060875 | AATACAGCCACTGGT[C/T]GGTTCTTATCCCCAC | 114792 |
| rs191295698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043576 | TTCCTTTGGCTATTA[A/C]CCAGAAGTGGAATTG | 114792 |
| rs191307292 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086435 | TTAAAGAGCTGCAGC[A/G]TCCTGAAGGCCTTCT | 114792 |
| rs191309415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007779 | AGCACTCCTGGACTA[C/T]GTGCTCTAACTCTGG | 114792 |
| rs191325573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935259 | TATTGTGATGGCTTC[C/T]CTGATGTTGAGTTAG | 114792 |
| rs191348018 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898117 | AGTCACCCGGGAAGC[C/T]CTGTAAAGTTCTGTG | 114792 |
| rs191380365 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040773 | TTGGATCATGGGGGC[A/G]ATTTCCCCCATGCTG | 114792 |
| rs191384628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081960 | AGATCGCAGTGCCCC[A/G]GTCATGGAAGGCTAT | 114792 |
| rs191389454 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105315 | CATTCTATTAAAACA[C/T]GCTTTCCTGGCTTCC | 114792 |
| rs191401039 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003532 | TTGGTTTTGTTGCAA[C/T]TGCTTTCGGCATCTT | 114792 |
| rs191470839 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927392 | CAAAGGAATGAAAAC[A/G]TAAGTGGGAACTCAG | 114792 |
| rs191476942 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996985 | AAGTTTGAGGAATGG[G/T]TTGGGAGGTAGGTAA | 114792 |
| rs191491141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957910 | ACATCATGATTCAAT[A/G]TATGCAAATAATCTG | 114792 |
| rs191498795 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104525 | ATCTGTGATAAGCTG[A/T]ATATTGTTTTAAAAA | 114792 |
| rs191527518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062175 | ACACATGCTATGGAA[C/T]ATTCATCTTGTCTCT | 114792 |
| rs191561020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989031 | AATGGGTGCAGCACA[A/C]CAGCATGGCACATGT | 114792 |
| rs191564745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027990 | GGGTGATTGGAAGTC[A/C]ATATTTTGAAGGTTT | 114792 |
| rs191566978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960220 | TCCTTTTAACACGAC[A/C]CTGAGAAAGGCCTGC | 114792 |
| rs191575013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918240 | GGGTGAGTTAACAGA[A/G]CTCATAGGTAAAATA | 114792 |
| rs191579215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138909 | ATATACATGTATGTA[C/T]ATATGTACATCCAAA | 114792 |
| rs191580925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110253 | TTGGTATCTTATTTA[A/G]TTAAAAATGCTACCT | 114792 |
| rs191590597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986674 | GACCCTCCAAGCAAT[A/G]CACGGGATATAATCT | 114792 |
| rs191598841 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083118 | TGGGGAAGGCTGGGT[A/G]CCGTGGCTCATGCCT | 114792 |
| rs191602709 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035308 | TCTTTTTATATTGTG[C/T]ATCCATCAACAAATT | 114792 |
| rs191606571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071883 | TAATGCTAATCAACA[C/T]TGGACAATCTAAGTT | 114792 |
| rs191610821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950648 | TGAATGGTTAGTGAA[C/T]GACTAGTTACAGTAA | 114792 |
| rs191611609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052036 | CCTTTACTATCCTAA[A/C]ATGAAATTCCTAGAC | 114792 |
| rs191611745 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118359 | TGCAGTGGCTCACGC[C/T]AGTAATCCCAGCACT | 114792 |
| rs191618401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092711 | TTCCTTCTAATCTAT[A/G]TGCGGCTAACTCCTC | 114792 |
| rs191632766 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987606 | GGAAAAAACTACTTT[A/C]AAGTTCATATGGAAC | 114792 |
| rs191632962 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015540 | TTTGCCCCTGCCCTA[C/G]AGACCTGTGGAACTC | 114792 |
| rs191640316 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911799 | TGAAATATTCTTTTT[C/G]CATATATCTCCCTGC | 114792 |
| rs191646457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121436 | ATTGCTTAACTGTCC[A/G]TTCTTCTCAGGGGTG | 114792 |
| rs191646988 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970339 | GGCCTTACCTGCACC[A/G/T]TGTTCTCCTTTGTCC | 114792 |
| rs191648695 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034350 | GGATTTATTTCTGGG[A/G]TATTCTGTTTGTTGG | 114792 |
| rs191661334 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943173 | ATACATACACACACA[A/T]GCCTATACATACACA | 114792 |
| rs191668160 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994796 | AAGCAGTGTGAGCAC[A/C]GCATAGCATTAGCCA | 114792 |
| rs191669965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903779 | CCATTACTAAAAATA[C/T]ATTTAGCTAACAGGG | 114792 |
| rs191678815 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140110 | AAAAATTACTAGATA[A/G]AATTTGGAAACATGT | 114792 |
| rs191731105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983746 | CTTTATCATTTTCTG[C/T]TGCGTCTATTTCATT | 114792 |
| rs191746044 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906925 | GGCTTCCAGAGAAGT[C/G]TCCAGAGAAGGCTAA | 114792 |
| rs191782027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135034 | AACCACTGAGGATAT[C/T]TGAGAGTATCCTCAG | 114792 |
| rs191789766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990354 | GGGGGTGGGGGTTAT[A/G]TTAGCAAGTATTTTT | 114792 |
| rs191807787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080448 | CTCCCTACTGGATAC[C/T]AGGGACACACAAGGC | 114792 |
| rs191809903 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977600 | TTTCCCCCAGTAAAG[A/C]CTAAATGTTACAGAC | 114792 |
| rs191810964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097260 | GACTCCTCCATCACC[A/G]AGCTGTCACTCCAGC | 114792 |
| rs191817735 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114985 | CTATGCTGTGCATTG[A/C]GAGAAGGGATTTAAG | 114792 |
| rs191818065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927880 | GCAGCGTCCACTTTT[C/T]GAGCTCTTCTGTGAG | 114792 |
| rs191822835 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947483 | ATAAATCCCTCTCAA[A/G]GATTCTCATGAAAAG | 114792 |
| rs191825663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039141 | GGAATTAACTAAGTG[C/T]TCATCAGTGAATGAA | 114792 |
| rs191837822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908685 | AGTTAGAACTTAGAC[A/G]TCATCTAGGATAATC | 114792 |
| rs191842666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057092 | GTTAAAACTATTTTT[A/G]GAAATTAATACCCCA | 114792 |
| rs191854623 | snp | A/G/T | 0.00319074 | 0.0398324 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021394 | GGAAAGCTGGCAGGC[A/G/T]TGAGACCCAGAAAGG | 114792 |
| rs191883533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012029 | TTTGTAATCAATCAC[C/G]TAACTGCTGAATGCT | 114792 |
| rs191899547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047681 | GAAGAAGGAAGAGAA[A/G]TACTCTGATGGAAAT | 114792 |
| rs191902793 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029746 | AGTTAATTGAATGGT[C/T]TCATTAACTGAGATT | 114792 |
| rs191906491 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977909 | GAGTATCTGTAAAGT[G/T]GCCTTTTAGTTCCAT | 114792 |
| rs191906642 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963937 | TAGATGATCACAGTT[A/G]AAAGAGATCTCAAAG | 114792 |
| rs191910757 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130656 | ATGTTGATCTATTGA[G/T]TGATAAACATTAGGG | 114792 |
| rs191913538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990803 | GGAGCATTGGAGGCT[C/T]ATAGGTGAGCTAGAC | 114792 |
| rs191925822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930117 | ATACAAGATATTGAT[A/G]GAAAAAGAAGTCCCA | 114792 |
| rs191930344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028419 | TCTTCTGGTCTTAGA[A/G]AATTCTCCCTGAATT | 114792 |
| rs191939899 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096125 | TACCCCATCTCATCA[A/T]TCTCACACCCAACGT | 114792 |
| rs191959132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054832 | TACTCCCGGCTATTC[A/G]GGAGGTTGAGGTGGA | 114792 |
| rs191965258 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990163 | GAGAAAAAGACACTC[A/T]GGCTTTTTGACTTGC | 114792 |
| rs192020067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117640 | TAGCGTTTGACATTG[C/T]GACCCAATTCACAAG | 114792 |
| rs192021057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935444 | TGTCTGTGGAACTTC[A/G]GCAAATTAGATTTTG | 114792 |
| rs192039329 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898766 | TCCATTTCCTGAATG[G/T]GTTACTGTAGTGCTG | 114792 |
| rs192040569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082442 | CACGGTGAAACCCCG[G/T]TTCCACTAAAAATAC | 114792 |
| rs192043414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918930 | GAAGAGCCATCTCTC[C/T]GCCTGTGCAGTATAG | 114792 |
| rs192059327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050059 | ATGTGCTCAGAGTCT[A/G]GTTTGTGCTGCAAGA | 114792 |
| rs192075624 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014096 | CGGATCACGAGGTCA[A/G]GAGATCAAGACCACG | 114792 |
| rs192078743 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980190 | TCTGGCTAGGACTTC[C/T]AGTACTATGTTGAAT | 114792 |
| rs192090321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931231 | TTTTCTCTGCACCAC[A/G]ACCTCACTCATTCCC | 114792 |
| rs192174319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969031 | CTTCCTAACTGTAGT[C/T]GGGGTCATTGTCCTT | 114792 |
| rs192178092 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005562 | TCCTATTTCTTCTAG[A/G]TGTGATATTAGGTTG | 114792 |
| rs192199216 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96925017 | CCCAGCAGACCGCTC[A/C]CCCCATCGGGTAAGC | 114792 |
| rs192238169 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077370 | TAAAGGAAAATTAAT[A/G]TGAATTCATTTGATA | 114792 |
| rs192273549 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066350 | TTCTGTAAGTGAGAA[C/T]TCCAGATGAACATTA | 114792 |
| rs192281805 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009609 | TTTGTACATGCTTTG[A/T]TGTTGTTGTTACATA | 114792 |
| rs192286046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036114 | CTTGATCGAGTCTGG[C/T]ATTGAAGTTCTCTGT | 114792 |
| rs192289119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089592 | GAAACCAGCCTGCCC[A/G]ACATAGTGAAACCCC | 114792 |
| rs192294654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107109 | CATCTTGGCTAACAC[A/G]GTGAAACCCTGTCTC | 114792 |
| rs192328937 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946809 | TCTGGATTGGCTGAT[G/T]GTTTTATACTCTGGT | 114792 |
| rs192337184 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908357 | GTGTTCAAGAATAAA[C/T]GTATACTTGTAATGA | 114792 |
| rs192357724 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101116 | TTCAGCCAAGCTCAT[C/T]ATTCTTGAATCAATT | 114792 |
| rs192370687 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138296 | ATAATCCCAGCACTT[C/T]GGGAGGCTGAGGTGG | 114792 |
| rs192373181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108112 | TCTTACCTAATGGCC[A/G]TGTTTCCTAAGCACT | 114792 |
| rs192386797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124167 | TTATTTCAAAGGGGA[A/T]GGCAAGAGAACCAGT | 114792 |
| rs192405788 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032749 | ATGTAATAAAAAGCA[G/T]ACACTGAAAACAACT | 114792 |
| rs192419738 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089901 | ATTAAGACCAAAAAA[A/T]TTGCTGGCTATGTGA | 114792 |
| rs192454086 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993307 | GATTGGAGGCTAGTG[A/C]TCTAAGTTGGCCTTG | 114792 |
| rs192462321 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951744 | GATAAGTTTTATATA[A/T]TTTTTAAATTTAGCT | 114792 |
| rs192465718 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056570 | ACCCTCCTGTTTAAT[C/T]CAACTAGCTTCCTTG | 114792 |
| rs192470490 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038665 | TACTACTGAGTATAT[A/G]TTCAAAAGAAGGGAA | 114792 |
| rs192479229 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111034 | CAGAAAAGTCTTGGG[A/G/T]GGGGGGGGTCTTAGC | 114792 |
| rs192481130 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000792 | GCAACGAAGATGTTA[C/T]TCAGTAGGTGAATAG | 114792 |
| rs192492436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985590 | TTATTCTTTTTTCTC[C/T]AAACTTCTCTTCTTG | 114792 |
| rs192492482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020897 | CCAGGTTCAGTCCTT[C/T]CACCTTGCTGTCTCT | 114792 |
| rs192503409 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962419 | ATTTTTGCTGTGTTT[A/C]TGGGGGTTAATGCCC | 114792 |
| rs192512986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919480 | TCATATGTGTTTCAT[C/T]TGTTTGTTTTTGAAT | 114792 |
| rs192514226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936370 | GAAATGATTTGGCAC[A/G]TAGAACATAGTAGCA | 114792 |
| rs192522618 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074750 | ATAATGACTTCTATA[C/T]TATTCTTTTAAACAT | 114792 |
| rs192527405 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026236 | TGTGTTAGCCTGCAT[A/G]GACAAAGCATCAAAT | 114792 |
| rs192532758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110720 | AAAGGAAGTAAAGCA[C/T]GATAAAATTGAAGCA | 114792 |
| rs192536856 | snp | G/T | 3.30584e-05 | 0.00406548 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127502 | ATTATCTTAATTAAT[G/T]AATTTTAAAAGATTC | 114792 |
| rs192569515 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987351 | TGTGGGCATTTAGTG[G/T]TATAAATTTCCCTCT | 114792 |
| rs192572260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093448 | TCACAGTATAGATTT[C/T]AATGGAGGTCTCACT | 114792 |
| rs192576688 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942656 | GCTACAGCTGTGGGG[G/T]GTGTGTGTGTGTGTG | 114792 |
| rs192606037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025892 | TGACACAGGGCCTGC[C/T]ACATGGTAAAAGCTG | 114792 |
| rs192607982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933482 | CAACATTAAGTGAGC[C/T]CTTCACATCAGTGGC | 114792 |
| rs192609090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986972 | CATCGCTCACGCTGG[A/G]AGCTGTAGACTGGAG | 114792 |
| rs192610688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903409 | AATAGAATAGATTAC[A/G]GTCACTCTCATGATT | 114792 |
| rs192614482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004904 | TGGATTTTTGCATCT[A/G]TGTTCATCAAGGCTA | 114792 |
| rs192619202 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968088 | CTTCTTTCCATGACT[C/G]TGAAGCTATTAGAGG | 114792 |
| rs192623955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915620 | TTAATTTCTTGGCAA[A/C]TTCAATAAATTGATA | 114792 |
| rs192630487 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942506 | GTTGTTCTCTGGTTA[A/T]CTTATGTGTGTTTTC | 114792 |
| rs192636970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126714 | CTGGCTTTTGAAGAC[A/T]TAGTATGAAAAAAAG | 114792 |
| rs192638430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102887 | GTGAAGGTTTCTTAT[A/G]TAGGTAAACTGATGT | 114792 |
| rs192647397 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026815 | ATAATAAGTGATAAC[C/T]GAGGAAATTCCACAC | 114792 |
| rs192661090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061509 | TGTCAGGCCACTCAC[A/G]TTAGCTCCTATTCCC | 114792 |
| rs192703946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954107 | CTCCTGAATCACATG[C/T]CTTCCTTTTCTCAAT | 114792 |
| rs192718967 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900016 | AACACATTGAACAGC[C/T]AGTACACAGTAGGTA | 114792 |
| rs192721351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927506 | AGCTGCCATTTTCTC[A/G]TGTTTCTCCTAGAGC | 114792 |
| rs192724582 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122909 | CTGGCCACTGCAGGT[A/C]TCCAAGACAGTTGCA | 114792 |
| rs192734156 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088986 | TAGAAAAAGCCTATA[C/T]AGAAAAATATAACAT | 114792 |
| rs192748277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011113 | GCGTTTGGACATGAG[A/G]GAATTATCATGTATG | 114792 |
| rs192752423 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985758 | CTAGAATTGGTTATT[A/C]TAGTTAGCCATTCAT | 114792 |
| rs192753698 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046949 | AGTTGATTATATGTT[C/T]AGTCAGTTGTAATAT | 114792 |
| rs192792038 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093826 | GCAGGAAATGAAAGC[C/T]GATAAGGGAGGATCT | 114792 |
| rs192800877 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128301 | AATGAAGGCATTTCT[C/G]TCTTTGCAAAGTGTG | 114792 |
| rs192805039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052723 | CTGAGAAGGTAGTAT[G/T]GACTCGATTGAGAAG | 114792 |
| rs192815086 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078775 | ACACCTATTTTTAAG[A/G]TGACTGCATCCACTG | 114792 |
| rs192819907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999225 | ACATAGGGACACCCC[A/G]TCTCTACAAAAAATT | 114792 |
| rs192824949 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037489 | AACCAAAGAAGTAAA[A/G]TATCTATACAAGGAA | 114792 |
| rs192835094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929266 | CTATCAAGTACAATA[C/T]AAGCCAATATGATGA | 114792 |
| rs192852661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119086 | CTTCAATAATTATCT[C/T]GTCCTCTGGGAAACA | 114792 |
| rs192868913 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083950 | GTTTTGCTTAAGACT[C/T]ACAAAGCCCATCTGC | 114792 |
| rs192885457 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042162 | CTCAAATAAATCAAT[A/T]CAAATACAGACTGGA | 114792 |
| rs192896140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006515 | TGTTTACATTTAAGG[G/T]TAATATTGATATGTG | 114792 |
| rs192901588 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981780 | ATTTTTAAATAATTT[A/T]TTGACTTCTACCTTA | 114792 |
| rs192906193 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914495 | GCTTTACCAAATAGA[A/T]TATGCTTTGTCTACC | 114792 |
| rs192941712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065624 | AAAATTAATTTGAAG[A/G]AATAATAAATTCATC | 114792 |
| rs192948979 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106602 | ACAAAAAATAGCTGG[G/T]TGGTAATGGCGCACG | 114792 |
| rs192952849 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029481 | TATTTACAGTAATAT[A/G]ATTTTACTGTTTTAG | 114792 |
| rs192960820 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001295 | TGGAACTCTCTATAC[C/T]TTCTACTCAGTTTTA | 114792 |
| rs192968176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962843 | CTGCATATTGATATG[G/T]GCAAACAGCTTCATT | 114792 |
| rs193011898 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056320 | CCATGTTAGCCAGGA[C/T]GGTCTTGATCTCCTG | 114792 |
| rs193021453 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096623 | TTTTCCCCAGATATT[A/C]TTTTTGATATCCACA | 114792 |
| rs193032114 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948006 | TGCTCCTAAATGTTT[A/G]GTTTGGCTAGATGCC | 114792 |
| rs193035060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020031 | CACTGCAACCTCTGC[C/T]TCCTGGGTTCAAGCA | 114792 |
| rs193045464 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909204 | CCTTTGGTAGGGTTA[A/G]AGAATTCGGCATCCC | 114792 |
| rs193052493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097074 | TCTGCACTGTCAGAA[C/T]TCATAATAAGTCAAA | 114792 |
| rs193064544 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97134540 | GGGCAACAGTTCTCT[A/G]TAGTGCTGGAACACT | 114792 |
| rs193113810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052243 | GAATCACCATGATTG[A/G]GACAGCAGATGCACA | 114792 |
| rs193124393 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016037 | AGATTTAGAGGATGT[A/G]TGGAAATACCTGCAT | 114792 |
| rs193126532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982535 | TTAATTGGGGCATTT[A/G]GTTCATTTGCATTGG | 114792 |
| rs193141056 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902770 | GATTTCTGTGTATGG[G/T]GTAAGGAAGGGGTCC | 114792 |
| rs193156139 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933179 | CGCCTTTGAAAACAA[C/T]GACATATTTTACTCC | 114792 |
| rs193193955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123894 | GGTACTCCAGTCTAG[A/G]AGAAATTAAAACATA | 114792 |
| rs193232945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114693 | ATTGGAAATAATATG[C/G]CTTTCTGTGACTTTC | 114792 |
| rs193240570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080237 | TTGCCTTTGTGTGTA[C/T]GTGTCAGAAGGCCAG | 114792 |
| rs193251593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976571 | TATATGTATTGTTTC[A/G]GATATATATATATAT | 114792 |
| rs193257356 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141436 | TACAGCTATAGCCAA[G/T]AGTAGTACAAAAACA | 114792 |
| rs193270832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072874 | ATCTGTCTCCCCAAG[A/G]CATAAGTTTATGTCC | 114792 |
| rs193274207 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995828 | CCCCTTTTTTGAAAT[C/G]TTAATACTTTCAGCT | 114792 |
| rs193276513 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034648 | CATGGACATGGATGT[A/C]TTTCCATTTTATCTG | 114792 |
| rs193283950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955060 | AGAAACGAGAGAGGA[A/C]GCAAGCTCTGTTTTG | 114792 |
| rs193287890 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924332 | GGTTCCCGGGTCTCA[C/G]TCGCCGCAGTGGTGG | 114792 |
| rs199501875 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069418 | TTTTTTTTTTTTTTT[A/C]TACCAATGGCAATTT | 114792 |
| rs199528906 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057178 | TGTGAGTATCTTTTT[G/T]TTTTTTTTTTTTTTT | 114792 |
| rs199535871 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039849 | CAAACAAACAAAAAA[A/C]AAAGAAAGAAAAGAA | 114792 |
| rs199539877 | snp | G/T | 0.00021563 | 0.0103812 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114529 | AACATACCTCATGTT[G/T]GATTTATCAAAACAC | 114792 |
| rs199552121 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057173 | TCCTATGTGAGTATC[-/TTTTTTTTTTTTTTTTT]TTTTTTTTTTTTGAG | 114792 |
| rs199571265 | in-del | -/AAAAAAAAA | | | intron-variant, cds-indel, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010127 | AGGCACTGATTTGAC[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 114792 |
| rs199571545 | in-del | -/TCTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091972 | GCCCTTCTTCAATTC[-/TCTT]TCTTTCTTTTTTTTT | 114792 |
| rs199603094 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924830 | ACACACACACACACA[A/G]ACACACTTTCGCACA | 114792 |
| rs199639134 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931113 | CACCAGGATAAAAAA[A/C]AAACAAACAAACAAA | 114792 |
| rs199647321 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100799 | TCTTGGCTCATTATT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs199665711 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042624 | TCACCTACCTACCTA[-/T]TTTTTTTTGTGGTGA | 114792 |
| rs199671024 | in-del | -/GCA | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938630 | CCTTTCTCTCTTCCT[-/GCA]GCAGCAGCAGCAGCA | 114792 |
| rs199694130 | in-del | -/AGAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023216 | ATTTAGAAATTGTAA[-/AGAC]AAAAAAGCCACAATT | 114792 |
| rs199719057 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043451 | TACATACCATCTTTT[A/C]TTTATTCATCTGATG | 114792 |
| rs199719221 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984912 | GAATTTGATCCTGTC[A/G]TTATGATCTTAGCTG | 114792 |
| rs199719549 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029491 | AATATAATTTTACTG[G/T]TTTAGTTTGTCTTGT | 114792 |
| rs199727367 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112795 | GAATTTCTTAAAACT[A/G]AAGCAGGTACATTAT | 114792 |
| rs199732174 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922044 | TCTTTAATATACCAA[C/T]GTGACATGAACCTAG | 114792 |
| rs199732726 | snp | A/C | 0.255224 | 0.249945 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988622 | TATACCCAAAGGATT[A/C]TAAATCATGCTGCTA | 114792 |
| rs199748357 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956171 | CACGAGAACAGCATG[A/G]GAAAGACCTGCCCCC | 114792 |
| rs199766441 | in-del | -/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943139 | GCATATAGACACATA[-/TG]CACACACATATATAC | 114792 |
| rs199773928 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069585 | ACCTCCAGTTACACT[-/T]GTGGGGCTTTCGAGC | 114792 |
| rs199782589 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901342 | CCTTTTTTTTTTTTT[A/T]ACTTTAAATGGGGAA | 114792 |
| rs199822043 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031944 | TATAGCGACAGTTTC[-/TA]TATATAACATTTACT | 114792 |
| rs199840742 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133838 | TCTGAATGGATATGG[G/T]TTCTGACTGAGCAGT | 114792 |
| rs199848046 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138251 | TGTGCTATATAAGAA[A/G]AGAGAGGCCAGGCAC | 114792 |
| rs199850345 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117839 | ATGAAGAACAGCTTA[-/T]TTTTTTTCATTTTCA | 114792 |
| rs199857785 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040868 | CTCGGCACTTCTCCT[A/T]TCTGCTGCCTTGTGA | 114792 |
| rs199860998 | in-del | -/TTTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053801 | TTGTGTACTATGCCT[-/TTTA]TTTATATACTATGCA | 114792 |
| rs199865563 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987196 | TTGAAGGGTTTTTTG[A/G/T]GTCTCTATTTCCTTC | 114792 |
| rs199871940 | in-del | -/TATT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043457 | CATCTTTTCTTTATT[-/TATT]CATCTGATGATGGAC | 114792 |
| rs199889895 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115992 | GACAGCAGAAGAACA[A/G]TCAAAGTCCAAATGA | 114792 |
| rs199890074 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967464 | ATATAGAGAGATGTG[-/TA]TATATATATAGAGAG | 114792 |
| rs199928383 | in-del | -/GAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964174 | TTTCTGGATTCTGAG[-/GAG]GGGAACTGCAGGAGA | 114792 |
| rs199933247 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057692 | CTTAGCCTATGGCTT[A/C]TCTTCTCAATTTCCT | 114792 |
| rs199936224 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027178 | AAAAAAAAAAAAAAA[C/T]AAAAAGAAAAGGGAT | 114792 |
| rs199937510 | in-del | -/T | 0.209997 | 0.246779 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022471 | TGTGATAACACCTAA[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs199967868 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069401 | GGGTGATTTTGTTCC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs199991035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137410 | AAAGAGATTGGGACA[G/T]CTAATCTCCACTTGT | 114792 |
| rs199993341 | in-del | -/TGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932241 | TTCAAAGCCTAAAGA[-/TGT]AATATGGAATCAATG | 114792 |
| rs199994944 | in-del | -/TATA | 0.0135371 | 0.0811498 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142186 | ATATACTTTTATTAT[-/TATA]TATAATTTTATCATA | 114792 |
| rs200024673 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089796 | AAAAAAAAAAAAAAA[C/T]AACAGTACTTTTCTT | 114792 |
| rs200032019 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111035 | GAAAAGTCTTGGGGG[-/T]GGGGGGGTCTTAGCC | 114792 |
| rs200042045 | in-del | -/AGATCCC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925568 | AGATGACTGCAGTTT[-/AGATCCC]TTCTTCCCCTCTATT | 114792 |
| rs200056339 | in-del | -/A | 0.0142736 | 0.0832652 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897859 | ACACCGGCGCAGGAC[-/A]AACTCCGGGACACCC | 114792 |
| rs200063242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966670 | GGTTTAGATCATTGT[A/G]TCTTTATTTTATCCA | 114792 |
| rs200104020 | snp | A/G | 1.64996e-05 | 0.0028722 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064683 | CGGGCAGTCACCTAC[A/G]GCTGTTGGAGCTTCT | 114792 |
| rs200128085 | snp | C/T | 1.65935e-05 | 0.00288036 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139269 | TGCCTCATCACAGGA[C/T]TGGCACCATCTGAAA | 114792 |
| rs200133740 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983274 | ATGTGCTGCTGGATT[A/T]GGATTGCCAGTATTT | 114792 |
| rs200134981 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994754 | AATAATGCTTTAAAA[-/G]AATAACAAAAATGTT | 114792 |
| rs200171080 | in-del | -/AC | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140232 | AACTTGCCTCAAGTA[-/AC]TCTCAGATGTCTTAT | 114792 |
| rs200214937 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082912 | CACATGCTTCATTTT[C/G]ACCTCTTTGCATCAG | 114792 |
| rs200218799 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003368 | TTTGCTTGTTAATTT[A/G]AGTTCCCTATAGATT | 114792 |
| rs200229771 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139434 | CAATTTTCTAAAATA[C/T]GTTATTGAAAACTCG | 114792 |
| rs200233154 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097644 | CTGCCTTTTTTTTTT[C/T]TTTTTTCAAATGGAG | 114792 |
| rs200244221 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988095 | AACAAAAGCCAAAAT[A/T]GACAAATGGGATCTA | 114792 |
| rs200290327 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082625 | CTCAAAAAAAAAAAA[-/A]TAAATAAATAAAAAG | 114792 |
| rs200306891 | in-del | -/T | 0.373799 | 0.217195 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941749 | GTGTCACATAGCTGC[-/T]CTTTTTTCTCTGATT | 114792 |
| rs200308940 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911850 | TTTTTTTTTTTTTTT[G/T]TGGCAGCTGCCACTC | 114792 |
| rs200313479 | in-del | -/A | 0.130694 | 0.219696 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997584 | AGACCCTGTCTCTAT[-/A]AAAAAAAAATTAGCT | 114792 |
| rs200316210 | in-del | -/TGTCTCTCTG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062184 | ATGGAATATTCATCT[-/TGTCTCTCTG]TGATCACTGTCTTTG | 114792 |
| rs200341584 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916365 | CTCAAATATAGAAGT[-/AC]ACAGTCTTTCTCAGG | 114792 |
| rs200346147 | in-del | -/T | 0.0182019 | 0.0936463 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043977 | CGAGTTCTCAGTTGT[-/T]ATTTTTTTTTTCTTG | 114792 |
| rs200346255 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943070 | CACACACACACACAC[-/AC]TCTGTACATACACAC | 114792 |
| rs200358952 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984521 | AGTCTAAGTCTCTTT[A/G]TAGGTCTCTAAGGAC | 114792 |
| rs200370685 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113818 | ACACAACTGCCACTA[C/T]CAGTACATGGACGAG | 114792 |
| rs200381825 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074616 | TTTAAAAAAAAAAAA[A/C]AAAAAAACTACTTTA | 114792 |
| rs200402871 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068013 | AACTTCATACAGACA[C/G]ACACACACACACACA | 114792 |
| rs200410614 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982690 | TCTGTTTGTCTGTTA[C/T]TGGTGCATAAGAATG | 114792 |
| rs200415274 | snp | A/C | 3.30896e-05 | 0.00406739 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139259 | ACTCTTCAAGTGCCT[A/C]ATCACAGGATTGGCA | 114792 |
| rs200419793 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915664 | GGAGTAAAAAAAAAA[C/T]GGGATGGATAATACT | 114792 |
| rs200421818 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904920 | GCTTTTTCCCCTTGC[-/T]CTCCATTCCCATTTA | 114792 |
| rs200463821 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027576 | CAAAATAATTGGGGG[A/G]AAAGGGAGACAGTGT | 114792 |
| rs200484158 | in-del | -/CCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97008045 | CAGGGCAGTGGCATT[-/CCT]GCTGCACCTCCTCAT | 114792 |
| rs200499204 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981433 | TTGCATTTATTTGGA[-/T]TTTTCTGTCTTTCTT | 114792 |
| rs200511597 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029494 | ATAATTTTACTGTTT[C/T]AGTTTGTCTTGTGAT | 114792 |
| rs200518424 | in-del | -/AGTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949330 | TCTGATATTCTAGTT[-/AGTC]AGTTTTCTCTTCATG | 114792 |
| rs200535364 | in-del | -/GG/GGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018153 | TTAATATTGAATCGA[-/GG/GGA]AACTTTTTTCAATGC | 114792 |
| rs200539020 | in-del | -/AA | 0.0425829 | 0.139564 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958098 | TCCAAACTGGGAAAC[-/AA]AAGAGAACAAATGGG | 114792 |
| rs200555785 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132888 | AACTAGTTCAGCCAC[-/T]AAACTTCATCCTGTA | 114792 |
| rs200562361 | in-del | -/GTT | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981355 | ACATAGAGGTTTGTA[-/GTT]GTCTTTGAGGTTTTT | 114792 |
| rs200570318 | in-del | -/AT/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103775 | TTATAGACAAAAAAA[-/AT/T]TGTCACCTTGTTTTT | 114792 |
| rs200576405 | in-del | -/AGT | 0.0107289 | 0.0724523 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946950 | TATATACTTATTAAC[-/AGT]GGGCACATATTTAAT | 114792 |
| rs200610964 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123715 | GTGGGGGAGGGAGAT[G/T]AAAACTGCCAATCTA | 114792 |
| rs200624333 | in-del | -/CT | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963642 | GAGGCAAATCCCTTC[-/CT]CCTTCCCGGGTTCAT | 114792 |
| rs200679972 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953788 | ACAATCTAAATGTTA[A/T]TTATATAATCAAACC | 114792 |
| rs200707610 | in-del | -/TTTCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091978 | CTTCAATTCTCTTTC[-/TTTCT]TTTTTTTTTTTTTTT | 114792 |
| rs200708338 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116251 | ATATGTAGATATATT[-/T]AAATTAAAACCTCAT | 114792 |
| rs200710485 | snp | C/T | 0.0039921 | 0.0444985 | intron-variant, missense, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105506 | CCTGGCTTACCTCAA[C/T]GGGATGACAAGACTG | 114792 |
| rs200716195 | snp | C/T | 0.000165319 | 0.00909023 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132645 | TTATTCAATTCTCTT[C/T]ACTTTAGGCCAAAAT | 114792 |
| rs200721881 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903121 | CAGAAAACAAACAAC[-/A]AAAAAAAACAGTTGG | 114792 |
| rs200738270 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074603 | TTTAAAAAAAAAAAA[-/A]CAAAAAAACTACTTT | 114792 |
| rs200765855 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057552 | CAGATCTTTTACACC[C/G]CCCTCCCGCCCCCAT | 114792 |
| rs200772875 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073737 | GTATTTATTTAAAAG[-/A]AAAAAAATCTGAATT | 114792 |
| rs200785174 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070828 | AACAAACAAACATCA[A/G]TCTCACTGAGTTCCA | 114792 |
| rs200790057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987932 | TGGATCCCTTCCTTA[C/T]ACCTTATACAAAAAT | 114792 |
| rs200791617 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043458 | CATCTTTTCTTTATT[A/G]ATCTGATGATGGACA | 114792 |
| rs200832438 | in-del | -/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018601 | GCAAGACTCAGTCTC[-/AA]AAAAAAAAAAAAATC | 114792 |
| rs200839376 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017688 | TTGGGGATATGGCTT[A/C]GAAATTCTTCTCAGC | 114792 |
| rs200860900 | snp | A/G | 3.30464e-05 | 0.00406474 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114515 | TGGATATCAGGTAGA[A/G]CATACCTCATGTTGG | 114792 |
| rs200881659 | in-del | -/TTATT | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938746 | TCTTGGGAAAGTTAC[-/TTATT]TTATTTCTTTGAACC | 114792 |
| rs200882759 | in-del | -/G | 0.0123036 | 0.0774623 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897893 | CATGCGCACAAGTGA[-/G]GGGGAAGCCCCGCCG | 114792 |
| rs200908228 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983277 | TGCTGCTGGATTTGG[A/T]TTGCCAGTATTTTAT | 114792 |
| rs200919322 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987973 | TGGATGAAAGACTTA[A/C]ATGTTAGACCTAAAA | 114792 |
| rs200996198 | snp | A/G | 7.19243e-05 | 0.00599641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085388 | CTGAAAAAGCATGCC[A/G]TGATTGGAAGTTAAA | 114792 |
| rs200996898 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901893 | CTCCAGCTCCATCCA[A/T]GTCCCTGCAAAGGAC | 114792 |
| rs201026359 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044908 | CTTCTCGTTTTTTTT[-/C]TTAGTCTGGCTAAAG | 114792 |
| rs201027681 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068178 | ACCTTTCCAAAAAAG[-/A]AAAAAAAAAAGTTTA | 114792 |
| rs201035836 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987205 | TTTTTGAGTCTCTAT[C/T]TCCTTCAGTTCTGCT | 114792 |
| rs201058077 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039846 | AAACAAACAAACAAA[A/C]AACAAAGAAAGAAAA | 114792 |
| rs201072661 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037394 | GTATAGACTTGTGAG[G/T]ATAAAAAAATAACAT | 114792 |
| rs201090565 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917533 | AACAACAGCTATGAC[A/G]GAGGCACCATTTCTT | 114792 |
| rs201100884 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072898 | TATGTCCCAAAGTTG[C/T]GTGATGTCGGACAAG | 114792 |
| rs201146068 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003392 | ATAGATTCTGGATAG[C/T]AGACCTTTGTTGGAT | 114792 |
| rs201152277 | snp | A/G | 0.0534909 | 0.154545 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114211 | CCTGTTTGTGGCAGG[A/G]GGGGAAGTTGAGCAT | 114792 |
| rs201176127 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068010 | GAAAACTTCATACAG[-/AC]ACACACACACACACA | 114792 |
| rs201179502 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047514 | CCTTAGAGAGAAAAG[A/G]ACAAAGTGAATCTAA | 114792 |
| rs201254901 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099889 | TAAAAAAAAAAAAAA[-/A]TCTGTGATCATTGTG | 114792 |
| rs201266476 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024414 | GCTTTTTTTTTTTTT[-/T]CAAATTAAATGACTT | 114792 |
| rs201267899 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057172 | TTCCTATGTGAGTAT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs201280180 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931110 | GCTCACCAGGATAAA[A/T]AACAAACAAACAAAC | 114792 |
| rs201338952 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973742 | TGCCTTTTTTTTTTT[A/T]GACAGAGTCTCGCTC | 114792 |
| rs201348997 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980003 | ACTGATATTCGTACA[A/T]TTGATTTTGTATCCT | 114792 |
| rs201366219 | in-del | -/GG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942651 | ACTTGCTACAGCTGT[-/GG]GGGGTGTGTGTGTGT | 114792 |
| rs201390123 | in-del | -/TGTG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942691 | GTGTGTGTGTGTGTG[-/TGTG]ATTCAGAATATCCCT | 114792 |
| rs201401206 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087105 | TTTAAAAGCTGCTTT[-/C]TGCTGCAGGCAATAA | 114792 |
| rs201441397 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988489 | GGAGAAATGGGAACA[C/G]TTTTACACTGTTGGT | 114792 |
| rs201450529 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946180 | TTATTTAGGAAAAAA[-/AT]ATTTTAAATATTTTG | 114792 |
| rs201452057 | in-del | -/CTCCTAATC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993721 | GTAGAAGACATAAGA[-/CTCCTAATC]AGAAACAAAGGAGTT | 114792 |
| rs201461937 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004313 | ATGCTACTGATTTTT[A/G/T]TACACTGATTTTGTA | 114792 |
| rs201495784 | snp | C/G | 8.41078e-05 | 0.00648435 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897629 | CAGCACAGGGACTCC[C/G]CGCCCCCGGGCCCCG | 114792 |
| rs201507523 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101923 | TGAATTTAAAAGGAT[A/C]ATTATATTGGGGAAT | 114792 |
| rs201606312 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037407 | AGGATAAAAAAATAA[-/C]ATTTGTTAAAATAAA | 114792 |
| rs201619008 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984523 | TCTAAGTCTCTTTAT[A/T]GGTCTCTAAGGACTT | 114792 |
| rs201619698 | in-del | -/T | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092453 | CACTTCTTAATTTTC[-/T]TTCTGAAACTTTTTA | 114792 |
| rs201684071 | in-del | -/TGA | 0.0520825 | 0.152737 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018150 | TAATTAATATTGAAT[-/TGA]CGAAACTTTTTTCAA | 114792 |
| rs201711368 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115994 | TTTGGACTTTGACTG[-/T]TTCTTCTGCTGTCCT | 114792 |
| rs201740230 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932222 | TTTTTTTTTTTTTTT[G/T]AGATTTCAAAGCCTA | 114792 |
| rs201750685 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922506 | AAAGACTCACACTTT[A/T]AAAAAAAAAAATCTT | 114792 |
| rs201751081 | snp | C/T | 3.36118e-05 | 0.00409936 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139298 | AAAGCCAAGCCATCA[C/T]GAACAGGAGGAAAAC | 114792 |
| rs201765520 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140236 | TGCCTCAAGTAACTC[A/T]CAGATGTCTTATTTA | 114792 |
| rs201771990 | snp | A/C | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010136 | TTTGACAAAAAAAAA[A/C]AAAAAAAAAAAAAAA | 114792 |
| rs201778895 | snp | A/G | 3.29919e-05 | 0.00406138 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114241 | TGCCAGTGGCCGGAC[A/G]TGTGCTGTGAGGACT | 114792 |
| rs201783265 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911824 | CCCTGCTCGGTCCTT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs201790225 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987948 | ACCTTATACAAAAAT[C/T]AATTCAAGATGGATG | 114792 |
| rs201814348 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031948 | GCGACAGTTTCTATA[-/T]TAACATTTACTATGT | 114792 |
| rs201822634 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112762 | GATGAATTTTTTTAA[-/T]TTTAAAAAAAAAAAG | 114792 |
| rs201828061 | snp | A/G | 0.000132507 | 0.00813856 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130773 | ATAAGTGGATAAGCC[A/G]TAGCCCCATGCTGCA | 114792 |
| rs201860397 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037405 | TGAGGATAAAAAAAT[A/T]ACATTTGTTAAAATA | 114792 |
| rs201917814 | in-del | -/ATATGATTAA | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106237 | ATATTTCTGAAATAC[-/ATATGATTAA]ATTGCATATTTTAAT | 114792 |
| rs201949924 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136068 | AATTTTTTGTGTCGT[A/C]AGTCACAAATCTGTA | 114792 |
| rs202015191 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953329 | TTTCCCATGAAAAAA[-/G]ATGAAAATTTAGGTT | 114792 |
| rs202020856 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093164 | GTAATATTGCTGCTA[G/T]CCTGGGTTATCAGGG | 114792 |
| rs202022592 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999067 | GCAGATTAACAAGGC[C/T]GTGGGGAAGTGATAC | 114792 |
| rs202031532 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118660 | CAAAATATTGGGAAC[A/T]AACAGCAGGCATAGC | 114792 |
| rs202075220 | in-del | -/A | 0.0217236 | 0.101931 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106460 | ATACATTTAAAAAAT[-/A]GACCGGGTGCAGTGG | 114792 |
| rs202093124 | snp | A/G | 1.6486e-05 | 0.00287102 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085266 | AGAAGAAGTTCTAAC[A/G]CTTCCCTATTGCCTG | 114792 |
| rs202110375 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124310 | GGACTTTAATTTTTA[C/T]TCCCAACTAGTAACT | 114792 |
| rs202142656 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987975 | GATGAAAGACTTACA[C/T]GTTAGACCTAAAACC | 114792 |
| rs202154686 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038337 | AGCAAAAAAAAAAAA[-/A]TCCAATTTAAAAATG | 114792 |
| rs202164074 | in-del | -/GCA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97008051 | AGTGGCATTCCTGCT[-/GCA]CCTCCTCATGCAGGT | 114792 |
| rs202168866 | in-del | -/GG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138257 | ATATAAGAAGAGAGA[-/GG]CCAGGCACAGTGGCT | 114792 |
| rs202220717 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946174 | ATGAGTTTATTTAGG[-/A]AAAAAATATTTTAAA | 114792 |
| rs202227633 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073347 | CACAAATAATTAAAT[A/G]AACCGTCACTTTCTT | 114792 |
| rs202232259 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950244 | TTAAAAAAAAAAACC[A/C]TTAGCTCTCTAAACA | 114792 |
| rs202243459 | in-del | -/A | 0.00835141 | 0.0640778 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900383 | GTGAATGAAAGTGAT[-/A]AAAAAAATTTGAGAT | 114792 |
| rs207467284 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901960 | ATGGTGTATATGTAC[C/T]ACATTTTATCCAGTC | 114792 |
| rs207467285 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936587 | TATGTCACAACTTCC[A/C]ACTACCATTCTTGTC | 114792 |
| rs267601172 | snp | A/G | | | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114158 | GCTCCCATGCCTGTG[A/G]GAAGGAGCCACCATT | 114792 |
| rs367545119 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131757 | GCTGGGGGAGGCAAC[A/G]CTGGGAATCTAATCA | 114792 |
| rs367545227 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986793 | TCTTTGACTAGGAAT[G/T]GGAATTCCCTGACCC | 114792 |
| rs367556900 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924025 | ATTGCTGAATTAGTA[C/G]TAACCACAGTAATCA | 114792 |
| rs367556938 | snp | A/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132712 | TTAGTTGGTGGATAT[A/T]CAATTTGGACAAATG | 114792 |
| rs367558049 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917134 | CAAGATTCTTATGTT[A/G]GAAATTATAAAACCC | 114792 |
| rs367637324 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035657 | ATGTGTCGTCCCACT[C/G]TCTTCTGGCCTGCAA | 114792 |
| rs367645052 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055140 | CTAGTAAATTTGCTT[C/T]CCTCCTCTTCTTGAT | 114792 |
| rs367684690 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101269 | ATAGAAAGATGATTC[C/G]TGTGCGTTTCTGAAA | 114792 |
| rs367731182 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965552 | AAAACACTGGACTTT[C/T]AGAAAGATTAAGGTG | 114792 |
| rs367739784 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971163 | ACTTAAAAACTACTG[C/T]ATATTTTTTATATAT | 114792 |
| rs367755909 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990828 | CTAGACTGGCCTCTT[A/C]TCTTTAAGATGGCTG | 114792 |
| rs367784018 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111110 | CAGCAACACTGAGGA[A/G]TGGCCTTGGCCAGAT | 114792 |
| rs367788992 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898405 | CCTTTCGATGAGTAT[C/T]TGTTCTCAGCCGCTC | 114792 |
| rs367803661 | in-del | -/AAAAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903882 | CTCACAAAGAACAAG[-/AAAAG]GAAATAAGAATTATA | 114792 |
| rs367825011 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126657 | TATTGAATCCTTGAA[C/G]CATGGCTAATCTGTA | 114792 |
| rs367829305 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042684 | GTTGAACTATACAAT[A/G]CATTATTATTTATTA | 114792 |
| rs367834548 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942250 | CCAGACTGGTGCTGC[C/T]CCTGTACTACTGCTG | 114792 |
| rs367843263 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927025 | TTTTATTTCAATATT[A/G]AAGTCTAATAAATGC | 114792 |
| rs367848654 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024461 | AACTGAGCACATTTC[A/G]TTAAAAATGGATTTC | 114792 |
| rs367860884 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984819 | GATGGGTCTTGACTC[-/TT]TATCCAATTTGCCAG | 114792 |
| rs367864620 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036691 | TTGTGTGACACTGTC[A/G]TGGTGCATGGGGGTG | 114792 |
| rs367898324 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102409 | TTTATTGACCAAATT[A/G]GTTTTCTCTCATTTT | 114792 |
| rs367920239 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103213 | AAACTTGAATTTATC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs367944225 | in-del | -/GAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083977 | CTGCCCCAAAAGGAG[-/GAG]TGTGTGCTATGTTGT | 114792 |
| rs367946136 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111406 | GCGGGAACTGGAATG[C/T]GGGTGCTGGGGCTAG | 114792 |
| rs367957659 | snp | C/T | 8.24804e-05 | 0.00642132 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127475 | CAGGTAAGAATCATG[C/T]AAGAACACCTCATTA | 114792 |
| rs367974948 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945714 | GAAATGGCATTCTTG[A/G]GCAGTGTCTTCTTCA | 114792 |
| rs367975087 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009485 | CTTCTGTTTTAATTT[G/T]CAATAGAGCACTTGT | 114792 |
| rs367979395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997515 | CCCTTTGGAAGGCCC[A/G]ATGGGGAGAATTGCC | 114792 |
| rs367990149 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963528 | TGCTGGTTCTCAATG[A/G]CTTTTAGGTCAAAAT | 114792 |
| rs367991617 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105120 | TGTAATATTAAAAGG[-/AT]AACATGCTAAAGTTT | 114792 |
| rs367993203 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002102 | GTATGCTTCTAGTCC[A/G]AGTCTGAAGGCCTGA | 114792 |
| rs367993663 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969926 | TCCCAAACCAAATTC[A/C]TCATCATTCTCTTCT | 114792 |
| rs368001833 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985630 | ATTCATTTCATCTTC[C/T]ATCACTGATACCCTT | 114792 |
| rs368004464 | snp | C/T | 1.66582e-05 | 0.00288597 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967065 | CCAGCTGGAAAATGC[C/T]GTCTGAACGCTGCCT | 114792 |
| rs368022122 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098708 | TTATTTAAAAAATAA[A/G]TGAGAATGGGATTGT | 114792 |
| rs368024830 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991997 | GGCTTCCGAGCGGCA[A/G]AAATGGCGGCCTGCC | 114792 |
| rs368030339 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962373 | TGGTAAATAATTTCA[A/C/G]TTATGTGAAAAAATT | 114792 |
| rs368041340 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071724 | ACCTCATGAATTCCA[C/T]TAAATAGTGTTGGTT | 114792 |
| rs368043006 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054568 | CTGAGTATGTTTGAT[C/G]CTTCAAAAGTTGCAC | 114792 |
| rs368053576 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920195 | AGGGACCTGGTCAAG[A/G]AAAATCCTTGGAGAG | 114792 |
| rs368069709 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071003 | CTGCTCCTTATTCCA[C/T]CAGTTACGCCCTGTG | 114792 |
| rs368085765 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042319 | AGGCAAATACATGAT[G/T]AAAATCCTCACTGGT | 114792 |
| rs368126625 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999610 | TCTGATGACAACTTT[A/G]TTTTTCTCTGTGAAG | 114792 |
| rs368132459 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051573 | CATAATCCATGGTGT[A/G]CATCTGAGATTTTTA | 114792 |
| rs368148032 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993142 | ATAGATACCATACTG[C/G]AAGTAATTTTTTCCT | 114792 |
| rs368148865 | snp | A/G | 3.30617e-05 | 0.00406568 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064733 | CTCATCCAGGTATGT[A/G]AGCTTGCATCCTGCT | 114792 |
| rs368162108 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931158 | TTCTCTTTCAAGTCA[G/T]ATAGGATTAAAATCT | 114792 |
| rs368217768 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141765 | TTCAATATTTTACTT[C/T]AAAAGAGGAAACAAA | 114792 |
| rs368223539 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950896 | TGAGAGCCCATGAGA[C/T]GATAGTGAGAAAATG | 114792 |
| rs368260010 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984556 | TTTATGAATCTGGGT[C/G]CTCCTGTATTGGGTG | 114792 |
| rs368274806 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094461 | CCTGGAGGAGAAAAG[C/T]GGCCATTCTGAGATC | 114792 |
| rs368276107 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127178 | GGTCCTCTTGGTAAT[C/G]TCAGCATACTTGTTG | 114792 |
| rs368306795 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039445 | TAATGAGTGCAAATA[C/T]ACAGTTTAATAGAAG | 114792 |
| rs368327112 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068952 | ACCTGCAAGAGGAGG[C/T]GTGCTGCTGGGATGT | 114792 |
| rs368345864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093756 | CTTAGAGAATTCTGG[C/T]AGAGGGAGGGAACCA | 114792 |
| rs368382352 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969311 | ACCACAGCCTCCTCT[C/T]CTTTTTCAAAATATG | 114792 |
| rs368389865 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973833 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCTG | 114792 |
| rs368396997 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038326 | AAACAGTTCACTAGC[-/A]AAAAAAAAAAATCCA | 114792 |
| rs368423179 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101965 | TTGGAGGCATATTGC[C/G]ATCATATAAATTCTG | 114792 |
| rs368439274 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072092 | GTATTTCTCAGGCAC[A/G]TGACCTCTCTGAGTG | 114792 |
| rs368451939 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100005 | CAAAAATTAGCCAGG[C/G]GCGGTGGTGCACACC | 114792 |
| rs368487363 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939641 | GAGGAAACACAGTGT[C/G]AACACAGTGGGGTGC | 114792 |
| rs368496591 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922460 | AAGTTCCTTCTTGCC[G/T]AAATTAGGCAGAGAG | 114792 |
| rs368512515 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029845 | GAGCAAAATGTAATC[C/T]TTGTTGATTCAGAAG | 114792 |
| rs368513798 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035618 | TATTGTATACTTGGC[A/C]GTTTTTTTCTTTCAG | 114792 |
| rs368545421 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075415 | TTTGATTATTTTATC[A/G]TATTACAAGTTATCT | 114792 |
| rs368550149 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051802 | TTTCATAAGAAGATA[G/T]CAGCCTATTGATGGA | 114792 |
| rs368558117 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119432 | ATAAGAGTTTGTCTG[A/G]AAAGGGGCTAAGGGC | 114792 |
| rs368572430 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078867 | ATTTCTGTGTCAGAG[A/G]CATGATTAAACTGCA | 114792 |
| rs368577918 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020415 | CTTCAAAATCTTGGT[A/G]ACAAGTTTATAGAAA | 114792 |
| rs368619132 | snp | G/T | 4.94368e-05 | 0.00497152 | stop-gained, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130841 | AAGCTTTATGTTCTT[G/T]GAGGCAATGACCTAG | 114792 |
| rs368631041 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005866 | ATATTTTCAGTTTTT[A/T]ATTTTTTTTAATTTT | 114792 |
| rs368644881 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075618 | TTTATTTATTGGTTT[A/G]TTTCAACCTGTTCCA | 114792 |
| rs368654924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946893 | AAAAACAAAGGGAAC[A/G]GCCATAAAATGAGCT | 114792 |
| rs368672344 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024751 | TTTAAACTGATTCAC[A/G]TCTAGTAAATGTAAG | 114792 |
| rs368689256 | snp | A/G | 6.65934e-05 | 0.00576995 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967095 | TCAGGTATGCCCTGT[A/G]GGATATGTCCTCACA | 114792 |
| rs368712620 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930757 | TAGCTTGGACTCAAT[C/G]ATGTCTTTTCTCTCT | 114792 |
| rs368713471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947385 | ATATTTAATTTGTCT[A/G]AAGTTTTTATTTTAA | 114792 |
| rs368716793 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915732 | TGTAATTGGAAAAGT[A/C]CTATGTATATATGAT | 114792 |
| rs368779554 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062621 | TTCTGAATAAAAAAC[-/AT]GTGTAGAGATCAATT | 114792 |
| rs368816167 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940109 | ATTAATGTTGGTGCC[A/C/G]TTTATATGGGTTATA | 114792 |
| rs368819640 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122864 | ATGCCACAGCCTGTC[A/C]TGAAACTCTTCCCTT | 114792 |
| rs368826473 | multinucleotide-polymorphism | AA/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044551 | TATTCCTTCTTTAAT[AA/TT]TCTGAAAGAGTTTTA | 114792 |
| rs368840117 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984773 | ATGTGTGTCTCTGCA[C/T]GTGAGATGGGTTTCC | 114792 |
| rs368869557 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017310 | TCAGAGACAGATAGC[A/T]TAGCTAATTTCAGCT | 114792 |
| rs368873090 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032009 | TTGTATTTAAACCTA[C/T]AACAACCCTGTGAAG | 114792 |
| rs368885663 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044419 | TGCTAGTATTTTCTT[C/G]AGGAGTTTTGCAGCC | 114792 |
| rs368913442 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078083 | TATAAGCAGCTGATA[C/G]AATTTTTAAATTTCA | 114792 |
| rs368934384 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989028 | GTTAATGGGTGCAGC[A/G]CACCAGCATGGCACA | 114792 |
| rs368979411 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122760 | ACCTATGAGGAATGT[A/G]TCATCATCACTGTTT | 114792 |
| rs368989725 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136601 | CACATAAAGGAGCAG[A/C]TGCGTAAGTGTGCAA | 114792 |
| rs369017844 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056294 | GTATTTTTAGTAGAG[C/T]CGGGGTTTCACCATG | 114792 |
| rs369023204 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010198 | TCTATGCCATGCTCC[G/T]GGTTCACTGCAGATT | 114792 |
| rs369039512 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030310 | GCTGTAACTAATCTT[A/G]TGTCTGCATGACAAG | 114792 |
| rs369065807 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987554 | ATAGATTCAATGCCA[C/T]CCCCATCAAGCTACC | 114792 |
| rs369097317 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096391 | TACTCCCACCATTGG[C/T]TCGTTGGTCTCAGCA | 114792 |
| rs369129832 | in-del | -/CAAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968391 | AAACAAAAACAAAAA[-/CAAAA]AAAAAAACATCTAGC | 114792 |
| rs369141043 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019094 | AAATTGATAATCTAG[C/G]CTCCTCCTATCATAT | 114792 |
| rs369151062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032244 | CCAAAAGATACTTAC[A/G]TAAACAGGATAAAAT | 114792 |
| rs369172099 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085785 | GCAATAGAGAGCAGC[C/T]TGGATCTCGAATGAA | 114792 |
| rs369200427 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009226 | TCAAGCACAATAGAG[A/T]GGAATTTTGGTTTAT | 114792 |
| rs369234220 | snp | A/G | 0.000578976 | 0.0170045 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132782 | TTTGAAGTTTGTTCA[A/G]GTGGTTCAGCGAGGT | 114792 |
| rs369239331 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079340 | CACTGGCTTGGGAAG[G/T]GTGGGCTGAAAGGCC | 114792 |
| rs369268980 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896857 | GATAGACTAAGGAAA[A/G]GAAAAAAGTCACAAT | 114792 |
| rs369297093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117558 | AGGAATCCAGAAAAT[C/T]CTGCTGCGTGTACAT | 114792 |
| rs369305145 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983105 | GCGTTGTTGAATTTT[C/G]TCAAAGGTCTTTTCT | 114792 |
| rs369325183 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013777 | ACCTACTAAGGCAAA[A/G]GAAGAAAACAGCGTA | 114792 |
| rs369346492 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949323 | CTCCAGCTCTGATAT[A/T]CTAGTTAGTCAGTTT | 114792 |
| rs369348470 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072578 | GCTTTTTTTTTTTTG[A/T]CAATTTACTACCCAT | 114792 |
| rs369354741 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041039 | TTATAGCATATGAAA[A/G]TGAACTAATACAATG | 114792 |
| rs369378656 | snp | C/T | 1.66067e-05 | 0.00288151 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976099 | TGATGGCATCCTCTG[C/T]GACATCACCCTGATT | 114792 |
| rs369382399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931451 | ATATTGTAGGATCCC[A/G]TAGACTGAGCTAAGC | 114792 |
| rs369385579 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125789 | CTCAAAAAAGAAAAA[A/G]TTACCGTCCTACATT | 114792 |
| rs369394705 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984971 | TCTTCCTAGCCTTGA[A/T]GGTCTTTACAATTTG | 114792 |
| rs369398253 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946891 | GAAAAACAAAGGGAA[-/C]CGGCCATAAAATGAG | 114792 |
| rs369411177 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020322 | AAAAGAAATACAATA[C/T]AAAAAATGAAAAAAG | 114792 |
| rs369411683 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085254 | GAAGAGCCGCCCAGA[A/G]GAAGTTCTAACGCTT | 114792 |
| rs369447149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932832 | CACCTTGGGCTTCCA[A/G]AGTGCTGGAATTAGA | 114792 |
| rs369480673 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065080 | CTGGTTATGGAAATA[A/C]TCACAAATGCAAGAA | 114792 |
| rs369481227 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951200 | AGACTTCAACAGGCT[A/G]AGTAGGACAGGGAAG | 114792 |
| rs369517086 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063492 | GGTACTGATACAGAT[A/G]TAGGTAGATAGGTTG | 114792 |
| rs369526756 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091431 | AGCCATGTCCTGTGG[A/G/T]GTACTACTATTGCCT | 114792 |
| rs369527875 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123743 | CTATAAAATATACTC[A/G]ATAGAGGAAGGCATG | 114792 |
| rs369533085 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970002 | AGTTGTATAAGCCAG[A/G]AATATAGGTGTCTTC | 114792 |
| rs369562307 | snp | C/G/T | 0.0119135 | 0.0762987 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942805 | TGATGCCACCACCTC[C/G/T]CTTTCTACCTCCATC | 114792 |
| rs369565910 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108896 | ATACCTGCTTAAATT[A/T]AAAAAACAGAGTGAA | 114792 |
| rs369596160 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072211 | ACCCCCTTAACTTGT[G/T]AAATCTCTCTCATTG | 114792 |
| rs369597389 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985680 | AGCTACTGAGGCTTG[G/T]GCATTTGTCACGTAG | 114792 |
| rs369633174 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978915 | GTTGAGCACTTTTTT[-/T]ATATGCTTGTTGGCT | 114792 |
| rs369640379 | snp | G/T | 3.29571e-05 | 0.00405924 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139224 | AACATAGCTCTGAC[G/T] | 114792 |
| rs369646859 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104385 | CTGAAGTATGTACTT[C/T]AAAACATGTGTTTAA | 114792 |
| rs369647726 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068031 | ACACACACACACACA[C/T]ACATACACACACCAT | 114792 |
| rs369652068 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906375 | ATGGGTAAAGAGACC[A/G]GGAGAATGGGATATA | 114792 |
| rs369652835 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060898 | ATCCCCACCAAAATG[-/A]GTGTAGAGTTTCAGC | 114792 |
| rs369669394 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082289 | TATCTAAAAGAGGAG[A/T]TACAGGAGTAGATGC | 114792 |
| rs369669992 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981548 | TTAGAATCTCAATTT[C/T]CTTCAGTTCAGCATT | 114792 |
| rs369670517 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928450 | CAACTGCGGATGGGT[A/G]GGAGGGGATGGAGGA | 114792 |
| rs369708629 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078857 | AATGTGTATAATTTC[C/T]GTGTCAGAGGCATGA | 114792 |
| rs369720132 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974943 | TGCTGGCCAGAATCA[C/G]GGCTTGATGGCTCTT | 114792 |
| rs369734849 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939367 | GTGAGGAAGATAGTC[A/C]GGAACTTGTCATCTC | 114792 |
| rs369770987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079944 | ATTCAAAACCACTAC[C/T]GCTACCTGGATACTT | 114792 |
| rs369795626 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036660 | GAGGAATGTGCAGGG[G/T]CACTGGTTTTGGGGA | 114792 |
| rs369808175 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987485 | AGAACATTCCATGCT[C/T]ATGGGTAGGAAGAAT | 114792 |
| rs369815794 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038239 | AGTGTAGAGCAAACC[-/C]ACAGAATGGGGACAA | 114792 |
| rs369818687 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977314 | TCACACAGTTCCTAA[A/G]TGGCAGATCTGGAAT | 114792 |
| rs369819487 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006585 | TGCAGACTTGATTGT[A/G]TAGTTGCTCTATATA | 114792 |
| rs369823578 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022650 | AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 114792 |
| rs369824879 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951523 | TGTACCTTAACCATC[A/G]CTGGTAAGGTAGTTA | 114792 |
| rs369832119 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936875 | GCCTGGAATGCCCTG[C/T]CTCCTGCCTACCCGC | 114792 |
| rs369842413 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969543 | TATTTCCATGCCTAC[A/G]TTGTCTAGTGGAGAC | 114792 |
| rs369844253 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958898 | GGCCTCAGGGATGGA[G/T]TGTTGGGAGGTGATG | 114792 |
| rs369865526 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982253 | GTTGCGTGAATATAT[A/G]TTTAGTATAGTTATG | 114792 |
| rs369866318 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067420 | AAAAGGAAAGCTGGG[A/C]AATGTATTTAATGCT | 114792 |
| rs369904355 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118281 | CATTTAAAAATATAA[G/T]TGCCTTATCTTTTTG | 114792 |
| rs369915356 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917504 | GAGGTCAGAGAGAGA[A/C/T]GCTGGCAACAGAAAA | 114792 |
| rs369925872 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039106 | AAAAAAAAAAAAAAA[-/G]AAAAAAAGAAAAAGA | 114792 |
| rs369926564 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083626 | ATTTTTTAAAAGTCT[A/G]GAAGTATATATACAA | 114792 |
| rs369928536 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061427 | TTGTTATTAAGACAT[G/T]TTGTCTTGTCCACTG | 114792 |
| rs369929538 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025199 | ATGATTCTGTTTATC[A/G]TCTTTGTAAAAATCT | 114792 |
| rs369945640 | snp | C/T | 1.69235e-05 | 0.00290886 | intron-variant | KLHL32 | GRCh38.p7 | 6:97139106 | ACACAAGCTTCTTCT[C/T]TTCCTCTTTTGTAGG | 114792 |
| rs369947593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009763 | TAAAGCATCAGACTG[A/T]TTCATATTTAAGAGC | 114792 |
| rs369951839 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054377 | CTTAATGAACACCTA[C/G]TATATGCTAAGGACT | 114792 |
| rs369958494 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974077 | ATTGTTATATTCTTG[A/G]TGATAGGTTCTCAAA | 114792 |
| rs369968936 | snp | C/T | | | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064702 | GTTGGAGCTTCTCAA[C/T]TTATGCTCCCACTAT | 114792 |
| rs370009318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106735 | GGTGACAGAGGAGAC[C/T]CTGTCTCAAAAAAAA | 114792 |
| rs370025930 | in-del | -/CTTTA | | | splice-acceptor-variant, intron-variant | KLHL32 | GRCh38.p7 | 6:97132647 | ATTCAATTCTCTTTA[-/CTTTA]GGCCAAAATGAATCT | 114792 |
| rs370032788 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031958 | TCTATATAACATTTA[C/G]TATGTGCCACATATT | 114792 |
| rs370032981 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126286 | TCCCATATCCTTGAT[A/G]TTTTATTATCTAACA | 114792 |
| rs370035898 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917026 | TAACAACAACCTTAG[A/G]AGAACCCTATGTATA | 114792 |
| rs370039034 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921633 | AAAACCACGACACTG[G/T]CATTAAGAATGACAA | 114792 |
| rs370039412 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111037 | AAAAGTCTTGGGGGG[G/T]GGGGGTCTTAGCCAA | 114792 |
| rs370045478 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141225 | AAAGCTCTAAAAATA[A/C]GCTTGCCCAACTAAT | 114792 |
| rs370052081 | snp | A/G | 0.000345915 | 0.0131468 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897826 | ACATTATGCGCTCAG[A/G]TTCAGGCCGCACGTG | 114792 |
| rs370062586 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048080 | TAGTTAGCTTCCTCT[G/T]AATTTCCGGAGAGCT | 114792 |
| rs370085668 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956904 | AAAAAATAGTAGCAC[A/G]TTAAGGTATATAGTG | 114792 |
| rs370087278 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972235 | TAAACATGTAATCAG[A/T]ACAGAAATATTGAGC | 114792 |
| rs370132103 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078982 | TTCTCAGCTTGTATC[A/G]TCATTGGCACACAAG | 114792 |
| rs370149997 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903974 | TAGAGAATCTGGCAA[A/G]GACTATTAGATCTAA | 114792 |
| rs370154434 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106152 | TGTTTCACATGAACA[A/G]TAAAGGAATTAGAAT | 114792 |
| rs370156624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928587 | ACCAAGTATTATATT[A/C]TCTATACAGAGACTG | 114792 |
| rs370231620 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923782 | ATACAGTTTACTCCA[A/G]TTTAGTTACACTCTT | 114792 |
| rs370236089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058712 | TTTTTTGTTCTTTGA[C/T]CTCTCCTTTCTTTCT | 114792 |
| rs370243164 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991282 | TGCTCAGCTGGGGGT[C/G]GGGTGTCTGCTCTGC | 114792 |
| rs370262579 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034104 | AAATTATTGCTTAGA[C/G]CAATGTCAAGGAGCT | 114792 |
| rs370267949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103460 | CCTTGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 114792 |
| rs370277937 | snp | A/G | 2.17644e-05 | 0.00329875 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064605 | GTAACTGATAGTTTT[A/G]TTTTTGTTAACAAAC | 114792 |
| rs370298566 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024312 | CTGCTGTAATAGAGT[C/G]TGCACATGGTGGTGG | 114792 |
| rs370331632 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135302 | ACAAATTTGTTAATT[C/T]TTTTTTTTTTTTTTT | 114792 |
| rs370348788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097497 | GCACGGATATAGTTT[C/G]GCTGTCAATCATTGT | 114792 |
| rs370352878 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909378 | ACCTTCTTTCTGTCT[C/T]GGGACCCAGTTTTTA | 114792 |
| rs370386614 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037813 | AGCCTGGTACTGGCA[A/T]AAAAACAGACACATA | 114792 |
| rs370395475 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004108 | GATTCTTCCTATTCA[G/T]GAGTATGGAATGTTT | 114792 |
| rs370406468 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966513 | TATTTTTTCCACCTA[C/T]TTTTCAGAAATCTGC | 114792 |
| rs370424386 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902404 | TATGTTTTATTTTGA[A/G]AAGTGTCTGGGCATG | 114792 |
| rs370428731 | in-del | -/CAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934461 | TAACAACAACAACAA[-/CAA]AAAAATAGCAAGTTA | 114792 |
| rs370442801 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064892 | AGTTCCTAGGAGGGC[A/G]GCTGCAGCTCTTGCA | 114792 |
| rs370472735 | in-del | -/GA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993986 | TTTGCTCTACATAGA[-/GA]TACTGTATCTTCCAG | 114792 |
| rs370475276 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081080 | ACCATTGAAAACATG[A/C]TTTGTTTCTGCTCCA | 114792 |
| rs370478130 | snp | A/C/G | 0.000798403 | 0.0199641 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141761 | TCACTTCAATATTTT[A/C/G]CTTTAAAAGAGGAAA | 114792 |
| rs370481939 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930888 | CTCTGGGCTCTATCA[C/T]AGGATCTCTTCAGGG | 114792 |
| rs370486249 | snp | C/T | 0.000437904 | 0.0147905 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966981 | TGCACCCTTTTCTCT[C/T]GTCTTTTTATTCAGC | 114792 |
| rs370488922 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899408 | CAATTCGACTCACTG[C/T]CTGTTAAAATATTTT | 114792 |
| rs370512220 | snp | A/C | 1.64974e-05 | 0.00287201 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114277 | TCGCTATGACCCCCG[A/C]AGTAATTCCTGGGCA | 114792 |
| rs370569677 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994712 | ACCATTTTAAAAGAA[A/G]GTGAAAAAACACATT | 114792 |
| rs370573165 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131152 | TCTAGTTTCTCAGGG[C/T]CTATATTACTACCAT | 114792 |
| rs370612861 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131341 | TATTTCTTGTGAGTT[C/T]AGGAGTTTAGGAGCA | 114792 |
| rs370629593 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055806 | TGTCTAAAAAAAAAA[-/C]AAAAAAAAAAAAAAA | 114792 |
| rs370649171 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948168 | AAGTCTAGCTATTCC[A/G]TGTTACTAATGCTAG | 114792 |
| rs370657432 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999353 | GTGAGGCATGATTGT[A/G]CCACAGCACTCCAGC | 114792 |
| rs370679148 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122839 | ATATAGTCATGTAGG[A/T]CCCATGTTAATGCCA | 114792 |
| rs370735481 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040589 | TCTGTACTCAGACAC[A/G]TTCCCAGGTGATCCT | 114792 |
| rs370740087 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906795 | TCTTGGTGTAGTTAA[C/T]CCTTTTTAGAGCTTT | 114792 |
| rs370773058 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910650 | TGTTGATTTTTAAAA[A/T]CAATTGTATCTTAAT | 114792 |
| rs370774674 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027641 | CATTCACAAGCTTAG[A/G]ATGATTTACTCTTTC | 114792 |
| rs370779354 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044540 | GAATTTGAAAGTATT[A/C]CTTCTTTAATTTTCT | 114792 |
| rs370800991 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130513 | AAAATGCACTATAAA[A/G]TGCAACACAAACTAG | 114792 |
| rs370805868 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039385 | TACCCTACCCAGTAG[G/T]CTGGGAAGGGTCGTA | 114792 |
| rs370806644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135259 | GCGTTTATTCCTTTG[A/G]CTGGCACACTGGTCC | 114792 |
| rs370817474 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070545 | GAGGCACACTGGCTG[G/T]CCAGGGAAGTCATTT | 114792 |
| rs370837329 | in-del | -/CCCCCC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968956 | TGTTTGAGAAAGCCA[-/CCCCCC]CAGCCACAAAAACAA | 114792 |
| rs370872509 | in-del | -/CA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051032 | AACAAACAAAAAACA[-/CA]TGTGTTTGAACAATA | 114792 |
| rs370892109 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073273 | TCTGTAAAAGATATT[A/C]TTCCTCTTAGCCACT | 114792 |
| rs370903474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067119 | ATATACCATTGCCCT[C/T]CAGTGCTCACTACAA | 114792 |
| rs370913220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977647 | GAGCAATTTGTTGAT[G/T]GGTTTGAATATTTCT | 114792 |
| rs370926707 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992216 | GGTGTCCGGTACCAG[C/G]GGATCCATGGCTCCC | 114792 |
| rs370941248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080951 | CATAGGAATTTTGCT[C/T]ATGCTGCTTCTTTGG | 114792 |
| rs370941469 | multinucleotide-polymorphism | CC/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928203 | GGAGATCAGGTCAGT[CC/TT]CTAGGTAGTAGGGGG | 114792 |
| rs370962765 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016301 | CAGAGAGGGGGACTG[C/T]ACCCTGCGAAGCCAC | 114792 |
| rs370969523 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108360 | GTTCCAAGAATAATT[C/T]TTTTCAAGCTTAAGC | 114792 |
| rs370973849 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115991 | TTCATTTGGACTTTG[A/T]CTGTTCTTCTGCTGT | 114792 |
| rs370994779 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030470 | TTATATACTCACAAA[A/C]TAGGTTTTCAATTAG | 114792 |
| rs371015140 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007590 | CACAGTTCTTGCACT[C/G]GTTCTTTCTCATGTG | 114792 |
| rs371015681 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970511 | GCTCAAGTATTATTT[A/C]TTTAGGGAGGCCAGA | 114792 |
| rs371040722 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953559 | TGCTTGAACCTGGGA[A/G]GTGGAGGTTGCAGTG | 114792 |
| rs371060588 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934244 | ATTACTGGATCTTCT[A/G]TACTTACTGTGTGAG | 114792 |
| rs371084680 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137645 | GTTCAAGCCATTCTC[C/T]TGCCTCAGCCTCCCG | 114792 |
| rs371090551 | snp | G/T | 1.64868e-05 | 0.00287109 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041492 | CTTTCCTCACCTCAG[G/T]CAATGTTCAGTCTTT | 114792 |
| rs371096515 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967359 | CCCTCAAACATGAGG[C/T]ATGCTAGTATAAAGG | 114792 |
| rs371104176 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983900 | TCTGCTCTGATCTTA[C/G]TTATTTCTTGCCTTC | 114792 |
| rs371107569 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127476 | AGGTAAGAATCATGT[A/G]AGAACACCTCATTAT | 114792 |
| rs371111753 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984606 | TAGCTCTTCTTGTTG[A/C]ATTGATCCCTTTACC | 114792 |
| rs371112350 | in-del | CC/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932564 | ACAAAGTTGTCAATT[CC/T]CCCCCCCCCCCTTTT | 114792 |
| rs371120222 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960441 | CTTTGAGTTACTCAT[A/G]ACTAGGGGCTCCCAC | 114792 |
| rs371132978 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963246 | ATTATCAAAGGAAAA[C/G]GGGTTTGGGGCTTCT | 114792 |
| rs371155027 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085505 | TTGGAGAACACTGGC[C/T]CTTGAGGCTCAGAGC | 114792 |
| rs371169611 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009375 | AGGCTTTGCTTTTCA[A/T]ATGTAAATGTTTAAT | 114792 |
| rs371174497 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039969 | TTAAAAATTAAGACT[A/G]TATTAAATTATCATA | 114792 |
| rs371179405 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020654 | ATCTCAATATAGATA[C/T]AAAAATTATAAATAA | 114792 |
| rs371186318 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069264 | GTTTACTCAGCATCC[C/T]TTGTCTTCGTTAAAT | 114792 |
| rs371196337 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936166 | TATAATTAAGAAATT[A/G]TAAGAAAATGAGATA | 114792 |
| rs371250783 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962234 | CAACTTTGAAACATT[-/TT]AATAAAAATAAAGAC | 114792 |
| rs371297758 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025464 | CCTGCTACAATTATG[A/G]GAATTAGCTAACTTC | 114792 |
| rs371322892 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095288 | TGCTGGGACTATGTA[C/T]TCTTTGGAGTGAAGC | 114792 |
| rs371325923 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123594 | ACTGTGGCACTTCAA[A/G]GTTAGAGAAAACTTG | 114792 |
| rs371329994 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909762 | GAGTTATTGCCAGAA[C/T]ATCAGCACATTCAGA | 114792 |
| rs371338283 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138153 | AAATGGGGCGAGAGC[A/C]GCTCTCCTGAAGAAA | 114792 |
| rs371338288 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943385 | TTTCCAAGAAGAAGT[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs371367214 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995881 | ATTATGTACTATGTG[A/T]GGCAGCCCCCTTACC | 114792 |
| rs371379772 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043674 | TATTAATTTATATTC[C/T]CACTAACAGTGCACA | 114792 |
| rs371396050 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012577 | ACCACGAAGTTTGTG[A/G]TACTATCACAGTAGC | 114792 |
| rs371401478 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924309 | GGAGTCTGGGGGCGA[C/G]CAGGCTGGGTTCCCG | 114792 |
| rs371423888 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919259 | AGTAATGAGGTTATC[A/G]ATAATCAATTTCAGT | 114792 |
| rs371440388 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113900 | GTTGCCCTGTCCCAC[C/T]CCCTTGTCCAAGCAA | 114792 |
| rs371469297 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914459 | GTAATTGCATTTGAT[A/G]TTGCTAGCATTTGAA | 114792 |
| rs371497714 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981025 | GGGGGCAGGCGGGGG[A/G]AAAGCCCCTCATAAA | 114792 |
| rs371522926 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037745 | AGCAAAAAGAACAAA[A/G]ACATTACACTATCAG | 114792 |
| rs371525304 | snp | A/T | 1.64779e-05 | 0.00287031 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139183 | TACACTCCCTTTTGC[A/T]TCCAATGGAATAGCA | 114792 |
| rs371559276 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007606 | GTTCTTTCTCATGTG[C/T]ATGGGCTGATGTTTC | 114792 |
| rs371565076 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097370 | AAGGTTGATTATGAT[A/G]GTTTGTGCCTCTTTC | 114792 |
| rs371568812 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076818 | AACATTTCTAGGCAC[A/G]TACCTTTATTTAAAT | 114792 |
| rs371577277 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985604 | CTAAACTTCTCTTCT[C/T]GCTTCATTTCATTCA | 114792 |
| rs371577539 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055774 | CTGCACCCCAGCCGA[C/G]GTAACAGACTGAGAA | 114792 |
| rs371578797 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105048 | TAGTATTGCATGGCA[A/G]ATCGCAACACCTGCT | 114792 |
| rs371615327 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115574 | CACCCACAGACCCAT[C/T]ACACCCCTCTGGGCT | 114792 |
| rs371646753 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108589 | TCTTTGCCATTTTTT[-/T]AATTATTTATTTGAA | 114792 |
| rs371663899 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035043 | AAGTTGAATAAAAGC[A/G]GTCTCTCGTCTTCTC | 114792 |
| rs371706134 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135284 | TGGTCCTACAAAGCA[C/T]AGACAAATTTGTTAA | 114792 |
| rs371713490 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133030 | TTCCCTTTCTCATAA[A/G]CCAAAAAATTCTAAA | 114792 |
| rs371719741 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112425 | TAGGTGCTCCATAAA[C/T]GAATTGTGGTTTTTT | 114792 |
| rs371736502 | snp | A/G | 1.65343e-05 | 0.00287521 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132772 | AGAAGTTCCTTTTGA[A/G]GTTTGTTCAAGTGGT | 114792 |
| rs371749579 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969890 | GCTTGGATGTCTTAA[A/G]GACAACTCAAACTTA | 114792 |
| rs371761271 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966339 | AAAACAAAGACACGG[A/G]ATGGGGGCAGGGACT | 114792 |
| rs371772160 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977282 | GTAATTTGCACTAAC[G/T]CAGGATCAGTAAGAA | 114792 |
| rs371772184 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021361 | AGACCCAGGAGAGCC[A/G]ATGATGTAGTTTCTG | 114792 |
| rs371775657 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941583 | ATGATGTGATGACCA[A/G]AAAACAATCAAGGTA | 114792 |
| rs371816437 | in-del | AA/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105771 | AGACCAAGACAAAAA[AA/T]AAATACTTGTTACTT | 114792 |
| rs371855665 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051596 | GATTTTTACTTTGCC[A/G]TGGTGGGTAAACAGC | 114792 |
| rs371861397 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046186 | TGAAAAAGCCAGGGG[A/G]CAGCACTAGGCACTT | 114792 |
| rs371891203 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981799 | ACTTCTACCTTAATT[C/T]CATTGTTTACCCGAA | 114792 |
| rs371896883 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929502 | GAGCAGAACTTAAGA[A/G]TTTATCCTAGAACAT | 114792 |
| rs371905888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976332 | GAATGCTTCCTGGGG[C/T]CCCATTGGGTCCTCT | 114792 |
| rs371908220 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112603 | AGGCACGTGCCACCA[C/G/T]GCCCAGCTAATTTTT | 114792 |
| rs371939067 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940449 | GATTCAAGGAGAGAG[A/C]ATTTACTGATGCAGA | 114792 |
| rs371962629 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024895 | TATATTGAAATATCA[C/T]TTTATTTTTCTGCCA | 114792 |
| rs371962822 | snp | C/T | 1.64795e-05 | 0.00287045 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139229 | GCTCCATATTTTACA[C/T]GCCCTAACCTTCAAA | 114792 |
| rs371964519 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990262 | ACATTCAGTTGCCTC[G/T]TTTCTGGATGTTTTC | 114792 |
| rs371965496 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048142 | AAGAGGTTCCAGAAA[C/T]CCAGTGGAGAGATAA | 114792 |
| rs371997412 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976846 | TCAAGTAATCTGCCC[A/G]CCTCGGCCTCCCAAA | 114792 |
| rs372005187 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989321 | CCCTTAGCATTTGCT[G/T]GTCTGAAAAGGATTT | 114792 |
| rs372018624 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045720 | AGTTGATGTGTATGT[A/G]CGTGTGTGTGTGCAC | 114792 |
| rs372020653 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015390 | AGAGACTTGTTGAAT[A/C/G]GACTTTACCAAAATG | 114792 |
| rs372026250 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021085 | ATTTATTATAAGGAG[C/T]TGGCTCATACGATTA | 114792 |
| rs372026708 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093345 | TTGAGTCTCTCATCA[A/C]CCTTGTTAAGGTTGA | 114792 |
| rs372026976 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135965 | GAAAATGCTTAACAG[C/T]GGAAATTCCTAAGTA | 114792 |
| rs372047144 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043012 | CTCCTTCCCACTCTC[A/G]TGCTTCCTCTCTTAC | 114792 |
| rs372068646 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071258 | CAAAGGTCACCAAAG[C/G]CTCCTTATTGTCTGA | 114792 |
| rs372070204 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018951 | TTTTTTAAATGTAGA[C/T]GGAAGATATGGATAG | 114792 |
| rs372072947 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902745 | TTCAGTCTGTAATCC[A/G]TCTTGAGTTGATTTC | 114792 |
| rs372088351 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983696 | AGTGTTCTCTGATGG[C/T]AGTTTGTATTTCTGT | 114792 |
| rs372124018 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048417 | GAGAATGCTTCAATA[C/T]GATCTTTACAAGGAA | 114792 |
| rs372125237 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968403 | AAACAAAAAAAAAAA[-/C]ATCTAGCCCAAAATG | 114792 |
| rs372125999 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059954 | GAGGAAATGTAATCA[C/T]TTATTCTCATAAATG | 114792 |
| rs372137098 | snp | A/G | 1.64779e-05 | 0.00287031 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897721 | TCTGGGAGCGACAGA[A/G]GGCTTCATCTTGCTG | 114792 |
| rs372168916 | in-del | -/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095875 | TCTTCTGAAAAACAA[-/AA]CAAAAACTCTGAGAT | 114792 |
| rs372185422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028277 | CCAGGGACCACACCT[G/T]AAGTAGGGAAGGGCC | 114792 |
| rs372218919 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897135 | TAGCCATGTTGGCCA[A/G]GCTGGTCTCGAACTC | 114792 |
| rs372222548 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914252 | TTCTAACCTACAGAA[C/T]TGTAATATAATACAT | 114792 |
| rs372257163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047413 | GGTGGAGGGCATAGA[A/G]GCCAGGCTGCTCTTG | 114792 |
| rs372277886 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029365 | GATTTTAGAAAAAAA[-/A]CAATATGTAACATAA | 114792 |
| rs372307199 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065957 | ATGATTATTTGAGCA[C/G]ATTTAATCTAACAGT | 114792 |
| rs372315425 | in-del | -/TGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981357 | ATAGAGGTTTGTAGT[-/TGT]CTTTGAGGTTTTTTT | 114792 |
| rs372345654 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094519 | TTCTTGAGCTTTTTT[A/T]ATGCTCATAATACAG | 114792 |
| rs372353362 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110084 | AATTCCAAGATTAGG[A/G]TAGAGAAAATCTAGG | 114792 |
| rs372402091 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133617 | AAATTCCATGTTGTC[G/T]AAGTTTTCAAAATTG | 114792 |
| rs372402141 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094499 | GGAGAAGCATTCATA[C/T]ATCATTCTTGAGCTT | 114792 |
| rs372407688 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907282 | ATGGCAAATCTAATT[C/T]CTTCTATATACTTTC | 114792 |
| rs372439946 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938452 | TTCCGGCATGCTTCT[C/T]GTGTCCTGCAGATAC | 114792 |
| rs372498091 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078927 | CCAGGGAGCCACGGC[A/G]GTAGCCAAAACTAAG | 114792 |
| rs372502372 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936965 | CATTGTGATCACTGT[C/G]CTTAAAATTACAACC | 114792 |
| rs372511840 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918667 | GATAAGTGGCCTAAA[C/T]ATGAAAGAAAATTTT | 114792 |
| rs372513778 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960806 | TATGACAGCTGGAAG[C/T]GGGGGCTTCTGGGTC | 114792 |
| rs372549179 | snp | A/G | 1.64762e-05 | 0.00287016 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897845 | AGGCCGCACGTGGGA[A/G]CACCGGCGCAGGACA | 114792 |
| rs372554538 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060787 | ATAATTTCTCCTACC[A/T]GGTACCCATCCCCTT | 114792 |
| rs372555206 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075760 | ATTTATAACTCAGTT[A/G]TAATCAAAATAGGAA | 114792 |
| rs372561338 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075849 | GGAATTTCTAAAGCC[A/G]TATACACTTTTTTGT | 114792 |
| rs372595851 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997036 | GCGATGGGGAGGAAA[A/G]ACAAGAGTGAGTGTG | 114792 |
| rs372597727 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929299 | TGCTCTTCACAGATA[C/T]ATTTGGCAAGTAATG | 114792 |
| rs372635399 | snp | A/C/G/T | 0.000148299 | 0.00861002 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897850 | GCACGTGGGAACACC[A/C/G/T]GCGCAGGACAACTCC | 114792 |
| rs372656806 | snp | C/T | 3.29516e-05 | 0.00405891 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130883 | GACCGGATCCTTGTG[C/T]GCCATATAGATTCTT | 114792 |
| rs372678106 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019987 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTAGAGTGC | 114792 |
| rs372689083 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113253 | GGGGGAGTCTTTTTT[-/T]CTTTCTAAATCATTC | 114792 |
| rs372691435 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114134 | GCCATTGCCAACTGG[A/G]GTGAGCTGGCTCCCA | 114792 |
| rs372707801 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078044 | AGCCTTATACTTACC[A/G]TATCCTACTTGCTAC | 114792 |
| rs372748411 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100631 | CTTTCTGGACATCTA[A/C]ACTCATCATAGTACC | 114792 |
| rs372779052 | snp | C/T | 1.66796e-05 | 0.00288782 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064776 | ACATTCCTTTCCCCA[C/T]AGTCATAAGCTGGCC | 114792 |
| rs372786322 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031945 | ATAGCGACAGTTTCT[-/AC]ATATAACATTTACTA | 114792 |
| rs372799357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049829 | TGAAACAAACAAGCA[C/G]ATTAGTCTGCTTCCT | 114792 |
| rs372823441 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005942 | GTGGTATGTGCAGAA[A/G]AGAAGAATGTATAGT | 114792 |
| rs372924935 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942537 | TTAATTTGAAAGTAT[A/G]TGAATGATAGAAGCT | 114792 |
| rs372930745 | snp | A/G/T | 6.59174e-05 | 0.00574059 | missense, synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132693 | CCATAATGGGAGAAT[A/G/T]TATTTAGTTGGTGGA | 114792 |
| rs372934978 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984866 | TGGAGCATTTAGCCC[A/C]TTTACATTTAAGGTT | 114792 |
| rs372964003 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134282 | CAAAGCCACACACAC[A/C]TGAAGAGCCACATAA | 114792 |
| rs372972229 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968102 | TCTGAAGCTATTAGA[A/G]GTGATTTGTTCCAGA | 114792 |
| rs372975724 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043225 | AATGGACTAAGAAAA[C/G]ACCCTCCCCTAGCCT | 114792 |
| rs372985990 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037335 | TACAAGGAATAATGG[G/T]TCATCAGTTTATATT | 114792 |
| rs372993717 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938434 | TCTCTTCTGGGCTCC[A/G]CCTTCCGGCATGCTT | 114792 |
| rs372996783 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971312 | GTCAAAATTCTTTCC[A/G]TGAACATCAAACCCT | 114792 |
| rs373001058 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030901 | GTTTTGAAGATGATA[A/T]TGGTTGATTCATTCA | 114792 |
| rs373043895 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967101 | ATGCCCTGTAGGATA[C/T]GTCCTCACATGCCGT | 114792 |
| rs373063574 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065994 | GTAAATGGTTAATGA[-/T]TTTTTTTTTACCTTA | 114792 |
| rs373083759 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962519 | TCCTTGAAGGATTGC[C/T]GCTATACACATTCTT | 114792 |
| rs373086183 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943119 | ATACACATATACACA[C/T]ACCAGCATATAGACA | 114792 |
| rs373101584 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091402 | CAAATAGTTATTGAG[A/T]GCCTGCTCTACCCAG | 114792 |
| rs373114335 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904640 | TTTTTAATGAAGCTC[A/G]ATCACTGATAATAAA | 114792 |
| rs373154180 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096883 | CTGCCCTTGGTTTTA[G/T]CTTCTCATCATTTAA | 114792 |
| rs373163332 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076735 | AAAAGTAGCACACAG[C/T]TCTGAAAAGTTCAGG | 114792 |
| rs373167798 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084260 | AAGTAGGAAATAGCC[C/T]ACTCTCATTCTACTT | 114792 |
| rs373174127 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113410 | ATGACACCTCCCACC[A/G]TTGACATTTCCTGGT | 114792 |
| rs373191243 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969321 | CCTCTCCTTTTTCAA[A/G]ATATGGTTGTACTTT | 114792 |
| rs373211925 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940853 | CATTCATAGAACAGC[C/T]GAGAGAAAAGATATA | 114792 |
| rs373212198 | snp | C/T | 4.98235e-05 | 0.00499092 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132792 | GTTCAAGTGGTTCAG[C/T]GAGGTTACATTTTGC | 114792 |
| rs373221113 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908092 | GGTGTTGTGCCTTCT[A/G]TAACAGCTAAACAAG | 114792 |
| rs373236147 | snp | A/G | 6.73786e-05 | 0.00580386 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976134 | AGGAACAGAAATTCC[A/G]TGCTCACAAGGCAGT | 114792 |
| rs373247860 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995421 | TTTAACTTTTCTCCT[C/T]CTCTGGCTGTTCTTT | 114792 |
| rs373270414 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042880 | TCGGGTCTGTAGGTG[A/G]ATGTTGGGGTCATGT | 114792 |
| rs373301905 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140402 | GGTTATGTCAATCTT[G/T]AGTGCTTGTGGAATT | 114792 |
| rs373312652 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040482 | CAAATTCAAGTGGGC[A/G]TGAGAGTCACCTGGA | 114792 |
| rs373324825 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080862 | GAGAAATGTGATTGA[C/T]GGTGACATGGAGAGG | 114792 |
| rs373332675 | snp | G/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897518 | GTCACCGGCCTGGCG[G/T]CTCCCCCTTCCAACG | 114792 |
| rs373351494 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949424 | ATCCAGTGTCTCTGG[A/G]TTCATTTCTAATGTT | 114792 |
| rs373354159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978721 | TGAGAAATTGCCAAA[C/T]GGCTTTCCACAATGA | 114792 |
| rs373377694 | snp | A/G | 0.000153988 | 0.00877328 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896707 | GAAGCCCCAAAATAA[A/G]TAAATTGTGTATTCA | 114792 |
| rs373379205 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067429 | GCTGGGCAATGTATT[C/T]AATGCTAATTGATGG | 114792 |
| rs373384225 | snp | A/G | 5.09489e-05 | 0.00504697 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139317 | CAGGAGGAAAACATA[A/G]CTCTGACTGTTGGAT | 114792 |
| rs373413926 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073351 | AATAATTAAATGAAC[C/T]GTCACTTTCTTTCTG | 114792 |
| rs373446958 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985080 | TGGTGGTGACAAAAT[A/C]TCTCAGTATTTGCTT | 114792 |
| rs373474934 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929816 | CAGTTTTGCAGACTT[A/G]ACTTGGAGTCAGATT | 114792 |
| rs373477313 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036160 | CATTTATTGTGTTCT[G/T]CAGCTTCAGAATTTG | 114792 |
| rs373480840 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937346 | TAGCATGTGTGGTTC[A/G]AAAGATGAAGGAGCT | 114792 |
| rs373488464 | in-del | -/GA/GAGA | 0.195102 | 0.245296 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967499 | ATAGGGATAGAGAAT[-/GA/GAGA]GAGAGAGAGAGAGAG | 114792 |
| rs373509903 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132683 | GAGTTGCTGTCCATA[A/G]TGGGAGAATATATTT | 114792 |
| rs373510087 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919109 | TCTCCTGGGAATTTG[A/C]ATCTTGGATGGAGTG | 114792 |
| rs373534721 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059691 | TGGTTTTGAAACTAA[A/C]ACTAGATTGGTAGAA | 114792 |
| rs373541055 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066313 | TATGCAGGGGTGTGT[A/G]GGTATACCTAAGCCT | 114792 |
| rs373549652 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003539 | TGTTGCAATTGCTTT[C/T]GGCATCTTTGTCATG | 114792 |
| rs373577142 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010617 | TGAGGAACCACAAAA[A/G]TGTTTTCCTAAAAAA | 114792 |
| rs373582147 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124742 | ATTGTAGGCAAGCTG[G/T]ACGTTAATCTGGTGG | 114792 |
| rs373592590 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050343 | AACAGGATGTGAAAA[A/G]GTTTATTCCTCACAT | 114792 |
| rs373614171 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016285 | TGCAAGCCCATGAAA[A/G]CAGAGAGGGGGACTG | 114792 |
| rs373621810 | in-del | -/TCC | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969402 | ATCCAGTCTTTCCTT[-/TCC]TCATTTTCCTTCTTA | 114792 |
| rs373644934 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050193 | TTTGATTTTTGAAAA[A/G]TGTATTCCTGTTTTC | 114792 |
| rs373645269 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930763 | GGACTCAATGATGTC[C/T]TTTCTCTCTGACAAG | 114792 |
| rs373664125 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950064 | TCAAAGCCAAGATTT[C/T]AAAGTGATATTAATT | 114792 |
| rs373666445 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991668 | CAGCTCTGCCTTAGT[A/G]CCTGATCACTGCGTT | 114792 |
| rs373674040 | in-del | -/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132617 | TATGTAAGAAATGGA[-/T]TTTTTTTTCTTTTTA | 114792 |
| rs373675926 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938687 | GATTTGGAAATAGAC[A/G]GGCCTAAGCTTGAAT | 114792 |
| rs373675949 | snp | A/G | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139148 | AGCAGAGAAGGCAAA[A/G]AAGAAGTATTCTATG | 114792 |
| rs373680196 | in-del | -/GTGT/GTGTGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942654 | TGCTACAGCTGTGGG[-/GTGT/GTGTGT]GTGTGTGTGTGTGTG | 114792 |
| rs373680281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912248 | CCTGGATTTCACCCT[C/T]CTCACTGGCTTTCCT | 114792 |
| rs373716685 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059067 | TGTAGGAGCCAGGAT[A/T]TGAAAGCAGACAGCG | 114792 |
| rs373739395 | in-del | -/TC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111033 | CAGAAAAGTCTTGGG[-/TC]GGGGGGGGGTCTTAG | 114792 |
| rs373766424 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108315 | GAGTTGTGCTTTCTC[A/G]GTGTAATGCCATTAT | 114792 |
| rs373775275 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989059 | TGTATACATATGTAA[C/G]AAACCTGCACGTTGT | 114792 |
| rs373810447 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124755 | TGGACGTTAATCTGG[C/T]GGTTATGGCTCAGAT | 114792 |
| rs373819784 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088244 | CAGCTCAACAATTTG[G/T]TTTTATGTTTCAAGG | 114792 |
| rs373822222 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983517 | TCTGGTGCTGGACTT[C/T]ATTTGGTTGGTAAGC | 114792 |
| rs373896554 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091729 | AATGCTTTGCTTATT[A/G]TTAACTCTCGATAGT | 114792 |
| rs373903507 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103400 | TTGTATTTTTGGTAG[A/C]GATGGGGTTTCACCA | 114792 |
| rs373934279 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025935 | TTGCTATTGTCATTG[A/T]TCTCATTATCACACC | 114792 |
| rs373996278 | in-del | -/C/TC/TTTC/TTTTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135322 | TTTTTTTTTTTTTTT[-/C/TC/TTTC/TTTTC]CCTGAGAGTGTCTTG | 114792 |
| rs374005106 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014380 | TTTGTTTTATAGTAT[A/G]TATAACAAATTGGTA | 114792 |
| rs374019424 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114092 | CGGTACTTCAATCCT[A/G]TTGATCAGGAGAATG | 114792 |
| rs374025294 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104577 | CAGTATATGAGCCTC[A/G]GGCCTCATCAGATTT | 114792 |
| rs374052618 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010867 | AGTTTCACTGAGTAT[G/T]TTGGACAGCATATTA | 114792 |
| rs374059553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984544 | CTAAGGACTTGCTTT[A/G]TGAATCTGGGTGCTC | 114792 |
| rs374068275 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980727 | TAAAAGTAGTTTTAG[C/T]AGGAATTGTACCAGC | 114792 |
| rs374085673 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019514 | AAGGTGTGGGACTTC[C/G]GGTGAAGCACTCACA | 114792 |
| rs374123726 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001265 | GCTGTGCTTGTGGAG[C/G]GGGAAGGAGCTATGT | 114792 |
| rs374140046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130560 | AAATCGCAAAAACAA[C/T]TGGAATATGTGGCTC | 114792 |
| rs374149127 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009488 | CTGTTTTAATTTGCA[A/G]TAGAGCACTTGTATA | 114792 |
| rs374154043 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088548 | GAGTGCAAGAAATGG[G/T]GAGATGTTGGTCAAA | 114792 |
| rs374155228 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998628 | TGTTCAATATTTTCC[C/T]TAGTCAATTTTACAC | 114792 |
| rs374165191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007323 | ATGTAATCCTTAAAG[C/T]GAGCTTTTCAGCTTT | 114792 |
| rs374166407 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106608 | AATAGCTGGGTGGTA[A/G]TGGCGCACGCTTGTA | 114792 |
| rs374172808 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066020 | CCTTTCTTTTCCTCT[C/T]AATATTGTTACGTGG | 114792 |
| rs374184230 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016495 | TCTCACTTTTGGAAC[A/G]AGTGTATTTACCCAA | 114792 |
| rs374229783 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998592 | TTGGTGCATGAATGT[A/C]ACTAAAATTAAATAT | 114792 |
| rs374235205 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046982 | ATAGTATGAAATGTA[C/T]GTATTTTAAGTGTCT | 114792 |
| rs374263353 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946053 | AATGGCTGGGATATA[A/C]GGGTTTACATGAATG | 114792 |
| rs374271414 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929241 | TTTAAAGTTGGAGGG[A/T]TTTTAATTCCTATCA | 114792 |
| rs374277762 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046284 | ACAGGCCCAGGGAAA[C/T]GCAGTGAATTGACTA | 114792 |
| rs374280902 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069400 | GGGTGATTTTGTTCC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs374296916 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946716 | TTGCCATTTTTGCCA[A/G]TCCTGCTCCAACTAG | 114792 |
| rs374302828 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932564 | ACAAAGTTGTCAATT[C/T]CCCCCCCCCCCTTTT | 114792 |
| rs374310426 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952947 | TGTTTACCACAACCC[C/T]GTGAGTTCATCCCCA | 114792 |
| rs374318732 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919747 | AAATAATAAACAGTA[C/G]AGAAAGGTAGAAAAT | 114792 |
| rs374329048 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066031 | CTCTCAATATTGTTA[C/T]GTGGTATAGGAAAGC | 114792 |
| rs374329280 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137481 | CCTTTGTGAAACATG[G/T]ATCCCCAAATTTCAA | 114792 |
| rs374329778 | snp | C/T | 1.64993e-05 | 0.00287218 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064696 | ACAGCTGTTGGAGCT[C/T]CTCAATTTATGCTCC | 114792 |
| rs374348240 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984749 | CCTCCATCCTTTTAT[A/T]TTGAGCCTATGTGTG | 114792 |
| rs374379704 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967747 | TAAGCACACCAGTAA[C/T]GACACAAAAATAATT | 114792 |
| rs374392735 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092675 | TTGGTGCTCCTAGTT[C/G/T]CCAGAGCATATATTT | 114792 |
| rs374394888 | in-del | -/G/GG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111036 | AAAAGTCTTGGGGGG[-/G/GG]GGGGGGTCTTAGCCA | 114792 |
| rs374399634 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933908 | TGGATTGGGAGAGCA[A/G]AAGCAGGTGGAATCA | 114792 |
| rs374444006 | snp | C/G | 3.29603e-05 | 0.00405944 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041512 | GTTCAGTCTTTGTAT[C/G]GTGGAAAGTGGAGCT | 114792 |
| rs374457498 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139591 | GCACTGTCTTAAGAC[-/C]AACATAACACTGTTA | 114792 |
| rs374481821 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935673 | CAGCTGCTGAGTCTA[A/G]TGTGTATTTCTAACT | 114792 |
| rs374498307 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028089 | TCAAGTATGCAAGGA[A/G]TGCTGCAAGGCGGGG | 114792 |
| rs374499123 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917961 | CGTACATTGTAGGAT[C/G]TTTAGCAGCTTCCCT | 114792 |
| rs374534502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036595 | AAATAATCACCTGAG[A/G]TGTGATGATGGGTGG | 114792 |
| rs374556750 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937717 | CTTCCTCCCGTGTCC[A/C]CCTCTACCCTCCATC | 114792 |
| rs374582273 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122575 | ATAGGAACTTGCACT[C/T]AATGGCAGGTTGTTC | 114792 |
| rs374605331 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97041920 | TTATCACTGAAGCTC[A/G]GTGACTCAATCATGG | 114792 |
| rs374614961 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928554 | CTTCTAAAGACTGAA[C/T]ATAAAGTCAAGGGAC | 114792 |
| rs374627603 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966965 | TCTGCATTTAGCTCA[A/G]TGCACCCTTTTCTCT | 114792 |
| rs374627906 | in-del | -/C | 0.434687 | 0.168495 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932565 | CAAAGTTGTCAATTT[-/C]CCCCCCCCCCTTTTT | 114792 |
| rs374631001 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014315 | AAAAAAAAAAAGTTT[C/T]TTTTTTCGTATCTGT | 114792 |
| rs374656737 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132802 | TTCAGCGAGGTTACA[C/T]TTTGCAATGCTGCTA | 114792 |
| rs374664457 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097177 | GAAAAGGAGAGGCAC[A/G]ACTGTTCATTTGCAC | 114792 |
| rs374677672 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014006 | AAGGAAATTTTCTCT[C/G]TGTATATGTTTCTTT | 114792 |
| rs374684905 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097443 | ATGGGCGCTTGCTGG[C/T]TACACTGAGGTAAAT | 114792 |
| rs374690683 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074071 | ACAGTTGAAGGCCTC[G/T]GGTCACACAGTTTGT | 114792 |
| rs374774037 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042822 | GTTTGGATGTTTGTC[C/T]TCTCCAAATCTCATG | 114792 |
| rs374782237 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104952 | TAGTATACACTTTTC[A/T]CTCTATGGCAGTTGC | 114792 |
| rs374812041 | in-del | -/AGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964175 | TTCTGGATTCTGAGG[-/AGG]GGAACTGCAGGAGAC | 114792 |
| rs374842891 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066057 | AAAGCTATTTTTAAT[C/T]CCTTTCTGCCTGTAG | 114792 |
| rs374861096 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101636 | TTCATTCATGCATTC[A/G]TTCATGCTTCTCCAA | 114792 |
| rs374864074 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903125 | AAACAAACAACAAAA[A/C]AAAACAGTTGGTTCC | 114792 |
| rs374867944 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976454 | AAATGTGGCACTGTA[G/T]TGCTTCATGTGGGGG | 114792 |
| rs374870998 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132328 | TCTATAATATACCTT[A/G]TTTCCACCACTGTAA | 114792 |
| rs374872641 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038972 | GCACGTGCCTGTAGC[C/T]CCAGCTACTCAGGAG | 114792 |
| rs374877748 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934425 | TCTGGATCTGGGCCT[A/C]AGCTTTCTTGTCATT | 114792 |
| rs374882820 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924634 | TGGCGTCTGAACCCG[C/T]CCCGGGGGTGCCAAG | 114792 |
| rs374884147 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917187 | AAATGAGAAATTTAT[C/T]GCAAACAAAATTAAA | 114792 |
| rs374891187 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897036 | GGTTCGAGAGATTCT[C/T]CCACCTCAGCCTCCC | 114792 |
| rs374895219 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042279 | GTCTTCTCTTGAGAT[A/G]CTCACATCCTAGTAA | 114792 |
| rs374912432 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098320 | TCATCATATATTAGG[C/T]ACCTGAGAGCTAGAA | 114792 |
| rs374968096 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927210 | TCCTGGCTTAATGTT[G/T]TTTTTCTTGCCATAA | 114792 |
| rs375006800 | snp | C/G | 1.69372e-05 | 0.00291004 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132606 | GGTTAATTAAAATAT[C/G]TAAGAAATGGATTTT | 114792 |
| rs375021928 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061612 | TATCTGTCCTGGTTT[A/G]AGTGTCAGACTACAT | 114792 |
| rs375039277 | snp | A/C/G | 6.62113e-05 | 0.00575342 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132780 | CTTTTGAAGTTTGTT[A/C/G]AAGTGGTTCAGCGAG | 114792 |
| rs375051680 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135791 | CATTTTTTTATGTTA[C/T]GGATGACGATAGAAC | 114792 |
| rs375082400 | snp | C/T | 9.93213e-05 | 0.00704633 | intron-variant, synonymous-codon, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114523 | AGGTAGAACATACCT[C/T]ATGTTGGATTTATCA | 114792 |
| rs375095601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959109 | CTAGAGAAAGATGAG[C/T]GCTGATTGGAAAATT | 114792 |
| rs375106802 | snp | A/C/G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989718 | TGCTTTTTCTCCCCC[A/C/G/T]CTCTCTTCCAGGGAT | 114792 |
| rs375109580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925794 | GCATCAGTATTGAAG[C/T]GCAGTTTTTTGCACC | 114792 |
| rs375120793 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102914 | ATGTCATGGGGGTTT[A/G]TACAGATTATTTCAT | 114792 |
| rs375137363 | snp | A/G | 1.65952e-05 | 0.00288051 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132793 | TTCAAGTGGTTCAGC[A/G]AGGTTACATTTTGCA | 114792 |
| rs375169535 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981487 | TTTATCTTATTTATT[A/C]TTTTGAAGAACAAAC | 114792 |
| rs375178231 | snp | C/T | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085199 | CTTTGTTGGAGAAGG[C/T]AGTGATCGATTTCTT | 114792 |
| rs375184756 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931092 | TTTATGAAAAGGTCA[A/G]AAGCTCACCAGGATA | 114792 |
| rs375190143 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912991 | CTCGCAATTTTTTGT[C/T]GTCTGAATGAATATA | 114792 |
| rs375195143 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051718 | CTTCCTTTAGGTGCT[C/T]CCTCAAATCATCTTA | 114792 |
| rs375195164 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972587 | GCTTCTGTGGGAGAC[C/T]TTTTCCAGTTTTAGG | 114792 |
| rs375205586 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089779 | AATGAAACTCCAGCT[A/T]AAAAAAAAAAAAAAA | 114792 |
| rs375213187 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038004 | CCCTTATCTCTCACC[A/G]TACACAAAAATCAGA | 114792 |
| rs375216505 | snp | A/G | 4.94352e-05 | 0.00497143 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139188 | TCCCTTTTGCTTCCA[A/G]TGGAATAGCAGCATG | 114792 |
| rs375223463 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049048 | AAATCCACATTTTAA[G/T]GAAGAATATAGCATC | 114792 |
| rs375233555 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940341 | TGATTAGGTAGAGAG[A/G]GATAAGCAAAAAGGA | 114792 |
| rs375261819 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065590 | GTGTCACCTTCACTT[A/G]CATTTATTATAGCAT | 114792 |
| rs375287493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975424 | AAGTTTAATAATAAG[C/T]TTCTCTGGTTTAATT | 114792 |
| rs375303089 | in-del | -/AATT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904584 | TTCAAAAAATTAATT[-/AATT]TGATACACTTTCAAT | 114792 |
| rs375308977 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094767 | TACAAGTCAGTATTG[A/G]TAAGTGGCACGGTAT | 114792 |
| rs375344133 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060004 | TGCAGTTGTACAAGC[A/G]CTTGTTTTGCTTGCA | 114792 |
| rs375360082 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013117 | TACATAAGTGAAATA[C/T]AGTAAATGCTCTTAA | 114792 |
| rs375374140 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056788 | TCACGACCATAGTCT[C/T]AGCACTTTGGGAGGC | 114792 |
| rs375387513 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079621 | ACTTGAAAAACTGGT[A/G]TTTATTCCATAGCTA | 114792 |
| rs375399576 | in-del | -/AG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916368 | AAATATAGAAGTACA[-/AG]GTCTTTCTCAGGACA | 114792 |
| rs375400107 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017193 | AAAAAAGAAAAAAAA[-/A]TCCTGGACACATCTG | 114792 |
| rs375400415 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016443 | TTGTTGGATTTCAGA[C/T]TTGCATGGAACTGTA | 114792 |
| rs375406233 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134237 | AAAATTAATAAACTG[A/G]GAAACAATAATACAG | 114792 |
| rs375411815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915407 | ATGAAAGACACTGAC[A/G]TATGAACAAAAAATT | 114792 |
| rs375413264 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992238 | ATGGCTCCCGGGACC[A/C]AGGGTTGCAAAGGTC | 114792 |
| rs375414969 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056167 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 114792 |
| rs375432969 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962279 | GACCCCATCAATCCT[A/G]TGTACCAGATTATAT | 114792 |
| rs375475670 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970161 | CCCAACTCCATCATT[C/G]AGCTGAACCACAGCC | 114792 |
| rs375479823 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087819 | TCTGGCTCTGAAGAC[A/C]TGTCATAAGAACCTT | 114792 |
| rs375488608 | snp | A/G/T | 0.000135046 | 0.00821613 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139307 | CCATCATGAACAGGA[A/G/T]GAAAACATAGCTCTG | 114792 |
| rs375582825 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977326 | TAAATGGCAGATCTG[G/T]AATCGAAATCTATGT | 114792 |
| rs375586519 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011654 | TCAGAGTGATCATTT[A/T]TCTTGAATTAAAATT | 114792 |
| rs375588669 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985937 | GTGTCCTTTGGAGGA[A/G]GAGAGGTGCTCTGAT | 114792 |
| rs375591256 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923649 | TGAGAACATTAAGGA[C/T]ACCTCAAAATAGATC | 114792 |
| rs375595740 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975559 | GGTACAAAGGTGGGG[A/G]AGGAATCAGGGAATT | 114792 |
| rs375602476 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916998 | CCCTGAACCCTTTCT[A/G]GAGTCAAAAACATAA | 114792 |
| rs375610104 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078801 | CACTGTAGACTAACT[C/T]CATTATCTACCCCAC | 114792 |
| rs375641003 | snp | A/G | 1.74366e-05 | 0.00295263 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085079 | CCTGCTCTTTCTCGG[A/G]TTTATTTCTAAGAGA | 114792 |
| rs375653602 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951735 | ACCTTGTGAGATAAG[A/T]TTTATATATTTTTTA | 114792 |
| rs375697057 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004518 | CCAGTGCTGTGTTGA[A/G]TAGGAGTGGTGAGAG | 114792 |
| rs375723833 | snp | A/G | 3.33428e-05 | 0.00408293 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041614 | GGTATGGTATTAAAT[A/G]TGATCTGTAAAGTTT | 114792 |
| rs375749272 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099974 | ACATGGTGAGATCCC[A/T]TCTCTACTAAAAATA | 114792 |
| rs375801712 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950982 | AAGCCTTGTAATACA[A/G]ATTACTCAGTTTGAA | 114792 |
| rs375808864 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112410 | CTAATTAAATTACTT[C/T]AGGTGCTCCATAAAT | 114792 |
| rs375829787 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960811 | CAGCTGGAAGCGGGG[-/G]CTTCTGGGTCATAGG | 114792 |
| rs375853506 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028240 | TTCTTACAAGTTCCT[C/T]GGCAATACCAATGCT | 114792 |
| rs375854662 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036967 | TGTTGGCACTAAGCT[A/G]TACTATGTGGAACAT | 114792 |
| rs375902804 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076579 | CCAGTGCCTTGTTCC[C/T]GCAGTTTACCACCCA | 114792 |
| rs375915997 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135295 | AGCACAGACAAATTT[G/T]TTAATTTTTTTTTTT | 114792 |
| rs375925484 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043353 | CTTATTTCACTTAAC[A/G]TAATGTCCTCAAAGT | 114792 |
| rs375947129 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998029 | AAGGATAAATGGCAG[C/T]ATAACATTGACAGTA | 114792 |
| rs375968485 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012189 | ATAATAGACCCCCTG[G/T]CCAAAGATGTCCATG | 114792 |
| rs375991795 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056231 | CTGCCTCAGCCTCCC[G/T]AGTAGCTGGGACTAC | 114792 |
| rs376057056 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072577 | GGCTTTTTTTTTTTT[G/T]ACAATTTACTACCCA | 114792 |
| rs376058389 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009334 | TAAATTTAAATGTTT[A/C]TTTTATTTTGAAATA | 114792 |
| rs376082192 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062941 | ATCTGAAGTATATGA[A/G]GGAGTGGCCCAGGCA | 114792 |
| rs376084282 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983113 | GAATTTTCTCAAAGG[C/T]CTTTTCTGCATCTAT | 114792 |
| rs376093036 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096436 | AAGTAGAAGCTTATT[C/T]TCACCACTCCAAGCG | 114792 |
| rs376094567 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064105 | AAAGAGGAAAATGGA[A/T]GTTTGCGTATGAAGC | 114792 |
| rs376110357 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055622 | GGCCAACATGGTGAA[A/T]CTCTGTCTCTACTAA | 114792 |
| rs376138032 | snp | A/G | 3.40791e-05 | 0.00412776 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976144 | ATTCCATGCTCACAA[A/G]GCAGTCCTAGCAGCA | 114792 |
| rs376156341 | in-del | -/TTTTTTTTT | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118634 | TTTTGTCTACAATTC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 114792 |
| rs376170680 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074341 | GAACTCCCGCTCTAG[A/T]TTCTGTTGCCACACT | 114792 |
| rs376184475 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984968 | GTTTCTTCCTAGCCT[C/T]GATGGTCTTTACAAT | 114792 |
| rs376209929 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055802 | AACCTGTCTAAAAAA[-/C]AAAAAAAAAAAAAAA | 114792 |
| rs376218122 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969542 | ATATTTCCATGCCTA[C/T]GTTGTCTAGTGGAGA | 114792 |
| rs376256165 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045964 | ATGAAAATATATCTG[A/G]TGTAAGTGCCTTTAA | 114792 |
| rs376267501 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058157 | AACTGTAGTTTTTTT[-/TA]GTCTTGAAGCGGGTA | 114792 |
| rs376298307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901977 | CATTTTATCCAGTCT[A/G]TCATTGATGGACAGT | 114792 |
| rs376334939 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938835 | ATGCAGTGATGTATG[C/T]AAGTTTCATTGTCTA | 114792 |
| rs376362346 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097129 | GGAGGGAAAAAAACC[A/T]CGCAAATTTAAGAGT | 114792 |
| rs376369213 | in-del | -/A | 0.499923 | 0.00618962 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985745 | TTTAAGGACTTCTCT[-/A]GAATTGGTTATTCTA | 114792 |
| rs376380805 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949184 | AATAGGGACATTGCA[C/T]GTCTTGTTTTAAACT | 114792 |
| rs376388348 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042023 | CCTCCACATATCTCA[C/G]AGTCAGAATTGAAGG | 114792 |
| rs376451165 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050534 | TTAAACCTTTGCTCA[C/G]ATGTAAGGCAAGCAG | 114792 |
| rs376452776 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973999 | AGTACTGGGATTACA[A/G]GCATGAGCCACCGTA | 114792 |
| rs376467895 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072993 | GTCTACCTTTTAGGG[A/G]TGTTGAAGGATTCAA | 114792 |
| rs376478210 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930667 | ACCTTGGAGCAGAGC[C/T]ACCCTCATTATGCTA | 114792 |
| rs376529786 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937232 | CATTTGCAGTTATTC[A/G]CCACCCCCTCTCCAT | 114792 |
| rs376553787 | snp | A/G | 0.000230643 | 0.0107363 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113842 | GGACGAGCTCCTGCA[A/G]TACATCCGCTTTGGC | 114792 |
| rs376569304 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965743 | AAACAACGTGCCTTG[A/G]ATTATTCTGACTGCC | 114792 |
| rs376571420 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900995 | CTGTAAAACCTAGAA[C/T]ACTGGGAGCGGGGGG | 114792 |
| rs376578407 | snp | G/T | 0.000183819 | 0.00958518 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967013 | GGAATGCTTGCTGAT[G/T]CCTCTGCACACTTCT | 114792 |
| rs376582170 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947635 | AGTACAGATGGGAAG[A/G/T]TATATTGCCTTTTGT | 114792 |
| rs376591889 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958423 | ACCAGGCAAAAAGGA[A/G]GGGTAGAAAGTTCTA | 114792 |
| rs376620209 | snp | A/T | 3.70927e-05 | 0.00430639 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975972 | GGAAAAGGAAAAATG[A/T]TGACTTGATTGCTCT | 114792 |
| rs376658867 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948958 | AACTTTCTTATCTCC[A/G]ACTTTAGAATCTTTT | 114792 |
| rs376665248 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992472 | CTCTCTTCTCTCTCT[C/G]AGAGCAATGCGCACT | 114792 |
| rs376680370 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899398 | ATCATGGTAGCAATT[C/T]GACTCACTGCCTGTT | 114792 |
| rs376709728 | snp | C/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111033 | ACAGAAAAGTCTTGG[C/G/T]GGGGGGGGGTCTTAG | 114792 |
| rs376715196 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055829 | AAAAAAAAACCCCTT[C/T]TTATTTCTATATTCC | 114792 |
| rs376715430 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010544 | TATATATCATCTTGT[G/T]ATTTTAGATATTGAA | 114792 |
| rs376730375 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140701 | TTGTTATTTTATTCA[C/T]GTAACCTTTTTTTGT | 114792 |
| rs376747531 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121806 | TATGTGAACAATATC[A/T]TTTGCTTTATTCCCA | 114792 |
| rs376778001 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011719 | TATGGACATGCTGAC[A/G]TAAAAGTATTTAAAA | 114792 |
| rs376799708 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937714 | CCACTTCCTCCCGTG[C/T]CCCCCTCTACCCTCC | 114792 |
| rs376801343 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122849 | GTAGGACCCATGTTA[A/G]TGCCACAGCCTGTCC | 114792 |
| rs376810099 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919906 | AACTAAGTAGGCATT[C/T]TATAAAACTTGCCTC | 114792 |
| rs376825964 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958748 | ATGTTTCCCCACCCA[A/T]TGGAAAGAATTCAGA | 114792 |
| rs376830548 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115432 | AGTTTGAGCTCTAGT[A/T]TACCTTTTCATCTCT | 114792 |
| rs376842514 | snp | A/G | 3.30486e-05 | 0.00406487 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139255 | TCAAACTCTTCAAGT[A/G]CCTCATCACAGGATT | 114792 |
| rs376847257 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056531 | CTCCCCACTCTGTAG[G/T]CTTCAAATCCTTCCT | 114792 |
| rs376895166 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982299 | GACCCTTTACCATTA[C/G]GTAATGCCCTTCTTT | 114792 |
| rs376896905 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988693 | ACAATAGCAAAGACT[C/T]GGAACCAACCCAAAT | 114792 |
| rs376901209 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114190 | TGTGGCAGTCATGGG[A/G]GACTTCCTGTTTGTG | 114792 |
| rs376908118 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048631 | CCCTGATAATGCAAA[C/T]ACTGTGCATTACATT | 114792 |
| rs376919736 | in-del | -/AAAC | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138578 | CCCCAAAAACAAACA[-/AAAC]AAACAAAAAAACTCC | 114792 |
| rs376941896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029173 | CAGAAGACCCAGGTC[A/G]TTGAAACATGGCCAC | 114792 |
| rs376943897 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097464 | TGAGGTAAATGAGAA[C/T]GTGCAGTCTTGGATA | 114792 |
| rs376955043 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015742 | TAATTGCCAAGACCA[G/T]GGGGAAAATGTCCCC | 114792 |
| rs376956855 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902861 | CCTTTCCCCCATTGC[C/T]TGTTTTTGTCAGGTT | 114792 |
| rs376963868 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908363 | AAGAATAAACGTATA[C/T]TTGTAATGATAAAAC | 114792 |
| rs376966371 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101478 | AATCTTTCTCACCAA[-/G]TTTCTGACATATAAT | 114792 |
| rs376966964 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103455 | CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC | 114792 |
| rs377000276 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015741 | TTAATTGCCAAGACC[A/G]TGGGGAAAATGTCCC | 114792 |
| rs377025227 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978797 | TTCTCTGCAACCTCT[C/T]CATCATCTGCTATTT | 114792 |
| rs377051017 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915326 | GCATGGTAAAAGGCA[C/T]AAAAAAAGATAAGAC | 114792 |
| rs377070555 | in-del | -/TACACATA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943120 | ACACATATACACATA[-/TACACATA]CCAGCATATAGACAC | 114792 |
| rs377094706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964717 | TTAATTCAATATATA[C/T]ATTTTAATCAAGTAT | 114792 |
| rs377097701 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034567 | CACTTGAATTTTGAT[A/G]GGGGTTGTGTTGAAT | 114792 |
| rs377105134 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055868 | TACCACTTATTTCTC[C/T]GACTCTTCTCACAGC | 114792 |
| rs377106973 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020805 | CAGGTTTTCCTCCCA[C/T]TTGCTGGCTGCCCCT | 114792 |
| rs377115721 | in-del | -/TTTT | 0.498908 | 0.0233371 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100967 | CCACTGCAGCCAAGC[-/TTTT]TTTTTTTTTTTTTTT | 114792 |
| rs377133164 | in-del | -/ATATTTACTGTAAGAAAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907065 | ATAAGTGGTCTTAAT[-/ATATTTACTGTAAGAAAT]TATAAGTATTTATGC | 114792 |
| rs377137985 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985183 | ATTCTTTTCTTTAAG[A/T]ATGTTGAATATTGGC | 114792 |
| rs377175499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127306 | TACAAACAGATCCTC[A/G]GCAGTAGCTAATTCT | 114792 |
| rs377177549 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094599 | CTCCTTGTTACGTGC[A/G]GTGGCATGTTGATGA | 114792 |
| rs377182082 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090065 | GGGCTGGGGCAATCC[C/T]GTTCATATTTGTCCG | 114792 |
| rs377204330 | in-del | -/CCCCCC | | | cds-indel, intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113808 | GTGGTTGGAACACAA[-/CCCCCC]CTGCCACTACCAGTA | 114792 |
| rs377225947 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025411 | AAATCATTCATATCA[C/G]TTTATAATCACAATA | 114792 |
| rs377231884 | in-del | -/GTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115333 | AAACAAAGTTTGTTT[-/GTTT]TTAATTATCCGTGAA | 114792 |
| rs377250179 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920982 | TTGACAAGTTGTTTT[C/G]CAAAATATTTTTTTG | 114792 |
| rs377252298 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914369 | CTTGCTTAACTTTGA[A/C]TTTTTATCTAGTGGG | 114792 |
| rs377280621 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998524 | GGTTACTGTAAGCAT[A/G]TAAATATTTACTACT | 114792 |
| rs377284917 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990698 | GAGAAATACGGAGCT[G/T]CTACCAGTTGGTGTG | 114792 |
| rs377339491 | snp | C/G | 5.13466e-05 | 0.00506662 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139326 | AACATAGCTCTGACT[C/G]TTGGATACTGGGCAT | 114792 |
| rs377352668 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913821 | TGGCACTGTCCCCTC[C/T]GTCATGGGGGAAGGG | 114792 |
| rs377367474 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043319 | TGAGATCATGAAGTA[G/T]TTGTCTTTCTGTGCC | 114792 |
| rs377374768 | snp | C/T | 0.000153988 | 0.00877328 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896758 | CCTGCAAGGAAGACA[C/T]AGGATCTTTGGAATC | 114792 |
| rs377376647 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107171 | GGTGGCAGGTGCCTG[C/T]AGTCCCAGCTACTCG | 114792 |
| rs377379951 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928549 | TGATTCTTCTAAAGA[C/T]TGAACATAAAGTCAA | 114792 |
| rs377441057 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942005 | AAAAAGACTGGCATA[G/T]GTACTGTATATATAG | 114792 |
| rs377442471 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018425 | ACCCTGTCTCTACTT[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs377451940 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911608 | CTTATTTCCACTTCC[C/T]GCCTCCCATTTACTC | 114792 |
| rs377475300 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983718 | TATTTCTGTGGGATC[A/G]GTGGTGATATCCCTT | 114792 |
| rs377493228 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010358 | CAGGACTTGTTCATA[C/T]GTCTGTCTCTCCCTC | 114792 |
| rs377498557 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079024 | GAGCGTGACATCCCT[A/G]AGCTAGGCTGTGGGT | 114792 |
| rs377500380 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906430 | CAGGTGGTGGTAGAG[G/T]TTTAAAATGATCGGA | 114792 |
| rs377515152 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118501 | GCGGGCGCCTGTAAT[A/C/T]GCAGCTACTTGGGAG | 114792 |
| rs377531798 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030466 | TGGATTATATACTCA[A/C]AAACTAGGTTTTCAA | 114792 |
| rs377534743 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999893 | TTTGTGCCGGATGTT[A/G]CAAGGGCTCCTAAAA | 114792 |
| rs377553815 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014832 | CTCCTACTCTGCTGA[A/G]TAGCTTAGTATGAGA | 114792 |
| rs377567832 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136790 | TTCCTTTTCCCTTCT[C/T]AGATTAAATACATTA | 114792 |
| rs377571329 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074696 | GGCTAATTTTCAGCA[A/G]TCTGACTTTGTGTAC | 114792 |
| rs377583802 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916880 | TCATCATAAAGGAAC[C/T]GTTTTTCCATCTAAA | 114792 |
| rs377607417 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036917 | TCCTCCTGCTCTTTT[C/G]CCCTATGGGGGGATA | 114792 |
| rs377610672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022970 | ACAAGGTGGTAGGAG[C/T]GAGAAGAGAGCAGGG | 114792 |
| rs377611033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049588 | GTCGATAACGGGGGG[C/T]GGGGGGGAACTACTT | 114792 |
| rs377611651 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953290 | ATGTTGCCAGTCTTG[A/G]TTTTTGATGTTTGAG | 114792 |
| rs377613410 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935598 | TAGTATTGGGCCATC[C/G]AGCCAAAATTATCTT | 114792 |
| rs377618096 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928245 | GAACTTGATGGCTGG[A/G]TATGATTATATTAAA | 114792 |
| rs377628529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058671 | TTGTTTTTCTGATAA[A/T]CAATGCCAGACTCAG | 114792 |
| rs377661836 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026903 | GCGTAGTGGCTTACA[C/G]CTGTATTCCCAGCAC | 114792 |
| rs377691285 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040206 | CTGCAGAATCTCAGG[C/G]AACAGTTCCCACAAA | 114792 |
| rs377717365 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021768 | ACAGCCTGCTTATCA[A/T]CTCTAGTTGGATGTT | 114792 |
| rs377718284 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115988 | AAATTCATTTGGACT[C/T]TGACTGTTCTTCTGC | 114792 |
| rs377718400 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980001 | CTACTGATATTCGTA[A/C]AATTGATTTTGTATC | 114792 |
| rs377719097 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013904 | GCTCATTTTATAAAT[G/T]TGTTGTCCTAAAGTT | 114792 |
| rs377720610 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019195 | TATTTAAAACTGAAT[A/G]CCAGAAAAAAGCAGC | 114792 |
| rs377725302 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028587 | GCAGACTCTAATCAC[A/C]ACTGCTCAGTCATTC | 114792 |
| rs377725857 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947075 | AGGCCATTAGGCTGA[G/T]ACGGCTCCAGCACCT | 114792 |
| rs377726046 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932727 | GTGTATCACCACACC[C/T]AGCTAATTTTTAAAA | 114792 |
| rs386704078 | multinucleotide-polymorphism | CGC/TGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901379 | CTTCTAGAGACTTCC[CGC/TGA]ATTTCTTGGCAGCCA | 114792 |
| rs386704079 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940680 | GAACAGATAATAAGC[CA/TG]AGTTACAGAAAACAG | 114792 |
| rs386704080 | multinucleotide-polymorphism | AT/GC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956991 | TCAATAGAAGAAAAT[AT/GC]AGAATGTCTTATACT | 114792 |
| rs386704081 | multinucleotide-polymorphism | AGT/GGC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982227 | CTGTTTATTAATCTG[AGT/GGC]GCTCCTGTGTTGCGT | 114792 |
| rs386704082 | multinucleotide-polymorphism | AG/GC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992336 | CTCCCCTGGCTCTTC[AG/GC]CTCTCCCCGGTGGGC | 114792 |
| rs386704083 | multinucleotide-polymorphism | AA/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003692 | AGGAAGGGGTCTAGT[AA/TT]CAAAGTTCTGCATAT | 114792 |
| rs386704084 | multinucleotide-polymorphism | CA/TG | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008778 | CCTTTCCCTCCAGCC[CA/TG]GCCTCTATGTCTTCC | 114792 |
| rs386704085 | multinucleotide-polymorphism | CA/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022658 | TATTTTTAGTAGAGA[CA/TG]GGGTTTCATCATGTT | 114792 |
| rs386704086 | multinucleotide-polymorphism | CCG/TCA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022668 | AGAGATGGGGTTTCA[CCG/TCA]TGTTGGCCAGGCTGG | 114792 |
| rs386704087 | in-del | C/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029494 | ATAATTTTACTGTTT[C/TA]GTTTGTCTTGTGATA | 114792 |
| rs386704088 | in-del | CCTATTA/TAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031947 | TAGCGACAGTTTCTA[CCTATTA/TAT]AACATTTACTATGTG | 114792 |
| rs386704089 | multinucleotide-polymorphism | AC/GT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036276 | TTTTGTTTATGTATT[AC/GT]TTTCCTGATATTATT | 114792 |
| rs386704090 | multinucleotide-polymorphism | AC/GT | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040800 | GCTGTTCTCATGATA[AC/GT]GAGTGAGTTCTCACA | 114792 |
| rs386704091 | in-del | C/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132888 | AACTAGTTCAGCCAC[C/TA]AACTTCATCCTGTAT | 114792 |
| rs386704092 | in-del | A/TATAT | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139651 | CGATGATCTTAAAAA[A/TATAT]ATATTCTGTACTTAA | 114792 |
| rs397757577 | in-del | -/A | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994756 | TAATGCTTTAAAAAA[-/A]TAACAAAAATGTTAG | 114792 |
| rs397785520 | in-del | -/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901342 | CCTTTTTTTTTTTTT[-/T]ACTTTAAATGGGGAA | 114792 |
| rs397788272 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961627 | CTCAGATCTACCTCT[-/CT]GAAAATAGGGCTTGG | 114792 |
| rs397792679 | in-del | -/TGTT | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115996 | TGGACTTTGACTGTT[-/TGTT]CTTCTGCTGTCCTCA | 114792 |
| rs397796019 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950241 | TGTTAAAAAAAAAAA[-/A]CCATTAGCTCTCTAA | 114792 |
| rs397809830 | in-del | -/A | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083405 | AAAAAAAAAAAAAAA[-/A]TTGTACTTGGGGAAT | 114792 |
| rs397820937 | in-del | -/A | 0.375 | 0.216506 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097643 | TCCATTTGAAAAAAG[-/A]AAAAAAAAAGGCAGA | 114792 |
| rs397824067 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950240 | GTGTTAAAAAAAAAA[-/A]ACCATTAGCTCTCTA | 114792 |
| rs397835584 | in-del | -/ACACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943065 | cacacacacacacac[-/ACACAC]tctgtacatacacac | 114792 |
| rs397885690 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991596 | TGGAGAGATCCTGCC[-/C]ATTGAGGGGTAGCAG | 114792 |
| rs397886156 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922517 | CTTTAAAAAAAAAAA[-/A]TCTTCTTCAGCTCAT | 114792 |
| rs397886235 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104356 | AGTTGCAAGGGCTTT[-/T]CGCTTTTGGAACTCT | 114792 |
| rs397886731 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105123 | AATATTAAAAGGATA[-/A]CATGCTAAAGTTTTA | 114792 |
| rs397888404 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065994 | TTAATGATTTTTTTT[-/T]ACCTTATTTTCCTTT | 114792 |
| rs397960115 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941756 | ATAGCTGCCTTTTTT[-/T]CTCTGATTTGTCCTT | 114792 |
| rs398002379 | in-del | -/GT | 0 | 0 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924835 | TTTGTGTGTGCGAAA[-/GT]GTGTGTGTGTGTGTG | 114792 |
| rs398002380 | in-del | -/A | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953867 | TATAAAAACATAAGC[-/A]AAAAAAAAAAAAGAC | 114792 |
| rs398002381 | in-del | -/A | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954333 | GAGAATTATCTAAGC[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs398002383 | in-del | -/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027177 | TCCCTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs398048687 | in-del | -/AAAC | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931122 | AAAAAACAAACAAAC[-/AAAC]AAAAAACACTCCTCA | 114792 |
| rs398048688 | in-del | -/TAGT | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949329 | CTCTGATATTCTAGT[-/TAGT]CAGTTTTCTCTTCAT | 114792 |
| rs398048689 | in-del | -/A | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953328 | GTTTCCCATGAAAAA[-/A]GATGAAAATTTAGGT | 114792 |
| rs398048690 | in-del | -/T | 0.5 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971038 | TGTTAGATTTTTTTT[-/T]GTCCAGCCTTTTTCT | 114792 |
| rs398085155 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922516 | ACTTTAAAAAAAAAA[-/A]ATCTTCTTCAGCTCA | 114792 |
| rs398085156 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931887 | ATCATTATGAAAAAA[-/A]AGCCTACTCTAAATG | 114792 |
| rs398094416 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007261 | TCGAGTTCTGAGACT[-/CT]TTCTTTGGCTTCATC | 114792 |
| rs398110451 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989719 | CTTTTTCTCCCCCCC[-/C]TCTCTTCCAGGGATA | 114792 |
| rs527260461 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913255 | AATTCTGCATATCCT[A/G]TTTGAGAGCAGAAGC | 114792 |
| rs527282659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029805 | CCAAAATGTAATAAA[A/G]GCTAATAACCATTAA | 114792 |
| rs527294932 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915496 | GAAGGAATAGTGTGG[C/T]TGTCTTCTTTGTGAT | 114792 |
| rs527300267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070670 | CTCTTGAAAGAGTTC[A/G]CTAATAATATTAGTC | 114792 |
| rs527302993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989390 | ATGAATTTCTTGGAT[A/G]GAATTTTTTTCTTTA | 114792 |
| rs527307905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078526 | TCCTATTCAATTTGG[A/G]CATCTTAGAGGGGGA | 114792 |
| rs527317968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941961 | ATGCAAAATGCATGT[A/G]TGAATATGGTCTCAG | 114792 |
| rs527318271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022396 | TTCCTTCCTTGCCCT[C/T]TGCAGGTCTTTGCTC | 114792 |
| rs527333799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934907 | AGTATGGATATAGCA[C/T]GATATGAGGAGCAGA | 114792 |
| rs527334388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979768 | TATGGCCATTTTCAC[A/G]ACATTGATTCTTCCT | 114792 |
| rs527345590 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073529 | AACATCTTTCTCCAT[C/T]CTGGTATACAGAATC | 114792 |
| rs527359716 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928359 | ATACCTAATATTGAT[G/T]AGCTTACTGTAGCTG | 114792 |
| rs527382244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071218 | TCAGTGTTCTGCCTT[C/T]ATTACTCCTCAAAAG | 114792 |
| rs527395271 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028247 | AAGTTCCTTGGCAAT[A/G]CCAATGCTGCTATTC | 114792 |
| rs527398263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016084 | GCTGCAGGGTTGGAG[C/T]CCTCATGGAGAACCT | 114792 |
| rs527405616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023089 | ATCACCTCCCACCAG[G/T]TCTCTCCCTTGACAT | 114792 |
| rs527410465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113428 | GACATTTCCTGGTGG[A/T]GGGGTGTACTGAGCC | 114792 |
| rs527419138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972095 | GACCTCAGATGATCC[A/G]CCCACTTTGGCCTCC | 114792 |
| rs527424182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980374 | TTTTAACATGAAGGG[A/C]AGTTGATTTTTATCA | 114792 |
| rs527438875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064335 | GGGTTATGTTTTTCT[C/T]TGAAAATGTTTATAC | 114792 |
| rs527455672 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030374 | TTTTAGGACTCAATT[A/T]GCATCACTTCTGTGT | 114792 |
| rs527471950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928878 | TTTAAGGTTGCATAT[A/G]CTTTTGATGAAGTCT | 114792 |
| rs527475398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973230 | AAAGCTGAGGCTTTT[A/G]TTCTTTGCCAAATTT | 114792 |
| rs527483357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003051 | TCAAATGGTAGTTCT[A/G]AGTTCTTTGAGAAAT | 114792 |
| rs527488812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064978 | CGACCATTGAGCAGC[C/T]GATCAACTCAGTGAC | 114792 |
| rs527524077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107627 | AAATAGAAGTGGCCA[A/G]CACCAAACATGTGAG | 114792 |
| rs527525814 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054270 | TATTGAATACTCTAA[A/G]TTAACTTGTGAATAT | 114792 |
| rs527540403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009338 | TTTAAATGTTTCTTT[C/T]ATTTTGAAATAATTT | 114792 |
| rs527545196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922485 | AGAGAGTTTTCAGTT[A/G]CAACCAAAGACTCAC | 114792 |
| rs527549933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970880 | GGGTCTTTTAATATC[A/C]TGCTACCTTAAATAT | 114792 |
| rs527550555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974082 | TATATTCTTGGTGAT[A/C]GGTTCTCAAAATACC | 114792 |
| rs527550719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058508 | TCATTTCCTCTTTTT[C/T]CTTTATATAGAACTC | 114792 |
| rs527552829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051462 | CAGTAACTCCAAACA[A/G]TAGATCAACCCTCCT | 114792 |
| rs527568113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009739 | CCTGTATTTCATGCT[C/T]ATACCTACTAAAGCA | 114792 |
| rs527588989 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966706 | AATTTCTTTCCTTTG[C/G]CCATTCCATCTCTTG | 114792 |
| rs527590912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092710 | TTTCCTTCTAATCTA[C/T]ATGCGGCTAACTCCT | 114792 |
| rs527617582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044339 | TCATTGCATCCCAGG[G/T]ATAAATCTCCCTTGA | 114792 |
| rs527653608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093546 | GTCAAACGTTTTTAT[A/G]TATTACTCTGTAATG | 114792 |
| rs527659864 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023584 | AATCCAGGGCAACAA[A/C/G]GATTGTACCCATTCC | 114792 |
| rs527660244 | snp | G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995810 | AAGTTCATATGTAAG[G/T]TTCCCCTTTTTTGAA | 114792 |
| rs527663169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906196 | ATGACCCTAAACAGG[C/G]AACCCAGTTAAGCCT | 114792 |
| rs527714772 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094388 | CTTAGAAGTGCTTCT[C/G]CCACCCTTGCCTCCA | 114792 |
| rs527719510 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025255 | TGGGATGATCCAGCT[A/G]CTTGTTGAATCGGTT | 114792 |
| rs527724939 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906937 | AGTCTCCAGAGAAGG[C/T]TAAAAATATGACGTC | 114792 |
| rs527736777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045520 | AAGTAAATAATATCT[G/T]CACTCAGCTGCATTA | 114792 |
| rs527747689 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129647 | AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA | 114792 |
| rs527748303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138452 | GGTGAGGCAGGAGGA[A/T]TGCTTGAGCCCAAGA | 114792 |
| rs527777967 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003807 | GATGGTTGTAGGTAT[A/G]TGGCTTTATTTCTGG | 114792 |
| rs527781697 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087077 | AAAGGTTACTAATAT[C/T]ATAATGTAGAATTTT | 114792 |
| rs527784016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997031 | GGATGGCGATGGGGA[A/G]GAAAGACAAGAGTGA | 114792 |
| rs527790782 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031201 | CCTTATCACCAAGTG[G/T]TATCCAATGAGGCTC | 114792 |
| rs527798002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942783 | AAAGACTTTCCCCAG[A/G]TTATTCTGATGCCAC | 114792 |
| rs527805003 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898919 | TTCTGATCTCTGCTT[A/G]GCAAAATGAAGTAGA | 114792 |
| rs527809400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130398 | TGTATATAGTATACC[G/T]AGCCATGTGCTTTCA | 114792 |
| rs527811170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121883 | CTGAAGAACTTAGCT[A/G]ATGGTGGAAGGGAGA | 114792 |
| rs527821087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990606 | GTGTCCTCTCCAACT[C/T]GGAGGCAGCAGAGGG | 114792 |
| rs527834714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936679 | TCCTATAGACTCTTC[C/T]CCACACAGCAGCCAA | 114792 |
| rs527838136 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072248 | TTTCCACTACTACTG[A/T]CTTCAATCAGATCCA | 114792 |
| rs527838166 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080035 | CATTTGAAAAGATAT[G/T]AAAATCTTTTGATCT | 114792 |
| rs527860005 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036255 | TTACATTTCTCTAAC[C/T]TTCCCTTTTGTTTAT | 114792 |
| rs527873747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122904 | TGAACCTGGCCACTG[C/T]AGGTCTCCAAGACAG | 114792 |
| rs527876952 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971863 | AAAAAATTTTTTTTC[C/T]GTTGTTGAGACAGAG | 114792 |
| rs527897065 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985511 | CTTTCAAGTATACCA[A/G]TCAGACGTAGATTTG | 114792 |
| rs527899978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986285 | CAGTCTGCCCCTAAT[G/T]GGGGGGGCCTCCCAG | 114792 |
| rs527916605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025131 | GAGAAGACATCTGAT[C/T]CTGTGAGCCTGATGA | 114792 |
| rs527925736 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115147 | CAGCTTCCCAAATAG[C/T]TGGGACTACAGGAGC | 114792 |
| rs527935717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123663 | ATGACAGATGTATCT[A/G]TAGAAAGCTGTTAAG | 114792 |
| rs527961902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065786 | TTGACTTCTGTTACC[A/T]CTTAGGTAGTTTACA | 114792 |
| rs527963169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930815 | AGCTCCTGGAGCATC[A/G]GCCTGGTCACAAGGA | 114792 |
| rs527974915 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111300 | ACAAGAAGAGACAGA[C/T]CTGCATTTTACTCAC | 114792 |
| rs527985702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108688 | ACAGTAACACTTTTA[A/C]ATTTATGTGTTTATT | 114792 |
| rs528012305 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099693 | GGGCTCTCTGGGCCA[C/T]TTCTCCCACCCGAAC | 114792 |
| rs528015782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975124 | TATGGCATTACTTCT[A/G]TATTATTGTAGAATG | 114792 |
| rs528021672 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939074 | CAGTCTCTAAAGCTA[A/G]CAAACAACTATGAGA | 114792 |
| rs528027466 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011250 | ATGGGAGACATGTTC[G/T]TCTTTGAATCCTGCA | 114792 |
| rs528046109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102041 | TCGCATTCAGTCTTC[C/T]GTAGAACCCTATGAC | 114792 |
| rs528051573 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967417 | ACTATACATATATAT[A/G]TGTGTGTGTATATAT | 114792 |
| rs528060574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109357 | GAAATGTTGGAAAGA[A/G]ATAAGATAAAAATAT | 114792 |
| rs528105591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052927 | TCTTAATGTCTGCTG[C/G]GAAATTTCCATTACA | 114792 |
| rs528108186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102787 | CTGTAGGACATTTTC[A/G]CCATTTAAAAGTTTT | 114792 |
| rs528130154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011943 | TGTTTAATCCCCCCA[A/G]TAATCCTTAAATGTA | 114792 |
| rs528141782 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924401 | GGTGCCGGAGAGCGA[A/G]GAGGAGGGCGGCGTG | 114792 |
| rs528142666 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056356 | GTGATCCTCCCGCCT[C/T]GGCCTCCCAAAGTGC | 114792 |
| rs528151673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967825 | TGCCTTCCTGAGAAA[A/G]GCTGTATACCTGAGA | 114792 |
| rs528167933 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095326 | AAATCCAATAAAGTG[C/T]AAATAATGAAGTAAA | 114792 |
| rs528177372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103292 | GATCTCAGCTCACTG[C/T]AAGCTCCGCTTCCCA | 114792 |
| rs528186768 | in-del | -/C | 0.0178098 | 0.0926698 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984694 | AGACTAGGATTGCAA[-/C]CCCTGCCTTTTTTTG | 114792 |
| rs528206583 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139629 | AATTTATTGGACACA[A/G]TGGCATCGATGATCT | 114792 |
| rs528228698 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054566 | ACCTGAGTATGTTTG[A/T]TGCTTCAAAAGTTGC | 114792 |
| rs528230155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088104 | GTCTGAAATGACTTG[A/G]TCTGTTGGTTAATTT | 114792 |
| rs528239716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096013 | CAATTGGCTCATAAA[A/G]TGAGGCCCGGTTCAG | 114792 |
| rs528260749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960682 | CCCTCAGGAGATCCT[A/G]AGAACATGTGCCCAA | 114792 |
| rs528274793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991299 | GGTGTCTGCTCTGCA[A/G]TTCCAGCTGAAGGGT | 114792 |
| rs528281405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999041 | AAAAAATTTAAGGAG[A/G]CATCTAATAGGCAGA | 114792 |
| rs528288484 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951897 | AGTAGCGTTGTTTTG[A/T]TCAATGCCATTTCAT | 114792 |
| rs528290776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047325 | TGCTTGAATAGACCT[A/T]GGGATGCAGTGCAGT | 114792 |
| rs528304104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900246 | TTACACAGATTAAAA[A/G]TATGTGTCTAGTACA | 114792 |
| rs528315639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909683 | ATTTCCCATCCAGTG[C/G]TCTTTCCTTCTGTAG | 114792 |
| rs528320794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088798 | AACTTAGAACAACAC[A/G]TAGAAGTAATTCTGT | 114792 |
| rs528321251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952824 | GTCTTTTGAGATGTT[C/T]TTCAGACCTTTGTAT | 114792 |
| rs528328070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901154 | GTGGTTACTGCACTC[A/G]TGACTTTTGTCATTG | 114792 |
| rs528369259 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992176 | CGGGAGCCTGACCTC[C/T]CTTGTTGCCAGAGAT | 114792 |
| rs528390362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033386 | CTAAATAATGTTCGT[A/G]TGTGTGTGTATGTCT | 114792 |
| rs528394022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132938 | ATAAATTATTGAGCC[C/T]TATTAAAAATAAAAA | 114792 |
| rs528408279 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929790 | TTAAACGAACTATGT[A/G]GGAAAAAAAACAGTT | 114792 |
| rs528409867 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087403 | GCCAGAGGATTAGTG[G/T]CAGGGTGCTTTATAG | 114792 |
| rs528433078 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082202 | AGAGACAGGACTGGC[G/T]ATTGACTAGATGTAA | 114792 |
| rs528438553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938689 | TTTGGAAATAGACGG[A/G]CCTAAGCTTGAATCC | 114792 |
| rs528452709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074925 | TGGCAATCTCCTTAC[A/G]TGCTGAGTCAGGTTT | 114792 |
| rs528460202 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093945 | AAAAAGTCTGTAGGC[G/T]GTTGTCCCTATTTGA | 114792 |
| rs528463353 | in-del | -/CTTTGCTGTTGTTTGTCTGGGGTATATGC | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092761 | TAGCTTGACTCGTGG[lengthTooLong]CTTTGCTGTTGTTTG | 114792 |
| rs528467576 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141808 | ACAGATGATAACAGA[C/T]ATTCTTGGTGTTAAA | 114792 |
| rs528473094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111479 | AACCCGCTGCACCCA[A/G]CCCCTCATGGGACGG | 114792 |
| rs528494796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027652 | TTAGGATGATTTACT[C/T]TTTCAAAGACCATGT | 114792 |
| rs528499135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983144 | TGAGATAATCATGTG[G/T]TTTTTGTCATTGGTT | 114792 |
| rs528500410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987282 | GCTCTTGCTTCTCTA[A/G]TTCTTTTAATTGTGA | 114792 |
| rs528515550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939226 | GCCATTGGTGTTTTT[C/G]CTTATAAAAACATTG | 114792 |
| rs528516947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067589 | AAAGGGAACCACATA[C/T]ATTGAGGGCCTATCC | 114792 |
| rs528527884 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983713 | GTTTGTATTTCTGTG[A/G]GATCGGTGGTGATAT | 114792 |
| rs528538496 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925351 | CCGTTATTTATTTTG[A/G]TATTTAAAATAAAAT | 114792 |
| rs528564885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097395 | TCTTTCAGTTTGCCA[A/G]GAAGGTTAATTTGGG | 114792 |
| rs528593518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110785 | CGGAGCACGGGCAAT[A/G]GAGCTAGCTGGCTAT | 114792 |
| rs528633622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061358 | CAGCCCGCCCCATCC[C/T]GCCCCTGGATTCTGG | 114792 |
| rs528639934 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944693 | TATATTACTTGTTCA[A/G]GTTGCATGAGTAATA | 114792 |
| rs528640262 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921046 | TTCTCTGTAGCACTA[A/G]GTATTGTAATCTTTT | 114792 |
| rs528646863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926182 | GTAAAGATCCACTGG[C/T]ATTCAAGAATTAATT | 114792 |
| rs528690121 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061847 | CTGGCCAAACACAAA[G/T]TCCCTGGAAAAATAT | 114792 |
| rs528693541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055689 | TGTACTCCCAGCTAG[C/T]TGAGAGGTTGACGTG | 114792 |
| rs528722048 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006893 | CTCTTTTTAGGTGAC[C/G]AACCCCTTCTCTCTA | 114792 |
| rs528727121 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065446 | CCATTTCTTGGTTGG[A/G]TGAAAACTTCTTGTT | 114792 |
| rs528727217 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054441 | GTACATTGGTGCTTT[C/G]TCACAGTAGGTCAAA | 114792 |
| rs528728825 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096778 | AATGTTCTTACTGCT[C/T]TTAGAGAACTGTAAG | 114792 |
| rs528733943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048370 | ACCCATCTCTTGGGG[A/G]ATAGTCACCCTAAAT | 114792 |
| rs528744532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911089 | TTTTCTAGGGTTGCC[A/G]TAACAAAGTACCACA | 114792 |
| rs528748300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961819 | ATAATGGAGTTTTTG[A/G]CTCTCTGATATCAAA | 114792 |
| rs528755607 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056145 | AAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 114792 |
| rs528761363 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141341 | CCCCTCCTAAGTGAT[C/T]TTTATAATGTAATAT | 114792 |
| rs528771320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999984 | TGGGGAGGGAAAGAG[A/G]GCAGGAAAAGAATGT | 114792 |
| rs528788645 | in-del | -/GTT | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140296 | CTAAAAAATAATTTA[-/GTT]GTTGTACTAATTATG | 114792 |
| rs528804760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911656 | AGCTTTTGATTTCTA[C/T]CACTTTAAAGAAAGT | 114792 |
| rs528815858 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142416 | TAAAGAATATGCTAT[A/G]TTGCTAGCTTCCCAA | 114792 |
| rs528816312 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019392 | CAACGACAGCCTCAG[C/T]GGACTCCACAGGGAA | 114792 |
| rs528836412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090426 | GTGGTTTTTTTGACA[C/T]GCTCCTCCTGGGCTT | 114792 |
| rs528856251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041945 | TCATGGCTTTATTGC[C/T]TTAAAAACAAGACAA | 114792 |
| rs528879697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055879 | TCTCTGACTCTTCTC[A/G]CAGCAGAGCTTATGA | 114792 |
| rs528887983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947196 | GACTTTCCACCAATC[A/T]TATCCAAATAAGGCA | 114792 |
| rs528892371 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031949 | GCGACAGTTTCTATA[A/T]AACATTTACTATGTG | 114792 |
| rs528895746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993630 | ACCCTTCTCCTGTCA[A/G]GAACTATCAAAATTC | 114792 |
| rs528901758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082545 | ATGAACCCGGGAGGC[A/G]GAGCTTGCACTGAGC | 114792 |
| rs528915535 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042535 | TGTATATACTTATGT[G/T]ATGTAAATGTGATGT | 114792 |
| rs528917177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902632 | TTTTTGTTGCAATTG[C/T]TTTTGGTGTCTTCGT | 114792 |
| rs528934121 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011764 | AGGATATTAATGATG[A/C]AAGGATAGGCCAGAA | 114792 |
| rs528946859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034938 | TATAATCATGTTATC[C/T]GTGGAGGTAATTTCA | 114792 |
| rs528996471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077189 | TGCCTTTCCCTGGAG[A/G]TGGAATCTGATCTGG | 114792 |
| rs529005053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988668 | ACGTATGTTTATTGC[A/G]GCACTATTCACAATA | 114792 |
| rs529008782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940471 | TGATGCAGAATGCTG[C/G]TGATATCCAAAATGT | 114792 |
| rs529020073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984203 | TTTCGAGTCAGTTTC[G/T]TAATCCTGAGTTCTA | 114792 |
| rs529045720 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946018 | TTTTTAACTTTTTCT[-/G]GGGTCTTAGCTTTTA | 114792 |
| rs529058475 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069661 | TCCCTTCACATCGTG[C/G]GAGTTCATTATGTAC | 114792 |
| rs529070597 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969283 | AAATCACGCTATCAG[C/G]CATTTTACTCTTACC | 114792 |
| rs529114235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978755 | AACTAATTTGCATTG[C/T]CACCAGCAGTGTATC | 114792 |
| rs529127674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021504 | TCTTTTGATTCTATT[C/T]AGGCTTTCAGTTGAC | 114792 |
| rs529131520 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945849 | GAGGCTGGCATTGTT[G/T]TACAGTGTGGAATAA | 114792 |
| rs529133432 | in-del | -/ACATATAC | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943099 | CACATATATGCACAT[-/ACATATAC]ACATATACACATATA | 114792 |
| rs529135764 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070431 | ATCATAAGATCTGCA[G/T]TAGCCATTTTAGGGT | 114792 |
| rs529146378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120113 | GGTACCAGGAACAGT[A/G]AAGAGTCCTGAGGAT | 114792 |
| rs529149445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132288 | TCTAAAAAGCATTTG[C/T]GGGTATAGAAGAGGT | 114792 |
| rs529189512 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979575 | CTTGGGTAATGTGAC[A/T]TCAAACTATACTACA | 114792 |
| rs529190980 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989125 | AAATATTGACATGTG[C/T]GGATTTTCCTTTCAT | 114792 |
| rs529197781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971329 | GAACATCAAACCCTA[C/T]AGGATTTCTGTGACC | 114792 |
| rs529198379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105714 | GCTCTTCATGATGAG[C/T]TCTGTGATAAGAACA | 114792 |
| rs529227698 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971854 | AAGGGTAAAAAAAAA[A/T]TTTTTTTCTGTTGTT | 114792 |
| rs529260486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015864 | ATGTGCAGCCTTGGG[A/C]CTTGGTCCCCTGCAT | 114792 |
| rs529272445 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928285 | TTATAGCTATTGAAA[G/T]ATGGGAGTCTCCACC | 114792 |
| rs529283348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099246 | GACTGCACCCCTCAA[C/T]GGTGATATTCCCGCT | 114792 |
| rs529309017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008565 | GGCTGGAGTCCTGCT[C/T]CTGCCACCTCTCCTG | 114792 |
| rs529334553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964813 | AACAAACCTTTTCCA[A/G]TGGTGATTAATCCTT | 114792 |
| rs529343150 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099722 | ACTAAGCCCTGCCCC[A/C]CTGTCTCTGCTGCTT | 114792 |
| rs529345095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001879 | CATCTAGACGTATGT[A/G]TATGCCTAAGAAGAG | 114792 |
| rs529354443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920587 | ACACACACACACACA[C/T]ACATCTCCCTCCTTC | 114792 |
| rs529367058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913141 | TGCTAAGATTAGAAA[G/T]GACTATTAATGAGGT | 114792 |
| rs529381033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050583 | GGCTTGAAAGCCATC[C/T]GGAGTGAAATAACAA | 114792 |
| rs529393719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904965 | CTTCTTTCTTCACTC[C/T]AGCTTTCCCTGCTGC | 114792 |
| rs529399765 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964497 | TCTCTACTTAAAATA[C/G]AAAAAATTAGCAGGG | 114792 |
| rs529400724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092619 | TTTTATCCTTTGAGG[A/G]GCCCCTAGCTGGACA | 114792 |
| rs529408859 | in-del | -/AAAAAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968373 | AAAAAACAAAAAACA[-/AAAAAC]AAAAACAAAAACAAA | 114792 |
| rs529422108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136010 | GAAGTACAGAAGCAT[A/G]GTGGGGAAAAAATCA | 114792 |
| rs529426020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051347 | TTGGGAATAGAAAAA[G/T]AAATATTTCCTTTTT | 114792 |
| rs529451768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002523 | TGCAGGTTTGTTATA[C/T]AGGTAAATTGTGCGT | 114792 |
| rs529458890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136663 | CTGTTATCTTCATTT[A/G]CTATTATTTTTTTTG | 114792 |
| rs529465144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036179 | CTTCAGAATTTGTTT[G/T]CTTCATTTTTGTGGT | 114792 |
| rs529473618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949102 | GCATTTTAGCAGCCA[C/T]TGTTATCCAGTGTTT | 114792 |
| rs529501844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948682 | CAACATTATGTGATC[A/G]TAGATTTTGTGCATT | 114792 |
| rs529508949 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077880 | AATACAAAAAGCATA[C/T]GATGCGAAATCTACT | 114792 |
| rs529509786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044108 | CTTTTCACCACTAAG[C/T]ATAATGTTAACTCTG | 114792 |
| rs529510516 | in-del | -/CTCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917866 | TGTCCCCTAAGCTAC[-/CTCT]CTGAGACTGAGGTCT | 114792 |
| rs529512153 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108893 | TTTATACCTGCTTAA[A/T]TTTAAAAAACAGAGT | 114792 |
| rs529520251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128857 | GGCAGGCTTTGCAAA[C/T]CAGATGGCGTCCATA | 114792 |
| rs529528252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905885 | CATTTAGCTGCCTGA[A/G]GCTGTTTTTAAAATG | 114792 |
| rs529533060 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989466 | CTTTTGAAAGGCATG[C/G]TGTTAGCTTGATGGG | 114792 |
| rs529539594 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949154 | TTATTCTTCTTAGAA[G/T]GTAAGTTCTGTGAAA | 114792 |
| rs529541611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941566 | AGCAGAAGAGGTTTG[A/G]TATGATGTGATGACC | 114792 |
| rs529563125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121009 | TGTTAGAGAGCTAAA[C/T]GATTTAAAGGAAAGA | 114792 |
| rs529586458 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897432 | TTAGCGGGAGCACTG[G/T]CTGCTGCCTCTGGGT | 114792 |
| rs529596042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985719 | CCTTGGTTTTCAGTT[C/T]CATCAGGTCCTTTAA | 114792 |
| rs529612673 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976446 | CCATGGGAAAATGTG[A/G]CACTGTAGTGCTTCA | 114792 |
| rs529625228 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121666 | TTTAATGTCCAAATC[A/G]TTGGCTACAAAACTC | 114792 |
| rs529635303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079242 | TATTGAGAGACACCG[C/T]AAAGGCCATGGCCAC | 114792 |
| rs529647388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000196 | CTCAGGAAAATTCAA[C/G]AAAGTGGTACTATTA | 114792 |
| rs529664664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928981 | GAAGGCTTTGGTGAC[A/G]GATAAATGTACTATA | 114792 |
| rs529677970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113602 | TGAGTGCTTTTGTGT[C/T]TTTGCTGAGACGGAA | 114792 |
| rs529698153 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121226 | AACTCTGTGTCTCTG[C/G]TTCTTTAGACCATGC | 114792 |
| rs529710268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921745 | GTTTTAGCTAGAAAT[A/C]TGATCTGTGTAGAGA | 114792 |
| rs529710885 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977784 | TTTTTTAAAAAGCGT[A/G]TTAAATGTGATGAAA | 114792 |
| rs529715265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064442 | AAATTGGCTGTTAGA[A/G]TAAGGGCCACAGCTC | 114792 |
| rs529716796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985911 | CTTTGTTCCATTGCT[G/T]GTGAGGAGCTGTGTC | 114792 |
| rs529718803 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023871 | GAATCTGGTTCAGAA[A/G]AGAGTCCTGAAAAGC | 114792 |
| rs529736156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936442 | CTACCTCATCCAGAG[C/T]CTCTCCATTTTTGGT | 114792 |
| rs529763338 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090385 | GACATAAGCCACATA[C/T]TGTTTAGTCAACAAT | 114792 |
| rs529764713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107665 | AACAAGGGCTTATGA[A/G]TCTAAGTTTAGGGCA | 114792 |
| rs529778839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065052 | AAGGAGTCCTAGTCC[A/G]AAGCAATATTGTCTG | 114792 |
| rs529805770 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009857 | AGATTATATGTTTTT[A/G]AGACACTATAATTAA | 114792 |
| rs529826693 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092249 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 114792 |
| rs529857248 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955999 | AAAGACGGATGTTTA[C/T]TGGACTTACAGTTCC | 114792 |
| rs529857315 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932461 | AGCATTTAACTTGAC[-/T]TTTTTTCTGAAATCC | 114792 |
| rs529882843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914711 | TTTAGAGACAAGGTC[C/T]CATTATGTTGCCCAG | 114792 |
| rs529889519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059042 | CTCCCAAGTTGATTC[C/T]GTCAGCAAGTGTAGG | 114792 |
| rs529890870 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045034 | GAGGCTTATTAAAAC[A/G]TATGATATCATTTAT | 114792 |
| rs529917252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958837 | TGCCAAGGAAAAAAA[A/C]ATCACCCTAAGTTAT | 114792 |
| rs529934706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101651 | GTTCATGCTTCTCCA[A/G]CGTTGAATTTAACAA | 114792 |
| rs529955282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950324 | GCTCATTCTAGCAAA[C/G]AGAAGAGTGGGATGT | 114792 |
| rs529965744 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909161 | ACAAGAGGGATACCA[A/G]TTGACCTGCCTTGGG | 114792 |
| rs529968637 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898077 | CCCAGACCCACGGTT[C/G]CTTTTAACGCTGGAA | 114792 |
| rs529974708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138637 | AAACCTTCCAGAATC[A/G]ACTGAATTTTGAATT | 114792 |
| rs529982334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003855 | TTGGTCTATGTCTCT[A/G]CTTTTGTACCAATAT | 114792 |
| rs529988419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967286 | ACCTAAATATGTTTC[C/G]TGATTCTTTGAATGA | 114792 |
| rs530011145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959138 | TTGAAAGCTGGGGGC[C/T]AGATGCTCCAAGAGG | 114792 |
| rs530024180 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083750 | ATTACTTTTTATAAC[G/T]AGAAATGGCACTCTT | 114792 |
| rs530029694 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936459 | TCTCCATTTTTGGTT[G/T]TTCAGCACCCAAACC | 114792 |
| rs530033670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130525 | AAAATGCAACACAAA[C/T]TAGAGGAGATGCCGT | 114792 |
| rs530055422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080157 | ATTATACTTGTTCAG[C/T]AACACTTTCAACTCT | 114792 |
| rs530061752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926602 | AAAAGTTGTGTGTGC[A/G]TTTCAGATGTGTGCA | 114792 |
| rs530068503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087277 | AAAATCAAATCAGAC[C/T]GCTATTTTGCCTCAA | 114792 |
| rs530068749 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943397 | AAGTAAAAAAAAAAA[A/C]AAAACCTTATACTGT | 114792 |
| rs530084011 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056198 | GGAAGCTCCGCTTCC[C/T]GGGTTCACGCCATTC | 114792 |
| rs530102931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951006 | GTTTGAACAAAAAAA[A/G]AGTACTTCTCACAAA | 114792 |
| rs530109313 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915969 | TTATCATTAGCGACA[A/G]AAAGTGTTAAAAGAA | 114792 |
| rs530120691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990730 | TTGGCCCAGAGTTGG[A/G]CAGCTGTGTTATGGG | 114792 |
| rs530133828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986307 | GCCTCCCAGTTAGGC[C/T]ACTCAGGGGTCAGGG | 114792 |
| rs530151760 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943908 | AGCCAGCTTCTTCAG[A/C]TCTAGATTCAAAAGC | 114792 |
| rs530153698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937215 | AAATGTTCCCTCATG[C/T]CCATTTGCAGTTATT | 114792 |
| rs530167401 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131268 | GAACCAGACACTGAA[C/G]GATTTAATAACTCTT | 114792 |
| rs530170235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123037 | ATCCCACTCTGTCCT[A/G]GTAGTGCGTTAGCAC | 114792 |
| rs530188860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938046 | TATGTATTTCTGATT[C/G]CTAAGCCTCTTTGTC | 114792 |
| rs530225693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930981 | CATCAAGTACCTGGC[A/G]GGTACAGACCTCCTA | 114792 |
| rs530252117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986602 | CAGCCTGGCTGCTGC[C/G]TTGCAGTTGGATCTC | 114792 |
| rs530255658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073944 | GCTGCACATCAAGGG[A/G]CATGTGCCACAGGCC | 114792 |
| rs530256685 | in-del | -/AAC | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955938 | CAAGACTCCATCTCA[-/AAC]AACAATAACAACAAA | 114792 |
| rs530277995 | in-del | -/TT | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962232 | AGCAACTTTGAAACA[-/TT]TTAATAAAAATAAAG | 114792 |
| rs530297700 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067359 | CAGCTATTTAATTAG[C/T]CCCCTAATTAGCCTT | 114792 |
| rs530323827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931557 | CTTATACCTGGTATG[A/G]ATGTATGCATATGTT | 114792 |
| rs530352617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053727 | TACATTTGTTTTTTT[A/T]AATTTATATACTATG | 114792 |
| rs530352902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060728 | TATTCAAGAGTGCCT[C/T]CTACCAGGAGGGTGA | 114792 |
| rs530366102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117011 | GTGTACAGTACAATA[C/T]CTTTAATTGGAAAGA | 114792 |
| rs530407290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925236 | CCCTTTCTTCCCTCC[C/T]CCTGAGCCCAATATG | 114792 |
| rs530407383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960201 | CATTGTCATCACCAT[C/T]GTTTCCTTTTAACAC | 114792 |
| rs530411832 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968390 | AAAACAAAAACAAAA[A/C]CAAAAAAAAAAACAT | 114792 |
| rs530428057 | in-del | -/TA | 0.00318978 | 0.0398085 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924862 | CAAACACGCTAGGAC[-/TA]GCTCGTCTTCGCTAC | 114792 |
| rs530431465 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012032 | GTAATCAATCACGTA[A/G]CTGCTGAATGCTAGA | 114792 |
| rs530459408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096080 | CAAGACTGTTATTTT[A/G]TAGGTCTTCTTTTTA | 114792 |
| rs530468768 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012708 | AATCCTGGTCTCATA[A/G]TGCCACCTGAAAATG | 114792 |
| rs530492877 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960811 | CAGCTGGAAGCGGGG[G/T]CTTCTGGGTCATAGG | 114792 |
| rs530500396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103344 | TCAGCCTCCTGAGCA[A/G]CTGGGACTATAGGCA | 114792 |
| rs530514480 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054704 | GCATTTATTCTATAG[C/T]AATTGAATAGACAGA | 114792 |
| rs530539812 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092952 | CTCATGAGTTAATAG[-/T]TTTTTTTTCTTTCCT | 114792 |
| rs530549128 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132589 | TCCCTCAGTGGCAAA[A/G]GGGTTAATTAAAATA | 114792 |
| rs530569282 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005976 | TACAGAAGAGAAGAA[A/T]GTATATGCTCTTGTT | 114792 |
| rs530586753 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992229 | AGGGGATCCATGGCT[C/G]CCGGGACCCAGGGTT | 114792 |
| rs530590258 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981933 | TCGGTATAATGTCAG[-/T]TTTTTTTTAATTTGC | 114792 |
| rs530606570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999134 | GGCATGGATACTCAT[A/G]CCTGTAATCTCAACA | 114792 |
| rs530607069 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964417 | GCAGCGCTTTGGCAC[G/T]CCCAGATGGGTGGAT | 114792 |
| rs530609515 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087726 | GTGGCTCTTCTACTA[C/T]GTACTGATAATGTCA | 114792 |
| rs530637136 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040610 | AGGTGATCCTGATGT[C/T]GCTGGTCCAAGGGCT | 114792 |
| rs530651911 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945754 | GTGGTAGCTTCCCGG[C/G]GGAGTCACAGGCTTT | 114792 |
| rs530653633 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141096 | AGGACTTAAGTATTC[A/C]GCTATATTAATTTTT | 114792 |
| rs530691135 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898880 | GTATTTCTCTTACTG[C/T]GGCTGCAAAATCTAT | 114792 |
| rs530704650 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101615 | CTCTCCCTTTTCATT[C/G]ATTCATTCATTCATG | 114792 |
| rs530705883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987310 | TGATGTTAGGGTGTC[A/G]ATTTTAGATCTCTCC | 114792 |
| rs530722574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133186 | CTTCACGGCAGAGGC[C/T]GTGAGCAGTAGTGGT | 114792 |
| rs530724103 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033603 | TTTAGTACCCTCTCT[A/T]CTGTTTCCCATAATG | 114792 |
| rs530728942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118113 | AGGACATTTGTTAAG[G/T]CTTAACTCCCTAGAA | 114792 |
| rs530730679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126345 | CTATGCTGTTTTATG[A/T]TTTTTTTTTTTAGAG | 114792 |
| rs530748510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082335 | AAGCTCAGTTTAGGC[C/T]GGGAGCGGTGGCTCA | 114792 |
| rs530761548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033967 | CTTGCAAATATTTTT[C/T]CCATTCTGTGGGTTG | 114792 |
| rs530791018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110968 | CTTAACATTATAAAA[C/G]AACAGATAAGGAGCC | 114792 |
| rs530792854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118606 | CCTGGGCAAGAAAAG[C/T]GAAACTGCATCTCAA | 114792 |
| rs530826079 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127749 | AACGTCCTTCTGGAA[C/G]GGGCTGCCATTCTAG | 114792 |
| rs530845456 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896243 | TATGGATTTACACAT[A/T]GGTTCCCATTCCTAA | 114792 |
| rs530858055 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027804 | AGCCTACAAAACTTC[C/G]AGCATTGGCTTCAAG | 114792 |
| rs530858291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020440 | TAGAAAAATGTAATT[A/G]TCAAAAGTGGGCCTA | 114792 |
| rs530860386 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098137 | TTGAAGTATAGGCTA[A/C]AAACGATACAGACAT | 114792 |
| rs530861339 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013881 | AATATTTGTCAAAAG[G/T]GATAAATGCTCATTT | 114792 |
| rs530865144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068288 | CTTTTTAATAATATG[A/C]AATTTAAATGTATTG | 114792 |
| rs530884457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113086 | CTGTTTTTGTGCAAA[C/T]GACTCTAACAAATTT | 114792 |
| rs530897256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014269 | CACTGCACTCCAACC[C/T]GGGTGACAGAGCGAG | 114792 |
| rs530897630 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943089 | GTACATACACACACA[C/T]ATATGCACATACATA | 114792 |
| rs530934066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061467 | CTAGCTGTGATATGC[C/T]CCTCCAGACTGATGA | 114792 |
| rs530938674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926320 | AATAAATAATGTGAG[A/G]AGCAAGTAAGCCAAA | 114792 |
| rs530970786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934014 | GGATAACACAGATAA[C/T]CTCACTTTTCTCACA | 114792 |
| rs530984985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969249 | GACCTTGTTATCCTT[A/G]GTAATTGCTCTGTTT | 114792 |
| rs530988876 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056157 | GTCACCCAGGCTGGA[C/G]TGCAGTGGCACGATC | 114792 |
| rs531000238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056322 | ATGTTAGCCAGGATG[A/G]TCTTGATCTCCTGAC | 114792 |
| rs531012940 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142676 | TGCTATGATAACATA[C/T]GGTTTGGGGAAGGCA | 114792 |
| rs531035602 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923476 | CAGGACTGCTAGATA[A/G]GTAGGTACCCAGCAT | 114792 |
| rs531035756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104822 | ATGCTCTGATGCTGC[A/G]TCCCTAGTTTCTGGT | 114792 |
| rs531062050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042010 | CTTGGTACCATGTCC[A/T]CCACATATCTCAGAG | 114792 |
| rs531063472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049782 | CTAGTTATTTGCCTT[C/G]GGGTAGATTTTCTCT | 114792 |
| rs531067983 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912364 | CCTTGCTTCTCAGTT[C/T]GTGCTTTCTCTGTAG | 114792 |
| rs531071128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970212 | TCTGGCCCAGTCTCC[C/T]CTACTGCTCTTGGTA | 114792 |
| rs531107944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962673 | AATAAAAGAAGACAC[A/G]CAATGATGTTTACTG | 114792 |
| rs531142859 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901369 | GGAAGGGGTTCTTCT[A/G]GAGACTTCCCGCATT | 114792 |
| rs531154594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090548 | TATCCCTTTACAGTT[G/T]GAAAGTAGAAGACAC | 114792 |
| rs531176600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994418 | TACAAATTATTTATG[G/T]TTTTTTTCCTTTTAG | 114792 |
| rs531177328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000650 | CTAGACATCAAATAA[A/G]ACTTGCAAGAATGGG | 114792 |
| rs531203004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947802 | ATAGAATGAAGAAAC[G/T]GAGGCAGAGAGGAAT | 114792 |
| rs531203606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035567 | CCTGGGAAAGACTTT[C/G]TCTTTCATTTATTTT | 114792 |
| rs531211366 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083191 | GGTCAGGAGTTCAAG[A/G]CCAGCCTGACCAATA | 114792 |
| rs531244121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947234 | AACTGTAGCCAATCA[A/G]GTAATTTCTTAGTTT | 114792 |
| rs531263341 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128045 | TAAAATATGGATGAA[A/C/G]CTTGGCAATTGCCTG | 114792 |
| rs531266632 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135202 | TATTTCTGTGTTCCA[G/T]TAGCCATTCTGATGA | 114792 |
| rs531321386 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096240 | CTGTCCTCTGTCACT[G/T]ACACATATGCAGGTG | 114792 |
| rs531330383 | snp | A/G | 1.65315e-05 | 0.00287498 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127359 | ATGTTGGAATATCCT[A/G]TTTTTTATTCATGAA | 114792 |
| rs531345547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070521 | AGGATGTCAGGAAGC[G/T]ACAGCCCAGAGGCAC | 114792 |
| rs531351288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077317 | TCACAAATAATAATC[A/G]TTTGTGACAAAAGAG | 114792 |
| rs531355236 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915135 | AGCTTCCCATTATTT[G/T]GCCTCAACTTTTTCT | 114792 |
| rs531362259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934846 | CACTGTGGATATAAT[C/T]TTATGGGTCATTGAT | 114792 |
| rs531382876 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067337 | TGCTCCTCTGTGTCA[A/T]TGAGGACAGCTATTT | 114792 |
| rs531405736 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969419 | CTCATTTTCCTTCTT[A/T]AGCAGTTTAGATTCT | 114792 |
| rs531409902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928305 | GAGTCTCCACCAGAC[A/G]GTCTGTTGGAAATGT | 114792 |
| rs531425973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979674 | TATGAATTTTAGAAT[A/T]GGTTTTTTCTAATTC | 114792 |
| rs531429263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984708 | ACCCCTGCCTTTTTT[A/T]GTTTTCTATTTGCTT | 114792 |
| rs531447806 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120254 | GGTGTGAACCTAGGT[A/G]AGCTCACAGGTGAGG | 114792 |
| rs531459530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021646 | CCAAATATCTAAACA[C/T]CTGTGGCAAGTCAAA | 114792 |
| rs531466190 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985165 | TGAAATTCTGGGTTG[A/T]AAATTCTTTTCTTTA | 114792 |
| rs531467375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978816 | CATCTGCTATTTTTT[C/T]ACTTTTTAATCATAG | 114792 |
| rs531470905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064226 | ACCTGTTTCTGTGGT[C/T]TACTAAAGAGCAAAA | 114792 |
| rs531474771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920837 | CTCAAATATTACCAA[A/G]CTATCATGAGTATCC | 114792 |
| rs531509174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112639 | CTTAGTAAAGACAGG[G/T]TTTCACCATGTTGGC | 114792 |
| rs531522406 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013789 | AAAGGAAGAAAACAG[C/T]GTATTATGGGAGTCA | 114792 |
| rs531544720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964875 | AATTTCAACTTTTAT[G/T]TTGGATTTAGCATGT | 114792 |
| rs531546175 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949057 | AACACAGTAAACACC[A/T]GTTGACTCAATCACA | 114792 |
| rs531571259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099822 | GAACCCAAATCCTTT[G/T]ATATGACTACCTGGG | 114792 |
| rs531584919 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015931 | GACCATTGCTTCAGA[A/G]GGCACAAGCTCCAAG | 114792 |
| rs531600229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051391 | GTTTTATTGTCATAG[A/G]TGGGGCAATAAACAG | 114792 |
| rs531618154 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002552 | GTCATAGGAGTTTGG[A/T]GTACAGATTATTTCA | 114792 |
| rs531622868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016381 | CTTAGATGTGAGACA[C/T]GGCGTCAAAGGAGAT | 114792 |
| rs531631284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092694 | GAGCATATATTTAAT[C/T]TTTCCTTCTAATCTA | 114792 |
| rs531641060 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006694 | AGATCTTGTGGTAAT[C/G]AATTCCTGTACCATT | 114792 |
| rs531662195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044177 | TCTTTCTATGCCTAA[C/G]TTGTTGAGAGTTTTT | 114792 |
| rs531701817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002017 | TGTAAAGAACTGGCT[C/T]ACATGATTATGGAAC | 114792 |
| rs531706402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995758 | AATATGATGTCTCTC[A/G]TGAAGCCCTATCCTG | 114792 |
| rs531712797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921580 | TAATTAGAAATATGG[C/T]TCAGTGATTCCTTAA | 114792 |
| rs531717195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913232 | ACACCCCAGCAACTA[A/C]TAAACTGAATTCTGC | 114792 |
| rs531719235 | snp | C/G/T | 4.94395e-05 | 0.00497169 | intron-variant, missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041545 | TGAGGTTAATTTGCA[C/G/T]GGTGTGACCAGCCTT | 114792 |
| rs531722627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989519 | GCCCTTTATCTCTAG[C/T]TGCCTTTAATATTTT | 114792 |
| rs531728074 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897468 | AAGTAGGCGGGGCCG[A/C]CGACCTCACCGCGGG | 114792 |
| rs531753132 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086326 | GCTAACTCTACTGAC[G/T]GATTATTTTCCTGAT | 114792 |
| rs531780671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913816 | CAGGCTGGCACTGTC[C/T]CCTCCGTCATGGGGG | 114792 |
| rs531780895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905122 | AGCAATTTAATCAAT[A/G]CAACAGTTGTCCATC | 114792 |
| rs531804465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136942 | TCCTTGCTCTTTCTG[A/G]GTTGCGTCTTGAGCT | 114792 |
| rs531810987 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944717 | AGTAATAAGTTGTGA[C/G]GTTAGAAGACGAGAT | 114792 |
| rs531811770 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079364 | AAAGGCCACAGGATC[A/T]ACACTGTCCTCAAAC | 114792 |
| rs531821504 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981217 | ATCAGTAGGCTTCTT[C/T]TTACTGATTCAATTT | 114792 |
| rs531859022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128923 | ATTGATTCCTAATAC[C/T]GTAATGGGTTGTTTC | 114792 |
| rs531868425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137831 | GCCACCGCGCCCAGC[C/T]TATTGCAGTTAAAGT | 114792 |
| rs531874938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079722 | AAATAGAAGGAATAA[A/G]AGAAGCCAAATAGCC | 114792 |
| rs531878711 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956559 | TCCATCCTTTAGTGC[G/T]CCCCTACTTGGTCTT | 114792 |
| rs531893795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078924 | AAGCCAGGGAGCCAC[A/G]GCGGTAGCCAAAACT | 114792 |
| rs531894929 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948704 | TTGTGCATTAGGAAA[A/G]TTAGGATTGATGAAG | 114792 |
| rs531896680 | snp | C/T | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114506 | GGTCTTCTTTGGATA[C/T]CAGGTAGAACATACC | 114792 |
| rs531904089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002282 | ATGAAGCCCACTCAC[A/G]TTAGAGAAAGCAATT | 114792 |
| rs531933327 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092661 | TGCTATTTCAGGGAT[C/T]GGTGCTCCTAGTTGC | 114792 |
| rs531935097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024254 | CATCTGGTAGATATT[C/T]GATAAGCATTAATTG | 114792 |
| rs531956957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114994 | GCATTGAGAGAAGGG[A/G]TTTAAGTTACCAAAA | 114792 |
| rs531960179 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897976 | CGCTTCTCTGCCCAG[A/G]GCATTTAAAAGGGAG | 114792 |
| rs531963792 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954441 | CACATGGGCAGGCTT[A/G]TTATGCAGCGATTAC | 114792 |
| rs531967117 | in-del | -/GCGGG | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924465 | TGGCAGCTCGCCGAC[-/GCGGG]GGCGGGGGCGGGGGC | 114792 |
| rs531968296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942753 | AGAGAGGGGAGAAAG[C/T]ATAGAGAGATTGAAA | 114792 |
| rs531973988 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017124 | TTAAAGTCAGTATGA[C/G]TGGAATTTGGTGAGT | 114792 |
| rs531977142 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031007 | CCTTCATGGAGCCTG[A/C]ACTCTACCTTTTCAA | 114792 |
| rs532000836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981812 | TTTCATTGTTTACCC[A/G]AAAATCATTCAGGAG | 114792 |
| rs532002582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126072 | GTTAAGGCCCTCTTG[A/G]TCAGCATTTTAACAG | 114792 |
| rs532023148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010249 | AGAAGCAATGGATCA[A/G]CAGAATGGGTATAGA | 114792 |
| rs532032142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974222 | ATAGTTCATGGGACA[C/T]GGTAAGCACTATGTG | 114792 |
| rs532049691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122634 | TTATAGTCTTTCAAG[A/T]ACTGGAGAAAGTTTA | 114792 |
| rs532065386 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936473 | TGTTCAGCACCCAAA[C/G]CTTGGAAACATCCTT | 114792 |
| rs532067339 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129122 | TAAATGCAAGCTTTT[C/G]AAGCTGTACAAATCA | 114792 |
| rs532073705 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905714 | ATTCTTTTATATAAC[A/G]AAATACTAATATAAT | 114792 |
| rs532084446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065149 | AGTAAATCACAAAGT[C/T]CTATGTAATTAATTA | 114792 |
| rs532090304 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063990 | GGTATCACCAGGATA[C/T]TTGGGAGGCATTACC | 114792 |
| rs532094523 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095742 | GCCCGGGAGCACACA[A/G]GAAGTAAAGTGATCT | 114792 |
| rs532110894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101842 | TATAGCAATCTCTCA[A/G]AATTTACATCACTAA | 114792 |
| rs532117233 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939731 | CACAGGCCTATAAAG[A/T]TAGGTATCTTTATCA | 114792 |
| rs532132422 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938078 | AGTAATGAATAATTT[A/T]AAACAAACAAACAGA | 114792 |
| rs532148745 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956360 | AAGGTCACATAAGCA[C/T]TATTGGAGCCAGAAT | 114792 |
| rs532152103 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066561 | CACTGACTTTTCACA[A/G]ATGTTTTCATTTTGT | 114792 |
| rs532170589 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916928 | TATAATCAACCTATG[A/G]AAAAATGCATAAAAC | 114792 |
| rs532186315 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044452 | GTTCATCATGGATAT[G/T]GGCCTGGAATTTTCT | 114792 |
| rs532200523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045888 | CATATCCCATTGCCC[A/C]GGAGTCATATGCCTT | 114792 |
| rs532216052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997409 | CATATGTATGCATTG[G/T]TTAAGACATTAGTTT | 114792 |
| rs532229090 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908689 | AGAACTTAGACATCA[A/T]CTAGGATAATCAGCT | 114792 |
| rs532229099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038541 | GATATGGAGAAAGGG[A/G]AACCCTAGTACACTG | 114792 |
| rs532239295 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139540 | ATATTGTGTTCCATG[C/G]GTCTTTAGAGCATTC | 114792 |
| rs532278253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951179 | GTCTCGGTTTGATGA[C/T]AAGGGAGACTTCAAC | 114792 |
| rs532292054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967348 | GATGCTAACTTCCCT[C/T]AAACATGAGGTATGC | 114792 |
| rs532299729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131464 | CTGCATTTTTGGCCA[C/T]AAATACCCATCCAAG | 114792 |
| rs532301029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990789 | TTGGTGATGAGCAGG[G/T]AGCATTGGAGGCTCA | 114792 |
| rs532313448 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075704 | TCCTGGAGTACCAAC[C/G]TTTCCTGCAGCACCA | 114792 |
| rs532316783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943461 | TGACACCTGTTTTAC[C/T]TATTACTGCTGACCC | 114792 |
| rs532331674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959290 | TGTGGTCTGCAGGCC[C/T]GGGACAGCTTCTGAG | 114792 |
| rs532351207 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912147 | AGCTCAGTGGTGGCC[A/G]TCACCTCCTCCCTAG | 114792 |
| rs532376610 | in-del | -/TGTTTT | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902248 | AATCTTGCCAGCATC[-/TGTTTT]TGTTTTTGTTTTTGT | 114792 |
| rs532383410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087374 | ATATTCAGCCCAGAG[G/T]AGAGATTGGGTATGC | 114792 |
| rs532391926 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046678 | GACATGGACACAGCT[G/T]ATGGCAAAAAGAATG | 114792 |
| rs532405166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026004 | CTTTCTTTTAATGAT[A/G]GAGCAAAGCTCATTT | 114792 |
| rs532421924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960032 | TTCACTATTTATTAC[C/T]TGTGTGTCTTTCAGT | 114792 |
| rs532422797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074079 | AGGCCTCGGGTCACA[A/C]AGTTTGTTTGCTGCA | 114792 |
| rs532429988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997872 | AAACAGCTTGAAGGT[A/G]ACAGTACTGCTGATT | 114792 |
| rs532437379 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945498 | GTTTAATTTCCAAGT[A/G]CAGCACAGTGCCTAC | 114792 |
| rs532437672 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905321 | TATGTGAAAAGCAAG[C/T]TGTAACCAAAGCATT | 114792 |
| rs532439164 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039912 | AGCATAAAGAAAAGA[C/T]ATTTTAAGGTGATAG | 114792 |
| rs532446682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087988 | TGATGCCTTGGAACT[A/G]TTCTTTTTTTTCCAT | 114792 |
| rs532454212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039367 | ATAGAGTAGATTGGT[A/G]GTTACCCTACCCAGT | 114792 |
| rs532469189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991187 | CAAGGGCAGGACCAG[C/T]GCACTGGCGGTGGCA | 114792 |
| rs532469802 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018346 | AATTTGGCCAGGCAC[A/G]GACACCAAGGCAGGC | 114792 |
| rs532485091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066643 | TTGTAGAAGGAAATT[C/T]TGACTATATGAGTAT | 114792 |
| rs532490298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026658 | GGGCATCTATATTTA[C/T]GGTCATATACCTTCC | 114792 |
| rs532499360 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997186 | CAAGCAAATGAGGAA[A/G/T]GCTATGTGTATGAAG | 114792 |
| rs532511523 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080861 | GGAGAAATGTGATTG[A/G]CGGTGACATGGAGAG | 114792 |
| rs532518508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018690 | CTAACAAAAACATAT[C/G]TGTAACAATATTAAT | 114792 |
| rs532522598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938646 | GCAGCAGCAGCAGCA[A/G]CAGCAGGGGATACAT | 114792 |
| rs532535801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944065 | TTGACCCCCAGCTGT[A/G]TTCGTTCCCTGTCAG | 114792 |
| rs532538699 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976266 | AACCAGGAGCCAATT[A/C]GGTGGTACCCCCAGA | 114792 |
| rs532569168 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925278 | TTGGTTGCCAAGGAG[A/G]CTTGCTTAAACATCA | 114792 |
| rs532574611 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081476 | GGCAGTCTATTCTCA[C/G]TCAGTGAAACCCCAG | 114792 |
| rs532593553 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000434 | AGCATGTAGTAAGTT[C/T]ATTTGTGTGCTGGTA | 114792 |
| rs532607414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982615 | CTTGTAAGTTGGATT[C/T]CTAGGTATTTTATTC | 114792 |
| rs532624183 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074753 | ATGACTTCTATACTA[G/T]TCTTTTAAACATTTT | 114792 |
| rs532637855 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054783 | TATCTGTCAAAGTAG[G/T]AACAACTTGGCACAG | 114792 |
| rs532637937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061299 | AGAGGCAATGCCCAA[C/T]CTAGTTTGGCTTCTT | 114792 |
| rs532641386 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044289 | TTAATATGGTATATT[A/G]CATTTATTTATTAAT | 114792 |
| rs532697055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983082 | TTGTTGAGAGTTTTT[A/G]GCATGAAGCGTTGTT | 114792 |
| rs532699317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096138 | CATTCTCACACCCAA[C/T]GTAGCTAATAAAATG | 114792 |
| rs532703148 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020187 | ACCTCATGATCCACC[C/G]GCTTCGGCCTCCCAA | 114792 |
| rs532726315 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047639 | TTTTTCATGTTTCAG[A/C]CCAGTCCTGAGTAGA | 114792 |
| rs532733223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110134 | TCTCCACTTCTGGCA[A/G]AGACCTGGTGATTGA | 114792 |
| rs532750749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961754 | GTAATTGAGCTGTAT[C/G]GTTCTTCATAGGATA | 114792 |
| rs532771495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917927 | GAGGTCAGATAATTC[A/T]TTGTTGCAGGGGCTG | 114792 |
| rs532796764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110703 | CTGATTCCATGGTTC[A/G]AAAAGGAAGTAAAGC | 114792 |
| rs532803496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916925 | AAATATAATCAACCT[A/G]TGGAAAAATGCATAA | 114792 |
| rs532857822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103841 | GAAACCTGTGACTTG[G/T]GTACTAGATTAATTT | 114792 |
| rs532884106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090261 | CTAAGAAAATTGATA[C/T]AGAAAATGAGTTTGG | 114792 |
| rs532906831 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096672 | GTCCCTTTCCTACCA[A/G]TTGTGGTTCCCACCA | 114792 |
| rs532912660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125938 | ATGATTTACATCTCA[A/G]AGAGGGAGAGAAAGA | 114792 |
| rs532921537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082529 | GAAGCAGGAGAATGG[C/T]ATGAACCCGGGAGGC | 114792 |
| rs532923534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075736 | GTTAGGTAGTCACAT[A/T]ATACCTTGATTTATA | 114792 |
| rs532931033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999209 | AAGACCAGCCTATGC[A/G]ACATAGGGACACCCC | 114792 |
| rs532932374 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018426 | CCCTGTCTCTACTTA[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs532934207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048252 | TGAACCAATTATGTC[A/G]TATCCGGGCTTCTGA | 114792 |
| rs532948799 | in-del | -/CTTGGCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010295 | GCAGCAGCAGTGGTG[-/CTTGGCT]CTGGTAGGGCTGGTG | 114792 |
| rs532954080 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008706 | CCTTCCCCAGGAGAC[A/G]CTGGAGCCCAGGAAT | 114792 |
| rs532958274 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141327 | CAGCATATATTAAAC[C/T]CCTCCTAAGTGATCT | 114792 |
| rs532966111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999867 | CCGAGCGTCTACTAC[A/G]TGCAAAAAAGTTTGT | 114792 |
| rs532975744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983781 | TTCTTTTCTTCTTTA[C/T]TAGTCTTGCTAGCGG | 114792 |
| rs532980878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947037 | TTAAAGCATTTGTAA[A/G]TGTTAAAAGAAATTT | 114792 |
| rs532984045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030545 | CTGTGATGACTGTAA[A/G]TCTCAGCCTGGCCGA | 114792 |
| rs532988425 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037222 | TTTAGTGTTTCTAAC[A/G]GTGAAAGGTTTAACT | 114792 |
| rs532995040 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052240 | GGAGAATCACCATGA[C/T]TGGGACAGCAGATGC | 114792 |
| rs532996068 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989883 | GTCTATTCTGCTGTT[A/T]AAAAAAAGTGCGATT | 114792 |
| rs533000997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041209 | CCAAGAGAAAGCGTT[C/T]GGTGGGCCTAAATAC | 114792 |
| rs533066996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034099 | CCAAAAAATTATTGC[G/T]TAGACCAATGTCAAG | 114792 |
| rs533073179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902478 | AAATTTGTTTATAGG[C/T]GTTGCATATTGGACC | 114792 |
| rs533082280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987403 | CCAGAGATTCTGGTA[C/T]GTTGTGTCTTTGTTC | 114792 |
| rs533093230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119168 | TGGCTCTACCTGTGG[A/G]AGGAGGACAATTAGC | 114792 |
| rs533097800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978076 | GTCTTTTAATGGACC[A/G]TAATATAGCCTTCTT | 114792 |
| rs533137119 | in-del | -/G | 0.212122 | 0.247114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027570 | TCAACCAAAATAATT[-/G]GGGGGAAAAGGGAGA | 114792 |
| rs533137820 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104976 | CAGTTGCTATTCTGG[C/T]TTATGACACCATTAT | 114792 |
| rs533137933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978652 | TGTAATACTTTAGGT[A/C]TATACCCAGTAATGG | 114792 |
| rs533140366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126652 | TGACTTATTGAATCC[C/T]TGAAGCATGGCTAAT | 114792 |
| rs533156408 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034876 | GTTAAACTCATTTAT[A/T]AGTTCTAACATTGTT | 114792 |
| rs533195066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105579 | AAAGAGAAGGGCTCC[A/G]TGTGCACCTTCAGCA | 114792 |
| rs533201611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007376 | CCATTTCATCTTTTC[A/G]CTCCTGTTTCATTTT | 114792 |
| rs533207978 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118697 | TGAGTTGTGGTGCAC[G/T]GAGACCACAGACCGT | 114792 |
| rs533220200 | in-del | -/TA | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142186 | ATATACTTTTATTAT[-/TA]TATATAATTTTATCA | 114792 |
| rs533234683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919838 | TATTTCTAGCTATAA[C/T]TGATATGCCTTTGGT | 114792 |
| rs533241800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069031 | GGGAAACAGAGAAGG[G/T]GGGGGTCTGTTGCAT | 114792 |
| rs533259500 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136194 | ATTTGGAAGTACTAA[-/T]TTTTTTTTGCCCTCA | 114792 |
| rs533271728 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963933 | ATTGTAGATGATCAC[A/G/T]GTTGAAAGAGATCTC | 114792 |
| rs533285462 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107018 | ATTTTTTGGGCTGAG[C/T]GCGGTGGCTCACACC | 114792 |
| rs533287892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136501 | TGACGAAAGTGAAGG[C/T]GTTCTTGTTTATTTA | 114792 |
| rs533291572 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026046 | AAATGAAGATCAAGA[G/T]GGGTAATATGTAAAA | 114792 |
| rs533324991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001224 | CAGCAATTTTACCAT[A/T]CTGGTGGGGCATGTT | 114792 |
| rs533339035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912419 | TTGCATCTTTAGTCA[A/G]TAAGTTTCCTCTTTT | 114792 |
| rs533369876 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057305 | TCTCCTGCCTCAGCC[G/T]CCTGTGTAGCTGGGA | 114792 |
| rs533398894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904781 | ATTGTTACAGGAATA[A/G]GCAAATAAATAGTGA | 114792 |
| rs533402570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NDUFAF4 | GRCh38.p7 | 6:96896025 | TCACTTCCTCAGAAA[C/T]CATCCTTGATCCTCC | 114792 |
| rs533415876 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103030 | TTTACCTCTACGAGG[C/T]AAATAAATATAAATA | 114792 |
| rs533416006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043380 | AAGTTCATCCATGTC[A/G]TTGCAAATGACAGGA | 114792 |
| rs533430887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915876 | TTTGCCCTCCCCCAT[C/T]GGCTTAAAAGCAGGA | 114792 |
| rs533431200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911921 | TCCTAGGCTCTTGGC[A/G]CTCCTCACTCTGCAC | 114792 |
| rs533455067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995125 | CTCTGGATGGGTTGA[G/T]ACAGAGACTTAAGTG | 114792 |
| rs533494475 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133291 | CTGGGCAAGTTGCCA[C/G]CTGGGCCTTTCAGAA | 114792 |
| rs533536339 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021714 | CAAATTTATATTTCC[A/G]AATTGGACTTCCCCT | 114792 |
| rs533537845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112073 | TTTTGGAAAAGTCAA[C/T]ATTCCAGCATGAAAC | 114792 |
| rs533539550 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047292 | GCCCTTCTTCTGGGC[A/G]CACTGTGTTTGGGAC | 114792 |
| rs533540569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091247 | GAAACAGAAAAAAGA[A/G]CATGACCATTCTAGT | 114792 |
| rs533554147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927923 | ATATCGGCTTCACAA[C/T]GACTCTATAAAGTGG | 114792 |
| rs533559931 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100225 | AATAGAGGATTCATA[C/G]TTCCCTAGTTTTTTA | 114792 |
| rs533566129 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080286 | AGGAAGGCCTGTGAG[A/T]TATGAAAAATGGCCT | 114792 |
| rs533572811 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087639 | CTGGATGGAGGGGGG[C/T]GTGCTATTTGATTAA | 114792 |
| rs533577333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062909 | ATGGTCAGGGAAGGT[A/G]TCTCAGGTAAGACGT | 114792 |
| rs533581795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015591 | TGAAATTGGAACCTA[G/T]GTTTAAAAGGGAAGG | 114792 |
| rs533582612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994588 | GCCGAAGCTTTGATG[G/T]ATCTTTTCCTTTATA | 114792 |
| rs533594002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947970 | CTTTCTGGTCTTGGC[A/G]TAAAGAAATGAATTG | 114792 |
| rs533601766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083283 | TGGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG | 114792 |
| rs533613735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913109 | TCAAGCATGGGATTT[A/G]TGGCTATGTATAATC | 114792 |
| rs533645214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035621 | TGTATACTTGGCAGT[A/T]TTTTTCTTTCAGTAT | 114792 |
| rs533672107 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007348 | AGCTTTACCAGATCA[-/T]TTCTTAAAGTGGCCA | 114792 |
| rs533688204 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050322 | ACTGATAATGCCACA[C/G/T]ACCCCAACAGGATGT | 114792 |
| rs533689682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964581 | TGGCGTGAACCCGGG[A/G]GGCGGAGCTTGCAGT | 114792 |
| rs533690953 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940682 | ACAGATAATAAGCTG[A/T]GTTACAGAAAACAGG | 114792 |
| rs533711478 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006746 | ATTTCTCCTTTGCTT[A/C]TGAAACTTAGTTTGG | 114792 |
| rs533725461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921134 | TCTTAATGATGACTA[A/G]GAATCCTCTTTATAT | 114792 |
| rs533743886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062336 | TCTCCTCCTTAGGCC[A/G]TGCCTCTTCTGCAAG | 114792 |
| rs533749073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050869 | ATAGCCAGGTGTGGC[A/G]GTGGACATCTGTAAT | 114792 |
| rs533749890 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953487 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCACAT | 114792 |
| rs533784551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978979 | ATGTCTTTTGCCCCC[C/T]TTTTTTATGGTGTTG | 114792 |
| rs533805142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948212 | TACAATGAGCGGTGT[A/G]AATTTTAGTCAGACT | 114792 |
| rs533818605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043698 | GTGCACAAAGGTTTT[C/T]CTCCACACCCTCATC | 114792 |
| rs533841050 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948886 | CTTTTTCTGACTCAT[A/G]CGAAAAAGTCATGTA | 114792 |
| rs533904476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989202 | TATTGTATCAGTGGC[C/G]TATATACATAAGTGT | 114792 |
| rs533921805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949479 | TTCTTTCCACAGATG[C/T]AGACTTGCCACCATC | 114792 |
| rs533928314 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001478 | TTTGTTTTTTTGTTT[G/T]TTTGTTTGTTTGAGA | 114792 |
| rs533963444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965146 | ATAATGGCCTGCAGT[C/T]GCATCCATATTGCTG | 114792 |
| rs533965189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078986 | CAGCTTGTATCATCA[C/T]TGGCACACAAGACAC | 114792 |
| rs533965260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070903 | TGTGTTTCATTTGAG[A/G]TATTTATTCTCCCAC | 114792 |
| rs534005946 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994418 | TACAAATTATTTATG[-/T]TTTTTTTCCTTTTAG | 114792 |
| rs534016673 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994762 | CTTTAAAAAATAACA[A/G]AAATGTTAGGCTTAA | 114792 |
| rs534017376 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955279 | GATATATATTCCTTG[A/G]TGCAAATTGAGTTTT | 114792 |
| rs534017739 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138252 | GTGCTATATAAGAAG[-/A]GAGAGGCCAGGCACA | 114792 |
| rs534027853 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003056 | TGGTAGTTCTAAGTT[C/T]TTTGAGAAATCGCCA | 114792 |
| rs534051079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136168 | AATAGTTCTGAGATT[G/T]TTCTATTAACATTTG | 114792 |
| rs534052346 | snp | A/G/T | 3.44889e-05 | 0.00415252 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113749 | TTCTTTCTTACCTTT[A/G/T]TGTCTCCTCTCATCT | 114792 |
| rs534052945 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980607 | TGTTCATCAAGGATA[C/T]TGGCCTGAATTTTCT | 114792 |
| rs534070573 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139658 | CTTAAAAATATATAT[-/AT]TCTGTACTTAATCCC | 114792 |
| rs534080990 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956796 | ACATGTACATACATA[C/T]GCCTAGCCCATATGT | 114792 |
| rs534102103 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897030 | CTCCCGGGTTCGAGA[A/G]ATTCTCCCACCTCAG | 114792 |
| rs534109386 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107378 | GAAAAATAATGGCAA[G/T]TAGATATAATTAAAA | 114792 |
| rs534113982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128487 | TGTTTGTACACACAT[C/G]CTCTTTTAAAAAATT | 114792 |
| rs534117876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137013 | GTCACTTAATTTTTT[C/T]CGGTATCAATTTTCT | 114792 |
| rs534118607 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975468 | AATGGTCATTTGCAG[C/T]CCTTTTTGTCCTAAC | 114792 |
| rs534138031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981224 | GGCTTCTTCTTACTG[A/G]TTCAATTTTGGAACT | 114792 |
| rs534139405 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973753 | TTTTAGACAGAGTCT[C/T]GCTCTGTTGCCCAGG | 114792 |
| rs534141792 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935427 | TAAAGTAAGGTAAAT[A/G]CTGTCTGTGGAACTT | 114792 |
| rs534143056 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103972 | CTCATCAACTAATTT[A/G]TTTTAAAAATGAGAG | 114792 |
| rs534150942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058071 | TATTTATGTGAGTCT[C/G]TTTCTGAGCTCTCTG | 114792 |
| rs534163324 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017403 | TCATTGGGAGAGTTG[C/T]TGCCCTTCTCTAACT | 114792 |
| rs534167064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108028 | AATTGGGTCAGGCAG[A/G]GTGCTTGAGAGACCT | 114792 |
| rs534169360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100375 | TTTGCAGCTCACTGA[C/T]AGTGTAGACCCTGGC | 114792 |
| rs534174956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974277 | TCCTTTTAGGAAAGA[G/T]TTTTCAAAGACTATC | 114792 |
| rs534176862 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981654 | TGTTAGATTGTTAAC[A/G]TGACATCTTTCTAAC | 114792 |
| rs534211068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989583 | CTGTGCGTCTTGGGG[A/G]TGGTCGTCTTGTATA | 114792 |
| rs534225805 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979825 | CTTGTTGGTATCATC[A/G]CTAATTTCAATGAGA | 114792 |
| rs534226357 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897508 | CAGTCTCAATGTCAC[C/T]GGCCTGGCGGCTCCC | 114792 |
| rs534230882 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101263 | GACAACATAGAAAGA[C/T]GATTCGTGTGCGTTT | 114792 |
| rs534271113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003665 | TTGAGTTGATTTTTT[A/G]TATATACTGTAAGGA | 114792 |
| rs534287453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985801 | CAAGGTTTTTAACTT[C/G]TTTGCCATGGGTACG | 114792 |
| rs534292958 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093891 | AAAAAAGAACCTGGA[A/G]TGCCATTATTTCTGT | 114792 |
| rs534293743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023356 | GCTGACAATCTATAA[A/G]CTGAATTTATAGATA | 114792 |
| rs534313725 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930558 | ATTCCTTCCCTCTGC[C/T]TCCCCTTTCCCCACT | 114792 |
| rs534316196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935736 | TCCAGTGACCAAATG[C/T]GCAGAATAAATAAGA | 114792 |
| rs534321145 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126200 | ACTGATTAAAATAAG[A/G]ATATTATTCATTTTA | 114792 |
| rs534352234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086646 | TTGATAAAGAAAATA[C/T]AAGGACCAAAAAAAC | 114792 |
| rs534356705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004197 | GATCTTTCACCTCCC[C/T]GGTTGGTTATATTCC | 114792 |
| rs534381394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908073 | CATTGTACTCCTGTG[A/T]ACTGGTGTTGTGCCT | 114792 |
| rs534382010 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896599 | TGCTGTCTTACACCA[C/G]TGTGCTTAAACTTTG | 114792 |
| rs534385026 | snp | C/T | 1.67722e-05 | 0.00289583 | intron-variant, synonymous-codon, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114547 | TTTATCAAAACACAC[C/T]TTCATTGTGGTATAT | 114792 |
| rs534388613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093176 | CTAACCTGGGTTATC[A/G]GGGATTTAAAAATAA | 114792 |
| rs534389408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997467 | AAAGACTTGAAGGTG[G/T]CCAGGCATGGTGGCT | 114792 |
| rs534434089 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017216 | CACATCTGGATGAGT[G/T]ATCCCATGCCATGTC | 114792 |
| rs534436015 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968959 | TTTGAGAAAGCCACA[A/G]CCACAAAAACAACAA | 114792 |
| rs534443136 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130651 | ACAGAATGTTGATCT[A/G]TTGATTGATAAACAT | 114792 |
| rs534460232 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031482 | CTGGGACTGCAGGTG[C/T]AGACCACCATGCTCA | 114792 |
| rs534463670 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921985 | CAAACTCTAGGATAC[C/T]TGTTTAAGAAAGTGA | 114792 |
| rs534465659 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065017 | GGGTTCCCTGCAGGA[A/G]CCGGGGGAGGTGTCG | 114792 |
| rs534467356 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923000 | CAATATTTAGTGAGC[C/T]GATACTATGTGGCAG | 114792 |
| rs534481165 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910286 | AACAGAAGATAAAGC[-/A]AAAAAAAAAAATTAG | 114792 |
| rs534491280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058748 | GAATGTAGACATAAT[A/G]CCTGGTGGTATGGCA | 114792 |
| rs534504323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123190 | TGAGAGCAGTTTTTC[C/T]ACACACTCTATTTTA | 114792 |
| rs534522608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010356 | GTCAGGACTTGTTCA[C/T]ATGTCTGTCTCTCCC | 114792 |
| rs534523743 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924874 | GGACGCTCGTCTTCG[C/T]TACTGCATCCCCGAA | 114792 |
| rs534525354 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067443 | TTAATGCTAATTGAT[G/T]GGGGGGTGCCTTTCT | 114792 |
| rs534549230 | snp | C/T | 6.68427e-05 | 0.00578073 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967016 | ATGCTTGCTGATTCC[C/T]CTGCACACTTCTAAG | 114792 |
| rs534569407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025504 | TCCAGTAATAGATAT[A/G]AATGCATTTCTCAGG | 114792 |
| rs534579820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032828 | TTTATAAACTAAAGG[A/T]TTTTATTTAACTGTG | 114792 |
| rs534591908 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020447 | ATGTAATTATCAAAA[A/G]TGGGCCTATTTTGTT | 114792 |
| rs534604868 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018193 | CTAAGGAGAAAAAAA[C/G]AAACAGAGAAAGCAT | 114792 |
| rs534612575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045185 | AACAGGAGAAAGAAA[A/G]GTGATGGATCACAAA | 114792 |
| rs534613589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986735 | AAAGCACAGTATTAG[A/G]GTGGGAGTGACCCGA | 114792 |
| rs534628975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938154 | TAACTTATCTGTATA[A/T]GTTTTCCTAAGTCTG | 114792 |
| rs534636024 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108990 | GAGTAACTAAATTCA[G/T]GACAGCCTGATAGGA | 114792 |
| rs534642951 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898193 | GCCCAGCATTGGATA[A/G]GACTCCACGTGATTC | 114792 |
| rs534645565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094777 | TATTGGTAAGTGGCA[C/T]GGTATTACTTATGCT | 114792 |
| rs534662474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907450 | AAGAGCTGTGAATGA[G/T]AAAAAGGTACAGATT | 114792 |
| rs534674579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950640 | TGAATGAGTGAATGG[C/T]TAGTGAACGACTAGT | 114792 |
| rs534679167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046030 | CTGGGGTTGCAATTA[C/T]TCTGTCCAAACACCA | 114792 |
| rs534687887 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072171 | TTGAGCCCCACATAC[A/G]CTGACACAGAGACCT | 114792 |
| rs534711003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942918 | CAACCTGTTCACCTC[G/T]CTCTTGCCCACATGC | 114792 |
| rs534718053 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090427 | TGGTTTTTTTGACAC[A/G]CTCCTCCTGGGCTTT | 114792 |
| rs534751583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038740 | AAAGGAAAGGAAATC[A/G]GTATATCTGCACTCC | 114792 |
| rs534768164 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946104 | TTTCATGGAAAAATA[C/T]TCACTTTACCAAAGA | 114792 |
| rs534779073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054151 | ATTAATATCAGGATA[A/G]ATAATTTGCTAAACA | 114792 |
| rs534779583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990821 | AGGTGAGCTAGACTG[A/G]CCTCTTCTCTTTAAG | 114792 |
| rs534801378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943513 | TCAGCTGTAAATCCC[A/G]CAAACTGATTTAATT | 114792 |
| rs534838802 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047117 | CTCTAAAGTGTAGCC[G/T]TCTTAAAATTGGCCT | 114792 |
| rs534850889 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139881 | GTTACTCTGACCTTG[C/G]GTCAGAACCTAACTT | 114792 |
| rs534872712 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088423 | ATTTTGCTTTCAGAT[A/G]TTAGCTCCCAATTAG | 114792 |
| rs534883019 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031002 | ACCTGCCTTCATGGA[A/G]CCTGCACTCTACCTT | 114792 |
| rs534884660 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961052 | AGGAAGGGGATTCTC[C/T]TCAGAATGTAGATTT | 114792 |
| rs534891859 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109845 | AAGAATGCCAAGAAA[-/T]TGGTTGCAGAGCAAA | 114792 |
| rs534894033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074150 | TGAAATGCATACTCC[A/G]GAGTAATGATTCCTA | 114792 |
| rs534918696 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040178 | GTTTTTTATGACTAT[A/G]AAGTTAGCTAAACTG | 114792 |
| rs534941546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116373 | TCAAGCTAGGCAGCA[A/C]ATAAGTCTTTGCTAA | 114792 |
| rs534958275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066673 | TCAAAATCATGTCGA[C/T]GTAGAAACCTTCCTT | 114792 |
| rs534977366 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141535 | CAATAATAGAAATAA[C/G]AATTCTATTAAACTA | 114792 |
| rs534991803 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036313 | GTCTATATGTGTTCA[A/G]TGATAATTTCTTAAA | 114792 |
| rs535020472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060495 | TGTGAGGTGTGGGCA[C/T]TGACTGAGGTGGCCC | 114792 |
| rs535021853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041276 | AGTACTGTATATGGT[A/G]AGGAATGCCATCCTG | 114792 |
| rs535031038 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916171 | CAGAAACAGCTGGAT[G/T]GGTTACAGGTTGGCA | 114792 |
| rs535040162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976317 | GTTCTTTCCTGGGTA[A/G]AATGCTTCCTGGGGC | 114792 |
| rs535040503 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075333 | AGTTGTCCATACATA[A/T]TTACATATTTATATA | 114792 |
| rs535049961 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012289 | AGCTGGACCCAATGT[A/T]ACCACAAAGTCCTAA | 114792 |
| rs535059995 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086373 | TCATTATTTGTGTTA[A/C]TTTAATCAGTAACTT | 114792 |
| rs535060960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082380 | GCACTTTGGGAGGCC[C/G]AGGCGGGCGGATCAT | 114792 |
| rs535069971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968139 | TTGAGAACTGGTGAC[A/G]TTGCTGTAGCAGGTG | 114792 |
| rs535076388 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008932 | CCCAGCCGCATTTTT[A/G]TAGGATAATTAATTA | 114792 |
| rs535081797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034175 | TTTAAGTCATTAATA[A/C]ATTTAAGTTAATTTT | 114792 |
| rs535091214 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065568 | GATCCTCCCACTTCC[C/G]CCACTGGTGTCACCT | 114792 |
| rs535098909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075742 | TAGTCACATAATACC[G/T]TGATTTATAACTCAG | 114792 |
| rs535103138 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117621 | CGAATTGTACAGGCT[C/T]CTGTAGCGTTTGACA | 114792 |
| rs535107186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987471 | TACAAACAAATGGAA[A/G]AACATTCCATGCTTA | 114792 |
| rs535131574 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095714 | TCATTCATTGATAAA[A/G]CTTGTGGAAGGTGCC | 114792 |
| rs535176826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998536 | CATATAAATATTTAC[A/T]ACTGTCCTAAATAGC | 114792 |
| rs535197496 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983892 | CCTTCAGTTCTGCTC[G/T]GATCTTACTTATTTC | 114792 |
| rs535214707 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933561 | AGAACTTCCTTAGTT[A/C]TTAGATGTGATTCAT | 114792 |
| rs535227085 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140639 | GAAGAATTCACTCTT[C/T]TTTCCTTGGCAGTTT | 114792 |
| rs535271825 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009114 | ATGGGGCTAATGTAG[A/G]AATTAAATAAGATAA | 114792 |
| rs535272005 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999248 | AAAAAATTAGAAAAT[C/T]AGCTGGGCATGGTCA | 114792 |
| rs535279182 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015236 | TGGACCAGTACAGGA[A/G]ATTGATACTGCAGAG | 114792 |
| rs535279681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111459 | AGGTAAACTTCACTC[A/C]CTCGAACCCGCTGCA | 114792 |
| rs535284342 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943371 | TGATATTTACTTCTA[G/T]TTCCAAGAAGAAGTA | 114792 |
| rs535289299 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969474 | TCTCTCATTTCCTGT[A/G]TTTTTGATGCATTTG | 114792 |
| rs535291297 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978303 | TTCCCCCAACCTCCA[C/T]CATTAAGTAGGCCCC | 114792 |
| rs535296627 | snp | C/T | 1.65353e-05 | 0.00287531 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132775 | AGTTCCTTTTGAAGT[C/T]TGTTCAAGTGGTTCA | 114792 |
| rs535312549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097109 | CTTTCAGTGGTGCTC[A/G]TAAGGGAGGGAAAAA | 114792 |
| rs535313516 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992319 | TCCTGGCTGTGGGGG[G/T]CCTCCCCTGGCTCTT | 114792 |
| rs535318745 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081902 | TGTTGTCATGGCTAG[A/T]GCCAAGCCAGGGTGG | 114792 |
| rs535332175 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981315 | TTCCATGAATTTATC[C/T]ATTTCTACTAAATTA | 114792 |
| rs535350592 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079012 | GACACAGCTCTTGAG[C/T]GTGACATCCCTAAGC | 114792 |
| rs535352168 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056243 | CCCTAGTAGCTGGGA[C/T]TACAGGCGCCCGCCA | 114792 |
| rs535365430 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921880 | TGATGATAGATGAAA[A/C]AAATGCTGCAGAAAC | 114792 |
| rs535367036 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033744 | AGGAGACCCCTCATT[G/T]TGGTTTTTACTTGCT | 114792 |
| rs535370775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097731 | GAAACTTTAAAAATC[C/T]GTCCTTATCACTGCC | 114792 |
| rs535372244 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125311 | TTCCAGCTCAGTTAA[A/G]GATTAGACACTAATC | 114792 |
| rs535381044 | in-del | -/CCAGA | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093068 | TGATTCATGTTGTTT[-/CCAGA]CTGATATTTTTGTTG | 114792 |
| rs535393773 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987125 | ATTAGTCTTGCTAGC[A/G]GTCTATCAATTTTGT | 114792 |
| rs535397409 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986784 | TCACCCCTTTCTTTG[A/C]CTAGGAATGGGAATT | 114792 |
| rs535402477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007463 | TCTTTGTTCCTATCC[A/T]TATTTTGAATTCTAT | 114792 |
| rs535423227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938995 | CAGGATTACTGCTCT[A/G]TGGATGTAGGGTAAT | 114792 |
| rs535424014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090763 | TCCTGTAGTACAAAA[A/G]GGAAAACTGAGGTTA | 114792 |
| rs535439920 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126019 | AAGGGGCCTAGAGTC[A/G]GGAAGCAACCTATTT | 114792 |
| rs535442797 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983512 | ATTCATCTGGTGCTG[G/T]ACTTTATTTGGTTGG | 114792 |
| rs535464903 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912032 | CATCTGCTTTATAGA[C/G]ATGTCTTCCCAGAAG | 114792 |
| rs535465260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955174 | ACCATCACATTGGAT[A/G]TAAGAGTTTGAACAC | 114792 |
| rs535484211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091355 | CTAATTCTGTTAGAT[A/G]ACATATGCCTCATTC | 114792 |
| rs535498374 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993983 | CCCTTTGCTCTACAT[A/G]GAGATACTGTATCTT | 114792 |
| rs535498604 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014947 | GGAAGGACCTGGTGG[A/G]AGGTGATTGAATCAT | 114792 |
| rs535505221 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118373 | CCAGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 114792 |
| rs535518486 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043609 | GGTTCATATGGTAAT[C/T]TTATTTTTACTTTTT | 114792 |
| rs535540696 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100466 | AGAGTCTGGCCCTGA[C/G]AGTGTTTAGTCCTGT | 114792 |
| rs535568308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118799 | CTCCAAGTCCTGTTC[C/T]GGGATAGTGCTGGAG | 114792 |
| rs535569046 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083419 | AATTGTACTTGGGGA[A/G]TAACAGAGATTCAGT | 114792 |
| rs535571399 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910710 | GTTGCATTTCCACAC[A/G]TAATCCCTTAAGCCT | 114792 |
| rs535576333 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142481 | TATATTGGCATACTA[C/T]ACTCTTGCCTGACAG | 114792 |
| rs535587663 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127615 | ATAAACTGCTTTTTG[G/T]TTCCTTTTTTTGTTT | 114792 |
| rs535600539 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952148 | TCCAGGATGGGTTCC[C/T]GCCTTTTGCCCTGAG | 114792 |
| rs535614966 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039090 | CAAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA | 114792 |
| rs535618078 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988869 | ACAAAAAACCAAACA[C/G]CGCATGTTCTCACTC | 114792 |
| rs535629325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077556 | AGTCAGGCCTCATGT[A/G]TCTGGCACCACAAGA | 114792 |
| rs535633605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020740 | CATCTCAGTCACTTC[C/T]TATTTCTTCCTTGAA | 114792 |
| rs535639755 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108766 | ATCAGAATCAGCCAT[C/T]GATTTATAGACTGTA | 114792 |
| rs535645734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927104 | CTAGATCTCTGTCTT[A/G]TATCTCAGAAAATAA | 114792 |
| rs535649854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029181 | CCAGGTCGTTGAAAC[A/G]TGGCCACATTCAAGA | 114792 |
| rs535650435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128225 | CCACCAAATCTATGT[C/T]CCTAGTGGACTCAGT | 114792 |
| rs535656119 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918721 | CTTCACATTCAGTGG[A/G]TTACTCATCAGTTTT | 114792 |
| rs535671305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007053 | TTAGCAAGGTTGGGG[A/G]AATTTTCATGAAAGA | 114792 |
| rs535712234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120586 | ATAGTCCAGAGAATC[C/T]TCCTGGAAGGAGTTC | 114792 |
| rs535715242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021902 | CCAGTTAATGCAGGC[C/T]GCAATTATCTGTGTC | 114792 |
| rs535737139 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088384 | TCACTTGCCTTTGTG[A/T]CCTGGCAAATCTCTA | 114792 |
| rs535757421 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901330 | TCCTCCTGGATGCCT[-/T]TTTTTTTTTTTTACT | 114792 |
| rs535795982 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112769 | TTTTTTAATTTTAAA[A/T]AAAAAAAGGAGAATT | 114792 |
| rs535803984 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928075 | CCTAATGCAGGTTAT[A/G]GACATGTACATAATT | 114792 |
| rs535827781 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058836 | AGGCTGGTTGCCACT[C/G]TAAGTGGCCTAATCC | 114792 |
| rs535834834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016111 | ACCTCTGCTAGGGCA[A/G]TGCAGAAGGGAAATG | 114792 |
| rs535845933 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134812 | TTCCACATCTCATAT[A/T]TTGTTAACAGTCGTG | 114792 |
| rs535851479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921188 | TAATTACGATATTCT[C/T]TCTTACAGTTAGGGG | 114792 |
| rs535858067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106674 | GCTTGAGCCTGGGAG[A/G]CAGAAGTCGTAGTGA | 114792 |
| rs535868368 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084653 | TTGACTTAAAGACCT[A/G]CTTAGTTTGAAGTTT | 114792 |
| rs535870433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057318 | CCTCCTGTGTAGCTG[A/G]GACTACAGGCACGCG | 114792 |
| rs535898011 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008884 | TGATGGGAGATGTTC[C/G]TCCTGGCTGTGCTTA | 114792 |
| rs535900323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904110 | CTTTTGGGAGCCTGG[A/G]GCAGGCAGATTACCT | 114792 |
| rs535915343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956204 | GATTCAGTTACCTCT[C/T]ACTGGGTCCTTCCCA | 114792 |
| rs535923185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947430 | AACCACATGTTAGGA[A/G]CATCGATACAATTTA | 114792 |
| rs535923351 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988265 | TCTACAAGAAAAAAA[C/T]AAACAACCCCATCCA | 114792 |
| rs535932243 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050983 | ACTCCAGCCTGGGCA[A/G]CAAGAGCAAAACTCC | 114792 |
| rs535941988 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899625 | ATCCTGGCCCAGTGC[C/T]GCTCAGGCCCTCAAA | 114792 |
| rs535958096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948030 | AGATGCCTTTCTGGA[A/G]TCCAAGGCTAGATTT | 114792 |
| rs535980284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002200 | CCTGCTCAAAGACAG[A/C]CCGGCAGAGAGAAGG | 114792 |
| rs536026783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044517 | GAATAATGCTAGTCT[C/T]ATAAAATGAATTTGA | 114792 |
| rs536041833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948939 | TACAAAACATAATGT[A/G]GAAAACTTTCTTATC | 114792 |
| rs536081218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124545 | TTGTATGTTTAATCT[A/G]TAATGGGCAGAGTCT | 114792 |
| rs536085740 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085651 | TGATAAAAATTGTTT[C/T]TTAAACAAAATATGA | 114792 |
| rs536097490 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096219 | GATTCTGAGCCAACA[A/G]CCGTCCTGTCCTCTG | 114792 |
| rs536102834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029022 | CTTTCCAGAAGACAG[A/G]AAGACTGGCAAGGAC | 114792 |
| rs536106238 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897153 | TGGTCTCGAACTCCT[A/G]ACCTCAGGTGATCTG | 114792 |
| rs536107299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112134 | TGCCAGGCTTGAGGG[A/T]GGGGCCCTCAGTGGG | 114792 |
| rs536122840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129186 | GTCTATATGCCTATT[A/C]GTGAGTGGACCAATT | 114792 |
| rs536131402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063076 | TTCAGAAAGTTCTGA[A/G]TAAAAACAGTGACAT | 114792 |
| rs536135612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070746 | CACTTTCAGTATGCA[C/T]TTTTCTTCTTAAAAA | 114792 |
| rs536143421 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079071 | GCAGACTCTAGGCAT[A/G]AGGCTGCATGTTTTT | 114792 |
| rs536144493 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985366 | TGGAGTTGCTCTTCT[C/T]GAGGAGTATCTTTGT | 114792 |
| rs536165110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934951 | CAAATTGTAGCTTGA[C/T]CTTTATTTTTGCGAG | 114792 |
| rs536181499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980053 | TTATCAGATTTAGGA[C/G]ATATGGGGCAGAGAC | 114792 |
| rs536268022 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929455 | CTGCCTATAAGACTG[A/C]TTATTATTTCAGAAT | 114792 |
| rs536278481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972397 | TGTATCCCTACAATA[A/G]AGTATTACTATTGTA | 114792 |
| rs536278903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936703 | CAGCCAAAAATTTTG[C/T]TTTAAAACCTGAATG | 114792 |
| rs536291934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107154 | AAAAATTAGCTGGGC[A/G]TGGTGGCAGGTGCCT | 114792 |
| rs536301275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099438 | ACCTGTGATTTCCCC[A/T]GATTGGACTCCTGTG | 114792 |
| rs536306239 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088497 | TTTGCATATATTTTC[A/G]GACTGATGAGCCAGG | 114792 |
| rs536308298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057930 | TGTGAAGGATTTGAG[A/G]GCTGTGTCCAGGTTC | 114792 |
| rs536313617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965255 | TTCAGTCTACCACTG[A/G]TGGGCACCTAGTTAA | 114792 |
| rs536331925 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931028 | AATTTCTAGAGCCCA[C/T]ATCTTTCTTGACAAC | 114792 |
| rs536354163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092290 | CACCGTGCCCGGCCA[A/G]TTCTCTTTCATACAT | 114792 |
| rs536356616 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013546 | CCCCACCACATACAT[A/G]CACAGACACACACAT | 114792 |
| rs536362631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100095 | AGCAGTACGCCAAGA[C/T]TGTGCCACTGTACTC | 114792 |
| rs536363890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009429 | GGCACCTAAAACTCT[A/C]TTCACTATCGACACT | 114792 |
| rs536372072 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051572 | TCATAATCCATGGTG[G/T]GCATCTGAGATTTTT | 114792 |
| rs536379259 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974584 | TCCTATATCATCACC[A/G]TCTGTCAAGTTTTTT | 114792 |
| rs536386312 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903651 | ACTTAATTTTGCCAA[C/T]GACCAAGTAAGCCTG | 114792 |
| rs536389483 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058807 | TGAGATTTGCCAAGC[A/G]GGAAAATACAAGGAG | 114792 |
| rs536400369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965873 | TTTAATAATTAAAAA[A/G]AGAAAATAAGAAATA | 114792 |
| rs536402712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002770 | TTACAGTAGTGACCT[C/G]CAGCTCCATCCATGT | 114792 |
| rs536450891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052559 | CCCAGCAGGGCATTC[C/T]GGCGTGCAGGCTGTA | 114792 |
| rs536467207 | snp | A/G | 0.000116553 | 0.00763302 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967074 | AAATGCCGTCTGAAC[A/G]CTGCCTCAGGTATGC | 114792 |
| rs536471404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975276 | AAGAAAATTATATAG[A/T]CATTCATAAATCCAG | 114792 |
| rs536475036 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971105 | CTTTATCCCACTTAG[C/T]TGTTTTTAATATGTA | 114792 |
| rs536491715 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906317 | GAAAATGAATACAGC[A/C]AGAATAAAGTTGGGG | 114792 |
| rs536492552 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995944 | ACACTAGTGAAGTCC[A/T]CCAAACTACTGTTGA | 114792 |
| rs536498828 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019121 | TATACTTGCAATTGT[-/A]AAAAAATACTCTTAA | 114792 |
| rs536507456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958983 | TTGGACCCCCACAGT[A/G]CTTATGAAAGCTGGA | 114792 |
| rs536515999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138031 | AACTTTCATTTTTTT[A/G]AAACACCAAATCCAC | 114792 |
| rs536518325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949589 | ACTGACTCACAGTGG[G/T]GAGTCCATTTGACTG | 114792 |
| rs536557068 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926790 | TCTAAAACATGACAG[-/T]TTTTTTAAGGAAAAC | 114792 |
| rs536584905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138943 | ATACTAACATAGTGT[A/T]GCATTTAGTAGGAGC | 114792 |
| rs536600151 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956414 | TTCTTCCAGAACCCA[C/T]TCTTCTTACCTGTAT | 114792 |
| rs536615643 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990253 | AATTTGAGTACATTC[A/T]GTTGCCTCTTTTCTG | 114792 |
| rs536632816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046905 | TTCAGGGTTAACATC[A/G]AGTGTATCTGCCTAT | 114792 |
| rs536635968 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055040 | TCTGCTGGTTGGCAC[A/T]GGAGAAAGTCACTGT | 114792 |
| rs536640915 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113136 | AATTACAACTGTCTT[A/C]AAGGTAAAAGTTAAT | 114792 |
| rs536685394 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024609 | TTATTTGAATCAATG[A/C/T]CAGAGAAATTGTTAA | 114792 |
| rs536689017 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998120 | CCTCCATTGAGTCTG[C/T]AAACCTCCAGTATAC | 114792 |
| rs536689991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953437 | GAGTTCAAGACCAGC[C/T]TGACCAACATGGCGA | 114792 |
| rs536698919 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137242 | AAGAAAATTTTGAAA[A/C]TAAATGAGGAGTCTT | 114792 |
| rs536705456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082384 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCATGAGG | 114792 |
| rs536729573 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991436 | CTTTGTTCCTTCCCC[A/C]ATGCAGTAAGGGTGG | 114792 |
| rs536730007 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986516 | GAGCTGTGGTGGGCT[C/G]CACCCAATTCGAGCT | 114792 |
| rs536765269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017389 | AGGGAATGCCCTCAT[C/G]ATTGGGAGAGTTGCT | 114792 |
| rs536766876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115279 | TCTTGGCCTCCCAAA[A/G]TGTTGGGATTGCAGG | 114792 |
| rs536796834 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934552 | TTCTCTACCAACCAG[G/T]TGCCCTGTCTGGGTA | 114792 |
| rs536801023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010606 | GTGTGTATGAGTGAG[A/G]AACCACAAAAGTGTT | 114792 |
| rs536839090 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108752 | GCTTACTTTATGTTA[C/T]CAGAATCAGCCATCG | 114792 |
| rs536844975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124941 | TATTTATTTTGACAC[A/G]CATCTTGACTATATA | 114792 |
| rs536853635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059605 | TATAGATGTGCAGTG[C/T]ATGAGTCAATTTAGA | 114792 |
| rs536866630 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075157 | AGAATTCCTCTGTTA[C/T]ACAGCACAAATGTAT | 114792 |
| rs536871759 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898676 | AATTTAATGAAAGGA[A/G]CAGACAATAAGACGT | 114792 |
| rs536873598 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930308 | TGAAAGTGCAAGGTA[A/G]CATGGCACAACCAGA | 114792 |
| rs536880330 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996312 | GCATCTTTTTCCGTT[A/G]GAGGCTGGGCGTGCT | 114792 |
| rs536881129 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926819 | ACAGAAGCTTCTGGA[-/T]TTTTTTTATGAGGTA | 114792 |
| rs536883127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018857 | GAAAATGATAGAATC[A/T]TAAGGAGAAATTAAC | 114792 |
| rs536885870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026929 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA | 114792 |
| rs536895519 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070776 | ATGAAGTGTTTCCAG[A/G]ATTTTATTCATGCTA | 114792 |
| rs536912428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907576 | GAAGCTCTTGAAACT[A/G]TGTTTCACTCTACTC | 114792 |
| rs536914832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053102 | CACACACACACACAC[A/G]CGCACACACATTCTC | 114792 |
| rs536942112 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974170 | TCATGGTGTTGTTGT[G/T]CAGATTACATGAACT | 114792 |
| rs536969281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019262 | CTTTTTGCAATTTGC[A/G]TTCCTTGGGAAGTAG | 114792 |
| rs536972120 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012342 | AGTCACAGTCAGAGG[A/T]GTCAGGACAGAAGCA | 114792 |
| rs537008444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013142 | TCTTAAAATAATTGT[A/G]CATTTTCTTGTGAGA | 114792 |
| rs537013272 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918344 | TGGAGAAATATTTTT[A/G]TGTTATTTTTGACAG | 114792 |
| rs537014685 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970644 | ACCTGGCACAGGCTT[A/C]ATAAATATTTGTGGG | 114792 |
| rs537033223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951522 | CTGTACCTTAACCAT[C/T]GCTGGTAAGGTAGTT | 114792 |
| rs537034771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038920 | ACATGGTGAAACCCC[A/G]CTCTACTAAAAATAC | 114792 |
| rs537040733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916624 | CTTCCATTCTTTTCT[A/G]TGAAGGCCTCTGTGC | 114792 |
| rs537044047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925555 | ATCTTATAAAGAAAG[A/G]TGACTGCAGTTTAGA | 114792 |
| rs537089021 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104047 | TTAATACTGGCTTTC[C/T]AAAGATCAGCTTACA | 114792 |
| rs537095649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039889 | AAGAGAATAATTTGA[A/G]TGTTTTAAGCATAAA | 114792 |
| rs537096798 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899595 | GCTTCCAGCATGTGT[C/T]AGCTGCTTTGCCTGA | 114792 |
| rs537114011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943567 | GAAAGCAGAAGCCCA[A/G]GGAAACAAACTGGCT | 114792 |
| rs537114609 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910241 | TTTTTAATAACCCCA[A/T]CCCCAGGGAAAAAGA | 114792 |
| rs537117738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055737 | TGGGAGGTGGAGGTT[A/G]CAGTGGGCCGATATC | 114792 |
| rs537126673 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140708 | TTTATTCATGTAACC[A/T]TTTTTTGTAATCAAA | 114792 |
| rs537146044 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948856 | AGCCAAGAAAACATA[A/C]TCCACTCTCCTCCTC | 114792 |
| rs537149765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096877 | ATATTCCTGCCCTTG[A/G]TTTTATCTTCTCATC | 114792 |
| rs537152752 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944253 | TGAATTCAAGGTATC[A/C]GAATAAAAGGCACTA | 114792 |
| rs537160582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032878 | AATTTCGGGTAATCT[C/T]CTGCAAATGCATAAA | 114792 |
| rs537178490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048554 | AGGTCTCACCATAGT[A/C]ACTTTGTTTTTTTGA | 114792 |
| rs537222745 | in-del | -/AAAAAAAA | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010144 | AAAAAAAAAAAAAAA[-/AAAAAAAA]GTGAGCATACAGAAA | 114792 |
| rs537226406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911138 | ACAGAACTTTATTCT[C/T]TCATAGTTCTGGAGG | 114792 |
| rs537235300 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094877 | CTTGTTGATGAGGAA[C/T]GCCCACTACCTTCTC | 114792 |
| rs537235662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954043 | TGGGAACTTCCTTCA[C/T]TATCACCTGAGAATT | 114792 |
| rs537238800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041366 | GACACTTTCTAGAAG[C/T]ATTTCAAAAATCAAA | 114792 |
| rs537255951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993190 | GTTAGCTTTTGCTGC[A/G]TAACAAAGTACCCGA | 114792 |
| rs537257631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982804 | ATGGGGTTTTCTAGA[C/T]ATACAATCATGTCAT | 114792 |
| rs537286027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902034 | GTGAATAGTGCTGCA[A/G]TGAACATACATGTGC | 114792 |
| rs537325280 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014846 | AATAGCTTAGTATGA[A/G]AGCAAAGGTTGTGAT | 114792 |
| rs537327925 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982074 | GTTAGGCCCATTCAG[A/T]CAAGTGTTGAGTTCA | 114792 |
| rs537360966 | in-del | -/A | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040080 | TACATTGGCAAAAGT[-/A]AAAAAAAAAATCACA | 114792 |
| rs537374404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126921 | TTGTTATATTCTATT[A/G]GACAGCACTGGCTTT | 114792 |
| rs537377037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968208 | AATCAGTGATTCTCA[A/G]TGGTGGATGGTTTTG | 114792 |
| rs537385631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060978 | CCTGCTACAAATTGC[A/G]GGAGATGTTCCTGGG | 114792 |
| rs537394885 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076653 | TATGCACAATTAGGT[A/G]TACTTATAATATTTC | 114792 |
| rs537406448 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003438 | ATTTTCTCCCATTCT[C/T]TATAGTGCCTGTTTA | 114792 |
| rs537427990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103448 | TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT | 114792 |
| rs537446038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933676 | GGAATAGCACCCACC[A/T]GTATCTCAGCTGGGA | 114792 |
| rs537452586 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052937 | TGCTGGGAAATTTCC[A/G]TTACATCTCAGGGTC | 114792 |
| rs537458841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069165 | CCAAATTCTTACTAT[C/T]CTTCACTCAGAAGCC | 114792 |
| rs537459518 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054933 | AACAGAGTGAGATCC[G/T]GTCTAAAAAAAATAT | 114792 |
| rs537479690 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020784 | TTGACTTTGTTCCAC[A/G]TTCTCCAGGTTTTCC | 114792 |
| rs537492655 | in-del | -/TGTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044831 | TCTCTTATGGTCCTT[-/TGTA]TGTCTATGATATCTG | 114792 |
| rs537498485 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006286 | GTCTTTTTAAATTGT[A/T]GTTGTTGATTTATAG | 114792 |
| rs537518824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047815 | GCCTGACAGTGAAGA[A/G]CAGAAAACATCAAGA | 114792 |
| rs537537087 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999317 | GGGAGGGTCATTTGA[A/G]CCTGGGAAGTCGAGG | 114792 |
| rs537590576 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062842 | AGAATAAAACAAAGT[A/T]AGGAGCTAGGGAATG | 114792 |
| rs537592192 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056253 | TGGGACTACAGGCGC[C/G]CGCCACCACGCCCGG | 114792 |
| rs537601946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953366 | CAAGCTTGTTGGCTC[A/G]TGCCTGTAATACCAG | 114792 |
| rs537611277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992346 | TCTTCGCCTCTCCCC[A/G]GTGGGCAGTTGTCCT | 114792 |
| rs537621976 | snp | A/T | 0.0422008 | 0.138995 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105772 | GACCAAGACAAAAAA[A/T]AAATACTTGTTACTT | 114792 |
| rs537636808 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945431 | GACCTTGTGGAGAGA[A/C]TAAAGGTGCACACAC | 114792 |
| rs537663164 | in-del | -/AC | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087690 | ATGAGAGCATGGTAA[-/AC]ACACACACACACTTA | 114792 |
| rs537670705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963233 | ATACGATCCTAGGAT[C/T]ATCAAAGGAAAAGGG | 114792 |
| rs537678161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082389 | GAGGCCGAGGCGGGC[A/G]GATCATGAGGTGAGG | 114792 |
| rs537683581 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098747 | GGTCTCACAAGATTC[C/G]TCACTGCAGTACACC | 114792 |
| rs537691760 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013336 | GCCACATTATATGAG[A/G]AAACTCACTTCAGTT | 114792 |
| rs537705947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964262 | CGAGGCATGGGAAAA[A/G]GTGCAAGGAGGTGGG | 114792 |
| rs537713006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126136 | GAAACTTTTTTTAGT[C/T]GGGCTTAATTTTATA | 114792 |
| rs537718427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050202 | TGAAAAATGTATTCC[C/T]GTTTTCCCAAATAAT | 114792 |
| rs537724591 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920470 | ATGGTACTGAGGTGA[C/T]ATGGAAGGTCCAGCA | 114792 |
| rs537729654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082605 | GGCGACAGAGCAAGA[C/T]TCCATCTCAAAAAAA | 114792 |
| rs537759509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091450 | CTACTATTGCCTGCC[A/G]TATGATGGGTGCTGG | 114792 |
| rs537772684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118390 | TTGGGAGGCCGAGGC[A/G]GGCGGATCGCCTGAG | 114792 |
| rs537781389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043143 | TTAGCCTGCAGAACC[A/G]TAAGCCAAATAAACC | 114792 |
| rs537807261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068638 | TCTTGGGCTGCTGTG[C/G]TCATTTATCAGCACA | 114792 |
| rs537809633 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988134 | AAAGAGCTTCTGCAC[A/T]GCAAAAGAAACTACC | 114792 |
| rs537817078 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030933 | TTTCTGTATTTATTG[C/T]ATGTATGCACTCCTA | 114792 |
| rs537820751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083636 | AGTCTAGAAGTATAT[A/G]TACAAAAACATTAAT | 114792 |
| rs537821063 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092213 | CCAGGATGGTCTCGA[A/T]CTCCTGACCTCGTGA | 114792 |
| rs537822344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994688 | GTACTATGAGTTCCT[A/G]TGATCATCACCATTT | 114792 |
| rs537828747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118926 | AGGGAGTGACTATTG[C/T]AGAAGGCAGGAAAGG | 114792 |
| rs537836517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948167 | GAAGTCTAGCTATTC[C/T]GTGTTACTAATGCTA | 114792 |
| rs537856731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988920 | GAGAACACATGGAGA[C/T]AGGAAGGGGAACATC | 114792 |
| rs537862333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926569 | CCCTTTCTGGATCCA[A/G]TCTCCTTGCCTTTAA | 114792 |
| rs537864491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977690 | GGTTTTGTTATTTAA[A/G]AGACAATATCAACTG | 114792 |
| rs537892175 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111493 | AACCCCTCATGGGAC[A/G]GAACATGCAGGTGAG | 114792 |
| rs537942685 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989117 | AATAAAAAAAATATT[G/T]ACATGTGTGGATTTT | 114792 |
| rs537954115 | in-del | -/TCT | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023896 | AAAGCTGCAATAGGC[-/TCT]TCTTCTTGTCTTGTC | 114792 |
| rs537957137 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976889 | CAGACACACACCACC[A/G]CGGCCAGCCTATATA | 114792 |
| rs537960417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105251 | GAAGATAAAGAGCAT[G/T]CTCGATACTCTGTTT | 114792 |
| rs537963981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014750 | AACTCATAAAGGATG[C/T]AGCCAAGTCTCAAAT | 114792 |
| rs537977939 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985402 | TCTCTGTATTTCCTG[A/G]ATGTGAATGTTGGCC | 114792 |
| rs537989691 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119765 | ATACATTTAGGGAGA[G/T]AATGTGTTGTTTTTA | 114792 |
| rs537990309 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977932 | AGTTCCATTAATATA[A/T]TTATACATTTCACAC | 114792 |
| rs537995887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007550 | CTGGTTGAAGGTAGG[A/T]AGACCCTCTGGTTTT | 114792 |
| rs538013349 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003027 | TGTACCCAATAATGT[A/G]ATTGCGGGTCAAATG | 114792 |
| rs538015912 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070866 | TACTTGGAAATTGGT[A/G]GGGGGTGTGTAAAAG | 114792 |
| rs538019013 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978992 | CCTTTTTTTATGGTG[G/T]TGTTTATTTTTTGCT | 114792 |
| rs538032369 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975217 | AGAGTGAAGGGGTAA[A/G]TTTCACAATGTGTGA | 114792 |
| rs538043224 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912043 | TAGAGATGTCTTCCC[A/T]GAAGTCCTACAGGCC | 114792 |
| rs538048731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920031 | CAGTGGAAAGGCAGG[A/G]TCTATTTACACAGGA | 114792 |
| rs538050151 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089330 | ATAGTGTTGGGAGCT[A/G]GATTCTGGGGTAAAA | 114792 |
| rs538088548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016195 | GTGAGAAGAGGGCCA[C/T]CATCCTCCAGACCCC | 114792 |
| rs538103387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106705 | GCTGAGATTGCGCCA[C/T]TGCACTCCACTCCGG | 114792 |
| rs538105453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113666 | AGTTATACTGTTTGT[A/C]AGAAAGTTTGTATTA | 114792 |
| rs538106454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912677 | CTTAGGACTTAAACT[C/G]AAACATACAAGGTAC | 114792 |
| rs538130982 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984217 | CTTAATCCTGAGTTC[C/T]AGTTTGATTGCACTG | 114792 |
| rs538171332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008975 | AGTTTTAGACTGAGA[C/T]CAGTCTAATTTATAA | 114792 |
| rs538225938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035854 | CTTTGGGGTTAATCA[A/G]TCTGGATGTCCACTT | 114792 |
| rs538229245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043586 | TATTACCCAGAAGTG[G/T]AATTGCTGGTTCATA | 114792 |
| rs538235761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100213 | TTACAAAGTAGAAAT[A/G]GAGGATTCATAGTTC | 114792 |
| rs538243636 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897054 | ACCTCAGCCTCCCGA[C/T]AAGCTGAGGCTACAG | 114792 |
| rs538245724 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995251 | CTGCCTAGGTGTTAC[A/G]GTGAAGGAAGTTCAG | 114792 |
| rs538263755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051843 | ACATGAACTTTTTCT[C/T]TTATTGAGAAAAAAA | 114792 |
| rs538282574 | in-del | -/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999214 | AGCCTATGCGACATA[-/G]GGGACACCCCATCTC | 114792 |
| rs538289127 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896920 | TAAACGCTTAACACA[A/T]ACGCTTTCTTTTATT | 114792 |
| rs538296107 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002892 | CATTTCCTTTATTTA[A/G]TCTACTGTTAATGGG | 114792 |
| rs538310752 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040534 | GCTGGGCCCTGCTTG[G/T]AGTATCAGTTTCAGT | 114792 |
| rs538311569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948786 | CACCTCCCCAATGCA[A/G]TTCTCTCTCAGATTT | 114792 |
| rs538311864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029235 | GATAAACCATAATGA[C/T]GCTTGTTTTGAAGAG | 114792 |
| rs538312120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036241 | GTATTACATAAAATT[C/T]ACATTTCTCTAACTT | 114792 |
| rs538320512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137305 | CACTGAAAGAAAATA[C/T]ATCAATTAACAAGAG | 114792 |
| rs538335667 | in-del | -/GCTT | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025309 | TTGACTGCATTCTGG[-/GCTT]GCATGCCTGAACTCC | 114792 |
| rs538346325 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941591 | ATGACCAAAAAACAA[C/T]CAAGGTAAGACTAGA | 114792 |
| rs538350846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029956 | ATGTAATGGATCTAC[C/T]GTAATCATTGCGAGT | 114792 |
| rs538352951 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934662 | TAGGCGGATTGCTGC[A/C]GAGAGCAGCTAATAT | 114792 |
| rs538357812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949768 | TCTCTCTTTTTTTCC[C/T]CTCCTAAATTTTAAT | 114792 |
| rs538385747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138072 | TGTTTAAATAGTTAG[A/G]GAAAAGTCAAATGAA | 114792 |
| rs538390087 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037063 | CATTATGAATGTTAG[C/G]TTTTTAATATATCAA | 114792 |
| rs538423034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121118 | GTTGCACTTTGTTGA[C/T]TTACCCTCACATCAC | 114792 |
| rs538427876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989894 | TGTTAAAAAAAAGTG[C/T]GATTATTATTATGAA | 114792 |
| rs538428817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037847 | CAATGGAATAGAATA[G/T]GGAACCCAAATATAA | 114792 |
| rs538433314 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123197 | AGTTTTTCTACACAC[A/T]CTATTTTATGAGCAC | 114792 |
| rs538444306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942538 | TAATTTGAAAGTATA[C/T]GAATGATAGAAGCTA | 114792 |
| rs538455082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928466 | GGAGGGGATGGAGGA[A/G]GACAAATTTGGGAAG | 114792 |
| rs538455808 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071465 | AGCTCTGCATGGGCA[A/C]CCTTCCCTTCTGCTC | 114792 |
| rs538456720 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129775 | TAATCCCAGCTACTC[A/G]GGAGGATGAGGCAGA | 114792 |
| rs538458256 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942213 | AGCCCAAGATCTGCT[A/G]GCCCCACTTGTCTGG | 114792 |
| rs538461306 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063860 | CCTCCTTGCACCTGG[A/C]AGTAATTCATGTGAA | 114792 |
| rs538464348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023266 | TTTGAAGGCATAGGA[C/T]TGGTTAGCAAAAGAT | 114792 |
| rs538472387 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961162 | CCTTCTTTATCTGCC[A/G]TGTGATATTATGCCA | 114792 |
| rs538522001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122179 | TGGGTCACAAGTTTG[C/T]ACCTATTTGCTCTAA | 114792 |
| rs538522509 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997114 | AAGGCTTGAGGTCTG[C/G]AGAGTGTTGGGAAAA | 114792 |
| rs538522938 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064550 | CAATTTAAATATACT[A/T]TGGTATATCTACATA | 114792 |
| rs538522953 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057369 | TTGTATTTTTAGTAG[A/C]GACGGGGTTTCACTG | 114792 |
| rs538549884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016566 | TTTTGATTTTACAGG[C/T]TTATAGGTGGAAGGG | 114792 |
| rs538553631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032109 | CAAGATAAATTGCCC[A/G]CATGACTAGTAGTTT | 114792 |
| rs538572264 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973588 | ATTTCAAACATTTCT[A/T]ACTGCTGTGTCATGT | 114792 |
| rs538579838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965319 | TTTGTAGTATATAGC[A/G]GATTATGATTCAACA | 114792 |
| rs538597737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930159 | TGCTTCAGTGAGAAC[A/G]TATTTGATGCTAATG | 114792 |
| rs538610822 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129421 | TACTTTCTTTACTTA[C/T]CTGTCCATTACTTAG | 114792 |
| rs538616657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966084 | TACAAATCATCAGAA[A/G]TAGGCACAGCTTAAC | 114792 |
| rs538617535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065403 | TGTCTGAGGCAATAT[A/G]GCTGGTAGGACGTTC | 114792 |
| rs538652222 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063704 | TGAAACTTACTGATT[C/G]AGTATGTCTGGGAGG | 114792 |
| rs538652781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017458 | TTCCATTCTGGAGAG[C/G]GACTGATGGAACAGA | 114792 |
| rs538686194 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015899 | GCCATGGCTAAAAGG[A/G]ACCAAGGTACAGCTC | 114792 |
| rs538694249 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052336 | CAGGTGGCATGTGAC[A/G]TGATTTTCCAAAATA | 114792 |
| rs538756998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045113 | TGAGGCAACTCTGGC[A/C]GCTAGAAGAAAATAG | 114792 |
| rs538786033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958868 | GCAGAAGGCATGCAG[A/G]TGCACACACAGCTTG | 114792 |
| rs538791317 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053106 | CACACACACACACGC[A/G]CACACATTCTCTCCT | 114792 |
| rs538804595 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022272 | CAACTCTCAACCTCC[A/G]TCCATTCCAGTCACA | 114792 |
| rs538809064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086626 | CTTCAATATTCCACA[C/G]TGTCTTGATAAAGAA | 114792 |
| rs538812575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950498 | TTTATCAGTTGTCAC[A/G]TTAAAAAAAAAAAAC | 114792 |
| rs538822400 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998870 | CATGGTAAACTGATC[A/G]TTATTTTCCATCAAA | 114792 |
| rs538836679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968008 | GAGCAAAGAATAAGA[A/G]AGATGACAAACCTGG | 114792 |
| rs538899852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942864 | GAGAATCACTCCTTA[C/T]GGCAGAATGGCTTTC | 114792 |
| rs538910797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960289 | ACTAGCATTTTCCCT[A/G]TTCTTACTGAACAAT | 114792 |
| rs538914171 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997627 | ATGCACCTGCAGTCT[C/T]AGTTTCTTGAGAGGC | 114792 |
| rs538945535 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979882 | CTCTTTTACCTTTCC[A/G]GATAGCTGTGTTCTT | 114792 |
| rs538949979 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914119 | TCTACAAGCAAAAAA[-/G]GGTGGATGACCTCTA | 114792 |
| rs538950001 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952226 | GGGTAAATAATTATC[A/T]TACTTGTTTTTATTA | 114792 |
| rs538954396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088335 | GAGACTAAAACTGAA[C/G]AAATCAGCTGAAATG | 114792 |
| rs538963910 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986348 | GGAGGCAGTCTGTCC[A/G]TTCTTAGATGTCCAA | 114792 |
| rs538963959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981422 | TTTCATTTCTGATTG[C/T]ATTTATTTGGATTTT | 114792 |
| rs539020110 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025307 | TGTTGACTGCATTCT[A/G]GGCTTGCATGCCTGA | 114792 |
| rs539028196 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038137 | TGGGATTAAGACCCC[A/C]AAAACACAGGCAACT | 114792 |
| rs539056860 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018132 | AAAAAGAGTACAGTA[A/C]GTATAATTAATATTG | 114792 |
| rs539061323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124346 | TCTCATTTCTAAACA[C/T]TGTCATTTGAGTGAA | 114792 |
| rs539071994 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992251 | CCCAGGGTTGCAAAG[C/G]TCCATGGCAGAAGTG | 114792 |
| rs539088131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945295 | CATGATGCCACATAA[C/T]TCAAAACCATGCTTC | 114792 |
| rs539094048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074562 | GGTCTCACTCTTATT[C/T]GTAATAATGATTAAG | 114792 |
| rs539144267 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987076 | TTTATCATTTTTTAT[C/T]GCATCTATTTCATTC | 114792 |
| rs539149309 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923989 | GGTATGGTTCTGTGG[C/T]TGTTGTCTGTTTGCG | 114792 |
| rs539156330 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986568 | ACTCAAGCCTTGGCA[A/T]TGGCGGGCGCCCCTC | 114792 |
| rs539158300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011482 | ATAATAAAAGGAAAT[C/T]TGTGCCTTTTTGCAT | 114792 |
| rs539165746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967561 | TTTGGGGAGTACAAT[A/G]CTTATTCTCAAAATG | 114792 |
| rs539171634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938916 | GATATTCTAAAGTGA[A/G]CTGCAGGGGCCCAGG | 114792 |
| rs539174872 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983388 | ATCAGGATGATGCTG[G/T]CCTCATAAAACGAGT | 114792 |
| rs539218102 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988892 | TCTCACTCACAGGTG[G/T]GAATTGAACAATGAG | 114792 |
| rs539232697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110379 | TGTCACTCATTAAGA[G/T]ATGCAATTCATGACG | 114792 |
| rs539237752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908401 | GCCTAATGATTTGGC[A/G]GGATTCATTTGTGAG | 114792 |
| rs539247689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118341 | TTGTAGACAAAGGCC[A/G]GGTGCAGTGGCTCAC | 114792 |
| rs539256924 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976572 | TATGTATTGTTTCGG[-/AT]ATATATATATATATT | 114792 |
| rs539262336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095569 | TTTCGACCCCATGTG[C/T]AGTCAGTATCCTGAA | 114792 |
| rs539275333 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990478 | ATTTCAGCTGTGCTC[C/T]CTCTTAGTGCTCTGA | 114792 |
| rs539279303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068357 | ACCAAAGTACTGAAT[A/G]CGCAACTCCCTTTTT | 114792 |
| rs539282964 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965365 | TGATTTAGTGAGTTG[C/G]TCTCCAAACGATAAA | 114792 |
| rs539287607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019842 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 114792 |
| rs539288036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047016 | AATTGTTGCTGTCTT[A/G]GAGAGAAATTGGAAG | 114792 |
| rs539288348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005417 | CTCTCTTATTTATTC[C/T]TTCAAAAAGCAAACT | 114792 |
| rs539289642 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955599 | TCAATCTGCCACTTT[C/T]AACTTTTGGTAAGTG | 114792 |
| rs539302801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909062 | ATCTAAGCAGCAGAA[A/G]GGCTAAGATGCTACC | 114792 |
| rs539303042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977605 | CCCAGTAAAGCCTAA[A/G]TGTTACAGACACCAA | 114792 |
| rs539351293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039992 | TTATCATATGTACCC[C/T]TGAAATATGTACATT | 114792 |
| rs539359536 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138851 | TCTTAAATGAAGTAA[C/T]GCTACCTACCTCATA | 114792 |
| rs539362715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006388 | CCATTTCTTTACTTT[C/G]AGCCTATCGGGGTTA | 114792 |
| rs539364969 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962665 | TATTCTATAATAAAA[G/T]AAGACACACAATGAT | 114792 |
| rs539366479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104210 | GATTGAGCAAAGGGA[C/G]AACTCAGGTCACTTT | 114792 |
| rs539376790 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076292 | TTACCCGCTCAGTGA[A/G]TATGGACTATGCAAA | 114792 |
| rs539391936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991560 | CAGGCCAGGGCAGGG[C/T]GGTTGTGCTAGGCGC | 114792 |
| rs539407984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006945 | TTCATATCTACCTTA[C/T]GGAATCTGAGGACTA | 114792 |
| rs539420688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033073 | TTACCACAAAATATA[A/G]ATTTTACTAAGAGCT | 114792 |
| rs539420860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900436 | AATAATTTAATTTTT[A/T]AAAAATAAAAAATGC | 114792 |
| rs539437543 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017988 | GAAGTCACTGGGAAT[A/T]TGGGTTTTATCTATT | 114792 |
| rs539444428 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914211 | GCTGACATCCTGATA[C/T]TAGCCCAGTGAGACC | 114792 |
| rs539445003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938323 | ATCAGGATCAGACTT[C/T]AGTTCCACTAGGTTC | 114792 |
| rs539447311 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973685 | ATAGGGACTTACATG[G/T]TTTTTTCCCCTTAAG | 114792 |
| rs539452167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911255 | CTTCCACTTTCCTGA[C/T]AGAAAATCTTGACGT | 114792 |
| rs539492581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097576 | CTTGGGATTTAATTT[A/T]TTCTGTGCCCTGAGG | 114792 |
| rs539496057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000159 | CAGGAGGTTGACATA[C/T]TCTGCAGAAGACTGA | 114792 |
| rs539508649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026340 | TCATGTCACTGTACC[C/G]TAGCCTGGGTGACAA | 114792 |
| rs539510575 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956543 | AGCTTTCTCCTTTCT[C/T]TCCATCCTTTAGTGC | 114792 |
| rs539511359 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130504 | ATGTAATTCAAAATG[A/C]ACTATAAAATGCAAC | 114792 |
| rs539521311 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142973 | GGATAGGTAAAGATA[C/T]ACAAGTTTTAAACTA | 114792 |
| rs539521798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133909 | CAAAAACCAGTCATG[C/T]ACTAGGGTTAGGGTT | 114792 |
| rs539531036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000782 | AAAATGTGAAGCAAC[A/G]AAGATGTTACTCAGT | 114792 |
| rs539541725 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117511 | GAAATCTTGAAACCT[G/T]TTTATAGTTTTTAAA | 114792 |
| rs539556001 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135389 | TGGCTCACTGCAACT[G/T]CTGCCTCCTGGGTTC | 114792 |
| rs539585406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034441 | ATTTTGAAATCAGGA[A/G]GTGTGATGCCTCCAG | 114792 |
| rs539590392 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962885 | GTGTTTTATTTTTGT[G/T]TGCAAGCTGGATTTA | 114792 |
| rs539611059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019291 | AGACTCTGAGACAGA[A/G]ATTAGTGTGAAGAGC | 114792 |
| rs539620034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993828 | ACAGGATGACATGAA[A/G]AGGGCCAGCTTGTGA | 114792 |
| rs539634725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977064 | TGTGGTAATAAGATT[A/G]CTGTTTTTCTTGAAG | 114792 |
| rs539643672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932892 | CCAATTTTTGATTTC[C/T]GTGTTTCATGCTGTT | 114792 |
| rs539644917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127001 | TAGAGTACGGATGTT[A/T]GAGCTTTAAAATTGA | 114792 |
| rs539657219 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988209 | AATCTACTCATCTGA[C/T]AAAGGGCTAATATCC | 114792 |
| rs539665831 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108532 | GTTAGATGAGGTTCA[-/T]CAGCACAGAGGTGAT | 114792 |
| rs539668295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061120 | TTCCACCACCTGGAG[G/T]TCAGGCGGGGAAAGA | 114792 |
| rs539670615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968695 | TCTCAGACTCTCCCA[C/G]TGTGCCATGTGGAAG | 114792 |
| rs539692302 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917541 | CTATGACAGAGGCAC[A/C]ATTTCTTGTTCAATA | 114792 |
| rs539731740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054980 | TGATTCCAGCTTGTG[A/G]CATCTTTGGAGAATT | 114792 |
| rs539750691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021024 | TAATGTATTAGAGTC[C/T]TCCAGAGAAGCAGAA | 114792 |
| rs539758959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934230 | TTTCGAAAATATAGA[C/T]TACTGGATCTTCTAT | 114792 |
| rs539802071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096959 | TTAGGTCATTGGAAG[C/G]CTTTTTAGTCATTTT | 114792 |
| rs539805657 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910386 | ATATGATGGAGGAAA[G/T]AAGGGCTTGCTCCCT | 114792 |
| rs539822947 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126882 | AAAATTTATCATTGC[A/T]TATGTGGCTTGCATA | 114792 |
| rs539824262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961970 | AGCACCGTTACTACC[A/G]TGACCCATAGTCAGA | 114792 |
| rs539829658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002005 | AGATAACTCTACTGT[A/G]AAGAACTGGCTTACA | 114792 |
| rs539831174 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141892 | ACTTCTTAGATCCTT[A/G]AAAACAAAATAGCAA | 114792 |
| rs539859456 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957392 | AAAATAATTACATAT[A/G]TGTAGAATGTTCATT | 114792 |
| rs539863128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962459 | TGGAGAGCTTGGAGA[C/T]GGGGGTCTGAGTCTT | 114792 |
| rs539865881 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090158 | TCTATTAATAATAAA[A/T]AAAAACAACAATGTA | 114792 |
| rs539866439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056266 | GCCCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 114792 |
| rs539866539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048998 | AGGCCCTGAGGCACC[G/T]CCACTGTGCCTTGCA | 114792 |
| rs539880527 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003356 | GGTTATTTGTTTTTT[G/T]CTTGTTAATTTAAGT | 114792 |
| rs539893823 | snp | A/C | 3.3e-05 | 0.00406189 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041576 | GGCTTAAAGCAGGCT[A/C]TGGAGTTTGCATACA | 114792 |
| rs539903851 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954100 | CCTTGGTCTCCTGAA[C/T]CACATGTCTTCCTTT | 114792 |
| rs539905766 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093935 | ACTGTGTGGGAAAAA[G/T]TCTGTAGGCTGTTGT | 114792 |
| rs539921904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935537 | ACTAACTGTGAAACC[A/G]CGTCTATCATCAATT | 114792 |
| rs539923876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946725 | TTGCCAATCCTGCTC[C/T]AACTAGACCTAAGGT | 114792 |
| rs539935210 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084531 | ATCCATCTTAGGTGG[A/T]TTCAATATAGAATTA | 114792 |
| rs539953716 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982684 | TGGTTCTCTGTTTGT[C/G]TGTTACTGGTGCATA | 114792 |
| rs539957587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091004 | TGAGGCAGGCTGATC[A/G]CTTGAGCCCAGAAGT | 114792 |
| rs539967735 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065440 | CAAAGACCATTTCTT[C/G]GTTGGATGAAAACTT | 114792 |
| rs539982243 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955497 | GTTATTTCCTCAAGA[A/G]AAAGATGAAAAAAAT | 114792 |
| rs539997250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987664 | ATCCTAAGCCAAAAG[A/G]ACAAAGCTGGAGGCA | 114792 |
| rs540008001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082672 | TTTGGACTTTGGACA[C/T]GATGAGTTTATGACT | 114792 |
| rs540019254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947711 | TGCTCTTTGCATTGT[C/T]CTTAGTAATTATATT | 114792 |
| rs540043267 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095310 | GAGTGAAGCCCCATA[A/T]AAATCCAATAAAGTG | 114792 |
| rs540065781 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077097 | CACAGCTGGAGAGAG[A/G]AGAGTCAAACAAATG | 114792 |
| rs540073584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076726 | ACGTATGCTAAAAGT[A/G]GCACACAGTTCTGAA | 114792 |
| rs540093595 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988644 | ATGCTGCTATAAAGA[C/T]ACATGCACACGTATG | 114792 |
| rs540099039 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037844 | GATCAATGGAATAGA[A/T]TAGGGAACCCAAATA | 114792 |
| rs540122162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069218 | GGAGGGAGAAAGGGT[C/G]CTGCCCTAAATCTCC | 114792 |
| rs540131960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077452 | TCATCACTAAAAACC[A/G]AGAGAAGTAAGCTTC | 114792 |
| rs540142552 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026713 | GTTATTAAGAGAGGA[C/T]ATTAAAAATAAGAGA | 114792 |
| rs540162887 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984875 | TAGCCCATTTACATT[G/T]AAGGTTAATATTGTT | 114792 |
| rs540194601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120006 | GGATGCAAGTGCACC[A/G]AGCATATATATTAAT | 114792 |
| rs540215751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105345 | CTACTTCTTGTTGCC[C/T]AAGAGCTCATCAACA | 114792 |
| rs540216678 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965514 | GGATTTTTGCTCTCC[A/G]TTCAGTTGTTGGGAG | 114792 |
| rs540227813 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977198 | CCTCACAACAACCCA[C/T]TGTGCACATATATAT | 114792 |
| rs540267345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112452 | TTTTCATTGATGATT[C/T]TTTTTTTTTCCTGAG | 114792 |
| rs540271303 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980529 | CTTGATTGTGGTGGA[C/T]TAGCTTTTTGATGTG | 114792 |
| rs540274348 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936751 | CTAAAACTGCAGCAG[C/T]TTCCATCCCAAGAAC | 114792 |
| rs540301120 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902492 | GCGTTGCATATTGGA[C/T]CTTTGTCAGATGCAT | 114792 |
| rs540316857 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961154 | TTTGATTTCCTTCTT[G/T]ATCTGCCATGTGATA | 114792 |
| rs540317706 | in-del | -/TTGTGGAT | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004886 | TTTATTAGTATTTTG[-/TTGTGGAT]TTTTGCATCTATGTT | 114792 |
| rs540324375 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956006 | GATGTTTATTGGACT[C/T]ACAGTTCCATGTCAT | 114792 |
| rs540353984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972771 | TTGATATATGTTCTA[C/G]ATGCTGAGGGAGCTG | 114792 |
| rs540364364 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902120 | TAATGGGATTGTGGG[C/T]TTGGATAGTATTTCT | 114792 |
| rs540368856 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971814 | AGCATATCTATAATT[A/T]AAAATTTCAGGTAGC | 114792 |
| rs540373733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134878 | AAAAACTTCGTAGTC[A/G]CATCATTTGTTTTTT | 114792 |
| rs540376913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008546 | ACTCTCTGAGCTGTG[C/T]ACTGGCTGGAGTCCT | 114792 |
| rs540383358 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940885 | CAATAATACACCCAT[A/C]ATTGTGATGTAGGCA | 114792 |
| rs540406477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964764 | TATAGGGAATAATAA[A/G]TAGTAAATAATATGT | 114792 |
| rs540414641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903302 | ATACTTACTCTCATT[C/T]CCTTGTGTGACATGC | 114792 |
| rs540419462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001858 | TTGTTAAAGGTTGTT[G/T]CCGTTCATCTAGACG | 114792 |
| rs540465604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913119 | GATTTGTGGCTATGT[A/G]TAATCTTGCTAAGAT | 114792 |
| rs540467442 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970853 | CTATAGAAATGAAAT[G/T]ATTTTATTATAGGGT | 114792 |
| rs540473460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035899 | GAATGTTTTTGGTAA[C/T]TATTCCTTTTCAATA | 114792 |
| rs540477780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904817 | CAGATGTGATTATGT[A/G]CAGGGCAACATTTAA | 114792 |
| rs540484815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028827 | CCATCCCTAAACATC[C/T]GAAAGAGGCAAATTT | 114792 |
| rs540494096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119170 | GCTCTACCTGTGGGA[A/G]GAGGACAATTAGCAG | 114792 |
| rs540502935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127917 | TTTCATCTAACAGCT[A/G]GGGGTTGAATATGCA | 114792 |
| rs540510871 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092517 | CAAATGTGATGAGGG[A/T]ATCTCCATTTCCTTC | 114792 |
| rs540512456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069645 | TGCCTTATACCCTCC[C/G]TCCCTTCACATCGTG | 114792 |
| rs540521181 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042829 | TGTTTGTCCTCTCCA[A/C]ATCTCATGTTGAAAT | 114792 |
| rs540524747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940898 | ATAATTGTGATGTAG[A/G]CATAAGGTAAGCATC | 114792 |
| rs540525395 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912102 | TCATCATCTTCCCCC[A/G]ACAAACCTGCTCTTT | 114792 |
| rs540575368 | snp | C/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085206 | GGAGAAGGCAGTGAT[C/G]GATTTCTTAGTGAAA | 114792 |
| rs540579303 | in-del | -/CTCA | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926932 | CATAATTACTGATGT[-/CTCA]CTCAATTATAAGTTA | 114792 |
| rs540582283 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963650 | TCCCTTCCTCCTTCC[C/T]GGGTTCATTAAGCTG | 114792 |
| rs540596004 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036527 | GGAAGACTTTCACCT[A/G]AGATGTGATGATACC | 114792 |
| rs540597638 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940274 | TGATTGAGATTGAAA[C/T]TGCCTAGGGATAGAA | 114792 |
| rs540605796 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897287 | TAGGAAAATACTTTA[A/G]ATGGAAATCAAAATT | 114792 |
| rs540634745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129335 | TTTCTTGGCAAAAAG[C/G]AATCTGGGTTCTTCC | 114792 |
| rs540653177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928249 | TTGATGGCTGGGTAT[A/G]ATTATATTAAATGAA | 114792 |
| rs540656739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906606 | ATGTGGGAGGTTAAG[C/T]TTTTTGGTCCAATTT | 114792 |
| rs540670288 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897888 | CCGGAGCATGCGCAC[A/C]AGTGAGGGGAAGCCC | 114792 |
| rs540679038 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113150 | TCAAGGTAAAAGTTA[A/T]TTGAGAGAAAAAATT | 114792 |
| rs540689692 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091936 | TCCTCAAACAAAATT[A/G]TAATTTTTCATCATG | 114792 |
| rs540696537 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121645 | GTTTTGTTTTGTTTT[G/T]TTTTTTTTAATGTCC | 114792 |
| rs540717568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985700 | TTGTCACGTAGTTCT[C/T]GTGCCTTGGTTTTCA | 114792 |
| rs540766916 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023814 | CTAATGTGGTAACTG[A/T]GGTCTCTCTTCTCTT | 114792 |
| rs540769277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050549 | GATGTAAGGCAAGCA[A/G]GAAAATAGGGAAAGG | 114792 |
| rs540782030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057550 | CTCAGATCTTTTACA[C/T]CCCCCTCCCGCCCCC | 114792 |
| rs540785144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929721 | TTGCAATGCATTAAT[A/G]TATTTAATTTAACTT | 114792 |
| rs540803409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024800 | ATAGTTTTAAAGTAA[C/T]AATAATAGCTAACAT | 114792 |
| rs540804852 | snp | A/G | 1.64746e-05 | 0.00287002 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114068 | GAGGTCTGCAAGGTC[A/G]AGGAACTTCGGTACT | 114792 |
| rs540805379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016926 | CTGTCTCCTGCTGCC[A/G]TGTGAAGAAGTCCTT | 114792 |
| rs540808778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009025 | TCTGGCTGTGTATAT[C/T]CTTGGGCAAGTGGCT | 114792 |
| rs540819495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064996 | TCAACTCAGTGACCA[C/T]GCACAGGGTTCCCTG | 114792 |
| rs540833222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913609 | GCAGTCTAGATGGGT[C/T]GGTAGGGAGACTAGG | 114792 |
| rs540853040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051126 | AAGGTGCCTGAGGTC[A/G]TATGTACAGATCATG | 114792 |
| rs540858181 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031935 | CAACCTGGATTATAG[C/T]GACAGTTTCTATATA | 114792 |
| rs540879365 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009796 | TTTAAAAAGCACGTG[A/G]GGGTCTTCTTAATCT | 114792 |
| rs540891292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017597 | ATCTTGAAGTTGTGA[C/T]AGACAAGCCAGACTA | 114792 |
| rs540896431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905864 | ACTATACATATTTAA[A/G]AGAACCATTTAGCTG | 114792 |
| rs540914622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043964 | ATTGCTTTAACTATT[C/T]GAGTTCTCAGTTGTA | 114792 |
| rs540960854 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923338 | GCTTTCATATTCGAT[A/T]TTCTGATAGAAGACA | 114792 |
| rs540967101 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052700 | TCCCCGCAAATTTCC[G/T]AATTTCCCTGAGAAG | 114792 |
| rs540969410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949137 | GTTTGTCTATTTACT[C/G]TTTATTCTTCTTAGA | 114792 |
| rs540995938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078591 | TTAACCTTGAGAGGA[G/T]TTTATTATCTTTAAC | 114792 |
| rs541006203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949857 | GGTTTGCCACTAATA[A/G]CTGGAATTAAATTTA | 114792 |
| rs541028651 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105270 | GATACTCTGTTTAGA[A/G]AGGAAAAGATTCGTC | 114792 |
| rs541072124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030896 | GATGAGTTTTGAAGA[C/T]GATATTGGTTGATTC | 114792 |
| rs541085720 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950995 | CAAATTACTCAGTTT[A/G]AACAAAAAAAAAGTA | 114792 |
| rs541089135 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967611 | ATAATTCATTTATTT[A/C]ATAGATATTAATTAA | 114792 |
| rs541096197 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077394 | TTTGATAATGTCTGA[-/T]TTTTTTTTTTGGCAA | 114792 |
| rs541097217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004851 | AGTGCATTAGCTTTT[C/T]GATGTGCTGCTGGGT | 114792 |
| rs541125838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959721 | GGAGACACTAGCATG[A/C]GGTGGTTGCAGGTTC | 114792 |
| rs541128028 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038395 | GATATACAGATGTCC[A/G]ATAGATATATTTAAA | 114792 |
| rs541171548 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943350 | CACAAGACCTGTGCG[G/T]TAATATGATATTTAC | 114792 |
| rs541180370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072785 | CAATCTACTCAGTTG[A/G]AATTATATCTTCCTC | 114792 |
| rs541200475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980939 | AACTTACAATCATGG[C/T]AGAAGGGGAAGCAAA | 114792 |
| rs541210931 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047131 | CTTCTTAAAATTGGC[C/T]TACAGATTTCATCCA | 114792 |
| rs541238671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065437 | TTCCAAAGACCATTT[C/T]TTGGTTGGATGAAAA | 114792 |
| rs541239537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981530 | TGATCTTTTATATGA[C/T]TTTTAGAATCTCAAT | 114792 |
| rs541252270 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96899922 | TGAATATCTTAAGAT[A/G]CTAATAAACCCAGGG | 114792 |
| rs541253264 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073830 | TGGCTTTCCTTCCAG[A/C]GGAAGGAAAGGAGTG | 114792 |
| rs541271333 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034069 | GCTTTTGTTGCCAGT[A/G]GTTTGGTGTCTTATC | 114792 |
| rs541274155 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024381 | GTGAACATGAAGAAG[C/T]ATGTGGGTTTTTGTT | 114792 |
| rs541283144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108352 | AGCCACCAGTTCCAA[A/G]AATAATTTTTTTCAA | 114792 |
| rs541313094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066261 | ACAGTTTGGTTAGAG[C/T]GTTAGTTATCATGAT | 114792 |
| rs541313513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033135 | GTATACTTAATAGAC[C/G]GCAGTATAGTGTCAA | 114792 |
| rs541319007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074578 | GTAATAATGATTAAG[A/T]CAGTCTGTAGGTAAG | 114792 |
| rs541338091 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137014 | TCACTTAATTTTTTC[C/G]GGTATCAATTTTCTT | 114792 |
| rs541380137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067279 | TCTCTTTCATTTCCT[C/T]TGGCAGGCTGCTGAG | 114792 |
| rs541417712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932535 | GTTTCCCTTCTCTCA[A/C]CTTGTACTGTTTCAC | 114792 |
| rs541423365 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907711 | ACTTAACTCGCCCAG[C/T]TCATTTCTGTATCAA | 114792 |
| rs541434194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982971 | GCCAGTTTTCAAGGG[A/G]ATGCTTCCAGTTTTT | 114792 |
| rs541436925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976551 | AAAATTTAAAAGTCT[A/T]TAAGTATATGTATTG | 114792 |
| rs541453484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963114 | ACCAAAGACAGATTA[A/G]CAAGAGAAAAACAAA | 114792 |
| rs541486058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103299 | GCTCACTGCAAGCTC[C/T]GCTTCCCAGGTTCAT | 114792 |
| rs541489855 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027173 | CTCAAAAAAAAAAAA[-/T]AAAAGAAAAAGAAAA | 114792 |
| rs541495066 | snp | A/G | 1.68843e-05 | 0.00290549 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139308 | CATCATGAACAGGAG[A/G]AAAACATAGCTCTGA | 114792 |
| rs541517557 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087749 | TAATGTCATCTGGGA[C/T]CATCCCATATTTGGT | 114792 |
| rs541521173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977142 | CACTTCTTGTGATTC[A/G]CATGGTGAGCAAAGG | 114792 |
| rs541531969 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102216 | TCAGATTTACCTCTA[C/T]AGGCATATACCAATT | 114792 |
| rs541536400 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061218 | CATCAAAACCTGTTT[G/T]CAAATCTGGAGAAGC | 114792 |
| rs541539442 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039213 | TTTAGCCATAAAAAA[A/G]TGAAATCCTGTCATT | 114792 |
| rs541549878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103575 | AAATTTGAAATTTGT[A/G]TTCTTTGGCACAAAT | 114792 |
| rs541562280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968757 | CATCTCCTTGTCCTG[A/G]AAAGCTCTGTTTGCC | 114792 |
| rs541579783 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131099 | GGTGTGTATCATTTA[A/T]GTTCTAACAGAACTG | 114792 |
| rs541599383 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985535 | AGATTTGGTCTTTTC[A/T]TATAGTCCCATATTT | 114792 |
| rs541614463 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007605 | GGTTCTTTCTCATGT[A/G]TATGGGCTGATGTTT | 114792 |
| rs541616821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999047 | TTTAAGGAGGCATCT[A/G]ATAGGCAGATTAACA | 114792 |
| rs541651222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006430 | ATGGGCCTCTTGAAG[C/T]GAGCATACAGTTGGG | 114792 |
| rs541651606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999418 | ACAACAACAAAGAGT[C/T]AATTTCCGTTTTTGT | 114792 |
| rs541652795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132096 | GATTATCCAGGCTGG[A/T]CCCAGCTCAGGAACT | 114792 |
| rs541656341 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951798 | AAGAGTCAAATAATC[C/T]ACAAGGCTTGTTATG | 114792 |
| rs541656539 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986577 | TTGGCAATGGCGGGC[A/G]CCCCTCCCCCAGCCT | 114792 |
| rs541667163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910528 | ACTTGCCTCCACATA[A/T]CTACAGCACTTCATA | 114792 |
| rs541683490 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052017 | CCTTAATATAAAAAG[A/G]CCACCTTTACTATCC | 114792 |
| rs541684667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991670 | GCTCTGCCTTAGTGC[C/G]TGATCACTGCGTTCC | 114792 |
| rs541694288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982525 | TCTCTGCCTTTTAAT[G/T]GGGGCATTTAGTTCA | 114792 |
| rs541715780 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953543 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCTGGGA | 114792 |
| rs541717354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124526 | CTACATTCTAATCCA[C/T]TGGTTGTATGTTTAA | 114792 |
| rs541719325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025826 | ATGAGGTAATAGTAG[C/T]ACCTGACTTCACAGA | 114792 |
| rs541731952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901742 | CTCCTCCCACCCTCC[A/G]ACCTCCAACAGGCTC | 114792 |
| rs541752677 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057584 | TCAAAAAATCAGATG[A/G]TTCATTTTTTTCATT | 114792 |
| rs541760460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090185 | TGTAGAGTTTCCATA[G/T]TAAAATGTATTGAAT | 114792 |
| rs541775462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993379 | AAGGGAAGCTGGGCC[A/G]TGTATTTAGAAACTA | 114792 |
| rs541799515 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134005 | AAGTTAGAACTTAAC[A/C]AAAAAAAACCCCTAC | 114792 |
| rs541805156 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943867 | ATAATTACTGAAAAG[A/G]AGGTTGTTGGAGGTA | 114792 |
| rs541806721 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109864 | TTGCAGAGCAAAGCA[A/G]TATCAGCTAGAATTA | 114792 |
| rs541811742 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936005 | GTATCCCAACATTGA[C/T]TGGGCCTTTTCTCAG | 114792 |
| rs541818759 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099613 | TGAGACTATCAGGCG[A/G]CTGGTTCTCCACCAC | 114792 |
| rs541823446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018959 | ATGTAGACGGAAGAT[A/G]TGGATAGTACACATT | 114792 |
| rs541858510 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065985 | AGTAAATGGTTAATG[-/AT]TTTTTTTTACCTTAT | 114792 |
| rs541899681 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987754 | TGGTACCAAAACAGA[C/G]ATATAGACCAATGGA | 114792 |
| rs541911585 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019358 | GGCAGGAAGGAGAAG[A/T]TGGTCTTCAATGCAA | 114792 |
| rs541912763 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005840 | GACTGTGCTCTGAGA[A/G]TGTGGTTGGTATATT | 114792 |
| rs541939689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960793 | TGGTCCAGAAGGGTA[C/T]GACAGCTGGAAGCGG | 114792 |
| rs541947273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119089 | CAATAATTATCTTGT[C/T]CTCTGGGAAACATGC | 114792 |
| rs541964685 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947688 | AACTAACACTTTCAC[A/G]GATTTTATGCTCTTT | 114792 |
| rs541975422 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999908 | GCAAGGGCTCCTAAA[A/C]CATCACCACTACAGC | 114792 |
| rs541985067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047367 | TCCTTGCACAGCCAT[G/T]CATGGAGGCCATTAT | 114792 |
| rs542004828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909723 | CCAGTCCAACATTTG[A/G]GAGCTAACCAGAAAA | 114792 |
| rs542016717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014258 | CGAAATCGCGCCACT[A/G]CACTCCAACCTGGGT | 114792 |
| rs542036970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918931 | AAGAGCCATCTCTCC[A/G]CCTGTGCAGTATAGC | 114792 |
| rs542046993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111664 | GCCATCTGTGGATGG[C/T]TTAAATATTAACAGC | 114792 |
| rs542053327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014910 | TCTCGAATTTTAATC[C/T]CCATAATCCCCATTT | 114792 |
| rs542077208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062442 | GGAGTTGGCGAAAGA[C/T]GGGTTTCTCTTTCTG | 114792 |
| rs542078765 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914854 | GTTCCCTGTTCCCGG[A/G]AGGTGACCATATTAA | 114792 |
| rs542158375 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908451 | TGAATGTTATTAACA[G/T]GGTTCTGCCACATGC | 114792 |
| rs542162122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987292 | CTCTAGTTCTTTTAA[C/T]TGTGATGTTAGGGTG | 114792 |
| rs542189270 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945690 | CACTTAAAATTTTGG[C/T]CATTGTAGGAAATGG | 114792 |
| rs542191024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027786 | GACTCAGGCCTTCTG[C/T]CCAGCCTACAAAACT | 114792 |
| rs542192978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902314 | GGTGTGGGATGCTAT[C/T]TCATTGTGGTTTTGA | 114792 |
| rs542219812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042537 | TATATACTTATGTGA[C/T]GTAAATGTGATGTTC | 114792 |
| rs542230620 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108971 | TAATAAATACAGCTT[C/T]GTAGAGTAACTAAAT | 114792 |
| rs542244379 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056246 | TAGTAGCTGGGACTA[A/C]AGGCGCCCGCCACCA | 114792 |
| rs542277045 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947764 | ATGCTGTGAGGTAAG[C/T]AGTATTATATTAATC | 114792 |
| rs542281200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043305 | ATTCAGCATATAAGT[A/G]AGATCATGAAGTATT | 114792 |
| rs542282440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955602 | ATCTGCCACTTTTAA[C/T]TTTTGGTAAGTGTAT | 114792 |
| rs542337064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111377 | GGCCTCCAGATTCCC[C/T]GACCCCTTCACGGGC | 114792 |
| rs542345150 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074924 | TTGGCAATCTCCTTA[C/T]GTGCTGAGTCAGGTT | 114792 |
| rs542365411 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061862 | TTCCCTGGAAAAATA[G/T]ATTCGAACAGTCAGT | 114792 |
| rs542381752 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984447 | CCTTGTTAACTGTCT[C/T]ATTGATCTGTCTAAT | 114792 |
| rs542395963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941093 | CTTAGCCATTATTTC[C/T]TCCTTTGTACTTTTG | 114792 |
| rs542398128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104719 | AAGGAAAATGTTGAC[A/G]CAGTTTTAATTATAG | 114792 |
| rs542399634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036386 | GGATCATTACTGGAA[A/G]TTATCATATTCCTTT | 114792 |
| rs542401096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128012 | AAAAGAAATATTTTT[A/G]TTCTCTTTTCCATAT | 114792 |
| rs542404247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934246 | TACTGGATCTTCTAT[A/G]CTTACTGTGTGAGAA | 114792 |
| rs542405177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035995 | GATATTGTTCCATAA[A/C]ATCCATAGGCTTTCT | 114792 |
| rs542413648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977864 | GAAATAAAAAGTAGG[A/G]ATTTAATTCTAAACT | 114792 |
| rs542423289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077834 | CTCTGTTGCAATCTA[C/T]GAGAAAGACATTATG | 114792 |
| rs542449344 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983646 | TTTATCCATTTCTTC[C/T]AGATTTTCTAGTTTA | 114792 |
| rs542502311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071010 | TTATTCCATCAGTTA[C/T]GCCCTGTGTTTCCTC | 114792 |
| rs542530933 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073208 | GCCTACTTCAAATTG[A/G]CAACCTATTGGACAA | 114792 |
| rs542532642 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939304 | GGCACACAGTTACTG[A/G]GCATCTGTCAAGTGT | 114792 |
| rs542533315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105890 | CACTTGTATTTATAT[A/G]TATTTGCAAGATATA | 114792 |
| rs542539890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979584 | TGTGACTTCAAACTA[C/T]ACTACAAACAATACT | 114792 |
| rs542547761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056521 | TTGCTTGCTCCTCCC[C/T]ACTCTGTAGGCTTCA | 114792 |
| rs542567463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064181 | TGGTCTTATATGGCA[A/G]GGAGAAACATATGCC | 114792 |
| rs542600276 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925467 | CACTATATGGTATGC[-/T]TTTAAAAAGGATTCG | 114792 |
| rs542632041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964625 | CCCACTGCAGTCCAG[C/T]CTGGGCGACAGAGCG | 114792 |
| rs542632744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091092 | GCATTGTGGCATGCA[C/G]CTGTAGTTCCAGCTA | 114792 |
| rs542637821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001554 | CTCACCAAAGCCTCA[A/G]TCTCCCAGACCTGAG | 114792 |
| rs542656431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083195 | AGGAGTTCAAGACCA[A/G]CCTGACCAATATGGT | 114792 |
| rs542678847 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904549 | GATGCAAAGTCTGAA[C/T]AGTGTAAAAATGTCA | 114792 |
| rs542682168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091629 | TGCCAAGTTGGGGCA[C/T]GTTGAAATGATATGG | 114792 |
| rs542687785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009063 | ATTAAGTTTTATATT[A/C]TTCTCCAATTGTAAA | 114792 |
| rs542689979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994359 | TTCTAATATTTTATA[A/G]TTCCATTTATATTTC | 114792 |
| rs542690671 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141599 | CAAATATACATTTTC[A/G]ATTTAAGTGAACTAC | 114792 |
| rs542707905 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099744 | CTGCTGCTTTGATTC[C/G]TTACATGCTTGATTT | 114792 |
| rs542745770 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966414 | TGACAACTGCATCCT[C/G]TTATATATTTCAATC | 114792 |
| rs542769624 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014273 | GCACTCCAACCTGGG[C/G/T]GACAGAGCGAGACTC | 114792 |
| rs542773586 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002533 | TTATATAGGTAAATT[G/T]TGCGTCATAGGAGTT | 114792 |
| rs542780621 | in-del | -/AAAACA | 0.0596104 | 0.162024 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138530 | GCAAGACCCTGTCTC[-/AAAACA]AAAACAAAAACAAAA | 114792 |
| rs542785527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922098 | TTGACCTGGCACCCA[A/G]TTTCCTATAGTGAAT | 114792 |
| rs542789827 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957966 | ATACATTGTACTTTT[A/C]CTTTATCTGCTTTGG | 114792 |
| rs542791527 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896345 | CCACAAAATCCAACA[A/G]CACCACTTACTAAAG | 114792 |
| rs542813695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128531 | GTTTACGGTGGGTAC[G/T]GGCAAACATCACATC | 114792 |
| rs542830985 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016446 | TTGGATTTCAGACTT[A/G]CATGGAACTGTAGCT | 114792 |
| rs542843676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120178 | AGGAACTGGGCAGGG[G/T]TTAGGTCTTGAACAT | 114792 |
| rs542846487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997109 | GACCAAAGGCTTGAG[A/G]TCTGGAGAGTGTTGG | 114792 |
| rs542867395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137755 | TAGCCAGGATGGTCT[C/T]GATCTCCTGGGCTCG | 114792 |
| rs542891225 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985549 | CATATAGTCCCATAT[A/T]TCTTGGAGGCTTTGT | 114792 |
| rs542910889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120758 | CCTGGTAGAGGTTAG[G/T]AGGTGGATAACTTGG | 114792 |
| rs542915974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935404 | TATTGAGTTACCTTT[C/T]CCCCCCATAAAGTAA | 114792 |
| rs542916627 | in-del | -/AG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079874 | TTTTAGAAAAAAAAA[-/AG]AGTAAGATTTTCTTT | 114792 |
| rs542920190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022937 | GCATAAGGCGAAGAG[A/G]AGGCAAGCACTTTCT | 114792 |
| rs542926772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129476 | TTTGGTCTTCATTTA[A/G]TTTTACAATGAGAGC | 114792 |
| rs542939133 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923041 | AGGGCCAGGAGATAC[C/T]CTGAGACACTCAGCT | 114792 |
| rs542962814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928825 | TTTCTAGTAGAGTCA[C/T]AGACTTGGAGGCTAA | 114792 |
| rs542963507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079253 | ACCGCAAAGGCCATG[G/T]CCACTCTGCTGCAGA | 114792 |
| rs542968323 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113254 | GGGGGAGTCTTTTTT[C/T]TTTCTAAATCATTCT | 114792 |
| rs542977970 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054375 | TACTTAATGAACACC[C/T]ACTATATGCTAAGGA | 114792 |
| rs542986457 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118468 | TACTAAAAATACAAA[A/C]ATTAGCTGGGCGTGG | 114792 |
| rs542998162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030957 | ACTCCTAGAATCTGG[C/G]AGCACCACAGTGAGA | 114792 |
| rs543013796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122613 | AATTAAATTGTAAGC[A/G]TGAAGTTATAGTCTT | 114792 |
| rs543018746 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985933 | AGCTGTGTCCTTTGG[A/C]GGAGGAGAGGTGCTC | 114792 |
| rs543019971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986224 | TGCTGCCGGATCGTT[C/T]CTCTGGAATTTTTGT | 114792 |
| rs543022569 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919614 | CTGTGATGCTTATTA[-/T]TTTCCAATAATGCAA | 114792 |
| rs543028989 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898357 | AGTTGCCCTTTCCTG[C/T]TTTTGTGAAAGGAAA | 114792 |
| rs543041899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016332 | AGGGGTGGCTGCCCA[A/G]GGCTATGGGAGCCCA | 114792 |
| rs543060039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921414 | TGAATAGGATGAATT[A/C]GCTACAAAATGTACC | 114792 |
| rs543061014 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107453 | TGCTAATTCATTGTA[C/T]GACTTGGGTTAAGTC | 114792 |
| rs543080390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016743 | TGGTTTGGGCTGTGT[C/T]CCCAGCCAAATCTCA | 114792 |
| rs543110310 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992620 | CGTGCGCGCATGTGA[A/G]TGCAAGAGACCATTT | 114792 |
| rs543120355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100506 | TATGGGTTCCCCCAT[A/G]CCAGTCTCTGTGCCC | 114792 |
| rs543142118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073634 | TGGATTCCTTCTGCA[C/T]GTACCATAAGAGCTC | 114792 |
| rs543166703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003142 | ATTCCCTTTTCTCTG[C/T]AACCTTGCCAGCATC | 114792 |
| rs543173768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913753 | ATATTGCCAGGCTTT[C/T]CCTTAACATATGTGC | 114792 |
| rs543206253 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942425 | ATTAGCTCTACCATG[C/T]AATAATTTCCCTTGT | 114792 |
| rs543207606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011112 | AGCGTTTGGACATGA[C/G]GGAATTATCATGTAT | 114792 |
| rs543211885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018299 | CAAAGGCATCTGTTG[A/G]AAGATACAAACTAAG | 114792 |
| rs543223003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982450 | TGGGGGTCATTGCAT[C/G]TGAGATGGGTCTCTT | 114792 |
| rs543229789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958555 | GTAAAACACAAGGCT[A/G]GTAGTGTTGGAAGGG | 114792 |
| rs543244713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011629 | TGTAGTGTGAAAAAT[A/G]GATACATATTCAGAG | 114792 |
| rs543250152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996139 | CACTCTGTAGGTTCT[A/G]GAAGCTGTTGTCTAA | 114792 |
| rs543268444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949984 | TGCCTTATCTTGCTG[C/T]TCAGTTACTCTGTAA | 114792 |
| rs543270459 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897909 | GGGGAAGCCCCGCCG[C/T]GGGCGCTTAAATGCG | 114792 |
| rs543273539 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97139029 | GATGGTGACATAACT[A/G]AATTTAAGTTCAGAA | 114792 |
| rs543283224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138328 | AGGATTGCTTGAGCC[C/T]AGGAGTTTGAGAGCA | 114792 |
| rs543310255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045322 | TTTTGTGTTTTTTGG[C/T]TTACAGATGTGAAGA | 114792 |
| rs543340091 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038364 | AATGGGCAAAAATAG[A/G]TATTTCTTAAAAGAA | 114792 |
| rs543340678 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082475 | AAAATTAGCCGGGCA[C/T]GGTGGCGGGCGCCTG | 114792 |
| rs543342705 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100892 | AATGAAGCTTCAAAC[C/T]CCCAGGCCTAGGTGA | 114792 |
| rs543362683 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139495 | TATGTATGACTTTTA[C/T]TGTGGTATAGCTTAG | 114792 |
| rs543366204 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030376 | TTAGGACTCAATTTG[C/T]ATCACTTCTGTGTGA | 114792 |
| rs543389581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038136 | TTGGGATTAAGACCC[A/C]AAAAACACAGGCAAC | 114792 |
| rs543389776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942709 | TCAGAATATCCCTTC[A/G]GGGTCATATTTGATT | 114792 |
| rs543417694 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039305 | GACAAATATTGTTAA[G/T]TTGTCACTCATATGT | 114792 |
| rs543425747 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139980 | ATTATGAGGATTAGG[C/T]GAACACTTTGTAATA | 114792 |
| rs543428484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942937 | TTGCCCACATGCCAC[A/G]GTTAAAAATTAAATT | 114792 |
| rs543437372 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922594 | GACAACTAAAAGACC[C/T]ACATGGATTATACCA | 114792 |
| rs543479014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040279 | TTTCTTAAGTCAAAG[A/G]TTAAAGGTGCACAAA | 114792 |
| rs543497846 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981776 | CATTATTTTTAAATA[A/T]TTTTTTGACTTCTAC | 114792 |
| rs543502899 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054112 | GAAAGCAACATGATA[A/G]CAAAAATATATGGTC | 114792 |
| rs543512606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952585 | CTCCCTAAAACTGAC[A/G]CTTCCTTGTTCAGGG | 114792 |
| rs543515894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937021 | CTCAATTCATCTTAC[C/G]CTGTATTTTTTTCCC | 114792 |
| rs543519648 | in-del | -/AAT | 0.00159617 | 0.0282053 | cds-indel, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898993 | AAGATAATCGAATAG[-/AAT]AATAATAATAAAACA | 114792 |
| rs543554787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033214 | GTATTATGATATTTG[C/G]TTTATTAAGTTGGTC | 114792 |
| rs543555411 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923406 | TTAGGATGACACTGC[A/C]CCTAATGTTTGTAGT | 114792 |
| rs543564117 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119241 | GTGGCACTCTCAGCC[-/CT]CTCTATCCCCTACTG | 114792 |
| rs543575577 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013935 | TAAACTGAAAAATTA[A/T]CATAAGTGCAGTGGT | 114792 |
| rs543579104 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979494 | TCTGTTCCATTTGTC[C/T]ATGTGCCTGTTTTTA | 114792 |
| rs543590638 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132861 | AGAGGCTTAACGTCC[C/T]GTTTTTTGTGCAACT | 114792 |
| rs543593407 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033797 | TGAGCATCTTTTTAT[A/G]TACCTGTTGCCCATT | 114792 |
| rs543595161 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066109 | GGTTATAAGACTTCA[A/C]AAGTGTGTGTTTGAC | 114792 |
| rs543638453 | in-del | -/AATATATTTACTGTAAGA | 0.0221141 | 0.102801 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907062 | TTGATAAGTGGTCTT[-/AATATATTTACTGTAAGA]AATTATAAGTATTTA | 114792 |
| rs543651655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967321 | ATTTTTTAATCTTTT[C/T]TTCTTATTTAGGATG | 114792 |
| rs543654651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102552 | AGTCTCATGTCATCA[A/G]TCCAGTATTGAGTAA | 114792 |
| rs543655656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125499 | TACAGTCTGAAATCA[A/G]TTCTATTAAGCAAAG | 114792 |
| rs543657928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059910 | ATACAGGAAAAAAAA[A/C]ATACCAAAGAAACAA | 114792 |
| rs543662973 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052570 | ATTCCGGCGTGCAGG[C/G]TGTAGGTCAGTCCTC | 114792 |
| rs543685078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932574 | CAATTTCCCCCCCCC[C/T]CTTTTTTTTTTTGAG | 114792 |
| rs543704519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068072 | GATGCACAATGCCAT[A/G]AGATCAGGAATATTG | 114792 |
| rs543729961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027378 | ATTACCAATATCAGA[C/T]TGGGCAGGTAAGAAA | 114792 |
| rs543732127 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105609 | AGAGCTATCTGCAAC[C/G]AGATTTTACATAGGA | 114792 |
| rs543745545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933147 | TTTATCTGTGCAGGA[A/G]CATCACCCCAACATA | 114792 |
| rs543750533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983543 | TAAGCTATTAATTGT[A/T]GCCTCAATTTCAGAG | 114792 |
| rs543754564 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095068 | ATTCTACGTGAATTA[C/T]AATGTAATTTGGCAT | 114792 |
| rs543758195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997836 | TACAAACCATAAAAA[A/C]CGTACAAACCAACCA | 114792 |
| rs543774967 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959927 | TTGGTCTCTTTAGCA[C/T]TTCAGGGTATGACTG | 114792 |
| rs543800603 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900005 | GTTCACTGTTCAACA[C/G]ATTGAACAGCTAGTA | 114792 |
| rs543814375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925930 | GCTTACTAGAGCTTA[C/T]ATGAAAGTGCAGTGG | 114792 |
| rs543815445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095815 | GATGGATTTGGAAAA[C/T]ACATGTGTTTGAACC | 114792 |
| rs543820164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969028 | CCTCTTCCTAACTGT[A/G]GTCGGGGTCATTGTC | 114792 |
| rs543826125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061707 | TAGTTGTTCTCCATA[A/C]ACCTGTGTGTTTGAG | 114792 |
| rs543858347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969672 | CCTTTCCCACAACTA[A/G]GCCAAAACCTGCCTC | 114792 |
| rs543861279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960398 | TGATTATCCTAAGAT[C/T]GTATGTAAGGCCAAG | 114792 |
| rs543877011 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132289 | CTAAAAAGCATTTGC[A/G]GGTATAGAAGAGGTG | 114792 |
| rs543878579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917710 | TCTCTGTGTGCCAGG[A/G]ATCAATTCCTGTGAC | 114792 |
| rs543883637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991160 | TTTGTTCCTTCCCCA[A/G]TGCAAGGGCAGCAAG | 114792 |
| rs543892931 | in-del | -/T | 0.02016 | 0.0983543 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947741 | TGACTCATTAAACTC[-/T]TATAAACATGCTGTG | 114792 |
| rs543906548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081457 | ATTGGCTAGCCCTGG[C/G]AGGGGCAGTCTATTC | 114792 |
| rs543918069 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991788 | AAAGTGCAGAGCTGC[C/T]ACCGCGGAGAGCCCT | 114792 |
| rs543923408 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134014 | CTTAACAAAAAAAAA[A/C]CCCTACATAACTGGA | 114792 |
| rs543935037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124573 | TCTGATACATACAGT[A/G]GTGTAAGTATTTTCA | 114792 |
| rs543944008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962169 | ATTTATTTTGTCTGT[A/G]TAAATATATTTTCAG | 114792 |
| rs543948311 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120978 | AACAAACAGAAATGT[A/C]GTATTCTACAATGCT | 114792 |
| rs543952894 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987475 | AACAAATGGAAGAAC[A/G]TTCCATGCTTATGGG | 114792 |
| rs544001104 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983044 | CTCTTATTGTTTTGA[C/G]ATACGTCCCATCAAT | 114792 |
| rs544002839 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986944 | TGGAAATGCAGAAAT[C/T]ACCTGTCTTCTGCAT | 114792 |
| rs544009808 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125255 | TGATTGGCCTGGATA[G/T]GTTCCTTCCCCTTTA | 114792 |
| rs544021133 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048901 | TGTTTCTCTCAGGAG[A/T]AGTGTTAAGACTATT | 114792 |
| rs544035990 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117050 | TCGCCAGTGACATTT[C/T]TAATACCTTCAGTCA | 114792 |
| rs544038576 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000404 | CATTTTTTGACAGGA[A/C]GTCTTTCTTGAGGAA | 114792 |
| rs544054835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954408 | TAAAGAGAAAAAAAA[A/C]TGGCTGGAAGCTCTG | 114792 |
| rs544074750 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966499 | TCTCTCTCTATGTTA[-/T]TTTTTTCCACCTACT | 114792 |
| rs544084711 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976585 | CGGATATATATATAT[A/T]TTTTTGTTTTGTTTT | 114792 |
| rs544086108 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987800 | CAGAAATAATGCGGC[A/G]TATCTACAACCATCT | 114792 |
| rs544111081 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083083 | ACCCTATGAGCTTGT[G/T]GAGCTCTTAAATTTG | 114792 |
| rs544138513 | snp | C/T | 0.000802729 | 0.020018 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946949 | CTATATACTTATTAA[C/T]AGTGGGCACATATTT | 114792 |
| rs544157945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110629 | CCTCTTCCCTCCCTC[A/G]GTACATTTCCCCTGA | 114792 |
| rs544168432 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971744 | CAGGTGGAAAAAAAC[A/G]GAGGGACATATATCC | 114792 |
| rs544172404 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988593 | ATTTGACCCAGCCAT[C/G]CCATTACTGGGTATA | 114792 |
| rs544176700 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101510 | GACACTTAAGAAAAC[A/G]AGAAGTGTTTGTAAT | 114792 |
| rs544211502 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094640 | ATTTTGATATTCTGG[-/T]TAGAGAAAGCATAAC | 114792 |
| rs544216021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055487 | CTCCTCTACTGCATT[C/G]TATTGCTCACCTTTA | 114792 |
| rs544220405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111159 | ACTTTATTCTGGTCC[C/T]ACATGGTGGCTAAGC | 114792 |
| rs544220866 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997602 | AAAAAATTAGCTGGG[-/T]TGTAGTGGCATGCAC | 114792 |
| rs544222377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013511 | TTTTACTAAGAAAGT[C/T]CCTGAAGTCACCCTG | 114792 |
| rs544237056 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999983 | ATGGGGAGGGAAAGA[A/G]AGCAGGAAAAGAATG | 114792 |
| rs544240146 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898547 | ATTTTAGTTATACTT[C/T]CCCTTATCTTATTTT | 114792 |
| rs544243697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974919 | TTTTACTCAGCTTTG[A/C]GATGGATCTGCTGGC | 114792 |
| rs544262067 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006607 | CTCTATATACTTAAA[A/T]GTGTTTTTGTGGTGA | 114792 |
| rs544262905 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028797 | AAATGTATTCAATAA[G/T]AAAGCGTAAAAGTGC | 114792 |
| rs544307620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015100 | GGTCCTTGCTTGCCC[C/T]TTGCCTTCTGCCATG | 114792 |
| rs544310627 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107198 | CTCGGGAGGCTGAGG[C/T]AGGAGAATGGCGTGA | 114792 |
| rs544318303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999843 | TTATCTCAATTTCAT[A/G]GACATTTACCGAGCG | 114792 |
| rs544320471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918794 | TAAAATACCAATTCT[C/G]ATTCCACTGGAAATG | 114792 |
| rs544334575 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953792 | TCTAAATGTTATTTA[C/T]ATAATCAAACCATGA | 114792 |
| rs544348031 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007106 | GTTGCTTGTTTTTTT[C/T]TCTCTCTCTTTTAGG | 114792 |
| rs544349697 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910777 | TTAATCTGGATTACC[A/G]TGAAGCAATTAGATT | 114792 |
| rs544350907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021360 | GAGACCCAGGAGAGC[C/T]GATGATGTAGTTTCT | 114792 |
| rs544371650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978590 | TGCTATTGTGAATAG[C/T]GCTACAGTGAACATA | 114792 |
| rs544394947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106028 | CATTCCTTTGGGGTC[A/T]TAGTGTATAATATAT | 114792 |
| rs544396773 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057667 | GATGTATCTGTTGCA[A/G]ATATTTTCTCTTAGC | 114792 |
| rs544412885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901770 | CTCCAGTGTTTGTTG[C/T]TCCCCCTCCATGTGT | 114792 |
| rs544415223 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046533 | ATGAGGGCTTAGACT[A/T]GTTCTCCCTATGTGA | 114792 |
| rs544417363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912378 | TCGTGCTTTCTCTGT[A/C]GCTTCCATATTTCAT | 114792 |
| rs544418259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927436 | CAGCACCCTGGTATA[C/T]AAAATGTTTACTCCT | 114792 |
| rs544438775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008433 | ACAAGGAAGACCACC[C/G]TGCTGTGTCCAGGTA | 114792 |
| rs544459378 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060508 | CACTGACTGAGGTGG[C/T]CCACGTCATCATGCT | 114792 |
| rs544468613 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092149 | CATGTGCCACACACC[C/T]GGCTAATTTTTTTGT | 114792 |
| rs544472654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126480 | AGAAACTTAGCTGGA[A/G]GTGTGATGATTTTTT | 114792 |
| rs544475115 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034643 | CAATCCATGGACATG[G/T]ATGTCTTTCCATTTT | 114792 |
| rs544478600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994089 | AACATCCTTGAAAAG[A/G]AAGTTCAGAACAAAA | 114792 |
| rs544507013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076282 | TTTCTTCCCTTTACC[C/T]GCTCAGTGAGTATGG | 114792 |
| rs544530765 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048257 | CAATTATGTCATATC[C/T]GGGCTTCTGAAGAAG | 114792 |
| rs544531402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935550 | CCGCGTCTATCATCA[A/G]TTGATTTTGAACTTG | 114792 |
| rs544531884 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063427 | GGGGAGAATTGCAGG[C/T]AGAAGGGGTTGGGAT | 114792 |
| rs544533256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099109 | CCTGACTGAGTTCTG[A/C]GTTTCCCCACGTCTG | 114792 |
| rs544542144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947539 | CAATGTCTTACAAGC[A/G]TCTTTACAGGGTTAT | 114792 |
| rs544546094 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939161 | TGTCATTGCAGGATG[A/C]AAGTTAGAAAATACT | 114792 |
| rs544551301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135787 | GCTCCATTTTTTTAT[A/G]TTATGGATGACGATA | 114792 |
| rs544603792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940230 | GTGTTTGGAGGTCAT[A/G]GAAAACATTGGACCC | 114792 |
| rs544606236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905604 | AAAATGGAAATATAA[C/G]AATACTACTTATTTC | 114792 |
| rs544622518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036077 | AACGACCAGTATTCA[A/G]GTTTACTAATTCTTT | 114792 |
| rs544637760 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995008 | AATGTTTGTGGGGTT[A/T]CTCATCTTCTTCACT | 114792 |
| rs544649387 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103702 | CTGCATTGGCCCCAC[A/G]TGCATGTGCACTTTC | 114792 |
| rs544660544 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119745 | TTAACAGTCTGGCTT[C/T]CTGTATACATTTAGG | 114792 |
| rs544661644 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078515 | AAAATCTGTAATCCT[A/G]TTCAATTTGGACATC | 114792 |
| rs544720062 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979298 | TTAAGTCTTTAATCC[C/T]TCTTGAGTTGATTTT | 114792 |
| rs544731964 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105058 | TGGCAAATCGCAACA[C/T]CTGCTCACTTGCATT | 114792 |
| rs544741727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941113 | TTGTACTTTTGTAAA[C/T]AATTTTTCAAGTCTT | 114792 |
| rs544747691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030156 | AGAGTAACTCCAAAG[C/G]TGCACATAGTTTGCC | 114792 |
| rs544751468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128669 | GCACATTGCTACCTG[C/T]CAACAGGCAGGCTGG | 114792 |
| rs544767025 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994025 | AACAAACCTACCCCT[G/T]GCTCTGGAGGGAGAT | 114792 |
| rs544803120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920324 | ACAACTGTTAGTTTT[C/T]CTTTCCATGGCATTC | 114792 |
| rs544804683 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991305 | TGCTCTGCAATTCCA[G/T]CTGAAGGGTCCTTCC | 114792 |
| rs544812152 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120843 | TTGTTGCTTTAGATC[C/G]TAGCAACCAGCTGCC | 114792 |
| rs544828994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928857 | GAGGCTCTTACAGAT[A/G]CAGATTTTAAGGTTG | 114792 |
| rs544829187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936259 | TACATTTTGCATGGC[C/T]GTTCATTTCTCTAAA | 114792 |
| rs544836568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963733 | TTATACATTCCTTGT[A/C]TTTAAATGTTCAGTA | 114792 |
| rs544838489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056781 | CAGTGGGTCACGACC[A/G]TAGTCTCAGCACTTT | 114792 |
| rs544845084 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071119 | TTCATCTCTCATTAC[C/T]GCAGCTGCTCCTTGC | 114792 |
| rs544855314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023026 | GATATCATGAGAACT[A/C]ACTGACTGTCATGAG | 114792 |
| rs544903945 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903763 | TGGTTAAATTCAACA[A/C]CCATTACTAAAAATA | 114792 |
| rs544906022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099611 | TCTGAGACTATCAGG[C/T]GGCTGGTTCTCCACC | 114792 |
| rs544911629 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064273 | GAAAAACTAAAACTC[A/C]GTTCTTTTGCATTTT | 114792 |
| rs544934275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051102 | GTGCTGAGGAACCCA[C/T]TGTGGGCTAAGGTGC | 114792 |
| rs544959411 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058258 | TAAGCTTTAGAATCT[A/G]TTTGTTAATACACAA | 114792 |
| rs544980180 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901162 | TGCACTCATGACTTT[G/T]GTCATTGTATTCATT | 114792 |
| rs544987943 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992796 | ATTTGCATTTTGCAG[A/G]TGTGGGAACTAAATT | 114792 |
| rs545002024 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038845 | CCCAGCACTCCAGCA[C/T]TTTGGGAGGCTGAGG | 114792 |
| rs545004899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084087 | CCTCAGTAAGGAGTT[A/C]TTGATACTCTCAGGT | 114792 |
| rs545011631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921625 | TGTGACAGAAAACCA[C/T]GACACTGGCATTAAG | 114792 |
| rs545021034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052122 | TGTAAAAGAACAAAC[A/G]AAAGAAGTTTGTGTT | 114792 |
| rs545050792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958648 | GTGGGCCAAGAGCTA[C/T]TGCCTGTATTCATTT | 114792 |
| rs545052721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949007 | CATAAGTAAGATTTT[A/G]GATTAATTTCATTTC | 114792 |
| rs545069673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085044 | GATGAAAACCTTAGT[A/G]AGTCAATCTGAATTT | 114792 |
| rs545071922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989021 | ATGAGAAGTTAATGG[A/G]TGCAGCACACCAGCA | 114792 |
| rs545080674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052631 | GCATCTAGCCTCCCA[A/G]CCACTGCCCAATAAA | 114792 |
| rs545100235 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948407 | TTTAATAATGTGGAG[-/A]AAAAAAATTCAACCA | 114792 |
| rs545128948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093531 | TTATATATCTCATAA[A/G]TCAAACGTTTTTATA | 114792 |
| rs545128964 | snp | A/T | 0.000150194 | 0.00866455 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967119 | CCTCACATGCCGTAG[A/T]GAGCCCTGAAATAAG | 114792 |
| rs545136352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959065 | ACTTCCCAGAGAAAA[A/T]TTCCTCCAAGAGTGG | 114792 |
| rs545179756 | in-del | -/CTG | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909105 | AAGACCAGCTGACTT[-/CTG]CTGCTGGATTTTTTT | 114792 |
| rs545184175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944852 | GTGGAATCTTCTGAA[G/T]CTATTCTTCATCGAA | 114792 |
| rs545184952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121593 | AAAGAATTACATACT[A/G]CAGGAGTCTAATGGC | 114792 |
| rs545189035 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021074 | GAGAAAAAAAGATTT[A/C]TTATAAGGAGTTGGC | 114792 |
| rs545189764 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985631 | TTCATTTCATCTTCC[A/G]TCACTGATACCCTTT | 114792 |
| rs545194704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996323 | CGTTAGAGGCTGGGC[A/G]TGCTCCTGCCTATGT | 114792 |
| rs545201766 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082519 | TCGGGAGGCTGAAGC[A/G]GGAGAATGGCATGAA | 114792 |
| rs545208260 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999776 | AATGTGCTTCTTTAT[A/T]ATGGTTCTTAATGTG | 114792 |
| rs545219807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071797 | CCTCCTTGTCATTGA[C/T]GTCATTCGGGTTGGG | 114792 |
| rs545240641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079961 | CTACCTGGATACTTA[C/T]ATTTTTAAGTCACAG | 114792 |
| rs545264889 | snp | A/T | 0.000149677 | 0.00864963 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085135 | ACCCAGGAATTAAAT[A/T]GCTTTAATTACTTGG | 114792 |
| rs545273144 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986259 | GAGGAGTATCCGGCC[A/G]TGTGAGGTGTCAGTC | 114792 |
| rs545282694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064883 | AAGCTGAGAAGTTCC[A/T]AGGAGGGCGGCTGCA | 114792 |
| rs545297112 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016820 | TGGTTGGATCCTGCG[A/G]TTGGTTTACCCCATG | 114792 |
| rs545341344 | in-del | -/GTTTT | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121630 | AATTGGTGTTGTAAA[-/GTTTT]GTTTTGTTTTGTTTT | 114792 |
| rs545348197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039128 | AGAAAAAGAAAATGG[A/G]ATTAACTAAGTGCTC | 114792 |
| rs545350596 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122703 | TGTAGCAAACTTCCC[G/T]CTGTGGATTGTCTCT | 114792 |
| rs545355753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981820 | TTTACCCGAAAATCA[C/T]TCAGGAGCAAGTTGT | 114792 |
| rs545386641 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982524 | CTCTCTGCCTTTTAA[C/T]TGGGGCATTTAGTTC | 114792 |
| rs545412581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108185 | CACTCTTGCTGGCTT[G/T]GCCACCAAAAATGCT | 114792 |
| rs545416930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009714 | TGCTGGACAGTAGAA[A/G]GAAAGACTGCCTGTA | 114792 |
| rs545422747 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013368 | TTGTGCCTTGGTTTC[A/G]TTGTTGTAAAATGGA | 114792 |
| rs545438858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101403 | TCAAGAATAAGCCTC[A/G]AGTTTTATGATATTA | 114792 |
| rs545454191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003203 | TTCTGACTGGTATAA[A/G]ATGGTACCTCATCAT | 114792 |
| rs545470161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937711 | CTTCCACTTCCTCCC[A/G]TGTCCCCCTCTACCC | 114792 |
| rs545512970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102726 | AAGAATGGGTTTCAT[A/T]TTTCCTATGGCATCA | 114792 |
| rs545538905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116731 | TAGACTCGCTAGATC[C/T]GTCGTCCTGGTATCA | 114792 |
| rs545544826 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996925 | AAGTAAGAGCTGATG[A/G]TGGCCTGAAGTAAGC | 114792 |
| rs545553379 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132390 | GTTCTACATGGCTTA[A/C]TATTGCTGTATTTAA | 114792 |
| rs545584284 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005028 | AGTACATCCTCCCCA[A/G]TGTTTTTGAATAGTT | 114792 |
| rs545585792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018931 | AACTGACAGATCATA[C/T]AGATTTTTTTAAATG | 114792 |
| rs545590439 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069361 | AAAAATGCTATTCTC[C/T]CACTAGGGAGTTAAG | 114792 |
| rs545601234 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931076 | GCTGAATTATGTAAA[G/T]TTTATGAAAAGGTCA | 114792 |
| rs545604361 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917460 | TCTGACCTGAGGTCC[A/C]TGCCCCAATCTGTTA | 114792 |
| rs545604636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908734 | CAGCTGTCCACTGTC[C/T]GCACCCCCCTCCCTT | 114792 |
| rs545606412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976471 | GCTTCATGTGGGGGT[A/G]CAGACTGGAGTGAGA | 114792 |
| rs545609423 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898014 | CTTCGGGGCGAGTGA[C/T]GGCTCCCACGAGGGC | 114792 |
| rs545622133 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922775 | TAGTTGCTCCTCTAG[C/G]AGTGGAGTAAACTGC | 114792 |
| rs545629981 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130317 | AGTAAATTGCTCAAG[A/T]TCACATACAAGTTAT | 114792 |
| rs545648775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943293 | AGAGTTCATATTCCT[C/G]TAGAACCAGCTCTTA | 114792 |
| rs545649505 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938649 | GCAGCAGCAGCAGCA[A/G]CAGGGGATACATAGA | 114792 |
| rs545652555 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925892 | TATACACAGATAGAG[A/G]TAGATATAAAATGTG | 114792 |
| rs545664756 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898507 | TATTTTTTACATCCC[A/G]TTCTCATTTGACCTA | 114792 |
| rs545671701 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012566 | TGTTGTTTTAAACCA[A/C/T]GAAGTTTGTGGTACT | 114792 |
| rs545676231 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140054 | GTATTTTATTGTCTT[C/T]AGAACCTTGTAATTG | 114792 |
| rs545689221 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130904 | ATAGATTCTTACAAC[A/G]TAGACACTGACCAGT | 114792 |
| rs545692272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968293 | GTGGATACATTTGGC[A/G]TCTACTGGGTAGAGG | 114792 |
| rs545707027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998862 | ATGCATTACATGGTA[A/G]ACTGATCGTTATTTT | 114792 |
| rs545708202 | snp | C/G | 0.0185938 | 0.0946107 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142625 | TTTGGTGAGGTTTCT[C/G]TATCTATTTACCTTT | 114792 |
| rs545711721 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897085 | GCGCGCCACCACGCC[C/T]GGCTAATTTTTGCAT | 114792 |
| rs545717761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937115 | TCACCCATTGTAACT[A/G]TGTACAGTTCAGTAG | 114792 |
| rs545720233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123460 | CTTTTCATTCCTTCT[G/T]GCAGTTTTTAAAGAC | 114792 |
| rs545721509 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050062 | TGCTCAGAGTCTAGT[C/T]TGTGCTGCAAGAATC | 114792 |
| rs545737488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132488 | TCTGAGAAATAGTGC[C/T]TAATTTTTCTGAGTA | 114792 |
| rs545739907 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140791 | GTTATACACAAAACA[C/T]TGAAAATACATAAAA | 114792 |
| rs545751470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909627 | CCTAAGATGCTACAG[A/G]TGGTTAGAGGCAGGT | 114792 |
| rs545753835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999414 | AACAACAACAACAAA[C/G]AGTTAATTTCCGTTT | 114792 |
| rs545776548 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900989 | TTGGGTCTGTAAAAC[C/G]TAGAATACTGGGAGC | 114792 |
| rs545796840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901674 | TGCACAGATCATCCC[A/T]TCACCCAGGTATTAA | 114792 |
| rs545804952 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132889 | ACTAGTTCAGCCACT[A/C]AACTTCATCCTGTAT | 114792 |
| rs545816483 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066248 | GATGCATGCTGACAC[A/G]GTTTGGTTAGAGCGT | 114792 |
| rs545824212 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905398 | TGTGTTTGTTCTCTC[C/T]GTCTGTCTGGTCCTT | 114792 |
| rs545849295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018408 | CCTGGCCAACATGGT[A/G]AAACCCTGTCTCTAC | 114792 |
| rs545857156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095767 | TGATCTGCTGAGGAA[C/T]GCAGCCCTTGAGAAA | 114792 |
| rs545871546 | snp | C/T | 0.00015957 | 0.00893083 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976000 | TCTCCTTTGTAGTAT[C/T]CAAGAAATGCTGACA | 114792 |
| rs545913482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060106 | CTCAAATCCTTCAGT[A/C]CACTGTACACATAGA | 114792 |
| rs545930146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126252 | GTAAGGCAATATTTC[C/T]AAAGATAGATTTCTT | 114792 |
| rs545937469 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968585 | CTTTTAAGTCTGCCA[C/T]CCCGTTCTTATTAAT | 114792 |
| rs545941666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945552 | GCCTACTCAGACTCA[A/G]GACCAAGTCCTAGAA | 114792 |
| rs545958268 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924367 | AGACTGCGCATGTGA[C/T]CCAGGGGCCGGCGAC | 114792 |
| rs545965829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028109 | GCAAGGCGGGGAGGA[C/G]TGACTACCCCAGCTG | 114792 |
| rs545975435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916258 | GGCTGCTAGGATTGG[C/T]CAAAACTCAGATATT | 114792 |
| rs545984476 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939163 | TCATTGCAGGATGAA[A/T]GTTAGAAAATACTGA | 114792 |
| rs546038219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960060 | AGTAAATTCCTTGAC[C/G]TCATTATGCCTTATT | 114792 |
| rs546044443 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054446 | TTGGTGCTTTCTCAC[A/C]GTAGGTCAAACTGTG | 114792 |
| rs546045427 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002202 | TGCTCAAAGACAGCC[C/T]GGCAGAGAGAAGGAA | 114792 |
| rs546056807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914899 | CAGACACCCAATCAG[C/T]GTAGCACACTACAGC | 114792 |
| rs546065044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047297 | TCTTCTGGGCACACT[A/G]TGTTTGGGACACTGC | 114792 |
| rs546076286 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960571 | ATATGTGATAATAGC[A/C]TGAATAAACCAGTGT | 114792 |
| rs546085002 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032197 | AGGGAGTTGTTTGAA[A/G]TACATAAGTAATACA | 114792 |
| rs546085510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088777 | ATGGCAATTCTTCAT[A/T]AAAAAAACTTAGAAC | 114792 |
| rs546108811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003446 | CCATTCTCTATAGTG[C/T]CTGTTTACTCTGTTG | 114792 |
| rs546123259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926618 | TTTCAGATGTGTGCA[A/G]GGATCTGACAAGTGA | 114792 |
| rs546126523 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040424 | GCCATTTGGAGAATT[C/G]GTTGGGGGCAAATTC | 114792 |
| rs546130587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991948 | GTCCCTAATCACTGT[G/T]CTCCCTCCCCAGCCT | 114792 |
| rs546139792 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119362 | TTTGGTTTCTCAGAG[C/T]AAATCTAAGTGAGAT | 114792 |
| rs546150000 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048268 | TATCCGGGCTTCTGA[A/C]GAAGGATGCCTTGGG | 114792 |
| rs546153267 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932014 | AGGAGATTTATTTTG[A/G]TAGAGTCTCTCGTTC | 114792 |
| rs546161820 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952814 | CCTAAGGTTGGTCTT[A/T]TGAGATGTTTTTCAG | 114792 |
| rs546179023 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061785 | CAGGTGACAGATAAA[A/T]TCACCACACTGTAAA | 114792 |
| rs546186602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081492 | TCAGTGAAACCCCAG[A/G]TGCCAGAACATGGAG | 114792 |
| rs546207772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969894 | GGATGTCTTAAAGAC[A/G]ACTCAAACTTAACAT | 114792 |
| rs546216122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986961 | CCTGTCTTCTGCATC[A/G]CTCACGCTGGGAGCT | 114792 |
| rs546223360 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060934 | GAATGGGAATCAGTC[A/G]TGGCCCTCTCCTTAT | 114792 |
| rs546228462 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993205 | ATAACAAAGTACCCG[A/G]AAACCTAGAGGCTGA | 114792 |
| rs546230919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082371 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 114792 |
| rs546264267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082145 | TGCAAGAAGTCCAGA[C/T]GGGATGATAAGGAAC | 114792 |
| rs546269326 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030043 | AATGCTTATAAAATG[G/T]AAGGGTTGAATGTAC | 114792 |
| rs546284740 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062959 | AGTGGCCCAGGCAGA[A/G]CAAACAACTAGTTGT | 114792 |
| rs546294289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075739 | AGGTAGTCACATAAT[A/T]CCTTGATTTATAACT | 114792 |
| rs546303358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041250 | AAATGAGACTGTGTA[C/T]TACATATAGAAGTAC | 114792 |
| rs546305456 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992870 | GTAGAAGAGCTGATT[G/T]TCACACATCTGTCTC | 114792 |
| rs546349305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983794 | TATTAGTCTTGCTAG[C/T]GGTCTATCAATTTTG | 114792 |
| rs546359030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019615 | AATGAAGAATTCTTC[A/G]TTAAAGAGGGATCTG | 114792 |
| rs546390849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075928 | AATATTTTTTGATCT[C/T]CATAGTGTGCTCCCA | 114792 |
| rs546412357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061316 | TAGTTTGGCTTCTTT[C/T]AGGGTTTCCTTTCCC | 114792 |
| rs546419974 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939438 | ACAATTAAGAGTGAG[A/T]TTACAATACAAATAA | 114792 |
| rs546421289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977240 | AAATGACCATTTTGC[A/G]TATATGGAAACAATA | 114792 |
| rs546437330 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984185 | TTCCATGTAGTTGAG[C/T]AGTTTCGAGTCAGTT | 114792 |
| rs546444957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013568 | CACACACATACACAC[A/G]TGTACACGTGTCAGG | 114792 |
| rs546456816 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070066 | TCATTTTTCTTCAAC[A/G]CTGAACCATTTTTTC | 114792 |
| rs546507819 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069101 | CCTCAGATTGAAGGC[A/T]TTGTTCTGTTTACAG | 114792 |
| rs546527186 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104985 | TTCTGGTTTATGACA[C/G]CATTATTTCACCTTA | 114792 |
| rs546540211 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104698 | CCCTTGAAAGATCTG[G/T]CTTACAAGGAAAATG | 114792 |
| rs546550764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111454 | AGCAGAGGTAAACTT[C/T]ACTCACTCGAACCCG | 114792 |
| rs546565505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992291 | AGGGACTCTCACTGA[C/G]TCACTCACCGTTTCC | 114792 |
| rs546570225 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094581 | CTTTCCTCTGACCAC[C/T]TCCTCCTTGTTACGT | 114792 |
| rs546575659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911060 | ACACCTAATGCTTTG[A/G]TATTCTGAATTAGTT | 114792 |
| rs546618020 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014312 | AAAAAAAAAAAAAAG[G/T]TTCTTTTTTCGTATC | 114792 |
| rs546639964 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133342 | AGACACATTCATAGT[A/T]TTATTCCTATTATTA | 114792 |
| rs546645890 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916615 | TCATTGGTTCTTCCA[C/T]TCTTTTCTATGAAGG | 114792 |
| rs546658824 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007425 | CTTGGATTGGGTTTT[G/T]ATTTTCTCTTGAATA | 114792 |
| rs546697741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911966 | ATCTCTTCCTGTTGC[C/T]GGCTTCAATTTCCAT | 114792 |
| rs546722907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118356 | GGGTGCAGTGGCTCA[C/T]GCCAGTAATCCCAGC | 114792 |
| rs546726844 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987901 | AACTGGCTAGCCATA[C/T]GTAGAAAGCTGAAAC | 114792 |
| rs546744526 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906911 | ATATGTCCAGAGAAG[G/T]CTTCCAGAGAAGTCT | 114792 |
| rs546745277 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135268 | CCTTTGGCTGGCACA[C/G]TGGTCCTACAAAGCA | 114792 |
| rs546764169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126682 | TCTGTACTGAGATGC[A/G]TTGTGTCAAATATAC | 114792 |
| rs546778375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018237 | ACAACAGAAGATGAC[A/C]GATATTAGACCAAAT | 114792 |
| rs546796903 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106062 | GATATATACAAGCAG[C/T]TGGAATTCAAAACAT | 114792 |
| rs546800815 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NDUFAF4 | GRCh38.p7 | 6:96896077 | ATATACTCAGCAGTG[C/T]ACGTACTTTTCCCAT | 114792 |
| rs546806896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135949 | GGAATAATATTTATG[A/G]GAAAATGCTTAACAG | 114792 |
| rs546819217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995177 | AAGCATAGTACCTGA[C/T]ACTCAATAAATGTGA | 114792 |
| rs546820413 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063606 | CGTGCTGAAGTAGTA[C/G]AGTGGAGGGGTGAAT | 114792 |
| rs546851595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029142 | TGTCCTTTTTTTATT[C/T]CACCCTTTCCTCTCC | 114792 |
| rs546855410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083352 | CTGAGATCGCACCAC[C/T]GCATTCCAGCCTGGG | 114792 |
| rs546864032 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896665 | AGAGCACTCTTTTTA[C/T]TACTTGCCACACTTA | 114792 |
| rs546868180 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128196 | TTGGCTTTGGCAGTC[G/T]GGGTTGGGACTGGCC | 114792 |
| rs546868687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020582 | CCTGTTCTAAAGTCC[A/G]GAAGAAGATGGAAAG | 114792 |
| rs546902424 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035627 | CTTGGCAGTTTTTTT[C/T]TTTCAGTATTTTGAA | 114792 |
| rs546926151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062546 | CTTTTTCACTTCTTT[A/G]CTTTGCCACTTAGAA | 114792 |
| rs546935107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940687 | TAATAAGCTGAGTTA[C/T]AGAAAACAGGCAAAT | 114792 |
| rs546937701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029812 | GTAATAAAGGCTAAT[A/G]ACCATTAACACTAAA | 114792 |
| rs546966679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056207 | GCTTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 114792 |
| rs546972738 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919095 | TTGACCAATTAGATT[A/C]TCCTGGGAATTTGAA | 114792 |
| rs546973310 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056254 | GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC | 114792 |
| rs546974459 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022404 | TTGCCCTCTGCAGGT[A/C]TTTGCTCAAATACTG | 114792 |
| rs546981751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971259 | TAAAACCATATAGCT[C/G]TTTTCGGAATTTACA | 114792 |
| rs547000275 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984889 | TTAAGGTTAATATTG[C/T]TATGTGTGAATTTGA | 114792 |
| rs547010929 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035586 | TTCATTTATTTTTAA[A/G]GGATAGTTTTGCCAG | 114792 |
| rs547018744 | in-del | -/TTCA | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101608 | GTCTGTCTCTCCCTT[-/TTCA]TTCATTCATTCATTC | 114792 |
| rs547018843 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120535 | GAAGAAGGCAGATCT[C/G]TGGATTCACTCATGA | 114792 |
| rs547038560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919914 | AGGCATTTTATAAAA[C/T]TTGCCTCAGTGGAGG | 114792 |
| rs547039550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007853 | GGTTAGGAACCTGCT[G/T]CACTGGAGGGGCCAA | 114792 |
| rs547042212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023096 | CCCACCAGGTCTCTC[C/T]CTTGACATGTGGGGA | 114792 |
| rs547064563 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928500 | ACTAGGAGAGGAGTT[G/T]TAGCCATAGAGGAGA | 114792 |
| rs547102649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063809 | CACTGGGCTGGGGAA[A/G]TGGGTTAGAATGGAG | 114792 |
| rs547120264 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006762 | TGAAACTTAGTTTGG[A/T]TAGGTATGACATTCT | 114792 |
| rs547129433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016094 | TGGAGCCCTCATGGA[G/T]AACCTCTGCTAGGGC | 114792 |
| rs547143337 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028477 | CCCCCTCTCTGTCTC[C/G]TCAGTTGCTTCACTT | 114792 |
| rs547147144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921723 | CATAGCTCTCTTTCA[C/T]GATGTAGTTTTAGCT | 114792 |
| rs547148711 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956075 | AGGCACGTCTCATAT[A/G]GTGGCAGACAAGCAA | 114792 |
| rs547149970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091969 | CCTGCCCTTCTTCAA[A/T]TCTCTTTCTTTCTTT | 114792 |
| rs547166480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903948 | AGCACTTCTGTCTGC[C/T]TTGAAAATTATAGAG | 114792 |
| rs547172585 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043382 | GTTCATCCATGTCAT[G/T]GCAAATGACAGGATT | 114792 |
| rs547185726 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986229 | CCGGATCGTTCCTCT[A/G]GAATTTTTGTCTCAG | 114792 |
| rs547204365 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051500 | TCAGTGGGTTTTGCA[C/T]TTCTGTGCACCTGTT | 114792 |
| rs547236559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947974 | CTGGTCTTGGCATAA[A/G]GAAATGAATTGTATG | 114792 |
| rs547250165 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955437 | TCTCTTTGATCTTGG[C/G]GGTTTATTGTTGTTT | 114792 |
| rs547257283 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135982 | GAAATTCCTAAGTAT[G/T]TCAGTGGGTTGAGAA | 114792 |
| rs547273229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948600 | CTAATAGTATTTAGC[A/G]GTTTTAAGTACAGGA | 114792 |
| rs547288151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989050 | CATGGCACATGTATA[C/T]ATATGTAACAAACCT | 114792 |
| rs547315697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941435 | CTGAAAAACCTGTTG[C/T]TATTCCCATTAAGAA | 114792 |
| rs547319209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077967 | ATAGCTTAGTGACAA[A/G]CTTATGTGTATGTGA | 114792 |
| rs547319699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949548 | TCATTTTTATTTTTG[C/T]AAAAATTGTGAATAT | 114792 |
| rs547334183 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103502 | ACAGGCGCCCAGCCA[C/T]GTATAAAATCTTATT | 114792 |
| rs547350966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934908 | GTATGGATATAGCAC[A/G]ATATGAGGAGCAGAG | 114792 |
| rs547380553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070713 | AGCTAACTGTTGTCA[A/G]CTGGGTGATTTTAAA | 114792 |
| rs547388615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085423 | TGAGGAACAATTACC[A/G]CTATTTTAGTGGCTT | 114792 |
| rs547407289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958741 | CTAGGCAATGTTTCC[C/T]CACCCATTGGAAAGA | 114792 |
| rs547428047 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079486 | TTGCCTTTCCCATAT[A/T]TTTACCCCTACCGTA | 114792 |
| rs547436898 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050588 | GAAAGCCATCCGGAG[A/T]GAAATAACAAAAATA | 114792 |
| rs547441086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113482 | ACAGGCTGTTTCACA[A/G]CAGCATTTTCATTCT | 114792 |
| rs547442653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942794 | CCAGGTTATTCTGAT[A/G]CCACCACCTCCCTTT | 114792 |
| rs547447426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071326 | ACAGCATTTAAACAC[C/T]GGGAGCTGCATTCTT | 114792 |
| rs547467903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989589 | GTCTTGGGGATGGTC[A/G]TCTTGTATAGTATCT | 114792 |
| rs547500412 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980472 | TCACATTTATTTATT[A/T]GCATATAGTGAACCA | 114792 |
| rs547520299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057827 | TGTCATACCCAAAGT[A/T]ATCTAGATCTTCTCC | 114792 |
| rs547543790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981229 | CTTCTTACTGATTCA[A/G]TTTTGGAACTTCTTA | 114792 |
| rs547577010 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080046 | ATATTAAAATCTTTT[C/G]ATCTAAGTAGCCAAT | 114792 |
| rs547582239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965828 | GTCCAGACTTAAGTT[A/G]GAAATAAATGGAAGT | 114792 |
| rs547597646 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983865 | TTTGAAGGGTTCTTT[C/G]TGTCTCTATTTCCTT | 114792 |
| rs547610076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065845 | AATCTTCCCAGCAAC[C/T]CTGGAAAATAGGAAC | 114792 |
| rs547614803 | snp | C/T | 1.6939e-05 | 0.00291019 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114555 | AACACACTTTCATTG[C/T]GGTATATATTTAAAA | 114792 |
| rs547620497 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037159 | ATTTTTTCAAATTGT[A/G]TTTAAAATATATTTT | 114792 |
| rs547625412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031874 | TGCTGTTTCTCAGCT[A/C]TCGTTTCAATTGGAG | 114792 |
| rs547627620 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130071 | CACTGATCTCAGGAG[A/G]TTAATTTTGGAAAGA | 114792 |
| rs547664426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958122 | CAAATGGGATGTGAT[C/T]AGTAAATTGCACTGG | 114792 |
| rs547709897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102085 | TACTTGTTTTGCTGA[A/G]TATCAGTATGTTGAT | 114792 |
| rs547722542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137959 | ACACCTACGTCCAGG[A/T]TGCAGATGAAGGAAA | 114792 |
| rs547733799 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971749 | GGAAAAAAACAGAGG[G/T]ACATATATCCCTGGG | 114792 |
| rs547737769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093661 | GTCTCCAATAAAGTC[A/G]TACAGGAAAGTGTTG | 114792 |
| rs547753581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930835 | GGTCACAAGGAAAAG[A/G]AGGGAGGGTCAGTCA | 114792 |
| rs547770665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094778 | ATTGGTAAGTGGCAC[A/G]GTATTACTTATGCTT | 114792 |
| rs547772363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102791 | AGGACATTTTCGCCA[C/T]TTAAAAGTTTTGTAT | 114792 |
| rs547790179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967827 | CCTTCCTGAGAAAGG[C/T]TGTATACCTGAGATT | 114792 |
| rs547793465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037577 | TTCATGGATAGGAAT[A/G]ATTAATGCTGCTAAA | 114792 |
| rs547801295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109525 | AGATCACAGTGGTCA[C/T]CGTTCCATGGCTAAT | 114792 |
| rs547802389 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025391 | TAATGAGAGATTTTC[A/C]TATCAAATCATTCAT | 114792 |
| rs547809747 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002585 | ACTCAGGTCCTAAGC[A/G]TAGTACGCTATAGGT | 114792 |
| rs547809982 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897513 | TCAATGTCACCGGCC[G/T]GGCGGCTCCCCCTTC | 114792 |
| rs547820881 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087582 | AAAAGGTGTTGGGGA[A/G]GAGAAAGGAAATTGG | 114792 |
| rs547822298 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898040 | AGGGCCGCTTCCGGC[A/G]GGAGGTGGCGGGGCT | 114792 |
| rs547828350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129654 | TGGGAGGCCGAGGTG[G/T]GTGGATCACCTGAGG | 114792 |
| rs547831807 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031247 | TCTTTTAAATGTATT[A/G]TACCCAAGACATTGA | 114792 |
| rs547842799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095406 | GCTCTTCTCATCTCA[C/T]GTAAGTTTTAGGCAA | 114792 |
| rs547854771 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047048 | ATAGAGTGGGAGTGA[C/T]GAATGAATGCCTCTA | 114792 |
| rs547873769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011947 | TAATCCCCCCAATAA[C/T]CCTTAAATGTAGATA | 114792 |
| rs547890545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986057 | GGGGTTTTGGTGTGG[A/T]TGTCTTTTCTGTTTG | 114792 |
| rs547894474 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957183 | CACATATTTGATGAA[G/T]GAACAGTCTATATAT | 114792 |
| rs547902287 | in-del | -/TTG | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912987 | GAAGCTCGCAATTTT[-/TTG]TTGTCTGAATGAATA | 114792 |
| rs547910546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005091 | ACCTGGTAGAATTTG[A/G]CTGTGAATCTGTCTG | 114792 |
| rs547915171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936684 | TAGACTCTTCTCCAC[A/C]CAGCAGCCAAAAATT | 114792 |
| rs547916373 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048433 | GATCTTTACAAGGAA[A/G]TATTGTATCACCATT | 114792 |
| rs547953708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122938 | CAGAGAACTTGAGAT[A/G]GTTTTCCTCAATCCT | 114792 |
| rs547958084 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024516 | CCAGGTAACAGTGAT[A/G]TTGGTCAAATGTTAC | 114792 |
| rs547972129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115242 | GCTGCCCTTGAACTC[C/T]TGAGCTCAAGCAATC | 114792 |
| rs547974833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991334 | CCTGGGGAAGAATAC[A/G]GGGTGGGAGCTCACA | 114792 |
| rs547982715 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133076 | TTCCTTCATATCCCC[C/T]AAGCTTTACAAATAC | 114792 |
| rs547991798 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125348 | ATTCTTGTTGACTTG[A/C]CTCCTAGCCATGTAG | 114792 |
| rs547995889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017237 | ATGCCATGTCCTTGA[A/G]ATTTAGGAGATTAAT | 114792 |
| rs548011663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992202 | GAGATGCAGCTGCCG[A/G]TGTCCGGTACCAGGG | 114792 |
| rs548014508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908953 | TGAAACCAGGAGAAA[C/G]TGAATGAACACTGCA | 114792 |
| rs548033355 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140327 | GTACCATAAAGTGCT[C/T]TGACATAAATTTGAA | 114792 |
| rs548077801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011253 | GGAGACATGTTCTTC[C/T]TTGAATCCTGCAAGA | 114792 |
| rs548086613 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099705 | CCACTTCTCCCACCC[A/G]AACTAAGCCCTGCCC | 114792 |
| rs548109377 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047360 | ATGGGTGTCCTTGCA[C/G]AGCCATGCATGGAGG | 114792 |
| rs548125978 | in-del | -/TG | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971607 | AAAAGGTCATCTTAC[-/TG]TGTTCAGGGAGTCTG | 114792 |
| rs548137741 | in-del | -/AAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909888 | ATTGTAAAAAATCTT[-/AAG]AAGACAGATGGTAGT | 114792 |
| rs548137882 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967440 | GTATATATATATATA[G/T]ATGTGTATATATAGA | 114792 |
| rs548151301 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923656 | ATTAAGGACACCTCA[A/G]AATAGATCAGGGCAC | 114792 |
| rs548152099 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110336 | TCCTTGGCACCTAGC[A/G]ACATTTCCTTTTTCA | 114792 |
| rs548163140 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924413 | CGAGGAGGAGGGCGG[C/T]GTGGAGGAGGGTACT | 114792 |
| rs548167062 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909269 | TAGACAGAAAAAAGA[C/T]AGAAGATAGAAGAGA | 114792 |
| rs548178454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118018 | CTGAGTCACAGATAC[A/C]TGAAATTAATTTAGC | 114792 |
| rs548178761 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951454 | TATTTTAAATAGTTT[C/G]CAAAGAGGGCTGGGC | 114792 |
| rs548201770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985874 | TTCTTGTCTCAACTC[A/G]TCAAAGTCATTCTCC | 114792 |
| rs548234679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026830 | TGAGGAAATTCCACA[C/T]TATTATCTTCAACAT | 114792 |
| rs548256285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932773 | TGGGTGTCTCACTAT[A/G]TTTCCCTGGCTGGTC | 114792 |
| rs548266315 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049876 | ATAAAATATGAACAG[C/T]TTTGTTGGTCCCAAG | 114792 |
| rs548287569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013825 | ACTTTGCAACTTGCT[C/G]TGACTTATTATATTG | 114792 |
| rs548291155 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979026 | TAATTTGTTTAACTT[C/T]TTTATAGATTCTGGA | 114792 |
| rs548294072 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899368 | TAATCTGCCTCATTA[A/T]GTCTATGTGCTTTAA | 114792 |
| rs548304162 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951477 | GGCTGGGCCATGTGG[G/T]GCATGTTGGACAGTG | 114792 |
| rs548319619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917142 | TTATGTTGGAAATTA[C/T]AAAACCCAAATTAAC | 114792 |
| rs548320816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131723 | ATGCTGAGTGGGCAC[C/T]CAATCCCTTGCAGCT | 114792 |
| rs548327718 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918063 | ATGTCCCCTGAGGGA[A/C]AAAATCACCTTTTCT | 114792 |
| rs548337972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951976 | CTGTGTGAAGTTTGC[A/T]CATTCTCCCCATGTC | 114792 |
| rs548359036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110844 | CAGAAGCCTGCTGCT[A/G]TTGGTGTGGGGATGG | 114792 |
| rs548375412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901161 | CTGCACTCATGACTT[C/T]TGTCATTGTATTCAT | 114792 |
| rs548387668 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032868 | TTAATTTTGGAATTT[C/T]GGGTAATCTTCTGCA | 114792 |
| rs548395857 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970682 | AATGAGGGAAGGAAG[G/T]AAACAAAACTATTCA | 114792 |
| rs548396090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986744 | TATTAGGGTGGGAGT[A/G]ACCCGATTTTCCAGG | 114792 |
| rs548425930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944162 | TGATTATTAAGACGG[C/T]AATTACTGATCATGC | 114792 |
| rs548444534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074249 | TCCTGTTTCAGGAGG[C/T]CTGGGGAGGGCCTAA | 114792 |
| rs548450107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055701 | TAGTTGAGAGGTTGA[C/T]GTGAAAGAATTGCTT | 114792 |
| rs548463023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945084 | TAGGTCTCTTGTTAT[A/G]AACTACTTAAAATAT | 114792 |
| rs548470639 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981227 | TTCTTCTTACTGATT[C/G]AATTTTGGAACTTCT | 114792 |
| rs548504910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961820 | TAATGGAGTTTTTGG[A/C]TCTCTGATATCAAAA | 114792 |
| rs548506396 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075008 | TTAGTTATTGTTGAC[A/G]GCTATGTTTCACTTC | 114792 |
| rs548533580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96999986 | GGGAGGGAAAGAGAG[C/T]AGGAAAAGAATGTCT | 114792 |
| rs548590377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939517 | AGCTTTGACCTGCTC[C/T]GGAGGTTGATGAGGA | 114792 |
| rs548592367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947207 | AATCATATCCAAATA[A/G]GGCAAACACCTAACT | 114792 |
| rs548615253 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000745 | CAAAAACATTCTCTA[A/T]AAAATACTGCACATA | 114792 |
| rs548628605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939829 | AGATCTGATTACAGG[A/G]GAACAGTAATCAGAA | 114792 |
| rs548628762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902007 | TTAGGTTGATTCCAT[A/G]TCTTTGCTATTGTGA | 114792 |
| rs548629395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103420 | GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG | 114792 |
| rs548629891 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068242 | ATTGTTTTATTAACA[A/G]CCATTCTTTATGTGC | 114792 |
| rs548649129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961897 | CTTGTGAAGTTGAAG[A/G]TCTCAACTGGCTTGA | 114792 |
| rs548651065 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930368 | ATACTAAATCTGATA[A/C]TTCTTGGTTCTGTGA | 114792 |
| rs548651605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134294 | CACATGAAGAGCCAC[A/G]TAAGACTTTAAGGGA | 114792 |
| rs548654203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054881 | GAGGCAGAGGATGCA[C/T]TGGGCTGATATCGTG | 114792 |
| rs548659231 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031990 | TGCCTAACATTAAGC[A/G]TAATTGTATTTAAAC | 114792 |
| rs548677674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069141 | GTGGATCATCGAGTA[A/C]AGCAAAGCCCAAATT | 114792 |
| rs548685379 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968523 | CTCAGCCAAGTTATT[A/T]ATTTCTGGCTACCAG | 114792 |
| rs548688618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082550 | CCCGGGAGGCGGAGC[C/T]TGCACTGAGCCAAGA | 114792 |
| rs548716335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940487 | TGATATCCAAAATGT[A/G]GAGGAGTGAAAGTGG | 114792 |
| rs548724099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034975 | CCTCTCCCATTTGGA[A/T]GCTTTTTATTTCTTT | 114792 |
| rs548732763 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069672 | CGTGGGAGTTCATTA[G/T]GTACTGAGGGATTGA | 114792 |
| rs548735956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961057 | GGGGATTCTCTTCAG[A/T]ATGTAGATTTTCCCC | 114792 |
| rs548738437 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062071 | GTGGAAGGAAAAAAC[A/T]ACAAAACAAAAAATA | 114792 |
| rs548751142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076599 | TTTACCACCCAGTGA[A/G]GGAGACAGGGAAACT | 114792 |
| rs548761525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028332 | CCAAAATTCTATTTG[C/T]AGAAGAGAGGCTAGA | 114792 |
| rs548769859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969143 | TCAGCCTGGAGGATA[C/T]GTCTGCTTCATGGTC | 114792 |
| rs548771000 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998895 | ATCAAATGAATACTT[C/T]GGCTTACACTTAATT | 114792 |
| rs548785773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984261 | AGTTTGTTATAATTT[C/T]TGTTCTTTTACATTT | 114792 |
| rs548791507 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141581 | AATTTCACTGAAACT[A/G]TTCAAATATACATTT | 114792 |
| rs548797490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007213 | CATTTTTATTTATTT[C/T]TGTCTGACTGAAATA | 114792 |
| rs548804805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945905 | ATTATGGTTTTGAGA[C/G]TTAGTGAGACAAACC | 114792 |
| rs548808541 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015103 | CCTTGCTTGCCCCTT[A/G]CCTTCTGCCATGATT | 114792 |
| rs548849546 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971347 | GATTTCTGTGACCAA[A/C]AATGTGAACTCTGTG | 114792 |
| rs548868237 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948185 | GTTACTAATGCTAGA[C/T]GCAGCACAATGTACA | 114792 |
| rs548869822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927152 | TAAAATAGGAATTTT[C/T]GAATCTGGTGAAACA | 114792 |
| rs548883625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000612 | ATGATTATAATTTCT[A/G]TTGAAAATACTTGTG | 114792 |
| rs548893299 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098640 | TTAAGTCATTGAATC[C/T]AGTTGCTGTTTTAAT | 114792 |
| rs548897696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034233 | TTCTATTCTTTGGCA[G/T]GCGGATGTCAAGTTT | 114792 |
| rs548906394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111938 | CACTTCTCTCCAACT[A/G]TAGTCTCTGACATTT | 114792 |
| rs548921799 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134621 | GTAAGTTTGGGTTTA[C/T]CATGAAATAAAATTG | 114792 |
| rs548934660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991911 | GGGTAAGGTGGCTGC[A/G]CTGTGCTGGGGGTCT | 114792 |
| rs548938020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971919 | GTGCAGTGGCGTGAT[A/C]TCGGCTCACTGCAAC | 114792 |
| rs548938104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964113 | TGGCCTTTTTTCATA[C/T]TGCTCTGCTTCCTAA | 114792 |
| rs548955057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902741 | ACATTTCAGTCTGTA[A/G]TCCATCTTGAGTTGA | 114792 |
| rs548971635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105746 | CCTTTCAGTGAAAGA[C/T]AATATTTGTAGACCA | 114792 |
| rs548981214 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138079 | ATAGTTAGAGAAAAG[G/T]CAAATGAAAAGGGAT | 114792 |
| rs548983106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100712 | CTTGAGCCCTTGAGG[C/T]CCATTTGGTTATAAT | 114792 |
| rs548987761 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948863 | AAAACATACTCCACT[-/CTC]CTCCTCTTTTTCTGA | 114792 |
| rs548988521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011094 | GGTAGTGGGAGGAGG[A/G]ACAGCGTTTGGACAT | 114792 |
| rs549012997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126750 | GAAATATATAAAATA[C/T]CTTAATAATTTTTAT | 114792 |
| rs549014599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007956 | AGTGGAATTTGTGCT[C/T]GCTTGCACATGCCAG | 114792 |
| rs549026153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092069 | ATCTCAGCTCACCGC[A/C]ACCTCCGCCTCCCGA | 114792 |
| rs549043835 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988000 | AAAACCATAAAAACC[C/G]TAGAAGAAAACTTAG | 114792 |
| rs549045667 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055211 | CCTCACTAACCTACC[C/T]CCAGTACACATATCA | 114792 |
| rs549046217 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103245 | TTGAGACGGCGTCTC[A/G]CTCTGTCACCCAGGC | 114792 |
| rs549063074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050116 | TCATGTCTAAAATGT[C/T]TCTGTGCAAAGAAGT | 114792 |
| rs549080558 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118800 | TCCAAGTCCTGTTCC[G/T]GGATAGTGCTGGAGC | 114792 |
| rs549080824 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988679 | TTGCAGCACTATTCA[C/T]AATAGCAAAGACTTG | 114792 |
| rs549087225 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995231 | TTGAAATTCCTGGTC[A/G]TGTTCTGCCTAGGTG | 114792 |
| rs549088789 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142503 | GCCTGACAGGCAATA[-/T]TTTTAACTCTAAGAG | 114792 |
| rs549089326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092672 | GGATTGGTGCTCCTA[A/G]TTGCCAGAGCATATA | 114792 |
| rs549109045 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028971 | ATAGGGATCTGAGAG[G/T]GCAACCCAAGGCTGA | 114792 |
| rs549118642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956261 | TTGGGTGGGGAAACA[A/G]CCAAACCATATCAGA | 114792 |
| rs549118901 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984628 | CCCTTTACCATTAAG[C/T]AATGGCCTTGTCTCT | 114792 |
| rs549126928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904171 | ACATACTAAAACCCC[A/G]TCTCTACTATAAATA | 114792 |
| rs549137436 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969906 | GACAACTCAAACTTA[A/G/T]CATGTCCCAAACCAA | 114792 |
| rs549137745 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119372 | CAGAGCAAATCTAAG[G/T]GAGATAATAGGAGGA | 114792 |
| rs549145616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934438 | CTCAGCTTTCTTGTC[A/G]TTGACACTTAACAAC | 114792 |
| rs549204958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978787 | GCATTCTCTTTTCTC[C/T]GCAACCTCTCCATCA | 114792 |
| rs549210020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989491 | GATGGGTTTCTGTTT[G/T]TATATGTGATTTGCC | 114792 |
| rs549232839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084494 | CTGAGGCTGAGAAAA[A/T]AACAAAGAACAATTA | 114792 |
| rs549239390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927843 | CTGCCCTCAATGATT[C/G]AGAGCAAACACACTG | 114792 |
| rs549271136 | in-del | -/TTGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983326 | TGTTCATCAAGGATA[-/TTGG]TCTAAAATTCTCTTT | 114792 |
| rs549278290 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899116 | CACTGCAAGGAAGAC[A/G]GCTTCAGCCACTCTA | 114792 |
| rs549278973 | in-del | -/ACA | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114757 | AATTGTTGGTCCATC[-/ACA]ACTGTTTTTTTCCTA | 114792 |
| rs549304175 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121688 | ACAAAACTCTTCTCA[C/T]GGAGAGAACCCCCTT | 114792 |
| rs549305282 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101674 | TTTAACAAAGCCACA[G/T]AACTTAAATTACTGG | 114792 |
| rs549309781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015878 | GACTTGGTCCCCTGC[A/G]TCTCAGCCATGGCTA | 114792 |
| rs549312938 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897437 | GGGAGCACTGGCTGC[C/T]GCCTCTGGGTCTCGG | 114792 |
| rs549314379 | in-del | -/AA | 0.0182005 | 0.0936428 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038326 | AAACAGTTCACTAGC[-/AA]AAAAAAAAAATCCAA | 114792 |
| rs549314721 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051090 | GGCACCAATTCTGTG[C/G]TGAGGAACCCACTGT | 114792 |
| rs549335542 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988646 | GCTGCTATAAAGATA[C/T]ATGCACACGTATGTT | 114792 |
| rs549348785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016506 | GAACGAGTGTATTTA[C/G]CCAATGCTTGTACAC | 114792 |
| rs549352359 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920589 | ACACACACACACACA[C/G]ATCTCCCTCCTTCTC | 114792 |
| rs549352707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912627 | ATAATATTTGCTCCA[G/T]GAATGTTACAAAAAC | 114792 |
| rs549353492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985367 | GGAGTTGCTCTTCTC[A/G]AGGAGTATCTTTGTG | 114792 |
| rs549371709 | snp | A/C | 0.000164867 | 0.00907779 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114349 | GGGTGCCATGGAGGA[A/C]TACCTCTATGCAGTT | 114792 |
| rs549373172 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962324 | ACCAGAAATGGAGAA[C/T]GTTCCACTAATGAAT | 114792 |
| rs549376546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050606 | AATAACAAAAATAGG[A/G]GCAGACTCTATTACA | 114792 |
| rs549395058 | in-del | -/CTTTTTTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056106 | TTTTTCTTTTTTTTT[-/CTTTTTTTT]TTTTTTTTTGAGATG | 114792 |
| rs549416449 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043055 | GCACATGCCAGCTCC[G/T]CTTCTCCTCTGCCAT | 114792 |
| rs549416553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913175 | GCCTTTTTGACAGTA[C/T]TGTCCAGTTTAGGTA | 114792 |
| rs549433125 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061992 | TTTCTTTCTCCAACC[C/T]TTTAAGAGCACTTAG | 114792 |
| rs549434319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017062 | AGGTATTTCTTTATA[A/G]CAGTGTGAAAATGGA | 114792 |
| rs549438602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009443 | TCTTCACTATCGACA[C/T]TTTAGGATTTACTGG | 114792 |
| rs549439506 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964601 | GAGCTTGCAGTGAGC[A/C]GAGATCGCCCCACTG | 114792 |
| rs549443684 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954994 | ATGCTGCCAGATTCA[A/G]TGTCTGGGGAAGACC | 114792 |
| rs549454428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956839 | AACAGTGTTTCCCCA[C/G]TTCTAATGTTTCTTG | 114792 |
| rs549477319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010184 | TATTTATAGGACACT[A/C]TATGCCATGCTCCTG | 114792 |
| rs549483827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072069 | GCCTAGTCTACACTT[C/T]GGCTTGGGTATTTCT | 114792 |
| rs549491062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948716 | AAAATTAGGATTGAT[A/G]AAGGAGGGATTTAAC | 114792 |
| rs549494031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023930 | AAGCAATTGTGACTT[C/T]TGAAAAATGTGTGAA | 114792 |
| rs549503575 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913994 | AGGGGACTCAACGTA[A/C]TGAGAACCGTCCTTA | 114792 |
| rs549509190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136762 | GAGTGTTTTGGAGAA[A/C]AACTGCCAATGCTTC | 114792 |
| rs549516203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914833 | CCCCACCTAGGCAAC[C/G]TGGTGGTTCCCTGTT | 114792 |
| rs549516708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107177 | AGGTGCCTGTAGTCC[C/T]AGCTACTCGGGAGGC | 114792 |
| rs549539793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044151 | ATGGCCTTTATTGTA[C/T]TGATATACATTCTTT | 114792 |
| rs549541965 | snp | C/T | 0.000741577 | 0.0192416 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085265 | CAGAAGAAGTTCTAA[C/T]GCTTCCCTATTGCCT | 114792 |
| rs549544527 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991003 | GTTACTAATGGGAAT[A/G]TTTAATCGGGGCTTG | 114792 |
| rs549577782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100134 | GTGACAGAGTGAGAC[G/T]CTATCTCAAAAAATA | 114792 |
| rs549583747 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045074 | TGGAGTTAGTAGAAT[G/T]TAAGATATGTGTCTT | 114792 |
| rs549588310 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929854 | CATATGGCAGAAAGC[A/G]TTGAAAGCTGTAAAT | 114792 |
| rs549602191 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973967 | CCTCAAGTGATCCAC[C/T]TGCCTCAGCCTGCCA | 114792 |
| rs549611666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030387 | TTTGCATCACTTCTG[A/T]GTGAAATAAAGAGGG | 114792 |
| rs549623204 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063176 | GGAGAAAGCAGTGCA[A/C]CTAGCTAGGAGGTGA | 114792 |
| rs549623402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941573 | GAGGTTTGATATGAT[A/G]TGATGACCAAAAAAC | 114792 |
| rs549632123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985736 | ATCAGGTCCTTTAAG[G/T]ACTTCTCTAGAATTG | 114792 |
| rs549647797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070768 | TCTTAAAAATGAAGT[A/G]TTTCCAGGATTTTAT | 114792 |
| rs549658913 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037738 | CACCCTGAGCAAAAA[A/G]AACAAAGACATTACA | 114792 |
| rs549660104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935002 | ATATTAGGCATTTTG[A/G]AGAGATATGCAATTG | 114792 |
| rs549662013 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030964 | GAATCTGGGAGCACC[A/G]CAGTGAGAAAAGGAG | 114792 |
| rs549680273 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981008 | GCAAAGTGGTGGGGC[A/G/T]GGGGGGCAGGCGGGG | 114792 |
| rs549690687 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111032 | CACAGAAAAGTCTTG[G/T]GGGGGGGGGGTCTTA | 114792 |
| rs549695742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907898 | AACTAATAGCTCTTC[C/T]TTGTATGTGAATGAC | 114792 |
| rs549700381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101714 | ACTGAGTTTATTTGT[A/G]TGAAATATGGTTAAT | 114792 |
| rs549709198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071374 | TCGGGGCTCTCTCCT[A/T]TTCTCCTCCTACTCA | 114792 |
| rs549719302 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083262 | GGGTGCGATGGCACG[C/T]GCCTGTGGTCCCAGC | 114792 |
| rs549727494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052762 | AAATATTTTAAATTT[C/T]ATACCTAGATCAAGC | 114792 |
| rs549741945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004011 | GTTATTTCTAATTCT[A/G]TGAAGAATGCTATTG | 114792 |
| rs549775274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011426 | ACAATTATTAATTAC[C/T]AATCACAAGTATGTG | 114792 |
| rs549786504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943431 | ACCAAGGAGATTTCT[C/T]ACCCACACACAGGCT | 114792 |
| rs549787069 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045790 | GAAATGTGAACTGAA[A/G]TGAAGATAGCAGAAA | 114792 |
| rs549792972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129699 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT | 114792 |
| rs549815976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107670 | GGGCTTATGAATCTA[A/C]GTTTAGGGCACTGTA | 114792 |
| rs549821072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032678 | GGCAATTACAACTTG[C/G]AAGATCTGAAAAAAG | 114792 |
| rs549825194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937231 | CCATTTGCAGTTATT[C/T]GCCACCCCCTCTCCA | 114792 |
| rs549836787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065128 | AAGATTTCAGTAACA[G/T]TATCTAGTAAATCAC | 114792 |
| rs549842269 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951011 | AACAAAAAAAAAGTA[C/G]TTCTCACAAAACGTG | 114792 |
| rs549854092 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975225 | GGGGTAAGTTTCACA[A/G]TGTGTGAGGTTAGCA | 114792 |
| rs549874433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065952 | TTCTTATGATTATTT[G/T]AGCACATTTAATCTA | 114792 |
| rs549895197 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899142 | CTCTAATTTAAATGC[C/T]CTTTATTTAATTATA | 114792 |
| rs549930839 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966870 | TTGTGTCAGAACGTT[C/T]TATGTGGACAGTAAA | 114792 |
| rs549935780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066385 | TCCATGGGTATTTTC[C/T]TCTATCCCATCAGAT | 114792 |
| rs549946925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003423 | ATATAGTTTATAAAA[A/T]TTTTCTCCCATTCTC | 114792 |
| rs549954606 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080781 | GACAAGCACATTATA[A/C]ACAAGTAGGCAAATA | 114792 |
| rs549968345 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945202 | ATCATTTAATCCTAG[C/T]ACATGGCTGTGCCAG | 114792 |
| rs549983619 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996568 | GACACTGAATGAATT[C/T]GTAGTCTGGCAGGAG | 114792 |
| rs549989328 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133641 | AAAATTGCTAGCATA[A/T]AGTTGTTGTGTTATC | 114792 |
| rs549994832 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060343 | AAATAAAGAGAAAAA[A/G]AAGACAGAATTGAGA | 114792 |
| rs550001040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950394 | ACATGAAGCTCAACC[C/T]AGCTGAAGGAACTTC | 114792 |
| rs550021251 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127853 | ATCTAGGACAAGTCT[A/C]AAGTAGAAGTATATG | 114792 |
| rs550022378 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142205 | TATAATTTTATCATA[C/T]GCACAAATAACTCAT | 114792 |
| rs550023212 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053064 | ATTGTGACCCACTTA[C/T]AATAGTTATGAGGAT | 114792 |
| rs550034446 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004274 | TGATTTGGCTTTCAG[A/C]TTGGACGTTGTTGGT | 114792 |
| rs550036047 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025749 | GACTCTCCCTCTTAC[-/G]CAGCTTTATCGCCTT | 114792 |
| rs550050541 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100376 | TTGCAGCTCACTGAC[A/G]GTGTAGACCCTGGCT | 114792 |
| rs550070895 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931592 | TATTTCAATATTTCT[A/G]AAGATATAGTGCAAT | 114792 |
| rs550072958 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982595 | TGAAGAGGTCCTTCA[C/T]ATCCCTTGTAAGTTG | 114792 |
| rs550080624 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898095 | TTTAACGCTGGAACT[A/C]CGAGGGAGTCACCCG | 114792 |
| rs550090375 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968391 | AAACAAAAACAAAAA[A/C]AAAAAAAAAAACATC | 114792 |
| rs550091867 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018605 | GACTCAGTCTCAAAA[A/G]AAAAAAAAAATCAAT | 114792 |
| rs550094783 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111354 | CTCCCAGAGGAAGAT[A/C]CTGGGCGGGCCTCCA | 114792 |
| rs550102705 | in-del | -/CTGTGT | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949198 | ATGTCTTGTTTTAAA[-/CTGTGT]CTTCTAAAGGTAATG | 114792 |
| rs550122034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087281 | TCAAATCAGACCGCT[A/G]TTTTGCCTCAAGTAT | 114792 |
| rs550132937 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081219 | ATCTGCAGGAAGGAA[G/T]TGGGCAAAGCAGGGT | 114792 |
| rs550134016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080197 | TACCAATTTTCCCAC[A/G]CAGAAAACAGGATGA | 114792 |
| rs550158714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990750 | TGTGTTATGGGCCCA[A/G]GCTGGGGTGGGGGCG | 114792 |
| rs550164429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123045 | CTGTCCTGGTAGTGC[A/G]TTAGCACTGCATTAC | 114792 |
| rs550168375 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130579 | AATATGTGGCTCTTT[G/T]GTACTTGTTCTCATG | 114792 |
| rs550168650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032014 | TTTAAACCTATAACA[A/G]CCCTGTGAAGTTGGT | 114792 |
| rs550182038 | snp | G/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924557 | AAAGGATGTGCGCGG[G/T]ATCGCGGGGGAGGGG | 114792 |
| rs550197368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073299 | CCACTTCTCTTTGAT[C/T]TTGCTGAAATGCATA | 114792 |
| rs550207385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025225 | AATCTGATTTGGAAC[A/G]AATTGTCCATAGAGT | 114792 |
| rs550227887 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982149 | AATAGTATCAGTGAG[G/T]TGTTGAAGTCTCCCA | 114792 |
| rs550235283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103387 | CCTGGGTAATTTTTT[G/T]TATTTTTGGTAGAGA | 114792 |
| rs550267523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054724 | GAATAGACAGATATA[A/G]CACCTTAAAAACTAA | 114792 |
| rs550312875 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923936 | GACCTGAATGACTCG[A/G]AAGTGGCACTTGAGT | 114792 |
| rs550326647 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116026 | AATAACCAGGAAGAT[A/G]GTCACAGGCTCAGCT | 114792 |
| rs550342758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999203 | GAGTTCAAGACCAGC[C/T]TATGCGACATAGGGA | 114792 |
| rs550344440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018018 | TATAAAACTGCCTAA[G/T]ATTTTAATGCCACAT | 114792 |
| rs550361663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103103 | TTATATATAAATAAA[C/T]GTATATAAATGTAAA | 114792 |
| rs550394691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940430 | GAAGCCAATGCAGTG[A/G]TGTGATTCAAGGAGA | 114792 |
| rs550401501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109599 | CTTGTGTGCTTCTCA[C/T]GCAGTTAGTAACACT | 114792 |
| rs550409089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987336 | TCTCCTGCTTTCTCT[C/T]GTGGGCATTTAGTGG | 114792 |
| rs550432977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901314 | GTCAGCAGAGATATA[C/T]TCCTCCTGGATGCCT | 114792 |
| rs550437572 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057333 | GGACTACAGGCACGC[A/G]CCACCATGCCCGGCT | 114792 |
| rs550443478 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053728 | ACATTTGTTTTTTTT[A/T]ATTTATATACTATGC | 114792 |
| rs550459975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005390 | TCTTTATTAATCTAG[A/G]TAGTGGTCTATCTCT | 114792 |
| rs550480647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095468 | TTAATTCCACACCCC[C/T]TGGATTCTGGGAGTT | 114792 |
| rs550501045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916871 | TTTTGGTGCTCATCA[C/T]AAAGGAACTGTTTTT | 114792 |
| rs550501974 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118607 | CTGGGCAAGAAAAGC[A/G]AAACTGCATCTCAAA | 114792 |
| rs550509436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046907 | CAGGGTTAACATCGA[G/T]TGTATCTGCCTATAG | 114792 |
| rs550547275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075657 | ACCTTACCGCACATC[C/T]ACACCAGCCCCCTTT | 114792 |
| rs550556269 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006323 | TGCCTGATACTAGAA[-/T]TAGAAAGCTCTGCTC | 114792 |
| rs550568496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900409 | GAGATTACGGTAAGA[C/T]TCATGTTCTTCAATA | 114792 |
| rs550573860 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061128 | CCTGGAGGTCAGGCG[A/G]GGAAAGAATCCTCTA | 114792 |
| rs550574423 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974012 | CAGGCATGAGCCACC[A/G]TACCTGACTTCTTCT | 114792 |
| rs550608438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068325 | AGAACCATCATGTAG[A/G]CTTTTCAAATAAAAC | 114792 |
| rs550619826 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140358 | CCTAGAATTGGCAGT[G/T]CTAATAAAAGTTTTT | 114792 |
| rs550632656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014271 | CTGCACTCCAACCTG[A/G]GTGACAGAGCGAGAC | 114792 |
| rs550634892 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054885 | CAGAGGATGCATTGG[G/T]CTGATATCGTGCCAC | 114792 |
| rs550635711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132592 | CTCAGTGGCAAAAGG[C/G]TTAATTAAAATATGT | 114792 |
| rs550638245 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948899 | ATGCGAAAAAGTCAT[G/T]TAGCAATTCAAACAT | 114792 |
| rs550643218 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019776 | GAAACAGCAAAAAAA[A/T]TTTTATACTATTTTC | 114792 |
| rs550656832 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072938 | CTCTTTGCCCCCCAA[C/T]TCCTCATCTGTGAAA | 114792 |
| rs550665682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977545 | ATCTCCATATAAATG[G/T]GAATATAAACAATTT | 114792 |
| rs550678971 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040640 | TACACTTTGAGAACA[A/G]CTGAAACGGAGTGTG | 114792 |
| rs550681401 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141132 | TGGGACATGAATTTT[C/G]TCTCTAGCAGTTTTA | 114792 |
| rs550696742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911139 | CAGAACTTTATTCTC[C/T]CATAGTTCTGGAGGC | 114792 |
| rs550696907 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035728 | TGGTTCCCTTATACA[G/T]GACAAGTCACTTTTC | 114792 |
| rs550701369 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951731 | GTATACCTTGTGAGA[G/T]AAGTTTTATATATTT | 114792 |
| rs550714313 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911759 | TACTCAGCAGTATTT[G/T]ACAAAATTGGCCATG | 114792 |
| rs550722031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918239 | AGGGTGAGTTAACAG[A/C]GCTCATAGGTAAAAT | 114792 |
| rs550729030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945808 | CATGAACCTGGGCCC[C/T]GTTGGTGTCTACATC | 114792 |
| rs550733112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075195 | GGCCTTGCAAGACTC[C/T]AAAAATTAGAGCATG | 114792 |
| rs550790640 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983374 | TGCCAGGCTTTGGTA[G/T]CAGGATGATGCTGGC | 114792 |
| rs550805216 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058860 | CTAATCCAAATGTTA[C/T]TGGAAAAGTAACCCT | 114792 |
| rs550826422 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097546 | CACACTCTGGAAATC[A/C]CATTTTATTTTTTCC | 114792 |
| rs550853398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035081 | CTTCCTTTGTTATCT[A/G]ATTATTTTTGTAGTA | 114792 |
| rs550891711 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013478 | AATAGTTACACCAAT[G/T]CTAGGTGGTGTTTTT | 114792 |
| rs550914373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042087 | CCTAATACATTAATG[A/G]CCAAAGTTGTTATAG | 114792 |
| rs550926155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068975 | TGGGATGTGAGAGGC[G/T]GGGACGCAAGGGCGA | 114792 |
| rs550930268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993767 | ATAATGGCAGTAGTA[A/G]TCAAGTCTCAGCATT | 114792 |
| rs550936164 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020497 | TTGTCAGAAAGGCAA[C/T]GGGCCTAGATTTTTT | 114792 |
| rs550943762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933340 | CCTGTGATTGCTTCA[G/T]AATTCCGTTGCCATC | 114792 |
| rs550978185 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029070 | CAACTGCATGGTGAG[C/T]AGCAGTTTCTGGCCT | 114792 |
| rs551025720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061989 | GGGTTTCTTTCTCCA[A/C]CCCTTTAAGAGCACT | 114792 |
| rs551038928 | snp | C/T | 3.2987e-05 | 0.00406108 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127401 | CATGTTAATCCATTA[C/T]AGGTGGAGTAACTAA | 114792 |
| rs551058793 | snp | A/C/T | 5.53851e-05 | 0.00526213 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114614 | AATTGAAAGATTGAA[A/C/T]CAAGCATGCCATTTT | 114792 |
| rs551063649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934876 | TTAACAGGTTAGTAG[G/T]GAACTGCTGCAGGAT | 114792 |
| rs551073756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077332 | ATTTGTGACAAAAGA[C/G]TCTCAAAGTTCTGCT | 114792 |
| rs551086179 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056395 | CAAACGTGAGCCACC[A/G]GGCCCGGCCCACCAG | 114792 |
| rs551089056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056191 | GCTCACTGGAAGCTC[C/T]GCTTCCCGGGTTCAC | 114792 |
| rs551093368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919056 | CTCCCTGTCTCAGCA[C/T]AGTGAGAGATTCATG | 114792 |
| rs551097971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119420 | CAAGAGAGATGGATA[A/G]GAGTTTGTCTGGAAA | 114792 |
| rs551135389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063706 | AAACTTACTGATTCA[A/G]TATGTCTGGGAGGCT | 114792 |
| rs551146631 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098306 | TATGCATAGTGGTCT[C/T]ATCATATATTAGGCA | 114792 |
| rs551165470 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978929 | TTATATGCTTGTTGG[C/G]TGCATGTATGTCTTT | 114792 |
| rs551171754 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022832 | CTGCTATAAAGAAAT[A/G]CCTGAGACTGGGTAA | 114792 |
| rs551175916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049792 | GCCTTGGGGTAGATT[C/T]TCTCTTTTATCAGTG | 114792 |
| rs551189825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090549 | ATCCCTTTACAGTTG[G/T]AAAGTAGAAGACACT | 114792 |
| rs551207308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927305 | AATGGAGCATCCTGA[A/G]CCTTTAATGAAAATG | 114792 |
| rs551208233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954936 | AGCTTAAACAACAAG[C/T]ATATTTCTCACAATT | 114792 |
| rs551246999 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955847 | GAGGCTGAGGCAGGA[A/C/G]AATTGCTTGAACCTG | 114792 |
| rs551247215 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920071 | GTTTCAGGGAAAAAA[A/C]CCCGATGAGGAAGAG | 114792 |
| rs551253001 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091196 | CCTGGGCAATAGAGC[A/G]AGACCCTGTCTGGAA | 114792 |
| rs551260754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057664 | GCAGATGTATCTGTT[A/G]CAAATATTTTCTCTT | 114792 |
| rs551263347 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989720 | CTTTTTCTCCCCCCC[-/T]CTCTTCCAGGGATAC | 114792 |
| rs551268836 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929791 | TAAACGAACTATGTA[-/G]GAAAAAAAACAGTTT | 114792 |
| rs551320399 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988193 | GGGAGAAAATTTGTG[A/C/T]AATCTACTCATCTGA | 114792 |
| rs551343577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099359 | TTTTTCCTCTTCAGT[A/G]TGGCCTTCTCTATCT | 114792 |
| rs551357169 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988777 | TACTATGCAACCATA[A/T]AAAAGGATGAGTTCA | 114792 |
| rs551370771 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075964 | TAGATTTGCACAGCG[C/G]GGTCTTGATAATCTG | 114792 |
| rs551403903 | snp | C/T | 0.000429015 | 0.0146398 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085317 | CGACCGCCTGACCTC[C/T]CTGAGTGAAGAGCAG | 114792 |
| rs551404704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092240 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 114792 |
| rs551427612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120368 | AGGGCCTGAGGAGAG[G/T]GACCTTGGAATAAGC | 114792 |
| rs551434741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984863 | AATTGGAGCATTTAG[C/T]CCATTTACATTTAAG | 114792 |
| rs551463768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070608 | GATTGACTGTATCTT[C/T]GTTTGTGAGGATTTT | 114792 |
| rs551467892 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941145 | TCAAGGGTTTGTTTA[C/T]AAGGTTGAAATTTTA | 114792 |
| rs551479192 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985218 | ACTCTCTTCTGGCTT[C/G]TAGAGTTTCTGCCAA | 114792 |
| rs551482597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913855 | GGTGGGCAGATGTCC[A/G]TGTGCTAATTCTTAA | 114792 |
| rs551502819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948835 | CTCACCCAAGCCTAT[C/T]GACTGAGCCAAGAAA | 114792 |
| rs551519264 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111760 | CAAACAAGATGAAGA[C/T]GGTAAATGTGGGGGA | 114792 |
| rs551519671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979703 | TCTGTGAAAAACATC[A/G]TTGGTAGTTTGATAG | 114792 |
| rs551534711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112725 | GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCT | 114792 |
| rs551541363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079420 | CTAACTGCTCGATAA[C/T]TGCCTTGCAAATGTA | 114792 |
| rs551554229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972068 | TGTTGGCCAGGCTGG[C/T]CTTGAACTCCTGACC | 114792 |
| rs551567060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129146 | CAAATCACTTCTTTT[C/T]TTGAGTGTATCTTTA | 114792 |
| rs551595503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106571 | AACATGGTGAAACCC[C/T]GTTTCTACTAAAAAT | 114792 |
| rs551625287 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053063 | CATTGTGACCCACTT[A/G]TAATAGTTATGAGGA | 114792 |
| rs551627441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121127 | TGTTGATTTACCCTC[A/C]CATCACTGCCCAGGA | 114792 |
| rs551630325 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933274 | CCTTTTGGGCACTGT[A/G]TTCTTGGAATTCTGC | 114792 |
| rs551649859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071471 | GCATGGGCACCCTTC[C/T]CTTCTGCTCACTATC | 114792 |
| rs551654433 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141598 | TCAAATATACATTTT[C/T]GATTTAAGTGAACTA | 114792 |
| rs551659312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107058 | AGCACTTTGGGAGGC[A/G]AAGGCGGGCGGATCA | 114792 |
| rs551672951 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087580 | GCAAAAGGTGTTGGG[G/T]AGGAGAAAGGAAATT | 114792 |
| rs551673839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099925 | GAGGGTATCTTCTTC[A/G]ATAAAAATATTATTT | 114792 |
| rs551688386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913299 | TATGGTCTATCTGGT[A/C]TTGGCATTTGTCTGG | 114792 |
| rs551689808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107861 | AAATAGCCTAAAAAC[C/T]GAATTTTCCATTTAT | 114792 |
| rs551692304 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138249 | GCTGTGCTATATAAG[-/A]AGAGAGAGGCCAGGC | 114792 |
| rs551703756 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009273 | AAGAAACAGTATTTT[A/T]AAGGCTATTCAGCAG | 114792 |
| rs551706567 | in-del | -/TGT | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141816 | AACAGATATTCTTGG[-/TGT]TGTTAAAGGAAAAGC | 114792 |
| rs551731343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010298 | GCAGCAGTGGTGCTT[G/T]GCTCTGGTAGGGCTG | 114792 |
| rs551732963 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058515 | CTCTTTTTTCTTTAT[A/T]TAGAACTCTAATTTG | 114792 |
| rs551774803 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044263 | TCGTATGGTTGTTAT[A/C]TGTCATTCTGTTAAT | 114792 |
| rs551798072 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905156 | GCCCCAGCTACAGAA[A/G]GTAGTCTTGATAATT | 114792 |
| rs551807365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949394 | CACACTTGTTATCAT[C/T]GTTCATTTACCCAGA | 114792 |
| rs551808511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906127 | TCTGTTGGATGTGAC[A/G]CTGTTAGGTGAGGCA | 114792 |
| rs551813804 | in-del | -/GGTT | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007633 | TTTCTTCAGTCTTCA[-/GGTT]GCTGTCCTTTGGATG | 114792 |
| rs551814920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101946 | TGGGGAATACCTTCA[C/T]CTCTTGGAGGCATAT | 114792 |
| rs551819181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011185 | AGTTCACGTTAAATT[A/C]TACTAGGTTAGCACT | 114792 |
| rs551819236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003543 | GCAATTGCTTTCGGC[A/G]TCTTTGTCATGAAAT | 114792 |
| rs551850415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086434 | ATTAAAGAGCTGCAG[C/T]GTCCTGAAGGCCTTC | 114792 |
| rs551871566 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956520 | TGTGTTGTGCTTCTC[A/G]TTTGGAAAGCTTTCT | 114792 |
| rs551876579 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897472 | AGGCGGGGCCGCCGA[C/T]CTCACCGCGGGCGCG | 114792 |
| rs551886122 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066670 | GTATCAAAATCATGT[C/T]GACGTAGAAACCTTC | 114792 |
| rs551887913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044491 | AGTGTCTTTGTCTGG[C/T]TTTGGTATCAGAATA | 114792 |
| rs551888923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975087 | ATAGCTGTCTGTAAA[C/G]TGAAAGTTTGCATTT | 114792 |
| rs551890161 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907328 | CTAGTCATTATTTTT[A/T]AAAAATCCTTCTTTT | 114792 |
| rs551894988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036754 | ATCACACCCAGGTGT[A/G]GGCTCATGTGAAGCC | 114792 |
| rs551910421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138855 | AAATGAAGTAATGCT[A/G]CCTACCTCATAATTG | 114792 |
| rs551917148 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921176 | TATTTAATTATGTAA[C/T]TACGATATTCTTTCT | 114792 |
| rs551931741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030460 | TTAAAGTGGATTATA[C/T]ACTCACAAACTAGGT | 114792 |
| rs551953519 | in-del | -/T | 0.0185938 | 0.0946107 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978909 | AGTAATGTTGAGCAC[-/T]TTTTTTATATGCTTG | 114792 |
| rs551955055 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054455 | TCTCACAGTAGGTCA[A/G]ACTGTGATTGGAAAT | 114792 |
| rs551961503 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899271 | CTGCTCCAAGATTTC[C/T]ATCTTTGATACTTTT | 114792 |
| rs551980042 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918222 | TCCTAGCAAGGATGC[A/G]TAGGGTGAGTTAACA | 114792 |
| rs551982663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935663 | GCCTTGGGCACAGCT[A/G]CTGAGTCTAATGTGT | 114792 |
| rs552006197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024261 | TAGATATTCGATAAG[C/T]ATTAATTGCCTGGCT | 114792 |
| rs552014271 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020836 | TCTGAACCTTCCTTG[-/C]TAGTTTTTCCCAATC | 114792 |
| rs552021257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031148 | GTTTGGATAGACTAG[A/G]CAACTGGTGTTTCAC | 114792 |
| rs552023959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915649 | TAAGTTTCTATCCAT[A/G]GAGTAAAAAAAAAAA | 114792 |
| rs552035161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131501 | CCACAGAGCAACATT[A/G]GGTATGGACCTTCCT | 114792 |
| rs552041462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032159 | CCTGCATAGTTCTGA[A/G]CATTAAAAATAAAGT | 114792 |
| rs552061265 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065154 | ATCACAAAGTCCTAT[G/T]TAATTAATTACCATG | 114792 |
| rs552079824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032808 | TTCAGAAGCAAATTC[A/G]ACATTTTATAAACTA | 114792 |
| rs552087030 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929358 | AGGAGCCCATCTTTC[G/T]TAATAAGCAAGGGGC | 114792 |
| rs552105613 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033086 | TAAATTTTACTAAGA[A/G]CTTGCCATATGTCAG | 114792 |
| rs552109790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046740 | CTGCTTTCTCTTACT[A/G]TGGAGTCGACATTAA | 114792 |
| rs552112748 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922814 | TTTGTGTTGAATTTT[A/G]GTGGCTATTGAATAA | 114792 |
| rs552128632 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902422 | GTGTCTGGGCATGTT[A/C]TTTGCATACTTTTTA | 114792 |
| rs552130185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088002 | TGTTCTTTTTTTTCC[A/G]TCTGACCTTTCTAAG | 114792 |
| rs552141849 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060947 | TCGTGGCCCTCTCCT[C/T]ATTCATATGACCTTG | 114792 |
| rs552144503 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025785 | GTTTGCTTAATTTCA[C/T]TGGGTCTCATTTTCT | 114792 |
| rs552150243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929938 | TAATTTTTAAATGAA[A/G]AAGAAATGTCTTTGG | 114792 |
| rs552167861 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026063 | GGTAATATGTAAAAT[A/G]TAATTATATAAATTT | 114792 |
| rs552173339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039406 | AAGGGTCGTAGGGAG[C/G]GGGAGGATGATGGGG | 114792 |
| rs552200843 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030812 | ACACCTTACATGCAG[A/G]ACATTTCTGTTACAT | 114792 |
| rs552267544 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938101 | CAAACAGAAAAACCC[A/T]TAAAGCCCCTAGGAG | 114792 |
| rs552277882 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945752 | GGGTGGTAGCTTCCC[A/G]GGGGAGTCACAGGCT | 114792 |
| rs552279951 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96999502 | CATCTGTTTTCACCA[C/T]ATTTGATGGAATTTT | 114792 |
| rs552292780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958899 | GCCTCAGGGATGGAG[A/T]GTTGGGAGGTGATGG | 114792 |
| rs552295771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124702 | GTGGAGCTTTGCCCT[C/T]GGTTCCATTTCAGTT | 114792 |
| rs552300299 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924843 | CACACACACTTTCGC[A/C]CACACAAACACGCTA | 114792 |
| rs552311440 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909611 | GATAGGGGAAACTTT[A/G]CCTAAGATGCTACAG | 114792 |
| rs552328108 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087451 | CAGGCTGGAGACAGA[G/T]CTACAGAATCTCATT | 114792 |
| rs552365152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117186 | GGTATAGTTCACCCT[A/G]CCTATCACTGAGTTG | 114792 |
| rs552367981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054824 | ACAGCCTGTACTCCC[A/G]GCTATTCGGGAGGTT | 114792 |
| rs552376906 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990798 | AGCAGGGAGCATTGG[A/G]GGCTCATAGGTGAGC | 114792 |
| rs552417907 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951213 | CTGAGTAGGACAGGG[A/G]AGAAGCCAGGACCAG | 114792 |
| rs552447689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060876 | ATACAGCCACTGGTC[A/G]GTTCTTATCCCCACC | 114792 |
| rs552448287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960999 | AAGAATAGATTGTAA[A/G]TCAGTTGTCTCCTGG | 114792 |
| rs552450045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055655 | ATACAAAAATTAACC[A/G]GGTGTGGTGACATGT | 114792 |
| rs552485014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953223 | AAGAATCTATCAATA[A/G]TGTATGTGAGAACTT | 114792 |
| rs552487504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937317 | TGGCATATTTGTCTT[A/G]TTTGCTTAGTGCTTA | 114792 |
| rs552506851 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968400 | CAAAAACAAAAAAAA[A/C]AACATCTAGCCCAAA | 114792 |
| rs552522873 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986365 | TCTTAGATGTCCAAC[G/T]GCATGCTGGGAGAAC | 114792 |
| rs552527983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074563 | GTCTCACTCTTATTC[A/G]TAATAATGATTAAGA | 114792 |
| rs552531741 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081843 | TGCTTATCTGTGTTG[A/C]CAATTCCTGCTGTAG | 114792 |
| rs552567066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986678 | CTCCAAGCAATGCAC[A/G]GGATATAATCTCCTG | 114792 |
| rs552569849 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066652 | GAAATTTTGACTATA[C/T]GAGTATCAAAATCAT | 114792 |
| rs552571174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074145 | TTCACTGAAATGCAT[A/G]CTCCAGAGTAATGAT | 114792 |
| rs552583012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982830 | GTCATCTGCAAACAG[A/G]GACAATTTGACTTCC | 114792 |
| rs552598248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018462 | TCTGGGCGTGTTGGC[A/G]CACTCCTGTGATCCC | 114792 |
| rs552616736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096682 | TACCAATTGTGGTTC[C/T]CACCATAGCATCAAG | 114792 |
| rs552633477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074864 | TATTTTCAATTAAAA[G/T]AAAATATATATATAT | 114792 |
| rs552673369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983404 | CCTCATAAAACGAGT[C/T]AGGGAGGATTCCCTC | 114792 |
| rs552690443 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986837 | GGTGAGACGATGCCT[C/T]GCCCTGCTTCAGCTC | 114792 |
| rs552691033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983084 | GTTGAGAGTTTTTAG[C/T]ATGAAGCGTTGTTGA | 114792 |
| rs552695652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916546 | GCCTTGTCACTTTCC[C/T]GTAATTTATCACCCT | 114792 |
| rs552700761 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974601 | CTGTCAAGTTTTTTC[-/T]TTCCATATTTCTGAC | 114792 |
| rs552711799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968073 | AAGTAATGAGACCAG[C/T]TTCTTTCCATGACTC | 114792 |
| rs552740170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110187 | CTCATTTCTTTTGCA[A/G]TATCTTTGATTATTG | 114792 |
| rs552778616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976685 | CTCACTGCAACCTCT[A/G]CTTCCTGGGTTCAAG | 114792 |
| rs552796168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096164 | AAATGGCATAAGTTT[C/T]ATATAAAAATTTTGA | 114792 |
| rs552800985 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903760 | ATTTGGTTAAATTCA[A/G]CACCCATTACTAAAA | 114792 |
| rs552801966 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006397 | TACTTTGAGCCTATC[A/G]GGGTTATTGCATGTG | 114792 |
| rs552822395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104263 | TGGAACTTACATGTG[A/G]CAGGTCTGAGGGTAG | 114792 |
| rs552833652 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040388 | AAATTTTCATTTGAC[A/T]TACTGATTTGCAGTA | 114792 |
| rs552839797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110425 | CACTTCCACGTTCAC[G/T]TCATTCAGAAAACTA | 114792 |
| rs552844503 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127920 | CATCTAACAGCTGGG[A/G]GTTGAATATGCATAT | 114792 |
| rs552855368 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954536 | GGTGTTGGCTTAGTT[A/G]TATTCCCCAGAGAGT | 114792 |
| rs552860828 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102952 | ATATTAAGCCTAGTA[A/C]TCAATAGTTATTTTT | 114792 |
| rs552861722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961757 | ATTGAGCTGTATGGT[C/T]CTTCATAGGATATAT | 114792 |
| rs552885949 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097070 | TAACTCTGCACTGTC[A/G]GAACTCATAATAAGT | 114792 |
| rs552887565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124353 | TCTAAACATTGTCAT[G/T]TGAGTGAAAATTTGT | 114792 |
| rs552890367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999416 | CAACAACAACAAAGA[A/G]TTAATTTCCGTTTTT | 114792 |
| rs552907111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013278 | GTGCACTGAGCTAGT[A/G]TTAAATAACTTTTTA | 114792 |
| rs552909511 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999219 | TATGCGACATAGGGA[C/T]ACCCCATCTCTACAA | 114792 |
| rs552934725 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930816 | GCTCCTGGAGCATCG[A/G]CCTGGTCACAAGGAA | 114792 |
| rs552941598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968736 | CAACCACATGCTCTG[A/C]TGTATCATCTCCTTG | 114792 |
| rs552951590 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035984 | TCGGTTTACTTGATA[C/T]TGTTCCATAAAATCC | 114792 |
| rs552961273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987103 | ATTCTTCTCTCTTTT[C/T]TTCTTTATTAGTCTT | 114792 |
| rs552971238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067137 | GTGCTCACTACAAAG[C/T]AGCTCCAAGGGAAAC | 114792 |
| rs552972111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902193 | GGTTGAACTAATTTA[C/T]ACTCCCACCAATAGT | 114792 |
| rs552976319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917554 | ACCATTTCTTGTTCA[A/G]TACCTCAAATGATCA | 114792 |
| rs552977661 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900531 | AAGGTTGGAATATGG[A/G]TGGGAATCATTAGTT | 114792 |
| rs552980168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133970 | TGTTTAGTATTATGT[A/G]TCTCTAATACAATGC | 114792 |
| rs552993798 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018941 | TCATATAGATTTTTT[G/T]AAATGTAGACGGAAG | 114792 |
| rs553005526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033671 | GATTCCCTTTTCTCT[A/G]CAACCTCACCAACAC | 114792 |
| rs553014257 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038561 | CTAGTACACTGTTGA[C/T]GGGAATAAATTAGTA | 114792 |
| rs553014474 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935611 | CCAGCCAAAATTATC[-/T]TTTTTGGCCATCTGT | 114792 |
| rs553026038 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125176 | ATAGTCCTCTAGTTA[A/G]TAATAGCCAAAGCCA | 114792 |
| rs553039705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910447 | TTGTGTATGAGCACT[C/T]TAATTTGTGTTTATT | 114792 |
| rs553043390 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126275 | GATTTCTTTGGTCCC[A/G]TATCCTTGATATTTT | 114792 |
| rs553053817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993905 | TCTTTTATAATGAGT[A/G]GCAAACATGTCTACC | 114792 |
| rs553080816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090163 | TAATAATAAATAAAA[A/G]CAACAATGTAGAGTT | 114792 |
| rs553093488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027023 | AAAAACCAGCTGGGC[A/G]TGGTGGCGTGCACCT | 114792 |
| rs553097568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932420 | TCATTTAAGAAACTC[A/G]TGCACAGCCCTTAGG | 114792 |
| rs553109713 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925156 | CCATGCAGCCTCTGC[A/C]CGTGTCGTCTAACGG | 114792 |
| rs553176154 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028615 | TTCCTTCGTGCAAGC[C/T]CCAAATTCTGTCTTA | 114792 |
| rs553178419 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113399 | CCTGAGCTTTGATGA[C/T]ACCTCCCACCATTGA | 114792 |
| rs553225782 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939704 | CTGGAGGACGGGTAG[A/G]GAAGGACTGCACACA | 114792 |
| rs553230523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055223 | ACCTCCAGTACACAT[A/G]TCATAAGGAAAAGTC | 114792 |
| rs553243698 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082486 | GGCATGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 114792 |
| rs553256280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927339 | GATTAAAGTGTTAGA[C/T]AATTAGGTAAAACCC | 114792 |
| rs553306423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962032 | TAGTTATGTATTTTT[C/T]GGTCATATAACTTGC | 114792 |
| rs553319637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919495 | TTGTTTGTTTTTGAA[C/T]CTTCTACTTCTACCA | 114792 |
| rs553350140 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092313 | TCATACATGCATGTG[-/T]TGTTACTATTATTTT | 114792 |
| rs553350648 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974589 | TATCATCACCGTCTG[C/T]CAAGTTTTTTCTTTC | 114792 |
| rs553362034 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142980 | TAAAGATATACAAGT[C/T]TTAAACTATGAAATT | 114792 |
| rs553384314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090738 | ATCTTCATTTATTAT[C/T]GCTTTGTTCTCCTGT | 114792 |
| rs553419395 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005075 | CAGCACTTTTTTGTA[C/T]ACCTGGTAGAATTTG | 114792 |
| rs553431752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920169 | CTCAGTAAGGGAACA[C/T]GGTCAGGGAAAGGGA | 114792 |
| rs553445348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970925 | TAATGTCTTTAATTT[C/T]CATGAAAAGATTTTG | 114792 |
| rs553447582 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082772 | ATGTGGGTCAGTCAT[A/T]TAGATGTGGAAGGCA | 114792 |
| rs553468228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035250 | AAATTCCACACTTTT[A/G]CCACCTCCCCCAAAC | 114792 |
| rs553471752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007677 | CTTTTTCATCTTTGA[A/T]ACCCTTGGGAGTTTG | 114792 |
| rs553497901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946740 | CAACTAGACCTAAGG[G/T]AGATCCTAATGAGAT | 114792 |
| rs553529506 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971256 | GTTTAAAACCATATA[A/G]CTGTTTTCGGAATTT | 114792 |
| rs553531238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963478 | TTCTTTACAAAAGGA[A/G]AACGGTACCCTGTGT | 114792 |
| rs553542760 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013128 | AATATAGTAAATGCT[C/T]TTAAAATAATTGTAC | 114792 |
| rs553574779 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098526 | TTCTATTTTCACATT[-/A]TTTTTTTCTTGCTTT | 114792 |
| rs553579143 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123422 | ATAGAAAGCATTTCT[C/T]ACTGTTGGTAGCATG | 114792 |
| rs553579510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076731 | TGCTAAAAGTAGCAC[A/G]CAGTTCTGAAAAGTT | 114792 |
| rs553599774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983990 | GTGTCAATTTTAGAT[C/T]TCTCCTGCTTTCTCT | 114792 |
| rs553622881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091541 | GTGGGGCTTTCCGCT[G/T]GCTGCTCTTTCCCAC | 114792 |
| rs553641794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069290 | TAAATTTTACACTAA[A/G]TGGGCTACAGTGAAA | 114792 |
| rs553646419 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132194 | GCCATTTGTCTTCAT[C/T]TGGGGCATGCTAGGG | 114792 |
| rs553650388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135566 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 114792 |
| rs553665268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078358 | CTATAGTAAAGTATC[A/G]ACATGGGGTAATTTA | 114792 |
| rs553667997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112113 | TGTTCTCACTTTGGG[C/T]TGCGGTGCCAGGCTT | 114792 |
| rs553691541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957256 | TCTGGATTACATCTA[G/T]ATCATAAATTTGGGA | 114792 |
| rs553693635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035970 | TTTCATAATCTATAT[C/T]GGTTTACTTGATATT | 114792 |
| rs553705886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905243 | CATTTTCATTTCAAA[G/T]ATTATGAAAGATTAT | 114792 |
| rs553713033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015612 | AAAGGGAAGGAGAGC[A/G]TAAAAGTTTGGAAAA | 114792 |
| rs553715911 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988985 | AGGAGGGATAGCATT[A/G]GGAGATATACCTAAT | 114792 |
| rs553728607 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070907 | TTTCATTTGAGATAT[G/T]TATTCTCCCACCCAC | 114792 |
| rs553740247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105353 | TGTTGCCCAAGAGCT[C/T]ATCAACATGCCCTGC | 114792 |
| rs553743752 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976255 | AACTGTCACTAAACC[A/G]GGAGCCAATTAGGTG | 114792 |
| rs553760621 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979095 | TTCCCCATTTTGTGG[A/G]GTGTGTTTGTTGATA | 114792 |
| rs553782045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980257 | GTTCTCAAAGGGAAT[A/G]CTCCAGCTTTTACCT | 114792 |
| rs553813042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964584 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 114792 |
| rs553839985 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953912 | TCAATCCTCAAACTC[C/T]CCTCTAGCTGTAAAT | 114792 |
| rs553848370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971662 | CCTATGTGGGGTCCT[A/G]TGAAATACAGGGACA | 114792 |
| rs553866476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098982 | GGATCTGTGACAATG[A/G]ATTATTTTATCTTAT | 114792 |
| rs553886460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904500 | TATGAAAGAACATAA[A/G]GAAACACACATGGCT | 114792 |
| rs553900945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030608 | GCATGAGTCTGTGCA[A/G]TGCTTTCATATTTCT | 114792 |
| rs553903324 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926768 | TAGCCGATTGTTACT[A/G]TCCAGGCTCTAAAAC | 114792 |
| rs553907965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973754 | TTTAGACAGAGTCTC[A/G]CTCTGTTGCCCAGGC | 114792 |
| rs553924842 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086015 | TGACTATTCCTTGAA[A/G]AATCCACTTGGTGTC | 114792 |
| rs553946349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099407 | CTTCCTCCTAATCTG[A/G]TAAAGAATGTTTCAG | 114792 |
| rs553983857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084836 | TCTAGAATGTTGCAA[A/G]GTAACATTTCAGCCC | 114792 |
| rs553989678 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910861 | AGCTTTGACACTCAA[A/G]GGAGTATTTTCCAGG | 114792 |
| rs554008085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101267 | ACATAGAAAGATGAT[C/T]CGTGTGCGTTTCTGA | 114792 |
| rs554008392 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093383 | AGTATGATCCAAATT[C/T]TAACTAGTGAGAAAA | 114792 |
| rs554024206 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896266 | ATTCCTAATGTATTC[G/T]TTGATCCTTCTAATT | 114792 |
| rs554040998 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017433 | TATAGTTTGAGGTTT[G/T]CTGGTAGCATTCCAT | 114792 |
| rs554053452 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985893 | AAGTCATTCTCCGTC[C/T]AGCTTTGTTCCATTG | 114792 |
| rs554066338 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938529 | TCCTCCCTGATGACC[-/T]AGTGGTATTAAGGCT | 114792 |
| rs554069732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093932 | CAGACTGTGTGGGAA[A/G]AAGTCTGTAGGCTGT | 114792 |
| rs554071904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030093 | TTCACCTGTAAGATT[A/G]TTTGTATTCTTGATA | 114792 |
| rs554075199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108041 | AGGGTGCTTGAGAGA[C/T]CTCCTGTTGTACATG | 114792 |
| rs554076577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995346 | TTTCATCCTTTCCCA[A/G]CTTTTCATTTCCTGA | 114792 |
| rs554094360 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897896 | TGCGCACAAGTGAGG[A/G]GAAGCCCCGCCGCGG | 114792 |
| rs554131987 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914688 | TTTCTTTTTCTTTTA[-/T]TTTTTTTTTTAGAGA | 114792 |
| rs554138902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996711 | CAAGCAATAACAATA[A/G]TAACTAATTAATATT | 114792 |
| rs554143999 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897065 | CCGACAAGCTGAGGC[A/T]ACAGGCGCGCCACCA | 114792 |
| rs554145185 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022615 | GCTGGGATTACAGGC[A/G]CCTGCCACCACACCT | 114792 |
| rs554150714 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045151 | AAAGGAAATAAGCCA[C/T]TAATCAAGTAGAAAG | 114792 |
| rs554152658 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967043 | TAAGGCTGAGAACCT[A/G]AGGAACCCAGCTGGA | 114792 |
| rs554158734 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120726 | TGGAGGCGGCCATGA[A/T]GTGAGGAAGCCACTT | 114792 |
| rs554175957 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990419 | TGCTTAAGTATAATG[G/T]TAAGTTCTTGCTCAA | 114792 |
| rs554177577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003673 | ATTTTTTGTATATAC[C/T]GTAAGGAAGGGGTCT | 114792 |
| rs554206675 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024292 | GACTATGAGCAGCCA[A/C]ATAGCTGCTGTAATA | 114792 |
| rs554215305 | snp | C/G/T | 6.82751e-05 | 0.00584241 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113765 | TGTCTCCTCTCATCT[C/G/T]ACTTCCCTCTGTTTC | 114792 |
| rs554230236 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124570 | GAGTCTGATACATAC[A/G]GTAGTGTAAGTATTT | 114792 |
| rs554238086 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108972 | AATAAATACAGCTTC[A/G]TAGAGTAACTAAATT | 114792 |
| rs554263659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990833 | CTGGCCTCTTCTCTT[C/T]AAGATGGCTGTGGTT | 114792 |
| rs554270759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023486 | ACAGAAGCTGCTGTG[C/G]GGGTGGGAAACACAA | 114792 |
| rs554294342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123289 | GTAGCAGAGACAAAG[G/T]TTGCTTGTTTGGCAG | 114792 |
| rs554299296 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928666 | TGTCTGATGGCTGGT[A/C]TATAATTTCCTCTCA | 114792 |
| rs554309125 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058122 | TCTCTCTTCTTTTGC[C/T]AATGTCACACTGTCT | 114792 |
| rs554311834 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921394 | ACACTGGCGCTGGCT[C/T]CTGATGAATAGGATG | 114792 |
| rs554330624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087526 | GTGCTCATTGACTTT[A/G]ACAAATCCCTATCCC | 114792 |
| rs554356536 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016696 | TTGAAGTGTGAGGAC[A/G]AGATTTGGGAGGGGC | 114792 |
| rs554363903 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025529 | CTCAGGTAGGCAATG[A/T]ATATTCATCCTTCTG | 114792 |
| rs554419212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116434 | TGGCAAAACAACGAT[A/G]GGTTTATGAAATCAA | 114792 |
| rs554424496 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986465 | GCTGTGCCCTGCCCC[C/G]AGAGGTGGAGTCTAC | 114792 |
| rs554432063 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958531 | AACCAGAAGAAGAAG[A/G]ATCAAGTGGTAAAAC | 114792 |
| rs554435658 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131880 | GTACCTTAGGCCCTC[A/G]ATTCTGGATCTGTGA | 114792 |
| rs554450509 | in-del | -/CATTTT | 0.00159617 | 0.0282053 | cds-indel, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141640 | TTCATCTTCCATTTC[-/CATTTT]TACTCTTCAAAATTA | 114792 |
| rs554465862 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982665 | TGGGAGTTCACTCAT[A/G]ATTTGGTTCTCTGTT | 114792 |
| rs554485768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914347 | AATCCTCTGTACTGG[C/T]TAAGTCCTTGCTTAA | 114792 |
| rs554490109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937568 | CCCCTCAGGGAGATG[A/T]GCTGACTCCTCACAC | 114792 |
| rs554491296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906724 | AGTAACCTAAATAGT[A/G]GGATTTGAGATTCAG | 114792 |
| rs554495996 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052450 | AAAAGCCAATGTATT[C/G]TGACACAGAACATCA | 114792 |
| rs554510590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982390 | GCTTTTTTCCATTTT[C/T]TGTTTGCTTGGTAGA | 114792 |
| rs554557719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931269 | ACCAGCAACTCCTTC[C/T]TCTGTGTTGAAATAT | 114792 |
| rs554559247 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045198 | AAGGTGATGGATCAC[A/G]AATTCAAGATTAGCC | 114792 |
| rs554565556 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973390 | AATTATCTTAATATA[G/T]TCTTCGGTTCCACTA | 114792 |
| rs554577588 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949907 | CTTAAATCAATATTG[A/T]TTTTTCTTTTTTAAT | 114792 |
| rs554583789 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045789 | TGAAATGTGAACTGA[A/G]GTGAAGATAGCAGAA | 114792 |
| rs554606641 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109692 | GGCATAGGAAGAGCT[G/T]ATTTATGAGGAGAGA | 114792 |
| rs554611688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079787 | ATTCCCTAAAGAACA[A/G]CAATGTATGCACCAT | 114792 |
| rs554629394 | in-del | -/CAGCCCTGTAC | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903006 | CCCTGTAGAATAGTT[-/CAGCCCTGTAC]TGAAGTCAGGTAGCA | 114792 |
| rs554655127 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999271 | ATGGTCACACGTGCC[-/T]TGTAGTCCTCGCTCC | 114792 |
| rs554656932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136077 | TGTCGTCAGTCACAA[A/G]TCTGTATATTTGATC | 114792 |
| rs554702714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942919 | AACCTGTTCACCTCT[C/G]TCTTGCCCACATGCC | 114792 |
| rs554705765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981704 | GTACTGTAAACTCCT[C/G]TCTTAACACTGCTTT | 114792 |
| rs554734987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005558 | CTTTTCCTATTTCTT[A/C]TAGGTGTGATATTAG | 114792 |
| rs554751159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960316 | CAATTCTCGTTTACC[A/G]TACTTTTCCTGGTCA | 114792 |
| rs554767136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115587 | ATCACACCCCTCTGG[A/G]CTGCCTTTTTGCTTA | 114792 |
| rs554828751 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140649 | CTCTTTTTTCCTTGG[C/T]AGTTTAATCATTCAG | 114792 |
| rs554836586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095009 | AGCATAATATCATTA[A/C]CTTTGATTAATTCAT | 114792 |
| rs554837325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952560 | TTTGAAGCAAGAATC[A/G]TAATAGCTACTCCCT | 114792 |
| rs554851821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066066 | TTTAATCCCTTTCTG[C/T]CTGTAGCAAATGGGA | 114792 |
| rs554854850 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920758 | TTTGACTGGTCCCCA[A/G]CTGATGGACCTTTAG | 114792 |
| rs554864410 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958008 | AGAATAATGGTAGTC[C/T]ATGAGGATTTAAAAC | 114792 |
| rs554881024 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042728 | GTGAAGTAGATCACT[A/G]CAGCTTATTCCTGCT | 114792 |
| rs554882781 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975617 | CACACACACATATAC[A/C]CATGCCCAGATGCAC | 114792 |
| rs554892393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132809 | AGGTTACATTTTGCA[A/G]TGCTGCTACTGAAGA | 114792 |
| rs554906049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066706 | TTCAGCCTTTAAAAA[A/G]TATATATACCCTGCT | 114792 |
| rs554918146 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959669 | CAAGACATGAATTGT[G/T]GGGGGACACAATTCA | 114792 |
| rs554924814 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081926 | AGGGTGGATAGGGTT[A/G]CTGCACCTTAGGATG | 114792 |
| rs554929891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067945 | GATATCCTCAGTGGC[A/G]GGCAGAGCCTCTCAG | 114792 |
| rs554952026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959757 | CTTGGCCTTTGGTTT[C/T]TATGGATCAGGAAGG | 114792 |
| rs554959897 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964782 | GTAAATAATATGTAG[C/T]AAAAATAGTAAATAT | 114792 |
| rs554967975 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068359 | CAAAGTACTGAATAC[A/G]CAACTCCCTTTTTGA | 114792 |
| rs554983865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987153 | TGTTGATCTTTTCAA[A/G]AAACCAGCTCCTGGA | 114792 |
| rs554984445 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977169 | AAGGATTTTATATGC[A/G]TATCTCATTTGATCC | 114792 |
| rs554992270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068473 | AATCAGAAAAAATAA[C/T]GAAAAGAAAAATTAT | 114792 |
| rs555016648 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983522 | TGCTGGACTTTATTT[G/T]GTTGGTAAGCTATTA | 114792 |
| rs555023076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908570 | TATCAAAAAGCAAGA[C/T]GAAAAGAGAAAAAGA | 114792 |
| rs555047262 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139970 | TTAAAAGAACATTAT[A/G]AGGATTAGGCGAACA | 114792 |
| rs555047800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968166 | GGTGTAACGCCTCTG[C/T]ACTCCCTATGTGAGT | 114792 |
| rs555051251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061632 | TCAGACTACATGTTG[A/T]TGGGTATGTTTCTGA | 114792 |
| rs555065432 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941750 | TGTCACATAGCTGCC[-/T]TTTTTTCTCTGATTT | 114792 |
| rs555082890 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993506 | GCTAATGTCCCCCCT[A/G]CTGGCCGAGCAAGTC | 114792 |
| rs555108604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969475 | CTCTCATTTCCTGTA[C/T]TTTTGATGCATTTGC | 114792 |
| rs555126856 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038381 | ATTTCTTAAAAGAAG[A/C]TATACAGATGTCCAA | 114792 |
| rs555142357 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081417 | TGGTTAGTTTGCATA[G/T]GAAAGCCGTTTGCTC | 114792 |
| rs555154965 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123470 | CTTCTGGCAGTTTTT[A/G]AAGACTTATTTGACT | 114792 |
| rs555157994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925795 | CATCAGTATTGAAGC[A/G]CAGTTTTTTGCACCT | 114792 |
| rs555178727 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979179 | TTTTGGTTTTGTTGG[A/C]ATTGCTTTTGGTGTC | 114792 |
| rs555178930 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986884 | ATCCACTGTCCTGCA[C/G]CCACTTCCTGACACT | 114792 |
| rs555187003 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904745 | TATATCAGAATATGA[C/T]ATAAAACTTTATGGT | 114792 |
| rs555195783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999281 | CGTGCCTGTAGTCCT[C/T]GCTCCTTGGGAGGCT | 114792 |
| rs555196069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991727 | GAGGGCTTCAGAGCA[C/G]CAAAAGTAGTAGCTT | 114792 |
| rs555211688 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071365 | CTCTCTTTCTCGGGG[C/T]TCTCTCCTATTCTCC | 114792 |
| rs555212840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090189 | GAGTTTCCATATTAA[A/G]ATGTATTGAATGGAT | 114792 |
| rs555213009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104537 | CTGAATATTGTTTTA[A/G]AAATCTGTCAGGTTT | 114792 |
| rs555225683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077234 | GGGAAGGGCATTTAT[A/G]TTACAGAACTTCCCC | 114792 |
| rs555250302 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103464 | GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 114792 |
| rs555257935 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918865 | AGAAAATATTAAAAG[A/G]AAGTAATAAAATTCC | 114792 |
| rs555290433 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052046 | CCTAAAATGAAATTC[A/C]TAGACAATATAACAT | 114792 |
| rs555328033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075749 | ATAATACCTTGATTT[A/C]TAACTCAGTTGTAAT | 114792 |
| rs555357127 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117628 | TACAGGCTCCTGTAG[C/T]GTTTGACATTGTGAC | 114792 |
| rs555362165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954384 | TGATGCTTAGATATT[C/T]ACTCATATTAAAGAG | 114792 |
| rs555367389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136489 | GAAATAGATTACTGA[C/T]GAAAGTGAAGGTGTT | 114792 |
| rs555376669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988281 | AAACAACCCCATCCA[C/G]AAGTGGGTGAAGGAT | 114792 |
| rs555383468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983910 | TCTTACTTATTTCTT[G/T]CCTTCTGCTAGCTTT | 114792 |
| rs555396263 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133506 | TTTATGGGAAGATTT[G/T]TAACAACTGCATCAA | 114792 |
| rs555413337 | in-del | -/C | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008883 | TTGATGGGAGATGTT[-/C]CTCCTGGCTGTGCTT | 114792 |
| rs555417273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902369 | ATATTGAGCTTTTTT[C/T]CATGTTTGTTGGCTG | 114792 |
| rs555420510 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118381 | CCCAGCACTTTGGGA[A/G]GCCGAGGCGGGCGGA | 114792 |
| rs555422903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019406 | GTGGACTCCACAGGG[A/G]ACACAGGAGCTAAAA | 114792 |
| rs555425738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119102 | GTCCTCTGGGAAACA[C/T]GCAGTGTTTGACAAA | 114792 |
| rs555431323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097732 | AAACTTTAAAAATCC[A/G]TCCTTATCACTGCCT | 114792 |
| rs555442573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926552 | GCTAGTGAATGGGGA[A/T]GCCCTTTCTGGATCC | 114792 |
| rs555459694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013374 | CTTGGTTTCGTTGTT[A/G]TAAAATGGAGAGAAT | 114792 |
| rs555462944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988871 | AAAAAACCAAACACC[A/G]CATGTTCTCACTCAC | 114792 |
| rs555475121 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021098 | AGTTGGCTCATACGA[C/T]TATGGAGGCTGACAA | 114792 |
| rs555493883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119635 | ACTACCTTGGCAAAA[A/G]GTTAGGATAAAGCCT | 114792 |
| rs555500744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127086 | TGTAGAGATTTGTCT[A/G]TGTGTACTATGTTCA | 114792 |
| rs555535832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076845 | AAATATTAAATAAAT[A/G]TATTAATATTTAATA | 114792 |
| rs555542341 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105060 | GCAAATCGCAACACC[G/T]GCTCACTTGCATTAG | 114792 |
| rs555551001 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109263 | AAATATAAACCCAAC[A/G]AGTAGGGATGACTTG | 114792 |
| rs555556364 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079107 | ATTCAAGAAGGTATA[A/G]TAGAATACAAGTGAG | 114792 |
| rs555563492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918499 | ACACATTACTACTGT[A/G]GGGTTAGAATTTTAG | 114792 |
| rs555570783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056251 | GCTGGGACTACAGGC[A/G]CCCGCCACCACGCCC | 114792 |
| rs555572389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028729 | TTGGCTGCCATATGC[A/G]AGAGATCAAACAGCC | 114792 |
| rs555576784 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948152 | CTCTGGAAAATCCCT[A/G]AAGTCTAGCTATTCC | 114792 |
| rs555594955 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984448 | CTTGTTAACTGTCTC[A/G]TTGATCTGTCTAATG | 114792 |
| rs555600375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015753 | ACCATGGGGAAAATG[C/T]CCCCAGGGCATGTCA | 114792 |
| rs555637059 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142192 | TTTTATTATTATATA[C/T]AATTTTATCATATGC | 114792 |
| rs555639244 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953456 | CCAACATGGCGAAAC[C/T]CTGTTTGTACTAAAA | 114792 |
| rs555641395 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920238 | CACAGACACCATCCT[C/G]TAACACTATGAGCAC | 114792 |
| rs555646295 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000958 | ATTCTATGAATCCAA[C/G]TATATGACATTCTGG | 114792 |
| rs555653296 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903120 | CAGAAAACAAACAAC[-/A]AAAAAAAAACAGTTG | 114792 |
| rs555661079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955275 | TTTGGATATATATTC[C/T]TTGATGCAAATTGAG | 114792 |
| rs555677546 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911339 | ACTCTCAGTCCTGCA[G/T]CCTGACCCATTCTAC | 114792 |
| rs555695397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041738 | TTCACATCCTCTTAA[C/T]TTTATGACTAAAGTT | 114792 |
| rs555714047 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056300 | TTAGTAGAGTCGGGG[-/T]TTCACCATGTTAGCC | 114792 |
| rs555725771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008902 | CTGGCTGTGCTTAGC[C/T]GGCCGTCTTGGCTCC | 114792 |
| rs555738329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912036 | TGCTTTATAGAGATG[G/T]CTTCCCAGAAGTCCT | 114792 |
| rs555743573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022546 | GCGATCTCAACTCAC[G/T]GCAATCTCCGTCTCC | 114792 |
| rs555777152 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938393 | AGGTGGTACTGGGGC[A/G]GGGCTGGGCCCCACA | 114792 |
| rs555779497 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056846 | GAGCTCGACACCAGG[C/T]TGGGCAACATAGCAA | 114792 |
| rs555786470 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928443 | GAGGATGCAACTGCG[A/G]ATGGGTGGGAGGGGA | 114792 |
| rs555792126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083422 | TGTACTTGGGGAATA[A/G]CAGAGATTCAGTGAC | 114792 |
| rs555792773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056687 | TCTAGACCAAGGATC[A/G]GCAAACTTTTTTTGT | 114792 |
| rs555793364 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986593 | CCCCTCCCCCAGCCT[A/G]GCTGCTGCCTTGCAG | 114792 |
| rs555803920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035344 | CTTTTATCTTTTAAA[C/T]GTTGGGGTAAAAGTA | 114792 |
| rs555823253 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982076 | TAGGCCCATTCAGTC[A/G]AGTGTTGAGTTCAGG | 114792 |
| rs555848801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940143 | CTAATCCATACAACT[A/G]TGTGATTATGGCAAT | 114792 |
| rs555856787 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963009 | CTTTTACACTGTTAA[A/G]TGAAAACCACTATGC | 114792 |
| rs555857613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050424 | GGCTTGAGAGAGCAT[A/G]GAGGTATGGCTGGCT | 114792 |
| rs555868124 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049572 | CGTAGAAAGCGAAAC[C/T]GTCGATAACGGGGGG | 114792 |
| rs555879195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905379 | TAACTCCAGAGCTAG[A/G]GTCTGTGTTTGTTCT | 114792 |
| rs555891812 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044055 | GGTCAAAATGGGCAT[A/G]CTTGTCTTGTTTCTG | 114792 |
| rs555891935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035748 | AGTCACTTTTCTTTT[A/G]CTTCTTTCAAAATTC | 114792 |
| rs555904182 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021222 | TGTGCAGGTTTATTA[C/T]GTGGGTAAATTGTGT | 114792 |
| rs555907562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036412 | CCTTTAGTGGTGTTA[C/T]GTTTCCCTGACATTT | 114792 |
| rs555916387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069469 | ACTTTCAATTCTGAG[A/G]AGCACTAGATTCTTG | 114792 |
| rs555932874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940765 | CTCTAAATGCTGTAT[A/G]GTCATTCATTTAGCA | 114792 |
| rs555936715 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027118 | AGTGAGCCGAGATTG[C/T]GCCACTGCACTCCAG | 114792 |
| rs555941110 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059224 | GTAGGATTTTGACAT[A/G]TGGAAATTAAAGGAA | 114792 |
| rs555946287 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037010 | AAAATGTTCAATTTT[A/T]AAAATTTATGATAAA | 114792 |
| rs555948099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021953 | GCATCCAGACTGCTG[A/G]CAGGTCCCCATAGCT | 114792 |
| rs555952807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941895 | AGGTGCAGGAAGTGG[C/T]TGTCCCATAACTTTT | 114792 |
| rs555980156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051680 | GACTGCACTCAGAAT[C/T]ATTTCCTAAAGAAAT | 114792 |
| rs555982318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136426 | GAGATACTCTTAGGT[C/T]GAGATTTGGACTTGT | 114792 |
| rs555983848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069946 | CAATGTATTATTATA[A/C]TTTTAATTATTAAAT | 114792 |
| rs555991281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942495 | AGTTGCCTTTTGTTG[C/T]TCTCTGGTTATCTTA | 114792 |
| rs556012816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958317 | GGTGCTATTGGATCA[C/T]ATAGGAGAGTAATTA | 114792 |
| rs556013344 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928133 | TGTTACAATGGAAAT[A/G]TAAGATTCCATAGAA | 114792 |
| rs556018815 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005996 | ATGCTCTTGTTTTGG[A/G]GCATCAAGTTCAGTA | 114792 |
| rs556020616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934652 | TATAACTAATTAGGC[A/G]GATTGCTGCAGAGAG | 114792 |
| rs556043806 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102135 | TTGGTTTTTCATAAA[C/T]GCACAAATATATTAG | 114792 |
| rs556045559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128565 | TTGCATCTTGCTCAG[A/G]ATCTCAATAACTCTA | 114792 |
| rs556069003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106700 | AGTGAGCTGAGATTG[C/T]GCCACTGCACTCCAC | 114792 |
| rs556078428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078459 | TTGATGAAACAAAGC[A/C]TTGTTAAAATAGCCA | 114792 |
| rs556082444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995949 | AGTGAAGTCCACCAA[A/G]CTACTGTTGAACACT | 114792 |
| rs556090610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030121 | ATAAAATGGGAGTCG[C/T]AGTGGTTTTGCCTGT | 114792 |
| rs556093717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057319 | CTCCTGTGTAGCTGG[A/G]ACTACAGGCACGCGC | 114792 |
| rs556100798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949671 | AGATCATATCTTCAG[A/G]GTTCCCTGGTGAGAT | 114792 |
| rs556113740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936740 | TATTTCTTTGCCTAA[A/G]ACTGCAGCAGCTTCC | 114792 |
| rs556122620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009039 | TCCTTGGGCAAGTGG[C/T]TTTATATCATTAAGT | 114792 |
| rs556125760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064793 | GTCATAAGCTGGCCC[C/T]CAACAACTGGAGCTG | 114792 |
| rs556130261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099547 | GCAACAGCTACTACC[A/T]TCTACTCATTCCTTC | 114792 |
| rs556146288 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939198 | TTCTGTGTTGTTATT[C/G]CTTCTTAAAGCTGCC | 114792 |
| rs556146451 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969984 | CCTGTTCTGGAAATA[C/T]CAAGTTGTATAAGCC | 114792 |
| rs556156069 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085676 | ATATGACAAAAAAAT[A/G]GATTGTAAAGTGATA | 114792 |
| rs556163675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972414 | GTATTACTATTGTAT[C/T]GATACAACACAATAC | 114792 |
| rs556163734 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964639 | GCCTGGGCGACAGAG[A/C]GAAACCCTGTCTCAA | 114792 |
| rs556177390 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088135 | CACTCTATATTTAGA[-/G]GTAACATAGAGAGTT | 114792 |
| rs556182962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065355 | CCCATTTTTATAGAT[C/T]TAAAACATCAGAGAC | 114792 |
| rs556192730 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122365 | GCATGGATTATGTAT[G/T]CTTCTATTCAAGATG | 114792 |
| rs556196088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002203 | GCTCAAAGACAGCCC[A/G]GCAGAGAGAAGGAAT | 114792 |
| rs556205050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079640 | ATTCCATAGCTAGTG[G/T]GGTATTGAGGACACA | 114792 |
| rs556212272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957365 | AACTTTTTATTACAG[A/G]ACTTTCTAATTAAAA | 114792 |
| rs556215144 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031341 | CATTAAGTTTTTAAC[A/G]TTTTTTTTTTTTGAG | 114792 |
| rs556224466 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958107 | GGAAACAAAAGAGAA[A/C]AAATGGGATGTGATT | 114792 |
| rs556237020 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995440 | TGGCTGTTCTTTTTC[A/C]AACCATTGTGCAGAT | 114792 |
| rs556249513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948954 | AGAAAACTTTCTTAT[A/C]TCCGACTTTAGAATC | 114792 |
| rs556265195 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092352 | GCTACTTTCTGGGTA[G/T]CTTCATAATATCTCC | 114792 |
| rs556291081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107468 | TGACTTGGGTTAAGT[C/T]GGTTAACTTGTCTGG | 114792 |
| rs556301707 | snp | C/G | 1.66479e-05 | 0.00288508 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967081 | GTCTGAACGCTGCCT[C/G]AGGTATGCCCTGTAG | 114792 |
| rs556303711 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913879 | TTCTTAAAGTCTATG[C/G]ATAGATTATATTACC | 114792 |
| rs556323835 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935797 | AAAGAAAGGAAAATC[C/T]CTGTTTTACATCAGG | 114792 |
| rs556326527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085020 | CCCTCCCATTTCTCC[A/C]ACCACTGTGATGAAA | 114792 |
| rs556326543 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974169 | CTCATGGTGTTGTTG[G/T]GCAGATTACATGAAC | 114792 |
| rs556326844 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093032 | TGACATATTTATGTT[A/C]TCTGCTTCTAATTTT | 114792 |
| rs556338609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959013 | AAGGGAGTGTTCTGG[C/T]AAAACAAGCAAATTA | 114792 |
| rs556344631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094208 | TTGAATAGCAATGAT[A/G]TTCATGCTAATTGGC | 114792 |
| rs556345583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129230 | TTTATTGTTGTTGTG[A/T]CTTGCTTCTTCCCTT | 114792 |
| rs556358481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974590 | ATCATCACCGTCTGT[C/G]AAGTTTTTTCTTTCC | 114792 |
| rs556366249 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941485 | TTTAATTCTTAAATA[A/C]GTTTTCTGAGTGACT | 114792 |
| rs556380366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079115 | AGGTATAGTAGAATA[C/G]AAGTGAGTCTGGGTG | 114792 |
| rs556389667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085653 | ATAAAAATTGTTTCT[C/T]AAACAAAATATGACA | 114792 |
| rs556417052 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030735 | ACTTGTGTTTCTCAA[A/T]TGTTTAGCTTACAGT | 114792 |
| rs556420166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985584 | TTCTTTTTATTCTTT[C/T]TTCTCTAAACTTCTC | 114792 |
| rs556423801 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108816 | AATGCTACCTCATCC[A/G]TAATATTAAGCTAAT | 114792 |
| rs556430742 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923211 | AATCCAATCAATATA[G/T]ATGGGCTTAAAATTT | 114792 |
| rs556432537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989772 | TCTTTACATAATCCA[A/G]TATTTCTTGGAGGAT | 114792 |
| rs556488804 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020011 | AGAGTGCAGCAATCT[C/T]GGCTCACTGCAACCT | 114792 |
| rs556494849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929484 | ATTGTTTTCCAATTT[A/G]TAGAGCAGAACTTAA | 114792 |
| rs556512073 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985849 | CAGAGTAGTTTGATT[G/T]TCTGAAGCCTTCTTG | 114792 |
| rs556513215 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011873 | GGCGTTTATTAAAAA[-/TCTT]TCTTTATTTGTTTGC | 114792 |
| rs556524196 | in-del | -/A | 0.265325 | 0.24953 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950232 | CTACATTTGTGTTAA[-/A]AAAAAAAAACCATTA | 114792 |
| rs556538416 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990919 | AGCAAGGGAAGTACC[A/C]CTGCAGTGGCAGTGG | 114792 |
| rs556544876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122068 | GATTATAAAGGGCAG[A/G]TGAATCTAATTGATA | 114792 |
| rs556550922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986140 | GTTGGAGGTCCACTC[C/T]AGACCCTGTTTGCCT | 114792 |
| rs556553403 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026749 | TGTTGAAATTGAGGG[C/T]TAAAATTTTAAGAGC | 114792 |
| rs556553426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004565 | GTTCCCGTTCTCAAG[A/G]GGAATGCTTCCAGCG | 114792 |
| rs556564787 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986562 | TTACCTACTCAAGCC[G/T]TGGCAATGGCGGGCG | 114792 |
| rs556580213 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041724 | TGTTAAAAATAAGAT[A/T]CACATCCTCTTAATT | 114792 |
| rs556590437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997574 | ACAGCATAGTGAGAC[C/T]CTGTCTCTATAAAAA | 114792 |
| rs556590968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108125 | CCATGTTTCCTAAGC[A/C]CTCTTTCGTAATGTC | 114792 |
| rs556605699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114650 | ATTAACATTCATTTA[C/T]TGAGCACCTACTCTA | 114792 |
| rs556607220 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922099 | TGACCTGGCACCCAA[C/T]TTCCTATAGTGAATA | 114792 |
| rs556620930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115655 | ACATTATAAACATGT[A/G]TTTTCAATCTTAGTT | 114792 |
| rs556650176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101332 | TTGCAGGATTACCTC[C/T]AACAATTCCAAATTT | 114792 |
| rs556651699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986787 | CCCCTTTCTTTGACT[A/G]GGAATGGGAATTCCC | 114792 |
| rs556681318 | in-del | -/ACTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065531 | ACTTTATAGAGTGTT[-/ACTA]ACTAATTTGCAATTT | 114792 |
| rs556684107 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937027 | TCATCTTACCCTGTA[-/T]TTTTTTCCCCACAGC | 114792 |
| rs556706527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131882 | ACCTTAGGCCCTCGA[C/T]TCTGGATCTGTGATT | 114792 |
| rs556737146 | snp | C/T | 9.89789e-05 | 0.00703418 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114275 | TGTCGCTATGACCCC[C/T]GCAGTAATTCCTGGG | 114792 |
| rs556738826 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081175 | GAAGGAGTGAGGGGG[A/G]AAAAGTGGACTAGAG | 114792 |
| rs556750317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045345 | TGTGAAGAAAGATAC[C/T]ATCTCTAAATTCTGT | 114792 |
| rs556767521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124232 | AAAGTTGCAGCACTA[G/T]GTTTGTTAGGCACCT | 114792 |
| rs556779633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011414 | CTAATAGTGATGACA[A/G]TTATTAATTACTAAT | 114792 |
| rs556789338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996776 | GCAACTATTCTAAAT[A/G]TTTTATGTGTATCAA | 114792 |
| rs556792602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012487 | CAGCCCTGCTGACAC[C/G]TTGATTTTAGCCCAG | 114792 |
| rs556800551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074501 | TCCAAAAGATAAAAA[A/G]CGAAAATAATGCAAA | 114792 |
| rs556807903 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047642 | TTCATGTTTCAGACC[A/G]GTCCTGAGTAGAAGA | 114792 |
| rs556809026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110318 | ACCTCTACCGTGTCT[A/G]CCTCCTTGGCACCTA | 114792 |
| rs556832323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138380 | CCCATCACTACAGAA[A/G]ATTTACAGATTAGCT | 114792 |
| rs556847133 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095201 | TAAGTGGCAAACACA[C/T]TTTAGGCTCTTTGGC | 114792 |
| rs556850208 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028800 | TGTATTCAATAAGAA[A/G]GCGTAAAAGTGCCAT | 114792 |
| rs556873373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915851 | AAAGCAGAAAACACA[C/G]AAAAAGCTCTTTGCC | 114792 |
| rs556877131 | snp | A/G | 1.67424e-05 | 0.00289326 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130761 | TCTTTTTTCAGAATA[A/G]GTGGATAAGCCGTAG | 114792 |
| rs556894647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018869 | ATCATAAGGAGAAAT[C/T]AACAAATTCTCAATC | 114792 |
| rs556913367 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006292 | TTAAATTGTTGTTGT[A/T]GATTTATAGTCTTTT | 114792 |
| rs556916956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976400 | AGACCTCCCTTGGCA[C/T]CTGAGCCAAGGAGTG | 114792 |
| rs556928918 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997908 | TATGTAAATGGAATC[-/A]AATGTTGGATTCATG | 114792 |
| rs556940452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123369 | GTGGCGAGTTGTACA[A/G]GGAAGCTTAAGAAAA | 114792 |
| rs556960130 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910297 | AAGCAAAAAAAAAAA[A/T]TTAGACAAAATTTAC | 114792 |
| rs556968681 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140709 | TTATTCATGTAACCT[C/T]TTTTTGTAATCAAAA | 114792 |
| rs557010352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025681 | TTCCAACTTGAGAGG[A/G]AGGCACCTGAGTAGG | 114792 |
| rs557016265 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039968 | ATTAAAAATTAAGAC[A/T]ATATTAAATTATCAT | 114792 |
| rs557031017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982452 | GGGGTCATTGCATGT[A/G]AGATGGGTCTCTTGA | 114792 |
| rs557090081 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031360 | TTTTTTTTTGAGATA[A/G]AGTCTCACTCTTTTG | 114792 |
| rs557103722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931415 | TAGCAGCCTACCACA[C/T]AGGAAGTTAGCCTGA | 114792 |
| rs557114050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066191 | CTTGGGCTTTACGCA[A/T]CATCACCTGATTCAC | 114792 |
| rs557129878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902050 | TGAACATACATGTGC[A/C]TATGTCTTTTTATTA | 114792 |
| rs557135940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034421 | TTACTGTAGCTTTGT[A/C]ATATATTTTGAAATC | 114792 |
| rs557141026 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999328 | TTGAGCCTGGGAAGT[C/T]GAGGCTGCAGTGAGG | 114792 |
| rs557175638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066947 | GTGCCCCTTCAATCA[A/C]TGCTGATATATTCTC | 114792 |
| rs557187000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939609 | AGAGTGTTTCAAGTA[A/G]TGGGAAAAAATTCTA | 114792 |
| rs557196714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016250 | TGCACTGTGTGCCTC[A/G]GAAAGCTGAAGACAT | 114792 |
| rs557199134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073182 | TTTCTGGAAATGTCA[A/G]CAAATTTTCTGCCTA | 114792 |
| rs557202731 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945471 | GCCCAGTGGGCCAGC[A/G]TCAGAGCAAAAGTTT | 114792 |
| rs557204100 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038341 | AAAAAAAAAAAATCC[A/G]ATTTAAAAATGGGCA | 114792 |
| rs557242706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060529 | TCATCATGCTCTATA[C/T]AGAATCTCACCTCAG | 114792 |
| rs557248111 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996775 | GGCAACTATTCTAAA[A/T]GTTTTATGTGTATCA | 114792 |
| rs557260849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028471 | AAGAATCCCCCTCTC[C/T]GTCTCCTCAGTTGCT | 114792 |
| rs557269346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968270 | TGTTTTTGGATGTCA[C/T]GGGGATTGTGGATAC | 114792 |
| rs557272571 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925567 | AAGATGACTGCAGTT[A/T]AGATCCCTTCTTCCC | 114792 |
| rs557329701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075853 | TTTCTAAAGCCGTAT[A/T]CACTTTTTTGTCTTA | 114792 |
| rs557355251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968588 | TTAAGTCTGCCATCC[C/T]GTTCTTATTAATCAA | 114792 |
| rs557379169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062265 | GTTGTGTGAAATGAG[C/T]GCAACTGACAGGATT | 114792 |
| rs557382355 | in-del | -/AATCC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124519 | TAATAGCTACATTCT[-/AATCC]AATCCATTGGTTGTA | 114792 |
| rs557390729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068644 | GCTGCTGTGGTCATT[C/T]ATCAGCACACTTTGT | 114792 |
| rs557429796 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000078 | ATGGGACAAAGAAGG[A/C]AAAGTCAAAGATAAA | 114792 |
| rs557441642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926601 | AAAAAGTTGTGTGTG[C/T]GTTTCAGATGTGTGC | 114792 |
| rs557444927 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990540 | GCTGCAGATCTTGGA[C/T]TGGCACTCCCAGGGT | 114792 |
| rs557446872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089502 | GTCCTTTTCTGGGTA[A/G]GCGCGGTGGCTTACG | 114792 |
| rs557489233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041460 | TTGCTGTCAAAGTCT[C/T]ATAACTGTCTTTCTC | 114792 |
| rs557502456 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056400 | GTGAGCCACCAGGCC[A/C]GGCCCACCAGCCTGC | 114792 |
| rs557507297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969836 | AGACTCCTTTCTGAG[C/T]TCCAGATCCAGGAAT | 114792 |
| rs557508170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082021 | AAAGCAAATAACTTA[C/T]CAGACTTATCAGTGG | 114792 |
| rs557519808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993204 | CATAACAAAGTACCC[A/G]AAAACCTAGAGGCTG | 114792 |
| rs557531252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964373 | AAAAACAAATATATG[A/G]TCGGGCGCAGTGGCT | 114792 |
| rs557547073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946357 | TATCTCGTGGCACAC[C/T]ATATCACTTACTTAT | 114792 |
| rs557569035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082395 | GAGGCGGGCGGATCA[C/T]GAGGTGAGGAAATCA | 114792 |
| rs557590142 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946139 | TCAACAGGATTAGTA[A/G]GCTTTTAGATATTCA | 114792 |
| rs557600755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097812 | ACGACAGGGATACTT[C/T]AGCCAGTTTGCTAAT | 114792 |
| rs557621412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126970 | AATATCAAGAGATAT[C/G]AAGATATCACTGTGT | 114792 |
| rs557640415 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968082 | GACCAGCTTCTTTCC[A/G]TGACTCTGAAGCTAT | 114792 |
| rs557643336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049581 | CGAAACCGTCGATAA[C/T]GGGGGGCGGGGGGGA | 114792 |
| rs557643589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000985 | CTGGAAAAGGCAAAA[C/T]TATGGAGACAATAAA | 114792 |
| rs557648954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083758 | TTATAACTAGAAATG[A/G]CACTCTTTCTATAAC | 114792 |
| rs557656117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076662 | TTAGGTGTACTTATA[A/G]TATTTCTAAATCATG | 114792 |
| rs557659821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090830 | GAGCTATGTCTACTT[G/T]GGTCTATAGCTTCTA | 114792 |
| rs557678065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034107 | TTATTGCTTAGACCA[A/G]TGTCAAGGAGCTTTT | 114792 |
| rs557692507 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912769 | ATCCAGGACTCCTTG[C/T]CTGACTTGGAAAATC | 114792 |
| rs557699862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983962 | CTCTAGTTCTTTTAA[C/T]GGTGATGTTAGGGTG | 114792 |
| rs557704727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042401 | TGTGGTCAGGTGTGG[C/T]TATCAGTACACAATT | 114792 |
| rs557708626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077607 | CAATTGTATGAAAAA[C/T]CCAGTACCTAGATAG | 114792 |
| rs557716263 | in-del | -/CA | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976357 | CCTCTCTGGGCAGGG[-/CA]CACCTGGATGTCCCT | 114792 |
| rs557733962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994154 | CAAGAAACTCATGGA[G/T]AATTGTCTCCCAACA | 114792 |
| rs557748775 | snp | A/T | 0.000121544 | 0.00779468 | intron-variant, splice-acceptor-variant | KLHL32 | GRCh38.p7 | 6:97105441 | TTTTTCTGAATTTGC[A/T]GAAGTGTGGAATTTG | 114792 |
| rs557771721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078293 | TAAGAACTTCATGTA[C/T]GCTACTACATCATGG | 114792 |
| rs557788811 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014830 | GCCTCCTACTCTGCT[C/G]AATAGCTTAGTATGA | 114792 |
| rs557811380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970712 | ATTCATAATTAAGTT[A/C]CTTTCTACAGAGTTT | 114792 |
| rs557819153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927248 | AAGTGGAGAAAAACT[C/T]AGTTGAGTGCTTGTT | 114792 |
| rs557824019 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127816 | GTATTAACTTAATAT[A/T]GCCCAAATGACCTAA | 114792 |
| rs557892289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980192 | TGGCTAGGACTTCCA[A/G]TACTATGTTGAATAG | 114792 |
| rs557893354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989160 | TTGTTAGCTGGTTAT[C/T]ATGCAGACTTGATTG | 114792 |
| rs557909395 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115458 | TCTCTTTTGAAAACC[-/T]TTTGATTATGGAAAA | 114792 |
| rs557920731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105778 | GACAAAAAAAAAATA[C/T]TTGTTACTTTTAGAC | 114792 |
| rs557925415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007582 | TGAGTTGCCACAGTT[C/T]TTGCACTGGTTCTTT | 114792 |
| rs557928164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098759 | TTCCTCACTGCAGTA[C/T]ACCACAAATGATTAT | 114792 |
| rs557941444 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029500 | TTACTGTTTTAGTTT[G/T]TCTTGTGATATTTTA | 114792 |
| rs557949181 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048720 | CATCAGGCCAGGCAG[C/T]AGAGTGACAGGAATC | 114792 |
| rs557957931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022032 | CTGGTCTAAACTACC[A/G]TTATGTTTTGCCTGG | 114792 |
| rs557984987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008992 | AGTCTAATTTATAAC[A/G]TCTCTGTTCACATAC | 114792 |
| rs557994749 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979300 | AAGTCTTTAATCCCT[C/G]TTGAGTTGATTTTTG | 114792 |
| rs557999376 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107229 | ATCCAGGAGGCGGAG[A/C]TTGCAGTGAGCCGAG | 114792 |
| rs558032966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994698 | TTCCTGTGATCATCA[C/G]CATTTTAAAAGAAAG | 114792 |
| rs558068497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009487 | TCTGTTTTAATTTGC[A/T]ATAGAGCACTTGTAT | 114792 |
| rs558072719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002405 | AATTTAAAAATATAA[C/T]GAATATAGCTTAAGA | 114792 |
| rs558078264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135469 | TGCCACCATGCCCAG[C/T]TAATTTTTTGTATTT | 114792 |
| rs558079193 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980712 | TCTTCCTTAGTTTGT[-/A]AAAAGTAGTTTTAGT | 114792 |
| rs558087122 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905687 | GTAAACATTCAAAAA[A/C]TATTAGCTATTATTC | 114792 |
| rs558095986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064570 | ATATCTACATATTAA[A/G]CAGCATTATATTTTT | 114792 |
| rs558105688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002967 | ACTGAACATGCATGT[A/G]TCTTTATGGTAGAAA | 114792 |
| rs558118353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016576 | ACAGGCTTATAGGTG[G/T]AAGGGACTTTCCTTG | 114792 |
| rs558120980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988923 | AACACATGGAGACAG[C/G]AAGGGGAACATCACA | 114792 |
| rs558138006 | snp | C/T | | | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062396 | GAGCTGCACTAATTT[C/T]GTGAATGTCAGTCAA | 114792 |
| rs558140509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099612 | CTGAGACTATCAGGC[A/G]GCTGGTTCTCCACCA | 114792 |
| rs558153039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973628 | CATGTATATTATTCT[A/G]AAAGGCTGATTTTGA | 114792 |
| rs558153301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128309 | CATTTCTCTCTTTGC[A/G]AAGTGTGTTTCCTGA | 114792 |
| rs558162723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137407 | AATAAAGAGATTGGG[A/G]CATCTAATCTCCACT | 114792 |
| rs558193523 | in-del | -/TTTTT/TTTTTT | 0.277334 | 0.248501 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973730 | TCTTTACAGATTGCC[-/TTTTT/TTTTTT]TTTTTTTTTTTAGAC | 114792 |
| rs558209145 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118389 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCGCCTGA | 114792 |
| rs558218948 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120710 | GCCCCCTTGTTGTCC[C/G]TGGAGGCGGCCATGA | 114792 |
| rs558224264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138147 | TTTGACAAATGGGGC[A/G]AGAGCAGCTCTCCTG | 114792 |
| rs558227491 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918266 | AAATACCTTTGAGAG[A/C]ACTTGAAATAAAATT | 114792 |
| rs558228641 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914002 | CAACGTAATGAGAAC[C/T]GTCCTTAAAAGTGGA | 114792 |
| rs558232672 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129535 | TTCCCATTACTGAGG[G/T]TGAACAGGAACCAAA | 114792 |
| rs558235030 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053465 | TACTGCAAATTCTAT[A/G]AAAAGAAATTACTTT | 114792 |
| rs558235304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070871 | GGAAATTGGTGGGGG[G/T]TGTGTAAAAGAAGAT | 114792 |
| rs558237949 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934682 | GCAGCTAATATCCTC[A/C]TAGTTGTCCATATGG | 114792 |
| rs558242960 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050298 | CCAAAATCTGATTTG[A/G]ATGTTGAGACTGATA | 114792 |
| rs558257691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022740 | CTCCCAAAGTGCTGG[A/G]ATTATAGGCATGAGC | 114792 |
| rs558262843 | snp | C/T | 8.23662e-05 | 0.00641688 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897801 | TCACTAGTGCTCCCA[C/T]CTCCTCATAACATTA | 114792 |
| rs558263831 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031036 | AAGATGTTATATGCT[C/T]AAAAATATTACTGCT | 114792 |
| rs558274385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029968 | TACTGTAATCATTGC[A/G]AGTTGCTCTTTTCAA | 114792 |
| rs558289599 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129824 | GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCAT | 114792 |
| rs558293250 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069384 | GAGTTAAGGAGAATT[C/G]TGGGTGATTTTGTTC | 114792 |
| rs558293698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030848 | GAATTCTTTTTGTTT[A/G]TGACACTGTAGGGTG | 114792 |
| rs558296457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063891 | TTTTGTCAACATGGT[C/T]GTGTGCCTTTTTTCC | 114792 |
| rs558325505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935191 | ACTAGCTGAGAGAAA[C/G]GCAGACATCATACTT | 114792 |
| rs558328543 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093804 | GTACACGATGGTGTA[C/G]TATAAAGCAGGAAAT | 114792 |
| rs558330453 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031414 | GATCATGGCTCACTG[A/C]AGCCTCAAACTCATG | 114792 |
| rs558340976 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042420 | CAGTACACAATTTTA[C/T]AGATAGGGTGGTATT | 114792 |
| rs558369581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045132 | AGAAGAAAATAGTAA[A/G]TATAAAGGAAATAAG | 114792 |
| rs558390422 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009203 | GTATTGGTGATGGTA[A/T]CTAGTTTTCAAGCAC | 114792 |
| rs558413046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921327 | GGCAGAGAAAATGTA[A/C]ACATGAAATAGTTTA | 114792 |
| rs558414480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965350 | ATTTTAGAAAACACC[C/T]GATTTAGTGAGTTGG | 114792 |
| rs558457620 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011177 | TCTAGCCAAGTTCAC[A/G]TTAAATTCTACTAGG | 114792 |
| rs558462773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100235 | TCATAGTTCCCTAGT[A/T]TTTTATACTATGATG | 114792 |
| rs558474225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913570 | TAACTTTTTGCAAGC[A/G]GTGCAAGCAGGCTCC | 114792 |
| rs558478056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051106 | TGAGGAACCCACTGT[C/G]GGCTAAGGTGCCTGA | 114792 |
| rs558502794 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027017 | AAATACAAAAACCAG[C/G]TGGGCGTGGTGGCGT | 114792 |
| rs558521012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093157 | CCCTGCAGTAATATT[A/G]CTGCTAACCTGGGTT | 114792 |
| rs558555648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123080 | CATAGACATCTACTC[C/T]TGGAGTTTACTCTAT | 114792 |
| rs558556478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059798 | CATTTTATGTGTGTT[A/G]AATATATGATCATTT | 114792 |
| rs558571992 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904170 | AACATACTAAAACCC[A/C]GTCTCTACTATAAAT | 114792 |
| rs558589968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958380 | CAGAGGAGGTGACAT[C/G]TGAAACCTGCAGGAT | 114792 |
| rs558592370 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019515 | AGGTGTGGGACTTCG[A/G]GTGAAGCACTCACAG | 114792 |
| rs558596434 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037071 | ATGTTAGCTTTTTAA[C/T]ATATCAAATATAATT | 114792 |
| rs558616601 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053120 | CACACACATTCTCTC[A/C]TGACCTCATATTGTT | 114792 |
| rs558627826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115367 | TGGTAGTTACTTGTG[C/T]CATTCTAACCCTTCA | 114792 |
| rs558632515 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907300 | TCTATATACTTTCCC[A/G]TTTTCTACCTCACTA | 114792 |
| rs558640368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085973 | GAAGTTGATTATTCA[A/G]TTAAATCCTCTTCTG | 114792 |
| rs558643224 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974868 | TACAGGAATTACCAA[C/G]ATGGGAGAGACACAG | 114792 |
| rs558703696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079206 | TTTGGTCATTTATTA[C/G]TAGTTCCTGCATAAT | 114792 |
| rs558714111 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950512 | CGTTAAAAAAAAAAA[A/C]CCCAGACACTTTGCT | 114792 |
| rs558715351 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071673 | CATCATCTTTCTAGT[C/T]ACTCAAACCTTGGCA | 114792 |
| rs558728335 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001155 | ATACAACACCAGGAG[A/T]GAACCCTAACGTAAA | 114792 |
| rs558729251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975534 | TTGTGTCCTGTGGGA[A/G]ACATGGTAAGGTACA | 114792 |
| rs558735851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960308 | TTACTGAACAATTCT[C/T]GTTTACCGTACTTTT | 114792 |
| rs558737432 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011497 | TTGTGCCTTTTTGCA[G/T]AATGAATGAGAAAAG | 114792 |
| rs558759735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072629 | TCATTATGAACTTTG[C/T]GCATTTCCCTGTACC | 114792 |
| rs558763335 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079697 | ACTTGTCATTCACAC[A/T]ATGAGAAACAAATAG | 114792 |
| rs558777221 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001537 | CAGTGGCACAATCAT[G/T]GCTCACCAAAGCCTC | 114792 |
| rs558819770 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065408 | GAGGCAATATGGCTG[A/G]TAGGACGTTCTGATT | 114792 |
| rs558820644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952296 | TGTTTAATATTAGAA[A/G]TGTTTTGGGCATTTT | 114792 |
| rs558822488 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986190 | TGCAGAACAGCAGAT[A/T]TTGGTGAACAGCAGA | 114792 |
| rs558827149 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073927 | CTACCAACCTTTTTC[C/T]TGCTGCACATCAAGG | 114792 |
| rs558832162 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955512 | GAAAGATGAAAAAAA[-/T]ATTTTAAATTAATGT | 114792 |
| rs558841438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908441 | AAATGTCACATGAAT[A/G]TTATTAACAGGGTTC | 114792 |
| rs558846288 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002787 | AGCTCCATCCATGTT[C/T]CTGCAAAGGACATGA | 114792 |
| rs558849004 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931595 | TTCAATATTTCTAAA[C/G]ATATAGTGCAATTTC | 114792 |
| rs558873877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974779 | CCTGCCAAATAAACC[C/T]ACCATGCAAACTAGG | 114792 |
| rs558886953 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940070 | TACAACTGCAAGTGC[A/G]AAGGTAACATTCCAT | 114792 |
| rs558897407 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075962 | TGTAGATTTGCACAG[C/T]GGGGTCTTGATAATC | 114792 |
| rs558899120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047018 | TTGTTGCTGTCTTGG[A/G]GAGAAATTGGAAGTA | 114792 |
| rs558909462 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119700 | CTAAACTTCATTCCC[C/T]GAATCTGAGCTTATC | 114792 |
| rs558910085 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981967 | GGATTGTTTTATGGC[C/T]AATTGAGTCATCAAT | 114792 |
| rs558912581 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981440 | TTATTTGGATTTTCT[G/T]TCTTTCTTTTATTAG | 114792 |
| rs558915521 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139849 | CAGTTGTTGAAATAC[C/T]CAGATTTTTCACCTT | 114792 |
| rs558916998 | in-del | -/AT | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915681 | GGATGGATAATACTC[-/AT]AGAATTTTATTAAGA | 114792 |
| rs558938536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109331 | AGTTATATGAAATCT[A/G]TGAGAAGTTAGAAAT | 114792 |
| rs558938757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088385 | CACTTGCCTTTGTGA[C/T]CTGGCAAATCTCTAT | 114792 |
| rs558961573 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040012 | ATATGTACATTCCTT[A/G]GGCATTGATAAAATT | 114792 |
| rs558992032 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016579 | GGCTTATAGGTGGAA[A/G]GGACTTTCCTTGTCT | 114792 |
| rs558999088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938686 | GGATTTGGAAATAGA[C/T]GGGCCTAAGCTTGAA | 114792 |
| rs559000006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102729 | AATGGGTTTCATTTT[C/T]CCTATGGCATCATTG | 114792 |
| rs559010677 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056348 | CTGACCTCGTGATCC[G/T]CCCGCCTTGGCCTCC | 114792 |
| rs559038934 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115720 | TTTTTCTATCAGGAA[G/T]AAAGCTGCATTTTCT | 114792 |
| rs559059357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046273 | CTTGAAAGATGACAG[A/G]CCCAGGGAAATGCAG | 114792 |
| rs559062477 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066251 | GCATGCTGACACAGT[G/T]TGGTTAGAGCGTTAG | 114792 |
| rs559068355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005030 | TACATCCTCCCCAAT[A/G]TTTTTGAATAGTTTT | 114792 |
| rs559076626 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037061 | TACATTATGAATGTT[A/G]GCTTTTTAATATATC | 114792 |
| rs559096426 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087722 | GCAGGTGGCTCTTCT[A/C]CTATGTACTGATAAT | 114792 |
| rs559103021 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989833 | AATTAGTTCAGAAAC[C/T]AGCCTTCAAGCTCTG | 114792 |
| rs559125034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909113 | CTGACTTCTGCTGCT[A/G]GATTTTTTTCTACTC | 114792 |
| rs559127442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060220 | AAGATGCCAACTCAC[C/T]TGATCACAGGCAGGA | 114792 |
| rs559164013 | snp | A/G | 6.59076e-05 | 0.00574016 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139219 | CTTCCTTCCAGCTCC[A/G]TATTTTACATGCCCT | 114792 |
| rs559176237 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005492 | CATTCGATTCAGCTC[C/T]GATTTTGGTTATTTC | 114792 |
| rs559193355 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948298 | TTATTTCACCTTGTA[C/T]GTCAAACTTGAGGTT | 114792 |
| rs559197199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943651 | GTCTTGTCTTTACTG[A/G]TTGCTCTTCTTTGGC | 114792 |
| rs559199582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900213 | AAAATTGGGATAATA[G/T]TAATCACCTAAGGGG | 114792 |
| rs559206428 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902377 | CTTTTTTTCATGTTT[C/G]TTGGCTGCATGTATG | 114792 |
| rs559218856 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899863 | GGATGCTGCTTAGAA[C/T]GAAGCTTCCATCTGA | 114792 |
| rs559261996 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998443 | AAAGAATTAATAAAA[A/G]TAATAGTAAAATAAC | 114792 |
| rs559263372 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901116 | GAATGATCAACCAGC[A/C]ATTATGCCCAGATGC | 114792 |
| rs559283353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095945 | CTTGAAGTCCATTTA[C/T]ATGTAGGTAGAACGA | 114792 |
| rs559295071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975120 | TGTTTATGGCATTAC[G/T]TCTGTATTATTGTAG | 114792 |
| rs559329015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900480 | TATTTGCTGATTAAC[A/G]TGCTCAGCACACGTG | 114792 |
| rs559329031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033093 | TACTAAGAGCTTGCC[A/C]TATGTCAGGCACTGT | 114792 |
| rs559357737 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141616 | TTTAAGTGAACTACA[C/G]TATAGTAATTCATCT | 114792 |
| rs559358213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975396 | TTGATGTTCTTATGG[C/T]GCACAATTTCCGAAG | 114792 |
| rs559394794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991981 | GGGCAGCAAGAGCGA[C/G]GGCTTCCGAGCGGCA | 114792 |
| rs559404142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060584 | GGATTCTGGCCCCAT[A/G]TTCTGCCTGGAGACC | 114792 |
| rs559418747 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106326 | GATTATATATCATAT[A/G]TTCTACTCTGTAGAG | 114792 |
| rs559443001 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995670 | TTTGCTAGTGACCAT[C/T]CTTTCCACCTGTAAC | 114792 |
| rs559446717 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012583 | AAGTTTGTGGTACTA[C/T]CACAGTAGCAAGGAA | 114792 |
| rs559459945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033366 | GATTTTCTTCTTTTT[A/T]AAGGCTAAATAATGT | 114792 |
| rs559465494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916688 | TGTATGTCTTTTCTT[C/T]TGTTAATCTGTATTT | 114792 |
| rs559470861 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014291 | CAGAGCGAGACTCCG[C/T]CTCAAAAAAAAAAAA | 114792 |
| rs559495617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053391 | CTTGCTCCATAAATA[A/G]ATCATTCCACACATT | 114792 |
| rs559504833 | in-del | -/TGTA | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139462 | CGTCACCCTTCTCAG[-/TGTA]TGTATGTCAACATTC | 114792 |
| rs559540293 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951832 | AAGTATAGAAGAGGC[A/G]ACTGCTTTCAATTAT | 114792 |
| rs559542243 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932660 | CAGACTTAATCTCCC[A/G]GGCTCAAGCAATCCT | 114792 |
| rs559545487 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020167 | AGGCTGGTCTCAAAC[C/T]CCTGACCTCATGATC | 114792 |
| rs559581585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117944 | GCATTTACTCAAAAG[C/T]AATATTTAGTGCTTT | 114792 |
| rs559592027 | in-del | -/TCTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983340 | ATTGGTCTAAAATTC[-/TCTT]TTTTTGTTGTGTCTC | 114792 |
| rs559603201 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140801 | AAACATTGAAAATAC[A/T]TAAAACATTGAATAT | 114792 |
| rs559607763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068227 | GCCCAAGCATATTAT[A/G]TTGTTTTATTAACAA | 114792 |
| rs559610776 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926637 | TCTGACAAGTGAGAT[A/G]AAGGAGTGGAGCAGG | 114792 |
| rs559621855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918925 | AAAATGAAGAGCCAT[C/G]TCTCCGCCTGTGCAG | 114792 |
| rs559623576 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114873 | TCACCCCTGGCTACC[C/T]GACTAGAGCCATTTC | 114792 |
| rs559672284 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952820 | GTTGGTCTTTTGAGA[A/T]GTTTTTCAGACCTTT | 114792 |
| rs559679786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992449 | GAAGAGCTAATGTTT[A/T]CTCACTACTCTCTTC | 114792 |
| rs559706423 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033856 | TCAGATCCTGTGACC[A/C]TTTTAAAATTCAGTT | 114792 |
| rs559753538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006731 | TCTGAAAAGGATCTT[A/C]TTTCTCCTTTGCTTA | 114792 |
| rs559758243 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010573 | AAGAATTTATCCCTC[A/G]TGTTTCCTCAATTTT | 114792 |
| rs559771068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082168 | TAAGGAACAGAACAA[G/T]AAATACTAAAGAGGA | 114792 |
| rs559772879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074882 | AATATATATATATAT[G/T]AATTTCTTATATATA | 114792 |
| rs559802300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955500 | ATTTCCTCAAGAGAA[A/G]GATGAAAAAAATATT | 114792 |
| rs559802656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947142 | AGTAAAATGAAACAA[A/G]CATAACCAGCTGAAA | 114792 |
| rs559816297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961818 | GATAATGGAGTTTTT[A/G]GCTCTCTGATATCAA | 114792 |
| rs559837638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075565 | TAACTTCTTTCCTAT[A/G]TAACTGATCCCAAGG | 114792 |
| rs559854306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983142 | ATTGAGATAATCATG[C/T]GGTTTTTGTCATTGG | 114792 |
| rs559871115 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142398 | TACACCTTATTAAAT[G/T]TGTAAAGAATATGCT | 114792 |
| rs559873852 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063978 | AAGTGAAAAATTGGT[A/G]TCACCAGGATACTTG | 114792 |
| rs559890285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947755 | CTTATAAACATGCTG[G/T]GAGGTAAGTAGTATT | 114792 |
| rs559900933 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980572 | ATTTGCTAGTATTTT[A/G]TTGTGGATTTTTACA | 114792 |
| rs559910255 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111327 | TCACCCTTCTGATGT[A/G]TCCTAGGCAGGCTCC | 114792 |
| rs559912263 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954468 | TTACCCCATAAAGTG[A/T]TCTGGTTGAGCCATT | 114792 |
| rs559913003 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077181 | GAGTGGCCTGCCTTT[C/T]CCTGGAGATGGAATC | 114792 |
| rs559924834 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079945 | TTCAAAACCACTACC[A/G]CTACCTGGATACTTA | 114792 |
| rs559929797 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125677 | GTTTGGTGCAAATTG[A/G/T]TGTCTATCACAGTTA | 114792 |
| rs559938758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061796 | TAAATTCACCACACT[A/G]TAAATCATGAGGAGA | 114792 |
| rs559957431 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014226 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 114792 |
| rs559962603 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956214 | CCTCTCACTGGGTCC[G/T]TCCCACAACACTTGG | 114792 |
| rs559966570 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082544 | CATGAACCCGGGAGG[C/T]GGAGCTTGCACTGAG | 114792 |
| rs559966644 | in-del | -/AA | 0.0457969 | 0.144226 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950501 | ATCAGTTGTCACGTT[-/AA]AAAAAAAAAACCCAG | 114792 |
| rs559974897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034919 | CTTCAGGGTTTCCTA[C/T]GTATATAATCATGTT | 114792 |
| rs559976406 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077633 | GATAGCATCGCAAGG[A/G]ACTTTCTGAAGCTCA | 114792 |
| rs559983194 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920571 | AAAACACACACAATT[-/AC]ACACACACACACACA | 114792 |
| rs559983352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977267 | AATAACAAAGACTAA[A/G]TAATTTGCACTAACT | 114792 |
| rs559987114 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054410 | CTAGTTGTTAGGGAT[A/G]CACTGATGAGAAAAT | 114792 |
| rs560031080 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903317 | CCCTTGTGTGACATG[C/G]TTCTAGCCAATAGAA | 114792 |
| rs560033929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978736 | CGGCTTTCCACAATG[A/T]CTGAACTAATTTGCA | 114792 |
| rs560038084 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070378 | TAATCCAGAATATCA[C/T]ATTTGCCAAATAACA | 114792 |
| rs560039563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007169 | CATTATCCCATATTT[A/C]TTGGAGGTTTTGCTC | 114792 |
| rs560050746 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923049 | GAGATACCCTGAGAC[A/T]CTCAGCTTGGGCAGT | 114792 |
| rs560052009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962551 | GTATTAAAAACACTA[A/G]TATTTGGCATATGAA | 114792 |
| rs560061747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911547 | CTCTACCTTCTACCC[C/T]GAATCTCTTCCCCTG | 114792 |
| rs560072468 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140343 | TGACATAAATTTGAA[C/T]CTAGAATTGGCAGTT | 114792 |
| rs560088502 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966088 | AATCATCAGAAATAG[A/G]CACAGCTTAACATAT | 114792 |
| rs560119023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119269 | ACTGCTACTCTCTCA[C/G]CCCTTTCCTTCACTG | 114792 |
| rs560125408 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945595 | TTTAAAAAGGGTAGG[-/A]AAAAAAATTTTAAGC | 114792 |
| rs560128129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097349 | TAGAGGCTGCTGTGA[C/T]AATGAAAGGTTGATT | 114792 |
| rs560156496 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971853 | AAAGGGTAAAAAAAA[A/T]TTTTTTTTCTGTTGT | 114792 |
| rs560172858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000452 | TTGTGTGCTGGTAAC[C/T]GGATTTCTGATCTTG | 114792 |
| rs560179749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111851 | GAAGGTAATCTTCCC[C/G]TGAAGTCTGGCCATC | 114792 |
| rs560184418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042469 | TGGGAGCTCATTTTT[C/T]TACTGAATTTTATTT | 114792 |
| rs560191142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941676 | ATAAGTGAGCCTGAG[A/G]AAGTATCCTCTCAGG | 114792 |
| rs560191487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099199 | TGACATGACTGCCAC[C/T]GTCCTGCTCTCAAGC | 114792 |
| rs560192582 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128624 | CTAGGCCTTTGTGGA[A/G]AGTCGATAATGCCTG | 114792 |
| rs560206533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985058 | AGGAGCTCTTGTAGG[A/G]CAGGCCTGGTGGTGA | 114792 |
| rs560219585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015241 | CAGTACAGGAAATTG[A/G]TACTGCAGAGAGTAG | 114792 |
| rs560223344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934717 | TCGGTTGATTAATAA[C/T]ATACATTTCTGCATA | 114792 |
| rs560228272 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134182 | GAACCAAAAAGTAAT[A/C]TCAAAGAAAGTAGAA | 114792 |
| rs560237370 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905120 | ATAGCAATTTAATCA[A/G]TACAACAGTTGTCCA | 114792 |
| rs560254267 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099698 | CTCTGGGCCACTTCT[C/G]CCACCCGAACTAAGC | 114792 |
| rs560260090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001106 | CTGTAATGGTAGATA[C/T]AAATAATCATACATT | 114792 |
| rs560289930 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988654 | AAAGATACATGCACA[C/T]GTATGTTTATTGCAG | 114792 |
| rs560295865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995181 | ATAGTACCTGACACT[C/T]AATAAATGTGAGCTG | 114792 |
| rs560315133 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913035 | TTCAATGTTTGATTG[C/T]TCTCTGTTTCTGCTA | 114792 |
| rs560320208 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020078 | CTGCCAAGTAACTGG[G/T]ATTATAGGTGCCAGC | 114792 |
| rs560324156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092618 | GTTTTATCCTTTGAG[A/G]GGCCCCTAGCTGGAC | 114792 |
| rs560353744 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127287 | TGGGCTCACCATGAG[A/G]GTATACAAACAGATC | 114792 |
| rs560379380 | in-del | -/TTTGGTTACTGTAC | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902997 | TTACTGTAGCCCTGT[-/TTTGGTTACTGTAC]AGAATAGTTTGAAGT | 114792 |
| rs560382160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000376 | TTGTTACACACTGTG[A/T]CAGTTCAATGGGCAT | 114792 |
| rs560384604 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937053 | CAGCTCTTATCGATT[-/A]AAAAAAAAAAAGTTT | 114792 |
| rs560385925 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995631 | ACACATTCTTTCCAC[C/G]TCAGGGCCTTTGCAC | 114792 |
| rs560386527 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909500 | TACTGCTACTCTGTT[C/T]GCACTGTTGTGGGTT | 114792 |
| rs560393674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934416 | GCCAGGCCATCTGGA[C/T]CTGGGCCTCAGCTTT | 114792 |
| rs560396884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028895 | TAGGAATGTATTGTG[A/T]TCCCACGTTCAGGGG | 114792 |
| rs560428057 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091997 | TTTTTTTTTTTTTTT[C/T]GTTGTTGTTGAGATG | 114792 |
| rs560444642 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047967 | CCACAATAAAGTTTA[C/T]TGTTTAACACTCTGG | 114792 |
| rs560452997 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112515 | GCAATGGTGGGATCT[C/T]AGCTCACTGTAAGCT | 114792 |
| rs560473721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022118 | GTCTGTTTCAATACT[A/G]CAGCCCCAGTGAACC | 114792 |
| rs560480025 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086633 | ATTCCACACTGTCTT[A/G]ATAAAGAAAATATAA | 114792 |
| rs560499796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928272 | TAAATGAAAATCCTT[A/G]TAGCTATTGAAAGAT | 114792 |
| rs560510967 | in-del | -/CAT | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122288 | AGTATATTAAGTACC[-/CAT]CATCTGTGTGGGTTC | 114792 |
| rs560513188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120949 | AGCTACTCTAGTATT[A/G]AACTGAGGTGGAAAA | 114792 |
| rs560554146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015863 | TATGTGCAGCCTTGG[G/T]ACTTGGTCCCCTGCA | 114792 |
| rs560557421 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920547 | TCTCCTCCTGAGCCA[A/G]TAAAATGGAAAAACA | 114792 |
| rs560569158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957866 | ATGTAACATTATTTT[A/G]GGGAATGAATTTCGT | 114792 |
| rs560573003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050578 | GGTGGGGCTTGAAAG[A/C]CATCCGGAGTGAAAT | 114792 |
| rs560603446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905880 | AGAACCATTTAGCTG[C/T]CTGAGGCTGTTTTTA | 114792 |
| rs560622996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137596 | CTGGAGTGCAGTGGC[A/G]CGATCTTGGCTCACT | 114792 |
| rs560637861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043431 | AAATAGCAGTATGTT[A/G]TGTATACATACCATC | 114792 |
| rs560640988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913138 | TCTTGCTAAGATTAG[A/G]AAGGACTATTAATGA | 114792 |
| rs560681574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016999 | CCTCCCCAGCCATGT[A/G]GAACTGTGAGTCAAT | 114792 |
| rs560691382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037230 | TTCTAACAGTGAAAG[A/G]TTTAACTATAAATTA | 114792 |
| rs560696239 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956753 | ATTCTTATAATGTTC[A/G]ATTGTTGTAAGAATT | 114792 |
| rs560704656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904857 | GTGATGTAAGGATAT[A/G]ATTCTTTCCCCATAA | 114792 |
| rs560751542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985900 | TCTCCGTCCAGCTTT[A/G]TTCCATTGCTGGTGA | 114792 |
| rs560768842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017624 | ACTATTCTGGAAATT[A/G]TAGAAACAAGAGTGT | 114792 |
| rs560804369 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078661 | ATTTTTCTTTCACAC[A/G/T]TCAGTGGCATTCTCA | 114792 |
| rs560833852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929775 | GTTTTGGTGAGATTT[C/T]TAAACGAACTATGTA | 114792 |
| rs560839397 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923345 | TATTCGATTTTCTGA[C/T]AGAAGACAACGCAAT | 114792 |
| rs560842409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942003 | AGAAAAAGACTGGCA[C/T]ATGTACTGTATATAT | 114792 |
| rs560848822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989462 | GTTTCTTTTGAAAGG[C/T]ATGCTGTTAGCTTGA | 114792 |
| rs560895643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980474 | ACATTTATTTATTTG[A/C]ATATAGTGAACCAAC | 114792 |
| rs560916975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045722 | TTGATGTGTATGTGC[A/G]TGTGTGTGTGCACGC | 114792 |
| rs560930853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985717 | TGCCTTGGTTTTCAG[A/T]TCCATCAGGTCCTTT | 114792 |
| rs560931023 | in-del | -/A | 0.232266 | 0.24937 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950502 | TCAGTTGTCACGTTA[-/A]AAAAAAAAAACCCAG | 114792 |
| rs560937188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947564 | GGTTATCACATCTCT[C/T]CTCTGATGCTTTTAT | 114792 |
| rs560956270 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092155 | CACACACCTGGCTAA[-/TT]TTTTTTTGTATTTTT | 114792 |
| rs560985582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065003 | AGTGACCATGCACAG[A/G]GTTCCCTGCAGGAGC | 114792 |
| rs560990068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928970 | AAATCTAGACAGAAG[C/G]CTTTGGTGACAGATA | 114792 |
| rs560990922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038397 | TATACAGATGTCCAA[C/T]AGATATATTTAAAAA | 114792 |
| rs560999901 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953599 | TGTACCACTGTACTC[C/T]AGCCTGGGTGACAGA | 114792 |
| rs561018408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974160 | AGTACCTGCCTCATG[G/T]TGTTGTTGTGCAGAT | 114792 |
| rs561046990 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908788 | GTCCTGCCCCCTCCC[C/G]TTCACCAGTTTCTGG | 114792 |
| rs561061033 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955990 | CAATTTACAAAAGAC[A/G]GATGTTTATTGGACT | 114792 |
| rs561076927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003847 | CTGTTCCGTTGGTCT[A/G]TGTCTCTGCTTTTGT | 114792 |
| rs561082526 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101060 | CAATCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 114792 |
| rs561097861 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906760 | GAATAAGTATAGTCA[C/T]CTATTTTTTCTCATT | 114792 |
| rs561119081 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943822 | AAGTCATATCTGGCA[C/G]GGGAACGAGTGTGCA | 114792 |
| rs561125067 | in-del | -/A | 0.195055 | 0.243887 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038327 | ACAGTTCACTAGCAA[-/A]AAAAAAAAAATCCAA | 114792 |
| rs561133827 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932386 | CACCTACAGATGGGG[C/T]CTCCTAATAGAGCAA | 114792 |
| rs561145413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073891 | CCTCACTGTCTATCC[A/G]CAAGTATCTTTTAGA | 114792 |
| rs561157772 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937968 | GTGAACCGTGTCTCC[A/T]TCTCAGACTCTGTAA | 114792 |
| rs561160272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009793 | CAGTTTAAAAAGCAC[A/G]TGAGGGTCTTCTTAA | 114792 |
| rs561161382 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139417 | TTTAAGCAAAAAATG[A/G]ACAATTTTCTAAAAT | 114792 |
| rs561170173 | in-del | -/AAAA | 0.0023933 | 0.0345097 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898695 | ACAATAAGACGTCAG[-/AAAA]AAAAAACAAACAAAC | 114792 |
| rs561198029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087849 | TCAAATTAACCTCAC[C/T]GAACCAACTCTTTTT | 114792 |
| rs561205813 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905685 | AGTAAACATTCAAAA[-/T]ACTATTAGCTATTAT | 114792 |
| rs561206263 | snp | C/T | 0 | 0 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899077 | AATGTAATCATTAAG[C/T]ATAATGCTTAATCAG | 114792 |
| rs561207887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094474 | AGTGGCCATTCTGAG[A/T]TCATAATCAGGAGAA | 114792 |
| rs561237438 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907027 | CAAAAAGATAATTCA[G/T]GTACCTAGCTAGCTG | 114792 |
| rs561240999 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929061 | TATGAAAGAAATGTG[A/G]CAAGCAAGTGGGAGT | 114792 |
| rs561261353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080673 | AAGTGTGGCTTGAAC[A/G]TACCTGGCATTGTTC | 114792 |
| rs561264320 | snp | A/G | 3.63901e-05 | 0.00426541 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976191 | GGGTAAGTCAGCATT[A/G]TTTGTTTCTCGTAAA | 114792 |
| rs561294183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032628 | TCCTGCTGTATATAC[A/G]GGATTGGTGGCAAGC | 114792 |
| rs561314219 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986597 | TCCCCCAGCCTGGCT[C/G]CTGCCTTGCAGTTGG | 114792 |
| rs561342037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997755 | CAACAACAAAAAAAA[A/C]CATACAAGAGATCCT | 114792 |
| rs561347146 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939011 | TGGATGTAGGGTAAT[A/G]TGAATGTAGGCAGTC | 114792 |
| rs561351884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982532 | CTTTTAATTGGGGCA[C/T]TTAGTTCATTTGCAT | 114792 |
| rs561355944 | in-del | -/TA | 0.00761054 | 0.0612156 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142188 | ATACTTTTATTATTA[-/TA]TATAATTTTATCATA | 114792 |
| rs561359182 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083644 | AGTATATATACAAAA[A/G]CATTAATAGTGATTA | 114792 |
| rs561372544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931556 | GCTTATACCTGGTAT[A/G]GATGTATGCATATGT | 114792 |
| rs561376836 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991097 | AGACTGGGCTCCTCT[C/G]CTTATGGCGGTTTTG | 114792 |
| rs561388306 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968385 | AACAAAAAACAAAAA[A/C]AAAAACAAAAAAAAA | 114792 |
| rs561426958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096056 | TTGCTAAATATTGCA[C/T]GGAAAATTCAAGACT | 114792 |
| rs561436688 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986301 | GGGGGGGCCTCCCAG[C/T]TAGGCTACTCAGGGG | 114792 |
| rs561476446 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96899924 | AATATCTTAAGATAC[C/T]AATAAACCCAGGGTC | 114792 |
| rs561479230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109887 | TAGAATTACTTGACT[A/T]AATTAGGAACAATAG | 114792 |
| rs561495779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116027 | ATAACCAGGAAGATA[A/G]TCACAGGCTCAGCTT | 114792 |
| rs561532770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992208 | CAGCTGCCGGTGTCC[A/G]GTACCAGGGGATCCA | 114792 |
| rs561547794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103317 | TTCCCAGGTTCATGC[A/G]ATTCTCCTGCCTCAG | 114792 |
| rs561552922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089845 | TTGAGGACACTTCCT[A/G]CTTGTATTCTGAGTC | 114792 |
| rs561556956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116882 | ACATTTTCTTTGTTC[C/T]TCTTTTGCACTAATA | 114792 |
| rs561558719 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069821 | AAAAATACTTTCTTC[A/G]GGGATTAAATTTGAC | 114792 |
| rs561559870 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097256 | ATCAGACTCCTCCAT[C/G]ACCGAGCTGTCACTC | 114792 |
| rs561563096 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018549 | GAGGTTGCAGCGAGC[C/T]GAGATCACACCACTG | 114792 |
| rs561581269 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924422 | GGGCGGCGTGGAGGA[A/G]GGTACTTCCGGGACC | 114792 |
| rs561604309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960804 | GGTATGACAGCTGGA[A/G]GCGGGGGCTTCTGGG | 114792 |
| rs561621655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992610 | CGTATCAATACGTGC[A/G]CGCATGTGAGTGCAA | 114792 |
| rs561632436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099674 | TGCATGACTGCTGCA[C/T]GCTGGGCTCTCTGGG | 114792 |
| rs561633235 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935683 | GTCTAATGTGTATTT[A/C]TAACTTGTGTATTAA | 114792 |
| rs561639644 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932544 | CTCTCACCTTGTACT[G/T]TTTCACAAAGTTGTC | 114792 |
| rs561645692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060287 | TTAAAGACAGTCCCT[A/G]CCAGCCACCAATCCA | 114792 |
| rs561646216 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125793 | AAAAAGAAAAAGTTA[C/T]CGTCCTACATTCCCA | 114792 |
| rs561687260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012705 | TGTAATCCTGGTCTC[A/G]TAGTGCCACCTGAAA | 114792 |
| rs561688200 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009655 | TTGAACATAATTTGT[G/T]TACTACTTTGAATTC | 114792 |
| rs561693272 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102331 | AGGAAACAATGGGGG[C/G]TGTTGTGACCCACAT | 114792 |
| rs561704603 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118059 | CCTGCCCTCTAGGAG[A/C]TGGCAATCAAATAAT | 114792 |
| rs561706526 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126342 | TTACTATGCTGTTTT[A/G]TGTTTTTTTTTTTTA | 114792 |
| rs561707032 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141064 | TGAACTCCAGTATTT[C/T]AGAAAACTTTTCAAC | 114792 |
| rs561745131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987783 | GAACAGAACAGAGCC[C/G]TCAGAAATAATGCGG | 114792 |
| rs561751250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019726 | AACCGTAATAAAATA[A/T]TTGGAAGTAAATAAG | 114792 |
| rs561764599 | in-del | -/ATTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025983 | CTAGAAGAAAAAACT[-/ATTT]ATCTTTCTTTTAATG | 114792 |
| rs561768355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909830 | TGTGATTTGAACACA[C/T]TAAAAATTAGAAATA | 114792 |
| rs561768690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133085 | ATCCCCCAAGCTTTA[A/C]AAATACTTCCTTTCC | 114792 |
| rs561776277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047388 | AGGCCATTATTACAG[C/T]AGAACCAATGGTGGA | 114792 |
| rs561784715 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004946 | TTTCTTTCTTTTTTT[-/A]TTTGTTATGGGTCTG | 114792 |
| rs561805776 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082333 | ATAAGCTCAGTTTAG[G/T]CTGGGAGCGGTGGCT | 114792 |
| rs561805807 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947329 | CTCTGGTTCCAAGTG[-/A]TGCCCAATTCATGAA | 114792 |
| rs561821776 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970821 | CATTTTAAAGTGTTT[A/G]TAAATTATAAAGTGT | 114792 |
| rs561829074 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910577 | ATATGTTTAATTGTA[C/G]TTAATTTGCAAACTG | 114792 |
| rs561830731 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140338 | TGCTTTGACATAAAT[C/T]TGAACCTAGAATTGG | 114792 |
| rs561835152 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048067 | AAGGGTTGAAACCTA[A/G]TTAGCTTCCTCTTAA | 114792 |
| rs561835398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001470 | TGTTTTGGTTTGTTT[G/T]TTTGTTTGTTTGTTT | 114792 |
| rs561838012 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020438 | TATAGAAAAATGTAA[C/T]TATCAAAAGTGGGCC | 114792 |
| rs561867418 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945145 | AGAGGTTGGATGCAG[A/C]TTCCATTACTTAATT | 114792 |
| rs561870585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006431 | TGGGCCTCTTGAAGC[A/G]AGCATACAGTTGGGT | 114792 |
| rs561875246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014259 | GAAATCGCGCCACTG[C/T]ACTCCAACCTGGGTG | 114792 |
| rs561880137 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988703 | AGACTTGGAACCAAC[A/C]CAAATGTCCAACAAT | 114792 |
| rs561902793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027803 | CAGCCTACAAAACTT[C/G]GAGCATTGGCTTCAA | 114792 |
| rs561920180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918964 | CCCTTTCCCTTATGG[A/G]GGTAAGAGAACTTCA | 114792 |
| rs561954273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945711 | TAGGAAATGGCATTC[C/T]TGGGCAGTGTCTTCT | 114792 |
| rs561967570 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948887 | TTTTTCTGACTCATG[A/C]GAAAAAGTCATGTAG | 114792 |
| rs561968428 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977416 | ACAATTATTAGCCAG[A/G]ATGTTTTGAAACATT | 114792 |
| rs562013680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134013 | ACTTAACAAAAAAAA[A/C]CCCCTACATAACTGG | 114792 |
| rs562018673 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958907 | GATGGAGTGTTGGGA[C/G]GTGATGGTGCTTCAA | 114792 |
| rs562024343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111399 | TTCACGGGCGGGAAC[C/T]GGAATGCGGGTGCTG | 114792 |
| rs562030784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911692 | AAAGCACAACATAAA[A/G]TTCAAACTGCTAAAT | 114792 |
| rs562033194 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919587 | ACAATATTTAAGCAA[A/T]TTTTTTTCTGACTGT | 114792 |
| rs562041352 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917951 | GGGGCTGTTCCGTAC[A/G]TTGTAGGATGTTTAG | 114792 |
| rs562042520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926240 | TTTCTACTTCTTGTT[A/G]AATGACCCAAGGAAA | 114792 |
| rs562047119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912340 | CTGATTAACCACCAA[A/G]CAGATAAACCTTGCT | 114792 |
| rs562059045 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068276 | AAGTATCATTGTCTT[G/T]TTAATAATATGCAAT | 114792 |
| rs562079030 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045786 | CTATGAAATGTGAAC[C/T]GAAGTGAAGATAGCA | 114792 |
| rs562079836 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960981 | CCAGGTAGAGGCTTC[A/G]GAAAGAATAGATTGT | 114792 |
| rs562081008 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023451 | TTAAAACTAAATATA[C/T]ATTTTTTGTTTTTAT | 114792 |
| rs562082577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034583 | GGGGTTGTGTTGAAT[A/G]TATAGATCATTTTGG | 114792 |
| rs562089938 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007147 | AATTGTAGATTTGGT[C/T]TCTTTACATTATCCC | 114792 |
| rs562099159 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004538 | AGTGGTGAGAGTGGG[C/T]ATTCTTGTCTTGTTC | 114792 |
| rs562120093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068953 | CCTGCAAGAGGAGGC[A/G]TGCTGCTGGGATGTG | 114792 |
| rs562132973 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958823 | CTGGGTAGAAGGAGT[A/G]CCAAGGAAAAAAAAA | 114792 |
| rs562141252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984120 | ACATCTTTATTTCTG[C/T]CTTCATTTCGTTATA | 114792 |
| rs562153295 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983717 | GTATTTCTGTGGGAT[C/T]GGTGGTGATATCCCT | 114792 |
| rs562159217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007247 | TGGAGAGGTAGTCTT[C/T]GAGTTCTGAGACTCT | 114792 |
| rs562178465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043311 | CATATAAGTGAGATC[A/G]TGAAGTATTTGTCTT | 114792 |
| rs562187503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061962 | CCATAAGTGAGAACA[A/G]CTGTCCTGGTAGGGT | 114792 |
| rs562196047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000638 | TTGTGCCATTTTCTA[A/G]ACATCAAATAAAACT | 114792 |
| rs562223252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926757 | CCACTCCACTGTAGC[C/T]GATTGTTACTGTCCA | 114792 |
| rs562235716 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067154 | GCTCCAAGGGAAACC[A/G]TTGGTGGAAGCTCCC | 114792 |
| rs562244440 | in-del | -/TGAATCCATT | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980774 | GGTAGAAGTCAGCTG[-/TGAATCCATT]TGGTCCTGGGCATGT | 114792 |
| rs562248272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062469 | TCTGACTAGATGGAA[A/T]AGGAGATATAAAGAT | 114792 |
| rs562264948 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120098 | TGAGAGCATTTCCCA[A/G]GTACCAGGAACAGTG | 114792 |
| rs562265798 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104657 | CATAAGTCTGTAGTC[-/A]AGCTATAATGGTTAA | 114792 |
| rs562271535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941096 | AGCCATTATTTCTTC[C/T]TTTGTACTTTTGTAA | 114792 |
| rs562295496 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069495 | TCTTGAAATACCTAC[A/G]TCAGGGCTGAAGGTA | 114792 |
| rs562310579 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129095 | ATTATATGTTCAAAT[-/G]GGGGGAACAGATAAA | 114792 |
| rs562311180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971089 | GTTAAGAAATGAGAA[A/T]CTTTATCCCACTTAG | 114792 |
| rs562318724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135187 | AGTCAGCATGATGGG[C/T]ATTTCTGTGTTCCAG | 114792 |
| rs562325604 | snp | A/G | 0.000848948 | 0.0205853 | intron-variant, synonymous-codon, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105451 | TTTGCAGAAGTGTGG[A/G]ATTTGTGCTGCCTTT | 114792 |
| rs562339030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070506 | CTAAGCCCACACTAA[A/G]GGATGTCAGGAAGCG | 114792 |
| rs562366738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007706 | TGATTGTGCTATAAG[A/G]TAGGTACAGTCAACT | 114792 |
| rs562394703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935415 | CTTTTCCCCCCATAA[A/G]GTAAGGTAAATGCTG | 114792 |
| rs562420494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904566 | GTGTAAAAATGTCAA[C/T]TATTCAAAAAATTAA | 114792 |
| rs562422634 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028975 | GGATCTGAGAGGGCA[A/T]CCCAAGGCTGAAGTC | 114792 |
| rs562443033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984654 | TCTCTTTTGATCTTT[A/G]TTGGTTTAAAGTCTG | 114792 |
| rs562452651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001146 | CCATAGAATATACAA[C/T]ACCAGGAGTGAACCC | 114792 |
| rs562458045 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971987 | CCTCCTGAGTAGCTG[C/G]GATACAGGCATGCGC | 114792 |
| rs562461371 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912498 | CTCTTTTCTCCATTA[G/T]CCCTTAAAATGGCAA | 114792 |
| rs562466339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064206 | TATGCCCCTTTCCCT[A/G]AAATACCTGTTTCTG | 114792 |
| rs562468647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955653 | GATAAAGACATACCC[A/G]AGGCCAGGCACGGTG | 114792 |
| rs562470741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903650 | AACTTAATTTTGCCA[A/G]TGACCAAGTAAGCCT | 114792 |
| rs562475366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091630 | GCCAAGTTGGGGCAC[A/G]TTGAAATGATATGGG | 114792 |
| rs562492888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973026 | TTGTTGATTAAGAGG[C/G]CTTTATTTCTTGCCA | 114792 |
| rs562518145 | in-del | -/TAATA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905721 | TATATAACAAAATAC[-/TAATA]TAATAGGAAACATTT | 114792 |
| rs562537711 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078461 | GATGAAACAAAGCAT[G/T]GTTAAAATAGCCACA | 114792 |
| rs562541788 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135597 | GCCACTGCATCTGGA[C/T]GATTTGTTATTAAGA | 114792 |
| rs562581012 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908331 | ATACCAAAACCTTGC[A/C]ACACACAGAGGTGTT | 114792 |
| rs562583118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989014 | ATGTTAAATGAGAAG[C/T]TAATGGGTGCAGCAC | 114792 |
| rs562594663 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099365 | CTCTTCAGTGTGGCC[C/T]TCTCTATCTTCAGGG | 114792 |
| rs562597823 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071105 | AGGAGACACTCTTCT[C/T]CATCTCTCATTACCG | 114792 |
| rs562600616 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909210 | GTAGGGTTAGAGAAT[C/T]CGGCATCCCTATCAG | 114792 |
| rs562616535 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938703 | GGCCTAAGCTTGAAT[A/C/T]CTGGTTCTTTCATAT | 114792 |
| rs562617292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966483 | TTCCTACTGATTTTT[A/C]TTCTCTCTCTATGTT | 114792 |
| rs562617350 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028027 | TATTTCTCCAGCAAG[A/G]GACAGCCTGTCATGA | 114792 |
| rs562652228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928826 | TTCTAGTAGAGTCAT[A/G]GACTTGGAGGCTAAG | 114792 |
| rs562656219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980286 | CTATTCAGTATGATG[C/T]TGGTGTGGGTTTGTC | 114792 |
| rs562689394 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006295 | AATTGTTGTTGTTGA[G/T]TTATAGTCTTTTTTG | 114792 |
| rs562692730 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985164 | ATGAAATTCTGGGTT[A/G]AAAATTCTTTTCTTT | 114792 |
| rs562705802 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076077 | TGTGCCTTTTCTGCT[A/T]TGAGTAATATAGAGC | 114792 |
| rs562707645 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903081 | TTTCTTTAAAGGACT[A/G]AAGATAAAGCAGAAA | 114792 |
| rs562708578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022180 | GCTCAAACCCTATGA[C/T]GGTTTCTACTCTTAT | 114792 |
| rs562715550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921502 | AAAACTAGAGAACAT[C/T]AGCCAAAAATCAATT | 114792 |
| rs562719251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989512 | GTGATTTGCCCTTTA[A/T]CTCTAGCTGCCTTTA | 114792 |
| rs562728965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979672 | CATATGAATTTTAGA[A/G]TAGGTTTTTTCTAAT | 114792 |
| rs562735803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086207 | TTTAAAGTCTTCTAT[C/T]AGCTGATTAAACAGT | 114792 |
| rs562735914 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105175 | TTATAAAATAATATC[C/T]AAAACAATGTACTTT | 114792 |
| rs562742813 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030292 | GTACCACCCTAAAAT[A/G]TAGCTGTAACTAATC | 114792 |
| rs562754763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113283 | CTGCTAGTGTTATGT[G/T]GACTTTCTCTCAAGT | 114792 |
| rs562797116 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008634 | TGGGGTCTCCTGCTG[A/G]TAGGATTCTGGAGAT | 114792 |
| rs562799607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928299 | AGATGGGAGTCTCCA[C/T]CAGACAGTCTGTTGG | 114792 |
| rs562800804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016360 | CCACCTCTTGCATCA[A/G]TGTGCCTTAGATGTG | 114792 |
| rs562804656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990107 | TTCAGCCATTTCAGC[C/T]TGGTTAAGAACACTT | 114792 |
| rs562804791 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981019 | GGCGGGGGGGCAGGC[-/G]GGGGGAAAAGCCCCT | 114792 |
| rs562811603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920829 | TTTTCTCTCTCAAAT[A/G]TTACCAAGCTATCAT | 114792 |
| rs562812134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100613 | TTAAATGCAACTTGG[A/G]TACTTTCTGGACATC | 114792 |
| rs562822480 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997840 | AACCATAAAAAACGT[A/G]CAAACCAACCAACCA | 114792 |
| rs562831842 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060976 | TGCCTGCTACAAATT[G/T]CAGGAGATGTTCCTG | 114792 |
| rs562844699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107021 | TTTTGGGCTGAGCGC[A/G]GTGGCTCACACCTGT | 114792 |
| rs562854397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985970 | TTAGAGTTTCCAGCT[A/T]CTCTGCTCTGTTTTT | 114792 |
| rs562884438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009164 | GGTCTGAAACATACT[A/G]GATGTTAAACTGATG | 114792 |
| rs562894130 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041416 | AACTTTTTTTTCCCC[C/T]AGTCTCTCTAGAATT | 114792 |
| rs562913317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044783 | ATTTCTTCTAGATTA[C/T]CCAATTTTTTGGTGT | 114792 |
| rs562933202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986255 | CTCAGAGGAGTATCC[A/G]GCCGTGTGAGGTGTC | 114792 |
| rs562946001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949992 | CTTGCTGTTCAGTTA[C/T]TCTGTAAAAAGCAGG | 114792 |
| rs562948570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051387 | AATGGTTTTATTGTC[A/G]TAGGTGGGGCAATAA | 114792 |
| rs562955490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913776 | ATATGTGCACCTTAA[A/T]AACTAGGGCTCTCCT | 114792 |
| rs562962419 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897920 | GCCGCGGGCGCTTAA[A/G]TGCGTGCCCGTCGCC | 114792 |
| rs562979868 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136855 | GGAAACCAGACAAAA[C/G]CTCTCTGGATGATTA | 114792 |
| rs562981877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044171 | ATACATTCTTTCTAT[A/G]CCTAACTTGTTGAGA | 114792 |
| rs563023890 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036716 | GGGGTGCCAGGTCCT[A/G]GTGCAGGTGTAAGAC | 114792 |
| rs563031499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906869 | CTTAGAGGTTCCCAA[C/T]CCACAACCATGGGCA | 114792 |
| rs563037992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995696 | GTAACTTCCTGTTCA[G/T]CTCTTAGTCTACCCT | 114792 |
| rs563039670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969136 | CCTCATGTCAGCCTG[A/G]AGGATATGTCTGCTT | 114792 |
| rs563042312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137821 | ACAGGCATCAGCCAC[C/T]GCGCCCAGCCTATTG | 114792 |
| rs563056233 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897440 | AGCACTGGCTGCTGC[C/G]TCTGGGTCTCGGAAG | 114792 |
| rs563072676 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079909 | TCAAGAGAGTTTCTT[G/T]TTGCTGAGCTGTAAT | 114792 |
| rs563080041 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025117 | GTTTTACAAAAGAGG[A/G]GAAGACATCTGATCC | 114792 |
| rs563082537 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027639 | ACCATTCACAAGCTT[A/G]GGATGATTTACTCTT | 114792 |
| rs563100394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122628 | GTGAAGTTATAGTCT[C/T]TCAAGAACTGGAGAA | 114792 |
| rs563133238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072851 | ATATTGTTTGTGTTA[A/G]TTTACTTATCTGTCT | 114792 |
| rs563152570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030983 | TGAGAAAAGGAGATA[C/T]GGCACCTGCCTTCAT | 114792 |
| rs563156301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004023 | TCTGTGAAGAATGCT[A/G]TTGGTTGTTTTATAG | 114792 |
| rs563161407 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003565 | TCATGAAATGTCTGC[C/G]AGGGCCTATGTCTGA | 114792 |
| rs563163746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981811 | ATTTCATTGTTTACC[C/T]GAAAATCATTCAGGA | 114792 |
| rs563193100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004950 | CTTTCTTTTTTTTTT[A/G]TTATGGGTCTGCTAG | 114792 |
| rs563203348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936449 | ATCCAGAGCCTCTCC[A/G]TTTTTGGTTGTTCAG | 114792 |
| rs563222829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943125 | ATATACACATACCAG[C/T]ATATAGACACATATG | 114792 |
| rs563241974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031754 | AGAAGTCTAGGAGTA[C/T]GTTGCAAAAGTAAAG | 114792 |
| rs563248699 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923420 | CACCTAATGTTTGTA[C/G]TCAGTTGTTTGTCAT | 114792 |
| rs563250178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031381 | CACTCTTTTGCCCAA[G/T]CTGGAGTGCAGTGGT | 114792 |
| rs563277832 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964280 | GCAAGGAGGTGGGAA[A/G]AGGGAGAAGAAGTGT | 114792 |
| rs563279887 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971800 | GAACCATAATGAGAA[A/G]CATATCTATAATTTA | 114792 |
| rs563288320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937045 | TTTTCCCCACAGCTC[C/T]TATCGATTAAAAAAA | 114792 |
| rs563288367 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054158 | TCAGGATAAATAATT[A/T]GCTAAACAGTACTTT | 114792 |
| rs563295886 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142036 | CATAGTTTTACCACA[A/G]AGTATAAAAACATCA | 114792 |
| rs563313708 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139986 | AGGATTAGGCGAACA[A/C]TTTGTAATACTTTGC | 114792 |
| rs563317416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039356 | CTCATGAAGACATAG[A/G]GTAGATTGGTGGTTA | 114792 |
| rs563331171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974214 | CACTGAGAATAGTTC[A/G]TGGGACACGGTAAGC | 114792 |
| rs563331573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065592 | GTCACCTTCACTTGC[A/G]TTTATTATAGCATTA | 114792 |
| rs563346880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102665 | GGGAAATTATAGGGT[A/G]TTATTCTATAACTGT | 114792 |
| rs563362557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900918 | ATTTGTAGGAGTCCA[A/G]CTGAAATAATTTACA | 114792 |
| rs563370074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930657 | TGGTGTGCCGACCTT[A/G]GAGCAGAGCTACCCT | 114792 |
| rs563381440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032777 | ACTGAAATTTCTTTC[A/G]GGTTCTTTCAAGGAG | 114792 |
| rs563407503 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095204 | GTGGCAAACACACTT[C/T]AGGCTCTTTGGCAGT | 114792 |
| rs563411023 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995493 | TCCTGCTAAGGTATT[A/C]CTGAGCCCCTCACTT | 114792 |
| rs563426586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967334 | TTTTTCTTATTTAGG[A/G]TGCTAACTTCCCTCA | 114792 |
| rs563443314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101798 | AATATGTGAAGTATT[G/T]AATACTGTATAGCAA | 114792 |
| rs563447893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046577 | CAGAGTAGAAGTTGA[C/T]ACCTCTACAGCCTTT | 114792 |
| rs563449651 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975839 | AAAAGGGAGAACAAG[A/C]GAATGGTGGAGAGAA | 114792 |
| rs563458692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059987 | ATTAGACCACTCTAA[C/T]TTGCAGTTGTACAAG | 114792 |
| rs563476576 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055772 | CCCTGCACCCCAGCC[A/G]AGGTAACAGACTGAG | 114792 |
| rs563506399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094571 | AGGATCCACCCTTTC[C/T]TCTGACCACCTCCTC | 114792 |
| rs563551097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997398 | TAAAACACCCACATA[C/T]GTATGCATTGGTTAA | 114792 |
| rs563554521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959933 | TCTTTAGCACTTCAG[A/G]GTATGACTGTGTCCT | 114792 |
| rs563572837 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932578 | TTCCCCCCCCCCCTT[G/T]TTTTTTTTGAGACAG | 114792 |
| rs563603859 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087974 | AAAATACCCCAAGAT[A/G]ATGCCTTGGAACTGT | 114792 |
| rs563642017 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054756 | GATAGCCATTCATCT[C/G]TATGTATCATGTATC | 114792 |
| rs563664076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080790 | ATTATAAACAAGTAG[A/G]CAAATAAATGCTGAA | 114792 |
| rs563666108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088718 | CTTGAATCTAAACAA[A/T]CCTTATCTGTCAATA | 114792 |
| rs563671317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131349 | GTGAGTTCAGGAGTT[C/T]AGGAGCATGGTCTTC | 114792 |
| rs563673190 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97047255 | TAAGCATTCACTCTG[C/T]CTTTGCACTAATGAG | 114792 |
| rs563677628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998808 | TTTCATGTGTTGATC[A/T]CAGAGGCACCAGAGT | 114792 |
| rs563696314 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026639 | GAGGGTCCACACCTG[A/G]ACTGGGCATCTATAT | 114792 |
| rs563698453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103104 | TATATATAAATAAAC[A/G]TATATAAATGTAAAT | 114792 |
| rs563702222 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108875 | TACTTCAACTTCACT[A/G]GATTTATACCTGCTT | 114792 |
| rs563703349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055566 | ACTTTGGGAGGCCAA[C/T]GCAGGTGGGTTACTT | 114792 |
| rs563710493 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067431 | TGGGCAATGTATTTA[A/C]TGCTAATTGATGGGG | 114792 |
| rs563717602 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917087 | TATCTGCCTTATTAA[A/C]TTGCAAGGATTTTGA | 114792 |
| rs563729304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081469 | TGGGAGGGGCAGTCT[A/G]TTCTCAGTCAGTGAA | 114792 |
| rs563731022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019087 | TGTAACAAAATTGAT[A/T]ATCTAGCCTCCTCCT | 114792 |
| rs563735541 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987820 | TACAACCATCTGATC[C/T]TTGACAAACCTGACA | 114792 |
| rs563797753 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990358 | GTGGGGGTTATGTTA[A/G]CAAGTATTTTTGGTG | 114792 |
| rs563802821 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038888 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCATGGCC | 114792 |
| rs563803776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954771 | GTCACTGGGATGAGA[C/T]GGACAGTAACCATGT | 114792 |
| rs563815585 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962288 | AATCCTATGTACCAG[A/T]TTATATTTGAAAAGA | 114792 |
| rs563821757 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953833 | TTTCCTGCACTACTT[C/T]TGTTTTTCATTAATA | 114792 |
| rs563859946 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966781 | AACATATTTTACTTC[C/T]TAGTCCTTGAAGCTT | 114792 |
| rs563871899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983049 | ATTGTTTTGAGATAC[A/G]TCCCATCAATACCTA | 114792 |
| rs563875076 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103821 | TCAAAACTCTCTGTG[C/G]TACAGAAACCTGTGA | 114792 |
| rs563896632 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117709 | GGTAAAATAAGCTCT[G/T]AAATATCCTACAGCT | 114792 |
| rs563905698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954517 | TGTCAGACTTCTTAG[A/G]TTTGGTGTTGGCTTA | 114792 |
| rs563908589 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97027513 | TAGCCACATGAAATT[C/T]GTCTTAAGGAAAATT | 114792 |
| rs563909087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983613 | ATTTAGTCTTGGGAG[A/G]GTGTATGTGTCGGGG | 114792 |
| rs563932152 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082505 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGCAG | 114792 |
| rs563936955 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105708 | TACTCAGCTCTTCAT[G/T]ATGAGCTCTGTGATA | 114792 |
| rs563941158 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134849 | AGTTTGTAAGACATA[A/G]AAACTTAAATAAAAA | 114792 |
| rs563952158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048200 | ATAGTCCCCTTTACA[A/G]TTCTCCACTTCCAGG | 114792 |
| rs563960102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012779 | GCAATTAAACTATAT[A/G]TGAGGGTTCTCATAT | 114792 |
| rs563971328 | in-del | -/T | 0.312837 | 0.241974 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932206 | GAACTGACTGGGTTA[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs563986908 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984352 | TGAGAAGAATGTATA[-/T]TCTGTTGATTTGGGG | 114792 |
| rs563991787 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082406 | ATCATGAGGTGAGGA[A/G]ATCAAGACCATCCTG | 114792 |
| rs563997654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019550 | TGAGTCAATCCCTGA[A/G]AAGGCTGGCAGGTGA | 114792 |
| rs564004438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987802 | GAAATAATGCGGCAT[A/G]TCTACAACCATCTGA | 114792 |
| rs564011511 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030410 | AAAGAGGGAATAACA[C/T]ACCATAAATCCACAC | 114792 |
| rs564012829 | in-del | -/GA/GT/GTGA | 0.0463947 | 0.145069 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942690 | TGTGTGTGTGTGTGT[-/GA/GT/GTGA]GATTCAGAATATCCC | 114792 |
| rs564013670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041176 | TGCATATAACTTGGT[A/G]GCAATGAGAATCCAG | 114792 |
| rs564016422 | snp | G/T | 0.00251889 | 0.0353991 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925958 | TGGTTTTTGCTTTTT[G/T]TTTTTTTTCTGATGG | 114792 |
| rs564041382 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988614 | ACTGGGTATATACCC[A/G]AAGGATTATAAATCA | 114792 |
| rs564049434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984163 | ATTCAGGAGCAGGTT[C/G]TTCAGTTTCCATGTA | 114792 |
| rs564097782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945887 | GTGGAGGCTGACAGG[G/T]TGATTATGGTTTTGA | 114792 |
| rs564161851 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111690 | ACAGCTCAGTGGAGG[G/T]TCACCCTCTTGGCAC | 114792 |
| rs564175109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133225 | GGTCTGATAGGGACA[A/G]CCTCTGTCCCAAAGA | 114792 |
| rs564178903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097235 | GATTAGGCCTGGTGC[A/G]GTTTCATCAGACTCC | 114792 |
| rs564181608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076313 | ACTATGCAAAGCTAT[A/G]GTTTAAGTACTGTTA | 114792 |
| rs564221161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118637 | AAAAAAAAAAAAAGA[A/G]TTGTAGACAAAATAT | 114792 |
| rs564223245 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901791 | CTCCATGTGTGTATG[A/T]GTTCTCATCATTTAG | 114792 |
| rs564230983 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141934 | CTAGGGTACTTTTCA[A/T]ACTTTTTCCTTCATA | 114792 |
| rs564231089 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902474 | TTGTAAATTTGTTTA[C/T]AGGCGTTGCATATTG | 114792 |
| rs564245391 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134103 | CAAAAAAATTCCCAG[A/G]ACTGTGATAATAAAA | 114792 |
| rs564246476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000407 | TTTTTGACAGGAAGT[C/G]TTTCTTGAGGAAGCA | 114792 |
| rs564252684 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032069 | AGCCTGAGGCTCAGA[A/G]AAGGTAACAAATTAG | 114792 |
| rs564268880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007797 | GCTCTAACTCTGGGG[A/G]GCTGGCAGTGGGGCC | 114792 |
| rs564283392 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993572 | AGAGGGTGTACAAAA[A/G]GGCATAGACACAAGT | 114792 |
| rs564288009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020552 | ACTTAATAGCTGATT[C/T]CTATATTACATAAAC | 114792 |
| rs564303813 | in-del | -/CAA | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999394 | AGTAAGACTCTGTCT[-/CAA]CAACAACAACAACAA | 114792 |
| rs564350075 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025760 | CTTACCAGCTTTATC[G/T]CCTTGAACCGTTTGC | 114792 |
| rs564360625 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975192 | GGATAAATGTTTTAG[G/T]TTGGGGTAGAGAGTG | 114792 |
| rs564394566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001793 | AAGATAATGAAAGCA[G/T]ATATTTTTAGATGGA | 114792 |
| rs564398038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939755 | TTTATCAGAAATGCC[A/G]AGAAGCCATTGAGGA | 114792 |
| rs564409871 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007144 | ATGAATTGTAGATTT[A/G]GTCTCTTTACATTAT | 114792 |
| rs564443873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135812 | ACGATAGAACAATTG[A/G]TTTCAATACACTAAC | 114792 |
| rs564454408 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036612 | GTGATGATGGGTGGG[C/T]TGTGTGGTAGTTCTG | 114792 |
| rs564465109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119156 | CCTGTACCTAGGTGG[C/T]TCTACCTGTGGGAGG | 114792 |
| rs564469975 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030120 | GATAAAATGGGAGTC[C/G/T]CAGTGGTTTTGCCTG | 114792 |
| rs564481438 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976897 | CACCACCGCGGCCAG[C/G]CTATATATACTCTTA | 114792 |
| rs564488017 | in-del | -/TAGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926348 | AAATAATGACAGAGG[-/TAGA]TAGAGGGGATTTATG | 114792 |
| rs564490701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934360 | CTAGAGTGCAGTGAG[C/T]TGCTCACACTCTGCT | 114792 |
| rs564507324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136512 | AAGGTGTTCTTGTTT[A/G]TTTAGTGGGTGTGTA | 114792 |
| rs564511821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062540 | GCTTAACTTTTTCAC[C/T]TCTTTACTTTGCCAC | 114792 |
| rs564512389 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027419 | ATTCTTTATGACAAA[G/T]TGAAACTTGTTAAAA | 114792 |
| rs564513538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036106 | TTCCTCTGCTTGATC[A/G]AGTCTGGTATTGAAG | 114792 |
| rs564517621 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961576 | AGAAAAGACTTTATT[C/T]ACAAGGCTGCAATGT | 114792 |
| rs564572197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056344 | TCTCCTGACCTCGTG[A/T]TCCTCCCGCCTTGGC | 114792 |
| rs564577330 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939242 | CTTATAAAAACATTG[C/T]CAGTTTTCTCAGTAA | 114792 |
| rs564600896 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985701 | TGTCACGTAGTTCTC[A/G]TGCCTTGGTTTTCAG | 114792 |
| rs564606819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913102 | ACTCTTATCAAGCAT[A/G]GGATTTGTGGCTATG | 114792 |
| rs564633044 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934899 | TGCAGGATAGTATGG[A/T]TATAGCACGATATGA | 114792 |
| rs564652577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092406 | TAAACTCATCAAATT[C/T]GTACATGTGGTCCCA | 114792 |
| rs564701514 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100148 | CTCTATCTCAAAAAA[C/T]ACATATATAAATATA | 114792 |
| rs564705938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995574 | CCCTCCCCTTTGTTC[C/T]CTTGTCTGTTTATCC | 114792 |
| rs564712907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099172 | AGGGCCTTCTTCCCT[C/T]ATACACCTGCATGAC | 114792 |
| rs564717744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964710 | GCAAATTTTAATTCA[A/G]TATATACATTTTAAT | 114792 |
| rs564737747 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017130 | TCAGTATGACTGGAA[A/T]TTGGTGAGTAAATTA | 114792 |
| rs564757779 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905457 | TTCTTAGCAGCCATG[G/T]TGTAACATAATGATT | 114792 |
| rs564765555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091873 | TGTTCATGTTTTAAT[A/G]TTTGGACCTTGGTAA | 114792 |
| rs564769682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928872 | ACAGATTTTAAGGTT[A/G]CATATACTTTTGATG | 114792 |
| rs564794995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989332 | TGCTTGTCTGAAAAG[G/T]ATTTTATTTCTCCTT | 114792 |
| rs564818392 | in-del | -/ATAGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940284 | TGAAATTGCCTAGGG[-/ATAGA]ATAGATCAATTAAAT | 114792 |
| rs564837808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058262 | CTTTAGAATCTGTTT[G/T]TTAATACACAAAAAA | 114792 |
| rs564840455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995065 | CCGTTACTTCTGTGA[A/G]CCTATGTTTTTTCAT | 114792 |
| rs564862810 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077948 | AGATAAGCTACATGC[A/G]TGAATAGCTTAGTGA | 114792 |
| rs564868691 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948528 | ATAATTATTGAAATC[A/G]TAGGATATACTTTGG | 114792 |
| rs564869516 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080078 | GATAGAGGAAATAAT[G/T]CTCTGTTGGACTGTA | 114792 |
| rs564875407 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995923 | AGAGAGATTGTGACC[A/G]ACTAAACACTAGTGA | 114792 |
| rs564900723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052133 | AAACGAAAGAAGTTT[A/G]TGTTTAAAATCCTTT | 114792 |
| rs564955716 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114016 | CAAACCACGATTCCA[C/G]TCAGACACTCTGTAT | 114792 |
| rs564964398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052647 | CCACTGCCCAATAAA[A/G]GCCAATATTGCCCAC | 114792 |
| rs564969011 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103799 | TGTTTTTCTGAAAAG[A/T]GATTTATCAAAACTC | 114792 |
| rs564983581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120902 | TTGTGCCCCAATCTT[C/T]CCTACCTCCCATCTG | 114792 |
| rs564988579 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953356 | GGTTTCTTGCCAAGC[C/T]TGTTGGCTCATGCCT | 114792 |
| rs564995088 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971625 | TTCAGGGAGTCTGGG[A/G]CTTTCCATTGTTGCA | 114792 |
| rs565005296 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071145 | CTTGCCCTCACTACC[A/C]AACTGTACCCAGTGT | 114792 |
| rs565020529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950218 | AGGTGTCTGAAATTT[C/T]TACATTTGTGTTAAA | 114792 |
| rs565031429 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090013 | CAAGTTATGTCCTAT[C/T]TTAGTGTGGCAAAGA | 114792 |
| rs565036664 | in-del | -/GAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080634 | CAGGGAAGTTGAAAA[-/GAT]GATATGGTTTCTTCA | 114792 |
| rs565058391 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118710 | ACTGAGACCACAGAC[C/T]GTGGTCACACACACA | 114792 |
| rs565061684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009737 | TGCCTGTATTTCATG[C/G]TCATACCTACTAAAG | 114792 |
| rs565089555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107063 | TTTGGGAGGCGAAGG[C/T]GGGCGGATCACGAGG | 114792 |
| rs565103774 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087640 | TGGATGGAGGGGGGC[C/G]TGCTATTTGATTAAT | 114792 |
| rs565104729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914559 | GACAAGTCACCCTTC[A/G]TTGTCATGAGGGAGA | 114792 |
| rs565106952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950990 | TAATACAAATTACTC[A/T]GTTTGAACAAAAAAA | 114792 |
| rs565110446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016459 | TTGCATGGAACTGTA[A/G]CTCCTTTATTTTGGC | 114792 |
| rs565120682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973196 | ATCCTGTGAAATTGT[A/G]CAGCATCACTATTGT | 114792 |
| rs565136681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009287 | TTAAGGCTATTCAGC[A/G]GAGACAATTTTTACC | 114792 |
| rs565163702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107613 | TTGCCAAGAATCTCA[A/G]ATAGAAGTGGCCAAC | 114792 |
| rs565189817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913886 | AGTCTATGGATAGAT[A/T]ATATTACCTGACAAA | 114792 |
| rs565190961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073018 | ATTCAATGAGATAGT[C/G]CATGCAAAGTATCTT | 114792 |
| rs565191019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080486 | ACAATCTTTGCTTCC[A/G]AGAAGCTTAGATTTG | 114792 |
| rs565224537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045482 | TGGGATGAAATAGTA[A/G]TTTTTTTTTTGTAAA | 114792 |
| rs565227427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100949 | CTGGACCACAGGCAT[A/G]TGCCACTGCAGCCAA | 114792 |
| rs565228900 | snp | C/G/T | 3.29496e-05 | 0.00405881 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113931 | GTGAGACTGCAACAG[C/G/T]CCTTGTCAACGAGGC | 114792 |
| rs565243845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981888 | CTAGTATTGATTTCT[A/G]TTTTTATTACACTTT | 114792 |
| rs565261520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086959 | ATCTCTTTTTGTGGC[A/G]CAGTTGAAGGCACTG | 114792 |
| rs565263415 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935034 | TAAGCACCAGTATAC[A/T]GATAAGAAGAAAAAG | 114792 |
| rs565290515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108659 | TTAGATTCTTATGAA[C/T]GTAAAAACAGAGCAC | 114792 |
| rs565309399 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044923 | CTTAGTCTGGCTAAA[G/T]TTTTGTTGATTTTAT | 114792 |
| rs565316827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990593 | GCTCAGGCTTTGTGT[A/G]TCCTCTCCAACTTGG | 114792 |
| rs565320303 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137909 | TAGATCATTAAAGAC[A/G]CGTACAAAGAGGTCT | 114792 |
| rs565332520 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003819 | TATGTGGCTTTATTT[C/G]TGGTTCTCTATTCTG | 114792 |
| rs565336026 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996335 | GGCGTGCTCCTGCCT[A/G]TGTAATTTTTAGAAT | 114792 |
| rs565336132 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944861 | TCTGAATCTATTCTT[C/T]ATCGAAGAATAAACA | 114792 |
| rs565342441 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086367 | CTTATTTCATTATTT[G/T]TGTTACTTTAATCAG | 114792 |
| rs565347303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943321 | TTAAAGGGTTGGTCT[C/G]TTGGTGTCATTCACA | 114792 |
| rs565355985 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003553 | TCGGCATCTTTGTCA[G/T]GAAATGTCTGCCAGG | 114792 |
| rs565364787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037558 | AAGGGAAAGATACTC[C/G]GTATTCATGGATAGG | 114792 |
| rs565381643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138433 | GGTCCTGGCCACTCA[G/T]GAGGGTGAGGCAGGA | 114792 |
| rs565395953 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923859 | CGGTGGTGGAATACT[C/T]ACCTATTAAAATTAC | 114792 |
| rs565396709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996684 | TATCCCTTTTCCTCT[C/T]TTCAACATTCTCAAG | 114792 |
| rs565410498 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986284 | TCAGTCTGCCCCTAA[C/T]GGGGGGGGCCTCCCA | 114792 |
| rs565430708 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123479 | GTTTTTAAAGACTTA[G/T]TTGACTTTGGGGGAC | 114792 |
| rs565438265 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898186 | GAGTGAGGCCCAGCA[C/T]TGGATAAGACTCCAC | 114792 |
| rs565439474 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898854 | AAGGAAGCAGTAGGA[A/G]GGAAGTTACAGTATT | 114792 |
| rs565481822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96997451 | TCAGAAAGTGTCCTA[C/T]AAAGACTTGAAGGTG | 114792 |
| rs565485597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033451 | ATTAAGATTGTTTCC[A/G]TATTGTGGCTATTGT | 114792 |
| rs565502286 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899319 | AGGGCTTTTTAGGCA[C/T]GGTATTTCTATTTCT | 114792 |
| rs565507674 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131011 | TCACCAAACTTGTTT[C/T]ATAGACATCTTTAGG | 114792 |
| rs565514367 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130607 | ATGTAAGAAGCCCAT[A/T]CCTTTCAATATATAT | 114792 |
| rs565558293 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901211 | CTGCTAGCAAATTAC[C/T]GCAAATGGTTTAAAA | 114792 |
| rs565561433 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115041 | GCTGTTTCAGATAGG[G/T]TCTCACTCTTGTTAC | 114792 |
| rs565580984 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022262 | ATCCCTCCTACAACT[C/T]TCAACCTCCGTCCAT | 114792 |
| rs565584433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032202 | GTTGTTTGAAATACA[C/T]AAGTAATACATGTTC | 114792 |
| rs565586084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065780 | TTATCATTGACTTCT[C/G]TTACCTCTTAGGTAG | 114792 |
| rs565595500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930784 | CTCTGACAAGCCACT[C/G]TTCCCTCTTTTATGC | 114792 |
| rs565614282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025720 | AATGGTGGTGAAGGC[A/G]TGGGTTCAAGTCCCG | 114792 |
| rs565615666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094776 | GTATTGGTAAGTGGC[A/G]CGGTATTACTTATGC | 114792 |
| rs565619977 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993764 | CTCATAATGGCAGTA[A/G]TAATCAAGTCTCAGC | 114792 |
| rs565621104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025492 | TTCATGTGAAATTCC[A/C]GTAATAGATATGAAT | 114792 |
| rs565631445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907338 | TTTTTAAAAAATCCT[C/T]CTTTTAGTGATACAT | 114792 |
| rs565638960 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124002 | GATTAATCTAAAAGC[A/G]AAGAGTGTTATGTGA | 114792 |
| rs565653930 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138895 | TTAAATGCTTATAAA[A/T]ATACATGTATGTATA | 114792 |
| rs565660971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052404 | CAAAGTAACAGTCTT[C/T]TCTTTGTTTTTATGG | 114792 |
| rs565682154 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970322 | CAGGCCTCTGCTGCT[C/T]GGGCCTTACCTGCAC | 114792 |
| rs565686244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087459 | AGACAGATCTACAGA[A/G]TCTCATTAAATTGCT | 114792 |
| rs565689468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011219 | GGTCATTTAACAAAA[C/T]TGCTGTTTATTAAGA | 114792 |
| rs565736250 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967603 | TCCTTTTAATAATTC[A/G]TTTATTTAATAGATA | 114792 |
| rs565759497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915711 | GAGTGAGAATTAATA[A/C]TGCTCTGTAATTGGA | 114792 |
| rs565788695 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924867 | CACGCTAGGACGCTC[G/T]TCTTCGCTACTGCAT | 114792 |
| rs565789031 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915896 | TAAAAGCAGGACATA[A/C]ATTTGCCTTTATAAA | 114792 |
| rs565845398 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139606 | CAACATAACACTGTT[A/C]GTAAGGCAATTTATT | 114792 |
| rs565856835 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054140 | GTCAAATTGTAATTA[A/C]TATCAGGATAAATAA | 114792 |
| rs565860649 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920932 | ACTGGACCAAAAAGT[A/G]TGAGCTTTTAAGAAA | 114792 |
| rs565877319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914003 | AACGTAATGAGAACC[A/G]TCCTTAAAAGTGGAA | 114792 |
| rs565879744 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088004 | TTCTTTTTTTTCCAT[A/C]TGACCTTTCTAAGCT | 114792 |
| rs565894291 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080289 | AAGGCCTGTGAGATA[C/T]GAAAAATGGCCTGAT | 114792 |
| rs565904669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116323 | ACAGTTAATAACCAC[A/C]AAGACTATATTCTTT | 114792 |
| rs565949239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032816 | CAAATTCAACATTTT[A/G]TAAACTAAAGGTTTT | 114792 |
| rs565949500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944112 | TGTTGCTCATCGTTA[C/T]ATCAAAGATGGGAGC | 114792 |
| rs565952018 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073463 | ATGGTATTGACACTT[C/T]GTAGACAGAAAATTT | 114792 |
| rs565959568 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055259 | CCATTGAGAAAATAG[A/G]AACAGAAAGGAAGAT | 114792 |
| rs565970710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109651 | AAACCGGAGGGTGTT[C/T]AGAGATGGGCCAGAA | 114792 |
| rs565975660 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083803 | TTTCCCATCCACCGT[A/G]CTATTGTTGGGCATT | 114792 |
| rs565999449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060483 | CCAGAGCCCCCATGT[A/G]AGGTGTGGGCACTGA | 114792 |
| rs566011434 | in-del | -/CA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916060 | GGCAGCCTCCAGAAT[-/CA]CAGCAGATTCAGAGA | 114792 |
| rs566012118 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060991 | GCAGGAGATGTTCCT[-/G]GGCCAGACCCAAGTA | 114792 |
| rs566016034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074146 | TCACTGAAATGCATA[C/G]TCCAGAGTAATGATT | 114792 |
| rs566031915 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083263 | GGTGCGATGGCACGC[A/G]CCTGTGGTCCCAGCT | 114792 |
| rs566037608 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938140 | TTGAAGAAATCCAGT[A/G]ACTTATCTGTATATG | 114792 |
| rs566042148 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118303 | ATCTTTTTGCAGATA[C/T]TGTTTTACTTACATC | 114792 |
| rs566055559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953224 | AGAATCTATCAATAA[C/T]GTATGTGAGAACTTA | 114792 |
| rs566067841 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919314 | GTAACTAACACAAGG[-/A]ACTCTGATTTAAAAG | 114792 |
| rs566087456 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939697 | AAATGTGCTGGAGGA[C/T]GGGTAGAGAAGGACT | 114792 |
| rs566093507 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065466 | AACTTCTTGTTAGGT[A/T]GGAGTCTGTGGGGCA | 114792 |
| rs566093946 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960311 | CTGAACAATTCTCGT[G/T]TACCGTACTTTTCCT | 114792 |
| rs566106515 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088812 | CATAGAAGTAATTCT[A/G]TATCATTCTCATGAT | 114792 |
| rs566109532 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976309 | GGGCCTTTGTTCTTT[C/T]CTGGGTAGAATGCTT | 114792 |
| rs566154141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110190 | ATTTCTTTTGCAATA[C/T]CTTTGATTATTGCAG | 114792 |
| rs566162061 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052861 | TGTTCTATAATATAA[A/C]CTTCTGATGGTATTA | 114792 |
| rs566167719 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090669 | GTACTAGATGTCAAA[C/T]AATACTATTAAAATA | 114792 |
| rs566177791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946078 | TGAATGATAAGATGA[A/G]ATTCATCTTGTTTCA | 114792 |
| rs566185560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976720 | TCTCCTGCCTTAGCC[C/T]CCTGAGTAGCTGGGA | 114792 |
| rs566188891 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081390 | AGGTGATTTAGAGTA[C/T]GGGCTCTGGATTGGT | 114792 |
| rs566204559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075741 | GTAGTCACATAATAC[C/T]TTGATTTATAACTCA | 114792 |
| rs566214255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005543 | GAGTTGGTTGCTGTT[C/G]TTTTCCTATTTCTTC | 114792 |
| rs566227188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089241 | GCAGAAACAAGAAGG[A/G]TATTTAAAAATGAAA | 114792 |
| rs566248853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040694 | CCCGAATCTCATCTT[A/T]AATTGTAATCCCCAT | 114792 |
| rs566259524 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968402 | AAAACAAAAAAAAAA[A/C]CATCTAGCCCAAAAT | 114792 |
| rs566266225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068416 | CTAGACAGCAGGTGG[C/T]AGTGTGAATCCACCA | 114792 |
| rs566292180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081852 | GTGTTGCCAATTCCT[A/G]CTGTAGTCCTGGCAC | 114792 |
| rs566293557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917014 | GAGTCAAAAACATAA[C/T]AACAACCTTAGGAGA | 114792 |
| rs566295418 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030985 | AGAAAAGGAGATATG[A/G]CACCTGCCTTCATGG | 114792 |
| rs566297787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961009 | TGTAAGTCAGTTGTC[C/T]CCTGGATCAGGAAAA | 114792 |
| rs566308395 | snp | C/T | 0.197082 | 0.244335 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901897 | AGCTCCATCCATGTC[C/T]CTGCAAAGGACATGA | 114792 |
| rs566328830 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987118 | CTTCTTTATTAGTCT[G/T]GCTAGCGGTCTATCA | 114792 |
| rs566354313 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096729 | ACTCCTGTTTGAGGC[A/G]TGCCCTCTGATGGAT | 114792 |
| rs566359884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978287 | TTTTCAATTTTCTCC[A/C]TTCCCCCAACCTCCA | 114792 |
| rs566376932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901407 | AGCCAGCAGTTGCAT[C/T]ACTTCATTGTCACAT | 114792 |
| rs566391233 | snp | A/G | 1.64849e-05 | 0.00287092 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132729 | AATTTGGACAAATGA[A/G]CCTCTGGCTTGTATC | 114792 |
| rs566394890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938988 | TTCTTCCCAGGATTA[A/C]TGCTCTATGGATGTA | 114792 |
| rs566410489 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089975 | TATTCTATTAGGTTG[A/G]TGCAAAAGTAATTGC | 114792 |
| rs566419990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011100 | GGGAGGAGGGACAGC[A/G]TTTGGACATGAGGGA | 114792 |
| rs566420797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105002 | ATTATTTCACCTTAC[A/G]TGATTCACGTTAAAG | 114792 |
| rs566443926 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061850 | GCCAAACACAAATTC[C/T]CTGGAAAAATATATT | 114792 |
| rs566455563 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128779 | CTTTGCCTTTGCAGC[A/G]GTTGGTGGCTCACCT | 114792 |
| rs566459016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992934 | CTGTGTGCTCTGCTG[A/G]ATTCATGTGCATTTC | 114792 |
| rs566473090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082379 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 114792 |
| rs566483690 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105672 | GAATAAAGGCTATGA[G/T]CAAAAAGACCAGTCA | 114792 |
| rs566483758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097667 | AAATGGAGCTCAAAG[A/G]CACAACACATCTAGA | 114792 |
| rs566506883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034130 | GAGCTTTTCCCCTAC[A/G]TTTTCTTCTGTATTG | 114792 |
| rs566512594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125961 | GAGAAAGAAGTTATG[A/T]TTACAAGTTTTCTAA | 114792 |
| rs566514611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111042 | TCTTGGGGGGGGGGG[A/G]TCTTAGCCAACCACC | 114792 |
| rs566543201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098497 | TCATAATTATTGTAA[C/T]TTTACTTCAAGTGTT | 114792 |
| rs566551369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000911 | TGAATTTATATTACA[A/G]AGTGAATGAAGCCAG | 114792 |
| rs566559771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934138 | GCGTCAGAAAATCAT[A/G]TATTTACCACTGTCC | 114792 |
| rs566572875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126691 | AGATGCGTTGTGTCA[A/G]ATATACACTGGCTTT | 114792 |
| rs566581686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96969454 | CTGTTGCTAAACCCT[C/T]AAGTTCTCTCATTTC | 114792 |
| rs566587138 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907028 | AAAAAGATAATTCAT[G/T]TACCTAGCTAGCTGC | 114792 |
| rs566610007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015837 | TATGGTTTCATGGGT[C/T]GGCCCGTCACTATGT | 114792 |
| rs566623206 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975427 | TTTAATAATAAGCTT[C/T]TCTGGTTTAATTGCC | 114792 |
| rs566627745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118781 | AGCTCAAGTTCCTAA[C/G]CTCTCCAAGTCCTGT | 114792 |
| rs566642849 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019912 | AGCCTCCCAAGTAGC[A/T]GGAACTACAGGCGCC | 114792 |
| rs566663027 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916853 | ACGTTTATAGTGCTA[C/T]TTTTTTGGTGCTCAT | 114792 |
| rs566668919 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018246 | GATGACAGATATTAG[A/C]CCAAATATTTTAGTA | 114792 |
| rs566672792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994665 | ATGAATGATTAGTTG[C/G]GTGCAAAGTACTATG | 114792 |
| rs566680058 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044079 | GTTTCTGATCTTAAA[A/G]GAGGAGCTTTCAACT | 114792 |
| rs566690106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111456 | CAGAGGTAAACTTCA[A/C]TCACTCGAACCCGCT | 114792 |
| rs566697364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127564 | ACACACACAGATATG[C/G]ATCTTTAGCTTATAT | 114792 |
| rs566711526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96926464 | TAATCCTCACAACAA[C/G]CCTTTGAGGCCAATA | 114792 |
| rs566717362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062045 | TTTTAGAAAAACTTA[C/T]GTTATAATGAGTGGA | 114792 |
| rs566725997 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918291 | AAAATTTGGGGAATT[A/C]AGGGATGCTAGTTTC | 114792 |
| rs566736518 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056354 | TCGTGATCCTCCCGC[C/T]TTGGCCTCCCAAAGT | 114792 |
| rs566740625 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97143106 | AAATCATAACCAAAT[A/C]CAAATGCCTAATAAA | 114792 |
| rs566743865 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023676 | AAGTCCCAAAGACTT[A/G]TCACCCAGCAGGCTT | 114792 |
| rs566750713 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001419 | TTGTTTTATTGTTTT[C/T]GAGAAAGGTGGCCTT | 114792 |
| rs566753710 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014314 | AAAAAAAAAAAAGTT[C/T]CTTTTTTCGTATCTG | 114792 |
| rs566758112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119520 | TTAATTGGGAAAATT[A/G]TAGTGAAAGCAGTTT | 114792 |
| rs566764306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128221 | CTGGCCACCAAATCT[A/G]TGTCCCTAGTGGACT | 114792 |
| rs566773502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090760 | TTCTCCTGTAGTACA[A/C]AAGGGAAAACTGAGG | 114792 |
| rs566777246 | snp | C/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005017 | ATTTAGGGAAGAGTA[C/G/T]ATCCTCCCCAATGTT | 114792 |
| rs566779922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056223 | CCATTCTCCTGCCTC[A/G]GCCTCCCTAGTAGCT | 114792 |
| rs566787528 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919159 | CTTTACAAAAAGCTT[G/T]CATATTCAGGTTTTC | 114792 |
| rs566803288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021884 | TCAATTAATGGCAAC[G/T]GTCCAGTTAATGCAG | 114792 |
| rs566812393 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963035 | TATGCCTGTTGTAGG[A/G]GAGGGGGAAAAATCT | 114792 |
| rs566814994 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999329 | TGAGCCTGGGAAGTC[A/G]AGGCTGCAGTGAGGC | 114792 |
| rs566829476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956113 | TTGTGCTGGGAATCT[C/T]CCCTTTTTAAAACCA | 114792 |
| rs566831761 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119399 | AGGAGGAGGCAGAGA[A/G]TGTGACAAGAGAGAT | 114792 |
| rs566853049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904041 | TCCTACCCATCAGTT[A/G]GAAAACATAATGACC | 114792 |
| rs566854557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049494 | TAAAACTCATGAATC[A/G]TTTATTTCTAGAATT | 114792 |
| rs566900462 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116067 | GTGCCTCAGTTATTG[A/C/G]CAATTCACTGAGTTT | 114792 |
| rs566933334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016100 | CCTCATGGAGAACCT[C/G]TGCTAGGGCAATGCA | 114792 |
| rs566948435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947423 | AAGACACAACCACAT[A/G]TTAGGAACATCGATA | 114792 |
| rs566961840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084266 | GAAATAGCCCACTCT[C/T]ATTCTACTTGACATA | 114792 |
| rs566962283 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119223 | CTCAGCACATCACGC[A/G]CAGTGGCACTCTCAG | 114792 |
| rs566974307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921180 | TAATTATGTAATTAC[A/G]ATATTCTTTCTTACA | 114792 |
| rs567000875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083382 | GCGACAGAGCAAGAC[G/T]CCGTCTCAAAAAAAA | 114792 |
| rs567022713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976570 | GTATATGTATTGTTT[C/T]GGATATATATATATA | 114792 |
| rs567035856 | in-del | -/TGT | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007639 | CAGTCTTCAGGTTGC[-/TGT]CCTTTGGATGAGGTT | 114792 |
| rs567036605 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913412 | TTAAATGGATACATA[C/G]CCAGTGGTTTGCTGG | 114792 |
| rs567039623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988855 | AAACTGTTGCAAGGA[C/G]AAAAAACCAAACACC | 114792 |
| rs567042812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050967 | GAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCA | 114792 |
| rs567060195 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974703 | TTTGGTTAATTTTAA[G/T]ATGGTGATTTGTACC | 114792 |
| rs567071063 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940698 | GTTACAGAAAACAGG[A/C]AAATGAACAGTTTCT | 114792 |
| rs567077327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077522 | ATAGAAAACAAGGAG[A/T]CCCAAGATTCACTGT | 114792 |
| rs567085302 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124173 | CAAAGGGGAAGGCAA[C/G]AGAACCAGTTTCCAA | 114792 |
| rs567108194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051562 | GCTACATATTTCATA[A/G]TCCATGGTGTGCATC | 114792 |
| rs567141579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934606 | TCTTTACTACTGAAA[C/T]AGAGGTTATCATTTT | 114792 |
| rs567148972 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896556 | TAGAATTCTGGTAAA[C/T]ATCCAGTGAACCAAG | 114792 |
| rs567153039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913972 | GAGAGGTTATCCTGG[A/G]TTATCCAGGGGACTC | 114792 |
| rs567157518 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941510 | GTGACTTACATTTTA[A/G]TCAAATGAAATGATA | 114792 |
| rs567169144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044496 | CTTTGTCTGGCTTTG[C/G]TATCAGAATAATGCT | 114792 |
| rs567178201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928067 | AACTGTTACCTAATG[C/T]AGGTTATAGACATGT | 114792 |
| rs567180581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113526 | ACTGTTCACCCCAAA[A/T]GGTATCTGAAGCCCC | 114792 |
| rs567199558 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949557 | TTTTTGTAAAAATTG[C/T]GAATATTTTCCATTT | 114792 |
| rs567221020 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112768 | TTTTTTTAATTTTAA[A/T]AAAAAAAAGGAGAAT | 114792 |
| rs567227719 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095529 | TCTCGTCTTCATGCT[C/G]TGTGAAACAGCTGGG | 114792 |
| rs567236682 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042901 | GGGGTCATGTTGATT[A/G]ATTCTTCGTGAAAAG | 114792 |
| rs567247833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063820 | GGAAATGGGTTAGAA[C/T]GGAGGGCTGGGGCAT | 114792 |
| rs567279954 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976387 | TCCAATGTAGAACAG[A/G]CCTCCCTTGGCATCT | 114792 |
| rs567282059 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949121 | TATCCAGTGTTTTCT[C/T]GTTTGTCTATTTACT | 114792 |
| rs567285046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009402 | TAATCTTTTAAACAC[A/T]TTGGCTCTCTGGGCA | 114792 |
| rs567286877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930674 | AGCAGAGCTACCCTC[A/G]TTATGCTATGGAGCT | 114792 |
| rs567287587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950266 | CTCTAAACAAGAACA[A/G]TGTCTAAACAATACA | 114792 |
| rs567294861 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084497 | AGGCTGAGAAAAAAA[C/G]AAAGAACAATTACAA | 114792 |
| rs567300376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972320 | GTATGGTACATCTCA[A/G]TTTGGACTGGCCATA | 114792 |
| rs567311763 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057308 | CCTGCCTCAGCCTCC[C/T]GTGTAGCTGGGACTA | 114792 |
| rs567343069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951773 | CTTTTATTTTTACCA[A/G]TGTTATATAAAGAGT | 114792 |
| rs567363188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099416 | AATCTGATAAAGAAT[A/G]TTTCAGACCTGTGAT | 114792 |
| rs567373013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965202 | TACAGCTATTAATAC[A/G]TAGTATTCCATGGTA | 114792 |
| rs567388580 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958282 | TAGAGTGCTGATTAT[C/G]CTGTGAGTGGGGATC | 114792 |
| rs567405537 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957275 | ATAAATTTGGGAACT[C/G]TAAATCTCATATTTT | 114792 |
| rs567424441 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100019 | GCGCGGTGGTGCACA[C/T]CTGTAATCCCAGCTA | 114792 |
| rs567437848 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96906204 | AAACAGGGAACCCAG[A/T]TAAGCCTGCTTTGGA | 114792 |
| rs567484672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061271 | ACCCAAGCAGGTGAG[C/T]GTCACTGGGGGTAGA | 114792 |
| rs567488594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092714 | CTTCTAATCTATATG[C/T]GGCTAACTCCTCTGT | 114792 |
| rs567493299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098212 | AATGAGCTTTGTACC[A/G]CTTTCATGCATACCC | 114792 |
| rs567495407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086432 | GAATTAAAGAGCTGC[A/G]GCGTCCTGAAGGCCT | 114792 |
| rs567501082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137135 | AGCCAAAACCCCACC[A/G]GGGTTTTCCCTTTTC | 114792 |
| rs567508908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974439 | TGCTTCTGAATGTGG[A/T]TTTTAATTACTGATT | 114792 |
| rs567534273 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085623 | ACATCTGAGTCAAGG[A/G]ATGTTTTTTTCCTGA | 114792 |
| rs567550223 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924454 | GCGGGCGCGCGCTGG[C/T]AGCTCGCCGACGGCG | 114792 |
| rs567558024 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042083 | AAATCCTAATACATT[A/G]ATGACCAAAGTTGTT | 114792 |
| rs567559447 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019075 | AAATCAGAAATCTGT[A/G]ACAAAATTGATAATC | 114792 |
| rs567562603 | in-del | -/T | 0.262435 | 0.249691 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024401 | GGTTTTTGTTGTTGC[-/T]TTTTTTTTTTTTTCA | 114792 |
| rs567568960 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037004 | TTCTAAAAAATGTTC[A/G]ATTTTTAAAATTTAT | 114792 |
| rs567577527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129175 | TAAAAGAGCTAGTCT[A/G]TATGCCTATTAGTGA | 114792 |
| rs567596369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031297 | CTTTTTTAATCTTTA[A/G]ATTAGTTCTAGTTTT | 114792 |
| rs567612404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996429 | ATTTTATAATCCTAC[C/T]TTCTAGTTGCTATTT | 114792 |
| rs567614431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989638 | CTCCTGAATTTGAAT[A/G]TTCACCTCTCTAATG | 114792 |
| rs567616522 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059552 | ATCCTTACCTGAACT[A/G]TGTTTTTCTTTCTTA | 114792 |
| rs567620057 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898046 | GCTTCCGGCGGGAGG[C/T]GGCGGGGCTTAAGTC | 114792 |
| rs567631784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967452 | ATAGATGTGTATATA[G/T]AGAGAGATGTGTATA | 114792 |
| rs567636982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129667 | TGGGTGGATCACCTG[A/C]GGTCAGGAGTTTGTG | 114792 |
| rs567644122 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936699 | ACAGCAGCCAAAAAT[G/T]TTGTTTTAAAACCTG | 114792 |
| rs567650077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990241 | TTTCACAGTTACAAT[C/T]TGAGTACATTCAGTT | 114792 |
| rs567652981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936020 | TTGGGCCTTTTCTCA[C/G]CTCAGCCTGTCCCTT | 114792 |
| rs567735474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095416 | TCTCATGTAAGTTTT[A/G]GGCAATGTAGAGGGG | 114792 |
| rs567744143 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114620 | AAGATTGAACCAAGC[A/T]TGCCATTTTAGCTAA | 114792 |
| rs567765547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061320 | TTGGCTTCTTTTAGG[A/G]TTTCCTTTCCCCCCA | 114792 |
| rs567776893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998099 | TATTCCTAGCCTGCT[C/G]CTCAACCTCCATTGA | 114792 |
| rs567797059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088209 | TAAAATATATTGTTT[G/T]TTTAAAATTTAGTTC | 114792 |
| rs567801528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013532 | AGTCACCCTGCTCTC[C/T]CCACCACATACATAC | 114792 |
| rs567805946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108054 | GACCTCCTGTTGTAC[A/G]TGGAAATGACGGTCT | 114792 |
| rs567824824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97059544 | GTTTTATTATCCTTA[C/T]CTGAACTATGTTTTT | 114792 |
| rs567827252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017370 | CCAATGTTTTGGCTA[A/C]CATAGGGAATGCCCT | 114792 |
| rs567848547 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058767 | GGTGGTATGGCAGCC[A/G]ATTTGAGACCATGAA | 114792 |
| rs567853450 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011264 | CTTCTTTGAATCCTG[A/C]AAGAGGTGGTTGCTG | 114792 |
| rs567870199 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028167 | GTTCACCTGGGGCTT[G/T]CGTTAAAACTCAGCT | 114792 |
| rs567885570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930963 | TAGAATTAATAGTGG[C/T]AGCATCAAGTACCTG | 114792 |
| rs567919474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959554 | CTTAGAAGGATGCCA[A/G]TCATTTTGAATTAGA | 114792 |
| rs567926733 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922233 | CAGGCTAAAACAACT[A/G]GAAGCTGCAGACTAC | 114792 |
| rs567950085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124744 | TGTAGGCAAGCTGGA[C/T]GTTAATCTGGTGGTT | 114792 |
| rs567957162 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914988 | AGGCACGGACCATTG[C/T]GCCCGGCAATCCTGG | 114792 |
| rs567971192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915811 | CCACTTTGGCATAAG[A/G]ATTATTTTGAGCTTA | 114792 |
| rs567988549 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986999 | GGAGCTGTTCCTATG[C/T]GGCCATCTTGGCTCC | 114792 |
| rs567992618 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127970 | TTTTGTCTACATTTC[A/G]TGTACACCCAATTAC | 114792 |
| rs567994632 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018789 | AAAGTAACAATCTAT[C/G]AGATGACAGTTATGA | 114792 |
| rs568003736 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102871 | AGGTTTGGGAGTACA[C/T]GTGAAGGTTTCTTAT | 114792 |
| rs568009131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117404 | TCTGTTCTCTAGAAC[A/G]CAGAATGAATGTTTC | 114792 |
| rs568028576 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978237 | TACAGATTATTTCAT[C/G]ACCCAGGTAATAAGC | 114792 |
| rs568046623 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899434 | ATTTTAAAAGTGAAA[A/G]TCTCATTTTCATAGA | 114792 |
| rs568048078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046164 | TGACATTTCCTGGAG[C/T]ACCTTCTGAAAAAGC | 114792 |
| rs568070022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005113 | ATCTGTCTGGTCCTG[A/G]GCTTTTTCTGGTTGG | 114792 |
| rs568073272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131754 | GCTGCTGGGGGAGGC[A/G]ACGCTGGGAATCTAA | 114792 |
| rs568081850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019261 | CCTTTTTGCAATTTG[A/C]GTTCCTTGGGAAGTA | 114792 |
| rs568086204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960179 | TTATCATCTTCATCA[C/T]TATCATCATTGTCAT | 114792 |
| rs568107688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081050 | ATGGTGAGGCCAACA[A/G]ATCAGGAGACAATTA | 114792 |
| rs568123352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952042 | CACATCCTAAAAATG[C/T]GCACATTCGGTTCAC | 114792 |
| rs568141447 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943545 | GATTCCTCCACATTT[C/T]GTATGAGAAAGCAGA | 114792 |
| rs568151258 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900391 | AAAGTGATAAAAAAA[A/T]TTGAGATTACGGTAA | 114792 |
| rs568170184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039718 | CCAGCTACTCGGGAA[A/G]CTGAGGTAGGAGAAT | 114792 |
| rs568181332 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984397 | GATGTCTATTAGGTC[C/T]GCTTGGTGCAGAGCT | 114792 |
| rs568203922 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97026163 | AAAAGGTGTTTGAAA[A/G]CTTGTGGATGATTCC | 114792 |
| rs568206889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013834 | CTTGCTGTGACTTAT[C/T]ATATTGGGTTATTTC | 114792 |
| rs568225280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918139 | AGAAGTAAATAAAAA[C/T]GGAAAGAGCTGCTGT | 114792 |
| rs568226625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944183 | CTGATCATGCTGACA[C/G]CAGTAATATTAACTG | 114792 |
| rs568227233 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910233 | CCTCCCTGTTTTTAA[A/T]AACCCCATCCCCAGG | 114792 |
| rs568228417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982787 | GATTTTGGGCTGAGA[C/T]GATGGGGTTTTCTAG | 114792 |
| rs568259906 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955210 | TTTTGGGGGAGACAC[A/T]TTCAGTCCACAGCAT | 114792 |
| rs568262176 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975356 | TTTCAGCTTTAAATT[G/T]GTTTTCATTTACAAT | 114792 |
| rs568265472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938234 | TGTCTCTGGCCACCA[A/G]AGTAGTGAAGTTATA | 114792 |
| rs568274578 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016931 | TCCTGCTGCCATGTG[A/C]AGAAGTCCTTGCTTC | 114792 |
| rs568287576 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924985 | CCGGTGCCTGCGCTG[C/G]CGTCTCTGGCACCTA | 114792 |
| rs568288489 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911111 | AGTACCACAAACTGG[A/G]GGGTTTAAACAACAG | 114792 |
| rs568299462 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141629 | CACTATAGTAATTCA[A/T]CTTCCATTTCCATTT | 114792 |
| rs568315473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075145 | TAACCTAATTGTAGA[A/G]TTCCTCTGTTACACA | 114792 |
| rs568345329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983232 | CCAGGGATGAAGCCC[A/G]CTTGATCATGGTGGA | 114792 |
| rs568352010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938796 | ACAGTTACACCCACC[C/T]TGCAGTATAATCATG | 114792 |
| rs568365398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976386 | CTCCAATGTAGAACA[G/T]ACCTCCCTTGGCATC | 114792 |
| rs568367646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932782 | CACTATGTTTCCCTG[C/G]CTGGTCTCGAGCTCC | 114792 |
| rs568384574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103421 | GGTTTCACCATGTTA[A/G]CCAGGATGGTCTCGA | 114792 |
| rs568389981 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952639 | TAATGAAAGGCCACA[A/G]GATTAGGATTGTGAG | 114792 |
| rs568395446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946337 | CAGTTTTTTAAAGCA[C/G]TTATTATCTCGTGGC | 114792 |
| rs568397057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067666 | CCTTAACACTGGTGG[A/G]TGTTGTTTTCTTTTT | 114792 |
| rs568423994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041991 | AAAAATTTATGTCCA[A/G]CGTCTTGGTACCATG | 114792 |
| rs568452373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976891 | GACACACACCACCGC[A/G]GCCAGCCTATATATA | 114792 |
| rs568452513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937690 | ATCAGGGGCTCTCAG[C/T]CTCTCCTTCCACTTC | 114792 |
| rs568467099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035027 | TAGGACTTCCAGTAC[A/T]AAGTTGAATAAAAGC | 114792 |
| rs568477982 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961104 | GAGGACTATTTCAAG[A/T]CATAGCAAAGAAGAC | 114792 |
| rs568516250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953362 | TTGCCAAGCTTGTTG[G/T]CTCATGCCTGTAATA | 114792 |
| rs568516693 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939833 | CTGATTACAGGGGAA[C/G]AGTAATCAGAATAGG | 114792 |
| rs568523263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104002 | GCCAAATAACTGATC[C/T]AATGTCAGCCATATA | 114792 |
| rs568532222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901481 | ACCCTTATGATTACA[C/T]TGGACCTGCGTGGAT | 114792 |
| rs568564325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055720 | AAAGAATTGCTTGAA[A/C]CTGGGAGGTGGAGGT | 114792 |
| rs568565788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069160 | AAAGCCCAAATTCTT[A/T]CTATTCTTCACTCAG | 114792 |
| rs568579266 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123769 | GCATGGAATCTATCT[C/T]TGCAAGTGCTTTGAT | 114792 |
| rs568616014 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97096870 | TTACAGGATATTCCT[C/G]CCCTTGGTTTTATCT | 114792 |
| rs568623071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97048541 | TTCATTCAGTCAGAG[A/G]TCTCACCATAGTAAC | 114792 |
| rs568629268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082388 | GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTGAG | 114792 |
| rs568642493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126181 | TTAGCTGCTTCTTTG[C/T]GATACTGATTAAAAT | 114792 |
| rs568646637 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069685 | TATGTACTGAGGGAT[C/T]GAAAGGTGCCTCCAT | 114792 |
| rs568653531 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000009 | GAATGTCTGTGATCA[C/G]AACCTAAAGGATGCT | 114792 |
| rs568656035 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065011 | TGCACAGGGTTCCCT[G/T]CAGGAGCCGGGGGAG | 114792 |
| rs568679625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953984 | AAAGTCTCTCTGGAT[C/G]TTTCTGAACTCCTCT | 114792 |
| rs568708869 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970696 | GGAAACAAAACTATT[A/C]ATTCATAATTAAGTT | 114792 |
| rs568720136 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993080 | GTGCTAAGTGCTGGA[G/T]TTTTGGTATTTAAGA | 114792 |
| rs568720475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902009 | AGGTTGATTCCATGT[C/T]TTTGCTATTGTGAAT | 114792 |
| rs568727564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947230 | ACCTAACTGTAGCCA[A/G]TCAAGTAATTTCTTA | 114792 |
| rs568739160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971525 | CTTTCCTGAGACCTC[A/G]TTTATTTATTTCCCC | 114792 |
| rs568744252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134419 | AACAAACTTTTCTCT[C/T]AAAGAGTGCTTCTAG | 114792 |
| rs568747255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983911 | CTTACTTATTTCTTG[C/T]CTTCTGCTAGCTTTT | 114792 |
| rs568765143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082552 | CGGGAGGCGGAGCTT[C/G]CACTGAGCCAAGATA | 114792 |
| rs568804007 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126893 | TTGCATATGTGGCTT[G/T]CATATGTGGCTCTTG | 114792 |
| rs568809256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993697 | GCTACCACACTGTTA[C/T]AGATGCTGGTAGAAG | 114792 |
| rs568809269 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987575 | TCAAGCTACCAATGA[C/T]TTTCTTCACAGAATT | 114792 |
| rs568824071 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934673 | CTGCAGAGAGCAGCT[A/T]ATATCCTCATAGTTG | 114792 |
| rs568825969 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071130 | TTACCGCAGCTGCTC[C/T]TTGCCCTCACTACCC | 114792 |
| rs568826461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97076628 | CTATGAAATTAGGAA[C/T]CTAAGTAAATATGCA | 114792 |
| rs568827161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964247 | GGGTTAATCCATGTG[C/T]GAGGCATGGGAAAAA | 114792 |
| rs568845655 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988019 | AAGAAAACTTAGGCA[A/T]TACCATTCAGGACAT | 114792 |
| rs568873476 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028376 | TCTTACACACACCCA[A/G]CACAGCTTTGAAAAC | 114792 |
| rs568877332 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103395 | ATTTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 114792 |
| rs568908171 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118842 | ATATAGTAGAGGGAA[A/C]AGACTTTTAAACAGG | 114792 |
| rs568909402 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984289 | TTTGCTGAGGAGTGC[A/T]TTACTTCCAACTAAG | 114792 |
| rs568911364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020769 | AAACATTTTCTTCAC[C/T]TGACTTTGTTCCACA | 114792 |
| rs568914775 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946694 | TTGTAATTTTCATCT[G/T]ATGTTTTTGCCATTT | 114792 |
| rs568915156 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97083532 | TGCCTGCCTTGGTTG[A/C]CTCCAGGTGCCTGTG | 114792 |
| rs568916881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105105 | TTTAAAGAAACTGTA[G/T]GTAATATTAAAAGGA | 114792 |
| rs568916974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092107 | TGATTCTCCAGCCTC[C/T]GCCTCCCAAGTAGCT | 114792 |
| rs568927969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909668 | AACTCAGGTATACTG[A/G]TTTCCCATCCAGTGC | 114792 |
| rs568954236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927172 | CTGGTGAAACAAAAG[C/T]ATATATAGTTTAGAA | 114792 |
| rs568956385 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056252 | CTGGGACTACAGGCG[C/T]CCGCCACCACGCCCG | 114792 |
| rs568961865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988905 | TGGGAATTGAACAAT[A/G]AGAACACATGGAGAC | 114792 |
| rs568967400 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119405 | AGGCAGAGAGTGTGA[A/C]AAGAGAGATGGATAA | 114792 |
| rs568976154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084538 | TTAGGTGGATTCAAT[A/G]TAGAATTATTCAAAC | 114792 |
| rs569030667 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111947 | CCAACTATAGTCTCT[A/G]ACATTTAGCTGCTGC | 114792 |
| rs569036626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014654 | ACTGTCCATGCAACA[C/G]TTCTCTGAGGCAGGT | 114792 |
| rs569047668 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976681 | TTGGCTCACTGCAAC[C/T]TCTGCTTCCTGGGTT | 114792 |
| rs569047669 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000653 | GACATCAAATAAAAC[A/T]TGCAAGAATGGGTAT | 114792 |
| rs569047863 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025950 | TTCTCATTATCACAC[C/T]AGAGCTATAGGGAGG | 114792 |
| rs569049480 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989078 | CCTGCACGTTGTGCA[C/G]ATGTACCCTAAAATT | 114792 |
| rs569051886 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918596 | ATCCCACACAAAGTT[A/C/T]TAAGATTAGAAACTA | 114792 |
| rs569054232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105749 | TTCAGTGAAAGACAA[C/T]ATTTGTAGACCAAGA | 114792 |
| rs569066780 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028554 | AAATTTCCTTTTTTC[A/G]TATTTTCTCTGATCC | 114792 |
| rs569073996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007528 | CATTGCTGACAAACT[A/G]GCGTGGCTGGTTGAA | 114792 |
| rs569078368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015539 | TTTTGCCCCTGCCCT[A/G]GAGACCTGTGGAACT | 114792 |
| rs569102521 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047852 | TATAAAAAGAAGAGC[C/G]CTGCTTGGAAAGTAG | 114792 |
| rs569103527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099332 | CTGGGCCTGCTCATG[A/G]GGCCCAGTTTCTTTT | 114792 |
| rs569108776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919255 | TTCCAGTAATGAGGT[A/T]ATCAATAATCAATTT | 114792 |
| rs569109297 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004263 | GACTGAGTTCTTGAT[C/T]TGGCTTTCAGCTTGG | 114792 |
| rs569117556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97098662 | TGTTTTAATGCAGCC[C/T]TTATTTAATGAACAG | 114792 |
| rs569140729 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135378 | TGGCGTGATCTTGGC[C/T]CACTGCAACTTCTGC | 114792 |
| rs569140887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121096 | GTCTTAACTGTATCC[C/T]GAATAAGTTGCACTT | 114792 |
| rs569158568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001320 | GTTTTACTGGTGAAC[C/T]TAAAACTGGTCTAAA | 114792 |
| rs569160147 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007957 | GTGGAATTTGTGCTC[A/G]CTTGCACATGCCAGC | 114792 |
| rs569172729 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912041 | TATAGAGATGTCTTC[A/C]CAGAAGTCCTACAGG | 114792 |
| rs569183188 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018550 | AGGTTGCAGCGAGCC[A/G]AGATCACACCACTGT | 114792 |
| rs569184057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016157 | CACACAGAGTCCCCA[A/C]TGGGGCACTGCCTAG | 114792 |
| rs569185881 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956342 | AAATGTAGTAACTTC[A/T]TGAAGGTCACATAAG | 114792 |
| rs569186326 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912632 | ATTTGCTCCATGAAT[G/T]TTACAAAAACCAAAT | 114792 |
| rs569197770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956863 | TTTCTTGCAGATGTA[A/G]GAAGCACATCAGGTT | 114792 |
| rs569222892 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984192 | TAGTTGAGCAGTTTC[A/G]AGTCAGTTTCTTAAT | 114792 |
| rs569249344 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994683 | GCAAAGTACTATGAG[G/T]TCCTGTGATCATCAC | 114792 |
| rs569260799 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043106 | CCTCACCAGAAGCAG[A/G]TGCTGGAGCTATGTT | 114792 |
| rs569274203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016537 | CCATTTTATCTAGGA[A/G]GTAACTAACTTGCTT | 114792 |
| rs569300795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035791 | TTTTGAAATTTAATT[A/G]TAATGTATCCTGGTG | 114792 |
| rs569315878 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009459 | TTTAGGATTTACTGG[A/C]CATGCTGTTGCTTCT | 114792 |
| rs569322253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128893 | GTGGCAGGGGACTGG[A/G]CTGCTAATGCAAACA | 114792 |
| rs569334174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107715 | GCCTTGAGGGCTTAT[A/G]AAGGCCTTATAAGAA | 114792 |
| rs569342740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128293 | CTGTATTTAATGAAG[A/G]CATTTCTCTCTTTGC | 114792 |
| rs569360629 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905030 | TGTCCTCATGAACTT[G/T]CTTTATATGGAAGTA | 114792 |
| rs569365249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078192 | TGGGAGTGGTTTTAA[A/G]AAGAGAATTTCTTGA | 114792 |
| rs569369894 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958818 | GGTAGCTGGGTAGAA[A/G]GAGTGCCAAGGAAAA | 114792 |
| rs569383873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029952 | TAAGATGTAATGGAT[C/G]TACTGTAATCATTGC | 114792 |
| rs569392193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030414 | AGGGAATAACACACC[A/G]TAAATCCACACCTCC | 114792 |
| rs569393756 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122771 | ATGTATCATCATCAC[C/T]GTTTTGCATATGAGG | 114792 |
| rs569407194 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913996 | GGGACTCAACGTAAT[A/G]AGAACCGTCCTTAAA | 114792 |
| rs569414458 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119750 | AGTCTGGCTTCCTGT[A/G]TACATTTAGGGAGAG | 114792 |
| rs569419932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914847 | CCTGGTGGTTCCCTG[C/T]TCCCGGGAGGTGACC | 114792 |
| rs569436803 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952050 | AAAAATGTGCACATT[C/T]GGTTCACTGGTGTGT | 114792 |
| rs569441710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941579 | TGATATGATGTGATG[A/T]CCAAAAAACAATCAA | 114792 |
| rs569462506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980556 | TGTGCTTCTGGATTT[A/G]ATTTGCTAGTATTTT | 114792 |
| rs569470723 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929176 | AATAAAATAGAAGGC[A/G]TCATAGCTAGAGTCT | 114792 |
| rs569471882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022550 | TCTCAACTCACTGCA[A/G]TCTCCGTCTCCCAGG | 114792 |
| rs569476836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933792 | GCCTTTTCTTTAGGC[A/G]GCAGTCACTCATGGT | 114792 |
| rs569478402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935161 | ATTTTAAGAGAATTC[A/G]TTTTGTGGTGTGTGA | 114792 |
| rs569524084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063837 | GAGGGCTGGGGCATC[A/G]CTAAAGGCCTCCTTG | 114792 |
| rs569539290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037840 | CATAGATCAATGGAA[C/T]AGAATAGGGAACCCA | 114792 |
| rs569543786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972469 | TATAGCATATACTCT[A/T]TTGTATTGATGCAGT | 114792 |
| rs569548167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973537 | CCATCCCAAAACTTT[C/T]AGTCACAGTATGAAG | 114792 |
| rs569559601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138703 | GACACTGAGCTAGAT[A/G]TCATCAATTTTCACA | 114792 |
| rs569563066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935555 | TCTATCATCAATTGA[C/T]TTTGAACTTGCAGCC | 114792 |
| rs569584862 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921833 | AGCACTAGATTTATG[C/G]TACCCTCCTATATCT | 114792 |
| rs569585743 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064526 | ATTGAAATAGAGTAC[A/G]TAAAGCAGCAATTTA | 114792 |
| rs569586192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96943349 | ACACAAGACCTGTGC[A/G]GTAATATGATATTTA | 114792 |
| rs569627250 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038516 | AGAGGCAATAACAGA[G/T]TCTGGCAATGATATG | 114792 |
| rs569627612 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978831 | TACTTTTTAATCATA[-/G]TCATTCTGACTGGTG | 114792 |
| rs569627652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031362 | TTTTTTTGAGATAGA[A/G]TCTCACTCTTTTGCC | 114792 |
| rs569634125 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014899 | CCCAAATCTCATCTC[A/G]AATTTTAATCCCCAT | 114792 |
| rs569636173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101132 | ATTCTTGAATCAATT[C/G]ATGAACAAATATTCA | 114792 |
| rs569650606 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945692 | CTTAAAATTTTGGTC[A/G]TTGTAGGAAATGGCA | 114792 |
| rs569657452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100151 | TATCTCAAAAAATAC[A/C]TATATAAATATATAT | 114792 |
| rs569666802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032078 | CTCAGAGAAGGTAAC[A/G]AATTAGCCAAAGTTT | 114792 |
| rs569671940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051757 | AAGTTAATCATTTAT[A/G]TAGTGGGGAGTCTTG | 114792 |
| rs569703232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966041 | TATTATATTTCACTC[A/G]GATTGTAAATCATAG | 114792 |
| rs569715266 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045098 | GTGTCTTAGAATAAT[A/T]GAGGCAACTCTGGCA | 114792 |
| rs569721794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937253 | CCCTCTCCATCATAG[A/G]TAACCTCTGCTGTGC | 114792 |
| rs569724729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002843 | AAAAAGAATAGTACA[C/T]ATGTAGTACATATTC | 114792 |
| rs569732698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044526 | TAGTCTCATAAAATG[A/C]ATTTGAAAGTATTCC | 114792 |
| rs569754091 | in-del | -/CTAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031943 | TTATAGCGACAGTTT[-/CTAC]CTATATAACATTTAC | 114792 |
| rs569770449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065985 | AGTAAATGGTTAATG[A/G]TTTTTTTTTACCTTA | 114792 |
| rs569779526 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974898 | GCTTAATCATCCCAA[C/T]GGTATTTTTACTCAG | 114792 |
| rs569782385 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139526 | TGCCAATTTAAGGTA[C/T]ATTGTGTTCCATGGG | 114792 |
| rs569790122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949672 | GATCATATCTTCAGA[A/G]TTCCCTGGTGAGATT | 114792 |
| rs569796996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950434 | CCACGTTCTTTCTTC[C/T]ACCTTACATCTCTTT | 114792 |
| rs569814847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97093794 | TTCCTTCAAAGTACA[C/T]GATGGTGTAGTATAA | 114792 |
| rs569827082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958867 | TGCAGAAGGCATGCA[G/T]GTGCACACACAGCTT | 114792 |
| rs569842988 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142270 | TTCTAAAAGCACAAT[C/T]CACAAATGCAATGAA | 114792 |
| rs569851900 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111427 | CTGGGGCTAGCCAGC[C/T]GCTTCAGTGCCAGCA | 114792 |
| rs569871701 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107677 | TGAATCTAAGTTTAG[A/G]GCACTGTATGCTGCA | 114792 |
| rs569875977 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137157 | TCCCTTTTCTCATGG[A/G]GCGAAGTAGTGATAC | 114792 |
| rs569877993 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129710 | AACATGGTGAAACCC[C/T]GTCTTCACTAAAAAT | 114792 |
| rs569891487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060364 | AGAATTGAGAGAGTG[A/G]ACATCTGATGATCCA | 114792 |
| rs569913509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951158 | TACATGGGTCAGACT[C/T]ACATGGTCTCGGTTT | 114792 |
| rs569922659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123060 | GTTAGCACTGCATTA[C/T]GACCCATAGACATCT | 114792 |
| rs569943194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073303 | TTCTCTTTGATTTTG[C/T]TGAAATGCATACATT | 114792 |
| rs569971825 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916341 | TTAGGTCACAGTTCA[C/T]CCACAAGGGCTCAAA | 114792 |
| rs569977678 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899191 | ATTGGTATTTGGAAT[C/T]TATAGAAGCTGAAAT | 114792 |
| rs569989254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097607 | AAGTTCTTTCACTCG[A/G]TGACCTTCACAGCAG | 114792 |
| rs569991609 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043027 | GTGCTTCCTCTCTTA[C/G]TATGTGATCTTGGCA | 114792 |
| rs570006491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990778 | GCGGGGCTTGCTTGG[C/T]GATGAGCAGGGAGCA | 114792 |
| rs570009527 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920205 | CAAGGAAAATCCTTG[-/GA]GAGAGCAGAGTTGGC | 114792 |
| rs570012732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986147 | GTCCACTCCAGACCC[C/T]GTTTGCCTGGGTATC | 114792 |
| rs570021152 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084888 | ACTCCTTTTATTAAG[A/T]TGTCTTTAAATATAT | 114792 |
| rs570024807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982157 | CAGTGAGGTGTTGAA[A/G]TCTCCCAGTATTATT | 114792 |
| rs570029003 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018121 | TTGATGCAGTCAAAA[A/C]GAGTACAGTAAGTAT | 114792 |
| rs570034688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960275 | GCAGGAAGAGGAGGA[C/G]TAGCATTTTCCCTAT | 114792 |
| rs570073384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960898 | AGACCTAGAATCAAC[A/G]GAAAGGAATGTCTGG | 114792 |
| rs570076144 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959516 | CGGTCTTTCATTTGT[A/G]TTTGCATGTGTTTTA | 114792 |
| rs570115426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089036 | CATAGGGAGAAAGTA[C/T]GGCTCTCCACCCATC | 114792 |
| rs570115739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081242 | AGCAGGGTTAGCAGG[C/G]TTATGATTGGCTAGT | 114792 |
| rs570140094 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100451 | TATCCCCTTGACAGT[A/G]GAGTCTGGCCCTGAC | 114792 |
| rs570158629 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939489 | ATGGCATTGTTAAAA[-/G]TATAAAGTGGGAAGC | 114792 |
| rs570171478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986823 | CCTTGCACTTCCTGG[A/G]TGAGACGATGCCTCG | 114792 |
| rs570174042 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982596 | GAAGAGGTCCTTCAC[A/G]TCCCTTGTAAGTTGG | 114792 |
| rs570177683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97081796 | CTTCCAGTAGACTAT[A/G]TATACCATAAGGCCT | 114792 |
| rs570184548 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087707 | CACACACACACTTAC[A/G]CAGGTGGCTCTTCTA | 114792 |
| rs570198171 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006916 | TCTCTCTAGATGCTT[G/T]TAAGAGTTTTTCTTT | 114792 |
| rs570231793 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976243 | CAATGTTTCCCAAAC[A/T]GTCACTAAACCAGGA | 114792 |
| rs570238787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095565 | CTGTTTTCGACCCCA[C/T]GTGTAGTCAGTATCC | 114792 |
| rs570253380 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986288 | TCTGCCCCTAATGGG[A/G]GGGGCCTCCCAGTTA | 114792 |
| rs570253603 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987066 | TGATATCCCCTTTAT[A/C]ATTTTTTATTGCATC | 114792 |
| rs570262658 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924571 | GGATCGCGGGGGAGG[C/G]GGAGGGAGCGCGCGG | 114792 |
| rs570265097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012732 | GAAAATGTTGAGAAA[C/T]GTAATTCAGTCATAG | 114792 |
| rs570266374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004608 | GTATGTTTGCTGAGG[G/T]TTTGTTGTAGATGGC | 114792 |
| rs570285240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998331 | AATTAGAATCTGCTC[A/G]TTTGATCTGCAGGAA | 114792 |
| rs570296514 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057677 | TTGCAAATATTTTCT[C/G]TTAGCCTATGGCTTG | 114792 |
| rs570296960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983376 | CCAGGCTTTGGTATC[A/G]GGATGATGCTGGCCT | 114792 |
| rs570303182 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014549 | TATGACTTCATAGGC[A/T]CTACTACTGAAGTTT | 114792 |
| rs570317612 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988838 | AAACCATCATTCTCA[A/G]CAAACTGTTGCAAGG | 114792 |
| rs570325124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916516 | GTCTCTTGAAGCTCA[A/C]ACCTATTTTCCTTTG | 114792 |
| rs570339786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110366 | ATTTCTCTCACTCTG[C/T]CACTCATTAAGAGAT | 114792 |
| rs570352044 | in-del | -/CAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051002 | AGCAAAACTCCATCT[-/CAAA]CAAACAAACAAACAA | 114792 |
| rs570356291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97005408 | GTGGTCTATCTCTCT[C/T]ATTTATTCTTTCAAA | 114792 |
| rs570370673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909055 | TCCAGGGATCTAAGC[A/G]GCAGAAGGGCTAAGA | 114792 |
| rs570392629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006048 | GTCAAGTGCTGAGTA[C/T]AGGTCCTGAATATCT | 114792 |
| rs570396921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944397 | AGTTTCTTTACAATA[C/G]ACCTACATAATATGG | 114792 |
| rs570412558 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972649 | TATGGTTCTTGCTTT[C/T]AGTCTTTTTTCCAGA | 114792 |
| rs570432337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910042 | GTTTTGGAGGTGAGC[C/T]AGATTACTGGACTGC | 114792 |
| rs570436280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900416 | CGGTAAGACTCATGT[C/T]CTTCAATAATTTAAT | 114792 |
| rs570440668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97131953 | ATCCTGTGTCAGCCC[A/G]TCAATAAAAAGAGAC | 114792 |
| rs570445967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999208 | CAAGACCAGCCTATG[C/T]GACATAGGGACACCC | 114792 |
| rs570454047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040647 | TGAGAACAACTGAAA[C/T]GGAGTGTGTGATACA | 114792 |
| rs570474191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104141 | TCTTGATTTTCTCTT[C/T]ATCTTGATATAAAAT | 114792 |
| rs570474658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953182 | CATCAGATGATTACA[A/T]ATTTGATTCATTATA | 114792 |
| rs570477066 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954572 | TCTAATTTCCCTGGA[A/T]TATATAAACCTAGCT | 114792 |
| rs570479814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075248 | GAATTGCTGCTAATA[C/T]TTTGTTTTCATTTAA | 114792 |
| rs570480848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992250 | ACCCAGGGTTGCAAA[A/G]GTCCATGGCAGAAGT | 114792 |
| rs570503911 | snp | A/C | 1.6729e-05 | 0.00289209 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132626 | AAATGGATTTTTTTT[A/C]TTTTTATTCAATTCT | 114792 |
| rs570509505 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945271 | ATGCTAACACTGTCT[A/G]TTGCTTACCATGATG | 114792 |
| rs570511885 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97033030 | TTAGCCAGGGAATAC[A/C]TAAAAGAAACTTCAC | 114792 |
| rs570516390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006941 | TTCTTTCATATCTAC[C/G]TTATGGAATCTGAGG | 114792 |
| rs570519658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117493 | GGTCCATTTTGGGGT[C/T]AGGAAATCTTGAAAC | 114792 |
| rs570534005 | in-del | -/TTGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135372 | TGCAGTGGCGTGATC[-/TTGG]TTGGCTCACTGCAAC | 114792 |
| rs570535227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97104886 | AACTGAAACTTTTCA[C/T]TTGGTCTCAAGGAAG | 114792 |
| rs570556455 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962858 | TGCAAACAGCTTCAT[G/T]TTGTAAAATGTGTGT | 114792 |
| rs570565689 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141878 | TACAATGCAATAACA[C/T]TTCTTAGATCCTTAA | 114792 |
| rs570570415 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972491 | TGATGCAGTTCTAGG[A/G]CATCCCTCAGAGAAA | 114792 |
| rs570591802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97125877 | TGGCTCTCTGGACTT[C/T]AAGGAAGATATTATT | 114792 |
| rs570602997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007330 | CCTTAAAGTGAGCTT[C/T]TCAGCTTTACCAGAT | 114792 |
| rs570608139 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008269 | CTGACAGTCAGGTGC[A/G]GTCTGCCAGCAAAGG | 114792 |
| rs570608945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911177 | TCAAGATCCAGCTGC[C/T]AGGATGGCATAGTTC | 114792 |
| rs570610511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925619 | GCAGTTCACTTAGTC[A/G]TGATTATTTTAAATT | 114792 |
| rs570614235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075721 | TTCCTGCAGCACCAG[A/G]TTAGGTAGTCACATA | 114792 |
| rs570621488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902111 | TATACCCAGTAATGG[A/G]ATTGTGGGCTTGGAT | 114792 |
| rs570625192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976986 | GTCAGTACATGCATG[C/T]GGCTAATGAAGACAC | 114792 |
| rs570627616 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142836 | TTAAAAAATGTGTTG[C/T]AAAGCATGGAAGAAA | 114792 |
| rs570630038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938896 | TTTTTGTTGTTGACT[A/G]TTATGATATTCTAAA | 114792 |
| rs570635572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034086 | TTTGGTGTCTTATCC[A/G]AAAAATTATTGCTTA | 114792 |
| rs570639515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000781 | CAAAATGTGAAGCAA[C/G]GAAGATGTTACTCAG | 114792 |
| rs570641388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935494 | TTTGTGAAGGAAAAG[A/G]GGAGGGGTCTGGGAG | 114792 |
| rs570642054 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975561 | TACAAAGGTGGGGAA[A/G]GAATCAGGGAATTAG | 114792 |
| rs570657829 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969691 | AAAACCTGCCTCTGT[A/G]CTTCAAACTTATCTT | 114792 |
| rs570671549 | snp | A/C/T | 6.85942e-05 | 0.00585597 | intron-variant | KLHL32 | GRCh38.p7 | 6:97139084 | ATTTTGAGCAGTCAT[A/C/T]TTTGATACACAAGCT | 114792 |
| rs570683134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902846 | TATTAAATAGGGAAT[C/T]CTTTCCCCCATTGCT | 114792 |
| rs570701811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019791 | TTTTTATACTATTTT[C/T]TTTTTTTGAGACGGA | 114792 |
| rs570702199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932887 | AGTTGCCAATTTTTG[A/G]TTTCTGTGTTTCATG | 114792 |
| rs570729980 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037609 | TAACAATACTATCCA[A/T]AGTAGTTTACAGATT | 114792 |
| rs570754676 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97135254 | ATACTGCGTTTATTC[C/T]TTTGGCTGGCACACT | 114792 |
| rs570756706 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107719 | TGAGGGCTTATAAAG[A/G]CCTTATAAGAAAGCC | 114792 |
| rs570758894 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035139 | TTTGTATATCTATTA[C/T]AAGTTTTTTTCTGTG | 114792 |
| rs570760503 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981562 | TCCTTCAGTTCAGCA[A/T]TGATTTTGGTTATTT | 114792 |
| rs570762775 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913522 | CTTGACTGATGTCAA[C/T]GTGACATTGCCAAAT | 114792 |
| rs570771880 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061477 | TATGCTCCTCCAGAC[G/T]GATGAGTGACTGGAT | 114792 |
| rs570792726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970372 | AGCTGTTAACTTTCT[A/G]TAGACACTCTATAAG | 114792 |
| rs570796940 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035620 | TTGTATACTTGGCAG[G/T]TTTTTTCTTTCAGTA | 114792 |
| rs570804643 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126723 | GAAGACTTAGTATGA[A/C]AAAAAGAATATGAAA | 114792 |
| rs570825948 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915780 | AAAAGGTCAGAATAT[A/G]CCACCCCAAAATATG | 114792 |
| rs570833248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090141 | TTACCTACTGCTTGC[A/C]CTCTATTAATAATAA | 114792 |
| rs570835178 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055771 | CCCCTGCACCCCAGC[C/T]GAGGTAACAGACTGA | 114792 |
| rs570840275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017891 | TGCAGAGCCCCGTGA[G/T]GGAAGGAACCTGGGC | 114792 |
| rs570881821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934218 | GACCTGAGGTTGTTT[C/T]GAAAATATAGATTAC | 114792 |
| rs570885860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029107 | TTACCATAACTTTGG[C/T]TAAGAAACAACTTGA | 114792 |
| rs570927808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049385 | GAGAGCATCTACAAT[A/G]AGGATATGCTGAACA | 114792 |
| rs570965535 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093793 | ATTCCTTCAAAGTAC[A/C]CGATGGTGTAGTATA | 114792 |
| rs570965754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96927912 | AAGCTACTTCCATAT[C/T]GGCTTCACAATGACT | 114792 |
| rs570979284 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056396 | AAACGTGAGCCACCA[C/G]GCCCGGCCCACCAGC | 114792 |
| rs570989387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97042151 | TTTGAGAACTACTCA[A/G]ATAAATCAATTCAAA | 114792 |
| rs571013234 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994576 | AAGAGTAAGAAGGCC[A/G]AAGCTTTGATGGATC | 114792 |
| rs571014555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954980 | AGTCAAAGATCAAGA[C/T]GCTGCCAGATTCAAT | 114792 |
| rs571027128 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928358 | GATACCTAATATTGA[G/T]GAGCTTACTGTAGCT | 114792 |
| rs571027255 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056401 | TGAGCCACCAGGCCC[A/G]GCCCACCAGCCTGCC | 114792 |
| rs571028421 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097126 | AAGGGAGGGAAAAAA[A/C]CCACGCAAATTTAAG | 114792 |
| rs571038039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947868 | GGGATTTAAACCTAG[G/T]CAGTTTGATTACAAA | 114792 |
| rs571057800 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119009 | GCTGCGGGTCCATTG[G/T]CTACTTTCTATTATC | 114792 |
| rs571069639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947286 | TAAGCCTGAAGCTCA[C/T]GCTGCACAGCTGAGT | 114792 |
| rs571081602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988205 | GTGCAATCTACTCAT[C/G]TGATAAAGGGCTAAT | 114792 |
| rs571081753 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913357 | TCACTGTCTTTGAAA[C/T]GTAATGTAGGTCCCA | 114792 |
| rs571109727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939922 | AGGGAGGTGGGAATA[G/T]AGAAGGAGAGAAATT | 114792 |
| rs571127451 | snp | A/G | 3.29891e-05 | 0.00406122 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127474 | CCAGGTAAGAATCAT[A/G]TAAGAACACCTCATT | 114792 |
| rs571151588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050857 | AAAATAAAAAAAATA[A/G]CCAGGTGTGGCGGTG | 114792 |
| rs571159964 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070522 | GGATGTCAGGAAGCG[A/G]CAGCCCAGAGGCACA | 114792 |
| rs571203403 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934386 | CTGCTTCTTATTCCT[A/G]CCTTCCGAGGACCAG | 114792 |
| rs571207837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984366 | ATTCTGTTGATTTGG[A/G]GTGGAGAGTTCTGTA | 114792 |
| rs571212716 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051449 | AATGGCGAGTATCCA[G/T]TAACTCCAAACAGTA | 114792 |
| rs571246017 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984865 | TTGGAGCATTTAGCC[C/T]ATTTACATTTAAGGT | 114792 |
| rs571251620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022302 | ACTGCCCTTCTTGCT[A/G]TTCCCTCAGACAGGC | 114792 |
| rs571256869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97084750 | CCTGCCCTTACGTTA[C/T]CTTTAGTAGAGAAAA | 114792 |
| rs571273694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063780 | CTGCTGGTCCAGAGA[C/T]CAGATTCAGGAAGCA | 114792 |
| rs571290900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112013 | CTGGCTGTGTCAGGG[G/T]TTTTTATGGGTACAG | 114792 |
| rs571317000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015569 | TCTGAATGTGAGAGA[C/G]ATGATGTGAAATTGG | 114792 |
| rs571336001 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96978976 | TTCATGTCTTTTGCC[C/T]CCTTTTTTTATGGTG | 114792 |
| rs571338614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920075 | CAGGGAAAAAAACCC[A/G]ATGAGGAAGAGTGAA | 114792 |
| rs571342375 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927418 | CTCAGAGACATTAAA[C/T]CCCAGCACCCTGGTA | 114792 |
| rs571343306 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078412 | TCTAAGTGAAGTGCA[C/T]CAATAATTGGAAATG | 114792 |
| rs571343372 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051791 | AGTTCCTTAAATTTC[A/T]TAAGAAGATATCAGC | 114792 |
| rs571345278 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094598 | CCTCCTTGTTACGTG[C/T]GGTGGCATGTTGATG | 114792 |
| rs571351805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96949478 | TTTCTTTCCACAGAT[A/G]TAGACTTGCCACCAT | 114792 |
| rs571352263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105800 | CTTTTAGACAATGAC[A/G]TAGGGCTTTATTCTT | 114792 |
| rs571373311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979741 | ATTGAATGTGTACAT[G/T]GCTTTAGGCAGTATG | 114792 |
| rs571383588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920914 | ATTCTTAGAATTGGA[A/G]TTACTGGACCAAAAA | 114792 |
| rs571398871 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97008064 | CTGCACCTCCTCATG[C/T]AGGTGGTTGTGGTGG | 114792 |
| rs571404425 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053101 | ACACACACACACACA[C/T]ACGCACACACATTCT | 114792 |
| rs571414952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964520 | TAGCAGGGCGTGTTG[A/G]CCGGCGCCTGTAGTC | 114792 |
| rs571432288 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084077 | AAACTATGCACCTCA[A/G]TAAGGAGTTCTTGAT | 114792 |
| rs571432998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079436 | TGCCTTGCAAATGTA[A/G]CTACACTTGAATATA | 114792 |
| rs571433117 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099380 | TTCTCTATCTTCAGG[G/T]TTCACCTTGCTCTTC | 114792 |
| rs571447837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912772 | CAGGACTCCTTGCCT[C/G]ACTTGGAAAATCTCA | 114792 |
| rs571490150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980597 | TTTACATTTATGTTC[A/C]TCAAGGATACTGGCC | 114792 |
| rs571490195 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985997 | TTTTTCCCTATCTTT[C/G]TGGATTTATCTACCT | 114792 |
| rs571493666 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056734 | TTCAGTAAATAATTC[A/G]GGCCATATAAAGTTT | 114792 |
| rs571515813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044267 | ATGGTTGTTATCTGT[C/T]ATTCTGTTAATATGG | 114792 |
| rs571521999 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106653 | GGAGGCTGAGACAGG[A/C]GAATCGCTTGAGCCT | 114792 |
| rs571524920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002085 | ACCCAGGAGAGCTGG[C/T]TGTATGCTTCTAGTC | 114792 |
| rs571529051 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96957413 | AATGTTCATTTTGTC[-/AT]ATTATAAAGTAATAT | 114792 |
| rs571561759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995319 | TTTTGATGGGTCAGA[A/G]TAACTTTTTAATTTC | 114792 |
| rs571568941 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905182 | TAATTTGGCACAGGG[A/G]AAAAAAAGTGAAAAG | 114792 |
| rs571578725 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136165 | TTAAATAGTTCTGAG[A/C]TTGTTCTATTAACAT | 114792 |
| rs571578781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981220 | AGTAGGCTTCTTCTT[A/G]CTGATTCAATTTTGG | 114792 |
| rs571595228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002597 | AGCGTAGTACGCTAT[A/G]GGTGTATTTTTATCC | 114792 |
| rs571596801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108015 | TTGTGGTCAGATGAA[G/T]TGGGTCAGGCAGGGT | 114792 |
| rs571598152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036775 | ATGTGAAGCCGTACC[A/G]GGTGCAGGGTGCCAG | 114792 |
| rs571598364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989168 | TGGTTATTATGCAGA[C/G]TTGATTGTGTGGTTG | 114792 |
| rs571606954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989573 | AATCTGACAACTGTG[C/T]GTCTTGGGGATGGTC | 114792 |
| rs571633373 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897025 | TCCGCCTCCCGGGTT[C/T]GAGAGATTCTCCCAC | 114792 |
| rs571634039 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112586 | CGAGTAGCTGGGACT[A/T]CAGGCACGTGCCACC | 114792 |
| rs571643571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128429 | TGCACATGTGGTTAA[A/G]GAGGAAGAAGGTGTT | 114792 |
| rs571647649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136982 | GCTCCACCACTTGCC[C/G]TGTGACCCTGAGAAA | 114792 |
| rs571674610 | in-del | -/T | 0.0799831 | 0.183287 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040311 | TAGCATGGGGTTGTA[-/T]TTTTTTTTTCCTTTT | 114792 |
| rs571678528 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087295 | TATTTTGCCTCAAGT[A/G]TAGTTAAGTTCATCA | 114792 |
| rs571710586 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940147 | TCCATACAACTGTGT[A/G]ATTATGGCAATATTA | 114792 |
| rs571711492 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129149 | ATCACTTCTTTTCTT[G/T]AGTGTATCTTTAAAA | 114792 |
| rs571716536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121862 | CGCCATAGAAATAGG[G/T]AATGGCTGAAGAACT | 114792 |
| rs571733548 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897271 | TAATCATTTGGACTG[C/T]TAGGAAAATACTTTA | 114792 |
| rs571738556 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072195 | GAGACCTTTCAGCCC[C/T]ACCCCCTTAACTTGT | 114792 |
| rs571740151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071476 | GGCACCCTTCCCTTC[G/T]GCTCACTATCACTCT | 114792 |
| rs571755115 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897493 | CGCGGGCGCGGAGGA[C/G]AGTCTCAATGTCACC | 114792 |
| rs571755300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030515 | GGTGGCAGCACATTA[C/T]CAGCCACAAATGAGC | 114792 |
| rs571774924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113686 | AGTTTGTATTATTAC[C/T]TGCCTGGAAGAATAC | 114792 |
| rs571796525 | snp | A/C/T | 0.000131789 | 0.00811661 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897812 | CCCATCTCCTCATAA[A/C/T]ATTATGCGCTCAGGT | 114792 |
| rs571803292 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064574 | CTACATATTAAGCAG[A/C]ATTATATTTTTAAGT | 114792 |
| rs571819667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936671 | TCTTTGCCTCCTATA[G/T]ACTCTTCTCCACACA | 114792 |
| rs571823295 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129894 | TCTCAAATACAAAAC[A/C]AAACAAAACAAAACA | 114792 |
| rs571823697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016592 | AAGGGACTTTCCTTG[C/T]CTTAGATGAGACTTT | 114792 |
| rs571827590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030862 | TATGACACTGTAGGG[C/T]GGTAGGACATCATCT | 114792 |
| rs571835883 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011395 | TTGGAATGAGACAAG[-/T]TTTCTAATAGTGATG | 114792 |
| rs571841272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031174 | TTCACTGTACCAAAT[A/G]GCCAAGTTCTTCCTT | 114792 |
| rs571846206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017153 | GTAAATTAGCATGAC[A/G]TTTTATAGATGTTAA | 114792 |
| rs571856401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974229 | ATGGGACACGGTAAG[C/T]ACTATGTGTTTCTCA | 114792 |
| rs571865398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97031455 | ATCCTCCTGCCTCAC[C/G]GTCTTGAGTAGCTGG | 114792 |
| rs571910327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929369 | TTTCTTAATAAGCAA[G/T]GGGCTTTTTGGTGAC | 114792 |
| rs571910730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929697 | TTCTTTCCCTATTTC[G/T]TATACACATTGCAAT | 114792 |
| rs571918798 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921889 | ATGAAAAAAATGCTG[C/T]AGAAACTTGTGTTCC | 114792 |
| rs571924314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929952 | AGAAGAAATGTCTTT[A/G]GCAGTTTTCATGGAC | 114792 |
| rs571924431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921917 | TCCAAGATGCTTATC[A/G]AAGTATATTAAGAGG | 114792 |
| rs571966578 | snp | C/G | 4.94564e-05 | 0.0049725 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085203 | GTTGGAGAAGGCAGT[C/G]ATCGATTTCTTAGTG | 114792 |
| rs571969108 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086005 | TCATCCCCAGTGACT[A/G]TTCCTTGAAAAATCC | 114792 |
| rs571973895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930407 | CCAGTTACATATCCC[C/T]TCTAACTCTCATTTT | 114792 |
| rs571978923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037085 | ATATATCAAATATAA[C/T]TGAATATATTATATG | 114792 |
| rs572005107 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989941 | TCAGCTCTATCAGAT[C/G]AGTTTGTTTCTTTCT | 114792 |
| rs572083820 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923330 | TCAAAGACGCTTTCA[C/T]ATTCGATTTTCTGAT | 114792 |
| rs572104525 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KLHL32 | GRCh38.p7 | 6:97052650 | CTGCCCAATAAAGGC[C/T]AATATTGCCCACCCT | 114792 |
| rs572107530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936309 | TATTGGAAGGAAACC[C/T]ACCTTATAGTGAAGG | 114792 |
| rs572119051 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077386 | TGAATTCATTTGATA[A/G]TGTCTGATTTTTTTT | 114792 |
| rs572121126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121635 | GTGTTGTAAAGTTTT[A/G]TTTTGTTTTGTTTTT | 114792 |
| rs572123956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122363 | ATGCATGGATTATGT[A/G]TGCTTCTATTCAAGA | 114792 |
| rs572148618 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924029 | CTGAATTAGTAGTAA[A/C]CACAGTAATCACACC | 114792 |
| rs572157642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079233 | TAATTGAGATATTGA[A/G]AGACACCGCAAAGGC | 114792 |
| rs572166959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053150 | TTCCTCTTTTCTCTT[G/T]CTTTGAGTTATTTTT | 114792 |
| rs572168231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942907 | GTAATGTGTAGCAAC[C/G]TGTTCACCTCTCTCT | 114792 |
| rs572184622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986215 | AGCAGATGTTGCTGC[C/T]GGATCGTTCCTCTGG | 114792 |
| rs572188937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114753 | TGGAAATTGTTGGTC[C/T]ATCACAACTGTTTTT | 114792 |
| rs572214791 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914989 | GGCACGGACCATTGC[A/G]CCCGGCAATCCTGGA | 114792 |
| rs572219983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97065429 | CGTTCTGATTCCAAA[A/G]ACCATTTCTTGGTTG | 114792 |
| rs572220868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071869 | CCCTGCCTGTAGTCT[A/G]ATGCTAATCAACACT | 114792 |
| rs572226375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046326 | TCATATATTTTGGCC[C/T]AATTAGTCAAACCGA | 114792 |
| rs572230086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97017531 | TAGGTGGAAAAAAGG[A/G]TGGAAGACAGAGAAA | 114792 |
| rs572240086 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079161 | CTTAAATCTACTCTA[A/T]ATTATAAACAAAGTA | 114792 |
| rs572257945 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023016 | AAAACCATCAGATAT[C/T]ATGAGAACTCACTGA | 114792 |
| rs572259468 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96951604 | AGACAATATTAATTG[C/G]TCACTATTAATATTG | 114792 |
| rs572275003 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034916 | AATCTTCAGGGTTTC[C/T]TACGTATATAATCAT | 114792 |
| rs572282978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058948 | AGCATTCTTTTGGTC[C/T]TTAAAACAGTTTTTG | 114792 |
| rs572311962 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077881 | ATACAAAAAGCATAC[A/G]ATGCGAAATCTACTT | 114792 |
| rs572318620 | in-del | -/GTT | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923988 | TGGTATGGTTCTGTG[-/GTT]GTTGTCTGTTTGCGG | 114792 |
| rs572322798 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96903239 | CATAAATATGGAGAC[-/A]TTTTTTTAAATTGAA | 114792 |
| rs572327404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97080534 | TGCAGTTAAAGGGTG[C/T]TTGCAGTGACAAGTG | 114792 |
| rs572330511 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059929 | CCAAAGAAACAAACT[A/G]TAAAGAAGGGAGGAA | 114792 |
| rs572374915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108320 | GTGCTTTCTCAGTGT[A/G]ATGCCATTATTTTAA | 114792 |
| rs572375554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018152 | AATTAATATTGAATC[A/G]AAACTTTTTTCAATG | 114792 |
| rs572376019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959095 | GTGGGGTTTAGCACC[C/T]AGAGAAAGATGAGCG | 114792 |
| rs572380939 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944543 | TATGAGTTTGATGAT[G/T]CTATATATTCATATT | 114792 |
| rs572401018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907708 | ACAACTTAACTCGCC[C/T]AGCTCATTTCTGTAT | 114792 |
| rs572414137 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914095 | CTGGCTTTGAAGAAA[G/T]CGGGGGAATCTACAA | 114792 |
| rs572415962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011510 | CATAATGAATGAGAA[A/G]AGTCTCTTTAAAAGA | 114792 |
| rs572435908 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047745 | ACAAGAGGTCAGCCA[A/C]CCAGGAGCAGGCAGG | 114792 |
| rs572450399 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074571 | CTTATTCGTAATAAT[A/G]ATTAAGACAGTCTGT | 114792 |
| rs572453463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96915921 | TATAAAGGTGCTCCC[C/G]TTTCCTTTCCCAAAA | 114792 |
| rs572484167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003839 | TCTCTATTCTGTTCC[A/G]TTGGTCTATGTCTCT | 114792 |
| rs572492913 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103427 | ACCATGTTAGCCAGG[A/C/G]TGGTCTCGATCTCCT | 114792 |
| rs572494096 | in-del | -/CAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904339 | AGAGCAAGACTTTGT[-/CAA]AAAAAAAAAAAAAAA | 114792 |
| rs572502143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97102385 | CAATGTGATACAGAA[A/G]GGTTTTCTTTTATTG | 114792 |
| rs572505458 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97087735 | CTACTATGTACTGAT[A/G]ATGTCATCTGGGACC | 114792 |
| rs572510950 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078512 | GGAAAAATCTGTAAT[A/C/T]CTATTCAATTTGGAC | 114792 |
| rs572516213 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908470 | TCTGCCACATGCACA[A/C]CCCTCTGCATTTATA | 114792 |
| rs572517995 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96959710 | GGGCCTCCTTGGGAG[A/T]CACTAGCATGCGGTG | 114792 |
| rs572519552 | in-del | -/CATA | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141946 | TCATACTTTTTCCTT[-/CATA]TTTTCTTCACACTTT | 114792 |
| rs572553595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095700 | TGATGGAGCATGTGT[C/T]ATTCATTGATAAAGC | 114792 |
| rs572570495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976515 | TTCAGGATCAAAGAC[C/G]AAGCTATAAGACAAT | 114792 |
| rs572574754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990992 | ATCACAGACCCGTTA[C/G]TAATGGGAATGTTTA | 114792 |
| rs572585818 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139863 | CCCAGATTTTTCACC[A/T]TGGTTACTCTGACCT | 114792 |
| rs572600857 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97044716 | TCTGTTCAGATTTTT[A/T]ATTACTTTTTTATTC | 114792 |
| rs572603909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986573 | AGCCTTGGCAATGGC[A/G]GGCGCCCCTCCCCCA | 114792 |
| rs572607270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997683 | GGTGGAGGCTGTAGT[A/G]AGCCATGATTACACC | 114792 |
| rs572607786 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977108 | ATATAGTGATAGCTG[A/T]TTAAATGCCACTTAT | 114792 |
| rs572629512 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029393 | TAATTTTTAGCATAT[A/G]AGATGGATCTTTATG | 114792 |
| rs572660194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96991605 | CCTGCCCATTGAGGG[A/G]TAGCAGGGTGGGGAC | 114792 |
| rs572707826 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899864 | GATGCTGCTTAGAAT[G/T]AAGCTTCCATCTGAG | 114792 |
| rs572728800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116859 | TTTCTCCTACTGTGA[A/G]AGGAAATACATTTTC | 114792 |
| rs572763279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97067247 | GAAAGGGATACCTGG[C/T]ACTGTGTGGGCTCCT | 114792 |
| rs572770610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900498 | CTCAGCACACGTGGT[A/G]GTATTGTTAGATTTA | 114792 |
| rs572786937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124519 | GTAATAGCTACATTC[C/T]AATCCATTGGTTGTA | 114792 |
| rs572837093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97117606 | TAAAGATGTTAGAGT[C/T]GAATTGTACAGGCTC | 114792 |
| rs572845361 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932429 | AAACTCATGCACAGC[C/T]CTTAGGCCTTTCTAT | 114792 |
| rs572857879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968349 | AATGCATAGGGCAGC[C/T]CCCTACAGCAAAAAA | 114792 |
| rs572892216 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040504 | TCACCTGGAGGGCCT[A/G]TTACAGCACAGATTG | 114792 |
| rs572898511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110426 | ACTTCCACGTTCACT[G/T]CATTCAGAAAACTAA | 114792 |
| rs572921948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018952 | TTTTTAAATGTAGAC[A/G]GAAGATATGGATAGT | 114792 |
| rs572926429 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993368 | GTTGGGGTGGTAAGG[A/G]AAGCTGGGCCATGTA | 114792 |
| rs572937961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96925158 | ATGCAGCCTCTGCCC[C/G]TGTCGTCTAACGGGA | 114792 |
| rs572949146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126284 | GGTCCCATATCCTTG[A/G]TATTTTATTATCTAA | 114792 |
| rs572958114 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019330 | CCAATAACTGCAGAA[G/T]GGAGGTAAAGAAGGC | 114792 |
| rs572964030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97013283 | CTGAGCTAGTGTTAA[A/G]TAACTTTTTATTAGA | 114792 |
| rs573024147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961509 | TTACTGGCTGGGCTC[C/G]TTCTGCCTGTATGCA | 114792 |
| rs573027080 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997268 | GTACCCTAGAACCCA[C/T]AGTGCCTGGCCCACA | 114792 |
| rs573044640 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910456 | AGCACTCTAATTTGT[G/T]TTTATTATTTTTACA | 114792 |
| rs573053030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006978 | TGTCTTGGGGATGGT[C/T]ATCTCATATAGTGTC | 114792 |
| rs573054358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020174 | TCTCAAACTCCTGAC[C/T]TCATGATCCACCCGC | 114792 |
| rs573059604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940798 | CGTTATTGGATGCTG[C/T]ATATAGAAATGAGGT | 114792 |
| rs573069486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911269 | ATAGAAAATCTTGAC[G/T]TCTCTTGCGAAGAAA | 114792 |
| rs573069970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055242 | TAAGGAAAAGTCACC[A/G]TCCATTGAGAAAATA | 114792 |
| rs573071425 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120674 | AAAAGTGTGTGTTGC[A/G]GGAGTAAGTAGTAAG | 114792 |
| rs573075745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040955 | TTTCCTGAGGCCTCC[C/G]CAGTCATTCTGAACT | 114792 |
| rs573084778 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113639 | TTCCTCACATGGGCT[C/T]CAAAATATTCCAGTT | 114792 |
| rs573090310 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999735 | TTGATATTTTTATTA[C/T]AGTAGCTATTGGTAC | 114792 |
| rs573103052 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001093 | ATTCTATATGATACT[A/G]TAATGGTAGATACAA | 114792 |
| rs573109742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901726 | CTTCCTGATTCTCTC[C/T]CTCCTCCCACCCTCC | 114792 |
| rs573148472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090183 | AATGTAGAGTTTCCA[C/T]ATTAAAATGTATTGA | 114792 |
| rs573149786 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082516 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCAT | 114792 |
| rs573174682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041701 | ATTGTTCTTGTTACT[C/T]ATTTTGATGTTAAAA | 114792 |
| rs573181194 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961120 | CATAGCAAAGAAGAC[A/G]TATTTGGGGTTAAAA | 114792 |
| rs573211528 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082469 | ATACAGAAAATTAGC[C/T]GGGCATGGTGGCGGG | 114792 |
| rs573212551 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084862 | AGCCCTTGAAACCAG[A/G]GACCCCTTTCACTCC | 114792 |
| rs573219725 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034471 | GCATGTTCTTTTTGT[A/T]TAAGATTTCTTTGGC | 114792 |
| rs573226258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954278 | GATATGGAAGACTAC[A/C]GTGGAAAAAATTGTT | 114792 |
| rs573226638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96945645 | TATGGGATCCTGAGT[G/T]CACAACATTGGTGAC | 114792 |
| rs573262974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939721 | AAGGACTGCACACAG[A/G]CCTATAAAGATAGGT | 114792 |
| rs573267779 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015619 | AGGAGAGCATAAAAG[A/T]TTGGAAAATTTGCAG | 114792 |
| rs573299248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049696 | TGACATGGAAAGTTT[C/G]AGAAGTGTGAAACAA | 114792 |
| rs573304682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988223 | ATAAAGGGCTAATAT[C/T]CAGAATCTACAATGA | 114792 |
| rs573312309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946780 | TATATTCCCATCTTT[C/T]CCTTTACTATTCCTC | 114792 |
| rs573319073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939996 | TGGATTGAATATTGA[A/G]GGTGAGGGAAGAGAA | 114792 |
| rs573326295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984004 | TCTCTCCTGCTTTCT[C/T]TTGTGGGCATTTAGT | 114792 |
| rs573333451 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984428 | GAGTTCAATTCCTGG[A/G]TATCCTTGTTAACTG | 114792 |
| rs573337845 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96920180 | AACATGGTCAGGGAA[A/C]GGGACCTGGTCAAGG | 114792 |
| rs573357434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96934243 | GATTACTGGATCTTC[C/T]ATACTTACTGTGTGA | 114792 |
| rs573360210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97050382 | TTTCTGGAGAGAGCA[A/G]GGTGACTCCTAAGCA | 114792 |
| rs573363387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96946985 | TAAACTTCCTTAGTA[G/T]TCATTGTGAAAAAAG | 114792 |
| rs573378983 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932309 | TGATTTAATTTTGCC[A/G]TAGCTTATCTTCTTT | 114792 |
| rs573423253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043293 | CAACTTTTTTAGATT[C/T]AGCATATAAGTGAGA | 114792 |
| rs573460372 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938091 | TTAAAACAAACAAAC[-/A]GAAAAACCCTTAAAG | 114792 |
| rs573461143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014898 | ACCCAAATCTCATCT[C/T]GAATTTTAATCCCCA | 114792 |
| rs573466572 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896987 | ACTGGAGTGCAGTCG[C/T]GCGATCTCGGCTCCC | 114792 |
| rs573477289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105380 | CTGCTGTTTGATGGA[C/G]GTTCAGGAGTGAGTT | 114792 |
| rs573484455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069375 | CTCACTAGGGAGTTA[A/G]GGAGAATTCTGGGTG | 114792 |
| rs573485826 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043735 | TGTTATCGATTGTCT[C/T]TTTTTTATAGTAGGG | 114792 |
| rs573495698 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97062937 | CGTTATCTGAAGTAT[A/C]TGAGGGAGTGGCCCA | 114792 |
| rs573517996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056295 | TATTTTTAGTAGAGT[C/T]GGGGTTTCACCATGT | 114792 |
| rs573539096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948888 | TTTTCTGACTCATGC[A/G]AAAAAGTCATGTAGC | 114792 |
| rs573539317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940976 | TAGATGATGTGAAAT[A/G]TACAAATCAAAAATA | 114792 |
| rs573555952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056511 | CCAGGTGGCTTTGCT[C/T]GCTCCTCCCCACTCT | 114792 |
| rs573567926 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96925440 | CATTCAACTTCAAGA[A/C]AAGCCGTAATTGCAC | 114792 |
| rs573570266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963499 | TACCCTGTGTTTAGA[C/G]CTACTCCTGCATCTG | 114792 |
| rs573581928 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96964596 | AGGCGGAGCTTGCAG[A/T]GAGCCGAGATCGCCC | 114792 |
| rs573612735 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96955509 | AGAGAAAGATGAAAA[A/T]AATATTTTAAATTAA | 114792 |
| rs573652624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912862 | TATTTGTCTGTCTGC[C/T]CCTCTCCCTACCACC | 114792 |
| rs573652682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001514 | TCTTTATCACTCAGA[A/C]TGAAGTGCAGTGGCA | 114792 |
| rs573668415 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971685 | CAGGGACAGCAGTTC[A/G]CACAGGCAGCCTGAC | 114792 |
| rs573669237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904521 | ACACATGGCTAGACA[C/T]ACCAGGTTCCTTGAT | 114792 |
| rs573684408 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056849 | CTCGACACCAGGCTG[A/G]GCAACATAGCAAGAC | 114792 |
| rs573699081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099003 | TTTATCTTATAGGTT[C/T]GCTATGTTTTTAAAG | 114792 |
| rs573706331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97071601 | GCTGCCCAAATTCGC[C/T]TTTGCCCAGTCTCAC | 114792 |
| rs573740413 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136403 | ACAACCCAAACAAGA[C/G]AAAAGCAGAGATACT | 114792 |
| rs573763325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96972891 | CTTGGTGAAGTGGGC[A/G]TGCTCCCTTCCAGCT | 114792 |
| rs573770290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035988 | TTTACTTGATATTGT[C/T]CCATAAAATCCATAG | 114792 |
| rs573770974 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064713 | TCAATTTATGCTCCC[A/G]CTATCTCATCCAGGT | 114792 |
| rs573773864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97091564 | TTTCCCACCTGCCCA[A/G]TGCCTTCCCAGTGGG | 114792 |
| rs573783009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036374 | CCCATTTCTTTGGGA[C/T]CATTACTGGAAATTA | 114792 |
| rs573791985 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97019306 | GATTAGTGTGAAGAG[-/C]CCTTGGACCCAATAA | 114792 |
| rs573795967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96973853 | TCAGCCTCCTGAGTC[A/G]CTGGGATTAAGGTGC | 114792 |
| rs573804827 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095306 | TTTGGAGTGAAGCCC[C/T]ATATAAATCCAATAA | 114792 |
| rs573808961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97029499 | TTTACTGTTTTAGTT[C/T]GTCTTGTGATATTTT | 114792 |
| rs573837222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97092284 | GTGAGCCACCGTGCC[C/T]GGCCAATTCTCTTTC | 114792 |
| rs573847901 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996996 | ATGGGTTGGGAGGTA[C/G]GTAAACAGGACATTG | 114792 |
| rs573849219 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014266 | CGCCACTGCACTCCA[A/G]CCTGGGTGACAGAGC | 114792 |
| rs573853032 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100502 | AGTTTATGGGTTCCC[C/G]CATGCCAGTCTCTGT | 114792 |
| rs573867672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127975 | TCTACATTTCATGTA[C/T]ACCCAATTACTATTT | 114792 |
| rs573868397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030119 | TGATAAAATGGGAGT[C/T]GCAGTGGTTTTGCCT | 114792 |
| rs573885421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966336 | TTAAAAACAAAGACA[C/T]GGGATGGGGGCAGGG | 114792 |
| rs573890033 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073197 | GCAAATTTTCTGCCT[A/G]CTTCAAATTGACAAC | 114792 |
| rs573890385 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985545 | TTTTCATATAGTCCC[A/T]TATTTCTTGGAGGCT | 114792 |
| rs573914901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101301 | ATCTGTCTACAAAAG[A/G]CTTAAACTTCCAGAT | 114792 |
| rs573920708 | in-del | -/ACAAA | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129886 | GACTCTGTCTCAAAT[-/ACAAA]ACAAAACAAAACAAA | 114792 |
| rs573926669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980258 | TTCTCAAAGGGAATG[C/T]TCCAGCTTTTACCTA | 114792 |
| rs573943460 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110388 | TTAAGAGATGCAATT[C/T]ATGACGTAGCAGAAG | 114792 |
| rs573944806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989210 | CAGTGGCCTATATAC[A/G]TAAGTGTTTTTGTGG | 114792 |
| rs573977527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094036 | AATATATTGAAATTT[C/T]AGAAATGTATGCAGC | 114792 |
| rs573981446 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96996101 | GTTACAGGGCCCAGC[A/G]TGGGCAGCCCTGGGC | 114792 |
| rs573982831 | snp | C/T | 1.7031e-05 | 0.00291808 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113767 | TCTCCTCTCATCTCA[C/T]TTCCCTCTGTTTCAG | 114792 |
| rs573995752 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953617 | CCTGGGTGACAGAGT[A/G]AGACTCCATCTCAAA | 114792 |
| rs574034290 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034324 | CAAAGATCAGTTTAC[C/T]ATAGATGCATGGATT | 114792 |
| rs574039954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96929454 | TCTGCCTATAAGACT[G/T]CTTATTATTTCAGAA | 114792 |
| rs574041603 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011587 | ACCTTTAGAAACTCT[A/G]TAAACTCATCTAAAA | 114792 |
| rs574051212 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022743 | CCAAAGTGCTGGGAT[C/T]ATAGGCATGAGCCAT | 114792 |
| rs574052158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97057559 | TTTACACCCCCCTCC[C/T]GCCCCCATTTCAAAA | 114792 |
| rs574056790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121447 | GTCCATTCTTCTCAG[A/G]GGTGAGAAGAGACAC | 114792 |
| rs574069905 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009690 | TTTGATGGAAGTGAA[A/G]TGTGATCTTGCTGGA | 114792 |
| rs574114540 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024452 | TCCTTTTGAAACTGA[A/G]CACATTTCATTAAAA | 114792 |
| rs574125650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016308 | GGGGACTGTACCCTG[C/T]GAAGCCACAGGGGTG | 114792 |
| rs574125944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023574 | ATTCATTTAAAATCC[A/C]GGGCAACAAGGATTG | 114792 |
| rs574139603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97122551 | GTGTAGCCCTCTAAA[C/T]AGTGACTAATAGGAA | 114792 |
| rs574142286 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96921395 | CACTGGCGCTGGCTC[A/C]TGATGAATAGGATGA | 114792 |
| rs574154971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97003121 | TCCTACCAGCAGTGT[A/G]TAAGTATTCCCTTTT | 114792 |
| rs574160740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97016724 | GGCCAGGGGCAGAAT[C/T]ATATGGTTTGGGCTG | 114792 |
| rs574181653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958548 | TCAAGTGGTAAAACA[C/T]AAGGCTGGTAGTGTT | 114792 |
| rs574181759 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980090 | GAGAGTTCTAAGTAT[A/G]GAATCACATCATCTG | 114792 |
| rs574205238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96922015 | AAAGAGGTTTCTTTC[A/G]TGTAAGACCTCAGTC | 114792 |
| rs574207460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97123336 | CAGTATGCACTCATC[C/T]ATTTGTCACAACATT | 114792 |
| rs574207467 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97114939 | AATCCATTTTTCTGG[G/T]TATATCAATAGGTAT | 114792 |
| rs574233312 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137702 | ACCACGCCTGGCTAA[G/T]TTTTTGTATTTTTAG | 114792 |
| rs574255595 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97086136 | TTGTAGGGTGCCATG[A/C]CTCCAAGATTTCACA | 114792 |
| rs574272980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138297 | TAATCCCAGCACTTC[A/G]GGAGGCTGAGGTGGA | 114792 |
| rs574282597 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138546 | AAACAAAAACAAAAA[C/T]AAAAACAACAAAAAA | 114792 |
| rs574286274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907573 | CAGGAAGCTCTTGAA[A/G]CTATGTTTCACTCTA | 114792 |
| rs574319093 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923008 | AGTGAGCCGATACTA[C/T]GTGGCAGACATTGTG | 114792 |
| rs574319425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914359 | TGGTTAAGTCCTTGC[G/T]TAACTTTGACTTTTT | 114792 |
| rs574329411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96950696 | CTGGCCAGATGTATT[C/T]TCATGGAAAACCAAA | 114792 |
| rs574334477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018239 | AACAGAAGATGACAG[A/G]TATTAGACCAAATAT | 114792 |
| rs574347391 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898332 | GAACCAGGGTCAAAC[C/T]GGGCTCTCAAGTTGC | 114792 |
| rs574355185 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079863 | AAATGAAACCTTTTT[A/C]GAAAAAAAAAAGAGT | 114792 |
| rs574365948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011557 | AATTATAAAATTGTT[A/G]AATTTCTTGTCACAA | 114792 |
| rs574374820 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129465 | TTAAAGTCATATTTG[A/G]TCTTCATTTAATTTT | 114792 |
| rs574388104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97037290 | AAAACATAAAACTCT[C/G]TAATGCAGTGAGATG | 114792 |
| rs574407891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045205 | TGGATCACAAATTCA[A/G]GATTAGCCCAGCCAA | 114792 |
| rs574414797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916077 | CAGCAGATTCAGAGA[A/G]ACTCCAGAGGTGCCT | 114792 |
| rs574438692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96942697 | TGTGTGTGTGATTCA[A/G]AATATCCCTTCAGGG | 114792 |
| rs574460064 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012340 | AGAGTCACAGTCAGA[A/G]GAGTCAGGACAGAAG | 114792 |
| rs574461615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97024871 | CTTTATATGTATTTG[C/T]TTCAAATATATATTG | 114792 |
| rs574469143 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003086 | AAAGTTCTGTCCACA[A/G]TGGCTAAACTAATTT | 114792 |
| rs574489777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032332 | TTAATTGTATTGATA[C/T]AAAATGATTACCAAT | 114792 |
| rs574496373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96981759 | TGTTGTATCTTTGTT[C/T]TCATTATTTTTAAAT | 114792 |
| rs574513343 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950848 | ATGACTCTTGTTCTA[C/T]TTTGATTCCACAACA | 114792 |
| rs574529545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96908581 | AAGACGAAAAGAGAA[A/G]AAGACCAAAGCTTCT | 114792 |
| rs574530368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97025566 | ACTGTGGTTTGAAGA[A/T]GTGGAGGAGAGGAGG | 114792 |
| rs574530908 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96930541 | AATCTCAGTACTTAT[G/T]AATTCCTTCCCTCTG | 114792 |
| rs574532576 | in-del | -/TGTT | 0.00557542 | 0.0525036 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982677 | CATGATTTGGTTCTC[-/TGTT]TGTCTGTTACTGGTG | 114792 |
| rs574540632 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122526 | TACTTTTTTTAAGGG[A/C]TAACAATGAGTGTAG | 114792 |
| rs574548322 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947687 | AAACTAACACTTTCA[C/T]GGATTTTATGCTCTT | 114792 |
| rs574549280 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118913 | AGTAGTGCAAAGCAG[C/G]GAGTGACTATTGCAG | 114792 |
| rs574551031 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982412 | CTTGGTAGATTTTTC[C/T]TTATCCCTTTACATT | 114792 |
| rs574552343 | snp | A/G/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97072818 | CTTCTTTAATTATGG[A/G/T]CAATCTTCTGGGAGG | 114792 |
| rs574578124 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109166 | TTGACCAGAAACCCC[C/G]GTGTAATTTGTGTAC | 114792 |
| rs574622530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96931310 | TCTGATGACCCAGGA[A/G]TGCACATGAGATTAG | 114792 |
| rs574630432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97073615 | GAAACACATATTGTC[C/T]GATTGGATTCCTTCT | 114792 |
| rs574636641 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924241 | GACTCCCTGGAACAC[C/T]GAGTTAGGGCCACGG | 114792 |
| rs574637696 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931619 | CAATTTCATAATTCA[A/G]ATGCATTTTTACTAG | 114792 |
| rs574648111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96944595 | ACTTGCCAACTCATC[A/G]TGTCATTTAGTCTTA | 114792 |
| rs574650601 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96937584 | GCTGACTCCTCACAC[A/G]TTTTCTATTAATGAA | 114792 |
| rs574654698 | snp | A/G | 1.66974e-05 | 0.00288936 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976120 | CACCCTGATTGCTGA[A/G]GAACAGAAATTCCAT | 114792 |
| rs574661101 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914745 | GGAGTGCATTGGCTA[G/T]TTATAGATGCAATCC | 114792 |
| rs574679584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97053227 | AAATGAGGCAGAGAA[A/G]ATAATAAGTAACTAG | 114792 |
| rs574693649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066108 | AGGTTATAAGACTTC[A/G]AAAGTGTGTGTTTGA | 114792 |
| rs574705813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97004880 | GTCTGGTTTATTAGT[A/G]TTTTGTTGTGGATTT | 114792 |
| rs574715532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980538 | GGTGGATTAGCTTTT[C/T]GATGTGCTTCTGGAT | 114792 |
| rs574768177 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959745 | CAGGTTCTGATCCTT[A/G]GCCTTTGGTTTCTAT | 114792 |
| rs574768221 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936591 | TCACAACTTCCCACT[A/G]CCATTCTTGTCCCAG | 114792 |
| rs574773793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97054280 | TCTAAGTTAACTTGT[A/G]AATATTTTATTTTTG | 114792 |
| rs574786746 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967707 | TAAAATGTATATTCT[A/T]TGGCGAAAACAGACA | 114792 |
| rs574795965 | snp | G/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139979 | CATTATGAGGATTAG[G/T]CGAACACTTTGTAAT | 114792 |
| rs574817316 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074772 | TTTAAACATTTTTAA[A/T]CTGATTTTGCCTATC | 114792 |
| rs574820665 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964947 | AGGTTTGGGATACGG[A/T]TGATCCCATCACCCA | 114792 |
| rs574831030 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96899966 | CTAGAATGTAAATTC[G/T]GAGGACAGAACTTTG | 114792 |
| rs574871563 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:97118416 | CTGAGATTAGGAGTT[C/T]GAGACCAGCCTGGCC | 114792 |
| rs574875448 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968176 | CTCTGCACTCCCTAT[A/G]TGAGTCTGTTGCTCT | 114792 |
| rs574883222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900762 | GCCCAGGACAGCCCT[C/T]AGAGGTTTCATCAAT | 114792 |
| rs574939585 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97074676 | ATTTAAAGTCTGCAG[A/T]ACTGGGCTAATTTTC | 114792 |
| rs574946635 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97061646 | GATGGGTATGTTTCT[G/T]AAATACCTAAATATA | 114792 |
| rs574965642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97088648 | TATGTTAATTAATTT[G/T]ATTGTGGTAATCATT | 114792 |
| rs574992616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982997 | TTTTTGCCCATTCAG[C/T]ATGATATTGGCCGTG | 114792 |
| rs575002291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932573 | TCAATTTCCCCCCCC[C/G]CCTTTTTTTTTTTGA | 114792 |
| rs575009542 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062655 | TTCATTAGCATTTTA[A/G]TTAAGTAACTTCATG | 114792 |
| rs575070526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124567 | GCAGAGTCTGATACA[C/T]ACAGTAGTGTAAGTA | 114792 |
| rs575094025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96962143 | TGCTCACTATTATGG[C/T]TTAATAAGATATTTA | 114792 |
| rs575100806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986910 | ACACTCCCCAGTGAG[A/T]TGAACCCAGTACCTC | 114792 |
| rs575105463 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97110571 | CGGGTTGAAAACCCA[G/T]TTTGTGTTTGCCAAG | 114792 |
| rs575126386 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983530 | TTTATTTGGTTGGTA[A/G]GCTATTAATTGTTGC | 114792 |
| rs575137582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987160 | CTTTTCAAAAAACCA[C/G]CTCCTGGATTCATTG | 114792 |
| rs575165013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977186 | ATCTCATTTGATCCT[C/T]ACAACAACCCATTGT | 114792 |
| rs575166671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103723 | GTGCACTTTCATACA[G/T]GCAAACATTCACGCA | 114792 |
| rs575174033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090809 | AACTCATGTCTTCTA[A/G]TTCTTGAGCTATGTC | 114792 |
| rs575187712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994045 | TGGAGGGAGATACTA[C/G]TCTGTCTTCCAAGGC | 114792 |
| rs575191293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082994 | TTGTTCTTGCTCTCC[C/T]CCGCAACCTACTGTG | 114792 |
| rs575201681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97055392 | ACTAATCTCCCCCAC[A/G]TAGGGTCCAGATCCA | 114792 |
| rs575216511 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133510 | TGGGAAGATTTTTAA[A/C]AACTGCATCAATATC | 114792 |
| rs575278147 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106555 | TGAGACCAGCCTGAC[C/G]AACATGGTGAAACCC | 114792 |
| rs575312695 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021376 | GATGATGTAGTTTCT[G/T]TTGGAAAGCTGGCAG | 114792 |
| rs575344671 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119701 | TAAACTTCATTCCCC[A/G]AATCTGAGCTTATCA | 114792 |
| rs575348153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111137 | AGATGCCTTCAGTTG[C/T]CCCAGGACTTTATTC | 114792 |
| rs575364995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007102 | CTAAGTTGCTTGTTT[G/T]TTTCTCTCTCTCTTT | 114792 |
| rs575367503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917709 | TTCTCTGTGTGCCAG[G/T]GATCAATTCCTGTGA | 114792 |
| rs575382253 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984940 | CTGGTTATTTTGCTC[A/G]TTAGTTGATGCAGTT | 114792 |
| rs575386023 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014089 | TGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCAA | 114792 |
| rs575386378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014965 | GTGATTGAATCATGG[C/T]GGTGGTTTCCCCCAT | 114792 |
| rs575406729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112217 | TTTAATATTCTATTT[A/C]TTTGCTTCATTCTTT | 114792 |
| rs575409696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97049566 | TGAAACCGTAGAAAG[C/T]GAAACCGTCGATAAC | 114792 |
| rs575425948 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082485 | GGGCATGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 114792 |
| rs575427211 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045721 | GTTGATGTGTATGTG[C/T]GTGTGTGTGTGCACG | 114792 |
| rs575431256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96918536 | CAGGTACATTAATCT[A/G]CATTATACTACTGTA | 114792 |
| rs575466640 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092083 | CAACCTCCGCCTCCC[A/G]AGTTCAAGTGATTCT | 114792 |
| rs575472315 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97015771 | CCAGGGCATGTCAGA[G/T]ATCTTGGTGGCAGCC | 114792 |
| rs575494595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96902423 | TGTCTGGGCATGTTC[C/T]TTGCATACTTTTTAA | 114792 |
| rs575497691 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934271 | TGAGAATCTGCATTA[G/T]TATTGAGTCATTTGT | 114792 |
| rs575505128 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998009 | CACGTGGTGTTTATT[-/A]CATAAAGGATAAATG | 114792 |
| rs575511272 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008403 | GTAGTGCTCAGATCA[A/G]ACTAGCCCCATCTCA | 114792 |
| rs575532624 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980070 | TATGGGGCAGAGACT[A/C/G]TGTGGAGAGTTCTAA | 114792 |
| rs575533772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060335 | GAGAGGGAAAATAAA[A/G]AGAAAAAGAAGACAG | 114792 |
| rs575535455 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039018 | TTGCTTGGACCCAGG[A/C]GGCGGAGGTTGCAGT | 114792 |
| rs575540989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96911391 | ACTCAAGCATTTTCA[A/G]CTTCCCCCCATGGTT | 114792 |
| rs575547394 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018544 | AGGCAGAGGTTGCAG[C/T]GAGCCGAGATCACAC | 114792 |
| rs575550947 | in-del | -/A | 0.338814 | 0.233692 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105766 | TTGTAGACCAAGACA[-/A]AAAAAAAAATACTTG | 114792 |
| rs575554068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913009 | CTGAATGAATATAGA[C/T]GCAAAATTATTTCAA | 114792 |
| rs575579011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127104 | TGTACTATGTTCACT[C/T]TCACTCCCTAATACT | 114792 |
| rs575594613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127736 | ATTGTCCTGTTGTAA[C/T]GTCCTTCTGGAAGGG | 114792 |
| rs575597854 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982095 | GTTGAGTTCAGGTCC[G/T]GAATATCTTGGTTAG | 114792 |
| rs575599279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008907 | TGTGCTTAGCCGGCC[A/G]TCTTGGCTCCCCAGC | 114792 |
| rs575609385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043316 | AAGTGAGATCATGAA[A/G]TATTTGTCTTTCTGT | 114792 |
| rs575617396 | in-del | -/T | 0.440333 | 0.16209 | intron-variant | KLHL32 | GRCh38.p7 | 6:96954313 | TTTTCTTTCCTTCAA[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs575621792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028778 | CATTCAATAATGGTT[C/T]AGCAAATGTATTCAA | 114792 |
| rs575634684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97034596 | ATGTATAGATCATTT[C/T]GGGTAGTATGAACAT | 114792 |
| rs575654219 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986677 | CCTCCAAGCAATGCA[C/T]GGGATATAATCTCCT | 114792 |
| rs575654590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96984453 | TAACTGTCTCATTGA[C/T]CTGTCTAATGTTGAT | 114792 |
| rs575664364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913516 | TCCTACCTTGACTGA[C/T]GTCAATGTGACATTG | 114792 |
| rs575664636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904632 | TAATAGCGTTTTTAA[C/T]GAAGCTCGATCACTG | 114792 |
| rs575678887 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947273 | CATTCAACCTGTGTA[A/G]GCCTGAAGCTCACGC | 114792 |
| rs575700978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021983 | TGGACCTTCAAAACA[C/T]ATCCAGACTCCAGCC | 114792 |
| rs575705034 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960812 | AGCTGGAAGCGGGGG[A/C]TTCTGGGTCATAGGT | 114792 |
| rs575707347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97021359 | TGAGACCCAGGAGAG[C/G]CGATGATGTAGTTTC | 114792 |
| rs575728608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905410 | CTCCGTCTGTCTGGT[C/T]CTTTCTCCCTTTGTA | 114792 |
| rs575729546 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085646 | TTTCCTGATAAAAAT[G/T]GTTTCTTAAACAAAA | 114792 |
| rs575749510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97137278 | ACCTAGTCAAAACAA[C/T]TGTAAATGTGACACT | 114792 |
| rs575750490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96940183 | GAGCTGTCTTTAGGA[C/T]GTTGAGATGAAGATA | 114792 |
| rs575755629 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:97036429 | TTTCCCTGACATTTC[A/C]TGTTCCTTGTAGCCT | 114792 |
| rs575759806 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928442 | AGAGGATGCAACTGC[A/G]GATGGGTGGGAGGGG | 114792 |
| rs575776985 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069508 | ACATCAGGGCTGAAG[G/T]TATCTGAGTGCTGTT | 114792 |
| rs575786631 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062325 | CTATTCCCCATTCTC[C/T]TCCTTAGGCCATGCC | 114792 |
| rs575788672 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KLHL32 | GRCh38.p7 | 6:96941902 | GGAAGTGGTTGTCCC[A/G]TAACTTTTTGAGAAT | 114792 |
| rs575816586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96935538 | CTAACTGTGAAACCG[C/G]GTCTATCATCAATTG | 114792 |
| rs575834120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062489 | GATATAAAGATTTTT[C/T]AGAATAAGATGAGTG | 114792 |
| rs575843902 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941626 | TAGTCAACTTCACGT[-/A]AATCCACGAAAGCCC | 114792 |
| rs575844881 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106702 | TGAGCTGAGATTGCG[A/C]CACTGCACTCCACTC | 114792 |
| rs575859799 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931386 | AGAAGAACCTAGACA[A/G]CAGCAGGAACTGCTA | 114792 |
| rs575892879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971091 | TAAGAAATGAGAATC[C/T]TTATCCCACTTAGTT | 114792 |
| rs575894153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099059 | TCATCTTAAAGAAAG[C/T]ATAACTCATTTTGTC | 114792 |
| rs575901304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007152 | TAGATTTGGTCTCTT[C/T]ACATTATCCCATATT | 114792 |
| rs575912986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96936252 | ACATGTCTACATTTT[G/T]CATGGCCGTTCATTT | 114792 |
| rs575933710 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917626 | CAAGGGTCTCAGCAG[G/T]AACTTCAACTGGGCC | 114792 |
| rs575958855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97001609 | AGTAGTTGAGACCAC[A/G]GGCATGTGCCACCAC | 114792 |
| rs575960700 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129253 | CTTCCCTTACAGTTT[G/T]GTGAAATGGTGAAAT | 114792 |
| rs575985202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96956706 | CAGCTTGCTGAGCCT[C/T]TCCTTTTTCTTCTGG | 114792 |
| rs575989460 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065237 | CTCCCTGATTTGCTG[C/G]TCAGGAAAGGCCCCA | 114792 |
| rs575992984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043868 | GAGAAGTGTCTATTA[C/G]GTCCTTTGCCAGCTT | 114792 |
| rs576019124 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948470 | AATTTTGTGATGTAG[A/G]TGTGTCCTTATGTGG | 114792 |
| rs576020277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058244 | TTTGCTTCTTCATAT[A/G]AGCTTTAGAATCTGT | 114792 |
| rs576043120 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938822 | TCATGTGACCCACAT[A/G]CAGTGATGTATGTAA | 114792 |
| rs576067734 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897188 | CCTCGGCCTCCCAAA[C/G]TGCTGAGATTACAGG | 114792 |
| rs576077990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96948957 | AAACTTTCTTATCTC[C/T]GACTTTAGAATCTTT | 114792 |
| rs576083588 | in-del | -/AAAC | 0.00455579 | 0.0475093 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898702 | GACGTCAGAAAAAAA[-/AAAC]AAACAAACAAAAAAA | 114792 |
| rs576084745 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896363 | CCACTTACTAAAGGA[A/G]TCTCTGAGATTAGAA | 114792 |
| rs576097260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132559 | TATACAAATGTGCCA[C/T]AAAGGAAAATTGTAT | 114792 |
| rs576098185 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96966494 | TTTTATTCTCTCTCT[A/C]TGTTATTTTTTCCAC | 114792 |
| rs576103114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128628 | GCCTTTGTGGAGAGT[C/T]GATAATGCCTGCCAT | 114792 |
| rs576105433 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96965318 | CTTTGTAGTATATAG[C/T]GGATTATGATTCAAC | 114792 |
| rs576125321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078479 | TAAAATAGCCACATC[C/T]GTTGAGTGTTATTAC | 114792 |
| rs576136620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97129287 | ATGTATTCAAAACAT[C/T]GTATGACTTTTTTTC | 114792 |
| rs576141103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96958647 | AGTGGGCCAAGAGCT[A/G]TTGCCTGTATTCATT | 114792 |
| rs576152997 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905690 | ACATTCAAAAACTAT[-/AA]TAGCTATTATTCTTT | 114792 |
| rs576158982 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97079165 | AATCTACTCTAAATT[A/G]TAAACAAAGTACTTC | 114792 |
| rs576165630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97120836 | TAAATCTTTGTTGCT[G/T]TAGATCCTAGCAACC | 114792 |
| rs576165729 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073279 | AAAGATATTCTTCCT[C/G]TTAGCCACTTCTCTT | 114792 |
| rs576183303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085025 | CCATTTCTCCCACCA[C/G]TGTGATGAAAACCTT | 114792 |
| rs576198042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97121551 | CTACTCTAAAATACA[C/T]TGGTGTAGATTAGAA | 114792 |
| rs576230320 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918622 | AACTAAAAATTTGAT[C/G]TATCACCAAGTGTTC | 114792 |
| rs576235053 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96989278 | CCCTTAAGTGCCTAT[G/T]TTAAGCCAGGTCTGT | 114792 |
| rs576242499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97023656 | TGAAATGGAGATTTA[A/G]TTGTAAGTCCCAAAG | 114792 |
| rs576246758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980329 | TGTTAGTTTGAGGCA[G/T]AGTCATATAATGCCT | 114792 |
| rs576253333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928848 | GAGGCTAAGGAGGCT[C/T]TTACAGATACAGATT | 114792 |
| rs576300696 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951395 | AGGAGGAAAGTTTGC[A/G]ACTAATACTCAGAGT | 114792 |
| rs576303789 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980815 | CAGGTTAATAGGTAT[A/G]TTAGTCCGTTCTCAT | 114792 |
| rs576337620 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979478 | TTTCTGGGCTCTCTA[G/T]TCTGTTCCATTTGTC | 114792 |
| rs576360093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986258 | AGAGGAGTATCCGGC[C/T]GTGTGAGGTGTCAGT | 114792 |
| rs576361367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094543 | AATACAGAGTTATGC[A/C]TTCTCCATGGTGAGG | 114792 |
| rs576380762 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003399 | CTGGATAGTAGACCT[G/T]TGTTGGATATATAGT | 114792 |
| rs576382428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020717 | CCTCATTTTCCTCAA[C/T]GCATCAGCATCTCAG | 114792 |
| rs576456314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96974693 | ACAGGAAGTATTTGG[C/T]TAATTTTAAGATGGT | 114792 |
| rs576458177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101400 | AAATCAAGAATAAGC[C/T]TCGAGTTTTATGATA | 114792 |
| rs576469098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97115659 | TATAAACATGTGTTT[C/T]CAATCTTAGTTTTGA | 114792 |
| rs576469803 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107489 | ACTTGTCTGGTTTTG[A/T]TTTCCATTTGTAAAA | 114792 |
| rs576477942 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114685 | GCAATGTAATTGGAA[A/C]TAATATGCCTTTCTG | 114792 |
| rs576486139 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97063307 | AGCAGGACTGGCTGA[C/T]GGATTCGATATAAGG | 114792 |
| rs576487458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982469 | GATGGGTCTCTTGAA[C/G]ACAGCACATCATTGG | 114792 |
| rs576494760 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913893 | GGATAGATTATATTA[C/T]CTGACAAAGGAGAAT | 114792 |
| rs576517717 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998827 | AGGCACCAGAGTATC[A/T]TTCTTACAGTATTTG | 114792 |
| rs576523290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97094308 | GACCCAGAGGCTCTA[A/G]AATTATTTACATTCT | 114792 |
| rs576531021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109304 | AAATATTAATAAATG[A/G]TAAAAGTTGAAAGTT | 114792 |
| rs576532490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97116722 | AGCTCCTCTTAGACT[C/T]GCTAGATCCGTCGTC | 114792 |
| rs576537443 | snp | C/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:97045423 | ATTTGCCCATCTCTA[C/G]AGTAAGATTGAAAAC | 114792 |
| rs576541929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97108175 | GTTTCTTTTCCACTC[C/T]TGCTGGCTTGGCCAC | 114792 |
| rs576550245 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081647 | ACTCCAAGTCAACTC[C/T]AAGTTAGTCCTTTAT | 114792 |
| rs576551503 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051826 | TGATGGATTTTTAAA[A/G]CACATGAACTTTTTC | 114792 |
| rs576575769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96982810 | TTTTCTAGATATACA[A/G]TCATGTCATCTGCAA | 114792 |
| rs576584206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97010984 | TCTGATCTTTAACAC[A/G]TACACCTGCTATACC | 114792 |
| rs576592669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97109794 | TCTAGTGCTGTTTCC[A/G]GTAGTATCTATGTGG | 114792 |
| rs576606938 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098582 | AGTAAAGAGAGTCAT[C/T]AGGTGATCATTCAGT | 114792 |
| rs576609658 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033939 | GGATATTAACCCTTT[A/G]TCAGATATATGGCTT | 114792 |
| rs576614037 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045518 | CCAAGTAAATAATAT[C/G]TGCACTCAGCTGCAT | 114792 |
| rs576616011 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068170 | TTTGCCGTTACCTTT[C/T]CAAAAAAGAAAAAAA | 114792 |
| rs576617080 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97046248 | AGCTCTAAGGAATGC[G/T]GTGACCCCACTTGAA | 114792 |
| rs576638274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97012542 | TTCCAGAACTATAAA[A/G]TAGATTTGTGTTGTT | 114792 |
| rs576657327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990534 | TTTCTGGCTGCAGAT[C/T]TTGGATTGGCACTCC | 114792 |
| rs576701005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97138399 | TACAGATTAGCTAGG[C/T]GTGGTGGTGTGCACC | 114792 |
| rs576703422 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:96990947 | TGGCAGAGGGGCTTT[C/T]GGTTTTGTCTAGGAG | 114792 |
| rs576715942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103458 | GACCTTGTGATCTGC[C/T]CGCCTTGGCCTCCCA | 114792 |
| rs576742886 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96909573 | CCATAATGGACAAGC[G/T]GAGCAGAAACAGACT | 114792 |
| rs576743886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96907674 | CATCAGAAGAGTGAC[C/T]CTGTGATCTTAGGAT | 114792 |
| rs576745554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97038242 | GTAGAGCAAACCCAC[A/G]GAATGGGGACAAATA | 114792 |
| rs576755341 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140040 | ACTGAAATTATAAGG[C/T]ATTTTATTGTCTTTA | 114792 |
| rs576761551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97006318 | CTTTTTTGCCTGATA[C/G]TAGAATAGAAAGCTC | 114792 |
| rs576766757 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029358 | ATTTGAAGATTTTAG[A/G]AAAAAAACAATATGT | 114792 |
| rs576796049 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101443 | AATGGCAAATGAGAA[C/T]GTTGATATACACTGA | 114792 |
| rs576810771 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:97039000 | GAGGCTGAGGAAGGA[A/G]AATTGCTTGGACCCA | 114792 |
| rs576813847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97124284 | GGGAATCTATTAATA[C/T]CAAATAACTGGGACT | 114792 |
| rs576818429 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899694 | ACAATTGGCTGTCAC[C/T]CTTTGGGAATCATGG | 114792 |
| rs576818637 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992243 | TCCCGGGACCCAGGG[A/T]TGCAAAGGTCCATGG | 114792 |
| rs576819371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97128814 | GGCACTGCAGTGAAG[A/G]AAGCTAAAGATATAA | 114792 |
| rs576827171 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931985 | GTTCATAATTAATAT[A/G]GATATCTGAGTGGAG | 114792 |
| rs576829289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97066215 | GATTCACTTTCCCCA[C/T]GGCAGATAGTAATCA | 114792 |
| rs576831039 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967939 | ATTCATTTGAATAGT[C/T]TCACTGGAGGTAAAT | 114792 |
| rs576845666 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941374 | CAAACATGCATTTTG[A/G]TATTTAATTTAAGAG | 114792 |
| rs576853546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96900981 | GCAGTGTTTTGGGTC[C/T]GTAAAACCTAGAATA | 114792 |
| rs576855425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96910339 | GCTATGTCAGAGAGG[A/G]CACACAAAGGGGAAG | 114792 |
| rs576868784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97032421 | ATTGTGTTTTCCTCC[C/G]AACTCTACTAACTCT | 114792 |
| rs576910945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960102 | TACAGAATAGGGGTA[A/G]TAAATAAGCTAGGGA | 114792 |
| rs576912136 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975902 | GAGTGCACTGGAACC[A/C]GTGTTGCCTCAGTCG | 114792 |
| rs576917374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96901655 | ACTTTAGATGACGGT[G/T]TGCTGCACAGATCAT | 114792 |
| rs576930270 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115084 | GCAGTGGTGCCATCT[C/T]GACTCACTGCAACCT | 114792 |
| rs576941425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97018927 | CTGAAACTGACAGAT[C/T]ATATAGATTTTTTTA | 114792 |
| rs576941968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97133881 | ATTTTTCTTAGCATA[C/T]ATGGAACATTTACAA | 114792 |
| rs576949727 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908172 | GTGTATCTGAGACTC[A/C]GAAAATATACTCCTT | 114792 |
| rs576989369 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97103265 | GTCACCCAGGCTGGA[C/G]TGCAGTGGTGCGATC | 114792 |
| rs576995133 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | KLHL32 | GRCh38.p7 | 6:96938286 | GGAAAAAAAAACAAA[A/T]GTGTGGTTCAGGCTC | 114792 |
| rs577005684 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97101705 | ATTAGAATTACTGAG[-/TTTA]TTTGTGTGAAATATG | 114792 |
| rs577020815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96916641 | GAAGGCCTCTGTGCA[C/T]ATAAAAATTAGAATA | 114792 |
| rs577025380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933178 | ACGCCTTTGAAAACA[A/G]CGACATATTTTACTC | 114792 |
| rs577026117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96914396 | TGGGCTCCAAATTAT[C/T]GGCTCTTCAGCCTTA | 114792 |
| rs577037105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96968271 | GTTTTTGGATGTCAC[A/G]GGGATTGTGGATACA | 114792 |
| rs577042399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97060025 | TTTGCTTGCAAAAGC[A/G]TGTTGTTCATGTGCA | 114792 |
| rs577042452 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929680 | TCTTCATATTTCTTT[A/T]GTTCTTTCCCTATTT | 114792 |
| rs577051732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97095883 | AAAACAAAACAAAAA[C/T]TCTGAGATTTTGCAG | 114792 |
| rs577070733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028101 | GGAGTGCTGCAAGGC[A/G]GGGAGGACTGACTAC | 114792 |
| rs577080296 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96917525 | CAACAGAAAACAACA[C/G]CTATGACAGAGGCAC | 114792 |
| rs577091821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96932286 | GAAAACATTAATTAC[C/G]TACAATCTGATTTAA | 114792 |
| rs577096365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998848 | ACAGTATTTGAATTA[C/T]GCATTACATGGTAAA | 114792 |
| rs577105171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96933778 | CCAGGGTTAATAAGG[C/T]CTTTTCTTTAGGCAG | 114792 |
| rs577113098 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947135 | TGTTAATAGTAAAAT[A/G]AAACAAACATAACCA | 114792 |
| rs577147837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040346 | TGCATTTGTTTTAAT[C/T]TGTCAAGTTTTTGTC | 114792 |
| rs577173171 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955429 | TCTCTTGTTCTCTTT[G/T]ATCTTGGGGGTTTAT | 114792 |
| rs577188760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96999407 | TCTCAACAACAACAA[C/T]AACAAAGAGTTAATT | 114792 |
| rs577221852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96960509 | GTTTTTCTCTTTAAA[A/G]ATTATAAGGTATTAT | 114792 |
| rs577225077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96992376 | TGTCTCACTCTTCTC[A/G]CTTCTGTGTGGATTG | 114792 |
| rs577273015 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056261 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 114792 |
| rs577296663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96993236 | ATTGTTCTGGTCTGT[C/T]AGCTCAGCTGATCTC | 114792 |
| rs577304297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96961393 | AATTTTTGGTATCTT[A/G]TGTTTATTGATTATA | 114792 |
| rs577310301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96952710 | TTCTATAATCATTTA[C/T]TGCACTGTAGTAAAT | 114792 |
| rs577314947 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075490 | TTAGACTTTATCCTA[A/T]CAACTCTATGACAAT | 114792 |
| rs577326393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96963345 | TTTGTTGTGCAGATT[A/G]AAGTCAGTACCTTCT | 114792 |
| rs577327824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939145 | CCTCTTCCTGCCATT[C/T]TGTCATTGCAGGATG | 114792 |
| rs577334789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97089505 | CTTTTCTGGGTAGGC[A/G]CGGTGGCTTACGCCT | 114792 |
| rs577347524 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96953389 | AATACCAGCACTTTG[G/T]TAGGCTAAGGCAGGA | 114792 |
| rs577350085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97126221 | ATTCATTTTACACCA[A/G]TGTCTAGAACTACAT | 114792 |
| rs577375412 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068208 | ATACATTTTGTATCA[A/C]CTTGCCCAAGCATAT | 114792 |
| rs577403221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082097 | GATTGAGAGTTTGCT[A/G]CTGGAGGCAGGAATG | 114792 |
| rs577410428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96939635 | TTCTAGGAGGAAACA[C/T]AGTGTCAACACAGTG | 114792 |
| rs577431967 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97068733 | TGACAGACTCACATA[A/C]ATGTAATTGCAGGGT | 114792 |
| rs577432670 | snp | A/G | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96977229 | ACATATTATTAAAAT[A/G]ACCATTTTGCATATA | 114792 |
| rs577452009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97020097 | ATAGGTGCCAGCCAC[C/T]GTGCCAGGCTGATTT | 114792 |
| rs577452452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97082401 | GGCGGATCATGAGGT[C/G]AGGAAATCAAGACCA | 114792 |
| rs577464395 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024583 | AGCCATCATCATATT[A/C]TTCTTTAAAATTATT | 114792 |
| rs577493963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96983698 | TGTTCTCTGATGGTA[A/G]TTTGTATTTCTGTGG | 114792 |
| rs577503022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077094 | ATGCACAGCTGGAGA[A/G]AGAAGAGTCAAACAA | 114792 |
| rs577516248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97075901 | AGCTTTTATACCCAA[C/T]AGAATAAAGTAAATA | 114792 |
| rs577532510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96987635 | ACCAAAACAGAGCCT[A/G]CATTGCCAAAACAAT | 114792 |
| rs577541224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014151 | TACAAAAAATTAGCC[A/G]GGCGTTGTGGTGGGC | 114792 |
| rs577558214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97062333 | CATTCTCCTCCTTAG[A/G]CCATGCCTCTTCTGC | 114792 |
| rs577562989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97077619 | AAACCCAGTACCTAG[A/G]TAGCATCGCAAGGGA | 114792 |
| rs577568478 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943823 | AGTCATATCTGGCAG[A/G]GGAACGAGTGTGCAG | 114792 |
| rs577576659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97014871 | TGTGATATGGTTAGG[C/G]TCTGTGTCCCCACCC | 114792 |
| rs577594045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97097252 | TTTCATCAGACTCCT[C/T]CATCACCGAGCTGTC | 114792 |
| rs577613527 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97111217 | TCCTTTCACCTGCAG[C/G]AAAGAGAGAGATGGC | 114792 |
| rs577618724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96919366 | ATGATTAAAGAGAAC[A/G]GGAAAGGGTCAGGAA | 114792 |
| rs577626498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97078302 | CATGTATGCTACTAC[A/G]TCATGGGCATAGAAC | 114792 |
| rs577628474 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922437 | AGAGCTCCTGATATC[C/T]TTCTACTAAGTTCCT | 114792 |
| rs577636352 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96970774 | ATCTTCTTTGCTTAT[A/T]ACTATGACCATTGCT | 114792 |
| rs577683263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96912089 | TCTGAATCTGAACTC[A/T]TCATCTTCCCCCGAC | 114792 |
| rs577683929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96979429 | TTTTCATTGACTTTG[A/T]CAAAGATCAGATGGT | 114792 |
| rs577684067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96985503 | CTTCGTCACTTTCAA[C/G]TATACCAATCAGACG | 114792 |
| rs577721232 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96980198 | GGACTTCCAGTACTA[A/T]GTTGAATAGGAGTGC | 114792 |
| rs577727787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97090990 | GCACATTGGGAGGTT[C/G]AGGCAGGCTGATCGC | 114792 |
| rs577741674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105327 | ACACGCTTTCCTGGC[C/T]TCCTACTTCTTGTTG | 114792 |
| rs577759636 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | KLHL32 | GRCh38.p7 | 6:97069417 | TTTTTTTTTTTTTTT[G/T]GTACCAATGGCAATT | 114792 |
| rs577782634 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97106734 | GGGTGACAGAGGAGA[A/C]CCTGTCTCAAAAAAA | 114792 |
| rs577782841 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050741 | GACGCAGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 114792 |
| rs577802137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:96947610 | ATATATACAGAGATG[A/G]TAATTTGGGAGTACA | 114792 |
| rs577802952 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043199 | TCAGGTATTCCTTTA[A/T]AACAACTCCAAATGG | 114792 |
| rs577806771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97007661 | TGGATGAGGTTTTTT[C/G]CTTTTTCATCTTTGA | 114792 |
| rs577806810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000416 | GGAAGTCTTTCTTGA[A/G]GAAGCATGTAGTAAG | 114792 |
| rs577817246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96994745 | TCAGCCAGATAATAA[A/T]GCTTTAAAAAATAAC | 114792 |
| rs577842375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97107253 | AGCCGAGATCGCGCC[A/G]CTGCAGTCCGGCCTG | 114792 |
| rs577843552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97000987 | GGAAAAGGCAAAACT[A/G]TGGAGACAATAAAAG | 114792 |
| rs577844601 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KLHL32 | GRCh38.p7 | 6:97099662 | CTCTGACTTCTTTGC[A/G]TGACTGCTGCACGCT | 114792 |
| rs577878091 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055625 | CAACATGGTGAAACT[C/G]TGTCTCTACTAAAAA | 114792 |
| rs577896104 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119483 | GGGATATCAAGGTCC[-/A]AAAATATTTCCACTG | 114792 |
| rs577902677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97134877 | AAAAAACTTCGTAGT[C/T]GCATCATTTGTTTTT | 114792 |
| rs577904938 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96988948 | ATCACACACTGGGGC[C/G]TGTTGTGGGGTTGGG | 114792 |
| rs577906221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97100274 | TTAGAGAAGGCAGTG[C/T]AAAATATGCTTTTTC | 114792 |
| rs577928926 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96905691 | ACATTCAAAAACTAT[A/T]AGCTATTATTCTTTT | 114792 |
| rs577934235 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049971 | TGTAGGGCAGGGCCA[A/G]TTCTAAGTGACAGTC | 114792 |
| rs577943681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97136604 | ATAAAGGAGCAGCTG[C/T]GTAAGTGTGCAAGTG | 114792 |
| rs577944905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97035420 | GTATATTTAATTTTG[C/T]CAGTGAGATTTATGT | 114792 |
| rs577949847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97002983 | TCTTTATGGTAGAAA[A/G]TATATATATTCCTAT | 114792 |
| rs577950608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97119958 | AGCTAGAAGACGAAA[C/T]CCAGAGGTGAAGGAG | 114792 |
| rs577958776 | in-del | -/AATC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117098 | GCCCAGCTTATAATA[-/AATC]AATTGTGAATCTAAA | 114792 |
| rs577963059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127220 | CTGGATTGCTTCTGA[A/G]ATGTTTCTTGAAAAT | 114792 |
| rs577992245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96904321 | TACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTTT | 114792 |
| rs577995921 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97011935 | GTTACTTTGTTTAAT[-/C]CCCCCCAATAATCCT | 114792 |
| rs577999898 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896245 | TGGATTTACACATAG[A/G]TTCCCATTCCTAATG | 114792 |
| rs578003419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97112451 | TTTTTCATTGATGAT[C/T]TTTTTTTTTTCCTGA | 114792 |
| rs578004598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022064 | GTTTTGCAGTATCCT[C/G]CTAGTCTGTTTTCCT | 114792 |
| rs578013156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97070889 | TGTAAAAGAAGATCT[G/T]TGTTTCATTTGAGAT | 114792 |
| rs578013477 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97028803 | ATTCAATAAGAAAGC[A/G]TAAAAGTGCCATCCC | 114792 |
| rs578032710 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031239 | TTGAGATATCTTTTA[A/T]ATGTATTATACCCAA | 114792 |
| rs578052139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96971771 | ATCCCTGGGAACTCA[C/T]AGAGTATCCAATAGA | 114792 |
| rs578052919 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931206 | CTAGTTAAATCTATG[-/T]TTTTTTTCTTTTTCT | 114792 |
| rs578104605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97030012 | CATGTCTTTTTACTT[C/T]CATTTAACTCTGTTT | 114792 |
| rs578110326 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956844 | TGTTTCCCCAGTTCT[A/G]ATGTTTCTTGCAGAT | 114792 |
| rs578123282 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96986311 | CCCAGTTAGGCTACT[A/C]AGGGGTCAGGGACCC | 114792 |
| rs578132159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97022780 | CAGCCCTGATCACCT[A/G]ATTTTTAAAGAAGAC | 114792 |
| rs578146890 | snp | C/T | 0 | 0 | intron-variant | KLHL32 | GRCh38.p7 | 6:96913590 | AAGCAGGCTCCAGCA[C/T]ACTGCAGTCTAGATG | 114792 |
| rs578151332 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930858 | GTCAGTCAGTTTCCT[C/T]CTACCCAGGCAGCTC | 114792 |
| rs578167234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KLHL32 | GRCh38.p7 | 6:97056829 | AGATCGTTTGAGCCC[C/T]GGAGCTCGACACCAG | 114792 |
| rs578175723 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138331 | ATTGCTTGAGCCCAG[G/T]AGTTTGAGAGCAGGC | 114792 |
| rs578200829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96928550 | GATTCTTCTAAAGAC[C/T]GAACATAAAGTCAAG | 114792 |
| rs578210444 | snp | C/T | 0.000611284 | 0.0174719 | intron-variant | KLHL32 | GRCh38.p7 | 6:97105551 | ACTTGTGCCTCACAG[C/T]GTGGGATTCTGCAAA | 114792 |
| rs578210745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97043926 | TTCTTGTGATGGCTC[C/T]AGCTTTGTTCTTTTT | 114792 |
| rs578223560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:96995595 | CTGTTTATCCAGTGT[C/T]GTAGCCACACTATTC | 114792 |
| rs578225461 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989588 | CGTCTTGGGGATGGT[C/T]GTCTTGTATAGTATC | 114792 |
| rs578238518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97058057 | TCTTTCATTGACCAT[A/G]TTTATGTGAGTCTGT | 114792 |
| rs578239343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051125 | TAAGGTGCCTGAGGT[C/T]GTATGTACAGATCAT | 114792 |
| rs578254434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KLHL32 | GRCh38.p7 | 6:97051865 | AGAAAAAAAGAACAA[C/T]TGTGCTCCAGCCTTA | 114792 |
| rs745320726 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141797 | CACAGTACCAAACAG[A/G]TGATAACAGATATTC | 114792 |
| rs745339625 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979178 | TTTTTGGTTTTGTTG[C/G]AATTGCTTTTGGTGT | 114792 |
| rs745360272 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022614 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACACC | 114792 |
| rs745409457 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011790 | CAGAAAATGAATACA[C/T]TTCTTACTAAGGAAA | 114792 |
| rs745430411 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012780 | CAATTAAACTATATA[A/T]GAGGGTTCTCATATA | 114792 |
| rs745445941 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967233 | GAATTTACTGTGGTG[A/G]CACAAGGACTAACTG | 114792 |
| rs745462385 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062274 | AATGAGCGCAACTGA[C/T]AGGATTTAAAGGCTA | 114792 |
| rs745462671 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902479 | AATTTGTTTATAGGC[A/G]TTGCATATTGGACCT | 114792 |
| rs745466281 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033282 | CATTCAATATTTGTC[C/T]TTCTGTGTCTAGTTT | 114792 |
| rs745467050 | snp | C/G | 1.6636e-05 | 0.00288405 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976057 | TCACAATGACAGTGT[C/G]CTGGCAGCGCTGAAT | 114792 |
| rs745487543 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105844 | TTAAAAGATTTGATC[A/C]CTCATCTGATGAGAG | 114792 |
| rs745513563 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121126 | TTGTTGATTTACCCT[A/C]ACATCACTGCCCAGG | 114792 |
| rs745536646 | snp | C/T | 3.49101e-05 | 0.00417778 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976165 | CCTAGCAGCATGCAG[C/T]GACTATTTCCGGGTA | 114792 |
| rs745550611 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010566 | GATATTGAAGAATTT[A/T]TCCCTCATGTTTCCT | 114792 |
| rs745574132 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948839 | CCCAAGCCTATTGAC[C/T]GAGCCAAGAAAACAT | 114792 |
| rs745586678 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904095 | CCCGTAATCCCAGCA[C/T]TTTTGGGAGCCTGGG | 114792 |
| rs745590143 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096100 | TCTTCTTTTTACCTT[A/G]TTAGTTATATACCCC | 114792 |
| rs745608501 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132785 | GAAGTTTGTTCAAGT[A/G]GTTCAGCGAGGTTAC | 114792 |
| rs745614352 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943539 | TAATTGGATTCCTCC[A/G]CATTTTGTATGAGAA | 114792 |
| rs745621684 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972791 | TGAGGGAGCTGTTTG[A/C]AAGCATGTGTCTGCT | 114792 |
| rs745623100 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959381 | GACTTGAACAACACA[A/G]ATTTATTTTCTCACA | 114792 |
| rs745635634 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969703 | TGTGCTTCAAACTTA[C/T]CTTTCATATCTTCTC | 114792 |
| rs745641018 | snp | A/G | 6.59435e-05 | 0.00574172 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97127420 | TGGAGTAACTAATAC[A/G]GCACAATATCAGAAC | 114792 |
| rs745669183 | in-del | -/CTAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072552 | TTATTATGAAATGTG[-/CTAT]CTCTTTGGCTTTTTT | 114792 |
| rs745709961 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120033 | TAATAAGGAAAGAGA[A/G]TGAAATTGAAGGTGT | 114792 |
| rs745710437 | in-del | -/GATATTAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950070 | CCAAGATTTTAAAGT[-/GATATTAA]TTTAAAAATTAAAAT | 114792 |
| rs745718635 | in-del | -/GTGAGTGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950612 | GAATGAGTTGAGTGA[-/GTGAGTGA]ATGAGTGAATGAGTG | 114792 |
| rs745722335 | in-del | -/ACT | | | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900126 | TCTCTCTGCCTGAAC[-/ACT]ACTAGCCCTGCTTCC | 114792 |
| rs745726408 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994744 | TTCAGCCAGATAATA[A/G]TGCTTTAAAAAATAA | 114792 |
| rs745728359 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006166 | ATAGGTCTGTAAGAA[C/G]TTGCTTTATGAAGCT | 114792 |
| rs745737291 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061434 | TAAGACATTTTGTCT[C/T]GTCCACTGTTTATGC | 114792 |
| rs745744002 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039878 | AAAATCGCTCGAAGA[G/T]AATAATTTGAATGTT | 114792 |
| rs745754187 | snp | A/G | 0.00026448 | 0.0114965 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130724 | ACATGGAGGTCTCCT[A/G]CTAACAGAATACACT | 114792 |
| rs745762277 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082612 | AGCAAGATTCCATCT[-/A]CAAAAAAAAAAAATA | 114792 |
| rs745763241 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068259 | CATTCTTTATGTGCA[C/G]CAAGTATCATTGTCT | 114792 |
| rs745768993 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935843 | TTTATTTAAATCTCT[A/G]TGCAATAATATGACC | 114792 |
| rs745771032 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100357 | TCAAATTTATGTATA[A/T]CCTTTGCAGCTCACT | 114792 |
| rs745781271 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971592 | GCTCCCTGGCATTAC[C/T]AAAAGGTCATCTTAC | 114792 |
| rs745794734 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907629 | CTTTCACCAGTTTCT[C/T]ACCCCTAAGAGGCCA | 114792 |
| rs745800678 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036914 | GAATCCTCCTGCTCT[C/T]TTCCCCTATGGGGGG | 114792 |
| rs745825615 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967995 | CAAAATATCTTCAGA[A/G]CAAAGAATAAGAGAG | 114792 |
| rs745829736 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131650 | CCCTTCCATGTCTGC[G/T]CAAATAATAGGAAAA | 114792 |
| rs745830412 | snp | G/T | 1.64855e-05 | 0.00287097 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085276 | CTAACGCTTCCCTAT[G/T]GCCTGCTTCAGGAGG | 114792 |
| rs745859726 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909607 | CAGAGATAGGGGAAA[C/T]TTTGCCTAAGATGCT | 114792 |
| rs745862634 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085888 | AAGCCCTGCCTTTTC[A/G]CCTGACATAGCATTC | 114792 |
| rs745865268 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056743 | TAATTCAGGCCATAT[A/G]AAGTTTCTGTCACAG | 114792 |
| rs745881313 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996904 | TTAGGGGCATGAAAA[A/G]TGGTTAAGTAAGAGC | 114792 |
| rs745887284 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927503 | AGAAGCTGCCATTTT[C/G]TCGTGTTTCTCCTAG | 114792 |
| rs745912475 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963222 | CTTGGCCTTATATAC[C/G]ATCCTAGGATTATCA | 114792 |
| rs745951219 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950970 | TTAAACTCAAGAAAG[A/C]CTTGTAATACAAATT | 114792 |
| rs745967464 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899758 | GCTCTTCTTGTCAAA[A/G]CATATAAATTAACAG | 114792 |
| rs745977618 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985906 | TCCAGCTTTGTTCCA[C/T]TGCTGGTGAGGAGCT | 114792 |
| rs745978865 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906803 | TAGTTAATCCTTTTT[A/C]GAGCTTTTGATTCCA | 114792 |
| rs746011884 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997669 | ATCGCTTGAGCCCAG[A/G]TGGAGGCTGTAGTGA | 114792 |
| rs746020162 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059747 | TGTTTCATGTTCCAT[C/G]TGTGAGAATTCTGTC | 114792 |
| rs746020189 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025299 | CCATCTGATGTTGAC[G/T]GCATTCTGGGCTTGC | 114792 |
| rs746021993 | in-del | -/CCTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930990 | CCTGGCGGGTACAGA[-/CCTC]CTAGCCTTTCTGCAA | 114792 |
| rs746044221 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075504 | ATCAACTCTATGACA[A/G]TGTTGAGAAAATTCA | 114792 |
| rs746054529 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975319 | ACATAGAAACTAAAT[C/G]CTGATAATAGATAAA | 114792 |
| rs746069103 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921657 | ATGACAATTTCCTCC[C/T]TACTTGCTTCGGGAG | 114792 |
| rs746112818 | snp | A/G | 1.67136e-05 | 0.00289076 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064637 | AAACAGATTTTGCTG[A/G]AGCCAGGTGTGATCC | 114792 |
| rs746113836 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982949 | AGAGAGGGCATCCCT[A/G]TCTTGTGCCAGTTTT | 114792 |
| rs746116913 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137515 | CCCATTTCCTGTAAA[A/T]TAATGCGTTGTTGAA | 114792 |
| rs746125262 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933079 | TGGTTAAGGGTTTAG[C/T]GGTTAAGGATTTCAC | 114792 |
| rs746127889 | in-del | -/AG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098572 | GTTTTTTAATAGTAA[-/AG]AGAGTCATTAGGTGA | 114792 |
| rs746133545 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047673 | GGTATGAGGAAGAAG[A/G]AAGAGAAATACTCTG | 114792 |
| rs746146992 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090534 | AAACAAAAAGCTACT[A/G]TCCCTTTACAGTTGG | 114792 |
| rs746151106 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075546 | ACATGCACAATAAAC[A/G]TGATAACTTCTTTCC | 114792 |
| rs746176917 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115365 | AATGGTAGTTACTTG[A/T]GCCATTCTAACCCTT | 114792 |
| rs746211704 | snp | C/T | 1.6525e-05 | 0.00287441 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896785 | AATCAACATACACAT[C/T]TTTTAGAAACGACAG | 114792 |
| rs746216155 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912839 | TCCTCTGCATTGTAA[C/T]TGCTGCTTATTTGTC | 114792 |
| rs746221934 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064953 | CTGTCCTGCCCACCT[C/T]AGGTCCCCACGACCA | 114792 |
| rs746242318 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029800 | TGTAACCAAAATGTA[A/G]TAAAGGCTAATAACC | 114792 |
| rs746248286 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070613 | ACTGTATCTTCGTTT[A/G]TGAGGATTTTAAAGA | 114792 |
| rs746256219 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058944 | CACAAGCATTCTTTT[C/G]GTCCTTAAAACAGTT | 114792 |
| rs746259707 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018619 | AAAAAAAAAAAATCA[A/C]TCCAAGTATATTTAT | 114792 |
| rs746286451 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067173 | GTGGAAGCTCCCTGA[A/G]CCTCACCATCCTGCA | 114792 |
| rs746291027 | snp | C/T | 1.68117e-05 | 0.00289923 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896894 | ATCAAGGAAAATTTC[C/T]TGTAATATCCTAAAC | 114792 |
| rs746300777 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129957 | GTGCCTAGAAATAAC[C/G]TTTCCCAATTTGGCA | 114792 |
| rs746304445 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923400 | AAATTCTTAGGATGA[C/T]ACTGCACCTAATGTT | 114792 |
| rs746333418 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968071 | TTAAGTAATGAGACC[A/G]GCTTCTTTCCATGAC | 114792 |
| rs746334774 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052121 | ATGTAAAAGAACAAA[C/T]GAAAGAAGTTTGTGT | 114792 |
| rs746336812 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039464 | GTTTAATAGAAGAAA[G/T]AAGAGCTAGTGTTAG | 114792 |
| rs746346135 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115216 | AGGCAGGGTTTCACT[A/G]CATTGCCCAGGCTGC | 114792 |
| rs746347697 | snp | A/G | 0.000186626 | 0.00965806 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114557 | CACACTTTCATTGTG[A/G]TATATATTTAAAAGT | 114792 |
| rs746352275 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955652 | TGATAAAGACATACC[C/T]GAGGCCAGGCACGGT | 114792 |
| rs746362478 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128704 | ACCTCTGCTTCCCCA[C/G]CACTGATTAGTATTC | 114792 |
| rs746378331 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028541 | CTGTTCTCTAAATAA[A/G]TTTCCTTTTTTCATA | 114792 |
| rs746388136 | in-del | -/TTAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033874 | TTAAAATTCAGTTAT[-/TTAA]TTATTTATTTATTTT | 114792 |
| rs746389902 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040556 | AGTTTCAGTAAATCT[G/T]CATTGGGGCCCTGAG | 114792 |
| rs746413128 | snp | A/G | 1.65655e-05 | 0.00287793 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113803 | TGTGAGGTGGTTGGA[A/G]CACAACTGCCACTAC | 114792 |
| rs746420622 | snp | C/T | 1.65466e-05 | 0.00287628 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132778 | TCCTTTTGAAGTTTG[C/T]TCAAGTGGTTCAGCG | 114792 |
| rs746421557 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911946 | CTGCACCCTCTCTCT[C/G]AGTAATCTCTTCCTG | 114792 |
| rs746435744 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065269 | GAGAAGGAGGGAGAG[-/A]AAACCCCCGAACACC | 114792 |
| rs746501968 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061734 | GAGATCCCTTTTTTT[-/C]CTGCAGAGGTTGTTC | 114792 |
| rs746520576 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019602 | CTCAGCAGCTAGGAA[C/T]GAAGAATTCTTCATT | 114792 |
| rs746523558 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106612 | GCTGGGTGGTAATGG[C/T]GCACGCTTGTAATCC | 114792 |
| rs746541833 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139985 | GAGGATTAGGCGAAC[A/C]CTTTGTAATACTTTG | 114792 |
| rs746546665 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091869 | GCTGTGTTCATGTTT[C/T]AATATTTGGACCTTG | 114792 |
| rs746554058 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021242 | GTAAATTGTGTGTCA[C/T]TGATGTTTGCTGTAT | 114792 |
| rs746554694 | in-del | -/TAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023851 | GTAACTCTCTGGAGA[-/TAT]TAGAATCTGGTTCAG | 114792 |
| rs746572926 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123804 | GGGGACAGTATAGCA[G/T]CATGTGGCATCGTAA | 114792 |
| rs746583657 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009588 | TGTATATTGTGAAAG[G/T]GAGGATTTGTACATG | 114792 |
| rs746591401 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928566 | GAACATAAAGTCAAG[A/G]GACAAACCAAGTATT | 114792 |
| rs746593713 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914291 | GTCTTGTTTCAAGCC[A/T]CTGTACTTGAGATAA | 114792 |
| rs746621090 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086063 | GAGCCTATCTTCCTC[C/T]TCCATATTACAGCCT | 114792 |
| rs746623732 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071641 | CCTCCTCATCCTCCC[G/T]GTCTTTGTTAAGGGA | 114792 |
| rs746642719 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136669 | TCTTCATTTACTATT[-/A]TTTTTTTTGGCTGGA | 114792 |
| rs746651484 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085386 | CACTGAAAAAGCATG[C/T]CGTGATTGGAAGTTA | 114792 |
| rs746655791 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959192 | TCAGGCCCCAGGAGG[A/C]CTCCAACGTCATGGA | 114792 |
| rs746666368 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994415 | CTATACAAATTATTT[A/G]TGTTTTTTTTCCTTT | 114792 |
| rs746690390 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135468 | GTGCCACCATGCCCA[-/G]CTAATTTTTTGTATT | 114792 |
| rs746698386 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919257 | CCAGTAATGAGGTTA[C/T]CAATAATCAATTTCA | 114792 |
| rs746699432 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900685 | TTGAACATAATTCAA[C/T]AGCATTCTGCGTTCT | 114792 |
| rs746703903 | snp | A/G | 3.53051e-05 | 0.00420135 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130742 | AACAGAATACACTTA[A/G]ATTTCTTTTTTCAGA | 114792 |
| rs746724547 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936554 | CTCTACCTTCAAAGT[A/G]TACCCAGAATCTGAC | 114792 |
| rs746744797 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098407 | TTCAGCAGCATATTT[C/T]TACCTAGCCTGGGAC | 114792 |
| rs746747191 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072416 | TTTGATTGATTTTTT[A/G/T]AAAAAATCACAACCT | 114792 |
| rs746768059 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130185 | TATTGAACATTTTTC[A/G]TGTGCATTTTTCTAA | 114792 |
| rs746776116 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969998 | ATCAAGTTGTATAAG[C/T]CAGAAATATAGGTGT | 114792 |
| rs746791110 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971314 | CAAAATTCTTTCCAT[A/G]AACATCAAACCCTAT | 114792 |
| rs746795768 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130847 | TATGTTCTTGGAGGC[A/G]ATGACCTAGACTACA | 114792 |
| rs746813491 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958414 | TAGGGGTTAACCAGG[C/G]AAAAAGGAGGGGTAG | 114792 |
| rs746822443 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927131 | ATAAAAGACCATGAA[A/G]TGCTCTAAAATAGGA | 114792 |
| rs746863005 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043773 | GATATCTCACCATAG[G/T]TTTAATTTGCATTTC | 114792 |
| rs746880694 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992377 | GTCTCACTCTTCTCA[C/T]TTCTGTGTGGATTGT | 114792 |
| rs746885368 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098354 | TTTTGCCTTTTTTTA[A/T]TTGTTGTCTTCATTA | 114792 |
| rs746896957 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024267 | TTCGATAAGCATTAA[C/T]TGCCTGGCTGACTAT | 114792 |
| rs746902721 | snp | C/T | 1.80029e-05 | 0.00300019 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085392 | AAAAGCATGCCGTGA[C/T]TGGAAGTTAAAGGAC | 114792 |
| rs746917217 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065611 | ATTATAGCATTAAAA[A/T]ATTAATTTGAAGAAA | 114792 |
| rs746939527 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982572 | ATATTGACATGTGTG[G/T]TTCTCCTTGAAGAGG | 114792 |
| rs746957744 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025344 | GAAAGATTGAATTAT[C/T]AGTATGCTTCTCACT | 114792 |
| rs746961082 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067245 | AGGAAAGGGATACCT[G/T]GCACTGTGTGGGCTC | 114792 |
| rs746977569 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125962 | AGAAAGAAGTTATGA[C/T]TACAAGTTTTCTAAA | 114792 |
| rs746995133 | snp | A/T | 1.64773e-05 | 0.00287026 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897847 | GCCGCACGTGGGAAC[A/T]CCGGCGCAGGACAAC | 114792 |
| rs747001437 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950230 | TTCTACATTTGTGTT[-/A]AAAAAAAAAAACCAT | 114792 |
| rs747022052 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961879 | CCCAACCTGTGCAAC[C/T]AACTTGTGAAGTTGA | 114792 |
| rs747033798 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053608 | CTTTCTGCTTTCTTC[A/G]GATGCCCATTTTCTT | 114792 |
| rs747034319 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046575 | CACAGAGTAGAAGTT[G/T]ATACCTCTACAGCCT | 114792 |
| rs747068604 | in-del | -/TAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044810 | GTGTATAATTATTCA[-/TAG]TAGTCTCTTATGGTC | 114792 |
| rs747075689 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006572 | TAGCTGGTTACTATG[A/C]AGACTTGATTGTGTA | 114792 |
| rs747116208 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017860 | AGATGGAATGGCAGC[A/G]GAGGACCTAGAGGAA | 114792 |
| rs747123497 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931433 | GAAGTTAGCCTGAGC[A/C]GTATATTGTAGGATC | 114792 |
| rs747129139 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007708 | ATTGTGCTATAAGGT[A/G]GGTACAGTCAACTGG | 114792 |
| rs747137312 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121752 | GGTCTAGTAAAAGAC[A/G]GTAAACTAAATGGTG | 114792 |
| rs747140579 | snp | A/T | 1.65669e-05 | 0.00287805 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064751 | CTTGCATCCTGCTCA[A/T]ACACCCTTCACATTC | 114792 |
| rs747182209 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069658 | CCCTCCCTTCACATC[A/G]TGGGAGTTCATTATG | 114792 |
| rs747197133 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962195 | TTCAGGTTTGACTTC[-/A]AAAAAACCCAAGTGA | 114792 |
| rs747197297 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911546 | CCTCTACCTTCTACC[C/T]CGAATCTCTTCCCCT | 114792 |
| rs747199039 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102282 | TTTCAGCTGACTTCA[C/T]CCTGGTAATGCATCC | 114792 |
| rs747209298 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990503 | CTCTGAAAGTGTAGT[C/T]TCTTCTCCCAGTCAA | 114792 |
| rs747227097 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008280 | GTGCAGTCTGCCAGC[A/G]AAGGAGCTATGGTAA | 114792 |
| rs747232313 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973405 | TTCTTCGGTTCCACT[A/G]CAAATGAAATTTTGA | 114792 |
| rs747245252 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942427 | TAGCTCTACCATGCA[A/G]TAATTTCCCTTGTTC | 114792 |
| rs747249803 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989087 | GTGCACATGTACCCT[-/A]AAAATTTAAAGTATA | 114792 |
| rs747250867 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941358 | CTAGGAAGTGGTGAA[A/G]CAAACATGCATTTTG | 114792 |
| rs747251417 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088142 | TATTTAGAGGTAACA[G/T]AGAGAGTTGTTCACA | 114792 |
| rs747262076 | snp | C/T | 6.73004e-05 | 0.00580049 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897626 | GGGCAGCACAGGGAC[C/T]CCGCGCCCCCGGGCC | 114792 |
| rs747282817 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930705 | TTTAGTGATGCAGTA[A/C]GCTGCTTAGATGGGC | 114792 |
| rs747283257 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113074 | CTCCTCTATATTCTG[-/T]TTTTGTGCAAACGAC | 114792 |
| rs747283456 | snp | A/T | 1.6908e-05 | 0.00290753 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085109 | ATCTTTTTTCATTTT[A/T]ATTTTTTGGCACCCA | 114792 |
| rs747296400 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954450 | AGGCTTGTTATGCAG[C/T]GATTACCCCATAAAG | 114792 |
| rs747307391 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130002 | TAATATATTAAAGGA[A/C/G]GCTGATAAAAGGAAA | 114792 |
| rs747315821 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917302 | TCCTTGCTTTCCATC[A/C]TCCCTGATCTCTCTG | 114792 |
| rs747332446 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127595 | AGAGAAAAGGAAGCA[A/T]CTGAATAAACTGCTT | 114792 |
| rs747350041 | snp | A/C/G | 3.29572e-05 | 0.00405928 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897718 | GTGTCTGGGAGCGAC[A/C/G]GAGGGCTTCATCTTG | 114792 |
| rs747386462 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068538 | AGTAAAAAAGTCATT[A/T]TTCACACCACACTGG | 114792 |
| rs747396508 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048573 | TTGTTTTTTTGATTG[C/T]CATTTGGTTCCCTAA | 114792 |
| rs747409251 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910980 | GTATGGTAAAATGAA[C/T]ATAGTTAATTGTGTA | 114792 |
| rs747418150 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955538 | AATGTTTCCTTAAAT[C/T]AGGGTGTGAGTTGCA | 114792 |
| rs747421697 | in-del | -/A | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923474 | CCAGGACTGCTAGAT[-/A]AAGTAGGTACCCAGC | 114792 |
| rs747430069 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103431 | TGTTAGCCAGGATGG[C/T]CTCGATCTCCTGACC | 114792 |
| rs747433575 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077748 | AGCTATTATTTCCTC[-/T]TTTCATGTAAAGTCA | 114792 |
| rs747450301 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113918 | CTTGTCCAAGCAAGT[A/G]AGACTGCAACAGCCC | 114792 |
| rs747461675 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126184 | GCTGCTTCTTTGTGA[C/T]ACTGATTAAAATAAG | 114792 |
| rs747474432 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067442 | TTAATGCTAATTGAT[-/G]GGGGGGGTGCCTTTC | 114792 |
| rs747480226 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060088 | TTGTCTGATTTTAAC[-/AT]GCTCAAATCCTTCAG | 114792 |
| rs747481270 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018629 | AATCAATCCAAGTAT[A/C]TTTATTAATAAAGAA | 114792 |
| rs747498382 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010873 | ACTGAGTATTTTGGA[C/T]AGCATATTAGAAATT | 114792 |
| rs747498809 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966125 | CATAAGCACTTTCCT[C/T]CTGTTATTGCTTTCC | 114792 |
| rs747508416 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935006 | TAGGCATTTTGAAGA[A/G]ATATGCAATTGTTAA | 114792 |
| rs747518881 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921826 | AACTCACAGCACTAG[A/G]TTTATGCTACCCTCC | 114792 |
| rs747535020 | snp | A/G | 6.63956e-05 | 0.00576137 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976066 | CAGTGTCCTGGCAGC[A/G]CTGAATCAGCAGAGG | 114792 |
| rs747549590 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131161 | TCAGGGCCTATATTA[C/T]TACCATTATGCACAT | 114792 |
| rs747575325 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000192 | AGGACTCAGGAAAAT[C/T]CAACAAAGTGGTACT | 114792 |
| rs747620028 | in-del | -/TAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941543 | TCTGAGAAGCATTGA[-/TAT]TATTAAGCAGAAGAG | 114792 |
| rs747626642 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898557 | TACTTTCCCTTATCT[C/T]ATTTTTGCTACTAAT | 114792 |
| rs747635380 | in-del | -/TTTTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135300 | AGACAAATTTGTTAA[-/TTTTTT]TTTTTTTTTTTTTTT | 114792 |
| rs747648130 | snp | A/C | 3.36615e-05 | 0.00410239 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130758 | ATTTCTTTTTTCAGA[A/C]TAAGTGGATAAGCCG | 114792 |
| rs747650636 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973922 | AGATGGGGTTTCACC[A/G]TATTGGCCAGGCTGG | 114792 |
| rs747661119 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030536 | ACAAATGAGCTGTGA[A/T]GACTGTAAATCTCAG | 114792 |
| rs747662913 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914028 | GTGGAAGAGAGAGGC[A/G]AAAAGGGAGAACAGA | 114792 |
| rs747671900 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959052 | GGTGTTGAAAGCAAC[C/T]TCCCAGAGAAAATTT | 114792 |
| rs747678636 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104258 | ATATCTGGAACTTAC[A/G]TGTGGCAGGTCTGAG | 114792 |
| rs747690179 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925638 | TTATTTTAAATTAAA[A/G]GCAGATGATTTAATT | 114792 |
| rs747716332 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045953 | AGCCAAATGAGATGA[A/C]AATATATCTGGTGTA | 114792 |
| rs747722489 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896395 | TACCTCAATCCACAG[-/AAA]AAGAATGAGAAAATA | 114792 |
| rs747737526 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938809 | CCCTGCAGTATAATC[A/G]TGTGACCCACATGCA | 114792 |
| rs747747421 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996076 | CCCCTCTGACAGTGG[A/G]TACACATAAGTTACA | 114792 |
| rs747767274 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969728 | CTTCTCAGCAACCTT[C/T]GAGTGTTGCTTGTTT | 114792 |
| rs747767720 | in-del | -/CTAAA | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141009 | AATGGTTTAAGCCAT[-/CTAAA]CTAAATTTTAAAAAT | 114792 |
| rs747782142 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124106 | TTTTAAAATGTATCT[C/T]AGTATTGAGAGAAAA | 114792 |
| rs747790389 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002573 | GATTATTTCATTACT[C/T]AGGTCCTAAGCGTAG | 114792 |
| rs747800967 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016775 | CTCGAATTGCAATCC[C/G]CATAATCCTGGGAGG | 114792 |
| rs747811815 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098142 | GTATAGGCTAAAAAC[A/G]ATACAGACATCTAAT | 114792 |
| rs747823371 | snp | A/G | 0.000121278 | 0.00778617 | intron-variant, missense, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105456 | AGAAGTGTGGAATTT[A/G]TGCTGCCTTTTGTGC | 114792 |
| rs747826015 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130095 | GGAAAGAACAGCAAA[A/G]CCATTACCCTAGCTT | 114792 |
| rs747829030 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997625 | GCATGCACCTGCAGT[C/T]TCAGTTTCTTGAGAG | 114792 |
| rs747846651 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997484 | CAGGCATGGTGGCTC[A/G]TAAATGTAATCCCAG | 114792 |
| rs747860862 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083856 | CCTTCCCCCATCACG[C/T]TAATGGAAAATTTAA | 114792 |
| rs747860881 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070767 | TTCTTAAAAATGAAG[C/T]GTTTCCAGGATTTTA | 114792 |
| rs747893443 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926912 | TGGCCTGCTAGTTAG[C/T]AACCCATAATTACTG | 114792 |
| rs747902963 | in-del | -/T | 1.66751e-05 | 0.00288744 | frameshift-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976117 | CATCACCCTGATTGC[-/T]GAGGAACAGAAATTC | 114792 |
| rs747911901 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981019 | GGGCGGGGGGGCAGG[C/T]GGGGGAAAAGCCCCT | 114792 |
| rs747912506 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082373 | AATCCCAGCACTTTG[G/T]GAGGCCGAGGCGGGC | 114792 |
| rs747929907 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024084 | TGTGTCTGATGATTA[A/G]TCATTTAGGTAGTAT | 114792 |
| rs747932450 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081589 | CTCTTCCTTCAACTC[A/T]CAGCATCAAACGGCT | 114792 |
| rs747935193 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142536 | TAGGTAAAAGATCAG[-/T]TTTTTTGGAAAATAA | 114792 |
| rs747950019 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982385 | ACCCTGCTTTTTTCC[A/G]TTTTCTGTTTGCTTG | 114792 |
| rs747972541 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027839 | AACATTTTATGACTC[C/T]GAGAATTCAGATTAG | 114792 |
| rs748021080 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917793 | AAGGAGCATCTTTAG[C/T]GTAAGGACATCAAAG | 114792 |
| rs748037557 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034874 | TTGTTAAACTCATTT[A/G]TTAGTTCTAACATTG | 114792 |
| rs748054219 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949389 | TTGTTCACACTTGTT[A/G]TCATTGTTCATTTAC | 114792 |
| rs748056980 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079257 | CAAAGGCCATGGCCA[C/G]TCTGCTGCAGATGAG | 114792 |
| rs748065603 | snp | A/G | 3.33256e-05 | 0.00408187 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967102 | TGCCCTGTAGGATAT[A/G]TCCTCACATGCCGTA | 114792 |
| rs748085696 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949240 | AGTAGGAATTAATAA[C/G]TTTTCAAATGGATGA | 114792 |
| rs748088798 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023182 | ATCAACTATATTCAT[A/G]TATTACTAAATACAT | 114792 |
| rs748095206 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123102 | TTACTCTATTTACCA[A/G]CAGAGGTATTTTTTG | 114792 |
| rs748108791 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108730 | AAAAATGCAGAGTGT[A/T]TCTATGGCTTACTTT | 114792 |
| rs748109863 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989322 | CCTTAGCATTTGCTT[A/G]TCTGAAAAGGATTTT | 114792 |
| rs748115602 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100672 | GGGATCTGACTGTCC[C/T]TATGTCAGTGACCTG | 114792 |
| rs748127902 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96941830 | AATTTGGAACACTTT[A/C]CTCTGACCTCTTACT | 114792 |
| rs748172952 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015743 | AATTGCCAAGACCAT[A/G]GGGAAAATGTCCCCA | 114792 |
| rs748205628 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086341 | TGATTATTTTCCTGA[C/T]GCCTTTCTGCCTTAT | 114792 |
| rs748207321 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056837 | TGAGCCCCGGAGCTC[A/G]ACACCAGGCTGGGCA | 114792 |
| rs748220695 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96982170 | AAGTCTCCCAGTATT[A/G]TTATGTGGTTATTTA | 114792 |
| rs748225675 | snp | C/T | 1.66843e-05 | 0.00288823 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085129 | TTTGGCACCCAGGAA[C/T]TAAATAGCTTTAATT | 114792 |
| rs748236228 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973075 | TCTGCTTTTAAGGAT[A/C]CCTAACATATTGGTT | 114792 |
| rs748252377 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940925 | CATCACTAACACAGG[C/T]ACAAATTGTTGGAAT | 114792 |
| rs748252420 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929154 | TCAGCACAAGGTAAC[A/G]GGATGAAATAAAATA | 114792 |
| rs748262976 | snp | C/T | 1.64779e-05 | 0.00287031 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897724 | GGGAGCGACAGAGGG[C/T]TTCATCTTGCTGATT | 114792 |
| rs748266807 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079415 | ATGTCCTAACTGCTC[A/G]ATAATTGCCTTGCAA | 114792 |
| rs748272634 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020702 | TAATCAGTTTCCAGT[C/T]CTCATTTTCCTCAAC | 114792 |
| rs748302344 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901332 | CTCCTGGATGCCTTT[-/T]TTTTTTTTTTACTTT | 114792 |
| rs748307063 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016356 | GAGCCCACCTCTTGC[A/C]TCAGTGTGCCTTAGA | 114792 |
| rs748320574 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909149 | TTAAGTTATCAGACA[A/G]GAGGGATACCAATTG | 114792 |
| rs748322542 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050442 | GGTATGGCTGGCTTT[A/G]GCTTTTATTGTGGGG | 114792 |
| rs748329192 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095246 | TGGACCTGCTGAGGA[C/T]TGTAATCAATTTCTC | 114792 |
| rs748347769 | in-del | -/CTTAT | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898550 | TTAGTTATACTTTCC[-/CTTAT]CTTATTTTTGCTACT | 114792 |
| rs748351760 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067717 | TCAGAACTAGGATGT[C/T]GATCTGGCTTGAAAA | 114792 |
| rs748356853 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068367 | TGAATACGCAACTCC[A/C]TTTTTGATAGGAATA | 114792 |
| rs748395338 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000205 | ATTCAACAAAGTGGT[A/G]CTATTAGAGAGTTGG | 114792 |
| rs748405418 | in-del | -/ATAAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117906 | TAGTGCTTTAAAACT[-/ATAAAA]ATAAGACAAATGTTA | 114792 |
| rs748412020 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964711 | CAAATTTTAATTCAA[C/T]ATATACATTTTAATC | 114792 |
| rs748435560 | snp | C/T | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897790 | GATACCGCGAATCAC[C/T]AGTGCTCCCATCTCC | 114792 |
| rs748448516 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106400 | TTATCTGTTCTGTAT[A/G]TTTTTGGGTCAAATT | 114792 |
| rs748469064 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125053 | CAGAGAAGACTTTCT[C/T]TGAGGGCAGGAGGCT | 114792 |
| rs748507264 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139805 | TTATTCAAGGTGATA[C/T]GAATAATAATAGACA | 114792 |
| rs748521738 | in-del | -/TAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126202 | TGATTAAAATAAGAA[-/TAT]TATTCATTTTACACC | 114792 |
| rs748521886 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083948 | TGGTTTTGCTTAAGA[A/C]TCACAAAGCCCATCT | 114792 |
| rs748550059 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078504 | TATTACCCGGAAAAA[C/T]CTGTAATCCTATTCA | 114792 |
| rs748553375 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031688 | AAGTGGAAGTTCTGT[A/G]TTTATAGAAGTGGTG | 114792 |
| rs748554694 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010729 | CTACCTAGGGAAGGA[A/G]ATAGTGGCTTTTGGG | 114792 |
| rs748557585 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920648 | CATTATACCTATTGA[C/T]CTTCCACTTGCATTT | 114792 |
| rs748591535 | snp | C/G | 1.88145e-05 | 0.00306707 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976218 | TAAAATATTGATAAA[C/G]AGAGGATGACAATGT | 114792 |
| rs748598432 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945537 | TGTCCCTTCACCCAA[A/G]CCTACTCAGACTCAA | 114792 |
| rs748603673 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900457 | TAAAAAATGCTAAAT[C/T]TGATTTTTATTTGCT | 114792 |
| rs748603995 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018651 | AATAAAGAAATGTAC[C/T]TCAGAAAAAATATTA | 114792 |
| rs748607518 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927856 | TTCAGAGCAAACACA[-/C]TGCTCCTGGCAGCGT | 114792 |
| rs748614565 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138353 | AGAGCAGGCTGCACA[A/G]CATGGCGAGAGCCCA | 114792 |
| rs748631616 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105113 | AACTGTATGTAATAT[C/T]AAAAGGATAACATGC | 114792 |
| rs748638209 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071804 | GTCATTGACGTCATT[C/T]GGGTTGGGACTATTT | 114792 |
| rs748643613 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976987 | TCAGTACATGCATGC[A/G]GCTAATGAAGACACA | 114792 |
| rs748713775 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133003 | ATTGGAAACTGGGAA[A/G]CTGGGATAGCGTTCC | 114792 |
| rs748737385 | snp | A/G | 0.000121219 | 0.00778428 | intron-variant, missense, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105495 | GAGACTGGTGCCCTG[A/G]CTTACCTCAATGGGA | 114792 |
| rs748752416 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061866 | CTGGAAAAATATATT[C/T]GAACAGTCAGTCACC | 114792 |
| rs748811400 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081879 | GCACATGGTGTGAAT[G/T]TGTAGGTTGTTGTCA | 114792 |
| rs748811634 | in-del | -/T | 3.34387e-05 | 0.00408879 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967011 | TGGAATGCTTGCTGA[-/T]TTCCTCTGCACACTT | 114792 |
| rs748812039 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969498 | GCATTTGCTTGAGAA[A/G]ACCCCAATCCAGATG | 114792 |
| rs748814700 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105247 | ATTAGAAGATAAAGA[A/G]CATGCTCGATACTCT | 114792 |
| rs748819739 | snp | G/T | 1.66882e-05 | 0.00288857 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132628 | ATGGATTTTTTTTCT[G/T]TTTATTCAATTCTCT | 114792 |
| rs748834172 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956786 | GTGTATTAGCACATG[C/T]ACATACATACGCCTA | 114792 |
| rs748835107 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046368 | TTCAAGTCTGTTGTT[C/T]GTTTTTTATTATAAT | 114792 |
| rs748843221 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906202 | CTAAACAGGGAACCC[A/G]GTTAAGCCTGCTTTG | 114792 |
| rs748846891 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029638 | CAGGTGGATTGGGTT[A/G]TTTTTTTCATTTGCA | 114792 |
| rs748849917 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002526 | AGGTTTGTTATATAG[G/T]TAAATTGTGCGTCAT | 114792 |
| rs748865027 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925380 | ATATACACTGAGGAC[C/G]TTTCGTAATTTGGCA | 114792 |
| rs748886207 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936859 | GTTGGTAATACCCTC[A/G]GCCTGGAATGCCCTG | 114792 |
| rs748894738 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949750 | TTCCGAAAGCAGAAC[-/T]TTTCTCTCTTTTTTT | 114792 |
| rs748904011 | snp | C/T | 6.77955e-05 | 0.00582178 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113771 | CTCTCATCTCACTTC[C/T]CTCTGTTTCAGCTAG | 114792 |
| rs748907168 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064379 | AATAAGTGGTTAAGT[G/T]CAGAGCTTCACACAC | 114792 |
| rs748916882 | snp | G/T | 1.64741e-05 | 0.00286998 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113875 | AATGGATGTGGATAC[G/T]CTCCATACAGTTGCC | 114792 |
| rs748933998 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974162 | TACCTGCCTCATGGT[A/G]TTGTTGTGCAGATTA | 114792 |
| rs748937679 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923846 | AAGGTTTTCAATTCG[A/G]TGGTGGAATACTTAC | 114792 |
| rs748966147 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121620 | TGGCCTTTAAAATTG[A/G]TGTTGTAAAGTTTTG | 114792 |
| rs748972652 | snp | C/T | 1.66905e-05 | 0.00288876 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967114 | TATGTCCTCACATGC[C/T]GTAGTGAGCCCTGAA | 114792 |
| rs748976645 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103026 | TATATTTACCTCTAC[A/G]AGGTAAATAAATATA | 114792 |
| rs748979018 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012051 | CTGAATGCTAGAGTC[C/T]AAACCCTAGCCTAGG | 114792 |
| rs748984768 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995791 | CACCCTCTGCCACCG[C/T]GTTAAGTTCATATGT | 114792 |
| rs748994924 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965401 | GTAAAAGAGAATTTC[A/G]TCTATCTTATTATTT | 114792 |
| rs748996024 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096943 | AAACAGCACTGAGAG[G/T]TTAGGTCATTGGAAG | 114792 |
| rs748996218 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081347 | ACAGAGGACTATTGC[A/C]TCCTGGAGTGTAGAA | 114792 |
| rs748999770 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129746 | AATCAGCCAGGTTTG[A/G]TGGCACTTGCCTGTA | 114792 |
| rs749002989 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917680 | GGGTTTGTCAGGAAG[A/G]CTGCTGAGTGTGGTT | 114792 |
| rs749016615 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118319 | TGTTTTACTTACATC[G/T]TGAGAATTGTAGACA | 114792 |
| rs749028871 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995657 | TGCACTTCTCAGCTT[C/T]GCTAGTGACCATTCT | 114792 |
| rs749033748 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034523 | TCATTTGATTTTAGC[A/T]TTTTTTTTTCTATTT | 114792 |
| rs749050520 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961739 | GGCTTCTGCACAAGG[G/T]TAATTGAGCTGTATG | 114792 |
| rs749062658 | snp | C/T | 1.68889e-05 | 0.00290588 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976036 | GAGGCTCTGCCACTC[C/T]GAATCTCACAATGAC | 114792 |
| rs749069383 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947516 | CACTGTGTGATTAAT[A/G]TCATGAGCAATGTCT | 114792 |
| rs749104824 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074838 | TTAAAACCCTAGTTG[C/T]TCAGATAAACTATTT | 114792 |
| rs749106842 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063091 | ATAAAAACAGTGACA[C/T]GATTTCATTTGTGGT | 114792 |
| rs749140399 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120250 | TATGGGTGTGAACCT[A/C]GGTAAGCTCACAGGT | 114792 |
| rs749150689 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979655 | GGGCTCTTTTATGGT[C/T]CCATATGAATTTTAG | 114792 |
| rs749163169 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954059 | TATCACCTGAGAATT[C/T]CTATCATCTCTTTCT | 114792 |
| rs749167204 | in-del | -/AAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904341 | AGCAAGACTTTGTCA[-/AAA]AAAAAAAAAAAAAAA | 114792 |
| rs749189977 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056854 | CACCAGGCTGGGCAA[C/T]ATAGCAAGACCCTGT | 114792 |
| rs749198702 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082771 | GATGTGGGTCAGTCA[C/T]ATAGATGTGGAAGGC | 114792 |
| rs749218931 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974070 | GAATTACATTGTTAT[A/G]TTCTTGGTGATAGGT | 114792 |
| rs749220241 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97010021 | GAAGACTTCTGTTTA[A/G]CCTCACACAGAGGAA | 114792 |
| rs749223191 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087777 | GGTGAAAGGTCTAAT[A/T]TTCATTATTCACCAG | 114792 |
| rs749229520 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931519 | TTAAATAAAATACTT[C/T]TTCTTGTGCTAAATG | 114792 |
| rs749240502 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046232 | AACTAATCTTTAAAA[C/T]AGCTCTAAGGAATGC | 114792 |
| rs749254187 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933930 | GTGGAATCAGTTTCC[C/T]TGAGTTTTCACTCTG | 114792 |
| rs749273370 | snp | A/C | 1.64947e-05 | 0.00287177 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127397 | AACACATGTTAATCC[A/C]TTACAGGTGGAGTAA | 114792 |
| rs749298964 | snp | C/T | 1.6596e-05 | 0.00288058 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064756 | ATCCTGCTCATACAC[C/T]CTTCACATTCCTTTC | 114792 |
| rs749322397 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952584 | ACTCCCTAAAACTGA[C/T]GCTTCCTTGTTCAGG | 114792 |
| rs749336430 | snp | A/C/T | 4.94208e-05 | 0.00497075 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897793 | ACCGCGAATCACTAG[A/C/T]GCTCCCATCTCCTCA | 114792 |
| rs749365627 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004079 | TTTGGGAAGTATGGC[C/T]ATTTAACAATATTGA | 114792 |
| rs749374020 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014560 | AGGCACTACTACTGA[A/G]GTTTAGAGAAAAAGA | 114792 |
| rs749374606 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037859 | ATAGGGAACCCAAAT[A/G]TAAGTCCACACATTT | 114792 |
| rs749383143 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953793 | CTAAATGTTATTTAT[A/G]TAATCAAACCATGAT | 114792 |
| rs749383247 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067522 | GTCTGCTTGTTTCTA[C/G]CCTCAATCTGTGGTA | 114792 |
| rs749394629 | snp | C/T | 3.29614e-05 | 0.00405951 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139231 | TCCATATTTTACATG[C/T]CCTAACCTTCAAACT | 114792 |
| rs749405825 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112593 | CTGGGACTACAGGCA[C/T]GTGCCACCACGCCCA | 114792 |
| rs749427985 | snp | C/G | 1.6476e-05 | 0.00287014 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897841 | GTTCAGGCCGCACGT[C/G]GGAACACCGGCGCAG | 114792 |
| rs749429396 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137028 | CCGGTATCAATTTTC[C/T]TCTCTGTAAATTGAA | 114792 |
| rs749436640 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026765 | TAAAATTTTAAGAGC[A/G]ATCATTAGTTTACAT | 114792 |
| rs749445656 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091621 | GATTTCTTTGCCAAG[G/T]TGGGGCACGTTGAAA | 114792 |
| rs749451219 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075012 | TTATTGTTGACGGCT[A/G]TGTTTCACTTCCTCC | 114792 |
| rs749456989 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919120 | TTTGAATCTTGGATG[C/G]AGTGGAGTTATTTGG | 114792 |
| rs749482661 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048593 | TGGTTCCCTAATAAG[A/T]TCACATGACTTTTTT | 114792 |
| rs749487334 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964660 | CCTGTCTCAACAGAA[A/G]AACAAAACAAAAACA | 114792 |
| rs749538167 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036708 | GGTGCATGGGGGTGC[C/G]AGGTCCTGGTGCAGG | 114792 |
| rs749542480 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989759 | CTTACCTGTGGTCTC[-/TT]TACATAATCCAATAT | 114792 |
| rs749601983 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959486 | CAGTTGCTGCCTTCT[C/T]CCTGTGTCCTCACGC | 114792 |
| rs749604075 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137219 | AAAGTAAATGAGTAA[C/G]AATAATCAAGAAAAT | 114792 |
| rs749604350 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993476 | GCTTCTCAAGCTTCT[A/G]TTTGGGTCTTGTTTG | 114792 |
| rs749616595 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104080 | GGTGGCTGAATCTCA[C/T]AAGTAGAGAAGATAT | 114792 |
| rs749626496 | snp | A/G | | | utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:96900099 | TGAGCTGGAGTCCAG[A/G]CCCCAGACAAGTTCT | 114792 |
| rs749649101 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047787 | AATCAAAAAGCAAAA[A/T]CCAAAAAACCCAGCC | 114792 |
| rs749660491 | snp | G/T | 1.64849e-05 | 0.00287092 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041562 | GTGTGACCAGCCTTG[G/T]CTTAAAGCAGGCTCT | 114792 |
| rs749669529 | snp | C/G | 1.64969e-05 | 0.00287196 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114279 | GCTATGACCCCCGCA[C/G]TAATTCCTGGGCAGA | 114792 |
| rs749689556 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138118 | TAACTGCAGACTTGA[A/G]AGAGCCTAATAGGTT | 114792 |
| rs749698208 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104859 | CGATTTTATGGGAAA[A/G]TTGTCTTTTTGAACT | 114792 |
| rs749701135 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131848 | ACAAGGACTTAGAAA[-/CT]CTCTGAGTTTTAGCG | 114792 |
| rs749709112 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070661 | AAAGAATATCTCTTG[A/G]AAGAGTTCACTAATA | 114792 |
| rs749712984 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041342 | TGATTTGCAGTGGTT[A/T]GTGTGAATGACACTT | 114792 |
| rs749722041 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976790 | TTTTAGTAGAGACGG[A/G]GTCTCACCAAGTTGG | 114792 |
| rs749736563 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108527 | AATAATGTTAGATGA[C/G]GTTCACAGCACAGAG | 114792 |
| rs749745763 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958200 | TAAAGAACTTATTGT[C/T]TAGGGAAGGGTTACA | 114792 |
| rs749746541 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052055 | AAATTCCTAGACAAT[A/G]TAACATACTTACACA | 114792 |
| rs749791045 | snp | A/G | 1.65274e-05 | 0.00287462 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896777 | ATCTTTGGAATCAAC[A/G]TACACATCTTTTAGA | 114792 |
| rs749804745 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116977 | TACTGTGTACTTGAG[A/G]TGAAAAACTCACTTT | 114792 |
| rs749847438 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138951 | ATAGTGTAGCATTTA[G/T]TAGGAGCTTAATAAA | 114792 |
| rs749847454 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929651 | GAGCTGAGCAATGTG[-/A]AAATGCTCAACTTTC | 114792 |
| rs749851087 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984625 | GATCCCTTTACCATT[A/T]AGTAATGGCCTTGTC | 114792 |
| rs749851559 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943671 | TCTTCTTTGGCTTTG[C/T]GGCCCCTGTAGTGCC | 114792 |
| rs749856826 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898306 | GTTAGCCGATAAAAA[C/T]GGAACTTACTGAACC | 114792 |
| rs749867662 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926464 | TAATCCTCACAACAA[-/C]CCTTTGAGGCCAATA | 114792 |
| rs749868650 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897053 | CACCTCAGCCTCCCG[A/G]CAAGCTGAGGCTACA | 114792 |
| rs749870984 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97008073 | CTCATGCAGGTGGTT[G/T]TGGTGGTGGTGACAT | 114792 |
| rs749875205 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122881 | GAAACTCTTCCCTTA[G/T]ACTAGTGTGAACCTG | 114792 |
| rs749881841 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918564 | GTAAAATAGTGATGA[A/G]CTTTCTGTGAAAATT | 114792 |
| rs749883150 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108983 | CTTCGTAGAGTAACT[A/C]AATTCATGACAGCCT | 114792 |
| rs749883597 | in-del | -/GAAGAGAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138248 | GGCTGTGCTATATAA[-/GAAGAGAG]AGGCCAGGCACAGTG | 114792 |
| rs749887767 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064142 | TTGTAGGACTTAGAA[A/G]TAAAATGGACTAATA | 114792 |
| rs749923996 | snp | C/T | | | intron-variant | NDUFAF4 | GRCh38.p7 | 6:96896065 | GAGGTCCCTCCAATA[C/T]ACTCAGCAGTGCACG | 114792 |
| rs749926288 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139171 | ATTCTATGGGCCTAC[A/G]CTCCCTTTTGCTTCC | 114792 |
| rs749949318 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033597 | ATTTTTTTTAGTACC[C/T]TCTCTACTGTTTCCC | 114792 |
| rs749961624 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980526 | CTACTTGATTGTGGT[A/G]GATTAGCTTTTTGAT | 114792 |
| rs749971086 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109380 | AAAAATATCTCAGAA[A/G]ATGCAAACTAATAGT | 114792 |
| rs750038221 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931072 | TCATGCTGAATTATG[C/T]AAATTTTATGAAAAG | 114792 |
| rs750043956 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088899 | AACATGCATTTCCTG[C/T]CTCTTCTGCCTTTAG | 114792 |
| rs750047806 | in-del | -/AG | 1.6734e-05 | 0.00289253 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896883 | ACAATATTAAAATCA[-/AG]GAAAATTTCCTGTAA | 114792 |
| rs750065107 | in-del | -/TACA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055902 | GCTTATGAAAAGTGT[-/TACA]TAAAGTTATTTTTCC | 114792 |
| rs750075088 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961653 | GCTTGGAGGTATGTA[C/T]GTGATAGAAAGTGGG | 114792 |
| rs750097172 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974978 | TCACTCTGGGAGTAA[C/T]CTATTCCTGGCAGAT | 114792 |
| rs750102704 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114112 | TCAGGAGAATGCTCT[C/T]ATAGCTGCCATTGCC | 114792 |
| rs750123056 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96923916 | AGCATGTTTTACACA[C/G]GAGTGACCTGAATGA | 114792 |
| rs750128383 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016272 | TGAAGACATTCAATG[C/T]AAGCCCATGAAAGCA | 114792 |
| rs750167462 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896596 | TCTTGCTGTCTTACA[C/G]CAGTGTGCTTAAACT | 114792 |
| rs750175166 | in-del | -/CT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911776 | AAAATTGGCCATGCC[-/CT]CTTCTTTTGAAATAT | 114792 |
| rs750190493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058577 | ATTTAATTTCCCAGG[C/T]TCTTTTACAGCTATG | 114792 |
| rs750197844 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063396 | AAAGAGAACCTATAG[A/T]GATGCAGGAACAAGA | 114792 |
| rs750209752 | snp | G/T | 1.64827e-05 | 0.00287073 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041508 | CAATGTTCAGTCTTT[G/T]TATGGTGGAAAGTGG | 114792 |
| rs750212537 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930166 | GTGAGAACATATTTG[A/T]TGCTAATGGCACAGA | 114792 |
| rs750212752 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070278 | CGAAAATGATCAAAA[A/G]GGGTGGAAATGTATC | 114792 |
| rs750240981 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065984 | AGTAAATGGTTAATG[-/A]ATTTTTTTTTACCTT | 114792 |
| rs750242567 | in-del | -/AAAAAAAAAAAAAAAAAAAAAAAAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055818 | AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAAAAAAAA]AAAACCCCTTCTTAT | 114792 |
| rs750247422 | snp | A/G | 4.96044e-05 | 0.00497993 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041593 | GGAGTTTGCATACAC[A/G]GGACAGGTATGGTAT | 114792 |
| rs750263724 | in-del | -/CTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021567 | TCTGCTTTATTCAGT[-/CTA]CTGATTAACATGTTA | 114792 |
| rs750271319 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897879 | CCGGGACACCCGGAG[A/C]ATGCGCACAAGTGAG | 114792 |
| rs750271387 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016872 | AGTTCTCACAAGAAC[C/T]GATGGTTTTATAAGA | 114792 |
| rs750277275 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134824 | TATTTTGTTAACAGT[C/T]GTGAATGTTAGTTTG | 114792 |
| rs750287876 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080421 | ATTAAACACACATGT[A/G]TTAAGCATCTGCTCC | 114792 |
| rs750292305 | snp | C/T | | | synonymous-codon, intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113809 | GTGGTTGGAACACAA[C/T]TGCCACTACCAGTAC | 114792 |
| rs750293606 | in-del | -/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029667 | CAAGATAAAGGAGGT[-/AA]ATAGTCCAATTTAAC | 114792 |
| rs750306396 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001183 | AAACTTTGGATTTGG[A/T]GAATAATGATGTGTA | 114792 |
| rs750322025 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140169 | TGAAAGAGACACACA[-/AT]GAGGAAATAGGGAGT | 114792 |
| rs750322179 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087431 | TAGAAGTGAAACTTG[A/G]TGGACAGGCTGGAGA | 114792 |
| rs750329041 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911333 | TGTGCTACTCTCAGT[C/G]CTGCAGCCTGACCCA | 114792 |
| rs750338918 | snp | A/C | 9.96777e-05 | 0.00705896 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896710 | GCCCCAAAATAAGTA[A/C]ATTGTGTATTCACTT | 114792 |
| rs750347441 | snp | A/C/T | 8.2398e-05 | 0.00641818 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130837 | AAGGAAGCTTTATGT[A/C/T]CTTGGAGGCAATGAC | 114792 |
| rs750361409 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028028 | ATTTCTCCAGCAAGG[C/G]ACAGCCTGTCATGAA | 114792 |
| rs750373954 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940753 | TTCGTACTTACTCTC[G/T]AAATGCTGTATAGTC | 114792 |
| rs750390061 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101963 | TCTTGGAGGCATATT[A/G]CCATCATATAAATTC | 114792 |
| rs750411128 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956358 | TGAAGGTCACATAAG[C/T]ACTATTGGAGCCAGA | 114792 |
| rs750442424 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937811 | CCATCCCTTCCTAGG[C/G]ACTGTTGTCACTAAT | 114792 |
| rs750477545 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106146 | TGAGTGTGTTTCACA[A/T]GAACAATAAAGGAAT | 114792 |
| rs750478777 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993886 | TGAGGTTAGGGAACC[A/G]GAGTCTTTTATAATG | 114792 |
| rs750514436 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139312 | ATGAACAGGAGGAAA[A/G]CATAGCTCTGACTGT | 114792 |
| rs750517217 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977624 | TACAGACACCAACTT[A/C]GGCCCATGAGCAATT | 114792 |
| rs750559201 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913766 | TTCCCTTAACATATG[C/T]GCACCTTAATAACTA | 114792 |
| rs750559837 | in-del | AAAAAAAAAA/C | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010127 | AGGCACTGATTTGAC[AAAAAAAAAA/C]AAAAAAAAAAAAAAA | 114792 |
| rs750570640 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141483 | AAAGGGAAAAAACCT[A/G]GATAACTTATAATTA | 114792 |
| rs750570956 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028865 | ATAAAACAATGGACT[G/T]CTTTGTATGGTGGGT | 114792 |
| rs750579032 | snp | C/G | 1.80068e-05 | 0.00300051 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975988 | TGACTTGATTGCTCT[C/G]CTTTGTAGTATTCAA | 114792 |
| rs750580887 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009321 | TTCATCTATATTTTA[A/G]ATTTAAATGTTTCTT | 114792 |
| rs750591883 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993116 | AGGCTGAGCCCTATG[C/G]AGCTTGTAATATAGA | 114792 |
| rs750592132 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973313 | ATAAAATGCAAATAC[C/T]GATTCAGTCTTAATA | 114792 |
| rs750612428 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899842 | TCCCCAAGGAAAGTA[C/T]AACTAGGATGCTGCT | 114792 |
| rs750617597 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084681 | TTTTGGAAAAAGAGC[A/G]GAGTCAGTCTGTCTT | 114792 |
| rs750623948 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117607 | AAAGATGTTAGAGTC[A/G]AATTGTACAGGCTCC | 114792 |
| rs750632523 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071315 | GTGACTCCTCTACAG[C/T]ATTTAAACACCGGGA | 114792 |
| rs750634023 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128443 | AAGAGGAAGAAGGTG[C/T]TAACATTTCTCAAAT | 114792 |
| rs750638231 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004217 | GGTTATATTCCAGGT[A/G]TTTTATTCTTTTTAT | 114792 |
| rs750658205 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915040 | CCAACCCATTAAGAA[C/G]GTCAACCCTCCTAAA | 114792 |
| rs750675767 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031328 | TAAAAATTATAAGCA[C/T]TAAGTTTTTAACATT | 114792 |
| rs750676426 | snp | C/T | 1.64825e-05 | 0.00287071 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114449 | ACTTTTGTTCAGTCC[C/T]TTGACAGATCCCTTT | 114792 |
| rs750732561 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060585 | GATTCTGGCCCCATA[C/T]TCTGCCTGGAGACCA | 114792 |
| rs750752489 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054133 | ATATATGGTCAAATT[A/G]TAATTAATATCAGGA | 114792 |
| rs750758727 | in-del | -/GC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057181 | AGTATCTTTTTTTTT[-/GC]TTTTTTTTTTTTTTT | 114792 |
| rs750758908 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970783 | GCTTATTACTATGAC[C/T]ATTGCTATTAGTTGA | 114792 |
| rs750764764 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083273 | CACGCGCCTGTGGTC[A/C]CAGCTGCTCGGGAGG | 114792 |
| rs750773060 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116809 | TATTAAATCTATCAA[C/T]CTATTACAGATCCTT | 114792 |
| rs750818649 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091772 | CTAAACAGCTTCGCA[A/C]ACCTTTGTCAATCCA | 114792 |
| rs750835053 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130590 | CTTTTGTACTTGTTC[A/T]CATGTAAGAAGCCCA | 114792 |
| rs750839377 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030386 | ATTTGCATCACTTCT[C/G]TGTGAAATAAAGAGG | 114792 |
| rs750865965 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056126 | TTTTTTTTTTTTTGA[A/G]ATGAAGTCTCGCTCT | 114792 |
| rs750871780 | snp | A/G/T | 5.16092e-05 | 0.0050796 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085094 | ATTTATTTCTAAGAG[A/G/T]TCTTTTTTCATTTTT | 114792 |
| rs750874539 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951634 | GAGCAATATGCATAC[C/G]AAAACTGGTATGTAC | 114792 |
| rs750902152 | in-del | -/GTGTGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942655 | TGCTACAGCTGTGGG[-/GTGTGT]GTGTGTGTGTGTGTG | 114792 |
| rs750911175 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110478 | CTTGCCTTTCTGGAG[C/G]CCTTTTTCAACTGGA | 114792 |
| rs750915431 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981778 | TTATTTTTAAATAAT[G/T]TTTTGACTTCTACCT | 114792 |
| rs750916569 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907048 | TAGCTAGCTGCATTT[G/T]GATAAGTGGTCTTAA | 114792 |
| rs750921858 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096742 | GCATGCCCTCTGATG[G/T]ATGAGCTCTTTTGAG | 114792 |
| rs750954509 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053087 | ATGAGGATGGATACA[C/G]ACACACACACACACA | 114792 |
| rs750961727 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097605 | GGAAGTTCTTTCACT[C/T]GGTGACCTTCACAGC | 114792 |
| rs750967479 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005950 | TGCAGAAGAGAAGAA[G/T]GTATAGTATGTACAG | 114792 |
| rs750982245 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96925232 | CTCCCCCTTTCTTCC[C/T]TCCCCCTGAGCCCAA | 114792 |
| rs750987795 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973852 | CTCAGCCTCCTGAGT[C/T]GCTGGGATTAAGGTG | 114792 |
| rs750988673 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965802 | AAAAATGACACTCAC[-/T]TTTTAGGTTTGTCCA | 114792 |
| rs750989149 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012869 | TGACATGTTTGATGT[A/G]GAAAACTTTATTATT | 114792 |
| rs751002598 | snp | A/G | | | intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97134543 | CAACAGTTCTCTATA[A/G]TGCTGGAACACTGTT | 114792 |
| rs751006274 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016809 | CTGGTGTGAGATGGT[C/T]GGATCCTGCGGTTGG | 114792 |
| rs751036334 | snp | A/C | 1.64754e-05 | 0.00287009 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114126 | TCATAGCTGCCATTG[A/C]CAACTGGAGTGAGCT | 114792 |
| rs751075127 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089724 | GGCAGAGGTTGCAGC[A/G]AGTGGAGATTGCGCC | 114792 |
| rs751084297 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995428 | TTTCTCCTCCTCTGG[C/G]TGTTCTTTTTCAAAC | 114792 |
| rs751104739 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069099 | TTCCTCAGATTGAAG[A/G]CATTGTTCTGTTTAC | 114792 |
| rs751118419 | in-del | -/TT | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140688 | TCTTAAAGGAAATTG[-/TT]TTATTTTATTCATGT | 114792 |
| rs751152642 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927289 | GTAGGATTGGTCAGC[-/A]AATGGAGCATCCTGA | 114792 |
| rs751156873 | snp | C/G | 1.6495e-05 | 0.0028718 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114243 | CCAGTGGCCGGACGT[C/G]TGCTGTGAGGACTGC | 114792 |
| rs751166674 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033901 | TTATTTTGCTATTGA[A/G]TTTTGAGTTCCTTAA | 114792 |
| rs751169167 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911226 | GAGTTGCTGACTGCA[A/T]ATTCTCTTTGTGTCT | 114792 |
| rs751183864 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056446 | CTTTGTAACACTGCT[C/T]ACTGTGGGCTTTTAT | 114792 |
| rs751186272 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058505 | TATTCATTTCCTCTT[G/T]TTTCTTTATATAGAA | 114792 |
| rs751198225 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985457 | TCCTAGATCATATCC[C/T]GCAGAGTGTTTTCCA | 114792 |
| rs751229672 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990161 | TGGAGAAAAAGACAC[A/T]CTGGCTTTTTGACTT | 114792 |
| rs751237305 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987320 | GTGTCAATTTTAGAT[C/T]TCTCCTGCTTTCTCT | 114792 |
| rs751237938 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101548 | CCAAGCCAAGTGATG[A/G]AAGTGACTTATATGC | 114792 |
| rs751241610 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087460 | GACAGATCTACAGAA[A/T]CTCATTAAATTGCTG | 114792 |
| rs751246743 | snp | A/G | 1.66991e-05 | 0.00288951 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041616 | TATGGTATTAAATGT[A/G]ATCTGTAAAGTTTAA | 114792 |
| rs751269601 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960251 | ACTGCCACTCACATG[A/G]TGACCTGTGCAGGAA | 114792 |
| rs751310409 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127046 | ACAAGAATTTTCCAT[A/G]TAACTATGTCCCTGG | 114792 |
| rs751336779 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909928 | TAGAAGATTTAAAGA[A/C]CTTTGTACTTTGCAC | 114792 |
| rs751344648 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058108 | TCCATTGATCTGTTT[-/C]TCTCTTCTTTTGCCA | 114792 |
| rs751351326 | snp | G/T | 1.65943e-05 | 0.00288043 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896724 | AAATTGTGTATTCAC[G/T]TAATTAAACACACAT | 114792 |
| rs751357448 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068238 | TTATATTGTTTTATT[A/G]ACAACCATTCTTTAT | 114792 |
| rs751358200 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047630 | TGGCCAAGTTTTTTC[A/G]TGTTTCAGACCAGTC | 114792 |
| rs751358409 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999942 | TGCATAGAGATGATT[A/G]TTGACACTTCAGGAA | 114792 |
| rs751386584 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957990 | CTTTGGAGGATTTTG[-/T]TAAGAATAATGGTAG | 114792 |
| rs751388441 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955184 | TGGATATAAGAGTTT[G/T]AACACTTGAATTTTG | 114792 |
| rs751412674 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027895 | GAGCTGTTACTGTAT[A/G]TATTTGAAAGGCTAT | 114792 |
| rs751428348 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113483 | CAGGCTGTTTCACAA[C/T]AGCATTTTCATTCTT | 114792 |
| rs751429665 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010192 | GGACACTCTATGCCA[C/T]GCTCCTGGTTCACTG | 114792 |
| rs751435598 | in-del | -/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997341 | TTTCTTGCTGTGTCA[-/TG]TGGGTGGGCCCTCCC | 114792 |
| rs751451273 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092587 | TGCATCCCAAATAAT[A/G]TTTTGCCCAGAGGAT | 114792 |
| rs751453562 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920297 | CTGAGTCTTCATTCA[A/G]CTAAGACCTATACAA | 114792 |
| rs751471079 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131237 | TGTTAAGATGGAACT[C/G]TGATACAAGTAGGAG | 114792 |
| rs751481888 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965371 | AGTGAGTTGGTCTCC[A/G]AACGATAAATGTCTG | 114792 |
| rs751485148 | snp | A/C/T | 3.38657e-05 | 0.00411484 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132603 | AAGGGTTAATTAAAA[A/C/T]ATGTAAGAAATGGAT | 114792 |
| rs751506608 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140744 | ATAAAAACGATCTTT[A/T]TGTCTTACAGAATTC | 114792 |
| rs751515270 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921391 | GTTACACTGGCGCTG[G/T]CTCCTGATGAATAGG | 114792 |
| rs751520029 | snp | G/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998914 | TTACACTTAATTTTA[G/T]AAAATCTGTTTATAG | 114792 |
| rs751558367 | in-del | -/AT | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898373 | TTTTGTGAAAGGAAA[-/AT]AATGAAAGGATGTTC | 114792 |
| rs751577682 | snp | A/G | 4.94466e-05 | 0.00497201 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132724 | TATTCAATTTGGACA[A/G]ATGAGCCTCTGGCTT | 114792 |
| rs751590176 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914512 | ATGCTTTGTCTACCT[C/G]CCTGCACTATCGCCC | 114792 |
| rs751625788 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082593 | ACTCCAGCCTTGGGC[A/G]ACAGAGCAAGATTCC | 114792 |
| rs751634304 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031162 | GGCAACTGGTGTTTC[A/G]CTGTACCAAATGGCC | 114792 |
| rs751647975 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992941 | CTCTGCTGGATTCAT[A/G]TGCATTTCCTTCAGT | 114792 |
| rs751667834 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898086 | ACGGTTGCTTTTAAC[C/G]CTGGAACTCCGAGGG | 114792 |
| rs751669564 | snp | A/G | 1.6715e-05 | 0.00289089 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976122 | CCCTGATTGCTGAGG[A/G]ACAGAAATTCCATGC | 114792 |
| rs751678068 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071120 | TCATCTCTCATTACC[A/G]CAGCTGCTCCTTGCC | 114792 |
| rs751744605 | snp | A/T | 1.65274e-05 | 0.00287462 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127358 | TATGTTGGAATATCC[A/T]ATTTTTTATTCATGA | 114792 |
| rs751754375 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002406 | ATTTAAAAATATAAC[A/G]AATATAGCTTAAGAG | 114792 |
| rs751754916 | snp | C/T | 1.65367e-05 | 0.00287543 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127506 | TCTTAATTAATGAAT[C/T]TTAAAAGATTCCAGA | 114792 |
| rs751774354 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092905 | ATTATCAGAAATTAC[A/G]GGAGACCCAACTTGT | 114792 |
| rs751781289 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013572 | CACATACACACATGT[A/G]CACGTGTCAGGTCTA | 114792 |
| rs751786420 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082020 | CAAAGCAAATAACTT[A/G]TCAGACTTATCAGTG | 114792 |
| rs751797850 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912668 | GAAAATATGCTTAGG[A/G]CTTAAACTGAAACAT | 114792 |
| rs751799776 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129637 | CTATAATCCCAGCAC[G/T]TTGGGAGGCCGAGGT | 114792 |
| rs751801380 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117060 | CATTTCTAATACCTT[-/C]AGTCATCTGCCTCTT | 114792 |
| rs751842867 | snp | A/G | 1.64833e-05 | 0.00287078 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085251 | CCTGAAGAGCCGCCC[A/G]GAAGAAGTTCTAACG | 114792 |
| rs751871359 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926107 | GTACTTGAAGGCATC[A/G]GCAATCCAGTAATTA | 114792 |
| rs751871541 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083020 | CTGTGTACTTTCCAC[A/G]TGCCAAACTTTTATG | 114792 |
| rs751873761 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070476 | TTCATATGCTATTAT[A/G]TTGGCTTTTATTCCC | 114792 |
| rs751901557 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980293 | GTATGATGTTGGTGT[G/T]GGTTTGTCATAGATG | 114792 |
| rs751907060 | in-del | -/GCA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938633 | TTCTCTCTTCCTGCA[-/GCA]GCAGCAGCAGCAGCA | 114792 |
| rs751908570 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97143071 | CTTGCCATGGAAACG[A/T]TCTAATTAAATTGAA | 114792 |
| rs751926898 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095137 | TGGAAAATTACTCAC[A/T]GCTGAAACTAAAACT | 114792 |
| rs751942997 | in-del | -/T | 1.74233e-05 | 0.0029515 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130747 | ATACACTTAAATTTC[-/T]TTTTTTCAGAATAAG | 114792 |
| rs751950595 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920077 | GGGAAAAAAACCCGA[C/T]GAGGAAGAGTGAATC | 114792 |
| rs751961161 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096707 | ATCAAGTTCTTAAGC[A/C]AAAACAACTCCTGTT | 114792 |
| rs751973762 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967941 | TCATTTGAATAGTCT[A/C]ACTGGAGGTAAATCT | 114792 |
| rs752023832 | snp | A/G | 0.0001009 | 0.00710209 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085350 | CTGGCAGGTAAGGGC[A/G]CTGTGCACGGTCGCT | 114792 |
| rs752024331 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038325 | AAACAGTTCACTAGC[-/A]AAAAAAAAAAAATCC | 114792 |
| rs752031326 | snp | C/T | 3.29468e-05 | 0.00405861 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897787 | CCTGATACCGCGAAT[C/T]ACTAGTGCTCCCATC | 114792 |
| rs752047687 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998953 | ATAACTAGAACAACG[-/TT]TTAGTTAGAAATTGA | 114792 |
| rs752053293 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948557 | GGGTCTGTTTCTTCA[C/T]GAAATAAACATGATG | 114792 |
| rs752058229 | in-del | -/AGG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908207 | ATGTACAAGGGAAAT[-/AGG]AGGAAATTTCAAGAT | 114792 |
| rs752067777 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917563 | TGTTCAATACCTCAA[A/G]TGATCATTACATTCT | 114792 |
| rs752073156 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996190 | AATCTCCATGAACGC[C/T]TACAGTTTCTGGCCA | 114792 |
| rs752087136 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964521 | AGCAGGGCGTGTTGG[C/G]CGGCGCCTGTAGTCC | 114792 |
| rs752089540 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019949 | CACTCCCGGCGAATT[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs752092838 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940811 | TGTATATAGAAATGA[A/G]GTGAGAGGCGCTCCA | 114792 |
| rs752095010 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015399 | TTGAATGGACTTTAC[A/C]AAAATGCTGATATGA | 114792 |
| rs752105983 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950181 | GAAGCACATTTTTAA[C/T]GACAGAGGCAAGTGT | 114792 |
| rs752107279 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091325 | TGCCTCCGTGTCTGT[A/G]TCATGTTGCTAATTC | 114792 |
| rs752108155 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936429 | TTTTCCTTCAAGCCT[A/G]CCTCATCCAGAGCCT | 114792 |
| rs752113864 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905682 | ATACAGTAAACATTC[A/G]AAAACTATTAGCTAT | 114792 |
| rs752117622 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928324 | TGTTGGAAATGTGGG[A/T]TAAGAGGATGATGCT | 114792 |
| rs752120764 | snp | C/G | 1.64751e-05 | 0.00287007 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897823 | ATAACATTATGCGCT[C/G]AGGTTCAGGCCGCAC | 114792 |
| rs752121578 | snp | G/T | 1.64833e-05 | 0.00287078 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114388 | AAATGAACTGCGCCA[G/T]GTTCTGCCTACAGTT | 114792 |
| rs752147390 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035278 | AACTTTGTGTTTTTG[C/T]AGTCAGAGTTTAATT | 114792 |
| rs752149033 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027789 | TCAGGCCTTCTGCCC[A/G]GCCTACAAAACTTCG | 114792 |
| rs752153024 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971132 | TGTAAGTATGTAACA[C/T]CTTATTGGTAGTCTT | 114792 |
| rs752182986 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916644 | GGCCTCTGTGCACAT[A/T]AAAATTAGAATATTA | 114792 |
| rs752204566 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972475 | ATATACTCTTTTGTA[C/T]TGATGCAGTTCTAGG | 114792 |
| rs752207345 | snp | A/G | 9.89838e-05 | 0.00703435 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064693 | CCTACAGCTGTTGGA[A/G]CTTCTCAATTTATGC | 114792 |
| rs752214577 | snp | A/C | | | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085289 | ATTGCCTGCTTCAGG[A/C]GGTGCTGAAGAGCGA | 114792 |
| rs752219479 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004465 | TATTTGGATGCCTTT[C/T]ATTTCTTTCTATTTC | 114792 |
| rs752224159 | snp | C/T | 4.77966e-05 | 0.00488835 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064585 | GCAGCATTATATTTT[C/T]AAGTGTAACTGATAG | 114792 |
| rs752256962 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101478 | AATCTTTCTCACCAA[A/G]TTTCTGACATATAAT | 114792 |
| rs752260493 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999872 | CGTCTACTACATGCA[A/C]AAAAGTTTGTGCCGG | 114792 |
| rs752294267 | in-del | -/CCGAGCGGCTGCGG | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897544 | CAACGCTCCGCCAAC[-/CCGAGCGGCTGCGG]CCGAGCAGGCTGACG | 114792 |
| rs752298045 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041416 | AACTTTTTTTTCCCC[-/T]AGTCTCTCTAGAATT | 114792 |
| rs752300176 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908525 | CATGCATCATCCTAC[A/G]CTTCTGGATATTCCC | 114792 |
| rs752324845 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990882 | GCACTTAAGGTCTTT[G/T]TTCCTTCCTTAGTCC | 114792 |
| rs752342493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068160 | ATGTCTCTTTTTTGC[C/T]GTTACCTTTCCAAAA | 114792 |
| rs752351676 | snp | A/C | 1.66524e-05 | 0.00288547 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896863 | CTAAGGAAAGGAAAA[A/C]AGTCACAATATTAAA | 114792 |
| rs752353694 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909722 | TCCAGTCCAACATTT[C/G]AGAGCTAACCAGAAA | 114792 |
| rs752357220 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067079 | TGGTTTCTCTGCCAG[A/C]GGAGTGAAGGGCAGA | 114792 |
| rs752363299 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985944 | TTGGAGGAGGAGAGG[C/T]GCTCTGATTTTTAGA | 114792 |
| rs752414900 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963784 | CACCAAAATAATATT[A/G]CCATTATTCAGTGGT | 114792 |
| rs752441413 | snp | A/C | 1.65564e-05 | 0.00287714 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897670 | GCACCACTCACGACT[A/C]ATCTGCTCTCGCAGG | 114792 |
| rs752454440 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113350 | CGTTACTCATATTGA[A/T]ACAGCACCTTGGCTT | 114792 |
| rs752481851 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138902 | CTTATAAATATACAT[G/T]TATGTATATATGTAC | 114792 |
| rs752484827 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124437 | ATAGATGCATTTGTG[A/G]AAGACAGTAAATAAT | 114792 |
| rs752507667 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944827 | AATAAAAGAAATACT[C/G]TCTTCTTTGGTGGAA | 114792 |
| rs752534664 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060512 | GACTGAGGTGGCCCA[C/T]GTCATCATGCTCTAT | 114792 |
| rs752535343 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037532 | CTGATGAAAGAAGAT[A/G]ATGCCAAAAAAAGGG | 114792 |
| rs752536009 | snp | C/T | 1.64868e-05 | 0.00287109 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132734 | GGACAAATGAGCCTC[C/T]GGCTTGTATCCAGGT | 114792 |
| rs752544135 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107609 | TGCTTTGCCAAGAAT[A/C]TCAAATAGAAGTGGC | 114792 |
| rs752554871 | snp | C/T | 1.70761e-05 | 0.00292194 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976027 | GACAGGCCAGAGGCT[C/T]TGCCACTCCGAATCT | 114792 |
| rs752565903 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070629 | TGAGGATTTTAAAGA[C/G]GAGAAAGATTCTCCT | 114792 |
| rs752592185 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998689 | GAGGCCAAGCAAGTA[C/T]TACTGAGTCCTGTGA | 114792 |
| rs752605571 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083068 | ATTATCTTTATGCCA[A/C]CCCTATGAGCTTGTT | 114792 |
| rs752608249 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046727 | GATTGTTGAACAGCT[-/G]CTTTCTCTTACTATG | 114792 |
| rs752610204 | snp | A/C | 1.76733e-05 | 0.0029726 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976002 | TCCTTTGTAGTATTC[A/C]AGAAATGCTGACAGG | 114792 |
| rs752610937 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104676 | TATAATGGTTAATGT[G/T]CAATCTCCCTTGAAA | 114792 |
| rs752620189 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964444 | GGATCACAAGGTCAG[A/G]AGATCGAGACCATCC | 114792 |
| rs752627763 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976573 | TATGTATTGTTTCGG[-/AT]ATATATATATATTTT | 114792 |
| rs752627797 | snp | A/G | 3.29516e-05 | 0.00405891 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113850 | TCCTGCAATACATCC[A/G]CTTTGGCCTAATGGA | 114792 |
| rs752634549 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933849 | AATCTCTCACTGTTA[C/T]TGCTTCTGTGGATTA | 114792 |
| rs752646323 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899473 | CGAACTTCGGGCAGT[A/G]TGAAAAAGTAATGTT | 114792 |
| rs752654080 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049558 | TGGGTAACTGAAACC[A/G]TAGAAAGCGAAACCG | 114792 |
| rs752678840 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137885 | ATAGATGAAGGCATG[A/G]GAGTGGACTAGATCA | 114792 |
| rs752698951 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091360 | TCTGTTAGATGACAT[A/T]TGCCTCATTCATTCT | 114792 |
| rs752703114 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012278 | CTGGATTATGTAGCT[C/G]GACCCAATGTAACCA | 114792 |
| rs752713592 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113970 | ACCACCAGAGCATCT[A/G]TGCACAGCCTGTCTG | 114792 |
| rs752717146 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119753 | CTGGCTTCCTGTATA[C/G]ATTTAGGGAGAGAAT | 114792 |
| rs752719510 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128308 | GCATTTCTCTCTTTG[C/T]AAAGTGTGTTTCCTG | 114792 |
| rs752720400 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113559 | CAGTGTTGCTTCACA[-/T]TTGTTTCTTACCCCT | 114792 |
| rs752775219 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966984 | ACCCTTTTCTCTTGT[A/C]TTTTTATTCAGCTGG | 114792 |
| rs752805295 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129423 | CTTTCTTTACTTATC[G/T]GTCCATTACTTAGTT | 114792 |
| rs752806387 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936277 | TCATTTCTCTAAAGT[A/G]TCTTAACTAATGAAT | 114792 |
| rs752841917 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121477 | CATAATGTCTTTCTG[C/T]GATTTTACGGTTCAG | 114792 |
| rs752862595 | snp | C/T | 3.29669e-05 | 0.00405984 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130812 | TCTACCATTCCATGG[C/T]TGCTGTACAAAGGAA | 114792 |
| rs752907710 | in-del | -/GT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942659 | ACAGCTGTGGGGTGT[-/GT]GTGTGTGTGTGTGTG | 114792 |
| rs752942307 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011589 | CTTTAGAAACTCTAT[A/G]AACTCATCTAAAACC | 114792 |
| rs752950168 | snp | A/G | 1.70877e-05 | 0.00292294 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085359 | AAGGGCGCTGTGCAC[A/G]GTCGCTTTTGGCACT | 114792 |
| rs752959939 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142968 | ACGAAGGATAGGTAA[A/C]GATATACAAGTTTTA | 114792 |
| rs752971275 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993707 | TGTTATAGATGCTGG[C/T]AGAAGACATAAGACT | 114792 |
| rs752972041 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074733 | AAGTAGGGAAATAGA[C/T]GATAATGACTTCTAT | 114792 |
| rs752975841 | in-del | -/AGAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934198 | ACAAGGCTGGTCCTC[-/AGAA]TGACCTGAGGTTGTT | 114792 |
| rs752982123 | snp | C/G | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897829 | TTATGCGCTCAGGTT[C/G]AGGCCGCACGTGGGA | 114792 |
| rs752995844 | in-del | -/CAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051006 | AAACTCCATCTCAAA[-/CAAA]CAAACAAACAAACAA | 114792 |
| rs752996720 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060933 | GGAATGGGAATCAGT[C/T]GTGGCCCTCTCCTTA | 114792 |
| rs753005221 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967797 | AAAGTACAGGATAGA[C/T]AGAGCAAGAAAATGC | 114792 |
| rs753036636 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96922885 | AAAATATAAACTTTA[A/T]ATCAATACTAAGGAG | 114792 |
| rs753036704 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096457 | ACTCCAAGCGTATAT[A/G]TTCCATTCATCACTA | 114792 |
| rs753040245 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903588 | TAAGAGGAGGCCCGA[C/T]GTGACAGCCCACAAG | 114792 |
| rs753040941 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946959 | ATTAACAGTGGGCAC[A/G]TATTTAATTCTAAAC | 114792 |
| rs753050539 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074097 | TTTGTTTGCTGCAAC[A/G]GTATATTTATGCAGG | 114792 |
| rs753059669 | in-del | -/TTAA | 3.31925e-05 | 0.00407372 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896724 | AAATTGTGTATTCAC[-/TTAA]TTAAACACACATTTA | 114792 |
| rs753066405 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100082 | AGGAGGTGGAGGTAG[C/T]AGTACGCCAAGATTG | 114792 |
| rs753069562 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995310 | TCACTCACTTTTTGA[C/T]GGGTCAGAATAACTT | 114792 |
| rs753096358 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915515 | CTTCTTTGTGATTCC[C/T]TCCTCAACTTAGAAG | 114792 |
| rs753114946 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133953 | TTAAAAAAATTAAGT[A/G]TTGTTTAGTATTATG | 114792 |
| rs753116224 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107786 | GTGATAGATAAATAA[A/G]TATGTGTGTATGTAT | 114792 |
| rs753120788 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996034 | TGGTGGGGACAAGTC[A/C]GCCTCTTCTCCCTGC | 114792 |
| rs753123333 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096942 | GAAACAGCACTGAGA[C/G]GTTAGGTCATTGGAA | 114792 |
| rs753123747 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926784 | TCCAGGCTCTAAAAC[A/G]TGACAGTTTTTTAAG | 114792 |
| rs753124826 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978917 | TGAGCACTTTTTTTA[C/T]ATGCTTGTTGGCTGC | 114792 |
| rs753143632 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042856 | AAATTTGATCCCCAG[C/T]GTTGGAGGTCGGGTC | 114792 |
| rs753180779 | in-del | -/TCATAGCTG | 1.64751e-05 | 0.00287007 | cds-indel, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114111 | ATCAGGAGAATGCTC[-/TCATAGCTG]CCATTGCCAACTGGA | 114792 |
| rs753201134 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087375 | TATTCAGCCCAGAGT[A/G]GAGATTGGGTATGCC | 114792 |
| rs753201678 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960171 | TTAAGGTTTTATCAT[A/C]TTCATCATTATCATC | 114792 |
| rs753202795 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120829 | GAAGAATTAAATCTT[C/T]GTTGCTTTAGATCCT | 114792 |
| rs753244897 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072884 | CCAAGACATAAGTTT[A/G]TGTCCCAAAGTTGTG | 114792 |
| rs753256737 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961402 | TATCTTATGTTTATT[A/G]ATTATATTAAACTAA | 114792 |
| rs753259442 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045886 | GCCATATCCCATTGC[C/T]CAGGAGTCATATGCC | 114792 |
| rs753272421 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024878 | TGTATTTGTTTCAAA[C/T]ATATATTGAAATATC | 114792 |
| rs753274259 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908400 | CGCCTAATGATTTGG[C/T]GGGATTCATTTGTGA | 114792 |
| rs753285698 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132429 | TTACTAACTTGGCTG[A/G]CTAATAAGTGTTTTG | 114792 |
| rs753312126 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106491 | CTAACACTTGTAATC[C/G]CAGCACTTTAGGAGG | 114792 |
| rs753313929 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916469 | TTACTTTCCATTAGT[C/T]TCCCTTGCATATTAC | 114792 |
| rs753341671 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049689 | GGAGTGTTGACATGG[A/G]AAGTTTGAGAAGTGT | 114792 |
| rs753347269 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097774 | AAATGTTTCCATTCC[G/T]ATTGTGCAGTGGGAA | 114792 |
| rs753353901 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132618 | TATGTAAGAAATGGA[-/T]TTTTTTTCTTTTTAT | 114792 |
| rs753360991 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003514 | TTAGTCATTTATAAA[A/T]TTTTGGTTTTGTTGC | 114792 |
| rs753366646 | snp | A/T | 8.36351e-05 | 0.00646611 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896878 | AAGTCACAATATTAA[A/T]ATCAAGGAAAATTTC | 114792 |
| rs753389931 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066667 | TGAGTATCAAAATCA[C/T]GTCGACGTAGAAACC | 114792 |
| rs753403297 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124285 | GGAATCTATTAATAT[C/T]AAATAACTGGGACTT | 114792 |
| rs753422975 | in-del | -/CAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051003 | AGCAAAACTCCATCT[-/CAAA]CAAACAAACAAACAA | 114792 |
| rs753435385 | snp | C/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048155 | AACCCAGTGGAGAGA[C/G/T]AAACTCTGCACCAAA | 114792 |
| rs753437629 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036389 | TCATTACTGGAAATT[A/G]TCATATTCCTTTAGT | 114792 |
| rs753437858 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919695 | CTTTTAATTTACTAA[C/T]GTATTTTAATATAAA | 114792 |
| rs753440982 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013939 | CTGAAAAATTAACAT[A/C]AGTGCAGTGGTCTCT | 114792 |
| rs753446533 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977359 | ACTCTTAACGAGTGT[-/G]GATAGTCTGCTTCAT | 114792 |
| rs753461681 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966069 | TAGCTCTCTCTTTTA[C/T]ACAAATCATCAGAAA | 114792 |
| rs753483158 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918704 | AGGCTACTGTGAGAC[A/T]TCTTCACATTCAGTG | 114792 |
| rs753526005 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975049 | ACTGTATAGATTCCC[A/G]TTGATATAAGCTGGA | 114792 |
| rs753530547 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907210 | CATTTAAATGTGTAG[G/T]GTTTAGTACAACAAA | 114792 |
| rs753533929 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111360 | GAGGAAGATCCTGGG[C/T]GGGCCTCCAGATTCC | 114792 |
| rs753586547 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916852 | ACGTTTATAGTGCTA[-/T]TTTTTTTGGTGCTCA | 114792 |
| rs753599425 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932166 | ATTCACTAGTCTTTC[C/T]TAGCCTGATGTCCTT | 114792 |
| rs753622925 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136342 | AAGCATACTTTATTT[C/G]CTGCTACTACTCTGA | 114792 |
| rs753626767 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018135 | AAGAGTACAGTAAGT[A/G]TAATTAATATTGAAT | 114792 |
| rs753630756 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114094 | GTACTTCAATCCTGT[C/T]GATCAGGAGAATGCT | 114792 |
| rs753633701 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060224 | TGCCAACTCACTTGA[C/T]CACAGGCAGGAGAAA | 114792 |
| rs753636780 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087104 | TTTTAAAAGCTGCTT[G/T]CTGCTGCAGGCAATA | 114792 |
| rs753639648 | snp | A/G | 0.00011533 | 0.00759287 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113994 | CTGTCTGGCAGACTC[A/G]CAGGACCAAACCACG | 114792 |
| rs753682430 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070396 | TTGCCAAATAACATT[C/G]ATATTTGGCTTTGAA | 114792 |
| rs753699514 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962997 | ACAGTAGCTGAACTT[C/T]TACACTGTTAAATGA | 114792 |
| rs753711825 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137589 | GCCCAGGCTGGAGTG[C/T]AGTGGCGCGATCTTG | 114792 |
| rs753735011 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008208 | TGGTGGGGGAAGACC[A/G]TGGCAGCCCTGTGTG | 114792 |
| rs753744571 | snp | C/T | 1.68616e-05 | 0.00290353 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976135 | GGAACAGAAATTCCA[C/T]GCTCACAAGGCAGTC | 114792 |
| rs753767363 | snp | G/T | 1.65261e-05 | 0.0028745 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896803 | TTAGAAACGACAGCA[G/T]CTTTTCATCTTTACG | 114792 |
| rs753781101 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912506 | TCCATTATCCCTTAA[A/T]ATGGCAAACTCCTAC | 114792 |
| rs753790912 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108509 | TCCACCAGCATGGCA[A/G]TGAATAATGTTAGAT | 114792 |
| rs753794391 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033108 | ATATGTCAGGCACTG[C/T]TCACTTTGTATGTAT | 114792 |
| rs753827124 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059258 | GGAGGACATTGAAGA[C/T]GGAGAACAAGGTATT | 114792 |
| rs753829025 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041486 | TTCTCCCTTTCCTCA[C/T]CTCAGGCAATGTTCA | 114792 |
| rs753847525 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140858 | GGGCAGGAAAGGGGA[C/T]TAGGGAGAAGGAAAA | 114792 |
| rs753873184 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094787 | TGGCACGGTATTACT[A/T]ATGCTTCAAGAACAG | 114792 |
| rs753874019 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965637 | ATGCCTGTTGGAGTT[A/T]GTGTTAGGCTACAAA | 114792 |
| rs753882491 | snp | A/G | 1.72594e-05 | 0.00293758 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085372 | ACGGTCGCTTTTGGC[A/G]CTGAAAAAGCATGCC | 114792 |
| rs753905376 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125397 | TCAAAGTATTTGAAC[C/T]GTCAAAGCAAAAACT | 114792 |
| rs753919564 | snp | C/T | 1.6736e-05 | 0.0028927 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130964 | GGCAAGTACCTTTGA[C/T]TAAGTAAATCAGGAA | 114792 |
| rs753934536 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011268 | TTTGAATCCTGCAAG[A/T]GGTGGTTGCTGAAAA | 114792 |
| rs753941181 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921528 | CAATTTTGGTTTTGG[A/C]ATAATTAATGCTGCT | 114792 |
| rs753941279 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936127 | GGACCTTTATAGGCA[A/G]GCTAAGTCTAATGTC | 114792 |
| rs753942330 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946654 | GTATGGGAGAAAGCA[C/T]GGTAGTGGCAGGCCA | 114792 |
| rs753965119 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079300 | ACATCACCGAGGCCA[A/G]GACTCCTCCTTCTCT | 114792 |
| rs753975138 | snp | A/C | 1.72877e-05 | 0.00293999 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113743 | TTCTCTTTCTTTCTT[A/C]CCTTTGTGTCTCCTC | 114792 |
| rs753978037 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977734 | AGTAGCAGTCACAGA[G/T]ATTTTTCAAAGATGC | 114792 |
| rs753994653 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995302 | CTGCAGGTTCACTCA[A/C]TTTTTGATGGGTCAG | 114792 |
| rs754001955 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959961 | CCTAGAATAGTTCCC[-/T]TTTTTACTGTTAGGT | 114792 |
| rs754013261 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969265 | GTAATTGCTCTGTTT[C/T]TGAAATCACGCTATC | 114792 |
| rs754016869 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000070 | GATGGCCAATGGGAC[A/G]AAGAAGGAAAAGTCA | 114792 |
| rs754083264 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995162 | GGTATATAAAGCTCC[A/G]AGCATAGTACCTGAC | 114792 |
| rs754096994 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132230 | GCTCTGCTTTATTGG[C/G]TTCTTGGGGTTGCAG | 114792 |
| rs754108901 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062573 | AGAAATATAGAGTCC[A/T]TTTTTCTTTCTTATA | 114792 |
| rs754130272 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049589 | TCGATAACGGGGGGC[A/G]GGGGGGAACTACTTT | 114792 |
| rs754145975 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044319 | TATTTGCATATGTTG[A/T]ATCATCATTGCATCC | 114792 |
| rs754151910 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092862 | AGTGCTAGAGCTGTG[C/T]GTTGCTGAGTAGCTG | 114792 |
| rs754173310 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934613 | TACTGAAACAGAGGT[A/T]ATCATTTTCTACTAA | 114792 |
| rs754191339 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929363 | CCCATCTTTCTTAAT[A/T]AGCAAGGGGCTTTTT | 114792 |
| rs754191817 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004332 | ACTGATTTTGTATTC[C/T]GAAGCTTTGCTGAGG | 114792 |
| rs754196177 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031545 | GTCTTCCTATGTTGC[C/G]CAGCCTGGTCTCAAA | 114792 |
| rs754244267 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926667 | GCCTAGACAAGACAC[A/G]TGGGAGAGAGGGTAG | 114792 |
| rs754249079 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032667 | AGCACATCAGGGGCA[A/T]TTACAACTTGGAAGA | 114792 |
| rs754253939 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945439 | GGAGAGAATAAAGGT[A/G]CACACACTTAGTTCT | 114792 |
| rs754289058 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026619 | ATAAAATGCAAGATC[G/T]AAGGGAGGGTCCACA | 114792 |
| rs754289841 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119214 | GGGTATATTCTCAGC[A/G]CATCACGCACAGTGG | 114792 |
| rs754292434 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099239 | CCACCCAGACTGCAC[A/C]CCTCAACGGTGATAT | 114792 |
| rs754305529 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007644 | TTCAGGTTGCTGTCC[A/T]TTGGATGAGGTTTTT | 114792 |
| rs754325548 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054482 | AAATGCCAGATCAAC[A/C]CACCATTGCATTTTT | 114792 |
| rs754336634 | snp | A/G | 6.59283e-05 | 0.00574106 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114409 | GCCTACAGTTGAGCG[A/G]TATTGCCCCAAGAAG | 114792 |
| rs754339189 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970973 | ATTTAAGATGCTCAC[G/T]TGATAGTTCACCAAT | 114792 |
| rs754340864 | in-del | -/AAAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938079 | GTAATGAATAATTTA[-/AAAC]AAACAAACAGAAAAA | 114792 |
| rs754376183 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080317 | GATTTGGACAAGGTT[C/T]AGAATTGGATAGGCA | 114792 |
| rs754390460 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971779 | GAACTCATAGAGTAT[A/C]CAATAGAACCATAAT | 114792 |
| rs754404997 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107406 | AAAAATACATGGTAT[-/A]AGTTAAAAACAGTTT | 114792 |
| rs754420329 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003365 | TTTTTTGCTTGTTAA[C/T]TTAAGTTCCCTATAG | 114792 |
| rs754424641 | snp | A/C/G | 3.54964e-05 | 0.00421274 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114593 | TTTAATACTGTGGCC[A/C/G]TGTGTAATTGAAAGA | 114792 |
| rs754440160 | in-del | -/CTTTA | 4.96528e-05 | 0.00498236 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132642 | TTTTTATTCAATTCT[-/CTTTA]CTTTAGGCCAAAATG | 114792 |
| rs754472091 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969553 | CCTACGTTGTCTAGT[A/G]GAGACTAGTTCCACA | 114792 |
| rs754480535 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089747 | ATTGCGCCACTACAC[C/T]CCAGCTGGGATGATA | 114792 |
| rs754492469 | snp | C/T | 1.64781e-05 | 0.00287033 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041535 | GTGGAGCTGATGAGG[C/T]TAATTTGCACGGTGT | 114792 |
| rs754492888 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016598 | CTTTCCTTGTCTTAG[A/G]TGAGACTTTGGATTT | 114792 |
| rs754506706 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066403 | TATCCCATCAGATGG[A/G]TGATCTGTTGAGATA | 114792 |
| rs754523122 | snp | C/G | 1.64955e-05 | 0.00287184 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114250 | CCGGACGTGTGCTGT[C/G]AGGACTGCCTGTCGC | 114792 |
| rs754549868 | snp | C/G | | | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041551 | TAATTTGCACGGTGT[C/G]ACCAGCCTTGGCTTA | 114792 |
| rs754559144 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937984 | TCTCAGACTCTGTAA[A/G]TAAACACACTCTCAG | 114792 |
| rs754564322 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958207 | CTTATTGTCTAGGGA[A/G]GGGTTACAGGTAGAA | 114792 |
| rs754566820 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036425 | TATGTTTCCCTGACA[C/T]TTCATGTTCCTTGTA | 114792 |
| rs754578809 | snp | C/T | 1.6947e-05 | 0.00291088 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041641 | GTTTAACATTTCAAC[C/T]ACATCTAACCAAAGG | 114792 |
| rs754587875 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912292 | TACGGAGGCTGCAGT[A/G]GTGCTTTAAAGTAAG | 114792 |
| rs754615670 | in-del | -/GTGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932486 | AAATCCCTAAGATTT[-/GTGA]GTCTTAGTGTCATTT | 114792 |
| rs754639326 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035404 | TATTATATATTTGTC[C/T]GTATATTTAATTTTG | 114792 |
| rs754641467 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065380 | AGAGACTCAAAATAT[A/T]TCCAACTTGTCTGAG | 114792 |
| rs754668919 | snp | C/T | 1.65754e-05 | 0.00287879 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896737 | ACTTAATTAAACACA[C/T]ATTTACCTGCAAGGA | 114792 |
| rs754670373 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110771 | TTGCAGGCGGGAACC[A/G]GAGCACGGGCAATGG | 114792 |
| rs754681177 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087657 | GCTATTTGATTAATA[C/T]GTGCAACCAGTAACT | 114792 |
| rs754700989 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908434 | ACATAAAAAATGTCA[C/T]ATGAATGTTATTAAC | 114792 |
| rs754705038 | in-del | -/TACTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137048 | GTAAATTGAAGACAA[-/TACTT]TACTTAACCTTATAG | 114792 |
| rs754735289 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130851 | TTCTTGGAGGCAATG[A/G]CCTAGACTACAATAA | 114792 |
| rs754749180 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076656 | GCACAATTAGGTGTA[A/C]TTATAATATTTCTAA | 114792 |
| rs754749550 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075074 | CCAAGGAACAATATA[A/T]AATTATTCATGAGCC | 114792 |
| rs754781446 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918768 | TCTTTAAAACTTGCA[C/T]TAATTTGTTTTAAAA | 114792 |
| rs754802654 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137784 | CGTGATCCACCTGCC[G/T]GACTCCCGAAGTCCT | 114792 |
| rs754830020 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081433 | GAAAGCCGTTTGCTC[C/T]CTCAAAGAATTGGCT | 114792 |
| rs754848813 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973725 | TTGAGATCTTTACAG[A/C]TTGCCTTTTTTTTTT | 114792 |
| rs754878430 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950477 | ATTATGCTCTAAGTG[A/G]TAGCTTTTATCAGTT | 114792 |
| rs754880294 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964243 | CCTTGGGTTAATCCA[C/T]GTGCGAGGCATGGGA | 114792 |
| rs754893009 | snp | C/T | 6.89619e-05 | 0.00587165 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113750 | TCTTTCTTACCTTTG[C/T]GTCTCCTCTCATCTC | 114792 |
| rs754895921 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103493 | GCTGGGATTACAGGC[A/G]CCCAGCCATGTATAA | 114792 |
| rs754919173 | in-del | -/CATCACATTATA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920628 | CTTTTACACAAACTG[-/CATCACATTATA]CCTATTGATCTTCCA | 114792 |
| rs754940134 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113847 | AGCTCCTGCAATACA[C/T]CCGCTTTGGCCTAAT | 114792 |
| rs754946370 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079370 | CACAGGATCAACACT[A/G]TCCTCAAACTGCCCT | 114792 |
| rs754975063 | in-del | -/TCTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949323 | CTCCAGCTCTGATAT[-/TCTA]GTTAGTCAGTTTTCT | 114792 |
| rs754982598 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954015 | AGTTTGCCTGTTTTT[A/G]ATAATTGTAGTTTGG | 114792 |
| rs754982875 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000156 | TTTCAGGAGGTTGAC[A/G]TATTCTGCAGAAGAC | 114792 |
| rs754993410 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117626 | TGTACAGGCTCCTGT[A/T]GCGTTTGACATTGTG | 114792 |
| rs755000026 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136461 | AATAAACAAACACTC[A/G]TGGAAAATAATGGAA | 114792 |
| rs755020263 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018142 | CAGTAAGTATAATTA[A/G]TATTGAATCGAAACT | 114792 |
| rs755023927 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910590 | TACTTAATTTGCAAA[C/T]TGTAAATGCTTGTTT | 114792 |
| rs755032526 | in-del | -/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041090 | GTTTCATTGGACTGA[-/G]GCAGAAAAAAGCAGA | 114792 |
| rs755041430 | in-del | -/CT | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898433 | CTCTCATTTAAATGC[-/CT]CTTATTTTCCTGTCC | 114792 |
| rs755109503 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955390 | TGTTCTCTATCTTCA[A/G]TAAGTTTTATGTTTT | 114792 |
| rs755125608 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020417 | TCAAAATCTTGGTAA[A/C]AAGTTTATAGAAAAA | 114792 |
| rs755127567 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009491 | TTTTAATTTGCAATA[A/G]AGCACTTGTATAAAT | 114792 |
| rs755136216 | snp | C/T | 1.67638e-05 | 0.0028951 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085121 | TTTTATTTTTTGGCA[C/T]CCAGGAATTAAATAG | 114792 |
| rs755137154 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038859 | ACTTTGGGAGGCTGA[A/G]GCAGGTGGATCACTT | 114792 |
| rs755138539 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092952 | TCTCATGAGTTAATA[A/G]TTTTTTTTCTTTCCT | 114792 |
| rs755170733 | snp | A/G | 3.31164e-05 | 0.00406904 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127514 | AATGAATTTTAAAAG[A/G]TTCCAGAGTAATTAG | 114792 |
| rs755199580 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050823 | GCCTGGCCAACATGG[C/T]AAAACCCCATCTCTA | 114792 |
| rs755220107 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956019 | CTTACAGTTCCATGT[C/T]ATGTGGCTGGTGAGG | 114792 |
| rs755221822 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125966 | AGAAGTTATGATTAC[A/C]AGTTTTCTAAAGTAA | 114792 |
| rs755221923 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141146 | TCTCTCTAGCAGTTT[C/T]ACCTAGTAAAACTAT | 114792 |
| rs755232856 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920507 | TGTGTATGGCACTGA[A/G]CAGAGCCAGCTTCAG | 114792 |
| rs755233043 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934651 | GTATAACTAATTAGG[C/G]GGATTGCTGCAGAGA | 114792 |
| rs755240885 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945521 | GTGCCTACCACTCAA[C/T]TGTCCCTTCACCCAA | 114792 |
| rs755298748 | snp | G/T | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085258 | AGCCGCCCAGAAGAA[G/T]TTCTAACGCTTCCCT | 114792 |
| rs755309323 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072077 | TACACTTCGGCTTGG[G/T]TATTTCTCAGGCACA | 114792 |
| rs755371729 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937026 | TCATCTTACCCTGTA[-/T]TTTTTTTCCCCACAG | 114792 |
| rs755386760 | snp | A/T | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897788 | CTGATACCGCGAATC[A/T]CTAGTGCTCCCATCT | 114792 |
| rs755390525 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994307 | TCATGTTTCATAAAG[C/G]CTCAATAAATATTTA | 114792 |
| rs755401964 | snp | A/G | 0.000280036 | 0.0118296 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897824 | TAACATTATGCGCTC[A/G]GGTTCAGGCCGCACG | 114792 |
| rs755403946 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015358 | ACAGGAAGATGTGGG[A/G]AAGTTTGAAGCTCCC | 114792 |
| rs755424669 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042958 | TGAGTTCTCACTGTT[A/G]ATTCCTGAAAAAGCT | 114792 |
| rs755432824 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071445 | ACTGTCCCTCAAAGC[A/G]TGGGAGCTCTGCATG | 114792 |
| rs755457374 | in-del | -/AAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905591 | TTTCTTTATCTGTAA[-/AAT]GGAAATATAACAATA | 114792 |
| rs755470387 | snp | C/T | | | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085171 | TACAGACTTGCTGAC[C/T]TCTTTAACCTCACTT | 114792 |
| rs755476989 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084750 | CCTGCCCTTACGTTA[-/T]CTTTAGTAGAGAAAA | 114792 |
| rs755501307 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114129 | TAGCTGCCATTGCCA[A/G]CTGGAGTGAGCTGGC | 114792 |
| rs755533480 | in-del | -/CTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968643 | CTATGATGTTCTCTC[-/CTT]CTCTGCTTCAACCCA | 114792 |
| rs755550910 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117822 | ATTAATCCTGAGCTC[A/T]TCATGAAGAACAGCT | 114792 |
| rs755559208 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004368 | TATCAGATGTCAGAA[C/G]TTTTGGGCAGAGGCT | 114792 |
| rs755591706 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950305 | TAAGTGTTCTAGGAA[C/T]ATAGCTCATTCTAGC | 114792 |
| rs755609084 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065194 | CAGGCAGTAAATGCC[A/G]GAGAAGGGATGAGTA | 114792 |
| rs755617591 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997357 | GTGGGTGGGCCCTCC[C/G]AAACCCCTCTCCAGA | 114792 |
| rs755617919 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046175 | GGAGCACCTTCTGAA[A/G]AAGCCAGGGGACAGC | 114792 |
| rs755636317 | snp | A/G | 1.65611e-05 | 0.00287755 | upstream-variant-2KB, stop-gained | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896746 | AACACACATTTACCT[A/G]CAAGGAAGACACAGG | 114792 |
| rs755656817 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110696 | CAGAATCCTGATTCC[A/G]TGGTTCAAAAAGGAA | 114792 |
| rs755664299 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023717 | TCTCAGATCCAGCTG[G/T]CCTAGTTCTACATGG | 114792 |
| rs755665293 | snp | G/T | 1.64988e-05 | 0.00287213 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064695 | TACAGCTGTTGGAGC[G/T]TCTCAATTTATGCTC | 114792 |
| rs755702114 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968173 | CGCCTCTGCACTCCC[C/T]ATGTGAGTCTGTTGC | 114792 |
| rs755704992 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907084 | TTACTGTAAGAAATT[A/G]TAAGTATTTATGCAA | 114792 |
| rs755706458 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917646 | TCAACTGGGCCTCCT[C/G]TGGTATTCAGGCATG | 114792 |
| rs755714364 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937777 | CTTACAGCTTCTCTG[C/T]GCCACTTTCTTTATC | 114792 |
| rs755717389 | in-del | -/CGCCCT | 1.67097e-05 | 0.00289043 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897648 | CCCCGGGCCCCGAAA[-/CGCCCT]CGCACCACTCACGAC | 114792 |
| rs755724120 | snp | C/T | 1.66674e-05 | 0.00288676 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896866 | AGGAAAGGAAAAAAG[C/T]CACAATATTAAAATC | 114792 |
| rs755763297 | snp | A/G | 5.07327e-05 | 0.00503624 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132609 | TAATTAAAATATGTA[A/G]GAAATGGATTTTTTT | 114792 |
| rs755771021 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108379 | TCAAGCTTAAGCACC[A/G]AAATATACCACAAAG | 114792 |
| rs755771952 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067145 | TACAAAGCAGCTCCA[A/G]GGGAAACCGTTGGTG | 114792 |
| rs755777391 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996322 | CCGTTAGAGGCTGGG[C/T]GTGCTCCTGCCTATG | 114792 |
| rs755792030 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122893 | TTAGACTAGTGTGAA[C/T]CTGGCCACTGCAGGT | 114792 |
| rs755816810 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940820 | AAATGAGGTGAGAGG[C/T]GCTCCATGCCCTGAA | 114792 |
| rs755841766 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017129 | GTCAGTATGACTGGA[A/G]TTTGGTGAGTAAATT | 114792 |
| rs755843727 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009711 | TCTTGCTGGACAGTA[A/G]AAGGAAAGACTGCCT | 114792 |
| rs755857494 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942329 | GATGCCCAACATGCT[G/T]CTTCACCTCAATCTC | 114792 |
| rs755861094 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962806 | TGAGTCTTGGGAAAG[C/G]TAAGAAACTACCCTA | 114792 |
| rs755864608 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035394 | AGTGTTACATTATTA[A/T]ATATTTGTCTGTATA | 114792 |
| rs755867083 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96906009 | CTCTGCCTTTTTATT[C/T]TGGTAGTCCCACCTT | 114792 |
| rs755870299 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931073 | CATGCTGAATTATGT[A/T]AATTTTATGAAAAGG | 114792 |
| rs755881503 | in-del | -/A | 5.05642e-05 | 0.00502788 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130984 | TAAATCAGGAAAAGT[-/A]GATTCAAGAAGTCAC | 114792 |
| rs755899653 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022761 | AGGCATGAGCCATGG[A/C]GCCCAGCCCTGATCA | 114792 |
| rs755960437 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96989169 | GGTTATTATGCAGAC[C/T]TGATTGTGTGGTTGC | 114792 |
| rs756010911 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069510 | ATCAGGGCTGAAGGT[A/G]TCTGAGTGCTGTTTT | 114792 |
| rs756014184 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975020 | GTCCAATACCAGTTC[C/T]GAGATTTTAGAGCAC | 114792 |
| rs756020439 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961704 | AGATGATTGGTGAGT[C/T]GGAAAGGTGAGGTAA | 114792 |
| rs756069672 | snp | C/T | 1.74066e-05 | 0.00295008 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976014 | TTCAAGAAATGCTGA[C/T]AGGCCAGAGGCTCTG | 114792 |
| rs756072702 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911367 | TACTTCCTGAGGGAC[C/G]TAGAACCAACTCAAG | 114792 |
| rs756075790 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103354 | GAGCAGCTGGGACTA[C/T]AGGCACCTGCCATCA | 114792 |
| rs756087934 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102086 | ACTTGTTTTGCTGAG[G/T]ATCAGTATGTTGATA | 114792 |
| rs756092161 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109377 | ATAAAAATATCTCAG[-/A]AAAATGCAAACTAAT | 114792 |
| rs756096560 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058609 | GTAGCCACCCAGCCA[A/G]TGAGATGTAAATGGA | 114792 |
| rs756116509 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124940 | ATATTTATTTTGACA[C/T]ACATCTTGACTATAT | 114792 |
| rs756126006 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896680 | CTACTTGCCACACTT[A/T]ATCATTTTCCTGAAG | 114792 |
| rs756127865 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972911 | CCCTTCCAGCTATGT[C/T]CTGTGGCCACGTGTG | 114792 |
| rs756144432 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016286 | GCAAGCCCATGAAAG[C/G]AGAGAGGGGGACTGT | 114792 |
| rs756149260 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920331 | TTAGTTTTCCTTTCC[A/G]TGGCATTCCACCTTC | 114792 |
| rs756162471 | snp | C/T | 5.04689e-05 | 0.00502314 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976132 | TGAGGAACAGAAATT[C/T]CATGCTCACAAGGCA | 114792 |
| rs756176059 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121592 | GAAAGAATTACATAC[C/T]ACAGGAGTCTAATGG | 114792 |
| rs756177795 | in-del | -/ATGCTAAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071869 | CCTGCCTGTAGTCTA[-/ATGCTAAT]ATGCTAATCAACACT | 114792 |
| rs756177842 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986808 | GGGAATTCCCTGACC[C/T]CTTGCACTTCCTGGG | 114792 |
| rs756192796 | snp | A/G | 3.29669e-05 | 0.00405984 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130817 | CATTCCATGGCTGCT[A/G]TACAAAGGAAGCTTT | 114792 |
| rs756237593 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078368 | GTATCGACATGGGGT[A/C]ATTTAGGTGACATTT | 114792 |
| rs756240828 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050339 | CCCCAACAGGATGTG[A/G]AAAGGTTTATTCCTC | 114792 |
| rs756243354 | snp | A/C/G | 3.29469e-05 | 0.00405864 | upstream-variant-2KB, missense, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897792 | TACCGCGAATCACTA[A/C/G]TGCTCCCATCTCCTC | 114792 |
| rs756257559 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071995 | CTATTTCTTGTCTCT[A/G]TAATGTACCCTATTC | 114792 |
| rs756259100 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096962 | GGTCATTGGAAGCCT[C/T]TTTAGTCATTTTGTG | 114792 |
| rs756264152 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031386 | TTTTGCCCAAGCTGG[A/G]GTGCAGTGGTGTGAT | 114792 |
| rs756282562 | snp | A/G | 1.70842e-05 | 0.00292264 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085360 | AGGGCGCTGTGCACG[A/G]TCGCTTTTGGCACTG | 114792 |
| rs756295640 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018321 | CAAACTAAGATTTAT[C/T]AAAAATATCAATTTG | 114792 |
| rs756298494 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993999 | GAGATACTGTATCTT[C/T]CAGGATTGTAAACAA | 114792 |
| rs756307580 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942774 | GAGATTGAAAAAGAC[C/T]TTCCCCAGGTTATTC | 114792 |
| rs756308469 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104770 | TAATTTTTAATATTC[C/T]TCCATGGTAACATTT | 114792 |
| rs756314242 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993203 | GCATAACAAAGTACC[C/T]GAAAACCTAGAGGCT | 114792 |
| rs756317482 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907409 | TCTTTTAAAACATAA[-/C]CACAAAATAACATTA | 114792 |
| rs756321094 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995057 | GCCAAATCCCGTTAC[G/T]TCTGTGAACCTATGT | 114792 |
| rs756324613 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933110 | TAGCATGGAATTAGG[A/G]CAGGATGAATTAGTT | 114792 |
| rs756329408 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934964 | GATCTTTATTTTTGC[A/G]AGAGTTCAAAATGTG | 114792 |
| rs756368008 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070622 | TCGTTTGTGAGGATT[G/T]TAAAGAGGAGAAAGA | 114792 |
| rs756400083 | snp | A/C | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897830 | TATGCGCTCAGGTTC[A/C]GGCCGCACGTGGGAA | 114792 |
| rs756401601 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060596 | CATATTCTGCCTGGA[C/G]ACCAGGAGTCCCAGT | 114792 |
| rs756416925 | in-del | -/TTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138740 | CTGCAAGGTCTTGTT[-/TTC]TTCATTTCACAGATG | 114792 |
| rs756432831 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083285 | GTCCCAGCTGCTCGG[A/G]AGGCTGAGGCAGGAG | 114792 |
| rs756433973 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912941 | AGGAACCATAACTAT[C/G]AGTTTTACTGTGGTA | 114792 |
| rs756463707 | in-del | -/AAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934448 | TTGTCATTGACACTT[-/AAC]AACAACAACAAAAAA | 114792 |
| rs756480914 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913773 | AACATATGTGCACCT[C/T]AATAACTAGGGCTCT | 114792 |
| rs756493269 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030419 | ATAACACACCATAAA[C/T]CCACACCTCCCTCTG | 114792 |
| rs756497117 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042809 | CACCCCTGCTACAGT[C/T]TGGATGTTTGTCCTC | 114792 |
| rs756522391 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116944 | AACAATCACAATTTT[A/C/T]TCAGGTTTGTTTCTC | 114792 |
| rs756533134 | snp | A/C | 1.64792e-05 | 0.00287042 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114152 | GAGCTGGCTCCCATG[A/C]CTGTGGGAAGGAGCC | 114792 |
| rs756560722 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003871 | CTTTTGTACCAATAT[C/G]ATGCTGTTTTGGTTA | 114792 |
| rs756561892 | snp | A/G | 3.30011e-05 | 0.00406195 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114276 | GTCGCTATGACCCCC[A/G]CAGTAATTCCTGGGC | 114792 |
| rs756598422 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025017 | TCAACCTCAGCTTCA[C/T]CCAAAAGAAGACCAC | 114792 |
| rs756622332 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97024771 | GTAAATGTAAGTATT[A/G]TGAAGCTAGAAAAAT | 114792 |
| rs756647321 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127620 | CTGCTTTTTGGTTCC[-/T]TTTTTTGTTTTGTTA | 114792 |
| rs756647354 | snp | C/T | 2.37408e-05 | 0.00344527 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064589 | CATTATATTTTTAAG[C/T]GTAACTGATAGTTTT | 114792 |
| rs756654005 | snp | A/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924951 | GGGCGAAGCAGAGCC[A/T]TTGTGCATCAAGGAG | 114792 |
| rs756685558 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071569 | GTTCAGCCAGCATTT[C/T]ACTTGATATGCCACA | 114792 |
| rs756687286 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947213 | ATCCAAATAAGGCAA[A/G]CACCTAACTGTAGCC | 114792 |
| rs756692842 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074868 | TTCAATTAAAAGAAA[A/C]TATATATATATATTA | 114792 |
| rs756712642 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967534 | AGGGAGAGCCCTCTC[-/TA]AGGCAATCACTTTGG | 114792 |
| rs756713563 | snp | C/T | 1.6483e-05 | 0.00287076 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114396 | TGCGCCAGGTTCTGC[C/T]TACAGTTGAGCGATA | 114792 |
| rs756715272 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97136865 | CAAAAGCTCTCTGGA[A/T]GATTATCTCATTAGT | 114792 |
| rs756716430 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129796 | ATGAGGCAGAAGAAT[C/T]GACTTGAACCTGGGA | 114792 |
| rs756719703 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073332 | TTGTTTTTTAGAAGC[C/T]ACAAATAATTAAATG | 114792 |
| rs756755591 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108558 | GTGATTTTGAAGTGG[C/T]CCATTGTTTTGAATT | 114792 |
| rs756764204 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996284 | ATGACATTTTGGAAA[A/G]TTAAATATTTGAGCA | 114792 |
| rs756777201 | in-del | -/GCTCCGTGTGCACCTTCAGCAGAGCTATCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105574 | TCTGCAAAGAGAAGG[lengthTooLong]GCAACCAGATTTTAC | 114792 |
| rs756784653 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108133 | CCTAAGCACTCTTTC[A/G]TAATGTCCTCCTAAA | 114792 |
| rs756791842 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916571 | CACCCTCTGTTAAAA[C/T]GGTACGTGAGTCCTT | 114792 |
| rs756824457 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083483 | AGCTGGATTTGAGCC[A/G]AGTCTGCCTGCCTCC | 114792 |
| rs756838558 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979071 | CAGATGCATAGTTTG[C/G]AAAATATTTTCCCCA | 114792 |
| rs756842370 | snp | A/G | 9.90557e-05 | 0.0070369 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132761 | AGGTGAGTGGTAGAA[A/G]TTCCTTTTGAAGTTT | 114792 |
| rs756845174 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917590 | TTCTTCACAGAGGAG[A/G]CAATCCTATCATTAA | 114792 |
| rs756862373 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016233 | CAGCTCCACTGACAG[C/T]TTGCACTGTGTGCCT | 114792 |
| rs756878542 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960262 | CATGATGACCTGTGC[A/G]GGAAGAGGAGGACTA | 114792 |
| rs756884883 | snp | A/G | 1.64895e-05 | 0.00287132 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139156 | AGGCAAAGAAGAAGT[A/G]TTCTATGGGCCTACA | 114792 |
| rs756899633 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942497 | TTGCCTTTTGTTGTT[C/G]TCTGGTTATCTTATG | 114792 |
| rs756914078 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113880 | ATGTGGATACTCTCC[A/T]TACAGTTGCCCTGTC | 114792 |
| rs756925278 | snp | A/C | 1.6476e-05 | 0.00287014 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114008 | CGCAGGACCAAACCA[A/C]GATTCCAGTCAGACA | 114792 |
| rs756933976 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119814 | TTCATGTAACAGCCT[C/T]ATTTTTTCATTATAA | 114792 |
| rs756934016 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134632 | TTTATCATGAAATAA[A/G]ATTGTAAATTTTAAA | 114792 |
| rs756945320 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929972 | TTTTCATGGACTCTT[A/G]ACAACATTTTCCTAC | 114792 |
| rs756954008 | in-del | -/TC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020908 | CCTTCCACCTTGCTG[-/TC]TCTATTAGCTTCCAT | 114792 |
| rs756959905 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087500 | TTACGGAACGTTCTC[A/G]CTGTAATAAAGTGCT | 114792 |
| rs756975371 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046151 | ACAGGAAGGGGGCTG[A/G]CATTTCCTGGAGCAC | 114792 |
| rs756982528 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028023 | CTAATATTTCTCCAG[C/G]AAGGGACAGCCTGTC | 114792 |
| rs757023862 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014227 | GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC | 114792 |
| rs757037434 | snp | A/G | 1.68516e-05 | 0.00290268 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976037 | AGGCTCTGCCACTCC[A/G]AATCTCACAATGACA | 114792 |
| rs757054563 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972635 | GTTTCCTTGAGAAAT[A/G]TGGTTCTTGCTTTCA | 114792 |
| rs757071354 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100119 | TGTACTCCAGCCTAG[A/G]TGACAGAGTGAGACT | 114792 |
| rs757130792 | snp | A/G | 1.69723e-05 | 0.00291305 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976142 | AAATTCCATGCTCAC[A/G]AGGCAGTCCTAGCAG | 114792 |
| rs757142250 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127088 | TAGAGATTTGTCTAT[A/G]TGTACTATGTTCACT | 114792 |
| rs757154108 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933945 | TTGAGTTTTCACTCT[G/T]TAAGGAGTGACCTTG | 114792 |
| rs757164258 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037784 | ATGTACTACAAAGCT[A/C]TAGTAACTAAATTAG | 114792 |
| rs757180579 | in-del | -/CTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062321 | CATCTATTCCCCATT[-/CTC]CTCCTCCTTAGGCCA | 114792 |
| rs757183949 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928746 | TTGGAGTGGGTAAAT[A/G]TATGGATTTTCAAAA | 114792 |
| rs757188636 | in-del | -/AATTAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011660 | TGATCATTTATCTTG[-/AATTAA]AATTAAGCATCCGAG | 114792 |
| rs757233900 | snp | A/C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059582 | AAAAATAAACTTCAG[A/C/G]TGTCAGATATAGATG | 114792 |
| rs757245899 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953679 | ATTCCCTAAAATCAC[A/G]CCATCATACATACAG | 114792 |
| rs757247058 | snp | A/G | 1.91926e-05 | 0.00309773 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130708 | TCGTTGCTGTTTTCT[A/G]ACATGGAGGTCTCCT | 114792 |
| rs757262671 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025265 | CAGCTGCTTGTTGAA[G/T]CGGTTGCTTTTCATT | 114792 |
| rs757263485 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986247 | ATTTTTGTCTCAGAG[G/T]AGTATCCGGCCGTGT | 114792 |
| rs757275912 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999951 | ATGATTGTTGACACT[G/T]CAGGAATAGAGACTA | 114792 |
| rs757279434 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103548 | ATATTACCTTGAAGC[A/G]GTCACCTTAATAAAT | 114792 |
| rs757297372 | snp | G/T | 3.45179e-05 | 0.00415424 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113746 | TCTTTCTTTCTTACC[G/T]TTGTGTCTCCTCTCA | 114792 |
| rs757312515 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992945 | GCTGGATTCATGTGC[A/G]TTTCCTTCAGTCTCA | 114792 |
| rs757340492 | snp | A/G | 1.6476e-05 | 0.00287014 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897842 | TTCAGGCCGCACGTG[A/G]GAACACCGGCGCAGG | 114792 |
| rs757352411 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078385 | TTTAGGTGACATTTC[A/G]AAGGAGAGTTGTCTA | 114792 |
| rs757356342 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068012 | AAACTTCATACAGAC[-/AC]ACACACACACACACA | 114792 |
| rs757414088 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041204 | CAGGACCAAGAGAAA[A/G]CGTTCGGTGGGCCTA | 114792 |
| rs757417448 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137908 | CTAGATCATTAAAGA[C/T]GCGTACAAAGAGGTC | 114792 |
| rs757424991 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116548 | TTTTGCACTGCATTT[C/T]CTAAGTTTTGTATGA | 114792 |
| rs757444186 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969379 | GCCCTGCTACTTTCT[A/G]CCAACCCATCCAGTC | 114792 |
| rs757450419 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002444 | AAATATTTTTCAAAC[G/T]CTATGAAGAACCCAT | 114792 |
| rs757458614 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121893 | TAGCTGATGGTGGAA[A/G]GGAGATAAAAGATCC | 114792 |
| rs757472631 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942491 | GGAGAGTTGCCTTTT[A/G]TTGTTCTCTGGTTAT | 114792 |
| rs757497047 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911460 | AATCAGCTGTCTATT[C/G]TTTGACCTTTTATTC | 114792 |
| rs757549975 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070520 | AAGGATGTCAGGAAG[C/T]GACAGCCCAGAGGCA | 114792 |
| rs757551203 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132786 | AAGTTTGTTCAAGTG[A/G]TTCAGCGAGGTTACA | 114792 |
| rs757552664 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056041 | TAATTAAATACTGTC[A/G]TATGTGACCTCACAG | 114792 |
| rs757588785 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96945655 | TGAGTGCACAACATT[G/T]GTGACTTGGGCAGCA | 114792 |
| rs757597085 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898102 | CTGGAACTCCGAGGG[A/G]GTCACCCGGGAAGCT | 114792 |
| rs757605886 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096690 | GTGGTTCCCACCATA[C/G]CATCAAGTTCTTAAG | 114792 |
| rs757608332 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012374 | AGGTTGGAGTGATGT[A/G]ATTGTTGGCTTTGAA | 114792 |
| rs757613257 | snp | A/G | 3.29989e-05 | 0.00406182 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114298 | TTCCTGGGCAGAGAT[A/G]GCACCCATGAAAAAC | 114792 |
| rs757618016 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129726 | GTCTTCACTAAAAAT[A/G]CAAAAATCAGCCAGG | 114792 |
| rs757620587 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128619 | CTCTTCTAGGCCTTT[G/T]TGGAGAGTCGATAAT | 114792 |
| rs757633720 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967974 | ATCATCCTCTGAGGG[A/G]ACAGTCAAAATATCT | 114792 |
| rs757645736 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902373 | TGAGCTTTTTTTCAT[A/G]TTTGTTGGCTGCATG | 114792 |
| rs757679999 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961520 | GCTCGTTCTGCCTGT[A/G]TGCAGCAAGCTAATC | 114792 |
| rs757680922 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114961 | AATAGGTATATATCC[A/T]AGTAATCACTATGCT | 114792 |
| rs757703054 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017346 | CTTCTTAATCTCCAG[A/G]GTTCTTACCCAATGT | 114792 |
| rs757708068 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115338 | AAGTTTGTTTGTTTT[A/T]AATTATCCGTGAATG | 114792 |
| rs757718129 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095251 | CTGCTGAGGACTGTA[A/G]TCAATTTCTCATTCT | 114792 |
| rs757729450 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936466 | TTTTGGTTGTTCAGC[A/C]CCCAAACCTTGGAAA | 114792 |
| rs757740046 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969177 | GGACCCTCAATCTGC[C/T]TATCTCCAAAGACCA | 114792 |
| rs757744330 | snp | A/C | 1.67365e-05 | 0.00289275 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896883 | ACAATATTAAAATCA[A/C]GGAAAATTTCCTGTA | 114792 |
| rs757745896 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082200 | AAAGAGACAGGACTG[C/G]CGATTGACTAGATGT | 114792 |
| rs757758999 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011707 | TTATCTCCTGCTTAT[A/G]GACATGCTGACATAA | 114792 |
| rs757785896 | snp | C/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899605 | TGTGTCAGCTGCTTT[C/G]CCTGATCCTGGCCCA | 114792 |
| rs757793057 | in-del | -/AAG | 0.000115617 | 0.00760233 | cds-indel, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139146 | TAAGCAGAGAAGGCA[-/AAG]AAGAAGTATTCTATG | 114792 |
| rs757809068 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052082 | CACAAATTACTCTAA[A/G]CACCAATAGAATTTC | 114792 |
| rs757837973 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927227 | TTTTCTTGCCATAAG[A/G]CCAAGAAGTGGAGAA | 114792 |
| rs757838041 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905750 | ACATTTTAATAATTA[A/T]AGTTTAGGTTTGATT | 114792 |
| rs757840357 | in-del | -/C | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141246 | CCCAACTAATAATAG[-/C]CTGAAAGGTAGCCTG | 114792 |
| rs757846184 | in-del | -/CAA | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997737 | CATGAACAGTCATGC[-/CAA]CAACAACAAAAAAAA | 114792 |
| rs757887926 | snp | A/G | 0.00041232 | 0.0143524 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085307 | TGCTGAAGAGCGACC[A/G]CCTGACCTCCCTGAG | 114792 |
| rs757890446 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004555 | TTCTTGTCTTGTTCC[C/T]GTTCTCAAGGGGAAT | 114792 |
| rs757894816 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111470 | CTCACTCGAACCCGC[-/T]TGCACCCAACCCCTC | 114792 |
| rs757899201 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023373 | TGAATTTATAGATAC[A/T]CTTGTAAATATAAAA | 114792 |
| rs757907003 | snp | C/T | 1.6729e-05 | 0.00289209 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139288 | CACCATCTGAAAAGC[C/T]AAGCCATCATGAACA | 114792 |
| rs757907292 | snp | A/G | 1.6476e-05 | 0.00287014 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114021 | CACGATTCCAGTCAG[A/G]CACTCTGTATATCAT | 114792 |
| rs757914299 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119736 | ACTTTCCAATTAACA[A/G]TCTGGCTTCCTGTAT | 114792 |
| rs757928800 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014465 | CTCAACAGTATGGTG[-/A]ATGGTGTTTGCACAG | 114792 |
| rs757930740 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931359 | AAAGTCACCCCCCGG[A/C]TCATGGGCTTAAGAA | 114792 |
| rs757930996 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915545 | GCAGCTCTGAGTTAG[A/G]GGAAAGAGCACTGAT | 114792 |
| rs757964265 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960202 | ATTGTCATCACCATC[A/G]TTTCCTTTTAACACG | 114792 |
| rs757982703 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026563 | GGAGATGGTCTCCAG[C/T]GGGTATTGCTTGACT | 114792 |
| rs757996893 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114115 | GGAGAATGCTCTCAT[A/G]GCTGCCATTGCCAAC | 114792 |
| rs758022671 | snp | G/T | 1.64817e-05 | 0.00287064 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041509 | AATGTTCAGTCTTTG[G/T]ATGGTGGAAAGTGGA | 114792 |
| rs758039600 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068161 | TGTCTCTTTTTTGCC[A/G]TTACCTTTCCAAAAA | 114792 |
| rs758056272 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109492 | TAGTAGACCACAAAC[A/C]AGAAATTAATCAGTA | 114792 |
| rs758065583 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078129 | GTTAAAAATCAAACC[A/G]TACTGATTTTTATGT | 114792 |
| rs758076183 | in-del | -/AGAGAGAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138250 | CTGTGCTATATAAGA[-/AGAGAGAG]GCCAGGCACAGTGGC | 114792 |
| rs758096596 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986714 | CCATTTGCTAAGACC[C/G]TTGGAAAAGCACAGT | 114792 |
| rs758116159 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054754 | ATGATAGCCATTCAT[C/T]TCTATGTATCATGTA | 114792 |
| rs758123377 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015404 | TGGACTTTACCAAAA[G/T]GCTGATATGATGTAG | 114792 |
| rs758148129 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920167 | TACTCAGTAAGGGAA[C/G]ATGGTCAGGGAAAGG | 114792 |
| rs758155528 | snp | C/T | 0.000132097 | 0.00812594 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130725 | CATGGAGGTCTCCTA[C/T]TAACAGAATACACTT | 114792 |
| rs758157064 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956866 | CTTGCAGATGTAAGA[A/G]GCACATCAGGTTTTT | 114792 |
| rs758162406 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969983 | TCCTGTTCTGGAAAT[A/C]TCAAGTTGTATAAGC | 114792 |
| rs758164965 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051540 | TGTTTCAACAGAAAG[C/T]TCCATTGCTACATAT | 114792 |
| rs758196574 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125832 | GGGATATAGAGCACT[A/G]TCTTCCTTGATGATT | 114792 |
| rs758203637 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908571 | ATCAAAAAGCAAGAC[A/G]AAAAGAGAAAAAGAC | 114792 |
| rs758207625 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025267 | GCTGCTTGTTGAATC[A/G]GTTGCTTTTCATTAG | 114792 |
| rs758244735 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125667 | GGCCATCTGTGTTTG[C/G]TGCAAATTGGTGTCT | 114792 |
| rs758250478 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973406 | TCTTCGGTTCCACTA[A/C]AAATGAAATTTTGAA | 114792 |
| rs758259251 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998712 | TCCTGTGATAAGTGG[A/T]TGTTTATGCCAAAAA | 114792 |
| rs758269839 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123086 | CATCTACTCCTGGAG[C/T]TTACTCTATTTACCA | 114792 |
| rs758284876 | snp | A/G | 4.9812e-05 | 0.00499034 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896718 | ATAAGTAAATTGTGT[A/G]TTCACTTAATTAAAC | 114792 |
| rs758314653 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063435 | TTGCAGGCAGAAGGG[A/G]TTGGGATCAAGCACA | 114792 |
| rs758317646 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019013 | AAAAATGATAGTTAA[C/G]TAGGTTGTTCTGATC | 114792 |
| rs758318130 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091364 | TTAGATGACATATGC[C/T]TCATTCATTCTTTCA | 114792 |
| rs758334829 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112312 | TAAGAATAATTCATA[C/T]CAAATATGTTGACTG | 114792 |
| rs758335760 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950132 | TGATATCTCAAAGTT[-/G]TTAAAATTATGTGCA | 114792 |
| rs758336777 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938831 | CCACATGCAGTGATG[G/T]ATGTAAGTTTCATTG | 114792 |
| rs758339411 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080960 | TTTGCTCATGCTGCT[G/T]CTTTGGCTTGGAGCA | 114792 |
| rs758341729 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048388 | AGTCACCCTAAATAC[A/G]TTTCTCTGACCCAGA | 114792 |
| rs758345908 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076712 | ACCTCATGGTGCATA[C/T]GTATGCTAAAAGTAG | 114792 |
| rs758347481 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069569 | GTTGGAAAATGTCTC[A/G]CCACCTCCAGTTACA | 114792 |
| rs758360066 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009291 | GGCTATTCAGCAGAG[-/AC]AATTTTTACCAATTT | 114792 |
| rs758367358 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008485 | TGTCTCCTAGAGGAG[C/T]GTAGGTGTCCCTGGC | 114792 |
| rs758369043 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036529 | AAGACTTTCACCTGA[A/G]ATGTGATGATACCTG | 114792 |
| rs758382581 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97141534 | TCAATAATAGAAATA[A/G]GAATTCTATTAAACT | 114792 |
| rs758395603 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964489 | AAACCCCGTCTCTAC[G/T]TAAAATACAAAAAAT | 114792 |
| rs758414985 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124439 | AGATGCATTTGTGGA[A/G]GACAGTAAATAATAA | 114792 |
| rs758420935 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009250 | GGTTTATAAACCAAA[A/G]TTCTGTTAAGAAACA | 114792 |
| rs758425581 | snp | A/G | 5.33063e-05 | 0.0051624 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96975998 | GCTCTCCTTTGTAGT[A/G]TTCAAGAAATGCTGA | 114792 |
| rs758426550 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115085 | CAGTGGTGCCATCTC[A/G]ACTCACTGCAACCTC | 114792 |
| rs758428089 | snp | A/G | 1.77209e-05 | 0.0029766 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085385 | GCACTGAAAAAGCAT[A/G]CCGTGATTGGAAGTT | 114792 |
| rs758488544 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081908 | CATGGCTAGAGCCAA[A/G]CCAGGGTGGATAGGG | 114792 |
| rs758532345 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070426 | AATGCATCATAAGAT[C/T]TGCAGTAGCCATTTT | 114792 |
| rs758534220 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051877 | CAATTGTGCTCCAGC[C/G]TTATCCTGTTTTCTG | 114792 |
| rs758552971 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991473 | TCGCAGCTGTAATGG[C/T]AGAGGGGCTATGGGT | 114792 |
| rs758554571 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128500 | ATGCTCTTTTAAAAA[A/C]TTCTGCTGGCATATT | 114792 |
| rs758566207 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912542 | CAGCTCTTCCCCTGG[C/T]GGTGAGACTTGGGGT | 114792 |
| rs758566617 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102903 | TAGGTAAACTGATGT[C/T]ATGGGGGTTTGTACA | 114792 |
| rs758568407 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100488 | TAGTCCTGTGCTTCA[C/G]TTTATGGGTTCCCCC | 114792 |
| rs758570626 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951196 | AGGGAGACTTCAACA[A/G]GCTGAGTAGGACAGG | 114792 |
| rs758583124 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011642 | ATAGATACATATTCA[A/G]AGTGATCATTTATCT | 114792 |
| rs758588537 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040248 | TATCAGTAAACAAAA[A/T]TGAATTCTCTTTATA | 114792 |
| rs758612556 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999917 | CCTAAAACATCACCA[-/C]TACAGCTTCTGCATA | 114792 |
| rs758626208 | snp | G/T | | | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114174 | GAAGGAGCCACCATT[G/T]TGTGGCAGTCATGGG | 114792 |
| rs758639485 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975917 | CGTGTTGCCTCAGTC[A/G]ATGTTCAAGGAATGA | 114792 |
| rs758653069 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027025 | AAACCAGCTGGGCGT[G/T]GTGGCGTGCACCTGT | 114792 |
| rs758670027 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927881 | CAGCGTCCACTTTTC[A/G]AGCTCTTCTGTGAGC | 114792 |
| rs758671257 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078497 | TGAGTGTTATTACCC[A/G]GAAAAATCTGTAATC | 114792 |
| rs758686059 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080742 | CCTTCCTCCCATGGA[A/G]CTTACTGGGGGATCA | 114792 |
| rs758692807 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020142 | GAGACAGGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 114792 |
| rs758707717 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062760 | CTCCTGAAACTTATA[C/T]TGAGCAGAGAAAAAT | 114792 |
| rs758715231 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069089 | GAAAGATCATTTCCT[C/T]AGATTGAAGGCATTG | 114792 |
| rs758729224 | in-del | -/CCTTCTCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071769 | TTCTCAGATATGCTA[-/CCTTCTCT]CCTTCTCTTTCTCCT | 114792 |
| rs758744516 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010840 | TTTTTCCTAAGTAGT[A/G]AAACAATCATTAGTT | 114792 |
| rs758748606 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038704 | ATATATAAATATATC[C/T]ATATATCTATATATA | 114792 |
| rs758749687 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107791 | AGATAAATAAATATG[C/T]GTGTATGTATGTGTG | 114792 |
| rs758752079 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97143047 | TCCACAGTCCTCCAT[A/G]CTTCCTTCCTTGCCA | 114792 |
| rs758755558 | snp | C/T | 1.65669e-05 | 0.00287805 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064748 | GAGCTTGCATCCTGC[C/T]CATACACCCTTCACA | 114792 |
| rs758764038 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022132 | TGCAGCCCCAGTGAA[A/C]CCACTGAAAACACAA | 114792 |
| rs758776130 | in-del | -/CA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018622 | AAAAAAAAATCAATC[-/CA]AGTATATTTATTAAT | 114792 |
| rs758778739 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005732 | ATGCCTTAATTTCAC[C/T]GTTTACCCAAGTCAT | 114792 |
| rs758784501 | in-del | -/GAAAA | 1.6623e-05 | 0.00288292 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896858 | ATAGACTAAGGAAAG[-/GAAAA]AAGTCACAATATTAA | 114792 |
| rs758820832 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978958 | TTTTTTGAAATGTGT[C/T]TGTTCATGTCTTTTG | 114792 |
| rs758824304 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127549 | TGGAATGCCAAGTGT[A/G]CACACACAGATATGC | 114792 |
| rs758844129 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967558 | CACTTTGGGGAGTAC[A/G]ATGCTTATTCTCAAA | 114792 |
| rs758847904 | snp | A/G | 1.66726e-05 | 0.00288722 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967048 | CTGAGAACCTGAGGA[A/G]CCCAGCTGGAAAATG | 114792 |
| rs758868999 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903723 | AATCCTATGTAATCA[C/T]TTCAATGGATTCCCA | 114792 |
| rs758875432 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96947000 | GTCATTGTGAAAAAA[A/G]CAGCTTGATTACTTT | 114792 |
| rs758878164 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094477 | GGCCATTCTGAGATC[A/G]TAATCAGGAGAAGCA | 114792 |
| rs758906143 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072966 | AAATACAGATATGGT[A/G]TCCTATATACAGTCT | 114792 |
| rs758925326 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994605 | TCTTTTCCTTTATAT[C/T]GGTCTGTGAGTTAAT | 114792 |
| rs758930066 | snp | A/G | 1.64836e-05 | 0.0028708 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897711 | TAGAGGGGTGTCTGG[A/G]AGCGACAGAGGGCTT | 114792 |
| rs758930153 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115218 | GCAGGGTTTCACTAC[A/T]TTGCCCAGGCTGCCC | 114792 |
| rs758943984 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026251 | GGACAAAGCATCAAA[A/T]GTGTTTGCAGAAAAA | 114792 |
| rs758947853 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056946 | GAAAACTGCCAGAGA[C/G]AAATATGTAAATGAA | 114792 |
| rs758957396 | snp | A/C | 4.94352e-05 | 0.00497143 | synonymous-codon, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139174 | CTATGGGCCTACACT[A/C]CCTTTTGCTTCCAAT | 114792 |
| rs758974530 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939619 | AAGTAATGGGAAAAA[A/C]TTCTAGGAGGAAACA | 114792 |
| rs758978952 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977799 | ATTAAATGTGATGAA[A/G]CTGAGTAATGTAGAA | 114792 |
| rs758983265 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117371 | TGGATTATAGAAGGT[A/G]GATTTTAGGGTCTTG | 114792 |
| rs759018209 | snp | C/T | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897764 | GCTCGGTTCTCTAGG[C/T]TGAAATTCCTGATAC | 114792 |
| rs759079159 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126433 | GCTCAGTATACACTA[C/T]AAGTATGAAAAGAAG | 114792 |
| rs759086152 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986649 | AATGAGCGAGGCTTC[A/G]TGGGTGTAGGACCCT | 114792 |
| rs759117772 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932026 | TTGATAGAGTCTCTC[A/G]TTCACTTGTTTCCTC | 114792 |
| rs759122573 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987623 | AGTTCATATGGAACC[A/T]AAACAGAGCCTGCAT | 114792 |
| rs759130873 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049276 | ATCACTTCTCTTGTA[C/T]CTTGGGGCCATTATT | 114792 |
| rs759169964 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137702 | ACCACGCCTGGCTAA[-/T]TTTTTGTATTTTTAG | 114792 |
| rs759176191 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009137 | TAAGATAAATGTCAG[A/T]TGCAAACCAAGGGTC | 114792 |
| rs759188704 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055354 | TCTTTTACAGTGGGA[A/G]GGGTATCCCTGAACT | 114792 |
| rs759199239 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965021 | TTCTAGTTGTCCCCA[A/G]TGTTTGTGTTTCCTA | 114792 |
| rs759208543 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990824 | TGAGCTAGACTGGCC[A/T]CTTCTCTTTAAGATG | 114792 |
| rs759215904 | in-del | -/ATA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993896 | GAACCGGAGTCTTTT[-/ATA]ATGAGTAGCAAACAT | 114792 |
| rs759230880 | snp | A/C | 1.65002e-05 | 0.00287225 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064685 | GGCAGTCACCTACAG[A/C]TGTTGGAGCTTCTCA | 114792 |
| rs759238051 | in-del | -/CCA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902198 | AACTAATTTACACTC[-/CCA]CCAATAGTGTAAAAG | 114792 |
| rs759265615 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993687 | AACTAGTCAGGCTAC[C/T]ACACTGTTATAGATG | 114792 |
| rs759277137 | snp | A/G | 1.69003e-05 | 0.00290687 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114554 | AAACACACTTTCATT[A/G]TGGTATATATTTAAA | 114792 |
| rs759278578 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140108 | TTAAAAATTACTAGA[C/T]AGAATTTGGAAACAT | 114792 |
| rs759288101 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104654 | CTTACATAAGTCTGT[A/G]GTCAGCTATAATGGT | 114792 |
| rs759312999 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070351 | TCAAGAGTATTTGCT[A/C]TCTGGCATGGGTAAT | 114792 |
| rs759316682 | snp | A/G | 1.65362e-05 | 0.00287538 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896818 | GCTTTTCATCTTTAC[A/G]AGCAATCTCTCCTTT | 114792 |
| rs759348457 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034122 | ATGTCAAGGAGCTTT[-/T]CCCCTACATTTTCTT | 114792 |
| rs759363473 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071008 | CCTTATTCCATCAGT[C/T]ACGCCCTGTGTTTCC | 114792 |
| rs759376641 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032004 | CATAATTGTATTTAA[A/G]CCTATAACAACCCTG | 114792 |
| rs759378630 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018905 | GAGATTTTTAACATT[C/T]TTCTCTCTGAAACTG | 114792 |
| rs759404617 | snp | A/G | 1.67139e-05 | 0.00289079 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897646 | GCCCCCGGGCCCCGA[A/G]ACGCCCTCGCACCAC | 114792 |
| rs759422693 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992798 | TTGCATTTTGCAGGT[A/G]TGGGAACTAAATTAC | 114792 |
| rs759439855 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900908 | AAACCAGAGAATTTG[C/T]AGGAGTCCAACTGAA | 114792 |
| rs759440354 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977471 | ATGCCTATTTAATTT[A/T]CTTTTCAATGTTTTT | 114792 |
| rs759456162 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117402 | GTTCTGTTCTCTAGA[A/G]CACAGAATGAATGTT | 114792 |
| rs759474886 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138801 | CTGCCTACTAACTAG[A/T]TTGGGCAAGTTATTT | 114792 |
| rs759514417 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965645 | TGGAGTTTGTGTTAG[A/G]CTACAAAAGATGAGT | 114792 |
| rs759542477 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913553 | TCCTGAAATTTTACC[A/G]ATAACTTTTTGCAAG | 114792 |
| rs759547607 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086566 | TCAGAGTCACAGAGC[A/G]GAGCCAGCCTTCAAA | 114792 |
| rs759572552 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028406 | CCACACAGGAGTCTC[-/T]TCTGGTCTTAGAGAA | 114792 |
| rs759577506 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071706 | ATCTTACACTCTGCC[A/G]AGACCTCATGAATTC | 114792 |
| rs759590942 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142804 | AGGTCCGTGTAATTA[C/T]TTAAGAACAAGGTAG | 114792 |
| rs759593645 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094880 | GTTGATGAGGAATGC[C/T]CACTACCTTCTCTGG | 114792 |
| rs759597321 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898990 | GTAAAGATAATCGAA[C/T]AGAATAATAATAATA | 114792 |
| rs759600635 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981209 | CAAACCATATCAGTA[C/G]GCTTCTTCTTACTGA | 114792 |
| rs759601637 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031020 | TGCACTCTACCTTTT[C/T]AAGATGTTATATGCT | 114792 |
| rs759621821 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108940 | GGCAGCAATTTACCA[C/T]AGTGGATGGAACAGT | 114792 |
| rs759646853 | in-del | -/GT | 1.64762e-05 | 0.00287016 | frameshift-variant, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114016 | CAAACCACGATTCCA[-/GT]CAGACACTCTGTATA | 114792 |
| rs759648803 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936143 | GCTAAGTCTAATGTC[A/C]CTAGAAATATAATTA | 114792 |
| rs759659740 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948222 | GGTGTGAATTTTAGT[C/G]AGACTTACCTGGATT | 114792 |
| rs759660883 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011506 | TTTGCATAATGAATG[A/G]GAAAAGTCTCTTTAA | 114792 |
| rs759677208 | snp | A/G | 4.95094e-05 | 0.00497517 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041461 | TGCTGTCAAAGTCTC[A/G]TAACTGTCTTTCTCC | 114792 |
| rs759682609 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128295 | GTATTTAATGAAGGC[A/G]TTTCTCTCTTTGCAA | 114792 |
| rs759686909 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903419 | ATTACGGTCACTCTC[A/G]TGATTACTTTACATT | 114792 |
| rs759688132 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051787 | GGTTAGTTCCTTAAA[C/T]TTCATAAGAAGATAT | 114792 |
| rs759703518 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937247 | GCCACCCCCTCTCCA[A/T]CATAGGTAACCTCTG | 114792 |
| rs759725922 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073845 | AGGAAGGAAAGGAGT[A/G]TGAAGGGGTGGAGAC | 114792 |
| rs759733995 | in-del | -/TTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019947 | ACCACTCCCGGCGAA[-/TTT]TTTTTTTTTTTTTTT | 114792 |
| rs759735699 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962118 | TTGGAAGGCTTAATC[A/C]TGTTTCACTTGCTCA | 114792 |
| rs759764092 | snp | C/T | 1.64985e-05 | 0.0028721 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041575 | TGGCTTAAAGCAGGC[C/T]CTGGAGTTTGCATAC | 114792 |
| rs759764610 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956065 | GGAAGGTGAAAGGCA[C/T]GTCTCATATGGTGGC | 114792 |
| rs759793519 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122008 | GGAGGCAGGATTTCA[A/G]CTTTCTACAGAATGA | 114792 |
| rs759805338 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905235 | CAAGAAATCATTTTC[A/G]TTTCAAAGATTATGA | 114792 |
| rs759809465 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022043 | TACCATTATGTTTTG[C/G]CTGGAGTTTTGCAGT | 114792 |
| rs759818473 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096818 | GCAAAGGAACTAATA[C/T]TGAAGTAAGCAGAGC | 114792 |
| rs759821796 | snp | C/T | 1.64933e-05 | 0.00287165 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130798 | GCTGCAGAGAAGGGT[C/T]TACCATTCCATGGCT | 114792 |
| rs759829824 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019948 | CCACTCCCGGCGAAT[-/TT]TTTTTTTTTTTTTTT | 114792 |
| rs759831623 | snp | G/T | 1.69683e-05 | 0.00291271 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085355 | AGGTAAGGGCGCTGT[G/T]CACGGTCGCTTTTGG | 114792 |
| rs759834222 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087091 | TTATAATGTAGAATT[G/T]TAAAAGCTGCTTTCT | 114792 |
| rs759839760 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045745 | GTGCACGCATGTGTG[C/T]GTGTAATTCCTGTCA | 114792 |
| rs759856991 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035173 | TTACCTCAAGGCTGG[C/T]ATAAAATGTCTTGTA | 114792 |
| rs759859719 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107108 | CCATCTTGGCTAACA[C/T]GGTGAAACCCTGTCT | 114792 |
| rs759864983 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97063314 | CTGGCTGATGGATTC[C/G]ATATAAGGCCTAAGG | 114792 |
| rs759886928 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961109 | CTATTTCAAGACATA[A/G]CAAAGAAGACATATT | 114792 |
| rs759911836 | snp | A/G | 1.65351e-05 | 0.00287528 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130938 | CACGTTGTAATTTCA[A/G]CCTGCTGACTGGCAA | 114792 |
| rs759917959 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088288 | AGGTTCCAGATGAAA[G/T]ACACCAAATTGACTA | 114792 |
| rs759970358 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910867 | GACACTCAAGGGAGT[A/G]TTTTCCAGGATAATT | 114792 |
| rs759978843 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968930 | TTCTAGACCATTACT[A/C]CACAAATTGATTGTT | 114792 |
| rs760026327 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937147 | TTGTAGCAAATGTAT[A/T]GCGTTCTGTAGCCAC | 114792 |
| rs760044976 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027356 | CTCAACGGGGCTGCA[A/G]GAAGCCATTACCAAT | 114792 |
| rs760051530 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994898 | AGCTTATGAGTCAGA[C/T]TTGAGTTTGAATCTA | 114792 |
| rs760100886 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068893 | CATGGACATTAATTT[G/T]TCATTAAGCGGCATT | 114792 |
| rs760101333 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008959 | ATTAGAAGGGCAGTA[C/T]AGTTTTAGACTGAGA | 114792 |
| rs760108881 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940311 | AATTAAATCTCAAGG[A/T]ACTGTAGCTCTTAAT | 114792 |
| rs760119596 | snp | A/G | 5.20612e-05 | 0.00510175 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114575 | TATATTTAAAAGTCA[A/G]GCTTTAATACTGTGG | 114792 |
| rs760119658 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070755 | TATGCATTTTTCTTC[-/T]TAAAAATGAAGTGTT | 114792 |
| rs760127712 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919458 | TGTGTTGATATGAAA[C/T]ATGTATTCATATGTG | 114792 |
| rs760139820 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996355 | ATTTTTAGAATTGAG[A/G]AAAGGGCATAAATCC | 114792 |
| rs760140931 | snp | A/C | 1.6703e-05 | 0.00288985 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967033 | TGCACACTTCTAAGG[A/C]TGAGAACCTGAGGAA | 114792 |
| rs760182757 | in-del | -/TAG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048846 | CCCAATTGAGCTAAA[-/TAG]TAGCACATGGAGCAA | 114792 |
| rs760184197 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138551 | AAAACAAAAACAAAA[A/G]CAACAAAAAAACCCC | 114792 |
| rs760185920 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047209 | TCTGAAAATGCATGC[-/A]ATTTCCTATCAAGTA | 114792 |
| rs760196622 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977331 | GGCAGATCTGGAATC[A/G]AAATCTATGTTTGAC | 114792 |
| rs760207424 | snp | A/C | 1.66685e-05 | 0.00288686 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064777 | CATTCCTTTCCCCAC[A/C]GTCATAAGCTGGCCC | 114792 |
| rs760222267 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968014 | AGAATAAGAGAGATG[A/G]CAAACCTGGGGAATA | 114792 |
| rs760230756 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998368 | CACATTCTGATTAAA[A/G]CAGTTCTCAAAAATT | 114792 |
| rs760238453 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104435 | AATCTTATGCTAAAG[A/G]TGAACATAATAACAT | 114792 |
| rs760238520 | in-del | -/CA | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96924804 | ACACGCACGCAGGCA[-/CA]CACACACACACACAC | 114792 |
| rs760252337 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137540 | GTTGAAGTTAAAGTC[C/T]TTTTTTTTCCCCCAG | 114792 |
| rs760276282 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125157 | TTCTGAGATAATTTT[A/T]AAAATAGTCCTCTAG | 114792 |
| rs760285364 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933431 | CTTTGTTGGATGCAG[C/G]GACAAGGCAAGGTTG | 114792 |
| rs760288857 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077722 | CAACTGTTAAGTTGT[A/G]TCTATAACCAAGCTA | 114792 |
| rs760303949 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060191 | TTGAAGATCTGAAGA[C/T]ACAAAATTTTCTGAA | 114792 |
| rs760310596 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992813 | GTGGGAACTAAATTA[C/G]GATATGTTTAAATAA | 114792 |
| rs760327414 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038601 | TGGAGAATGGTATGG[A/G]GGTTCCTCAAGAAAC | 114792 |
| rs760327660 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022335 | CTGAGAATCTTTGCA[C/G]AGCTGTTTCCTCTGC | 114792 |
| rs760360397 | snp | A/G | 1.64857e-05 | 0.00287099 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97127445 | CAGAACAGGCTAATG[A/G]TGTATGAACCTAACC | 114792 |
| rs760369602 | snp | C/G | 3.30584e-05 | 0.00406548 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897678 | CACGACTAATCTGCT[C/G]TCGCAGGAGGCTGTT | 114792 |
| rs760372651 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905139 | AACAGTTGTCCATCT[C/T]GGCCCCAGCTACAGA | 114792 |
| rs760390386 | snp | C/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008091 | GTGGTGGTGACATGA[C/G]AGGGTCAGGGCACTG | 114792 |
| rs760414686 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957536 | AATTTTAACTGGTGT[C/G]AAAGCTTTAAGAAAT | 114792 |
| rs760417342 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918615 | GATTAGAAACTAAAA[A/C]TTTGATGTATCACCA | 114792 |
| rs760419870 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007592 | CAGTTCTTGCACTGG[-/T]TCTTTCTCATGTGTA | 114792 |
| rs760425667 | snp | A/G | 1.81572e-05 | 0.00301302 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975983 | AATGTTGACTTGATT[A/G]CTCTCCTTTGTAGTA | 114792 |
| rs760436523 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983767 | CTATTTCATTCTTCT[C/T]CTTTTCTTCTTTATT | 114792 |
| rs760457567 | snp | A/G | 1.64741e-05 | 0.00286998 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897744 | TCTTGCTGATTTCCC[A/G]TTCCGCTCGGTTCTC | 114792 |
| rs760467790 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943181 | ACACACATGCCTATA[C/T]ATACACACATACATT | 114792 |
| rs760485401 | snp | A/G | 1.6517e-05 | 0.00287372 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139253 | CTTCAAACTCTTCAA[A/G]TGCCTCATCACAGGA | 114792 |
| rs760506035 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968707 | CCACTGTGCCATGTG[A/G]AAGTGTCACAACACA | 114792 |
| rs760523839 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030033 | AACTCTGTTTAATGC[C/T]TATAAAATGTAAGGG | 114792 |
| rs760533102 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052261 | CAGCAGATGCACATG[C/T]AGATGCAGACTGGTG | 114792 |
| rs760534773 | in-del | -/GTG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066532 | CAGGCTTCTTGAATA[-/GTG]GTTGAAATTTTCACT | 114792 |
| rs760553830 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070983 | CCTGAAGCTAAACCA[C/G]CTTTCTGCTCCTTAT | 114792 |
| rs760561232 | in-del | -/AAA | | | cds-indel | KLHL32 | GRCh38.p7 | 6:96900384 | GTGAATGAAAGTGAT[-/AAA]AAAATTTGAGATTAC | 114792 |
| rs760561544 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012237 | TGTAATAATGAAGTG[A/G]TGGACCTTGAGGTGG | 114792 |
| rs760570357 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956415 | TCTTCCAGAACCCAC[A/T]CTTCTTACCTGTATA | 114792 |
| rs760577141 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913296 | AATTATGGTCTATCT[A/G]GTATTGGCATTTGTC | 114792 |
| rs760577721 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912426 | TTTAGTCAATAAGTT[C/T]CCTCTTTTCCTAGCA | 114792 |
| rs760592527 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943812 | GGGAAGGGAAAAGTC[A/G]TATCTGGCAGGGGAA | 114792 |
| rs760614847 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013298 | ATAACTTTTTATTAG[A/G]ATGTCCTCTCTATTG | 114792 |
| rs760642211 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113971 | CCACCAGAGCATCTA[C/T]GCACAGCCTGTCTGG | 114792 |
| rs760652026 | in-del | -/ATG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075546 | ACATGCACAATAAAC[-/ATG]ATAACTTCTTTCCTA | 114792 |
| rs760656859 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097262 | CTCCTCCATCACCGA[A/G]CTGTCACTCCAGCCG | 114792 |
| rs760738353 | snp | A/T | 1.64741e-05 | 0.00286998 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114088 | ACTTCGGTACTTCAA[A/T]CCTGTTGATCAGGAG | 114792 |
| rs760757047 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040823 | GTTCTCACAAGATCT[A/G]ATGGTTTTATAAAGG | 114792 |
| rs760785136 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897556 | AACCCGAGCGGCTGC[A/G]GCCGAGCAGGCTGAC | 114792 |
| rs760785757 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946605 | GAGGAACAAGGGCCT[A/G]GATAATTATTTTATA | 114792 |
| rs760800476 | snp | C/G/T | 0.000115581 | 0.00760125 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064668 | AGGATGTGCTAGCAG[C/G/T]GGGCAGTCACCTACA | 114792 |
| rs760801079 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140785 | TATATCGTTATACAC[A/G]AAACATTGAAAATAC | 114792 |
| rs760807437 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958574 | GTGTTGGAAGGGGTA[C/T]TAATTTAAGAAGTTT | 114792 |
| rs760823162 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044086 | ATCTTAAAGGAGGAG[C/T]TTTCAACTTTTCACC | 114792 |
| rs760830620 | snp | A/G/T | 4.98627e-05 | 0.00499292 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896703 | TCCTGAAGCCCCAAA[A/G/T]TAAGTAAATTGTGTA | 114792 |
| rs760831311 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034275 | TATATTGAAAAGCCT[G/T]TCCTTTCCCTATTGT | 114792 |
| rs760838720 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934535 | TTAAACAACACAAAC[A/G]ATTCTCTACCAACCA | 114792 |
| rs760842410 | snp | A/G | 6.59196e-05 | 0.00574068 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132680 | CTGGAGTTGCTGTCC[A/G]TAATGGGAGAATATA | 114792 |
| rs760843608 | in-del | -/AGA | 1.64836e-05 | 0.0028708 | cds-indel, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085251 | CCTGAAGAGCCGCCC[-/AGA]AGAAGTTCTAACGCT | 114792 |
| rs760851242 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978591 | GCTATTGTGAATAGC[A/G]CTACAGTGAACATAC | 114792 |
| rs760898676 | snp | G/T | 1.67245e-05 | 0.00289171 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130962 | CTGGCAAGTACCTTT[G/T]ATTAAGTAAATCAGG | 114792 |
| rs760915785 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027249 | ATTGTGTGTTTTAGT[A/G]CTTGTCTGCTCCTGG | 114792 |
| rs760918613 | snp | C/G | 3.30486e-05 | 0.00406487 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896795 | CACATCTTTTAGAAA[C/G]GACAGCAGCTTTTCA | 114792 |
| rs760920749 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086571 | GTCACAGAGCAGAGC[C/G]AGCCTTCAAATTTAA | 114792 |
| rs760925461 | snp | C/T | 1.73219e-05 | 0.0029429 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113736 | TGTTGCTTTCTCTTT[C/T]TTTCTTACCTTTGTG | 114792 |
| rs760930870 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004239 | TCTTTTTATGGCCAT[C/T]GTGAATGTGACTGAG | 114792 |
| rs760933958 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916278 | ACTCAGATATTGTTA[G/T]AGGCACATACTCCTA | 114792 |
| rs760937583 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135420 | AAGTCATTCTCCTGC[C/T]TCAGCCTCCTGAGTA | 114792 |
| rs760947786 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032625 | GAGTCCTGCTGTATA[C/T]ACGGGATTGGTGGCA | 114792 |
| rs760964558 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113194 | CTTATTTTTTCTTTT[C/G]TTGCTTCCTGACTGT | 114792 |
| rs760964934 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940184 | AGCTGTCTTTAGGAC[A/G]TTGAGATGAAGATAT | 114792 |
| rs760968925 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084761 | GTTATCTTTAGTAGA[C/G]AAAAAGCTGTAAAAT | 114792 |
| rs761011975 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072772 | AGAGTTGCCTGATCA[A/G]TCTACTCAGTTGGAA | 114792 |
| rs761013470 | snp | A/G | 1.65108e-05 | 0.00287317 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113814 | TGGAACACAACTGCC[A/G]CTACCAGTACATGGA | 114792 |
| rs761020723 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998250 | CAGTTTCAGTCTTTC[A/T]TTCAGTCATCCACGC | 114792 |
| rs761044377 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970847 | AGTGTTCTATAGAAA[C/T]GAAATTATTTTATTA | 114792 |
| rs761090759 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015077 | CTCCCCTGCTGCCTT[A/C]TGAAGAAGGTCCTTG | 114792 |
| rs761101355 | snp | A/G | 1.92769e-05 | 0.00310453 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975950 | GAGCAGCTGGCCCAC[A/G]GGGCTGGGAAAAGGA | 114792 |
| rs761138063 | in-del | -/CTCCAATTAGCCTTGGCAACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913198 | TTAGGTACATCATAA[-/CTCCAATTAGCCTTGGCAACAC]CTCCAATTAGCCTTG | 114792 |
| rs761147571 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067831 | TTCCTCCCTGGCTTC[A/G]TCTCCAGCCACTGTG | 114792 |
| rs761177232 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037105 | TATATTATATGTTAA[A/G]TACTCCCAATAGCTT | 114792 |
| rs761205439 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96999497 | GTACTCATCTGTTTT[C/T]ACCATATTTGATGGA | 114792 |
| rs761233041 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053720 | ATATAAGTACATTTG[-/T]TTTTTTTAATTTATA | 114792 |
| rs761245565 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931893 | ATGAAAAAAAAGCCT[A/G]CTCTAAATGTGAAGA | 114792 |
| rs761260843 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081886 | GTGTGAATGTGTAGG[-/T]TGTTGTCATGGCTAG | 114792 |
| rs761272884 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946635 | AATATTGATAATTGG[A/G]CAAGTATGGGAGAAA | 114792 |
| rs761281310 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017747 | TATCTAGGTGGGGCC[A/G]TATGACTAGCCCTTG | 114792 |
| rs761284444 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962656 | TCATATTTGTATTCT[A/G]TAATAAAAGAAGACA | 114792 |
| rs761286283 | in-del | -/AA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089779 | ATGAAACTCCAGCTA[-/AA]AAAAAAAAAAAAAAA | 114792 |
| rs761288735 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974437 | TATGCTTCTGAATGT[A/G]GTTTTTAATTACTGA | 114792 |
| rs761302733 | snp | A/C | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897757 | CCGTTCCGCTCGGTT[A/C]TCTAGGTTGAAATTC | 114792 |
| rs761325110 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912580 | CTTAGCTATGCTTCA[-/G]TTTCCTCTTAAGTAA | 114792 |
| rs761342972 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931029 | ATTTCTAGAGCCCAC[A/G]TCTTTCTTGACAACT | 114792 |
| rs761353316 | in-del | -/CAAAAAAA | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010126 | CAGGCACTGATTTGA[-/CAAAAAAA]AAAAAAAAAAAAAAA | 114792 |
| rs761357405 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003643 | TTGCATTTAGCTTTA[A/G]TCCATCTTGAGTTGA | 114792 |
| rs761362132 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115678 | TCTTAGTTTTGAGAA[A/C]GGCCCTAAGTGTTCT | 114792 |
| rs761379101 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122540 | GCTAACAATGAGTGT[A/G]GCCCTCTAAATAGTG | 114792 |
| rs761390885 | snp | A/T | 1.64836e-05 | 0.0028708 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085233 | GAAACATCTCTCTGA[A/T]CTCCTGAAGAGCCGC | 114792 |
| rs761428312 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089731 | GTTGCAGCGAGTGGA[C/G]ATTGCGCCACTACAC | 114792 |
| rs761429294 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029932 | CAGTGGGCATATAGA[A/C]GATGTAAGATGTAAT | 114792 |
| rs761445625 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113373 | CTTGGCTTATGGGTT[C/G]ACATATATTACCTGA | 114792 |
| rs761449407 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137431 | CTCCACTTGTTTGTT[C/G]TTTCTTTTATTCTAG | 114792 |
| rs761468821 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016818 | GATGGTTGGATCCTG[C/T]GGTTGGTTTACCCCA | 114792 |
| rs761475604 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022628 | GCGCCTGCCACCACA[C/T]CTGGCTAATTTTTGT | 114792 |
| rs761487077 | snp | A/G | 3.30175e-05 | 0.00406296 | synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085320 | CCGCCTGACCTCCCT[A/G]AGTGAAGAGCAGATC | 114792 |
| rs761502214 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942148 | CTGCTTTACAGCCAG[A/C]GGTTACCCCACAGTC | 114792 |
| rs761520731 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96968508 | TCTGTCTGTCACCAC[C/T]TCAGCCAAGTTATTT | 114792 |
| rs761536796 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97080063 | TCTAAGTAGCCAATT[A/G]ATAGAGGAAATAATT | 114792 |
| rs761538262 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910622 | TGAGAATAAAATACA[A/T]GTTTAAAATTTTTGT | 114792 |
| rs761597212 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904623 | TTAAAATTGTAATAG[C/T]GTTTTTAATGAAGCT | 114792 |
| rs761611391 | snp | A/C | 1.6492e-05 | 0.00287154 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114228 | GGGAAGTTGAGCATG[A/C]CAGTGGCCGGACGTG | 114792 |
| rs761615451 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022000 | TCCAGACTCCAGCCA[C/T]TTCTAGTACTACCAC | 114792 |
| rs761622920 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140082 | TTGAACAGGGAGATT[-/A]TTTTTGAAGTTTAAA | 114792 |
| rs761647380 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034808 | ATGACTTTCCTGTTT[-/G]TGTACACAAATACCA | 114792 |
| rs761666044 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012124 | CTGTGTGGAACTGAG[C/T]ACTCCCTGTTCATGT | 114792 |
| rs761678357 | snp | A/G | 1.64741e-05 | 0.00286998 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114096 | ACTTCAATCCTGTTG[A/G]TCAGGAGAATGCTCT | 114792 |
| rs761678777 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979723 | TAGTTTGATAGGAAT[A/G]ACATTGAATGTGTAC | 114792 |
| rs761692678 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924041 | TAACCACAGTAATCA[C/T]ACCCTTTCTCATTTC | 114792 |
| rs761697712 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001145 | CCCATAGAATATACA[A/G]CACCAGGAGTGAACC | 114792 |
| rs761704744 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114841 | TTGTGGTTTATCTAG[A/G]TCCTTTGCTTTTTCT | 114792 |
| rs761705214 | snp | A/T | 1.65203e-05 | 0.002874 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041588 | GCTCTGGAGTTTGCA[A/T]ACACAGGACAGGTAT | 114792 |
| rs761741356 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142646 | ATTTACCTTTTAGAC[A/G]TGGGGAGACATGAGT | 114792 |
| rs761752642 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990180 | GCTTTTTGACTTGCC[A/G]GAGTTTTTGTACTAG | 114792 |
| rs761808533 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005068 | ATGGTATCAGCACTT[C/T]TTTGTACACCTGGTA | 114792 |
| rs761863661 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97043983 | TTCTCAGTTGTATTT[A/C/T]TTTTTTCTTGTCTAA | 114792 |
| rs761865407 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958743 | GGCAATGTTTCCCCA[-/T]CCCATTGGAAAGAAT | 114792 |
| rs761891184 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013576 | TACACACATGTACAC[A/G]TGTCAGGTCTAACAA | 114792 |
| rs761912501 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051605 | TTTGCCATGGTGGGT[A/C]AACAGCACAGAAATC | 114792 |
| rs761944337 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003033 | CAATAATGTGATTGC[A/G]GGTCAAATGGTAGTT | 114792 |
| rs761952170 | snp | A/C/G | 3.35904e-05 | 0.00409809 | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897635 | AGGGACTCCGCGCCC[A/C/G]CGGGCCCCGAAACGC | 114792 |
| rs761962011 | in-del | -/ACACACT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017962 | ACACTATGCTGTGTC[-/ACACACT]ATGAGTGAGTGAAGT | 114792 |
| rs761966335 | snp | G/T | 1.64814e-05 | 0.00287061 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132719 | GTGGATATTCAATTT[G/T]GACAAATGAGCCTCT | 114792 |
| rs761978785 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914978 | CTAGGACTATAGGCA[C/T]GGACCATTGCGCCCG | 114792 |
| rs761985354 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913686 | TTAACTGTTCATAGT[C/T]GGAGAAAAATTTTGA | 114792 |
| rs761987466 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113936 | ACTGCAACAGCCCTT[A/G]TCAACGAGGCCCTGG | 114792 |
| rs762016474 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071826 | GGACTATTTTTCCTG[C/G]ACTGCCCTGCAATAA | 114792 |
| rs762048957 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035821 | GCAGATCTCTTTGTA[C/T]TCAACTTATTTAGGA | 114792 |
| rs762068368 | snp | C/G | 0.00038339 | 0.0138401 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975979 | GAAAAATGTTGACTT[C/G]ATTGCTCTCCTTTGT | 114792 |
| rs762071372 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998105 | TAGCCTGCTCCTCAA[C/T]CTCCATTGAGTCTGT | 114792 |
| rs762087460 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066149 | TAAAATTACTTTTAT[G/T]TGACATTTCTACATC | 114792 |
| rs762091039 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042457 | TTGAAGAATGTGTGG[A/G]AGCTCATTTTTCTAC | 114792 |
| rs762098914 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939881 | TGATCTGGTTCAGAT[A/C]AAAGGTCATAGAAGT | 114792 |
| rs762098929 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967384 | AAAGGTATATCACAT[-/A]AAAAAAGGAATCAAA | 114792 |
| rs762098957 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130576 | TGGAATATGTGGCTC[A/T]TTTGTACTTGTTCTC | 114792 |
| rs762122975 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083081 | CAACCCTATGAGCTT[C/G]TTGAGCTCTTAAATT | 114792 |
| rs762128668 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96983837 | AGAAACCACCTCCTG[A/G]ATTCATTGATTTTTT | 114792 |
| rs762166647 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938432 | CTTCTCTTCTGGGCT[C/T]CACCTTCCGGCATGC | 114792 |
| rs762218246 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057172 | TCCTATGTGAGTATC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs762226980 | in-del | -/GGGTGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942653 | CTTGCTACAGCTGTG[-/GGGTGT]GTGTGTGTGTGTGTG | 114792 |
| rs762227527 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981618 | GGTTTGCTCTTGTTT[C/G]TCTAGTTTTTCTAGG | 114792 |
| rs762228973 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932254 | AGAAATATGGAATCA[A/T]TGTTTTTTTTTTCCA | 114792 |
| rs762241050 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952937 | ACATAAGGATTGTTT[A/G]CCACAACCCTGTGAG | 114792 |
| rs762246006 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057483 | CACCGCGCCCGGCCG[A/C]GTATCTTTTTATATG | 114792 |
| rs762310184 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990118 | CAGCCTGGTTAAGAA[C/T]ACTTGCTGGGGAACT | 114792 |
| rs762314051 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008797 | CTCTATGTCTTCCTT[A/C]CATCCACTCATTGCC | 114792 |
| rs762316543 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928220 | CTAGGTAGTAGGGGG[A/G]TTAGTGCTGGAACTT | 114792 |
| rs762316707 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955695 | TAATCCCAGCACTTT[A/G]GGAGGCTGAGGCAGG | 114792 |
| rs762317740 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047948 | AAGCAAATAGGACTG[C/T]GAACCACAATAAAGT | 114792 |
| rs762332673 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101499 | GACATATAATGGACA[C/T]TTAAGAAAACGAGAA | 114792 |
| rs762334446 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103603 | AATTTTATTTTTACA[A/G]GAGATGGTATTATTA | 114792 |
| rs762347681 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97035307 | TTCTTTTTATATTGT[G/T]TATCCATCAACAAAT | 114792 |
| rs762349969 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076102 | TAGAGCTTGAGAACC[A/G]GAGTATATTATAGTA | 114792 |
| rs762357364 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97140494 | AGACTAGTTTTTGGG[C/T]TTGCTTTGTCTATAA | 114792 |
| rs762379475 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071252 | TTCCAACAAAGGTCA[C/T]CAAAGCCTCCTTATT | 114792 |
| rs762401512 | in-del | -/TAGTAACCA | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924023 | TTATTGCTGAATTAG[-/TAGTAACCA]CAGTAATCACACCCT | 114792 |
| rs762414736 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987124 | TATTAGTCTTGCTAG[C/T]GGTCTATCAATTTTG | 114792 |
| rs762433234 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973812 | ACTGCAACCTCCACC[G/T]ACTGGGTTCAAGCAA | 114792 |
| rs762439210 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085446 | AGTGGCTTTGGTCCT[C/T]ATGGAGTTGTTTTAG | 114792 |
| rs762440224 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065028 | AGGAGCCGGGGGAGG[C/T]GTCGCTAAAAGGAGT | 114792 |
| rs762483913 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97079943 | CATTCAAAACCACTA[C/G]CGCTACCTGGATACT | 114792 |
| rs762493875 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113942 | ACAGCCCTTGTCAAC[A/G]AGGCCCTGGAATACC | 114792 |
| rs762498601 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046410 | AAAGATTAAGTTATA[-/C]CTTTGTTATACTTTG | 114792 |
| rs762528192 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070062 | ATGTTCATTTTTCTT[C/T]AACACTGAACCATTT | 114792 |
| rs762531912 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97134005 | AAGTTAGAACTTAAC[-/A]AAAAAAAACCCCTAC | 114792 |
| rs762543854 | snp | A/G | 3.29489e-05 | 0.00405874 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897818 | TCCTCATAACATTAT[A/G]CGCTCAGGTTCAGGC | 114792 |
| rs762556014 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054974 | AAAAATTGATTCCAG[A/C]TTGTGGCATCTTTGG | 114792 |
| rs762571299 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069015 | CATTTTATCATTGTA[A/C]GGGAAACAGAGAAGG | 114792 |
| rs762571370 | snp | A/C | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039669 | TACTAAAAATACAAA[A/C]ATTAGCCAGGAGTGG | 114792 |
| rs762574907 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102593 | CAATCCCAGCCATCA[A/G]TGACTAGATGGATGA | 114792 |
| rs762586580 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921950 | AGCTGAGAAAAACAA[A/G]AAAGTGTTACCTACT | 114792 |
| rs762603564 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038638 | TGTAGCTAGCATATG[A/G]CTCAGCAATTTTACT | 114792 |
| rs762607540 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985239 | TTTCTGCCAAGAGAT[A/C]AGCTGTTAGTCTGAT | 114792 |
| rs762629470 | snp | A/G | 1.64827e-05 | 0.00287073 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897853 | CGTGGGAACACCGGC[A/G]CAGGACAACTCCGGG | 114792 |
| rs762633625 | snp | C/T | 4.94874e-05 | 0.00497406 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114240 | ATGCCAGTGGCCGGA[C/T]GTGTGCTGTGAGGAC | 114792 |
| rs762672719 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092434 | CCAACTTACAAATTT[C/G]TACCACTTCTTAATT | 114792 |
| rs762682767 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978489 | TCATTCTTTTTTATG[A/C]CTGTGTAGTATTCCA | 114792 |
| rs762684107 | snp | C/T | | | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97127454 | CTAATGGTGTATGAA[C/T]CTAACCAGGTAAGAA | 114792 |
| rs762707075 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128064 | GGCAATTGCCTGCTG[A/T]ATTTTGCCATTTCTA | 114792 |
| rs762713078 | in-del | -/AATT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915703 | TTTATTAAGAGTGAG[-/AATT]AATAATGCTCTGTAA | 114792 |
| rs762721674 | snp | A/T | 1.64879e-05 | 0.00287118 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114350 | GGTGCCATGGAGGAA[A/T]ACCTCTATGCAGTTG | 114792 |
| rs762748126 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921266 | GACTAGTTGATTATG[C/T]TGAATTAGACTGAAA | 114792 |
| rs762762435 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094354 | GAAGCCTCAACATTT[A/G]TTGTTGAATACTGAC | 114792 |
| rs762793619 | snp | A/G | 4.97657e-05 | 0.00498802 | intron-variant | KLHL32 | GRCh38.p7 | 6:97041602 | ATACACAGGACAGGT[A/G]TGGTATTAAATGTGA | 114792 |
| rs762799149 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998777 | GTTAAGTTCTTTTCT[C/T]TCTCTGCCACCTGTA | 114792 |
| rs762816970 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935851 | AATCTCTATGCAATA[A/G]TATGACCTTTTTCTA | 114792 |
| rs762836549 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009821 | TAATCTTAATTCTAG[A/T]GTCTTAAAAAATGTA | 114792 |
| rs762839769 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049331 | GATACTGCCACAGTG[A/G]TCTGATAACCCAGAG | 114792 |
| rs762854054 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902885 | TCAGGTTTGTCAAAG[A/G]TCAAATGATCATAGG | 114792 |
| rs762861480 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966717 | TTTGGCCATTCCATC[G/T]CTTGTTTTAATTTTT | 114792 |
| rs762862084 | snp | A/G | 3.37764e-05 | 0.00410938 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130984 | TAAATCAGGAAAAGT[A/G]GATTCAAGAAGTCAC | 114792 |
| rs762867232 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97105993 | CTGGAAATCGGAGAA[C/T]AACATTTTCATTGTT | 114792 |
| rs762888030 | in-del | -/TTAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932203 | ATAGAACTGACTGGG[-/TTAT]TTTTTTTTTTTTTTT | 114792 |
| rs762889495 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011099 | TGGGAGGAGGGACAG[C/T]GTTTGGACATGAGGG | 114792 |
| rs762896142 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977537 | TGGTATGAATCTCCA[A/T]ATAAATGGGAATATA | 114792 |
| rs762903902 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089589 | TTTGAAACCAGCCTG[C/T]CCAACATAGTGAAAC | 114792 |
| rs762969551 | in-del | -/ACAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129887 | GACTCTGTCTCAAAT[-/ACAAA]ACAAAACAAAACAAA | 114792 |
| rs763050608 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023272 | GGCATAGGACTGGTT[A/G]GCAAAAGATCTTTCC | 114792 |
| rs763056427 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969035 | CTAACTGTAGTCGGG[C/G]TCATTGTCCTTTATT | 114792 |
| rs763057420 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979704 | CTGTGAAAAACATCA[C/T]TGGTAGTTTGATAGG | 114792 |
| rs763060500 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097433 | CGGATGTTTAATGGG[C/T]GCTTGCTGGCTACAC | 114792 |
| rs763061118 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937509 | ATGTGTGTCTGTCGG[A/G]CAACAATCCTGAGGT | 114792 |
| rs763065562 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002959 | AATGCTGCACTGAAC[A/G]TGCATGTGTCTTTAT | 114792 |
| rs763065904 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97049107 | AAGACCCCAGTGGAT[A/G]CCTGAAACCTCAGAT | 114792 |
| rs763088468 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103819 | TATCAAAACTCTCTG[C/T]GCTACAGAAACCTGT | 114792 |
| rs763104694 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926087 | TTGGGTGAACTTGTA[A/G]CACAGTACTTGAAGG | 114792 |
| rs763131225 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953123 | TACCACAAGACTGCT[A/G]TCTTGGTGAATTAGT | 114792 |
| rs763135637 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951023 | GTACTTCTCACAAAA[C/T]GTGTAATTCTGAATG | 114792 |
| rs763136845 | snp | G/T | 1.65094e-05 | 0.00287305 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041450 | TCTTGCTCCCTTGCT[G/T]TCAAAGTCTCATAAC | 114792 |
| rs763142204 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113947 | CCTTGTCAACGAGGC[C/T]CTGGAATACCACCAG | 114792 |
| rs763150661 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082903 | TAAAGAGAACACATG[C/T]TTCATTTTGACCTCT | 114792 |
| rs763163865 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957880 | TAGGGAATGAATTTC[A/G]TAATACAAACTAAAA | 114792 |
| rs763177623 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122296 | AAGTACCCATCATCT[A/G]TGTGGGTTCCTCAAG | 114792 |
| rs763182483 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977367 | ACGAGTGTGATAGTC[A/T]GCTTCATATATGGAC | 114792 |
| rs763190295 | in-del | -/CTC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044896 | ATTTATTTGAATCTT[-/CTC]GTTTTTTTTCTTAGT | 114792 |
| rs763196578 | snp | A/T | 3.33907e-05 | 0.00408586 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976119 | TCACCCTGATTGCTG[A/T]GGAACAGAAATTCCA | 114792 |
| rs763225451 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109913 | AATAGCAAATATTAC[A/G]TTTCAGAAATTTTTC | 114792 |
| rs763229336 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128600 | TCAGCCCTGGTGCTT[A/T]TTTCTCTTCTAGGCC | 114792 |
| rs763238587 | snp | A/G | 1.65111e-05 | 0.0028732 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127487 | ATGTAAGAACACCTC[A/G]TTATCTTAATTAATG | 114792 |
| rs763241024 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962387 | AATTATGTGAAAAAA[A/T]TGCTGTATTTTAAGA | 114792 |
| rs763246923 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074129 | CAGAGTCATTCCTGT[C/G]TTCACTGAAATGCAT | 114792 |
| rs763255887 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096529 | GCAGCTGTATAGATG[C/T]AGCTTTATGGTGTTT | 114792 |
| rs763274499 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052739 | GACTCGATTGAGAAG[A/G]ACTTCTTAAATATTT | 114792 |
| rs763284503 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131122 | CAGAACTGGACTCAT[A/T]TAGGTAGCTGAGCAT | 114792 |
| rs763287760 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060711 | GACATGTTGGCACAC[A/G]GTATTCAAGAGTGCC | 114792 |
| rs763311809 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061949 | ACTGGTTCTGTTTCC[A/G]TAAGTGAGAACAGCT | 114792 |
| rs763353857 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026214 | TTTTTATAAGATGTA[-/G]AGACTTTGTGTTAGC | 114792 |
| rs763401120 | in-del | -/AAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934450 | TCATTGACACTTAAC[-/AAC]AACAACAACAAAAAA | 114792 |
| rs763402046 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119052 | CCTGTCCTCACACTT[C/G]AACTTCATGGTCCAA | 114792 |
| rs763405011 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993267 | TACTGGATTTGCTTT[G/T]GCATCAGTGGTTAAT | 114792 |
| rs763414387 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123716 | TGGGGGAGGGAGATC[A/G]AAACTGCCAATCTAT | 114792 |
| rs763420657 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96994675 | AGTTGCGTGCAAAGT[A/G]CTATGAGTTCCTGTG | 114792 |
| rs763421997 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961425 | TAAACTAACTTACCT[C/T]GTCTGGTCCTTCTTT | 114792 |
| rs763424135 | in-del | -/A | 1.64849e-05 | 0.00287092 | frameshift-variant, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114378 | TTGGGGGCAGAAATG[-/A]ACTGCGCCAGGTTCT | 114792 |
| rs763447012 | in-del | -/AAAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904340 | GAGCAAGACTTTGTC[-/AAAA]AAAAAAAAAAAAAAA | 114792 |
| rs763491968 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011263 | TCTTCTTTGAATCCT[G/T]CAAGAGGTGGTTGCT | 114792 |
| rs763502629 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932659 | GCAGACTTAATCTCC[C/T]GGGCTCAAGCAATCC | 114792 |
| rs763512655 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088571 | TGGTCAAAGGGCACA[A/C]AACTTTCAGTTAGAA | 114792 |
| rs763513031 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976582 | TTTCGGATATATATA[-/T]ATATTTTTGTTTTGT | 114792 |
| rs763516972 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006838 | ACTCTTCTGCTTATA[C/G]GGTTTCTGGTGAAAG | 114792 |
| rs763519104 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019010 | ACAAAAATGATAGTT[-/A]AAGTAGGTTGTTCTG | 114792 |
| rs763538168 | in-del | -/TAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932204 | TAGAACTGACTGGGT[-/TAT]TTTTTTTTTTTTTTT | 114792 |
| rs763539022 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930948 | CCCTTGTGTTCTCTG[C/T]AGAATTAATAGTGGC | 114792 |
| rs763541520 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96974547 | CAACTGAAAATAATC[C/G]TCCCACCTTCCCACA | 114792 |
| rs763557763 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917475 | ATGCCCCAATCTGTT[A/T]TCAGAAGGAGGATGA | 114792 |
| rs763569558 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905480 | TAATGATTACTAACC[A/G]GCTTGGCATCAGACA | 114792 |
| rs763574547 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088761 | ATAAATAAGCCAAAA[C/T]ATGGCAATTCTTCAT | 114792 |
| rs763591609 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931516 | TCCTTAAATAAAATA[C/T]TTTTTCTTGTGCTAA | 114792 |
| rs763597495 | snp | C/G | 4.97987e-05 | 0.00498968 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085339 | GAAGAGCAGATCTGG[C/G]AGGTAAGGGCGCTGT | 114792 |
| rs763610197 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96954993 | GATGCTGCCAGATTC[A/C]ATGTCTGGGGAAGAC | 114792 |
| rs763620760 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038649 | TATGACTCAGCAATT[G/T]TACTACTGAGTATAT | 114792 |
| rs763628274 | snp | C/T | 1.74479e-05 | 0.00295358 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114579 | TTTAAAAGTCAAGCT[C/T]TAATACTGTGGCCAT | 114792 |
| rs763641594 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973837 | AAGCAATTCTCCTGC[C/T]TCAGCCTCCTGAGTC | 114792 |
| rs763667393 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940603 | GCCACTGCATTAAAT[C/T]CCAGAACCATACTAT | 114792 |
| rs763669165 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102614 | AGATGGATGAATATT[A/G]TCTTTTGGCTCAGAG | 114792 |
| rs763680562 | snp | A/G/T | 6.99405e-05 | 0.00591323 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085077 | TGCCTGCTCTTTCTC[A/G/T]GATTTATTTCTAAGA | 114792 |
| rs763691517 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929940 | ATTTTTAAATGAAGA[A/C]GAAATGTCTTTGGCA | 114792 |
| rs763709363 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911219 | CTCTTATGAGTTGCT[A/G]ACTGCAAATTCTCTT | 114792 |
| rs763710545 | snp | A/G | 3.29473e-05 | 0.00405864 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897749 | CTGATTTCCCGTTCC[A/G]CTCGGTTCTCTAGGT | 114792 |
| rs763710952 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916536 | ATTTTCCTTTGCCTT[G/T]TCACTTTCCCGTAAT | 114792 |
| rs763742865 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930993 | GGCGGGTACAGACCT[C/T]CTAGCCTTTCTGCAA | 114792 |
| rs763756922 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97045949 | AGAAAGCCAAATGAG[A/G]TGAAAATATATCTGG | 114792 |
| rs763761553 | snp | G/T | 1.65002e-05 | 0.00287225 | stop-gained, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139151 | AGAGAAGGCAAAGAA[G/T]AAGTATTCTATGGGC | 114792 |
| rs763771245 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97000943 | CTAAAAAGACTATCT[A/G]TTCTATGAATCCAAC | 114792 |
| rs763772420 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097276 | AGCTGTCACTCCAGC[C/T]GTCTGTTGATTGAAA | 114792 |
| rs763782916 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97016166 | TCCCCACTGGGGCAC[C/T]GCCTAGTGGAGCTGT | 114792 |
| rs763783978 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133592 | CATAAAGTACATATA[-/T]TTTTGAAGAAAATTC | 114792 |
| rs763804296 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935272 | TCCCTGATGTTGAGT[G/T]AGGTACAAACCTGCT | 114792 |
| rs763811480 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033097 | AAGAGCTTGCCATAT[G/T]TCAGGCACTGTTCAC | 114792 |
| rs763813019 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97038641 | AGCTAGCATATGACT[C/T]AGCAATTTTACTACT | 114792 |
| rs763858493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094363 | ACATTTATTGTTGAA[C/T]ACTGACTTCCTTAGA | 114792 |
| rs763863064 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990132 | ACACTTGCTGGGGAA[C/G]TAGTGCAGTTGTTTG | 114792 |
| rs763863481 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040160 | TGAGGTTTTTTTGGT[-/TTTG]TTTTTTATGACTATA | 114792 |
| rs763871280 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094060 | ATGCAGCATAAATTG[A/G]CAGTTGGGTGATGGT | 114792 |
| rs763879644 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921387 | TTGAGTTACACTGGC[A/G]CTGGCTCCTGATGAA | 114792 |
| rs763909891 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100799 | CTTGGCTCATTATTC[-/T]TTTTTTTTTTTTTTT | 114792 |
| rs763914640 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111140 | TGCCTTCAGTTGCCC[C/T]AGGACTTTATTCTGG | 114792 |
| rs763931854 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96985744 | TTTAAGGACTTCTCT[-/A]AGAATTGGTTATTCT | 114792 |
| rs763943429 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084957 | TCTAGAATAGCTGTT[C/G]TCTATGCAGAACTTT | 114792 |
| rs763994911 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108064 | TGTACATGGAAATGA[C/T]GGTCTGCTGTGTTGC | 114792 |
| rs763998984 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051273 | GAGCTGGATTTGTTG[C/T]TCTTTCCTCCATTCT | 114792 |
| rs764011627 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926094 | AACTTGTAACACAGT[A/T]CTTGAAGGCATCAGC | 114792 |
| rs764023517 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042917 | ATTCTTCGTGAAAAG[A/G]CTGATGCTCTCCCTC | 114792 |
| rs764041034 | snp | C/T | 1.68542e-05 | 0.0029029 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139302 | CCAAGCCATCATGAA[C/T]AGGAGGAAAACATAG | 114792 |
| rs764091317 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030302 | AAAATGTAGCTGTAA[A/C]TAATCTTGTGTCTGC | 114792 |
| rs764110689 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934491 | AAATCAGTTCTGATG[A/T]CAGTGCTCTCCAGAT | 114792 |
| rs764112744 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025039 | GAAGACCACATGTTT[A/T]AAGGATAATAAAGCT | 114792 |
| rs764126396 | snp | A/G | 1.67335e-05 | 0.00289248 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130963 | TGGCAAGTACCTTTG[A/G]TTAAGTAAATCAGGA | 114792 |
| rs764130124 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97125709 | GGTCCTTGGGAGACT[G/T]AGGTTGCAGTGAGCC | 114792 |
| rs764134999 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911285 | TCTCTTGCGAAGAAA[A/G]AGACTTCTGTGCACA | 114792 |
| rs764155419 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116378 | CTAGGCAGCAAATAA[G/T]TCTTTGCTAACAGAA | 114792 |
| rs764166126 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009923 | AAAGCTTTGATACCA[A/G]CTCTGGGGACTGAGG | 114792 |
| rs764191289 | snp | A/C | 1.64819e-05 | 0.00287066 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130822 | CATGGCTGCTGTACA[A/C]AGGAAGCTTTATGTT | 114792 |
| rs764219906 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130401 | ATATAGTATACCTAG[C/G]CATGTGCTTTCACTC | 114792 |
| rs764244961 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96938382 | GGTCCCTGGCCAGGT[A/G]GTACTGGGGCAGGGC | 114792 |
| rs764255166 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097465 | GAGGTAAATGAGAAC[A/G]TGCAGTCTTGGATAT | 114792 |
| rs764258043 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095451 | GTAGTGCTTTAGAAT[-/G]ATTAATTCCACACCC | 114792 |
| rs764261178 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013541 | GCTCTCCCCACCACA[C/T]ACATACACAGACACA | 114792 |
| rs764269001 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044928 | TCTGGCTAAAGTTTT[A/G]TTGATTTTATCTTTT | 114792 |
| rs764294585 | snp | G/T | 1.72928e-05 | 0.00294043 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113741 | CTTTCTCTTTCTTTC[G/T]TACCTTTGTGTCTCC | 114792 |
| rs764312363 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905551 | ATAATTTTGTGGTAA[C/G]CTCCTTAAATTTTCT | 114792 |
| rs764329915 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913561 | TTTTACCAATAACTT[C/T]TTGCAAGCGGTGCAA | 114792 |
| rs764330138 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937601 | TTTCTATTAATGAAT[A/G]ATTCCATGATTTCTT | 114792 |
| rs764335618 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002387 | ATTTCAAGAAAAAAG[C/T]ATAATTTAAAAATAT | 114792 |
| rs764349976 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121713 | CCCCTTTGTTTAGAT[G/T]ATTGTTTTGTGTCTA | 114792 |
| rs764354327 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096592 | TAGCCTGGCCTATTG[A/C]AGAATTTTTAATTCC | 114792 |
| rs764384423 | snp | A/C | 1.65031e-05 | 0.00287251 | missense, intron-variant, synonymous-codon, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113817 | AACACAACTGCCACT[A/C]CCAGTACATGGACGA | 114792 |
| rs764397828 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96925024 | GACCGCTCACCCCAT[C/T]GGGTAAGCCAGTCTC | 114792 |
| rs764437503 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007489 | TCTATGTGTCATTTG[A/C]GCCATTTCAGCCTGG | 114792 |
| rs764446170 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081949 | TTAGGATGTGAAGAT[C/T]GCAGTGCCCCGGTCA | 114792 |
| rs764464343 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97008953 | TAATTAATTAGAAGG[A/G]CAGTATAGTTTTAGA | 114792 |
| rs764467801 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120938 | GATGAAAACAAAGCT[A/G]CTCTAGTATTGAACT | 114792 |
| rs764472350 | snp | A/G | 1.87492e-05 | 0.00306174 | intron-variant | KLHL32 | GRCh38.p7 | 6:96975966 | GGGCTGGGAAAAGGA[A/G]AAATGTTGACTTGAT | 114792 |
| rs764482859 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064963 | CACCTTAGGTCCCCA[C/T]GACCATTGAGCAGCC | 114792 |
| rs764513864 | in-del | -/G | 1.6557e-05 | 0.00287719 | intron-variant | KLHL32 | GRCh38.p7 | 6:97127513 | TAATGAATTTTAAAA[-/G]ATTCCAGAGTAATTA | 114792 |
| rs764514587 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074193 | CAAGGAATCATCTGA[A/G]TGGATGGCTAAAACA | 114792 |
| rs764527458 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97100292 | AATATGCTTTTTCAA[C/T]ATCAGTAGCCAGACT | 114792 |
| rs764536610 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97143070 | CCTTGCCATGGAAAC[A/G]TTCTAATTAAATTGA | 114792 |
| rs764559288 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96937540 | TCTCTGGGTGTGCCT[A/C]CACTGCCCTGTCCCC | 114792 |
| rs764575913 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996138 | CCACTCTGTAGGTTC[C/T]GGAAGCTGTTGTCTA | 114792 |
| rs764621326 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113336 | CACATATTTTCTTAC[A/G]TTACTCATATTGATA | 114792 |
| rs764622223 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929297 | TTTGCTCTTCACAGA[C/T]ATATTTGGCAAGTAA | 114792 |
| rs764633998 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122302 | CCATCATCTGTGTGG[A/G]TTCCTCAAGTATGAC | 114792 |
| rs764667244 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033892 | ATTATTTATTTATTT[C/T]GCTATTGAATTTTGA | 114792 |
| rs764687503 | snp | A/G | 6.59304e-05 | 0.00574116 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114408 | TGCCTACAGTTGAGC[A/G]ATATTGCCCCAAGAA | 114792 |
| rs764737678 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082613 | AGCAAGATTCCATCT[-/C]AAAAAAAAAAAATAA | 114792 |
| rs764755849 | in-del | -/TATAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138241 | TAACAGAGGCTGTGC[-/TATAT]AAGAAGAGAGAGGCC | 114792 |
| rs764759794 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965062 | TAGGGATACTCAATG[C/T]TTAACTCACTTAGAA | 114792 |
| rs764764259 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139160 | AAAGAAGAAGTATTC[C/T]ATGGGCCTACACTCC | 114792 |
| rs764771728 | snp | C/T | 1.64746e-05 | 0.00287002 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897815 | ATCTCCTCATAACAT[C/T]ATGCGCTCAGGTTCA | 114792 |
| rs764777717 | snp | C/T | 1.64838e-05 | 0.00287083 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085238 | ATCTCTCTGAACTCC[C/T]GAAGAGCCGCCCAGA | 114792 |
| rs764836850 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939625 | TGGGAAAAAATTCTA[C/G]GAGGAAACACAGTGT | 114792 |
| rs764854468 | snp | A/G | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139266 | AAGTGCCTCATCACA[A/G]GATTGGCACCATCTG | 114792 |
| rs764855299 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96984564 | TCTGGGTGCTCCTGT[A/G]TTGGGTGCATATATA | 114792 |
| rs764870074 | snp | A/G | 1.64743e-05 | 0.00287 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114105 | CTGTTGATCAGGAGA[A/G]TGCTCTCATAGCTGC | 114792 |
| rs764891759 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96940317 | ATCTCAAGGAACTGT[A/G]GCTCTTAATGATTAG | 114792 |
| rs764906922 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977472 | TGCCTATTTAATTTT[A/C]TTTTCAATGTTTTTT | 114792 |
| rs764944579 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97048226 | CCAGGCACTGCTAAC[A/T]CTGTCAGCTGTGAAC | 114792 |
| rs764963883 | snp | C/T | 1.64817e-05 | 0.00287064 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041507 | GCAATGTTCAGTCTT[C/T]GTATGGTGGAAAGTG | 114792 |
| rs764966401 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112136 | CCAGGCTTGAGGGTG[A/G]GGCCCTCAGTGGGGA | 114792 |
| rs764983800 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073711 | TCCTGACTAGGGAAC[A/G]TAAAAACTGTGTATT | 114792 |
| rs764990025 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066953 | CTTCAATCAATGCTG[A/T]TATATTCTCTATCTT | 114792 |
| rs765002016 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96999780 | TGCTTCTTTATTATG[G/T]TTCTTAATGTGGTAA | 114792 |
| rs765004514 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126520 | TGATTAGGTGGGTCT[C/G]AGGTCTCTTAGATCT | 114792 |
| rs765010853 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933845 | TGAAAATCTCTCACT[A/G]TTATTGCTTCTGTGG | 114792 |
| rs765037285 | in-del | -/AAGAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903879 | CAGCTCACAAAGAAC[-/AAGAA]AAGGAAATAAGAATT | 114792 |
| rs765050270 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052831 | TCTCTTTATTAACCT[C/T]CACTTTTTATGCAAT | 114792 |
| rs765054791 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089376 | TTCAGTAGTTAGGTT[A/G]AGGAAATTTATTTCA | 114792 |
| rs765061141 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964346 | CTATTTATGGTGAGA[A/G]AAACTTTTTATAAAA | 114792 |
| rs765079965 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900976 | GTGATGCAGTGTTTT[A/G]GGTCTGTAAAACCTA | 114792 |
| rs765092684 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117443 | CTTGACATTTCCAGC[A/G]TGCTCACTCCCTCTC | 114792 |
| rs765097019 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111412 | ACTGGAATGCGGGTG[C/T]TGGGGCTAGCCAGCC | 114792 |
| rs765100429 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960454 | ATAACTAGGGGCTCC[C/G]ACATGTATTTATGTT | 114792 |
| rs765102153 | snp | A/G | 1.64928e-05 | 0.00287161 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114230 | GAAGTTGAGCATGCC[A/G]GTGGCCGGACGTGTG | 114792 |
| rs765102960 | snp | A/G | | | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897986 | CCCAGGGCATTTAAA[A/G]GGGAGCCCCTCCCTT | 114792 |
| rs765146690 | in-del | -/TC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939319 | GGCATCTGTCAAGTG[-/TC]AGGCATTATGCCAAA | 114792 |
| rs765177663 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958701 | TTGGCTAGAACTGGA[A/T]CTTCACATCTCTCAG | 114792 |
| rs765182766 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932476 | CTTTTTTCTGAAATC[C/T]CTAAGATTTGTGAGT | 114792 |
| rs765187562 | snp | C/T | 4.95741e-05 | 0.00497841 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041590 | TCTGGAGTTTGCATA[C/T]ACAGGACAGGTATGG | 114792 |
| rs765195698 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102790 | TAGGACATTTTCGCC[A/G]TTTAAAAGTTTTGTA | 114792 |
| rs765218682 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031160 | TAGGCAACTGGTGTT[C/T]CACTGTACCAAATGG | 114792 |
| rs765250815 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113837 | TACATGGACGAGCTC[C/T]TGCAATACATCCGCT | 114792 |
| rs765256094 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057190 | TTTTTTTTTTTTTTT[G/T]TTTTTTTTTTTGAGA | 114792 |
| rs765257597 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018166 | CGAAACTTTTTTCAA[C/T]GCTACATACTTCTAA | 114792 |
| rs765280523 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071733 | ATTCCACTAAATAGT[A/G]TTGGTTTAGCCATTT | 114792 |
| rs765336094 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97012246 | GAAGTGATGGACCTT[A/G]AGGTGGCAATACTAT | 114792 |
| rs765339558 | snp | A/G | 1.64819e-05 | 0.00287066 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132721 | GGATATTCAATTTGG[A/G]CAAATGAGCCTCTGG | 114792 |
| rs765412289 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052564 | CAGGGCATTCCGGCG[C/T]GCAGGCTGTAGGTCA | 114792 |
| rs765432562 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978853 | TGACTGGTGTGAGAT[A/G]GTATCTCATTGTGGT | 114792 |
| rs765438289 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022094 | TTCTTCAATCCTTGA[A/T]GCTTTGGAGTCTGTT | 114792 |
| rs765453915 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916437 | GTCTGTAGGAACAAA[C/T]CTTACTAAAGCAACC | 114792 |
| rs765463794 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911381 | CCTAGAACCAACTCA[A/G]GCATTTTCAACTTCC | 114792 |
| rs765470949 | snp | A/C | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924328 | GCTGGGTTCCCGGGT[A/C]TCAGTCGCCGCAGTG | 114792 |
| rs765471854 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065935 | AAATACAGTTTATGG[A/G]ATTCTTATGATTATT | 114792 |
| rs765475172 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111031 | CCACAGAAAAGTCTT[-/G]GGGGGGGGGGGTCTT | 114792 |
| rs765478428 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032825 | CATTTTATAAACTAA[A/G]GGTTTTTATTTAACT | 114792 |
| rs765487836 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97023202 | ACTAAATACATATAA[C/T]TTAGAAATTGTAAAG | 114792 |
| rs765518918 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936202 | TAATCCAATGACTAA[C/G]GATAAAGAATGCTAA | 114792 |
| rs765565412 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088295 | AGATGAAAGACACCA[A/C]ATTGACTATTGGGTT | 114792 |
| rs765575566 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961142 | GGGTTAAAATATTTT[G/T]ATTTCCTTCTTTATC | 114792 |
| rs765582470 | snp | A/G | 4.98202e-05 | 0.00499075 | missense, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976100 | GATGGCATCCTCTGC[A/G]ACATCACCCTGATTG | 114792 |
| rs765587241 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109010 | GCCTGATAGGAGAAT[A/G]CTGTTATGAATGGAA | 114792 |
| rs765610972 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979911 | CTAGGTATTTTATTC[G/T]TTTTGTGACTATTGT | 114792 |
| rs765649352 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96903443 | TTACATTATATAAGA[C/G]CACCTTAGGAGACAA | 114792 |
| rs765666215 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932362 | TCATTTCTTGGAGGT[A/G]TTCAAGATCACCTAC | 114792 |
| rs765674298 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902437 | CTTTGCATACTTTTT[A/G]ATTGGATTATTTGTT | 114792 |
| rs765677043 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96948442 | ATCAGATGATTCCTG[A/C]GACCTACAGAAAAAT | 114792 |
| rs765692950 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917048 | CTATGTATACTTTAT[A/G]TAAGCACTTTTCACA | 114792 |
| rs765699894 | in-del | -/TGGTGA | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009192 | ATGGTTTACTAGTAT[-/TGGTGA]TGGTATCTAGTTTTC | 114792 |
| rs765716114 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119323 | AAAACCCCCTCTTCT[C/T]AGACTCAGAGAGAAG | 114792 |
| rs765722005 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103697 | GTTCTCTGCATTGGC[A/C]CCACGTGCATGTGCA | 114792 |
| rs765730275 | in-del | -/TTCG | 1.64749e-05 | 0.00287005 | frameshift-variant, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114074 | GCAAGGTCAAGGAAC[-/TTCG]TTCGGTACTTCAATC | 114792 |
| rs765741796 | snp | A/G | 1.78449e-05 | 0.00298699 | intron-variant, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114597 | ATACTGTGGCCATGT[A/G]TAATTGAAAGATTGA | 114792 |
| rs765765037 | snp | C/T | 1.67818e-05 | 0.00289665 | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139293 | TCTGAAAAGCCAAGC[C/T]ATCATGAACAGGAGG | 114792 |
| rs765804534 | snp | C/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082481 | AGCCGGGCATGGTGG[C/G/T]GGGCGCCTGTAGTCC | 114792 |
| rs765823771 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97133726 | TCTTGACAGAGGTTT[A/G]TCTGGGGAATTTAAA | 114792 |
| rs765833916 | snp | C/T | 1.7403e-05 | 0.00294978 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085081 | TGCTCTTTCTCGGAT[C/T]TATTTCTAAGAGATC | 114792 |
| rs765886035 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926752 | AGCTCCCACTCCACT[A/G]TAGCCGATTGTTACT | 114792 |
| rs765899292 | snp | A/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998428 | ATCTCTTTTTCAGAA[A/T]AAGAATTAATAAAAA | 114792 |
| rs765909118 | in-del | -/GC | | | frameshift-variant, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114206 | GACTTCCTGTTTGTG[-/GC]AGGAGGGGAAGTTGA | 114792 |
| rs765933181 | snp | A/G | 1.64749e-05 | 0.00287005 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897820 | CTCATAACATTATGC[A/G]CTCAGGTTCAGGCCG | 114792 |
| rs765976112 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96964901 | CATGTACATGTGTAA[A/G]TTTGTTACATGGGTA | 114792 |
| rs765980063 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96908385 | TGATAAAACTGGGCT[C/T]GCCTAATGATTTGGC | 114792 |
| rs765981133 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918654 | ATTTAAATTCCATGA[C/T]AAGTGGCCTAAACAT | 114792 |
| rs765987618 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092707 | TCTTTCCTTCTAATC[-/TA]TATATGCGGCTAACT | 114792 |
| rs766020305 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036797 | GGGTGCCAGAGTGGC[A/C]CCCTCCAGCTCCAGG | 114792 |
| rs766043269 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071001 | TTCTGCTCCTTATTC[C/T]ATCAGTTACGCCCTG | 114792 |
| rs766046323 | snp | C/T | | | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898068 | GCTTAAGTCCCCAGA[C/T]CCACGGTTGCTTTTA | 114792 |
| rs766055467 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103473 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 114792 |
| rs766058041 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97091175 | GATTGCACCACTGCT[C/G]TCCAGCCTGGGCAAT | 114792 |
| rs766064576 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997406 | CCACATATGTATGCA[C/T]TGGTTAAGACATTAG | 114792 |
| rs766070241 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004939 | CTGAAGTTTTCTTTC[-/T]TTTTTTTTTTGTTAT | 114792 |
| rs766082134 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967426 | ATATATGTGTGTGTG[-/TA]TATATATATATAGAT | 114792 |
| rs766093948 | in-del | -/AGT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004928 | AGGCTATTGGCCTGA[-/AGT]AGTTTTCTTTCTTTT | 114792 |
| rs766097524 | snp | C/T | 1.64882e-05 | 0.00287121 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114353 | GCCATGGAGGAATAC[C/T]TCTATGCAGTTGGGG | 114792 |
| rs766099552 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059226 | AGGATTTTGACATAT[A/G]GAAATTAAAGGAATG | 114792 |
| rs766109074 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97124241 | GCACTAGGTTTGTTA[C/G]GCACCTCCTGTGGTT | 114792 |
| rs766114628 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896723 | TAAATTGTGTATTCA[C/G]TTAATTAAACACACA | 114792 |
| rs766130620 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076553 | CCTACAGCTCTAAAC[C/T]AAAGACACCACCAGT | 114792 |
| rs766146134 | in-del | -/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97068139 | CATCAGAAGCTTTGA[-/TG]TGAAGATGTCTCTTT | 114792 |
| rs766147748 | snp | C/T | | | upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897966 | GGCCACACACCGCTT[C/T]TCTGCCCAGGGCATT | 114792 |
| rs766155790 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898786 | CTGTAGTGCTGCTTT[C/T]ATTTAAGACCCTTTA | 114792 |
| rs766162728 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943348 | CACACAAGACCTGTG[C/T]GGTAATATGATATTT | 114792 |
| rs766212209 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96932083 | AGGAGACTTTCTCTT[A/T]AAAAAAATACTGTTT | 114792 |
| rs766222654 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047358 | TCATGGGTGTCCTTG[C/G]ACAGCCATGCATGGA | 114792 |
| rs766223812 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030097 | CCTGTAAGATTATTT[A/G]TATTCTTGATAAAAT | 114792 |
| rs766225547 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044169 | ATATACATTCTTTCT[A/G]TGCCTAACTTGTTGA | 114792 |
| rs766240958 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114998 | TGAGAGAAGGGATTT[A/C]AGTTACCAAAACAAA | 114792 |
| rs766285363 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002171 | AAGTCCAAAGGTAGG[A/T]TAAGAACAATGTTCC | 114792 |
| rs766312230 | snp | C/T | 1.65261e-05 | 0.0028745 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896805 | AGAAACGACAGCAGC[C/T]TTTCATCTTTACGAG | 114792 |
| rs766326208 | snp | A/C | 1.69444e-05 | 0.00291066 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130990 | AGGAAAAGTAGATTC[A/C]AGAAGTCACCAAACT | 114792 |
| rs766335480 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97092733 | TAACTCCTCTGTGAG[A/G]GTGCATCCCACAGTA | 114792 |
| rs766348970 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070312 | CCTATTAAATCATAG[A/C]CAACTAGTAATTATT | 114792 |
| rs766368790 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939323 | TCTGTCAAGTGTCAG[G/T]CATTATGCCAAAGGC | 114792 |
| rs766371891 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090913 | CAATTAATCCTATGA[C/G]TTTAACAGGAATTAA | 114792 |
| rs766374294 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010445 | AAATATTTTTTAAAA[C/T]ATTTATCAGCATCAT | 114792 |
| rs766387215 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029263 | GAGCTCATTATCACT[A/G]TATAGTTAATTTAGG | 114792 |
| rs766396535 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97020212 | TCCCAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 114792 |
| rs766408157 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96991291 | GGGGGTGGGGTGTCT[C/G]CTCTGCAATTCCAGC | 114792 |
| rs766421547 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921527 | TCAATTTTGGTTTTG[C/G]CATAATTAATGCTGC | 114792 |
| rs766448800 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97107616 | CCAAGAATCTCAAAT[A/G]GAAGTGGCCAACACC | 114792 |
| rs766459817 | in-del | -/GT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131084 | TTATTAACCAGAAAG[-/GT]GTGTGTATCATTTAT | 114792 |
| rs766493698 | in-del | -/ACAAAAAAA | | | intron-variant, cds-indel, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010125 | TCAGGCACTGATTTG[-/ACAAAAAAA]AAAAAAAAAAAAAAA | 114792 |
| rs766496525 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97009524 | ACTTTGAAATGTTTG[A/G]AAAGTTGTGTATGGA | 114792 |
| rs766496536 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030439 | ACCTCCCTCTGTGGT[A/G]GGCACTTAAAGTGGA | 114792 |
| rs766504500 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113968 | ATACCACCAGAGCAT[C/G]TATGCACAGCCTGTC | 114792 |
| rs766528137 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106252 | ATATGATTAAATTGC[A/C]TATTTTAATTGAACT | 114792 |
| rs766534691 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094757 | TAGGAAGAGTTACAA[C/G]TCAGTATTGGTAAGT | 114792 |
| rs766546047 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951507 | GCGCCACCCCACACC[C/T]TGTACCTTAACCATC | 114792 |
| rs766556061 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916285 | TATTGTTATAGGCAC[A/C]TACTCCTAAGTTAGG | 114792 |
| rs766556104 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032648 | TGGTGGCAAGCAGGC[C/T]GTCAGCACATCAGGG | 114792 |
| rs766561211 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103022 | AAGGTATATTTACCT[A/C]TACGAGGTAAATAAA | 114792 |
| rs766577335 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96995071 | CTTCTGTGAACCTAT[G/T]TTTTTTCATCTATAC | 114792 |
| rs766584010 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960059 | CAGTAAATTCCTTGA[C/T]CTCATTATGCCTTAT | 114792 |
| rs766593882 | snp | A/G | 1.65075e-05 | 0.00287289 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041454 | GCTCCCTTGCTGTCA[A/G]AGTCTCATAACTGTC | 114792 |
| rs766619136 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936097 | CTTTTTGTTGGTCAG[C/T]TGGGGCCAGCAGTAG | 114792 |
| rs766627031 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97050646 | CATTCTACTTGAGTA[A/G]TAGTCACATTTCAGG | 114792 |
| rs766630338 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958877 | ATGCAGGTGCACACA[C/T]AGCTTGGCCTCAGGG | 114792 |
| rs766645626 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119185 | GGAGGACAATTAGCA[A/G]GAGGGCTTGGTATGG | 114792 |
| rs766645719 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131191 | TCCTCATATGGCTGA[C/G]AGGCATGTCAAGTCC | 114792 |
| rs766668627 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040379 | TTTAATTTCAAATTT[C/T]CATTTGACATACTGA | 114792 |
| rs766668644 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956783 | TAAGTGTATTAGCAC[A/G]TGTACATACATACGC | 114792 |
| rs766683274 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97022670 | AGATGGGGTTTCATC[A/G]TGTTGGCCAGGCTGG | 114792 |
| rs766704119 | snp | C/T | 1.65433e-05 | 0.002876 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130777 | GTGGATAAGCCGTAG[C/T]CCCATGCTGCAGAGA | 114792 |
| rs766707529 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084767 | TTTAGTAGAGAAAAA[C/G]CTGTAAAATATGGTA | 114792 |
| rs766723474 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946606 | AGGAACAAGGGCCTG[G/T]ATAATTATTTTATAA | 114792 |
| rs766731769 | in-del | -/GCCAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057187 | TTTTTTTTTTTTTTT[-/GCCAC]TTTTTTTTTTTTTTG | 114792 |
| rs766732303 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96905760 | AATTATAGTTTAGGT[C/T]TGATTGGCACTTTAT | 114792 |
| rs766733348 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061319 | TTTGGCTTCTTTTAG[A/G]GTTTCCTTTCCCCCC | 114792 |
| rs766734953 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971773 | CCCTGGGAACTCATA[A/G]AGTATCCAATAGAAC | 114792 |
| rs766764029 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029108 | ACCATAACTTTGGCT[-/A]AAGAAACAACTTGAT | 114792 |
| rs766789856 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026211 | CCATTTTTATAAGAT[A/G]TAGAGACTTTGTGTT | 114792 |
| rs766795841 | snp | C/T | 1.66294e-05 | 0.00288347 | splice-donor-variant, intron-variant | KLHL32 | GRCh38.p7 | 6:97085343 | AGCAGATCTGGCAGG[C/T]AAGGGCGCTGTGCAC | 114792 |
| rs766811722 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097611 | TCTTTCACTCGGTGA[C/T]CTTCACAGCAGCTTT | 114792 |
| rs766818945 | snp | A/G | 3.29674e-05 | 0.00405988 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085247 | AACTCCTGAAGAGCC[A/G]CCCAGAAGAAGTTCT | 114792 |
| rs766821629 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939548 | AGCCTTCCCTAAGGG[A/G]GTTTGAAGGACATGA | 114792 |
| rs766827035 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96929533 | TTTACTTTCTCTGTT[G/T]TTGAGAATTAGTAAA | 114792 |
| rs766881973 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004281 | GCTTTCAGCTTGGAC[A/G]TTGTTGGTGTATAGA | 114792 |
| rs766897416 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926520 | AACCCAAGACTCAAA[A/C]CTTGCTGAAGGTCAC | 114792 |
| rs766898958 | snp | C/T | 3.29951e-05 | 0.00406159 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114258 | GTGCTGTGAGGACTG[C/T]CTGTCGCTATGACCC | 114792 |
| rs766919776 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137448 | TTCTTTTATTCTAGG[A/G]CTTCTTAGTAATTTC | 114792 |
| rs766928226 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986640 | TGTGCTAGCAATGAG[C/T]GAGGCTTCGTGGGTG | 114792 |
| rs766938338 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060746 | ACCAGGAGGGTGATT[G/T]GGCCACCTCATGACT | 114792 |
| rs766988513 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931941 | CTACTCCCCAAGCAA[C/T]AGTTATGGTTATTAT | 114792 |
| rs766993935 | snp | C/G | 1.64735e-05 | 0.00286993 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897783 | AATTCCTGATACCGC[C/G]AATCACTAGTGCTCC | 114792 |
| rs766997807 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97122861 | TTAATGCCACAGCCT[A/G]TCCTGAAACTCTTCC | 114792 |
| rs767001282 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97076103 | AGAGCTTGAGAACCA[A/G]AGTATATTATAGTAA | 114792 |
| rs767010601 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067833 | CCTCCCTGGCTTCAT[C/T]TCCAGCCACTGTGCC | 114792 |
| rs767029687 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074489 | TGCTTCATAGCATCC[A/G]AAAGATAAAAAGCGA | 114792 |
| rs767030751 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130870 | AGACTACAATAATGA[C/G]CGGATCCTTGTGCGC | 114792 |
| rs767045031 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015141 | TCCTGAGGCCTCCCT[A/T]GCCATGTGCAACTGT | 114792 |
| rs767047037 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96996286 | GACATTTTGGAAAAT[C/T]AAATATTTGAGCATC | 114792 |
| rs767118026 | in-del | -/AC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96920573 | AACACACACAATTAC[-/AC]ACACACACACACACA | 114792 |
| rs767134572 | snp | A/C | 1.64754e-05 | 0.00287009 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897833 | GCGCTCAGGTTCAGG[A/C]CGCACGTGGGAACAC | 114792 |
| rs767153157 | snp | A/G | 6.59881e-05 | 0.00574367 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97064690 | TCACCTACAGCTGTT[A/G]GAGCTTCTCAATTTA | 114792 |
| rs767164689 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081561 | CCACCCTTTGCCAAG[A/T]GAACAAAGGATGCTC | 114792 |
| rs767168328 | in-del | -/CCG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97056252 | TGGGACTACAGGCGC[-/CCG]CCGCCACCACGCCCG | 114792 |
| rs767178670 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97059167 | GAGAGATCTTGCCAA[G/T]CTTTGTATAAGGAGT | 114792 |
| rs767192876 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029947 | AGATGTAAGATGTAA[A/C/T]GGATCTACTGTAATC | 114792 |
| rs767207783 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114881 | GGCTACCTGACTAGA[A/G]CCATTTCATCAAAGA | 114792 |
| rs767208106 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007071 | TTTTCATGAAAGATA[C/T]CTTTAAATATGTTTT | 114792 |
| rs767222167 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029080 | GTGAGCAGCAGTTTC[C/T]GGCCTTCACAATTAC | 114792 |
| rs767225005 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102768 | GGTGCTGTTTTTTAT[C/T]GTCCTGTAGGACATT | 114792 |
| rs767235720 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135799 | TATGTTATGGATGAC[A/G]ATAGAACAATTGGTT | 114792 |
| rs767246783 | in-del | -/TATAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97037090 | TCAAATATAATTGAA[-/TATAT]TATATGTTAAATACT | 114792 |
| rs767256509 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97116878 | AAATACATTTTCTTT[C/G]TTCTTCTTTTGCACT | 114792 |
| rs767262271 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97057107 | AGAAATTAATACCCC[A/C]AAAATTAAACAGGCG | 114792 |
| rs767281286 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96912346 | AACCACCAAACAGAT[A/G]AACCTTGCTTCTCAG | 114792 |
| rs767285207 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058563 | ATCTAGCCATAAAAA[C/T]TTAATTTCCCAGGCT | 114792 |
| rs767285850 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96956164 | TCACTATCACGAGAA[C/G]AGCATGAGAAAGACC | 114792 |
| rs767306972 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97088854 | TCATTTCCATAGGAA[G/T]TGCTGAGTAAGCTCT | 114792 |
| rs767330031 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97002897 | CCTTTATTTAGTCTA[C/T]TGTTAATGGGCATTT | 114792 |
| rs767332980 | snp | C/T | 1.65669e-05 | 0.00287805 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897668 | TCGCACCACTCACGA[C/T]TAATCTGCTCTCGCA | 114792 |
| rs767363590 | snp | A/G | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896360 | ACACCACTTACTAAA[A/G]GAGTCTCTGAGATTA | 114792 |
| rs767400106 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128215 | TTGGGACTGGCCACC[A/G]AATCTATGTCCCTAG | 114792 |
| rs767400435 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97142733 | AGAAGCTTGTCAAAT[G/T]TTTATATAACATACA | 114792 |
| rs767404214 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131792 | TTTAGATGCTTGTAT[G/T]GAGCTCCTGTTTTTG | 114792 |
| rs767434532 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915013 | TCCTGGACAATTTCA[A/G]TGACCCTTCCTCCAA | 114792 |
| rs767439806 | in-del | -/GGAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96975568 | TGGGGAAGGAATCAG[-/GGAA]GGAATTAGAGAGAGG | 114792 |
| rs767444468 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127167 | GTCAGAATTGGGGTC[C/T]TCTTGGTAATGTCAG | 114792 |
| rs767447137 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031326 | TTTAAAAATTATAAG[A/C]ATTAAGTTTTTAACA | 114792 |
| rs767447782 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990242 | TTCACAGTTACAATT[C/T]GAGTACATTCAGTTG | 114792 |
| rs767450348 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979767 | GTATGGCCATTTTCA[C/T]GACATTGATTCTTCC | 114792 |
| rs767454019 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104604 | ATTTGGTTCCATTGA[A/C]ATATATTTCTTAGAA | 114792 |
| rs767462244 | snp | C/T | 1.64849e-05 | 0.00287092 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97132730 | ATTTGGACAAATGAG[C/T]CTCTGGCTTGTATCC | 114792 |
| rs767500316 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019045 | AGTACATAATTGGAC[A/G]TAAAGGACTCATTAA | 114792 |
| rs767511038 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97070611 | TGACTGTATCTTCGT[C/T]TGTGAGGATTTTAAA | 114792 |
| rs767522895 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952926 | CTGTCCCAGCACATA[-/C]AGGATTGTTTACCAC | 114792 |
| rs767524316 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96922121 | TAGTGAATATATGCT[A/G]TTTTCCAGCCACCCA | 114792 |
| rs767530683 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96933916 | GAGAGCAAAAGCAGG[C/T]GGAATCAGTTTCCTT | 114792 |
| rs767534032 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97051647 | GTTCCTTCTTGATCA[A/T]GTGAATTTCTGAGTG | 114792 |
| rs767536284 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97113716 | CAGGTAACCTACCTA[C/T]ATGCTGTTGCTTTCT | 114792 |
| rs767549964 | snp | A/G | 3.31807e-05 | 0.00407299 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139134 | AGGTACTGGATGTAA[A/G]CAGAGAAGGCAAAGA | 114792 |
| rs767552131 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97113849 | CTCCTGCAATACATC[C/T]GCTTTGGCCTAATGG | 114792 |
| rs767557249 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901212 | TGCTAGCAAATTACC[A/G]CAAATGGTTTAAAAC | 114792 |
| rs767579278 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96899682 | CATCAGAAACTCACA[A/T]TTGGCTGTCACCCTT | 114792 |
| rs767606823 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028546 | TCTAAATAAATTTCC[-/T]TTTTTTCATATTTTC | 114792 |
| rs767625250 | snp | C/G/T | 3.8396e-05 | 0.00438142 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130706 | ACTCGTTGCTGTTTT[C/G/T]TGACATGGAGGTCTC | 114792 |
| rs767628284 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97119048 | CCTCCCTGTCCTCAC[A/G]CTTGAACTTCATGGT | 114792 |
| rs767648378 | snp | A/C | 4.94678e-05 | 0.00497307 | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97041485 | TTTCTCCCTTTCCTC[A/C]CCTCAGGCAATGTTC | 114792 |
| rs767656209 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071858 | TCAGCTGCGCTCCCT[G/T]CCTGTAGTCTAATGC | 114792 |
| rs767674002 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004177 | TGTTTTGTAAATCTT[C/G]TAGAGATCTTTCACC | 114792 |
| rs767679957 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117599 | ATTTAATTAAAGATG[G/T]TAGAGTCGAATTGTA | 114792 |
| rs767696616 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97042460 | AAGAATGTGTGGGAG[C/T]TCATTTTTCTACTGA | 114792 |
| rs767717114 | snp | C/T | 3.29712e-05 | 0.00406011 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130804 | GAGAAGGGTCTACCA[C/T]TCCATGGCTGCTGTA | 114792 |
| rs767720165 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97003043 | ATTGCGGGTCAAATG[G/T]TAGTTCTAAGTTCTT | 114792 |
| rs767740914 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970726 | TCCTTTCTACAGAGT[A/T]TTCATTATTTAATAA | 114792 |
| rs767744509 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946546 | TGTCACTTCACTGCT[A/G]TGAGCTAGGAATTAT | 114792 |
| rs767753750 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969298 | CCATTTTACTCTTAC[C/T]ACAGCCTCCTCTCCT | 114792 |
| rs767762077 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927920 | TCCATATCGGCTTCA[C/G]AATGACTCTATAAAG | 114792 |
| rs767772974 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061272 | CCCAAGCAGGTGAGC[A/G]TCACTGGGGGTAGAG | 114792 |
| rs767805300 | snp | G/T | 1.66007e-05 | 0.00288098 | synonymous-codon, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130948 | TTTCAACCTGCTGAC[G/T]GGCAAGTACCTTTGA | 114792 |
| rs767816439 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913738 | GTGGCCTGGATCAGA[A/C]TATTGCCAGGCTTTC | 114792 |
| rs767822491 | in-del | -/AGAC | | | utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139815 | GATACGAATAATAAT[-/AGAC]AGACATACACTGGAA | 114792 |
| rs767827077 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97099079 | CTCATTTTGTCAAAT[G/T]GTTTCTGGTCTAAGC | 114792 |
| rs767833095 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030861 | TATGACACTGTAGGG[-/T]TGGTAGGACATCATC | 114792 |
| rs767838961 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014966 | TGATTGAATCATGGC[A/G]GTGGTTTCCCCCATG | 114792 |
| rs767853313 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958797 | ACTAGTGGGTTACCC[A/G]TGGAAGGTAGCTGGG | 114792 |
| rs767857159 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97084597 | TTCCTGAGACCTTGT[A/G]TATAAAACTCTGGAT | 114792 |
| rs767857383 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071314 | AGTGACTCCTCTACA[G/T]CATTTAAACACCGGG | 114792 |
| rs767857619 | snp | C/T | 3.40681e-05 | 0.00412709 | intron-variant | KLHL32 | GRCh38.p7 | 6:97085358 | TAAGGGCGCTGTGCA[C/T]GGTCGCTTTTGGCAC | 114792 |
| rs767880645 | snp | A/G | 3.33795e-05 | 0.00408517 | utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96967039 | CTTCTAAGGCTGAGA[A/G]CCTGAGGAACCCAGC | 114792 |
| rs767882087 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97066199 | TTACGCATCATCACC[C/T]GATTCACTTTCCCCA | 114792 |
| rs767882634 | in-del | -/TA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967425 | ATATATGTGTGTGTG[-/TA]TATATATATATATAG | 114792 |
| rs767894746 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097549 | ACTCTGGAAATCACA[A/T]TTTATTTTTTCCTTG | 114792 |
| rs767897910 | snp | A/C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97132065 | CTTTCATCATTTTGG[A/C/T]GTGTCAGCATCTAGG | 114792 |
| rs767898464 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944431 | TAAGGAATGCTGTTT[C/G]TGGGGAACAAATTAG | 114792 |
| rs767907344 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036128 | GTATTGAAGTTCTCT[A/G]TCGCATTTTTTTATT | 114792 |
| rs767913971 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96926313 | AGAGTGTAATAAATA[A/G]TGTGAGGAGCAAGTA | 114792 |
| rs767921827 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065033 | CCGGGGGAGGTGTCG[C/T]TAAAAGGAGTCCTAG | 114792 |
| rs767922998 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96988281 | AAACAACCCCATCCA[-/C]AAGTGGGTGAAGGAT | 114792 |
| rs767943188 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071449 | TCCCTCAAAGCATGG[C/G]AGCTCTGCATGGGCA | 114792 |
| rs767948661 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97109359 | AATGTTGGAAAGAAA[C/T]AAGATAAAAATATCT | 114792 |
| rs767951358 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97074396 | TAAGTCACTGATATT[C/T]AGATTTTGAAAGTGT | 114792 |
| rs767955103 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96997265 | TTTGTACCCTAGAAC[C/T]CACAGTGCCTGGCCC | 114792 |
| rs767955725 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013640 | AAAGGATAAAATAAC[A/T]TTTAGTAAACAGCCT | 114792 |
| rs767970476 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916371 | TATAGAAGTACAGTC[-/T]TTTCTCAGGACATAT | 114792 |
| rs767978728 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96981653 | ATGTTAGATTGTTAA[C/T]GTGACATCTTTCTAA | 114792 |
| rs767988747 | snp | C/G | | | upstream-variant-2KB, intron-variant | KLHL32 | GRCh38.p7 | 6:96924146 | CTGGTCAGTACCATA[C/G]AGTGTATTATCCTAA | 114792 |
| rs767996906 | in-del | -/AAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910999 | GTTAATTGTGTAAAT[-/AAC]ATAATAATACATATC | 114792 |
| rs768006654 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129749 | CAGCCAGGTTTGGTG[A/G]CACTTGCCTGTAATC | 114792 |
| rs768008643 | in-del | -/ATTGATC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093991 | GAACAAATGGAAATG[-/ATTGATC]ATTGATCATTCCATC | 114792 |
| rs768029236 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96950204 | GCAAGTGTTTTTGGA[A/G]GTGTCTGAAATTTCT | 114792 |
| rs768038531 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110293 | GCATCTAGAGTGTAT[C/T]GCTTGTTTGACCTCT | 114792 |
| rs768079601 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998140 | CTCCAGTATACTTCC[A/G]GTAAATTATCCTTTT | 114792 |
| rs768096368 | in-del | -/TGTCGCTCCCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085915 | ATTCTTTTCACATTG[-/TGTCGCTCCCT]TGTCTAGAGGACAGG | 114792 |
| rs768098234 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96969000 | TTCTGAAGATGATGC[C/G]CTTTATCTCTCTCCT | 114792 |
| rs768099371 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942800 | TATTCTGATGCCACC[A/G]CCTCCCTTTCTACCT | 114792 |
| rs768114264 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082441 | ACACGGTGAAACCCC[A/G]TTTCCACTAAAAATA | 114792 |
| rs768154125 | in-del | -/TTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901329 | TTCCTCCTGGATGCC[-/TTTT]TTTTTTTTTTACTTT | 114792 |
| rs768155408 | snp | A/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897447 | GCTGCTGCCTCTGGG[A/T]CTCGGAAGTAGGCGG | 114792 |
| rs768157123 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96913044 | TGATTGCTCTCTGTT[G/T]CTGCTAAGTCACCAC | 114792 |
| rs768177433 | in-del | -/GA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967501 | AGGGATAGAGAATGA[-/GA]GAGAGAGAGAGAGAG | 114792 |
| rs768191560 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97052251 | ATGATTGGGACAGCA[G/T]ATGCACATGCAGATG | 114792 |
| rs768224529 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943842 | ACGAGTGTGCAGATG[C/T]ATTCTTTTTATAATT | 114792 |
| rs768246443 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040762 | ATGGAGGGTAATTGG[A/G]TCATGGGGGCGATTT | 114792 |
| rs768247426 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115651 | CATCACATTATAAAC[A/G]TGTGTTTTCAATCTT | 114792 |
| rs768249147 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96980868 | AGACTGGGTAATTTA[A/T]AAAGGAAAGAGATTT | 114792 |
| rs768253613 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123848 | AATCAGCTTGATGAC[-/T]TTCAAAGCCAGGAAT | 114792 |
| rs768255383 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96967382 | TATAAAGGTATATCA[C/T]ATAAAAAAGGAATCA | 114792 |
| rs768263680 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060568 | CTCCTCCTCTTTCAC[C/T]GGATTCTGGCCCCAT | 114792 |
| rs768265180 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96935938 | TGAATTTTGGTCCTT[C/T]TATGTGGTGCTTCTT | 114792 |
| rs768284865 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128082 | TTTGCCATTTCTATG[A/G]TTTTGGTAATGTAAA | 114792 |
| rs768291776 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904225 | TGCACATCGATAATC[C/T]CAGCTGCTCAGGAGG | 114792 |
| rs768300638 | snp | A/C | 1.64876e-05 | 0.00287116 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97127455 | TAATGGTGTATGAAC[A/C]TAACCAGGTAAGAAT | 114792 |
| rs768306447 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97096944 | AACAGCACTGAGAGG[G/T]TAGGTCATTGGAAGC | 114792 |
| rs768335565 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117036 | GAAAGAAGAGGAAAT[C/T]GCCAGTGACATTTCT | 114792 |
| rs768337143 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082614 | CAAGATTCCATCTCA[-/A]AAAAAAAAAAATAAA | 114792 |
| rs768354555 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039689 | GCCAGGAGTGGTGGC[A/G]GGCACCTATAGTCCC | 114792 |
| rs768355760 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936835 | CTGCCTTAGAACTGG[G/T]GTCTCACAGTTGGTA | 114792 |
| rs768363200 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97054310 | GTATACTTCATAAAA[A/G]CCATCCATTTACATT | 114792 |
| rs768383583 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928076 | CTAATGCAGGTTATA[G/T]ACATGTACATAATTG | 114792 |
| rs768388704 | snp | C/T | 1.72659e-05 | 0.00293814 | intron-variant | KLHL32 | GRCh38.p7 | 6:97130750 | ACACTTAAATTTCTT[C/T]TTTCAGAATAAGTGG | 114792 |
| rs768410516 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979700 | AATTCTGTGAAAAAC[A/G]TCATTGGTAGTTTGA | 114792 |
| rs768411951 | snp | C/T | 1.6501e-05 | 0.00287232 | missense, utr-variant-5-prime, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97085313 | AGAGCGACCGCCTGA[C/T]CTCCCTGAGTGAAGA | 114792 |
| rs768426462 | snp | C/T | 1.64784e-05 | 0.00287035 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897849 | CGCACGTGGGAACAC[C/T]GGCGCAGGACAACTC | 114792 |
| rs768453225 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916838 | TTCTTTCCTTCCTAC[A/C]CGTTTATAGTGCTAT | 114792 |
| rs768456260 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910194 | TTGGGAACAGGGAGT[C/G]GCACAGGGAGGTCCC | 114792 |
| rs768471106 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97108589 | TTCTTTGCCATTTTT[A/T]AATTATTTATTTGAA | 114792 |
| rs768487003 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120812 | TGAATTAGAATGTCC[A/G]TGAAGAATTAAATCT | 114792 |
| rs768491144 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97001934 | GAGAGAAATCAGACA[C/G]TGATTGAGTGTGAGT | 114792 |
| rs768499691 | snp | C/G | 1.64738e-05 | 0.00286995 | upstream-variant-2KB, utr-variant-5-prime | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897804 | CTAGTGCTCCCATCT[C/G]CTCATAACATTATGC | 114792 |
| rs768501140 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96949179 | GTGAAAATAGGGACA[A/T]TGCATGTCTTGTTTT | 114792 |
| rs768528805 | in-del | -/AGA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081159 | GGTTGGTGAGGAGGT[-/AGA]AGGAGTGAGGGGGGA | 114792 |
| rs768536694 | in-del | -/A | 1.67321e-05 | 0.00289236 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967127 | CCGTAGTGAGCCCTG[-/A]AAATAAGTGCATTGC | 114792 |
| rs768550966 | in-del | -/AT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96972825 | CATTTTAATTTAGAC[-/AT]AGTGCATTACAGTCT | 114792 |
| rs768572895 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046304 | TGAATTGACTAAGAT[C/G]ATTCTCTCATATATT | 114792 |
| rs768580346 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986284 | CAGTCTGCCCCTAAT[-/G]GGGGGGGGCCTCCCA | 114792 |
| rs768590665 | snp | A/G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97064395 | CAGAGCTTCACACAC[A/G/T]CAAATGGTATCAGCA | 114792 |
| rs768627772 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97034543 | TTTTTCTATTTCTAT[A/G]AAGAATGCCACTTGA | 114792 |
| rs768638879 | in-del | -/TC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97044992 | CTATTGTCTTTGTAG[-/TC]TCTATTTTTCACTAA | 114792 |
| rs768641113 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97026810 | CTAAGATAATAAGTG[A/G]TAACTGAGGAAATTC | 114792 |
| rs768652435 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96939303 | TGGCACACAGTTACT[C/G]GGCATCTGTCAAGTG | 114792 |
| rs768675584 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97025856 | AGTTGTGAAAATAAA[A/G]CTTTAATTCAAGTAG | 114792 |
| rs768683125 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97053866 | GATATTTTGTAGTCT[C/G]TGCATATACTACACA | 114792 |
| rs768696276 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96997970 | TCATTACCATTTCTG[C/T]TTCTCAGAAATCACA | 114792 |
| rs768701964 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075716 | AACCTTTCCTGCAGC[A/G]CCAGGTTAGGTAGTC | 114792 |
| rs768711934 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97061313 | ACCTAGTTTGGCTTC[-/T]TTTAGGGTTTCCTTT | 114792 |
| rs768723358 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101217 | ATAAAATGTATAAAT[A/G]TGCCAGCAACATTTA | 114792 |
| rs768733954 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018698 | AACATATGTGTAACA[A/G]TATTAATATGCTATA | 114792 |
| rs768735111 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96907896 | ACAACTAATAGCTCT[G/T]CTTTGTATGTGAATG | 114792 |
| rs768736906 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96909106 | AGACCAGCTGACTTC[C/T]GCTGCTGGATTTTTT | 114792 |
| rs768738238 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97055098 | CTCAGACAGATACCC[A/G]ATGCCAGGCAATGTT | 114792 |
| rs768752799 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962114 | TAGTTTGGAAGGCTT[A/G]ATCATGTTTCACTTG | 114792 |
| rs768756208 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97005403 | AGGTAGTGGTCTATC[C/T]CTCTTATTTATTCTT | 114792 |
| rs768781893 | snp | A/C/T | 3.31583e-05 | 0.00407164 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064753 | TGCATCCTGCTCATA[A/C/T]ACCCTTCACATTCCT | 114792 |
| rs768796220 | snp | A/G | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:96998267 | TCAGTCATCCACGCC[A/G]CAGCTTTCTTCTGGG | 114792 |
| rs768802092 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014646 | ATTTTGTCACTGTCC[A/G]TGCAACAGTTCTCTG | 114792 |
| rs768809295 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97040310 | TAGCATGGGGTTGTA[-/T]TTTTTTTTTTCCTTT | 114792 |
| rs768815931 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141867 | AAAATAATCTGTACA[A/G]TGCAATAACACTTCT | 114792 |
| rs768827715 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96986275 | TGTGAGGTGTCAGTC[C/T]GCCCCTAATGGGGGG | 114792 |
| rs768855988 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97090908 | GCATCCAATTAATCC[C/T]ATGACTTTAACAGGA | 114792 |
| rs768858162 | snp | A/C | 6.60982e-05 | 0.00574846 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896797 | CATCTTTTAGAAACG[A/C]CAGCAGCTTTTCATC | 114792 |
| rs768884303 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976653 | CCCAGGCTGGAGTGC[C/G]AATGGCGCAATCTTG | 114792 |
| rs768887509 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952751 | AAGGTGATCACAAGA[C/T]TTGTGACTTCCCCAG | 114792 |
| rs768891262 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97067727 | GATGTTGATCTGGCT[A/T]GAAAACTTTCATTAG | 114792 |
| rs768894674 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97121382 | AGCAGAGTGCTATCT[-/G]GGGATTTGTTTAGAA | 114792 |
| rs768908261 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97078434 | TTGGAAATGAAAGAT[G/T]ATAATTACATTGATG | 114792 |
| rs768939816 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077467 | AAGAGAAGTAAGCTT[A/C]TTTTTCAACATTCTG | 114792 |
| rs768957281 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97111393 | GACCCCTTCACGGGC[A/G]GGAACTGGAATGCGG | 114792 |
| rs768987051 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036741 | TAAGACAAGTGACAT[C/T]ACACCCAGGTGTGGG | 114792 |
| rs769002131 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123816 | GCAGCATGTGGCATC[A/G]TAACCCAGAGCAGAC | 114792 |
| rs769045027 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96951410 | GACTAATACTCAGAG[G/T]CAGGTGAGCAGTATG | 114792 |
| rs769049390 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96963463 | TTATAAATGTAAATT[C/T]TCTTTACAAAAGGAA | 114792 |
| rs769086070 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029955 | GATGTAATGGATCTA[C/G]TGTAATCATTGCGAG | 114792 |
| rs769087383 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96918167 | TGTCCAAGGCAGCCA[C/T]GTAGTCTCACTCGCA | 114792 |
| rs769092115 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97114777 | TGTTTTTTTCCTACC[-/A]GAACTTCTCCTGTCA | 114792 |
| rs769093472 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97047907 | GATAAGCCTTTAGAA[A/T]TTTGAGTACCTTAGG | 114792 |
| rs769094126 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017720 | AGTGACTTCACTTTC[C/T]AGTCCCACTTGTATC | 114792 |
| rs769095789 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030459 | CTTAAAGTGGATTAT[A/G]TACTCACAAACTAGG | 114792 |
| rs769123661 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936610 | TTCTTGTCCCAGTCA[A/G]CATTACCTGTTGCTT | 114792 |
| rs769126577 | snp | A/G | 3.31592e-05 | 0.00407167 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976081 | GCTGAATCAGCAGAG[A/G]AGTGATGGCATCCTC | 114792 |
| rs769134845 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898322 | GGAACTTACTGAACC[A/G]GGGTCAAACTGGGCT | 114792 |
| rs769135344 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96978774 | CAGCAGTGTATCAGC[A/G]TTCTCTTTTCTCTGC | 114792 |
| rs769159582 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123702 | TATCCTCCCTGGGGT[A/G]GGGGAGGGAGATCAA | 114792 |
| rs769194403 | in-del | -/A | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97129899 | AATACAAAACAAAAC[-/A]AAACAAAACAAAACT | 114792 |
| rs769197044 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007082 | GATATCTTTAAATAT[A/G]TTTTCTAAGTTGCTT | 114792 |
| rs769200140 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137276 | TTACCTAGTCAAAAC[A/T]ACTGTAAATGTGACA | 114792 |
| rs769211441 | snp | A/G | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130884 | ACCGGATCCTTGTGC[A/G]CCATATAGATTCTTA | 114792 |
| rs769213089 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089614 | TGAAACCCCATCTCC[A/G]CTAAAAATACAAAAA | 114792 |
| rs769214116 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96919136 | AGTGGAGTTATTTGG[A/G]TTCCTGGCTTTACAA | 114792 |
| rs769214420 | snp | A/G | 5.5622e-05 | 0.00527332 | intron-variant | KLHL32 | GRCh38.p7 | 6:96976202 | CATTGTTTGTTTCTC[A/G]TAAAATATTGATAAA | 114792 |
| rs769214461 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130131 | GCGGCCTGAGGTACC[C/T]AATGATTATCATCAC | 114792 |
| rs769218547 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018362 | GACACCAAGGCAGGC[A/G]GATCGCCTGAGGTCA | 114792 |
| rs769232999 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921933 | AAGTATATTAAGAGG[C/T]AAGCTGAGAAAAACA | 114792 |
| rs769235324 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943899 | GATTTATTTAGCCAG[A/C]TTCTTCAGATCTAGA | 114792 |
| rs769249191 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97095415 | ATCTCATGTAAGTTT[C/T]AGGCAATGTAGAGGG | 114792 |
| rs769295506 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97104130 | CTCTTATCCTATCTT[G/T]ATTTTCTCTTCATCT | 114792 |
| rs769300175 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039506 | GACTATAGTTTACAG[C/T]AATCTATTGTACACT | 114792 |
| rs769314000 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931642 | TTTACTAGTTGGTAA[C/G]ATTACTTGAGATACC | 114792 |
| rs769315216 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96946788 | CATCTTTCCCTTTAC[G/T]ATTCCTCTGGATTGG | 114792 |
| rs769348873 | in-del | -/TATTTATA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96953785 | TGACAATCTAAATGT[-/TATTTATA]TATTTATATAATCAA | 114792 |
| rs769388517 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97081136 | AGGACTGCATAGGGA[A/G]GCCCCAGGGTTGGTG | 114792 |
| rs769399565 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126279 | TCTTTGGTCCCATAT[C/G]CTTGATATTTTATTA | 114792 |
| rs769404222 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97011811 | ACTAAGGAAATAATG[A/G]TTGTTATTCAAGCTG | 114792 |
| rs769408035 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97101379 | AGGAACATATCAAGA[C/T]ACTCAAAATCAAGAA | 114792 |
| rs769422468 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97127959 | CCTGTACCTTCTTTT[A/G]TCTACATTTCATGTA | 114792 |
| rs769431914 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915964 | AACCATTATCATTAG[C/T]GACAGAAAGTGTTAA | 114792 |
| rs769435546 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971573 | TATGGCTGATCAAAT[C/G]GTTGCTCCCTGGCAT | 114792 |
| rs769445265 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97094162 | CAACACAAATGACCC[G/T]GTGAGTCCTTTTTCT | 114792 |
| rs769514615 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021577 | TCAGTCTACTGATTA[A/G]CATGTTAATTTCATC | 114792 |
| rs769551137 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131762 | GGGAGGCAACGCTGG[A/G]AATCTAATCAGAGGT | 114792 |
| rs769551142 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97015669 | AGGAAAACCCATTTT[C/G]TGGGGAGACGTTCAA | 114792 |
| rs769583770 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928954 | TTGAAAAGCTGTACT[C/T]AAATCTAGACAGAAG | 114792 |
| rs769597947 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019924 | AGCTGGAACTACAGG[C/T]GCCCATCACCACTCC | 114792 |
| rs769599166 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97120045 | AGAGTGAAATTGAAG[A/G]TGTAGGGAGGAGGGG | 114792 |
| rs769603921 | in-del | -/AGAT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96992845 | TGCCCAGGGACTGCC[-/AGAT]AGATATAAAGTAGAA | 114792 |
| rs769607328 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990218 | TTATCTCTGTGTGCT[A/G]ATGTTCCTTTCACAG | 114792 |
| rs769616976 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141922 | ATTAGGTAATGACTA[A/G]GGTACTTTTCATACT | 114792 |
| rs769629082 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96959522 | TTCATTTGTATTTGC[A/G]TGTGTTTTAATCTCT | 114792 |
| rs769666493 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97033421 | TTTTCTTTATCCATT[C/T]ATCCGTTGAGGGACA | 114792 |
| rs769672062 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97032005 | ATAATTGTATTTAAA[C/T]CTATAACAACCCTGT | 114792 |
| rs769674219 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97072536 | TACACAGGGCCTGTC[C/T]TTATTATGAAATGTG | 114792 |
| rs769705033 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96960374 | AGAAGCCCAAAACCC[C/T]TTTACCTTTGATTAT | 114792 |
| rs769718389 | snp | C/T | 1.6669e-05 | 0.00288691 | intron-variant | KLHL32 | GRCh38.p7 | 6:96967105 | CCTGTAGGATATGTC[C/T]TCACATGCCGTAGTG | 114792 |
| rs769718548 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96902585 | TTGTGCAGAGCTCTT[C/T]AGTTTAATTAGATCC | 114792 |
| rs769745126 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97019853 | GGCGCGATCTTGGCT[C/T]ACTGCAATCTCTGCC | 114792 |
| rs769759204 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073422 | ATAAATAATAAAATA[A/G]TGCTTTGACAAAAGC | 114792 |
| rs769779122 | snp | A/G | 8.2648e-05 | 0.00642784 | intron-variant, synonymous-codon, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114517 | GATATCAGGTAGAAC[A/G]TACCTCATGTTGGAT | 114792 |
| rs769798976 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97036601 | TCACCTGAGGTGTGA[C/T]GATGGGTGGGCTGTG | 114792 |
| rs769811230 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96952229 | TAAATAATTATCTTA[C/T]TTGTTTTTATTAATG | 114792 |
| rs769815237 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97065795 | GTTACCTCTTAGGTA[A/G]TTTACAAAGCTCTTT | 114792 |
| rs769825949 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97077002 | ACCCACTGTATATCA[A/G]TCAAAACTTGCTAGG | 114792 |
| rs769837974 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007898 | GCTGTCCACAACACC[C/G]CGATGAGGGCTGCCC | 114792 |
| rs769853564 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97069886 | AGATTATCATTTTTA[A/G]TTAAGTAATACTACA | 114792 |
| rs769868269 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97085919 | TTTTCACATTGTGTC[A/G]CTCCCTTGTCTAGAG | 114792 |
| rs769923399 | snp | C/T | 1.64754e-05 | 0.00287009 | upstream-variant-2KB, synonymous-codon | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96897730 | GACAGAGGGCTTCAT[C/T]TTGCTGATTTCCCGT | 114792 |
| rs769925199 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977144 | CTTCTTGTGATTCAC[A/T]TGGTGAGCAAAGGAT | 114792 |
| rs769958523 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97117926 | AATAAGACAAATGTT[A/G]TTGCATTTACTCAAA | 114792 |
| rs769977960 | in-del | -/TT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96901331 | CCTCCTGGATGCCTT[-/TT]TTTTTTTTTTACTTT | 114792 |
| rs769997673 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114055 | TGGGAAAAAGCGCGA[A/G]GTCTGCAAGGTCAAG | 114792 |
| rs770014745 | snp | G/T | 1.6989e-05 | 0.00291449 | intron-variant | KLHL32 | GRCh38.p7 | 6:97139100 | TTTGATACACAAGCT[G/T]CTTCTCTTCCTCTTT | 114792 |
| rs770020066 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075592 | AAGGCTATTAAAAGG[C/T]TTGGATTTTGTTTAT | 114792 |
| rs770034530 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97103304 | CTGCAAGCTCCGCTT[C/G]CCAGGTTCATGCGAT | 114792 |
| rs770051417 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135452 | CTGGGATTTCAGGCA[A/T]GTGCCACCATGCCCA | 114792 |
| rs770058629 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97097277 | GCTGTCACTCCAGCC[A/G]TCTGTTGATTGAAAA | 114792 |
| rs770070070 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96898275 | AAGTTGTTTCACAGG[A/G]CAATGCCACCAAAGA | 114792 |
| rs770129607 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930795 | CACTGTTCCCTCTTT[C/T]ATGCAGCTCCTGGAG | 114792 |
| rs770149360 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96979063 | ATCTTTGTCAGATGC[A/G]TAGTTTGCAAAATAT | 114792 |
| rs770184160 | snp | C/T | | | upstream-variant-2KB, intron-variant | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896098 | CTTTTCCCATAATTA[C/T]GGTCACATTGTTGCT | 114792 |
| rs770188068 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96962230 | CTAGCAACTTTGAAA[C/T]ATTTTAATAAAAATA | 114792 |
| rs770210498 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089575 | CTTGAGGTCAGGAAT[G/T]TGAAACCAGCCTGCC | 114792 |
| rs770233418 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97115502 | GAATAATGAACCCCA[A/T]GTACCCACAACCCAA | 114792 |
| rs770242733 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058972 | GTTTTTGAGGTAGAC[A/G]TCATTATTTTCACTG | 114792 |
| rs770250486 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96957422 | TTTGTCATATTATAA[A/T]GTAATATGTTATTTA | 114792 |
| rs770275485 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97031982 | ACATATTATGCCTAA[C/G]ATTAAGCATAATTGT | 114792 |
| rs770280524 | in-del | -/AG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97110830 | GGGCAAACTCAAAAC[-/AG]AAGCCTGCTGCTGTT | 114792 |
| rs770290489 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082201 | AAGAGACAGGACTGG[C/T]GATTGACTAGATGTA | 114792 |
| rs770292790 | snp | A/T | 0.000116483 | 0.00763073 | intron-variant | KLHL32 | GRCh38.p7 | 6:97132632 | ATTTTTTTTCTTTTT[A/T]TTCAATTCTCTTTAC | 114792 |
| rs770293819 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046854 | ATTCACTGACATGTA[A/G]TCTTTATCCGTGATA | 114792 |
| rs770315864 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97041548 | GGTTAATTTGCACGG[C/T]GTGACCAGCCTTGGC | 114792 |
| rs770329142 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97029801 | GTAACCAAAATGTAA[G/T]AAAGGCTAATAACCA | 114792 |
| rs770339684 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977956 | TTCACACACCCTCAC[C/T]CACATTGTCAGGTAT | 114792 |
| rs770367187 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97128723 | TGATTAGTATTCACA[A/T]GCTAGCTTATTAGGA | 114792 |
| rs770370710 | in-del | -/TAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97126753 | ATATATAAAATATCT[-/TAA]TAATTTTTATGTTGA | 114792 |
| rs770371765 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96934392 | CTTATTCCTACCTTC[C/T]GAGGACCAGCCAGGC | 114792 |
| rs770380434 | snp | G/T | 1.68789e-05 | 0.00290503 | intron-variant | KLHL32 | GRCh38.p7 | 6:97113775 | CATCTCACTTCCCTC[G/T]GTTTCAGCTAGCTGT | 114792 |
| rs770386173 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062214 | ACTGTCTTTGTGTTT[C/G]CTATTAGTGAGCCTT | 114792 |
| rs770405493 | in-del | -/TTGTTGCCA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993599 | AAGTAGGGGAACATT[-/TTGTTGCCA]TTGTTGCACCCTTCT | 114792 |
| rs770415216 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96921194 | CGATATTCTTTCTTA[C/T]AGTTAGGGGCTATTT | 114792 |
| rs770421746 | snp | G/T | 0.000363835 | 0.0134828 | intron-variant, synonymous-codon, utr-variant-5-prime | KLHL32 | GRCh38.p7 | 6:97105502 | GTGCCCTGGCTTACC[G/T]CAATGGGATGACAAG | 114792 |
| rs770433231 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97010086 | CTACTGGGTTTTTCC[C/T]TAGACTTAGGGTAAG | 114792 |
| rs770448391 | in-del | -/AATG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96928259 | GGTATGATTATATTA[-/AATG]AAAATCCTTATAGCT | 114792 |
| rs770454470 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106756 | TCAAAAAAAAAAAAA[A/G]TTAAATGTGAAATAT | 114792 |
| rs770469463 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97030147 | CCTGTGTTCAGAGTA[A/T]CTCCAAAGCTGCACA | 114792 |
| rs770479934 | in-del | -/TT/TTT/TTTT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135299 | AGACAAATTTGTTAA[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT | 114792 |
| rs770542822 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97093551 | ACGTTTTTATATATT[A/G]CTCTGTAATGAGTGA | 114792 |
| rs770577272 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96993659 | TCTGAGATTTTTACC[A/C]TACTTGCAAGCTAAC | 114792 |
| rs770590281 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97021308 | CAACAGGTAGTTTTT[C/G]AACAATGGTGTAGTT | 114792 |
| rs770595703 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900704 | ATTCTGCGTTCTCCA[A/G]AGGATTACAGTAGCT | 114792 |
| rs770608419 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96966156 | AAAATAAAATTGAGA[A/C]AGAAGGAAGCCTATT | 114792 |
| rs770628381 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96977363 | CTTAACGAGTGTGAT[A/G]GTCTGCTTCATATAT | 114792 |
| rs770629977 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96958426 | AGGCAAAAAGGAGGG[G/T]TAGAAAGTTCTAAAC | 114792 |
| rs770661379 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96976547 | TGTTAAAATTTAAAA[A/G]TCTTTAAGTATATGT | 114792 |
| rs770684466 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97131557 | ACGGTGAACAACTTA[C/T]CCCTCATGTTTCTTT | 114792 |
| rs770686383 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96915880 | CCCTCCCCCATCGGC[C/T]TAAAAGCAGGACATA | 114792 |
| rs770687686 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970815 | CAAGTTCATTTTAAA[-/G]TGTTTATAAATTATA | 114792 |
| rs770714238 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97083969 | AAGCCCATCTGCCCC[A/G]AAAGGAGGAGTGTGT | 114792 |
| rs770726627 | in-del | -/TTA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96965456 | CATATCAAGTTAGAC[-/TTA]TTAGTTAGATGCCAT | 114792 |
| rs770735719 | snp | C/G | 1.67579e-05 | 0.00289459 | intron-variant, missense, utr-variant-3-prime | KLHL32 | GRCh38.p7 | 6:97114546 | ATTTATCAAAACACA[C/G]TTTCATTGTGGTATA | 114792 |
| rs770742734 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96971325 | CCATGAACATCAAAC[C/T]CTATAGGATTTCTGT | 114792 |
| rs770772339 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118345 | AGACAAAGGCCGGGT[A/G]CAGTGGCTCACGCCA | 114792 |
| rs770775188 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96970128 | AAACTTCATCTGAGT[G/T]CTCCTTGGGCTCCAA | 114792 |
| rs770781124 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97082777 | GGTCAGTCATATAGA[A/T]GTGGAAGGCATTAAC | 114792 |
| rs770781769 | in-del | -/TTTTTTTTTTTTTTTTGGCAGC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911850 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTGGCAGC]TGGCAGCTGCCACTC | 114792 |
| rs770790410 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96927239 | AAGGCCAAGAAGTGG[A/G]GAAAAACTCAGTTGA | 114792 |
| rs770792926 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013476 | AAAATAGTTACACCA[A/G]TGCTAGGTGGTGTTT | 114792 |
| rs770802221 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071672 | CCATCATCTTTCTAG[G/T]CACTCAAACCTTGGC | 114792 |
| rs770825999 | in-del | -/ACAC | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96943041 | ATGCTCCCTCTACAC[-/ACAC]ACACACACACACACA | 114792 |
| rs770829519 | snp | C/T | 1.65976e-05 | 0.00288072 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064760 | TGCTCATACACCCTT[C/T]ACATTCCTTTCCCCA | 114792 |
| rs770832531 | in-del | -/ATGCT | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97004018 | CTAATTCTGTGAAGA[-/ATGCT]ATTGGTTGTTTTATA | 114792 |
| rs770849608 | snp | C/T | | | intron-variant, upstream-variant-2KB | KLHL32 | GRCh38.p7 | 6:97039868 | GAAAGAAAAGAAAAT[C/T]GCTCGAAGAGAATAA | 114792 |
| rs770877004 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97130238 | TTTAATCTTCACAAT[A/G]GGCTTATCAGGTAGG | 114792 |
| rs770904841 | in-del | -/TG | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96942009 | GACTGGCATATGTAC[-/TG]TGTATATATAGTAAC | 114792 |
| rs770917377 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914297 | TTTCAAGCCTCTGTA[C/T]TTGAGATAATTTATG | 114792 |
| rs770919499 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97014499 | AAAAATGTTTCAAGA[A/G]TACTACAATAGTGAA | 114792 |
| rs770948365 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96916904 | ATCTAAAAATTATGT[G/T]TGGTGAAATATAATC | 114792 |
| rs770950542 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97089460 | TGTTTCTTACTTTTA[A/G]TGAGAACTTATTATT | 114792 |
| rs770959185 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97075365 | AAAATATGCCTATAT[A/C]TCTCTGTATGTTTAT | 114792 |
| rs770984172 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96931440 | GCCTGAGCAGTATAT[C/T]GTAGGATCCCATAGA | 114792 |
| rs770990285 | snp | A/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97046713 | TGCAGTTTACTTGAG[A/T]TTGTTGAACAGCTGC | 114792 |
| rs770995174 | in-del | -/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97138617 | GAACAGGAAAGAACT[-/G]GGGAAAACCTTCCAG | 114792 |
| rs770996865 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97098423 | TACCTAGCCTGGGAC[A/G]TTTTTTCTCACATGT | 114792 |
| rs771000427 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97073726 | ATAAAAACTGTGTAT[C/T]TATTTAAAAGAAAAA | 114792 |
| rs771001425 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96904945 | CATTTATAACAATTC[C/T]CTGTCTTCTTTCTTC | 114792 |
| rs771009965 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96973436 | AATACATTTATTTAA[C/T]ATTTAAGGTGATATA | 114792 |
| rs771012882 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97106683 | TGGGAGGCAGAAGTC[A/G]TAGTGAGCTGAGATT | 114792 |
| rs771028449 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96930706 | TTAGTGATGCAGTAC[A/G]CTGCTTAGATGGGCT | 114792 |
| rs771039503 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96961925 | TGAACTAGACAAAAG[C/G]TGCCCCCTAGTTTCT | 114792 |
| rs771065064 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96917881 | CTCTCTGAGACTGAG[G/T]TCTATGCGTAGAAAA | 114792 |
| rs771070561 | snp | C/G | 1.64955e-05 | 0.00287184 | missense, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97139245 | GCCCTAACCTTCAAA[C/G]TCTTCAAGTGCCTCA | 114792 |
| rs771072710 | in-del | -/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97112833 | AACAAAATGAAACAA[-/T]ATTCTTTATTATTTA | 114792 |
| rs771093264 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96990603 | TGTGTGTCCTCTCCA[A/G]CTTGGAGGCAGCAGA | 114792 |
| rs771105038 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97137133 | CTAGCCAAAACCCCA[C/T]CGGGGTTTTCCCTTT | 114792 |
| rs771107752 | in-del | -/GGCTTACCTCAA | 0.00012119 | 0.00778334 | intron-variant, cds-indel | KLHL32 | GRCh38.p7 | 6:97105494 | GGAGACTGGTGCCCT[-/GGCTTACCTCAA]TGGGATGACAAGACT | 114792 |
| rs771109190 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97007723 | AGGTACAGTCAACTG[A/G]CCTCATTTGTGGAAG | 114792 |
| rs771151599 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97058918 | TATAGACACACACAA[C/T]TGTAATGATACACAA | 114792 |
| rs771160622 | snp | G/T | 3.29489e-05 | 0.00405874 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114070 | GGTCTGCAAGGTCAA[G/T]GAACTTCGGTACTTC | 114792 |
| rs771179544 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114415 | AGTTGAGCGATATTG[C/T]CCCAAGAAGAACAAA | 114792 |
| rs771180527 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96987855 | CAAGAAATGGGGAAA[G/T]GATTCCCTATTTAAT | 114792 |
| rs771195088 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97123120 | GAGGTATTTTTTGTC[A/G]TTAAAAAAAAAATTA | 114792 |
| rs771211010 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97135246 | TTTGGCAAATACTGC[A/G]TTTATTCCTTTGGCT | 114792 |
| rs771226125 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97062123 | CGTATGGGTTTTTCA[C/T]GTGCAGGCTTCTGGA | 114792 |
| rs771228841 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97028370 | CTTGCTTCTTACACA[C/T]ACCCAGCACAGCTTT | 114792 |
| rs771243329 | snp | A/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96910824 | GATAAAATAAGAGAA[A/C]CATAAAACTAGAAGC | 114792 |
| rs771250392 | snp | C/G | 0.000115362 | 0.00759393 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97114191 | GTGGCAGTCATGGGG[C/G]ACTTCCTGTTTGTGG | 114792 |
| rs771278294 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96911018 | TAATAATACATATCT[A/G]TATCTTAAGTATCTT | 114792 |
| rs771313312 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97087921 | AAAATGTGTTGTATG[C/T]AGGCCACGGTAATCA | 114792 |
| rs771333366 | snp | A/G | 3.62339e-05 | 0.00425624 | intron-variant | KLHL32 | GRCh38.p7 | 6:97064619 | TATTTTTGTTAACAA[A/G]CAAAACAGATTTTGC | 114792 |
| rs771350393 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97006608 | TCTATATACTTAAAT[G/T]TGTTTTTGTGGTGAC | 114792 |
| rs771350479 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97017405 | ATTGGGAGAGTTGCT[G/T]CCCTTCTCTAACTAT | 114792 |
| rs771351147 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97102340 | TGGGGGGTGTTGTGA[C/T]CCACATGAGGTCACT | 114792 |
| rs771356818 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96955566 | GCATTCAGTGCAAAC[A/G]TTTGAATGGATATGT | 114792 |
| rs771368041 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96936914 | TGTCTTACCTCCTTC[A/G]GGTCTTTGCTCAAAT | 114792 |
| rs771390159 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97039358 | CATGAAGACATAGAG[C/T]AGATTGGTGGTTACC | 114792 |
| rs771398838 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97010946 | AGAGGAAAGCAAATA[C/T]CAGTGGATGTGTGGA | 114792 |
| rs771406775 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97086502 | CCTGAAAGAATGGCT[A/G]TTATCACTGCATGTA | 114792 |
| rs771417024 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96944279 | CACTATCTAAAAGAG[C/T]CTAGGCAAGAATAAA | 114792 |
| rs771419101 | snp | G/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97060104 | TGCTCAAATCCTTCA[G/T]TCCACTGTACACATA | 114792 |
| rs771421237 | snp | A/G | 1.65277e-05 | 0.00287464 | upstream-variant-2KB, missense | KLHL32, NDUFAF4 | GRCh38.p7 | 6:96896779 | CTTTGGAATCAACAT[A/G]CACATCTTTTAGAAA | 114792 |
| rs771429152 | in-del | -/AGAA | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97013450 | TAAGTGGCAGTGCTT[-/AGAA]AGGAATAAAAATAGT | 114792 |
| rs771443310 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96914091 | GATCCTGGCTTTGAA[A/G]AAAGCGGGGGAATCT | 114792 |
| rs771449749 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97118438 | AGCCTGGCCAGCATG[A/G]TGAAACCCCATCTCT | 114792 |
| rs771466310 | snp | A/G | 1.64895e-05 | 0.00287132 | missense, intron-variant, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:97130914 | ACAACATAGACACTG[A/G]CCAGTGGACACGTTG | 114792 |
| rs771477938 | in-del | -/C | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97027754 | CTAGGGATCAGTCCT[-/C]CCCATGCTGGGATTT | 114792 |
| rs771486549 | snp | G/T | 1.66214e-05 | 0.00288278 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | KLHL32 | GRCh38.p7 | 6:96976060 | CAATGACAGTGTCCT[G/T]GCAGCGCTGAATCAG | 114792 |
| rs771494575 | snp | C/T | | | intron-variant | KLHL32 | GRCh38.p7 | 6:96900492 | AACGTGCTCAGCACA[C/T]GTGGTGGTATTGTTA | 114792 |
| rs771500115 | snp | C/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97071564 | TGTATGTTCAGCCAG[C/G]ATTTCACTTGATATG | 114792 |
| rs771510094 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | MMS22L, KLHL32 | GRCh38.p7 | 6:97141684 | ATTGTATTTGTAATG[C/T]AAATTATTATACTAA | 114792 |
| rs771512788 | snp | A/G | | | intron-variant | KLHL32 | GRCh38.p7 | 6:97018667 | TCAGAAAAAATATTA[A/G]TCAGATGCTAACAAA | 114792 |